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 | REGULATION OF NATURAL KILLER CELL CHEMOTAXIS | Details ... | 12 | 0.66 | 1.41 | 0.106 | 1.000 | 0.963 | 18582 | tags=100%, list=34%, signal=151% |
2 | RESPONSE TO CORTICOTROPIN-RELEASING HORMONE | Details ... | 12 | 0.56 | 1.35 | 0.160 | 1.000 | 0.980 | 24083 | tags=100%, list=44%, signal=179% |
3 | CELLULAR RESPONSE TO CORTICOTROPIN-RELEASING HORMONE STIMULUS | Details ... | 12 | 0.56 | 1.35 | 0.160 | 1.000 | 0.980 | 24083 | tags=100%, list=44%, signal=179% |
4 | POSITIVE REGULATION OF NATURAL KILLER CELL CHEMOTAXIS | Details ... | 9 | 0.66 | 1.33 | 0.156 | 1.000 | 0.981 | 18582 | tags=100%, list=34%, signal=151% |
5 | AMACRINE CELL DIFFERENTIATION | Details ... | 8 | 0.55 | 1.27 | 0.170 | 1.000 | 0.992 | 24422 | tags=100%, list=45%, signal=181% |
6 | REGULATION OF RENAL SODIUM EXCRETION | Details ... | 9 | 0.58 | 1.22 | 0.270 | 1.000 | 0.997 | 22841 | tags=100%, list=42%, signal=172% |
7 | REGULATION OF GUANYLATE CYCLASE ACTIVITY | Details ... | 12 | 0.49 | 1.19 | 0.265 | 1.000 | 0.998 | 27854 | tags=100%, list=51%, signal=204% |
8 | POSITIVE REGULATION OF GUANYLATE CYCLASE ACTIVITY | Details ... | 10 | 0.49 | 1.16 | 0.308 | 1.000 | 1.000 | 27854 | tags=100%, list=51%, signal=204% |
9 | MINERALOCORTICOID BIOSYNTHETIC PROCESS | Details ... | 9 | 0.46 | 1.14 | 0.278 | 1.000 | 1.000 | 15121 | tags=89%, list=28%, signal=123% |
10 | MINERALOCORTICOID METABOLIC PROCESS | Details ... | 9 | 0.46 | 1.14 | 0.278 | 1.000 | 1.000 | 15121 | tags=89%, list=28%, signal=123% |
11 | ADULT HEART DEVELOPMENT | Details ... | 10 | 0.51 | 1.10 | 0.362 | 1.000 | 1.000 | 26936 | tags=100%, list=49%, signal=197% |
12 | REGULATION OF CELLULAR GLUCURONIDATION | Details ... | 13 | 0.47 | 1.07 | 0.390 | 1.000 | 1.000 | 29208 | tags=100%, list=53%, signal=215% |
13 | INDOLE-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | Details ... | 9 | 0.42 | 1.06 | 0.387 | 1.000 | 1.000 | 31569 | tags=100%, list=58%, signal=237% |
14 | INDOLALKYLAMINE BIOSYNTHETIC PROCESS | Details ... | 9 | 0.42 | 1.06 | 0.387 | 1.000 | 1.000 | 31569 | tags=100%, list=58%, signal=237% |
15 | POSITIVE REGULATION OF INSULIN-LIKE GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | Details ... | 23 | 0.36 | 1.03 | 0.447 | 1.000 | 1.000 | 30347 | tags=96%, list=56%, signal=215% |
16 | BEHAVIORAL RESPONSE TO NICOTINE | Details ... | 11 | 0.47 | 1.03 | 0.435 | 1.000 | 1.000 | 13770 | tags=82%, list=25%, signal=109% |
17 | REGULATION OF CHEMOKINE-MEDIATED SIGNALING PATHWAY | Details ... | 14 | 0.40 | 1.02 | 0.456 | 1.000 | 1.000 | 19085 | tags=86%, list=35%, signal=132% |
18 | NEGATIVE REGULATION OF CELL VOLUME | Details ... | 13 | 0.37 | 1.02 | 0.451 | 1.000 | 1.000 | 34395 | tags=100%, list=63%, signal=270% |
19 | NEGATIVE REGULATION OF CYTOKINE SECRETION INVOLVED IN IMMUNE RESPONSE | Details ... | 8 | 0.55 | 1.01 | 0.494 | 1.000 | 1.000 | 24499 | tags=100%, list=45%, signal=181% |
20 | REGULATION OF PROTEIN KINASE A SIGNALING | Details ... | 15 | 0.36 | 1.00 | 0.461 | 1.000 | 1.000 | 34790 | tags=100%, list=64%, signal=275% |
21 | RENAL SYSTEM VASCULATURE MORPHOGENESIS | 9 | 0.42 | 1.00 | 0.482 | 1.000 | 1.000 | 31748 | tags=100%, list=58%, signal=238% | |
22 | KIDNEY VASCULATURE MORPHOGENESIS | 9 | 0.42 | 1.00 | 0.482 | 1.000 | 1.000 | 31748 | tags=100%, list=58%, signal=238% | |
23 | REGULATION OF SKELETAL MUSCLE CONTRACTION | 14 | 0.35 | 0.99 | 0.461 | 1.000 | 1.000 | 35740 | tags=100%, list=65%, signal=289% | |
24 | REGULATION OF SEQUESTERING OF ZINC ION | 11 | 0.38 | 0.99 | 0.440 | 1.000 | 1.000 | 7990 | tags=64%, list=15%, signal=75% | |
25 | INTERMEDIATE FILAMENT BUNDLE ASSEMBLY | 12 | 0.38 | 0.99 | 0.472 | 1.000 | 1.000 | 34094 | tags=100%, list=62%, signal=266% | |
26 | REGULATION OF VASODILATION | 23 | 0.30 | 0.97 | 0.525 | 1.000 | 1.000 | 28896 | tags=91%, list=53%, signal=194% | |
27 | IMMUNOLOGICAL SYNAPSE FORMATION | 12 | 0.40 | 0.96 | 0.512 | 1.000 | 1.000 | 32633 | tags=100%, list=60%, signal=248% | |
28 | REGULATION OF SOMITOGENESIS | 12 | 0.37 | 0.96 | 0.505 | 1.000 | 1.000 | 1965 | tags=50%, list=4%, signal=52% | |
29 | NEGATIVE REGULATION OF CHEMOKINE-MEDIATED SIGNALING PATHWAY | 13 | 0.38 | 0.96 | 0.517 | 1.000 | 1.000 | 19085 | tags=85%, list=35%, signal=130% | |
30 | EYE PHOTORECEPTOR CELL DEVELOPMENT | 18 | 0.34 | 0.96 | 0.508 | 1.000 | 1.000 | 30403 | tags=94%, list=56%, signal=213% | |
31 | FOREBRAIN REGIONALIZATION | 9 | 0.38 | 0.95 | 0.515 | 1.000 | 1.000 | 33912 | tags=100%, list=62%, signal=263% | |
32 | METANEPHRIC GLOMERULUS DEVELOPMENT | 14 | 0.40 | 0.95 | 0.542 | 1.000 | 1.000 | 32576 | tags=100%, list=60%, signal=247% | |
33 | METANEPHRIC GLOMERULUS VASCULATURE DEVELOPMENT | 13 | 0.40 | 0.94 | 0.518 | 1.000 | 1.000 | 32576 | tags=100%, list=60%, signal=247% | |
34 | SKELETAL MUSCLE THIN FILAMENT ASSEMBLY | 11 | 0.38 | 0.93 | 0.517 | 1.000 | 1.000 | 25153 | tags=91%, list=46%, signal=168% | |
35 | NEURONAL SIGNAL TRANSDUCTION | 15 | 0.36 | 0.93 | 0.542 | 1.000 | 1.000 | 26894 | tags=93%, list=49%, signal=184% | |
36 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT5 PROTEIN | 36 | 0.28 | 0.92 | 0.546 | 1.000 | 1.000 | 35965 | tags=97%, list=66%, signal=284% | |
37 | REGULATION OF EXCRETION | 12 | 0.39 | 0.92 | 0.538 | 1.000 | 1.000 | 22841 | tags=92%, list=42%, signal=157% | |
38 | POSITIVE REGULATION OF PROTEIN KINASE A SIGNALING | 10 | 0.36 | 0.91 | 0.584 | 1.000 | 1.000 | 34790 | tags=100%, list=64%, signal=275% | |
39 | POSITIVE REGULATION OF KERATINOCYTE PROLIFERATION | 14 | 0.32 | 0.91 | 0.579 | 1.000 | 1.000 | 23153 | tags=86%, list=42%, signal=149% | |
40 | SUBPALLIUM DEVELOPMENT | 23 | 0.29 | 0.91 | 0.574 | 1.000 | 1.000 | 34507 | tags=96%, list=63%, signal=259% | |
41 | STRIATUM DEVELOPMENT | 23 | 0.29 | 0.91 | 0.574 | 1.000 | 1.000 | 34507 | tags=96%, list=63%, signal=259% | |
42 | NEGATIVE REGULATION OF T-HELPER CELL DIFFERENTIATION | 16 | 0.30 | 0.90 | 0.598 | 1.000 | 1.000 | 38348 | tags=100%, list=70%, signal=335% | |
43 | GANGLIOSIDE BIOSYNTHETIC PROCESS | 11 | 0.34 | 0.90 | 0.568 | 1.000 | 1.000 | 36014 | tags=100%, list=66%, signal=293% | |
44 | GLOMERULUS MORPHOGENESIS | 15 | 0.33 | 0.90 | 0.615 | 1.000 | 1.000 | 36865 | tags=100%, list=67%, signal=307% | |
45 | OLFACTORY BULB INTERNEURON DIFFERENTIATION | 15 | 0.32 | 0.89 | 0.598 | 1.000 | 1.000 | 37365 | tags=100%, list=68%, signal=316% | |
46 | POSITIVE REGULATION OF VASODILATION | 19 | 0.27 | 0.87 | 0.682 | 1.000 | 1.000 | 28896 | tags=89%, list=53%, signal=190% | |
47 | REGULATION OF GLUCURONOSYLTRANSFERASE ACTIVITY | 9 | 0.47 | 0.87 | 0.603 | 1.000 | 1.000 | 29208 | tags=100%, list=53%, signal=215% | |
48 | NEGATIVE REGULATION OF GLUCURONOSYLTRANSFERASE ACTIVITY | 9 | 0.47 | 0.87 | 0.603 | 1.000 | 1.000 | 29208 | tags=100%, list=53%, signal=215% | |
49 | NEGATIVE REGULATION OF CELLULAR GLUCURONIDATION | 9 | 0.47 | 0.87 | 0.603 | 1.000 | 1.000 | 29208 | tags=100%, list=53%, signal=215% | |
50 | RESPONSE TO POTASSIUM ION | 8 | 0.35 | 0.87 | 0.637 | 1.000 | 1.000 | 35283 | tags=100%, list=65%, signal=282% | |
51 | CELLULAR RESPONSE TO POTASSIUM ION | 8 | 0.35 | 0.87 | 0.637 | 1.000 | 1.000 | 35283 | tags=100%, list=65%, signal=282% | |
52 | PLASMINOGEN ACTIVATION | 14 | 0.35 | 0.86 | 0.581 | 1.000 | 1.000 | 35387 | tags=100%, list=65%, signal=283% | |
53 | FLAVONOID GLUCURONIDATION | 8 | 0.47 | 0.85 | 0.626 | 1.000 | 1.000 | 29208 | tags=100%, list=53%, signal=215% | |
54 | XENOBIOTIC GLUCURONIDATION | 8 | 0.47 | 0.85 | 0.626 | 1.000 | 1.000 | 29208 | tags=100%, list=53%, signal=215% | |
55 | TRANSCRIPTION, RNA-TEMPLATED | 2 | 0.56 | 0.84 | 0.708 | 1.000 | 1.000 | 23986 | tags=100%, list=44%, signal=178% | |
56 | ATRIAL CARDIAC MUSCLE CELL ACTION POTENTIAL | 14 | 0.29 | 0.84 | 0.667 | 1.000 | 1.000 | 38773 | tags=100%, list=71%, signal=344% | |
57 | ATRIAL CARDIAC MUSCLE CELL TO AV NODE CELL SIGNALING | 14 | 0.29 | 0.84 | 0.667 | 1.000 | 1.000 | 38773 | tags=100%, list=71%, signal=344% | |
58 | ATRIAL CARDIAC MUSCLE CELL TO AV NODE CELL COMMUNICATION | 14 | 0.29 | 0.84 | 0.667 | 1.000 | 1.000 | 38773 | tags=100%, list=71%, signal=344% | |
59 | REGULATION OF SYNAPSE STRUCTURAL PLASTICITY | 12 | 0.33 | 0.83 | 0.677 | 1.000 | 1.000 | 28702 | tags=92%, list=52%, signal=193% | |
60 | MYOBLAST FUSION | 14 | 0.28 | 0.83 | 0.745 | 1.000 | 1.000 | 73 | tags=14%, list=0%, signal=14% | |
61 | NEGATIVE REGULATION OF LYMPHOCYTE MIGRATION | 12 | 0.31 | 0.83 | 0.701 | 1.000 | 1.000 | 37746 | tags=100%, list=69%, signal=323% | |
62 | PHENOL-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 34 | 0.23 | 0.83 | 0.706 | 1.000 | 1.000 | 26927 | tags=85%, list=49%, signal=168% | |
63 | REGULATION OF STEROID HORMONE SECRETION | 16 | 0.28 | 0.82 | 0.744 | 1.000 | 1.000 | 39351 | tags=100%, list=72%, signal=357% | |
64 | POSITIVE REGULATION OF CELL FATE COMMITMENT | 13 | 0.30 | 0.82 | 0.716 | 1.000 | 1.000 | 38062 | tags=100%, list=70%, signal=329% | |
65 | IRIS MORPHOGENESIS | 7 | 0.35 | 0.81 | 0.721 | 1.000 | 1.000 | 35539 | tags=100%, list=65%, signal=286% | |
66 | GANGLIOSIDE METABOLIC PROCESS | 22 | 0.25 | 0.81 | 0.732 | 1.000 | 1.000 | 36015 | tags=95%, list=66%, signal=280% | |
67 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL MIGRATION | 36 | 0.26 | 0.81 | 0.706 | 1.000 | 1.000 | 37300 | tags=97%, list=68%, signal=306% | |
68 | ADENYLATE CYCLASE-INHIBITING G-PROTEIN COUPLED GLUTAMATE RECEPTOR SIGNALING PATHWAY | 8 | 0.33 | 0.81 | 0.712 | 1.000 | 1.000 | 36491 | tags=100%, list=67%, signal=301% | |
69 | PURKINJE MYOCYTE TO VENTRICULAR CARDIAC MUSCLE CELL SIGNALING | 4 | 0.45 | 0.81 | 0.739 | 1.000 | 1.000 | 30309 | tags=100%, list=55%, signal=224% | |
70 | PURKINJE MYOCYTE TO VENTRICULAR CARDIAC MUSCLE CELL COMMUNICATION | 4 | 0.45 | 0.81 | 0.739 | 1.000 | 1.000 | 30309 | tags=100%, list=55%, signal=224% | |
71 | GLYCOSPHINGOLIPID BIOSYNTHETIC PROCESS | 24 | 0.26 | 0.81 | 0.731 | 1.000 | 1.000 | 36014 | tags=96%, list=66%, signal=281% | |
72 | NEGATIVE REGULATION OF CELLULAR EXTRAVASATION | 12 | 0.29 | 0.80 | 0.719 | 1.000 | 1.000 | 38744 | tags=100%, list=71%, signal=343% | |
73 | CANNABINOID SIGNALING PATHWAY | 7 | 0.37 | 0.80 | 0.737 | 1.000 | 1.000 | 16993 | tags=86%, list=31%, signal=124% | |
74 | HINDLIMB MORPHOGENESIS | 14 | 0.30 | 0.80 | 0.699 | 1.000 | 1.000 | 38215 | tags=100%, list=70%, signal=332% | |
75 | POSITIVE REGULATION OF MULTICELLULAR ORGANISM GROWTH | 21 | 0.33 | 0.80 | 0.723 | 1.000 | 1.000 | 11123 | tags=81%, list=20%, signal=102% | |
76 | REGULATION OF ATRIAL CARDIAC MUSCLE CELL MEMBRANE DEPOLARIZATION | 10 | 0.34 | 0.80 | 0.699 | 1.000 | 1.000 | 35890 | tags=100%, list=66%, signal=291% | |
77 | REGULATION OF MYOBLAST PROLIFERATION | 5 | 0.39 | 0.79 | 0.729 | 1.000 | 1.000 | 33240 | tags=100%, list=61%, signal=255% | |
78 | SEROTONIN RECEPTOR SIGNALING PATHWAY | 23 | 0.29 | 0.79 | 0.732 | 1.000 | 1.000 | 25708 | tags=87%, list=47%, signal=164% | |
79 | REGULATION OF ACTIVATION OF JAK2 KINASE ACTIVITY | 20 | 0.33 | 0.79 | 0.691 | 1.000 | 1.000 | 16984 | tags=85%, list=31%, signal=123% | |
80 | CORNEA DEVELOPMENT IN CAMERA-TYPE EYE | 13 | 0.29 | 0.79 | 0.736 | 1.000 | 1.000 | 27468 | tags=92%, list=50%, signal=185% | |
81 | REGULATION OF GLUCOCORTICOID SECRETION | 10 | 0.30 | 0.79 | 0.740 | 1.000 | 1.000 | 15168 | tags=80%, list=28%, signal=111% | |
82 | REGULATION OF PHOSPHATIDYLINOSITOL BIOSYNTHETIC PROCESS | 13 | 0.27 | 0.79 | 0.777 | 1.000 | 1.000 | 32576 | tags=92%, list=60%, signal=228% | |
83 | COMPLEMENT ACTIVATION, CLASSICAL PATHWAY | 70 | 0.28 | 0.78 | 0.654 | 1.000 | 1.000 | 21683 | tags=84%, list=40%, signal=140% | |
84 | COMPLEMENT ACTIVATION, LECTIN PATHWAY | 15 | 0.31 | 0.78 | 0.720 | 1.000 | 1.000 | 37726 | tags=100%, list=69%, signal=322% | |
85 | DETECTION OF MECHANICAL STIMULUS INVOLVED IN SENSORY PERCEPTION | 16 | 0.27 | 0.78 | 0.758 | 1.000 | 1.000 | 39971 | tags=100%, list=73%, signal=372% | |
86 | ENTEROENDOCRINE CELL DIFFERENTIATION | 25 | 0.23 | 0.78 | 0.773 | 1.000 | 1.000 | 41977 | tags=100%, list=77%, signal=430% | |
87 | TERPENOID CATABOLIC PROCESS | 5 | 0.40 | 0.78 | 0.724 | 1.000 | 1.000 | 32816 | tags=100%, list=60%, signal=250% | |
88 | EMBRYONIC HINDLIMB MORPHOGENESIS | 11 | 0.30 | 0.78 | 0.730 | 1.000 | 1.000 | 38215 | tags=100%, list=70%, signal=332% | |
89 | POSITIVE REGULATION OF MEMORY T CELL DIFFERENTIATION | 11 | 0.30 | 0.78 | 0.736 | 1.000 | 1.000 | 38062 | tags=100%, list=70%, signal=329% | |
90 | MALE GENITALIA DEVELOPMENT | 13 | 0.32 | 0.77 | 0.745 | 1.000 | 1.000 | 29004 | tags=92%, list=53%, signal=197% | |
91 | REGULATION OF CORTICOSTEROID HORMONE SECRETION | 12 | 0.28 | 0.76 | 0.767 | 1.000 | 1.000 | 39351 | tags=100%, list=72%, signal=357% | |
92 | EOSINOPHIL CHEMOTAXIS | 12 | 0.32 | 0.75 | 0.764 | 1.000 | 1.000 | 16984 | tags=83%, list=31%, signal=121% | |
93 | EOSINOPHIL MIGRATION | 12 | 0.32 | 0.75 | 0.764 | 1.000 | 1.000 | 16984 | tags=83%, list=31%, signal=121% | |
94 | ATRIOVENTRICULAR CANAL DEVELOPMENT | 18 | 0.24 | 0.75 | 0.798 | 1.000 | 1.000 | 34447 | tags=94%, list=63%, signal=255% | |
95 | OPSONIZATION | 11 | 0.30 | 0.75 | 0.803 | 1.000 | 1.000 | 38194 | tags=100%, list=70%, signal=332% | |
96 | ACTIVATION OF PROTEIN KINASE B ACTIVITY | 47 | 0.20 | 0.75 | 0.832 | 1.000 | 1.000 | 34980 | tags=91%, list=64%, signal=254% | |
97 | EQUILIBRIOCEPTION | 17 | 0.28 | 0.75 | 0.752 | 1.000 | 1.000 | 31659 | tags=94%, list=58%, signal=224% | |
98 | TYPE B PANCREATIC CELL DIFFERENTIATION | 21 | 0.23 | 0.75 | 0.821 | 1.000 | 1.000 | 41977 | tags=100%, list=77%, signal=430% | |
99 | REGULATION OF ADENYLATE CYCLASE ACTIVITY INVOLVED IN G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 7 | 0.35 | 0.74 | 0.800 | 1.000 | 1.000 | 35308 | tags=100%, list=65%, signal=282% | |
100 | POSITIVE REGULATION OF ADENYLATE CYCLASE ACTIVITY INVOLVED IN G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 7 | 0.35 | 0.74 | 0.800 | 1.000 | 1.000 | 35308 | tags=100%, list=65%, signal=282% | |
101 | REGULATION OF CGMP BIOSYNTHETIC PROCESS | 16 | 0.28 | 0.74 | 0.787 | 1.000 | 1.000 | 21509 | tags=81%, list=39%, signal=134% | |
102 | CALCIUM-INDEPENDENT CELL-CELL ADHESION VIA PLASMA MEMBRANE CELL-ADHESION MOLECULES | 37 | 0.21 | 0.73 | 0.816 | 1.000 | 1.000 | 43087 | tags=100%, list=79%, signal=472% | |
103 | GLOMERULAR MESANGIUM DEVELOPMENT | 12 | 0.30 | 0.73 | 0.787 | 1.000 | 1.000 | 18499 | tags=75%, list=34%, signal=113% | |
104 | INTRACILIARY TRANSPORT INVOLVED IN CILIUM MORPHOGENESIS | 16 | 0.32 | 0.73 | 0.712 | 1.000 | 1.000 | 32066 | tags=94%, list=59%, signal=227% | |
105 | REGULATION OF POSTSYNAPTIC MEMBRANE POTENTIAL | 28 | 0.25 | 0.73 | 0.801 | 1.000 | 1.000 | 1122 | tags=25%, list=2%, signal=26% | |
106 | LACTATION | 13 | 0.28 | 0.73 | 0.827 | 1.000 | 1.000 | 39271 | tags=100%, list=72%, signal=355% | |
107 | GAS TRANSPORT | 18 | 0.34 | 0.73 | 0.733 | 1.000 | 1.000 | 24686 | tags=89%, list=45%, signal=162% | |
108 | CELLULAR GLUCURONIDATION | 24 | 0.25 | 0.73 | 0.779 | 1.000 | 1.000 | 29355 | tags=88%, list=54%, signal=189% | |
109 | SYNCYTIUM FORMATION | 22 | 0.21 | 0.72 | 0.896 | 1.000 | 1.000 | 1048 | tags=18%, list=2%, signal=19% | |
110 | POSITIVE REGULATION OF STEROID HORMONE SECRETION | 12 | 0.28 | 0.72 | 0.819 | 1.000 | 1.000 | 39351 | tags=100%, list=72%, signal=357% | |
111 | RENAL SYSTEM VASCULATURE DEVELOPMENT | 33 | 0.24 | 0.72 | 0.775 | 1.000 | 1.000 | 32576 | tags=91%, list=60%, signal=225% | |
112 | KIDNEY VASCULATURE DEVELOPMENT | 33 | 0.24 | 0.72 | 0.775 | 1.000 | 1.000 | 32576 | tags=91%, list=60%, signal=225% | |
113 | CARDIAC MUSCLE FIBER DEVELOPMENT | 23 | 0.23 | 0.72 | 0.806 | 1.000 | 1.000 | 27123 | tags=83%, list=50%, signal=164% | |
114 | POSITIVE REGULATION OF ACTIVATION OF JAK2 KINASE ACTIVITY | 17 | 0.32 | 0.72 | 0.771 | 1.000 | 1.000 | 1928 | tags=41%, list=4%, signal=43% | |
115 | SENSORY PERCEPTION OF TEMPERATURE STIMULUS | 10 | 0.29 | 0.71 | 0.811 | 1.000 | 1.000 | 39003 | tags=100%, list=71%, signal=349% | |
116 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT5 PROTEIN | 50 | 0.20 | 0.71 | 0.872 | 1.000 | 1.000 | 33397 | tags=90%, list=61%, signal=231% | |
117 | NEUROPEPTIDE SIGNALING PATHWAY | 50 | 0.20 | 0.71 | 0.861 | 1.000 | 1.000 | 21953 | tags=80%, list=40%, signal=134% | |
118 | RESPONSE TO HISTAMINE | 25 | 0.24 | 0.70 | 0.786 | 1.000 | 1.000 | 29900 | tags=88%, list=55%, signal=194% | |
119 | CELLULAR RESPONSE TO MAGNESIUM ION | 10 | 0.30 | 0.70 | 0.817 | 1.000 | 1.000 | 29320 | tags=90%, list=54%, signal=194% | |
120 | PARTURITION | 13 | 0.27 | 0.70 | 0.833 | 1.000 | 1.000 | 31202 | tags=92%, list=57%, signal=215% | |
121 | REGULATION OF T-HELPER 17 CELL DIFFERENTIATION | 10 | 0.30 | 0.70 | 0.812 | 1.000 | 1.000 | 38062 | tags=100%, list=70%, signal=329% | |
122 | RETINAL GANGLION CELL AXON GUIDANCE | 18 | 0.22 | 0.70 | 0.861 | 1.000 | 1.000 | 42604 | tags=100%, list=78%, signal=453% | |
123 | SKELETAL MUSCLE CELL DIFFERENTIATION | 9 | 0.26 | 0.70 | 0.874 | 1.000 | 1.000 | 548 | tags=22%, list=1%, signal=22% | |
124 | GLOMERULUS VASCULATURE DEVELOPMENT | 32 | 0.23 | 0.69 | 0.807 | 1.000 | 1.000 | 30038 | tags=88%, list=55%, signal=194% | |
125 | REGULATION OF GENERATION OF L-TYPE CALCIUM CURRENT | 14 | 0.22 | 0.69 | 0.903 | 1.000 | 1.000 | 73 | tags=14%, list=0%, signal=14% | |
126 | SMOOTH MUSCLE TISSUE DEVELOPMENT | 23 | 0.23 | 0.69 | 0.832 | 1.000 | 1.000 | 41948 | tags=100%, list=77%, signal=429% | |
127 | NEGATIVE REGULATION OF NEUROLOGICAL SYSTEM PROCESS | 9 | 0.27 | 0.69 | 0.873 | 1.000 | 1.000 | 39970 | tags=100%, list=73%, signal=372% | |
128 | REGULATION OF NLRP3 INFLAMMASOME COMPLEX ASSEMBLY | 17 | 0.31 | 0.69 | 0.783 | 1.000 | 1.000 | 33286 | tags=94%, list=61%, signal=241% | |
129 | POSITIVE REGULATION OF CORTICOSTEROID HORMONE SECRETION | 9 | 0.28 | 0.69 | 0.852 | 1.000 | 1.000 | 39351 | tags=100%, list=72%, signal=357% | |
130 | RESPONSE TO MAGNESIUM ION | 22 | 0.23 | 0.69 | 0.820 | 1.000 | 1.000 | 29320 | tags=86%, list=54%, signal=186% | |
131 | GLANDULAR EPITHELIAL CELL DEVELOPMENT | 18 | 0.23 | 0.68 | 0.852 | 1.000 | 1.000 | 41977 | tags=100%, list=77%, signal=430% | |
132 | NEGATIVE REGULATION OF LIPOPROTEIN LIPASE ACTIVITY | 12 | 0.26 | 0.68 | 0.828 | 1.000 | 1.000 | 40362 | tags=100%, list=74%, signal=382% | |
133 | HUMORAL IMMUNE RESPONSE MEDIATED BY CIRCULATING IMMUNOGLOBULIN | 84 | 0.23 | 0.68 | 0.758 | 1.000 | 1.000 | 34430 | tags=94%, list=63%, signal=254% | |
134 | POSITIVE REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 15 | 0.22 | 0.67 | 0.882 | 1.000 | 1.000 | 42432 | tags=100%, list=78%, signal=446% | |
135 | NEUROMUSCULAR SYNAPTIC TRANSMISSION | 22 | 0.22 | 0.67 | 0.860 | 1.000 | 1.000 | 19087 | tags=73%, list=35%, signal=112% | |
136 | TYPE B PANCREATIC CELL DEVELOPMENT | 16 | 0.23 | 0.67 | 0.844 | 1.000 | 1.000 | 41977 | tags=100%, list=77%, signal=430% | |
137 | REGULATION OF CELL COMMUNICATION BY ELECTRICAL COUPLING | 33 | 0.20 | 0.67 | 0.879 | 1.000 | 1.000 | 43511 | tags=100%, list=80%, signal=489% | |
138 | LEUKOCYTE MIGRATION INVOLVED IN INFLAMMATORY RESPONSE | 7 | 0.46 | 0.67 | 0.910 | 1.000 | 1.000 | 29626 | tags=100%, list=54%, signal=218% | |
139 | IMIDAZOLE-CONTAINING COMPOUND METABOLIC PROCESS | 20 | 0.23 | 0.66 | 0.852 | 1.000 | 1.000 | 36319 | tags=95%, list=66%, signal=283% | |
140 | NEGATIVE REGULATION OF HORMONE METABOLIC PROCESS | 15 | 0.24 | 0.66 | 0.856 | 1.000 | 1.000 | 34096 | tags=93%, list=62%, signal=248% | |
141 | DOPAMINERGIC NEURON DIFFERENTIATION | 31 | 0.20 | 0.66 | 0.846 | 1.000 | 1.000 | 43701 | tags=100%, list=80%, signal=498% | |
142 | CELLULAR RESPONSE TO HISTAMINE | 18 | 0.25 | 0.66 | 0.836 | 1.000 | 1.000 | 29900 | tags=89%, list=55%, signal=196% | |
143 | NEGATIVE REGULATION OF GASTRULATION | 11 | 0.22 | 0.66 | 0.903 | 1.000 | 1.000 | 42656 | tags=100%, list=78%, signal=455% | |
144 | G-PROTEIN COUPLED PURINERGIC RECEPTOR SIGNALING PATHWAY | 5 | 0.34 | 0.66 | 0.882 | 1.000 | 1.000 | 36248 | tags=100%, list=66%, signal=297% | |
145 | HISTIDINE METABOLIC PROCESS | 19 | 0.23 | 0.66 | 0.867 | 1.000 | 1.000 | 36319 | tags=95%, list=66%, signal=282% | |
146 | HISTIDINE CATABOLIC PROCESS | 19 | 0.23 | 0.66 | 0.867 | 1.000 | 1.000 | 36319 | tags=95%, list=66%, signal=282% | |
147 | IMIDAZOLE-CONTAINING COMPOUND CATABOLIC PROCESS | 19 | 0.23 | 0.66 | 0.867 | 1.000 | 1.000 | 36319 | tags=95%, list=66%, signal=282% | |
148 | NEGATIVE REGULATION OF BONE REMODELING | 12 | 0.25 | 0.66 | 0.880 | 1.000 | 1.000 | 41224 | tags=100%, list=75%, signal=406% | |
149 | REGULATION OF FEVER GENERATION | 19 | 0.28 | 0.66 | 0.894 | 1.000 | 1.000 | 32399 | tags=95%, list=59%, signal=232% | |
150 | POSITIVE REGULATION OF FEVER GENERATION | 19 | 0.28 | 0.66 | 0.894 | 1.000 | 1.000 | 32399 | tags=95%, list=59%, signal=232% | |
151 | REGULATION OF HEAT GENERATION | 19 | 0.28 | 0.66 | 0.894 | 1.000 | 1.000 | 32399 | tags=95%, list=59%, signal=232% | |
152 | POSITIVE REGULATION OF HEAT GENERATION | 19 | 0.28 | 0.66 | 0.894 | 1.000 | 1.000 | 32399 | tags=95%, list=59%, signal=232% | |
153 | PROTEIN O-LINKED FUCOSYLATION | 36 | 0.20 | 0.65 | 0.903 | 1.000 | 1.000 | 22250 | tags=78%, list=41%, signal=131% | |
154 | SYNCYTIUM FORMATION BY PLASMA MEMBRANE FUSION | 18 | 0.19 | 0.65 | 0.940 | 1.000 | 1.000 | 73 | tags=11%, list=0%, signal=11% | |
155 | POSITIVE REGULATION OF THE FORCE OF HEART CONTRACTION | 23 | 0.21 | 0.65 | 0.879 | 1.000 | 1.000 | 13266 | tags=65%, list=24%, signal=86% | |
156 | REGULATION OF BONE DEVELOPMENT | 7 | 0.29 | 0.65 | 0.896 | 1.000 | 1.000 | 38626 | tags=100%, list=71%, signal=341% | |
157 | NEGATIVE REGULATION OF HEART RATE | 15 | 0.24 | 0.64 | 0.884 | 1.000 | 1.000 | 41701 | tags=100%, list=76%, signal=421% | |
158 | REGULATION OF NK T CELL ACTIVATION | 8 | 0.29 | 0.64 | 0.855 | 1.000 | 1.000 | 38692 | tags=100%, list=71%, signal=342% | |
159 | ELASTIC FIBER ASSEMBLY | 20 | 0.23 | 0.64 | 0.898 | 1.000 | 1.000 | 27839 | tags=85%, list=51%, signal=173% | |
160 | CARDIAC MYOFIBRIL ASSEMBLY | 32 | 0.18 | 0.64 | 0.921 | 1.000 | 1.000 | 33202 | tags=88%, list=61%, signal=223% | |
161 | POSITIVE REGULATION OF ACUTE INFLAMMATORY RESPONSE | 29 | 0.28 | 0.64 | 0.915 | 1.000 | 1.000 | 32633 | tags=93%, list=60%, signal=231% | |
162 | NEGATIVE REGULATION OF BLOOD PRESSURE | 24 | 0.22 | 0.64 | 0.913 | 1.000 | 1.000 | 42707 | tags=100%, list=78%, signal=457% | |
163 | POSITIVE REGULATION OF CHONDROCYTE DIFFERENTIATION | 28 | 0.17 | 0.63 | 0.943 | 1.000 | 1.000 | 32814 | tags=89%, list=60%, signal=223% | |
164 | PERICARDIUM DEVELOPMENT | 14 | 0.22 | 0.63 | 0.899 | 1.000 | 1.000 | 33912 | tags=93%, list=62%, signal=244% | |
165 | RESPONSE TO CGMP | 14 | 0.23 | 0.63 | 0.901 | 1.000 | 1.000 | 42095 | tags=100%, list=77%, signal=435% | |
166 | CELLULAR RESPONSE TO CGMP | 14 | 0.23 | 0.63 | 0.901 | 1.000 | 1.000 | 42095 | tags=100%, list=77%, signal=435% | |
167 | GLOMERULAR BASEMENT MEMBRANE DEVELOPMENT | 20 | 0.21 | 0.63 | 0.897 | 1.000 | 1.000 | 28307 | tags=85%, list=52%, signal=176% | |
168 | REGULATION OF CELL FATE SPECIFICATION | 9 | 0.22 | 0.63 | 0.941 | 1.000 | 1.000 | 42656 | tags=100%, list=78%, signal=455% | |
169 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION OF SMELL | 9 | 0.28 | 0.63 | 0.900 | 1.000 | 1.000 | 13025 | tags=78%, list=24%, signal=102% | |
170 | POLYSACCHARIDE DIGESTION | 5 | 0.29 | 0.62 | 0.940 | 1.000 | 1.000 | 38912 | tags=100%, list=71%, signal=347% | |
171 | PROGESTERONE METABOLIC PROCESS | 20 | 0.22 | 0.62 | 0.879 | 1.000 | 1.000 | 37865 | tags=95%, list=69%, signal=309% | |
172 | REGULATION OF GLUCOCORTICOID BIOSYNTHETIC PROCESS | 14 | 0.23 | 0.62 | 0.899 | 1.000 | 1.000 | 34096 | tags=93%, list=62%, signal=247% | |
173 | NEGATIVE REGULATION OF HORMONE BIOSYNTHETIC PROCESS | 14 | 0.23 | 0.62 | 0.899 | 1.000 | 1.000 | 34096 | tags=93%, list=62%, signal=247% | |
174 | REGULATION OF CORTISOL BIOSYNTHETIC PROCESS | 14 | 0.23 | 0.62 | 0.899 | 1.000 | 1.000 | 34096 | tags=93%, list=62%, signal=247% | |
175 | EXOGENOUS DRUG CATABOLIC PROCESS | 32 | 0.18 | 0.62 | 0.924 | 1.000 | 1.000 | 36567 | tags=91%, list=67%, signal=273% | |
176 | POSITIVE REGULATION OF CARTILAGE DEVELOPMENT | 43 | 0.16 | 0.61 | 0.925 | 1.000 | 1.000 | 27358 | tags=81%, list=50%, signal=163% | |
177 | GLUCOCORTICOID BIOSYNTHETIC PROCESS | 13 | 0.23 | 0.61 | 0.928 | 1.000 | 1.000 | 15121 | tags=77%, list=28%, signal=106% | |
178 | MATING | 13 | 0.23 | 0.61 | 0.898 | 1.000 | 1.000 | 27044 | tags=85%, list=49%, signal=167% | |
179 | POSITIVE REGULATION OF CATECHOLAMINE SECRETION | 11 | 0.24 | 0.61 | 0.919 | 1.000 | 1.000 | 438 | tags=18%, list=1%, signal=18% | |
180 | PATTERNING OF BLOOD VESSELS | 22 | 0.20 | 0.61 | 0.900 | 1.000 | 1.000 | 43701 | tags=100%, list=80%, signal=498% | |
181 | CEREBELLAR GRANULAR LAYER DEVELOPMENT | 15 | 0.22 | 0.61 | 0.927 | 1.000 | 1.000 | 42615 | tags=100%, list=78%, signal=453% | |
182 | DRUG CATABOLIC PROCESS | 39 | 0.16 | 0.60 | 0.931 | 1.000 | 1.000 | 36567 | tags=90%, list=67%, signal=271% | |
183 | SARCOMERE ORGANIZATION | 37 | 0.17 | 0.60 | 0.947 | 1.000 | 1.000 | 45463 | tags=100%, list=83%, signal=593% | |
184 | MEMBRANE TO MEMBRANE DOCKING | 14 | 0.23 | 0.60 | 0.903 | 1.000 | 1.000 | 34170 | tags=93%, list=62%, signal=248% | |
185 | CEREBELLAR GRANULAR LAYER MORPHOGENESIS | 13 | 0.22 | 0.59 | 0.931 | 1.000 | 1.000 | 42615 | tags=100%, list=78%, signal=453% | |
186 | SECONDARY METABOLITE BIOSYNTHETIC PROCESS | 15 | 0.21 | 0.59 | 0.932 | 1.000 | 1.000 | 24486 | tags=80%, list=45%, signal=145% | |
187 | MUSCLE CELL FATE COMMITMENT | 20 | 0.21 | 0.59 | 0.915 | 1.000 | 1.000 | 27188 | tags=85%, list=50%, signal=169% | |
188 | REGULATION OF GLOMERULAR MESANGIAL CELL PROLIFERATION | 14 | 0.24 | 0.59 | 0.917 | 1.000 | 1.000 | 18499 | tags=71%, list=34%, signal=108% | |
189 | REGULATION OF CARDIAC MUSCLE CONTRACTION BY REGULATION OF THE RELEASE OF SEQUESTERED CALCIUM ION | 46 | 0.16 | 0.59 | 0.965 | 1.000 | 1.000 | 43511 | tags=98%, list=80%, signal=479% | |
190 | CATECHOL-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 23 | 0.19 | 0.59 | 0.935 | 1.000 | 1.000 | 44315 | tags=100%, list=81%, signal=528% | |
191 | CATECHOLAMINE BIOSYNTHETIC PROCESS | 23 | 0.19 | 0.59 | 0.935 | 1.000 | 1.000 | 44315 | tags=100%, list=81%, signal=528% | |
192 | REGULATION OF DOPAMINE METABOLIC PROCESS | 10 | 0.22 | 0.58 | 0.936 | 1.000 | 1.000 | 1914 | tags=30%, list=4%, signal=31% | |
193 | REGULATION OF CATECHOLAMINE METABOLIC PROCESS | 10 | 0.22 | 0.58 | 0.936 | 1.000 | 1.000 | 1914 | tags=30%, list=4%, signal=31% | |
194 | REGULATION OF FERTILIZATION | 6 | 0.26 | 0.58 | 0.944 | 1.000 | 1.000 | 40370 | tags=100%, list=74%, signal=382% | |
195 | LEUKEMIA INHIBITORY FACTOR SIGNALING PATHWAY | 13 | 0.25 | 0.58 | 0.875 | 1.000 | 1.000 | 30964 | tags=92%, list=57%, signal=213% | |
196 | NEGATIVE REGULATION OF INTERLEUKIN-17 PRODUCTION | 15 | 0.24 | 0.58 | 0.887 | 1.000 | 1.000 | 34148 | tags=93%, list=62%, signal=249% | |
197 | REGULATION OF BILE ACID METABOLIC PROCESS | 22 | 0.19 | 0.58 | 0.924 | 1.000 | 1.000 | 44368 | tags=100%, list=81%, signal=530% | |
198 | DETECTION OF MECHANICAL STIMULUS | 31 | 0.16 | 0.57 | 0.959 | 1.000 | 1.000 | 42392 | tags=97%, list=78%, signal=431% | |
199 | MALE MEIOSIS | 27 | 0.18 | 0.57 | 0.938 | 1.000 | 1.000 | 35316 | tags=93%, list=65%, signal=261% | |
200 | REGULATION OF SMOOTH MUSCLE CELL APOPTOTIC PROCESS | 17 | 0.19 | 0.57 | 0.945 | 1.000 | 1.000 | 44368 | tags=100%, list=81%, signal=530% | |
201 | STRIATED MUSCLE CELL PROLIFERATION | 15 | 0.20 | 0.57 | 0.955 | 1.000 | 1.000 | 372 | tags=13%, list=1%, signal=13% | |
202 | TACHYKININ RECEPTOR SIGNALING PATHWAY | 13 | 0.22 | 0.56 | 0.942 | 1.000 | 1.000 | 34534 | tags=92%, list=63%, signal=251% | |
203 | REGULATION OF VASOCONSTRICTION | 41 | 0.17 | 0.56 | 0.983 | 1.000 | 1.000 | 39569 | tags=95%, list=72%, signal=344% | |
204 | REGULATION OF NEURONAL SYNAPTIC PLASTICITY | 45 | 0.16 | 0.56 | 0.963 | 1.000 | 1.000 | 1077 | tags=16%, list=2%, signal=16% | |
205 | REGULATION OF CGMP METABOLIC PROCESS | 32 | 0.18 | 0.56 | 0.942 | 1.000 | 1.000 | 27854 | tags=81%, list=51%, signal=166% | |
206 | REGULATION OF MONONUCLEAR CELL MIGRATION | 19 | 0.20 | 0.56 | 0.961 | 1.000 | 1.000 | 20184 | tags=74%, list=37%, signal=117% | |
207 | DOPAMINE BIOSYNTHETIC PROCESS | 13 | 0.22 | 0.55 | 0.921 | 1.000 | 1.000 | 42776 | tags=100%, list=78%, signal=459% | |
208 | REGULATION OF ANTIGEN PROCESSING AND PRESENTATION OF PEPTIDE OR POLYSACCHARIDE ANTIGEN VIA MHC CLASS II | 16 | 0.22 | 0.55 | 0.932 | 1.000 | 1.000 | 20184 | tags=75%, list=37%, signal=119% | |
209 | POSITIVE REGULATION OF OSTEOBLAST PROLIFERATION | 9 | 0.23 | 0.55 | 0.951 | 1.000 | 1.000 | 42369 | tags=100%, list=77%, signal=444% | |
210 | REGULATION OF THE FORCE OF HEART CONTRACTION | 47 | 0.14 | 0.55 | 0.979 | 1.000 | 1.000 | 316 | tags=9%, list=1%, signal=9% | |
211 | COLLAGEN FIBRIL ORGANIZATION | 56 | 0.14 | 0.54 | 0.969 | 1.000 | 1.000 | 43297 | tags=96%, list=79%, signal=463% | |
212 | POSITIVE REGULATION OF ACTIVATION OF JANUS KINASE ACTIVITY | 20 | 0.21 | 0.54 | 0.933 | 1.000 | 1.000 | 1928 | tags=35%, list=4%, signal=36% | |
213 | EXCITATORY POSTSYNAPTIC POTENTIAL | 20 | 0.18 | 0.54 | 0.967 | 1.000 | 1.000 | 1122 | tags=20%, list=2%, signal=20% | |
214 | MONOAMINE TRANSPORT | 25 | 0.18 | 0.54 | 0.958 | 1.000 | 1.000 | 19381 | tags=76%, list=35%, signal=118% | |
215 | NEGATIVE REGULATION OF OSTEOCLAST DIFFERENTIATION | 26 | 0.20 | 0.54 | 0.927 | 1.000 | 1.000 | 25082 | tags=85%, list=46%, signal=156% | |
216 | REGULATION OF NATURAL KILLER CELL PROLIFERATION | 8 | 0.23 | 0.53 | 0.970 | 1.000 | 1.000 | 41866 | tags=100%, list=77%, signal=427% | |
217 | SMOOTH MUSCLE CONTRACTION | 82 | 0.13 | 0.53 | 0.984 | 1.000 | 1.000 | 44864 | tags=98%, list=82%, signal=543% | |
218 | GLANDULAR EPITHELIAL CELL DIFFERENTIATION | 38 | 0.16 | 0.53 | 0.951 | 1.000 | 1.000 | 46168 | tags=100%, list=84%, signal=642% | |
219 | MOTOR NEURON AXON GUIDANCE | 16 | 0.18 | 0.53 | 0.972 | 1.000 | 1.000 | 22839 | tags=81%, list=42%, signal=139% | |
220 | DNA CYTOSINE DEAMINATION | 7 | 0.22 | 0.53 | 0.984 | 1.000 | 1.000 | 14 | tags=14%, list=0%, signal=14% | |
221 | REGULATION OF ACTIVATION OF JANUS KINASE ACTIVITY | 23 | 0.20 | 0.52 | 0.950 | 1.000 | 1.000 | 16984 | tags=78%, list=31%, signal=113% | |
222 | OLFACTORY BULB DEVELOPMENT | 25 | 0.17 | 0.52 | 0.975 | 1.000 | 1.000 | 37365 | tags=92%, list=68%, signal=290% | |
223 | OLFACTORY LOBE DEVELOPMENT | 25 | 0.17 | 0.52 | 0.975 | 1.000 | 1.000 | 37365 | tags=92%, list=68%, signal=290% | |
224 | REGULATION OF BILE ACID BIOSYNTHETIC PROCESS | 16 | 0.19 | 0.52 | 0.954 | 1.000 | 1.000 | 29728 | tags=88%, list=54%, signal=192% | |
225 | REGULATION OF MYOSIN-LIGHT-CHAIN-PHOSPHATASE ACTIVITY | 15 | 0.20 | 0.52 | 0.919 | 1.000 | 1.000 | 32184 | tags=87%, list=59%, signal=211% | |
226 | CITRULLINE BIOSYNTHETIC PROCESS | 9 | 0.23 | 0.52 | 0.972 | 1.000 | 1.000 | 42350 | tags=100%, list=77%, signal=444% | |
227 | POSITIVE REGULATION OF CGMP BIOSYNTHETIC PROCESS | 14 | 0.20 | 0.51 | 0.962 | 1.000 | 1.000 | 21509 | tags=79%, list=39%, signal=129% | |
228 | HYALURONAN BIOSYNTHETIC PROCESS | 12 | 0.21 | 0.51 | 0.986 | 1.000 | 1.000 | 34447 | tags=92%, list=63%, signal=248% | |
229 | NEUROTRANSMITTER-GATED ION CHANNEL CLUSTERING | 15 | 0.19 | 0.51 | 0.970 | 1.000 | 1.000 | 24855 | tags=80%, list=45%, signal=147% | |
230 | CEREBELLAR CORTEX FORMATION | 20 | 0.16 | 0.51 | 0.986 | 1.000 | 1.000 | 45979 | tags=100%, list=84%, signal=629% | |
231 | NEGATIVE REGULATION OF HETEROTYPIC CELL-CELL ADHESION | 20 | 0.20 | 0.51 | 0.961 | 1.000 | 1.000 | 43904 | tags=100%, list=80%, signal=507% | |
232 | REGULATION OF CELL-CELL ADHESION INVOLVED IN GASTRULATION | 20 | 0.20 | 0.51 | 0.961 | 1.000 | 1.000 | 43904 | tags=100%, list=80%, signal=507% | |
233 | REGULATION OF INSULIN-LIKE GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 38 | 0.14 | 0.51 | 0.994 | 1.000 | 1.000 | 1928 | tags=21%, list=4%, signal=22% | |
234 | MYOTUBE DIFFERENTIATION | 40 | 0.13 | 0.51 | 0.988 | 1.000 | 1.000 | 80 | tags=8%, list=0%, signal=8% | |
235 | REGULATION OF LONG-TERM NEURONAL SYNAPTIC PLASTICITY | 22 | 0.18 | 0.50 | 0.961 | 1.000 | 1.000 | 901 | tags=18%, list=2%, signal=18% | |
236 | PHOTORECEPTOR CELL DEVELOPMENT | 29 | 0.16 | 0.50 | 0.976 | 1.000 | 1.000 | 30403 | tags=86%, list=56%, signal=194% | |
237 | POSITIVE REGULATION OF SPROUTING ANGIOGENESIS | 30 | 0.16 | 0.50 | 0.977 | 1.000 | 1.000 | 30175 | tags=83%, list=55%, signal=186% | |
238 | REGULATION OF WATER LOSS VIA SKIN | 22 | 0.17 | 0.50 | 0.975 | 1.000 | 1.000 | 31069 | tags=86%, list=57%, signal=200% | |
239 | ESTABLISHMENT OF SKIN BARRIER | 22 | 0.17 | 0.50 | 0.975 | 1.000 | 1.000 | 31069 | tags=86%, list=57%, signal=200% | |
240 | ANTIFUNGAL HUMORAL RESPONSE | 14 | 0.18 | 0.50 | 0.979 | 1.000 | 1.000 | 44997 | tags=100%, list=82%, signal=565% | |
241 | CELL PROLIFERATION INVOLVED IN KIDNEY DEVELOPMENT | 13 | 0.20 | 0.50 | 0.975 | 1.000 | 1.000 | 43701 | tags=100%, list=80%, signal=498% | |
242 | REGULATION OF CELL-CELL ADHESION MEDIATED BY INTEGRIN | 14 | 0.19 | 0.50 | 0.960 | 1.000 | 1.000 | 36499 | tags=93%, list=67%, signal=279% | |
243 | SYNAPTIC TRANSMISSION, CHOLINERGIC | 26 | 0.16 | 0.50 | 0.978 | 1.000 | 1.000 | 438 | tags=12%, list=1%, signal=12% | |
244 | REGULATION OF ACROSOME REACTION | 12 | 0.19 | 0.49 | 0.971 | 1.000 | 1.000 | 35283 | tags=92%, list=65%, signal=258% | |
245 | RESPONSE TO PLATELET-DERIVED GROWTH FACTOR | 15 | 0.16 | 0.49 | 0.988 | 1.000 | 1.000 | 25246 | tags=80%, list=46%, signal=149% | |
246 | NEGATIVE REGULATION OF NEUROTRANSMITTER TRANSPORT | 24 | 0.14 | 0.49 | 0.994 | 1.000 | 1.000 | 73 | tags=8%, list=0%, signal=8% | |
247 | INTERMEDIATE FILAMENT ORGANIZATION | 24 | 0.15 | 0.49 | 0.978 | 1.000 | 1.000 | 40913 | tags=96%, list=75%, signal=381% | |
248 | MULTICELLULAR ORGANISMAL RESPONSE TO STRESS | 37 | 0.15 | 0.49 | 0.982 | 1.000 | 1.000 | 834 | tags=14%, list=2%, signal=14% | |
249 | MUSCLE CELL PROLIFERATION | 19 | 0.16 | 0.49 | 0.980 | 1.000 | 1.000 | 372 | tags=11%, list=1%, signal=11% | |
250 | RESPONSE TO COCAINE | 13 | 0.19 | 0.48 | 0.972 | 1.000 | 1.000 | 1321 | tags=23%, list=2%, signal=24% | |
251 | KILLING OF CELLS OF OTHER ORGANISM | 8 | 0.20 | 0.48 | 0.982 | 1.000 | 1.000 | 43545 | tags=100%, list=80%, signal=491% | |
252 | DISRUPTION OF CELLS OF OTHER ORGANISM | 8 | 0.20 | 0.48 | 0.982 | 1.000 | 1.000 | 43545 | tags=100%, list=80%, signal=491% | |
253 | MONOVALENT INORGANIC ANION HOMEOSTASIS | 32 | 0.16 | 0.48 | 0.974 | 1.000 | 1.000 | 36947 | tags=91%, list=68%, signal=279% | |
254 | REGULATION OF ANTIMICROBIAL HUMORAL RESPONSE | 7 | 0.21 | 0.48 | 0.983 | 1.000 | 1.000 | 22004 | tags=86%, list=40%, signal=143% | |
255 | POSITIVE REGULATION OF ANTIMICROBIAL HUMORAL RESPONSE | 7 | 0.21 | 0.48 | 0.983 | 1.000 | 1.000 | 22004 | tags=86%, list=40%, signal=143% | |
256 | PHASIC SMOOTH MUSCLE CONTRACTION | 17 | 0.18 | 0.48 | 0.978 | 1.000 | 1.000 | 44864 | tags=100%, list=82%, signal=557% | |
257 | IONOTROPIC GLUTAMATE RECEPTOR SIGNALING PATHWAY | 58 | 0.13 | 0.48 | 0.981 | 1.000 | 1.000 | 28382 | tags=83%, list=52%, signal=172% | |
258 | CHEMICAL SYNAPTIC TRANSMISSION, POSTSYNAPTIC | 82 | 0.14 | 0.48 | 0.977 | 1.000 | 1.000 | 31302 | tags=85%, list=57%, signal=199% | |
259 | RESPONSE TO INTERLEUKIN-2 | 12 | 0.19 | 0.48 | 0.983 | 1.000 | 1.000 | 35238 | tags=92%, list=64%, signal=258% | |
260 | ONE-CARBON COMPOUND TRANSPORT | 9 | 0.20 | 0.47 | 0.977 | 1.000 | 1.000 | 31612 | tags=89%, list=58%, signal=211% | |
261 | MEMBRANE DEPOLARIZATION DURING CARDIAC MUSCLE CELL ACTION POTENTIAL | 30 | 0.14 | 0.47 | 0.977 | 1.000 | 1.000 | 46938 | tags=100%, list=86%, signal=706% | |
262 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT3 PROTEIN | 51 | 0.12 | 0.47 | 0.987 | 1.000 | 1.000 | 45771 | tags=98%, list=84%, signal=601% | |
263 | REGULATION OF CATECHOLAMINE SECRETION | 35 | 0.14 | 0.46 | 0.990 | 1.000 | 1.000 | 1321 | tags=14%, list=2%, signal=15% | |
264 | FORELIMB MORPHOGENESIS | 27 | 0.15 | 0.46 | 0.989 | 1.000 | 1.000 | 36987 | tags=93%, list=68%, signal=286% | |
265 | CARDIAC MUSCLE CELL DEVELOPMENT | 82 | 0.11 | 0.46 | 0.992 | 1.000 | 1.000 | 45708 | tags=98%, list=84%, signal=594% | |
266 | POSITIVE REGULATION OF ACROSOME REACTION | 11 | 0.17 | 0.46 | 0.989 | 1.000 | 1.000 | 45116 | tags=100%, list=83%, signal=572% | |
267 | NEGATIVE REGULATION OF MICROTUBULE POLYMERIZATION | 21 | 0.15 | 0.46 | 0.996 | 1.000 | 1.000 | 40547 | tags=95%, list=74%, signal=368% | |
268 | CERAMIDE BIOSYNTHETIC PROCESS | 30 | 0.13 | 0.45 | 0.994 | 1.000 | 1.000 | 47653 | tags=100%, list=87%, signal=778% | |
269 | VOCALIZATION BEHAVIOR | 37 | 0.13 | 0.45 | 0.988 | 1.000 | 1.000 | 26902 | tags=78%, list=49%, signal=154% | |
270 | T CELL LINEAGE COMMITMENT | 14 | 0.19 | 0.45 | 0.973 | 1.000 | 1.000 | 44053 | tags=100%, list=81%, signal=515% | |
271 | CD4-POSITIVE OR CD8-POSITIVE, ALPHA-BETA T CELL LINEAGE COMMITMENT | 14 | 0.19 | 0.45 | 0.973 | 1.000 | 1.000 | 44053 | tags=100%, list=81%, signal=515% | |
272 | REGULATION OF CYTOKINE SECRETION INVOLVED IN IMMUNE RESPONSE | 13 | 0.19 | 0.45 | 0.984 | 1.000 | 1.000 | 35891 | tags=92%, list=66%, signal=269% | |
273 | RESPONSE TO ETHANOL | 37 | 0.14 | 0.45 | 0.992 | 1.000 | 1.000 | 1630 | tags=16%, list=3%, signal=17% | |
274 | LACTATE TRANSPORT | 13 | 0.17 | 0.44 | 0.996 | 1.000 | 1.000 | 37386 | tags=92%, list=68%, signal=292% | |
275 | NEGATIVE REGULATION OF MYOSIN-LIGHT-CHAIN-PHOSPHATASE ACTIVITY | 11 | 0.18 | 0.44 | 0.984 | 1.000 | 1.000 | 33 | tags=9%, list=0%, signal=9% | |
276 | REGULATION OF MACROPHAGE CHEMOTAXIS | 19 | 0.17 | 0.44 | 0.996 | 1.000 | 1.000 | 20184 | tags=74%, list=37%, signal=117% | |
277 | POSITIVE T CELL SELECTION | 19 | 0.19 | 0.44 | 0.964 | 1.000 | 1.000 | 44053 | tags=100%, list=81%, signal=515% | |
278 | POSITIVE REGULATION OF CGMP METABOLIC PROCESS | 18 | 0.16 | 0.44 | 0.982 | 1.000 | 1.000 | 46040 | tags=100%, list=84%, signal=633% | |
279 | ALPHA-BETA T CELL LINEAGE COMMITMENT | 12 | 0.19 | 0.44 | 0.983 | 1.000 | 1.000 | 44053 | tags=100%, list=81%, signal=515% | |
280 | CD4-POSITIVE, ALPHA-BETA T CELL LINEAGE COMMITMENT | 12 | 0.19 | 0.44 | 0.983 | 1.000 | 1.000 | 44053 | tags=100%, list=81%, signal=515% | |
281 | GLUCOCORTICOID METABOLIC PROCESS | 16 | 0.15 | 0.44 | 0.996 | 1.000 | 1.000 | 15136 | tags=69%, list=28%, signal=95% | |
282 | EMBRYONIC DIGIT MORPHOGENESIS | 36 | 0.14 | 0.44 | 0.991 | 1.000 | 1.000 | 22207 | tags=75%, list=41%, signal=126% | |
283 | NEGATIVE REGULATION OF CARDIAC MUSCLE CELL APOPTOTIC PROCESS | 8 | 0.20 | 0.43 | 0.988 | 1.000 | 1.000 | 26639 | tags=88%, list=49%, signal=171% | |
284 | GAMMA-AMINOBUTYRIC ACID SIGNALING PATHWAY | 15 | 0.16 | 0.43 | 0.992 | 1.000 | 1.000 | 31149 | tags=87%, list=57%, signal=201% | |
285 | POSITIVE REGULATION OF CELL MIGRATION INVOLVED IN SPROUTING ANGIOGENESIS | 17 | 0.16 | 0.43 | 0.987 | 1.000 | 1.000 | 39271 | tags=94%, list=72%, signal=334% | |
286 | RETINA VASCULATURE DEVELOPMENT IN CAMERA-TYPE EYE | 29 | 0.14 | 0.42 | 0.990 | 1.000 | 1.000 | 42604 | tags=97%, list=78%, signal=437% | |
287 | REGULATION OF INTERLEUKIN-2 BIOSYNTHETIC PROCESS | 16 | 0.18 | 0.42 | 0.996 | 1.000 | 1.000 | 25313 | tags=81%, list=46%, signal=151% | |
288 | NEUROLOGICAL SYSTEM PROCESS INVOLVED IN REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE | 16 | 0.17 | 0.42 | 0.994 | 1.000 | 1.000 | 45272 | tags=100%, list=83%, signal=581% | |
289 | CELLULAR POTASSIUM ION TRANSPORT | 172 | 0.10 | 0.41 | 0.998 | 1.000 | 1.000 | 577 | tags=7%, list=1%, signal=7% | |
290 | POTASSIUM ION TRANSMEMBRANE TRANSPORT | 172 | 0.10 | 0.41 | 0.998 | 1.000 | 1.000 | 577 | tags=7%, list=1%, signal=7% | |
291 | CHEMOKINE-MEDIATED SIGNALING PATHWAY | 43 | 0.14 | 0.41 | 0.984 | 1.000 | 1.000 | 22665 | tags=74%, list=41%, signal=127% | |
292 | DETECTION OF STIMULUS INVOLVED IN SENSORY PERCEPTION | 81 | 0.11 | 0.41 | 0.981 | 1.000 | 1.000 | 40637 | tags=93%, list=74%, signal=360% | |
293 | REGULATION OF FIBRINOLYSIS | 28 | 0.14 | 0.40 | 0.990 | 1.000 | 1.000 | 29671 | tags=82%, list=54%, signal=180% | |
294 | RESPONSE TO MUSCLE STRETCH | 29 | 0.12 | 0.40 | 0.989 | 1.000 | 1.000 | 43511 | tags=97%, list=80%, signal=473% | |
295 | EXTRACELLULAR MATRIX ASSEMBLY | 35 | 0.11 | 0.40 | 0.996 | 1.000 | 1.000 | 1619 | tags=14%, list=3%, signal=15% | |
296 | RESPONSE TO AMMONIUM ION | 43 | 0.12 | 0.39 | 0.996 | 1.000 | 1.000 | 29900 | tags=81%, list=55%, signal=179% | |
297 | POSITIVE REGULATION OF NITRIC-OXIDE SYNTHASE BIOSYNTHETIC PROCESS | 18 | 0.23 | 0.39 | 0.993 | 1.000 | 1.000 | 42112 | tags=100%, list=77%, signal=435% | |
298 | AZOLE TRANSPORT | 10 | 0.15 | 0.39 | 0.996 | 1.000 | 1.000 | 16437 | tags=70%, list=30%, signal=100% | |
299 | NEGATIVE REGULATION OF CYCLIC NUCLEOTIDE BIOSYNTHETIC PROCESS | 46 | 0.12 | 0.39 | 0.998 | 1.000 | 1.000 | 2031 | tags=15%, list=4%, signal=16% | |
300 | SOMITOGENESIS | 10 | 0.15 | 0.39 | 0.996 | 1.000 | 1.000 | 10450 | tags=60%, list=19%, signal=74% | |
301 | POSITIVE REGULATION OF MYOBLAST FUSION | 20 | 0.18 | 0.38 | 0.992 | 1.000 | 1.000 | 19353 | tags=70%, list=35%, signal=108% | |
302 | POSITIVE REGULATION OF SYNCYTIUM FORMATION BY PLASMA MEMBRANE FUSION | 28 | 0.15 | 0.38 | 0.994 | 1.000 | 1.000 | 19421 | tags=68%, list=36%, signal=105% | |
303 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION | 45 | 0.11 | 0.38 | 0.990 | 1.000 | 1.000 | 40637 | tags=93%, list=74%, signal=363% | |
304 | SENSORY PERCEPTION OF PAIN | 38 | 0.12 | 0.38 | 0.996 | 1.000 | 1.000 | 596 | tags=11%, list=1%, signal=11% | |
305 | REGULATION OF CARDIAC MUSCLE CELL APOPTOTIC PROCESS | 17 | 0.13 | 0.38 | 1.000 | 1.000 | 1.000 | 47505 | tags=100%, list=87%, signal=762% | |
306 | MYELOID DENDRITIC CELL DIFFERENTIATION | 16 | 0.13 | 0.37 | 1.000 | 1.000 | 1.000 | 47767 | tags=100%, list=87%, signal=791% | |
307 | POTASSIUM ION TRANSPORT | 193 | 0.09 | 0.37 | 0.996 | 1.000 | 1.000 | 577 | tags=6%, list=1%, signal=6% | |
308 | REGULATION OF TUBE SIZE | 114 | 0.09 | 0.36 | 0.998 | 1.000 | 1.000 | 48459 | tags=99%, list=89%, signal=870% | |
309 | REGULATION OF BLOOD VESSEL SIZE | 114 | 0.09 | 0.36 | 0.998 | 1.000 | 1.000 | 48459 | tags=99%, list=89%, signal=870% | |
310 | ALKALOID METABOLIC PROCESS | 24 | 0.15 | 0.36 | 1.000 | 1.000 | 1.000 | 24906 | tags=79%, list=46%, signal=145% | |
311 | NEGATIVE REGULATION OF CYCLASE ACTIVITY | 38 | 0.11 | 0.36 | 1.000 | 1.000 | 1.000 | 1668 | tags=13%, list=3%, signal=14% | |
312 | NEGATIVE REGULATION OF COAGULATION | 75 | 0.11 | 0.36 | 0.984 | 1.000 | 1.000 | 44005 | tags=96%, list=80%, signal=491% | |
313 | NEGATIVE REGULATION OF CYCLIC NUCLEOTIDE METABOLIC PROCESS | 50 | 0.10 | 0.36 | 1.000 | 1.000 | 1.000 | 1668 | tags=12%, list=3%, signal=12% | |
314 | REGULATION OF NEUROTRANSMITTER UPTAKE | 34 | 0.10 | 0.35 | 0.998 | 1.000 | 1.000 | 73 | tags=6%, list=0%, signal=6% | |
315 | NEGATIVE REGULATION OF B CELL ACTIVATION | 41 | 0.13 | 0.35 | 0.992 | 1.000 | 1.000 | 41224 | tags=95%, list=75%, signal=386% | |
316 | NEGATIVE REGULATION OF BLOOD COAGULATION | 73 | 0.11 | 0.35 | 0.992 | 1.000 | 1.000 | 44005 | tags=96%, list=80%, signal=491% | |
317 | NEGATIVE REGULATION OF HEMOSTASIS | 73 | 0.11 | 0.35 | 0.992 | 1.000 | 1.000 | 44005 | tags=96%, list=80%, signal=491% | |
318 | MUSCLE FIBER DEVELOPMENT | 35 | 0.10 | 0.34 | 1.000 | 1.000 | 1.000 | 40197 | tags=91%, list=74%, signal=345% | |
319 | ADULT BEHAVIOR | 93 | 0.08 | 0.33 | 1.000 | 1.000 | 1.000 | 47692 | tags=98%, list=87%, signal=765% | |
320 | NEGATIVE REGULATION OF MUSCLE CONTRACTION | 27 | 0.11 | 0.32 | 1.000 | 1.000 | 1.000 | 1745 | tags=15%, list=3%, signal=15% | |
321 | CELL DIFFERENTIATION INVOLVED IN METANEPHROS DEVELOPMENT | 16 | 0.13 | 0.32 | 1.000 | 1.000 | 1.000 | 40617 | tags=94%, list=74%, signal=365% | |
322 | CELLULAR RESPONSE TO GONADOTROPIN STIMULUS | 16 | 0.11 | 0.30 | 1.000 | 1.000 | 1.000 | 66 | tags=6%, list=0%, signal=6% | |
323 | B CELL MEDIATED IMMUNITY | 117 | 0.07 | 0.24 | 1.000 | 1.000 | 1.000 | 38814 | tags=90%, list=71%, signal=309% | |
324 | IMMUNOGLOBULIN MEDIATED IMMUNE RESPONSE | 115 | 0.07 | 0.22 | 1.000 | 1.000 | 1.000 | 38814 | tags=90%, list=71%, signal=308% | |
325 | COMPLEMENT ACTIVATION | 110 | 0.06 | 0.19 | 1.000 | 1.000 | 1.000 | 34430 | tags=85%, list=63%, signal=228% |