GS follow link to MSigDB | GS DETAILS | SIZE | ES | NES | NOM p-val | FDR q-val | FWER p-val | RANK AT MAX | LEADING EDGE | |
---|---|---|---|---|---|---|---|---|---|---|
1 | PEPTIDYL-PROLINE HYDROXYLATION | Details ... | 17 | -0.63 | -1.92 | 0.002 | 1.000 | 0.403 | 5067 | tags=47%, list=9%, signal=52% |
2 | POSITIVE REGULATION OF NUCLEASE ACTIVITY | Details ... | 25 | -0.57 | -1.84 | 0.002 | 1.000 | 0.620 | 12208 | tags=56%, list=22%, signal=72% |
3 | REGULATION OF ISOTYPE SWITCHING | Details ... | 17 | -0.64 | -1.83 | 0.000 | 1.000 | 0.630 | 5072 | tags=53%, list=9%, signal=58% |
4 | PEPTIDYL-SERINE AUTOPHOSPHORYLATION | Details ... | 15 | -0.65 | -1.83 | 0.000 | 1.000 | 0.645 | 8533 | tags=53%, list=16%, signal=63% |
5 | OOCYTE DIFFERENTIATION | Details ... | 12 | -0.69 | -1.81 | 0.004 | 1.000 | 0.673 | 1978 | tags=42%, list=4%, signal=43% |
6 | SULFIDE OXIDATION | Details ... | 6 | -0.84 | -1.76 | 0.002 | 1.000 | 0.731 | 8576 | tags=100%, list=16%, signal=119% |
7 | SULFIDE OXIDATION, USING SULFIDE:QUINONE OXIDOREDUCTASE | Details ... | 6 | -0.84 | -1.76 | 0.002 | 1.000 | 0.731 | 8576 | tags=100%, list=16%, signal=119% |
8 | REGULATION OF MITOPHAGY | Details ... | 76 | -0.48 | -1.75 | 0.000 | 1.000 | 0.749 | 18494 | tags=61%, list=34%, signal=91% |
9 | MACROMOLECULE DEPALMITOYLATION | Details ... | 6 | -0.79 | -1.75 | 0.002 | 1.000 | 0.753 | 9498 | tags=83%, list=17%, signal=101% |
10 | IRON-SULFUR CLUSTER ASSEMBLY | Details ... | 13 | -0.72 | -1.74 | 0.000 | 1.000 | 0.754 | 15238 | tags=100%, list=28%, signal=139% |
11 | METALLO-SULFUR CLUSTER ASSEMBLY | Details ... | 13 | -0.72 | -1.74 | 0.000 | 1.000 | 0.754 | 15238 | tags=100%, list=28%, signal=139% |
12 | PROTEIN HYDROXYLATION | Details ... | 24 | -0.55 | -1.73 | 0.000 | 1.000 | 0.773 | 5067 | tags=42%, list=9%, signal=46% |
13 | REGULATION OF TORC1 SIGNALING | Details ... | 15 | -0.58 | -1.73 | 0.006 | 1.000 | 0.774 | 7264 | tags=47%, list=13%, signal=54% |
14 | RESPONSE TO MISFOLDED PROTEIN | Details ... | 40 | -0.53 | -1.72 | 0.004 | 1.000 | 0.785 | 15267 | tags=68%, list=28%, signal=94% |
15 | NEGATIVE REGULATION OF MACROAUTOPHAGY | Details ... | 35 | -0.52 | -1.71 | 0.002 | 1.000 | 0.786 | 14677 | tags=66%, list=27%, signal=90% |
16 | MITOCHONDRIAL ATP SYNTHESIS COUPLED PROTON TRANSPORT | Details ... | 40 | -0.60 | -1.70 | 0.046 | 1.000 | 0.790 | 18490 | tags=83%, list=34%, signal=125% |
17 | POSITIVE REGULATION OF RUFFLE ASSEMBLY | Details ... | 14 | -0.63 | -1.70 | 0.018 | 1.000 | 0.799 | 7877 | tags=57%, list=14%, signal=67% |
18 | OOCYTE DEVELOPMENT | Details ... | 11 | -0.66 | -1.70 | 0.010 | 1.000 | 0.800 | 1255 | tags=36%, list=2%, signal=37% |
19 | POSITIVE REGULATION OF ISOTYPE SWITCHING | Details ... | 12 | -0.65 | -1.69 | 0.008 | 1.000 | 0.800 | 5072 | tags=50%, list=9%, signal=55% |
20 | ACTIVATION OF SIGNALING PROTEIN ACTIVITY INVOLVED IN UNFOLDED PROTEIN RESPONSE | Details ... | 16 | -0.58 | -1.69 | 0.011 | 1.000 | 0.807 | 10798 | tags=50%, list=20%, signal=62% |
21 | NUCLEOSOME DISASSEMBLY | 49 | -0.49 | -1.69 | 0.002 | 1.000 | 0.808 | 15415 | tags=57%, list=28%, signal=80% | |
22 | CHROMATIN DISASSEMBLY | 49 | -0.49 | -1.69 | 0.002 | 1.000 | 0.808 | 15415 | tags=57%, list=28%, signal=80% | |
23 | PROTEIN-DNA COMPLEX DISASSEMBLY | 49 | -0.49 | -1.69 | 0.002 | 1.000 | 0.808 | 15415 | tags=57%, list=28%, signal=80% | |
24 | POSITIVE REGULATION OF ERAD PATHWAY | 31 | -0.54 | -1.68 | 0.000 | 1.000 | 0.809 | 15185 | tags=65%, list=28%, signal=89% | |
25 | ENERGY COUPLED PROTON TRANSPORT, DOWN ELECTROCHEMICAL GRADIENT | 41 | -0.58 | -1.68 | 0.048 | 1.000 | 0.809 | 18490 | tags=80%, list=34%, signal=122% | |
26 | ATP SYNTHESIS COUPLED PROTON TRANSPORT | 41 | -0.58 | -1.68 | 0.048 | 1.000 | 0.809 | 18490 | tags=80%, list=34%, signal=122% | |
27 | BASE-EXCISION REPAIR, AP SITE FORMATION | 19 | -0.54 | -1.68 | 0.011 | 1.000 | 0.810 | 16304 | tags=68%, list=30%, signal=97% | |
28 | PEPTIDYL-DIPHTHAMIDE METABOLIC PROCESS | 14 | -0.67 | -1.68 | 0.011 | 1.000 | 0.811 | 7519 | tags=71%, list=14%, signal=83% | |
29 | PEPTIDYL-DIPHTHAMIDE BIOSYNTHETIC PROCESS FROM PEPTIDYL-HISTIDINE | 14 | -0.67 | -1.68 | 0.011 | 1.000 | 0.811 | 7519 | tags=71%, list=14%, signal=83% | |
30 | POSITIVE REGULATION OF NEUROTRANSMITTER SECRETION | 11 | -0.63 | -1.67 | 0.004 | 1.000 | 0.814 | 8298 | tags=64%, list=15%, signal=75% | |
31 | MITOCHONDRIAL RESPIRATORY CHAIN COMPLEX ASSEMBLY | 115 | -0.50 | -1.67 | 0.037 | 1.000 | 0.817 | 16184 | tags=66%, list=30%, signal=94% | |
32 | POSITIVE REGULATION OF ANOIKIS | 7 | -0.75 | -1.67 | 0.006 | 1.000 | 0.817 | 8233 | tags=71%, list=15%, signal=84% | |
33 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO MITOCHONDRION | 117 | -0.49 | -1.67 | 0.034 | 1.000 | 0.818 | 15809 | tags=64%, list=29%, signal=90% | |
34 | REGULATION OF AUTOPHAGOSOME MATURATION | 14 | -0.66 | -1.66 | 0.004 | 1.000 | 0.822 | 13374 | tags=86%, list=24%, signal=113% | |
35 | PROTEIN LOCALIZATION TO MITOCHONDRION | 124 | -0.49 | -1.66 | 0.026 | 1.000 | 0.824 | 15809 | tags=65%, list=29%, signal=91% | |
36 | REGULATION OF IMMUNOGLOBULIN PRODUCTION | 34 | -0.52 | -1.66 | 0.012 | 1.000 | 0.825 | 5072 | tags=41%, list=9%, signal=45% | |
37 | HISTONE H4-K12 ACETYLATION | 6 | -0.77 | -1.65 | 0.002 | 1.000 | 0.829 | 12707 | tags=100%, list=23%, signal=130% | |
38 | CALCINEURIN-NFAT SIGNALING CASCADE | 13 | -0.60 | -1.64 | 0.011 | 1.000 | 0.834 | 9654 | tags=54%, list=18%, signal=65% | |
39 | REGULATION OF NUCLEASE ACTIVITY | 43 | -0.47 | -1.64 | 0.006 | 1.000 | 0.834 | 15284 | tags=56%, list=28%, signal=77% | |
40 | HEME BIOSYNTHETIC PROCESS | 31 | -0.55 | -1.64 | 0.015 | 1.000 | 0.838 | 17692 | tags=74%, list=32%, signal=110% | |
41 | AUTOPHAGOSOME MATURATION | 26 | -0.57 | -1.63 | 0.004 | 1.000 | 0.841 | 13625 | tags=69%, list=25%, signal=92% | |
42 | VACUOLE FUSION | 26 | -0.57 | -1.63 | 0.004 | 1.000 | 0.841 | 13625 | tags=69%, list=25%, signal=92% | |
43 | ELECTRON TRANSPORT CHAIN | 210 | -0.49 | -1.63 | 0.064 | 1.000 | 0.841 | 16220 | tags=64%, list=30%, signal=91% | |
44 | RESPIRATORY ELECTRON TRANSPORT CHAIN | 210 | -0.49 | -1.63 | 0.064 | 1.000 | 0.841 | 16220 | tags=64%, list=30%, signal=91% | |
45 | NADH DEHYDROGENASE COMPLEX ASSEMBLY | 102 | -0.49 | -1.63 | 0.043 | 1.000 | 0.843 | 16184 | tags=67%, list=30%, signal=95% | |
46 | MITOCHONDRIAL RESPIRATORY CHAIN COMPLEX I ASSEMBLY | 102 | -0.49 | -1.63 | 0.043 | 1.000 | 0.843 | 16184 | tags=67%, list=30%, signal=95% | |
47 | MITOCHONDRIAL RESPIRATORY CHAIN COMPLEX I BIOGENESIS | 102 | -0.49 | -1.63 | 0.043 | 1.000 | 0.843 | 16184 | tags=67%, list=30%, signal=95% | |
48 | REGULATION OF CD8-POSITIVE, ALPHA-BETA T CELL ACTIVATION | 28 | -0.56 | -1.63 | 0.014 | 1.000 | 0.843 | 7829 | tags=46%, list=14%, signal=54% | |
49 | RIBOSOMAL SMALL SUBUNIT BIOGENESIS | 36 | -0.60 | -1.63 | 0.066 | 1.000 | 0.845 | 17707 | tags=83%, list=32%, signal=123% | |
50 | POSITIVE REGULATION OF SUBSTRATE ADHESION-DEPENDENT CELL SPREADING | 58 | -0.45 | -1.63 | 0.004 | 1.000 | 0.845 | 15032 | tags=55%, list=27%, signal=76% | |
51 | POSITIVE REGULATION OF ENDOPLASMIC RETICULUM UNFOLDED PROTEIN RESPONSE | 30 | -0.49 | -1.62 | 0.015 | 1.000 | 0.845 | 12211 | tags=53%, list=22%, signal=69% | |
52 | NEGATIVE REGULATION OF RETINOIC ACID RECEPTOR SIGNALING PATHWAY | 17 | -0.57 | -1.62 | 0.017 | 1.000 | 0.845 | 21860 | tags=82%, list=40%, signal=137% | |
53 | PROTEIN TARGETING TO MITOCHONDRION | 108 | -0.48 | -1.62 | 0.051 | 1.000 | 0.850 | 15809 | tags=63%, list=29%, signal=88% | |
54 | REGULATION OF GOLGI ORGANIZATION | 16 | -0.55 | -1.62 | 0.009 | 1.000 | 0.854 | 18060 | tags=75%, list=33%, signal=112% | |
55 | CELLULAR RESPONSE TO MISFOLDED PROTEIN | 31 | -0.55 | -1.62 | 0.007 | 1.000 | 0.854 | 15267 | tags=71%, list=28%, signal=98% | |
56 | REGULATION OF RUFFLE ASSEMBLY | 32 | -0.47 | -1.61 | 0.015 | 1.000 | 0.858 | 9775 | tags=41%, list=18%, signal=49% | |
57 | VIRION ASSEMBLY | 73 | -0.52 | -1.61 | 0.034 | 1.000 | 0.859 | 16542 | tags=71%, list=30%, signal=102% | |
58 | RESPIRATORY CHAIN COMPLEX IV ASSEMBLY | 23 | -0.54 | -1.61 | 0.021 | 1.000 | 0.861 | 16995 | tags=74%, list=31%, signal=107% | |
59 | RRNA PROCESSING | 124 | -0.48 | -1.61 | 0.029 | 1.000 | 0.862 | 17707 | tags=68%, list=32%, signal=100% | |
60 | NUCLEOSIDE TRIPHOSPHATE BIOSYNTHETIC PROCESS | 81 | -0.48 | -1.61 | 0.048 | 1.000 | 0.862 | 18592 | tags=65%, list=34%, signal=99% | |
61 | MITOCHONDRIAL TRANSLATION | 198 | -0.47 | -1.60 | 0.068 | 1.000 | 0.862 | 16149 | tags=64%, list=30%, signal=91% | |
62 | REGULATION OF CELLULAR AMINO ACID METABOLIC PROCESS | 114 | -0.47 | -1.60 | 0.062 | 1.000 | 0.863 | 19835 | tags=69%, list=36%, signal=109% | |
63 | REGULATION OF IRE1-MEDIATED UNFOLDED PROTEIN RESPONSE | 29 | -0.50 | -1.60 | 0.015 | 1.000 | 0.866 | 17716 | tags=66%, list=32%, signal=97% | |
64 | MITOCHONDRIAL TRANSMEMBRANE TRANSPORT | 102 | -0.48 | -1.60 | 0.062 | 1.000 | 0.867 | 20106 | tags=72%, list=37%, signal=113% | |
65 | PORPHYRIN-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 33 | -0.52 | -1.59 | 0.035 | 1.000 | 0.870 | 17692 | tags=70%, list=32%, signal=103% | |
66 | TETRAPYRROLE BIOSYNTHETIC PROCESS | 33 | -0.52 | -1.59 | 0.035 | 1.000 | 0.870 | 17692 | tags=70%, list=32%, signal=103% | |
67 | OLIGODENDROCYTE DEVELOPMENT | 25 | -0.55 | -1.59 | 0.015 | 1.000 | 0.871 | 18817 | tags=76%, list=34%, signal=116% | |
68 | RIBONUCLEOSIDE TRIPHOSPHATE BIOSYNTHETIC PROCESS | 62 | -0.50 | -1.59 | 0.066 | 1.000 | 0.871 | 18490 | tags=69%, list=34%, signal=105% | |
69 | PEPTIDYL-METHIONINE MODIFICATION | 19 | -0.51 | -1.59 | 0.012 | 1.000 | 0.873 | 15175 | tags=53%, list=28%, signal=73% | |
70 | REGULATION OF PROTEIN TARGETING TO MEMBRANE | 34 | -0.52 | -1.59 | 0.034 | 1.000 | 0.873 | 14953 | tags=62%, list=27%, signal=85% | |
71 | POSITIVE REGULATION OF IRE1-MEDIATED UNFOLDED PROTEIN RESPONSE | 23 | -0.50 | -1.59 | 0.023 | 1.000 | 0.874 | 9044 | tags=48%, list=17%, signal=57% | |
72 | POSITIVE REGULATION OF DNA RECOMBINATION | 13 | -0.61 | -1.59 | 0.034 | 1.000 | 0.874 | 5072 | tags=46%, list=9%, signal=51% | |
73 | DEOXYRIBONUCLEOTIDE CATABOLIC PROCESS | 35 | -0.47 | -1.58 | 0.020 | 1.000 | 0.874 | 16304 | tags=60%, list=30%, signal=85% | |
74 | DEOXYRIBOSE PHOSPHATE CATABOLIC PROCESS | 35 | -0.47 | -1.58 | 0.020 | 1.000 | 0.874 | 16304 | tags=60%, list=30%, signal=85% | |
75 | REGULATION OF T CELL CYTOKINE PRODUCTION | 50 | -0.44 | -1.58 | 0.002 | 1.000 | 0.875 | 7829 | tags=34%, list=14%, signal=40% | |
76 | SPLICEOSOMAL TRI-SNRNP COMPLEX ASSEMBLY | 18 | -0.54 | -1.58 | 0.051 | 1.000 | 0.875 | 14061 | tags=61%, list=26%, signal=82% | |
77 | ACTIN NUCLEATION | 40 | -0.52 | -1.58 | 0.021 | 1.000 | 0.875 | 16272 | tags=63%, list=30%, signal=89% | |
78 | TRNA AMINOACYLATION FOR PROTEIN TRANSLATION | 89 | -0.51 | -1.58 | 0.011 | 1.000 | 0.875 | 18230 | tags=70%, list=33%, signal=104% | |
79 | CYTOCHROME COMPLEX ASSEMBLY | 27 | -0.51 | -1.57 | 0.021 | 1.000 | 0.875 | 16995 | tags=70%, list=31%, signal=102% | |
80 | ATP BIOSYNTHETIC PROCESS | 61 | -0.50 | -1.57 | 0.068 | 1.000 | 0.876 | 18490 | tags=69%, list=34%, signal=104% | |
81 | PURINE NUCLEOSIDE TRIPHOSPHATE BIOSYNTHETIC PROCESS | 61 | -0.50 | -1.57 | 0.068 | 1.000 | 0.876 | 18490 | tags=69%, list=34%, signal=104% | |
82 | PURINE RIBONUCLEOSIDE TRIPHOSPHATE BIOSYNTHETIC PROCESS | 61 | -0.50 | -1.57 | 0.068 | 1.000 | 0.876 | 18490 | tags=69%, list=34%, signal=104% | |
83 | ORGANELLE MEMBRANE FUSION | 82 | -0.47 | -1.57 | 0.013 | 1.000 | 0.877 | 14479 | tags=57%, list=26%, signal=78% | |
84 | MITOCHONDRIAL TRANSLATIONAL INITIATION | 159 | -0.47 | -1.57 | 0.085 | 1.000 | 0.877 | 16149 | tags=64%, list=30%, signal=91% | |
85 | PEPTIDYL-HISTIDINE MODIFICATION | 17 | -0.61 | -1.57 | 0.024 | 1.000 | 0.878 | 7519 | tags=65%, list=14%, signal=75% | |
86 | NEGATIVE REGULATION OF RECEPTOR BINDING | 41 | -0.47 | -1.57 | 0.011 | 1.000 | 0.878 | 9410 | tags=41%, list=17%, signal=50% | |
87 | RRNA METABOLIC PROCESS | 132 | -0.47 | -1.57 | 0.024 | 1.000 | 0.878 | 17707 | tags=67%, list=32%, signal=98% | |
88 | DEPYRIMIDINATION | 17 | -0.52 | -1.56 | 0.024 | 1.000 | 0.879 | 16304 | tags=65%, list=30%, signal=92% | |
89 | PHOSPHATIDYLGLYCEROL BIOSYNTHETIC PROCESS | 38 | -0.49 | -1.56 | 0.011 | 1.000 | 0.882 | 20374 | tags=74%, list=37%, signal=117% | |
90 | PEPTIDYL-TYROSINE AUTOPHOSPHORYLATION | 16 | -0.56 | -1.56 | 0.039 | 1.000 | 0.883 | 11665 | tags=63%, list=21%, signal=79% | |
91 | PROTEIN COMPLEX DISASSEMBLY | 475 | -0.46 | -1.56 | 0.105 | 1.000 | 0.883 | 17321 | tags=65%, list=32%, signal=94% | |
92 | MATURATION OF 5.8S RRNA | 19 | -0.55 | -1.56 | 0.011 | 1.000 | 0.883 | 11958 | tags=63%, list=22%, signal=81% | |
93 | MITOCHONDRIAL TRANSLATIONAL ELONGATION | 166 | -0.46 | -1.56 | 0.099 | 1.000 | 0.883 | 16149 | tags=63%, list=30%, signal=89% | |
94 | POSITIVE REGULATION OF HISTONE ACETYLATION | 50 | -0.42 | -1.56 | 0.034 | 1.000 | 0.883 | 9583 | tags=40%, list=18%, signal=48% | |
95 | MITOCHONDRIAL TRANSLATIONAL TERMINATION | 163 | -0.46 | -1.56 | 0.087 | 1.000 | 0.885 | 16149 | tags=63%, list=30%, signal=89% | |
96 | REGULATION OF RETINOIC ACID RECEPTOR SIGNALING PATHWAY | 27 | -0.51 | -1.55 | 0.017 | 1.000 | 0.886 | 22614 | tags=81%, list=41%, signal=139% | |
97 | OLIGODENDROCYTE DIFFERENTIATION | 30 | -0.48 | -1.55 | 0.038 | 1.000 | 0.886 | 18817 | tags=67%, list=34%, signal=102% | |
98 | FATTY ACID BETA-OXIDATION | 83 | -0.47 | -1.55 | 0.033 | 1.000 | 0.886 | 19886 | tags=69%, list=36%, signal=108% | |
99 | VIRAL BUDDING VIA HOST ESCRT COMPLEX | 29 | -0.57 | -1.55 | 0.049 | 1.000 | 0.886 | 13663 | tags=72%, list=25%, signal=96% | |
100 | DNA DAMAGE RESPONSE, SIGNAL TRANSDUCTION RESULTING IN TRANSCRIPTION | 36 | -0.46 | -1.55 | 0.013 | 1.000 | 0.886 | 15303 | tags=53%, list=28%, signal=73% | |
101 | 4-HYDROXYPROLINE METABOLIC PROCESS | 17 | -0.50 | -1.55 | 0.039 | 1.000 | 0.888 | 8626 | tags=41%, list=16%, signal=49% | |
102 | REGULATION OF TRANSLATIONAL TERMINATION | 14 | -0.61 | -1.55 | 0.019 | 1.000 | 0.888 | 5758 | tags=50%, list=11%, signal=56% | |
103 | REGULATION OF CELLULAR AMINE METABOLIC PROCESS | 143 | -0.42 | -1.55 | 0.067 | 1.000 | 0.888 | 19835 | tags=62%, list=36%, signal=97% | |
104 | MACROMOLECULAR COMPLEX DISASSEMBLY | 497 | -0.45 | -1.55 | 0.111 | 1.000 | 0.888 | 17321 | tags=64%, list=32%, signal=93% | |
105 | NEGATIVE REGULATION OF ORGANELLE ASSEMBLY | 47 | -0.44 | -1.55 | 0.017 | 1.000 | 0.889 | 25546 | tags=77%, list=47%, signal=144% | |
106 | REGULATION OF RESPIRATORY GASEOUS EXCHANGE | 17 | -0.49 | -1.54 | 0.045 | 1.000 | 0.890 | 11550 | tags=53%, list=21%, signal=67% | |
107 | CALCIUM ION REGULATED EXOCYTOSIS | 47 | -0.44 | -1.54 | 0.023 | 1.000 | 0.890 | 14809 | tags=51%, list=27%, signal=70% | |
108 | CELLULAR RESPIRATION | 277 | -0.45 | -1.54 | 0.082 | 1.000 | 0.891 | 16851 | tags=62%, list=31%, signal=89% | |
109 | HISTONE H4-K5 ACETYLATION | 32 | -0.50 | -1.54 | 0.035 | 1.000 | 0.892 | 13935 | tags=56%, list=25%, signal=75% | |
110 | HISTONE H4-K8 ACETYLATION | 32 | -0.50 | -1.54 | 0.035 | 1.000 | 0.892 | 13935 | tags=56%, list=25%, signal=75% | |
111 | RIBOFLAVIN TRANSPORT | 5 | -0.70 | -1.54 | 0.050 | 1.000 | 0.892 | 6199 | tags=60%, list=11%, signal=68% | |
112 | PROTEIN LOCALIZATION TO MEMBRANE RAFT | 18 | -0.54 | -1.53 | 0.048 | 1.000 | 0.892 | 13287 | tags=61%, list=24%, signal=81% | |
113 | RETINOIC ACID RECEPTOR SIGNALING PATHWAY | 21 | -0.49 | -1.53 | 0.032 | 1.000 | 0.892 | 14123 | tags=52%, list=26%, signal=71% | |
114 | AMINO ACID ACTIVATION | 97 | -0.50 | -1.53 | 0.014 | 1.000 | 0.892 | 18230 | tags=69%, list=33%, signal=103% | |
115 | TRNA AMINOACYLATION | 97 | -0.50 | -1.53 | 0.014 | 1.000 | 0.892 | 18230 | tags=69%, list=33%, signal=103% | |
116 | REGULATION OF PROTEIN UBIQUITINATION INVOLVED IN UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 218 | -0.46 | -1.53 | 0.042 | 1.000 | 0.893 | 18982 | tags=67%, list=35%, signal=101% | |
117 | CELLULAR RESPONSE TO IRON ION | 31 | -0.49 | -1.53 | 0.030 | 1.000 | 0.894 | 7049 | tags=39%, list=13%, signal=44% | |
118 | REGULATION OF PHOSPHOLIPID TRANSPORT | 11 | -0.61 | -1.53 | 0.051 | 1.000 | 0.894 | 12819 | tags=64%, list=23%, signal=83% | |
119 | POSITIVE REGULATION OF PHOSPHOLIPID TRANSPORT | 11 | -0.61 | -1.53 | 0.051 | 1.000 | 0.894 | 12819 | tags=64%, list=23%, signal=83% | |
120 | GLUTATHIONE METABOLIC PROCESS | 61 | -0.44 | -1.53 | 0.035 | 1.000 | 0.895 | 22656 | tags=75%, list=41%, signal=129% | |
121 | REGULATION OF RESPONSE TO ALCOHOL | 11 | -0.58 | -1.52 | 0.073 | 1.000 | 0.898 | 13723 | tags=64%, list=25%, signal=85% | |
122 | POSITIVE REGULATION OF PROTEIN TARGETING TO MEMBRANE | 28 | -0.50 | -1.52 | 0.043 | 1.000 | 0.898 | 9427 | tags=50%, list=17%, signal=60% | |
123 | REGULATION OF LAMELLIPODIUM MORPHOGENESIS | 36 | -0.45 | -1.52 | 0.042 | 1.000 | 0.898 | 14978 | tags=50%, list=27%, signal=69% | |
124 | CELLULAR MODIFIED AMINO ACID METABOLIC PROCESS | 496 | -0.41 | -1.52 | 0.091 | 1.000 | 0.898 | 23206 | tags=68%, list=42%, signal=117% | |
125 | NEGATIVE REGULATION OF GLYCOPROTEIN BIOSYNTHETIC PROCESS | 16 | -0.56 | -1.52 | 0.013 | 1.000 | 0.898 | 20018 | tags=81%, list=37%, signal=128% | |
126 | REGULATION OF SUPEROXIDE ANION GENERATION | 14 | -0.56 | -1.52 | 0.028 | 1.000 | 0.899 | 11512 | tags=57%, list=21%, signal=72% | |
127 | REGULATION OF HISTONE H3-K9 METHYLATION | 15 | -0.54 | -1.52 | 0.022 | 1.000 | 0.899 | 11026 | tags=53%, list=20%, signal=67% | |
128 | ADENYLATE CYCLASE-ACTIVATING DOPAMINE RECEPTOR SIGNALING PATHWAY | 23 | -0.49 | -1.52 | 0.035 | 1.000 | 0.899 | 11449 | tags=43%, list=21%, signal=55% | |
129 | RIBOSOME BIOGENESIS | 179 | -0.45 | -1.52 | 0.044 | 1.000 | 0.899 | 17707 | tags=64%, list=32%, signal=94% | |
130 | TRANSLATIONAL TERMINATION | 377 | -0.48 | -1.52 | 0.130 | 1.000 | 0.899 | 17065 | tags=68%, list=31%, signal=98% | |
131 | RHYTHMIC BEHAVIOR | 20 | -0.52 | -1.52 | 0.021 | 1.000 | 0.900 | 18330 | tags=70%, list=34%, signal=105% | |
132 | CIRCADIAN BEHAVIOR | 20 | -0.52 | -1.52 | 0.021 | 1.000 | 0.900 | 18330 | tags=70%, list=34%, signal=105% | |
133 | FRUCTOSE 1,6-BISPHOSPHATE METABOLIC PROCESS | 15 | -0.56 | -1.51 | 0.063 | 1.000 | 0.900 | 3499 | tags=40%, list=6%, signal=43% | |
134 | HISTONE DEUBIQUITINATION | 54 | -0.49 | -1.51 | 0.013 | 1.000 | 0.900 | 20982 | tags=74%, list=38%, signal=120% | |
135 | REGULATION OF ERAD PATHWAY | 70 | -0.46 | -1.51 | 0.007 | 1.000 | 0.900 | 15185 | tags=57%, list=28%, signal=79% | |
136 | AMYLOID PRECURSOR PROTEIN METABOLIC PROCESS | 26 | -0.48 | -1.51 | 0.061 | 1.000 | 0.900 | 9409 | tags=50%, list=17%, signal=60% | |
137 | TRANSLATION | 753 | -0.44 | -1.51 | 0.088 | 1.000 | 0.900 | 17737 | tags=64%, list=32%, signal=93% | |
138 | PEPTIDYL-PROLINE MODIFICATION | 50 | -0.47 | -1.51 | 0.044 | 1.000 | 0.901 | 19924 | tags=66%, list=36%, signal=104% | |
139 | MULTI-ORGANISM MEMBRANE ORGANIZATION | 43 | -0.53 | -1.51 | 0.046 | 1.000 | 0.901 | 19801 | tags=81%, list=36%, signal=128% | |
140 | PURINE DEOXYRIBONUCLEOTIDE CATABOLIC PROCESS | 18 | -0.53 | -1.51 | 0.040 | 1.000 | 0.903 | 15508 | tags=67%, list=28%, signal=93% | |
141 | PROTEIN K63-LINKED UBIQUITINATION | 81 | -0.43 | -1.50 | 0.052 | 1.000 | 0.903 | 15410 | tags=56%, list=28%, signal=77% | |
142 | CELLULAR PROTEIN COMPLEX DISASSEMBLY | 421 | -0.46 | -1.50 | 0.130 | 1.000 | 0.903 | 17065 | tags=65%, list=31%, signal=94% | |
143 | ENDOSOME TO MELANOSOME TRANSPORT | 19 | -0.51 | -1.50 | 0.030 | 1.000 | 0.903 | 17854 | tags=63%, list=33%, signal=94% | |
144 | ENDOSOME TO PIGMENT GRANULE TRANSPORT | 19 | -0.51 | -1.50 | 0.030 | 1.000 | 0.903 | 17854 | tags=63%, list=33%, signal=94% | |
145 | PIGMENT GRANULE MATURATION | 19 | -0.51 | -1.50 | 0.030 | 1.000 | 0.903 | 17854 | tags=63%, list=33%, signal=94% | |
146 | REGULATION OF MITOCHONDRIAL TRANSLATION | 17 | -0.51 | -1.50 | 0.050 | 1.000 | 0.903 | 10265 | tags=53%, list=19%, signal=65% | |
147 | REGULATION OF SUBSTRATE ADHESION-DEPENDENT CELL SPREADING | 96 | -0.39 | -1.50 | 0.009 | 1.000 | 0.903 | 15032 | tags=48%, list=27%, signal=66% | |
148 | PURINE NUCLEOSIDE MONOPHOSPHATE BIOSYNTHETIC PROCESS | 92 | -0.45 | -1.50 | 0.082 | 1.000 | 0.904 | 18714 | tags=65%, list=34%, signal=99% | |
149 | PURINE RIBONUCLEOSIDE MONOPHOSPHATE BIOSYNTHETIC PROCESS | 92 | -0.45 | -1.50 | 0.082 | 1.000 | 0.904 | 18714 | tags=65%, list=34%, signal=99% | |
150 | ARP2/3 COMPLEX-MEDIATED ACTIN NUCLEATION | 37 | -0.50 | -1.50 | 0.045 | 1.000 | 0.904 | 16272 | tags=59%, list=30%, signal=85% | |
151 | TRANSLATIONAL ELONGATION | 396 | -0.47 | -1.50 | 0.144 | 1.000 | 0.904 | 17027 | tags=67%, list=31%, signal=97% | |
152 | POSITIVE REGULATION OF PROTEIN UBIQUITINATION INVOLVED IN UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 178 | -0.47 | -1.50 | 0.073 | 1.000 | 0.904 | 19472 | tags=71%, list=36%, signal=110% | |
153 | DNA DAMAGE RESPONSE, SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR RESULTING IN TRANSCRIPTION OF P21 CLASS MEDIATOR | 35 | -0.45 | -1.50 | 0.029 | 1.000 | 0.904 | 15303 | tags=51%, list=28%, signal=71% | |
154 | POSITIVE REGULATION OF PEPTIDYL-LYSINE ACETYLATION | 56 | -0.39 | -1.50 | 0.050 | 1.000 | 0.906 | 9583 | tags=39%, list=18%, signal=48% | |
155 | PROTON TRANSPORT | 154 | -0.41 | -1.50 | 0.098 | 1.000 | 0.907 | 19026 | tags=60%, list=35%, signal=91% | |
156 | PEPTIDE BIOSYNTHETIC PROCESS | 789 | -0.43 | -1.50 | 0.084 | 1.000 | 0.907 | 19405 | tags=66%, list=35%, signal=101% | |
157 | RIBONUCLEOSIDE MONOPHOSPHATE BIOSYNTHETIC PROCESS | 101 | -0.45 | -1.49 | 0.091 | 1.000 | 0.908 | 18714 | tags=64%, list=34%, signal=98% | |
158 | COCHLEA DEVELOPMENT | 11 | -0.57 | -1.49 | 0.050 | 1.000 | 0.908 | 14705 | tags=64%, list=27%, signal=87% | |
159 | COCHLEA MORPHOGENESIS | 11 | -0.57 | -1.49 | 0.050 | 1.000 | 0.908 | 14705 | tags=64%, list=27%, signal=87% | |
160 | POSITIVE REGULATION OF ER-ASSOCIATED UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 15 | -0.56 | -1.49 | 0.043 | 1.000 | 0.908 | 13374 | tags=60%, list=24%, signal=79% | |
161 | TRANSLATIONAL INITIATION | 477 | -0.45 | -1.49 | 0.122 | 1.000 | 0.908 | 17027 | tags=65%, list=31%, signal=93% | |
162 | POSITIVE REGULATION OF PROTEIN POLYMERIZATION | 125 | -0.40 | -1.49 | 0.004 | 1.000 | 0.908 | 19703 | tags=54%, list=36%, signal=85% | |
163 | ANAPHASE-PROMOTING COMPLEX-DEPENDENT PROTEASOMAL UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 174 | -0.46 | -1.49 | 0.114 | 1.000 | 0.908 | 20613 | tags=70%, list=38%, signal=112% | |
164 | MULTIVESICULAR BODY ASSEMBLY | 39 | -0.51 | -1.49 | 0.082 | 1.000 | 0.908 | 13663 | tags=64%, list=25%, signal=85% | |
165 | REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 98 | -0.43 | -1.49 | 0.004 | 1.000 | 0.908 | 8091 | tags=42%, list=15%, signal=49% | |
166 | NUCLEOSIDE MONOPHOSPHATE BIOSYNTHETIC PROCESS | 110 | -0.44 | -1.49 | 0.079 | 1.000 | 0.908 | 19013 | tags=65%, list=35%, signal=100% | |
167 | CONTRACTILE ACTIN FILAMENT BUNDLE ASSEMBLY | 33 | -0.45 | -1.49 | 0.056 | 1.000 | 0.908 | 20536 | tags=58%, list=38%, signal=92% | |
168 | STRESS FIBER ASSEMBLY | 33 | -0.45 | -1.49 | 0.056 | 1.000 | 0.908 | 20536 | tags=58%, list=38%, signal=92% | |
169 | NEGATIVE REGULATION OF TOR SIGNALING | 72 | -0.40 | -1.49 | 0.015 | 1.000 | 0.908 | 20305 | tags=57%, list=37%, signal=90% | |
170 | POSITIVE REGULATION OF UBIQUITIN-PROTEIN LIGASE ACTIVITY INVOLVED IN REGULATION OF MITOTIC CELL CYCLE TRANSITION | 160 | -0.47 | -1.49 | 0.088 | 1.000 | 0.908 | 20613 | tags=73%, list=38%, signal=117% | |
171 | POSITIVE REGULATION OF ACTIN FILAMENT POLYMERIZATION | 91 | -0.40 | -1.49 | 0.011 | 1.000 | 0.908 | 19703 | tags=55%, list=36%, signal=86% | |
172 | NIK/NF-KAPPAB SIGNALING | 144 | -0.45 | -1.49 | 0.090 | 1.000 | 0.908 | 20662 | tags=69%, list=38%, signal=111% | |
173 | APOPTOTIC NUCLEAR CHANGES | 41 | -0.49 | -1.49 | 0.033 | 1.000 | 0.908 | 17224 | tags=66%, list=32%, signal=96% | |
174 | NEGATIVE REGULATION OF AUTOPHAGOSOME ASSEMBLY | 16 | -0.56 | -1.49 | 0.034 | 1.000 | 0.908 | 14677 | tags=75%, list=27%, signal=102% | |
175 | PEPTIDE METABOLIC PROCESS | 916 | -0.41 | -1.49 | 0.088 | 1.000 | 0.908 | 17737 | tags=59%, list=32%, signal=86% | |
176 | GLUTAMINE TRANSPORT | 11 | -0.60 | -1.49 | 0.059 | 1.000 | 0.908 | 15639 | tags=73%, list=29%, signal=102% | |
177 | NUCLEOBASE-CONTAINING SMALL MOLECULE INTERCONVERSION | 53 | -0.47 | -1.49 | 0.016 | 1.000 | 0.908 | 19622 | tags=68%, list=36%, signal=106% | |
178 | POSITIVE REGULATION OF INTERLEUKIN-6 SECRETION | 17 | -0.52 | -1.48 | 0.039 | 1.000 | 0.909 | 12614 | tags=59%, list=23%, signal=76% | |
179 | INTRACELLULAR STEROL TRANSPORT | 11 | -0.59 | -1.48 | 0.045 | 1.000 | 0.909 | 6711 | tags=55%, list=12%, signal=62% | |
180 | INTRACELLULAR CHOLESTEROL TRANSPORT | 11 | -0.59 | -1.48 | 0.045 | 1.000 | 0.909 | 6711 | tags=55%, list=12%, signal=62% | |
181 | HYDROGEN TRANSPORT | 155 | -0.40 | -1.48 | 0.098 | 1.000 | 0.911 | 19026 | tags=59%, list=35%, signal=91% | |
182 | VIRAL GENOME REPLICATION | 26 | -0.46 | -1.48 | 0.028 | 1.000 | 0.912 | 16095 | tags=62%, list=29%, signal=87% | |
183 | ANTIGEN PROCESSING AND PRESENTATION OF EXOGENOUS PEPTIDE ANTIGEN VIA MHC CLASS I, TAP-DEPENDENT | 156 | -0.45 | -1.48 | 0.056 | 1.000 | 0.912 | 19835 | tags=69%, list=36%, signal=108% | |
184 | CHOLINE TRANSPORT | 14 | -0.55 | -1.48 | 0.042 | 1.000 | 0.912 | 1200 | tags=36%, list=2%, signal=37% | |
185 | CENTRAL NERVOUS SYSTEM MYELINATION | 18 | -0.53 | -1.48 | 0.057 | 1.000 | 0.912 | 18817 | tags=72%, list=34%, signal=110% | |
186 | AXON ENSHEATHMENT IN CENTRAL NERVOUS SYSTEM | 18 | -0.53 | -1.48 | 0.057 | 1.000 | 0.912 | 18817 | tags=72%, list=34%, signal=110% | |
187 | HYDROGEN ION TRANSMEMBRANE TRANSPORT | 116 | -0.44 | -1.48 | 0.128 | 1.000 | 0.912 | 18490 | tags=62%, list=34%, signal=94% | |
188 | AMIDE BIOSYNTHETIC PROCESS | 848 | -0.42 | -1.48 | 0.090 | 1.000 | 0.912 | 19405 | tags=63%, list=35%, signal=97% | |
189 | REGULATION OF SUPEROXIDE METABOLIC PROCESS | 30 | -0.48 | -1.48 | 0.032 | 1.000 | 0.913 | 11571 | tags=50%, list=21%, signal=63% | |
190 | MITOCHONDRIAL TRANSPORT | 335 | -0.41 | -1.48 | 0.059 | 1.000 | 0.913 | 21021 | tags=64%, list=38%, signal=104% | |
191 | CHAPERONE-MEDIATED PROTEIN TRANSPORT | 16 | -0.53 | -1.47 | 0.091 | 1.000 | 0.913 | 13722 | tags=63%, list=25%, signal=83% | |
192 | POSITIVE REGULATION OF IMMUNOGLOBULIN PRODUCTION | 29 | -0.49 | -1.47 | 0.092 | 1.000 | 0.913 | 5072 | tags=38%, list=9%, signal=42% | |
193 | ESTABLISHMENT OR MAINTENANCE OF MONOPOLAR CELL POLARITY | 10 | -0.57 | -1.47 | 0.055 | 1.000 | 0.913 | 21116 | tags=80%, list=39%, signal=130% | |
194 | GLUTATHIONE DERIVATIVE METABOLIC PROCESS | 58 | -0.46 | -1.47 | 0.055 | 1.000 | 0.913 | 23642 | tags=81%, list=43%, signal=143% | |
195 | GLUTATHIONE DERIVATIVE BIOSYNTHETIC PROCESS | 58 | -0.46 | -1.47 | 0.055 | 1.000 | 0.913 | 23642 | tags=81%, list=43%, signal=143% | |
196 | REGULATION OF BETA-AMYLOID CLEARANCE | 15 | -0.57 | -1.47 | 0.042 | 1.000 | 0.913 | 13546 | tags=67%, list=25%, signal=89% | |
197 | REGULATION OF MITOCHONDRIAL MEMBRANE PERMEABILITY | 129 | -0.40 | -1.47 | 0.002 | 1.000 | 0.913 | 8091 | tags=39%, list=15%, signal=45% | |
198 | RIBONUCLEOSIDE TRIPHOSPHATE METABOLIC PROCESS | 190 | -0.40 | -1.47 | 0.073 | 1.000 | 0.913 | 21242 | tags=63%, list=39%, signal=102% | |
199 | POSITIVE REGULATION OF PROTEIN ACETYLATION | 66 | -0.38 | -1.47 | 0.047 | 1.000 | 0.913 | 10067 | tags=39%, list=18%, signal=48% | |
200 | REGULATION OF DEOXYRIBONUCLEASE ACTIVITY | 14 | -0.57 | -1.47 | 0.047 | 1.000 | 0.913 | 16702 | tags=79%, list=31%, signal=113% | |
201 | NUCLEOBASE-CONTAINING SMALL MOLECULE CATABOLIC PROCESS | 12 | -0.59 | -1.47 | 0.049 | 1.000 | 0.913 | 11907 | tags=67%, list=22%, signal=85% | |
202 | DNA DAMAGE RESPONSE, SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR RESULTING IN CELL CYCLE ARREST | 148 | -0.42 | -1.47 | 0.084 | 1.000 | 0.914 | 19472 | tags=64%, list=36%, signal=99% | |
203 | MITOTIC G1 DNA DAMAGE CHECKPOINT | 162 | -0.42 | -1.47 | 0.084 | 1.000 | 0.914 | 21273 | tags=68%, list=39%, signal=111% | |
204 | MITOTIC G1/S TRANSITION CHECKPOINT | 165 | -0.42 | -1.47 | 0.080 | 1.000 | 0.914 | 21273 | tags=68%, list=39%, signal=111% | |
205 | PURINE RIBONUCLEOSIDE TRIPHOSPHATE METABOLIC PROCESS | 189 | -0.40 | -1.47 | 0.073 | 1.000 | 0.915 | 21242 | tags=62%, list=39%, signal=102% | |
206 | NUCLEOSIDE TRIPHOSPHATE METABOLIC PROCESS | 224 | -0.39 | -1.47 | 0.064 | 1.000 | 0.916 | 20756 | tags=60%, list=38%, signal=96% | |
207 | NEGATIVE REGULATION OF HISTONE H3-K9 METHYLATION | 7 | -0.61 | -1.47 | 0.039 | 1.000 | 0.916 | 7264 | tags=57%, list=13%, signal=66% | |
208 | NEGATIVE REGULATION OF GLYCOPROTEIN METABOLIC PROCESS | 20 | -0.52 | -1.47 | 0.019 | 1.000 | 0.916 | 20018 | tags=75%, list=37%, signal=118% | |
209 | POLYAMINE METABOLIC PROCESS | 159 | -0.41 | -1.47 | 0.098 | 1.000 | 0.917 | 19835 | tags=61%, list=36%, signal=95% | |
210 | POSITIVE REGULATION OF UBIQUITIN-PROTEIN TRANSFERASE ACTIVITY | 193 | -0.45 | -1.46 | 0.093 | 1.000 | 0.917 | 20785 | tags=70%, list=38%, signal=112% | |
211 | PHOSPHATIDYLGLYCEROL METABOLIC PROCESS | 73 | -0.40 | -1.46 | 0.038 | 1.000 | 0.917 | 24207 | tags=68%, list=44%, signal=123% | |
212 | GLUCONEOGENESIS | 74 | -0.43 | -1.46 | 0.116 | 1.000 | 0.917 | 10537 | tags=45%, list=19%, signal=55% | |
213 | NEGATIVE REGULATION OF PROTEIN TARGETING TO MEMBRANE | 9 | -0.61 | -1.46 | 0.056 | 1.000 | 0.917 | 13561 | tags=67%, list=25%, signal=89% | |
214 | VIRAL BUDDING | 36 | -0.53 | -1.46 | 0.082 | 1.000 | 0.918 | 19801 | tags=81%, list=36%, signal=126% | |
215 | MULTI-ORGANISM ORGANELLE ORGANIZATION | 36 | -0.53 | -1.46 | 0.082 | 1.000 | 0.918 | 19801 | tags=81%, list=36%, signal=126% | |
216 | MULTI-ORGANISM MEMBRANE BUDDING | 36 | -0.53 | -1.46 | 0.082 | 1.000 | 0.918 | 19801 | tags=81%, list=36%, signal=126% | |
217 | SIGNAL TRANSDUCTION INVOLVED IN MITOTIC G1 DNA DAMAGE CHECKPOINT | 151 | -0.42 | -1.46 | 0.086 | 1.000 | 0.918 | 19472 | tags=64%, list=36%, signal=99% | |
218 | INTRACELLULAR SIGNAL TRANSDUCTION INVOLVED IN G1 DNA DAMAGE CHECKPOINT | 151 | -0.42 | -1.46 | 0.086 | 1.000 | 0.918 | 19472 | tags=64%, list=36%, signal=99% | |
219 | POSITIVE REGULATION OF CELL CYCLE ARREST | 193 | -0.40 | -1.46 | 0.068 | 1.000 | 0.918 | 25186 | tags=71%, list=46%, signal=131% | |
220 | MULTI-ORGANISM METABOLIC PROCESS | 291 | -0.46 | -1.46 | 0.154 | 1.000 | 0.918 | 16840 | tags=65%, list=31%, signal=93% | |
221 | PLASMA MEMBRANE TO ENDOSOME TRANSPORT | 14 | -0.58 | -1.46 | 0.059 | 1.000 | 0.918 | 15269 | tags=79%, list=28%, signal=109% | |
222 | PURINE NUCLEOSIDE TRIPHOSPHATE METABOLIC PROCESS | 201 | -0.39 | -1.46 | 0.071 | 1.000 | 0.918 | 21242 | tags=62%, list=39%, signal=101% | |
223 | ATP METABOLIC PROCESS | 177 | -0.40 | -1.46 | 0.106 | 1.000 | 0.918 | 21242 | tags=62%, list=39%, signal=100% | |
224 | POSITIVE REGULATION OF LAMELLIPODIUM MORPHOGENESIS | 33 | -0.44 | -1.46 | 0.084 | 1.000 | 0.918 | 14978 | tags=48%, list=27%, signal=67% | |
225 | ESTABLISHMENT OF EPITHELIAL CELL POLARITY | 22 | -0.50 | -1.46 | 0.053 | 1.000 | 0.918 | 9068 | tags=45%, list=17%, signal=54% | |
226 | L-ALANINE TRANSPORT | 8 | -0.60 | -1.46 | 0.067 | 1.000 | 0.920 | 20980 | tags=88%, list=38%, signal=142% | |
227 | REGULATION OF CELLULAR RESPIRATION | 21 | -0.50 | -1.46 | 0.069 | 1.000 | 0.920 | 14129 | tags=57%, list=26%, signal=77% | |
228 | MATURATION OF SSU-RRNA | 12 | -0.56 | -1.46 | 0.097 | 1.000 | 0.921 | 22380 | tags=83%, list=41%, signal=141% | |
229 | NEGATIVE REGULATION OF PHOSPHATIDYLINOSITOL 3-KINASE SIGNALING | 22 | -0.51 | -1.46 | 0.050 | 1.000 | 0.922 | 18246 | tags=68%, list=33%, signal=102% | |
230 | POSITIVE REGULATION OF HISTONE H4 ACETYLATION | 18 | -0.53 | -1.46 | 0.086 | 1.000 | 0.922 | 15303 | tags=61%, list=28%, signal=85% | |
231 | NUCLEAR-TRANSCRIBED MRNA CATABOLIC PROCESS, NONSENSE-MEDIATED DECAY | 277 | -0.46 | -1.46 | 0.169 | 1.000 | 0.922 | 23210 | tags=78%, list=42%, signal=134% | |
232 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO MITOCHONDRIAL MEMBRANE | 22 | -0.51 | -1.46 | 0.082 | 1.000 | 0.922 | 20106 | tags=73%, list=37%, signal=115% | |
233 | INTRINSIC APOPTOTIC SIGNALING PATHWAY BY P53 CLASS MEDIATOR | 87 | -0.42 | -1.45 | 0.028 | 1.000 | 0.922 | 23895 | tags=71%, list=44%, signal=126% | |
234 | VIRAL GENE EXPRESSION | 289 | -0.46 | -1.45 | 0.154 | 1.000 | 0.922 | 16840 | tags=65%, list=31%, signal=93% | |
235 | G1 DNA DAMAGE CHECKPOINT | 168 | -0.42 | -1.45 | 0.089 | 1.000 | 0.922 | 21273 | tags=68%, list=39%, signal=111% | |
236 | SINGLE-ORGANISM MEMBRANE FUSION | 122 | -0.43 | -1.45 | 0.074 | 1.000 | 0.922 | 13864 | tags=51%, list=25%, signal=68% | |
237 | NEGATIVE REGULATION OF VIRAL RELEASE FROM HOST CELL | 40 | -0.45 | -1.45 | 0.044 | 1.000 | 0.922 | 22427 | tags=68%, list=41%, signal=114% | |
238 | HEME METABOLIC PROCESS | 48 | -0.46 | -1.45 | 0.099 | 1.000 | 0.923 | 20140 | tags=69%, list=37%, signal=109% | |
239 | FATTY ACID OXIDATION | 100 | -0.43 | -1.45 | 0.092 | 1.000 | 0.923 | 19886 | tags=64%, list=36%, signal=100% | |
240 | ANTIGEN PROCESSING AND PRESENTATION OF EXOGENOUS PEPTIDE ANTIGEN VIA MHC CLASS I | 165 | -0.44 | -1.45 | 0.074 | 1.000 | 0.923 | 19835 | tags=68%, list=36%, signal=106% | |
241 | REGULATION OF CELL CYCLE ARREST | 231 | -0.38 | -1.45 | 0.069 | 1.000 | 0.924 | 25311 | tags=68%, list=46%, signal=126% | |
242 | RESPONSE TO EXOGENOUS DSRNA | 29 | -0.47 | -1.45 | 0.043 | 1.000 | 0.924 | 15412 | tags=59%, list=28%, signal=82% | |
243 | REGULATION OF ER-ASSOCIATED UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 22 | -0.51 | -1.45 | 0.082 | 1.000 | 0.924 | 14846 | tags=59%, list=27%, signal=81% | |
244 | NUCLEOSIDE MONOPHOSPHATE METABOLIC PROCESS | 265 | -0.39 | -1.45 | 0.088 | 1.000 | 0.924 | 21242 | tags=61%, list=39%, signal=99% | |
245 | PROTEIN EXPORT FROM NUCLEUS | 53 | -0.44 | -1.45 | 0.028 | 0.997 | 0.924 | 18498 | tags=60%, list=34%, signal=91% | |
246 | POSITIVE REGULATION OF LIGASE ACTIVITY | 198 | -0.45 | -1.45 | 0.098 | 0.998 | 0.924 | 20785 | tags=69%, list=38%, signal=111% | |
247 | MULTIVESICULAR BODY ORGANIZATION | 44 | -0.49 | -1.45 | 0.079 | 0.996 | 0.925 | 13663 | tags=61%, list=25%, signal=82% | |
248 | PLATELET FORMATION | 22 | -0.45 | -1.45 | 0.100 | 0.993 | 0.925 | 10833 | tags=41%, list=20%, signal=51% | |
249 | PLATELET MORPHOGENESIS | 22 | -0.45 | -1.45 | 0.100 | 0.989 | 0.925 | 10833 | tags=41%, list=20%, signal=51% | |
250 | MISFOLDED OR INCOMPLETELY SYNTHESIZED PROTEIN CATABOLIC PROCESS | 45 | -0.45 | -1.45 | 0.028 | 0.991 | 0.925 | 15267 | tags=58%, list=28%, signal=80% | |
251 | ORGANELLE FUSION | 118 | -0.43 | -1.45 | 0.077 | 0.990 | 0.925 | 13864 | tags=52%, list=25%, signal=69% | |
252 | MITOCHONDRIAL FRAGMENTATION INVOLVED IN APOPTOTIC PROCESS | 18 | -0.53 | -1.45 | 0.052 | 0.989 | 0.925 | 21395 | tags=78%, list=39%, signal=128% | |
253 | SIGNAL TRANSDUCTION INVOLVED IN MITOTIC CELL CYCLE CHECKPOINT | 152 | -0.42 | -1.45 | 0.089 | 0.989 | 0.925 | 19472 | tags=64%, list=36%, signal=99% | |
254 | SIGNAL TRANSDUCTION INVOLVED IN MITOTIC DNA DAMAGE CHECKPOINT | 152 | -0.42 | -1.45 | 0.089 | 0.985 | 0.925 | 19472 | tags=64%, list=36%, signal=99% | |
255 | SIGNAL TRANSDUCTION INVOLVED IN MITOTIC DNA INTEGRITY CHECKPOINT | 152 | -0.42 | -1.45 | 0.089 | 0.981 | 0.925 | 19472 | tags=64%, list=36%, signal=99% | |
256 | REGULATION OF MEMBRANE PERMEABILITY | 138 | -0.39 | -1.45 | 0.000 | 0.978 | 0.925 | 8091 | tags=38%, list=15%, signal=45% | |
257 | NEGATIVE REGULATION OF PROTEIN UBIQUITINATION INVOLVED IN UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 31 | -0.47 | -1.44 | 0.051 | 0.986 | 0.927 | 10311 | tags=45%, list=19%, signal=56% | |
258 | CELL SEPARATION AFTER CYTOKINESIS | 26 | -0.54 | -1.44 | 0.088 | 0.983 | 0.927 | 13663 | tags=69%, list=25%, signal=92% | |
259 | POSITIVE REGULATION OF RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 57 | -0.48 | -1.44 | 0.040 | 0.982 | 0.927 | 22081 | tags=79%, list=40%, signal=132% | |
260 | REGULATION OF ENDODEOXYRIBONUCLEASE ACTIVITY | 13 | -0.56 | -1.44 | 0.064 | 0.985 | 0.927 | 16702 | tags=77%, list=31%, signal=111% | |
261 | GLUCOSE CATABOLIC PROCESS | 67 | -0.41 | -1.44 | 0.120 | 0.984 | 0.927 | 9676 | tags=37%, list=18%, signal=45% | |
262 | NEGATIVE REGULATION OF BETA-AMYLOID FORMATION | 14 | -0.52 | -1.44 | 0.086 | 0.994 | 0.928 | 13546 | tags=57%, list=25%, signal=76% | |
263 | PROTEIN POLYUBIQUITINATION | 445 | -0.41 | -1.44 | 0.055 | 0.991 | 0.928 | 21267 | tags=64%, list=39%, signal=105% | |
264 | NEGATIVE REGULATION OF NITRIC-OXIDE SYNTHASE ACTIVITY | 8 | -0.56 | -1.44 | 0.082 | 1.000 | 0.930 | 11362 | tags=50%, list=21%, signal=63% | |
265 | SPHINGOID BIOSYNTHETIC PROCESS | 13 | -0.52 | -1.44 | 0.085 | 0.999 | 0.931 | 11350 | tags=54%, list=21%, signal=68% | |
266 | MAINTENANCE OF PROTEIN LOCALIZATION IN ENDOPLASMIC RETICULUM | 15 | -0.48 | -1.44 | 0.064 | 0.997 | 0.931 | 18436 | tags=60%, list=34%, signal=90% | |
267 | UV PROTECTION | 18 | -0.50 | -1.44 | 0.099 | 0.996 | 0.931 | 23576 | tags=89%, list=43%, signal=156% | |
268 | SPLICEOSOMAL SNRNP ASSEMBLY | 68 | -0.44 | -1.44 | 0.108 | 0.997 | 0.931 | 20057 | tags=68%, list=37%, signal=107% | |
269 | MONOSACCHARIDE BIOSYNTHETIC PROCESS | 85 | -0.41 | -1.43 | 0.132 | 1.000 | 0.934 | 22787 | tags=67%, list=42%, signal=115% | |
270 | RETROGRADE VESICLE-MEDIATED TRANSPORT, GOLGI TO ER | 52 | -0.45 | -1.43 | 0.072 | 0.998 | 0.934 | 24251 | tags=75%, list=44%, signal=135% | |
271 | POSITIVE REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 85 | -0.42 | -1.43 | 0.016 | 0.995 | 0.934 | 8035 | tags=41%, list=15%, signal=48% | |
272 | CELLULAR RESPONSE TO TOPOLOGICALLY INCORRECT PROTEIN | 262 | -0.39 | -1.43 | 0.044 | 1.000 | 0.934 | 17858 | tags=56%, list=33%, signal=82% | |
273 | MULTICELLULAR ORGANISMAL MOVEMENT | 32 | -0.47 | -1.43 | 0.134 | 1.000 | 0.935 | 14748 | tags=47%, list=27%, signal=64% | |
274 | MUSCULOSKELETAL MOVEMENT | 32 | -0.47 | -1.43 | 0.134 | 1.000 | 0.935 | 14748 | tags=47%, list=27%, signal=64% | |
275 | VIRAL TRANSCRIPTION | 270 | -0.46 | -1.43 | 0.168 | 1.000 | 0.935 | 17573 | tags=66%, list=32%, signal=96% | |
276 | RIBOSOMAL LARGE SUBUNIT BIOGENESIS | 41 | -0.44 | -1.43 | 0.093 | 0.997 | 0.936 | 22750 | tags=73%, list=42%, signal=125% | |
277 | DNA CATABOLIC PROCESS, ENDONUCLEOLYTIC | 34 | -0.48 | -1.43 | 0.069 | 0.994 | 0.936 | 18611 | tags=68%, list=34%, signal=102% | |
278 | RESPONSE TO TOPOLOGICALLY INCORRECT PROTEIN | 305 | -0.38 | -1.43 | 0.040 | 0.998 | 0.936 | 17858 | tags=55%, list=33%, signal=81% | |
279 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO HYPOXIA | 86 | -0.40 | -1.43 | 0.063 | 0.994 | 0.936 | 23082 | tags=64%, list=42%, signal=111% | |
280 | LIPID OXIDATION | 101 | -0.42 | -1.43 | 0.103 | 1.000 | 0.939 | 19886 | tags=63%, list=36%, signal=99% | |
281 | NADH METABOLIC PROCESS | 65 | -0.40 | -1.43 | 0.126 | 1.000 | 0.939 | 9676 | tags=38%, list=18%, signal=47% | |
282 | SIGNAL TRANSDUCTION INVOLVED IN CELL CYCLE CHECKPOINT | 159 | -0.41 | -1.43 | 0.100 | 1.000 | 0.939 | 19472 | tags=62%, list=36%, signal=95% | |
283 | COPPER ION HOMEOSTASIS | 21 | -0.51 | -1.43 | 0.088 | 1.000 | 0.939 | 18982 | tags=76%, list=35%, signal=117% | |
284 | NEGATIVE REGULATION OF UBIQUITIN-PROTEIN LIGASE ACTIVITY INVOLVED IN MITOTIC CELL CYCLE | 180 | -0.43 | -1.42 | 0.092 | 1.000 | 0.941 | 18818 | tags=63%, list=34%, signal=96% | |
285 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO MEMBRANE | 592 | -0.39 | -1.42 | 0.115 | 1.000 | 0.941 | 22652 | tags=65%, list=41%, signal=110% | |
286 | SIGNAL TRANSDUCTION INVOLVED IN DNA INTEGRITY CHECKPOINT | 156 | -0.41 | -1.42 | 0.103 | 1.000 | 0.941 | 19472 | tags=63%, list=36%, signal=97% | |
287 | SIGNAL TRANSDUCTION INVOLVED IN DNA DAMAGE CHECKPOINT | 156 | -0.41 | -1.42 | 0.103 | 1.000 | 0.941 | 19472 | tags=63%, list=36%, signal=97% | |
288 | ENDOSOMAL VESICLE FUSION | 16 | -0.50 | -1.42 | 0.059 | 1.000 | 0.941 | 9294 | tags=44%, list=17%, signal=53% | |
289 | REGULATION OF MACROAUTOPHAGY | 225 | -0.39 | -1.42 | 0.002 | 1.000 | 0.941 | 18627 | tags=56%, list=34%, signal=85% | |
290 | HEXOSE CATABOLIC PROCESS | 81 | -0.40 | -1.42 | 0.115 | 1.000 | 0.941 | 10089 | tags=38%, list=18%, signal=47% | |
291 | REGULATION OF ENDOPLASMIC RETICULUM UNFOLDED PROTEIN RESPONSE | 51 | -0.43 | -1.42 | 0.035 | 0.999 | 0.941 | 20833 | tags=69%, list=38%, signal=111% | |
292 | NUCLEAR-TRANSCRIBED MRNA CATABOLIC PROCESS | 437 | -0.43 | -1.42 | 0.102 | 0.997 | 0.941 | 23417 | tags=73%, list=43%, signal=127% | |
293 | PIGMENT ACCUMULATION | 23 | -0.45 | -1.42 | 0.058 | 0.996 | 0.941 | 17854 | tags=57%, list=33%, signal=84% | |
294 | CELLULAR PIGMENT ACCUMULATION | 23 | -0.45 | -1.42 | 0.058 | 0.993 | 0.941 | 17854 | tags=57%, list=33%, signal=84% | |
295 | CARBOHYDRATE BIOSYNTHETIC PROCESS | 158 | -0.38 | -1.42 | 0.125 | 0.990 | 0.941 | 22067 | tags=60%, list=40%, signal=101% | |
296 | RRNA TRANSCRIPTION | 19 | -0.45 | -1.42 | 0.070 | 0.989 | 0.941 | 8657 | tags=42%, list=16%, signal=50% | |
297 | CARBOHYDRATE CATABOLIC PROCESS | 150 | -0.37 | -1.42 | 0.075 | 0.988 | 0.941 | 19443 | tags=53%, list=36%, signal=82% | |
298 | POSITIVE REGULATION OF CANONICAL WNT SIGNALING PATHWAY | 256 | -0.38 | -1.42 | 0.071 | 0.987 | 0.941 | 19835 | tags=55%, list=36%, signal=87% | |
299 | POSITIVE REGULATION OF T CELL APOPTOTIC PROCESS | 14 | -0.52 | -1.42 | 0.113 | 0.984 | 0.941 | 6805 | tags=43%, list=12%, signal=49% | |
300 | PROTEIN K11-LINKED UBIQUITINATION | 80 | -0.45 | -1.42 | 0.096 | 0.982 | 0.941 | 17763 | tags=65%, list=32%, signal=96% | |
301 | N-TERMINAL PROTEIN AMINO ACID MODIFICATION | 54 | -0.41 | -1.42 | 0.070 | 0.979 | 0.942 | 15728 | tags=52%, list=29%, signal=73% | |
302 | PHOSPHATIDYLSERINE METABOLIC PROCESS | 38 | -0.42 | -1.42 | 0.075 | 0.980 | 0.942 | 23706 | tags=68%, list=43%, signal=121% | |
303 | VESICLE FUSION | 51 | -0.43 | -1.42 | 0.078 | 0.978 | 0.942 | 19971 | tags=61%, list=37%, signal=96% | |
304 | REGULATION OF MRNA POLYADENYLATION | 16 | -0.48 | -1.42 | 0.093 | 0.975 | 0.942 | 19323 | tags=63%, list=35%, signal=97% | |
305 | RIBONUCLEOSIDE MONOPHOSPHATE METABOLIC PROCESS | 253 | -0.38 | -1.42 | 0.092 | 0.972 | 0.942 | 21242 | tags=60%, list=39%, signal=98% | |
306 | PURINE NUCLEOSIDE MONOPHOSPHATE METABOLIC PROCESS | 244 | -0.38 | -1.42 | 0.091 | 0.970 | 0.942 | 21242 | tags=60%, list=39%, signal=98% | |
307 | PURINE RIBONUCLEOSIDE MONOPHOSPHATE METABOLIC PROCESS | 244 | -0.38 | -1.42 | 0.091 | 0.967 | 0.942 | 21242 | tags=60%, list=39%, signal=98% | |
308 | REGULATION OF MICROVILLUS ORGANIZATION | 14 | -0.54 | -1.42 | 0.094 | 0.969 | 0.942 | 18813 | tags=71%, list=34%, signal=109% | |
309 | REGULATION OF MICROVILLUS ASSEMBLY | 14 | -0.54 | -1.42 | 0.094 | 0.966 | 0.942 | 18813 | tags=71%, list=34%, signal=109% | |
310 | ALANINE TRANSPORT | 10 | -0.53 | -1.42 | 0.109 | 0.968 | 0.943 | 22668 | tags=80%, list=41%, signal=137% | |
311 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO MITOCHONDRION | 263 | -0.36 | -1.42 | 0.018 | 0.969 | 0.943 | 16162 | tags=47%, list=30%, signal=67% | |
312 | RESPONSE TO THYROID HORMONE | 30 | -0.44 | -1.42 | 0.054 | 0.973 | 0.943 | 16096 | tags=53%, list=29%, signal=76% | |
313 | PROTEIN LOCALIZATION TO ENDOPLASMIC RETICULUM | 317 | -0.44 | -1.41 | 0.170 | 0.975 | 0.943 | 17625 | tags=65%, list=32%, signal=95% | |
314 | MRNA CATABOLIC PROCESS | 455 | -0.42 | -1.41 | 0.100 | 0.974 | 0.943 | 23310 | tags=73%, list=43%, signal=125% | |
315 | MONOCARBOXYLIC ACID CATABOLIC PROCESS | 131 | -0.38 | -1.41 | 0.106 | 0.975 | 0.944 | 20089 | tags=57%, list=37%, signal=90% | |
316 | DEOXYRIBONUCLEOTIDE METABOLIC PROCESS | 47 | -0.42 | -1.41 | 0.069 | 0.973 | 0.944 | 17898 | tags=57%, list=33%, signal=85% | |
317 | GLYCOLYTIC PROCESS THROUGH FRUCTOSE-6-PHOSPHATE | 63 | -0.40 | -1.41 | 0.135 | 0.970 | 0.944 | 9676 | tags=38%, list=18%, signal=46% | |
318 | NADH REGENERATION | 63 | -0.40 | -1.41 | 0.135 | 0.967 | 0.944 | 9676 | tags=38%, list=18%, signal=46% | |
319 | GLYCOLYTIC PROCESS THROUGH GLUCOSE-6-PHOSPHATE | 63 | -0.40 | -1.41 | 0.135 | 0.964 | 0.944 | 9676 | tags=38%, list=18%, signal=46% | |
320 | CANONICAL GLYCOLYSIS | 63 | -0.40 | -1.41 | 0.135 | 0.961 | 0.944 | 9676 | tags=38%, list=18%, signal=46% | |
321 | GLUCOSE CATABOLIC PROCESS TO PYRUVATE | 63 | -0.40 | -1.41 | 0.135 | 0.958 | 0.944 | 9676 | tags=38%, list=18%, signal=46% | |
322 | REGULATION OF HISTONE H4 ACETYLATION | 26 | -0.47 | -1.41 | 0.086 | 0.957 | 0.944 | 15303 | tags=58%, list=28%, signal=80% | |
323 | REGULATION OF UBIQUITIN-PROTEIN LIGASE ACTIVITY INVOLVED IN MITOTIC CELL CYCLE | 213 | -0.43 | -1.41 | 0.091 | 0.955 | 0.944 | 18818 | tags=62%, list=34%, signal=94% | |
324 | MITOCHONDRION MORPHOGENESIS | 22 | -0.49 | -1.41 | 0.061 | 0.955 | 0.945 | 22599 | tags=73%, list=41%, signal=124% | |
325 | POSITIVE REGULATION OF INTERLEUKIN-13 PRODUCTION | 21 | -0.49 | -1.41 | 0.101 | 0.954 | 0.946 | 14287 | tags=48%, list=26%, signal=64% | |
326 | PROTEIN TARGETING TO MEMBRANE | 374 | -0.42 | -1.41 | 0.172 | 0.951 | 0.946 | 17642 | tags=60%, list=32%, signal=88% | |
327 | VIRAL LIFE CYCLE | 524 | -0.41 | -1.41 | 0.140 | 0.948 | 0.946 | 16733 | tags=58%, list=31%, signal=83% | |
328 | MITOTIC NUCLEAR ENVELOPE REASSEMBLY | 23 | -0.49 | -1.41 | 0.088 | 0.947 | 0.946 | 22528 | tags=78%, list=41%, signal=133% | |
329 | NUCLEAR ENVELOPE REASSEMBLY | 23 | -0.49 | -1.41 | 0.088 | 0.944 | 0.946 | 22528 | tags=78%, list=41%, signal=133% | |
330 | ENDOPLASMIC RETICULUM UNFOLDED PROTEIN RESPONSE | 224 | -0.40 | -1.41 | 0.062 | 0.942 | 0.947 | 21062 | tags=62%, list=39%, signal=101% | |
331 | UBIQUINONE METABOLIC PROCESS | 20 | -0.52 | -1.41 | 0.057 | 0.946 | 0.947 | 13145 | tags=65%, list=24%, signal=86% | |
332 | UBIQUINONE BIOSYNTHETIC PROCESS | 20 | -0.52 | -1.41 | 0.057 | 0.943 | 0.947 | 13145 | tags=65%, list=24%, signal=86% | |
333 | QUINONE BIOSYNTHETIC PROCESS | 20 | -0.52 | -1.41 | 0.057 | 0.940 | 0.947 | 13145 | tags=65%, list=24%, signal=86% | |
334 | FATTY ACID BETA-OXIDATION USING ACYL-COA OXIDASE | 28 | -0.45 | -1.41 | 0.098 | 0.938 | 0.947 | 19710 | tags=64%, list=36%, signal=100% | |
335 | SINGLE-ORGANISM CARBOHYDRATE CATABOLIC PROCESS | 141 | -0.37 | -1.41 | 0.089 | 0.936 | 0.947 | 19443 | tags=52%, list=36%, signal=80% | |
336 | EXIT FROM MITOSIS | 15 | -0.54 | -1.41 | 0.095 | 0.936 | 0.947 | 21284 | tags=87%, list=39%, signal=142% | |
337 | LOCOMOTOR RHYTHM | 18 | -0.49 | -1.41 | 0.080 | 0.935 | 0.947 | 18330 | tags=67%, list=34%, signal=100% | |
338 | NEGATIVE REGULATION OF CELL CYCLE G1/S PHASE TRANSITION | 225 | -0.40 | -1.41 | 0.080 | 0.933 | 0.947 | 21273 | tags=64%, list=39%, signal=104% | |
339 | REGULATION OF PROTEIN DEUBIQUITINATION | 17 | -0.50 | -1.41 | 0.093 | 0.933 | 0.948 | 14061 | tags=59%, list=26%, signal=79% | |
340 | REGULATION OF RECEPTOR BINDING | 49 | -0.41 | -1.41 | 0.034 | 0.932 | 0.948 | 13128 | tags=41%, list=24%, signal=54% | |
341 | NEGATIVE REGULATION OF LIGASE ACTIVITY | 192 | -0.42 | -1.41 | 0.099 | 0.931 | 0.948 | 18818 | tags=62%, list=34%, signal=94% | |
342 | NEGATIVE REGULATION OF UBIQUITIN-PROTEIN TRANSFERASE ACTIVITY | 192 | -0.42 | -1.41 | 0.099 | 0.928 | 0.948 | 18818 | tags=62%, list=34%, signal=94% | |
343 | APOPTOTIC CHROMOSOME CONDENSATION | 7 | -0.58 | -1.41 | 0.079 | 0.925 | 0.948 | 13423 | tags=57%, list=25%, signal=76% | |
344 | PORPHYRIN-CONTAINING COMPOUND METABOLIC PROCESS | 50 | -0.44 | -1.41 | 0.124 | 0.923 | 0.948 | 20140 | tags=66%, list=37%, signal=104% | |
345 | SRP-DEPENDENT COTRANSLATIONAL PROTEIN TARGETING TO MEMBRANE | 259 | -0.47 | -1.41 | 0.181 | 0.921 | 0.948 | 23206 | tags=81%, list=42%, signal=141% | |
346 | POSITIVE REGULATION OF PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 345 | -0.41 | -1.41 | 0.087 | 0.920 | 0.948 | 20833 | tags=65%, list=38%, signal=104% | |
347 | HISTONE H2B UBIQUITINATION | 19 | -0.52 | -1.41 | 0.120 | 0.918 | 0.948 | 20112 | tags=74%, list=37%, signal=117% | |
348 | MITOCHONDRIAL RNA METABOLIC PROCESS | 51 | -0.42 | -1.41 | 0.075 | 0.915 | 0.948 | 19409 | tags=63%, list=35%, signal=97% | |
349 | NEGATIVE REGULATION OF G1/S TRANSITION OF MITOTIC CELL CYCLE | 219 | -0.40 | -1.41 | 0.084 | 0.920 | 0.948 | 21273 | tags=64%, list=39%, signal=105% | |
350 | POSITIVE REGULATION OF PROTEOLYSIS INVOLVED IN CELLULAR PROTEIN CATABOLIC PROCESS | 315 | -0.42 | -1.41 | 0.077 | 0.920 | 0.948 | 20632 | tags=65%, list=38%, signal=104% | |
351 | PROTEIN MONOUBIQUITINATION | 101 | -0.43 | -1.41 | 0.041 | 0.918 | 0.948 | 23276 | tags=72%, list=43%, signal=126% | |
352 | IRE1-MEDIATED UNFOLDED PROTEIN RESPONSE | 142 | -0.42 | -1.41 | 0.066 | 0.918 | 0.948 | 21702 | tags=69%, list=40%, signal=114% | |
353 | REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 71 | -0.43 | -1.40 | 0.027 | 0.929 | 0.949 | 8035 | tags=42%, list=15%, signal=49% | |
354 | POSITIVE REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 71 | -0.43 | -1.40 | 0.027 | 0.926 | 0.949 | 8035 | tags=42%, list=15%, signal=49% | |
355 | DEOXYRIBONUCLEOSIDE MONOPHOSPHATE METABOLIC PROCESS | 12 | -0.52 | -1.40 | 0.090 | 0.924 | 0.949 | 20054 | tags=83%, list=37%, signal=132% | |
356 | POSITIVE REGULATION OF MITOCHONDRION ORGANIZATION | 347 | -0.36 | -1.40 | 0.031 | 0.923 | 0.949 | 18509 | tags=52%, list=34%, signal=78% | |
357 | TRNA THREONYLCARBAMOYLADENOSINE METABOLIC PROCESS | 16 | -0.54 | -1.40 | 0.109 | 0.923 | 0.949 | 21424 | tags=88%, list=39%, signal=144% | |
358 | MITOCHONDRIAL TRNA MODIFICATION | 16 | -0.54 | -1.40 | 0.109 | 0.920 | 0.949 | 21424 | tags=88%, list=39%, signal=144% | |
359 | MITOCHONDRIAL RNA MODIFICATION | 16 | -0.54 | -1.40 | 0.109 | 0.918 | 0.949 | 21424 | tags=88%, list=39%, signal=144% | |
360 | SPHINGOID METABOLIC PROCESS | 19 | -0.47 | -1.40 | 0.069 | 0.921 | 0.949 | 17220 | tags=63%, list=31%, signal=92% | |
361 | NEGATIVE REGULATION OF CYCLIN-DEPENDENT PROTEIN SERINE/THREONINE KINASE ACTIVITY | 49 | -0.43 | -1.40 | 0.053 | 0.919 | 0.949 | 19440 | tags=63%, list=36%, signal=98% | |
362 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO ENDOPLASMIC RETICULUM | 281 | -0.47 | -1.40 | 0.183 | 0.918 | 0.949 | 17625 | tags=68%, list=32%, signal=100% | |
363 | NOTCH RECEPTOR PROCESSING | 54 | -0.39 | -1.40 | 0.083 | 0.916 | 0.949 | 9432 | tags=41%, list=17%, signal=49% | |
364 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 44 | -0.37 | -1.40 | 0.092 | 0.919 | 0.951 | 14444 | tags=41%, list=26%, signal=56% | |
365 | TRANSFORMED CELL APOPTOTIC PROCESS | 17 | -0.47 | -1.40 | 0.095 | 0.917 | 0.952 | 18417 | tags=53%, list=34%, signal=80% | |
366 | OXIDOREDUCTION COENZYME METABOLIC PROCESS | 163 | -0.37 | -1.40 | 0.041 | 0.918 | 0.952 | 17101 | tags=49%, list=31%, signal=71% | |
367 | CYTOPLASMIC SEQUESTERING OF PROTEIN | 59 | -0.38 | -1.40 | 0.071 | 0.917 | 0.952 | 18982 | tags=53%, list=35%, signal=80% | |
368 | N-TERMINAL PROTEIN AMINO ACID ACETYLATION | 27 | -0.41 | -1.40 | 0.095 | 0.915 | 0.952 | 15175 | tags=48%, list=28%, signal=67% | |
369 | NEGATIVE REGULATION OF PEPTIDYL-THREONINE PHOSPHORYLATION | 30 | -0.46 | -1.40 | 0.095 | 0.915 | 0.952 | 21460 | tags=70%, list=39%, signal=115% | |
370 | POSITIVE REGULATION OF G2/M TRANSITION OF MITOTIC CELL CYCLE | 28 | -0.45 | -1.40 | 0.054 | 0.917 | 0.952 | 24761 | tags=79%, list=45%, signal=144% | |
371 | REGULATION OF VIRAL BUDDING VIA HOST ESCRT COMPLEX | 5 | -0.73 | -1.40 | 0.076 | 0.920 | 0.953 | 7208 | tags=80%, list=13%, signal=92% | |
372 | ER-ASSOCIATED MISFOLDED PROTEIN CATABOLIC PROCESS | 12 | -0.57 | -1.40 | 0.143 | 0.919 | 0.954 | 15267 | tags=67%, list=28%, signal=92% | |
373 | PROTEIN TARGETING TO ER | 268 | -0.47 | -1.40 | 0.184 | 0.918 | 0.954 | 17625 | tags=69%, list=32%, signal=101% | |
374 | DNA CATABOLIC PROCESS | 39 | -0.47 | -1.40 | 0.094 | 0.917 | 0.954 | 18611 | tags=67%, list=34%, signal=101% | |
375 | POSITIVE REGULATION OF PROTEIN UBIQUITINATION | 322 | -0.41 | -1.40 | 0.090 | 0.915 | 0.954 | 20833 | tags=65%, list=38%, signal=105% | |
376 | ATP SYNTHESIS COUPLED ELECTRON TRANSPORT | 5 | -0.63 | -1.40 | 0.084 | 0.918 | 0.954 | 16851 | tags=80%, list=31%, signal=116% | |
377 | POSITIVE REGULATION OF CELLULAR PROTEIN CATABOLIC PROCESS | 334 | -0.41 | -1.40 | 0.081 | 0.916 | 0.954 | 20632 | tags=64%, list=38%, signal=102% | |
378 | PYRIMIDINE DEOXYRIBONUCLEOTIDE CATABOLIC PROCESS | 20 | -0.45 | -1.39 | 0.099 | 0.914 | 0.954 | 16304 | tags=55%, list=30%, signal=78% | |
379 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE BY P53 CLASS MEDIATOR | 61 | -0.42 | -1.39 | 0.022 | 0.913 | 0.954 | 23895 | tags=70%, list=44%, signal=125% | |
380 | MONOSACCHARIDE CATABOLIC PROCESS | 91 | -0.38 | -1.39 | 0.140 | 0.913 | 0.954 | 10089 | tags=37%, list=18%, signal=46% | |
381 | WHITE FAT CELL DIFFERENTIATION | 16 | -0.51 | -1.39 | 0.109 | 0.911 | 0.954 | 16095 | tags=63%, list=29%, signal=89% | |
382 | POSITIVE REGULATION OF PROTEIN BINDING | 146 | -0.36 | -1.39 | 0.023 | 0.911 | 0.954 | 17769 | tags=47%, list=32%, signal=70% | |
383 | UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS VIA THE MULTIVESICULAR BODY SORTING PATHWAY | 16 | -0.52 | -1.39 | 0.097 | 0.910 | 0.954 | 23364 | tags=88%, list=43%, signal=153% | |
384 | RNA CATABOLIC PROCESS | 501 | -0.41 | -1.39 | 0.116 | 0.909 | 0.954 | 23644 | tags=72%, list=43%, signal=126% | |
385 | VIRAL LATENCY | 28 | -0.47 | -1.39 | 0.089 | 0.907 | 0.954 | 16208 | tags=57%, list=30%, signal=81% | |
386 | ESTABLISHMENT OF VIRAL LATENCY | 28 | -0.47 | -1.39 | 0.089 | 0.905 | 0.954 | 16208 | tags=57%, list=30%, signal=81% | |
387 | SELENOCYSTEINE METABOLIC PROCESS | 212 | -0.49 | -1.39 | 0.196 | 0.909 | 0.955 | 17027 | tags=69%, list=31%, signal=100% | |
388 | ANTEROGRADE AXONAL TRANSPORT | 47 | -0.40 | -1.39 | 0.050 | 0.907 | 0.955 | 20959 | tags=60%, list=38%, signal=97% | |
389 | SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 263 | -0.40 | -1.39 | 0.052 | 0.905 | 0.955 | 21273 | tags=63%, list=39%, signal=103% | |
390 | COTRANSLATIONAL PROTEIN TARGETING TO MEMBRANE | 264 | -0.47 | -1.39 | 0.193 | 0.908 | 0.956 | 17625 | tags=69%, list=32%, signal=101% | |
391 | SELENIUM COMPOUND METABOLIC PROCESS | 266 | -0.45 | -1.39 | 0.204 | 0.907 | 0.956 | 17042 | tags=63%, list=31%, signal=91% | |
392 | ERAD PATHWAY | 160 | -0.40 | -1.39 | 0.057 | 0.908 | 0.956 | 15859 | tags=52%, list=29%, signal=74% | |
393 | VIRAL PROTEIN PROCESSING | 21 | -0.51 | -1.39 | 0.126 | 0.908 | 0.957 | 11952 | tags=62%, list=22%, signal=79% | |
394 | BLOOD VESSEL ENDOTHELIAL CELL DIFFERENTIATION | 15 | -0.46 | -1.39 | 0.085 | 0.910 | 0.957 | 25051 | tags=73%, list=46%, signal=135% | |
395 | NEGATIVE REGULATION OF VIRAL-INDUCED CYTOPLASMIC PATTERN RECOGNITION RECEPTOR SIGNALING PATHWAY | 9 | -0.55 | -1.39 | 0.126 | 0.910 | 0.957 | 5108 | tags=44%, list=9%, signal=49% | |
396 | MITOCHONDRIAL RESPIRATORY CHAIN COMPLEX IV ASSEMBLY | 10 | -0.52 | -1.39 | 0.093 | 0.908 | 0.957 | 15721 | tags=70%, list=29%, signal=98% | |
397 | MITOCHONDRIAL RESPIRATORY CHAIN COMPLEX IV BIOGENESIS | 10 | -0.52 | -1.39 | 0.093 | 0.906 | 0.957 | 15721 | tags=70%, list=29%, signal=98% | |
398 | VIRAL PROCESS | 925 | -0.39 | -1.39 | 0.092 | 0.906 | 0.957 | 19472 | tags=60%, list=36%, signal=92% | |
399 | CELLULAR AMINO ACID METABOLIC PROCESS | 796 | -0.36 | -1.39 | 0.141 | 0.905 | 0.957 | 23419 | tags=61%, list=43%, signal=105% | |
400 | HEXOSE BIOSYNTHETIC PROCESS | 80 | -0.40 | -1.39 | 0.163 | 0.904 | 0.957 | 22787 | tags=65%, list=42%, signal=111% | |
401 | SERINE FAMILY AMINO ACID METABOLIC PROCESS | 269 | -0.45 | -1.39 | 0.204 | 0.904 | 0.957 | 23206 | tags=76%, list=42%, signal=132% | |
402 | ESTABLISHMENT OF MONOPOLAR CELL POLARITY | 8 | -0.59 | -1.39 | 0.085 | 0.903 | 0.957 | 21116 | tags=88%, list=39%, signal=143% | |
403 | REGULATION OF TELOMERASE ACTIVITY | 94 | -0.38 | -1.39 | 0.051 | 0.902 | 0.957 | 23219 | tags=63%, list=42%, signal=109% | |
404 | POSITIVE REGULATION OF PROTEIN TARGETING TO MITOCHONDRION | 192 | -0.35 | -1.39 | 0.038 | 0.903 | 0.958 | 15560 | tags=44%, list=28%, signal=61% | |
405 | NEGATIVE REGULATION OF CAMP-DEPENDENT PROTEIN KINASE ACTIVITY | 15 | -0.50 | -1.39 | 0.093 | 0.901 | 0.958 | 21608 | tags=73%, list=40%, signal=121% | |
406 | EXONUCLEOLYTIC NUCLEAR-TRANSCRIBED MRNA CATABOLIC PROCESS INVOLVED IN DEADENYLATION-DEPENDENT DECAY | 73 | -0.44 | -1.39 | 0.101 | 0.903 | 0.959 | 23171 | tags=74%, list=42%, signal=128% | |
407 | NUCLEOTIDE PHOSPHORYLATION | 124 | -0.37 | -1.38 | 0.082 | 0.903 | 0.959 | 20756 | tags=56%, list=38%, signal=89% | |
408 | GLYCOSYL COMPOUND BIOSYNTHETIC PROCESS | 145 | -0.39 | -1.38 | 0.102 | 0.901 | 0.959 | 20988 | tags=62%, list=38%, signal=100% | |
409 | CHAPERONE-MEDIATED PROTEIN FOLDING | 49 | -0.45 | -1.38 | 0.129 | 0.899 | 0.959 | 20896 | tags=71%, list=38%, signal=116% | |
410 | TUMOR NECROSIS FACTOR-MEDIATED SIGNALING PATHWAY | 273 | -0.37 | -1.38 | 0.038 | 0.900 | 0.959 | 18818 | tags=54%, list=34%, signal=82% | |
411 | CELLULAR RESPONSE TO UNFOLDED PROTEIN | 234 | -0.38 | -1.38 | 0.090 | 0.898 | 0.959 | 21062 | tags=61%, list=39%, signal=98% | |
412 | POSITIVE REGULATION OF FATTY ACID BIOSYNTHETIC PROCESS | 11 | -0.58 | -1.38 | 0.137 | 0.897 | 0.959 | 4646 | tags=36%, list=8%, signal=40% | |
413 | 'DE NOVO' PROTEIN FOLDING | 96 | -0.42 | -1.38 | 0.131 | 0.896 | 0.959 | 25757 | tags=78%, list=47%, signal=147% | |
414 | MITOTIC METAPHASE PLATE CONGRESSION | 56 | -0.45 | -1.38 | 0.102 | 0.895 | 0.959 | 21773 | tags=75%, list=40%, signal=125% | |
415 | NCRNA METABOLIC PROCESS | 668 | -0.40 | -1.38 | 0.070 | 0.893 | 0.959 | 22221 | tags=66%, list=41%, signal=109% | |
416 | ANTIGEN PROCESSING AND PRESENTATION OF ENDOGENOUS PEPTIDE ANTIGEN | 30 | -0.49 | -1.38 | 0.151 | 0.895 | 0.960 | 14736 | tags=57%, list=27%, signal=78% | |
417 | REGULATION OF RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 92 | -0.40 | -1.38 | 0.071 | 0.898 | 0.962 | 18803 | tags=60%, list=34%, signal=91% | |
418 | RNA PHOSPHODIESTER BOND HYDROLYSIS, ENDONUCLEOLYTIC | 52 | -0.41 | -1.38 | 0.033 | 0.898 | 0.962 | 23310 | tags=69%, list=43%, signal=121% | |
419 | ANTEROGRADE SYNAPTIC VESICLE TRANSPORT | 29 | -0.46 | -1.38 | 0.057 | 0.898 | 0.962 | 23707 | tags=76%, list=43%, signal=134% | |
420 | SYNAPTIC VESICLE CYTOSKELETAL TRANSPORT | 29 | -0.46 | -1.38 | 0.057 | 0.895 | 0.962 | 23707 | tags=76%, list=43%, signal=134% | |
421 | SYNAPTIC VESICLE TRANSPORT ALONG MICROTUBULE | 29 | -0.46 | -1.38 | 0.057 | 0.893 | 0.962 | 23707 | tags=76%, list=43%, signal=134% | |
422 | NEGATIVE REGULATION OF CYTOKINESIS | 8 | -0.57 | -1.38 | 0.123 | 0.896 | 0.962 | 16856 | tags=75%, list=31%, signal=108% | |
423 | GLUCOSE METABOLIC PROCESS | 190 | -0.37 | -1.38 | 0.114 | 0.895 | 0.962 | 22787 | tags=61%, list=42%, signal=104% | |
424 | POSITIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 60 | -0.37 | -1.38 | 0.103 | 0.895 | 0.962 | 12304 | tags=40%, list=23%, signal=52% | |
425 | POSITIVE REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 60 | -0.37 | -1.38 | 0.103 | 0.892 | 0.962 | 12304 | tags=40%, list=23%, signal=52% | |
426 | REGULATION OF DENDRITIC CELL DIFFERENTIATION | 17 | -0.52 | -1.38 | 0.135 | 0.891 | 0.962 | 16702 | tags=65%, list=31%, signal=93% | |
427 | CELLULAR RESPONSE TO THYROID HORMONE STIMULUS | 29 | -0.43 | -1.38 | 0.069 | 0.889 | 0.962 | 20137 | tags=59%, list=37%, signal=93% | |
428 | NCRNA PROCESSING | 435 | -0.39 | -1.38 | 0.076 | 0.888 | 0.962 | 22221 | tags=65%, list=41%, signal=109% | |
429 | METAPHASE PLATE CONGRESSION | 66 | -0.44 | -1.38 | 0.120 | 0.892 | 0.962 | 21773 | tags=71%, list=40%, signal=118% | |
430 | ENERGY DERIVATION BY OXIDATION OF ORGANIC COMPOUNDS | 595 | -0.35 | -1.38 | 0.094 | 0.892 | 0.962 | 22787 | tags=58%, list=42%, signal=99% | |
431 | REGULATION OF INTEGRIN-MEDIATED SIGNALING PATHWAY | 17 | -0.50 | -1.38 | 0.098 | 0.891 | 0.962 | 20118 | tags=76%, list=37%, signal=121% | |
432 | REGULATION OF RESPIRATORY SYSTEM PROCESS | 14 | -0.49 | -1.38 | 0.120 | 0.890 | 0.962 | 11550 | tags=50%, list=21%, signal=63% | |
433 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO ORGANELLE | 704 | -0.39 | -1.38 | 0.112 | 0.888 | 0.962 | 20932 | tags=63%, list=38%, signal=101% | |
434 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE I PROMOTER | 34 | -0.41 | -1.38 | 0.113 | 0.889 | 0.963 | 8214 | tags=38%, list=15%, signal=45% | |
435 | NEGATIVE REGULATION OF CELLULAR PROTEIN CATABOLIC PROCESS | 189 | -0.39 | -1.38 | 0.054 | 0.887 | 0.963 | 16700 | tags=52%, list=31%, signal=75% | |
436 | PROTEIN AUTOUBIQUITINATION | 110 | -0.40 | -1.38 | 0.081 | 0.888 | 0.963 | 21607 | tags=64%, list=40%, signal=105% | |
437 | GLYCEROPHOSPHOLIPID CATABOLIC PROCESS | 16 | -0.50 | -1.38 | 0.099 | 0.886 | 0.963 | 13398 | tags=63%, list=25%, signal=83% | |
438 | ESTABLISHMENT OF CELL POLARITY | 97 | -0.36 | -1.38 | 0.026 | 0.884 | 0.963 | 21154 | tags=54%, list=39%, signal=87% | |
439 | FATTY ACID CATABOLIC PROCESS | 104 | -0.41 | -1.38 | 0.106 | 0.885 | 0.963 | 20089 | tags=63%, list=37%, signal=99% | |
440 | ECTODERMAL PLACODE FORMATION | 20 | -0.49 | -1.38 | 0.133 | 0.884 | 0.963 | 12728 | tags=50%, list=23%, signal=65% | |
441 | ECTODERMAL PLACODE DEVELOPMENT | 20 | -0.49 | -1.38 | 0.133 | 0.882 | 0.963 | 12728 | tags=50%, list=23%, signal=65% | |
442 | ECTODERMAL PLACODE MORPHOGENESIS | 20 | -0.49 | -1.38 | 0.133 | 0.880 | 0.963 | 12728 | tags=50%, list=23%, signal=65% | |
443 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO MITOCHONDRION | 280 | -0.36 | -1.37 | 0.038 | 0.880 | 0.964 | 16162 | tags=46%, list=30%, signal=66% | |
444 | APOPTOTIC DNA FRAGMENTATION | 28 | -0.48 | -1.37 | 0.136 | 0.879 | 0.964 | 18611 | tags=68%, list=34%, signal=103% | |
445 | REGULATION OF TELOMERE MAINTENANCE VIA TELOMERASE | 119 | -0.39 | -1.37 | 0.059 | 0.879 | 0.964 | 23271 | tags=65%, list=43%, signal=112% | |
446 | GLYCOLYTIC PROCESS | 64 | -0.40 | -1.37 | 0.165 | 0.879 | 0.964 | 9676 | tags=38%, list=18%, signal=46% | |
447 | MYELOID CELL DEVELOPMENT | 24 | -0.46 | -1.37 | 0.086 | 0.879 | 0.964 | 20931 | tags=67%, list=38%, signal=108% | |
448 | PIGMENT CELL DIFFERENTIATION | 28 | -0.43 | -1.37 | 0.067 | 0.877 | 0.964 | 17854 | tags=54%, list=33%, signal=80% | |
449 | CARDIOLIPIN BIOSYNTHETIC PROCESS | 20 | -0.48 | -1.37 | 0.126 | 0.877 | 0.964 | 16851 | tags=65%, list=31%, signal=94% | |
450 | POLYAMINE BIOSYNTHETIC PROCESS | 13 | -0.51 | -1.37 | 0.128 | 0.875 | 0.964 | 5870 | tags=38%, list=11%, signal=43% | |
451 | POSITIVE REGULATION OF LAMELLIPODIUM ORGANIZATION | 62 | -0.38 | -1.37 | 0.107 | 0.874 | 0.964 | 19435 | tags=52%, list=36%, signal=80% | |
452 | NEGATIVE REGULATION OF CELLULAR CATABOLIC PROCESS | 344 | -0.36 | -1.37 | 0.031 | 0.872 | 0.964 | 15125 | tags=46%, list=28%, signal=63% | |
453 | NUCLEOSIDE BIOSYNTHETIC PROCESS | 142 | -0.38 | -1.37 | 0.110 | 0.872 | 0.965 | 20988 | tags=62%, list=38%, signal=100% | |
454 | POSITIVE REGULATION OF CELL CYCLE G2/M PHASE TRANSITION | 31 | -0.44 | -1.37 | 0.096 | 0.874 | 0.965 | 24761 | tags=77%, list=45%, signal=141% | |
455 | NEGATIVE REGULATION OF PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 315 | -0.39 | -1.37 | 0.072 | 0.873 | 0.965 | 23957 | tags=68%, list=44%, signal=121% | |
456 | ESTABLISHMENT OF SPINDLE ORIENTATION | 29 | -0.42 | -1.37 | 0.071 | 0.872 | 0.965 | 26797 | tags=76%, list=49%, signal=149% | |
457 | PROTEIN NEDDYLATION | 13 | -0.55 | -1.37 | 0.120 | 0.870 | 0.965 | 16056 | tags=69%, list=29%, signal=98% | |
458 | ANTIGEN PROCESSING AND PRESENTATION OF EXOGENOUS PEPTIDE ANTIGEN VIA MHC CLASS I, TAP-INDEPENDENT | 30 | -0.52 | -1.37 | 0.144 | 0.868 | 0.965 | 8884 | tags=57%, list=16%, signal=68% | |
459 | MULTI-ORGANISM CELLULAR PROCESS | 939 | -0.39 | -1.37 | 0.094 | 0.869 | 0.965 | 21442 | tags=64%, list=39%, signal=103% | |
460 | HEXOSE METABOLIC PROCESS | 214 | -0.36 | -1.37 | 0.128 | 0.867 | 0.965 | 21159 | tags=57%, list=39%, signal=93% | |
461 | PYRUVATE METABOLIC PROCESS | 129 | -0.37 | -1.37 | 0.116 | 0.866 | 0.965 | 22946 | tags=60%, list=42%, signal=103% | |
462 | CELLULAR RESPONSE TO GLUCOCORTICOID STIMULUS | 21 | -0.46 | -1.37 | 0.125 | 0.864 | 0.965 | 20883 | tags=67%, list=38%, signal=108% | |
463 | REVERSE CHOLESTEROL TRANSPORT | 29 | -0.44 | -1.37 | 0.129 | 0.864 | 0.965 | 16531 | tags=48%, list=30%, signal=69% | |
464 | MEMBRANE FUSION | 196 | -0.40 | -1.37 | 0.069 | 0.864 | 0.965 | 20796 | tags=62%, list=38%, signal=99% | |
465 | NEGATIVE REGULATION OF ERBB SIGNALING PATHWAY | 127 | -0.37 | -1.37 | 0.053 | 0.865 | 0.965 | 23401 | tags=62%, list=43%, signal=108% | |
466 | NEGATIVE REGULATION OF PROTEIN UBIQUITINATION | 304 | -0.39 | -1.37 | 0.077 | 0.864 | 0.965 | 23957 | tags=68%, list=44%, signal=121% | |
467 | NUCLEAR-TRANSCRIBED MRNA CATABOLIC PROCESS, EXONUCLEOLYTIC | 77 | -0.44 | -1.37 | 0.100 | 0.864 | 0.965 | 19932 | tags=68%, list=36%, signal=106% | |
468 | NEGATIVE REGULATION OF T CELL CYTOKINE PRODUCTION | 23 | -0.50 | -1.37 | 0.114 | 0.863 | 0.965 | 7049 | tags=35%, list=13%, signal=40% | |
469 | MAINTENANCE OF PROTEIN LOCALIZATION IN ORGANELLE | 58 | -0.41 | -1.37 | 0.033 | 0.862 | 0.965 | 21548 | tags=66%, list=39%, signal=108% | |
470 | POSITIVE REGULATION OF NUCLEAR CELL CYCLE DNA REPLICATION | 15 | -0.51 | -1.37 | 0.130 | 0.863 | 0.968 | 2700 | tags=33%, list=5%, signal=35% | |
471 | PROTEIN TRANSMEMBRANE TRANSPORT | 83 | -0.41 | -1.37 | 0.107 | 0.863 | 0.968 | 20533 | tags=64%, list=38%, signal=102% | |
472 | POSITIVE REGULATION OF TRANSCRIPTION INITIATION FROM RNA POLYMERASE II PROMOTER | 11 | -0.50 | -1.37 | 0.099 | 0.864 | 0.968 | 24508 | tags=82%, list=45%, signal=148% | |
473 | PYRIMIDINE DEOXYRIBONUCLEOTIDE METABOLIC PROCESS | 23 | -0.43 | -1.37 | 0.091 | 0.863 | 0.968 | 21468 | tags=65%, list=39%, signal=107% | |
474 | PROLINE TRANSMEMBRANE TRANSPORT | 7 | -0.62 | -1.37 | 0.094 | 0.866 | 0.968 | 20980 | tags=100%, list=38%, signal=162% | |
475 | CELLULAR BIOGENIC AMINE METABOLIC PROCESS | 329 | -0.34 | -1.37 | 0.076 | 0.867 | 0.968 | 23115 | tags=59%, list=42%, signal=101% | |
476 | CELLULAR AMINE METABOLIC PROCESS | 329 | -0.34 | -1.37 | 0.076 | 0.865 | 0.968 | 23115 | tags=59%, list=42%, signal=101% | |
477 | REGULATION OF MITOCHONDRION ORGANIZATION | 447 | -0.34 | -1.37 | 0.044 | 0.864 | 0.968 | 18509 | tags=50%, list=34%, signal=75% | |
478 | XENOBIOTIC CATABOLIC PROCESS | 10 | -0.59 | -1.37 | 0.129 | 0.863 | 0.968 | 18349 | tags=90%, list=34%, signal=135% | |
479 | NEGATIVE REGULATION OF INTERLEUKIN-8 PRODUCTION | 42 | -0.39 | -1.36 | 0.064 | 0.862 | 0.969 | 19583 | tags=50%, list=36%, signal=78% | |
480 | PHOSPHOLIPID CATABOLIC PROCESS | 26 | -0.44 | -1.36 | 0.091 | 0.862 | 0.969 | 13398 | tags=50%, list=25%, signal=66% | |
481 | MITOCHONDRION DISTRIBUTION | 13 | -0.49 | -1.36 | 0.120 | 0.860 | 0.969 | 22697 | tags=77%, list=42%, signal=131% | |
482 | ADP METABOLIC PROCESS | 72 | -0.38 | -1.36 | 0.157 | 0.862 | 0.969 | 9676 | tags=36%, list=18%, signal=44% | |
483 | HISTONE H3 ACETYLATION | 91 | -0.37 | -1.36 | 0.123 | 0.865 | 0.969 | 20339 | tags=59%, list=37%, signal=94% | |
484 | CELLULAR MODIFIED AMINO ACID CATABOLIC PROCESS | 21 | -0.47 | -1.36 | 0.155 | 0.864 | 0.969 | 19116 | tags=67%, list=35%, signal=102% | |
485 | POSITIVE REGULATION OF TRANSCRIPTION ELONGATION FROM RNA POLYMERASE II PROMOTER | 28 | -0.45 | -1.36 | 0.055 | 0.862 | 0.969 | 15797 | tags=61%, list=29%, signal=85% | |
486 | ANTIGEN PROCESSING AND PRESENTATION OF PEPTIDE ANTIGEN VIA MHC CLASS I | 213 | -0.41 | -1.36 | 0.093 | 0.861 | 0.969 | 19835 | tags=63%, list=36%, signal=99% | |
487 | NUCLEOSIDE DIPHOSPHATE METABOLIC PROCESS | 125 | -0.36 | -1.36 | 0.097 | 0.860 | 0.969 | 20756 | tags=54%, list=38%, signal=87% | |
488 | GALACTOSE CATABOLIC PROCESS | 12 | -0.51 | -1.36 | 0.093 | 0.862 | 0.969 | 22787 | tags=83%, list=42%, signal=143% | |
489 | NEGATIVE REGULATION OF EPIDERMAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 126 | -0.37 | -1.36 | 0.051 | 0.865 | 0.969 | 23401 | tags=62%, list=43%, signal=108% | |
490 | POSITIVE REGULATION OF TRANSCRIPTION OF NUCLEAR LARGE RRNA TRANSCRIPT FROM RNA POLYMERASE I PROMOTER | 17 | -0.47 | -1.36 | 0.128 | 0.864 | 0.969 | 10424 | tags=47%, list=19%, signal=58% | |
491 | GOLGI VESICLE BUDDING | 32 | -0.47 | -1.36 | 0.115 | 0.863 | 0.969 | 23983 | tags=78%, list=44%, signal=139% | |
492 | HISTONE UBIQUITINATION | 77 | -0.43 | -1.36 | 0.105 | 0.861 | 0.969 | 23276 | tags=73%, list=43%, signal=126% | |
493 | REGULATION OF RESPONSE TO EXTRACELLULAR STIMULUS | 263 | -0.35 | -1.36 | 0.022 | 0.862 | 0.969 | 18627 | tags=52%, list=34%, signal=78% | |
494 | REGULATION OF RESPONSE TO NUTRIENT LEVELS | 263 | -0.35 | -1.36 | 0.022 | 0.860 | 0.969 | 18627 | tags=52%, list=34%, signal=78% | |
495 | EPIBOLY | 31 | -0.41 | -1.36 | 0.121 | 0.864 | 0.969 | 10215 | tags=39%, list=19%, signal=48% | |
496 | NEGATIVE REGULATION OF RUFFLE ASSEMBLY | 12 | -0.48 | -1.36 | 0.147 | 0.865 | 0.969 | 14116 | tags=50%, list=26%, signal=67% | |
497 | NEGATIVE REGULATION OF TELOMERASE ACTIVITY | 39 | -0.40 | -1.36 | 0.108 | 0.866 | 0.969 | 8872 | tags=36%, list=16%, signal=43% | |
498 | GLYCOGEN CATABOLIC PROCESS | 44 | -0.42 | -1.36 | 0.101 | 0.865 | 0.969 | 19181 | tags=61%, list=35%, signal=94% | |
499 | NEGATIVE REGULATION OF HIPPO SIGNALING | 23 | -0.43 | -1.36 | 0.069 | 0.865 | 0.969 | 14620 | tags=48%, list=27%, signal=65% | |
500 | RETROGRADE TRANSPORT, ENDOSOME TO PLASMA MEMBRANE | 33 | -0.45 | -1.36 | 0.144 | 0.863 | 0.969 | 20753 | tags=67%, list=38%, signal=107% | |
501 | ALPHA-AMINO ACID METABOLIC PROCESS | 594 | -0.36 | -1.36 | 0.180 | 0.863 | 0.969 | 23419 | tags=61%, list=43%, signal=105% | |
502 | FOLIC ACID METABOLIC PROCESS | 39 | -0.41 | -1.36 | 0.111 | 0.865 | 0.969 | 18055 | tags=49%, list=33%, signal=73% | |
503 | REGULATION OF ATP BIOSYNTHETIC PROCESS | 13 | -0.47 | -1.36 | 0.082 | 0.864 | 0.969 | 19751 | tags=54%, list=36%, signal=84% | |
504 | DETERMINATION OF DIGESTIVE TRACT LEFT/RIGHT ASYMMETRY | 16 | -0.52 | -1.36 | 0.147 | 0.864 | 0.969 | 17561 | tags=69%, list=32%, signal=101% | |
505 | REGULATION OF PROTEIN HOMODIMERIZATION ACTIVITY | 40 | -0.40 | -1.35 | 0.065 | 0.867 | 0.969 | 10428 | tags=40%, list=19%, signal=49% | |
506 | POSITIVE REGULATION OF TYPE I INTERFERON PRODUCTION | 180 | -0.37 | -1.35 | 0.026 | 0.870 | 0.969 | 15474 | tags=48%, list=28%, signal=66% | |
507 | PROTEIN LOCALIZATION TO MEMBRANE | 767 | -0.35 | -1.35 | 0.126 | 0.869 | 0.969 | 22652 | tags=59%, list=41%, signal=99% | |
508 | LONG-TERM SYNAPTIC POTENTIATION | 23 | -0.42 | -1.35 | 0.166 | 0.868 | 0.969 | 18096 | tags=52%, list=33%, signal=78% | |
509 | NEGATIVE REGULATION OF NUCLEOTIDE CATABOLIC PROCESS | 10 | -0.52 | -1.35 | 0.120 | 0.867 | 0.969 | 8742 | tags=40%, list=16%, signal=48% | |
510 | PYRIDINE-CONTAINING COMPOUND METABOLIC PROCESS | 159 | -0.36 | -1.35 | 0.075 | 0.865 | 0.969 | 17101 | tags=47%, list=31%, signal=68% | |
511 | STEM CELL DIVISION | 47 | -0.39 | -1.35 | 0.107 | 0.864 | 0.969 | 15902 | tags=49%, list=29%, signal=69% | |
512 | HISTONE H3-K27 METHYLATION | 10 | -0.50 | -1.35 | 0.134 | 0.863 | 0.969 | 1354 | tags=30%, list=2%, signal=31% | |
513 | PLATELET AGGREGATION | 88 | -0.38 | -1.35 | 0.144 | 0.871 | 0.969 | 12510 | tags=39%, list=23%, signal=50% | |
514 | REGULATION OF VACUOLE ORGANIZATION | 81 | -0.43 | -1.35 | 0.045 | 0.870 | 0.969 | 25770 | tags=80%, list=47%, signal=152% | |
515 | SYMBIOSIS, ENCOMPASSING MUTUALISM THROUGH PARASITISM | 1017 | -0.38 | -1.35 | 0.102 | 0.869 | 0.969 | 21442 | tags=62%, list=39%, signal=100% | |
516 | INTERSPECIES INTERACTION BETWEEN ORGANISMS | 1017 | -0.38 | -1.35 | 0.102 | 0.867 | 0.969 | 21442 | tags=62%, list=39%, signal=100% | |
517 | RESPONSE TO UNFOLDED PROTEIN | 271 | -0.36 | -1.35 | 0.112 | 0.866 | 0.969 | 17858 | tags=53%, list=33%, signal=78% | |
518 | NECROTIC CELL DEATH | 69 | -0.40 | -1.35 | 0.126 | 0.868 | 0.969 | 18782 | tags=59%, list=34%, signal=90% | |
519 | TETRAPYRROLE METABOLIC PROCESS | 86 | -0.38 | -1.35 | 0.142 | 0.866 | 0.969 | 20140 | tags=58%, list=37%, signal=92% | |
520 | POSITIVE REGULATION OF SUPEROXIDE ANION GENERATION | 9 | -0.58 | -1.35 | 0.138 | 0.866 | 0.969 | 11512 | tags=56%, list=21%, signal=70% | |
521 | PROGRAMMED NECROTIC CELL DEATH | 68 | -0.40 | -1.35 | 0.126 | 0.866 | 0.969 | 18530 | tags=59%, list=34%, signal=89% | |
522 | NEGATIVE REGULATION OF CALCIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 47 | -0.38 | -1.35 | 0.094 | 0.865 | 0.969 | 20611 | tags=55%, list=38%, signal=89% | |
523 | NEGATIVE REGULATION OF CALCIUM ION TRANSMEMBRANE TRANSPORT | 47 | -0.38 | -1.35 | 0.094 | 0.863 | 0.969 | 20611 | tags=55%, list=38%, signal=89% | |
524 | REGULATION OF AUTOPHAGY | 419 | -0.35 | -1.35 | 0.007 | 0.862 | 0.969 | 19453 | tags=52%, list=36%, signal=80% | |
525 | NUCLEOSIDE DIPHOSPHATE PHOSPHORYLATION | 88 | -0.37 | -1.35 | 0.131 | 0.861 | 0.969 | 19443 | tags=51%, list=36%, signal=79% | |
526 | NUCLEOBASE-CONTAINING COMPOUND CATABOLIC PROCESS | 689 | -0.38 | -1.35 | 0.099 | 0.860 | 0.969 | 22621 | tags=64%, list=41%, signal=108% | |
527 | DNA DAMAGE RESPONSE, SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 204 | -0.39 | -1.35 | 0.096 | 0.858 | 0.969 | 19567 | tags=58%, list=36%, signal=91% | |
528 | MITOTIC DNA DAMAGE CHECKPOINT | 198 | -0.39 | -1.35 | 0.108 | 0.857 | 0.969 | 21273 | tags=63%, list=39%, signal=102% | |
529 | POSITIVE REGULATION OF PROTEIN CATABOLIC PROCESS | 456 | -0.38 | -1.35 | 0.075 | 0.856 | 0.969 | 20632 | tags=61%, list=38%, signal=96% | |
530 | REGULATION OF TRANSCRIPTION INITIATION FROM RNA POLYMERASE II PROMOTER | 35 | -0.41 | -1.35 | 0.058 | 0.856 | 0.969 | 24508 | tags=69%, list=45%, signal=124% | |
531 | NEGATIVE REGULATION OF RELEASE OF SEQUESTERED CALCIUM ION INTO CYTOSOL | 24 | -0.44 | -1.35 | 0.136 | 0.854 | 0.969 | 19515 | tags=63%, list=36%, signal=97% | |
532 | NEGATIVE REGULATION OF RYANODINE-SENSITIVE CALCIUM-RELEASE CHANNEL ACTIVITY | 24 | -0.44 | -1.35 | 0.136 | 0.853 | 0.969 | 19515 | tags=63%, list=36%, signal=97% | |
533 | INOSITOL PHOSPHATE CATABOLIC PROCESS | 19 | -0.50 | -1.35 | 0.119 | 0.853 | 0.969 | 18246 | tags=74%, list=33%, signal=111% | |
534 | POSITIVE REGULATION OF TOR SIGNALING | 53 | -0.39 | -1.35 | 0.118 | 0.853 | 0.969 | 21836 | tags=60%, list=40%, signal=100% | |
535 | NEGATIVE REGULATION OF PROTEOLYSIS INVOLVED IN CELLULAR PROTEIN CATABOLIC PROCESS | 181 | -0.38 | -1.35 | 0.071 | 0.854 | 0.969 | 16700 | tags=51%, list=31%, signal=73% | |
536 | PROTEIN TARGETING | 768 | -0.38 | -1.35 | 0.113 | 0.858 | 0.969 | 21013 | tags=60%, list=38%, signal=97% | |
537 | RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 469 | -0.36 | -1.35 | 0.071 | 0.861 | 0.969 | 20480 | tags=57%, list=37%, signal=90% | |
538 | DEATH-INDUCING SIGNALING COMPLEX ASSEMBLY | 12 | -0.51 | -1.34 | 0.141 | 0.860 | 0.969 | 7202 | tags=42%, list=13%, signal=48% | |
539 | TELOMERE MAINTENANCE IN RESPONSE TO DNA DAMAGE | 12 | -0.50 | -1.34 | 0.133 | 0.858 | 0.969 | 8705 | tags=42%, list=16%, signal=50% | |
540 | KETONE BIOSYNTHETIC PROCESS | 31 | -0.40 | -1.34 | 0.099 | 0.862 | 0.969 | 13145 | tags=45%, list=24%, signal=59% | |
541 | 'DE NOVO' POSTTRANSLATIONAL PROTEIN FOLDING | 80 | -0.42 | -1.34 | 0.156 | 0.863 | 0.969 | 26295 | tags=79%, list=48%, signal=151% | |
542 | REGULATION OF PROTEIN BINDING | 289 | -0.33 | -1.34 | 0.026 | 0.864 | 0.969 | 16315 | tags=43%, list=30%, signal=60% | |
543 | MITOTIC SPINDLE ORGANIZATION | 106 | -0.38 | -1.34 | 0.056 | 0.867 | 0.969 | 21547 | tags=63%, list=39%, signal=104% | |
544 | WOUND HEALING, SPREADING OF CELLS | 29 | -0.41 | -1.34 | 0.128 | 0.873 | 0.970 | 10215 | tags=38%, list=19%, signal=47% | |
545 | EPIBOLY INVOLVED IN WOUND HEALING | 29 | -0.41 | -1.34 | 0.128 | 0.872 | 0.970 | 10215 | tags=38%, list=19%, signal=47% | |
546 | PROTEIN FOLDING | 312 | -0.38 | -1.34 | 0.134 | 0.871 | 0.970 | 25501 | tags=71%, list=47%, signal=132% | |
547 | INTRACELLULAR PROTEIN TRANSMEMBRANE IMPORT | 61 | -0.42 | -1.34 | 0.128 | 0.869 | 0.970 | 20533 | tags=67%, list=38%, signal=108% | |
548 | AXO-DENDRITIC TRANSPORT | 61 | -0.38 | -1.34 | 0.063 | 0.869 | 0.970 | 23921 | tags=64%, list=44%, signal=114% | |
549 | RIBOSOME ASSEMBLY | 42 | -0.42 | -1.34 | 0.113 | 0.868 | 0.970 | 17272 | tags=57%, list=32%, signal=83% | |
550 | ATP GENERATION FROM ADP | 67 | -0.38 | -1.34 | 0.161 | 0.868 | 0.970 | 9676 | tags=36%, list=18%, signal=43% | |
551 | PROTEIN MATURATION BY PROTEIN FOLDING | 12 | -0.56 | -1.34 | 0.145 | 0.868 | 0.970 | 17627 | tags=83%, list=32%, signal=123% | |
552 | RIBONUCLEOSIDE BIOSYNTHETIC PROCESS | 110 | -0.38 | -1.34 | 0.166 | 0.866 | 0.970 | 20740 | tags=60%, list=38%, signal=96% | |
553 | RNA-DEPENDENT DNA REPLICATION | 46 | -0.43 | -1.34 | 0.109 | 0.865 | 0.970 | 11631 | tags=46%, list=21%, signal=58% | |
554 | REGULATION OF PROTEIN TARGETING TO MITOCHONDRION | 209 | -0.34 | -1.34 | 0.062 | 0.864 | 0.970 | 15560 | tags=43%, list=28%, signal=60% | |
555 | GENERATION OF PRECURSOR METABOLITES AND ENERGY | 728 | -0.33 | -1.34 | 0.124 | 0.866 | 0.970 | 20922 | tags=53%, list=38%, signal=84% | |
556 | NUCLEUS ORGANIZATION | 237 | -0.36 | -1.34 | 0.031 | 0.864 | 0.970 | 22528 | tags=58%, list=41%, signal=98% | |
557 | PYRIMIDINE NUCLEOSIDE BIOSYNTHETIC PROCESS | 40 | -0.42 | -1.34 | 0.102 | 0.863 | 0.970 | 21380 | tags=70%, list=39%, signal=115% | |
558 | PURINE NUCLEOSIDE BIOSYNTHETIC PROCESS | 98 | -0.38 | -1.34 | 0.169 | 0.862 | 0.970 | 20740 | tags=60%, list=38%, signal=97% | |
559 | PURINE RIBONUCLEOSIDE BIOSYNTHETIC PROCESS | 98 | -0.38 | -1.34 | 0.169 | 0.861 | 0.970 | 20740 | tags=60%, list=38%, signal=97% | |
560 | ESTABLISHMENT OF APICAL/BASAL CELL POLARITY | 7 | -0.60 | -1.34 | 0.119 | 0.861 | 0.970 | 20506 | tags=86%, list=38%, signal=137% | |
561 | INNER MITOCHONDRIAL MEMBRANE ORGANIZATION | 25 | -0.45 | -1.34 | 0.164 | 0.862 | 0.970 | 23921 | tags=76%, list=44%, signal=135% | |
562 | SYNAPTIC VESICLE TRANSPORT | 98 | -0.37 | -1.34 | 0.035 | 0.861 | 0.970 | 16426 | tags=46%, list=30%, signal=66% | |
563 | ESTABLISHMENT OF SYNAPTIC VESICLE LOCALIZATION | 98 | -0.37 | -1.34 | 0.035 | 0.860 | 0.970 | 16426 | tags=46%, list=30%, signal=66% | |
564 | 2'-DEOXYRIBONUCLEOTIDE METABOLIC PROCESS | 43 | -0.40 | -1.34 | 0.111 | 0.859 | 0.970 | 16304 | tags=51%, list=30%, signal=73% | |
565 | DEOXYRIBOSE PHOSPHATE METABOLIC PROCESS | 43 | -0.40 | -1.34 | 0.111 | 0.857 | 0.970 | 16304 | tags=51%, list=30%, signal=73% | |
566 | REGULATION OF RNA STABILITY | 324 | -0.37 | -1.34 | 0.125 | 0.858 | 0.970 | 20712 | tags=59%, list=38%, signal=94% | |
567 | SHORT-CHAIN FATTY ACID CATABOLIC PROCESS | 13 | -0.53 | -1.34 | 0.161 | 0.857 | 0.970 | 22394 | tags=77%, list=41%, signal=130% | |
568 | NEGATIVE REGULATION OF ENDOPLASMIC RETICULUM STRESS-INDUCED INTRINSIC APOPTOTIC SIGNALING PATHWAY | 26 | -0.43 | -1.34 | 0.151 | 0.855 | 0.970 | 17468 | tags=58%, list=32%, signal=85% | |
569 | AMINE METABOLIC PROCESS | 341 | -0.33 | -1.34 | 0.089 | 0.854 | 0.970 | 24425 | tags=60%, list=45%, signal=109% | |
570 | NEGATIVE REGULATION OF ENDOPLASMIC RETICULUM UNFOLDED PROTEIN RESPONSE | 24 | -0.44 | -1.34 | 0.162 | 0.853 | 0.970 | 20833 | tags=71%, list=38%, signal=114% | |
571 | RETROGRADE PROTEIN TRANSPORT, ER TO CYTOSOL | 38 | -0.43 | -1.34 | 0.178 | 0.856 | 0.970 | 15730 | tags=58%, list=29%, signal=81% | |
572 | POSITIVE REGULATION OF VESICLE FUSION | 16 | -0.50 | -1.33 | 0.138 | 0.856 | 0.970 | 16328 | tags=56%, list=30%, signal=80% | |
573 | URETER DEVELOPMENT | 9 | -0.48 | -1.33 | 0.145 | 0.859 | 0.971 | 14059 | tags=56%, list=26%, signal=75% | |
574 | NEGATIVE REGULATION OF RECEPTOR INTERNALIZATION | 14 | -0.53 | -1.33 | 0.145 | 0.858 | 0.971 | 13329 | tags=64%, list=24%, signal=85% | |
575 | INTRINSIC APOPTOTIC SIGNALING PATHWAY | 293 | -0.36 | -1.33 | 0.029 | 0.858 | 0.971 | 17851 | tags=52%, list=33%, signal=77% | |
576 | MRNA 3'-END PROCESSING BY STEM-LOOP BINDING AND CLEAVAGE | 11 | -0.54 | -1.33 | 0.156 | 0.857 | 0.971 | 16647 | tags=73%, list=30%, signal=105% | |
577 | REGULATION OF TELOMERE MAINTENANCE VIA TELOMERE LENGTHENING | 133 | -0.36 | -1.33 | 0.090 | 0.858 | 0.971 | 23271 | tags=60%, list=43%, signal=104% | |
578 | POSITIVE REGULATION OF GRANULOCYTE CHEMOTAXIS | 31 | -0.44 | -1.33 | 0.155 | 0.857 | 0.971 | 19058 | tags=55%, list=35%, signal=84% | |
579 | REGULATION OF CYTOPLASMIC TRANSLATION | 25 | -0.44 | -1.33 | 0.146 | 0.856 | 0.971 | 19703 | tags=68%, list=36%, signal=106% | |
580 | NUCLEOSIDE PHOSPHATE BIOSYNTHETIC PROCESS | 229 | -0.34 | -1.33 | 0.101 | 0.855 | 0.971 | 21153 | tags=55%, list=39%, signal=89% | |
581 | POSITIVE REGULATION OF PROTEIN SUMOYLATION | 17 | -0.47 | -1.33 | 0.099 | 0.855 | 0.971 | 6078 | tags=41%, list=11%, signal=46% | |
582 | POSITIVE REGULATION OF CELL AGING | 25 | -0.43 | -1.33 | 0.128 | 0.854 | 0.971 | 6367 | tags=36%, list=12%, signal=41% | |
583 | MYELIN MAINTENANCE | 23 | -0.48 | -1.33 | 0.188 | 0.853 | 0.971 | 18817 | tags=70%, list=34%, signal=106% | |
584 | VIRAL RELEASE FROM HOST CELL | 20 | -0.51 | -1.33 | 0.185 | 0.854 | 0.971 | 6798 | tags=50%, list=12%, signal=57% | |
585 | RESPONSE TO DEFENSES OF OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 12 | -0.51 | -1.33 | 0.126 | 0.852 | 0.971 | 7725 | tags=42%, list=14%, signal=49% | |
586 | RESPONSE TO HOST DEFENSES | 12 | -0.51 | -1.33 | 0.126 | 0.851 | 0.971 | 7725 | tags=42%, list=14%, signal=49% | |
587 | RESPONSE TO HOST | 12 | -0.51 | -1.33 | 0.126 | 0.849 | 0.971 | 7725 | tags=42%, list=14%, signal=49% | |
588 | REGULATION OF MRNA STABILITY | 321 | -0.37 | -1.33 | 0.127 | 0.848 | 0.971 | 20712 | tags=59%, list=38%, signal=94% | |
589 | TRNA METABOLIC PROCESS | 309 | -0.40 | -1.33 | 0.108 | 0.847 | 0.971 | 17887 | tags=57%, list=33%, signal=84% | |
590 | REGULATION OF TOR SIGNALING | 144 | -0.35 | -1.33 | 0.066 | 0.847 | 0.972 | 23393 | tags=59%, list=43%, signal=103% | |
591 | COPI-COATED VESICLE BUDDING | 30 | -0.46 | -1.33 | 0.142 | 0.847 | 0.972 | 23983 | tags=77%, list=44%, signal=136% | |
592 | GOLGI TRANSPORT VESICLE COATING | 30 | -0.46 | -1.33 | 0.142 | 0.846 | 0.972 | 23983 | tags=77%, list=44%, signal=136% | |
593 | COPI COATING OF GOLGI VESICLE | 30 | -0.46 | -1.33 | 0.142 | 0.845 | 0.972 | 23983 | tags=77%, list=44%, signal=136% | |
594 | POLYSACCHARIDE CATABOLIC PROCESS | 45 | -0.42 | -1.33 | 0.127 | 0.844 | 0.972 | 19181 | tags=60%, list=35%, signal=92% | |
595 | GLUCAN CATABOLIC PROCESS | 45 | -0.42 | -1.33 | 0.127 | 0.842 | 0.972 | 19181 | tags=60%, list=35%, signal=92% | |
596 | CELLULAR POLYSACCHARIDE CATABOLIC PROCESS | 45 | -0.42 | -1.33 | 0.127 | 0.841 | 0.972 | 19181 | tags=60%, list=35%, signal=92% | |
597 | PHOSPHATIDYLCHOLINE ACYL-CHAIN REMODELING | 51 | -0.38 | -1.33 | 0.092 | 0.841 | 0.972 | 24138 | tags=67%, list=44%, signal=119% | |
598 | MITOTIC DNA INTEGRITY CHECKPOINT | 210 | -0.37 | -1.33 | 0.124 | 0.844 | 0.972 | 21273 | tags=60%, list=39%, signal=99% | |
599 | FATTY ACID ELONGATION | 16 | -0.48 | -1.33 | 0.131 | 0.843 | 0.972 | 19619 | tags=69%, list=36%, signal=107% | |
600 | REGULATION OF INTERLEUKIN-13 PRODUCTION | 28 | -0.43 | -1.33 | 0.141 | 0.842 | 0.972 | 14706 | tags=43%, list=27%, signal=59% | |
601 | DNA DEALKYLATION INVOLVED IN DNA REPAIR | 12 | -0.53 | -1.33 | 0.142 | 0.844 | 0.972 | 23369 | tags=92%, list=43%, signal=160% | |
602 | HETEROCYCLE CATABOLIC PROCESS | 766 | -0.36 | -1.33 | 0.128 | 0.842 | 0.972 | 22621 | tags=62%, list=41%, signal=104% | |
603 | REGULATION OF CHOLESTEROL EFFLUX | 30 | -0.42 | -1.33 | 0.153 | 0.843 | 0.972 | 15149 | tags=50%, list=28%, signal=69% | |
604 | ESTABLISHMENT OF SPINDLE LOCALIZATION | 56 | -0.39 | -1.33 | 0.100 | 0.843 | 0.972 | 26797 | tags=71%, list=49%, signal=140% | |
605 | REGULATION OF PROTEIN UBIQUITINATION | 528 | -0.37 | -1.33 | 0.084 | 0.843 | 0.972 | 20404 | tags=59%, list=37%, signal=93% | |
606 | NUCLEOTIDE-EXCISION REPAIR, DNA INCISION | 76 | -0.42 | -1.33 | 0.163 | 0.844 | 0.972 | 17200 | tags=61%, list=31%, signal=88% | |
607 | NUCLEAR ENVELOPE ORGANIZATION | 152 | -0.37 | -1.33 | 0.054 | 0.843 | 0.972 | 22528 | tags=61%, list=41%, signal=103% | |
608 | PYRIMIDINE NUCLEOTIDE METABOLIC PROCESS | 43 | -0.40 | -1.33 | 0.162 | 0.842 | 0.972 | 21468 | tags=63%, list=39%, signal=103% | |
609 | ANTIGEN PROCESSING AND PRESENTATION OF ENDOGENOUS ANTIGEN | 31 | -0.47 | -1.33 | 0.164 | 0.842 | 0.972 | 14736 | tags=55%, list=27%, signal=75% | |
610 | REGULATION OF CELLULAR PROTEIN CATABOLIC PROCESS | 533 | -0.38 | -1.33 | 0.080 | 0.842 | 0.972 | 20632 | tags=59%, list=38%, signal=93% | |
611 | INTRACELLULAR PROTEIN TRANSMEMBRANE TRANSPORT | 70 | -0.41 | -1.33 | 0.122 | 0.841 | 0.972 | 20533 | tags=64%, list=38%, signal=103% | |
612 | REGULATION OF IMMUNOGLOBULIN SECRETION | 13 | -0.48 | -1.33 | 0.143 | 0.841 | 0.973 | 3502 | tags=38%, list=6%, signal=41% | |
613 | POSITIVE REGULATION OF IMMUNOGLOBULIN SECRETION | 13 | -0.48 | -1.33 | 0.143 | 0.839 | 0.973 | 3502 | tags=38%, list=6%, signal=41% | |
614 | CELL DIVISION | 309 | -0.36 | -1.33 | 0.050 | 0.838 | 0.973 | 26714 | tags=70%, list=49%, signal=135% | |
615 | PROTEIN K48-LINKED UBIQUITINATION | 140 | -0.38 | -1.33 | 0.106 | 0.838 | 0.973 | 17649 | tags=53%, list=32%, signal=78% | |
616 | PURINE RIBONUCLEOTIDE BIOSYNTHETIC PROCESS | 151 | -0.34 | -1.33 | 0.157 | 0.837 | 0.973 | 11613 | tags=37%, list=21%, signal=47% | |
617 | SIGNAL TRANSDUCTION IN RESPONSE TO DNA DAMAGE | 235 | -0.38 | -1.33 | 0.110 | 0.836 | 0.973 | 19567 | tags=57%, list=36%, signal=89% | |
618 | ENDOPLASMIC RETICULUM TO CYTOSOL TRANSPORT | 50 | -0.40 | -1.33 | 0.155 | 0.836 | 0.974 | 19727 | tags=58%, list=36%, signal=91% | |
619 | REGULATION OF UBIQUITIN-PROTEIN TRANSFERASE ACTIVITY | 277 | -0.39 | -1.32 | 0.135 | 0.837 | 0.974 | 20806 | tags=61%, list=38%, signal=99% | |
620 | CARBOHYDRATE DERIVATIVE TRANSPORT | 64 | -0.37 | -1.32 | 0.097 | 0.840 | 0.974 | 18753 | tags=50%, list=34%, signal=76% | |
621 | CARDIOLIPIN METABOLIC PROCESS | 27 | -0.44 | -1.32 | 0.158 | 0.840 | 0.974 | 14697 | tags=56%, list=27%, signal=76% | |
622 | MUSCLE ADAPTATION | 35 | -0.41 | -1.32 | 0.183 | 0.840 | 0.974 | 16694 | tags=51%, list=31%, signal=74% | |
623 | CELLULAR NITROGEN COMPOUND CATABOLIC PROCESS | 772 | -0.36 | -1.32 | 0.132 | 0.839 | 0.974 | 22621 | tags=62%, list=41%, signal=104% | |
624 | REGULATION OF PROTEOLYSIS INVOLVED IN CELLULAR PROTEIN CATABOLIC PROCESS | 506 | -0.38 | -1.32 | 0.086 | 0.838 | 0.974 | 20632 | tags=59%, list=38%, signal=94% | |
625 | PEPTIDE CATABOLIC PROCESS | 27 | -0.44 | -1.32 | 0.152 | 0.838 | 0.974 | 23476 | tags=74%, list=43%, signal=130% | |
626 | REGULATION OF VESICLE FUSION | 25 | -0.44 | -1.32 | 0.182 | 0.836 | 0.974 | 13128 | tags=48%, list=24%, signal=63% | |
627 | NECROPTOTIC PROCESS | 62 | -0.41 | -1.32 | 0.148 | 0.837 | 0.974 | 18530 | tags=60%, list=34%, signal=90% | |
628 | SINGLE-ORGANISM MEMBRANE BUDDING | 192 | -0.38 | -1.32 | 0.098 | 0.836 | 0.974 | 25273 | tags=70%, list=46%, signal=129% | |
629 | SNRNA PROCESSING | 36 | -0.43 | -1.32 | 0.085 | 0.835 | 0.974 | 21754 | tags=69%, list=40%, signal=115% | |
630 | AROMATIC COMPOUND CATABOLIC PROCESS | 788 | -0.36 | -1.32 | 0.128 | 0.834 | 0.974 | 22621 | tags=61%, list=41%, signal=103% | |
631 | REGULATION OF MYELINATION | 27 | -0.41 | -1.32 | 0.083 | 0.833 | 0.974 | 21709 | tags=63%, list=40%, signal=104% | |
632 | REGULATION OF LIGASE ACTIVITY | 271 | -0.39 | -1.32 | 0.135 | 0.832 | 0.974 | 18818 | tags=58%, list=34%, signal=88% | |
633 | NUCLEOTIDE-EXCISION REPAIR | 213 | -0.40 | -1.32 | 0.128 | 0.833 | 0.974 | 20219 | tags=64%, list=37%, signal=101% | |
634 | POSITIVE REGULATION OF BINDING | 222 | -0.33 | -1.32 | 0.041 | 0.833 | 0.974 | 19706 | tags=48%, list=36%, signal=74% | |
635 | PROTEASOME-MEDIATED UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 507 | -0.38 | -1.32 | 0.106 | 0.837 | 0.974 | 19263 | tags=58%, list=35%, signal=89% | |
636 | REGULATION OF PROTEIN HOMOOLIGOMERIZATION | 35 | -0.42 | -1.32 | 0.139 | 0.837 | 0.974 | 20347 | tags=60%, list=37%, signal=96% | |
637 | MRNA METABOLIC PROCESS | 1043 | -0.38 | -1.32 | 0.103 | 0.837 | 0.974 | 23418 | tags=66%, list=43%, signal=113% | |
638 | CELLULAR RESPONSE TO TUMOR NECROSIS FACTOR | 356 | -0.34 | -1.32 | 0.045 | 0.838 | 0.975 | 18818 | tags=49%, list=34%, signal=74% | |
639 | STRIATED MUSCLE ADAPTATION | 30 | -0.42 | -1.32 | 0.181 | 0.839 | 0.975 | 18530 | tags=57%, list=34%, signal=86% | |
640 | RNA PHOSPHODIESTER BOND HYDROLYSIS, EXONUCLEOLYTIC | 55 | -0.43 | -1.32 | 0.102 | 0.838 | 0.975 | 23584 | tags=73%, list=43%, signal=128% | |
641 | REGULATION OF PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 564 | -0.37 | -1.32 | 0.088 | 0.838 | 0.975 | 20404 | tags=58%, list=37%, signal=92% | |
642 | NEGATIVE REGULATION OF CANONICAL WNT SIGNALING PATHWAY | 309 | -0.33 | -1.32 | 0.129 | 0.838 | 0.975 | 20764 | tags=53%, list=38%, signal=85% | |
643 | G1/S TRANSITION OF MITOTIC CELL CYCLE | 309 | -0.35 | -1.32 | 0.138 | 0.838 | 0.975 | 20613 | tags=56%, list=38%, signal=89% | |
644 | CELL CYCLE G1/S PHASE TRANSITION | 309 | -0.35 | -1.32 | 0.138 | 0.837 | 0.975 | 20613 | tags=56%, list=38%, signal=89% | |
645 | VESICLE TARGETING, TO, FROM OR WITHIN GOLGI | 180 | -0.38 | -1.32 | 0.084 | 0.838 | 0.975 | 25273 | tags=69%, list=46%, signal=129% | |
646 | PROTEIN INSERTION INTO MEMBRANE | 27 | -0.38 | -1.32 | 0.140 | 0.836 | 0.975 | 10442 | tags=33%, list=19%, signal=41% | |
647 | NEGATIVE REGULATION OF CYCLIN-DEPENDENT PROTEIN KINASE ACTIVITY | 85 | -0.38 | -1.32 | 0.092 | 0.836 | 0.975 | 23888 | tags=67%, list=44%, signal=119% | |
648 | NAD METABOLIC PROCESS | 103 | -0.37 | -1.32 | 0.138 | 0.834 | 0.975 | 17101 | tags=47%, list=31%, signal=68% | |
649 | IRON ION TRANSPORT | 123 | -0.35 | -1.32 | 0.031 | 0.835 | 0.975 | 14847 | tags=42%, list=27%, signal=58% | |
650 | MEMBRANE BUDDING | 265 | -0.39 | -1.32 | 0.100 | 0.834 | 0.975 | 25281 | tags=70%, list=46%, signal=129% | |
651 | PYRIDINE NUCLEOTIDE METABOLIC PROCESS | 143 | -0.35 | -1.32 | 0.095 | 0.832 | 0.975 | 17101 | tags=46%, list=31%, signal=67% | |
652 | NICOTINAMIDE NUCLEOTIDE METABOLIC PROCESS | 143 | -0.35 | -1.32 | 0.095 | 0.831 | 0.975 | 17101 | tags=46%, list=31%, signal=67% | |
653 | REGULATION OF DENDRITIC CELL CHEMOTAXIS | 11 | -0.53 | -1.32 | 0.171 | 0.830 | 0.975 | 22043 | tags=82%, list=40%, signal=137% | |
654 | POSITIVE REGULATION OF DENDRITIC CELL CHEMOTAXIS | 11 | -0.53 | -1.32 | 0.171 | 0.829 | 0.975 | 22043 | tags=82%, list=40%, signal=137% | |
655 | POSITIVE REGULATION OF NFAT PROTEIN IMPORT INTO NUCLEUS | 23 | -0.42 | -1.32 | 0.151 | 0.828 | 0.975 | 22671 | tags=61%, list=41%, signal=104% | |
656 | MRNA POLYADENYLATION | 57 | -0.43 | -1.32 | 0.138 | 0.827 | 0.975 | 18099 | tags=65%, list=33%, signal=97% | |
657 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO STRESS | 146 | -0.35 | -1.32 | 0.118 | 0.830 | 0.975 | 23082 | tags=58%, list=42%, signal=100% | |
658 | PTERIDINE-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 9 | -0.56 | -1.31 | 0.155 | 0.831 | 0.975 | 4174 | tags=44%, list=8%, signal=48% | |
659 | PYRIMIDINE-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 42 | -0.41 | -1.31 | 0.124 | 0.830 | 0.975 | 21380 | tags=67%, list=39%, signal=109% | |
660 | REGULATION OF PEPTIDYL-THREONINE PHOSPHORYLATION | 70 | -0.37 | -1.31 | 0.089 | 0.830 | 0.976 | 21479 | tags=59%, list=39%, signal=96% | |
661 | NEGATIVE REGULATION OF RESPONSE TO EXTRACELLULAR STIMULUS | 61 | -0.35 | -1.31 | 0.151 | 0.830 | 0.976 | 14677 | tags=46%, list=27%, signal=63% | |
662 | NEGATIVE REGULATION OF RESPONSE TO NUTRIENT LEVELS | 61 | -0.35 | -1.31 | 0.151 | 0.828 | 0.976 | 14677 | tags=46%, list=27%, signal=63% | |
663 | REGULATION OF AUTOPHAGOSOME ASSEMBLY | 70 | -0.42 | -1.31 | 0.052 | 0.831 | 0.976 | 18627 | tags=63%, list=34%, signal=95% | |
664 | STIMULATORY C-TYPE LECTIN RECEPTOR SIGNALING PATHWAY | 289 | -0.37 | -1.31 | 0.104 | 0.831 | 0.976 | 20868 | tags=59%, list=38%, signal=95% | |
665 | VESICLE TARGETING | 205 | -0.38 | -1.31 | 0.088 | 0.830 | 0.976 | 25273 | tags=70%, list=46%, signal=129% | |
666 | REGULATION OF TYPE I INTERFERON PRODUCTION | 263 | -0.36 | -1.31 | 0.042 | 0.830 | 0.976 | 16283 | tags=48%, list=30%, signal=68% | |
667 | OOGENESIS | 28 | -0.40 | -1.31 | 0.125 | 0.829 | 0.976 | 1978 | tags=21%, list=4%, signal=22% | |
668 | REGULATION OF VIRAL RELEASE FROM HOST CELL | 71 | -0.39 | -1.31 | 0.101 | 0.831 | 0.976 | 24565 | tags=69%, list=45%, signal=125% | |
669 | RIBONUCLEOTIDE BIOSYNTHETIC PROCESS | 159 | -0.34 | -1.31 | 0.165 | 0.831 | 0.976 | 19977 | tags=50%, list=37%, signal=79% | |
670 | REGULATION OF SULFUR METABOLIC PROCESS | 44 | -0.44 | -1.31 | 0.144 | 0.830 | 0.976 | 23703 | tags=77%, list=43%, signal=136% | |
671 | MITOCHONDRIAL MEMBRANE ORGANIZATION | 174 | -0.36 | -1.31 | 0.085 | 0.830 | 0.976 | 24049 | tags=64%, list=44%, signal=115% | |
672 | REGULATION OF EXECUTION PHASE OF APOPTOSIS | 52 | -0.37 | -1.31 | 0.089 | 0.830 | 0.977 | 17851 | tags=50%, list=33%, signal=74% | |
673 | NUCLEAR-TRANSCRIBED MRNA CATABOLIC PROCESS, DEADENYLATION-DEPENDENT DECAY | 134 | -0.40 | -1.31 | 0.140 | 0.831 | 0.977 | 23171 | tags=70%, list=42%, signal=121% | |
674 | NUCLEAR-TRANSCRIBED MRNA POLY(A) TAIL SHORTENING | 67 | -0.43 | -1.31 | 0.149 | 0.831 | 0.977 | 22894 | tags=73%, list=42%, signal=126% | |
675 | NEGATIVE REGULATION OF AUTOPHAGY | 92 | -0.35 | -1.31 | 0.099 | 0.833 | 0.977 | 14903 | tags=45%, list=27%, signal=61% | |
676 | AMYLOID PRECURSOR PROTEIN CATABOLIC PROCESS | 21 | -0.48 | -1.31 | 0.182 | 0.835 | 0.977 | 16531 | tags=67%, list=30%, signal=96% | |
677 | DOLICHOL-LINKED OLIGOSACCHARIDE BIOSYNTHETIC PROCESS | 141 | -0.35 | -1.31 | 0.150 | 0.835 | 0.977 | 19091 | tags=52%, list=35%, signal=79% | |
678 | OLIGOSACCHARIDE-LIPID INTERMEDIATE BIOSYNTHETIC PROCESS | 141 | -0.35 | -1.31 | 0.150 | 0.834 | 0.977 | 19091 | tags=52%, list=35%, signal=79% | |
679 | NEGATIVE REGULATION OF TELOMERE MAINTENANCE VIA TELOMERASE | 47 | -0.40 | -1.31 | 0.097 | 0.833 | 0.977 | 22965 | tags=64%, list=42%, signal=110% | |
680 | ESTABLISHMENT OR MAINTENANCE OF TRANSMEMBRANE ELECTROCHEMICAL GRADIENT | 18 | -0.46 | -1.31 | 0.153 | 0.833 | 0.978 | 16903 | tags=61%, list=31%, signal=88% | |
681 | REGULATION OF G1/S TRANSITION OF MITOTIC CELL CYCLE | 301 | -0.34 | -1.31 | 0.094 | 0.833 | 0.978 | 21276 | tags=56%, list=39%, signal=91% | |
682 | DEOXYRIBONUCLEOSIDE MONOPHOSPHATE BIOSYNTHETIC PROCESS | 9 | -0.55 | -1.31 | 0.132 | 0.833 | 0.978 | 24716 | tags=100%, list=45%, signal=182% | |
683 | PROTEIN DENEDDYLATION | 22 | -0.46 | -1.31 | 0.182 | 0.838 | 0.979 | 23737 | tags=77%, list=43%, signal=137% | |
684 | ENDOTHELIAL TUBE MORPHOGENESIS | 25 | -0.39 | -1.31 | 0.140 | 0.838 | 0.979 | 7688 | tags=32%, list=14%, signal=37% | |
685 | TRANSCRIPTION ELONGATION FROM RNA POLYMERASE III PROMOTER | 39 | -0.42 | -1.31 | 0.155 | 0.838 | 0.980 | 29757 | tags=90%, list=54%, signal=197% | |
686 | TERMINATION OF RNA POLYMERASE III TRANSCRIPTION | 39 | -0.42 | -1.31 | 0.155 | 0.836 | 0.980 | 29757 | tags=90%, list=54%, signal=197% | |
687 | LOCALIZATION WITHIN MEMBRANE | 203 | -0.38 | -1.31 | 0.105 | 0.835 | 0.980 | 25273 | tags=69%, list=46%, signal=129% | |
688 | MULTI-ORGANISM TRANSPORT | 73 | -0.41 | -1.31 | 0.168 | 0.835 | 0.980 | 25447 | tags=75%, list=47%, signal=141% | |
689 | TRANSPORT OF VIRUS | 73 | -0.41 | -1.31 | 0.168 | 0.833 | 0.980 | 25447 | tags=75%, list=47%, signal=141% | |
690 | MULTI-ORGANISM LOCALIZATION | 73 | -0.41 | -1.31 | 0.168 | 0.832 | 0.980 | 25447 | tags=75%, list=47%, signal=141% | |
691 | NEGATIVE REGULATION OF PROTEIN CATABOLIC PROCESS | 281 | -0.36 | -1.31 | 0.090 | 0.833 | 0.980 | 17547 | tags=50%, list=32%, signal=74% | |
692 | NEGATIVE REGULATION OF PROTEASOMAL PROTEIN CATABOLIC PROCESS | 150 | -0.38 | -1.30 | 0.131 | 0.833 | 0.980 | 17763 | tags=53%, list=32%, signal=79% | |
693 | HEXOSE TRANSPORT | 134 | -0.32 | -1.30 | 0.032 | 0.836 | 0.981 | 14921 | tags=38%, list=27%, signal=52% | |
694 | GLUCOSE TRANSPORT | 134 | -0.32 | -1.30 | 0.032 | 0.834 | 0.981 | 14921 | tags=38%, list=27%, signal=52% | |
695 | NEGATIVE REGULATION OF GLUCONEOGENESIS | 16 | -0.44 | -1.30 | 0.152 | 0.837 | 0.982 | 15683 | tags=50%, list=29%, signal=70% | |
696 | ORGANIC CYCLIC COMPOUND CATABOLIC PROCESS | 827 | -0.35 | -1.30 | 0.150 | 0.838 | 0.982 | 22621 | tags=60%, list=41%, signal=101% | |
697 | REGULATION OF ACETYL-COA BIOSYNTHETIC PROCESS FROM PYRUVATE | 30 | -0.46 | -1.30 | 0.202 | 0.837 | 0.982 | 22946 | tags=77%, list=42%, signal=132% | |
698 | REGULATION OF ACYL-COA BIOSYNTHETIC PROCESS | 30 | -0.46 | -1.30 | 0.202 | 0.836 | 0.982 | 22946 | tags=77%, list=42%, signal=132% | |
699 | CHAPERONE-MEDIATED PROTEIN COMPLEX ASSEMBLY | 28 | -0.45 | -1.30 | 0.211 | 0.836 | 0.982 | 21516 | tags=71%, list=39%, signal=118% | |
700 | NEGATIVE REGULATION OF EXECUTION PHASE OF APOPTOSIS | 30 | -0.39 | -1.30 | 0.109 | 0.836 | 0.982 | 10719 | tags=40%, list=20%, signal=50% | |
701 | MITOCHONDRIAL CALCIUM ION TRANSPORT | 12 | -0.48 | -1.30 | 0.154 | 0.838 | 0.982 | 25534 | tags=83%, list=47%, signal=156% | |
702 | MITOCHONDRIAL RNA PROCESSING | 27 | -0.48 | -1.30 | 0.138 | 0.838 | 0.982 | 27355 | tags=93%, list=50%, signal=185% | |
703 | TRICARBOXYLIC ACID METABOLIC PROCESS | 70 | -0.42 | -1.30 | 0.179 | 0.837 | 0.982 | 23125 | tags=73%, list=42%, signal=126% | |
704 | REGULATION OF CANONICAL WNT SIGNALING PATHWAY | 451 | -0.32 | -1.30 | 0.110 | 0.836 | 0.982 | 20764 | tags=51%, list=38%, signal=82% | |
705 | NEGATIVE REGULATION OF AMYLOID PRECURSOR PROTEIN CATABOLIC PROCESS | 21 | -0.45 | -1.30 | 0.198 | 0.835 | 0.982 | 14157 | tags=52%, list=26%, signal=71% | |
706 | REGULATION OF EXIT FROM MITOSIS | 17 | -0.46 | -1.30 | 0.150 | 0.834 | 0.982 | 14434 | tags=59%, list=26%, signal=80% | |
707 | CARBOHYDRATE TRANSPORT | 154 | -0.32 | -1.30 | 0.043 | 0.833 | 0.982 | 14921 | tags=38%, list=27%, signal=53% | |
708 | COFACTOR BIOSYNTHETIC PROCESS | 207 | -0.36 | -1.30 | 0.098 | 0.833 | 0.982 | 20310 | tags=57%, list=37%, signal=91% | |
709 | REGULATION OF RETROGRADE PROTEIN TRANSPORT, ER TO CYTOSOL | 30 | -0.44 | -1.30 | 0.126 | 0.832 | 0.983 | 15093 | tags=57%, list=28%, signal=78% | |
710 | INTRACELLULAR PROTEIN TRANSPORT | 1076 | -0.36 | -1.30 | 0.101 | 0.831 | 0.983 | 21013 | tags=59%, list=38%, signal=93% | |
711 | PREASSEMBLY OF GPI ANCHOR IN ER MEMBRANE | 36 | -0.42 | -1.30 | 0.159 | 0.831 | 0.983 | 21713 | tags=69%, list=40%, signal=115% | |
712 | PROTEIN REPAIR | 16 | -0.47 | -1.30 | 0.184 | 0.832 | 0.983 | 19713 | tags=63%, list=36%, signal=98% | |
713 | TRNA SPLICING, VIA ENDONUCLEOLYTIC CLEAVAGE AND LIGATION | 11 | -0.50 | -1.30 | 0.165 | 0.831 | 0.983 | 20921 | tags=73%, list=38%, signal=118% | |
714 | MITRAL VALVE MORPHOGENESIS | 14 | -0.46 | -1.30 | 0.180 | 0.830 | 0.983 | 12785 | tags=50%, list=23%, signal=65% | |
715 | UBIQUITIN-INDEPENDENT PROTEIN CATABOLIC PROCESS VIA THE MULTIVESICULAR BODY SORTING PATHWAY | 7 | -0.59 | -1.30 | 0.174 | 0.831 | 0.983 | 18914 | tags=86%, list=35%, signal=131% | |
716 | MODIFICATION-DEPENDENT PROTEIN CATABOLIC PROCESS | 727 | -0.37 | -1.30 | 0.117 | 0.830 | 0.983 | 20833 | tags=59%, list=38%, signal=94% | |
717 | VERY LONG-CHAIN FATTY ACID BIOSYNTHETIC PROCESS | 13 | -0.50 | -1.30 | 0.163 | 0.829 | 0.983 | 19619 | tags=69%, list=36%, signal=108% | |
718 | INNATE IMMUNE RESPONSE ACTIVATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 291 | -0.37 | -1.30 | 0.110 | 0.829 | 0.983 | 20868 | tags=58%, list=38%, signal=94% | |
719 | CYTOKINESIS | 188 | -0.35 | -1.30 | 0.071 | 0.829 | 0.983 | 26128 | tags=69%, list=48%, signal=131% | |
720 | CDP-CHOLINE PATHWAY | 14 | -0.52 | -1.30 | 0.162 | 0.828 | 0.983 | 20500 | tags=86%, list=37%, signal=137% | |
721 | NEGATIVE REGULATION OF CATABOLIC PROCESS | 439 | -0.34 | -1.30 | 0.052 | 0.828 | 0.983 | 17233 | tags=47%, list=32%, signal=68% | |
722 | REGULATION OF CELLULAR RESPONSE TO HYPOXIA | 12 | -0.52 | -1.30 | 0.157 | 0.827 | 0.983 | 15733 | tags=75%, list=29%, signal=105% | |
723 | REGULATION OF PROTEIN LOCALIZATION TO CHROMOSOME, TELOMERIC REGION | 42 | -0.43 | -1.30 | 0.106 | 0.827 | 0.983 | 25955 | tags=81%, list=47%, signal=154% | |
724 | NEGATIVE REGULATION OF MITOTIC CELL CYCLE PHASE TRANSITION | 352 | -0.37 | -1.30 | 0.120 | 0.826 | 0.983 | 20654 | tags=59%, list=38%, signal=94% | |
725 | RNA PHOSPHODIESTER BOND HYDROLYSIS | 134 | -0.38 | -1.30 | 0.050 | 0.826 | 0.983 | 23584 | tags=67%, list=43%, signal=118% | |
726 | PROTEIN EXIT FROM ENDOPLASMIC RETICULUM | 40 | -0.41 | -1.30 | 0.222 | 0.825 | 0.983 | 15730 | tags=55%, list=29%, signal=77% | |
727 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO CHROMOSOME | 21 | -0.51 | -1.30 | 0.207 | 0.824 | 0.983 | 25365 | tags=90%, list=46%, signal=169% | |
728 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO TELOMERE | 21 | -0.51 | -1.30 | 0.207 | 0.823 | 0.983 | 25365 | tags=90%, list=46%, signal=169% | |
729 | NUCLEOSIDE PHOSPHATE METABOLIC PROCESS | 634 | -0.32 | -1.30 | 0.072 | 0.822 | 0.983 | 21242 | tags=53%, list=39%, signal=85% | |
730 | EPITHELIAL CELL FATE COMMITMENT | 21 | -0.42 | -1.30 | 0.144 | 0.822 | 0.983 | 24501 | tags=71%, list=45%, signal=129% | |
731 | ERROR-FREE TRANSLESION SYNTHESIS | 39 | -0.44 | -1.30 | 0.172 | 0.822 | 0.983 | 17205 | tags=64%, list=31%, signal=93% | |
732 | POSITIVE REGULATION OF DNA-TEMPLATED TRANSCRIPTION, ELONGATION | 46 | -0.42 | -1.30 | 0.070 | 0.821 | 0.983 | 15797 | tags=57%, list=29%, signal=79% | |
733 | VESICLE TARGETING, ROUGH ER TO CIS-GOLGI | 151 | -0.37 | -1.30 | 0.129 | 0.822 | 0.983 | 25273 | tags=68%, list=46%, signal=126% | |
734 | COPII VESICLE COATING | 151 | -0.37 | -1.30 | 0.129 | 0.821 | 0.983 | 25273 | tags=68%, list=46%, signal=126% | |
735 | UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 722 | -0.37 | -1.30 | 0.119 | 0.820 | 0.983 | 20833 | tags=59%, list=38%, signal=93% | |
736 | RESPONSE TO DSRNA | 92 | -0.37 | -1.30 | 0.081 | 0.820 | 0.983 | 15754 | tags=49%, list=29%, signal=69% | |
737 | NUCLEOBASE METABOLIC PROCESS | 124 | -0.36 | -1.30 | 0.098 | 0.820 | 0.983 | 28039 | tags=76%, list=51%, signal=155% | |
738 | ORGANOPHOSPHATE CATABOLIC PROCESS | 166 | -0.34 | -1.30 | 0.028 | 0.819 | 0.983 | 18246 | tags=48%, list=33%, signal=72% | |
739 | RELEASE OF SEQUESTERED CALCIUM ION INTO CYTOSOL BY SARCOPLASMIC RETICULUM | 12 | -0.48 | -1.30 | 0.171 | 0.820 | 0.984 | 1143 | tags=25%, list=2%, signal=26% | |
740 | CALCIUM ION TRANSPORT FROM ENDOPLASMIC RETICULUM TO CYTOSOL | 12 | -0.48 | -1.30 | 0.171 | 0.818 | 0.984 | 1143 | tags=25%, list=2%, signal=26% | |
741 | REGULATION OF PROTEIN STABILITY | 462 | -0.35 | -1.29 | 0.068 | 0.819 | 0.984 | 21501 | tags=58%, list=39%, signal=95% | |
742 | POSITIVE REGULATION OF PROTEIN HOMODIMERIZATION ACTIVITY | 19 | -0.44 | -1.29 | 0.163 | 0.819 | 0.984 | 8883 | tags=42%, list=16%, signal=50% | |
743 | NEGATIVE REGULATION OF ENDOPLASMIC RETICULUM CALCIUM ION CONCENTRATION | 13 | -0.48 | -1.29 | 0.163 | 0.818 | 0.984 | 8238 | tags=46%, list=15%, signal=54% | |
744 | RESPONSE TO STIMULUS INVOLVED IN REGULATION OF MUSCLE ADAPTATION | 15 | -0.44 | -1.29 | 0.144 | 0.817 | 0.984 | 6383 | tags=33%, list=12%, signal=38% | |
745 | CHROMOSOME LOCALIZATION | 81 | -0.39 | -1.29 | 0.172 | 0.816 | 0.984 | 21773 | tags=64%, list=40%, signal=107% | |
746 | ESTABLISHMENT OF CHROMOSOME LOCALIZATION | 81 | -0.39 | -1.29 | 0.172 | 0.815 | 0.984 | 21773 | tags=64%, list=40%, signal=107% | |
747 | NEGATIVE REGULATION OF CALCIUM ION IMPORT | 37 | -0.39 | -1.29 | 0.159 | 0.817 | 0.984 | 19515 | tags=54%, list=36%, signal=84% | |
748 | CELLULAR LIPID CATABOLIC PROCESS | 223 | -0.33 | -1.29 | 0.116 | 0.816 | 0.984 | 26237 | tags=64%, list=48%, signal=123% | |
749 | INTRACELLULAR TRANSPORT OF VIRUS | 66 | -0.42 | -1.29 | 0.144 | 0.815 | 0.984 | 25447 | tags=77%, list=47%, signal=144% | |
750 | MULTI-ORGANISM INTRACELLULAR TRANSPORT | 66 | -0.42 | -1.29 | 0.144 | 0.814 | 0.984 | 25447 | tags=77%, list=47%, signal=144% | |
751 | REGULATION OF EPIDERMAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 170 | -0.34 | -1.29 | 0.084 | 0.814 | 0.984 | 15001 | tags=42%, list=27%, signal=58% | |
752 | GALACTOSE METABOLIC PROCESS | 19 | -0.45 | -1.29 | 0.166 | 0.815 | 0.984 | 29695 | tags=95%, list=54%, signal=207% | |
753 | TRANSCRIPTION-COUPLED NUCLEOTIDE-EXCISION REPAIR | 148 | -0.40 | -1.29 | 0.144 | 0.814 | 0.984 | 18814 | tags=60%, list=34%, signal=91% | |
754 | ACTIVATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC PROCESS BY CYTOCHROME C | 13 | -0.50 | -1.29 | 0.181 | 0.815 | 0.985 | 13407 | tags=62%, list=25%, signal=82% | |
755 | VESICLE TRANSPORT ALONG MICROTUBULE | 59 | -0.41 | -1.29 | 0.168 | 0.814 | 0.985 | 18135 | tags=59%, list=33%, signal=89% | |
756 | REGULATION OF PROTEIN CATABOLIC PROCESS | 743 | -0.36 | -1.29 | 0.095 | 0.814 | 0.985 | 20632 | tags=56%, list=38%, signal=89% | |
757 | NEGATIVE REGULATION OF PROTEIN BINDING | 148 | -0.34 | -1.29 | 0.086 | 0.814 | 0.985 | 16315 | tags=45%, list=30%, signal=64% | |
758 | MEMBRANE PROTEIN INTRACELLULAR DOMAIN PROTEOLYSIS | 37 | -0.41 | -1.29 | 0.211 | 0.814 | 0.985 | 25181 | tags=73%, list=46%, signal=135% | |
759 | POSITIVE REGULATION OF HISTONE H3-K9 METHYLATION | 8 | -0.53 | -1.29 | 0.150 | 0.814 | 0.985 | 11026 | tags=50%, list=20%, signal=63% | |
760 | PHOSPHATIDYLETHANOLAMINE ACYL-CHAIN REMODELING | 42 | -0.37 | -1.29 | 0.139 | 0.816 | 0.985 | 23706 | tags=64%, list=43%, signal=113% | |
761 | NEGATIVE REGULATION OF WNT SIGNALING PATHWAY | 367 | -0.32 | -1.29 | 0.137 | 0.815 | 0.985 | 20764 | tags=51%, list=38%, signal=82% | |
762 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO CHROMOSOME, TELOMERIC REGION | 35 | -0.43 | -1.29 | 0.124 | 0.814 | 0.985 | 25955 | tags=80%, list=47%, signal=152% | |
763 | ESTABLISHMENT OF INTEGRATED PROVIRAL LATENCY | 26 | -0.45 | -1.29 | 0.156 | 0.813 | 0.985 | 16208 | tags=54%, list=30%, signal=76% | |
764 | PIRNA METABOLIC PROCESS | 48 | -0.38 | -1.29 | 0.164 | 0.813 | 0.985 | 24155 | tags=65%, list=44%, signal=116% | |
765 | MODIFICATION-DEPENDENT MACROMOLECULE CATABOLIC PROCESS | 735 | -0.37 | -1.29 | 0.117 | 0.815 | 0.986 | 20833 | tags=59%, list=38%, signal=93% | |
766 | PROTEIN STABILIZATION | 306 | -0.36 | -1.29 | 0.041 | 0.815 | 0.986 | 21070 | tags=59%, list=39%, signal=95% | |
767 | CELLULAR RESPONSE TO HYPOXIA | 231 | -0.33 | -1.29 | 0.059 | 0.816 | 0.986 | 23179 | tags=56%, list=42%, signal=97% | |
768 | DNA-TEMPLATED TRANSCRIPTION, ELONGATION | 209 | -0.38 | -1.29 | 0.127 | 0.815 | 0.986 | 28016 | tags=78%, list=51%, signal=158% | |
769 | N-ACETYLNEURAMINATE METABOLIC PROCESS | 16 | -0.44 | -1.29 | 0.184 | 0.814 | 0.986 | 11451 | tags=50%, list=21%, signal=63% | |
770 | REGULATION OF CAMP-DEPENDENT PROTEIN KINASE ACTIVITY | 24 | -0.43 | -1.29 | 0.190 | 0.813 | 0.986 | 21608 | tags=67%, list=40%, signal=110% | |
771 | CELLULAR COMPONENT DISASSEMBLY INVOLVED IN EXECUTION PHASE OF APOPTOSIS | 145 | -0.35 | -1.29 | 0.132 | 0.816 | 0.986 | 17224 | tags=50%, list=32%, signal=72% | |
772 | COENZYME A METABOLIC PROCESS | 13 | -0.48 | -1.29 | 0.162 | 0.816 | 0.986 | 21408 | tags=77%, list=39%, signal=126% | |
773 | RIBOSE PHOSPHATE BIOSYNTHETIC PROCESS | 162 | -0.33 | -1.29 | 0.184 | 0.815 | 0.986 | 21088 | tags=52%, list=39%, signal=84% | |
774 | LAMELLIPODIUM ORGANIZATION | 70 | -0.38 | -1.29 | 0.117 | 0.814 | 0.986 | 14877 | tags=46%, list=27%, signal=63% | |
775 | POSITIVE REGULATION OF VACUOLE ORGANIZATION | 32 | -0.44 | -1.29 | 0.113 | 0.816 | 0.986 | 27620 | tags=91%, list=51%, signal=183% | |
776 | SPINDLE LOCALIZATION | 59 | -0.37 | -1.29 | 0.148 | 0.816 | 0.986 | 26797 | tags=69%, list=49%, signal=136% | |
777 | VESICLE COATING | 200 | -0.37 | -1.29 | 0.109 | 0.815 | 0.986 | 25281 | tags=68%, list=46%, signal=126% | |
778 | PROTEASOMAL PROTEIN CATABOLIC PROCESS | 531 | -0.37 | -1.29 | 0.131 | 0.816 | 0.986 | 19263 | tags=56%, list=35%, signal=86% | |
779 | NEGATIVE REGULATION OF PROTEASOMAL UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 143 | -0.38 | -1.29 | 0.154 | 0.816 | 0.986 | 17763 | tags=53%, list=32%, signal=79% | |
780 | POSITIVE REGULATION OF NEUTROPHIL CHEMOTAXIS | 29 | -0.43 | -1.29 | 0.191 | 0.818 | 0.986 | 19058 | tags=55%, list=35%, signal=85% | |
781 | VESICLE ORGANIZATION | 366 | -0.37 | -1.29 | 0.099 | 0.818 | 0.986 | 24678 | tags=66%, list=45%, signal=119% | |
782 | PRIMARY MIRNA PROCESSING | 30 | -0.41 | -1.28 | 0.172 | 0.818 | 0.986 | 21517 | tags=63%, list=39%, signal=104% | |
783 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 105 | -0.36 | -1.28 | 0.103 | 0.819 | 0.986 | 12304 | tags=43%, list=23%, signal=55% | |
784 | IRON ION HOMEOSTASIS | 161 | -0.34 | -1.28 | 0.074 | 0.821 | 0.986 | 17911 | tags=48%, list=33%, signal=72% | |
785 | SOMATIC STEM CELL POPULATION MAINTENANCE | 84 | -0.34 | -1.28 | 0.149 | 0.820 | 0.986 | 19109 | tags=46%, list=35%, signal=71% | |
786 | GLYCOGEN METABOLIC PROCESS | 78 | -0.37 | -1.28 | 0.132 | 0.820 | 0.986 | 19941 | tags=54%, list=36%, signal=85% | |
787 | RNA MODIFICATION | 142 | -0.36 | -1.28 | 0.178 | 0.819 | 0.986 | 22121 | tags=61%, list=40%, signal=103% | |
788 | GOLGI TO ENDOSOME TRANSPORT | 30 | -0.46 | -1.28 | 0.236 | 0.822 | 0.986 | 21442 | tags=77%, list=39%, signal=126% | |
789 | ER-ASSOCIATED UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 112 | -0.40 | -1.28 | 0.197 | 0.821 | 0.986 | 16961 | tags=55%, list=31%, signal=80% | |
790 | COPII-COATED VESICLE BUDDING | 161 | -0.37 | -1.28 | 0.146 | 0.821 | 0.986 | 25273 | tags=68%, list=46%, signal=126% | |
791 | NEGATIVE REGULATION OF HISTONE METHYLATION | 30 | -0.43 | -1.28 | 0.141 | 0.821 | 0.986 | 15303 | tags=57%, list=28%, signal=79% | |
792 | CELLULAR RESPONSE TO CORTICOSTEROID STIMULUS | 22 | -0.43 | -1.28 | 0.165 | 0.820 | 0.986 | 20883 | tags=64%, list=38%, signal=103% | |
793 | INTRA-GOLGI VESICLE-MEDIATED TRANSPORT | 35 | -0.43 | -1.28 | 0.139 | 0.819 | 0.986 | 22137 | tags=69%, list=40%, signal=115% | |
794 | BASE-EXCISION REPAIR | 90 | -0.36 | -1.28 | 0.134 | 0.818 | 0.986 | 19793 | tags=56%, list=36%, signal=87% | |
795 | COLLAGEN-ACTIVATED SIGNALING PATHWAY | 12 | -0.47 | -1.28 | 0.160 | 0.818 | 0.986 | 10446 | tags=42%, list=19%, signal=51% | |
796 | NUCLEOBASE-CONTAINING SMALL MOLECULE METABOLIC PROCESS | 738 | -0.32 | -1.28 | 0.075 | 0.818 | 0.986 | 21482 | tags=53%, list=39%, signal=87% | |
797 | POSITIVE REGULATION OF WNT SIGNALING PATHWAY | 337 | -0.34 | -1.28 | 0.119 | 0.819 | 0.986 | 19835 | tags=51%, list=36%, signal=80% | |
798 | NUCLEOTIDE METABOLIC PROCESS | 605 | -0.32 | -1.28 | 0.079 | 0.819 | 0.986 | 21242 | tags=52%, list=39%, signal=84% | |
799 | REGULATION OF AMYLOID PRECURSOR PROTEIN BIOSYNTHETIC PROCESS | 10 | -0.53 | -1.28 | 0.146 | 0.824 | 0.986 | 17659 | tags=80%, list=32%, signal=118% | |
800 | REGULATION OF CELL CYCLE G1/S PHASE TRANSITION | 327 | -0.33 | -1.28 | 0.111 | 0.823 | 0.986 | 25186 | tags=62%, list=46%, signal=115% | |
801 | NEGATIVE REGULATION OF CELL CYCLE PHASE TRANSITION | 376 | -0.36 | -1.28 | 0.118 | 0.822 | 0.986 | 20654 | tags=57%, list=38%, signal=92% | |
802 | NUCLEIC ACID PHOSPHODIESTER BOND HYDROLYSIS | 348 | -0.37 | -1.28 | 0.104 | 0.821 | 0.986 | 20458 | tags=59%, list=37%, signal=93% | |
803 | NEGATIVE REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 36 | -0.40 | -1.28 | 0.170 | 0.821 | 0.986 | 19530 | tags=61%, list=36%, signal=95% | |
804 | PROTEIN-LIPID COMPLEX ASSEMBLY | 35 | -0.40 | -1.28 | 0.199 | 0.821 | 0.986 | 24670 | tags=66%, list=45%, signal=120% | |
805 | NUCLEOTIDE BIOSYNTHETIC PROCESS | 194 | -0.33 | -1.28 | 0.159 | 0.822 | 0.986 | 21153 | tags=53%, list=39%, signal=86% | |
806 | PROTEIN LOCALIZATION TO CHROMATIN | 15 | -0.46 | -1.28 | 0.174 | 0.821 | 0.986 | 8761 | tags=47%, list=16%, signal=56% | |
807 | CULLIN DENEDDYLATION | 19 | -0.45 | -1.28 | 0.214 | 0.821 | 0.986 | 23737 | tags=79%, list=43%, signal=139% | |
808 | RIBONUCLEOPROTEIN COMPLEX BIOGENESIS | 419 | -0.37 | -1.28 | 0.110 | 0.821 | 0.986 | 24673 | tags=67%, list=45%, signal=121% | |
809 | PROTEIN CATABOLIC PROCESS | 883 | -0.35 | -1.28 | 0.111 | 0.820 | 0.986 | 20833 | tags=57%, list=38%, signal=90% | |
810 | POSITIVE REGULATION OF TELOMERE MAINTENANCE VIA TELOMERASE | 70 | -0.39 | -1.28 | 0.155 | 0.820 | 0.986 | 23271 | tags=67%, list=43%, signal=117% | |
811 | PURINE NUCLEOSIDE METABOLIC PROCESS | 319 | -0.33 | -1.28 | 0.145 | 0.820 | 0.986 | 20756 | tags=54%, list=38%, signal=87% | |
812 | ISG15-PROTEIN CONJUGATION | 6 | -0.62 | -1.28 | 0.175 | 0.821 | 0.986 | 1556 | tags=50%, list=3%, signal=51% | |
813 | L-SERINE TRANSPORT | 7 | -0.58 | -1.28 | 0.179 | 0.820 | 0.986 | 20980 | tags=86%, list=38%, signal=139% | |
814 | SERINE TRANSPORT | 7 | -0.58 | -1.28 | 0.179 | 0.819 | 0.986 | 20980 | tags=86%, list=38%, signal=139% | |
815 | REGULATION OF ERBB SIGNALING PATHWAY | 174 | -0.34 | -1.28 | 0.095 | 0.818 | 0.986 | 23009 | tags=56%, list=42%, signal=97% | |
816 | MYELIN ASSEMBLY | 16 | -0.44 | -1.28 | 0.148 | 0.819 | 0.986 | 21709 | tags=75%, list=40%, signal=124% | |
817 | REGULATION OF T CELL APOPTOTIC PROCESS | 28 | -0.41 | -1.28 | 0.229 | 0.818 | 0.986 | 6919 | tags=36%, list=13%, signal=41% | |
818 | REGULATION OF PROTEIN PHOSPHATASE TYPE 2A ACTIVITY | 62 | -0.41 | -1.28 | 0.148 | 0.817 | 0.986 | 21835 | tags=69%, list=40%, signal=115% | |
819 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO CHROMATIN | 12 | -0.51 | -1.28 | 0.165 | 0.818 | 0.986 | 7264 | tags=50%, list=13%, signal=58% | |
820 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 49 | -0.38 | -1.28 | 0.155 | 0.818 | 0.986 | 20347 | tags=55%, list=37%, signal=88% | |
821 | REGULATION OF SKELETAL MUSCLE SATELLITE CELL PROLIFERATION | 20 | -0.49 | -1.27 | 0.235 | 0.819 | 0.986 | 18530 | tags=65%, list=34%, signal=98% | |
822 | REGULATION OF SKELETAL MUSCLE CELL PROLIFERATION | 20 | -0.49 | -1.27 | 0.235 | 0.818 | 0.986 | 18530 | tags=65%, list=34%, signal=98% | |
823 | VESICLE CYTOSKELETAL TRAFFICKING | 69 | -0.39 | -1.27 | 0.191 | 0.817 | 0.986 | 18135 | tags=55%, list=33%, signal=82% | |
824 | PURINE DEOXYRIBONUCLEOTIDE METABOLIC PROCESS | 23 | -0.43 | -1.27 | 0.161 | 0.817 | 0.986 | 15508 | tags=52%, list=28%, signal=73% | |
825 | DOLICHYL DIPHOSPHATE BIOSYNTHETIC PROCESS | 11 | -0.52 | -1.27 | 0.200 | 0.816 | 0.986 | 18704 | tags=73%, list=34%, signal=111% | |
826 | DOLICHYL DIPHOSPHATE METABOLIC PROCESS | 11 | -0.52 | -1.27 | 0.200 | 0.815 | 0.986 | 18704 | tags=73%, list=34%, signal=111% | |
827 | NEGATIVE REGULATION OF GENE SILENCING BY MIRNA | 7 | -0.54 | -1.27 | 0.188 | 0.815 | 0.986 | 6172 | tags=43%, list=11%, signal=48% | |
828 | NONRIBOSOMAL PEPTIDE BIOSYNTHETIC PROCESS | 26 | -0.43 | -1.27 | 0.163 | 0.814 | 0.986 | 23642 | tags=77%, list=43%, signal=135% | |
829 | SKELETAL MUSCLE CONTRACTION | 24 | -0.46 | -1.27 | 0.232 | 0.814 | 0.986 | 14748 | tags=46%, list=27%, signal=63% | |
830 | PYRIMIDINE NUCLEOTIDE CATABOLIC PROCESS | 23 | -0.41 | -1.27 | 0.183 | 0.813 | 0.986 | 16304 | tags=52%, list=30%, signal=74% | |
831 | REGULATION OF CELLULAR CATABOLIC PROCESS | 1155 | -0.33 | -1.27 | 0.075 | 0.813 | 0.986 | 19011 | tags=50%, list=35%, signal=75% | |
832 | CELLULAR RESPONSE TO EPIDERMAL GROWTH FACTOR STIMULUS | 48 | -0.38 | -1.27 | 0.192 | 0.812 | 0.986 | 15828 | tags=48%, list=29%, signal=67% | |
833 | 2-OXOGLUTARATE METABOLIC PROCESS | 24 | -0.44 | -1.27 | 0.182 | 0.812 | 0.986 | 24700 | tags=79%, list=45%, signal=144% | |
834 | REGULATION OF TRANSCRIPTION ELONGATION FROM RNA POLYMERASE II PROMOTER | 41 | -0.37 | -1.27 | 0.128 | 0.812 | 0.986 | 15797 | tags=46%, list=29%, signal=65% | |
835 | POSITIVE REGULATION OF TRIGLYCERIDE BIOSYNTHETIC PROCESS | 28 | -0.39 | -1.27 | 0.187 | 0.812 | 0.986 | 16447 | tags=46%, list=30%, signal=66% | |
836 | REGULATION OF DEFENSE RESPONSE TO BACTERIUM | 20 | -0.42 | -1.27 | 0.208 | 0.812 | 0.986 | 19607 | tags=55%, list=36%, signal=86% | |
837 | NUCLEOSIDE PHOSPHATE CATABOLIC PROCESS | 121 | -0.33 | -1.27 | 0.050 | 0.812 | 0.986 | 16617 | tags=44%, list=30%, signal=63% | |
838 | ACROSOME REACTION | 9 | -0.51 | -1.27 | 0.183 | 0.811 | 0.986 | 9560 | tags=44%, list=17%, signal=54% | |
839 | CELLULAR RESPONSE TO DECREASED OXYGEN LEVELS | 237 | -0.33 | -1.27 | 0.073 | 0.810 | 0.986 | 23179 | tags=56%, list=42%, signal=96% | |
840 | HISTONE MONOUBIQUITINATION | 48 | -0.42 | -1.27 | 0.193 | 0.810 | 0.986 | 23276 | tags=73%, list=43%, signal=127% | |
841 | REGULATION OF TELOMERASE RNA LOCALIZATION TO CAJAL BODY | 27 | -0.49 | -1.27 | 0.231 | 0.809 | 0.986 | 15273 | tags=67%, list=28%, signal=92% | |
842 | POSITIVE REGULATION OF TELOMERASE RNA LOCALIZATION TO CAJAL BODY | 27 | -0.49 | -1.27 | 0.231 | 0.808 | 0.986 | 15273 | tags=67%, list=28%, signal=92% | |
843 | PROTEIN LOCALIZATION TO ORGANELLE | 1087 | -0.36 | -1.27 | 0.107 | 0.808 | 0.986 | 22451 | tags=61%, list=41%, signal=101% | |
844 | POSITIVE REGULATION OF SEQUESTERING OF CALCIUM ION | 26 | -0.41 | -1.27 | 0.186 | 0.807 | 0.986 | 19515 | tags=58%, list=36%, signal=90% | |
845 | PROTEOLYSIS INVOLVED IN CELLULAR PROTEIN CATABOLIC PROCESS | 798 | -0.36 | -1.27 | 0.139 | 0.807 | 0.986 | 22471 | tags=61%, list=41%, signal=101% | |
846 | REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 127 | -0.33 | -1.27 | 0.175 | 0.809 | 0.986 | 7829 | tags=27%, list=14%, signal=31% | |
847 | PURINE NUCLEOBASE METABOLIC PROCESS | 78 | -0.38 | -1.27 | 0.126 | 0.808 | 0.986 | 26466 | tags=74%, list=48%, signal=144% | |
848 | SHORT-CHAIN FATTY ACID METABOLIC PROCESS | 19 | -0.47 | -1.27 | 0.237 | 0.807 | 0.986 | 22394 | tags=74%, list=41%, signal=125% | |
849 | REGULATION OF IMMUNOGLOBULIN MEDIATED IMMUNE RESPONSE | 37 | -0.42 | -1.27 | 0.176 | 0.809 | 0.986 | 5307 | tags=32%, list=10%, signal=36% | |
850 | ER TO GOLGI VESICLE-MEDIATED TRANSPORT | 365 | -0.34 | -1.27 | 0.110 | 0.809 | 0.986 | 25853 | tags=64%, list=47%, signal=120% | |
851 | NEGATIVE REGULATION OF CELL DIVISION | 149 | -0.36 | -1.27 | 0.153 | 0.808 | 0.986 | 17763 | tags=52%, list=32%, signal=76% | |
852 | PROTEIN N-LINKED GLYCOSYLATION | 596 | -0.33 | -1.27 | 0.108 | 0.809 | 0.987 | 21509 | tags=55%, list=39%, signal=89% | |
853 | REGULATION OF PROTEIN SUMOYLATION | 33 | -0.40 | -1.27 | 0.175 | 0.808 | 0.987 | 6078 | tags=33%, list=11%, signal=37% | |
854 | PURINE RIBONUCLEOTIDE TRANSPORT | 10 | -0.48 | -1.27 | 0.180 | 0.809 | 0.987 | 9403 | tags=40%, list=17%, signal=48% | |
855 | ADENINE NUCLEOTIDE TRANSPORT | 10 | -0.48 | -1.27 | 0.180 | 0.808 | 0.987 | 9403 | tags=40%, list=17%, signal=48% | |
856 | HISTONE H4 DEACETYLATION | 18 | -0.41 | -1.27 | 0.159 | 0.807 | 0.987 | 12052 | tags=44%, list=22%, signal=57% | |
857 | REGULATION OF DEVELOPMENTAL PIGMENTATION | 16 | -0.48 | -1.27 | 0.200 | 0.807 | 0.987 | 12706 | tags=50%, list=23%, signal=65% | |
858 | FATTY ACID ELONGATION, SATURATED FATTY ACID | 8 | -0.53 | -1.27 | 0.179 | 0.808 | 0.987 | 9042 | tags=50%, list=17%, signal=60% | |
859 | CELLULAR GLUCAN METABOLIC PROCESS | 79 | -0.36 | -1.27 | 0.133 | 0.808 | 0.988 | 19941 | tags=53%, list=36%, signal=84% | |
860 | GLUCAN METABOLIC PROCESS | 79 | -0.36 | -1.27 | 0.133 | 0.807 | 0.988 | 19941 | tags=53%, list=36%, signal=84% | |
861 | POSITIVE REGULATION OF MACROPHAGE DIFFERENTIATION | 22 | -0.40 | -1.27 | 0.165 | 0.806 | 0.988 | 8905 | tags=27%, list=16%, signal=33% | |
862 | INTERSTRAND CROSS-LINK REPAIR | 73 | -0.36 | -1.27 | 0.079 | 0.810 | 0.988 | 14973 | tags=45%, list=27%, signal=62% | |
863 | TRANSCRIPTION ELONGATION FROM RNA POLYMERASE II PROMOTER | 147 | -0.38 | -1.27 | 0.195 | 0.810 | 0.988 | 27793 | tags=78%, list=51%, signal=159% | |
864 | PEPTIDYL-ASPARAGINE MODIFICATION | 583 | -0.33 | -1.27 | 0.105 | 0.810 | 0.988 | 21164 | tags=54%, list=39%, signal=87% | |
865 | GLOBAL GENOME NUCLEOTIDE-EXCISION REPAIR | 125 | -0.40 | -1.27 | 0.201 | 0.811 | 0.988 | 20790 | tags=66%, list=38%, signal=106% | |
866 | PHOSPHATIDYLCHOLINE METABOLIC PROCESS | 115 | -0.32 | -1.27 | 0.127 | 0.810 | 0.988 | 24425 | tags=58%, list=45%, signal=105% | |
867 | TRNA PROCESSING | 221 | -0.37 | -1.27 | 0.195 | 0.809 | 0.988 | 22639 | tags=63%, list=41%, signal=107% | |
868 | PURINE RIBONUCLEOSIDE METABOLIC PROCESS | 311 | -0.33 | -1.27 | 0.168 | 0.810 | 0.988 | 20756 | tags=54%, list=38%, signal=86% | |
869 | MITRAL VALVE DEVELOPMENT | 16 | -0.44 | -1.27 | 0.201 | 0.810 | 0.988 | 12785 | tags=44%, list=23%, signal=57% | |
870 | POSITIVE REGULATION OF TELOMERE MAINTENANCE VIA TELOMERE LENGTHENING | 74 | -0.37 | -1.27 | 0.168 | 0.810 | 0.988 | 23271 | tags=64%, list=43%, signal=110% | |
871 | REGULATION OF MEIOTIC NUCLEAR DIVISION | 15 | -0.47 | -1.27 | 0.193 | 0.809 | 0.988 | 5252 | tags=40%, list=10%, signal=44% | |
872 | SMALL MOLECULE CATABOLIC PROCESS | 498 | -0.31 | -1.27 | 0.124 | 0.808 | 0.988 | 20303 | tags=49%, list=37%, signal=78% | |
873 | BONE CELL DEVELOPMENT | 19 | -0.48 | -1.27 | 0.162 | 0.808 | 0.988 | 19607 | tags=74%, list=36%, signal=115% | |
874 | CELLULAR PROTEIN CATABOLIC PROCESS | 829 | -0.35 | -1.27 | 0.129 | 0.808 | 0.988 | 22471 | tags=60%, list=41%, signal=100% | |
875 | REGULATION OF PROTEIN LOCALIZATION TO CELL SURFACE | 57 | -0.36 | -1.26 | 0.144 | 0.810 | 0.988 | 8429 | tags=35%, list=15%, signal=41% | |
876 | PROTEIN N-LINKED GLYCOSYLATION VIA ASPARAGINE | 580 | -0.33 | -1.26 | 0.106 | 0.809 | 0.988 | 21164 | tags=54%, list=39%, signal=87% | |
877 | POSITIVE REGULATION OF VIRAL RELEASE FROM HOST CELL | 29 | -0.45 | -1.26 | 0.223 | 0.809 | 0.988 | 20245 | tags=69%, list=37%, signal=109% | |
878 | POSITIVE REGULATION OF TELOMERASE ACTIVITY | 59 | -0.39 | -1.26 | 0.196 | 0.810 | 0.988 | 23219 | tags=68%, list=42%, signal=118% | |
879 | ANTIGEN PROCESSING AND PRESENTATION OF ENDOGENOUS PEPTIDE ANTIGEN VIA MHC CLASS I | 27 | -0.45 | -1.26 | 0.229 | 0.810 | 0.988 | 14736 | tags=52%, list=27%, signal=71% | |
880 | POSITIVE REGULATION OF DELAYED RECTIFIER POTASSIUM CHANNEL ACTIVITY | 13 | -0.44 | -1.26 | 0.185 | 0.809 | 0.988 | 15329 | tags=46%, list=28%, signal=64% | |
881 | POSITIVE REGULATION OF VOLTAGE-GATED POTASSIUM CHANNEL ACTIVITY | 13 | -0.44 | -1.26 | 0.185 | 0.808 | 0.988 | 15329 | tags=46%, list=28%, signal=64% | |
882 | GLAND MORPHOGENESIS | 39 | -0.39 | -1.26 | 0.193 | 0.809 | 0.988 | 15881 | tags=46%, list=29%, signal=65% | |
883 | NEGATIVE REGULATION OF TELOMERE MAINTENANCE VIA TELOMERE LENGTHENING | 57 | -0.37 | -1.26 | 0.179 | 0.808 | 0.988 | 22965 | tags=60%, list=42%, signal=103% | |
884 | REGULATION OF TYPE B PANCREATIC CELL APOPTOTIC PROCESS | 17 | -0.47 | -1.26 | 0.165 | 0.808 | 0.988 | 24905 | tags=82%, list=46%, signal=151% | |
885 | RNA PROCESSING | 1188 | -0.36 | -1.26 | 0.162 | 0.807 | 0.988 | 23808 | tags=63%, list=44%, signal=109% | |
886 | COFACTOR METABOLIC PROCESS | 498 | -0.32 | -1.26 | 0.112 | 0.808 | 0.988 | 20310 | tags=50%, list=37%, signal=79% | |
887 | GOLGI RIBBON FORMATION | 36 | -0.40 | -1.26 | 0.223 | 0.810 | 0.988 | 17602 | tags=56%, list=32%, signal=82% | |
888 | DICARBOXYLIC ACID METABOLIC PROCESS | 132 | -0.35 | -1.26 | 0.058 | 0.811 | 0.988 | 25424 | tags=64%, list=47%, signal=120% | |
889 | CELLULAR RESPONSE TO DSRNA | 82 | -0.36 | -1.26 | 0.140 | 0.811 | 0.988 | 17146 | tags=50%, list=31%, signal=73% | |
890 | NUCLEOSIDE METABOLIC PROCESS | 399 | -0.32 | -1.26 | 0.152 | 0.810 | 0.988 | 21408 | tags=55%, list=39%, signal=90% | |
891 | SYNAPTIC VESICLE LOCALIZATION | 105 | -0.34 | -1.26 | 0.107 | 0.810 | 0.988 | 16426 | tags=43%, list=30%, signal=61% | |
892 | PROTEIN LOCALIZATION TO MICROTUBULE | 17 | -0.48 | -1.26 | 0.200 | 0.809 | 0.988 | 18314 | tags=71%, list=33%, signal=106% | |
893 | REGULATION OF ANTIGEN PROCESSING AND PRESENTATION OF PEPTIDE ANTIGEN | 26 | -0.42 | -1.26 | 0.211 | 0.808 | 0.988 | 3999 | tags=27%, list=7%, signal=29% | |
894 | POSITIVE REGULATION OF CATABOLIC PROCESS | 754 | -0.34 | -1.26 | 0.102 | 0.808 | 0.989 | 20632 | tags=55%, list=38%, signal=87% | |
895 | RNA SPLICING, VIA ENDONUCLEOLYTIC CLEAVAGE AND LIGATION | 13 | -0.47 | -1.26 | 0.160 | 0.808 | 0.989 | 20921 | tags=69%, list=38%, signal=112% | |
896 | ESTABLISHMENT OF ORGANELLE LOCALIZATION | 527 | -0.35 | -1.26 | 0.122 | 0.808 | 0.989 | 24834 | tags=64%, list=45%, signal=115% | |
897 | POSITIVE REGULATION OF CELLULAR CATABOLIC PROCESS | 661 | -0.34 | -1.26 | 0.109 | 0.807 | 0.989 | 20632 | tags=56%, list=38%, signal=88% | |
898 | MONOSACCHARIDE METABOLIC PROCESS | 267 | -0.33 | -1.26 | 0.187 | 0.806 | 0.989 | 27861 | tags=67%, list=51%, signal=137% | |
899 | NEGATIVE REGULATION OF MRNA 3'-END PROCESSING | 13 | -0.47 | -1.26 | 0.185 | 0.806 | 0.989 | 19323 | tags=62%, list=35%, signal=95% | |
900 | ANTIGEN PROCESSING AND PRESENTATION OF EXOGENOUS PEPTIDE ANTIGEN | 370 | -0.35 | -1.26 | 0.188 | 0.806 | 0.989 | 25887 | tags=67%, list=47%, signal=126% | |
901 | ANTIGEN PROCESSING AND PRESENTATION OF EXOGENOUS ANTIGEN | 370 | -0.35 | -1.26 | 0.188 | 0.805 | 0.989 | 25887 | tags=67%, list=47%, signal=126% | |
902 | GOLGI VESICLE TRANSPORT | 656 | -0.34 | -1.26 | 0.110 | 0.805 | 0.989 | 25925 | tags=64%, list=47%, signal=120% | |
903 | 3'-UTR-MEDIATED MRNA STABILIZATION | 33 | -0.45 | -1.26 | 0.187 | 0.805 | 0.989 | 22965 | tags=76%, list=42%, signal=131% | |
904 | 7-METHYLGUANOSINE RNA CAPPING | 62 | -0.41 | -1.26 | 0.183 | 0.804 | 0.989 | 17200 | tags=58%, list=31%, signal=85% | |
905 | NEGATIVE REGULATION OF TRANSFERASE ACTIVITY | 637 | -0.33 | -1.26 | 0.088 | 0.803 | 0.989 | 23916 | tags=59%, list=44%, signal=103% | |
906 | CELLULAR RESPONSE TO OXYGEN LEVELS | 250 | -0.32 | -1.26 | 0.097 | 0.803 | 0.989 | 23179 | tags=56%, list=42%, signal=96% | |
907 | PROTEIN K6-LINKED UBIQUITINATION | 19 | -0.44 | -1.26 | 0.219 | 0.802 | 0.989 | 28674 | tags=89%, list=52%, signal=188% | |
908 | SKELETAL MUSCLE TISSUE REGENERATION | 25 | -0.46 | -1.26 | 0.223 | 0.802 | 0.989 | 18711 | tags=64%, list=34%, signal=97% | |
909 | POSITIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 329 | -0.34 | -1.26 | 0.116 | 0.801 | 0.989 | 19464 | tags=52%, list=36%, signal=80% | |
910 | PROTEIN MODIFICATION BY SMALL PROTEIN REMOVAL | 262 | -0.35 | -1.26 | 0.197 | 0.801 | 0.989 | 20641 | tags=56%, list=38%, signal=89% | |
911 | PEROXISOME FISSION | 26 | -0.43 | -1.26 | 0.188 | 0.801 | 0.989 | 17894 | tags=58%, list=33%, signal=86% | |
912 | RESPONSE TO IRON ION | 49 | -0.38 | -1.26 | 0.198 | 0.801 | 0.989 | 7049 | tags=31%, list=13%, signal=35% | |
913 | MRNA TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 19 | -0.41 | -1.26 | 0.182 | 0.803 | 0.989 | 13945 | tags=47%, list=26%, signal=64% | |
914 | KINETOCHORE ASSEMBLY | 8 | -0.50 | -1.26 | 0.216 | 0.804 | 0.989 | 16669 | tags=63%, list=30%, signal=90% | |
915 | REGULATION OF NECROTIC CELL DEATH | 61 | -0.38 | -1.26 | 0.170 | 0.803 | 0.989 | 18588 | tags=57%, list=34%, signal=87% | |
916 | FATTY ACID BETA-OXIDATION USING ACYL-COA DEHYDROGENASE | 11 | -0.53 | -1.26 | 0.211 | 0.803 | 0.989 | 19579 | tags=82%, list=36%, signal=127% | |
917 | TRANSCRIPTION ELONGATION FROM RNA POLYMERASE I PROMOTER | 65 | -0.37 | -1.26 | 0.209 | 0.803 | 0.989 | 19487 | tags=57%, list=36%, signal=88% | |
918 | RESPONSE TO IONIZING RADIATION | 169 | -0.36 | -1.26 | 0.151 | 0.804 | 0.989 | 19314 | tags=56%, list=35%, signal=86% | |
919 | POSITIVE REGULATION OF PROTEOLYSIS | 703 | -0.34 | -1.26 | 0.084 | 0.805 | 0.989 | 20672 | tags=55%, list=38%, signal=88% | |
920 | NEGATIVE REGULATION OF RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 88 | -0.37 | -1.26 | 0.237 | 0.805 | 0.989 | 25775 | tags=69%, list=47%, signal=131% | |
921 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO TELOMERE | 19 | -0.50 | -1.26 | 0.229 | 0.804 | 0.989 | 25365 | tags=89%, list=46%, signal=167% | |
922 | NEGATIVE REGULATION OF TRANSLATIONAL INITIATION IN RESPONSE TO STRESS | 13 | -0.49 | -1.26 | 0.198 | 0.804 | 0.989 | 5681 | tags=46%, list=10%, signal=51% | |
923 | CITRATE METABOLIC PROCESS | 62 | -0.41 | -1.26 | 0.228 | 0.803 | 0.989 | 23065 | tags=71%, list=42%, signal=123% | |
924 | MITOTIC CELL CYCLE CHECKPOINT | 339 | -0.36 | -1.26 | 0.139 | 0.802 | 0.989 | 24611 | tags=65%, list=45%, signal=118% | |
925 | CELLULAR RESPONSE TO HEAT | 219 | -0.34 | -1.26 | 0.134 | 0.802 | 0.989 | 23874 | tags=62%, list=44%, signal=110% | |
926 | 7-METHYLGUANOSINE MRNA CAPPING | 58 | -0.42 | -1.26 | 0.176 | 0.802 | 0.989 | 17200 | tags=60%, list=31%, signal=88% | |
927 | PURINE-CONTAINING COMPOUND SALVAGE | 22 | -0.44 | -1.25 | 0.187 | 0.802 | 0.989 | 26419 | tags=82%, list=48%, signal=158% | |
928 | RNA CAPPING | 65 | -0.40 | -1.25 | 0.178 | 0.802 | 0.989 | 13001 | tags=49%, list=24%, signal=65% | |
929 | REGULATION OF NUCLEAR CELL CYCLE DNA REPLICATION | 17 | -0.45 | -1.25 | 0.222 | 0.802 | 0.989 | 2700 | tags=29%, list=5%, signal=31% | |
930 | NEGATIVE REGULATION OF CIRCADIAN RHYTHM | 19 | -0.43 | -1.25 | 0.153 | 0.801 | 0.989 | 23849 | tags=68%, list=44%, signal=121% | |
931 | STRESS GRANULE ASSEMBLY | 35 | -0.39 | -1.25 | 0.183 | 0.802 | 0.989 | 5338 | tags=29%, list=10%, signal=32% | |
932 | NEGATIVE REGULATION OF SEQUENCE-SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 282 | -0.30 | -1.25 | 0.118 | 0.801 | 0.989 | 22223 | tags=51%, list=41%, signal=85% | |
933 | PURINE NUCLEOSIDE DIPHOSPHATE METABOLIC PROCESS | 101 | -0.34 | -1.25 | 0.197 | 0.800 | 0.989 | 20756 | tags=51%, list=38%, signal=83% | |
934 | PURINE RIBONUCLEOSIDE DIPHOSPHATE METABOLIC PROCESS | 101 | -0.34 | -1.25 | 0.197 | 0.800 | 0.989 | 20756 | tags=51%, list=38%, signal=83% | |
935 | MITOTIC SPINDLE ASSEMBLY CHECKPOINT | 89 | -0.38 | -1.25 | 0.224 | 0.801 | 0.989 | 17763 | tags=53%, list=32%, signal=78% | |
936 | NEGATIVE REGULATION OF UBIQUITIN PROTEIN LIGASE ACTIVITY | 89 | -0.38 | -1.25 | 0.224 | 0.800 | 0.989 | 17763 | tags=53%, list=32%, signal=78% | |
937 | REGULATION OF SYMBIOSIS, ENCOMPASSING MUTUALISM THROUGH PARASITISM | 475 | -0.34 | -1.25 | 0.092 | 0.800 | 0.990 | 18993 | tags=51%, list=35%, signal=77% | |
938 | HYDROGEN SULFIDE METABOLIC PROCESS | 8 | -0.56 | -1.25 | 0.225 | 0.800 | 0.990 | 8123 | tags=50%, list=15%, signal=59% | |
939 | ACETYL-COA BIOSYNTHETIC PROCESS | 20 | -0.43 | -1.25 | 0.201 | 0.800 | 0.990 | 20147 | tags=65%, list=37%, signal=103% | |
940 | REGULATION OF PROTEIN OLIGOMERIZATION | 69 | -0.35 | -1.25 | 0.146 | 0.799 | 0.990 | 18905 | tags=49%, list=35%, signal=75% | |
941 | RESPONSE TO ESTROGEN | 135 | -0.30 | -1.25 | 0.121 | 0.800 | 0.990 | 15684 | tags=37%, list=29%, signal=52% | |
942 | ATRIAL SEPTUM MORPHOGENESIS | 24 | -0.40 | -1.25 | 0.187 | 0.799 | 0.990 | 11290 | tags=42%, list=21%, signal=52% | |
943 | DNA MODIFICATION | 161 | -0.31 | -1.25 | 0.127 | 0.799 | 0.990 | 23736 | tags=55%, list=43%, signal=96% | |
944 | CELLULAR CARBOHYDRATE CATABOLIC PROCESS | 56 | -0.37 | -1.25 | 0.174 | 0.799 | 0.990 | 19181 | tags=55%, list=35%, signal=85% | |
945 | CELLULAR RESPONSE TO GLUCOSE STARVATION | 63 | -0.39 | -1.25 | 0.202 | 0.799 | 0.990 | 26294 | tags=73%, list=48%, signal=141% | |
946 | ENDOSOMAL TRANSPORT | 459 | -0.35 | -1.25 | 0.110 | 0.798 | 0.990 | 20155 | tags=55%, list=37%, signal=86% | |
947 | PROTEIN PEPTIDYL-PROLYL ISOMERIZATION | 30 | -0.43 | -1.25 | 0.251 | 0.798 | 0.990 | 19924 | tags=67%, list=36%, signal=105% | |
948 | RIBONUCLEOSIDE DIPHOSPHATE METABOLIC PROCESS | 106 | -0.34 | -1.25 | 0.184 | 0.798 | 0.990 | 20756 | tags=52%, list=38%, signal=83% | |
949 | REGULATION OF T CELL ACTIVATION VIA T CELL RECEPTOR CONTACT WITH ANTIGEN BOUND TO MHC MOLECULE ON ANTIGEN PRESENTING CELL | 10 | -0.52 | -1.25 | 0.232 | 0.799 | 0.990 | 13890 | tags=50%, list=25%, signal=67% | |
950 | REGULATION OF TRANSCRIPTION OF NUCLEAR LARGE RRNA TRANSCRIPT FROM RNA POLYMERASE I PROMOTER | 23 | -0.41 | -1.25 | 0.219 | 0.798 | 0.990 | 15050 | tags=52%, list=28%, signal=72% | |
951 | ACTIN FILAMENT ORGANIZATION | 283 | -0.32 | -1.25 | 0.135 | 0.797 | 0.990 | 19184 | tags=48%, list=35%, signal=73% | |
952 | POSITIVE REGULATION OF VIRAL TRANSCRIPTION | 130 | -0.37 | -1.25 | 0.169 | 0.797 | 0.990 | 17946 | tags=54%, list=33%, signal=80% | |
953 | REGULATION OF B CELL MEDIATED IMMUNITY | 38 | -0.41 | -1.25 | 0.210 | 0.796 | 0.990 | 5307 | tags=32%, list=10%, signal=35% | |
954 | NEGATIVE REGULATION OF METAPHASE/ANAPHASE TRANSITION OF CELL CYCLE | 97 | -0.38 | -1.25 | 0.233 | 0.795 | 0.990 | 17763 | tags=54%, list=32%, signal=79% | |
955 | POSITIVE REGULATION OF LAMELLIPODIUM ASSEMBLY | 25 | -0.42 | -1.25 | 0.229 | 0.796 | 0.990 | 19435 | tags=56%, list=36%, signal=87% | |
956 | SPINDLE ORGANIZATION | 178 | -0.35 | -1.25 | 0.096 | 0.795 | 0.990 | 21598 | tags=60%, list=40%, signal=98% | |
957 | ANDROGEN RECEPTOR SIGNALING PATHWAY | 54 | -0.37 | -1.25 | 0.163 | 0.795 | 0.990 | 21542 | tags=57%, list=39%, signal=95% | |
958 | REGULATION OF CHOLESTEROL ESTERIFICATION | 17 | -0.50 | -1.25 | 0.251 | 0.794 | 0.990 | 19183 | tags=65%, list=35%, signal=100% | |
959 | REGULATION OF MITOTIC CELL CYCLE PHASE TRANSITION | 533 | -0.34 | -1.25 | 0.125 | 0.796 | 0.990 | 25456 | tags=63%, list=47%, signal=117% | |
960 | REGULATION OF T-CIRCLE FORMATION | 19 | -0.43 | -1.25 | 0.202 | 0.796 | 0.990 | 16208 | tags=53%, list=30%, signal=75% | |
961 | FERRIC IRON TRANSPORT | 77 | -0.36 | -1.25 | 0.175 | 0.796 | 0.990 | 13799 | tags=43%, list=25%, signal=57% | |
962 | TRANSFERRIN TRANSPORT | 77 | -0.36 | -1.25 | 0.175 | 0.795 | 0.990 | 13799 | tags=43%, list=25%, signal=57% | |
963 | TRIVALENT INORGANIC CATION TRANSPORT | 77 | -0.36 | -1.25 | 0.175 | 0.794 | 0.990 | 13799 | tags=43%, list=25%, signal=57% | |
964 | POSITIVE REGULATION OF B CELL MEDIATED IMMUNITY | 20 | -0.45 | -1.25 | 0.228 | 0.793 | 0.990 | 5072 | tags=35%, list=9%, signal=39% | |
965 | POSITIVE REGULATION OF IMMUNOGLOBULIN MEDIATED IMMUNE RESPONSE | 20 | -0.45 | -1.25 | 0.228 | 0.792 | 0.990 | 5072 | tags=35%, list=9%, signal=39% | |
966 | VERY-LOW-DENSITY LIPOPROTEIN PARTICLE ASSEMBLY | 12 | -0.48 | -1.25 | 0.209 | 0.793 | 0.990 | 24670 | tags=75%, list=45%, signal=137% | |
967 | PROTEIN UBIQUITINATION INVOLVED IN UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 117 | -0.36 | -1.25 | 0.119 | 0.794 | 0.990 | 23787 | tags=61%, list=44%, signal=107% | |
968 | GLUTATHIONE BIOSYNTHETIC PROCESS | 24 | -0.43 | -1.25 | 0.200 | 0.794 | 0.990 | 25424 | tags=79%, list=47%, signal=148% | |
969 | ESTABLISHMENT OF VESICLE LOCALIZATION | 355 | -0.34 | -1.25 | 0.143 | 0.795 | 0.990 | 24678 | tags=63%, list=45%, signal=114% | |
970 | ESTABLISHMENT OR MAINTENANCE OF CELL POLARITY | 191 | -0.31 | -1.25 | 0.111 | 0.794 | 0.990 | 21154 | tags=49%, list=39%, signal=79% | |
971 | MONOSACCHARIDE TRANSPORT | 139 | -0.30 | -1.25 | 0.080 | 0.794 | 0.990 | 14921 | tags=37%, list=27%, signal=51% | |
972 | REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 56 | -0.36 | -1.25 | 0.177 | 0.793 | 0.990 | 21048 | tags=57%, list=38%, signal=93% | |
973 | GLUCOSE 6-PHOSPHATE METABOLIC PROCESS | 26 | -0.41 | -1.25 | 0.203 | 0.793 | 0.990 | 27357 | tags=73%, list=50%, signal=146% | |
974 | PURINE NUCLEOTIDE BIOSYNTHETIC PROCESS | 167 | -0.32 | -1.25 | 0.205 | 0.792 | 0.990 | 12116 | tags=37%, list=22%, signal=47% | |
975 | RESPONSE TO TUMOR NECROSIS FACTOR | 391 | -0.32 | -1.25 | 0.098 | 0.791 | 0.990 | 18818 | tags=47%, list=34%, signal=72% | |
976 | RESPONSE TO INDOLE-3-METHANOL | 15 | -0.48 | -1.25 | 0.209 | 0.791 | 0.990 | 24945 | tags=87%, list=46%, signal=159% | |
977 | CELLULAR RESPONSE TO INDOLE-3-METHANOL | 15 | -0.48 | -1.25 | 0.209 | 0.790 | 0.990 | 24945 | tags=87%, list=46%, signal=159% | |
978 | TRANSITION METAL ION HOMEOSTASIS | 217 | -0.33 | -1.25 | 0.103 | 0.793 | 0.990 | 19987 | tags=52%, list=37%, signal=81% | |
979 | CHROMOSOME CONDENSATION | 29 | -0.37 | -1.25 | 0.162 | 0.793 | 0.990 | 13423 | tags=41%, list=25%, signal=55% | |
980 | NEGATIVE REGULATION OF TELOMERE MAINTENANCE | 89 | -0.35 | -1.25 | 0.169 | 0.793 | 0.990 | 21013 | tags=53%, list=38%, signal=86% | |
981 | APOPTOTIC SIGNALING PATHWAY | 704 | -0.32 | -1.24 | 0.092 | 0.797 | 0.991 | 21348 | tags=52%, list=39%, signal=85% | |
982 | REGULATION OF CYCLIN-DEPENDENT PROTEIN KINASE ACTIVITY | 198 | -0.32 | -1.24 | 0.121 | 0.797 | 0.991 | 23980 | tags=58%, list=44%, signal=102% | |
983 | INTERNAL PROTEIN AMINO ACID ACETYLATION | 226 | -0.34 | -1.24 | 0.161 | 0.797 | 0.991 | 20339 | tags=53%, list=37%, signal=83% | |
984 | POSITIVE REGULATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 60 | -0.40 | -1.24 | 0.229 | 0.797 | 0.991 | 18530 | tags=57%, list=34%, signal=86% | |
985 | POSITIVE REGULATION OF CREB TRANSCRIPTION FACTOR ACTIVITY | 29 | -0.37 | -1.24 | 0.176 | 0.798 | 0.991 | 6423 | tags=31%, list=12%, signal=35% | |
986 | CELLULAR RESPONSE TO RADIATION | 273 | -0.32 | -1.24 | 0.101 | 0.800 | 0.991 | 19314 | tags=49%, list=35%, signal=75% | |
987 | REGULATION OF RHODOPSIN MEDIATED SIGNALING PATHWAY | 80 | -0.33 | -1.24 | 0.190 | 0.800 | 0.991 | 20665 | tags=49%, list=38%, signal=78% | |
988 | POSITIVE REGULATION OF AUTOPHAGOSOME ASSEMBLY | 27 | -0.43 | -1.24 | 0.164 | 0.802 | 0.991 | 27620 | tags=89%, list=51%, signal=180% | |
989 | NEGATIVE REGULATION OF GRANULOCYTE DIFFERENTIATION | 23 | -0.41 | -1.24 | 0.217 | 0.801 | 0.992 | 27116 | tags=61%, list=50%, signal=121% | |
990 | REGULATION OF LAMELLIPODIUM ORGANIZATION | 76 | -0.34 | -1.24 | 0.157 | 0.801 | 0.992 | 15662 | tags=41%, list=29%, signal=57% | |
991 | ETHANOLAMINE-CONTAINING COMPOUND METABOLIC PROCESS | 134 | -0.32 | -1.24 | 0.149 | 0.802 | 0.992 | 24425 | tags=58%, list=45%, signal=105% | |
992 | FATTY ACID ELONGATION, UNSATURATED FATTY ACID | 10 | -0.49 | -1.24 | 0.197 | 0.802 | 0.992 | 19619 | tags=70%, list=36%, signal=109% | |
993 | REGULATION OF MAMMARY GLAND EPITHELIAL CELL PROLIFERATION | 17 | -0.44 | -1.24 | 0.198 | 0.802 | 0.992 | 19930 | tags=59%, list=36%, signal=93% | |
994 | REGULATION OF CELLULAR RESPONSE TO HEAT | 185 | -0.34 | -1.24 | 0.180 | 0.802 | 0.992 | 23874 | tags=63%, list=44%, signal=111% | |
995 | REGULATION BY VIRUS OF VIRAL PROTEIN LEVELS IN HOST CELL | 23 | -0.45 | -1.24 | 0.246 | 0.802 | 0.992 | 15463 | tags=57%, list=28%, signal=79% | |
996 | LYMPHOCYTE APOPTOTIC PROCESS | 16 | -0.45 | -1.24 | 0.211 | 0.802 | 0.992 | 17275 | tags=63%, list=32%, signal=91% | |
997 | REGULATION OF RIBONUCLEASE ACTIVITY | 12 | -0.49 | -1.24 | 0.219 | 0.802 | 0.992 | 15284 | tags=67%, list=28%, signal=93% | |
998 | LYSINE METABOLIC PROCESS | 22 | -0.44 | -1.24 | 0.189 | 0.802 | 0.992 | 21683 | tags=73%, list=40%, signal=120% | |
999 | LYSINE CATABOLIC PROCESS | 22 | -0.44 | -1.24 | 0.189 | 0.801 | 0.992 | 21683 | tags=73%, list=40%, signal=120% | |
1000 | REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 56 | -0.37 | -1.24 | 0.221 | 0.800 | 0.992 | 24882 | tags=70%, list=46%, signal=128% | |
1001 | ALDITOL PHOSPHATE METABOLIC PROCESS | 44 | -0.36 | -1.24 | 0.181 | 0.802 | 0.992 | 23706 | tags=61%, list=43%, signal=108% | |
1002 | MRNA PROCESSING | 601 | -0.36 | -1.24 | 0.226 | 0.802 | 0.992 | 21191 | tags=58%, list=39%, signal=94% | |
1003 | RIBONUCLEOSIDE METABOLIC PROCESS | 338 | -0.32 | -1.24 | 0.182 | 0.801 | 0.992 | 20756 | tags=53%, list=38%, signal=85% | |
1004 | STEM CELL POPULATION MAINTENANCE | 157 | -0.32 | -1.24 | 0.146 | 0.801 | 0.992 | 21259 | tags=51%, list=39%, signal=83% | |
1005 | RESPONSE TO HYDROPEROXIDE | 13 | -0.50 | -1.24 | 0.226 | 0.801 | 0.992 | 21371 | tags=77%, list=39%, signal=126% | |
1006 | REGULATION OF NFAT PROTEIN IMPORT INTO NUCLEUS | 32 | -0.39 | -1.24 | 0.221 | 0.801 | 0.992 | 20838 | tags=56%, list=38%, signal=91% | |
1007 | REGULATION OF DNA DAMAGE CHECKPOINT | 18 | -0.44 | -1.24 | 0.177 | 0.800 | 0.992 | 21204 | tags=67%, list=39%, signal=109% | |
1008 | RESPIRATORY CHAIN COMPLEX III ASSEMBLY | 3 | -0.67 | -1.24 | 0.116 | 0.800 | 0.992 | 6296 | tags=67%, list=12%, signal=75% | |
1009 | MITOCHONDRIAL RESPIRATORY CHAIN COMPLEX III ASSEMBLY | 3 | -0.67 | -1.24 | 0.116 | 0.799 | 0.992 | 6296 | tags=67%, list=12%, signal=75% | |
1010 | MITOCHONDRIAL RESPIRATORY CHAIN COMPLEX III BIOGENESIS | 3 | -0.67 | -1.24 | 0.116 | 0.799 | 0.992 | 6296 | tags=67%, list=12%, signal=75% | |
1011 | ORGANOPHOSPHATE BIOSYNTHETIC PROCESS | 732 | -0.32 | -1.24 | 0.066 | 0.798 | 0.992 | 24207 | tags=59%, list=44%, signal=105% | |
1012 | CELLULAR IRON ION HOMEOSTASIS | 134 | -0.33 | -1.24 | 0.179 | 0.800 | 0.992 | 16320 | tags=45%, list=30%, signal=64% | |
1013 | FOLIC ACID-CONTAINING COMPOUND METABOLIC PROCESS | 52 | -0.36 | -1.24 | 0.205 | 0.800 | 0.992 | 20054 | tags=46%, list=37%, signal=73% | |
1014 | NEGATIVE REGULATION OF MITOTIC METAPHASE/ANAPHASE TRANSITION | 96 | -0.38 | -1.24 | 0.256 | 0.799 | 0.992 | 17763 | tags=53%, list=32%, signal=79% | |
1015 | MITOTIC SPINDLE CHECKPOINT | 96 | -0.38 | -1.24 | 0.256 | 0.798 | 0.992 | 17763 | tags=53%, list=32%, signal=79% | |
1016 | NEGATIVE REGULATION OF MITOTIC SISTER CHROMATID SEPARATION | 96 | -0.38 | -1.24 | 0.256 | 0.798 | 0.992 | 17763 | tags=53%, list=32%, signal=79% | |
1017 | REGULATION OF LOW-DENSITY LIPOPROTEIN PARTICLE CLEARANCE | 12 | -0.47 | -1.24 | 0.209 | 0.798 | 0.992 | 7462 | tags=33%, list=14%, signal=39% | |
1018 | NEGATIVE REGULATION OF PROTEIN KINASE B SIGNALING | 58 | -0.35 | -1.24 | 0.153 | 0.798 | 0.992 | 18246 | tags=48%, list=33%, signal=72% | |
1019 | CYTOSKELETAL ANCHORING AT NUCLEAR MEMBRANE | 17 | -0.44 | -1.24 | 0.206 | 0.798 | 0.992 | 24311 | tags=71%, list=44%, signal=127% | |
1020 | PHOSPHATIDYLSERINE ACYL-CHAIN REMODELING | 29 | -0.38 | -1.24 | 0.217 | 0.798 | 0.992 | 23706 | tags=66%, list=43%, signal=116% | |
1021 | POSITIVE REGULATION OF HISTONE MODIFICATION | 150 | -0.32 | -1.24 | 0.185 | 0.798 | 0.992 | 15813 | tags=42%, list=29%, signal=59% | |
1022 | HISTONE H2A ACETYLATION | 30 | -0.44 | -1.24 | 0.270 | 0.798 | 0.992 | 14941 | tags=57%, list=27%, signal=78% | |
1023 | PROTEIN DEPOLYMERIZATION | 35 | -0.39 | -1.24 | 0.237 | 0.798 | 0.992 | 26373 | tags=74%, list=48%, signal=143% | |
1024 | ESTABLISHMENT OF MITOTIC SPINDLE ORIENTATION | 19 | -0.43 | -1.24 | 0.221 | 0.798 | 0.992 | 26797 | tags=79%, list=49%, signal=155% | |
1025 | POSITIVE REGULATION OF PROTEASOMAL PROTEIN CATABOLIC PROCESS | 148 | -0.35 | -1.24 | 0.155 | 0.797 | 0.992 | 25897 | tags=67%, list=47%, signal=127% | |
1026 | TRNA MODIFICATION | 89 | -0.36 | -1.24 | 0.256 | 0.796 | 0.992 | 21883 | tags=61%, list=40%, signal=101% | |
1027 | REGULATION OF PROTEASOMAL UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 305 | -0.36 | -1.23 | 0.154 | 0.796 | 0.992 | 26137 | tags=69%, list=48%, signal=131% | |
1028 | GPI ANCHOR BIOSYNTHETIC PROCESS | 64 | -0.39 | -1.23 | 0.160 | 0.796 | 0.992 | 27888 | tags=81%, list=51%, signal=166% | |
1029 | MAINTENANCE OF ORGAN IDENTITY | 14 | -0.45 | -1.23 | 0.225 | 0.795 | 0.992 | 20582 | tags=64%, list=38%, signal=103% | |
1030 | MANNOSYLATION | 25 | -0.43 | -1.23 | 0.252 | 0.795 | 0.992 | 21988 | tags=72%, list=40%, signal=120% | |
1031 | L-CYSTINE TRANSPORT | 11 | -0.49 | -1.23 | 0.193 | 0.794 | 0.992 | 25451 | tags=91%, list=47%, signal=170% | |
1032 | GENE SILENCING | 320 | -0.34 | -1.23 | 0.119 | 0.795 | 0.992 | 22469 | tags=57%, list=41%, signal=97% | |
1033 | REGULATION OF DNA-TEMPLATED TRANSCRIPTION IN RESPONSE TO STRESS | 159 | -0.33 | -1.23 | 0.203 | 0.795 | 0.992 | 22396 | tags=55%, list=41%, signal=92% | |
1034 | NEURAL TUBE CLOSURE | 57 | -0.37 | -1.23 | 0.206 | 0.795 | 0.992 | 9411 | tags=37%, list=17%, signal=44% | |
1035 | PRIMARY NEURAL TUBE FORMATION | 57 | -0.37 | -1.23 | 0.206 | 0.794 | 0.992 | 9411 | tags=37%, list=17%, signal=44% | |
1036 | TUBE CLOSURE | 57 | -0.37 | -1.23 | 0.206 | 0.794 | 0.992 | 9411 | tags=37%, list=17%, signal=44% | |
1037 | GPI ANCHOR METABOLIC PROCESS | 72 | -0.38 | -1.23 | 0.139 | 0.793 | 0.992 | 29349 | tags=83%, list=54%, signal=180% | |
1038 | RESPONSE TO AMINO ACID | 55 | -0.36 | -1.23 | 0.233 | 0.793 | 0.992 | 20659 | tags=58%, list=38%, signal=93% | |
1039 | TRANSITION METAL ION TRANSPORT | 172 | -0.31 | -1.23 | 0.156 | 0.793 | 0.992 | 14847 | tags=40%, list=27%, signal=55% | |
1040 | PROTEIN K11-LINKED DEUBIQUITINATION | 24 | -0.39 | -1.23 | 0.216 | 0.792 | 0.992 | 10555 | tags=38%, list=19%, signal=46% | |
1041 | POSITIVE REGULATION OF JUN KINASE ACTIVITY | 92 | -0.34 | -1.23 | 0.110 | 0.791 | 0.992 | 17587 | tags=48%, list=32%, signal=70% | |
1042 | LIPOPROTEIN METABOLIC PROCESS | 207 | -0.30 | -1.23 | 0.107 | 0.791 | 0.992 | 22419 | tags=52%, list=41%, signal=87% | |
1043 | PROTEIN SUMOYLATION | 274 | -0.35 | -1.23 | 0.155 | 0.791 | 0.992 | 24486 | tags=63%, list=45%, signal=113% | |
1044 | REGULATION OF INTERLEUKIN-8 PRODUCTION | 121 | -0.34 | -1.23 | 0.206 | 0.790 | 0.992 | 19886 | tags=46%, list=36%, signal=73% | |
1045 | NUCLEOTIDE CATABOLIC PROCESS | 109 | -0.33 | -1.23 | 0.109 | 0.791 | 0.992 | 16617 | tags=43%, list=30%, signal=62% | |
1046 | MAINTENANCE OF PROTEIN LOCATION IN NUCLEUS | 37 | -0.40 | -1.23 | 0.169 | 0.792 | 0.992 | 22427 | tags=68%, list=41%, signal=114% | |
1047 | REGULATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 66 | -0.41 | -1.23 | 0.232 | 0.792 | 0.992 | 18530 | tags=58%, list=34%, signal=87% | |
1048 | LAMELLIPODIUM ASSEMBLY | 58 | -0.37 | -1.23 | 0.185 | 0.791 | 0.992 | 13099 | tags=41%, list=24%, signal=54% | |
1049 | CELLULAR RESPONSE TO LIGHT STIMULUS | 197 | -0.31 | -1.23 | 0.132 | 0.791 | 0.992 | 19231 | tags=47%, list=35%, signal=73% | |
1050 | REGULATION OF PROTEASOMAL PROTEIN CATABOLIC PROCESS | 350 | -0.35 | -1.23 | 0.136 | 0.791 | 0.992 | 26137 | tags=67%, list=48%, signal=128% | |
1051 | SPINDLE ASSEMBLY CHECKPOINT | 93 | -0.37 | -1.23 | 0.252 | 0.793 | 0.992 | 24353 | tags=65%, list=45%, signal=116% | |
1052 | PROTEASOME ASSEMBLY | 13 | -0.49 | -1.23 | 0.227 | 0.792 | 0.992 | 6692 | tags=46%, list=12%, signal=53% | |
1053 | CORTICOSTEROID RECEPTOR SIGNALING PATHWAY | 16 | -0.47 | -1.23 | 0.180 | 0.791 | 0.992 | 20883 | tags=75%, list=38%, signal=121% | |
1054 | GLUCOCORTICOID RECEPTOR SIGNALING PATHWAY | 16 | -0.47 | -1.23 | 0.180 | 0.790 | 0.992 | 20883 | tags=75%, list=38%, signal=121% | |
1055 | CELLULAR RESPONSE TO EXOGENOUS DSRNA | 21 | -0.42 | -1.23 | 0.211 | 0.793 | 0.992 | 15412 | tags=52%, list=28%, signal=73% | |
1056 | NEGATIVE REGULATION OF CATION CHANNEL ACTIVITY | 67 | -0.32 | -1.23 | 0.226 | 0.794 | 0.992 | 26192 | tags=60%, list=48%, signal=114% | |
1057 | SULFUR AMINO ACID CATABOLIC PROCESS | 21 | -0.37 | -1.23 | 0.228 | 0.796 | 0.992 | 19133 | tags=57%, list=35%, signal=88% | |
1058 | COENZYME METABOLIC PROCESS | 406 | -0.31 | -1.23 | 0.147 | 0.796 | 0.992 | 20310 | tags=49%, list=37%, signal=77% | |
1059 | PHOSPHOLIPID SCRAMBLING | 8 | -0.52 | -1.23 | 0.224 | 0.796 | 0.992 | 20281 | tags=63%, list=37%, signal=99% | |
1060 | REGULATION OF DNA-TEMPLATED TRANSCRIPTION, ELONGATION | 70 | -0.36 | -1.23 | 0.189 | 0.796 | 0.992 | 15920 | tags=46%, list=29%, signal=64% | |
1061 | NEGATIVE REGULATION OF NIK/NF-KAPPAB SIGNALING | 7 | -0.52 | -1.23 | 0.244 | 0.796 | 0.992 | 20713 | tags=71%, list=38%, signal=115% | |
1062 | NEGATIVE REGULATION OF LEUKOCYTE APOPTOTIC PROCESS | 49 | -0.38 | -1.23 | 0.191 | 0.795 | 0.992 | 21387 | tags=57%, list=39%, signal=94% | |
1063 | CELLULAR CARBOHYDRATE METABOLIC PROCESS | 197 | -0.31 | -1.23 | 0.128 | 0.795 | 0.992 | 20532 | tags=49%, list=38%, signal=79% | |
1064 | REGULATION OF VIRAL PROCESS | 453 | -0.33 | -1.23 | 0.113 | 0.794 | 0.992 | 18993 | tags=50%, list=35%, signal=76% | |
1065 | NEGATIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 27 | -0.39 | -1.23 | 0.224 | 0.794 | 0.992 | 23748 | tags=63%, list=43%, signal=111% | |
1066 | ANTIGEN PROCESSING AND PRESENTATION OF PEPTIDE ANTIGEN | 405 | -0.33 | -1.23 | 0.206 | 0.793 | 0.992 | 25887 | tags=65%, list=47%, signal=123% | |
1067 | RNA SPLICING, VIA TRANSESTERIFICATION REACTIONS | 505 | -0.36 | -1.23 | 0.242 | 0.794 | 0.992 | 21191 | tags=58%, list=39%, signal=94% | |
1068 | EXECUTION PHASE OF APOPTOSIS | 167 | -0.33 | -1.23 | 0.200 | 0.794 | 0.992 | 18745 | tags=50%, list=34%, signal=76% | |
1069 | PROTEIN K29-LINKED UBIQUITINATION | 16 | -0.44 | -1.23 | 0.241 | 0.793 | 0.992 | 14294 | tags=56%, list=26%, signal=76% | |
1070 | POSITIVE REGULATION OF MITOCHONDRIAL TRANSLATION | 7 | -0.55 | -1.23 | 0.215 | 0.794 | 0.992 | 10265 | tags=57%, list=19%, signal=70% | |
1071 | RNA METHYLATION | 47 | -0.41 | -1.23 | 0.220 | 0.794 | 0.992 | 14669 | tags=53%, list=27%, signal=73% | |
1072 | NEGATIVE REGULATION OF MITOTIC CELL CYCLE | 462 | -0.34 | -1.23 | 0.161 | 0.795 | 0.992 | 24220 | tags=62%, list=44%, signal=111% | |
1073 | PYRIMIDINE-CONTAINING COMPOUND METABOLIC PROCESS | 115 | -0.32 | -1.23 | 0.177 | 0.795 | 0.992 | 21468 | tags=55%, list=39%, signal=90% | |
1074 | JAK-STAT CASCADE | 130 | -0.30 | -1.23 | 0.189 | 0.794 | 0.992 | 26669 | tags=59%, list=49%, signal=115% | |
1075 | STAT CASCADE | 130 | -0.30 | -1.23 | 0.189 | 0.794 | 0.992 | 26669 | tags=59%, list=49%, signal=115% | |
1076 | REGULATION OF PROTEIN POLYUBIQUITINATION | 31 | -0.38 | -1.23 | 0.224 | 0.794 | 0.992 | 29055 | tags=81%, list=53%, signal=172% | |
1077 | CELLULAR MODIFIED AMINO ACID BIOSYNTHETIC PROCESS | 60 | -0.34 | -1.23 | 0.204 | 0.794 | 0.992 | 22656 | tags=55%, list=41%, signal=94% | |
1078 | MORPHOGENESIS OF AN ENDOTHELIUM | 33 | -0.36 | -1.23 | 0.201 | 0.793 | 0.992 | 12728 | tags=36%, list=23%, signal=47% | |
1079 | POST-GOLGI VESICLE-MEDIATED TRANSPORT | 262 | -0.34 | -1.23 | 0.151 | 0.793 | 0.992 | 22018 | tags=57%, list=40%, signal=95% | |
1080 | GLOMERULAR EPITHELIAL CELL DIFFERENTIATION | 32 | -0.36 | -1.23 | 0.200 | 0.792 | 0.992 | 18177 | tags=47%, list=33%, signal=70% | |
1081 | TERMINATION OF RNA POLYMERASE I TRANSCRIPTION | 70 | -0.36 | -1.22 | 0.241 | 0.793 | 0.992 | 19487 | tags=56%, list=36%, signal=86% | |
1082 | REGULATION OF NEPHRON TUBULE EPITHELIAL CELL DIFFERENTIATION | 28 | -0.40 | -1.22 | 0.230 | 0.792 | 0.992 | 17093 | tags=50%, list=31%, signal=73% | |
1083 | CELLULAR RESPONSE TO INTERFERON-BETA | 19 | -0.43 | -1.22 | 0.190 | 0.792 | 0.992 | 11548 | tags=47%, list=21%, signal=60% | |
1084 | MITOCHONDRIAL CALCIUM ION HOMEOSTASIS | 23 | -0.40 | -1.22 | 0.199 | 0.792 | 0.992 | 8238 | tags=39%, list=15%, signal=46% | |
1085 | REGULATION OF UBIQUITIN HOMEOSTASIS | 11 | -0.45 | -1.22 | 0.201 | 0.792 | 0.992 | 28674 | tags=91%, list=52%, signal=191% | |
1086 | PURINE-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 195 | -0.31 | -1.22 | 0.205 | 0.793 | 0.992 | 26419 | tags=61%, list=48%, signal=118% | |
1087 | LEUKOTRIENE METABOLIC PROCESS | 44 | -0.36 | -1.22 | 0.226 | 0.792 | 0.992 | 28804 | tags=77%, list=53%, signal=163% | |
1088 | PEPTIDYL-LYSINE ACETYLATION | 222 | -0.33 | -1.22 | 0.180 | 0.792 | 0.992 | 20339 | tags=52%, list=37%, signal=83% | |
1089 | PROTEIN DEUBIQUITINATION | 231 | -0.34 | -1.22 | 0.230 | 0.792 | 0.992 | 20641 | tags=55%, list=38%, signal=87% | |
1090 | GENE SILENCING BY RNA | 270 | -0.34 | -1.22 | 0.128 | 0.792 | 0.992 | 22469 | tags=57%, list=41%, signal=97% | |
1091 | PHOSPHATIDYLINOSITOL BIOSYNTHETIC PROCESS | 218 | -0.34 | -1.22 | 0.083 | 0.791 | 0.992 | 27515 | tags=70%, list=50%, signal=141% | |
1092 | CARBON CATABOLITE REGULATION OF TRANSCRIPTION | 12 | -0.45 | -1.22 | 0.238 | 0.791 | 0.992 | 19273 | tags=58%, list=35%, signal=90% | |
1093 | NEUTROPHIL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 10 | -0.49 | -1.22 | 0.190 | 0.791 | 0.992 | 20187 | tags=70%, list=37%, signal=111% | |
1094 | REGULATION OF WNT SIGNALING PATHWAY | 594 | -0.30 | -1.22 | 0.152 | 0.793 | 0.992 | 20764 | tags=49%, list=38%, signal=78% | |
1095 | VESICLE LOCALIZATION | 368 | -0.34 | -1.22 | 0.154 | 0.793 | 0.992 | 19176 | tags=52%, list=35%, signal=79% | |
1096 | NEGATIVE REGULATION OF PROTEIN SERINE/THREONINE KINASE ACTIVITY | 226 | -0.32 | -1.22 | 0.134 | 0.793 | 0.992 | 23888 | tags=58%, list=44%, signal=102% | |
1097 | INOSITOL PHOSPHATE METABOLIC PROCESS | 116 | -0.33 | -1.22 | 0.123 | 0.793 | 0.992 | 23100 | tags=58%, list=42%, signal=100% | |
1098 | DNA DAMAGE CHECKPOINT | 315 | -0.35 | -1.22 | 0.145 | 0.793 | 0.992 | 20654 | tags=58%, list=38%, signal=93% | |
1099 | GLYCOSYL COMPOUND METABOLIC PROCESS | 429 | -0.32 | -1.22 | 0.161 | 0.793 | 0.992 | 21434 | tags=55%, list=39%, signal=89% | |
1100 | NEGATIVE REGULATION OF CELL CYCLE PROCESS | 491 | -0.33 | -1.22 | 0.136 | 0.794 | 0.992 | 23423 | tags=59%, list=43%, signal=102% | |
1101 | CELLULAR CARBOHYDRATE BIOSYNTHETIC PROCESS | 68 | -0.34 | -1.22 | 0.228 | 0.793 | 0.992 | 27375 | tags=65%, list=50%, signal=129% | |
1102 | DNA BIOSYNTHETIC PROCESS | 138 | -0.35 | -1.22 | 0.226 | 0.793 | 0.992 | 17205 | tags=51%, list=31%, signal=74% | |
1103 | DETERMINATION OF PANCREATIC LEFT/RIGHT ASYMMETRY | 13 | -0.49 | -1.22 | 0.255 | 0.792 | 0.992 | 12002 | tags=54%, list=22%, signal=69% | |
1104 | CLEAVAGE FURROW FORMATION | 19 | -0.43 | -1.22 | 0.249 | 0.791 | 0.992 | 23744 | tags=74%, list=43%, signal=130% | |
1105 | REGULATION OF GLYCOPROTEIN METABOLIC PROCESS | 66 | -0.35 | -1.22 | 0.167 | 0.791 | 0.992 | 20018 | tags=53%, list=37%, signal=84% | |
1106 | ESTABLISHMENT OF MITOTIC SPINDLE LOCALIZATION | 29 | -0.42 | -1.22 | 0.224 | 0.790 | 0.992 | 16307 | tags=55%, list=30%, signal=79% | |
1107 | REGULATION OF RIG-I SIGNALING PATHWAY | 25 | -0.39 | -1.22 | 0.230 | 0.791 | 0.993 | 5285 | tags=28%, list=10%, signal=31% | |
1108 | REGULATION OF VIRAL TRANSCRIPTION | 187 | -0.36 | -1.22 | 0.122 | 0.791 | 0.993 | 17224 | tags=51%, list=32%, signal=74% | |
1109 | PEPTIDYL-LYSINE DEACETYLATION | 18 | -0.41 | -1.22 | 0.238 | 0.791 | 0.993 | 17225 | tags=50%, list=32%, signal=73% | |
1110 | RNA SPLICING, VIA TRANSESTERIFICATION REACTIONS WITH BULGED ADENOSINE AS NUCLEOPHILE | 497 | -0.36 | -1.22 | 0.252 | 0.791 | 0.993 | 21191 | tags=58%, list=39%, signal=94% | |
1111 | MRNA SPLICING, VIA SPLICEOSOME | 497 | -0.36 | -1.22 | 0.252 | 0.790 | 0.993 | 21191 | tags=58%, list=39%, signal=94% | |
1112 | ORGANOPHOSPHATE ESTER TRANSPORT | 117 | -0.32 | -1.22 | 0.163 | 0.791 | 0.993 | 19183 | tags=46%, list=35%, signal=71% | |
1113 | REGULATION OF ENDOPLASMIC RETICULUM STRESS-INDUCED INTRINSIC APOPTOTIC SIGNALING PATHWAY | 41 | -0.38 | -1.22 | 0.221 | 0.791 | 0.993 | 19715 | tags=59%, list=36%, signal=91% | |
1114 | REGULATION OF CELL PROLIFERATION INVOLVED IN HEART MORPHOGENESIS | 12 | -0.46 | -1.22 | 0.247 | 0.791 | 0.993 | 23703 | tags=75%, list=43%, signal=132% | |
1115 | REGULATION OF PROTEIN ACETYLATION | 126 | -0.31 | -1.22 | 0.162 | 0.791 | 0.993 | 15434 | tags=41%, list=28%, signal=57% | |
1116 | EPHRIN RECEPTOR SIGNALING PATHWAY | 271 | -0.30 | -1.22 | 0.130 | 0.791 | 0.993 | 16503 | tags=41%, list=30%, signal=59% | |
1117 | GUANOSINE-CONTAINING COMPOUND METABOLIC PROCESS | 53 | -0.38 | -1.22 | 0.216 | 0.790 | 0.993 | 20481 | tags=62%, list=37%, signal=99% | |
1118 | CELLULAR RESPONSE TO UV-B | 11 | -0.49 | -1.22 | 0.235 | 0.789 | 0.993 | 6642 | tags=36%, list=12%, signal=41% | |
1119 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE I PROMOTER | 57 | -0.36 | -1.22 | 0.211 | 0.790 | 0.993 | 23033 | tags=63%, list=42%, signal=109% | |
1120 | ACTIVATION OF JUN KINASE ACTIVITY | 54 | -0.34 | -1.22 | 0.165 | 0.789 | 0.993 | 9442 | tags=33%, list=17%, signal=40% | |
1121 | REGULATION OF BINDING | 484 | -0.30 | -1.22 | 0.081 | 0.789 | 0.993 | 19906 | tags=45%, list=36%, signal=71% | |
1122 | REGULATION OF VIRAL LIFE CYCLE | 416 | -0.33 | -1.22 | 0.115 | 0.789 | 0.993 | 18993 | tags=50%, list=35%, signal=77% | |
1123 | CELL-SUBSTRATE ADHERENS JUNCTION ASSEMBLY | 51 | -0.33 | -1.22 | 0.184 | 0.789 | 0.993 | 14948 | tags=39%, list=27%, signal=54% | |
1124 | FOCAL ADHESION ASSEMBLY | 51 | -0.33 | -1.22 | 0.184 | 0.788 | 0.993 | 14948 | tags=39%, list=27%, signal=54% | |
1125 | RNA POLYADENYLATION | 65 | -0.39 | -1.22 | 0.255 | 0.788 | 0.993 | 20918 | tags=66%, list=38%, signal=107% | |
1126 | RESPONSE TO INTERFERON-BETA | 32 | -0.42 | -1.22 | 0.272 | 0.787 | 0.993 | 24118 | tags=72%, list=44%, signal=129% | |
1127 | PURINE RIBONUCLEOTIDE METABOLIC PROCESS | 396 | -0.30 | -1.22 | 0.198 | 0.787 | 0.993 | 21242 | tags=49%, list=39%, signal=80% | |
1128 | GLYCEROPHOSPHOLIPID BIOSYNTHETIC PROCESS | 436 | -0.32 | -1.22 | 0.112 | 0.787 | 0.993 | 24207 | tags=59%, list=44%, signal=106% | |
1129 | GLIAL CELL DIFFERENTIATION | 114 | -0.32 | -1.22 | 0.141 | 0.786 | 0.993 | 26582 | tags=66%, list=49%, signal=128% | |
1130 | LIPID CATABOLIC PROCESS | 256 | -0.30 | -1.22 | 0.170 | 0.786 | 0.993 | 23991 | tags=57%, list=44%, signal=100% | |
1131 | NEGATIVE REGULATION OF MYOTUBE DIFFERENTIATION | 31 | -0.41 | -1.22 | 0.260 | 0.786 | 0.993 | 18530 | tags=55%, list=34%, signal=83% | |
1132 | DNA REPLICATION INITIATION | 27 | -0.41 | -1.22 | 0.258 | 0.786 | 0.993 | 22812 | tags=67%, list=42%, signal=114% | |
1133 | ADIPOSE TISSUE DEVELOPMENT | 19 | -0.41 | -1.22 | 0.232 | 0.785 | 0.993 | 2377 | tags=26%, list=4%, signal=28% | |
1134 | MARGINAL ZONE B CELL DIFFERENTIATION | 14 | -0.40 | -1.22 | 0.198 | 0.784 | 0.993 | 11535 | tags=36%, list=21%, signal=45% | |
1135 | POSITIVE REGULATION OF DNA REPAIR | 70 | -0.34 | -1.22 | 0.274 | 0.785 | 0.993 | 22559 | tags=57%, list=41%, signal=97% | |
1136 | NEGATIVE REGULATION OF MRNA PROCESSING | 64 | -0.37 | -1.22 | 0.225 | 0.784 | 0.993 | 23769 | tags=61%, list=43%, signal=108% | |
1137 | SPINDLE CHECKPOINT | 104 | -0.36 | -1.22 | 0.254 | 0.784 | 0.993 | 24353 | tags=64%, list=45%, signal=116% | |
1138 | IMPORT ACROSS PLASMA MEMBRANE | 12 | -0.44 | -1.22 | 0.262 | 0.784 | 0.993 | 22671 | tags=75%, list=41%, signal=128% | |
1139 | C-TERMINAL PROTEIN LIPIDATION | 56 | -0.39 | -1.22 | 0.182 | 0.784 | 0.993 | 22240 | tags=68%, list=41%, signal=114% | |
1140 | POSITIVE REGULATION OF INTERLEUKIN-4 PRODUCTION | 29 | -0.42 | -1.22 | 0.268 | 0.784 | 0.993 | 14287 | tags=41%, list=26%, signal=56% | |
1141 | ANTIGEN PROCESSING AND PRESENTATION | 445 | -0.33 | -1.22 | 0.219 | 0.785 | 0.993 | 21511 | tags=56%, list=39%, signal=92% | |
1142 | POSITIVE REGULATION OF VIRAL PROCESS | 262 | -0.35 | -1.22 | 0.176 | 0.784 | 0.994 | 21191 | tags=57%, list=39%, signal=92% | |
1143 | POSTTRANSCRIPTIONAL REGULATION OF GENE EXPRESSION | 822 | -0.33 | -1.22 | 0.174 | 0.784 | 0.994 | 22704 | tags=58%, list=42%, signal=97% | |
1144 | REGULATION OF FIBROBLAST MIGRATION | 49 | -0.35 | -1.22 | 0.232 | 0.783 | 0.994 | 10100 | tags=31%, list=18%, signal=38% | |
1145 | REGULATION OF NAD(P)H OXIDASE ACTIVITY | 7 | -0.51 | -1.21 | 0.251 | 0.784 | 0.994 | 19714 | tags=71%, list=36%, signal=112% | |
1146 | NEURON REMODELING | 12 | -0.42 | -1.21 | 0.222 | 0.785 | 0.994 | 16503 | tags=58%, list=30%, signal=84% | |
1147 | REGULATION OF CELL CYCLE PHASE TRANSITION | 583 | -0.32 | -1.21 | 0.141 | 0.785 | 0.994 | 25186 | tags=61%, list=46%, signal=112% | |
1148 | RIBOSE PHOSPHATE METABOLIC PROCESS | 434 | -0.30 | -1.21 | 0.210 | 0.785 | 0.994 | 21242 | tags=50%, list=39%, signal=80% | |
1149 | POSITIVE REGULATION OF CHOLESTEROL EFFLUX | 22 | -0.40 | -1.21 | 0.241 | 0.785 | 0.994 | 19886 | tags=55%, list=36%, signal=86% | |
1150 | BONE REMODELING | 35 | -0.35 | -1.21 | 0.204 | 0.785 | 0.994 | 20589 | tags=43%, list=38%, signal=69% | |
1151 | NEGATIVE REGULATION OF PROTEIN OLIGOMERIZATION | 25 | -0.37 | -1.21 | 0.227 | 0.784 | 0.994 | 15791 | tags=40%, list=29%, signal=56% | |
1152 | PRODUCTION OF MIRNAS INVOLVED IN GENE SILENCING BY MIRNA | 56 | -0.37 | -1.21 | 0.259 | 0.785 | 0.994 | 18797 | tags=54%, list=34%, signal=82% | |
1153 | LIPID MODIFICATION | 221 | -0.34 | -1.21 | 0.177 | 0.785 | 0.994 | 25136 | tags=63%, list=46%, signal=116% | |
1154 | ACTIN FILAMENT BUNDLE ASSEMBLY | 101 | -0.32 | -1.21 | 0.156 | 0.784 | 0.994 | 19623 | tags=48%, list=36%, signal=74% | |
1155 | ACTIN FILAMENT BUNDLE ORGANIZATION | 101 | -0.32 | -1.21 | 0.156 | 0.784 | 0.994 | 19623 | tags=48%, list=36%, signal=74% | |
1156 | PTERIDINE-CONTAINING COMPOUND METABOLIC PROCESS | 57 | -0.35 | -1.21 | 0.254 | 0.783 | 0.994 | 20054 | tags=46%, list=37%, signal=72% | |
1157 | PROTEIN LIPIDATION | 138 | -0.34 | -1.21 | 0.140 | 0.783 | 0.994 | 27520 | tags=72%, list=50%, signal=144% | |
1158 | LIPOPROTEIN BIOSYNTHETIC PROCESS | 138 | -0.34 | -1.21 | 0.140 | 0.782 | 0.994 | 27520 | tags=72%, list=50%, signal=144% | |
1159 | SNRNA METABOLIC PROCESS | 56 | -0.38 | -1.21 | 0.148 | 0.781 | 0.994 | 22091 | tags=64%, list=40%, signal=108% | |
1160 | REGULATION OF GLYCOPROTEIN BIOSYNTHETIC PROCESS | 57 | -0.35 | -1.21 | 0.169 | 0.781 | 0.994 | 20018 | tags=53%, list=37%, signal=83% | |
1161 | PHOSPHOLIPID BIOSYNTHETIC PROCESS | 459 | -0.32 | -1.21 | 0.121 | 0.780 | 0.994 | 24207 | tags=59%, list=44%, signal=106% | |
1162 | POSITIVE REGULATION OF MULTI-ORGANISM PROCESS | 340 | -0.33 | -1.21 | 0.140 | 0.781 | 0.994 | 21191 | tags=54%, list=39%, signal=87% | |
1163 | RIBONUCLEOTIDE METABOLIC PROCESS | 407 | -0.30 | -1.21 | 0.203 | 0.780 | 0.994 | 21242 | tags=49%, list=39%, signal=80% | |
1164 | PENTOSE-PHOSPHATE SHUNT | 25 | -0.41 | -1.21 | 0.228 | 0.780 | 0.994 | 27357 | tags=76%, list=50%, signal=152% | |
1165 | CELL REDOX HOMEOSTASIS | 94 | -0.33 | -1.21 | 0.212 | 0.779 | 0.994 | 12991 | tags=39%, list=24%, signal=52% | |
1166 | AUTOPHAGY | 653 | -0.31 | -1.21 | 0.173 | 0.780 | 0.994 | 14229 | tags=40%, list=26%, signal=53% | |
1167 | PURINE NUCLEOTIDE METABOLIC PROCESS | 444 | -0.30 | -1.21 | 0.192 | 0.780 | 0.994 | 27023 | tags=61%, list=49%, signal=119% | |
1168 | REGULATION OF MULTICELLULAR ORGANISM GROWTH | 68 | -0.32 | -1.21 | 0.225 | 0.779 | 0.994 | 22720 | tags=46%, list=42%, signal=78% | |
1169 | RETROGRADE TRANSPORT, ENDOSOME TO GOLGI | 148 | -0.34 | -1.21 | 0.215 | 0.779 | 0.994 | 27788 | tags=69%, list=51%, signal=140% | |
1170 | PORE COMPLEX ASSEMBLY | 21 | -0.44 | -1.21 | 0.255 | 0.779 | 0.994 | 23874 | tags=76%, list=44%, signal=135% | |
1171 | LEUKOCYTE APOPTOTIC PROCESS | 18 | -0.43 | -1.21 | 0.221 | 0.778 | 0.994 | 17275 | tags=61%, list=32%, signal=89% | |
1172 | INORGANIC CATION IMPORT INTO CELL | 30 | -0.38 | -1.21 | 0.215 | 0.778 | 0.994 | 7049 | tags=30%, list=13%, signal=34% | |
1173 | INORGANIC ION IMPORT INTO CELL | 30 | -0.38 | -1.21 | 0.215 | 0.777 | 0.994 | 7049 | tags=30%, list=13%, signal=34% | |
1174 | MITOTIC SISTER CHROMATID SEGREGATION | 139 | -0.35 | -1.21 | 0.176 | 0.777 | 0.994 | 16669 | tags=50%, list=30%, signal=71% | |
1175 | IRON ION IMPORT | 41 | -0.36 | -1.21 | 0.214 | 0.776 | 0.994 | 14547 | tags=39%, list=27%, signal=53% | |
1176 | NEGATIVE REGULATION OF PROTEIN ACETYLATION | 35 | -0.39 | -1.21 | 0.198 | 0.776 | 0.994 | 15434 | tags=49%, list=28%, signal=68% | |
1177 | EPITHELIAL CILIUM MOVEMENT INVOLVED IN DETERMINATION OF LEFT/RIGHT ASYMMETRY | 13 | -0.51 | -1.21 | 0.284 | 0.778 | 0.994 | 17345 | tags=69%, list=32%, signal=101% | |
1178 | REGULATION OF PROTEIN POLYMERIZATION | 228 | -0.31 | -1.21 | 0.165 | 0.777 | 0.994 | 19703 | tags=47%, list=36%, signal=74% | |
1179 | POSITIVE REGULATION OF CHROMATIN MODIFICATION | 162 | -0.32 | -1.21 | 0.208 | 0.778 | 0.994 | 15813 | tags=41%, list=29%, signal=57% | |
1180 | SYNAPTIC VESICLE EXOCYTOSIS | 33 | -0.36 | -1.21 | 0.258 | 0.778 | 0.994 | 9883 | tags=33%, list=18%, signal=41% | |
1181 | MAINTENANCE OF CELL NUMBER | 162 | -0.31 | -1.21 | 0.181 | 0.777 | 0.994 | 21259 | tags=50%, list=39%, signal=82% | |
1182 | PHOSPHATIDIC ACID BIOSYNTHETIC PROCESS | 67 | -0.33 | -1.21 | 0.223 | 0.777 | 0.994 | 23397 | tags=60%, list=43%, signal=104% | |
1183 | PHOSPHATIDIC ACID METABOLIC PROCESS | 67 | -0.33 | -1.21 | 0.223 | 0.777 | 0.994 | 23397 | tags=60%, list=43%, signal=104% | |
1184 | REGULATION OF PEPTIDYL-LYSINE ACETYLATION | 113 | -0.31 | -1.21 | 0.167 | 0.776 | 0.994 | 15434 | tags=42%, list=28%, signal=58% | |
1185 | CARDIOLIPIN ACYL-CHAIN REMODELING | 12 | -0.44 | -1.21 | 0.266 | 0.776 | 0.994 | 16851 | tags=58%, list=31%, signal=84% | |
1186 | CELL CYCLE PHASE TRANSITION | 631 | -0.33 | -1.21 | 0.163 | 0.776 | 0.994 | 20613 | tags=53%, list=38%, signal=85% | |
1187 | NEGATIVE REGULATION OF MRNA METABOLIC PROCESS | 73 | -0.36 | -1.21 | 0.221 | 0.775 | 0.994 | 24251 | tags=62%, list=44%, signal=111% | |
1188 | REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 151 | -0.32 | -1.21 | 0.211 | 0.775 | 0.994 | 22858 | tags=54%, list=42%, signal=93% | |
1189 | UDP-GLUCOSE METABOLIC PROCESS | 13 | -0.46 | -1.21 | 0.267 | 0.777 | 0.994 | 15247 | tags=54%, list=28%, signal=75% | |
1190 | NEGATIVE REGULATION OF FIBROBLAST PROLIFERATION | 47 | -0.35 | -1.21 | 0.173 | 0.776 | 0.994 | 25937 | tags=64%, list=47%, signal=121% | |
1191 | TRICARBOXYLIC ACID CYCLE | 51 | -0.40 | -1.21 | 0.286 | 0.776 | 0.994 | 23065 | tags=69%, list=42%, signal=119% | |
1192 | REGULATION OF UBIQUITIN PROTEIN LIGASE ACTIVITY | 112 | -0.37 | -1.21 | 0.238 | 0.776 | 0.994 | 23731 | tags=64%, list=43%, signal=113% | |
1193 | NEGATIVE REGULATION OF NUCLEAR DIVISION | 130 | -0.35 | -1.21 | 0.240 | 0.776 | 0.994 | 17763 | tags=50%, list=32%, signal=74% | |
1194 | INTERNAL PEPTIDYL-LYSINE ACETYLATION | 220 | -0.33 | -1.21 | 0.198 | 0.775 | 0.994 | 20339 | tags=52%, list=37%, signal=82% | |
1195 | COENZYME BIOSYNTHETIC PROCESS | 165 | -0.34 | -1.21 | 0.139 | 0.775 | 0.994 | 24625 | tags=63%, list=45%, signal=114% | |
1196 | ENDOTHELIAL CELL FATE COMMITMENT | 19 | -0.40 | -1.21 | 0.237 | 0.775 | 0.994 | 24501 | tags=68%, list=45%, signal=124% | |
1197 | POSITIVE REGULATION OF VIRAL LIFE CYCLE | 243 | -0.35 | -1.21 | 0.183 | 0.774 | 0.994 | 21191 | tags=57%, list=39%, signal=93% | |
1198 | POSITIVE REGULATION OF PROTEASOMAL UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 134 | -0.36 | -1.21 | 0.210 | 0.774 | 0.994 | 25897 | tags=69%, list=47%, signal=132% | |
1199 | MITOTIC NUCLEAR ENVELOPE DISASSEMBLY | 111 | -0.35 | -1.21 | 0.165 | 0.773 | 0.994 | 23874 | tags=59%, list=44%, signal=105% | |
1200 | MEMBRANE DISASSEMBLY | 111 | -0.35 | -1.21 | 0.165 | 0.773 | 0.994 | 23874 | tags=59%, list=44%, signal=105% | |
1201 | NUCLEAR ENVELOPE DISASSEMBLY | 111 | -0.35 | -1.21 | 0.165 | 0.772 | 0.994 | 23874 | tags=59%, list=44%, signal=105% | |
1202 | MICROTUBULE CYTOSKELETON ORGANIZATION INVOLVED IN MITOSIS | 59 | -0.37 | -1.21 | 0.235 | 0.772 | 0.994 | 23423 | tags=68%, list=43%, signal=118% | |
1203 | POSITIVE REGULATION OF INTERLEUKIN-8 PRODUCTION | 77 | -0.37 | -1.21 | 0.225 | 0.772 | 0.994 | 15663 | tags=43%, list=29%, signal=60% | |
1204 | MITOTIC CELL CYCLE PHASE TRANSITION | 619 | -0.33 | -1.21 | 0.169 | 0.773 | 0.994 | 20613 | tags=53%, list=38%, signal=85% | |
1205 | PURINE-CONTAINING COMPOUND METABOLIC PROCESS | 519 | -0.30 | -1.21 | 0.196 | 0.772 | 0.994 | 27023 | tags=61%, list=49%, signal=119% | |
1206 | GLYCEROLIPID BIOSYNTHETIC PROCESS | 529 | -0.32 | -1.21 | 0.084 | 0.773 | 0.994 | 24425 | tags=59%, list=45%, signal=106% | |
1207 | VACUOLE ORGANIZATION | 161 | -0.34 | -1.21 | 0.201 | 0.773 | 0.994 | 27620 | tags=71%, list=51%, signal=143% | |
1208 | NEGATIVE REGULATION OF MRNA POLYADENYLATION | 12 | -0.46 | -1.21 | 0.245 | 0.772 | 0.994 | 19323 | tags=58%, list=35%, signal=90% | |
1209 | REGULATION OF PROTEIN HETERODIMERIZATION ACTIVITY | 18 | -0.42 | -1.21 | 0.221 | 0.772 | 0.994 | 7436 | tags=28%, list=14%, signal=32% | |
1210 | NOTCH SIGNALING PATHWAY | 254 | -0.31 | -1.21 | 0.166 | 0.772 | 0.994 | 25185 | tags=60%, list=46%, signal=110% | |
1211 | POSITIVE REGULATION OF DEACETYLASE ACTIVITY | 23 | -0.42 | -1.21 | 0.272 | 0.772 | 0.995 | 7557 | tags=39%, list=14%, signal=45% | |
1212 | REGULATION OF GENE EXPRESSION, EPIGENETIC | 430 | -0.32 | -1.21 | 0.135 | 0.771 | 0.995 | 22469 | tags=56%, list=41%, signal=94% | |
1213 | POSITIVE REGULATION OF I-KAPPAB KINASE/NF-KAPPAB SIGNALING | 363 | -0.33 | -1.21 | 0.213 | 0.772 | 0.995 | 25677 | tags=65%, list=47%, signal=122% | |
1214 | REGULATION OF SYNAPTIC VESICLE TRANSPORT | 33 | -0.38 | -1.21 | 0.192 | 0.772 | 0.995 | 15593 | tags=45%, list=29%, signal=64% | |
1215 | PHOSPHORYLATED CARBOHYDRATE DEPHOSPHORYLATION | 16 | -0.46 | -1.21 | 0.239 | 0.772 | 0.995 | 18246 | tags=69%, list=33%, signal=103% | |
1216 | INOSITOL PHOSPHATE DEPHOSPHORYLATION | 16 | -0.46 | -1.21 | 0.239 | 0.772 | 0.995 | 18246 | tags=69%, list=33%, signal=103% | |
1217 | NEURON APOPTOTIC PROCESS | 38 | -0.37 | -1.20 | 0.243 | 0.771 | 0.995 | 22028 | tags=61%, list=40%, signal=101% | |
1218 | CELLULAR METABOLIC COMPOUND SALVAGE | 56 | -0.36 | -1.20 | 0.226 | 0.771 | 0.995 | 28039 | tags=75%, list=51%, signal=154% | |
1219 | GENE SILENCING BY MIRNA | 99 | -0.35 | -1.20 | 0.253 | 0.771 | 0.995 | 21868 | tags=59%, list=40%, signal=97% | |
1220 | RENAL FILTRATION CELL DIFFERENTIATION | 31 | -0.36 | -1.20 | 0.246 | 0.771 | 0.995 | 13287 | tags=39%, list=24%, signal=51% | |
1221 | GLOMERULAR VISCERAL EPITHELIAL CELL DIFFERENTIATION | 31 | -0.36 | -1.20 | 0.246 | 0.770 | 0.995 | 13287 | tags=39%, list=24%, signal=51% | |
1222 | ER OVERLOAD RESPONSE | 16 | -0.45 | -1.20 | 0.264 | 0.771 | 0.995 | 22419 | tags=75%, list=41%, signal=127% | |
1223 | REGULATION OF EXOSOMAL SECRETION | 23 | -0.42 | -1.20 | 0.300 | 0.770 | 0.995 | 23401 | tags=74%, list=43%, signal=129% | |
1224 | POSITIVE REGULATION OF EXOSOMAL SECRETION | 23 | -0.42 | -1.20 | 0.300 | 0.770 | 0.995 | 23401 | tags=74%, list=43%, signal=129% | |
1225 | NEGATIVE REGULATION OF CHROMOSOME ORGANIZATION | 273 | -0.33 | -1.20 | 0.181 | 0.769 | 0.995 | 22427 | tags=56%, list=41%, signal=95% | |
1226 | HISTONE H3 DEACETYLATION | 34 | -0.37 | -1.20 | 0.225 | 0.769 | 0.995 | 27572 | tags=71%, list=50%, signal=142% | |
1227 | REGULATION OF APOPTOTIC SIGNALING PATHWAY | 627 | -0.31 | -1.20 | 0.213 | 0.770 | 0.995 | 19715 | tags=49%, list=36%, signal=75% | |
1228 | PROTEIN ACETYLATION | 254 | -0.32 | -1.20 | 0.187 | 0.770 | 0.995 | 20339 | tags=51%, list=37%, signal=80% | |
1229 | CRISTAE FORMATION | 14 | -0.42 | -1.20 | 0.260 | 0.770 | 0.995 | 22659 | tags=64%, list=41%, signal=110% | |
1230 | TETRAHYDROFOLATE METABOLIC PROCESS | 31 | -0.39 | -1.20 | 0.239 | 0.770 | 0.996 | 23005 | tags=61%, list=42%, signal=106% | |
1231 | MEMBRANE REPOLARIZATION | 26 | -0.35 | -1.20 | 0.226 | 0.770 | 0.996 | 16903 | tags=42%, list=31%, signal=61% | |
1232 | NUCLEOTIDE-EXCISION REPAIR, DNA DAMAGE RECOGNITION | 44 | -0.40 | -1.20 | 0.284 | 0.770 | 0.996 | 26583 | tags=77%, list=49%, signal=150% | |
1233 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 195 | -0.30 | -1.20 | 0.171 | 0.772 | 0.996 | 21400 | tags=49%, list=39%, signal=81% | |
1234 | NEGATIVE REGULATION OF CELL CYCLE | 905 | -0.32 | -1.20 | 0.145 | 0.771 | 0.996 | 23334 | tags=57%, list=43%, signal=97% | |
1235 | REGULATED EXOCYTOSIS | 90 | -0.34 | -1.20 | 0.228 | 0.771 | 0.996 | 22018 | tags=54%, list=40%, signal=91% | |
1236 | NEGATIVE REGULATION OF GTPASE ACTIVITY | 66 | -0.33 | -1.20 | 0.216 | 0.770 | 0.996 | 18988 | tags=45%, list=35%, signal=70% | |
1237 | POSITIVE REGULATION OF EXOCYTOSIS | 112 | -0.32 | -1.20 | 0.221 | 0.770 | 0.996 | 24179 | tags=58%, list=44%, signal=104% | |
1238 | NEGATIVE REGULATION OF SMOOTHENED SIGNALING PATHWAY | 37 | -0.34 | -1.20 | 0.242 | 0.770 | 0.996 | 19158 | tags=43%, list=35%, signal=67% | |
1239 | RHODOPSIN MEDIATED SIGNALING PATHWAY | 84 | -0.32 | -1.20 | 0.227 | 0.770 | 0.996 | 19181 | tags=45%, list=35%, signal=70% | |
1240 | HISTONE H2A UBIQUITINATION | 42 | -0.40 | -1.20 | 0.265 | 0.770 | 0.996 | 23276 | tags=71%, list=43%, signal=124% | |
1241 | THIOESTER BIOSYNTHETIC PROCESS | 99 | -0.33 | -1.20 | 0.192 | 0.771 | 0.996 | 24351 | tags=61%, list=45%, signal=109% | |
1242 | ACYL-COA BIOSYNTHETIC PROCESS | 99 | -0.33 | -1.20 | 0.192 | 0.770 | 0.996 | 24351 | tags=61%, list=45%, signal=109% | |
1243 | RESPONSE TO HEAT | 258 | -0.32 | -1.20 | 0.151 | 0.771 | 0.996 | 23874 | tags=59%, list=44%, signal=105% | |
1244 | VERY LONG-CHAIN FATTY ACID METABOLIC PROCESS | 37 | -0.37 | -1.20 | 0.203 | 0.771 | 0.996 | 20089 | tags=57%, list=37%, signal=90% | |
1245 | ORGANIC ACID CATABOLIC PROCESS | 355 | -0.30 | -1.20 | 0.198 | 0.771 | 0.996 | 22512 | tags=52%, list=41%, signal=88% | |
1246 | CARBOXYLIC ACID CATABOLIC PROCESS | 355 | -0.30 | -1.20 | 0.198 | 0.771 | 0.996 | 22512 | tags=52%, list=41%, signal=88% | |
1247 | DNA REPAIR | 809 | -0.33 | -1.20 | 0.145 | 0.770 | 0.996 | 22710 | tags=58%, list=42%, signal=98% | |
1248 | POSITIVE REGULATION OF JNK CASCADE | 174 | -0.31 | -1.20 | 0.197 | 0.771 | 0.996 | 17769 | tags=44%, list=32%, signal=65% | |
1249 | REGULATION OF TROPHOBLAST CELL MIGRATION | 19 | -0.41 | -1.20 | 0.227 | 0.770 | 0.996 | 17726 | tags=53%, list=32%, signal=78% | |
1250 | MECHANORECEPTOR DIFFERENTIATION | 11 | -0.47 | -1.20 | 0.257 | 0.771 | 0.996 | 18665 | tags=64%, list=34%, signal=97% | |
1251 | INNER EAR RECEPTOR CELL DIFFERENTIATION | 11 | -0.47 | -1.20 | 0.257 | 0.770 | 0.996 | 18665 | tags=64%, list=34%, signal=97% | |
1252 | HISTONE H4 ACETYLATION | 107 | -0.34 | -1.20 | 0.262 | 0.770 | 0.996 | 21206 | tags=56%, list=39%, signal=91% | |
1253 | REGULATION OF RECEPTOR CATABOLIC PROCESS | 18 | -0.42 | -1.20 | 0.274 | 0.771 | 0.996 | 13128 | tags=50%, list=24%, signal=66% | |
1254 | DNA DEALKYLATION | 31 | -0.39 | -1.20 | 0.241 | 0.771 | 0.996 | 16813 | tags=52%, list=31%, signal=74% | |
1255 | DOPAMINE RECEPTOR SIGNALING PATHWAY | 35 | -0.35 | -1.20 | 0.265 | 0.773 | 0.996 | 13338 | tags=40%, list=24%, signal=53% | |
1256 | PEPTIDYL-LYSINE MODIFICATION | 673 | -0.32 | -1.20 | 0.221 | 0.774 | 0.996 | 25318 | tags=61%, list=46%, signal=112% | |
1257 | ALPHA-LINOLENIC ACID METABOLIC PROCESS | 30 | -0.39 | -1.20 | 0.242 | 0.773 | 0.996 | 17595 | tags=53%, list=32%, signal=79% | |
1258 | NEGATIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 51 | -0.37 | -1.20 | 0.253 | 0.773 | 0.996 | 24882 | tags=69%, list=46%, signal=126% | |
1259 | NEGATIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO STRESS | 19 | -0.42 | -1.20 | 0.274 | 0.773 | 0.996 | 24082 | tags=79%, list=44%, signal=141% | |
1260 | REGULATION OF GENE SILENCING BY MIRNA | 23 | -0.37 | -1.20 | 0.257 | 0.773 | 0.996 | 16568 | tags=48%, list=30%, signal=69% | |
1261 | REGULATION OF HISTONE UBIQUITINATION | 20 | -0.44 | -1.20 | 0.283 | 0.773 | 0.996 | 29142 | tags=85%, list=53%, signal=182% | |
1262 | POSITIVE REGULATION OF MICROTUBULE POLYMERIZATION OR DEPOLYMERIZATION | 34 | -0.34 | -1.20 | 0.191 | 0.773 | 0.996 | 12208 | tags=35%, list=22%, signal=45% | |
1263 | CELL CYCLE CHECKPOINT | 476 | -0.34 | -1.20 | 0.160 | 0.772 | 0.996 | 24353 | tags=63%, list=45%, signal=112% | |
1264 | BIOTIN METABOLIC PROCESS | 25 | -0.41 | -1.20 | 0.287 | 0.772 | 0.996 | 24095 | tags=72%, list=44%, signal=129% | |
1265 | ATRIAL SEPTUM DEVELOPMENT | 35 | -0.36 | -1.20 | 0.210 | 0.772 | 0.996 | 12002 | tags=37%, list=22%, signal=48% | |
1266 | DNA INTEGRITY CHECKPOINT | 329 | -0.34 | -1.20 | 0.166 | 0.772 | 0.996 | 20654 | tags=57%, list=38%, signal=90% | |
1267 | NEGATIVE REGULATION OF PROTEIN EXIT FROM ENDOPLASMIC RETICULUM | 27 | -0.40 | -1.20 | 0.260 | 0.772 | 0.996 | 24653 | tags=70%, list=45%, signal=128% | |
1268 | NEGATIVE REGULATION OF RETROGRADE PROTEIN TRANSPORT, ER TO CYTOSOL | 27 | -0.40 | -1.20 | 0.260 | 0.771 | 0.996 | 24653 | tags=70%, list=45%, signal=128% | |
1269 | MACROPINOCYTOSIS | 14 | -0.46 | -1.20 | 0.290 | 0.772 | 0.996 | 11904 | tags=50%, list=22%, signal=64% | |
1270 | COPPER ION TRANSPORT | 14 | -0.49 | -1.20 | 0.284 | 0.772 | 0.996 | 14547 | tags=64%, list=27%, signal=88% | |
1271 | REGULATION OF REMOVAL OF SUPEROXIDE RADICALS | 16 | -0.45 | -1.20 | 0.256 | 0.772 | 0.996 | 19469 | tags=63%, list=36%, signal=97% | |
1272 | DETOXIFICATION | 108 | -0.34 | -1.19 | 0.279 | 0.772 | 0.997 | 21008 | tags=54%, list=38%, signal=87% | |
1273 | NEGATIVE REGULATION OF PROTEIN EXPORT FROM NUCLEUS | 19 | -0.42 | -1.19 | 0.249 | 0.772 | 0.997 | 22892 | tags=74%, list=42%, signal=127% | |
1274 | CHOLESTEROL EFFLUX | 46 | -0.36 | -1.19 | 0.269 | 0.771 | 0.997 | 21536 | tags=52%, list=39%, signal=86% | |
1275 | MRNA TRANSCRIPTION | 33 | -0.37 | -1.19 | 0.252 | 0.776 | 0.997 | 13945 | tags=42%, list=26%, signal=57% | |
1276 | SMALL RNA LOADING ONTO RISC | 20 | -0.40 | -1.19 | 0.247 | 0.776 | 0.997 | 13082 | tags=45%, list=24%, signal=59% | |
1277 | GLYCOGEN BIOSYNTHETIC PROCESS | 31 | -0.40 | -1.19 | 0.295 | 0.776 | 0.997 | 19941 | tags=58%, list=36%, signal=91% | |
1278 | GLUCAN BIOSYNTHETIC PROCESS | 31 | -0.40 | -1.19 | 0.295 | 0.775 | 0.997 | 19941 | tags=58%, list=36%, signal=91% | |
1279 | GDP-MANNOSE METABOLIC PROCESS | 12 | -0.50 | -1.19 | 0.301 | 0.775 | 0.997 | 18997 | tags=75%, list=35%, signal=115% | |
1280 | RESPONSE TO TYPE I INTERFERON | 150 | -0.35 | -1.19 | 0.297 | 0.774 | 0.997 | 22839 | tags=59%, list=42%, signal=100% | |
1281 | POSITIVE REGULATION OF EXTRACELLULAR MATRIX DISASSEMBLY | 20 | -0.38 | -1.19 | 0.236 | 0.776 | 0.997 | 18901 | tags=50%, list=35%, signal=76% | |
1282 | POSITIVE REGULATION OF INNATE IMMUNE RESPONSE | 666 | -0.32 | -1.19 | 0.220 | 0.775 | 0.997 | 21479 | tags=53%, list=39%, signal=86% | |
1283 | MRNA 3'-END PROCESSING | 150 | -0.37 | -1.19 | 0.316 | 0.775 | 0.997 | 18099 | tags=55%, list=33%, signal=81% | |
1284 | REGULATION OF TRANSCRIPTION BY GLUCOSE | 11 | -0.47 | -1.19 | 0.274 | 0.776 | 0.997 | 20859 | tags=64%, list=38%, signal=103% | |
1285 | NEURAL TUBE FORMATION | 66 | -0.34 | -1.19 | 0.245 | 0.775 | 0.997 | 11290 | tags=38%, list=21%, signal=48% | |
1286 | MEMBRANE TUBULATION | 20 | -0.39 | -1.19 | 0.266 | 0.776 | 0.997 | 17498 | tags=50%, list=32%, signal=74% | |
1287 | HIPPO SIGNALING | 75 | -0.33 | -1.19 | 0.226 | 0.775 | 0.997 | 18228 | tags=47%, list=33%, signal=70% | |
1288 | REGULATION OF CELLULAR KETONE METABOLIC PROCESS | 335 | -0.30 | -1.19 | 0.226 | 0.775 | 0.997 | 21182 | tags=50%, list=39%, signal=80% | |
1289 | GLYCEROPHOSPHOLIPID METABOLIC PROCESS | 511 | -0.31 | -1.19 | 0.148 | 0.776 | 0.997 | 24207 | tags=58%, list=44%, signal=103% | |
1290 | MAINTENANCE OF PROTEIN LOCATION IN CELL | 142 | -0.30 | -1.19 | 0.185 | 0.775 | 0.997 | 22928 | tags=54%, list=42%, signal=92% | |
1291 | RRNA-CONTAINING RIBONUCLEOPROTEIN COMPLEX EXPORT FROM NUCLEUS | 10 | -0.50 | -1.19 | 0.264 | 0.775 | 0.997 | 24673 | tags=90%, list=45%, signal=164% | |
1292 | REGULATION OF HYDROGEN PEROXIDE-MEDIATED PROGRAMMED CELL DEATH | 17 | -0.40 | -1.19 | 0.241 | 0.776 | 0.997 | 6843 | tags=29%, list=13%, signal=34% | |
1293 | POSITIVE REGULATION OF HEMATOPOIETIC PROGENITOR CELL DIFFERENTIATION | 18 | -0.38 | -1.19 | 0.230 | 0.777 | 0.997 | 2276 | tags=22%, list=4%, signal=23% | |
1294 | ERK1 AND ERK2 CASCADE | 31 | -0.34 | -1.19 | 0.227 | 0.777 | 0.997 | 18711 | tags=48%, list=34%, signal=74% | |
1295 | RNA 3'-END PROCESSING | 172 | -0.36 | -1.19 | 0.301 | 0.777 | 0.997 | 23418 | tags=65%, list=43%, signal=113% | |
1296 | RESPONSE TO HYPOXIA | 371 | -0.28 | -1.19 | 0.195 | 0.778 | 0.997 | 23179 | tags=51%, list=42%, signal=88% | |
1297 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 177 | -0.34 | -1.19 | 0.263 | 0.778 | 0.997 | 21348 | tags=54%, list=39%, signal=88% | |
1298 | POST-TRANSLATIONAL PROTEIN MODIFICATION | 1113 | -0.31 | -1.19 | 0.155 | 0.779 | 0.997 | 24611 | tags=58%, list=45%, signal=103% | |
1299 | NEGATIVE REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 32 | -0.39 | -1.19 | 0.266 | 0.779 | 0.997 | 22721 | tags=63%, list=42%, signal=107% | |
1300 | MITOPHAGY | 337 | -0.29 | -1.19 | 0.241 | 0.778 | 0.997 | 14229 | tags=37%, list=26%, signal=50% | |
1301 | MITOCHONDRION DISASSEMBLY | 337 | -0.29 | -1.19 | 0.241 | 0.778 | 0.997 | 14229 | tags=37%, list=26%, signal=50% | |
1302 | REGULATION OF CYCLIN-DEPENDENT PROTEIN SERINE/THREONINE KINASE ACTIVITY | 160 | -0.30 | -1.19 | 0.170 | 0.777 | 0.997 | 23980 | tags=55%, list=44%, signal=98% | |
1303 | POSITIVE REGULATION OF AUTOPHAGY | 172 | -0.33 | -1.19 | 0.217 | 0.777 | 0.997 | 25040 | tags=65%, list=46%, signal=120% | |
1304 | REGULATION OF TELOMERE MAINTENANCE | 178 | -0.33 | -1.19 | 0.192 | 0.777 | 0.997 | 23455 | tags=57%, list=43%, signal=100% | |
1305 | REGULATION OF PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR SIGNALING PATHWAY | 29 | -0.35 | -1.19 | 0.228 | 0.778 | 0.997 | 15065 | tags=45%, list=28%, signal=62% | |
1306 | TRANSCRIPTION FROM RNA POLYMERASE I PROMOTER | 76 | -0.35 | -1.19 | 0.269 | 0.777 | 0.997 | 19487 | tags=55%, list=36%, signal=86% | |
1307 | AUTOPHAGOSOME ASSEMBLY | 47 | -0.40 | -1.19 | 0.269 | 0.777 | 0.997 | 16178 | tags=57%, list=30%, signal=82% | |
1308 | EMBRYONIC EPITHELIAL TUBE FORMATION | 84 | -0.32 | -1.19 | 0.229 | 0.777 | 0.997 | 17093 | tags=44%, list=31%, signal=64% | |
1309 | NEGATIVE REGULATION OF SEQUESTERING OF TRIGLYCERIDE | 19 | -0.41 | -1.19 | 0.276 | 0.776 | 0.997 | 32127 | tags=95%, list=59%, signal=230% | |
1310 | REGULATION OF ENDOSOME SIZE | 11 | -0.48 | -1.19 | 0.280 | 0.775 | 0.997 | 16344 | tags=64%, list=30%, signal=91% | |
1311 | REGULATION OF NEUTROPHIL CHEMOTAXIS | 37 | -0.37 | -1.19 | 0.252 | 0.776 | 0.997 | 19058 | tags=49%, list=35%, signal=75% | |
1312 | NEGATIVE REGULATION OF SISTER CHROMATID SEGREGATION | 104 | -0.36 | -1.19 | 0.305 | 0.776 | 0.997 | 17763 | tags=51%, list=32%, signal=75% | |
1313 | NEGATIVE REGULATION OF MITOTIC SISTER CHROMATID SEGREGATION | 104 | -0.36 | -1.19 | 0.305 | 0.775 | 0.997 | 17763 | tags=51%, list=32%, signal=75% | |
1314 | NEGATIVE REGULATION OF CHROMOSOME SEGREGATION | 104 | -0.36 | -1.19 | 0.305 | 0.775 | 0.997 | 17763 | tags=51%, list=32%, signal=75% | |
1315 | REGULATION OF STEM CELL POPULATION MAINTENANCE | 37 | -0.36 | -1.19 | 0.236 | 0.774 | 0.997 | 22704 | tags=57%, list=42%, signal=97% | |
1316 | PROTEIN GLYCOSYLATION | 830 | -0.30 | -1.19 | 0.198 | 0.779 | 0.997 | 21164 | tags=50%, list=39%, signal=80% | |
1317 | MACROMOLECULE GLYCOSYLATION | 830 | -0.30 | -1.19 | 0.198 | 0.778 | 0.997 | 21164 | tags=50%, list=39%, signal=80% | |
1318 | REGULATION OF HISTONE ACETYLATION | 105 | -0.31 | -1.19 | 0.173 | 0.777 | 0.997 | 15434 | tags=41%, list=28%, signal=57% | |
1319 | GLYOXYLATE METABOLIC PROCESS | 43 | -0.38 | -1.18 | 0.303 | 0.779 | 0.997 | 23868 | tags=67%, list=44%, signal=120% | |
1320 | MODULATION BY VIRUS OF HOST PROCESS | 130 | -0.35 | -1.18 | 0.280 | 0.778 | 0.998 | 23874 | tags=62%, list=44%, signal=110% | |
1321 | NEGATIVE REGULATION OF PROTEIN KINASE ACTIVITY | 370 | -0.31 | -1.18 | 0.187 | 0.778 | 0.998 | 23916 | tags=56%, list=44%, signal=99% | |
1322 | NEGATIVE REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 76 | -0.32 | -1.18 | 0.231 | 0.778 | 0.998 | 19886 | tags=47%, list=36%, signal=74% | |
1323 | NEGATIVE REGULATION OF INTERFERON-BETA PRODUCTION | 13 | -0.45 | -1.18 | 0.261 | 0.778 | 0.998 | 21210 | tags=62%, list=39%, signal=101% | |
1324 | ACTIVATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 51 | -0.41 | -1.18 | 0.285 | 0.778 | 0.998 | 18530 | tags=59%, list=34%, signal=89% | |
1325 | FREE UBIQUITIN CHAIN POLYMERIZATION | 9 | -0.45 | -1.18 | 0.254 | 0.778 | 0.998 | 28674 | tags=89%, list=52%, signal=187% | |
1326 | CELLULAR COPPER ION HOMEOSTASIS | 13 | -0.46 | -1.18 | 0.270 | 0.778 | 0.998 | 18982 | tags=69%, list=35%, signal=106% | |
1327 | REGULATION OF METAPHASE/ANAPHASE TRANSITION OF CELL CYCLE | 136 | -0.35 | -1.18 | 0.290 | 0.778 | 0.998 | 24486 | tags=64%, list=45%, signal=116% | |
1328 | MAINTENANCE OF LOCATION IN CELL | 164 | -0.30 | -1.18 | 0.167 | 0.778 | 0.998 | 22928 | tags=54%, list=42%, signal=92% | |
1329 | ORGANELLE LOCALIZATION | 652 | -0.32 | -1.18 | 0.189 | 0.778 | 0.998 | 24834 | tags=60%, list=45%, signal=109% | |
1330 | CELLULAR DETOXIFICATION | 107 | -0.33 | -1.18 | 0.295 | 0.778 | 0.998 | 21008 | tags=53%, list=38%, signal=86% | |
1331 | RESPONSE TO OXYGEN LEVELS | 388 | -0.28 | -1.18 | 0.194 | 0.778 | 0.998 | 23179 | tags=52%, list=42%, signal=89% | |
1332 | POLYOL CATABOLIC PROCESS | 23 | -0.42 | -1.18 | 0.275 | 0.777 | 0.998 | 28174 | tags=87%, list=52%, signal=179% | |
1333 | REGULATION OF MITOTIC SISTER CHROMATID SEPARATION | 138 | -0.35 | -1.18 | 0.298 | 0.777 | 0.998 | 24486 | tags=64%, list=45%, signal=115% | |
1334 | SOMATIC STEM CELL DIVISION | 39 | -0.35 | -1.18 | 0.228 | 0.777 | 0.998 | 15881 | tags=44%, list=29%, signal=61% | |
1335 | NEGATIVE REGULATION OF PROTEIN LOCALIZATION TO CELL SURFACE | 20 | -0.38 | -1.18 | 0.270 | 0.777 | 0.998 | 25909 | tags=75%, list=47%, signal=142% | |
1336 | TRANSCRIPTION FROM RNA POLYMERASE III PROMOTER | 98 | -0.34 | -1.18 | 0.239 | 0.776 | 0.998 | 30021 | tags=80%, list=55%, signal=176% | |
1337 | MATERNAL PROCESS INVOLVED IN FEMALE PREGNANCY | 24 | -0.38 | -1.18 | 0.252 | 0.776 | 0.998 | 15325 | tags=42%, list=28%, signal=58% | |
1338 | ACTIVATION OF INNATE IMMUNE RESPONSE | 593 | -0.32 | -1.18 | 0.232 | 0.776 | 0.998 | 21479 | tags=53%, list=39%, signal=87% | |
1339 | ENDODERMAL CELL FATE COMMITMENT | 17 | -0.42 | -1.18 | 0.304 | 0.776 | 0.998 | 21259 | tags=71%, list=39%, signal=115% | |
1340 | SPHINGOSINE-1-PHOSPHATE SIGNALING PATHWAY | 11 | -0.44 | -1.18 | 0.245 | 0.776 | 0.998 | 8191 | tags=27%, list=15%, signal=32% | |
1341 | SPHINGOLIPID MEDIATED SIGNALING PATHWAY | 11 | -0.44 | -1.18 | 0.245 | 0.775 | 0.998 | 8191 | tags=27%, list=15%, signal=32% | |
1342 | GLYCOSYLATION | 838 | -0.30 | -1.18 | 0.205 | 0.775 | 0.998 | 21164 | tags=50%, list=39%, signal=80% | |
1343 | POSITIVE REGULATION OF INTERFERON-GAMMA BIOSYNTHETIC PROCESS | 16 | -0.43 | -1.18 | 0.293 | 0.777 | 0.998 | 25520 | tags=69%, list=47%, signal=129% | |
1344 | GLUTAMATE METABOLIC PROCESS | 46 | -0.38 | -1.18 | 0.231 | 0.779 | 0.998 | 25424 | tags=72%, list=47%, signal=134% | |
1345 | MITOTIC G2 DNA DAMAGE CHECKPOINT | 32 | -0.38 | -1.18 | 0.256 | 0.778 | 0.998 | 14139 | tags=41%, list=26%, signal=55% | |
1346 | RESPONSE TO DECREASED OXYGEN LEVELS | 377 | -0.28 | -1.18 | 0.203 | 0.778 | 0.998 | 23179 | tags=51%, list=42%, signal=88% | |
1347 | NEGATIVE REGULATION OF RAS PROTEIN SIGNAL TRANSDUCTION | 45 | -0.34 | -1.18 | 0.214 | 0.778 | 0.998 | 11102 | tags=36%, list=20%, signal=45% | |
1348 | POSITIVE REGULATION OF ORGANELLE ORGANIZATION | 1099 | -0.29 | -1.18 | 0.172 | 0.777 | 0.998 | 19495 | tags=46%, list=36%, signal=69% | |
1349 | NEGATIVE REGULATION OF MUSCLE CELL DIFFERENTIATION | 81 | -0.31 | -1.18 | 0.238 | 0.778 | 0.998 | 16694 | tags=40%, list=31%, signal=57% | |
1350 | REGULATION OF PROTEIN LOCALIZATION TO CAJAL BODY | 15 | -0.51 | -1.18 | 0.276 | 0.779 | 0.998 | 25365 | tags=93%, list=46%, signal=174% | |
1351 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO CAJAL BODY | 15 | -0.51 | -1.18 | 0.276 | 0.778 | 0.998 | 25365 | tags=93%, list=46%, signal=174% | |
1352 | REGULATION OF ACTIN FILAMENT POLYMERIZATION | 166 | -0.31 | -1.18 | 0.210 | 0.778 | 0.998 | 19703 | tags=48%, list=36%, signal=74% | |
1353 | POSITIVE REGULATION OF MEGAKARYOCYTE DIFFERENTIATION | 13 | -0.41 | -1.18 | 0.285 | 0.777 | 0.998 | 1997 | tags=23%, list=4%, signal=24% | |
1354 | NEGATIVE REGULATION OF B CELL APOPTOTIC PROCESS | 18 | -0.43 | -1.18 | 0.281 | 0.779 | 0.998 | 21048 | tags=67%, list=38%, signal=108% | |
1355 | NUCLEOTIDE TRANSPORT | 33 | -0.38 | -1.18 | 0.287 | 0.779 | 0.998 | 9403 | tags=36%, list=17%, signal=44% | |
1356 | NEGATIVE REGULATION OF MITOTIC NUCLEAR DIVISION | 122 | -0.34 | -1.18 | 0.288 | 0.780 | 0.998 | 17763 | tags=49%, list=32%, signal=73% | |
1357 | POSITIVE REGULATION OF BETA-AMYLOID FORMATION | 14 | -0.48 | -1.18 | 0.307 | 0.780 | 0.998 | 14157 | tags=57%, list=26%, signal=77% | |
1358 | POSITIVE REGULATION OF AMYLOID PRECURSOR PROTEIN CATABOLIC PROCESS | 14 | -0.48 | -1.18 | 0.307 | 0.779 | 0.998 | 14157 | tags=57%, list=26%, signal=77% | |
1359 | NEGATIVE REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 11 | -0.46 | -1.18 | 0.250 | 0.780 | 0.998 | 8091 | tags=45%, list=15%, signal=53% | |
1360 | CARNITINE METABOLIC PROCESS | 21 | -0.39 | -1.18 | 0.284 | 0.780 | 0.998 | 29840 | tags=81%, list=55%, signal=178% | |
1361 | PHOSPHATIDYLCHOLINE BIOSYNTHETIC PROCESS | 49 | -0.34 | -1.18 | 0.260 | 0.780 | 0.998 | 22551 | tags=53%, list=41%, signal=90% | |
1362 | NEGATIVE REGULATION OF CHROMATIN MODIFICATION | 89 | -0.34 | -1.18 | 0.231 | 0.781 | 0.998 | 15434 | tags=45%, list=28%, signal=63% | |
1363 | REGULATION OF INTERLEUKIN-13 SECRETION | 10 | -0.46 | -1.18 | 0.285 | 0.781 | 0.998 | 17156 | tags=50%, list=31%, signal=73% | |
1364 | DSRNA FRAGMENTATION | 58 | -0.35 | -1.18 | 0.283 | 0.781 | 0.998 | 18797 | tags=52%, list=34%, signal=79% | |
1365 | PRODUCTION OF SMALL RNA INVOLVED IN GENE SILENCING BY RNA | 58 | -0.35 | -1.18 | 0.283 | 0.780 | 0.998 | 18797 | tags=52%, list=34%, signal=79% | |
1366 | GLYCEROLIPID METABOLIC PROCESS | 659 | -0.30 | -1.18 | 0.146 | 0.781 | 0.998 | 24425 | tags=57%, list=45%, signal=101% | |
1367 | NEGATIVE REGULATION OF GLYCOGEN METABOLIC PROCESS | 22 | -0.38 | -1.18 | 0.276 | 0.781 | 0.998 | 19317 | tags=55%, list=35%, signal=84% | |
1368 | POSITIVE REGULATION OF SMOOTH MUSCLE CONTRACTION | 13 | -0.46 | -1.18 | 0.302 | 0.780 | 0.998 | 14060 | tags=46%, list=26%, signal=62% | |
1369 | INTRACELLULAR TRANSPORT OF VIRAL PROTEIN IN HOST CELL | 11 | -0.47 | -1.18 | 0.287 | 0.780 | 0.998 | 14736 | tags=55%, list=27%, signal=75% | |
1370 | SYMBIONT INTRACELLULAR PROTEIN TRANSPORT IN HOST | 11 | -0.47 | -1.18 | 0.287 | 0.779 | 0.998 | 14736 | tags=55%, list=27%, signal=75% | |
1371 | INTRACELLULAR PROTEIN TRANSPORT IN OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 11 | -0.47 | -1.18 | 0.287 | 0.779 | 0.998 | 14736 | tags=55%, list=27%, signal=75% | |
1372 | NEGATIVE REGULATION OF TRANSLATION IN RESPONSE TO STRESS | 27 | -0.38 | -1.18 | 0.255 | 0.779 | 0.998 | 8872 | tags=37%, list=16%, signal=44% | |
1373 | PEPTIDYL-ARGININE METHYLATION | 23 | -0.40 | -1.18 | 0.272 | 0.779 | 0.998 | 26114 | tags=78%, list=48%, signal=150% | |
1374 | REGULATION OF MITOTIC METAPHASE/ANAPHASE TRANSITION | 135 | -0.35 | -1.18 | 0.309 | 0.780 | 0.998 | 24486 | tags=64%, list=45%, signal=115% | |
1375 | REGULATION OF MONOCYTE DIFFERENTIATION | 21 | -0.39 | -1.18 | 0.294 | 0.780 | 0.998 | 19607 | tags=57%, list=36%, signal=89% | |
1376 | RNA STABILIZATION | 90 | -0.33 | -1.17 | 0.266 | 0.780 | 0.998 | 22965 | tags=57%, list=42%, signal=98% | |
1377 | FATTY ACID METABOLIC PROCESS | 347 | -0.30 | -1.17 | 0.191 | 0.779 | 0.998 | 28882 | tags=67%, list=53%, signal=142% | |
1378 | CELLULAR RESPONSE TO AMINO ACID STIMULUS | 49 | -0.36 | -1.17 | 0.283 | 0.779 | 0.998 | 11461 | tags=43%, list=21%, signal=54% | |
1379 | PHOSPHOLIPID METABOLIC PROCESS | 567 | -0.30 | -1.17 | 0.149 | 0.778 | 0.998 | 24207 | tags=57%, list=44%, signal=102% | |
1380 | POSITIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 90 | -0.34 | -1.17 | 0.247 | 0.778 | 0.998 | 20347 | tags=54%, list=37%, signal=87% | |
1381 | POSITIVE REGULATION OF TYPE I INTERFERON-MEDIATED SIGNALING PATHWAY | 12 | -0.47 | -1.17 | 0.295 | 0.778 | 0.998 | 19696 | tags=75%, list=36%, signal=117% | |
1382 | REGULATION OF MITOCHONDRIAL FUSION | 11 | -0.45 | -1.17 | 0.259 | 0.778 | 0.998 | 28674 | tags=91%, list=52%, signal=191% | |
1383 | NEGATIVE REGULATION OF TYPE I INTERFERON PRODUCTION | 101 | -0.35 | -1.17 | 0.236 | 0.778 | 0.998 | 27936 | tags=71%, list=51%, signal=145% | |
1384 | CLATHRIN-MEDIATED ENDOCYTOSIS | 57 | -0.34 | -1.17 | 0.248 | 0.778 | 0.998 | 10425 | tags=35%, list=19%, signal=43% | |
1385 | CELLULAR POLYSACCHARIDE METABOLIC PROCESS | 103 | -0.32 | -1.17 | 0.249 | 0.777 | 0.998 | 20229 | tags=50%, list=37%, signal=78% | |
1386 | PURINE NUCLEOTIDE TRANSPORT | 12 | -0.44 | -1.17 | 0.292 | 0.777 | 0.998 | 9403 | tags=33%, list=17%, signal=40% | |
1387 | REGULATION OF JNK CASCADE | 275 | -0.29 | -1.17 | 0.217 | 0.777 | 0.998 | 17769 | tags=43%, list=32%, signal=63% | |
1388 | POSITIVE REGULATION OF NEUTROPHIL MIGRATION | 31 | -0.39 | -1.17 | 0.287 | 0.777 | 0.998 | 19058 | tags=52%, list=35%, signal=79% | |
1389 | REGULATION OF INTRACELLULAR STEROID HORMONE RECEPTOR SIGNALING PATHWAY | 147 | -0.32 | -1.17 | 0.207 | 0.777 | 0.998 | 28737 | tags=67%, list=53%, signal=142% | |
1390 | GOLGI TO PLASMA MEMBRANE PROTEIN TRANSPORT | 62 | -0.35 | -1.17 | 0.272 | 0.777 | 0.998 | 28128 | tags=73%, list=51%, signal=149% | |
1391 | RECEPTOR CATABOLIC PROCESS | 28 | -0.39 | -1.17 | 0.302 | 0.777 | 0.998 | 18203 | tags=54%, list=33%, signal=80% | |
1392 | CELLULAR TRANSITION METAL ION HOMEOSTASIS | 176 | -0.32 | -1.17 | 0.234 | 0.778 | 0.998 | 15573 | tags=43%, list=28%, signal=59% | |
1393 | POSITIVE REGULATION OF T CELL MEDIATED CYTOTOXICITY | 34 | -0.38 | -1.17 | 0.278 | 0.778 | 0.998 | 17332 | tags=50%, list=32%, signal=73% | |
1394 | PHOSPHOLIPID TRANSPORT | 81 | -0.32 | -1.17 | 0.226 | 0.778 | 0.998 | 19183 | tags=46%, list=35%, signal=70% | |
1395 | REGULATION OF INNATE IMMUNE RESPONSE | 876 | -0.30 | -1.17 | 0.251 | 0.777 | 0.998 | 21665 | tags=51%, list=40%, signal=84% | |
1396 | ADHERENS JUNCTION ASSEMBLY | 66 | -0.32 | -1.17 | 0.264 | 0.778 | 0.998 | 15684 | tags=39%, list=29%, signal=55% | |
1397 | RESPONSE TO PROSTAGLANDIN E | 30 | -0.38 | -1.17 | 0.276 | 0.777 | 0.998 | 13452 | tags=40%, list=25%, signal=53% | |
1398 | POSITIVE REGULATION OF CELL MIGRATION BY VASCULAR ENDOTHELIAL GROWTH FACTOR SIGNALING PATHWAY | 14 | -0.44 | -1.17 | 0.271 | 0.777 | 0.998 | 9002 | tags=43%, list=16%, signal=51% | |
1399 | TELOMERE MAINTENANCE VIA TELOMERASE | 33 | -0.37 | -1.17 | 0.277 | 0.777 | 0.998 | 11631 | tags=39%, list=21%, signal=50% | |
1400 | POSTTRANSCRIPTIONAL GENE SILENCING | 113 | -0.34 | -1.17 | 0.275 | 0.777 | 0.998 | 22464 | tags=58%, list=41%, signal=99% | |
1401 | POSITIVE REGULATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC PROCESS | 258 | -0.32 | -1.17 | 0.257 | 0.777 | 0.998 | 18530 | tags=49%, list=34%, signal=74% | |
1402 | MITOTIC SPINDLE ASSEMBLY | 55 | -0.37 | -1.17 | 0.289 | 0.777 | 0.998 | 21547 | tags=64%, list=39%, signal=105% | |
1403 | REGULATION OF MRNA 3'-END PROCESSING | 62 | -0.37 | -1.17 | 0.320 | 0.777 | 0.998 | 20112 | tags=58%, list=37%, signal=92% | |
1404 | L-KYNURENINE METABOLIC PROCESS | 5 | -0.56 | -1.17 | 0.259 | 0.776 | 0.998 | 22310 | tags=80%, list=41%, signal=135% | |
1405 | TRANSCRIPTION INITIATION FROM RNA POLYMERASE II PROMOTER | 647 | -0.30 | -1.17 | 0.193 | 0.776 | 0.998 | 18947 | tags=47%, list=35%, signal=71% | |
1406 | NEGATIVE REGULATION OF GLYCOGEN BIOSYNTHETIC PROCESS | 21 | -0.39 | -1.17 | 0.286 | 0.775 | 0.998 | 19317 | tags=57%, list=35%, signal=88% | |
1407 | ACTIVATION OF PROTEIN KINASE A ACTIVITY | 38 | -0.33 | -1.17 | 0.237 | 0.775 | 0.998 | 20922 | tags=47%, list=38%, signal=77% | |
1408 | NEGATIVE REGULATION OF PEPTIDYL-LYSINE ACETYLATION | 32 | -0.38 | -1.17 | 0.255 | 0.775 | 0.998 | 15434 | tags=50%, list=28%, signal=70% | |
1409 | AEROBIC RESPIRATION | 77 | -0.38 | -1.17 | 0.327 | 0.774 | 0.998 | 22263 | tags=65%, list=41%, signal=109% | |
1410 | POSITIVE REGULATION OF GENE EXPRESSION, EPIGENETIC | 133 | -0.32 | -1.17 | 0.298 | 0.774 | 0.998 | 19487 | tags=50%, list=36%, signal=77% | |
1411 | GRANULOCYTE DIFFERENTIATION | 15 | -0.43 | -1.17 | 0.280 | 0.774 | 0.998 | 22943 | tags=47%, list=42%, signal=80% | |
1412 | REGULATION OF MULTI-ORGANISM PROCESS | 922 | -0.30 | -1.17 | 0.180 | 0.774 | 0.998 | 21607 | tags=51%, list=40%, signal=82% | |
1413 | NEGATIVE REGULATION OF RESPONSE TO DNA DAMAGE STIMULUS | 114 | -0.31 | -1.17 | 0.243 | 0.774 | 0.998 | 21540 | tags=53%, list=39%, signal=87% | |
1414 | REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 246 | -0.32 | -1.17 | 0.262 | 0.774 | 0.998 | 20636 | tags=53%, list=38%, signal=85% | |
1415 | POSTTRANSCRIPTIONAL GENE SILENCING BY RNA | 110 | -0.34 | -1.17 | 0.280 | 0.774 | 0.998 | 22464 | tags=58%, list=41%, signal=99% | |
1416 | REGULATION OF SISTER CHROMATID SEGREGATION | 165 | -0.34 | -1.17 | 0.325 | 0.773 | 0.998 | 24486 | tags=62%, list=45%, signal=113% | |
1417 | REGULATION OF DEFENSE RESPONSE TO VIRUS BY VIRUS | 80 | -0.34 | -1.17 | 0.299 | 0.775 | 0.998 | 14999 | tags=45%, list=27%, signal=62% | |
1418 | CARBOHYDRATE HOMEOSTASIS | 180 | -0.29 | -1.17 | 0.177 | 0.776 | 0.998 | 24557 | tags=56%, list=45%, signal=102% | |
1419 | GLUCOSE HOMEOSTASIS | 180 | -0.29 | -1.17 | 0.177 | 0.775 | 0.998 | 24557 | tags=56%, list=45%, signal=102% | |
1420 | REGULATION OF GRANULOCYTE DIFFERENTIATION | 40 | -0.34 | -1.17 | 0.231 | 0.776 | 0.998 | 27116 | tags=55%, list=50%, signal=109% | |
1421 | RESPONSE TO EPIDERMAL GROWTH FACTOR | 61 | -0.34 | -1.17 | 0.271 | 0.776 | 0.998 | 15828 | tags=44%, list=29%, signal=62% | |
1422 | HISTONE MODIFICATION | 669 | -0.31 | -1.17 | 0.210 | 0.776 | 0.998 | 23488 | tags=56%, list=43%, signal=97% | |
1423 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO CHROMOSOME | 22 | -0.40 | -1.17 | 0.275 | 0.776 | 0.998 | 24022 | tags=73%, list=44%, signal=130% | |
1424 | REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 61 | -0.31 | -1.17 | 0.245 | 0.776 | 0.998 | 21879 | tags=49%, list=40%, signal=82% | |
1425 | NEGATIVE REGULATION OF KINASE ACTIVITY | 397 | -0.30 | -1.17 | 0.188 | 0.777 | 0.998 | 25937 | tags=59%, list=47%, signal=112% | |
1426 | PROTEIN REFOLDING | 42 | -0.38 | -1.17 | 0.295 | 0.777 | 0.998 | 26736 | tags=79%, list=49%, signal=154% | |
1427 | POSITIVE REGULATION OF TELOMERE CAPPING | 41 | -0.35 | -1.17 | 0.304 | 0.779 | 0.998 | 16235 | tags=44%, list=30%, signal=62% | |
1428 | NUCLEOTIDE-EXCISION REPAIR, DNA GAP FILLING | 40 | -0.38 | -1.17 | 0.312 | 0.779 | 0.998 | 19793 | tags=60%, list=36%, signal=94% | |
1429 | PROTEIN LOCALIZATION TO ENDOSOME | 25 | -0.38 | -1.17 | 0.307 | 0.780 | 0.998 | 21406 | tags=60%, list=39%, signal=99% | |
1430 | POSITIVE REGULATION OF RESPONSE TO EXTRACELLULAR STIMULUS | 113 | -0.34 | -1.17 | 0.268 | 0.780 | 0.998 | 24159 | tags=65%, list=44%, signal=116% | |
1431 | POSITIVE REGULATION OF RESPONSE TO NUTRIENT LEVELS | 113 | -0.34 | -1.17 | 0.268 | 0.779 | 0.998 | 24159 | tags=65%, list=44%, signal=116% | |
1432 | HISTONE ACETYLATION | 211 | -0.32 | -1.17 | 0.258 | 0.779 | 0.998 | 20339 | tags=52%, list=37%, signal=82% | |
1433 | REGULATION OF MICROTUBULE DEPOLYMERIZATION | 39 | -0.35 | -1.17 | 0.249 | 0.779 | 0.998 | 29029 | tags=72%, list=53%, signal=153% | |
1434 | COVALENT CHROMATIN MODIFICATION | 674 | -0.30 | -1.17 | 0.223 | 0.779 | 0.998 | 23488 | tags=56%, list=43%, signal=97% | |
1435 | NEGATIVE REGULATION OF HISTONE MODIFICATION | 78 | -0.35 | -1.17 | 0.223 | 0.779 | 0.998 | 15434 | tags=47%, list=28%, signal=66% | |
1436 | NEGATIVE REGULATION OF CHOLESTEROL STORAGE | 19 | -0.42 | -1.16 | 0.274 | 0.780 | 0.998 | 23466 | tags=74%, list=43%, signal=129% | |
1437 | ACTIN CYTOSKELETON REORGANIZATION | 130 | -0.29 | -1.16 | 0.233 | 0.779 | 0.998 | 12705 | tags=32%, list=23%, signal=41% | |
1438 | RESPONSE TO STEROID HORMONE | 258 | -0.27 | -1.16 | 0.167 | 0.780 | 0.998 | 21268 | tags=44%, list=39%, signal=71% | |
1439 | REGULATION OF SYNAPTIC PLASTICITY | 118 | -0.28 | -1.16 | 0.277 | 0.780 | 0.998 | 14025 | tags=35%, list=26%, signal=47% | |
1440 | ABSCISSION | 11 | -0.44 | -1.16 | 0.285 | 0.780 | 0.998 | 14770 | tags=55%, list=27%, signal=75% | |
1441 | PHOSPHATIDYLGLYCEROL ACYL-CHAIN REMODELING | 34 | -0.33 | -1.16 | 0.278 | 0.780 | 0.998 | 23812 | tags=59%, list=44%, signal=104% | |
1442 | NEGATIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 279 | -0.29 | -1.16 | 0.246 | 0.779 | 0.998 | 23748 | tags=53%, list=43%, signal=94% | |
1443 | POSITIVE REGULATION OF PROTEIN COMPLEX ASSEMBLY | 284 | -0.30 | -1.16 | 0.241 | 0.779 | 0.998 | 19452 | tags=46%, list=36%, signal=71% | |
1444 | POSITIVE REGULATION OF PROTEIN TYROSINE KINASE ACTIVITY | 79 | -0.30 | -1.16 | 0.217 | 0.779 | 0.998 | 15325 | tags=37%, list=28%, signal=51% | |
1445 | DISACCHARIDE METABOLIC PROCESS | 13 | -0.45 | -1.16 | 0.286 | 0.780 | 0.998 | 12887 | tags=38%, list=24%, signal=50% | |
1446 | TELOMERE MAINTENANCE VIA TELOMERE LENGTHENING | 85 | -0.34 | -1.16 | 0.275 | 0.781 | 0.998 | 19793 | tags=53%, list=36%, signal=83% | |
1447 | RESPONSE TO TEMPERATURE STIMULUS | 299 | -0.30 | -1.16 | 0.196 | 0.781 | 0.998 | 23874 | tags=58%, list=44%, signal=102% | |
1448 | T CELL RECEPTOR SIGNALING PATHWAY | 324 | -0.32 | -1.16 | 0.256 | 0.781 | 0.998 | 23257 | tags=57%, list=43%, signal=99% | |
1449 | MRNA STABILIZATION | 87 | -0.32 | -1.16 | 0.273 | 0.783 | 0.998 | 22965 | tags=56%, list=42%, signal=97% | |
1450 | FLUID TRANSPORT | 90 | -0.29 | -1.16 | 0.215 | 0.783 | 0.998 | 20922 | tags=43%, list=38%, signal=70% | |
1451 | NEGATIVE REGULATION OF RECEPTOR ACTIVITY | 82 | -0.32 | -1.16 | 0.226 | 0.784 | 0.998 | 19515 | tags=45%, list=36%, signal=70% | |
1452 | POSITIVE REGULATION OF B CELL DIFFERENTIATION | 12 | -0.42 | -1.16 | 0.284 | 0.784 | 0.998 | 4505 | tags=25%, list=8%, signal=27% | |
1453 | AMINO ACID TRANSMEMBRANE TRANSPORT | 82 | -0.31 | -1.16 | 0.278 | 0.783 | 0.998 | 20980 | tags=50%, list=38%, signal=81% | |
1454 | SULFUR AMINO ACID TRANSPORT | 13 | -0.45 | -1.16 | 0.283 | 0.783 | 0.998 | 25451 | tags=85%, list=47%, signal=158% | |
1455 | B CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 42 | -0.32 | -1.16 | 0.257 | 0.783 | 0.999 | 17597 | tags=43%, list=32%, signal=63% | |
1456 | CELLULAR RESPONSE TO RETINOIC ACID | 87 | -0.30 | -1.16 | 0.236 | 0.783 | 0.999 | 14598 | tags=36%, list=27%, signal=49% | |
1457 | MAINTENANCE OF PROTEIN LOCATION | 156 | -0.29 | -1.16 | 0.209 | 0.782 | 0.999 | 22928 | tags=52%, list=42%, signal=89% | |
1458 | DOUBLE-STRAND BREAK REPAIR | 384 | -0.32 | -1.16 | 0.195 | 0.782 | 0.999 | 27569 | tags=67%, list=50%, signal=134% | |
1459 | METHYLATION | 386 | -0.31 | -1.16 | 0.187 | 0.782 | 0.999 | 27726 | tags=64%, list=51%, signal=129% | |
1460 | MYELOID CELL HOMEOSTASIS | 97 | -0.33 | -1.16 | 0.282 | 0.782 | 0.999 | 17817 | tags=45%, list=33%, signal=67% | |
1461 | POSITIVE REGULATION OF TRIGLYCERIDE METABOLIC PROCESS | 42 | -0.34 | -1.16 | 0.299 | 0.781 | 0.999 | 16447 | tags=40%, list=30%, signal=58% | |
1462 | MODULATION BY SYMBIONT OF HOST CELLULAR PROCESS | 135 | -0.34 | -1.16 | 0.302 | 0.783 | 0.999 | 23874 | tags=61%, list=44%, signal=109% | |
1463 | ERYTHROCYTE DEVELOPMENT | 9 | -0.45 | -1.16 | 0.278 | 0.782 | 0.999 | 20931 | tags=56%, list=38%, signal=90% | |
1464 | POSITIVE REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 80 | -0.31 | -1.16 | 0.244 | 0.782 | 0.999 | 11450 | tags=30%, list=21%, signal=38% | |
1465 | NEGATIVE REGULATION OF DNA REPLICATION | 128 | -0.32 | -1.16 | 0.206 | 0.782 | 0.999 | 22965 | tags=55%, list=42%, signal=94% | |
1466 | PROTEIN ACYLATION | 319 | -0.30 | -1.16 | 0.212 | 0.783 | 0.999 | 22646 | tags=54%, list=41%, signal=91% | |
1467 | INNATE IMMUNE RESPONSE-ACTIVATING SIGNAL TRANSDUCTION | 569 | -0.32 | -1.16 | 0.271 | 0.783 | 0.999 | 21479 | tags=53%, list=39%, signal=86% | |
1468 | POSITIVE REGULATION OF PEPTIDYL-THREONINE PHOSPHORYLATION | 51 | -0.34 | -1.16 | 0.286 | 0.783 | 0.999 | 21479 | tags=55%, list=39%, signal=90% | |
1469 | REGULATION OF COLLAGEN BIOSYNTHETIC PROCESS | 23 | -0.36 | -1.16 | 0.284 | 0.782 | 0.999 | 14822 | tags=39%, list=27%, signal=54% | |
1470 | NEGATIVE REGULATION OF STEM CELL DIFFERENTIATION | 79 | -0.31 | -1.16 | 0.244 | 0.782 | 0.999 | 19530 | tags=48%, list=36%, signal=75% | |
1471 | POSITIVE REGULATION OF RECEPTOR BIOSYNTHETIC PROCESS | 20 | -0.40 | -1.16 | 0.263 | 0.783 | 0.999 | 7462 | tags=35%, list=14%, signal=41% | |
1472 | L-SERINE METABOLIC PROCESS | 22 | -0.39 | -1.16 | 0.316 | 0.783 | 0.999 | 25054 | tags=68%, list=46%, signal=126% | |
1473 | LONG-CHAIN FATTY-ACYL-COA BIOSYNTHETIC PROCESS | 82 | -0.33 | -1.16 | 0.239 | 0.782 | 0.999 | 27232 | tags=66%, list=50%, signal=131% | |
1474 | FATTY-ACYL-COA BIOSYNTHETIC PROCESS | 82 | -0.33 | -1.16 | 0.239 | 0.782 | 0.999 | 27232 | tags=66%, list=50%, signal=131% | |
1475 | BENZENE-CONTAINING COMPOUND METABOLIC PROCESS | 18 | -0.42 | -1.16 | 0.311 | 0.783 | 0.999 | 22310 | tags=72%, list=41%, signal=122% | |
1476 | ALCOHOL BIOSYNTHETIC PROCESS | 152 | -0.29 | -1.16 | 0.245 | 0.783 | 0.999 | 22797 | tags=52%, list=42%, signal=89% | |
1477 | MODULATION BY VIRUS OF HOST MORPHOLOGY OR PHYSIOLOGY | 150 | -0.34 | -1.16 | 0.280 | 0.783 | 0.999 | 23874 | tags=61%, list=44%, signal=109% | |
1478 | REGULATION OF RAS PROTEIN SIGNAL TRANSDUCTION | 154 | -0.30 | -1.16 | 0.251 | 0.783 | 0.999 | 18711 | tags=43%, list=34%, signal=65% | |
1479 | NEGATIVE REGULATION OF RNA SPLICING | 60 | -0.36 | -1.16 | 0.282 | 0.783 | 0.999 | 23769 | tags=62%, list=43%, signal=109% | |
1480 | RESPONSE TO REDOX STATE | 23 | -0.39 | -1.16 | 0.321 | 0.783 | 0.999 | 17413 | tags=52%, list=32%, signal=77% | |
1481 | REGULATION OF TRANSLATION | 535 | -0.31 | -1.16 | 0.213 | 0.785 | 0.999 | 23741 | tags=59%, list=43%, signal=102% | |
1482 | ACETYL-COA METABOLIC PROCESS | 31 | -0.37 | -1.16 | 0.310 | 0.786 | 0.999 | 22600 | tags=65%, list=41%, signal=110% | |
1483 | NEGATIVE REGULATION OF ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 99 | -0.29 | -1.16 | 0.282 | 0.785 | 0.999 | 26192 | tags=57%, list=48%, signal=108% | |
1484 | TRANSCRIPTION INITIATION FROM RNA POLYMERASE I PROMOTER | 73 | -0.34 | -1.16 | 0.307 | 0.785 | 0.999 | 25931 | tags=67%, list=47%, signal=128% | |
1485 | REGULATION OF CELLULAR AMIDE METABOLIC PROCESS | 577 | -0.31 | -1.16 | 0.228 | 0.785 | 0.999 | 23648 | tags=58%, list=43%, signal=101% | |
1486 | ENDOSOME ORGANIZATION | 101 | -0.35 | -1.15 | 0.317 | 0.785 | 0.999 | 19759 | tags=53%, list=36%, signal=84% | |
1487 | RNA SPLICING | 605 | -0.33 | -1.15 | 0.319 | 0.785 | 0.999 | 24545 | tags=61%, list=45%, signal=110% | |
1488 | CELLULAR RESPONSE TO IONIZING RADIATION | 85 | -0.34 | -1.15 | 0.299 | 0.784 | 0.999 | 19314 | tags=53%, list=35%, signal=82% | |
1489 | RHO PROTEIN SIGNAL TRANSDUCTION | 75 | -0.30 | -1.15 | 0.261 | 0.784 | 0.999 | 17808 | tags=43%, list=33%, signal=63% | |
1490 | MACROMITOPHAGY | 325 | -0.28 | -1.15 | 0.268 | 0.784 | 0.999 | 14229 | tags=36%, list=26%, signal=49% | |
1491 | PHOSPHATIDYLINOSITOL METABOLIC PROCESS | 290 | -0.31 | -1.15 | 0.150 | 0.784 | 0.999 | 27544 | tags=66%, list=50%, signal=132% | |
1492 | NEGATIVE REGULATION OF INTRACELLULAR STEROID HORMONE RECEPTOR SIGNALING PATHWAY | 89 | -0.31 | -1.15 | 0.230 | 0.783 | 0.999 | 20092 | tags=51%, list=37%, signal=80% | |
1493 | ENDOSOME TO LYSOSOME TRANSPORT | 74 | -0.33 | -1.15 | 0.288 | 0.783 | 0.999 | 28134 | tags=69%, list=51%, signal=142% | |
1494 | CELLULAR RESPONSE TO NUTRIENT LEVELS | 199 | -0.32 | -1.15 | 0.221 | 0.783 | 0.999 | 27744 | tags=68%, list=51%, signal=138% | |
1495 | REGULATION OF MITOTIC CELL CYCLE | 843 | -0.30 | -1.15 | 0.181 | 0.784 | 0.999 | 24611 | tags=57%, list=45%, signal=102% | |
1496 | REGULATION OF PROTEIN TARGETING | 546 | -0.28 | -1.15 | 0.204 | 0.783 | 0.999 | 16386 | tags=39%, list=30%, signal=55% | |
1497 | T-HELPER 1 TYPE IMMUNE RESPONSE | 20 | -0.39 | -1.15 | 0.276 | 0.783 | 0.999 | 22598 | tags=60%, list=41%, signal=102% | |
1498 | REGULATION OF CILIUM ASSEMBLY | 58 | -0.32 | -1.15 | 0.256 | 0.783 | 0.999 | 24437 | tags=60%, list=45%, signal=109% | |
1499 | RIBONUCLEOPROTEIN COMPLEX SUBUNIT ORGANIZATION | 304 | -0.33 | -1.15 | 0.290 | 0.783 | 0.999 | 24568 | tags=61%, list=45%, signal=110% | |
1500 | POSITIVE REGULATION OF MACROAUTOPHAGY | 104 | -0.35 | -1.15 | 0.288 | 0.783 | 0.999 | 25040 | tags=68%, list=46%, signal=126% | |
1501 | POSITIVE REGULATION OF INTERLEUKIN-1 SECRETION | 32 | -0.37 | -1.15 | 0.271 | 0.783 | 0.999 | 13148 | tags=41%, list=24%, signal=53% | |
1502 | GLYCOPROTEIN BIOSYNTHETIC PROCESS | 924 | -0.29 | -1.15 | 0.241 | 0.785 | 0.999 | 21261 | tags=49%, list=39%, signal=78% | |
1503 | NEGATIVE REGULATION OF ANTIGEN PROCESSING AND PRESENTATION | 33 | -0.37 | -1.15 | 0.314 | 0.785 | 0.999 | 7049 | tags=27%, list=13%, signal=31% | |
1504 | POSITIVE REGULATION OF LEUKOCYTE DEGRANULATION | 17 | -0.43 | -1.15 | 0.305 | 0.784 | 0.999 | 16673 | tags=59%, list=30%, signal=85% | |
1505 | EPIDERMAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 866 | -0.27 | -1.15 | 0.188 | 0.785 | 0.999 | 22329 | tags=48%, list=41%, signal=79% | |
1506 | NEGATIVE REGULATION OF ERAD PATHWAY | 37 | -0.37 | -1.15 | 0.309 | 0.786 | 0.999 | 15093 | tags=49%, list=28%, signal=67% | |
1507 | POSITIVE REGULATION OF DNA BIOSYNTHETIC PROCESS | 80 | -0.31 | -1.15 | 0.275 | 0.786 | 0.999 | 23219 | tags=56%, list=42%, signal=98% | |
1508 | CARTILAGE DEVELOPMENT INVOLVED IN ENDOCHONDRAL BONE MORPHOGENESIS | 9 | -0.49 | -1.15 | 0.294 | 0.785 | 0.999 | 6904 | tags=33%, list=13%, signal=38% | |
1509 | METANEPHRIC TUBULE MORPHOGENESIS | 17 | -0.40 | -1.15 | 0.298 | 0.785 | 0.999 | 17093 | tags=47%, list=31%, signal=68% | |
1510 | METANEPHRIC NEPHRON TUBULE MORPHOGENESIS | 17 | -0.40 | -1.15 | 0.298 | 0.784 | 0.999 | 17093 | tags=47%, list=31%, signal=68% | |
1511 | EPITHELIAL TUBE FORMATION | 86 | -0.31 | -1.15 | 0.281 | 0.785 | 0.999 | 17093 | tags=43%, list=31%, signal=62% | |
1512 | CYTOSKELETON-DEPENDENT CYTOKINESIS | 83 | -0.32 | -1.15 | 0.269 | 0.786 | 0.999 | 27678 | tags=67%, list=51%, signal=136% | |
1513 | SPINDLE ASSEMBLY | 101 | -0.35 | -1.15 | 0.261 | 0.787 | 0.999 | 27144 | tags=73%, list=50%, signal=145% | |
1514 | ENDOMEMBRANE SYSTEM ORGANIZATION | 842 | -0.30 | -1.15 | 0.245 | 0.787 | 0.999 | 22625 | tags=52%, list=41%, signal=88% | |
1515 | MITOCHONDRIAL TRNA PROCESSING | 10 | -0.48 | -1.15 | 0.319 | 0.787 | 0.999 | 12964 | tags=60%, list=24%, signal=79% | |
1516 | EPITHELIAL CELL-CELL ADHESION | 20 | -0.41 | -1.15 | 0.315 | 0.787 | 0.999 | 22748 | tags=70%, list=42%, signal=120% | |
1517 | POSITIVE REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 89 | -0.32 | -1.15 | 0.254 | 0.787 | 0.999 | 17823 | tags=45%, list=33%, signal=67% | |
1518 | POLYSACCHARIDE BIOSYNTHETIC PROCESS | 55 | -0.33 | -1.15 | 0.307 | 0.787 | 0.999 | 27375 | tags=65%, list=50%, signal=131% | |
1519 | CELLULAR POLYSACCHARIDE BIOSYNTHETIC PROCESS | 55 | -0.33 | -1.15 | 0.307 | 0.786 | 0.999 | 27375 | tags=65%, list=50%, signal=131% | |
1520 | CELLULAR PROTEIN COMPLEX ASSEMBLY | 557 | -0.31 | -1.15 | 0.186 | 0.786 | 0.999 | 21543 | tags=54%, list=39%, signal=88% | |
1521 | GLYCOPROTEIN METABOLIC PROCESS | 1013 | -0.28 | -1.15 | 0.249 | 0.787 | 0.999 | 21261 | tags=48%, list=39%, signal=77% | |
1522 | NEGATIVE REGULATION OF NF-KAPPAB TRANSCRIPTION FACTOR ACTIVITY | 148 | -0.29 | -1.15 | 0.241 | 0.788 | 0.999 | 29151 | tags=62%, list=53%, signal=133% | |
1523 | PYRIMIDINE-CONTAINING COMPOUND SALVAGE | 17 | -0.40 | -1.15 | 0.294 | 0.788 | 0.999 | 28039 | tags=82%, list=51%, signal=169% | |
1524 | PYRIMIDINE NUCLEOSIDE SALVAGE | 17 | -0.40 | -1.15 | 0.294 | 0.787 | 0.999 | 28039 | tags=82%, list=51%, signal=169% | |
1525 | PROTEIN METHYLATION | 205 | -0.32 | -1.15 | 0.275 | 0.787 | 0.999 | 27726 | tags=67%, list=51%, signal=136% | |
1526 | PROTEIN ALKYLATION | 205 | -0.32 | -1.15 | 0.275 | 0.787 | 0.999 | 27726 | tags=67%, list=51%, signal=136% | |
1527 | NEGATIVE REGULATION OF MICROTUBULE DEPOLYMERIZATION | 38 | -0.34 | -1.15 | 0.276 | 0.787 | 0.999 | 29029 | tags=71%, list=53%, signal=151% | |
1528 | DNA-TEMPLATED TRANSCRIPTION, TERMINATION | 222 | -0.33 | -1.15 | 0.326 | 0.786 | 0.999 | 26247 | tags=67%, list=48%, signal=129% | |
1529 | MACROAUTOPHAGY | 562 | -0.29 | -1.15 | 0.265 | 0.786 | 0.999 | 21184 | tags=50%, list=39%, signal=80% | |
1530 | DNA-TEMPLATED TRANSCRIPTION, INITIATION | 714 | -0.29 | -1.15 | 0.198 | 0.786 | 0.999 | 25983 | tags=59%, list=48%, signal=112% | |
1531 | PROTEIN LOCALIZATION TO EXTRACELLULAR REGION | 11 | -0.42 | -1.15 | 0.302 | 0.787 | 0.999 | 13378 | tags=45%, list=24%, signal=60% | |
1532 | MAINTENANCE OF PROTEIN LOCATION IN EXTRACELLULAR REGION | 11 | -0.42 | -1.15 | 0.302 | 0.787 | 0.999 | 13378 | tags=45%, list=24%, signal=60% | |
1533 | REGULATION OF CELL PROJECTION ASSEMBLY | 228 | -0.29 | -1.15 | 0.218 | 0.787 | 0.999 | 26865 | tags=58%, list=49%, signal=113% | |
1534 | CELLULAR RESPONSE TO UV | 110 | -0.32 | -1.15 | 0.284 | 0.787 | 0.999 | 18412 | tags=49%, list=34%, signal=74% | |
1535 | PLASMA MEMBRANE ORGANIZATION | 359 | -0.28 | -1.15 | 0.184 | 0.787 | 0.999 | 21400 | tags=48%, list=39%, signal=78% | |
1536 | ESTABLISHMENT OF GOLGI LOCALIZATION | 16 | -0.43 | -1.15 | 0.321 | 0.786 | 0.999 | 23805 | tags=75%, list=44%, signal=133% | |
1537 | RIBONUCLEOPROTEIN COMPLEX ASSEMBLY | 284 | -0.33 | -1.15 | 0.315 | 0.786 | 0.999 | 24568 | tags=61%, list=45%, signal=110% | |
1538 | POSITIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 489 | -0.29 | -1.15 | 0.213 | 0.786 | 0.999 | 25892 | tags=58%, list=47%, signal=109% | |
1539 | PROTEIN K27-LINKED UBIQUITINATION | 13 | -0.42 | -1.15 | 0.325 | 0.787 | 0.999 | 28674 | tags=85%, list=52%, signal=178% | |
1540 | NEGATIVE REGULATION OF BINDING | 238 | -0.29 | -1.15 | 0.210 | 0.787 | 0.999 | 16315 | tags=40%, list=30%, signal=57% | |
1541 | INTRACELLULAR STEROID HORMONE RECEPTOR SIGNALING PATHWAY | 112 | -0.30 | -1.15 | 0.201 | 0.786 | 0.999 | 21542 | tags=50%, list=39%, signal=82% | |
1542 | RESPONSE TO GROWTH HORMONE | 97 | -0.31 | -1.15 | 0.308 | 0.787 | 0.999 | 25689 | tags=57%, list=47%, signal=107% | |
1543 | REGULATION OF CELLULAR PROTEIN LOCALIZATION | 1081 | -0.29 | -1.15 | 0.156 | 0.786 | 0.999 | 25992 | tags=58%, list=48%, signal=109% | |
1544 | REGULATION OF RHO PROTEIN SIGNAL TRANSDUCTION | 78 | -0.31 | -1.15 | 0.297 | 0.787 | 0.999 | 16252 | tags=38%, list=30%, signal=55% | |
1545 | TOLL-LIKE RECEPTOR 5 SIGNALING PATHWAY | 180 | -0.32 | -1.14 | 0.295 | 0.787 | 0.999 | 25217 | tags=62%, list=46%, signal=114% | |
1546 | TOLL-LIKE RECEPTOR 10 SIGNALING PATHWAY | 180 | -0.32 | -1.14 | 0.295 | 0.786 | 0.999 | 25217 | tags=62%, list=46%, signal=114% | |
1547 | NEGATIVE REGULATION OF CILIUM ASSEMBLY | 18 | -0.41 | -1.14 | 0.307 | 0.787 | 0.999 | 9704 | tags=39%, list=18%, signal=47% | |
1548 | RESPONSE TO INACTIVITY | 13 | -0.41 | -1.14 | 0.284 | 0.788 | 0.999 | 6383 | tags=31%, list=12%, signal=35% | |
1549 | RESPONSE TO MUSCLE INACTIVITY | 13 | -0.41 | -1.14 | 0.284 | 0.788 | 0.999 | 6383 | tags=31%, list=12%, signal=35% | |
1550 | RESPONSE TO MUSCLE INACTIVITY INVOLVED IN REGULATION OF MUSCLE ADAPTATION | 13 | -0.41 | -1.14 | 0.284 | 0.787 | 0.999 | 6383 | tags=31%, list=12%, signal=35% | |
1551 | RESPONSE TO DENERVATION INVOLVED IN REGULATION OF MUSCLE ADAPTATION | 13 | -0.41 | -1.14 | 0.284 | 0.787 | 0.999 | 6383 | tags=31%, list=12%, signal=35% | |
1552 | SULFUR COMPOUND BIOSYNTHETIC PROCESS | 354 | -0.29 | -1.14 | 0.271 | 0.786 | 0.999 | 27573 | tags=62%, list=50%, signal=125% | |
1553 | MRNA 3'-SPLICE SITE RECOGNITION | 12 | -0.45 | -1.14 | 0.302 | 0.786 | 0.999 | 14083 | tags=58%, list=26%, signal=79% | |
1554 | REGULATION OF STRESS-ACTIVATED MAPK CASCADE | 337 | -0.29 | -1.14 | 0.252 | 0.786 | 0.999 | 18538 | tags=44%, list=34%, signal=66% | |
1555 | AUDITORY RECEPTOR CELL DIFFERENTIATION | 8 | -0.49 | -1.14 | 0.300 | 0.787 | 0.999 | 23342 | tags=75%, list=43%, signal=131% | |
1556 | POSITIVE REGULATION OF RECEPTOR-MEDIATED ENDOCYTOSIS | 118 | -0.30 | -1.14 | 0.281 | 0.787 | 0.999 | 7920 | tags=26%, list=14%, signal=31% | |
1557 | MICROTUBULE DEPOLYMERIZATION | 17 | -0.40 | -1.14 | 0.303 | 0.788 | 0.999 | 25722 | tags=71%, list=47%, signal=133% | |
1558 | MACROMOLECULE METHYLATION | 337 | -0.31 | -1.14 | 0.210 | 0.788 | 0.999 | 27726 | tags=64%, list=51%, signal=130% | |
1559 | REGULATION OF CYCLIN-DEPENDENT PROTEIN SERINE/THREONINE KINASE ACTIVITY INVOLVED IN G1/S TRANSITION OF MITOTIC CELL CYCLE | 33 | -0.34 | -1.14 | 0.285 | 0.789 | 0.999 | 18246 | tags=48%, list=33%, signal=73% | |
1560 | REGULATION OF ER TO GOLGI VESICLE-MEDIATED TRANSPORT | 15 | -0.42 | -1.14 | 0.336 | 0.789 | 0.999 | 10276 | tags=47%, list=19%, signal=57% | |
1561 | NEGATIVE REGULATION OF T CELL MEDIATED IMMUNITY | 30 | -0.41 | -1.14 | 0.321 | 0.788 | 0.999 | 3999 | tags=23%, list=7%, signal=25% | |
1562 | MONOCARBOXYLIC ACID METABOLIC PROCESS | 721 | -0.28 | -1.14 | 0.279 | 0.788 | 0.999 | 25746 | tags=57%, list=47%, signal=107% | |
1563 | MEMBRANE RAFT ASSEMBLY | 28 | -0.38 | -1.14 | 0.333 | 0.789 | 0.999 | 20729 | tags=61%, list=38%, signal=98% | |
1564 | CELLULAR OXIDANT DETOXIFICATION | 102 | -0.33 | -1.14 | 0.340 | 0.789 | 0.999 | 21008 | tags=52%, list=38%, signal=84% | |
1565 | POSITIVE REGULATION OF STRESS-ACTIVATED MAPK CASCADE | 202 | -0.30 | -1.14 | 0.278 | 0.789 | 0.999 | 18538 | tags=45%, list=34%, signal=67% | |
1566 | NEGATIVE REGULATION OF CELLULAR AMIDE METABOLIC PROCESS | 284 | -0.31 | -1.14 | 0.267 | 0.789 | 0.999 | 22585 | tags=55%, list=41%, signal=94% | |
1567 | AMMONIUM ION METABOLIC PROCESS | 230 | -0.28 | -1.14 | 0.264 | 0.789 | 1.000 | 26145 | tags=57%, list=48%, signal=110% | |
1568 | CELLULAR RESPONSE TO AMINO ACID STARVATION | 42 | -0.36 | -1.14 | 0.332 | 0.788 | 1.000 | 22025 | tags=62%, list=40%, signal=104% | |
1569 | REGULATION OF CELL CYCLE PROCESS | 1050 | -0.29 | -1.14 | 0.183 | 0.788 | 1.000 | 26192 | tags=58%, list=48%, signal=110% | |
1570 | ERBB SIGNALING PATHWAY | 872 | -0.27 | -1.14 | 0.200 | 0.788 | 1.000 | 22329 | tags=48%, list=41%, signal=79% | |
1571 | MRNA MODIFICATION | 27 | -0.35 | -1.14 | 0.311 | 0.789 | 1.000 | 14669 | tags=44%, list=27%, signal=61% | |
1572 | RENAL WATER HOMEOSTASIS | 89 | -0.28 | -1.14 | 0.253 | 0.789 | 1.000 | 20922 | tags=44%, list=38%, signal=71% | |
1573 | SUBSTANTIA NIGRA DEVELOPMENT | 109 | -0.33 | -1.14 | 0.319 | 0.790 | 1.000 | 22521 | tags=58%, list=41%, signal=98% | |
1574 | NEGATIVE REGULATION OF GENE EXPRESSION, EPIGENETIC | 225 | -0.32 | -1.14 | 0.248 | 0.790 | 1.000 | 21551 | tags=54%, list=39%, signal=88% | |
1575 | ALTERNATIVE MRNA SPLICING, VIA SPLICEOSOME | 40 | -0.35 | -1.14 | 0.318 | 0.789 | 1.000 | 21169 | tags=55%, list=39%, signal=90% | |
1576 | NCRNA TRANSCRIPTION | 38 | -0.35 | -1.14 | 0.294 | 0.789 | 1.000 | 16452 | tags=47%, list=30%, signal=68% | |
1577 | MODIFICATION BY SYMBIONT OF HOST MORPHOLOGY OR PHYSIOLOGY | 165 | -0.33 | -1.14 | 0.295 | 0.789 | 1.000 | 22221 | tags=57%, list=41%, signal=96% | |
1578 | TELOMERE ORGANIZATION | 178 | -0.32 | -1.14 | 0.220 | 0.789 | 1.000 | 20321 | tags=51%, list=37%, signal=81% | |
1579 | CARBOHYDRATE PHOSPHORYLATION | 35 | -0.33 | -1.14 | 0.278 | 0.788 | 1.000 | 20532 | tags=49%, list=38%, signal=78% | |
1580 | ER-NUCLEUS SIGNALING PATHWAY | 72 | -0.34 | -1.14 | 0.329 | 0.788 | 1.000 | 20833 | tags=54%, list=38%, signal=87% | |
1581 | MITOTIC NUCLEAR DIVISION | 299 | -0.33 | -1.14 | 0.285 | 0.788 | 1.000 | 21773 | tags=57%, list=40%, signal=95% | |
1582 | REGULATION OF EXTRACELLULAR EXOSOME ASSEMBLY | 8 | -0.51 | -1.14 | 0.330 | 0.788 | 1.000 | 22998 | tags=88%, list=42%, signal=151% | |
1583 | POSITIVE REGULATION OF INTERLEUKIN-1 BETA PRODUCTION | 33 | -0.37 | -1.14 | 0.304 | 0.788 | 1.000 | 13148 | tags=39%, list=24%, signal=52% | |
1584 | MRNA METHYLATION | 18 | -0.42 | -1.14 | 0.345 | 0.788 | 1.000 | 14669 | tags=56%, list=27%, signal=76% | |
1585 | ACETYL-COA BIOSYNTHETIC PROCESS FROM PYRUVATE | 11 | -0.51 | -1.14 | 0.349 | 0.788 | 1.000 | 20147 | tags=82%, list=37%, signal=130% | |
1586 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 27 | -0.37 | -1.14 | 0.307 | 0.787 | 1.000 | 20293 | tags=52%, list=37%, signal=82% | |
1587 | REGULATION OF DNA BIOSYNTHETIC PROCESS | 139 | -0.28 | -1.14 | 0.269 | 0.787 | 1.000 | 22721 | tags=50%, list=42%, signal=86% | |
1588 | CHROMATIN SILENCING | 77 | -0.31 | -1.14 | 0.280 | 0.787 | 1.000 | 28257 | tags=65%, list=52%, signal=134% | |
1589 | ORGANIC ACID TRANSMEMBRANE TRANSPORT | 169 | -0.29 | -1.14 | 0.283 | 0.786 | 1.000 | 24633 | tags=55%, list=45%, signal=100% | |
1590 | MACROMOLECULE DEACYLATION | 93 | -0.29 | -1.14 | 0.289 | 0.786 | 1.000 | 23455 | tags=54%, list=43%, signal=94% | |
1591 | RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 35 | -0.38 | -1.14 | 0.342 | 0.786 | 1.000 | 20347 | tags=57%, list=37%, signal=91% | |
1592 | SPHINGOSINE METABOLIC PROCESS | 13 | -0.42 | -1.14 | 0.336 | 0.786 | 1.000 | 11350 | tags=46%, list=21%, signal=58% | |
1593 | DIOL METABOLIC PROCESS | 13 | -0.42 | -1.14 | 0.336 | 0.785 | 1.000 | 11350 | tags=46%, list=21%, signal=58% | |
1594 | HISTONE H3-K36 DEMETHYLATION | 10 | -0.43 | -1.14 | 0.293 | 0.785 | 1.000 | 21069 | tags=60%, list=39%, signal=98% | |
1595 | CELLULAR RESPONSE TO ABIOTIC STIMULUS | 433 | -0.29 | -1.14 | 0.229 | 0.785 | 1.000 | 19314 | tags=46%, list=35%, signal=71% | |
1596 | INNER EAR RECEPTOR CELL DEVELOPMENT | 7 | -0.53 | -1.14 | 0.308 | 0.785 | 1.000 | 23342 | tags=86%, list=43%, signal=150% | |
1597 | POSITIVE REGULATION OF MEMBRANE POTENTIAL | 13 | -0.44 | -1.14 | 0.280 | 0.785 | 1.000 | 25853 | tags=85%, list=47%, signal=160% | |
1598 | PROTEIN LOCALIZATION TO GOLGI APPARATUS | 43 | -0.32 | -1.14 | 0.308 | 0.784 | 1.000 | 22249 | tags=56%, list=41%, signal=94% | |
1599 | PHOSPHATIDYLINOSITOL PHOSPHORYLATION | 76 | -0.33 | -1.14 | 0.284 | 0.784 | 1.000 | 14342 | tags=39%, list=26%, signal=53% | |
1600 | BROWN FAT CELL DIFFERENTIATION | 10 | -0.45 | -1.14 | 0.327 | 0.784 | 1.000 | 8980 | tags=30%, list=16%, signal=36% | |
1601 | HOMEOSTASIS OF NUMBER OF CELLS | 130 | -0.32 | -1.14 | 0.305 | 0.784 | 1.000 | 21279 | tags=51%, list=39%, signal=83% | |
1602 | GLYCOPROTEIN CATABOLIC PROCESS | 28 | -0.32 | -1.14 | 0.273 | 0.783 | 1.000 | 16491 | tags=46%, list=30%, signal=66% | |
1603 | PEPTIDYL-GLUTAMIC ACID CARBOXYLATION | 20 | -0.39 | -1.14 | 0.346 | 0.784 | 1.000 | 16542 | tags=55%, list=30%, signal=79% | |
1604 | PROTEIN CARBOXYLATION | 20 | -0.39 | -1.14 | 0.346 | 0.783 | 1.000 | 16542 | tags=55%, list=30%, signal=79% | |
1605 | POLYOL METABOLIC PROCESS | 154 | -0.29 | -1.14 | 0.262 | 0.783 | 1.000 | 23100 | tags=53%, list=42%, signal=92% | |
1606 | NEGATIVE REGULATION OF FATTY ACID BIOSYNTHETIC PROCESS | 18 | -0.37 | -1.14 | 0.321 | 0.782 | 1.000 | 19183 | tags=56%, list=35%, signal=86% | |
1607 | VACUOLAR TRANSPORT | 137 | -0.32 | -1.14 | 0.277 | 0.783 | 1.000 | 25826 | tags=61%, list=47%, signal=116% | |
1608 | INTRACELLULAR LIPID TRANSPORT | 51 | -0.35 | -1.14 | 0.314 | 0.783 | 1.000 | 22600 | tags=61%, list=41%, signal=104% | |
1609 | NEGATIVE REGULATION OF PRI-MIRNA TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 25 | -0.38 | -1.14 | 0.281 | 0.783 | 1.000 | 24508 | tags=68%, list=45%, signal=123% | |
1610 | POSITIVE REGULATION OF NF-KAPPAB TRANSCRIPTION FACTOR ACTIVITY | 287 | -0.30 | -1.14 | 0.344 | 0.783 | 1.000 | 23814 | tags=55%, list=44%, signal=98% | |
1611 | GTP METABOLIC PROCESS | 16 | -0.46 | -1.14 | 0.334 | 0.783 | 1.000 | 27261 | tags=94%, list=50%, signal=187% | |
1612 | POSITIVE REGULATION OF CELL CYCLE | 652 | -0.28 | -1.14 | 0.191 | 0.783 | 1.000 | 25186 | tags=54%, list=46%, signal=99% | |
1613 | REGULATION OF TELOMERE CAPPING | 64 | -0.32 | -1.14 | 0.297 | 0.784 | 1.000 | 16235 | tags=41%, list=30%, signal=58% | |
1614 | NEGATIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 150 | -0.32 | -1.14 | 0.314 | 0.784 | 1.000 | 19445 | tags=49%, list=36%, signal=76% | |
1615 | CHROMATIN ASSEMBLY OR DISASSEMBLY | 221 | -0.30 | -1.13 | 0.216 | 0.784 | 1.000 | 19966 | tags=48%, list=37%, signal=75% | |
1616 | NEGATIVE REGULATION OF RECEPTOR-MEDIATED ENDOCYTOSIS | 38 | -0.36 | -1.13 | 0.326 | 0.784 | 1.000 | 16495 | tags=50%, list=30%, signal=72% | |
1617 | C-5 METHYLATION OF CYTOSINE | 7 | -0.48 | -1.13 | 0.306 | 0.784 | 1.000 | 5692 | tags=43%, list=10%, signal=48% | |
1618 | PROTEIN MATURATION | 443 | -0.29 | -1.13 | 0.276 | 0.783 | 1.000 | 24004 | tags=55%, list=44%, signal=98% | |
1619 | CYTOKINETIC PROCESS | 25 | -0.34 | -1.13 | 0.300 | 0.783 | 1.000 | 18728 | tags=52%, list=34%, signal=79% | |
1620 | REGULATION OF EXTRACELLULAR MATRIX DISASSEMBLY | 34 | -0.33 | -1.13 | 0.282 | 0.783 | 1.000 | 18901 | tags=44%, list=35%, signal=67% | |
1621 | GOLGI TO PLASMA MEMBRANE TRANSPORT | 87 | -0.32 | -1.13 | 0.317 | 0.783 | 1.000 | 25853 | tags=62%, list=47%, signal=118% | |
1622 | POSITIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 708 | -0.29 | -1.13 | 0.196 | 0.783 | 1.000 | 26162 | tags=58%, list=48%, signal=110% | |
1623 | TOLL-LIKE RECEPTOR 3 SIGNALING PATHWAY | 211 | -0.32 | -1.13 | 0.323 | 0.782 | 1.000 | 18444 | tags=47%, list=34%, signal=71% | |
1624 | OXIDATIVE PHOSPHORYLATION | 20 | -0.41 | -1.13 | 0.347 | 0.783 | 1.000 | 25742 | tags=80%, list=47%, signal=151% | |
1625 | POSITIVE REGULATION OF DEFENSE RESPONSE | 761 | -0.30 | -1.13 | 0.344 | 0.783 | 1.000 | 21485 | tags=50%, list=39%, signal=81% | |
1626 | PROTECTION FROM NATURAL KILLER CELL MEDIATED CYTOTOXICITY | 13 | -0.50 | -1.13 | 0.323 | 0.783 | 1.000 | 13927 | tags=62%, list=25%, signal=83% | |
1627 | PROTEIN LOCALIZATION TO NUCLEUS | 276 | -0.31 | -1.13 | 0.279 | 0.782 | 1.000 | 22430 | tags=54%, list=41%, signal=92% | |
1628 | C-TERMINAL PROTEIN AMINO ACID MODIFICATION | 70 | -0.35 | -1.13 | 0.295 | 0.782 | 1.000 | 22240 | tags=63%, list=41%, signal=106% | |
1629 | CELLULAR RESPONSE TO PROSTAGLANDIN E STIMULUS | 26 | -0.38 | -1.13 | 0.317 | 0.783 | 1.000 | 13452 | tags=42%, list=25%, signal=56% | |
1630 | NEGATIVE REGULATION OF HOMEOSTATIC PROCESS | 217 | -0.28 | -1.13 | 0.228 | 0.783 | 1.000 | 19751 | tags=43%, list=36%, signal=67% | |
1631 | NEGATIVE REGULATION OF MITOCHONDRIAL FUSION | 9 | -0.45 | -1.13 | 0.337 | 0.783 | 1.000 | 28674 | tags=89%, list=52%, signal=187% | |
1632 | SERINE FAMILY AMINO ACID BIOSYNTHETIC PROCESS | 28 | -0.37 | -1.13 | 0.346 | 0.783 | 1.000 | 26219 | tags=71%, list=48%, signal=137% | |
1633 | ACTIVATION OF ANAPHASE-PROMOTING COMPLEX ACTIVITY | 25 | -0.41 | -1.13 | 0.353 | 0.782 | 1.000 | 19973 | tags=64%, list=37%, signal=101% | |
1634 | LONG-TERM MEMORY | 18 | -0.39 | -1.13 | 0.325 | 0.782 | 1.000 | 11397 | tags=39%, list=21%, signal=49% | |
1635 | POSITIVE REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 86 | -0.31 | -1.13 | 0.307 | 0.781 | 1.000 | 23725 | tags=53%, list=43%, signal=94% | |
1636 | CELLULAR RESPONSE TO STARVATION | 164 | -0.33 | -1.13 | 0.270 | 0.781 | 1.000 | 27744 | tags=69%, list=51%, signal=139% | |
1637 | NEGATIVE REGULATION OF JNK CASCADE | 71 | -0.34 | -1.13 | 0.345 | 0.781 | 1.000 | 21267 | tags=54%, list=39%, signal=87% | |
1638 | REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE BY P53 CLASS MEDIATOR | 26 | -0.41 | -1.13 | 0.368 | 0.781 | 1.000 | 20622 | tags=65%, list=38%, signal=105% | |
1639 | NEGATIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE BY P53 CLASS MEDIATOR | 26 | -0.41 | -1.13 | 0.368 | 0.780 | 1.000 | 20622 | tags=65%, list=38%, signal=105% | |
1640 | REGULATION OF PSEUDOPODIUM ASSEMBLY | 26 | -0.36 | -1.13 | 0.318 | 0.781 | 1.000 | 29206 | tags=73%, list=53%, signal=157% | |
1641 | POSITIVE REGULATION OF PSEUDOPODIUM ASSEMBLY | 26 | -0.36 | -1.13 | 0.318 | 0.780 | 1.000 | 29206 | tags=73%, list=53%, signal=157% | |
1642 | DOUBLE-STRAND BREAK REPAIR VIA HOMOLOGOUS RECOMBINATION | 276 | -0.32 | -1.13 | 0.224 | 0.780 | 1.000 | 28383 | tags=68%, list=52%, signal=142% | |
1643 | RECOMBINATIONAL REPAIR | 276 | -0.32 | -1.13 | 0.224 | 0.780 | 1.000 | 28383 | tags=68%, list=52%, signal=142% | |
1644 | NEGATIVE REGULATION OF ORGANELLE ORGANIZATION | 584 | -0.29 | -1.13 | 0.182 | 0.780 | 1.000 | 19855 | tags=47%, list=36%, signal=73% | |
1645 | CELLULAR RESPONSE TO ACIDIC PH | 15 | -0.40 | -1.13 | 0.321 | 0.779 | 1.000 | 22671 | tags=67%, list=41%, signal=114% | |
1646 | SMALL MOLECULE BIOSYNTHETIC PROCESS | 607 | -0.27 | -1.13 | 0.290 | 0.780 | 1.000 | 27485 | tags=59%, list=50%, signal=117% | |
1647 | SISTER CHROMATID SEGREGATION | 176 | -0.32 | -1.13 | 0.312 | 0.780 | 1.000 | 21773 | tags=56%, list=40%, signal=92% | |
1648 | REGULATION OF STRESS-ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 340 | -0.29 | -1.13 | 0.282 | 0.780 | 1.000 | 18538 | tags=44%, list=34%, signal=66% | |
1649 | CELL-TYPE SPECIFIC APOPTOTIC PROCESS | 108 | -0.29 | -1.13 | 0.292 | 0.779 | 1.000 | 17275 | tags=41%, list=32%, signal=59% | |
1650 | REGULATION OF MITOTIC SISTER CHROMATID SEGREGATION | 154 | -0.34 | -1.13 | 0.361 | 0.779 | 1.000 | 24486 | tags=62%, list=45%, signal=113% | |
1651 | NCRNA CATABOLIC PROCESS | 33 | -0.38 | -1.13 | 0.352 | 0.779 | 1.000 | 29795 | tags=85%, list=54%, signal=186% | |
1652 | HEPARAN SULFATE PROTEOGLYCAN BIOSYNTHETIC PROCESS | 14 | -0.42 | -1.13 | 0.341 | 0.779 | 1.000 | 9106 | tags=43%, list=17%, signal=51% | |
1653 | POSITIVE REGULATION OF PROTEIN HOMOOLIGOMERIZATION | 19 | -0.42 | -1.13 | 0.347 | 0.779 | 1.000 | 25775 | tags=79%, list=47%, signal=149% | |
1654 | POSITIVE REGULATION OF MITOCHONDRIAL FISSION | 28 | -0.37 | -1.13 | 0.329 | 0.779 | 1.000 | 28930 | tags=79%, list=53%, signal=167% | |
1655 | REGULATION OF INTERFERON-BETA PRODUCTION | 77 | -0.36 | -1.13 | 0.350 | 0.778 | 1.000 | 17938 | tags=51%, list=33%, signal=75% | |
1656 | CELL FATE COMMITMENT INVOLVED IN FORMATION OF PRIMARY GERM LAYER | 29 | -0.34 | -1.13 | 0.284 | 0.778 | 1.000 | 21259 | tags=55%, list=39%, signal=90% | |
1657 | TUBE FORMATION | 106 | -0.30 | -1.13 | 0.284 | 0.778 | 1.000 | 11290 | tags=32%, list=21%, signal=40% | |
1658 | LEUKOTRIENE BIOSYNTHETIC PROCESS | 24 | -0.39 | -1.13 | 0.358 | 0.778 | 1.000 | 23003 | tags=67%, list=42%, signal=115% | |
1659 | DNA DOUBLE-STRAND BREAK PROCESSING INVOLVED IN REPAIR VIA SINGLE-STRAND ANNEALING | 12 | -0.41 | -1.13 | 0.337 | 0.778 | 1.000 | 26060 | tags=67%, list=48%, signal=127% | |
1660 | DOUBLE-STRAND BREAK REPAIR VIA SINGLE-STRAND ANNEALING | 12 | -0.41 | -1.13 | 0.337 | 0.778 | 1.000 | 26060 | tags=67%, list=48%, signal=127% | |
1661 | PEPTIDYL-ARGININE N-METHYLATION | 19 | -0.41 | -1.13 | 0.339 | 0.778 | 1.000 | 26114 | tags=84%, list=48%, signal=161% | |
1662 | KINETOCHORE ORGANIZATION | 9 | -0.44 | -1.13 | 0.319 | 0.778 | 1.000 | 16669 | tags=56%, list=30%, signal=80% | |
1663 | REGULATION OF HISTONE MODIFICATION | 238 | -0.30 | -1.13 | 0.256 | 0.781 | 1.000 | 16831 | tags=43%, list=31%, signal=62% | |
1664 | TISSUE REMODELING | 75 | -0.29 | -1.13 | 0.261 | 0.781 | 1.000 | 18905 | tags=41%, list=35%, signal=63% | |
1665 | REGULATION OF SEQUENCE-SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 771 | -0.27 | -1.13 | 0.294 | 0.781 | 1.000 | 23888 | tags=52%, list=44%, signal=90% | |
1666 | PROTEIN TRIMERIZATION | 58 | -0.31 | -1.13 | 0.298 | 0.781 | 1.000 | 20193 | tags=47%, list=37%, signal=74% | |
1667 | ASPARTATE FAMILY AMINO ACID METABOLIC PROCESS | 66 | -0.33 | -1.13 | 0.291 | 0.781 | 1.000 | 27903 | tags=71%, list=51%, signal=145% | |
1668 | ERYTHROCYTE HOMEOSTASIS | 85 | -0.32 | -1.13 | 0.312 | 0.781 | 1.000 | 21279 | tags=51%, list=39%, signal=83% | |
1669 | REGULATION OF INTERLEUKIN-5 PRODUCTION | 24 | -0.36 | -1.13 | 0.305 | 0.781 | 1.000 | 20339 | tags=46%, list=37%, signal=73% | |
1670 | REGULATION OF FATTY ACID BETA-OXIDATION | 43 | -0.33 | -1.13 | 0.325 | 0.782 | 1.000 | 12176 | tags=37%, list=22%, signal=48% | |
1671 | MRNA CLEAVAGE | 18 | -0.42 | -1.13 | 0.348 | 0.783 | 1.000 | 16007 | tags=61%, list=29%, signal=86% | |
1672 | TOLL-LIKE RECEPTOR 9 SIGNALING PATHWAY | 198 | -0.31 | -1.13 | 0.299 | 0.782 | 1.000 | 25217 | tags=60%, list=46%, signal=111% | |
1673 | POSITIVE REGULATION OF HISTONE UBIQUITINATION | 9 | -0.46 | -1.13 | 0.340 | 0.782 | 1.000 | 19323 | tags=56%, list=35%, signal=86% | |
1674 | RESPONSE TO GAMMA RADIATION | 43 | -0.36 | -1.13 | 0.307 | 0.782 | 1.000 | 17185 | tags=51%, list=31%, signal=75% | |
1675 | MITOTIC CYTOKINESIS | 65 | -0.32 | -1.13 | 0.310 | 0.781 | 1.000 | 25853 | tags=63%, list=47%, signal=120% | |
1676 | CYTOKINE-MEDIATED SIGNALING PATHWAY | 907 | -0.29 | -1.13 | 0.290 | 0.781 | 1.000 | 24273 | tags=54%, list=44%, signal=96% | |
1677 | POSITIVE REGULATION OF PEPTIDASE ACTIVITY | 317 | -0.31 | -1.13 | 0.346 | 0.782 | 1.000 | 18903 | tags=48%, list=35%, signal=73% | |
1678 | DNA METHYLATION OR DEMETHYLATION | 123 | -0.29 | -1.13 | 0.286 | 0.782 | 1.000 | 23465 | tags=50%, list=43%, signal=88% | |
1679 | NEGATIVE REGULATION OF STRESS FIBER ASSEMBLY | 38 | -0.32 | -1.13 | 0.299 | 0.781 | 1.000 | 18901 | tags=47%, list=35%, signal=72% | |
1680 | POSITIVE REGULATION OF MICROTUBULE POLYMERIZATION | 28 | -0.34 | -1.13 | 0.302 | 0.781 | 1.000 | 12208 | tags=36%, list=22%, signal=46% | |
1681 | RESPONSE TO GLUCOSE | 94 | -0.29 | -1.13 | 0.311 | 0.781 | 1.000 | 17426 | tags=43%, list=32%, signal=62% | |
1682 | REGULATION OF ORGANELLE ASSEMBLY | 243 | -0.31 | -1.13 | 0.295 | 0.782 | 1.000 | 26174 | tags=63%, list=48%, signal=119% | |
1683 | TRANSLESION SYNTHESIS | 98 | -0.34 | -1.13 | 0.346 | 0.781 | 1.000 | 17205 | tags=50%, list=31%, signal=73% | |
1684 | ASPARTATE FAMILY AMINO ACID CATABOLIC PROCESS | 30 | -0.36 | -1.13 | 0.327 | 0.781 | 1.000 | 21924 | tags=63%, list=40%, signal=106% | |
1685 | CHROMATIN MODIFICATION | 881 | -0.29 | -1.13 | 0.278 | 0.781 | 1.000 | 23006 | tags=54%, list=42%, signal=91% | |
1686 | SULFUR COMPOUND METABOLIC PROCESS | 579 | -0.27 | -1.13 | 0.289 | 0.781 | 1.000 | 24487 | tags=54%, list=45%, signal=97% | |
1687 | REGULATION OF TOLERANCE INDUCTION | 26 | -0.38 | -1.13 | 0.328 | 0.781 | 1.000 | 16824 | tags=54%, list=31%, signal=78% | |
1688 | REGULATION OF PROTEIN TYROSINE KINASE ACTIVITY | 122 | -0.28 | -1.13 | 0.285 | 0.780 | 1.000 | 28037 | tags=61%, list=51%, signal=124% | |
1689 | POSITIVE REGULATION OF STEROL TRANSPORT | 28 | -0.34 | -1.13 | 0.293 | 0.780 | 1.000 | 15149 | tags=39%, list=28%, signal=54% | |
1690 | POSITIVE REGULATION OF CHOLESTEROL TRANSPORT | 28 | -0.34 | -1.13 | 0.293 | 0.780 | 1.000 | 15149 | tags=39%, list=28%, signal=54% | |
1691 | RAS PROTEIN SIGNAL TRANSDUCTION | 712 | -0.25 | -1.13 | 0.278 | 0.780 | 1.000 | 22198 | tags=46%, list=41%, signal=76% | |
1692 | MANGANESE ION TRANSMEMBRANE TRANSPORT | 16 | -0.40 | -1.13 | 0.339 | 0.780 | 1.000 | 10141 | tags=44%, list=19%, signal=54% | |
1693 | ORGANELLE DISASSEMBLY | 381 | -0.28 | -1.12 | 0.308 | 0.779 | 1.000 | 14229 | tags=36%, list=26%, signal=49% | |
1694 | REGULATION OF BETA-AMYLOID FORMATION | 24 | -0.38 | -1.12 | 0.350 | 0.779 | 1.000 | 14157 | tags=46%, list=26%, signal=62% | |
1695 | POSITIVE REGULATION OF ENDOPEPTIDASE ACTIVITY | 306 | -0.31 | -1.12 | 0.366 | 0.779 | 1.000 | 18903 | tags=48%, list=35%, signal=73% | |
1696 | POSITIVE REGULATION OF TOLL-LIKE RECEPTOR SIGNALING PATHWAY | 37 | -0.35 | -1.12 | 0.307 | 0.779 | 1.000 | 19428 | tags=51%, list=36%, signal=80% | |
1697 | NEGATIVE REGULATION OF DEVELOPMENTAL GROWTH | 83 | -0.29 | -1.12 | 0.288 | 0.778 | 1.000 | 28908 | tags=61%, list=53%, signal=130% | |
1698 | JNK CASCADE | 142 | -0.31 | -1.12 | 0.290 | 0.778 | 1.000 | 25823 | tags=61%, list=47%, signal=114% | |
1699 | CELLULAR RESPONSE TO EXTRACELLULAR STIMULUS | 210 | -0.31 | -1.12 | 0.275 | 0.778 | 1.000 | 22217 | tags=55%, list=41%, signal=92% | |
1700 | DNA ALKYLATION | 102 | -0.29 | -1.12 | 0.289 | 0.778 | 1.000 | 23465 | tags=50%, list=43%, signal=87% | |
1701 | DNA METHYLATION | 102 | -0.29 | -1.12 | 0.289 | 0.778 | 1.000 | 23465 | tags=50%, list=43%, signal=87% | |
1702 | POSITIVE REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 80 | -0.34 | -1.12 | 0.298 | 0.777 | 1.000 | 21147 | tags=52%, list=39%, signal=85% | |
1703 | PROTEIN LOCALIZATION TO LYSOSOME | 46 | -0.36 | -1.12 | 0.341 | 0.778 | 1.000 | 13729 | tags=43%, list=25%, signal=58% | |
1704 | COFACTOR TRANSPORT | 39 | -0.31 | -1.12 | 0.296 | 0.778 | 1.000 | 28921 | tags=59%, list=53%, signal=125% | |
1705 | REGULATION OF CHROMOSOME ORGANIZATION | 599 | -0.30 | -1.12 | 0.222 | 0.777 | 1.000 | 23751 | tags=55%, list=43%, signal=96% | |
1706 | NEGATIVE REGULATION OF KERATINOCYTE PROLIFERATION | 21 | -0.38 | -1.12 | 0.326 | 0.777 | 1.000 | 20747 | tags=62%, list=38%, signal=100% | |
1707 | PLACENTA BLOOD VESSEL DEVELOPMENT | 17 | -0.41 | -1.12 | 0.343 | 0.777 | 1.000 | 25953 | tags=76%, list=47%, signal=146% | |
1708 | HISTONE H2A MONOUBIQUITINATION | 27 | -0.41 | -1.12 | 0.353 | 0.777 | 1.000 | 23276 | tags=74%, list=43%, signal=129% | |
1709 | POSITIVE REGULATION OF CELL CYCLE PROCESS | 475 | -0.29 | -1.12 | 0.184 | 0.776 | 1.000 | 25045 | tags=56%, list=46%, signal=103% | |
1710 | REGENERATION | 46 | -0.35 | -1.12 | 0.353 | 0.776 | 1.000 | 18711 | tags=50%, list=34%, signal=76% | |
1711 | REGULATION OF LEUKOCYTE APOPTOTIC PROCESS | 92 | -0.32 | -1.12 | 0.310 | 0.776 | 1.000 | 27777 | tags=65%, list=51%, signal=132% | |
1712 | NEGATIVE REGULATION OF MRNA SPLICING, VIA SPLICEOSOME | 49 | -0.35 | -1.12 | 0.318 | 0.775 | 1.000 | 23769 | tags=59%, list=43%, signal=105% | |
1713 | TELOMERE MAINTENANCE | 156 | -0.32 | -1.12 | 0.251 | 0.776 | 1.000 | 20321 | tags=53%, list=37%, signal=83% | |
1714 | REGULATION OF CHOLESTEROL BIOSYNTHETIC PROCESS | 15 | -0.42 | -1.12 | 0.346 | 0.776 | 1.000 | 17857 | tags=60%, list=33%, signal=89% | |
1715 | HIGH-DENSITY LIPOPROTEIN PARTICLE CLEARANCE | 16 | -0.43 | -1.12 | 0.347 | 0.775 | 1.000 | 15941 | tags=44%, list=29%, signal=62% | |
1716 | NEGATIVE REGULATION OF MYELOID CELL APOPTOTIC PROCESS | 8 | -0.44 | -1.12 | 0.324 | 0.775 | 1.000 | 12564 | tags=50%, list=23%, signal=65% | |
1717 | NEGATIVE REGULATION OF BMP SIGNALING PATHWAY | 48 | -0.31 | -1.12 | 0.285 | 0.775 | 1.000 | 11990 | tags=29%, list=22%, signal=37% | |
1718 | NEGATIVE REGULATION OF FATTY ACID OXIDATION | 17 | -0.39 | -1.12 | 0.334 | 0.774 | 1.000 | 15044 | tags=47%, list=28%, signal=65% | |
1719 | NEGATIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 150 | -0.30 | -1.12 | 0.305 | 0.774 | 1.000 | 20480 | tags=51%, list=37%, signal=81% | |
1720 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 150 | -0.30 | -1.12 | 0.305 | 0.774 | 1.000 | 20480 | tags=51%, list=37%, signal=81% | |
1721 | PROTEIN TARGETING TO PLASMA MEMBRANE | 58 | -0.30 | -1.12 | 0.303 | 0.773 | 1.000 | 8549 | tags=26%, list=16%, signal=31% | |
1722 | CHROMOSOME SEGREGATION | 305 | -0.30 | -1.12 | 0.244 | 0.773 | 1.000 | 22088 | tags=52%, list=40%, signal=87% | |
1723 | POSITIVE REGULATION OF STRESS-ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 205 | -0.29 | -1.12 | 0.314 | 0.773 | 1.000 | 18538 | tags=44%, list=34%, signal=67% | |
1724 | REGULATION OF GLYCOGEN (STARCH) SYNTHASE ACTIVITY | 16 | -0.38 | -1.12 | 0.331 | 0.774 | 1.000 | 19886 | tags=50%, list=36%, signal=79% | |
1725 | DIOL BIOSYNTHETIC PROCESS | 11 | -0.44 | -1.12 | 0.350 | 0.773 | 1.000 | 11350 | tags=45%, list=21%, signal=57% | |
1726 | SPHINGOSINE BIOSYNTHETIC PROCESS | 11 | -0.44 | -1.12 | 0.350 | 0.773 | 1.000 | 11350 | tags=45%, list=21%, signal=57% | |
1727 | NEGATIVE REGULATION OF ION TRANSMEMBRANE TRANSPORT | 129 | -0.28 | -1.12 | 0.305 | 0.773 | 1.000 | 16488 | tags=39%, list=30%, signal=55% | |
1728 | POSITIVE REGULATION OF MUSCLE CONTRACTION | 31 | -0.37 | -1.12 | 0.336 | 0.775 | 1.000 | 15903 | tags=39%, list=29%, signal=55% | |
1729 | NEGATIVE REGULATION OF OXIDATIVE STRESS-INDUCED NEURON INTRINSIC APOPTOTIC SIGNALING PATHWAY | 10 | -0.44 | -1.12 | 0.338 | 0.774 | 1.000 | 6843 | tags=40%, list=13%, signal=46% | |
1730 | ONE-CARBON METABOLIC PROCESS | 19 | -0.41 | -1.12 | 0.332 | 0.774 | 1.000 | 26219 | tags=74%, list=48%, signal=142% | |
1731 | POSITIVE REGULATION OF VIRAL ENTRY INTO HOST CELL | 15 | -0.44 | -1.12 | 0.343 | 0.774 | 1.000 | 20777 | tags=73%, list=38%, signal=118% | |
1732 | SODIUM ION EXPORT FROM CELL | 12 | -0.43 | -1.12 | 0.363 | 0.774 | 1.000 | 16903 | tags=58%, list=31%, signal=84% | |
1733 | CREATINE METABOLIC PROCESS | 25 | -0.38 | -1.12 | 0.344 | 0.773 | 1.000 | 14575 | tags=44%, list=27%, signal=60% | |
1734 | REGULATION OF EARLY ENDOSOME TO LATE ENDOSOME TRANSPORT | 54 | -0.32 | -1.12 | 0.331 | 0.773 | 1.000 | 28707 | tags=65%, list=53%, signal=136% | |
1735 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO OXIDATIVE STRESS | 15 | -0.42 | -1.12 | 0.368 | 0.773 | 1.000 | 21312 | tags=60%, list=39%, signal=98% | |
1736 | NEGATIVE REGULATION OF HISTONE ACETYLATION | 30 | -0.38 | -1.12 | 0.307 | 0.773 | 1.000 | 15434 | tags=50%, list=28%, signal=70% | |
1737 | PIGMENT BIOSYNTHETIC PROCESS | 60 | -0.32 | -1.12 | 0.340 | 0.774 | 1.000 | 20481 | tags=50%, list=37%, signal=80% | |
1738 | PROTEIN PROCESSING | 416 | -0.29 | -1.12 | 0.305 | 0.774 | 1.000 | 24004 | tags=55%, list=44%, signal=97% | |
1739 | PROTEIN LOCALIZATION TO VACUOLE | 52 | -0.35 | -1.12 | 0.359 | 0.774 | 1.000 | 23750 | tags=62%, list=43%, signal=109% | |
1740 | POSITIVE REGULATION OF RESPONSE TO CYTOKINE STIMULUS | 37 | -0.32 | -1.12 | 0.304 | 0.774 | 1.000 | 28674 | tags=68%, list=52%, signal=142% | |
1741 | CELL CYCLE ARREST | 310 | -0.29 | -1.12 | 0.315 | 0.775 | 1.000 | 24476 | tags=57%, list=45%, signal=102% | |
1742 | PROTEIN IMPORT | 250 | -0.32 | -1.12 | 0.303 | 0.775 | 1.000 | 20719 | tags=52%, list=38%, signal=84% | |
1743 | IRON ION TRANSMEMBRANE TRANSPORT | 10 | -0.41 | -1.12 | 0.309 | 0.775 | 1.000 | 14547 | tags=40%, list=27%, signal=54% | |
1744 | MYD88-INDEPENDENT TOLL-LIKE RECEPTOR SIGNALING PATHWAY | 210 | -0.31 | -1.12 | 0.334 | 0.775 | 1.000 | 18444 | tags=47%, list=34%, signal=70% | |
1745 | NEUROTROPHIN TRK RECEPTOR SIGNALING PATHWAY | 1104 | -0.26 | -1.12 | 0.227 | 0.774 | 1.000 | 26927 | tags=56%, list=49%, signal=107% | |
1746 | NEGATIVE REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 48 | -0.32 | -1.12 | 0.314 | 0.775 | 1.000 | 11102 | tags=33%, list=20%, signal=42% | |
1747 | REGULATION OF RESPONSE TO BIOTIC STIMULUS | 466 | -0.28 | -1.12 | 0.307 | 0.775 | 1.000 | 21314 | tags=48%, list=39%, signal=77% | |
1748 | POSITIVE REGULATION OF T CELL CYTOKINE PRODUCTION | 28 | -0.35 | -1.12 | 0.307 | 0.776 | 1.000 | 7829 | tags=29%, list=14%, signal=33% | |
1749 | G-PROTEIN COUPLED RECEPTOR INTERNALIZATION | 17 | -0.39 | -1.12 | 0.329 | 0.775 | 1.000 | 22116 | tags=47%, list=40%, signal=79% | |
1750 | NUCLEOSIDE SALVAGE | 19 | -0.38 | -1.12 | 0.337 | 0.775 | 1.000 | 28039 | tags=79%, list=51%, signal=162% | |
1751 | SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 37 | -0.34 | -1.12 | 0.352 | 0.776 | 1.000 | 22028 | tags=54%, list=40%, signal=90% | |
1752 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 37 | -0.34 | -1.12 | 0.352 | 0.775 | 1.000 | 22028 | tags=54%, list=40%, signal=90% | |
1753 | NEURAL TUBE DEVELOPMENT | 96 | -0.30 | -1.12 | 0.322 | 0.775 | 1.000 | 14059 | tags=38%, list=26%, signal=50% | |
1754 | POSITIVE REGULATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY | 282 | -0.31 | -1.12 | 0.359 | 0.775 | 1.000 | 21279 | tags=52%, list=39%, signal=85% | |
1755 | CELLULAR MACROMOLECULAR COMPLEX ASSEMBLY | 995 | -0.30 | -1.12 | 0.271 | 0.775 | 1.000 | 21543 | tags=52%, list=39%, signal=85% | |
1756 | RESPONSE TO STARVATION | 174 | -0.32 | -1.12 | 0.291 | 0.775 | 1.000 | 27744 | tags=68%, list=51%, signal=138% | |
1757 | DETERMINATION OF LIVER LEFT/RIGHT ASYMMETRY | 14 | -0.45 | -1.12 | 0.342 | 0.775 | 1.000 | 12002 | tags=50%, list=22%, signal=64% | |
1758 | RELAXATION OF MUSCLE | 35 | -0.32 | -1.12 | 0.287 | 0.774 | 1.000 | 17609 | tags=40%, list=32%, signal=59% | |
1759 | RESPONSE TO HEXOSE | 101 | -0.29 | -1.12 | 0.328 | 0.774 | 1.000 | 17426 | tags=43%, list=32%, signal=62% | |
1760 | RESPONSE TO MONOSACCHARIDE | 101 | -0.29 | -1.12 | 0.328 | 0.774 | 1.000 | 17426 | tags=43%, list=32%, signal=62% | |
1761 | NADP METABOLIC PROCESS | 41 | -0.34 | -1.12 | 0.328 | 0.774 | 1.000 | 22945 | tags=59%, list=42%, signal=101% | |
1762 | PEPTIDYL-SERINE MODIFICATION | 273 | -0.29 | -1.12 | 0.342 | 0.775 | 1.000 | 24622 | tags=56%, list=45%, signal=101% | |
1763 | POSITIVE REGULATION OF PROTEIN SERINE/THREONINE KINASE ACTIVITY | 491 | -0.27 | -1.12 | 0.298 | 0.774 | 1.000 | 20173 | tags=43%, list=37%, signal=67% | |
1764 | NOTCH SIGNALING INVOLVED IN HEART DEVELOPMENT | 10 | -0.44 | -1.12 | 0.345 | 0.775 | 1.000 | 12962 | tags=40%, list=24%, signal=52% | |
1765 | PROTEIN LOCALIZATION TO CELL SURFACE | 45 | -0.32 | -1.12 | 0.319 | 0.776 | 1.000 | 23703 | tags=56%, list=43%, signal=98% | |
1766 | POSITIVE REGULATION OF NATURAL KILLER CELL MEDIATED IMMUNITY | 40 | -0.34 | -1.12 | 0.342 | 0.776 | 1.000 | 16819 | tags=45%, list=31%, signal=65% | |
1767 | LYSOSOMAL TRANSPORT | 133 | -0.31 | -1.12 | 0.297 | 0.776 | 1.000 | 25826 | tags=61%, list=47%, signal=115% | |
1768 | REGULATION OF CYTOPLASMIC MRNA PROCESSING BODY ASSEMBLY | 16 | -0.40 | -1.12 | 0.341 | 0.776 | 1.000 | 22164 | tags=63%, list=41%, signal=105% | |
1769 | DNA STRAND ELONGATION INVOLVED IN DNA REPLICATION | 63 | -0.32 | -1.12 | 0.331 | 0.776 | 1.000 | 27390 | tags=70%, list=50%, signal=140% | |
1770 | PENTOSE METABOLIC PROCESS | 10 | -0.45 | -1.11 | 0.305 | 0.775 | 1.000 | 11527 | tags=50%, list=21%, signal=63% | |
1771 | REGULATION OF CHROMOSOME SEGREGATION | 203 | -0.32 | -1.11 | 0.362 | 0.776 | 1.000 | 24486 | tags=61%, list=45%, signal=109% | |
1772 | ENTRAINMENT OF CIRCADIAN CLOCK | 60 | -0.31 | -1.11 | 0.333 | 0.776 | 1.000 | 23193 | tags=57%, list=42%, signal=98% | |
1773 | GLUTAMINE FAMILY AMINO ACID METABOLIC PROCESS | 76 | -0.32 | -1.11 | 0.323 | 0.776 | 1.000 | 25606 | tags=63%, list=47%, signal=119% | |
1774 | POLYSACCHARIDE METABOLIC PROCESS | 107 | -0.30 | -1.11 | 0.324 | 0.776 | 1.000 | 20229 | tags=48%, list=37%, signal=76% | |
1775 | REGULATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC PROCESS | 442 | -0.29 | -1.11 | 0.336 | 0.775 | 1.000 | 21279 | tags=51%, list=39%, signal=82% | |
1776 | REGULATION OF RESPONSE TO TUMOR CELL | 27 | -0.34 | -1.11 | 0.344 | 0.776 | 1.000 | 17597 | tags=48%, list=32%, signal=71% | |
1777 | REGULATION OF IMMUNE RESPONSE TO TUMOR CELL | 27 | -0.34 | -1.11 | 0.344 | 0.776 | 1.000 | 17597 | tags=48%, list=32%, signal=71% | |
1778 | MATURE B CELL DIFFERENTIATION INVOLVED IN IMMUNE RESPONSE | 15 | -0.36 | -1.11 | 0.302 | 0.777 | 1.000 | 11535 | tags=33%, list=21%, signal=42% | |
1779 | MATURE B CELL DIFFERENTIATION | 15 | -0.36 | -1.11 | 0.302 | 0.776 | 1.000 | 11535 | tags=33%, list=21%, signal=42% | |
1780 | REGULATION OF CHROMATIN MODIFICATION | 257 | -0.29 | -1.11 | 0.276 | 0.776 | 1.000 | 15813 | tags=40%, list=29%, signal=56% | |
1781 | HISTONE METHYLATION | 163 | -0.31 | -1.11 | 0.367 | 0.776 | 1.000 | 27726 | tags=65%, list=51%, signal=132% | |
1782 | HISTONE MRNA METABOLIC PROCESS | 57 | -0.36 | -1.11 | 0.395 | 0.776 | 1.000 | 29395 | tags=77%, list=54%, signal=167% | |
1783 | NCRNA 3'-END PROCESSING | 12 | -0.44 | -1.11 | 0.339 | 0.776 | 1.000 | 18960 | tags=67%, list=35%, signal=102% | |
1784 | PYRIDINE-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 16 | -0.42 | -1.11 | 0.369 | 0.777 | 1.000 | 16762 | tags=56%, list=31%, signal=81% | |
1785 | NEGATIVE REGULATION OF CENTRIOLE REPLICATION | 12 | -0.44 | -1.11 | 0.366 | 0.776 | 1.000 | 25404 | tags=75%, list=46%, signal=140% | |
1786 | RESPONSE TO ACIDIC PH | 19 | -0.38 | -1.11 | 0.328 | 0.776 | 1.000 | 31044 | tags=84%, list=57%, signal=195% | |
1787 | LIPID PHOSPHORYLATION | 80 | -0.32 | -1.11 | 0.303 | 0.776 | 1.000 | 14342 | tags=39%, list=26%, signal=52% | |
1788 | TRIF-DEPENDENT TOLL-LIKE RECEPTOR SIGNALING PATHWAY | 203 | -0.31 | -1.11 | 0.358 | 0.776 | 1.000 | 18444 | tags=47%, list=34%, signal=71% | |
1789 | REGULATION OF PERK-MEDIATED UNFOLDED PROTEIN RESPONSE | 14 | -0.40 | -1.11 | 0.317 | 0.776 | 1.000 | 20480 | tags=64%, list=37%, signal=103% | |
1790 | REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 223 | -0.29 | -1.11 | 0.323 | 0.776 | 1.000 | 17975 | tags=42%, list=33%, signal=63% | |
1791 | REGULATION OF TRANSCRIPTION INVOLVED IN G1/S TRANSITION OF MITOTIC CELL CYCLE | 51 | -0.34 | -1.11 | 0.352 | 0.776 | 1.000 | 20376 | tags=49%, list=37%, signal=78% | |
1792 | CIRCADIAN RHYTHM | 266 | -0.29 | -1.11 | 0.303 | 0.776 | 1.000 | 22427 | tags=52%, list=41%, signal=88% | |
1793 | NEGATIVE REGULATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC PROCESS | 210 | -0.29 | -1.11 | 0.360 | 0.776 | 1.000 | 20653 | tags=50%, list=38%, signal=80% | |
1794 | EPITHELIAL CILIUM MOVEMENT | 15 | -0.45 | -1.11 | 0.358 | 0.776 | 1.000 | 17345 | tags=60%, list=32%, signal=88% | |
1795 | POSITIVE REGULATION OF INTRACELLULAR TRANSPORT | 698 | -0.28 | -1.11 | 0.253 | 0.776 | 1.000 | 26192 | tags=57%, list=48%, signal=108% | |
1796 | REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 699 | -0.28 | -1.11 | 0.242 | 0.775 | 1.000 | 25937 | tags=56%, list=47%, signal=105% | |
1797 | SMOOTHENED SIGNALING PATHWAY | 69 | -0.31 | -1.11 | 0.342 | 0.777 | 1.000 | 19517 | tags=49%, list=36%, signal=77% | |
1798 | ENDOCYTIC RECYCLING | 58 | -0.33 | -1.11 | 0.333 | 0.776 | 1.000 | 17960 | tags=48%, list=33%, signal=72% | |
1799 | MYELOID CELL DIFFERENTIATION | 231 | -0.28 | -1.11 | 0.377 | 0.776 | 1.000 | 23245 | tags=50%, list=43%, signal=87% | |
1800 | ASYMMETRIC CELL DIVISION | 23 | -0.38 | -1.11 | 0.355 | 0.777 | 1.000 | 12051 | tags=39%, list=22%, signal=50% | |
1801 | GLIAL CELL DEVELOPMENT | 77 | -0.31 | -1.11 | 0.336 | 0.776 | 1.000 | 28781 | tags=70%, list=53%, signal=148% | |
1802 | ALPHA-AMINO ACID BIOSYNTHETIC PROCESS | 97 | -0.30 | -1.11 | 0.325 | 0.776 | 1.000 | 27453 | tags=63%, list=50%, signal=126% | |
1803 | POSITIVE REGULATION OF CHROMOSOME ORGANIZATION | 309 | -0.30 | -1.11 | 0.269 | 0.776 | 1.000 | 18679 | tags=45%, list=34%, signal=67% | |
1804 | REGULATION OF STEROL TRANSPORT | 56 | -0.32 | -1.11 | 0.344 | 0.776 | 1.000 | 19886 | tags=45%, list=36%, signal=70% | |
1805 | REGULATION OF CHOLESTEROL TRANSPORT | 56 | -0.32 | -1.11 | 0.344 | 0.776 | 1.000 | 19886 | tags=45%, list=36%, signal=70% | |
1806 | NEGATIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE/THREONINE KINASE SIGNALING PATHWAY | 190 | -0.29 | -1.11 | 0.287 | 0.776 | 1.000 | 20480 | tags=47%, list=37%, signal=75% | |
1807 | REGULATION OF CHROMATIN ORGANIZATION | 283 | -0.28 | -1.11 | 0.282 | 0.775 | 1.000 | 16930 | tags=41%, list=31%, signal=59% | |
1808 | POSITIVE REGULATION OF INTRACELLULAR ESTROGEN RECEPTOR SIGNALING PATHWAY | 18 | -0.41 | -1.11 | 0.353 | 0.776 | 1.000 | 22488 | tags=56%, list=41%, signal=94% | |
1809 | NEGATIVE REGULATION OF CELL SIZE | 18 | -0.40 | -1.11 | 0.364 | 0.776 | 1.000 | 18246 | tags=56%, list=33%, signal=83% | |
1810 | ANTIGEN RECEPTOR-MEDIATED SIGNALING PATHWAY | 372 | -0.30 | -1.11 | 0.355 | 0.776 | 1.000 | 23257 | tags=54%, list=43%, signal=93% | |
1811 | ALCOHOL METABOLIC PROCESS | 505 | -0.27 | -1.11 | 0.250 | 0.776 | 1.000 | 23100 | tags=51%, list=42%, signal=87% | |
1812 | NEGATIVE REGULATION OF POSTTRANSCRIPTIONAL GENE SILENCING | 9 | -0.44 | -1.11 | 0.344 | 0.777 | 1.000 | 6172 | tags=33%, list=11%, signal=38% | |
1813 | NEGATIVE REGULATION OF GENE SILENCING BY RNA | 9 | -0.44 | -1.11 | 0.344 | 0.776 | 1.000 | 6172 | tags=33%, list=11%, signal=38% | |
1814 | NEGATIVE REGULATION OF VOLTAGE-GATED POTASSIUM CHANNEL ACTIVITY | 24 | -0.34 | -1.11 | 0.328 | 0.776 | 1.000 | 25853 | tags=58%, list=47%, signal=111% | |
1815 | REGULATION OF ACTIN CYTOSKELETON REORGANIZATION | 49 | -0.31 | -1.11 | 0.356 | 0.776 | 1.000 | 20529 | tags=41%, list=38%, signal=65% | |
1816 | NEGATIVE REGULATION OF TRANSLATION | 270 | -0.30 | -1.11 | 0.330 | 0.776 | 1.000 | 22585 | tags=55%, list=41%, signal=93% | |
1817 | DESENSITIZATION OF G-PROTEIN COUPLED RECEPTOR PROTEIN SIGNALING PATHWAY | 21 | -0.36 | -1.11 | 0.329 | 0.776 | 1.000 | 22297 | tags=52%, list=41%, signal=88% | |
1818 | NEGATIVE ADAPTATION OF SIGNALING PATHWAY | 21 | -0.36 | -1.11 | 0.329 | 0.775 | 1.000 | 22297 | tags=52%, list=41%, signal=88% | |
1819 | ADAPTATION OF SIGNALING PATHWAY | 21 | -0.36 | -1.11 | 0.329 | 0.775 | 1.000 | 22297 | tags=52%, list=41%, signal=88% | |
1820 | PROTEIN KINASE C SIGNALING | 24 | -0.37 | -1.11 | 0.338 | 0.775 | 1.000 | 11496 | tags=33%, list=21%, signal=42% | |
1821 | RESPONSE TO RETINOIC ACID | 125 | -0.28 | -1.11 | 0.337 | 0.775 | 1.000 | 15194 | tags=37%, list=28%, signal=51% | |
1822 | GROWTH HORMONE RECEPTOR SIGNALING PATHWAY | 89 | -0.30 | -1.11 | 0.341 | 0.776 | 1.000 | 25689 | tags=56%, list=47%, signal=106% | |
1823 | CELLULAR RESPONSE TO GROWTH HORMONE STIMULUS | 89 | -0.30 | -1.11 | 0.341 | 0.775 | 1.000 | 25689 | tags=56%, list=47%, signal=106% | |
1824 | NEUTROPHIL MEDIATED IMMUNITY | 18 | -0.42 | -1.11 | 0.396 | 0.775 | 1.000 | 25019 | tags=78%, list=46%, signal=143% | |
1825 | NEGATIVE REGULATION OF POTASSIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 35 | -0.31 | -1.11 | 0.328 | 0.775 | 1.000 | 25853 | tags=57%, list=47%, signal=108% | |
1826 | REGULATION OF MACROPHAGE APOPTOTIC PROCESS | 10 | -0.43 | -1.11 | 0.320 | 0.775 | 1.000 | 27588 | tags=80%, list=50%, signal=161% | |
1827 | NEUROTROPHIN SIGNALING PATHWAY | 1116 | -0.25 | -1.11 | 0.254 | 0.775 | 1.000 | 26927 | tags=55%, list=49%, signal=106% | |
1828 | ESTABLISHMENT OR MAINTENANCE OF APICAL/BASAL CELL POLARITY | 20 | -0.36 | -1.11 | 0.306 | 0.775 | 1.000 | 8040 | tags=25%, list=15%, signal=29% | |
1829 | ESTABLISHMENT OR MAINTENANCE OF BIPOLAR CELL POLARITY | 20 | -0.36 | -1.11 | 0.306 | 0.774 | 1.000 | 8040 | tags=25%, list=15%, signal=29% | |
1830 | NEGATIVE REGULATION OF CARDIAC MUSCLE HYPERTROPHY | 12 | -0.40 | -1.11 | 0.331 | 0.774 | 1.000 | 13266 | tags=42%, list=24%, signal=55% | |
1831 | NEGATIVE REGULATION OF MUSCLE HYPERTROPHY | 12 | -0.40 | -1.11 | 0.331 | 0.773 | 1.000 | 13266 | tags=42%, list=24%, signal=55% | |
1832 | POSITIVE REGULATION OF CHROMOSOME SEGREGATION | 40 | -0.37 | -1.11 | 0.368 | 0.773 | 1.000 | 21691 | tags=63%, list=40%, signal=104% | |
1833 | FAT CELL DIFFERENTIATION | 127 | -0.29 | -1.11 | 0.359 | 0.773 | 1.000 | 25822 | tags=57%, list=47%, signal=109% | |
1834 | TYPE I INTERFERON SIGNALING PATHWAY | 137 | -0.32 | -1.11 | 0.377 | 0.773 | 1.000 | 22839 | tags=56%, list=42%, signal=96% | |
1835 | CELLULAR RESPONSE TO TYPE I INTERFERON | 137 | -0.32 | -1.11 | 0.377 | 0.773 | 1.000 | 22839 | tags=56%, list=42%, signal=96% | |
1836 | REGULATION OF ACTIN POLYMERIZATION OR DEPOLYMERIZATION | 190 | -0.29 | -1.11 | 0.301 | 0.773 | 1.000 | 19703 | tags=46%, list=36%, signal=71% | |
1837 | REGULATION OF ACTIN FILAMENT LENGTH | 190 | -0.29 | -1.11 | 0.301 | 0.773 | 1.000 | 19703 | tags=46%, list=36%, signal=71% | |
1838 | PEROXISOME ORGANIZATION | 75 | -0.35 | -1.11 | 0.387 | 0.772 | 1.000 | 17894 | tags=53%, list=33%, signal=79% | |
1839 | COFACTOR CATABOLIC PROCESS | 30 | -0.37 | -1.11 | 0.360 | 0.772 | 1.000 | 32422 | tags=90%, list=59%, signal=221% | |
1840 | REGULATION OF CELL CYCLE CHECKPOINT | 46 | -0.35 | -1.11 | 0.375 | 0.772 | 1.000 | 26137 | tags=67%, list=48%, signal=129% | |
1841 | NUCLEAR CHROMOSOME SEGREGATION | 229 | -0.30 | -1.11 | 0.318 | 0.772 | 1.000 | 21773 | tags=52%, list=40%, signal=85% | |
1842 | MITOCHONDRIAL FUSION | 30 | -0.39 | -1.11 | 0.397 | 0.772 | 1.000 | 11572 | tags=43%, list=21%, signal=55% | |
1843 | ACTIVATION OF MAPKKK ACTIVITY | 16 | -0.40 | -1.11 | 0.330 | 0.772 | 1.000 | 23508 | tags=56%, list=43%, signal=99% | |
1844 | PROTEIN DEMETHYLATION | 52 | -0.33 | -1.11 | 0.356 | 0.771 | 1.000 | 22418 | tags=56%, list=41%, signal=94% | |
1845 | PROTEIN DEALKYLATION | 52 | -0.33 | -1.11 | 0.356 | 0.771 | 1.000 | 22418 | tags=56%, list=41%, signal=94% | |
1846 | G2/M TRANSITION OF MITOTIC CELL CYCLE | 330 | -0.30 | -1.11 | 0.303 | 0.771 | 1.000 | 18752 | tags=47%, list=34%, signal=71% | |
1847 | CELL CYCLE G2/M PHASE TRANSITION | 330 | -0.30 | -1.11 | 0.303 | 0.771 | 1.000 | 18752 | tags=47%, list=34%, signal=71% | |
1848 | HEMATOPOIETIC STEM CELL PROLIFERATION | 36 | -0.33 | -1.11 | 0.333 | 0.770 | 1.000 | 28397 | tags=67%, list=52%, signal=139% | |
1849 | POSITIVE REGULATION OF LEUKOCYTE MEDIATED CYTOTOXICITY | 61 | -0.33 | -1.11 | 0.363 | 0.770 | 1.000 | 17332 | tags=44%, list=32%, signal=65% | |
1850 | POSITIVE REGULATION OF PROTEIN TRANSPORT | 739 | -0.27 | -1.11 | 0.282 | 0.770 | 1.000 | 22892 | tags=49%, list=42%, signal=84% | |
1851 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 880 | -0.27 | -1.11 | 0.285 | 0.770 | 1.000 | 25892 | tags=56%, list=47%, signal=104% | |
1852 | PHAGOSOME MATURATION | 20 | -0.41 | -1.10 | 0.378 | 0.770 | 1.000 | 19071 | tags=60%, list=35%, signal=92% | |
1853 | ACTIVATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC PROCESS | 197 | -0.32 | -1.10 | 0.361 | 0.770 | 1.000 | 21279 | tags=54%, list=39%, signal=89% | |
1854 | MORPHOGENESIS OF A POLARIZED EPITHELIUM | 17 | -0.41 | -1.10 | 0.393 | 0.770 | 1.000 | 22701 | tags=71%, list=42%, signal=121% | |
1855 | POSITIVE REGULATION OF DNA METABOLIC PROCESS | 322 | -0.28 | -1.10 | 0.270 | 0.772 | 1.000 | 22721 | tags=49%, list=42%, signal=84% | |
1856 | RESPONSE TO SALT STRESS | 12 | -0.47 | -1.10 | 0.376 | 0.772 | 1.000 | 15296 | tags=58%, list=28%, signal=81% | |
1857 | NUCLEAR EXPORT | 251 | -0.32 | -1.10 | 0.373 | 0.771 | 1.000 | 22937 | tags=57%, list=42%, signal=98% | |
1858 | HISTONE LYSINE METHYLATION | 135 | -0.31 | -1.10 | 0.376 | 0.771 | 1.000 | 27726 | tags=64%, list=51%, signal=129% | |
1859 | VALINE METABOLIC PROCESS | 15 | -0.42 | -1.10 | 0.356 | 0.771 | 1.000 | 27510 | tags=87%, list=50%, signal=174% | |
1860 | PROTEIN TO MEMBRANE DOCKING | 20 | -0.41 | -1.10 | 0.394 | 0.771 | 1.000 | 25770 | tags=80%, list=47%, signal=151% | |
1861 | RELAXATION OF CARDIAC MUSCLE | 32 | -0.33 | -1.10 | 0.309 | 0.771 | 1.000 | 17609 | tags=41%, list=32%, signal=60% | |
1862 | NEGATIVE REGULATION OF STRIATED MUSCLE CELL DIFFERENTIATION | 41 | -0.34 | -1.10 | 0.358 | 0.771 | 1.000 | 16694 | tags=44%, list=31%, signal=63% | |
1863 | DICARBOXYLIC ACID BIOSYNTHETIC PROCESS | 18 | -0.41 | -1.10 | 0.388 | 0.771 | 1.000 | 26219 | tags=78%, list=48%, signal=149% | |
1864 | ADENYLATE CYCLASE-ACTIVATING G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 81 | -0.29 | -1.10 | 0.326 | 0.772 | 1.000 | 12581 | tags=28%, list=23%, signal=37% | |
1865 | CELLULAR RESPONSE TO EXTERNAL STIMULUS | 318 | -0.30 | -1.10 | 0.353 | 0.772 | 1.000 | 22217 | tags=53%, list=41%, signal=90% | |
1866 | POSITIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 289 | -0.27 | -1.10 | 0.317 | 0.773 | 1.000 | 17655 | tags=40%, list=32%, signal=58% | |
1867 | SENSORY PERCEPTION OF SWEET TASTE | 2 | -0.70 | -1.10 | 0.359 | 0.773 | 1.000 | 336 | tags=50%, list=1%, signal=50% | |
1868 | NEGATIVE REGULATION OF TRANSCRIPTION BY COMPETITIVE PROMOTER BINDING | 28 | -0.38 | -1.10 | 0.379 | 0.773 | 1.000 | 24611 | tags=71%, list=45%, signal=130% | |
1869 | MICROTUBULE-BASED PROCESS | 764 | -0.30 | -1.10 | 0.326 | 0.773 | 1.000 | 27400 | tags=64%, list=50%, signal=126% | |
1870 | PROTEIN TARGETING TO PEROXISOME | 42 | -0.37 | -1.10 | 0.353 | 0.774 | 1.000 | 32745 | tags=93%, list=60%, signal=231% | |
1871 | PEROXISOMAL TRANSPORT | 42 | -0.37 | -1.10 | 0.353 | 0.774 | 1.000 | 32745 | tags=93%, list=60%, signal=231% | |
1872 | PROTEIN LOCALIZATION TO PEROXISOME | 42 | -0.37 | -1.10 | 0.353 | 0.773 | 1.000 | 32745 | tags=93%, list=60%, signal=231% | |
1873 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO PEROXISOME | 42 | -0.37 | -1.10 | 0.353 | 0.773 | 1.000 | 32745 | tags=93%, list=60%, signal=231% | |
1874 | POSITIVE REGULATION OF MITOCHONDRIAL CALCIUM ION CONCENTRATION | 16 | -0.40 | -1.10 | 0.361 | 0.773 | 1.000 | 16836 | tags=56%, list=31%, signal=81% | |
1875 | PEPTIDYL-LYSINE METHYLATION | 144 | -0.31 | -1.10 | 0.370 | 0.773 | 1.000 | 27726 | tags=64%, list=51%, signal=129% | |
1876 | OXALOACETATE METABOLIC PROCESS | 11 | -0.47 | -1.10 | 0.413 | 0.772 | 1.000 | 22720 | tags=82%, list=42%, signal=140% | |
1877 | TYPE B PANCREATIC CELL PROLIFERATION | 7 | -0.48 | -1.10 | 0.383 | 0.773 | 1.000 | 17971 | tags=57%, list=33%, signal=85% | |
1878 | REGULATION OF LEUKOCYTE DEGRANULATION | 46 | -0.33 | -1.10 | 0.379 | 0.774 | 1.000 | 12087 | tags=35%, list=22%, signal=45% | |
1879 | NEURAL NUCLEUS DEVELOPMENT | 132 | -0.31 | -1.10 | 0.326 | 0.775 | 1.000 | 23136 | tags=57%, list=42%, signal=98% | |
1880 | NODAL SIGNALING PATHWAY | 24 | -0.35 | -1.10 | 0.339 | 0.775 | 1.000 | 18797 | tags=50%, list=34%, signal=76% | |
1881 | NUCLEAR DIVISION | 416 | -0.29 | -1.10 | 0.252 | 0.775 | 1.000 | 21849 | tags=50%, list=40%, signal=83% | |
1882 | NEGATIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 1079 | -0.28 | -1.10 | 0.229 | 0.775 | 1.000 | 19558 | tags=45%, list=36%, signal=69% | |
1883 | TERMINATION OF RNA POLYMERASE II TRANSCRIPTION | 117 | -0.34 | -1.10 | 0.410 | 0.775 | 1.000 | 23769 | tags=62%, list=43%, signal=110% | |
1884 | POSITIVE REGULATION OF DNA REPLICATION | 171 | -0.28 | -1.10 | 0.328 | 0.775 | 1.000 | 23271 | tags=51%, list=43%, signal=88% | |
1885 | NEURON DEATH | 59 | -0.31 | -1.10 | 0.358 | 0.775 | 1.000 | 25567 | tags=59%, list=47%, signal=111% | |
1886 | SULFUR AMINO ACID BIOSYNTHETIC PROCESS | 38 | -0.34 | -1.10 | 0.375 | 0.775 | 1.000 | 27293 | tags=71%, list=50%, signal=142% | |
1887 | POSITIVE REGULATION OF SEQUENCE-SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 485 | -0.27 | -1.10 | 0.395 | 0.775 | 1.000 | 23814 | tags=52%, list=44%, signal=91% | |
1888 | RESPONSE TO OXIDATIVE STRESS | 390 | -0.28 | -1.10 | 0.296 | 0.775 | 1.000 | 23814 | tags=53%, list=44%, signal=92% | |
1889 | REGULATION OF TRIGLYCERIDE BIOSYNTHETIC PROCESS | 37 | -0.31 | -1.10 | 0.334 | 0.774 | 1.000 | 16447 | tags=41%, list=30%, signal=58% | |
1890 | REGULATION OF INCLUSION BODY ASSEMBLY | 32 | -0.38 | -1.10 | 0.378 | 0.774 | 1.000 | 33167 | tags=97%, list=61%, signal=246% | |
1891 | PEPTIDYL-SERINE PHOSPHORYLATION | 259 | -0.28 | -1.10 | 0.359 | 0.774 | 1.000 | 22667 | tags=51%, list=41%, signal=87% | |
1892 | LIPID PARTICLE ORGANIZATION | 34 | -0.35 | -1.10 | 0.354 | 0.774 | 1.000 | 29616 | tags=76%, list=54%, signal=167% | |
1893 | COBALAMIN METABOLIC PROCESS | 36 | -0.33 | -1.10 | 0.330 | 0.774 | 1.000 | 18055 | tags=47%, list=33%, signal=70% | |
1894 | POSITIVE REGULATION OF REGULATED SECRETORY PATHWAY | 52 | -0.30 | -1.10 | 0.327 | 0.774 | 1.000 | 16852 | tags=40%, list=31%, signal=58% | |
1895 | DENDRITE MORPHOGENESIS | 60 | -0.28 | -1.10 | 0.351 | 0.774 | 1.000 | 22697 | tags=52%, list=42%, signal=88% | |
1896 | NEGATIVE REGULATION OF PROTEOLYSIS | 586 | -0.28 | -1.10 | 0.318 | 0.774 | 1.000 | 19406 | tags=44%, list=35%, signal=68% | |
1897 | ACTIVATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY | 219 | -0.31 | -1.10 | 0.396 | 0.773 | 1.000 | 22215 | tags=55%, list=41%, signal=93% | |
1898 | REGULATION OF SYNAPTIC VESICLE EXOCYTOSIS | 20 | -0.37 | -1.10 | 0.357 | 0.773 | 1.000 | 15593 | tags=45%, list=29%, signal=63% | |
1899 | NEUTRAL LIPID BIOSYNTHETIC PROCESS | 132 | -0.30 | -1.10 | 0.361 | 0.774 | 1.000 | 24351 | tags=56%, list=45%, signal=101% | |
1900 | ACYLGLYCEROL BIOSYNTHETIC PROCESS | 132 | -0.30 | -1.10 | 0.361 | 0.774 | 1.000 | 24351 | tags=56%, list=45%, signal=101% | |
1901 | POSITIVE REGULATION OF CYTOKINE-MEDIATED SIGNALING PATHWAY | 35 | -0.32 | -1.10 | 0.324 | 0.774 | 1.000 | 24118 | tags=57%, list=44%, signal=102% | |
1902 | REGULATION OF DNA REPAIR | 160 | -0.29 | -1.10 | 0.353 | 0.775 | 1.000 | 23257 | tags=52%, list=43%, signal=91% | |
1903 | REGULATION OF NECROPTOTIC PROCESS | 29 | -0.39 | -1.10 | 0.388 | 0.774 | 1.000 | 23528 | tags=69%, list=43%, signal=121% | |
1904 | POSITIVE REGULATION OF MYELINATION | 16 | -0.38 | -1.10 | 0.370 | 0.775 | 1.000 | 21709 | tags=56%, list=40%, signal=93% | |
1905 | NEGATIVE REGULATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY | 215 | -0.29 | -1.10 | 0.378 | 0.775 | 1.000 | 20653 | tags=50%, list=38%, signal=80% | |
1906 | REGULATION OF RECEPTOR-MEDIATED ENDOCYTOSIS | 188 | -0.27 | -1.10 | 0.361 | 0.776 | 1.000 | 16716 | tags=38%, list=31%, signal=54% | |
1907 | DNA REPLICATION | 335 | -0.29 | -1.10 | 0.294 | 0.776 | 1.000 | 20547 | tags=47%, list=38%, signal=75% | |
1908 | ATRIOVENTRICULAR VALVE MORPHOGENESIS | 25 | -0.35 | -1.10 | 0.352 | 0.776 | 1.000 | 25051 | tags=60%, list=46%, signal=111% | |
1909 | PRE-MIRNA PROCESSING | 24 | -0.37 | -1.10 | 0.362 | 0.775 | 1.000 | 29795 | tags=79%, list=54%, signal=174% | |
1910 | NUCLEOTIDE TRANSMEMBRANE TRANSPORT | 29 | -0.36 | -1.10 | 0.372 | 0.775 | 1.000 | 9403 | tags=34%, list=17%, signal=42% | |
1911 | DNA TOPOLOGICAL CHANGE | 17 | -0.39 | -1.10 | 0.362 | 0.775 | 1.000 | 16702 | tags=47%, list=31%, signal=68% | |
1912 | REGULATION OF JUN KINASE ACTIVITY | 118 | -0.30 | -1.09 | 0.350 | 0.774 | 1.000 | 20084 | tags=48%, list=37%, signal=76% | |
1913 | NEGATIVE REGULATION OF MULTI-ORGANISM PROCESS | 275 | -0.28 | -1.09 | 0.335 | 0.775 | 1.000 | 19204 | tags=44%, list=35%, signal=67% | |
1914 | HAIR CELL DIFFERENTIATION | 16 | -0.40 | -1.09 | 0.369 | 0.775 | 1.000 | 23703 | tags=69%, list=43%, signal=121% | |
1915 | NEGATIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 181 | -0.28 | -1.09 | 0.336 | 0.774 | 1.000 | 23310 | tags=50%, list=43%, signal=87% | |
1916 | REGULATION OF AMYLOID PRECURSOR PROTEIN CATABOLIC PROCESS | 30 | -0.36 | -1.09 | 0.373 | 0.775 | 1.000 | 25281 | tags=67%, list=46%, signal=124% | |
1917 | REGULATION OF MIRNA METABOLIC PROCESS | 6 | -0.50 | -1.09 | 0.371 | 0.774 | 1.000 | 27337 | tags=100%, list=50%, signal=200% | |
1918 | POSITIVE REGULATION OF MIRNA METABOLIC PROCESS | 6 | -0.50 | -1.09 | 0.371 | 0.774 | 1.000 | 27337 | tags=100%, list=50%, signal=200% | |
1919 | ORGANELLE TRANSPORT ALONG MICROTUBULE | 106 | -0.32 | -1.09 | 0.341 | 0.774 | 1.000 | 19923 | tags=53%, list=36%, signal=83% | |
1920 | POSITIVE REGULATION OF LIPOPROTEIN LIPASE ACTIVITY | 12 | -0.45 | -1.09 | 0.360 | 0.774 | 1.000 | 4646 | tags=25%, list=8%, signal=27% | |
1921 | ORGANELLE FISSION | 472 | -0.29 | -1.09 | 0.298 | 0.774 | 1.000 | 21893 | tags=50%, list=40%, signal=83% | |
1922 | TAURINE METABOLIC PROCESS | 10 | -0.48 | -1.09 | 0.385 | 0.774 | 1.000 | 22720 | tags=80%, list=42%, signal=137% | |
1923 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 207 | -0.29 | -1.09 | 0.343 | 0.774 | 1.000 | 29089 | tags=64%, list=53%, signal=136% | |
1924 | SOMATIC DIVERSIFICATION OF IMMUNE RECEPTORS VIA GERMLINE RECOMBINATION WITHIN A SINGLE LOCUS | 54 | -0.31 | -1.09 | 0.338 | 0.774 | 1.000 | 18286 | tags=44%, list=33%, signal=67% | |
1925 | SOMATIC CELL DNA RECOMBINATION | 54 | -0.31 | -1.09 | 0.338 | 0.773 | 1.000 | 18286 | tags=44%, list=33%, signal=67% | |
1926 | RESPONSE TO RADIATION | 729 | -0.26 | -1.09 | 0.231 | 0.773 | 1.000 | 19314 | tags=43%, list=35%, signal=66% | |
1927 | REGULATION OF NEUTROPHIL MIGRATION | 39 | -0.34 | -1.09 | 0.382 | 0.773 | 1.000 | 19058 | tags=46%, list=35%, signal=71% | |
1928 | FEMALE GAMETE GENERATION | 62 | -0.30 | -1.09 | 0.351 | 0.773 | 1.000 | 9020 | tags=26%, list=16%, signal=31% | |
1929 | NON-RECOMBINATIONAL REPAIR | 142 | -0.30 | -1.09 | 0.371 | 0.772 | 1.000 | 29086 | tags=67%, list=53%, signal=143% | |
1930 | ENERGY RESERVE METABOLIC PROCESS | 317 | -0.26 | -1.09 | 0.309 | 0.772 | 1.000 | 22601 | tags=47%, list=41%, signal=79% | |
1931 | CYTOSKELETON-DEPENDENT INTRACELLULAR TRANSPORT | 194 | -0.31 | -1.09 | 0.342 | 0.773 | 1.000 | 25643 | tags=61%, list=47%, signal=115% | |
1932 | INTERFERON-GAMMA PRODUCTION | 14 | -0.42 | -1.09 | 0.373 | 0.773 | 1.000 | 28163 | tags=86%, list=52%, signal=177% | |
1933 | HISTONE H3-K9 MODIFICATION | 22 | -0.37 | -1.09 | 0.381 | 0.772 | 1.000 | 27726 | tags=73%, list=51%, signal=147% | |
1934 | AMINO SUGAR CATABOLIC PROCESS | 11 | -0.41 | -1.09 | 0.366 | 0.772 | 1.000 | 8109 | tags=36%, list=15%, signal=43% | |
1935 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 220 | -0.27 | -1.09 | 0.337 | 0.772 | 1.000 | 20480 | tags=47%, list=37%, signal=75% | |
1936 | REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 220 | -0.27 | -1.09 | 0.337 | 0.772 | 1.000 | 20480 | tags=47%, list=37%, signal=75% | |
1937 | POSITIVE REGULATION OF TELOMERE MAINTENANCE | 124 | -0.31 | -1.09 | 0.348 | 0.772 | 1.000 | 18614 | tags=47%, list=34%, signal=71% | |
1938 | REGULATION OF MITOCHONDRIAL FISSION | 35 | -0.35 | -1.09 | 0.391 | 0.772 | 1.000 | 29852 | tags=77%, list=55%, signal=170% | |
1939 | CELLULAR RESPONSE TO PEPTIDE | 1019 | -0.25 | -1.09 | 0.331 | 0.773 | 1.000 | 25186 | tags=51%, list=46%, signal=92% | |
1940 | PROTEIN DEACETYLATION | 86 | -0.29 | -1.09 | 0.363 | 0.773 | 1.000 | 28257 | tags=63%, list=52%, signal=130% | |
1941 | PROTEIN DEACYLATION | 88 | -0.28 | -1.09 | 0.360 | 0.773 | 1.000 | 28257 | tags=63%, list=52%, signal=129% | |
1942 | CELLULAR RESPONSE TO PEPTIDE HORMONE STIMULUS | 1004 | -0.25 | -1.09 | 0.326 | 0.773 | 1.000 | 26842 | tags=54%, list=49%, signal=104% | |
1943 | BRANCHED-CHAIN AMINO ACID METABOLIC PROCESS | 65 | -0.32 | -1.09 | 0.354 | 0.773 | 1.000 | 27903 | tags=68%, list=51%, signal=138% | |
1944 | IMMUNE RESPONSE-ACTIVATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 734 | -0.28 | -1.09 | 0.351 | 0.773 | 1.000 | 23257 | tags=50%, list=43%, signal=86% | |
1945 | MYELINATION | 95 | -0.29 | -1.09 | 0.363 | 0.774 | 1.000 | 25958 | tags=60%, list=47%, signal=114% | |
1946 | PROLINE METABOLIC PROCESS | 10 | -0.47 | -1.09 | 0.388 | 0.774 | 1.000 | 28754 | tags=90%, list=53%, signal=190% | |
1947 | INSULIN RECEPTOR SIGNALING PATHWAY | 766 | -0.26 | -1.09 | 0.267 | 0.774 | 1.000 | 26842 | tags=56%, list=49%, signal=108% | |
1948 | HISTONE H3-K9 METHYLATION | 19 | -0.37 | -1.09 | 0.386 | 0.774 | 1.000 | 23849 | tags=63%, list=44%, signal=112% | |
1949 | POSITIVE REGULATION OF KERATINOCYTE DIFFERENTIATION | 27 | -0.37 | -1.09 | 0.365 | 0.773 | 1.000 | 14790 | tags=48%, list=27%, signal=66% | |
1950 | RESPONSE TO PEPTIDE HORMONE | 1044 | -0.25 | -1.09 | 0.322 | 0.773 | 1.000 | 25186 | tags=51%, list=46%, signal=92% | |
1951 | NEGATIVE REGULATION OF GLIAL CELL PROLIFERATION | 18 | -0.36 | -1.09 | 0.340 | 0.773 | 1.000 | 6207 | tags=28%, list=11%, signal=31% | |
1952 | CELLULAR RESPONSE TO INSULIN STIMULUS | 824 | -0.26 | -1.09 | 0.275 | 0.773 | 1.000 | 26842 | tags=56%, list=49%, signal=108% | |
1953 | AMINO-ACID BETAINE METABOLIC PROCESS | 22 | -0.35 | -1.09 | 0.387 | 0.773 | 1.000 | 29840 | tags=77%, list=55%, signal=170% | |
1954 | PEPTIDYL-LYSINE MONOMETHYLATION | 16 | -0.38 | -1.09 | 0.385 | 0.773 | 1.000 | 26107 | tags=75%, list=48%, signal=143% | |
1955 | NEGATIVE REGULATION OF PROTEIN TYROSINE KINASE ACTIVITY | 34 | -0.33 | -1.09 | 0.357 | 0.773 | 1.000 | 27602 | tags=68%, list=50%, signal=137% | |
1956 | CARDIAC SEPTUM MORPHOGENESIS | 80 | -0.29 | -1.09 | 0.378 | 0.773 | 1.000 | 23708 | tags=50%, list=43%, signal=88% | |
1957 | INACTIVATION OF MAPK ACTIVITY | 39 | -0.35 | -1.09 | 0.390 | 0.773 | 1.000 | 24556 | tags=59%, list=45%, signal=107% | |
1958 | DNA-DEPENDENT DNA REPLICATION | 154 | -0.29 | -1.09 | 0.362 | 0.773 | 1.000 | 23228 | tags=53%, list=42%, signal=92% | |
1959 | NEGATIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY BY P53 CLASS MEDIATOR | 30 | -0.37 | -1.09 | 0.389 | 0.774 | 1.000 | 25657 | tags=70%, list=47%, signal=132% | |
1960 | CELLULAR AMINO ACID CATABOLIC PROCESS | 218 | -0.27 | -1.09 | 0.359 | 0.774 | 1.000 | 25109 | tags=54%, list=46%, signal=99% | |
1961 | NEGATIVE REGULATION OF ANION TRANSMEMBRANE TRANSPORT | 17 | -0.38 | -1.09 | 0.358 | 0.774 | 1.000 | 9287 | tags=35%, list=17%, signal=43% | |
1962 | REGULATION OF PHOSPHOLIPID CATABOLIC PROCESS | 17 | -0.39 | -1.09 | 0.366 | 0.774 | 1.000 | 19183 | tags=47%, list=35%, signal=72% | |
1963 | NUCLEAR PORE COMPLEX ASSEMBLY | 15 | -0.44 | -1.09 | 0.380 | 0.774 | 1.000 | 23874 | tags=80%, list=44%, signal=142% | |
1964 | REGULATION OF HISTONE METHYLATION | 91 | -0.32 | -1.09 | 0.362 | 0.774 | 1.000 | 15797 | tags=43%, list=29%, signal=60% | |
1965 | ZYMOGEN ACTIVATION | 246 | -0.29 | -1.09 | 0.381 | 0.773 | 1.000 | 22215 | tags=53%, list=41%, signal=89% | |
1966 | REGULATION OF ATRIAL CARDIAC MUSCLE CELL MEMBRANE REPOLARIZATION | 9 | -0.42 | -1.09 | 0.348 | 0.774 | 1.000 | 15903 | tags=44%, list=29%, signal=63% | |
1967 | FC RECEPTOR SIGNALING PATHWAY | 1037 | -0.25 | -1.09 | 0.321 | 0.773 | 1.000 | 26876 | tags=54%, list=49%, signal=104% | |
1968 | PLUS-END-DIRECTED VESICLE TRANSPORT ALONG MICROTUBULE | 13 | -0.42 | -1.09 | 0.388 | 0.774 | 1.000 | 31659 | tags=100%, list=58%, signal=237% | |
1969 | PLUS-END-DIRECTED ORGANELLE TRANSPORT ALONG MICROTUBULE | 13 | -0.42 | -1.09 | 0.388 | 0.773 | 1.000 | 31659 | tags=100%, list=58%, signal=237% | |
1970 | NEGATIVE REGULATION OF MEIOTIC CELL CYCLE | 13 | -0.43 | -1.09 | 0.382 | 0.773 | 1.000 | 15607 | tags=54%, list=29%, signal=75% | |
1971 | PULMONARY VALVE DEVELOPMENT | 21 | -0.35 | -1.09 | 0.364 | 0.773 | 1.000 | 25051 | tags=57%, list=46%, signal=105% | |
1972 | PULMONARY VALVE MORPHOGENESIS | 21 | -0.35 | -1.09 | 0.364 | 0.773 | 1.000 | 25051 | tags=57%, list=46%, signal=105% | |
1973 | CELLULAR RESPONSE TO STEROID HORMONE STIMULUS | 142 | -0.27 | -1.09 | 0.325 | 0.772 | 1.000 | 21268 | tags=45%, list=39%, signal=74% | |
1974 | PHOSPHATIDYLINOSITOL DEPHOSPHORYLATION | 33 | -0.37 | -1.09 | 0.403 | 0.772 | 1.000 | 28707 | tags=76%, list=53%, signal=159% | |
1975 | REGULATION OF NEURON DEATH | 260 | -0.28 | -1.09 | 0.364 | 0.772 | 1.000 | 26505 | tags=58%, list=48%, signal=112% | |
1976 | REGULATION OF VIRAL-INDUCED CYTOPLASMIC PATTERN RECOGNITION RECEPTOR SIGNALING PATHWAY | 27 | -0.34 | -1.09 | 0.396 | 0.772 | 1.000 | 5285 | tags=26%, list=10%, signal=29% | |
1977 | PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR SIGNALING PATHWAY | 11 | -0.42 | -1.09 | 0.373 | 0.772 | 1.000 | 25692 | tags=82%, list=47%, signal=154% | |
1978 | MORPHOGENESIS OF AN EPITHELIAL SHEET | 48 | -0.30 | -1.09 | 0.355 | 0.772 | 1.000 | 10215 | tags=29%, list=19%, signal=36% | |
1979 | REGULATION OF EPITHELIAL CELL DIFFERENTIATION INVOLVED IN KIDNEY DEVELOPMENT | 31 | -0.35 | -1.09 | 0.392 | 0.772 | 1.000 | 19886 | tags=52%, list=36%, signal=81% | |
1980 | T CELL DIFFERENTIATION IN THYMUS | 21 | -0.38 | -1.09 | 0.341 | 0.771 | 1.000 | 10975 | tags=38%, list=20%, signal=48% | |
1981 | THYMOCYTE AGGREGATION | 21 | -0.38 | -1.09 | 0.341 | 0.771 | 1.000 | 10975 | tags=38%, list=20%, signal=48% | |
1982 | TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 293 | -0.29 | -1.09 | 0.352 | 0.771 | 1.000 | 20835 | tags=49%, list=38%, signal=80% | |
1983 | LIPID BIOSYNTHETIC PROCESS | 928 | -0.28 | -1.09 | 0.241 | 0.771 | 1.000 | 24487 | tags=55%, list=45%, signal=97% | |
1984 | POSITIVE REGULATION OF INTRACELLULAR STEROID HORMONE RECEPTOR SIGNALING PATHWAY | 25 | -0.35 | -1.09 | 0.365 | 0.771 | 1.000 | 22488 | tags=52%, list=41%, signal=88% | |
1985 | REGULATION OF INTRACELLULAR ESTROGEN RECEPTOR SIGNALING PATHWAY | 58 | -0.32 | -1.09 | 0.360 | 0.771 | 1.000 | 28324 | tags=64%, list=52%, signal=132% | |
1986 | REGULATION OF COFACTOR METABOLIC PROCESS | 97 | -0.32 | -1.09 | 0.418 | 0.772 | 1.000 | 24473 | tags=60%, list=45%, signal=108% | |
1987 | REGULATION OF COENZYME METABOLIC PROCESS | 97 | -0.32 | -1.09 | 0.418 | 0.771 | 1.000 | 24473 | tags=60%, list=45%, signal=108% | |
1988 | POSITIVE REGULATION OF ODONTOGENESIS | 11 | -0.43 | -1.09 | 0.358 | 0.771 | 1.000 | 24638 | tags=64%, list=45%, signal=116% | |
1989 | NEGATIVE REGULATION OF INTRACELLULAR ESTROGEN RECEPTOR SIGNALING PATHWAY | 26 | -0.33 | -1.09 | 0.360 | 0.771 | 1.000 | 26978 | tags=65%, list=49%, signal=129% | |
1990 | PYRIMIDINE NUCLEOTIDE-SUGAR TRANSMEMBRANE TRANSPORT | 11 | -0.45 | -1.09 | 0.392 | 0.771 | 1.000 | 16715 | tags=64%, list=31%, signal=92% | |
1991 | DETECTION OF BACTERIUM | 26 | -0.39 | -1.09 | 0.411 | 0.771 | 1.000 | 22804 | tags=65%, list=42%, signal=112% | |
1992 | DETECTION OF OTHER ORGANISM | 26 | -0.39 | -1.09 | 0.411 | 0.770 | 1.000 | 22804 | tags=65%, list=42%, signal=112% | |
1993 | ANTIGEN PROCESSING AND PRESENTATION OF PEPTIDE ANTIGEN VIA MHC CLASS II | 213 | -0.29 | -1.09 | 0.381 | 0.770 | 1.000 | 23401 | tags=54%, list=43%, signal=95% | |
1994 | ANTIGEN PROCESSING AND PRESENTATION OF PEPTIDE OR POLYSACCHARIDE ANTIGEN VIA MHC CLASS II | 213 | -0.29 | -1.09 | 0.381 | 0.770 | 1.000 | 23401 | tags=54%, list=43%, signal=95% | |
1995 | POSITIVE REGULATION OF COLLAGEN METABOLIC PROCESS | 19 | -0.36 | -1.09 | 0.403 | 0.770 | 1.000 | 14822 | tags=37%, list=27%, signal=51% | |
1996 | POSITIVE REGULATION OF COLLAGEN BIOSYNTHETIC PROCESS | 19 | -0.36 | -1.09 | 0.403 | 0.770 | 1.000 | 14822 | tags=37%, list=27%, signal=51% | |
1997 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 19 | -0.36 | -1.09 | 0.403 | 0.769 | 1.000 | 14822 | tags=37%, list=27%, signal=51% | |
1998 | CELLULAR RESPONSE TO ALKALOID | 37 | -0.33 | -1.09 | 0.375 | 0.769 | 1.000 | 19314 | tags=41%, list=35%, signal=63% | |
1999 | REGULATION OF I-KAPPAB KINASE/NF-KAPPAB SIGNALING | 481 | -0.29 | -1.08 | 0.468 | 0.769 | 1.000 | 25677 | tags=58%, list=47%, signal=109% | |
2000 | RESPONSE TO PEPTIDE | 1070 | -0.25 | -1.08 | 0.341 | 0.770 | 1.000 | 25186 | tags=51%, list=46%, signal=92% | |
2001 | NEGATIVE REGULATION OF ENDOCYTOSIS | 67 | -0.33 | -1.08 | 0.394 | 0.769 | 1.000 | 17547 | tags=46%, list=32%, signal=68% | |
2002 | NEGATIVE REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 46 | -0.32 | -1.08 | 0.377 | 0.769 | 1.000 | 17225 | tags=43%, list=32%, signal=63% | |
2003 | PYRIMIDINE NUCLEOBASE METABOLIC PROCESS | 57 | -0.32 | -1.08 | 0.389 | 0.769 | 1.000 | 28039 | tags=70%, list=51%, signal=144% | |
2004 | DEFINITIVE HEMOPOIESIS | 16 | -0.36 | -1.08 | 0.354 | 0.769 | 1.000 | 12775 | tags=38%, list=23%, signal=49% | |
2005 | RESPONSE TO NUTRIENT LEVELS | 286 | -0.29 | -1.08 | 0.297 | 0.769 | 1.000 | 27797 | tags=64%, list=51%, signal=129% | |
2006 | MORPHOGENESIS OF EMBRYONIC EPITHELIUM | 104 | -0.28 | -1.08 | 0.377 | 0.769 | 1.000 | 17093 | tags=40%, list=31%, signal=59% | |
2007 | COENZYME TRANSPORT | 10 | -0.41 | -1.08 | 0.364 | 0.769 | 1.000 | 31864 | tags=80%, list=58%, signal=192% | |
2008 | HISTONE ARGININE METHYLATION | 20 | -0.38 | -1.08 | 0.399 | 0.769 | 1.000 | 26114 | tags=75%, list=48%, signal=144% | |
2009 | REGULATION OF RESPONSE TO DNA DAMAGE STIMULUS | 309 | -0.28 | -1.08 | 0.331 | 0.769 | 1.000 | 29142 | tags=64%, list=53%, signal=136% | |
2010 | SYNAPTONEMAL COMPLEX ASSEMBLY | 10 | -0.45 | -1.08 | 0.379 | 0.769 | 1.000 | 5264 | tags=30%, list=10%, signal=33% | |
2011 | SYNAPTONEMAL COMPLEX ORGANIZATION | 10 | -0.45 | -1.08 | 0.379 | 0.768 | 1.000 | 5264 | tags=30%, list=10%, signal=33% | |
2012 | POSITIVE REGULATION OF LEUKOCYTE MEDIATED IMMUNITY | 114 | -0.29 | -1.08 | 0.362 | 0.768 | 1.000 | 17597 | tags=41%, list=32%, signal=61% | |
2013 | RNA LOCALIZATION | 225 | -0.31 | -1.08 | 0.400 | 0.769 | 1.000 | 23917 | tags=58%, list=44%, signal=102% | |
2014 | NEUROBLAST PROLIFERATION | 41 | -0.32 | -1.08 | 0.345 | 0.769 | 1.000 | 15718 | tags=41%, list=29%, signal=58% | |
2015 | TISSUE REGENERATION | 36 | -0.35 | -1.08 | 0.403 | 0.769 | 1.000 | 18711 | tags=50%, list=34%, signal=76% | |
2016 | RESPONSE TO PH | 32 | -0.31 | -1.08 | 0.355 | 0.769 | 1.000 | 33277 | tags=81%, list=61%, signal=207% | |
2017 | WATER-SOLUBLE VITAMIN METABOLIC PROCESS | 217 | -0.29 | -1.08 | 0.355 | 0.769 | 1.000 | 19714 | tags=45%, list=36%, signal=70% | |
2018 | NEGATIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 316 | -0.29 | -1.08 | 0.386 | 0.769 | 1.000 | 20002 | tags=46%, list=37%, signal=72% | |
2019 | TRANSCYTOSIS | 11 | -0.41 | -1.08 | 0.380 | 0.769 | 1.000 | 23806 | tags=64%, list=44%, signal=113% | |
2020 | RESPONSE TO INTERLEUKIN-3 | 10 | -0.40 | -1.08 | 0.359 | 0.768 | 1.000 | 19317 | tags=50%, list=35%, signal=77% | |
2021 | CELLULAR RESPONSE TO INTERLEUKIN-3 | 10 | -0.40 | -1.08 | 0.359 | 0.768 | 1.000 | 19317 | tags=50%, list=35%, signal=77% | |
2022 | MEMBRANE PROTEIN PROTEOLYSIS | 89 | -0.31 | -1.08 | 0.403 | 0.769 | 1.000 | 25629 | tags=62%, list=47%, signal=116% | |
2023 | INOSITOL PHOSPHATE-MEDIATED SIGNALING | 40 | -0.31 | -1.08 | 0.348 | 0.768 | 1.000 | 9654 | tags=28%, list=18%, signal=33% | |
2024 | NEGATIVE REGULATION OF CATION TRANSMEMBRANE TRANSPORT | 105 | -0.27 | -1.08 | 0.370 | 0.768 | 1.000 | 20611 | tags=45%, list=38%, signal=72% | |
2025 | PYRIMIDINE NUCLEOTIDE BIOSYNTHETIC PROCESS | 13 | -0.42 | -1.08 | 0.370 | 0.768 | 1.000 | 20054 | tags=62%, list=37%, signal=97% | |
2026 | REGULATION OF TUMOR NECROSIS FACTOR-MEDIATED SIGNALING PATHWAY | 94 | -0.30 | -1.08 | 0.425 | 0.768 | 1.000 | 10457 | tags=33%, list=19%, signal=41% | |
2027 | REGULATION OF HISTONE PHOSPHORYLATION | 15 | -0.37 | -1.08 | 0.351 | 0.768 | 1.000 | 6831 | tags=33%, list=12%, signal=38% | |
2028 | REGULATION OF CYSTEINE-TYPE ENDOPEPTIDASE ACTIVITY | 472 | -0.28 | -1.08 | 0.398 | 0.768 | 1.000 | 21279 | tags=50%, list=39%, signal=81% | |
2029 | DEVELOPMENTAL INDUCTION | 15 | -0.37 | -1.08 | 0.361 | 0.767 | 1.000 | 6904 | tags=27%, list=13%, signal=31% | |
2030 | STRESS-ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 255 | -0.29 | -1.08 | 0.381 | 0.767 | 1.000 | 25616 | tags=58%, list=47%, signal=109% | |
2031 | REGULATION OF ANDROGEN RECEPTOR SIGNALING PATHWAY | 72 | -0.30 | -1.08 | 0.391 | 0.767 | 1.000 | 28737 | tags=67%, list=53%, signal=140% | |
2032 | NUCLEAR TRANSPORT | 450 | -0.30 | -1.08 | 0.413 | 0.768 | 1.000 | 27143 | tags=63%, list=50%, signal=124% | |
2033 | NEGATIVE REGULATION OF DENDRITE DEVELOPMENT | 38 | -0.35 | -1.08 | 0.382 | 0.767 | 1.000 | 26579 | tags=71%, list=49%, signal=138% | |
2034 | SPLEEN DEVELOPMENT | 15 | -0.37 | -1.08 | 0.372 | 0.768 | 1.000 | 7025 | tags=33%, list=13%, signal=38% | |
2035 | POSITIVE REGULATION OF TRIGLYCERIDE CATABOLIC PROCESS | 14 | -0.41 | -1.08 | 0.397 | 0.768 | 1.000 | 6134 | tags=29%, list=11%, signal=32% | |
2036 | REGULATION OF CALCINEURIN-NFAT SIGNALING CASCADE | 28 | -0.35 | -1.08 | 0.351 | 0.768 | 1.000 | 22671 | tags=57%, list=41%, signal=98% | |
2037 | ATF6-MEDIATED UNFOLDED PROTEIN RESPONSE | 26 | -0.36 | -1.08 | 0.402 | 0.769 | 1.000 | 20293 | tags=58%, list=37%, signal=92% | |
2038 | REGULATION OF VESICLE-MEDIATED TRANSPORT | 604 | -0.26 | -1.08 | 0.364 | 0.768 | 1.000 | 17066 | tags=38%, list=31%, signal=55% | |
2039 | HORMONE-MEDIATED SIGNALING PATHWAY | 99 | -0.27 | -1.08 | 0.343 | 0.769 | 1.000 | 23466 | tags=47%, list=43%, signal=83% | |
2040 | NEPHRON TUBULE FORMATION | 20 | -0.37 | -1.08 | 0.357 | 0.769 | 1.000 | 17093 | tags=45%, list=31%, signal=65% | |
2041 | NEGATIVE REGULATION OF INTRACELLULAR TRANSPORT | 270 | -0.26 | -1.08 | 0.338 | 0.769 | 1.000 | 23310 | tags=48%, list=43%, signal=84% | |
2042 | IMMUNE RESPONSE-REGULATING CELL SURFACE RECEPTOR SIGNALING PATHWAY INVOLVED IN PHAGOCYTOSIS | 282 | -0.27 | -1.08 | 0.352 | 0.769 | 1.000 | 23149 | tags=48%, list=42%, signal=82% | |
2043 | FC-GAMMA RECEPTOR SIGNALING PATHWAY | 282 | -0.27 | -1.08 | 0.352 | 0.769 | 1.000 | 23149 | tags=48%, list=42%, signal=82% | |
2044 | FC-GAMMA RECEPTOR SIGNALING PATHWAY INVOLVED IN PHAGOCYTOSIS | 282 | -0.27 | -1.08 | 0.352 | 0.768 | 1.000 | 23149 | tags=48%, list=42%, signal=82% | |
2045 | REGULATION OF PROTEIN COMPLEX ASSEMBLY | 564 | -0.27 | -1.08 | 0.321 | 0.768 | 1.000 | 19479 | tags=44%, list=36%, signal=67% | |
2046 | NEGATIVE REGULATION OF DNA-TEMPLATED TRANSCRIPTION, ELONGATION | 13 | -0.37 | -1.08 | 0.374 | 0.768 | 1.000 | 13982 | tags=38%, list=26%, signal=52% | |
2047 | STEROL TRANSPORT | 88 | -0.29 | -1.08 | 0.378 | 0.768 | 1.000 | 21720 | tags=47%, list=40%, signal=77% | |
2048 | REGULATION OF ALPHA-BETA T CELL PROLIFERATION | 22 | -0.42 | -1.08 | 0.404 | 0.768 | 1.000 | 25520 | tags=77%, list=47%, signal=145% | |
2049 | REGULATION OF STEM CELL DIFFERENTIATION | 257 | -0.27 | -1.08 | 0.367 | 0.768 | 1.000 | 22858 | tags=47%, list=42%, signal=81% | |
2050 | PROTEIN TARGETING TO VACUOLE | 43 | -0.34 | -1.08 | 0.403 | 0.768 | 1.000 | 13729 | tags=42%, list=25%, signal=56% | |
2051 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO VACUOLE | 43 | -0.34 | -1.08 | 0.403 | 0.767 | 1.000 | 13729 | tags=42%, list=25%, signal=56% | |
2052 | RESPONSE TO INSULIN | 840 | -0.26 | -1.08 | 0.292 | 0.767 | 1.000 | 26842 | tags=55%, list=49%, signal=107% | |
2053 | ADRENERGIC RECEPTOR SIGNALING PATHWAY | 39 | -0.32 | -1.08 | 0.395 | 0.767 | 1.000 | 12581 | tags=33%, list=23%, signal=43% | |
2054 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 298 | -0.28 | -1.08 | 0.385 | 0.767 | 1.000 | 18905 | tags=43%, list=35%, signal=65% | |
2055 | REGULATION OF FAT CELL PROLIFERATION | 15 | -0.39 | -1.08 | 0.356 | 0.767 | 1.000 | 24049 | tags=60%, list=44%, signal=107% | |
2056 | PEROXISOMAL MEMBRANE TRANSPORT | 13 | -0.42 | -1.08 | 0.420 | 0.767 | 1.000 | 23400 | tags=77%, list=43%, signal=134% | |
2057 | PROTEIN IMPORT INTO PEROXISOME MEMBRANE | 13 | -0.42 | -1.08 | 0.420 | 0.766 | 1.000 | 23400 | tags=77%, list=43%, signal=134% | |
2058 | RESPONSE TO EXTRACELLULAR STIMULUS | 302 | -0.28 | -1.08 | 0.330 | 0.766 | 1.000 | 27797 | tags=62%, list=51%, signal=126% | |
2059 | SULFUR AMINO ACID METABOLIC PROCESS | 78 | -0.29 | -1.08 | 0.356 | 0.767 | 1.000 | 27293 | tags=64%, list=50%, signal=128% | |
2060 | REGULATION OF CIRCADIAN RHYTHM | 221 | -0.27 | -1.08 | 0.364 | 0.767 | 1.000 | 19060 | tags=43%, list=35%, signal=65% | |
2061 | SPERMATID DIFFERENTIATION | 86 | -0.26 | -1.08 | 0.344 | 0.767 | 1.000 | 21263 | tags=44%, list=39%, signal=72% | |
2062 | EPITHELIAL TO MESENCHYMAL TRANSITION INVOLVED IN ENDOCARDIAL CUSHION FORMATION | 11 | -0.39 | -1.08 | 0.366 | 0.767 | 1.000 | 25051 | tags=64%, list=46%, signal=117% | |
2063 | REGULATION OF NIK/NF-KAPPAB SIGNALING | 51 | -0.31 | -1.08 | 0.369 | 0.767 | 1.000 | 23080 | tags=57%, list=42%, signal=98% | |
2064 | GLYCEROLIPID CATABOLIC PROCESS | 71 | -0.29 | -1.08 | 0.355 | 0.767 | 1.000 | 23759 | tags=54%, list=43%, signal=95% | |
2065 | DNA DOUBLE-STRAND BREAK PROCESSING | 24 | -0.36 | -1.08 | 0.380 | 0.767 | 1.000 | 26060 | tags=67%, list=48%, signal=127% | |
2066 | MIRNA LOADING ONTO RISC INVOLVED IN GENE SILENCING BY MIRNA | 18 | -0.38 | -1.08 | 0.408 | 0.769 | 1.000 | 13082 | tags=44%, list=24%, signal=58% | |
2067 | NUCLEOSOME ORGANIZATION | 202 | -0.29 | -1.08 | 0.322 | 0.769 | 1.000 | 19992 | tags=47%, list=37%, signal=73% | |
2068 | PROTEIN POLYGLUTAMYLATION | 13 | -0.40 | -1.08 | 0.393 | 0.768 | 1.000 | 16919 | tags=54%, list=31%, signal=78% | |
2069 | POSITIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 203 | -0.28 | -1.08 | 0.387 | 0.768 | 1.000 | 29089 | tags=64%, list=53%, signal=135% | |
2070 | ACYLGLYCEROL ACYL-CHAIN REMODELING | 10 | -0.45 | -1.08 | 0.382 | 0.769 | 1.000 | 7336 | tags=30%, list=13%, signal=35% | |
2071 | POSITIVE REGULATION OF TOLL-LIKE RECEPTOR 4 SIGNALING PATHWAY | 18 | -0.37 | -1.08 | 0.377 | 0.769 | 1.000 | 19428 | tags=50%, list=36%, signal=78% | |
2072 | RESPONSE TO UV | 236 | -0.28 | -1.08 | 0.403 | 0.769 | 1.000 | 18526 | tags=45%, list=34%, signal=68% | |
2073 | PLASMA LIPOPROTEIN PARTICLE ASSEMBLY | 28 | -0.34 | -1.08 | 0.374 | 0.769 | 1.000 | 24670 | tags=57%, list=45%, signal=104% | |
2074 | NEGATIVE REGULATION OF HYDROGEN PEROXIDE-MEDIATED PROGRAMMED CELL DEATH | 14 | -0.37 | -1.07 | 0.372 | 0.769 | 1.000 | 6843 | tags=29%, list=13%, signal=33% | |
2075 | L-ALPHA-AMINO ACID TRANSMEMBRANE TRANSPORT | 55 | -0.30 | -1.07 | 0.374 | 0.769 | 1.000 | 21995 | tags=51%, list=40%, signal=85% | |
2076 | LIVER DEVELOPMENT | 56 | -0.31 | -1.07 | 0.387 | 0.770 | 1.000 | 22928 | tags=55%, list=42%, signal=95% | |
2077 | POSITIVE REGULATION OF SYNAPTIC TRANSMISSION, GLUTAMATERGIC | 23 | -0.34 | -1.07 | 0.395 | 0.770 | 1.000 | 7877 | tags=26%, list=14%, signal=30% | |
2078 | POSTREPLICATION REPAIR | 104 | -0.33 | -1.07 | 0.410 | 0.770 | 1.000 | 17205 | tags=49%, list=31%, signal=71% | |
2079 | ATP HYDROLYSIS COUPLED TRANSMEMBRANE TRANSPORT | 15 | -0.39 | -1.07 | 0.389 | 0.771 | 1.000 | 16903 | tags=53%, list=31%, signal=77% | |
2080 | DNA DAMAGE RESPONSE, DETECTION OF DNA DAMAGE | 72 | -0.32 | -1.07 | 0.410 | 0.771 | 1.000 | 16098 | tags=44%, list=29%, signal=63% | |
2081 | NEGATIVE REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 19 | -0.38 | -1.07 | 0.404 | 0.772 | 1.000 | 22943 | tags=68%, list=42%, signal=118% | |
2082 | NUCLEOTIDE-SUGAR TRANSPORT | 14 | -0.43 | -1.07 | 0.415 | 0.772 | 1.000 | 18271 | tags=64%, list=33%, signal=97% | |
2083 | PYRIMIDINE NUCLEOTIDE-SUGAR TRANSPORT | 14 | -0.43 | -1.07 | 0.415 | 0.772 | 1.000 | 18271 | tags=64%, list=33%, signal=97% | |
2084 | NEUTRAL LIPID METABOLIC PROCESS | 203 | -0.26 | -1.07 | 0.366 | 0.772 | 1.000 | 24351 | tags=52%, list=45%, signal=93% | |
2085 | ACYLGLYCEROL METABOLIC PROCESS | 203 | -0.26 | -1.07 | 0.366 | 0.771 | 1.000 | 24351 | tags=52%, list=45%, signal=93% | |
2086 | NEGATIVE REGULATION OF MITOCHONDRION ORGANIZATION | 75 | -0.29 | -1.07 | 0.387 | 0.771 | 1.000 | 7085 | tags=27%, list=13%, signal=31% | |
2087 | REGULATION OF RECEPTOR INTERNALIZATION | 65 | -0.31 | -1.07 | 0.406 | 0.772 | 1.000 | 15405 | tags=42%, list=28%, signal=58% | |
2088 | PROTEIN IMPORT INTO PEROXISOME MATRIX | 27 | -0.37 | -1.07 | 0.408 | 0.772 | 1.000 | 32745 | tags=93%, list=60%, signal=231% | |
2089 | CALCIUM-DEPENDENT CELL-CELL ADHESION VIA PLASMA MEMBRANE CELL ADHESION MOLECULES | 14 | -0.40 | -1.07 | 0.387 | 0.772 | 1.000 | 10141 | tags=36%, list=19%, signal=44% | |
2090 | ACTIN POLYMERIZATION OR DEPOLYMERIZATION | 64 | -0.31 | -1.07 | 0.377 | 0.771 | 1.000 | 19891 | tags=50%, list=36%, signal=79% | |
2091 | POSITIVE REGULATION OF NATURAL KILLER CELL MEDIATED CYTOTOXICITY | 35 | -0.32 | -1.07 | 0.395 | 0.771 | 1.000 | 16819 | tags=43%, list=31%, signal=62% | |
2092 | POSITIVE REGULATION OF CYCLIN-DEPENDENT PROTEIN SERINE/THREONINE KINASE ACTIVITY | 57 | -0.27 | -1.07 | 0.377 | 0.771 | 1.000 | 15550 | tags=35%, list=28%, signal=49% | |
2093 | POSITIVE REGULATION OF CAMP-MEDIATED SIGNALING | 33 | -0.34 | -1.07 | 0.375 | 0.771 | 1.000 | 16270 | tags=36%, list=30%, signal=52% | |
2094 | REGULATION OF INTRACELLULAR TRANSPORT | 1152 | -0.26 | -1.07 | 0.322 | 0.771 | 1.000 | 26192 | tags=54%, list=48%, signal=101% | |
2095 | POSITIVE REGULATION BY HOST OF VIRAL TRANSCRIPTION | 36 | -0.34 | -1.07 | 0.397 | 0.771 | 1.000 | 32968 | tags=81%, list=60%, signal=203% | |
2096 | MANGANESE ION TRANSPORT | 17 | -0.38 | -1.07 | 0.400 | 0.771 | 1.000 | 10141 | tags=41%, list=19%, signal=51% | |
2097 | POSITIVE REGULATION OF CELL KILLING | 64 | -0.31 | -1.07 | 0.420 | 0.770 | 1.000 | 17332 | tags=42%, list=32%, signal=62% | |
2098 | CELLULAR SODIUM ION HOMEOSTASIS | 27 | -0.34 | -1.07 | 0.390 | 0.771 | 1.000 | 17609 | tags=41%, list=32%, signal=60% | |
2099 | REGULATION OF CARDIAC MUSCLE CELL MEMBRANE POTENTIAL | 14 | -0.37 | -1.07 | 0.361 | 0.771 | 1.000 | 16636 | tags=43%, list=30%, signal=62% | |
2100 | SYNAPTIC VESICLE CYCLE | 64 | -0.29 | -1.07 | 0.369 | 0.770 | 1.000 | 16426 | tags=38%, list=30%, signal=54% | |
2101 | NUCLEOCYTOPLASMIC TRANSPORT | 441 | -0.30 | -1.07 | 0.423 | 0.770 | 1.000 | 22692 | tags=54%, list=42%, signal=91% | |
2102 | NEGATIVE REGULATION OF CALCIUM ION TRANSPORT | 79 | -0.27 | -1.07 | 0.381 | 0.770 | 1.000 | 19547 | tags=42%, list=36%, signal=65% | |
2103 | UV-DAMAGE EXCISION REPAIR | 15 | -0.41 | -1.07 | 0.414 | 0.770 | 1.000 | 32199 | tags=100%, list=59%, signal=243% | |
2104 | STRESS-ACTIVATED MAPK CASCADE | 252 | -0.29 | -1.07 | 0.392 | 0.770 | 1.000 | 25616 | tags=58%, list=47%, signal=109% | |
2105 | GMP METABOLIC PROCESS | 33 | -0.34 | -1.07 | 0.409 | 0.771 | 1.000 | 20481 | tags=55%, list=37%, signal=87% | |
2106 | POSITIVE REGULATION OF PROTEIN IMPORT | 178 | -0.28 | -1.07 | 0.389 | 0.771 | 1.000 | 29089 | tags=63%, list=53%, signal=134% | |
2107 | CYTOPLASMIC PATTERN RECOGNITION RECEPTOR SIGNALING PATHWAY | 75 | -0.34 | -1.07 | 0.425 | 0.771 | 1.000 | 25045 | tags=65%, list=46%, signal=120% | |
2108 | REGULATION OF ENDOCYTOSIS | 336 | -0.27 | -1.07 | 0.359 | 0.771 | 1.000 | 16866 | tags=38%, list=31%, signal=54% | |
2109 | POSITIVE REGULATION OF SECRETION BY CELL | 413 | -0.26 | -1.07 | 0.366 | 0.770 | 1.000 | 23143 | tags=48%, list=42%, signal=83% | |
2110 | TOLL-LIKE RECEPTOR 4 SIGNALING PATHWAY | 255 | -0.30 | -1.07 | 0.443 | 0.770 | 1.000 | 25375 | tags=58%, list=46%, signal=108% | |
2111 | MODIFICATION OF MORPHOLOGY OR PHYSIOLOGY OF OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 251 | -0.30 | -1.07 | 0.357 | 0.770 | 1.000 | 22221 | tags=53%, list=41%, signal=89% | |
2112 | NEGATIVE REGULATION OF ATPASE ACTIVITY | 19 | -0.37 | -1.07 | 0.400 | 0.770 | 1.000 | 16906 | tags=47%, list=31%, signal=69% | |
2113 | REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 522 | -0.25 | -1.07 | 0.383 | 0.770 | 1.000 | 19530 | tags=42%, list=36%, signal=65% | |
2114 | POSITIVE REGULATION OF CALCIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 55 | -0.28 | -1.07 | 0.348 | 0.770 | 1.000 | 22928 | tags=51%, list=42%, signal=88% | |
2115 | BONE DEVELOPMENT | 146 | -0.26 | -1.07 | 0.345 | 0.770 | 1.000 | 19782 | tags=39%, list=36%, signal=61% | |
2116 | TOLL-LIKE RECEPTOR SIGNALING PATHWAY | 308 | -0.29 | -1.07 | 0.467 | 0.771 | 1.000 | 25375 | tags=58%, list=46%, signal=108% | |
2117 | MITOPHAGY IN RESPONSE TO MITOCHONDRIAL DEPOLARIZATION | 286 | -0.26 | -1.07 | 0.369 | 0.771 | 1.000 | 14229 | tags=34%, list=26%, signal=46% | |
2118 | RESPONSE TO MITOCHONDRIAL DEPOLARISATION | 286 | -0.26 | -1.07 | 0.369 | 0.770 | 1.000 | 14229 | tags=34%, list=26%, signal=46% | |
2119 | REGULATION OF CHEMOKINE (C-X-C MOTIF) LIGAND 2 PRODUCTION | 16 | -0.37 | -1.07 | 0.389 | 0.770 | 1.000 | 19583 | tags=50%, list=36%, signal=78% | |
2120 | WATER TRANSPORT | 86 | -0.26 | -1.07 | 0.362 | 0.770 | 1.000 | 15963 | tags=34%, list=29%, signal=48% | |
2121 | SCHWANN CELL DIFFERENTIATION | 37 | -0.33 | -1.07 | 0.363 | 0.770 | 1.000 | 25937 | tags=68%, list=47%, signal=128% | |
2122 | CELL FATE SPECIFICATION | 43 | -0.29 | -1.07 | 0.376 | 0.770 | 1.000 | 27298 | tags=60%, list=50%, signal=121% | |
2123 | ANTIGEN PROCESSING AND PRESENTATION OF EXOGENOUS PEPTIDE ANTIGEN VIA MHC CLASS II | 209 | -0.29 | -1.07 | 0.405 | 0.770 | 1.000 | 23401 | tags=54%, list=43%, signal=94% | |
2124 | POSITIVE REGULATION OF CYCLIN-DEPENDENT PROTEIN KINASE ACTIVITY | 60 | -0.27 | -1.07 | 0.376 | 0.770 | 1.000 | 18365 | tags=40%, list=34%, signal=60% | |
2125 | MEMBRANE RAFT ORGANIZATION | 36 | -0.35 | -1.07 | 0.396 | 0.770 | 1.000 | 20841 | tags=58%, list=38%, signal=94% | |
2126 | HEART VALVE DEVELOPMENT | 47 | -0.30 | -1.07 | 0.378 | 0.770 | 1.000 | 12962 | tags=34%, list=24%, signal=45% | |
2127 | HEART VALVE MORPHOGENESIS | 47 | -0.30 | -1.07 | 0.378 | 0.769 | 1.000 | 12962 | tags=34%, list=24%, signal=45% | |
2128 | LIPID TRANSPORT | 287 | -0.26 | -1.07 | 0.389 | 0.769 | 1.000 | 24104 | tags=51%, list=44%, signal=91% | |
2129 | MICROTUBULE CYTOSKELETON ORGANIZATION | 581 | -0.29 | -1.07 | 0.369 | 0.769 | 1.000 | 27719 | tags=63%, list=51%, signal=127% | |
2130 | POSITIVE REGULATION OF ORGANELLE ASSEMBLY | 89 | -0.30 | -1.07 | 0.398 | 0.769 | 1.000 | 24838 | tags=61%, list=45%, signal=111% | |
2131 | MICROTUBULE-BASED MOVEMENT | 246 | -0.29 | -1.07 | 0.414 | 0.769 | 1.000 | 25643 | tags=61%, list=47%, signal=114% | |
2132 | LYSOSOME ORGANIZATION | 89 | -0.30 | -1.07 | 0.391 | 0.769 | 1.000 | 27394 | tags=63%, list=50%, signal=126% | |
2133 | LYTIC VACUOLE ORGANIZATION | 89 | -0.30 | -1.07 | 0.391 | 0.769 | 1.000 | 27394 | tags=63%, list=50%, signal=126% | |
2134 | PYRIMIDINE NUCLEOSIDE METABOLIC PROCESS | 75 | -0.30 | -1.07 | 0.388 | 0.770 | 1.000 | 21380 | tags=55%, list=39%, signal=90% | |
2135 | PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 299 | -0.26 | -1.07 | 0.366 | 0.771 | 1.000 | 21400 | tags=45%, list=39%, signal=74% | |
2136 | PROTEIN LOCALIZATION TO CELL PERIPHERY | 299 | -0.26 | -1.07 | 0.366 | 0.771 | 1.000 | 21400 | tags=45%, list=39%, signal=74% | |
2137 | LONG-CHAIN FATTY-ACYL-COA METABOLIC PROCESS | 91 | -0.30 | -1.07 | 0.390 | 0.771 | 1.000 | 27232 | tags=63%, list=50%, signal=125% | |
2138 | REELIN-MEDIATED SIGNALING PATHWAY | 5 | -0.51 | -1.07 | 0.379 | 0.771 | 1.000 | 26891 | tags=100%, list=49%, signal=197% | |
2139 | ADHERENS JUNCTION ORGANIZATION | 171 | -0.27 | -1.07 | 0.382 | 0.771 | 1.000 | 15751 | tags=35%, list=29%, signal=49% | |
2140 | NEUTRAL AMINO ACID TRANSPORT | 41 | -0.30 | -1.07 | 0.374 | 0.771 | 1.000 | 23198 | tags=54%, list=42%, signal=93% | |
2141 | DOUBLE-STRAND BREAK REPAIR VIA NONHOMOLOGOUS END JOINING | 130 | -0.30 | -1.07 | 0.407 | 0.771 | 1.000 | 30398 | tags=70%, list=56%, signal=157% | |
2142 | PIGMENT METABOLIC PROCESS | 79 | -0.30 | -1.07 | 0.399 | 0.771 | 1.000 | 20481 | tags=49%, list=37%, signal=79% | |
2143 | POSITIVE REGULATION OF FILOPODIUM ASSEMBLY | 39 | -0.31 | -1.07 | 0.396 | 0.771 | 1.000 | 26811 | tags=56%, list=49%, signal=111% | |
2144 | CHOLESTEROL BIOSYNTHETIC PROCESS | 55 | -0.33 | -1.06 | 0.420 | 0.771 | 1.000 | 26011 | tags=67%, list=48%, signal=128% | |
2145 | SECONDARY ALCOHOL BIOSYNTHETIC PROCESS | 55 | -0.33 | -1.06 | 0.420 | 0.771 | 1.000 | 26011 | tags=67%, list=48%, signal=128% | |
2146 | NEGATIVE REGULATION OF DNA METABOLIC PROCESS | 251 | -0.28 | -1.06 | 0.374 | 0.771 | 1.000 | 23084 | tags=50%, list=42%, signal=86% | |
2147 | POSITIVE REGULATION OF EPIDERMAL CELL DIFFERENTIATION | 33 | -0.35 | -1.06 | 0.409 | 0.771 | 1.000 | 14790 | tags=45%, list=27%, signal=62% | |
2148 | MODIFICATION OF MORPHOLOGY OR PHYSIOLOGY OF OTHER ORGANISM | 255 | -0.29 | -1.06 | 0.368 | 0.771 | 1.000 | 22221 | tags=53%, list=41%, signal=88% | |
2149 | MACROPHAGE DIFFERENTIATION | 15 | -0.36 | -1.06 | 0.406 | 0.772 | 1.000 | 15714 | tags=47%, list=29%, signal=65% | |
2150 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE III PROMOTER | 31 | -0.32 | -1.06 | 0.402 | 0.771 | 1.000 | 30021 | tags=71%, list=55%, signal=157% | |
2151 | GOLGI ORGANIZATION | 193 | -0.31 | -1.06 | 0.418 | 0.771 | 1.000 | 26349 | tags=64%, list=48%, signal=123% | |
2152 | NEGATIVE REGULATION OF DNA REPAIR | 32 | -0.33 | -1.06 | 0.403 | 0.772 | 1.000 | 19300 | tags=50%, list=35%, signal=77% | |
2153 | MISMATCH REPAIR | 33 | -0.37 | -1.06 | 0.414 | 0.772 | 1.000 | 31392 | tags=88%, list=57%, signal=206% | |
2154 | REGULATION OF ATPASE ACTIVITY | 107 | -0.27 | -1.06 | 0.410 | 0.772 | 1.000 | 19532 | tags=44%, list=36%, signal=68% | |
2155 | RESPONSE TO CELL CYCLE CHECKPOINT SIGNALING | 10 | -0.44 | -1.06 | 0.389 | 0.772 | 1.000 | 18587 | tags=60%, list=34%, signal=91% | |
2156 | RESPONSE TO DNA INTEGRITY CHECKPOINT SIGNALING | 10 | -0.44 | -1.06 | 0.389 | 0.772 | 1.000 | 18587 | tags=60%, list=34%, signal=91% | |
2157 | RESPONSE TO DNA DAMAGE CHECKPOINT SIGNALING | 10 | -0.44 | -1.06 | 0.389 | 0.772 | 1.000 | 18587 | tags=60%, list=34%, signal=91% | |
2158 | LONG-CHAIN FATTY ACID METABOLIC PROCESS | 164 | -0.28 | -1.06 | 0.403 | 0.771 | 1.000 | 28804 | tags=66%, list=53%, signal=140% | |
2159 | PLATELET ACTIVATION | 590 | -0.26 | -1.06 | 0.382 | 0.771 | 1.000 | 21811 | tags=45%, list=40%, signal=74% | |
2160 | TRIGLYCERIDE BIOSYNTHETIC PROCESS | 126 | -0.29 | -1.06 | 0.394 | 0.771 | 1.000 | 24351 | tags=55%, list=45%, signal=99% | |
2161 | REGULATION OF T CELL MEDIATED IMMUNITY | 105 | -0.29 | -1.06 | 0.352 | 0.771 | 1.000 | 17597 | tags=39%, list=32%, signal=57% | |
2162 | FC-EPSILON RECEPTOR SIGNALING PATHWAY | 851 | -0.25 | -1.06 | 0.361 | 0.771 | 1.000 | 26927 | tags=54%, list=49%, signal=105% | |
2163 | REGULATION OF MITOCHONDRIAL MEMBRANE POTENTIAL | 81 | -0.28 | -1.06 | 0.409 | 0.770 | 1.000 | 25775 | tags=57%, list=47%, signal=107% | |
2164 | CELLULAR RESPONSE TO NUTRIENT | 34 | -0.33 | -1.06 | 0.395 | 0.772 | 1.000 | 15550 | tags=44%, list=28%, signal=62% | |
2165 | ACYL-COA METABOLIC PROCESS | 130 | -0.28 | -1.06 | 0.411 | 0.771 | 1.000 | 24487 | tags=55%, list=45%, signal=100% | |
2166 | THIOESTER METABOLIC PROCESS | 130 | -0.28 | -1.06 | 0.411 | 0.771 | 1.000 | 24487 | tags=55%, list=45%, signal=100% | |
2167 | DNA REPLICATION, SYNTHESIS OF RNA PRIMER | 4 | -0.57 | -1.06 | 0.409 | 0.771 | 1.000 | 11412 | tags=50%, list=21%, signal=63% | |
2168 | MONOUBIQUITINATED PROTEIN DEUBIQUITINATION | 32 | -0.38 | -1.06 | 0.426 | 0.770 | 1.000 | 15185 | tags=50%, list=28%, signal=69% | |
2169 | REGULATION OF TOLL-LIKE RECEPTOR SIGNALING PATHWAY | 73 | -0.30 | -1.06 | 0.373 | 0.771 | 1.000 | 32672 | tags=70%, list=60%, signal=173% | |
2170 | CAMP BIOSYNTHETIC PROCESS | 42 | -0.32 | -1.06 | 0.398 | 0.771 | 1.000 | 11449 | tags=29%, list=21%, signal=36% | |
2171 | REGULATION OF MICROTUBULE POLYMERIZATION OR DEPOLYMERIZATION | 99 | -0.28 | -1.06 | 0.398 | 0.771 | 1.000 | 18901 | tags=44%, list=35%, signal=68% | |
2172 | RNA DESTABILIZATION | 20 | -0.38 | -1.06 | 0.435 | 0.771 | 1.000 | 23643 | tags=70%, list=43%, signal=123% | |
2173 | MRNA DESTABILIZATION | 20 | -0.38 | -1.06 | 0.435 | 0.770 | 1.000 | 23643 | tags=70%, list=43%, signal=123% | |
2174 | CHOLESTEROL METABOLIC PROCESS | 113 | -0.28 | -1.06 | 0.395 | 0.771 | 1.000 | 26011 | tags=57%, list=48%, signal=108% | |
2175 | POSITIVE REGULATION OF MYELOID LEUKOCYTE MEDIATED IMMUNITY | 12 | -0.42 | -1.06 | 0.398 | 0.770 | 1.000 | 14887 | tags=50%, list=27%, signal=69% | |
2176 | POSITIVE REGULATION OF CYTOSKELETON ORGANIZATION | 290 | -0.26 | -1.06 | 0.403 | 0.771 | 1.000 | 30177 | tags=62%, list=55%, signal=139% | |
2177 | NEGATIVE REGULATION OF TRANSMEMBRANE TRANSPORT | 140 | -0.26 | -1.06 | 0.384 | 0.771 | 1.000 | 26192 | tags=54%, list=48%, signal=103% | |
2178 | NEGATIVE REGULATION OF DEPHOSPHORYLATION | 179 | -0.28 | -1.06 | 0.363 | 0.771 | 1.000 | 22627 | tags=51%, list=41%, signal=86% | |
2179 | CELLULAR RESPONSE TO MONOSACCHARIDE STIMULUS | 44 | -0.32 | -1.06 | 0.423 | 0.771 | 1.000 | 22892 | tags=61%, list=42%, signal=105% | |
2180 | CELLULAR RESPONSE TO HEXOSE STIMULUS | 44 | -0.32 | -1.06 | 0.423 | 0.771 | 1.000 | 22892 | tags=61%, list=42%, signal=105% | |
2181 | SMAD PROTEIN COMPLEX ASSEMBLY | 27 | -0.36 | -1.06 | 0.412 | 0.770 | 1.000 | 19004 | tags=56%, list=35%, signal=85% | |
2182 | RESPONSE TO UV-C | 21 | -0.38 | -1.06 | 0.403 | 0.770 | 1.000 | 24559 | tags=71%, list=45%, signal=130% | |
2183 | REGULATION OF NITRIC-OXIDE SYNTHASE ACTIVITY | 113 | -0.27 | -1.06 | 0.355 | 0.770 | 1.000 | 12819 | tags=29%, list=23%, signal=38% | |
2184 | RESPONSE TO REACTIVE OXYGEN SPECIES | 196 | -0.28 | -1.06 | 0.413 | 0.770 | 1.000 | 15390 | tags=37%, list=28%, signal=51% | |
2185 | FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 776 | -0.24 | -1.06 | 0.377 | 0.770 | 1.000 | 26927 | tags=54%, list=49%, signal=104% | |
2186 | ATTACHMENT OF SPINDLE MICROTUBULES TO KINETOCHORE | 33 | -0.33 | -1.06 | 0.405 | 0.770 | 1.000 | 24017 | tags=61%, list=44%, signal=108% | |
2187 | CHROMATIN SILENCING AT RDNA | 51 | -0.31 | -1.06 | 0.413 | 0.770 | 1.000 | 28239 | tags=65%, list=52%, signal=134% | |
2188 | PRESYNAPTIC PROCESS INVOLVED IN SYNAPTIC TRANSMISSION | 38 | -0.31 | -1.06 | 0.409 | 0.771 | 1.000 | 14809 | tags=37%, list=27%, signal=50% | |
2189 | ORGANIC HYDROXY COMPOUND METABOLIC PROCESS | 683 | -0.25 | -1.06 | 0.361 | 0.771 | 1.000 | 21842 | tags=47%, list=40%, signal=77% | |
2190 | EXOCYTOSIS | 401 | -0.27 | -1.06 | 0.409 | 0.771 | 1.000 | 16510 | tags=38%, list=30%, signal=54% | |
2191 | ALCOHOL CATABOLIC PROCESS | 50 | -0.32 | -1.06 | 0.430 | 0.771 | 1.000 | 18704 | tags=52%, list=34%, signal=79% | |
2192 | NUCLEOTIDE-BINDING OLIGOMERIZATION DOMAIN CONTAINING SIGNALING PATHWAY | 67 | -0.34 | -1.06 | 0.451 | 0.771 | 1.000 | 25045 | tags=66%, list=46%, signal=121% | |
2193 | CELLULAR RESPONSE TO HORMONE STIMULUS | 1240 | -0.24 | -1.06 | 0.391 | 0.771 | 1.000 | 25186 | tags=50%, list=46%, signal=90% | |
2194 | CELLULAR RESPONSE TO MECHANICAL STIMULUS | 108 | -0.30 | -1.06 | 0.425 | 0.771 | 1.000 | 18538 | tags=47%, list=34%, signal=71% | |
2195 | CARDIAC ATRIUM DEVELOPMENT | 47 | -0.29 | -1.06 | 0.386 | 0.771 | 1.000 | 12728 | tags=32%, list=23%, signal=42% | |
2196 | NEGATIVE REGULATION OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 52 | -0.32 | -1.06 | 0.400 | 0.771 | 1.000 | 23748 | tags=58%, list=43%, signal=102% | |
2197 | NEGATIVE REGULATION OF PROTEIN LOCALIZATION TO CELL PERIPHERY | 52 | -0.32 | -1.06 | 0.400 | 0.770 | 1.000 | 23748 | tags=58%, list=43%, signal=102% | |
2198 | CELL GROWTH | 156 | -0.28 | -1.06 | 0.368 | 0.771 | 1.000 | 16029 | tags=40%, list=29%, signal=56% | |
2199 | DNA RECOMBINATION | 398 | -0.29 | -1.06 | 0.348 | 0.771 | 1.000 | 24731 | tags=56%, list=45%, signal=102% | |
2200 | CARDIAC ENDOTHELIAL CELL DIFFERENTIATION | 12 | -0.42 | -1.06 | 0.418 | 0.772 | 1.000 | 11222 | tags=33%, list=21%, signal=42% | |
2201 | ENDOCARDIAL CELL DIFFERENTIATION | 12 | -0.42 | -1.06 | 0.418 | 0.772 | 1.000 | 11222 | tags=33%, list=21%, signal=42% | |
2202 | REGULATION OF MRNA PROCESSING | 210 | -0.30 | -1.06 | 0.435 | 0.773 | 1.000 | 21191 | tags=51%, list=39%, signal=83% | |
2203 | FC RECEPTOR MEDIATED STIMULATORY SIGNALING PATHWAY | 285 | -0.27 | -1.06 | 0.395 | 0.773 | 1.000 | 23149 | tags=47%, list=42%, signal=81% | |
2204 | RIBONUCLEOPROTEIN COMPLEX LOCALIZATION | 186 | -0.31 | -1.06 | 0.461 | 0.774 | 1.000 | 22894 | tags=55%, list=42%, signal=95% | |
2205 | RESPONSE TO STEROL DEPLETION | 12 | -0.43 | -1.06 | 0.447 | 0.774 | 1.000 | 18937 | tags=67%, list=35%, signal=102% | |
2206 | SREBP SIGNALING PATHWAY | 12 | -0.43 | -1.06 | 0.447 | 0.774 | 1.000 | 18937 | tags=67%, list=35%, signal=102% | |
2207 | CELLULAR RESPONSE TO STEROL DEPLETION | 12 | -0.43 | -1.06 | 0.447 | 0.773 | 1.000 | 18937 | tags=67%, list=35%, signal=102% | |
2208 | DNA PACKAGING | 221 | -0.26 | -1.06 | 0.382 | 0.773 | 1.000 | 19966 | tags=43%, list=37%, signal=67% | |
2209 | NEGATIVE REGULATION OF RESPONSE TO BIOTIC STIMULUS | 51 | -0.31 | -1.06 | 0.418 | 0.773 | 1.000 | 21267 | tags=51%, list=39%, signal=83% | |
2210 | REGULATION OF CHOLESTEROL METABOLIC PROCESS | 22 | -0.36 | -1.06 | 0.422 | 0.773 | 1.000 | 17857 | tags=50%, list=33%, signal=74% | |
2211 | NEGATIVE REGULATION OF STRESS-ACTIVATED MAPK CASCADE | 89 | -0.31 | -1.06 | 0.408 | 0.773 | 1.000 | 21267 | tags=51%, list=39%, signal=83% | |
2212 | NEGATIVE REGULATION OF STRESS-ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 89 | -0.31 | -1.06 | 0.408 | 0.773 | 1.000 | 21267 | tags=51%, list=39%, signal=83% | |
2213 | HISTONE DEACETYLATION | 73 | -0.28 | -1.06 | 0.418 | 0.773 | 1.000 | 28257 | tags=63%, list=52%, signal=130% | |
2214 | MATERNAL PLACENTA DEVELOPMENT | 19 | -0.36 | -1.06 | 0.425 | 0.773 | 1.000 | 15325 | tags=42%, list=28%, signal=58% | |
2215 | REGULATION OF ARP2/3 COMPLEX-MEDIATED ACTIN NUCLEATION | 19 | -0.38 | -1.05 | 0.426 | 0.773 | 1.000 | 22819 | tags=68%, list=42%, signal=117% | |
2216 | NEGATIVE REGULATION OF LIPOPOLYSACCHARIDE-MEDIATED SIGNALING PATHWAY | 16 | -0.37 | -1.05 | 0.409 | 0.773 | 1.000 | 6573 | tags=25%, list=12%, signal=28% | |
2217 | POSITIVE REGULATION OF APOPTOTIC PROCESS | 1067 | -0.26 | -1.05 | 0.454 | 0.773 | 1.000 | 27645 | tags=59%, list=51%, signal=117% | |
2218 | NEUROTRANSMITTER METABOLIC PROCESS | 31 | -0.29 | -1.05 | 0.403 | 0.773 | 1.000 | 9583 | tags=29%, list=18%, signal=35% | |
2219 | OLIGOSACCHARIDE BIOSYNTHETIC PROCESS | 19 | -0.37 | -1.05 | 0.419 | 0.773 | 1.000 | 21734 | tags=58%, list=40%, signal=96% | |
2220 | ENTRAINMENT OF CIRCADIAN CLOCK BY PHOTOPERIOD | 48 | -0.29 | -1.05 | 0.397 | 0.773 | 1.000 | 22427 | tags=52%, list=41%, signal=88% | |
2221 | MITOCHONDRION LOCALIZATION | 46 | -0.31 | -1.05 | 0.423 | 0.773 | 1.000 | 26112 | tags=63%, list=48%, signal=121% | |
2222 | GLUTAMINE METABOLIC PROCESS | 21 | -0.37 | -1.05 | 0.418 | 0.773 | 1.000 | 16384 | tags=52%, list=30%, signal=75% | |
2223 | POSITIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE/THREONINE KINASE SIGNALING PATHWAY | 162 | -0.26 | -1.05 | 0.389 | 0.773 | 1.000 | 12304 | tags=30%, list=23%, signal=38% | |
2224 | COENZYME CATABOLIC PROCESS | 14 | -0.40 | -1.05 | 0.406 | 0.773 | 1.000 | 16565 | tags=57%, list=30%, signal=82% | |
2225 | ORGANIC HYDROXY COMPOUND CATABOLIC PROCESS | 68 | -0.30 | -1.05 | 0.430 | 0.773 | 1.000 | 20089 | tags=51%, list=37%, signal=81% | |
2226 | REGULATION OF THYMOCYTE APOPTOTIC PROCESS | 13 | -0.39 | -1.05 | 0.395 | 0.774 | 1.000 | 20018 | tags=54%, list=37%, signal=85% | |
2227 | NEGATIVE REGULATION OF TRANSCRIPTION REGULATORY REGION DNA BINDING | 22 | -0.33 | -1.05 | 0.388 | 0.774 | 1.000 | 27250 | tags=59%, list=50%, signal=118% | |
2228 | MAINTENANCE OF LOCATION | 210 | -0.27 | -1.05 | 0.416 | 0.774 | 1.000 | 21969 | tags=48%, list=40%, signal=79% | |
2229 | NEGATIVE REGULATION OF RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 37 | -0.30 | -1.05 | 0.398 | 0.774 | 1.000 | 5785 | tags=24%, list=11%, signal=27% | |
2230 | SOMATIC RECOMBINATION OF IMMUNOGLOBULIN GENE SEGMENTS | 39 | -0.30 | -1.05 | 0.403 | 0.774 | 1.000 | 18286 | tags=44%, list=33%, signal=65% | |
2231 | CELLULAR COMPONENT MAINTENANCE | 19 | -0.37 | -1.05 | 0.408 | 0.774 | 1.000 | 22748 | tags=63%, list=42%, signal=108% | |
2232 | POSITIVE REGULATION OF PROGRAMMED CELL DEATH | 1073 | -0.26 | -1.05 | 0.452 | 0.774 | 1.000 | 27645 | tags=59%, list=51%, signal=117% | |
2233 | POSITIVE REGULATION OF INSULIN SECRETION | 65 | -0.30 | -1.05 | 0.426 | 0.775 | 1.000 | 23125 | tags=57%, list=42%, signal=99% | |
2234 | MAMMARY GLAND EPITHELIAL CELL DIFFERENTIATION | 19 | -0.35 | -1.05 | 0.392 | 0.774 | 1.000 | 25311 | tags=58%, list=46%, signal=108% | |
2235 | REGULATION OF CELL CYCLE G2/M PHASE TRANSITION | 104 | -0.29 | -1.05 | 0.422 | 0.775 | 1.000 | 15452 | tags=38%, list=28%, signal=54% | |
2236 | EMBRYONIC PLACENTA DEVELOPMENT | 43 | -0.29 | -1.05 | 0.411 | 0.774 | 1.000 | 25051 | tags=58%, list=46%, signal=107% | |
2237 | REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 355 | -0.26 | -1.05 | 0.388 | 0.774 | 1.000 | 29141 | tags=60%, list=53%, signal=127% | |
2238 | MICROTUBULE POLYMERIZATION OR DEPOLYMERIZATION | 76 | -0.31 | -1.05 | 0.439 | 0.775 | 1.000 | 26595 | tags=66%, list=49%, signal=128% | |
2239 | RESPONSE TO CHOLESTEROL | 35 | -0.30 | -1.05 | 0.411 | 0.775 | 1.000 | 19257 | tags=46%, list=35%, signal=71% | |
2240 | POSITIVE REGULATION OF SECRETION | 449 | -0.25 | -1.05 | 0.424 | 0.775 | 1.000 | 23143 | tags=47%, list=42%, signal=81% | |
2241 | NEGATIVE REGULATION OF INNATE IMMUNE RESPONSE | 67 | -0.33 | -1.05 | 0.445 | 0.776 | 1.000 | 14348 | tags=42%, list=26%, signal=57% | |
2242 | GLUTAMINE FAMILY AMINO ACID BIOSYNTHETIC PROCESS | 22 | -0.38 | -1.05 | 0.442 | 0.777 | 1.000 | 31362 | tags=86%, list=57%, signal=202% | |
2243 | REGULATION OF OXIDATIVE PHOSPHORYLATION | 17 | -0.39 | -1.05 | 0.426 | 0.777 | 1.000 | 14129 | tags=47%, list=26%, signal=63% | |
2244 | POSITIVE REGULATION OF PROTEIN IMPORT INTO NUCLEUS | 174 | -0.28 | -1.05 | 0.423 | 0.777 | 1.000 | 29089 | tags=62%, list=53%, signal=132% | |
2245 | ATP TRANSPORT | 9 | -0.42 | -1.05 | 0.403 | 0.777 | 1.000 | 9403 | tags=33%, list=17%, signal=40% | |
2246 | REGULATION OF SMAD PROTEIN IMPORT INTO NUCLEUS | 43 | -0.31 | -1.05 | 0.404 | 0.777 | 1.000 | 30547 | tags=70%, list=56%, signal=158% | |
2247 | SKELETAL MUSCLE TISSUE DEVELOPMENT | 74 | -0.27 | -1.05 | 0.398 | 0.777 | 1.000 | 16851 | tags=39%, list=31%, signal=57% | |
2248 | POSITIVE REGULATION OF REPRODUCTIVE PROCESS | 42 | -0.31 | -1.05 | 0.410 | 0.778 | 1.000 | 22260 | tags=52%, list=41%, signal=88% | |
2249 | POSITIVE REGULATION OF GRANULOCYTE DIFFERENTIATION | 31 | -0.31 | -1.05 | 0.381 | 0.777 | 1.000 | 27116 | tags=52%, list=50%, signal=102% | |
2250 | CARDIAC ATRIUM MORPHOGENESIS | 36 | -0.31 | -1.05 | 0.407 | 0.778 | 1.000 | 12728 | tags=33%, list=23%, signal=43% | |
2251 | NEGATIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 803 | -0.26 | -1.05 | 0.443 | 0.778 | 1.000 | 22937 | tags=48%, list=42%, signal=82% | |
2252 | RESPONSE TO ERYTHROPOIETIN | 10 | -0.45 | -1.05 | 0.413 | 0.778 | 1.000 | 20555 | tags=70%, list=38%, signal=112% | |
2253 | CELLULAR RESPONSE TO ERYTHROPOIETIN | 10 | -0.45 | -1.05 | 0.413 | 0.778 | 1.000 | 20555 | tags=70%, list=38%, signal=112% | |
2254 | POSITIVE REGULATION OF PROTEIN OLIGOMERIZATION | 41 | -0.33 | -1.05 | 0.468 | 0.778 | 1.000 | 18803 | tags=51%, list=34%, signal=78% | |
2255 | POSITIVE REGULATION OF LYMPHOCYTE MEDIATED IMMUNITY | 101 | -0.29 | -1.05 | 0.419 | 0.778 | 1.000 | 17597 | tags=41%, list=32%, signal=60% | |
2256 | REGULATION OF CELLULAR COMPONENT BIOGENESIS | 1231 | -0.26 | -1.05 | 0.391 | 0.778 | 1.000 | 25994 | tags=54%, list=48%, signal=101% | |
2257 | INTRACELLULAR RECEPTOR SIGNALING PATHWAY | 381 | -0.26 | -1.05 | 0.425 | 0.778 | 1.000 | 23466 | tags=50%, list=43%, signal=87% | |
2258 | TOLL-LIKE RECEPTOR TLR1:TLR2 SIGNALING PATHWAY | 197 | -0.29 | -1.05 | 0.450 | 0.778 | 1.000 | 25375 | tags=59%, list=46%, signal=109% | |
2259 | TOLL-LIKE RECEPTOR TLR6:TLR2 SIGNALING PATHWAY | 197 | -0.29 | -1.05 | 0.450 | 0.778 | 1.000 | 25375 | tags=59%, list=46%, signal=109% | |
2260 | FATTY-ACYL-COA METABOLIC PROCESS | 99 | -0.29 | -1.05 | 0.444 | 0.777 | 1.000 | 24487 | tags=56%, list=45%, signal=100% | |
2261 | L-ASPARTATE TRANSPORT | 8 | -0.37 | -1.05 | 0.400 | 0.778 | 1.000 | 6391 | tags=38%, list=12%, signal=42% | |
2262 | L-ASPARTATE TRANSMEMBRANE TRANSPORT | 8 | -0.37 | -1.05 | 0.400 | 0.778 | 1.000 | 6391 | tags=38%, list=12%, signal=42% | |
2263 | DNA STRAND ELONGATION | 77 | -0.30 | -1.05 | 0.434 | 0.777 | 1.000 | 19793 | tags=51%, list=36%, signal=79% | |
2264 | REGULATION OF CELL-CELL ADHESION MEDIATED BY CADHERIN | 15 | -0.39 | -1.05 | 0.426 | 0.777 | 1.000 | 13433 | tags=47%, list=25%, signal=62% | |
2265 | GLIOGENESIS | 157 | -0.27 | -1.05 | 0.423 | 0.777 | 1.000 | 26582 | tags=59%, list=49%, signal=115% | |
2266 | REGULATION OF DEFENSE RESPONSE TO VIRUS | 384 | -0.26 | -1.05 | 0.437 | 0.777 | 1.000 | 21561 | tags=47%, list=39%, signal=78% | |
2267 | POSITIVE REGULATION OF CELLULAR COMPONENT BIOGENESIS | 639 | -0.26 | -1.05 | 0.454 | 0.777 | 1.000 | 29523 | tags=61%, list=54%, signal=130% | |
2268 | NEGATIVE REGULATION OF VIRAL LIFE CYCLE | 196 | -0.28 | -1.05 | 0.427 | 0.777 | 1.000 | 24449 | tags=54%, list=45%, signal=97% | |
2269 | POSITIVE REGULATION OF CYTOPLASMIC TRANSPORT | 521 | -0.26 | -1.05 | 0.379 | 0.777 | 1.000 | 22928 | tags=48%, list=42%, signal=82% | |
2270 | REGULATION OF CAMP-MEDIATED SIGNALING | 52 | -0.30 | -1.05 | 0.406 | 0.777 | 1.000 | 16270 | tags=37%, list=30%, signal=52% | |
2271 | REACTIVE NITROGEN SPECIES METABOLIC PROCESS | 83 | -0.28 | -1.05 | 0.417 | 0.777 | 1.000 | 12646 | tags=33%, list=23%, signal=42% | |
2272 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO CELL SURFACE | 11 | -0.41 | -1.05 | 0.409 | 0.778 | 1.000 | 26312 | tags=73%, list=48%, signal=140% | |
2273 | NEGATIVE REGULATION OF CYTOPLASMIC TRANSPORT | 231 | -0.26 | -1.05 | 0.393 | 0.778 | 1.000 | 23310 | tags=48%, list=43%, signal=84% | |
2274 | CELLULAR GLUCOSE HOMEOSTASIS | 57 | -0.31 | -1.05 | 0.482 | 0.778 | 1.000 | 27317 | tags=68%, list=50%, signal=137% | |
2275 | NEGATIVE REGULATION OF VIRAL PROCESS | 204 | -0.28 | -1.05 | 0.436 | 0.778 | 1.000 | 19204 | tags=44%, list=35%, signal=67% | |
2276 | RHYTHMIC PROCESS | 317 | -0.27 | -1.05 | 0.424 | 0.778 | 1.000 | 22427 | tags=49%, list=41%, signal=82% | |
2277 | REGULATION OF OXIDOREDUCTASE ACTIVITY | 176 | -0.26 | -1.05 | 0.385 | 0.778 | 1.000 | 17005 | tags=36%, list=31%, signal=53% | |
2278 | NEGATIVE REGULATION OF PHOSPHATASE ACTIVITY | 169 | -0.28 | -1.05 | 0.400 | 0.778 | 1.000 | 22627 | tags=50%, list=41%, signal=86% | |
2279 | DNA DEAMINATION | 20 | -0.33 | -1.04 | 0.425 | 0.778 | 1.000 | 29684 | tags=80%, list=54%, signal=175% | |
2280 | BONE RESORPTION | 19 | -0.36 | -1.04 | 0.416 | 0.778 | 1.000 | 22991 | tags=47%, list=42%, signal=82% | |
2281 | CENTRIOLE-CENTRIOLE COHESION | 17 | -0.37 | -1.04 | 0.437 | 0.779 | 1.000 | 16463 | tags=53%, list=30%, signal=76% | |
2282 | T CELL MEDIATED IMMUNITY | 41 | -0.32 | -1.04 | 0.403 | 0.779 | 1.000 | 24502 | tags=61%, list=45%, signal=110% | |
2283 | REGULATION OF PEPTIDYL-SERINE PHOSPHORYLATION | 171 | -0.27 | -1.04 | 0.431 | 0.778 | 1.000 | 21164 | tags=48%, list=39%, signal=78% | |
2284 | ISOPRENOID BIOSYNTHETIC PROCESS | 20 | -0.37 | -1.04 | 0.422 | 0.779 | 1.000 | 13550 | tags=45%, list=25%, signal=60% | |
2285 | CARGO LOADING INTO VESICLE | 23 | -0.38 | -1.04 | 0.438 | 0.778 | 1.000 | 15793 | tags=52%, list=29%, signal=73% | |
2286 | RNA INTERFERENCE | 14 | -0.37 | -1.04 | 0.407 | 0.778 | 1.000 | 32076 | tags=86%, list=59%, signal=207% | |
2287 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 110 | -0.30 | -1.04 | 0.472 | 0.779 | 1.000 | 18530 | tags=45%, list=34%, signal=69% | |
2288 | REGULATION OF PROTEIN COMPLEX DISASSEMBLY | 129 | -0.28 | -1.04 | 0.418 | 0.779 | 1.000 | 19184 | tags=44%, list=35%, signal=68% | |
2289 | REGULATION OF PROTEIN IMPORT | 313 | -0.26 | -1.04 | 0.435 | 0.780 | 1.000 | 29141 | tags=60%, list=53%, signal=127% | |
2290 | POSITIVE REGULATION OF DNA-DEPENDENT DNA REPLICATION | 22 | -0.36 | -1.04 | 0.433 | 0.780 | 1.000 | 2700 | tags=23%, list=5%, signal=24% | |
2291 | NEGATIVE REGULATION OF FAT CELL PROLIFERATION | 12 | -0.40 | -1.04 | 0.430 | 0.780 | 1.000 | 24049 | tags=67%, list=44%, signal=119% | |
2292 | REGULATION OF EXOCYTOSIS | 199 | -0.27 | -1.04 | 0.431 | 0.780 | 1.000 | 24179 | tags=53%, list=44%, signal=94% | |
2293 | REGULATION OF MONOOXYGENASE ACTIVITY | 132 | -0.27 | -1.04 | 0.383 | 0.780 | 1.000 | 11503 | tags=27%, list=21%, signal=34% | |
2294 | NEGATIVE REGULATION OF CHEMOKINE PRODUCTION | 27 | -0.33 | -1.04 | 0.433 | 0.780 | 1.000 | 19583 | tags=52%, list=36%, signal=81% | |
2295 | REGULATION OF MAP KINASE ACTIVITY | 940 | -0.24 | -1.04 | 0.410 | 0.780 | 1.000 | 23284 | tags=46%, list=43%, signal=79% | |
2296 | REGULATION OF DNA REPLICATION | 336 | -0.26 | -1.04 | 0.440 | 0.779 | 1.000 | 23271 | tags=49%, list=43%, signal=84% | |
2297 | BRANCHED-CHAIN AMINO ACID CATABOLIC PROCESS | 58 | -0.30 | -1.04 | 0.433 | 0.779 | 1.000 | 29335 | tags=67%, list=54%, signal=145% | |
2298 | CENTROSOME CYCLE | 76 | -0.29 | -1.04 | 0.428 | 0.779 | 1.000 | 32637 | tags=76%, list=60%, signal=189% | |
2299 | ASPARTATE FAMILY AMINO ACID BIOSYNTHETIC PROCESS | 27 | -0.34 | -1.04 | 0.416 | 0.779 | 1.000 | 27293 | tags=70%, list=50%, signal=140% | |
2300 | DEFENSE RESPONSE TO VIRUS | 129 | -0.30 | -1.04 | 0.449 | 0.779 | 1.000 | 24809 | tags=59%, list=45%, signal=108% | |
2301 | REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE/THREONINE KINASE SIGNALING PATHWAY | 352 | -0.25 | -1.04 | 0.443 | 0.779 | 1.000 | 25501 | tags=52%, list=47%, signal=97% | |
2302 | ERYTHROCYTE DIFFERENTIATION | 79 | -0.29 | -1.04 | 0.441 | 0.779 | 1.000 | 28934 | tags=62%, list=53%, signal=132% | |
2303 | REGULATION OF VIRAL ENTRY INTO HOST CELL | 52 | -0.33 | -1.04 | 0.438 | 0.778 | 1.000 | 21481 | tags=58%, list=39%, signal=95% | |
2304 | POSITIVE REGULATION OF CELL DEATH | 1120 | -0.26 | -1.04 | 0.481 | 0.778 | 1.000 | 27645 | tags=58%, list=51%, signal=116% | |
2305 | REGULATION OF G-PROTEIN COUPLED RECEPTOR PROTEIN SIGNALING PATHWAY | 245 | -0.24 | -1.04 | 0.420 | 0.778 | 1.000 | 20717 | tags=41%, list=38%, signal=66% | |
2306 | MYD88-DEPENDENT TOLL-LIKE RECEPTOR SIGNALING PATHWAY | 211 | -0.29 | -1.04 | 0.466 | 0.778 | 1.000 | 25375 | tags=59%, list=46%, signal=109% | |
2307 | REGULATION OF MEIOTIC CELL CYCLE | 20 | -0.37 | -1.04 | 0.432 | 0.779 | 1.000 | 17225 | tags=50%, list=32%, signal=73% | |
2308 | POSITIVE REGULATION OF ENDOCYTOSIS | 206 | -0.26 | -1.04 | 0.401 | 0.779 | 1.000 | 8297 | tags=24%, list=15%, signal=29% | |
2309 | NEGATIVE REGULATION OF PROTEIN DEPHOSPHORYLATION | 177 | -0.28 | -1.04 | 0.406 | 0.779 | 1.000 | 22627 | tags=50%, list=41%, signal=86% | |
2310 | REGULATION OF LYMPHOCYTE MEDIATED IMMUNITY | 172 | -0.28 | -1.04 | 0.405 | 0.780 | 1.000 | 7829 | tags=24%, list=14%, signal=28% | |
2311 | REGULATION OF PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 123 | -0.30 | -1.04 | 0.470 | 0.782 | 1.000 | 22492 | tags=55%, list=41%, signal=94% | |
2312 | RESPONSE TO FIBROBLAST GROWTH FACTOR | 819 | -0.24 | -1.04 | 0.414 | 0.781 | 1.000 | 22329 | tags=45%, list=41%, signal=74% | |
2313 | POSITIVE REGULATION OF DNA BINDING | 58 | -0.30 | -1.04 | 0.431 | 0.781 | 1.000 | 19596 | tags=45%, list=36%, signal=70% | |
2314 | MODIFIED AMINO ACID TRANSPORT | 45 | -0.30 | -1.04 | 0.423 | 0.781 | 1.000 | 20980 | tags=47%, list=38%, signal=76% | |
2315 | NUCLEOTIDE-BINDING DOMAIN, LEUCINE RICH REPEAT CONTAINING RECEPTOR SIGNALING PATHWAY | 114 | -0.31 | -1.04 | 0.467 | 0.781 | 1.000 | 25172 | tags=61%, list=46%, signal=114% | |
2316 | CELLULAR RESPONSE TO FIBROBLAST GROWTH FACTOR STIMULUS | 815 | -0.24 | -1.04 | 0.415 | 0.781 | 1.000 | 22329 | tags=45%, list=41%, signal=75% | |
2317 | PHOTOTRANSDUCTION, VISIBLE LIGHT | 209 | -0.24 | -1.04 | 0.393 | 0.781 | 1.000 | 19295 | tags=39%, list=35%, signal=60% | |
2318 | REGULATION OF GENERATION OF PRECURSOR METABOLITES AND ENERGY | 141 | -0.27 | -1.04 | 0.427 | 0.781 | 1.000 | 28364 | tags=60%, list=52%, signal=123% | |
2319 | POSITIVE REGULATION OF GTPASE ACTIVITY | 757 | -0.24 | -1.04 | 0.439 | 0.780 | 1.000 | 25975 | tags=51%, list=48%, signal=97% | |
2320 | L-METHIONINE BIOSYNTHETIC PROCESS FROM METHYLTHIOADENOSINE | 14 | -0.40 | -1.04 | 0.406 | 0.780 | 1.000 | 27293 | tags=79%, list=50%, signal=157% | |
2321 | NEGATIVE REGULATION OF INCLUSION BODY ASSEMBLY | 19 | -0.40 | -1.04 | 0.424 | 0.780 | 1.000 | 32700 | tags=100%, list=60%, signal=249% | |
2322 | RESPONSE TO LIPID | 724 | -0.25 | -1.04 | 0.411 | 0.781 | 1.000 | 21390 | tags=43%, list=39%, signal=69% | |
2323 | REGULATION OF HORMONE METABOLIC PROCESS | 50 | -0.31 | -1.04 | 0.437 | 0.781 | 1.000 | 21312 | tags=48%, list=39%, signal=79% | |
2324 | POSITIVE REGULATION OF INTERLEUKIN-1 BETA SECRETION | 27 | -0.35 | -1.04 | 0.446 | 0.781 | 1.000 | 13148 | tags=37%, list=24%, signal=49% | |
2325 | NEGATIVE REGULATION OF MAP KINASE ACTIVITY | 132 | -0.29 | -1.04 | 0.428 | 0.781 | 1.000 | 23870 | tags=52%, list=44%, signal=91% | |
2326 | REGULATION OF ACTIN NUCLEATION | 34 | -0.33 | -1.04 | 0.441 | 0.781 | 1.000 | 19435 | tags=53%, list=36%, signal=82% | |
2327 | REGULATION OF POLYSACCHARIDE BIOSYNTHETIC PROCESS | 75 | -0.27 | -1.04 | 0.414 | 0.781 | 1.000 | 13561 | tags=32%, list=25%, signal=42% | |
2328 | REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY BY P53 CLASS MEDIATOR | 33 | -0.34 | -1.04 | 0.422 | 0.781 | 1.000 | 20622 | tags=58%, list=38%, signal=92% | |
2329 | REGULATION OF MITOTIC NUCLEAR DIVISION | 303 | -0.27 | -1.04 | 0.422 | 0.781 | 1.000 | 26241 | tags=58%, list=48%, signal=110% | |
2330 | CIRCADIAN REGULATION OF GENE EXPRESSION | 160 | -0.28 | -1.04 | 0.439 | 0.781 | 1.000 | 23751 | tags=52%, list=43%, signal=91% | |
2331 | POSITIVE REGULATION OF SMAD PROTEIN IMPORT INTO NUCLEUS | 34 | -0.32 | -1.04 | 0.428 | 0.781 | 1.000 | 29914 | tags=68%, list=55%, signal=149% | |
2332 | SUCCINATE METABOLIC PROCESS | 14 | -0.41 | -1.04 | 0.442 | 0.780 | 1.000 | 23419 | tags=71%, list=43%, signal=125% | |
2333 | INTERACTION WITH HOST | 254 | -0.29 | -1.04 | 0.405 | 0.780 | 1.000 | 25229 | tags=59%, list=46%, signal=110% | |
2334 | NEGATIVE REGULATION OF LYMPHOCYTE MEDIATED IMMUNITY | 60 | -0.34 | -1.04 | 0.453 | 0.780 | 1.000 | 9310 | tags=30%, list=17%, signal=36% | |
2335 | KETONE BODY BIOSYNTHETIC PROCESS | 14 | -0.37 | -1.04 | 0.429 | 0.780 | 1.000 | 19720 | tags=50%, list=36%, signal=78% | |
2336 | SULFUR COMPOUND TRANSPORT | 43 | -0.31 | -1.04 | 0.443 | 0.780 | 1.000 | 27701 | tags=67%, list=51%, signal=137% | |
2337 | POLY(A)+ MRNA EXPORT FROM NUCLEUS | 19 | -0.35 | -1.04 | 0.457 | 0.781 | 1.000 | 22090 | tags=58%, list=40%, signal=97% | |
2338 | HISTONE H3-K9 DEMETHYLATION | 14 | -0.36 | -1.04 | 0.453 | 0.780 | 1.000 | 16729 | tags=50%, list=31%, signal=72% | |
2339 | 3'-UTR-MEDIATED MRNA DESTABILIZATION | 11 | -0.40 | -1.04 | 0.441 | 0.781 | 1.000 | 23643 | tags=73%, list=43%, signal=128% | |
2340 | POTASSIUM ION IMPORT | 23 | -0.34 | -1.04 | 0.446 | 0.781 | 1.000 | 16903 | tags=43%, list=31%, signal=63% | |
2341 | SYNAPTIC VESICLE RECYCLING | 35 | -0.31 | -1.04 | 0.397 | 0.781 | 1.000 | 16426 | tags=40%, list=30%, signal=57% | |
2342 | POSITIVE REGULATION OF CELL-SUBSTRATE ADHESION | 153 | -0.26 | -1.04 | 0.444 | 0.782 | 1.000 | 22054 | tags=46%, list=40%, signal=78% | |
2343 | INTERFERON-GAMMA SECRETION | 12 | -0.41 | -1.04 | 0.435 | 0.782 | 1.000 | 28163 | tags=83%, list=52%, signal=172% | |
2344 | POSITIVE REGULATION BY HOST OF VIRAL PROCESS | 29 | -0.33 | -1.04 | 0.450 | 0.782 | 1.000 | 20245 | tags=55%, list=37%, signal=88% | |
2345 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER INVOLVED IN CELLULAR RESPONSE TO CHEMICAL STIMULUS | 62 | -0.30 | -1.04 | 0.450 | 0.781 | 1.000 | 22985 | tags=53%, list=42%, signal=92% | |
2346 | REGULATION OF CYTOKINESIS | 194 | -0.26 | -1.04 | 0.417 | 0.781 | 1.000 | 19751 | tags=42%, list=36%, signal=66% | |
2347 | ASYMMETRIC PROTEIN LOCALIZATION | 9 | -0.40 | -1.04 | 0.413 | 0.781 | 1.000 | 12051 | tags=44%, list=22%, signal=57% | |
2348 | RIBONUCLEOPROTEIN COMPLEX EXPORT FROM NUCLEUS | 182 | -0.30 | -1.04 | 0.477 | 0.781 | 1.000 | 22894 | tags=55%, list=42%, signal=94% | |
2349 | RRNA CATABOLIC PROCESS | 14 | -0.41 | -1.04 | 0.464 | 0.781 | 1.000 | 29604 | tags=93%, list=54%, signal=202% | |
2350 | DICARBOXYLIC ACID CATABOLIC PROCESS | 27 | -0.33 | -1.04 | 0.445 | 0.781 | 1.000 | 23419 | tags=59%, list=43%, signal=104% | |
2351 | RAP PROTEIN SIGNAL TRANSDUCTION | 30 | -0.32 | -1.03 | 0.395 | 0.781 | 1.000 | 16795 | tags=43%, list=31%, signal=63% | |
2352 | REGULATION OF VIRAL GENOME REPLICATION | 166 | -0.28 | -1.03 | 0.453 | 0.782 | 1.000 | 20245 | tags=46%, list=37%, signal=72% | |
2353 | CELL JUNCTION ORGANIZATION | 419 | -0.25 | -1.03 | 0.432 | 0.782 | 1.000 | 25849 | tags=53%, list=47%, signal=99% | |
2354 | CELLULAR KETONE METABOLIC PROCESS | 83 | -0.30 | -1.03 | 0.444 | 0.782 | 1.000 | 28279 | tags=66%, list=52%, signal=137% | |
2355 | ALPHA-AMINO ACID CATABOLIC PROCESS | 166 | -0.26 | -1.03 | 0.441 | 0.782 | 1.000 | 25109 | tags=51%, list=46%, signal=94% | |
2356 | PROTEIN-DNA COMPLEX SUBUNIT ORGANIZATION | 229 | -0.28 | -1.03 | 0.423 | 0.782 | 1.000 | 19992 | tags=46%, list=37%, signal=73% | |
2357 | CELLULAR RESPONSE TO ORGANONITROGEN COMPOUND | 1243 | -0.23 | -1.03 | 0.464 | 0.783 | 1.000 | 25186 | tags=49%, list=46%, signal=89% | |
2358 | REGULATION OF ALTERNATIVE MRNA SPLICING, VIA SPLICEOSOME | 79 | -0.29 | -1.03 | 0.428 | 0.783 | 1.000 | 21095 | tags=48%, list=39%, signal=78% | |
2359 | RESPONSE TO TRANSFORMING GROWTH FACTOR BETA | 356 | -0.27 | -1.03 | 0.407 | 0.783 | 1.000 | 20835 | tags=46%, list=38%, signal=74% | |
2360 | RESPONSE TO LIGHT STIMULUS | 561 | -0.24 | -1.03 | 0.415 | 0.783 | 1.000 | 27063 | tags=54%, list=49%, signal=106% | |
2361 | REGULATION OF ADAPTIVE IMMUNE RESPONSE | 179 | -0.28 | -1.03 | 0.423 | 0.783 | 1.000 | 11234 | tags=30%, list=21%, signal=37% | |
2362 | POSITIVE REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 21 | -0.34 | -1.03 | 0.439 | 0.784 | 1.000 | 9527 | tags=33%, list=17%, signal=40% | |
2363 | ACTIVATION OF MAPKK ACTIVITY | 561 | -0.23 | -1.03 | 0.448 | 0.784 | 1.000 | 26855 | tags=53%, list=49%, signal=102% | |
2364 | POSITIVE REGULATION OF INTERLEUKIN-1 PRODUCTION | 46 | -0.33 | -1.03 | 0.439 | 0.784 | 1.000 | 13148 | tags=35%, list=24%, signal=46% | |
2365 | IMMUNE EFFECTOR PROCESS | 677 | -0.26 | -1.03 | 0.429 | 0.785 | 1.000 | 23254 | tags=48%, list=43%, signal=83% | |
2366 | CENTROSOME DUPLICATION | 57 | -0.29 | -1.03 | 0.443 | 0.785 | 1.000 | 32637 | tags=75%, list=60%, signal=187% | |
2367 | POSITIVE REGULATION OF STEM CELL DIFFERENTIATION | 117 | -0.27 | -1.03 | 0.443 | 0.785 | 1.000 | 16858 | tags=37%, list=31%, signal=53% | |
2368 | DNA DEMETHYLATION | 24 | -0.35 | -1.03 | 0.444 | 0.785 | 1.000 | 16813 | tags=46%, list=31%, signal=66% | |
2369 | SEGMENT SPECIFICATION | 12 | -0.39 | -1.03 | 0.463 | 0.785 | 1.000 | 15207 | tags=50%, list=28%, signal=69% | |
2370 | RESPONSE TO ORGANIC CYCLIC COMPOUND | 714 | -0.24 | -1.03 | 0.443 | 0.784 | 1.000 | 17226 | tags=35%, list=32%, signal=50% | |
2371 | REGULATION OF EXTRACELLULAR MATRIX ASSEMBLY | 28 | -0.31 | -1.03 | 0.391 | 0.784 | 1.000 | 18901 | tags=46%, list=35%, signal=71% | |
2372 | GLYCOSIDE CATABOLIC PROCESS | 9 | -0.42 | -1.03 | 0.441 | 0.785 | 1.000 | 14540 | tags=56%, list=27%, signal=76% | |
2373 | MIDBRAIN DEVELOPMENT | 146 | -0.28 | -1.03 | 0.469 | 0.784 | 1.000 | 22521 | tags=52%, list=41%, signal=88% | |
2374 | POSITIVE REGULATION OF ALPHA-BETA T CELL PROLIFERATION | 20 | -0.41 | -1.03 | 0.436 | 0.784 | 1.000 | 25520 | tags=75%, list=47%, signal=141% | |
2375 | PANTOTHENATE METABOLIC PROCESS | 24 | -0.35 | -1.03 | 0.483 | 0.785 | 1.000 | 19336 | tags=54%, list=35%, signal=84% | |
2376 | POSITIVE REGULATION OF INTERLEUKIN-8 SECRETION | 19 | -0.37 | -1.03 | 0.448 | 0.785 | 1.000 | 15663 | tags=47%, list=29%, signal=66% | |
2377 | CELL PROLIFERATION | 940 | -0.24 | -1.03 | 0.440 | 0.785 | 1.000 | 23278 | tags=46%, list=43%, signal=79% | |
2378 | REGULATION OF GLYCOGEN BIOSYNTHETIC PROCESS | 60 | -0.27 | -1.03 | 0.403 | 0.785 | 1.000 | 12145 | tags=30%, list=22%, signal=39% | |
2379 | REGULATION OF GLUCAN BIOSYNTHETIC PROCESS | 60 | -0.27 | -1.03 | 0.403 | 0.785 | 1.000 | 12145 | tags=30%, list=22%, signal=39% | |
2380 | POSITIVE REGULATION OF CATION CHANNEL ACTIVITY | 69 | -0.25 | -1.03 | 0.412 | 0.786 | 1.000 | 20627 | tags=43%, list=38%, signal=70% | |
2381 | ORGANIC HYDROXY COMPOUND BIOSYNTHETIC PROCESS | 238 | -0.25 | -1.03 | 0.443 | 0.786 | 1.000 | 22797 | tags=47%, list=42%, signal=80% | |
2382 | PATTERN RECOGNITION RECEPTOR SIGNALING PATHWAY | 351 | -0.28 | -1.03 | 0.520 | 0.786 | 1.000 | 23696 | tags=53%, list=43%, signal=93% | |
2383 | REGULATION OF CYTOPLASMIC TRANSPORT | 877 | -0.25 | -1.03 | 0.402 | 0.786 | 1.000 | 23015 | tags=47%, list=42%, signal=80% | |
2384 | REGULATION OF SYNAPSE STRUCTURE OR ACTIVITY | 206 | -0.24 | -1.03 | 0.438 | 0.785 | 1.000 | 18655 | tags=38%, list=34%, signal=58% | |
2385 | MEMBRANE PROTEIN ECTODOMAIN PROTEOLYSIS | 51 | -0.32 | -1.03 | 0.495 | 0.786 | 1.000 | 25629 | tags=65%, list=47%, signal=122% | |
2386 | CELL JUNCTION ASSEMBLY | 389 | -0.25 | -1.03 | 0.447 | 0.785 | 1.000 | 25849 | tags=52%, list=47%, signal=98% | |
2387 | REGULATION OF B CELL APOPTOTIC PROCESS | 26 | -0.35 | -1.03 | 0.441 | 0.785 | 1.000 | 21048 | tags=58%, list=38%, signal=94% | |
2388 | REGULATION OF PROTEIN DEACETYLATION | 69 | -0.29 | -1.03 | 0.486 | 0.785 | 1.000 | 25077 | tags=58%, list=46%, signal=107% | |
2389 | NUCLEAR DNA REPLICATION | 46 | -0.32 | -1.03 | 0.470 | 0.785 | 1.000 | 22812 | tags=59%, list=42%, signal=101% | |
2390 | CELL CYCLE DNA REPLICATION | 46 | -0.32 | -1.03 | 0.470 | 0.785 | 1.000 | 22812 | tags=59%, list=42%, signal=101% | |
2391 | DENDRITE DEVELOPMENT | 103 | -0.27 | -1.03 | 0.433 | 0.785 | 1.000 | 29107 | tags=64%, list=53%, signal=137% | |
2392 | REGULATION OF NUCLEAR DIVISION | 316 | -0.27 | -1.03 | 0.438 | 0.785 | 1.000 | 26241 | tags=58%, list=48%, signal=110% | |
2393 | NUCLEIC ACID TRANSPORT | 197 | -0.30 | -1.03 | 0.476 | 0.784 | 1.000 | 23917 | tags=56%, list=44%, signal=100% | |
2394 | RNA TRANSPORT | 197 | -0.30 | -1.03 | 0.476 | 0.784 | 1.000 | 23917 | tags=56%, list=44%, signal=100% | |
2395 | REGULATION OF LIPOPOLYSACCHARIDE-MEDIATED SIGNALING PATHWAY | 34 | -0.32 | -1.03 | 0.435 | 0.784 | 1.000 | 8001 | tags=26%, list=15%, signal=31% | |
2396 | RESPONSE TO INTERFERON-ALPHA | 35 | -0.35 | -1.03 | 0.446 | 0.784 | 1.000 | 27317 | tags=71%, list=50%, signal=143% | |
2397 | POLYOL BIOSYNTHETIC PROCESS | 24 | -0.33 | -1.03 | 0.438 | 0.784 | 1.000 | 11350 | tags=33%, list=21%, signal=42% | |
2398 | DEVELOPMENTAL CELL GROWTH | 94 | -0.28 | -1.03 | 0.485 | 0.785 | 1.000 | 16029 | tags=39%, list=29%, signal=56% | |
2399 | RECEPTOR INTERNALIZATION | 102 | -0.29 | -1.03 | 0.415 | 0.785 | 1.000 | 22297 | tags=49%, list=41%, signal=83% | |
2400 | POSITIVE REGULATION OF CELL PROJECTION ORGANIZATION | 446 | -0.24 | -1.03 | 0.447 | 0.784 | 1.000 | 29312 | tags=58%, list=54%, signal=124% | |
2401 | GLYCOLIPID METABOLIC PROCESS | 199 | -0.27 | -1.03 | 0.415 | 0.784 | 1.000 | 22549 | tags=52%, list=41%, signal=89% | |
2402 | NEGATIVE REGULATION OF SKELETAL MUSCLE TISSUE DEVELOPMENT | 9 | -0.41 | -1.03 | 0.439 | 0.785 | 1.000 | 9877 | tags=33%, list=18%, signal=41% | |
2403 | REGULATION OF TRANSLATIONAL INITIATION | 143 | -0.31 | -1.03 | 0.473 | 0.784 | 1.000 | 30846 | tags=76%, list=56%, signal=173% | |
2404 | TOLL-LIKE RECEPTOR 2 SIGNALING PATHWAY | 199 | -0.29 | -1.03 | 0.483 | 0.784 | 1.000 | 25375 | tags=58%, list=46%, signal=108% | |
2405 | POSITIVE REGULATION OF FIBROBLAST MIGRATION | 27 | -0.31 | -1.03 | 0.423 | 0.784 | 1.000 | 8811 | tags=26%, list=16%, signal=31% | |
2406 | REGULATION OF G2/M TRANSITION OF MITOTIC CELL CYCLE | 91 | -0.29 | -1.03 | 0.458 | 0.785 | 1.000 | 24761 | tags=54%, list=45%, signal=98% | |
2407 | MEGAKARYOCYTE DIFFERENTIATION | 16 | -0.35 | -1.03 | 0.407 | 0.785 | 1.000 | 21845 | tags=44%, list=40%, signal=73% | |
2408 | SMOOTH MUSCLE CELL MIGRATION | 22 | -0.37 | -1.03 | 0.465 | 0.786 | 1.000 | 21303 | tags=59%, list=39%, signal=97% | |
2409 | PROTEIN LOCALIZATION TO CYTOSKELETON | 52 | -0.33 | -1.03 | 0.484 | 0.785 | 1.000 | 29005 | tags=73%, list=53%, signal=155% | |
2410 | POSITIVE REGULATION OF NEURON DEATH | 77 | -0.31 | -1.03 | 0.486 | 0.785 | 1.000 | 27514 | tags=66%, list=50%, signal=133% | |
2411 | ESTABLISHMENT OF LOCALIZATION BY MOVEMENT ALONG MICROTUBULE | 161 | -0.29 | -1.03 | 0.456 | 0.785 | 1.000 | 27400 | tags=65%, list=50%, signal=129% | |
2412 | CELLULAR ALDEHYDE METABOLIC PROCESS | 136 | -0.28 | -1.03 | 0.476 | 0.785 | 1.000 | 24074 | tags=56%, list=44%, signal=100% | |
2413 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO STRESS | 54 | -0.31 | -1.03 | 0.435 | 0.785 | 1.000 | 22985 | tags=52%, list=42%, signal=89% | |
2414 | POSITIVE REGULATION OF MITOTIC METAPHASE/ANAPHASE TRANSITION | 19 | -0.39 | -1.03 | 0.431 | 0.785 | 1.000 | 20376 | tags=63%, list=37%, signal=101% | |
2415 | POSITIVE REGULATION OF MITOTIC SISTER CHROMATID SEPARATION | 19 | -0.39 | -1.03 | 0.431 | 0.785 | 1.000 | 20376 | tags=63%, list=37%, signal=101% | |
2416 | POSITIVE REGULATION OF METAPHASE/ANAPHASE TRANSITION OF CELL CYCLE | 19 | -0.39 | -1.03 | 0.431 | 0.784 | 1.000 | 20376 | tags=63%, list=37%, signal=101% | |
2417 | TOOTH MINERALIZATION | 17 | -0.36 | -1.03 | 0.438 | 0.784 | 1.000 | 13861 | tags=41%, list=25%, signal=55% | |
2418 | THYROID HORMONE GENERATION | 18 | -0.35 | -1.03 | 0.437 | 0.784 | 1.000 | 14270 | tags=39%, list=26%, signal=53% | |
2419 | MRNA TRANSPORT | 173 | -0.30 | -1.03 | 0.487 | 0.784 | 1.000 | 22894 | tags=54%, list=42%, signal=92% | |
2420 | SODIUM ION EXPORT | 26 | -0.34 | -1.03 | 0.431 | 0.784 | 1.000 | 22870 | tags=50%, list=42%, signal=86% | |
2421 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 51 | -0.34 | -1.03 | 0.501 | 0.784 | 1.000 | 19289 | tags=51%, list=35%, signal=79% | |
2422 | NEGATIVE REGULATION OF CALCIUM ION TRANSPORT INTO CYTOSOL | 36 | -0.28 | -1.02 | 0.410 | 0.785 | 1.000 | 19515 | tags=44%, list=36%, signal=69% | |
2423 | ENDOTHELIAL CELL ACTIVATION | 20 | -0.37 | -1.02 | 0.467 | 0.785 | 1.000 | 21755 | tags=60%, list=40%, signal=100% | |
2424 | REGULATION OF DNA METABOLIC PROCESS | 631 | -0.26 | -1.02 | 0.436 | 0.785 | 1.000 | 23271 | tags=49%, list=43%, signal=85% | |
2425 | GDP METABOLIC PROCESS | 25 | -0.34 | -1.02 | 0.472 | 0.785 | 1.000 | 20317 | tags=52%, list=37%, signal=83% | |
2426 | REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 383 | -0.26 | -1.02 | 0.467 | 0.785 | 1.000 | 29141 | tags=60%, list=53%, signal=128% | |
2427 | REGULATION OF NUCLEOTIDE-BINDING OLIGOMERIZATION DOMAIN CONTAINING SIGNALING PATHWAY | 20 | -0.38 | -1.02 | 0.454 | 0.785 | 1.000 | 23814 | tags=70%, list=44%, signal=124% | |
2428 | PEPTIDYL-LYSINE DIMETHYLATION | 25 | -0.33 | -1.02 | 0.424 | 0.785 | 1.000 | 26191 | tags=64%, list=48%, signal=123% | |
2429 | POSITIVE REGULATION OF RESPONSE TO BIOTIC STIMULUS | 64 | -0.27 | -1.02 | 0.433 | 0.785 | 1.000 | 17597 | tags=38%, list=32%, signal=55% | |
2430 | POSITIVE REGULATION OF DENDRITE MORPHOGENESIS | 47 | -0.27 | -1.02 | 0.448 | 0.785 | 1.000 | 26643 | tags=62%, list=49%, signal=120% | |
2431 | POSITIVE REGULATION OF MALE GONAD DEVELOPMENT | 9 | -0.40 | -1.02 | 0.436 | 0.785 | 1.000 | 18731 | tags=56%, list=34%, signal=84% | |
2432 | CELLULAR AMINO ACID BIOSYNTHETIC PROCESS | 128 | -0.26 | -1.02 | 0.447 | 0.785 | 1.000 | 27453 | tags=57%, list=50%, signal=114% | |
2433 | REGULATION OF STRESS FIBER ASSEMBLY | 136 | -0.27 | -1.02 | 0.455 | 0.784 | 1.000 | 30488 | tags=67%, list=56%, signal=151% | |
2434 | NEGATIVE REGULATION OF DOUBLE-STRAND BREAK REPAIR | 31 | -0.32 | -1.02 | 0.466 | 0.784 | 1.000 | 19300 | tags=48%, list=35%, signal=75% | |
2435 | REGULATION OF INTERLEUKIN-10 SECRETION | 16 | -0.40 | -1.02 | 0.470 | 0.786 | 1.000 | 22598 | tags=63%, list=41%, signal=106% | |
2436 | POSITIVE REGULATION OF MRNA 3'-END PROCESSING | 40 | -0.34 | -1.02 | 0.479 | 0.786 | 1.000 | 22173 | tags=60%, list=41%, signal=101% | |
2437 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION | 378 | -0.25 | -1.02 | 0.443 | 0.786 | 1.000 | 22653 | tags=45%, list=41%, signal=77% | |
2438 | POSITIVE REGULATION OF CARDIAC MUSCLE CONTRACTION | 16 | -0.37 | -1.02 | 0.425 | 0.785 | 1.000 | 15903 | tags=38%, list=29%, signal=53% | |
2439 | LIPOSACCHARIDE METABOLIC PROCESS | 201 | -0.27 | -1.02 | 0.429 | 0.785 | 1.000 | 22549 | tags=52%, list=41%, signal=89% | |
2440 | ENSHEATHMENT OF NEURONS | 109 | -0.27 | -1.02 | 0.478 | 0.785 | 1.000 | 23328 | tags=52%, list=43%, signal=91% | |
2441 | AXON ENSHEATHMENT | 109 | -0.27 | -1.02 | 0.478 | 0.785 | 1.000 | 23328 | tags=52%, list=43%, signal=91% | |
2442 | ESTABLISHMENT OF RNA LOCALIZATION | 206 | -0.29 | -1.02 | 0.490 | 0.785 | 1.000 | 23917 | tags=55%, list=44%, signal=98% | |
2443 | PROTEIN AUTOPROCESSING | 12 | -0.37 | -1.02 | 0.447 | 0.784 | 1.000 | 18320 | tags=58%, list=34%, signal=88% | |
2444 | VIRION ATTACHMENT TO HOST CELL | 22 | -0.35 | -1.02 | 0.453 | 0.784 | 1.000 | 25117 | tags=68%, list=46%, signal=126% | |
2445 | ADHESION OF SYMBIONT TO HOST CELL | 22 | -0.35 | -1.02 | 0.453 | 0.784 | 1.000 | 25117 | tags=68%, list=46%, signal=126% | |
2446 | REGULATION OF PROTEIN DEPOLYMERIZATION | 103 | -0.27 | -1.02 | 0.434 | 0.784 | 1.000 | 31888 | tags=68%, list=58%, signal=163% | |
2447 | REGULATION OF DEPHOSPHORYLATION | 328 | -0.27 | -1.02 | 0.446 | 0.784 | 1.000 | 31014 | tags=67%, list=57%, signal=155% | |
2448 | PHOSPHOLIPID DEPHOSPHORYLATION | 34 | -0.34 | -1.02 | 0.502 | 0.784 | 1.000 | 28707 | tags=74%, list=53%, signal=155% | |
2449 | PROTEIN ADP-RIBOSYLATION | 21 | -0.33 | -1.02 | 0.446 | 0.784 | 1.000 | 16235 | tags=43%, list=30%, signal=61% | |
2450 | XENOPHAGY | 203 | -0.26 | -1.02 | 0.435 | 0.784 | 1.000 | 27674 | tags=59%, list=51%, signal=118% | |
2451 | REGULATION OF PROTEIN K63-LINKED UBIQUITINATION | 20 | -0.34 | -1.02 | 0.470 | 0.784 | 1.000 | 29055 | tags=75%, list=53%, signal=160% | |
2452 | REGULATION OF PHOSPHATASE ACTIVITY | 280 | -0.27 | -1.02 | 0.478 | 0.783 | 1.000 | 29343 | tags=64%, list=54%, signal=137% | |
2453 | POSITIVE REGULATION OF P38MAPK CASCADE | 21 | -0.38 | -1.02 | 0.462 | 0.783 | 1.000 | 24937 | tags=71%, list=46%, signal=131% | |
2454 | POSITIVE REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 38 | -0.29 | -1.02 | 0.438 | 0.783 | 1.000 | 18901 | tags=42%, list=35%, signal=64% | |
2455 | REGULATION OF PROTEIN IMPORT INTO NUCLEUS | 305 | -0.25 | -1.02 | 0.477 | 0.783 | 1.000 | 29141 | tags=59%, list=53%, signal=125% | |
2456 | REGULATION OF NATURAL KILLER CELL MEDIATED CYTOTOXICITY | 59 | -0.30 | -1.02 | 0.443 | 0.783 | 1.000 | 16819 | tags=41%, list=31%, signal=59% | |
2457 | REGULATION OF TOOTH MINERALIZATION | 15 | -0.35 | -1.02 | 0.426 | 0.782 | 1.000 | 24219 | tags=53%, list=44%, signal=96% | |
2458 | RESPONSE TO GLUCAGON | 88 | -0.27 | -1.02 | 0.455 | 0.782 | 1.000 | 20922 | tags=44%, list=38%, signal=72% | |
2459 | REGULATION OF MRNA METABOLIC PROCESS | 242 | -0.29 | -1.02 | 0.455 | 0.782 | 1.000 | 21191 | tags=50%, list=39%, signal=81% | |
2460 | POSITIVE REGULATION OF EXECUTION PHASE OF APOPTOSIS | 21 | -0.35 | -1.02 | 0.444 | 0.782 | 1.000 | 17851 | tags=48%, list=33%, signal=71% | |
2461 | POSITIVE REGULATION OF CELLULAR SENESCENCE | 19 | -0.34 | -1.02 | 0.456 | 0.782 | 1.000 | 10308 | tags=32%, list=19%, signal=39% | |
2462 | CYTOPLASMIC SEQUESTERING OF TRANSCRIPTION FACTOR | 24 | -0.31 | -1.02 | 0.420 | 0.781 | 1.000 | 13714 | tags=33%, list=25%, signal=44% | |
2463 | REGULATION OF CELL DIVISION | 544 | -0.25 | -1.02 | 0.411 | 0.781 | 1.000 | 26241 | tags=55%, list=48%, signal=104% | |
2464 | DETECTION OF VISIBLE LIGHT | 217 | -0.24 | -1.02 | 0.412 | 0.781 | 1.000 | 19295 | tags=38%, list=35%, signal=59% | |
2465 | POSITIVE REGULATION OF FATTY ACID BETA-OXIDATION | 28 | -0.33 | -1.02 | 0.430 | 0.781 | 1.000 | 25689 | tags=61%, list=47%, signal=114% | |
2466 | CELLULAR RESPONSE TO HYDROGEN PEROXIDE | 55 | -0.29 | -1.02 | 0.432 | 0.781 | 1.000 | 15390 | tags=40%, list=28%, signal=56% | |
2467 | NEGATIVE REGULATION OF PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 31 | -0.32 | -1.02 | 0.475 | 0.780 | 1.000 | 22492 | tags=58%, list=41%, signal=99% | |
2468 | REGULATION OF PROTEIN KINASE B SIGNALING | 190 | -0.25 | -1.02 | 0.446 | 0.781 | 1.000 | 28911 | tags=58%, list=53%, signal=122% | |
2469 | DETERMINATION OF ADULT LIFESPAN | 10 | -0.42 | -1.02 | 0.469 | 0.781 | 1.000 | 14322 | tags=50%, list=26%, signal=68% | |
2470 | NEGATIVE REGULATION OF DNA BIOSYNTHETIC PROCESS | 63 | -0.28 | -1.02 | 0.436 | 0.781 | 1.000 | 22427 | tags=46%, list=41%, signal=78% | |
2471 | CELLULAR RESPONSE TO PH | 27 | -0.31 | -1.02 | 0.434 | 0.781 | 1.000 | 33277 | tags=81%, list=61%, signal=208% | |
2472 | POSITIVE REGULATION OF TRANSLATION | 166 | -0.28 | -1.02 | 0.451 | 0.781 | 1.000 | 23644 | tags=54%, list=43%, signal=95% | |
2473 | NEUROMUSCULAR JUNCTION DEVELOPMENT | 23 | -0.34 | -1.02 | 0.464 | 0.781 | 1.000 | 23256 | tags=57%, list=43%, signal=98% | |
2474 | POSITIVE REGULATION OF CELLULAR AMIDE METABOLIC PROCESS | 194 | -0.28 | -1.02 | 0.482 | 0.782 | 1.000 | 23644 | tags=54%, list=43%, signal=95% | |
2475 | O-GLYCAN PROCESSING | 133 | -0.26 | -1.02 | 0.451 | 0.781 | 1.000 | 25708 | tags=52%, list=47%, signal=98% | |
2476 | POSITIVE REGULATION OF PROTEIN POLYUBIQUITINATION | 16 | -0.38 | -1.02 | 0.453 | 0.781 | 1.000 | 25657 | tags=69%, list=47%, signal=129% | |
2477 | REGULATION OF TRANSLATIONAL INITIATION IN RESPONSE TO STRESS | 27 | -0.35 | -1.02 | 0.479 | 0.781 | 1.000 | 29221 | tags=81%, list=53%, signal=175% | |
2478 | REGULATION OF ENTRY OF BACTERIUM INTO HOST CELL | 11 | -0.38 | -1.02 | 0.442 | 0.781 | 1.000 | 22063 | tags=64%, list=40%, signal=107% | |
2479 | CRANIAL NERVE DEVELOPMENT | 32 | -0.30 | -1.02 | 0.444 | 0.781 | 1.000 | 24652 | tags=56%, list=45%, signal=102% | |
2480 | POSITIVE REGULATION OF PEPTIDYL-SERINE PHOSPHORYLATION | 128 | -0.28 | -1.02 | 0.472 | 0.780 | 1.000 | 20622 | tags=47%, list=38%, signal=75% | |
2481 | MRNA EXPORT FROM NUCLEUS | 170 | -0.30 | -1.02 | 0.486 | 0.780 | 1.000 | 22894 | tags=54%, list=42%, signal=93% | |
2482 | MRNA-CONTAINING RIBONUCLEOPROTEIN COMPLEX EXPORT FROM NUCLEUS | 170 | -0.30 | -1.02 | 0.486 | 0.780 | 1.000 | 22894 | tags=54%, list=42%, signal=93% | |
2483 | PROTEIN TETRAMERIZATION | 194 | -0.27 | -1.02 | 0.478 | 0.781 | 1.000 | 25118 | tags=56%, list=46%, signal=103% | |
2484 | PRODUCTION OF SIRNA INVOLVED IN RNA INTERFERENCE | 11 | -0.38 | -1.02 | 0.447 | 0.780 | 1.000 | 32076 | tags=91%, list=59%, signal=220% | |
2485 | REGULATION OF GTPASE ACTIVITY | 854 | -0.24 | -1.02 | 0.495 | 0.780 | 1.000 | 28781 | tags=56%, list=53%, signal=116% | |
2486 | RESPONSE TO VIRUS | 331 | -0.27 | -1.02 | 0.496 | 0.780 | 1.000 | 23343 | tags=52%, list=43%, signal=90% | |
2487 | SPHINGOLIPID CATABOLIC PROCESS | 19 | -0.35 | -1.02 | 0.454 | 0.780 | 1.000 | 14671 | tags=42%, list=27%, signal=58% | |
2488 | IRON COORDINATION ENTITY TRANSPORT | 15 | -0.35 | -1.02 | 0.454 | 0.780 | 1.000 | 28338 | tags=73%, list=52%, signal=152% | |
2489 | HIGH-DENSITY LIPOPROTEIN PARTICLE REMODELING | 29 | -0.32 | -1.02 | 0.460 | 0.780 | 1.000 | 16531 | tags=38%, list=30%, signal=54% | |
2490 | ADHESION OF SYMBIONT TO HOST | 27 | -0.34 | -1.02 | 0.438 | 0.780 | 1.000 | 25117 | tags=63%, list=46%, signal=116% | |
2491 | NEGATIVE REGULATION OF DENDRITIC SPINE DEVELOPMENT | 20 | -0.38 | -1.02 | 0.463 | 0.780 | 1.000 | 26579 | tags=80%, list=49%, signal=156% | |
2492 | DNA LIGATION | 24 | -0.33 | -1.02 | 0.472 | 0.780 | 1.000 | 27915 | tags=63%, list=51%, signal=128% | |
2493 | POSITIVE REGULATION OF HISTONE DEACETYLATION | 33 | -0.32 | -1.02 | 0.494 | 0.780 | 1.000 | 12000 | tags=36%, list=22%, signal=47% | |
2494 | REGULATION OF ADIPONECTIN SECRETION | 14 | -0.40 | -1.02 | 0.448 | 0.780 | 1.000 | 25066 | tags=71%, list=46%, signal=132% | |
2495 | POSITIVE REGULATION OF ATPASE ACTIVITY | 76 | -0.28 | -1.02 | 0.480 | 0.780 | 1.000 | 22376 | tags=50%, list=41%, signal=85% | |
2496 | RECEPTOR METABOLIC PROCESS | 145 | -0.28 | -1.02 | 0.461 | 0.781 | 1.000 | 22297 | tags=49%, list=41%, signal=82% | |
2497 | TRABECULA MORPHOGENESIS | 39 | -0.28 | -1.02 | 0.433 | 0.780 | 1.000 | 25055 | tags=54%, list=46%, signal=99% | |
2498 | NUCLEOBASE-CONTAINING COMPOUND TRANSPORT | 242 | -0.28 | -1.02 | 0.471 | 0.781 | 1.000 | 23917 | tags=54%, list=44%, signal=96% | |
2499 | PATHWAY-RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 24 | -0.33 | -1.02 | 0.451 | 0.781 | 1.000 | 21755 | tags=50%, list=40%, signal=83% | |
2500 | REGULATION OF ENDOPEPTIDASE ACTIVITY | 643 | -0.26 | -1.02 | 0.496 | 0.781 | 1.000 | 20684 | tags=46%, list=38%, signal=73% | |
2501 | POSITIVE REGULATION OF CYCLIN-DEPENDENT PROTEIN SERINE/THREONINE KINASE ACTIVITY INVOLVED IN G1/S TRANSITION OF MITOTIC CELL CYCLE | 24 | -0.31 | -1.02 | 0.487 | 0.781 | 1.000 | 15550 | tags=38%, list=28%, signal=52% | |
2502 | RNA EXPORT FROM NUCLEUS | 179 | -0.30 | -1.02 | 0.499 | 0.781 | 1.000 | 23917 | tags=56%, list=44%, signal=100% | |
2503 | MICROTUBULE BUNDLE FORMATION | 104 | -0.30 | -1.02 | 0.460 | 0.781 | 1.000 | 21543 | tags=52%, list=39%, signal=86% | |
2504 | VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 760 | -0.23 | -1.02 | 0.490 | 0.781 | 1.000 | 22198 | tags=44%, list=41%, signal=73% | |
2505 | TRANSMEMBRANE RECEPTOR PROTEIN SERINE/THREONINE KINASE SIGNALING PATHWAY | 421 | -0.26 | -1.02 | 0.453 | 0.781 | 1.000 | 22260 | tags=48%, list=41%, signal=80% | |
2506 | ENDOPLASMIC RETICULUM CALCIUM ION HOMEOSTASIS | 52 | -0.29 | -1.02 | 0.446 | 0.781 | 1.000 | 15030 | tags=38%, list=27%, signal=53% | |
2507 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 252 | -0.25 | -1.02 | 0.466 | 0.781 | 1.000 | 20480 | tags=43%, list=37%, signal=69% | |
2508 | DEMETHYLATION | 104 | -0.27 | -1.02 | 0.475 | 0.781 | 1.000 | 30398 | tags=66%, list=56%, signal=149% | |
2509 | TRIGLYCERIDE METABOLIC PROCESS | 183 | -0.25 | -1.02 | 0.453 | 0.780 | 1.000 | 24351 | tags=51%, list=45%, signal=91% | |
2510 | SPHINGOMYELIN METABOLIC PROCESS | 14 | -0.37 | -1.02 | 0.454 | 0.780 | 1.000 | 32608 | tags=86%, list=60%, signal=212% | |
2511 | GROWTH HORMONE SECRETION | 17 | -0.34 | -1.02 | 0.455 | 0.781 | 1.000 | 15793 | tags=35%, list=29%, signal=50% | |
2512 | OXALATE TRANSPORT | 9 | -0.40 | -1.02 | 0.424 | 0.781 | 1.000 | 1498 | tags=22%, list=3%, signal=23% | |
2513 | PROTEIN OLIGOMERIZATION | 565 | -0.26 | -1.02 | 0.489 | 0.781 | 1.000 | 22724 | tags=48%, list=42%, signal=82% | |
2514 | CELLULAR RESPONSE TO GLUCOSE STIMULUS | 38 | -0.32 | -1.01 | 0.506 | 0.781 | 1.000 | 22892 | tags=61%, list=42%, signal=104% | |
2515 | REGULATION OF PRI-MIRNA TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 45 | -0.31 | -1.01 | 0.505 | 0.782 | 1.000 | 30975 | tags=76%, list=57%, signal=174% | |
2516 | REGULATION OF CELL PROJECTION ORGANIZATION | 729 | -0.24 | -1.01 | 0.515 | 0.781 | 1.000 | 29430 | tags=59%, list=54%, signal=125% | |
2517 | POSITIVE REGULATION OF HISTONE METHYLATION | 63 | -0.31 | -1.01 | 0.495 | 0.781 | 1.000 | 15797 | tags=41%, list=29%, signal=58% | |
2518 | TETRAHYDROFOLATE INTERCONVERSION | 16 | -0.38 | -1.01 | 0.467 | 0.781 | 1.000 | 26219 | tags=69%, list=48%, signal=132% | |
2519 | NUCLEOTIDE-SUGAR BIOSYNTHETIC PROCESS | 27 | -0.35 | -1.01 | 0.500 | 0.781 | 1.000 | 20380 | tags=59%, list=37%, signal=94% | |
2520 | VITAMIN METABOLIC PROCESS | 332 | -0.25 | -1.01 | 0.444 | 0.781 | 1.000 | 19714 | tags=41%, list=36%, signal=63% | |
2521 | PROTEIN LOCALIZATION TO CHROMOSOME | 74 | -0.30 | -1.01 | 0.482 | 0.780 | 1.000 | 24641 | tags=55%, list=45%, signal=101% | |
2522 | REGULATION OF MYELOID LEUKOCYTE MEDIATED IMMUNITY | 41 | -0.32 | -1.01 | 0.434 | 0.780 | 1.000 | 12087 | tags=32%, list=22%, signal=41% | |
2523 | KERATAN SULFATE METABOLIC PROCESS | 82 | -0.27 | -1.01 | 0.456 | 0.780 | 1.000 | 17152 | tags=38%, list=31%, signal=55% | |
2524 | REGULATION OF DEFENSE RESPONSE TO VIRUS BY HOST | 254 | -0.25 | -1.01 | 0.444 | 0.780 | 1.000 | 24264 | tags=51%, list=44%, signal=91% | |
2525 | BILE ACID METABOLIC PROCESS | 78 | -0.29 | -1.01 | 0.477 | 0.780 | 1.000 | 31508 | tags=71%, list=58%, signal=166% | |
2526 | HEPARAN SULFATE PROTEOGLYCAN METABOLIC PROCESS | 23 | -0.35 | -1.01 | 0.487 | 0.780 | 1.000 | 21898 | tags=61%, list=40%, signal=101% | |
2527 | SOMATIC DIVERSIFICATION OF IMMUNE RECEPTORS | 59 | -0.28 | -1.01 | 0.458 | 0.780 | 1.000 | 18286 | tags=42%, list=33%, signal=64% | |
2528 | POSITIVE REGULATION OF NIK/NF-KAPPAB SIGNALING | 40 | -0.30 | -1.01 | 0.460 | 0.780 | 1.000 | 23080 | tags=58%, list=42%, signal=99% | |
2529 | CELLULAR RESPONSE TO GLUCAGON STIMULUS | 80 | -0.27 | -1.01 | 0.440 | 0.780 | 1.000 | 20922 | tags=44%, list=38%, signal=71% | |
2530 | PROTEIN HEXAMERIZATION | 8 | -0.40 | -1.01 | 0.437 | 0.780 | 1.000 | 21083 | tags=63%, list=39%, signal=102% | |
2531 | MITOTIC G2/M TRANSITION CHECKPOINT | 41 | -0.31 | -1.01 | 0.459 | 0.781 | 1.000 | 14139 | tags=34%, list=26%, signal=46% | |
2532 | POSITIVE REGULATION OF LIPOPOLYSACCHARIDE-MEDIATED SIGNALING PATHWAY | 13 | -0.40 | -1.01 | 0.472 | 0.781 | 1.000 | 21017 | tags=54%, list=38%, signal=87% | |
2533 | OVARIAN FOLLICLE DEVELOPMENT | 24 | -0.35 | -1.01 | 0.484 | 0.781 | 1.000 | 6539 | tags=29%, list=12%, signal=33% | |
2534 | ORGANELLE ASSEMBLY | 749 | -0.27 | -1.01 | 0.485 | 0.781 | 1.000 | 27719 | tags=61%, list=51%, signal=123% | |
2535 | STEROL BIOSYNTHETIC PROCESS | 60 | -0.31 | -1.01 | 0.451 | 0.781 | 1.000 | 28192 | tags=68%, list=52%, signal=141% | |
2536 | PLACENTA DEVELOPMENT | 80 | -0.26 | -1.01 | 0.460 | 0.782 | 1.000 | 25953 | tags=55%, list=47%, signal=105% | |
2537 | DEVELOPMENTAL PIGMENTATION | 41 | -0.31 | -1.01 | 0.444 | 0.782 | 1.000 | 17854 | tags=41%, list=33%, signal=62% | |
2538 | NEGATIVE REGULATION OF PROTEIN PHOSPHORYLATION | 645 | -0.25 | -1.01 | 0.533 | 0.782 | 1.000 | 27121 | tags=56%, list=50%, signal=110% | |
2539 | NEGATIVE REGULATION OF DEFENSE RESPONSE TO VIRUS | 33 | -0.34 | -1.01 | 0.499 | 0.783 | 1.000 | 27936 | tags=73%, list=51%, signal=149% | |
2540 | SEMAPHORIN-PLEXIN SIGNALING PATHWAY | 54 | -0.29 | -1.01 | 0.437 | 0.783 | 1.000 | 4831 | tags=20%, list=9%, signal=22% | |
2541 | LIPID LOCALIZATION | 304 | -0.25 | -1.01 | 0.457 | 0.783 | 1.000 | 24104 | tags=49%, list=44%, signal=88% | |
2542 | NEGATIVE REGULATION OF VIRAL GENOME REPLICATION | 107 | -0.29 | -1.01 | 0.463 | 0.783 | 1.000 | 8722 | tags=28%, list=16%, signal=33% | |
2543 | CEREBRAL CORTEX RADIAL GLIA GUIDED MIGRATION | 22 | -0.36 | -1.01 | 0.449 | 0.783 | 1.000 | 11496 | tags=36%, list=21%, signal=46% | |
2544 | TELENCEPHALON GLIAL CELL MIGRATION | 22 | -0.36 | -1.01 | 0.449 | 0.783 | 1.000 | 11496 | tags=36%, list=21%, signal=46% | |
2545 | NUCLEOTIDE-SUGAR METABOLIC PROCESS | 48 | -0.32 | -1.01 | 0.502 | 0.783 | 1.000 | 21261 | tags=56%, list=39%, signal=92% | |
2546 | REGULATION OF PEPTIDASE ACTIVITY | 661 | -0.26 | -1.01 | 0.508 | 0.783 | 1.000 | 20684 | tags=46%, list=38%, signal=73% | |
2547 | MEMBRANE LIPID METABOLIC PROCESS | 315 | -0.27 | -1.01 | 0.486 | 0.783 | 1.000 | 24401 | tags=54%, list=45%, signal=97% | |
2548 | NEGATIVE REGULATION OF HYDROLASE ACTIVITY | 695 | -0.25 | -1.01 | 0.483 | 0.783 | 1.000 | 20653 | tags=43%, list=38%, signal=68% | |
2549 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 172 | -0.27 | -1.01 | 0.490 | 0.783 | 1.000 | 20002 | tags=43%, list=37%, signal=68% | |
2550 | POSITIVE REGULATION OF TRIGLYCERIDE LIPASE ACTIVITY | 13 | -0.42 | -1.01 | 0.457 | 0.783 | 1.000 | 4646 | tags=23%, list=8%, signal=25% | |
2551 | ORGANONITROGEN COMPOUND CATABOLIC PROCESS | 601 | -0.24 | -1.01 | 0.469 | 0.785 | 1.000 | 26115 | tags=52%, list=48%, signal=98% | |
2552 | CENTROSOME LOCALIZATION | 30 | -0.33 | -1.01 | 0.446 | 0.785 | 1.000 | 24311 | tags=57%, list=44%, signal=102% | |
2553 | CELLULAR RESPONSE TO OXIDATIVE STRESS | 234 | -0.26 | -1.01 | 0.495 | 0.784 | 1.000 | 23310 | tags=49%, list=43%, signal=85% | |
2554 | DECIDUALIZATION | 15 | -0.36 | -1.01 | 0.475 | 0.784 | 1.000 | 15325 | tags=40%, list=28%, signal=56% | |
2555 | HISTONE DEMETHYLATION | 48 | -0.30 | -1.01 | 0.472 | 0.784 | 1.000 | 30398 | tags=69%, list=56%, signal=155% | |
2556 | INTERFERON-GAMMA-MEDIATED SIGNALING PATHWAY | 222 | -0.27 | -1.01 | 0.443 | 0.784 | 1.000 | 26963 | tags=59%, list=49%, signal=117% | |
2557 | RESPONSE TO GLUCOCORTICOID | 46 | -0.30 | -1.01 | 0.469 | 0.784 | 1.000 | 20883 | tags=43%, list=38%, signal=70% | |
2558 | ATRIOVENTRICULAR VALVE DEVELOPMENT | 28 | -0.31 | -1.01 | 0.470 | 0.784 | 1.000 | 25051 | tags=54%, list=46%, signal=99% | |
2559 | REGULATION OF RESPIRATORY BURST | 49 | -0.30 | -1.01 | 0.477 | 0.784 | 1.000 | 13099 | tags=29%, list=24%, signal=38% | |
2560 | JAK-STAT CASCADE INVOLVED IN GROWTH HORMONE SIGNALING PATHWAY | 80 | -0.29 | -1.01 | 0.458 | 0.784 | 1.000 | 26401 | tags=55%, list=48%, signal=106% | |
2561 | CHOLESTEROL TRANSPORT | 85 | -0.28 | -1.01 | 0.451 | 0.785 | 1.000 | 21720 | tags=45%, list=40%, signal=74% | |
2562 | CELL-SUBSTRATE JUNCTION ASSEMBLY | 85 | -0.26 | -1.01 | 0.474 | 0.785 | 1.000 | 14948 | tags=34%, list=27%, signal=47% | |
2563 | REGULATION OF ACTIVATED T CELL PROLIFERATION | 58 | -0.26 | -1.01 | 0.467 | 0.785 | 1.000 | 13287 | tags=31%, list=24%, signal=41% | |
2564 | REGULATION OF NEURON APOPTOTIC PROCESS | 194 | -0.26 | -1.01 | 0.494 | 0.785 | 1.000 | 26505 | tags=55%, list=48%, signal=107% | |
2565 | NEGATIVE REGULATION OF CELL PROJECTION ORGANIZATION | 167 | -0.26 | -1.01 | 0.511 | 0.786 | 1.000 | 28569 | tags=59%, list=52%, signal=124% | |
2566 | REGULATION OF MYELOID CELL APOPTOTIC PROCESS | 20 | -0.32 | -1.01 | 0.448 | 0.786 | 1.000 | 28092 | tags=70%, list=51%, signal=144% | |
2567 | NEGATIVE REGULATION OF PROTEIN SUMOYLATION | 14 | -0.39 | -1.01 | 0.462 | 0.786 | 1.000 | 25955 | tags=71%, list=47%, signal=136% | |
2568 | MITOTIC RECOMBINATION | 58 | -0.32 | -1.01 | 0.507 | 0.786 | 1.000 | 22940 | tags=59%, list=42%, signal=101% | |
2569 | REGULATION OF PROTEIN DEPHOSPHORYLATION | 318 | -0.26 | -1.01 | 0.468 | 0.786 | 1.000 | 31014 | tags=67%, list=57%, signal=155% | |
2570 | ESTABLISHMENT OF MITOCHONDRION LOCALIZATION, MICROTUBULE-MEDIATED | 22 | -0.34 | -1.01 | 0.438 | 0.787 | 1.000 | 26112 | tags=68%, list=48%, signal=130% | |
2571 | MITOCHONDRION TRANSPORT ALONG MICROTUBULE | 22 | -0.34 | -1.01 | 0.438 | 0.786 | 1.000 | 26112 | tags=68%, list=48%, signal=130% | |
2572 | ESTABLISHMENT OF MITOCHONDRION LOCALIZATION | 22 | -0.34 | -1.01 | 0.438 | 0.786 | 1.000 | 26112 | tags=68%, list=48%, signal=130% | |
2573 | VITAMIN K METABOLIC PROCESS | 10 | -0.45 | -1.01 | 0.467 | 0.786 | 1.000 | 11992 | tags=50%, list=22%, signal=64% | |
2574 | ACTIN CYTOSKELETON ORGANIZATION | 655 | -0.24 | -1.01 | 0.485 | 0.786 | 1.000 | 19032 | tags=40%, list=35%, signal=61% | |
2575 | ENDOPLASMIC RETICULUM ORGANIZATION | 71 | -0.29 | -1.01 | 0.492 | 0.786 | 1.000 | 27141 | tags=62%, list=50%, signal=123% | |
2576 | POSITIVE REGULATION OF LIPID BIOSYNTHETIC PROCESS | 102 | -0.26 | -1.01 | 0.449 | 0.787 | 1.000 | 17124 | tags=36%, list=31%, signal=53% | |
2577 | REGULATION OF INTERLEUKIN-4 PRODUCTION | 43 | -0.32 | -1.01 | 0.466 | 0.787 | 1.000 | 22721 | tags=47%, list=42%, signal=80% | |
2578 | PHOTOTRANSDUCTION | 217 | -0.23 | -1.01 | 0.447 | 0.787 | 1.000 | 19295 | tags=38%, list=35%, signal=59% | |
2579 | REGULATION OF TRANSLATION IN RESPONSE TO STRESS | 47 | -0.32 | -1.00 | 0.504 | 0.788 | 1.000 | 30846 | tags=79%, list=56%, signal=180% | |
2580 | REGULATION OF SPINDLE ORGANIZATION | 40 | -0.33 | -1.00 | 0.469 | 0.787 | 1.000 | 18914 | tags=52%, list=35%, signal=80% | |
2581 | SPERMATID DEVELOPMENT | 73 | -0.25 | -1.00 | 0.476 | 0.787 | 1.000 | 24273 | tags=48%, list=44%, signal=86% | |
2582 | POSITIVE REGULATION OF TUMOR NECROSIS FACTOR PRODUCTION | 76 | -0.29 | -1.00 | 0.463 | 0.788 | 1.000 | 16757 | tags=39%, list=31%, signal=57% | |
2583 | NEGATIVE REGULATION OF CELLULAR CARBOHYDRATE METABOLIC PROCESS | 62 | -0.28 | -1.00 | 0.459 | 0.788 | 1.000 | 28882 | tags=60%, list=53%, signal=126% | |
2584 | ATTACHMENT OF GPI ANCHOR TO PROTEIN | 18 | -0.37 | -1.00 | 0.502 | 0.788 | 1.000 | 24812 | tags=72%, list=45%, signal=132% | |
2585 | RIBONUCLEOPROTEIN COMPLEX DISASSEMBLY | 26 | -0.36 | -1.00 | 0.459 | 0.788 | 1.000 | 20798 | tags=62%, list=38%, signal=99% | |
2586 | ETHANOL METABOLIC PROCESS | 25 | -0.30 | -1.00 | 0.455 | 0.788 | 1.000 | 1950 | tags=16%, list=4%, signal=17% | |
2587 | ETHANOL OXIDATION | 25 | -0.30 | -1.00 | 0.455 | 0.788 | 1.000 | 1950 | tags=16%, list=4%, signal=17% | |
2588 | NEGATIVE REGULATION OF TRANSPORTER ACTIVITY | 122 | -0.26 | -1.00 | 0.488 | 0.788 | 1.000 | 28741 | tags=59%, list=53%, signal=124% | |
2589 | INNER EAR MORPHOGENESIS | 59 | -0.27 | -1.00 | 0.455 | 0.788 | 1.000 | 29991 | tags=59%, list=55%, signal=131% | |
2590 | NEGATIVE REGULATION OF TYPE 2 IMMUNE RESPONSE | 10 | -0.40 | -1.00 | 0.479 | 0.788 | 1.000 | 27087 | tags=70%, list=50%, signal=139% | |
2591 | REGULATION OF FATTY ACID METABOLIC PROCESS | 147 | -0.26 | -1.00 | 0.473 | 0.788 | 1.000 | 29187 | tags=61%, list=53%, signal=131% | |
2592 | CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 347 | -0.26 | -1.00 | 0.469 | 0.788 | 1.000 | 20835 | tags=46%, list=38%, signal=74% | |
2593 | MELANOSOME LOCALIZATION | 35 | -0.34 | -1.00 | 0.493 | 0.788 | 1.000 | 11866 | tags=40%, list=22%, signal=51% | |
2594 | PIGMENT GRANULE LOCALIZATION | 35 | -0.34 | -1.00 | 0.493 | 0.788 | 1.000 | 11866 | tags=40%, list=22%, signal=51% | |
2595 | REGULATION OF CYTOKINE PRODUCTION | 986 | -0.25 | -1.00 | 0.501 | 0.787 | 1.000 | 22858 | tags=45%, list=42%, signal=77% | |
2596 | TELOMERE MAINTENANCE VIA SEMI-CONSERVATIVE REPLICATION | 45 | -0.31 | -1.00 | 0.502 | 0.787 | 1.000 | 22812 | tags=58%, list=42%, signal=99% | |
2597 | REGULATION OF CHROMATIN SILENCING | 20 | -0.33 | -1.00 | 0.459 | 0.787 | 1.000 | 15434 | tags=35%, list=28%, signal=49% | |
2598 | PROTEIN K63-LINKED DEUBIQUITINATION | 64 | -0.30 | -1.00 | 0.455 | 0.788 | 1.000 | 23060 | tags=55%, list=42%, signal=94% | |
2599 | NEGATIVE REGULATION OF GENE SILENCING | 20 | -0.35 | -1.00 | 0.454 | 0.788 | 1.000 | 6172 | tags=25%, list=11%, signal=28% | |
2600 | IMPORT INTO CELL | 57 | -0.30 | -1.00 | 0.466 | 0.788 | 1.000 | 14921 | tags=37%, list=27%, signal=51% | |
2601 | POSITIVE REGULATION OF CHOLESTEROL ESTERIFICATION | 13 | -0.42 | -1.00 | 0.477 | 0.788 | 1.000 | 19183 | tags=54%, list=35%, signal=83% | |
2602 | SIGNAL TRANSDUCTION BY PROTEIN PHOSPHORYLATION | 816 | -0.23 | -1.00 | 0.516 | 0.788 | 1.000 | 26839 | tags=53%, list=49%, signal=103% | |
2603 | REGULATION OF ATTACHMENT OF SPINDLE MICROTUBULES TO KINETOCHORE | 26 | -0.36 | -1.00 | 0.499 | 0.788 | 1.000 | 31761 | tags=88%, list=58%, signal=211% | |
2604 | NEGATIVE REGULATION OF PROTEIN DEPOLYMERIZATION | 68 | -0.28 | -1.00 | 0.489 | 0.789 | 1.000 | 31885 | tags=69%, list=58%, signal=166% | |
2605 | REGULATION OF CELL MORPHOGENESIS | 858 | -0.24 | -1.00 | 0.529 | 0.788 | 1.000 | 27838 | tags=56%, list=51%, signal=112% | |
2606 | NEGATIVE REGULATION OF PROTEIN COMPLEX DISASSEMBLY | 76 | -0.27 | -1.00 | 0.525 | 0.789 | 1.000 | 31885 | tags=68%, list=58%, signal=164% | |
2607 | REGULATION OF POSTTRANSCRIPTIONAL GENE SILENCING | 28 | -0.30 | -1.00 | 0.487 | 0.789 | 1.000 | 27407 | tags=64%, list=50%, signal=129% | |
2608 | REGULATION OF GENE SILENCING BY RNA | 28 | -0.30 | -1.00 | 0.487 | 0.789 | 1.000 | 27407 | tags=64%, list=50%, signal=129% | |
2609 | CELL JUNCTION MAINTENANCE | 9 | -0.40 | -1.00 | 0.469 | 0.789 | 1.000 | 22748 | tags=67%, list=42%, signal=114% | |
2610 | CHROMATIN REMODELING | 270 | -0.26 | -1.00 | 0.484 | 0.789 | 1.000 | 13733 | tags=34%, list=25%, signal=46% | |
2611 | POSITIVE REGULATION OF DEFENSE RESPONSE TO BACTERIUM | 10 | -0.38 | -1.00 | 0.470 | 0.789 | 1.000 | 11195 | tags=30%, list=20%, signal=38% | |
2612 | PROTEIN POLYMERIZATION | 127 | -0.29 | -1.00 | 0.503 | 0.789 | 1.000 | 19289 | tags=48%, list=35%, signal=74% | |
2613 | QUINONE METABOLIC PROCESS | 49 | -0.33 | -1.00 | 0.487 | 0.789 | 1.000 | 28279 | tags=73%, list=52%, signal=152% | |
2614 | POSITIVE REGULATION OF RNA SPLICING | 47 | -0.28 | -1.00 | 0.467 | 0.788 | 1.000 | 24285 | tags=51%, list=44%, signal=92% | |
2615 | OSTEOBLAST DIFFERENTIATION | 196 | -0.25 | -1.00 | 0.481 | 0.789 | 1.000 | 28737 | tags=58%, list=53%, signal=122% | |
2616 | REGULATION OF PROTEIN IMPORT INTO NUCLEUS, TRANSLOCATION | 27 | -0.31 | -1.00 | 0.481 | 0.789 | 1.000 | 19300 | tags=48%, list=35%, signal=74% | |
2617 | REGULATION OF PROTEIN GLYCOSYLATION | 18 | -0.36 | -1.00 | 0.497 | 0.789 | 1.000 | 18947 | tags=56%, list=35%, signal=85% | |
2618 | MAPK CASCADE | 791 | -0.23 | -1.00 | 0.514 | 0.788 | 1.000 | 26839 | tags=53%, list=49%, signal=102% | |
2619 | APOPTOTIC MITOCHONDRIAL CHANGES | 79 | -0.28 | -1.00 | 0.488 | 0.788 | 1.000 | 21395 | tags=48%, list=39%, signal=79% | |
2620 | COPPER ION TRANSMEMBRANE TRANSPORT | 11 | -0.43 | -1.00 | 0.496 | 0.788 | 1.000 | 22042 | tags=73%, list=40%, signal=122% | |
2621 | REGULATION OF HIPPO SIGNALING | 36 | -0.31 | -1.00 | 0.478 | 0.788 | 1.000 | 22779 | tags=53%, list=42%, signal=90% | |
2622 | REGULATION OF CENTRIOLE REPLICATION | 27 | -0.35 | -1.00 | 0.479 | 0.788 | 1.000 | 26834 | tags=70%, list=49%, signal=138% | |
2623 | METHIONINE METABOLIC PROCESS | 32 | -0.32 | -1.00 | 0.502 | 0.788 | 1.000 | 27293 | tags=69%, list=50%, signal=137% | |
2624 | PERK-MEDIATED UNFOLDED PROTEIN RESPONSE | 23 | -0.33 | -1.00 | 0.461 | 0.788 | 1.000 | 13724 | tags=35%, list=25%, signal=46% | |
2625 | NEURONAL STEM CELL DIVISION | 27 | -0.31 | -1.00 | 0.455 | 0.789 | 1.000 | 21813 | tags=52%, list=40%, signal=86% | |
2626 | NEUROBLAST DIVISION | 27 | -0.31 | -1.00 | 0.455 | 0.788 | 1.000 | 21813 | tags=52%, list=40%, signal=86% | |
2627 | RESPONSE TO ACID CHEMICAL | 277 | -0.24 | -1.00 | 0.499 | 0.789 | 1.000 | 18886 | tags=39%, list=35%, signal=60% | |
2628 | NEGATIVE REGULATION OF MONOOXYGENASE ACTIVITY | 16 | -0.35 | -1.00 | 0.452 | 0.789 | 1.000 | 14129 | tags=38%, list=26%, signal=51% | |
2629 | CARDIAC SEPTUM DEVELOPMENT | 103 | -0.25 | -1.00 | 0.490 | 0.789 | 1.000 | 14036 | tags=31%, list=26%, signal=42% | |
2630 | REGULATION OF CENTROSOME CYCLE | 75 | -0.29 | -1.00 | 0.480 | 0.789 | 1.000 | 27474 | tags=63%, list=50%, signal=126% | |
2631 | PINOCYTOSIS | 21 | -0.35 | -1.00 | 0.484 | 0.789 | 1.000 | 11904 | tags=38%, list=22%, signal=49% | |
2632 | RESPONSE TO INTERFERON-GAMMA | 318 | -0.26 | -1.00 | 0.479 | 0.789 | 1.000 | 24701 | tags=54%, list=45%, signal=98% | |
2633 | KYNURENINE METABOLIC PROCESS | 9 | -0.42 | -1.00 | 0.494 | 0.789 | 1.000 | 30919 | tags=89%, list=57%, signal=205% | |
2634 | RESPONSE TO NICOTINE | 24 | -0.33 | -1.00 | 0.450 | 0.788 | 1.000 | 17667 | tags=42%, list=32%, signal=62% | |
2635 | RNA SURVEILLANCE | 11 | -0.40 | -1.00 | 0.486 | 0.789 | 1.000 | 29604 | tags=91%, list=54%, signal=198% | |
2636 | EMBRYO IMPLANTATION | 34 | -0.30 | -1.00 | 0.491 | 0.789 | 1.000 | 18771 | tags=41%, list=34%, signal=63% | |
2637 | MODULATION BY HOST OF VIRAL RELEASE FROM HOST CELL | 14 | -0.38 | -1.00 | 0.496 | 0.788 | 1.000 | 20245 | tags=57%, list=37%, signal=91% | |
2638 | POSITIVE REGULATION BY HOST OF VIRAL RELEASE FROM HOST CELL | 14 | -0.38 | -1.00 | 0.496 | 0.788 | 1.000 | 20245 | tags=57%, list=37%, signal=91% | |
2639 | INSULIN-LIKE GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 25 | -0.34 | -1.00 | 0.501 | 0.788 | 1.000 | 11665 | tags=40%, list=21%, signal=51% | |
2640 | DETECTION OF LIGHT STIMULUS | 224 | -0.23 | -1.00 | 0.452 | 0.788 | 1.000 | 19295 | tags=38%, list=35%, signal=58% | |
2641 | OSSIFICATION | 269 | -0.24 | -1.00 | 0.520 | 0.788 | 1.000 | 29340 | tags=58%, list=54%, signal=125% | |
2642 | MUSCLE CELL MIGRATION | 33 | -0.30 | -1.00 | 0.478 | 0.788 | 1.000 | 21303 | tags=52%, list=39%, signal=84% | |
2643 | NEGATIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 926 | -0.24 | -1.00 | 0.543 | 0.788 | 1.000 | 22260 | tags=46%, list=41%, signal=76% | |
2644 | NEGATIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 926 | -0.24 | -1.00 | 0.543 | 0.787 | 1.000 | 22260 | tags=46%, list=41%, signal=76% | |
2645 | MODIFICATION BY HOST OF SYMBIONT MORPHOLOGY OR PHYSIOLOGY | 107 | -0.27 | -1.00 | 0.498 | 0.788 | 1.000 | 20339 | tags=46%, list=37%, signal=73% | |
2646 | PURINE NUCLEOTIDE CATABOLIC PROCESS | 84 | -0.27 | -1.00 | 0.491 | 0.788 | 1.000 | 27362 | tags=56%, list=50%, signal=112% | |
2647 | POSITIVE REGULATION OF ACTIVIN RECEPTOR SIGNALING PATHWAY | 21 | -0.35 | -1.00 | 0.471 | 0.788 | 1.000 | 19772 | tags=52%, list=36%, signal=82% | |
2648 | POSITIVE REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 38 | -0.29 | -1.00 | 0.485 | 0.788 | 1.000 | 24473 | tags=53%, list=45%, signal=95% | |
2649 | POSITIVE REGULATION OF ATP METABOLIC PROCESS | 38 | -0.29 | -1.00 | 0.485 | 0.788 | 1.000 | 24473 | tags=53%, list=45%, signal=95% | |
2650 | POSITIVE REGULATION OF INTERLEUKIN-17 PRODUCTION | 17 | -0.39 | -1.00 | 0.472 | 0.788 | 1.000 | 31167 | tags=82%, list=57%, signal=191% | |
2651 | HEART TRABECULA MORPHOGENESIS | 29 | -0.30 | -1.00 | 0.468 | 0.788 | 1.000 | 7605 | tags=28%, list=14%, signal=32% | |
2652 | POLYNUCLEOTIDE DEPHOSPHORYLATION | 9 | -0.43 | -1.00 | 0.512 | 0.789 | 1.000 | 26361 | tags=78%, list=48%, signal=150% | |
2653 | CARDIAC EPITHELIAL TO MESENCHYMAL TRANSITION | 31 | -0.31 | -1.00 | 0.481 | 0.789 | 1.000 | 25051 | tags=55%, list=46%, signal=101% | |
2654 | REGULATION OF SEQUESTERING OF TRIGLYCERIDE | 37 | -0.31 | -1.00 | 0.498 | 0.789 | 1.000 | 32127 | tags=76%, list=59%, signal=183% | |
2655 | REGULATION OF INTERLEUKIN-6 PRODUCTION | 121 | -0.30 | -1.00 | 0.526 | 0.789 | 1.000 | 21556 | tags=49%, list=39%, signal=80% | |
2656 | V(D)J RECOMBINATION | 30 | -0.28 | -0.99 | 0.475 | 0.789 | 1.000 | 25567 | tags=53%, list=47%, signal=100% | |
2657 | PROTEIN FOLDING IN ENDOPLASMIC RETICULUM | 24 | -0.33 | -0.99 | 0.486 | 0.790 | 1.000 | 18436 | tags=46%, list=34%, signal=69% | |
2658 | REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 89 | -0.27 | -0.99 | 0.476 | 0.791 | 1.000 | 7829 | tags=22%, list=14%, signal=26% | |
2659 | MIRNA METABOLIC PROCESS | 9 | -0.41 | -0.99 | 0.490 | 0.791 | 1.000 | 29795 | tags=89%, list=54%, signal=195% | |
2660 | DESMOSOME ORGANIZATION | 16 | -0.37 | -0.99 | 0.485 | 0.791 | 1.000 | 22625 | tags=56%, list=41%, signal=96% | |
2661 | ACTIVIN RECEPTOR SIGNALING PATHWAY | 47 | -0.29 | -0.99 | 0.476 | 0.791 | 1.000 | 22260 | tags=51%, list=41%, signal=86% | |
2662 | NEGATIVE REGULATION OF ACTIN FILAMENT BUNDLE ASSEMBLY | 44 | -0.27 | -0.99 | 0.466 | 0.791 | 1.000 | 30488 | tags=64%, list=56%, signal=144% | |
2663 | REGULATION OF GROWTH | 740 | -0.23 | -0.99 | 0.530 | 0.791 | 1.000 | 28737 | tags=55%, list=53%, signal=114% | |
2664 | LOCOMOTORY BEHAVIOR | 85 | -0.25 | -0.99 | 0.490 | 0.791 | 1.000 | 19985 | tags=42%, list=37%, signal=67% | |
2665 | SEQUESTERING OF METAL ION | 15 | -0.39 | -0.99 | 0.490 | 0.791 | 1.000 | 19515 | tags=53%, list=36%, signal=83% | |
2666 | REGULATION OF MITOTIC SPINDLE ORGANIZATION | 31 | -0.34 | -0.99 | 0.495 | 0.792 | 1.000 | 25722 | tags=68%, list=47%, signal=128% | |
2667 | NEGATIVE REGULATION OF ORGAN GROWTH | 37 | -0.30 | -0.99 | 0.465 | 0.792 | 1.000 | 18246 | tags=43%, list=33%, signal=65% | |
2668 | DNA CONFORMATION CHANGE | 355 | -0.25 | -0.99 | 0.535 | 0.792 | 1.000 | 21253 | tags=45%, list=39%, signal=73% | |
2669 | STEM CELL PROLIFERATION | 96 | -0.26 | -0.99 | 0.480 | 0.793 | 1.000 | 32921 | tags=68%, list=60%, signal=170% | |
2670 | REGULATION OF CELLULAR COMPONENT SIZE | 375 | -0.24 | -0.99 | 0.523 | 0.793 | 1.000 | 19452 | tags=41%, list=36%, signal=63% | |
2671 | MITOCHONDRIAL FISSION | 38 | -0.32 | -0.99 | 0.509 | 0.793 | 1.000 | 21893 | tags=53%, list=40%, signal=88% | |
2672 | ACTIN FILAMENT-BASED PROCESS | 787 | -0.23 | -0.99 | 0.490 | 0.793 | 1.000 | 19032 | tags=39%, list=35%, signal=59% | |
2673 | AMINO-ACID BETAINE BIOSYNTHETIC PROCESS | 10 | -0.40 | -0.99 | 0.476 | 0.793 | 1.000 | 29335 | tags=80%, list=54%, signal=173% | |
2674 | CARNITINE BIOSYNTHETIC PROCESS | 10 | -0.40 | -0.99 | 0.476 | 0.793 | 1.000 | 29335 | tags=80%, list=54%, signal=173% | |
2675 | POSITIVE REGULATION OF ADAPTIVE IMMUNE RESPONSE | 99 | -0.27 | -0.99 | 0.496 | 0.793 | 1.000 | 17837 | tags=40%, list=33%, signal=60% | |
2676 | POSITIVE REGULATION OF DEFENSE RESPONSE TO VIRUS BY HOST | 242 | -0.25 | -0.99 | 0.494 | 0.793 | 1.000 | 24264 | tags=50%, list=44%, signal=90% | |
2677 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO GOLGI | 19 | -0.33 | -0.99 | 0.481 | 0.793 | 1.000 | 28664 | tags=68%, list=52%, signal=144% | |
2678 | RESPONSE TO TOXIC SUBSTANCE | 207 | -0.25 | -0.99 | 0.498 | 0.793 | 1.000 | 21309 | tags=44%, list=39%, signal=73% | |
2679 | CARNITINE SHUTTLE | 30 | -0.33 | -0.99 | 0.517 | 0.793 | 1.000 | 24104 | tags=63%, list=44%, signal=113% | |
2680 | FATTY ACID TRANSMEMBRANE TRANSPORT | 30 | -0.33 | -0.99 | 0.517 | 0.793 | 1.000 | 24104 | tags=63%, list=44%, signal=113% | |
2681 | REGULATION OF INTERLEUKIN-1 BETA PRODUCTION | 54 | -0.29 | -0.99 | 0.510 | 0.793 | 1.000 | 15325 | tags=37%, list=28%, signal=51% | |
2682 | REGULATION OF MICROTUBULE CYTOSKELETON ORGANIZATION | 236 | -0.26 | -0.99 | 0.506 | 0.793 | 1.000 | 18914 | tags=43%, list=35%, signal=65% | |
2683 | CELLULAR RESPONSE TO INTERFERON-GAMMA | 276 | -0.26 | -0.99 | 0.475 | 0.792 | 1.000 | 26977 | tags=58%, list=49%, signal=114% | |
2684 | POSITIVE REGULATION OF MRNA METABOLIC PROCESS | 90 | -0.26 | -0.99 | 0.482 | 0.792 | 1.000 | 29768 | tags=66%, list=54%, signal=144% | |
2685 | INNER EAR DEVELOPMENT | 91 | -0.26 | -0.99 | 0.483 | 0.793 | 1.000 | 29991 | tags=58%, list=55%, signal=129% | |
2686 | MULTIVESICULAR BODY SORTING PATHWAY | 27 | -0.36 | -0.99 | 0.502 | 0.793 | 1.000 | 30131 | tags=85%, list=55%, signal=190% | |
2687 | REGULATION OF IMMUNE EFFECTOR PROCESS | 712 | -0.24 | -0.99 | 0.534 | 0.793 | 1.000 | 21574 | tags=43%, list=39%, signal=71% | |
2688 | HISTONE H3-K36 METHYLATION | 18 | -0.35 | -0.99 | 0.479 | 0.795 | 1.000 | 4277 | tags=28%, list=8%, signal=30% | |
2689 | NEGATIVE REGULATION OF REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 17 | -0.35 | -0.99 | 0.489 | 0.795 | 1.000 | 11579 | tags=35%, list=21%, signal=45% | |
2690 | NEGATIVE REGULATION OF RHO PROTEIN SIGNAL TRANSDUCTION | 29 | -0.30 | -0.99 | 0.484 | 0.795 | 1.000 | 31430 | tags=69%, list=57%, signal=162% | |
2691 | REGULATION OF STORE-OPERATED CALCIUM CHANNEL ACTIVITY | 19 | -0.37 | -0.99 | 0.475 | 0.795 | 1.000 | 22210 | tags=63%, list=41%, signal=106% | |
2692 | POSITIVE REGULATION OF NEUROLOGICAL SYSTEM PROCESS | 17 | -0.34 | -0.99 | 0.516 | 0.795 | 1.000 | 21709 | tags=53%, list=40%, signal=88% | |
2693 | CHROMATIN ASSEMBLY | 167 | -0.27 | -0.99 | 0.530 | 0.795 | 1.000 | 22799 | tags=49%, list=42%, signal=84% | |
2694 | ANATOMICAL STRUCTURE HOMEOSTASIS | 395 | -0.24 | -0.99 | 0.528 | 0.795 | 1.000 | 20343 | tags=41%, list=37%, signal=65% | |
2695 | PROTEIN TARGETING TO LYSOSOME | 40 | -0.32 | -0.99 | 0.533 | 0.795 | 1.000 | 13729 | tags=40%, list=25%, signal=53% | |
2696 | POSITIVE REGULATION OF OXIDOREDUCTASE ACTIVITY | 79 | -0.28 | -0.99 | 0.494 | 0.795 | 1.000 | 16984 | tags=38%, list=31%, signal=55% | |
2697 | CORPUS CALLOSUM DEVELOPMENT | 17 | -0.35 | -0.99 | 0.473 | 0.795 | 1.000 | 29044 | tags=71%, list=53%, signal=151% | |
2698 | REGULATION OF PLASMA MEMBRANE ORGANIZATION | 178 | -0.26 | -0.99 | 0.533 | 0.795 | 1.000 | 30495 | tags=63%, list=56%, signal=142% | |
2699 | REGULATION OF TRIGLYCERIDE METABOLIC PROCESS | 59 | -0.27 | -0.99 | 0.472 | 0.795 | 1.000 | 16447 | tags=36%, list=30%, signal=51% | |
2700 | NEGATIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 357 | -0.24 | -0.99 | 0.524 | 0.796 | 1.000 | 23502 | tags=46%, list=43%, signal=81% | |
2701 | ACTIVATION OF PROTEIN KINASE ACTIVITY | 964 | -0.22 | -0.99 | 0.544 | 0.796 | 1.000 | 21892 | tags=42%, list=40%, signal=69% | |
2702 | NEGATIVE REGULATION OF PHOSPHORYLATION | 694 | -0.25 | -0.99 | 0.575 | 0.796 | 1.000 | 25937 | tags=53%, list=47%, signal=100% | |
2703 | CELLULAR SENESCENCE | 80 | -0.26 | -0.99 | 0.502 | 0.796 | 1.000 | 24508 | tags=49%, list=45%, signal=88% | |
2704 | SECONDARY ALCOHOL METABOLIC PROCESS | 119 | -0.25 | -0.99 | 0.490 | 0.797 | 1.000 | 22187 | tags=47%, list=41%, signal=79% | |
2705 | C4-DICARBOXYLATE TRANSPORT | 18 | -0.31 | -0.99 | 0.533 | 0.797 | 1.000 | 6391 | tags=28%, list=12%, signal=31% | |
2706 | REGULATION OF WOUND HEALING, SPREADING OF EPIDERMAL CELLS | 26 | -0.30 | -0.99 | 0.487 | 0.797 | 1.000 | 18901 | tags=42%, list=35%, signal=65% | |
2707 | HISTONE LYSINE DEMETHYLATION | 43 | -0.30 | -0.99 | 0.481 | 0.796 | 1.000 | 30398 | tags=70%, list=56%, signal=157% | |
2708 | NEGATIVE REGULATION OF NEURON DEATH | 143 | -0.26 | -0.99 | 0.547 | 0.797 | 1.000 | 22028 | tags=46%, list=40%, signal=77% | |
2709 | POSITIVE REGULATION OF RESPONSE TO DNA DAMAGE STIMULUS | 131 | -0.26 | -0.99 | 0.505 | 0.797 | 1.000 | 25044 | tags=53%, list=46%, signal=97% | |
2710 | DNA LIGATION INVOLVED IN DNA REPAIR | 17 | -0.35 | -0.99 | 0.519 | 0.797 | 1.000 | 27915 | tags=65%, list=51%, signal=132% | |
2711 | CELLULAR BIOGENIC AMINE BIOSYNTHETIC PROCESS | 24 | -0.31 | -0.98 | 0.468 | 0.798 | 1.000 | 5870 | tags=21%, list=11%, signal=23% | |
2712 | REGULATION OF T CELL MEDIATED CYTOTOXICITY | 44 | -0.31 | -0.98 | 0.438 | 0.798 | 1.000 | 17332 | tags=41%, list=32%, signal=60% | |
2713 | PHOTOPERIODISM | 52 | -0.27 | -0.98 | 0.490 | 0.798 | 1.000 | 22427 | tags=50%, list=41%, signal=85% | |
2714 | KERATAN SULFATE CATABOLIC PROCESS | 25 | -0.32 | -0.98 | 0.495 | 0.799 | 1.000 | 9046 | tags=32%, list=17%, signal=38% | |
2715 | REGULATION OF SHORT-TERM NEURONAL SYNAPTIC PLASTICITY | 20 | -0.31 | -0.98 | 0.478 | 0.799 | 1.000 | 17082 | tags=35%, list=31%, signal=51% | |
2716 | HEPATICOBILIARY SYSTEM DEVELOPMENT | 61 | -0.29 | -0.98 | 0.489 | 0.799 | 1.000 | 22928 | tags=52%, list=42%, signal=90% | |
2717 | POSITIVE REGULATION OF INTERLEUKIN-6 PRODUCTION | 65 | -0.32 | -0.98 | 0.514 | 0.799 | 1.000 | 18446 | tags=46%, list=34%, signal=70% | |
2718 | LYSOSOME LOCALIZATION | 34 | -0.32 | -0.98 | 0.521 | 0.799 | 1.000 | 19071 | tags=47%, list=35%, signal=72% | |
2719 | REGULATION OF CELL SHAPE | 200 | -0.26 | -0.98 | 0.561 | 0.799 | 1.000 | 26637 | tags=56%, list=49%, signal=108% | |
2720 | REGULATION OF VASCULOGENESIS | 28 | -0.31 | -0.98 | 0.528 | 0.799 | 1.000 | 25051 | tags=61%, list=46%, signal=112% | |
2721 | NEGATIVE REGULATION OF PATHWAY-RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 27 | -0.29 | -0.98 | 0.523 | 0.799 | 1.000 | 33897 | tags=67%, list=62%, signal=175% | |
2722 | RESPONSE TO COLD | 36 | -0.31 | -0.98 | 0.533 | 0.799 | 1.000 | 31492 | tags=78%, list=58%, signal=183% | |
2723 | NUCLEOSIDE TRIPHOSPHATE CATABOLIC PROCESS | 19 | -0.35 | -0.98 | 0.484 | 0.799 | 1.000 | 16120 | tags=47%, list=29%, signal=67% | |
2724 | POSITIVE REGULATION OF PATHWAY-RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 78 | -0.27 | -0.98 | 0.524 | 0.799 | 1.000 | 22412 | tags=47%, list=41%, signal=80% | |
2725 | BILE ACID BIOSYNTHETIC PROCESS | 32 | -0.31 | -0.98 | 0.499 | 0.799 | 1.000 | 19320 | tags=47%, list=35%, signal=72% | |
2726 | NEGATIVE REGULATION OF CELL CYCLE G2/M PHASE TRANSITION | 60 | -0.28 | -0.98 | 0.486 | 0.801 | 1.000 | 14139 | tags=33%, list=26%, signal=45% | |
2727 | LEUKOCYTE MEDIATED CYTOTOXICITY | 28 | -0.32 | -0.98 | 0.533 | 0.801 | 1.000 | 27978 | tags=68%, list=51%, signal=139% | |
2728 | NEGATIVE REGULATION OF CAMP-MEDIATED SIGNALING | 15 | -0.37 | -0.98 | 0.509 | 0.801 | 1.000 | 16185 | tags=47%, list=30%, signal=66% | |
2729 | POSITIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 95 | -0.27 | -0.98 | 0.512 | 0.801 | 1.000 | 22427 | tags=48%, list=41%, signal=82% | |
2730 | NEGATIVE REGULATION OF CELL PROLIFERATION | 1020 | -0.23 | -0.98 | 0.545 | 0.801 | 1.000 | 24899 | tags=49%, list=46%, signal=88% | |
2731 | POSITIVE REGULATION OF ACTIN NUCLEATION | 22 | -0.33 | -0.98 | 0.499 | 0.801 | 1.000 | 22819 | tags=59%, list=42%, signal=101% | |
2732 | REGULATION OF GOLGI TO PLASMA MEMBRANE PROTEIN TRANSPORT | 12 | -0.36 | -0.98 | 0.465 | 0.801 | 1.000 | 29292 | tags=75%, list=54%, signal=162% | |
2733 | NEGATIVE REGULATION OF DENDRITE MORPHOGENESIS | 24 | -0.34 | -0.98 | 0.505 | 0.801 | 1.000 | 26579 | tags=71%, list=49%, signal=138% | |
2734 | NLS-BEARING PROTEIN IMPORT INTO NUCLEUS | 61 | -0.31 | -0.98 | 0.515 | 0.801 | 1.000 | 27143 | tags=66%, list=50%, signal=130% | |
2735 | CELLULAR PIGMENTATION | 64 | -0.30 | -0.98 | 0.529 | 0.800 | 1.000 | 31793 | tags=75%, list=58%, signal=179% | |
2736 | SOMATIC RECOMBINATION OF IMMUNOGLOBULIN GENES INVOLVED IN IMMUNE RESPONSE | 26 | -0.33 | -0.98 | 0.497 | 0.802 | 1.000 | 17597 | tags=46%, list=32%, signal=68% | |
2737 | SOMATIC DIVERSIFICATION OF IMMUNOGLOBULINS INVOLVED IN IMMUNE RESPONSE | 26 | -0.33 | -0.98 | 0.497 | 0.801 | 1.000 | 17597 | tags=46%, list=32%, signal=68% | |
2738 | ISOTYPE SWITCHING | 26 | -0.33 | -0.98 | 0.497 | 0.801 | 1.000 | 17597 | tags=46%, list=32%, signal=68% | |
2739 | REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 514 | -0.24 | -0.98 | 0.564 | 0.801 | 1.000 | 29273 | tags=58%, list=54%, signal=124% | |
2740 | ASYMMETRIC STEM CELL DIVISION | 12 | -0.39 | -0.98 | 0.501 | 0.801 | 1.000 | 12051 | tags=42%, list=22%, signal=53% | |
2741 | NEGATIVE REGULATION OF TRANSLATIONAL INITIATION | 40 | -0.33 | -0.98 | 0.543 | 0.801 | 1.000 | 9633 | tags=35%, list=18%, signal=42% | |
2742 | VIRAL MRNA EXPORT FROM HOST CELL NUCLEUS | 14 | -0.38 | -0.98 | 0.516 | 0.801 | 1.000 | 31739 | tags=86%, list=58%, signal=204% | |
2743 | CEREBRAL CORTEX RADIALLY ORIENTED CELL MIGRATION | 24 | -0.33 | -0.98 | 0.498 | 0.801 | 1.000 | 11496 | tags=33%, list=21%, signal=42% | |
2744 | MEMBRANE LIPID BIOSYNTHETIC PROCESS | 188 | -0.27 | -0.98 | 0.558 | 0.802 | 1.000 | 31345 | tags=69%, list=57%, signal=161% | |
2745 | POSITIVE REGULATION OF MAP KINASE ACTIVITY | 345 | -0.24 | -0.98 | 0.492 | 0.802 | 1.000 | 18217 | tags=36%, list=33%, signal=54% | |
2746 | REGULATION OF PROTEIN EXPORT FROM NUCLEUS | 59 | -0.30 | -0.98 | 0.525 | 0.801 | 1.000 | 28032 | tags=68%, list=51%, signal=139% | |
2747 | REGULATION OF DNA BINDING | 142 | -0.25 | -0.98 | 0.557 | 0.802 | 1.000 | 20719 | tags=43%, list=38%, signal=69% | |
2748 | POSITIVE REGULATION OF PROTEIN SECRETION | 266 | -0.24 | -0.98 | 0.537 | 0.802 | 1.000 | 22892 | tags=46%, list=42%, signal=79% | |
2749 | PROTEIN LOCALIZATION TO MICROTUBULE CYTOSKELETON | 49 | -0.32 | -0.98 | 0.547 | 0.803 | 1.000 | 29005 | tags=73%, list=53%, signal=156% | |
2750 | POSITIVE REGULATION OF MYELOID LEUKOCYTE DIFFERENTIATION | 69 | -0.26 | -0.98 | 0.524 | 0.803 | 1.000 | 27116 | tags=48%, list=50%, signal=95% | |
2751 | REGULATION OF PATHWAY-RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 105 | -0.26 | -0.98 | 0.548 | 0.803 | 1.000 | 34080 | tags=70%, list=62%, signal=184% | |
2752 | POSITIVE REGULATION OF ALPHA-BETA T CELL ACTIVATION | 64 | -0.29 | -0.98 | 0.488 | 0.803 | 1.000 | 25520 | tags=53%, list=47%, signal=100% | |
2753 | POSITIVE REGULATION OF MRNA PROCESSING | 64 | -0.28 | -0.98 | 0.509 | 0.803 | 1.000 | 22173 | tags=52%, list=41%, signal=87% | |
2754 | NEGATIVE REGULATION OF VIRAL ENTRY INTO HOST CELL | 29 | -0.33 | -0.98 | 0.538 | 0.803 | 1.000 | 23491 | tags=59%, list=43%, signal=103% | |
2755 | REGULATION OF TOLL-LIKE RECEPTOR 2 SIGNALING PATHWAY | 12 | -0.40 | -0.98 | 0.493 | 0.803 | 1.000 | 32672 | tags=100%, list=60%, signal=248% | |
2756 | REGULATION OF GLIAL CELL PROLIFERATION | 24 | -0.31 | -0.98 | 0.513 | 0.803 | 1.000 | 6207 | tags=25%, list=11%, signal=28% | |
2757 | PROTEIN DESTABILIZATION | 67 | -0.28 | -0.98 | 0.507 | 0.804 | 1.000 | 30833 | tags=67%, list=56%, signal=154% | |
2758 | MONOCYTE DIFFERENTIATION | 14 | -0.35 | -0.98 | 0.481 | 0.804 | 1.000 | 11376 | tags=36%, list=21%, signal=45% | |
2759 | TELOMERE MAINTENANCE VIA RECOMBINATION | 50 | -0.31 | -0.98 | 0.537 | 0.804 | 1.000 | 20280 | tags=54%, list=37%, signal=86% | |
2760 | NUCLEAR RNA SURVEILLANCE | 10 | -0.40 | -0.98 | 0.502 | 0.804 | 1.000 | 29604 | tags=90%, list=54%, signal=196% | |
2761 | NUCLEAR MRNA SURVEILLANCE | 10 | -0.40 | -0.98 | 0.502 | 0.804 | 1.000 | 29604 | tags=90%, list=54%, signal=196% | |
2762 | UNSATURATED FATTY ACID METABOLIC PROCESS | 167 | -0.25 | -0.98 | 0.545 | 0.804 | 1.000 | 28804 | tags=61%, list=53%, signal=129% | |
2763 | NEGATIVE REGULATION OF POTASSIUM ION TRANSMEMBRANE TRANSPORT | 39 | -0.27 | -0.98 | 0.492 | 0.805 | 1.000 | 25853 | tags=54%, list=47%, signal=102% | |
2764 | DNA SYNTHESIS INVOLVED IN DNA REPAIR | 19 | -0.35 | -0.98 | 0.513 | 0.805 | 1.000 | 27751 | tags=74%, list=51%, signal=150% | |
2765 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 40 | -0.32 | -0.98 | 0.520 | 0.805 | 1.000 | 7049 | tags=23%, list=13%, signal=26% | |
2766 | PALATE DEVELOPMENT | 78 | -0.25 | -0.98 | 0.517 | 0.805 | 1.000 | 34790 | tags=69%, list=64%, signal=190% | |
2767 | OPTIC CUP MORPHOGENESIS INVOLVED IN CAMERA-TYPE EYE DEVELOPMENT | 14 | -0.35 | -0.98 | 0.490 | 0.804 | 1.000 | 19696 | tags=50%, list=36%, signal=78% | |
2768 | INTERACTION WITH SYMBIONT | 108 | -0.26 | -0.97 | 0.526 | 0.806 | 1.000 | 20339 | tags=45%, list=37%, signal=72% | |
2769 | REGULATION OF INTERFERON-ALPHA PRODUCTION | 35 | -0.33 | -0.97 | 0.529 | 0.806 | 1.000 | 17597 | tags=46%, list=32%, signal=67% | |
2770 | NEURON PROJECTION REGENERATION | 10 | -0.39 | -0.97 | 0.491 | 0.805 | 1.000 | 27195 | tags=80%, list=50%, signal=159% | |
2771 | AXON REGENERATION | 10 | -0.39 | -0.97 | 0.491 | 0.805 | 1.000 | 27195 | tags=80%, list=50%, signal=159% | |
2772 | AMMONIUM TRANSMEMBRANE TRANSPORT | 61 | -0.27 | -0.97 | 0.501 | 0.805 | 1.000 | 22600 | tags=49%, list=41%, signal=84% | |
2773 | REGULATION OF RESPONSE TO CYTOKINE STIMULUS | 262 | -0.25 | -0.97 | 0.564 | 0.806 | 1.000 | 17480 | tags=37%, list=32%, signal=54% | |
2774 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER INVOLVED IN HEART DEVELOPMENT | 10 | -0.40 | -0.97 | 0.499 | 0.806 | 1.000 | 16716 | tags=50%, list=31%, signal=72% | |
2775 | CELLULAR RESPONSE TO ESTROGEN STIMULUS | 60 | -0.26 | -0.97 | 0.531 | 0.808 | 1.000 | 10442 | tags=27%, list=19%, signal=33% | |
2776 | ORGANIC HYDROXY COMPOUND TRANSPORT | 232 | -0.24 | -0.97 | 0.537 | 0.807 | 1.000 | 22600 | tags=44%, list=41%, signal=75% | |
2777 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA2 PRODUCTION | 18 | -0.35 | -0.97 | 0.523 | 0.807 | 1.000 | 18672 | tags=44%, list=34%, signal=67% | |
2778 | REGULATION OF GENE SILENCING | 60 | -0.27 | -0.97 | 0.536 | 0.807 | 1.000 | 16778 | tags=35%, list=31%, signal=50% | |
2779 | CYSTEINE METABOLIC PROCESS | 20 | -0.33 | -0.97 | 0.506 | 0.807 | 1.000 | 24741 | tags=60%, list=45%, signal=110% | |
2780 | EPITHELIAL CELL DIFFERENTIATION | 534 | -0.23 | -0.97 | 0.544 | 0.808 | 1.000 | 28323 | tags=55%, list=52%, signal=113% | |
2781 | POSITIVE REGULATION OF SYNAPTIC TRANSMISSION | 113 | -0.23 | -0.97 | 0.494 | 0.808 | 1.000 | 18246 | tags=34%, list=33%, signal=50% | |
2782 | POSITIVE REGULATION OF VIRAL GENOME REPLICATION | 78 | -0.28 | -0.97 | 0.531 | 0.808 | 1.000 | 21191 | tags=47%, list=39%, signal=77% | |
2783 | MITOCHONDRIAL DNA METABOLIC PROCESS | 7 | -0.43 | -0.97 | 0.536 | 0.808 | 1.000 | 15714 | tags=57%, list=29%, signal=80% | |
2784 | REGULATION OF CHROMATIN BINDING | 8 | -0.39 | -0.97 | 0.495 | 0.808 | 1.000 | 28884 | tags=75%, list=53%, signal=159% | |
2785 | POSITIVE REGULATION OF INTERLEUKIN-5 PRODUCTION | 17 | -0.35 | -0.97 | 0.511 | 0.809 | 1.000 | 14123 | tags=35%, list=26%, signal=48% | |
2786 | POSITIVE REGULATION OF POTASSIUM ION TRANSMEMBRANE TRANSPORT | 40 | -0.26 | -0.97 | 0.494 | 0.809 | 1.000 | 16903 | tags=35%, list=31%, signal=51% | |
2787 | NATURAL KILLER CELL ACTIVATION | 21 | -0.34 | -0.97 | 0.503 | 0.808 | 1.000 | 13668 | tags=38%, list=25%, signal=51% | |
2788 | POSITIVE REGULATION OF STRESS FIBER ASSEMBLY | 79 | -0.28 | -0.97 | 0.493 | 0.809 | 1.000 | 33766 | tags=78%, list=62%, signal=205% | |
2789 | POSITIVE REGULATION OF ASTROCYTE DIFFERENTIATION | 15 | -0.38 | -0.97 | 0.503 | 0.809 | 1.000 | 27471 | tags=67%, list=50%, signal=134% | |
2790 | GOLGI LOCALIZATION | 23 | -0.35 | -0.97 | 0.551 | 0.809 | 1.000 | 29005 | tags=78%, list=53%, signal=167% | |
2791 | SKELETAL MUSCLE ORGAN DEVELOPMENT | 82 | -0.25 | -0.97 | 0.501 | 0.809 | 1.000 | 21818 | tags=45%, list=40%, signal=75% | |
2792 | CELLULAR RESPONSE TO MURAMYL DIPEPTIDE | 13 | -0.37 | -0.97 | 0.537 | 0.809 | 1.000 | 22724 | tags=62%, list=42%, signal=105% | |
2793 | CHROMATIN-MEDIATED MAINTENANCE OF TRANSCRIPTION | 17 | -0.35 | -0.97 | 0.488 | 0.810 | 1.000 | 16930 | tags=47%, list=31%, signal=68% | |
2794 | RESPIRATORY TUBE DEVELOPMENT | 100 | -0.25 | -0.97 | 0.533 | 0.810 | 1.000 | 17992 | tags=38%, list=33%, signal=57% | |
2795 | NUCLEAR IMPORT | 184 | -0.27 | -0.97 | 0.565 | 0.810 | 1.000 | 27143 | tags=59%, list=50%, signal=117% | |
2796 | NITROGEN COMPOUND TRANSPORT | 666 | -0.23 | -0.97 | 0.569 | 0.810 | 1.000 | 22668 | tags=45%, list=41%, signal=76% | |
2797 | REGULATION OF MICROTUBULE POLYMERIZATION | 56 | -0.27 | -0.97 | 0.536 | 0.809 | 1.000 | 18901 | tags=41%, list=35%, signal=63% | |
2798 | G2 DNA DAMAGE CHECKPOINT | 90 | -0.28 | -0.97 | 0.545 | 0.809 | 1.000 | 15421 | tags=38%, list=28%, signal=53% | |
2799 | POSITIVE REGULATION OF CALCINEURIN-NFAT SIGNALING CASCADE | 20 | -0.34 | -0.97 | 0.524 | 0.809 | 1.000 | 22671 | tags=55%, list=41%, signal=94% | |
2800 | HISTONE MRNA CATABOLIC PROCESS | 31 | -0.32 | -0.97 | 0.499 | 0.809 | 1.000 | 30784 | tags=74%, list=56%, signal=170% | |
2801 | NEGATIVE REGULATION OF ANDROGEN RECEPTOR SIGNALING PATHWAY | 48 | -0.28 | -0.97 | 0.545 | 0.809 | 1.000 | 19607 | tags=46%, list=36%, signal=71% | |
2802 | CELL-CELL JUNCTION ORGANIZATION | 339 | -0.24 | -0.97 | 0.548 | 0.808 | 1.000 | 20835 | tags=42%, list=38%, signal=67% | |
2803 | TYPE 2 IMMUNE RESPONSE | 11 | -0.37 | -0.97 | 0.531 | 0.808 | 1.000 | 15621 | tags=45%, list=29%, signal=64% | |
2804 | NEGATIVE REGULATION OF RESPONSE TO FOOD | 22 | -0.30 | -0.97 | 0.505 | 0.809 | 1.000 | 31909 | tags=77%, list=58%, signal=186% | |
2805 | NEGATIVE REGULATION OF APPETITE | 22 | -0.30 | -0.97 | 0.505 | 0.808 | 1.000 | 31909 | tags=77%, list=58%, signal=186% | |
2806 | POSITIVE REGULATION OF BRANCHING INVOLVED IN URETERIC BUD MORPHOGENESIS | 28 | -0.29 | -0.97 | 0.508 | 0.808 | 1.000 | 17093 | tags=36%, list=31%, signal=52% | |
2807 | MEMBRANE BIOGENESIS | 85 | -0.26 | -0.97 | 0.507 | 0.808 | 1.000 | 21605 | tags=46%, list=40%, signal=76% | |
2808 | NEGATIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 145 | -0.26 | -0.97 | 0.602 | 0.808 | 1.000 | 29323 | tags=63%, list=54%, signal=135% | |
2809 | ESTABLISHMENT OR MAINTENANCE OF EPITHELIAL CELL APICAL/BASAL POLARITY | 16 | -0.33 | -0.97 | 0.475 | 0.808 | 1.000 | 5639 | tags=19%, list=10%, signal=21% | |
2810 | POSITIVE REGULATION OF FATTY ACID METABOLIC PROCESS | 46 | -0.28 | -0.97 | 0.514 | 0.808 | 1.000 | 11373 | tags=28%, list=21%, signal=36% | |
2811 | REGULATION OF ODONTOGENESIS | 20 | -0.33 | -0.97 | 0.516 | 0.807 | 1.000 | 24638 | tags=55%, list=45%, signal=100% | |
2812 | REGULATION OF LIPID KINASE ACTIVITY | 74 | -0.24 | -0.97 | 0.518 | 0.807 | 1.000 | 22664 | tags=42%, list=41%, signal=71% | |
2813 | REGULATION OF RECEPTOR BIOSYNTHETIC PROCESS | 47 | -0.28 | -0.97 | 0.564 | 0.808 | 1.000 | 31774 | tags=72%, list=58%, signal=173% | |
2814 | GROWTH | 301 | -0.23 | -0.97 | 0.601 | 0.807 | 1.000 | 17788 | tags=37%, list=33%, signal=54% | |
2815 | REGULATION OF PROTEIN COMPLEX STABILITY | 14 | -0.36 | -0.97 | 0.531 | 0.808 | 1.000 | 12047 | tags=43%, list=22%, signal=55% | |
2816 | STEROID BIOSYNTHETIC PROCESS | 156 | -0.24 | -0.97 | 0.524 | 0.808 | 1.000 | 23957 | tags=49%, list=44%, signal=86% | |
2817 | MAMMARY GLAND MORPHOGENESIS | 20 | -0.35 | -0.97 | 0.522 | 0.808 | 1.000 | 15718 | tags=45%, list=29%, signal=63% | |
2818 | NEGATIVE REGULATION OF OXIDATIVE STRESS-INDUCED NEURON DEATH | 16 | -0.35 | -0.97 | 0.538 | 0.808 | 1.000 | 6843 | tags=31%, list=13%, signal=36% | |
2819 | POLYPRENOL METABOLIC PROCESS | 10 | -0.42 | -0.97 | 0.507 | 0.808 | 1.000 | 20477 | tags=70%, list=37%, signal=112% | |
2820 | HAIR FOLLICLE DEVELOPMENT | 52 | -0.27 | -0.97 | 0.523 | 0.809 | 1.000 | 29991 | tags=62%, list=55%, signal=136% | |
2821 | PHOSPHATIDYLINOSITOL ACYL-CHAIN REMODELING | 24 | -0.30 | -0.97 | 0.516 | 0.809 | 1.000 | 30564 | tags=71%, list=56%, signal=161% | |
2822 | METHIONINE BIOSYNTHETIC PROCESS | 24 | -0.33 | -0.97 | 0.511 | 0.810 | 1.000 | 29186 | tags=75%, list=53%, signal=161% | |
2823 | PYRIMIDINE-CONTAINING COMPOUND TRANSMEMBRANE TRANSPORT | 16 | -0.36 | -0.97 | 0.515 | 0.810 | 1.000 | 16715 | tags=50%, list=31%, signal=72% | |
2824 | REGULATION OF NATURAL KILLER CELL MEDIATED IMMUNITY | 61 | -0.28 | -0.97 | 0.524 | 0.810 | 1.000 | 20653 | tags=46%, list=38%, signal=74% | |
2825 | GLOMERULAR EPITHELIUM DEVELOPMENT | 38 | -0.29 | -0.97 | 0.538 | 0.810 | 1.000 | 28190 | tags=61%, list=52%, signal=125% | |
2826 | POSITIVE REGULATION OF MESENCHYMAL CELL PROLIFERATION | 35 | -0.30 | -0.97 | 0.488 | 0.810 | 1.000 | 16824 | tags=40%, list=31%, signal=58% | |
2827 | PROTEIN IMPORT INTO NUCLEUS | 175 | -0.27 | -0.97 | 0.575 | 0.811 | 1.000 | 27143 | tags=59%, list=50%, signal=117% | |
2828 | PROTEIN TARGETING TO NUCLEUS | 175 | -0.27 | -0.97 | 0.575 | 0.810 | 1.000 | 27143 | tags=59%, list=50%, signal=117% | |
2829 | SINGLE-ORGANISM NUCLEAR IMPORT | 175 | -0.27 | -0.97 | 0.575 | 0.810 | 1.000 | 27143 | tags=59%, list=50%, signal=117% | |
2830 | REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 161 | -0.26 | -0.97 | 0.574 | 0.810 | 1.000 | 23904 | tags=50%, list=44%, signal=89% | |
2831 | REGULATION OF ALPHA-BETA T CELL ACTIVATION | 101 | -0.27 | -0.97 | 0.510 | 0.810 | 1.000 | 25520 | tags=50%, list=47%, signal=95% | |
2832 | REGULATION OF MRNA CATABOLIC PROCESS | 63 | -0.28 | -0.97 | 0.510 | 0.810 | 1.000 | 30368 | tags=70%, list=56%, signal=157% | |
2833 | REGULATION OF PLATELET AGGREGATION | 27 | -0.33 | -0.97 | 0.491 | 0.811 | 1.000 | 11512 | tags=33%, list=21%, signal=42% | |
2834 | REGULATION OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 157 | -0.25 | -0.96 | 0.569 | 0.811 | 1.000 | 30139 | tags=63%, list=55%, signal=140% | |
2835 | REGULATION OF PROTEIN LOCALIZATION TO CELL PERIPHERY | 157 | -0.25 | -0.96 | 0.569 | 0.811 | 1.000 | 30139 | tags=63%, list=55%, signal=140% | |
2836 | LATERAL VENTRICLE DEVELOPMENT | 16 | -0.36 | -0.96 | 0.519 | 0.811 | 1.000 | 22036 | tags=63%, list=40%, signal=105% | |
2837 | NEGATIVE REGULATION OF TOLL-LIKE RECEPTOR 4 SIGNALING PATHWAY | 15 | -0.36 | -0.96 | 0.535 | 0.811 | 1.000 | 32672 | tags=73%, list=60%, signal=182% | |
2838 | DEPHOSPHORYLATION | 435 | -0.25 | -0.96 | 0.559 | 0.811 | 1.000 | 23079 | tags=50%, list=42%, signal=86% | |
2839 | BINDING OF SPERM TO ZONA PELLUCIDA | 28 | -0.31 | -0.96 | 0.521 | 0.811 | 1.000 | 12887 | tags=32%, list=24%, signal=42% | |
2840 | REGULATION OF INTEGRIN ACTIVATION | 26 | -0.30 | -0.96 | 0.490 | 0.811 | 1.000 | 21318 | tags=46%, list=39%, signal=76% | |
2841 | POSITIVE REGULATION OF PEPTIDE SECRETION | 99 | -0.27 | -0.96 | 0.517 | 0.811 | 1.000 | 23125 | tags=51%, list=42%, signal=87% | |
2842 | POSITIVE REGULATION OF PEPTIDE HORMONE SECRETION | 99 | -0.27 | -0.96 | 0.517 | 0.811 | 1.000 | 23125 | tags=51%, list=42%, signal=87% | |
2843 | RESPONSE TO CARBOHYDRATE | 113 | -0.25 | -0.96 | 0.536 | 0.811 | 1.000 | 17426 | tags=38%, list=32%, signal=56% | |
2844 | ACUTE-PHASE RESPONSE | 28 | -0.34 | -0.96 | 0.529 | 0.811 | 1.000 | 18206 | tags=36%, list=33%, signal=54% | |
2845 | POSITIVE REGULATION OF RHO PROTEIN SIGNAL TRANSDUCTION | 30 | -0.32 | -0.96 | 0.498 | 0.811 | 1.000 | 15146 | tags=37%, list=28%, signal=51% | |
2846 | PROTEIN-LIPID COMPLEX SUBUNIT ORGANIZATION | 63 | -0.26 | -0.96 | 0.473 | 0.811 | 1.000 | 21720 | tags=44%, list=40%, signal=74% | |
2847 | NEGATIVE REGULATION OF T CELL APOPTOTIC PROCESS | 14 | -0.38 | -0.96 | 0.510 | 0.811 | 1.000 | 22721 | tags=57%, list=42%, signal=98% | |
2848 | TRNA METHYLATION | 18 | -0.36 | -0.96 | 0.511 | 0.811 | 1.000 | 33303 | tags=89%, list=61%, signal=227% | |
2849 | GLYCOLIPID CATABOLIC PROCESS | 15 | -0.35 | -0.96 | 0.526 | 0.811 | 1.000 | 27045 | tags=67%, list=49%, signal=132% | |
2850 | PHOSPHATIDYLINOSITOL-3-PHOSPHATE BIOSYNTHETIC PROCESS | 30 | -0.31 | -0.96 | 0.523 | 0.811 | 1.000 | 14171 | tags=37%, list=26%, signal=49% | |
2851 | POSITIVE REGULATION OF PROTEIN DEPOLYMERIZATION | 41 | -0.28 | -0.96 | 0.535 | 0.811 | 1.000 | 18826 | tags=44%, list=34%, signal=67% | |
2852 | REGULATION OF CHEMOKINE BIOSYNTHETIC PROCESS | 9 | -0.38 | -0.96 | 0.516 | 0.811 | 1.000 | 6573 | tags=33%, list=12%, signal=38% | |
2853 | MITOTIC SPINDLE ELONGATION | 9 | -0.39 | -0.96 | 0.534 | 0.810 | 1.000 | 30730 | tags=89%, list=56%, signal=203% | |
2854 | SPINDLE ELONGATION | 9 | -0.39 | -0.96 | 0.534 | 0.810 | 1.000 | 30730 | tags=89%, list=56%, signal=203% | |
2855 | REGULATION OF DIGESTIVE SYSTEM PROCESS | 16 | -0.34 | -0.96 | 0.504 | 0.810 | 1.000 | 19196 | tags=44%, list=35%, signal=67% | |
2856 | REGULATION OF INTERLEUKIN-8 SECRETION | 31 | -0.32 | -0.96 | 0.538 | 0.810 | 1.000 | 16328 | tags=42%, list=30%, signal=60% | |
2857 | REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 256 | -0.24 | -0.96 | 0.599 | 0.810 | 1.000 | 29286 | tags=57%, list=54%, signal=123% | |
2858 | POSITIVE REGULATION OF MRNA CATABOLIC PROCESS | 57 | -0.28 | -0.96 | 0.523 | 0.811 | 1.000 | 30368 | tags=70%, list=56%, signal=158% | |
2859 | REGULATION OF POLYSACCHARIDE METABOLIC PROCESS | 82 | -0.25 | -0.96 | 0.540 | 0.811 | 1.000 | 13561 | tags=30%, list=25%, signal=40% | |
2860 | I-KAPPAB KINASE/NF-KAPPAB SIGNALING | 99 | -0.28 | -0.96 | 0.544 | 0.811 | 1.000 | 13491 | tags=35%, list=25%, signal=47% | |
2861 | REGULATION OF PROTEIN SECRETION | 587 | -0.23 | -0.96 | 0.555 | 0.811 | 1.000 | 22664 | tags=43%, list=41%, signal=73% | |
2862 | NEGATIVE REGULATION OF PEPTIDYL-SERINE PHOSPHORYLATION | 35 | -0.31 | -0.96 | 0.580 | 0.812 | 1.000 | 28323 | tags=71%, list=52%, signal=148% | |
2863 | REGULATION OF ACTIN FILAMENT BUNDLE ASSEMBLY | 155 | -0.24 | -0.96 | 0.552 | 0.813 | 1.000 | 31995 | tags=66%, list=59%, signal=160% | |
2864 | NEGATIVE REGULATION OF SUBSTRATE ADHESION-DEPENDENT CELL SPREADING | 31 | -0.28 | -0.96 | 0.527 | 0.813 | 1.000 | 14116 | tags=32%, list=26%, signal=43% | |
2865 | REGULATION OF ANGIOTENSIN LEVELS IN BLOOD | 23 | -0.32 | -0.96 | 0.507 | 0.813 | 1.000 | 9404 | tags=26%, list=17%, signal=31% | |
2866 | REGULATION OF ANGIOTENSIN METABOLIC PROCESS | 23 | -0.32 | -0.96 | 0.507 | 0.812 | 1.000 | 9404 | tags=26%, list=17%, signal=31% | |
2867 | REGULATION OF TOLL-LIKE RECEPTOR 4 SIGNALING PATHWAY | 31 | -0.30 | -0.96 | 0.533 | 0.813 | 1.000 | 21357 | tags=45%, list=39%, signal=74% | |
2868 | REGULATION OF LEUKOCYTE MEDIATED IMMUNITY | 221 | -0.26 | -0.96 | 0.511 | 0.813 | 1.000 | 11234 | tags=27%, list=21%, signal=34% | |
2869 | REGULATION OF INTERFERON-GAMMA BIOSYNTHETIC PROCESS | 22 | -0.35 | -0.96 | 0.491 | 0.814 | 1.000 | 25520 | tags=59%, list=47%, signal=111% | |
2870 | L-AMINO ACID TRANSPORT | 68 | -0.25 | -0.96 | 0.519 | 0.814 | 1.000 | 25451 | tags=54%, list=47%, signal=102% | |
2871 | REGULATION OF PINOCYTOSIS | 14 | -0.37 | -0.96 | 0.543 | 0.814 | 1.000 | 6752 | tags=29%, list=12%, signal=33% | |
2872 | REGULATION OF REGULATED SECRETORY PATHWAY | 102 | -0.26 | -0.96 | 0.516 | 0.814 | 1.000 | 17066 | tags=37%, list=31%, signal=54% | |
2873 | HISTONE H4-R3 METHYLATION | 8 | -0.44 | -0.96 | 0.527 | 0.814 | 1.000 | 26114 | tags=88%, list=48%, signal=167% | |
2874 | NEGATIVE REGULATION OF PROTEIN COMPLEX ASSEMBLY | 170 | -0.24 | -0.96 | 0.561 | 0.814 | 1.000 | 19479 | tags=40%, list=36%, signal=62% | |
2875 | ENDOTHELIUM DEVELOPMENT | 157 | -0.25 | -0.96 | 0.566 | 0.814 | 1.000 | 29963 | tags=61%, list=55%, signal=133% | |
2876 | POSITIVE REGULATION OF MAINTENANCE OF SISTER CHROMATID COHESION | 9 | -0.42 | -0.96 | 0.541 | 0.814 | 1.000 | 28774 | tags=89%, list=53%, signal=188% | |
2877 | POSITIVE REGULATION OF MAINTENANCE OF MITOTIC SISTER CHROMATID COHESION | 9 | -0.42 | -0.96 | 0.541 | 0.814 | 1.000 | 28774 | tags=89%, list=53%, signal=188% | |
2878 | POSITIVE REGULATION OF SISTER CHROMATID COHESION | 9 | -0.42 | -0.96 | 0.541 | 0.814 | 1.000 | 28774 | tags=89%, list=53%, signal=188% | |
2879 | ORGANIC ACID BIOSYNTHETIC PROCESS | 339 | -0.24 | -0.96 | 0.531 | 0.814 | 1.000 | 27742 | tags=55%, list=51%, signal=112% | |
2880 | CARBOXYLIC ACID BIOSYNTHETIC PROCESS | 339 | -0.24 | -0.96 | 0.531 | 0.814 | 1.000 | 27742 | tags=55%, list=51%, signal=112% | |
2881 | REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 88 | -0.27 | -0.96 | 0.594 | 0.813 | 1.000 | 28364 | tags=60%, list=52%, signal=125% | |
2882 | REGULATION OF ATP METABOLIC PROCESS | 88 | -0.27 | -0.96 | 0.594 | 0.813 | 1.000 | 28364 | tags=60%, list=52%, signal=125% | |
2883 | ATP-DEPENDENT CHROMATIN REMODELING | 146 | -0.27 | -0.96 | 0.573 | 0.814 | 1.000 | 13982 | tags=36%, list=26%, signal=48% | |
2884 | REGULATION OF MDA-5 SIGNALING PATHWAY | 6 | -0.44 | -0.96 | 0.511 | 0.814 | 1.000 | 5108 | tags=33%, list=9%, signal=37% | |
2885 | POSITIVE REGULATION OF B CELL ACTIVATION | 83 | -0.26 | -0.96 | 0.522 | 0.813 | 1.000 | 5072 | tags=18%, list=9%, signal=20% | |
2886 | EPITHELIAL TO MESENCHYMAL TRANSITION | 92 | -0.25 | -0.96 | 0.533 | 0.813 | 1.000 | 25277 | tags=50%, list=46%, signal=93% | |
2887 | CELLULAR RESPONSE TO ORGANIC CYCLIC COMPOUND | 516 | -0.23 | -0.96 | 0.593 | 0.813 | 1.000 | 16328 | tags=33%, list=30%, signal=47% | |
2888 | PEPTIDYL-GLUTAMIC ACID MODIFICATION | 50 | -0.28 | -0.96 | 0.543 | 0.814 | 1.000 | 16919 | tags=44%, list=31%, signal=64% | |
2889 | NITRIC OXIDE METABOLIC PROCESS | 77 | -0.26 | -0.96 | 0.546 | 0.814 | 1.000 | 11503 | tags=29%, list=21%, signal=36% | |
2890 | NEGATIVE REGULATION OF GLUCOCORTICOID RECEPTOR SIGNALING PATHWAY | 14 | -0.34 | -0.96 | 0.534 | 0.814 | 1.000 | 27941 | tags=71%, list=51%, signal=146% | |
2891 | DOUBLE-STRAND BREAK REPAIR VIA SYNTHESIS-DEPENDENT STRAND ANNEALING | 56 | -0.28 | -0.96 | 0.553 | 0.814 | 1.000 | 29901 | tags=66%, list=55%, signal=146% | |
2892 | GLYCOLIPID BIOSYNTHETIC PROCESS | 92 | -0.28 | -0.96 | 0.577 | 0.815 | 1.000 | 22240 | tags=53%, list=41%, signal=90% | |
2893 | REGULATION OF CELLULAR CARBOHYDRATE METABOLIC PROCESS | 237 | -0.24 | -0.96 | 0.609 | 0.815 | 1.000 | 29286 | tags=58%, list=54%, signal=124% | |
2894 | REGULATION OF CARBOHYDRATE BIOSYNTHETIC PROCESS | 128 | -0.23 | -0.96 | 0.552 | 0.814 | 1.000 | 14129 | tags=30%, list=26%, signal=40% | |
2895 | NEGATIVE REGULATION OF SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 58 | -0.28 | -0.96 | 0.532 | 0.815 | 1.000 | 21540 | tags=50%, list=39%, signal=82% | |
2896 | NEGATIVE REGULATION OF ION TRANSPORT | 182 | -0.23 | -0.96 | 0.519 | 0.814 | 1.000 | 20219 | tags=41%, list=37%, signal=64% | |
2897 | MICROTUBULE POLYMERIZATION | 59 | -0.30 | -0.96 | 0.557 | 0.814 | 1.000 | 32706 | tags=80%, list=60%, signal=198% | |
2898 | FLAVONOID METABOLIC PROCESS | 16 | -0.39 | -0.96 | 0.513 | 0.814 | 1.000 | 28882 | tags=81%, list=53%, signal=172% | |
2899 | POSITIVE REGULATION OF CYTOKINE PRODUCTION | 647 | -0.24 | -0.96 | 0.557 | 0.815 | 1.000 | 17031 | tags=35%, list=31%, signal=51% | |
2900 | PROTEIN MYRISTOYLATION | 18 | -0.37 | -0.96 | 0.562 | 0.815 | 1.000 | 26999 | tags=78%, list=49%, signal=154% | |
2901 | REGULATION OF CENTROSOME DUPLICATION | 59 | -0.30 | -0.96 | 0.508 | 0.815 | 1.000 | 26834 | tags=63%, list=49%, signal=123% | |
2902 | PROTEIN HOMOTETRAMERIZATION | 104 | -0.27 | -0.96 | 0.595 | 0.815 | 1.000 | 25054 | tags=56%, list=46%, signal=103% | |
2903 | DEVELOPMENTAL MATURATION | 157 | -0.22 | -0.96 | 0.556 | 0.814 | 1.000 | 18860 | tags=34%, list=34%, signal=51% | |
2904 | CEREBELLAR PURKINJE CELL LAYER DEVELOPMENT | 11 | -0.34 | -0.96 | 0.522 | 0.814 | 1.000 | 24501 | tags=64%, list=45%, signal=115% | |
2905 | CEREBELLAR PURKINJE CELL LAYER MORPHOGENESIS | 11 | -0.34 | -0.96 | 0.522 | 0.814 | 1.000 | 24501 | tags=64%, list=45%, signal=115% | |
2906 | NEGATIVE REGULATION OF DEFENSE RESPONSE | 178 | -0.27 | -0.95 | 0.569 | 0.815 | 1.000 | 23466 | tags=51%, list=43%, signal=88% | |
2907 | AMMONIUM TRANSPORT | 84 | -0.26 | -0.95 | 0.557 | 0.814 | 1.000 | 17806 | tags=39%, list=33%, signal=58% | |
2908 | REGULATION OF INSULIN SECRETION | 293 | -0.23 | -0.95 | 0.545 | 0.815 | 1.000 | 22598 | tags=43%, list=41%, signal=73% | |
2909 | LEFT/RIGHT PATTERN FORMATION | 21 | -0.32 | -0.95 | 0.505 | 0.815 | 1.000 | 4503 | tags=24%, list=8%, signal=26% | |
2910 | ARGININE METABOLIC PROCESS | 15 | -0.33 | -0.95 | 0.522 | 0.815 | 1.000 | 12646 | tags=33%, list=23%, signal=43% | |
2911 | ARGININE CATABOLIC PROCESS | 15 | -0.33 | -0.95 | 0.522 | 0.814 | 1.000 | 12646 | tags=33%, list=23%, signal=43% | |
2912 | NEGATIVE REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 41 | -0.31 | -0.95 | 0.536 | 0.815 | 1.000 | 7049 | tags=22%, list=13%, signal=25% | |
2913 | CYCLIC PURINE NUCLEOTIDE METABOLIC PROCESS | 61 | -0.27 | -0.95 | 0.502 | 0.815 | 1.000 | 11449 | tags=26%, list=21%, signal=33% | |
2914 | CAVEOLIN-MEDIATED ENDOCYTOSIS | 14 | -0.34 | -0.95 | 0.487 | 0.815 | 1.000 | 21479 | tags=57%, list=39%, signal=94% | |
2915 | ACTIN FILAMENT POLYMERIZATION | 39 | -0.30 | -0.95 | 0.552 | 0.815 | 1.000 | 21327 | tags=54%, list=39%, signal=88% | |
2916 | SMAD PROTEIN SIGNAL TRANSDUCTION | 53 | -0.28 | -0.95 | 0.538 | 0.815 | 1.000 | 28769 | tags=58%, list=53%, signal=123% | |
2917 | WNT SIGNALING PATHWAY, PLANAR CELL POLARITY PATHWAY | 15 | -0.31 | -0.95 | 0.522 | 0.815 | 1.000 | 19696 | tags=40%, list=36%, signal=63% | |
2918 | POSITIVE REGULATION OF INSULIN RECEPTOR SIGNALING PATHWAY | 10 | -0.39 | -0.95 | 0.520 | 0.815 | 1.000 | 10308 | tags=30%, list=19%, signal=37% | |
2919 | POSITIVE REGULATION OF MAPK CASCADE | 1095 | -0.22 | -0.95 | 0.589 | 0.815 | 1.000 | 21395 | tags=40%, list=39%, signal=65% | |
2920 | POSITIVE REGULATION OF ACTIVATED T CELL PROLIFERATION | 39 | -0.25 | -0.95 | 0.521 | 0.815 | 1.000 | 13287 | tags=31%, list=24%, signal=41% | |
2921 | MHC PROTEIN COMPLEX ASSEMBLY | 13 | -0.44 | -0.95 | 0.529 | 0.816 | 1.000 | 22598 | tags=77%, list=41%, signal=131% | |
2922 | PEPTIDE ANTIGEN ASSEMBLY WITH MHC PROTEIN COMPLEX | 13 | -0.44 | -0.95 | 0.529 | 0.815 | 1.000 | 22598 | tags=77%, list=41%, signal=131% | |
2923 | SOMATIC DIVERSIFICATION OF IMMUNOGLOBULINS | 44 | -0.27 | -0.95 | 0.552 | 0.815 | 1.000 | 18286 | tags=41%, list=33%, signal=61% | |
2924 | REGULATION OF SPHINGOLIPID BIOSYNTHETIC PROCESS | 15 | -0.37 | -0.95 | 0.537 | 0.816 | 1.000 | 17124 | tags=53%, list=31%, signal=78% | |
2925 | REGULATION OF CERAMIDE BIOSYNTHETIC PROCESS | 15 | -0.37 | -0.95 | 0.537 | 0.815 | 1.000 | 17124 | tags=53%, list=31%, signal=78% | |
2926 | CELLULAR RESPONSE TO VASCULAR ENDOTHELIAL GROWTH FACTOR STIMULUS | 64 | -0.27 | -0.95 | 0.528 | 0.815 | 1.000 | 12072 | tags=27%, list=22%, signal=34% | |
2927 | POSITIVE REGULATION OF NEUROTRANSMITTER TRANSPORT | 23 | -0.32 | -0.95 | 0.531 | 0.816 | 1.000 | 13980 | tags=39%, list=26%, signal=53% | |
2928 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION INVOLVED IN INFLAMMATORY RESPONSE | 5 | -0.48 | -0.95 | 0.539 | 0.816 | 1.000 | 28237 | tags=100%, list=52%, signal=207% | |
2929 | NEGATIVE REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 131 | -0.23 | -0.95 | 0.521 | 0.817 | 1.000 | 30641 | tags=57%, list=56%, signal=130% | |
2930 | REGULATION OF FATTY ACID BIOSYNTHETIC PROCESS | 48 | -0.26 | -0.95 | 0.548 | 0.817 | 1.000 | 19756 | tags=42%, list=36%, signal=65% | |
2931 | REGULATION OF CELL GROWTH | 522 | -0.22 | -0.95 | 0.639 | 0.817 | 1.000 | 28737 | tags=55%, list=53%, signal=116% | |
2932 | VITAMIN CATABOLIC PROCESS | 9 | -0.40 | -0.95 | 0.507 | 0.819 | 1.000 | 26960 | tags=67%, list=49%, signal=131% | |
2933 | HISTONE H3-K4 METHYLATION | 71 | -0.29 | -0.95 | 0.569 | 0.819 | 1.000 | 23006 | tags=49%, list=42%, signal=85% | |
2934 | ANATOMICAL STRUCTURE MATURATION | 38 | -0.27 | -0.95 | 0.542 | 0.819 | 1.000 | 18711 | tags=34%, list=34%, signal=52% | |
2935 | POSITIVE REGULATION OF LIPID METABOLIC PROCESS | 212 | -0.23 | -0.95 | 0.548 | 0.819 | 1.000 | 23829 | tags=45%, list=44%, signal=79% | |
2936 | CELL FATE COMMITMENT | 212 | -0.22 | -0.95 | 0.559 | 0.819 | 1.000 | 22985 | tags=44%, list=42%, signal=75% | |
2937 | SKIN EPIDERMIS DEVELOPMENT | 54 | -0.27 | -0.95 | 0.534 | 0.820 | 1.000 | 29991 | tags=61%, list=55%, signal=135% | |
2938 | ENDOCYTOSIS | 836 | -0.23 | -0.95 | 0.546 | 0.819 | 1.000 | 23401 | tags=45%, list=43%, signal=78% | |
2939 | POSITIVE REGULATION OF MITOTIC CELL CYCLE PHASE TRANSITION | 88 | -0.27 | -0.95 | 0.614 | 0.820 | 1.000 | 24924 | tags=56%, list=46%, signal=102% | |
2940 | NEGATIVE REGULATION OF VIRAL TRANSCRIPTION | 64 | -0.28 | -0.95 | 0.578 | 0.820 | 1.000 | 34667 | tags=81%, list=63%, signal=222% | |
2941 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 108 | -0.25 | -0.95 | 0.548 | 0.821 | 1.000 | 25169 | tags=53%, list=46%, signal=98% | |
2942 | NEGATIVE REGULATION OF TOLL-LIKE RECEPTOR SIGNALING PATHWAY | 34 | -0.31 | -0.95 | 0.534 | 0.821 | 1.000 | 32672 | tags=68%, list=60%, signal=168% | |
2943 | POSITIVE REGULATION OF MYELOID CELL DIFFERENTIATION | 121 | -0.24 | -0.95 | 0.585 | 0.821 | 1.000 | 24937 | tags=45%, list=46%, signal=82% | |
2944 | NEGATIVE REGULATION OF GLUCOSE IMPORT | 19 | -0.33 | -0.95 | 0.521 | 0.821 | 1.000 | 11672 | tags=32%, list=21%, signal=40% | |
2945 | REGULATION OF GLOMERULAR FILTRATION | 17 | -0.31 | -0.95 | 0.569 | 0.821 | 1.000 | 22100 | tags=59%, list=40%, signal=99% | |
2946 | LEUKOTRIENE SIGNALING PATHWAY | 10 | -0.37 | -0.95 | 0.520 | 0.821 | 1.000 | 29838 | tags=80%, list=55%, signal=176% | |
2947 | CARTILAGE CONDENSATION | 13 | -0.37 | -0.95 | 0.507 | 0.821 | 1.000 | 6904 | tags=23%, list=13%, signal=26% | |
2948 | CELL AGGREGATION | 13 | -0.37 | -0.95 | 0.507 | 0.820 | 1.000 | 6904 | tags=23%, list=13%, signal=26% | |
2949 | REGULATION OF GLYCOGEN METABOLIC PROCESS | 67 | -0.25 | -0.95 | 0.566 | 0.820 | 1.000 | 12145 | tags=28%, list=22%, signal=36% | |
2950 | REGULATION OF TYPE I INTERFERON-MEDIATED SIGNALING PATHWAY | 80 | -0.25 | -0.95 | 0.592 | 0.820 | 1.000 | 28948 | tags=58%, list=53%, signal=122% | |
2951 | POSITIVE REGULATION OF MYELOID CELL APOPTOTIC PROCESS | 8 | -0.40 | -0.95 | 0.554 | 0.821 | 1.000 | 27588 | tags=75%, list=50%, signal=151% | |
2952 | NEGATIVE REGULATION OF NATURAL KILLER CELL MEDIATED IMMUNITY | 19 | -0.38 | -0.95 | 0.550 | 0.821 | 1.000 | 13927 | tags=47%, list=25%, signal=64% | |
2953 | NEGATIVE REGULATION OF NATURAL KILLER CELL MEDIATED CYTOTOXICITY | 19 | -0.38 | -0.95 | 0.550 | 0.821 | 1.000 | 13927 | tags=47%, list=25%, signal=64% | |
2954 | VESICLE DOCKING INVOLVED IN EXOCYTOSIS | 21 | -0.32 | -0.95 | 0.547 | 0.821 | 1.000 | 15868 | tags=43%, list=29%, signal=60% | |
2955 | RESPONSE TO BIOTIC STIMULUS | 1025 | -0.23 | -0.95 | 0.590 | 0.822 | 1.000 | 23967 | tags=47%, list=44%, signal=83% | |
2956 | REGULATION OF CYTOKINE-MEDIATED SIGNALING PATHWAY | 247 | -0.24 | -0.95 | 0.585 | 0.822 | 1.000 | 18785 | tags=38%, list=34%, signal=58% | |
2957 | POSITIVE REGULATION OF CELL DEVELOPMENT | 658 | -0.22 | -0.95 | 0.618 | 0.821 | 1.000 | 28697 | tags=54%, list=52%, signal=113% | |
2958 | CHONDROITIN SULFATE PROTEOGLYCAN METABOLIC PROCESS | 119 | -0.24 | -0.95 | 0.535 | 0.821 | 1.000 | 21261 | tags=43%, list=39%, signal=70% | |
2959 | POSITIVE REGULATION OF CELL CYCLE PHASE TRANSITION | 104 | -0.27 | -0.95 | 0.603 | 0.821 | 1.000 | 24924 | tags=55%, list=46%, signal=101% | |
2960 | PHAGOCYTOSIS | 405 | -0.23 | -0.95 | 0.516 | 0.821 | 1.000 | 23507 | tags=45%, list=43%, signal=79% | |
2961 | SPHINGOLIPID METABOLIC PROCESS | 221 | -0.25 | -0.95 | 0.587 | 0.821 | 1.000 | 24401 | tags=51%, list=45%, signal=92% | |
2962 | ORGANIC ACID TRANSPORT | 394 | -0.22 | -0.95 | 0.603 | 0.821 | 1.000 | 25451 | tags=49%, list=47%, signal=91% | |
2963 | ACTOMYOSIN STRUCTURE ORGANIZATION | 144 | -0.24 | -0.95 | 0.555 | 0.821 | 1.000 | 21818 | tags=44%, list=40%, signal=74% | |
2964 | CYTOPLASMIC MICROTUBULE ORGANIZATION | 65 | -0.30 | -0.95 | 0.563 | 0.821 | 1.000 | 29050 | tags=66%, list=53%, signal=141% | |
2965 | POSITIVE REGULATION OF T CELL MEDIATED IMMUNITY | 66 | -0.27 | -0.95 | 0.541 | 0.821 | 1.000 | 17597 | tags=39%, list=32%, signal=58% | |
2966 | PEPTIDYL-ARGININE MODIFICATION | 29 | -0.31 | -0.95 | 0.545 | 0.821 | 1.000 | 26114 | tags=66%, list=48%, signal=125% | |
2967 | REGULATION OF PEPTIDE SECRETION | 349 | -0.22 | -0.95 | 0.577 | 0.821 | 1.000 | 22598 | tags=42%, list=41%, signal=71% | |
2968 | REGULATION OF ERYTHROCYTE DIFFERENTIATION | 63 | -0.26 | -0.95 | 0.544 | 0.821 | 1.000 | 32890 | tags=67%, list=60%, signal=167% | |
2969 | POSITIVE REGULATION OF GENE SILENCING BY MIRNA | 16 | -0.33 | -0.94 | 0.538 | 0.821 | 1.000 | 22464 | tags=56%, list=41%, signal=95% | |
2970 | POSITIVE REGULATION OF POSTTRANSCRIPTIONAL GENE SILENCING | 19 | -0.33 | -0.94 | 0.531 | 0.821 | 1.000 | 27407 | tags=68%, list=50%, signal=137% | |
2971 | ESTABLISHMENT OF MELANOSOME LOCALIZATION | 25 | -0.34 | -0.94 | 0.563 | 0.821 | 1.000 | 24273 | tags=64%, list=44%, signal=115% | |
2972 | ESTABLISHMENT OF PIGMENT GRANULE LOCALIZATION | 25 | -0.34 | -0.94 | 0.563 | 0.821 | 1.000 | 24273 | tags=64%, list=44%, signal=115% | |
2973 | PROTEIN LOCALIZATION TO KINETOCHORE | 20 | -0.32 | -0.94 | 0.576 | 0.820 | 1.000 | 15241 | tags=40%, list=28%, signal=55% | |
2974 | FATTY ACID BIOSYNTHETIC PROCESS | 120 | -0.26 | -0.94 | 0.569 | 0.820 | 1.000 | 28795 | tags=61%, list=53%, signal=128% | |
2975 | CARNITINE TRANSMEMBRANE TRANSPORT | 35 | -0.31 | -0.94 | 0.573 | 0.820 | 1.000 | 22600 | tags=57%, list=41%, signal=97% | |
2976 | PURINE-CONTAINING COMPOUND TRANSMEMBRANE TRANSPORT | 16 | -0.33 | -0.94 | 0.552 | 0.820 | 1.000 | 33229 | tags=75%, list=61%, signal=191% | |
2977 | RESPONSE TO PROSTAGLANDIN | 36 | -0.29 | -0.94 | 0.550 | 0.820 | 1.000 | 8920 | tags=28%, list=16%, signal=33% | |
2978 | REGULATION OF PEPTIDE HORMONE SECRETION | 346 | -0.22 | -0.94 | 0.578 | 0.820 | 1.000 | 22598 | tags=42%, list=41%, signal=71% | |
2979 | REGULATION OF MESODERM DEVELOPMENT | 18 | -0.31 | -0.94 | 0.519 | 0.820 | 1.000 | 31642 | tags=67%, list=58%, signal=158% | |
2980 | MACROPHAGE ACTIVATION | 39 | -0.31 | -0.94 | 0.537 | 0.820 | 1.000 | 19607 | tags=46%, list=36%, signal=72% | |
2981 | TELOMERE CAPPING | 23 | -0.33 | -0.94 | 0.565 | 0.820 | 1.000 | 12657 | tags=39%, list=23%, signal=51% | |
2982 | NEGATIVE REGULATION OF PROTEIN TRANSPORT | 331 | -0.23 | -0.94 | 0.600 | 0.820 | 1.000 | 28812 | tags=55%, list=53%, signal=116% | |
2983 | GLUCURONATE CATABOLIC PROCESS | 10 | -0.36 | -0.94 | 0.524 | 0.820 | 1.000 | 21159 | tags=60%, list=39%, signal=98% | |
2984 | GLUCURONATE CATABOLIC PROCESS TO XYLULOSE 5-PHOSPHATE | 10 | -0.36 | -0.94 | 0.524 | 0.820 | 1.000 | 21159 | tags=60%, list=39%, signal=98% | |
2985 | XYLULOSE 5-PHOSPHATE METABOLIC PROCESS | 10 | -0.36 | -0.94 | 0.524 | 0.819 | 1.000 | 21159 | tags=60%, list=39%, signal=98% | |
2986 | XYLULOSE 5-PHOSPHATE BIOSYNTHETIC PROCESS | 10 | -0.36 | -0.94 | 0.524 | 0.819 | 1.000 | 21159 | tags=60%, list=39%, signal=98% | |
2987 | ANION TRANSMEMBRANE TRANSPORT | 383 | -0.23 | -0.94 | 0.603 | 0.819 | 1.000 | 24828 | tags=48%, list=45%, signal=86% | |
2988 | PHOSPHOLIPID EFFLUX | 25 | -0.34 | -0.94 | 0.549 | 0.819 | 1.000 | 21536 | tags=48%, list=39%, signal=79% | |
2989 | CHONDROITIN SULFATE METABOLIC PROCESS | 117 | -0.24 | -0.94 | 0.549 | 0.820 | 1.000 | 21261 | tags=43%, list=39%, signal=70% | |
2990 | REGULATION OF FATTY ACID OXIDATION | 64 | -0.27 | -0.94 | 0.576 | 0.819 | 1.000 | 13870 | tags=33%, list=25%, signal=44% | |
2991 | NEGATIVE REGULATION OF GROWTH | 328 | -0.23 | -0.94 | 0.593 | 0.819 | 1.000 | 28908 | tags=55%, list=53%, signal=116% | |
2992 | SNRNA TRANSCRIPTION FROM RNA POLYMERASE III PROMOTER | 6 | -0.41 | -0.94 | 0.539 | 0.820 | 1.000 | 30021 | tags=83%, list=55%, signal=185% | |
2993 | REGULATION OF CELL DEVELOPMENT | 1107 | -0.22 | -0.94 | 0.664 | 0.820 | 1.000 | 28569 | tags=54%, list=52%, signal=111% | |
2994 | LINOLEIC ACID METABOLIC PROCESS | 25 | -0.31 | -0.94 | 0.576 | 0.820 | 1.000 | 26115 | tags=60%, list=48%, signal=115% | |
2995 | POSITIVE REGULATION OF PROTEIN DEACETYLATION | 41 | -0.29 | -0.94 | 0.585 | 0.820 | 1.000 | 23278 | tags=54%, list=43%, signal=93% | |
2996 | POSITIVE REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 131 | -0.25 | -0.94 | 0.541 | 0.820 | 1.000 | 18538 | tags=38%, list=34%, signal=58% | |
2997 | ESTABLISHMENT OF ENDOTHELIAL INTESTINAL BARRIER | 24 | -0.33 | -0.94 | 0.560 | 0.820 | 1.000 | 25751 | tags=63%, list=47%, signal=118% | |
2998 | RESPONSE TO EXTERNAL BIOTIC STIMULUS | 992 | -0.23 | -0.94 | 0.591 | 0.820 | 1.000 | 24622 | tags=48%, list=45%, signal=86% | |
2999 | RESPONSE TO OTHER ORGANISM | 992 | -0.23 | -0.94 | 0.591 | 0.820 | 1.000 | 24622 | tags=48%, list=45%, signal=86% | |
3000 | DNA METHYLATION ON CYTOSINE | 41 | -0.29 | -0.94 | 0.521 | 0.820 | 1.000 | 28239 | tags=61%, list=52%, signal=126% | |
3001 | LEFT/RIGHT AXIS SPECIFICATION | 17 | -0.32 | -0.94 | 0.522 | 0.819 | 1.000 | 4503 | tags=24%, list=8%, signal=26% | |
3002 | LUNG DEVELOPMENT | 97 | -0.24 | -0.94 | 0.564 | 0.819 | 1.000 | 17992 | tags=37%, list=33%, signal=55% | |
3003 | WATER HOMEOSTASIS | 119 | -0.23 | -0.94 | 0.550 | 0.819 | 1.000 | 20922 | tags=39%, list=38%, signal=64% | |
3004 | MULTICELLULAR ORGANISMAL WATER HOMEOSTASIS | 119 | -0.23 | -0.94 | 0.550 | 0.819 | 1.000 | 20922 | tags=39%, list=38%, signal=64% | |
3005 | POSITIVE REGULATION OF PHOSPHATIDYLINOSITOL 3-KINASE ACTIVITY | 50 | -0.25 | -0.94 | 0.525 | 0.819 | 1.000 | 22664 | tags=42%, list=41%, signal=72% | |
3006 | NUCLEAR PORE ORGANIZATION | 24 | -0.36 | -0.94 | 0.549 | 0.819 | 1.000 | 23874 | tags=67%, list=44%, signal=118% | |
3007 | REGULATION OF RECEPTOR RECYCLING | 32 | -0.29 | -0.94 | 0.564 | 0.819 | 1.000 | 17166 | tags=44%, list=31%, signal=64% | |
3008 | CYCLIC NUCLEOTIDE BIOSYNTHETIC PROCESS | 64 | -0.27 | -0.94 | 0.512 | 0.819 | 1.000 | 11449 | tags=27%, list=21%, signal=34% | |
3009 | REGULATION OF TUMOR NECROSIS FACTOR PRODUCTION | 145 | -0.26 | -0.94 | 0.548 | 0.819 | 1.000 | 20636 | tags=42%, list=38%, signal=67% | |
3010 | CELLULAR PROTEIN COMPLEX LOCALIZATION | 30 | -0.32 | -0.94 | 0.547 | 0.819 | 1.000 | 23235 | tags=57%, list=42%, signal=98% | |
3011 | CARBOXYLIC ACID TRANSPORT | 390 | -0.22 | -0.94 | 0.614 | 0.819 | 1.000 | 25451 | tags=49%, list=47%, signal=91% | |
3012 | REGULATION OF PROTEIN LOCALIZATION TO SYNAPSE | 10 | -0.35 | -0.94 | 0.523 | 0.818 | 1.000 | 7326 | tags=30%, list=13%, signal=35% | |
3013 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO SYNAPSE | 10 | -0.35 | -0.94 | 0.523 | 0.818 | 1.000 | 7326 | tags=30%, list=13%, signal=35% | |
3014 | POSITIVE REGULATION OF GLIAL CELL DIFFERENTIATION | 25 | -0.32 | -0.94 | 0.530 | 0.818 | 1.000 | 32436 | tags=76%, list=59%, signal=187% | |
3015 | CELLULAR KETONE BODY METABOLIC PROCESS | 15 | -0.33 | -0.94 | 0.556 | 0.818 | 1.000 | 19720 | tags=47%, list=36%, signal=73% | |
3016 | KETONE BODY METABOLIC PROCESS | 15 | -0.33 | -0.94 | 0.556 | 0.817 | 1.000 | 19720 | tags=47%, list=36%, signal=73% | |
3017 | CELLULAR RESPONSE TO KETONE | 69 | -0.25 | -0.94 | 0.569 | 0.818 | 1.000 | 13491 | tags=29%, list=25%, signal=38% | |
3018 | POSITIVE REGULATION OF DEPHOSPHORYLATION | 87 | -0.26 | -0.94 | 0.583 | 0.818 | 1.000 | 30637 | tags=66%, list=56%, signal=149% | |
3019 | POSITIVE REGULATION OF PROTEIN DEPHOSPHORYLATION | 87 | -0.26 | -0.94 | 0.583 | 0.818 | 1.000 | 30637 | tags=66%, list=56%, signal=149% | |
3020 | REGULATION OF MEMBRANE REPOLARIZATION | 47 | -0.24 | -0.94 | 0.585 | 0.818 | 1.000 | 15979 | tags=32%, list=29%, signal=45% | |
3021 | NEGATIVE REGULATION OF LIPOPROTEIN PARTICLE CLEARANCE | 12 | -0.39 | -0.94 | 0.558 | 0.818 | 1.000 | 19183 | tags=50%, list=35%, signal=77% | |
3022 | GLYCERALDEHYDE-3-PHOSPHATE METABOLIC PROCESS | 36 | -0.27 | -0.94 | 0.559 | 0.818 | 1.000 | 27465 | tags=61%, list=50%, signal=123% | |
3023 | TUBE MORPHOGENESIS | 323 | -0.22 | -0.94 | 0.587 | 0.818 | 1.000 | 31201 | tags=58%, list=57%, signal=135% | |
3024 | NEGATIVE REGULATION OF NOTCH SIGNALING PATHWAY | 38 | -0.27 | -0.94 | 0.569 | 0.818 | 1.000 | 26808 | tags=55%, list=49%, signal=108% | |
3025 | REGULATION OF ADAPTIVE IMMUNE RESPONSE BASED ON SOMATIC RECOMBINATION OF IMMUNE RECEPTORS BUILT FROM IMMUNOGLOBULIN SUPERFAMILY DOMAINS | 165 | -0.25 | -0.94 | 0.543 | 0.819 | 1.000 | 9842 | tags=25%, list=18%, signal=31% | |
3026 | CELL-MATRIX ADHESION | 185 | -0.23 | -0.94 | 0.579 | 0.818 | 1.000 | 21962 | tags=42%, list=40%, signal=69% | |
3027 | SODIUM ION HOMEOSTASIS | 44 | -0.26 | -0.94 | 0.572 | 0.819 | 1.000 | 26237 | tags=52%, list=48%, signal=100% | |
3028 | CENTROSOME ORGANIZATION | 143 | -0.26 | -0.94 | 0.597 | 0.819 | 1.000 | 32637 | tags=73%, list=60%, signal=182% | |
3029 | MYELOID LEUKOCYTE DIFFERENTIATION | 101 | -0.25 | -0.94 | 0.583 | 0.820 | 1.000 | 22943 | tags=46%, list=42%, signal=78% | |
3030 | POSITIVE REGULATION OF ADAPTIVE IMMUNE RESPONSE BASED ON SOMATIC RECOMBINATION OF IMMUNE RECEPTORS BUILT FROM IMMUNOGLOBULIN SUPERFAMILY DOMAINS | 95 | -0.25 | -0.94 | 0.575 | 0.821 | 1.000 | 17837 | tags=39%, list=33%, signal=58% | |
3031 | HEME TRANSPORT | 12 | -0.35 | -0.94 | 0.548 | 0.821 | 1.000 | 15454 | tags=50%, list=28%, signal=70% | |
3032 | OSTEOBLAST DEVELOPMENT | 13 | -0.32 | -0.94 | 0.560 | 0.822 | 1.000 | 5728 | tags=23%, list=10%, signal=26% | |
3033 | RESPIRATORY SYSTEM DEVELOPMENT | 114 | -0.24 | -0.94 | 0.579 | 0.822 | 1.000 | 17992 | tags=37%, list=33%, signal=55% | |
3034 | L-ASCORBIC ACID METABOLIC PROCESS | 21 | -0.37 | -0.94 | 0.632 | 0.822 | 1.000 | 12525 | tags=43%, list=23%, signal=56% | |
3035 | JUN PHOSPHORYLATION | 10 | -0.41 | -0.94 | 0.594 | 0.821 | 1.000 | 16675 | tags=60%, list=30%, signal=86% | |
3036 | PROTEIN HOMOTRIMERIZATION | 25 | -0.29 | -0.94 | 0.529 | 0.821 | 1.000 | 31219 | tags=68%, list=57%, signal=158% | |
3037 | NEGATIVE REGULATION OF ENDOPEPTIDASE ACTIVITY | 369 | -0.24 | -0.94 | 0.605 | 0.821 | 1.000 | 20653 | tags=43%, list=38%, signal=69% | |
3038 | EMBRYO DEVELOPMENT ENDING IN BIRTH OR EGG HATCHING | 280 | -0.22 | -0.94 | 0.618 | 0.821 | 1.000 | 28363 | tags=54%, list=52%, signal=111% | |
3039 | CHORDATE EMBRYONIC DEVELOPMENT | 280 | -0.22 | -0.94 | 0.618 | 0.821 | 1.000 | 28363 | tags=54%, list=52%, signal=111% | |
3040 | NECROPTOTIC SIGNALING PATHWAY | 11 | -0.37 | -0.94 | 0.543 | 0.821 | 1.000 | 13785 | tags=45%, list=25%, signal=61% | |
3041 | POST-EMBRYONIC DEVELOPMENT | 33 | -0.29 | -0.94 | 0.533 | 0.821 | 1.000 | 28154 | tags=61%, list=51%, signal=125% | |
3042 | POSITIVE REGULATION OF FIBROBLAST APOPTOTIC PROCESS | 28 | -0.30 | -0.94 | 0.568 | 0.821 | 1.000 | 13770 | tags=39%, list=25%, signal=52% | |
3043 | CELLULAR RESPONSE TO ACID CHEMICAL | 213 | -0.23 | -0.94 | 0.595 | 0.821 | 1.000 | 20305 | tags=40%, list=37%, signal=64% | |
3044 | GRANULOCYTE ACTIVATION | 27 | -0.33 | -0.94 | 0.562 | 0.822 | 1.000 | 23006 | tags=56%, list=42%, signal=96% | |
3045 | NEGATIVE REGULATION OF TRANSPORT | 695 | -0.22 | -0.94 | 0.604 | 0.822 | 1.000 | 23310 | tags=44%, list=43%, signal=76% | |
3046 | REGULATION OF TRANSLATIONAL ELONGATION | 14 | -0.34 | -0.94 | 0.548 | 0.822 | 1.000 | 18498 | tags=50%, list=34%, signal=76% | |
3047 | REGULATION OF HISTONE H3-K27 METHYLATION | 25 | -0.33 | -0.94 | 0.565 | 0.822 | 1.000 | 13746 | tags=40%, list=25%, signal=53% | |
3048 | REGULATION OF ANTIGEN PROCESSING AND PRESENTATION | 49 | -0.29 | -0.94 | 0.549 | 0.822 | 1.000 | 5047 | tags=20%, list=9%, signal=22% | |
3049 | PROTEIN DEPHOSPHORYLATION | 342 | -0.25 | -0.94 | 0.617 | 0.822 | 1.000 | 23009 | tags=50%, list=42%, signal=85% | |
3050 | MONOVALENT INORGANIC CATION TRANSPORT | 547 | -0.21 | -0.94 | 0.563 | 0.822 | 1.000 | 19026 | tags=36%, list=35%, signal=54% | |
3051 | POSITIVE REGULATION OF SPHINGOLIPID BIOSYNTHETIC PROCESS | 13 | -0.37 | -0.94 | 0.558 | 0.822 | 1.000 | 17124 | tags=54%, list=31%, signal=78% | |
3052 | POSITIVE REGULATION OF CERAMIDE BIOSYNTHETIC PROCESS | 13 | -0.37 | -0.94 | 0.558 | 0.822 | 1.000 | 17124 | tags=54%, list=31%, signal=78% | |
3053 | NEGATIVE REGULATION OF MAPK CASCADE | 265 | -0.25 | -0.93 | 0.609 | 0.823 | 1.000 | 23235 | tags=47%, list=42%, signal=81% | |
3054 | MICROTUBULE ORGANIZING CENTER ORGANIZATION | 158 | -0.26 | -0.93 | 0.581 | 0.824 | 1.000 | 32706 | tags=73%, list=60%, signal=182% | |
3055 | REGULATION OF DENDRITE DEVELOPMENT | 181 | -0.22 | -0.93 | 0.635 | 0.823 | 1.000 | 27838 | tags=57%, list=51%, signal=117% | |
3056 | POSITIVE REGULATION OF TUMOR NECROSIS FACTOR SUPERFAMILY CYTOKINE PRODUCTION | 79 | -0.28 | -0.93 | 0.559 | 0.824 | 1.000 | 16757 | tags=38%, list=31%, signal=55% | |
3057 | OSTEOCLAST DIFFERENTIATION | 40 | -0.28 | -0.93 | 0.598 | 0.825 | 1.000 | 22516 | tags=50%, list=41%, signal=85% | |
3058 | QUATERNARY AMMONIUM GROUP TRANSPORT | 38 | -0.29 | -0.93 | 0.582 | 0.825 | 1.000 | 22600 | tags=55%, list=41%, signal=94% | |
3059 | TOXIN TRANSPORT | 13 | -0.35 | -0.93 | 0.560 | 0.825 | 1.000 | 18134 | tags=46%, list=33%, signal=69% | |
3060 | PYRIMIDINE-CONTAINING COMPOUND CATABOLIC PROCESS | 63 | -0.25 | -0.93 | 0.598 | 0.825 | 1.000 | 29684 | tags=63%, list=54%, signal=139% | |
3061 | POSITIVE REGULATION OF EPIDERMAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 28 | -0.30 | -0.93 | 0.541 | 0.825 | 1.000 | 12800 | tags=32%, list=23%, signal=42% | |
3062 | ICOSANOID METABOLIC PROCESS | 135 | -0.24 | -0.93 | 0.571 | 0.825 | 1.000 | 29272 | tags=62%, list=54%, signal=134% | |
3063 | FATTY ACID DERIVATIVE METABOLIC PROCESS | 135 | -0.24 | -0.93 | 0.571 | 0.825 | 1.000 | 29272 | tags=62%, list=54%, signal=134% | |
3064 | GLUTAMINE FAMILY AMINO ACID CATABOLIC PROCESS | 40 | -0.28 | -0.93 | 0.577 | 0.825 | 1.000 | 24403 | tags=52%, list=45%, signal=95% | |
3065 | CRANIAL SKELETAL SYSTEM DEVELOPMENT | 50 | -0.27 | -0.93 | 0.565 | 0.825 | 1.000 | 30993 | tags=62%, list=57%, signal=143% | |
3066 | PURINE NUCLEOBASE TRANSPORT | 7 | -0.39 | -0.93 | 0.538 | 0.825 | 1.000 | 18588 | tags=57%, list=34%, signal=87% | |
3067 | NORADRENERGIC NEURON DIFFERENTIATION | 15 | -0.34 | -0.93 | 0.521 | 0.825 | 1.000 | 35937 | tags=93%, list=66%, signal=272% | |
3068 | POSITIVE REGULATION OF LIPID KINASE ACTIVITY | 52 | -0.25 | -0.93 | 0.531 | 0.826 | 1.000 | 22664 | tags=42%, list=41%, signal=72% | |
3069 | REGULATION OF CYTOSKELETON ORGANIZATION | 690 | -0.23 | -0.93 | 0.666 | 0.826 | 1.000 | 30488 | tags=60%, list=56%, signal=134% | |
3070 | MOLTING CYCLE PROCESS | 54 | -0.26 | -0.93 | 0.542 | 0.825 | 1.000 | 15881 | tags=35%, list=29%, signal=50% | |
3071 | HAIR CYCLE PROCESS | 54 | -0.26 | -0.93 | 0.542 | 0.825 | 1.000 | 15881 | tags=35%, list=29%, signal=50% | |
3072 | NEGATIVE REGULATION OF NEURON PROJECTION DEVELOPMENT | 126 | -0.26 | -0.93 | 0.652 | 0.825 | 1.000 | 28569 | tags=63%, list=52%, signal=131% | |
3073 | PURINE NUCLEOSIDE TRANSMEMBRANE TRANSPORT | 12 | -0.35 | -0.93 | 0.558 | 0.825 | 1.000 | 33229 | tags=75%, list=61%, signal=191% | |
3074 | MODULATION BY HOST OF VIRAL TRANSCRIPTION | 59 | -0.27 | -0.93 | 0.608 | 0.825 | 1.000 | 17839 | tags=41%, list=33%, signal=60% | |
3075 | MODULATION OF TRANSCRIPTION IN OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 59 | -0.27 | -0.93 | 0.608 | 0.825 | 1.000 | 17839 | tags=41%, list=33%, signal=60% | |
3076 | MODULATION BY HOST OF SYMBIONT TRANSCRIPTION | 59 | -0.27 | -0.93 | 0.608 | 0.824 | 1.000 | 17839 | tags=41%, list=33%, signal=60% | |
3077 | INDUCTION OF POSITIVE CHEMOTAXIS | 10 | -0.38 | -0.93 | 0.537 | 0.824 | 1.000 | 1605 | tags=20%, list=3%, signal=21% | |
3078 | SUBSTRATE ADHESION-DEPENDENT CELL SPREADING | 85 | -0.25 | -0.93 | 0.542 | 0.824 | 1.000 | 35599 | tags=80%, list=65%, signal=229% | |
3079 | NEGATIVE REGULATION OF EPIDERMAL GROWTH FACTOR-ACTIVATED RECEPTOR ACTIVITY | 17 | -0.32 | -0.93 | 0.557 | 0.825 | 1.000 | 27121 | tags=65%, list=50%, signal=128% | |
3080 | RESPONSE TO UV-B | 17 | -0.32 | -0.93 | 0.537 | 0.825 | 1.000 | 8380 | tags=29%, list=15%, signal=35% | |
3081 | TRANSEPITHELIAL TRANSPORT | 26 | -0.28 | -0.93 | 0.567 | 0.825 | 1.000 | 15656 | tags=38%, list=29%, signal=54% | |
3082 | EPITHELIUM DEVELOPMENT | 956 | -0.21 | -0.93 | 0.673 | 0.825 | 1.000 | 28384 | tags=53%, list=52%, signal=107% | |
3083 | REGULATION OF MICROTUBULE-BASED PROCESS | 290 | -0.24 | -0.93 | 0.601 | 0.825 | 1.000 | 26174 | tags=54%, list=48%, signal=104% | |
3084 | NUCLEOSOME ASSEMBLY | 135 | -0.26 | -0.93 | 0.652 | 0.825 | 1.000 | 28896 | tags=61%, list=53%, signal=129% | |
3085 | PROTEIN DEMANNOSYLATION | 17 | -0.35 | -0.93 | 0.541 | 0.825 | 1.000 | 10024 | tags=35%, list=18%, signal=43% | |
3086 | PROTEIN ALPHA-1,2-DEMANNOSYLATION | 17 | -0.35 | -0.93 | 0.541 | 0.825 | 1.000 | 10024 | tags=35%, list=18%, signal=43% | |
3087 | NEGATIVE REGULATION OF ADAPTIVE IMMUNE RESPONSE | 58 | -0.31 | -0.93 | 0.590 | 0.825 | 1.000 | 5307 | tags=21%, list=10%, signal=23% | |
3088 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO TELOMERE | 10 | -0.37 | -0.93 | 0.580 | 0.825 | 1.000 | 24022 | tags=70%, list=44%, signal=125% | |
3089 | PURINE-CONTAINING COMPOUND CATABOLIC PROCESS | 92 | -0.25 | -0.93 | 0.614 | 0.825 | 1.000 | 27362 | tags=54%, list=50%, signal=109% | |
3090 | B CELL DIFFERENTIATION | 97 | -0.23 | -0.93 | 0.589 | 0.825 | 1.000 | 29422 | tags=57%, list=54%, signal=123% | |
3091 | REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 28 | -0.28 | -0.93 | 0.543 | 0.825 | 1.000 | 11503 | tags=36%, list=21%, signal=45% | |
3092 | POSITIVE REGULATION OF PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 33 | -0.29 | -0.93 | 0.594 | 0.825 | 1.000 | 31989 | tags=70%, list=59%, signal=168% | |
3093 | NEGATIVE REGULATION OF MEMBRANE POTENTIAL | 9 | -0.40 | -0.93 | 0.586 | 0.826 | 1.000 | 20820 | tags=67%, list=38%, signal=108% | |
3094 | REGULATION OF VASCULAR SMOOTH MUSCLE CELL PROLIFERATION | 6 | -0.44 | -0.93 | 0.557 | 0.826 | 1.000 | 24337 | tags=67%, list=45%, signal=120% | |
3095 | VESICLE DOCKING | 24 | -0.30 | -0.93 | 0.597 | 0.826 | 1.000 | 15868 | tags=42%, list=29%, signal=59% | |
3096 | POSITIVE REGULATION OF INTERFERON-ALPHA PRODUCTION | 31 | -0.34 | -0.93 | 0.594 | 0.826 | 1.000 | 17597 | tags=48%, list=32%, signal=71% | |
3097 | NEGATIVE REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 11 | -0.37 | -0.93 | 0.569 | 0.826 | 1.000 | 28457 | tags=73%, list=52%, signal=152% | |
3098 | NEGATIVE REGULATION OF AXON EXTENSION | 16 | -0.36 | -0.93 | 0.542 | 0.826 | 1.000 | 28543 | tags=81%, list=52%, signal=170% | |
3099 | REGULATION OF LAMELLIPODIUM ASSEMBLY | 36 | -0.29 | -0.93 | 0.588 | 0.827 | 1.000 | 19435 | tags=42%, list=36%, signal=65% | |
3100 | REGULATION OF REPRODUCTIVE PROCESS | 93 | -0.25 | -0.93 | 0.593 | 0.826 | 1.000 | 22260 | tags=44%, list=41%, signal=74% | |
3101 | AXON GUIDANCE | 1360 | -0.21 | -0.93 | 0.672 | 0.827 | 1.000 | 26865 | tags=49%, list=49%, signal=94% | |
3102 | NEURON PROJECTION GUIDANCE | 1360 | -0.21 | -0.93 | 0.672 | 0.826 | 1.000 | 26865 | tags=49%, list=49%, signal=94% | |
3103 | REGULATION OF ACTIN FILAMENT DEPOLYMERIZATION | 58 | -0.26 | -0.93 | 0.623 | 0.826 | 1.000 | 19184 | tags=43%, list=35%, signal=66% | |
3104 | SPINDLE MIDZONE ASSEMBLY | 8 | -0.38 | -0.93 | 0.585 | 0.826 | 1.000 | 30730 | tags=88%, list=56%, signal=200% | |
3105 | MITOTIC SPINDLE MIDZONE ASSEMBLY | 8 | -0.38 | -0.93 | 0.585 | 0.826 | 1.000 | 30730 | tags=88%, list=56%, signal=200% | |
3106 | HEMOPOIESIS | 532 | -0.22 | -0.93 | 0.640 | 0.825 | 1.000 | 22516 | tags=43%, list=41%, signal=72% | |
3107 | NEGATIVE REGULATION OF NEURON APOPTOTIC PROCESS | 112 | -0.24 | -0.93 | 0.628 | 0.825 | 1.000 | 22028 | tags=44%, list=40%, signal=73% | |
3108 | REGULATION OF DENDRITIC SPINE MORPHOGENESIS | 67 | -0.25 | -0.93 | 0.618 | 0.825 | 1.000 | 26607 | tags=58%, list=49%, signal=113% | |
3109 | RAC PROTEIN SIGNAL TRANSDUCTION | 27 | -0.30 | -0.93 | 0.601 | 0.825 | 1.000 | 22819 | tags=56%, list=42%, signal=95% | |
3110 | VENTRICULAR SEPTUM MORPHOGENESIS | 42 | -0.26 | -0.93 | 0.579 | 0.825 | 1.000 | 23708 | tags=50%, list=43%, signal=88% | |
3111 | METAL ION HOMEOSTASIS | 678 | -0.22 | -0.93 | 0.609 | 0.825 | 1.000 | 19611 | tags=37%, list=36%, signal=57% | |
3112 | RESPONSE TO CORTICOSTEROID | 48 | -0.28 | -0.93 | 0.616 | 0.825 | 1.000 | 20883 | tags=42%, list=38%, signal=67% | |
3113 | POSITIVE REGULATION OF TOLERANCE INDUCTION | 12 | -0.40 | -0.93 | 0.584 | 0.825 | 1.000 | 16824 | tags=58%, list=31%, signal=84% | |
3114 | NEGATIVE REGULATION OF LEUKOCYTE CELL-CELL ADHESION | 135 | -0.25 | -0.93 | 0.602 | 0.825 | 1.000 | 24197 | tags=48%, list=44%, signal=86% | |
3115 | POSITIVE REGULATION OF HORMONE SECRETION | 132 | -0.24 | -0.93 | 0.572 | 0.825 | 1.000 | 23143 | tags=47%, list=42%, signal=81% | |
3116 | BODY MORPHOGENESIS | 49 | -0.27 | -0.93 | 0.597 | 0.826 | 1.000 | 14053 | tags=33%, list=26%, signal=44% | |
3117 | REGULATION OF SECRETION | 944 | -0.21 | -0.93 | 0.637 | 0.826 | 1.000 | 22043 | tags=41%, list=40%, signal=67% | |
3118 | MITOTIC CHROMOSOME CONDENSATION | 20 | -0.30 | -0.93 | 0.578 | 0.826 | 1.000 | 16278 | tags=40%, list=30%, signal=57% | |
3119 | AMINO ACID TRANSPORT | 188 | -0.22 | -0.93 | 0.590 | 0.826 | 1.000 | 23198 | tags=44%, list=42%, signal=76% | |
3120 | REGULATION OF P38MAPK CASCADE | 50 | -0.29 | -0.93 | 0.547 | 0.827 | 1.000 | 25293 | tags=56%, list=46%, signal=104% | |
3121 | AMINE BIOSYNTHETIC PROCESS | 26 | -0.29 | -0.93 | 0.564 | 0.827 | 1.000 | 5870 | tags=19%, list=11%, signal=22% | |
3122 | SARCOPLASMIC RETICULUM CALCIUM ION TRANSPORT | 21 | -0.29 | -0.92 | 0.580 | 0.828 | 1.000 | 5008 | tags=19%, list=9%, signal=21% | |
3123 | MAMMARY GLAND EPITHELIUM DEVELOPMENT | 45 | -0.26 | -0.92 | 0.589 | 0.827 | 1.000 | 25311 | tags=49%, list=46%, signal=91% | |
3124 | MAINTENANCE OF ORGANELLE LOCATION | 14 | -0.32 | -0.92 | 0.576 | 0.827 | 1.000 | 23805 | tags=57%, list=44%, signal=101% | |
3125 | POSITIVE REGULATION OF INTERFERON-BETA PRODUCTION | 54 | -0.31 | -0.92 | 0.607 | 0.827 | 1.000 | 15474 | tags=43%, list=28%, signal=59% | |
3126 | REGULATION OF MEMBRANE LIPID DISTRIBUTION | 26 | -0.30 | -0.92 | 0.583 | 0.827 | 1.000 | 31236 | tags=69%, list=57%, signal=161% | |
3127 | CELLULAR RESPONSE TO ALCOHOL | 112 | -0.22 | -0.92 | 0.637 | 0.827 | 1.000 | 29343 | tags=55%, list=54%, signal=119% | |
3128 | NEGATIVE REGULATION OF T CELL ACTIVATION | 118 | -0.25 | -0.92 | 0.600 | 0.827 | 1.000 | 17156 | tags=36%, list=31%, signal=52% | |
3129 | DEFENSE RESPONSE TO GRAM-POSITIVE BACTERIUM | 77 | -0.26 | -0.92 | 0.561 | 0.827 | 1.000 | 25828 | tags=53%, list=47%, signal=101% | |
3130 | MYELOID CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 39 | -0.30 | -0.92 | 0.597 | 0.827 | 1.000 | 22504 | tags=46%, list=41%, signal=78% | |
3131 | REGULATION OF NUCLEAR-TRANSCRIBED MRNA CATABOLIC PROCESS, DEADENYLATION-DEPENDENT DECAY | 39 | -0.28 | -0.92 | 0.576 | 0.827 | 1.000 | 30368 | tags=69%, list=56%, signal=156% | |
3132 | POSITIVE REGULATION OF NUCLEAR-TRANSCRIBED MRNA CATABOLIC PROCESS, DEADENYLATION-DEPENDENT DECAY | 39 | -0.28 | -0.92 | 0.576 | 0.827 | 1.000 | 30368 | tags=69%, list=56%, signal=156% | |
3133 | DETERMINATION OF BILATERAL SYMMETRY | 125 | -0.24 | -0.92 | 0.570 | 0.827 | 1.000 | 33971 | tags=70%, list=62%, signal=183% | |
3134 | ACTIVATION OF MAPK ACTIVITY | 222 | -0.23 | -0.92 | 0.599 | 0.827 | 1.000 | 20401 | tags=40%, list=37%, signal=64% | |
3135 | EMBRYONIC HEART TUBE DEVELOPMENT | 94 | -0.24 | -0.92 | 0.587 | 0.827 | 1.000 | 33971 | tags=69%, list=62%, signal=182% | |
3136 | IMMUNE SYSTEM DEVELOPMENT | 610 | -0.22 | -0.92 | 0.631 | 0.827 | 1.000 | 22516 | tags=42%, list=41%, signal=71% | |
3137 | LYMPHOID PROGENITOR CELL DIFFERENTIATION | 13 | -0.35 | -0.92 | 0.567 | 0.826 | 1.000 | 25567 | tags=69%, list=47%, signal=130% | |
3138 | NUCLEUS LOCALIZATION | 20 | -0.34 | -0.92 | 0.574 | 0.826 | 1.000 | 29005 | tags=70%, list=53%, signal=149% | |
3139 | NEGATIVE REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 30 | -0.29 | -0.92 | 0.574 | 0.826 | 1.000 | 13224 | tags=30%, list=24%, signal=40% | |
3140 | MEMBRANE INVAGINATION | 49 | -0.26 | -0.92 | 0.605 | 0.827 | 1.000 | 18559 | tags=41%, list=34%, signal=62% | |
3141 | REGULATION OF CELL-SUBSTRATE ADHESION | 340 | -0.22 | -0.92 | 0.657 | 0.827 | 1.000 | 33078 | tags=66%, list=60%, signal=166% | |
3142 | GDP-MANNOSE BIOSYNTHETIC PROCESS | 8 | -0.39 | -0.92 | 0.559 | 0.827 | 1.000 | 18997 | tags=63%, list=35%, signal=96% | |
3143 | SCHWANN CELL DEVELOPMENT | 30 | -0.31 | -0.92 | 0.597 | 0.827 | 1.000 | 28517 | tags=70%, list=52%, signal=146% | |
3144 | MYELINATION IN PERIPHERAL NERVOUS SYSTEM | 30 | -0.31 | -0.92 | 0.597 | 0.827 | 1.000 | 28517 | tags=70%, list=52%, signal=146% | |
3145 | PERIPHERAL NERVOUS SYSTEM AXON ENSHEATHMENT | 30 | -0.31 | -0.92 | 0.597 | 0.827 | 1.000 | 28517 | tags=70%, list=52%, signal=146% | |
3146 | CARDIAC MUSCLE CELL-CARDIAC MUSCLE CELL ADHESION | 13 | -0.37 | -0.92 | 0.568 | 0.827 | 1.000 | 31662 | tags=77%, list=58%, signal=183% | |
3147 | BUNDLE OF HIS CELL-PURKINJE MYOCYTE ADHESION INVOLVED IN CELL COMMUNICATION | 13 | -0.37 | -0.92 | 0.568 | 0.827 | 1.000 | 31662 | tags=77%, list=58%, signal=183% | |
3148 | REGULATION OF LIPID METABOLIC PROCESS | 437 | -0.22 | -0.92 | 0.678 | 0.826 | 1.000 | 29616 | tags=56%, list=54%, signal=121% | |
3149 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE III PROMOTER | 16 | -0.32 | -0.92 | 0.561 | 0.827 | 1.000 | 30021 | tags=75%, list=55%, signal=166% | |
3150 | MODULATION BY HOST OF VIRAL PROCESS | 40 | -0.27 | -0.92 | 0.616 | 0.826 | 1.000 | 20245 | tags=48%, list=37%, signal=75% | |
3151 | MITOCHONDRIAL DNA REPLICATION | 3 | -0.52 | -0.92 | 0.614 | 0.827 | 1.000 | 13249 | tags=67%, list=24%, signal=88% | |
3152 | OUTFLOW TRACT SEPTUM MORPHOGENESIS | 34 | -0.28 | -0.92 | 0.536 | 0.827 | 1.000 | 21813 | tags=44%, list=40%, signal=73% | |
3153 | REGULATION OF GRANULOCYTE CHEMOTAXIS | 53 | -0.28 | -0.92 | 0.558 | 0.827 | 1.000 | 19058 | tags=40%, list=35%, signal=61% | |
3154 | ARACHIDONIC ACID METABOLIC PROCESS | 103 | -0.25 | -0.92 | 0.592 | 0.827 | 1.000 | 28804 | tags=63%, list=53%, signal=133% | |
3155 | REGULATION OF EPIDERMAL GROWTH FACTOR-ACTIVATED RECEPTOR ACTIVITY | 39 | -0.28 | -0.92 | 0.609 | 0.827 | 1.000 | 28741 | tags=62%, list=53%, signal=130% | |
3156 | ERROR-PRONE TRANSLESION SYNTHESIS | 36 | -0.32 | -0.92 | 0.575 | 0.827 | 1.000 | 29624 | tags=75%, list=54%, signal=164% | |
3157 | ACTIVATION OF ADENYLATE CYCLASE ACTIVITY | 64 | -0.26 | -0.92 | 0.574 | 0.827 | 1.000 | 20178 | tags=36%, list=37%, signal=57% | |
3158 | REGULATION OF SECRETION BY CELL | 873 | -0.21 | -0.92 | 0.639 | 0.827 | 1.000 | 23432 | tags=43%, list=43%, signal=75% | |
3159 | PHAGOLYSOSOME ASSEMBLY | 12 | -0.37 | -0.92 | 0.578 | 0.827 | 1.000 | 25770 | tags=67%, list=47%, signal=126% | |
3160 | HEMATOPOIETIC OR LYMPHOID ORGAN DEVELOPMENT | 572 | -0.22 | -0.92 | 0.645 | 0.827 | 1.000 | 22516 | tags=42%, list=41%, signal=71% | |
3161 | BMP SIGNALING PATHWAY | 133 | -0.24 | -0.92 | 0.642 | 0.828 | 1.000 | 15477 | tags=33%, list=28%, signal=46% | |
3162 | NEUTRAL LIPID CATABOLIC PROCESS | 56 | -0.25 | -0.92 | 0.588 | 0.828 | 1.000 | 23759 | tags=48%, list=43%, signal=85% | |
3163 | ACYLGLYCEROL CATABOLIC PROCESS | 56 | -0.25 | -0.92 | 0.588 | 0.827 | 1.000 | 23759 | tags=48%, list=43%, signal=85% | |
3164 | PLASMA MEMBRANE FUSION | 10 | -0.36 | -0.92 | 0.563 | 0.827 | 1.000 | 20796 | tags=50%, list=38%, signal=81% | |
3165 | HETEROCHROMATIN ORGANIZATION | 34 | -0.28 | -0.92 | 0.617 | 0.827 | 1.000 | 15092 | tags=35%, list=28%, signal=49% | |
3166 | EARLY ENDOSOME TO LATE ENDOSOME TRANSPORT | 53 | -0.29 | -0.92 | 0.601 | 0.827 | 1.000 | 18914 | tags=47%, list=35%, signal=72% | |
3167 | RESPONSE TO MONOAMINE | 59 | -0.27 | -0.92 | 0.611 | 0.827 | 1.000 | 11573 | tags=29%, list=21%, signal=37% | |
3168 | CELLULAR RESPONSE TO MONOAMINE STIMULUS | 59 | -0.27 | -0.92 | 0.611 | 0.827 | 1.000 | 11573 | tags=29%, list=21%, signal=37% | |
3169 | RESPONSE TO CATECHOLAMINE | 59 | -0.27 | -0.92 | 0.611 | 0.827 | 1.000 | 11573 | tags=29%, list=21%, signal=37% | |
3170 | CELLULAR RESPONSE TO CATECHOLAMINE STIMULUS | 59 | -0.27 | -0.92 | 0.611 | 0.826 | 1.000 | 11573 | tags=29%, list=21%, signal=37% | |
3171 | RESPONSE TO OXYGEN RADICAL | 19 | -0.35 | -0.92 | 0.607 | 0.826 | 1.000 | 12354 | tags=37%, list=23%, signal=48% | |
3172 | RESPONSE TO TRANSITION METAL NANOPARTICLE | 101 | -0.25 | -0.92 | 0.588 | 0.827 | 1.000 | 15796 | tags=34%, list=29%, signal=47% | |
3173 | NEGATIVE REGULATION OF ALPHA-BETA T CELL ACTIVATION | 50 | -0.26 | -0.92 | 0.605 | 0.827 | 1.000 | 9842 | tags=24%, list=18%, signal=29% | |
3174 | FEMALE MEIOTIC DIVISION | 17 | -0.32 | -0.92 | 0.558 | 0.827 | 1.000 | 33393 | tags=76%, list=61%, signal=196% | |
3175 | REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 96 | -0.23 | -0.92 | 0.593 | 0.827 | 1.000 | 23829 | tags=44%, list=44%, signal=77% | |
3176 | STEROL METABOLIC PROCESS | 146 | -0.23 | -0.92 | 0.603 | 0.828 | 1.000 | 25118 | tags=49%, list=46%, signal=91% | |
3177 | HIGH-DENSITY LIPOPROTEIN PARTICLE ASSEMBLY | 14 | -0.36 | -0.92 | 0.552 | 0.828 | 1.000 | 16252 | tags=43%, list=30%, signal=61% | |
3178 | RESPONSE TO LIPOPROTEIN PARTICLE | 38 | -0.29 | -0.92 | 0.588 | 0.827 | 1.000 | 30049 | tags=71%, list=55%, signal=158% | |
3179 | POSITIVE REGULATION OF SKELETAL MUSCLE TISSUE DEVELOPMENT | 34 | -0.27 | -0.92 | 0.553 | 0.827 | 1.000 | 14571 | tags=32%, list=27%, signal=44% | |
3180 | CELLULAR POTASSIUM ION HOMEOSTASIS | 15 | -0.34 | -0.92 | 0.589 | 0.827 | 1.000 | 23366 | tags=60%, list=43%, signal=105% | |
3181 | DEVELOPMENTAL GROWTH | 235 | -0.22 | -0.92 | 0.685 | 0.828 | 1.000 | 16694 | tags=33%, list=31%, signal=48% | |
3182 | NEGATIVE REGULATION OF HOMOTYPIC CELL-CELL ADHESION | 135 | -0.24 | -0.92 | 0.618 | 0.828 | 1.000 | 17156 | tags=35%, list=31%, signal=51% | |
3183 | NUCLEAR BODY ORGANIZATION | 30 | -0.30 | -0.92 | 0.577 | 0.828 | 1.000 | 22427 | tags=47%, list=41%, signal=79% | |
3184 | NEGATIVE REGULATION OF FATTY ACID METABOLIC PROCESS | 42 | -0.28 | -0.92 | 0.559 | 0.828 | 1.000 | 29616 | tags=64%, list=54%, signal=140% | |
3185 | CATION HOMEOSTASIS | 740 | -0.21 | -0.92 | 0.651 | 0.828 | 1.000 | 19611 | tags=37%, list=36%, signal=57% | |
3186 | REGULATION OF HUMORAL IMMUNE RESPONSE | 69 | -0.25 | -0.92 | 0.610 | 0.829 | 1.000 | 28382 | tags=58%, list=52%, signal=120% | |
3187 | MATURE RIBOSOME ASSEMBLY | 12 | -0.38 | -0.92 | 0.581 | 0.829 | 1.000 | 17272 | tags=50%, list=32%, signal=73% | |
3188 | NEGATIVE REGULATION OF PEPTIDASE ACTIVITY | 378 | -0.24 | -0.92 | 0.641 | 0.828 | 1.000 | 20653 | tags=43%, list=38%, signal=68% | |
3189 | PROTEIN PALMITOYLATION | 46 | -0.24 | -0.92 | 0.595 | 0.828 | 1.000 | 3443 | tags=17%, list=6%, signal=19% | |
3190 | CENTRIOLE ASSEMBLY | 45 | -0.25 | -0.92 | 0.574 | 0.829 | 1.000 | 32637 | tags=69%, list=60%, signal=171% | |
3191 | CELL ACTIVATION | 1064 | -0.22 | -0.92 | 0.594 | 0.829 | 1.000 | 21811 | tags=42%, list=40%, signal=68% | |
3192 | MONOCARBOXYLIC ACID TRANSPORT | 181 | -0.24 | -0.92 | 0.681 | 0.829 | 1.000 | 31864 | tags=66%, list=58%, signal=158% | |
3193 | RESPONSE TO ALCOHOL | 208 | -0.21 | -0.92 | 0.642 | 0.829 | 1.000 | 19816 | tags=37%, list=36%, signal=57% | |
3194 | REGULATION OF GLIAL CELL APOPTOTIC PROCESS | 17 | -0.31 | -0.92 | 0.548 | 0.829 | 1.000 | 13664 | tags=35%, list=25%, signal=47% | |
3195 | NEGATIVE REGULATION OF GLIAL CELL APOPTOTIC PROCESS | 17 | -0.31 | -0.92 | 0.548 | 0.829 | 1.000 | 13664 | tags=35%, list=25%, signal=47% | |
3196 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO OXIDATIVE STRESS | 17 | -0.35 | -0.92 | 0.568 | 0.829 | 1.000 | 14185 | tags=47%, list=26%, signal=64% | |
3197 | CELL DEATH IN RESPONSE TO OXIDATIVE STRESS | 17 | -0.35 | -0.92 | 0.568 | 0.829 | 1.000 | 14185 | tags=47%, list=26%, signal=64% | |
3198 | PROTEIN HOMOOLIGOMERIZATION | 313 | -0.24 | -0.92 | 0.634 | 0.829 | 1.000 | 25163 | tags=51%, list=46%, signal=95% | |
3199 | POSITIVE REGULATION OF AXON EXTENSION INVOLVED IN AXON GUIDANCE | 16 | -0.32 | -0.91 | 0.577 | 0.831 | 1.000 | 28038 | tags=63%, list=51%, signal=128% | |
3200 | POSITIVE REGULATION OF AXON GUIDANCE | 16 | -0.32 | -0.91 | 0.577 | 0.830 | 1.000 | 28038 | tags=63%, list=51%, signal=128% | |
3201 | G-PROTEIN COUPLED ACETYLCHOLINE RECEPTOR SIGNALING PATHWAY | 43 | -0.26 | -0.91 | 0.581 | 0.831 | 1.000 | 16916 | tags=37%, list=31%, signal=54% | |
3202 | POSITIVE REGULATION OF MONOCYTE DIFFERENTIATION | 8 | -0.38 | -0.91 | 0.568 | 0.832 | 1.000 | 15231 | tags=38%, list=28%, signal=52% | |
3203 | POSITIVE REGULATION OF VASCULAR PERMEABILITY | 13 | -0.34 | -0.91 | 0.590 | 0.832 | 1.000 | 6538 | tags=23%, list=12%, signal=26% | |
3204 | POSITIVE REGULATION OF CELL GROWTH | 241 | -0.22 | -0.91 | 0.670 | 0.832 | 1.000 | 30336 | tags=59%, list=55%, signal=133% | |
3205 | THYROID HORMONE METABOLIC PROCESS | 19 | -0.31 | -0.91 | 0.573 | 0.832 | 1.000 | 14270 | tags=37%, list=26%, signal=50% | |
3206 | DEVELOPMENTAL GROWTH INVOLVED IN MORPHOGENESIS | 89 | -0.23 | -0.91 | 0.602 | 0.832 | 1.000 | 16029 | tags=34%, list=29%, signal=48% | |
3207 | REGULATION OF BRANCHING INVOLVED IN URETERIC BUD MORPHOGENESIS | 35 | -0.26 | -0.91 | 0.583 | 0.833 | 1.000 | 17093 | tags=34%, list=31%, signal=50% | |
3208 | MALE GAMETE GENERATION | 292 | -0.21 | -0.91 | 0.678 | 0.833 | 1.000 | 24273 | tags=45%, list=44%, signal=80% | |
3209 | REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 805 | -0.21 | -0.91 | 0.702 | 0.832 | 1.000 | 28569 | tags=53%, list=52%, signal=110% | |
3210 | POSITIVE REGULATION OF DENDRITE DEVELOPMENT | 83 | -0.23 | -0.91 | 0.621 | 0.832 | 1.000 | 28697 | tags=59%, list=52%, signal=124% | |
3211 | FATTY ACID TRANSPORT | 93 | -0.25 | -0.91 | 0.642 | 0.833 | 1.000 | 24104 | tags=54%, list=44%, signal=96% | |
3212 | POSITIVE REGULATION OF PRI-MIRNA TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 22 | -0.32 | -0.91 | 0.593 | 0.833 | 1.000 | 34205 | tags=86%, list=63%, signal=231% | |
3213 | T CELL APOPTOTIC PROCESS | 12 | -0.34 | -0.91 | 0.604 | 0.833 | 1.000 | 17275 | tags=50%, list=32%, signal=73% | |
3214 | SPERMATOGENESIS | 290 | -0.21 | -0.91 | 0.675 | 0.833 | 1.000 | 24273 | tags=44%, list=44%, signal=80% | |
3215 | PROTEIN LOCALIZATION TO CHROMOSOME, CENTROMERIC REGION | 24 | -0.30 | -0.91 | 0.624 | 0.833 | 1.000 | 28896 | tags=63%, list=53%, signal=132% | |
3216 | POSITIVE REGULATION OF RECEPTOR ACTIVITY | 125 | -0.23 | -0.91 | 0.606 | 0.833 | 1.000 | 12137 | tags=26%, list=22%, signal=34% | |
3217 | PROTEIN-DNA COMPLEX ASSEMBLY | 162 | -0.25 | -0.91 | 0.658 | 0.833 | 1.000 | 31843 | tags=68%, list=58%, signal=162% | |
3218 | REGULATION OF ACTIN CYTOSKELETON ORGANIZATION | 437 | -0.22 | -0.91 | 0.663 | 0.832 | 1.000 | 30488 | tags=59%, list=56%, signal=131% | |
3219 | MONOCARBOXYLIC ACID BIOSYNTHETIC PROCESS | 209 | -0.23 | -0.91 | 0.620 | 0.833 | 1.000 | 28825 | tags=58%, list=53%, signal=122% | |
3220 | POSITIVE REGULATION OF MAST CELL ACTIVATION | 14 | -0.36 | -0.91 | 0.592 | 0.833 | 1.000 | 15751 | tags=50%, list=29%, signal=70% | |
3221 | POSITIVE REGULATION OF IMMUNE EFFECTOR PROCESS | 219 | -0.23 | -0.91 | 0.626 | 0.833 | 1.000 | 11592 | tags=26%, list=21%, signal=32% | |
3222 | REGULATION OF PROTEIN ACTIVATION CASCADE | 61 | -0.25 | -0.91 | 0.615 | 0.835 | 1.000 | 28382 | tags=59%, list=52%, signal=123% | |
3223 | DIGESTIVE TRACT DEVELOPMENT | 116 | -0.22 | -0.91 | 0.638 | 0.834 | 1.000 | 17788 | tags=34%, list=33%, signal=50% | |
3224 | DIGESTIVE SYSTEM DEVELOPMENT | 116 | -0.22 | -0.91 | 0.638 | 0.834 | 1.000 | 17788 | tags=34%, list=33%, signal=50% | |
3225 | PORPHYRIN-CONTAINING COMPOUND CATABOLIC PROCESS | 15 | -0.37 | -0.91 | 0.560 | 0.834 | 1.000 | 31625 | tags=87%, list=58%, signal=206% | |
3226 | TETRAPYRROLE CATABOLIC PROCESS | 15 | -0.37 | -0.91 | 0.560 | 0.834 | 1.000 | 31625 | tags=87%, list=58%, signal=206% | |
3227 | HEME CATABOLIC PROCESS | 15 | -0.37 | -0.91 | 0.560 | 0.833 | 1.000 | 31625 | tags=87%, list=58%, signal=206% | |
3228 | PIGMENT CATABOLIC PROCESS | 15 | -0.37 | -0.91 | 0.560 | 0.833 | 1.000 | 31625 | tags=87%, list=58%, signal=206% | |
3229 | NEGATIVE REGULATION OF DELAYED RECTIFIER POTASSIUM CHANNEL ACTIVITY | 18 | -0.34 | -0.91 | 0.555 | 0.833 | 1.000 | 25853 | tags=61%, list=47%, signal=116% | |
3230 | EPITHELIAL TUBE MORPHOGENESIS | 284 | -0.21 | -0.91 | 0.631 | 0.834 | 1.000 | 27726 | tags=51%, list=51%, signal=102% | |
3231 | REGULATION OF FILOPODIUM ASSEMBLY | 73 | -0.25 | -0.91 | 0.616 | 0.834 | 1.000 | 26811 | tags=53%, list=49%, signal=105% | |
3232 | HYDROGEN PEROXIDE METABOLIC PROCESS | 39 | -0.32 | -0.91 | 0.563 | 0.833 | 1.000 | 15100 | tags=41%, list=28%, signal=57% | |
3233 | PERIPHERAL NERVOUS SYSTEM DEVELOPMENT | 91 | -0.23 | -0.91 | 0.657 | 0.834 | 1.000 | 28517 | tags=54%, list=52%, signal=112% | |
3234 | REGULATION OF TYPE B PANCREATIC CELL DEVELOPMENT | 30 | -0.28 | -0.91 | 0.578 | 0.834 | 1.000 | 19317 | tags=40%, list=35%, signal=62% | |
3235 | POSITIVE REGULATION OF LEUKOCYTE CHEMOTAXIS | 109 | -0.25 | -0.91 | 0.598 | 0.834 | 1.000 | 15479 | tags=34%, list=28%, signal=47% | |
3236 | REGULATION OF CILIUM MOVEMENT INVOLVED IN CELL MOTILITY | 9 | -0.40 | -0.91 | 0.550 | 0.834 | 1.000 | 25722 | tags=78%, list=47%, signal=147% | |
3237 | REGULATION OF CILIUM BEAT FREQUENCY INVOLVED IN CILIARY MOTILITY | 9 | -0.40 | -0.91 | 0.550 | 0.833 | 1.000 | 25722 | tags=78%, list=47%, signal=147% | |
3238 | REGULATION OF CILIUM-DEPENDENT CELL MOTILITY | 9 | -0.40 | -0.91 | 0.550 | 0.833 | 1.000 | 25722 | tags=78%, list=47%, signal=147% | |
3239 | POSITIVE REGULATION OF EPIDERMIS DEVELOPMENT | 44 | -0.28 | -0.91 | 0.594 | 0.833 | 1.000 | 29028 | tags=64%, list=53%, signal=136% | |
3240 | HEMIDESMOSOME ASSEMBLY | 34 | -0.27 | -0.91 | 0.540 | 0.833 | 1.000 | 24647 | tags=53%, list=45%, signal=96% | |
3241 | RESPONSE TO NUTRIENT | 75 | -0.26 | -0.91 | 0.640 | 0.833 | 1.000 | 29263 | tags=64%, list=54%, signal=138% | |
3242 | PEPTIDYL-ARGININE OMEGA-N-METHYLATION | 10 | -0.39 | -0.91 | 0.585 | 0.833 | 1.000 | 26114 | tags=80%, list=48%, signal=153% | |
3243 | NUCLEOSIDE TRANSPORT | 22 | -0.29 | -0.91 | 0.602 | 0.833 | 1.000 | 9403 | tags=23%, list=17%, signal=27% | |
3244 | CELLULAR RESPONSE TO LIPOPROTEIN PARTICLE STIMULUS | 26 | -0.31 | -0.91 | 0.586 | 0.833 | 1.000 | 30049 | tags=73%, list=55%, signal=162% | |
3245 | CELLULAR RESPONSE TO LOW-DENSITY LIPOPROTEIN PARTICLE STIMULUS | 26 | -0.31 | -0.91 | 0.586 | 0.833 | 1.000 | 30049 | tags=73%, list=55%, signal=162% | |
3246 | NEUTROPHIL ACTIVATION | 23 | -0.32 | -0.91 | 0.627 | 0.833 | 1.000 | 12087 | tags=35%, list=22%, signal=45% | |
3247 | BUNDLE OF HIS CELL TO PURKINJE MYOCYTE COMMUNICATION | 20 | -0.32 | -0.91 | 0.563 | 0.833 | 1.000 | 32930 | tags=70%, list=60%, signal=176% | |
3248 | SPECIFICATION OF SYMMETRY | 126 | -0.24 | -0.91 | 0.586 | 0.833 | 1.000 | 33971 | tags=69%, list=62%, signal=182% | |
3249 | REGULATION OF MALE GONAD DEVELOPMENT | 12 | -0.35 | -0.91 | 0.589 | 0.833 | 1.000 | 18731 | tags=42%, list=34%, signal=63% | |
3250 | ISOPRENOID CATABOLIC PROCESS | 9 | -0.38 | -0.91 | 0.570 | 0.834 | 1.000 | 28246 | tags=67%, list=52%, signal=138% | |
3251 | NEGATIVE REGULATION OF CELL-CELL ADHESION | 212 | -0.23 | -0.91 | 0.672 | 0.834 | 1.000 | 24197 | tags=47%, list=44%, signal=83% | |
3252 | EMBRYONIC SKELETAL SYSTEM MORPHOGENESIS | 60 | -0.24 | -0.91 | 0.658 | 0.835 | 1.000 | 30993 | tags=57%, list=57%, signal=131% | |
3253 | POSITIVE REGULATION OF LEUKOCYTE MIGRATION | 128 | -0.25 | -0.91 | 0.596 | 0.835 | 1.000 | 15479 | tags=34%, list=28%, signal=48% | |
3254 | HISTONE-SERINE PHOSPHORYLATION | 27 | -0.29 | -0.91 | 0.575 | 0.835 | 1.000 | 25028 | tags=56%, list=46%, signal=102% | |
3255 | REGULATION OF ACTIVIN RECEPTOR SIGNALING PATHWAY | 40 | -0.28 | -0.91 | 0.561 | 0.835 | 1.000 | 19772 | tags=45%, list=36%, signal=70% | |
3256 | AMINO-ACID BETAINE TRANSPORT | 36 | -0.30 | -0.91 | 0.613 | 0.835 | 1.000 | 22600 | tags=56%, list=41%, signal=95% | |
3257 | CARNITINE TRANSPORT | 36 | -0.30 | -0.91 | 0.613 | 0.834 | 1.000 | 22600 | tags=56%, list=41%, signal=95% | |
3258 | MULTICELLULAR ORGANISMAL REPRODUCTIVE PROCESS | 421 | -0.20 | -0.91 | 0.692 | 0.835 | 1.000 | 16098 | tags=31%, list=29%, signal=43% | |
3259 | RESPONSE TO LOW-DENSITY LIPOPROTEIN PARTICLE | 34 | -0.29 | -0.91 | 0.588 | 0.835 | 1.000 | 32454 | tags=76%, list=59%, signal=188% | |
3260 | RECEPTOR CLUSTERING | 50 | -0.26 | -0.91 | 0.559 | 0.835 | 1.000 | 20135 | tags=40%, list=37%, signal=63% | |
3261 | REGULATION OF HYALURONAN BIOSYNTHETIC PROCESS | 15 | -0.32 | -0.91 | 0.555 | 0.836 | 1.000 | 22911 | tags=53%, list=42%, signal=92% | |
3262 | EMBRYONIC PATTERN SPECIFICATION | 67 | -0.25 | -0.91 | 0.639 | 0.836 | 1.000 | 23252 | tags=43%, list=43%, signal=75% | |
3263 | POSITIVE REGULATION OF HORMONE METABOLIC PROCESS | 25 | -0.30 | -0.91 | 0.579 | 0.836 | 1.000 | 21312 | tags=44%, list=39%, signal=72% | |
3264 | POSITIVE REGULATION OF ERBB SIGNALING PATHWAY | 31 | -0.29 | -0.91 | 0.603 | 0.836 | 1.000 | 12800 | tags=32%, list=23%, signal=42% | |
3265 | ALPHA-BETA T CELL ACTIVATION | 60 | -0.26 | -0.91 | 0.629 | 0.836 | 1.000 | 31167 | tags=63%, list=57%, signal=147% | |
3266 | CYTOSKELETAL ANCHORING AT PLASMA MEMBRANE | 17 | -0.30 | -0.90 | 0.592 | 0.836 | 1.000 | 25853 | tags=59%, list=47%, signal=112% | |
3267 | REGULATION OF NUCLEAR-TRANSCRIBED MRNA POLY(A) TAIL SHORTENING | 31 | -0.31 | -0.90 | 0.574 | 0.837 | 1.000 | 31630 | tags=74%, list=58%, signal=176% | |
3268 | POSITIVE REGULATION OF NUCLEAR-TRANSCRIBED MRNA POLY(A) TAIL SHORTENING | 31 | -0.31 | -0.90 | 0.574 | 0.837 | 1.000 | 31630 | tags=74%, list=58%, signal=176% | |
3269 | HEMOSTASIS | 1257 | -0.21 | -0.90 | 0.600 | 0.837 | 1.000 | 28960 | tags=54%, list=53%, signal=112% | |
3270 | REGULATION OF CELL AGING | 73 | -0.25 | -0.90 | 0.622 | 0.837 | 1.000 | 27986 | tags=56%, list=51%, signal=115% | |
3271 | EMBRYONIC SKELETAL SYSTEM DEVELOPMENT | 89 | -0.23 | -0.90 | 0.637 | 0.837 | 1.000 | 24219 | tags=46%, list=44%, signal=83% | |
3272 | SNRNA TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 12 | -0.35 | -0.90 | 0.633 | 0.837 | 1.000 | 12209 | tags=42%, list=22%, signal=54% | |
3273 | LIMBIC SYSTEM DEVELOPMENT | 68 | -0.25 | -0.90 | 0.613 | 0.837 | 1.000 | 31514 | tags=66%, list=58%, signal=156% | |
3274 | NEGATIVE REGULATION OF NEURON DIFFERENTIATION | 175 | -0.24 | -0.90 | 0.703 | 0.837 | 1.000 | 28569 | tags=59%, list=52%, signal=124% | |
3275 | REGULATION OF CYTOLYSIS | 18 | -0.32 | -0.90 | 0.573 | 0.837 | 1.000 | 29286 | tags=67%, list=54%, signal=144% | |
3276 | REGULATION OF MRNA SPLICING, VIA SPLICEOSOME | 126 | -0.26 | -0.90 | 0.579 | 0.837 | 1.000 | 21191 | tags=45%, list=39%, signal=74% | |
3277 | REGULATION OF MACROPHAGE CYTOKINE PRODUCTION | 15 | -0.33 | -0.90 | 0.571 | 0.837 | 1.000 | 14239 | tags=40%, list=26%, signal=54% | |
3278 | RESPONSE TO HYDROGEN PEROXIDE | 82 | -0.26 | -0.90 | 0.606 | 0.836 | 1.000 | 15390 | tags=37%, list=28%, signal=51% | |
3279 | NEGATIVE REGULATION OF IMMUNE EFFECTOR PROCESS | 154 | -0.25 | -0.90 | 0.622 | 0.836 | 1.000 | 21486 | tags=44%, list=39%, signal=71% | |
3280 | REGULATION OF GLUCOSE METABOLIC PROCESS | 150 | -0.22 | -0.90 | 0.704 | 0.836 | 1.000 | 23154 | tags=44%, list=42%, signal=76% | |
3281 | MORPHOGENESIS OF AN EPITHELIUM | 367 | -0.21 | -0.90 | 0.665 | 0.837 | 1.000 | 27726 | tags=51%, list=51%, signal=103% | |
3282 | MELANOSOME TRANSPORT | 24 | -0.32 | -0.90 | 0.609 | 0.836 | 1.000 | 24273 | tags=63%, list=44%, signal=112% | |
3283 | PIGMENT GRANULE TRANSPORT | 24 | -0.32 | -0.90 | 0.609 | 0.836 | 1.000 | 24273 | tags=63%, list=44%, signal=112% | |
3284 | SEQUESTERING OF EXTRACELLULAR LIGAND FROM RECEPTOR | 15 | -0.30 | -0.90 | 0.587 | 0.836 | 1.000 | 16993 | tags=40%, list=31%, signal=58% | |
3285 | MEMBRANE REPOLARIZATION DURING ACTION POTENTIAL | 9 | -0.33 | -0.90 | 0.593 | 0.836 | 1.000 | 23366 | tags=44%, list=43%, signal=78% | |
3286 | MEMBRANE REPOLARIZATION DURING CARDIAC MUSCLE CELL ACTION POTENTIAL | 9 | -0.33 | -0.90 | 0.593 | 0.836 | 1.000 | 23366 | tags=44%, list=43%, signal=78% | |
3287 | MODULATION BY HOST OF VIRAL GENOME REPLICATION | 24 | -0.30 | -0.90 | 0.601 | 0.836 | 1.000 | 33347 | tags=75%, list=61%, signal=192% | |
3288 | REGULATION OF COMPLEMENT ACTIVATION | 58 | -0.25 | -0.90 | 0.623 | 0.836 | 1.000 | 28382 | tags=60%, list=52%, signal=125% | |
3289 | PREPULSE INHIBITION | 18 | -0.32 | -0.90 | 0.589 | 0.836 | 1.000 | 18246 | tags=50%, list=33%, signal=75% | |
3290 | RESPIRATORY GASEOUS EXCHANGE | 37 | -0.29 | -0.90 | 0.610 | 0.836 | 1.000 | 28296 | tags=68%, list=52%, signal=140% | |
3291 | NEGATIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 256 | -0.23 | -0.90 | 0.716 | 0.836 | 1.000 | 29323 | tags=59%, list=54%, signal=126% | |
3292 | REGULATION OF LIPOPROTEIN PARTICLE CLEARANCE | 29 | -0.28 | -0.90 | 0.580 | 0.836 | 1.000 | 19183 | tags=41%, list=35%, signal=64% | |
3293 | CENTROMERE COMPLEX ASSEMBLY | 81 | -0.26 | -0.90 | 0.670 | 0.837 | 1.000 | 31843 | tags=72%, list=58%, signal=171% | |
3294 | REGULATION OF INTERLEUKIN-1 SECRETION | 48 | -0.28 | -0.90 | 0.648 | 0.838 | 1.000 | 22043 | tags=50%, list=40%, signal=84% | |
3295 | REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 162 | -0.23 | -0.90 | 0.652 | 0.839 | 1.000 | 20021 | tags=40%, list=37%, signal=63% | |
3296 | REGULATION OF NEURON PROJECTION DEVELOPMENT | 477 | -0.21 | -0.90 | 0.716 | 0.838 | 1.000 | 29323 | tags=57%, list=54%, signal=121% | |
3297 | REGULATION OF MYELOID CELL DIFFERENTIATION | 243 | -0.23 | -0.90 | 0.656 | 0.838 | 1.000 | 27588 | tags=51%, list=50%, signal=103% | |
3298 | BLOOD COAGULATION | 1246 | -0.21 | -0.90 | 0.603 | 0.839 | 1.000 | 28960 | tags=54%, list=53%, signal=112% | |
3299 | POSITIVE REGULATION OF PROTEIN KINASE B SIGNALING | 127 | -0.23 | -0.90 | 0.610 | 0.839 | 1.000 | 35409 | tags=69%, list=65%, signal=196% | |
3300 | CELLULAR RESPONSE TO CHOLESTEROL | 19 | -0.28 | -0.90 | 0.569 | 0.839 | 1.000 | 30257 | tags=63%, list=55%, signal=141% | |
3301 | REGULATION OF TUMOR NECROSIS FACTOR SUPERFAMILY CYTOKINE PRODUCTION | 150 | -0.25 | -0.90 | 0.602 | 0.838 | 1.000 | 15474 | tags=33%, list=28%, signal=46% | |
3302 | TEMPERATURE HOMEOSTASIS | 22 | -0.30 | -0.90 | 0.601 | 0.839 | 1.000 | 19109 | tags=45%, list=35%, signal=70% | |
3303 | NEGATIVE REGULATION OF G2/M TRANSITION OF MITOTIC CELL CYCLE | 51 | -0.26 | -0.90 | 0.604 | 0.839 | 1.000 | 14139 | tags=31%, list=26%, signal=42% | |
3304 | REGULATION OF HORMONE SECRETION | 399 | -0.21 | -0.90 | 0.662 | 0.839 | 1.000 | 22598 | tags=41%, list=41%, signal=69% | |
3305 | NEGATIVE REGULATION OF CELL DEVELOPMENT | 327 | -0.23 | -0.90 | 0.726 | 0.839 | 1.000 | 29147 | tags=57%, list=53%, signal=121% | |
3306 | MYELOID LEUKOCYTE MEDIATED IMMUNITY | 40 | -0.31 | -0.90 | 0.601 | 0.839 | 1.000 | 23476 | tags=58%, list=43%, signal=101% | |
3307 | REGULATION OF LIPID CATABOLIC PROCESS | 109 | -0.23 | -0.90 | 0.665 | 0.839 | 1.000 | 25689 | tags=50%, list=47%, signal=93% | |
3308 | REGULATION OF ACTIN FILAMENT-BASED PROCESS | 493 | -0.21 | -0.90 | 0.677 | 0.839 | 1.000 | 30177 | tags=57%, list=55%, signal=125% | |
3309 | REGULATION OF NEURON DIFFERENTIATION | 607 | -0.21 | -0.90 | 0.740 | 0.839 | 1.000 | 29323 | tags=56%, list=54%, signal=119% | |
3310 | CELLULAR CHEMICAL HOMEOSTASIS | 735 | -0.21 | -0.90 | 0.678 | 0.839 | 1.000 | 32680 | tags=61%, list=60%, signal=150% | |
3311 | NEGATIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 193 | -0.23 | -0.90 | 0.630 | 0.839 | 1.000 | 36347 | tags=75%, list=66%, signal=223% | |
3312 | REGULATION OF MITOTIC SPINDLE ASSEMBLY | 23 | -0.33 | -0.90 | 0.572 | 0.839 | 1.000 | 25722 | tags=65%, list=47%, signal=123% | |
3313 | THYMIC T CELL SELECTION | 10 | -0.41 | -0.90 | 0.598 | 0.839 | 1.000 | 16174 | tags=50%, list=30%, signal=71% | |
3314 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA PRODUCTION | 46 | -0.27 | -0.90 | 0.659 | 0.839 | 1.000 | 16993 | tags=37%, list=31%, signal=54% | |
3315 | NEGATIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 144 | -0.23 | -0.90 | 0.646 | 0.839 | 1.000 | 31967 | tags=62%, list=58%, signal=148% | |
3316 | ENDOTHELIAL CELL DIFFERENTIATION | 130 | -0.24 | -0.90 | 0.628 | 0.838 | 1.000 | 29963 | tags=59%, list=55%, signal=131% | |
3317 | FILOPODIUM ASSEMBLY | 45 | -0.24 | -0.90 | 0.633 | 0.838 | 1.000 | 26337 | tags=51%, list=48%, signal=99% | |
3318 | ENDOCARDIUM DEVELOPMENT | 18 | -0.32 | -0.90 | 0.609 | 0.838 | 1.000 | 12728 | tags=33%, list=23%, signal=43% | |
3319 | NEGATIVE REGULATION OF PROTEIN IMPORT INTO NUCLEUS | 117 | -0.23 | -0.90 | 0.620 | 0.838 | 1.000 | 30641 | tags=57%, list=56%, signal=130% | |
3320 | NEGATIVE REGULATION OF PROTEIN IMPORT | 117 | -0.23 | -0.90 | 0.620 | 0.838 | 1.000 | 30641 | tags=57%, list=56%, signal=130% | |
3321 | NON-CANONICAL WNT SIGNALING PATHWAY VIA MAPK CASCADE | 9 | -0.35 | -0.90 | 0.593 | 0.838 | 1.000 | 13690 | tags=33%, list=25%, signal=44% | |
3322 | REGULATION OF SPINDLE CHECKPOINT | 27 | -0.31 | -0.90 | 0.633 | 0.838 | 1.000 | 27848 | tags=67%, list=51%, signal=136% | |
3323 | VACUOLAR ACIDIFICATION | 28 | -0.29 | -0.90 | 0.595 | 0.838 | 1.000 | 31207 | tags=75%, list=57%, signal=175% | |
3324 | MEMBRANE ASSEMBLY | 78 | -0.25 | -0.90 | 0.630 | 0.838 | 1.000 | 21605 | tags=45%, list=40%, signal=74% | |
3325 | REGULATION OF LIPID TRANSPORT | 142 | -0.23 | -0.90 | 0.637 | 0.838 | 1.000 | 30255 | tags=57%, list=55%, signal=127% | |
3326 | REGULATION OF NEUROGENESIS | 746 | -0.21 | -0.90 | 0.754 | 0.838 | 1.000 | 28569 | tags=54%, list=52%, signal=111% | |
3327 | PHARYNGEAL SYSTEM DEVELOPMENT | 23 | -0.29 | -0.90 | 0.623 | 0.838 | 1.000 | 32149 | tags=65%, list=59%, signal=158% | |
3328 | NUCLEOBASE TRANSPORT | 12 | -0.34 | -0.90 | 0.641 | 0.838 | 1.000 | 34481 | tags=92%, list=63%, signal=248% | |
3329 | REGULATION OF PEPTIDE TRANSPORT | 416 | -0.22 | -0.90 | 0.672 | 0.839 | 1.000 | 22598 | tags=42%, list=41%, signal=71% | |
3330 | REGULATION OF KERATINOCYTE DIFFERENTIATION | 47 | -0.27 | -0.90 | 0.626 | 0.838 | 1.000 | 14790 | tags=38%, list=27%, signal=52% | |
3331 | POSITIVE REGULATION OF INTERLEUKIN-23 PRODUCTION | 10 | -0.43 | -0.90 | 0.607 | 0.838 | 1.000 | 24249 | tags=60%, list=44%, signal=108% | |
3332 | RESPONSE TO FORSKOLIN | 15 | -0.30 | -0.90 | 0.604 | 0.838 | 1.000 | 29572 | tags=53%, list=54%, signal=116% | |
3333 | CELLULAR RESPONSE TO FORSKOLIN | 15 | -0.30 | -0.90 | 0.604 | 0.838 | 1.000 | 29572 | tags=53%, list=54%, signal=116% | |
3334 | CELL AGING | 117 | -0.24 | -0.90 | 0.632 | 0.838 | 1.000 | 24508 | tags=46%, list=45%, signal=83% | |
3335 | COAGULATION | 1248 | -0.21 | -0.90 | 0.608 | 0.838 | 1.000 | 28960 | tags=54%, list=53%, signal=112% | |
3336 | TRYPTOPHAN METABOLIC PROCESS | 21 | -0.31 | -0.90 | 0.580 | 0.838 | 1.000 | 22310 | tags=52%, list=41%, signal=88% | |
3337 | PROTEIN AUTOPHOSPHORYLATION | 400 | -0.21 | -0.90 | 0.695 | 0.837 | 1.000 | 16761 | tags=34%, list=31%, signal=48% | |
3338 | NEGATIVE REGULATION OF LIPID STORAGE | 46 | -0.27 | -0.90 | 0.609 | 0.838 | 1.000 | 37449 | tags=85%, list=68%, signal=269% | |
3339 | CELL KILLING | 40 | -0.28 | -0.90 | 0.651 | 0.839 | 1.000 | 31793 | tags=70%, list=58%, signal=167% | |
3340 | POSITIVE REGULATION OF MESONEPHROS DEVELOPMENT | 35 | -0.27 | -0.90 | 0.611 | 0.839 | 1.000 | 17093 | tags=34%, list=31%, signal=50% | |
3341 | VITAMIN TRANSPORT | 45 | -0.25 | -0.90 | 0.585 | 0.838 | 1.000 | 6804 | tags=18%, list=12%, signal=20% | |
3342 | POSITIVE REGULATION OF T-HELPER CELL DIFFERENTIATION | 26 | -0.30 | -0.90 | 0.579 | 0.838 | 1.000 | 28398 | tags=54%, list=52%, signal=112% | |
3343 | POSITIVE REGULATION OF KIDNEY DEVELOPMENT | 62 | -0.25 | -0.90 | 0.609 | 0.838 | 1.000 | 17093 | tags=35%, list=31%, signal=52% | |
3344 | MUCOPOLYSACCHARIDE METABOLIC PROCESS | 242 | -0.22 | -0.90 | 0.606 | 0.838 | 1.000 | 21360 | tags=41%, list=39%, signal=67% | |
3345 | PURINE NUCLEOBASE BIOSYNTHETIC PROCESS | 13 | -0.34 | -0.90 | 0.591 | 0.838 | 1.000 | 27955 | tags=69%, list=51%, signal=142% | |
3346 | REGULATION OF SMOOTH MUSCLE CELL DIFFERENTIATION | 25 | -0.29 | -0.90 | 0.595 | 0.838 | 1.000 | 33192 | tags=72%, list=61%, signal=183% | |
3347 | LONG-CHAIN FATTY ACID BIOSYNTHETIC PROCESS | 12 | -0.36 | -0.90 | 0.557 | 0.838 | 1.000 | 32422 | tags=83%, list=59%, signal=205% | |
3348 | REGULATION OF GLUCONEOGENESIS | 40 | -0.26 | -0.90 | 0.640 | 0.838 | 1.000 | 19959 | tags=40%, list=37%, signal=63% | |
3349 | TOXIN METABOLIC PROCESS | 10 | -0.35 | -0.90 | 0.563 | 0.838 | 1.000 | 20667 | tags=50%, list=38%, signal=80% | |
3350 | APOPTOTIC CELL CLEARANCE | 42 | -0.25 | -0.90 | 0.600 | 0.837 | 1.000 | 9842 | tags=26%, list=18%, signal=32% | |
3351 | MULTICELLULAR ORGANISMAL HOMEOSTASIS | 377 | -0.21 | -0.89 | 0.662 | 0.838 | 1.000 | 21263 | tags=38%, list=39%, signal=62% | |
3352 | PYRIMIDINE RIBONUCLEOTIDE METABOLIC PROCESS | 15 | -0.34 | -0.89 | 0.588 | 0.838 | 1.000 | 19834 | tags=53%, list=36%, signal=84% | |
3353 | DEOXYRIBONUCLEOSIDE TRIPHOSPHATE METABOLIC PROCESS | 15 | -0.33 | -0.89 | 0.619 | 0.837 | 1.000 | 15508 | tags=47%, list=28%, signal=65% | |
3354 | PURINE DEOXYRIBONUCLEOSIDE TRIPHOSPHATE METABOLIC PROCESS | 15 | -0.33 | -0.89 | 0.619 | 0.837 | 1.000 | 15508 | tags=47%, list=28%, signal=65% | |
3355 | REGULATION OF DNA RECOMBINATION | 79 | -0.26 | -0.89 | 0.698 | 0.838 | 1.000 | 17701 | tags=41%, list=32%, signal=60% | |
3356 | CELLULAR RESPONSE TO CARBOHYDRATE STIMULUS | 53 | -0.27 | -0.89 | 0.685 | 0.838 | 1.000 | 22892 | tags=53%, list=42%, signal=91% | |
3357 | DETECTION OF EXTERNAL BIOTIC STIMULUS | 41 | -0.31 | -0.89 | 0.599 | 0.837 | 1.000 | 22804 | tags=51%, list=42%, signal=88% | |
3358 | REGULATION OF DOUBLE-STRAND BREAK REPAIR | 74 | -0.26 | -0.89 | 0.659 | 0.837 | 1.000 | 29055 | tags=61%, list=53%, signal=130% | |
3359 | GAMETE GENERATION | 355 | -0.20 | -0.89 | 0.706 | 0.837 | 1.000 | 21886 | tags=40%, list=40%, signal=66% | |
3360 | SPHINGOLIPID BIOSYNTHETIC PROCESS | 120 | -0.24 | -0.89 | 0.603 | 0.837 | 1.000 | 35033 | tags=73%, list=64%, signal=204% | |
3361 | EMBRYONIC HEART TUBE MORPHOGENESIS | 86 | -0.23 | -0.89 | 0.637 | 0.837 | 1.000 | 33971 | tags=69%, list=62%, signal=181% | |
3362 | REGULATION OF DENDRITE MORPHOGENESIS | 127 | -0.22 | -0.89 | 0.696 | 0.837 | 1.000 | 26643 | tags=55%, list=49%, signal=107% | |
3363 | EMBRYONIC ORGAN DEVELOPMENT | 307 | -0.20 | -0.89 | 0.710 | 0.837 | 1.000 | 30616 | tags=55%, list=56%, signal=125% | |
3364 | POSITIVE REGULATION OF HOMEOSTATIC PROCESS | 350 | -0.22 | -0.89 | 0.719 | 0.837 | 1.000 | 16443 | tags=33%, list=30%, signal=46% | |
3365 | RENAL SYSTEM PROCESS INVOLVED IN REGULATION OF BLOOD VOLUME | 25 | -0.27 | -0.89 | 0.587 | 0.837 | 1.000 | 28804 | tags=68%, list=53%, signal=144% | |
3366 | REGULATION OF DNA-TEMPLATED TRANSCRIPTION, INITIATION | 53 | -0.26 | -0.89 | 0.653 | 0.837 | 1.000 | 34524 | tags=75%, list=63%, signal=205% | |
3367 | OLIGOSACCHARIDE METABOLIC PROCESS | 66 | -0.23 | -0.89 | 0.680 | 0.837 | 1.000 | 13468 | tags=29%, list=25%, signal=38% | |
3368 | EXOCRINE SYSTEM DEVELOPMENT | 30 | -0.28 | -0.89 | 0.589 | 0.837 | 1.000 | 21813 | tags=43%, list=40%, signal=72% | |
3369 | REGULATION OF MESENCHYMAL CELL PROLIFERATION | 48 | -0.27 | -0.89 | 0.599 | 0.838 | 1.000 | 16824 | tags=38%, list=31%, signal=54% | |
3370 | PHOSPHATIDYLINOSITOL 3-KINASE SIGNALING | 64 | -0.26 | -0.89 | 0.657 | 0.837 | 1.000 | 31126 | tags=69%, list=57%, signal=159% | |
3371 | CELLULAR RESPONSE TO LIPID | 454 | -0.22 | -0.89 | 0.675 | 0.838 | 1.000 | 20708 | tags=38%, list=38%, signal=60% | |
3372 | POSITIVE REGULATION OF APOPTOTIC CELL CLEARANCE | 8 | -0.39 | -0.89 | 0.620 | 0.838 | 1.000 | 21192 | tags=63%, list=39%, signal=102% | |
3373 | POSITIVE REGULATION OF ACTIN FILAMENT BUNDLE ASSEMBLY | 91 | -0.25 | -0.89 | 0.616 | 0.837 | 1.000 | 33766 | tags=74%, list=62%, signal=192% | |
3374 | PERIPHERAL NERVOUS SYSTEM NEURON DIFFERENTIATION | 26 | -0.29 | -0.89 | 0.622 | 0.838 | 1.000 | 27891 | tags=50%, list=51%, signal=102% | |
3375 | PERIPHERAL NERVOUS SYSTEM NEURON DEVELOPMENT | 26 | -0.29 | -0.89 | 0.622 | 0.837 | 1.000 | 27891 | tags=50%, list=51%, signal=102% | |
3376 | TRYPTOPHAN CATABOLIC PROCESS | 19 | -0.32 | -0.89 | 0.578 | 0.837 | 1.000 | 22310 | tags=53%, list=41%, signal=89% | |
3377 | INDOLE-CONTAINING COMPOUND CATABOLIC PROCESS | 19 | -0.32 | -0.89 | 0.578 | 0.837 | 1.000 | 22310 | tags=53%, list=41%, signal=89% | |
3378 | INDOLALKYLAMINE CATABOLIC PROCESS | 19 | -0.32 | -0.89 | 0.578 | 0.837 | 1.000 | 22310 | tags=53%, list=41%, signal=89% | |
3379 | ORGANIC ANION TRANSPORT | 586 | -0.21 | -0.89 | 0.691 | 0.837 | 1.000 | 25822 | tags=48%, list=47%, signal=90% | |
3380 | REGULATION OF GLYCOLYTIC PROCESS | 61 | -0.26 | -0.89 | 0.670 | 0.837 | 1.000 | 25156 | tags=54%, list=46%, signal=100% | |
3381 | NONMOTILE PRIMARY CILIUM ASSEMBLY | 40 | -0.29 | -0.89 | 0.585 | 0.837 | 1.000 | 34624 | tags=80%, list=63%, signal=218% | |
3382 | REGULATION OF REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 92 | -0.25 | -0.89 | 0.658 | 0.837 | 1.000 | 14129 | tags=30%, list=26%, signal=41% | |
3383 | NEGATIVE REGULATION OF NEUROGENESIS | 234 | -0.23 | -0.89 | 0.719 | 0.837 | 1.000 | 29005 | tags=58%, list=53%, signal=123% | |
3384 | HIPPOCAMPUS DEVELOPMENT | 46 | -0.28 | -0.89 | 0.622 | 0.837 | 1.000 | 31514 | tags=74%, list=58%, signal=174% | |
3385 | CELLULAR METAL ION HOMEOSTASIS | 595 | -0.21 | -0.89 | 0.677 | 0.837 | 1.000 | 19611 | tags=36%, list=36%, signal=56% | |
3386 | ADENINE TRANSPORT | 6 | -0.43 | -0.89 | 0.600 | 0.837 | 1.000 | 18588 | tags=67%, list=34%, signal=101% | |
3387 | NEGATIVE REGULATION OF AXONOGENESIS | 62 | -0.26 | -0.89 | 0.678 | 0.837 | 1.000 | 29323 | tags=65%, list=54%, signal=139% | |
3388 | REGULATION OF DENDRITIC SPINE DEVELOPMENT | 94 | -0.24 | -0.89 | 0.699 | 0.837 | 1.000 | 29852 | tags=64%, list=55%, signal=140% | |
3389 | STEROID METABOLIC PROCESS | 345 | -0.21 | -0.89 | 0.674 | 0.837 | 1.000 | 32064 | tags=63%, list=59%, signal=150% | |
3390 | CHEMOSENSORY BEHAVIOR | 14 | -0.35 | -0.89 | 0.617 | 0.838 | 1.000 | 895 | tags=14%, list=2%, signal=15% | |
3391 | MEMBRANE DOCKING | 60 | -0.26 | -0.89 | 0.687 | 0.838 | 1.000 | 27789 | tags=62%, list=51%, signal=125% | |
3392 | DEFENSE RESPONSE TO OTHER ORGANISM | 550 | -0.22 | -0.89 | 0.658 | 0.838 | 1.000 | 25181 | tags=48%, list=46%, signal=88% | |
3393 | POSITIVE REGULATION OF LIPID TRANSPORT | 61 | -0.25 | -0.89 | 0.662 | 0.838 | 1.000 | 29822 | tags=57%, list=55%, signal=126% | |
3394 | RESPONSE TO ESTRADIOL | 76 | -0.22 | -0.89 | 0.651 | 0.838 | 1.000 | 19816 | tags=36%, list=36%, signal=56% | |
3395 | DETERMINATION OF LEFT/RIGHT SYMMETRY | 119 | -0.23 | -0.89 | 0.610 | 0.839 | 1.000 | 33971 | tags=69%, list=62%, signal=182% | |
3396 | AORTIC VALVE DEVELOPMENT | 8 | -0.40 | -0.89 | 0.613 | 0.839 | 1.000 | 12785 | tags=38%, list=23%, signal=49% | |
3397 | AORTIC VALVE MORPHOGENESIS | 8 | -0.40 | -0.89 | 0.613 | 0.838 | 1.000 | 12785 | tags=38%, list=23%, signal=49% | |
3398 | SINGLE STRAND BREAK REPAIR | 12 | -0.34 | -0.89 | 0.636 | 0.838 | 1.000 | 25567 | tags=67%, list=47%, signal=125% | |
3399 | REGULATION OF BICELLULAR TIGHT JUNCTION ASSEMBLY | 22 | -0.29 | -0.89 | 0.592 | 0.839 | 1.000 | 13664 | tags=36%, list=25%, signal=48% | |
3400 | POSITIVE REGULATION OF FOCAL ADHESION ASSEMBLY | 37 | -0.27 | -0.89 | 0.606 | 0.839 | 1.000 | 29501 | tags=65%, list=54%, signal=141% | |
3401 | PHOSPHATIDYLETHANOLAMINE METABOLIC PROCESS | 34 | -0.29 | -0.89 | 0.582 | 0.839 | 1.000 | 27597 | tags=65%, list=50%, signal=131% | |
3402 | REGULATION OF FOCAL ADHESION ASSEMBLY | 126 | -0.23 | -0.89 | 0.660 | 0.839 | 1.000 | 30488 | tags=61%, list=56%, signal=138% | |
3403 | REGULATION OF CELL-SUBSTRATE JUNCTION ASSEMBLY | 126 | -0.23 | -0.89 | 0.660 | 0.839 | 1.000 | 30488 | tags=61%, list=56%, signal=138% | |
3404 | CELLULAR RESPONSE TO REACTIVE OXYGEN SPECIES | 125 | -0.23 | -0.89 | 0.683 | 0.839 | 1.000 | 22875 | tags=44%, list=42%, signal=75% | |
3405 | HEART LOOPING | 78 | -0.23 | -0.89 | 0.629 | 0.839 | 1.000 | 33971 | tags=69%, list=62%, signal=183% | |
3406 | REGULATION OF OXIDATIVE STRESS-INDUCED INTRINSIC APOPTOTIC SIGNALING PATHWAY | 55 | -0.29 | -0.89 | 0.638 | 0.838 | 1.000 | 19983 | tags=49%, list=37%, signal=77% | |
3407 | ASTRAL MICROTUBULE ORGANIZATION | 23 | -0.33 | -0.89 | 0.600 | 0.840 | 1.000 | 20317 | tags=52%, list=37%, signal=83% | |
3408 | REGULATION OF CHOLESTEROL STORAGE | 40 | -0.30 | -0.89 | 0.607 | 0.840 | 1.000 | 3196 | tags=20%, list=6%, signal=21% | |
3409 | REGULATION OF ADRENERGIC RECEPTOR SIGNALING PATHWAY | 13 | -0.28 | -0.89 | 0.664 | 0.840 | 1.000 | 11362 | tags=31%, list=21%, signal=39% | |
3410 | ANDROGEN BIOSYNTHETIC PROCESS | 22 | -0.29 | -0.89 | 0.650 | 0.840 | 1.000 | 18704 | tags=41%, list=34%, signal=62% | |
3411 | DETERMINATION OF HEART LEFT/RIGHT ASYMMETRY | 81 | -0.24 | -0.89 | 0.622 | 0.840 | 1.000 | 36275 | tags=75%, list=66%, signal=223% | |
3412 | AMINO SUGAR METABOLIC PROCESS | 54 | -0.26 | -0.89 | 0.626 | 0.840 | 1.000 | 37306 | tags=85%, list=68%, signal=268% | |
3413 | POSITIVE REGULATION OF CELL JUNCTION ASSEMBLY | 46 | -0.26 | -0.89 | 0.603 | 0.840 | 1.000 | 9923 | tags=28%, list=18%, signal=34% | |
3414 | NEGATIVE REGULATION OF MICROTUBULE POLYMERIZATION OR DEPOLYMERIZATION | 61 | -0.24 | -0.89 | 0.660 | 0.840 | 1.000 | 29029 | tags=59%, list=53%, signal=126% | |
3415 | NEGATIVE REGULATION OF ACTIVATED T CELL PROLIFERATION | 17 | -0.31 | -0.89 | 0.606 | 0.840 | 1.000 | 33777 | tags=76%, list=62%, signal=200% | |
3416 | LONG-CHAIN FATTY ACID TRANSPORT | 69 | -0.25 | -0.89 | 0.615 | 0.841 | 1.000 | 26115 | tags=58%, list=48%, signal=111% | |
3417 | EMBRYONIC AXIS SPECIFICATION | 41 | -0.28 | -0.89 | 0.592 | 0.841 | 1.000 | 18797 | tags=37%, list=34%, signal=56% | |
3418 | POSITIVE REGULATION OF ADHERENS JUNCTION ORGANIZATION | 39 | -0.26 | -0.89 | 0.624 | 0.840 | 1.000 | 29501 | tags=64%, list=54%, signal=139% | |
3419 | LONG-CHAIN FATTY ACID CATABOLIC PROCESS | 8 | -0.37 | -0.89 | 0.584 | 0.841 | 1.000 | 28804 | tags=75%, list=53%, signal=158% | |
3420 | POSITIVE REGULATION OF CILIUM ASSEMBLY | 18 | -0.29 | -0.89 | 0.653 | 0.841 | 1.000 | 26637 | tags=61%, list=49%, signal=119% | |
3421 | REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR SIGNALING PATHWAY | 23 | -0.31 | -0.89 | 0.584 | 0.841 | 1.000 | 7500 | tags=26%, list=14%, signal=30% | |
3422 | POSITIVE REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 69 | -0.23 | -0.89 | 0.634 | 0.841 | 1.000 | 22664 | tags=42%, list=41%, signal=72% | |
3423 | REGULATION OF HISTONE DEACETYLATION | 53 | -0.26 | -0.89 | 0.656 | 0.841 | 1.000 | 25077 | tags=55%, list=46%, signal=101% | |
3424 | MUCOSAL IMMUNE RESPONSE | 34 | -0.26 | -0.88 | 0.612 | 0.842 | 1.000 | 7301 | tags=24%, list=13%, signal=27% | |
3425 | REGULATION OF CELL SIZE | 169 | -0.22 | -0.88 | 0.685 | 0.843 | 1.000 | 28543 | tags=53%, list=52%, signal=111% | |
3426 | ACTIVATION OF GTPASE ACTIVITY | 72 | -0.22 | -0.88 | 0.673 | 0.844 | 1.000 | 25858 | tags=47%, list=47%, signal=89% | |
3427 | INTERLEUKIN-4-MEDIATED SIGNALING PATHWAY | 8 | -0.38 | -0.88 | 0.611 | 0.844 | 1.000 | 30466 | tags=75%, list=56%, signal=169% | |
3428 | NEGATIVE REGULATION OF LIPID CATABOLIC PROCESS | 39 | -0.27 | -0.88 | 0.619 | 0.844 | 1.000 | 29616 | tags=62%, list=54%, signal=134% | |
3429 | REGULATION OF GLUCOSE TRANSPORT | 187 | -0.22 | -0.88 | 0.690 | 0.844 | 1.000 | 29175 | tags=56%, list=53%, signal=120% | |
3430 | RECEPTOR-MEDIATED VIRION ATTACHMENT TO HOST CELL | 10 | -0.38 | -0.88 | 0.642 | 0.844 | 1.000 | 9404 | tags=40%, list=17%, signal=48% | |
3431 | ENTRY INTO HOST CELL | 79 | -0.25 | -0.88 | 0.627 | 0.844 | 1.000 | 33564 | tags=76%, list=61%, signal=196% | |
3432 | ENTRY INTO HOST | 79 | -0.25 | -0.88 | 0.627 | 0.844 | 1.000 | 33564 | tags=76%, list=61%, signal=196% | |
3433 | ENTRY INTO CELL OF OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 79 | -0.25 | -0.88 | 0.627 | 0.844 | 1.000 | 33564 | tags=76%, list=61%, signal=196% | |
3434 | ENTRY INTO OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 79 | -0.25 | -0.88 | 0.627 | 0.843 | 1.000 | 33564 | tags=76%, list=61%, signal=196% | |
3435 | MOVEMENT IN HOST ENVIRONMENT | 79 | -0.25 | -0.88 | 0.627 | 0.843 | 1.000 | 33564 | tags=76%, list=61%, signal=196% | |
3436 | MOVEMENT IN ENVIRONMENT OF OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 79 | -0.25 | -0.88 | 0.627 | 0.843 | 1.000 | 33564 | tags=76%, list=61%, signal=196% | |
3437 | CELL COMMUNICATION BY ELECTRICAL COUPLING INVOLVED IN CARDIAC CONDUCTION | 30 | -0.28 | -0.88 | 0.631 | 0.843 | 1.000 | 22870 | tags=43%, list=42%, signal=74% | |
3438 | MULTICELLULAR ORGANISM REPRODUCTION | 460 | -0.20 | -0.88 | 0.751 | 0.843 | 1.000 | 21886 | tags=39%, list=40%, signal=64% | |
3439 | SNRNA TRANSCRIPTION | 19 | -0.32 | -0.88 | 0.630 | 0.843 | 1.000 | 30021 | tags=74%, list=55%, signal=163% | |
3440 | REGULATION OF CELL JUNCTION ASSEMBLY | 166 | -0.22 | -0.88 | 0.665 | 0.843 | 1.000 | 30488 | tags=60%, list=56%, signal=136% | |
3441 | REGULATION OF APOPTOTIC CELL CLEARANCE | 10 | -0.35 | -0.88 | 0.619 | 0.843 | 1.000 | 29938 | tags=80%, list=55%, signal=177% | |
3442 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER INVOLVED IN HEART DEVELOPMENT | 23 | -0.28 | -0.88 | 0.600 | 0.843 | 1.000 | 6485 | tags=22%, list=12%, signal=25% | |
3443 | MEMORY | 53 | -0.23 | -0.88 | 0.645 | 0.843 | 1.000 | 11397 | tags=25%, list=21%, signal=31% | |
3444 | PROTEIN DEGLYCOSYLATION | 27 | -0.31 | -0.88 | 0.612 | 0.843 | 1.000 | 33270 | tags=81%, list=61%, signal=208% | |
3445 | REGULATION OF CILIUM MOVEMENT | 22 | -0.33 | -0.88 | 0.588 | 0.843 | 1.000 | 33316 | tags=86%, list=61%, signal=221% | |
3446 | PYRIMIDINE RIBONUCLEOTIDE BIOSYNTHETIC PROCESS | 10 | -0.37 | -0.88 | 0.584 | 0.843 | 1.000 | 18592 | tags=50%, list=34%, signal=76% | |
3447 | GLYCOSAMINOGLYCAN METABOLIC PROCESS | 318 | -0.21 | -0.88 | 0.635 | 0.843 | 1.000 | 21375 | tags=40%, list=39%, signal=66% | |
3448 | FLAVIN-CONTAINING COMPOUND METABOLIC PROCESS | 13 | -0.32 | -0.88 | 0.631 | 0.843 | 1.000 | 5263 | tags=23%, list=10%, signal=26% | |
3449 | GLYCOSYLCERAMIDE METABOLIC PROCESS | 15 | -0.33 | -0.88 | 0.641 | 0.844 | 1.000 | 25665 | tags=67%, list=47%, signal=126% | |
3450 | MESENCHYMAL CELL DEVELOPMENT | 139 | -0.21 | -0.88 | 0.681 | 0.844 | 1.000 | 25277 | tags=45%, list=46%, signal=84% | |
3451 | POSITIVE REGULATION OF NEURON APOPTOTIC PROCESS | 58 | -0.27 | -0.88 | 0.666 | 0.844 | 1.000 | 26388 | tags=59%, list=48%, signal=113% | |
3452 | MACROPHAGE CHEMOTAXIS | 17 | -0.36 | -0.88 | 0.621 | 0.843 | 1.000 | 11326 | tags=29%, list=21%, signal=37% | |
3453 | REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 430 | -0.21 | -0.88 | 0.703 | 0.844 | 1.000 | 17100 | tags=33%, list=31%, signal=48% | |
3454 | POSITIVE REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 414 | -0.22 | -0.88 | 0.692 | 0.844 | 1.000 | 15479 | tags=31%, list=28%, signal=43% | |
3455 | CELL-CELL JUNCTION MAINTENANCE | 7 | -0.39 | -0.88 | 0.619 | 0.844 | 1.000 | 33358 | tags=100%, list=61%, signal=256% | |
3456 | CILIUM MORPHOGENESIS | 366 | -0.26 | -0.88 | 0.603 | 0.844 | 1.000 | 28636 | tags=62%, list=52%, signal=130% | |
3457 | CARBOHYDRATE DERIVATIVE CATABOLIC PROCESS | 316 | -0.21 | -0.88 | 0.667 | 0.845 | 1.000 | 20622 | tags=39%, list=38%, signal=63% | |
3458 | NEGATIVE REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL PROLIFERATION INVOLVED IN SPROUTING ANGIOGENESIS | 2 | -0.50 | -0.88 | 0.647 | 0.845 | 1.000 | 10215 | tags=50%, list=19%, signal=61% | |
3459 | HETEROTYPIC CELL-CELL ADHESION | 58 | -0.26 | -0.88 | 0.659 | 0.845 | 1.000 | 33261 | tags=72%, list=61%, signal=185% | |
3460 | ISOPRENOID METABOLIC PROCESS | 191 | -0.21 | -0.88 | 0.650 | 0.845 | 1.000 | 33967 | tags=63%, list=62%, signal=167% | |
3461 | POSITIVE REGULATION OF FATTY ACID OXIDATION | 34 | -0.27 | -0.88 | 0.677 | 0.845 | 1.000 | 25689 | tags=53%, list=47%, signal=100% | |
3462 | CELL PROLIFERATION IN FOREBRAIN | 35 | -0.28 | -0.88 | 0.640 | 0.845 | 1.000 | 29991 | tags=66%, list=55%, signal=145% | |
3463 | REGULATION OF ICOSANOID SECRETION | 24 | -0.31 | -0.88 | 0.634 | 0.845 | 1.000 | 28880 | tags=67%, list=53%, signal=141% | |
3464 | BETA-AMYLOID METABOLIC PROCESS | 16 | -0.30 | -0.88 | 0.630 | 0.845 | 1.000 | 24255 | tags=50%, list=44%, signal=90% | |
3465 | AMINE CATABOLIC PROCESS | 26 | -0.28 | -0.88 | 0.621 | 0.845 | 1.000 | 17350 | tags=38%, list=32%, signal=56% | |
3466 | CELLULAR BIOGENIC AMINE CATABOLIC PROCESS | 26 | -0.28 | -0.88 | 0.621 | 0.845 | 1.000 | 17350 | tags=38%, list=32%, signal=56% | |
3467 | HISTONE EXCHANGE | 89 | -0.25 | -0.88 | 0.692 | 0.845 | 1.000 | 34810 | tags=75%, list=64%, signal=207% | |
3468 | POSITIVE REGULATION OF NATURAL KILLER CELL ACTIVATION | 18 | -0.31 | -0.88 | 0.653 | 0.845 | 1.000 | 31852 | tags=78%, list=58%, signal=186% | |
3469 | CELLULAR RESPONSE TO PROSTAGLANDIN STIMULUS | 32 | -0.29 | -0.88 | 0.635 | 0.845 | 1.000 | 13452 | tags=34%, list=25%, signal=46% | |
3470 | RUFFLE ORGANIZATION | 39 | -0.28 | -0.88 | 0.621 | 0.845 | 1.000 | 18367 | tags=41%, list=34%, signal=62% | |
3471 | CENP-A CONTAINING NUCLEOSOME ASSEMBLY | 70 | -0.26 | -0.88 | 0.709 | 0.845 | 1.000 | 35715 | tags=80%, list=65%, signal=230% | |
3472 | CENP-A CONTAINING CHROMATIN ORGANIZATION | 70 | -0.26 | -0.88 | 0.709 | 0.845 | 1.000 | 35715 | tags=80%, list=65%, signal=230% | |
3473 | SECRETION BY CELL | 683 | -0.22 | -0.88 | 0.663 | 0.845 | 1.000 | 23288 | tags=44%, list=43%, signal=76% | |
3474 | REGULATION OF MYOTUBE DIFFERENTIATION | 87 | -0.25 | -0.88 | 0.639 | 0.845 | 1.000 | 9548 | tags=24%, list=17%, signal=29% | |
3475 | NUCLEOBASE BIOSYNTHETIC PROCESS | 15 | -0.32 | -0.88 | 0.613 | 0.845 | 1.000 | 27955 | tags=67%, list=51%, signal=136% | |
3476 | REGULATION OF NOTCH SIGNALING PATHWAY | 89 | -0.22 | -0.88 | 0.674 | 0.845 | 1.000 | 26808 | tags=52%, list=49%, signal=101% | |
3477 | SISTER CHROMATID COHESION | 70 | -0.26 | -0.88 | 0.611 | 0.845 | 1.000 | 28394 | tags=61%, list=52%, signal=128% | |
3478 | DICARBOXYLIC ACID TRANSPORT | 103 | -0.22 | -0.88 | 0.683 | 0.845 | 1.000 | 17082 | tags=33%, list=31%, signal=48% | |
3479 | AMINOGLYCAN METABOLIC PROCESS | 321 | -0.21 | -0.88 | 0.645 | 0.845 | 1.000 | 21375 | tags=40%, list=39%, signal=65% | |
3480 | NOSE DEVELOPMENT | 14 | -0.33 | -0.88 | 0.648 | 0.845 | 1.000 | 16174 | tags=43%, list=30%, signal=61% | |
3481 | REGULATION OF CATENIN IMPORT INTO NUCLEUS | 51 | -0.25 | -0.88 | 0.586 | 0.845 | 1.000 | 29055 | tags=53%, list=53%, signal=113% | |
3482 | REGULATION OF ORGAN MORPHOGENESIS | 194 | -0.20 | -0.88 | 0.688 | 0.845 | 1.000 | 23725 | tags=42%, list=43%, signal=74% | |
3483 | CENTRIOLE REPLICATION | 38 | -0.25 | -0.88 | 0.668 | 0.845 | 1.000 | 32637 | tags=68%, list=60%, signal=170% | |
3484 | POSITIVE REGULATION OF PROTEIN COMPLEX DISASSEMBLY | 47 | -0.26 | -0.88 | 0.706 | 0.845 | 1.000 | 32761 | tags=68%, list=60%, signal=170% | |
3485 | NEGATIVE REGULATION OF FATTY ACID TRANSPORT | 25 | -0.29 | -0.88 | 0.610 | 0.845 | 1.000 | 11110 | tags=32%, list=20%, signal=40% | |
3486 | REGULATION OF PROTEIN EXIT FROM ENDOPLASMIC RETICULUM | 46 | -0.27 | -0.88 | 0.623 | 0.845 | 1.000 | 15093 | tags=39%, list=28%, signal=54% | |
3487 | CELLULAR CATION HOMEOSTASIS | 649 | -0.21 | -0.88 | 0.718 | 0.845 | 1.000 | 32671 | tags=60%, list=60%, signal=148% | |
3488 | RESPONSE TO MOLECULE OF BACTERIAL ORIGIN | 261 | -0.25 | -0.88 | 0.684 | 0.846 | 1.000 | 21390 | tags=43%, list=39%, signal=70% | |
3489 | NEGATIVE REGULATION OF JUN KINASE ACTIVITY | 25 | -0.32 | -0.88 | 0.603 | 0.846 | 1.000 | 20589 | tags=52%, list=38%, signal=83% | |
3490 | NEUROEPITHELIAL CELL DIFFERENTIATION | 34 | -0.25 | -0.88 | 0.663 | 0.846 | 1.000 | 27588 | tags=56%, list=50%, signal=113% | |
3491 | REGULATION OF CHEMOKINE (C-C MOTIF) LIGAND 5 PRODUCTION | 16 | -0.33 | -0.88 | 0.590 | 0.846 | 1.000 | 5565 | tags=25%, list=10%, signal=28% | |
3492 | HEART GROWTH | 35 | -0.26 | -0.88 | 0.633 | 0.846 | 1.000 | 26563 | tags=54%, list=49%, signal=106% | |
3493 | CELLULAR HOMEOSTASIS | 876 | -0.20 | -0.88 | 0.754 | 0.846 | 1.000 | 29089 | tags=54%, list=53%, signal=113% | |
3494 | MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION | 10 | -0.37 | -0.88 | 0.600 | 0.846 | 1.000 | 24805 | tags=70%, list=45%, signal=128% | |
3495 | PLATELET DEGRANULATION | 236 | -0.23 | -0.88 | 0.621 | 0.846 | 1.000 | 21592 | tags=43%, list=39%, signal=70% | |
3496 | NEPHRIC DUCT DEVELOPMENT | 19 | -0.30 | -0.87 | 0.618 | 0.846 | 1.000 | 14059 | tags=32%, list=26%, signal=42% | |
3497 | ORGANELLE INHERITANCE | 21 | -0.31 | -0.87 | 0.646 | 0.846 | 1.000 | 16089 | tags=43%, list=29%, signal=61% | |
3498 | GOLGI INHERITANCE | 21 | -0.31 | -0.87 | 0.646 | 0.846 | 1.000 | 16089 | tags=43%, list=29%, signal=61% | |
3499 | REGULATION OF RNA SPLICING | 226 | -0.25 | -0.87 | 0.622 | 0.846 | 1.000 | 24463 | tags=50%, list=45%, signal=90% | |
3500 | CELLULAR RESPONSE TO VIRUS | 22 | -0.27 | -0.87 | 0.606 | 0.846 | 1.000 | 3287 | tags=18%, list=6%, signal=19% | |
3501 | BILE ACID AND BILE SALT TRANSPORT | 51 | -0.26 | -0.87 | 0.675 | 0.846 | 1.000 | 31508 | tags=65%, list=58%, signal=153% | |
3502 | CHROMATIN REMODELING AT CENTROMERE | 78 | -0.26 | -0.87 | 0.704 | 0.846 | 1.000 | 31843 | tags=71%, list=58%, signal=169% | |
3503 | MEIOTIC CELL CYCLE | 138 | -0.21 | -0.87 | 0.702 | 0.845 | 1.000 | 10619 | tags=22%, list=19%, signal=27% | |
3504 | MEIOTIC CELL CYCLE PROCESS | 138 | -0.21 | -0.87 | 0.702 | 0.845 | 1.000 | 10619 | tags=22%, list=19%, signal=27% | |
3505 | REGULATION OF HELICASE ACTIVITY | 18 | -0.34 | -0.87 | 0.589 | 0.845 | 1.000 | 17563 | tags=50%, list=32%, signal=74% | |
3506 | NEUTROPHIL HOMEOSTASIS | 11 | -0.39 | -0.87 | 0.614 | 0.845 | 1.000 | 22653 | tags=55%, list=41%, signal=93% | |
3507 | POSITIVE REGULATION OF DENDRITIC SPINE DEVELOPMENT | 44 | -0.25 | -0.87 | 0.669 | 0.845 | 1.000 | 16486 | tags=39%, list=30%, signal=55% | |
3508 | POSITIVE REGULATION OF STRIATED MUSCLE CONTRACTION | 18 | -0.32 | -0.87 | 0.610 | 0.845 | 1.000 | 15903 | tags=33%, list=29%, signal=47% | |
3509 | POSITIVE REGULATION OF RYANODINE-SENSITIVE CALCIUM-RELEASE CHANNEL ACTIVITY | 30 | -0.27 | -0.87 | 0.608 | 0.845 | 1.000 | 22210 | tags=50%, list=41%, signal=84% | |
3510 | SYNAPTIC VESICLE ENDOCYTOSIS | 29 | -0.28 | -0.87 | 0.670 | 0.845 | 1.000 | 16426 | tags=38%, list=30%, signal=54% | |
3511 | REGULATION OF CELL-MATRIX ADHESION | 213 | -0.22 | -0.87 | 0.683 | 0.845 | 1.000 | 30488 | tags=60%, list=56%, signal=135% | |
3512 | DNA REPLICATION-DEPENDENT NUCLEOSOME ASSEMBLY | 42 | -0.27 | -0.87 | 0.670 | 0.845 | 1.000 | 28239 | tags=62%, list=52%, signal=128% | |
3513 | DNA REPLICATION-DEPENDENT NUCLEOSOME ORGANIZATION | 42 | -0.27 | -0.87 | 0.670 | 0.844 | 1.000 | 28239 | tags=62%, list=52%, signal=128% | |
3514 | PHYSIOLOGICAL MUSCLE HYPERTROPHY | 17 | -0.32 | -0.87 | 0.600 | 0.844 | 1.000 | 26563 | tags=65%, list=49%, signal=126% | |
3515 | PHYSIOLOGICAL CARDIAC MUSCLE HYPERTROPHY | 17 | -0.32 | -0.87 | 0.600 | 0.844 | 1.000 | 26563 | tags=65%, list=49%, signal=126% | |
3516 | CELL GROWTH INVOLVED IN CARDIAC MUSCLE CELL DEVELOPMENT | 17 | -0.32 | -0.87 | 0.600 | 0.844 | 1.000 | 26563 | tags=65%, list=49%, signal=126% | |
3517 | LABYRINTHINE LAYER DEVELOPMENT | 23 | -0.28 | -0.87 | 0.618 | 0.844 | 1.000 | 25051 | tags=57%, list=46%, signal=104% | |
3518 | REGULATION OF HEMOPOIESIS | 403 | -0.21 | -0.87 | 0.717 | 0.844 | 1.000 | 27588 | tags=50%, list=50%, signal=100% | |
3519 | POSITIVE REGULATION OF EXTRACELLULAR MATRIX ASSEMBLY | 25 | -0.27 | -0.87 | 0.607 | 0.844 | 1.000 | 18901 | tags=44%, list=35%, signal=67% | |
3520 | REGULATION OF HISTONE H3-K4 METHYLATION | 51 | -0.29 | -0.87 | 0.655 | 0.844 | 1.000 | 28774 | tags=67%, list=53%, signal=141% | |
3521 | INORGANIC ION HOMEOSTASIS | 764 | -0.20 | -0.87 | 0.737 | 0.844 | 1.000 | 32530 | tags=60%, list=59%, signal=146% | |
3522 | SIGNAL PEPTIDE PROCESSING | 18 | -0.30 | -0.87 | 0.632 | 0.845 | 1.000 | 27317 | tags=67%, list=50%, signal=133% | |
3523 | REGULATION OF INTERLEUKIN-1 BETA SECRETION | 39 | -0.28 | -0.87 | 0.667 | 0.845 | 1.000 | 14684 | tags=36%, list=27%, signal=49% | |
3524 | CELL-SUBSTRATE ADHESION | 265 | -0.21 | -0.87 | 0.707 | 0.845 | 1.000 | 35599 | tags=68%, list=65%, signal=194% | |
3525 | TOR SIGNALING | 45 | -0.26 | -0.87 | 0.661 | 0.845 | 1.000 | 10514 | tags=29%, list=19%, signal=36% | |
3526 | CELLULAR RESPONSE TO GAMMA RADIATION | 22 | -0.29 | -0.87 | 0.680 | 0.845 | 1.000 | 16967 | tags=41%, list=31%, signal=59% | |
3527 | NEGATIVE REGULATION OF PROTEIN KINASE ACTIVITY BY REGULATION OF PROTEIN PHOSPHORYLATION | 17 | -0.28 | -0.87 | 0.617 | 0.845 | 1.000 | 8600 | tags=29%, list=16%, signal=35% | |
3528 | ION HOMEOSTASIS | 825 | -0.20 | -0.87 | 0.718 | 0.845 | 1.000 | 19611 | tags=36%, list=36%, signal=55% | |
3529 | GERM CELL DEVELOPMENT | 108 | -0.20 | -0.87 | 0.682 | 0.845 | 1.000 | 21263 | tags=38%, list=39%, signal=62% | |
3530 | G-PROTEIN COUPLED GLUTAMATE RECEPTOR SIGNALING PATHWAY | 25 | -0.27 | -0.87 | 0.612 | 0.845 | 1.000 | 9023 | tags=20%, list=17%, signal=24% | |
3531 | NEGATIVE REGULATION OF T CELL PROLIFERATION | 49 | -0.26 | -0.87 | 0.643 | 0.845 | 1.000 | 24197 | tags=49%, list=44%, signal=88% | |
3532 | REGULATION OF LOW-DENSITY LIPOPROTEIN PARTICLE RECEPTOR BIOSYNTHETIC PROCESS | 15 | -0.31 | -0.87 | 0.641 | 0.845 | 1.000 | 7462 | tags=27%, list=14%, signal=31% | |
3533 | FATTY ACID HOMEOSTASIS | 21 | -0.30 | -0.87 | 0.650 | 0.845 | 1.000 | 26332 | tags=62%, list=48%, signal=119% | |
3534 | CELLULAR ION HOMEOSTASIS | 667 | -0.21 | -0.87 | 0.725 | 0.845 | 1.000 | 32680 | tags=60%, list=60%, signal=148% | |
3535 | REGULATION OF EPITHELIAL CELL PROLIFERATION | 415 | -0.20 | -0.87 | 0.707 | 0.846 | 1.000 | 36030 | tags=68%, list=66%, signal=199% | |
3536 | REGULATION OF BASEMENT MEMBRANE ASSEMBLY INVOLVED IN EMBRYONIC BODY MORPHOGENESIS | 18 | -0.29 | -0.87 | 0.657 | 0.847 | 1.000 | 21765 | tags=50%, list=40%, signal=83% | |
3537 | POSITIVE REGULATION OF BASEMENT MEMBRANE ASSEMBLY INVOLVED IN EMBRYONIC BODY MORPHOGENESIS | 18 | -0.29 | -0.87 | 0.657 | 0.847 | 1.000 | 21765 | tags=50%, list=40%, signal=83% | |
3538 | NEGATIVE REGULATION OF CYTOSKELETON ORGANIZATION | 183 | -0.22 | -0.87 | 0.735 | 0.846 | 1.000 | 32057 | tags=63%, list=59%, signal=151% | |
3539 | CANONICAL WNT SIGNALING PATHWAY | 129 | -0.22 | -0.87 | 0.701 | 0.846 | 1.000 | 19317 | tags=40%, list=35%, signal=61% | |
3540 | POSITIVE REGULATION OF GLYCOGEN METABOLIC PROCESS | 39 | -0.24 | -0.87 | 0.666 | 0.848 | 1.000 | 12145 | tags=26%, list=22%, signal=33% | |
3541 | REGULATION OF PROSTAGLANDIN SECRETION | 10 | -0.40 | -0.87 | 0.683 | 0.847 | 1.000 | 26493 | tags=70%, list=48%, signal=136% | |
3542 | SCF-DEPENDENT PROTEASOMAL UBIQUITIN-DEPENDENT PROTEIN CATABOLIC PROCESS | 40 | -0.27 | -0.87 | 0.697 | 0.847 | 1.000 | 29163 | tags=70%, list=53%, signal=150% | |
3543 | CRD-MEDIATED MRNA STABILIZATION | 22 | -0.28 | -0.87 | 0.620 | 0.847 | 1.000 | 24270 | tags=55%, list=44%, signal=98% | |
3544 | SECRETION | 741 | -0.21 | -0.87 | 0.675 | 0.847 | 1.000 | 23288 | tags=43%, list=43%, signal=74% | |
3545 | NEGATIVE REGULATION OF SMOOTH MUSCLE CELL DIFFERENTIATION | 7 | -0.36 | -0.87 | 0.652 | 0.847 | 1.000 | 33192 | tags=86%, list=61%, signal=218% | |
3546 | POSITIVE REGULATION OF ADENYLATE CYCLASE ACTIVITY | 77 | -0.23 | -0.87 | 0.683 | 0.848 | 1.000 | 26532 | tags=45%, list=49%, signal=88% | |
3547 | CELLULAR RESPONSE TO INTERFERON-ALPHA | 18 | -0.30 | -0.87 | 0.666 | 0.847 | 1.000 | 31967 | tags=72%, list=58%, signal=174% | |
3548 | DETECTION OF STIMULUS | 485 | -0.20 | -0.87 | 0.718 | 0.848 | 1.000 | 22998 | tags=40%, list=42%, signal=69% | |
3549 | REGULATION OF TRANSCRIPTION REGULATORY REGION DNA BINDING | 56 | -0.24 | -0.87 | 0.711 | 0.848 | 1.000 | 27343 | tags=50%, list=50%, signal=100% | |
3550 | POSITIVE REGULATION OF ARP2/3 COMPLEX-MEDIATED ACTIN NUCLEATION | 12 | -0.35 | -0.87 | 0.617 | 0.850 | 1.000 | 22819 | tags=67%, list=42%, signal=114% | |
3551 | CELLULAR RESPONSE TO ARSENIC-CONTAINING SUBSTANCE | 21 | -0.32 | -0.87 | 0.667 | 0.850 | 1.000 | 28396 | tags=67%, list=52%, signal=139% | |
3552 | VASCULAR ENDOTHELIAL GROWTH FACTOR SIGNALING PATHWAY | 35 | -0.26 | -0.87 | 0.656 | 0.850 | 1.000 | 30857 | tags=60%, list=56%, signal=138% | |
3553 | FATTY ACID ALPHA-OXIDATION | 12 | -0.35 | -0.87 | 0.626 | 0.850 | 1.000 | 35504 | tags=100%, list=65%, signal=285% | |
3554 | NEGATIVE REGULATION OF ANTIGEN RECEPTOR-MEDIATED SIGNALING PATHWAY | 40 | -0.27 | -0.87 | 0.676 | 0.850 | 1.000 | 12958 | tags=30%, list=24%, signal=39% | |
3555 | NEGATIVE REGULATION OF RECEPTOR BIOSYNTHETIC PROCESS | 22 | -0.29 | -0.87 | 0.659 | 0.850 | 1.000 | 35599 | tags=82%, list=65%, signal=234% | |
3556 | POSITIVE REGULATION OF HEMOPOIESIS | 226 | -0.22 | -0.87 | 0.697 | 0.850 | 1.000 | 27514 | tags=48%, list=50%, signal=96% | |
3557 | SALIVARY GLAND MORPHOGENESIS | 23 | -0.30 | -0.87 | 0.587 | 0.851 | 1.000 | 21813 | tags=43%, list=40%, signal=72% | |
3558 | POSITIVE REGULATION OF HEART CONTRACTION | 45 | -0.26 | -0.87 | 0.655 | 0.851 | 1.000 | 18367 | tags=31%, list=34%, signal=47% | |
3559 | REGULATION OF PHOSPHATIDYLINOSITOL 3-KINASE ACTIVITY | 62 | -0.22 | -0.87 | 0.675 | 0.850 | 1.000 | 22664 | tags=40%, list=41%, signal=69% | |
3560 | REGULATION OF GLUCOCORTICOID METABOLIC PROCESS | 17 | -0.31 | -0.87 | 0.636 | 0.850 | 1.000 | 7817 | tags=24%, list=14%, signal=27% | |
3561 | GLYCINE TRANSPORT | 7 | -0.39 | -0.87 | 0.628 | 0.850 | 1.000 | 29166 | tags=71%, list=53%, signal=153% | |
3562 | REGULATION OF T-HELPER 2 CELL DIFFERENTIATION | 16 | -0.31 | -0.87 | 0.629 | 0.850 | 1.000 | 4564 | tags=19%, list=8%, signal=20% | |
3563 | REGULATION OF MYELOID LEUKOCYTE DIFFERENTIATION | 134 | -0.23 | -0.87 | 0.664 | 0.850 | 1.000 | 27116 | tags=48%, list=50%, signal=95% | |
3564 | CYTOPLASMIC TRANSLATION | 16 | -0.33 | -0.87 | 0.616 | 0.851 | 1.000 | 35170 | tags=94%, list=64%, signal=263% | |
3565 | CYTOPLASMIC TRANSLATIONAL INITIATION | 16 | -0.33 | -0.87 | 0.616 | 0.850 | 1.000 | 35170 | tags=94%, list=64%, signal=263% | |
3566 | MIRNA MEDIATED INHIBITION OF TRANSLATION | 26 | -0.31 | -0.87 | 0.616 | 0.850 | 1.000 | 31630 | tags=73%, list=58%, signal=173% | |
3567 | NEGATIVE REGULATION OF TRANSLATION, NCRNA-MEDIATED | 26 | -0.31 | -0.87 | 0.616 | 0.850 | 1.000 | 31630 | tags=73%, list=58%, signal=173% | |
3568 | REGULATION OF TRANSLATION, NCRNA-MEDIATED | 26 | -0.31 | -0.87 | 0.616 | 0.850 | 1.000 | 31630 | tags=73%, list=58%, signal=173% | |
3569 | ANGIOTENSIN MATURATION | 21 | -0.30 | -0.87 | 0.644 | 0.850 | 1.000 | 13274 | tags=29%, list=24%, signal=38% | |
3570 | EMBRYONIC CRANIAL SKELETON MORPHOGENESIS | 41 | -0.26 | -0.86 | 0.633 | 0.850 | 1.000 | 16824 | tags=34%, list=31%, signal=49% | |
3571 | HISTONE H3-K4 DEMETHYLATION | 10 | -0.37 | -0.86 | 0.657 | 0.850 | 1.000 | 21453 | tags=60%, list=39%, signal=99% | |
3572 | POSITIVE REGULATION OF GROWTH | 340 | -0.20 | -0.86 | 0.749 | 0.850 | 1.000 | 30336 | tags=55%, list=55%, signal=123% | |
3573 | POSITIVE REGULATION OF CELL-MATRIX ADHESION | 80 | -0.23 | -0.86 | 0.678 | 0.850 | 1.000 | 30781 | tags=61%, list=56%, signal=140% | |
3574 | MEMBRANE LIPID CATABOLIC PROCESS | 27 | -0.28 | -0.86 | 0.640 | 0.850 | 1.000 | 28614 | tags=63%, list=52%, signal=132% | |
3575 | REGULATION OF AXON EXTENSION | 90 | -0.22 | -0.86 | 0.696 | 0.850 | 1.000 | 28543 | tags=54%, list=52%, signal=114% | |
3576 | WNT SIGNALING PATHWAY | 184 | -0.23 | -0.86 | 0.742 | 0.850 | 1.000 | 20339 | tags=42%, list=37%, signal=66% | |
3577 | REGULATION OF SECONDARY METABOLIC PROCESS | 8 | -0.35 | -0.86 | 0.690 | 0.850 | 1.000 | 35476 | tags=100%, list=65%, signal=285% | |
3578 | REGULATION OF FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 41 | -0.25 | -0.86 | 0.649 | 0.850 | 1.000 | 13537 | tags=32%, list=25%, signal=42% | |
3579 | PURINE NUCLEOSIDE CATABOLIC PROCESS | 15 | -0.30 | -0.86 | 0.653 | 0.850 | 1.000 | 13347 | tags=33%, list=24%, signal=44% | |
3580 | PURINE RIBONUCLEOSIDE CATABOLIC PROCESS | 15 | -0.30 | -0.86 | 0.653 | 0.850 | 1.000 | 13347 | tags=33%, list=24%, signal=44% | |
3581 | PROTEIN K48-LINKED DEUBIQUITINATION | 57 | -0.26 | -0.86 | 0.606 | 0.850 | 1.000 | 23060 | tags=49%, list=42%, signal=85% | |
3582 | REGULATION OF MESONEPHROS DEVELOPMENT | 42 | -0.25 | -0.86 | 0.649 | 0.850 | 1.000 | 17093 | tags=33%, list=31%, signal=48% | |
3583 | GLYCOSAMINOGLYCAN BIOSYNTHETIC PROCESS | 222 | -0.21 | -0.86 | 0.661 | 0.851 | 1.000 | 21375 | tags=41%, list=39%, signal=66% | |
3584 | POSITIVE REGULATION OF LEUKOCYTE DIFFERENTIATION | 162 | -0.22 | -0.86 | 0.706 | 0.851 | 1.000 | 27378 | tags=46%, list=50%, signal=92% | |
3585 | REGULATION OF ADHERENS JUNCTION ORGANIZATION | 132 | -0.22 | -0.86 | 0.688 | 0.852 | 1.000 | 30488 | tags=60%, list=56%, signal=135% | |
3586 | OXIDATIVE DEMETHYLATION | 40 | -0.25 | -0.86 | 0.657 | 0.852 | 1.000 | 32064 | tags=68%, list=59%, signal=163% | |
3587 | REGULATION OF NUCLEOTIDE CATABOLIC PROCESS | 67 | -0.25 | -0.86 | 0.698 | 0.852 | 1.000 | 25775 | tags=54%, list=47%, signal=102% | |
3588 | BIOMINERAL TISSUE DEVELOPMENT | 58 | -0.24 | -0.86 | 0.658 | 0.852 | 1.000 | 30219 | tags=57%, list=55%, signal=127% | |
3589 | ACTIVATION OF JNKK ACTIVITY | 9 | -0.30 | -0.86 | 0.630 | 0.851 | 1.000 | 8319 | tags=33%, list=15%, signal=39% | |
3590 | POSITIVE REGULATION OF CYTOKINE SECRETION | 131 | -0.23 | -0.86 | 0.684 | 0.852 | 1.000 | 13890 | tags=31%, list=25%, signal=41% | |
3591 | AMINOGLYCAN BIOSYNTHETIC PROCESS | 223 | -0.21 | -0.86 | 0.668 | 0.852 | 1.000 | 21375 | tags=40%, list=39%, signal=66% | |
3592 | TUBE DEVELOPMENT | 457 | -0.19 | -0.86 | 0.727 | 0.853 | 1.000 | 31201 | tags=55%, list=57%, signal=127% | |
3593 | REGULATION OF INTERLEUKIN-1 PRODUCTION | 74 | -0.26 | -0.86 | 0.686 | 0.852 | 1.000 | 16702 | tags=35%, list=31%, signal=51% | |
3594 | PROTEIN MANNOSYLATION | 13 | -0.32 | -0.86 | 0.648 | 0.853 | 1.000 | 28125 | tags=69%, list=51%, signal=143% | |
3595 | PROTEIN O-LINKED MANNOSYLATION | 13 | -0.32 | -0.86 | 0.648 | 0.853 | 1.000 | 28125 | tags=69%, list=51%, signal=143% | |
3596 | RESPONSE TO MURAMYL DIPEPTIDE | 24 | -0.30 | -0.86 | 0.635 | 0.853 | 1.000 | 26936 | tags=63%, list=49%, signal=123% | |
3597 | CELL-CELL JUNCTION ASSEMBLY | 156 | -0.23 | -0.86 | 0.752 | 0.853 | 1.000 | 25849 | tags=51%, list=47%, signal=96% | |
3598 | NEURON PROJECTION EXTENSION | 52 | -0.24 | -0.86 | 0.644 | 0.853 | 1.000 | 16029 | tags=35%, list=29%, signal=49% | |
3599 | ACTIVATION OF NF-KAPPAB-INDUCING KINASE ACTIVITY | 28 | -0.26 | -0.86 | 0.656 | 0.854 | 1.000 | 23080 | tags=54%, list=42%, signal=93% | |
3600 | DORSAL/VENTRAL PATTERN FORMATION | 61 | -0.23 | -0.86 | 0.656 | 0.854 | 1.000 | 18808 | tags=36%, list=34%, signal=55% | |
3601 | POSITIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 502 | -0.20 | -0.86 | 0.747 | 0.854 | 1.000 | 28569 | tags=52%, list=52%, signal=108% | |
3602 | ACTIN FILAMENT-BASED MOVEMENT | 164 | -0.20 | -0.86 | 0.714 | 0.854 | 1.000 | 20955 | tags=37%, list=38%, signal=59% | |
3603 | REGULATION OF NEUROLOGICAL SYSTEM PROCESS | 41 | -0.26 | -0.86 | 0.695 | 0.854 | 1.000 | 22607 | tags=46%, list=41%, signal=79% | |
3604 | LYMPHATIC ENDOTHELIAL CELL DIFFERENTIATION | 20 | -0.30 | -0.86 | 0.656 | 0.854 | 1.000 | 18077 | tags=45%, list=33%, signal=67% | |
3605 | ACTIN FILAMENT CAPPING | 24 | -0.27 | -0.86 | 0.664 | 0.853 | 1.000 | 19184 | tags=42%, list=35%, signal=64% | |
3606 | HISTONE H4-K20 DEMETHYLATION | 16 | -0.31 | -0.86 | 0.656 | 0.853 | 1.000 | 30141 | tags=69%, list=55%, signal=153% | |
3607 | DNA REPLICATION-INDEPENDENT NUCLEOSOME ASSEMBLY | 97 | -0.25 | -0.86 | 0.711 | 0.854 | 1.000 | 34810 | tags=77%, list=64%, signal=212% | |
3608 | DNA REPLICATION-INDEPENDENT NUCLEOSOME ORGANIZATION | 97 | -0.25 | -0.86 | 0.711 | 0.854 | 1.000 | 34810 | tags=77%, list=64%, signal=212% | |
3609 | POSITIVE REGULATION OF MITOTIC CELL CYCLE | 227 | -0.22 | -0.86 | 0.746 | 0.854 | 1.000 | 28774 | tags=56%, list=53%, signal=117% | |
3610 | RESPONSE TO CAMP | 80 | -0.23 | -0.86 | 0.717 | 0.854 | 1.000 | 16270 | tags=33%, list=30%, signal=46% | |
3611 | POSITIVE REGULATION OF RESPIRATORY BURST | 41 | -0.26 | -0.86 | 0.636 | 0.854 | 1.000 | 12145 | tags=22%, list=22%, signal=28% | |
3612 | VASCULAR SMOOTH MUSCLE CELL DIFFERENTIATION | 17 | -0.30 | -0.86 | 0.612 | 0.854 | 1.000 | 27706 | tags=59%, list=51%, signal=119% | |
3613 | MODULATION OF SYNAPTIC TRANSMISSION | 271 | -0.19 | -0.86 | 0.692 | 0.854 | 1.000 | 18483 | tags=33%, list=34%, signal=49% | |
3614 | REGULATION OF SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 104 | -0.23 | -0.86 | 0.712 | 0.854 | 1.000 | 29099 | tags=59%, list=53%, signal=125% | |
3615 | POSITIVE REGULATION OF NEUROGENESIS | 457 | -0.20 | -0.86 | 0.771 | 0.855 | 1.000 | 28569 | tags=53%, list=52%, signal=110% | |
3616 | REGULATION OF HEXOKINASE ACTIVITY | 10 | -0.35 | -0.86 | 0.626 | 0.854 | 1.000 | 28674 | tags=70%, list=52%, signal=147% | |
3617 | POSITIVE REGULATION OF RESPONSE TO TUMOR CELL | 22 | -0.27 | -0.86 | 0.640 | 0.854 | 1.000 | 17597 | tags=41%, list=32%, signal=60% | |
3618 | POSITIVE REGULATION OF IMMUNE RESPONSE TO TUMOR CELL | 22 | -0.27 | -0.86 | 0.640 | 0.854 | 1.000 | 17597 | tags=41%, list=32%, signal=60% | |
3619 | REGULATION OF DEVELOPMENTAL GROWTH | 320 | -0.19 | -0.86 | 0.735 | 0.854 | 1.000 | 28543 | tags=49%, list=52%, signal=102% | |
3620 | EPITHELIAL TUBE BRANCHING INVOLVED IN LUNG MORPHOGENESIS | 16 | -0.32 | -0.86 | 0.631 | 0.854 | 1.000 | 21813 | tags=50%, list=40%, signal=83% | |
3621 | RECEPTOR-MEDIATED ENDOCYTOSIS | 426 | -0.21 | -0.86 | 0.653 | 0.854 | 1.000 | 23264 | tags=41%, list=43%, signal=71% | |
3622 | REGULATION OF T CELL RECEPTOR SIGNALING PATHWAY | 48 | -0.26 | -0.86 | 0.681 | 0.854 | 1.000 | 11326 | tags=27%, list=21%, signal=34% | |
3623 | THYMUS DEVELOPMENT | 27 | -0.25 | -0.86 | 0.662 | 0.854 | 1.000 | 34790 | tags=70%, list=64%, signal=193% | |
3624 | REGULATION OF EPIDERMAL CELL DIFFERENTIATION | 56 | -0.24 | -0.86 | 0.688 | 0.854 | 1.000 | 29343 | tags=64%, list=54%, signal=139% | |
3625 | NEGATIVE REGULATION OF STRIATED MUSCLE CELL APOPTOTIC PROCESS | 15 | -0.31 | -0.86 | 0.628 | 0.855 | 1.000 | 19469 | tags=40%, list=36%, signal=62% | |
3626 | CELL PROJECTION ASSEMBLY | 457 | -0.23 | -0.86 | 0.646 | 0.855 | 1.000 | 34624 | tags=71%, list=63%, signal=192% | |
3627 | RENAL SYSTEM PROCESS INVOLVED IN REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE | 30 | -0.26 | -0.86 | 0.643 | 0.855 | 1.000 | 28804 | tags=67%, list=53%, signal=141% | |
3628 | BASIC AMINO ACID TRANSPORT | 19 | -0.28 | -0.86 | 0.652 | 0.856 | 1.000 | 9409 | tags=26%, list=17%, signal=32% | |
3629 | POSITIVE REGULATION OF ALPHA-BETA T CELL DIFFERENTIATION | 43 | -0.25 | -0.86 | 0.646 | 0.856 | 1.000 | 16824 | tags=33%, list=31%, signal=47% | |
3630 | CELLULAR RESPONSE TO ATP | 20 | -0.26 | -0.86 | 0.649 | 0.855 | 1.000 | 15673 | tags=35%, list=29%, signal=49% | |
3631 | BLOOD COAGULATION, EXTRINSIC PATHWAY | 10 | -0.36 | -0.86 | 0.634 | 0.856 | 1.000 | 21039 | tags=60%, list=38%, signal=98% | |
3632 | DETECTION OF EXTERNAL STIMULUS | 262 | -0.20 | -0.86 | 0.744 | 0.856 | 1.000 | 19295 | tags=35%, list=35%, signal=54% | |
3633 | REGULATION OF MICROTUBULE-BASED MOVEMENT | 32 | -0.27 | -0.86 | 0.618 | 0.856 | 1.000 | 33316 | tags=75%, list=61%, signal=192% | |
3634 | FOREBRAIN CELL MIGRATION | 50 | -0.25 | -0.86 | 0.636 | 0.856 | 1.000 | 36712 | tags=78%, list=67%, signal=237% | |
3635 | PEPTIDYL-THREONINE MODIFICATION | 132 | -0.23 | -0.86 | 0.666 | 0.856 | 1.000 | 18140 | tags=39%, list=33%, signal=58% | |
3636 | NEGATIVE REGULATION OF LEUKOCYTE MEDIATED IMMUNITY | 78 | -0.27 | -0.85 | 0.653 | 0.856 | 1.000 | 9310 | tags=24%, list=17%, signal=29% | |
3637 | POSITIVE REGULATION OF T-HELPER 17 TYPE IMMUNE RESPONSE | 10 | -0.38 | -0.85 | 0.650 | 0.856 | 1.000 | 27378 | tags=70%, list=50%, signal=140% | |
3638 | PEPTIDYL-THREONINE DEPHOSPHORYLATION | 22 | -0.31 | -0.85 | 0.650 | 0.857 | 1.000 | 28259 | tags=73%, list=52%, signal=150% | |
3639 | RESPONSE TO BMP | 143 | -0.22 | -0.85 | 0.764 | 0.857 | 1.000 | 15477 | tags=31%, list=28%, signal=44% | |
3640 | CELLULAR RESPONSE TO BMP STIMULUS | 143 | -0.22 | -0.85 | 0.764 | 0.857 | 1.000 | 15477 | tags=31%, list=28%, signal=44% | |
3641 | EMBRYONIC SKELETAL JOINT MORPHOGENESIS | 8 | -0.34 | -0.85 | 0.663 | 0.857 | 1.000 | 30361 | tags=63%, list=56%, signal=141% | |
3642 | CLATHRIN COAT ASSEMBLY | 25 | -0.30 | -0.85 | 0.677 | 0.858 | 1.000 | 26003 | tags=60%, list=48%, signal=114% | |
3643 | REGULATION OF BMP SIGNALING PATHWAY | 105 | -0.21 | -0.85 | 0.740 | 0.858 | 1.000 | 11990 | tags=24%, list=22%, signal=30% | |
3644 | NEURAL RETINA DEVELOPMENT | 64 | -0.22 | -0.85 | 0.704 | 0.859 | 1.000 | 7016 | tags=19%, list=13%, signal=21% | |
3645 | REGULATION OF RESPONSE TO INTERFERON-GAMMA | 57 | -0.25 | -0.85 | 0.651 | 0.860 | 1.000 | 23799 | tags=51%, list=44%, signal=90% | |
3646 | ORGAN OR TISSUE SPECIFIC IMMUNE RESPONSE | 38 | -0.26 | -0.85 | 0.684 | 0.860 | 1.000 | 7301 | tags=24%, list=13%, signal=27% | |
3647 | POSITIVE REGULATION OF PHAGOCYTOSIS | 61 | -0.25 | -0.85 | 0.645 | 0.860 | 1.000 | 16737 | tags=36%, list=31%, signal=52% | |
3648 | PATTERN SPECIFICATION PROCESS | 335 | -0.20 | -0.85 | 0.767 | 0.860 | 1.000 | 30257 | tags=55%, list=55%, signal=122% | |
3649 | MOLTING CYCLE | 67 | -0.23 | -0.85 | 0.656 | 0.860 | 1.000 | 34080 | tags=66%, list=62%, signal=174% | |
3650 | HAIR CYCLE | 67 | -0.23 | -0.85 | 0.656 | 0.860 | 1.000 | 34080 | tags=66%, list=62%, signal=174% | |
3651 | MAGNESIUM ION TRANSMEMBRANE TRANSPORT | 14 | -0.33 | -0.85 | 0.635 | 0.860 | 1.000 | 35035 | tags=93%, list=64%, signal=258% | |
3652 | MITOCHONDRIAL GENOME MAINTENANCE | 32 | -0.29 | -0.85 | 0.685 | 0.860 | 1.000 | 29047 | tags=72%, list=53%, signal=153% | |
3653 | GLYCOSPHINGOLIPID METABOLIC PROCESS | 111 | -0.23 | -0.85 | 0.691 | 0.859 | 1.000 | 35113 | tags=73%, list=64%, signal=204% | |
3654 | UNSATURATED FATTY ACID BIOSYNTHETIC PROCESS | 84 | -0.24 | -0.85 | 0.678 | 0.860 | 1.000 | 28795 | tags=58%, list=53%, signal=123% | |
3655 | PEPTIDYL-ARGININE METHYLATION, TO ASYMMETRICAL-DIMETHYL ARGININE | 6 | -0.38 | -0.85 | 0.658 | 0.860 | 1.000 | 33653 | tags=100%, list=62%, signal=260% | |
3656 | REGULATION OF PHAGOCYTOSIS | 80 | -0.25 | -0.85 | 0.667 | 0.860 | 1.000 | 17837 | tags=39%, list=33%, signal=57% | |
3657 | ICOSANOID BIOSYNTHETIC PROCESS | 68 | -0.25 | -0.85 | 0.654 | 0.860 | 1.000 | 28795 | tags=60%, list=53%, signal=127% | |
3658 | FATTY ACID DERIVATIVE BIOSYNTHETIC PROCESS | 68 | -0.25 | -0.85 | 0.654 | 0.859 | 1.000 | 28795 | tags=60%, list=53%, signal=127% | |
3659 | REGULATION OF FIBROBLAST APOPTOTIC PROCESS | 32 | -0.27 | -0.85 | 0.672 | 0.859 | 1.000 | 13770 | tags=38%, list=25%, signal=50% | |
3660 | POSITIVE REGULATION OF ENDOTHELIAL CELL DIFFERENTIATION | 12 | -0.35 | -0.85 | 0.637 | 0.859 | 1.000 | 11366 | tags=33%, list=21%, signal=42% | |
3661 | REGULATION OF MONOCYTE CHEMOTACTIC PROTEIN-1 PRODUCTION | 12 | -0.34 | -0.85 | 0.690 | 0.859 | 1.000 | 19886 | tags=50%, list=36%, signal=79% | |
3662 | GLYCEROL METABOLIC PROCESS | 15 | -0.30 | -0.85 | 0.618 | 0.859 | 1.000 | 10537 | tags=27%, list=19%, signal=33% | |
3663 | KERATAN SULFATE BIOSYNTHETIC PROCESS | 72 | -0.24 | -0.85 | 0.708 | 0.859 | 1.000 | 31656 | tags=60%, list=58%, signal=142% | |
3664 | RESPONSE TO XENOBIOTIC STIMULUS | 365 | -0.20 | -0.85 | 0.714 | 0.860 | 1.000 | 27021 | tags=50%, list=49%, signal=99% | |
3665 | SEXUAL REPRODUCTION | 462 | -0.19 | -0.85 | 0.814 | 0.860 | 1.000 | 21886 | tags=39%, list=40%, signal=64% | |
3666 | RIBOSOME DISASSEMBLY | 16 | -0.33 | -0.85 | 0.619 | 0.860 | 1.000 | 19655 | tags=56%, list=36%, signal=88% | |
3667 | POSITIVE REGULATION OF LIPID CATABOLIC PROCESS | 60 | -0.23 | -0.85 | 0.719 | 0.860 | 1.000 | 23466 | tags=45%, list=43%, signal=79% | |
3668 | BUNDLE OF HIS CELL TO PURKINJE MYOCYTE SIGNALING | 3 | -0.52 | -0.85 | 0.696 | 0.860 | 1.000 | 24367 | tags=67%, list=45%, signal=120% | |
3669 | BUNDLE OF HIS CELL ACTION POTENTIAL | 3 | -0.52 | -0.85 | 0.696 | 0.860 | 1.000 | 24367 | tags=67%, list=45%, signal=120% | |
3670 | DETECTION OF ABIOTIC STIMULUS | 270 | -0.19 | -0.85 | 0.750 | 0.860 | 1.000 | 19295 | tags=35%, list=35%, signal=54% | |
3671 | POSITIVE REGULATION OF CELLULAR COMPONENT MOVEMENT | 723 | -0.20 | -0.85 | 0.779 | 0.860 | 1.000 | 30306 | tags=54%, list=55%, signal=120% | |
3672 | INTESTINAL ABSORPTION | 34 | -0.25 | -0.85 | 0.710 | 0.860 | 1.000 | 30626 | tags=62%, list=56%, signal=140% | |
3673 | POSITIVE REGULATION OF GLUCOSE IMPORT | 68 | -0.23 | -0.85 | 0.707 | 0.861 | 1.000 | 30907 | tags=62%, list=57%, signal=142% | |
3674 | STEROID HORMONE MEDIATED SIGNALING PATHWAY | 51 | -0.23 | -0.85 | 0.707 | 0.861 | 1.000 | 29187 | tags=55%, list=53%, signal=118% | |
3675 | REGULATION OF DOUBLE-STRAND BREAK REPAIR VIA HOMOLOGOUS RECOMBINATION | 29 | -0.27 | -0.85 | 0.703 | 0.860 | 1.000 | 33477 | tags=72%, list=61%, signal=187% | |
3676 | MOTILE CILIUM ASSEMBLY | 23 | -0.32 | -0.85 | 0.592 | 0.861 | 1.000 | 35670 | tags=91%, list=65%, signal=263% | |
3677 | NEGATIVE REGULATION OF TELOMERE CAPPING | 19 | -0.31 | -0.85 | 0.649 | 0.860 | 1.000 | 12657 | tags=32%, list=23%, signal=41% | |
3678 | REGULATION OF LIPID STORAGE | 96 | -0.24 | -0.85 | 0.697 | 0.861 | 1.000 | 38021 | tags=81%, list=70%, signal=266% | |
3679 | MONOCYTE ACTIVATION | 17 | -0.32 | -0.85 | 0.666 | 0.861 | 1.000 | 37147 | tags=100%, list=68%, signal=312% | |
3680 | METANEPHRIC MESENCHYME DEVELOPMENT | 19 | -0.27 | -0.85 | 0.661 | 0.861 | 1.000 | 16194 | tags=37%, list=30%, signal=52% | |
3681 | GLAND DEVELOPMENT | 228 | -0.20 | -0.85 | 0.748 | 0.861 | 1.000 | 21892 | tags=39%, list=40%, signal=66% | |
3682 | DIGESTIVE SYSTEM PROCESS | 65 | -0.24 | -0.85 | 0.704 | 0.861 | 1.000 | 21434 | tags=45%, list=39%, signal=73% | |
3683 | REGULATION OF GLUCOCORTICOID RECEPTOR SIGNALING PATHWAY | 18 | -0.29 | -0.85 | 0.643 | 0.861 | 1.000 | 27941 | tags=67%, list=51%, signal=136% | |
3684 | XENOBIOTIC METABOLIC PROCESS | 363 | -0.20 | -0.85 | 0.720 | 0.861 | 1.000 | 27021 | tags=50%, list=49%, signal=99% | |
3685 | AXIS SPECIFICATION | 93 | -0.23 | -0.85 | 0.699 | 0.863 | 1.000 | 20399 | tags=39%, list=37%, signal=62% | |
3686 | REGULATION OF CARBOHYDRATE CATABOLIC PROCESS | 67 | -0.24 | -0.85 | 0.733 | 0.864 | 1.000 | 28192 | tags=58%, list=52%, signal=120% | |
3687 | REGULATION OF CELLULAR CARBOHYDRATE CATABOLIC PROCESS | 67 | -0.24 | -0.85 | 0.733 | 0.863 | 1.000 | 28192 | tags=58%, list=52%, signal=120% | |
3688 | ENDOCARDIUM MORPHOGENESIS | 11 | -0.33 | -0.85 | 0.671 | 0.863 | 1.000 | 22985 | tags=55%, list=42%, signal=94% | |
3689 | POSITIVE REGULATION OF LOCOMOTION | 731 | -0.20 | -0.85 | 0.786 | 0.863 | 1.000 | 31064 | tags=56%, list=57%, signal=128% | |
3690 | GLYCOSIDE METABOLIC PROCESS | 27 | -0.31 | -0.85 | 0.640 | 0.863 | 1.000 | 33676 | tags=85%, list=62%, signal=222% | |
3691 | CELLULAR RESPONSE TO DRUG | 67 | -0.23 | -0.85 | 0.692 | 0.863 | 1.000 | 29286 | tags=57%, list=54%, signal=122% | |
3692 | POSITIVE REGULATION OF NOTCH SIGNALING PATHWAY | 44 | -0.23 | -0.84 | 0.692 | 0.864 | 1.000 | 12962 | tags=30%, list=24%, signal=39% | |
3693 | ECTODERM DEVELOPMENT | 25 | -0.27 | -0.84 | 0.692 | 0.864 | 1.000 | 22673 | tags=44%, list=41%, signal=75% | |
3694 | REGULATION OF T-HELPER 1 CELL DIFFERENTIATION | 12 | -0.32 | -0.84 | 0.646 | 0.864 | 1.000 | 30991 | tags=58%, list=57%, signal=135% | |
3695 | RECEPTOR TRANSACTIVATION | 13 | -0.34 | -0.84 | 0.623 | 0.864 | 1.000 | 7306 | tags=23%, list=13%, signal=27% | |
3696 | POSITIVE REGULATION OF PHOSPHATASE ACTIVITY | 49 | -0.25 | -0.84 | 0.686 | 0.864 | 1.000 | 31989 | tags=65%, list=59%, signal=157% | |
3697 | ODONTOGENESIS OF DENTIN-CONTAINING TOOTH | 52 | -0.24 | -0.84 | 0.674 | 0.864 | 1.000 | 21962 | tags=40%, list=40%, signal=67% | |
3698 | REGULATION OF EPIDERMIS DEVELOPMENT | 70 | -0.23 | -0.84 | 0.707 | 0.864 | 1.000 | 29343 | tags=61%, list=54%, signal=132% | |
3699 | POSITIVE REGULATION OF PROTEIN EXPORT FROM NUCLEUS | 28 | -0.28 | -0.84 | 0.703 | 0.864 | 1.000 | 28032 | tags=64%, list=51%, signal=132% | |
3700 | REGULATION OF HISTONE H3-K9 ACETYLATION | 30 | -0.27 | -0.84 | 0.723 | 0.864 | 1.000 | 34524 | tags=77%, list=63%, signal=208% | |
3701 | TYROSINE PHOSPHORYLATION OF STAT PROTEIN | 17 | -0.30 | -0.84 | 0.656 | 0.863 | 1.000 | 35855 | tags=82%, list=66%, signal=239% | |
3702 | REGULATION OF ESTABLISHMENT OF PLANAR POLARITY | 34 | -0.24 | -0.84 | 0.690 | 0.863 | 1.000 | 31954 | tags=65%, list=58%, signal=156% | |
3703 | EAR DEVELOPMENT | 109 | -0.22 | -0.84 | 0.715 | 0.863 | 1.000 | 30361 | tags=54%, list=56%, signal=121% | |
3704 | REGULATION OF HEMATOPOIETIC PROGENITOR CELL DIFFERENTIATION | 75 | -0.22 | -0.84 | 0.749 | 0.864 | 1.000 | 34452 | tags=71%, list=63%, signal=191% | |
3705 | NEGATIVE REGULATION OF KIDNEY DEVELOPMENT | 34 | -0.27 | -0.84 | 0.669 | 0.864 | 1.000 | 19886 | tags=41%, list=36%, signal=65% | |
3706 | SPERM MOTILITY | 53 | -0.26 | -0.84 | 0.655 | 0.864 | 1.000 | 21159 | tags=47%, list=39%, signal=77% | |
3707 | REGULATION OF LEUKOCYTE CHEMOTAXIS | 135 | -0.23 | -0.84 | 0.687 | 0.864 | 1.000 | 16947 | tags=34%, list=31%, signal=49% | |
3708 | SINGLE ORGANISM REPRODUCTIVE PROCESS | 773 | -0.19 | -0.84 | 0.833 | 0.864 | 1.000 | 21925 | tags=38%, list=40%, signal=62% | |
3709 | POSITIVE REGULATION OF INTERLEUKIN-12 PRODUCTION | 50 | -0.26 | -0.84 | 0.674 | 0.864 | 1.000 | 17769 | tags=40%, list=32%, signal=59% | |
3710 | LEPTIN-MEDIATED SIGNALING PATHWAY | 19 | -0.30 | -0.84 | 0.661 | 0.864 | 1.000 | 33223 | tags=84%, list=61%, signal=215% | |
3711 | CELLULAR RESPONSE TO XENOBIOTIC STIMULUS | 364 | -0.20 | -0.84 | 0.729 | 0.864 | 1.000 | 27021 | tags=50%, list=49%, signal=99% | |
3712 | NEGATIVE REGULATION OF HEMOPOIESIS | 180 | -0.21 | -0.84 | 0.735 | 0.865 | 1.000 | 27244 | tags=49%, list=50%, signal=98% | |
3713 | REGULATION OF NATURAL KILLER CELL MEDIATED IMMUNE RESPONSE TO TUMOR CELL | 15 | -0.28 | -0.84 | 0.656 | 0.865 | 1.000 | 20528 | tags=47%, list=38%, signal=75% | |
3714 | POSITIVE REGULATION OF NATURAL KILLER CELL MEDIATED IMMUNE RESPONSE TO TUMOR CELL | 15 | -0.28 | -0.84 | 0.656 | 0.865 | 1.000 | 20528 | tags=47%, list=38%, signal=75% | |
3715 | REGULATION OF NATURAL KILLER CELL MEDIATED CYTOTOXICITY DIRECTED AGAINST TUMOR CELL TARGET | 15 | -0.28 | -0.84 | 0.656 | 0.865 | 1.000 | 20528 | tags=47%, list=38%, signal=75% | |
3716 | POSITIVE REGULATION OF NATURAL KILLER CELL MEDIATED CYTOTOXICITY DIRECTED AGAINST TUMOR CELL TARGET | 15 | -0.28 | -0.84 | 0.656 | 0.864 | 1.000 | 20528 | tags=47%, list=38%, signal=75% | |
3717 | MESODERMAL CELL FATE COMMITMENT | 12 | -0.31 | -0.84 | 0.679 | 0.865 | 1.000 | 14059 | tags=33%, list=26%, signal=45% | |
3718 | RNA SECONDARY STRUCTURE UNWINDING | 22 | -0.31 | -0.84 | 0.609 | 0.865 | 1.000 | 4858 | tags=23%, list=9%, signal=25% | |
3719 | REGULATION OF GLUCOSE IMPORT | 96 | -0.21 | -0.84 | 0.751 | 0.865 | 1.000 | 30907 | tags=58%, list=57%, signal=134% | |
3720 | PROTEOGLYCAN METABOLIC PROCESS | 160 | -0.21 | -0.84 | 0.722 | 0.865 | 1.000 | 21261 | tags=41%, list=39%, signal=66% | |
3721 | NEGATIVE REGULATION OF OSTEOBLAST DIFFERENTIATION | 49 | -0.23 | -0.84 | 0.688 | 0.865 | 1.000 | 6207 | tags=18%, list=11%, signal=21% | |
3722 | POSITIVE REGULATION OF MONOOXYGENASE ACTIVITY | 50 | -0.26 | -0.84 | 0.669 | 0.865 | 1.000 | 11121 | tags=24%, list=20%, signal=30% | |
3723 | POSITIVE REGULATION OF RAS PROTEIN SIGNAL TRANSDUCTION | 56 | -0.24 | -0.84 | 0.672 | 0.865 | 1.000 | 18711 | tags=36%, list=34%, signal=54% | |
3724 | POSITIVE REGULATION OF ERYTHROCYTE DIFFERENTIATION | 42 | -0.25 | -0.84 | 0.688 | 0.865 | 1.000 | 38019 | tags=76%, list=70%, signal=250% | |
3725 | POSTSYNAPTIC DENSITY ORGANIZATION | 22 | -0.29 | -0.84 | 0.653 | 0.865 | 1.000 | 18246 | tags=41%, list=33%, signal=61% | |
3726 | POSTSYNAPTIC DENSITY ASSEMBLY | 22 | -0.29 | -0.84 | 0.653 | 0.865 | 1.000 | 18246 | tags=41%, list=33%, signal=61% | |
3727 | REGULATION OF NEUROTRANSMITTER SECRETION | 51 | -0.22 | -0.84 | 0.709 | 0.865 | 1.000 | 17863 | tags=33%, list=33%, signal=49% | |
3728 | REGULATION OF SPINDLE ASSEMBLY | 27 | -0.31 | -0.84 | 0.640 | 0.865 | 1.000 | 25722 | tags=63%, list=47%, signal=119% | |
3729 | OXIDATIVE DNA DEMETHYLATION | 12 | -0.33 | -0.84 | 0.678 | 0.866 | 1.000 | 16304 | tags=42%, list=30%, signal=59% | |
3730 | PHOSPHATIDYLINOSITOL-MEDIATED SIGNALING | 372 | -0.20 | -0.84 | 0.813 | 0.867 | 1.000 | 31686 | tags=59%, list=58%, signal=139% | |
3731 | INOSITOL LIPID-MEDIATED SIGNALING | 372 | -0.20 | -0.84 | 0.813 | 0.867 | 1.000 | 31686 | tags=59%, list=58%, signal=139% | |
3732 | PROLINE TRANSPORT | 16 | -0.27 | -0.84 | 0.657 | 0.867 | 1.000 | 22668 | tags=56%, list=41%, signal=96% | |
3733 | POSITIVE REGULATION OF DENDRITIC SPINE MORPHOGENESIS | 22 | -0.27 | -0.84 | 0.666 | 0.867 | 1.000 | 28697 | tags=64%, list=52%, signal=134% | |
3734 | REGULATION OF PRO-B CELL DIFFERENTIATION | 16 | -0.30 | -0.84 | 0.667 | 0.867 | 1.000 | 29422 | tags=63%, list=54%, signal=135% | |
3735 | PLATELET-DERIVED GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 51 | -0.23 | -0.84 | 0.711 | 0.867 | 1.000 | 24797 | tags=47%, list=45%, signal=86% | |
3736 | RESPONSE TO VITAMIN D | 21 | -0.29 | -0.84 | 0.698 | 0.867 | 1.000 | 28737 | tags=71%, list=53%, signal=151% | |
3737 | RESPONSE TO LIPOPOLYSACCHARIDE | 227 | -0.24 | -0.84 | 0.709 | 0.867 | 1.000 | 20612 | tags=41%, list=38%, signal=65% | |
3738 | RESPONSE TO INTERLEUKIN-1 | 124 | -0.22 | -0.84 | 0.737 | 0.867 | 1.000 | 14239 | tags=28%, list=26%, signal=38% | |
3739 | NEGATIVE REGULATION OF CELL ADHESION | 388 | -0.21 | -0.84 | 0.762 | 0.867 | 1.000 | 31655 | tags=59%, list=58%, signal=139% | |
3740 | FERROUS IRON TRANSPORT | 14 | -0.30 | -0.84 | 0.646 | 0.867 | 1.000 | 9138 | tags=29%, list=17%, signal=34% | |
3741 | REGULATION OF HYDROGEN PEROXIDE METABOLIC PROCESS | 18 | -0.33 | -0.84 | 0.660 | 0.867 | 1.000 | 15479 | tags=44%, list=28%, signal=62% | |
3742 | CARDIAC CHAMBER DEVELOPMENT | 167 | -0.20 | -0.84 | 0.767 | 0.867 | 1.000 | 25209 | tags=43%, list=46%, signal=80% | |
3743 | INTEGRIN ACTIVATION | 17 | -0.33 | -0.84 | 0.632 | 0.867 | 1.000 | 33832 | tags=88%, list=62%, signal=231% | |
3744 | CILIUM ORGANIZATION | 321 | -0.25 | -0.84 | 0.639 | 0.867 | 1.000 | 34467 | tags=75%, list=63%, signal=201% | |
3745 | POSITIVE REGULATION OF NITRIC-OXIDE SYNTHASE ACTIVITY | 41 | -0.25 | -0.84 | 0.680 | 0.867 | 1.000 | 12819 | tags=27%, list=23%, signal=35% | |
3746 | L-PHENYLALANINE METABOLIC PROCESS | 27 | -0.26 | -0.84 | 0.709 | 0.867 | 1.000 | 27511 | tags=52%, list=50%, signal=104% | |
3747 | L-PHENYLALANINE CATABOLIC PROCESS | 27 | -0.26 | -0.84 | 0.709 | 0.867 | 1.000 | 27511 | tags=52%, list=50%, signal=104% | |
3748 | ERYTHROSE 4-PHOSPHATE/PHOSPHOENOLPYRUVATE FAMILY AMINO ACID METABOLIC PROCESS | 27 | -0.26 | -0.84 | 0.709 | 0.866 | 1.000 | 27511 | tags=52%, list=50%, signal=104% | |
3749 | ERYTHROSE 4-PHOSPHATE/PHOSPHOENOLPYRUVATE FAMILY AMINO ACID CATABOLIC PROCESS | 27 | -0.26 | -0.84 | 0.709 | 0.866 | 1.000 | 27511 | tags=52%, list=50%, signal=104% | |
3750 | REGULATION OF EXTENT OF CELL GROWTH | 98 | -0.21 | -0.84 | 0.740 | 0.866 | 1.000 | 28543 | tags=53%, list=52%, signal=111% | |
3751 | VIRAL ENTRY INTO HOST CELL | 65 | -0.24 | -0.84 | 0.696 | 0.866 | 1.000 | 30175 | tags=68%, list=55%, signal=151% | |
3752 | REGULATION OF APPETITE | 31 | -0.23 | -0.84 | 0.713 | 0.866 | 1.000 | 31909 | tags=61%, list=58%, signal=147% | |
3753 | PEPTIDE TRANSPORT | 77 | -0.22 | -0.84 | 0.738 | 0.866 | 1.000 | 25501 | tags=48%, list=47%, signal=90% | |
3754 | NEGATIVE REGULATION OF ACTIN FILAMENT DEPOLYMERIZATION | 30 | -0.26 | -0.84 | 0.710 | 0.866 | 1.000 | 19184 | tags=40%, list=35%, signal=62% | |
3755 | CEREBELLUM DEVELOPMENT | 43 | -0.24 | -0.84 | 0.701 | 0.866 | 1.000 | 21276 | tags=40%, list=39%, signal=65% | |
3756 | METENCEPHALON DEVELOPMENT | 43 | -0.24 | -0.84 | 0.701 | 0.865 | 1.000 | 21276 | tags=40%, list=39%, signal=65% | |
3757 | HOMOCYSTEINE METABOLIC PROCESS | 19 | -0.28 | -0.84 | 0.671 | 0.865 | 1.000 | 18055 | tags=37%, list=33%, signal=55% | |
3758 | CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 26 | -0.28 | -0.84 | 0.651 | 0.866 | 1.000 | 23098 | tags=54%, list=42%, signal=93% | |
3759 | REGULATION OF NON-CANONICAL WNT SIGNALING PATHWAY | 37 | -0.25 | -0.84 | 0.665 | 0.866 | 1.000 | 23725 | tags=51%, list=43%, signal=91% | |
3760 | SOMATOSTATIN RECEPTOR SIGNALING PATHWAY | 9 | -0.33 | -0.84 | 0.653 | 0.866 | 1.000 | 6157 | tags=22%, list=11%, signal=25% | |
3761 | SOMATOSTATIN SIGNALING PATHWAY | 9 | -0.33 | -0.84 | 0.653 | 0.866 | 1.000 | 6157 | tags=22%, list=11%, signal=25% | |
3762 | EMBRYONIC ORGAN MORPHOGENESIS | 227 | -0.19 | -0.84 | 0.798 | 0.866 | 1.000 | 31192 | tags=55%, list=57%, signal=128% | |
3763 | REGULATION OF PH | 92 | -0.23 | -0.84 | 0.704 | 0.866 | 1.000 | 14847 | tags=33%, list=27%, signal=45% | |
3764 | RESPONSE TO VITAMIN | 34 | -0.27 | -0.84 | 0.728 | 0.866 | 1.000 | 28737 | tags=68%, list=53%, signal=143% | |
3765 | NEGATIVE REGULATION OF CATENIN IMPORT INTO NUCLEUS | 18 | -0.29 | -0.84 | 0.680 | 0.865 | 1.000 | 27997 | tags=44%, list=51%, signal=91% | |
3766 | REGULATION OF ANION TRANSMEMBRANE TRANSPORT | 54 | -0.24 | -0.84 | 0.707 | 0.865 | 1.000 | 9383 | tags=24%, list=17%, signal=29% | |
3767 | SKELETAL SYSTEM MORPHOGENESIS | 144 | -0.20 | -0.84 | 0.758 | 0.865 | 1.000 | 31038 | tags=53%, list=57%, signal=122% | |
3768 | PHOSPHATIDYLETHANOLAMINE BIOSYNTHETIC PROCESS | 28 | -0.28 | -0.84 | 0.660 | 0.865 | 1.000 | 30933 | tags=71%, list=57%, signal=164% | |
3769 | GLOMERULAR EPITHELIAL CELL DEVELOPMENT | 16 | -0.29 | -0.84 | 0.682 | 0.865 | 1.000 | 18177 | tags=38%, list=33%, signal=56% | |
3770 | NEGATIVE REGULATION OF CELL GROWTH | 243 | -0.21 | -0.84 | 0.756 | 0.866 | 1.000 | 28867 | tags=53%, list=53%, signal=112% | |
3771 | REGULATION OF CHEMOKINE PRODUCTION | 87 | -0.25 | -0.84 | 0.689 | 0.866 | 1.000 | 19886 | tags=43%, list=36%, signal=67% | |
3772 | RESPONSE TO ARSENIC-CONTAINING SUBSTANCE | 26 | -0.30 | -0.84 | 0.706 | 0.866 | 1.000 | 28588 | tags=65%, list=52%, signal=137% | |
3773 | REGULATION OF FIBROBLAST PROLIFERATION | 115 | -0.21 | -0.83 | 0.765 | 0.866 | 1.000 | 30781 | tags=58%, list=56%, signal=133% | |
3774 | CILIUM MOVEMENT | 35 | -0.30 | -0.83 | 0.633 | 0.866 | 1.000 | 17345 | tags=46%, list=32%, signal=67% | |
3775 | RNA (GUANINE-N7)-METHYLATION | 6 | -0.37 | -0.83 | 0.701 | 0.866 | 1.000 | 27661 | tags=67%, list=51%, signal=135% | |
3776 | REGULATION OF DELAYED RECTIFIER POTASSIUM CHANNEL ACTIVITY | 45 | -0.22 | -0.83 | 0.738 | 0.866 | 1.000 | 25853 | tags=49%, list=47%, signal=93% | |
3777 | REGULATION OF RNA EXPORT FROM NUCLEUS | 31 | -0.29 | -0.83 | 0.653 | 0.866 | 1.000 | 34235 | tags=77%, list=63%, signal=207% | |
3778 | AXON EXTENSION | 41 | -0.24 | -0.83 | 0.634 | 0.866 | 1.000 | 16029 | tags=34%, list=29%, signal=48% | |
3779 | POSITIVE REGULATION OF NEURON PROJECTION DEVELOPMENT | 295 | -0.20 | -0.83 | 0.803 | 0.866 | 1.000 | 29312 | tags=54%, list=54%, signal=116% | |
3780 | NEGATIVE REGULATION OF GLIOGENESIS | 35 | -0.24 | -0.83 | 0.749 | 0.866 | 1.000 | 22891 | tags=43%, list=42%, signal=74% | |
3781 | SALIVARY GLAND DEVELOPMENT | 24 | -0.28 | -0.83 | 0.637 | 0.866 | 1.000 | 21813 | tags=42%, list=40%, signal=69% | |
3782 | ORGAN MATURATION | 30 | -0.25 | -0.83 | 0.701 | 0.866 | 1.000 | 20764 | tags=33%, list=38%, signal=54% | |
3783 | REGULATION OF HISTONE DEACETYLASE ACTIVITY | 24 | -0.29 | -0.83 | 0.665 | 0.867 | 1.000 | 27706 | tags=67%, list=51%, signal=135% | |
3784 | REGULATION OF OXIDATIVE STRESS-INDUCED NEURON INTRINSIC APOPTOTIC SIGNALING PATHWAY | 19 | -0.30 | -0.83 | 0.692 | 0.867 | 1.000 | 34370 | tags=84%, list=63%, signal=227% | |
3785 | VENTRICULAR SYSTEM DEVELOPMENT | 24 | -0.29 | -0.83 | 0.655 | 0.867 | 1.000 | 22036 | tags=54%, list=40%, signal=91% | |
3786 | POTASSIUM ION EXPORT | 16 | -0.28 | -0.83 | 0.686 | 0.866 | 1.000 | 15903 | tags=31%, list=29%, signal=44% | |
3787 | NEGATIVE REGULATION OF DNA BINDING | 83 | -0.23 | -0.83 | 0.707 | 0.866 | 1.000 | 36193 | tags=71%, list=66%, signal=210% | |
3788 | SPLICEOSOMAL COMPLEX ASSEMBLY | 85 | -0.27 | -0.83 | 0.658 | 0.866 | 1.000 | 31450 | tags=69%, list=58%, signal=163% | |
3789 | NEGATIVE REGULATION OF STEROL TRANSPORT | 21 | -0.31 | -0.83 | 0.655 | 0.867 | 1.000 | 19183 | tags=43%, list=35%, signal=66% | |
3790 | NEGATIVE REGULATION OF CHOLESTEROL TRANSPORT | 21 | -0.31 | -0.83 | 0.655 | 0.866 | 1.000 | 19183 | tags=43%, list=35%, signal=66% | |
3791 | REGULATION OF HEART MORPHOGENESIS | 30 | -0.25 | -0.83 | 0.663 | 0.866 | 1.000 | 23703 | tags=47%, list=43%, signal=82% | |
3792 | MULTICELLULAR ORGANISMAL AGING | 14 | -0.32 | -0.83 | 0.632 | 0.866 | 1.000 | 18032 | tags=50%, list=33%, signal=75% | |
3793 | NEGATIVE REGULATION OF IMMUNE SYSTEM PROCESS | 514 | -0.21 | -0.83 | 0.733 | 0.866 | 1.000 | 22598 | tags=41%, list=41%, signal=69% | |
3794 | NEGATIVE REGULATION OF PHAGOCYTOSIS | 11 | -0.37 | -0.83 | 0.688 | 0.866 | 1.000 | 19886 | tags=55%, list=36%, signal=86% | |
3795 | POSITIVE REGULATION OF CELL MOTILITY | 700 | -0.20 | -0.83 | 0.814 | 0.866 | 1.000 | 31064 | tags=56%, list=57%, signal=127% | |
3796 | PROTEIN KINASE C-ACTIVATING G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 20 | -0.29 | -0.83 | 0.718 | 0.866 | 1.000 | 6018 | tags=25%, list=11%, signal=28% | |
3797 | PH REDUCTION | 48 | -0.25 | -0.83 | 0.655 | 0.866 | 1.000 | 31207 | tags=67%, list=57%, signal=155% | |
3798 | MULTICELLULAR ORGANISMAL IRON ION HOMEOSTASIS | 17 | -0.30 | -0.83 | 0.645 | 0.866 | 1.000 | 17837 | tags=47%, list=33%, signal=70% | |
3799 | EMBRYONIC CAMERA-TYPE EYE FORMATION | 18 | -0.28 | -0.83 | 0.729 | 0.866 | 1.000 | 19696 | tags=44%, list=36%, signal=69% | |
3800 | POSITIVE REGULATION OF CALCIUM-MEDIATED SIGNALING | 28 | -0.27 | -0.83 | 0.706 | 0.866 | 1.000 | 22671 | tags=46%, list=41%, signal=79% | |
3801 | NEGATIVE REGULATION OF MACROPHAGE DERIVED FOAM CELL DIFFERENTIATION | 32 | -0.27 | -0.83 | 0.705 | 0.865 | 1.000 | 37449 | tags=84%, list=68%, signal=268% | |
3802 | SENSORY PERCEPTION OF SMELL | 40 | -0.25 | -0.83 | 0.698 | 0.865 | 1.000 | 11969 | tags=25%, list=22%, signal=32% | |
3803 | REGULATION OF FATTY ACID TRANSPORT | 40 | -0.26 | -0.83 | 0.672 | 0.865 | 1.000 | 28880 | tags=60%, list=53%, signal=127% | |
3804 | NITRIC OXIDE BIOSYNTHETIC PROCESS | 24 | -0.26 | -0.83 | 0.661 | 0.865 | 1.000 | 11503 | tags=33%, list=21%, signal=42% | |
3805 | CENTRAL NERVOUS SYSTEM NEURON AXONOGENESIS | 49 | -0.23 | -0.83 | 0.698 | 0.866 | 1.000 | 23136 | tags=47%, list=42%, signal=81% | |
3806 | FACE MORPHOGENESIS | 37 | -0.25 | -0.83 | 0.692 | 0.866 | 1.000 | 14053 | tags=30%, list=26%, signal=40% | |
3807 | T CELL HOMEOSTASIS | 14 | -0.30 | -0.83 | 0.727 | 0.866 | 1.000 | 30021 | tags=64%, list=55%, signal=143% | |
3808 | RESPONSE TO STEROL | 47 | -0.24 | -0.83 | 0.719 | 0.866 | 1.000 | 19257 | tags=38%, list=35%, signal=59% | |
3809 | RESPONSE TO ALKALOID | 66 | -0.24 | -0.83 | 0.690 | 0.866 | 1.000 | 17667 | tags=32%, list=32%, signal=47% | |
3810 | NEURONAL STEM CELL POPULATION MAINTENANCE | 29 | -0.25 | -0.83 | 0.712 | 0.866 | 1.000 | 30955 | tags=62%, list=57%, signal=143% | |
3811 | APOPTOTIC PROCESS INVOLVED IN DEVELOPMENT | 17 | -0.29 | -0.83 | 0.695 | 0.866 | 1.000 | 4356 | tags=18%, list=8%, signal=19% | |
3812 | HISTONE H4-K16 ACETYLATION | 44 | -0.26 | -0.83 | 0.676 | 0.866 | 1.000 | 13935 | tags=34%, list=25%, signal=46% | |
3813 | HEAD MORPHOGENESIS | 40 | -0.25 | -0.83 | 0.694 | 0.866 | 1.000 | 14053 | tags=30%, list=26%, signal=40% | |
3814 | REGULATION OF MEGAKARYOCYTE DIFFERENTIATION | 39 | -0.24 | -0.83 | 0.701 | 0.866 | 1.000 | 34220 | tags=72%, list=63%, signal=192% | |
3815 | HYALURONAN CATABOLIC PROCESS | 37 | -0.27 | -0.83 | 0.637 | 0.866 | 1.000 | 20622 | tags=46%, list=38%, signal=74% | |
3816 | RESPONSE TO KETONE | 105 | -0.21 | -0.83 | 0.777 | 0.866 | 1.000 | 11900 | tags=23%, list=22%, signal=29% | |
3817 | NEGATIVE REGULATION OF POTASSIUM ION TRANSPORT | 47 | -0.21 | -0.83 | 0.715 | 0.867 | 1.000 | 25853 | tags=49%, list=47%, signal=93% | |
3818 | EAR MORPHOGENESIS | 71 | -0.22 | -0.83 | 0.729 | 0.867 | 1.000 | 30361 | tags=54%, list=56%, signal=120% | |
3819 | NEUROTRANSMITTER BIOSYNTHETIC PROCESS | 25 | -0.24 | -0.83 | 0.729 | 0.867 | 1.000 | 9583 | tags=24%, list=18%, signal=29% | |
3820 | REGULATION OF SISTER CHROMATID COHESION | 35 | -0.27 | -0.83 | 0.671 | 0.867 | 1.000 | 24486 | tags=51%, list=45%, signal=93% | |
3821 | POSITIVE REGULATION OF HISTONE H3-K4 METHYLATION | 40 | -0.28 | -0.83 | 0.690 | 0.867 | 1.000 | 31667 | tags=70%, list=58%, signal=166% | |
3822 | RENAL SYSTEM PROCESS | 203 | -0.20 | -0.83 | 0.738 | 0.868 | 1.000 | 22200 | tags=39%, list=41%, signal=65% | |
3823 | PROTEIN LOCALIZATION TO CILIUM | 34 | -0.29 | -0.83 | 0.702 | 0.868 | 1.000 | 36501 | tags=88%, list=67%, signal=265% | |
3824 | REGULATION OF CELL ADHESION | 1075 | -0.20 | -0.83 | 0.788 | 0.868 | 1.000 | 30255 | tags=55%, list=55%, signal=121% | |
3825 | PROTEIN COMPLEX LOCALIZATION | 72 | -0.27 | -0.83 | 0.626 | 0.868 | 1.000 | 27695 | tags=64%, list=51%, signal=129% | |
3826 | REGULATION OF INTERLEUKIN-12 SECRETION | 18 | -0.27 | -0.83 | 0.684 | 0.868 | 1.000 | 19607 | tags=44%, list=36%, signal=69% | |
3827 | PEPTIDYL-THREONINE PHOSPHORYLATION | 121 | -0.22 | -0.83 | 0.685 | 0.869 | 1.000 | 18140 | tags=38%, list=33%, signal=57% | |
3828 | NEGATIVE REGULATION OF TUMOR NECROSIS FACTOR SUPERFAMILY CYTOKINE PRODUCTION | 70 | -0.25 | -0.83 | 0.696 | 0.869 | 1.000 | 4564 | tags=16%, list=8%, signal=17% | |
3829 | TELENCEPHALON CELL MIGRATION | 48 | -0.25 | -0.83 | 0.691 | 0.869 | 1.000 | 36712 | tags=77%, list=67%, signal=234% | |
3830 | MULTI-ORGANISM REPRODUCTIVE PROCESS | 572 | -0.19 | -0.83 | 0.856 | 0.869 | 1.000 | 21886 | tags=38%, list=40%, signal=62% | |
3831 | PROSTATE GLAND DEVELOPMENT | 19 | -0.29 | -0.83 | 0.673 | 0.869 | 1.000 | 21813 | tags=47%, list=40%, signal=79% | |
3832 | NEGATIVE REGULATION OF SODIUM ION TRANSPORT | 19 | -0.29 | -0.83 | 0.648 | 0.870 | 1.000 | 16488 | tags=42%, list=30%, signal=60% | |
3833 | NEGATIVE REGULATION OF SODIUM ION TRANSMEMBRANE TRANSPORT | 19 | -0.29 | -0.83 | 0.648 | 0.869 | 1.000 | 16488 | tags=42%, list=30%, signal=60% | |
3834 | POSITIVE REGULATION OF TYPE 2 IMMUNE RESPONSE | 17 | -0.30 | -0.83 | 0.666 | 0.871 | 1.000 | 14123 | tags=29%, list=26%, signal=40% | |
3835 | POSITIVE REGULATION OF EPITHELIAL CELL MIGRATION | 249 | -0.20 | -0.83 | 0.795 | 0.871 | 1.000 | 20259 | tags=37%, list=37%, signal=58% | |
3836 | AROMATIC AMINO ACID TRANSPORT | 6 | -0.41 | -0.83 | 0.660 | 0.871 | 1.000 | 17929 | tags=50%, list=33%, signal=74% | |
3837 | MELANOSOME ORGANIZATION | 20 | -0.29 | -0.83 | 0.704 | 0.871 | 1.000 | 25589 | tags=65%, list=47%, signal=122% | |
3838 | PIGMENT GRANULE ORGANIZATION | 20 | -0.29 | -0.83 | 0.704 | 0.870 | 1.000 | 25589 | tags=65%, list=47%, signal=122% | |
3839 | NEGATIVE REGULATION OF OXIDOREDUCTASE ACTIVITY | 34 | -0.25 | -0.83 | 0.662 | 0.870 | 1.000 | 14822 | tags=32%, list=27%, signal=44% | |
3840 | NUCLEOSIDE BISPHOSPHATE METABOLIC PROCESS | 55 | -0.23 | -0.83 | 0.727 | 0.870 | 1.000 | 37182 | tags=82%, list=68%, signal=255% | |
3841 | RIBONUCLEOSIDE BISPHOSPHATE METABOLIC PROCESS | 55 | -0.23 | -0.83 | 0.727 | 0.870 | 1.000 | 37182 | tags=82%, list=68%, signal=255% | |
3842 | PURINE NUCLEOSIDE BISPHOSPHATE METABOLIC PROCESS | 55 | -0.23 | -0.83 | 0.727 | 0.870 | 1.000 | 37182 | tags=82%, list=68%, signal=255% | |
3843 | REGULATION OF PROTEIN KINASE C SIGNALING | 26 | -0.26 | -0.83 | 0.734 | 0.870 | 1.000 | 35029 | tags=77%, list=64%, signal=214% | |
3844 | REGULATION OF ORGANIC ACID TRANSPORT | 48 | -0.25 | -0.83 | 0.688 | 0.869 | 1.000 | 26493 | tags=54%, list=48%, signal=105% | |
3845 | CELL COMMUNICATION BY ELECTRICAL COUPLING | 33 | -0.25 | -0.83 | 0.710 | 0.869 | 1.000 | 22870 | tags=42%, list=42%, signal=73% | |
3846 | INTERLEUKIN-1-MEDIATED SIGNALING PATHWAY | 28 | -0.26 | -0.83 | 0.669 | 0.869 | 1.000 | 14239 | tags=32%, list=26%, signal=43% | |
3847 | REGULATION OF CELL-CELL ADHESION | 622 | -0.20 | -0.83 | 0.782 | 0.869 | 1.000 | 23957 | tags=43%, list=44%, signal=76% | |
3848 | HEART MORPHOGENESIS | 287 | -0.19 | -0.83 | 0.845 | 0.869 | 1.000 | 32149 | tags=57%, list=59%, signal=137% | |
3849 | POSITIVE REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 57 | -0.24 | -0.82 | 0.688 | 0.869 | 1.000 | 30219 | tags=56%, list=55%, signal=125% | |
3850 | NEGATIVE REGULATION OF DNA-DEPENDENT DNA REPLICATION | 31 | -0.27 | -0.82 | 0.701 | 0.869 | 1.000 | 27915 | tags=58%, list=51%, signal=119% | |
3851 | RESPIRATORY BURST | 30 | -0.28 | -0.82 | 0.630 | 0.869 | 1.000 | 15420 | tags=40%, list=28%, signal=56% | |
3852 | PHOTORECEPTOR CELL MAINTENANCE | 48 | -0.23 | -0.82 | 0.696 | 0.869 | 1.000 | 25269 | tags=48%, list=46%, signal=89% | |
3853 | REGULATION OF INTERLEUKIN-12 PRODUCTION | 93 | -0.24 | -0.82 | 0.717 | 0.869 | 1.000 | 20018 | tags=42%, list=37%, signal=66% | |
3854 | POSITIVE REGULATION OF CELL MIGRATION | 685 | -0.19 | -0.82 | 0.832 | 0.869 | 1.000 | 31064 | tags=56%, list=57%, signal=128% | |
3855 | NEGATIVE REGULATION OF DEVELOPMENTAL PROCESS | 1137 | -0.19 | -0.82 | 0.860 | 0.870 | 1.000 | 29204 | tags=52%, list=53%, signal=109% | |
3856 | NEGATIVE REGULATION OF ORGANIC ACID TRANSPORT | 27 | -0.26 | -0.82 | 0.698 | 0.870 | 1.000 | 34905 | tags=78%, list=64%, signal=215% | |
3857 | REGULATION OF MESENCHYMAL STEM CELL DIFFERENTIATION | 23 | -0.27 | -0.82 | 0.715 | 0.870 | 1.000 | 7817 | tags=22%, list=14%, signal=25% | |
3858 | CELLULAR COMPONENT ASSEMBLY INVOLVED IN MORPHOGENESIS | 404 | -0.23 | -0.82 | 0.663 | 0.870 | 1.000 | 34624 | tags=72%, list=63%, signal=194% | |
3859 | NEGATIVE REGULATION OF PEPTIDYL-TYROSINE PHOSPHORYLATION | 76 | -0.23 | -0.82 | 0.723 | 0.870 | 1.000 | 28934 | tags=58%, list=53%, signal=123% | |
3860 | REGULATION OF CELL MOTILITY | 1228 | -0.19 | -0.82 | 0.838 | 0.870 | 1.000 | 30255 | tags=54%, list=55%, signal=119% | |
3861 | REGULATION OF CELL MIGRATION | 1166 | -0.19 | -0.82 | 0.830 | 0.871 | 1.000 | 29073 | tags=52%, list=53%, signal=109% | |
3862 | NEGATIVE REGULATION OF MYELOID CELL DIFFERENTIATION | 116 | -0.22 | -0.82 | 0.726 | 0.871 | 1.000 | 34080 | tags=63%, list=62%, signal=167% | |
3863 | POSITIVE REGULATION OF GLYCOGEN BIOSYNTHETIC PROCESS | 36 | -0.23 | -0.82 | 0.749 | 0.872 | 1.000 | 12145 | tags=25%, list=22%, signal=32% | |
3864 | POSITIVE REGULATION OF GLYCOPROTEIN METABOLIC PROCESS | 40 | -0.26 | -0.82 | 0.738 | 0.872 | 1.000 | 25712 | tags=55%, list=47%, signal=104% | |
3865 | SKELETAL MYOFIBRIL ASSEMBLY | 31 | -0.26 | -0.82 | 0.678 | 0.872 | 1.000 | 18530 | tags=45%, list=34%, signal=68% | |
3866 | NERVE DEVELOPMENT | 64 | -0.21 | -0.82 | 0.720 | 0.873 | 1.000 | 34193 | tags=67%, list=63%, signal=179% | |
3867 | NEGATIVE REGULATION OF PEPTIDE SECRETION | 32 | -0.24 | -0.82 | 0.715 | 0.873 | 1.000 | 13452 | tags=28%, list=25%, signal=37% | |
3868 | POSITIVE REGULATION OF ACTIN FILAMENT DEPOLYMERIZATION | 29 | -0.26 | -0.82 | 0.738 | 0.873 | 1.000 | 32761 | tags=72%, list=60%, signal=181% | |
3869 | HOMOPHILIC CELL ADHESION VIA PLASMA MEMBRANE ADHESION MOLECULES | 78 | -0.22 | -0.82 | 0.761 | 0.873 | 1.000 | 21586 | tags=40%, list=39%, signal=66% | |
3870 | PIGMENTATION | 100 | -0.23 | -0.82 | 0.772 | 0.873 | 1.000 | 28128 | tags=58%, list=51%, signal=119% | |
3871 | CEREBRAL CORTEX CELL MIGRATION | 40 | -0.26 | -0.82 | 0.669 | 0.873 | 1.000 | 36427 | tags=78%, list=67%, signal=232% | |
3872 | REGULATION OF INTRACELLULAR PH | 75 | -0.23 | -0.82 | 0.727 | 0.873 | 1.000 | 31207 | tags=63%, list=57%, signal=146% | |
3873 | EPITHELIAL CELL PROLIFERATION | 98 | -0.20 | -0.82 | 0.806 | 0.873 | 1.000 | 30585 | tags=56%, list=56%, signal=127% | |
3874 | SENSORY PERCEPTION OF SOUND | 165 | -0.20 | -0.82 | 0.766 | 0.873 | 1.000 | 24433 | tags=42%, list=45%, signal=75% | |
3875 | NEURON FATE COMMITMENT | 26 | -0.25 | -0.82 | 0.702 | 0.873 | 1.000 | 35657 | tags=81%, list=65%, signal=232% | |
3876 | REGULATION OF KIDNEY DEVELOPMENT | 84 | -0.22 | -0.82 | 0.694 | 0.874 | 1.000 | 19886 | tags=38%, list=36%, signal=60% | |
3877 | INTRACELLULAR PH REDUCTION | 45 | -0.25 | -0.82 | 0.673 | 0.874 | 1.000 | 31207 | tags=67%, list=57%, signal=155% | |
3878 | CELLULAR PROCESS INVOLVED IN REPRODUCTION IN MULTICELLULAR ORGANISM | 149 | -0.19 | -0.82 | 0.795 | 0.874 | 1.000 | 21263 | tags=37%, list=39%, signal=60% | |
3879 | MICROTUBULE ANCHORING | 39 | -0.27 | -0.82 | 0.684 | 0.874 | 1.000 | 35584 | tags=82%, list=65%, signal=235% | |
3880 | HYDROGEN PEROXIDE CATABOLIC PROCESS | 31 | -0.30 | -0.82 | 0.660 | 0.874 | 1.000 | 15100 | tags=39%, list=28%, signal=53% | |
3881 | RESPONSE TO MANGANESE ION | 9 | -0.32 | -0.82 | 0.683 | 0.874 | 1.000 | 35255 | tags=89%, list=64%, signal=250% | |
3882 | CITRULLINE METABOLIC PROCESS | 17 | -0.28 | -0.82 | 0.700 | 0.874 | 1.000 | 21711 | tags=47%, list=40%, signal=78% | |
3883 | REGULATION OF ANATOMICAL STRUCTURE SIZE | 489 | -0.19 | -0.82 | 0.825 | 0.874 | 1.000 | 19452 | tags=36%, list=36%, signal=55% | |
3884 | AXONEME ASSEMBLY | 60 | -0.27 | -0.82 | 0.643 | 0.873 | 1.000 | 34039 | tags=78%, list=62%, signal=207% | |
3885 | POSITIVE REGULATION OF OXIDATIVE STRESS-INDUCED CELL DEATH | 19 | -0.29 | -0.82 | 0.704 | 0.873 | 1.000 | 6539 | tags=26%, list=12%, signal=30% | |
3886 | POSITIVE REGULATION OF NEURON DIFFERENTIATION | 375 | -0.19 | -0.82 | 0.834 | 0.874 | 1.000 | 29312 | tags=53%, list=54%, signal=114% | |
3887 | MESENCHYMAL CELL DIFFERENTIATION | 163 | -0.19 | -0.82 | 0.769 | 0.875 | 1.000 | 28154 | tags=49%, list=51%, signal=101% | |
3888 | POSITIVE REGULATION OF CELL DIFFERENTIATION | 1239 | -0.19 | -0.82 | 0.847 | 0.874 | 1.000 | 30991 | tags=55%, list=57%, signal=123% | |
3889 | CYTOKINE SECRETION | 65 | -0.26 | -0.82 | 0.716 | 0.874 | 1.000 | 25375 | tags=55%, list=46%, signal=103% | |
3890 | NEGATIVE REGULATION OF DNA RECOMBINATION | 23 | -0.28 | -0.82 | 0.738 | 0.874 | 1.000 | 21204 | tags=48%, list=39%, signal=78% | |
3891 | CHEMOKINE PRODUCTION | 17 | -0.29 | -0.82 | 0.715 | 0.876 | 1.000 | 19607 | tags=47%, list=36%, signal=73% | |
3892 | MONOVALENT INORGANIC CATION HOMEOSTASIS | 141 | -0.21 | -0.82 | 0.769 | 0.875 | 1.000 | 27044 | tags=51%, list=49%, signal=101% | |
3893 | CELLULAR LACTAM METABOLIC PROCESS | 10 | -0.37 | -0.82 | 0.715 | 0.877 | 1.000 | 27510 | tags=70%, list=50%, signal=141% | |
3894 | EYELID DEVELOPMENT IN CAMERA-TYPE EYE | 14 | -0.30 | -0.82 | 0.719 | 0.877 | 1.000 | 35937 | tags=86%, list=66%, signal=250% | |
3895 | CALCIUM-MEDIATED SIGNALING USING INTRACELLULAR CALCIUM SOURCE | 17 | -0.29 | -0.82 | 0.709 | 0.877 | 1.000 | 17523 | tags=41%, list=32%, signal=61% | |
3896 | POSITIVE REGULATION OF RECEPTOR INTERNALIZATION | 41 | -0.26 | -0.82 | 0.725 | 0.877 | 1.000 | 28190 | tags=59%, list=52%, signal=121% | |
3897 | CILIUM ASSEMBLY | 302 | -0.24 | -0.82 | 0.667 | 0.877 | 1.000 | 34467 | tags=74%, list=63%, signal=198% | |
3898 | DNA STRAND RENATURATION | 18 | -0.28 | -0.82 | 0.684 | 0.877 | 1.000 | 27841 | tags=61%, list=51%, signal=124% | |
3899 | REGULATION OF DNA-DEPENDENT DNA REPLICATION | 67 | -0.25 | -0.81 | 0.723 | 0.878 | 1.000 | 34159 | tags=70%, list=62%, signal=187% | |
3900 | AROMATIC AMINO ACID FAMILY CATABOLIC PROCESS | 43 | -0.25 | -0.81 | 0.699 | 0.878 | 1.000 | 28232 | tags=53%, list=52%, signal=111% | |
3901 | CEREBELLAR CORTEX DEVELOPMENT | 31 | -0.24 | -0.81 | 0.719 | 0.878 | 1.000 | 21276 | tags=42%, list=39%, signal=69% | |
3902 | ANATOMICAL STRUCTURE FORMATION INVOLVED IN MORPHOGENESIS | 1149 | -0.19 | -0.81 | 0.871 | 0.878 | 1.000 | 34492 | tags=64%, list=63%, signal=170% | |
3903 | MICROTUBULE NUCLEATION | 35 | -0.28 | -0.81 | 0.678 | 0.878 | 1.000 | 33722 | tags=80%, list=62%, signal=209% | |
3904 | NEGATIVE REGULATION OF INTERLEUKIN-2 PRODUCTION | 33 | -0.24 | -0.81 | 0.744 | 0.878 | 1.000 | 9311 | tags=21%, list=17%, signal=26% | |
3905 | VENTRICULAR CARDIAC MUSCLE CELL DEVELOPMENT | 11 | -0.32 | -0.81 | 0.688 | 0.879 | 1.000 | 23708 | tags=64%, list=43%, signal=112% | |
3906 | NEGATIVE REGULATION OF ADAPTIVE IMMUNE RESPONSE BASED ON SOMATIC RECOMBINATION OF IMMUNE RECEPTORS BUILT FROM IMMUNOGLOBULIN SUPERFAMILY DOMAINS | 51 | -0.27 | -0.81 | 0.747 | 0.878 | 1.000 | 7049 | tags=20%, list=13%, signal=22% | |
3907 | NEGATIVE REGULATION OF CELL DIFFERENTIATION | 791 | -0.19 | -0.81 | 0.864 | 0.879 | 1.000 | 30152 | tags=54%, list=55%, signal=118% | |
3908 | REGULATION OF PEPTIDYL-TYROSINE PHOSPHORYLATION | 364 | -0.19 | -0.81 | 0.756 | 0.879 | 1.000 | 28934 | tags=50%, list=53%, signal=105% | |
3909 | REGULATION OF CALCIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 133 | -0.19 | -0.81 | 0.840 | 0.879 | 1.000 | 20627 | tags=38%, list=38%, signal=61% | |
3910 | LIPOXIN METABOLIC PROCESS | 15 | -0.33 | -0.81 | 0.662 | 0.879 | 1.000 | 36670 | tags=100%, list=67%, signal=304% | |
3911 | POSITIVE REGULATION OF CELL PROLIFERATION | 1134 | -0.18 | -0.81 | 0.854 | 0.879 | 1.000 | 31100 | tags=55%, list=57%, signal=124% | |
3912 | POSITIVE REGULATION OF STEROID METABOLIC PROCESS | 34 | -0.26 | -0.81 | 0.704 | 0.878 | 1.000 | 16531 | tags=32%, list=30%, signal=46% | |
3913 | CELLULAR MONOVALENT INORGANIC CATION HOMEOSTASIS | 110 | -0.22 | -0.81 | 0.777 | 0.880 | 1.000 | 27044 | tags=52%, list=49%, signal=102% | |
3914 | POSITIVE REGULATION BY HOST OF VIRAL GENOME REPLICATION | 16 | -0.33 | -0.81 | 0.683 | 0.880 | 1.000 | 33347 | tags=81%, list=61%, signal=208% | |
3915 | ENDOCARDIAL CUSHION FORMATION | 16 | -0.27 | -0.81 | 0.721 | 0.880 | 1.000 | 27150 | tags=56%, list=50%, signal=112% | |
3916 | EPITHELIAL CELL DIFFERENTIATION INVOLVED IN KIDNEY DEVELOPMENT | 47 | -0.22 | -0.81 | 0.761 | 0.881 | 1.000 | 28190 | tags=53%, list=52%, signal=110% | |
3917 | FLOOR PLATE DEVELOPMENT | 9 | -0.31 | -0.81 | 0.739 | 0.881 | 1.000 | 28363 | tags=67%, list=52%, signal=139% | |
3918 | PYRIMIDINE RIBONUCLEOSIDE METABOLIC PROCESS | 25 | -0.26 | -0.81 | 0.727 | 0.881 | 1.000 | 19834 | tags=48%, list=36%, signal=75% | |
3919 | MRNA SPLICE SITE SELECTION | 54 | -0.27 | -0.81 | 0.682 | 0.882 | 1.000 | 31450 | tags=70%, list=58%, signal=165% | |
3920 | CYTOPLASMIC MRNA PROCESSING BODY ASSEMBLY | 27 | -0.26 | -0.81 | 0.742 | 0.882 | 1.000 | 20403 | tags=44%, list=37%, signal=71% | |
3921 | NEGATIVE REGULATION OF LIPID TRANSPORT | 56 | -0.24 | -0.81 | 0.720 | 0.881 | 1.000 | 35599 | tags=73%, list=65%, signal=210% | |
3922 | ACTIVATION OF STORE-OPERATED CALCIUM CHANNEL ACTIVITY | 16 | -0.31 | -0.81 | 0.663 | 0.881 | 1.000 | 22210 | tags=56%, list=41%, signal=95% | |
3923 | POSITIVE REGULATION OF STORE-OPERATED CALCIUM CHANNEL ACTIVITY | 16 | -0.31 | -0.81 | 0.663 | 0.881 | 1.000 | 22210 | tags=56%, list=41%, signal=95% | |
3924 | CELLULAR RESPONSE TO INTERLEUKIN-4 | 25 | -0.27 | -0.81 | 0.696 | 0.881 | 1.000 | 21567 | tags=40%, list=39%, signal=66% | |
3925 | NUCLEOSIDE BISPHOSPHATE BIOSYNTHETIC PROCESS | 19 | -0.27 | -0.81 | 0.688 | 0.881 | 1.000 | 32422 | tags=79%, list=59%, signal=194% | |
3926 | RIBONUCLEOSIDE BISPHOSPHATE BIOSYNTHETIC PROCESS | 19 | -0.27 | -0.81 | 0.688 | 0.881 | 1.000 | 32422 | tags=79%, list=59%, signal=194% | |
3927 | PURINE NUCLEOSIDE BISPHOSPHATE BIOSYNTHETIC PROCESS | 19 | -0.27 | -0.81 | 0.688 | 0.881 | 1.000 | 32422 | tags=79%, list=59%, signal=194% | |
3928 | MELANOCYTE DIFFERENTIATION | 9 | -0.32 | -0.81 | 0.710 | 0.880 | 1.000 | 4449 | tags=22%, list=8%, signal=24% | |
3929 | PEPTIDYL-TYROSINE PHOSPHORYLATION | 309 | -0.19 | -0.81 | 0.805 | 0.880 | 1.000 | 30999 | tags=55%, list=57%, signal=127% | |
3930 | PEPTIDYL-TYROSINE MODIFICATION | 309 | -0.19 | -0.81 | 0.805 | 0.880 | 1.000 | 30999 | tags=55%, list=57%, signal=127% | |
3931 | REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 97 | -0.21 | -0.81 | 0.772 | 0.880 | 1.000 | 29461 | tags=55%, list=54%, signal=118% | |
3932 | CHOLESTEROL HOMEOSTASIS | 99 | -0.22 | -0.81 | 0.732 | 0.881 | 1.000 | 10308 | tags=22%, list=19%, signal=27% | |
3933 | STEROL HOMEOSTASIS | 99 | -0.22 | -0.81 | 0.732 | 0.880 | 1.000 | 10308 | tags=22%, list=19%, signal=27% | |
3934 | AMINO ACID SALVAGE | 18 | -0.29 | -0.81 | 0.712 | 0.881 | 1.000 | 33577 | tags=78%, list=61%, signal=201% | |
3935 | L-METHIONINE BIOSYNTHETIC PROCESS | 18 | -0.29 | -0.81 | 0.712 | 0.880 | 1.000 | 33577 | tags=78%, list=61%, signal=201% | |
3936 | L-METHIONINE SALVAGE | 18 | -0.29 | -0.81 | 0.712 | 0.880 | 1.000 | 33577 | tags=78%, list=61%, signal=201% | |
3937 | CELLULAR RESPONSE TO INTERLEUKIN-6 | 44 | -0.25 | -0.81 | 0.735 | 0.880 | 1.000 | 32842 | tags=64%, list=60%, signal=159% | |
3938 | REGULATION OF INSULIN SECRETION INVOLVED IN CELLULAR RESPONSE TO GLUCOSE STIMULUS | 54 | -0.23 | -0.81 | 0.712 | 0.880 | 1.000 | 14664 | tags=30%, list=27%, signal=40% | |
3939 | CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 150 | -0.22 | -0.81 | 0.755 | 0.881 | 1.000 | 22653 | tags=43%, list=41%, signal=73% | |
3940 | LYMPH VESSEL DEVELOPMENT | 49 | -0.24 | -0.81 | 0.752 | 0.881 | 1.000 | 18077 | tags=37%, list=33%, signal=55% | |
3941 | REGULATION OF COLLAGEN METABOLIC PROCESS | 34 | -0.23 | -0.81 | 0.798 | 0.881 | 1.000 | 14822 | tags=29%, list=27%, signal=40% | |
3942 | REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 34 | -0.23 | -0.81 | 0.798 | 0.880 | 1.000 | 14822 | tags=29%, list=27%, signal=40% | |
3943 | ODONTOGENESIS | 96 | -0.22 | -0.81 | 0.736 | 0.881 | 1.000 | 34415 | tags=65%, list=63%, signal=174% | |
3944 | POTASSIUM ION HOMEOSTASIS | 21 | -0.27 | -0.81 | 0.718 | 0.881 | 1.000 | 24557 | tags=57%, list=45%, signal=104% | |
3945 | NEGATIVE REGULATION OF LIPID METABOLIC PROCESS | 120 | -0.21 | -0.81 | 0.803 | 0.881 | 1.000 | 29616 | tags=55%, list=54%, signal=120% | |
3946 | REGULATION OF GLIAL CELL DIFFERENTIATION | 51 | -0.24 | -0.81 | 0.728 | 0.882 | 1.000 | 32533 | tags=63%, list=60%, signal=155% | |
3947 | CYTOKINE PRODUCTION | 143 | -0.24 | -0.81 | 0.707 | 0.882 | 1.000 | 25520 | tags=52%, list=47%, signal=97% | |
3948 | DNA-DEPENDENT DNA REPLICATION MAINTENANCE OF FIDELITY | 44 | -0.24 | -0.81 | 0.752 | 0.882 | 1.000 | 33781 | tags=64%, list=62%, signal=166% | |
3949 | POSITIVE REGULATION OF INTERLEUKIN-10 PRODUCTION | 37 | -0.27 | -0.81 | 0.755 | 0.882 | 1.000 | 17597 | tags=41%, list=32%, signal=60% | |
3950 | L-GLUTAMATE TRANSMEMBRANE TRANSPORT | 22 | -0.26 | -0.81 | 0.727 | 0.882 | 1.000 | 31473 | tags=68%, list=58%, signal=161% | |
3951 | RESPONSE TO CALCIUM ION | 184 | -0.20 | -0.81 | 0.837 | 0.882 | 1.000 | 35672 | tags=68%, list=65%, signal=195% | |
3952 | REGULATION OF HOMEOSTATIC PROCESS | 754 | -0.18 | -0.81 | 0.858 | 0.882 | 1.000 | 26088 | tags=46%, list=48%, signal=86% | |
3953 | PROTEIN NITROSYLATION | 13 | -0.31 | -0.81 | 0.696 | 0.882 | 1.000 | 9583 | tags=31%, list=18%, signal=37% | |
3954 | PEPTIDYL-CYSTEINE S-NITROSYLATION | 13 | -0.31 | -0.81 | 0.696 | 0.882 | 1.000 | 9583 | tags=31%, list=18%, signal=37% | |
3955 | SULFUR COMPOUND CATABOLIC PROCESS | 104 | -0.22 | -0.81 | 0.694 | 0.882 | 1.000 | 19133 | tags=39%, list=35%, signal=61% | |
3956 | REGULATION OF LEUKOCYTE DIFFERENTIATION | 260 | -0.20 | -0.81 | 0.754 | 0.882 | 1.000 | 27378 | tags=47%, list=50%, signal=93% | |
3957 | RESPONSE TO MERCURY ION | 9 | -0.32 | -0.81 | 0.741 | 0.882 | 1.000 | 9973 | tags=22%, list=18%, signal=27% | |
3958 | AMYLOID FIBRIL FORMATION | 21 | -0.27 | -0.81 | 0.753 | 0.882 | 1.000 | 31408 | tags=71%, list=57%, signal=168% | |
3959 | ACTIN-MEDIATED CELL CONTRACTION | 131 | -0.20 | -0.81 | 0.758 | 0.882 | 1.000 | 20955 | tags=37%, list=38%, signal=59% | |
3960 | RESPONSE TO ISCHEMIA | 15 | -0.29 | -0.81 | 0.656 | 0.883 | 1.000 | 21623 | tags=53%, list=40%, signal=88% | |
3961 | REGULATION OF ANOIKIS | 66 | -0.22 | -0.81 | 0.764 | 0.883 | 1.000 | 29471 | tags=56%, list=54%, signal=121% | |
3962 | POLYAMINE TRANSPORT | 3 | -0.46 | -0.81 | 0.724 | 0.884 | 1.000 | 29607 | tags=100%, list=54%, signal=218% | |
3963 | GLYCINE METABOLIC PROCESS | 21 | -0.27 | -0.80 | 0.716 | 0.884 | 1.000 | 25109 | tags=52%, list=46%, signal=97% | |
3964 | POSITIVE REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 47 | -0.23 | -0.80 | 0.778 | 0.885 | 1.000 | 11450 | tags=26%, list=21%, signal=32% | |
3965 | CELLULAR RESPONSE TO VITAMIN | 16 | -0.29 | -0.80 | 0.745 | 0.885 | 1.000 | 28737 | tags=69%, list=53%, signal=145% | |
3966 | STEM CELL DEVELOPMENT | 145 | -0.19 | -0.80 | 0.805 | 0.885 | 1.000 | 25277 | tags=43%, list=46%, signal=81% | |
3967 | CARDIAC MUSCLE CELL MYOBLAST DIFFERENTIATION | 24 | -0.27 | -0.80 | 0.713 | 0.885 | 1.000 | 7817 | tags=21%, list=14%, signal=24% | |
3968 | REGULATION OF AXONOGENESIS | 166 | -0.20 | -0.80 | 0.824 | 0.885 | 1.000 | 18901 | tags=36%, list=35%, signal=54% | |
3969 | REGULATION OF NUCLEOBASE-CONTAINING COMPOUND TRANSPORT | 33 | -0.27 | -0.80 | 0.682 | 0.885 | 1.000 | 35285 | tags=79%, list=65%, signal=222% | |
3970 | REGULATION OF CELLULAR RESPONSE TO VASCULAR ENDOTHELIAL GROWTH FACTOR STIMULUS | 25 | -0.28 | -0.80 | 0.671 | 0.885 | 1.000 | 7500 | tags=24%, list=14%, signal=28% | |
3971 | CELL DIFFERENTIATION INVOLVED IN KIDNEY DEVELOPMENT | 59 | -0.22 | -0.80 | 0.754 | 0.884 | 1.000 | 28190 | tags=53%, list=52%, signal=108% | |
3972 | CELLULAR RESPONSE TO COLD | 11 | -0.32 | -0.80 | 0.720 | 0.884 | 1.000 | 19715 | tags=55%, list=36%, signal=85% | |
3973 | CALCIUM-MEDIATED SIGNALING | 147 | -0.20 | -0.80 | 0.821 | 0.884 | 1.000 | 33374 | tags=61%, list=61%, signal=155% | |
3974 | NEGATIVE REGULATION OF NITRIC OXIDE BIOSYNTHETIC PROCESS | 14 | -0.30 | -0.80 | 0.736 | 0.884 | 1.000 | 24638 | tags=50%, list=45%, signal=91% | |
3975 | NEGATIVE REGULATION OF NITRIC OXIDE METABOLIC PROCESS | 14 | -0.30 | -0.80 | 0.736 | 0.884 | 1.000 | 24638 | tags=50%, list=45%, signal=91% | |
3976 | PROTEIN LOCALIZATION TO CENTROSOME | 31 | -0.28 | -0.80 | 0.683 | 0.884 | 1.000 | 35584 | tags=84%, list=65%, signal=240% | |
3977 | REGULATION OF INTERLEUKIN-2 SECRETION | 23 | -0.27 | -0.80 | 0.717 | 0.884 | 1.000 | 7414 | tags=22%, list=14%, signal=25% | |
3978 | CELL MIGRATION | 1070 | -0.19 | -0.80 | 0.837 | 0.884 | 1.000 | 29694 | tags=54%, list=54%, signal=115% | |
3979 | PROTEIN SECRETION | 120 | -0.23 | -0.80 | 0.776 | 0.884 | 1.000 | 25375 | tags=52%, list=46%, signal=96% | |
3980 | POSITIVE REGULATION OF MAST CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 6 | -0.37 | -0.80 | 0.712 | 0.884 | 1.000 | 34401 | tags=100%, list=63%, signal=270% | |
3981 | POSITIVE REGULATION OF MAST CELL DEGRANULATION | 6 | -0.37 | -0.80 | 0.712 | 0.884 | 1.000 | 34401 | tags=100%, list=63%, signal=270% | |
3982 | REGULATION OF ALPHA-BETA T CELL DIFFERENTIATION | 56 | -0.23 | -0.80 | 0.762 | 0.884 | 1.000 | 16824 | tags=32%, list=31%, signal=46% | |
3983 | LEUKOCYTE DEGRANULATION | 27 | -0.29 | -0.80 | 0.693 | 0.884 | 1.000 | 22018 | tags=48%, list=40%, signal=81% | |
3984 | IN UTERO EMBRYONIC DEVELOPMENT | 98 | -0.20 | -0.80 | 0.794 | 0.885 | 1.000 | 25567 | tags=47%, list=47%, signal=88% | |
3985 | INTERMEDIATE FILAMENT-BASED PROCESS | 61 | -0.21 | -0.80 | 0.787 | 0.885 | 1.000 | 25778 | tags=43%, list=47%, signal=81% | |
3986 | INTERMEDIATE FILAMENT CYTOSKELETON ORGANIZATION | 61 | -0.21 | -0.80 | 0.787 | 0.885 | 1.000 | 25778 | tags=43%, list=47%, signal=81% | |
3987 | NEGATIVE REGULATION BY HOST OF VIRAL GENOME REPLICATION | 16 | -0.28 | -0.80 | 0.730 | 0.885 | 1.000 | 33347 | tags=69%, list=61%, signal=176% | |
3988 | REGULATION OF PHOSPHATIDYLINOSITOL 3-KINASE SIGNALING | 156 | -0.20 | -0.80 | 0.734 | 0.885 | 1.000 | 22664 | tags=40%, list=41%, signal=68% | |
3989 | POSITIVE REGULATION OF ERK1 AND ERK2 CASCADE | 241 | -0.20 | -0.80 | 0.781 | 0.886 | 1.000 | 31126 | tags=53%, list=57%, signal=123% | |
3990 | TISSUE HOMEOSTASIS | 205 | -0.20 | -0.80 | 0.811 | 0.886 | 1.000 | 24273 | tags=41%, list=44%, signal=73% | |
3991 | REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 187 | -0.21 | -0.80 | 0.803 | 0.886 | 1.000 | 11820 | tags=26%, list=22%, signal=33% | |
3992 | HETEROCHROMATIN ASSEMBLY | 23 | -0.25 | -0.80 | 0.758 | 0.887 | 1.000 | 23888 | tags=48%, list=44%, signal=85% | |
3993 | REGULATION OF INTERFERON-GAMMA-MEDIATED SIGNALING PATHWAY | 55 | -0.24 | -0.80 | 0.720 | 0.887 | 1.000 | 23799 | tags=49%, list=44%, signal=87% | |
3994 | INTRACELLULAR ESTROGEN RECEPTOR SIGNALING PATHWAY | 37 | -0.24 | -0.80 | 0.741 | 0.888 | 1.000 | 19277 | tags=38%, list=35%, signal=58% | |
3995 | NEGATIVE REGULATION OF CENTROSOME DUPLICATION | 24 | -0.28 | -0.80 | 0.696 | 0.888 | 1.000 | 25404 | tags=58%, list=46%, signal=109% | |
3996 | NEGATIVE REGULATION OF CENTROSOME CYCLE | 24 | -0.28 | -0.80 | 0.696 | 0.888 | 1.000 | 25404 | tags=58%, list=46%, signal=109% | |
3997 | DENDRITIC SPINE DEVELOPMENT | 37 | -0.23 | -0.80 | 0.760 | 0.888 | 1.000 | 29821 | tags=62%, list=55%, signal=137% | |
3998 | LEUKOCYTE HOMEOSTASIS | 34 | -0.28 | -0.80 | 0.738 | 0.888 | 1.000 | 27744 | tags=59%, list=51%, signal=119% | |
3999 | REGULATION OF ESTABLISHMENT OR MAINTENANCE OF CELL POLARITY | 44 | -0.24 | -0.80 | 0.712 | 0.888 | 1.000 | 29484 | tags=61%, list=54%, signal=133% | |
4000 | LEUKOCYTE ACTIVATION INVOLVED IN IMMUNE RESPONSE | 148 | -0.21 | -0.80 | 0.768 | 0.888 | 1.000 | 20339 | tags=39%, list=37%, signal=61% | |
4001 | RETINOL METABOLIC PROCESS | 24 | -0.26 | -0.80 | 0.702 | 0.888 | 1.000 | 5820 | tags=21%, list=11%, signal=23% | |
4002 | PROTEIN O-LINKED GLYCOSYLATION | 213 | -0.19 | -0.80 | 0.824 | 0.888 | 1.000 | 25708 | tags=45%, list=47%, signal=85% | |
4003 | IMMUNOGLOBULIN PRODUCTION INVOLVED IN IMMUNOGLOBULIN MEDIATED IMMUNE RESPONSE | 39 | -0.26 | -0.80 | 0.704 | 0.888 | 1.000 | 26403 | tags=56%, list=48%, signal=109% | |
4004 | HOMOTYPIC CELL-CELL ADHESION | 348 | -0.21 | -0.80 | 0.744 | 0.888 | 1.000 | 20622 | tags=39%, list=38%, signal=62% | |
4005 | STEM CELL DIFFERENTIATION | 229 | -0.19 | -0.80 | 0.827 | 0.889 | 1.000 | 26275 | tags=45%, list=48%, signal=87% | |
4006 | METANEPHRIC TUBULE DEVELOPMENT | 24 | -0.25 | -0.80 | 0.719 | 0.890 | 1.000 | 17093 | tags=33%, list=31%, signal=48% | |
4007 | METANEPHRIC NEPHRON TUBULE DEVELOPMENT | 24 | -0.25 | -0.80 | 0.719 | 0.890 | 1.000 | 17093 | tags=33%, list=31%, signal=48% | |
4008 | RESPONSE TO METAL ION | 309 | -0.19 | -0.80 | 0.856 | 0.890 | 1.000 | 35672 | tags=67%, list=65%, signal=191% | |
4009 | ANTERIOR/POSTERIOR PATTERN SPECIFICATION | 90 | -0.22 | -0.80 | 0.759 | 0.889 | 1.000 | 15754 | tags=30%, list=29%, signal=42% | |
4010 | MUSCLE CELL CELLULAR HOMEOSTASIS | 23 | -0.26 | -0.80 | 0.759 | 0.889 | 1.000 | 2830 | tags=17%, list=5%, signal=18% | |
4011 | POSITIVE REGULATION OF GLYCOPROTEIN BIOSYNTHETIC PROCESS | 35 | -0.25 | -0.80 | 0.760 | 0.890 | 1.000 | 25712 | tags=54%, list=47%, signal=102% | |
4012 | NEPHRIC DUCT MORPHOGENESIS | 13 | -0.29 | -0.80 | 0.741 | 0.890 | 1.000 | 14059 | tags=31%, list=26%, signal=41% | |
4013 | RESPONSE TO ANTIBIOTIC | 46 | -0.25 | -0.80 | 0.698 | 0.890 | 1.000 | 36296 | tags=78%, list=66%, signal=233% | |
4014 | NEURAL CREST CELL MIGRATION | 30 | -0.23 | -0.80 | 0.771 | 0.890 | 1.000 | 23507 | tags=43%, list=43%, signal=76% | |
4015 | EMBRYO DEVELOPMENT | 753 | -0.18 | -0.80 | 0.900 | 0.890 | 1.000 | 31201 | tags=54%, list=57%, signal=124% | |
4016 | POSITIVE REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 31 | -0.23 | -0.80 | 0.783 | 0.890 | 1.000 | 25822 | tags=48%, list=47%, signal=92% | |
4017 | REPRODUCTION | 891 | -0.17 | -0.80 | 0.931 | 0.890 | 1.000 | 21925 | tags=37%, list=40%, signal=60% | |
4018 | POSITIVE REGULATION OF CELLULAR CARBOHYDRATE METABOLIC PROCESS | 93 | -0.20 | -0.79 | 0.842 | 0.892 | 1.000 | 30219 | tags=55%, list=55%, signal=122% | |
4019 | POSITIVE REGULATION OF TISSUE REMODELING | 24 | -0.27 | -0.79 | 0.724 | 0.892 | 1.000 | 25050 | tags=54%, list=46%, signal=100% | |
4020 | NEGATIVE REGULATION OF HORMONE SECRETION | 45 | -0.25 | -0.79 | 0.741 | 0.891 | 1.000 | 13505 | tags=29%, list=25%, signal=38% | |
4021 | BONE MORPHOGENESIS | 61 | -0.22 | -0.79 | 0.769 | 0.891 | 1.000 | 30361 | tags=56%, list=56%, signal=125% | |
4022 | METANEPHRIC DISTAL TUBULE DEVELOPMENT | 18 | -0.27 | -0.79 | 0.746 | 0.891 | 1.000 | 27646 | tags=50%, list=51%, signal=101% | |
4023 | REGULATION OF RESPONSE TO FOOD | 31 | -0.23 | -0.79 | 0.778 | 0.891 | 1.000 | 31909 | tags=61%, list=58%, signal=147% | |
4024 | REGULATION OF CD4-POSITIVE, ALPHA-BETA T CELL DIFFERENTIATION | 45 | -0.24 | -0.79 | 0.700 | 0.892 | 1.000 | 28398 | tags=49%, list=52%, signal=102% | |
4025 | REGULATION OF TRIGLYCERIDE CATABOLIC PROCESS | 28 | -0.26 | -0.79 | 0.663 | 0.892 | 1.000 | 7644 | tags=21%, list=14%, signal=25% | |
4026 | REPRODUCTIVE PROCESS | 890 | -0.17 | -0.79 | 0.935 | 0.891 | 1.000 | 21925 | tags=37%, list=40%, signal=60% | |
4027 | NEGATIVE REGULATION OF OXIDATIVE STRESS-INDUCED INTRINSIC APOPTOTIC SIGNALING PATHWAY | 34 | -0.27 | -0.79 | 0.738 | 0.891 | 1.000 | 35261 | tags=79%, list=64%, signal=224% | |
4028 | PROTEIN PRENYLATION | 25 | -0.26 | -0.79 | 0.726 | 0.891 | 1.000 | 26269 | tags=52%, list=48%, signal=100% | |
4029 | PRENYLATION | 25 | -0.26 | -0.79 | 0.726 | 0.891 | 1.000 | 26269 | tags=52%, list=48%, signal=100% | |
4030 | REGULATION OF MAST CELL ACTIVATION | 44 | -0.24 | -0.79 | 0.731 | 0.891 | 1.000 | 18565 | tags=36%, list=34%, signal=55% | |
4031 | HINDBRAIN MORPHOGENESIS | 33 | -0.23 | -0.79 | 0.763 | 0.891 | 1.000 | 33770 | tags=67%, list=62%, signal=174% | |
4032 | PROTEIN LOCALIZATION TO CHROMOSOME, TELOMERIC REGION | 34 | -0.26 | -0.79 | 0.726 | 0.891 | 1.000 | 22334 | tags=47%, list=41%, signal=80% | |
4033 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 64 | -0.23 | -0.79 | 0.748 | 0.891 | 1.000 | 10579 | tags=23%, list=19%, signal=29% | |
4034 | POSITIVE REGULATION OF LYASE ACTIVITY | 90 | -0.21 | -0.79 | 0.791 | 0.891 | 1.000 | 27360 | tags=44%, list=50%, signal=89% | |
4035 | STAT PROTEIN IMPORT INTO NUCLEUS | 13 | -0.28 | -0.79 | 0.732 | 0.891 | 1.000 | 21279 | tags=46%, list=39%, signal=76% | |
4036 | REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE BY CIRCULATORY RENIN-ANGIOTENSIN | 29 | -0.25 | -0.79 | 0.755 | 0.891 | 1.000 | 13274 | tags=28%, list=24%, signal=36% | |
4037 | ATRIOVENTRICULAR VALVE FORMATION | 11 | -0.32 | -0.79 | 0.716 | 0.891 | 1.000 | 5907 | tags=18%, list=11%, signal=20% | |
4038 | INTEGRIN-MEDIATED SIGNALING PATHWAY | 103 | -0.20 | -0.79 | 0.849 | 0.891 | 1.000 | 30177 | tags=54%, list=55%, signal=121% | |
4039 | THIAMINE-CONTAINING COMPOUND METABOLIC PROCESS | 11 | -0.31 | -0.79 | 0.744 | 0.891 | 1.000 | 15699 | tags=36%, list=29%, signal=51% | |
4040 | REGULATION OF MORPHOGENESIS OF A BRANCHING STRUCTURE | 62 | -0.20 | -0.79 | 0.780 | 0.891 | 1.000 | 17093 | tags=31%, list=31%, signal=45% | |
4041 | REGULATION OF DENDRITE EXTENSION | 31 | -0.22 | -0.79 | 0.774 | 0.891 | 1.000 | 24923 | tags=48%, list=46%, signal=89% | |
4042 | POSITIVE REGULATION OF DENDRITE EXTENSION | 31 | -0.22 | -0.79 | 0.774 | 0.890 | 1.000 | 24923 | tags=48%, list=46%, signal=89% | |
4043 | REGULATION OF CELLULAR PH | 78 | -0.22 | -0.79 | 0.764 | 0.890 | 1.000 | 14847 | tags=32%, list=27%, signal=44% | |
4044 | NEGATIVE REGULATION OF INSULIN SECRETION | 28 | -0.24 | -0.79 | 0.782 | 0.891 | 1.000 | 13452 | tags=29%, list=25%, signal=38% | |
4045 | POSITIVE REGULATION OF TOLL-LIKE RECEPTOR 3 SIGNALING PATHWAY | 18 | -0.28 | -0.79 | 0.756 | 0.891 | 1.000 | 19428 | tags=44%, list=36%, signal=69% | |
4046 | VISUAL PERCEPTION | 153 | -0.19 | -0.79 | 0.777 | 0.892 | 1.000 | 22559 | tags=37%, list=41%, signal=63% | |
4047 | RESPONSE TO NERVE GROWTH FACTOR | 39 | -0.25 | -0.79 | 0.764 | 0.892 | 1.000 | 35580 | tags=74%, list=65%, signal=213% | |
4048 | CELLULAR RESPONSE TO NERVE GROWTH FACTOR STIMULUS | 39 | -0.25 | -0.79 | 0.764 | 0.892 | 1.000 | 35580 | tags=74%, list=65%, signal=213% | |
4049 | FACE DEVELOPMENT | 45 | -0.23 | -0.79 | 0.729 | 0.892 | 1.000 | 14720 | tags=29%, list=27%, signal=39% | |
4050 | RETINOIC ACID METABOLIC PROCESS | 13 | -0.30 | -0.79 | 0.728 | 0.892 | 1.000 | 36365 | tags=77%, list=67%, signal=230% | |
4051 | CELLULAR RESPONSE TO ZINC ION | 14 | -0.33 | -0.79 | 0.628 | 0.892 | 1.000 | 28108 | tags=64%, list=51%, signal=132% | |
4052 | PLASMA LIPOPROTEIN PARTICLE ORGANIZATION | 56 | -0.22 | -0.79 | 0.737 | 0.892 | 1.000 | 21720 | tags=39%, list=40%, signal=65% | |
4053 | BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 41 | -0.23 | -0.79 | 0.790 | 0.892 | 1.000 | 29286 | tags=56%, list=54%, signal=121% | |
4054 | VENTRICULAR CARDIAC MUSCLE TISSUE DEVELOPMENT | 61 | -0.20 | -0.79 | 0.799 | 0.894 | 1.000 | 33973 | tags=61%, list=62%, signal=160% | |
4055 | REGULATION OF CARDIAC MUSCLE CONTRACTION | 133 | -0.19 | -0.79 | 0.879 | 0.894 | 1.000 | 26192 | tags=46%, list=48%, signal=88% | |
4056 | REGIONALIZATION | 207 | -0.19 | -0.79 | 0.857 | 0.894 | 1.000 | 34770 | tags=62%, list=64%, signal=171% | |
4057 | REGULATION OF CELLULAR RESPONSE TO OXIDATIVE STRESS | 103 | -0.23 | -0.79 | 0.744 | 0.895 | 1.000 | 19983 | tags=41%, list=37%, signal=64% | |
4058 | STRIATED MUSCLE HYPERTROPHY | 35 | -0.23 | -0.79 | 0.791 | 0.896 | 1.000 | 30729 | tags=60%, list=56%, signal=137% | |
4059 | REGULATION OF INSULIN RECEPTOR SIGNALING PATHWAY | 67 | -0.22 | -0.79 | 0.798 | 0.896 | 1.000 | 29461 | tags=54%, list=54%, signal=116% | |
4060 | PROTEIN HETEROTETRAMERIZATION | 39 | -0.25 | -0.79 | 0.771 | 0.895 | 1.000 | 30141 | tags=62%, list=55%, signal=137% | |
4061 | RESPONSE TO INTERLEUKIN-6 | 51 | -0.23 | -0.79 | 0.780 | 0.896 | 1.000 | 32842 | tags=63%, list=60%, signal=157% | |
4062 | COMMISSURAL NEURON AXON GUIDANCE | 24 | -0.27 | -0.79 | 0.698 | 0.896 | 1.000 | 27706 | tags=54%, list=51%, signal=110% | |
4063 | PROXIMAL/DISTAL PATTERN FORMATION | 10 | -0.29 | -0.79 | 0.735 | 0.896 | 1.000 | 203 | tags=10%, list=0%, signal=10% | |
4064 | LEUKOCYTE DIFFERENTIATION | 305 | -0.19 | -0.79 | 0.853 | 0.897 | 1.000 | 22943 | tags=41%, list=42%, signal=70% | |
4065 | OVULATION CYCLE PROCESS | 45 | -0.23 | -0.79 | 0.783 | 0.896 | 1.000 | 6539 | tags=18%, list=12%, signal=20% | |
4066 | ENDOCHONDRAL BONE GROWTH | 14 | -0.29 | -0.79 | 0.742 | 0.897 | 1.000 | 22529 | tags=43%, list=41%, signal=73% | |
4067 | MYELOID LEUKOCYTE ACTIVATION | 113 | -0.23 | -0.79 | 0.804 | 0.897 | 1.000 | 20765 | tags=41%, list=38%, signal=66% | |
4068 | LEUKOTRIENE CATABOLIC PROCESS | 7 | -0.35 | -0.79 | 0.724 | 0.897 | 1.000 | 28804 | tags=71%, list=53%, signal=151% | |
4069 | LEUKOTRIENE B4 CATABOLIC PROCESS | 7 | -0.35 | -0.79 | 0.724 | 0.897 | 1.000 | 28804 | tags=71%, list=53%, signal=151% | |
4070 | LEUKOTRIENE B4 METABOLIC PROCESS | 7 | -0.35 | -0.79 | 0.724 | 0.897 | 1.000 | 28804 | tags=71%, list=53%, signal=151% | |
4071 | ICOSANOID CATABOLIC PROCESS | 7 | -0.35 | -0.79 | 0.724 | 0.897 | 1.000 | 28804 | tags=71%, list=53%, signal=151% | |
4072 | FATTY ACID DERIVATIVE CATABOLIC PROCESS | 7 | -0.35 | -0.79 | 0.724 | 0.897 | 1.000 | 28804 | tags=71%, list=53%, signal=151% | |
4073 | CHONDROITIN SULFATE PROTEOGLYCAN BIOSYNTHETIC PROCESS | 52 | -0.23 | -0.79 | 0.717 | 0.897 | 1.000 | 27573 | tags=56%, list=50%, signal=112% | |
4074 | POSITIVE REGULATION OF CLATHRIN-MEDIATED ENDOCYTOSIS | 22 | -0.27 | -0.79 | 0.737 | 0.896 | 1.000 | 34956 | tags=73%, list=64%, signal=202% | |
4075 | NEGATIVE REGULATION OF TUMOR NECROSIS FACTOR PRODUCTION | 67 | -0.24 | -0.79 | 0.738 | 0.896 | 1.000 | 4564 | tags=15%, list=8%, signal=16% | |
4076 | SYNAPSIS | 17 | -0.27 | -0.79 | 0.738 | 0.897 | 1.000 | 10382 | tags=24%, list=19%, signal=29% | |
4077 | PH ELEVATION | 19 | -0.28 | -0.79 | 0.737 | 0.897 | 1.000 | 9409 | tags=26%, list=17%, signal=32% | |
4078 | INTRACELLULAR PH ELEVATION | 19 | -0.28 | -0.79 | 0.737 | 0.896 | 1.000 | 9409 | tags=26%, list=17%, signal=32% | |
4079 | NEGATIVE REGULATION OF CELL-MATRIX ADHESION | 79 | -0.22 | -0.79 | 0.739 | 0.896 | 1.000 | 34905 | tags=72%, list=64%, signal=199% | |
4080 | FRUCTOSE METABOLIC PROCESS | 21 | -0.27 | -0.79 | 0.708 | 0.896 | 1.000 | 3499 | tags=19%, list=6%, signal=20% | |
4081 | REGULATION OF RESPONSE TO OXIDATIVE STRESS | 105 | -0.23 | -0.79 | 0.757 | 0.896 | 1.000 | 20519 | tags=42%, list=38%, signal=67% | |
4082 | REGULATION OF MACROPHAGE ACTIVATION | 31 | -0.24 | -0.79 | 0.751 | 0.896 | 1.000 | 34905 | tags=68%, list=64%, signal=187% | |
4083 | REGULATION OF NITRIC OXIDE BIOSYNTHETIC PROCESS | 75 | -0.22 | -0.78 | 0.835 | 0.896 | 1.000 | 14041 | tags=28%, list=26%, signal=38% | |
4084 | NEGATIVE REGULATION OF CELL CYCLE ARREST | 31 | -0.24 | -0.78 | 0.718 | 0.896 | 1.000 | 36296 | tags=71%, list=66%, signal=211% | |
4085 | HEAD DEVELOPMENT | 632 | -0.19 | -0.78 | 0.917 | 0.897 | 1.000 | 31076 | tags=57%, list=57%, signal=130% | |
4086 | CARDIAC CHAMBER MORPHOGENESIS | 145 | -0.19 | -0.78 | 0.822 | 0.897 | 1.000 | 29526 | tags=50%, list=54%, signal=108% | |
4087 | NEGATIVE REGULATION OF T CELL RECEPTOR SIGNALING PATHWAY | 35 | -0.24 | -0.78 | 0.782 | 0.897 | 1.000 | 12958 | tags=29%, list=24%, signal=37% | |
4088 | POSITIVE REGULATION OF REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 72 | -0.22 | -0.78 | 0.842 | 0.897 | 1.000 | 14041 | tags=28%, list=26%, signal=37% | |
4089 | POSITIVE REGULATION OF ACTION POTENTIAL | 18 | -0.26 | -0.78 | 0.714 | 0.897 | 1.000 | 25853 | tags=50%, list=47%, signal=95% | |
4090 | POSITIVE REGULATION OF CELL ADHESION | 639 | -0.19 | -0.78 | 0.848 | 0.897 | 1.000 | 22721 | tags=40%, list=42%, signal=68% | |
4091 | OSSIFICATION INVOLVED IN BONE MATURATION | 15 | -0.28 | -0.78 | 0.728 | 0.897 | 1.000 | 5700 | tags=20%, list=10%, signal=22% | |
4092 | NEGATIVE REGULATION OF SINGLE STRANDED VIRAL RNA REPLICATION VIA DOUBLE STRANDED DNA INTERMEDIATE | 17 | -0.26 | -0.78 | 0.772 | 0.897 | 1.000 | 5883 | tags=24%, list=11%, signal=26% | |
4093 | ACTIN FILAMENT-BASED TRANSPORT | 16 | -0.28 | -0.78 | 0.744 | 0.897 | 1.000 | 27825 | tags=50%, list=51%, signal=102% | |
4094 | ENDOPLASMIC RETICULUM TUBULAR NETWORK ORGANIZATION | 17 | -0.30 | -0.78 | 0.739 | 0.897 | 1.000 | 26511 | tags=65%, list=48%, signal=126% | |
4095 | CELL COMMUNICATION INVOLVED IN CARDIAC CONDUCTION | 79 | -0.20 | -0.78 | 0.817 | 0.897 | 1.000 | 22927 | tags=39%, list=42%, signal=67% | |
4096 | CORONARY VASCULATURE DEVELOPMENT | 21 | -0.26 | -0.78 | 0.718 | 0.897 | 1.000 | 29526 | tags=52%, list=54%, signal=114% | |
4097 | KERATINOCYTE PROLIFERATION | 14 | -0.29 | -0.78 | 0.744 | 0.897 | 1.000 | 19569 | tags=43%, list=36%, signal=67% | |
4098 | SENSORY PERCEPTION OF LIGHT STIMULUS | 174 | -0.18 | -0.78 | 0.805 | 0.899 | 1.000 | 24390 | tags=40%, list=45%, signal=71% | |
4099 | REGULATION OF DOPAMINE RECEPTOR SIGNALING PATHWAY | 17 | -0.28 | -0.78 | 0.704 | 0.899 | 1.000 | 14479 | tags=35%, list=26%, signal=48% | |
4100 | CELLULAR RESPONSE TO METAL ION | 164 | -0.19 | -0.78 | 0.842 | 0.899 | 1.000 | 29286 | tags=54%, list=54%, signal=115% | |
4101 | STRESS-INDUCED PREMATURE SENESCENCE | 17 | -0.29 | -0.78 | 0.728 | 0.899 | 1.000 | 14017 | tags=35%, list=26%, signal=47% | |
4102 | CEREBRAL CORTEX DEVELOPMENT | 102 | -0.22 | -0.78 | 0.750 | 0.899 | 1.000 | 24273 | tags=47%, list=44%, signal=84% | |
4103 | POSITIVE REGULATION OF EPITHELIAL CELL PROLIFERATION INVOLVED IN WOUND HEALING | 6 | -0.34 | -0.78 | 0.771 | 0.899 | 1.000 | 31368 | tags=83%, list=57%, signal=195% | |
4104 | HISTONE PHOSPHORYLATION | 69 | -0.21 | -0.78 | 0.806 | 0.899 | 1.000 | 15652 | tags=32%, list=29%, signal=45% | |
4105 | BRAIN DEVELOPMENT | 598 | -0.19 | -0.78 | 0.917 | 0.899 | 1.000 | 31550 | tags=58%, list=58%, signal=135% | |
4106 | NEGATIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT PROTEIN | 22 | -0.25 | -0.78 | 0.749 | 0.900 | 1.000 | 35692 | tags=82%, list=65%, signal=236% | |
4107 | REGULATION OF NATURAL KILLER CELL ACTIVATION | 26 | -0.26 | -0.78 | 0.749 | 0.900 | 1.000 | 34452 | tags=77%, list=63%, signal=208% | |
4108 | EMBRYONIC SKELETAL JOINT DEVELOPMENT | 10 | -0.30 | -0.78 | 0.757 | 0.899 | 1.000 | 30361 | tags=60%, list=56%, signal=135% | |
4109 | NATURAL KILLER CELL MEDIATED CYTOTOXICITY | 20 | -0.27 | -0.78 | 0.781 | 0.899 | 1.000 | 35336 | tags=80%, list=65%, signal=226% | |
4110 | AUTONOMIC NERVOUS SYSTEM DEVELOPMENT | 77 | -0.21 | -0.78 | 0.832 | 0.899 | 1.000 | 35937 | tags=70%, list=66%, signal=204% | |
4111 | DENDRITIC SPINE ORGANIZATION | 36 | -0.22 | -0.78 | 0.785 | 0.899 | 1.000 | 29821 | tags=61%, list=55%, signal=134% | |
4112 | REGULATION OF HORMONE LEVELS | 689 | -0.18 | -0.78 | 0.843 | 0.899 | 1.000 | 23143 | tags=39%, list=42%, signal=67% | |
4113 | NEGATIVE REGULATION OF FAT CELL DIFFERENTIATION | 65 | -0.21 | -0.78 | 0.792 | 0.899 | 1.000 | 23158 | tags=42%, list=42%, signal=72% | |
4114 | REGULATION OF CHEMOKINE SECRETION | 11 | -0.31 | -0.78 | 0.741 | 0.899 | 1.000 | 37034 | tags=91%, list=68%, signal=282% | |
4115 | REGULATION OF MYOBLAST DIFFERENTIATION | 58 | -0.20 | -0.78 | 0.791 | 0.899 | 1.000 | 7135 | tags=17%, list=13%, signal=20% | |
4116 | LYMPHOCYTE ACTIVATION INVOLVED IN IMMUNE RESPONSE | 108 | -0.21 | -0.78 | 0.811 | 0.899 | 1.000 | 17837 | tags=35%, list=33%, signal=52% | |
4117 | LYMPHOCYTE DIFFERENTIATION | 210 | -0.19 | -0.78 | 0.883 | 0.899 | 1.000 | 31392 | tags=57%, list=57%, signal=133% | |
4118 | INTRACILIARY TRANSPORT | 38 | -0.29 | -0.78 | 0.652 | 0.899 | 1.000 | 35980 | tags=89%, list=66%, signal=261% | |
4119 | PROTEIN TRANSPORT ALONG MICROTUBULE | 38 | -0.29 | -0.78 | 0.652 | 0.899 | 1.000 | 35980 | tags=89%, list=66%, signal=261% | |
4120 | CELLULAR RESPONSE TO CAMP | 70 | -0.21 | -0.78 | 0.812 | 0.899 | 1.000 | 16270 | tags=30%, list=30%, signal=43% | |
4121 | RECEPTOR GUANYLYL CYCLASE SIGNALING PATHWAY | 12 | -0.31 | -0.78 | 0.736 | 0.899 | 1.000 | 6106 | tags=17%, list=11%, signal=19% | |
4122 | SINGLE FERTILIZATION | 85 | -0.21 | -0.78 | 0.832 | 0.899 | 1.000 | 21572 | tags=38%, list=39%, signal=62% | |
4123 | DNA GEOMETRIC CHANGE | 131 | -0.22 | -0.78 | 0.751 | 0.899 | 1.000 | 35005 | tags=71%, list=64%, signal=197% | |
4124 | GLYCOSPHINGOLIPID CATABOLIC PROCESS | 11 | -0.30 | -0.78 | 0.738 | 0.899 | 1.000 | 25665 | tags=55%, list=47%, signal=103% | |
4125 | POSITIVE REGULATION OF ANION TRANSPORT | 54 | -0.22 | -0.78 | 0.830 | 0.899 | 1.000 | 14887 | tags=31%, list=27%, signal=43% | |
4126 | POSITIVE REGULATION OF MACROPHAGE ACTIVATION | 23 | -0.27 | -0.78 | 0.714 | 0.899 | 1.000 | 5047 | tags=17%, list=9%, signal=19% | |
4127 | MONOCYTE CHEMOTAXIS | 29 | -0.26 | -0.78 | 0.735 | 0.899 | 1.000 | 22408 | tags=41%, list=41%, signal=70% | |
4128 | POSITIVE REGULATION OF CYCLASE ACTIVITY | 97 | -0.20 | -0.78 | 0.838 | 0.900 | 1.000 | 27360 | tags=44%, list=50%, signal=89% | |
4129 | REGULATION OF TRANSPOSITION | 16 | -0.27 | -0.78 | 0.740 | 0.900 | 1.000 | 2356 | tags=19%, list=4%, signal=20% | |
4130 | NEGATIVE REGULATION OF TRANSPOSITION | 16 | -0.27 | -0.78 | 0.740 | 0.899 | 1.000 | 2356 | tags=19%, list=4%, signal=20% | |
4131 | EMBRYONIC MORPHOGENESIS | 512 | -0.18 | -0.78 | 0.894 | 0.899 | 1.000 | 31192 | tags=54%, list=57%, signal=124% | |
4132 | AMP METABOLIC PROCESS | 18 | -0.28 | -0.78 | 0.734 | 0.899 | 1.000 | 19834 | tags=50%, list=36%, signal=78% | |
4133 | SERTOLI CELL DIFFERENTIATION | 7 | -0.33 | -0.78 | 0.738 | 0.900 | 1.000 | 6904 | tags=29%, list=13%, signal=33% | |
4134 | TONGUE DEVELOPMENT | 12 | -0.28 | -0.78 | 0.736 | 0.900 | 1.000 | 12604 | tags=33%, list=23%, signal=43% | |
4135 | NEGATIVE REGULATION OF CELL-SUBSTRATE ADHESION | 126 | -0.20 | -0.78 | 0.798 | 0.900 | 1.000 | 36972 | tags=72%, list=68%, signal=223% | |
4136 | CELLULAR RESPONSE TO INORGANIC SUBSTANCE | 184 | -0.19 | -0.78 | 0.863 | 0.900 | 1.000 | 29286 | tags=53%, list=54%, signal=114% | |
4137 | REGULATION OF RELEASE OF SEQUESTERED CALCIUM ION INTO CYTOSOL BY SARCOPLASMIC RETICULUM | 73 | -0.21 | -0.78 | 0.804 | 0.900 | 1.000 | 28323 | tags=52%, list=52%, signal=108% | |
4138 | POSITIVE REGULATION OF METALLOENZYME ACTIVITY | 11 | -0.30 | -0.78 | 0.722 | 0.900 | 1.000 | 15238 | tags=36%, list=28%, signal=50% | |
4139 | RESPONSE TO INORGANIC SUBSTANCE | 424 | -0.19 | -0.78 | 0.898 | 0.900 | 1.000 | 22040 | tags=39%, list=40%, signal=65% | |
4140 | REGULATION OF RESPONSE TO REACTIVE OXYGEN SPECIES | 55 | -0.23 | -0.78 | 0.794 | 0.900 | 1.000 | 9001 | tags=22%, list=16%, signal=26% | |
4141 | POSITIVE REGULATION OF CELLULAR AMINE METABOLIC PROCESS | 26 | -0.25 | -0.78 | 0.726 | 0.900 | 1.000 | 24948 | tags=50%, list=46%, signal=92% | |
4142 | REGULATION OF NEURON MIGRATION | 31 | -0.24 | -0.78 | 0.731 | 0.900 | 1.000 | 12581 | tags=29%, list=23%, signal=38% | |
4143 | REGULATION OF KERATINOCYTE PROLIFERATION | 41 | -0.23 | -0.78 | 0.794 | 0.900 | 1.000 | 21643 | tags=44%, list=40%, signal=73% | |
4144 | VITAMIN TRANSMEMBRANE TRANSPORT | 13 | -0.29 | -0.78 | 0.738 | 0.900 | 1.000 | 953 | tags=15%, list=2%, signal=16% | |
4145 | RESPONSE TO AXON INJURY | 16 | -0.29 | -0.78 | 0.743 | 0.900 | 1.000 | 37370 | tags=94%, list=68%, signal=296% | |
4146 | POSTTRANSLATIONAL PROTEIN TARGETING TO MEMBRANE | 16 | -0.33 | -0.78 | 0.709 | 0.900 | 1.000 | 30603 | tags=81%, list=56%, signal=184% | |
4147 | CELLULAR ANION HOMEOSTASIS | 15 | -0.28 | -0.78 | 0.774 | 0.900 | 1.000 | 35541 | tags=80%, list=65%, signal=229% | |
4148 | CELLULAR MONOVALENT INORGANIC ANION HOMEOSTASIS | 15 | -0.28 | -0.78 | 0.774 | 0.899 | 1.000 | 35541 | tags=80%, list=65%, signal=229% | |
4149 | PROTEIN HETEROOLIGOMERIZATION | 109 | -0.21 | -0.78 | 0.770 | 0.900 | 1.000 | 14137 | tags=28%, list=26%, signal=38% | |
4150 | POSITIVE REGULATION OF PHOSPHOLIPID BIOSYNTHETIC PROCESS | 12 | -0.30 | -0.78 | 0.717 | 0.901 | 1.000 | 31126 | tags=75%, list=57%, signal=174% | |
4151 | PURINE RIBONUCLEOTIDE CATABOLIC PROCESS | 51 | -0.22 | -0.77 | 0.830 | 0.901 | 1.000 | 29333 | tags=51%, list=54%, signal=110% | |
4152 | TERPENOID METABOLIC PROCESS | 167 | -0.19 | -0.77 | 0.828 | 0.901 | 1.000 | 33967 | tags=60%, list=62%, signal=159% | |
4153 | CELLULAR RESPONSE TO NITRIC OXIDE | 17 | -0.26 | -0.77 | 0.763 | 0.901 | 1.000 | 26785 | tags=53%, list=49%, signal=104% | |
4154 | CELLULAR RESPONSE TO REACTIVE NITROGEN SPECIES | 17 | -0.26 | -0.77 | 0.763 | 0.900 | 1.000 | 26785 | tags=53%, list=49%, signal=104% | |
4155 | ACTIN FILAMENT SEVERING | 21 | -0.27 | -0.77 | 0.771 | 0.901 | 1.000 | 14978 | tags=38%, list=27%, signal=52% | |
4156 | RESPONSE TO BACTERIUM | 482 | -0.20 | -0.77 | 0.774 | 0.901 | 1.000 | 25181 | tags=45%, list=46%, signal=83% | |
4157 | PALLIUM DEVELOPMENT | 130 | -0.21 | -0.77 | 0.806 | 0.901 | 1.000 | 31550 | tags=62%, list=58%, signal=145% | |
4158 | REGULATION OF RECEPTOR ACTIVITY | 281 | -0.18 | -0.77 | 0.911 | 0.902 | 1.000 | 19954 | tags=34%, list=36%, signal=53% | |
4159 | REGULATION OF VENTRICULAR CARDIAC MUSCLE CELL ACTION POTENTIAL | 25 | -0.25 | -0.77 | 0.765 | 0.902 | 1.000 | 31662 | tags=60%, list=58%, signal=142% | |
4160 | POSITIVE REGULATION OF LYMPHOCYTE DIFFERENTIATION | 89 | -0.21 | -0.77 | 0.794 | 0.902 | 1.000 | 17788 | tags=31%, list=33%, signal=47% | |
4161 | METANEPHRIC NEPHRON EPITHELIUM DEVELOPMENT | 25 | -0.25 | -0.77 | 0.744 | 0.901 | 1.000 | 17093 | tags=32%, list=31%, signal=47% | |
4162 | CERAMIDE METABOLIC PROCESS | 78 | -0.21 | -0.77 | 0.812 | 0.901 | 1.000 | 18662 | tags=36%, list=34%, signal=54% | |
4163 | NEGATIVE REGULATION OF CD4-POSITIVE, ALPHA-BETA T CELL DIFFERENTIATION | 21 | -0.25 | -0.77 | 0.716 | 0.901 | 1.000 | 30991 | tags=62%, list=57%, signal=143% | |
4164 | CARDIAC MUSCLE TISSUE GROWTH | 30 | -0.24 | -0.77 | 0.751 | 0.903 | 1.000 | 26563 | tags=53%, list=49%, signal=104% | |
4165 | CELLULAR RESPONSE TO BIOTIC STIMULUS | 188 | -0.23 | -0.77 | 0.773 | 0.904 | 1.000 | 25005 | tags=46%, list=46%, signal=85% | |
4166 | NEGATIVE REGULATION OF MACROPHAGE DIFFERENTIATION | 12 | -0.30 | -0.77 | 0.751 | 0.904 | 1.000 | 34080 | tags=83%, list=62%, signal=221% | |
4167 | REGULATION OF B CELL ACTIVATION | 133 | -0.21 | -0.77 | 0.773 | 0.905 | 1.000 | 5072 | tags=15%, list=9%, signal=17% | |
4168 | RESPONSE TO PURINE-CONTAINING COMPOUND | 135 | -0.19 | -0.77 | 0.870 | 0.906 | 1.000 | 16270 | tags=28%, list=30%, signal=40% | |
4169 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT1 PROTEIN | 21 | -0.27 | -0.77 | 0.759 | 0.906 | 1.000 | 17302 | tags=38%, list=32%, signal=56% | |
4170 | NITROGEN CYCLE METABOLIC PROCESS | 23 | -0.25 | -0.77 | 0.770 | 0.906 | 1.000 | 33749 | tags=70%, list=62%, signal=182% | |
4171 | POSITIVE REGULATION OF DNA-TEMPLATED TRANSCRIPTION, INITIATION | 29 | -0.25 | -0.77 | 0.775 | 0.906 | 1.000 | 34438 | tags=76%, list=63%, signal=205% | |
4172 | CARDIAC RIGHT VENTRICLE MORPHOGENESIS | 26 | -0.25 | -0.77 | 0.810 | 0.907 | 1.000 | 12962 | tags=31%, list=24%, signal=40% | |
4173 | AMINO SUGAR BIOSYNTHETIC PROCESS | 10 | -0.35 | -0.77 | 0.736 | 0.907 | 1.000 | 32265 | tags=90%, list=59%, signal=220% | |
4174 | REGULATION OF PROTEIN AUTOPHOSPHORYLATION | 70 | -0.21 | -0.77 | 0.805 | 0.907 | 1.000 | 22100 | tags=44%, list=40%, signal=74% | |
4175 | REGULATION OF ADENYLATE CYCLASE ACTIVITY | 108 | -0.20 | -0.77 | 0.827 | 0.907 | 1.000 | 28908 | tags=46%, list=53%, signal=98% | |
4176 | NEUTROPHIL CHEMOTAXIS | 46 | -0.28 | -0.77 | 0.748 | 0.907 | 1.000 | 17066 | tags=35%, list=31%, signal=51% | |
4177 | REGULATION OF ANION TRANSPORT | 175 | -0.19 | -0.77 | 0.877 | 0.907 | 1.000 | 19742 | tags=36%, list=36%, signal=56% | |
4178 | REGULATION OF MITOCHONDRIAL MEMBRANE PERMEABILITY INVOLVED IN APOPTOTIC PROCESS | 22 | -0.24 | -0.77 | 0.721 | 0.907 | 1.000 | 7559 | tags=23%, list=14%, signal=26% | |
4179 | DNA DUPLEX UNWINDING | 119 | -0.22 | -0.77 | 0.756 | 0.907 | 1.000 | 35005 | tags=71%, list=64%, signal=196% | |
4180 | DEVELOPMENTAL PROCESS INVOLVED IN REPRODUCTION | 368 | -0.17 | -0.77 | 0.918 | 0.907 | 1.000 | 24309 | tags=40%, list=44%, signal=72% | |
4181 | REGULATION OF EPITHELIAL CELL MIGRATION | 404 | -0.18 | -0.77 | 0.901 | 0.907 | 1.000 | 36113 | tags=67%, list=66%, signal=195% | |
4182 | POSITIVE REGULATION OF LEUKOCYTE APOPTOTIC PROCESS | 36 | -0.24 | -0.77 | 0.784 | 0.907 | 1.000 | 30021 | tags=64%, list=55%, signal=142% | |
4183 | NEGATIVE REGULATION OF MUSCLE ORGAN DEVELOPMENT | 37 | -0.22 | -0.77 | 0.772 | 0.907 | 1.000 | 25734 | tags=46%, list=47%, signal=87% | |
4184 | MITOTIC CELL CYCLE ARREST | 25 | -0.25 | -0.77 | 0.747 | 0.907 | 1.000 | 35787 | tags=72%, list=65%, signal=208% | |
4185 | POSITIVE REGULATION OF GLYCOLYTIC PROCESS | 27 | -0.25 | -0.77 | 0.768 | 0.907 | 1.000 | 24473 | tags=52%, list=45%, signal=94% | |
4186 | CELLULAR TRIGLYCERIDE HOMEOSTASIS | 16 | -0.27 | -0.77 | 0.797 | 0.907 | 1.000 | 26193 | tags=56%, list=48%, signal=108% | |
4187 | ASTROCYTE DIFFERENTIATION | 27 | -0.25 | -0.77 | 0.722 | 0.907 | 1.000 | 30781 | tags=70%, list=56%, signal=161% | |
4188 | POSITIVE REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS BY VEGF-ACTIVATED VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 11 | -0.30 | -0.77 | 0.772 | 0.907 | 1.000 | 1411 | tags=18%, list=3%, signal=19% | |
4189 | PROTEIN KINASE B SIGNALING | 48 | -0.26 | -0.77 | 0.754 | 0.907 | 1.000 | 18711 | tags=42%, list=34%, signal=63% | |
4190 | RIBONUCLEOTIDE CATABOLIC PROCESS | 54 | -0.22 | -0.77 | 0.831 | 0.907 | 1.000 | 28323 | tags=50%, list=52%, signal=104% | |
4191 | NEGATIVE REGULATION OF CHROMATIN SILENCING | 11 | -0.31 | -0.77 | 0.739 | 0.907 | 1.000 | 2994 | tags=18%, list=5%, signal=19% | |
4192 | RESPONSE TO MECHANICAL STIMULUS | 176 | -0.20 | -0.77 | 0.870 | 0.907 | 1.000 | 23678 | tags=43%, list=43%, signal=76% | |
4193 | REGULATION OF LEUKOCYTE CELL-CELL ADHESION | 484 | -0.19 | -0.77 | 0.846 | 0.907 | 1.000 | 23916 | tags=42%, list=44%, signal=75% | |
4194 | NITRIC OXIDE MEDIATED SIGNAL TRANSDUCTION | 31 | -0.24 | -0.77 | 0.798 | 0.907 | 1.000 | 25780 | tags=48%, list=47%, signal=92% | |
4195 | MEIOTIC CHROMOSOME SEGREGATION | 35 | -0.21 | -0.77 | 0.798 | 0.907 | 1.000 | 5264 | tags=14%, list=10%, signal=16% | |
4196 | SYMPATHETIC NERVOUS SYSTEM DEVELOPMENT | 61 | -0.21 | -0.77 | 0.794 | 0.907 | 1.000 | 35937 | tags=72%, list=66%, signal=210% | |
4197 | REGULATION OF LIPID BIOSYNTHETIC PROCESS | 195 | -0.18 | -0.77 | 0.908 | 0.907 | 1.000 | 16692 | tags=30%, list=31%, signal=43% | |
4198 | I-KAPPAB PHOSPHORYLATION | 27 | -0.26 | -0.77 | 0.791 | 0.907 | 1.000 | 15474 | tags=37%, list=28%, signal=52% | |
4199 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE PHOSPHATASE SIGNALING PATHWAY | 24 | -0.25 | -0.77 | 0.770 | 0.907 | 1.000 | 37918 | tags=88%, list=69%, signal=285% | |
4200 | DIGESTIVE TRACT MORPHOGENESIS | 54 | -0.21 | -0.77 | 0.810 | 0.907 | 1.000 | 30616 | tags=56%, list=56%, signal=126% | |
4201 | POSITIVE REGULATION OF ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 120 | -0.18 | -0.77 | 0.897 | 0.907 | 1.000 | 26595 | tags=48%, list=49%, signal=94% | |
4202 | REGULATION OF CHROMATIN ASSEMBLY OR DISASSEMBLY | 31 | -0.23 | -0.77 | 0.808 | 0.907 | 1.000 | 31967 | tags=61%, list=58%, signal=147% | |
4203 | NEGATIVE REGULATION OF DNA DAMAGE RESPONSE, SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 38 | -0.24 | -0.77 | 0.750 | 0.907 | 1.000 | 21540 | tags=47%, list=39%, signal=78% | |
4204 | RESPONSE TO DRUG | 263 | -0.18 | -0.77 | 0.888 | 0.908 | 1.000 | 32064 | tags=58%, list=59%, signal=140% | |
4205 | POSITIVE REGULATION OF EARLY ENDOSOME TO LATE ENDOSOME TRANSPORT | 26 | -0.27 | -0.76 | 0.731 | 0.908 | 1.000 | 34794 | tags=77%, list=64%, signal=211% | |
4206 | POSITIVE REGULATION OF TRANSLATIONAL INITIATION | 44 | -0.25 | -0.76 | 0.766 | 0.908 | 1.000 | 38819 | tags=86%, list=71%, signal=298% | |
4207 | AXONEMAL DYNEIN COMPLEX ASSEMBLY | 45 | -0.26 | -0.76 | 0.683 | 0.908 | 1.000 | 34039 | tags=76%, list=62%, signal=200% | |
4208 | EXTRACELLULAR REGULATION OF SIGNAL TRANSDUCTION | 34 | -0.23 | -0.76 | 0.812 | 0.908 | 1.000 | 6046 | tags=18%, list=11%, signal=20% | |
4209 | EXTRACELLULAR NEGATIVE REGULATION OF SIGNAL TRANSDUCTION | 34 | -0.23 | -0.76 | 0.812 | 0.907 | 1.000 | 6046 | tags=18%, list=11%, signal=20% | |
4210 | HEART DEVELOPMENT | 531 | -0.17 | -0.76 | 0.956 | 0.907 | 1.000 | 32216 | tags=56%, list=59%, signal=134% | |
4211 | POSITIVE REGULATION OF SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 40 | -0.23 | -0.76 | 0.779 | 0.908 | 1.000 | 34726 | tags=70%, list=64%, signal=192% | |
4212 | CARDIAC MUSCLE HYPERTROPHY | 34 | -0.22 | -0.76 | 0.810 | 0.908 | 1.000 | 32126 | tags=62%, list=59%, signal=150% | |
4213 | CERAMIDE CATABOLIC PROCESS | 12 | -0.29 | -0.76 | 0.766 | 0.908 | 1.000 | 25665 | tags=50%, list=47%, signal=94% | |
4214 | REPRODUCTIVE STRUCTURE DEVELOPMENT | 226 | -0.18 | -0.76 | 0.898 | 0.908 | 1.000 | 33443 | tags=59%, list=61%, signal=151% | |
4215 | REPRODUCTIVE SYSTEM DEVELOPMENT | 226 | -0.18 | -0.76 | 0.898 | 0.908 | 1.000 | 33443 | tags=59%, list=61%, signal=151% | |
4216 | REGULATION OF MYOBLAST FUSION | 34 | -0.30 | -0.76 | 0.750 | 0.908 | 1.000 | 18530 | tags=44%, list=34%, signal=67% | |
4217 | UDP-N-ACETYLGLUCOSAMINE METABOLIC PROCESS | 12 | -0.33 | -0.76 | 0.713 | 0.908 | 1.000 | 36662 | tags=100%, list=67%, signal=303% | |
4218 | POSITIVE REGULATION OF ORGANIC ACID TRANSPORT | 21 | -0.27 | -0.76 | 0.787 | 0.908 | 1.000 | 33046 | tags=71%, list=60%, signal=180% | |
4219 | REGULATION OF HOMOTYPIC CELL-CELL ADHESION | 495 | -0.19 | -0.76 | 0.838 | 0.909 | 1.000 | 23916 | tags=42%, list=44%, signal=73% | |
4220 | VENTRICULAR CARDIAC MUSCLE CELL DIFFERENTIATION | 20 | -0.25 | -0.76 | 0.843 | 0.909 | 1.000 | 33704 | tags=70%, list=62%, signal=182% | |
4221 | RESPONSE TO FLUID SHEAR STRESS | 47 | -0.22 | -0.76 | 0.804 | 0.909 | 1.000 | 24370 | tags=45%, list=45%, signal=81% | |
4222 | AMIDE TRANSPORT | 107 | -0.19 | -0.76 | 0.867 | 0.908 | 1.000 | 26322 | tags=44%, list=48%, signal=85% | |
4223 | VENTRICULAR CARDIAC MUSCLE CELL ACTION POTENTIAL | 25 | -0.23 | -0.76 | 0.786 | 0.908 | 1.000 | 25209 | tags=44%, list=46%, signal=82% | |
4224 | LONG-CHAIN FATTY ACID IMPORT | 15 | -0.29 | -0.76 | 0.715 | 0.908 | 1.000 | 30294 | tags=73%, list=55%, signal=164% | |
4225 | NEGATIVE REGULATION OF HEMATOPOIETIC PROGENITOR CELL DIFFERENTIATION | 30 | -0.23 | -0.76 | 0.826 | 0.908 | 1.000 | 28239 | tags=57%, list=52%, signal=117% | |
4226 | CENTRAL NERVOUS SYSTEM DEVELOPMENT | 813 | -0.18 | -0.76 | 0.947 | 0.908 | 1.000 | 31550 | tags=56%, list=58%, signal=131% | |
4227 | CORONARY VASCULATURE MORPHOGENESIS | 16 | -0.28 | -0.76 | 0.742 | 0.908 | 1.000 | 15405 | tags=31%, list=28%, signal=43% | |
4228 | REGULATION OF WNT SIGNALING PATHWAY, PLANAR CELL POLARITY PATHWAY | 19 | -0.26 | -0.76 | 0.756 | 0.908 | 1.000 | 35979 | tags=84%, list=66%, signal=246% | |
4229 | SERINE FAMILY AMINO ACID CATABOLIC PROCESS | 18 | -0.25 | -0.76 | 0.775 | 0.909 | 1.000 | 17026 | tags=33%, list=31%, signal=48% | |
4230 | CEREBELLAR CORTEX MORPHOGENESIS | 27 | -0.23 | -0.76 | 0.783 | 0.909 | 1.000 | 33770 | tags=67%, list=62%, signal=174% | |
4231 | REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 188 | -0.19 | -0.76 | 0.851 | 0.909 | 1.000 | 35838 | tags=68%, list=66%, signal=195% | |
4232 | NEGATIVE REGULATION OF PEPTIDE HORMONE SECRETION | 29 | -0.23 | -0.76 | 0.811 | 0.909 | 1.000 | 13452 | tags=28%, list=25%, signal=37% | |
4233 | REGULATION OF FAT CELL DIFFERENTIATION | 142 | -0.19 | -0.76 | 0.891 | 0.910 | 1.000 | 23561 | tags=42%, list=43%, signal=73% | |
4234 | HORMONE BIOSYNTHETIC PROCESS | 58 | -0.20 | -0.76 | 0.845 | 0.910 | 1.000 | 23788 | tags=41%, list=44%, signal=73% | |
4235 | GABAERGIC NEURON DIFFERENTIATION | 14 | -0.29 | -0.76 | 0.788 | 0.910 | 1.000 | 36712 | tags=86%, list=67%, signal=261% | |
4236 | PROTEIN UFMYLATION | 12 | -0.31 | -0.76 | 0.736 | 0.910 | 1.000 | 27635 | tags=67%, list=51%, signal=135% | |
4237 | REPLICATION FORK PROCESSING | 42 | -0.22 | -0.76 | 0.838 | 0.910 | 1.000 | 33781 | tags=62%, list=62%, signal=162% | |
4238 | NEGATIVE REGULATION OF IMMUNE RESPONSE | 178 | -0.21 | -0.76 | 0.795 | 0.910 | 1.000 | 14348 | tags=29%, list=26%, signal=39% | |
4239 | POSITIVE REGULATION OF STEM CELL PROLIFERATION | 91 | -0.20 | -0.76 | 0.867 | 0.911 | 1.000 | 15718 | tags=30%, list=29%, signal=42% | |
4240 | ANGIOGENESIS INVOLVED IN WOUND HEALING | 17 | -0.27 | -0.76 | 0.752 | 0.911 | 1.000 | 37449 | tags=88%, list=68%, signal=280% | |
4241 | POSITIVE REGULATION OF MYOBLAST DIFFERENTIATION | 31 | -0.21 | -0.76 | 0.803 | 0.910 | 1.000 | 35905 | tags=68%, list=66%, signal=197% | |
4242 | REGULATION OF CELL FATE COMMITMENT | 29 | -0.23 | -0.76 | 0.764 | 0.910 | 1.000 | 31642 | tags=59%, list=58%, signal=139% | |
4243 | NEURON MIGRATION | 90 | -0.20 | -0.76 | 0.858 | 0.910 | 1.000 | 36829 | tags=70%, list=67%, signal=214% | |
4244 | POSITIVE REGULATION OF MITOCHONDRIAL MEMBRANE PERMEABILITY | 14 | -0.29 | -0.76 | 0.704 | 0.910 | 1.000 | 26545 | tags=64%, list=49%, signal=125% | |
4245 | SKELETAL SYSTEM DEVELOPMENT | 508 | -0.17 | -0.76 | 0.894 | 0.910 | 1.000 | 30361 | tags=50%, list=56%, signal=111% | |
4246 | DITERPENOID METABOLIC PROCESS | 145 | -0.18 | -0.76 | 0.843 | 0.911 | 1.000 | 33967 | tags=60%, list=62%, signal=158% | |
4247 | HYPEROSMOTIC RESPONSE | 13 | -0.27 | -0.76 | 0.773 | 0.911 | 1.000 | 29518 | tags=62%, list=54%, signal=134% | |
4248 | CELLULAR HYPEROSMOTIC RESPONSE | 13 | -0.27 | -0.76 | 0.773 | 0.911 | 1.000 | 29518 | tags=62%, list=54%, signal=134% | |
4249 | RETINA DEVELOPMENT IN CAMERA-TYPE EYE | 116 | -0.18 | -0.76 | 0.860 | 0.911 | 1.000 | 7620 | tags=17%, list=14%, signal=20% | |
4250 | REGULATION OF STEROID METABOLIC PROCESS | 101 | -0.20 | -0.76 | 0.858 | 0.911 | 1.000 | 16531 | tags=31%, list=30%, signal=44% | |
4251 | EPOXYGENASE P450 PATHWAY | 26 | -0.26 | -0.76 | 0.723 | 0.911 | 1.000 | 33525 | tags=77%, list=61%, signal=199% | |
4252 | IMMATURE B CELL DIFFERENTIATION | 18 | -0.27 | -0.76 | 0.744 | 0.911 | 1.000 | 29422 | tags=61%, list=54%, signal=132% | |
4253 | AGING | 153 | -0.19 | -0.76 | 0.896 | 0.911 | 1.000 | 24508 | tags=42%, list=45%, signal=77% | |
4254 | REGULATION OF INTERLEUKIN-23 PRODUCTION | 18 | -0.33 | -0.76 | 0.745 | 0.912 | 1.000 | 18525 | tags=44%, list=34%, signal=67% | |
4255 | REGULATION OF KERATINOCYTE MIGRATION | 15 | -0.27 | -0.76 | 0.814 | 0.912 | 1.000 | 35255 | tags=80%, list=64%, signal=225% | |
4256 | POSITIVE REGULATION OF KERATINOCYTE MIGRATION | 15 | -0.27 | -0.76 | 0.814 | 0.911 | 1.000 | 35255 | tags=80%, list=64%, signal=225% | |
4257 | HISTONE-THREONINE PHOSPHORYLATION | 23 | -0.26 | -0.76 | 0.801 | 0.911 | 1.000 | 18140 | tags=39%, list=33%, signal=59% | |
4258 | LUNG EPITHELIUM DEVELOPMENT | 20 | -0.26 | -0.76 | 0.807 | 0.912 | 1.000 | 16370 | tags=35%, list=30%, signal=50% | |
4259 | DETECTION OF BIOTIC STIMULUS | 46 | -0.26 | -0.76 | 0.776 | 0.912 | 1.000 | 22804 | tags=46%, list=42%, signal=78% | |
4260 | POSITIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 219 | -0.18 | -0.76 | 0.899 | 0.912 | 1.000 | 35937 | tags=64%, list=66%, signal=186% | |
4261 | VITAMIN BIOSYNTHETIC PROCESS | 9 | -0.31 | -0.76 | 0.770 | 0.913 | 1.000 | 6100 | tags=22%, list=11%, signal=25% | |
4262 | FAT-SOLUBLE VITAMIN BIOSYNTHETIC PROCESS | 9 | -0.31 | -0.76 | 0.770 | 0.913 | 1.000 | 6100 | tags=22%, list=11%, signal=25% | |
4263 | CELL SURFACE RECEPTOR SIGNALING PATHWAY INVOLVED IN HEART DEVELOPMENT | 18 | -0.25 | -0.76 | 0.793 | 0.913 | 1.000 | 23703 | tags=44%, list=43%, signal=78% | |
4264 | REGULATION OF T CELL TOLERANCE INDUCTION | 17 | -0.28 | -0.75 | 0.722 | 0.914 | 1.000 | 26021 | tags=59%, list=48%, signal=112% | |
4265 | CD4-POSITIVE, ALPHA-BETA T CELL ACTIVATION | 50 | -0.22 | -0.75 | 0.794 | 0.914 | 1.000 | 31167 | tags=60%, list=57%, signal=139% | |
4266 | INTERLEUKIN-8 PRODUCTION | 12 | -0.29 | -0.75 | 0.801 | 0.914 | 1.000 | 25314 | tags=58%, list=46%, signal=109% | |
4267 | REGULATION OF CD4-POSITIVE, ALPHA-BETA T CELL ACTIVATION | 55 | -0.23 | -0.75 | 0.750 | 0.915 | 1.000 | 28398 | tags=49%, list=52%, signal=102% | |
4268 | CELLULAR DIVALENT INORGANIC ANION HOMEOSTASIS | 14 | -0.27 | -0.75 | 0.806 | 0.915 | 1.000 | 35541 | tags=79%, list=65%, signal=224% | |
4269 | FOREBRAIN DEVELOPMENT | 287 | -0.19 | -0.75 | 0.916 | 0.915 | 1.000 | 36790 | tags=71%, list=67%, signal=216% | |
4270 | REGULATION OF T CELL ACTIVATION | 450 | -0.19 | -0.75 | 0.855 | 0.915 | 1.000 | 23916 | tags=41%, list=44%, signal=73% | |
4271 | RESPONSE TO INTERLEUKIN-4 | 26 | -0.25 | -0.75 | 0.751 | 0.915 | 1.000 | 21567 | tags=38%, list=39%, signal=63% | |
4272 | REGULATION OF ENERGY HOMEOSTASIS | 46 | -0.21 | -0.75 | 0.837 | 0.915 | 1.000 | 37133 | tags=76%, list=68%, signal=237% | |
4273 | BILE ACID SIGNALING PATHWAY | 8 | -0.33 | -0.75 | 0.798 | 0.915 | 1.000 | 27648 | tags=63%, list=51%, signal=126% | |
4274 | VENTRICULAR CARDIAC MUSCLE TISSUE MORPHOGENESIS | 59 | -0.20 | -0.75 | 0.839 | 0.916 | 1.000 | 33973 | tags=59%, list=62%, signal=157% | |
4275 | CELLULAR RESPONSE TO LAMINAR FLUID SHEAR STRESS | 20 | -0.26 | -0.75 | 0.760 | 0.917 | 1.000 | 19583 | tags=40%, list=36%, signal=62% | |
4276 | POSITIVE REGULATION OF NUCLEOTIDE CATABOLIC PROCESS | 30 | -0.23 | -0.75 | 0.785 | 0.917 | 1.000 | 25775 | tags=53%, list=47%, signal=101% | |
4277 | CELLULAR PHOSPHATE ION HOMEOSTASIS | 11 | -0.28 | -0.75 | 0.782 | 0.917 | 1.000 | 33663 | tags=73%, list=62%, signal=189% | |
4278 | CELLULAR TRIVALENT INORGANIC ANION HOMEOSTASIS | 11 | -0.28 | -0.75 | 0.782 | 0.917 | 1.000 | 33663 | tags=73%, list=62%, signal=189% | |
4279 | POSITIVE REGULATION OF NITRIC OXIDE BIOSYNTHETIC PROCESS | 64 | -0.22 | -0.75 | 0.868 | 0.916 | 1.000 | 23143 | tags=41%, list=42%, signal=70% | |
4280 | POSITIVE REGULATION OF NITRIC OXIDE METABOLIC PROCESS | 64 | -0.22 | -0.75 | 0.868 | 0.916 | 1.000 | 23143 | tags=41%, list=42%, signal=70% | |
4281 | POSITIVE REGULATION OF PEPTIDYL-TYROSINE PHOSPHORYLATION | 261 | -0.18 | -0.75 | 0.834 | 0.917 | 1.000 | 26927 | tags=43%, list=49%, signal=85% | |
4282 | ESTABLISHMENT OF ENDOTHELIAL BARRIER | 68 | -0.21 | -0.75 | 0.824 | 0.916 | 1.000 | 28323 | tags=53%, list=52%, signal=110% | |
4283 | DNA METHYLATION INVOLVED IN GAMETE GENERATION | 22 | -0.25 | -0.75 | 0.793 | 0.916 | 1.000 | 24155 | tags=45%, list=44%, signal=81% | |
4284 | REGULATION OF PRODUCTION OF SMALL RNA INVOLVED IN GENE SILENCING BY RNA | 6 | -0.35 | -0.75 | 0.806 | 0.917 | 1.000 | 32076 | tags=83%, list=59%, signal=202% | |
4285 | POSITIVE REGULATION OF CD4-POSITIVE, ALPHA-BETA T CELL ACTIVATION | 40 | -0.24 | -0.75 | 0.760 | 0.917 | 1.000 | 28398 | tags=50%, list=52%, signal=104% | |
4286 | NON-CANONICAL WNT SIGNALING PATHWAY | 25 | -0.22 | -0.75 | 0.820 | 0.917 | 1.000 | 36274 | tags=64%, list=66%, signal=190% | |
4287 | POSITIVE REGULATION OF LYMPHOCYTE ACTIVATION | 433 | -0.19 | -0.75 | 0.867 | 0.917 | 1.000 | 27612 | tags=47%, list=51%, signal=95% | |
4288 | RESPONSE TO LEPTIN | 28 | -0.24 | -0.75 | 0.766 | 0.917 | 1.000 | 37133 | tags=79%, list=68%, signal=245% | |
4289 | SPERM-EGG RECOGNITION | 42 | -0.23 | -0.75 | 0.791 | 0.917 | 1.000 | 21050 | tags=38%, list=39%, signal=62% | |
4290 | KIDNEY MESENCHYME DEVELOPMENT | 21 | -0.24 | -0.75 | 0.768 | 0.918 | 1.000 | 32921 | tags=67%, list=60%, signal=167% | |
4291 | CELLULAR CALCIUM ION HOMEOSTASIS | 409 | -0.17 | -0.75 | 0.907 | 0.918 | 1.000 | 32671 | tags=55%, list=60%, signal=136% | |
4292 | FAT-SOLUBLE VITAMIN CATABOLIC PROCESS | 7 | -0.35 | -0.75 | 0.735 | 0.919 | 1.000 | 26960 | tags=57%, list=49%, signal=113% | |
4293 | REGULATION OF LYSOSOMAL LUMEN PH | 18 | -0.26 | -0.75 | 0.800 | 0.919 | 1.000 | 30883 | tags=67%, list=56%, signal=153% | |
4294 | POSITIVE REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 24 | -0.24 | -0.75 | 0.810 | 0.919 | 1.000 | 25822 | tags=54%, list=47%, signal=103% | |
4295 | REGULATION OF OLIGODENDROCYTE DIFFERENTIATION | 24 | -0.24 | -0.75 | 0.786 | 0.919 | 1.000 | 32533 | tags=67%, list=60%, signal=165% | |
4296 | BONE MINERALIZATION | 34 | -0.22 | -0.75 | 0.785 | 0.919 | 1.000 | 30219 | tags=56%, list=55%, signal=125% | |
4297 | UDP-N-ACETYLGLUCOSAMINE BIOSYNTHETIC PROCESS | 9 | -0.34 | -0.75 | 0.762 | 0.919 | 1.000 | 36016 | tags=100%, list=66%, signal=293% | |
4298 | FOREBRAIN NEURON DEVELOPMENT | 34 | -0.23 | -0.75 | 0.790 | 0.919 | 1.000 | 36712 | tags=74%, list=67%, signal=224% | |
4299 | REGULATION OF MHC CLASS I BIOSYNTHETIC PROCESS | 9 | -0.29 | -0.75 | 0.788 | 0.919 | 1.000 | 21147 | tags=44%, list=39%, signal=72% | |
4300 | POSITIVE REGULATION OF MHC CLASS I BIOSYNTHETIC PROCESS | 9 | -0.29 | -0.75 | 0.788 | 0.919 | 1.000 | 21147 | tags=44%, list=39%, signal=72% | |
4301 | CAMP METABOLIC PROCESS | 69 | -0.21 | -0.75 | 0.814 | 0.919 | 1.000 | 11449 | tags=22%, list=21%, signal=27% | |
4302 | N-ACETYLGLUCOSAMINE METABOLIC PROCESS | 16 | -0.27 | -0.75 | 0.794 | 0.919 | 1.000 | 34768 | tags=81%, list=64%, signal=223% | |
4303 | RESPONSE TO ACTIVITY | 13 | -0.28 | -0.75 | 0.797 | 0.919 | 1.000 | 7771 | tags=23%, list=14%, signal=27% | |
4304 | RESPONSE TO MUSCLE ACTIVITY | 13 | -0.28 | -0.75 | 0.797 | 0.918 | 1.000 | 7771 | tags=23%, list=14%, signal=27% | |
4305 | ORGAN FORMATION | 34 | -0.23 | -0.75 | 0.807 | 0.918 | 1.000 | 32287 | tags=62%, list=59%, signal=151% | |
4306 | NEGATIVE REGULATION OF INTERLEUKIN-6 SECRETION | 13 | -0.29 | -0.75 | 0.778 | 0.918 | 1.000 | 32004 | tags=77%, list=59%, signal=185% | |
4307 | RECEPTOR RECYCLING | 11 | -0.29 | -0.75 | 0.803 | 0.919 | 1.000 | 36279 | tags=91%, list=66%, signal=270% | |
4308 | CEREBELLUM MORPHOGENESIS | 28 | -0.22 | -0.75 | 0.797 | 0.919 | 1.000 | 33770 | tags=64%, list=62%, signal=168% | |
4309 | POSITIVE REGULATION OF CD4-POSITIVE, ALPHA-BETA T CELL DIFFERENTIATION | 32 | -0.24 | -0.75 | 0.773 | 0.919 | 1.000 | 28398 | tags=47%, list=52%, signal=97% | |
4310 | REGULATION OF SYNCYTIUM FORMATION BY PLASMA MEMBRANE FUSION | 42 | -0.27 | -0.75 | 0.768 | 0.919 | 1.000 | 16694 | tags=38%, list=31%, signal=55% | |
4311 | ALDEHYDE CATABOLIC PROCESS | 10 | -0.30 | -0.75 | 0.768 | 0.919 | 1.000 | 16489 | tags=40%, list=30%, signal=57% | |
4312 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER INVOLVED IN MYOCARDIAL PRECURSOR CELL DIFFERENTIATION | 16 | -0.27 | -0.75 | 0.742 | 0.920 | 1.000 | 5907 | tags=19%, list=11%, signal=21% | |
4313 | NEUTROPHIL MIGRATION | 48 | -0.27 | -0.75 | 0.784 | 0.920 | 1.000 | 17066 | tags=33%, list=31%, signal=48% | |
4314 | GLYCOSYL COMPOUND CATABOLIC PROCESS | 63 | -0.20 | -0.75 | 0.845 | 0.920 | 1.000 | 35532 | tags=73%, list=65%, signal=208% | |
4315 | OVULATION CYCLE | 47 | -0.22 | -0.75 | 0.830 | 0.920 | 1.000 | 6539 | tags=17%, list=12%, signal=19% | |
4316 | REGULATION OF TYPE 2 IMMUNE RESPONSE | 27 | -0.25 | -0.75 | 0.824 | 0.920 | 1.000 | 30991 | tags=56%, list=57%, signal=128% | |
4317 | ORGANIC CATION TRANSPORT | 22 | -0.23 | -0.75 | 0.845 | 0.920 | 1.000 | 16620 | tags=32%, list=30%, signal=46% | |
4318 | B CELL ACTIVATION | 159 | -0.19 | -0.75 | 0.889 | 0.920 | 1.000 | 29422 | tags=52%, list=54%, signal=111% | |
4319 | REGULATION OF T CELL DIFFERENTIATION IN THYMUS | 31 | -0.24 | -0.74 | 0.820 | 0.920 | 1.000 | 35416 | tags=74%, list=65%, signal=211% | |
4320 | REGULATION OF THYMOCYTE AGGREGATION | 31 | -0.24 | -0.74 | 0.820 | 0.920 | 1.000 | 35416 | tags=74%, list=65%, signal=211% | |
4321 | NEGATIVE REGULATION OF VOLTAGE-GATED CALCIUM CHANNEL ACTIVITY | 12 | -0.27 | -0.74 | 0.816 | 0.920 | 1.000 | 3680 | tags=17%, list=7%, signal=18% | |
4322 | REGULATION OF HYDROGEN PEROXIDE-INDUCED CELL DEATH | 33 | -0.22 | -0.74 | 0.871 | 0.920 | 1.000 | 9001 | tags=21%, list=16%, signal=25% | |
4323 | CORTICAL CYTOSKELETON ORGANIZATION | 52 | -0.22 | -0.74 | 0.763 | 0.920 | 1.000 | 30730 | tags=60%, list=56%, signal=136% | |
4324 | NEGATIVE REGULATION OF OSTEOBLAST PROLIFERATION | 14 | -0.27 | -0.74 | 0.802 | 0.919 | 1.000 | 37825 | tags=86%, list=69%, signal=278% | |
4325 | CERAMIDE TRANSPORT | 10 | -0.31 | -0.74 | 0.755 | 0.919 | 1.000 | 15079 | tags=40%, list=28%, signal=55% | |
4326 | SULFATE TRANSMEMBRANE TRANSPORT | 16 | -0.25 | -0.74 | 0.789 | 0.919 | 1.000 | 27021 | tags=56%, list=49%, signal=111% | |
4327 | INSULIN SECRETION | 29 | -0.24 | -0.74 | 0.800 | 0.919 | 1.000 | 21269 | tags=45%, list=39%, signal=73% | |
4328 | AXONAL FASCICULATION | 28 | -0.24 | -0.74 | 0.771 | 0.919 | 1.000 | 32712 | tags=64%, list=60%, signal=160% | |
4329 | REGULATION OF CILIUM BEAT FREQUENCY | 13 | -0.31 | -0.74 | 0.726 | 0.919 | 1.000 | 30179 | tags=77%, list=55%, signal=172% | |
4330 | PROTEIN LOCALIZATION TO SYNAPSE | 17 | -0.27 | -0.74 | 0.786 | 0.919 | 1.000 | 7877 | tags=18%, list=14%, signal=21% | |
4331 | EPIDERMIS DEVELOPMENT | 218 | -0.18 | -0.74 | 0.843 | 0.919 | 1.000 | 30758 | tags=53%, list=56%, signal=120% | |
4332 | GLYCOSAMINOGLYCAN CATABOLIC PROCESS | 137 | -0.20 | -0.74 | 0.776 | 0.919 | 1.000 | 20622 | tags=37%, list=38%, signal=60% | |
4333 | POSITIVE REGULATION OF PHOSPHOLIPASE A2 ACTIVITY | 14 | -0.27 | -0.74 | 0.745 | 0.920 | 1.000 | 21327 | tags=43%, list=39%, signal=70% | |
4334 | MOLYBDOPTERIN COFACTOR BIOSYNTHETIC PROCESS | 13 | -0.29 | -0.74 | 0.773 | 0.921 | 1.000 | 33872 | tags=85%, list=62%, signal=222% | |
4335 | MOLYBDOPTERIN COFACTOR METABOLIC PROCESS | 13 | -0.29 | -0.74 | 0.773 | 0.920 | 1.000 | 33872 | tags=85%, list=62%, signal=222% | |
4336 | PROSTHETIC GROUP METABOLIC PROCESS | 13 | -0.29 | -0.74 | 0.773 | 0.920 | 1.000 | 33872 | tags=85%, list=62%, signal=222% | |
4337 | ACTIVATION OF PHOSPHOLIPASE C ACTIVITY | 154 | -0.17 | -0.74 | 0.940 | 0.920 | 1.000 | 27369 | tags=46%, list=50%, signal=92% | |
4338 | REGULATION OF ERK1 AND ERK2 CASCADE | 372 | -0.18 | -0.74 | 0.903 | 0.920 | 1.000 | 30564 | tags=52%, list=56%, signal=116% | |
4339 | ADULT LOCOMOTORY BEHAVIOR | 31 | -0.21 | -0.74 | 0.819 | 0.920 | 1.000 | 16568 | tags=32%, list=30%, signal=46% | |
4340 | RESPONSE TO OSMOTIC STRESS | 66 | -0.22 | -0.74 | 0.856 | 0.920 | 1.000 | 30040 | tags=59%, list=55%, signal=131% | |
4341 | REGULATION OF MUSCLE CELL DIFFERENTIATION | 279 | -0.17 | -0.74 | 0.851 | 0.920 | 1.000 | 16716 | tags=29%, list=31%, signal=42% | |
4342 | EMBRYONIC DIGESTIVE TRACT DEVELOPMENT | 42 | -0.20 | -0.74 | 0.877 | 0.920 | 1.000 | 30616 | tags=55%, list=56%, signal=124% | |
4343 | REGULATION OF MITOTIC CELL CYCLE SPINDLE ASSEMBLY CHECKPOINT | 22 | -0.27 | -0.74 | 0.770 | 0.920 | 1.000 | 31967 | tags=73%, list=58%, signal=175% | |
4344 | REGULATION OF MITOTIC SPINDLE CHECKPOINT | 22 | -0.27 | -0.74 | 0.770 | 0.920 | 1.000 | 31967 | tags=73%, list=58%, signal=175% | |
4345 | GLUCOSAMINE-CONTAINING COMPOUND METABOLIC PROCESS | 19 | -0.26 | -0.74 | 0.801 | 0.920 | 1.000 | 35525 | tags=79%, list=65%, signal=225% | |
4346 | EPITHELIAL CELL MORPHOGENESIS | 45 | -0.22 | -0.74 | 0.801 | 0.919 | 1.000 | 17093 | tags=33%, list=31%, signal=48% | |
4347 | REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 105 | -0.20 | -0.74 | 0.847 | 0.920 | 1.000 | 24337 | tags=46%, list=45%, signal=82% | |
4348 | LYMPHOCYTE HOMEOSTASIS | 22 | -0.27 | -0.74 | 0.774 | 0.920 | 1.000 | 30021 | tags=64%, list=55%, signal=141% | |
4349 | AMEBOIDAL-TYPE CELL MIGRATION | 164 | -0.18 | -0.74 | 0.900 | 0.920 | 1.000 | 30627 | tags=54%, list=56%, signal=122% | |
4350 | ORGAN MORPHOGENESIS | 827 | -0.16 | -0.74 | 0.949 | 0.920 | 1.000 | 31201 | tags=51%, list=57%, signal=118% | |
4351 | IMMUNOGLOBULIN PRODUCTION | 66 | -0.21 | -0.74 | 0.833 | 0.919 | 1.000 | 26403 | tags=50%, list=48%, signal=97% | |
4352 | POSITIVE REGULATION OF RIG-I SIGNALING PATHWAY | 16 | -0.25 | -0.74 | 0.784 | 0.920 | 1.000 | 5285 | tags=19%, list=10%, signal=21% | |
4353 | NEGATIVE REGULATION OF INSULIN RECEPTOR SIGNALING PATHWAY | 50 | -0.22 | -0.74 | 0.809 | 0.920 | 1.000 | 29461 | tags=56%, list=54%, signal=121% | |
4354 | GLUTAMATE SECRETION | 59 | -0.20 | -0.74 | 0.861 | 0.920 | 1.000 | 17082 | tags=34%, list=31%, signal=49% | |
4355 | POSITIVE REGULATION OF NON-CANONICAL WNT SIGNALING PATHWAY | 21 | -0.26 | -0.74 | 0.763 | 0.920 | 1.000 | 37825 | tags=90%, list=69%, signal=293% | |
4356 | REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE BY RENIN-ANGIOTENSIN | 30 | -0.23 | -0.74 | 0.807 | 0.920 | 1.000 | 13274 | tags=27%, list=24%, signal=35% | |
4357 | POSITIVE REGULATION OF COFACTOR METABOLIC PROCESS | 28 | -0.23 | -0.74 | 0.799 | 0.920 | 1.000 | 24473 | tags=50%, list=45%, signal=90% | |
4358 | POSITIVE REGULATION OF COENZYME METABOLIC PROCESS | 28 | -0.23 | -0.74 | 0.799 | 0.919 | 1.000 | 24473 | tags=50%, list=45%, signal=90% | |
4359 | POSITIVE REGULATION OF CHEMOTAXIS | 182 | -0.19 | -0.74 | 0.843 | 0.920 | 1.000 | 15479 | tags=27%, list=28%, signal=38% | |
4360 | CELLULAR RESPONSE TO TOXIC SUBSTANCE | 12 | -0.28 | -0.74 | 0.769 | 0.920 | 1.000 | 30115 | tags=58%, list=55%, signal=130% | |
4361 | REGULATION OF ACTION POTENTIAL | 63 | -0.19 | -0.74 | 0.856 | 0.921 | 1.000 | 32594 | tags=59%, list=60%, signal=145% | |
4362 | POSITIVE REGULATION OF GLIOGENESIS | 38 | -0.22 | -0.74 | 0.785 | 0.921 | 1.000 | 32436 | tags=66%, list=59%, signal=162% | |
4363 | THROMBIN RECEPTOR SIGNALING PATHWAY | 13 | -0.31 | -0.74 | 0.781 | 0.921 | 1.000 | 12936 | tags=31%, list=24%, signal=40% | |
4364 | NUCLEOSIDE TRANSMEMBRANE TRANSPORT | 21 | -0.24 | -0.74 | 0.836 | 0.922 | 1.000 | 34355 | tags=62%, list=63%, signal=167% | |
4365 | POSITIVE REGULATION OF CELLULAR RESPONSE TO OXIDATIVE STRESS | 26 | -0.25 | -0.74 | 0.751 | 0.922 | 1.000 | 6539 | tags=23%, list=12%, signal=26% | |
4366 | POSITIVE REGULATION OF RESPONSE TO OXIDATIVE STRESS | 26 | -0.25 | -0.74 | 0.751 | 0.921 | 1.000 | 6539 | tags=23%, list=12%, signal=26% | |
4367 | REGULATION OF LEUKOCYTE ACTIVATION | 641 | -0.18 | -0.74 | 0.876 | 0.921 | 1.000 | 22721 | tags=38%, list=42%, signal=65% | |
4368 | TELENCEPHALON DEVELOPMENT | 199 | -0.19 | -0.74 | 0.888 | 0.921 | 1.000 | 31550 | tags=59%, list=58%, signal=139% | |
4369 | TISSUE MORPHOGENESIS | 550 | -0.16 | -0.74 | 0.954 | 0.921 | 1.000 | 32496 | tags=56%, list=59%, signal=136% | |
4370 | POSITIVE REGULATION OF PROTEIN AUTOPHOSPHORYLATION | 48 | -0.22 | -0.74 | 0.804 | 0.922 | 1.000 | 24797 | tags=50%, list=45%, signal=91% | |
4371 | NEGATIVE REGULATION OF ERK1 AND ERK2 CASCADE | 95 | -0.20 | -0.74 | 0.842 | 0.922 | 1.000 | 38245 | tags=75%, list=70%, signal=248% | |
4372 | MAMMARY GLAND DEVELOPMENT | 80 | -0.19 | -0.74 | 0.856 | 0.923 | 1.000 | 15718 | tags=28%, list=29%, signal=39% | |
4373 | OUTFLOW TRACT MORPHOGENESIS | 88 | -0.18 | -0.74 | 0.869 | 0.923 | 1.000 | 28394 | tags=47%, list=52%, signal=97% | |
4374 | MUSCLE FILAMENT SLIDING | 74 | -0.21 | -0.74 | 0.791 | 0.923 | 1.000 | 18936 | tags=34%, list=35%, signal=52% | |
4375 | ACTIN-MYOSIN FILAMENT SLIDING | 74 | -0.21 | -0.74 | 0.791 | 0.923 | 1.000 | 18936 | tags=34%, list=35%, signal=52% | |
4376 | REGULATION OF LEUKOCYTE MIGRATION | 184 | -0.20 | -0.74 | 0.856 | 0.922 | 1.000 | 28783 | tags=52%, list=53%, signal=109% | |
4377 | CELLULAR RESPONSE TO CALCIUM ION | 83 | -0.20 | -0.74 | 0.826 | 0.922 | 1.000 | 35211 | tags=69%, list=64%, signal=193% | |
4378 | POSITIVE REGULATION OF T CELL DIFFERENTIATION | 76 | -0.21 | -0.74 | 0.850 | 0.922 | 1.000 | 17788 | tags=32%, list=33%, signal=47% | |
4379 | PHOSPHATE ION TRANSPORT | 21 | -0.26 | -0.74 | 0.770 | 0.922 | 1.000 | 26973 | tags=48%, list=49%, signal=94% | |
4380 | PHOSPHATE ION TRANSMEMBRANE TRANSPORT | 21 | -0.26 | -0.74 | 0.770 | 0.922 | 1.000 | 26973 | tags=48%, list=49%, signal=94% | |
4381 | SENSORY PERCEPTION OF SOUR TASTE | 5 | -0.37 | -0.74 | 0.793 | 0.922 | 1.000 | 1578 | tags=20%, list=3%, signal=21% | |
4382 | NEGATIVE REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 79 | -0.20 | -0.74 | 0.778 | 0.923 | 1.000 | 35830 | tags=72%, list=66%, signal=209% | |
4383 | MAST CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 15 | -0.29 | -0.74 | 0.735 | 0.922 | 1.000 | 18565 | tags=40%, list=34%, signal=61% | |
4384 | MAST CELL DEGRANULATION | 15 | -0.29 | -0.74 | 0.735 | 0.922 | 1.000 | 18565 | tags=40%, list=34%, signal=61% | |
4385 | PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 90 | -0.20 | -0.74 | 0.841 | 0.922 | 1.000 | 23254 | tags=44%, list=43%, signal=77% | |
4386 | REGULATION OF MEMBRANE POTENTIAL | 429 | -0.16 | -0.74 | 0.950 | 0.922 | 1.000 | 23991 | tags=39%, list=44%, signal=70% | |
4387 | SECOND-MESSENGER-MEDIATED SIGNALING | 240 | -0.18 | -0.74 | 0.947 | 0.922 | 1.000 | 33386 | tags=56%, list=61%, signal=144% | |
4388 | POSITIVE REGULATION OF SODIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 30 | -0.21 | -0.74 | 0.823 | 0.922 | 1.000 | 25853 | tags=53%, list=47%, signal=101% | |
4389 | AORTA DEVELOPMENT | 48 | -0.20 | -0.74 | 0.801 | 0.922 | 1.000 | 31100 | tags=60%, list=57%, signal=140% | |
4390 | POSITIVE REGULATION OF CHEMOKINE PRODUCTION | 63 | -0.24 | -0.74 | 0.802 | 0.922 | 1.000 | 19886 | tags=41%, list=36%, signal=65% | |
4391 | EXCITATORY SYNAPSE ASSEMBLY | 25 | -0.24 | -0.74 | 0.776 | 0.922 | 1.000 | 19696 | tags=40%, list=36%, signal=62% | |
4392 | NEGATIVE REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 79 | -0.21 | -0.74 | 0.810 | 0.922 | 1.000 | 31854 | tags=61%, list=58%, signal=145% | |
4393 | BASE CONVERSION OR SUBSTITUTION EDITING | 21 | -0.23 | -0.74 | 0.815 | 0.922 | 1.000 | 1281 | tags=14%, list=2%, signal=15% | |
4394 | AXIS ELONGATION | 18 | -0.26 | -0.74 | 0.805 | 0.922 | 1.000 | 15718 | tags=33%, list=29%, signal=47% | |
4395 | MALE GONAD DEVELOPMENT | 68 | -0.20 | -0.73 | 0.838 | 0.922 | 1.000 | 31392 | tags=57%, list=57%, signal=135% | |
4396 | DEVELOPMENT OF PRIMARY MALE SEXUAL CHARACTERISTICS | 68 | -0.20 | -0.73 | 0.838 | 0.922 | 1.000 | 31392 | tags=57%, list=57%, signal=135% | |
4397 | NEGATIVE REGULATION OF FOCAL ADHESION ASSEMBLY | 52 | -0.22 | -0.73 | 0.779 | 0.922 | 1.000 | 34905 | tags=69%, list=64%, signal=191% | |
4398 | EPITHELIAL CELL DEVELOPMENT | 178 | -0.18 | -0.73 | 0.929 | 0.922 | 1.000 | 28323 | tags=50%, list=52%, signal=103% | |
4399 | REGULATION OF OXIDATIVE STRESS-INDUCED CELL DEATH | 81 | -0.22 | -0.73 | 0.832 | 0.921 | 1.000 | 37146 | tags=78%, list=68%, signal=242% | |
4400 | REGULATION OF CELLULAR SENESCENCE | 62 | -0.21 | -0.73 | 0.849 | 0.921 | 1.000 | 34776 | tags=66%, list=64%, signal=181% | |
4401 | POSITIVE REGULATION OF GLUCOSE TRANSPORT | 75 | -0.19 | -0.73 | 0.850 | 0.921 | 1.000 | 30970 | tags=59%, list=57%, signal=135% | |
4402 | POSITIVE REGULATION OF OSTEOCLAST DIFFERENTIATION | 17 | -0.27 | -0.73 | 0.764 | 0.921 | 1.000 | 25520 | tags=53%, list=47%, signal=99% | |
4403 | RETINOID METABOLIC PROCESS | 140 | -0.18 | -0.73 | 0.857 | 0.921 | 1.000 | 33967 | tags=59%, list=62%, signal=156% | |
4404 | REGULATION OF LYMPHOCYTE ACTIVATION | 577 | -0.18 | -0.73 | 0.871 | 0.922 | 1.000 | 22354 | tags=38%, list=41%, signal=63% | |
4405 | REGULATION OF MACROPHAGE DERIVED FOAM CELL DIFFERENTIATION | 59 | -0.21 | -0.73 | 0.800 | 0.921 | 1.000 | 37911 | tags=78%, list=69%, signal=254% | |
4406 | POSITIVE REGULATION OF INSULIN SECRETION INVOLVED IN CELLULAR RESPONSE TO GLUCOSE STIMULUS | 25 | -0.25 | -0.73 | 0.798 | 0.921 | 1.000 | 29286 | tags=64%, list=54%, signal=138% | |
4407 | REGULATION OF ESTABLISHMENT OF CELL POLARITY | 40 | -0.23 | -0.73 | 0.774 | 0.922 | 1.000 | 29484 | tags=63%, list=54%, signal=136% | |
4408 | SULFATION | 25 | -0.24 | -0.73 | 0.840 | 0.922 | 1.000 | 37972 | tags=88%, list=69%, signal=288% | |
4409 | REGULATION OF PHOSPHOLIPASE C ACTIVITY | 191 | -0.17 | -0.73 | 0.958 | 0.922 | 1.000 | 31445 | tags=53%, list=58%, signal=124% | |
4410 | DORSAL/VENTRAL AXIS SPECIFICATION | 24 | -0.23 | -0.73 | 0.835 | 0.922 | 1.000 | 31854 | tags=63%, list=58%, signal=150% | |
4411 | REGULATION OF CARDIAC MUSCLE CELL ACTION POTENTIAL | 48 | -0.20 | -0.73 | 0.858 | 0.922 | 1.000 | 32056 | tags=56%, list=59%, signal=136% | |
4412 | POLYOL TRANSPORT | 21 | -0.24 | -0.73 | 0.842 | 0.922 | 1.000 | 9973 | tags=24%, list=18%, signal=29% | |
4413 | MESENCHYME DEVELOPMENT | 215 | -0.17 | -0.73 | 0.883 | 0.922 | 1.000 | 30257 | tags=51%, list=55%, signal=113% | |
4414 | POSITIVE REGULATION OF GLUCOSE METABOLIC PROCESS | 59 | -0.19 | -0.73 | 0.880 | 0.922 | 1.000 | 35231 | tags=64%, list=64%, signal=181% | |
4415 | TRANSCRIPTION FROM MITOCHONDRIAL PROMOTER | 16 | -0.24 | -0.73 | 0.796 | 0.922 | 1.000 | 27805 | tags=56%, list=51%, signal=114% | |
4416 | REGULATION OF BROWN FAT CELL DIFFERENTIATION | 10 | -0.33 | -0.73 | 0.797 | 0.922 | 1.000 | 10308 | tags=30%, list=19%, signal=37% | |
4417 | REGULATION OF DNA DAMAGE RESPONSE, SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 77 | -0.21 | -0.73 | 0.812 | 0.922 | 1.000 | 29099 | tags=56%, list=53%, signal=119% | |
4418 | MEIOTIC NUCLEAR DIVISION | 131 | -0.18 | -0.73 | 0.936 | 0.922 | 1.000 | 10619 | tags=19%, list=19%, signal=24% | |
4419 | RETINA HOMEOSTASIS | 139 | -0.19 | -0.73 | 0.843 | 0.922 | 1.000 | 9784 | tags=19%, list=18%, signal=24% | |
4420 | REGULATION OF LYASE ACTIVITY | 128 | -0.19 | -0.73 | 0.860 | 0.923 | 1.000 | 20474 | tags=33%, list=37%, signal=52% | |
4421 | AMINOGLYCAN CATABOLIC PROCESS | 139 | -0.20 | -0.73 | 0.795 | 0.923 | 1.000 | 20622 | tags=37%, list=38%, signal=59% | |
4422 | SPINAL CORD MOTOR NEURON DIFFERENTIATION | 13 | -0.28 | -0.73 | 0.804 | 0.923 | 1.000 | 22892 | tags=54%, list=42%, signal=93% | |
4423 | REGULATION OF CALCIUM ION-DEPENDENT EXOCYTOSIS | 45 | -0.21 | -0.73 | 0.857 | 0.923 | 1.000 | 20698 | tags=38%, list=38%, signal=61% | |
4424 | POSITIVE REGULATION OF LEUKOCYTE ACTIVATION | 466 | -0.18 | -0.73 | 0.887 | 0.923 | 1.000 | 28398 | tags=48%, list=52%, signal=100% | |
4425 | NEGATIVE REGULATION OF T CELL DIFFERENTIATION | 49 | -0.20 | -0.73 | 0.882 | 0.923 | 1.000 | 30991 | tags=57%, list=57%, signal=132% | |
4426 | LENS MORPHOGENESIS IN CAMERA-TYPE EYE | 12 | -0.26 | -0.73 | 0.805 | 0.923 | 1.000 | 12728 | tags=33%, list=23%, signal=43% | |
4427 | INFLAMMATORY RESPONSE | 292 | -0.21 | -0.73 | 0.791 | 0.923 | 1.000 | 20800 | tags=37%, list=38%, signal=60% | |
4428 | REGULATION OF HEMATOPOIETIC STEM CELL PROLIFERATION | 19 | -0.26 | -0.73 | 0.812 | 0.923 | 1.000 | 37018 | tags=84%, list=68%, signal=261% | |
4429 | EPIDERMAL CELL DIFFERENTIATION | 80 | -0.20 | -0.73 | 0.846 | 0.923 | 1.000 | 20259 | tags=38%, list=37%, signal=59% | |
4430 | NEGATIVE REGULATION OF HEART CONTRACTION | 33 | -0.21 | -0.73 | 0.832 | 0.923 | 1.000 | 26074 | tags=45%, list=48%, signal=87% | |
4431 | REGULATION OF CARDIAC MUSCLE CELL DIFFERENTIATION | 23 | -0.24 | -0.73 | 0.805 | 0.923 | 1.000 | 32216 | tags=61%, list=59%, signal=148% | |
4432 | REGULATION OF ASTROCYTE DIFFERENTIATION | 23 | -0.25 | -0.73 | 0.733 | 0.923 | 1.000 | 27471 | tags=48%, list=50%, signal=96% | |
4433 | RESPONSE TO UV-A | 18 | -0.24 | -0.73 | 0.835 | 0.923 | 1.000 | 26495 | tags=44%, list=48%, signal=86% | |
4434 | TRIGLYCERIDE CATABOLIC PROCESS | 46 | -0.21 | -0.73 | 0.834 | 0.923 | 1.000 | 23759 | tags=46%, list=43%, signal=81% | |
4435 | FAT-SOLUBLE VITAMIN METABOLIC PROCESS | 114 | -0.19 | -0.73 | 0.828 | 0.923 | 1.000 | 21860 | tags=38%, list=40%, signal=63% | |
4436 | NEGATIVE REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 361 | -0.18 | -0.73 | 0.895 | 0.923 | 1.000 | 19061 | tags=34%, list=35%, signal=52% | |
4437 | REGULATION OF ORGAN GROWTH | 83 | -0.19 | -0.73 | 0.870 | 0.924 | 1.000 | 23437 | tags=40%, list=43%, signal=69% | |
4438 | LIPID DIGESTION | 40 | -0.21 | -0.73 | 0.828 | 0.924 | 1.000 | 32940 | tags=63%, list=60%, signal=157% | |
4439 | NEGATIVE REGULATION OF ADHERENS JUNCTION ORGANIZATION | 56 | -0.21 | -0.73 | 0.817 | 0.924 | 1.000 | 34905 | tags=68%, list=64%, signal=187% | |
4440 | NEGATIVE REGULATION OF SODIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 18 | -0.26 | -0.73 | 0.789 | 0.924 | 1.000 | 26088 | tags=56%, list=48%, signal=106% | |
4441 | CHONDROCYTE DEVELOPMENT | 17 | -0.28 | -0.73 | 0.764 | 0.924 | 1.000 | 37806 | tags=94%, list=69%, signal=305% | |
4442 | SINGLE ORGANISM CELL ADHESION | 610 | -0.18 | -0.73 | 0.874 | 0.924 | 1.000 | 33328 | tags=60%, list=61%, signal=152% | |
4443 | UREA METABOLIC PROCESS | 22 | -0.24 | -0.73 | 0.812 | 0.924 | 1.000 | 33749 | tags=68%, list=62%, signal=178% | |
4444 | NEGATIVE REGULATION OF CELLULAR COMPONENT MOVEMENT | 437 | -0.17 | -0.73 | 0.933 | 0.924 | 1.000 | 37042 | tags=66%, list=68%, signal=204% | |
4445 | NEGATIVE REGULATION OF LOCOMOTION | 460 | -0.17 | -0.73 | 0.929 | 0.924 | 1.000 | 37042 | tags=67%, list=68%, signal=207% | |
4446 | NEGATIVE REGULATION OF TUMOR NECROSIS FACTOR-MEDIATED SIGNALING PATHWAY | 24 | -0.23 | -0.73 | 0.833 | 0.924 | 1.000 | 34901 | tags=71%, list=64%, signal=196% | |
4447 | POLYKETIDE METABOLIC PROCESS | 18 | -0.29 | -0.73 | 0.752 | 0.924 | 1.000 | 33676 | tags=83%, list=62%, signal=217% | |
4448 | AMINOGLYCOSIDE ANTIBIOTIC METABOLIC PROCESS | 18 | -0.29 | -0.73 | 0.752 | 0.923 | 1.000 | 33676 | tags=83%, list=62%, signal=217% | |
4449 | DAUNORUBICIN METABOLIC PROCESS | 18 | -0.29 | -0.73 | 0.752 | 0.923 | 1.000 | 33676 | tags=83%, list=62%, signal=217% | |
4450 | DOXORUBICIN METABOLIC PROCESS | 18 | -0.29 | -0.73 | 0.752 | 0.923 | 1.000 | 33676 | tags=83%, list=62%, signal=217% | |
4451 | MUSCLE HYPERTROPHY | 42 | -0.21 | -0.73 | 0.843 | 0.923 | 1.000 | 32513 | tags=62%, list=59%, signal=153% | |
4452 | POSITIVE REGULATION OF EPIDERMAL GROWTH FACTOR-ACTIVATED RECEPTOR ACTIVITY | 16 | -0.27 | -0.73 | 0.817 | 0.923 | 1.000 | 10655 | tags=25%, list=19%, signal=31% | |
4453 | NEUROTRANSMITTER SECRETION | 156 | -0.18 | -0.73 | 0.900 | 0.924 | 1.000 | 36175 | tags=65%, list=66%, signal=193% | |
4454 | REGULATION OF STRIATED MUSCLE CONTRACTION | 151 | -0.17 | -0.73 | 0.932 | 0.924 | 1.000 | 26192 | tags=44%, list=48%, signal=84% | |
4455 | UROGENITAL SYSTEM DEVELOPMENT | 324 | -0.17 | -0.73 | 0.934 | 0.925 | 1.000 | 33362 | tags=58%, list=61%, signal=149% | |
4456 | CRANIOFACIAL SUTURE MORPHOGENESIS | 10 | -0.28 | -0.73 | 0.832 | 0.925 | 1.000 | 30153 | tags=70%, list=55%, signal=156% | |
4457 | PRIMARY ALCOHOL METABOLIC PROCESS | 59 | -0.20 | -0.73 | 0.826 | 0.925 | 1.000 | 6275 | tags=17%, list=11%, signal=19% | |
4458 | CENTRAL NERVOUS SYSTEM NEURON DEVELOPMENT | 88 | -0.19 | -0.73 | 0.864 | 0.924 | 1.000 | 21972 | tags=41%, list=40%, signal=68% | |
4459 | ALPHA-BETA T CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 43 | -0.23 | -0.73 | 0.807 | 0.924 | 1.000 | 36260 | tags=72%, list=66%, signal=214% | |
4460 | T CELL DIFFERENTIATION INVOLVED IN IMMUNE RESPONSE | 43 | -0.23 | -0.73 | 0.807 | 0.924 | 1.000 | 36260 | tags=72%, list=66%, signal=214% | |
4461 | ALPHA-BETA T CELL DIFFERENTIATION INVOLVED IN IMMUNE RESPONSE | 43 | -0.23 | -0.73 | 0.807 | 0.924 | 1.000 | 36260 | tags=72%, list=66%, signal=214% | |
4462 | NEGATIVE REGULATION OF NF-KAPPAB IMPORT INTO NUCLEUS | 41 | -0.23 | -0.73 | 0.850 | 0.924 | 1.000 | 29141 | tags=59%, list=53%, signal=125% | |
4463 | POSITIVE REGULATION OF LIPASE ACTIVITY | 243 | -0.17 | -0.73 | 0.923 | 0.924 | 1.000 | 27369 | tags=45%, list=50%, signal=89% | |
4464 | NEGATIVE REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 63 | -0.20 | -0.73 | 0.823 | 0.925 | 1.000 | 12819 | tags=25%, list=23%, signal=33% | |
4465 | REGULATION OF LEUKOCYTE MEDIATED CYTOTOXICITY | 88 | -0.21 | -0.72 | 0.845 | 0.925 | 1.000 | 17332 | tags=33%, list=32%, signal=48% | |
4466 | NEGATIVE REGULATION OF CARDIAC MUSCLE TISSUE GROWTH | 12 | -0.27 | -0.72 | 0.800 | 0.925 | 1.000 | 25188 | tags=50%, list=46%, signal=93% | |
4467 | NEGATIVE REGULATION OF HEART GROWTH | 12 | -0.27 | -0.72 | 0.800 | 0.925 | 1.000 | 25188 | tags=50%, list=46%, signal=93% | |
4468 | MESENCHYMAL CELL DIFFERENTIATION INVOLVED IN KIDNEY DEVELOPMENT | 9 | -0.29 | -0.72 | 0.826 | 0.925 | 1.000 | 35335 | tags=78%, list=65%, signal=220% | |
4469 | MESENCHYMAL CELL DIFFERENTIATION INVOLVED IN RENAL SYSTEM DEVELOPMENT | 9 | -0.29 | -0.72 | 0.826 | 0.925 | 1.000 | 35335 | tags=78%, list=65%, signal=220% | |
4470 | POSITIVE REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 110 | -0.18 | -0.72 | 0.909 | 0.925 | 1.000 | 30219 | tags=54%, list=55%, signal=120% | |
4471 | OTIC VESICLE DEVELOPMENT | 32 | -0.23 | -0.72 | 0.852 | 0.925 | 1.000 | 33971 | tags=66%, list=62%, signal=173% | |
4472 | NEGATIVE REGULATION OF GLUCOSE TRANSPORT | 29 | -0.25 | -0.72 | 0.819 | 0.925 | 1.000 | 13561 | tags=28%, list=25%, signal=37% | |
4473 | PEPTIDE SECRETION | 58 | -0.20 | -0.72 | 0.888 | 0.925 | 1.000 | 23143 | tags=40%, list=42%, signal=69% | |
4474 | PEPTIDE HORMONE SECRETION | 58 | -0.20 | -0.72 | 0.888 | 0.925 | 1.000 | 23143 | tags=40%, list=42%, signal=69% | |
4475 | ENDOTHELIAL CELL DEVELOPMENT | 77 | -0.21 | -0.72 | 0.860 | 0.926 | 1.000 | 28323 | tags=52%, list=52%, signal=108% | |
4476 | REGULATION OF OXIDATIVE STRESS-INDUCED NEURON DEATH | 25 | -0.26 | -0.72 | 0.802 | 0.926 | 1.000 | 6843 | tags=24%, list=13%, signal=27% | |
4477 | RESPONSE TO PROGESTERONE | 27 | -0.24 | -0.72 | 0.809 | 0.926 | 1.000 | 7789 | tags=19%, list=14%, signal=22% | |
4478 | DNA DAMAGE INDUCED PROTEIN PHOSPHORYLATION | 19 | -0.24 | -0.72 | 0.816 | 0.926 | 1.000 | 33364 | tags=74%, list=61%, signal=189% | |
4479 | DIACYLGLYCEROL METABOLIC PROCESS | 15 | -0.27 | -0.72 | 0.818 | 0.926 | 1.000 | 23100 | tags=47%, list=42%, signal=81% | |
4480 | POSITIVE REGULATION OF DOUBLE-STRAND BREAK REPAIR | 10 | -0.28 | -0.72 | 0.821 | 0.926 | 1.000 | 11907 | tags=30%, list=22%, signal=38% | |
4481 | PEPTIDYL-LYSINE TRIMETHYLATION | 46 | -0.24 | -0.72 | 0.785 | 0.926 | 1.000 | 31667 | tags=65%, list=58%, signal=155% | |
4482 | REGULATION OF RYANODINE-SENSITIVE CALCIUM-RELEASE CHANNEL ACTIVITY | 72 | -0.18 | -0.72 | 0.858 | 0.926 | 1.000 | 28642 | tags=56%, list=52%, signal=117% | |
4483 | NEGATIVE REGULATION OF CELL MOTILITY | 416 | -0.17 | -0.72 | 0.935 | 0.926 | 1.000 | 37042 | tags=67%, list=68%, signal=205% | |
4484 | POSITIVE REGULATION OF MEMBRANE DEPOLARIZATION | 16 | -0.26 | -0.72 | 0.807 | 0.926 | 1.000 | 38258 | tags=94%, list=70%, signal=312% | |
4485 | SMAD PROTEIN IMPORT INTO NUCLEUS | 14 | -0.27 | -0.72 | 0.793 | 0.926 | 1.000 | 28769 | tags=57%, list=53%, signal=121% | |
4486 | REGULATION OF RENAL SYSTEM PROCESS | 35 | -0.22 | -0.72 | 0.803 | 0.926 | 1.000 | 22100 | tags=40%, list=40%, signal=67% | |
4487 | LYMPHOCYTE CHEMOTAXIS | 23 | -0.29 | -0.72 | 0.771 | 0.926 | 1.000 | 13668 | tags=30%, list=25%, signal=41% | |
4488 | RESPONSE TO HEPATOCYTE GROWTH FACTOR | 14 | -0.27 | -0.72 | 0.819 | 0.926 | 1.000 | 17631 | tags=36%, list=32%, signal=53% | |
4489 | CELLULAR RESPONSE TO HEPATOCYTE GROWTH FACTOR STIMULUS | 14 | -0.27 | -0.72 | 0.819 | 0.926 | 1.000 | 17631 | tags=36%, list=32%, signal=53% | |
4490 | ALPHA-BETA T CELL DIFFERENTIATION | 50 | -0.22 | -0.72 | 0.833 | 0.926 | 1.000 | 31167 | tags=58%, list=57%, signal=135% | |
4491 | REGULATION OF PROTEIN MATURATION | 114 | -0.19 | -0.72 | 0.890 | 0.926 | 1.000 | 27885 | tags=52%, list=51%, signal=105% | |
4492 | REGULATION OF SINGLE STRANDED VIRAL RNA REPLICATION VIA DOUBLE STRANDED DNA INTERMEDIATE | 20 | -0.24 | -0.72 | 0.822 | 0.926 | 1.000 | 5883 | tags=20%, list=11%, signal=22% | |
4493 | REGULATION OF T-HELPER CELL DIFFERENTIATION | 37 | -0.22 | -0.72 | 0.803 | 0.926 | 1.000 | 30991 | tags=51%, list=57%, signal=118% | |
4494 | REGULATION OF MUSCLE SYSTEM PROCESS | 276 | -0.17 | -0.72 | 0.932 | 0.926 | 1.000 | 26192 | tags=43%, list=48%, signal=82% | |
4495 | FERTILIZATION | 92 | -0.19 | -0.72 | 0.898 | 0.927 | 1.000 | 21849 | tags=37%, list=40%, signal=61% | |
4496 | ENERGY HOMEOSTASIS | 18 | -0.26 | -0.72 | 0.821 | 0.927 | 1.000 | 37133 | tags=89%, list=68%, signal=277% | |
4497 | POSITIVE REGULATION OF ANTIGEN PROCESSING AND PRESENTATION | 14 | -0.27 | -0.72 | 0.767 | 0.927 | 1.000 | 22724 | tags=50%, list=42%, signal=86% | |
4498 | BARBED-END ACTIN FILAMENT CAPPING | 15 | -0.26 | -0.72 | 0.794 | 0.928 | 1.000 | 31885 | tags=67%, list=58%, signal=160% | |
4499 | SPECIFICATION OF ORGAN IDENTITY | 30 | -0.22 | -0.72 | 0.827 | 0.928 | 1.000 | 32287 | tags=60%, list=59%, signal=146% | |
4500 | NEGATIVE REGULATION OF CELL JUNCTION ASSEMBLY | 64 | -0.20 | -0.72 | 0.811 | 0.928 | 1.000 | 30488 | tags=59%, list=56%, signal=134% | |
4501 | APICAL JUNCTION ASSEMBLY | 98 | -0.20 | -0.72 | 0.801 | 0.929 | 1.000 | 30549 | tags=59%, list=56%, signal=134% | |
4502 | REGULATION OF METALLOENZYME ACTIVITY | 14 | -0.25 | -0.72 | 0.791 | 0.928 | 1.000 | 15238 | tags=36%, list=28%, signal=50% | |
4503 | RENAL SYSTEM DEVELOPMENT | 314 | -0.17 | -0.72 | 0.944 | 0.929 | 1.000 | 33362 | tags=58%, list=61%, signal=149% | |
4504 | HEART CONTRACTION | 105 | -0.17 | -0.72 | 0.880 | 0.928 | 1.000 | 26088 | tags=42%, list=48%, signal=80% | |
4505 | NEGATIVE REGULATION OF STEM CELL PROLIFERATION | 28 | -0.24 | -0.72 | 0.806 | 0.928 | 1.000 | 23136 | tags=46%, list=42%, signal=80% | |
4506 | SYMPATHETIC GANGLION DEVELOPMENT | 33 | -0.22 | -0.72 | 0.791 | 0.928 | 1.000 | 36790 | tags=76%, list=67%, signal=231% | |
4507 | CALCIUM ION IMPORT | 125 | -0.18 | -0.72 | 0.866 | 0.929 | 1.000 | 19562 | tags=32%, list=36%, signal=50% | |
4508 | POSITIVE REGULATION OF CHEMOKINE SECRETION | 9 | -0.30 | -0.72 | 0.788 | 0.929 | 1.000 | 37034 | tags=89%, list=68%, signal=275% | |
4509 | POSITIVE REGULATION OF PHOSPHOLIPASE ACTIVITY | 223 | -0.17 | -0.72 | 0.941 | 0.929 | 1.000 | 28634 | tags=48%, list=52%, signal=99% | |
4510 | THYROID GLAND DEVELOPMENT | 25 | -0.23 | -0.72 | 0.844 | 0.929 | 1.000 | 17992 | tags=32%, list=33%, signal=48% | |
4511 | RESPONSE TO SUPEROXIDE | 17 | -0.28 | -0.72 | 0.853 | 0.929 | 1.000 | 11036 | tags=29%, list=20%, signal=37% | |
4512 | REMOVAL OF SUPEROXIDE RADICALS | 17 | -0.28 | -0.72 | 0.853 | 0.929 | 1.000 | 11036 | tags=29%, list=20%, signal=37% | |
4513 | CELLULAR RESPONSE TO OXYGEN RADICAL | 17 | -0.28 | -0.72 | 0.853 | 0.929 | 1.000 | 11036 | tags=29%, list=20%, signal=37% | |
4514 | CELLULAR RESPONSE TO SUPEROXIDE | 17 | -0.28 | -0.72 | 0.853 | 0.928 | 1.000 | 11036 | tags=29%, list=20%, signal=37% | |
4515 | EMBRYONIC CAMERA-TYPE EYE MORPHOGENESIS | 26 | -0.22 | -0.72 | 0.826 | 0.928 | 1.000 | 19696 | tags=35%, list=36%, signal=54% | |
4516 | NEGATIVE REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 69 | -0.21 | -0.72 | 0.905 | 0.929 | 1.000 | 30969 | tags=58%, list=57%, signal=134% | |
4517 | SULFATE TRANSPORT | 18 | -0.24 | -0.72 | 0.815 | 0.929 | 1.000 | 27021 | tags=56%, list=49%, signal=110% | |
4518 | TOLERANCE INDUCTION | 12 | -0.32 | -0.72 | 0.842 | 0.929 | 1.000 | 26401 | tags=58%, list=48%, signal=113% | |
4519 | NEURON MATURATION | 35 | -0.21 | -0.72 | 0.854 | 0.929 | 1.000 | 16503 | tags=29%, list=30%, signal=41% | |
4520 | REGULATION OF ANGIOGENESIS | 393 | -0.17 | -0.72 | 0.946 | 0.929 | 1.000 | 33475 | tags=59%, list=61%, signal=150% | |
4521 | REGULATION OF ENDOTHELIAL CELL DIFFERENTIATION | 31 | -0.22 | -0.72 | 0.862 | 0.930 | 1.000 | 17823 | tags=35%, list=33%, signal=53% | |
4522 | NEGATIVE REGULATION OF VITAMIN D BIOSYNTHETIC PROCESS | 5 | -0.35 | -0.72 | 0.821 | 0.930 | 1.000 | 4070 | tags=20%, list=7%, signal=22% | |
4523 | LYMPHOCYTE ACTIVATION | 371 | -0.18 | -0.72 | 0.928 | 0.930 | 1.000 | 33293 | tags=60%, list=61%, signal=152% | |
4524 | NEGATIVE REGULATION OF MYOBLAST DIFFERENTIATION | 30 | -0.21 | -0.71 | 0.829 | 0.930 | 1.000 | 17579 | tags=30%, list=32%, signal=44% | |
4525 | REGULATION OF METALLOENDOPEPTIDASE ACTIVITY | 17 | -0.28 | -0.71 | 0.769 | 0.930 | 1.000 | 37349 | tags=82%, list=68%, signal=260% | |
4526 | LYMPHOCYTE AGGREGATION | 217 | -0.19 | -0.71 | 0.896 | 0.929 | 1.000 | 33453 | tags=63%, list=61%, signal=161% | |
4527 | NEGATIVE REGULATION OF CELL MIGRATION | 401 | -0.17 | -0.71 | 0.949 | 0.929 | 1.000 | 37042 | tags=67%, list=68%, signal=205% | |
4528 | NEGATIVE REGULATION OF JAK-STAT CASCADE | 29 | -0.22 | -0.71 | 0.839 | 0.929 | 1.000 | 35692 | tags=76%, list=65%, signal=218% | |
4529 | NEGATIVE REGULATION OF STAT CASCADE | 29 | -0.22 | -0.71 | 0.839 | 0.929 | 1.000 | 35692 | tags=76%, list=65%, signal=218% | |
4530 | NEGATIVE REGULATION OF CARDIAC MUSCLE CELL DIFFERENTIATION | 9 | -0.29 | -0.71 | 0.847 | 0.929 | 1.000 | 31642 | tags=67%, list=58%, signal=158% | |
4531 | CELLULAR DIVALENT INORGANIC CATION HOMEOSTASIS | 435 | -0.17 | -0.71 | 0.929 | 0.929 | 1.000 | 32671 | tags=55%, list=60%, signal=135% | |
4532 | POSITIVE REGULATION OF HUMORAL IMMUNE RESPONSE | 12 | -0.25 | -0.71 | 0.845 | 0.929 | 1.000 | 32672 | tags=58%, list=60%, signal=145% | |
4533 | POSITIVE REGULATION OF PHOSPHOLIPASE C ACTIVITY | 185 | -0.17 | -0.71 | 0.954 | 0.929 | 1.000 | 27369 | tags=45%, list=50%, signal=90% | |
4534 | NEGATIVE REGULATION OF ACTIN FILAMENT POLYMERIZATION | 44 | -0.21 | -0.71 | 0.882 | 0.929 | 1.000 | 19184 | tags=36%, list=35%, signal=56% | |
4535 | CELLULAR RESPONSE TO LEPTIN STIMULUS | 23 | -0.24 | -0.71 | 0.839 | 0.929 | 1.000 | 37133 | tags=83%, list=68%, signal=257% | |
4536 | SINGLE ORGANISMAL CELL-CELL ADHESION | 555 | -0.18 | -0.71 | 0.887 | 0.929 | 1.000 | 31286 | tags=55%, list=57%, signal=127% | |
4537 | POSITIVE REGULATION OF BEHAVIOR | 192 | -0.18 | -0.71 | 0.868 | 0.930 | 1.000 | 15479 | tags=27%, list=28%, signal=38% | |
4538 | LYMPHOCYTE COSTIMULATION | 167 | -0.19 | -0.71 | 0.860 | 0.931 | 1.000 | 27546 | tags=49%, list=50%, signal=97% | |
4539 | T CELL COSTIMULATION | 167 | -0.19 | -0.71 | 0.860 | 0.930 | 1.000 | 27546 | tags=49%, list=50%, signal=97% | |
4540 | POSITIVE REGULATION OF CYTOKINESIS | 73 | -0.18 | -0.71 | 0.921 | 0.931 | 1.000 | 32018 | tags=58%, list=59%, signal=139% | |
4541 | POSITIVE REGULATION OF VASCULOGENESIS | 18 | -0.24 | -0.71 | 0.850 | 0.931 | 1.000 | 35476 | tags=72%, list=65%, signal=206% | |
4542 | CD4-POSITIVE, ALPHA-BETA T CELL DIFFERENTIATION INVOLVED IN IMMUNE RESPONSE | 42 | -0.23 | -0.71 | 0.837 | 0.931 | 1.000 | 37233 | tags=74%, list=68%, signal=231% | |
4543 | T-HELPER CELL DIFFERENTIATION | 42 | -0.23 | -0.71 | 0.837 | 0.931 | 1.000 | 37233 | tags=74%, list=68%, signal=231% | |
4544 | NEGATIVE REGULATION OF PLATELET AGGREGATION | 12 | -0.27 | -0.71 | 0.812 | 0.931 | 1.000 | 16173 | tags=33%, list=30%, signal=47% | |
4545 | EPITHELIAL CELL MIGRATION | 122 | -0.18 | -0.71 | 0.919 | 0.931 | 1.000 | 19569 | tags=34%, list=36%, signal=52% | |
4546 | REGULATION OF SYNAPTIC TRANSMISSION, GABAERGIC | 26 | -0.23 | -0.71 | 0.851 | 0.931 | 1.000 | 11969 | tags=23%, list=22%, signal=30% | |
4547 | REGULATION OF PROTEIN PROCESSING | 111 | -0.18 | -0.71 | 0.911 | 0.931 | 1.000 | 27885 | tags=51%, list=51%, signal=105% | |
4548 | REGULATION OF LIPOPROTEIN METABOLIC PROCESS | 26 | -0.23 | -0.71 | 0.832 | 0.931 | 1.000 | 35928 | tags=77%, list=66%, signal=224% | |
4549 | REGULATION OF T CELL DIFFERENTIATION | 120 | -0.19 | -0.71 | 0.889 | 0.931 | 1.000 | 16993 | tags=30%, list=31%, signal=43% | |
4550 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 74 | -0.19 | -0.71 | 0.836 | 0.931 | 1.000 | 33239 | tags=64%, list=61%, signal=162% | |
4551 | REGULATION OF MUSCLE ADAPTATION | 80 | -0.19 | -0.71 | 0.921 | 0.931 | 1.000 | 26088 | tags=45%, list=48%, signal=86% | |
4552 | NEGATIVE REGULATION OF LEUKOCYTE MEDIATED CYTOTOXICITY | 24 | -0.30 | -0.71 | 0.811 | 0.931 | 1.000 | 13927 | tags=38%, list=25%, signal=50% | |
4553 | BLASTODERM SEGMENTATION | 18 | -0.29 | -0.71 | 0.762 | 0.931 | 1.000 | 5222 | tags=17%, list=10%, signal=18% | |
4554 | TRIPARTITE REGIONAL SUBDIVISION | 18 | -0.29 | -0.71 | 0.762 | 0.931 | 1.000 | 5222 | tags=17%, list=10%, signal=18% | |
4555 | ANTERIOR/POSTERIOR AXIS SPECIFICATION, EMBRYO | 18 | -0.29 | -0.71 | 0.762 | 0.931 | 1.000 | 5222 | tags=17%, list=10%, signal=18% | |
4556 | REGULATION OF CLATHRIN-MEDIATED ENDOCYTOSIS | 40 | -0.20 | -0.71 | 0.871 | 0.931 | 1.000 | 7920 | tags=20%, list=14%, signal=23% | |
4557 | STRIATED MUSCLE CONTRACTION | 138 | -0.16 | -0.71 | 0.890 | 0.930 | 1.000 | 24367 | tags=39%, list=45%, signal=70% | |
4558 | LYMPHOCYTE MIGRATION | 37 | -0.26 | -0.71 | 0.750 | 0.931 | 1.000 | 13668 | tags=30%, list=25%, signal=40% | |
4559 | OUTER DYNEIN ARM ASSEMBLY | 18 | -0.29 | -0.71 | 0.753 | 0.931 | 1.000 | 30179 | tags=72%, list=55%, signal=161% | |
4560 | CHONDROITIN SULFATE BIOSYNTHETIC PROCESS | 48 | -0.21 | -0.71 | 0.814 | 0.931 | 1.000 | 27573 | tags=54%, list=50%, signal=109% | |
4561 | PROTEOGLYCAN BIOSYNTHETIC PROCESS | 90 | -0.19 | -0.71 | 0.877 | 0.931 | 1.000 | 33584 | tags=63%, list=61%, signal=164% | |
4562 | T CELL ACTIVATION | 215 | -0.19 | -0.71 | 0.913 | 0.931 | 1.000 | 33453 | tags=62%, list=61%, signal=160% | |
4563 | T CELL AGGREGATION | 215 | -0.19 | -0.71 | 0.913 | 0.931 | 1.000 | 33453 | tags=62%, list=61%, signal=160% | |
4564 | ENDODERM DEVELOPMENT | 113 | -0.19 | -0.71 | 0.864 | 0.931 | 1.000 | 34362 | tags=60%, list=63%, signal=162% | |
4565 | PURINE RIBONUCLEOSIDE BISPHOSPHATE METABOLIC PROCESS | 42 | -0.20 | -0.71 | 0.898 | 0.931 | 1.000 | 37182 | tags=79%, list=68%, signal=245% | |
4566 | 3'-PHOSPHOADENOSINE 5'-PHOSPHOSULFATE METABOLIC PROCESS | 42 | -0.20 | -0.71 | 0.898 | 0.931 | 1.000 | 37182 | tags=79%, list=68%, signal=245% | |
4567 | GASTRULATION | 186 | -0.17 | -0.71 | 0.940 | 0.931 | 1.000 | 37561 | tags=69%, list=69%, signal=221% | |
4568 | POSITIVE REGULATION OF CELL ACTIVATION | 480 | -0.18 | -0.71 | 0.909 | 0.931 | 1.000 | 22721 | tags=38%, list=42%, signal=65% | |
4569 | KIDNEY DEVELOPMENT | 290 | -0.17 | -0.71 | 0.977 | 0.931 | 1.000 | 33362 | tags=58%, list=61%, signal=148% | |
4570 | REGULATION OF TRANSLATIONAL INITIATION BY EIF2 ALPHA PHOSPHORYLATION | 9 | -0.29 | -0.71 | 0.846 | 0.931 | 1.000 | 38694 | tags=100%, list=71%, signal=342% | |
4571 | REGULATION OF CATION CHANNEL ACTIVITY | 179 | -0.16 | -0.71 | 0.954 | 0.931 | 1.000 | 28867 | tags=50%, list=53%, signal=105% | |
4572 | POSITIVE REGULATION OF DENDRITIC CELL ANTIGEN PROCESSING AND PRESENTATION | 12 | -0.27 | -0.71 | 0.799 | 0.931 | 1.000 | 22724 | tags=50%, list=42%, signal=86% | |
4573 | REGULATION OF CYTOKINE SECRETION | 210 | -0.19 | -0.71 | 0.872 | 0.930 | 1.000 | 14706 | tags=28%, list=27%, signal=38% | |
4574 | NEGATIVE REGULATION OF INFLAMMATORY RESPONSE | 94 | -0.20 | -0.71 | 0.921 | 0.930 | 1.000 | 32790 | tags=61%, list=60%, signal=151% | |
4575 | REGULATION OF FEEDING BEHAVIOR | 17 | -0.24 | -0.71 | 0.827 | 0.930 | 1.000 | 19109 | tags=41%, list=35%, signal=63% | |
4576 | REGULATION OF HEART RATE | 132 | -0.17 | -0.71 | 0.928 | 0.930 | 1.000 | 28417 | tags=45%, list=52%, signal=94% | |
4577 | SENSORY PERCEPTION OF MECHANICAL STIMULUS | 174 | -0.17 | -0.71 | 0.904 | 0.930 | 1.000 | 24433 | tags=40%, list=45%, signal=71% | |
4578 | RNA 5'-END PROCESSING | 7 | -0.26 | -0.71 | 0.875 | 0.930 | 1.000 | 29956 | tags=71%, list=55%, signal=158% | |
4579 | VENTRICULAR SEPTUM DEVELOPMENT | 59 | -0.19 | -0.71 | 0.878 | 0.931 | 1.000 | 31100 | tags=54%, list=57%, signal=126% | |
4580 | VITAMIN D METABOLIC PROCESS | 16 | -0.24 | -0.71 | 0.859 | 0.931 | 1.000 | 38845 | tags=81%, list=71%, signal=281% | |
4581 | CALCIUM ION HOMEOSTASIS | 426 | -0.16 | -0.71 | 0.939 | 0.931 | 1.000 | 32671 | tags=54%, list=60%, signal=134% | |
4582 | NEURONAL ACTION POTENTIAL | 23 | -0.23 | -0.71 | 0.826 | 0.931 | 1.000 | 38258 | tags=83%, list=70%, signal=275% | |
4583 | AORTA MORPHOGENESIS | 47 | -0.20 | -0.71 | 0.818 | 0.931 | 1.000 | 31100 | tags=60%, list=57%, signal=138% | |
4584 | POSTSYNAPTIC MEMBRANE ASSEMBLY | 16 | -0.26 | -0.71 | 0.809 | 0.932 | 1.000 | 7877 | tags=19%, list=14%, signal=22% | |
4585 | C21-STEROID HORMONE BIOSYNTHETIC PROCESS | 19 | -0.22 | -0.71 | 0.852 | 0.931 | 1.000 | 27396 | tags=47%, list=50%, signal=95% | |
4586 | NEURAL PRECURSOR CELL PROLIFERATION | 83 | -0.19 | -0.71 | 0.894 | 0.932 | 1.000 | 17001 | tags=31%, list=31%, signal=45% | |
4587 | NEGATIVE REGULATION OF SYNAPTIC TRANSMISSION | 62 | -0.19 | -0.71 | 0.876 | 0.932 | 1.000 | 36946 | tags=77%, list=68%, signal=238% | |
4588 | FORMATION OF PRIMARY GERM LAYER | 165 | -0.18 | -0.71 | 0.909 | 0.932 | 1.000 | 34362 | tags=62%, list=63%, signal=166% | |
4589 | FEMALE GONAD DEVELOPMENT | 44 | -0.20 | -0.71 | 0.903 | 0.932 | 1.000 | 6539 | tags=16%, list=12%, signal=18% | |
4590 | DEVELOPMENT OF PRIMARY FEMALE SEXUAL CHARACTERISTICS | 44 | -0.20 | -0.71 | 0.903 | 0.932 | 1.000 | 6539 | tags=16%, list=12%, signal=18% | |
4591 | BODY FLUID SECRETION | 34 | -0.21 | -0.71 | 0.892 | 0.932 | 1.000 | 16765 | tags=29%, list=31%, signal=42% | |
4592 | REGULATION OF TRANSCRIPTION INVOLVED IN CELL FATE COMMITMENT | 31 | -0.21 | -0.71 | 0.902 | 0.932 | 1.000 | 22319 | tags=42%, list=41%, signal=71% | |
4593 | CARDIOVASCULAR SYSTEM DEVELOPMENT | 896 | -0.15 | -0.70 | 0.990 | 0.933 | 1.000 | 36427 | tags=65%, list=67%, signal=190% | |
4594 | CIRCULATORY SYSTEM DEVELOPMENT | 896 | -0.15 | -0.70 | 0.990 | 0.932 | 1.000 | 36427 | tags=65%, list=67%, signal=190% | |
4595 | POSITIVE REGULATION OF HETEROTYPIC CELL-CELL ADHESION | 32 | -0.27 | -0.70 | 0.798 | 0.932 | 1.000 | 20622 | tags=44%, list=38%, signal=70% | |
4596 | MUSCLE SYSTEM PROCESS | 469 | -0.15 | -0.70 | 0.951 | 0.932 | 1.000 | 23414 | tags=37%, list=43%, signal=64% | |
4597 | CELL DIFFERENTIATION INVOLVED IN EMBRYONIC PLACENTA DEVELOPMENT | 10 | -0.30 | -0.70 | 0.780 | 0.932 | 1.000 | 24866 | tags=60%, list=45%, signal=110% | |
4598 | BLOOD COAGULATION, FIBRIN CLOT FORMATION | 52 | -0.21 | -0.70 | 0.830 | 0.932 | 1.000 | 19289 | tags=35%, list=35%, signal=53% | |
4599 | REGULATION OF DNA ENDOREDUPLICATION | 20 | -0.27 | -0.70 | 0.780 | 0.932 | 1.000 | 34159 | tags=75%, list=62%, signal=200% | |
4600 | REGULATION OF CELL ACTIVATION | 692 | -0.17 | -0.70 | 0.923 | 0.932 | 1.000 | 22354 | tags=37%, list=41%, signal=62% | |
4601 | VASCULATURE DEVELOPMENT | 507 | -0.16 | -0.70 | 0.981 | 0.932 | 1.000 | 36835 | tags=67%, list=67%, signal=202% | |
4602 | NEGATIVE REGULATION BY HOST OF VIRAL PROCESS | 19 | -0.24 | -0.70 | 0.856 | 0.932 | 1.000 | 38694 | tags=79%, list=71%, signal=270% | |
4603 | VASCULAR SMOOTH MUSCLE CELL DEVELOPMENT | 12 | -0.28 | -0.70 | 0.803 | 0.932 | 1.000 | 27706 | tags=58%, list=51%, signal=118% | |
4604 | SENSORY ORGAN DEVELOPMENT | 391 | -0.16 | -0.70 | 0.981 | 0.932 | 1.000 | 30361 | tags=50%, list=56%, signal=111% | |
4605 | ANDROGEN METABOLIC PROCESS | 39 | -0.21 | -0.70 | 0.890 | 0.932 | 1.000 | 35798 | tags=69%, list=65%, signal=200% | |
4606 | CELLULAR RESPONSE TO INTERLEUKIN-1 | 85 | -0.19 | -0.70 | 0.857 | 0.932 | 1.000 | 23643 | tags=41%, list=43%, signal=72% | |
4607 | REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 30 | -0.21 | -0.70 | 0.889 | 0.932 | 1.000 | 30907 | tags=57%, list=57%, signal=130% | |
4608 | RESPONSE TO COPPER ION | 24 | -0.22 | -0.70 | 0.845 | 0.932 | 1.000 | 14129 | tags=29%, list=26%, signal=39% | |
4609 | POSITIVE REGULATION OF HEART RATE | 24 | -0.23 | -0.70 | 0.846 | 0.932 | 1.000 | 24337 | tags=38%, list=45%, signal=68% | |
4610 | POSITIVE REGULATION OF CELL-CELL ADHESION | 405 | -0.18 | -0.70 | 0.920 | 0.932 | 1.000 | 23916 | tags=40%, list=44%, signal=71% | |
4611 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO OXIDATIVE STRESS | 58 | -0.21 | -0.70 | 0.888 | 0.932 | 1.000 | 37133 | tags=76%, list=68%, signal=236% | |
4612 | NEGATIVE REGULATION OF RESPONSE TO OXIDATIVE STRESS | 58 | -0.21 | -0.70 | 0.888 | 0.931 | 1.000 | 37133 | tags=76%, list=68%, signal=236% | |
4613 | POSITIVE REGULATION OF NEURON MIGRATION | 15 | -0.23 | -0.70 | 0.844 | 0.932 | 1.000 | 35476 | tags=80%, list=65%, signal=228% | |
4614 | REGULATION OF CALCIDIOL 1-MONOOXYGENASE ACTIVITY | 11 | -0.33 | -0.70 | 0.815 | 0.932 | 1.000 | 14790 | tags=36%, list=27%, signal=50% | |
4615 | REGULATION OF MAINTENANCE OF SISTER CHROMATID COHESION | 17 | -0.29 | -0.70 | 0.768 | 0.932 | 1.000 | 34800 | tags=82%, list=64%, signal=226% | |
4616 | REGULATION OF MAINTENANCE OF MITOTIC SISTER CHROMATID COHESION | 17 | -0.29 | -0.70 | 0.768 | 0.932 | 1.000 | 34800 | tags=82%, list=64%, signal=226% | |
4617 | LEUKOCYTE ACTIVATION | 463 | -0.18 | -0.70 | 0.913 | 0.932 | 1.000 | 23285 | tags=40%, list=43%, signal=70% | |
4618 | POSITIVE REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 109 | -0.18 | -0.70 | 0.920 | 0.933 | 1.000 | 35838 | tags=64%, list=66%, signal=186% | |
4619 | REGULATION OF AXON EXTENSION INVOLVED IN AXON GUIDANCE | 19 | -0.23 | -0.70 | 0.849 | 0.933 | 1.000 | 29936 | tags=58%, list=55%, signal=128% | |
4620 | ENDOCHONDRAL BONE MORPHOGENESIS | 28 | -0.22 | -0.70 | 0.872 | 0.934 | 1.000 | 35838 | tags=68%, list=66%, signal=197% | |
4621 | CARDIOBLAST DIFFERENTIATION | 32 | -0.21 | -0.70 | 0.877 | 0.934 | 1.000 | 24508 | tags=41%, list=45%, signal=74% | |
4622 | REGULATION OF CARDIAC CONDUCTION | 158 | -0.16 | -0.70 | 0.906 | 0.934 | 1.000 | 16906 | tags=26%, list=31%, signal=37% | |
4623 | NEGATIVE REGULATION OF CHONDROCYTE DIFFERENTIATION | 24 | -0.22 | -0.70 | 0.891 | 0.933 | 1.000 | 16716 | tags=33%, list=31%, signal=48% | |
4624 | NEGATIVE REGULATION OF CARTILAGE DEVELOPMENT | 24 | -0.22 | -0.70 | 0.891 | 0.933 | 1.000 | 16716 | tags=33%, list=31%, signal=48% | |
4625 | REGULATION OF ENDOTHELIAL CELL MIGRATION | 285 | -0.17 | -0.70 | 0.966 | 0.933 | 1.000 | 36113 | tags=65%, list=66%, signal=191% | |
4626 | REGULATION OF CALCIUM-MEDIATED SIGNALING | 55 | -0.20 | -0.70 | 0.901 | 0.933 | 1.000 | 20950 | tags=40%, list=38%, signal=65% | |
4627 | REGULATION OF RESPONSE TO OSMOTIC STRESS | 12 | -0.25 | -0.70 | 0.855 | 0.933 | 1.000 | 29518 | tags=58%, list=54%, signal=127% | |
4628 | BIOLOGICAL ADHESION | 1182 | -0.16 | -0.70 | 0.967 | 0.933 | 1.000 | 31207 | tags=53%, list=57%, signal=121% | |
4629 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 52 | -0.21 | -0.70 | 0.853 | 0.934 | 1.000 | 33663 | tags=63%, list=62%, signal=165% | |
4630 | POSITIVE REGULATION OF CALCIUM ION-DEPENDENT EXOCYTOSIS | 22 | -0.23 | -0.70 | 0.844 | 0.934 | 1.000 | 22772 | tags=41%, list=42%, signal=70% | |
4631 | NEGATIVE REGULATION OF PROTEIN AUTOPHOSPHORYLATION | 17 | -0.24 | -0.70 | 0.844 | 0.935 | 1.000 | 22025 | tags=47%, list=40%, signal=79% | |
4632 | REGULATION OF INFLAMMATORY RESPONSE | 307 | -0.19 | -0.70 | 0.890 | 0.935 | 1.000 | 31228 | tags=57%, list=57%, signal=131% | |
4633 | POSITIVE REGULATION OF BMP SIGNALING PATHWAY | 42 | -0.20 | -0.70 | 0.847 | 0.934 | 1.000 | 36858 | tags=67%, list=67%, signal=204% | |
4634 | ZINC II ION TRANSMEMBRANE TRANSPORT | 29 | -0.22 | -0.70 | 0.835 | 0.935 | 1.000 | 25380 | tags=55%, list=46%, signal=103% | |
4635 | SPERM CAPACITATION | 14 | -0.27 | -0.70 | 0.856 | 0.935 | 1.000 | 1498 | tags=14%, list=3%, signal=15% | |
4636 | NEGATIVE REGULATION OF CALCIUM-MEDIATED SIGNALING | 14 | -0.27 | -0.70 | 0.810 | 0.935 | 1.000 | 18213 | tags=43%, list=33%, signal=64% | |
4637 | GLOMERULAR VISCERAL EPITHELIAL CELL DEVELOPMENT | 15 | -0.25 | -0.70 | 0.825 | 0.935 | 1.000 | 18177 | tags=33%, list=33%, signal=50% | |
4638 | REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 121 | -0.18 | -0.70 | 0.981 | 0.935 | 1.000 | 30361 | tags=51%, list=56%, signal=115% | |
4639 | REGULATION OF INTERFERON-GAMMA PRODUCTION | 132 | -0.21 | -0.70 | 0.844 | 0.936 | 1.000 | 28323 | tags=52%, list=52%, signal=107% | |
4640 | KIDNEY MORPHOGENESIS | 83 | -0.18 | -0.70 | 0.891 | 0.936 | 1.000 | 33291 | tags=57%, list=61%, signal=145% | |
4641 | ENDOCHONDRAL OSSIFICATION | 11 | -0.26 | -0.70 | 0.844 | 0.936 | 1.000 | 27588 | tags=55%, list=50%, signal=110% | |
4642 | REPLACEMENT OSSIFICATION | 11 | -0.26 | -0.70 | 0.844 | 0.936 | 1.000 | 27588 | tags=55%, list=50%, signal=110% | |
4643 | LENS DEVELOPMENT IN CAMERA-TYPE EYE | 32 | -0.20 | -0.70 | 0.891 | 0.936 | 1.000 | 36238 | tags=72%, list=66%, signal=213% | |
4644 | ENDOTHELIAL CELL MIGRATION | 95 | -0.18 | -0.70 | 0.904 | 0.937 | 1.000 | 19213 | tags=32%, list=35%, signal=49% | |
4645 | POSITIVE REGULATION OF ENDOTHELIAL CELL MIGRATION | 170 | -0.17 | -0.70 | 0.934 | 0.937 | 1.000 | 36113 | tags=65%, list=66%, signal=192% | |
4646 | EPITHELIUM MIGRATION | 123 | -0.18 | -0.70 | 0.932 | 0.937 | 1.000 | 19569 | tags=33%, list=36%, signal=52% | |
4647 | NEGATIVE REGULATION OF ANOIKIS | 55 | -0.19 | -0.69 | 0.897 | 0.938 | 1.000 | 32454 | tags=60%, list=59%, signal=147% | |
4648 | CELL ADHESION | 1167 | -0.16 | -0.69 | 0.969 | 0.938 | 1.000 | 31207 | tags=53%, list=57%, signal=121% | |
4649 | REPLICATIVE SENESCENCE | 24 | -0.23 | -0.69 | 0.858 | 0.938 | 1.000 | 6397 | tags=17%, list=12%, signal=19% | |
4650 | POSITIVE REGULATION OF TRANSCRIPTION REGULATORY REGION DNA BINDING | 27 | -0.22 | -0.69 | 0.881 | 0.938 | 1.000 | 10361 | tags=22%, list=19%, signal=27% | |
4651 | REGULATION OF MEMBRANE PROTEIN ECTODOMAIN PROTEOLYSIS | 37 | -0.23 | -0.69 | 0.893 | 0.937 | 1.000 | 29286 | tags=59%, list=54%, signal=128% | |
4652 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 88 | -0.18 | -0.69 | 0.879 | 0.937 | 1.000 | 30807 | tags=57%, list=56%, signal=130% | |
4653 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO CELL PERIPHERY | 88 | -0.18 | -0.69 | 0.879 | 0.937 | 1.000 | 30807 | tags=57%, list=56%, signal=130% | |
4654 | AROMATIC AMINO ACID FAMILY METABOLIC PROCESS | 52 | -0.20 | -0.69 | 0.866 | 0.937 | 1.000 | 32751 | tags=60%, list=60%, signal=149% | |
4655 | DIVALENT INORGANIC CATION HOMEOSTASIS | 469 | -0.16 | -0.69 | 0.965 | 0.937 | 1.000 | 32671 | tags=55%, list=60%, signal=134% | |
4656 | PEPTIDYL-TYROSINE DEPHOSPHORYLATION | 173 | -0.19 | -0.69 | 0.892 | 0.937 | 1.000 | 29461 | tags=54%, list=54%, signal=116% | |
4657 | REGULATION OF DENDRITIC CELL APOPTOTIC PROCESS | 15 | -0.28 | -0.69 | 0.842 | 0.937 | 1.000 | 35476 | tags=80%, list=65%, signal=228% | |
4658 | NEGATIVE REGULATION OF ALPHA-BETA T CELL DIFFERENTIATION | 26 | -0.21 | -0.69 | 0.865 | 0.937 | 1.000 | 30991 | tags=58%, list=57%, signal=133% | |
4659 | GLIAL CELL MIGRATION | 35 | -0.23 | -0.69 | 0.845 | 0.937 | 1.000 | 15881 | tags=31%, list=29%, signal=44% | |
4660 | LEUKOCYTE MIGRATION | 443 | -0.18 | -0.69 | 0.839 | 0.937 | 1.000 | 29654 | tags=53%, list=54%, signal=114% | |
4661 | ASPARTATE METABOLIC PROCESS | 7 | -0.29 | -0.69 | 0.839 | 0.937 | 1.000 | 21924 | tags=57%, list=40%, signal=95% | |
4662 | CELL-CELL ADHESION | 702 | -0.17 | -0.69 | 0.960 | 0.937 | 1.000 | 31207 | tags=53%, list=57%, signal=123% | |
4663 | POSITIVE REGULATION OF MEMBRANE PROTEIN ECTODOMAIN PROTEOLYSIS | 29 | -0.25 | -0.69 | 0.860 | 0.937 | 1.000 | 29286 | tags=62%, list=54%, signal=134% | |
4664 | BLASTOCYST FORMATION | 8 | -0.29 | -0.69 | 0.832 | 0.938 | 1.000 | 37884 | tags=88%, list=69%, signal=285% | |
4665 | POSITIVE REGULATION OF CELL ADHESION MEDIATED BY INTEGRIN | 31 | -0.22 | -0.69 | 0.852 | 0.938 | 1.000 | 21318 | tags=39%, list=39%, signal=63% | |
4666 | KIDNEY EPITHELIUM DEVELOPMENT | 142 | -0.17 | -0.69 | 0.902 | 0.938 | 1.000 | 29991 | tags=49%, list=55%, signal=107% | |
4667 | T CELL MIGRATION | 16 | -0.29 | -0.69 | 0.813 | 0.938 | 1.000 | 13668 | tags=31%, list=25%, signal=42% | |
4668 | RESPONSE TO ORGANOPHOSPHORUS | 133 | -0.18 | -0.69 | 0.907 | 0.938 | 1.000 | 20054 | tags=34%, list=37%, signal=53% | |
4669 | ENDODERMAL CELL DIFFERENTIATION | 98 | -0.18 | -0.69 | 0.869 | 0.938 | 1.000 | 34362 | tags=60%, list=63%, signal=162% | |
4670 | REGULATION OF TRANSMEMBRANE TRANSPORTER ACTIVITY | 342 | -0.15 | -0.69 | 0.981 | 0.938 | 1.000 | 20219 | tags=33%, list=37%, signal=52% | |
4671 | REGULATION OF MAST CELL DEGRANULATION | 29 | -0.23 | -0.69 | 0.809 | 0.938 | 1.000 | 9282 | tags=21%, list=17%, signal=25% | |
4672 | CYCLIC NUCLEOTIDE METABOLIC PROCESS | 108 | -0.18 | -0.69 | 0.900 | 0.939 | 1.000 | 11449 | tags=20%, list=21%, signal=26% | |
4673 | NEGATIVE REGULATION OF DNA ENDOREDUPLICATION | 17 | -0.28 | -0.69 | 0.787 | 0.939 | 1.000 | 7096 | tags=24%, list=13%, signal=27% | |
4674 | REGULATION OF ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 337 | -0.15 | -0.69 | 0.989 | 0.939 | 1.000 | 20219 | tags=33%, list=37%, signal=52% | |
4675 | PROTEIN POLYUFMYLATION | 11 | -0.28 | -0.69 | 0.808 | 0.939 | 1.000 | 27635 | tags=64%, list=51%, signal=129% | |
4676 | PROTEIN K69-LINKED UFMYLATION | 11 | -0.28 | -0.69 | 0.808 | 0.939 | 1.000 | 27635 | tags=64%, list=51%, signal=129% | |
4677 | DISTAL TUBULE DEVELOPMENT | 25 | -0.23 | -0.69 | 0.842 | 0.940 | 1.000 | 29315 | tags=52%, list=54%, signal=112% | |
4678 | REGULATION OF MUSCLE CONTRACTION | 209 | -0.16 | -0.69 | 0.943 | 0.940 | 1.000 | 24508 | tags=40%, list=45%, signal=72% | |
4679 | REGULATION OF INTERLEUKIN-6 BIOSYNTHETIC PROCESS | 18 | -0.25 | -0.69 | 0.843 | 0.940 | 1.000 | 21147 | tags=39%, list=39%, signal=63% | |
4680 | POSITIVE REGULATION OF STRIATED MUSCLE TISSUE DEVELOPMENT | 83 | -0.18 | -0.69 | 0.883 | 0.940 | 1.000 | 28184 | tags=46%, list=52%, signal=94% | |
4681 | POSITIVE REGULATION OF MUSCLE ORGAN DEVELOPMENT | 83 | -0.18 | -0.69 | 0.883 | 0.940 | 1.000 | 28184 | tags=46%, list=52%, signal=94% | |
4682 | BRAIN MORPHOGENESIS | 42 | -0.22 | -0.69 | 0.817 | 0.940 | 1.000 | 26579 | tags=57%, list=49%, signal=111% | |
4683 | POSITIVE REGULATION OF NUCLEOTIDE METABOLIC PROCESS | 202 | -0.17 | -0.69 | 0.952 | 0.941 | 1.000 | 30219 | tags=48%, list=55%, signal=107% | |
4684 | MUSCLE ORGAN MORPHOGENESIS | 86 | -0.17 | -0.69 | 0.895 | 0.941 | 1.000 | 32664 | tags=56%, list=60%, signal=138% | |
4685 | MUSCLE TISSUE MORPHOGENESIS | 86 | -0.17 | -0.69 | 0.895 | 0.941 | 1.000 | 32664 | tags=56%, list=60%, signal=138% | |
4686 | INSULIN SECRETION INVOLVED IN CELLULAR RESPONSE TO GLUCOSE STIMULUS | 9 | -0.30 | -0.69 | 0.833 | 0.941 | 1.000 | 21269 | tags=56%, list=39%, signal=91% | |
4687 | CELLULAR HORMONE METABOLIC PROCESS | 128 | -0.17 | -0.69 | 0.917 | 0.941 | 1.000 | 34824 | tags=63%, list=64%, signal=174% | |
4688 | ARTERY DEVELOPMENT | 95 | -0.17 | -0.69 | 0.915 | 0.941 | 1.000 | 36670 | tags=67%, list=67%, signal=204% | |
4689 | NEGATIVE REGULATION OF T CELL DIFFERENTIATION IN THYMUS | 15 | -0.24 | -0.69 | 0.865 | 0.941 | 1.000 | 35416 | tags=73%, list=65%, signal=208% | |
4690 | NEGATIVE REGULATION OF THYMOCYTE AGGREGATION | 15 | -0.24 | -0.69 | 0.865 | 0.941 | 1.000 | 35416 | tags=73%, list=65%, signal=208% | |
4691 | REGULATION OF SENSORY PERCEPTION OF PAIN | 15 | -0.27 | -0.69 | 0.834 | 0.941 | 1.000 | 14377 | tags=33%, list=26%, signal=45% | |
4692 | REGULATION OF SENSORY PERCEPTION | 15 | -0.27 | -0.69 | 0.834 | 0.941 | 1.000 | 14377 | tags=33%, list=26%, signal=45% | |
4693 | POSITIVE REGULATION OF POTASSIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 33 | -0.20 | -0.69 | 0.867 | 0.941 | 1.000 | 16903 | tags=30%, list=31%, signal=44% | |
4694 | GANGLION DEVELOPMENT | 35 | -0.21 | -0.69 | 0.795 | 0.941 | 1.000 | 36790 | tags=74%, list=67%, signal=227% | |
4695 | ENDODERM FORMATION | 103 | -0.18 | -0.69 | 0.867 | 0.941 | 1.000 | 34362 | tags=60%, list=63%, signal=162% | |
4696 | NEPHRON EPITHELIUM DEVELOPMENT | 118 | -0.17 | -0.69 | 0.909 | 0.941 | 1.000 | 33291 | tags=55%, list=61%, signal=141% | |
4697 | NOREPINEPHRINE METABOLIC PROCESS | 8 | -0.28 | -0.69 | 0.867 | 0.941 | 1.000 | 10361 | tags=25%, list=19%, signal=31% | |
4698 | REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 57 | -0.20 | -0.69 | 0.873 | 0.941 | 1.000 | 39506 | tags=79%, list=72%, signal=284% | |
4699 | EMBRYONIC CAMERA-TYPE EYE DEVELOPMENT | 28 | -0.21 | -0.69 | 0.846 | 0.942 | 1.000 | 19696 | tags=32%, list=36%, signal=50% | |
4700 | ETHER METABOLIC PROCESS | 15 | -0.27 | -0.69 | 0.811 | 0.942 | 1.000 | 24487 | tags=60%, list=45%, signal=109% | |
4701 | REGULATION OF GENE EXPRESSION BY GENETIC IMPRINTING | 12 | -0.26 | -0.69 | 0.867 | 0.942 | 1.000 | 20940 | tags=42%, list=38%, signal=68% | |
4702 | GENETIC IMPRINTING | 12 | -0.26 | -0.69 | 0.867 | 0.941 | 1.000 | 20940 | tags=42%, list=38%, signal=68% | |
4703 | NEGATIVE REGULATION OF BLOOD VESSEL MORPHOGENESIS | 153 | -0.17 | -0.69 | 0.901 | 0.941 | 1.000 | 37026 | tags=68%, list=68%, signal=210% | |
4704 | POSITIVE REGULATION OF CELL DIVISION | 190 | -0.17 | -0.69 | 0.949 | 0.941 | 1.000 | 30730 | tags=54%, list=56%, signal=122% | |
4705 | NEGATIVE REGULATION OF OXIDATIVE STRESS-INDUCED CELL DEATH | 56 | -0.21 | -0.69 | 0.904 | 0.941 | 1.000 | 37133 | tags=75%, list=68%, signal=234% | |
4706 | ARTERY MORPHOGENESIS | 85 | -0.17 | -0.68 | 0.925 | 0.941 | 1.000 | 36670 | tags=67%, list=67%, signal=203% | |
4707 | POSITIVE REGULATION OF TRANSPORTER ACTIVITY | 138 | -0.16 | -0.68 | 0.973 | 0.941 | 1.000 | 26835 | tags=47%, list=49%, signal=92% | |
4708 | APOLIPOPROTEIN A-I-MEDIATED SIGNALING PATHWAY | 16 | -0.24 | -0.68 | 0.876 | 0.941 | 1.000 | 37449 | tags=81%, list=68%, signal=258% | |
4709 | HORMONE CATABOLIC PROCESS | 8 | -0.29 | -0.68 | 0.854 | 0.941 | 1.000 | 13274 | tags=38%, list=24%, signal=50% | |
4710 | URATE METABOLIC PROCESS | 18 | -0.23 | -0.68 | 0.853 | 0.941 | 1.000 | 12504 | tags=22%, list=23%, signal=29% | |
4711 | STARTLE RESPONSE | 22 | -0.23 | -0.68 | 0.870 | 0.941 | 1.000 | 18246 | tags=41%, list=33%, signal=61% | |
4712 | REGULATION OF HEART RATE BY CARDIAC CONDUCTION | 45 | -0.19 | -0.68 | 0.911 | 0.941 | 1.000 | 32056 | tags=56%, list=59%, signal=134% | |
4713 | FOREBRAIN GENERATION OF NEURONS | 58 | -0.19 | -0.68 | 0.912 | 0.941 | 1.000 | 39211 | tags=78%, list=72%, signal=274% | |
4714 | REGULATION OF VASCULATURE DEVELOPMENT | 436 | -0.16 | -0.68 | 0.972 | 0.941 | 1.000 | 37033 | tags=66%, list=68%, signal=202% | |
4715 | GONAD DEVELOPMENT | 109 | -0.18 | -0.68 | 0.950 | 0.941 | 1.000 | 36628 | tags=65%, list=67%, signal=197% | |
4716 | CELLULAR RESPONSE TO STEROL | 31 | -0.20 | -0.68 | 0.879 | 0.941 | 1.000 | 31072 | tags=55%, list=57%, signal=127% | |
4717 | REGULATION OF SMOOTHENED SIGNALING PATHWAY | 89 | -0.17 | -0.68 | 0.933 | 0.941 | 1.000 | 19158 | tags=30%, list=35%, signal=47% | |
4718 | DETECTION OF LIGHT STIMULUS INVOLVED IN VISUAL PERCEPTION | 13 | -0.27 | -0.68 | 0.837 | 0.941 | 1.000 | 21224 | tags=38%, list=39%, signal=63% | |
4719 | DETECTION OF LIGHT STIMULUS INVOLVED IN SENSORY PERCEPTION | 13 | -0.27 | -0.68 | 0.837 | 0.941 | 1.000 | 21224 | tags=38%, list=39%, signal=63% | |
4720 | NEGATIVE REGULATION OF REPRODUCTIVE PROCESS | 41 | -0.21 | -0.68 | 0.851 | 0.940 | 1.000 | 37476 | tags=68%, list=69%, signal=217% | |
4721 | EMBRYONIC DIGESTIVE TRACT MORPHOGENESIS | 30 | -0.20 | -0.68 | 0.870 | 0.941 | 1.000 | 30616 | tags=53%, list=56%, signal=121% | |
4722 | BLOOD VESSEL DEVELOPMENT | 475 | -0.16 | -0.68 | 0.981 | 0.941 | 1.000 | 36835 | tags=67%, list=67%, signal=202% | |
4723 | NEGATIVE REGULATION OF LEUKOCYTE DIFFERENTIATION | 116 | -0.18 | -0.68 | 0.876 | 0.941 | 1.000 | 30021 | tags=50%, list=55%, signal=111% | |
4724 | CELLULAR RESPONSE TO COPPER ION | 14 | -0.26 | -0.68 | 0.819 | 0.941 | 1.000 | 14129 | tags=29%, list=26%, signal=39% | |
4725 | POSITIVE REGULATION OF CYTOKINE BIOSYNTHETIC PROCESS | 71 | -0.22 | -0.68 | 0.814 | 0.941 | 1.000 | 15474 | tags=30%, list=28%, signal=41% | |
4726 | NEGATIVE REGULATION OF OLIGODENDROCYTE DIFFERENTIATION | 18 | -0.23 | -0.68 | 0.835 | 0.942 | 1.000 | 26501 | tags=50%, list=48%, signal=97% | |
4727 | SOMITE DEVELOPMENT | 32 | -0.20 | -0.68 | 0.898 | 0.942 | 1.000 | 37102 | tags=69%, list=68%, signal=214% | |
4728 | NEGATIVE REGULATION OF INTERFERON-GAMMA PRODUCTION | 55 | -0.21 | -0.68 | 0.876 | 0.943 | 1.000 | 23310 | tags=40%, list=43%, signal=70% | |
4729 | REGULATION OF NUCLEOTIDE METABOLIC PROCESS | 318 | -0.16 | -0.68 | 0.957 | 0.943 | 1.000 | 30255 | tags=48%, list=55%, signal=108% | |
4730 | MITOTIC SISTER CHROMATID COHESION | 35 | -0.22 | -0.68 | 0.820 | 0.943 | 1.000 | 16669 | tags=37%, list=30%, signal=53% | |
4731 | POSITIVE REGULATION OF PHAGOCYTOSIS, ENGULFMENT | 8 | -0.30 | -0.68 | 0.867 | 0.942 | 1.000 | 10447 | tags=25%, list=19%, signal=31% | |
4732 | NEGATIVE REGULATION OF LYMPHOCYTE ACTIVATION | 154 | -0.19 | -0.68 | 0.888 | 0.942 | 1.000 | 22598 | tags=39%, list=41%, signal=66% | |
4733 | LOW-DENSITY LIPOPROTEIN PARTICLE CLEARANCE | 28 | -0.26 | -0.68 | 0.835 | 0.942 | 1.000 | 4636 | tags=18%, list=8%, signal=20% | |
4734 | NEGATIVE REGULATION OF LYMPHOCYTE DIFFERENTIATION | 57 | -0.19 | -0.68 | 0.901 | 0.943 | 1.000 | 36456 | tags=68%, list=67%, signal=205% | |
4735 | NEGATIVE REGULATION OF OSSIFICATION | 80 | -0.19 | -0.68 | 0.884 | 0.943 | 1.000 | 6904 | tags=18%, list=13%, signal=20% | |
4736 | RIBONUCLEOSIDE CATABOLIC PROCESS | 30 | -0.21 | -0.68 | 0.926 | 0.943 | 1.000 | 16813 | tags=33%, list=31%, signal=48% | |
4737 | CARDIAC MUSCLE CONTRACTION | 96 | -0.16 | -0.68 | 0.930 | 0.943 | 1.000 | 26088 | tags=42%, list=48%, signal=80% | |
4738 | RESPONSE TO ATP | 34 | -0.19 | -0.68 | 0.859 | 0.944 | 1.000 | 22571 | tags=38%, list=41%, signal=65% | |
4739 | ACTION POTENTIAL | 99 | -0.17 | -0.68 | 0.948 | 0.944 | 1.000 | 25853 | tags=42%, list=47%, signal=80% | |
4740 | POSITIVE REGULATION OF MUSCLE TISSUE DEVELOPMENT | 85 | -0.18 | -0.68 | 0.885 | 0.944 | 1.000 | 28184 | tags=46%, list=52%, signal=95% | |
4741 | REGULATION OF MHC CLASS II BIOSYNTHETIC PROCESS | 8 | -0.27 | -0.68 | 0.888 | 0.944 | 1.000 | 10308 | tags=25%, list=19%, signal=31% | |
4742 | POSITIVE REGULATION OF HOMOTYPIC CELL-CELL ADHESION | 369 | -0.17 | -0.68 | 0.933 | 0.944 | 1.000 | 24231 | tags=41%, list=44%, signal=73% | |
4743 | ASYMMETRIC NEUROBLAST DIVISION | 10 | -0.27 | -0.68 | 0.861 | 0.945 | 1.000 | 32260 | tags=70%, list=59%, signal=171% | |
4744 | REGULATION OF IMMATURE T CELL PROLIFERATION | 9 | -0.28 | -0.68 | 0.847 | 0.946 | 1.000 | 15092 | tags=33%, list=28%, signal=46% | |
4745 | REGULATION OF IMMATURE T CELL PROLIFERATION IN THYMUS | 9 | -0.28 | -0.68 | 0.847 | 0.946 | 1.000 | 15092 | tags=33%, list=28%, signal=46% | |
4746 | SIGNAL RELEASE | 233 | -0.16 | -0.68 | 0.949 | 0.945 | 1.000 | 23419 | tags=38%, list=43%, signal=67% | |
4747 | POSITIVE REGULATION OF REGULATORY T CELL DIFFERENTIATION | 14 | -0.26 | -0.68 | 0.838 | 0.945 | 1.000 | 16993 | tags=36%, list=31%, signal=52% | |
4748 | HETEROPHILIC CELL-CELL ADHESION VIA PLASMA MEMBRANE CELL ADHESION MOLECULES | 70 | -0.18 | -0.68 | 0.899 | 0.945 | 1.000 | 38037 | tags=73%, list=70%, signal=239% | |
4749 | POSITIVE REGULATION OF EXCITATORY POSTSYNAPTIC POTENTIAL | 47 | -0.19 | -0.68 | 0.886 | 0.946 | 1.000 | 18246 | tags=30%, list=33%, signal=45% | |
4750 | CHROMOSOME ORGANIZATION INVOLVED IN MEIOTIC CELL CYCLE | 19 | -0.23 | -0.68 | 0.873 | 0.946 | 1.000 | 5264 | tags=16%, list=10%, signal=17% | |
4751 | REGULATION OF LYMPHOCYTE DIFFERENTIATION | 144 | -0.18 | -0.68 | 0.905 | 0.946 | 1.000 | 30021 | tags=50%, list=55%, signal=111% | |
4752 | RIBOFLAVIN METABOLIC PROCESS | 11 | -0.26 | -0.68 | 0.855 | 0.946 | 1.000 | 5263 | tags=18%, list=10%, signal=20% | |
4753 | CELLULAR RESPONSE TO OSMOTIC STRESS | 36 | -0.21 | -0.68 | 0.894 | 0.946 | 1.000 | 33666 | tags=67%, list=62%, signal=173% | |
4754 | CD4-POSITIVE, ALPHA-BETA T CELL DIFFERENTIATION | 47 | -0.20 | -0.68 | 0.891 | 0.946 | 1.000 | 31167 | tags=57%, list=57%, signal=133% | |
4755 | CELLULAR RESPONSE TO CADMIUM ION | 10 | -0.31 | -0.68 | 0.813 | 0.947 | 1.000 | 36008 | tags=90%, list=66%, signal=264% | |
4756 | REGULATION OF CYTOKINE PRODUCTION INVOLVED IN INFLAMMATORY RESPONSE | 25 | -0.21 | -0.67 | 0.878 | 0.948 | 1.000 | 36647 | tags=76%, list=67%, signal=230% | |
4757 | REGULATION OF CARDIAC MUSCLE CELL CONTRACTION | 50 | -0.19 | -0.67 | 0.937 | 0.947 | 1.000 | 32056 | tags=54%, list=59%, signal=130% | |
4758 | RESPONSE TO NITRIC OXIDE | 22 | -0.21 | -0.67 | 0.893 | 0.948 | 1.000 | 33596 | tags=59%, list=61%, signal=153% | |
4759 | CORTICAL ACTIN CYTOSKELETON ORGANIZATION | 41 | -0.21 | -0.67 | 0.836 | 0.948 | 1.000 | 30730 | tags=59%, list=56%, signal=134% | |
4760 | SODIUM ION TRANSPORT | 172 | -0.16 | -0.67 | 0.939 | 0.948 | 1.000 | 24633 | tags=38%, list=45%, signal=70% | |
4761 | ADULT FEEDING BEHAVIOR | 10 | -0.28 | -0.67 | 0.848 | 0.949 | 1.000 | 15325 | tags=30%, list=28%, signal=42% | |
4762 | NUCLEOSIDE CATABOLIC PROCESS | 54 | -0.18 | -0.67 | 0.929 | 0.949 | 1.000 | 35532 | tags=70%, list=65%, signal=201% | |
4763 | RESPONSE TO BACTERIAL LIPOPROTEIN | 15 | -0.28 | -0.67 | 0.857 | 0.949 | 1.000 | 31155 | tags=73%, list=57%, signal=170% | |
4764 | LIPOXYGENASE PATHWAY | 21 | -0.26 | -0.67 | 0.845 | 0.949 | 1.000 | 36670 | tags=81%, list=67%, signal=246% | |
4765 | AMELOGENESIS | 27 | -0.22 | -0.67 | 0.857 | 0.950 | 1.000 | 21962 | tags=37%, list=40%, signal=62% | |
4766 | FOLIC ACID TRANSPORT | 16 | -0.24 | -0.67 | 0.853 | 0.950 | 1.000 | 27130 | tags=38%, list=50%, signal=74% | |
4767 | CARDIAC CHAMBER FORMATION | 23 | -0.22 | -0.67 | 0.875 | 0.950 | 1.000 | 27588 | tags=52%, list=50%, signal=105% | |
4768 | HORMONE METABOLIC PROCESS | 198 | -0.16 | -0.67 | 0.918 | 0.950 | 1.000 | 34824 | tags=60%, list=64%, signal=165% | |
4769 | POSITIVE REGULATION OF T CELL ACTIVATION | 350 | -0.17 | -0.67 | 0.948 | 0.950 | 1.000 | 27546 | tags=46%, list=50%, signal=92% | |
4770 | CELLULAR RESPONSE TO ESTRADIOL STIMULUS | 44 | -0.18 | -0.67 | 0.893 | 0.949 | 1.000 | 10442 | tags=20%, list=19%, signal=25% | |
4771 | POSITIVE REGULATION OF LEUKOCYTE CELL-CELL ADHESION | 368 | -0.17 | -0.67 | 0.933 | 0.950 | 1.000 | 24231 | tags=41%, list=44%, signal=73% | |
4772 | REGULATION OF G0 TO G1 TRANSITION | 10 | -0.27 | -0.67 | 0.865 | 0.950 | 1.000 | 17478 | tags=30%, list=32%, signal=44% | |
4773 | HEPOXILIN METABOLIC PROCESS | 7 | -0.32 | -0.67 | 0.829 | 0.950 | 1.000 | 31725 | tags=71%, list=58%, signal=170% | |
4774 | HEPOXILIN BIOSYNTHETIC PROCESS | 7 | -0.32 | -0.67 | 0.829 | 0.950 | 1.000 | 31725 | tags=71%, list=58%, signal=170% | |
4775 | CARDIAC VENTRICLE MORPHOGENESIS | 108 | -0.17 | -0.67 | 0.925 | 0.949 | 1.000 | 33973 | tags=56%, list=62%, signal=149% | |
4776 | POSITIVE REGULATION OF BONE RESORPTION | 11 | -0.27 | -0.67 | 0.861 | 0.949 | 1.000 | 25050 | tags=55%, list=46%, signal=101% | |
4777 | POSITIVE REGULATION OF BONE REMODELING | 11 | -0.27 | -0.67 | 0.861 | 0.949 | 1.000 | 25050 | tags=55%, list=46%, signal=101% | |
4778 | ASTROCYTE DEVELOPMENT | 22 | -0.23 | -0.67 | 0.822 | 0.950 | 1.000 | 32533 | tags=73%, list=60%, signal=180% | |
4779 | CELLULAR RESPONSE TO FATTY ACID | 55 | -0.20 | -0.67 | 0.908 | 0.950 | 1.000 | 28908 | tags=51%, list=53%, signal=108% | |
4780 | REGULATION OF GLIOGENESIS | 76 | -0.18 | -0.67 | 0.905 | 0.949 | 1.000 | 33089 | tags=59%, list=61%, signal=150% | |
4781 | REGULATION OF TOLL-LIKE RECEPTOR 3 SIGNALING PATHWAY | 20 | -0.24 | -0.67 | 0.869 | 0.950 | 1.000 | 19428 | tags=40%, list=36%, signal=62% | |
4782 | REGULATION OF PHOSPHOLIPASE ACTIVITY | 249 | -0.16 | -0.67 | 0.969 | 0.950 | 1.000 | 31445 | tags=52%, list=58%, signal=121% | |
4783 | FUCOSYLATION | 62 | -0.18 | -0.67 | 0.876 | 0.950 | 1.000 | 13766 | tags=26%, list=25%, signal=34% | |
4784 | METANEPHRIC EPITHELIUM DEVELOPMENT | 27 | -0.21 | -0.67 | 0.881 | 0.950 | 1.000 | 17093 | tags=30%, list=31%, signal=43% | |
4785 | MAST CELL ACTIVATION | 16 | -0.27 | -0.67 | 0.826 | 0.950 | 1.000 | 18565 | tags=38%, list=34%, signal=57% | |
4786 | BLOOD VESSEL MORPHOGENESIS | 405 | -0.15 | -0.67 | 0.981 | 0.950 | 1.000 | 36835 | tags=66%, list=67%, signal=200% | |
4787 | OMEGA-HYDROXYLASE P450 PATHWAY | 27 | -0.22 | -0.67 | 0.853 | 0.950 | 1.000 | 33525 | tags=70%, list=61%, signal=182% | |
4788 | REGULATION OF ENDOCRINE PROCESS | 44 | -0.20 | -0.67 | 0.913 | 0.950 | 1.000 | 30540 | tags=52%, list=56%, signal=118% | |
4789 | DERMATAN SULFATE PROTEOGLYCAN METABOLIC PROCESS | 44 | -0.21 | -0.67 | 0.861 | 0.950 | 1.000 | 37972 | tags=73%, list=69%, signal=238% | |
4790 | T CELL DIFFERENTIATION | 122 | -0.18 | -0.67 | 0.953 | 0.950 | 1.000 | 33770 | tags=61%, list=62%, signal=158% | |
4791 | POSITIVE REGULATION OF RECEPTOR RECYCLING | 17 | -0.24 | -0.67 | 0.874 | 0.950 | 1.000 | 27749 | tags=59%, list=51%, signal=119% | |
4792 | GLYCEROL ETHER METABOLIC PROCESS | 14 | -0.27 | -0.67 | 0.804 | 0.950 | 1.000 | 39801 | tags=100%, list=73%, signal=367% | |
4793 | ETHER LIPID METABOLIC PROCESS | 14 | -0.27 | -0.67 | 0.804 | 0.950 | 1.000 | 39801 | tags=100%, list=73%, signal=367% | |
4794 | GRANULOCYTE CHEMOTAXIS | 61 | -0.22 | -0.67 | 0.863 | 0.950 | 1.000 | 17066 | tags=30%, list=31%, signal=43% | |
4795 | CGMP BIOSYNTHETIC PROCESS | 18 | -0.23 | -0.67 | 0.861 | 0.950 | 1.000 | 24421 | tags=44%, list=45%, signal=80% | |
4796 | ORGAN GROWTH | 79 | -0.17 | -0.67 | 0.945 | 0.950 | 1.000 | 26563 | tags=44%, list=49%, signal=86% | |
4797 | REGULATION OF STEM CELL PROLIFERATION | 133 | -0.17 | -0.67 | 0.960 | 0.950 | 1.000 | 37018 | tags=67%, list=68%, signal=207% | |
4798 | REGULATION OF URINE VOLUME | 18 | -0.23 | -0.67 | 0.872 | 0.950 | 1.000 | 39043 | tags=78%, list=71%, signal=272% | |
4799 | LEUKOCYTE AGGREGATION | 241 | -0.19 | -0.67 | 0.877 | 0.950 | 1.000 | 21574 | tags=39%, list=39%, signal=65% | |
4800 | REGULATION OF INTERLEUKIN-10 PRODUCTION | 64 | -0.20 | -0.67 | 0.887 | 0.950 | 1.000 | 25520 | tags=45%, list=47%, signal=85% | |
4801 | NEGATIVE REGULATION OF PROTEIN SECRETION | 146 | -0.17 | -0.67 | 0.946 | 0.950 | 1.000 | 28741 | tags=48%, list=53%, signal=101% | |
4802 | NEGATIVE REGULATION OF ANGIOGENESIS | 148 | -0.17 | -0.67 | 0.916 | 0.950 | 1.000 | 37026 | tags=68%, list=68%, signal=211% | |
4803 | NEGATIVE REGULATION OF VASCULATURE DEVELOPMENT | 162 | -0.17 | -0.67 | 0.931 | 0.950 | 1.000 | 37026 | tags=67%, list=68%, signal=208% | |
4804 | EMBRYONIC EYE MORPHOGENESIS | 40 | -0.19 | -0.67 | 0.908 | 0.950 | 1.000 | 25268 | tags=43%, list=46%, signal=79% | |
4805 | PROTEIN IMPORT INTO NUCLEUS, TRANSLOCATION | 48 | -0.21 | -0.67 | 0.885 | 0.950 | 1.000 | 23981 | tags=46%, list=44%, signal=82% | |
4806 | CARDIAC VENTRICLE FORMATION | 20 | -0.22 | -0.67 | 0.868 | 0.950 | 1.000 | 27588 | tags=55%, list=50%, signal=111% | |
4807 | TISSUE MIGRATION | 130 | -0.17 | -0.67 | 0.957 | 0.950 | 1.000 | 19569 | tags=32%, list=36%, signal=50% | |
4808 | NEGATIVE REGULATION OF SPROUTING ANGIOGENESIS | 28 | -0.21 | -0.66 | 0.866 | 0.952 | 1.000 | 22241 | tags=43%, list=41%, signal=72% | |
4809 | REGULATION OF CARDIAC MUSCLE CONTRACTION BY CALCIUM ION SIGNALING | 55 | -0.18 | -0.66 | 0.939 | 0.951 | 1.000 | 27995 | tags=47%, list=51%, signal=97% | |
4810 | FUSION OF SPERM TO EGG PLASMA MEMBRANE | 7 | -0.29 | -0.66 | 0.867 | 0.952 | 1.000 | 20796 | tags=43%, list=38%, signal=69% | |
4811 | CARDIAC VENTRICLE DEVELOPMENT | 127 | -0.16 | -0.66 | 0.942 | 0.951 | 1.000 | 33973 | tags=56%, list=62%, signal=147% | |
4812 | MACROMOLECULAR COMPLEX REMODELING | 42 | -0.21 | -0.66 | 0.841 | 0.952 | 1.000 | 16531 | tags=29%, list=30%, signal=41% | |
4813 | PROTEIN-LIPID COMPLEX REMODELING | 42 | -0.21 | -0.66 | 0.841 | 0.952 | 1.000 | 16531 | tags=29%, list=30%, signal=41% | |
4814 | PLASMA LIPOPROTEIN PARTICLE REMODELING | 42 | -0.21 | -0.66 | 0.841 | 0.951 | 1.000 | 16531 | tags=29%, list=30%, signal=41% | |
4815 | RESPONSE TO LAMINAR FLUID SHEAR STRESS | 29 | -0.21 | -0.66 | 0.880 | 0.952 | 1.000 | 21536 | tags=38%, list=39%, signal=63% | |
4816 | REGULATION OF SYNAPSE ORGANIZATION | 103 | -0.17 | -0.66 | 0.916 | 0.953 | 1.000 | 18655 | tags=33%, list=34%, signal=50% | |
4817 | POSITIVE REGULATION OF ICOSANOID SECRETION | 17 | -0.25 | -0.66 | 0.882 | 0.953 | 1.000 | 28880 | tags=59%, list=53%, signal=125% | |
4818 | POSITIVE REGULATION OF FATTY ACID TRANSPORT | 17 | -0.25 | -0.66 | 0.882 | 0.953 | 1.000 | 28880 | tags=59%, list=53%, signal=125% | |
4819 | ENDOCARDIAL CUSHION DEVELOPMENT | 38 | -0.19 | -0.66 | 0.902 | 0.953 | 1.000 | 12962 | tags=24%, list=24%, signal=31% | |
4820 | VENTRAL SPINAL CORD DEVELOPMENT | 24 | -0.22 | -0.66 | 0.884 | 0.953 | 1.000 | 40558 | tags=92%, list=74%, signal=355% | |
4821 | PROTEIN DEGLUTAMYLATION | 17 | -0.24 | -0.66 | 0.856 | 0.953 | 1.000 | 41416 | tags=100%, list=76%, signal=412% | |
4822 | PLASMA MEMBRANE RAFT ASSEMBLY | 13 | -0.24 | -0.66 | 0.869 | 0.954 | 1.000 | 17355 | tags=38%, list=32%, signal=56% | |
4823 | PLASMA MEMBRANE RAFT ORGANIZATION | 13 | -0.24 | -0.66 | 0.869 | 0.953 | 1.000 | 17355 | tags=38%, list=32%, signal=56% | |
4824 | POSITIVE REGULATION OF MITOCHONDRIAL MEMBRANE PERMEABILITY INVOLVED IN APOPTOTIC PROCESS | 13 | -0.27 | -0.66 | 0.846 | 0.953 | 1.000 | 26545 | tags=62%, list=49%, signal=120% | |
4825 | MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN PROGRAMMED CELL DEATH | 13 | -0.27 | -0.66 | 0.846 | 0.953 | 1.000 | 26545 | tags=62%, list=49%, signal=120% | |
4826 | REGULATION OF SKELETAL MUSCLE TISSUE DEVELOPMENT | 59 | -0.18 | -0.66 | 0.920 | 0.953 | 1.000 | 6485 | tags=15%, list=12%, signal=17% | |
4827 | POSITIVE REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 39 | -0.20 | -0.66 | 0.913 | 0.954 | 1.000 | 42299 | tags=95%, list=77%, signal=419% | |
4828 | REGULATION OF TRANSPORTER ACTIVITY | 377 | -0.15 | -0.66 | 0.996 | 0.954 | 1.000 | 20219 | tags=33%, list=37%, signal=52% | |
4829 | INTERLEUKIN-6-MEDIATED SIGNALING PATHWAY | 24 | -0.25 | -0.66 | 0.794 | 0.954 | 1.000 | 12861 | tags=29%, list=24%, signal=38% | |
4830 | GOLGI DISASSEMBLY | 14 | -0.26 | -0.66 | 0.833 | 0.954 | 1.000 | 39446 | tags=93%, list=72%, signal=333% | |
4831 | POLY-N-ACETYLLACTOSAMINE METABOLIC PROCESS | 6 | -0.29 | -0.66 | 0.882 | 0.954 | 1.000 | 18862 | tags=33%, list=34%, signal=51% | |
4832 | POLY-N-ACETYLLACTOSAMINE BIOSYNTHETIC PROCESS | 6 | -0.29 | -0.66 | 0.882 | 0.954 | 1.000 | 18862 | tags=33%, list=34%, signal=51% | |
4833 | BICELLULAR TIGHT JUNCTION ASSEMBLY | 86 | -0.18 | -0.66 | 0.873 | 0.954 | 1.000 | 30549 | tags=58%, list=56%, signal=132% | |
4834 | REGULATION OF T CELL PROLIFERATION | 176 | -0.18 | -0.66 | 0.931 | 0.954 | 1.000 | 24197 | tags=41%, list=44%, signal=73% | |
4835 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT1 PROTEIN | 29 | -0.21 | -0.66 | 0.899 | 0.954 | 1.000 | 38993 | tags=79%, list=71%, signal=276% | |
4836 | STEROID CATABOLIC PROCESS | 29 | -0.20 | -0.66 | 0.909 | 0.954 | 1.000 | 39540 | tags=83%, list=72%, signal=299% | |
4837 | REGULATION OF LIPASE ACTIVITY | 280 | -0.15 | -0.66 | 0.961 | 0.954 | 1.000 | 29650 | tags=48%, list=54%, signal=103% | |
4838 | MICROVILLUS ASSEMBLY | 25 | -0.23 | -0.66 | 0.811 | 0.954 | 1.000 | 35476 | tags=76%, list=65%, signal=216% | |
4839 | MICROVILLUS ORGANIZATION | 25 | -0.23 | -0.66 | 0.811 | 0.954 | 1.000 | 35476 | tags=76%, list=65%, signal=216% | |
4840 | CHROMOSOME SEPARATION | 22 | -0.20 | -0.66 | 0.902 | 0.954 | 1.000 | 37620 | tags=64%, list=69%, signal=204% | |
4841 | NEUROMUSCULAR PROCESS CONTROLLING BALANCE | 34 | -0.19 | -0.66 | 0.871 | 0.954 | 1.000 | 11632 | tags=21%, list=21%, signal=26% | |
4842 | MRNA CIS SPLICING, VIA SPLICEOSOME | 20 | -0.25 | -0.66 | 0.827 | 0.954 | 1.000 | 23808 | tags=50%, list=44%, signal=89% | |
4843 | REGULATION OF COLLATERAL SPROUTING | 12 | -0.25 | -0.66 | 0.842 | 0.954 | 1.000 | 40841 | tags=92%, list=75%, signal=362% | |
4844 | HYALURONAN METABOLIC PROCESS | 48 | -0.21 | -0.66 | 0.872 | 0.955 | 1.000 | 20622 | tags=40%, list=38%, signal=63% | |
4845 | LEUKOCYTE CELL-CELL ADHESION | 296 | -0.17 | -0.66 | 0.920 | 0.955 | 1.000 | 31286 | tags=56%, list=57%, signal=130% | |
4846 | BLOOD VESSEL REMODELING | 25 | -0.21 | -0.66 | 0.908 | 0.955 | 1.000 | 33770 | tags=68%, list=62%, signal=178% | |
4847 | CARBOHYDRATE TRANSMEMBRANE TRANSPORT | 33 | -0.22 | -0.66 | 0.924 | 0.956 | 1.000 | 27305 | tags=52%, list=50%, signal=103% | |
4848 | ASSOCIATIVE LEARNING | 40 | -0.19 | -0.66 | 0.902 | 0.956 | 1.000 | 1704 | tags=10%, list=3%, signal=10% | |
4849 | REGULATION OF BEHAVIOR | 300 | -0.16 | -0.66 | 0.944 | 0.956 | 1.000 | 17769 | tags=29%, list=32%, signal=43% | |
4850 | DOPAMINE METABOLIC PROCESS | 27 | -0.21 | -0.66 | 0.899 | 0.956 | 1.000 | 36946 | tags=70%, list=68%, signal=217% | |
4851 | PLATELET-DERIVED GROWTH FACTOR RECEPTOR-BETA SIGNALING PATHWAY | 19 | -0.20 | -0.66 | 0.896 | 0.956 | 1.000 | 24797 | tags=47%, list=45%, signal=87% | |
4852 | CYTOLYSIS | 9 | -0.25 | -0.66 | 0.914 | 0.957 | 1.000 | 36677 | tags=78%, list=67%, signal=236% | |
4853 | ANGIOTENSIN-ACTIVATED SIGNALING PATHWAY | 28 | -0.21 | -0.65 | 0.880 | 0.958 | 1.000 | 16159 | tags=29%, list=30%, signal=41% | |
4854 | DNA REPLICATION CHECKPOINT | 21 | -0.22 | -0.65 | 0.908 | 0.958 | 1.000 | 30753 | tags=62%, list=56%, signal=141% | |
4855 | POSITIVE REGULATION OF FIBROBLAST PROLIFERATION | 66 | -0.18 | -0.65 | 0.945 | 0.958 | 1.000 | 34534 | tags=62%, list=63%, signal=168% | |
4856 | RETINA LAYER FORMATION | 35 | -0.19 | -0.65 | 0.888 | 0.958 | 1.000 | 33971 | tags=63%, list=62%, signal=166% | |
4857 | CELL-CELL RECOGNITION | 59 | -0.19 | -0.65 | 0.863 | 0.959 | 1.000 | 37214 | tags=66%, list=68%, signal=207% | |
4858 | URONIC ACID METABOLIC PROCESS | 34 | -0.20 | -0.65 | 0.897 | 0.959 | 1.000 | 35050 | tags=71%, list=64%, signal=197% | |
4859 | GLUCURONATE METABOLIC PROCESS | 34 | -0.20 | -0.65 | 0.897 | 0.959 | 1.000 | 35050 | tags=71%, list=64%, signal=197% | |
4860 | POSITIVE REGULATION OF INTEGRIN ACTIVATION | 14 | -0.25 | -0.65 | 0.881 | 0.958 | 1.000 | 21318 | tags=36%, list=39%, signal=59% | |
4861 | REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 64 | -0.19 | -0.65 | 0.947 | 0.959 | 1.000 | 29931 | tags=53%, list=55%, signal=117% | |
4862 | POSITIVE REGULATION OF FAT CELL DIFFERENTIATION | 65 | -0.18 | -0.65 | 0.941 | 0.959 | 1.000 | 40186 | tags=82%, list=73%, signal=307% | |
4863 | NEGATIVE REGULATION OF STRIATED MUSCLE TISSUE DEVELOPMENT | 35 | -0.19 | -0.65 | 0.905 | 0.959 | 1.000 | 25734 | tags=43%, list=47%, signal=81% | |
4864 | REGULATION OF CHEMOTAXIS | 250 | -0.17 | -0.65 | 0.936 | 0.959 | 1.000 | 13280 | tags=23%, list=24%, signal=31% | |
4865 | DERMATAN SULFATE PROTEOGLYCAN BIOSYNTHETIC PROCESS | 41 | -0.20 | -0.65 | 0.852 | 0.959 | 1.000 | 37972 | tags=76%, list=69%, signal=247% | |
4866 | DEVELOPMENT OF PRIMARY SEXUAL CHARACTERISTICS | 113 | -0.17 | -0.65 | 0.969 | 0.959 | 1.000 | 36628 | tags=64%, list=67%, signal=193% | |
4867 | NEGATIVE REGULATION OF GLIAL CELL DIFFERENTIATION | 20 | -0.21 | -0.65 | 0.878 | 0.959 | 1.000 | 26501 | tags=45%, list=48%, signal=87% | |
4868 | MEIOSIS I | 67 | -0.17 | -0.65 | 0.954 | 0.959 | 1.000 | 10382 | tags=18%, list=19%, signal=22% | |
4869 | SPERM CHROMATIN CONDENSATION | 16 | -0.23 | -0.65 | 0.909 | 0.959 | 1.000 | 7786 | tags=19%, list=14%, signal=22% | |
4870 | HEART PROCESS | 115 | -0.15 | -0.65 | 0.915 | 0.959 | 1.000 | 25515 | tags=39%, list=47%, signal=73% | |
4871 | NEGATIVE REGULATION OF LEUKOCYTE ACTIVATION | 172 | -0.18 | -0.65 | 0.912 | 0.959 | 1.000 | 22598 | tags=38%, list=41%, signal=64% | |
4872 | ZINC ION HOMEOSTASIS | 31 | -0.21 | -0.65 | 0.933 | 0.959 | 1.000 | 36291 | tags=74%, list=66%, signal=221% | |
4873 | SEX DETERMINATION | 19 | -0.23 | -0.65 | 0.871 | 0.959 | 1.000 | 31201 | tags=53%, list=57%, signal=123% | |
4874 | NEGATIVE REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 24 | -0.22 | -0.65 | 0.910 | 0.959 | 1.000 | 7618 | tags=21%, list=14%, signal=24% | |
4875 | REGULATION OF HORMONE BIOSYNTHETIC PROCESS | 28 | -0.21 | -0.65 | 0.920 | 0.960 | 1.000 | 21312 | tags=39%, list=39%, signal=64% | |
4876 | REGULATION OF KETONE BIOSYNTHETIC PROCESS | 22 | -0.21 | -0.65 | 0.904 | 0.959 | 1.000 | 37114 | tags=68%, list=68%, signal=212% | |
4877 | NEGATIVE REGULATION OF EPIDERMIS DEVELOPMENT | 14 | -0.22 | -0.65 | 0.924 | 0.959 | 1.000 | 33583 | tags=71%, list=61%, signal=185% | |
4878 | REGULATION OF STRIATED MUSCLE CELL DIFFERENTIATION | 132 | -0.18 | -0.65 | 0.881 | 0.959 | 1.000 | 9548 | tags=19%, list=17%, signal=23% | |
4879 | NEGATIVE REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 21 | -0.23 | -0.65 | 0.850 | 0.959 | 1.000 | 21623 | tags=38%, list=40%, signal=63% | |
4880 | NEGATIVE REGULATION OF ATP METABOLIC PROCESS | 21 | -0.23 | -0.65 | 0.850 | 0.959 | 1.000 | 21623 | tags=38%, list=40%, signal=63% | |
4881 | RESPONSE TO ELECTRICAL STIMULUS | 8 | -0.27 | -0.65 | 0.858 | 0.959 | 1.000 | 7817 | tags=25%, list=14%, signal=29% | |
4882 | FEMALE PREGNANCY | 110 | -0.17 | -0.65 | 0.925 | 0.959 | 1.000 | 19551 | tags=31%, list=36%, signal=48% | |
4883 | NEGATIVE REGULATION OF MUSCLE TISSUE DEVELOPMENT | 37 | -0.19 | -0.65 | 0.904 | 0.959 | 1.000 | 25734 | tags=43%, list=47%, signal=82% | |
4884 | MONOTERPENOID METABOLIC PROCESS | 22 | -0.22 | -0.65 | 0.892 | 0.959 | 1.000 | 33525 | tags=64%, list=61%, signal=164% | |
4885 | SENSORY ORGAN MORPHOGENESIS | 208 | -0.15 | -0.65 | 0.983 | 0.960 | 1.000 | 30361 | tags=50%, list=56%, signal=111% | |
4886 | POSITIVE REGULATION OF EMBRYONIC DEVELOPMENT | 68 | -0.17 | -0.65 | 0.964 | 0.960 | 1.000 | 33383 | tags=56%, list=61%, signal=143% | |
4887 | ACID SECRETION | 88 | -0.17 | -0.65 | 0.957 | 0.960 | 1.000 | 17082 | tags=30%, list=31%, signal=43% | |
4888 | GRANULOCYTE MIGRATION | 63 | -0.21 | -0.65 | 0.871 | 0.960 | 1.000 | 17066 | tags=29%, list=31%, signal=41% | |
4889 | POSITIVE REGULATION OF CATENIN IMPORT INTO NUCLEUS | 26 | -0.21 | -0.65 | 0.857 | 0.960 | 1.000 | 30999 | tags=58%, list=57%, signal=133% | |
4890 | OPIOID RECEPTOR SIGNALING PATHWAY | 10 | -0.26 | -0.65 | 0.910 | 0.961 | 1.000 | 32950 | tags=50%, list=60%, signal=126% | |
4891 | REGULATION OF HAIR FOLLICLE DEVELOPMENT | 13 | -0.25 | -0.65 | 0.875 | 0.961 | 1.000 | 23594 | tags=46%, list=43%, signal=81% | |
4892 | POSITIVE REGULATION OF CATION TRANSMEMBRANE TRANSPORT | 159 | -0.15 | -0.65 | 0.980 | 0.961 | 1.000 | 20983 | tags=35%, list=38%, signal=57% | |
4893 | REGULATION OF BONE MINERALIZATION | 109 | -0.17 | -0.65 | 0.983 | 0.961 | 1.000 | 30361 | tags=51%, list=56%, signal=115% | |
4894 | NEGATIVE REGULATION OF EPITHELIAL CELL MIGRATION | 132 | -0.16 | -0.65 | 0.967 | 0.961 | 1.000 | 37026 | tags=66%, list=68%, signal=204% | |
4895 | NEGATIVE REGULATION OF CD4-POSITIVE, ALPHA-BETA T CELL ACTIVATION | 25 | -0.21 | -0.65 | 0.891 | 0.961 | 1.000 | 30991 | tags=56%, list=57%, signal=129% | |
4896 | BASIC AMINO ACID TRANSMEMBRANE TRANSPORT | 11 | -0.26 | -0.65 | 0.885 | 0.961 | 1.000 | 7512 | tags=18%, list=14%, signal=21% | |
4897 | EYE DEVELOPMENT | 307 | -0.15 | -0.65 | 0.998 | 0.961 | 1.000 | 34300 | tags=57%, list=63%, signal=153% | |
4898 | CHONDROCYTE DIFFERENTIATION | 71 | -0.18 | -0.65 | 0.945 | 0.961 | 1.000 | 36193 | tags=69%, list=66%, signal=204% | |
4899 | CELL RECOGNITION | 141 | -0.18 | -0.65 | 0.895 | 0.961 | 1.000 | 37214 | tags=65%, list=68%, signal=204% | |
4900 | FIBRIL ORGANIZATION | 46 | -0.19 | -0.65 | 0.929 | 0.962 | 1.000 | 30049 | tags=57%, list=55%, signal=125% | |
4901 | NEGATIVE REGULATION OF EPIDERMAL CELL DIFFERENTIATION | 13 | -0.22 | -0.64 | 0.915 | 0.962 | 1.000 | 33180 | tags=69%, list=61%, signal=176% | |
4902 | REGULATION OF PHOSPHOLIPID BIOSYNTHETIC PROCESS | 19 | -0.21 | -0.64 | 0.922 | 0.961 | 1.000 | 31126 | tags=63%, list=57%, signal=147% | |
4903 | POSITIVE REGULATION OF DNA DAMAGE RESPONSE, SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 32 | -0.21 | -0.64 | 0.886 | 0.961 | 1.000 | 34726 | tags=66%, list=64%, signal=180% | |
4904 | ETHER LIPID BIOSYNTHETIC PROCESS | 13 | -0.27 | -0.64 | 0.834 | 0.961 | 1.000 | 39801 | tags=100%, list=73%, signal=368% | |
4905 | GLYCEROL ETHER BIOSYNTHETIC PROCESS | 13 | -0.27 | -0.64 | 0.834 | 0.961 | 1.000 | 39801 | tags=100%, list=73%, signal=368% | |
4906 | CELLULAR LIPID BIOSYNTHETIC PROCESS | 13 | -0.27 | -0.64 | 0.834 | 0.961 | 1.000 | 39801 | tags=100%, list=73%, signal=368% | |
4907 | ETHER BIOSYNTHETIC PROCESS | 13 | -0.27 | -0.64 | 0.834 | 0.961 | 1.000 | 39801 | tags=100%, list=73%, signal=368% | |
4908 | NEGATIVE REGULATION OF I-KAPPAB KINASE/NF-KAPPAB SIGNALING | 115 | -0.17 | -0.64 | 0.959 | 0.961 | 1.000 | 37233 | tags=67%, list=68%, signal=209% | |
4909 | CARDIAC MUSCLE CELL ACTION POTENTIAL | 61 | -0.16 | -0.64 | 0.963 | 0.961 | 1.000 | 25515 | tags=39%, list=47%, signal=74% | |
4910 | POSITIVE REGULATION OF SYNAPSE MATURATION | 19 | -0.23 | -0.64 | 0.858 | 0.961 | 1.000 | 1161 | tags=11%, list=2%, signal=11% | |
4911 | EXTRACELLULAR MATRIX ORGANIZATION | 769 | -0.15 | -0.64 | 0.938 | 0.961 | 1.000 | 37840 | tags=65%, list=69%, signal=209% | |
4912 | NEGATIVE REGULATION OF SECRETION | 224 | -0.16 | -0.64 | 0.968 | 0.962 | 1.000 | 37114 | tags=64%, list=68%, signal=198% | |
4913 | REGULATION OF SYSTEM PROCESS | 687 | -0.14 | -0.64 | 0.965 | 0.963 | 1.000 | 23432 | tags=35%, list=43%, signal=61% | |
4914 | BLOOD COAGULATION, INTRINSIC PATHWAY | 33 | -0.20 | -0.64 | 0.896 | 0.963 | 1.000 | 18320 | tags=33%, list=34%, signal=50% | |
4915 | EXTRACELLULAR STRUCTURE ORGANIZATION | 770 | -0.15 | -0.64 | 0.934 | 0.962 | 1.000 | 37840 | tags=65%, list=69%, signal=208% | |
4916 | FOREBRAIN NEURON DIFFERENTIATION | 49 | -0.18 | -0.64 | 0.935 | 0.962 | 1.000 | 38997 | tags=76%, list=71%, signal=263% | |
4917 | NEGATIVE REGULATION OF CELL KILLING | 27 | -0.26 | -0.64 | 0.876 | 0.963 | 1.000 | 13927 | tags=33%, list=25%, signal=45% | |
4918 | REGULATION OF ANTIGEN RECEPTOR-MEDIATED SIGNALING PATHWAY | 72 | -0.20 | -0.64 | 0.876 | 0.963 | 1.000 | 13664 | tags=26%, list=25%, signal=35% | |
4919 | INNATE IMMUNE RESPONSE IN MUCOSA | 20 | -0.22 | -0.64 | 0.851 | 0.963 | 1.000 | 30530 | tags=65%, list=56%, signal=147% | |
4920 | MALE SEX DIFFERENTIATION | 79 | -0.17 | -0.64 | 0.903 | 0.963 | 1.000 | 36786 | tags=66%, list=67%, signal=201% | |
4921 | REGULATION OF HUMORAL IMMUNE RESPONSE MEDIATED BY CIRCULATING IMMUNOGLOBULIN | 12 | -0.27 | -0.64 | 0.901 | 0.963 | 1.000 | 9310 | tags=25%, list=17%, signal=30% | |
4922 | NEGATIVE REGULATION OF HUMORAL IMMUNE RESPONSE MEDIATED BY CIRCULATING IMMUNOGLOBULIN | 12 | -0.27 | -0.64 | 0.901 | 0.963 | 1.000 | 9310 | tags=25%, list=17%, signal=30% | |
4923 | CYTIDINE CATABOLIC PROCESS | 12 | -0.26 | -0.64 | 0.890 | 0.963 | 1.000 | 2095 | tags=17%, list=4%, signal=17% | |
4924 | CYTIDINE DEAMINATION | 12 | -0.26 | -0.64 | 0.890 | 0.963 | 1.000 | 2095 | tags=17%, list=4%, signal=17% | |
4925 | CYTIDINE METABOLIC PROCESS | 12 | -0.26 | -0.64 | 0.890 | 0.962 | 1.000 | 2095 | tags=17%, list=4%, signal=17% | |
4926 | BLEB ASSEMBLY | 18 | -0.25 | -0.64 | 0.865 | 0.962 | 1.000 | 32664 | tags=72%, list=60%, signal=179% | |
4927 | ADAPTIVE IMMUNE RESPONSE | 232 | -0.16 | -0.64 | 0.922 | 0.963 | 1.000 | 27979 | tags=44%, list=51%, signal=91% | |
4928 | NEGATIVE REGULATION OF KERATINOCYTE DIFFERENTIATION | 10 | -0.24 | -0.64 | 0.895 | 0.963 | 1.000 | 33180 | tags=70%, list=61%, signal=178% | |
4929 | SUPEROXIDE METABOLIC PROCESS | 44 | -0.21 | -0.64 | 0.870 | 0.964 | 1.000 | 9198 | tags=23%, list=17%, signal=27% | |
4930 | REGULATION OF ION TRANSPORT | 865 | -0.14 | -0.64 | 0.977 | 0.964 | 1.000 | 21623 | tags=33%, list=40%, signal=54% | |
4931 | RESPONSE TO FUNGUS | 30 | -0.22 | -0.64 | 0.892 | 0.964 | 1.000 | 17066 | tags=30%, list=31%, signal=44% | |
4932 | REGULATION OF CYCLASE ACTIVITY | 130 | -0.16 | -0.64 | 0.954 | 0.964 | 1.000 | 28908 | tags=44%, list=53%, signal=93% | |
4933 | RESPONSE TO TUMOR CELL | 9 | -0.25 | -0.64 | 0.902 | 0.964 | 1.000 | 36897 | tags=89%, list=67%, signal=273% | |
4934 | POSITIVE REGULATION OF MITOCHONDRIAL DEPOLARIZATION | 11 | -0.27 | -0.64 | 0.872 | 0.964 | 1.000 | 37026 | tags=91%, list=68%, signal=282% | |
4935 | POSITIVE REGULATION OF GASTRULATION | 10 | -0.25 | -0.64 | 0.897 | 0.964 | 1.000 | 19273 | tags=40%, list=35%, signal=62% | |
4936 | ALDITOL METABOLIC PROCESS | 18 | -0.22 | -0.64 | 0.901 | 0.964 | 1.000 | 5653 | tags=17%, list=10%, signal=19% | |
4937 | INNER DYNEIN ARM ASSEMBLY | 30 | -0.22 | -0.64 | 0.826 | 0.965 | 1.000 | 34039 | tags=70%, list=62%, signal=185% | |
4938 | LUNG ALVEOLUS DEVELOPMENT | 29 | -0.19 | -0.64 | 0.884 | 0.965 | 1.000 | 33770 | tags=59%, list=62%, signal=153% | |
4939 | STRIATED MUSCLE TISSUE DEVELOPMENT | 249 | -0.14 | -0.64 | 0.998 | 0.965 | 1.000 | 32149 | tags=54%, list=59%, signal=130% | |
4940 | CYCLOOXYGENASE PATHWAY | 28 | -0.21 | -0.64 | 0.903 | 0.965 | 1.000 | 39148 | tags=82%, list=72%, signal=289% | |
4941 | NEGATIVE REGULATION OF ACTIVIN RECEPTOR SIGNALING PATHWAY | 14 | -0.22 | -0.64 | 0.929 | 0.965 | 1.000 | 28190 | tags=50%, list=52%, signal=103% | |
4942 | T CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 63 | -0.20 | -0.64 | 0.921 | 0.965 | 1.000 | 37233 | tags=73%, list=68%, signal=229% | |
4943 | REGULATION OF RELAXATION OF MUSCLE | 18 | -0.23 | -0.64 | 0.909 | 0.965 | 1.000 | 28323 | tags=56%, list=52%, signal=115% | |
4944 | REGULATION OF VASCULAR PERMEABILITY | 45 | -0.18 | -0.64 | 0.924 | 0.965 | 1.000 | 9919 | tags=18%, list=18%, signal=22% | |
4945 | REGULATION OF MAST CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 32 | -0.20 | -0.64 | 0.884 | 0.965 | 1.000 | 9282 | tags=19%, list=17%, signal=23% | |
4946 | RESPONSE TO CADMIUM ION | 13 | -0.27 | -0.64 | 0.865 | 0.965 | 1.000 | 28246 | tags=62%, list=52%, signal=127% | |
4947 | C21-STEROID HORMONE METABOLIC PROCESS | 35 | -0.18 | -0.64 | 0.892 | 0.965 | 1.000 | 33208 | tags=60%, list=61%, signal=153% | |
4948 | ANGIOGENESIS | 303 | -0.15 | -0.64 | 0.989 | 0.965 | 1.000 | 35777 | tags=62%, list=65%, signal=179% | |
4949 | POSITIVE REGULATION OF MUSCLE CELL DIFFERENTIATION | 171 | -0.16 | -0.64 | 0.933 | 0.965 | 1.000 | 35905 | tags=63%, list=66%, signal=183% | |
4950 | REGULATION OF CELL KILLING | 94 | -0.19 | -0.64 | 0.921 | 0.964 | 1.000 | 17332 | tags=31%, list=32%, signal=45% | |
4951 | POSITIVE REGULATION OF CAMP BIOSYNTHETIC PROCESS | 126 | -0.16 | -0.64 | 0.936 | 0.964 | 1.000 | 30167 | tags=46%, list=55%, signal=102% | |
4952 | DENDRITIC SPINE MORPHOGENESIS | 28 | -0.19 | -0.64 | 0.906 | 0.964 | 1.000 | 29821 | tags=57%, list=55%, signal=126% | |
4953 | NEGATIVE REGULATION OF CELL ACTIVATION | 201 | -0.17 | -0.64 | 0.936 | 0.964 | 1.000 | 33167 | tags=57%, list=61%, signal=144% | |
4954 | MYELOID DENDRITIC CELL ACTIVATION | 27 | -0.20 | -0.64 | 0.928 | 0.964 | 1.000 | 24249 | tags=41%, list=44%, signal=73% | |
4955 | REGULATION OF OSSIFICATION | 234 | -0.16 | -0.64 | 0.990 | 0.964 | 1.000 | 30878 | tags=50%, list=56%, signal=115% | |
4956 | POSITIVE REGULATION OF LIPID STORAGE | 42 | -0.21 | -0.64 | 0.893 | 0.964 | 1.000 | 38685 | tags=79%, list=71%, signal=268% | |
4957 | NEGATIVE REGULATION OF INSULIN-LIKE GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 14 | -0.24 | -0.63 | 0.892 | 0.964 | 1.000 | 38679 | tags=79%, list=71%, signal=268% | |
4958 | POSITIVE REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 35 | -0.20 | -0.63 | 0.897 | 0.964 | 1.000 | 38520 | tags=74%, list=70%, signal=251% | |
4959 | REGULATION OF TISSUE REMODELING | 77 | -0.17 | -0.63 | 0.966 | 0.964 | 1.000 | 38257 | tags=71%, list=70%, signal=238% | |
4960 | REGULATION OF MACROPHAGE DIFFERENTIATION | 34 | -0.19 | -0.63 | 0.948 | 0.964 | 1.000 | 8905 | tags=18%, list=16%, signal=21% | |
4961 | ANTERIOR/POSTERIOR AXIS SPECIFICATION | 35 | -0.22 | -0.63 | 0.856 | 0.964 | 1.000 | 11428 | tags=23%, list=21%, signal=29% | |
4962 | ENDOCARDIAL CUSHION MORPHOGENESIS | 25 | -0.20 | -0.63 | 0.924 | 0.964 | 1.000 | 27150 | tags=48%, list=50%, signal=95% | |
4963 | POSITIVE REGULATION OF URINE VOLUME | 17 | -0.22 | -0.63 | 0.885 | 0.964 | 1.000 | 39043 | tags=76%, list=71%, signal=267% | |
4964 | NERVE GROWTH FACTOR SIGNALING PATHWAY | 24 | -0.22 | -0.63 | 0.896 | 0.964 | 1.000 | 19702 | tags=38%, list=36%, signal=59% | |
4965 | NEGATIVE REGULATION OF CELL AGING | 31 | -0.20 | -0.63 | 0.890 | 0.965 | 1.000 | 34776 | tags=68%, list=64%, signal=186% | |
4966 | CHYLOMICRON REMNANT CLEARANCE | 12 | -0.28 | -0.63 | 0.849 | 0.965 | 1.000 | 19183 | tags=42%, list=35%, signal=64% | |
4967 | TRIGLYCERIDE-RICH LIPOPROTEIN PARTICLE CLEARANCE | 12 | -0.28 | -0.63 | 0.849 | 0.964 | 1.000 | 19183 | tags=42%, list=35%, signal=64% | |
4968 | RESPONSE TO BACTERIAL LIPOPEPTIDE | 14 | -0.27 | -0.63 | 0.873 | 0.964 | 1.000 | 31155 | tags=71%, list=57%, signal=166% | |
4969 | CELLULAR RESPONSE TO BACTERIAL LIPOPROTEIN | 14 | -0.27 | -0.63 | 0.873 | 0.964 | 1.000 | 31155 | tags=71%, list=57%, signal=166% | |
4970 | CELLULAR RESPONSE TO BACTERIAL LIPOPEPTIDE | 14 | -0.27 | -0.63 | 0.873 | 0.964 | 1.000 | 31155 | tags=71%, list=57%, signal=166% | |
4971 | POSITIVE REGULATION OF INTERLEUKIN-2 PRODUCTION | 61 | -0.19 | -0.63 | 0.936 | 0.964 | 1.000 | 30313 | tags=51%, list=55%, signal=114% | |
4972 | INORGANIC ANION TRANSMEMBRANE TRANSPORT | 146 | -0.16 | -0.63 | 0.954 | 0.964 | 1.000 | 24828 | tags=40%, list=45%, signal=73% | |
4973 | HEART TRABECULA FORMATION | 13 | -0.22 | -0.63 | 0.893 | 0.964 | 1.000 | 25055 | tags=54%, list=46%, signal=99% | |
4974 | NEGATIVE REGULATION OF HYDROGEN PEROXIDE-INDUCED CELL DEATH | 30 | -0.19 | -0.63 | 0.973 | 0.964 | 1.000 | 9001 | tags=20%, list=16%, signal=24% | |
4975 | SEQUESTERING OF ACTIN MONOMERS | 16 | -0.22 | -0.63 | 0.918 | 0.964 | 1.000 | 1997 | tags=13%, list=4%, signal=13% | |
4976 | ADENYLATE CYCLASE-MODULATING G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 172 | -0.16 | -0.63 | 0.948 | 0.963 | 1.000 | 20717 | tags=31%, list=38%, signal=49% | |
4977 | NEGATIVE REGULATION OF FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 18 | -0.23 | -0.63 | 0.861 | 0.964 | 1.000 | 36858 | tags=83%, list=67%, signal=256% | |
4978 | WNT SIGNALING PATHWAY INVOLVED IN MIDBRAIN DOPAMINERGIC NEURON DIFFERENTIATION | 9 | -0.28 | -0.63 | 0.859 | 0.964 | 1.000 | 34770 | tags=78%, list=64%, signal=214% | |
4979 | REGULATION OF NOREPINEPHRINE SECRETION | 7 | -0.26 | -0.63 | 0.917 | 0.963 | 1.000 | 2684 | tags=14%, list=5%, signal=15% | |
4980 | NEGATIVE REGULATION OF ENDOTHELIAL CELL MIGRATION | 104 | -0.16 | -0.63 | 0.964 | 0.963 | 1.000 | 19583 | tags=33%, list=36%, signal=51% | |
4981 | SODIUM-DEPENDENT PHOSPHATE TRANSPORT | 8 | -0.28 | -0.63 | 0.903 | 0.963 | 1.000 | 24052 | tags=38%, list=44%, signal=67% | |
4982 | RELEASE OF SEQUESTERED CALCIUM ION INTO CYTOSOL | 74 | -0.18 | -0.63 | 0.910 | 0.963 | 1.000 | 32656 | tags=58%, list=60%, signal=144% | |
4983 | NEGATIVE REGULATION OF SEQUESTERING OF CALCIUM ION | 74 | -0.18 | -0.63 | 0.910 | 0.963 | 1.000 | 32656 | tags=58%, list=60%, signal=144% | |
4984 | CALCIUM ION TRANSMEMBRANE IMPORT INTO CYTOSOL | 74 | -0.18 | -0.63 | 0.910 | 0.963 | 1.000 | 32656 | tags=58%, list=60%, signal=144% | |
4985 | CALCIUM ION IMPORT INTO CYTOSOL | 74 | -0.18 | -0.63 | 0.910 | 0.962 | 1.000 | 32656 | tags=58%, list=60%, signal=144% | |
4986 | CONNECTIVE TISSUE DEVELOPMENT | 168 | -0.15 | -0.63 | 0.979 | 0.962 | 1.000 | 20764 | tags=33%, list=38%, signal=54% | |
4987 | NEGATIVE REGULATION OF ENDOTHELIAL CELL APOPTOTIC PROCESS | 47 | -0.20 | -0.63 | 0.924 | 0.962 | 1.000 | 30969 | tags=55%, list=57%, signal=127% | |
4988 | BONE MATURATION | 28 | -0.20 | -0.63 | 0.938 | 0.962 | 1.000 | 20764 | tags=29%, list=38%, signal=46% | |
4989 | CELL-CELL ADHESION VIA PLASMA-MEMBRANE ADHESION MOLECULES | 175 | -0.15 | -0.63 | 0.983 | 0.963 | 1.000 | 37241 | tags=65%, list=68%, signal=204% | |
4990 | NEGATIVE REGULATION OF CREB TRANSCRIPTION FACTOR ACTIVITY | 8 | -0.28 | -0.63 | 0.891 | 0.963 | 1.000 | 11428 | tags=25%, list=21%, signal=32% | |
4991 | PRESYNAPTIC MEMBRANE ASSEMBLY | 31 | -0.20 | -0.63 | 0.896 | 0.963 | 1.000 | 18558 | tags=35%, list=34%, signal=54% | |
4992 | SEGMENTATION | 38 | -0.18 | -0.63 | 0.918 | 0.963 | 1.000 | 15207 | tags=24%, list=28%, signal=33% | |
4993 | REGULATION OF PURINE NUCLEOTIDE METABOLIC PROCESS | 300 | -0.15 | -0.63 | 0.980 | 0.962 | 1.000 | 30255 | tags=47%, list=55%, signal=105% | |
4994 | CAMERA-TYPE EYE DEVELOPMENT | 209 | -0.14 | -0.63 | 0.989 | 0.962 | 1.000 | 36275 | tags=62%, list=66%, signal=183% | |
4995 | SODIUM ION TRANSMEMBRANE TRANSPORT | 163 | -0.15 | -0.63 | 0.971 | 0.962 | 1.000 | 24633 | tags=37%, list=45%, signal=68% | |
4996 | RESPONSE TO EPINEPHRINE | 28 | -0.21 | -0.63 | 0.932 | 0.962 | 1.000 | 28323 | tags=50%, list=52%, signal=104% | |
4997 | CELLULAR RESPONSE TO EPINEPHRINE STIMULUS | 28 | -0.21 | -0.63 | 0.932 | 0.962 | 1.000 | 28323 | tags=50%, list=52%, signal=104% | |
4998 | POSITIVE REGULATION OF PROTEIN KINASE C SIGNALING | 19 | -0.21 | -0.63 | 0.926 | 0.963 | 1.000 | 35029 | tags=68%, list=64%, signal=190% | |
4999 | TRABECULA FORMATION | 16 | -0.21 | -0.63 | 0.897 | 0.963 | 1.000 | 32496 | tags=69%, list=59%, signal=169% | |
5000 | POSITIVE REGULATION OF CHOLESTEROL STORAGE | 21 | -0.26 | -0.63 | 0.884 | 0.963 | 1.000 | 2398 | tags=14%, list=4%, signal=15% | |
5001 | SPINAL CORD DEVELOPMENT | 59 | -0.17 | -0.63 | 0.923 | 0.963 | 1.000 | 34353 | tags=63%, list=63%, signal=169% | |
5002 | INDOLALKYLAMINE METABOLIC PROCESS | 30 | -0.20 | -0.63 | 0.909 | 0.963 | 1.000 | 33770 | tags=60%, list=62%, signal=157% | |
5003 | CALCIUM ION TRANSMEMBRANE TRANSPORT | 285 | -0.14 | -0.63 | 0.954 | 0.963 | 1.000 | 29350 | tags=44%, list=54%, signal=94% | |
5004 | CARTILAGE DEVELOPMENT | 133 | -0.16 | -0.63 | 0.975 | 0.964 | 1.000 | 35838 | tags=61%, list=66%, signal=176% | |
5005 | CELLULAR RESPONSE TO MOLECULE OF BACTERIAL ORIGIN | 156 | -0.20 | -0.63 | 0.893 | 0.964 | 1.000 | 7557 | tags=17%, list=14%, signal=20% | |
5006 | DETECTION OF CALCIUM ION | 41 | -0.19 | -0.63 | 0.911 | 0.964 | 1.000 | 22210 | tags=37%, list=41%, signal=62% | |
5007 | NEGATIVE REGULATION OF SECRETION BY CELL | 200 | -0.16 | -0.63 | 0.950 | 0.964 | 1.000 | 37114 | tags=64%, list=68%, signal=197% | |
5008 | POSITIVE REGULATION OF ANTIGEN RECEPTOR-MEDIATED SIGNALING PATHWAY | 25 | -0.24 | -0.63 | 0.896 | 0.964 | 1.000 | 8390 | tags=20%, list=15%, signal=24% | |
5009 | EXTRACELLULAR MATRIX DISASSEMBLY | 307 | -0.15 | -0.63 | 0.903 | 0.965 | 1.000 | 37791 | tags=65%, list=69%, signal=209% | |
5010 | NEGATIVE REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 15 | -0.22 | -0.63 | 0.909 | 0.964 | 1.000 | 24797 | tags=47%, list=45%, signal=85% | |
5011 | HEART VALVE FORMATION | 15 | -0.23 | -0.63 | 0.924 | 0.965 | 1.000 | 5907 | tags=13%, list=11%, signal=15% | |
5012 | S-ADENOSYLMETHIONINE METABOLIC PROCESS | 10 | -0.25 | -0.63 | 0.901 | 0.964 | 1.000 | 18327 | tags=40%, list=34%, signal=60% | |
5013 | POSITIVE REGULATION OF ANGIOGENESIS | 206 | -0.16 | -0.63 | 0.968 | 0.964 | 1.000 | 35356 | tags=59%, list=65%, signal=167% | |
5014 | NEGATIVE REGULATION OF STEROID BIOSYNTHETIC PROCESS | 35 | -0.19 | -0.63 | 0.936 | 0.964 | 1.000 | 37114 | tags=69%, list=68%, signal=213% | |
5015 | NEGATIVE REGULATION OF STEROID METABOLIC PROCESS | 35 | -0.19 | -0.63 | 0.936 | 0.964 | 1.000 | 37114 | tags=69%, list=68%, signal=213% | |
5016 | NEGATIVE REGULATION OF EMBRYONIC DEVELOPMENT | 43 | -0.17 | -0.63 | 0.930 | 0.965 | 1.000 | 39370 | tags=74%, list=72%, signal=266% | |
5017 | ENDOSOME TRANSPORT VIA MULTIVESICULAR BODY SORTING PATHWAY | 10 | -0.25 | -0.63 | 0.909 | 0.965 | 1.000 | 37727 | tags=90%, list=69%, signal=290% | |
5018 | METANEPHROS MORPHOGENESIS | 29 | -0.20 | -0.62 | 0.899 | 0.966 | 1.000 | 32287 | tags=59%, list=59%, signal=143% | |
5019 | REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 108 | -0.17 | -0.62 | 0.981 | 0.966 | 1.000 | 41233 | tags=81%, list=75%, signal=331% | |
5020 | REGULATION OF MONOCYTE CHEMOTAXIS | 40 | -0.20 | -0.62 | 0.914 | 0.966 | 1.000 | 27777 | tags=52%, list=51%, signal=107% | |
5021 | POSITIVE REGULATION OF SODIUM ION TRANSPORT | 56 | -0.16 | -0.62 | 0.971 | 0.966 | 1.000 | 25853 | tags=46%, list=47%, signal=88% | |
5022 | CENTRAL NERVOUS SYSTEM PROJECTION NEURON AXONOGENESIS | 39 | -0.18 | -0.62 | 0.922 | 0.966 | 1.000 | 21164 | tags=36%, list=39%, signal=59% | |
5023 | COLUMNAR/CUBOIDAL EPITHELIAL CELL DIFFERENTIATION | 81 | -0.16 | -0.62 | 0.931 | 0.966 | 1.000 | 33117 | tags=54%, list=61%, signal=138% | |
5024 | REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 65 | -0.18 | -0.62 | 0.922 | 0.966 | 1.000 | 36090 | tags=63%, list=66%, signal=185% | |
5025 | REGULATION OF B CELL DIFFERENTIATION | 23 | -0.21 | -0.62 | 0.872 | 0.967 | 1.000 | 4505 | tags=13%, list=8%, signal=14% | |
5026 | MUSCLE TISSUE DEVELOPMENT | 270 | -0.14 | -0.62 | 0.996 | 0.967 | 1.000 | 32664 | tags=54%, list=60%, signal=135% | |
5027 | REGULATION OF NEUROTRANSMITTER LEVELS | 258 | -0.14 | -0.62 | 0.990 | 0.967 | 1.000 | 17082 | tags=28%, list=31%, signal=40% | |
5028 | INFLAMMATORY RESPONSE TO ANTIGENIC STIMULUS | 22 | -0.21 | -0.62 | 0.896 | 0.966 | 1.000 | 24586 | tags=45%, list=45%, signal=83% | |
5029 | LUNG MORPHOGENESIS | 23 | -0.20 | -0.62 | 0.906 | 0.966 | 1.000 | 33089 | tags=57%, list=61%, signal=143% | |
5030 | SENSORY PERCEPTION | 444 | -0.14 | -0.62 | 0.970 | 0.967 | 1.000 | 24433 | tags=37%, list=45%, signal=66% | |
5031 | NEGATIVE REGULATION OF HUMORAL IMMUNE RESPONSE | 23 | -0.23 | -0.62 | 0.874 | 0.967 | 1.000 | 23098 | tags=48%, list=42%, signal=83% | |
5032 | POSITIVE REGULATION OF MITOTIC NUCLEAR DIVISION | 91 | -0.17 | -0.62 | 0.938 | 0.967 | 1.000 | 30219 | tags=54%, list=55%, signal=120% | |
5033 | BONE GROWTH | 22 | -0.21 | -0.62 | 0.893 | 0.967 | 1.000 | 35160 | tags=64%, list=64%, signal=178% | |
5034 | NEGATIVE REGULATION OF TRIGLYCERIDE METABOLIC PROCESS | 19 | -0.20 | -0.62 | 0.921 | 0.968 | 1.000 | 13967 | tags=26%, list=26%, signal=35% | |
5035 | NEGATIVE REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 33 | -0.18 | -0.62 | 0.910 | 0.968 | 1.000 | 20416 | tags=36%, list=37%, signal=58% | |
5036 | POSITIVE REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 75 | -0.17 | -0.62 | 0.973 | 0.968 | 1.000 | 30361 | tags=48%, list=56%, signal=108% | |
5037 | NEGATIVE REGULATION OF INTERLEUKIN-6 PRODUCTION | 53 | -0.21 | -0.62 | 0.894 | 0.968 | 1.000 | 23310 | tags=42%, list=43%, signal=72% | |
5038 | REGULATION OF GASTRULATION | 59 | -0.18 | -0.62 | 0.949 | 0.968 | 1.000 | 20021 | tags=36%, list=37%, signal=56% | |
5039 | REGULATION OF HETEROTYPIC CELL-CELL ADHESION | 52 | -0.22 | -0.62 | 0.882 | 0.969 | 1.000 | 20622 | tags=38%, list=38%, signal=62% | |
5040 | COLLECTING DUCT DEVELOPMENT | 13 | -0.24 | -0.62 | 0.922 | 0.969 | 1.000 | 14059 | tags=31%, list=26%, signal=41% | |
5041 | RESPONSE TO MACROPHAGE COLONY-STIMULATING FACTOR | 8 | -0.24 | -0.62 | 0.909 | 0.969 | 1.000 | 11376 | tags=25%, list=21%, signal=32% | |
5042 | CELLULAR RESPONSE TO MACROPHAGE COLONY-STIMULATING FACTOR STIMULUS | 8 | -0.24 | -0.62 | 0.909 | 0.969 | 1.000 | 11376 | tags=25%, list=21%, signal=32% | |
5043 | POSITIVE REGULATION OF SEQUESTERING OF TRIGLYCERIDE | 18 | -0.21 | -0.62 | 0.913 | 0.969 | 1.000 | 29616 | tags=56%, list=54%, signal=121% | |
5044 | EMBRYONIC HEMOPOIESIS | 27 | -0.19 | -0.62 | 0.931 | 0.970 | 1.000 | 31667 | tags=56%, list=58%, signal=132% | |
5045 | NEGATIVE REGULATION OF LIPID BIOSYNTHETIC PROCESS | 61 | -0.17 | -0.62 | 0.958 | 0.970 | 1.000 | 34824 | tags=62%, list=64%, signal=171% | |
5046 | POSITIVE REGULATION OF MONOCYTE CHEMOTAXIS | 28 | -0.21 | -0.62 | 0.916 | 0.969 | 1.000 | 27777 | tags=54%, list=51%, signal=109% | |
5047 | NEGATIVE REGULATION OF CYTOKINE BIOSYNTHETIC PROCESS | 37 | -0.19 | -0.62 | 0.889 | 0.969 | 1.000 | 22653 | tags=38%, list=41%, signal=65% | |
5048 | MIDDLE EAR MORPHOGENESIS | 9 | -0.25 | -0.62 | 0.925 | 0.970 | 1.000 | 12604 | tags=22%, list=23%, signal=29% | |
5049 | PANCREAS DEVELOPMENT | 97 | -0.15 | -0.62 | 0.966 | 0.970 | 1.000 | 21017 | tags=33%, list=38%, signal=53% | |
5050 | SMOOTH MUSCLE CELL DIFFERENTIATION | 33 | -0.19 | -0.62 | 0.907 | 0.970 | 1.000 | 28925 | tags=52%, list=53%, signal=109% | |
5051 | VENOUS BLOOD VESSEL DEVELOPMENT | 25 | -0.19 | -0.62 | 0.931 | 0.970 | 1.000 | 35838 | tags=68%, list=66%, signal=197% | |
5052 | POSITIVE REGULATION OF PURINE NUCLEOTIDE METABOLIC PROCESS | 191 | -0.15 | -0.62 | 0.970 | 0.970 | 1.000 | 30219 | tags=46%, list=55%, signal=103% | |
5053 | VASCULOGENESIS | 46 | -0.17 | -0.61 | 0.954 | 0.971 | 1.000 | 35345 | tags=65%, list=65%, signal=184% | |
5054 | POSITIVE REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS | 34 | -0.20 | -0.61 | 0.918 | 0.971 | 1.000 | 35225 | tags=62%, list=64%, signal=174% | |
5055 | CELLULAR EXTRAVASATION | 41 | -0.19 | -0.61 | 0.903 | 0.972 | 1.000 | 32679 | tags=66%, list=60%, signal=164% | |
5056 | LYMPH VESSEL MORPHOGENESIS | 34 | -0.18 | -0.61 | 0.943 | 0.972 | 1.000 | 36113 | tags=68%, list=66%, signal=199% | |
5057 | REGULATION OF DNA METHYLATION | 21 | -0.21 | -0.61 | 0.938 | 0.973 | 1.000 | 34997 | tags=67%, list=64%, signal=185% | |
5058 | HEMATOPOIETIC PROGENITOR CELL DIFFERENTIATION | 55 | -0.20 | -0.61 | 0.901 | 0.972 | 1.000 | 23594 | tags=40%, list=43%, signal=70% | |
5059 | REGULATION OF NEUROTRANSMITTER TRANSPORT | 82 | -0.15 | -0.61 | 0.973 | 0.972 | 1.000 | 17863 | tags=29%, list=33%, signal=43% | |
5060 | DENDRITIC CELL MIGRATION | 27 | -0.23 | -0.61 | 0.888 | 0.973 | 1.000 | 25252 | tags=48%, list=46%, signal=89% | |
5061 | SKIN DEVELOPMENT | 169 | -0.16 | -0.61 | 0.952 | 0.973 | 1.000 | 16754 | tags=28%, list=31%, signal=40% | |
5062 | REGULATION OF ACTIN FILAMENT-BASED MOVEMENT | 53 | -0.17 | -0.61 | 0.955 | 0.973 | 1.000 | 32056 | tags=51%, list=59%, signal=123% | |
5063 | SPROUTING ANGIOGENESIS | 97 | -0.15 | -0.61 | 0.962 | 0.973 | 1.000 | 36427 | tags=65%, list=67%, signal=194% | |
5064 | CAMERA-TYPE EYE PHOTORECEPTOR CELL DIFFERENTIATION | 19 | -0.21 | -0.61 | 0.931 | 0.973 | 1.000 | 11296 | tags=21%, list=21%, signal=27% | |
5065 | HOMOLOGOUS CHROMOSOME SEGREGATION | 21 | -0.19 | -0.61 | 0.918 | 0.973 | 1.000 | 5264 | tags=14%, list=10%, signal=16% | |
5066 | APPENDAGE DEVELOPMENT | 138 | -0.14 | -0.61 | 0.963 | 0.973 | 1.000 | 24557 | tags=38%, list=45%, signal=68% | |
5067 | LIMB DEVELOPMENT | 138 | -0.14 | -0.61 | 0.963 | 0.973 | 1.000 | 24557 | tags=38%, list=45%, signal=68% | |
5068 | PROTEIN-COFACTOR LINKAGE | 8 | -0.27 | -0.61 | 0.888 | 0.973 | 1.000 | 37177 | tags=88%, list=68%, signal=273% | |
5069 | POSITIVE REGULATION OF HELICASE ACTIVITY | 14 | -0.25 | -0.61 | 0.865 | 0.973 | 1.000 | 17563 | tags=43%, list=32%, signal=63% | |
5070 | NEGATIVE REGULATION OF ANION TRANSPORT | 51 | -0.17 | -0.61 | 0.951 | 0.974 | 1.000 | 36946 | tags=75%, list=68%, signal=230% | |
5071 | INTERLEUKIN-1 SECRETION | 24 | -0.23 | -0.61 | 0.876 | 0.974 | 1.000 | 41418 | tags=96%, list=76%, signal=395% | |
5072 | SECRETION BY TISSUE | 26 | -0.20 | -0.61 | 0.956 | 0.974 | 1.000 | 16765 | tags=31%, list=31%, signal=44% | |
5073 | REGULATION OF METAL ION TRANSPORT | 503 | -0.14 | -0.61 | 1.000 | 0.974 | 1.000 | 21471 | tags=33%, list=39%, signal=54% | |
5074 | REGULATION OF PLASMA LIPOPROTEIN PARTICLE LEVELS | 82 | -0.18 | -0.61 | 0.918 | 0.974 | 1.000 | 37034 | tags=67%, list=68%, signal=208% | |
5075 | MUSCLE ORGAN DEVELOPMENT | 270 | -0.14 | -0.61 | 0.980 | 0.973 | 1.000 | 21818 | tags=33%, list=40%, signal=55% | |
5076 | AV NODE CELL ACTION POTENTIAL | 3 | -0.35 | -0.61 | 0.936 | 0.973 | 1.000 | 24367 | tags=67%, list=45%, signal=120% | |
5077 | AV NODE CELL TO BUNDLE OF HIS CELL SIGNALING | 3 | -0.35 | -0.61 | 0.936 | 0.973 | 1.000 | 24367 | tags=67%, list=45%, signal=120% | |
5078 | CYTOKINE METABOLIC PROCESS | 16 | -0.22 | -0.61 | 0.923 | 0.974 | 1.000 | 33453 | tags=69%, list=61%, signal=177% | |
5079 | NEURON-NEURON SYNAPTIC TRANSMISSION | 37 | -0.21 | -0.61 | 0.870 | 0.974 | 1.000 | 19646 | tags=38%, list=36%, signal=59% | |
5080 | VENOUS BLOOD VESSEL MORPHOGENESIS | 15 | -0.21 | -0.61 | 0.912 | 0.974 | 1.000 | 35029 | tags=67%, list=64%, signal=185% | |
5081 | REGULATION OF POTASSIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 90 | -0.15 | -0.61 | 0.994 | 0.974 | 1.000 | 25853 | tags=42%, list=47%, signal=80% | |
5082 | LIPID TRANSLOCATION | 14 | -0.23 | -0.61 | 0.919 | 0.974 | 1.000 | 31236 | tags=64%, list=57%, signal=150% | |
5083 | PHOSPHOLIPID TRANSLOCATION | 14 | -0.23 | -0.61 | 0.919 | 0.973 | 1.000 | 31236 | tags=64%, list=57%, signal=150% | |
5084 | POSITIVE REGULATION OF CELLULAR AMINO ACID METABOLIC PROCESS | 16 | -0.23 | -0.61 | 0.922 | 0.973 | 1.000 | 32287 | tags=56%, list=59%, signal=137% | |
5085 | MORPHOGENESIS OF A BRANCHING EPITHELIUM | 102 | -0.15 | -0.61 | 0.955 | 0.973 | 1.000 | 17992 | tags=28%, list=33%, signal=42% | |
5086 | NUCLEOSOME POSITIONING | 12 | -0.25 | -0.61 | 0.859 | 0.973 | 1.000 | 38028 | tags=83%, list=70%, signal=274% | |
5087 | PURINERGIC NUCLEOTIDE RECEPTOR SIGNALING PATHWAY | 8 | -0.26 | -0.61 | 0.922 | 0.973 | 1.000 | 24316 | tags=50%, list=44%, signal=90% | |
5088 | POSITIVE REGULATION OF AXONOGENESIS | 89 | -0.16 | -0.61 | 0.956 | 0.973 | 1.000 | 38576 | tags=70%, list=71%, signal=236% | |
5089 | MUSCLE CONTRACTION | 401 | -0.13 | -0.61 | 0.974 | 0.973 | 1.000 | 24682 | tags=37%, list=45%, signal=67% | |
5090 | REGULATION OF PLATELET-DERIVED GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 27 | -0.19 | -0.61 | 0.937 | 0.973 | 1.000 | 29650 | tags=52%, list=54%, signal=113% | |
5091 | METANEPHRIC NEPHRON MORPHOGENESIS | 26 | -0.19 | -0.61 | 0.909 | 0.974 | 1.000 | 32287 | tags=58%, list=59%, signal=141% | |
5092 | LIPID HOMEOSTASIS | 169 | -0.15 | -0.61 | 0.975 | 0.974 | 1.000 | 26332 | tags=40%, list=48%, signal=77% | |
5093 | REGULATION OF EMBRYONIC DEVELOPMENT | 174 | -0.14 | -0.61 | 0.986 | 0.974 | 1.000 | 35345 | tags=59%, list=65%, signal=167% | |
5094 | RETINAL METABOLIC PROCESS | 23 | -0.22 | -0.61 | 0.868 | 0.974 | 1.000 | 41125 | tags=96%, list=75%, signal=386% | |
5095 | COGNITION | 250 | -0.14 | -0.61 | 0.992 | 0.974 | 1.000 | 28908 | tags=46%, list=53%, signal=97% | |
5096 | CENTRAL NERVOUS SYSTEM NEURON DIFFERENTIATION | 156 | -0.15 | -0.61 | 0.975 | 0.974 | 1.000 | 36829 | tags=65%, list=67%, signal=200% | |
5097 | REGULATION OF T-HELPER 17 TYPE IMMUNE RESPONSE | 13 | -0.25 | -0.61 | 0.885 | 0.974 | 1.000 | 27378 | tags=54%, list=50%, signal=108% | |
5098 | ZINC II ION TRANSPORT | 39 | -0.17 | -0.61 | 0.913 | 0.974 | 1.000 | 32908 | tags=64%, list=60%, signal=161% | |
5099 | NEGATIVE REGULATION OF LYASE ACTIVITY | 43 | -0.18 | -0.61 | 0.943 | 0.974 | 1.000 | 20474 | tags=33%, list=37%, signal=52% | |
5100 | RESPONSE TO FATTY ACID | 66 | -0.17 | -0.60 | 0.955 | 0.974 | 1.000 | 28908 | tags=48%, list=53%, signal=103% | |
5101 | EPITHELIAL STRUCTURE MAINTENANCE | 26 | -0.21 | -0.60 | 0.917 | 0.974 | 1.000 | 16158 | tags=35%, list=30%, signal=49% | |
5102 | REGULATION OF CYTOKINE BIOSYNTHETIC PROCESS | 113 | -0.18 | -0.60 | 0.884 | 0.974 | 1.000 | 21147 | tags=35%, list=39%, signal=58% | |
5103 | POSITIVE REGULATION OF T CELL DIFFERENTIATION IN THYMUS | 13 | -0.25 | -0.60 | 0.913 | 0.975 | 1.000 | 35416 | tags=77%, list=65%, signal=218% | |
5104 | POSITIVE REGULATION OF THYMOCYTE AGGREGATION | 13 | -0.25 | -0.60 | 0.913 | 0.975 | 1.000 | 35416 | tags=77%, list=65%, signal=218% | |
5105 | CELLULAR RESPONSE TO FLUID SHEAR STRESS | 31 | -0.20 | -0.60 | 0.909 | 0.975 | 1.000 | 23066 | tags=42%, list=42%, signal=72% | |
5106 | NEGATIVE REGULATION OF STRIATED MUSCLE CONTRACTION | 14 | -0.24 | -0.60 | 0.914 | 0.975 | 1.000 | 12625 | tags=29%, list=23%, signal=37% | |
5107 | REGULATION OF JAK-STAT CASCADE | 146 | -0.15 | -0.60 | 0.965 | 0.975 | 1.000 | 28934 | tags=47%, list=53%, signal=99% | |
5108 | REGULATION OF STAT CASCADE | 146 | -0.15 | -0.60 | 0.965 | 0.975 | 1.000 | 28934 | tags=47%, list=53%, signal=99% | |
5109 | SPERMATID NUCLEUS DIFFERENTIATION | 17 | -0.21 | -0.60 | 0.944 | 0.975 | 1.000 | 12044 | tags=24%, list=22%, signal=30% | |
5110 | POSITIVE REGULATION OF CYCLIC NUCLEOTIDE METABOLIC PROCESS | 164 | -0.15 | -0.60 | 0.964 | 0.975 | 1.000 | 30167 | tags=46%, list=55%, signal=102% | |
5111 | PITUITARY GLAND DEVELOPMENT | 21 | -0.20 | -0.60 | 0.916 | 0.974 | 1.000 | 41695 | tags=86%, list=76%, signal=361% | |
5112 | NEGATIVE REGULATION OF PROTEIN POLYMERIZATION | 65 | -0.16 | -0.60 | 0.979 | 0.974 | 1.000 | 19184 | tags=32%, list=35%, signal=50% | |
5113 | REGULATION OF PHOSPHOLIPASE A2 ACTIVITY | 25 | -0.19 | -0.60 | 0.918 | 0.975 | 1.000 | 33046 | tags=56%, list=60%, signal=141% | |
5114 | REGULATION OF VITAMIN D BIOSYNTHETIC PROCESS | 13 | -0.27 | -0.60 | 0.909 | 0.975 | 1.000 | 14790 | tags=31%, list=27%, signal=42% | |
5115 | NEURON RECOGNITION | 45 | -0.18 | -0.60 | 0.945 | 0.975 | 1.000 | 29044 | tags=47%, list=53%, signal=99% | |
5116 | NEGATIVE REGULATION OF G-PROTEIN COUPLED RECEPTOR PROTEIN SIGNALING PATHWAY | 60 | -0.16 | -0.60 | 0.955 | 0.975 | 1.000 | 15146 | tags=27%, list=28%, signal=37% | |
5117 | POSITIVE REGULATION OF POTASSIUM ION TRANSPORT | 57 | -0.15 | -0.60 | 0.986 | 0.975 | 1.000 | 32056 | tags=53%, list=59%, signal=127% | |
5118 | POSITIVE REGULATION OF T-HELPER 1 TYPE IMMUNE RESPONSE | 25 | -0.20 | -0.60 | 0.889 | 0.976 | 1.000 | 27378 | tags=52%, list=50%, signal=104% | |
5119 | CELLULAR ZINC ION HOMEOSTASIS | 25 | -0.20 | -0.60 | 0.945 | 0.976 | 1.000 | 40141 | tags=84%, list=73%, signal=316% | |
5120 | POSITIVE REGULATION OF ION TRANSPORT | 325 | -0.14 | -0.60 | 0.994 | 0.976 | 1.000 | 20983 | tags=34%, list=38%, signal=55% | |
5121 | NEGATIVE REGULATION OF PROTEIN ACTIVATION CASCADE | 25 | -0.22 | -0.60 | 0.900 | 0.976 | 1.000 | 23098 | tags=44%, list=42%, signal=76% | |
5122 | POSITIVE REGULATION OF INTERFERON-GAMMA PRODUCTION | 80 | -0.19 | -0.60 | 0.906 | 0.976 | 1.000 | 32149 | tags=60%, list=59%, signal=145% | |
5123 | POSITIVE REGULATION OF BONE MINERALIZATION | 70 | -0.16 | -0.60 | 0.977 | 0.976 | 1.000 | 30361 | tags=49%, list=56%, signal=109% | |
5124 | BLASTOCYST DEVELOPMENT | 13 | -0.20 | -0.60 | 0.959 | 0.976 | 1.000 | 37884 | tags=77%, list=69%, signal=250% | |
5125 | MIDBRAIN DOPAMINERGIC NEURON DIFFERENTIATION | 13 | -0.25 | -0.60 | 0.881 | 0.976 | 1.000 | 36829 | tags=77%, list=67%, signal=236% | |
5126 | NEUROLOGICAL SYSTEM PROCESS | 709 | -0.13 | -0.60 | 0.998 | 0.976 | 1.000 | 28719 | tags=44%, list=53%, signal=91% | |
5127 | CELL ADHESION MEDIATED BY INTEGRIN | 25 | -0.18 | -0.60 | 0.962 | 0.976 | 1.000 | 25181 | tags=40%, list=46%, signal=74% | |
5128 | REGULATION OF MUSCLE ORGAN DEVELOPMENT | 136 | -0.14 | -0.60 | 0.977 | 0.976 | 1.000 | 28184 | tags=43%, list=52%, signal=89% | |
5129 | REGULATION OF CALCIUM ION TRANSPORT | 312 | -0.14 | -0.60 | 0.988 | 0.976 | 1.000 | 23288 | tags=37%, list=43%, signal=63% | |
5130 | POSITIVE REGULATION OF ENDOTHELIAL CELL APOPTOTIC PROCESS | 28 | -0.20 | -0.60 | 0.905 | 0.976 | 1.000 | 42299 | tags=96%, list=77%, signal=426% | |
5131 | ADENYLATE CYCLASE-INHIBITING G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 80 | -0.16 | -0.60 | 0.942 | 0.976 | 1.000 | 30065 | tags=50%, list=55%, signal=111% | |
5132 | LEUKOCYTE MEDIATED IMMUNITY | 219 | -0.16 | -0.60 | 0.942 | 0.976 | 1.000 | 23476 | tags=37%, list=43%, signal=65% | |
5133 | POSITIVE REGULATION OF CALCIUM ION TRANSMEMBRANE TRANSPORT | 92 | -0.15 | -0.60 | 0.986 | 0.977 | 1.000 | 20627 | tags=34%, list=38%, signal=54% | |
5134 | HINDBRAIN DEVELOPMENT | 79 | -0.16 | -0.60 | 0.981 | 0.978 | 1.000 | 34829 | tags=58%, list=64%, signal=160% | |
5135 | BEHAVIOR | 337 | -0.13 | -0.60 | 0.984 | 0.978 | 1.000 | 21892 | tags=33%, list=40%, signal=54% | |
5136 | NEGATIVE REGULATION OF PROTEIN PROCESSING | 49 | -0.19 | -0.59 | 0.908 | 0.979 | 1.000 | 19340 | tags=37%, list=35%, signal=57% | |
5137 | NEGATIVE REGULATION OF PROTEIN MATURATION | 49 | -0.19 | -0.59 | 0.908 | 0.979 | 1.000 | 19340 | tags=37%, list=35%, signal=57% | |
5138 | PRONEPHROS DEVELOPMENT | 21 | -0.19 | -0.59 | 0.931 | 0.980 | 1.000 | 17093 | tags=29%, list=31%, signal=42% | |
5139 | NEURON CELLULAR HOMEOSTASIS | 14 | -0.21 | -0.59 | 0.947 | 0.980 | 1.000 | 37679 | tags=79%, list=69%, signal=253% | |
5140 | PHAGOCYTOSIS, RECOGNITION | 17 | -0.25 | -0.59 | 0.908 | 0.979 | 1.000 | 953 | tags=12%, list=2%, signal=12% | |
5141 | RESPONSE TO ZINC ION | 23 | -0.21 | -0.59 | 0.876 | 0.979 | 1.000 | 35163 | tags=70%, list=64%, signal=195% | |
5142 | CATECHOLAMINE METABOLIC PROCESS | 39 | -0.17 | -0.59 | 0.960 | 0.979 | 1.000 | 36946 | tags=64%, list=68%, signal=198% | |
5143 | CATECHOL-CONTAINING COMPOUND METABOLIC PROCESS | 39 | -0.17 | -0.59 | 0.960 | 0.979 | 1.000 | 36946 | tags=64%, list=68%, signal=198% | |
5144 | REGULATION OF SODIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 71 | -0.15 | -0.59 | 0.970 | 0.979 | 1.000 | 26088 | tags=45%, list=48%, signal=86% | |
5145 | DIVALENT INORGANIC CATION TRANSPORT | 423 | -0.13 | -0.59 | 0.978 | 0.980 | 1.000 | 33054 | tags=51%, list=60%, signal=129% | |
5146 | HORMONE SECRETION | 83 | -0.16 | -0.59 | 0.960 | 0.980 | 1.000 | 23143 | tags=36%, list=42%, signal=63% | |
5147 | REGULATION OF SODIUM ION TRANSPORT | 119 | -0.14 | -0.59 | 0.975 | 0.979 | 1.000 | 26088 | tags=43%, list=48%, signal=82% | |
5148 | NEGATIVE REGULATION OF CELLULAR SENESCENCE | 26 | -0.20 | -0.59 | 0.927 | 0.980 | 1.000 | 34776 | tags=69%, list=64%, signal=190% | |
5149 | POSITIVE REGULATION OF NUCLEAR DIVISION | 98 | -0.16 | -0.59 | 0.965 | 0.980 | 1.000 | 30219 | tags=53%, list=55%, signal=118% | |
5150 | NEGATIVE REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 30 | -0.18 | -0.59 | 0.978 | 0.980 | 1.000 | 37114 | tags=67%, list=68%, signal=207% | |
5151 | VASOCONSTRICTION | 32 | -0.19 | -0.59 | 0.910 | 0.980 | 1.000 | 28296 | tags=44%, list=52%, signal=91% | |
5152 | LIPOPROTEIN TRANSPORT | 17 | -0.21 | -0.59 | 0.914 | 0.980 | 1.000 | 41889 | tags=94%, list=77%, signal=402% | |
5153 | LIPOPROTEIN LOCALIZATION | 17 | -0.21 | -0.59 | 0.914 | 0.980 | 1.000 | 41889 | tags=94%, list=77%, signal=402% | |
5154 | POSITIVE REGULATION OF CYTOSOLIC CALCIUM ION CONCENTRATION | 251 | -0.14 | -0.59 | 0.960 | 0.980 | 1.000 | 32656 | tags=53%, list=60%, signal=130% | |
5155 | CARDIAC MUSCLE TISSUE MORPHOGENESIS | 74 | -0.15 | -0.59 | 0.951 | 0.980 | 1.000 | 32496 | tags=53%, list=59%, signal=130% | |
5156 | REGULATION OF STRIATED MUSCLE CELL APOPTOTIC PROCESS | 24 | -0.18 | -0.59 | 0.931 | 0.981 | 1.000 | 22078 | tags=38%, list=40%, signal=63% | |
5157 | REGULATION OF CARDIAC MUSCLE HYPERTROPHY | 56 | -0.17 | -0.59 | 0.973 | 0.981 | 1.000 | 26088 | tags=43%, list=48%, signal=82% | |
5158 | REGULATION OF MUSCLE HYPERTROPHY | 56 | -0.17 | -0.59 | 0.973 | 0.980 | 1.000 | 26088 | tags=43%, list=48%, signal=82% | |
5159 | PRESYNAPTIC MEMBRANE ORGANIZATION | 33 | -0.18 | -0.59 | 0.941 | 0.981 | 1.000 | 18558 | tags=33%, list=34%, signal=50% | |
5160 | DRUG TRANSPORT | 30 | -0.18 | -0.59 | 0.956 | 0.981 | 1.000 | 31236 | tags=60%, list=57%, signal=140% | |
5161 | POSITIVE REGULATION OF PROTEIN EXIT FROM ENDOPLASMIC RETICULUM | 17 | -0.21 | -0.59 | 0.922 | 0.981 | 1.000 | 34366 | tags=76%, list=63%, signal=206% | |
5162 | DIVALENT METAL ION TRANSPORT | 418 | -0.13 | -0.59 | 0.972 | 0.981 | 1.000 | 33054 | tags=51%, list=60%, signal=128% | |
5163 | NEURON CELL-CELL ADHESION | 33 | -0.19 | -0.59 | 0.931 | 0.981 | 1.000 | 7877 | tags=15%, list=14%, signal=18% | |
5164 | NEURAL CREST CELL DIFFERENTIATION | 54 | -0.15 | -0.59 | 0.960 | 0.982 | 1.000 | 36790 | tags=61%, list=67%, signal=187% | |
5165 | POSITIVE REGULATION OF BLOOD PRESSURE | 16 | -0.21 | -0.59 | 0.934 | 0.982 | 1.000 | 24337 | tags=44%, list=45%, signal=79% | |
5166 | NEGATIVE REGULATION OF VITAMIN METABOLIC PROCESS | 6 | -0.27 | -0.59 | 0.948 | 0.982 | 1.000 | 4070 | tags=17%, list=7%, signal=18% | |
5167 | REGULATION OF CALCIUM ION TRANSMEMBRANE TRANSPORT | 193 | -0.14 | -0.59 | 0.998 | 0.982 | 1.000 | 20691 | tags=33%, list=38%, signal=52% | |
5168 | CELLULAR RESPONSE TO LIPOPOLYSACCHARIDE | 140 | -0.19 | -0.59 | 0.925 | 0.982 | 1.000 | 7557 | tags=16%, list=14%, signal=19% | |
5169 | REGULATION OF NEUROBLAST PROLIFERATION | 38 | -0.18 | -0.59 | 0.928 | 0.983 | 1.000 | 39506 | tags=79%, list=72%, signal=284% | |
5170 | PURINERGIC RECEPTOR SIGNALING PATHWAY | 10 | -0.23 | -0.59 | 0.954 | 0.983 | 1.000 | 24316 | tags=50%, list=44%, signal=90% | |
5171 | LATERAL MESODERM DEVELOPMENT | 11 | -0.21 | -0.59 | 0.944 | 0.983 | 1.000 | 34701 | tags=73%, list=63%, signal=199% | |
5172 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT3 PROTEIN | 73 | -0.15 | -0.58 | 0.966 | 0.984 | 1.000 | 36468 | tags=60%, list=67%, signal=181% | |
5173 | INTERLEUKIN-1 PRODUCTION | 25 | -0.21 | -0.58 | 0.899 | 0.983 | 1.000 | 41418 | tags=92%, list=76%, signal=379% | |
5174 | ACIDIC AMINO ACID TRANSPORT | 28 | -0.18 | -0.58 | 0.962 | 0.983 | 1.000 | 32527 | tags=64%, list=59%, signal=159% | |
5175 | L-GLUTAMATE TRANSPORT | 28 | -0.18 | -0.58 | 0.962 | 0.983 | 1.000 | 32527 | tags=64%, list=59%, signal=159% | |
5176 | POSITIVE REGULATION OF NUCLEOTIDE BIOSYNTHETIC PROCESS | 149 | -0.15 | -0.58 | 0.973 | 0.983 | 1.000 | 30167 | tags=44%, list=55%, signal=99% | |
5177 | POSITIVE REGULATION OF PURINE NUCLEOTIDE BIOSYNTHETIC PROCESS | 149 | -0.15 | -0.58 | 0.973 | 0.983 | 1.000 | 30167 | tags=44%, list=55%, signal=99% | |
5178 | POSITIVE REGULATION OF AXON EXTENSION | 53 | -0.16 | -0.58 | 0.929 | 0.983 | 1.000 | 28038 | tags=47%, list=51%, signal=97% | |
5179 | MODULATION OF EXCITATORY POSTSYNAPTIC POTENTIAL | 53 | -0.16 | -0.58 | 0.941 | 0.982 | 1.000 | 18246 | tags=28%, list=33%, signal=42% | |
5180 | LYMPHANGIOGENESIS | 30 | -0.18 | -0.58 | 0.946 | 0.983 | 1.000 | 36113 | tags=67%, list=66%, signal=196% | |
5181 | REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 43 | -0.16 | -0.58 | 0.952 | 0.983 | 1.000 | 31828 | tags=56%, list=58%, signal=133% | |
5182 | NEGATIVE REGULATION OF MAST CELL ACTIVATION | 16 | -0.21 | -0.58 | 0.932 | 0.983 | 1.000 | 4520 | tags=13%, list=8%, signal=14% | |
5183 | POSITIVE REGULATION OF PHOSPHATIDYLINOSITOL 3-KINASE SIGNALING | 122 | -0.15 | -0.58 | 0.940 | 0.983 | 1.000 | 26432 | tags=40%, list=48%, signal=78% | |
5184 | ESTROGEN METABOLIC PROCESS | 30 | -0.18 | -0.58 | 0.924 | 0.983 | 1.000 | 41759 | tags=87%, list=76%, signal=367% | |
5185 | REGULATION OF CYTOSOLIC CALCIUM ION CONCENTRATION | 270 | -0.14 | -0.58 | 0.971 | 0.983 | 1.000 | 32656 | tags=52%, list=60%, signal=129% | |
5186 | PEPTIDE HORMONE PROCESSING | 51 | -0.17 | -0.58 | 0.930 | 0.983 | 1.000 | 23989 | tags=35%, list=44%, signal=63% | |
5187 | MESODERM FORMATION | 68 | -0.16 | -0.58 | 0.985 | 0.984 | 1.000 | 35838 | tags=66%, list=66%, signal=192% | |
5188 | REGULATION OF RESPONSE TO WOUNDING | 531 | -0.15 | -0.58 | 0.977 | 0.984 | 1.000 | 33180 | tags=56%, list=61%, signal=140% | |
5189 | INNERVATION | 16 | -0.21 | -0.58 | 0.945 | 0.985 | 1.000 | 36858 | tags=69%, list=67%, signal=211% | |
5190 | GLUTAMATE RECEPTOR SIGNALING PATHWAY | 87 | -0.15 | -0.58 | 0.947 | 0.985 | 1.000 | 9679 | tags=15%, list=18%, signal=18% | |
5191 | NEUROTRANSMITTER TRANSPORT | 185 | -0.14 | -0.58 | 0.994 | 0.985 | 1.000 | 37177 | tags=63%, list=68%, signal=197% | |
5192 | GLYCEROL TRANSPORT | 10 | -0.22 | -0.58 | 0.942 | 0.985 | 1.000 | 9973 | tags=20%, list=18%, signal=24% | |
5193 | REGULATION OF CARDIAC MUSCLE TISSUE GROWTH | 51 | -0.16 | -0.58 | 0.944 | 0.985 | 1.000 | 28154 | tags=43%, list=51%, signal=89% | |
5194 | C-TERMINAL PROTEIN DEGLUTAMYLATION | 10 | -0.24 | -0.58 | 0.927 | 0.985 | 1.000 | 41416 | tags=100%, list=76%, signal=412% | |
5195 | REGULATION OF REGULATORY T CELL DIFFERENTIATION | 22 | -0.20 | -0.58 | 0.900 | 0.985 | 1.000 | 16993 | tags=32%, list=31%, signal=46% | |
5196 | NEGATIVE REGULATION OF LAMELLIPODIUM ORGANIZATION | 9 | -0.25 | -0.58 | 0.928 | 0.986 | 1.000 | 1099 | tags=11%, list=2%, signal=11% | |
5197 | INDOLE-CONTAINING COMPOUND METABOLIC PROCESS | 31 | -0.18 | -0.58 | 0.942 | 0.986 | 1.000 | 23107 | tags=39%, list=42%, signal=67% | |
5198 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT PROTEIN | 108 | -0.15 | -0.58 | 0.966 | 0.985 | 1.000 | 28934 | tags=46%, list=53%, signal=98% | |
5199 | POSITIVE REGULATION OF GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR PRODUCTION | 12 | -0.24 | -0.58 | 0.960 | 0.985 | 1.000 | 32149 | tags=67%, list=59%, signal=162% | |
5200 | SEX DIFFERENTIATION | 169 | -0.14 | -0.58 | 0.981 | 0.986 | 1.000 | 31392 | tags=49%, list=57%, signal=114% | |
5201 | POSITIVE REGULATION OF INTERFERON-GAMMA SECRETION | 9 | -0.26 | -0.58 | 0.928 | 0.986 | 1.000 | 36178 | tags=78%, list=66%, signal=230% | |
5202 | NEGATIVE REGULATION OF METANEPHROS DEVELOPMENT | 16 | -0.21 | -0.58 | 0.939 | 0.985 | 1.000 | 19886 | tags=38%, list=36%, signal=59% | |
5203 | CEREBRAL CORTEX NEURON DIFFERENTIATION | 13 | -0.23 | -0.58 | 0.914 | 0.986 | 1.000 | 36712 | tags=77%, list=67%, signal=234% | |
5204 | REGULATION OF HAIR CYCLE | 30 | -0.18 | -0.58 | 0.954 | 0.986 | 1.000 | 28867 | tags=50%, list=53%, signal=106% | |
5205 | POSITIVE REGULATION OF SPINDLE CHECKPOINT | 15 | -0.23 | -0.58 | 0.892 | 0.986 | 1.000 | 31967 | tags=67%, list=58%, signal=160% | |
5206 | POSITIVE REGULATION OF CELL CYCLE CHECKPOINT | 15 | -0.23 | -0.58 | 0.892 | 0.986 | 1.000 | 31967 | tags=67%, list=58%, signal=160% | |
5207 | INTRA-S DNA DAMAGE CHECKPOINT | 10 | -0.24 | -0.58 | 0.922 | 0.986 | 1.000 | 26545 | tags=60%, list=49%, signal=117% | |
5208 | NEGATIVE REGULATION OF SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 51 | -0.18 | -0.58 | 0.940 | 0.986 | 1.000 | 9326 | tags=18%, list=17%, signal=21% | |
5209 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 51 | -0.18 | -0.58 | 0.940 | 0.986 | 1.000 | 9326 | tags=18%, list=17%, signal=21% | |
5210 | STRIATED MUSCLE CELL DEVELOPMENT | 141 | -0.14 | -0.58 | 0.991 | 0.986 | 1.000 | 32590 | tags=57%, list=60%, signal=140% | |
5211 | HEART FORMATION | 11 | -0.22 | -0.58 | 0.952 | 0.986 | 1.000 | 35345 | tags=73%, list=65%, signal=206% | |
5212 | POSITIVE REGULATION OF VASCULATURE DEVELOPMENT | 233 | -0.14 | -0.58 | 0.985 | 0.986 | 1.000 | 35476 | tags=58%, list=65%, signal=166% | |
5213 | SUBSTRATE-DEPENDENT CELL MIGRATION, CELL EXTENSION | 8 | -0.23 | -0.58 | 0.950 | 0.986 | 1.000 | 37553 | tags=75%, list=69%, signal=239% | |
5214 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL DIFFERENTIATION | 7 | -0.27 | -0.58 | 0.956 | 0.986 | 1.000 | 32921 | tags=71%, list=60%, signal=180% | |
5215 | N-GLYCAN PROCESSING | 27 | -0.18 | -0.57 | 0.921 | 0.986 | 1.000 | 33119 | tags=63%, list=61%, signal=160% | |
5216 | MORPHOGENESIS OF A BRANCHING STRUCTURE | 114 | -0.14 | -0.57 | 0.956 | 0.987 | 1.000 | 17992 | tags=28%, list=33%, signal=42% | |
5217 | MYOBLAST DIFFERENTIATION | 58 | -0.16 | -0.57 | 0.981 | 0.987 | 1.000 | 38427 | tags=71%, list=70%, signal=238% | |
5218 | REGULATION OF METANEPHRIC GLOMERULUS DEVELOPMENT | 11 | -0.25 | -0.57 | 0.917 | 0.987 | 1.000 | 40903 | tags=100%, list=75%, signal=397% | |
5219 | REGULATION OF SYNAPSE MATURATION | 21 | -0.20 | -0.57 | 0.925 | 0.987 | 1.000 | 1161 | tags=10%, list=2%, signal=10% | |
5220 | POSITIVE REGULATION OF POSITIVE CHEMOTAXIS | 25 | -0.17 | -0.57 | 0.957 | 0.988 | 1.000 | 1605 | tags=8%, list=3%, signal=8% | |
5221 | NEGATIVE REGULATION OF PHOSPHOLIPASE ACTIVITY | 17 | -0.21 | -0.57 | 0.943 | 0.987 | 1.000 | 33046 | tags=65%, list=60%, signal=164% | |
5222 | GAP JUNCTION ASSEMBLY | 13 | -0.21 | -0.57 | 0.942 | 0.987 | 1.000 | 22233 | tags=38%, list=41%, signal=65% | |
5223 | PYRIMIDINE NUCLEOSIDE CATABOLIC PROCESS | 38 | -0.17 | -0.57 | 0.972 | 0.987 | 1.000 | 35532 | tags=71%, list=65%, signal=203% | |
5224 | DRUG TRANSMEMBRANE TRANSPORT | 23 | -0.20 | -0.57 | 0.948 | 0.987 | 1.000 | 22797 | tags=43%, list=42%, signal=75% | |
5225 | REGULATION OF NF-KAPPAB IMPORT INTO NUCLEUS | 69 | -0.19 | -0.57 | 0.948 | 0.987 | 1.000 | 39400 | tags=78%, list=72%, signal=280% | |
5226 | POSTSYNAPTIC MEMBRANE ORGANIZATION | 29 | -0.18 | -0.57 | 0.939 | 0.987 | 1.000 | 8636 | tags=17%, list=16%, signal=20% | |
5227 | NEGATIVE REGULATION OF AMINE TRANSPORT | 11 | -0.23 | -0.57 | 0.933 | 0.987 | 1.000 | 36946 | tags=73%, list=68%, signal=224% | |
5228 | POSITIVE REGULATION OF CARDIAC MUSCLE CELL DIFFERENTIATION | 14 | -0.22 | -0.57 | 0.922 | 0.987 | 1.000 | 27588 | tags=50%, list=50%, signal=101% | |
5229 | NATURAL KILLER CELL MEDIATED IMMUNITY | 24 | -0.19 | -0.57 | 0.960 | 0.987 | 1.000 | 24591 | tags=46%, list=45%, signal=83% | |
5230 | ASPARTATE TRANSPORT | 16 | -0.19 | -0.57 | 0.943 | 0.987 | 1.000 | 6391 | tags=19%, list=12%, signal=21% | |
5231 | REGULATION OF VENTRICULAR CARDIAC MUSCLE CELL MEMBRANE REPOLARIZATION | 21 | -0.17 | -0.57 | 0.957 | 0.987 | 1.000 | 32056 | tags=52%, list=59%, signal=127% | |
5232 | NEGATIVE REGULATION OF LEUKOCYTE PROLIFERATION | 80 | -0.18 | -0.57 | 0.923 | 0.987 | 1.000 | 24197 | tags=40%, list=44%, signal=72% | |
5233 | REGULATION OF LIPOPROTEIN LIPASE ACTIVITY | 24 | -0.20 | -0.57 | 0.919 | 0.987 | 1.000 | 4646 | tags=13%, list=8%, signal=14% | |
5234 | ENTERIC NERVOUS SYSTEM DEVELOPMENT | 11 | -0.23 | -0.57 | 0.956 | 0.987 | 1.000 | 617 | tags=9%, list=1%, signal=9% | |
5235 | CELL DIFFERENTIATION IN HINDBRAIN | 20 | -0.19 | -0.57 | 0.932 | 0.988 | 1.000 | 33770 | tags=60%, list=62%, signal=157% | |
5236 | NEGATIVE REGULATION OF EXOCYTOSIS | 34 | -0.18 | -0.57 | 0.959 | 0.988 | 1.000 | 37114 | tags=68%, list=68%, signal=210% | |
5237 | TRANSMISSION OF NERVE IMPULSE | 36 | -0.17 | -0.57 | 0.947 | 0.988 | 1.000 | 38258 | tags=69%, list=70%, signal=231% | |
5238 | SIALYLATION | 48 | -0.16 | -0.57 | 0.958 | 0.989 | 1.000 | 18690 | tags=29%, list=34%, signal=44% | |
5239 | FEMALE SEX DIFFERENTIATION | 54 | -0.16 | -0.57 | 0.970 | 0.989 | 1.000 | 6539 | tags=13%, list=12%, signal=15% | |
5240 | MEMBRANE DEPOLARIZATION | 77 | -0.15 | -0.57 | 0.953 | 0.989 | 1.000 | 26612 | tags=42%, list=49%, signal=81% | |
5241 | REGULATION OF OSTEOBLAST PROLIFERATION | 40 | -0.17 | -0.57 | 0.938 | 0.989 | 1.000 | 37825 | tags=70%, list=69%, signal=227% | |
5242 | LOW-DENSITY LIPOPROTEIN PARTICLE REMODELING | 13 | -0.22 | -0.57 | 0.947 | 0.989 | 1.000 | 6711 | tags=15%, list=12%, signal=18% | |
5243 | REGULATION OF GLUTAMATE RECEPTOR SIGNALING PATHWAY | 54 | -0.17 | -0.57 | 0.932 | 0.989 | 1.000 | 972 | tags=7%, list=2%, signal=8% | |
5244 | REGULATION OF T-HELPER 1 TYPE IMMUNE RESPONSE | 31 | -0.19 | -0.57 | 0.890 | 0.988 | 1.000 | 27378 | tags=48%, list=50%, signal=97% | |
5245 | POSITIVE REGULATION OF SMOOTHENED SIGNALING PATHWAY | 19 | -0.20 | -0.57 | 0.935 | 0.989 | 1.000 | 18961 | tags=37%, list=35%, signal=56% | |
5246 | MESENCHYMAL TO EPITHELIAL TRANSITION | 26 | -0.19 | -0.57 | 0.934 | 0.989 | 1.000 | 32287 | tags=58%, list=59%, signal=141% | |
5247 | REGULATION OF HEART CONTRACTION | 413 | -0.13 | -0.57 | 0.981 | 0.989 | 1.000 | 24523 | tags=35%, list=45%, signal=64% | |
5248 | CHONDROITIN SULFATE CATABOLIC PROCESS | 46 | -0.18 | -0.57 | 0.927 | 0.989 | 1.000 | 38582 | tags=74%, list=71%, signal=251% | |
5249 | POSITIVE REGULATION OF CALCIUM ION TRANSPORT | 149 | -0.14 | -0.56 | 0.992 | 0.990 | 1.000 | 23288 | tags=38%, list=43%, signal=65% | |
5250 | POSITIVE REGULATION OF G-PROTEIN COUPLED RECEPTOR PROTEIN SIGNALING PATHWAY | 20 | -0.18 | -0.56 | 0.970 | 0.990 | 1.000 | 32307 | tags=55%, list=59%, signal=134% | |
5251 | MULTI-ORGANISM BEHAVIOR | 85 | -0.14 | -0.56 | 0.972 | 0.989 | 1.000 | 33239 | tags=58%, list=61%, signal=147% | |
5252 | T CELL CHEMOTAXIS | 10 | -0.28 | -0.56 | 0.934 | 0.989 | 1.000 | 13668 | tags=30%, list=25%, signal=40% | |
5253 | REGULATION OF CELL ADHESION MEDIATED BY INTEGRIN | 75 | -0.16 | -0.56 | 0.981 | 0.989 | 1.000 | 30152 | tags=51%, list=55%, signal=113% | |
5254 | PLASMA LIPOPROTEIN PARTICLE CLEARANCE | 49 | -0.18 | -0.56 | 0.919 | 0.989 | 1.000 | 21720 | tags=37%, list=40%, signal=61% | |
5255 | NEGATIVE REGULATION OF B CELL MEDIATED IMMUNITY | 13 | -0.23 | -0.56 | 0.956 | 0.989 | 1.000 | 9310 | tags=23%, list=17%, signal=28% | |
5256 | NEGATIVE REGULATION OF IMMUNOGLOBULIN MEDIATED IMMUNE RESPONSE | 13 | -0.23 | -0.56 | 0.956 | 0.989 | 1.000 | 9310 | tags=23%, list=17%, signal=28% | |
5257 | INTERLEUKIN-1 BETA SECRETION | 22 | -0.23 | -0.56 | 0.916 | 0.989 | 1.000 | 41418 | tags=95%, list=76%, signal=394% | |
5258 | PROTEIN SIDE CHAIN DEGLUTAMYLATION | 9 | -0.26 | -0.56 | 0.928 | 0.989 | 1.000 | 40704 | tags=100%, list=74%, signal=391% | |
5259 | ADRENAL GLAND DEVELOPMENT | 30 | -0.17 | -0.56 | 0.959 | 0.989 | 1.000 | 41491 | tags=80%, list=76%, signal=332% | |
5260 | RETROGRADE AXONAL TRANSPORT | 12 | -0.21 | -0.56 | 0.945 | 0.989 | 1.000 | 6984 | tags=17%, list=13%, signal=19% | |
5261 | PATTERN SPECIFICATION INVOLVED IN KIDNEY DEVELOPMENT | 13 | -0.21 | -0.56 | 0.952 | 0.989 | 1.000 | 17093 | tags=31%, list=31%, signal=45% | |
5262 | RENAL SYSTEM PATTERN SPECIFICATION | 13 | -0.21 | -0.56 | 0.952 | 0.989 | 1.000 | 17093 | tags=31%, list=31%, signal=45% | |
5263 | ANION HOMEOSTASIS | 78 | -0.16 | -0.56 | 0.956 | 0.989 | 1.000 | 24557 | tags=41%, list=45%, signal=74% | |
5264 | CELLULAR DEFENSE RESPONSE | 103 | -0.15 | -0.56 | 0.962 | 0.989 | 1.000 | 36677 | tags=64%, list=67%, signal=194% | |
5265 | CELL FATE DETERMINATION | 38 | -0.16 | -0.56 | 0.960 | 0.989 | 1.000 | 17346 | tags=29%, list=32%, signal=42% | |
5266 | NEGATIVE REGULATION OF CELL ADHESION MEDIATED BY INTEGRIN | 12 | -0.23 | -0.56 | 0.924 | 0.989 | 1.000 | 36972 | tags=83%, list=68%, signal=257% | |
5267 | REGULATION OF OOCYTE DEVELOPMENT | 8 | -0.24 | -0.56 | 0.949 | 0.989 | 1.000 | 18711 | tags=38%, list=34%, signal=57% | |
5268 | NEGATIVE REGULATION OF CELL PROLIFERATION INVOLVED IN KIDNEY DEVELOPMENT | 14 | -0.22 | -0.56 | 0.921 | 0.989 | 1.000 | 19751 | tags=36%, list=36%, signal=56% | |
5269 | POSITIVE REGULATION OF PROTEIN MATURATION | 30 | -0.17 | -0.56 | 0.967 | 0.989 | 1.000 | 20886 | tags=37%, list=38%, signal=59% | |
5270 | REGULATION OF INTERLEUKIN-2 PRODUCTION | 95 | -0.16 | -0.56 | 0.981 | 0.989 | 1.000 | 29516 | tags=45%, list=54%, signal=98% | |
5271 | DERMATAN SULFATE METABOLIC PROCESS | 37 | -0.18 | -0.56 | 0.942 | 0.989 | 1.000 | 37972 | tags=68%, list=69%, signal=221% | |
5272 | POSITIVE REGULATION OF CAMP METABOLIC PROCESS | 135 | -0.14 | -0.56 | 0.970 | 0.989 | 1.000 | 30167 | tags=44%, list=55%, signal=99% | |
5273 | MESONEPHRIC EPITHELIUM DEVELOPMENT | 75 | -0.15 | -0.56 | 0.965 | 0.989 | 1.000 | 17093 | tags=25%, list=31%, signal=37% | |
5274 | MESONEPHRIC TUBULE DEVELOPMENT | 75 | -0.15 | -0.56 | 0.965 | 0.989 | 1.000 | 17093 | tags=25%, list=31%, signal=37% | |
5275 | REGULATION OF CIRCADIAN SLEEP/WAKE CYCLE | 13 | -0.21 | -0.56 | 0.947 | 0.989 | 1.000 | 15325 | tags=31%, list=28%, signal=43% | |
5276 | REGULATION OF CAMP BIOSYNTHETIC PROCESS | 166 | -0.14 | -0.56 | 0.958 | 0.989 | 1.000 | 30167 | tags=44%, list=55%, signal=98% | |
5277 | REGULATION OF STRIATED MUSCLE TISSUE DEVELOPMENT | 132 | -0.13 | -0.56 | 0.979 | 0.989 | 1.000 | 28184 | tags=42%, list=52%, signal=87% | |
5278 | NEGATIVE REGULATION OF RESPONSE TO REACTIVE OXYGEN SPECIES | 32 | -0.17 | -0.56 | 0.992 | 0.988 | 1.000 | 9001 | tags=19%, list=16%, signal=22% | |
5279 | DIGESTION | 135 | -0.14 | -0.56 | 0.985 | 0.989 | 1.000 | 21434 | tags=34%, list=39%, signal=56% | |
5280 | EYE PIGMENTATION | 11 | -0.21 | -0.56 | 0.980 | 0.988 | 1.000 | 8136 | tags=18%, list=15%, signal=21% | |
5281 | UREA CYCLE | 15 | -0.21 | -0.56 | 0.935 | 0.989 | 1.000 | 23078 | tags=40%, list=42%, signal=69% | |
5282 | POSITIVE REGULATION OF MACROPHAGE DERIVED FOAM CELL DIFFERENTIATION | 27 | -0.17 | -0.56 | 0.932 | 0.988 | 1.000 | 31725 | tags=59%, list=58%, signal=141% | |
5283 | REGULATION OF ENDOTHELIAL CELL APOPTOTIC PROCESS | 75 | -0.16 | -0.56 | 0.978 | 0.989 | 1.000 | 43016 | tags=85%, list=79%, signal=400% | |
5284 | HORMONE TRANSPORT | 87 | -0.15 | -0.56 | 0.979 | 0.989 | 1.000 | 39624 | tags=69%, list=72%, signal=250% | |
5285 | SPINAL CORD PATTERNING | 14 | -0.21 | -0.56 | 0.942 | 0.989 | 1.000 | 35657 | tags=79%, list=65%, signal=226% | |
5286 | NEURAL CREST CELL DEVELOPMENT | 46 | -0.15 | -0.56 | 0.959 | 0.989 | 1.000 | 36790 | tags=59%, list=67%, signal=179% | |
5287 | REGULATION OF MUSCLE TISSUE DEVELOPMENT | 134 | -0.13 | -0.56 | 0.979 | 0.989 | 1.000 | 28184 | tags=43%, list=52%, signal=88% | |
5288 | NEGATIVE REGULATION OF COMPLEMENT ACTIVATION | 22 | -0.21 | -0.56 | 0.913 | 0.989 | 1.000 | 23098 | tags=45%, list=42%, signal=79% | |
5289 | REGULATION OF CELLULAR EXTRAVASATION | 22 | -0.20 | -0.56 | 0.950 | 0.989 | 1.000 | 41664 | tags=82%, list=76%, signal=344% | |
5290 | REGULATION OF CELL MATURATION | 9 | -0.25 | -0.56 | 0.940 | 0.989 | 1.000 | 29852 | tags=56%, list=55%, signal=122% | |
5291 | REGULATION OF STEROID BIOSYNTHETIC PROCESS | 63 | -0.16 | -0.56 | 0.968 | 0.989 | 1.000 | 21017 | tags=33%, list=38%, signal=54% | |
5292 | MUSCLE STRUCTURE DEVELOPMENT | 537 | -0.12 | -0.56 | 0.998 | 0.989 | 1.000 | 32862 | tags=52%, list=60%, signal=130% | |
5293 | SENSORY PERCEPTION OF TASTE | 46 | -0.17 | -0.56 | 0.958 | 0.989 | 1.000 | 37888 | tags=67%, list=69%, signal=219% | |
5294 | REGULATION OF BONE REMODELING | 58 | -0.16 | -0.56 | 0.988 | 0.989 | 1.000 | 39506 | tags=72%, list=72%, signal=261% | |
5295 | LEUKOCYTE PROLIFERATION | 61 | -0.17 | -0.55 | 0.940 | 0.990 | 1.000 | 30091 | tags=54%, list=55%, signal=120% | |
5296 | CELL MIGRATION INVOLVED IN SPROUTING ANGIOGENESIS | 34 | -0.17 | -0.55 | 0.962 | 0.991 | 1.000 | 29286 | tags=50%, list=54%, signal=108% | |
5297 | REGULATION OF AMINE TRANSPORT | 58 | -0.14 | -0.55 | 0.982 | 0.991 | 1.000 | 14129 | tags=24%, list=26%, signal=33% | |
5298 | REGULATION OF MEMORY T CELL DIFFERENTIATION | 12 | -0.22 | -0.55 | 0.963 | 0.991 | 1.000 | 30991 | tags=58%, list=57%, signal=135% | |
5299 | MYELOID LEUKOCYTE MIGRATION | 96 | -0.17 | -0.55 | 0.932 | 0.991 | 1.000 | 22408 | tags=33%, list=41%, signal=56% | |
5300 | REGULATION OF ALPHA-AMINO-3-HYDROXY-5-METHYL-4-ISOXAZOLE PROPIONATE SELECTIVE GLUTAMATE RECEPTOR ACTIVITY | 42 | -0.17 | -0.55 | 0.944 | 0.991 | 1.000 | 517 | tags=7%, list=1%, signal=7% | |
5301 | REGULATION OF PODOSOME ASSEMBLY | 18 | -0.20 | -0.55 | 0.953 | 0.991 | 1.000 | 11352 | tags=22%, list=21%, signal=28% | |
5302 | NEGATIVE REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS | 12 | -0.23 | -0.55 | 0.939 | 0.991 | 1.000 | 5907 | tags=17%, list=11%, signal=19% | |
5303 | DEFENSE RESPONSE TO BACTERIUM | 227 | -0.15 | -0.55 | 0.964 | 0.992 | 1.000 | 25181 | tags=39%, list=46%, signal=72% | |
5304 | PROSTAGLANDIN BIOSYNTHETIC PROCESS | 39 | -0.17 | -0.55 | 0.946 | 0.992 | 1.000 | 39148 | tags=74%, list=72%, signal=262% | |
5305 | PROSTANOID BIOSYNTHETIC PROCESS | 39 | -0.17 | -0.55 | 0.946 | 0.992 | 1.000 | 39148 | tags=74%, list=72%, signal=262% | |
5306 | CHLORIDE TRANSMEMBRANE TRANSPORT | 117 | -0.14 | -0.55 | 0.983 | 0.992 | 1.000 | 21324 | tags=32%, list=39%, signal=53% | |
5307 | REGULATION OF SEQUESTERING OF CALCIUM ION | 202 | -0.13 | -0.55 | 0.996 | 0.992 | 1.000 | 33666 | tags=55%, list=62%, signal=144% | |
5308 | NEGATIVE REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 27 | -0.17 | -0.55 | 0.949 | 0.992 | 1.000 | 19469 | tags=33%, list=36%, signal=52% | |
5309 | HAIR FOLLICLE MORPHOGENESIS | 26 | -0.19 | -0.55 | 0.920 | 0.992 | 1.000 | 15881 | tags=31%, list=29%, signal=43% | |
5310 | MEIOTIC CHROMOSOME SEPARATION | 11 | -0.20 | -0.55 | 0.971 | 0.993 | 1.000 | 2271 | tags=9%, list=4%, signal=9% | |
5311 | BICARBONATE TRANSPORT | 75 | -0.16 | -0.55 | 0.964 | 0.993 | 1.000 | 40120 | tags=75%, list=73%, signal=280% | |
5312 | PHAGOCYTOSIS, ENGULFMENT | 34 | -0.16 | -0.55 | 0.957 | 0.993 | 1.000 | 41845 | tags=85%, list=77%, signal=363% | |
5313 | REGULATION OF CHONDROCYTE DIFFERENTIATION | 56 | -0.14 | -0.55 | 0.994 | 0.993 | 1.000 | 33764 | tags=57%, list=62%, signal=149% | |
5314 | POSITIVE REGULATION OF JAK-STAT CASCADE | 100 | -0.14 | -0.55 | 0.962 | 0.993 | 1.000 | 28614 | tags=43%, list=52%, signal=90% | |
5315 | POSITIVE REGULATION OF STAT CASCADE | 100 | -0.14 | -0.55 | 0.962 | 0.993 | 1.000 | 28614 | tags=43%, list=52%, signal=90% | |
5316 | REGULATION OF AXON GUIDANCE | 25 | -0.18 | -0.55 | 0.968 | 0.993 | 1.000 | 38370 | tags=72%, list=70%, signal=241% | |
5317 | MYOFIBRIL ASSEMBLY | 82 | -0.14 | -0.55 | 0.977 | 0.994 | 1.000 | 33704 | tags=60%, list=62%, signal=156% | |
5318 | LENS FIBER CELL DEVELOPMENT | 10 | -0.23 | -0.55 | 0.952 | 0.994 | 1.000 | 33704 | tags=70%, list=62%, signal=182% | |
5319 | CARDIAC MUSCLE TISSUE DEVELOPMENT | 182 | -0.12 | -0.55 | 0.992 | 0.993 | 1.000 | 32149 | tags=52%, list=59%, signal=125% | |
5320 | POSITIVE REGULATION OF DEVELOPMENTAL GROWTH | 190 | -0.13 | -0.55 | 0.984 | 0.993 | 1.000 | 28294 | tags=42%, list=52%, signal=87% | |
5321 | CHRONIC INFLAMMATORY RESPONSE | 12 | -0.24 | -0.55 | 0.940 | 0.994 | 1.000 | 5047 | tags=17%, list=9%, signal=18% | |
5322 | MULTICELLULAR ORGANISMAL SIGNALING | 316 | -0.12 | -0.55 | 0.986 | 0.994 | 1.000 | 23366 | tags=33%, list=43%, signal=57% | |
5323 | REGULATION OF INOSITOL PHOSPHATE BIOSYNTHETIC PROCESS | 15 | -0.23 | -0.54 | 0.952 | 0.994 | 1.000 | 3751 | tags=13%, list=7%, signal=14% | |
5324 | NEGATIVE REGULATION OF LIPOPROTEIN METABOLIC PROCESS | 13 | -0.20 | -0.54 | 0.962 | 0.994 | 1.000 | 37449 | tags=77%, list=68%, signal=244% | |
5325 | REGULATION OF ACUTE INFLAMMATORY RESPONSE | 92 | -0.16 | -0.54 | 0.971 | 0.994 | 1.000 | 28382 | tags=49%, list=52%, signal=102% | |
5326 | VASCULAR SMOOTH MUSCLE CONTRACTION | 30 | -0.17 | -0.54 | 0.948 | 0.993 | 1.000 | 28296 | tags=43%, list=52%, signal=90% | |
5327 | INTERLEUKIN-1 BETA PRODUCTION | 23 | -0.21 | -0.54 | 0.927 | 0.994 | 1.000 | 41418 | tags=91%, list=76%, signal=376% | |
5328 | CHLORIDE TRANSPORT | 123 | -0.14 | -0.54 | 0.981 | 0.994 | 1.000 | 21324 | tags=33%, list=39%, signal=53% | |
5329 | PURINE RIBONUCLEOSIDE BISPHOSPHATE BIOSYNTHETIC PROCESS | 13 | -0.20 | -0.54 | 0.938 | 0.994 | 1.000 | 31701 | tags=69%, list=58%, signal=165% | |
5330 | 3'-PHOSPHOADENOSINE 5'-PHOSPHOSULFATE BIOSYNTHETIC PROCESS | 13 | -0.20 | -0.54 | 0.938 | 0.994 | 1.000 | 31701 | tags=69%, list=58%, signal=165% | |
5331 | CALCIUM ION TRANSPORT | 355 | -0.12 | -0.54 | 0.986 | 0.994 | 1.000 | 29350 | tags=42%, list=54%, signal=91% | |
5332 | NEGATIVE REGULATION OF RESPONSE TO WOUNDING | 196 | -0.14 | -0.54 | 0.981 | 0.994 | 1.000 | 35391 | tags=59%, list=65%, signal=167% | |
5333 | REGULATION OF POSITIVE CHEMOTAXIS | 29 | -0.16 | -0.54 | 0.959 | 0.994 | 1.000 | 4368 | tags=10%, list=8%, signal=11% | |
5334 | POSITIVE REGULATION OF PROTEIN GLYCOSYLATION | 11 | -0.23 | -0.54 | 0.941 | 0.994 | 1.000 | 42268 | tags=100%, list=77%, signal=441% | |
5335 | PROSTANOID METABOLIC PROCESS | 49 | -0.16 | -0.54 | 0.979 | 0.994 | 1.000 | 41125 | tags=80%, list=75%, signal=321% | |
5336 | PROSTAGLANDIN METABOLIC PROCESS | 49 | -0.16 | -0.54 | 0.979 | 0.994 | 1.000 | 41125 | tags=80%, list=75%, signal=321% | |
5337 | PHENOL-CONTAINING COMPOUND METABOLIC PROCESS | 72 | -0.14 | -0.54 | 0.994 | 0.994 | 1.000 | 38484 | tags=67%, list=70%, signal=225% | |
5338 | REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 106 | -0.14 | -0.54 | 0.989 | 0.994 | 1.000 | 36113 | tags=62%, list=66%, signal=183% | |
5339 | REGULATION OF SPROUTING ANGIOGENESIS | 58 | -0.15 | -0.54 | 0.989 | 0.994 | 1.000 | 37015 | tags=66%, list=68%, signal=203% | |
5340 | NEURONAL ION CHANNEL CLUSTERING | 23 | -0.18 | -0.54 | 0.975 | 0.994 | 1.000 | 7304 | tags=13%, list=13%, signal=15% | |
5341 | CARDIAC CONDUCTION | 286 | -0.12 | -0.54 | 0.984 | 0.994 | 1.000 | 23366 | tags=33%, list=43%, signal=56% | |
5342 | REGULATION OF SYNAPTIC TRANSMISSION, DOPAMINERGIC | 29 | -0.17 | -0.54 | 0.954 | 0.994 | 1.000 | 14129 | tags=24%, list=26%, signal=33% | |
5343 | PHOTORECEPTOR CELL DIFFERENTIATION | 53 | -0.15 | -0.54 | 0.980 | 0.994 | 1.000 | 11296 | tags=19%, list=21%, signal=24% | |
5344 | MAINTENANCE OF GASTROINTESTINAL EPITHELIUM | 22 | -0.19 | -0.54 | 0.952 | 0.994 | 1.000 | 21072 | tags=41%, list=39%, signal=67% | |
5345 | REGULATION OF INTERLEUKIN-17 PRODUCTION | 31 | -0.19 | -0.54 | 0.927 | 0.994 | 1.000 | 32089 | tags=58%, list=59%, signal=140% | |
5346 | POSITIVE REGULATION OF PROTEIN PROCESSING | 27 | -0.16 | -0.54 | 0.975 | 0.994 | 1.000 | 19577 | tags=33%, list=36%, signal=52% | |
5347 | DETECTION OF MOLECULE OF BACTERIAL ORIGIN | 21 | -0.22 | -0.54 | 0.970 | 0.994 | 1.000 | 41585 | tags=86%, list=76%, signal=358% | |
5348 | NEGATIVE REGULATION OF CELL MIGRATION INVOLVED IN SPROUTING ANGIOGENESIS | 25 | -0.17 | -0.54 | 0.952 | 0.994 | 1.000 | 37015 | tags=68%, list=68%, signal=210% | |
5349 | CAMERA-TYPE EYE MORPHOGENESIS | 106 | -0.13 | -0.54 | 0.992 | 0.994 | 1.000 | 28397 | tags=45%, list=52%, signal=94% | |
5350 | RESPONSE TO HEPARIN | 13 | -0.22 | -0.54 | 0.927 | 0.994 | 1.000 | 40098 | tags=85%, list=73%, signal=317% | |
5351 | REGULATION OF TRANSMEMBRANE TRANSPORT | 680 | -0.12 | -0.54 | 0.998 | 0.994 | 1.000 | 22100 | tags=32%, list=40%, signal=53% | |
5352 | MESODERMAL CELL DIFFERENTIATION | 53 | -0.15 | -0.54 | 0.989 | 0.994 | 1.000 | 35599 | tags=64%, list=65%, signal=184% | |
5353 | POSITIVE REGULATION OF TRANSMEMBRANE TRANSPORT | 198 | -0.13 | -0.54 | 1.000 | 0.994 | 1.000 | 21224 | tags=34%, list=39%, signal=55% | |
5354 | HISTONE H3-K4 TRIMETHYLATION | 33 | -0.19 | -0.54 | 0.941 | 0.994 | 1.000 | 38568 | tags=73%, list=71%, signal=247% | |
5355 | BRANCHING MORPHOGENESIS OF AN EPITHELIAL TUBE | 99 | -0.13 | -0.54 | 0.971 | 0.994 | 1.000 | 28154 | tags=42%, list=51%, signal=87% | |
5356 | CARDIOCYTE DIFFERENTIATION | 150 | -0.13 | -0.54 | 0.996 | 0.994 | 1.000 | 36275 | tags=60%, list=66%, signal=178% | |
5357 | PYRIMIDINE RIBONUCLEOSIDE CATABOLIC PROCESS | 15 | -0.20 | -0.54 | 0.967 | 0.994 | 1.000 | 2095 | tags=13%, list=4%, signal=14% | |
5358 | RESPONSE TO YEAST | 12 | -0.21 | -0.54 | 0.948 | 0.994 | 1.000 | 31832 | tags=50%, list=58%, signal=120% | |
5359 | MUSCLE CELL DEVELOPMENT | 157 | -0.13 | -0.54 | 0.996 | 0.994 | 1.000 | 32590 | tags=55%, list=60%, signal=135% | |
5360 | POSITIVE REGULATION OF WOUND HEALING | 83 | -0.15 | -0.54 | 0.971 | 0.994 | 1.000 | 6770 | tags=13%, list=12%, signal=15% | |
5361 | REGULATION OF LEUKOCYTE PROLIFERATION | 273 | -0.14 | -0.54 | 0.989 | 0.994 | 1.000 | 22653 | tags=35%, list=41%, signal=59% | |
5362 | REGULATION OF LYMPHOCYTE PROLIFERATION | 263 | -0.14 | -0.54 | 0.994 | 0.994 | 1.000 | 22653 | tags=35%, list=41%, signal=59% | |
5363 | COLUMNAR/CUBOIDAL EPITHELIAL CELL DEVELOPMENT | 25 | -0.17 | -0.54 | 0.966 | 0.994 | 1.000 | 32479 | tags=60%, list=59%, signal=148% | |
5364 | CARDIAC LEFT VENTRICLE MORPHOGENESIS | 24 | -0.18 | -0.54 | 0.967 | 0.994 | 1.000 | 8968 | tags=17%, list=16%, signal=20% | |
5365 | HEMATOPOIETIC STEM CELL DIFFERENTIATION | 8 | -0.25 | -0.54 | 0.958 | 0.994 | 1.000 | 37825 | tags=75%, list=69%, signal=243% | |
5366 | POSITIVE REGULATION OF NF-KAPPAB IMPORT INTO NUCLEUS | 26 | -0.23 | -0.54 | 0.928 | 0.994 | 1.000 | 3696 | tags=15%, list=7%, signal=16% | |
5367 | POSITIVE REGULATION OF CELL CYCLE G1/S PHASE TRANSITION | 47 | -0.16 | -0.54 | 0.994 | 0.994 | 1.000 | 42531 | tags=85%, list=78%, signal=383% | |
5368 | NEGATIVE REGULATION OF MYELOID LEUKOCYTE DIFFERENTIATION | 65 | -0.16 | -0.54 | 0.943 | 0.994 | 1.000 | 29594 | tags=45%, list=54%, signal=97% | |
5369 | RECIPROCAL MEIOTIC RECOMBINATION | 44 | -0.15 | -0.54 | 0.973 | 0.994 | 1.000 | 3691 | tags=9%, list=7%, signal=10% | |
5370 | RECIPROCAL DNA RECOMBINATION | 44 | -0.15 | -0.54 | 0.973 | 0.993 | 1.000 | 3691 | tags=9%, list=7%, signal=10% | |
5371 | REGULATION OF SYNAPTIC TRANSMISSION, GLUTAMATERGIC | 44 | -0.16 | -0.53 | 0.960 | 0.994 | 1.000 | 34863 | tags=61%, list=64%, signal=169% | |
5372 | SPINAL CORD DORSAL/VENTRAL PATTERNING | 13 | -0.20 | -0.53 | 0.967 | 0.993 | 1.000 | 38393 | tags=85%, list=70%, signal=284% | |
5373 | OXYGEN HOMEOSTASIS | 13 | -0.25 | -0.53 | 0.906 | 0.994 | 1.000 | 3934 | tags=15%, list=7%, signal=17% | |
5374 | NEGATIVE REGULATION OF PLATELET-DERIVED GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 24 | -0.17 | -0.53 | 0.971 | 0.994 | 1.000 | 29650 | tags=50%, list=54%, signal=109% | |
5375 | DERMATAN SULFATE BIOSYNTHETIC PROCESS | 34 | -0.17 | -0.53 | 0.948 | 0.994 | 1.000 | 37972 | tags=71%, list=69%, signal=231% | |
5376 | REGULATION OF OSTEOBLAST DIFFERENTIATION | 156 | -0.14 | -0.53 | 1.000 | 0.994 | 1.000 | 30878 | tags=48%, list=56%, signal=110% | |
5377 | MULTI-MULTICELLULAR ORGANISM PROCESS | 124 | -0.13 | -0.53 | 0.986 | 0.994 | 1.000 | 28721 | tags=43%, list=53%, signal=90% | |
5378 | CELL MIGRATION INVOLVED IN HEART DEVELOPMENT | 13 | -0.20 | -0.53 | 0.965 | 0.994 | 1.000 | 35819 | tags=69%, list=66%, signal=201% | |
5379 | CAMP-MEDIATED SIGNALING | 46 | -0.15 | -0.53 | 0.976 | 0.994 | 1.000 | 8382 | tags=13%, list=15%, signal=15% | |
5380 | DRUG METABOLIC PROCESS | 70 | -0.14 | -0.53 | 0.969 | 0.994 | 1.000 | 32699 | tags=60%, list=60%, signal=149% | |
5381 | NEGATIVE REGULATION BY HOST OF VIRAL TRANSCRIPTION | 31 | -0.18 | -0.53 | 0.979 | 0.994 | 1.000 | 40469 | tags=81%, list=74%, signal=310% | |
5382 | POSITIVE REGULATION OF CYTOSOLIC CALCIUM ION CONCENTRATION INVOLVED IN PHOSPHOLIPASE C-ACTIVATING G-PROTEIN COUPLED SIGNALING PATHWAY | 21 | -0.17 | -0.53 | 0.944 | 0.994 | 1.000 | 36712 | tags=62%, list=67%, signal=188% | |
5383 | REGULATION OF MONONUCLEAR CELL PROLIFERATION | 267 | -0.14 | -0.53 | 0.992 | 0.994 | 1.000 | 22653 | tags=34%, list=41%, signal=59% | |
5384 | REGULATION OF DENDRITIC CELL ANTIGEN PROCESSING AND PRESENTATION | 19 | -0.19 | -0.53 | 0.926 | 0.994 | 1.000 | 5047 | tags=16%, list=9%, signal=17% | |
5385 | PROTEIN GERANYLGERANYLATION | 19 | -0.19 | -0.53 | 0.941 | 0.994 | 1.000 | 41580 | tags=84%, list=76%, signal=351% | |
5386 | STRIATED MUSCLE CELL DIFFERENTIATION | 192 | -0.13 | -0.53 | 0.991 | 0.994 | 1.000 | 35531 | tags=61%, list=65%, signal=173% | |
5387 | DIENCEPHALON DEVELOPMENT | 40 | -0.16 | -0.53 | 0.971 | 0.994 | 1.000 | 37910 | tags=70%, list=69%, signal=228% | |
5388 | REGULATION OF ALDOSTERONE METABOLIC PROCESS | 17 | -0.19 | -0.53 | 0.969 | 0.994 | 1.000 | 39265 | tags=71%, list=72%, signal=250% | |
5389 | REGULATION OF ALDOSTERONE BIOSYNTHETIC PROCESS | 17 | -0.19 | -0.53 | 0.969 | 0.994 | 1.000 | 39265 | tags=71%, list=72%, signal=250% | |
5390 | REGULATION OF STEROID HORMONE BIOSYNTHETIC PROCESS | 17 | -0.19 | -0.53 | 0.969 | 0.994 | 1.000 | 39265 | tags=71%, list=72%, signal=250% | |
5391 | NEUROTRANSMITTER UPTAKE | 18 | -0.19 | -0.53 | 0.974 | 0.994 | 1.000 | 38110 | tags=78%, list=70%, signal=257% | |
5392 | MAST CELL MEDIATED IMMUNITY | 18 | -0.21 | -0.53 | 0.931 | 0.995 | 1.000 | 20653 | tags=39%, list=38%, signal=62% | |
5393 | NEGATIVE REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR SIGNALING PATHWAY | 13 | -0.22 | -0.53 | 0.940 | 0.995 | 1.000 | 5175 | tags=15%, list=9%, signal=17% | |
5394 | WOUND HEALING, SPREADING OF EPIDERMAL CELLS | 12 | -0.19 | -0.53 | 0.977 | 0.995 | 1.000 | 7025 | tags=17%, list=13%, signal=19% | |
5395 | NEGATIVE REGULATION OF CYTOKINE SECRETION | 84 | -0.15 | -0.53 | 0.990 | 0.995 | 1.000 | 34534 | tags=56%, list=63%, signal=152% | |
5396 | POSITIVE REGULATION OF CYCLIC NUCLEOTIDE BIOSYNTHETIC PROCESS | 140 | -0.13 | -0.53 | 0.983 | 0.995 | 1.000 | 30167 | tags=44%, list=55%, signal=97% | |
5397 | RETINA MORPHOGENESIS IN CAMERA-TYPE EYE | 53 | -0.14 | -0.53 | 0.977 | 0.995 | 1.000 | 25497 | tags=42%, list=47%, signal=78% | |
5398 | REGULATION OF VITAMIN METABOLIC PROCESS | 14 | -0.22 | -0.53 | 0.963 | 0.996 | 1.000 | 14790 | tags=29%, list=27%, signal=39% | |
5399 | PROTEIN LOCALIZATION TO CYTOPLASMIC STRESS GRANULE | 24 | -0.20 | -0.53 | 0.893 | 0.996 | 1.000 | 9881 | tags=21%, list=18%, signal=25% | |
5400 | BASEMENT MEMBRANE ORGANIZATION | 14 | -0.20 | -0.53 | 0.956 | 0.996 | 1.000 | 20223 | tags=36%, list=37%, signal=57% | |
5401 | POSITIVE REGULATION OF RESPONSE TO WOUNDING | 160 | -0.15 | -0.52 | 0.972 | 0.996 | 1.000 | 37049 | tags=64%, list=68%, signal=199% | |
5402 | CELL-CELL SIGNALING INVOLVED IN CARDIAC CONDUCTION | 34 | -0.15 | -0.52 | 0.982 | 0.996 | 1.000 | 25209 | tags=35%, list=46%, signal=65% | |
5403 | REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 69 | -0.14 | -0.52 | 0.973 | 0.996 | 1.000 | 32216 | tags=49%, list=59%, signal=120% | |
5404 | NEGATIVE REGULATION OF FERTILIZATION | 4 | -0.29 | -0.52 | 0.970 | 0.996 | 1.000 | 33714 | tags=75%, list=62%, signal=196% | |
5405 | NEGATIVE REGULATION OF REGULATED SECRETORY PATHWAY | 19 | -0.18 | -0.52 | 0.960 | 0.996 | 1.000 | 11234 | tags=21%, list=21%, signal=26% | |
5406 | POST-EMBRYONIC ORGAN DEVELOPMENT | 13 | -0.21 | -0.52 | 0.925 | 0.996 | 1.000 | 27706 | tags=54%, list=51%, signal=109% | |
5407 | RENAL ABSORPTION | 23 | -0.19 | -0.52 | 0.968 | 0.996 | 1.000 | 41785 | tags=83%, list=76%, signal=350% | |
5408 | REGULATION OF CATION TRANSMEMBRANE TRANSPORT | 362 | -0.12 | -0.52 | 1.000 | 0.996 | 1.000 | 21623 | tags=32%, list=40%, signal=53% | |
5409 | PEPTIDYL-CYSTEINE MODIFICATION | 39 | -0.15 | -0.52 | 0.992 | 0.996 | 1.000 | 20588 | tags=36%, list=38%, signal=58% | |
5410 | MESENCHYMAL CELL PROLIFERATION | 26 | -0.17 | -0.52 | 0.952 | 0.996 | 1.000 | 35335 | tags=62%, list=65%, signal=174% | |
5411 | SINGLE-ORGANISM BEHAVIOR | 259 | -0.12 | -0.52 | 0.992 | 0.996 | 1.000 | 21892 | tags=31%, list=40%, signal=52% | |
5412 | POSITIVE CHEMOTAXIS | 65 | -0.14 | -0.52 | 0.998 | 0.996 | 1.000 | 28783 | tags=45%, list=53%, signal=94% | |
5413 | IMMUNE RESPONSE-INHIBITING SIGNAL TRANSDUCTION | 13 | -0.24 | -0.52 | 0.945 | 0.996 | 1.000 | 26401 | tags=54%, list=48%, signal=104% | |
5414 | IMMUNE RESPONSE-INHIBITING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 13 | -0.24 | -0.52 | 0.945 | 0.995 | 1.000 | 26401 | tags=54%, list=48%, signal=104% | |
5415 | POSITIVE REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 33 | -0.16 | -0.52 | 0.938 | 0.996 | 1.000 | 35029 | tags=61%, list=64%, signal=169% | |
5416 | CELLULAR RESPONSE TO HEPARIN | 12 | -0.22 | -0.52 | 0.951 | 0.995 | 1.000 | 40098 | tags=92%, list=73%, signal=344% | |
5417 | NEGATIVE REGULATION OF MONONUCLEAR CELL PROLIFERATION | 74 | -0.16 | -0.52 | 0.961 | 0.995 | 1.000 | 24197 | tags=38%, list=44%, signal=68% | |
5418 | NEGATIVE REGULATION OF LYMPHOCYTE PROLIFERATION | 74 | -0.16 | -0.52 | 0.961 | 0.995 | 1.000 | 24197 | tags=38%, list=44%, signal=68% | |
5419 | POSITIVE REGULATION OF LEUKOCYTE PROLIFERATION | 184 | -0.14 | -0.52 | 0.985 | 0.996 | 1.000 | 28332 | tags=44%, list=52%, signal=91% | |
5420 | POSITIVE REGULATION OF CELLULAR EXTRAVASATION | 9 | -0.27 | -0.52 | 0.975 | 0.996 | 1.000 | 25252 | tags=56%, list=46%, signal=103% | |
5421 | REGULATION OF BLOOD PRESSURE | 174 | -0.13 | -0.52 | 0.982 | 0.996 | 1.000 | 34457 | tags=55%, list=63%, signal=149% | |
5422 | ESTROGEN BIOSYNTHETIC PROCESS | 12 | -0.20 | -0.52 | 0.957 | 0.996 | 1.000 | 40601 | tags=83%, list=74%, signal=324% | |
5423 | POSITIVE REGULATION OF B CELL PROLIFERATION | 58 | -0.15 | -0.52 | 0.978 | 0.996 | 1.000 | 29243 | tags=45%, list=53%, signal=96% | |
5424 | REGULATION OF ION TRANSMEMBRANE TRANSPORT | 658 | -0.11 | -0.52 | 1.000 | 0.996 | 1.000 | 22100 | tags=32%, list=40%, signal=53% | |
5425 | POSITIVE REGULATION OF LYMPHOCYTE PROLIFERATION | 177 | -0.14 | -0.52 | 0.994 | 0.996 | 1.000 | 21084 | tags=32%, list=39%, signal=52% | |
5426 | ONCOSTATIN-M-MEDIATED SIGNALING PATHWAY | 17 | -0.20 | -0.52 | 0.950 | 0.996 | 1.000 | 4822 | tags=12%, list=9%, signal=13% | |
5427 | POSITIVE REGULATION OF NEUROBLAST PROLIFERATION | 25 | -0.17 | -0.52 | 0.947 | 0.996 | 1.000 | 37853 | tags=72%, list=69%, signal=234% | |
5428 | REGULATION OF MEMBRANE DEPOLARIZATION | 64 | -0.14 | -0.52 | 0.986 | 0.996 | 1.000 | 39596 | tags=70%, list=72%, signal=255% | |
5429 | MUSCLE CELL DIFFERENTIATION | 351 | -0.12 | -0.52 | 0.998 | 0.996 | 1.000 | 32216 | tags=52%, list=59%, signal=125% | |
5430 | ADAPTIVE IMMUNE RESPONSE BASED ON SOMATIC RECOMBINATION OF IMMUNE RECEPTORS BUILT FROM IMMUNOGLOBULIN SUPERFAMILY DOMAINS | 199 | -0.13 | -0.52 | 0.990 | 0.996 | 1.000 | 27979 | tags=42%, list=51%, signal=85% | |
5431 | REGULATION OF CARTILAGE DEVELOPMENT | 71 | -0.13 | -0.52 | 0.988 | 0.996 | 1.000 | 33764 | tags=55%, list=62%, signal=143% | |
5432 | NEGATIVE REGULATION OF INTERLEUKIN-10 PRODUCTION | 25 | -0.17 | -0.52 | 0.965 | 0.996 | 1.000 | 25520 | tags=40%, list=47%, signal=75% | |
5433 | CARDIAC MUSCLE CELL DIFFERENTIATION | 111 | -0.13 | -0.52 | 0.992 | 0.996 | 1.000 | 35400 | tags=59%, list=65%, signal=168% | |
5434 | POSITIVE REGULATION OF MONONUCLEAR CELL PROLIFERATION | 181 | -0.13 | -0.52 | 0.992 | 0.996 | 1.000 | 21084 | tags=32%, list=39%, signal=52% | |
5435 | OLIGOPEPTIDE TRANSPORT | 5 | -0.26 | -0.52 | 0.982 | 0.997 | 1.000 | 16820 | tags=40%, list=31%, signal=58% | |
5436 | INORGANIC ANION TRANSPORT | 178 | -0.13 | -0.51 | 0.998 | 0.997 | 1.000 | 24828 | tags=38%, list=45%, signal=69% | |
5437 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT PROTEIN | 86 | -0.14 | -0.51 | 0.983 | 0.998 | 1.000 | 28332 | tags=42%, list=52%, signal=87% | |
5438 | POSITIVE REGULATION OF G1/S TRANSITION OF MITOTIC CELL CYCLE | 34 | -0.16 | -0.51 | 0.976 | 0.998 | 1.000 | 42531 | tags=85%, list=78%, signal=384% | |
5439 | POSITIVE REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 48 | -0.14 | -0.51 | 0.958 | 0.997 | 1.000 | 28154 | tags=42%, list=51%, signal=86% | |
5440 | AXON EXTENSION INVOLVED IN AXON GUIDANCE | 31 | -0.15 | -0.51 | 0.949 | 0.997 | 1.000 | 40112 | tags=74%, list=73%, signal=278% | |
5441 | NEURON PROJECTION EXTENSION INVOLVED IN NEURON PROJECTION GUIDANCE | 31 | -0.15 | -0.51 | 0.949 | 0.997 | 1.000 | 40112 | tags=74%, list=73%, signal=278% | |
5442 | NEGATIVE REGULATION OF SMOOTH MUSCLE CELL MIGRATION | 35 | -0.15 | -0.51 | 0.979 | 0.997 | 1.000 | 25005 | tags=40%, list=46%, signal=74% | |
5443 | ORNITHINE METABOLIC PROCESS | 10 | -0.23 | -0.51 | 0.981 | 0.997 | 1.000 | 16333 | tags=30%, list=30%, signal=43% | |
5444 | CILIUM OR FLAGELLUM-DEPENDENT CELL MOTILITY | 7 | -0.27 | -0.51 | 0.953 | 0.997 | 1.000 | 40092 | tags=100%, list=73%, signal=375% | |
5445 | CILIUM-DEPENDENT CELL MOTILITY | 7 | -0.27 | -0.51 | 0.953 | 0.997 | 1.000 | 40092 | tags=100%, list=73%, signal=375% | |
5446 | CELL CHEMOTAXIS | 231 | -0.14 | -0.51 | 0.981 | 0.997 | 1.000 | 25307 | tags=38%, list=46%, signal=71% | |
5447 | MESENCHYME MORPHOGENESIS | 39 | -0.15 | -0.51 | 0.967 | 0.997 | 1.000 | 27150 | tags=44%, list=50%, signal=87% | |
5448 | CYCLIC-NUCLEOTIDE-MEDIATED SIGNALING | 65 | -0.14 | -0.51 | 0.998 | 0.997 | 1.000 | 35476 | tags=54%, list=65%, signal=153% | |
5449 | REGULATION OF PLATELET ACTIVATION | 54 | -0.16 | -0.51 | 0.960 | 0.997 | 1.000 | 27471 | tags=44%, list=50%, signal=89% | |
5450 | REGULATION OF SMOOTH MUSCLE CONTRACTION | 42 | -0.16 | -0.51 | 0.965 | 0.997 | 1.000 | 14060 | tags=24%, list=26%, signal=32% | |
5451 | NEGATIVE REGULATION OF BONE MINERALIZATION | 18 | -0.20 | -0.51 | 0.963 | 0.997 | 1.000 | 36642 | tags=72%, list=67%, signal=219% | |
5452 | T CELL SELECTION | 27 | -0.19 | -0.51 | 0.946 | 0.997 | 1.000 | 16174 | tags=30%, list=30%, signal=42% | |
5453 | CYTOKINE BIOSYNTHETIC PROCESS | 14 | -0.19 | -0.51 | 0.979 | 0.997 | 1.000 | 33453 | tags=64%, list=61%, signal=166% | |
5454 | NEGATIVE REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 39 | -0.16 | -0.51 | 0.974 | 0.997 | 1.000 | 41802 | tags=77%, list=76%, signal=326% | |
5455 | SECONDARY METABOLIC PROCESS | 49 | -0.15 | -0.51 | 0.973 | 0.998 | 1.000 | 41512 | tags=80%, list=76%, signal=330% | |
5456 | NEPHRON DEVELOPMENT | 166 | -0.13 | -0.51 | 0.987 | 0.998 | 1.000 | 33362 | tags=52%, list=61%, signal=134% | |
5457 | POSITIVE REGULATION OF T CELL CHEMOTAXIS | 19 | -0.19 | -0.51 | 0.957 | 0.998 | 1.000 | 40129 | tags=79%, list=73%, signal=297% | |
5458 | EYE MORPHOGENESIS | 148 | -0.12 | -0.51 | 1.000 | 0.998 | 1.000 | 30327 | tags=48%, list=55%, signal=107% | |
5459 | RESPONSE TO PAIN | 15 | -0.20 | -0.51 | 0.954 | 0.998 | 1.000 | 36089 | tags=73%, list=66%, signal=216% | |
5460 | NEGATIVE REGULATION OF RESPONSE TO CYTOKINE STIMULUS | 81 | -0.15 | -0.51 | 0.989 | 0.998 | 1.000 | 20589 | tags=30%, list=38%, signal=47% | |
5461 | NEUROMUSCULAR PROCESS | 64 | -0.14 | -0.51 | 0.991 | 0.998 | 1.000 | 18940 | tags=30%, list=35%, signal=45% | |
5462 | T-HELPER CELL LINEAGE COMMITMENT | 9 | -0.24 | -0.51 | 0.937 | 0.998 | 1.000 | 31167 | tags=67%, list=57%, signal=155% | |
5463 | T-HELPER 17 CELL LINEAGE COMMITMENT | 9 | -0.24 | -0.51 | 0.937 | 0.998 | 1.000 | 31167 | tags=67%, list=57%, signal=155% | |
5464 | REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS | 51 | -0.15 | -0.51 | 0.973 | 0.998 | 1.000 | 35225 | tags=59%, list=64%, signal=165% | |
5465 | ARACHIDONIC ACID SECRETION | 15 | -0.18 | -0.51 | 0.979 | 0.998 | 1.000 | 28417 | tags=53%, list=52%, signal=111% | |
5466 | ARACHIDONATE TRANSPORT | 15 | -0.18 | -0.51 | 0.979 | 0.998 | 1.000 | 28417 | tags=53%, list=52%, signal=111% | |
5467 | POSITIVE REGULATION OF MYELOID LEUKOCYTE CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 14 | -0.19 | -0.50 | 0.975 | 0.998 | 1.000 | 40510 | tags=79%, list=74%, signal=303% | |
5468 | ENDOTHELIAL CELL PROLIFERATION | 41 | -0.13 | -0.50 | 0.974 | 0.998 | 1.000 | 38306 | tags=68%, list=70%, signal=228% | |
5469 | CAMP CATABOLIC PROCESS | 23 | -0.17 | -0.50 | 0.988 | 0.998 | 1.000 | 28323 | tags=43%, list=52%, signal=90% | |
5470 | CHOLESTEROL CATABOLIC PROCESS | 6 | -0.26 | -0.50 | 0.972 | 0.998 | 1.000 | 36008 | tags=83%, list=66%, signal=244% | |
5471 | STEROL CATABOLIC PROCESS | 6 | -0.26 | -0.50 | 0.972 | 0.998 | 1.000 | 36008 | tags=83%, list=66%, signal=244% | |
5472 | POSITIVE REGULATION OF SODIUM ION TRANSMEMBRANE TRANSPORT | 41 | -0.13 | -0.50 | 0.987 | 0.998 | 1.000 | 25853 | tags=46%, list=47%, signal=88% | |
5473 | SODIUM-INDEPENDENT ORGANIC ANION TRANSPORT | 28 | -0.16 | -0.50 | 0.978 | 0.999 | 1.000 | 38634 | tags=71%, list=71%, signal=243% | |
5474 | REGULATION OF POTASSIUM ION TRANSMEMBRANE TRANSPORT | 114 | -0.12 | -0.50 | 0.998 | 0.999 | 1.000 | 15979 | tags=24%, list=29%, signal=33% | |
5475 | REGULATION OF T CELL CHEMOTAXIS | 20 | -0.19 | -0.50 | 0.971 | 0.999 | 1.000 | 40326 | tags=80%, list=74%, signal=305% | |
5476 | SENSORY PERCEPTION OF CHEMICAL STIMULUS | 96 | -0.13 | -0.50 | 0.984 | 0.999 | 1.000 | 34649 | tags=54%, list=63%, signal=148% | |
5477 | POSITIVE REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 43 | -0.15 | -0.50 | 0.975 | 0.999 | 1.000 | 9002 | tags=16%, list=16%, signal=19% | |
5478 | REGULATION OF NUCLEOTIDE BIOSYNTHETIC PROCESS | 195 | -0.12 | -0.50 | 0.984 | 0.999 | 1.000 | 30167 | tags=43%, list=55%, signal=95% | |
5479 | REGULATION OF PURINE NUCLEOTIDE BIOSYNTHETIC PROCESS | 195 | -0.12 | -0.50 | 0.984 | 0.998 | 1.000 | 30167 | tags=43%, list=55%, signal=95% | |
5480 | DENDRITIC CELL CHEMOTAXIS | 25 | -0.19 | -0.50 | 0.947 | 0.999 | 1.000 | 25252 | tags=44%, list=46%, signal=82% | |
5481 | REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 47 | -0.14 | -0.50 | 0.968 | 0.999 | 1.000 | 28154 | tags=43%, list=51%, signal=88% | |
5482 | EPIDERMIS MORPHOGENESIS | 27 | -0.17 | -0.50 | 0.957 | 0.999 | 1.000 | 15881 | tags=30%, list=29%, signal=42% | |
5483 | REGULATION OF HEART GROWTH | 58 | -0.14 | -0.50 | 0.978 | 0.999 | 1.000 | 31828 | tags=48%, list=58%, signal=115% | |
5484 | REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL PROLIFERATION INVOLVED IN SPROUTING ANGIOGENESIS | 5 | -0.25 | -0.50 | 0.981 | 0.999 | 1.000 | 15640 | tags=40%, list=29%, signal=56% | |
5485 | POSITIVE REGULATION OF T CELL PROLIFERATION | 124 | -0.14 | -0.50 | 0.994 | 0.999 | 1.000 | 19703 | tags=31%, list=36%, signal=48% | |
5486 | EPITHELIAL CELL APOPTOTIC PROCESS | 31 | -0.16 | -0.50 | 0.969 | 1.000 | 1.000 | 42212 | tags=77%, list=77%, signal=339% | |
5487 | POSITIVE REGULATION OF ION TRANSMEMBRANE TRANSPORT | 191 | -0.12 | -0.50 | 1.000 | 1.000 | 1.000 | 21224 | tags=33%, list=39%, signal=54% | |
5488 | VISUAL BEHAVIOR | 40 | -0.14 | -0.50 | 0.975 | 1.000 | 1.000 | 1704 | tags=8%, list=3%, signal=8% | |
5489 | CELL DIFFERENTIATION IN SPINAL CORD | 31 | -0.15 | -0.50 | 0.978 | 1.000 | 1.000 | 32149 | tags=55%, list=59%, signal=133% | |
5490 | REGULATION OF CHOLESTEROL HOMEOSTASIS | 33 | -0.13 | -0.49 | 0.990 | 1.000 | 1.000 | 4567 | tags=9%, list=8%, signal=10% | |
5491 | REGULATION OF SODIUM ION TRANSMEMBRANE TRANSPORT | 92 | -0.12 | -0.49 | 0.998 | 1.000 | 1.000 | 26088 | tags=42%, list=48%, signal=81% | |
5492 | ENDOTHELIAL CELL CHEMOTAXIS | 20 | -0.18 | -0.49 | 0.954 | 1.000 | 1.000 | 16728 | tags=25%, list=31%, signal=36% | |
5493 | REGULATION OF T CELL MIGRATION | 35 | -0.17 | -0.49 | 0.982 | 1.000 | 1.000 | 41802 | tags=80%, list=76%, signal=340% | |
5494 | REGULATION OF CAMP METABOLIC PROCESS | 181 | -0.12 | -0.49 | 0.987 | 1.000 | 1.000 | 30167 | tags=43%, list=55%, signal=95% | |
5495 | CYTOSOLIC CALCIUM ION TRANSPORT | 107 | -0.12 | -0.49 | 0.982 | 1.000 | 1.000 | 29350 | tags=44%, list=54%, signal=95% | |
5496 | NEGATIVE CHEMOTAXIS | 37 | -0.15 | -0.49 | 0.966 | 1.000 | 1.000 | 40112 | tags=73%, list=73%, signal=274% | |
5497 | POSITIVE REGULATION OF MITOTIC CELL CYCLE SPINDLE ASSEMBLY CHECKPOINT | 14 | -0.20 | -0.49 | 0.961 | 1.000 | 1.000 | 31967 | tags=64%, list=58%, signal=155% | |
5498 | CELL MATURATION | 76 | -0.12 | -0.49 | 0.992 | 1.000 | 1.000 | 21387 | tags=29%, list=39%, signal=47% | |
5499 | POSITIVE REGULATION OF CARDIAC MUSCLE HYPERTROPHY | 42 | -0.15 | -0.49 | 0.983 | 1.000 | 1.000 | 39062 | tags=69%, list=71%, signal=242% | |
5500 | POSITIVE REGULATION OF MUSCLE HYPERTROPHY | 42 | -0.15 | -0.49 | 0.983 | 1.000 | 1.000 | 39062 | tags=69%, list=71%, signal=242% | |
5501 | SYNAPSE ORGANIZATION | 159 | -0.12 | -0.49 | 0.986 | 1.000 | 1.000 | 20135 | tags=30%, list=37%, signal=47% | |
5502 | SOCIAL BEHAVIOR | 71 | -0.13 | -0.49 | 0.985 | 1.000 | 1.000 | 18246 | tags=30%, list=33%, signal=44% | |
5503 | INTRASPECIES INTERACTION BETWEEN ORGANISMS | 71 | -0.13 | -0.49 | 0.985 | 1.000 | 1.000 | 18246 | tags=30%, list=33%, signal=44% | |
5504 | POSITIVE REGULATION OF INFLAMMATORY RESPONSE | 80 | -0.16 | -0.49 | 0.992 | 1.000 | 1.000 | 36972 | tags=65%, list=68%, signal=200% | |
5505 | FEEDING BEHAVIOR | 49 | -0.13 | -0.49 | 0.986 | 1.000 | 1.000 | 23967 | tags=33%, list=44%, signal=58% | |
5506 | RESPONSE TO GONADOTROPIN | 18 | -0.17 | -0.49 | 0.992 | 1.000 | 1.000 | 6855 | tags=17%, list=13%, signal=19% | |
5507 | AV NODE CELL TO BUNDLE OF HIS CELL COMMUNICATION | 9 | -0.20 | -0.49 | 0.978 | 1.000 | 1.000 | 35400 | tags=67%, list=65%, signal=189% | |
5508 | REGULATION OF VOLTAGE-GATED CALCIUM CHANNEL ACTIVITY | 31 | -0.15 | -0.49 | 0.992 | 1.000 | 1.000 | 29434 | tags=45%, list=54%, signal=98% | |
5509 | REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE | 109 | -0.13 | -0.49 | 0.990 | 1.000 | 1.000 | 38370 | tags=63%, list=70%, signal=212% | |
5510 | NEGATIVE REGULATION OF LIPASE ACTIVITY | 34 | -0.15 | -0.49 | 0.985 | 1.000 | 1.000 | 33046 | tags=53%, list=60%, signal=134% | |
5511 | POSITIVE REGULATION OF MRNA SPLICING, VIA SPLICEOSOME | 21 | -0.15 | -0.49 | 0.996 | 1.000 | 1.000 | 20978 | tags=33%, list=38%, signal=54% | |
5512 | EXTRACELLULAR FIBRIL ORGANIZATION | 26 | -0.16 | -0.49 | 0.978 | 1.000 | 1.000 | 36946 | tags=69%, list=68%, signal=213% | |
5513 | MEMBRANE DEPOLARIZATION DURING SA NODE CELL ACTION POTENTIAL | 9 | -0.19 | -0.49 | 0.986 | 1.000 | 1.000 | 25209 | tags=44%, list=46%, signal=82% | |
5514 | GAS HOMEOSTASIS | 15 | -0.21 | -0.48 | 0.976 | 1.000 | 1.000 | 3934 | tags=13%, list=7%, signal=14% | |
5515 | REGULATION OF MITOCHONDRIAL DEPOLARIZATION | 24 | -0.16 | -0.48 | 0.974 | 1.000 | 1.000 | 38097 | tags=67%, list=70%, signal=220% | |
5516 | ACTIVATION OF TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE ACTIVITY | 24 | -0.15 | -0.48 | 0.986 | 1.000 | 1.000 | 32216 | tags=54%, list=59%, signal=132% | |
5517 | SENSORY PERCEPTION OF BITTER TASTE | 32 | -0.15 | -0.48 | 0.975 | 1.000 | 1.000 | 31487 | tags=50%, list=58%, signal=118% | |
5518 | MESODERM MORPHOGENESIS | 75 | -0.13 | -0.48 | 0.998 | 1.000 | 1.000 | 37449 | tags=65%, list=68%, signal=207% | |
5519 | MESONEPHROS DEVELOPMENT | 79 | -0.13 | -0.48 | 0.983 | 1.000 | 1.000 | 17093 | tags=24%, list=31%, signal=35% | |
5520 | CARDIAC CELL FATE COMMITMENT | 11 | -0.19 | -0.48 | 0.977 | 1.000 | 1.000 | 35345 | tags=73%, list=65%, signal=206% | |
5521 | ACYLGLYCEROL HOMEOSTASIS | 59 | -0.13 | -0.48 | 0.990 | 1.000 | 1.000 | 2230 | tags=7%, list=4%, signal=7% | |
5522 | TRIGLYCERIDE HOMEOSTASIS | 59 | -0.13 | -0.48 | 0.990 | 1.000 | 1.000 | 2230 | tags=7%, list=4%, signal=7% | |
5523 | DENDRITIC CELL DIFFERENTIATION | 32 | -0.16 | -0.48 | 0.970 | 1.000 | 1.000 | 28163 | tags=47%, list=52%, signal=97% | |
5524 | NEGATIVE REGULATION OF TISSUE REMODELING | 14 | -0.18 | -0.48 | 0.984 | 1.000 | 1.000 | 37825 | tags=64%, list=69%, signal=209% | |
5525 | MESODERM DEVELOPMENT | 126 | -0.12 | -0.48 | 0.996 | 1.000 | 1.000 | 37532 | tags=63%, list=69%, signal=202% | |
5526 | POSITIVE REGULATION OF CARDIAC MUSCLE TISSUE GROWTH | 39 | -0.14 | -0.48 | 0.970 | 1.000 | 1.000 | 28154 | tags=41%, list=51%, signal=85% | |
5527 | EXCRETION | 62 | -0.13 | -0.48 | 0.979 | 1.000 | 1.000 | 25305 | tags=37%, list=46%, signal=69% | |
5528 | NEGATIVE REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 21 | -0.16 | -0.48 | 0.988 | 1.000 | 1.000 | 25734 | tags=43%, list=47%, signal=81% | |
5529 | REGULATION OF PROTEIN LOCALIZATION TO EARLY ENDOSOME | 17 | -0.19 | -0.48 | 0.949 | 1.000 | 1.000 | 35029 | tags=65%, list=64%, signal=180% | |
5530 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO EARLY ENDOSOME | 17 | -0.19 | -0.48 | 0.949 | 1.000 | 1.000 | 35029 | tags=65%, list=64%, signal=180% | |
5531 | AMINO ACID IMPORT | 17 | -0.18 | -0.48 | 0.959 | 1.000 | 1.000 | 33992 | tags=65%, list=62%, signal=171% | |
5532 | PEPTIDE CROSS-LINKING | 31 | -0.18 | -0.48 | 0.960 | 1.000 | 1.000 | 37008 | tags=71%, list=68%, signal=220% | |
5533 | REGULATION OF BLOOD CIRCULATION | 464 | -0.11 | -0.47 | 1.000 | 1.000 | 1.000 | 24523 | tags=34%, list=45%, signal=60% | |
5534 | URETERIC BUD DEVELOPMENT | 71 | -0.13 | -0.47 | 0.984 | 1.000 | 1.000 | 17093 | tags=24%, list=31%, signal=35% | |
5535 | SECRETORY GRANULE ORGANIZATION | 17 | -0.18 | -0.47 | 0.979 | 1.000 | 1.000 | 41896 | tags=88%, list=77%, signal=377% | |
5536 | POSITIVE REGULATION OF CIRCADIAN RHYTHM | 35 | -0.16 | -0.47 | 0.968 | 1.000 | 1.000 | 18639 | tags=29%, list=34%, signal=43% | |
5537 | POSITIVE REGULATION OF OSSIFICATION | 123 | -0.12 | -0.47 | 0.998 | 1.000 | 1.000 | 30361 | tags=45%, list=56%, signal=100% | |
5538 | CGMP-MEDIATED SIGNALING | 17 | -0.17 | -0.47 | 0.989 | 1.000 | 1.000 | 25375 | tags=41%, list=46%, signal=77% | |
5539 | CALCIUM ION TRANSPORT INTO CYTOSOL | 103 | -0.12 | -0.47 | 0.986 | 1.000 | 1.000 | 33408 | tags=51%, list=61%, signal=132% | |
5540 | REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR PRODUCTION | 71 | -0.15 | -0.47 | 0.979 | 1.000 | 1.000 | 37806 | tags=63%, list=69%, signal=205% | |
5541 | CELLULAR RESPONSE TO AMMONIUM ION | 29 | -0.16 | -0.47 | 0.976 | 1.000 | 1.000 | 39845 | tags=72%, list=73%, signal=267% | |
5542 | REGULATION OF LYMPHOCYTE MIGRATION | 55 | -0.15 | -0.47 | 0.988 | 1.000 | 1.000 | 41851 | tags=76%, list=77%, signal=325% | |
5543 | NEPHRON MORPHOGENESIS | 65 | -0.13 | -0.47 | 0.983 | 1.000 | 1.000 | 33971 | tags=51%, list=62%, signal=134% | |
5544 | NEPHRON EPITHELIUM MORPHOGENESIS | 65 | -0.13 | -0.47 | 0.983 | 1.000 | 1.000 | 33971 | tags=51%, list=62%, signal=134% | |
5545 | LENS FIBER CELL DIFFERENTIATION | 14 | -0.18 | -0.47 | 0.978 | 1.000 | 1.000 | 36238 | tags=64%, list=66%, signal=191% | |
5546 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO VASCULAR ENDOTHELIAL GROWTH FACTOR STIMULUS | 15 | -0.19 | -0.47 | 0.966 | 1.000 | 1.000 | 41139 | tags=80%, list=75%, signal=323% | |
5547 | OLIGOSACCHARIDE CATABOLIC PROCESS | 7 | -0.23 | -0.47 | 0.978 | 1.000 | 1.000 | 18661 | tags=29%, list=34%, signal=43% | |
5548 | EYE PHOTORECEPTOR CELL DIFFERENTIATION | 42 | -0.13 | -0.47 | 0.988 | 1.000 | 1.000 | 19109 | tags=29%, list=35%, signal=44% | |
5549 | REGULATION OF T-HELPER 2 CELL CYTOKINE PRODUCTION | 12 | -0.20 | -0.47 | 0.967 | 1.000 | 1.000 | 2006 | tags=8%, list=4%, signal=9% | |
5550 | G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY, COUPLED TO CYCLIC NUCLEOTIDE SECOND MESSENGER | 229 | -0.11 | -0.47 | 0.979 | 1.000 | 1.000 | 20766 | tags=28%, list=38%, signal=45% | |
5551 | DEFENSE RESPONSE TO FUNGUS | 25 | -0.17 | -0.47 | 0.990 | 1.000 | 1.000 | 14617 | tags=24%, list=27%, signal=33% | |
5552 | POSITIVE REGULATION OF ORGAN GROWTH | 46 | -0.13 | -0.47 | 0.982 | 1.000 | 1.000 | 31828 | tags=48%, list=58%, signal=114% | |
5553 | POSITIVE REGULATION OF HEART GROWTH | 46 | -0.13 | -0.47 | 0.982 | 1.000 | 1.000 | 31828 | tags=48%, list=58%, signal=114% | |
5554 | GLOMERULUS DEVELOPMENT | 94 | -0.12 | -0.47 | 0.992 | 1.000 | 1.000 | 36858 | tags=62%, list=67%, signal=189% | |
5555 | KERATINOCYTE DIFFERENTIATION | 57 | -0.14 | -0.47 | 0.975 | 1.000 | 1.000 | 17645 | tags=28%, list=32%, signal=41% | |
5556 | MESENCHYMAL TO EPITHELIAL TRANSITION INVOLVED IN METANEPHROS MORPHOGENESIS | 16 | -0.18 | -0.47 | 0.971 | 1.000 | 1.000 | 32287 | tags=56%, list=59%, signal=137% | |
5557 | METANEPHRIC RENAL VESICLE MORPHOGENESIS | 16 | -0.18 | -0.47 | 0.971 | 1.000 | 1.000 | 32287 | tags=56%, list=59%, signal=137% | |
5558 | NEGATIVE REGULATION OF PLATELET ACTIVATION | 29 | -0.15 | -0.47 | 0.981 | 1.000 | 1.000 | 30306 | tags=48%, list=55%, signal=108% | |
5559 | REGULATION OF PHAGOCYTOSIS, ENGULFMENT | 12 | -0.19 | -0.47 | 0.989 | 1.000 | 1.000 | 28163 | tags=42%, list=52%, signal=86% | |
5560 | B CELL RECEPTOR SIGNALING PATHWAY | 56 | -0.14 | -0.46 | 0.982 | 1.000 | 1.000 | 17631 | tags=27%, list=32%, signal=39% | |
5561 | REGULATION OF SARCOMERE ORGANIZATION | 13 | -0.19 | -0.46 | 0.972 | 1.000 | 1.000 | 42517 | tags=92%, list=78%, signal=415% | |
5562 | POSITIVE REGULATION OF CALCIUM ION TRANSPORT INTO CYTOSOL | 80 | -0.12 | -0.46 | 1.000 | 1.000 | 1.000 | 20627 | tags=31%, list=38%, signal=50% | |
5563 | REGULATION OF SYNAPSE ASSEMBLY | 63 | -0.13 | -0.46 | 0.981 | 1.000 | 1.000 | 37805 | tags=62%, list=69%, signal=200% | |
5564 | REGULATION OF BONE RESORPTION | 43 | -0.14 | -0.46 | 0.983 | 1.000 | 1.000 | 39506 | tags=67%, list=72%, signal=243% | |
5565 | POSITIVE REGULATION OF TUMOR NECROSIS FACTOR BIOSYNTHETIC PROCESS | 22 | -0.17 | -0.46 | 0.970 | 1.000 | 1.000 | 40173 | tags=77%, list=73%, signal=291% | |
5566 | POSITIVE REGULATION OF T CELL MIGRATION | 33 | -0.16 | -0.46 | 0.974 | 1.000 | 1.000 | 41802 | tags=79%, list=76%, signal=334% | |
5567 | REGULATION OF WOUND HEALING | 221 | -0.12 | -0.46 | 0.994 | 1.000 | 1.000 | 41033 | tags=71%, list=75%, signal=282% | |
5568 | COLLAGEN CATABOLIC PROCESS | 153 | -0.12 | -0.46 | 0.991 | 1.000 | 1.000 | 37791 | tags=58%, list=69%, signal=188% | |
5569 | REGULATION OF INTERFERON-GAMMA SECRETION | 14 | -0.19 | -0.46 | 0.988 | 1.000 | 1.000 | 36178 | tags=64%, list=66%, signal=190% | |
5570 | POSITIVE REGULATION OF MYOTUBE DIFFERENTIATION | 44 | -0.16 | -0.46 | 0.986 | 1.000 | 1.000 | 13224 | tags=20%, list=24%, signal=27% | |
5571 | LYMPHOCYTE MEDIATED IMMUNITY | 180 | -0.12 | -0.46 | 0.982 | 1.000 | 1.000 | 24731 | tags=36%, list=45%, signal=65% | |
5572 | ACUTE INFLAMMATORY RESPONSE | 50 | -0.15 | -0.46 | 0.984 | 1.000 | 1.000 | 9213 | tags=16%, list=17%, signal=19% | |
5573 | MULTICELLULAR ORGANISMAL CATABOLIC PROCESS | 155 | -0.12 | -0.46 | 0.987 | 1.000 | 1.000 | 37791 | tags=58%, list=69%, signal=187% | |
5574 | RENAL VESICLE MORPHOGENESIS | 17 | -0.17 | -0.46 | 0.969 | 1.000 | 1.000 | 32287 | tags=53%, list=59%, signal=129% | |
5575 | REGULATION OF CALCIUM ION TRANSPORT INTO CYTOSOL | 167 | -0.11 | -0.46 | 1.000 | 1.000 | 1.000 | 23015 | tags=34%, list=42%, signal=59% | |
5576 | RENAL FILTRATION | 45 | -0.14 | -0.46 | 0.990 | 1.000 | 1.000 | 13245 | tags=20%, list=24%, signal=26% | |
5577 | REGULATION OF DOPAMINE UPTAKE INVOLVED IN SYNAPTIC TRANSMISSION | 19 | -0.17 | -0.46 | 0.964 | 1.000 | 1.000 | 41997 | tags=84%, list=77%, signal=363% | |
5578 | REGULATION OF CATECHOLAMINE UPTAKE INVOLVED IN SYNAPTIC TRANSMISSION | 19 | -0.17 | -0.46 | 0.964 | 1.000 | 1.000 | 41997 | tags=84%, list=77%, signal=363% | |
5579 | APPENDAGE MORPHOGENESIS | 115 | -0.11 | -0.46 | 0.991 | 1.000 | 1.000 | 24557 | tags=35%, list=45%, signal=63% | |
5580 | LIMB MORPHOGENESIS | 115 | -0.11 | -0.46 | 0.991 | 1.000 | 1.000 | 24557 | tags=35%, list=45%, signal=63% | |
5581 | NEGATIVE REGULATION OF PURINE NUCLEOTIDE METABOLIC PROCESS | 71 | -0.13 | -0.46 | 0.992 | 1.000 | 1.000 | 21623 | tags=30%, list=40%, signal=49% | |
5582 | REGULATION OF CYCLIC NUCLEOTIDE METABOLIC PROCESS | 223 | -0.11 | -0.46 | 0.994 | 1.000 | 1.000 | 30255 | tags=43%, list=55%, signal=96% | |
5583 | RESPONSE TO ISOQUINOLINE ALKALOID | 13 | -0.19 | -0.46 | 0.981 | 1.000 | 1.000 | 16185 | tags=23%, list=30%, signal=33% | |
5584 | RESPONSE TO MORPHINE | 13 | -0.19 | -0.46 | 0.981 | 1.000 | 1.000 | 16185 | tags=23%, list=30%, signal=33% | |
5585 | NEGATIVE REGULATION OF LEUKOCYTE CHEMOTAXIS | 19 | -0.16 | -0.46 | 0.989 | 1.000 | 1.000 | 16930 | tags=26%, list=31%, signal=38% | |
5586 | NEGATIVE REGULATION OF CHEMOTAXIS | 57 | -0.13 | -0.45 | 0.985 | 1.000 | 1.000 | 43697 | tags=84%, list=80%, signal=419% | |
5587 | RESPONSE TO CAFFEINE | 18 | -0.15 | -0.45 | 0.989 | 1.000 | 1.000 | 17609 | tags=22%, list=32%, signal=33% | |
5588 | CELLULAR RESPONSE TO CAFFEINE | 18 | -0.15 | -0.45 | 0.989 | 1.000 | 1.000 | 17609 | tags=22%, list=32%, signal=33% | |
5589 | CELLULAR RESPONSE TO PURINE-CONTAINING COMPOUND | 18 | -0.15 | -0.45 | 0.989 | 1.000 | 1.000 | 17609 | tags=22%, list=32%, signal=33% | |
5590 | CARDIAC MUSCLE CELL CONTRACTION | 42 | -0.12 | -0.45 | 0.990 | 1.000 | 1.000 | 26088 | tags=38%, list=48%, signal=73% | |
5591 | RESPONSE TO X-RAY | 22 | -0.18 | -0.45 | 0.973 | 1.000 | 1.000 | 41619 | tags=86%, list=76%, signal=362% | |
5592 | T-HELPER 17 TYPE IMMUNE RESPONSE | 21 | -0.17 | -0.45 | 0.977 | 1.000 | 1.000 | 37233 | tags=67%, list=68%, signal=209% | |
5593 | T-HELPER 17 CELL DIFFERENTIATION | 21 | -0.17 | -0.45 | 0.977 | 1.000 | 1.000 | 37233 | tags=67%, list=68%, signal=209% | |
5594 | REGULATION OF ION HOMEOSTASIS | 313 | -0.10 | -0.45 | 1.000 | 1.000 | 1.000 | 39090 | tags=64%, list=71%, signal=223% | |
5595 | NEGATIVE REGULATION OF NUCLEOTIDE METABOLIC PROCESS | 72 | -0.12 | -0.45 | 0.996 | 1.000 | 1.000 | 21623 | tags=29%, list=40%, signal=48% | |
5596 | CARDIAC CELL DEVELOPMENT | 89 | -0.11 | -0.45 | 0.996 | 1.000 | 1.000 | 37799 | tags=63%, list=69%, signal=204% | |
5597 | POSITIVE REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 37 | -0.13 | -0.45 | 0.982 | 1.000 | 1.000 | 28154 | tags=41%, list=51%, signal=84% | |
5598 | BLOOD CIRCULATION | 443 | -0.10 | -0.45 | 1.000 | 1.000 | 1.000 | 34564 | tags=52%, list=63%, signal=141% | |
5599 | LEUKOCYTE TETHERING OR ROLLING | 23 | -0.14 | -0.45 | 0.992 | 1.000 | 1.000 | 42715 | tags=91%, list=78%, signal=417% | |
5600 | NEGATIVE REGULATION OF FIBRINOLYSIS | 21 | -0.16 | -0.45 | 0.981 | 1.000 | 1.000 | 5047 | tags=14%, list=9%, signal=16% | |
5601 | NEPHRON TUBULE MORPHOGENESIS | 61 | -0.12 | -0.45 | 0.984 | 1.000 | 1.000 | 17093 | tags=23%, list=31%, signal=33% | |
5602 | NEGATIVE REGULATION OF ADENYLATE CYCLASE ACTIVITY | 36 | -0.14 | -0.45 | 0.988 | 1.000 | 1.000 | 29862 | tags=42%, list=55%, signal=92% | |
5603 | POSITIVE REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 30 | -0.15 | -0.45 | 0.992 | 1.000 | 1.000 | 29931 | tags=47%, list=55%, signal=103% | |
5604 | NEGATIVE REGULATION OF NUCLEOTIDE BIOSYNTHETIC PROCESS | 53 | -0.13 | -0.45 | 0.994 | 1.000 | 1.000 | 20627 | tags=28%, list=38%, signal=45% | |
5605 | NEGATIVE REGULATION OF PURINE NUCLEOTIDE BIOSYNTHETIC PROCESS | 53 | -0.13 | -0.45 | 0.994 | 1.000 | 1.000 | 20627 | tags=28%, list=38%, signal=45% | |
5606 | NEGATIVE REGULATION OF BEHAVIOR | 59 | -0.13 | -0.44 | 0.990 | 1.000 | 1.000 | 43697 | tags=83%, list=80%, signal=413% | |
5607 | MULTICELLULAR ORGANISMAL MACROMOLECULE METABOLIC PROCESS | 168 | -0.11 | -0.44 | 0.990 | 1.000 | 1.000 | 37791 | tags=58%, list=69%, signal=186% | |
5608 | CIRCULATORY SYSTEM PROCESS | 444 | -0.10 | -0.44 | 1.000 | 1.000 | 1.000 | 34564 | tags=52%, list=63%, signal=140% | |
5609 | NEPHRON TUBULE DEVELOPMENT | 78 | -0.12 | -0.44 | 0.996 | 1.000 | 1.000 | 33971 | tags=50%, list=62%, signal=132% | |
5610 | METANEPHROS DEVELOPMENT | 92 | -0.12 | -0.44 | 0.987 | 1.000 | 1.000 | 33291 | tags=51%, list=61%, signal=130% | |
5611 | SYNAPSE ASSEMBLY | 113 | -0.11 | -0.44 | 0.998 | 1.000 | 1.000 | 35103 | tags=57%, list=64%, signal=158% | |
5612 | MYOTUBE CELL DEVELOPMENT | 13 | -0.17 | -0.44 | 0.984 | 1.000 | 1.000 | 6207 | tags=15%, list=11%, signal=17% | |
5613 | POSITIVE REGULATION OF AMINE TRANSPORT | 24 | -0.14 | -0.44 | 0.998 | 1.000 | 1.000 | 37082 | tags=75%, list=68%, signal=233% | |
5614 | DEFENSE RESPONSE TO GRAM-NEGATIVE BACTERIUM | 84 | -0.13 | -0.44 | 0.979 | 1.000 | 1.000 | 17837 | tags=24%, list=33%, signal=35% | |
5615 | MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 176 | -0.11 | -0.44 | 0.994 | 1.000 | 1.000 | 37791 | tags=57%, list=69%, signal=185% | |
5616 | POSITIVE REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR PRODUCTION | 68 | -0.14 | -0.44 | 0.987 | 1.000 | 1.000 | 37806 | tags=62%, list=69%, signal=200% | |
5617 | EMBRYONIC LIMB MORPHOGENESIS | 80 | -0.11 | -0.44 | 0.989 | 1.000 | 1.000 | 18930 | tags=25%, list=35%, signal=38% | |
5618 | EMBRYONIC APPENDAGE MORPHOGENESIS | 80 | -0.11 | -0.44 | 0.989 | 1.000 | 1.000 | 18930 | tags=25%, list=35%, signal=38% | |
5619 | LEUKOCYTE CHEMOTAXIS | 130 | -0.13 | -0.44 | 0.988 | 1.000 | 1.000 | 22408 | tags=32%, list=41%, signal=55% | |
5620 | VERY-LOW-DENSITY LIPOPROTEIN PARTICLE REMODELING | 14 | -0.18 | -0.44 | 0.988 | 1.000 | 1.000 | 12819 | tags=21%, list=23%, signal=28% | |
5621 | REGULATION OF CYCLIC NUCLEOTIDE BIOSYNTHETIC PROCESS | 182 | -0.11 | -0.44 | 0.996 | 1.000 | 1.000 | 30167 | tags=42%, list=55%, signal=93% | |
5622 | COLLAGEN METABOLIC PROCESS | 167 | -0.11 | -0.44 | 0.994 | 1.000 | 1.000 | 37791 | tags=57%, list=69%, signal=186% | |
5623 | REGULATION OF CELL CHEMOTAXIS TO FIBROBLAST GROWTH FACTOR | 22 | -0.17 | -0.44 | 0.966 | 1.000 | 1.000 | 12424 | tags=18%, list=23%, signal=24% | |
5624 | REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS TO FIBROBLAST GROWTH FACTOR | 22 | -0.17 | -0.44 | 0.966 | 1.000 | 1.000 | 12424 | tags=18%, list=23%, signal=24% | |
5625 | MEMBRANE DEPOLARIZATION DURING ACTION POTENTIAL | 35 | -0.13 | -0.44 | 0.994 | 1.000 | 1.000 | 25209 | tags=37%, list=46%, signal=69% | |
5626 | NEGATIVE REGULATION OF INTERLEUKIN-12 PRODUCTION | 28 | -0.14 | -0.43 | 0.978 | 1.000 | 1.000 | 34905 | tags=61%, list=64%, signal=168% | |
5627 | POSITIVE REGULATION OF INTERLEUKIN-8 BIOSYNTHETIC PROCESS | 16 | -0.19 | -0.43 | 0.992 | 1.000 | 1.000 | 4626 | tags=13%, list=8%, signal=14% | |
5628 | CARDIAC MUSCLE CELL ACTION POTENTIAL INVOLVED IN CONTRACTION | 37 | -0.12 | -0.43 | 0.992 | 1.000 | 1.000 | 25209 | tags=35%, list=46%, signal=65% | |
5629 | REGULATION OF OSTEOCLAST DIFFERENTIATION | 52 | -0.14 | -0.43 | 0.988 | 1.000 | 1.000 | 25520 | tags=37%, list=47%, signal=68% | |
5630 | REGULATION OF CELL MIGRATION INVOLVED IN SPROUTING ANGIOGENESIS | 42 | -0.13 | -0.43 | 0.994 | 1.000 | 1.000 | 37015 | tags=62%, list=68%, signal=192% | |
5631 | POSITIVE REGULATION OF LYMPHOCYTE MIGRATION | 38 | -0.14 | -0.43 | 0.988 | 1.000 | 1.000 | 41802 | tags=76%, list=76%, signal=324% | |
5632 | REGULATION OF CALCIUM ION IMPORT | 178 | -0.10 | -0.43 | 1.000 | 1.000 | 1.000 | 23015 | tags=34%, list=42%, signal=58% | |
5633 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION OF BITTER TASTE | 31 | -0.14 | -0.43 | 0.979 | 1.000 | 1.000 | 43323 | tags=77%, list=79%, signal=373% | |
5634 | DETECTION OF CHEMICAL STIMULUS | 122 | -0.11 | -0.43 | 0.996 | 1.000 | 1.000 | 42796 | tags=69%, list=78%, signal=316% | |
5635 | POSITIVE REGULATION OF SYNAPSE ASSEMBLY | 38 | -0.13 | -0.43 | 0.986 | 1.000 | 1.000 | 16486 | tags=24%, list=30%, signal=34% | |
5636 | FIBRINOLYSIS | 28 | -0.16 | -0.42 | 0.974 | 1.000 | 1.000 | 40547 | tags=71%, list=74%, signal=276% | |
5637 | REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE BY HORMONE | 44 | -0.13 | -0.42 | 0.994 | 1.000 | 1.000 | 13274 | tags=18%, list=24%, signal=24% | |
5638 | SA NODE CELL ACTION POTENTIAL | 14 | -0.15 | -0.42 | 0.996 | 1.000 | 1.000 | 25209 | tags=36%, list=46%, signal=66% | |
5639 | SA NODE CELL TO ATRIAL CARDIAC MUSCLE CELL SIGNALLING | 14 | -0.15 | -0.42 | 0.996 | 1.000 | 1.000 | 25209 | tags=36%, list=46%, signal=66% | |
5640 | SA NODE CELL TO ATRIAL CARDIAC MUSCLE CELL COMMUNICATION | 14 | -0.15 | -0.42 | 0.996 | 1.000 | 1.000 | 25209 | tags=36%, list=46%, signal=66% | |
5641 | NEGATIVE REGULATION OF CAMP METABOLIC PROCESS | 48 | -0.12 | -0.42 | 0.994 | 1.000 | 1.000 | 20627 | tags=27%, list=38%, signal=43% | |
5642 | SUPEROXIDE ANION GENERATION | 17 | -0.16 | -0.42 | 0.992 | 1.000 | 1.000 | 32513 | tags=59%, list=59%, signal=145% | |
5643 | RETINA VASCULATURE MORPHOGENESIS IN CAMERA-TYPE EYE | 14 | -0.17 | -0.42 | 0.990 | 1.000 | 1.000 | 36746 | tags=64%, list=67%, signal=196% | |
5644 | PROTEIN KINASE A SIGNALING | 14 | -0.16 | -0.42 | 0.991 | 1.000 | 1.000 | 34794 | tags=57%, list=64%, signal=157% | |
5645 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 53 | -0.13 | -0.42 | 0.990 | 1.000 | 1.000 | 42715 | tags=83%, list=78%, signal=379% | |
5646 | COMPLEMENT RECEPTOR MEDIATED SIGNALING PATHWAY | 14 | -0.19 | -0.42 | 0.988 | 1.000 | 1.000 | 32204 | tags=64%, list=59%, signal=156% | |
5647 | POSITIVE REGULATION OF STEROID BIOSYNTHETIC PROCESS | 19 | -0.16 | -0.42 | 0.990 | 1.000 | 1.000 | 229 | tags=5%, list=0%, signal=5% | |
5648 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION OF TASTE | 36 | -0.13 | -0.42 | 0.983 | 1.000 | 1.000 | 37888 | tags=61%, list=69%, signal=199% | |
5649 | L-AMINO ACID IMPORT | 16 | -0.16 | -0.42 | 0.982 | 1.000 | 1.000 | 33992 | tags=63%, list=62%, signal=165% | |
5650 | MAINTENANCE OF CELL POLARITY | 22 | -0.13 | -0.42 | 0.996 | 1.000 | 1.000 | 4925 | tags=9%, list=9%, signal=10% | |
5651 | POSITIVE REGULATION OF OSTEOBLAST DIFFERENTIATION | 85 | -0.12 | -0.42 | 0.998 | 1.000 | 1.000 | 40414 | tags=66%, list=74%, signal=252% | |
5652 | ENDOCRINE SYSTEM DEVELOPMENT | 150 | -0.10 | -0.42 | 1.000 | 1.000 | 1.000 | 23316 | tags=32%, list=43%, signal=56% | |
5653 | POSITIVE REGULATION OF VASOCONSTRICTION | 15 | -0.17 | -0.42 | 0.992 | 1.000 | 1.000 | 1266 | tags=7%, list=2%, signal=7% | |
5654 | CARDIAC MUSCLE CELL PROLIFERATION | 12 | -0.15 | -0.41 | 0.996 | 1.000 | 1.000 | 21991 | tags=33%, list=40%, signal=56% | |
5655 | POSITIVE REGULATION OF BLOOD COAGULATION | 39 | -0.14 | -0.41 | 0.988 | 1.000 | 1.000 | 5047 | tags=13%, list=9%, signal=14% | |
5656 | POSITIVE REGULATION OF COAGULATION | 39 | -0.14 | -0.41 | 0.988 | 1.000 | 1.000 | 5047 | tags=13%, list=9%, signal=14% | |
5657 | POSITIVE REGULATION OF HEMOSTASIS | 39 | -0.14 | -0.41 | 0.988 | 1.000 | 1.000 | 5047 | tags=13%, list=9%, signal=14% | |
5658 | POSITIVE REGULATION OF INTERLEUKIN-2 BIOSYNTHETIC PROCESS | 11 | -0.20 | -0.41 | 0.994 | 1.000 | 1.000 | 14287 | tags=27%, list=26%, signal=37% | |
5659 | NEGATIVE REGULATION OF CAMP BIOSYNTHETIC PROCESS | 44 | -0.12 | -0.41 | 0.996 | 1.000 | 1.000 | 20627 | tags=27%, list=38%, signal=44% | |
5660 | NEGATIVE REGULATION OF WOUND HEALING | 96 | -0.12 | -0.41 | 0.988 | 1.000 | 1.000 | 41033 | tags=70%, list=75%, signal=279% | |
5661 | GENITALIA DEVELOPMENT | 42 | -0.11 | -0.41 | 0.991 | 1.000 | 1.000 | 33218 | tags=50%, list=61%, signal=127% | |
5662 | REGULATION OF ORGAN FORMATION | 20 | -0.13 | -0.41 | 1.000 | 1.000 | 1.000 | 4503 | tags=10%, list=8%, signal=11% | |
5663 | REGULATION OF POTASSIUM ION TRANSPORT | 139 | -0.09 | -0.41 | 1.000 | 1.000 | 1.000 | 15979 | tags=22%, list=29%, signal=31% | |
5664 | RESPONSE TO PROTOZOAN | 15 | -0.16 | -0.41 | 0.994 | 1.000 | 1.000 | 37727 | tags=80%, list=69%, signal=258% | |
5665 | DEFENSE RESPONSE TO PROTOZOAN | 15 | -0.16 | -0.41 | 0.994 | 1.000 | 1.000 | 37727 | tags=80%, list=69%, signal=258% | |
5666 | PEPTIDYL-L-CYSTEINE S-PALMITOYLATION | 16 | -0.14 | -0.41 | 0.998 | 1.000 | 1.000 | 22407 | tags=38%, list=41%, signal=64% | |
5667 | PEPTIDYL-S-DIACYLGLYCEROL-L-CYSTEINE BIOSYNTHETIC PROCESS FROM PEPTIDYL-CYSTEINE | 16 | -0.14 | -0.41 | 0.998 | 1.000 | 1.000 | 22407 | tags=38%, list=41%, signal=64% | |
5668 | NEGATIVE REGULATION OF LEUKOCYTE MIGRATION | 43 | -0.12 | -0.40 | 1.000 | 1.000 | 1.000 | 43697 | tags=77%, list=80%, signal=382% | |
5669 | REGULATION OF LYMPHOCYTE CHEMOTAXIS | 31 | -0.14 | -0.40 | 0.998 | 1.000 | 1.000 | 41851 | tags=77%, list=77%, signal=330% | |
5670 | POSITIVE REGULATION OF RELEASE OF SEQUESTERED CALCIUM ION INTO CYTOSOL | 73 | -0.11 | -0.40 | 0.998 | 1.000 | 1.000 | 20627 | tags=30%, list=38%, signal=48% | |
5671 | RENAL TUBULE DEVELOPMENT | 82 | -0.11 | -0.40 | 0.992 | 1.000 | 1.000 | 35541 | tags=52%, list=65%, signal=150% | |
5672 | POSITIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA PRODUCTION | 21 | -0.14 | -0.40 | 0.998 | 1.000 | 1.000 | 8136 | tags=14%, list=15%, signal=17% | |
5673 | REGULATION OF GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR PRODUCTION | 21 | -0.14 | -0.40 | 0.994 | 1.000 | 1.000 | 32149 | tags=52%, list=59%, signal=127% | |
5674 | NEGATIVE REGULATION OF B CELL PROLIFERATION | 24 | -0.14 | -0.40 | 0.994 | 1.000 | 1.000 | 17156 | tags=25%, list=31%, signal=36% | |
5675 | CYCLIC NUCLEOTIDE CATABOLIC PROCESS | 33 | -0.13 | -0.40 | 0.996 | 1.000 | 1.000 | 1615 | tags=6%, list=3%, signal=6% | |
5676 | TRIGLYCERIDE-RICH LIPOPROTEIN PARTICLE REMODELING | 16 | -0.16 | -0.40 | 0.992 | 1.000 | 1.000 | 12819 | tags=19%, list=23%, signal=24% | |
5677 | REGULATION OF SMOOTH MUSCLE CELL MIGRATION | 76 | -0.11 | -0.40 | 0.994 | 1.000 | 1.000 | 41904 | tags=72%, list=77%, signal=309% | |
5678 | NEGATIVE REGULATION OF INTERLEUKIN-1 PRODUCTION | 18 | -0.16 | -0.40 | 0.988 | 1.000 | 1.000 | 30177 | tags=44%, list=55%, signal=99% | |
5679 | RENAL VESICLE DEVELOPMENT | 18 | -0.15 | -0.40 | 0.994 | 1.000 | 1.000 | 32287 | tags=50%, list=59%, signal=122% | |
5680 | POSITIVE REGULATION OF ACTIN CYTOSKELETON REORGANIZATION | 25 | -0.13 | -0.40 | 0.996 | 1.000 | 1.000 | 19450 | tags=24%, list=36%, signal=37% | |
5681 | REGULATION OF METANEPHROS DEVELOPMENT | 33 | -0.13 | -0.40 | 0.982 | 1.000 | 1.000 | 40903 | tags=76%, list=75%, signal=301% | |
5682 | NEGATIVE REGULATION OF CYTOKINE-MEDIATED SIGNALING PATHWAY | 70 | -0.12 | -0.40 | 0.996 | 1.000 | 1.000 | 47366 | tags=90%, list=87%, signal=672% | |
5683 | NEGATIVE REGULATION OF INTERLEUKIN-1 SECRETION | 10 | -0.19 | -0.39 | 0.996 | 1.000 | 1.000 | 30177 | tags=50%, list=55%, signal=112% | |
5684 | SYNAPTIC TRANSMISSION | 927 | -0.09 | -0.39 | 1.000 | 1.000 | 1.000 | 37177 | tags=57%, list=68%, signal=174% | |
5685 | SYNAPTIC SIGNALING | 927 | -0.09 | -0.39 | 1.000 | 1.000 | 1.000 | 37177 | tags=57%, list=68%, signal=174% | |
5686 | TRANS-SYNAPTIC SIGNALING | 927 | -0.09 | -0.39 | 1.000 | 1.000 | 1.000 | 37177 | tags=57%, list=68%, signal=174% | |
5687 | POSITIVE REGULATION OF INOSITOL PHOSPHATE BIOSYNTHETIC PROCESS | 11 | -0.16 | -0.39 | 1.000 | 1.000 | 1.000 | 41997 | tags=82%, list=77%, signal=353% | |
5688 | LIPID STORAGE | 26 | -0.15 | -0.39 | 0.994 | 1.000 | 1.000 | 46581 | tags=100%, list=85%, signal=675% | |
5689 | POSITIVE REGULATION OF METANEPHROS DEVELOPMENT | 30 | -0.14 | -0.39 | 0.992 | 1.000 | 1.000 | 40903 | tags=77%, list=75%, signal=304% | |
5690 | T CELL PROLIFERATION | 23 | -0.15 | -0.39 | 0.986 | 1.000 | 1.000 | 31207 | tags=57%, list=57%, signal=132% | |
5691 | LEARNING OR MEMORY | 166 | -0.09 | -0.39 | 1.000 | 1.000 | 1.000 | 42572 | tags=72%, list=78%, signal=326% | |
5692 | REGULATION OF DOPAMINE SECRETION | 23 | -0.14 | -0.39 | 0.998 | 1.000 | 1.000 | 14129 | tags=22%, list=26%, signal=29% | |
5693 | PHOSPHATE ION HOMEOSTASIS | 23 | -0.13 | -0.39 | 0.998 | 1.000 | 1.000 | 24557 | tags=39%, list=45%, signal=71% | |
5694 | TRIVALENT INORGANIC ANION HOMEOSTASIS | 23 | -0.13 | -0.39 | 0.998 | 1.000 | 1.000 | 24557 | tags=39%, list=45%, signal=71% | |
5695 | REGULATION OF RELEASE OF SEQUESTERED CALCIUM ION INTO CYTOSOL | 144 | -0.09 | -0.39 | 1.000 | 1.000 | 1.000 | 23015 | tags=33%, list=42%, signal=57% | |
5696 | POSITIVE REGULATION OF BLOOD CIRCULATION | 78 | -0.10 | -0.39 | 0.994 | 1.000 | 1.000 | 13376 | tags=17%, list=24%, signal=22% | |
5697 | POSITIVE REGULATION OF PODOSOME ASSEMBLY | 7 | -0.21 | -0.38 | 0.994 | 1.000 | 1.000 | 33536 | tags=57%, list=61%, signal=148% | |
5698 | ICOSANOID SECRETION | 21 | -0.12 | -0.38 | 1.000 | 1.000 | 1.000 | 226 | tags=5%, list=0%, signal=5% | |
5699 | ICOSANOID TRANSPORT | 21 | -0.12 | -0.38 | 1.000 | 1.000 | 1.000 | 226 | tags=5%, list=0%, signal=5% | |
5700 | FATTY ACID DERIVATIVE TRANSPORT | 21 | -0.12 | -0.38 | 1.000 | 1.000 | 1.000 | 226 | tags=5%, list=0%, signal=5% | |
5701 | REGULATION OF B CELL PROLIFERATION | 87 | -0.11 | -0.38 | 0.994 | 1.000 | 1.000 | 30386 | tags=43%, list=56%, signal=96% | |
5702 | POSITIVE REGULATION OF STRIATED MUSCLE CELL DIFFERENTIATION | 79 | -0.12 | -0.38 | 0.992 | 1.000 | 1.000 | 35905 | tags=56%, list=66%, signal=162% | |
5703 | NEGATIVE REGULATION OF BLOOD CIRCULATION | 55 | -0.10 | -0.38 | 1.000 | 1.000 | 1.000 | 33809 | tags=51%, list=62%, signal=133% | |
5704 | EMBRYONIC FORELIMB MORPHOGENESIS | 24 | -0.12 | -0.38 | 1.000 | 1.000 | 1.000 | 45286 | tags=88%, list=83%, signal=509% | |
5705 | B CELL PROLIFERATION | 23 | -0.14 | -0.38 | 0.998 | 1.000 | 1.000 | 38947 | tags=65%, list=71%, signal=227% | |
5706 | REGULATION OF INTERLEUKIN-8 BIOSYNTHETIC PROCESS | 27 | -0.14 | -0.38 | 1.000 | 1.000 | 1.000 | 43739 | tags=81%, list=80%, signal=407% | |
5707 | SUBSTRATE-DEPENDENT CELL MIGRATION | 28 | -0.12 | -0.38 | 1.000 | 1.000 | 1.000 | 17311 | tags=25%, list=32%, signal=37% | |
5708 | NEGATIVE REGULATION OF VASCULAR PERMEABILITY | 16 | -0.14 | -0.38 | 1.000 | 1.000 | 1.000 | 12097 | tags=19%, list=22%, signal=24% | |
5709 | RENAL TUBULE MORPHOGENESIS | 70 | -0.10 | -0.37 | 0.996 | 1.000 | 1.000 | 33971 | tags=49%, list=62%, signal=128% | |
5710 | GLOMERULAR FILTRATION | 44 | -0.11 | -0.37 | 0.996 | 1.000 | 1.000 | 13245 | tags=18%, list=24%, signal=24% | |
5711 | MONONUCLEAR CELL PROLIFERATION | 51 | -0.13 | -0.37 | 0.996 | 1.000 | 1.000 | 30091 | tags=49%, list=55%, signal=109% | |
5712 | LYMPHOCYTE PROLIFERATION | 51 | -0.13 | -0.37 | 0.996 | 1.000 | 1.000 | 30091 | tags=49%, list=55%, signal=109% | |
5713 | VISUAL LEARNING | 35 | -0.11 | -0.37 | 0.998 | 1.000 | 1.000 | 1704 | tags=6%, list=3%, signal=6% | |
5714 | REGULATION OF COAGULATION | 143 | -0.10 | -0.37 | 0.996 | 1.000 | 1.000 | 25719 | tags=37%, list=47%, signal=70% | |
5715 | REGULATION OF B CELL RECEPTOR SIGNALING PATHWAY | 22 | -0.14 | -0.37 | 0.994 | 1.000 | 1.000 | 13664 | tags=23%, list=25%, signal=30% | |
5716 | REGULATION OF BLOOD COAGULATION | 141 | -0.10 | -0.37 | 0.998 | 1.000 | 1.000 | 25719 | tags=37%, list=47%, signal=69% | |
5717 | REGULATION OF HEMOSTASIS | 141 | -0.10 | -0.37 | 0.998 | 1.000 | 1.000 | 25719 | tags=37%, list=47%, signal=69% | |
5718 | HUMORAL IMMUNE RESPONSE | 246 | -0.10 | -0.37 | 0.990 | 1.000 | 1.000 | 28294 | tags=39%, list=52%, signal=81% | |
5719 | DIVALENT INORGANIC ANION HOMEOSTASIS | 24 | -0.12 | -0.36 | 0.998 | 1.000 | 1.000 | 24557 | tags=38%, list=45%, signal=68% | |
5720 | LIPOPOLYSACCHARIDE-MEDIATED SIGNALING PATHWAY | 50 | -0.13 | -0.36 | 0.996 | 1.000 | 1.000 | 40469 | tags=68%, list=74%, signal=261% | |
5721 | PHOSPHOLIPASE C-ACTIVATING G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 82 | -0.10 | -0.36 | 0.998 | 1.000 | 1.000 | 36736 | tags=54%, list=67%, signal=163% | |
5722 | ANTIBACTERIAL HUMORAL RESPONSE | 98 | -0.10 | -0.36 | 0.996 | 1.000 | 1.000 | 14697 | tags=18%, list=27%, signal=25% | |
5723 | REGULATION OF ENDOCYTIC RECYCLING | 20 | -0.16 | -0.36 | 0.996 | 1.000 | 1.000 | 36398 | tags=70%, list=67%, signal=209% | |
5724 | REGULATION OF SKELETAL MUSCLE CELL DIFFERENTIATION | 26 | -0.12 | -0.36 | 0.998 | 1.000 | 1.000 | 29526 | tags=42%, list=54%, signal=92% | |
5725 | PHOSPHOLIPID HOMEOSTASIS | 22 | -0.12 | -0.35 | 0.998 | 1.000 | 1.000 | 16531 | tags=23%, list=30%, signal=33% | |
5726 | POSITIVE REGULATION OF CALCIUM ION IMPORT | 89 | -0.09 | -0.35 | 1.000 | 1.000 | 1.000 | 22928 | tags=33%, list=42%, signal=56% | |
5727 | NEGATIVE REGULATION OF INTERLEUKIN-1 BETA PRODUCTION | 13 | -0.15 | -0.35 | 0.998 | 1.000 | 1.000 | 30177 | tags=38%, list=55%, signal=86% | |
5728 | POSITIVE REGULATION OF GLOMERULUS DEVELOPMENT | 14 | -0.14 | -0.35 | 0.996 | 1.000 | 1.000 | 6145 | tags=14%, list=11%, signal=16% | |
5729 | REGULATION OF PLASMINOGEN ACTIVATION | 21 | -0.12 | -0.35 | 0.998 | 1.000 | 1.000 | 36972 | tags=67%, list=68%, signal=206% | |
5730 | METANEPHRIC NEPHRON DEVELOPMENT | 40 | -0.11 | -0.34 | 0.990 | 1.000 | 1.000 | 32287 | tags=48%, list=59%, signal=116% | |
5731 | CELL VOLUME HOMEOSTASIS | 23 | -0.10 | -0.34 | 1.000 | 1.000 | 1.000 | 21231 | tags=30%, list=39%, signal=50% | |
5732 | CGMP METABOLIC PROCESS | 30 | -0.10 | -0.33 | 0.998 | 1.000 | 1.000 | 29333 | tags=40%, list=54%, signal=86% | |
5733 | HEXOSE TRANSMEMBRANE TRANSPORT | 17 | -0.14 | -0.33 | 1.000 | 1.000 | 1.000 | 22253 | tags=35%, list=41%, signal=59% | |
5734 | GLUCOSE TRANSMEMBRANE TRANSPORT | 17 | -0.14 | -0.33 | 1.000 | 1.000 | 1.000 | 22253 | tags=35%, list=41%, signal=59% | |
5735 | LEARNING | 96 | -0.08 | -0.33 | 1.000 | 1.000 | 1.000 | 2190 | tags=5%, list=4%, signal=5% | |
5736 | REGULATION OF ENDOTHELIAL CELL DEVELOPMENT | 20 | -0.12 | -0.33 | 1.000 | 1.000 | 1.000 | 13491 | tags=20%, list=25%, signal=27% | |
5737 | REGULATION OF ESTABLISHMENT OF ENDOTHELIAL BARRIER | 20 | -0.12 | -0.33 | 1.000 | 1.000 | 1.000 | 13491 | tags=20%, list=25%, signal=27% | |
5738 | URETERIC BUD MORPHOGENESIS | 44 | -0.10 | -0.33 | 0.996 | 1.000 | 1.000 | 33291 | tags=45%, list=61%, signal=116% | |
5739 | ANTIMICROBIAL HUMORAL RESPONSE | 101 | -0.09 | -0.33 | 0.998 | 1.000 | 1.000 | 10050 | tags=13%, list=18%, signal=16% | |
5740 | REGULATION OF GLOMERULUS DEVELOPMENT | 21 | -0.12 | -0.32 | 1.000 | 1.000 | 1.000 | 40903 | tags=76%, list=75%, signal=302% | |
5741 | REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE MEDIATED BY A CHEMICAL SIGNAL | 59 | -0.10 | -0.32 | 1.000 | 1.000 | 1.000 | 38311 | tags=59%, list=70%, signal=198% | |
5742 | REGULATION OF N-METHYL-D-ASPARTATE SELECTIVE GLUTAMATE RECEPTOR ACTIVITY | 27 | -0.10 | -0.32 | 1.000 | 1.000 | 1.000 | 7877 | tags=11%, list=14%, signal=13% | |
5743 | ENDOCRINE PROCESS | 68 | -0.09 | -0.31 | 0.996 | 1.000 | 1.000 | 13274 | tags=16%, list=24%, signal=21% | |
5744 | VASCULAR PROCESS IN CIRCULATORY SYSTEM | 159 | -0.08 | -0.31 | 1.000 | 1.000 | 1.000 | 39258 | tags=58%, list=72%, signal=207% | |
5745 | REGULATION OF CELL PROLIFERATION INVOLVED IN KIDNEY DEVELOPMENT | 22 | -0.11 | -0.31 | 0.998 | 1.000 | 1.000 | 11571 | tags=18%, list=21%, signal=23% | |
5746 | BRANCHING INVOLVED IN URETERIC BUD MORPHOGENESIS | 40 | -0.09 | -0.31 | 1.000 | 1.000 | 1.000 | 33291 | tags=45%, list=61%, signal=115% | |
5747 | REGULATION OF TUMOR NECROSIS FACTOR BIOSYNTHETIC PROCESS | 29 | -0.11 | -0.30 | 1.000 | 1.000 | 1.000 | 40173 | tags=66%, list=73%, signal=247% | |
5748 | REGULATION OF CARDIOBLAST DIFFERENTIATION | 19 | -0.11 | -0.30 | 1.000 | 1.000 | 1.000 | 46231 | tags=84%, list=85%, signal=545% | |
5749 | MESONEPHRIC TUBULE MORPHOGENESIS | 45 | -0.09 | -0.29 | 0.996 | 1.000 | 1.000 | 33291 | tags=44%, list=61%, signal=114% | |
5750 | CELLULAR RESPONSE TO PLATELET-DERIVED GROWTH FACTOR STIMULUS | 12 | -0.11 | -0.29 | 1.000 | 1.000 | 1.000 | 11865 | tags=17%, list=22%, signal=21% | |
5751 | CILIARY NEUROTROPHIC FACTOR-MEDIATED SIGNALING PATHWAY | 17 | -0.11 | -0.27 | 1.000 | 1.000 | 1.000 | 13921 | tags=18%, list=25%, signal=24% | |
5752 | REGULATION OF NITRIC-OXIDE SYNTHASE BIOSYNTHETIC PROCESS | 23 | -0.13 | -0.27 | 1.000 | 1.000 | 1.000 | 45146 | tags=91%, list=83%, signal=524% | |
5753 | ENDOCRINE PANCREAS DEVELOPMENT | 73 | -0.06 | -0.26 | 1.000 | 1.000 | 1.000 | 42623 | tags=67%, list=78%, signal=304% | |
5754 | PROTEIN ACTIVATION CASCADE | 162 | -0.07 | -0.24 | 1.000 | 1.000 | 1.000 | 27983 | tags=35%, list=51%, signal=72% |