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 | POSITIVE REGULATION OF MESENCHYMAL CELL PROLIFERATION | Details ... | 35 | -0.27 | 1.000 | 0.000 | 39866 | tags=100%, list=73%, signal=370% | ||
2 | HUMORAL IMMUNE RESPONSE MEDIATED BY CIRCULATING IMMUNOGLOBULIN | Details ... | 84 | -0.22 | 1.000 | 0.000 | 39006 | tags=98%, list=71%, signal=341% | ||
3 | COMPLEMENT ACTIVATION, CLASSICAL PATHWAY | Details ... | 70 | -0.21 | 1.000 | 0.000 | 39006 | tags=97%, list=71%, signal=340% | ||
4 | BICARBONATE TRANSPORT | Details ... | 75 | -0.18 | 1.000 | 0.000 | 40589 | tags=96%, list=74%, signal=373% | ||
5 | NEGATIVE REGULATION OF BLOOD COAGULATION | Details ... | 73 | -0.16 | 1.000 | 0.000 | 36124 | tags=92%, list=66%, signal=271% | ||
6 | PROTEIN O-LINKED FUCOSYLATION | Details ... | 36 | -0.16 | 1.000 | 0.000 | 34218 | tags=89%, list=63%, signal=238% | ||
7 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT5 PROTEIN | Details ... | 50 | -0.17 | 1.000 | 0.000 | 34101 | tags=90%, list=62%, signal=239% | ||
8 | NEGATIVE REGULATION OF COAGULATION | Details ... | 75 | -0.17 | 1.000 | 0.000 | 36124 | tags=92%, list=66%, signal=271% | ||
9 | NEGATIVE REGULATION OF B CELL ACTIVATION | Details ... | 40 | -0.20 | 1.000 | 0.000 | 40466 | tags=98%, list=74%, signal=376% | ||
10 | DETECTION OF STIMULUS INVOLVED IN SENSORY PERCEPTION | Details ... | 81 | -0.14 | 1.000 | 0.000 | 41018 | tags=95%, list=75%, signal=381% | ||
11 | SODIUM ION HOMEOSTASIS | Details ... | 44 | -0.17 | 1.000 | 0.000 | 45215 | tags=100%, list=83%, signal=581% | ||
12 | CHEMOKINE-MEDIATED SIGNALING PATHWAY | Details ... | 42 | -0.15 | 1.000 | 0.000 | 40385 | tags=95%, list=74%, signal=365% | ||
13 | NEGATIVE REGULATION OF HEMOSTASIS | Details ... | 73 | -0.16 | 1.000 | 0.000 | 36124 | tags=92%, list=66%, signal=271% | ||
14 | POSITIVE REGULATION OF CGMP METABOLIC PROCESS | Details ... | 18 | -0.44 | -2.07 | 0.000 | 0.015 | 0.069 | 30593 | tags=100%, list=56%, signal=227% |
15 | ALKALOID METABOLIC PROCESS | Details ... | 20 | -0.41 | -1.83 | 0.000 | 0.079 | 0.331 | 26945 | tags=95%, list=49%, signal=187% |
16 | AMACRINE CELL DIFFERENTIATION | Details ... | 8 | -0.60 | -1.80 | 0.009 | 0.095 | 0.398 | 21898 | tags=100%, list=40%, signal=167% |
17 | CELLULAR RESPONSE TO PLATELET-DERIVED GROWTH FACTOR STIMULUS | Details ... | 12 | -0.47 | -1.77 | 0.000 | 0.114 | 0.481 | 28743 | tags=100%, list=53%, signal=211% |
18 | REGULATION OF ACTIVATION OF JAK2 KINASE ACTIVITY | Details ... | 20 | -0.40 | -1.75 | 0.000 | 0.116 | 0.507 | 32797 | tags=100%, list=60%, signal=250% |
19 | LEUKOCYTE MIGRATION INVOLVED IN INFLAMMATORY RESPONSE | Details ... | 5 | -0.66 | -1.71 | 0.019 | 0.151 | 0.622 | 18361 | tags=100%, list=34%, signal=151% |
20 | POSITIVE REGULATION OF CGMP BIOSYNTHETIC PROCESS | Details ... | 14 | -0.44 | -1.71 | 0.000 | 0.145 | 0.625 | 30593 | tags=100%, list=56%, signal=227% |
21 | DETECTION OF LIGHT STIMULUS INVOLVED IN VISUAL PERCEPTION | 13 | -0.45 | -1.67 | 0.000 | 0.171 | 0.710 | 30050 | tags=100%, list=55%, signal=222% | |
22 | DETECTION OF LIGHT STIMULUS INVOLVED IN SENSORY PERCEPTION | 13 | -0.45 | -1.67 | 0.022 | 0.172 | 0.726 | 30050 | tags=100%, list=55%, signal=222% | |
23 | IMMUNE RESPONSE-INHIBITING SIGNAL TRANSDUCTION | 13 | -0.43 | -1.66 | 0.022 | 0.165 | 0.727 | 31366 | tags=100%, list=57%, signal=235% | |
24 | POSITIVE REGULATION OF GUANYLATE CYCLASE ACTIVITY | 10 | -0.46 | -1.62 | 0.000 | 0.201 | 0.806 | 29514 | tags=100%, list=54%, signal=218% | |
25 | REGULATION OF T-HELPER 17 CELL DIFFERENTIATION | 10 | -0.50 | -1.62 | 0.029 | 0.195 | 0.810 | 27526 | tags=100%, list=50%, signal=202% | |
26 | IMMUNE RESPONSE-INHIBITING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 13 | -0.43 | -1.58 | 0.023 | 0.239 | 0.875 | 31366 | tags=100%, list=57%, signal=235% | |
27 | POSITIVE REGULATION OF ACTIVATION OF JAK2 KINASE ACTIVITY | 17 | -0.40 | -1.56 | 0.000 | 0.265 | 0.905 | 32797 | tags=100%, list=60%, signal=250% | |
28 | CELLULAR RESPONSE TO CAFFEINE | 18 | -0.34 | -1.55 | 0.000 | 0.269 | 0.919 | 35808 | tags=100%, list=66%, signal=290% | |
29 | NEUROTRANSMITTER-GATED ION CHANNEL CLUSTERING | 15 | -0.36 | -1.53 | 0.000 | 0.297 | 0.946 | 35089 | tags=100%, list=64%, signal=280% | |
30 | RESPONSE TO CAFFEINE | 18 | -0.34 | -1.50 | 0.067 | 0.324 | 0.965 | 35808 | tags=100%, list=66%, signal=290% | |
31 | POSITIVE REGULATION OF CELL MIGRATION INVOLVED IN SPROUTING ANGIOGENESIS | 15 | -0.37 | -1.50 | 0.000 | 0.318 | 0.967 | 17785 | tags=87%, list=33%, signal=128% | |
32 | CELLULAR RESPONSE TO PURINE-CONTAINING COMPOUND | 18 | -0.34 | -1.50 | 0.045 | 0.315 | 0.970 | 35808 | tags=100%, list=66%, signal=290% | |
33 | VASCULAR ENDOTHELIAL GROWTH FACTOR SIGNALING PATHWAY | 35 | -0.20 | -1.49 | 0.000 | 0.316 | 0.976 | 43955 | tags=100%, list=80%, signal=512% | |
34 | INTERLEUKIN-1 BETA SECRETION | 22 | -0.29 | -1.49 | 0.111 | 0.311 | 0.976 | 38596 | tags=100%, list=71%, signal=341% | |
35 | LIPOXYGENASE PATHWAY | 19 | -0.36 | -1.49 | 0.045 | 0.308 | 0.978 | 34967 | tags=100%, list=64%, signal=278% | |
36 | STAT PROTEIN IMPORT INTO NUCLEUS | 13 | -0.37 | -1.46 | 0.019 | 0.339 | 0.984 | 34248 | tags=100%, list=63%, signal=268% | |
37 | SENSORY PERCEPTION OF TEMPERATURE STIMULUS | 10 | -0.43 | -1.43 | 0.073 | 0.396 | 0.992 | 31142 | tags=100%, list=57%, signal=233% | |
38 | CANNABINOID SIGNALING PATHWAY | 7 | -0.49 | -1.42 | 0.087 | 0.407 | 0.993 | 27875 | tags=100%, list=51%, signal=204% | |
39 | SKELETAL MUSCLE THIN FILAMENT ASSEMBLY | 11 | -0.41 | -1.41 | 0.094 | 0.426 | 0.995 | 18764 | tags=91%, list=34%, signal=138% | |
40 | ACTIVATION OF TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE ACTIVITY | 24 | -0.26 | -1.40 | 0.000 | 0.447 | 0.996 | 40511 | tags=100%, list=74%, signal=387% | |
41 | HEPOXILIN METABOLIC PROCESS | 7 | -0.47 | -1.40 | 0.070 | 0.441 | 0.996 | 28922 | tags=100%, list=53%, signal=213% | |
42 | POSITIVE REGULATION OF PROTEIN KINASE A SIGNALING | 10 | -0.38 | -1.39 | 0.040 | 0.456 | 0.996 | 33852 | tags=100%, list=62%, signal=263% | |
43 | POSITIVE REGULATION OF ACTIVATION OF JANUS KINASE ACTIVITY | 20 | -0.29 | -1.38 | 0.067 | 0.455 | 0.997 | 32797 | tags=95%, list=60%, signal=238% | |
44 | NEGATIVE REGULATION OF PLATELET AGGREGATION | 12 | -0.36 | -1.37 | 0.094 | 0.488 | 0.998 | 35008 | tags=100%, list=64%, signal=279% | |
45 | EQUILIBRIOCEPTION | 17 | -0.32 | -1.36 | 0.033 | 0.494 | 0.998 | 29864 | tags=94%, list=55%, signal=208% | |
46 | CELL PROLIFERATION INVOLVED IN KIDNEY DEVELOPMENT | 13 | -0.35 | -1.35 | 0.106 | 0.493 | 1.000 | 35484 | tags=100%, list=65%, signal=285% | |
47 | POSITIVE REGULATION OF ACUTE INFLAMMATORY RESPONSE | 24 | -0.25 | -1.35 | 0.000 | 0.493 | 1.000 | 40885 | tags=100%, list=75%, signal=398% | |
48 | NEURONAL SIGNAL TRANSDUCTION | 15 | -0.36 | -1.35 | 0.097 | 0.485 | 1.000 | 35089 | tags=100%, list=64%, signal=280% | |
49 | REGULATION OF CGMP METABOLIC PROCESS | 32 | -0.26 | -1.34 | 0.000 | 0.497 | 1.000 | 30593 | tags=91%, list=56%, signal=206% | |
50 | HEPOXILIN BIOSYNTHETIC PROCESS | 7 | -0.47 | -1.34 | 0.109 | 0.500 | 1.000 | 28922 | tags=100%, list=53%, signal=213% | |
51 | POSITIVE REGULATION OF CHOLESTEROL ESTERIFICATION | 13 | -0.34 | -1.33 | 0.051 | 0.512 | 1.000 | 36213 | tags=100%, list=66%, signal=297% | |
52 | ACYLGLYCEROL ACYL-CHAIN REMODELING | 10 | -0.39 | -1.32 | 0.125 | 0.516 | 1.000 | 33530 | tags=100%, list=61%, signal=259% | |
53 | INTERLEUKIN-1 BETA PRODUCTION | 23 | -0.29 | -1.32 | 0.111 | 0.527 | 1.000 | 38596 | tags=100%, list=71%, signal=341% | |
54 | REGULATION OF ACTIVATION OF JANUS KINASE ACTIVITY | 23 | -0.29 | -1.31 | 0.000 | 0.533 | 1.000 | 32797 | tags=96%, list=60%, signal=239% | |
55 | REGULATION OF CGMP BIOSYNTHETIC PROCESS | 16 | -0.32 | -1.30 | 0.118 | 0.543 | 1.000 | 30593 | tags=94%, list=56%, signal=213% | |
56 | REGULATION OF CELL MATURATION | 9 | -0.39 | -1.30 | 0.115 | 0.552 | 1.000 | 33178 | tags=100%, list=61%, signal=255% | |
57 | INTERLEUKIN-1 PRODUCTION | 25 | -0.26 | -1.30 | 0.111 | 0.546 | 1.000 | 40328 | tags=100%, list=74%, signal=382% | |
58 | HISTIDINE CATABOLIC PROCESS | 19 | -0.26 | -1.29 | 0.083 | 0.545 | 1.000 | 40372 | tags=100%, list=74%, signal=383% | |
59 | POSITIVE REGULATION OF NATURAL KILLER CELL MEDIATED CYTOTOXICITY DIRECTED AGAINST TUMOR CELL TARGET | 15 | -0.32 | -1.29 | 0.097 | 0.546 | 1.000 | 37326 | tags=100%, list=68%, signal=316% | |
60 | KILLING OF CELLS OF OTHER ORGANISM | 8 | -0.40 | -1.28 | 0.133 | 0.553 | 1.000 | 20009 | tags=88%, list=37%, signal=138% | |
61 | NEGATIVE REGULATION OF LIPOPROTEIN METABOLIC PROCESS | 13 | -0.34 | -1.28 | 0.150 | 0.559 | 1.000 | 25581 | tags=92%, list=47%, signal=174% | |
62 | EPOXYGENASE P450 PATHWAY | 26 | -0.28 | -1.27 | 0.000 | 0.567 | 1.000 | 39151 | tags=100%, list=72%, signal=353% | |
63 | HEMATOPOIETIC STEM CELL DIFFERENTIATION | 8 | -0.40 | -1.26 | 0.155 | 0.596 | 1.000 | 32527 | tags=100%, list=60%, signal=247% | |
64 | T CELL CHEMOTAXIS | 10 | -0.37 | -1.25 | 0.165 | 0.604 | 1.000 | 34451 | tags=100%, list=63%, signal=271% | |
65 | MIDDLE EAR MORPHOGENESIS | 9 | -0.40 | -1.25 | 0.144 | 0.603 | 1.000 | 32569 | tags=100%, list=60%, signal=248% | |
66 | MESENCHYMAL CELL PROLIFERATION | 26 | -0.27 | -1.25 | 0.222 | 0.594 | 1.000 | 35484 | tags=96%, list=65%, signal=274% | |
67 | REGULATION OF NATURAL KILLER CELL MEDIATED CYTOTOXICITY DIRECTED AGAINST TUMOR CELL TARGET | 15 | -0.32 | -1.25 | 0.122 | 0.589 | 1.000 | 37326 | tags=100%, list=68%, signal=316% | |
68 | REGULATION OF CYTOKINE SECRETION INVOLVED IN IMMUNE RESPONSE | 13 | -0.34 | -1.25 | 0.186 | 0.587 | 1.000 | 36213 | tags=100%, list=66%, signal=297% | |
69 | MINERALOCORTICOID BIOSYNTHETIC PROCESS | 9 | -0.37 | -1.24 | 0.177 | 0.586 | 1.000 | 34292 | tags=100%, list=63%, signal=269% | |
70 | POSITIVE REGULATION OF NATURAL KILLER CELL MEDIATED IMMUNE RESPONSE TO TUMOR CELL | 15 | -0.32 | -1.24 | 0.132 | 0.581 | 1.000 | 37326 | tags=100%, list=68%, signal=316% | |
71 | REGULATION OF NLRP3 INFLAMMASOME COMPLEX ASSEMBLY | 17 | -0.29 | -1.24 | 0.171 | 0.575 | 1.000 | 32233 | tags=94%, list=59%, signal=230% | |
72 | REGULATION OF BONE DEVELOPMENT | 7 | -0.43 | -1.24 | 0.175 | 0.568 | 1.000 | 31311 | tags=100%, list=57%, signal=234% | |
73 | CEREBELLAR GRANULAR LAYER DEVELOPMENT | 15 | -0.28 | -1.23 | 0.073 | 0.591 | 1.000 | 32725 | tags=93%, list=60%, signal=233% | |
74 | DISRUPTION OF CELLS OF OTHER ORGANISM | 8 | -0.40 | -1.23 | 0.194 | 0.585 | 1.000 | 20009 | tags=88%, list=37%, signal=138% | |
75 | MINERALOCORTICOID METABOLIC PROCESS | 9 | -0.37 | -1.22 | 0.200 | 0.603 | 1.000 | 34292 | tags=100%, list=63%, signal=269% | |
76 | IMIDAZOLE-CONTAINING COMPOUND CATABOLIC PROCESS | 19 | -0.26 | -1.22 | 0.188 | 0.596 | 1.000 | 40372 | tags=100%, list=74%, signal=383% | |
77 | RESPONSE TO PLATELET-DERIVED GROWTH FACTOR | 15 | -0.29 | -1.22 | 0.094 | 0.600 | 1.000 | 28743 | tags=93%, list=53%, signal=197% | |
78 | REGULATION OF NATURAL KILLER CELL MEDIATED IMMUNE RESPONSE TO TUMOR CELL | 15 | -0.32 | -1.22 | 0.130 | 0.595 | 1.000 | 37326 | tags=100%, list=68%, signal=316% | |
79 | HISTIDINE METABOLIC PROCESS | 19 | -0.26 | -1.22 | 0.176 | 0.592 | 1.000 | 40372 | tags=100%, list=74%, signal=383% | |
80 | NEGATIVE REGULATION OF INTERLEUKIN-17 PRODUCTION | 15 | -0.29 | -1.22 | 0.091 | 0.590 | 1.000 | 38884 | tags=100%, list=71%, signal=347% | |
81 | REGULATION OF OOCYTE DEVELOPMENT | 8 | -0.39 | -1.21 | 0.180 | 0.597 | 1.000 | 33178 | tags=100%, list=61%, signal=255% | |
82 | GAS TRANSPORT | 18 | -0.29 | -1.21 | 0.179 | 0.591 | 1.000 | 23961 | tags=83%, list=44%, signal=148% | |
83 | REGULATION OF INTERLEUKIN-2 BIOSYNTHETIC PROCESS | 13 | -0.32 | -1.21 | 0.185 | 0.585 | 1.000 | 37269 | tags=100%, list=68%, signal=315% | |
84 | CELL DIFFERENTIATION IN SPINAL CORD | 31 | -0.22 | -1.21 | 0.000 | 0.588 | 1.000 | 31624 | tags=90%, list=58%, signal=214% | |
85 | CORONARY VASCULATURE MORPHOGENESIS | 16 | -0.29 | -1.19 | 0.091 | 0.618 | 1.000 | 39019 | tags=100%, list=71%, signal=350% | |
86 | INTERLEUKIN-1 SECRETION | 24 | -0.26 | -1.19 | 0.200 | 0.628 | 1.000 | 40328 | tags=100%, list=74%, signal=382% | |
87 | SPINAL CORD PATTERNING | 14 | -0.30 | -1.18 | 0.238 | 0.635 | 1.000 | 30837 | tags=93%, list=56%, signal=213% | |
88 | REGULATION OF MACROPHAGE CYTOKINE PRODUCTION | 15 | -0.30 | -1.18 | 0.154 | 0.637 | 1.000 | 32559 | tags=93%, list=60%, signal=231% | |
89 | G-PROTEIN COUPLED PURINERGIC RECEPTOR SIGNALING PATHWAY | 5 | -0.46 | -1.17 | 0.229 | 0.655 | 1.000 | 29671 | tags=100%, list=54%, signal=219% | |
90 | POSITIVE REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 35 | -0.20 | -1.17 | 0.000 | 0.656 | 1.000 | 43551 | tags=100%, list=80%, signal=493% | |
91 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT5 PROTEIN | 36 | -0.26 | -1.17 | 0.000 | 0.663 | 1.000 | 33425 | tags=94%, list=61%, signal=243% | |
92 | POSITIVE REGULATION OF OSTEOBLAST PROLIFERATION | 9 | -0.35 | -1.16 | 0.208 | 0.682 | 1.000 | 35329 | tags=100%, list=65%, signal=283% | |
93 | ADULT FEEDING BEHAVIOR | 10 | -0.34 | -1.16 | 0.280 | 0.678 | 1.000 | 36188 | tags=100%, list=66%, signal=296% | |
94 | ADULT HEART DEVELOPMENT | 10 | -0.35 | -1.16 | 0.238 | 0.674 | 1.000 | 35694 | tags=100%, list=65%, signal=289% | |
95 | POSITIVE REGULATION OF SMOOTHENED SIGNALING PATHWAY | 19 | -0.25 | -1.14 | 0.250 | 0.714 | 1.000 | 35513 | tags=95%, list=65%, signal=271% | |
96 | PERICARDIUM DEVELOPMENT | 14 | -0.30 | -1.13 | 0.205 | 0.756 | 1.000 | 38473 | tags=100%, list=70%, signal=338% | |
97 | REGULATION OF EXCRETION | 12 | -0.29 | -1.13 | 0.196 | 0.754 | 1.000 | 38744 | tags=100%, list=71%, signal=344% | |
98 | ESTROGEN BIOSYNTHETIC PROCESS | 12 | -0.30 | -1.12 | 0.268 | 0.753 | 1.000 | 25766 | tags=92%, list=47%, signal=174% | |
99 | POSITIVE REGULATION OF DEFENSE RESPONSE TO BACTERIUM | 10 | -0.34 | -1.12 | 0.290 | 0.749 | 1.000 | 36209 | tags=100%, list=66%, signal=297% | |
100 | COMPLEMENT ACTIVATION, LECTIN PATHWAY | 15 | -0.27 | -1.12 | 0.242 | 0.752 | 1.000 | 33028 | tags=93%, list=60%, signal=236% | |
101 | POSITIVE REGULATION OF CORTICOSTEROID HORMONE SECRETION | 9 | -0.34 | -1.12 | 0.316 | 0.754 | 1.000 | 36188 | tags=100%, list=66%, signal=296% | |
102 | INDOLALKYLAMINE CATABOLIC PROCESS | 19 | -0.25 | -1.11 | 0.294 | 0.763 | 1.000 | 34494 | tags=95%, list=63%, signal=257% | |
103 | REGULATION OF CELL-CELL ADHESION MEDIATED BY INTEGRIN | 14 | -0.28 | -1.11 | 0.300 | 0.769 | 1.000 | 31159 | tags=93%, list=57%, signal=216% | |
104 | NEGATIVE REGULATION OF OSTEOBLAST PROLIFERATION | 14 | -0.28 | -1.11 | 0.353 | 0.765 | 1.000 | 39265 | tags=100%, list=72%, signal=356% | |
105 | NEGATIVE REGULATION OF HUMORAL IMMUNE RESPONSE | 23 | -0.24 | -1.11 | 0.167 | 0.765 | 1.000 | 41516 | tags=100%, list=76%, signal=417% | |
106 | HIGH-DENSITY LIPOPROTEIN PARTICLE ASSEMBLY | 14 | -0.29 | -1.11 | 0.367 | 0.760 | 1.000 | 38596 | tags=100%, list=71%, signal=341% | |
107 | IMIDAZOLE-CONTAINING COMPOUND METABOLIC PROCESS | 20 | -0.26 | -1.10 | 0.263 | 0.759 | 1.000 | 40372 | tags=100%, list=74%, signal=383% | |
108 | IMMUNOLOGICAL SYNAPSE FORMATION | 12 | -0.30 | -1.10 | 0.279 | 0.756 | 1.000 | 38371 | tags=100%, list=70%, signal=336% | |
109 | SPINAL CORD DORSAL/VENTRAL PATTERNING | 13 | -0.30 | -1.10 | 0.231 | 0.754 | 1.000 | 30837 | tags=92%, list=56%, signal=212% | |
110 | INDOLE-CONTAINING COMPOUND CATABOLIC PROCESS | 19 | -0.25 | -1.10 | 0.278 | 0.766 | 1.000 | 34494 | tags=95%, list=63%, signal=257% | |
111 | RENAL ABSORPTION | 23 | -0.23 | -1.09 | 0.375 | 0.769 | 1.000 | 33479 | tags=91%, list=61%, signal=236% | |
112 | TRYPTOPHAN CATABOLIC PROCESS | 19 | -0.25 | -1.09 | 0.273 | 0.780 | 1.000 | 34494 | tags=95%, list=63%, signal=257% | |
113 | MALE GENITALIA DEVELOPMENT | 13 | -0.29 | -1.09 | 0.345 | 0.783 | 1.000 | 38874 | tags=100%, list=71%, signal=347% | |
114 | REGULATION OF GUANYLATE CYCLASE ACTIVITY | 12 | -0.30 | -1.08 | 0.281 | 0.782 | 1.000 | 29514 | tags=92%, list=54%, signal=199% | |
115 | AXIS ELONGATION | 18 | -0.27 | -1.08 | 0.160 | 0.785 | 1.000 | 39866 | tags=100%, list=73%, signal=370% | |
116 | POSITIVE REGULATION OF GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR PRODUCTION | 10 | -0.31 | -1.08 | 0.301 | 0.780 | 1.000 | 37516 | tags=100%, list=69%, signal=319% | |
117 | GLYCEROL TRANSPORT | 9 | -0.33 | -1.07 | 0.364 | 0.793 | 1.000 | 23961 | tags=89%, list=44%, signal=158% | |
118 | POSITIVE REGULATION OF FEVER GENERATION | 15 | -0.25 | -1.07 | 0.344 | 0.791 | 1.000 | 40885 | tags=100%, list=75%, signal=398% | |
119 | VENOUS BLOOD VESSEL MORPHOGENESIS | 15 | -0.27 | -1.07 | 0.273 | 0.788 | 1.000 | 40120 | tags=100%, list=73%, signal=377% | |
120 | POSITIVE REGULATION OF TOLERANCE INDUCTION | 12 | -0.29 | -1.06 | 0.288 | 0.807 | 1.000 | 31761 | tags=92%, list=58%, signal=219% | |
121 | RESPONSE TO VITAMIN D | 21 | -0.23 | -1.06 | 0.467 | 0.802 | 1.000 | 42228 | tags=100%, list=77%, signal=441% | |
122 | POLYSACCHARIDE DIGESTION | 5 | -0.42 | -1.06 | 0.350 | 0.814 | 1.000 | 31821 | tags=100%, list=58%, signal=240% | |
123 | COLLECTING DUCT DEVELOPMENT | 13 | -0.26 | -1.06 | 0.340 | 0.808 | 1.000 | 40377 | tags=100%, list=74%, signal=384% | |
124 | PATTERNING OF BLOOD VESSELS | 22 | -0.23 | -1.06 | 0.385 | 0.803 | 1.000 | 41820 | tags=100%, list=77%, signal=427% | |
125 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION | 45 | -0.20 | -1.05 | 0.000 | 0.817 | 1.000 | 41018 | tags=98%, list=75%, signal=393% | |
126 | INDOLE-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 9 | -0.32 | -1.05 | 0.348 | 0.813 | 1.000 | 37411 | tags=100%, list=69%, signal=317% | |
127 | PURKINJE MYOCYTE TO VENTRICULAR CARDIAC MUSCLE CELL COMMUNICATION | 4 | -0.46 | -1.05 | 0.379 | 0.819 | 1.000 | 29331 | tags=100%, list=54%, signal=216% | |
128 | BONE RESORPTION | 19 | -0.24 | -1.04 | 0.375 | 0.829 | 1.000 | 41409 | tags=100%, list=76%, signal=414% | |
129 | PHOSPHOLIPID HOMEOSTASIS | 22 | -0.21 | -1.04 | 0.333 | 0.826 | 1.000 | 31820 | tags=91%, list=58%, signal=218% | |
130 | PARTURITION | 13 | -0.27 | -1.04 | 0.421 | 0.827 | 1.000 | 39848 | tags=100%, list=73%, signal=370% | |
131 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION INVOLVED IN INFLAMMATORY RESPONSE | 5 | -0.41 | -1.04 | 0.383 | 0.821 | 1.000 | 31992 | tags=100%, list=59%, signal=241% | |
132 | AMELOGENESIS | 27 | -0.21 | -1.04 | 0.333 | 0.818 | 1.000 | 43272 | tags=100%, list=79%, signal=481% | |
133 | REGULATION OF CORTICOSTEROID HORMONE SECRETION | 12 | -0.27 | -1.04 | 0.379 | 0.812 | 1.000 | 39848 | tags=100%, list=73%, signal=370% | |
134 | INDOLALKYLAMINE BIOSYNTHETIC PROCESS | 9 | -0.32 | -1.04 | 0.341 | 0.810 | 1.000 | 37411 | tags=100%, list=69%, signal=317% | |
135 | POSITIVE REGULATION OF ANTIMICROBIAL HUMORAL RESPONSE | 7 | -0.35 | -1.03 | 0.378 | 0.808 | 1.000 | 35550 | tags=100%, list=65%, signal=286% | |
136 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION OF TASTE | 36 | -0.22 | -1.03 | 0.500 | 0.807 | 1.000 | 39166 | tags=97%, list=72%, signal=344% | |
137 | REGULATION OF FEVER GENERATION | 15 | -0.25 | -1.03 | 0.407 | 0.802 | 1.000 | 40885 | tags=100%, list=75%, signal=398% | |
138 | TRIGLYCERIDE-RICH LIPOPROTEIN PARTICLE CLEARANCE | 12 | -0.26 | -1.03 | 0.390 | 0.806 | 1.000 | 31542 | tags=92%, list=58%, signal=217% | |
139 | CGMP-MEDIATED SIGNALING | 17 | -0.25 | -1.03 | 0.424 | 0.804 | 1.000 | 32233 | tags=94%, list=59%, signal=230% | |
140 | MONOAMINE TRANSPORT | 25 | -0.21 | -1.03 | 0.500 | 0.803 | 1.000 | 22819 | tags=80%, list=42%, signal=137% | |
141 | PURKINJE MYOCYTE TO VENTRICULAR CARDIAC MUSCLE CELL SIGNALING | 4 | -0.46 | -1.02 | 0.425 | 0.826 | 1.000 | 29331 | tags=100%, list=54%, signal=216% | |
142 | LEUKOTRIENE B4 METABOLIC PROCESS | 7 | -0.34 | -1.01 | 0.413 | 0.837 | 1.000 | 36163 | tags=100%, list=66%, signal=296% | |
143 | POSITIVE REGULATION OF HEAT GENERATION | 15 | -0.25 | -1.01 | 0.400 | 0.833 | 1.000 | 40885 | tags=100%, list=75%, signal=398% | |
144 | REGULATION OF MALE GONAD DEVELOPMENT | 12 | -0.27 | -1.01 | 0.473 | 0.854 | 1.000 | 39807 | tags=100%, list=73%, signal=369% | |
145 | REGULATION OF RENAL SODIUM EXCRETION | 9 | -0.29 | -1.01 | 0.465 | 0.849 | 1.000 | 38744 | tags=100%, list=71%, signal=344% | |
146 | CYTOLYSIS | 9 | -0.30 | -1.00 | 0.481 | 0.849 | 1.000 | 38273 | tags=100%, list=70%, signal=334% | |
147 | EYE PHOTORECEPTOR CELL DEVELOPMENT | 18 | -0.24 | -1.00 | 0.579 | 0.843 | 1.000 | 41289 | tags=100%, list=76%, signal=410% | |
148 | VERY-LOW-DENSITY LIPOPROTEIN PARTICLE REMODELING | 14 | -0.26 | -1.00 | 0.435 | 0.841 | 1.000 | 31542 | tags=93%, list=58%, signal=220% | |
149 | REGULATION OF ANTIMICROBIAL HUMORAL RESPONSE | 7 | -0.35 | -1.00 | 0.421 | 0.837 | 1.000 | 35550 | tags=100%, list=65%, signal=286% | |
150 | NEGATIVE REGULATION OF CYTOKINE SECRETION INVOLVED IN IMMUNE RESPONSE | 8 | -0.34 | -1.00 | 0.510 | 0.832 | 1.000 | 36213 | tags=100%, list=66%, signal=297% | |
151 | POSITIVE REGULATION OF INTERLEUKIN-2 BIOSYNTHETIC PROCESS | 8 | -0.32 | -1.00 | 0.426 | 0.827 | 1.000 | 37269 | tags=100%, list=68%, signal=315% | |
152 | RESPONSE TO MANGANESE ION | 9 | -0.30 | -1.00 | 0.412 | 0.838 | 1.000 | 29252 | tags=89%, list=54%, signal=191% | |
153 | GLYCINE TRANSPORT | 7 | -0.34 | -1.00 | 0.432 | 0.833 | 1.000 | 36020 | tags=100%, list=66%, signal=294% | |
154 | POSITIVE REGULATION OF VASOCONSTRICTION | 15 | -0.26 | -1.00 | 0.564 | 0.829 | 1.000 | 33757 | tags=93%, list=62%, signal=244% | |
155 | ENDOTHELIAL CELL CHEMOTAXIS | 20 | -0.22 | -1.00 | 0.667 | 0.828 | 1.000 | 31548 | tags=90%, list=58%, signal=213% | |
156 | REGULATION OF CHOLESTEROL ESTERIFICATION | 17 | -0.23 | -1.00 | 0.565 | 0.823 | 1.000 | 36213 | tags=94%, list=66%, signal=279% | |
157 | CHOLESTEROL CATABOLIC PROCESS | 6 | -0.35 | -1.00 | 0.453 | 0.819 | 1.000 | 35345 | tags=100%, list=65%, signal=283% | |
158 | REGULATION OF PLASMINOGEN ACTIVATION | 21 | -0.22 | -0.99 | 0.500 | 0.816 | 1.000 | 36947 | tags=95%, list=68%, signal=294% | |
159 | REGULATION OF TUMOR NECROSIS FACTOR BIOSYNTHETIC PROCESS | 29 | -0.21 | -0.99 | 0.500 | 0.813 | 1.000 | 38528 | tags=97%, list=71%, signal=328% | |
160 | DEFENSE RESPONSE TO PROTOZOAN | 15 | -0.24 | -0.99 | 0.442 | 0.820 | 1.000 | 34537 | tags=93%, list=63%, signal=254% | |
161 | ICOSANOID CATABOLIC PROCESS | 7 | -0.34 | -0.99 | 0.481 | 0.817 | 1.000 | 36163 | tags=100%, list=66%, signal=296% | |
162 | REGULATION OF HEAT GENERATION | 15 | -0.25 | -0.99 | 0.512 | 0.815 | 1.000 | 40885 | tags=100%, list=75%, signal=398% | |
163 | CHYLOMICRON REMNANT CLEARANCE | 12 | -0.26 | -0.99 | 0.492 | 0.818 | 1.000 | 31542 | tags=92%, list=58%, signal=217% | |
164 | NEGATIVE REGULATION OF FERTILIZATION | 4 | -0.45 | -0.99 | 0.459 | 0.813 | 1.000 | 30046 | tags=100%, list=55%, signal=222% | |
165 | LEUKOTRIENE B4 CATABOLIC PROCESS | 7 | -0.34 | -0.98 | 0.456 | 0.810 | 1.000 | 36163 | tags=100%, list=66%, signal=296% | |
166 | REGULATION OF CHEMOKINE BIOSYNTHETIC PROCESS | 9 | -0.31 | -0.98 | 0.516 | 0.811 | 1.000 | 37741 | tags=100%, list=69%, signal=324% | |
167 | FATTY ACID DERIVATIVE CATABOLIC PROCESS | 7 | -0.34 | -0.98 | 0.456 | 0.810 | 1.000 | 36163 | tags=100%, list=66%, signal=296% | |
168 | DOPAMINE BIOSYNTHETIC PROCESS | 13 | -0.25 | -0.97 | 0.554 | 0.832 | 1.000 | 41001 | tags=100%, list=75%, signal=401% | |
169 | STEROL CATABOLIC PROCESS | 6 | -0.35 | -0.97 | 0.507 | 0.827 | 1.000 | 35345 | tags=100%, list=65%, signal=283% | |
170 | CEREBELLAR GRANULAR LAYER MORPHOGENESIS | 13 | -0.27 | -0.97 | 0.450 | 0.825 | 1.000 | 40120 | tags=100%, list=73%, signal=377% | |
171 | RETINA VASCULATURE MORPHOGENESIS IN CAMERA-TYPE EYE | 14 | -0.24 | -0.97 | 0.639 | 0.821 | 1.000 | 41309 | tags=100%, list=76%, signal=410% | |
172 | CELL MIGRATION INVOLVED IN HEART DEVELOPMENT | 13 | -0.25 | -0.97 | 0.510 | 0.816 | 1.000 | 40959 | tags=100%, list=75%, signal=400% | |
173 | FAT-SOLUBLE VITAMIN BIOSYNTHETIC PROCESS | 9 | -0.30 | -0.97 | 0.511 | 0.812 | 1.000 | 38374 | tags=100%, list=70%, signal=336% | |
174 | LIPOXIN METABOLIC PROCESS | 15 | -0.24 | -0.97 | 0.568 | 0.810 | 1.000 | 34967 | tags=93%, list=64%, signal=259% | |
175 | VENTRAL SPINAL CORD DEVELOPMENT | 24 | -0.21 | -0.97 | 0.545 | 0.811 | 1.000 | 30837 | tags=88%, list=56%, signal=201% | |
176 | SEROTONIN RECEPTOR SIGNALING PATHWAY | 23 | -0.22 | -0.97 | 0.533 | 0.814 | 1.000 | 37780 | tags=96%, list=69%, signal=310% | |
177 | LEUKOTRIENE CATABOLIC PROCESS | 7 | -0.34 | -0.96 | 0.479 | 0.826 | 1.000 | 36163 | tags=100%, list=66%, signal=296% | |
178 | LATERAL MESODERM DEVELOPMENT | 11 | -0.27 | -0.95 | 0.486 | 0.835 | 1.000 | 39807 | tags=100%, list=73%, signal=369% | |
179 | ATRIOVENTRICULAR CANAL DEVELOPMENT | 18 | -0.24 | -0.95 | 0.565 | 0.838 | 1.000 | 35496 | tags=94%, list=65%, signal=270% | |
180 | VITAMIN BIOSYNTHETIC PROCESS | 9 | -0.30 | -0.95 | 0.570 | 0.840 | 1.000 | 38374 | tags=100%, list=70%, signal=336% | |
181 | RESPONSE TO PROTOZOAN | 15 | -0.24 | -0.95 | 0.564 | 0.847 | 1.000 | 34537 | tags=93%, list=63%, signal=254% | |
182 | BLEB ASSEMBLY | 18 | -0.22 | -0.94 | 0.522 | 0.846 | 1.000 | 35876 | tags=94%, list=66%, signal=275% | |
183 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION OF BITTER TASTE | 31 | -0.21 | -0.94 | 0.500 | 0.845 | 1.000 | 39166 | tags=97%, list=72%, signal=342% | |
184 | ONE-CARBON COMPOUND TRANSPORT | 9 | -0.28 | -0.94 | 0.526 | 0.843 | 1.000 | 39076 | tags=100%, list=72%, signal=351% | |
185 | NEGATIVE REGULATION OF CARDIAC MUSCLE CELL APOPTOTIC PROCESS | 8 | -0.30 | -0.94 | 0.500 | 0.842 | 1.000 | 38205 | tags=100%, list=70%, signal=333% | |
186 | MATURE B CELL DIFFERENTIATION INVOLVED IN IMMUNE RESPONSE | 15 | -0.24 | -0.94 | 0.500 | 0.843 | 1.000 | 41407 | tags=100%, list=76%, signal=413% | |
187 | NEGATIVE REGULATION OF NITRIC OXIDE METABOLIC PROCESS | 14 | -0.24 | -0.94 | 0.486 | 0.846 | 1.000 | 20216 | tags=79%, list=37%, signal=125% | |
188 | POSITIVE REGULATION OF INSULIN-LIKE GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 23 | -0.20 | -0.94 | 0.563 | 0.842 | 1.000 | 36879 | tags=96%, list=68%, signal=294% | |
189 | REGULATION OF NATURAL KILLER CELL PROLIFERATION | 8 | -0.31 | -0.93 | 0.566 | 0.843 | 1.000 | 37516 | tags=100%, list=69%, signal=319% | |
190 | SNRNA TRANSCRIPTION FROM RNA POLYMERASE III PROMOTER | 6 | -0.34 | -0.93 | 0.546 | 0.845 | 1.000 | 36078 | tags=100%, list=66%, signal=295% | |
191 | REGULATION OF ALDOSTERONE BIOSYNTHETIC PROCESS | 17 | -0.21 | -0.93 | 0.517 | 0.845 | 1.000 | 36646 | tags=94%, list=67%, signal=286% | |
192 | RESPONSE TO POTASSIUM ION | 8 | -0.30 | -0.93 | 0.556 | 0.843 | 1.000 | 38004 | tags=100%, list=70%, signal=329% | |
193 | BLOOD COAGULATION, EXTRINSIC PATHWAY | 10 | -0.26 | -0.93 | 0.582 | 0.845 | 1.000 | 31887 | tags=90%, list=58%, signal=216% | |
194 | MARGINAL ZONE B CELL DIFFERENTIATION | 14 | -0.24 | -0.92 | 0.514 | 0.844 | 1.000 | 41407 | tags=100%, list=76%, signal=413% | |
195 | CELLULAR RESPONSE TO POTASSIUM ION | 8 | -0.30 | -0.92 | 0.593 | 0.843 | 1.000 | 38004 | tags=100%, list=70%, signal=329% | |
196 | REGULATION OF GLUCOCORTICOID METABOLIC PROCESS | 17 | -0.21 | -0.92 | 0.593 | 0.842 | 1.000 | 37098 | tags=94%, list=68%, signal=293% | |
197 | LENS FIBER CELL DEVELOPMENT | 10 | -0.27 | -0.92 | 0.557 | 0.839 | 1.000 | 40133 | tags=100%, list=73%, signal=377% | |
198 | MATURE B CELL DIFFERENTIATION | 15 | -0.24 | -0.92 | 0.649 | 0.838 | 1.000 | 41407 | tags=100%, list=76%, signal=413% | |
199 | REGULATION OF GLUCOCORTICOID SECRETION | 10 | -0.27 | -0.92 | 0.696 | 0.847 | 1.000 | 39848 | tags=100%, list=73%, signal=370% | |
200 | REGULATION OF INTERFERON-GAMMA SECRETION | 14 | -0.22 | -0.91 | 0.600 | 0.849 | 1.000 | 33615 | tags=93%, list=62%, signal=241% | |
201 | SODIUM-DEPENDENT PHOSPHATE TRANSPORT | 8 | -0.28 | -0.91 | 0.610 | 0.849 | 1.000 | 39516 | tags=100%, list=72%, signal=362% | |
202 | EOSINOPHIL MIGRATION | 12 | -0.25 | -0.91 | 0.541 | 0.852 | 1.000 | 32155 | tags=92%, list=59%, signal=223% | |
203 | NEGATIVE REGULATION OF NITRIC OXIDE BIOSYNTHETIC PROCESS | 14 | -0.24 | -0.91 | 0.522 | 0.857 | 1.000 | 20216 | tags=79%, list=37%, signal=125% | |
204 | TYPE B PANCREATIC CELL DIFFERENTIATION | 21 | -0.20 | -0.90 | 0.684 | 0.854 | 1.000 | 38482 | tags=95%, list=70%, signal=322% | |
205 | SMAD PROTEIN IMPORT INTO NUCLEUS | 14 | -0.23 | -0.90 | 0.659 | 0.851 | 1.000 | 41874 | tags=100%, list=77%, signal=429% | |
206 | ENTEROENDOCRINE CELL DIFFERENTIATION | 25 | -0.18 | -0.90 | 0.778 | 0.862 | 1.000 | 44546 | tags=100%, list=82%, signal=542% | |
207 | TACHYKININ RECEPTOR SIGNALING PATHWAY | 13 | -0.23 | -0.90 | 0.568 | 0.859 | 1.000 | 25147 | tags=85%, list=46%, signal=157% | |
208 | REGULATION OF N-METHYL-D-ASPARTATE SELECTIVE GLUTAMATE RECEPTOR ACTIVITY | 27 | -0.19 | -0.90 | 0.667 | 0.860 | 1.000 | 30003 | tags=85%, list=55%, signal=189% | |
209 | MYOTUBE CELL DEVELOPMENT | 13 | -0.23 | -0.89 | 0.654 | 0.858 | 1.000 | 34013 | tags=92%, list=62%, signal=245% | |
210 | TRANSCRIPTION, RNA-TEMPLATED | 2 | -0.53 | -0.89 | 0.626 | 0.857 | 1.000 | 25482 | tags=100%, list=47%, signal=187% | |
211 | REGULATION OF ALDOSTERONE METABOLIC PROCESS | 17 | -0.21 | -0.89 | 0.688 | 0.855 | 1.000 | 36646 | tags=94%, list=67%, signal=286% | |
212 | REGULATION OF STEROID HORMONE BIOSYNTHETIC PROCESS | 17 | -0.21 | -0.89 | 0.765 | 0.855 | 1.000 | 36646 | tags=94%, list=67%, signal=286% | |
213 | EOSINOPHIL CHEMOTAXIS | 12 | -0.25 | -0.89 | 0.660 | 0.853 | 1.000 | 32155 | tags=92%, list=59%, signal=223% | |
214 | CELLULAR RESPONSE TO BACTERIAL LIPOPROTEIN | 14 | -0.22 | -0.89 | 0.622 | 0.850 | 1.000 | 34735 | tags=93%, list=64%, signal=255% | |
215 | OPSONIZATION | 11 | -0.26 | -0.89 | 0.688 | 0.849 | 1.000 | 40630 | tags=100%, list=74%, signal=391% | |
216 | POSITIVE REGULATION OF STEROID BIOSYNTHETIC PROCESS | 17 | -0.21 | -0.89 | 0.750 | 0.848 | 1.000 | 35720 | tags=94%, list=65%, signal=272% | |
217 | NEGATIVE REGULATION OF BONE MINERALIZATION | 17 | -0.21 | -0.89 | 0.625 | 0.845 | 1.000 | 43345 | tags=100%, list=79%, signal=485% | |
218 | POSITIVE REGULATION OF URINE VOLUME | 17 | -0.21 | -0.88 | 0.710 | 0.856 | 1.000 | 43218 | tags=100%, list=79%, signal=479% | |
219 | LYMPHOID PROGENITOR CELL DIFFERENTIATION | 13 | -0.23 | -0.88 | 0.688 | 0.854 | 1.000 | 35484 | tags=92%, list=65%, signal=263% | |
220 | REGULATION OF CELL-CELL ADHESION INVOLVED IN GASTRULATION | 17 | -0.20 | -0.88 | 0.632 | 0.854 | 1.000 | 43421 | tags=100%, list=80%, signal=488% | |
221 | POSITIVE REGULATION OF NITRIC-OXIDE SYNTHASE BIOSYNTHETIC PROCESS | 16 | -0.21 | -0.87 | 0.722 | 0.857 | 1.000 | 33425 | tags=94%, list=61%, signal=242% | |
222 | NORADRENERGIC NEURON DIFFERENTIATION | 15 | -0.22 | -0.87 | 0.732 | 0.860 | 1.000 | 35160 | tags=93%, list=64%, signal=262% | |
223 | POSITIVE REGULATION OF TUMOR NECROSIS FACTOR BIOSYNTHETIC PROCESS | 22 | -0.19 | -0.87 | 0.800 | 0.859 | 1.000 | 38528 | tags=95%, list=71%, signal=324% | |
224 | REGULATION OF PROSTAGLANDIN SECRETION | 8 | -0.27 | -0.86 | 0.716 | 0.874 | 1.000 | 39738 | tags=100%, list=73%, signal=367% | |
225 | TOOTH MINERALIZATION | 17 | -0.21 | -0.86 | 0.789 | 0.874 | 1.000 | 43272 | tags=100%, list=79%, signal=481% | |
226 | REGULATION OF URINE VOLUME | 18 | -0.21 | -0.86 | 0.750 | 0.873 | 1.000 | 43218 | tags=100%, list=79%, signal=479% | |
227 | RESPONSE TO BACTERIAL LIPOPEPTIDE | 14 | -0.22 | -0.86 | 0.674 | 0.871 | 1.000 | 34735 | tags=93%, list=64%, signal=255% | |
228 | NEGATIVE REGULATION OF HUMORAL IMMUNE RESPONSE MEDIATED BY CIRCULATING IMMUNOGLOBULIN | 12 | -0.24 | -0.86 | 0.596 | 0.871 | 1.000 | 41516 | tags=100%, list=76%, signal=417% | |
229 | REGULATION OF HUMORAL IMMUNE RESPONSE MEDIATED BY CIRCULATING IMMUNOGLOBULIN | 12 | -0.24 | -0.86 | 0.649 | 0.868 | 1.000 | 41516 | tags=100%, list=76%, signal=417% | |
230 | POSITIVE REGULATION OF MALE GONAD DEVELOPMENT | 9 | -0.27 | -0.85 | 0.691 | 0.871 | 1.000 | 39807 | tags=100%, list=73%, signal=369% | |
231 | POSITIVE REGULATION OF KERATINOCYTE PROLIFERATION | 14 | -0.22 | -0.85 | 0.735 | 0.878 | 1.000 | 18634 | tags=79%, list=34%, signal=119% | |
232 | REGULATION OF CARDIAC MUSCLE CELL APOPTOTIC PROCESS | 17 | -0.20 | -0.85 | 0.700 | 0.876 | 1.000 | 43654 | tags=100%, list=80%, signal=498% | |
233 | NEGATIVE REGULATION OF HETEROTYPIC CELL-CELL ADHESION | 17 | -0.20 | -0.84 | 0.724 | 0.878 | 1.000 | 43421 | tags=100%, list=80%, signal=488% | |
234 | OLIGOPEPTIDE TRANSPORT | 5 | -0.34 | -0.84 | 0.671 | 0.876 | 1.000 | 35908 | tags=100%, list=66%, signal=292% | |
235 | NEGATIVE REGULATION OF PLATELET-DERIVED GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 24 | -0.18 | -0.84 | 0.700 | 0.873 | 1.000 | 40281 | tags=96%, list=74%, signal=365% | |
236 | REGULATION OF PROTEIN KINASE A SIGNALING | 15 | -0.22 | -0.84 | 0.730 | 0.877 | 1.000 | 34795 | tags=93%, list=64%, signal=257% | |
237 | SODIUM ION EXPORT | 26 | -0.17 | -0.84 | 1.000 | 0.875 | 1.000 | 45215 | tags=100%, list=83%, signal=581% | |
238 | CELLULAR RESPONSE TO BACTERIAL LIPOPEPTIDE | 14 | -0.22 | -0.83 | 0.707 | 0.882 | 1.000 | 34735 | tags=93%, list=64%, signal=255% | |
239 | RESPONSE TO MUSCLE STRETCH | 29 | -0.17 | -0.83 | 0.750 | 0.878 | 1.000 | 40831 | tags=97%, list=75%, signal=382% | |
240 | REGULATION OF INTERLEUKIN-6 BIOSYNTHETIC PROCESS | 18 | -0.20 | -0.83 | 0.846 | 0.878 | 1.000 | 36188 | tags=94%, list=66%, signal=280% | |
241 | BONE GROWTH | 22 | -0.18 | -0.83 | 0.800 | 0.878 | 1.000 | 44708 | tags=100%, list=82%, signal=551% | |
242 | LIPOPROTEIN LOCALIZATION | 17 | -0.19 | -0.83 | 0.813 | 0.878 | 1.000 | 36891 | tags=94%, list=68%, signal=290% | |
243 | PURINERGIC RECEPTOR SIGNALING PATHWAY | 10 | -0.23 | -0.82 | 0.848 | 0.892 | 1.000 | 41961 | tags=100%, list=77%, signal=432% | |
244 | NEGATIVE REGULATION OF STRIATED MUSCLE CONTRACTION | 14 | -0.21 | -0.81 | 0.824 | 0.892 | 1.000 | 25147 | tags=86%, list=46%, signal=159% | |
245 | NEGATIVE REGULATION OF CELL ADHESION MEDIATED BY INTEGRIN | 12 | -0.22 | -0.81 | 0.714 | 0.890 | 1.000 | 42872 | tags=100%, list=79%, signal=465% | |
246 | FAT-SOLUBLE VITAMIN CATABOLIC PROCESS | 7 | -0.28 | -0.81 | 0.704 | 0.888 | 1.000 | 39513 | tags=100%, list=72%, signal=362% | |
247 | GLUCOCORTICOID BIOSYNTHETIC PROCESS | 13 | -0.21 | -0.81 | 0.800 | 0.887 | 1.000 | 23899 | tags=85%, list=44%, signal=150% | |
248 | GLANDULAR EPITHELIAL CELL DIFFERENTIATION | 38 | -0.18 | -0.80 | 1.000 | 0.897 | 1.000 | 44546 | tags=100%, list=82%, signal=542% | |
249 | TRIGLYCERIDE-RICH LIPOPROTEIN PARTICLE REMODELING | 16 | -0.20 | -0.80 | 0.914 | 0.893 | 1.000 | 43677 | tags=100%, list=80%, signal=499% | |
250 | CELLULAR RESPONSE TO CGMP | 14 | -0.20 | -0.80 | 0.830 | 0.896 | 1.000 | 24879 | tags=86%, list=46%, signal=157% | |
251 | LIPOPROTEIN TRANSPORT | 17 | -0.19 | -0.80 | 0.880 | 0.897 | 1.000 | 36891 | tags=94%, list=68%, signal=290% | |
252 | INDOLE-CONTAINING COMPOUND METABOLIC PROCESS | 31 | -0.17 | -0.79 | 1.000 | 0.910 | 1.000 | 37411 | tags=94%, list=69%, signal=297% | |
253 | RESPONSE TO CGMP | 14 | -0.20 | -0.78 | 0.829 | 0.910 | 1.000 | 24879 | tags=86%, list=46%, signal=157% | |
254 | REGULATION OF GLUCOCORTICOID BIOSYNTHETIC PROCESS | 14 | -0.20 | -0.78 | 0.730 | 0.910 | 1.000 | 43870 | tags=100%, list=80%, signal=508% | |
255 | NEGATIVE REGULATION OF HORMONE BIOSYNTHETIC PROCESS | 14 | -0.20 | -0.78 | 0.833 | 0.910 | 1.000 | 43870 | tags=100%, list=80%, signal=508% | |
256 | SPINAL CORD MOTOR NEURON DIFFERENTIATION | 13 | -0.20 | -0.78 | 0.878 | 0.911 | 1.000 | 35160 | tags=92%, list=64%, signal=259% | |
257 | REGULATION OF CORTISOL BIOSYNTHETIC PROCESS | 14 | -0.20 | -0.78 | 0.824 | 0.907 | 1.000 | 43870 | tags=100%, list=80%, signal=508% | |
258 | HYALURONAN BIOSYNTHETIC PROCESS | 10 | -0.22 | -0.78 | 0.841 | 0.904 | 1.000 | 42535 | tags=100%, list=78%, signal=452% | |
259 | POSITIVE REGULATION OF APOPTOTIC CELL CLEARANCE | 8 | -0.26 | -0.78 | 0.757 | 0.900 | 1.000 | 40630 | tags=100%, list=74%, signal=391% | |
260 | MATING | 13 | -0.19 | -0.78 | 0.857 | 0.898 | 1.000 | 44044 | tags=100%, list=81%, signal=517% | |
261 | NEGATIVE REGULATION OF CREB TRANSCRIPTION FACTOR ACTIVITY | 8 | -0.26 | -0.78 | 0.819 | 0.895 | 1.000 | 25600 | tags=88%, list=47%, signal=165% | |
262 | TYPE B PANCREATIC CELL DEVELOPMENT | 16 | -0.19 | -0.77 | 0.875 | 0.900 | 1.000 | 44148 | tags=100%, list=81%, signal=522% | |
263 | NEUROTRANSMITTER UPTAKE | 18 | -0.17 | -0.76 | 0.900 | 0.907 | 1.000 | 45248 | tags=100%, list=83%, signal=583% | |
264 | ADENYLATE CYCLASE-INHIBITING G-PROTEIN COUPLED GLUTAMATE RECEPTOR SIGNALING PATHWAY | 8 | -0.25 | -0.76 | 0.869 | 0.909 | 1.000 | 25865 | tags=88%, list=47%, signal=166% | |
265 | GLANDULAR EPITHELIAL CELL DEVELOPMENT | 18 | -0.18 | -0.75 | 0.960 | 0.918 | 1.000 | 44546 | tags=100%, list=82%, signal=542% | |
266 | AORTIC VALVE DEVELOPMENT | 8 | -0.24 | -0.74 | 0.844 | 0.925 | 1.000 | 41544 | tags=100%, list=76%, signal=418% | |
267 | AORTIC VALVE MORPHOGENESIS | 8 | -0.24 | -0.74 | 0.863 | 0.923 | 1.000 | 41544 | tags=100%, list=76%, signal=418% | |
268 | CEREBELLAR CORTEX FORMATION | 20 | -0.16 | -0.74 | 0.833 | 0.920 | 1.000 | 28847 | tags=85%, list=53%, signal=180% | |
269 | RENAL SYSTEM VASCULATURE MORPHOGENESIS | 9 | -0.23 | -0.74 | 0.880 | 0.917 | 1.000 | 42057 | tags=100%, list=77%, signal=435% | |
270 | BUNDLE OF HIS CELL ACTION POTENTIAL | 3 | -0.37 | -0.73 | 0.847 | 0.921 | 1.000 | 34431 | tags=100%, list=63%, signal=271% | |
271 | BUNDLE OF HIS CELL TO PURKINJE MYOCYTE SIGNALING | 3 | -0.37 | -0.73 | 0.802 | 0.919 | 1.000 | 34431 | tags=100%, list=63%, signal=271% | |
272 | NEGATIVE REGULATION OF AMINE TRANSPORT | 11 | -0.20 | -0.73 | 0.847 | 0.918 | 1.000 | 43626 | tags=100%, list=80%, signal=497% | |
273 | KIDNEY VASCULATURE MORPHOGENESIS | 9 | -0.23 | -0.73 | 0.848 | 0.922 | 1.000 | 42057 | tags=100%, list=77%, signal=435% | |
274 | CELL DIFFERENTIATION IN HINDBRAIN | 20 | -0.15 | -0.71 | 1.000 | 0.933 | 1.000 | 28847 | tags=85%, list=53%, signal=180% | |
275 | CORONARY VASCULATURE DEVELOPMENT | 21 | -0.17 | -0.69 | 0.955 | 0.948 | 1.000 | 45529 | tags=100%, list=83%, signal=601% | |
276 | IMMATURE B CELL DIFFERENTIATION | 18 | -0.15 | -0.68 | 0.964 | 0.951 | 1.000 | 46285 | tags=100%, list=85%, signal=656% | |
277 | NEGATIVE REGULATION OF FIBRINOLYSIS | 21 | -0.16 | -0.68 | 0.917 | 0.950 | 1.000 | 30102 | tags=86%, list=55%, signal=191% | |
278 | CELLULAR SODIUM ION HOMEOSTASIS | 27 | -0.17 | -0.68 | 1.000 | 0.946 | 1.000 | 45215 | tags=100%, list=83%, signal=581% | |
279 | SMOOTH MUSCLE TISSUE DEVELOPMENT | 23 | -0.14 | -0.68 | 1.000 | 0.948 | 1.000 | 42057 | tags=96%, list=77%, signal=416% | |
280 | NEGATIVE REGULATION OF VASCULAR PERMEABILITY | 16 | -0.16 | -0.67 | 1.000 | 0.950 | 1.000 | 38362 | tags=94%, list=70%, signal=315% | |
281 | RESPONSE TO BACTERIAL LIPOPROTEIN | 15 | -0.18 | -0.66 | 0.964 | 0.950 | 1.000 | 37744 | tags=93%, list=69%, signal=302% | |
282 | PHAGOCYTOSIS, RECOGNITION | 17 | -0.17 | -0.66 | 1.000 | 0.947 | 1.000 | 37505 | tags=94%, list=69%, signal=300% | |
283 | POSITIVE REGULATION OF INOSITOL PHOSPHATE BIOSYNTHETIC PROCESS | 11 | -0.19 | -0.66 | 0.962 | 0.945 | 1.000 | 34577 | tags=91%, list=63%, signal=248% | |
284 | NEGATIVE REGULATION OF INTERLEUKIN-1 PRODUCTION | 17 | -0.16 | -0.66 | 1.000 | 0.946 | 1.000 | 38742 | tags=94%, list=71%, signal=324% | |
285 | REGULATION OF T-HELPER 17 TYPE IMMUNE RESPONSE | 13 | -0.19 | -0.65 | 0.963 | 0.943 | 1.000 | 27526 | tags=85%, list=50%, signal=171% | |
286 | SUPEROXIDE ANION GENERATION | 17 | -0.17 | -0.65 | 0.931 | 0.945 | 1.000 | 32452 | tags=88%, list=59%, signal=217% | |
287 | REGULATION OF INOSITOL PHOSPHATE BIOSYNTHETIC PROCESS | 13 | -0.17 | -0.63 | 1.000 | 0.949 | 1.000 | 37520 | tags=92%, list=69%, signal=295% | |
288 | RESPONSE TO MERCURY ION | 8 | -0.20 | -0.62 | 0.990 | 0.952 | 1.000 | 43604 | tags=100%, list=80%, signal=496% | |
289 | HEART FORMATION | 11 | -0.18 | -0.61 | 0.941 | 0.952 | 1.000 | 28197 | tags=82%, list=52%, signal=169% | |
290 | POSITIVE REGULATION OF INTERFERON-GAMMA SECRETION | 9 | -0.18 | -0.61 | 0.988 | 0.948 | 1.000 | 33615 | tags=89%, list=62%, signal=231% | |
291 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL MIGRATION | 36 | -0.13 | -0.59 | 1.000 | 0.952 | 1.000 | 32482 | tags=86%, list=59%, signal=212% | |
292 | POSITIVE REGULATION OF CELL FATE COMMITMENT | 13 | -0.16 | -0.58 | 1.000 | 0.951 | 1.000 | 46119 | tags=100%, list=84%, signal=643% | |
293 | TOLERANCE INDUCTION | 12 | -0.14 | -0.56 | 1.000 | 0.953 | 1.000 | 46955 | tags=100%, list=86%, signal=713% | |
294 | GABAERGIC NEURON DIFFERENTIATION | 14 | -0.15 | -0.54 | 1.000 | 0.951 | 1.000 | 33304 | tags=86%, list=61%, signal=220% |