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 | DORSAL/VENTRAL AXIS SPECIFICATION | Details ... | 14 | -0.71 | -1.91 | 0.002 | 1.000 | 0.574 | 1470 | tags=36%, list=7%, signal=38% |
2 | PRIMARY ALCOHOL METABOLIC PROCESS | Details ... | 27 | -0.56 | -1.89 | 0.000 | 1.000 | 0.637 | 4845 | tags=52%, list=24%, signal=68% |
3 | REGULATION OF CHONDROCYTE DIFFERENTIATION | Details ... | 19 | -0.66 | -1.89 | 0.002 | 0.782 | 0.644 | 3245 | tags=58%, list=16%, signal=69% |
4 | POSITIVE REGULATION OF CHONDROCYTE DIFFERENTIATION | Details ... | 9 | -0.82 | -1.88 | 0.000 | 0.669 | 0.693 | 3245 | tags=78%, list=16%, signal=92% |
5 | POSITIVE REGULATION OF CAMP BIOSYNTHETIC PROCESS | Details ... | 50 | -0.54 | -1.87 | 0.000 | 0.654 | 0.759 | 5931 | tags=54%, list=29%, signal=76% |
6 | POSITIVE REGULATION OF CYCLIC NUCLEOTIDE BIOSYNTHETIC PROCESS | Details ... | 57 | -0.54 | -1.86 | 0.002 | 0.563 | 0.768 | 5931 | tags=54%, list=29%, signal=76% |
7 | POSITIVE REGULATION OF ADENYLATE CYCLASE ACTIVITY | Details ... | 27 | -0.60 | -1.86 | 0.004 | 0.492 | 0.772 | 3717 | tags=52%, list=18%, signal=63% |
8 | ORGAN INDUCTION | Details ... | 19 | -0.63 | -1.84 | 0.004 | 0.605 | 0.849 | 4215 | tags=53%, list=20%, signal=66% |
9 | REGULATION OF CARBOHYDRATE BIOSYNTHETIC PROCESS | Details ... | 38 | -0.54 | -1.84 | 0.004 | 0.544 | 0.850 | 4049 | tags=42%, list=20%, signal=52% |
10 | POSITIVE REGULATION OF SMOOTHENED SIGNALING PATHWAY | Details ... | 9 | -0.80 | -1.81 | 0.000 | 0.667 | 0.910 | 2803 | tags=78%, list=14%, signal=90% |
11 | POSITIVE REGULATION OF LYASE ACTIVITY | Details ... | 34 | -0.56 | -1.81 | 0.004 | 0.614 | 0.913 | 4575 | tags=56%, list=22%, signal=72% |
12 | NEGATIVE REGULATION OF MICROTUBULE POLYMERIZATION | Details ... | 5 | -0.87 | -1.81 | 0.000 | 0.597 | 0.923 | 212 | tags=40%, list=1%, signal=40% |
13 | SOMATIC MOTOR NEURON DIFFERENTIATION | Details ... | 5 | -0.86 | -1.80 | 0.002 | 0.583 | 0.932 | 1271 | tags=20%, list=6%, signal=21% |
14 | POSITIVE REGULATION OF NUCLEOTIDE BIOSYNTHETIC PROCESS | Details ... | 60 | -0.52 | -1.80 | 0.000 | 0.566 | 0.936 | 5931 | tags=53%, list=29%, signal=75% |
15 | POSITIVE REGULATION OF PURINE NUCLEOTIDE BIOSYNTHETIC PROCESS | Details ... | 60 | -0.52 | -1.80 | 0.000 | 0.528 | 0.936 | 5931 | tags=53%, list=29%, signal=75% |
16 | MODULATION BY HOST OF VIRAL RELEASE FROM HOST CELL | Details ... | 5 | -0.84 | -1.79 | 0.004 | 0.508 | 0.937 | 1357 | tags=40%, list=7%, signal=43% |
17 | POSITIVE REGULATION BY HOST OF VIRAL RELEASE FROM HOST CELL | Details ... | 5 | -0.84 | -1.79 | 0.004 | 0.478 | 0.937 | 1357 | tags=40%, list=7%, signal=43% |
18 | PHOTOTRANSDUCTION | Details ... | 91 | -0.47 | -1.79 | 0.004 | 0.467 | 0.943 | 5485 | tags=43%, list=27%, signal=58% |
19 | NEGATIVE REGULATION OF T CELL APOPTOTIC PROCESS | Details ... | 7 | -0.83 | -1.79 | 0.000 | 0.456 | 0.945 | 1523 | tags=43%, list=7%, signal=46% |
20 | ACTIVATION OF ADENYLATE CYCLASE ACTIVITY | Details ... | 24 | -0.61 | -1.79 | 0.004 | 0.437 | 0.946 | 3717 | tags=54%, list=18%, signal=66% |
21 | NEGATIVE REGULATION OF PLATELET-DERIVED GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 9 | -0.70 | -1.78 | 0.006 | 0.446 | 0.949 | 792 | tags=33%, list=4%, signal=35% | |
22 | PHOTOTRANSDUCTION, VISIBLE LIGHT | 85 | -0.46 | -1.77 | 0.004 | 0.470 | 0.960 | 5485 | tags=42%, list=27%, signal=57% | |
23 | NOTOCHORD DEVELOPMENT | 16 | -0.65 | -1.77 | 0.008 | 0.458 | 0.961 | 3799 | tags=63%, list=18%, signal=77% | |
24 | APICAL JUNCTION ASSEMBLY | 35 | -0.53 | -1.77 | 0.004 | 0.449 | 0.965 | 3445 | tags=43%, list=17%, signal=51% | |
25 | TRIGLYCERIDE CATABOLIC PROCESS | 21 | -0.60 | -1.76 | 0.006 | 0.465 | 0.971 | 4193 | tags=52%, list=20%, signal=66% | |
26 | DEVELOPMENTAL INDUCTION | 32 | -0.53 | -1.76 | 0.004 | 0.484 | 0.978 | 5056 | tags=44%, list=25%, signal=58% | |
27 | REGULATION OF CARTILAGE DEVELOPMENT | 23 | -0.58 | -1.76 | 0.004 | 0.479 | 0.979 | 3245 | tags=52%, list=16%, signal=62% | |
28 | DETECTION OF LIGHT STIMULUS | 96 | -0.45 | -1.74 | 0.004 | 0.542 | 0.989 | 5485 | tags=43%, list=27%, signal=58% | |
29 | SPINAL CORD DEVELOPMENT | 70 | -0.47 | -1.73 | 0.004 | 0.577 | 0.992 | 6996 | tags=50%, list=34%, signal=75% | |
30 | ACID SECRETION | 38 | -0.52 | -1.73 | 0.004 | 0.559 | 0.992 | 3494 | tags=50%, list=17%, signal=60% | |
31 | DIGESTION | 63 | -0.50 | -1.73 | 0.004 | 0.548 | 0.993 | 5139 | tags=49%, list=25%, signal=65% | |
32 | POSITIVE REGULATION OF PROTEIN KINASE A SIGNALING | 5 | -0.87 | -1.73 | 0.004 | 0.548 | 0.994 | 658 | tags=40%, list=3%, signal=41% | |
33 | LATERAL MESODERM DEVELOPMENT | 12 | -0.67 | -1.73 | 0.014 | 0.533 | 0.994 | 4600 | tags=75%, list=22%, signal=96% | |
34 | NEUTRAL LIPID CATABOLIC PROCESS | 24 | -0.58 | -1.73 | 0.012 | 0.530 | 0.994 | 4193 | tags=50%, list=20%, signal=63% | |
35 | ACYLGLYCEROL CATABOLIC PROCESS | 24 | -0.58 | -1.73 | 0.012 | 0.515 | 0.994 | 4193 | tags=50%, list=20%, signal=63% | |
36 | CYCLIC NUCLEOTIDE METABOLIC PROCESS | 39 | -0.48 | -1.72 | 0.012 | 0.532 | 0.996 | 4672 | tags=38%, list=23%, signal=50% | |
37 | POSITIVE REGULATION OF CAMP METABOLIC PROCESS | 56 | -0.48 | -1.71 | 0.004 | 0.581 | 0.998 | 5931 | tags=52%, list=29%, signal=73% | |
38 | DETECTION OF VISIBLE LIGHT | 91 | -0.45 | -1.71 | 0.004 | 0.567 | 0.998 | 5485 | tags=42%, list=27%, signal=57% | |
39 | NEGATIVE REGULATION OF VASCULAR PERMEABILITY | 7 | -0.79 | -1.71 | 0.008 | 0.566 | 0.998 | 2004 | tags=57%, list=10%, signal=63% | |
40 | ASPARTATE TRANSPORT | 6 | -0.78 | -1.71 | 0.008 | 0.557 | 0.998 | 1864 | tags=67%, list=9%, signal=73% | |
41 | LUTEINIZATION | 10 | -0.65 | -1.70 | 0.008 | 0.559 | 0.998 | 644 | tags=40%, list=3%, signal=41% | |
42 | DETECTION OF EXTERNAL STIMULUS | 110 | -0.43 | -1.70 | 0.004 | 0.547 | 0.998 | 5485 | tags=42%, list=27%, signal=57% | |
43 | REGULATION OF SMOOTHENED SIGNALING PATHWAY | 28 | -0.54 | -1.70 | 0.004 | 0.568 | 0.998 | 6071 | tags=54%, list=29%, signal=76% | |
44 | C4-DICARBOXYLATE TRANSPORT | 7 | -0.74 | -1.70 | 0.008 | 0.560 | 0.998 | 1864 | tags=57%, list=9%, signal=63% | |
45 | POSITIVE CHEMOTAXIS | 28 | -0.51 | -1.69 | 0.006 | 0.568 | 0.999 | 5854 | tags=54%, list=28%, signal=75% | |
46 | POSITIVE REGULATION OF CARTILAGE DEVELOPMENT | 13 | -0.66 | -1.69 | 0.014 | 0.560 | 0.999 | 3245 | tags=62%, list=16%, signal=73% | |
47 | EXTRACELLULAR MATRIX ASSEMBLY | 12 | -0.66 | -1.69 | 0.010 | 0.555 | 0.999 | 5860 | tags=50%, list=28%, signal=70% | |
48 | CD4-POSITIVE OR CD8-POSITIVE, ALPHA-BETA T CELL LINEAGE COMMITMENT | 10 | -0.71 | -1.69 | 0.002 | 0.549 | 0.999 | 3046 | tags=50%, list=15%, signal=59% | |
49 | NEGATIVE REGULATION OF NOTCH SIGNALING PATHWAY | 13 | -0.65 | -1.69 | 0.010 | 0.560 | 0.999 | 3982 | tags=54%, list=19%, signal=67% | |
50 | REGULATION OF NUCLEOTIDE BIOSYNTHETIC PROCESS | 83 | -0.47 | -1.69 | 0.002 | 0.558 | 1.000 | 5416 | tags=48%, list=26%, signal=65% | |
51 | REGULATION OF PURINE NUCLEOTIDE BIOSYNTHETIC PROCESS | 83 | -0.47 | -1.69 | 0.002 | 0.547 | 1.000 | 5416 | tags=48%, list=26%, signal=65% | |
52 | REGULATION OF VASCULAR PERMEABILITY | 15 | -0.63 | -1.68 | 0.014 | 0.576 | 1.000 | 2964 | tags=47%, list=14%, signal=54% | |
53 | CD4-POSITIVE, ALPHA-BETA T CELL LINEAGE COMMITMENT | 8 | -0.77 | -1.68 | 0.004 | 0.568 | 1.000 | 3046 | tags=50%, list=15%, signal=59% | |
54 | NEURON RECOGNITION | 29 | -0.53 | -1.68 | 0.009 | 0.569 | 1.000 | 2307 | tags=38%, list=11%, signal=43% | |
55 | REGULATION OF CYCLIC NUCLEOTIDE BIOSYNTHETIC PROCESS | 79 | -0.48 | -1.67 | 0.011 | 0.570 | 1.000 | 5416 | tags=48%, list=26%, signal=65% | |
56 | GLYCEROLIPID CATABOLIC PROCESS | 29 | -0.51 | -1.67 | 0.012 | 0.569 | 1.000 | 4193 | tags=45%, list=20%, signal=56% | |
57 | PROLINE METABOLIC PROCESS | 7 | -0.75 | -1.67 | 0.018 | 0.569 | 1.000 | 5066 | tags=100%, list=25%, signal=133% | |
58 | GLUTAMATE SECRETION | 24 | -0.56 | -1.67 | 0.014 | 0.567 | 1.000 | 3178 | tags=54%, list=15%, signal=64% | |
59 | PROSTATE GLAND EPITHELIUM MORPHOGENESIS | 27 | -0.52 | -1.67 | 0.020 | 0.565 | 1.000 | 4914 | tags=56%, list=24%, signal=73% | |
60 | EMBRYONIC DIGESTIVE TRACT DEVELOPMENT | 31 | -0.51 | -1.66 | 0.014 | 0.581 | 1.000 | 3815 | tags=42%, list=19%, signal=51% | |
61 | ANGIOTENSIN-ACTIVATED SIGNALING PATHWAY | 10 | -0.64 | -1.66 | 0.026 | 0.581 | 1.000 | 4012 | tags=50%, list=19%, signal=62% | |
62 | CELL DIFFERENTIATION IN SPINAL CORD | 44 | -0.49 | -1.66 | 0.012 | 0.574 | 1.000 | 6996 | tags=50%, list=34%, signal=76% | |
63 | NEGATIVE REGULATION OF CHONDROCYTE DIFFERENTIATION | 10 | -0.69 | -1.66 | 0.020 | 0.571 | 1.000 | 3245 | tags=60%, list=16%, signal=71% | |
64 | NEGATIVE REGULATION OF CARTILAGE DEVELOPMENT | 10 | -0.69 | -1.66 | 0.020 | 0.562 | 1.000 | 3245 | tags=60%, list=16%, signal=71% | |
65 | EMBRYONIC DIGESTIVE TRACT MORPHOGENESIS | 17 | -0.58 | -1.66 | 0.027 | 0.556 | 1.000 | 3815 | tags=47%, list=19%, signal=58% | |
66 | POSITIVE REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 12 | -0.66 | -1.66 | 0.021 | 0.547 | 1.000 | 160 | tags=25%, list=1%, signal=25% | |
67 | PROTEIN KINASE C SIGNALING | 12 | -0.69 | -1.66 | 0.016 | 0.543 | 1.000 | 2786 | tags=42%, list=14%, signal=48% | |
68 | SKELETAL MUSCLE TISSUE DEVELOPMENT | 114 | -0.40 | -1.66 | 0.000 | 0.542 | 1.000 | 4148 | tags=36%, list=20%, signal=45% | |
69 | POSITIVE REGULATION OF POSTTRANSCRIPTIONAL GENE SILENCING | 5 | -0.75 | -1.66 | 0.014 | 0.539 | 1.000 | 1097 | tags=40%, list=5%, signal=42% | |
70 | NEGATIVE REGULATION OF SMOOTHENED SIGNALING PATHWAY | 14 | -0.62 | -1.66 | 0.022 | 0.536 | 1.000 | 5657 | tags=57%, list=27%, signal=79% | |
71 | REGULATION OF HIPPO SIGNALING | 8 | -0.71 | -1.66 | 0.008 | 0.535 | 1.000 | 2100 | tags=50%, list=10%, signal=56% | |
72 | DETECTION OF ABIOTIC STIMULUS | 114 | -0.41 | -1.65 | 0.006 | 0.543 | 1.000 | 5485 | tags=40%, list=27%, signal=55% | |
73 | PROSTATE GLAND MORPHOGENESIS | 29 | -0.51 | -1.65 | 0.016 | 0.543 | 1.000 | 4914 | tags=52%, list=24%, signal=68% | |
74 | VENTRAL SPINAL CORD DEVELOPMENT | 37 | -0.48 | -1.65 | 0.018 | 0.537 | 1.000 | 6996 | tags=51%, list=34%, signal=78% | |
75 | ASPARTATE METABOLIC PROCESS | 5 | -0.80 | -1.65 | 0.014 | 0.537 | 1.000 | 2159 | tags=40%, list=10%, signal=45% | |
76 | REGULATION OF NATURAL KILLER CELL CHEMOTAXIS | 6 | -0.88 | -1.65 | 0.002 | 0.533 | 1.000 | 26 | tags=33%, list=0%, signal=33% | |
77 | POSITIVE REGULATION OF CYCLASE ACTIVITY | 35 | -0.51 | -1.65 | 0.023 | 0.534 | 1.000 | 4575 | tags=51%, list=22%, signal=66% | |
78 | RHODOPSIN MEDIATED SIGNALING PATHWAY | 32 | -0.48 | -1.65 | 0.025 | 0.528 | 1.000 | 4833 | tags=41%, list=23%, signal=53% | |
79 | SKELETAL MUSCLE ORGAN DEVELOPMENT | 123 | -0.40 | -1.64 | 0.002 | 0.534 | 1.000 | 4148 | tags=36%, list=20%, signal=45% | |
80 | POSITIVE REGULATION OF PURINE NUCLEOTIDE METABOLIC PROCESS | 79 | -0.44 | -1.64 | 0.006 | 0.554 | 1.000 | 5416 | tags=47%, list=26%, signal=63% | |
81 | REGULATION OF CAMP BIOSYNTHETIC PROCESS | 71 | -0.46 | -1.64 | 0.015 | 0.557 | 1.000 | 5416 | tags=46%, list=26%, signal=63% | |
82 | METANEPHRIC NEPHRON MORPHOGENESIS | 16 | -0.58 | -1.64 | 0.014 | 0.559 | 1.000 | 3327 | tags=50%, list=16%, signal=60% | |
83 | ACROSOME REACTION | 7 | -0.71 | -1.64 | 0.012 | 0.559 | 1.000 | 4115 | tags=71%, list=20%, signal=89% | |
84 | REGULATION OF MACROPHAGE CYTOKINE PRODUCTION | 9 | -0.70 | -1.63 | 0.018 | 0.553 | 1.000 | 3534 | tags=44%, list=17%, signal=54% | |
85 | REGULATION OF RHODOPSIN MEDIATED SIGNALING PATHWAY | 31 | -0.49 | -1.63 | 0.033 | 0.548 | 1.000 | 4833 | tags=42%, list=23%, signal=55% | |
86 | POSITIVE REGULATION OF NUCLEOTIDE METABOLIC PROCESS | 80 | -0.44 | -1.63 | 0.006 | 0.544 | 1.000 | 5416 | tags=46%, list=26%, signal=62% | |
87 | REGULATION OF GUANYLATE CYCLASE ACTIVITY | 6 | -0.78 | -1.63 | 0.020 | 0.541 | 1.000 | 4575 | tags=83%, list=22%, signal=107% | |
88 | MESODERMAL CELL DIFFERENTIATION | 23 | -0.55 | -1.63 | 0.024 | 0.540 | 1.000 | 4380 | tags=48%, list=21%, signal=61% | |
89 | ALPHA-BETA T CELL LINEAGE COMMITMENT | 10 | -0.67 | -1.63 | 0.020 | 0.544 | 1.000 | 3046 | tags=40%, list=15%, signal=47% | |
90 | POSITIVE REGULATION OF NON-CANONICAL WNT SIGNALING PATHWAY | 6 | -0.73 | -1.63 | 0.012 | 0.546 | 1.000 | 523 | tags=33%, list=3%, signal=34% | |
91 | GABAERGIC NEURON DIFFERENTIATION | 13 | -0.69 | -1.62 | 0.025 | 0.572 | 1.000 | 743 | tags=38%, list=4%, signal=40% | |
92 | HINDGUT DEVELOPMENT | 7 | -0.69 | -1.62 | 0.029 | 0.568 | 1.000 | 3650 | tags=57%, list=18%, signal=69% | |
93 | CAMP METABOLIC PROCESS | 25 | -0.50 | -1.62 | 0.028 | 0.565 | 1.000 | 4570 | tags=40%, list=22%, signal=51% | |
94 | NEGATIVE REGULATION OF HIPPO SIGNALING | 5 | -0.83 | -1.62 | 0.006 | 0.566 | 1.000 | 2100 | tags=80%, list=10%, signal=89% | |
95 | REGULATION OF GENE SILENCING BY MIRNA | 7 | -0.68 | -1.62 | 0.041 | 0.570 | 1.000 | 1097 | tags=29%, list=5%, signal=30% | |
96 | POSITIVE REGULATION OF BRANCHING INVOLVED IN URETERIC BUD MORPHOGENESIS | 11 | -0.64 | -1.62 | 0.021 | 0.578 | 1.000 | 6755 | tags=82%, list=33%, signal=122% | |
97 | CELL-CELL JUNCTION ASSEMBLY | 62 | -0.43 | -1.61 | 0.014 | 0.578 | 1.000 | 3445 | tags=35%, list=17%, signal=42% | |
98 | REGULATION OF ASTROCYTE DIFFERENTIATION | 23 | -0.53 | -1.61 | 0.031 | 0.577 | 1.000 | 5282 | tags=48%, list=26%, signal=64% | |
99 | REGULATION OF IMMATURE T CELL PROLIFERATION | 5 | -0.81 | -1.61 | 0.008 | 0.576 | 1.000 | 2803 | tags=60%, list=14%, signal=69% | |
100 | REGULATION OF IMMATURE T CELL PROLIFERATION IN THYMUS | 5 | -0.81 | -1.61 | 0.008 | 0.570 | 1.000 | 2803 | tags=60%, list=14%, signal=69% | |
101 | REGULATION OF MESENCHYMAL STEM CELL DIFFERENTIATION | 6 | -0.73 | -1.61 | 0.014 | 0.565 | 1.000 | 4909 | tags=83%, list=24%, signal=109% | |
102 | REGULATION OF CELL CHEMOTAXIS TO FIBROBLAST GROWTH FACTOR | 7 | -0.71 | -1.61 | 0.016 | 0.563 | 1.000 | 4835 | tags=71%, list=23%, signal=93% | |
103 | REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS TO FIBROBLAST GROWTH FACTOR | 7 | -0.71 | -1.61 | 0.016 | 0.557 | 1.000 | 4835 | tags=71%, list=23%, signal=93% | |
104 | CYCLIC NUCLEOTIDE BIOSYNTHETIC PROCESS | 27 | -0.51 | -1.61 | 0.032 | 0.555 | 1.000 | 4407 | tags=41%, list=21%, signal=52% | |
105 | CYCLIC PURINE NUCLEOTIDE METABOLIC PROCESS | 27 | -0.51 | -1.61 | 0.032 | 0.549 | 1.000 | 4407 | tags=41%, list=21%, signal=52% | |
106 | POSITIVE REGULATION OF KIDNEY DEVELOPMENT | 29 | -0.51 | -1.61 | 0.022 | 0.568 | 1.000 | 6755 | tags=69%, list=33%, signal=102% | |
107 | POSITIVE REGULATION OF CYCLIC NUCLEOTIDE METABOLIC PROCESS | 66 | -0.46 | -1.60 | 0.016 | 0.587 | 1.000 | 5416 | tags=47%, list=26%, signal=64% | |
108 | NERVE DEVELOPMENT | 66 | -0.41 | -1.60 | 0.014 | 0.592 | 1.000 | 5279 | tags=42%, list=26%, signal=57% | |
109 | REGULATION OF LYASE ACTIVITY | 52 | -0.46 | -1.60 | 0.025 | 0.598 | 1.000 | 4147 | tags=44%, list=20%, signal=55% | |
110 | REGULATION OF T CELL APOPTOTIC PROCESS | 15 | -0.60 | -1.59 | 0.016 | 0.608 | 1.000 | 2133 | tags=27%, list=10%, signal=30% | |
111 | POSITIVE REGULATION OF STEM CELL DIFFERENTIATION | 38 | -0.43 | -1.59 | 0.010 | 0.628 | 1.000 | 3238 | tags=26%, list=16%, signal=31% | |
112 | POSITIVE REGULATION OF STRESS FIBER ASSEMBLY | 27 | -0.49 | -1.59 | 0.014 | 0.624 | 1.000 | 2524 | tags=37%, list=12%, signal=42% | |
113 | REGULATION OF ADENYLATE CYCLASE ACTIVITY | 42 | -0.48 | -1.59 | 0.027 | 0.621 | 1.000 | 3717 | tags=43%, list=18%, signal=52% | |
114 | REGULATION OF DNA METHYLATION | 5 | -0.76 | -1.59 | 0.019 | 0.630 | 1.000 | 2211 | tags=40%, list=11%, signal=45% | |
115 | ACIDIC AMINO ACID TRANSPORT | 12 | -0.59 | -1.58 | 0.024 | 0.632 | 1.000 | 1864 | tags=42%, list=9%, signal=46% | |
116 | L-GLUTAMATE TRANSPORT | 12 | -0.59 | -1.58 | 0.024 | 0.627 | 1.000 | 1864 | tags=42%, list=9%, signal=46% | |
117 | CELL MIGRATION INVOLVED IN GASTRULATION | 16 | -0.56 | -1.58 | 0.028 | 0.630 | 1.000 | 7323 | tags=75%, list=36%, signal=116% | |
118 | AXIS ELONGATION | 26 | -0.51 | -1.58 | 0.033 | 0.628 | 1.000 | 3951 | tags=46%, list=19%, signal=57% | |
119 | L-AMINO ACID IMPORT | 5 | -0.82 | -1.58 | 0.018 | 0.634 | 1.000 | 1864 | tags=60%, list=9%, signal=66% | |
120 | METANEPHRIC NEPHRON TUBULE MORPHOGENESIS | 6 | -0.76 | -1.58 | 0.021 | 0.634 | 1.000 | 2935 | tags=67%, list=14%, signal=78% | |
121 | REGULATION OF HEART MORPHOGENESIS | 13 | -0.61 | -1.58 | 0.033 | 0.633 | 1.000 | 5430 | tags=62%, list=26%, signal=84% | |
122 | BRANCH ELONGATION OF AN EPITHELIUM | 17 | -0.53 | -1.58 | 0.034 | 0.634 | 1.000 | 3951 | tags=47%, list=19%, signal=58% | |
123 | REGULATION OF INOSITOL PHOSPHATE BIOSYNTHETIC PROCESS | 6 | -0.75 | -1.58 | 0.022 | 0.638 | 1.000 | 4047 | tags=67%, list=20%, signal=83% | |
124 | METANEPHROS MORPHOGENESIS | 21 | -0.52 | -1.58 | 0.024 | 0.633 | 1.000 | 6755 | tags=62%, list=33%, signal=92% | |
125 | CILIUM MOVEMENT | 13 | -0.59 | -1.58 | 0.030 | 0.630 | 1.000 | 5901 | tags=62%, list=29%, signal=86% | |
126 | REGULATION OF STEM CELL DIFFERENTIATION | 81 | -0.37 | -1.57 | 0.010 | 0.633 | 1.000 | 4336 | tags=31%, list=21%, signal=39% | |
127 | SPINAL CORD MOTOR NEURON DIFFERENTIATION | 30 | -0.47 | -1.57 | 0.024 | 0.632 | 1.000 | 3650 | tags=30%, list=18%, signal=36% | |
128 | POSITIVE REGULATION OF ACTIN FILAMENT BUNDLE ASSEMBLY | 31 | -0.47 | -1.57 | 0.017 | 0.630 | 1.000 | 2524 | tags=32%, list=12%, signal=37% | |
129 | REGULATION OF GLYCOGEN BIOSYNTHETIC PROCESS | 18 | -0.55 | -1.57 | 0.038 | 0.635 | 1.000 | 4049 | tags=44%, list=20%, signal=55% | |
130 | REGULATION OF GLUCAN BIOSYNTHETIC PROCESS | 18 | -0.55 | -1.57 | 0.038 | 0.630 | 1.000 | 4049 | tags=44%, list=20%, signal=55% | |
131 | FACIAL NERVE DEVELOPMENT | 10 | -0.67 | -1.57 | 0.031 | 0.625 | 1.000 | 4337 | tags=60%, list=21%, signal=76% | |
132 | FACIAL NERVE MORPHOGENESIS | 10 | -0.67 | -1.57 | 0.031 | 0.621 | 1.000 | 4337 | tags=60%, list=21%, signal=76% | |
133 | NUCLEOSIDE TRANSPORT | 9 | -0.64 | -1.57 | 0.038 | 0.626 | 1.000 | 2209 | tags=44%, list=11%, signal=50% | |
134 | NUCLEOSIDE TRANSMEMBRANE TRANSPORT | 9 | -0.64 | -1.57 | 0.038 | 0.621 | 1.000 | 2209 | tags=44%, list=11%, signal=50% | |
135 | NEGATIVE REGULATION OF MACROPHAGE CYTOKINE PRODUCTION | 5 | -0.79 | -1.57 | 0.014 | 0.617 | 1.000 | 2471 | tags=40%, list=12%, signal=45% | |
136 | REGULATION OF RECEPTOR RECYCLING | 11 | -0.56 | -1.57 | 0.022 | 0.617 | 1.000 | 4352 | tags=64%, list=21%, signal=81% | |
137 | BICARBONATE TRANSPORT | 31 | -0.51 | -1.57 | 0.038 | 0.614 | 1.000 | 5372 | tags=52%, list=26%, signal=70% | |
138 | METANEPHRIC RENAL VESICLE MORPHOGENESIS | 9 | -0.65 | -1.57 | 0.037 | 0.611 | 1.000 | 3327 | tags=56%, list=16%, signal=66% | |
139 | BICELLULAR TIGHT JUNCTION ASSEMBLY | 30 | -0.49 | -1.57 | 0.030 | 0.611 | 1.000 | 3445 | tags=40%, list=17%, signal=48% | |
140 | CELLULAR RESPONSE TO PROSTAGLANDIN STIMULUS | 10 | -0.67 | -1.56 | 0.058 | 0.635 | 1.000 | 3350 | tags=50%, list=16%, signal=60% | |
141 | REGULATION OF CELL PROLIFERATION INVOLVED IN HEART MORPHOGENESIS | 7 | -0.66 | -1.56 | 0.030 | 0.635 | 1.000 | 1523 | tags=43%, list=7%, signal=46% | |
142 | EPIBOLY | 18 | -0.52 | -1.56 | 0.026 | 0.640 | 1.000 | 3159 | tags=39%, list=15%, signal=46% | |
143 | NEGATIVE REGULATION OF CYTOKINE BIOSYNTHETIC PROCESS | 16 | -0.58 | -1.56 | 0.024 | 0.637 | 1.000 | 2592 | tags=38%, list=13%, signal=43% | |
144 | REGULATION OF ORGAN FORMATION | 26 | -0.51 | -1.56 | 0.043 | 0.642 | 1.000 | 4215 | tags=42%, list=20%, signal=53% | |
145 | REGULATION OF ORGAN MORPHOGENESIS | 93 | -0.39 | -1.55 | 0.012 | 0.649 | 1.000 | 5743 | tags=47%, list=28%, signal=65% | |
146 | RENAL VESICLE MORPHOGENESIS | 12 | -0.58 | -1.55 | 0.038 | 0.645 | 1.000 | 6755 | tags=67%, list=33%, signal=99% | |
147 | POSITIVE REGULATION OF GLYCOGEN BIOSYNTHETIC PROCESS | 12 | -0.56 | -1.55 | 0.043 | 0.641 | 1.000 | 4049 | tags=42%, list=20%, signal=52% | |
148 | NEGATIVE REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 15 | -0.56 | -1.55 | 0.026 | 0.643 | 1.000 | 4281 | tags=53%, list=21%, signal=67% | |
149 | ESTABLISHMENT OF EPITHELIAL CELL POLARITY | 12 | -0.57 | -1.55 | 0.056 | 0.641 | 1.000 | 3692 | tags=42%, list=18%, signal=51% | |
150 | REGULATION OF POSITIVE CHEMOTAXIS | 12 | -0.57 | -1.55 | 0.042 | 0.646 | 1.000 | 2822 | tags=50%, list=14%, signal=58% | |
151 | ECTODERMAL PLACODE FORMATION | 15 | -0.55 | -1.55 | 0.051 | 0.645 | 1.000 | 6442 | tags=67%, list=31%, signal=97% | |
152 | ECTODERMAL PLACODE DEVELOPMENT | 15 | -0.55 | -1.55 | 0.051 | 0.641 | 1.000 | 6442 | tags=67%, list=31%, signal=97% | |
153 | ECTODERMAL PLACODE MORPHOGENESIS | 15 | -0.55 | -1.55 | 0.051 | 0.636 | 1.000 | 6442 | tags=67%, list=31%, signal=97% | |
154 | PERIPHERAL NERVOUS SYSTEM DEVELOPMENT | 67 | -0.41 | -1.55 | 0.010 | 0.639 | 1.000 | 3793 | tags=31%, list=18%, signal=38% | |
155 | HEPOXILIN METABOLIC PROCESS | 5 | -0.79 | -1.55 | 0.027 | 0.640 | 1.000 | 683 | tags=40%, list=3%, signal=41% | |
156 | HEPOXILIN BIOSYNTHETIC PROCESS | 5 | -0.79 | -1.55 | 0.027 | 0.636 | 1.000 | 683 | tags=40%, list=3%, signal=41% | |
157 | INDUCTION OF POSITIVE CHEMOTAXIS | 6 | -0.74 | -1.55 | 0.021 | 0.636 | 1.000 | 1312 | tags=50%, list=6%, signal=53% | |
158 | PEPTIDYL-HISTIDINE MODIFICATION | 5 | -0.70 | -1.55 | 0.036 | 0.636 | 1.000 | 2040 | tags=40%, list=10%, signal=44% | |
159 | UTERUS DEVELOPMENT | 21 | -0.49 | -1.55 | 0.029 | 0.632 | 1.000 | 5437 | tags=52%, list=26%, signal=71% | |
160 | MYELINATION IN PERIPHERAL NERVOUS SYSTEM | 20 | -0.47 | -1.54 | 0.027 | 0.635 | 1.000 | 4820 | tags=35%, list=23%, signal=46% | |
161 | PERIPHERAL NERVOUS SYSTEM AXON ENSHEATHMENT | 20 | -0.47 | -1.54 | 0.027 | 0.631 | 1.000 | 4820 | tags=35%, list=23%, signal=46% | |
162 | CELL MIGRATION INVOLVED IN SPROUTING ANGIOGENESIS | 13 | -0.58 | -1.54 | 0.031 | 0.634 | 1.000 | 2119 | tags=31%, list=10%, signal=34% | |
163 | POSITIVE REGULATION OF KERATINOCYTE PROLIFERATION | 7 | -0.74 | -1.54 | 0.030 | 0.632 | 1.000 | 3815 | tags=57%, list=19%, signal=70% | |
164 | NEGATIVE REGULATION OF PROTEIN OLIGOMERIZATION | 9 | -0.62 | -1.54 | 0.035 | 0.634 | 1.000 | 1531 | tags=33%, list=7%, signal=36% | |
165 | REGULATION OF PLATELET-DERIVED GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 11 | -0.59 | -1.54 | 0.046 | 0.631 | 1.000 | 2822 | tags=36%, list=14%, signal=42% | |
166 | T-HELPER CELL LINEAGE COMMITMENT | 7 | -0.75 | -1.54 | 0.025 | 0.627 | 1.000 | 3046 | tags=43%, list=15%, signal=50% | |
167 | REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 52 | -0.39 | -1.54 | 0.016 | 0.623 | 1.000 | 4336 | tags=31%, list=21%, signal=39% | |
168 | REGULATION OF CHOLESTEROL METABOLIC PROCESS | 8 | -0.64 | -1.54 | 0.049 | 0.622 | 1.000 | 2857 | tags=38%, list=14%, signal=44% | |
169 | MALE SEX DETERMINATION | 13 | -0.56 | -1.54 | 0.051 | 0.620 | 1.000 | 6460 | tags=69%, list=31%, signal=101% | |
170 | NOTOCHORD MORPHOGENESIS | 10 | -0.61 | -1.54 | 0.049 | 0.629 | 1.000 | 6710 | tags=80%, list=33%, signal=119% | |
171 | POSITIVE REGULATION OF STEROID METABOLIC PROCESS | 15 | -0.56 | -1.54 | 0.058 | 0.633 | 1.000 | 5414 | tags=53%, list=26%, signal=72% | |
172 | POSITIVE REGULATION OF GUANYLATE CYCLASE ACTIVITY | 5 | -0.77 | -1.54 | 0.034 | 0.629 | 1.000 | 4575 | tags=80%, list=22%, signal=103% | |
173 | NEGATIVE REGULATION OF ANDROGEN RECEPTOR SIGNALING PATHWAY | 12 | -0.55 | -1.54 | 0.035 | 0.631 | 1.000 | 4506 | tags=50%, list=22%, signal=64% | |
174 | NEGATIVE REGULATION OF EPIDERMIS DEVELOPMENT | 10 | -0.63 | -1.53 | 0.033 | 0.633 | 1.000 | 2781 | tags=50%, list=13%, signal=58% | |
175 | CELL MATURATION | 112 | -0.36 | -1.53 | 0.008 | 0.632 | 1.000 | 5743 | tags=44%, list=28%, signal=60% | |
176 | ENDOCRINE PROCESS | 28 | -0.51 | -1.53 | 0.040 | 0.636 | 1.000 | 3574 | tags=43%, list=17%, signal=52% | |
177 | EMBRYO IMPLANTATION | 33 | -0.46 | -1.53 | 0.014 | 0.632 | 1.000 | 5528 | tags=48%, list=27%, signal=66% | |
178 | REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE MEDIATED BY A CHEMICAL SIGNAL | 26 | -0.52 | -1.53 | 0.037 | 0.630 | 1.000 | 3574 | tags=42%, list=17%, signal=51% | |
179 | PERIPHERAL NERVOUS SYSTEM NEURON DIFFERENTIATION | 13 | -0.54 | -1.53 | 0.036 | 0.627 | 1.000 | 2243 | tags=31%, list=11%, signal=35% | |
180 | PERIPHERAL NERVOUS SYSTEM NEURON DEVELOPMENT | 13 | -0.54 | -1.53 | 0.036 | 0.623 | 1.000 | 2243 | tags=31%, list=11%, signal=35% | |
181 | REGULATION OF ANDROGEN RECEPTOR SIGNALING PATHWAY | 22 | -0.51 | -1.53 | 0.047 | 0.622 | 1.000 | 4506 | tags=50%, list=22%, signal=64% | |
182 | POSITIVE REGULATION OF CALCIUM ION-DEPENDENT EXOCYTOSIS | 12 | -0.58 | -1.53 | 0.061 | 0.630 | 1.000 | 3091 | tags=50%, list=15%, signal=59% | |
183 | CELL JUNCTION ASSEMBLY | 131 | -0.38 | -1.53 | 0.020 | 0.629 | 1.000 | 4853 | tags=37%, list=24%, signal=49% | |
184 | PARASYMPATHETIC NERVOUS SYSTEM DEVELOPMENT | 17 | -0.56 | -1.53 | 0.048 | 0.627 | 1.000 | 6400 | tags=59%, list=31%, signal=85% | |
185 | CAMP BIOSYNTHETIC PROCESS | 16 | -0.51 | -1.53 | 0.040 | 0.626 | 1.000 | 4407 | tags=44%, list=21%, signal=56% | |
186 | AUTONOMIC NERVOUS SYSTEM DEVELOPMENT | 39 | -0.46 | -1.53 | 0.034 | 0.628 | 1.000 | 6720 | tags=51%, list=33%, signal=76% | |
187 | EYE PIGMENTATION | 7 | -0.64 | -1.52 | 0.031 | 0.636 | 1.000 | 7208 | tags=86%, list=35%, signal=132% | |
188 | NEGATIVE REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 8 | -0.61 | -1.52 | 0.046 | 0.635 | 1.000 | 1246 | tags=25%, list=6%, signal=27% | |
189 | REGULATION OF CAMP METABOLIC PROCESS | 80 | -0.41 | -1.52 | 0.031 | 0.639 | 1.000 | 5416 | tags=44%, list=26%, signal=59% | |
190 | VENTRAL MIDLINE DEVELOPMENT | 5 | -0.74 | -1.52 | 0.045 | 0.648 | 1.000 | 3327 | tags=80%, list=16%, signal=95% | |
191 | HINDBRAIN MORPHOGENESIS | 44 | -0.42 | -1.52 | 0.037 | 0.647 | 1.000 | 6120 | tags=43%, list=30%, signal=61% | |
192 | MUSCLE ORGAN DEVELOPMENT | 232 | -0.36 | -1.52 | 0.006 | 0.646 | 1.000 | 4298 | tags=34%, list=21%, signal=43% | |
193 | NEGATIVE REGULATION OF STEROL TRANSPORT | 10 | -0.69 | -1.52 | 0.040 | 0.646 | 1.000 | 5596 | tags=90%, list=27%, signal=123% | |
194 | NEGATIVE REGULATION OF CHOLESTEROL TRANSPORT | 10 | -0.69 | -1.52 | 0.040 | 0.643 | 1.000 | 5596 | tags=90%, list=27%, signal=123% | |
195 | RENAL VESICLE FORMATION | 6 | -0.68 | -1.52 | 0.048 | 0.647 | 1.000 | 5050 | tags=67%, list=25%, signal=88% | |
196 | CEREBELLUM MORPHOGENESIS | 42 | -0.42 | -1.52 | 0.046 | 0.648 | 1.000 | 6120 | tags=43%, list=30%, signal=61% | |
197 | METANEPHRIC TUBULE MORPHOGENESIS | 8 | -0.67 | -1.51 | 0.064 | 0.653 | 1.000 | 6755 | tags=88%, list=33%, signal=130% | |
198 | VENTRAL SPINAL CORD INTERNEURON DIFFERENTIATION | 16 | -0.59 | -1.51 | 0.045 | 0.653 | 1.000 | 1212 | tags=25%, list=6%, signal=27% | |
199 | MYOFIBRIL ASSEMBLY | 40 | -0.42 | -1.51 | 0.041 | 0.660 | 1.000 | 4823 | tags=38%, list=23%, signal=49% | |
200 | RHOMBOMERE DEVELOPMENT | 8 | -0.69 | -1.51 | 0.054 | 0.662 | 1.000 | 2293 | tags=50%, list=11%, signal=56% | |
201 | DIGESTIVE SYSTEM DEVELOPMENT | 115 | -0.36 | -1.51 | 0.008 | 0.659 | 1.000 | 7048 | tags=51%, list=34%, signal=78% | |
202 | RESPONSE TO PROSTAGLANDIN | 13 | -0.60 | -1.51 | 0.089 | 0.658 | 1.000 | 5951 | tags=62%, list=29%, signal=86% | |
203 | SEMICIRCULAR CANAL DEVELOPMENT | 9 | -0.63 | -1.51 | 0.053 | 0.665 | 1.000 | 4380 | tags=56%, list=21%, signal=71% | |
204 | CELLULAR RESPONSE TO RETINOIC ACID | 34 | -0.45 | -1.51 | 0.047 | 0.663 | 1.000 | 4076 | tags=44%, list=20%, signal=55% | |
205 | DORSAL/VENTRAL PATTERN FORMATION | 83 | -0.41 | -1.50 | 0.039 | 0.677 | 1.000 | 6352 | tags=46%, list=31%, signal=66% | |
206 | ACYLGLYCEROL HOMEOSTASIS | 20 | -0.53 | -1.50 | 0.045 | 0.678 | 1.000 | 4193 | tags=45%, list=20%, signal=56% | |
207 | TRIGLYCERIDE HOMEOSTASIS | 20 | -0.53 | -1.50 | 0.045 | 0.675 | 1.000 | 4193 | tags=45%, list=20%, signal=56% | |
208 | ANTERIOR/POSTERIOR PATTERN SPECIFICATION | 185 | -0.35 | -1.50 | 0.015 | 0.687 | 1.000 | 3985 | tags=31%, list=19%, signal=38% | |
209 | ACTOMYOSIN STRUCTURE ORGANIZATION | 57 | -0.38 | -1.50 | 0.026 | 0.686 | 1.000 | 3896 | tags=28%, list=19%, signal=35% | |
210 | REGULATION OF ACTIN FILAMENT BUNDLE ASSEMBLY | 50 | -0.39 | -1.50 | 0.032 | 0.685 | 1.000 | 2524 | tags=30%, list=12%, signal=34% | |
211 | FOREBRAIN VENTRICULAR ZONE PROGENITOR CELL DIVISION | 6 | -0.70 | -1.50 | 0.054 | 0.685 | 1.000 | 1609 | tags=33%, list=8%, signal=36% | |
212 | VENTRAL SPINAL CORD INTERNEURON SPECIFICATION | 10 | -0.65 | -1.50 | 0.065 | 0.688 | 1.000 | 6996 | tags=70%, list=34%, signal=106% | |
213 | CELL FATE SPECIFICATION INVOLVED IN PATTERN SPECIFICATION | 10 | -0.65 | -1.50 | 0.065 | 0.685 | 1.000 | 6996 | tags=70%, list=34%, signal=106% | |
214 | DOPAMINE METABOLIC PROCESS | 9 | -0.65 | -1.50 | 0.071 | 0.686 | 1.000 | 5066 | tags=56%, list=25%, signal=74% | |
215 | FACIAL NERVE STRUCTURAL ORGANIZATION | 9 | -0.65 | -1.50 | 0.064 | 0.684 | 1.000 | 4337 | tags=56%, list=21%, signal=70% | |
216 | SPINAL CORD PATTERNING | 25 | -0.53 | -1.50 | 0.057 | 0.681 | 1.000 | 6996 | tags=56%, list=34%, signal=85% | |
217 | INORGANIC ANION TRANSPORT | 65 | -0.41 | -1.50 | 0.032 | 0.680 | 1.000 | 3676 | tags=31%, list=18%, signal=37% | |
218 | CALCIUM-INDEPENDENT CELL-CELL ADHESION VIA PLASMA MEMBRANE CELL-ADHESION MOLECULES | 19 | -0.56 | -1.49 | 0.083 | 0.679 | 1.000 | 3445 | tags=47%, list=17%, signal=57% | |
219 | REGULATION OF SMOOTH MUSCLE CELL APOPTOTIC PROCESS | 8 | -0.61 | -1.49 | 0.068 | 0.677 | 1.000 | 1746 | tags=25%, list=8%, signal=27% | |
220 | KERATINIZATION | 10 | -0.60 | -1.49 | 0.060 | 0.682 | 1.000 | 1425 | tags=40%, list=7%, signal=43% | |
221 | TUBE LUMEN CAVITATION | 5 | -0.76 | -1.49 | 0.042 | 0.679 | 1.000 | 2803 | tags=60%, list=14%, signal=69% | |
222 | SALIVARY GLAND CAVITATION | 5 | -0.76 | -1.49 | 0.042 | 0.676 | 1.000 | 2803 | tags=60%, list=14%, signal=69% | |
223 | THYROID HORMONE GENERATION | 9 | -0.64 | -1.49 | 0.065 | 0.679 | 1.000 | 4455 | tags=44%, list=22%, signal=57% | |
224 | CEREBRAL CORTEX GABAERGIC INTERNEURON MIGRATION | 6 | -0.76 | -1.49 | 0.048 | 0.688 | 1.000 | 3494 | tags=67%, list=17%, signal=80% | |
225 | INTERNEURON MIGRATION | 6 | -0.76 | -1.49 | 0.048 | 0.685 | 1.000 | 3494 | tags=67%, list=17%, signal=80% | |
226 | CELL-CELL JUNCTION ORGANIZATION | 118 | -0.37 | -1.49 | 0.020 | 0.686 | 1.000 | 4853 | tags=36%, list=24%, signal=47% | |
227 | ASYMMETRIC CELL DIVISION | 10 | -0.58 | -1.49 | 0.048 | 0.684 | 1.000 | 2748 | tags=30%, list=13%, signal=35% | |
228 | CELL FATE SPECIFICATION | 64 | -0.45 | -1.49 | 0.076 | 0.690 | 1.000 | 3677 | tags=34%, list=18%, signal=42% | |
229 | CRANIAL NERVE STRUCTURAL ORGANIZATION | 12 | -0.59 | -1.49 | 0.057 | 0.688 | 1.000 | 7516 | tags=75%, list=36%, signal=118% | |
230 | REGULATION OF STEROID METABOLIC PROCESS | 41 | -0.41 | -1.48 | 0.036 | 0.690 | 1.000 | 5414 | tags=39%, list=26%, signal=53% | |
231 | PROSTATE GLANDULAR ACINUS MORPHOGENESIS | 7 | -0.68 | -1.48 | 0.066 | 0.687 | 1.000 | 4215 | tags=71%, list=20%, signal=90% | |
232 | PROSTATE EPITHELIAL CORD ARBORIZATION INVOLVED IN PROSTATE GLANDULAR ACINUS MORPHOGENESIS | 7 | -0.68 | -1.48 | 0.066 | 0.684 | 1.000 | 4215 | tags=71%, list=20%, signal=90% | |
233 | AXONAL FASCICULATION | 18 | -0.49 | -1.48 | 0.069 | 0.682 | 1.000 | 5282 | tags=44%, list=26%, signal=60% | |
234 | CRANIOFACIAL SUTURE MORPHOGENESIS | 13 | -0.55 | -1.48 | 0.061 | 0.680 | 1.000 | 4206 | tags=46%, list=20%, signal=58% | |
235 | GANGLIOSIDE METABOLIC PROCESS | 9 | -0.60 | -1.48 | 0.073 | 0.683 | 1.000 | 1303 | tags=44%, list=6%, signal=47% | |
236 | SPINAL CORD MOTOR NEURON CELL FATE SPECIFICATION | 12 | -0.59 | -1.48 | 0.092 | 0.681 | 1.000 | 3650 | tags=42%, list=18%, signal=51% | |
237 | CALCIUM ION TRANSPORT INTO CYTOSOL | 37 | -0.40 | -1.48 | 0.051 | 0.682 | 1.000 | 5630 | tags=43%, list=27%, signal=59% | |
238 | NEGATIVE REGULATION OF BONE REMODELING | 5 | -0.72 | -1.48 | 0.048 | 0.684 | 1.000 | 790 | tags=40%, list=4%, signal=42% | |
239 | INTEGRIN-MEDIATED SIGNALING PATHWAY | 38 | -0.46 | -1.48 | 0.057 | 0.685 | 1.000 | 4548 | tags=34%, list=22%, signal=44% | |
240 | SENSORY PERCEPTION OF SMELL | 12 | -0.54 | -1.48 | 0.072 | 0.686 | 1.000 | 7535 | tags=58%, list=37%, signal=92% | |
241 | CELL-CELL ADHESION VIA PLASMA-MEMBRANE ADHESION MOLECULES | 66 | -0.41 | -1.48 | 0.051 | 0.704 | 1.000 | 3664 | tags=33%, list=18%, signal=40% | |
242 | REGULATION OF ENDOTHELIAL CELL APOPTOTIC PROCESS | 27 | -0.47 | -1.48 | 0.050 | 0.701 | 1.000 | 4868 | tags=44%, list=24%, signal=58% | |
243 | REGULATION OF G-PROTEIN COUPLED RECEPTOR PROTEIN SIGNALING PATHWAY | 93 | -0.36 | -1.47 | 0.023 | 0.701 | 1.000 | 5825 | tags=40%, list=28%, signal=55% | |
244 | DICARBOXYLIC ACID TRANSPORT | 43 | -0.42 | -1.47 | 0.049 | 0.701 | 1.000 | 3178 | tags=35%, list=15%, signal=41% | |
245 | POLYKETIDE METABOLIC PROCESS | 8 | -0.68 | -1.47 | 0.082 | 0.701 | 1.000 | 2655 | tags=50%, list=13%, signal=57% | |
246 | AMINOGLYCOSIDE ANTIBIOTIC METABOLIC PROCESS | 8 | -0.68 | -1.47 | 0.082 | 0.698 | 1.000 | 2655 | tags=50%, list=13%, signal=57% | |
247 | DAUNORUBICIN METABOLIC PROCESS | 8 | -0.68 | -1.47 | 0.082 | 0.695 | 1.000 | 2655 | tags=50%, list=13%, signal=57% | |
248 | DOXORUBICIN METABOLIC PROCESS | 8 | -0.68 | -1.47 | 0.082 | 0.692 | 1.000 | 2655 | tags=50%, list=13%, signal=57% | |
249 | NEUROTRANSMITTER TRANSPORT | 69 | -0.40 | -1.47 | 0.035 | 0.693 | 1.000 | 3220 | tags=36%, list=16%, signal=43% | |
250 | NEGATIVE REGULATION OF CELLULAR CARBOHYDRATE METABOLIC PROCESS | 21 | -0.51 | -1.47 | 0.061 | 0.698 | 1.000 | 3000 | tags=38%, list=15%, signal=45% | |
251 | POSITIVE REGULATION OF POSITIVE CHEMOTAXIS | 11 | -0.54 | -1.47 | 0.053 | 0.697 | 1.000 | 2822 | tags=45%, list=14%, signal=53% | |
252 | REGULATION OF CYCLASE ACTIVITY | 51 | -0.43 | -1.47 | 0.080 | 0.694 | 1.000 | 4147 | tags=43%, list=20%, signal=54% | |
253 | GENITALIA MORPHOGENESIS | 10 | -0.55 | -1.47 | 0.058 | 0.692 | 1.000 | 4914 | tags=40%, list=24%, signal=53% | |
254 | KERATAN SULFATE BIOSYNTHETIC PROCESS | 26 | -0.45 | -1.47 | 0.078 | 0.692 | 1.000 | 3463 | tags=35%, list=17%, signal=42% | |
255 | POSITIVE REGULATION OF CELLULAR AMINO ACID METABOLIC PROCESS | 5 | -0.73 | -1.47 | 0.055 | 0.690 | 1.000 | 4557 | tags=80%, list=22%, signal=103% | |
256 | CELL JUNCTION ORGANIZATION | 143 | -0.36 | -1.47 | 0.034 | 0.688 | 1.000 | 4853 | tags=36%, list=24%, signal=47% | |
257 | DERMATAN SULFATE PROTEOGLYCAN METABOLIC PROCESS | 9 | -0.65 | -1.47 | 0.061 | 0.686 | 1.000 | 3927 | tags=56%, list=19%, signal=69% | |
258 | FUCOSYLATION | 20 | -0.49 | -1.47 | 0.030 | 0.684 | 1.000 | 6759 | tags=60%, list=33%, signal=89% | |
259 | POSITIVE REGULATION OF GLYCOGEN METABOLIC PROCESS | 13 | -0.53 | -1.47 | 0.064 | 0.683 | 1.000 | 5094 | tags=46%, list=25%, signal=61% | |
260 | SEX DETERMINATION | 21 | -0.48 | -1.47 | 0.063 | 0.681 | 1.000 | 5050 | tags=52%, list=25%, signal=69% | |
261 | REGULATION OF CYCLIC NUCLEOTIDE METABOLIC PROCESS | 92 | -0.40 | -1.47 | 0.055 | 0.679 | 1.000 | 5416 | tags=43%, list=26%, signal=59% | |
262 | DIGESTIVE TRACT DEVELOPMENT | 107 | -0.35 | -1.47 | 0.025 | 0.685 | 1.000 | 3815 | tags=32%, list=19%, signal=39% | |
263 | REGULATION OF AXON DIAMETER | 5 | -0.74 | -1.47 | 0.063 | 0.686 | 1.000 | 5311 | tags=100%, list=26%, signal=135% | |
264 | REGULATION OF CELL PROJECTION SIZE | 5 | -0.74 | -1.47 | 0.063 | 0.683 | 1.000 | 5311 | tags=100%, list=26%, signal=135% | |
265 | REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE BY HORMONE | 23 | -0.51 | -1.47 | 0.064 | 0.682 | 1.000 | 3574 | tags=43%, list=17%, signal=53% | |
266 | MIDBRAIN DOPAMINERGIC NEURON DIFFERENTIATION | 6 | -0.68 | -1.47 | 0.077 | 0.682 | 1.000 | 1470 | tags=33%, list=7%, signal=36% | |
267 | EMBRYONIC SKELETAL JOINT DEVELOPMENT | 16 | -0.53 | -1.46 | 0.060 | 0.682 | 1.000 | 3799 | tags=44%, list=18%, signal=54% | |
268 | MALE GENITALIA DEVELOPMENT | 23 | -0.49 | -1.46 | 0.064 | 0.682 | 1.000 | 5437 | tags=52%, list=26%, signal=71% | |
269 | HEMIDESMOSOME ASSEMBLY | 11 | -0.61 | -1.46 | 0.062 | 0.680 | 1.000 | 3694 | tags=55%, list=18%, signal=66% | |
270 | BLOOD COAGULATION, EXTRINSIC PATHWAY | 5 | -0.70 | -1.46 | 0.073 | 0.682 | 1.000 | 2822 | tags=60%, list=14%, signal=70% | |
271 | POSITIVE REGULATION OF CELLULAR RESPONSE TO OXIDATIVE STRESS | 9 | -0.59 | -1.46 | 0.074 | 0.681 | 1.000 | 3982 | tags=44%, list=19%, signal=55% | |
272 | POSITIVE REGULATION OF RESPONSE TO OXIDATIVE STRESS | 9 | -0.59 | -1.46 | 0.074 | 0.679 | 1.000 | 3982 | tags=44%, list=19%, signal=55% | |
273 | LIPID HOMEOSTASIS | 65 | -0.39 | -1.46 | 0.028 | 0.679 | 1.000 | 4843 | tags=38%, list=24%, signal=50% | |
274 | NEGATIVE REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 13 | -0.51 | -1.46 | 0.060 | 0.677 | 1.000 | 4667 | tags=46%, list=23%, signal=60% | |
275 | PROTEIN O-LINKED FUCOSYLATION | 10 | -0.60 | -1.46 | 0.068 | 0.675 | 1.000 | 5990 | tags=70%, list=29%, signal=99% | |
276 | REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS | 16 | -0.53 | -1.46 | 0.087 | 0.674 | 1.000 | 7282 | tags=63%, list=35%, signal=97% | |
277 | ONE-CARBON COMPOUND TRANSPORT | 5 | -0.76 | -1.46 | 0.063 | 0.676 | 1.000 | 3625 | tags=80%, list=18%, signal=97% | |
278 | DISTAL TUBULE DEVELOPMENT | 8 | -0.64 | -1.46 | 0.067 | 0.675 | 1.000 | 1797 | tags=38%, list=9%, signal=41% | |
279 | METANEPHRIC TUBULE FORMATION | 6 | -0.67 | -1.46 | 0.075 | 0.678 | 1.000 | 6755 | tags=83%, list=33%, signal=124% | |
280 | DERMATAN SULFATE METABOLIC PROCESS | 8 | -0.66 | -1.46 | 0.071 | 0.676 | 1.000 | 3258 | tags=50%, list=16%, signal=59% | |
281 | CONVERGENT EXTENSION INVOLVED IN GASTRULATION | 8 | -0.64 | -1.46 | 0.079 | 0.677 | 1.000 | 1192 | tags=38%, list=6%, signal=40% | |
282 | SYMPATHETIC NERVOUS SYSTEM DEVELOPMENT | 20 | -0.45 | -1.46 | 0.085 | 0.681 | 1.000 | 6400 | tags=40%, list=31%, signal=58% | |
283 | NEURON MATURATION | 28 | -0.45 | -1.46 | 0.077 | 0.680 | 1.000 | 4820 | tags=46%, list=23%, signal=61% | |
284 | NEGATIVE REGULATION OF LIPOPROTEIN PARTICLE CLEARANCE | 5 | -0.77 | -1.46 | 0.030 | 0.679 | 1.000 | 4352 | tags=80%, list=21%, signal=101% | |
285 | POSITIVE REGULATION OF NATURAL KILLER CELL MEDIATED IMMUNITY | 15 | -0.55 | -1.46 | 0.117 | 0.678 | 1.000 | 3208 | tags=33%, list=16%, signal=39% | |
286 | OVULATION CYCLE PROCESS | 59 | -0.35 | -1.46 | 0.029 | 0.678 | 1.000 | 4327 | tags=32%, list=21%, signal=41% | |
287 | CELLULAR RESPONSE TO STEROL | 9 | -0.63 | -1.46 | 0.078 | 0.677 | 1.000 | 3327 | tags=44%, list=16%, signal=53% | |
288 | COLLECTING DUCT DEVELOPMENT | 7 | -0.67 | -1.45 | 0.060 | 0.678 | 1.000 | 2656 | tags=57%, list=13%, signal=66% | |
289 | REGULATION OF LIPASE ACTIVITY | 88 | -0.35 | -1.45 | 0.017 | 0.676 | 1.000 | 4407 | tags=35%, list=21%, signal=45% | |
290 | POSITIVE REGULATION OF VESICLE FUSION | 5 | -0.72 | -1.45 | 0.063 | 0.675 | 1.000 | 516 | tags=20%, list=3%, signal=21% | |
291 | PREGANGLIONIC PARASYMPATHETIC FIBER DEVELOPMENT | 15 | -0.54 | -1.45 | 0.081 | 0.673 | 1.000 | 5056 | tags=47%, list=25%, signal=62% | |
292 | PROSTATE GLANDULAR ACINUS DEVELOPMENT | 11 | -0.56 | -1.45 | 0.081 | 0.676 | 1.000 | 5357 | tags=64%, list=26%, signal=86% | |
293 | INNER CELL MASS CELL DIFFERENTIATION | 6 | -0.58 | -1.45 | 0.052 | 0.675 | 1.000 | 907 | tags=33%, list=4%, signal=35% | |
294 | RESPONSE TO COPPER ION | 9 | -0.59 | -1.45 | 0.066 | 0.673 | 1.000 | 3963 | tags=44%, list=19%, signal=55% | |
295 | EPITHELIAL STRUCTURE MAINTENANCE | 8 | -0.62 | -1.45 | 0.067 | 0.676 | 1.000 | 5139 | tags=63%, list=25%, signal=83% | |
296 | NEGATIVE REGULATION OF BMP SIGNALING PATHWAY | 21 | -0.44 | -1.45 | 0.049 | 0.681 | 1.000 | 5856 | tags=52%, list=28%, signal=73% | |
297 | BLASTOCYST FORMATION | 33 | -0.40 | -1.45 | 0.038 | 0.683 | 1.000 | 3677 | tags=33%, list=18%, signal=41% | |
298 | REGULATION OF HYDROGEN PEROXIDE METABOLIC PROCESS | 9 | -0.63 | -1.45 | 0.100 | 0.682 | 1.000 | 4302 | tags=56%, list=21%, signal=70% | |
299 | MUSCLE STRUCTURE DEVELOPMENT | 384 | -0.33 | -1.45 | 0.016 | 0.685 | 1.000 | 4163 | tags=32%, list=20%, signal=39% | |
300 | REGULATION OF COLLATERAL SPROUTING | 16 | -0.49 | -1.45 | 0.053 | 0.688 | 1.000 | 5634 | tags=38%, list=27%, signal=52% | |
301 | POSITIVE REGULATION OF HUMORAL IMMUNE RESPONSE | 7 | -0.66 | -1.45 | 0.070 | 0.689 | 1.000 | 2977 | tags=57%, list=14%, signal=67% | |
302 | NEUROLOGICAL SYSTEM PROCESS INVOLVED IN REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE | 5 | -0.72 | -1.44 | 0.070 | 0.699 | 1.000 | 3494 | tags=40%, list=17%, signal=48% | |
303 | GAMMA-AMINOBUTYRIC ACID SIGNALING PATHWAY | 6 | -0.66 | -1.44 | 0.081 | 0.701 | 1.000 | 2131 | tags=33%, list=10%, signal=37% | |
304 | LUNG VASCULATURE DEVELOPMENT | 8 | -0.59 | -1.44 | 0.087 | 0.699 | 1.000 | 8351 | tags=88%, list=41%, signal=147% | |
305 | SPINAL CORD DORSAL/VENTRAL PATTERNING | 23 | -0.51 | -1.44 | 0.094 | 0.698 | 1.000 | 6996 | tags=52%, list=34%, signal=79% | |
306 | SARCOMERE ORGANIZATION | 26 | -0.42 | -1.44 | 0.057 | 0.698 | 1.000 | 3869 | tags=31%, list=19%, signal=38% | |
307 | NEPHRON MORPHOGENESIS | 63 | -0.38 | -1.44 | 0.053 | 0.697 | 1.000 | 4557 | tags=40%, list=22%, signal=51% | |
308 | NEPHRON EPITHELIUM MORPHOGENESIS | 63 | -0.38 | -1.44 | 0.053 | 0.695 | 1.000 | 4557 | tags=40%, list=22%, signal=51% | |
309 | NEGATIVE REGULATION OF ASTROCYTE DIFFERENTIATION | 11 | -0.57 | -1.44 | 0.090 | 0.695 | 1.000 | 5090 | tags=45%, list=25%, signal=60% | |
310 | PROTEIN-LIPID COMPLEX ASSEMBLY | 14 | -0.54 | -1.44 | 0.090 | 0.698 | 1.000 | 3662 | tags=50%, list=18%, signal=61% | |
311 | NEPHRON TUBULE MORPHOGENESIS | 60 | -0.38 | -1.44 | 0.055 | 0.699 | 1.000 | 4557 | tags=40%, list=22%, signal=51% | |
312 | REGULATION OF POSTTRANSCRIPTIONAL GENE SILENCING | 9 | -0.55 | -1.44 | 0.094 | 0.697 | 1.000 | 1097 | tags=22%, list=5%, signal=23% | |
313 | REGULATION OF GENE SILENCING BY RNA | 9 | -0.55 | -1.44 | 0.094 | 0.695 | 1.000 | 1097 | tags=22%, list=5%, signal=23% | |
314 | FOREGUT MORPHOGENESIS | 12 | -0.52 | -1.44 | 0.070 | 0.694 | 1.000 | 6301 | tags=67%, list=31%, signal=96% | |
315 | EMBRYONIC FOREGUT MORPHOGENESIS | 11 | -0.56 | -1.44 | 0.096 | 0.694 | 1.000 | 6301 | tags=73%, list=31%, signal=105% | |
316 | PHOSPHOLIPID EFFLUX | 11 | -0.63 | -1.44 | 0.118 | 0.693 | 1.000 | 3581 | tags=55%, list=17%, signal=66% | |
317 | NEGATIVE REGULATION OF GLYCOGEN METABOLIC PROCESS | 6 | -0.69 | -1.44 | 0.088 | 0.692 | 1.000 | 2938 | tags=67%, list=14%, signal=78% | |
318 | NEGATIVE REGULATION OF LIPOPOLYSACCHARIDE-MEDIATED SIGNALING PATHWAY | 5 | -0.68 | -1.44 | 0.062 | 0.693 | 1.000 | 4857 | tags=40%, list=24%, signal=52% | |
319 | METANEPHRIC NEPHRON DEVELOPMENT | 25 | -0.47 | -1.44 | 0.098 | 0.693 | 1.000 | 3849 | tags=44%, list=19%, signal=54% | |
320 | OVULATION CYCLE | 60 | -0.35 | -1.43 | 0.039 | 0.697 | 1.000 | 4327 | tags=32%, list=21%, signal=40% | |
321 | TERPENOID METABOLIC PROCESS | 70 | -0.39 | -1.43 | 0.082 | 0.699 | 1.000 | 5651 | tags=43%, list=27%, signal=59% | |
322 | POSITIVE REGULATION OF SMAD PROTEIN IMPORT INTO NUCLEUS | 10 | -0.60 | -1.43 | 0.111 | 0.699 | 1.000 | 4850 | tags=60%, list=24%, signal=78% | |
323 | T-HELPER 17 TYPE IMMUNE RESPONSE | 7 | -0.71 | -1.43 | 0.069 | 0.702 | 1.000 | 3046 | tags=29%, list=15%, signal=34% | |
324 | T-HELPER 17 CELL DIFFERENTIATION | 7 | -0.71 | -1.43 | 0.069 | 0.700 | 1.000 | 3046 | tags=29%, list=15%, signal=34% | |
325 | REGULATION OF ODONTOGENESIS | 9 | -0.59 | -1.43 | 0.089 | 0.699 | 1.000 | 6188 | tags=78%, list=30%, signal=111% | |
326 | LIPID DIGESTION | 14 | -0.56 | -1.43 | 0.069 | 0.703 | 1.000 | 2655 | tags=43%, list=13%, signal=49% | |
327 | MESONEPHROS DEVELOPMENT | 74 | -0.37 | -1.43 | 0.047 | 0.710 | 1.000 | 4745 | tags=41%, list=23%, signal=52% | |
328 | RESPONSE TO PAIN | 6 | -0.65 | -1.43 | 0.091 | 0.709 | 1.000 | 5990 | tags=83%, list=29%, signal=117% | |
329 | DEVELOPMENTAL GROWTH INVOLVED IN MORPHOGENESIS | 98 | -0.35 | -1.43 | 0.045 | 0.710 | 1.000 | 2805 | tags=27%, list=14%, signal=31% | |
330 | CARDIAC MYOFIBRIL ASSEMBLY | 14 | -0.52 | -1.42 | 0.069 | 0.717 | 1.000 | 5582 | tags=57%, list=27%, signal=78% | |
331 | RADIAL GLIAL CELL DIFFERENTIATION | 10 | -0.54 | -1.42 | 0.067 | 0.715 | 1.000 | 5383 | tags=50%, list=26%, signal=68% | |
332 | INNERVATION | 22 | -0.47 | -1.42 | 0.099 | 0.713 | 1.000 | 5279 | tags=41%, list=26%, signal=55% | |
333 | POSITIVE REGULATION OF CARDIAC MUSCLE HYPERTROPHY | 14 | -0.50 | -1.42 | 0.087 | 0.713 | 1.000 | 6175 | tags=50%, list=30%, signal=71% | |
334 | POSITIVE REGULATION OF MUSCLE HYPERTROPHY | 14 | -0.50 | -1.42 | 0.087 | 0.711 | 1.000 | 6175 | tags=50%, list=30%, signal=71% | |
335 | REGULATION OF POLYSACCHARIDE BIOSYNTHETIC PROCESS | 24 | -0.47 | -1.42 | 0.089 | 0.710 | 1.000 | 4049 | tags=38%, list=20%, signal=47% | |
336 | DOPAMINERGIC NEURON DIFFERENTIATION | 24 | -0.48 | -1.42 | 0.090 | 0.710 | 1.000 | 4377 | tags=42%, list=21%, signal=53% | |
337 | CYTOKINE METABOLIC PROCESS | 8 | -0.59 | -1.42 | 0.104 | 0.712 | 1.000 | 2650 | tags=50%, list=13%, signal=57% | |
338 | AMINO ACID IMPORT | 6 | -0.70 | -1.42 | 0.071 | 0.711 | 1.000 | 1864 | tags=50%, list=9%, signal=55% | |
339 | NEGATIVE REGULATION OF AXON EXTENSION INVOLVED IN AXON GUIDANCE | 8 | -0.59 | -1.42 | 0.093 | 0.709 | 1.000 | 7038 | tags=75%, list=34%, signal=114% | |
340 | MAMMARY GLAND FORMATION | 9 | -0.63 | -1.42 | 0.104 | 0.707 | 1.000 | 3815 | tags=67%, list=19%, signal=82% | |
341 | AXIAL MESODERM DEVELOPMENT | 8 | -0.60 | -1.42 | 0.091 | 0.706 | 1.000 | 3799 | tags=50%, list=18%, signal=61% | |
342 | REGIONALIZATION | 286 | -0.33 | -1.42 | 0.036 | 0.712 | 1.000 | 6537 | tags=43%, list=32%, signal=62% | |
343 | NEGATIVE REGULATION OF ENDOTHELIAL CELL APOPTOTIC PROCESS | 20 | -0.48 | -1.42 | 0.076 | 0.719 | 1.000 | 4868 | tags=45%, list=24%, signal=59% | |
344 | T CELL LINEAGE COMMITMENT | 16 | -0.50 | -1.42 | 0.082 | 0.717 | 1.000 | 3814 | tags=38%, list=19%, signal=46% | |
345 | REGULATION OF AXON EXTENSION INVOLVED IN AXON GUIDANCE | 11 | -0.52 | -1.42 | 0.082 | 0.719 | 1.000 | 1322 | tags=36%, list=6%, signal=39% | |
346 | WOUND HEALING, SPREADING OF CELLS | 17 | -0.48 | -1.42 | 0.065 | 0.717 | 1.000 | 5311 | tags=47%, list=26%, signal=63% | |
347 | EPIBOLY INVOLVED IN WOUND HEALING | 17 | -0.48 | -1.42 | 0.065 | 0.715 | 1.000 | 5311 | tags=47%, list=26%, signal=63% | |
348 | DITERPENOID METABOLIC PROCESS | 64 | -0.39 | -1.42 | 0.090 | 0.714 | 1.000 | 5414 | tags=41%, list=26%, signal=55% | |
349 | GASTRULATION | 143 | -0.32 | -1.42 | 0.034 | 0.714 | 1.000 | 4389 | tags=29%, list=21%, signal=37% | |
350 | VENTRAL SPINAL CORD INTERNEURON FATE COMMITMENT | 14 | -0.58 | -1.42 | 0.118 | 0.713 | 1.000 | 6996 | tags=57%, list=34%, signal=86% | |
351 | CELL FATE COMMITMENT INVOLVED IN PATTERN SPECIFICATION | 14 | -0.58 | -1.42 | 0.118 | 0.711 | 1.000 | 6996 | tags=57%, list=34%, signal=86% | |
352 | REGULATION OF CGMP BIOSYNTHETIC PROCESS | 8 | -0.64 | -1.41 | 0.106 | 0.714 | 1.000 | 4575 | tags=63%, list=22%, signal=80% | |
353 | SPERM MOTILITY | 21 | -0.46 | -1.41 | 0.063 | 0.713 | 1.000 | 6459 | tags=48%, list=31%, signal=69% | |
354 | NEUROTRANSMITTER SECRETION | 62 | -0.39 | -1.41 | 0.059 | 0.716 | 1.000 | 3220 | tags=37%, list=16%, signal=44% | |
355 | REGULATION OF INTERLEUKIN-17 PRODUCTION | 18 | -0.50 | -1.41 | 0.106 | 0.715 | 1.000 | 5139 | tags=44%, list=25%, signal=59% | |
356 | CHYLOMICRON REMNANT CLEARANCE | 5 | -0.76 | -1.41 | 0.084 | 0.713 | 1.000 | 3581 | tags=80%, list=17%, signal=97% | |
357 | TRIGLYCERIDE-RICH LIPOPROTEIN PARTICLE CLEARANCE | 5 | -0.76 | -1.41 | 0.084 | 0.711 | 1.000 | 3581 | tags=80%, list=17%, signal=97% | |
358 | REGULATION OF CARDIAC MUSCLE HYPERTROPHY | 20 | -0.46 | -1.41 | 0.084 | 0.710 | 1.000 | 7047 | tags=50%, list=34%, signal=76% | |
359 | REGULATION OF MUSCLE HYPERTROPHY | 20 | -0.46 | -1.41 | 0.084 | 0.708 | 1.000 | 7047 | tags=50%, list=34%, signal=76% | |
360 | POSITIVE REGULATION OF PROTEIN KINASE B SIGNALING | 51 | -0.39 | -1.41 | 0.046 | 0.712 | 1.000 | 6356 | tags=53%, list=31%, signal=76% | |
361 | REGULATION OF GLYCOGEN METABOLIC PROCESS | 21 | -0.48 | -1.41 | 0.100 | 0.713 | 1.000 | 5537 | tags=48%, list=27%, signal=65% | |
362 | OLIGOSACCHARIDE CATABOLIC PROCESS | 5 | -0.71 | -1.41 | 0.081 | 0.715 | 1.000 | 1303 | tags=60%, list=6%, signal=64% | |
363 | REGULATION OF ENDOCYTIC RECYCLING | 6 | -0.62 | -1.41 | 0.091 | 0.714 | 1.000 | 4050 | tags=50%, list=20%, signal=62% | |
364 | REGULATION OF PURINE NUCLEOTIDE METABOLIC PROCESS | 119 | -0.35 | -1.41 | 0.035 | 0.719 | 1.000 | 5264 | tags=40%, list=26%, signal=54% | |
365 | CELLULAR RESPONSE TO LEPTIN STIMULUS | 10 | -0.54 | -1.41 | 0.054 | 0.722 | 1.000 | 4896 | tags=50%, list=24%, signal=66% | |
366 | NEGATIVE CHEMOTAXIS | 17 | -0.48 | -1.41 | 0.113 | 0.720 | 1.000 | 1213 | tags=24%, list=6%, signal=25% | |
367 | REGULATION OF INTERFERON-GAMMA SECRETION | 7 | -0.63 | -1.41 | 0.108 | 0.722 | 1.000 | 5 | tags=14%, list=0%, signal=14% | |
368 | RENAL SYSTEM VASCULATURE MORPHOGENESIS | 6 | -0.68 | -1.40 | 0.113 | 0.725 | 1.000 | 3849 | tags=67%, list=19%, signal=82% | |
369 | KIDNEY VASCULATURE MORPHOGENESIS | 6 | -0.68 | -1.40 | 0.113 | 0.723 | 1.000 | 3849 | tags=67%, list=19%, signal=82% | |
370 | REGULATION OF NK T CELL ACTIVATION | 5 | -0.63 | -1.40 | 0.102 | 0.722 | 1.000 | 3536 | tags=40%, list=17%, signal=48% | |
371 | IMMUNOLOGICAL SYNAPSE FORMATION | 5 | -0.73 | -1.40 | 0.073 | 0.720 | 1.000 | 5601 | tags=100%, list=27%, signal=137% | |
372 | PARAXIAL MESODERM DEVELOPMENT | 18 | -0.45 | -1.40 | 0.083 | 0.720 | 1.000 | 6710 | tags=50%, list=33%, signal=74% | |
373 | EXOGENOUS DRUG CATABOLIC PROCESS | 9 | -0.58 | -1.40 | 0.131 | 0.719 | 1.000 | 6407 | tags=67%, list=31%, signal=97% | |
374 | NEGATIVE REGULATION OF OSTEOCLAST DIFFERENTIATION | 10 | -0.57 | -1.40 | 0.083 | 0.717 | 1.000 | 2350 | tags=30%, list=11%, signal=34% | |
375 | COLLATERAL SPROUTING | 9 | -0.57 | -1.40 | 0.111 | 0.717 | 1.000 | 3469 | tags=56%, list=17%, signal=67% | |
376 | CELLULAR RESPONSE TO CHOLESTEROL | 7 | -0.63 | -1.40 | 0.109 | 0.715 | 1.000 | 3327 | tags=57%, list=16%, signal=68% | |
377 | CEREBRAL CORTEX GABAERGIC INTERNEURON DEVELOPMENT | 8 | -0.65 | -1.40 | 0.110 | 0.722 | 1.000 | 743 | tags=38%, list=4%, signal=39% | |
378 | POSITIVE REGULATION OF AXONOGENESIS | 54 | -0.37 | -1.40 | 0.058 | 0.720 | 1.000 | 3818 | tags=33%, list=19%, signal=41% | |
379 | REGULATION OF GLUCONEOGENESIS | 9 | -0.55 | -1.40 | 0.105 | 0.720 | 1.000 | 3690 | tags=44%, list=18%, signal=54% | |
380 | REGULATION OF ACTIN CYTOSKELETON REORGANIZATION | 21 | -0.50 | -1.40 | 0.117 | 0.719 | 1.000 | 5173 | tags=52%, list=25%, signal=70% | |
381 | REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 27 | -0.47 | -1.40 | 0.101 | 0.723 | 1.000 | 5050 | tags=41%, list=25%, signal=54% | |
382 | POSITIVE REGULATION OF LIPASE ACTIVITY | 76 | -0.34 | -1.40 | 0.030 | 0.727 | 1.000 | 4407 | tags=34%, list=21%, signal=43% | |
383 | REGULATION OF MHC CLASS II BIOSYNTHETIC PROCESS | 6 | -0.66 | -1.40 | 0.096 | 0.726 | 1.000 | 1120 | tags=33%, list=5%, signal=35% | |
384 | TRANSEPITHELIAL TRANSPORT | 9 | -0.57 | -1.40 | 0.102 | 0.735 | 1.000 | 2971 | tags=33%, list=14%, signal=39% | |
385 | CARDIOBLAST DIFFERENTIATION | 12 | -0.54 | -1.40 | 0.120 | 0.733 | 1.000 | 6094 | tags=58%, list=30%, signal=83% | |
386 | SINGLE FERTILIZATION | 38 | -0.41 | -1.39 | 0.090 | 0.732 | 1.000 | 6459 | tags=58%, list=31%, signal=84% | |
387 | NEGATIVE REGULATION OF REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 9 | -0.57 | -1.39 | 0.118 | 0.732 | 1.000 | 5989 | tags=56%, list=29%, signal=78% | |
388 | REGULATION OF STRESS FIBER ASSEMBLY | 43 | -0.38 | -1.39 | 0.050 | 0.731 | 1.000 | 2524 | tags=30%, list=12%, signal=34% | |
389 | SMOOTHENED SIGNALING PATHWAY | 27 | -0.41 | -1.39 | 0.086 | 0.730 | 1.000 | 6616 | tags=59%, list=32%, signal=87% | |
390 | POSITIVE REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS | 10 | -0.56 | -1.39 | 0.118 | 0.729 | 1.000 | 7282 | tags=60%, list=35%, signal=93% | |
391 | STRIATED MUSCLE TISSUE DEVELOPMENT | 228 | -0.31 | -1.39 | 0.022 | 0.728 | 1.000 | 4163 | tags=30%, list=20%, signal=37% | |
392 | POLYOL BIOSYNTHETIC PROCESS | 8 | -0.55 | -1.39 | 0.116 | 0.728 | 1.000 | 896 | tags=25%, list=4%, signal=26% | |
393 | CHOLESTEROL HOMEOSTASIS | 42 | -0.40 | -1.39 | 0.047 | 0.727 | 1.000 | 4843 | tags=40%, list=24%, signal=53% | |
394 | STEROL HOMEOSTASIS | 42 | -0.40 | -1.39 | 0.047 | 0.725 | 1.000 | 4843 | tags=40%, list=24%, signal=53% | |
395 | CYTOKINE BIOSYNTHETIC PROCESS | 7 | -0.62 | -1.39 | 0.095 | 0.724 | 1.000 | 2650 | tags=57%, list=13%, signal=66% | |
396 | REGULATION OF PHOSPHOLIPASE ACTIVITY | 75 | -0.34 | -1.39 | 0.039 | 0.722 | 1.000 | 4407 | tags=33%, list=21%, signal=42% | |
397 | G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 391 | -0.34 | -1.39 | 0.064 | 0.721 | 1.000 | 5988 | tags=41%, list=29%, signal=56% | |
398 | POSITIVE REGULATION OF ACTIN CYTOSKELETON REORGANIZATION | 11 | -0.58 | -1.39 | 0.128 | 0.730 | 1.000 | 3742 | tags=55%, list=18%, signal=67% | |
399 | POSITIVE REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 31 | -0.41 | -1.39 | 0.086 | 0.730 | 1.000 | 6887 | tags=55%, list=33%, signal=82% | |
400 | PYRIMIDINE DEOXYRIBONUCLEOTIDE CATABOLIC PROCESS | 10 | -0.57 | -1.39 | 0.133 | 0.730 | 1.000 | 2575 | tags=50%, list=12%, signal=57% | |
401 | DNA METHYLATION INVOLVED IN GAMETE GENERATION | 14 | -0.50 | -1.39 | 0.108 | 0.730 | 1.000 | 3680 | tags=21%, list=18%, signal=26% | |
402 | COMMISSURAL NEURON AXON GUIDANCE | 7 | -0.56 | -1.39 | 0.114 | 0.729 | 1.000 | 4336 | tags=43%, list=21%, signal=54% | |
403 | RENAL TUBULE MORPHOGENESIS | 65 | -0.36 | -1.39 | 0.065 | 0.729 | 1.000 | 4557 | tags=38%, list=22%, signal=49% | |
404 | BONE TRABECULA FORMATION | 8 | -0.58 | -1.39 | 0.114 | 0.728 | 1.000 | 3797 | tags=50%, list=18%, signal=61% | |
405 | METANEPHROS DEVELOPMENT | 68 | -0.38 | -1.39 | 0.088 | 0.727 | 1.000 | 7193 | tags=54%, list=35%, signal=83% | |
406 | MUSCLE TISSUE DEVELOPMENT | 244 | -0.31 | -1.39 | 0.025 | 0.727 | 1.000 | 4163 | tags=30%, list=20%, signal=37% | |
407 | MESODERM FORMATION | 61 | -0.36 | -1.39 | 0.060 | 0.729 | 1.000 | 4389 | tags=33%, list=21%, signal=42% | |
408 | REGULATION OF SMOOTH MUSCLE CELL DIFFERENTIATION | 8 | -0.58 | -1.38 | 0.116 | 0.734 | 1.000 | 5287 | tags=63%, list=26%, signal=84% | |
409 | T CELL APOPTOTIC PROCESS | 5 | -0.71 | -1.38 | 0.101 | 0.735 | 1.000 | 3650 | tags=60%, list=18%, signal=73% | |
410 | INORGANIC ANION TRANSMEMBRANE TRANSPORT | 55 | -0.40 | -1.38 | 0.094 | 0.736 | 1.000 | 6111 | tags=40%, list=30%, signal=57% | |
411 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER INVOLVED IN HEART DEVELOPMENT | 5 | -0.57 | -1.38 | 0.103 | 0.735 | 1.000 | 5430 | tags=60%, list=26%, signal=81% | |
412 | RESPONSE TO PROSTAGLANDIN E | 10 | -0.56 | -1.38 | 0.134 | 0.735 | 1.000 | 5951 | tags=60%, list=29%, signal=84% | |
413 | FERTILIZATION | 41 | -0.40 | -1.38 | 0.090 | 0.735 | 1.000 | 6459 | tags=54%, list=31%, signal=78% | |
414 | DERMATAN SULFATE PROTEOGLYCAN BIOSYNTHETIC PROCESS | 8 | -0.62 | -1.38 | 0.105 | 0.733 | 1.000 | 3927 | tags=50%, list=19%, signal=62% | |
415 | EMBRYONIC BRAIN DEVELOPMENT | 8 | -0.55 | -1.38 | 0.105 | 0.732 | 1.000 | 6350 | tags=50%, list=31%, signal=72% | |
416 | POSITIVE REGULATION OF MESONEPHROS DEVELOPMENT | 14 | -0.50 | -1.38 | 0.098 | 0.730 | 1.000 | 6755 | tags=71%, list=33%, signal=106% | |
417 | CAMP CATABOLIC PROCESS | 7 | -0.61 | -1.38 | 0.121 | 0.729 | 1.000 | 793 | tags=29%, list=4%, signal=30% | |
418 | PHOSPHOLIPID HOMEOSTASIS | 8 | -0.61 | -1.38 | 0.111 | 0.727 | 1.000 | 2222 | tags=38%, list=11%, signal=42% | |
419 | RETINOID METABOLIC PROCESS | 62 | -0.39 | -1.38 | 0.109 | 0.728 | 1.000 | 5414 | tags=40%, list=26%, signal=55% | |
420 | PROTEIN HETEROOLIGOMERIZATION | 30 | -0.41 | -1.38 | 0.073 | 0.727 | 1.000 | 6147 | tags=43%, list=30%, signal=62% | |
421 | POSITIVE REGULATION OF BLOOD PRESSURE | 6 | -0.64 | -1.38 | 0.112 | 0.727 | 1.000 | 7372 | tags=100%, list=36%, signal=156% | |
422 | NEGATIVE REGULATION OF HEART RATE | 5 | -0.64 | -1.38 | 0.113 | 0.729 | 1.000 | 4519 | tags=40%, list=22%, signal=51% | |
423 | LUNG LOBE DEVELOPMENT | 9 | -0.54 | -1.38 | 0.130 | 0.729 | 1.000 | 3580 | tags=67%, list=17%, signal=81% | |
424 | LUNG LOBE MORPHOGENESIS | 9 | -0.54 | -1.38 | 0.130 | 0.728 | 1.000 | 3580 | tags=67%, list=17%, signal=81% | |
425 | MOLTING CYCLE | 90 | -0.33 | -1.38 | 0.054 | 0.728 | 1.000 | 4739 | tags=36%, list=23%, signal=46% | |
426 | HAIR CYCLE | 90 | -0.33 | -1.38 | 0.054 | 0.726 | 1.000 | 4739 | tags=36%, list=23%, signal=46% | |
427 | REGULATION OF B CELL DIFFERENTIATION | 9 | -0.53 | -1.38 | 0.086 | 0.727 | 1.000 | 1716 | tags=33%, list=8%, signal=36% | |
428 | PROSTATE GLAND DEVELOPMENT | 41 | -0.39 | -1.38 | 0.079 | 0.733 | 1.000 | 5358 | tags=46%, list=26%, signal=63% | |
429 | MESODERM DEVELOPMENT | 105 | -0.32 | -1.38 | 0.069 | 0.733 | 1.000 | 4600 | tags=33%, list=22%, signal=43% | |
430 | REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE/THREONINE KINASE SIGNALING PATHWAY | 127 | -0.31 | -1.38 | 0.044 | 0.734 | 1.000 | 5023 | tags=33%, list=24%, signal=43% | |
431 | POSITIVE REGULATION OF AXON EXTENSION INVOLVED IN AXON GUIDANCE | 5 | -0.63 | -1.38 | 0.103 | 0.735 | 1.000 | 1322 | tags=60%, list=6%, signal=64% | |
432 | POSITIVE REGULATION OF AXON GUIDANCE | 5 | -0.63 | -1.38 | 0.103 | 0.734 | 1.000 | 1322 | tags=60%, list=6%, signal=64% | |
433 | NEURAL PLATE PATTERN SPECIFICATION | 5 | -0.73 | -1.37 | 0.132 | 0.735 | 1.000 | 3799 | tags=60%, list=18%, signal=74% | |
434 | STRIATED MUSCLE CELL DEVELOPMENT | 96 | -0.32 | -1.37 | 0.047 | 0.734 | 1.000 | 4578 | tags=32%, list=22%, signal=41% | |
435 | ANATOMICAL STRUCTURE ARRANGEMENT | 20 | -0.46 | -1.37 | 0.115 | 0.733 | 1.000 | 7516 | tags=60%, list=36%, signal=94% | |
436 | REGULATION OF POLYSACCHARIDE METABOLIC PROCESS | 27 | -0.44 | -1.37 | 0.125 | 0.732 | 1.000 | 5650 | tags=44%, list=27%, signal=61% | |
437 | CRANIAL NERVE MORPHOGENESIS | 25 | -0.47 | -1.37 | 0.115 | 0.732 | 1.000 | 5056 | tags=48%, list=25%, signal=64% | |
438 | NEGATIVE REGULATION OF MONOOXYGENASE ACTIVITY | 9 | -0.61 | -1.37 | 0.138 | 0.735 | 1.000 | 1225 | tags=33%, list=6%, signal=35% | |
439 | POSITIVE REGULATION OF PEPTIDYL-TYROSINE PHOSPHORYLATION | 105 | -0.36 | -1.37 | 0.049 | 0.735 | 1.000 | 5650 | tags=37%, list=27%, signal=51% | |
440 | REGULATION OF BLOOD PRESSURE | 74 | -0.39 | -1.37 | 0.063 | 0.735 | 1.000 | 3574 | tags=35%, list=17%, signal=42% | |
441 | DIGESTIVE TRACT MORPHOGENESIS | 49 | -0.38 | -1.37 | 0.078 | 0.733 | 1.000 | 7048 | tags=51%, list=34%, signal=77% | |
442 | NEGATIVE REGULATION OF ORGAN GROWTH | 10 | -0.54 | -1.37 | 0.105 | 0.732 | 1.000 | 4163 | tags=60%, list=20%, signal=75% | |
443 | L-GLUTAMATE TRANSMEMBRANE TRANSPORT | 9 | -0.56 | -1.37 | 0.129 | 0.731 | 1.000 | 1864 | tags=44%, list=9%, signal=49% | |
444 | REGULATION OF NUCLEOTIDE METABOLIC PROCESS | 123 | -0.34 | -1.37 | 0.056 | 0.730 | 1.000 | 5264 | tags=39%, list=26%, signal=52% | |
445 | REGULATION OF CHOLESTEROL ESTERIFICATION | 8 | -0.64 | -1.37 | 0.156 | 0.731 | 1.000 | 5414 | tags=63%, list=26%, signal=85% | |
446 | URETERIC BUD MORPHOGENESIS | 52 | -0.36 | -1.37 | 0.095 | 0.733 | 1.000 | 4557 | tags=38%, list=22%, signal=49% | |
447 | NEPHRON TUBULE DEVELOPMENT | 65 | -0.35 | -1.37 | 0.084 | 0.737 | 1.000 | 4557 | tags=37%, list=22%, signal=47% | |
448 | FORMATION OF PRIMARY GERM LAYER | 102 | -0.33 | -1.37 | 0.085 | 0.737 | 1.000 | 3880 | tags=27%, list=19%, signal=34% | |
449 | POSITIVE REGULATION OF CELLULAR CARBOHYDRATE METABOLIC PROCESS | 30 | -0.39 | -1.37 | 0.072 | 0.736 | 1.000 | 4049 | tags=33%, list=20%, signal=41% | |
450 | REGULATION OF EPIDERMAL CELL DIFFERENTIATION | 28 | -0.40 | -1.37 | 0.104 | 0.735 | 1.000 | 2781 | tags=32%, list=13%, signal=37% | |
451 | MESODERMAL CELL FATE COMMITMENT | 13 | -0.51 | -1.37 | 0.146 | 0.733 | 1.000 | 4380 | tags=54%, list=21%, signal=68% | |
452 | RELEASE OF SEQUESTERED CALCIUM ION INTO CYTOSOL | 30 | -0.39 | -1.37 | 0.078 | 0.734 | 1.000 | 5630 | tags=43%, list=27%, signal=60% | |
453 | NEGATIVE REGULATION OF SEQUESTERING OF CALCIUM ION | 30 | -0.39 | -1.37 | 0.078 | 0.732 | 1.000 | 5630 | tags=43%, list=27%, signal=60% | |
454 | CALCIUM ION TRANSMEMBRANE IMPORT INTO CYTOSOL | 30 | -0.39 | -1.37 | 0.078 | 0.731 | 1.000 | 5630 | tags=43%, list=27%, signal=60% | |
455 | CALCIUM ION IMPORT INTO CYTOSOL | 30 | -0.39 | -1.37 | 0.078 | 0.729 | 1.000 | 5630 | tags=43%, list=27%, signal=60% | |
456 | NEGATIVE REGULATION OF FAT CELL DIFFERENTIATION | 21 | -0.45 | -1.37 | 0.089 | 0.728 | 1.000 | 7694 | tags=52%, list=37%, signal=84% | |
457 | CARDIOLIPIN ACYL-CHAIN REMODELING | 6 | -0.62 | -1.37 | 0.123 | 0.727 | 1.000 | 2230 | tags=50%, list=11%, signal=56% | |
458 | EMBRYONIC SKELETAL SYSTEM DEVELOPMENT | 126 | -0.34 | -1.37 | 0.089 | 0.726 | 1.000 | 4380 | tags=35%, list=21%, signal=44% | |
459 | RESPONSE TO RETINOIC ACID | 47 | -0.38 | -1.37 | 0.094 | 0.728 | 1.000 | 4076 | tags=36%, list=20%, signal=45% | |
460 | PYRIMIDINE NUCLEOTIDE CATABOLIC PROCESS | 11 | -0.55 | -1.37 | 0.148 | 0.727 | 1.000 | 2575 | tags=45%, list=12%, signal=52% | |
461 | NEGATIVE REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 25 | -0.44 | -1.36 | 0.092 | 0.727 | 1.000 | 2964 | tags=32%, list=14%, signal=37% | |
462 | HAIR FOLLICLE MORPHOGENESIS | 26 | -0.43 | -1.36 | 0.106 | 0.727 | 1.000 | 4460 | tags=35%, list=22%, signal=44% | |
463 | AXONOGENESIS INVOLVED IN INNERVATION | 6 | -0.66 | -1.36 | 0.139 | 0.727 | 1.000 | 2846 | tags=50%, list=14%, signal=58% | |
464 | CGMP METABOLIC PROCESS | 14 | -0.55 | -1.36 | 0.127 | 0.726 | 1.000 | 6673 | tags=64%, list=32%, signal=95% | |
465 | POSITIVE REGULATION OF COLLATERAL SPROUTING | 7 | -0.61 | -1.36 | 0.121 | 0.727 | 1.000 | 2653 | tags=43%, list=13%, signal=49% | |
466 | HINDGUT MORPHOGENESIS | 6 | -0.64 | -1.36 | 0.137 | 0.726 | 1.000 | 3650 | tags=50%, list=18%, signal=61% | |
467 | NEGATIVE REGULATION OF RHO PROTEIN SIGNAL TRANSDUCTION | 7 | -0.58 | -1.36 | 0.124 | 0.724 | 1.000 | 6053 | tags=57%, list=29%, signal=81% | |
468 | ADHERENS JUNCTION ASSEMBLY | 21 | -0.44 | -1.36 | 0.098 | 0.724 | 1.000 | 4566 | tags=48%, list=22%, signal=61% | |
469 | OOCYTE DEVELOPMENT | 20 | -0.42 | -1.36 | 0.075 | 0.724 | 1.000 | 5050 | tags=50%, list=25%, signal=66% | |
470 | MUSCLE CELL DIFFERENTIATION | 216 | -0.31 | -1.36 | 0.057 | 0.724 | 1.000 | 5776 | tags=41%, list=28%, signal=57% | |
471 | RETINOL METABOLIC PROCESS | 9 | -0.56 | -1.36 | 0.114 | 0.724 | 1.000 | 4577 | tags=44%, list=22%, signal=57% | |
472 | AMINO ACID TRANSMEMBRANE TRANSPORT | 35 | -0.44 | -1.36 | 0.103 | 0.724 | 1.000 | 1864 | tags=23%, list=9%, signal=25% | |
473 | REGULATION OF BRANCHING INVOLVED IN LUNG MORPHOGENESIS | 5 | -0.64 | -1.36 | 0.128 | 0.723 | 1.000 | 2252 | tags=40%, list=11%, signal=45% | |
474 | POSITIVE REGULATION OF PHOSPHOLIPASE ACTIVITY | 68 | -0.34 | -1.36 | 0.042 | 0.721 | 1.000 | 4407 | tags=34%, list=21%, signal=43% | |
475 | POSITIVE REGULATION OF TRIGLYCERIDE CATABOLIC PROCESS | 6 | -0.66 | -1.36 | 0.112 | 0.720 | 1.000 | 4193 | tags=67%, list=20%, signal=84% | |
476 | CGMP BIOSYNTHETIC PROCESS | 10 | -0.59 | -1.36 | 0.142 | 0.722 | 1.000 | 2829 | tags=40%, list=14%, signal=46% | |
477 | REGULATION OF NOTCH SIGNALING PATHWAY | 29 | -0.37 | -1.36 | 0.077 | 0.722 | 1.000 | 3982 | tags=38%, list=19%, signal=47% | |
478 | PROTEIN O-LINKED GLYCOSYLATION | 75 | -0.34 | -1.36 | 0.055 | 0.721 | 1.000 | 4087 | tags=37%, list=20%, signal=46% | |
479 | OOCYTE DIFFERENTIATION | 23 | -0.40 | -1.36 | 0.074 | 0.722 | 1.000 | 5617 | tags=52%, list=27%, signal=72% | |
480 | CRANIAL NERVE DEVELOPMENT | 41 | -0.40 | -1.36 | 0.116 | 0.722 | 1.000 | 5229 | tags=41%, list=25%, signal=55% | |
481 | G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY, COUPLED TO CYCLIC NUCLEOTIDE SECOND MESSENGER | 107 | -0.37 | -1.36 | 0.110 | 0.723 | 1.000 | 5983 | tags=40%, list=29%, signal=56% | |
482 | EPIDERMIS MORPHOGENESIS | 31 | -0.41 | -1.36 | 0.121 | 0.728 | 1.000 | 5581 | tags=39%, list=27%, signal=53% | |
483 | PROTEIN-LIPID COMPLEX SUBUNIT ORGANIZATION | 28 | -0.43 | -1.36 | 0.112 | 0.729 | 1.000 | 3662 | tags=39%, list=18%, signal=48% | |
484 | ARACHIDONIC ACID SECRETION | 8 | -0.60 | -1.36 | 0.155 | 0.728 | 1.000 | 3494 | tags=63%, list=17%, signal=75% | |
485 | ARACHIDONATE TRANSPORT | 8 | -0.60 | -1.36 | 0.155 | 0.726 | 1.000 | 3494 | tags=63%, list=17%, signal=75% | |
486 | UV PROTECTION | 9 | -0.55 | -1.36 | 0.126 | 0.725 | 1.000 | 2005 | tags=33%, list=10%, signal=37% | |
487 | REGULATION OF TRIGLYCERIDE CATABOLIC PROCESS | 8 | -0.61 | -1.36 | 0.116 | 0.724 | 1.000 | 4193 | tags=63%, list=20%, signal=78% | |
488 | HYPOTHALAMUS CELL MIGRATION | 5 | -0.68 | -1.36 | 0.139 | 0.724 | 1.000 | 2518 | tags=40%, list=12%, signal=46% | |
489 | MESONEPHRIC EPITHELIUM DEVELOPMENT | 71 | -0.35 | -1.36 | 0.085 | 0.724 | 1.000 | 4745 | tags=39%, list=23%, signal=51% | |
490 | MESONEPHRIC TUBULE DEVELOPMENT | 71 | -0.35 | -1.36 | 0.085 | 0.722 | 1.000 | 4745 | tags=39%, list=23%, signal=51% | |
491 | POSITIVE REGULATION OF MYELOID LEUKOCYTE CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 5 | -0.70 | -1.35 | 0.123 | 0.723 | 1.000 | 3534 | tags=60%, list=17%, signal=72% | |
492 | CALCIUM ION TRANSPORT | 128 | -0.33 | -1.35 | 0.091 | 0.722 | 1.000 | 5936 | tags=40%, list=29%, signal=56% | |
493 | CELL-CELL RECOGNITION | 25 | -0.43 | -1.35 | 0.120 | 0.721 | 1.000 | 6010 | tags=60%, list=29%, signal=85% | |
494 | LUNG MORPHOGENESIS | 49 | -0.34 | -1.35 | 0.079 | 0.719 | 1.000 | 4353 | tags=41%, list=21%, signal=52% | |
495 | SOMITE DEVELOPMENT | 66 | -0.33 | -1.35 | 0.067 | 0.721 | 1.000 | 3799 | tags=29%, list=18%, signal=35% | |
496 | COCHLEA MORPHOGENESIS | 22 | -0.47 | -1.35 | 0.121 | 0.720 | 1.000 | 4380 | tags=50%, list=21%, signal=63% | |
497 | LONG-CHAIN FATTY ACID BIOSYNTHETIC PROCESS | 7 | -0.63 | -1.35 | 0.136 | 0.719 | 1.000 | 683 | tags=29%, list=3%, signal=30% | |
498 | CONVERGENT EXTENSION | 15 | -0.52 | -1.35 | 0.145 | 0.719 | 1.000 | 2805 | tags=40%, list=14%, signal=46% | |
499 | REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 36 | -0.40 | -1.35 | 0.093 | 0.722 | 1.000 | 2964 | tags=28%, list=14%, signal=32% | |
500 | CYTOSOLIC CALCIUM ION TRANSPORT | 38 | -0.36 | -1.35 | 0.090 | 0.723 | 1.000 | 5630 | tags=42%, list=27%, signal=58% | |
501 | CYCLIC NUCLEOTIDE CATABOLIC PROCESS | 9 | -0.55 | -1.35 | 0.109 | 0.722 | 1.000 | 6175 | tags=56%, list=30%, signal=79% | |
502 | PATTERN SPECIFICATION PROCESS | 387 | -0.29 | -1.35 | 0.060 | 0.723 | 1.000 | 6537 | tags=40%, list=32%, signal=58% | |
503 | POSITIVE REGULATION OF GLOMERULUS DEVELOPMENT | 7 | -0.60 | -1.35 | 0.128 | 0.723 | 1.000 | 6755 | tags=71%, list=33%, signal=106% | |
504 | EMBRYONIC ORGAN MORPHOGENESIS | 290 | -0.30 | -1.35 | 0.062 | 0.724 | 1.000 | 5437 | tags=36%, list=26%, signal=48% | |
505 | ENDODERM FORMATION | 46 | -0.37 | -1.35 | 0.096 | 0.726 | 1.000 | 3799 | tags=30%, list=18%, signal=37% | |
506 | NEGATIVE REGULATION OF LYMPHOCYTE DIFFERENTIATION | 22 | -0.40 | -1.35 | 0.092 | 0.724 | 1.000 | 3650 | tags=36%, list=18%, signal=44% | |
507 | CARDIAC MUSCLE CELL DEVELOPMENT | 39 | -0.36 | -1.35 | 0.108 | 0.723 | 1.000 | 5057 | tags=41%, list=25%, signal=54% | |
508 | SKELETAL MUSCLE SATELLITE CELL DIFFERENTIATION | 5 | -0.67 | -1.35 | 0.123 | 0.724 | 1.000 | 5776 | tags=60%, list=28%, signal=83% | |
509 | GLYCOSPHINGOLIPID CATABOLIC PROCESS | 6 | -0.64 | -1.35 | 0.107 | 0.722 | 1.000 | 1303 | tags=50%, list=6%, signal=53% | |
510 | CERAMIDE CATABOLIC PROCESS | 6 | -0.64 | -1.35 | 0.107 | 0.721 | 1.000 | 1303 | tags=50%, list=6%, signal=53% | |
511 | BONE TRABECULA MORPHOGENESIS | 12 | -0.51 | -1.35 | 0.130 | 0.722 | 1.000 | 3818 | tags=42%, list=19%, signal=51% | |
512 | NEGATIVE REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 18 | -0.48 | -1.35 | 0.142 | 0.723 | 1.000 | 3278 | tags=28%, list=16%, signal=33% | |
513 | SKELETAL MUSCLE CELL DIFFERENTIATION | 50 | -0.40 | -1.35 | 0.101 | 0.723 | 1.000 | 3402 | tags=32%, list=17%, signal=38% | |
514 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 17 | -0.51 | -1.35 | 0.140 | 0.723 | 1.000 | 3278 | tags=29%, list=16%, signal=35% | |
515 | NEGATIVE REGULATION OF GASTRULATION | 5 | -0.65 | -1.35 | 0.135 | 0.722 | 1.000 | 2805 | tags=40%, list=14%, signal=46% | |
516 | NEGATIVE REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 26 | -0.45 | -1.35 | 0.145 | 0.722 | 1.000 | 3000 | tags=31%, list=15%, signal=36% | |
517 | CELL RECOGNITION | 64 | -0.37 | -1.35 | 0.100 | 0.721 | 1.000 | 2307 | tags=28%, list=11%, signal=32% | |
518 | MIDGUT DEVELOPMENT | 6 | -0.62 | -1.35 | 0.156 | 0.720 | 1.000 | 6710 | tags=83%, list=33%, signal=124% | |
519 | CELL-SUBSTRATE JUNCTION ASSEMBLY | 25 | -0.44 | -1.34 | 0.106 | 0.720 | 1.000 | 4566 | tags=48%, list=22%, signal=62% | |
520 | INNER EAR MORPHOGENESIS | 96 | -0.35 | -1.34 | 0.113 | 0.723 | 1.000 | 6442 | tags=47%, list=31%, signal=68% | |
521 | FORELIMB MORPHOGENESIS | 41 | -0.39 | -1.34 | 0.138 | 0.725 | 1.000 | 6504 | tags=54%, list=32%, signal=78% | |
522 | ATRIOVENTRICULAR CANAL DEVELOPMENT | 6 | -0.65 | -1.34 | 0.126 | 0.727 | 1.000 | 1504 | tags=33%, list=7%, signal=36% | |
523 | RESPONSE TO INTERLEUKIN-2 | 5 | -0.67 | -1.34 | 0.139 | 0.726 | 1.000 | 92 | tags=20%, list=0%, signal=20% | |
524 | NEGATIVE REGULATION OF VITAMIN METABOLIC PROCESS | 6 | -0.66 | -1.34 | 0.144 | 0.726 | 1.000 | 1184 | tags=33%, list=6%, signal=35% | |
525 | POSITIVE THYMIC T CELL SELECTION | 11 | -0.52 | -1.34 | 0.127 | 0.726 | 1.000 | 5206 | tags=45%, list=25%, signal=61% | |
526 | CELL FATE DETERMINATION | 38 | -0.38 | -1.34 | 0.133 | 0.727 | 1.000 | 6755 | tags=50%, list=33%, signal=74% | |
527 | REGULATION OF EXCRETION | 5 | -0.71 | -1.34 | 0.128 | 0.726 | 1.000 | 581 | tags=40%, list=3%, signal=41% | |
528 | POSITIVE REGULATION OF CHOLESTEROL ESTERIFICATION | 7 | -0.66 | -1.34 | 0.171 | 0.726 | 1.000 | 5414 | tags=71%, list=26%, signal=97% | |
529 | REGULATION OF EMBRYONIC DEVELOPMENT | 69 | -0.35 | -1.34 | 0.099 | 0.727 | 1.000 | 5050 | tags=36%, list=25%, signal=48% | |
530 | POSITIVE REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 9 | -0.56 | -1.34 | 0.154 | 0.726 | 1.000 | 1504 | tags=33%, list=7%, signal=36% | |
531 | CELLULAR RESPONSE TO COPPER ION | 5 | -0.69 | -1.34 | 0.135 | 0.725 | 1.000 | 3963 | tags=40%, list=19%, signal=50% | |
532 | NEGATIVE REGULATION OF CARDIAC MUSCLE TISSUE GROWTH | 5 | -0.65 | -1.34 | 0.150 | 0.725 | 1.000 | 4163 | tags=60%, list=20%, signal=75% | |
533 | NEGATIVE REGULATION OF HEART GROWTH | 5 | -0.65 | -1.34 | 0.150 | 0.724 | 1.000 | 4163 | tags=60%, list=20%, signal=75% | |
534 | CELL MIGRATION IN HINDBRAIN | 16 | -0.43 | -1.34 | 0.106 | 0.724 | 1.000 | 3356 | tags=38%, list=16%, signal=45% | |
535 | METANEPHRIC DISTAL TUBULE DEVELOPMENT | 5 | -0.66 | -1.34 | 0.110 | 0.724 | 1.000 | 1797 | tags=40%, list=9%, signal=44% | |
536 | SMAD PROTEIN SIGNAL TRANSDUCTION | 16 | -0.49 | -1.34 | 0.114 | 0.724 | 1.000 | 4850 | tags=44%, list=24%, signal=57% | |
537 | NEGATIVE REGULATION OF EPIDERMAL CELL DIFFERENTIATION | 9 | -0.57 | -1.34 | 0.142 | 0.723 | 1.000 | 2781 | tags=44%, list=13%, signal=51% | |
538 | NEGATIVE REGULATION OF FATTY ACID METABOLIC PROCESS | 13 | -0.50 | -1.34 | 0.124 | 0.722 | 1.000 | 3155 | tags=46%, list=15%, signal=54% | |
539 | POSITIVE REGULATION OF CATENIN IMPORT INTO NUCLEUS | 6 | -0.63 | -1.34 | 0.134 | 0.722 | 1.000 | 7038 | tags=83%, list=34%, signal=127% | |
540 | MYOTUBE CELL DEVELOPMENT | 24 | -0.46 | -1.34 | 0.132 | 0.726 | 1.000 | 3360 | tags=38%, list=16%, signal=45% | |
541 | REGULATION OF GLIAL CELL DIFFERENTIATION | 40 | -0.39 | -1.33 | 0.148 | 0.727 | 1.000 | 6996 | tags=48%, list=34%, signal=72% | |
542 | MUSCLE CONTRACTION | 160 | -0.34 | -1.33 | 0.107 | 0.729 | 1.000 | 5405 | tags=39%, list=26%, signal=52% | |
543 | CALCIUM ION TRANSMEMBRANE TRANSPORT | 98 | -0.33 | -1.33 | 0.104 | 0.728 | 1.000 | 6262 | tags=42%, list=30%, signal=60% | |
544 | MUSCLE CELL DEVELOPMENT | 105 | -0.31 | -1.33 | 0.070 | 0.728 | 1.000 | 4823 | tags=33%, list=23%, signal=43% | |
545 | HEMATOPOIETIC STEM CELL DIFFERENTIATION | 11 | -0.48 | -1.33 | 0.125 | 0.729 | 1.000 | 2279 | tags=36%, list=11%, signal=41% | |
546 | POSITIVE REGULATION OF GLUCOSE METABOLIC PROCESS | 18 | -0.42 | -1.33 | 0.118 | 0.728 | 1.000 | 5094 | tags=39%, list=25%, signal=52% | |
547 | GENITALIA DEVELOPMENT | 43 | -0.39 | -1.33 | 0.112 | 0.731 | 1.000 | 4914 | tags=37%, list=24%, signal=49% | |
548 | EMBRYONIC HEART TUBE MORPHOGENESIS | 63 | -0.33 | -1.33 | 0.070 | 0.730 | 1.000 | 3677 | tags=29%, list=18%, signal=35% | |
549 | POSITIVE T CELL SELECTION | 22 | -0.47 | -1.33 | 0.137 | 0.729 | 1.000 | 3046 | tags=32%, list=15%, signal=37% | |
550 | RETINA VASCULATURE MORPHOGENESIS IN CAMERA-TYPE EYE | 11 | -0.51 | -1.33 | 0.169 | 0.728 | 1.000 | 6500 | tags=64%, list=32%, signal=93% | |
551 | MESENCHYMAL TO EPITHELIAL TRANSITION INVOLVED IN METANEPHROS MORPHOGENESIS | 7 | -0.58 | -1.33 | 0.171 | 0.728 | 1.000 | 6755 | tags=71%, list=33%, signal=106% | |
552 | CEREBRAL CORTEX TANGENTIAL MIGRATION | 9 | -0.55 | -1.33 | 0.119 | 0.728 | 1.000 | 1322 | tags=33%, list=6%, signal=36% | |
553 | ENDOCRINE HORMONE SECRETION | 5 | -0.66 | -1.33 | 0.166 | 0.728 | 1.000 | 815 | tags=40%, list=4%, signal=42% | |
554 | CLUSTERING OF VOLTAGE-GATED SODIUM CHANNELS | 5 | -0.65 | -1.33 | 0.158 | 0.730 | 1.000 | 4820 | tags=80%, list=23%, signal=104% | |
555 | CHEMOSENSORY BEHAVIOR | 5 | -0.67 | -1.33 | 0.174 | 0.729 | 1.000 | 5280 | tags=80%, list=26%, signal=108% | |
556 | FATTY ACID TRANSPORT | 37 | -0.39 | -1.33 | 0.104 | 0.729 | 1.000 | 3494 | tags=35%, list=17%, signal=42% | |
557 | POSITIVE REGULATION OF PHOSPHOLIPASE C ACTIVITY | 57 | -0.34 | -1.33 | 0.061 | 0.728 | 1.000 | 6582 | tags=49%, list=32%, signal=72% | |
558 | REGULATION OF PHOSPHOLIPASE C ACTIVITY | 59 | -0.34 | -1.33 | 0.056 | 0.729 | 1.000 | 6582 | tags=49%, list=32%, signal=72% | |
559 | CATECHOLAMINE METABOLIC PROCESS | 15 | -0.51 | -1.33 | 0.166 | 0.731 | 1.000 | 5066 | tags=40%, list=25%, signal=53% | |
560 | CATECHOL-CONTAINING COMPOUND METABOLIC PROCESS | 15 | -0.51 | -1.33 | 0.166 | 0.730 | 1.000 | 5066 | tags=40%, list=25%, signal=53% | |
561 | NEGATIVE REGULATION OF LEUKOCYTE APOPTOTIC PROCESS | 22 | -0.42 | -1.33 | 0.109 | 0.731 | 1.000 | 5601 | tags=41%, list=27%, signal=56% | |
562 | REGULATION OF WATER LOSS VIA SKIN | 15 | -0.47 | -1.33 | 0.152 | 0.732 | 1.000 | 5581 | tags=53%, list=27%, signal=73% | |
563 | ESTABLISHMENT OF SKIN BARRIER | 15 | -0.47 | -1.33 | 0.152 | 0.730 | 1.000 | 5581 | tags=53%, list=27%, signal=73% | |
564 | GLIAL CELL DIFFERENTIATION | 131 | -0.31 | -1.33 | 0.079 | 0.730 | 1.000 | 7035 | tags=43%, list=34%, signal=64% | |
565 | NON-CANONICAL WNT SIGNALING PATHWAY VIA MAPK CASCADE | 5 | -0.62 | -1.33 | 0.157 | 0.729 | 1.000 | 5050 | tags=60%, list=25%, signal=79% | |
566 | MULTICELLULAR ORGANISMAL HOMEOSTASIS | 136 | -0.31 | -1.33 | 0.070 | 0.728 | 1.000 | 4850 | tags=32%, list=24%, signal=42% | |
567 | SMOOTHENED SIGNALING PATHWAY INVOLVED IN DORSAL/VENTRAL NEURAL TUBE PATTERNING | 6 | -0.63 | -1.32 | 0.155 | 0.731 | 1.000 | 5657 | tags=67%, list=27%, signal=92% | |
568 | URETERIC BUD DEVELOPMENT | 70 | -0.34 | -1.32 | 0.108 | 0.732 | 1.000 | 4745 | tags=39%, list=23%, signal=50% | |
569 | POSITIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE/THREONINE KINASE SIGNALING PATHWAY | 54 | -0.35 | -1.32 | 0.107 | 0.734 | 1.000 | 5023 | tags=39%, list=24%, signal=51% | |
570 | REGULATION OF PHOSPHOLIPID BIOSYNTHETIC PROCESS | 8 | -0.55 | -1.32 | 0.138 | 0.742 | 1.000 | 5743 | tags=38%, list=28%, signal=52% | |
571 | POSITIVE REGULATION OF NATURAL KILLER CELL MEDIATED CYTOTOXICITY | 13 | -0.51 | -1.32 | 0.174 | 0.741 | 1.000 | 3208 | tags=31%, list=16%, signal=36% | |
572 | POSITIVE REGULATION OF HORMONE SECRETION | 46 | -0.37 | -1.32 | 0.126 | 0.743 | 1.000 | 3587 | tags=26%, list=17%, signal=32% | |
573 | RESPONSE TO KETONE | 35 | -0.38 | -1.32 | 0.110 | 0.742 | 1.000 | 5990 | tags=37%, list=29%, signal=52% | |
574 | MESODERM MORPHOGENESIS | 65 | -0.33 | -1.32 | 0.115 | 0.743 | 1.000 | 6755 | tags=45%, list=33%, signal=66% | |
575 | NEURON FATE COMMITMENT | 64 | -0.39 | -1.32 | 0.160 | 0.745 | 1.000 | 7178 | tags=48%, list=35%, signal=74% | |
576 | POSITIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 86 | -0.34 | -1.32 | 0.095 | 0.744 | 1.000 | 5814 | tags=37%, list=28%, signal=52% | |
577 | WATER HOMEOSTASIS | 52 | -0.36 | -1.32 | 0.129 | 0.743 | 1.000 | 6031 | tags=42%, list=29%, signal=60% | |
578 | MULTICELLULAR ORGANISMAL WATER HOMEOSTASIS | 52 | -0.36 | -1.32 | 0.129 | 0.742 | 1.000 | 6031 | tags=42%, list=29%, signal=60% | |
579 | T-HELPER 17 CELL LINEAGE COMMITMENT | 5 | -0.72 | -1.32 | 0.181 | 0.741 | 1.000 | 3046 | tags=40%, list=15%, signal=47% | |
580 | REGULATION OF EPIDERMAL GROWTH FACTOR-ACTIVATED RECEPTOR ACTIVITY | 18 | -0.42 | -1.32 | 0.094 | 0.747 | 1.000 | 4264 | tags=44%, list=21%, signal=56% | |
581 | REGULATION OF PROTEIN KINASE B SIGNALING | 74 | -0.34 | -1.32 | 0.069 | 0.746 | 1.000 | 6356 | tags=47%, list=31%, signal=68% | |
582 | PLATELET FORMATION | 18 | -0.46 | -1.32 | 0.123 | 0.747 | 1.000 | 1260 | tags=22%, list=6%, signal=24% | |
583 | SPHINGOMYELIN METABOLIC PROCESS | 5 | -0.67 | -1.31 | 0.126 | 0.747 | 1.000 | 3436 | tags=60%, list=17%, signal=72% | |
584 | PROXIMAL/DISTAL PATTERN FORMATION | 30 | -0.43 | -1.31 | 0.149 | 0.746 | 1.000 | 3815 | tags=43%, list=19%, signal=53% | |
585 | INTERNEURON MIGRATION FROM THE SUBPALLIUM TO THE CORTEX | 9 | -0.56 | -1.31 | 0.183 | 0.749 | 1.000 | 1213 | tags=44%, list=6%, signal=47% | |
586 | PHOSPHATE ION TRANSPORT | 11 | -0.52 | -1.31 | 0.164 | 0.750 | 1.000 | 6039 | tags=45%, list=29%, signal=64% | |
587 | PHOSPHATE ION TRANSMEMBRANE TRANSPORT | 11 | -0.52 | -1.31 | 0.164 | 0.748 | 1.000 | 6039 | tags=45%, list=29%, signal=64% | |
588 | AV NODE CELL TO BUNDLE OF HIS CELL COMMUNICATION | 5 | -0.65 | -1.31 | 0.144 | 0.750 | 1.000 | 5035 | tags=60%, list=24%, signal=79% | |
589 | CELL DIFFERENTIATION IN HINDBRAIN | 23 | -0.43 | -1.31 | 0.138 | 0.751 | 1.000 | 6120 | tags=39%, list=30%, signal=56% | |
590 | FLUID TRANSPORT | 38 | -0.36 | -1.31 | 0.127 | 0.753 | 1.000 | 7501 | tags=53%, list=36%, signal=83% | |
591 | EPITHELIAL CELL MORPHOGENESIS | 48 | -0.34 | -1.31 | 0.124 | 0.752 | 1.000 | 6755 | tags=44%, list=33%, signal=65% | |
592 | MESONEPHRIC TUBULE MORPHOGENESIS | 53 | -0.35 | -1.31 | 0.116 | 0.751 | 1.000 | 4557 | tags=38%, list=22%, signal=48% | |
593 | RESPONSE TO ACTIVITY | 7 | -0.59 | -1.31 | 0.196 | 0.752 | 1.000 | 8391 | tags=100%, list=41%, signal=169% | |
594 | RESPONSE TO MUSCLE ACTIVITY | 7 | -0.59 | -1.31 | 0.196 | 0.751 | 1.000 | 8391 | tags=100%, list=41%, signal=169% | |
595 | LENS DEVELOPMENT IN CAMERA-TYPE EYE | 64 | -0.33 | -1.31 | 0.090 | 0.751 | 1.000 | 6421 | tags=42%, list=31%, signal=61% | |
596 | EMBRYONIC PATTERN SPECIFICATION | 54 | -0.35 | -1.31 | 0.121 | 0.750 | 1.000 | 6710 | tags=48%, list=33%, signal=71% | |
597 | FLOOR PLATE DEVELOPMENT | 8 | -0.58 | -1.31 | 0.172 | 0.749 | 1.000 | 5265 | tags=63%, list=26%, signal=84% | |
598 | REGULATION OF BMP SIGNALING PATHWAY | 40 | -0.36 | -1.31 | 0.120 | 0.749 | 1.000 | 4745 | tags=38%, list=23%, signal=49% | |
599 | CARDIAC CONDUCTION SYSTEM DEVELOPMENT | 13 | -0.48 | -1.31 | 0.159 | 0.750 | 1.000 | 7484 | tags=69%, list=36%, signal=109% | |
600 | POSITIVE REGULATION OF CHOLESTEROL STORAGE | 6 | -0.63 | -1.31 | 0.152 | 0.749 | 1.000 | 5596 | tags=50%, list=27%, signal=69% | |
601 | METANEPHRIC NEPHRON TUBULE DEVELOPMENT | 9 | -0.55 | -1.31 | 0.182 | 0.748 | 1.000 | 2935 | tags=44%, list=14%, signal=52% | |
602 | ENDOCYTIC RECYCLING | 16 | -0.46 | -1.31 | 0.175 | 0.748 | 1.000 | 2259 | tags=38%, list=11%, signal=42% | |
603 | SMOOTH MUSCLE CELL DIFFERENTIATION | 34 | -0.38 | -1.31 | 0.140 | 0.747 | 1.000 | 5287 | tags=47%, list=26%, signal=63% | |
604 | SIGNAL PEPTIDE PROCESSING | 12 | -0.50 | -1.31 | 0.142 | 0.746 | 1.000 | 2822 | tags=42%, list=14%, signal=48% | |
605 | REGULATION OF NITRIC OXIDE BIOSYNTHETIC PROCESS | 27 | -0.42 | -1.31 | 0.126 | 0.746 | 1.000 | 6854 | tags=44%, list=33%, signal=67% | |
606 | ENDOCRINE SYSTEM DEVELOPMENT | 123 | -0.33 | -1.31 | 0.124 | 0.745 | 1.000 | 4850 | tags=33%, list=24%, signal=42% | |
607 | LIPID TRANSPORT | 120 | -0.31 | -1.31 | 0.090 | 0.748 | 1.000 | 3581 | tags=28%, list=17%, signal=34% | |
608 | DERMATAN SULFATE BIOSYNTHETIC PROCESS | 7 | -0.61 | -1.31 | 0.189 | 0.748 | 1.000 | 3258 | tags=43%, list=16%, signal=51% | |
609 | CELLULAR RESPONSE TO KETONE | 21 | -0.40 | -1.31 | 0.146 | 0.747 | 1.000 | 4115 | tags=29%, list=20%, signal=36% | |
610 | OUTER DYNEIN ARM ASSEMBLY | 8 | -0.58 | -1.31 | 0.180 | 0.746 | 1.000 | 5901 | tags=63%, list=29%, signal=88% | |
611 | CHOLESTEROL TRANSPORT | 34 | -0.39 | -1.31 | 0.134 | 0.746 | 1.000 | 3581 | tags=38%, list=17%, signal=46% | |
612 | POSITIVE REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 15 | -0.47 | -1.30 | 0.162 | 0.749 | 1.000 | 1523 | tags=27%, list=7%, signal=29% | |
613 | REGULATION OF CORTICOSTEROID HORMONE SECRETION | 6 | -0.64 | -1.30 | 0.166 | 0.748 | 1.000 | 6961 | tags=83%, list=34%, signal=126% | |
614 | EMBRYONIC SKELETAL JOINT MORPHOGENESIS | 13 | -0.50 | -1.30 | 0.185 | 0.748 | 1.000 | 3799 | tags=38%, list=18%, signal=47% | |
615 | REGULATION OF CARDIAC MUSCLE TISSUE GROWTH | 15 | -0.47 | -1.30 | 0.146 | 0.748 | 1.000 | 6094 | tags=53%, list=30%, signal=76% | |
616 | POSITIVE REGULATION OF CGMP BIOSYNTHETIC PROCESS | 7 | -0.61 | -1.30 | 0.201 | 0.750 | 1.000 | 4575 | tags=57%, list=22%, signal=73% | |
617 | RESPONSE TO MERCURY ION | 5 | -0.63 | -1.30 | 0.175 | 0.751 | 1.000 | 3963 | tags=60%, list=19%, signal=74% | |
618 | STRESS GRANULE ASSEMBLY | 9 | -0.51 | -1.30 | 0.159 | 0.754 | 1.000 | 5399 | tags=33%, list=26%, signal=45% | |
619 | CELL FATE COMMITMENT | 203 | -0.31 | -1.30 | 0.128 | 0.755 | 1.000 | 3951 | tags=28%, list=19%, signal=34% | |
620 | NEGATIVE REGULATION OF PEPTIDYL-TYROSINE PHOSPHORYLATION | 27 | -0.38 | -1.30 | 0.125 | 0.753 | 1.000 | 3630 | tags=33%, list=18%, signal=40% | |
621 | BASE-EXCISION REPAIR, AP SITE FORMATION | 10 | -0.54 | -1.30 | 0.171 | 0.756 | 1.000 | 2575 | tags=40%, list=12%, signal=46% | |
622 | MORPHOGENESIS OF AN ENDOTHELIUM | 15 | -0.46 | -1.30 | 0.172 | 0.757 | 1.000 | 5915 | tags=40%, list=29%, signal=56% | |
623 | ENDOCARDIUM MORPHOGENESIS | 5 | -0.62 | -1.30 | 0.165 | 0.757 | 1.000 | 1376 | tags=40%, list=7%, signal=43% | |
624 | RESPONSE TO LEPTIN | 11 | -0.48 | -1.30 | 0.131 | 0.757 | 1.000 | 4896 | tags=45%, list=24%, signal=60% | |
625 | NEGATIVE REGULATION OF EMBRYONIC DEVELOPMENT | 15 | -0.42 | -1.30 | 0.133 | 0.757 | 1.000 | 4557 | tags=27%, list=22%, signal=34% | |
626 | NEGATIVE REGULATION OF MYOBLAST DIFFERENTIATION | 10 | -0.51 | -1.30 | 0.149 | 0.756 | 1.000 | 3896 | tags=40%, list=19%, signal=49% | |
627 | GAP JUNCTION ASSEMBLY | 6 | -0.63 | -1.30 | 0.157 | 0.756 | 1.000 | 1964 | tags=33%, list=10%, signal=37% | |
628 | STEROL TRANSPORT | 35 | -0.37 | -1.30 | 0.137 | 0.756 | 1.000 | 3581 | tags=37%, list=17%, signal=45% | |
629 | RENAL VESICLE DEVELOPMENT | 13 | -0.47 | -1.30 | 0.158 | 0.757 | 1.000 | 6755 | tags=62%, list=33%, signal=91% | |
630 | REGULATION OF TOOTH MINERALIZATION | 6 | -0.58 | -1.30 | 0.169 | 0.758 | 1.000 | 6188 | tags=83%, list=30%, signal=119% | |
631 | HEART VALVE FORMATION | 13 | -0.48 | -1.30 | 0.149 | 0.756 | 1.000 | 1985 | tags=31%, list=10%, signal=34% | |
632 | NEUROTRANSMITTER UPTAKE | 5 | -0.69 | -1.30 | 0.204 | 0.755 | 1.000 | 3114 | tags=60%, list=15%, signal=71% | |
633 | ORGANIC CATION TRANSPORT | 10 | -0.49 | -1.30 | 0.145 | 0.756 | 1.000 | 6000 | tags=60%, list=29%, signal=85% | |
634 | REGULATION OF TORC1 SIGNALING | 5 | -0.64 | -1.30 | 0.168 | 0.757 | 1.000 | 5902 | tags=60%, list=29%, signal=84% | |
635 | REGULATION OF BRANCHING INVOLVED IN URETERIC BUD MORPHOGENESIS | 14 | -0.48 | -1.29 | 0.174 | 0.759 | 1.000 | 6755 | tags=79%, list=33%, signal=117% | |
636 | NEURAL CREST CELL MIGRATION INVOLVED IN AUTONOMIC NERVOUS SYSTEM DEVELOPMENT | 5 | -0.64 | -1.29 | 0.165 | 0.763 | 1.000 | 2052 | tags=40%, list=10%, signal=44% | |
637 | MAINTENANCE OF GASTROINTESTINAL EPITHELIUM | 7 | -0.59 | -1.29 | 0.167 | 0.764 | 1.000 | 5139 | tags=57%, list=25%, signal=76% | |
638 | MOLTING CYCLE PROCESS | 81 | -0.31 | -1.29 | 0.116 | 0.764 | 1.000 | 4628 | tags=32%, list=22%, signal=41% | |
639 | HAIR CYCLE PROCESS | 81 | -0.31 | -1.29 | 0.116 | 0.763 | 1.000 | 4628 | tags=32%, list=22%, signal=41% | |
640 | CELLULAR RESPONSE TO FATTY ACID | 18 | -0.46 | -1.29 | 0.166 | 0.762 | 1.000 | 3350 | tags=33%, list=16%, signal=40% | |
641 | RENAL TUBULE DEVELOPMENT | 70 | -0.33 | -1.29 | 0.109 | 0.762 | 1.000 | 4557 | tags=36%, list=22%, signal=46% | |
642 | PHOSPHOLIPID CATABOLIC PROCESS | 11 | -0.47 | -1.29 | 0.135 | 0.761 | 1.000 | 1577 | tags=27%, list=8%, signal=30% | |
643 | FOREBRAIN NEURON FATE COMMITMENT | 12 | -0.49 | -1.29 | 0.184 | 0.761 | 1.000 | 743 | tags=17%, list=4%, signal=17% | |
644 | GLUTAMINE FAMILY AMINO ACID BIOSYNTHETIC PROCESS | 8 | -0.54 | -1.29 | 0.177 | 0.760 | 1.000 | 3861 | tags=63%, list=19%, signal=77% | |
645 | SPINAL CORD ASSOCIATION NEURON DIFFERENTIATION | 11 | -0.53 | -1.29 | 0.199 | 0.760 | 1.000 | 925 | tags=18%, list=4%, signal=19% | |
646 | SYNAPSE ASSEMBLY | 58 | -0.35 | -1.29 | 0.151 | 0.759 | 1.000 | 6710 | tags=52%, list=33%, signal=76% | |
647 | REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 146 | -0.29 | -1.29 | 0.072 | 0.759 | 1.000 | 5023 | tags=31%, list=24%, signal=40% | |
648 | GLIAL CELL FATE COMMITMENT | 14 | -0.45 | -1.29 | 0.149 | 0.760 | 1.000 | 6421 | tags=43%, list=31%, signal=62% | |
649 | URETER DEVELOPMENT | 13 | -0.47 | -1.29 | 0.168 | 0.761 | 1.000 | 4557 | tags=54%, list=22%, signal=69% | |
650 | CEREBELLUM DEVELOPMENT | 75 | -0.34 | -1.29 | 0.121 | 0.761 | 1.000 | 6120 | tags=37%, list=30%, signal=53% | |
651 | L-AMINO ACID TRANSPORT | 29 | -0.41 | -1.29 | 0.153 | 0.762 | 1.000 | 2954 | tags=24%, list=14%, signal=28% | |
652 | HEART FORMATION | 12 | -0.47 | -1.29 | 0.151 | 0.761 | 1.000 | 2805 | tags=33%, list=14%, signal=39% | |
653 | POSITIVE REGULATION OF CELL JUNCTION ASSEMBLY | 17 | -0.42 | -1.29 | 0.147 | 0.761 | 1.000 | 8161 | tags=59%, list=40%, signal=97% | |
654 | REGULATION OF LIPOPROTEIN PARTICLE CLEARANCE | 8 | -0.57 | -1.29 | 0.211 | 0.761 | 1.000 | 7617 | tags=75%, list=37%, signal=119% | |
655 | POSITIVE REGULATION OF INTERLEUKIN-17 PRODUCTION | 11 | -0.48 | -1.29 | 0.188 | 0.760 | 1.000 | 4667 | tags=45%, list=23%, signal=59% | |
656 | POSITIVE REGULATION OF VASCULATURE DEVELOPMENT | 83 | -0.31 | -1.29 | 0.066 | 0.760 | 1.000 | 6245 | tags=40%, list=30%, signal=57% | |
657 | POSITIVE REGULATION OF INTERFERON-GAMMA SECRETION | 5 | -0.68 | -1.29 | 0.181 | 0.760 | 1.000 | 5 | tags=20%, list=0%, signal=20% | |
658 | REGULATION OF NAD(P)H OXIDASE ACTIVITY | 5 | -0.59 | -1.29 | 0.185 | 0.761 | 1.000 | 5416 | tags=60%, list=26%, signal=81% | |
659 | REGULATION OF PATHWAY-RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 35 | -0.37 | -1.29 | 0.141 | 0.760 | 1.000 | 4330 | tags=37%, list=21%, signal=47% | |
660 | CELLULAR RESPONSE TO PROSTAGLANDIN E STIMULUS | 7 | -0.58 | -1.29 | 0.179 | 0.760 | 1.000 | 3350 | tags=43%, list=16%, signal=51% | |
661 | REGULATION OF TRANSCRIPTION INVOLVED IN CELL FATE COMMITMENT | 19 | -0.47 | -1.29 | 0.192 | 0.759 | 1.000 | 6996 | tags=47%, list=34%, signal=72% | |
662 | MUSCLE FILAMENT SLIDING | 36 | -0.41 | -1.29 | 0.157 | 0.758 | 1.000 | 4678 | tags=36%, list=23%, signal=47% | |
663 | ACTIN-MYOSIN FILAMENT SLIDING | 36 | -0.41 | -1.29 | 0.157 | 0.757 | 1.000 | 4678 | tags=36%, list=23%, signal=47% | |
664 | SCHWANN CELL DEVELOPMENT | 23 | -0.40 | -1.29 | 0.148 | 0.757 | 1.000 | 471 | tags=13%, list=2%, signal=13% | |
665 | GLYCOSIDE METABOLIC PROCESS | 13 | -0.53 | -1.29 | 0.189 | 0.756 | 1.000 | 4203 | tags=38%, list=20%, signal=48% | |
666 | NEGATIVE REGULATION OF LEUKOCYTE DIFFERENTIATION | 42 | -0.35 | -1.28 | 0.116 | 0.757 | 1.000 | 3937 | tags=33%, list=19%, signal=41% | |
667 | POSITIVE REGULATION OF ENDOTHELIAL CELL MIGRATION | 54 | -0.35 | -1.28 | 0.138 | 0.759 | 1.000 | 7282 | tags=54%, list=35%, signal=83% | |
668 | SUBSTRATE-INDEPENDENT TELENCEPHALIC TANGENTIAL MIGRATION | 10 | -0.53 | -1.28 | 0.200 | 0.758 | 1.000 | 1213 | tags=40%, list=6%, signal=42% | |
669 | SUBSTRATE-INDEPENDENT TELENCEPHALIC TANGENTIAL INTERNEURON MIGRATION | 10 | -0.53 | -1.28 | 0.200 | 0.757 | 1.000 | 1213 | tags=40%, list=6%, signal=42% | |
670 | HYPOTHALAMUS CELL DIFFERENTIATION | 8 | -0.60 | -1.28 | 0.215 | 0.758 | 1.000 | 1322 | tags=25%, list=6%, signal=27% | |
671 | OLIGOSACCHARIDE BIOSYNTHETIC PROCESS | 8 | -0.54 | -1.28 | 0.183 | 0.757 | 1.000 | 1561 | tags=38%, list=8%, signal=41% | |
672 | POSITIVE REGULATION OF PROTEIN KINASE C SIGNALING | 6 | -0.62 | -1.28 | 0.195 | 0.757 | 1.000 | 6710 | tags=83%, list=33%, signal=124% | |
673 | GRANULOCYTE DIFFERENTIATION | 16 | -0.47 | -1.28 | 0.164 | 0.756 | 1.000 | 2121 | tags=31%, list=10%, signal=35% | |
674 | REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE | 44 | -0.40 | -1.28 | 0.136 | 0.755 | 1.000 | 3574 | tags=36%, list=17%, signal=44% | |
675 | NEGATIVE REGULATION OF COAGULATION | 35 | -0.42 | -1.28 | 0.176 | 0.755 | 1.000 | 7097 | tags=54%, list=34%, signal=83% | |
676 | RESPONSE TO STEROL | 14 | -0.45 | -1.28 | 0.156 | 0.754 | 1.000 | 3327 | tags=29%, list=16%, signal=34% | |
677 | SINOATRIAL NODE DEVELOPMENT | 5 | -0.64 | -1.28 | 0.159 | 0.754 | 1.000 | 7484 | tags=100%, list=36%, signal=157% | |
678 | DEVELOPMENTAL CELL GROWTH | 63 | -0.33 | -1.28 | 0.128 | 0.755 | 1.000 | 2679 | tags=25%, list=13%, signal=29% | |
679 | SPECIFICATION OF AXIS POLARITY | 5 | -0.63 | -1.28 | 0.195 | 0.756 | 1.000 | 5465 | tags=80%, list=27%, signal=109% | |
680 | EPIDERMIS DEVELOPMENT | 230 | -0.28 | -1.28 | 0.077 | 0.755 | 1.000 | 4506 | tags=29%, list=22%, signal=37% | |
681 | DIENCEPHALON DEVELOPMENT | 61 | -0.39 | -1.28 | 0.211 | 0.754 | 1.000 | 3815 | tags=28%, list=19%, signal=34% | |
682 | POSITIVE REGULATION OF METANEPHRIC GLOMERULUS DEVELOPMENT | 5 | -0.64 | -1.28 | 0.181 | 0.753 | 1.000 | 2544 | tags=40%, list=12%, signal=46% | |
683 | EAR MORPHOGENESIS | 118 | -0.32 | -1.28 | 0.132 | 0.752 | 1.000 | 6755 | tags=47%, list=33%, signal=70% | |
684 | REGULATION OF CELL FATE COMMITMENT | 12 | -0.51 | -1.28 | 0.193 | 0.753 | 1.000 | 3718 | tags=42%, list=18%, signal=51% | |
685 | RESPIRATORY TUBE DEVELOPMENT | 171 | -0.28 | -1.28 | 0.092 | 0.753 | 1.000 | 4841 | tags=33%, list=23%, signal=42% | |
686 | RETINA DEVELOPMENT IN CAMERA-TYPE EYE | 122 | -0.31 | -1.28 | 0.121 | 0.752 | 1.000 | 7011 | tags=48%, list=34%, signal=73% | |
687 | LUNG-ASSOCIATED MESENCHYME DEVELOPMENT | 10 | -0.48 | -1.28 | 0.176 | 0.751 | 1.000 | 2803 | tags=40%, list=14%, signal=46% | |
688 | REGULATION OF RECEPTOR ACTIVITY | 100 | -0.32 | -1.28 | 0.143 | 0.750 | 1.000 | 4556 | tags=33%, list=22%, signal=42% | |
689 | SUBSTRATE-DEPENDENT CELL MIGRATION | 16 | -0.44 | -1.28 | 0.164 | 0.750 | 1.000 | 1322 | tags=25%, list=6%, signal=27% | |
690 | NEGATIVE REGULATION OF STEM CELL DIFFERENTIATION | 27 | -0.39 | -1.28 | 0.155 | 0.749 | 1.000 | 1797 | tags=26%, list=9%, signal=28% | |
691 | SECONDARY METABOLIC PROCESS | 22 | -0.43 | -1.28 | 0.153 | 0.749 | 1.000 | 5651 | tags=45%, list=27%, signal=63% | |
692 | POSITIVE REGULATION OF NUCLEOTIDE CATABOLIC PROCESS | 11 | -0.47 | -1.28 | 0.185 | 0.748 | 1.000 | 1746 | tags=27%, list=8%, signal=30% | |
693 | NEGATIVE REGULATION OF WOUND HEALING | 39 | -0.38 | -1.28 | 0.162 | 0.749 | 1.000 | 7900 | tags=56%, list=38%, signal=91% | |
694 | CELLULAR GLUCURONIDATION | 12 | -0.45 | -1.28 | 0.182 | 0.751 | 1.000 | 3000 | tags=25%, list=15%, signal=29% | |
695 | NEGATIVE REGULATION OF LIPID BIOSYNTHETIC PROCESS | 27 | -0.40 | -1.28 | 0.144 | 0.750 | 1.000 | 5650 | tags=44%, list=27%, signal=61% | |
696 | CARDIAC MUSCLE FIBER DEVELOPMENT | 6 | -0.60 | -1.28 | 0.205 | 0.749 | 1.000 | 4134 | tags=50%, list=20%, signal=63% | |
697 | NEGATIVE REGULATION OF PROTEIN TYROSINE KINASE ACTIVITY | 14 | -0.45 | -1.28 | 0.159 | 0.749 | 1.000 | 3630 | tags=43%, list=18%, signal=52% | |
698 | BRANCHING INVOLVED IN PROSTATE GLAND MORPHOGENESIS | 13 | -0.49 | -1.28 | 0.185 | 0.747 | 1.000 | 4215 | tags=54%, list=20%, signal=68% | |
699 | EXTRACELLULAR STRUCTURE ORGANIZATION | 275 | -0.33 | -1.28 | 0.144 | 0.747 | 1.000 | 6147 | tags=41%, list=30%, signal=58% | |
700 | REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 18 | -0.40 | -1.28 | 0.145 | 0.748 | 1.000 | 7793 | tags=44%, list=38%, signal=71% | |
701 | EXTRACELLULAR MATRIX ORGANIZATION | 274 | -0.33 | -1.28 | 0.144 | 0.747 | 1.000 | 6147 | tags=41%, list=30%, signal=58% | |
702 | REGULATION OF DENDRITIC CELL ANTIGEN PROCESSING AND PRESENTATION | 5 | -0.63 | -1.28 | 0.200 | 0.747 | 1.000 | 5990 | tags=80%, list=29%, signal=113% | |
703 | POSITIVE REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 14 | -0.45 | -1.28 | 0.186 | 0.748 | 1.000 | 4049 | tags=43%, list=20%, signal=53% | |
704 | POSITIVE REGULATION OF ATP METABOLIC PROCESS | 14 | -0.45 | -1.28 | 0.186 | 0.747 | 1.000 | 4049 | tags=43%, list=20%, signal=53% | |
705 | KIDNEY MORPHOGENESIS | 78 | -0.31 | -1.28 | 0.112 | 0.747 | 1.000 | 4557 | tags=35%, list=22%, signal=44% | |
706 | REGULATION OF SYNAPSE STRUCTURAL PLASTICITY | 5 | -0.66 | -1.28 | 0.186 | 0.746 | 1.000 | 6671 | tags=80%, list=32%, signal=118% | |
707 | ESTABLISHMENT OF APICAL/BASAL CELL POLARITY | 10 | -0.53 | -1.27 | 0.191 | 0.746 | 1.000 | 6740 | tags=70%, list=33%, signal=104% | |
708 | CAMP-MEDIATED SIGNALING | 16 | -0.45 | -1.27 | 0.199 | 0.745 | 1.000 | 3147 | tags=38%, list=15%, signal=44% | |
709 | ENDODERMAL CELL DIFFERENTIATION | 38 | -0.36 | -1.27 | 0.159 | 0.746 | 1.000 | 3677 | tags=32%, list=18%, signal=38% | |
710 | REGULATION OF KIDNEY DEVELOPMENT | 37 | -0.36 | -1.27 | 0.129 | 0.746 | 1.000 | 6988 | tags=62%, list=34%, signal=94% | |
711 | PEPTIDYL-TYROSINE PHOSPHORYLATION | 111 | -0.31 | -1.27 | 0.102 | 0.746 | 1.000 | 5650 | tags=41%, list=27%, signal=56% | |
712 | PEPTIDYL-TYROSINE MODIFICATION | 111 | -0.31 | -1.27 | 0.102 | 0.744 | 1.000 | 5650 | tags=41%, list=27%, signal=56% | |
713 | CEREBRAL CORTEX NEURON DIFFERENTIATION | 21 | -0.44 | -1.27 | 0.186 | 0.744 | 1.000 | 975 | tags=24%, list=5%, signal=25% | |
714 | UV-DAMAGE EXCISION REPAIR | 8 | -0.54 | -1.27 | 0.180 | 0.743 | 1.000 | 2165 | tags=25%, list=11%, signal=28% | |
715 | REGULATION OF HEART CONTRACTION | 161 | -0.33 | -1.27 | 0.147 | 0.742 | 1.000 | 5804 | tags=40%, list=28%, signal=56% | |
716 | POSITIVE REGULATION OF ANGIOGENESIS | 75 | -0.32 | -1.27 | 0.079 | 0.742 | 1.000 | 5480 | tags=35%, list=27%, signal=47% | |
717 | REGULATION OF HORMONE SECRETION | 146 | -0.29 | -1.27 | 0.115 | 0.741 | 1.000 | 3587 | tags=22%, list=17%, signal=26% | |
718 | REGULATION OF PROSTAGLANDIN SECRETION | 5 | -0.64 | -1.27 | 0.222 | 0.740 | 1.000 | 4843 | tags=60%, list=24%, signal=78% | |
719 | SKELETAL SYSTEM DEVELOPMENT | 432 | -0.28 | -1.27 | 0.103 | 0.739 | 1.000 | 4442 | tags=29%, list=22%, signal=36% | |
720 | TELENCEPHALON REGIONALIZATION | 12 | -0.54 | -1.27 | 0.215 | 0.742 | 1.000 | 2851 | tags=42%, list=14%, signal=48% | |
721 | NEGATIVE REGULATION OF G-PROTEIN COUPLED RECEPTOR PROTEIN SIGNALING PATHWAY | 23 | -0.41 | -1.27 | 0.155 | 0.741 | 1.000 | 4140 | tags=30%, list=20%, signal=38% | |
722 | REGULATION OF PEPTIDYL-TYROSINE PHOSPHORYLATION | 141 | -0.31 | -1.27 | 0.110 | 0.741 | 1.000 | 5650 | tags=34%, list=27%, signal=47% | |
723 | CENTRAL NERVOUS SYSTEM NEURON DIFFERENTIATION | 151 | -0.31 | -1.27 | 0.158 | 0.742 | 1.000 | 5587 | tags=32%, list=27%, signal=44% | |
724 | CHLORIDE TRANSPORT | 43 | -0.40 | -1.27 | 0.186 | 0.741 | 1.000 | 6111 | tags=42%, list=30%, signal=59% | |
725 | CEREBELLAR CORTEX MORPHOGENESIS | 33 | -0.37 | -1.27 | 0.160 | 0.740 | 1.000 | 6120 | tags=36%, list=30%, signal=52% | |
726 | BUD ELONGATION INVOLVED IN LUNG BRANCHING | 7 | -0.58 | -1.27 | 0.189 | 0.740 | 1.000 | 3951 | tags=57%, list=19%, signal=71% | |
727 | NEGATIVE REGULATION OF BLOOD COAGULATION | 33 | -0.42 | -1.27 | 0.170 | 0.741 | 1.000 | 7097 | tags=55%, list=34%, signal=83% | |
728 | NEGATIVE REGULATION OF HEMOSTASIS | 33 | -0.42 | -1.27 | 0.170 | 0.740 | 1.000 | 7097 | tags=55%, list=34%, signal=83% | |
729 | DISACCHARIDE METABOLIC PROCESS | 5 | -0.60 | -1.27 | 0.201 | 0.739 | 1.000 | 3018 | tags=40%, list=15%, signal=47% | |
730 | REGULATION OF NON-CANONICAL WNT SIGNALING PATHWAY | 10 | -0.50 | -1.27 | 0.193 | 0.740 | 1.000 | 523 | tags=20%, list=3%, signal=21% | |
731 | MINERALOCORTICOID BIOSYNTHETIC PROCESS | 6 | -0.61 | -1.27 | 0.203 | 0.740 | 1.000 | 8058 | tags=100%, list=39%, signal=164% | |
732 | MINERALOCORTICOID METABOLIC PROCESS | 6 | -0.61 | -1.27 | 0.203 | 0.739 | 1.000 | 8058 | tags=100%, list=39%, signal=164% | |
733 | ENTERIC NERVOUS SYSTEM DEVELOPMENT | 10 | -0.50 | -1.27 | 0.213 | 0.741 | 1.000 | 7305 | tags=80%, list=35%, signal=124% | |
734 | REGULATION OF RESPIRATORY GASEOUS EXCHANGE | 7 | -0.57 | -1.27 | 0.202 | 0.740 | 1.000 | 4392 | tags=43%, list=21%, signal=54% | |
735 | REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 37 | -0.37 | -1.27 | 0.151 | 0.741 | 1.000 | 5743 | tags=38%, list=28%, signal=52% | |
736 | CEREBRAL CORTEX GABAERGIC INTERNEURON DIFFERENTIATION | 11 | -0.56 | -1.27 | 0.233 | 0.741 | 1.000 | 743 | tags=27%, list=4%, signal=28% | |
737 | BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 18 | -0.44 | -1.27 | 0.178 | 0.741 | 1.000 | 2119 | tags=22%, list=10%, signal=25% | |
738 | VERY-LOW-DENSITY LIPOPROTEIN PARTICLE REMODELING | 7 | -0.59 | -1.27 | 0.191 | 0.746 | 1.000 | 3581 | tags=57%, list=17%, signal=69% | |
739 | SOMATOSTATIN RECEPTOR SIGNALING PATHWAY | 5 | -0.72 | -1.27 | 0.186 | 0.746 | 1.000 | 593 | tags=40%, list=3%, signal=41% | |
740 | SOMATOSTATIN SIGNALING PATHWAY | 5 | -0.72 | -1.27 | 0.186 | 0.745 | 1.000 | 593 | tags=40%, list=3%, signal=41% | |
741 | FEMALE PREGNANCY | 87 | -0.32 | -1.26 | 0.124 | 0.745 | 1.000 | 5588 | tags=41%, list=27%, signal=57% | |
742 | REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 67 | -0.32 | -1.26 | 0.130 | 0.746 | 1.000 | 3580 | tags=27%, list=17%, signal=32% | |
743 | IRON ION IMPORT | 7 | -0.52 | -1.26 | 0.194 | 0.748 | 1.000 | 3647 | tags=43%, list=18%, signal=52% | |
744 | CELLULAR RESPONSE TO ACID CHEMICAL | 74 | -0.32 | -1.26 | 0.135 | 0.747 | 1.000 | 2655 | tags=26%, list=13%, signal=29% | |
745 | POSITIVE REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 36 | -0.35 | -1.26 | 0.151 | 0.748 | 1.000 | 4049 | tags=31%, list=20%, signal=38% | |
746 | POSITIVE REGULATION OF GRANULOCYTE DIFFERENTIATION | 6 | -0.56 | -1.26 | 0.204 | 0.748 | 1.000 | 3742 | tags=33%, list=18%, signal=41% | |
747 | ETHANOL METABOLIC PROCESS | 12 | -0.45 | -1.26 | 0.190 | 0.747 | 1.000 | 4632 | tags=42%, list=22%, signal=54% | |
748 | ETHANOL OXIDATION | 12 | -0.45 | -1.26 | 0.190 | 0.746 | 1.000 | 4632 | tags=42%, list=22%, signal=54% | |
749 | REGULATION OF MACROPHAGE DIFFERENTIATION | 13 | -0.49 | -1.26 | 0.166 | 0.745 | 1.000 | 3834 | tags=38%, list=19%, signal=47% | |
750 | REGULATION OF GLUCOCORTICOID SECRETION | 5 | -0.65 | -1.26 | 0.194 | 0.745 | 1.000 | 6561 | tags=80%, list=32%, signal=117% | |
751 | MAMMARY GLAND DEVELOPMENT | 111 | -0.30 | -1.26 | 0.116 | 0.744 | 1.000 | 5050 | tags=34%, list=25%, signal=45% | |
752 | LATERAL SPROUTING FROM AN EPITHELIUM | 9 | -0.51 | -1.26 | 0.192 | 0.744 | 1.000 | 4914 | tags=56%, list=24%, signal=73% | |
753 | OLIGODENDROCYTE DEVELOPMENT | 25 | -0.38 | -1.26 | 0.156 | 0.744 | 1.000 | 7035 | tags=52%, list=34%, signal=79% | |
754 | SMAD PROTEIN IMPORT INTO NUCLEUS | 5 | -0.62 | -1.26 | 0.187 | 0.744 | 1.000 | 3984 | tags=40%, list=19%, signal=50% | |
755 | NEGATIVE REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 5 | -0.65 | -1.26 | 0.213 | 0.744 | 1.000 | 7022 | tags=80%, list=34%, signal=121% | |
756 | PYRIMIDINE DEOXYRIBONUCLEOTIDE METABOLIC PROCESS | 11 | -0.51 | -1.26 | 0.215 | 0.744 | 1.000 | 2575 | tags=45%, list=12%, signal=52% | |
757 | CALCIUM ION IMPORT | 40 | -0.35 | -1.26 | 0.143 | 0.744 | 1.000 | 5637 | tags=43%, list=27%, signal=58% | |
758 | GLIOGENESIS | 153 | -0.29 | -1.26 | 0.111 | 0.745 | 1.000 | 3820 | tags=24%, list=19%, signal=29% | |
759 | POSITIVE REGULATION OF METANEPHROS DEVELOPMENT | 13 | -0.48 | -1.26 | 0.186 | 0.745 | 1.000 | 3849 | tags=46%, list=19%, signal=57% | |
760 | NEUROPEPTIDE SIGNALING PATHWAY | 29 | -0.43 | -1.26 | 0.245 | 0.744 | 1.000 | 6561 | tags=55%, list=32%, signal=81% | |
761 | THYMIC T CELL SELECTION | 23 | -0.44 | -1.26 | 0.183 | 0.744 | 1.000 | 5206 | tags=52%, list=25%, signal=70% | |
762 | PITUITARY GLAND DEVELOPMENT | 35 | -0.39 | -1.26 | 0.216 | 0.744 | 1.000 | 3815 | tags=26%, list=19%, signal=32% | |
763 | NEGATIVE REGULATION OF GLYCOGEN BIOSYNTHETIC PROCESS | 5 | -0.64 | -1.26 | 0.192 | 0.743 | 1.000 | 2938 | tags=60%, list=14%, signal=70% | |
764 | ISOPRENOID METABOLIC PROCESS | 80 | -0.31 | -1.26 | 0.133 | 0.743 | 1.000 | 5414 | tags=36%, list=26%, signal=49% | |
765 | REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 13 | -0.46 | -1.26 | 0.189 | 0.743 | 1.000 | 4163 | tags=38%, list=20%, signal=48% | |
766 | SIGNAL RELEASE | 87 | -0.33 | -1.26 | 0.144 | 0.744 | 1.000 | 3220 | tags=31%, list=16%, signal=37% | |
767 | FLAVIN-CONTAINING COMPOUND METABOLIC PROCESS | 5 | -0.57 | -1.26 | 0.181 | 0.744 | 1.000 | 2938 | tags=40%, list=14%, signal=47% | |
768 | POSITIVE REGULATION OF ERYTHROCYTE DIFFERENTIATION | 11 | -0.47 | -1.26 | 0.148 | 0.744 | 1.000 | 925 | tags=27%, list=4%, signal=29% | |
769 | POSITIVE REGULATION OF STEROID BIOSYNTHETIC PROCESS | 7 | -0.56 | -1.26 | 0.194 | 0.749 | 1.000 | 5050 | tags=43%, list=25%, signal=57% | |
770 | ADRENAL GLAND DEVELOPMENT | 26 | -0.41 | -1.25 | 0.183 | 0.749 | 1.000 | 4090 | tags=38%, list=20%, signal=48% | |
771 | GLUCOCORTICOID BIOSYNTHETIC PROCESS | 9 | -0.57 | -1.25 | 0.233 | 0.749 | 1.000 | 8732 | tags=89%, list=42%, signal=154% | |
772 | NEGATIVE REGULATION OF CARDIAC MUSCLE HYPERTROPHY | 6 | -0.62 | -1.25 | 0.222 | 0.749 | 1.000 | 2622 | tags=33%, list=13%, signal=38% | |
773 | NEGATIVE REGULATION OF MUSCLE HYPERTROPHY | 6 | -0.62 | -1.25 | 0.222 | 0.748 | 1.000 | 2622 | tags=33%, list=13%, signal=38% | |
774 | MUSCLE FIBER DEVELOPMENT | 41 | -0.35 | -1.25 | 0.144 | 0.748 | 1.000 | 3360 | tags=29%, list=16%, signal=35% | |
775 | SCHWANN CELL DIFFERENTIATION | 28 | -0.36 | -1.25 | 0.144 | 0.749 | 1.000 | 4820 | tags=32%, list=23%, signal=42% | |
776 | PEPTIDE HORMONE PROCESSING | 26 | -0.43 | -1.25 | 0.184 | 0.750 | 1.000 | 2650 | tags=31%, list=13%, signal=35% | |
777 | POSITIVE REGULATION OF ODONTOGENESIS | 5 | -0.62 | -1.25 | 0.233 | 0.754 | 1.000 | 6188 | tags=80%, list=30%, signal=114% | |
778 | MYOBLAST DIFFERENTIATION | 28 | -0.38 | -1.25 | 0.186 | 0.754 | 1.000 | 6115 | tags=50%, list=30%, signal=71% | |
779 | TRABECULA FORMATION | 23 | -0.39 | -1.25 | 0.174 | 0.753 | 1.000 | 3797 | tags=35%, list=18%, signal=43% | |
780 | REGULATION OF FEEDING BEHAVIOR | 6 | -0.57 | -1.25 | 0.196 | 0.753 | 1.000 | 2509 | tags=33%, list=12%, signal=38% | |
781 | CHONDROCYTE DIFFERENTIATION INVOLVED IN ENDOCHONDRAL BONE MORPHOGENESIS | 9 | -0.52 | -1.25 | 0.249 | 0.752 | 1.000 | 3732 | tags=33%, list=18%, signal=41% | |
782 | NEUROTRANSMITTER-GATED ION CHANNEL CLUSTERING | 5 | -0.64 | -1.25 | 0.231 | 0.755 | 1.000 | 1860 | tags=40%, list=9%, signal=44% | |
783 | FAT-SOLUBLE VITAMIN METABOLIC PROCESS | 57 | -0.34 | -1.25 | 0.190 | 0.756 | 1.000 | 5572 | tags=39%, list=27%, signal=53% | |
784 | MRNA TRANSCRIPTION | 14 | -0.45 | -1.25 | 0.192 | 0.756 | 1.000 | 4323 | tags=43%, list=21%, signal=54% | |
785 | RESPONSE TO CHOLESTEROL | 12 | -0.45 | -1.25 | 0.160 | 0.756 | 1.000 | 3327 | tags=33%, list=16%, signal=40% | |
786 | FOREBRAIN RADIAL GLIAL CELL DIFFERENTIATION | 5 | -0.60 | -1.25 | 0.217 | 0.755 | 1.000 | 3650 | tags=40%, list=18%, signal=49% | |
787 | ORGANIC HYDROXY COMPOUND TRANSPORT | 87 | -0.31 | -1.25 | 0.104 | 0.755 | 1.000 | 3581 | tags=26%, list=17%, signal=32% | |
788 | REGULATION OF AXONOGENESIS | 119 | -0.29 | -1.25 | 0.102 | 0.755 | 1.000 | 3534 | tags=24%, list=17%, signal=29% | |
789 | HORMONE METABOLIC PROCESS | 91 | -0.32 | -1.25 | 0.167 | 0.755 | 1.000 | 5143 | tags=34%, list=25%, signal=45% | |
790 | REGULATION OF EPIDERMIS DEVELOPMENT | 34 | -0.37 | -1.25 | 0.187 | 0.754 | 1.000 | 2781 | tags=29%, list=13%, signal=34% | |
791 | POSITIVE REGULATION OF INSULIN-LIKE GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 5 | -0.59 | -1.25 | 0.202 | 0.755 | 1.000 | 1746 | tags=40%, list=8%, signal=44% | |
792 | PANCREAS DEVELOPMENT | 68 | -0.31 | -1.25 | 0.149 | 0.755 | 1.000 | 7112 | tags=46%, list=35%, signal=69% | |
793 | NEURON FATE SPECIFICATION | 28 | -0.44 | -1.25 | 0.268 | 0.755 | 1.000 | 6996 | tags=54%, list=34%, signal=81% | |
794 | CHOLESTEROL EFFLUX | 21 | -0.42 | -1.25 | 0.176 | 0.754 | 1.000 | 3581 | tags=43%, list=17%, signal=52% | |
795 | NEGATIVE REGULATION OF DEVELOPMENTAL GROWTH | 45 | -0.35 | -1.25 | 0.156 | 0.754 | 1.000 | 7038 | tags=44%, list=34%, signal=67% | |
796 | SEPTUM PRIMUM DEVELOPMENT | 5 | -0.59 | -1.25 | 0.230 | 0.755 | 1.000 | 1462 | tags=40%, list=7%, signal=43% | |
797 | EXOCRINE SYSTEM DEVELOPMENT | 44 | -0.38 | -1.25 | 0.203 | 0.754 | 1.000 | 4491 | tags=39%, list=22%, signal=49% | |
798 | MYOTUBE DIFFERENTIATION | 50 | -0.37 | -1.25 | 0.195 | 0.754 | 1.000 | 3360 | tags=32%, list=16%, signal=38% | |
799 | TROPHECTODERMAL CELL DIFFERENTIATION | 21 | -0.39 | -1.24 | 0.164 | 0.755 | 1.000 | 3677 | tags=38%, list=18%, signal=46% | |
800 | NEGATIVE REGULATION OF NITRIC OXIDE BIOSYNTHETIC PROCESS | 7 | -0.55 | -1.24 | 0.229 | 0.756 | 1.000 | 4874 | tags=43%, list=24%, signal=56% | |
801 | NEGATIVE REGULATION OF NITRIC OXIDE METABOLIC PROCESS | 7 | -0.55 | -1.24 | 0.229 | 0.755 | 1.000 | 4874 | tags=43%, list=24%, signal=56% | |
802 | NEGATIVE REGULATION OF KERATINOCYTE DIFFERENTIATION | 5 | -0.62 | -1.24 | 0.219 | 0.755 | 1.000 | 2781 | tags=60%, list=13%, signal=69% | |
803 | NEURONAL SIGNAL TRANSDUCTION | 6 | -0.61 | -1.24 | 0.232 | 0.754 | 1.000 | 6120 | tags=67%, list=30%, signal=95% | |
804 | L-ALPHA-AMINO ACID TRANSMEMBRANE TRANSPORT | 24 | -0.41 | -1.24 | 0.183 | 0.757 | 1.000 | 1864 | tags=21%, list=9%, signal=23% | |
805 | POSITIVE REGULATION OF GLIAL CELL DIFFERENTIATION | 21 | -0.42 | -1.24 | 0.228 | 0.759 | 1.000 | 6996 | tags=57%, list=34%, signal=86% | |
806 | URONIC ACID METABOLIC PROCESS | 17 | -0.41 | -1.24 | 0.229 | 0.760 | 1.000 | 3000 | tags=24%, list=15%, signal=28% | |
807 | GLUCURONATE METABOLIC PROCESS | 17 | -0.41 | -1.24 | 0.229 | 0.759 | 1.000 | 3000 | tags=24%, list=15%, signal=28% | |
808 | LONG-CHAIN FATTY ACID TRANSPORT | 30 | -0.40 | -1.24 | 0.178 | 0.758 | 1.000 | 3494 | tags=37%, list=17%, signal=44% | |
809 | POSITIVE REGULATION OF COFACTOR METABOLIC PROCESS | 10 | -0.48 | -1.24 | 0.212 | 0.760 | 1.000 | 1746 | tags=30%, list=8%, signal=33% | |
810 | POSITIVE REGULATION OF COENZYME METABOLIC PROCESS | 10 | -0.48 | -1.24 | 0.212 | 0.759 | 1.000 | 1746 | tags=30%, list=8%, signal=33% | |
811 | THYROID HORMONE METABOLIC PROCESS | 10 | -0.51 | -1.24 | 0.248 | 0.758 | 1.000 | 4455 | tags=40%, list=22%, signal=51% | |
812 | ANION TRANSPORT | 303 | -0.28 | -1.24 | 0.080 | 0.759 | 1.000 | 3676 | tags=25%, list=18%, signal=30% | |
813 | SYMPATHETIC GANGLION DEVELOPMENT | 9 | -0.46 | -1.24 | 0.200 | 0.759 | 1.000 | 2052 | tags=22%, list=10%, signal=25% | |
814 | REGULATION OF DEVELOPMENTAL GROWTH | 138 | -0.30 | -1.24 | 0.183 | 0.758 | 1.000 | 7038 | tags=43%, list=34%, signal=66% | |
815 | KERATINOCYTE DEVELOPMENT | 10 | -0.47 | -1.24 | 0.196 | 0.759 | 1.000 | 1911 | tags=30%, list=9%, signal=33% | |
816 | REGULATION OF GLOMERULUS DEVELOPMENT | 10 | -0.50 | -1.24 | 0.215 | 0.759 | 1.000 | 6988 | tags=70%, list=34%, signal=106% | |
817 | NEGATIVE REGULATION OF FIBRINOLYSIS | 7 | -0.58 | -1.24 | 0.237 | 0.758 | 1.000 | 7097 | tags=71%, list=34%, signal=109% | |
818 | MULTI-MULTICELLULAR ORGANISM PROCESS | 94 | -0.32 | -1.24 | 0.140 | 0.758 | 1.000 | 5588 | tags=40%, list=27%, signal=55% | |
819 | CHONDROITIN SULFATE PROTEOGLYCAN BIOSYNTHETIC PROCESS | 15 | -0.46 | -1.24 | 0.209 | 0.758 | 1.000 | 3927 | tags=47%, list=19%, signal=58% | |
820 | STRIATED MUSCLE CELL DIFFERENTIATION | 149 | -0.29 | -1.24 | 0.129 | 0.758 | 1.000 | 5715 | tags=38%, list=28%, signal=52% | |
821 | SKELETAL SYSTEM MORPHOGENESIS | 206 | -0.29 | -1.24 | 0.168 | 0.758 | 1.000 | 6656 | tags=45%, list=32%, signal=65% | |
822 | POSITIVE REGULATION OF CARDIAC MUSCLE TISSUE GROWTH | 10 | -0.51 | -1.24 | 0.222 | 0.758 | 1.000 | 1504 | tags=30%, list=7%, signal=32% | |
823 | ADENYLATE CYCLASE-ACTIVATING G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 31 | -0.37 | -1.24 | 0.190 | 0.758 | 1.000 | 7840 | tags=58%, list=38%, signal=94% | |
824 | POSITIVE REGULATION OF CORTICOSTEROID HORMONE SECRETION | 5 | -0.63 | -1.24 | 0.228 | 0.758 | 1.000 | 6961 | tags=80%, list=34%, signal=121% | |
825 | GLYCOSAMINOGLYCAN BIOSYNTHETIC PROCESS | 81 | -0.31 | -1.24 | 0.194 | 0.759 | 1.000 | 3463 | tags=25%, list=17%, signal=30% | |
826 | EXCRETION | 31 | -0.41 | -1.24 | 0.255 | 0.759 | 1.000 | 5244 | tags=45%, list=25%, signal=60% | |
827 | NUCLEOSIDE PHOSPHATE CATABOLIC PROCESS | 46 | -0.34 | -1.24 | 0.153 | 0.759 | 1.000 | 4978 | tags=35%, list=24%, signal=46% | |
828 | HINDBRAIN DEVELOPMENT | 118 | -0.29 | -1.24 | 0.136 | 0.758 | 1.000 | 6451 | tags=36%, list=31%, signal=53% | |
829 | BONE DEVELOPMENT | 142 | -0.28 | -1.24 | 0.112 | 0.758 | 1.000 | 5104 | tags=30%, list=25%, signal=40% | |
830 | CARTILAGE DEVELOPMENT INVOLVED IN ENDOCHONDRAL BONE MORPHOGENESIS | 24 | -0.43 | -1.24 | 0.238 | 0.758 | 1.000 | 7586 | tags=63%, list=37%, signal=99% | |
831 | DORSAL/VENTRAL NEURAL TUBE PATTERNING | 19 | -0.41 | -1.24 | 0.157 | 0.757 | 1.000 | 5657 | tags=47%, list=27%, signal=65% | |
832 | EMBRYONIC SKELETAL SYSTEM MORPHOGENESIS | 96 | -0.31 | -1.23 | 0.188 | 0.758 | 1.000 | 6504 | tags=46%, list=32%, signal=67% | |
833 | SOFT PALATE DEVELOPMENT | 5 | -0.59 | -1.23 | 0.195 | 0.758 | 1.000 | 3935 | tags=60%, list=19%, signal=74% | |
834 | TISSUE HOMEOSTASIS | 68 | -0.30 | -1.23 | 0.144 | 0.759 | 1.000 | 5337 | tags=32%, list=26%, signal=44% | |
835 | HEAD MORPHOGENESIS | 36 | -0.35 | -1.23 | 0.160 | 0.759 | 1.000 | 3134 | tags=28%, list=15%, signal=33% | |
836 | REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE BY CIRCULATORY RENIN-ANGIOTENSIN | 15 | -0.46 | -1.23 | 0.214 | 0.759 | 1.000 | 3574 | tags=40%, list=17%, signal=48% | |
837 | POSITIVE REGULATION OF EPIDERMAL CELL DIFFERENTIATION | 11 | -0.44 | -1.23 | 0.219 | 0.758 | 1.000 | 1793 | tags=36%, list=9%, signal=40% | |
838 | BLASTODERM SEGMENTATION | 15 | -0.46 | -1.23 | 0.266 | 0.758 | 1.000 | 6710 | tags=67%, list=33%, signal=99% | |
839 | REGULATION OF ENDOCRINE PROCESS | 21 | -0.41 | -1.23 | 0.223 | 0.758 | 1.000 | 2379 | tags=33%, list=12%, signal=38% | |
840 | NEGATIVE REGULATION BY HOST OF VIRAL TRANSCRIPTION | 10 | -0.52 | -1.23 | 0.232 | 0.758 | 1.000 | 4909 | tags=50%, list=24%, signal=66% | |
841 | NEGATIVE REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 10 | -0.48 | -1.23 | 0.220 | 0.762 | 1.000 | 7691 | tags=60%, list=37%, signal=96% | |
842 | EMBRYONIC ORGAN DEVELOPMENT | 419 | -0.26 | -1.23 | 0.133 | 0.761 | 1.000 | 6451 | tags=39%, list=31%, signal=56% | |
843 | MORPHOGENESIS OF AN EPITHELIAL SHEET | 42 | -0.32 | -1.23 | 0.152 | 0.763 | 1.000 | 3159 | tags=29%, list=15%, signal=34% | |
844 | HOMOPHILIC CELL ADHESION VIA PLASMA MEMBRANE ADHESION MOLECULES | 23 | -0.41 | -1.23 | 0.199 | 0.763 | 1.000 | 3664 | tags=35%, list=18%, signal=42% | |
845 | REGULATION OF AXON EXTENSION | 55 | -0.31 | -1.23 | 0.152 | 0.764 | 1.000 | 2532 | tags=22%, list=12%, signal=25% | |
846 | CELL MIGRATION INVOLVED IN HEART DEVELOPMENT | 14 | -0.47 | -1.23 | 0.230 | 0.765 | 1.000 | 4163 | tags=43%, list=20%, signal=54% | |
847 | AXONEMAL DYNEIN COMPLEX ASSEMBLY | 14 | -0.45 | -1.23 | 0.212 | 0.765 | 1.000 | 5901 | tags=50%, list=29%, signal=70% | |
848 | T CELL SELECTION | 38 | -0.38 | -1.23 | 0.206 | 0.767 | 1.000 | 4746 | tags=39%, list=23%, signal=51% | |
849 | CRANIAL GANGLION DEVELOPMENT | 6 | -0.54 | -1.23 | 0.235 | 0.766 | 1.000 | 6442 | tags=50%, list=31%, signal=73% | |
850 | NEGATIVE REGULATION OF AUTOPHAGY | 32 | -0.34 | -1.23 | 0.161 | 0.766 | 1.000 | 2218 | tags=22%, list=11%, signal=24% | |
851 | REGULATION OF FIBRINOLYSIS | 10 | -0.52 | -1.23 | 0.224 | 0.767 | 1.000 | 7097 | tags=60%, list=34%, signal=91% | |
852 | HAIR FOLLICLE DEVELOPMENT | 80 | -0.30 | -1.23 | 0.160 | 0.766 | 1.000 | 4628 | tags=31%, list=22%, signal=40% | |
853 | AMMONIUM ION METABOLIC PROCESS | 96 | -0.31 | -1.23 | 0.153 | 0.765 | 1.000 | 6630 | tags=42%, list=32%, signal=61% | |
854 | POSITIVE REGULATION OF PEPTIDE SECRETION | 31 | -0.38 | -1.23 | 0.227 | 0.765 | 1.000 | 3587 | tags=26%, list=17%, signal=31% | |
855 | POSITIVE REGULATION OF PEPTIDE HORMONE SECRETION | 31 | -0.38 | -1.23 | 0.227 | 0.765 | 1.000 | 3587 | tags=26%, list=17%, signal=31% | |
856 | RECEPTOR CLUSTERING | 21 | -0.42 | -1.23 | 0.200 | 0.767 | 1.000 | 3170 | tags=29%, list=15%, signal=34% | |
857 | BINDING OF SPERM TO ZONA PELLUCIDA | 12 | -0.46 | -1.23 | 0.248 | 0.766 | 1.000 | 8670 | tags=83%, list=42%, signal=144% | |
858 | LEUKOCYTE APOPTOTIC PROCESS | 9 | -0.50 | -1.22 | 0.241 | 0.767 | 1.000 | 3650 | tags=44%, list=18%, signal=54% | |
859 | VITAMIN METABOLIC PROCESS | 141 | -0.28 | -1.22 | 0.117 | 0.766 | 1.000 | 5740 | tags=36%, list=28%, signal=50% | |
860 | FEMALE GONAD DEVELOPMENT | 68 | -0.29 | -1.22 | 0.135 | 0.765 | 1.000 | 4327 | tags=28%, list=21%, signal=35% | |
861 | REGULATION OF AXON GUIDANCE | 15 | -0.44 | -1.22 | 0.229 | 0.765 | 1.000 | 1322 | tags=27%, list=6%, signal=28% | |
862 | RETINA HOMEOSTASIS | 43 | -0.32 | -1.22 | 0.200 | 0.766 | 1.000 | 4733 | tags=30%, list=23%, signal=39% | |
863 | METENCEPHALON DEVELOPMENT | 86 | -0.31 | -1.22 | 0.174 | 0.765 | 1.000 | 5372 | tags=33%, list=26%, signal=44% | |
864 | ESTABLISHMENT OR MAINTENANCE OF MONOPOLAR CELL POLARITY | 12 | -0.51 | -1.22 | 0.251 | 0.766 | 1.000 | 6740 | tags=67%, list=33%, signal=99% | |
865 | PHASIC SMOOTH MUSCLE CONTRACTION | 8 | -0.52 | -1.22 | 0.247 | 0.765 | 1.000 | 6719 | tags=75%, list=33%, signal=111% | |
866 | SULFATE TRANSPORT | 9 | -0.49 | -1.22 | 0.235 | 0.765 | 1.000 | 152 | tags=22%, list=1%, signal=22% | |
867 | ESTABLISHMENT OF EPITHELIAL CELL APICAL/BASAL POLARITY | 7 | -0.54 | -1.22 | 0.245 | 0.765 | 1.000 | 6710 | tags=71%, list=33%, signal=106% | |
868 | REGULATION OF AUTOPHAGOSOME MATURATION | 5 | -0.59 | -1.22 | 0.214 | 0.765 | 1.000 | 2340 | tags=40%, list=11%, signal=45% | |
869 | ACTIVATION OF PROTEIN KINASE A ACTIVITY | 16 | -0.41 | -1.22 | 0.193 | 0.765 | 1.000 | 8411 | tags=69%, list=41%, signal=116% | |
870 | LIPID LOCALIZATION | 128 | -0.29 | -1.22 | 0.142 | 0.768 | 1.000 | 3581 | tags=27%, list=17%, signal=33% | |
871 | REGULATION OF ESTABLISHMENT OF PLANAR POLARITY | 23 | -0.39 | -1.22 | 0.189 | 0.767 | 1.000 | 3428 | tags=30%, list=17%, signal=36% | |
872 | AMINO ACID TRANSPORT | 78 | -0.32 | -1.22 | 0.155 | 0.768 | 1.000 | 3178 | tags=24%, list=15%, signal=29% | |
873 | RESPONSE TO NUTRIENT | 32 | -0.37 | -1.22 | 0.193 | 0.770 | 1.000 | 2933 | tags=28%, list=14%, signal=33% | |
874 | CAMERA-TYPE EYE DEVELOPMENT | 274 | -0.27 | -1.22 | 0.145 | 0.769 | 1.000 | 7011 | tags=46%, list=34%, signal=69% | |
875 | NEGATIVE REGULATION OF T CELL DIFFERENTIATION IN THYMUS | 7 | -0.50 | -1.22 | 0.230 | 0.769 | 1.000 | 2281 | tags=29%, list=11%, signal=32% | |
876 | NEGATIVE REGULATION OF THYMOCYTE AGGREGATION | 7 | -0.50 | -1.22 | 0.230 | 0.768 | 1.000 | 2281 | tags=29%, list=11%, signal=32% | |
877 | LUNG DEVELOPMENT | 168 | -0.27 | -1.22 | 0.147 | 0.769 | 1.000 | 4841 | tags=32%, list=23%, signal=42% | |
878 | DETERMINATION OF DORSAL/VENTRAL ASYMMETRY | 5 | -0.62 | -1.22 | 0.256 | 0.769 | 1.000 | 4745 | tags=40%, list=23%, signal=52% | |
879 | DETERMINATION OF DORSAL IDENTITY | 5 | -0.62 | -1.22 | 0.256 | 0.768 | 1.000 | 4745 | tags=40%, list=23%, signal=52% | |
880 | ENDOCRINE PANCREAS DEVELOPMENT | 43 | -0.33 | -1.22 | 0.192 | 0.768 | 1.000 | 3327 | tags=23%, list=16%, signal=28% | |
881 | CYCLIC-NUCLEOTIDE-MEDIATED SIGNALING | 21 | -0.40 | -1.22 | 0.234 | 0.768 | 1.000 | 3147 | tags=33%, list=15%, signal=39% | |
882 | HISTONE H3-K4 METHYLATION | 12 | -0.47 | -1.22 | 0.227 | 0.769 | 1.000 | 3839 | tags=42%, list=19%, signal=51% | |
883 | POSITIVE REGULATION OF CILIUM ASSEMBLY | 6 | -0.53 | -1.22 | 0.241 | 0.769 | 1.000 | 9743 | tags=100%, list=47%, signal=190% | |
884 | SKIN EPIDERMIS DEVELOPMENT | 81 | -0.29 | -1.22 | 0.165 | 0.769 | 1.000 | 4628 | tags=31%, list=22%, signal=40% | |
885 | POSITIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 115 | -0.28 | -1.22 | 0.145 | 0.768 | 1.000 | 3580 | tags=23%, list=17%, signal=28% | |
886 | UROGENITAL SYSTEM DEVELOPMENT | 256 | -0.26 | -1.22 | 0.123 | 0.767 | 1.000 | 5437 | tags=35%, list=26%, signal=47% | |
887 | POSITIVE REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 29 | -0.37 | -1.22 | 0.189 | 0.767 | 1.000 | 5743 | tags=41%, list=28%, signal=57% | |
888 | DEVELOPMENT OF PRIMARY FEMALE SEXUAL CHARACTERISTICS | 70 | -0.28 | -1.22 | 0.156 | 0.766 | 1.000 | 4327 | tags=27%, list=21%, signal=34% | |
889 | TONGUE DEVELOPMENT | 17 | -0.43 | -1.22 | 0.236 | 0.766 | 1.000 | 4506 | tags=41%, list=22%, signal=53% | |
890 | INOSITOL PHOSPHATE-MEDIATED SIGNALING | 15 | -0.42 | -1.22 | 0.232 | 0.767 | 1.000 | 3192 | tags=40%, list=15%, signal=47% | |
891 | EYE DEVELOPMENT | 313 | -0.26 | -1.22 | 0.128 | 0.767 | 1.000 | 7011 | tags=46%, list=34%, signal=68% | |
892 | DEOXYRIBONUCLEOTIDE CATABOLIC PROCESS | 17 | -0.47 | -1.22 | 0.252 | 0.767 | 1.000 | 2575 | tags=35%, list=12%, signal=40% | |
893 | DEOXYRIBOSE PHOSPHATE CATABOLIC PROCESS | 17 | -0.47 | -1.22 | 0.252 | 0.766 | 1.000 | 2575 | tags=35%, list=12%, signal=40% | |
894 | EMBRYONIC HEART TUBE DEVELOPMENT | 75 | -0.29 | -1.21 | 0.138 | 0.767 | 1.000 | 3677 | tags=27%, list=18%, signal=32% | |
895 | POSITIVE REGULATION OF GLYCOLYTIC PROCESS | 9 | -0.49 | -1.21 | 0.229 | 0.769 | 1.000 | 1746 | tags=33%, list=8%, signal=36% | |
896 | MACROMOLECULAR COMPLEX REMODELING | 21 | -0.42 | -1.21 | 0.235 | 0.769 | 1.000 | 3581 | tags=38%, list=17%, signal=46% | |
897 | PROTEIN-LIPID COMPLEX REMODELING | 21 | -0.42 | -1.21 | 0.235 | 0.769 | 1.000 | 3581 | tags=38%, list=17%, signal=46% | |
898 | PLASMA LIPOPROTEIN PARTICLE REMODELING | 21 | -0.42 | -1.21 | 0.235 | 0.768 | 1.000 | 3581 | tags=38%, list=17%, signal=46% | |
899 | POSITIVE REGULATION OF NEURON PROJECTION DEVELOPMENT | 145 | -0.28 | -1.21 | 0.142 | 0.770 | 1.000 | 4047 | tags=29%, list=20%, signal=36% | |
900 | NEGATIVE REGULATION OF PEPTIDYL-THREONINE PHOSPHORYLATION | 9 | -0.54 | -1.21 | 0.276 | 0.771 | 1.000 | 4281 | tags=44%, list=21%, signal=56% | |
901 | MAMMARY GLAND MORPHOGENESIS | 50 | -0.33 | -1.21 | 0.202 | 0.770 | 1.000 | 7581 | tags=50%, list=37%, signal=79% | |
902 | RESPONSE TO ISOQUINOLINE ALKALOID | 5 | -0.62 | -1.21 | 0.267 | 0.770 | 1.000 | 3494 | tags=40%, list=17%, signal=48% | |
903 | RESPONSE TO MORPHINE | 5 | -0.62 | -1.21 | 0.267 | 0.770 | 1.000 | 3494 | tags=40%, list=17%, signal=48% | |
904 | REGULATION OF SOMITOGENESIS | 6 | -0.60 | -1.21 | 0.252 | 0.769 | 1.000 | 6831 | tags=67%, list=33%, signal=100% | |
905 | NEGATIVE REGULATION OF GLUCOSE IMPORT | 5 | -0.61 | -1.21 | 0.248 | 0.768 | 1.000 | 4896 | tags=60%, list=24%, signal=79% | |
906 | REGULATION OF FEVER GENERATION | 6 | -0.59 | -1.21 | 0.265 | 0.768 | 1.000 | 3878 | tags=50%, list=19%, signal=62% | |
907 | POSITIVE REGULATION OF FEVER GENERATION | 6 | -0.59 | -1.21 | 0.265 | 0.767 | 1.000 | 3878 | tags=50%, list=19%, signal=62% | |
908 | REGULATION OF HEAT GENERATION | 6 | -0.59 | -1.21 | 0.265 | 0.766 | 1.000 | 3878 | tags=50%, list=19%, signal=62% | |
909 | POSITIVE REGULATION OF HEAT GENERATION | 6 | -0.59 | -1.21 | 0.265 | 0.765 | 1.000 | 3878 | tags=50%, list=19%, signal=62% | |
910 | MUSCLE SYSTEM PROCESS | 180 | -0.30 | -1.21 | 0.192 | 0.765 | 1.000 | 5405 | tags=36%, list=26%, signal=49% | |
911 | POSITIVE REGULATION OF PATHWAY-RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 26 | -0.38 | -1.21 | 0.211 | 0.770 | 1.000 | 4850 | tags=42%, list=24%, signal=55% | |
912 | REGULATION OF MORPHOGENESIS OF A BRANCHING STRUCTURE | 24 | -0.37 | -1.21 | 0.218 | 0.769 | 1.000 | 6755 | tags=58%, list=33%, signal=87% | |
913 | RESPIRATORY SYSTEM DEVELOPMENT | 191 | -0.27 | -1.21 | 0.179 | 0.769 | 1.000 | 4841 | tags=32%, list=23%, signal=42% | |
914 | POSITIVE REGULATION OF NEURON DIFFERENTIATION | 200 | -0.27 | -1.21 | 0.137 | 0.769 | 1.000 | 4047 | tags=28%, list=20%, signal=34% | |
915 | SPHINGOLIPID CATABOLIC PROCESS | 9 | -0.50 | -1.21 | 0.253 | 0.769 | 1.000 | 1577 | tags=44%, list=8%, signal=48% | |
916 | CELLULAR RESPONSE TO LIGHT STIMULUS | 79 | -0.30 | -1.21 | 0.182 | 0.768 | 1.000 | 4833 | tags=30%, list=23%, signal=40% | |
917 | METANEPHRIC NEPHRON EPITHELIUM DEVELOPMENT | 11 | -0.48 | -1.21 | 0.254 | 0.768 | 1.000 | 2935 | tags=36%, list=14%, signal=42% | |
918 | ORGAN FORMATION | 34 | -0.35 | -1.21 | 0.194 | 0.768 | 1.000 | 3815 | tags=35%, list=19%, signal=43% | |
919 | RETINA MORPHOGENESIS IN CAMERA-TYPE EYE | 51 | -0.32 | -1.21 | 0.186 | 0.767 | 1.000 | 5715 | tags=35%, list=28%, signal=49% | |
920 | ENDODERM DEVELOPMENT | 68 | -0.30 | -1.21 | 0.167 | 0.767 | 1.000 | 3799 | tags=26%, list=18%, signal=32% | |
921 | NAD METABOLIC PROCESS | 36 | -0.38 | -1.21 | 0.227 | 0.766 | 1.000 | 4874 | tags=33%, list=24%, signal=44% | |
922 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER INVOLVED IN HEART DEVELOPMENT | 11 | -0.45 | -1.21 | 0.271 | 0.766 | 1.000 | 5430 | tags=45%, list=26%, signal=62% | |
923 | GROWTH | 312 | -0.25 | -1.21 | 0.132 | 0.768 | 1.000 | 6421 | tags=38%, list=31%, signal=55% | |
924 | SODIUM ION TRANSPORT | 68 | -0.33 | -1.21 | 0.223 | 0.768 | 1.000 | 6991 | tags=49%, list=34%, signal=73% | |
925 | POSITIVE REGULATION OF NITRIC OXIDE BIOSYNTHETIC PROCESS | 21 | -0.41 | -1.21 | 0.177 | 0.767 | 1.000 | 6854 | tags=43%, list=33%, signal=64% | |
926 | POSITIVE REGULATION OF NITRIC OXIDE METABOLIC PROCESS | 21 | -0.41 | -1.21 | 0.177 | 0.766 | 1.000 | 6854 | tags=43%, list=33%, signal=64% | |
927 | ACTIVATION OF TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE ACTIVITY | 8 | -0.51 | -1.21 | 0.245 | 0.765 | 1.000 | 6094 | tags=63%, list=30%, signal=89% | |
928 | O-GLYCAN PROCESSING | 50 | -0.35 | -1.21 | 0.216 | 0.765 | 1.000 | 4087 | tags=42%, list=20%, signal=52% | |
929 | NEGATIVE REGULATION OF EPIDERMAL GROWTH FACTOR-ACTIVATED RECEPTOR ACTIVITY | 7 | -0.53 | -1.21 | 0.238 | 0.764 | 1.000 | 3630 | tags=57%, list=18%, signal=69% | |
930 | SYNAPTIC TRANSMISSION | 387 | -0.31 | -1.21 | 0.212 | 0.765 | 1.000 | 6582 | tags=42%, list=32%, signal=61% | |
931 | SYNAPTIC SIGNALING | 387 | -0.31 | -1.21 | 0.212 | 0.764 | 1.000 | 6582 | tags=42%, list=32%, signal=61% | |
932 | TRANS-SYNAPTIC SIGNALING | 387 | -0.31 | -1.21 | 0.212 | 0.763 | 1.000 | 6582 | tags=42%, list=32%, signal=61% | |
933 | SPECIFICATION OF SYMMETRY | 110 | -0.27 | -1.21 | 0.140 | 0.762 | 1.000 | 6779 | tags=40%, list=33%, signal=59% | |
934 | FUNGIFORM PAPILLA DEVELOPMENT | 6 | -0.55 | -1.21 | 0.245 | 0.763 | 1.000 | 6442 | tags=67%, list=31%, signal=97% | |
935 | CELLULAR BIOGENIC AMINE BIOSYNTHETIC PROCESS | 12 | -0.47 | -1.21 | 0.244 | 0.763 | 1.000 | 5852 | tags=42%, list=28%, signal=58% | |
936 | REGULATION OF PROTEIN KINASE A SIGNALING | 9 | -0.47 | -1.21 | 0.226 | 0.763 | 1.000 | 658 | tags=22%, list=3%, signal=23% | |
937 | CEREBELLAR GRANULAR LAYER FORMATION | 9 | -0.54 | -1.20 | 0.270 | 0.762 | 1.000 | 6120 | tags=56%, list=30%, signal=79% | |
938 | CEREBELLAR GRANULE CELL DIFFERENTIATION | 9 | -0.54 | -1.20 | 0.270 | 0.761 | 1.000 | 6120 | tags=56%, list=30%, signal=79% | |
939 | CELLULAR RESPONSE TO NITRIC OXIDE | 8 | -0.49 | -1.20 | 0.219 | 0.761 | 1.000 | 4384 | tags=38%, list=21%, signal=48% | |
940 | CELLULAR RESPONSE TO REACTIVE NITROGEN SPECIES | 8 | -0.49 | -1.20 | 0.219 | 0.760 | 1.000 | 4384 | tags=38%, list=21%, signal=48% | |
941 | ICOSANOID SECRETION | 10 | -0.49 | -1.20 | 0.265 | 0.760 | 1.000 | 4896 | tags=60%, list=24%, signal=79% | |
942 | ICOSANOID TRANSPORT | 10 | -0.49 | -1.20 | 0.265 | 0.759 | 1.000 | 4896 | tags=60%, list=24%, signal=79% | |
943 | FATTY ACID DERIVATIVE TRANSPORT | 10 | -0.49 | -1.20 | 0.265 | 0.759 | 1.000 | 4896 | tags=60%, list=24%, signal=79% | |
944 | CELLULAR RESPONSE TO OSMOTIC STRESS | 11 | -0.45 | -1.20 | 0.208 | 0.759 | 1.000 | 5399 | tags=45%, list=26%, signal=62% | |
945 | POSITIVE REGULATION OF MUSCLE CELL DIFFERENTIATION | 53 | -0.34 | -1.20 | 0.244 | 0.758 | 1.000 | 5715 | tags=47%, list=28%, signal=65% | |
946 | CARNITINE SHUTTLE | 9 | -0.51 | -1.20 | 0.226 | 0.759 | 1.000 | 1103 | tags=33%, list=5%, signal=35% | |
947 | FATTY ACID TRANSMEMBRANE TRANSPORT | 9 | -0.51 | -1.20 | 0.226 | 0.758 | 1.000 | 1103 | tags=33%, list=5%, signal=35% | |
948 | LIPID CATABOLIC PROCESS | 111 | -0.29 | -1.20 | 0.168 | 0.758 | 1.000 | 3595 | tags=28%, list=17%, signal=34% | |
949 | GLUCOSE CATABOLIC PROCESS | 27 | -0.39 | -1.20 | 0.231 | 0.757 | 1.000 | 4394 | tags=30%, list=21%, signal=38% | |
950 | OLIGODENDROCYTE DIFFERENTIATION | 47 | -0.33 | -1.20 | 0.201 | 0.757 | 1.000 | 7035 | tags=47%, list=34%, signal=71% | |
951 | BRANCH ELONGATION INVOLVED IN MAMMARY GLAND DUCT BRANCHING | 5 | -0.60 | -1.20 | 0.267 | 0.759 | 1.000 | 7178 | tags=60%, list=35%, signal=92% | |
952 | CARTILAGE CONDENSATION | 19 | -0.44 | -1.20 | 0.251 | 0.759 | 1.000 | 5311 | tags=47%, list=26%, signal=64% | |
953 | CELL AGGREGATION | 19 | -0.44 | -1.20 | 0.251 | 0.758 | 1.000 | 5311 | tags=47%, list=26%, signal=64% | |
954 | ATRIAL CARDIAC MUSCLE TISSUE DEVELOPMENT | 6 | -0.56 | -1.20 | 0.254 | 0.757 | 1.000 | 4823 | tags=50%, list=23%, signal=65% | |
955 | ATRIAL CARDIAC MUSCLE TISSUE MORPHOGENESIS | 6 | -0.56 | -1.20 | 0.254 | 0.756 | 1.000 | 4823 | tags=50%, list=23%, signal=65% | |
956 | REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 55 | -0.34 | -1.20 | 0.216 | 0.756 | 1.000 | 3534 | tags=27%, list=17%, signal=33% | |
957 | EPITHELIAL CELL MATURATION | 14 | -0.41 | -1.20 | 0.200 | 0.758 | 1.000 | 5743 | tags=50%, list=28%, signal=69% | |
958 | NEGATIVE REGULATION OF RESPONSE TO CYTOKINE STIMULUS | 25 | -0.37 | -1.20 | 0.185 | 0.758 | 1.000 | 3170 | tags=28%, list=15%, signal=33% | |
959 | GLAND MORPHOGENESIS | 113 | -0.29 | -1.20 | 0.193 | 0.758 | 1.000 | 5050 | tags=32%, list=25%, signal=42% | |
960 | FOREBRAIN CELL MIGRATION | 60 | -0.31 | -1.20 | 0.185 | 0.758 | 1.000 | 3650 | tags=27%, list=18%, signal=32% | |
961 | MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 70 | -0.33 | -1.20 | 0.238 | 0.763 | 1.000 | 5912 | tags=47%, list=29%, signal=66% | |
962 | REGULATION OF EXTENT OF CELL GROWTH | 66 | -0.29 | -1.20 | 0.169 | 0.763 | 1.000 | 2653 | tags=20%, list=13%, signal=23% | |
963 | BONE MORPHOGENESIS | 79 | -0.31 | -1.20 | 0.220 | 0.763 | 1.000 | 5104 | tags=35%, list=25%, signal=47% | |
964 | PLASMA LIPOPROTEIN PARTICLE ASSEMBLY | 12 | -0.48 | -1.20 | 0.269 | 0.764 | 1.000 | 3512 | tags=42%, list=17%, signal=50% | |
965 | EYELID DEVELOPMENT IN CAMERA-TYPE EYE | 14 | -0.39 | -1.20 | 0.233 | 0.764 | 1.000 | 6504 | tags=43%, list=32%, signal=63% | |
966 | AMINE BIOSYNTHETIC PROCESS | 13 | -0.45 | -1.20 | 0.246 | 0.763 | 1.000 | 5852 | tags=38%, list=28%, signal=54% | |
967 | OTIC VESICLE DEVELOPMENT | 15 | -0.43 | -1.20 | 0.242 | 0.763 | 1.000 | 4823 | tags=53%, list=23%, signal=70% | |
968 | MITOTIC G2/M TRANSITION CHECKPOINT | 8 | -0.52 | -1.20 | 0.260 | 0.762 | 1.000 | 435 | tags=25%, list=2%, signal=26% | |
969 | EPITHELIAL TUBE BRANCHING INVOLVED IN LUNG MORPHOGENESIS | 27 | -0.35 | -1.20 | 0.208 | 0.762 | 1.000 | 4353 | tags=44%, list=21%, signal=56% | |
970 | SKELETAL MUSCLE FIBER DEVELOPMENT | 20 | -0.42 | -1.20 | 0.254 | 0.761 | 1.000 | 3360 | tags=35%, list=16%, signal=42% | |
971 | EPITHELIAL CILIUM MOVEMENT | 6 | -0.59 | -1.20 | 0.284 | 0.763 | 1.000 | 5186 | tags=50%, list=25%, signal=67% | |
972 | EPITHELIAL CILIUM MOVEMENT INVOLVED IN DETERMINATION OF LEFT/RIGHT ASYMMETRY | 6 | -0.59 | -1.20 | 0.284 | 0.762 | 1.000 | 5186 | tags=50%, list=25%, signal=67% | |
973 | REGULATION OF SYSTEMIC ARTERIAL BLOOD PRESSURE BY RENIN-ANGIOTENSIN | 16 | -0.44 | -1.19 | 0.237 | 0.764 | 1.000 | 3574 | tags=38%, list=17%, signal=45% | |
974 | CARDIAC CELL DEVELOPMENT | 41 | -0.32 | -1.19 | 0.212 | 0.764 | 1.000 | 5057 | tags=39%, list=25%, signal=52% | |
975 | CEREBRAL CORTEX CELL MIGRATION | 45 | -0.32 | -1.19 | 0.193 | 0.763 | 1.000 | 1614 | tags=18%, list=8%, signal=19% | |
976 | REGULATION OF INTERLEUKIN-2 BIOSYNTHETIC PROCESS | 8 | -0.50 | -1.19 | 0.225 | 0.763 | 1.000 | 2493 | tags=38%, list=12%, signal=43% | |
977 | POLARIZED EPITHELIAL CELL DIFFERENTIATION | 9 | -0.48 | -1.19 | 0.252 | 0.763 | 1.000 | 6710 | tags=67%, list=33%, signal=99% | |
978 | POSITIVE REGULATION OF HEMOPOIESIS | 79 | -0.29 | -1.19 | 0.166 | 0.762 | 1.000 | 3742 | tags=27%, list=18%, signal=32% | |
979 | POSITIVE REGULATION OF CALCIUM-MEDIATED SIGNALING | 11 | -0.46 | -1.19 | 0.230 | 0.761 | 1.000 | 1746 | tags=18%, list=8%, signal=20% | |
980 | RESPONSE TO HEXOSE | 40 | -0.31 | -1.19 | 0.192 | 0.761 | 1.000 | 6939 | tags=45%, list=34%, signal=68% | |
981 | RESPONSE TO MONOSACCHARIDE | 40 | -0.31 | -1.19 | 0.192 | 0.760 | 1.000 | 6939 | tags=45%, list=34%, signal=68% | |
982 | METANEPHRIC TUBULE DEVELOPMENT | 11 | -0.48 | -1.19 | 0.289 | 0.761 | 1.000 | 5437 | tags=55%, list=26%, signal=74% | |
983 | NEGATIVE REGULATION OF CELL DIFFERENTIATION | 364 | -0.25 | -1.19 | 0.147 | 0.761 | 1.000 | 4391 | tags=26%, list=21%, signal=32% | |
984 | APPENDAGE MORPHOGENESIS | 140 | -0.28 | -1.19 | 0.179 | 0.761 | 1.000 | 6528 | tags=44%, list=32%, signal=64% | |
985 | LIMB MORPHOGENESIS | 140 | -0.28 | -1.19 | 0.179 | 0.760 | 1.000 | 6528 | tags=44%, list=32%, signal=64% | |
986 | CARDIAC MUSCLE CELL MYOBLAST DIFFERENTIATION | 9 | -0.49 | -1.19 | 0.260 | 0.760 | 1.000 | 6094 | tags=56%, list=30%, signal=79% | |
987 | DETERMINATION OF HEART LEFT/RIGHT ASYMMETRY | 59 | -0.29 | -1.19 | 0.167 | 0.759 | 1.000 | 2805 | tags=22%, list=14%, signal=25% | |
988 | RESPONSE TO ORGANOPHOSPHORUS | 50 | -0.32 | -1.19 | 0.161 | 0.759 | 1.000 | 4628 | tags=34%, list=22%, signal=44% | |
989 | POSITIVE REGULATION OF OXIDATIVE STRESS-INDUCED CELL DEATH | 6 | -0.54 | -1.19 | 0.277 | 0.758 | 1.000 | 7755 | tags=67%, list=38%, signal=107% | |
990 | REGULATION OF SEQUESTERING OF ZINC ION | 5 | -0.57 | -1.19 | 0.262 | 0.758 | 1.000 | 7944 | tags=80%, list=39%, signal=130% | |
991 | ORGANIC ANION TRANSPORT | 242 | -0.27 | -1.19 | 0.147 | 0.757 | 1.000 | 3625 | tags=25%, list=18%, signal=30% | |
992 | REGULATION OF METANEPHROS DEVELOPMENT | 15 | -0.44 | -1.19 | 0.243 | 0.757 | 1.000 | 3849 | tags=47%, list=19%, signal=57% | |
993 | SKELETAL MYOFIBRIL ASSEMBLY | 8 | -0.55 | -1.19 | 0.273 | 0.757 | 1.000 | 4823 | tags=38%, list=23%, signal=49% | |
994 | REGULATION OF PHOTORECEPTOR CELL DIFFERENTIATION | 5 | -0.60 | -1.19 | 0.262 | 0.758 | 1.000 | 3718 | tags=40%, list=18%, signal=49% | |
995 | NEGATIVE REGULATION OF PHOTORECEPTOR CELL DIFFERENTIATION | 5 | -0.60 | -1.19 | 0.262 | 0.757 | 1.000 | 3718 | tags=40%, list=18%, signal=49% | |
996 | RHYTHMIC PROCESS | 132 | -0.26 | -1.19 | 0.134 | 0.757 | 1.000 | 4327 | tags=27%, list=21%, signal=34% | |
997 | POSITIVE REGULATION OF ADHERENS JUNCTION ORGANIZATION | 14 | -0.40 | -1.19 | 0.240 | 0.756 | 1.000 | 8841 | tags=64%, list=43%, signal=113% | |
998 | CELL GROWTH | 83 | -0.29 | -1.19 | 0.202 | 0.756 | 1.000 | 7047 | tags=48%, list=34%, signal=73% | |
999 | FIBRINOLYSIS | 14 | -0.48 | -1.19 | 0.259 | 0.757 | 1.000 | 7097 | tags=71%, list=34%, signal=109% | |
1000 | NEGATIVE REGULATION OF CALCIUM ION TRANSPORT INTO CYTOSOL | 12 | -0.42 | -1.19 | 0.251 | 0.757 | 1.000 | 2053 | tags=17%, list=10%, signal=19% | |
1001 | MESENCHYMAL TO EPITHELIAL TRANSITION | 14 | -0.43 | -1.19 | 0.276 | 0.758 | 1.000 | 6755 | tags=57%, list=33%, signal=85% | |
1002 | REGULATION OF GLUTAMATE RECEPTOR SIGNALING PATHWAY | 24 | -0.43 | -1.19 | 0.284 | 0.757 | 1.000 | 6238 | tags=54%, list=30%, signal=78% | |
1003 | GLYCOLIPID CATABOLIC PROCESS | 8 | -0.53 | -1.19 | 0.290 | 0.758 | 1.000 | 1303 | tags=38%, list=6%, signal=40% | |
1004 | DETECTION OF STIMULUS | 211 | -0.27 | -1.19 | 0.196 | 0.758 | 1.000 | 5485 | tags=32%, list=27%, signal=43% | |
1005 | SMOOTH MUSCLE TISSUE DEVELOPMENT | 23 | -0.37 | -1.19 | 0.228 | 0.758 | 1.000 | 3849 | tags=39%, list=19%, signal=48% | |
1006 | CANONICAL WNT SIGNALING PATHWAY | 47 | -0.32 | -1.19 | 0.192 | 0.758 | 1.000 | 5600 | tags=43%, list=27%, signal=58% | |
1007 | REGULATION OF PLASMINOGEN ACTIVATION | 8 | -0.53 | -1.19 | 0.250 | 0.758 | 1.000 | 7097 | tags=75%, list=34%, signal=114% | |
1008 | POSITIVE REGULATION OF RECEPTOR RECYCLING | 7 | -0.49 | -1.19 | 0.275 | 0.758 | 1.000 | 4148 | tags=57%, list=20%, signal=72% | |
1009 | DEVELOPMENTAL GROWTH | 293 | -0.25 | -1.19 | 0.148 | 0.757 | 1.000 | 5642 | tags=33%, list=27%, signal=45% | |
1010 | REGULATION OF ACTIN CYTOSKELETON ORGANIZATION | 152 | -0.27 | -1.19 | 0.173 | 0.762 | 1.000 | 2964 | tags=23%, list=14%, signal=27% | |
1011 | SPONGIOTROPHOBLAST DIFFERENTIATION | 5 | -0.56 | -1.19 | 0.262 | 0.762 | 1.000 | 3580 | tags=60%, list=17%, signal=73% | |
1012 | POSITIVE REGULATION OF MYELOID CELL DIFFERENTIATION | 41 | -0.31 | -1.19 | 0.187 | 0.761 | 1.000 | 4330 | tags=27%, list=21%, signal=34% | |
1013 | CEREBELLAR CORTEX DEVELOPMENT | 47 | -0.33 | -1.19 | 0.218 | 0.761 | 1.000 | 6120 | tags=36%, list=30%, signal=51% | |
1014 | PLASMA LIPOPROTEIN PARTICLE ORGANIZATION | 26 | -0.39 | -1.19 | 0.235 | 0.760 | 1.000 | 3581 | tags=35%, list=17%, signal=42% | |
1015 | REGULATION OF HORMONE METABOLIC PROCESS | 15 | -0.43 | -1.19 | 0.248 | 0.761 | 1.000 | 5050 | tags=47%, list=25%, signal=62% | |
1016 | POSITIVE REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 11 | -0.45 | -1.19 | 0.262 | 0.760 | 1.000 | 8342 | tags=73%, list=40%, signal=122% | |
1017 | REGULATION OF TOLERANCE INDUCTION | 10 | -0.47 | -1.19 | 0.276 | 0.760 | 1.000 | 2493 | tags=30%, list=12%, signal=34% | |
1018 | POSITIVE REGULATION OF PHOSPHATIDYLINOSITOL 3-KINASE ACTIVITY | 20 | -0.41 | -1.18 | 0.252 | 0.761 | 1.000 | 5650 | tags=50%, list=27%, signal=69% | |
1019 | CONNECTIVE TISSUE DEVELOPMENT | 177 | -0.28 | -1.18 | 0.221 | 0.761 | 1.000 | 5743 | tags=36%, list=28%, signal=49% | |
1020 | NEUROBLAST PROLIFERATION | 28 | -0.35 | -1.18 | 0.191 | 0.760 | 1.000 | 5688 | tags=43%, list=28%, signal=59% | |
1021 | HINDLIMB MORPHOGENESIS | 38 | -0.34 | -1.18 | 0.254 | 0.761 | 1.000 | 4206 | tags=29%, list=20%, signal=36% | |
1022 | SPROUTING ANGIOGENESIS | 39 | -0.34 | -1.18 | 0.229 | 0.763 | 1.000 | 7204 | tags=46%, list=35%, signal=71% | |
1023 | REGULATION OF PROTEIN IMPORT INTO NUCLEUS, TRANSLOCATION | 7 | -0.49 | -1.18 | 0.224 | 0.764 | 1.000 | 4951 | tags=57%, list=24%, signal=75% | |
1024 | SEMAPHORIN-PLEXIN SIGNALING PATHWAY INVOLVED IN NEURON PROJECTION GUIDANCE | 5 | -0.58 | -1.18 | 0.287 | 0.765 | 1.000 | 6400 | tags=60%, list=31%, signal=87% | |
1025 | LIMB BUD FORMATION | 6 | -0.55 | -1.18 | 0.254 | 0.767 | 1.000 | 3815 | tags=50%, list=19%, signal=61% | |
1026 | REGULATION OF GASTRULATION | 22 | -0.35 | -1.18 | 0.252 | 0.766 | 1.000 | 2805 | tags=27%, list=14%, signal=32% | |
1027 | PURINE NUCLEOTIDE CATABOLIC PROCESS | 31 | -0.35 | -1.18 | 0.243 | 0.768 | 1.000 | 6511 | tags=45%, list=32%, signal=66% | |
1028 | CARDIAC MUSCLE CELL DIFFERENTIATION | 64 | -0.29 | -1.18 | 0.205 | 0.768 | 1.000 | 5582 | tags=41%, list=27%, signal=56% | |
1029 | SENSORY ORGAN DEVELOPMENT | 483 | -0.25 | -1.18 | 0.194 | 0.768 | 1.000 | 6528 | tags=40%, list=32%, signal=57% | |
1030 | DIVALENT METAL ION TRANSPORT | 148 | -0.28 | -1.18 | 0.196 | 0.768 | 1.000 | 5804 | tags=36%, list=28%, signal=50% | |
1031 | LENS FIBER CELL DIFFERENTIATION | 26 | -0.38 | -1.18 | 0.235 | 0.767 | 1.000 | 6421 | tags=50%, list=31%, signal=73% | |
1032 | ANATOMICAL STRUCTURE REGRESSION | 9 | -0.49 | -1.18 | 0.269 | 0.768 | 1.000 | 3031 | tags=33%, list=15%, signal=39% | |
1033 | CELL-MATRIX ADHESION | 64 | -0.31 | -1.18 | 0.211 | 0.767 | 1.000 | 4566 | tags=36%, list=22%, signal=46% | |
1034 | ESTABLISHMENT OF MONOPOLAR CELL POLARITY | 11 | -0.49 | -1.18 | 0.296 | 0.767 | 1.000 | 8654 | tags=82%, list=42%, signal=141% | |
1035 | REGULATION OF DENDRITE EXTENSION | 15 | -0.41 | -1.18 | 0.318 | 0.767 | 1.000 | 6395 | tags=53%, list=31%, signal=77% | |
1036 | POSITIVE REGULATION OF DENDRITE EXTENSION | 15 | -0.41 | -1.18 | 0.318 | 0.766 | 1.000 | 6395 | tags=53%, list=31%, signal=77% | |
1037 | NEGATIVE REGULATION OF DEVELOPMENTAL PROCESS | 481 | -0.24 | -1.18 | 0.167 | 0.766 | 1.000 | 4391 | tags=25%, list=21%, signal=31% | |
1038 | CARTILAGE DEVELOPMENT | 130 | -0.29 | -1.18 | 0.236 | 0.766 | 1.000 | 4835 | tags=32%, list=23%, signal=41% | |
1039 | REGULATION OF HORMONE LEVELS | 268 | -0.26 | -1.18 | 0.170 | 0.765 | 1.000 | 6598 | tags=37%, list=32%, signal=54% | |
1040 | POSITIVE REGULATION OF LEUKOCYTE DIFFERENTIATION | 62 | -0.29 | -1.18 | 0.193 | 0.764 | 1.000 | 3742 | tags=27%, list=18%, signal=33% | |
1041 | ADHERENS JUNCTION ORGANIZATION | 51 | -0.34 | -1.18 | 0.239 | 0.764 | 1.000 | 4680 | tags=33%, list=23%, signal=43% | |
1042 | TELENCEPHALON CELL MIGRATION | 57 | -0.31 | -1.18 | 0.208 | 0.764 | 1.000 | 3650 | tags=26%, list=18%, signal=32% | |
1043 | CELL FATE COMMITMENT INVOLVED IN FORMATION OF PRIMARY GERM LAYER | 25 | -0.35 | -1.18 | 0.243 | 0.764 | 1.000 | 4380 | tags=36%, list=21%, signal=46% | |
1044 | MAMMARY GLAND ALVEOLUS DEVELOPMENT | 20 | -0.40 | -1.18 | 0.266 | 0.766 | 1.000 | 5010 | tags=45%, list=24%, signal=59% | |
1045 | MAMMARY GLAND LOBULE DEVELOPMENT | 20 | -0.40 | -1.18 | 0.266 | 0.765 | 1.000 | 5010 | tags=45%, list=24%, signal=59% | |
1046 | EMBRYONIC RETINA MORPHOGENESIS IN CAMERA-TYPE EYE | 7 | -0.52 | -1.18 | 0.257 | 0.765 | 1.000 | 5715 | tags=43%, list=28%, signal=59% | |
1047 | SULFATION | 11 | -0.48 | -1.18 | 0.297 | 0.765 | 1.000 | 4303 | tags=36%, list=21%, signal=46% | |
1048 | FEMALE SEX DIFFERENTIATION | 81 | -0.27 | -1.18 | 0.187 | 0.766 | 1.000 | 4327 | tags=26%, list=21%, signal=33% | |
1049 | MULTICELLULAR ORGANISMAL SIGNALING | 126 | -0.30 | -1.18 | 0.243 | 0.766 | 1.000 | 5804 | tags=40%, list=28%, signal=56% | |
1050 | TRNA METHYLATION | 5 | -0.65 | -1.18 | 0.334 | 0.765 | 1.000 | 1217 | tags=20%, list=6%, signal=21% | |
1051 | NEURAL RETINA DEVELOPMENT | 46 | -0.32 | -1.17 | 0.227 | 0.766 | 1.000 | 7002 | tags=43%, list=34%, signal=66% | |
1052 | SYNAPSE ORGANIZATION | 81 | -0.30 | -1.17 | 0.240 | 0.766 | 1.000 | 6710 | tags=47%, list=33%, signal=69% | |
1053 | MORPHOGENESIS OF A BRANCHING EPITHELIUM | 178 | -0.26 | -1.17 | 0.209 | 0.769 | 1.000 | 4914 | tags=30%, list=24%, signal=39% | |
1054 | EMBRYONIC LIMB MORPHOGENESIS | 122 | -0.27 | -1.17 | 0.212 | 0.771 | 1.000 | 6504 | tags=43%, list=32%, signal=63% | |
1055 | EMBRYONIC APPENDAGE MORPHOGENESIS | 122 | -0.27 | -1.17 | 0.212 | 0.770 | 1.000 | 6504 | tags=43%, list=32%, signal=63% | |
1056 | CELLULAR RESPONSE TO VASCULAR ENDOTHELIAL GROWTH FACTOR STIMULUS | 25 | -0.42 | -1.17 | 0.256 | 0.770 | 1.000 | 5915 | tags=48%, list=29%, signal=67% | |
1057 | REGULATION OF MESONEPHROS DEVELOPMENT | 17 | -0.40 | -1.17 | 0.257 | 0.770 | 1.000 | 6755 | tags=71%, list=33%, signal=105% | |
1058 | REGULATION OF MUSCLE ADAPTATION | 29 | -0.36 | -1.17 | 0.278 | 0.770 | 1.000 | 7292 | tags=45%, list=35%, signal=69% | |
1059 | NEGATIVE REGULATION OF EPITHELIAL CELL MIGRATION | 45 | -0.31 | -1.17 | 0.233 | 0.771 | 1.000 | 2061 | tags=20%, list=10%, signal=22% | |
1060 | CELLULAR RESPONSE TO ATP | 9 | -0.48 | -1.17 | 0.284 | 0.770 | 1.000 | 4628 | tags=44%, list=22%, signal=57% | |
1061 | AMINOGLYCAN BIOSYNTHETIC PROCESS | 82 | -0.30 | -1.17 | 0.244 | 0.770 | 1.000 | 3463 | tags=24%, list=17%, signal=29% | |
1062 | FORMATION OF ANATOMICAL BOUNDARY | 5 | -0.57 | -1.17 | 0.313 | 0.769 | 1.000 | 3677 | tags=60%, list=18%, signal=73% | |
1063 | NUCLEOTIDE CATABOLIC PROCESS | 43 | -0.32 | -1.17 | 0.194 | 0.769 | 1.000 | 6511 | tags=42%, list=32%, signal=61% | |
1064 | CHLORIDE TRANSMEMBRANE TRANSPORT | 41 | -0.36 | -1.17 | 0.288 | 0.769 | 1.000 | 6111 | tags=39%, list=30%, signal=55% | |
1065 | NEGATIVE REGULATION OF RECEPTOR ACTIVITY | 28 | -0.35 | -1.17 | 0.244 | 0.769 | 1.000 | 4352 | tags=29%, list=21%, signal=36% | |
1066 | INTRACELLULAR ESTROGEN RECEPTOR SIGNALING PATHWAY | 8 | -0.44 | -1.17 | 0.262 | 0.771 | 1.000 | 6050 | tags=63%, list=29%, signal=88% | |
1067 | MESODERMAL CELL FATE SPECIFICATION | 7 | -0.53 | -1.17 | 0.289 | 0.770 | 1.000 | 7789 | tags=86%, list=38%, signal=138% | |
1068 | REGULATION OF SYSTEM PROCESS | 277 | -0.29 | -1.17 | 0.238 | 0.771 | 1.000 | 5804 | tags=37%, list=28%, signal=51% | |
1069 | TRIGEMINAL NERVE DEVELOPMENT | 7 | -0.51 | -1.17 | 0.296 | 0.771 | 1.000 | 6400 | tags=57%, list=31%, signal=83% | |
1070 | REGULATION OF LYMPHOCYTE CHEMOTAXIS | 15 | -0.45 | -1.17 | 0.285 | 0.772 | 1.000 | 26 | tags=13%, list=0%, signal=13% | |
1071 | CATION TRANSMEMBRANE TRANSPORT | 351 | -0.27 | -1.17 | 0.199 | 0.771 | 1.000 | 6086 | tags=36%, list=30%, signal=50% | |
1072 | SKIN DEVELOPMENT | 178 | -0.26 | -1.17 | 0.200 | 0.773 | 1.000 | 4628 | tags=28%, list=22%, signal=36% | |
1073 | DETERMINATION OF BILATERAL SYMMETRY | 109 | -0.26 | -1.17 | 0.192 | 0.773 | 1.000 | 6779 | tags=39%, list=33%, signal=58% | |
1074 | REGULATION OF STEROID HORMONE SECRETION | 8 | -0.52 | -1.17 | 0.307 | 0.773 | 1.000 | 1825 | tags=38%, list=9%, signal=41% | |
1075 | REGULATION OF STEROID BIOSYNTHETIC PROCESS | 27 | -0.36 | -1.17 | 0.243 | 0.773 | 1.000 | 5050 | tags=33%, list=25%, signal=44% | |
1076 | DEVELOPMENTAL MATURATION | 179 | -0.26 | -1.17 | 0.220 | 0.772 | 1.000 | 5743 | tags=36%, list=28%, signal=50% | |
1077 | NEPHRON TUBULE FORMATION | 14 | -0.41 | -1.17 | 0.275 | 0.771 | 1.000 | 6755 | tags=64%, list=33%, signal=96% | |
1078 | SEX DIFFERENTIATION | 195 | -0.25 | -1.17 | 0.176 | 0.771 | 1.000 | 5621 | tags=32%, list=27%, signal=44% | |
1079 | BEHAVIORAL RESPONSE TO NICOTINE | 5 | -0.58 | -1.17 | 0.302 | 0.770 | 1.000 | 4097 | tags=40%, list=20%, signal=50% | |
1080 | RENAL SYSTEM DEVELOPMENT | 220 | -0.25 | -1.17 | 0.165 | 0.770 | 1.000 | 5437 | tags=34%, list=26%, signal=46% | |
1081 | HEART TRABECULA FORMATION | 14 | -0.42 | -1.17 | 0.280 | 0.771 | 1.000 | 2964 | tags=29%, list=14%, signal=33% | |
1082 | NEURONAL ION CHANNEL CLUSTERING | 9 | -0.50 | -1.17 | 0.316 | 0.771 | 1.000 | 4820 | tags=56%, list=23%, signal=72% | |
1083 | NEGATIVE REGULATION OF TRANSCRIPTION REGULATORY REGION DNA BINDING | 11 | -0.45 | -1.17 | 0.256 | 0.771 | 1.000 | 740 | tags=18%, list=4%, signal=19% | |
1084 | POSITIVE REGULATION OF HORMONE METABOLIC PROCESS | 7 | -0.51 | -1.16 | 0.266 | 0.771 | 1.000 | 5050 | tags=71%, list=25%, signal=95% | |
1085 | COMMITMENT OF NEURONAL CELL TO SPECIFIC NEURON TYPE IN FOREBRAIN | 7 | -0.52 | -1.16 | 0.263 | 0.771 | 1.000 | 42 | tags=14%, list=0%, signal=14% | |
1086 | CGMP-MEDIATED SIGNALING | 6 | -0.55 | -1.16 | 0.283 | 0.770 | 1.000 | 2825 | tags=50%, list=14%, signal=58% | |
1087 | PROTEIN HETEROTETRAMERIZATION | 10 | -0.46 | -1.16 | 0.284 | 0.770 | 1.000 | 6147 | tags=50%, list=30%, signal=71% | |
1088 | SPECIFICATION OF ORGAN IDENTITY | 14 | -0.42 | -1.16 | 0.268 | 0.770 | 1.000 | 3815 | tags=43%, list=19%, signal=53% | |
1089 | RESPONSE TO PURINE-CONTAINING COMPOUND | 52 | -0.30 | -1.16 | 0.199 | 0.770 | 1.000 | 4628 | tags=31%, list=22%, signal=40% | |
1090 | SERINE FAMILY AMINO ACID CATABOLIC PROCESS | 6 | -0.56 | -1.16 | 0.274 | 0.771 | 1.000 | 6895 | tags=67%, list=33%, signal=100% | |
1091 | ADENYLATE CYCLASE-MODULATING G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 77 | -0.31 | -1.16 | 0.263 | 0.770 | 1.000 | 5983 | tags=38%, list=29%, signal=53% | |
1092 | REGULATION OF DOPAMINE SECRETION | 8 | -0.51 | -1.16 | 0.313 | 0.771 | 1.000 | 9352 | tags=75%, list=45%, signal=137% | |
1093 | RETINA VASCULATURE DEVELOPMENT IN CAMERA-TYPE EYE | 19 | -0.41 | -1.16 | 0.296 | 0.771 | 1.000 | 6500 | tags=63%, list=32%, signal=92% | |
1094 | PHOSPHATE ION HOMEOSTASIS | 9 | -0.47 | -1.16 | 0.304 | 0.770 | 1.000 | 6270 | tags=56%, list=30%, signal=80% | |
1095 | TRIVALENT INORGANIC ANION HOMEOSTASIS | 9 | -0.47 | -1.16 | 0.304 | 0.769 | 1.000 | 6270 | tags=56%, list=30%, signal=80% | |
1096 | SODIUM ION TRANSMEMBRANE TRANSPORT | 66 | -0.33 | -1.16 | 0.271 | 0.770 | 1.000 | 6852 | tags=47%, list=33%, signal=70% | |
1097 | REGULATION OF CATECHOLAMINE SECRETION | 16 | -0.43 | -1.16 | 0.303 | 0.770 | 1.000 | 160 | tags=13%, list=1%, signal=13% | |
1098 | MORPHOGENESIS OF AN EPITHELIUM | 428 | -0.23 | -1.16 | 0.158 | 0.770 | 1.000 | 4923 | tags=28%, list=24%, signal=36% | |
1099 | NEGATIVE REGULATION OF HEART CONTRACTION | 10 | -0.46 | -1.16 | 0.293 | 0.770 | 1.000 | 4519 | tags=30%, list=22%, signal=38% | |
1100 | RESPONSE TO PROGESTERONE | 7 | -0.55 | -1.16 | 0.313 | 0.770 | 1.000 | 5990 | tags=43%, list=29%, signal=60% | |
1101 | REGULATION OF WNT SIGNALING PATHWAY, PLANAR CELL POLARITY PATHWAY | 6 | -0.55 | -1.16 | 0.274 | 0.769 | 1.000 | 264 | tags=17%, list=1%, signal=17% | |
1102 | POSITIVE REGULATION OF ENDOTHELIAL CELL APOPTOTIC PROCESS | 7 | -0.56 | -1.16 | 0.317 | 0.769 | 1.000 | 108 | tags=29%, list=1%, signal=29% | |
1103 | POSITIVE REGULATION OF EPIDERMIS DEVELOPMENT | 15 | -0.40 | -1.16 | 0.288 | 0.769 | 1.000 | 6561 | tags=60%, list=32%, signal=88% | |
1104 | DOPAMINE BIOSYNTHETIC PROCESS | 5 | -0.60 | -1.16 | 0.285 | 0.768 | 1.000 | 160 | tags=20%, list=1%, signal=20% | |
1105 | NEGATIVE REGULATION OF STEM CELL PROLIFERATION | 10 | -0.46 | -1.16 | 0.309 | 0.768 | 1.000 | 2297 | tags=30%, list=11%, signal=34% | |
1106 | POSITIVE REGULATION OF CYTOSOLIC CALCIUM ION CONCENTRATION INVOLVED IN PHOSPHOLIPASE C-ACTIVATING G-PROTEIN COUPLED SIGNALING PATHWAY | 7 | -0.53 | -1.16 | 0.338 | 0.768 | 1.000 | 3494 | tags=43%, list=17%, signal=52% | |
1107 | REGULATION OF REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 34 | -0.36 | -1.16 | 0.240 | 0.768 | 1.000 | 6206 | tags=44%, list=30%, signal=63% | |
1108 | REGULATION OF ALPHA-AMINO-3-HYDROXY-5-METHYL-4-ISOXAZOLE PROPIONATE SELECTIVE GLUTAMATE RECEPTOR ACTIVITY | 18 | -0.43 | -1.16 | 0.316 | 0.769 | 1.000 | 6120 | tags=61%, list=30%, signal=87% | |
1109 | POSITIVE REGULATION OF CATECHOLAMINE SECRETION | 6 | -0.54 | -1.16 | 0.323 | 0.769 | 1.000 | 148 | tags=17%, list=1%, signal=17% | |
1110 | PHOSPHATIDYLINOSITOL 3-KINASE SIGNALING | 20 | -0.37 | -1.16 | 0.271 | 0.770 | 1.000 | 2125 | tags=20%, list=10%, signal=22% | |
1111 | RESPONSE TO GLUCOSE | 37 | -0.30 | -1.16 | 0.235 | 0.770 | 1.000 | 6939 | tags=46%, list=34%, signal=69% | |
1112 | DIVALENT INORGANIC CATION TRANSPORT | 151 | -0.27 | -1.16 | 0.229 | 0.770 | 1.000 | 5804 | tags=36%, list=28%, signal=49% | |
1113 | RESPONSE TO FORSKOLIN | 6 | -0.52 | -1.16 | 0.307 | 0.769 | 1.000 | 7840 | tags=83%, list=38%, signal=134% | |
1114 | CELLULAR RESPONSE TO FORSKOLIN | 6 | -0.52 | -1.16 | 0.307 | 0.769 | 1.000 | 7840 | tags=83%, list=38%, signal=134% | |
1115 | REGULATION OF NEURON DIFFERENTIATION | 381 | -0.24 | -1.16 | 0.199 | 0.769 | 1.000 | 6427 | tags=38%, list=31%, signal=54% | |
1116 | MOTOR NEURON AXON GUIDANCE | 27 | -0.36 | -1.16 | 0.265 | 0.769 | 1.000 | 4337 | tags=33%, list=21%, signal=42% | |
1117 | RESPONSE TO ACID CHEMICAL | 96 | -0.29 | -1.16 | 0.221 | 0.770 | 1.000 | 2933 | tags=24%, list=14%, signal=28% | |
1118 | SINGLE-ORGANISM CARBOHYDRATE CATABOLIC PROCESS | 59 | -0.35 | -1.16 | 0.291 | 0.770 | 1.000 | 4458 | tags=29%, list=22%, signal=37% | |
1119 | HEXOSE CATABOLIC PROCESS | 33 | -0.37 | -1.16 | 0.282 | 0.771 | 1.000 | 4458 | tags=30%, list=22%, signal=39% | |
1120 | REGULATION OF T CELL DIFFERENTIATION IN THYMUS | 13 | -0.41 | -1.16 | 0.277 | 0.771 | 1.000 | 2803 | tags=31%, list=14%, signal=36% | |
1121 | REGULATION OF THYMOCYTE AGGREGATION | 13 | -0.41 | -1.16 | 0.277 | 0.770 | 1.000 | 2803 | tags=31%, list=14%, signal=36% | |
1122 | REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 234 | -0.25 | -1.16 | 0.165 | 0.770 | 1.000 | 4566 | tags=27%, list=22%, signal=35% | |
1123 | REGULATION OF MICROTUBULE POLYMERIZATION | 16 | -0.37 | -1.16 | 0.267 | 0.772 | 1.000 | 212 | tags=13%, list=1%, signal=13% | |
1124 | BASE CONVERSION OR SUBSTITUTION EDITING | 7 | -0.51 | -1.16 | 0.297 | 0.771 | 1.000 | 1304 | tags=29%, list=6%, signal=30% | |
1125 | FOREBRAIN GENERATION OF NEURONS | 60 | -0.32 | -1.16 | 0.282 | 0.770 | 1.000 | 2062 | tags=18%, list=10%, signal=20% | |
1126 | REGULATION OF ORGAN GROWTH | 23 | -0.41 | -1.16 | 0.273 | 0.770 | 1.000 | 5264 | tags=48%, list=26%, signal=64% | |
1127 | CEREBELLAR GRANULAR LAYER DEVELOPMENT | 14 | -0.44 | -1.15 | 0.290 | 0.770 | 1.000 | 8303 | tags=71%, list=40%, signal=120% | |
1128 | REGULATION OF SMAD PROTEIN IMPORT INTO NUCLEUS | 13 | -0.44 | -1.15 | 0.284 | 0.770 | 1.000 | 4850 | tags=46%, list=24%, signal=60% | |
1129 | MORPHOGENESIS OF A BRANCHING STRUCTURE | 186 | -0.25 | -1.15 | 0.214 | 0.769 | 1.000 | 4914 | tags=30%, list=24%, signal=39% | |
1130 | TRIGLYCERIDE-RICH LIPOPROTEIN PARTICLE REMODELING | 8 | -0.53 | -1.15 | 0.305 | 0.769 | 1.000 | 5414 | tags=63%, list=26%, signal=85% | |
1131 | NEGATIVE REGULATION OF HETEROTYPIC CELL-CELL ADHESION | 7 | -0.50 | -1.15 | 0.311 | 0.769 | 1.000 | 1637 | tags=43%, list=8%, signal=47% | |
1132 | REGULATION OF CELL-CELL ADHESION INVOLVED IN GASTRULATION | 7 | -0.50 | -1.15 | 0.311 | 0.768 | 1.000 | 1637 | tags=43%, list=8%, signal=47% | |
1133 | NEGATIVE REGULATION OF MACROPHAGE DIFFERENTIATION | 5 | -0.63 | -1.15 | 0.346 | 0.768 | 1.000 | 3834 | tags=40%, list=19%, signal=49% | |
1134 | MACROPHAGE ACTIVATION | 11 | -0.46 | -1.15 | 0.287 | 0.767 | 1.000 | 6719 | tags=55%, list=33%, signal=81% | |
1135 | ASPARTATE FAMILY AMINO ACID CATABOLIC PROCESS | 14 | -0.44 | -1.15 | 0.328 | 0.767 | 1.000 | 2698 | tags=29%, list=13%, signal=33% | |
1136 | LIVER REGENERATION | 6 | -0.52 | -1.15 | 0.272 | 0.767 | 1.000 | 8180 | tags=67%, list=40%, signal=111% | |
1137 | REGULATION OF INTRACELLULAR STEROID HORMONE RECEPTOR SIGNALING PATHWAY | 44 | -0.33 | -1.15 | 0.264 | 0.767 | 1.000 | 4506 | tags=34%, list=22%, signal=44% | |
1138 | REGULATION OF LEUKOCYTE DIFFERENTIATION | 101 | -0.27 | -1.15 | 0.219 | 0.767 | 1.000 | 4042 | tags=27%, list=20%, signal=33% | |
1139 | OOGENESIS | 41 | -0.30 | -1.15 | 0.222 | 0.767 | 1.000 | 5050 | tags=39%, list=25%, signal=52% | |
1140 | ORGANOPHOSPHATE CATABOLIC PROCESS | 63 | -0.29 | -1.15 | 0.224 | 0.767 | 1.000 | 3070 | tags=24%, list=15%, signal=28% | |
1141 | NEGATIVE REGULATION OF RESPONSE TO WOUNDING | 76 | -0.31 | -1.15 | 0.250 | 0.767 | 1.000 | 7993 | tags=50%, list=39%, signal=81% | |
1142 | REGULATION OF ION TRANSPORT | 325 | -0.27 | -1.15 | 0.266 | 0.766 | 1.000 | 6270 | tags=38%, list=30%, signal=54% | |
1143 | BRANCHING INVOLVED IN URETERIC BUD MORPHOGENESIS | 46 | -0.32 | -1.15 | 0.274 | 0.767 | 1.000 | 4380 | tags=33%, list=21%, signal=41% | |
1144 | METAL ION TRANSPORT | 329 | -0.28 | -1.15 | 0.262 | 0.768 | 1.000 | 5686 | tags=36%, list=28%, signal=48% | |
1145 | REGULATION OF GLUCOSE METABOLIC PROCESS | 45 | -0.31 | -1.15 | 0.271 | 0.768 | 1.000 | 4049 | tags=24%, list=20%, signal=30% | |
1146 | MEMBRANE TUBULATION | 8 | -0.48 | -1.15 | 0.273 | 0.769 | 1.000 | 4366 | tags=50%, list=21%, signal=63% | |
1147 | REGULATION OF CELLULAR RESPONSE TO VASCULAR ENDOTHELIAL GROWTH FACTOR STIMULUS | 10 | -0.47 | -1.15 | 0.321 | 0.769 | 1.000 | 7022 | tags=60%, list=34%, signal=91% | |
1148 | ORGAN GROWTH | 68 | -0.29 | -1.15 | 0.232 | 0.769 | 1.000 | 6301 | tags=43%, list=31%, signal=61% | |
1149 | NEGATIVE REGULATION OF INTERLEUKIN-17 PRODUCTION | 8 | -0.52 | -1.15 | 0.320 | 0.768 | 1.000 | 5139 | tags=38%, list=25%, signal=50% | |
1150 | EXOCRINE PANCREAS DEVELOPMENT | 5 | -0.56 | -1.15 | 0.315 | 0.768 | 1.000 | 5743 | tags=60%, list=28%, signal=83% | |
1151 | ENTEROENDOCRINE CELL DIFFERENTIATION | 18 | -0.38 | -1.15 | 0.276 | 0.768 | 1.000 | 1523 | tags=17%, list=7%, signal=18% | |
1152 | HIS-PURKINJE SYSTEM DEVELOPMENT | 5 | -0.56 | -1.15 | 0.324 | 0.769 | 1.000 | 6973 | tags=60%, list=34%, signal=91% | |
1153 | CATION TRANSPORT | 442 | -0.26 | -1.15 | 0.234 | 0.768 | 1.000 | 6039 | tags=35%, list=29%, signal=48% | |
1154 | POSTSYNAPTIC MEMBRANE ORGANIZATION | 14 | -0.44 | -1.15 | 0.343 | 0.768 | 1.000 | 6147 | tags=43%, list=30%, signal=61% | |
1155 | POSITIVE REGULATION OF STRIATED MUSCLE CELL DIFFERENTIATION | 24 | -0.38 | -1.15 | 0.308 | 0.770 | 1.000 | 7577 | tags=58%, list=37%, signal=92% | |
1156 | HEART LOOPING | 56 | -0.29 | -1.15 | 0.226 | 0.770 | 1.000 | 3677 | tags=25%, list=18%, signal=30% | |
1157 | POSITIVE REGULATION OF MITOCHONDRIAL DEPOLARIZATION | 5 | -0.52 | -1.15 | 0.308 | 0.770 | 1.000 | 4820 | tags=40%, list=23%, signal=52% | |
1158 | REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 26 | -0.34 | -1.15 | 0.252 | 0.770 | 1.000 | 5854 | tags=38%, list=28%, signal=54% | |
1159 | REGULATION OF BLOOD CIRCULATION | 181 | -0.29 | -1.15 | 0.271 | 0.769 | 1.000 | 5804 | tags=39%, list=28%, signal=53% | |
1160 | PROSTATE GLAND GROWTH | 13 | -0.43 | -1.15 | 0.290 | 0.770 | 1.000 | 4914 | tags=54%, list=24%, signal=71% | |
1161 | INTRACELLULAR LIPID TRANSPORT | 16 | -0.41 | -1.15 | 0.277 | 0.769 | 1.000 | 1103 | tags=25%, list=5%, signal=26% | |
1162 | LEYDIG CELL DIFFERENTIATION | 9 | -0.45 | -1.15 | 0.275 | 0.770 | 1.000 | 4914 | tags=56%, list=24%, signal=73% | |
1163 | TOXIN METABOLIC PROCESS | 6 | -0.53 | -1.15 | 0.310 | 0.770 | 1.000 | 5370 | tags=50%, list=26%, signal=68% | |
1164 | POSITIVE REGULATION OF ACUTE INFLAMMATORY RESPONSE | 12 | -0.46 | -1.15 | 0.295 | 0.769 | 1.000 | 3878 | tags=33%, list=19%, signal=41% | |
1165 | POSITIVE REGULATION OF LIPID KINASE ACTIVITY | 22 | -0.38 | -1.15 | 0.293 | 0.769 | 1.000 | 5650 | tags=45%, list=27%, signal=63% | |
1166 | REGULATION OF TRANSMEMBRANE TRANSPORT | 261 | -0.27 | -1.15 | 0.283 | 0.769 | 1.000 | 6262 | tags=39%, list=30%, signal=55% | |
1167 | ANTERIOR/POSTERIOR AXON GUIDANCE | 5 | -0.59 | -1.15 | 0.344 | 0.769 | 1.000 | 5628 | tags=60%, list=27%, signal=83% | |
1168 | NEGATIVE REGULATION OF SEQUENCE-SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 104 | -0.28 | -1.15 | 0.240 | 0.769 | 1.000 | 4951 | tags=30%, list=24%, signal=39% | |
1169 | RESPONSE TO ETHANOL | 18 | -0.42 | -1.15 | 0.310 | 0.769 | 1.000 | 8645 | tags=61%, list=42%, signal=105% | |
1170 | REGULATION OF ENDOTHELIAL CELL MIGRATION | 91 | -0.29 | -1.14 | 0.278 | 0.769 | 1.000 | 7038 | tags=43%, list=34%, signal=65% | |
1171 | CELLULAR LIPID CATABOLIC PROCESS | 96 | -0.29 | -1.14 | 0.255 | 0.769 | 1.000 | 4924 | tags=34%, list=24%, signal=45% | |
1172 | EPIDERMAL CELL DIFFERENTIATION | 103 | -0.26 | -1.14 | 0.236 | 0.770 | 1.000 | 5372 | tags=34%, list=26%, signal=46% | |
1173 | REGULATION OF NOREPINEPHRINE SECRETION | 5 | -0.57 | -1.14 | 0.337 | 0.771 | 1.000 | 4264 | tags=40%, list=21%, signal=50% | |
1174 | MALE SEX DIFFERENTIATION | 116 | -0.26 | -1.14 | 0.224 | 0.771 | 1.000 | 2221 | tags=17%, list=11%, signal=19% | |
1175 | REGULATION OF PLASMA LIPOPROTEIN PARTICLE LEVELS | 35 | -0.35 | -1.14 | 0.278 | 0.771 | 1.000 | 3581 | tags=31%, list=17%, signal=38% | |
1176 | OLIGOSACCHARIDE METABOLIC PROCESS | 27 | -0.32 | -1.14 | 0.266 | 0.772 | 1.000 | 1561 | tags=22%, list=8%, signal=24% | |
1177 | CARBOHYDRATE CATABOLIC PROCESS | 61 | -0.34 | -1.14 | 0.314 | 0.773 | 1.000 | 4458 | tags=30%, list=22%, signal=38% | |
1178 | PHOSPHOLIPID TRANSPORT | 32 | -0.35 | -1.14 | 0.251 | 0.773 | 1.000 | 4010 | tags=34%, list=19%, signal=43% | |
1179 | MALE GONAD DEVELOPMENT | 93 | -0.26 | -1.14 | 0.214 | 0.774 | 1.000 | 837 | tags=13%, list=4%, signal=13% | |
1180 | DEVELOPMENT OF PRIMARY MALE SEXUAL CHARACTERISTICS | 93 | -0.26 | -1.14 | 0.214 | 0.774 | 1.000 | 837 | tags=13%, list=4%, signal=13% | |
1181 | NEGATIVE REGULATION OF TISSUE REMODELING | 6 | -0.55 | -1.14 | 0.337 | 0.773 | 1.000 | 790 | tags=33%, list=4%, signal=35% | |
1182 | POSITIVE REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 11 | -0.46 | -1.14 | 0.291 | 0.776 | 1.000 | 108 | tags=18%, list=1%, signal=18% | |
1183 | KIDNEY DEVELOPMENT | 203 | -0.24 | -1.14 | 0.207 | 0.777 | 1.000 | 4418 | tags=29%, list=21%, signal=36% | |
1184 | NEGATIVE REGULATION OF T CELL CYTOKINE PRODUCTION | 5 | -0.55 | -1.14 | 0.331 | 0.776 | 1.000 | 3278 | tags=40%, list=16%, signal=48% | |
1185 | WATER TRANSPORT | 36 | -0.32 | -1.14 | 0.269 | 0.776 | 1.000 | 7840 | tags=53%, list=38%, signal=85% | |
1186 | LEARNING | 35 | -0.35 | -1.14 | 0.294 | 0.777 | 1.000 | 9352 | tags=63%, list=45%, signal=115% | |
1187 | NEUTRAL LIPID METABOLIC PROCESS | 79 | -0.29 | -1.14 | 0.236 | 0.776 | 1.000 | 4751 | tags=34%, list=23%, signal=44% | |
1188 | ACYLGLYCEROL METABOLIC PROCESS | 79 | -0.29 | -1.14 | 0.236 | 0.776 | 1.000 | 4751 | tags=34%, list=23%, signal=44% | |
1189 | POSITIVE REGULATION OF MUSCLE TISSUE DEVELOPMENT | 26 | -0.35 | -1.14 | 0.301 | 0.775 | 1.000 | 7577 | tags=50%, list=37%, signal=79% | |
1190 | ENSHEATHMENT OF NEURONS | 75 | -0.27 | -1.14 | 0.204 | 0.775 | 1.000 | 3524 | tags=25%, list=17%, signal=30% | |
1191 | AXON ENSHEATHMENT | 75 | -0.27 | -1.14 | 0.204 | 0.774 | 1.000 | 3524 | tags=25%, list=17%, signal=30% | |
1192 | POSITIVE REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 42 | -0.33 | -1.14 | 0.295 | 0.774 | 1.000 | 5814 | tags=38%, list=28%, signal=53% | |
1193 | BLOOD COAGULATION, FIBRIN CLOT FORMATION | 25 | -0.40 | -1.14 | 0.306 | 0.775 | 1.000 | 5152 | tags=44%, list=25%, signal=59% | |
1194 | CARDIAC CONDUCTION | 114 | -0.30 | -1.14 | 0.303 | 0.775 | 1.000 | 5804 | tags=41%, list=28%, signal=57% | |
1195 | REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 20 | -0.37 | -1.14 | 0.304 | 0.775 | 1.000 | 4336 | tags=40%, list=21%, signal=51% | |
1196 | MULTICELLULAR ORGANISMAL RESPONSE TO STRESS | 12 | -0.45 | -1.14 | 0.319 | 0.776 | 1.000 | 2544 | tags=33%, list=12%, signal=38% | |
1197 | AMMONIUM TRANSMEMBRANE TRANSPORT | 24 | -0.36 | -1.14 | 0.267 | 0.777 | 1.000 | 3625 | tags=29%, list=18%, signal=35% | |
1198 | NEGATIVE REGULATION OF PROTEIN LOCALIZATION TO CELL SURFACE | 6 | -0.51 | -1.14 | 0.320 | 0.777 | 1.000 | 675 | tags=17%, list=3%, signal=17% | |
1199 | TRIGEMINAL GANGLION DEVELOPMENT | 5 | -0.59 | -1.14 | 0.344 | 0.777 | 1.000 | 6442 | tags=60%, list=31%, signal=87% | |
1200 | ANGIOTENSIN MATURATION | 12 | -0.45 | -1.14 | 0.297 | 0.776 | 1.000 | 3574 | tags=42%, list=17%, signal=50% | |
1201 | INORGANIC ION TRANSMEMBRANE TRANSPORT | 345 | -0.27 | -1.13 | 0.267 | 0.778 | 1.000 | 6111 | tags=36%, list=30%, signal=50% | |
1202 | REGULATION OF MYELOID LEUKOCYTE DIFFERENTIATION | 49 | -0.30 | -1.13 | 0.255 | 0.777 | 1.000 | 3937 | tags=27%, list=19%, signal=33% | |
1203 | DRUG CATABOLIC PROCESS | 11 | -0.43 | -1.13 | 0.315 | 0.780 | 1.000 | 6407 | tags=64%, list=31%, signal=92% | |
1204 | DNA ALKYLATION | 35 | -0.32 | -1.13 | 0.265 | 0.779 | 1.000 | 6007 | tags=31%, list=29%, signal=44% | |
1205 | DNA METHYLATION | 35 | -0.32 | -1.13 | 0.265 | 0.779 | 1.000 | 6007 | tags=31%, list=29%, signal=44% | |
1206 | LUNG EPITHELIUM DEVELOPMENT | 40 | -0.32 | -1.13 | 0.301 | 0.778 | 1.000 | 4761 | tags=40%, list=23%, signal=52% | |
1207 | INOSITOL PHOSPHATE METABOLIC PROCESS | 40 | -0.31 | -1.13 | 0.272 | 0.780 | 1.000 | 1442 | tags=18%, list=7%, signal=19% | |
1208 | 4-HYDROXYPROLINE METABOLIC PROCESS | 7 | -0.46 | -1.13 | 0.304 | 0.779 | 1.000 | 4535 | tags=43%, list=22%, signal=55% | |
1209 | ICOSANOID METABOLIC PROCESS | 54 | -0.32 | -1.13 | 0.283 | 0.780 | 1.000 | 3878 | tags=30%, list=19%, signal=36% | |
1210 | FATTY ACID DERIVATIVE METABOLIC PROCESS | 54 | -0.32 | -1.13 | 0.283 | 0.780 | 1.000 | 3878 | tags=30%, list=19%, signal=36% | |
1211 | APPENDAGE DEVELOPMENT | 156 | -0.26 | -1.13 | 0.251 | 0.779 | 1.000 | 6528 | tags=44%, list=32%, signal=63% | |
1212 | LIMB DEVELOPMENT | 156 | -0.26 | -1.13 | 0.251 | 0.779 | 1.000 | 6528 | tags=44%, list=32%, signal=63% | |
1213 | RESPONSE TO BMP | 52 | -0.31 | -1.13 | 0.264 | 0.779 | 1.000 | 4850 | tags=37%, list=24%, signal=48% | |
1214 | CELLULAR RESPONSE TO BMP STIMULUS | 52 | -0.31 | -1.13 | 0.264 | 0.779 | 1.000 | 4850 | tags=37%, list=24%, signal=48% | |
1215 | POTASSIUM ION TRANSPORT | 97 | -0.34 | -1.13 | 0.324 | 0.781 | 1.000 | 5686 | tags=42%, list=28%, signal=58% | |
1216 | PHENOL-CONTAINING COMPOUND METABOLIC PROCESS | 31 | -0.37 | -1.13 | 0.331 | 0.780 | 1.000 | 5066 | tags=32%, list=25%, signal=43% | |
1217 | PRESYNAPTIC PROCESS INVOLVED IN SYNAPTIC TRANSMISSION | 15 | -0.42 | -1.13 | 0.310 | 0.781 | 1.000 | 3091 | tags=33%, list=15%, signal=39% | |
1218 | ESTABLISHMENT OF BLOOD-NERVE BARRIER | 5 | -0.56 | -1.13 | 0.353 | 0.780 | 1.000 | 7516 | tags=80%, list=36%, signal=126% | |
1219 | WNT SIGNALING PATHWAY, PLANAR CELL POLARITY PATHWAY | 17 | -0.38 | -1.13 | 0.294 | 0.780 | 1.000 | 3428 | tags=35%, list=17%, signal=42% | |
1220 | RNA METHYLATION | 11 | -0.51 | -1.13 | 0.359 | 0.780 | 1.000 | 3829 | tags=27%, list=19%, signal=33% | |
1221 | MONOSACCHARIDE CATABOLIC PROCESS | 38 | -0.35 | -1.13 | 0.301 | 0.779 | 1.000 | 4458 | tags=29%, list=22%, signal=37% | |
1222 | POSITIVE REGULATION OF OLIGODENDROCYTE DIFFERENTIATION | 8 | -0.45 | -1.13 | 0.309 | 0.780 | 1.000 | 6277 | tags=63%, list=30%, signal=90% | |
1223 | CELLULAR POTASSIUM ION TRANSPORT | 88 | -0.34 | -1.13 | 0.327 | 0.780 | 1.000 | 5686 | tags=44%, list=28%, signal=61% | |
1224 | POTASSIUM ION TRANSMEMBRANE TRANSPORT | 88 | -0.34 | -1.13 | 0.327 | 0.780 | 1.000 | 5686 | tags=44%, list=28%, signal=61% | |
1225 | NEGATIVE REGULATION OF HEMOPOIESIS | 65 | -0.29 | -1.13 | 0.263 | 0.779 | 1.000 | 4047 | tags=28%, list=20%, signal=34% | |
1226 | SEMAPHORIN-PLEXIN SIGNALING PATHWAY | 18 | -0.41 | -1.13 | 0.352 | 0.779 | 1.000 | 5173 | tags=44%, list=25%, signal=59% | |
1227 | NEGATIVE REGULATION OF GLIAL CELL DIFFERENTIATION | 20 | -0.40 | -1.13 | 0.300 | 0.781 | 1.000 | 3799 | tags=25%, list=18%, signal=31% | |
1228 | POSITIVE REGULATION OF ENDOTHELIAL CELL DIFFERENTIATION | 6 | -0.53 | -1.13 | 0.335 | 0.782 | 1.000 | 298 | tags=17%, list=1%, signal=17% | |
1229 | POSITIVE REGULATION OF AXON EXTENSION | 26 | -0.34 | -1.13 | 0.312 | 0.782 | 1.000 | 2285 | tags=27%, list=11%, signal=30% | |
1230 | CEREBELLAR GRANULAR LAYER MORPHOGENESIS | 11 | -0.45 | -1.13 | 0.335 | 0.781 | 1.000 | 6120 | tags=55%, list=30%, signal=78% | |
1231 | LACRIMAL GLAND DEVELOPMENT | 8 | -0.51 | -1.13 | 0.355 | 0.781 | 1.000 | 5503 | tags=50%, list=27%, signal=68% | |
1232 | REGULATION OF VASODILATION | 9 | -0.45 | -1.13 | 0.331 | 0.783 | 1.000 | 2134 | tags=33%, list=10%, signal=37% | |
1233 | POSITIVE REGULATION OF EPIDERMAL GROWTH FACTOR-ACTIVATED RECEPTOR ACTIVITY | 8 | -0.46 | -1.13 | 0.298 | 0.783 | 1.000 | 4264 | tags=50%, list=21%, signal=63% | |
1234 | SALIVARY GLAND DEVELOPMENT | 34 | -0.34 | -1.13 | 0.322 | 0.783 | 1.000 | 4336 | tags=35%, list=21%, signal=45% | |
1235 | NEGATIVE REGULATION OF RAS PROTEIN SIGNAL TRANSDUCTION | 13 | -0.40 | -1.13 | 0.321 | 0.782 | 1.000 | 6680 | tags=54%, list=32%, signal=80% | |
1236 | PARANODAL JUNCTION ASSEMBLY | 6 | -0.51 | -1.12 | 0.325 | 0.783 | 1.000 | 4576 | tags=50%, list=22%, signal=64% | |
1237 | EPITHELIAL TO MESENCHYMAL TRANSITION | 53 | -0.29 | -1.12 | 0.255 | 0.783 | 1.000 | 2361 | tags=17%, list=11%, signal=19% | |
1238 | RESPONSE TO PLATELET-DERIVED GROWTH FACTOR | 8 | -0.51 | -1.12 | 0.336 | 0.782 | 1.000 | 5493 | tags=63%, list=27%, signal=85% | |
1239 | MUCOSAL-ASSOCIATED LYMPHOID TISSUE DEVELOPMENT | 12 | -0.40 | -1.12 | 0.297 | 0.782 | 1.000 | 7834 | tags=50%, list=38%, signal=81% | |
1240 | PEYER'S PATCH DEVELOPMENT | 12 | -0.40 | -1.12 | 0.297 | 0.781 | 1.000 | 7834 | tags=50%, list=38%, signal=81% | |
1241 | VASCULAR ENDOTHELIAL GROWTH FACTOR SIGNALING PATHWAY | 12 | -0.45 | -1.12 | 0.331 | 0.781 | 1.000 | 5814 | tags=50%, list=28%, signal=70% | |
1242 | CIRCULATORY SYSTEM PROCESS | 181 | -0.29 | -1.12 | 0.276 | 0.781 | 1.000 | 3896 | tags=28%, list=19%, signal=34% | |
1243 | MIDBRAIN DEVELOPMENT | 81 | -0.27 | -1.12 | 0.250 | 0.781 | 1.000 | 2803 | tags=17%, list=14%, signal=20% | |
1244 | SEMICIRCULAR CANAL MORPHOGENESIS | 7 | -0.49 | -1.12 | 0.322 | 0.780 | 1.000 | 4380 | tags=43%, list=21%, signal=54% | |
1245 | SENSORY ORGAN MORPHOGENESIS | 255 | -0.25 | -1.12 | 0.300 | 0.780 | 1.000 | 7002 | tags=44%, list=34%, signal=65% | |
1246 | MYOBLAST FUSION | 19 | -0.43 | -1.12 | 0.350 | 0.782 | 1.000 | 5715 | tags=53%, list=28%, signal=73% | |
1247 | REGULATION OF SINGLE STRANDED VIRAL RNA REPLICATION VIA DOUBLE STRANDED DNA INTERMEDIATE | 5 | -0.61 | -1.12 | 0.371 | 0.781 | 1.000 | 333 | tags=20%, list=2%, signal=20% | |
1248 | AXONEME ASSEMBLY | 29 | -0.34 | -1.12 | 0.271 | 0.781 | 1.000 | 5901 | tags=38%, list=29%, signal=53% | |
1249 | VESTIBULOCOCHLEAR NERVE DEVELOPMENT | 7 | -0.50 | -1.12 | 0.345 | 0.780 | 1.000 | 6755 | tags=57%, list=33%, signal=85% | |
1250 | REGULATION OF HEART GROWTH | 18 | -0.40 | -1.12 | 0.317 | 0.780 | 1.000 | 6094 | tags=50%, list=30%, signal=71% | |
1251 | POSITIVE REGULATION OF DNA RECOMBINATION | 7 | -0.49 | -1.12 | 0.317 | 0.780 | 1.000 | 5359 | tags=57%, list=26%, signal=77% | |
1252 | NEGATIVE REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 17 | -0.39 | -1.12 | 0.310 | 0.780 | 1.000 | 792 | tags=18%, list=4%, signal=18% | |
1253 | CARDIOCYTE DIFFERENTIATION | 85 | -0.27 | -1.12 | 0.272 | 0.780 | 1.000 | 5582 | tags=39%, list=27%, signal=53% | |
1254 | CAMERA-TYPE EYE PHOTORECEPTOR CELL DIFFERENTIATION | 20 | -0.36 | -1.12 | 0.287 | 0.780 | 1.000 | 5372 | tags=45%, list=26%, signal=61% | |
1255 | REGULATION OF OXIDATIVE STRESS-INDUCED NEURON DEATH | 10 | -0.38 | -1.12 | 0.304 | 0.780 | 1.000 | 4323 | tags=40%, list=21%, signal=51% | |
1256 | PHOSPHATIDYLSERINE ACYL-CHAIN REMODELING | 14 | -0.41 | -1.12 | 0.324 | 0.780 | 1.000 | 5479 | tags=43%, list=27%, signal=58% | |
1257 | DORSAL SPINAL CORD DEVELOPMENT | 15 | -0.43 | -1.12 | 0.356 | 0.780 | 1.000 | 6727 | tags=40%, list=33%, signal=59% | |
1258 | POSITIVE REGULATION OF T CELL DIFFERENTIATION IN THYMUS | 5 | -0.57 | -1.12 | 0.355 | 0.779 | 1.000 | 2803 | tags=60%, list=14%, signal=69% | |
1259 | POSITIVE REGULATION OF THYMOCYTE AGGREGATION | 5 | -0.57 | -1.12 | 0.355 | 0.779 | 1.000 | 2803 | tags=60%, list=14%, signal=69% | |
1260 | PURINE-CONTAINING COMPOUND CATABOLIC PROCESS | 35 | -0.33 | -1.12 | 0.297 | 0.780 | 1.000 | 6511 | tags=43%, list=32%, signal=63% | |
1261 | RESPONSE TO LIGHT STIMULUS | 218 | -0.24 | -1.12 | 0.233 | 0.780 | 1.000 | 5552 | tags=30%, list=27%, signal=41% | |
1262 | NEGATIVE REGULATION OF G2/M TRANSITION OF MITOTIC CELL CYCLE | 10 | -0.46 | -1.12 | 0.313 | 0.780 | 1.000 | 2678 | tags=30%, list=13%, signal=34% | |
1263 | REGULATION OF URINE VOLUME | 8 | -0.51 | -1.12 | 0.381 | 0.780 | 1.000 | 6315 | tags=50%, list=31%, signal=72% | |
1264 | QUATERNARY AMMONIUM GROUP TRANSPORT | 14 | -0.42 | -1.12 | 0.307 | 0.780 | 1.000 | 1695 | tags=29%, list=8%, signal=31% | |
1265 | NEGATIVE REGULATION OF LIPID METABOLIC PROCESS | 45 | -0.32 | -1.12 | 0.316 | 0.779 | 1.000 | 7812 | tags=56%, list=38%, signal=89% | |
1266 | BRANCHING INVOLVED IN LABYRINTHINE LAYER MORPHOGENESIS | 13 | -0.44 | -1.12 | 0.313 | 0.781 | 1.000 | 2211 | tags=23%, list=11%, signal=26% | |
1267 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER INVOLVED IN MYOCARDIAL PRECURSOR CELL DIFFERENTIATION | 6 | -0.50 | -1.12 | 0.345 | 0.780 | 1.000 | 5287 | tags=50%, list=26%, signal=67% | |
1268 | MELANOSOME TRANSPORT | 11 | -0.37 | -1.12 | 0.311 | 0.781 | 1.000 | 7002 | tags=55%, list=34%, signal=83% | |
1269 | PIGMENT GRANULE TRANSPORT | 11 | -0.37 | -1.12 | 0.311 | 0.780 | 1.000 | 7002 | tags=55%, list=34%, signal=83% | |
1270 | EPOXYGENASE P450 PATHWAY | 11 | -0.44 | -1.12 | 0.324 | 0.780 | 1.000 | 5590 | tags=55%, list=27%, signal=75% | |
1271 | POSITIVE REGULATION OF SYNAPTIC TRANSMISSION, GLUTAMATERGIC | 9 | -0.43 | -1.12 | 0.318 | 0.780 | 1.000 | 6120 | tags=56%, list=30%, signal=79% | |
1272 | REGULATION OF ACTIN FILAMENT-BASED PROCESS | 176 | -0.25 | -1.12 | 0.237 | 0.780 | 1.000 | 5317 | tags=33%, list=26%, signal=44% | |
1273 | FACE MORPHOGENESIS | 31 | -0.33 | -1.12 | 0.276 | 0.780 | 1.000 | 3799 | tags=26%, list=18%, signal=32% | |
1274 | BONE GROWTH | 21 | -0.39 | -1.12 | 0.323 | 0.779 | 1.000 | 6071 | tags=52%, list=29%, signal=74% | |
1275 | TRIPARTITE REGIONAL SUBDIVISION | 11 | -0.45 | -1.12 | 0.371 | 0.779 | 1.000 | 6710 | tags=73%, list=33%, signal=108% | |
1276 | ANTERIOR/POSTERIOR AXIS SPECIFICATION, EMBRYO | 11 | -0.45 | -1.12 | 0.371 | 0.778 | 1.000 | 6710 | tags=73%, list=33%, signal=108% | |
1277 | REGULATION OF HYDROGEN PEROXIDE-MEDIATED PROGRAMMED CELL DEATH | 6 | -0.52 | -1.12 | 0.368 | 0.777 | 1.000 | 5989 | tags=67%, list=29%, signal=94% | |
1278 | STEM CELL PROLIFERATION | 55 | -0.27 | -1.12 | 0.261 | 0.777 | 1.000 | 5688 | tags=40%, list=28%, signal=55% | |
1279 | CHONDROCYTE DEVELOPMENT INVOLVED IN ENDOCHONDRAL BONE MORPHOGENESIS | 5 | -0.57 | -1.12 | 0.366 | 0.777 | 1.000 | 3732 | tags=40%, list=18%, signal=49% | |
1280 | ESTABLISHMENT OF MELANOSOME LOCALIZATION | 12 | -0.37 | -1.12 | 0.314 | 0.777 | 1.000 | 7002 | tags=50%, list=34%, signal=76% | |
1281 | ESTABLISHMENT OF PIGMENT GRANULE LOCALIZATION | 12 | -0.37 | -1.12 | 0.314 | 0.776 | 1.000 | 7002 | tags=50%, list=34%, signal=76% | |
1282 | 2'-DEOXYRIBONUCLEOTIDE METABOLIC PROCESS | 19 | -0.43 | -1.12 | 0.338 | 0.776 | 1.000 | 2575 | tags=32%, list=12%, signal=36% | |
1283 | DEOXYRIBOSE PHOSPHATE METABOLIC PROCESS | 19 | -0.43 | -1.12 | 0.338 | 0.776 | 1.000 | 2575 | tags=32%, list=12%, signal=36% | |
1284 | CELLULAR RESPONSE TO REACTIVE OXYGEN SPECIES | 53 | -0.30 | -1.12 | 0.296 | 0.777 | 1.000 | 3090 | tags=23%, list=15%, signal=27% | |
1285 | PHOSPHOLIPASE C-ACTIVATING G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 34 | -0.37 | -1.12 | 0.327 | 0.776 | 1.000 | 3717 | tags=29%, list=18%, signal=36% | |
1286 | REGULATION OF PROTEIN TYROSINE KINASE ACTIVITY | 47 | -0.29 | -1.12 | 0.259 | 0.776 | 1.000 | 4264 | tags=30%, list=21%, signal=37% | |
1287 | AMMONIUM TRANSPORT | 32 | -0.33 | -1.12 | 0.296 | 0.776 | 1.000 | 3625 | tags=25%, list=18%, signal=30% | |
1288 | POSITIVE REGULATION OF EPITHELIAL CELL MIGRATION | 79 | -0.28 | -1.12 | 0.255 | 0.775 | 1.000 | 5157 | tags=33%, list=25%, signal=44% | |
1289 | NEURON MIGRATION | 107 | -0.26 | -1.12 | 0.266 | 0.776 | 1.000 | 3658 | tags=23%, list=18%, signal=28% | |
1290 | MITOTIC G2 DNA DAMAGE CHECKPOINT | 7 | -0.52 | -1.12 | 0.342 | 0.775 | 1.000 | 435 | tags=29%, list=2%, signal=29% | |
1291 | REGULATION OF ION HOMEOSTASIS | 111 | -0.26 | -1.12 | 0.298 | 0.776 | 1.000 | 5705 | tags=33%, list=28%, signal=46% | |
1292 | DEFINITIVE HEMOPOIESIS | 20 | -0.37 | -1.11 | 0.311 | 0.777 | 1.000 | 3082 | tags=35%, list=15%, signal=41% | |
1293 | POSITIVE REGULATION OF INSULIN SECRETION | 21 | -0.35 | -1.11 | 0.313 | 0.778 | 1.000 | 1171 | tags=14%, list=6%, signal=15% | |
1294 | HIGH-DENSITY LIPOPROTEIN PARTICLE REMODELING | 14 | -0.41 | -1.11 | 0.306 | 0.778 | 1.000 | 3155 | tags=29%, list=15%, signal=34% | |
1295 | PLASMA LIPOPROTEIN PARTICLE CLEARANCE | 18 | -0.40 | -1.11 | 0.318 | 0.779 | 1.000 | 3581 | tags=39%, list=17%, signal=47% | |
1296 | INNER EAR DEVELOPMENT | 171 | -0.26 | -1.11 | 0.290 | 0.780 | 1.000 | 6107 | tags=36%, list=30%, signal=50% | |
1297 | COLLAGEN FIBRIL ORGANIZATION | 15 | -0.42 | -1.11 | 0.351 | 0.780 | 1.000 | 3935 | tags=33%, list=19%, signal=41% | |
1298 | FOREBRAIN NEURON DIFFERENTIATION | 49 | -0.33 | -1.11 | 0.353 | 0.784 | 1.000 | 2062 | tags=18%, list=10%, signal=20% | |
1299 | HIPPOCAMPUS DEVELOPMENT | 51 | -0.28 | -1.11 | 0.280 | 0.783 | 1.000 | 5312 | tags=29%, list=26%, signal=40% | |
1300 | CONVERGENT EXTENSION INVOLVED IN ORGANOGENESIS | 6 | -0.55 | -1.11 | 0.384 | 0.785 | 1.000 | 7698 | tags=83%, list=37%, signal=133% | |
1301 | NEGATIVE REGULATION OF INTERLEUKIN-2 PRODUCTION | 9 | -0.48 | -1.11 | 0.348 | 0.784 | 1.000 | 4372 | tags=44%, list=21%, signal=56% | |
1302 | BLOOD CIRCULATION | 180 | -0.28 | -1.11 | 0.292 | 0.786 | 1.000 | 3896 | tags=28%, list=19%, signal=34% | |
1303 | LIPOXYGENASE PATHWAY | 12 | -0.43 | -1.11 | 0.303 | 0.788 | 1.000 | 683 | tags=17%, list=3%, signal=17% | |
1304 | MULTICELLULAR ORGANISMAL AGING | 26 | -0.32 | -1.11 | 0.303 | 0.787 | 1.000 | 3392 | tags=27%, list=16%, signal=32% | |
1305 | POSITIVE REGULATION OF DNA REPLICATION | 65 | -0.31 | -1.11 | 0.320 | 0.787 | 1.000 | 4049 | tags=29%, list=20%, signal=36% | |
1306 | NEGATIVE REGULATION OF FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 6 | -0.50 | -1.11 | 0.340 | 0.789 | 1.000 | 8180 | tags=67%, list=40%, signal=111% | |
1307 | NEGATIVE REGULATION OF PLATELET ACTIVATION | 12 | -0.43 | -1.11 | 0.310 | 0.789 | 1.000 | 8902 | tags=75%, list=43%, signal=132% | |
1308 | AXIAL MESODERM MORPHOGENESIS | 5 | -0.55 | -1.11 | 0.358 | 0.789 | 1.000 | 6397 | tags=60%, list=31%, signal=87% | |
1309 | PROTEOGLYCAN BIOSYNTHETIC PROCESS | 27 | -0.36 | -1.11 | 0.324 | 0.791 | 1.000 | 3927 | tags=37%, list=19%, signal=46% | |
1310 | REGULATION OF GRANULOCYTE DIFFERENTIATION | 10 | -0.41 | -1.11 | 0.344 | 0.791 | 1.000 | 3937 | tags=40%, list=19%, signal=49% | |
1311 | SYNCYTIUM FORMATION BY PLASMA MEMBRANE FUSION | 22 | -0.40 | -1.11 | 0.359 | 0.791 | 1.000 | 5715 | tags=45%, list=28%, signal=63% | |
1312 | REGULATION OF SYNAPSE MATURATION | 9 | -0.46 | -1.10 | 0.371 | 0.793 | 1.000 | 8089 | tags=67%, list=39%, signal=110% | |
1313 | POSITIVE REGULATION OF FOCAL ADHESION ASSEMBLY | 13 | -0.38 | -1.10 | 0.337 | 0.792 | 1.000 | 8841 | tags=62%, list=43%, signal=108% | |
1314 | REGULATION OF CELLULAR CARBOHYDRATE METABOLIC PROCESS | 74 | -0.27 | -1.10 | 0.291 | 0.793 | 1.000 | 4049 | tags=24%, list=20%, signal=30% | |
1315 | REGULATION OF ION TRANSMEMBRANE TRANSPORT | 251 | -0.27 | -1.10 | 0.331 | 0.795 | 1.000 | 6262 | tags=39%, list=30%, signal=55% | |
1316 | REGULATION OF NEURON PROJECTION DEVELOPMENT | 264 | -0.23 | -1.10 | 0.256 | 0.797 | 1.000 | 6427 | tags=38%, list=31%, signal=54% | |
1317 | OXIDATIVE DEMETHYLATION | 12 | -0.39 | -1.10 | 0.324 | 0.796 | 1.000 | 5651 | tags=50%, list=27%, signal=69% | |
1318 | POSITIVE REGULATION OF RECEPTOR ACTIVITY | 37 | -0.31 | -1.10 | 0.333 | 0.798 | 1.000 | 5312 | tags=38%, list=26%, signal=51% | |
1319 | REGULATION OF N-METHYL-D-ASPARTATE SELECTIVE GLUTAMATE RECEPTOR ACTIVITY | 11 | -0.45 | -1.10 | 0.356 | 0.797 | 1.000 | 6238 | tags=55%, list=30%, signal=78% | |
1320 | REGULATION OF EPITHELIAL CELL MIGRATION | 129 | -0.26 | -1.10 | 0.252 | 0.797 | 1.000 | 4997 | tags=29%, list=24%, signal=38% | |
1321 | REGULATION OF BROWN FAT CELL DIFFERENTIATION | 7 | -0.52 | -1.10 | 0.356 | 0.796 | 1.000 | 6950 | tags=71%, list=34%, signal=108% | |
1322 | POSITIVE REGULATION OF REGULATED SECRETORY PATHWAY | 25 | -0.34 | -1.10 | 0.331 | 0.796 | 1.000 | 4255 | tags=36%, list=21%, signal=45% | |
1323 | POSITIVE REGULATION OF DEVELOPMENTAL GROWTH | 76 | -0.30 | -1.10 | 0.337 | 0.796 | 1.000 | 6183 | tags=42%, list=30%, signal=60% | |
1324 | GLYCOLYTIC PROCESS | 26 | -0.37 | -1.10 | 0.340 | 0.796 | 1.000 | 4394 | tags=27%, list=21%, signal=34% | |
1325 | ATP GENERATION FROM ADP | 26 | -0.37 | -1.10 | 0.340 | 0.795 | 1.000 | 4394 | tags=27%, list=21%, signal=34% | |
1326 | PURINERGIC RECEPTOR SIGNALING PATHWAY | 7 | -0.53 | -1.10 | 0.357 | 0.795 | 1.000 | 107 | tags=14%, list=1%, signal=14% | |
1327 | CORNEA DEVELOPMENT IN CAMERA-TYPE EYE | 11 | -0.46 | -1.10 | 0.376 | 0.795 | 1.000 | 5437 | tags=45%, list=26%, signal=62% | |
1328 | KERATAN SULFATE METABOLIC PROCESS | 31 | -0.32 | -1.10 | 0.322 | 0.794 | 1.000 | 3463 | tags=29%, list=17%, signal=35% | |
1329 | NEGATIVE REGULATION OF PROTEIN POLYMERIZATION | 18 | -0.37 | -1.10 | 0.321 | 0.796 | 1.000 | 769 | tags=17%, list=4%, signal=17% | |
1330 | ALCOHOL METABOLIC PROCESS | 206 | -0.24 | -1.10 | 0.268 | 0.796 | 1.000 | 4924 | tags=27%, list=24%, signal=35% | |
1331 | KIDNEY EPITHELIUM DEVELOPMENT | 102 | -0.27 | -1.10 | 0.289 | 0.795 | 1.000 | 4745 | tags=32%, list=23%, signal=42% | |
1332 | PLATELET MORPHOGENESIS | 19 | -0.38 | -1.10 | 0.356 | 0.795 | 1.000 | 1260 | tags=21%, list=6%, signal=22% | |
1333 | REGULATION OF NEUROTRANSMITTER LEVELS | 98 | -0.28 | -1.10 | 0.316 | 0.796 | 1.000 | 3220 | tags=26%, list=16%, signal=30% | |
1334 | NUCLEOSIDE DIPHOSPHATE PHOSPHORYLATION | 31 | -0.36 | -1.10 | 0.340 | 0.796 | 1.000 | 4394 | tags=26%, list=21%, signal=33% | |
1335 | AORTIC VALVE DEVELOPMENT | 6 | -0.53 | -1.10 | 0.372 | 0.796 | 1.000 | 6504 | tags=50%, list=32%, signal=73% | |
1336 | AORTIC VALVE MORPHOGENESIS | 6 | -0.53 | -1.10 | 0.372 | 0.795 | 1.000 | 6504 | tags=50%, list=32%, signal=73% | |
1337 | NEGATIVE REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 14 | -0.38 | -1.10 | 0.329 | 0.795 | 1.000 | 6680 | tags=50%, list=32%, signal=74% | |
1338 | COBALAMIN METABOLIC PROCESS | 19 | -0.35 | -1.10 | 0.324 | 0.797 | 1.000 | 5256 | tags=37%, list=26%, signal=49% | |
1339 | EMBRYONIC FORELIMB MORPHOGENESIS | 32 | -0.32 | -1.10 | 0.359 | 0.798 | 1.000 | 6504 | tags=50%, list=32%, signal=73% | |
1340 | MULTICELLULAR ORGANISMAL CATABOLIC PROCESS | 62 | -0.32 | -1.10 | 0.367 | 0.798 | 1.000 | 5912 | tags=47%, list=29%, signal=65% | |
1341 | CARBOXYLIC ACID TRANSPORT | 162 | -0.26 | -1.10 | 0.299 | 0.797 | 1.000 | 3494 | tags=23%, list=17%, signal=28% | |
1342 | SODIUM-INDEPENDENT ORGANIC ANION TRANSPORT | 13 | -0.39 | -1.10 | 0.327 | 0.797 | 1.000 | 2705 | tags=23%, list=13%, signal=27% | |
1343 | TRNA THREONYLCARBAMOYLADENOSINE METABOLIC PROCESS | 6 | -0.55 | -1.10 | 0.389 | 0.797 | 1.000 | 4151 | tags=33%, list=20%, signal=42% | |
1344 | MITOCHONDRIAL TRNA MODIFICATION | 6 | -0.55 | -1.10 | 0.389 | 0.796 | 1.000 | 4151 | tags=33%, list=20%, signal=42% | |
1345 | MITOCHONDRIAL RNA MODIFICATION | 6 | -0.55 | -1.10 | 0.389 | 0.796 | 1.000 | 4151 | tags=33%, list=20%, signal=42% | |
1346 | DETECTION OF LIGHT STIMULUS INVOLVED IN VISUAL PERCEPTION | 8 | -0.47 | -1.10 | 0.347 | 0.795 | 1.000 | 6568 | tags=75%, list=32%, signal=110% | |
1347 | DETECTION OF LIGHT STIMULUS INVOLVED IN SENSORY PERCEPTION | 8 | -0.47 | -1.10 | 0.347 | 0.795 | 1.000 | 6568 | tags=75%, list=32%, signal=110% | |
1348 | DETERMINATION OF LEFT/RIGHT SYMMETRY | 103 | -0.25 | -1.10 | 0.294 | 0.794 | 1.000 | 6779 | tags=39%, list=33%, signal=58% | |
1349 | POSITIVE REGULATION OF EXTRACELLULAR MATRIX DISASSEMBLY | 6 | -0.50 | -1.10 | 0.354 | 0.794 | 1.000 | 2689 | tags=33%, list=13%, signal=38% | |
1350 | REGULATION OF PHOSPHATIDYLINOSITOL 3-KINASE ACTIVITY | 23 | -0.36 | -1.10 | 0.336 | 0.794 | 1.000 | 5650 | tags=43%, list=27%, signal=60% | |
1351 | REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 25 | -0.36 | -1.09 | 0.344 | 0.795 | 1.000 | 5287 | tags=36%, list=26%, signal=48% | |
1352 | BONE MINERALIZATION | 29 | -0.32 | -1.09 | 0.340 | 0.794 | 1.000 | 5313 | tags=34%, list=26%, signal=46% | |
1353 | CEREBRAL CORTEX REGIONALIZATION | 7 | -0.53 | -1.09 | 0.392 | 0.794 | 1.000 | 2851 | tags=43%, list=14%, signal=50% | |
1354 | PROTEIN LOCALIZATION TO EXTRACELLULAR REGION | 5 | -0.53 | -1.09 | 0.360 | 0.793 | 1.000 | 5856 | tags=60%, list=28%, signal=84% | |
1355 | MAINTENANCE OF PROTEIN LOCATION IN EXTRACELLULAR REGION | 5 | -0.53 | -1.09 | 0.360 | 0.793 | 1.000 | 5856 | tags=60%, list=28%, signal=84% | |
1356 | POLYOL METABOLIC PROCESS | 53 | -0.29 | -1.09 | 0.335 | 0.794 | 1.000 | 1442 | tags=15%, list=7%, signal=16% | |
1357 | NEPHRIC DUCT DEVELOPMENT | 14 | -0.41 | -1.09 | 0.355 | 0.793 | 1.000 | 7204 | tags=64%, list=35%, signal=99% | |
1358 | NEGATIVE REGULATION OF HORMONE SECRETION | 24 | -0.37 | -1.09 | 0.357 | 0.795 | 1.000 | 3580 | tags=33%, list=17%, signal=40% | |
1359 | CYTOSKELETAL ANCHORING AT PLASMA MEMBRANE | 5 | -0.51 | -1.09 | 0.372 | 0.795 | 1.000 | 4519 | tags=60%, list=22%, signal=77% | |
1360 | REGULATION OF BETA-AMYLOID CLEARANCE | 6 | -0.50 | -1.09 | 0.358 | 0.795 | 1.000 | 6176 | tags=50%, list=30%, signal=71% | |
1361 | WOUND HEALING, SPREADING OF EPIDERMAL CELLS | 9 | -0.45 | -1.09 | 0.340 | 0.797 | 1.000 | 5311 | tags=44%, list=26%, signal=60% | |
1362 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO VASCULAR ENDOTHELIAL GROWTH FACTOR STIMULUS | 5 | -0.58 | -1.09 | 0.405 | 0.797 | 1.000 | 7022 | tags=80%, list=34%, signal=121% | |
1363 | ASTROCYTE DIFFERENTIATION | 36 | -0.29 | -1.09 | 0.346 | 0.796 | 1.000 | 3574 | tags=25%, list=17%, signal=30% | |
1364 | NEGATIVE REGULATION OF AXON GUIDANCE | 10 | -0.42 | -1.09 | 0.364 | 0.796 | 1.000 | 7038 | tags=60%, list=34%, signal=91% | |
1365 | GAS TRANSPORT | 6 | -0.58 | -1.09 | 0.420 | 0.796 | 1.000 | 8641 | tags=100%, list=42%, signal=172% | |
1366 | PROGESTERONE METABOLIC PROCESS | 9 | -0.51 | -1.09 | 0.373 | 0.795 | 1.000 | 2655 | tags=33%, list=13%, signal=38% | |
1367 | TRABECULA MORPHOGENESIS | 37 | -0.31 | -1.09 | 0.337 | 0.795 | 1.000 | 3818 | tags=27%, list=19%, signal=33% | |
1368 | INORGANIC CATION TRANSMEMBRANE TRANSPORT | 302 | -0.25 | -1.09 | 0.331 | 0.796 | 1.000 | 6086 | tags=35%, list=30%, signal=50% | |
1369 | RESPONSE TO CARBOHYDRATE | 43 | -0.27 | -1.09 | 0.309 | 0.795 | 1.000 | 6939 | tags=42%, list=34%, signal=63% | |
1370 | LYMPH VESSEL MORPHOGENESIS | 13 | -0.39 | -1.09 | 0.343 | 0.795 | 1.000 | 6736 | tags=54%, list=33%, signal=80% | |
1371 | ASSOCIATIVE LEARNING | 13 | -0.41 | -1.09 | 0.370 | 0.795 | 1.000 | 7686 | tags=62%, list=37%, signal=98% | |
1372 | SECOND-MESSENGER-MEDIATED SIGNALING | 83 | -0.26 | -1.09 | 0.313 | 0.795 | 1.000 | 4007 | tags=28%, list=19%, signal=34% | |
1373 | MYELIN ASSEMBLY | 12 | -0.40 | -1.09 | 0.307 | 0.795 | 1.000 | 4576 | tags=42%, list=22%, signal=54% | |
1374 | REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 67 | -0.29 | -1.09 | 0.314 | 0.796 | 1.000 | 6245 | tags=37%, list=30%, signal=53% | |
1375 | ACTIVATION OF PHOSPHOLIPASE C ACTIVITY | 49 | -0.28 | -1.09 | 0.312 | 0.796 | 1.000 | 6582 | tags=45%, list=32%, signal=66% | |
1376 | MICROTUBULE ANCHORING | 10 | -0.45 | -1.09 | 0.354 | 0.796 | 1.000 | 4733 | tags=40%, list=23%, signal=52% | |
1377 | TYPE 2 IMMUNE RESPONSE | 7 | -0.46 | -1.09 | 0.329 | 0.796 | 1.000 | 4557 | tags=29%, list=22%, signal=37% | |
1378 | INTRACELLULAR STEROL TRANSPORT | 5 | -0.54 | -1.09 | 0.381 | 0.796 | 1.000 | 227 | tags=20%, list=1%, signal=20% | |
1379 | INTRACELLULAR CHOLESTEROL TRANSPORT | 5 | -0.54 | -1.09 | 0.381 | 0.795 | 1.000 | 227 | tags=20%, list=1%, signal=20% | |
1380 | NEGATIVE REGULATION OF AXON EXTENSION | 22 | -0.36 | -1.09 | 0.329 | 0.795 | 1.000 | 7038 | tags=45%, list=34%, signal=69% | |
1381 | TYPE B PANCREATIC CELL DEVELOPMENT | 13 | -0.38 | -1.09 | 0.360 | 0.795 | 1.000 | 4850 | tags=31%, list=24%, signal=40% | |
1382 | REGULATION OF DOPAMINERGIC NEURON DIFFERENTIATION | 7 | -0.47 | -1.09 | 0.363 | 0.796 | 1.000 | 2803 | tags=43%, list=14%, signal=50% | |
1383 | ACTIN-MEDIATED CELL CONTRACTION | 64 | -0.30 | -1.09 | 0.349 | 0.797 | 1.000 | 1002 | tags=13%, list=5%, signal=13% | |
1384 | NADH REGENERATION | 25 | -0.37 | -1.09 | 0.368 | 0.797 | 1.000 | 4394 | tags=28%, list=21%, signal=36% | |
1385 | GLYCOLYTIC PROCESS THROUGH FRUCTOSE-6-PHOSPHATE | 25 | -0.37 | -1.09 | 0.368 | 0.796 | 1.000 | 4394 | tags=28%, list=21%, signal=36% | |
1386 | GLYCOLYTIC PROCESS THROUGH GLUCOSE-6-PHOSPHATE | 25 | -0.37 | -1.09 | 0.368 | 0.796 | 1.000 | 4394 | tags=28%, list=21%, signal=36% | |
1387 | CANONICAL GLYCOLYSIS | 25 | -0.37 | -1.09 | 0.368 | 0.795 | 1.000 | 4394 | tags=28%, list=21%, signal=36% | |
1388 | GLUCOSE CATABOLIC PROCESS TO PYRUVATE | 25 | -0.37 | -1.09 | 0.368 | 0.795 | 1.000 | 4394 | tags=28%, list=21%, signal=36% | |
1389 | GLYCEROPHOSPHOLIPID CATABOLIC PROCESS | 6 | -0.51 | -1.09 | 0.357 | 0.794 | 1.000 | 1200 | tags=33%, list=6%, signal=35% | |
1390 | NEGATIVE REGULATION OF PROTEIN ACETYLATION | 11 | -0.43 | -1.09 | 0.382 | 0.794 | 1.000 | 4940 | tags=36%, list=24%, signal=48% | |
1391 | BIOTIN METABOLIC PROCESS | 11 | -0.43 | -1.09 | 0.382 | 0.794 | 1.000 | 1103 | tags=18%, list=5%, signal=19% | |
1392 | ORGANIC HYDROXY COMPOUND METABOLIC PROCESS | 281 | -0.24 | -1.09 | 0.304 | 0.794 | 1.000 | 5066 | tags=27%, list=25%, signal=35% | |
1393 | POSITIVE REGULATION OF RECEPTOR BIOSYNTHETIC PROCESS | 8 | -0.45 | -1.09 | 0.362 | 0.794 | 1.000 | 4506 | tags=50%, list=22%, signal=64% | |
1394 | MONOCARBOXYLIC ACID TRANSPORT | 72 | -0.28 | -1.09 | 0.333 | 0.794 | 1.000 | 3494 | tags=26%, list=17%, signal=32% | |
1395 | HEART FIELD SPECIFICATION | 7 | -0.46 | -1.09 | 0.373 | 0.794 | 1.000 | 2805 | tags=43%, list=14%, signal=50% | |
1396 | SECONDARY HEART FIELD SPECIFICATION | 7 | -0.46 | -1.09 | 0.373 | 0.793 | 1.000 | 2805 | tags=43%, list=14%, signal=50% | |
1397 | MULTICELLULAR ORGANISMAL MACROMOLECULE METABOLIC PROCESS | 65 | -0.31 | -1.09 | 0.352 | 0.793 | 1.000 | 5912 | tags=45%, list=29%, signal=62% | |
1398 | PH ELEVATION | 6 | -0.48 | -1.09 | 0.363 | 0.793 | 1.000 | 3587 | tags=33%, list=17%, signal=40% | |
1399 | INTRACELLULAR PH ELEVATION | 6 | -0.48 | -1.09 | 0.363 | 0.792 | 1.000 | 3587 | tags=33%, list=17%, signal=40% | |
1400 | BODY MORPHOGENESIS | 47 | -0.28 | -1.09 | 0.310 | 0.792 | 1.000 | 3134 | tags=21%, list=15%, signal=25% | |
1401 | REGULATION OF FAT CELL DIFFERENTIATION | 49 | -0.30 | -1.09 | 0.330 | 0.792 | 1.000 | 7698 | tags=47%, list=37%, signal=75% | |
1402 | NEGATIVE REGULATION OF FATTY ACID BIOSYNTHETIC PROCESS | 7 | -0.46 | -1.08 | 0.344 | 0.794 | 1.000 | 3155 | tags=43%, list=15%, signal=51% | |
1403 | DICARBOXYLIC ACID CATABOLIC PROCESS | 12 | -0.40 | -1.08 | 0.354 | 0.794 | 1.000 | 2765 | tags=33%, list=13%, signal=38% | |
1404 | TRIGLYCERIDE METABOLIC PROCESS | 74 | -0.28 | -1.08 | 0.322 | 0.794 | 1.000 | 4751 | tags=34%, list=23%, signal=44% | |
1405 | REGULATION OF PHOSPHATIDYLINOSITOL BIOSYNTHETIC PROCESS | 5 | -0.54 | -1.08 | 0.382 | 0.794 | 1.000 | 718 | tags=20%, list=3%, signal=21% | |
1406 | POSITIVE REGULATION OF MYELOID LEUKOCYTE DIFFERENTIATION | 25 | -0.30 | -1.08 | 0.339 | 0.795 | 1.000 | 3742 | tags=24%, list=18%, signal=29% | |
1407 | REGULATION OF NEUROGENESIS | 475 | -0.22 | -1.08 | 0.291 | 0.797 | 1.000 | 6427 | tags=36%, list=31%, signal=51% | |
1408 | REGULATION OF SEQUESTERING OF CALCIUM ION | 69 | -0.27 | -1.08 | 0.309 | 0.797 | 1.000 | 5630 | tags=35%, list=27%, signal=48% | |
1409 | SOMITOGENESIS | 52 | -0.28 | -1.08 | 0.343 | 0.797 | 1.000 | 3469 | tags=23%, list=17%, signal=28% | |
1410 | CALCIUM-DEPENDENT CELL-CELL ADHESION VIA PLASMA MEMBRANE CELL ADHESION MOLECULES | 5 | -0.53 | -1.08 | 0.378 | 0.798 | 1.000 | 7371 | tags=80%, list=36%, signal=125% | |
1411 | POSITIVE REGULATION OF STRIATED MUSCLE TISSUE DEVELOPMENT | 25 | -0.33 | -1.08 | 0.365 | 0.797 | 1.000 | 7577 | tags=48%, list=37%, signal=76% | |
1412 | POSITIVE REGULATION OF MUSCLE ORGAN DEVELOPMENT | 25 | -0.33 | -1.08 | 0.365 | 0.797 | 1.000 | 7577 | tags=48%, list=37%, signal=76% | |
1413 | NEGATIVE REGULATION OF GLUCOSE TRANSPORT | 6 | -0.52 | -1.08 | 0.385 | 0.796 | 1.000 | 4896 | tags=50%, list=24%, signal=66% | |
1414 | SYNAPTIC VESICLE CYCLE | 25 | -0.35 | -1.08 | 0.350 | 0.796 | 1.000 | 3091 | tags=28%, list=15%, signal=33% | |
1415 | POSITIVE REGULATION OF MACROPHAGE DERIVED FOAM CELL DIFFERENTIATION | 10 | -0.43 | -1.08 | 0.337 | 0.796 | 1.000 | 2358 | tags=30%, list=11%, signal=34% | |
1416 | CARDIAC MUSCLE TISSUE DEVELOPMENT | 121 | -0.25 | -1.08 | 0.333 | 0.797 | 1.000 | 5630 | tags=35%, list=27%, signal=47% | |
1417 | EPITHELIAL CELL DIFFERENTIATION | 428 | -0.23 | -1.08 | 0.302 | 0.796 | 1.000 | 5865 | tags=36%, list=28%, signal=49% | |
1418 | REGULATION OF GLYCOPROTEIN BIOSYNTHETIC PROCESS | 20 | -0.33 | -1.08 | 0.352 | 0.797 | 1.000 | 5601 | tags=45%, list=27%, signal=62% | |
1419 | REGULATION OF EXTRACELLULAR MATRIX ASSEMBLY | 8 | -0.42 | -1.08 | 0.372 | 0.797 | 1.000 | 7353 | tags=63%, list=36%, signal=97% | |
1420 | REGULATION OF CHEMOTAXIS | 108 | -0.28 | -1.08 | 0.344 | 0.797 | 1.000 | 2138 | tags=18%, list=10%, signal=20% | |
1421 | BRANCHING INVOLVED IN SALIVARY GLAND MORPHOGENESIS | 18 | -0.37 | -1.08 | 0.402 | 0.797 | 1.000 | 4336 | tags=44%, list=21%, signal=56% | |
1422 | REGULATION OF FAT CELL PROLIFERATION | 5 | -0.56 | -1.08 | 0.400 | 0.797 | 1.000 | 577 | tags=40%, list=3%, signal=41% | |
1423 | NEGATIVE REGULATION OF FAT CELL PROLIFERATION | 5 | -0.56 | -1.08 | 0.400 | 0.797 | 1.000 | 577 | tags=40%, list=3%, signal=41% | |
1424 | CENTRAL NERVOUS SYSTEM NEURON DEVELOPMENT | 63 | -0.29 | -1.08 | 0.364 | 0.797 | 1.000 | 5587 | tags=37%, list=27%, signal=50% | |
1425 | REGULATION OF CYTOSOLIC CALCIUM ION CONCENTRATION | 104 | -0.26 | -1.08 | 0.328 | 0.797 | 1.000 | 7820 | tags=49%, list=38%, signal=79% | |
1426 | EXTRACELLULAR FIBRIL ORGANIZATION | 9 | -0.48 | -1.08 | 0.390 | 0.797 | 1.000 | 3531 | tags=44%, list=17%, signal=54% | |
1427 | INOSITOL LIPID-MEDIATED SIGNALING | 111 | -0.24 | -1.08 | 0.304 | 0.797 | 1.000 | 4636 | tags=28%, list=22%, signal=36% | |
1428 | HEART TRABECULA MORPHOGENESIS | 23 | -0.34 | -1.08 | 0.353 | 0.799 | 1.000 | 7047 | tags=48%, list=34%, signal=73% | |
1429 | STEM CELL DIVISION | 20 | -0.33 | -1.08 | 0.337 | 0.798 | 1.000 | 2748 | tags=20%, list=13%, signal=23% | |
1430 | FATTY ACID BETA-OXIDATION USING ACYL-COA DEHYDROGENASE | 8 | -0.48 | -1.08 | 0.394 | 0.798 | 1.000 | 1810 | tags=25%, list=9%, signal=27% | |
1431 | PHOSPHATIDYLINOSITOL-MEDIATED SIGNALING | 110 | -0.24 | -1.08 | 0.299 | 0.799 | 1.000 | 4636 | tags=28%, list=22%, signal=36% | |
1432 | REGULATION OF CATENIN IMPORT INTO NUCLEUS | 17 | -0.36 | -1.08 | 0.359 | 0.799 | 1.000 | 8323 | tags=59%, list=40%, signal=99% | |
1433 | BROWN FAT CELL DIFFERENTIATION | 31 | -0.33 | -1.08 | 0.362 | 0.798 | 1.000 | 6654 | tags=48%, list=32%, signal=71% | |
1434 | REGULATION OF MUSCLE CELL DIFFERENTIATION | 84 | -0.28 | -1.08 | 0.365 | 0.798 | 1.000 | 5776 | tags=39%, list=28%, signal=54% | |
1435 | POSITIVE REGULATION OF CELL DEVELOPMENT | 316 | -0.23 | -1.08 | 0.311 | 0.798 | 1.000 | 4116 | tags=24%, list=20%, signal=29% | |
1436 | NEGATIVE REGULATION OF ALPHA-BETA T CELL DIFFERENTIATION | 9 | -0.41 | -1.08 | 0.337 | 0.797 | 1.000 | 3650 | tags=44%, list=18%, signal=54% | |
1437 | POSITIVE REGULATION BY HOST OF VIRAL PROCESS | 10 | -0.40 | -1.08 | 0.378 | 0.797 | 1.000 | 1357 | tags=20%, list=7%, signal=21% | |
1438 | POSITIVE REGULATION OF EMBRYONIC DEVELOPMENT | 25 | -0.31 | -1.08 | 0.375 | 0.797 | 1.000 | 6442 | tags=44%, list=31%, signal=64% | |
1439 | REGULATION OF SMOOTH MUSCLE CELL MIGRATION | 24 | -0.36 | -1.08 | 0.363 | 0.796 | 1.000 | 2138 | tags=29%, list=10%, signal=33% | |
1440 | UNSATURATED FATTY ACID BIOSYNTHETIC PROCESS | 33 | -0.32 | -1.07 | 0.349 | 0.797 | 1.000 | 2623 | tags=21%, list=13%, signal=24% | |
1441 | POSITIVE REGULATION OF NEUROGENESIS | 258 | -0.23 | -1.07 | 0.339 | 0.797 | 1.000 | 4116 | tags=25%, list=20%, signal=31% | |
1442 | GLAND DEVELOPMENT | 341 | -0.23 | -1.07 | 0.300 | 0.799 | 1.000 | 4914 | tags=27%, list=24%, signal=35% | |
1443 | CELLULAR RESPONSE TO GLUCAGON STIMULUS | 32 | -0.30 | -1.07 | 0.337 | 0.799 | 1.000 | 6582 | tags=44%, list=32%, signal=64% | |
1444 | WNT SIGNALING PATHWAY | 73 | -0.26 | -1.07 | 0.324 | 0.799 | 1.000 | 5708 | tags=37%, list=28%, signal=51% | |
1445 | DETECTION OF MECHANICAL STIMULUS | 12 | -0.40 | -1.07 | 0.377 | 0.799 | 1.000 | 5039 | tags=42%, list=24%, signal=55% | |
1446 | ORGANIC ACID TRANSPORT | 165 | -0.26 | -1.07 | 0.333 | 0.799 | 1.000 | 3494 | tags=23%, list=17%, signal=28% | |
1447 | POSITIVE REGULATION OF HEART CONTRACTION | 17 | -0.38 | -1.07 | 0.414 | 0.801 | 1.000 | 6935 | tags=59%, list=34%, signal=89% | |
1448 | CELLULAR RESPONSE TO VITAMIN | 6 | -0.50 | -1.07 | 0.383 | 0.801 | 1.000 | 1345 | tags=33%, list=7%, signal=36% | |
1449 | ANION TRANSMEMBRANE TRANSPORT | 153 | -0.25 | -1.07 | 0.344 | 0.801 | 1.000 | 2728 | tags=18%, list=13%, signal=21% | |
1450 | DENDRITE MORPHOGENESIS | 49 | -0.28 | -1.07 | 0.339 | 0.800 | 1.000 | 3647 | tags=27%, list=18%, signal=32% | |
1451 | GLIAL CELL DEVELOPMENT | 69 | -0.26 | -1.07 | 0.360 | 0.801 | 1.000 | 5302 | tags=29%, list=26%, signal=39% | |
1452 | REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 38 | -0.33 | -1.07 | 0.376 | 0.803 | 1.000 | 3534 | tags=29%, list=17%, signal=35% | |
1453 | POSITIVE REGULATION OF CYCLIN-DEPENDENT PROTEIN KINASE ACTIVITY | 19 | -0.34 | -1.07 | 0.368 | 0.803 | 1.000 | 7022 | tags=58%, list=34%, signal=88% | |
1454 | NEGATIVE REGULATION OF MYELOID LEUKOCYTE DIFFERENTIATION | 22 | -0.36 | -1.07 | 0.354 | 0.803 | 1.000 | 3937 | tags=32%, list=19%, signal=39% | |
1455 | ARTERY DEVELOPMENT | 74 | -0.28 | -1.07 | 0.356 | 0.804 | 1.000 | 4380 | tags=31%, list=21%, signal=39% | |
1456 | BRANCHIOMOTOR NEURON AXON GUIDANCE | 5 | -0.51 | -1.07 | 0.407 | 0.804 | 1.000 | 6400 | tags=60%, list=31%, signal=87% | |
1457 | DETERMINATION OF LEFT/RIGHT ASYMMETRY IN LATERAL MESODERM | 5 | -0.55 | -1.07 | 0.431 | 0.804 | 1.000 | 4600 | tags=80%, list=22%, signal=103% | |
1458 | POSITIVE REGULATION OF CYCLIN-DEPENDENT PROTEIN SERINE/THREONINE KINASE ACTIVITY | 17 | -0.35 | -1.07 | 0.359 | 0.803 | 1.000 | 7022 | tags=59%, list=34%, signal=89% | |
1459 | ANTERIOR/POSTERIOR AXIS SPECIFICATION | 41 | -0.31 | -1.07 | 0.360 | 0.804 | 1.000 | 7031 | tags=51%, list=34%, signal=78% | |
1460 | REGULATION OF EPITHELIAL CELL PROLIFERATION | 147 | -0.25 | -1.07 | 0.329 | 0.804 | 1.000 | 6245 | tags=35%, list=30%, signal=50% | |
1461 | FLAVONOID METABOLIC PROCESS | 5 | -0.53 | -1.07 | 0.413 | 0.806 | 1.000 | 3000 | tags=40%, list=15%, signal=47% | |
1462 | ICOSANOID BIOSYNTHETIC PROCESS | 26 | -0.34 | -1.07 | 0.337 | 0.806 | 1.000 | 2623 | tags=23%, list=13%, signal=26% | |
1463 | FATTY ACID DERIVATIVE BIOSYNTHETIC PROCESS | 26 | -0.34 | -1.07 | 0.337 | 0.805 | 1.000 | 2623 | tags=23%, list=13%, signal=26% | |
1464 | NEGATIVE REGULATION OF LYMPHOCYTE MIGRATION | 5 | -0.53 | -1.07 | 0.389 | 0.805 | 1.000 | 26 | tags=20%, list=0%, signal=20% | |
1465 | SEGMENTATION | 74 | -0.26 | -1.07 | 0.357 | 0.805 | 1.000 | 3680 | tags=23%, list=18%, signal=28% | |
1466 | EQUILIBRIOCEPTION | 5 | -0.53 | -1.07 | 0.430 | 0.805 | 1.000 | 7959 | tags=60%, list=39%, signal=98% | |
1467 | GOLGI DISASSEMBLY | 5 | -0.52 | -1.07 | 0.383 | 0.807 | 1.000 | 2025 | tags=40%, list=10%, signal=44% | |
1468 | COFACTOR TRANSPORT | 13 | -0.38 | -1.07 | 0.364 | 0.807 | 1.000 | 2661 | tags=31%, list=13%, signal=35% | |
1469 | MUCOPOLYSACCHARIDE METABOLIC PROCESS | 80 | -0.28 | -1.07 | 0.369 | 0.807 | 1.000 | 4496 | tags=30%, list=22%, signal=38% | |
1470 | REGULATION OF BEHAVIOR | 126 | -0.27 | -1.07 | 0.352 | 0.806 | 1.000 | 3202 | tags=21%, list=16%, signal=24% | |
1471 | NEPHRON DEVELOPMENT | 109 | -0.26 | -1.06 | 0.363 | 0.806 | 1.000 | 4557 | tags=29%, list=22%, signal=37% | |
1472 | POSTSYNAPTIC MEMBRANE ASSEMBLY | 8 | -0.46 | -1.06 | 0.395 | 0.806 | 1.000 | 6147 | tags=50%, list=30%, signal=71% | |
1473 | REGULATION OF KERATINOCYTE PROLIFERATION | 14 | -0.39 | -1.06 | 0.378 | 0.806 | 1.000 | 3815 | tags=36%, list=19%, signal=44% | |
1474 | NEGATIVE REGULATION OF INTRACELLULAR STEROID HORMONE RECEPTOR SIGNALING PATHWAY | 27 | -0.32 | -1.06 | 0.353 | 0.807 | 1.000 | 4506 | tags=33%, list=22%, signal=43% | |
1475 | SMOOTH MUSCLE CONTRACTION | 24 | -0.35 | -1.06 | 0.373 | 0.807 | 1.000 | 6719 | tags=46%, list=33%, signal=68% | |
1476 | REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 81 | -0.26 | -1.06 | 0.374 | 0.807 | 1.000 | 4049 | tags=23%, list=20%, signal=29% | |
1477 | COCHLEA DEVELOPMENT | 36 | -0.33 | -1.06 | 0.393 | 0.806 | 1.000 | 5804 | tags=39%, list=28%, signal=54% | |
1478 | NEGATIVE REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 18 | -0.38 | -1.06 | 0.393 | 0.807 | 1.000 | 3560 | tags=39%, list=17%, signal=47% | |
1479 | POSITIVE REGULATION OF CELL MIGRATION BY VASCULAR ENDOTHELIAL GROWTH FACTOR SIGNALING PATHWAY | 5 | -0.52 | -1.06 | 0.412 | 0.807 | 1.000 | 7282 | tags=60%, list=35%, signal=93% | |
1480 | BRAINSTEM DEVELOPMENT | 5 | -0.52 | -1.06 | 0.411 | 0.807 | 1.000 | 2052 | tags=40%, list=10%, signal=44% | |
1481 | DETERMINATION OF ADULT LIFESPAN | 17 | -0.35 | -1.06 | 0.369 | 0.807 | 1.000 | 3210 | tags=24%, list=16%, signal=28% | |
1482 | POSITIVE REGULATION OF CYTOSOLIC CALCIUM ION CONCENTRATION | 94 | -0.26 | -1.06 | 0.339 | 0.807 | 1.000 | 5630 | tags=33%, list=27%, signal=45% | |
1483 | CARDIAC MUSCLE CELL PROLIFERATION | 12 | -0.42 | -1.06 | 0.396 | 0.807 | 1.000 | 395 | tags=17%, list=2%, signal=17% | |
1484 | ENDOTHELIAL CELL MORPHOGENESIS | 10 | -0.40 | -1.06 | 0.379 | 0.811 | 1.000 | 7586 | tags=60%, list=37%, signal=95% | |
1485 | RESPONSE TO MAGNESIUM ION | 6 | -0.51 | -1.06 | 0.394 | 0.811 | 1.000 | 5990 | tags=67%, list=29%, signal=94% | |
1486 | REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 40 | -0.30 | -1.06 | 0.357 | 0.811 | 1.000 | 3961 | tags=28%, list=19%, signal=34% | |
1487 | POSITIVE REGULATION OF CYTOSKELETON ORGANIZATION | 105 | -0.25 | -1.06 | 0.351 | 0.811 | 1.000 | 2964 | tags=21%, list=14%, signal=24% | |
1488 | DNA DAMAGE RESPONSE, SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR RESULTING IN TRANSCRIPTION OF P21 CLASS MEDIATOR | 10 | -0.42 | -1.06 | 0.385 | 0.811 | 1.000 | 2492 | tags=30%, list=12%, signal=34% | |
1489 | CEREBRAL CORTEX RADIALLY ORIENTED CELL MIGRATION | 29 | -0.32 | -1.06 | 0.368 | 0.812 | 1.000 | 743 | tags=14%, list=4%, signal=14% | |
1490 | DETERMINATION OF DIGESTIVE TRACT LEFT/RIGHT ASYMMETRY | 5 | -0.49 | -1.06 | 0.379 | 0.813 | 1.000 | 427 | tags=20%, list=2%, signal=20% | |
1491 | NEGATIVE REGULATION OF ALPHA-BETA T CELL ACTIVATION | 14 | -0.39 | -1.06 | 0.396 | 0.813 | 1.000 | 3650 | tags=36%, list=18%, signal=43% | |
1492 | TYPE B PANCREATIC CELL DIFFERENTIATION | 16 | -0.35 | -1.06 | 0.403 | 0.812 | 1.000 | 6710 | tags=38%, list=33%, signal=56% | |
1493 | REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR SIGNALING PATHWAY | 9 | -0.43 | -1.06 | 0.414 | 0.813 | 1.000 | 9433 | tags=78%, list=46%, signal=143% | |
1494 | CORONARY VASCULATURE DEVELOPMENT | 38 | -0.31 | -1.06 | 0.388 | 0.813 | 1.000 | 2805 | tags=26%, list=14%, signal=30% | |
1495 | NEGATIVE REGULATION OF PROTEIN ACTIVATION CASCADE | 9 | -0.46 | -1.06 | 0.407 | 0.812 | 1.000 | 5376 | tags=56%, list=26%, signal=75% | |
1496 | THALAMUS DEVELOPMENT | 10 | -0.43 | -1.06 | 0.414 | 0.812 | 1.000 | 4688 | tags=50%, list=23%, signal=65% | |
1497 | GLANDULAR EPITHELIAL CELL DIFFERENTIATION | 37 | -0.32 | -1.06 | 0.387 | 0.815 | 1.000 | 5357 | tags=35%, list=26%, signal=47% | |
1498 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 89 | -0.24 | -1.06 | 0.371 | 0.815 | 1.000 | 4940 | tags=28%, list=24%, signal=37% | |
1499 | CELLULAR MODIFIED AMINO ACID CATABOLIC PROCESS | 7 | -0.46 | -1.06 | 0.397 | 0.814 | 1.000 | 4643 | tags=43%, list=23%, signal=55% | |
1500 | MESENCHYME DEVELOPMENT | 165 | -0.24 | -1.06 | 0.369 | 0.814 | 1.000 | 7048 | tags=42%, list=34%, signal=63% | |
1501 | MULTICELLULAR ORGANISMAL MOVEMENT | 18 | -0.38 | -1.06 | 0.384 | 0.815 | 1.000 | 7719 | tags=61%, list=37%, signal=98% | |
1502 | MUSCULOSKELETAL MOVEMENT | 18 | -0.38 | -1.06 | 0.384 | 0.814 | 1.000 | 7719 | tags=61%, list=37%, signal=98% | |
1503 | VOCALIZATION BEHAVIOR | 11 | -0.46 | -1.06 | 0.427 | 0.814 | 1.000 | 6120 | tags=55%, list=30%, signal=78% | |
1504 | VASOCONSTRICTION | 9 | -0.40 | -1.05 | 0.387 | 0.816 | 1.000 | 6719 | tags=56%, list=33%, signal=82% | |
1505 | SPERM-EGG RECOGNITION | 18 | -0.35 | -1.05 | 0.398 | 0.816 | 1.000 | 6010 | tags=50%, list=29%, signal=71% | |
1506 | REGULATION OF IMMUNOGLOBULIN MEDIATED IMMUNE RESPONSE | 16 | -0.36 | -1.05 | 0.373 | 0.816 | 1.000 | 7979 | tags=56%, list=39%, signal=92% | |
1507 | MITOCHONDRIAL RNA PROCESSING | 12 | -0.47 | -1.05 | 0.448 | 0.816 | 1.000 | 1532 | tags=25%, list=7%, signal=27% | |
1508 | CELL VOLUME HOMEOSTASIS | 8 | -0.46 | -1.05 | 0.393 | 0.816 | 1.000 | 4787 | tags=38%, list=23%, signal=49% | |
1509 | PERICARDIUM MORPHOGENESIS | 7 | -0.45 | -1.05 | 0.391 | 0.816 | 1.000 | 6710 | tags=57%, list=33%, signal=85% | |
1510 | SENSORY PERCEPTION OF CHEMICAL STIMULUS | 46 | -0.33 | -1.05 | 0.418 | 0.816 | 1.000 | 7095 | tags=50%, list=34%, signal=76% | |
1511 | FOREBRAIN REGIONALIZATION | 20 | -0.41 | -1.05 | 0.416 | 0.816 | 1.000 | 6181 | tags=45%, list=30%, signal=64% | |
1512 | MEMBRANE LIPID CATABOLIC PROCESS | 12 | -0.42 | -1.05 | 0.415 | 0.816 | 1.000 | 1577 | tags=33%, list=8%, signal=36% | |
1513 | REGULATION OF NEURON MIGRATION | 23 | -0.36 | -1.05 | 0.394 | 0.816 | 1.000 | 1213 | tags=17%, list=6%, signal=18% | |
1514 | BRANCHING MORPHOGENESIS OF AN EPITHELIAL TUBE | 148 | -0.23 | -1.05 | 0.361 | 0.816 | 1.000 | 5173 | tags=30%, list=25%, signal=40% | |
1515 | SKELETAL MUSCLE THIN FILAMENT ASSEMBLY | 5 | -0.53 | -1.05 | 0.424 | 0.817 | 1.000 | 4823 | tags=40%, list=23%, signal=52% | |
1516 | TRACHEA DEVELOPMENT | 19 | -0.35 | -1.05 | 0.400 | 0.818 | 1.000 | 3217 | tags=32%, list=16%, signal=37% | |
1517 | NEPHRON EPITHELIUM DEVELOPMENT | 85 | -0.26 | -1.05 | 0.359 | 0.818 | 1.000 | 4557 | tags=31%, list=22%, signal=39% | |
1518 | MATURE B CELL DIFFERENTIATION INVOLVED IN IMMUNE RESPONSE | 14 | -0.35 | -1.05 | 0.376 | 0.818 | 1.000 | 4047 | tags=36%, list=20%, signal=44% | |
1519 | LUNG CELL DIFFERENTIATION | 29 | -0.31 | -1.05 | 0.392 | 0.817 | 1.000 | 4761 | tags=45%, list=23%, signal=58% | |
1520 | POSITIVE REGULATION OF BEHAVIOR | 81 | -0.29 | -1.05 | 0.398 | 0.818 | 1.000 | 3202 | tags=23%, list=16%, signal=28% | |
1521 | GROWTH PLATE CARTILAGE DEVELOPMENT | 14 | -0.41 | -1.05 | 0.428 | 0.817 | 1.000 | 4745 | tags=50%, list=23%, signal=65% | |
1522 | ANDROGEN METABOLIC PROCESS | 15 | -0.35 | -1.05 | 0.399 | 0.817 | 1.000 | 2803 | tags=27%, list=14%, signal=31% | |
1523 | NEUROMUSCULAR PROCESS CONTROLLING BALANCE | 10 | -0.41 | -1.05 | 0.419 | 0.818 | 1.000 | 7959 | tags=60%, list=39%, signal=98% | |
1524 | CARDIAC RIGHT VENTRICLE MORPHOGENESIS | 15 | -0.37 | -1.05 | 0.393 | 0.819 | 1.000 | 4557 | tags=33%, list=22%, signal=43% | |
1525 | MYELINATION | 71 | -0.25 | -1.05 | 0.366 | 0.818 | 1.000 | 3524 | tags=24%, list=17%, signal=29% | |
1526 | REGULATION OF MONOOXYGENASE ACTIVITY | 48 | -0.30 | -1.05 | 0.381 | 0.819 | 1.000 | 7138 | tags=42%, list=35%, signal=64% | |
1527 | NEGATIVE REGULATION OF CELL CYCLE ARREST | 14 | -0.40 | -1.05 | 0.424 | 0.819 | 1.000 | 3839 | tags=36%, list=19%, signal=44% | |
1528 | NEURON PROJECTION EXTENSION | 47 | -0.29 | -1.05 | 0.385 | 0.819 | 1.000 | 7038 | tags=45%, list=34%, signal=68% | |
1529 | REGULATION OF MONONUCLEAR CELL MIGRATION | 7 | -0.51 | -1.05 | 0.444 | 0.820 | 1.000 | 7076 | tags=57%, list=34%, signal=87% | |
1530 | REGULATION OF PLATELET ACTIVATION | 21 | -0.36 | -1.05 | 0.410 | 0.819 | 1.000 | 6961 | tags=52%, list=34%, signal=79% | |
1531 | INDOLE-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 5 | -0.53 | -1.05 | 0.432 | 0.819 | 1.000 | 5010 | tags=40%, list=24%, signal=53% | |
1532 | INDOLALKYLAMINE BIOSYNTHETIC PROCESS | 5 | -0.53 | -1.05 | 0.432 | 0.819 | 1.000 | 5010 | tags=40%, list=24%, signal=53% | |
1533 | POSITIVE REGULATION OF ANTIGEN RECEPTOR-MEDIATED SIGNALING PATHWAY | 6 | -0.47 | -1.05 | 0.426 | 0.818 | 1.000 | 2994 | tags=33%, list=15%, signal=39% | |
1534 | LUNG EPITHELIAL CELL DIFFERENTIATION | 28 | -0.31 | -1.05 | 0.398 | 0.820 | 1.000 | 4761 | tags=46%, list=23%, signal=60% | |
1535 | NEGATIVE REGULATION OF PATHWAY-RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 8 | -0.44 | -1.05 | 0.389 | 0.819 | 1.000 | 4281 | tags=38%, list=21%, signal=47% | |
1536 | POSITIVE REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 28 | -0.31 | -1.05 | 0.396 | 0.819 | 1.000 | 3238 | tags=18%, list=16%, signal=21% | |
1537 | REGULATION OF ACTIVATION OF JAK2 KINASE ACTIVITY | 6 | -0.49 | -1.05 | 0.447 | 0.819 | 1.000 | 3574 | tags=33%, list=17%, signal=40% | |
1538 | NADH METABOLIC PROCESS | 26 | -0.35 | -1.05 | 0.419 | 0.820 | 1.000 | 4394 | tags=27%, list=21%, signal=34% | |
1539 | REGULATION OF CELL MORPHOGENESIS | 340 | -0.22 | -1.04 | 0.341 | 0.821 | 1.000 | 5312 | tags=30%, list=26%, signal=40% | |
1540 | HISTONE H3-K36 METHYLATION | 6 | -0.50 | -1.04 | 0.444 | 0.821 | 1.000 | 7272 | tags=67%, list=35%, signal=103% | |
1541 | ENDOCHONDRAL BONE MORPHOGENESIS | 47 | -0.30 | -1.04 | 0.408 | 0.821 | 1.000 | 4850 | tags=38%, list=24%, signal=50% | |
1542 | FEEDING BEHAVIOR | 24 | -0.34 | -1.04 | 0.400 | 0.821 | 1.000 | 6410 | tags=42%, list=31%, signal=60% | |
1543 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION OF SMELL | 5 | -0.52 | -1.04 | 0.436 | 0.821 | 1.000 | 8966 | tags=80%, list=44%, signal=142% | |
1544 | CALCIUM-MEDIATED SIGNALING | 52 | -0.26 | -1.04 | 0.385 | 0.821 | 1.000 | 2830 | tags=21%, list=14%, signal=24% | |
1545 | GLUCONEOGENESIS | 37 | -0.31 | -1.04 | 0.401 | 0.824 | 1.000 | 4394 | tags=22%, list=21%, signal=27% | |
1546 | REGULATION OF ANGIOTENSIN LEVELS IN BLOOD | 13 | -0.42 | -1.04 | 0.400 | 0.824 | 1.000 | 3574 | tags=38%, list=17%, signal=47% | |
1547 | REGULATION OF ANGIOTENSIN METABOLIC PROCESS | 13 | -0.42 | -1.04 | 0.400 | 0.823 | 1.000 | 3574 | tags=38%, list=17%, signal=47% | |
1548 | MUSCLE CELL CELLULAR HOMEOSTASIS | 11 | -0.40 | -1.04 | 0.405 | 0.825 | 1.000 | 8391 | tags=64%, list=41%, signal=107% | |
1549 | REGULATION OF CELL PROJECTION ORGANIZATION | 341 | -0.22 | -1.04 | 0.365 | 0.825 | 1.000 | 6431 | tags=37%, list=31%, signal=53% | |
1550 | REGULATION OF METANEPHRIC GLOMERULUS DEVELOPMENT | 6 | -0.50 | -1.04 | 0.427 | 0.826 | 1.000 | 2544 | tags=33%, list=12%, signal=38% | |
1551 | HEXOSE BIOSYNTHETIC PROCESS | 39 | -0.31 | -1.04 | 0.401 | 0.826 | 1.000 | 4394 | tags=21%, list=21%, signal=26% | |
1552 | NEGATIVE REGULATION OF CYTOKINE SECRETION INVOLVED IN IMMUNE RESPONSE | 5 | -0.52 | -1.04 | 0.448 | 0.825 | 1.000 | 444 | tags=20%, list=2%, signal=20% | |
1553 | CRISTAE FORMATION | 6 | -0.50 | -1.04 | 0.453 | 0.825 | 1.000 | 4878 | tags=50%, list=24%, signal=65% | |
1554 | DEVELOPMENT OF PRIMARY SEXUAL CHARACTERISTICS | 151 | -0.22 | -1.04 | 0.356 | 0.825 | 1.000 | 2385 | tags=16%, list=12%, signal=18% | |
1555 | REGULATION OF MUSCLE SYSTEM PROCESS | 104 | -0.26 | -1.04 | 0.383 | 0.825 | 1.000 | 5327 | tags=36%, list=26%, signal=48% | |
1556 | HORMONE-MEDIATED SIGNALING PATHWAY | 31 | -0.30 | -1.04 | 0.406 | 0.824 | 1.000 | 4914 | tags=32%, list=24%, signal=42% | |
1557 | OVARIAN FOLLICLE DEVELOPMENT | 38 | -0.27 | -1.04 | 0.358 | 0.825 | 1.000 | 4689 | tags=32%, list=23%, signal=41% | |
1558 | SECRETION | 299 | -0.24 | -1.04 | 0.374 | 0.824 | 1.000 | 3293 | tags=22%, list=16%, signal=26% | |
1559 | NEGATIVE REGULATION OF LIPOPROTEIN LIPASE ACTIVITY | 5 | -0.56 | -1.04 | 0.450 | 0.824 | 1.000 | 3155 | tags=60%, list=15%, signal=71% | |
1560 | NEGATIVE REGULATION OF B CELL MEDIATED IMMUNITY | 6 | -0.48 | -1.04 | 0.410 | 0.824 | 1.000 | 7979 | tags=83%, list=39%, signal=136% | |
1561 | NEGATIVE REGULATION OF IMMUNOGLOBULIN MEDIATED IMMUNE RESPONSE | 6 | -0.48 | -1.04 | 0.410 | 0.823 | 1.000 | 7979 | tags=83%, list=39%, signal=136% | |
1562 | POSITIVE REGULATION OF PROTEIN TYROSINE KINASE ACTIVITY | 28 | -0.31 | -1.04 | 0.419 | 0.823 | 1.000 | 6094 | tags=39%, list=30%, signal=56% | |
1563 | REGULATION OF DOPAMINE UPTAKE INVOLVED IN SYNAPTIC TRANSMISSION | 5 | -0.50 | -1.04 | 0.440 | 0.827 | 1.000 | 6144 | tags=60%, list=30%, signal=85% | |
1564 | REGULATION OF CATECHOLAMINE UPTAKE INVOLVED IN SYNAPTIC TRANSMISSION | 5 | -0.50 | -1.04 | 0.440 | 0.827 | 1.000 | 6144 | tags=60%, list=30%, signal=85% | |
1565 | REGULATION OF GLOMERULAR MESANGIAL CELL PROLIFERATION | 5 | -0.54 | -1.04 | 0.424 | 0.827 | 1.000 | 1523 | tags=40%, list=7%, signal=43% | |
1566 | POSITIVE REGULATION OF FIBROBLAST PROLIFERATION | 26 | -0.34 | -1.04 | 0.409 | 0.827 | 1.000 | 3961 | tags=31%, list=19%, signal=38% | |
1567 | NEGATIVE REGULATION OF MUSCLE TISSUE DEVELOPMENT | 18 | -0.38 | -1.04 | 0.430 | 0.826 | 1.000 | 5287 | tags=39%, list=26%, signal=52% | |
1568 | REGULATION OF KERATINOCYTE DIFFERENTIATION | 16 | -0.33 | -1.04 | 0.409 | 0.826 | 1.000 | 2781 | tags=31%, list=13%, signal=36% | |
1569 | NEGATIVE REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 22 | -0.34 | -1.04 | 0.412 | 0.826 | 1.000 | 3312 | tags=27%, list=16%, signal=32% | |
1570 | POSITIVE REGULATION OF MACROPHAGE DIFFERENTIATION | 8 | -0.43 | -1.04 | 0.420 | 0.827 | 1.000 | 3580 | tags=38%, list=17%, signal=45% | |
1571 | EAR DEVELOPMENT | 200 | -0.24 | -1.04 | 0.407 | 0.826 | 1.000 | 6504 | tags=37%, list=32%, signal=53% | |
1572 | RESPONSE TO CADMIUM ION | 9 | -0.56 | -1.04 | 0.473 | 0.826 | 1.000 | 176 | tags=22%, list=1%, signal=22% | |
1573 | PLATELET ACTIVATION | 203 | -0.26 | -1.04 | 0.387 | 0.826 | 1.000 | 3246 | tags=21%, list=16%, signal=25% | |
1574 | PROTEIN HOMOTRIMERIZATION | 9 | -0.44 | -1.04 | 0.414 | 0.826 | 1.000 | 2535 | tags=33%, list=12%, signal=38% | |
1575 | BIOLOGICAL PHASE | 15 | -0.38 | -1.04 | 0.400 | 0.826 | 1.000 | 4628 | tags=47%, list=22%, signal=60% | |
1576 | NITRIC OXIDE METABOLIC PROCESS | 24 | -0.32 | -1.04 | 0.393 | 0.826 | 1.000 | 4304 | tags=25%, list=21%, signal=32% | |
1577 | POSITIVE REGULATION OF MACROPHAGE CHEMOTAXIS | 5 | -0.56 | -1.04 | 0.456 | 0.826 | 1.000 | 7076 | tags=60%, list=34%, signal=91% | |
1578 | NEURAL PLATE MORPHOGENESIS | 7 | -0.50 | -1.03 | 0.458 | 0.826 | 1.000 | 5600 | tags=57%, list=27%, signal=78% | |
1579 | NEGATIVE REGULATION OF PHAGOCYTOSIS | 5 | -0.48 | -1.03 | 0.416 | 0.826 | 1.000 | 2480 | tags=20%, list=12%, signal=23% | |
1580 | REGULATION OF PEPTIDE HORMONE SECRETION | 120 | -0.23 | -1.03 | 0.371 | 0.825 | 1.000 | 6031 | tags=28%, list=29%, signal=40% | |
1581 | REGULATION OF T CELL TOLERANCE INDUCTION | 7 | -0.47 | -1.03 | 0.438 | 0.827 | 1.000 | 2493 | tags=29%, list=12%, signal=32% | |
1582 | POSITIVE REGULATION OF PHOSPHATIDYLINOSITOL 3-KINASE SIGNALING | 44 | -0.29 | -1.03 | 0.402 | 0.827 | 1.000 | 5650 | tags=39%, list=27%, signal=53% | |
1583 | NEGATIVE T CELL SELECTION | 14 | -0.40 | -1.03 | 0.425 | 0.827 | 1.000 | 3650 | tags=43%, list=18%, signal=52% | |
1584 | NEGATIVE THYMIC T CELL SELECTION | 14 | -0.40 | -1.03 | 0.425 | 0.826 | 1.000 | 3650 | tags=43%, list=18%, signal=52% | |
1585 | REGULATION OF KETONE BIOSYNTHETIC PROCESS | 8 | -0.45 | -1.03 | 0.440 | 0.826 | 1.000 | 5050 | tags=50%, list=25%, signal=66% | |
1586 | RESPONSE TO SUPEROXIDE | 7 | -0.47 | -1.03 | 0.420 | 0.826 | 1.000 | 8337 | tags=57%, list=40%, signal=96% | |
1587 | REMOVAL OF SUPEROXIDE RADICALS | 7 | -0.47 | -1.03 | 0.420 | 0.825 | 1.000 | 8337 | tags=57%, list=40%, signal=96% | |
1588 | CELLULAR RESPONSE TO OXYGEN RADICAL | 7 | -0.47 | -1.03 | 0.420 | 0.825 | 1.000 | 8337 | tags=57%, list=40%, signal=96% | |
1589 | CELLULAR RESPONSE TO SUPEROXIDE | 7 | -0.47 | -1.03 | 0.420 | 0.824 | 1.000 | 8337 | tags=57%, list=40%, signal=96% | |
1590 | REGULATION OF CARDIAC CONDUCTION | 60 | -0.27 | -1.03 | 0.415 | 0.824 | 1.000 | 4269 | tags=30%, list=21%, signal=38% | |
1591 | REGULATION OF PEPTIDE SECRETION | 121 | -0.23 | -1.03 | 0.388 | 0.824 | 1.000 | 6031 | tags=28%, list=29%, signal=39% | |
1592 | TEMPERATURE HOMEOSTASIS | 7 | -0.47 | -1.03 | 0.423 | 0.824 | 1.000 | 3690 | tags=43%, list=18%, signal=52% | |
1593 | POSITIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 274 | -0.22 | -1.03 | 0.408 | 0.824 | 1.000 | 6395 | tags=36%, list=31%, signal=52% | |
1594 | RETINAL BLOOD VESSEL MORPHOGENESIS | 5 | -0.53 | -1.03 | 0.448 | 0.824 | 1.000 | 6424 | tags=60%, list=31%, signal=87% | |
1595 | NEGATIVE REGULATION OF NUCLEOTIDE BIOSYNTHETIC PROCESS | 23 | -0.33 | -1.03 | 0.429 | 0.824 | 1.000 | 5264 | tags=43%, list=26%, signal=58% | |
1596 | NEGATIVE REGULATION OF PURINE NUCLEOTIDE BIOSYNTHETIC PROCESS | 23 | -0.33 | -1.03 | 0.429 | 0.823 | 1.000 | 5264 | tags=43%, list=26%, signal=58% | |
1597 | CONVERGENT EXTENSION INVOLVED IN AXIS ELONGATION | 7 | -0.47 | -1.03 | 0.472 | 0.827 | 1.000 | 1192 | tags=29%, list=6%, signal=30% | |
1598 | NEGATIVE REGULATION OF VITAMIN D BIOSYNTHETIC PROCESS | 5 | -0.52 | -1.03 | 0.457 | 0.827 | 1.000 | 4753 | tags=40%, list=23%, signal=52% | |
1599 | POSITIVE REGULATION OF NEUROTRANSMITTER TRANSPORT | 7 | -0.46 | -1.03 | 0.456 | 0.829 | 1.000 | 3494 | tags=43%, list=17%, signal=52% | |
1600 | REGULATION OF TRIGLYCERIDE METABOLIC PROCESS | 15 | -0.41 | -1.03 | 0.439 | 0.831 | 1.000 | 4193 | tags=40%, list=20%, signal=50% | |
1601 | MECHANORECEPTOR DIFFERENTIATION | 64 | -0.26 | -1.03 | 0.414 | 0.831 | 1.000 | 5804 | tags=38%, list=28%, signal=52% | |
1602 | WNT SIGNALING PATHWAY INVOLVED IN HEART DEVELOPMENT | 5 | -0.50 | -1.03 | 0.428 | 0.830 | 1.000 | 6710 | tags=60%, list=33%, signal=89% | |
1603 | REGULATION OF CELL PROLIFERATION INVOLVED IN KIDNEY DEVELOPMENT | 8 | -0.45 | -1.03 | 0.436 | 0.830 | 1.000 | 5650 | tags=63%, list=27%, signal=86% | |
1604 | ROSTROCAUDAL NEURAL TUBE PATTERNING | 11 | -0.42 | -1.03 | 0.429 | 0.830 | 1.000 | 7208 | tags=55%, list=35%, signal=84% | |
1605 | CARBOHYDRATE BIOSYNTHETIC PROCESS | 74 | -0.26 | -1.03 | 0.402 | 0.831 | 1.000 | 4394 | tags=22%, list=21%, signal=27% | |
1606 | REGULATION OF LAMELLIPODIUM ASSEMBLY | 13 | -0.40 | -1.03 | 0.461 | 0.833 | 1.000 | 6599 | tags=46%, list=32%, signal=68% | |
1607 | REGULATION OF NEUROTRANSMITTER UPTAKE | 9 | -0.39 | -1.03 | 0.408 | 0.833 | 1.000 | 3494 | tags=22%, list=17%, signal=27% | |
1608 | HEART DEVELOPMENT | 430 | -0.20 | -1.03 | 0.358 | 0.832 | 1.000 | 5657 | tags=29%, list=27%, signal=40% | |
1609 | REGULATION OF INTERLEUKIN-12 SECRETION | 5 | -0.50 | -1.03 | 0.439 | 0.832 | 1.000 | 3293 | tags=40%, list=16%, signal=48% | |
1610 | PHOSPHATIDYLSERINE METABOLIC PROCESS | 21 | -0.33 | -1.03 | 0.428 | 0.832 | 1.000 | 5479 | tags=38%, list=27%, signal=52% | |
1611 | CHONDROITIN SULFATE BIOSYNTHETIC PROCESS | 13 | -0.41 | -1.03 | 0.420 | 0.834 | 1.000 | 3412 | tags=38%, list=17%, signal=46% | |
1612 | STRIATED MUSCLE CELL PROLIFERATION | 13 | -0.40 | -1.03 | 0.450 | 0.833 | 1.000 | 395 | tags=15%, list=2%, signal=16% | |
1613 | POSITIVE REGULATION OF ISOTYPE SWITCHING | 6 | -0.47 | -1.03 | 0.439 | 0.833 | 1.000 | 4961 | tags=50%, list=24%, signal=66% | |
1614 | CARDIAC CHAMBER DEVELOPMENT | 148 | -0.23 | -1.03 | 0.412 | 0.833 | 1.000 | 3327 | tags=22%, list=16%, signal=26% | |
1615 | NEGATIVE REGULATION OF HUMORAL IMMUNE RESPONSE | 9 | -0.44 | -1.02 | 0.433 | 0.835 | 1.000 | 7979 | tags=78%, list=39%, signal=127% | |
1616 | REGULATION OF CGMP METABOLIC PROCESS | 12 | -0.41 | -1.02 | 0.441 | 0.834 | 1.000 | 6848 | tags=67%, list=33%, signal=100% | |
1617 | RENAL SYSTEM VASCULATURE DEVELOPMENT | 16 | -0.37 | -1.02 | 0.427 | 0.834 | 1.000 | 4259 | tags=50%, list=21%, signal=63% | |
1618 | KIDNEY VASCULATURE DEVELOPMENT | 16 | -0.37 | -1.02 | 0.427 | 0.833 | 1.000 | 4259 | tags=50%, list=21%, signal=63% | |
1619 | REGULATION OF GLIOGENESIS | 59 | -0.26 | -1.02 | 0.409 | 0.833 | 1.000 | 5503 | tags=32%, list=27%, signal=44% | |
1620 | NEGATIVE REGULATION OF CELL GROWTH | 107 | -0.25 | -1.02 | 0.409 | 0.833 | 1.000 | 6710 | tags=39%, list=33%, signal=58% | |
1621 | SENSORY PERCEPTION | 196 | -0.27 | -1.02 | 0.423 | 0.833 | 1.000 | 6755 | tags=42%, list=33%, signal=62% | |
1622 | LYMPHOCYTE APOPTOTIC PROCESS | 7 | -0.46 | -1.02 | 0.425 | 0.833 | 1.000 | 3650 | tags=43%, list=18%, signal=52% | |
1623 | RESPONSE TO CGMP | 5 | -0.48 | -1.02 | 0.451 | 0.833 | 1.000 | 793 | tags=40%, list=4%, signal=42% | |
1624 | CELLULAR RESPONSE TO CGMP | 5 | -0.48 | -1.02 | 0.451 | 0.832 | 1.000 | 793 | tags=40%, list=4%, signal=42% | |
1625 | REGULATION OF SEQUENCE-SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 278 | -0.23 | -1.02 | 0.413 | 0.832 | 1.000 | 5439 | tags=29%, list=26%, signal=40% | |
1626 | HEMOSTASIS | 453 | -0.23 | -1.02 | 0.379 | 0.832 | 1.000 | 3560 | tags=21%, list=17%, signal=25% | |
1627 | REGULATION OF CELL SIZE | 89 | -0.25 | -1.02 | 0.425 | 0.832 | 1.000 | 2653 | tags=18%, list=13%, signal=21% | |
1628 | PALATE DEVELOPMENT | 80 | -0.26 | -1.02 | 0.436 | 0.831 | 1.000 | 5465 | tags=35%, list=27%, signal=47% | |
1629 | RESPONSE TO LAMINAR FLUID SHEAR STRESS | 10 | -0.44 | -1.02 | 0.432 | 0.831 | 1.000 | 1637 | tags=30%, list=8%, signal=33% | |
1630 | POSITIVE REGULATION OF EPITHELIAL CELL PROLIFERATION INVOLVED IN WOUND HEALING | 5 | -0.48 | -1.02 | 0.451 | 0.831 | 1.000 | 8585 | tags=60%, list=42%, signal=103% | |
1631 | CALCIUM-MEDIATED SIGNALING USING INTRACELLULAR CALCIUM SOURCE | 11 | -0.40 | -1.02 | 0.426 | 0.831 | 1.000 | 7881 | tags=45%, list=38%, signal=74% | |
1632 | DNA STRAND RENATURATION | 8 | -0.47 | -1.02 | 0.453 | 0.831 | 1.000 | 7639 | tags=63%, list=37%, signal=99% | |
1633 | MAMMARY GLAND EPITHELIUM DEVELOPMENT | 62 | -0.27 | -1.02 | 0.421 | 0.832 | 1.000 | 5050 | tags=31%, list=25%, signal=40% | |
1634 | POSITIVE REGULATION OF EXTRACELLULAR MATRIX ASSEMBLY | 6 | -0.47 | -1.02 | 0.459 | 0.832 | 1.000 | 7353 | tags=67%, list=36%, signal=104% | |
1635 | DNA DAMAGE RESPONSE, SIGNAL TRANSDUCTION RESULTING IN TRANSCRIPTION | 11 | -0.40 | -1.02 | 0.455 | 0.832 | 1.000 | 2492 | tags=27%, list=12%, signal=31% | |
1636 | RESPONSE TO GONADOTROPIN | 6 | -0.50 | -1.02 | 0.451 | 0.832 | 1.000 | 3717 | tags=50%, list=18%, signal=61% | |
1637 | POTASSIUM ION EXPORT | 7 | -0.46 | -1.02 | 0.440 | 0.832 | 1.000 | 5327 | tags=57%, list=26%, signal=77% | |
1638 | REGULATION OF THE FORCE OF HEART CONTRACTION | 14 | -0.36 | -1.02 | 0.436 | 0.832 | 1.000 | 6719 | tags=43%, list=33%, signal=64% | |
1639 | PLATELET-DERIVED GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 15 | -0.36 | -1.02 | 0.425 | 0.832 | 1.000 | 5650 | tags=47%, list=27%, signal=64% | |
1640 | COLLAGEN CATABOLIC PROCESS | 60 | -0.30 | -1.02 | 0.439 | 0.832 | 1.000 | 5912 | tags=45%, list=29%, signal=63% | |
1641 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 76 | -0.27 | -1.02 | 0.413 | 0.833 | 1.000 | 5023 | tags=30%, list=24%, signal=40% | |
1642 | REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 76 | -0.27 | -1.02 | 0.413 | 0.833 | 1.000 | 5023 | tags=30%, list=24%, signal=40% | |
1643 | DEPYRIMIDINATION | 8 | -0.45 | -1.02 | 0.430 | 0.833 | 1.000 | 2575 | tags=38%, list=12%, signal=43% | |
1644 | SENSORY PERCEPTION OF LIGHT STIMULUS | 83 | -0.28 | -1.02 | 0.436 | 0.833 | 1.000 | 6755 | tags=43%, list=33%, signal=64% | |
1645 | POSITIVE REGULATION OF VASOCONSTRICTION | 7 | -0.49 | -1.02 | 0.469 | 0.834 | 1.000 | 5243 | tags=57%, list=25%, signal=77% | |
1646 | HYALURONAN BIOSYNTHETIC PROCESS | 6 | -0.48 | -1.02 | 0.456 | 0.835 | 1.000 | 4496 | tags=33%, list=22%, signal=43% | |
1647 | DEVELOPMENTAL PROCESS INVOLVED IN REPRODUCTION | 499 | -0.20 | -1.02 | 0.414 | 0.834 | 1.000 | 5650 | tags=30%, list=27%, signal=40% | |
1648 | CRANIAL NERVE FORMATION | 5 | -0.48 | -1.02 | 0.453 | 0.834 | 1.000 | 9238 | tags=60%, list=45%, signal=109% | |
1649 | ENDOCHONDRAL BONE GROWTH | 19 | -0.39 | -1.02 | 0.459 | 0.834 | 1.000 | 6071 | tags=53%, list=29%, signal=75% | |
1650 | POSITIVE REGULATION OF URINE VOLUME | 7 | -0.49 | -1.02 | 0.492 | 0.834 | 1.000 | 153 | tags=14%, list=1%, signal=14% | |
1651 | MULTI-ORGANISM REPRODUCTIVE PROCESS | 376 | -0.20 | -1.02 | 0.414 | 0.834 | 1.000 | 6048 | tags=33%, list=29%, signal=45% | |
1652 | FEMALE GAMETE GENERATION | 59 | -0.24 | -1.02 | 0.394 | 0.834 | 1.000 | 5215 | tags=32%, list=25%, signal=43% | |
1653 | AMINO-ACID BETAINE TRANSPORT | 13 | -0.40 | -1.02 | 0.450 | 0.833 | 1.000 | 1103 | tags=23%, list=5%, signal=24% | |
1654 | CARNITINE TRANSPORT | 13 | -0.40 | -1.02 | 0.450 | 0.833 | 1.000 | 1103 | tags=23%, list=5%, signal=24% | |
1655 | MEMBRANE PROTEIN PROTEOLYSIS | 29 | -0.33 | -1.02 | 0.458 | 0.833 | 1.000 | 3172 | tags=28%, list=15%, signal=33% | |
1656 | RESPONSE TO HISTAMINE | 9 | -0.41 | -1.02 | 0.456 | 0.833 | 1.000 | 10078 | tags=67%, list=49%, signal=130% | |
1657 | NEGATIVE REGULATION OF NEUROTRANSMITTER TRANSPORT | 6 | -0.46 | -1.02 | 0.464 | 0.833 | 1.000 | 160 | tags=17%, list=1%, signal=17% | |
1658 | ORGANIC HYDROXY COMPOUND CATABOLIC PROCESS | 28 | -0.32 | -1.02 | 0.421 | 0.833 | 1.000 | 4924 | tags=39%, list=24%, signal=52% | |
1659 | TUBE MORPHOGENESIS | 347 | -0.21 | -1.02 | 0.405 | 0.833 | 1.000 | 5186 | tags=27%, list=25%, signal=36% | |
1660 | BLOOD COAGULATION | 449 | -0.23 | -1.02 | 0.393 | 0.834 | 1.000 | 3560 | tags=21%, list=17%, signal=24% | |
1661 | REGULATION OF NATURAL KILLER CELL MEDIATED IMMUNITY | 25 | -0.32 | -1.01 | 0.449 | 0.835 | 1.000 | 3208 | tags=20%, list=16%, signal=24% | |
1662 | REGULATION OF PHOSPHOLIPID CATABOLIC PROCESS | 5 | -0.51 | -1.01 | 0.463 | 0.834 | 1.000 | 3581 | tags=40%, list=17%, signal=48% | |
1663 | MONOTERPENOID METABOLIC PROCESS | 6 | -0.46 | -1.01 | 0.462 | 0.835 | 1.000 | 5651 | tags=67%, list=27%, signal=92% | |
1664 | GERM-LINE STEM CELL POPULATION MAINTENANCE | 6 | -0.46 | -1.01 | 0.454 | 0.834 | 1.000 | 907 | tags=33%, list=4%, signal=35% | |
1665 | NEGATIVE REGULATION OF BEHAVIOR | 29 | -0.31 | -1.01 | 0.442 | 0.835 | 1.000 | 2062 | tags=21%, list=10%, signal=23% | |
1666 | ADP METABOLIC PROCESS | 28 | -0.34 | -1.01 | 0.434 | 0.836 | 1.000 | 4394 | tags=25%, list=21%, signal=32% | |
1667 | CARNITINE TRANSMEMBRANE TRANSPORT | 12 | -0.41 | -1.01 | 0.452 | 0.836 | 1.000 | 1103 | tags=25%, list=5%, signal=26% | |
1668 | REGULATION OF THYMOCYTE APOPTOTIC PROCESS | 7 | -0.45 | -1.01 | 0.454 | 0.835 | 1.000 | 1523 | tags=14%, list=7%, signal=15% | |
1669 | HEART MORPHOGENESIS | 213 | -0.22 | -1.01 | 0.395 | 0.835 | 1.000 | 4380 | tags=24%, list=21%, signal=30% | |
1670 | REGULATION OF LYMPHOCYTE DIFFERENTIATION | 59 | -0.25 | -1.01 | 0.425 | 0.835 | 1.000 | 5743 | tags=36%, list=28%, signal=49% | |
1671 | POSITIVE REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 35 | -0.29 | -1.01 | 0.461 | 0.836 | 1.000 | 3534 | tags=26%, list=17%, signal=31% | |
1672 | REGULATION OF CILIUM MOVEMENT | 7 | -0.42 | -1.01 | 0.461 | 0.836 | 1.000 | 9303 | tags=71%, list=45%, signal=130% | |
1673 | REGULATION OF PROTEIN POLYUBIQUITINATION | 8 | -0.42 | -1.01 | 0.441 | 0.836 | 1.000 | 7446 | tags=50%, list=36%, signal=78% | |
1674 | LUNG ALVEOLUS DEVELOPMENT | 47 | -0.27 | -1.01 | 0.441 | 0.836 | 1.000 | 3815 | tags=30%, list=19%, signal=36% | |
1675 | PALLIUM DEVELOPMENT | 123 | -0.23 | -1.01 | 0.416 | 0.836 | 1.000 | 5383 | tags=28%, list=26%, signal=37% | |
1676 | MITOCHONDRIAL CALCIUM ION HOMEOSTASIS | 7 | -0.45 | -1.01 | 0.447 | 0.836 | 1.000 | 8315 | tags=57%, list=40%, signal=96% | |
1677 | NEGATIVE REGULATION OF STRIATED MUSCLE CELL APOPTOTIC PROCESS | 5 | -0.49 | -1.01 | 0.461 | 0.836 | 1.000 | 8867 | tags=80%, list=43%, signal=140% | |
1678 | EPITHELIAL TUBE MORPHOGENESIS | 310 | -0.20 | -1.01 | 0.408 | 0.837 | 1.000 | 5186 | tags=28%, list=25%, signal=37% | |
1679 | VASCULAR PROCESS IN CIRCULATORY SYSTEM | 55 | -0.28 | -1.01 | 0.435 | 0.837 | 1.000 | 3574 | tags=27%, list=17%, signal=33% | |
1680 | GANGLION DEVELOPMENT | 13 | -0.35 | -1.01 | 0.432 | 0.837 | 1.000 | 3105 | tags=23%, list=15%, signal=27% | |
1681 | RECEPTOR GUANYLYL CYCLASE SIGNALING PATHWAY | 9 | -0.46 | -1.01 | 0.479 | 0.838 | 1.000 | 153 | tags=22%, list=1%, signal=22% | |
1682 | COLLAGEN METABOLIC PROCESS | 64 | -0.29 | -1.01 | 0.442 | 0.837 | 1.000 | 5912 | tags=44%, list=29%, signal=61% | |
1683 | PYRUVATE METABOLIC PROCESS | 53 | -0.28 | -1.01 | 0.435 | 0.837 | 1.000 | 4394 | tags=30%, list=21%, signal=38% | |
1684 | DNA METHYLATION OR DEMETHYLATION | 47 | -0.26 | -1.01 | 0.437 | 0.838 | 1.000 | 7667 | tags=38%, list=37%, signal=61% | |
1685 | COAGULATION | 451 | -0.23 | -1.01 | 0.411 | 0.839 | 1.000 | 3560 | tags=21%, list=17%, signal=24% | |
1686 | CELLULAR RESPONSE TO GONADOTROPIN STIMULUS | 5 | -0.54 | -1.01 | 0.497 | 0.839 | 1.000 | 3717 | tags=60%, list=18%, signal=73% | |
1687 | NEGATIVE REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 10 | -0.42 | -1.01 | 0.450 | 0.839 | 1.000 | 7094 | tags=60%, list=34%, signal=91% | |
1688 | GONAD DEVELOPMENT | 148 | -0.22 | -1.01 | 0.458 | 0.842 | 1.000 | 2385 | tags=16%, list=12%, signal=17% | |
1689 | CATECHOL-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 11 | -0.42 | -1.01 | 0.494 | 0.842 | 1.000 | 9594 | tags=73%, list=47%, signal=136% | |
1690 | CATECHOLAMINE BIOSYNTHETIC PROCESS | 11 | -0.42 | -1.01 | 0.494 | 0.842 | 1.000 | 9594 | tags=73%, list=47%, signal=136% | |
1691 | MONOVALENT INORGANIC CATION TRANSPORT | 232 | -0.24 | -1.01 | 0.455 | 0.842 | 1.000 | 6086 | tags=33%, list=30%, signal=47% | |
1692 | REGULATION OF DIGESTIVE SYSTEM PROCESS | 10 | -0.40 | -1.01 | 0.451 | 0.841 | 1.000 | 5926 | tags=50%, list=29%, signal=70% | |
1693 | ERK1 AND ERK2 CASCADE | 13 | -0.36 | -1.01 | 0.441 | 0.841 | 1.000 | 5505 | tags=46%, list=27%, signal=63% | |
1694 | REGULATION OF PHOSPHOLIPASE A2 ACTIVITY | 6 | -0.47 | -1.01 | 0.481 | 0.841 | 1.000 | 2494 | tags=33%, list=12%, signal=38% | |
1695 | ORGANOPHOSPHATE ESTER TRANSPORT | 48 | -0.27 | -1.01 | 0.453 | 0.841 | 1.000 | 5620 | tags=35%, list=27%, signal=49% | |
1696 | VENOUS BLOOD VESSEL MORPHOGENESIS | 11 | -0.41 | -1.00 | 0.475 | 0.843 | 1.000 | 7204 | tags=55%, list=35%, signal=84% | |
1697 | REGULATION OF CARDIOBLAST DIFFERENTIATION | 5 | -0.52 | -1.00 | 0.477 | 0.842 | 1.000 | 4163 | tags=40%, list=20%, signal=50% | |
1698 | NEGATIVE REGULATION OF ADAPTIVE IMMUNE RESPONSE | 19 | -0.33 | -1.00 | 0.457 | 0.842 | 1.000 | 7979 | tags=63%, list=39%, signal=103% | |
1699 | REGULATION OF OXIDOREDUCTASE ACTIVITY | 70 | -0.26 | -1.00 | 0.450 | 0.842 | 1.000 | 7138 | tags=43%, list=35%, signal=65% | |
1700 | REGULATION OF LIPOPROTEIN LIPASE ACTIVITY | 11 | -0.44 | -1.00 | 0.475 | 0.842 | 1.000 | 4193 | tags=55%, list=20%, signal=68% | |
1701 | POSITIVE REGULATION OF ERK1 AND ERK2 CASCADE | 94 | -0.26 | -1.00 | 0.447 | 0.841 | 1.000 | 5825 | tags=36%, list=28%, signal=50% | |
1702 | REGULATION OF REMOVAL OF SUPEROXIDE RADICALS | 5 | -0.49 | -1.00 | 0.450 | 0.841 | 1.000 | 7708 | tags=80%, list=37%, signal=128% | |
1703 | EMBRYONIC AXIS SPECIFICATION | 29 | -0.29 | -1.00 | 0.449 | 0.841 | 1.000 | 6710 | tags=45%, list=33%, signal=66% | |
1704 | RESPONSE TO MACROPHAGE COLONY-STIMULATING FACTOR | 5 | -0.49 | -1.00 | 0.457 | 0.841 | 1.000 | 5155 | tags=60%, list=25%, signal=80% | |
1705 | CELLULAR RESPONSE TO MACROPHAGE COLONY-STIMULATING FACTOR STIMULUS | 5 | -0.49 | -1.00 | 0.457 | 0.841 | 1.000 | 5155 | tags=60%, list=25%, signal=80% | |
1706 | GAMMA-DELTA T CELL ACTIVATION | 5 | -0.49 | -1.00 | 0.462 | 0.841 | 1.000 | 3858 | tags=40%, list=19%, signal=49% | |
1707 | POSITIVE REGULATION OF BLOOD CIRCULATION | 30 | -0.33 | -1.00 | 0.471 | 0.841 | 1.000 | 5630 | tags=43%, list=27%, signal=60% | |
1708 | IRE1-MEDIATED UNFOLDED PROTEIN RESPONSE | 53 | -0.31 | -1.00 | 0.459 | 0.841 | 1.000 | 3344 | tags=26%, list=16%, signal=31% | |
1709 | IONOTROPIC GLUTAMATE RECEPTOR SIGNALING PATHWAY | 20 | -0.33 | -1.00 | 0.453 | 0.840 | 1.000 | 7964 | tags=65%, list=39%, signal=106% | |
1710 | POSITIVE REGULATION OF CALCIUM ION TRANSPORT | 55 | -0.28 | -1.00 | 0.453 | 0.842 | 1.000 | 5854 | tags=38%, list=28%, signal=53% | |
1711 | TRANSMISSION OF NERVE IMPULSE | 14 | -0.36 | -1.00 | 0.439 | 0.841 | 1.000 | 7755 | tags=57%, list=38%, signal=92% | |
1712 | RESPONSE TO EXOGENOUS DSRNA | 11 | -0.42 | -1.00 | 0.459 | 0.841 | 1.000 | 3689 | tags=45%, list=18%, signal=55% | |
1713 | REGULATION OF MUSCLE TISSUE DEVELOPMENT | 46 | -0.27 | -1.00 | 0.432 | 0.842 | 1.000 | 6442 | tags=39%, list=31%, signal=57% | |
1714 | CELLULAR RESPONSE TO PLATELET-DERIVED GROWTH FACTOR STIMULUS | 7 | -0.48 | -1.00 | 0.482 | 0.841 | 1.000 | 5493 | tags=57%, list=27%, signal=78% | |
1715 | POSITIVE REGULATION OF LYMPHOCYTE DIFFERENTIATION | 38 | -0.28 | -1.00 | 0.452 | 0.841 | 1.000 | 5743 | tags=39%, list=28%, signal=55% | |
1716 | LONG-CHAIN FATTY ACID METABOLIC PROCESS | 68 | -0.28 | -1.00 | 0.454 | 0.841 | 1.000 | 5590 | tags=35%, list=27%, signal=48% | |
1717 | CELLULAR DEFENSE RESPONSE | 48 | -0.29 | -1.00 | 0.427 | 0.841 | 1.000 | 5246 | tags=38%, list=25%, signal=50% | |
1718 | NEGATIVE REGULATION OF ANION TRANSPORT | 15 | -0.37 | -1.00 | 0.470 | 0.841 | 1.000 | 1043 | tags=13%, list=5%, signal=14% | |
1719 | POSITIVE REGULATION OF CHEMOTAXIS | 76 | -0.28 | -1.00 | 0.457 | 0.841 | 1.000 | 3202 | tags=22%, list=16%, signal=26% | |
1720 | DIGESTIVE SYSTEM PROCESS | 21 | -0.34 | -1.00 | 0.478 | 0.841 | 1.000 | 5139 | tags=43%, list=25%, signal=57% | |
1721 | REGULATION OF MUSCLE ORGAN DEVELOPMENT | 47 | -0.27 | -1.00 | 0.433 | 0.841 | 1.000 | 6442 | tags=38%, list=31%, signal=56% | |
1722 | REGULATION OF TYPE B PANCREATIC CELL DEVELOPMENT | 8 | -0.42 | -1.00 | 0.440 | 0.841 | 1.000 | 2622 | tags=25%, list=13%, signal=29% | |
1723 | DETECTION OF STIMULUS INVOLVED IN SENSORY PERCEPTION | 49 | -0.32 | -1.00 | 0.469 | 0.840 | 1.000 | 7095 | tags=51%, list=34%, signal=78% | |
1724 | REGULATION OF STEM CELL PROLIFERATION | 48 | -0.28 | -1.00 | 0.458 | 0.841 | 1.000 | 3650 | tags=29%, list=18%, signal=35% | |
1725 | NEUROENDOCRINE CELL DIFFERENTIATION | 8 | -0.43 | -1.00 | 0.464 | 0.840 | 1.000 | 1192 | tags=25%, list=6%, signal=27% | |
1726 | RUFFLE ORGANIZATION | 13 | -0.39 | -1.00 | 0.481 | 0.840 | 1.000 | 1615 | tags=23%, list=8%, signal=25% | |
1727 | POSITIVE REGULATION OF IMMUNOGLOBULIN PRODUCTION | 13 | -0.36 | -1.00 | 0.476 | 0.840 | 1.000 | 5743 | tags=38%, list=28%, signal=53% | |
1728 | CELLULAR RESPONSE TO ALCOHOL | 38 | -0.29 | -1.00 | 0.464 | 0.841 | 1.000 | 1470 | tags=16%, list=7%, signal=17% | |
1729 | SECRETION BY CELL | 251 | -0.24 | -1.00 | 0.464 | 0.841 | 1.000 | 3293 | tags=22%, list=16%, signal=26% | |
1730 | CYCLOOXYGENASE PATHWAY | 10 | -0.43 | -1.00 | 0.458 | 0.841 | 1.000 | 4874 | tags=40%, list=24%, signal=52% | |
1731 | REGULATION OF PROTEIN KINASE C SIGNALING | 9 | -0.41 | -1.00 | 0.460 | 0.841 | 1.000 | 1192 | tags=22%, list=6%, signal=24% | |
1732 | REPRODUCTIVE SYSTEM DEVELOPMENT | 352 | -0.20 | -1.00 | 0.455 | 0.841 | 1.000 | 5650 | tags=31%, list=27%, signal=42% | |
1733 | CELL JUNCTION MAINTENANCE | 5 | -0.52 | -1.00 | 0.518 | 0.841 | 1.000 | 247 | tags=20%, list=1%, signal=20% | |
1734 | TAURINE METABOLIC PROCESS | 5 | -0.50 | -1.00 | 0.519 | 0.841 | 1.000 | 5608 | tags=60%, list=27%, signal=82% | |
1735 | NATURAL KILLER CELL MEDIATED IMMUNITY | 11 | -0.41 | -1.00 | 0.474 | 0.841 | 1.000 | 1595 | tags=27%, list=8%, signal=30% | |
1736 | MIDDLE EAR MORPHOGENESIS | 23 | -0.31 | -1.00 | 0.441 | 0.841 | 1.000 | 6656 | tags=48%, list=32%, signal=71% | |
1737 | NEGATIVE REGULATION OF NEUROBLAST PROLIFERATION | 5 | -0.48 | -1.00 | 0.490 | 0.841 | 1.000 | 1246 | tags=20%, list=6%, signal=21% | |
1738 | POSITIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 17 | -0.37 | -1.00 | 0.470 | 0.840 | 1.000 | 5023 | tags=47%, list=24%, signal=62% | |
1739 | POSITIVE REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 17 | -0.37 | -1.00 | 0.470 | 0.840 | 1.000 | 5023 | tags=47%, list=24%, signal=62% | |
1740 | CARDIAC SEPTUM DEVELOPMENT | 93 | -0.23 | -1.00 | 0.442 | 0.840 | 1.000 | 4823 | tags=28%, list=23%, signal=36% | |
1741 | REGULATION OF REPRODUCTIVE PROCESS | 39 | -0.29 | -1.00 | 0.466 | 0.839 | 1.000 | 6111 | tags=46%, list=30%, signal=65% | |
1742 | PYRIMIDINE-CONTAINING COMPOUND CATABOLIC PROCESS | 28 | -0.29 | -1.00 | 0.490 | 0.842 | 1.000 | 2575 | tags=21%, list=12%, signal=24% | |
1743 | POSITIVE REGULATION OF COLLAGEN METABOLIC PROCESS | 9 | -0.42 | -1.00 | 0.462 | 0.841 | 1.000 | 7097 | tags=67%, list=34%, signal=102% | |
1744 | POSITIVE REGULATION OF COLLAGEN BIOSYNTHETIC PROCESS | 9 | -0.42 | -1.00 | 0.462 | 0.841 | 1.000 | 7097 | tags=67%, list=34%, signal=102% | |
1745 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 9 | -0.42 | -1.00 | 0.462 | 0.840 | 1.000 | 7097 | tags=67%, list=34%, signal=102% | |
1746 | HYPOTHALAMUS DEVELOPMENT | 14 | -0.39 | -1.00 | 0.485 | 0.840 | 1.000 | 2518 | tags=21%, list=12%, signal=24% | |
1747 | NEGATIVE REGULATION OF CYTOKINE-MEDIATED SIGNALING PATHWAY | 21 | -0.32 | -1.00 | 0.469 | 0.841 | 1.000 | 3170 | tags=24%, list=15%, signal=28% | |
1748 | REGULATION OF SYNAPTIC TRANSMISSION, DOPAMINERGIC | 8 | -0.43 | -1.00 | 0.480 | 0.840 | 1.000 | 7577 | tags=63%, list=37%, signal=99% | |
1749 | MONOCARBOXYLIC ACID METABOLIC PROCESS | 306 | -0.22 | -0.99 | 0.447 | 0.841 | 1.000 | 4041 | tags=24%, list=20%, signal=29% | |
1750 | GLYCOSPHINGOLIPID BIOSYNTHETIC PROCESS | 11 | -0.38 | -0.99 | 0.475 | 0.841 | 1.000 | 1561 | tags=18%, list=8%, signal=20% | |
1751 | REGULATION OF PROTEIN LOCALIZATION TO SYNAPSE | 5 | -0.47 | -0.99 | 0.460 | 0.841 | 1.000 | 308 | tags=20%, list=1%, signal=20% | |
1752 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO SYNAPSE | 5 | -0.47 | -0.99 | 0.460 | 0.841 | 1.000 | 308 | tags=20%, list=1%, signal=20% | |
1753 | CELL-CELL ADHESION | 355 | -0.21 | -0.99 | 0.456 | 0.840 | 1.000 | 5515 | tags=30%, list=27%, signal=41% | |
1754 | MEGAKARYOCYTE DEVELOPMENT | 13 | -0.38 | -0.99 | 0.471 | 0.840 | 1.000 | 1038 | tags=15%, list=5%, signal=16% | |
1755 | REGULATION OF CELL GROWTH | 218 | -0.21 | -0.99 | 0.489 | 0.840 | 1.000 | 4762 | tags=24%, list=23%, signal=31% | |
1756 | PROSTANOID METABOLIC PROCESS | 18 | -0.36 | -0.99 | 0.467 | 0.841 | 1.000 | 2125 | tags=22%, list=10%, signal=25% | |
1757 | PROSTAGLANDIN METABOLIC PROCESS | 18 | -0.36 | -0.99 | 0.467 | 0.840 | 1.000 | 2125 | tags=22%, list=10%, signal=25% | |
1758 | DUCTUS ARTERIOSUS CLOSURE | 5 | -0.46 | -0.99 | 0.482 | 0.840 | 1.000 | 5287 | tags=40%, list=26%, signal=54% | |
1759 | NEGATIVE REGULATION OF PROTEIN COMPLEX ASSEMBLY | 51 | -0.26 | -0.99 | 0.478 | 0.842 | 1.000 | 1531 | tags=14%, list=7%, signal=15% | |
1760 | REGULATION OF FIBROBLAST PROLIFERATION | 41 | -0.28 | -0.99 | 0.465 | 0.841 | 1.000 | 2480 | tags=22%, list=12%, signal=25% | |
1761 | POSITIVE REGULATION OF LYMPHOCYTE ACTIVATION | 162 | -0.23 | -0.99 | 0.447 | 0.841 | 1.000 | 3879 | tags=23%, list=19%, signal=29% | |
1762 | CELLULAR COMPONENT ASSEMBLY INVOLVED IN MORPHOGENESIS | 180 | -0.22 | -0.99 | 0.469 | 0.841 | 1.000 | 5944 | tags=33%, list=29%, signal=46% | |
1763 | REGULATION OF MACROPHAGE ACTIVATION | 9 | -0.42 | -0.99 | 0.466 | 0.843 | 1.000 | 6710 | tags=56%, list=33%, signal=82% | |
1764 | INTRACILIARY TRANSPORT INVOLVED IN CILIUM MORPHOGENESIS | 6 | -0.49 | -0.99 | 0.476 | 0.843 | 1.000 | 7273 | tags=83%, list=35%, signal=129% | |
1765 | NEGATIVE REGULATION OF CELLULAR COMPONENT MOVEMENT | 161 | -0.23 | -0.99 | 0.471 | 0.843 | 1.000 | 4566 | tags=27%, list=22%, signal=35% | |
1766 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION | 33 | -0.35 | -0.99 | 0.488 | 0.843 | 1.000 | 7095 | tags=52%, list=34%, signal=78% | |
1767 | POLYOL TRANSPORT | 8 | -0.39 | -0.99 | 0.472 | 0.842 | 1.000 | 80 | tags=13%, list=0%, signal=13% | |
1768 | REGULATION OF BONE REMODELING | 16 | -0.35 | -0.99 | 0.488 | 0.842 | 1.000 | 7064 | tags=38%, list=34%, signal=57% | |
1769 | EOSINOPHIL CHEMOTAXIS | 7 | -0.45 | -0.99 | 0.495 | 0.842 | 1.000 | 7735 | tags=43%, list=38%, signal=69% | |
1770 | EOSINOPHIL MIGRATION | 7 | -0.45 | -0.99 | 0.495 | 0.842 | 1.000 | 7735 | tags=43%, list=38%, signal=69% | |
1771 | OSSIFICATION | 162 | -0.21 | -0.99 | 0.465 | 0.841 | 1.000 | 6592 | tags=36%, list=32%, signal=52% | |
1772 | NEGATIVE REGULATION OF BONE MINERALIZATION | 7 | -0.44 | -0.99 | 0.471 | 0.841 | 1.000 | 7094 | tags=71%, list=34%, signal=109% | |
1773 | NEGATIVE REGULATION OF CELL PROJECTION ORGANIZATION | 97 | -0.24 | -0.99 | 0.482 | 0.840 | 1.000 | 6710 | tags=43%, list=33%, signal=64% | |
1774 | REGULATION OF VASCULATURE DEVELOPMENT | 152 | -0.23 | -0.99 | 0.465 | 0.840 | 1.000 | 5990 | tags=34%, list=29%, signal=48% | |
1775 | REPRODUCTIVE STRUCTURE DEVELOPMENT | 349 | -0.20 | -0.99 | 0.478 | 0.841 | 1.000 | 5650 | tags=31%, list=27%, signal=42% | |
1776 | NEGATIVE REGULATION OF OXIDOREDUCTASE ACTIVITY | 20 | -0.36 | -0.99 | 0.486 | 0.841 | 1.000 | 7138 | tags=55%, list=35%, signal=84% | |
1777 | REGULATION OF HEMOPOIESIS | 144 | -0.23 | -0.99 | 0.457 | 0.841 | 1.000 | 4047 | tags=24%, list=20%, signal=30% | |
1778 | PRESYNAPTIC MEMBRANE ORGANIZATION | 10 | -0.41 | -0.99 | 0.476 | 0.841 | 1.000 | 6262 | tags=50%, list=30%, signal=72% | |
1779 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE III PROMOTER | 6 | -0.46 | -0.99 | 0.461 | 0.840 | 1.000 | 125 | tags=17%, list=1%, signal=17% | |
1780 | PURINE NUCLEOSIDE TRANSMEMBRANE TRANSPORT | 6 | -0.42 | -0.99 | 0.493 | 0.841 | 1.000 | 4393 | tags=33%, list=21%, signal=42% | |
1781 | SELENOCYSTEINE METABOLIC PROCESS | 79 | -0.34 | -0.99 | 0.496 | 0.842 | 1.000 | 10452 | tags=70%, list=51%, signal=141% | |
1782 | PHOTORECEPTOR CELL DIFFERENTIATION | 58 | -0.25 | -0.99 | 0.494 | 0.841 | 1.000 | 5650 | tags=40%, list=27%, signal=54% | |
1783 | SYNAPTIC TRANSMISSION, CHOLINERGIC | 12 | -0.36 | -0.99 | 0.495 | 0.841 | 1.000 | 9574 | tags=67%, list=46%, signal=124% | |
1784 | ACTIVATION OF PROTEIN KINASE B ACTIVITY | 14 | -0.37 | -0.99 | 0.459 | 0.842 | 1.000 | 4384 | tags=43%, list=21%, signal=54% | |
1785 | POSITIVE REGULATION OF HEART RATE | 10 | -0.37 | -0.99 | 0.483 | 0.841 | 1.000 | 3192 | tags=40%, list=15%, signal=47% | |
1786 | PEPTIDYL-TYROSINE DEPHOSPHORYLATION | 61 | -0.26 | -0.99 | 0.475 | 0.841 | 1.000 | 2836 | tags=21%, list=14%, signal=25% | |
1787 | HIPPO SIGNALING | 24 | -0.29 | -0.99 | 0.483 | 0.841 | 1.000 | 3427 | tags=29%, list=17%, signal=35% | |
1788 | PHOTORECEPTOR CELL MAINTENANCE | 21 | -0.31 | -0.99 | 0.468 | 0.840 | 1.000 | 5337 | tags=33%, list=26%, signal=45% | |
1789 | REGULATION OF APOPTOTIC CELL CLEARANCE | 6 | -0.48 | -0.99 | 0.469 | 0.841 | 1.000 | 3512 | tags=50%, list=17%, signal=60% | |
1790 | RESPONSE TO TRANSFORMING GROWTH FACTOR BETA | 133 | -0.23 | -0.99 | 0.465 | 0.840 | 1.000 | 5313 | tags=28%, list=26%, signal=37% | |
1791 | VASCULATURE DEVELOPMENT | 389 | -0.21 | -0.99 | 0.489 | 0.841 | 1.000 | 6592 | tags=36%, list=32%, signal=52% | |
1792 | NEGATIVE REGULATION OF PROTEIN PROCESSING | 20 | -0.33 | -0.99 | 0.487 | 0.841 | 1.000 | 7979 | tags=70%, list=39%, signal=114% | |
1793 | NEGATIVE REGULATION OF PROTEIN MATURATION | 20 | -0.33 | -0.99 | 0.487 | 0.840 | 1.000 | 7979 | tags=70%, list=39%, signal=114% | |
1794 | MRNA STABILIZATION | 22 | -0.29 | -0.99 | 0.455 | 0.840 | 1.000 | 577 | tags=9%, list=3%, signal=9% | |
1795 | POSITIVE REGULATION OF SYNAPSE MATURATION | 8 | -0.43 | -0.99 | 0.521 | 0.840 | 1.000 | 8089 | tags=63%, list=39%, signal=103% | |
1796 | SECONDARY ALCOHOL METABOLIC PROCESS | 52 | -0.26 | -0.99 | 0.497 | 0.840 | 1.000 | 4753 | tags=27%, list=23%, signal=35% | |
1797 | POSITIVE REGULATION OF MACROPHAGE ACTIVATION | 6 | -0.46 | -0.99 | 0.478 | 0.840 | 1.000 | 6710 | tags=67%, list=33%, signal=99% | |
1798 | SALIVARY GLAND MORPHOGENESIS | 31 | -0.30 | -0.99 | 0.496 | 0.840 | 1.000 | 4336 | tags=32%, list=21%, signal=41% | |
1799 | CELLULAR RESPONSE TO EPIDERMAL GROWTH FACTOR STIMULUS | 10 | -0.38 | -0.99 | 0.474 | 0.840 | 1.000 | 8323 | tags=60%, list=40%, signal=101% | |
1800 | EPITHELIAL CELL-CELL ADHESION | 9 | -0.45 | -0.99 | 0.467 | 0.839 | 1.000 | 4148 | tags=56%, list=20%, signal=70% | |
1801 | NEGATIVE REGULATION OF NEURON DEATH | 61 | -0.24 | -0.98 | 0.484 | 0.840 | 1.000 | 4384 | tags=26%, list=21%, signal=33% | |
1802 | PORPHYRIN-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 16 | -0.36 | -0.98 | 0.496 | 0.841 | 1.000 | 5012 | tags=31%, list=24%, signal=41% | |
1803 | TETRAPYRROLE BIOSYNTHETIC PROCESS | 16 | -0.36 | -0.98 | 0.496 | 0.840 | 1.000 | 5012 | tags=31%, list=24%, signal=41% | |
1804 | ALKALOID METABOLIC PROCESS | 7 | -0.43 | -0.98 | 0.478 | 0.840 | 1.000 | 5651 | tags=71%, list=27%, signal=98% | |
1805 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE I PROMOTER | 11 | -0.41 | -0.98 | 0.475 | 0.841 | 1.000 | 4323 | tags=36%, list=21%, signal=46% | |
1806 | ARACHIDONIC ACID METABOLIC PROCESS | 42 | -0.30 | -0.98 | 0.468 | 0.842 | 1.000 | 3878 | tags=29%, list=19%, signal=35% | |
1807 | NEGATIVE REGULATION OF MYELOID CELL DIFFERENTIATION | 41 | -0.28 | -0.98 | 0.467 | 0.842 | 1.000 | 4047 | tags=27%, list=20%, signal=33% | |
1808 | COLUMNAR/CUBOIDAL EPITHELIAL CELL DIFFERENTIATION | 107 | -0.24 | -0.98 | 0.480 | 0.841 | 1.000 | 5823 | tags=37%, list=28%, signal=52% | |
1809 | AMEBOIDAL-TYPE CELL MIGRATION | 107 | -0.25 | -0.98 | 0.486 | 0.842 | 1.000 | 3677 | tags=24%, list=18%, signal=29% | |
1810 | POSITIVE REGULATION OF CELL PROJECTION ORGANIZATION | 188 | -0.22 | -0.98 | 0.487 | 0.841 | 1.000 | 4047 | tags=24%, list=20%, signal=30% | |
1811 | RESPONSE TO FATTY ACID | 23 | -0.34 | -0.98 | 0.477 | 0.842 | 1.000 | 3350 | tags=26%, list=16%, signal=31% | |
1812 | REGULATION OF MITOCHONDRIAL MEMBRANE PERMEABILITY INVOLVED IN APOPTOTIC PROCESS | 9 | -0.42 | -0.98 | 0.472 | 0.842 | 1.000 | 5433 | tags=56%, list=26%, signal=75% | |
1813 | PROTEIN INSERTION INTO MEMBRANE | 7 | -0.42 | -0.98 | 0.486 | 0.842 | 1.000 | 6206 | tags=57%, list=30%, signal=82% | |
1814 | SERINE FAMILY AMINO ACID METABOLIC PROCESS | 101 | -0.28 | -0.98 | 0.473 | 0.841 | 1.000 | 9861 | tags=60%, list=48%, signal=115% | |
1815 | WATER-SOLUBLE VITAMIN METABOLIC PROCESS | 84 | -0.24 | -0.98 | 0.480 | 0.841 | 1.000 | 5740 | tags=35%, list=28%, signal=48% | |
1816 | RESPONSE TO EPINEPHRINE | 9 | -0.41 | -0.98 | 0.488 | 0.841 | 1.000 | 160 | tags=11%, list=1%, signal=11% | |
1817 | CELLULAR RESPONSE TO EPINEPHRINE STIMULUS | 9 | -0.41 | -0.98 | 0.488 | 0.841 | 1.000 | 160 | tags=11%, list=1%, signal=11% | |
1818 | POSITIVE REGULATION OF LYMPHOCYTE MEDIATED IMMUNITY | 39 | -0.29 | -0.98 | 0.453 | 0.841 | 1.000 | 3350 | tags=21%, list=16%, signal=24% | |
1819 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE PHOSPHATASE SIGNALING PATHWAY | 5 | -0.46 | -0.98 | 0.497 | 0.841 | 1.000 | 4215 | tags=60%, list=20%, signal=75% | |
1820 | MONOAMINE TRANSPORT | 8 | -0.45 | -0.98 | 0.495 | 0.841 | 1.000 | 3114 | tags=25%, list=15%, signal=29% | |
1821 | MOTILE CILIUM ASSEMBLY | 9 | -0.41 | -0.98 | 0.481 | 0.840 | 1.000 | 7516 | tags=56%, list=36%, signal=87% | |
1822 | NEURAL NUCLEUS DEVELOPMENT | 63 | -0.24 | -0.98 | 0.501 | 0.840 | 1.000 | 2826 | tags=17%, list=14%, signal=20% | |
1823 | POSITIVE REGULATION OF MAPK CASCADE | 411 | -0.21 | -0.98 | 0.491 | 0.840 | 1.000 | 5650 | tags=29%, list=27%, signal=39% | |
1824 | SULFUR COMPOUND TRANSPORT | 22 | -0.32 | -0.98 | 0.471 | 0.840 | 1.000 | 3287 | tags=23%, list=16%, signal=27% | |
1825 | EMBRYONIC BODY MORPHOGENESIS | 10 | -0.37 | -0.98 | 0.494 | 0.839 | 1.000 | 6090 | tags=50%, list=30%, signal=71% | |
1826 | SYNCYTIUM FORMATION | 23 | -0.35 | -0.98 | 0.512 | 0.840 | 1.000 | 2372 | tags=26%, list=12%, signal=29% | |
1827 | CRANIAL SUTURE MORPHOGENESIS | 8 | -0.40 | -0.98 | 0.466 | 0.840 | 1.000 | 4206 | tags=38%, list=20%, signal=47% | |
1828 | NEURONAL ACTION POTENTIAL | 8 | -0.41 | -0.98 | 0.474 | 0.841 | 1.000 | 5039 | tags=38%, list=24%, signal=50% | |
1829 | SKELETAL MUSCLE CONTRACTION | 15 | -0.39 | -0.98 | 0.493 | 0.842 | 1.000 | 8336 | tags=73%, list=40%, signal=123% | |
1830 | REGULATION OF CELLULAR RESPONSE TO HYPOXIA | 5 | -0.44 | -0.98 | 0.513 | 0.842 | 1.000 | 3431 | tags=20%, list=17%, signal=24% | |
1831 | NEGATIVE REGULATION OF CELL CYCLE G2/M PHASE TRANSITION | 12 | -0.38 | -0.98 | 0.500 | 0.843 | 1.000 | 2678 | tags=25%, list=13%, signal=29% | |
1832 | HISTONE H4-K5 ACETYLATION | 6 | -0.47 | -0.98 | 0.516 | 0.843 | 1.000 | 8199 | tags=50%, list=40%, signal=83% | |
1833 | HISTONE H4-K8 ACETYLATION | 6 | -0.47 | -0.98 | 0.516 | 0.843 | 1.000 | 8199 | tags=50%, list=40%, signal=83% | |
1834 | POSITIVE REGULATION OF ACTIVATED T CELL PROLIFERATION | 16 | -0.34 | -0.98 | 0.499 | 0.843 | 1.000 | 7974 | tags=56%, list=39%, signal=92% | |
1835 | MYOBLAST FATE COMMITMENT | 5 | -0.49 | -0.98 | 0.510 | 0.843 | 1.000 | 7337 | tags=40%, list=36%, signal=62% | |
1836 | POSITIVE REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 50 | -0.29 | -0.98 | 0.476 | 0.843 | 1.000 | 6448 | tags=42%, list=31%, signal=61% | |
1837 | CELLULAR RESPONSE TO INTERLEUKIN-4 | 9 | -0.44 | -0.98 | 0.528 | 0.843 | 1.000 | 5743 | tags=33%, list=28%, signal=46% | |
1838 | HIGH-DENSITY LIPOPROTEIN PARTICLE ASSEMBLY | 6 | -0.47 | -0.98 | 0.480 | 0.843 | 1.000 | 5414 | tags=50%, list=26%, signal=68% | |
1839 | FUNGIFORM PAPILLA MORPHOGENESIS | 5 | -0.48 | -0.98 | 0.498 | 0.843 | 1.000 | 6442 | tags=60%, list=31%, signal=87% | |
1840 | REGULATION OF T CELL CYTOKINE PRODUCTION | 17 | -0.33 | -0.98 | 0.503 | 0.843 | 1.000 | 3350 | tags=29%, list=16%, signal=35% | |
1841 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 24 | -0.29 | -0.98 | 0.488 | 0.842 | 1.000 | 1120 | tags=17%, list=5%, signal=18% | |
1842 | POSITIVE REGULATION OF PROTEIN TARGETING TO MEMBRANE | 8 | -0.44 | -0.98 | 0.482 | 0.842 | 1.000 | 125 | tags=13%, list=1%, signal=13% | |
1843 | MELANOSOME LOCALIZATION | 15 | -0.30 | -0.98 | 0.478 | 0.844 | 1.000 | 5641 | tags=40%, list=27%, signal=55% | |
1844 | PIGMENT GRANULE LOCALIZATION | 15 | -0.30 | -0.98 | 0.478 | 0.844 | 1.000 | 5641 | tags=40%, list=27%, signal=55% | |
1845 | POSITIVE REGULATION OF CELL ADHESION | 228 | -0.22 | -0.97 | 0.507 | 0.844 | 1.000 | 5743 | tags=32%, list=28%, signal=44% | |
1846 | REGULATION OF METAL ION TRANSPORT | 178 | -0.22 | -0.97 | 0.500 | 0.845 | 1.000 | 5650 | tags=31%, list=27%, signal=42% | |
1847 | NEGATIVE REGULATION OF HEMATOPOIETIC PROGENITOR CELL DIFFERENTIATION | 8 | -0.42 | -0.97 | 0.485 | 0.847 | 1.000 | 8580 | tags=63%, list=42%, signal=107% | |
1848 | SULFATE TRANSMEMBRANE TRANSPORT | 7 | -0.41 | -0.97 | 0.509 | 0.847 | 1.000 | 80 | tags=14%, list=0%, signal=14% | |
1849 | DNA MODIFICATION | 65 | -0.25 | -0.97 | 0.492 | 0.846 | 1.000 | 6007 | tags=28%, list=29%, signal=39% | |
1850 | NEGATIVE REGULATION OF PROTEIN KINASE B SIGNALING | 21 | -0.30 | -0.97 | 0.482 | 0.847 | 1.000 | 5382 | tags=33%, list=26%, signal=45% | |
1851 | PROTEIN KINASE C-ACTIVATING G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 9 | -0.40 | -0.97 | 0.495 | 0.847 | 1.000 | 14 | tags=11%, list=0%, signal=11% | |
1852 | GASTRULATION WITH MOUTH FORMING SECOND | 28 | -0.29 | -0.97 | 0.512 | 0.847 | 1.000 | 4330 | tags=29%, list=21%, signal=36% | |
1853 | POSITIVE REGULATION OF ASTROCYTE DIFFERENTIATION | 10 | -0.41 | -0.97 | 0.509 | 0.847 | 1.000 | 4961 | tags=40%, list=24%, signal=53% | |
1854 | REGULATION OF STRIATED MUSCLE CELL APOPTOTIC PROCESS | 8 | -0.40 | -0.97 | 0.491 | 0.847 | 1.000 | 6988 | tags=50%, list=34%, signal=76% | |
1855 | RESPONSE TO INTERLEUKIN-4 | 10 | -0.42 | -0.97 | 0.506 | 0.848 | 1.000 | 5743 | tags=30%, list=28%, signal=42% | |
1856 | REGULATION OF GROWTH | 290 | -0.21 | -0.97 | 0.511 | 0.848 | 1.000 | 4932 | tags=25%, list=24%, signal=33% | |
1857 | AXON EXTENSION | 32 | -0.28 | -0.97 | 0.506 | 0.848 | 1.000 | 7038 | tags=41%, list=34%, signal=62% | |
1858 | TRANSMEMBRANE RECEPTOR PROTEIN SERINE/THREONINE KINASE SIGNALING PATHWAY | 155 | -0.22 | -0.97 | 0.482 | 0.848 | 1.000 | 5055 | tags=27%, list=25%, signal=36% | |
1859 | ALCOHOL CATABOLIC PROCESS | 21 | -0.32 | -0.97 | 0.495 | 0.848 | 1.000 | 4924 | tags=43%, list=24%, signal=56% | |
1860 | TELENCEPHALON DEVELOPMENT | 182 | -0.22 | -0.97 | 0.492 | 0.848 | 1.000 | 3729 | tags=20%, list=18%, signal=25% | |
1861 | REGULATION OF ANION TRANSPORT | 64 | -0.24 | -0.97 | 0.500 | 0.848 | 1.000 | 6270 | tags=31%, list=30%, signal=45% | |
1862 | CELL PROLIFERATION IN HINDBRAIN | 5 | -0.50 | -0.97 | 0.504 | 0.849 | 1.000 | 7449 | tags=60%, list=36%, signal=94% | |
1863 | CELL PROLIFERATION IN EXTERNAL GRANULE LAYER | 5 | -0.50 | -0.97 | 0.504 | 0.849 | 1.000 | 7449 | tags=60%, list=36%, signal=94% | |
1864 | CEREBELLAR GRANULE CELL PRECURSOR PROLIFERATION | 5 | -0.50 | -0.97 | 0.504 | 0.848 | 1.000 | 7449 | tags=60%, list=36%, signal=94% | |
1865 | NEGATIVE REGULATION OF NEURON MIGRATION | 10 | -0.40 | -0.97 | 0.486 | 0.848 | 1.000 | 3531 | tags=30%, list=17%, signal=36% | |
1866 | EMBRYONIC HINDLIMB MORPHOGENESIS | 29 | -0.29 | -0.97 | 0.490 | 0.848 | 1.000 | 7337 | tags=48%, list=36%, signal=75% | |
1867 | PEPTIDYL-GLUTAMIC ACID CARBOXYLATION | 13 | -0.37 | -0.97 | 0.517 | 0.848 | 1.000 | 2822 | tags=31%, list=14%, signal=36% | |
1868 | PROTEIN CARBOXYLATION | 13 | -0.37 | -0.97 | 0.517 | 0.847 | 1.000 | 2822 | tags=31%, list=14%, signal=36% | |
1869 | OVULATION FROM OVARIAN FOLLICLE | 7 | -0.40 | -0.97 | 0.524 | 0.847 | 1.000 | 3574 | tags=29%, list=17%, signal=35% | |
1870 | EMBRYONIC HEART TUBE LEFT/RIGHT PATTERN FORMATION | 5 | -0.46 | -0.97 | 0.510 | 0.846 | 1.000 | 427 | tags=20%, list=2%, signal=20% | |
1871 | DENDRITE DEVELOPMENT | 91 | -0.23 | -0.97 | 0.527 | 0.846 | 1.000 | 5312 | tags=32%, list=26%, signal=43% | |
1872 | NEGATIVE REGULATION OF LIPID TRANSPORT | 21 | -0.34 | -0.97 | 0.504 | 0.846 | 1.000 | 5990 | tags=52%, list=29%, signal=74% | |
1873 | VERY-LOW-DENSITY LIPOPROTEIN PARTICLE ASSEMBLY | 5 | -0.46 | -0.97 | 0.512 | 0.846 | 1.000 | 6398 | tags=60%, list=31%, signal=87% | |
1874 | CHONDROITIN SULFATE PROTEOGLYCAN METABOLIC PROCESS | 36 | -0.30 | -0.97 | 0.507 | 0.846 | 1.000 | 4434 | tags=33%, list=22%, signal=42% | |
1875 | NEGATIVE REGULATION OF POTASSIUM ION TRANSPORT | 17 | -0.32 | -0.97 | 0.502 | 0.846 | 1.000 | 4269 | tags=35%, list=21%, signal=44% | |
1876 | POSITIVE REGULATION OF ORGAN GROWTH | 13 | -0.38 | -0.97 | 0.516 | 0.845 | 1.000 | 1504 | tags=23%, list=7%, signal=25% | |
1877 | POSITIVE REGULATION OF HEART GROWTH | 13 | -0.38 | -0.97 | 0.516 | 0.845 | 1.000 | 1504 | tags=23%, list=7%, signal=25% | |
1878 | ENDOTHELIAL TUBE MORPHOGENESIS | 10 | -0.37 | -0.97 | 0.481 | 0.846 | 1.000 | 2879 | tags=20%, list=14%, signal=23% | |
1879 | HEMATOPOIETIC STEM CELL PROLIFERATION | 14 | -0.31 | -0.97 | 0.494 | 0.846 | 1.000 | 3431 | tags=36%, list=17%, signal=43% | |
1880 | LOCOMOTORY BEHAVIOR | 26 | -0.27 | -0.97 | 0.503 | 0.848 | 1.000 | 9578 | tags=69%, list=46%, signal=129% | |
1881 | CARDIAC ATRIUM MORPHOGENESIS | 27 | -0.29 | -0.97 | 0.496 | 0.848 | 1.000 | 4823 | tags=30%, list=23%, signal=39% | |
1882 | KINETOCHORE ORGANIZATION | 5 | -0.52 | -0.97 | 0.519 | 0.849 | 1.000 | 2478 | tags=40%, list=12%, signal=45% | |
1883 | NEGATIVE REGULATION OF ENDOTHELIAL CELL MIGRATION | 34 | -0.28 | -0.97 | 0.521 | 0.849 | 1.000 | 3312 | tags=21%, list=16%, signal=24% | |
1884 | PARAXIAL MESODERM FORMATION | 6 | -0.42 | -0.96 | 0.510 | 0.851 | 1.000 | 1192 | tags=17%, list=6%, signal=18% | |
1885 | NEGATIVE REGULATION OF CELL PROLIFERATION INVOLVED IN KIDNEY DEVELOPMENT | 5 | -0.47 | -0.96 | 0.520 | 0.851 | 1.000 | 4557 | tags=60%, list=22%, signal=77% | |
1886 | POSITIVE REGULATION OF STEM CELL PROLIFERATION | 32 | -0.28 | -0.96 | 0.504 | 0.851 | 1.000 | 3650 | tags=28%, list=18%, signal=34% | |
1887 | ENDOCARDIAL CUSHION TO MESENCHYMAL TRANSITION | 5 | -0.48 | -0.96 | 0.553 | 0.851 | 1.000 | 1084 | tags=20%, list=5%, signal=21% | |
1888 | NEGATIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE/THREONINE KINASE SIGNALING PATHWAY | 73 | -0.24 | -0.96 | 0.485 | 0.851 | 1.000 | 4940 | tags=27%, list=24%, signal=36% | |
1889 | DETECTION OF CHEMICAL STIMULUS | 57 | -0.29 | -0.96 | 0.535 | 0.851 | 1.000 | 7138 | tags=49%, list=35%, signal=75% | |
1890 | POSITIVE REGULATION OF REPRODUCTIVE PROCESS | 20 | -0.32 | -0.96 | 0.524 | 0.851 | 1.000 | 6111 | tags=50%, list=30%, signal=71% | |
1891 | ODONTOGENESIS OF DENTIN-CONTAINING TOOTH | 64 | -0.26 | -0.96 | 0.522 | 0.851 | 1.000 | 4506 | tags=30%, list=22%, signal=38% | |
1892 | CRANIAL SKELETAL SYSTEM DEVELOPMENT | 54 | -0.25 | -0.96 | 0.489 | 0.851 | 1.000 | 6656 | tags=41%, list=32%, signal=60% | |
1893 | PYRIMIDINE NUCLEOTIDE METABOLIC PROCESS | 17 | -0.38 | -0.96 | 0.507 | 0.851 | 1.000 | 2575 | tags=29%, list=12%, signal=34% | |
1894 | RESPONSE TO ATP | 14 | -0.35 | -0.96 | 0.529 | 0.851 | 1.000 | 4628 | tags=36%, list=22%, signal=46% | |
1895 | DENTATE GYRUS DEVELOPMENT | 16 | -0.32 | -0.96 | 0.494 | 0.851 | 1.000 | 377 | tags=13%, list=2%, signal=13% | |
1896 | REGULATION OF CALCIUM ION TRANSPORT | 109 | -0.24 | -0.96 | 0.523 | 0.851 | 1.000 | 5650 | tags=31%, list=27%, signal=43% | |
1897 | REGULATION OF ISOTYPE SWITCHING | 8 | -0.41 | -0.96 | 0.514 | 0.851 | 1.000 | 7124 | tags=63%, list=35%, signal=95% | |
1898 | NEGATIVE REGULATION OF CELL MOTILITY | 148 | -0.23 | -0.96 | 0.516 | 0.850 | 1.000 | 4566 | tags=27%, list=22%, signal=34% | |
1899 | REGULATION OF ANGIOGENESIS | 137 | -0.23 | -0.96 | 0.539 | 0.850 | 1.000 | 5173 | tags=28%, list=25%, signal=38% | |
1900 | SULFUR AMINO ACID TRANSPORT | 5 | -0.50 | -0.96 | 0.535 | 0.850 | 1.000 | 1864 | tags=20%, list=9%, signal=22% | |
1901 | CELLULAR RESPONSE TO RADIATION | 105 | -0.24 | -0.96 | 0.499 | 0.850 | 1.000 | 4833 | tags=27%, list=23%, signal=35% | |
1902 | HEART PROCESS | 51 | -0.27 | -0.96 | 0.512 | 0.850 | 1.000 | 4089 | tags=27%, list=20%, signal=34% | |
1903 | LIMBIC SYSTEM DEVELOPMENT | 73 | -0.24 | -0.96 | 0.558 | 0.851 | 1.000 | 5312 | tags=26%, list=26%, signal=35% | |
1904 | REGULATION OF INSULIN RECEPTOR SIGNALING PATHWAY | 17 | -0.33 | -0.96 | 0.522 | 0.851 | 1.000 | 2938 | tags=29%, list=14%, signal=34% | |
1905 | REGULATION OF RESPONSE TO FOOD | 12 | -0.36 | -0.96 | 0.508 | 0.850 | 1.000 | 6408 | tags=42%, list=31%, signal=60% | |
1906 | PROTEIN ACTIVATION CASCADE | 53 | -0.31 | -0.96 | 0.533 | 0.850 | 1.000 | 5376 | tags=38%, list=26%, signal=51% | |
1907 | REGULATION OF HUMORAL IMMUNE RESPONSE | 34 | -0.29 | -0.96 | 0.501 | 0.850 | 1.000 | 5376 | tags=41%, list=26%, signal=56% | |
1908 | VASCULAR SMOOTH MUSCLE CONTRACTION | 7 | -0.41 | -0.96 | 0.517 | 0.850 | 1.000 | 6719 | tags=57%, list=33%, signal=85% | |
1909 | REGULATION OF IMMUNOGLOBULIN PRODUCTION | 15 | -0.34 | -0.96 | 0.526 | 0.849 | 1.000 | 7124 | tags=47%, list=35%, signal=71% | |
1910 | NEGATIVE REGULATION OF CELL DEVELOPMENT | 211 | -0.22 | -0.96 | 0.527 | 0.849 | 1.000 | 5432 | tags=30%, list=26%, signal=40% | |
1911 | NEGATIVE REGULATION OF COMPLEMENT ACTIVATION | 8 | -0.43 | -0.96 | 0.521 | 0.849 | 1.000 | 5376 | tags=50%, list=26%, signal=68% | |
1912 | SEROTONIN RECEPTOR SIGNALING PATHWAY | 14 | -0.38 | -0.96 | 0.518 | 0.849 | 1.000 | 2295 | tags=21%, list=11%, signal=24% | |
1913 | POSITIVE REGULATION OF HOMOTYPIC CELL-CELL ADHESION | 136 | -0.23 | -0.96 | 0.551 | 0.849 | 1.000 | 5743 | tags=34%, list=28%, signal=47% | |
1914 | POSITIVE REGULATION OF LEUKOCYTE CELL-CELL ADHESION | 136 | -0.23 | -0.96 | 0.551 | 0.849 | 1.000 | 5743 | tags=34%, list=28%, signal=47% | |
1915 | RESPONSE TO AXON INJURY | 15 | -0.37 | -0.96 | 0.518 | 0.849 | 1.000 | 7812 | tags=53%, list=38%, signal=86% | |
1916 | RESPONSE TO RADIATION | 270 | -0.20 | -0.96 | 0.518 | 0.850 | 1.000 | 4897 | tags=26%, list=24%, signal=34% | |
1917 | NUCLEOTIDE PHOSPHORYLATION | 42 | -0.29 | -0.96 | 0.514 | 0.850 | 1.000 | 2064 | tags=14%, list=10%, signal=16% | |
1918 | NEGATIVE REGULATION OF ACTIN FILAMENT DEPOLYMERIZATION | 8 | -0.40 | -0.96 | 0.539 | 0.849 | 1.000 | 1697 | tags=25%, list=8%, signal=27% | |
1919 | REGULATION OF RAS PROTEIN SIGNAL TRANSDUCTION | 49 | -0.26 | -0.96 | 0.526 | 0.850 | 1.000 | 3815 | tags=29%, list=19%, signal=35% | |
1920 | NUCLEOSOME POSITIONING | 5 | -0.46 | -0.96 | 0.516 | 0.851 | 1.000 | 9021 | tags=80%, list=44%, signal=142% | |
1921 | NEGATIVE REGULATION OF MICROTUBULE POLYMERIZATION OR DEPOLYMERIZATION | 20 | -0.32 | -0.96 | 0.521 | 0.851 | 1.000 | 212 | tags=10%, list=1%, signal=10% | |
1922 | REGULATION OF OSTEOCLAST DIFFERENTIATION | 22 | -0.31 | -0.96 | 0.498 | 0.852 | 1.000 | 3092 | tags=18%, list=15%, signal=21% | |
1923 | BLOOD COAGULATION, INTRINSIC PATHWAY | 18 | -0.35 | -0.96 | 0.511 | 0.853 | 1.000 | 5152 | tags=39%, list=25%, signal=52% | |
1924 | ADULT HEART DEVELOPMENT | 16 | -0.32 | -0.96 | 0.519 | 0.853 | 1.000 | 7262 | tags=50%, list=35%, signal=77% | |
1925 | CELLULAR HORMONE METABOLIC PROCESS | 55 | -0.26 | -0.96 | 0.500 | 0.853 | 1.000 | 6598 | tags=38%, list=32%, signal=56% | |
1926 | COMPLEMENT ACTIVATION, CLASSICAL PATHWAY | 8 | -0.52 | -0.95 | 0.569 | 0.855 | 1.000 | 7717 | tags=63%, list=37%, signal=100% | |
1927 | REGULATION OF MESENCHYMAL CELL PROLIFERATION | 14 | -0.33 | -0.95 | 0.511 | 0.854 | 1.000 | 2803 | tags=29%, list=14%, signal=33% | |
1928 | DENDRITIC SPINE ORGANIZATION | 15 | -0.33 | -0.95 | 0.516 | 0.854 | 1.000 | 2298 | tags=20%, list=11%, signal=22% | |
1929 | MAMMARY GLAND EPITHELIAL CELL DIFFERENTIATION | 16 | -0.35 | -0.95 | 0.520 | 0.854 | 1.000 | 5555 | tags=38%, list=27%, signal=51% | |
1930 | LYMPHOCYTE MIGRATION | 18 | -0.34 | -0.95 | 0.536 | 0.853 | 1.000 | 794 | tags=17%, list=4%, signal=17% | |
1931 | RNA STABILIZATION | 23 | -0.28 | -0.95 | 0.514 | 0.854 | 1.000 | 577 | tags=9%, list=3%, signal=9% | |
1932 | NEURAL PLATE DEVELOPMENT | 9 | -0.44 | -0.95 | 0.518 | 0.854 | 1.000 | 5600 | tags=44%, list=27%, signal=61% | |
1933 | CARDIAC PACEMAKER CELL DIFFERENTIATION | 6 | -0.40 | -0.95 | 0.519 | 0.854 | 1.000 | 7484 | tags=67%, list=36%, signal=105% | |
1934 | OVULATION | 9 | -0.40 | -0.95 | 0.531 | 0.854 | 1.000 | 3961 | tags=33%, list=19%, signal=41% | |
1935 | ASYMMETRIC STEM CELL DIVISION | 7 | -0.45 | -0.95 | 0.537 | 0.855 | 1.000 | 2748 | tags=29%, list=13%, signal=33% | |
1936 | ARGININE METABOLIC PROCESS | 5 | -0.51 | -0.95 | 0.546 | 0.855 | 1.000 | 9149 | tags=40%, list=44%, signal=72% | |
1937 | ARGININE CATABOLIC PROCESS | 5 | -0.51 | -0.95 | 0.546 | 0.854 | 1.000 | 9149 | tags=40%, list=44%, signal=72% | |
1938 | COPPER ION TRANSPORT | 6 | -0.48 | -0.95 | 0.534 | 0.855 | 1.000 | 3647 | tags=33%, list=18%, signal=40% | |
1939 | NEGATIVE REGULATION OF T CELL DIFFERENTIATION | 19 | -0.30 | -0.95 | 0.530 | 0.855 | 1.000 | 3650 | tags=32%, list=18%, signal=38% | |
1940 | CARDIAC LEFT VENTRICLE MORPHOGENESIS | 12 | -0.37 | -0.95 | 0.535 | 0.855 | 1.000 | 4163 | tags=42%, list=20%, signal=52% | |
1941 | RESPIRATORY CHAIN COMPLEX IV ASSEMBLY | 6 | -0.45 | -0.95 | 0.538 | 0.855 | 1.000 | 74 | tags=17%, list=0%, signal=17% | |
1942 | NEGATIVE REGULATION OF MUSCLE CELL DIFFERENTIATION | 25 | -0.31 | -0.95 | 0.519 | 0.855 | 1.000 | 3961 | tags=28%, list=19%, signal=35% | |
1943 | NEGATIVE REGULATION OF T CELL MEDIATED IMMUNITY | 7 | -0.41 | -0.95 | 0.522 | 0.854 | 1.000 | 3278 | tags=29%, list=16%, signal=34% | |
1944 | POSITIVE REGULATION OF B CELL MEDIATED IMMUNITY | 9 | -0.40 | -0.95 | 0.530 | 0.855 | 1.000 | 4961 | tags=33%, list=24%, signal=44% | |
1945 | POSITIVE REGULATION OF IMMUNOGLOBULIN MEDIATED IMMUNE RESPONSE | 9 | -0.40 | -0.95 | 0.530 | 0.854 | 1.000 | 4961 | tags=33%, list=24%, signal=44% | |
1946 | IRON COORDINATION ENTITY TRANSPORT | 5 | -0.46 | -0.95 | 0.534 | 0.854 | 1.000 | 3473 | tags=40%, list=17%, signal=48% | |
1947 | REGULATION OF STEM CELL POPULATION MAINTENANCE | 9 | -0.36 | -0.95 | 0.537 | 0.854 | 1.000 | 8490 | tags=56%, list=41%, signal=94% | |
1948 | NITROGEN COMPOUND TRANSPORT | 249 | -0.20 | -0.95 | 0.545 | 0.854 | 1.000 | 3322 | tags=19%, list=16%, signal=22% | |
1949 | TETRAPYRROLE METABOLIC PROCESS | 40 | -0.28 | -0.95 | 0.510 | 0.854 | 1.000 | 2937 | tags=23%, list=14%, signal=26% | |
1950 | REGULATION OF INSULIN SECRETION | 105 | -0.21 | -0.95 | 0.539 | 0.854 | 1.000 | 6582 | tags=30%, list=32%, signal=43% | |
1951 | MATURE B CELL DIFFERENTIATION | 19 | -0.32 | -0.95 | 0.554 | 0.854 | 1.000 | 4047 | tags=26%, list=20%, signal=33% | |
1952 | NEGATIVE REGULATION OF CELL MIGRATION | 142 | -0.22 | -0.95 | 0.546 | 0.855 | 1.000 | 4566 | tags=27%, list=22%, signal=34% | |
1953 | PROSTAGLANDIN BIOSYNTHETIC PROCESS | 15 | -0.34 | -0.95 | 0.535 | 0.854 | 1.000 | 4874 | tags=33%, list=24%, signal=44% | |
1954 | PROSTANOID BIOSYNTHETIC PROCESS | 15 | -0.34 | -0.95 | 0.535 | 0.854 | 1.000 | 4874 | tags=33%, list=24%, signal=44% | |
1955 | CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 132 | -0.22 | -0.95 | 0.557 | 0.855 | 1.000 | 5313 | tags=27%, list=26%, signal=37% | |
1956 | BEHAVIOR | 124 | -0.23 | -0.95 | 0.543 | 0.856 | 1.000 | 7765 | tags=44%, list=38%, signal=71% | |
1957 | POSITIVE REGULATION OF CELL ACTIVATION | 181 | -0.22 | -0.95 | 0.564 | 0.856 | 1.000 | 5743 | tags=33%, list=28%, signal=46% | |
1958 | REGULATION OF STRIATED MUSCLE TISSUE DEVELOPMENT | 45 | -0.26 | -0.95 | 0.539 | 0.856 | 1.000 | 6442 | tags=38%, list=31%, signal=55% | |
1959 | VISUAL PERCEPTION | 76 | -0.26 | -0.95 | 0.523 | 0.856 | 1.000 | 6755 | tags=43%, list=33%, signal=64% | |
1960 | POSITIVE REGULATION OF BMP SIGNALING PATHWAY | 17 | -0.32 | -0.95 | 0.522 | 0.857 | 1.000 | 3245 | tags=29%, list=16%, signal=35% | |
1961 | POSITIVE REGULATION OF LEUKOCYTE ACTIVATION | 175 | -0.22 | -0.95 | 0.571 | 0.857 | 1.000 | 5743 | tags=33%, list=28%, signal=46% | |
1962 | POSITIVE REGULATION OF GROWTH | 129 | -0.21 | -0.95 | 0.548 | 0.857 | 1.000 | 5430 | tags=29%, list=26%, signal=39% | |
1963 | CELLULAR CALCIUM ION HOMEOSTASIS | 152 | -0.22 | -0.95 | 0.517 | 0.857 | 1.000 | 7820 | tags=48%, list=38%, signal=77% | |
1964 | NEGATIVE REGULATION OF SMOOTH MUSCLE CELL MIGRATION | 11 | -0.38 | -0.95 | 0.548 | 0.857 | 1.000 | 2138 | tags=27%, list=10%, signal=30% | |
1965 | VENTRICULAR SEPTUM DEVELOPMENT | 59 | -0.23 | -0.95 | 0.549 | 0.857 | 1.000 | 4823 | tags=27%, list=23%, signal=35% | |
1966 | MEGAKARYOCYTE DIFFERENTIATION | 17 | -0.33 | -0.95 | 0.503 | 0.858 | 1.000 | 1038 | tags=18%, list=5%, signal=19% | |
1967 | CELL-SUBSTRATE ADHERENS JUNCTION ASSEMBLY | 14 | -0.33 | -0.95 | 0.543 | 0.858 | 1.000 | 4566 | tags=43%, list=22%, signal=55% | |
1968 | FOCAL ADHESION ASSEMBLY | 14 | -0.33 | -0.95 | 0.543 | 0.858 | 1.000 | 4566 | tags=43%, list=22%, signal=55% | |
1969 | BLOOD VESSEL MORPHOGENESIS | 278 | -0.21 | -0.95 | 0.584 | 0.857 | 1.000 | 5311 | tags=29%, list=26%, signal=39% | |
1970 | NEGATIVE REGULATION OF VASCULATURE DEVELOPMENT | 58 | -0.27 | -0.95 | 0.537 | 0.857 | 1.000 | 3312 | tags=26%, list=16%, signal=31% | |
1971 | HEMATOPOIETIC PROGENITOR CELL DIFFERENTIATION | 104 | -0.23 | -0.95 | 0.565 | 0.857 | 1.000 | 5145 | tags=33%, list=25%, signal=43% | |
1972 | POSITIVE REGULATION OF CELL-CELL ADHESION | 152 | -0.22 | -0.95 | 0.573 | 0.857 | 1.000 | 5743 | tags=34%, list=28%, signal=46% | |
1973 | NEGATIVE REGULATION OF TUMOR NECROSIS FACTOR-MEDIATED SIGNALING PATHWAY | 10 | -0.39 | -0.95 | 0.516 | 0.856 | 1.000 | 1324 | tags=20%, list=6%, signal=21% | |
1974 | LENS FIBER CELL DEVELOPMENT | 15 | -0.35 | -0.95 | 0.517 | 0.856 | 1.000 | 6421 | tags=60%, list=31%, signal=87% | |
1975 | BONE MARROW DEVELOPMENT | 5 | -0.45 | -0.95 | 0.552 | 0.856 | 1.000 | 6922 | tags=40%, list=34%, signal=60% | |
1976 | CELLULAR AMINO ACID BIOSYNTHETIC PROCESS | 46 | -0.27 | -0.94 | 0.512 | 0.856 | 1.000 | 4328 | tags=28%, list=21%, signal=36% | |
1977 | MAINTENANCE OF ORGAN IDENTITY | 5 | -0.45 | -0.94 | 0.526 | 0.857 | 1.000 | 634 | tags=20%, list=3%, signal=21% | |
1978 | REGULATION OF T-HELPER 17 TYPE IMMUNE RESPONSE | 6 | -0.45 | -0.94 | 0.552 | 0.857 | 1.000 | 2493 | tags=33%, list=12%, signal=38% | |
1979 | PLATELET-DERIVED GROWTH FACTOR RECEPTOR-BETA SIGNALING PATHWAY | 7 | -0.42 | -0.94 | 0.540 | 0.857 | 1.000 | 5650 | tags=57%, list=27%, signal=79% | |
1980 | RETINAL METABOLIC PROCESS | 7 | -0.44 | -0.94 | 0.509 | 0.857 | 1.000 | 2655 | tags=29%, list=13%, signal=33% | |
1981 | POSITIVE REGULATION OF MITOCHONDRIAL CALCIUM ION CONCENTRATION | 5 | -0.46 | -0.94 | 0.532 | 0.860 | 1.000 | 8315 | tags=60%, list=40%, signal=101% | |
1982 | LYMPHANGIOGENESIS | 12 | -0.34 | -0.94 | 0.521 | 0.859 | 1.000 | 6736 | tags=50%, list=33%, signal=74% | |
1983 | NEGATIVE REGULATION OF B CELL ACTIVATION | 16 | -0.32 | -0.94 | 0.554 | 0.859 | 1.000 | 2543 | tags=25%, list=12%, signal=28% | |
1984 | NEGATIVE REGULATION OF PEPTIDYL-LYSINE ACETYLATION | 10 | -0.38 | -0.94 | 0.535 | 0.860 | 1.000 | 4940 | tags=30%, list=24%, signal=39% | |
1985 | REACTIVE NITROGEN SPECIES METABOLIC PROCESS | 25 | -0.29 | -0.94 | 0.527 | 0.860 | 1.000 | 4304 | tags=24%, list=21%, signal=30% | |
1986 | REGULATION OF LYMPHOCYTE ACTIVATION | 215 | -0.21 | -0.94 | 0.584 | 0.860 | 1.000 | 2803 | tags=18%, list=14%, signal=20% | |
1987 | INNER DYNEIN ARM ASSEMBLY | 8 | -0.41 | -0.94 | 0.550 | 0.860 | 1.000 | 9061 | tags=75%, list=44%, signal=134% | |
1988 | 2-OXOGLUTARATE METABOLIC PROCESS | 13 | -0.36 | -0.94 | 0.514 | 0.860 | 1.000 | 579 | tags=15%, list=3%, signal=16% | |
1989 | MULTICELLULAR ORGANISM REPRODUCTION | 344 | -0.19 | -0.94 | 0.608 | 0.859 | 1.000 | 5734 | tags=30%, list=28%, signal=41% | |
1990 | MUSCLE ORGAN MORPHOGENESIS | 67 | -0.26 | -0.94 | 0.516 | 0.859 | 1.000 | 4281 | tags=25%, list=21%, signal=32% | |
1991 | RESPONSE TO OXYGEN RADICAL | 8 | -0.42 | -0.94 | 0.547 | 0.859 | 1.000 | 8337 | tags=50%, list=40%, signal=84% | |
1992 | NEGATIVE REGULATION OF OSSIFICATION | 29 | -0.27 | -0.94 | 0.546 | 0.859 | 1.000 | 6504 | tags=41%, list=32%, signal=60% | |
1993 | FACE DEVELOPMENT | 51 | -0.23 | -0.94 | 0.573 | 0.860 | 1.000 | 590 | tags=10%, list=3%, signal=10% | |
1994 | POSITIVE REGULATION OF T CELL ACTIVATION | 133 | -0.23 | -0.94 | 0.593 | 0.861 | 1.000 | 5743 | tags=34%, list=28%, signal=47% | |
1995 | REGULATION OF RESPIRATORY SYSTEM PROCESS | 6 | -0.46 | -0.94 | 0.566 | 0.861 | 1.000 | 4392 | tags=33%, list=21%, signal=42% | |
1996 | METANEPHRIC GLOMERULUS VASCULATURE DEVELOPMENT | 6 | -0.45 | -0.94 | 0.528 | 0.860 | 1.000 | 7048 | tags=83%, list=34%, signal=127% | |
1997 | REGULATION OF PROTEIN LOCALIZATION TO CAJAL BODY | 8 | -0.49 | -0.94 | 0.554 | 0.861 | 1.000 | 3382 | tags=25%, list=16%, signal=30% | |
1998 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO CAJAL BODY | 8 | -0.49 | -0.94 | 0.554 | 0.861 | 1.000 | 3382 | tags=25%, list=16%, signal=30% | |
1999 | NEGATIVE REGULATION OF GROWTH | 137 | -0.23 | -0.94 | 0.542 | 0.861 | 1.000 | 4391 | tags=25%, list=21%, signal=31% | |
2000 | GLANDULAR EPITHELIAL CELL DEVELOPMENT | 17 | -0.31 | -0.94 | 0.538 | 0.862 | 1.000 | 4850 | tags=29%, list=24%, signal=38% | |
2001 | NEGATIVE REGULATION OF BLOOD VESSEL MORPHOGENESIS | 54 | -0.27 | -0.94 | 0.547 | 0.862 | 1.000 | 3312 | tags=26%, list=16%, signal=31% | |
2002 | VITAMIN D METABOLIC PROCESS | 10 | -0.35 | -0.94 | 0.526 | 0.863 | 1.000 | 6798 | tags=50%, list=33%, signal=75% | |
2003 | REGULATION OF TISSUE REMODELING | 22 | -0.32 | -0.94 | 0.541 | 0.863 | 1.000 | 790 | tags=14%, list=4%, signal=14% | |
2004 | AGING | 90 | -0.22 | -0.94 | 0.596 | 0.863 | 1.000 | 5419 | tags=29%, list=26%, signal=39% | |
2005 | NEGATIVE REGULATION OF CELLULAR CATABOLIC PROCESS | 108 | -0.23 | -0.94 | 0.571 | 0.863 | 1.000 | 3244 | tags=19%, list=16%, signal=23% | |
2006 | VASCULOGENESIS | 64 | -0.23 | -0.94 | 0.557 | 0.863 | 1.000 | 4163 | tags=27%, list=20%, signal=33% | |
2007 | NEGATIVE REGULATION OF OXIDATIVE STRESS-INDUCED NEURON DEATH | 8 | -0.35 | -0.94 | 0.534 | 0.864 | 1.000 | 4323 | tags=38%, list=21%, signal=47% | |
2008 | NEGATIVE REGULATION OF HISTONE ACETYLATION | 9 | -0.41 | -0.94 | 0.543 | 0.864 | 1.000 | 4940 | tags=33%, list=24%, signal=44% | |
2009 | REGULATION OF GLIAL CELL APOPTOTIC PROCESS | 7 | -0.41 | -0.93 | 0.562 | 0.865 | 1.000 | 140 | tags=14%, list=1%, signal=14% | |
2010 | NEGATIVE REGULATION OF GLIAL CELL APOPTOTIC PROCESS | 7 | -0.41 | -0.93 | 0.562 | 0.865 | 1.000 | 140 | tags=14%, list=1%, signal=14% | |
2011 | CARDIAC MUSCLE TISSUE GROWTH | 15 | -0.34 | -0.93 | 0.566 | 0.865 | 1.000 | 395 | tags=13%, list=2%, signal=14% | |
2012 | POSITIVE REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 18 | -0.32 | -0.93 | 0.517 | 0.865 | 1.000 | 6165 | tags=44%, list=30%, signal=63% | |
2013 | TRACHEA MORPHOGENESIS | 11 | -0.34 | -0.93 | 0.521 | 0.865 | 1.000 | 2803 | tags=27%, list=14%, signal=32% | |
2014 | AXIS SPECIFICATION | 76 | -0.23 | -0.93 | 0.581 | 0.865 | 1.000 | 5465 | tags=32%, list=27%, signal=43% | |
2015 | CALCIUM ION REGULATED EXOCYTOSIS | 20 | -0.32 | -0.93 | 0.565 | 0.865 | 1.000 | 7611 | tags=55%, list=37%, signal=87% | |
2016 | REGULATION OF LIPOPOLYSACCHARIDE-MEDIATED SIGNALING PATHWAY | 12 | -0.35 | -0.93 | 0.545 | 0.864 | 1.000 | 5157 | tags=33%, list=25%, signal=44% | |
2017 | GLOMERULAR MESANGIUM DEVELOPMENT | 7 | -0.44 | -0.93 | 0.558 | 0.864 | 1.000 | 5650 | tags=71%, list=27%, signal=98% | |
2018 | IRIS MORPHOGENESIS | 10 | -0.40 | -0.93 | 0.545 | 0.864 | 1.000 | 2252 | tags=20%, list=11%, signal=22% | |
2019 | HISTONE H4-K16 ACETYLATION | 5 | -0.47 | -0.93 | 0.559 | 0.864 | 1.000 | 8199 | tags=60%, list=40%, signal=100% | |
2020 | REGULATION OF LYMPHOCYTE MEDIATED IMMUNITY | 66 | -0.24 | -0.93 | 0.582 | 0.864 | 1.000 | 3840 | tags=21%, list=19%, signal=26% | |
2021 | REGULATION OF CELL ACTIVATION | 258 | -0.21 | -0.93 | 0.602 | 0.864 | 1.000 | 5743 | tags=32%, list=28%, signal=44% | |
2022 | POSITIVE REGULATION OF PRI-MIRNA TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 8 | -0.43 | -0.93 | 0.554 | 0.864 | 1.000 | 6421 | tags=50%, list=31%, signal=73% | |
2023 | CELL-SUBSTRATE ADHESION | 97 | -0.23 | -0.93 | 0.591 | 0.864 | 1.000 | 4886 | tags=31%, list=24%, signal=40% | |
2024 | REGULATION OF LIPID METABOLIC PROCESS | 158 | -0.21 | -0.93 | 0.606 | 0.864 | 1.000 | 5091 | tags=28%, list=25%, signal=37% | |
2025 | NEGATIVE REGULATION OF DENDRITIC SPINE MORPHOGENESIS | 5 | -0.45 | -0.93 | 0.539 | 0.865 | 1.000 | 1830 | tags=40%, list=9%, signal=44% | |
2026 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 76 | -0.25 | -0.93 | 0.552 | 0.866 | 1.000 | 3689 | tags=22%, list=18%, signal=27% | |
2027 | NEGATIVE REGULATION OF NEUROGENESIS | 180 | -0.21 | -0.93 | 0.563 | 0.866 | 1.000 | 5432 | tags=28%, list=26%, signal=38% | |
2028 | CLEAVAGE FURROW FORMATION | 5 | -0.42 | -0.93 | 0.571 | 0.866 | 1.000 | 3001 | tags=40%, list=15%, signal=47% | |
2029 | GLUCOCORTICOID METABOLIC PROCESS | 10 | -0.40 | -0.93 | 0.556 | 0.865 | 1.000 | 8732 | tags=80%, list=42%, signal=139% | |
2030 | NEGATIVE REGULATION OF CYCLIC NUCLEOTIDE BIOSYNTHETIC PROCESS | 22 | -0.31 | -0.93 | 0.544 | 0.866 | 1.000 | 5264 | tags=41%, list=26%, signal=55% | |
2031 | RENAL WATER HOMEOSTASIS | 33 | -0.26 | -0.93 | 0.581 | 0.866 | 1.000 | 4685 | tags=27%, list=23%, signal=35% | |
2032 | FEMALE GENITALIA DEVELOPMENT | 14 | -0.33 | -0.93 | 0.568 | 0.868 | 1.000 | 7595 | tags=57%, list=37%, signal=90% | |
2033 | EYE MORPHOGENESIS | 148 | -0.22 | -0.93 | 0.575 | 0.869 | 1.000 | 7002 | tags=42%, list=34%, signal=63% | |
2034 | NEGATIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 192 | -0.21 | -0.93 | 0.574 | 0.870 | 1.000 | 5432 | tags=28%, list=26%, signal=38% | |
2035 | PROTEIN HOMOOLIGOMERIZATION | 107 | -0.23 | -0.93 | 0.590 | 0.869 | 1.000 | 3560 | tags=22%, list=17%, signal=27% | |
2036 | REGULATION OF MALE GONAD DEVELOPMENT | 6 | -0.45 | -0.93 | 0.531 | 0.870 | 1.000 | 5050 | tags=67%, list=25%, signal=88% | |
2037 | CARDIAC CHAMBER MORPHOGENESIS | 105 | -0.23 | -0.93 | 0.559 | 0.870 | 1.000 | 4281 | tags=27%, list=21%, signal=33% | |
2038 | NEGATIVE REGULATION OF STRIATED MUSCLE TISSUE DEVELOPMENT | 17 | -0.34 | -0.93 | 0.563 | 0.870 | 1.000 | 6442 | tags=41%, list=31%, signal=60% | |
2039 | POSITIVE REGULATION OF EXOCYTOSIS | 51 | -0.24 | -0.93 | 0.566 | 0.870 | 1.000 | 3669 | tags=22%, list=18%, signal=26% | |
2040 | RESPONSE TO REDOX STATE | 8 | -0.39 | -0.93 | 0.544 | 0.870 | 1.000 | 2053 | tags=25%, list=10%, signal=28% | |
2041 | INTRINSIC APOPTOTIC SIGNALING PATHWAY BY P53 CLASS MEDIATOR | 26 | -0.32 | -0.93 | 0.550 | 0.870 | 1.000 | 5703 | tags=38%, list=28%, signal=53% | |
2042 | NEGATIVE REGULATION OF MUSCLE ORGAN DEVELOPMENT | 18 | -0.33 | -0.93 | 0.569 | 0.870 | 1.000 | 6442 | tags=39%, list=31%, signal=57% | |
2043 | REGULATION OF RESPONSE TO REACTIVE OXYGEN SPECIES | 20 | -0.30 | -0.93 | 0.574 | 0.870 | 1.000 | 3533 | tags=30%, list=17%, signal=36% | |
2044 | METANEPHRIC GLOMERULUS DEVELOPMENT | 9 | -0.40 | -0.93 | 0.538 | 0.869 | 1.000 | 3849 | tags=44%, list=19%, signal=55% | |
2045 | REGULATION OF ADRENERGIC RECEPTOR SIGNALING PATHWAY | 5 | -0.45 | -0.93 | 0.561 | 0.870 | 1.000 | 2622 | tags=20%, list=13%, signal=23% | |
2046 | REGULATION OF FATTY ACID METABOLIC PROCESS | 49 | -0.24 | -0.93 | 0.579 | 0.869 | 1.000 | 3690 | tags=29%, list=18%, signal=35% | |
2047 | CERAMIDE BIOSYNTHETIC PROCESS | 10 | -0.35 | -0.93 | 0.568 | 0.869 | 1.000 | 962 | tags=20%, list=5%, signal=21% | |
2048 | CEREBRAL CORTEX DEVELOPMENT | 92 | -0.22 | -0.93 | 0.611 | 0.869 | 1.000 | 3650 | tags=20%, list=18%, signal=24% | |
2049 | CARDIAC ATRIUM DEVELOPMENT | 32 | -0.26 | -0.93 | 0.558 | 0.868 | 1.000 | 4823 | tags=28%, list=23%, signal=37% | |
2050 | TACHYKININ RECEPTOR SIGNALING PATHWAY | 5 | -0.47 | -0.92 | 0.578 | 0.871 | 1.000 | 1681 | tags=20%, list=8%, signal=22% | |
2051 | NEGATIVE REGULATION OF NITRIC-OXIDE SYNTHASE ACTIVITY | 5 | -0.47 | -0.92 | 0.575 | 0.871 | 1.000 | 7138 | tags=60%, list=35%, signal=92% | |
2052 | NEGATIVE REGULATION OF PROTEIN KINASE ACTIVITY BY REGULATION OF PROTEIN PHOSPHORYLATION | 7 | -0.39 | -0.92 | 0.571 | 0.871 | 1.000 | 1278 | tags=29%, list=6%, signal=30% | |
2053 | FOREBRAIN DEVELOPMENT | 294 | -0.20 | -0.92 | 0.592 | 0.870 | 1.000 | 7466 | tags=39%, list=36%, signal=60% | |
2054 | FOREBRAIN NEURON DEVELOPMENT | 29 | -0.29 | -0.92 | 0.573 | 0.870 | 1.000 | 5559 | tags=34%, list=27%, signal=47% | |
2055 | NEGATIVE REGULATION OF ANGIOGENESIS | 52 | -0.26 | -0.92 | 0.570 | 0.870 | 1.000 | 3312 | tags=25%, list=16%, signal=30% | |
2056 | SUBSTANTIA NIGRA DEVELOPMENT | 44 | -0.25 | -0.92 | 0.630 | 0.870 | 1.000 | 1339 | tags=11%, list=6%, signal=12% | |
2057 | MUSCLE CELL FATE COMMITMENT | 14 | -0.33 | -0.92 | 0.549 | 0.870 | 1.000 | 6235 | tags=57%, list=30%, signal=82% | |
2058 | RESPONSE TO POTASSIUM ION | 5 | -0.41 | -0.92 | 0.542 | 0.870 | 1.000 | 7372 | tags=60%, list=36%, signal=93% | |
2059 | CELLULAR RESPONSE TO POTASSIUM ION | 5 | -0.41 | -0.92 | 0.542 | 0.870 | 1.000 | 7372 | tags=60%, list=36%, signal=93% | |
2060 | BLOOD VESSEL DEVELOPMENT | 365 | -0.20 | -0.92 | 0.648 | 0.869 | 1.000 | 6451 | tags=35%, list=31%, signal=49% | |
2061 | VITAMIN TRANSPORT | 16 | -0.32 | -0.92 | 0.543 | 0.869 | 1.000 | 3287 | tags=25%, list=16%, signal=30% | |
2062 | REGULATION OF PHOSPHATIDYLINOSITOL 3-KINASE SIGNALING | 54 | -0.24 | -0.92 | 0.595 | 0.869 | 1.000 | 7022 | tags=44%, list=34%, signal=67% | |
2063 | PHOSPHATIDYLGLYCEROL ACYL-CHAIN REMODELING | 15 | -0.33 | -0.92 | 0.547 | 0.869 | 1.000 | 1261 | tags=20%, list=6%, signal=21% | |
2064 | PROTEIN AUTOPROCESSING | 6 | -0.40 | -0.92 | 0.567 | 0.869 | 1.000 | 4352 | tags=50%, list=21%, signal=63% | |
2065 | MAMMARY GLAND DUCT MORPHOGENESIS | 37 | -0.27 | -0.92 | 0.557 | 0.868 | 1.000 | 5050 | tags=30%, list=25%, signal=39% | |
2066 | REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 157 | -0.21 | -0.92 | 0.621 | 0.868 | 1.000 | 3254 | tags=20%, list=16%, signal=24% | |
2067 | PHOTORECEPTOR CELL DEVELOPMENT | 43 | -0.24 | -0.92 | 0.617 | 0.869 | 1.000 | 5650 | tags=40%, list=27%, signal=54% | |
2068 | POSITIVE REGULATION OF LAMELLIPODIUM ASSEMBLY | 8 | -0.41 | -0.92 | 0.558 | 0.870 | 1.000 | 2689 | tags=25%, list=13%, signal=29% | |
2069 | EYE PHOTORECEPTOR CELL DIFFERENTIATION | 48 | -0.25 | -0.92 | 0.592 | 0.870 | 1.000 | 5650 | tags=40%, list=27%, signal=54% | |
2070 | REGULATION OF BASEMENT MEMBRANE ASSEMBLY INVOLVED IN EMBRYONIC BODY MORPHOGENESIS | 5 | -0.43 | -0.92 | 0.559 | 0.870 | 1.000 | 7353 | tags=60%, list=36%, signal=93% | |
2071 | POSITIVE REGULATION OF BASEMENT MEMBRANE ASSEMBLY INVOLVED IN EMBRYONIC BODY MORPHOGENESIS | 5 | -0.43 | -0.92 | 0.559 | 0.870 | 1.000 | 7353 | tags=60%, list=36%, signal=93% | |
2072 | NEGATIVE REGULATION OF RESPONSE TO FOOD | 7 | -0.42 | -0.92 | 0.563 | 0.869 | 1.000 | 9417 | tags=71%, list=46%, signal=132% | |
2073 | NEGATIVE REGULATION OF APPETITE | 7 | -0.42 | -0.92 | 0.563 | 0.869 | 1.000 | 9417 | tags=71%, list=46%, signal=132% | |
2074 | ALDITOL PHOSPHATE METABOLIC PROCESS | 23 | -0.30 | -0.92 | 0.571 | 0.869 | 1.000 | 3660 | tags=26%, list=18%, signal=32% | |
2075 | ANDROGEN BIOSYNTHETIC PROCESS | 8 | -0.41 | -0.92 | 0.545 | 0.868 | 1.000 | 5513 | tags=50%, list=27%, signal=68% | |
2076 | POSITIVE REGULATION OF T CELL DIFFERENTIATION | 33 | -0.26 | -0.92 | 0.617 | 0.868 | 1.000 | 5743 | tags=39%, list=28%, signal=55% | |
2077 | AXON CHOICE POINT RECOGNITION | 6 | -0.43 | -0.92 | 0.567 | 0.868 | 1.000 | 2062 | tags=33%, list=10%, signal=37% | |
2078 | PATTERN SPECIFICATION INVOLVED IN KIDNEY DEVELOPMENT | 5 | -0.46 | -0.92 | 0.580 | 0.868 | 1.000 | 1797 | tags=40%, list=9%, signal=44% | |
2079 | RENAL SYSTEM PATTERN SPECIFICATION | 5 | -0.46 | -0.92 | 0.580 | 0.867 | 1.000 | 1797 | tags=40%, list=9%, signal=44% | |
2080 | METANEPHRIC EPITHELIUM DEVELOPMENT | 14 | -0.36 | -0.92 | 0.562 | 0.867 | 1.000 | 5437 | tags=43%, list=26%, signal=58% | |
2081 | REGULATION OF MITOPHAGY | 29 | -0.29 | -0.92 | 0.541 | 0.868 | 1.000 | 4485 | tags=31%, list=22%, signal=40% | |
2082 | ACTIN FILAMENT-BASED MOVEMENT | 76 | -0.24 | -0.92 | 0.571 | 0.868 | 1.000 | 1002 | tags=11%, list=5%, signal=11% | |
2083 | NEUROMUSCULAR PROCESS | 25 | -0.31 | -0.92 | 0.550 | 0.868 | 1.000 | 7959 | tags=52%, list=39%, signal=85% | |
2084 | DENDRITIC SPINE MORPHOGENESIS | 12 | -0.35 | -0.92 | 0.584 | 0.867 | 1.000 | 2298 | tags=25%, list=11%, signal=28% | |
2085 | NEGATIVE REGULATION OF TRANSLATION IN RESPONSE TO STRESS | 9 | -0.40 | -0.92 | 0.535 | 0.867 | 1.000 | 4323 | tags=44%, list=21%, signal=56% | |
2086 | DEOXYRIBONUCLEOTIDE METABOLIC PROCESS | 21 | -0.36 | -0.92 | 0.562 | 0.868 | 1.000 | 2575 | tags=29%, list=12%, signal=33% | |
2087 | ASPARTATE FAMILY AMINO ACID METABOLIC PROCESS | 29 | -0.28 | -0.92 | 0.587 | 0.868 | 1.000 | 2832 | tags=21%, list=14%, signal=24% | |
2088 | SEQUESTERING OF EXTRACELLULAR LIGAND FROM RECEPTOR | 7 | -0.40 | -0.92 | 0.592 | 0.868 | 1.000 | 5856 | tags=57%, list=28%, signal=80% | |
2089 | MESONEPHRIC DUCT DEVELOPMENT | 7 | -0.40 | -0.92 | 0.568 | 0.868 | 1.000 | 7031 | tags=71%, list=34%, signal=108% | |
2090 | STEM CELL DIFFERENTIATION | 168 | -0.20 | -0.92 | 0.609 | 0.867 | 1.000 | 7048 | tags=40%, list=34%, signal=60% | |
2091 | POSITIVE REGULATION OF CELLULAR AMIDE METABOLIC PROCESS | 55 | -0.26 | -0.92 | 0.575 | 0.868 | 1.000 | 2140 | tags=16%, list=10%, signal=18% | |
2092 | CELLULAR RESPONSE TO GAMMA RADIATION | 8 | -0.40 | -0.92 | 0.599 | 0.868 | 1.000 | 2746 | tags=25%, list=13%, signal=29% | |
2093 | NEGATIVE REGULATION OF ENDOPLASMIC RETICULUM CALCIUM ION CONCENTRATION | 6 | -0.43 | -0.92 | 0.542 | 0.868 | 1.000 | 8315 | tags=50%, list=40%, signal=84% | |
2094 | POSITIVE REGULATION OF INSULIN RECEPTOR SIGNALING PATHWAY | 5 | -0.42 | -0.92 | 0.585 | 0.868 | 1.000 | 980 | tags=20%, list=5%, signal=21% | |
2095 | KERATINOCYTE DIFFERENTIATION | 59 | -0.23 | -0.92 | 0.606 | 0.868 | 1.000 | 3961 | tags=24%, list=19%, signal=29% | |
2096 | ANION HOMEOSTASIS | 30 | -0.28 | -0.92 | 0.574 | 0.868 | 1.000 | 2938 | tags=20%, list=14%, signal=23% | |
2097 | REGULATION OF VITAMIN METABOLIC PROCESS | 10 | -0.42 | -0.92 | 0.582 | 0.867 | 1.000 | 1184 | tags=20%, list=6%, signal=21% | |
2098 | REGULATION OF GENERATION OF PRECURSOR METABOLITES AND ENERGY | 46 | -0.26 | -0.92 | 0.574 | 0.868 | 1.000 | 4049 | tags=28%, list=20%, signal=35% | |
2099 | ETHANOLAMINE-CONTAINING COMPOUND METABOLIC PROCESS | 56 | -0.25 | -0.92 | 0.586 | 0.868 | 1.000 | 6630 | tags=41%, list=32%, signal=60% | |
2100 | SENSORY PERCEPTION OF MECHANICAL STIMULUS | 59 | -0.26 | -0.92 | 0.566 | 0.868 | 1.000 | 5992 | tags=36%, list=29%, signal=50% | |
2101 | REGULATION OF ACUTE INFLAMMATORY RESPONSE | 40 | -0.28 | -0.92 | 0.584 | 0.868 | 1.000 | 5376 | tags=38%, list=26%, signal=51% | |
2102 | POSITIVE REGULATION OF CELLULAR AMINE METABOLIC PROCESS | 9 | -0.35 | -0.92 | 0.602 | 0.868 | 1.000 | 4557 | tags=44%, list=22%, signal=57% | |
2103 | PEPTIDYL-GLUTAMIC ACID MODIFICATION | 22 | -0.30 | -0.92 | 0.590 | 0.869 | 1.000 | 2871 | tags=27%, list=14%, signal=32% | |
2104 | REGULATION OF CELLULAR RESPONSE TO OXIDATIVE STRESS | 38 | -0.24 | -0.92 | 0.602 | 0.869 | 1.000 | 4323 | tags=26%, list=21%, signal=33% | |
2105 | REGULATION OF RESPONSE TO OXIDATIVE STRESS | 39 | -0.24 | -0.91 | 0.593 | 0.869 | 1.000 | 4323 | tags=26%, list=21%, signal=32% | |
2106 | MULTICELLULAR ORGANISMAL REPRODUCTIVE PROCESS | 321 | -0.18 | -0.91 | 0.693 | 0.869 | 1.000 | 5734 | tags=29%, list=28%, signal=40% | |
2107 | PLATELET DEGRANULATION | 77 | -0.28 | -0.91 | 0.546 | 0.871 | 1.000 | 2447 | tags=21%, list=12%, signal=23% | |
2108 | EMBRYONIC DIGIT MORPHOGENESIS | 59 | -0.23 | -0.91 | 0.588 | 0.870 | 1.000 | 6710 | tags=39%, list=33%, signal=58% | |
2109 | RESPONSE TO NITRIC OXIDE | 10 | -0.35 | -0.91 | 0.556 | 0.870 | 1.000 | 5601 | tags=40%, list=27%, signal=55% | |
2110 | CHEMICAL SYNAPTIC TRANSMISSION, POSTSYNAPTIC | 39 | -0.28 | -0.91 | 0.573 | 0.871 | 1.000 | 6468 | tags=41%, list=31%, signal=60% | |
2111 | DIVALENT INORGANIC CATION HOMEOSTASIS | 172 | -0.20 | -0.91 | 0.595 | 0.871 | 1.000 | 7820 | tags=47%, list=38%, signal=75% | |
2112 | LUNG SECRETORY CELL DIFFERENTIATION | 11 | -0.35 | -0.91 | 0.586 | 0.870 | 1.000 | 4586 | tags=45%, list=22%, signal=58% | |
2113 | POSITIVE REGULATION OF RHO PROTEIN SIGNAL TRANSDUCTION | 9 | -0.39 | -0.91 | 0.571 | 0.870 | 1.000 | 444 | tags=22%, list=2%, signal=23% | |
2114 | HEPARAN SULFATE PROTEOGLYCAN BIOSYNTHETIC PROCESS | 7 | -0.40 | -0.91 | 0.591 | 0.870 | 1.000 | 3927 | tags=43%, list=19%, signal=53% | |
2115 | REGULATION OF PHAGOCYTOSIS, ENGULFMENT | 5 | -0.47 | -0.91 | 0.590 | 0.870 | 1.000 | 3512 | tags=60%, list=17%, signal=72% | |
2116 | ENDODERMAL CELL FATE COMMITMENT | 11 | -0.36 | -0.91 | 0.576 | 0.871 | 1.000 | 508 | tags=18%, list=2%, signal=19% | |
2117 | POSITIVE REGULATION OF CELL GROWTH | 98 | -0.20 | -0.91 | 0.654 | 0.871 | 1.000 | 4064 | tags=21%, list=20%, signal=27% | |
2118 | CALCIUM ION HOMEOSTASIS | 158 | -0.21 | -0.91 | 0.599 | 0.871 | 1.000 | 7820 | tags=48%, list=38%, signal=77% | |
2119 | ANGIOGENESIS | 189 | -0.21 | -0.91 | 0.624 | 0.870 | 1.000 | 6278 | tags=33%, list=30%, signal=47% | |
2120 | REGULATION OF VOLTAGE-GATED CALCIUM CHANNEL ACTIVITY | 11 | -0.36 | -0.91 | 0.576 | 0.870 | 1.000 | 8840 | tags=73%, list=43%, signal=127% | |
2121 | PHOSPHATIDYLGLYCEROL METABOLIC PROCESS | 28 | -0.30 | -0.91 | 0.554 | 0.870 | 1.000 | 2230 | tags=21%, list=11%, signal=24% | |
2122 | NEGATIVE REGULATION OF GLIOGENESIS | 24 | -0.30 | -0.91 | 0.565 | 0.870 | 1.000 | 3799 | tags=21%, list=18%, signal=26% | |
2123 | NEGATIVE REGULATION OF LOCOMOTION | 175 | -0.21 | -0.91 | 0.632 | 0.870 | 1.000 | 4566 | tags=27%, list=22%, signal=34% | |
2124 | CELLULAR RESPONSE TO INTERLEUKIN-1 | 33 | -0.27 | -0.91 | 0.590 | 0.871 | 1.000 | 3172 | tags=27%, list=15%, signal=32% | |
2125 | REVERSE CHOLESTEROL TRANSPORT | 11 | -0.37 | -0.91 | 0.564 | 0.871 | 1.000 | 1707 | tags=18%, list=8%, signal=20% | |
2126 | ASTROCYTE DEVELOPMENT | 20 | -0.28 | -0.91 | 0.596 | 0.872 | 1.000 | 5139 | tags=35%, list=25%, signal=47% | |
2127 | POSITIVE REGULATION OF CYCLIN-DEPENDENT PROTEIN SERINE/THREONINE KINASE ACTIVITY INVOLVED IN G1/S TRANSITION OF MITOTIC CELL CYCLE | 7 | -0.40 | -0.91 | 0.584 | 0.873 | 1.000 | 6924 | tags=57%, list=34%, signal=86% | |
2128 | CELLULAR RESPONSE TO ESTRADIOL STIMULUS | 13 | -0.32 | -0.91 | 0.560 | 0.873 | 1.000 | 837 | tags=15%, list=4%, signal=16% | |
2129 | URATE METABOLIC PROCESS | 9 | -0.41 | -0.91 | 0.560 | 0.873 | 1.000 | 8222 | tags=56%, list=40%, signal=92% | |
2130 | NEGATIVE REGULATION OF LIPASE ACTIVITY | 10 | -0.39 | -0.91 | 0.591 | 0.874 | 1.000 | 5414 | tags=50%, list=26%, signal=68% | |
2131 | POSITIVE REGULATION OF SECRETION | 174 | -0.20 | -0.91 | 0.656 | 0.874 | 1.000 | 2379 | tags=14%, list=12%, signal=15% | |
2132 | REGULATION OF NUCLEAR-TRANSCRIBED MRNA POLY(A) TAIL SHORTENING | 9 | -0.39 | -0.91 | 0.579 | 0.875 | 1.000 | 2757 | tags=22%, list=13%, signal=26% | |
2133 | POSITIVE REGULATION OF NUCLEAR-TRANSCRIBED MRNA POLY(A) TAIL SHORTENING | 9 | -0.39 | -0.91 | 0.579 | 0.874 | 1.000 | 2757 | tags=22%, list=13%, signal=26% | |
2134 | REGULATION OF HUMORAL IMMUNE RESPONSE MEDIATED BY CIRCULATING IMMUNOGLOBULIN | 5 | -0.46 | -0.91 | 0.605 | 0.874 | 1.000 | 7979 | tags=80%, list=39%, signal=131% | |
2135 | NEGATIVE REGULATION OF HUMORAL IMMUNE RESPONSE MEDIATED BY CIRCULATING IMMUNOGLOBULIN | 5 | -0.46 | -0.91 | 0.605 | 0.874 | 1.000 | 7979 | tags=80%, list=39%, signal=131% | |
2136 | PROTEIN LOCALIZATION TO SYNAPSE | 7 | -0.44 | -0.91 | 0.608 | 0.874 | 1.000 | 2298 | tags=29%, list=11%, signal=32% | |
2137 | OSTEOBLAST DIFFERENTIATION | 107 | -0.21 | -0.91 | 0.634 | 0.874 | 1.000 | 6504 | tags=34%, list=32%, signal=49% | |
2138 | GLYCOSAMINOGLYCAN METABOLIC PROCESS | 112 | -0.22 | -0.91 | 0.607 | 0.873 | 1.000 | 5484 | tags=31%, list=27%, signal=42% | |
2139 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION OF TASTE | 28 | -0.32 | -0.91 | 0.576 | 0.874 | 1.000 | 7095 | tags=50%, list=34%, signal=76% | |
2140 | GENE SILENCING BY MIRNA | 24 | -0.32 | -0.91 | 0.575 | 0.873 | 1.000 | 2757 | tags=25%, list=13%, signal=29% | |
2141 | ESTABLISHMENT OR MAINTENANCE OF CELL POLARITY | 68 | -0.23 | -0.91 | 0.622 | 0.873 | 1.000 | 4746 | tags=26%, list=23%, signal=34% | |
2142 | REGULATION OF MYELOID CELL DIFFERENTIATION | 83 | -0.23 | -0.91 | 0.625 | 0.873 | 1.000 | 4330 | tags=24%, list=21%, signal=30% | |
2143 | NEURAL TUBE PATTERNING | 34 | -0.27 | -0.91 | 0.604 | 0.873 | 1.000 | 6017 | tags=41%, list=29%, signal=58% | |
2144 | OOCYTE MATURATION | 10 | -0.37 | -0.91 | 0.601 | 0.873 | 1.000 | 5043 | tags=50%, list=24%, signal=66% | |
2145 | MIDBRAIN-HINDBRAIN BOUNDARY DEVELOPMENT | 7 | -0.45 | -0.91 | 0.586 | 0.873 | 1.000 | 6017 | tags=57%, list=29%, signal=81% | |
2146 | PARATHYROID GLAND DEVELOPMENT | 7 | -0.38 | -0.91 | 0.591 | 0.873 | 1.000 | 5943 | tags=43%, list=29%, signal=60% | |
2147 | REGULATION OF NEURONAL SYNAPTIC PLASTICITY | 16 | -0.35 | -0.91 | 0.577 | 0.873 | 1.000 | 6837 | tags=63%, list=33%, signal=93% | |
2148 | B CELL RECEPTOR SIGNALING PATHWAY | 21 | -0.30 | -0.91 | 0.622 | 0.873 | 1.000 | 935 | tags=14%, list=5%, signal=15% | |
2149 | REGULATION OF PEPTIDE TRANSPORT | 147 | -0.20 | -0.91 | 0.663 | 0.872 | 1.000 | 6031 | tags=27%, list=29%, signal=37% | |
2150 | REGULATION OF LEUKOCYTE CELL-CELL ADHESION | 179 | -0.21 | -0.91 | 0.644 | 0.872 | 1.000 | 5743 | tags=32%, list=28%, signal=44% | |
2151 | CELLULAR RESPONSE TO LIPID | 158 | -0.21 | -0.90 | 0.620 | 0.872 | 1.000 | 4115 | tags=24%, list=20%, signal=30% | |
2152 | ORGANELLE INHERITANCE | 8 | -0.39 | -0.90 | 0.578 | 0.873 | 1.000 | 3090 | tags=38%, list=15%, signal=44% | |
2153 | GOLGI INHERITANCE | 8 | -0.39 | -0.90 | 0.578 | 0.873 | 1.000 | 3090 | tags=38%, list=15%, signal=44% | |
2154 | AMINO-ACID BETAINE METABOLIC PROCESS | 10 | -0.35 | -0.90 | 0.570 | 0.873 | 1.000 | 6895 | tags=50%, list=33%, signal=75% | |
2155 | SOMATIC STEM CELL POPULATION MAINTENANCE | 66 | -0.24 | -0.90 | 0.613 | 0.872 | 1.000 | 3937 | tags=24%, list=19%, signal=30% | |
2156 | GLOMERULUS VASCULATURE DEVELOPMENT | 14 | -0.35 | -0.90 | 0.567 | 0.872 | 1.000 | 4259 | tags=50%, list=21%, signal=63% | |
2157 | REGULATION OF SEQUESTERING OF TRIGLYCERIDE | 9 | -0.37 | -0.90 | 0.569 | 0.871 | 1.000 | 2933 | tags=44%, list=14%, signal=52% | |
2158 | LEPTIN-MEDIATED SIGNALING PATHWAY | 8 | -0.39 | -0.90 | 0.619 | 0.872 | 1.000 | 4896 | tags=38%, list=24%, signal=49% | |
2159 | ARTERY MORPHOGENESIS | 50 | -0.26 | -0.90 | 0.605 | 0.872 | 1.000 | 6421 | tags=42%, list=31%, signal=61% | |
2160 | BASEMENT MEMBRANE ORGANIZATION | 7 | -0.41 | -0.90 | 0.584 | 0.872 | 1.000 | 3393 | tags=43%, list=16%, signal=51% | |
2161 | REGULATION OF CILIUM ASSEMBLY | 18 | -0.29 | -0.90 | 0.578 | 0.873 | 1.000 | 5411 | tags=33%, list=26%, signal=45% | |
2162 | RESPONSE TO IRON ION | 12 | -0.35 | -0.90 | 0.593 | 0.873 | 1.000 | 5056 | tags=42%, list=25%, signal=55% | |
2163 | REGULATION OF SYNAPTIC TRANSMISSION, GLUTAMATERGIC | 18 | -0.29 | -0.90 | 0.604 | 0.874 | 1.000 | 6395 | tags=50%, list=31%, signal=72% | |
2164 | REGULATION OF BICELLULAR TIGHT JUNCTION ASSEMBLY | 10 | -0.35 | -0.90 | 0.579 | 0.873 | 1.000 | 140 | tags=10%, list=1%, signal=10% | |
2165 | REGULATION OF INFLAMMATORY RESPONSE | 122 | -0.23 | -0.90 | 0.607 | 0.873 | 1.000 | 4905 | tags=29%, list=24%, signal=37% | |
2166 | REGULATION OF CELL-CELL ADHESION | 231 | -0.20 | -0.90 | 0.673 | 0.873 | 1.000 | 5743 | tags=31%, list=28%, signal=42% | |
2167 | ORGANIC ACID BIOSYNTHETIC PROCESS | 136 | -0.22 | -0.90 | 0.628 | 0.873 | 1.000 | 3910 | tags=23%, list=19%, signal=28% | |
2168 | CARBOXYLIC ACID BIOSYNTHETIC PROCESS | 136 | -0.22 | -0.90 | 0.628 | 0.873 | 1.000 | 3910 | tags=23%, list=19%, signal=28% | |
2169 | POSITIVE REGULATION OF T CELL PROLIFERATION | 52 | -0.24 | -0.90 | 0.612 | 0.872 | 1.000 | 3350 | tags=21%, list=16%, signal=25% | |
2170 | OTIC VESICLE MORPHOGENESIS | 11 | -0.35 | -0.90 | 0.575 | 0.872 | 1.000 | 4823 | tags=45%, list=23%, signal=59% | |
2171 | SENSORY PERCEPTION OF SOUND | 57 | -0.26 | -0.90 | 0.579 | 0.872 | 1.000 | 5992 | tags=35%, list=29%, signal=49% | |
2172 | LABYRINTHINE LAYER BLOOD VESSEL DEVELOPMENT | 20 | -0.31 | -0.90 | 0.581 | 0.873 | 1.000 | 8456 | tags=60%, list=41%, signal=102% | |
2173 | ENDOPLASMIC RETICULUM UNFOLDED PROTEIN RESPONSE | 85 | -0.26 | -0.90 | 0.574 | 0.873 | 1.000 | 3344 | tags=22%, list=16%, signal=27% | |
2174 | REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 39 | -0.25 | -0.90 | 0.606 | 0.875 | 1.000 | 3878 | tags=26%, list=19%, signal=32% | |
2175 | NEGATIVE REGULATION OF IMMUNE RESPONSE | 62 | -0.25 | -0.90 | 0.587 | 0.875 | 1.000 | 4372 | tags=29%, list=21%, signal=37% | |
2176 | REGULATION OF BLOOD COAGULATION | 55 | -0.26 | -0.90 | 0.606 | 0.875 | 1.000 | 6128 | tags=40%, list=30%, signal=57% | |
2177 | REGULATION OF HEMOSTASIS | 55 | -0.26 | -0.90 | 0.606 | 0.874 | 1.000 | 6128 | tags=40%, list=30%, signal=57% | |
2178 | ORGANIC ACID TRANSMEMBRANE TRANSPORT | 72 | -0.25 | -0.90 | 0.635 | 0.874 | 1.000 | 1864 | tags=17%, list=9%, signal=18% | |
2179 | REGULATION OF STEROL TRANSPORT | 28 | -0.30 | -0.90 | 0.605 | 0.874 | 1.000 | 5946 | tags=43%, list=29%, signal=60% | |
2180 | REGULATION OF CHOLESTEROL TRANSPORT | 28 | -0.30 | -0.90 | 0.605 | 0.873 | 1.000 | 5946 | tags=43%, list=29%, signal=60% | |
2181 | CELLULAR DIVALENT INORGANIC CATION HOMEOSTASIS | 161 | -0.20 | -0.90 | 0.634 | 0.875 | 1.000 | 7820 | tags=47%, list=38%, signal=74% | |
2182 | POSITIVE REGULATION OF SECRETION BY CELL | 159 | -0.20 | -0.90 | 0.676 | 0.874 | 1.000 | 3669 | tags=19%, list=18%, signal=23% | |
2183 | LIPOXIN METABOLIC PROCESS | 6 | -0.44 | -0.90 | 0.598 | 0.874 | 1.000 | 683 | tags=17%, list=3%, signal=17% | |
2184 | PHOSPHATIDYLETHANOLAMINE ACYL-CHAIN REMODELING | 19 | -0.31 | -0.90 | 0.588 | 0.875 | 1.000 | 2230 | tags=21%, list=11%, signal=24% | |
2185 | REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 25 | -0.27 | -0.90 | 0.652 | 0.876 | 1.000 | 2938 | tags=24%, list=14%, signal=28% | |
2186 | NEGATIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 54 | -0.25 | -0.90 | 0.614 | 0.876 | 1.000 | 4940 | tags=28%, list=24%, signal=36% | |
2187 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 54 | -0.25 | -0.90 | 0.614 | 0.876 | 1.000 | 4940 | tags=28%, list=24%, signal=36% | |
2188 | CARDIAC VENTRICLE MORPHOGENESIS | 60 | -0.24 | -0.90 | 0.625 | 0.875 | 1.000 | 4823 | tags=30%, list=23%, signal=39% | |
2189 | QUINONE METABOLIC PROCESS | 23 | -0.31 | -0.90 | 0.585 | 0.875 | 1.000 | 3414 | tags=26%, list=17%, signal=31% | |
2190 | VENTRICULAR CARDIAC MUSCLE TISSUE DEVELOPMENT | 45 | -0.26 | -0.90 | 0.597 | 0.875 | 1.000 | 6235 | tags=36%, list=30%, signal=51% | |
2191 | NEGATIVE REGULATION OF TRANSLATIONAL INITIATION IN RESPONSE TO STRESS | 7 | -0.44 | -0.90 | 0.593 | 0.875 | 1.000 | 4323 | tags=43%, list=21%, signal=54% | |
2192 | NEUROLOGICAL SYSTEM PROCESS | 293 | -0.22 | -0.90 | 0.617 | 0.874 | 1.000 | 6687 | tags=37%, list=32%, signal=54% | |
2193 | POSITIVE REGULATION OF MEMBRANE DEPOLARIZATION | 6 | -0.40 | -0.90 | 0.617 | 0.874 | 1.000 | 4820 | tags=33%, list=23%, signal=43% | |
2194 | POSITIVE REGULATION OF NEUTROPHIL CHEMOTAXIS | 13 | -0.33 | -0.90 | 0.625 | 0.874 | 1.000 | 794 | tags=15%, list=4%, signal=16% | |
2195 | POSITIVE REGULATION OF RUFFLE ASSEMBLY | 6 | -0.45 | -0.90 | 0.613 | 0.874 | 1.000 | 7967 | tags=83%, list=39%, signal=136% | |
2196 | ALPHA-AMINO ACID BIOSYNTHETIC PROCESS | 34 | -0.28 | -0.90 | 0.602 | 0.874 | 1.000 | 3910 | tags=29%, list=19%, signal=36% | |
2197 | HEME BIOSYNTHETIC PROCESS | 15 | -0.33 | -0.90 | 0.597 | 0.875 | 1.000 | 1215 | tags=13%, list=6%, signal=14% | |
2198 | LYMPH VESSEL DEVELOPMENT | 20 | -0.28 | -0.90 | 0.615 | 0.875 | 1.000 | 7768 | tags=50%, list=38%, signal=80% | |
2199 | NEGATIVE REGULATION OF ACTIN FILAMENT BUNDLE ASSEMBLY | 13 | -0.32 | -0.89 | 0.611 | 0.876 | 1.000 | 2298 | tags=31%, list=11%, signal=35% | |
2200 | REGULATION OF NEURON DEATH | 96 | -0.20 | -0.89 | 0.664 | 0.876 | 1.000 | 4384 | tags=22%, list=21%, signal=28% | |
2201 | POSITIVE REGULATION OF DELAYED RECTIFIER POTASSIUM CHANNEL ACTIVITY | 5 | -0.44 | -0.89 | 0.588 | 0.875 | 1.000 | 5264 | tags=60%, list=26%, signal=81% | |
2202 | POSITIVE REGULATION OF VOLTAGE-GATED POTASSIUM CHANNEL ACTIVITY | 5 | -0.44 | -0.89 | 0.588 | 0.875 | 1.000 | 5264 | tags=60%, list=26%, signal=81% | |
2203 | REGULATION OF MACROPHAGE DERIVED FOAM CELL DIFFERENTIATION | 20 | -0.29 | -0.89 | 0.589 | 0.876 | 1.000 | 2933 | tags=20%, list=14%, signal=23% | |
2204 | HAIR CELL DIFFERENTIATION | 35 | -0.25 | -0.89 | 0.631 | 0.876 | 1.000 | 6073 | tags=40%, list=29%, signal=57% | |
2205 | DEMETHYLATION | 25 | -0.26 | -0.89 | 0.620 | 0.876 | 1.000 | 5651 | tags=36%, list=27%, signal=50% | |
2206 | POSITIVE REGULATION OF ACTIN FILAMENT DEPOLYMERIZATION | 8 | -0.36 | -0.89 | 0.608 | 0.876 | 1.000 | 2689 | tags=25%, list=13%, signal=29% | |
2207 | REGULATION OF MUSCLE CONTRACTION | 82 | -0.24 | -0.89 | 0.596 | 0.877 | 1.000 | 5327 | tags=35%, list=26%, signal=48% | |
2208 | CORPUS CALLOSUM DEVELOPMENT | 9 | -0.34 | -0.89 | 0.578 | 0.877 | 1.000 | 75 | tags=11%, list=0%, signal=11% | |
2209 | HORMONE BIOSYNTHETIC PROCESS | 29 | -0.30 | -0.89 | 0.579 | 0.876 | 1.000 | 8058 | tags=55%, list=39%, signal=90% | |
2210 | NEGATIVE REGULATION OF CHEMOTAXIS | 27 | -0.27 | -0.89 | 0.636 | 0.876 | 1.000 | 2062 | tags=19%, list=10%, signal=21% | |
2211 | REGULATION OF RECEPTOR BIOSYNTHETIC PROCESS | 14 | -0.33 | -0.89 | 0.596 | 0.876 | 1.000 | 2933 | tags=29%, list=14%, signal=33% | |
2212 | ACUTE INFLAMMATORY RESPONSE | 20 | -0.30 | -0.89 | 0.642 | 0.877 | 1.000 | 3350 | tags=30%, list=16%, signal=36% | |
2213 | REGULATION OF PROTEIN EXPORT FROM NUCLEUS | 18 | -0.31 | -0.89 | 0.620 | 0.877 | 1.000 | 4626 | tags=28%, list=22%, signal=36% | |
2214 | MYELOID LEUKOCYTE MIGRATION | 44 | -0.25 | -0.89 | 0.639 | 0.878 | 1.000 | 6876 | tags=34%, list=33%, signal=51% | |
2215 | POSITIVE REGULATION OF LIPID METABOLIC PROCESS | 80 | -0.23 | -0.89 | 0.653 | 0.881 | 1.000 | 5743 | tags=33%, list=28%, signal=45% | |
2216 | MUSCLE CELL PROLIFERATION | 14 | -0.34 | -0.89 | 0.622 | 0.883 | 1.000 | 395 | tags=14%, list=2%, signal=15% | |
2217 | POSITIVE REGULATION OF PEPTIDYL-SERINE PHOSPHORYLATION | 48 | -0.24 | -0.89 | 0.676 | 0.883 | 1.000 | 3951 | tags=25%, list=19%, signal=31% | |
2218 | PLASMINOGEN ACTIVATION | 7 | -0.43 | -0.89 | 0.602 | 0.883 | 1.000 | 5261 | tags=43%, list=26%, signal=58% | |
2219 | REGULATION OF LIPID TRANSPORT | 55 | -0.25 | -0.89 | 0.614 | 0.883 | 1.000 | 6961 | tags=42%, list=34%, signal=63% | |
2220 | POSITIVE REGULATION OF ION TRANSPORT | 118 | -0.22 | -0.89 | 0.648 | 0.883 | 1.000 | 5650 | tags=30%, list=27%, signal=41% | |
2221 | REGULATION OF RESPONSE TO WOUNDING | 208 | -0.21 | -0.89 | 0.642 | 0.882 | 1.000 | 5650 | tags=32%, list=27%, signal=44% | |
2222 | NEGATIVE REGULATION OF NEURON DIFFERENTIATION | 141 | -0.21 | -0.89 | 0.668 | 0.882 | 1.000 | 7038 | tags=38%, list=34%, signal=58% | |
2223 | AUDITORY RECEPTOR CELL DIFFERENTIATION | 30 | -0.26 | -0.89 | 0.606 | 0.883 | 1.000 | 6073 | tags=43%, list=29%, signal=61% | |
2224 | CELLULAR RESPONSE TO UNFOLDED PROTEIN | 88 | -0.25 | -0.89 | 0.602 | 0.883 | 1.000 | 3344 | tags=22%, list=16%, signal=26% | |
2225 | CREATINE METABOLIC PROCESS | 10 | -0.33 | -0.89 | 0.634 | 0.883 | 1.000 | 4902 | tags=30%, list=24%, signal=39% | |
2226 | STEROID HORMONE MEDIATED SIGNALING PATHWAY | 13 | -0.32 | -0.89 | 0.604 | 0.883 | 1.000 | 4914 | tags=38%, list=24%, signal=50% | |
2227 | REGULATION OF MESODERM DEVELOPMENT | 7 | -0.38 | -0.89 | 0.598 | 0.883 | 1.000 | 4745 | tags=43%, list=23%, signal=56% | |
2228 | POSITIVE REGULATION OF TRANSLATION | 44 | -0.27 | -0.89 | 0.610 | 0.882 | 1.000 | 1304 | tags=14%, list=6%, signal=15% | |
2229 | CENTRIOLE-CENTRIOLE COHESION | 5 | -0.44 | -0.89 | 0.625 | 0.882 | 1.000 | 158 | tags=20%, list=1%, signal=20% | |
2230 | GLIAL CELL PROLIFERATION | 5 | -0.43 | -0.89 | 0.620 | 0.882 | 1.000 | 8151 | tags=60%, list=40%, signal=99% | |
2231 | CARDIOLIPIN METABOLIC PROCESS | 10 | -0.36 | -0.89 | 0.594 | 0.881 | 1.000 | 2230 | tags=30%, list=11%, signal=34% | |
2232 | POSITIVE REGULATION OF MESENCHYMAL CELL PROLIFERATION | 10 | -0.33 | -0.89 | 0.617 | 0.882 | 1.000 | 2803 | tags=30%, list=14%, signal=35% | |
2233 | REGULATION OF T CELL ACTIVATION | 171 | -0.21 | -0.89 | 0.706 | 0.882 | 1.000 | 5743 | tags=32%, list=28%, signal=44% | |
2234 | MULTICELLULAR ORGANISM GROWTH | 80 | -0.21 | -0.89 | 0.691 | 0.882 | 1.000 | 2465 | tags=16%, list=12%, signal=18% | |
2235 | NEGATIVE REGULATION OF DENDRITIC SPINE DEVELOPMENT | 7 | -0.39 | -0.88 | 0.594 | 0.883 | 1.000 | 5815 | tags=57%, list=28%, signal=80% | |
2236 | REGULATION OF LEUKOCYTE ACTIVATION | 237 | -0.20 | -0.88 | 0.713 | 0.884 | 1.000 | 5515 | tags=30%, list=27%, signal=40% | |
2237 | LABYRINTHINE LAYER MORPHOGENESIS | 24 | -0.28 | -0.88 | 0.625 | 0.884 | 1.000 | 2211 | tags=17%, list=11%, signal=19% | |
2238 | POSITIVE REGULATION OF IMMUNE EFFECTOR PROCESS | 87 | -0.22 | -0.88 | 0.663 | 0.884 | 1.000 | 5743 | tags=31%, list=28%, signal=43% | |
2239 | POSITIVE REGULATION OF TRANSMEMBRANE TRANSPORT | 73 | -0.23 | -0.88 | 0.640 | 0.884 | 1.000 | 6568 | tags=37%, list=32%, signal=54% | |
2240 | POSITIVE REGULATION OF T-HELPER 17 TYPE IMMUNE RESPONSE | 5 | -0.46 | -0.88 | 0.613 | 0.884 | 1.000 | 239 | tags=20%, list=1%, signal=20% | |
2241 | POSITIVE REGULATION OF LOCOMOTION | 260 | -0.20 | -0.88 | 0.701 | 0.885 | 1.000 | 3293 | tags=18%, list=16%, signal=22% | |
2242 | EPITHELIUM MIGRATION | 55 | -0.26 | -0.88 | 0.649 | 0.884 | 1.000 | 2211 | tags=18%, list=11%, signal=20% | |
2243 | NEURAL PRECURSOR CELL PROLIFERATION | 62 | -0.23 | -0.88 | 0.673 | 0.884 | 1.000 | 5688 | tags=34%, list=28%, signal=47% | |
2244 | REGULATION OF SECRETION | 353 | -0.19 | -0.88 | 0.681 | 0.887 | 1.000 | 3824 | tags=19%, list=19%, signal=23% | |
2245 | PURINE NUCLEOTIDE TRANSPORT | 5 | -0.43 | -0.88 | 0.635 | 0.886 | 1.000 | 4393 | tags=40%, list=21%, signal=51% | |
2246 | REGULATION OF CELLULAR RESPIRATION | 9 | -0.37 | -0.88 | 0.629 | 0.886 | 1.000 | 3937 | tags=33%, list=19%, signal=41% | |
2247 | REGULATION OF HISTONE H3-K27 METHYLATION | 6 | -0.40 | -0.88 | 0.607 | 0.886 | 1.000 | 4918 | tags=50%, list=24%, signal=66% | |
2248 | POSITIVE REGULATION OF REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 24 | -0.30 | -0.88 | 0.623 | 0.886 | 1.000 | 4304 | tags=29%, list=21%, signal=37% | |
2249 | CARDIAC VENTRICLE DEVELOPMENT | 108 | -0.20 | -0.88 | 0.686 | 0.887 | 1.000 | 4823 | tags=27%, list=23%, signal=35% | |
2250 | REGULATION OF COAGULATION | 57 | -0.25 | -0.88 | 0.647 | 0.887 | 1.000 | 7097 | tags=46%, list=34%, signal=69% | |
2251 | SYNAPTIC VESICLE EXOCYTOSIS | 14 | -0.33 | -0.88 | 0.603 | 0.887 | 1.000 | 3091 | tags=29%, list=15%, signal=34% | |
2252 | REGULATION OF DENDRITIC CELL DIFFERENTIATION | 6 | -0.44 | -0.88 | 0.617 | 0.887 | 1.000 | 1800 | tags=17%, list=9%, signal=18% | |
2253 | POSITIVE REGULATION OF AMINE TRANSPORT | 9 | -0.36 | -0.88 | 0.605 | 0.887 | 1.000 | 6408 | tags=44%, list=31%, signal=64% | |
2254 | MUSCLE TISSUE MORPHOGENESIS | 60 | -0.24 | -0.88 | 0.623 | 0.889 | 1.000 | 4281 | tags=25%, list=21%, signal=31% | |
2255 | NON-CANONICAL WNT SIGNALING PATHWAY | 23 | -0.27 | -0.88 | 0.642 | 0.888 | 1.000 | 6710 | tags=48%, list=33%, signal=71% | |
2256 | POSITIVE REGULATION OF MAP KINASE ACTIVITY | 130 | -0.21 | -0.88 | 0.645 | 0.888 | 1.000 | 5650 | tags=30%, list=27%, signal=41% | |
2257 | REGULATION OF LIPID CATABOLIC PROCESS | 33 | -0.26 | -0.88 | 0.653 | 0.888 | 1.000 | 4193 | tags=27%, list=20%, signal=34% | |
2258 | VAGINA DEVELOPMENT | 10 | -0.35 | -0.88 | 0.611 | 0.888 | 1.000 | 1014 | tags=20%, list=5%, signal=21% | |
2259 | REGULATION OF OXIDATIVE STRESS-INDUCED CELL DEATH | 32 | -0.23 | -0.88 | 0.661 | 0.888 | 1.000 | 4323 | tags=28%, list=21%, signal=36% | |
2260 | POSITIVE REGULATION OF CGMP METABOLIC PROCESS | 9 | -0.38 | -0.88 | 0.598 | 0.888 | 1.000 | 6848 | tags=67%, list=33%, signal=100% | |
2261 | ACTIVIN RECEPTOR SIGNALING PATHWAY | 17 | -0.30 | -0.88 | 0.611 | 0.887 | 1.000 | 4330 | tags=41%, list=21%, signal=52% | |
2262 | REGULATION OF T CELL PROLIFERATION | 76 | -0.23 | -0.88 | 0.640 | 0.887 | 1.000 | 3350 | tags=21%, list=16%, signal=25% | |
2263 | BMP SIGNALING PATHWAY | 48 | -0.24 | -0.88 | 0.674 | 0.887 | 1.000 | 4850 | tags=31%, list=24%, signal=41% | |
2264 | CHOLESTEROL METABOLIC PROCESS | 50 | -0.24 | -0.88 | 0.676 | 0.887 | 1.000 | 4498 | tags=24%, list=22%, signal=31% | |
2265 | EPITHELIAL CELL DIFFERENTIATION INVOLVED IN PROSTATE GLAND DEVELOPMENT | 12 | -0.30 | -0.88 | 0.654 | 0.888 | 1.000 | 5357 | tags=42%, list=26%, signal=56% | |
2266 | DIVALENT INORGANIC ANION HOMEOSTASIS | 10 | -0.35 | -0.88 | 0.625 | 0.888 | 1.000 | 6270 | tags=50%, list=30%, signal=72% | |
2267 | NEGATIVE REGULATION OF HORMONE METABOLIC PROCESS | 6 | -0.43 | -0.88 | 0.633 | 0.888 | 1.000 | 5050 | tags=50%, list=25%, signal=66% | |
2268 | T CELL DIFFERENTIATION IN THYMUS | 55 | -0.23 | -0.88 | 0.690 | 0.889 | 1.000 | 5275 | tags=31%, list=26%, signal=41% | |
2269 | THYMOCYTE AGGREGATION | 55 | -0.23 | -0.88 | 0.690 | 0.889 | 1.000 | 5275 | tags=31%, list=26%, signal=41% | |
2270 | NEGATIVE REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 143 | -0.21 | -0.88 | 0.699 | 0.889 | 1.000 | 7691 | tags=43%, list=37%, signal=68% | |
2271 | REGULATION OF RESPIRATORY GASEOUS EXCHANGE BY NEUROLOGICAL SYSTEM PROCESS | 5 | -0.45 | -0.88 | 0.641 | 0.888 | 1.000 | 2052 | tags=20%, list=10%, signal=22% | |
2272 | NEGATIVE REGULATION OF NEURON PROJECTION DEVELOPMENT | 83 | -0.22 | -0.88 | 0.682 | 0.888 | 1.000 | 6427 | tags=39%, list=31%, signal=56% | |
2273 | PEPTIDYL-LYSINE MONOMETHYLATION | 6 | -0.40 | -0.87 | 0.625 | 0.889 | 1.000 | 2806 | tags=33%, list=14%, signal=39% | |
2274 | CELLULAR RESPONSE TO CORTICOSTEROID STIMULUS | 8 | -0.38 | -0.87 | 0.633 | 0.888 | 1.000 | 108 | tags=13%, list=1%, signal=13% | |
2275 | EPITHELIAL CELL FATE COMMITMENT | 17 | -0.31 | -0.87 | 0.621 | 0.888 | 1.000 | 1322 | tags=18%, list=6%, signal=19% | |
2276 | PURINE NUCLEOTIDE METABOLIC PROCESS | 179 | -0.20 | -0.87 | 0.695 | 0.889 | 1.000 | 4407 | tags=22%, list=21%, signal=27% | |
2277 | REGULATION OF POTASSIUM ION TRANSMEMBRANE TRANSPORT | 45 | -0.24 | -0.87 | 0.649 | 0.888 | 1.000 | 7110 | tags=42%, list=35%, signal=64% | |
2278 | REGULATION OF ACTIVIN RECEPTOR SIGNALING PATHWAY | 16 | -0.29 | -0.87 | 0.622 | 0.888 | 1.000 | 4745 | tags=44%, list=23%, signal=57% | |
2279 | GLYCINE METABOLIC PROCESS | 9 | -0.36 | -0.87 | 0.589 | 0.888 | 1.000 | 6895 | tags=56%, list=33%, signal=83% | |
2280 | POSITIVE REGULATION OF TOR SIGNALING | 15 | -0.30 | -0.87 | 0.654 | 0.888 | 1.000 | 3474 | tags=33%, list=17%, signal=40% | |
2281 | POSITIVE REGULATION OF OXIDOREDUCTASE ACTIVITY | 32 | -0.25 | -0.87 | 0.649 | 0.888 | 1.000 | 6719 | tags=41%, list=33%, signal=60% | |
2282 | REGULATION OF CELL MIGRATION | 416 | -0.19 | -0.87 | 0.749 | 0.889 | 1.000 | 3312 | tags=18%, list=16%, signal=21% | |
2283 | REGULATION OF NEUTROPHIL CHEMOTAXIS | 16 | -0.31 | -0.87 | 0.650 | 0.888 | 1.000 | 794 | tags=13%, list=4%, signal=13% | |
2284 | RETINAL CONE CELL DIFFERENTIATION | 10 | -0.32 | -0.87 | 0.612 | 0.890 | 1.000 | 4908 | tags=40%, list=24%, signal=52% | |
2285 | RETINAL CONE CELL DEVELOPMENT | 10 | -0.32 | -0.87 | 0.612 | 0.890 | 1.000 | 4908 | tags=40%, list=24%, signal=52% | |
2286 | IMMUNE RESPONSE-INHIBITING SIGNAL TRANSDUCTION | 5 | -0.49 | -0.87 | 0.646 | 0.891 | 1.000 | 94 | tags=20%, list=0%, signal=20% | |
2287 | IMMUNE RESPONSE-INHIBITING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 5 | -0.49 | -0.87 | 0.646 | 0.891 | 1.000 | 94 | tags=20%, list=0%, signal=20% | |
2288 | EMBRYONIC CRANIAL SKELETON MORPHOGENESIS | 45 | -0.23 | -0.87 | 0.677 | 0.890 | 1.000 | 6656 | tags=42%, list=32%, signal=62% | |
2289 | REGULATION OF MEMBRANE PROTEIN ECTODOMAIN PROTEOLYSIS | 17 | -0.31 | -0.87 | 0.621 | 0.890 | 1.000 | 2893 | tags=24%, list=14%, signal=27% | |
2290 | EPITHELIAL CELL DEVELOPMENT | 188 | -0.19 | -0.87 | 0.732 | 0.890 | 1.000 | 5944 | tags=33%, list=29%, signal=46% | |
2291 | MORPHOGENESIS OF EMBRYONIC EPITHELIUM | 140 | -0.19 | -0.87 | 0.804 | 0.890 | 1.000 | 6537 | tags=37%, list=32%, signal=54% | |
2292 | REGULATION OF ESTABLISHMENT OF PLANAR POLARITY INVOLVED IN NEURAL TUBE CLOSURE | 13 | -0.33 | -0.87 | 0.623 | 0.889 | 1.000 | 3234 | tags=31%, list=16%, signal=36% | |
2293 | PLANAR CELL POLARITY PATHWAY INVOLVED IN NEURAL TUBE CLOSURE | 13 | -0.33 | -0.87 | 0.623 | 0.889 | 1.000 | 3234 | tags=31%, list=16%, signal=36% | |
2294 | VISUAL LEARNING | 10 | -0.34 | -0.87 | 0.619 | 0.889 | 1.000 | 9352 | tags=70%, list=45%, signal=128% | |
2295 | NEGATIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 416 | -0.18 | -0.87 | 0.792 | 0.888 | 1.000 | 4993 | tags=25%, list=24%, signal=32% | |
2296 | NEGATIVE REGULATION OF NEURON APOPTOTIC PROCESS | 46 | -0.22 | -0.87 | 0.730 | 0.889 | 1.000 | 4384 | tags=24%, list=21%, signal=30% | |
2297 | UNSATURATED FATTY ACID METABOLIC PROCESS | 69 | -0.24 | -0.87 | 0.648 | 0.889 | 1.000 | 3072 | tags=20%, list=15%, signal=24% | |
2298 | CHONDROITIN SULFATE METABOLIC PROCESS | 35 | -0.27 | -0.87 | 0.665 | 0.889 | 1.000 | 4434 | tags=31%, list=22%, signal=40% | |
2299 | REGULATION OF RECEPTOR BINDING | 14 | -0.29 | -0.87 | 0.642 | 0.889 | 1.000 | 3799 | tags=21%, list=18%, signal=26% | |
2300 | POSITIVE REGULATION OF CELLULAR COMPONENT MOVEMENT | 255 | -0.20 | -0.87 | 0.735 | 0.889 | 1.000 | 3293 | tags=18%, list=16%, signal=21% | |
2301 | POSITIVE REGULATION OF ALPHA-BETA T CELL ACTIVATION | 30 | -0.26 | -0.87 | 0.665 | 0.889 | 1.000 | 3650 | tags=27%, list=18%, signal=32% | |
2302 | REGULATION OF AMINE TRANSPORT | 23 | -0.28 | -0.87 | 0.615 | 0.890 | 1.000 | 160 | tags=9%, list=1%, signal=9% | |
2303 | CARDIAC MUSCLE TISSUE MORPHOGENESIS | 50 | -0.25 | -0.87 | 0.642 | 0.889 | 1.000 | 2252 | tags=16%, list=11%, signal=18% | |
2304 | REGULATION OF ANION TRANSMEMBRANE TRANSPORT | 16 | -0.30 | -0.87 | 0.663 | 0.889 | 1.000 | 5990 | tags=31%, list=29%, signal=44% | |
2305 | REGULATION OF HYDROGEN PEROXIDE-INDUCED CELL DEATH | 14 | -0.29 | -0.87 | 0.666 | 0.889 | 1.000 | 3533 | tags=36%, list=17%, signal=43% | |
2306 | REGULATION OF LYMPHOCYTE MIGRATION | 28 | -0.30 | -0.87 | 0.627 | 0.889 | 1.000 | 26 | tags=7%, list=0%, signal=7% | |
2307 | RESPONSE TO ESTRADIOL | 22 | -0.27 | -0.87 | 0.675 | 0.890 | 1.000 | 1331 | tags=14%, list=6%, signal=15% | |
2308 | REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 43 | -0.24 | -0.87 | 0.682 | 0.890 | 1.000 | 7094 | tags=44%, list=34%, signal=67% | |
2309 | REGULATION OF CELLULAR COMPONENT MOVEMENT | 481 | -0.19 | -0.87 | 0.789 | 0.890 | 1.000 | 5650 | tags=28%, list=27%, signal=38% | |
2310 | REGULATION OF ENERGY HOMEOSTASIS | 13 | -0.32 | -0.87 | 0.639 | 0.890 | 1.000 | 3690 | tags=38%, list=18%, signal=47% | |
2311 | 3'-UTR-MEDIATED MRNA STABILIZATION | 9 | -0.33 | -0.87 | 0.613 | 0.890 | 1.000 | 2757 | tags=22%, list=13%, signal=26% | |
2312 | PROTEIN TRIMERIZATION | 19 | -0.32 | -0.87 | 0.615 | 0.890 | 1.000 | 2535 | tags=26%, list=12%, signal=30% | |
2313 | REGULATION OF CHOLESTEROL STORAGE | 12 | -0.36 | -0.87 | 0.640 | 0.890 | 1.000 | 2933 | tags=25%, list=14%, signal=29% | |
2314 | REGULATION OF PRI-MIRNA TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 12 | -0.33 | -0.87 | 0.643 | 0.890 | 1.000 | 7277 | tags=50%, list=35%, signal=77% | |
2315 | POSITIVE REGULATION OF CARDIAC MUSCLE CONTRACTION | 6 | -0.41 | -0.87 | 0.672 | 0.891 | 1.000 | 5243 | tags=50%, list=25%, signal=67% | |
2316 | OLFACTORY BULB INTERNEURON DEVELOPMENT | 8 | -0.38 | -0.87 | 0.639 | 0.891 | 1.000 | 2062 | tags=25%, list=10%, signal=28% | |
2317 | REGULATION OF IMMUNOGLOBULIN SECRETION | 7 | -0.37 | -0.87 | 0.639 | 0.892 | 1.000 | 5743 | tags=43%, list=28%, signal=59% | |
2318 | POSITIVE REGULATION OF IMMUNOGLOBULIN SECRETION | 7 | -0.37 | -0.87 | 0.639 | 0.891 | 1.000 | 5743 | tags=43%, list=28%, signal=59% | |
2319 | REGULATION OF PROTEIN TARGETING TO MEMBRANE | 10 | -0.37 | -0.86 | 0.655 | 0.893 | 1.000 | 125 | tags=10%, list=1%, signal=10% | |
2320 | ODONTOGENESIS | 83 | -0.22 | -0.86 | 0.686 | 0.892 | 1.000 | 4559 | tags=27%, list=22%, signal=34% | |
2321 | REGULATION OF CALCIUM ION TRANSPORT INTO CYTOSOL | 54 | -0.23 | -0.86 | 0.689 | 0.892 | 1.000 | 5264 | tags=30%, list=26%, signal=40% | |
2322 | RETINAL GANGLION CELL AXON GUIDANCE | 19 | -0.28 | -0.86 | 0.670 | 0.892 | 1.000 | 2669 | tags=21%, list=13%, signal=24% | |
2323 | FOREBRAIN NEUROBLAST DIVISION | 8 | -0.36 | -0.86 | 0.675 | 0.892 | 1.000 | 1609 | tags=25%, list=8%, signal=27% | |
2324 | REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 28 | -0.27 | -0.86 | 0.678 | 0.891 | 1.000 | 4049 | tags=32%, list=20%, signal=40% | |
2325 | REGULATION OF ATP METABOLIC PROCESS | 28 | -0.27 | -0.86 | 0.678 | 0.891 | 1.000 | 4049 | tags=32%, list=20%, signal=40% | |
2326 | PURINE RIBONUCLEOSIDE BISPHOSPHATE METABOLIC PROCESS | 18 | -0.29 | -0.86 | 0.647 | 0.891 | 1.000 | 6781 | tags=50%, list=33%, signal=74% | |
2327 | 3'-PHOSPHOADENOSINE 5'-PHOSPHOSULFATE METABOLIC PROCESS | 18 | -0.29 | -0.86 | 0.647 | 0.891 | 1.000 | 6781 | tags=50%, list=33%, signal=74% | |
2328 | SNRNA PROCESSING | 12 | -0.35 | -0.86 | 0.645 | 0.890 | 1.000 | 5129 | tags=42%, list=25%, signal=55% | |
2329 | CELL COMMUNICATION BY ELECTRICAL COUPLING INVOLVED IN CARDIAC CONDUCTION | 11 | -0.33 | -0.86 | 0.639 | 0.890 | 1.000 | 4089 | tags=36%, list=20%, signal=45% | |
2330 | POSITIVE REGULATION OF MEMBRANE PROTEIN ECTODOMAIN PROTEOLYSIS | 13 | -0.32 | -0.86 | 0.635 | 0.890 | 1.000 | 2893 | tags=23%, list=14%, signal=27% | |
2331 | POSITIVE REGULATION OF CELL MIGRATION | 243 | -0.20 | -0.86 | 0.760 | 0.890 | 1.000 | 3293 | tags=18%, list=16%, signal=21% | |
2332 | POSITIVE REGULATION OF MALE GONAD DEVELOPMENT | 5 | -0.43 | -0.86 | 0.632 | 0.890 | 1.000 | 4634 | tags=60%, list=22%, signal=77% | |
2333 | NEGATIVE REGULATION OF ACTIVIN RECEPTOR SIGNALING PATHWAY | 8 | -0.34 | -0.86 | 0.631 | 0.890 | 1.000 | 4745 | tags=50%, list=23%, signal=65% | |
2334 | POST-EMBRYONIC MORPHOGENESIS | 16 | -0.28 | -0.86 | 0.649 | 0.889 | 1.000 | 5856 | tags=38%, list=28%, signal=52% | |
2335 | FATTY ACID BIOSYNTHETIC PROCESS | 50 | -0.24 | -0.86 | 0.685 | 0.889 | 1.000 | 2623 | tags=18%, list=13%, signal=21% | |
2336 | REGULATION OF B CELL ACTIVATION | 50 | -0.23 | -0.86 | 0.700 | 0.889 | 1.000 | 3350 | tags=22%, list=16%, signal=26% | |
2337 | RESPONSE TO INTERLEUKIN-1 | 48 | -0.24 | -0.86 | 0.699 | 0.889 | 1.000 | 3172 | tags=21%, list=15%, signal=25% | |
2338 | POSITIVE REGULATION OF NEUTROPHIL MIGRATION | 14 | -0.33 | -0.86 | 0.662 | 0.889 | 1.000 | 794 | tags=14%, list=4%, signal=15% | |
2339 | REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 85 | -0.23 | -0.86 | 0.666 | 0.889 | 1.000 | 6988 | tags=40%, list=34%, signal=60% | |
2340 | MONOSACCHARIDE BIOSYNTHETIC PROCESS | 42 | -0.26 | -0.86 | 0.623 | 0.889 | 1.000 | 287 | tags=7%, list=1%, signal=7% | |
2341 | POSITIVE REGULATION OF RAS PROTEIN SIGNAL TRANSDUCTION | 20 | -0.29 | -0.86 | 0.677 | 0.889 | 1.000 | 3815 | tags=35%, list=19%, signal=43% | |
2342 | CELLULAR RESPONSE TO VIRUS | 11 | -0.39 | -0.86 | 0.633 | 0.890 | 1.000 | 1711 | tags=27%, list=8%, signal=30% | |
2343 | REGULATION OF DNA REPLICATION | 109 | -0.24 | -0.86 | 0.663 | 0.890 | 1.000 | 4742 | tags=29%, list=23%, signal=38% | |
2344 | BRANCHING INVOLVED IN MAMMARY GLAND DUCT MORPHOGENESIS | 24 | -0.27 | -0.86 | 0.668 | 0.891 | 1.000 | 7581 | tags=46%, list=37%, signal=72% | |
2345 | PURINE-CONTAINING COMPOUND TRANSMEMBRANE TRANSPORT | 9 | -0.31 | -0.86 | 0.639 | 0.891 | 1.000 | 5619 | tags=33%, list=27%, signal=46% | |
2346 | POSITIVE REGULATION OF LYMPHOCYTE PROLIFERATION | 71 | -0.22 | -0.86 | 0.710 | 0.891 | 1.000 | 3350 | tags=20%, list=16%, signal=23% | |
2347 | SOCIAL BEHAVIOR | 21 | -0.28 | -0.86 | 0.638 | 0.891 | 1.000 | 4719 | tags=33%, list=23%, signal=43% | |
2348 | INTRASPECIES INTERACTION BETWEEN ORGANISMS | 21 | -0.28 | -0.86 | 0.638 | 0.891 | 1.000 | 4719 | tags=33%, list=23%, signal=43% | |
2349 | LEUKOCYTE TETHERING OR ROLLING | 11 | -0.35 | -0.86 | 0.644 | 0.891 | 1.000 | 251 | tags=9%, list=1%, signal=9% | |
2350 | PROTEIN MATURATION BY PROTEIN FOLDING | 5 | -0.43 | -0.86 | 0.659 | 0.891 | 1.000 | 2053 | tags=20%, list=10%, signal=22% | |
2351 | POSITIVE REGULATION OF EXCITATORY POSTSYNAPTIC POTENTIAL | 15 | -0.34 | -0.86 | 0.617 | 0.891 | 1.000 | 7611 | tags=60%, list=37%, signal=95% | |
2352 | ENERGY RESERVE METABOLIC PROCESS | 121 | -0.19 | -0.86 | 0.732 | 0.893 | 1.000 | 7037 | tags=35%, list=34%, signal=52% | |
2353 | HEXOSE TRANSMEMBRANE TRANSPORT | 8 | -0.34 | -0.86 | 0.652 | 0.893 | 1.000 | 8281 | tags=50%, list=40%, signal=84% | |
2354 | GLUCOSE TRANSMEMBRANE TRANSPORT | 8 | -0.34 | -0.86 | 0.652 | 0.893 | 1.000 | 8281 | tags=50%, list=40%, signal=84% | |
2355 | REGULATION OF NEUTROPHIL MIGRATION | 17 | -0.31 | -0.86 | 0.644 | 0.893 | 1.000 | 794 | tags=12%, list=4%, signal=12% | |
2356 | REGULATION OF LIPID KINASE ACTIVITY | 29 | -0.28 | -0.86 | 0.687 | 0.893 | 1.000 | 5650 | tags=34%, list=27%, signal=47% | |
2357 | POSITIVE REGULATION OF LIPID STORAGE | 11 | -0.35 | -0.86 | 0.648 | 0.892 | 1.000 | 2358 | tags=27%, list=11%, signal=31% | |
2358 | SOMATIC STEM CELL DIVISION | 16 | -0.28 | -0.86 | 0.709 | 0.892 | 1.000 | 5673 | tags=31%, list=28%, signal=43% | |
2359 | NEGATIVE REGULATION OF POTASSIUM ION TRANSMEMBRANE TRANSPORT | 15 | -0.30 | -0.86 | 0.659 | 0.893 | 1.000 | 4269 | tags=33%, list=21%, signal=42% | |
2360 | RESPONSE TO CAFFEINE | 6 | -0.39 | -0.86 | 0.649 | 0.893 | 1.000 | 6521 | tags=50%, list=32%, signal=73% | |
2361 | CELLULAR RESPONSE TO CAFFEINE | 6 | -0.39 | -0.86 | 0.649 | 0.892 | 1.000 | 6521 | tags=50%, list=32%, signal=73% | |
2362 | CELLULAR RESPONSE TO PURINE-CONTAINING COMPOUND | 6 | -0.39 | -0.86 | 0.649 | 0.892 | 1.000 | 6521 | tags=50%, list=32%, signal=73% | |
2363 | REGULATION OF GENE SILENCING | 19 | -0.27 | -0.86 | 0.660 | 0.892 | 1.000 | 1097 | tags=11%, list=5%, signal=11% | |
2364 | NEGATIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 316 | -0.19 | -0.86 | 0.779 | 0.892 | 1.000 | 4591 | tags=24%, list=22%, signal=30% | |
2365 | NEGATIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 316 | -0.19 | -0.86 | 0.779 | 0.891 | 1.000 | 4591 | tags=24%, list=22%, signal=30% | |
2366 | REGULATION OF HOMOTYPIC CELL-CELL ADHESION | 184 | -0.20 | -0.86 | 0.763 | 0.892 | 1.000 | 5743 | tags=31%, list=28%, signal=43% | |
2367 | MODULATION BY HOST OF VIRAL TRANSCRIPTION | 19 | -0.30 | -0.86 | 0.641 | 0.892 | 1.000 | 4909 | tags=32%, list=24%, signal=41% | |
2368 | MODULATION OF TRANSCRIPTION IN OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 19 | -0.30 | -0.86 | 0.641 | 0.892 | 1.000 | 4909 | tags=32%, list=24%, signal=41% | |
2369 | MODULATION BY HOST OF SYMBIONT TRANSCRIPTION | 19 | -0.30 | -0.86 | 0.641 | 0.891 | 1.000 | 4909 | tags=32%, list=24%, signal=41% | |
2370 | BRONCHUS DEVELOPMENT | 9 | -0.35 | -0.86 | 0.620 | 0.891 | 1.000 | 4586 | tags=33%, list=22%, signal=43% | |
2371 | REGULATION OF CELL ADHESION | 377 | -0.19 | -0.86 | 0.808 | 0.891 | 1.000 | 3124 | tags=18%, list=15%, signal=20% | |
2372 | DNA DEAMINATION | 8 | -0.38 | -0.86 | 0.642 | 0.891 | 1.000 | 333 | tags=13%, list=2%, signal=13% | |
2373 | RESPONSE TO CAMP | 31 | -0.26 | -0.86 | 0.663 | 0.891 | 1.000 | 5264 | tags=32%, list=26%, signal=43% | |
2374 | REGULATION OF NITRIC-OXIDE SYNTHASE ACTIVITY | 37 | -0.24 | -0.86 | 0.674 | 0.891 | 1.000 | 7138 | tags=38%, list=35%, signal=58% | |
2375 | CELL PROLIFERATION | 440 | -0.18 | -0.86 | 0.839 | 0.890 | 1.000 | 5807 | tags=30%, list=28%, signal=40% | |
2376 | CELLULAR RESPONSE TO ORGANIC CYCLIC COMPOUND | 170 | -0.19 | -0.85 | 0.777 | 0.891 | 1.000 | 4914 | tags=24%, list=24%, signal=31% | |
2377 | BILE ACID AND BILE SALT TRANSPORT | 19 | -0.29 | -0.85 | 0.667 | 0.892 | 1.000 | 2655 | tags=16%, list=13%, signal=18% | |
2378 | REGULATION OF CALCIUM ION-DEPENDENT EXOCYTOSIS | 22 | -0.28 | -0.85 | 0.661 | 0.891 | 1.000 | 3091 | tags=27%, list=15%, signal=32% | |
2379 | REGULATION OF ERK1 AND ERK2 CASCADE | 135 | -0.21 | -0.85 | 0.738 | 0.891 | 1.000 | 5825 | tags=33%, list=28%, signal=45% | |
2380 | NEGATIVE REGULATION OF CELL KILLING | 12 | -0.34 | -0.85 | 0.607 | 0.891 | 1.000 | 682 | tags=17%, list=3%, signal=17% | |
2381 | CHEMICAL HOMEOSTASIS | 462 | -0.18 | -0.85 | 0.797 | 0.891 | 1.000 | 4894 | tags=25%, list=24%, signal=32% | |
2382 | NEGATIVE REGULATION OF REPRODUCTIVE PROCESS | 18 | -0.30 | -0.85 | 0.668 | 0.890 | 1.000 | 2154 | tags=28%, list=10%, signal=31% | |
2383 | POSITIVE REGULATION OF HISTONE H3-K9 METHYLATION | 5 | -0.44 | -0.85 | 0.655 | 0.890 | 1.000 | 5189 | tags=60%, list=25%, signal=80% | |
2384 | POSITIVE REGULATION OF TRIGLYCERIDE METABOLIC PROCESS | 12 | -0.36 | -0.85 | 0.653 | 0.891 | 1.000 | 4193 | tags=33%, list=20%, signal=42% | |
2385 | POSITIVE REGULATION OF STEROID HORMONE SECRETION | 6 | -0.41 | -0.85 | 0.662 | 0.891 | 1.000 | 6961 | tags=67%, list=34%, signal=101% | |
2386 | NEGATIVE REGULATION OF MEIOTIC CELL CYCLE | 7 | -0.38 | -0.85 | 0.666 | 0.891 | 1.000 | 1967 | tags=29%, list=10%, signal=32% | |
2387 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA2 PRODUCTION | 6 | -0.38 | -0.85 | 0.680 | 0.891 | 1.000 | 294 | tags=17%, list=1%, signal=17% | |
2388 | REGULATION OF POTASSIUM ION TRANSPORT | 53 | -0.23 | -0.85 | 0.710 | 0.891 | 1.000 | 7871 | tags=47%, list=38%, signal=76% | |
2389 | POSITIVE REGULATION OF CELL FATE COMMITMENT | 7 | -0.38 | -0.85 | 0.637 | 0.891 | 1.000 | 5365 | tags=43%, list=26%, signal=58% | |
2390 | NEPHRIC DUCT MORPHOGENESIS | 11 | -0.35 | -0.85 | 0.649 | 0.891 | 1.000 | 7204 | tags=64%, list=35%, signal=98% | |
2391 | ATRIAL SEPTUM MORPHOGENESIS | 14 | -0.28 | -0.85 | 0.657 | 0.891 | 1.000 | 4163 | tags=29%, list=20%, signal=36% | |
2392 | REGULATION OF B CELL MEDIATED IMMUNITY | 17 | -0.28 | -0.85 | 0.709 | 0.891 | 1.000 | 7124 | tags=47%, list=35%, signal=72% | |
2393 | POSITIVE REGULATION OF CELL MOTILITY | 248 | -0.19 | -0.85 | 0.791 | 0.891 | 1.000 | 3293 | tags=18%, list=16%, signal=21% | |
2394 | VASCULAR SMOOTH MUSCLE CELL DIFFERENTIATION | 13 | -0.30 | -0.85 | 0.662 | 0.892 | 1.000 | 6421 | tags=38%, list=31%, signal=56% | |
2395 | NEGATIVE REGULATION OF CYCLIC NUCLEOTIDE METABOLIC PROCESS | 23 | -0.28 | -0.85 | 0.649 | 0.892 | 1.000 | 5264 | tags=39%, list=26%, signal=52% | |
2396 | POSITIVE REGULATION OF INFLAMMATORY RESPONSE | 36 | -0.25 | -0.85 | 0.682 | 0.891 | 1.000 | 3878 | tags=28%, list=19%, signal=34% | |
2397 | STEROID METABOLIC PROCESS | 146 | -0.20 | -0.85 | 0.736 | 0.892 | 1.000 | 7372 | tags=41%, list=36%, signal=64% | |
2398 | NEURONAL STEM CELL DIVISION | 13 | -0.31 | -0.85 | 0.706 | 0.891 | 1.000 | 5673 | tags=38%, list=28%, signal=53% | |
2399 | NEUROBLAST DIVISION | 13 | -0.31 | -0.85 | 0.706 | 0.891 | 1.000 | 5673 | tags=38%, list=28%, signal=53% | |
2400 | POSTTRANSCRIPTIONAL GENE SILENCING BY RNA | 26 | -0.29 | -0.85 | 0.663 | 0.891 | 1.000 | 2757 | tags=23%, list=13%, signal=27% | |
2401 | POSITIVE REGULATION OF THE FORCE OF HEART CONTRACTION | 5 | -0.39 | -0.85 | 0.660 | 0.891 | 1.000 | 945 | tags=20%, list=5%, signal=21% | |
2402 | PHOSPHATIDYLINOSITOL ACYL-CHAIN REMODELING | 13 | -0.33 | -0.85 | 0.631 | 0.891 | 1.000 | 6630 | tags=46%, list=32%, signal=68% | |
2403 | POSITIVE REGULATION OF FIBROBLAST APOPTOTIC PROCESS | 5 | -0.43 | -0.85 | 0.660 | 0.892 | 1.000 | 523 | tags=20%, list=3%, signal=21% | |
2404 | RESPONSE TO MUSCLE STRETCH | 9 | -0.35 | -0.85 | 0.626 | 0.892 | 1.000 | 5630 | tags=44%, list=27%, signal=61% | |
2405 | PYRIDINE-CONTAINING COMPOUND METABOLIC PROCESS | 59 | -0.24 | -0.85 | 0.683 | 0.892 | 1.000 | 4874 | tags=27%, list=24%, signal=35% | |
2406 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 20 | -0.29 | -0.85 | 0.680 | 0.892 | 1.000 | 3961 | tags=35%, list=19%, signal=43% | |
2407 | ESTROGEN METABOLIC PROCESS | 9 | -0.33 | -0.85 | 0.645 | 0.892 | 1.000 | 9570 | tags=67%, list=46%, signal=124% | |
2408 | NEGATIVE REGULATION OF AMINE TRANSPORT | 6 | -0.41 | -0.85 | 0.652 | 0.892 | 1.000 | 160 | tags=17%, list=1%, signal=17% | |
2409 | REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 126 | -0.20 | -0.85 | 0.747 | 0.892 | 1.000 | 3689 | tags=20%, list=18%, signal=24% | |
2410 | POSITIVE REGULATION OF GRANULOCYTE CHEMOTAXIS | 15 | -0.30 | -0.85 | 0.677 | 0.893 | 1.000 | 2597 | tags=20%, list=13%, signal=23% | |
2411 | POSITIVE REGULATION OF KERATINOCYTE DIFFERENTIATION | 7 | -0.34 | -0.85 | 0.691 | 0.893 | 1.000 | 1793 | tags=29%, list=9%, signal=31% | |
2412 | L-SERINE METABOLIC PROCESS | 8 | -0.39 | -0.85 | 0.636 | 0.894 | 1.000 | 3910 | tags=38%, list=19%, signal=46% | |
2413 | REGULATION OF RETINOIC ACID RECEPTOR SIGNALING PATHWAY | 10 | -0.34 | -0.85 | 0.664 | 0.893 | 1.000 | 108 | tags=10%, list=1%, signal=10% | |
2414 | FATTY ACID METABOLIC PROCESS | 147 | -0.21 | -0.85 | 0.707 | 0.894 | 1.000 | 3645 | tags=22%, list=18%, signal=27% | |
2415 | PROLINE TRANSPORT | 6 | -0.41 | -0.85 | 0.669 | 0.894 | 1.000 | 2954 | tags=33%, list=14%, signal=39% | |
2416 | NEGATIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 79 | -0.22 | -0.85 | 0.744 | 0.894 | 1.000 | 4566 | tags=29%, list=22%, signal=37% | |
2417 | MAMMARY DUCT TERMINAL END BUD GROWTH | 6 | -0.41 | -0.85 | 0.641 | 0.894 | 1.000 | 316 | tags=17%, list=2%, signal=17% | |
2418 | CARBOHYDRATE DERIVATIVE TRANSPORT | 27 | -0.25 | -0.84 | 0.706 | 0.894 | 1.000 | 2209 | tags=19%, list=11%, signal=21% | |
2419 | RENAL SYSTEM PROCESS | 66 | -0.21 | -0.84 | 0.739 | 0.894 | 1.000 | 7372 | tags=41%, list=36%, signal=63% | |
2420 | SINGLE-ORGANISM BEHAVIOR | 97 | -0.21 | -0.84 | 0.723 | 0.895 | 1.000 | 7254 | tags=39%, list=35%, signal=60% | |
2421 | HEART CONTRACTION | 48 | -0.24 | -0.84 | 0.704 | 0.895 | 1.000 | 4089 | tags=25%, list=20%, signal=31% | |
2422 | CELLULAR RESPONSE TO TOPOLOGICALLY INCORRECT PROTEIN | 96 | -0.23 | -0.84 | 0.653 | 0.894 | 1.000 | 3050 | tags=20%, list=15%, signal=23% | |
2423 | MORPHOGENESIS OF AN EPITHELIAL BUD | 9 | -0.33 | -0.84 | 0.693 | 0.894 | 1.000 | 4460 | tags=56%, list=22%, signal=71% | |
2424 | ATRIOVENTRICULAR VALVE DEVELOPMENT | 21 | -0.27 | -0.84 | 0.697 | 0.894 | 1.000 | 1462 | tags=14%, list=7%, signal=15% | |
2425 | POSTTRANSCRIPTIONAL GENE SILENCING | 27 | -0.29 | -0.84 | 0.665 | 0.895 | 1.000 | 2757 | tags=22%, list=13%, signal=26% | |
2426 | REGULATION OF T-HELPER 1 CELL DIFFERENTIATION | 6 | -0.38 | -0.84 | 0.676 | 0.894 | 1.000 | 5601 | tags=33%, list=27%, signal=46% | |
2427 | CHONDROBLAST DIFFERENTIATION | 5 | -0.42 | -0.84 | 0.660 | 0.896 | 1.000 | 4206 | tags=60%, list=20%, signal=75% | |
2428 | REGULATION OF WOUND HEALING | 79 | -0.23 | -0.84 | 0.705 | 0.896 | 1.000 | 6128 | tags=37%, list=30%, signal=52% | |
2429 | CELL COMMUNICATION BY ELECTRICAL COUPLING | 13 | -0.31 | -0.84 | 0.663 | 0.896 | 1.000 | 5039 | tags=38%, list=24%, signal=51% | |
2430 | REGULATION OF HEART RATE | 50 | -0.24 | -0.84 | 0.704 | 0.896 | 1.000 | 5637 | tags=36%, list=27%, signal=49% | |
2431 | AMINOGLYCAN METABOLIC PROCESS | 115 | -0.21 | -0.84 | 0.735 | 0.897 | 1.000 | 5484 | tags=30%, list=27%, signal=41% | |
2432 | IN UTERO EMBRYONIC DEVELOPMENT | 341 | -0.18 | -0.84 | 0.836 | 0.897 | 1.000 | 3858 | tags=19%, list=19%, signal=23% | |
2433 | POSITIVE REGULATION OF MONONUCLEAR CELL PROLIFERATION | 72 | -0.21 | -0.84 | 0.744 | 0.897 | 1.000 | 3350 | tags=19%, list=16%, signal=23% | |
2434 | SUBSTRATE-DEPENDENT CEREBRAL CORTEX TANGENTIAL MIGRATION | 5 | -0.42 | -0.84 | 0.670 | 0.897 | 1.000 | 1322 | tags=20%, list=6%, signal=21% | |
2435 | PLACENTA BLOOD VESSEL DEVELOPMENT | 31 | -0.25 | -0.84 | 0.693 | 0.897 | 1.000 | 2252 | tags=16%, list=11%, signal=18% | |
2436 | POSITIVE REGULATION OF ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 39 | -0.23 | -0.84 | 0.711 | 0.897 | 1.000 | 6561 | tags=36%, list=32%, signal=53% | |
2437 | RESPONSE TO UNFOLDED PROTEIN | 106 | -0.23 | -0.84 | 0.689 | 0.897 | 1.000 | 4323 | tags=25%, list=21%, signal=31% | |
2438 | PHOSPHATIDYLCHOLINE ACYL-CHAIN REMODELING | 20 | -0.29 | -0.84 | 0.672 | 0.897 | 1.000 | 2230 | tags=20%, list=11%, signal=22% | |
2439 | EPITHELIAL CELL MIGRATION | 53 | -0.25 | -0.84 | 0.697 | 0.897 | 1.000 | 2119 | tags=17%, list=10%, signal=19% | |
2440 | POSITIVE REGULATION OF INTERLEUKIN-4 PRODUCTION | 10 | -0.34 | -0.84 | 0.724 | 0.897 | 1.000 | 4557 | tags=40%, list=22%, signal=51% | |
2441 | INTRACELLULAR RECEPTOR SIGNALING PATHWAY | 105 | -0.20 | -0.84 | 0.722 | 0.898 | 1.000 | 3398 | tags=20%, list=16%, signal=24% | |
2442 | NUCLEOSIDE DIPHOSPHATE METABOLIC PROCESS | 44 | -0.26 | -0.84 | 0.684 | 0.898 | 1.000 | 1171 | tags=11%, list=6%, signal=12% | |
2443 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT5 PROTEIN | 15 | -0.28 | -0.84 | 0.692 | 0.898 | 1.000 | 8617 | tags=53%, list=42%, signal=92% | |
2444 | REGULATION OF CELL MOTILITY | 440 | -0.18 | -0.84 | 0.829 | 0.898 | 1.000 | 3312 | tags=17%, list=16%, signal=20% | |
2445 | CELLULAR ANION HOMEOSTASIS | 6 | -0.37 | -0.84 | 0.629 | 0.898 | 1.000 | 7087 | tags=67%, list=34%, signal=102% | |
2446 | CELLULAR MONOVALENT INORGANIC ANION HOMEOSTASIS | 6 | -0.37 | -0.84 | 0.629 | 0.898 | 1.000 | 7087 | tags=67%, list=34%, signal=102% | |
2447 | SKELETAL MUSCLE TISSUE REGENERATION | 20 | -0.26 | -0.84 | 0.708 | 0.898 | 1.000 | 5642 | tags=30%, list=27%, signal=41% | |
2448 | POSITIVE REGULATION OF CELL PROLIFERATION | 430 | -0.18 | -0.84 | 0.854 | 0.899 | 1.000 | 5515 | tags=27%, list=27%, signal=35% | |
2449 | T CELL DIFFERENTIATION | 135 | -0.20 | -0.84 | 0.772 | 0.899 | 1.000 | 5275 | tags=28%, list=26%, signal=38% | |
2450 | POSITIVE REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 21 | -0.27 | -0.84 | 0.737 | 0.900 | 1.000 | 3815 | tags=33%, list=19%, signal=41% | |
2451 | PHOSPHATIDYLCHOLINE METABOLIC PROCESS | 49 | -0.24 | -0.84 | 0.753 | 0.900 | 1.000 | 6630 | tags=41%, list=32%, signal=60% | |
2452 | VIRAL PROTEIN PROCESSING | 12 | -0.29 | -0.84 | 0.688 | 0.900 | 1.000 | 357 | tags=8%, list=2%, signal=8% | |
2453 | ENDOCARDIAL CUSHION DEVELOPMENT | 34 | -0.23 | -0.84 | 0.737 | 0.900 | 1.000 | 4163 | tags=24%, list=20%, signal=29% | |
2454 | RESPONSE TO GLUCAGON | 34 | -0.23 | -0.84 | 0.740 | 0.900 | 1.000 | 6582 | tags=41%, list=32%, signal=60% | |
2455 | PYRIDINE NUCLEOTIDE METABOLIC PROCESS | 53 | -0.24 | -0.83 | 0.684 | 0.901 | 1.000 | 4874 | tags=26%, list=24%, signal=35% | |
2456 | NICOTINAMIDE NUCLEOTIDE METABOLIC PROCESS | 53 | -0.24 | -0.83 | 0.684 | 0.900 | 1.000 | 4874 | tags=26%, list=24%, signal=35% | |
2457 | REGULATION OF STRIATED MUSCLE CELL DIFFERENTIATION | 41 | -0.25 | -0.83 | 0.717 | 0.900 | 1.000 | 7577 | tags=49%, list=37%, signal=77% | |
2458 | LEUKOCYTE MIGRATION | 180 | -0.20 | -0.83 | 0.789 | 0.900 | 1.000 | 3560 | tags=19%, list=17%, signal=23% | |
2459 | WHITE FAT CELL DIFFERENTIATION | 13 | -0.30 | -0.83 | 0.725 | 0.900 | 1.000 | 3988 | tags=31%, list=19%, signal=38% | |
2460 | NEUTROPHIL MEDIATED IMMUNITY | 9 | -0.37 | -0.83 | 0.669 | 0.900 | 1.000 | 1479 | tags=22%, list=7%, signal=24% | |
2461 | ACTIN FILAMENT ORGANIZATION | 83 | -0.21 | -0.83 | 0.718 | 0.900 | 1.000 | 4823 | tags=23%, list=23%, signal=30% | |
2462 | MONOCARBOXYLIC ACID BIOSYNTHETIC PROCESS | 86 | -0.22 | -0.83 | 0.751 | 0.900 | 1.000 | 3878 | tags=22%, list=19%, signal=27% | |
2463 | CILIARY NEUROTROPHIC FACTOR-MEDIATED SIGNALING PATHWAY | 5 | -0.43 | -0.83 | 0.696 | 0.899 | 1.000 | 1308 | tags=20%, list=6%, signal=21% | |
2464 | TISSUE MIGRATION | 62 | -0.23 | -0.83 | 0.697 | 0.899 | 1.000 | 3217 | tags=21%, list=16%, signal=25% | |
2465 | REGULATION OF ERYTHROCYTE DIFFERENTIATION | 19 | -0.29 | -0.83 | 0.706 | 0.899 | 1.000 | 925 | tags=16%, list=4%, signal=17% | |
2466 | REGULATION OF LOCOMOTION | 487 | -0.18 | -0.83 | 0.835 | 0.899 | 1.000 | 3312 | tags=17%, list=16%, signal=20% | |
2467 | NEGATIVE REGULATION OF VIRAL TRANSCRIPTION | 21 | -0.28 | -0.83 | 0.686 | 0.899 | 1.000 | 4909 | tags=38%, list=24%, signal=50% | |
2468 | REGULATION OF COLLAGEN METABOLIC PROCESS | 15 | -0.31 | -0.83 | 0.689 | 0.900 | 1.000 | 1877 | tags=20%, list=9%, signal=22% | |
2469 | REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 15 | -0.31 | -0.83 | 0.689 | 0.900 | 1.000 | 1877 | tags=20%, list=9%, signal=22% | |
2470 | ATF6-MEDIATED UNFOLDED PROTEIN RESPONSE | 8 | -0.38 | -0.83 | 0.673 | 0.900 | 1.000 | 7363 | tags=50%, list=36%, signal=78% | |
2471 | CARTILAGE MORPHOGENESIS | 11 | -0.32 | -0.83 | 0.688 | 0.901 | 1.000 | 3732 | tags=27%, list=18%, signal=33% | |
2472 | THROMBIN RECEPTOR SIGNALING PATHWAY | 6 | -0.42 | -0.83 | 0.668 | 0.901 | 1.000 | 2786 | tags=33%, list=14%, signal=39% | |
2473 | EXTRACELLULAR MATRIX DISASSEMBLY | 110 | -0.24 | -0.83 | 0.674 | 0.901 | 1.000 | 5912 | tags=36%, list=29%, signal=51% | |
2474 | REGULATION OF INTERLEUKIN-1 SECRETION | 15 | -0.28 | -0.83 | 0.685 | 0.901 | 1.000 | 794 | tags=13%, list=4%, signal=14% | |
2475 | PROTEOGLYCAN METABOLIC PROCESS | 53 | -0.24 | -0.83 | 0.702 | 0.901 | 1.000 | 3927 | tags=28%, list=19%, signal=35% | |
2476 | POSITIVE REGULATION OF PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 9 | -0.34 | -0.83 | 0.693 | 0.903 | 1.000 | 5264 | tags=44%, list=26%, signal=60% | |
2477 | RESPONSE TO DRUG | 103 | -0.19 | -0.83 | 0.845 | 0.902 | 1.000 | 6657 | tags=36%, list=32%, signal=53% | |
2478 | NUCLEOTIDE METABOLIC PROCESS | 233 | -0.19 | -0.83 | 0.779 | 0.904 | 1.000 | 3070 | tags=16%, list=15%, signal=18% | |
2479 | POSITIVE REGULATION OF DNA-DEPENDENT DNA REPLICATION | 9 | -0.37 | -0.83 | 0.701 | 0.904 | 1.000 | 7099 | tags=56%, list=34%, signal=85% | |
2480 | RIBOSOMAL SMALL SUBUNIT BIOGENESIS | 13 | -0.35 | -0.83 | 0.656 | 0.904 | 1.000 | 9674 | tags=62%, list=47%, signal=116% | |
2481 | CELLULAR RESPONSE TO LAMINAR FLUID SHEAR STRESS | 7 | -0.38 | -0.83 | 0.690 | 0.904 | 1.000 | 1637 | tags=29%, list=8%, signal=31% | |
2482 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO TELOMERE | 8 | -0.44 | -0.83 | 0.647 | 0.904 | 1.000 | 9666 | tags=63%, list=47%, signal=118% | |
2483 | REGULATION OF ATRIAL CARDIAC MUSCLE CELL MEMBRANE REPOLARIZATION | 5 | -0.43 | -0.83 | 0.694 | 0.904 | 1.000 | 5637 | tags=60%, list=27%, signal=83% | |
2484 | MESONEPHRIC TUBULE FORMATION | 9 | -0.31 | -0.83 | 0.709 | 0.904 | 1.000 | 6755 | tags=67%, list=33%, signal=99% | |
2485 | ASYMMETRIC NEUROBLAST DIVISION | 5 | -0.42 | -0.83 | 0.671 | 0.905 | 1.000 | 5511 | tags=40%, list=27%, signal=55% | |
2486 | OTIC VESICLE FORMATION | 9 | -0.34 | -0.83 | 0.697 | 0.905 | 1.000 | 4823 | tags=44%, list=23%, signal=58% | |
2487 | CELLULAR DIVALENT INORGANIC ANION HOMEOSTASIS | 5 | -0.38 | -0.83 | 0.663 | 0.905 | 1.000 | 5943 | tags=60%, list=29%, signal=84% | |
2488 | NEGATIVE REGULATION OF AXONOGENESIS | 45 | -0.24 | -0.83 | 0.707 | 0.905 | 1.000 | 7269 | tags=42%, list=35%, signal=65% | |
2489 | POSITIVE REGULATION OF ION TRANSMEMBRANE TRANSPORT | 69 | -0.22 | -0.83 | 0.727 | 0.905 | 1.000 | 6568 | tags=38%, list=32%, signal=55% | |
2490 | POSITIVE REGULATION OF POTASSIUM ION TRANSMEMBRANE TRANSPORT | 17 | -0.28 | -0.83 | 0.728 | 0.904 | 1.000 | 5264 | tags=35%, list=26%, signal=47% | |
2491 | POSITIVE REGULATION OF INTRACELLULAR STEROID HORMONE RECEPTOR SIGNALING PATHWAY | 7 | -0.32 | -0.83 | 0.719 | 0.904 | 1.000 | 5407 | tags=57%, list=26%, signal=77% | |
2492 | NEGATIVE REGULATION OF ADAPTIVE IMMUNE RESPONSE BASED ON SOMATIC RECOMBINATION OF IMMUNE RECEPTORS BUILT FROM IMMUNOGLOBULIN SUPERFAMILY DOMAINS | 16 | -0.28 | -0.83 | 0.723 | 0.904 | 1.000 | 3840 | tags=31%, list=19%, signal=38% | |
2493 | THYROID GLAND DEVELOPMENT | 25 | -0.27 | -0.83 | 0.705 | 0.904 | 1.000 | 4761 | tags=40%, list=23%, signal=52% | |
2494 | CHROMATIN SILENCING AT RDNA | 10 | -0.32 | -0.83 | 0.700 | 0.905 | 1.000 | 136 | tags=10%, list=1%, signal=10% | |
2495 | ENDOTHELIAL CELL CHEMOTAXIS | 8 | -0.41 | -0.83 | 0.675 | 0.905 | 1.000 | 2119 | tags=38%, list=10%, signal=42% | |
2496 | ADENYLATE CYCLASE-INHIBITING G-PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY | 39 | -0.24 | -0.83 | 0.734 | 0.905 | 1.000 | 6582 | tags=33%, list=32%, signal=49% | |
2497 | NEGATIVE REGULATION OF OSTEOBLAST PROLIFERATION | 5 | -0.39 | -0.82 | 0.684 | 0.904 | 1.000 | 3818 | tags=40%, list=19%, signal=49% | |
2498 | AXON REGENERATION | 12 | -0.35 | -0.82 | 0.687 | 0.905 | 1.000 | 6482 | tags=42%, list=31%, signal=61% | |
2499 | EYE PHOTORECEPTOR CELL DEVELOPMENT | 33 | -0.23 | -0.82 | 0.747 | 0.905 | 1.000 | 5650 | tags=39%, list=27%, signal=54% | |
2500 | POSITIVE REGULATION OF SYNAPSE ASSEMBLY | 13 | -0.31 | -0.82 | 0.686 | 0.905 | 1.000 | 7608 | tags=54%, list=37%, signal=85% | |
2501 | NEGATIVE REGULATION OF PHOSPHATASE ACTIVITY | 44 | -0.22 | -0.82 | 0.762 | 0.905 | 1.000 | 2053 | tags=16%, list=10%, signal=18% | |
2502 | REGULATION OF TRANSCRIPTION REGULATORY REGION DNA BINDING | 23 | -0.25 | -0.82 | 0.764 | 0.905 | 1.000 | 1746 | tags=13%, list=8%, signal=14% | |
2503 | POSITIVE REGULATION OF CATION CHANNEL ACTIVITY | 21 | -0.25 | -0.82 | 0.706 | 0.904 | 1.000 | 6561 | tags=38%, list=32%, signal=56% | |
2504 | 'DE NOVO' PROTEIN FOLDING | 34 | -0.28 | -0.82 | 0.612 | 0.905 | 1.000 | 3382 | tags=18%, list=16%, signal=21% | |
2505 | NEGATIVE REGULATION OF CAMP BIOSYNTHETIC PROCESS | 21 | -0.28 | -0.82 | 0.692 | 0.905 | 1.000 | 5264 | tags=38%, list=26%, signal=51% | |
2506 | REGULATION OF PHOSPHOLIPID TRANSPORT | 5 | -0.40 | -0.82 | 0.706 | 0.905 | 1.000 | 4010 | tags=40%, list=19%, signal=50% | |
2507 | POSITIVE REGULATION OF PHOSPHOLIPID TRANSPORT | 5 | -0.40 | -0.82 | 0.706 | 0.905 | 1.000 | 4010 | tags=40%, list=19%, signal=50% | |
2508 | REGULATION OF RHO PROTEIN SIGNAL TRANSDUCTION | 22 | -0.27 | -0.82 | 0.725 | 0.904 | 1.000 | 5243 | tags=32%, list=25%, signal=43% | |
2509 | REGULATION OF PROTEIN SUMOYLATION | 13 | -0.30 | -0.82 | 0.745 | 0.904 | 1.000 | 1263 | tags=15%, list=6%, signal=16% | |
2510 | NEGATIVE REGULATION OF SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 20 | -0.27 | -0.82 | 0.736 | 0.905 | 1.000 | 1120 | tags=15%, list=5%, signal=16% | |
2511 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 20 | -0.27 | -0.82 | 0.736 | 0.904 | 1.000 | 1120 | tags=15%, list=5%, signal=16% | |
2512 | SYNAPTIC VESICLE ENDOCYTOSIS | 8 | -0.36 | -0.82 | 0.690 | 0.904 | 1.000 | 1951 | tags=25%, list=9%, signal=28% | |
2513 | MACROMOLECULE METHYLATION | 97 | -0.22 | -0.82 | 0.714 | 0.904 | 1.000 | 3839 | tags=19%, list=19%, signal=23% | |
2514 | REGULATION OF CELL KILLING | 39 | -0.24 | -0.82 | 0.736 | 0.905 | 1.000 | 3208 | tags=18%, list=16%, signal=21% | |
2515 | CELLULAR RESPONSE TO CAMP | 25 | -0.26 | -0.82 | 0.734 | 0.905 | 1.000 | 5264 | tags=32%, list=26%, signal=43% | |
2516 | REGULATION OF PEPTIDYL-SERINE PHOSPHORYLATION | 65 | -0.21 | -0.82 | 0.775 | 0.905 | 1.000 | 4626 | tags=25%, list=22%, signal=32% | |
2517 | REGULATION OF FATTY ACID OXIDATION | 17 | -0.30 | -0.82 | 0.694 | 0.905 | 1.000 | 3690 | tags=29%, list=18%, signal=36% | |
2518 | ENTRAINMENT OF CIRCADIAN CLOCK | 19 | -0.26 | -0.82 | 0.750 | 0.905 | 1.000 | 5485 | tags=37%, list=27%, signal=50% | |
2519 | POSITIVE REGULATION OF B CELL ACTIVATION | 31 | -0.24 | -0.82 | 0.757 | 0.906 | 1.000 | 3350 | tags=23%, list=16%, signal=27% | |
2520 | REGULATION OF NEURON APOPTOTIC PROCESS | 69 | -0.20 | -0.82 | 0.761 | 0.907 | 1.000 | 5056 | tags=25%, list=25%, signal=33% | |
2521 | TUBE FORMATION | 135 | -0.18 | -0.82 | 0.888 | 0.907 | 1.000 | 6181 | tags=33%, list=30%, signal=47% | |
2522 | GANGLIOSIDE BIOSYNTHETIC PROCESS | 5 | -0.39 | -0.82 | 0.692 | 0.907 | 1.000 | 8098 | tags=80%, list=39%, signal=132% | |
2523 | REGULATION OF T CELL ACTIVATION VIA T CELL RECEPTOR CONTACT WITH ANTIGEN BOUND TO MHC MOLECULE ON ANTIGEN PRESENTING CELL | 5 | -0.43 | -0.82 | 0.697 | 0.907 | 1.000 | 5854 | tags=40%, list=28%, signal=56% | |
2524 | DRUG METABOLIC PROCESS | 26 | -0.25 | -0.82 | 0.713 | 0.907 | 1.000 | 5651 | tags=38%, list=27%, signal=53% | |
2525 | REGULATION OF PROTEIN K63-LINKED UBIQUITINATION | 6 | -0.38 | -0.82 | 0.701 | 0.907 | 1.000 | 7446 | tags=50%, list=36%, signal=78% | |
2526 | NEURON FATE DETERMINATION | 9 | -0.34 | -0.82 | 0.669 | 0.907 | 1.000 | 9706 | tags=67%, list=47%, signal=126% | |
2527 | NEGATIVE REGULATION OF HYDROGEN PEROXIDE-MEDIATED PROGRAMMED CELL DEATH | 5 | -0.39 | -0.82 | 0.719 | 0.907 | 1.000 | 5989 | tags=60%, list=29%, signal=85% | |
2528 | REGULATION OF SECRETION BY CELL | 327 | -0.17 | -0.82 | 0.853 | 0.908 | 1.000 | 3740 | tags=18%, list=18%, signal=22% | |
2529 | RRNA PROCESSING | 41 | -0.29 | -0.82 | 0.668 | 0.908 | 1.000 | 9224 | tags=56%, list=45%, signal=101% | |
2530 | NEURAL CREST CELL MIGRATION | 35 | -0.23 | -0.82 | 0.727 | 0.908 | 1.000 | 6537 | tags=46%, list=32%, signal=67% | |
2531 | POSITIVE REGULATION OF MUSCLE CONTRACTION | 13 | -0.31 | -0.82 | 0.710 | 0.908 | 1.000 | 5287 | tags=38%, list=26%, signal=52% | |
2532 | ACTIN CYTOSKELETON ORGANIZATION | 216 | -0.18 | -0.82 | 0.857 | 0.909 | 1.000 | 4913 | tags=24%, list=24%, signal=31% | |
2533 | REGULATION OF INTERLEUKIN-1 BETA SECRETION | 13 | -0.29 | -0.82 | 0.718 | 0.909 | 1.000 | 794 | tags=15%, list=4%, signal=16% | |
2534 | PURINE DEOXYRIBONUCLEOTIDE CATABOLIC PROCESS | 8 | -0.39 | -0.82 | 0.704 | 0.909 | 1.000 | 2575 | tags=25%, list=12%, signal=29% | |
2535 | CELL PROLIFERATION IN FOREBRAIN | 28 | -0.25 | -0.82 | 0.766 | 0.909 | 1.000 | 1609 | tags=14%, list=8%, signal=15% | |
2536 | POSITIVE REGULATION OF PROTEIN KINASE ACTIVITY | 427 | -0.18 | -0.82 | 0.850 | 0.909 | 1.000 | 6356 | tags=31%, list=31%, signal=44% | |
2537 | IMPORT INTO CELL | 14 | -0.29 | -0.81 | 0.723 | 0.912 | 1.000 | 4089 | tags=29%, list=20%, signal=36% | |
2538 | POSITIVE REGULATION OF SPROUTING ANGIOGENESIS | 10 | -0.31 | -0.81 | 0.737 | 0.912 | 1.000 | 6245 | tags=50%, list=30%, signal=72% | |
2539 | ACUTE-PHASE RESPONSE | 13 | -0.32 | -0.81 | 0.742 | 0.912 | 1.000 | 3303 | tags=31%, list=16%, signal=37% | |
2540 | C21-STEROID HORMONE METABOLIC PROCESS | 19 | -0.31 | -0.81 | 0.688 | 0.912 | 1.000 | 6059 | tags=42%, list=29%, signal=60% | |
2541 | PURINE RIBONUCLEOTIDE METABOLIC PROCESS | 157 | -0.18 | -0.81 | 0.830 | 0.913 | 1.000 | 2134 | tags=12%, list=10%, signal=13% | |
2542 | RIBONUCLEOTIDE METABOLIC PROCESS | 159 | -0.18 | -0.81 | 0.840 | 0.913 | 1.000 | 2134 | tags=12%, list=10%, signal=13% | |
2543 | REGULATION OF CALCINEURIN-NFAT SIGNALING CASCADE | 8 | -0.34 | -0.81 | 0.711 | 0.913 | 1.000 | 6254 | tags=38%, list=30%, signal=54% | |
2544 | RNA SPLICING, VIA ENDONUCLEOLYTIC CLEAVAGE AND LIGATION | 5 | -0.43 | -0.81 | 0.710 | 0.912 | 1.000 | 84 | tags=20%, list=0%, signal=20% | |
2545 | POST-EMBRYONIC EYE MORPHOGENESIS | 7 | -0.34 | -0.81 | 0.719 | 0.912 | 1.000 | 6892 | tags=57%, list=33%, signal=86% | |
2546 | REGULATION OF SHORT-TERM NEURONAL SYNAPTIC PLASTICITY | 7 | -0.38 | -0.81 | 0.688 | 0.912 | 1.000 | 6795 | tags=71%, list=33%, signal=107% | |
2547 | POSITIVE REGULATION OF GLIOGENESIS | 30 | -0.25 | -0.81 | 0.732 | 0.913 | 1.000 | 7076 | tags=50%, list=34%, signal=76% | |
2548 | PROTEIN STABILIZATION | 101 | -0.19 | -0.81 | 0.811 | 0.913 | 1.000 | 4384 | tags=23%, list=21%, signal=29% | |
2549 | POSITIVE REGULATION OF CALCIUM ION TRANSPORT INTO CYTOSOL | 29 | -0.25 | -0.81 | 0.742 | 0.913 | 1.000 | 5264 | tags=34%, list=26%, signal=46% | |
2550 | REGULATION OF RENAL SYSTEM PROCESS | 13 | -0.32 | -0.81 | 0.737 | 0.914 | 1.000 | 2379 | tags=23%, list=12%, signal=26% | |
2551 | POSITIVE REGULATION OF SEQUENCE-SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 176 | -0.19 | -0.81 | 0.794 | 0.914 | 1.000 | 4012 | tags=22%, list=19%, signal=27% | |
2552 | ESTABLISHMENT OF CELL POLARITY | 41 | -0.22 | -0.81 | 0.782 | 0.914 | 1.000 | 3692 | tags=22%, list=18%, signal=27% | |
2553 | POSITIVE REGULATION OF ACTION POTENTIAL | 5 | -0.39 | -0.81 | 0.718 | 0.914 | 1.000 | 5243 | tags=40%, list=25%, signal=54% | |
2554 | POSITIVE REGULATION OF SYNAPTIC TRANSMISSION | 38 | -0.25 | -0.81 | 0.701 | 0.914 | 1.000 | 6120 | tags=42%, list=30%, signal=60% | |
2555 | PATHWAY-RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 11 | -0.34 | -0.81 | 0.720 | 0.915 | 1.000 | 4281 | tags=27%, list=21%, signal=34% | |
2556 | NEGATIVE REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 20 | -0.27 | -0.81 | 0.741 | 0.916 | 1.000 | 6755 | tags=40%, list=33%, signal=59% | |
2557 | REGULATION OF B CELL RECEPTOR SIGNALING PATHWAY | 5 | -0.42 | -0.81 | 0.718 | 0.916 | 1.000 | 4227 | tags=60%, list=21%, signal=75% | |
2558 | SELENIUM COMPOUND METABOLIC PROCESS | 101 | -0.22 | -0.81 | 0.606 | 0.916 | 1.000 | 9766 | tags=58%, list=47%, signal=110% | |
2559 | SULFUR COMPOUND BIOSYNTHETIC PROCESS | 138 | -0.20 | -0.81 | 0.803 | 0.916 | 1.000 | 4393 | tags=25%, list=21%, signal=31% | |
2560 | MONOCYTE DIFFERENTIATION | 16 | -0.29 | -0.81 | 0.767 | 0.916 | 1.000 | 5420 | tags=44%, list=26%, signal=59% | |
2561 | REGULATION OF HAIR CYCLE | 10 | -0.33 | -0.81 | 0.693 | 0.916 | 1.000 | 1494 | tags=20%, list=7%, signal=22% | |
2562 | PURINE DEOXYRIBONUCLEOTIDE METABOLIC PROCESS | 9 | -0.38 | -0.81 | 0.698 | 0.916 | 1.000 | 2575 | tags=22%, list=12%, signal=25% | |
2563 | MEMORY | 23 | -0.25 | -0.81 | 0.750 | 0.915 | 1.000 | 7096 | tags=43%, list=34%, signal=66% | |
2564 | ORGANONITROGEN COMPOUND CATABOLIC PROCESS | 230 | -0.19 | -0.81 | 0.810 | 0.916 | 1.000 | 3258 | tags=19%, list=16%, signal=22% | |
2565 | POSITIVE REGULATION OF CALCINEURIN-NFAT SIGNALING CASCADE | 5 | -0.39 | -0.81 | 0.735 | 0.916 | 1.000 | 6254 | tags=60%, list=30%, signal=86% | |
2566 | RAS PROTEIN SIGNAL TRANSDUCTION | 261 | -0.17 | -0.81 | 0.827 | 0.916 | 1.000 | 4835 | tags=22%, list=23%, signal=29% | |
2567 | STRIATUM DEVELOPMENT | 15 | -0.27 | -0.80 | 0.728 | 0.917 | 1.000 | 4733 | tags=33%, list=23%, signal=43% | |
2568 | REGULATION OF INTERLEUKIN-4 PRODUCTION | 14 | -0.29 | -0.80 | 0.770 | 0.917 | 1.000 | 4557 | tags=36%, list=22%, signal=46% | |
2569 | MICROTUBULE POLYMERIZATION | 15 | -0.29 | -0.80 | 0.730 | 0.916 | 1.000 | 4787 | tags=27%, list=23%, signal=35% | |
2570 | REGULATION OF FATTY ACID BETA-OXIDATION | 8 | -0.35 | -0.80 | 0.698 | 0.917 | 1.000 | 186 | tags=13%, list=1%, signal=13% | |
2571 | POSITIVE REGULATION OF ALPHA-BETA T CELL DIFFERENTIATION | 20 | -0.25 | -0.80 | 0.774 | 0.919 | 1.000 | 5601 | tags=40%, list=27%, signal=55% | |
2572 | STRIATED MUSCLE CONTRACTION | 60 | -0.23 | -0.80 | 0.753 | 0.919 | 1.000 | 4131 | tags=25%, list=20%, signal=31% | |
2573 | DICARBOXYLIC ACID METABOLIC PROCESS | 48 | -0.23 | -0.80 | 0.778 | 0.919 | 1.000 | 3861 | tags=25%, list=19%, signal=31% | |
2574 | AORTA DEVELOPMENT | 42 | -0.23 | -0.80 | 0.784 | 0.919 | 1.000 | 3849 | tags=26%, list=19%, signal=32% | |
2575 | REGULATION OF NEUROLOGICAL SYSTEM PROCESS | 16 | -0.28 | -0.80 | 0.754 | 0.919 | 1.000 | 796 | tags=13%, list=4%, signal=13% | |
2576 | POSITIVE REGULATION OF RIG-I SIGNALING PATHWAY | 5 | -0.40 | -0.80 | 0.669 | 0.919 | 1.000 | 3880 | tags=20%, list=19%, signal=25% | |
2577 | TELOMERE MAINTENANCE IN RESPONSE TO DNA DAMAGE | 5 | -0.40 | -0.80 | 0.718 | 0.920 | 1.000 | 5439 | tags=40%, list=26%, signal=54% | |
2578 | PEPTIDYL-PROLINE MODIFICATION | 15 | -0.29 | -0.80 | 0.757 | 0.920 | 1.000 | 5358 | tags=40%, list=26%, signal=54% | |
2579 | SENSORY PERCEPTION OF TASTE | 29 | -0.28 | -0.80 | 0.691 | 0.920 | 1.000 | 4184 | tags=31%, list=20%, signal=39% | |
2580 | REGULATION OF LYMPHOCYTE PROLIFERATION | 105 | -0.19 | -0.80 | 0.817 | 0.919 | 1.000 | 3350 | tags=19%, list=16%, signal=23% | |
2581 | RESPONSE TO ORGANIC CYCLIC COMPOUND | 247 | -0.17 | -0.80 | 0.910 | 0.919 | 1.000 | 4914 | tags=23%, list=24%, signal=29% | |
2582 | MODIFICATION BY HOST OF SYMBIONT MORPHOLOGY OR PHYSIOLOGY | 39 | -0.23 | -0.80 | 0.791 | 0.919 | 1.000 | 4909 | tags=26%, list=24%, signal=34% | |
2583 | PEPTIDYL-ARGININE N-METHYLATION | 8 | -0.35 | -0.80 | 0.718 | 0.919 | 1.000 | 3006 | tags=25%, list=15%, signal=29% | |
2584 | NEGATIVE REGULATION OF SECRETION | 87 | -0.22 | -0.80 | 0.778 | 0.918 | 1.000 | 4445 | tags=28%, list=22%, signal=35% | |
2585 | STEM CELL DEVELOPMENT | 110 | -0.19 | -0.80 | 0.825 | 0.918 | 1.000 | 7039 | tags=37%, list=34%, signal=56% | |
2586 | POSITIVE REGULATION OF PROTEIN TARGETING TO MITOCHONDRION | 72 | -0.20 | -0.80 | 0.780 | 0.918 | 1.000 | 6160 | tags=32%, list=30%, signal=45% | |
2587 | CARBOHYDRATE TRANSPORT | 62 | -0.20 | -0.80 | 0.832 | 0.918 | 1.000 | 1607 | tags=13%, list=8%, signal=14% | |
2588 | INTERACTION WITH SYMBIONT | 40 | -0.23 | -0.80 | 0.787 | 0.918 | 1.000 | 4909 | tags=25%, list=24%, signal=33% | |
2589 | ALPHA-AMINO ACID METABOLIC PROCESS | 228 | -0.16 | -0.80 | 0.823 | 0.918 | 1.000 | 7441 | tags=34%, list=36%, signal=53% | |
2590 | NEGATIVE REGULATION OF TRANSLATIONAL INITIATION | 14 | -0.31 | -0.80 | 0.715 | 0.918 | 1.000 | 2385 | tags=21%, list=12%, signal=24% | |
2591 | MICROTUBULE DEPOLYMERIZATION | 6 | -0.42 | -0.80 | 0.698 | 0.918 | 1.000 | 7859 | tags=50%, list=38%, signal=81% | |
2592 | RESPONSE TO REACTIVE OXYGEN SPECIES | 88 | -0.21 | -0.80 | 0.834 | 0.919 | 1.000 | 3090 | tags=17%, list=15%, signal=20% | |
2593 | REGENERATION | 46 | -0.22 | -0.80 | 0.791 | 0.918 | 1.000 | 6581 | tags=35%, list=32%, signal=51% | |
2594 | MAMMARY GLAND EPITHELIAL CELL PROLIFERATION | 13 | -0.30 | -0.80 | 0.708 | 0.919 | 1.000 | 7178 | tags=46%, list=35%, signal=71% | |
2595 | REGULATION OF GENE EXPRESSION BY GENETIC IMPRINTING | 6 | -0.37 | -0.80 | 0.702 | 0.919 | 1.000 | 7448 | tags=50%, list=36%, signal=78% | |
2596 | GENETIC IMPRINTING | 6 | -0.37 | -0.80 | 0.702 | 0.918 | 1.000 | 7448 | tags=50%, list=36%, signal=78% | |
2597 | POSITIVE REGULATION OF NATURAL KILLER CELL ACTIVATION | 9 | -0.29 | -0.80 | 0.751 | 0.918 | 1.000 | 1014 | tags=11%, list=5%, signal=12% | |
2598 | NEGATIVE REGULATION OF SEQUESTERING OF TRIGLYCERIDE | 5 | -0.39 | -0.80 | 0.729 | 0.919 | 1.000 | 2933 | tags=40%, list=14%, signal=47% | |
2599 | T CELL MEDIATED IMMUNITY | 13 | -0.31 | -0.80 | 0.741 | 0.919 | 1.000 | 935 | tags=15%, list=5%, signal=16% | |
2600 | PEPTIDYL-ARGININE METHYLATION | 9 | -0.33 | -0.80 | 0.744 | 0.919 | 1.000 | 3006 | tags=22%, list=15%, signal=26% | |
2601 | METHYLATION | 118 | -0.20 | -0.80 | 0.778 | 0.919 | 1.000 | 3839 | tags=19%, list=19%, signal=24% | |
2602 | DRUG TRANSPORT | 14 | -0.29 | -0.80 | 0.759 | 0.919 | 1.000 | 6597 | tags=50%, list=32%, signal=73% | |
2603 | BLOOD VESSEL ENDOTHELIAL CELL DIFFERENTIATION | 7 | -0.36 | -0.80 | 0.700 | 0.919 | 1.000 | 1322 | tags=14%, list=6%, signal=15% | |
2604 | POSITIVE REGULATION OF LEUKOCYTE PROLIFERATION | 73 | -0.20 | -0.80 | 0.832 | 0.919 | 1.000 | 3350 | tags=19%, list=16%, signal=23% | |
2605 | PROTEIN PEPTIDYL-PROLYL ISOMERIZATION | 10 | -0.33 | -0.80 | 0.731 | 0.920 | 1.000 | 5358 | tags=50%, list=26%, signal=68% | |
2606 | REGULATION OF RESPIRATORY BURST | 9 | -0.35 | -0.79 | 0.709 | 0.920 | 1.000 | 4162 | tags=44%, list=20%, signal=56% | |
2607 | POSITIVE REGULATION OF TRIGLYCERIDE LIPASE ACTIVITY | 7 | -0.37 | -0.79 | 0.720 | 0.920 | 1.000 | 4193 | tags=43%, list=20%, signal=54% | |
2608 | RESPONSE TO OSMOTIC STRESS | 22 | -0.25 | -0.79 | 0.802 | 0.921 | 1.000 | 5399 | tags=32%, list=26%, signal=43% | |
2609 | RRNA TRANSCRIPTION | 7 | -0.38 | -0.79 | 0.731 | 0.922 | 1.000 | 8135 | tags=71%, list=39%, signal=118% | |
2610 | CHROMOSOME SEPARATION | 5 | -0.40 | -0.79 | 0.753 | 0.922 | 1.000 | 557 | tags=20%, list=3%, signal=21% | |
2611 | GLUTAMINE FAMILY AMINO ACID CATABOLIC PROCESS | 14 | -0.30 | -0.79 | 0.746 | 0.922 | 1.000 | 6854 | tags=43%, list=33%, signal=64% | |
2612 | MORPHOGENESIS OF AN EPITHELIAL FOLD | 19 | -0.26 | -0.79 | 0.718 | 0.922 | 1.000 | 4914 | tags=42%, list=24%, signal=55% | |
2613 | TRACHEA CARTILAGE DEVELOPMENT | 7 | -0.36 | -0.79 | 0.704 | 0.923 | 1.000 | 1985 | tags=29%, list=10%, signal=32% | |
2614 | LYMPHOCYTE COSTIMULATION | 59 | -0.22 | -0.79 | 0.802 | 0.923 | 1.000 | 2133 | tags=17%, list=10%, signal=19% | |
2615 | T CELL COSTIMULATION | 59 | -0.22 | -0.79 | 0.802 | 0.923 | 1.000 | 2133 | tags=17%, list=10%, signal=19% | |
2616 | EMBRYONIC PLACENTA MORPHOGENESIS | 27 | -0.24 | -0.79 | 0.795 | 0.923 | 1.000 | 2211 | tags=15%, list=11%, signal=17% | |
2617 | NEGATIVE REGULATION OF SECRETION BY CELL | 80 | -0.21 | -0.79 | 0.758 | 0.923 | 1.000 | 4445 | tags=28%, list=22%, signal=35% | |
2618 | REGULATION OF OSSIFICATION | 77 | -0.19 | -0.79 | 0.857 | 0.923 | 1.000 | 5465 | tags=26%, list=27%, signal=35% | |
2619 | MONOVALENT INORGANIC ANION HOMEOSTASIS | 12 | -0.30 | -0.79 | 0.705 | 0.923 | 1.000 | 7087 | tags=50%, list=34%, signal=76% | |
2620 | NEGATIVE REGULATION OF DEPHOSPHORYLATION | 47 | -0.21 | -0.79 | 0.816 | 0.923 | 1.000 | 2053 | tags=15%, list=10%, signal=17% | |
2621 | NEGATIVE REGULATION OF PROTEIN DEPHOSPHORYLATION | 47 | -0.21 | -0.79 | 0.816 | 0.923 | 1.000 | 2053 | tags=15%, list=10%, signal=17% | |
2622 | POSITIVE REGULATION OF GLYCOPROTEIN BIOSYNTHETIC PROCESS | 11 | -0.30 | -0.79 | 0.734 | 0.922 | 1.000 | 5601 | tags=45%, list=27%, signal=62% | |
2623 | RESPONSE TO FLUID SHEAR STRESS | 19 | -0.27 | -0.79 | 0.746 | 0.925 | 1.000 | 1637 | tags=16%, list=8%, signal=17% | |
2624 | HEART GROWTH | 18 | -0.28 | -0.79 | 0.759 | 0.925 | 1.000 | 395 | tags=11%, list=2%, signal=11% | |
2625 | REGULATION OF MONONUCLEAR CELL PROLIFERATION | 106 | -0.19 | -0.79 | 0.840 | 0.925 | 1.000 | 3350 | tags=19%, list=16%, signal=22% | |
2626 | PARTURITION | 5 | -0.39 | -0.79 | 0.739 | 0.925 | 1.000 | 815 | tags=20%, list=4%, signal=21% | |
2627 | CELL COMMUNICATION INVOLVED IN CARDIAC CONDUCTION | 32 | -0.25 | -0.79 | 0.758 | 0.925 | 1.000 | 5637 | tags=41%, list=27%, signal=56% | |
2628 | POSITIVE REGULATION OF DNA METABOLIC PROCESS | 115 | -0.21 | -0.79 | 0.789 | 0.925 | 1.000 | 5650 | tags=33%, list=27%, signal=45% | |
2629 | CARBOHYDRATE DERIVATIVE CATABOLIC PROCESS | 127 | -0.20 | -0.79 | 0.805 | 0.925 | 1.000 | 3258 | tags=19%, list=16%, signal=22% | |
2630 | RETINA LAYER FORMATION | 21 | -0.25 | -0.79 | 0.794 | 0.925 | 1.000 | 9206 | tags=52%, list=45%, signal=95% | |
2631 | GLUCURONATE CATABOLIC PROCESS | 5 | -0.40 | -0.79 | 0.720 | 0.925 | 1.000 | 1643 | tags=20%, list=8%, signal=22% | |
2632 | GLUCURONATE CATABOLIC PROCESS TO XYLULOSE 5-PHOSPHATE | 5 | -0.40 | -0.79 | 0.720 | 0.925 | 1.000 | 1643 | tags=20%, list=8%, signal=22% | |
2633 | XYLULOSE 5-PHOSPHATE METABOLIC PROCESS | 5 | -0.40 | -0.79 | 0.720 | 0.924 | 1.000 | 1643 | tags=20%, list=8%, signal=22% | |
2634 | XYLULOSE 5-PHOSPHATE BIOSYNTHETIC PROCESS | 5 | -0.40 | -0.79 | 0.720 | 0.924 | 1.000 | 1643 | tags=20%, list=8%, signal=22% | |
2635 | PROTEIN OLIGOMERIZATION | 193 | -0.18 | -0.79 | 0.870 | 0.924 | 1.000 | 5586 | tags=30%, list=27%, signal=40% | |
2636 | REGULATION OF HORMONE BIOSYNTHETIC PROCESS | 10 | -0.32 | -0.79 | 0.751 | 0.925 | 1.000 | 5050 | tags=40%, list=25%, signal=53% | |
2637 | REGULATION OF TYPE B PANCREATIC CELL APOPTOTIC PROCESS | 5 | -0.39 | -0.79 | 0.740 | 0.925 | 1.000 | 1277 | tags=20%, list=6%, signal=21% | |
2638 | NEGATIVE REGULATION OF BETA-AMYLOID FORMATION | 5 | -0.40 | -0.79 | 0.749 | 0.925 | 1.000 | 9743 | tags=80%, list=47%, signal=152% | |
2639 | REGULATION OF COLLAGEN BIOSYNTHETIC PROCESS | 11 | -0.31 | -0.79 | 0.751 | 0.925 | 1.000 | 7097 | tags=55%, list=34%, signal=83% | |
2640 | NEGATIVE REGULATION OF STEROID BIOSYNTHETIC PROCESS | 15 | -0.28 | -0.79 | 0.751 | 0.925 | 1.000 | 5050 | tags=33%, list=25%, signal=44% | |
2641 | NEGATIVE REGULATION OF STEROID METABOLIC PROCESS | 15 | -0.28 | -0.79 | 0.751 | 0.925 | 1.000 | 5050 | tags=33%, list=25%, signal=44% | |
2642 | ESTABLISHMENT OR MAINTENANCE OF APICAL/BASAL CELL POLARITY | 14 | -0.29 | -0.78 | 0.738 | 0.925 | 1.000 | 6789 | tags=57%, list=33%, signal=85% | |
2643 | ESTABLISHMENT OR MAINTENANCE OF BIPOLAR CELL POLARITY | 14 | -0.29 | -0.78 | 0.738 | 0.925 | 1.000 | 6789 | tags=57%, list=33%, signal=85% | |
2644 | REGULATION OF VENTRICULAR CARDIAC MUSCLE CELL MEMBRANE REPOLARIZATION | 12 | -0.30 | -0.78 | 0.742 | 0.924 | 1.000 | 3843 | tags=25%, list=19%, signal=31% | |
2645 | CARDIAC CELL FATE COMMITMENT | 8 | -0.30 | -0.78 | 0.722 | 0.924 | 1.000 | 6235 | tags=50%, list=30%, signal=72% | |
2646 | REGULATION OF CELLULAR COMPONENT SIZE | 169 | -0.18 | -0.78 | 0.895 | 0.924 | 1.000 | 5317 | tags=26%, list=26%, signal=35% | |
2647 | RESPONSE TO MONOAMINE | 20 | -0.26 | -0.78 | 0.764 | 0.924 | 1.000 | 2509 | tags=15%, list=12%, signal=17% | |
2648 | CELLULAR RESPONSE TO MONOAMINE STIMULUS | 20 | -0.26 | -0.78 | 0.764 | 0.924 | 1.000 | 2509 | tags=15%, list=12%, signal=17% | |
2649 | RESPONSE TO CATECHOLAMINE | 20 | -0.26 | -0.78 | 0.764 | 0.923 | 1.000 | 2509 | tags=15%, list=12%, signal=17% | |
2650 | CELLULAR RESPONSE TO CATECHOLAMINE STIMULUS | 20 | -0.26 | -0.78 | 0.764 | 0.923 | 1.000 | 2509 | tags=15%, list=12%, signal=17% | |
2651 | REGULATION OF T CELL DIFFERENTIATION | 50 | -0.21 | -0.78 | 0.859 | 0.923 | 1.000 | 5743 | tags=34%, list=28%, signal=47% | |
2652 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 11 | -0.32 | -0.78 | 0.729 | 0.923 | 1.000 | 7639 | tags=45%, list=37%, signal=72% | |
2653 | POSITIVE REGULATION OF KINASE ACTIVITY | 440 | -0.17 | -0.78 | 0.896 | 0.923 | 1.000 | 5650 | tags=27%, list=27%, signal=36% | |
2654 | NEGATIVE REGULATION OF DNA BINDING | 28 | -0.24 | -0.78 | 0.827 | 0.922 | 1.000 | 3984 | tags=21%, list=19%, signal=27% | |
2655 | REGULATION OF EXTRACELLULAR MATRIX DISASSEMBLY | 11 | -0.31 | -0.78 | 0.723 | 0.923 | 1.000 | 2689 | tags=27%, list=13%, signal=31% | |
2656 | BODY FLUID SECRETION | 37 | -0.23 | -0.78 | 0.803 | 0.923 | 1.000 | 3815 | tags=24%, list=19%, signal=30% | |
2657 | REGULATION OF CELL PROJECTION ASSEMBLY | 74 | -0.18 | -0.78 | 0.856 | 0.923 | 1.000 | 6604 | tags=36%, list=32%, signal=54% | |
2658 | POSITIVE REGULATION OF LIPOPROTEIN LIPASE ACTIVITY | 6 | -0.38 | -0.78 | 0.736 | 0.923 | 1.000 | 4193 | tags=50%, list=20%, signal=63% | |
2659 | NEUTRAL AMINO ACID TRANSPORT | 19 | -0.29 | -0.78 | 0.755 | 0.923 | 1.000 | 2954 | tags=21%, list=14%, signal=25% | |
2660 | PURINE NUCLEOSIDE DIPHOSPHATE METABOLIC PROCESS | 38 | -0.24 | -0.78 | 0.756 | 0.923 | 1.000 | 2064 | tags=13%, list=10%, signal=15% | |
2661 | PURINE RIBONUCLEOSIDE DIPHOSPHATE METABOLIC PROCESS | 38 | -0.24 | -0.78 | 0.756 | 0.922 | 1.000 | 2064 | tags=13%, list=10%, signal=15% | |
2662 | SPERM CAPACITATION | 13 | -0.27 | -0.78 | 0.787 | 0.922 | 1.000 | 4139 | tags=23%, list=20%, signal=29% | |
2663 | SYNAPTIC VESICLE RECYCLING | 12 | -0.31 | -0.78 | 0.743 | 0.923 | 1.000 | 6876 | tags=58%, list=33%, signal=87% | |
2664 | ACTIN FILAMENT-BASED PROCESS | 276 | -0.17 | -0.78 | 0.899 | 0.923 | 1.000 | 4913 | tags=23%, list=24%, signal=30% | |
2665 | CELLULAR RESPONSE TO DRUG | 29 | -0.23 | -0.78 | 0.786 | 0.922 | 1.000 | 4909 | tags=31%, list=24%, signal=41% | |
2666 | HEPARAN SULFATE PROTEOGLYCAN METABOLIC PROCESS | 11 | -0.29 | -0.78 | 0.759 | 0.923 | 1.000 | 3927 | tags=36%, list=19%, signal=45% | |
2667 | SPHINGOLIPID BIOSYNTHETIC PROCESS | 34 | -0.22 | -0.78 | 0.776 | 0.924 | 1.000 | 2090 | tags=15%, list=10%, signal=16% | |
2668 | NEGATIVE REGULATION OF PROTEIN EXPORT FROM NUCLEUS | 5 | -0.39 | -0.78 | 0.757 | 0.924 | 1.000 | 3533 | tags=40%, list=17%, signal=48% | |
2669 | REGULATION OF ATPASE ACTIVITY | 39 | -0.22 | -0.78 | 0.817 | 0.924 | 1.000 | 4979 | tags=31%, list=24%, signal=40% | |
2670 | SOMITE ROSTRAL/CAUDAL AXIS SPECIFICATION | 8 | -0.32 | -0.78 | 0.735 | 0.925 | 1.000 | 485 | tags=13%, list=2%, signal=13% | |
2671 | POSITIVE REGULATION OF INSULIN SECRETION INVOLVED IN CELLULAR RESPONSE TO GLUCOSE STIMULUS | 6 | -0.35 | -0.78 | 0.705 | 0.924 | 1.000 | 6278 | tags=50%, list=30%, signal=72% | |
2672 | POSITIVE REGULATION OF TRANSPORTER ACTIVITY | 43 | -0.21 | -0.78 | 0.778 | 0.926 | 1.000 | 6561 | tags=35%, list=32%, signal=51% | |
2673 | REGULATION OF MEMBRANE REPOLARIZATION | 23 | -0.25 | -0.78 | 0.784 | 0.925 | 1.000 | 5637 | tags=39%, list=27%, signal=54% | |
2674 | MYOBLAST MIGRATION | 6 | -0.37 | -0.78 | 0.756 | 0.926 | 1.000 | 3105 | tags=33%, list=15%, signal=39% | |
2675 | NEGATIVE REGULATION OF INTERLEUKIN-10 PRODUCTION | 12 | -0.30 | -0.78 | 0.787 | 0.927 | 1.000 | 2592 | tags=25%, list=13%, signal=29% | |
2676 | SIGNAL TRANSDUCTION BY PROTEIN PHOSPHORYLATION | 306 | -0.17 | -0.78 | 0.893 | 0.928 | 1.000 | 4219 | tags=20%, list=20%, signal=25% | |
2677 | POSITIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA PRODUCTION | 8 | -0.37 | -0.78 | 0.753 | 0.928 | 1.000 | 7208 | tags=63%, list=35%, signal=96% | |
2678 | RESPONSE TO TOPOLOGICALLY INCORRECT PROTEIN | 116 | -0.21 | -0.78 | 0.791 | 0.928 | 1.000 | 4323 | tags=23%, list=21%, signal=29% | |
2679 | RESPONSE TO ORGANONITROGEN COMPOUND | 485 | -0.16 | -0.78 | 0.968 | 0.928 | 1.000 | 4902 | tags=23%, list=24%, signal=29% | |
2680 | OXIDATIVE PHOSPHORYLATION | 8 | -0.36 | -0.78 | 0.716 | 0.928 | 1.000 | 536 | tags=13%, list=3%, signal=13% | |
2681 | MAPK CASCADE | 296 | -0.17 | -0.78 | 0.902 | 0.928 | 1.000 | 3191 | tags=16%, list=15%, signal=19% | |
2682 | REGULATION OF ACROSOME REACTION | 5 | -0.37 | -0.78 | 0.775 | 0.928 | 1.000 | 2372 | tags=40%, list=12%, signal=45% | |
2683 | POSITIVE REGULATION OF ACROSOME REACTION | 5 | -0.37 | -0.78 | 0.775 | 0.927 | 1.000 | 2372 | tags=40%, list=12%, signal=45% | |
2684 | NEURON PROJECTION REGENERATION | 16 | -0.29 | -0.78 | 0.729 | 0.927 | 1.000 | 3984 | tags=25%, list=19%, signal=31% | |
2685 | FAT CELL DIFFERENTIATION | 94 | -0.20 | -0.77 | 0.865 | 0.927 | 1.000 | 4093 | tags=21%, list=20%, signal=26% | |
2686 | FRUCTOSE METABOLIC PROCESS | 8 | -0.35 | -0.77 | 0.746 | 0.927 | 1.000 | 3819 | tags=25%, list=19%, signal=31% | |
2687 | NUCLEOSIDE PHOSPHATE METABOLIC PROCESS | 244 | -0.18 | -0.77 | 0.878 | 0.927 | 1.000 | 2946 | tags=15%, list=14%, signal=17% | |
2688 | NORADRENERGIC NEURON DIFFERENTIATION | 6 | -0.35 | -0.77 | 0.758 | 0.927 | 1.000 | 2052 | tags=17%, list=10%, signal=19% | |
2689 | NEGATIVE REGULATION OF ION TRANSPORT | 67 | -0.20 | -0.77 | 0.847 | 0.927 | 1.000 | 4352 | tags=22%, list=21%, signal=28% | |
2690 | NATURAL KILLER CELL MEDIATED CYTOTOXICITY | 10 | -0.31 | -0.77 | 0.728 | 0.926 | 1.000 | 1595 | tags=20%, list=8%, signal=22% | |
2691 | REGULATION OF MEMBRANE POTENTIAL | 165 | -0.18 | -0.77 | 0.858 | 0.926 | 1.000 | 6120 | tags=30%, list=30%, signal=43% | |
2692 | EMBRYONIC PROCESS INVOLVED IN FEMALE PREGNANCY | 7 | -0.39 | -0.77 | 0.746 | 0.926 | 1.000 | 3677 | tags=57%, list=18%, signal=70% | |
2693 | 'DE NOVO' POSTTRANSLATIONAL PROTEIN FOLDING | 30 | -0.27 | -0.77 | 0.708 | 0.926 | 1.000 | 3382 | tags=17%, list=16%, signal=20% | |
2694 | RECEPTOR-MEDIATED ENDOCYTOSIS | 135 | -0.20 | -0.77 | 0.835 | 0.927 | 1.000 | 3563 | tags=19%, list=17%, signal=23% | |
2695 | FIBRIL ORGANIZATION | 15 | -0.30 | -0.77 | 0.729 | 0.927 | 1.000 | 1877 | tags=20%, list=9%, signal=22% | |
2696 | REGULATION OF HETEROTYPIC CELL-CELL ADHESION | 16 | -0.28 | -0.77 | 0.801 | 0.926 | 1.000 | 1637 | tags=19%, list=8%, signal=20% | |
2697 | ACTIVATION OF MAPKK ACTIVITY | 206 | -0.17 | -0.77 | 0.895 | 0.926 | 1.000 | 1609 | tags=10%, list=8%, signal=11% | |
2698 | CARDIAC CHAMBER FORMATION | 11 | -0.30 | -0.77 | 0.736 | 0.926 | 1.000 | 4163 | tags=27%, list=20%, signal=34% | |
2699 | REGULATION OF PROTEIN ACETYLATION | 37 | -0.22 | -0.77 | 0.817 | 0.926 | 1.000 | 5743 | tags=35%, list=28%, signal=49% | |
2700 | POSITIVE REGULATION OF T CELL APOPTOTIC PROCESS | 7 | -0.34 | -0.77 | 0.779 | 0.927 | 1.000 | 2133 | tags=14%, list=10%, signal=16% | |
2701 | ACTIVATION OF PROTEIN KINASE ACTIVITY | 347 | -0.17 | -0.77 | 0.931 | 0.927 | 1.000 | 4902 | tags=23%, list=24%, signal=30% | |
2702 | PURINE RIBONUCLEOTIDE CATABOLIC PROCESS | 16 | -0.27 | -0.77 | 0.775 | 0.927 | 1.000 | 793 | tags=13%, list=4%, signal=13% | |
2703 | LENS INDUCTION IN CAMERA-TYPE EYE | 7 | -0.34 | -0.77 | 0.763 | 0.927 | 1.000 | 5056 | tags=29%, list=25%, signal=38% | |
2704 | REGULATION OF MAP KINASE ACTIVITY | 348 | -0.17 | -0.77 | 0.917 | 0.927 | 1.000 | 5650 | tags=26%, list=27%, signal=35% | |
2705 | SOMATOTROPIN SECRETING CELL DIFFERENTIATION | 5 | -0.38 | -0.77 | 0.729 | 0.927 | 1.000 | 6352 | tags=40%, list=31%, signal=58% | |
2706 | POSITIVE REGULATION OF MONOOXYGENASE ACTIVITY | 20 | -0.26 | -0.77 | 0.757 | 0.927 | 1.000 | 837 | tags=10%, list=4%, signal=10% | |
2707 | XENOBIOTIC METABOLIC PROCESS | 162 | -0.18 | -0.77 | 0.923 | 0.927 | 1.000 | 6077 | tags=32%, list=29%, signal=45% | |
2708 | REGULATION OF INTERFERON-GAMMA BIOSYNTHETIC PROCESS | 13 | -0.29 | -0.77 | 0.755 | 0.927 | 1.000 | 913 | tags=15%, list=4%, signal=16% | |
2709 | REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 37 | -0.24 | -0.77 | 0.811 | 0.927 | 1.000 | 6354 | tags=38%, list=31%, signal=55% | |
2710 | RRNA METABOLIC PROCESS | 44 | -0.27 | -0.77 | 0.706 | 0.928 | 1.000 | 9224 | tags=57%, list=45%, signal=103% | |
2711 | NUCLEOSIDE BISPHOSPHATE METABOLIC PROCESS | 26 | -0.24 | -0.77 | 0.798 | 0.927 | 1.000 | 6781 | tags=46%, list=33%, signal=69% | |
2712 | RIBONUCLEOSIDE BISPHOSPHATE METABOLIC PROCESS | 26 | -0.24 | -0.77 | 0.798 | 0.927 | 1.000 | 6781 | tags=46%, list=33%, signal=69% | |
2713 | PURINE NUCLEOSIDE BISPHOSPHATE METABOLIC PROCESS | 26 | -0.24 | -0.77 | 0.798 | 0.926 | 1.000 | 6781 | tags=46%, list=33%, signal=69% | |
2714 | NEUROEPITHELIAL CELL DIFFERENTIATION | 63 | -0.20 | -0.77 | 0.836 | 0.926 | 1.000 | 6073 | tags=38%, list=29%, signal=54% | |
2715 | REGULATION OF STRIATED MUSCLE CONTRACTION | 59 | -0.21 | -0.77 | 0.809 | 0.926 | 1.000 | 5630 | tags=34%, list=27%, signal=47% | |
2716 | NEGATIVE REGULATION OF CYCLASE ACTIVITY | 17 | -0.26 | -0.77 | 0.777 | 0.927 | 1.000 | 3494 | tags=29%, list=17%, signal=35% | |
2717 | NEGATIVE REGULATION OF METANEPHROS DEVELOPMENT | 6 | -0.36 | -0.77 | 0.758 | 0.927 | 1.000 | 1797 | tags=33%, list=9%, signal=37% | |
2718 | DETECTION OF CHEMICAL STIMULUS INVOLVED IN SENSORY PERCEPTION OF BITTER TASTE | 24 | -0.27 | -0.77 | 0.733 | 0.927 | 1.000 | 4184 | tags=29%, list=20%, signal=37% | |
2719 | SENSORY PERCEPTION OF BITTER TASTE | 24 | -0.27 | -0.77 | 0.733 | 0.926 | 1.000 | 4184 | tags=29%, list=20%, signal=37% | |
2720 | HETEROPHILIC CELL-CELL ADHESION VIA PLASMA MEMBRANE CELL ADHESION MOLECULES | 23 | -0.23 | -0.77 | 0.782 | 0.926 | 1.000 | 2971 | tags=17%, list=14%, signal=20% | |
2721 | OMEGA-HYDROXYLASE P450 PATHWAY | 9 | -0.31 | -0.77 | 0.761 | 0.927 | 1.000 | 5590 | tags=44%, list=27%, signal=61% | |
2722 | MUSCLE CELL MIGRATION | 12 | -0.29 | -0.77 | 0.786 | 0.927 | 1.000 | 3849 | tags=33%, list=19%, signal=41% | |
2723 | CELL-CELL SIGNALING INVOLVED IN CARDIAC CONDUCTION | 15 | -0.30 | -0.77 | 0.740 | 0.927 | 1.000 | 5637 | tags=40%, list=27%, signal=55% | |
2724 | RESPONSE TO XENOBIOTIC STIMULUS | 163 | -0.18 | -0.77 | 0.938 | 0.926 | 1.000 | 6077 | tags=32%, list=29%, signal=45% | |
2725 | CELLULAR RESPONSE TO XENOBIOTIC STIMULUS | 163 | -0.18 | -0.77 | 0.938 | 0.926 | 1.000 | 6077 | tags=32%, list=29%, signal=45% | |
2726 | SMALL MOLECULE BIOSYNTHETIC PROCESS | 251 | -0.18 | -0.77 | 0.892 | 0.926 | 1.000 | 4538 | tags=21%, list=22%, signal=27% | |
2727 | CELLULAR KETONE METABOLIC PROCESS | 39 | -0.23 | -0.77 | 0.763 | 0.926 | 1.000 | 3533 | tags=21%, list=17%, signal=25% | |
2728 | LEUKOCYTE CELL-CELL ADHESION | 201 | -0.18 | -0.77 | 0.899 | 0.926 | 1.000 | 4016 | tags=20%, list=19%, signal=24% | |
2729 | REGULATION OF SYNAPSE ASSEMBLY | 21 | -0.26 | -0.77 | 0.737 | 0.926 | 1.000 | 2259 | tags=19%, list=11%, signal=21% | |
2730 | SPLICEOSOMAL TRI-SNRNP COMPLEX ASSEMBLY | 8 | -0.34 | -0.77 | 0.717 | 0.926 | 1.000 | 4532 | tags=25%, list=22%, signal=32% | |
2731 | TYPE II PNEUMOCYTE DIFFERENTIATION | 5 | -0.38 | -0.77 | 0.750 | 0.926 | 1.000 | 3815 | tags=40%, list=19%, signal=49% | |
2732 | PLATELET AGGREGATION | 30 | -0.24 | -0.77 | 0.767 | 0.926 | 1.000 | 5285 | tags=30%, list=26%, signal=40% | |
2733 | PARAXIAL MESODERM MORPHOGENESIS | 10 | -0.28 | -0.77 | 0.795 | 0.925 | 1.000 | 6710 | tags=40%, list=33%, signal=59% | |
2734 | POSITIVE REGULATION OF PROTEIN SERINE/THREONINE KINASE ACTIVITY | 176 | -0.18 | -0.77 | 0.864 | 0.925 | 1.000 | 5650 | tags=27%, list=27%, signal=37% | |
2735 | DEVELOPMENTAL PROGRAMMED CELL DEATH | 27 | -0.23 | -0.77 | 0.835 | 0.925 | 1.000 | 946 | tags=11%, list=5%, signal=12% | |
2736 | STRIATED MUSCLE HYPERTROPHY | 11 | -0.29 | -0.76 | 0.766 | 0.926 | 1.000 | 5630 | tags=45%, list=27%, signal=63% | |
2737 | MODULATION BY HOST OF VIRAL PROCESS | 16 | -0.27 | -0.76 | 0.786 | 0.926 | 1.000 | 4307 | tags=25%, list=21%, signal=32% | |
2738 | RIBONUCLEOTIDE CATABOLIC PROCESS | 17 | -0.26 | -0.76 | 0.789 | 0.927 | 1.000 | 793 | tags=12%, list=4%, signal=12% | |
2739 | NEGATIVE REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 10 | -0.31 | -0.76 | 0.774 | 0.926 | 1.000 | 4163 | tags=30%, list=20%, signal=38% | |
2740 | PEPTIDE CROSS-LINKING | 13 | -0.29 | -0.76 | 0.791 | 0.927 | 1.000 | 4374 | tags=46%, list=21%, signal=59% | |
2741 | POLYAMINE BIOSYNTHETIC PROCESS | 5 | -0.38 | -0.76 | 0.769 | 0.926 | 1.000 | 5852 | tags=40%, list=28%, signal=56% | |
2742 | NEGATIVE REGULATION OF INTERLEUKIN-1 BETA PRODUCTION | 6 | -0.37 | -0.76 | 0.761 | 0.926 | 1.000 | 444 | tags=17%, list=2%, signal=17% | |
2743 | POSITIVE REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 22 | -0.27 | -0.76 | 0.777 | 0.926 | 1.000 | 6354 | tags=45%, list=31%, signal=66% | |
2744 | BLOOD VESSEL ENDOTHELIAL CELL PROLIFERATION INVOLVED IN SPROUTING ANGIOGENESIS | 6 | -0.36 | -0.76 | 0.754 | 0.926 | 1.000 | 2879 | tags=33%, list=14%, signal=39% | |
2745 | POSITIVE REGULATION OF STRIATED MUSCLE CONTRACTION | 7 | -0.35 | -0.76 | 0.770 | 0.926 | 1.000 | 5243 | tags=43%, list=25%, signal=57% | |
2746 | NEGATIVE REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 25 | -0.24 | -0.76 | 0.835 | 0.926 | 1.000 | 3560 | tags=20%, list=17%, signal=24% | |
2747 | CEREBELLAR PURKINJE CELL LAYER DEVELOPMENT | 27 | -0.23 | -0.76 | 0.804 | 0.926 | 1.000 | 8303 | tags=48%, list=40%, signal=81% | |
2748 | NEGATIVE REGULATION OF CALCIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 19 | -0.25 | -0.76 | 0.818 | 0.926 | 1.000 | 3494 | tags=16%, list=17%, signal=19% | |
2749 | NEGATIVE REGULATION OF CALCIUM ION TRANSMEMBRANE TRANSPORT | 19 | -0.25 | -0.76 | 0.818 | 0.926 | 1.000 | 3494 | tags=16%, list=17%, signal=19% | |
2750 | VENTRICULAR SYSTEM DEVELOPMENT | 26 | -0.23 | -0.76 | 0.804 | 0.926 | 1.000 | 7364 | tags=46%, list=36%, signal=72% | |
2751 | INNER EAR RECEPTOR CELL DIFFERENTIATION | 59 | -0.20 | -0.76 | 0.847 | 0.927 | 1.000 | 6073 | tags=36%, list=29%, signal=50% | |
2752 | CARDIAC VENTRICLE FORMATION | 10 | -0.30 | -0.76 | 0.737 | 0.927 | 1.000 | 4163 | tags=30%, list=20%, signal=38% | |
2753 | ADENOHYPOPHYSIS DEVELOPMENT | 14 | -0.30 | -0.76 | 0.703 | 0.927 | 1.000 | 8407 | tags=43%, list=41%, signal=72% | |
2754 | POSITIVE REGULATION OF CELL-MATRIX ADHESION | 27 | -0.22 | -0.76 | 0.850 | 0.927 | 1.000 | 8841 | tags=59%, list=43%, signal=104% | |
2755 | AUDITORY RECEPTOR CELL FATE COMMITMENT | 5 | -0.39 | -0.76 | 0.777 | 0.928 | 1.000 | 4982 | tags=40%, list=24%, signal=53% | |
2756 | INNER EAR RECEPTOR CELL FATE COMMITMENT | 5 | -0.39 | -0.76 | 0.777 | 0.927 | 1.000 | 4982 | tags=40%, list=24%, signal=53% | |
2757 | LONG-TERM SYNAPTIC POTENTIATION | 10 | -0.31 | -0.76 | 0.770 | 0.928 | 1.000 | 5972 | tags=60%, list=29%, signal=84% | |
2758 | NEGATIVE REGULATION OF MAP KINASE ACTIVITY | 50 | -0.22 | -0.76 | 0.827 | 0.927 | 1.000 | 3630 | tags=22%, list=18%, signal=27% | |
2759 | MONOCYTE CHEMOTAXIS | 10 | -0.31 | -0.76 | 0.778 | 0.927 | 1.000 | 5854 | tags=40%, list=28%, signal=56% | |
2760 | NEGATIVE REGULATION OF NF-KAPPAB TRANSCRIPTION FACTOR ACTIVITY | 52 | -0.22 | -0.76 | 0.824 | 0.927 | 1.000 | 4951 | tags=27%, list=24%, signal=35% | |
2761 | CELLULAR CARBOHYDRATE BIOSYNTHETIC PROCESS | 30 | -0.22 | -0.76 | 0.774 | 0.927 | 1.000 | 4238 | tags=20%, list=21%, signal=25% | |
2762 | NEGATIVE REGULATION OF LYASE ACTIVITY | 19 | -0.25 | -0.76 | 0.807 | 0.927 | 1.000 | 3494 | tags=26%, list=17%, signal=32% | |
2763 | AORTA MORPHOGENESIS | 21 | -0.27 | -0.76 | 0.798 | 0.927 | 1.000 | 4823 | tags=38%, list=23%, signal=50% | |
2764 | HISTONE ARGININE METHYLATION | 8 | -0.33 | -0.76 | 0.762 | 0.927 | 1.000 | 3006 | tags=25%, list=15%, signal=29% | |
2765 | NEURON REMODELING | 11 | -0.30 | -0.76 | 0.800 | 0.929 | 1.000 | 3110 | tags=27%, list=15%, signal=32% | |
2766 | NEGATIVE REGULATION OF PURINE NUCLEOTIDE METABOLIC PROCESS | 31 | -0.24 | -0.76 | 0.797 | 0.928 | 1.000 | 3494 | tags=26%, list=17%, signal=31% | |
2767 | POSITIVE REGULATION OF CARDIAC MUSCLE CELL DIFFERENTIATION | 7 | -0.32 | -0.76 | 0.780 | 0.929 | 1.000 | 7204 | tags=57%, list=35%, signal=88% | |
2768 | CARNITINE METABOLIC PROCESS | 9 | -0.29 | -0.76 | 0.812 | 0.929 | 1.000 | 6895 | tags=44%, list=33%, signal=67% | |
2769 | DESENSITIZATION OF G-PROTEIN COUPLED RECEPTOR PROTEIN SIGNALING PATHWAY | 8 | -0.34 | -0.76 | 0.786 | 0.928 | 1.000 | 2340 | tags=25%, list=11%, signal=28% | |
2770 | NEGATIVE ADAPTATION OF SIGNALING PATHWAY | 8 | -0.34 | -0.76 | 0.786 | 0.928 | 1.000 | 2340 | tags=25%, list=11%, signal=28% | |
2771 | ADAPTATION OF SIGNALING PATHWAY | 8 | -0.34 | -0.76 | 0.786 | 0.928 | 1.000 | 2340 | tags=25%, list=11%, signal=28% | |
2772 | MESENCHYMAL CELL DIFFERENTIATION | 117 | -0.18 | -0.76 | 0.905 | 0.928 | 1.000 | 7048 | tags=38%, list=34%, signal=57% | |
2773 | POSITIVE REGULATION OF ANTIGEN PROCESSING AND PRESENTATION | 6 | -0.37 | -0.76 | 0.762 | 0.928 | 1.000 | 5601 | tags=50%, list=27%, signal=69% | |
2774 | CHEMOKINE-MEDIATED SIGNALING PATHWAY | 22 | -0.26 | -0.76 | 0.857 | 0.928 | 1.000 | 4047 | tags=32%, list=20%, signal=40% | |
2775 | CULLIN DENEDDYLATION | 9 | -0.35 | -0.76 | 0.761 | 0.927 | 1.000 | 5995 | tags=44%, list=29%, signal=63% | |
2776 | MESENCHYMAL CELL DEVELOPMENT | 105 | -0.18 | -0.76 | 0.893 | 0.927 | 1.000 | 6537 | tags=33%, list=32%, signal=49% | |
2777 | ACTIN FILAMENT CAPPING | 6 | -0.35 | -0.75 | 0.783 | 0.927 | 1.000 | 769 | tags=17%, list=4%, signal=17% | |
2778 | NEGATIVE REGULATION OF INTERLEUKIN-1 PRODUCTION | 8 | -0.35 | -0.75 | 0.775 | 0.927 | 1.000 | 444 | tags=13%, list=2%, signal=13% | |
2779 | VENTRICULAR CARDIAC MUSCLE TISSUE MORPHOGENESIS | 38 | -0.23 | -0.75 | 0.807 | 0.928 | 1.000 | 1784 | tags=13%, list=9%, signal=14% | |
2780 | RIBONUCLEOSIDE DIPHOSPHATE METABOLIC PROCESS | 40 | -0.23 | -0.75 | 0.800 | 0.928 | 1.000 | 2064 | tags=13%, list=10%, signal=14% | |
2781 | CELLULAR COMPONENT MAINTENANCE | 9 | -0.33 | -0.75 | 0.760 | 0.928 | 1.000 | 247 | tags=11%, list=1%, signal=11% | |
2782 | CELLULAR RESPONSE TO HISTAMINE | 6 | -0.34 | -0.75 | 0.770 | 0.928 | 1.000 | 13626 | tags=100%, list=66%, signal=295% | |
2783 | POSITIVE REGULATION OF LEUKOCYTE MEDIATED CYTOTOXICITY | 23 | -0.24 | -0.75 | 0.751 | 0.928 | 1.000 | 3208 | tags=17%, list=16%, signal=21% | |
2784 | PYRIMIDINE NUCLEOSIDE CATABOLIC PROCESS | 19 | -0.26 | -0.75 | 0.808 | 0.928 | 1.000 | 6804 | tags=42%, list=33%, signal=63% | |
2785 | GLUCOSE METABOLIC PROCESS | 89 | -0.18 | -0.75 | 0.863 | 0.929 | 1.000 | 4394 | tags=17%, list=21%, signal=21% | |
2786 | SUCCINATE METABOLIC PROCESS | 6 | -0.35 | -0.75 | 0.791 | 0.928 | 1.000 | 5562 | tags=50%, list=27%, signal=68% | |
2787 | REGULATION OF CYTOLYSIS | 8 | -0.33 | -0.75 | 0.763 | 0.928 | 1.000 | 7283 | tags=50%, list=35%, signal=77% | |
2788 | OLFACTORY PLACODE FORMATION | 5 | -0.38 | -0.75 | 0.778 | 0.928 | 1.000 | 6442 | tags=60%, list=31%, signal=87% | |
2789 | OLFACTORY PLACODE DEVELOPMENT | 5 | -0.38 | -0.75 | 0.778 | 0.928 | 1.000 | 6442 | tags=60%, list=31%, signal=87% | |
2790 | OLFACTORY PLACODE MORPHOGENESIS | 5 | -0.38 | -0.75 | 0.778 | 0.927 | 1.000 | 6442 | tags=60%, list=31%, signal=87% | |
2791 | NEGATIVE REGULATION OF TRANSPORT | 250 | -0.16 | -0.75 | 0.962 | 0.928 | 1.000 | 4951 | tags=25%, list=24%, signal=32% | |
2792 | NEGATIVE REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 13 | -0.28 | -0.75 | 0.798 | 0.928 | 1.000 | 5050 | tags=31%, list=25%, signal=41% | |
2793 | POSITIVE REGULATION OF LEUKOCYTE CHEMOTAXIS | 50 | -0.22 | -0.75 | 0.871 | 0.928 | 1.000 | 3192 | tags=18%, list=15%, signal=21% | |
2794 | NEGATIVE REGULATION OF MAPK CASCADE | 92 | -0.19 | -0.75 | 0.908 | 0.928 | 1.000 | 5228 | tags=27%, list=25%, signal=36% | |
2795 | STEROID CATABOLIC PROCESS | 12 | -0.27 | -0.75 | 0.785 | 0.928 | 1.000 | 896 | tags=17%, list=4%, signal=17% | |
2796 | NEGATIVE REGULATION OF COLLATERAL SPROUTING | 9 | -0.31 | -0.75 | 0.812 | 0.927 | 1.000 | 14240 | tags=100%, list=69%, signal=324% | |
2797 | POSITIVE REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 7 | -0.33 | -0.75 | 0.767 | 0.928 | 1.000 | 13772 | tags=100%, list=67%, signal=301% | |
2798 | DECIDUALIZATION | 15 | -0.30 | -0.75 | 0.790 | 0.928 | 1.000 | 4874 | tags=47%, list=24%, signal=61% | |
2799 | LYSINE METABOLIC PROCESS | 9 | -0.31 | -0.75 | 0.769 | 0.928 | 1.000 | 2698 | tags=22%, list=13%, signal=26% | |
2800 | LYSINE CATABOLIC PROCESS | 9 | -0.31 | -0.75 | 0.769 | 0.927 | 1.000 | 2698 | tags=22%, list=13%, signal=26% | |
2801 | MAMMARY GLAND BRANCHING INVOLVED IN PREGNANCY | 5 | -0.38 | -0.75 | 0.769 | 0.927 | 1.000 | 5050 | tags=60%, list=25%, signal=79% | |
2802 | VENOUS BLOOD VESSEL DEVELOPMENT | 17 | -0.25 | -0.75 | 0.819 | 0.927 | 1.000 | 7204 | tags=53%, list=35%, signal=81% | |
2803 | ADULT BEHAVIOR | 37 | -0.22 | -0.75 | 0.802 | 0.927 | 1.000 | 9578 | tags=62%, list=46%, signal=116% | |
2804 | REGULATION OF NATURAL KILLER CELL MEDIATED CYTOTOXICITY | 24 | -0.23 | -0.75 | 0.805 | 0.928 | 1.000 | 3208 | tags=17%, list=16%, signal=20% | |
2805 | NEUROMUSCULAR JUNCTION DEVELOPMENT | 10 | -0.28 | -0.75 | 0.842 | 0.928 | 1.000 | 3170 | tags=30%, list=15%, signal=35% | |
2806 | POSITIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 168 | -0.17 | -0.75 | 0.896 | 0.930 | 1.000 | 6248 | tags=30%, list=30%, signal=43% | |
2807 | CELLULAR RESPONSE TO NUTRIENT | 13 | -0.29 | -0.75 | 0.803 | 0.929 | 1.000 | 2779 | tags=23%, list=13%, signal=27% | |
2808 | SECRETION BY TISSUE | 31 | -0.22 | -0.75 | 0.862 | 0.930 | 1.000 | 3815 | tags=26%, list=19%, signal=32% | |
2809 | NEGATIVE REGULATION OF PROTEIN COMPLEX DISASSEMBLY | 27 | -0.23 | -0.75 | 0.868 | 0.929 | 1.000 | 2471 | tags=15%, list=12%, signal=17% | |
2810 | REGULATION OF INSULIN-LIKE GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 11 | -0.31 | -0.75 | 0.763 | 0.929 | 1.000 | 3800 | tags=27%, list=18%, signal=33% | |
2811 | REGULATION OF TRANSPORTER ACTIVITY | 137 | -0.18 | -0.75 | 0.868 | 0.930 | 1.000 | 6561 | tags=33%, list=32%, signal=48% | |
2812 | FEMALE MEIOTIC DIVISION | 5 | -0.36 | -0.74 | 0.802 | 0.931 | 1.000 | 3961 | tags=60%, list=19%, signal=74% | |
2813 | POSITIVE REGULATION OF LEUKOCYTE MEDIATED IMMUNITY | 45 | -0.22 | -0.74 | 0.844 | 0.931 | 1.000 | 5558 | tags=29%, list=27%, signal=39% | |
2814 | POSITIVE REGULATION OF MYOTUBE DIFFERENTIATION | 12 | -0.31 | -0.74 | 0.729 | 0.931 | 1.000 | 1716 | tags=17%, list=8%, signal=18% | |
2815 | POSITIVE REGULATION OF FILOPODIUM ASSEMBLY | 12 | -0.27 | -0.74 | 0.817 | 0.931 | 1.000 | 1830 | tags=17%, list=9%, signal=18% | |
2816 | RECEPTOR METABOLIC PROCESS | 57 | -0.21 | -0.74 | 0.845 | 0.931 | 1.000 | 4352 | tags=25%, list=21%, signal=31% | |
2817 | RIBOSE PHOSPHATE METABOLIC PROCESS | 169 | -0.17 | -0.74 | 0.927 | 0.931 | 1.000 | 2134 | tags=11%, list=10%, signal=12% | |
2818 | OLFACTORY BULB INTERNEURON DIFFERENTIATION | 11 | -0.30 | -0.74 | 0.788 | 0.931 | 1.000 | 2062 | tags=18%, list=10%, signal=20% | |
2819 | MEMBRANE PROTEIN ECTODOMAIN PROTEOLYSIS | 15 | -0.27 | -0.74 | 0.818 | 0.931 | 1.000 | 1367 | tags=20%, list=7%, signal=21% | |
2820 | SUBPALLIUM DEVELOPMENT | 20 | -0.24 | -0.74 | 0.819 | 0.931 | 1.000 | 4733 | tags=30%, list=23%, signal=39% | |
2821 | VENTRICULAR CARDIAC MUSCLE CELL DEVELOPMENT | 9 | -0.29 | -0.74 | 0.774 | 0.932 | 1.000 | 4823 | tags=33%, list=23%, signal=44% | |
2822 | REGULATION OF INTERLEUKIN-12 PRODUCTION | 35 | -0.22 | -0.74 | 0.837 | 0.932 | 1.000 | 5990 | tags=34%, list=29%, signal=48% | |
2823 | REGULATION OF CALCIUM-MEDIATED SIGNALING | 21 | -0.24 | -0.74 | 0.817 | 0.933 | 1.000 | 2543 | tags=14%, list=12%, signal=16% | |
2824 | REGULATION OF GLYCOLYTIC PROCESS | 19 | -0.26 | -0.74 | 0.810 | 0.932 | 1.000 | 2258 | tags=21%, list=11%, signal=24% | |
2825 | MITRAL VALVE DEVELOPMENT | 8 | -0.33 | -0.74 | 0.809 | 0.932 | 1.000 | 1462 | tags=25%, list=7%, signal=27% | |
2826 | REGULATION OF MYOBLAST FUSION | 8 | -0.37 | -0.74 | 0.735 | 0.933 | 1.000 | 7577 | tags=50%, list=37%, signal=79% | |
2827 | NEGATIVE REGULATION OF CAMP METABOLIC PROCESS | 22 | -0.24 | -0.74 | 0.797 | 0.933 | 1.000 | 5264 | tags=36%, list=26%, signal=49% | |
2828 | INTERMEDIATE FILAMENT BUNDLE ASSEMBLY | 5 | -0.38 | -0.74 | 0.790 | 0.933 | 1.000 | 3694 | tags=40%, list=18%, signal=49% | |
2829 | PURINE-CONTAINING COMPOUND METABOLIC PROCESS | 211 | -0.17 | -0.74 | 0.938 | 0.933 | 1.000 | 4407 | tags=20%, list=21%, signal=25% | |
2830 | EXTRACELLULAR REGULATION OF SIGNAL TRANSDUCTION | 14 | -0.26 | -0.74 | 0.821 | 0.933 | 1.000 | 5856 | tags=36%, list=28%, signal=50% | |
2831 | EXTRACELLULAR NEGATIVE REGULATION OF SIGNAL TRANSDUCTION | 14 | -0.26 | -0.74 | 0.821 | 0.933 | 1.000 | 5856 | tags=36%, list=28%, signal=50% | |
2832 | CHOLESTEROL CATABOLIC PROCESS | 5 | -0.36 | -0.74 | 0.778 | 0.932 | 1.000 | 554 | tags=20%, list=3%, signal=21% | |
2833 | STEROL CATABOLIC PROCESS | 5 | -0.36 | -0.74 | 0.778 | 0.932 | 1.000 | 554 | tags=20%, list=3%, signal=21% | |
2834 | POSITIVE REGULATION OF CD4-POSITIVE, ALPHA-BETA T CELL ACTIVATION | 18 | -0.25 | -0.74 | 0.873 | 0.932 | 1.000 | 5601 | tags=33%, list=27%, signal=46% | |
2835 | REGULATION OF CANONICAL WNT SIGNALING PATHWAY | 178 | -0.17 | -0.74 | 0.887 | 0.932 | 1.000 | 2252 | tags=12%, list=11%, signal=14% | |
2836 | REGULATION OF RELEASE OF SEQUESTERED CALCIUM ION INTO CYTOSOL | 46 | -0.20 | -0.74 | 0.875 | 0.932 | 1.000 | 5630 | tags=30%, list=27%, signal=42% | |
2837 | NEGATIVE REGULATION OF ENDOCYTOSIS | 28 | -0.22 | -0.74 | 0.827 | 0.932 | 1.000 | 3581 | tags=21%, list=17%, signal=26% | |
2838 | BIOMINERAL TISSUE DEVELOPMENT | 43 | -0.21 | -0.74 | 0.848 | 0.932 | 1.000 | 1746 | tags=14%, list=8%, signal=15% | |
2839 | ADULT LOCOMOTORY BEHAVIOR | 11 | -0.26 | -0.74 | 0.782 | 0.932 | 1.000 | 8645 | tags=64%, list=42%, signal=110% | |
2840 | EMBRYONIC PLACENTA DEVELOPMENT | 90 | -0.19 | -0.74 | 0.896 | 0.932 | 1.000 | 2252 | tags=14%, list=11%, signal=16% | |
2841 | OXIDOREDUCTION COENZYME METABOLIC PROCESS | 62 | -0.21 | -0.74 | 0.817 | 0.932 | 1.000 | 4449 | tags=23%, list=22%, signal=29% | |
2842 | ATRIAL SEPTUM DEVELOPMENT | 19 | -0.23 | -0.74 | 0.827 | 0.932 | 1.000 | 4600 | tags=26%, list=22%, signal=34% | |
2843 | ENTRAINMENT OF CIRCADIAN CLOCK BY PHOTOPERIOD | 16 | -0.25 | -0.74 | 0.838 | 0.932 | 1.000 | 5191 | tags=38%, list=25%, signal=50% | |
2844 | GLUTAMINE FAMILY AMINO ACID METABOLIC PROCESS | 32 | -0.23 | -0.74 | 0.805 | 0.933 | 1.000 | 5562 | tags=34%, list=27%, signal=47% | |
2845 | REGULATION OF PROTEIN ACTIVATION CASCADE | 28 | -0.24 | -0.74 | 0.855 | 0.933 | 1.000 | 5376 | tags=39%, list=26%, signal=53% | |
2846 | POSITIVE REGULATION OF TRANSFERASE ACTIVITY | 497 | -0.16 | -0.74 | 0.971 | 0.933 | 1.000 | 5317 | tags=25%, list=26%, signal=32% | |
2847 | SA NODE CELL ACTION POTENTIAL | 6 | -0.35 | -0.74 | 0.797 | 0.933 | 1.000 | 5637 | tags=50%, list=27%, signal=69% | |
2848 | SA NODE CELL TO ATRIAL CARDIAC MUSCLE CELL SIGNALLING | 6 | -0.35 | -0.74 | 0.797 | 0.933 | 1.000 | 5637 | tags=50%, list=27%, signal=69% | |
2849 | SA NODE CELL TO ATRIAL CARDIAC MUSCLE CELL COMMUNICATION | 6 | -0.35 | -0.74 | 0.797 | 0.932 | 1.000 | 5637 | tags=50%, list=27%, signal=69% | |
2850 | CELLULAR RESPONSE TO INTERFERON-ALPHA | 6 | -0.34 | -0.74 | 0.808 | 0.932 | 1.000 | 4557 | tags=33%, list=22%, signal=43% | |
2851 | REGULATION OF LAMELLIPODIUM ORGANIZATION | 20 | -0.25 | -0.74 | 0.814 | 0.932 | 1.000 | 6599 | tags=40%, list=32%, signal=59% | |
2852 | TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 112 | -0.18 | -0.73 | 0.912 | 0.932 | 1.000 | 4591 | tags=21%, list=22%, signal=27% | |
2853 | MONOSACCHARIDE METABOLIC PROCESS | 124 | -0.17 | -0.73 | 0.880 | 0.932 | 1.000 | 4458 | tags=18%, list=22%, signal=23% | |
2854 | MEMBRANE DEPOLARIZATION | 27 | -0.25 | -0.73 | 0.828 | 0.932 | 1.000 | 1207 | tags=11%, list=6%, signal=12% | |
2855 | REGULATION OF CHEMOKINE BIOSYNTHETIC PROCESS | 6 | -0.35 | -0.73 | 0.805 | 0.931 | 1.000 | 741 | tags=17%, list=4%, signal=17% | |
2856 | PROTEIN LOCALIZATION TO CYTOPLASMIC STRESS GRANULE | 7 | -0.36 | -0.73 | 0.764 | 0.932 | 1.000 | 10628 | tags=86%, list=52%, signal=177% | |
2857 | REGULATION OF DENDRITIC CELL CHEMOTAXIS | 7 | -0.34 | -0.73 | 0.786 | 0.932 | 1.000 | 794 | tags=14%, list=4%, signal=15% | |
2858 | POSITIVE REGULATION OF DENDRITIC CELL CHEMOTAXIS | 7 | -0.34 | -0.73 | 0.786 | 0.931 | 1.000 | 794 | tags=14%, list=4%, signal=15% | |
2859 | NEGATIVE REGULATION OF PEPTIDE SECRETION | 16 | -0.25 | -0.73 | 0.817 | 0.933 | 1.000 | 3032 | tags=19%, list=15%, signal=22% | |
2860 | RESPONSE TO ALCOHOL | 74 | -0.18 | -0.73 | 0.936 | 0.933 | 1.000 | 4902 | tags=22%, list=24%, signal=28% | |
2861 | COFACTOR BIOSYNTHETIC PROCESS | 87 | -0.20 | -0.73 | 0.834 | 0.933 | 1.000 | 2867 | tags=18%, list=14%, signal=21% | |
2862 | NEGATIVE REGULATION OF INSULIN SECRETION | 14 | -0.27 | -0.73 | 0.807 | 0.934 | 1.000 | 3032 | tags=21%, list=15%, signal=25% | |
2863 | ORGANIC HYDROXY COMPOUND BIOSYNTHETIC PROCESS | 105 | -0.18 | -0.73 | 0.927 | 0.935 | 1.000 | 2374 | tags=12%, list=12%, signal=14% | |
2864 | NEGATIVE REGULATION OF CELLULAR PROTEIN CATABOLIC PROCESS | 55 | -0.22 | -0.73 | 0.827 | 0.935 | 1.000 | 3533 | tags=20%, list=17%, signal=24% | |
2865 | NEGATIVE REGULATION OF INFLAMMATORY RESPONSE | 35 | -0.21 | -0.73 | 0.851 | 0.936 | 1.000 | 1637 | tags=11%, list=8%, signal=12% | |
2866 | NEGATIVE REGULATION OF CALCIUM ION TRANSPORT | 30 | -0.22 | -0.73 | 0.838 | 0.936 | 1.000 | 3494 | tags=17%, list=17%, signal=20% | |
2867 | REGULATION OF BONE RESORPTION | 12 | -0.29 | -0.73 | 0.780 | 0.937 | 1.000 | 3092 | tags=17%, list=15%, signal=20% | |
2868 | CAMERA-TYPE EYE MORPHOGENESIS | 112 | -0.17 | -0.73 | 0.915 | 0.937 | 1.000 | 7002 | tags=38%, list=34%, signal=56% | |
2869 | NEGATIVE REGULATION OF B CELL APOPTOTIC PROCESS | 6 | -0.31 | -0.73 | 0.837 | 0.936 | 1.000 | 4667 | tags=50%, list=23%, signal=65% | |
2870 | REGULATION OF RUFFLE ASSEMBLY | 11 | -0.30 | -0.73 | 0.832 | 0.936 | 1.000 | 3560 | tags=36%, list=17%, signal=44% | |
2871 | REGULATION OF CARDIAC MUSCLE CELL APOPTOTIC PROCESS | 6 | -0.33 | -0.73 | 0.835 | 0.936 | 1.000 | 13772 | tags=100%, list=67%, signal=301% | |
2872 | CEREBELLAR CORTEX FORMATION | 24 | -0.22 | -0.73 | 0.837 | 0.937 | 1.000 | 8303 | tags=38%, list=40%, signal=63% | |
2873 | CARDIAC VASCULAR SMOOTH MUSCLE CELL DIFFERENTIATION | 5 | -0.37 | -0.73 | 0.813 | 0.937 | 1.000 | 2805 | tags=20%, list=14%, signal=23% | |
2874 | EXCITATORY SYNAPSE ASSEMBLY | 7 | -0.31 | -0.73 | 0.807 | 0.938 | 1.000 | 6710 | tags=57%, list=33%, signal=85% | |
2875 | SKIN MORPHOGENESIS | 8 | -0.30 | -0.72 | 0.812 | 0.939 | 1.000 | 6592 | tags=50%, list=32%, signal=73% | |
2876 | DNA DEMETHYLATION | 12 | -0.26 | -0.72 | 0.835 | 0.940 | 1.000 | 333 | tags=8%, list=2%, signal=8% | |
2877 | HEXOSE METABOLIC PROCESS | 100 | -0.18 | -0.72 | 0.891 | 0.942 | 1.000 | 4458 | tags=18%, list=22%, signal=23% | |
2878 | PEPTIDYL-ARGININE MODIFICATION | 11 | -0.28 | -0.72 | 0.869 | 0.942 | 1.000 | 3006 | tags=18%, list=15%, signal=21% | |
2879 | POSITIVE REGULATION OF CYTOPLASMIC TRANSPORT | 185 | -0.16 | -0.72 | 0.950 | 0.941 | 1.000 | 6248 | tags=30%, list=30%, signal=42% | |
2880 | REGULATION OF ENDOTHELIAL CELL DIFFERENTIATION | 14 | -0.26 | -0.72 | 0.831 | 0.943 | 1.000 | 8841 | tags=64%, list=43%, signal=113% | |
2881 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT5 PROTEIN | 13 | -0.27 | -0.72 | 0.793 | 0.943 | 1.000 | 8617 | tags=54%, list=42%, signal=92% | |
2882 | REGULATION OF OLIGODENDROCYTE PROGENITOR PROLIFERATION | 5 | -0.34 | -0.72 | 0.822 | 0.943 | 1.000 | 5383 | tags=40%, list=26%, signal=54% | |
2883 | NEGATIVE REGULATION OF PEPTIDE HORMONE SECRETION | 15 | -0.26 | -0.72 | 0.826 | 0.944 | 1.000 | 3032 | tags=20%, list=15%, signal=23% | |
2884 | POSITIVE REGULATION OF PROTEIN IMPORT INTO NUCLEUS | 59 | -0.20 | -0.72 | 0.882 | 0.944 | 1.000 | 6248 | tags=34%, list=30%, signal=49% | |
2885 | PEPTIDYL-THREONINE DEPHOSPHORYLATION | 7 | -0.34 | -0.72 | 0.808 | 0.944 | 1.000 | 2834 | tags=43%, list=14%, signal=50% | |
2886 | PEPTIDYL-LYSINE METHYLATION | 34 | -0.23 | -0.72 | 0.845 | 0.944 | 1.000 | 4219 | tags=24%, list=20%, signal=30% | |
2887 | HISTONE LYSINE METHYLATION | 34 | -0.23 | -0.72 | 0.845 | 0.943 | 1.000 | 4219 | tags=24%, list=20%, signal=30% | |
2888 | POSITIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 70 | -0.19 | -0.72 | 0.892 | 0.943 | 1.000 | 6248 | tags=31%, list=30%, signal=45% | |
2889 | PORPHYRIN-CONTAINING COMPOUND METABOLIC PROCESS | 21 | -0.26 | -0.72 | 0.798 | 0.944 | 1.000 | 2414 | tags=19%, list=12%, signal=22% | |
2890 | REGULATION OF NUCLEAR-TRANSCRIBED MRNA CATABOLIC PROCESS, DEADENYLATION-DEPENDENT DECAY | 13 | -0.26 | -0.72 | 0.875 | 0.944 | 1.000 | 47 | tags=8%, list=0%, signal=8% | |
2891 | POSITIVE REGULATION OF NUCLEAR-TRANSCRIBED MRNA CATABOLIC PROCESS, DEADENYLATION-DEPENDENT DECAY | 13 | -0.26 | -0.72 | 0.875 | 0.943 | 1.000 | 47 | tags=8%, list=0%, signal=8% | |
2892 | NEGATIVE REGULATION OF NUCLEOTIDE METABOLIC PROCESS | 32 | -0.23 | -0.72 | 0.829 | 0.943 | 1.000 | 3494 | tags=25%, list=17%, signal=30% | |
2893 | POSITIVE REGULATION OF FAT CELL DIFFERENTIATION | 25 | -0.23 | -0.72 | 0.854 | 0.943 | 1.000 | 980 | tags=12%, list=5%, signal=13% | |
2894 | PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR SIGNALING PATHWAY | 5 | -0.36 | -0.71 | 0.774 | 0.946 | 1.000 | 2933 | tags=40%, list=14%, signal=47% | |
2895 | POSITIVE REGULATION OF MYOBLAST FUSION | 6 | -0.36 | -0.71 | 0.793 | 0.946 | 1.000 | 1001 | tags=17%, list=5%, signal=18% | |
2896 | PRESYNAPTIC MEMBRANE ASSEMBLY | 9 | -0.30 | -0.71 | 0.782 | 0.946 | 1.000 | 6262 | tags=44%, list=30%, signal=64% | |
2897 | NEGATIVE REGULATION OF INNATE IMMUNE RESPONSE | 23 | -0.25 | -0.71 | 0.827 | 0.946 | 1.000 | 3170 | tags=22%, list=15%, signal=26% | |
2898 | PROTEIN REFOLDING | 17 | -0.25 | -0.71 | 0.852 | 0.946 | 1.000 | 4304 | tags=29%, list=21%, signal=37% | |
2899 | POSITIVE REGULATION OF PROTEIN EXPORT FROM NUCLEUS | 9 | -0.27 | -0.71 | 0.852 | 0.946 | 1.000 | 4626 | tags=22%, list=22%, signal=29% | |
2900 | CELLULAR RESPONSE TO CADMIUM ION | 7 | -0.43 | -0.71 | 0.766 | 0.946 | 1.000 | 108 | tags=14%, list=1%, signal=14% | |
2901 | REGULATION OF JAK-STAT CASCADE | 63 | -0.18 | -0.71 | 0.934 | 0.946 | 1.000 | 5089 | tags=25%, list=25%, signal=34% | |
2902 | REGULATION OF STAT CASCADE | 63 | -0.18 | -0.71 | 0.934 | 0.946 | 1.000 | 5089 | tags=25%, list=25%, signal=34% | |
2903 | STEROL METABOLIC PROCESS | 63 | -0.19 | -0.71 | 0.933 | 0.946 | 1.000 | 4498 | tags=22%, list=22%, signal=28% | |
2904 | REGULATION OF SYNAPSE STRUCTURE OR ACTIVITY | 76 | -0.19 | -0.71 | 0.875 | 0.945 | 1.000 | 7022 | tags=42%, list=34%, signal=64% | |
2905 | RECEPTOR INTERNALIZATION | 36 | -0.23 | -0.71 | 0.853 | 0.945 | 1.000 | 3563 | tags=19%, list=17%, signal=23% | |
2906 | COMPLEMENT ACTIVATION | 28 | -0.25 | -0.71 | 0.833 | 0.945 | 1.000 | 7863 | tags=54%, list=38%, signal=87% | |
2907 | NEGATIVE REGULATION OF GLYCOPROTEIN BIOSYNTHETIC PROCESS | 7 | -0.30 | -0.71 | 0.800 | 0.946 | 1.000 | 3512 | tags=29%, list=17%, signal=34% | |
2908 | REGULATION OF PROTEIN IMPORT | 106 | -0.18 | -0.71 | 0.925 | 0.946 | 1.000 | 1789 | tags=11%, list=9%, signal=12% | |
2909 | POSITIVE REGULATION OF WOUND HEALING | 29 | -0.24 | -0.71 | 0.865 | 0.946 | 1.000 | 7097 | tags=48%, list=34%, signal=74% | |
2910 | NEGATIVE REGULATION OF CELL ACTIVATION | 71 | -0.19 | -0.71 | 0.911 | 0.946 | 1.000 | 3650 | tags=20%, list=18%, signal=24% | |
2911 | CARDIAC PACEMAKER CELL DEVELOPMENT | 5 | -0.31 | -0.71 | 0.831 | 0.946 | 1.000 | 7484 | tags=60%, list=36%, signal=94% | |
2912 | POSITIVE REGULATION OF PODOSOME ASSEMBLY | 5 | -0.35 | -0.71 | 0.794 | 0.946 | 1.000 | 8342 | tags=80%, list=40%, signal=134% | |
2913 | NUCLEOSIDE TRIPHOSPHATE CATABOLIC PROCESS | 6 | -0.35 | -0.71 | 0.821 | 0.947 | 1.000 | 2938 | tags=33%, list=14%, signal=39% | |
2914 | NEGATIVE REGULATION OF PROTEIN AUTOPHOSPHORYLATION | 7 | -0.31 | -0.71 | 0.824 | 0.947 | 1.000 | 7138 | tags=57%, list=35%, signal=87% | |
2915 | NEGATIVE REGULATION OF GLUCOCORTICOID RECEPTOR SIGNALING PATHWAY | 6 | -0.31 | -0.71 | 0.846 | 0.947 | 1.000 | 4237 | tags=33%, list=21%, signal=42% | |
2916 | RESPONSE TO ANTIBIOTIC | 16 | -0.24 | -0.71 | 0.915 | 0.947 | 1.000 | 19 | tags=6%, list=0%, signal=6% | |
2917 | REGULATION OF ACTIVATION OF JANUS KINASE ACTIVITY | 7 | -0.32 | -0.71 | 0.827 | 0.947 | 1.000 | 3574 | tags=29%, list=17%, signal=35% | |
2918 | REGULATION OF SKELETAL MUSCLE CELL DIFFERENTIATION | 9 | -0.29 | -0.71 | 0.847 | 0.947 | 1.000 | 6442 | tags=56%, list=31%, signal=81% | |
2919 | REGULATION OF PROTEIN PROCESSING | 50 | -0.20 | -0.71 | 0.916 | 0.948 | 1.000 | 5376 | tags=34%, list=26%, signal=46% | |
2920 | COFACTOR METABOLIC PROCESS | 196 | -0.17 | -0.71 | 0.938 | 0.948 | 1.000 | 3898 | tags=20%, list=19%, signal=24% | |
2921 | POSITIVE REGULATION OF NEUROBLAST PROLIFERATION | 17 | -0.25 | -0.71 | 0.866 | 0.948 | 1.000 | 3650 | tags=29%, list=18%, signal=36% | |
2922 | AMYLOID PRECURSOR PROTEIN METABOLIC PROCESS | 8 | -0.32 | -0.71 | 0.838 | 0.948 | 1.000 | 227 | tags=13%, list=1%, signal=13% | |
2923 | NEGATIVE REGULATION OF LYMPHOCYTE ACTIVATION | 54 | -0.20 | -0.70 | 0.904 | 0.949 | 1.000 | 3650 | tags=20%, list=18%, signal=25% | |
2924 | APOPTOTIC PROCESS INVOLVED IN DEVELOPMENT | 20 | -0.25 | -0.70 | 0.821 | 0.949 | 1.000 | 4206 | tags=25%, list=20%, signal=31% | |
2925 | CIRCADIAN REGULATION OF GENE EXPRESSION | 43 | -0.19 | -0.70 | 0.913 | 0.949 | 1.000 | 4506 | tags=28%, list=22%, signal=36% | |
2926 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO OXIDATIVE STRESS | 7 | -0.30 | -0.70 | 0.858 | 0.949 | 1.000 | 4384 | tags=43%, list=21%, signal=54% | |
2927 | CENTRAL NERVOUS SYSTEM PROJECTION NEURON AXONOGENESIS | 20 | -0.23 | -0.70 | 0.865 | 0.949 | 1.000 | 1085 | tags=10%, list=5%, signal=11% | |
2928 | RESPONSE TO DSRNA | 26 | -0.23 | -0.70 | 0.909 | 0.949 | 1.000 | 3689 | tags=27%, list=18%, signal=33% | |
2929 | NEGATIVE REGULATION OF IMMUNE EFFECTOR PROCESS | 59 | -0.19 | -0.70 | 0.875 | 0.949 | 1.000 | 3840 | tags=22%, list=19%, signal=27% | |
2930 | REGULATION OF ALTERNATIVE MRNA SPLICING, VIA SPLICEOSOME | 14 | -0.28 | -0.70 | 0.814 | 0.949 | 1.000 | 3425 | tags=29%, list=17%, signal=34% | |
2931 | POSITIVE REGULATION OF DEPHOSPHORYLATION | 25 | -0.23 | -0.70 | 0.857 | 0.948 | 1.000 | 6278 | tags=36%, list=30%, signal=52% | |
2932 | POSITIVE REGULATION OF PROTEIN DEPHOSPHORYLATION | 25 | -0.23 | -0.70 | 0.857 | 0.948 | 1.000 | 6278 | tags=36%, list=30%, signal=52% | |
2933 | REGULATION OF MULTICELLULAR ORGANISM GROWTH | 17 | -0.23 | -0.70 | 0.872 | 0.948 | 1.000 | 4902 | tags=24%, list=24%, signal=31% | |
2934 | PERICARDIUM DEVELOPMENT | 16 | -0.24 | -0.70 | 0.855 | 0.948 | 1.000 | 6734 | tags=44%, list=33%, signal=65% | |
2935 | MRNA CLEAVAGE | 9 | -0.34 | -0.70 | 0.764 | 0.949 | 1.000 | 626 | tags=11%, list=3%, signal=11% | |
2936 | PROTEIN DENEDDYLATION | 10 | -0.30 | -0.70 | 0.811 | 0.949 | 1.000 | 5995 | tags=40%, list=29%, signal=56% | |
2937 | POSITIVE REGULATION OF DENDRITE DEVELOPMENT | 34 | -0.20 | -0.70 | 0.906 | 0.949 | 1.000 | 7022 | tags=50%, list=34%, signal=76% | |
2938 | REGULATION OF NUCLEAR CELL CYCLE DNA REPLICATION | 6 | -0.36 | -0.70 | 0.811 | 0.949 | 1.000 | 7099 | tags=67%, list=34%, signal=102% | |
2939 | MUSCLE HYPERTROPHY | 13 | -0.25 | -0.70 | 0.854 | 0.949 | 1.000 | 5630 | tags=46%, list=27%, signal=63% | |
2940 | CYTOKINETIC PROCESS | 8 | -0.29 | -0.70 | 0.879 | 0.949 | 1.000 | 4332 | tags=38%, list=21%, signal=47% | |
2941 | LONG-TERM MEMORY | 7 | -0.30 | -0.70 | 0.869 | 0.949 | 1.000 | 7096 | tags=57%, list=34%, signal=87% | |
2942 | POSITIVE REGULATION OF B CELL PROLIFERATION | 21 | -0.22 | -0.70 | 0.899 | 0.949 | 1.000 | 4961 | tags=29%, list=24%, signal=38% | |
2943 | REGULATION OF PROTEIN MATURATION | 51 | -0.20 | -0.70 | 0.919 | 0.949 | 1.000 | 5376 | tags=33%, list=26%, signal=45% | |
2944 | PEPTIDYL-LYSINE TRIMETHYLATION | 8 | -0.30 | -0.70 | 0.855 | 0.950 | 1.000 | 2258 | tags=25%, list=11%, signal=28% | |
2945 | BILE ACID METABOLIC PROCESS | 35 | -0.21 | -0.70 | 0.908 | 0.950 | 1.000 | 4736 | tags=26%, list=23%, signal=33% | |
2946 | ALCOHOL BIOSYNTHETIC PROCESS | 62 | -0.18 | -0.70 | 0.938 | 0.950 | 1.000 | 6597 | tags=32%, list=32%, signal=47% | |
2947 | BONE REMODELING | 13 | -0.28 | -0.70 | 0.835 | 0.951 | 1.000 | 4047 | tags=23%, list=20%, signal=29% | |
2948 | REGULATION OF PROTEIN TARGETING TO MITOCHONDRION | 79 | -0.18 | -0.70 | 0.924 | 0.950 | 1.000 | 5111 | tags=25%, list=25%, signal=34% | |
2949 | NOSE DEVELOPMENT | 14 | -0.27 | -0.70 | 0.825 | 0.950 | 1.000 | 7300 | tags=50%, list=35%, signal=77% | |
2950 | CELLULAR RESPONSE TO IRON ION | 6 | -0.31 | -0.70 | 0.810 | 0.950 | 1.000 | 5056 | tags=33%, list=25%, signal=44% | |
2951 | LEARNING OR MEMORY | 60 | -0.19 | -0.70 | 0.907 | 0.950 | 1.000 | 7127 | tags=38%, list=35%, signal=58% | |
2952 | REGULATION OF INSULIN SECRETION INVOLVED IN CELLULAR RESPONSE TO GLUCOSE STIMULUS | 15 | -0.25 | -0.70 | 0.821 | 0.950 | 1.000 | 6582 | tags=40%, list=32%, signal=59% | |
2953 | REGULATION OF CALCIUM ION IMPORT | 61 | -0.18 | -0.70 | 0.932 | 0.950 | 1.000 | 7686 | tags=44%, list=37%, signal=70% | |
2954 | STARTLE RESPONSE | 8 | -0.31 | -0.69 | 0.805 | 0.951 | 1.000 | 7686 | tags=63%, list=37%, signal=100% | |
2955 | DETECTION OF MECHANICAL STIMULUS INVOLVED IN SENSORY PERCEPTION | 6 | -0.32 | -0.69 | 0.834 | 0.951 | 1.000 | 7443 | tags=50%, list=36%, signal=78% | |
2956 | POSITIVE REGULATION OF PROTEIN IMPORT | 61 | -0.19 | -0.69 | 0.912 | 0.951 | 1.000 | 6248 | tags=33%, list=30%, signal=47% | |
2957 | ACTIN POLYMERIZATION OR DEPOLYMERIZATION | 20 | -0.24 | -0.69 | 0.862 | 0.952 | 1.000 | 4439 | tags=25%, list=22%, signal=32% | |
2958 | NEGATIVE REGULATION OF ANOIKIS | 16 | -0.25 | -0.69 | 0.878 | 0.952 | 1.000 | 57 | tags=6%, list=0%, signal=6% | |
2959 | RESPONSE TO ALKALOID | 29 | -0.21 | -0.69 | 0.901 | 0.952 | 1.000 | 4628 | tags=24%, list=22%, signal=31% | |
2960 | REGULATION OF CARDIAC MUSCLE CONTRACTION | 47 | -0.19 | -0.69 | 0.911 | 0.952 | 1.000 | 5630 | tags=32%, list=27%, signal=44% | |
2961 | REGULATION OF BONE MINERALIZATION | 37 | -0.20 | -0.69 | 0.930 | 0.953 | 1.000 | 7094 | tags=41%, list=34%, signal=62% | |
2962 | REGULATION OF TRANSMEMBRANE TRANSPORTER ACTIVITY | 128 | -0.17 | -0.69 | 0.911 | 0.953 | 1.000 | 6561 | tags=32%, list=32%, signal=47% | |
2963 | CELLULAR CARBOHYDRATE CATABOLIC PROCESS | 21 | -0.23 | -0.69 | 0.867 | 0.952 | 1.000 | 5094 | tags=24%, list=25%, signal=32% | |
2964 | MRNA MODIFICATION | 7 | -0.32 | -0.69 | 0.837 | 0.952 | 1.000 | 1304 | tags=14%, list=6%, signal=15% | |
2965 | PYRIMIDINE RIBONUCLEOSIDE CATABOLIC PROCESS | 9 | -0.28 | -0.69 | 0.879 | 0.953 | 1.000 | 333 | tags=11%, list=2%, signal=11% | |
2966 | RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 155 | -0.17 | -0.69 | 0.934 | 0.953 | 1.000 | 3050 | tags=16%, list=15%, signal=19% | |
2967 | ACETYL-COA METABOLIC PROCESS | 12 | -0.27 | -0.69 | 0.842 | 0.953 | 1.000 | 2732 | tags=25%, list=13%, signal=29% | |
2968 | REGULATION OF CELL JUNCTION ASSEMBLY | 54 | -0.17 | -0.69 | 0.953 | 0.952 | 1.000 | 3798 | tags=19%, list=18%, signal=23% | |
2969 | CARDIAC MUSCLE CONTRACTION | 42 | -0.20 | -0.69 | 0.904 | 0.952 | 1.000 | 4089 | tags=24%, list=20%, signal=30% | |
2970 | LINOLEIC ACID METABOLIC PROCESS | 13 | -0.25 | -0.69 | 0.871 | 0.952 | 1.000 | 2545 | tags=15%, list=12%, signal=18% | |
2971 | CELLULAR RESPONSE TO ALKALOID | 17 | -0.25 | -0.69 | 0.859 | 0.952 | 1.000 | 9103 | tags=53%, list=44%, signal=95% | |
2972 | NEGATIVE REGULATION OF HISTONE MODIFICATION | 23 | -0.23 | -0.69 | 0.852 | 0.952 | 1.000 | 495 | tags=9%, list=2%, signal=9% | |
2973 | CYTIDINE CATABOLIC PROCESS | 8 | -0.30 | -0.69 | 0.827 | 0.953 | 1.000 | 333 | tags=13%, list=2%, signal=13% | |
2974 | CYTIDINE DEAMINATION | 8 | -0.30 | -0.69 | 0.827 | 0.953 | 1.000 | 333 | tags=13%, list=2%, signal=13% | |
2975 | CYTIDINE METABOLIC PROCESS | 8 | -0.30 | -0.69 | 0.827 | 0.952 | 1.000 | 333 | tags=13%, list=2%, signal=13% | |
2976 | REGULATION OF ENTRY OF BACTERIUM INTO HOST CELL | 5 | -0.34 | -0.69 | 0.847 | 0.953 | 1.000 | 3560 | tags=40%, list=17%, signal=48% | |
2977 | MEMBRANE ASSEMBLY | 25 | -0.22 | -0.69 | 0.872 | 0.952 | 1.000 | 7577 | tags=40%, list=37%, signal=63% | |
2978 | NEGATIVE REGULATION OF JUN KINASE ACTIVITY | 8 | -0.29 | -0.69 | 0.862 | 0.952 | 1.000 | 515 | tags=13%, list=2%, signal=13% | |
2979 | TISSUE REGENERATION | 25 | -0.21 | -0.69 | 0.914 | 0.952 | 1.000 | 6115 | tags=32%, list=30%, signal=45% | |
2980 | REGULATION OF PROTEIN LOCALIZATION TO CELL SURFACE | 18 | -0.23 | -0.69 | 0.905 | 0.953 | 1.000 | 4050 | tags=22%, list=20%, signal=28% | |
2981 | REGULATION OF GRANULOCYTE CHEMOTAXIS | 23 | -0.23 | -0.69 | 0.909 | 0.952 | 1.000 | 794 | tags=9%, list=4%, signal=9% | |
2982 | MULTI-ORGANISM BEHAVIOR | 25 | -0.21 | -0.68 | 0.875 | 0.953 | 1.000 | 4719 | tags=28%, list=23%, signal=36% | |
2983 | REGULATION OF CELL ADHESION MEDIATED BY INTEGRIN | 29 | -0.23 | -0.68 | 0.902 | 0.953 | 1.000 | 2818 | tags=21%, list=14%, signal=24% | |
2984 | REGULATION OF ICOSANOID SECRETION | 9 | -0.31 | -0.68 | 0.829 | 0.952 | 1.000 | 4843 | tags=33%, list=24%, signal=44% | |
2985 | REGULATION OF SYNAPTIC PLASTICITY | 46 | -0.20 | -0.68 | 0.889 | 0.953 | 1.000 | 6965 | tags=41%, list=34%, signal=62% | |
2986 | REGULATION OF CARDIAC MUSCLE CELL DIFFERENTIATION | 11 | -0.28 | -0.68 | 0.865 | 0.952 | 1.000 | 5287 | tags=36%, list=26%, signal=49% | |
2987 | REGULATION OF COMPLEMENT ACTIVATION | 27 | -0.22 | -0.68 | 0.917 | 0.953 | 1.000 | 5376 | tags=37%, list=26%, signal=50% | |
2988 | PURINE RIBONUCLEOTIDE BIOSYNTHETIC PROCESS | 65 | -0.18 | -0.68 | 0.913 | 0.952 | 1.000 | 2829 | tags=14%, list=14%, signal=16% | |
2989 | DNA DUPLEX UNWINDING | 39 | -0.24 | -0.68 | 0.842 | 0.953 | 1.000 | 828 | tags=13%, list=4%, signal=13% | |
2990 | POSITIVE REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 8 | -0.30 | -0.68 | 0.877 | 0.954 | 1.000 | 14470 | tags=100%, list=70%, signal=336% | |
2991 | REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE BY P53 CLASS MEDIATOR | 7 | -0.30 | -0.68 | 0.843 | 0.955 | 1.000 | 4010 | tags=29%, list=19%, signal=35% | |
2992 | NEGATIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE BY P53 CLASS MEDIATOR | 7 | -0.30 | -0.68 | 0.843 | 0.954 | 1.000 | 4010 | tags=29%, list=19%, signal=35% | |
2993 | REGULATION OF CARBOHYDRATE CATABOLIC PROCESS | 21 | -0.23 | -0.68 | 0.870 | 0.954 | 1.000 | 2258 | tags=19%, list=11%, signal=21% | |
2994 | REGULATION OF CELLULAR CARBOHYDRATE CATABOLIC PROCESS | 21 | -0.23 | -0.68 | 0.870 | 0.954 | 1.000 | 2258 | tags=19%, list=11%, signal=21% | |
2995 | NEGATIVE REGULATION OF RECEPTOR BINDING | 11 | -0.25 | -0.68 | 0.850 | 0.954 | 1.000 | 3799 | tags=18%, list=18%, signal=22% | |
2996 | KETONE BIOSYNTHETIC PROCESS | 17 | -0.25 | -0.68 | 0.858 | 0.954 | 1.000 | 2867 | tags=18%, list=14%, signal=20% | |
2997 | REGULATION OF LEUKOCYTE MEDIATED IMMUNITY | 83 | -0.18 | -0.68 | 0.920 | 0.954 | 1.000 | 3840 | tags=20%, list=19%, signal=25% | |
2998 | ANATOMICAL STRUCTURE MATURATION | 46 | -0.19 | -0.68 | 0.929 | 0.955 | 1.000 | 4628 | tags=28%, list=22%, signal=36% | |
2999 | REGULATION OF RECEPTOR CATABOLIC PROCESS | 7 | -0.31 | -0.68 | 0.880 | 0.955 | 1.000 | 4804 | tags=29%, list=23%, signal=37% | |
3000 | POSITIVE REGULATION OF BONE RESORPTION | 5 | -0.35 | -0.68 | 0.840 | 0.955 | 1.000 | 9381 | tags=60%, list=46%, signal=110% | |
3001 | POSITIVE REGULATION OF BONE REMODELING | 5 | -0.35 | -0.68 | 0.840 | 0.954 | 1.000 | 9381 | tags=60%, list=46%, signal=110% | |
3002 | MEMBRANE BIOGENESIS | 27 | -0.21 | -0.68 | 0.901 | 0.955 | 1.000 | 7577 | tags=37%, list=37%, signal=58% | |
3003 | GAS HOMEOSTASIS | 5 | -0.35 | -0.68 | 0.852 | 0.955 | 1.000 | 3560 | tags=40%, list=17%, signal=48% | |
3004 | PHENOL-CONTAINING COMPOUND BIOSYNTHETIC PROCESS | 15 | -0.26 | -0.68 | 0.861 | 0.955 | 1.000 | 160 | tags=7%, list=1%, signal=7% | |
3005 | URETERIC BUD FORMATION | 5 | -0.33 | -0.67 | 0.855 | 0.956 | 1.000 | 6144 | tags=60%, list=30%, signal=85% | |
3006 | REGULATION OF TELOMERASE RNA LOCALIZATION TO CAJAL BODY | 12 | -0.33 | -0.67 | 0.742 | 0.957 | 1.000 | 3382 | tags=17%, list=16%, signal=20% | |
3007 | POSITIVE REGULATION OF TELOMERASE RNA LOCALIZATION TO CAJAL BODY | 12 | -0.33 | -0.67 | 0.742 | 0.956 | 1.000 | 3382 | tags=17%, list=16%, signal=20% | |
3008 | NEGATIVE REGULATION OF LIPID CATABOLIC PROCESS | 12 | -0.25 | -0.67 | 0.909 | 0.956 | 1.000 | 3155 | tags=25%, list=15%, signal=30% | |
3009 | RIBONUCLEOTIDE BIOSYNTHETIC PROCESS | 66 | -0.18 | -0.67 | 0.926 | 0.956 | 1.000 | 2829 | tags=14%, list=14%, signal=16% | |
3010 | SNRNA METABOLIC PROCESS | 19 | -0.24 | -0.67 | 0.861 | 0.956 | 1.000 | 5129 | tags=32%, list=25%, signal=42% | |
3011 | BONE CELL DEVELOPMENT | 19 | -0.23 | -0.67 | 0.884 | 0.957 | 1.000 | 1038 | tags=11%, list=5%, signal=11% | |
3012 | REGULATION OF SPROUTING ANGIOGENESIS | 21 | -0.21 | -0.67 | 0.919 | 0.957 | 1.000 | 6245 | tags=38%, list=30%, signal=55% | |
3013 | HISTONE METHYLATION | 46 | -0.21 | -0.67 | 0.881 | 0.957 | 1.000 | 4443 | tags=24%, list=22%, signal=30% | |
3014 | EMBRYONIC EYE MORPHOGENESIS | 36 | -0.20 | -0.67 | 0.884 | 0.956 | 1.000 | 7300 | tags=44%, list=35%, signal=69% | |
3015 | RIBOSE PHOSPHATE BIOSYNTHETIC PROCESS | 68 | -0.18 | -0.67 | 0.926 | 0.956 | 1.000 | 2829 | tags=13%, list=14%, signal=15% | |
3016 | POSITIVE REGULATION OF SEQUESTERING OF CALCIUM ION | 10 | -0.26 | -0.67 | 0.880 | 0.957 | 1.000 | 6521 | tags=30%, list=32%, signal=44% | |
3017 | REGULATION OF NEUROBLAST PROLIFERATION | 24 | -0.23 | -0.67 | 0.916 | 0.956 | 1.000 | 3650 | tags=25%, list=18%, signal=30% | |
3018 | CELL CHEMOTAXIS | 105 | -0.18 | -0.67 | 0.957 | 0.958 | 1.000 | 5650 | tags=30%, list=27%, signal=40% | |
3019 | POSITIVE REGULATION OF CELL KILLING | 25 | -0.21 | -0.67 | 0.874 | 0.958 | 1.000 | 3208 | tags=16%, list=16%, signal=19% | |
3020 | DRUG TRANSMEMBRANE TRANSPORT | 13 | -0.25 | -0.67 | 0.890 | 0.960 | 1.000 | 6597 | tags=46%, list=32%, signal=68% | |
3021 | BETA-AMYLOID METABOLIC PROCESS | 6 | -0.30 | -0.67 | 0.870 | 0.959 | 1.000 | 1479 | tags=17%, list=7%, signal=18% | |
3022 | MICROTUBULE NUCLEATION | 10 | -0.28 | -0.67 | 0.829 | 0.959 | 1.000 | 370 | tags=10%, list=2%, signal=10% | |
3023 | STEROID BIOSYNTHETIC PROCESS | 76 | -0.17 | -0.67 | 0.939 | 0.959 | 1.000 | 7660 | tags=42%, list=37%, signal=67% | |
3024 | REGULATION OF SYNAPSE ORGANIZATION | 38 | -0.20 | -0.67 | 0.907 | 0.960 | 1.000 | 7022 | tags=42%, list=34%, signal=64% | |
3025 | MICROTUBULE POLYMERIZATION OR DEPOLYMERIZATION | 21 | -0.23 | -0.67 | 0.908 | 0.959 | 1.000 | 5504 | tags=24%, list=27%, signal=32% | |
3026 | KERATINOCYTE PROLIFERATION | 5 | -0.33 | -0.66 | 0.875 | 0.959 | 1.000 | 6611 | tags=40%, list=32%, signal=59% | |
3027 | GALACTOSE CATABOLIC PROCESS | 5 | -0.31 | -0.66 | 0.861 | 0.959 | 1.000 | 4458 | tags=40%, list=22%, signal=51% | |
3028 | REGULATION OF TRANSPOSITION | 8 | -0.30 | -0.66 | 0.902 | 0.959 | 1.000 | 333 | tags=13%, list=2%, signal=13% | |
3029 | NEGATIVE REGULATION OF TRANSPOSITION | 8 | -0.30 | -0.66 | 0.902 | 0.959 | 1.000 | 333 | tags=13%, list=2%, signal=13% | |
3030 | GLUTAMATE RECEPTOR SIGNALING PATHWAY | 33 | -0.20 | -0.66 | 0.906 | 0.960 | 1.000 | 7127 | tags=45%, list=35%, signal=69% | |
3031 | CELLULAR RESPONSE TO UV | 46 | -0.19 | -0.66 | 0.954 | 0.960 | 1.000 | 4746 | tags=24%, list=23%, signal=31% | |
3032 | GLOMERULUS MORPHOGENESIS | 8 | -0.30 | -0.66 | 0.883 | 0.961 | 1.000 | 1523 | tags=25%, list=7%, signal=27% | |
3033 | REGULATION OF ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 126 | -0.16 | -0.66 | 0.939 | 0.961 | 1.000 | 6561 | tags=32%, list=32%, signal=46% | |
3034 | MRNA TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 9 | -0.25 | -0.66 | 0.894 | 0.961 | 1.000 | 475 | tags=11%, list=2%, signal=11% | |
3035 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO STRESS | 19 | -0.23 | -0.66 | 0.928 | 0.961 | 1.000 | 4384 | tags=26%, list=21%, signal=33% | |
3036 | ACTIN FILAMENT BUNDLE ASSEMBLY | 29 | -0.20 | -0.66 | 0.942 | 0.961 | 1.000 | 3335 | tags=17%, list=16%, signal=21% | |
3037 | ACTIN FILAMENT BUNDLE ORGANIZATION | 29 | -0.20 | -0.66 | 0.942 | 0.961 | 1.000 | 3335 | tags=17%, list=16%, signal=21% | |
3038 | RECEPTOR RECYCLING | 5 | -0.32 | -0.66 | 0.857 | 0.961 | 1.000 | 6043 | tags=60%, list=29%, signal=85% | |
3039 | CILIUM ORGANIZATION | 125 | -0.16 | -0.66 | 0.977 | 0.961 | 1.000 | 6771 | tags=37%, list=33%, signal=54% | |
3040 | CAVEOLIN-MEDIATED ENDOCYTOSIS | 5 | -0.34 | -0.66 | 0.889 | 0.962 | 1.000 | 3560 | tags=40%, list=17%, signal=48% | |
3041 | REGULATION OF CHEMOKINE (C-X-C MOTIF) LIGAND 2 PRODUCTION | 5 | -0.33 | -0.66 | 0.861 | 0.962 | 1.000 | 1637 | tags=20%, list=8%, signal=22% | |
3042 | REGULATION OF LONG-TERM NEURONAL SYNAPTIC PLASTICITY | 9 | -0.29 | -0.66 | 0.885 | 0.963 | 1.000 | 6837 | tags=56%, list=33%, signal=83% | |
3043 | REGULATION OF DEPHOSPHORYLATION | 90 | -0.17 | -0.66 | 0.971 | 0.963 | 1.000 | 6762 | tags=33%, list=33%, signal=49% | |
3044 | REGULATION OF PROTEIN TARGETING | 192 | -0.15 | -0.65 | 0.994 | 0.963 | 1.000 | 5767 | tags=26%, list=28%, signal=35% | |
3045 | NEUROTRANSMITTER BIOSYNTHETIC PROCESS | 10 | -0.27 | -0.65 | 0.848 | 0.965 | 1.000 | 7542 | tags=50%, list=37%, signal=79% | |
3046 | REGULATION OF PROTEIN DEPHOSPHORYLATION | 87 | -0.16 | -0.65 | 0.971 | 0.965 | 1.000 | 6762 | tags=33%, list=33%, signal=49% | |
3047 | PROTEIN LOCALIZATION TO CELL SURFACE | 17 | -0.21 | -0.65 | 0.948 | 0.965 | 1.000 | 3815 | tags=24%, list=19%, signal=29% | |
3048 | POSITIVE REGULATION OF TRANSCRIPTION REGULATORY REGION DNA BINDING | 10 | -0.25 | -0.65 | 0.908 | 0.964 | 1.000 | 4557 | tags=30%, list=22%, signal=38% | |
3049 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA PRODUCTION | 16 | -0.26 | -0.65 | 0.932 | 0.964 | 1.000 | 7713 | tags=50%, list=37%, signal=80% | |
3050 | POSITIVE REGULATION OF CELL-SUBSTRATE ADHESION | 46 | -0.18 | -0.65 | 0.967 | 0.965 | 1.000 | 7468 | tags=41%, list=36%, signal=65% | |
3051 | CELL PROLIFERATION INVOLVED IN KIDNEY DEVELOPMENT | 10 | -0.28 | -0.65 | 0.897 | 0.965 | 1.000 | 7031 | tags=60%, list=34%, signal=91% | |
3052 | BUNDLE OF HIS CELL TO PURKINJE MYOCYTE COMMUNICATION | 11 | -0.27 | -0.65 | 0.853 | 0.965 | 1.000 | 5327 | tags=45%, list=26%, signal=61% | |
3053 | PLASMA MEMBRANE RAFT ASSEMBLY | 5 | -0.35 | -0.65 | 0.886 | 0.965 | 1.000 | 7577 | tags=60%, list=37%, signal=95% | |
3054 | PLASMA MEMBRANE RAFT ORGANIZATION | 5 | -0.35 | -0.65 | 0.886 | 0.965 | 1.000 | 7577 | tags=60%, list=37%, signal=95% | |
3055 | REGULATION OF T CELL MEDIATED IMMUNITY | 36 | -0.18 | -0.65 | 0.937 | 0.965 | 1.000 | 3350 | tags=17%, list=16%, signal=20% | |
3056 | PHOTOPERIODISM | 17 | -0.22 | -0.65 | 0.903 | 0.965 | 1.000 | 5191 | tags=35%, list=25%, signal=47% | |
3057 | POSITIVE REGULATION OF POTASSIUM ION TRANSPORT | 22 | -0.21 | -0.65 | 0.931 | 0.965 | 1.000 | 2829 | tags=18%, list=14%, signal=21% | |
3058 | REGULATION OF PHOSPHATASE ACTIVITY | 76 | -0.16 | -0.65 | 0.970 | 0.965 | 1.000 | 2480 | tags=13%, list=12%, signal=15% | |
3059 | POSITIVE REGULATION OF DNA REPAIR | 24 | -0.21 | -0.65 | 0.902 | 0.966 | 1.000 | 4380 | tags=29%, list=21%, signal=37% | |
3060 | ORGAN MATURATION | 16 | -0.22 | -0.65 | 0.899 | 0.966 | 1.000 | 4557 | tags=31%, list=22%, signal=40% | |
3061 | POSITIVE REGULATION OF ACTIVIN RECEPTOR SIGNALING PATHWAY | 6 | -0.27 | -0.65 | 0.867 | 0.966 | 1.000 | 7842 | tags=67%, list=38%, signal=108% | |
3062 | VASCULAR SMOOTH MUSCLE CELL DEVELOPMENT | 6 | -0.31 | -0.65 | 0.909 | 0.967 | 1.000 | 1413 | tags=17%, list=7%, signal=18% | |
3063 | POSITIVE REGULATION OF DENDRITIC SPINE DEVELOPMENT | 16 | -0.22 | -0.64 | 0.933 | 0.967 | 1.000 | 7388 | tags=50%, list=36%, signal=78% | |
3064 | POSITIVE REGULATION OF ANION TRANSPORT | 20 | -0.21 | -0.64 | 0.932 | 0.967 | 1.000 | 4843 | tags=30%, list=24%, signal=39% | |
3065 | REGULATION OF GLUCOCORTICOID RECEPTOR SIGNALING PATHWAY | 7 | -0.26 | -0.64 | 0.917 | 0.967 | 1.000 | 4237 | tags=29%, list=21%, signal=36% | |
3066 | CENTRAL NERVOUS SYSTEM MYELINATION | 11 | -0.25 | -0.64 | 0.903 | 0.967 | 1.000 | 396 | tags=9%, list=2%, signal=9% | |
3067 | AXON ENSHEATHMENT IN CENTRAL NERVOUS SYSTEM | 11 | -0.25 | -0.64 | 0.903 | 0.967 | 1.000 | 396 | tags=9%, list=2%, signal=9% | |
3068 | FOREBRAIN DORSAL/VENTRAL PATTERN FORMATION | 5 | -0.35 | -0.64 | 0.898 | 0.967 | 1.000 | 6025 | tags=40%, list=29%, signal=57% | |
3069 | LEUKOTRIENE BIOSYNTHETIC PROCESS | 8 | -0.28 | -0.64 | 0.900 | 0.967 | 1.000 | 2623 | tags=25%, list=13%, signal=29% | |
3070 | LOW-DENSITY LIPOPROTEIN PARTICLE REMODELING | 8 | -0.28 | -0.64 | 0.910 | 0.968 | 1.000 | 7455 | tags=63%, list=36%, signal=98% | |
3071 | ER OVERLOAD RESPONSE | 5 | -0.29 | -0.64 | 0.934 | 0.967 | 1.000 | 1277 | tags=20%, list=6%, signal=21% | |
3072 | NEGATIVE REGULATION OF ENDOPLASMIC RETICULUM UNFOLDED PROTEIN RESPONSE | 8 | -0.28 | -0.64 | 0.889 | 0.968 | 1.000 | 5743 | tags=38%, list=28%, signal=52% | |
3073 | LAYER FORMATION IN CEREBRAL CORTEX | 13 | -0.23 | -0.64 | 0.942 | 0.968 | 1.000 | 257 | tags=8%, list=1%, signal=8% | |
3074 | CELL SURFACE RECEPTOR SIGNALING PATHWAY INVOLVED IN HEART DEVELOPMENT | 14 | -0.23 | -0.64 | 0.899 | 0.968 | 1.000 | 1523 | tags=14%, list=7%, signal=15% | |
3075 | NEGATIVE REGULATION OF JAK-STAT CASCADE | 7 | -0.29 | -0.64 | 0.929 | 0.968 | 1.000 | 8776 | tags=57%, list=43%, signal=100% | |
3076 | NEGATIVE REGULATION OF STAT CASCADE | 7 | -0.29 | -0.64 | 0.929 | 0.968 | 1.000 | 8776 | tags=57%, list=43%, signal=100% | |
3077 | INNER EAR RECEPTOR STEREOCILIUM ORGANIZATION | 32 | -0.17 | -0.64 | 0.953 | 0.968 | 1.000 | 2826 | tags=16%, list=14%, signal=18% | |
3078 | NEGATIVE REGULATION OF DNA REPAIR | 10 | -0.23 | -0.64 | 0.910 | 0.968 | 1.000 | 9800 | tags=60%, list=48%, signal=114% | |
3079 | SEGMENT SPECIFICATION | 11 | -0.23 | -0.64 | 0.932 | 0.968 | 1.000 | 451 | tags=9%, list=2%, signal=9% | |
3080 | RESPONSE TO VITAMIN | 15 | -0.23 | -0.63 | 0.936 | 0.970 | 1.000 | 1345 | tags=13%, list=7%, signal=14% | |
3081 | NEGATIVE REGULATION OF CELLULAR EXTRAVASATION | 6 | -0.29 | -0.63 | 0.916 | 0.969 | 1.000 | 6916 | tags=67%, list=34%, signal=100% | |
3082 | NEGATIVE REGULATION OF RECEPTOR-MEDIATED ENDOCYTOSIS | 14 | -0.21 | -0.63 | 0.927 | 0.970 | 1.000 | 3581 | tags=21%, list=17%, signal=26% | |
3083 | ESTABLISHMENT OR MAINTENANCE OF EPITHELIAL CELL APICAL/BASAL POLARITY | 11 | -0.24 | -0.63 | 0.896 | 0.970 | 1.000 | 6789 | tags=55%, list=33%, signal=81% | |
3084 | ACTION POTENTIAL | 41 | -0.19 | -0.63 | 0.917 | 0.970 | 1.000 | 5637 | tags=29%, list=27%, signal=40% | |
3085 | EMBRYONIC CAMERA-TYPE EYE FORMATION | 13 | -0.21 | -0.63 | 0.918 | 0.971 | 1.000 | 8151 | tags=62%, list=40%, signal=102% | |
3086 | DNA METHYLATION ON CYTOSINE | 8 | -0.26 | -0.63 | 0.890 | 0.972 | 1.000 | 5491 | tags=38%, list=27%, signal=51% | |
3087 | EPITHELIAL CELL PROLIFERATION INVOLVED IN SALIVARY GLAND MORPHOGENESIS | 7 | -0.29 | -0.63 | 0.932 | 0.973 | 1.000 | 5650 | tags=43%, list=27%, signal=59% | |
3088 | PEPTIDYL-TYROSINE AUTOPHOSPHORYLATION | 8 | -0.27 | -0.63 | 0.905 | 0.973 | 1.000 | 5297 | tags=38%, list=26%, signal=50% | |
3089 | MODULATION OF EXCITATORY POSTSYNAPTIC POTENTIAL | 18 | -0.22 | -0.63 | 0.921 | 0.974 | 1.000 | 7611 | tags=50%, list=37%, signal=79% | |
3090 | MACROPHAGE CHEMOTAXIS | 8 | -0.27 | -0.63 | 0.927 | 0.973 | 1.000 | 6719 | tags=50%, list=33%, signal=74% | |
3091 | NEGATIVE REGULATION OF DOUBLE-STRAND BREAK REPAIR | 9 | -0.24 | -0.63 | 0.927 | 0.973 | 1.000 | 6504 | tags=33%, list=32%, signal=49% | |
3092 | PATTERNING OF BLOOD VESSELS | 37 | -0.17 | -0.63 | 0.962 | 0.973 | 1.000 | 6234 | tags=32%, list=30%, signal=46% | |
3093 | POST-EMBRYONIC CAMERA-TYPE EYE DEVELOPMENT | 7 | -0.27 | -0.63 | 0.932 | 0.973 | 1.000 | 1637 | tags=14%, list=8%, signal=16% | |
3094 | REGULATION OF PLATELET AGGREGATION | 10 | -0.26 | -0.62 | 0.926 | 0.974 | 1.000 | 239 | tags=10%, list=1%, signal=10% | |
3095 | MICROTUBULE BUNDLE FORMATION | 42 | -0.17 | -0.62 | 0.979 | 0.974 | 1.000 | 6569 | tags=33%, list=32%, signal=49% | |
3096 | RESPONSE TO EPIDERMAL GROWTH FACTOR | 13 | -0.23 | -0.62 | 0.893 | 0.975 | 1.000 | 1985 | tags=15%, list=10%, signal=17% | |
3097 | REGULATION OF ALDOSTERONE METABOLIC PROCESS | 6 | -0.30 | -0.62 | 0.906 | 0.974 | 1.000 | 5050 | tags=50%, list=25%, signal=66% | |
3098 | REGULATION OF ALDOSTERONE BIOSYNTHETIC PROCESS | 6 | -0.30 | -0.62 | 0.906 | 0.974 | 1.000 | 5050 | tags=50%, list=25%, signal=66% | |
3099 | REGULATION OF STEROID HORMONE BIOSYNTHETIC PROCESS | 6 | -0.30 | -0.62 | 0.906 | 0.974 | 1.000 | 5050 | tags=50%, list=25%, signal=66% | |
3100 | POSITIVE REGULATION OF LIPID CATABOLIC PROCESS | 19 | -0.20 | -0.62 | 0.970 | 0.974 | 1.000 | 4193 | tags=26%, list=20%, signal=33% | |
3101 | CELLULAR MODIFIED AMINO ACID METABOLIC PROCESS | 205 | -0.12 | -0.62 | 0.984 | 0.973 | 1.000 | 7441 | tags=32%, list=36%, signal=49% | |
3102 | CILIUM ASSEMBLY | 118 | -0.16 | -0.62 | 0.992 | 0.973 | 1.000 | 5901 | tags=31%, list=29%, signal=43% | |
3103 | INTRA-S DNA DAMAGE CHECKPOINT | 5 | -0.32 | -0.62 | 0.901 | 0.973 | 1.000 | 5928 | tags=60%, list=29%, signal=84% | |
3104 | POSITIVE REGULATION OF ACTIVATION OF JAK2 KINASE ACTIVITY | 5 | -0.31 | -0.62 | 0.879 | 0.973 | 1.000 | 7793 | tags=40%, list=38%, signal=64% | |
3105 | POSITIVE REGULATION OF MRNA PROCESSING | 18 | -0.25 | -0.62 | 0.907 | 0.973 | 1.000 | 3172 | tags=17%, list=15%, signal=20% | |
3106 | REGULATION OF RNA SPLICING | 45 | -0.19 | -0.62 | 0.911 | 0.973 | 1.000 | 5642 | tags=29%, list=27%, signal=40% | |
3107 | SEMINIFEROUS TUBULE DEVELOPMENT | 13 | -0.22 | -0.62 | 0.928 | 0.973 | 1.000 | 5944 | tags=38%, list=29%, signal=54% | |
3108 | POSITIVE REGULATION OF INTERLEUKIN-13 PRODUCTION | 9 | -0.25 | -0.62 | 0.946 | 0.974 | 1.000 | 4557 | tags=33%, list=22%, signal=43% | |
3109 | POLYSACCHARIDE BIOSYNTHETIC PROCESS | 25 | -0.19 | -0.62 | 0.923 | 0.974 | 1.000 | 4238 | tags=20%, list=21%, signal=25% | |
3110 | CELLULAR POLYSACCHARIDE BIOSYNTHETIC PROCESS | 25 | -0.19 | -0.62 | 0.923 | 0.974 | 1.000 | 4238 | tags=20%, list=21%, signal=25% | |
3111 | POSITIVE REGULATION OF TOLERANCE INDUCTION | 5 | -0.31 | -0.61 | 0.894 | 0.976 | 1.000 | 2471 | tags=20%, list=12%, signal=23% | |
3112 | MECHANOSENSORY BEHAVIOR | 5 | -0.30 | -0.61 | 0.913 | 0.976 | 1.000 | 1860 | tags=20%, list=9%, signal=22% | |
3113 | RESPONSE TO AUDITORY STIMULUS | 5 | -0.30 | -0.61 | 0.913 | 0.976 | 1.000 | 1860 | tags=20%, list=9%, signal=22% | |
3114 | AUDITORY BEHAVIOR | 5 | -0.30 | -0.61 | 0.913 | 0.975 | 1.000 | 1860 | tags=20%, list=9%, signal=22% | |
3115 | VOCAL LEARNING | 5 | -0.30 | -0.61 | 0.913 | 0.975 | 1.000 | 1860 | tags=20%, list=9%, signal=22% | |
3116 | IMITATIVE LEARNING | 5 | -0.30 | -0.61 | 0.913 | 0.975 | 1.000 | 1860 | tags=20%, list=9%, signal=22% | |
3117 | OBSERVATIONAL LEARNING | 5 | -0.30 | -0.61 | 0.913 | 0.974 | 1.000 | 1860 | tags=20%, list=9%, signal=22% | |
3118 | LEARNED VOCALIZATION BEHAVIOR OR VOCAL LEARNING | 5 | -0.30 | -0.61 | 0.913 | 0.974 | 1.000 | 1860 | tags=20%, list=9%, signal=22% | |
3119 | APOPTOTIC PROCESS INVOLVED IN MORPHOGENESIS | 16 | -0.21 | -0.61 | 0.924 | 0.975 | 1.000 | 4206 | tags=25%, list=20%, signal=31% | |
3120 | NEGATIVE REGULATION OF CHROMATIN MODIFICATION | 28 | -0.20 | -0.61 | 0.925 | 0.975 | 1.000 | 495 | tags=7%, list=2%, signal=7% | |
3121 | VENTRICULAR TRABECULA MYOCARDIUM MORPHOGENESIS | 9 | -0.26 | -0.61 | 0.933 | 0.975 | 1.000 | 6734 | tags=44%, list=33%, signal=66% | |
3122 | CELLULAR RESPONSE TO UV-B | 8 | -0.29 | -0.61 | 0.920 | 0.975 | 1.000 | 5836 | tags=38%, list=28%, signal=52% | |
3123 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT3 PROTEIN | 25 | -0.19 | -0.61 | 0.959 | 0.976 | 1.000 | 4961 | tags=24%, list=24%, signal=32% | |
3124 | CARDIAC MUSCLE HYPERTROPHY | 10 | -0.24 | -0.61 | 0.927 | 0.976 | 1.000 | 5630 | tags=40%, list=27%, signal=55% | |
3125 | OSSIFICATION INVOLVED IN BONE MATURATION | 10 | -0.24 | -0.61 | 0.918 | 0.976 | 1.000 | 3818 | tags=30%, list=19%, signal=37% | |
3126 | HAIR CYCLE PHASE | 13 | -0.23 | -0.61 | 0.955 | 0.977 | 1.000 | 4628 | tags=38%, list=22%, signal=50% | |
3127 | HOMOLOGOUS CHROMOSOME SEGREGATION | 7 | -0.27 | -0.61 | 0.938 | 0.977 | 1.000 | 4474 | tags=29%, list=22%, signal=36% | |
3128 | HIGH-DENSITY LIPOPROTEIN PARTICLE CLEARANCE | 5 | -0.32 | -0.60 | 0.913 | 0.977 | 1.000 | 5414 | tags=40%, list=26%, signal=54% | |
3129 | POSITIVE REGULATION OF SMOOTH MUSCLE CONTRACTION | 6 | -0.28 | -0.60 | 0.941 | 0.978 | 1.000 | 1395 | tags=17%, list=7%, signal=18% | |
3130 | NEGATIVE REGULATION OF ANTIGEN RECEPTOR-MEDIATED SIGNALING PATHWAY | 11 | -0.25 | -0.60 | 0.958 | 0.979 | 1.000 | 5854 | tags=36%, list=28%, signal=51% | |
3131 | NEGATIVE REGULATION OF JNK CASCADE | 23 | -0.20 | -0.60 | 0.964 | 0.978 | 1.000 | 5138 | tags=26%, list=25%, signal=35% | |
3132 | VENTRICULAR CARDIAC MUSCLE CELL ACTION POTENTIAL | 13 | -0.23 | -0.60 | 0.910 | 0.978 | 1.000 | 3843 | tags=23%, list=19%, signal=28% | |
3133 | POSITIVE REGULATION BY HOST OF VIRAL GENOME REPLICATION | 5 | -0.30 | -0.60 | 0.933 | 0.978 | 1.000 | 5944 | tags=40%, list=29%, signal=56% | |
3134 | CARBOHYDRATE HOMEOSTASIS | 70 | -0.15 | -0.60 | 0.996 | 0.979 | 1.000 | 7166 | tags=33%, list=35%, signal=50% | |
3135 | GLUCOSE HOMEOSTASIS | 70 | -0.15 | -0.60 | 0.996 | 0.979 | 1.000 | 7166 | tags=33%, list=35%, signal=50% | |
3136 | DOPAMINE RECEPTOR SIGNALING PATHWAY | 11 | -0.23 | -0.60 | 0.920 | 0.980 | 1.000 | 8976 | tags=55%, list=44%, signal=97% | |
3137 | SPONGIOTROPHOBLAST LAYER DEVELOPMENT | 13 | -0.23 | -0.60 | 0.944 | 0.980 | 1.000 | 3580 | tags=23%, list=17%, signal=28% | |
3138 | ENERGY HOMEOSTASIS | 5 | -0.30 | -0.59 | 0.925 | 0.980 | 1.000 | 2509 | tags=20%, list=12%, signal=23% | |
3139 | REGULATION OF CYTOKINE PRODUCTION INVOLVED IN INFLAMMATORY RESPONSE | 10 | -0.24 | -0.59 | 0.944 | 0.981 | 1.000 | 4896 | tags=30%, list=24%, signal=39% | |
3140 | REGULATION OF P38MAPK CASCADE | 15 | -0.20 | -0.59 | 0.990 | 0.980 | 1.000 | 7364 | tags=40%, list=36%, signal=62% | |
3141 | NEGATIVE REGULATION OF ADENYLATE CYCLASE ACTIVITY | 16 | -0.21 | -0.59 | 0.958 | 0.980 | 1.000 | 3494 | tags=25%, list=17%, signal=30% | |
3142 | NEGATIVE REGULATION OF RELEASE OF SEQUESTERED CALCIUM ION INTO CYTOSOL | 9 | -0.24 | -0.59 | 0.940 | 0.980 | 1.000 | 2053 | tags=11%, list=10%, signal=12% | |
3143 | NEGATIVE REGULATION OF RYANODINE-SENSITIVE CALCIUM-RELEASE CHANNEL ACTIVITY | 9 | -0.24 | -0.59 | 0.940 | 0.980 | 1.000 | 2053 | tags=11%, list=10%, signal=12% | |
3144 | RNA MODIFICATION | 43 | -0.20 | -0.59 | 0.903 | 0.980 | 1.000 | 1304 | tags=9%, list=6%, signal=10% | |
3145 | REGULATION OF ANOIKIS | 20 | -0.20 | -0.59 | 0.954 | 0.980 | 1.000 | 57 | tags=5%, list=0%, signal=5% | |
3146 | HEME METABOLIC PROCESS | 20 | -0.22 | -0.59 | 0.921 | 0.980 | 1.000 | 2329 | tags=15%, list=11%, signal=17% | |
3147 | ECTODERMAL CELL DIFFERENTIATION | 6 | -0.28 | -0.59 | 0.955 | 0.982 | 1.000 | 5555 | tags=50%, list=27%, signal=68% | |
3148 | REGULATION OF DEVELOPMENT, HETEROCHRONIC | 6 | -0.28 | -0.59 | 0.924 | 0.982 | 1.000 | 2748 | tags=17%, list=13%, signal=19% | |
3149 | REGULATION OF TIMING OF CELL DIFFERENTIATION | 6 | -0.28 | -0.59 | 0.924 | 0.982 | 1.000 | 2748 | tags=17%, list=13%, signal=19% | |
3150 | POLYSACCHARIDE CATABOLIC PROCESS | 16 | -0.21 | -0.58 | 0.939 | 0.983 | 1.000 | 8256 | tags=44%, list=40%, signal=73% | |
3151 | GLYCOGEN CATABOLIC PROCESS | 16 | -0.21 | -0.58 | 0.939 | 0.982 | 1.000 | 8256 | tags=44%, list=40%, signal=73% | |
3152 | GLUCAN CATABOLIC PROCESS | 16 | -0.21 | -0.58 | 0.939 | 0.982 | 1.000 | 8256 | tags=44%, list=40%, signal=73% | |
3153 | CELLULAR POLYSACCHARIDE CATABOLIC PROCESS | 16 | -0.21 | -0.58 | 0.939 | 0.982 | 1.000 | 8256 | tags=44%, list=40%, signal=73% | |
3154 | POSITIVE REGULATION OF POTASSIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY | 13 | -0.21 | -0.58 | 0.945 | 0.982 | 1.000 | 5264 | tags=31%, list=26%, signal=41% | |
3155 | CELLULAR LACTAM METABOLIC PROCESS | 5 | -0.30 | -0.58 | 0.906 | 0.982 | 1.000 | 4902 | tags=40%, list=24%, signal=52% | |
3156 | POSITIVE REGULATION OF LIPOPOLYSACCHARIDE-MEDIATED SIGNALING PATHWAY | 5 | -0.30 | -0.58 | 0.941 | 0.982 | 1.000 | 5157 | tags=40%, list=25%, signal=53% | |
3157 | OUTER EAR MORPHOGENESIS | 10 | -0.22 | -0.58 | 0.950 | 0.983 | 1.000 | 4559 | tags=30%, list=22%, signal=39% | |
3158 | CEREBRAL CORTEX RADIAL GLIA GUIDED MIGRATION | 17 | -0.20 | -0.58 | 0.978 | 0.983 | 1.000 | 3650 | tags=18%, list=18%, signal=21% | |
3159 | TELENCEPHALON GLIAL CELL MIGRATION | 17 | -0.20 | -0.58 | 0.978 | 0.982 | 1.000 | 3650 | tags=18%, list=18%, signal=21% | |
3160 | NEGATIVE REGULATION OF FATTY ACID TRANSPORT | 7 | -0.28 | -0.58 | 0.930 | 0.982 | 1.000 | 1043 | tags=14%, list=5%, signal=15% | |
3161 | NCRNA PROCESSING | 146 | -0.18 | -0.58 | 0.862 | 0.982 | 1.000 | 5129 | tags=24%, list=25%, signal=32% | |
3162 | PEPTIDE CATABOLIC PROCESS | 9 | -0.25 | -0.57 | 0.939 | 0.986 | 1.000 | 2995 | tags=22%, list=15%, signal=26% | |
3163 | MEMBRANE RAFT ASSEMBLY | 10 | -0.25 | -0.57 | 0.938 | 0.986 | 1.000 | 3560 | tags=20%, list=17%, signal=24% | |
3164 | REGULATION OF FATTY ACID TRANSPORT | 13 | -0.23 | -0.57 | 0.954 | 0.987 | 1.000 | 5990 | tags=31%, list=29%, signal=43% | |
3165 | POSITIVE REGULATION OF NEURON DEATH | 22 | -0.18 | -0.57 | 0.972 | 0.988 | 1.000 | 5056 | tags=23%, list=25%, signal=30% | |
3166 | TRNA PROCESSING | 82 | -0.20 | -0.57 | 0.912 | 0.988 | 1.000 | 1532 | tags=12%, list=7%, signal=13% | |
3167 | GROWTH PLATE CARTILAGE CHONDROCYTE DIFFERENTIATION | 5 | -0.27 | -0.56 | 0.941 | 0.987 | 1.000 | 14967 | tags=100%, list=73%, signal=365% | |
3168 | PROTEIN LOCALIZATION TO MEMBRANE RAFT | 6 | -0.27 | -0.56 | 0.949 | 0.987 | 1.000 | 3560 | tags=33%, list=17%, signal=40% | |
3169 | POSITIVE REGULATION OF MULTICELLULAR ORGANISM GROWTH | 6 | -0.27 | -0.56 | 0.954 | 0.988 | 1.000 | 4902 | tags=33%, list=24%, signal=44% | |
3170 | REGULATION OF FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 11 | -0.20 | -0.56 | 0.978 | 0.989 | 1.000 | 5990 | tags=36%, list=29%, signal=51% | |
3171 | POSITIVE REGULATION OF B CELL DIFFERENTIATION | 5 | -0.27 | -0.56 | 0.950 | 0.988 | 1.000 | 1716 | tags=20%, list=8%, signal=22% | |
3172 | REGULATION OF AUDITORY RECEPTOR CELL DIFFERENTIATION | 8 | -0.25 | -0.56 | 0.935 | 0.989 | 1.000 | 4982 | tags=25%, list=24%, signal=33% | |
3173 | REGULATION OF MECHANORECEPTOR DIFFERENTIATION | 8 | -0.25 | -0.56 | 0.935 | 0.989 | 1.000 | 4982 | tags=25%, list=24%, signal=33% | |
3174 | REGULATION OF INNER EAR RECEPTOR CELL DIFFERENTIATION | 8 | -0.25 | -0.56 | 0.935 | 0.988 | 1.000 | 4982 | tags=25%, list=24%, signal=33% | |
3175 | REGULATION OF HYALURONAN BIOSYNTHETIC PROCESS | 6 | -0.28 | -0.56 | 0.940 | 0.989 | 1.000 | 5650 | tags=33%, list=27%, signal=46% | |
3176 | GLOMERULAR FILTRATION | 5 | -0.26 | -0.55 | 0.962 | 0.989 | 1.000 | 3431 | tags=20%, list=17%, signal=24% | |
3177 | PROTEIN KINASE B SIGNALING | 18 | -0.21 | -0.55 | 0.980 | 0.990 | 1.000 | 2389 | tags=17%, list=12%, signal=19% | |
3178 | REGULATION OF BETA-AMYLOID FORMATION | 7 | -0.25 | -0.55 | 0.964 | 0.990 | 1.000 | 15518 | tags=100%, list=75%, signal=405% | |
3179 | REGULATION OF SYNCYTIUM FORMATION BY PLASMA MEMBRANE FUSION | 11 | -0.23 | -0.55 | 0.924 | 0.990 | 1.000 | 7577 | tags=45%, list=37%, signal=72% | |
3180 | POSITIVE REGULATION OF HISTONE METHYLATION | 20 | -0.20 | -0.55 | 0.989 | 0.989 | 1.000 | 5743 | tags=35%, list=28%, signal=48% | |
3181 | POSITIVE REGULATION OF LAMELLIPODIUM ORGANIZATION | 15 | -0.21 | -0.55 | 0.966 | 0.989 | 1.000 | 6090 | tags=33%, list=30%, signal=47% | |
3182 | COTRANSLATIONAL PROTEIN TARGETING TO MEMBRANE | 100 | -0.18 | -0.55 | 0.808 | 0.989 | 1.000 | 10452 | tags=63%, list=51%, signal=127% | |
3183 | SRP-DEPENDENT COTRANSLATIONAL PROTEIN TARGETING TO MEMBRANE | 100 | -0.18 | -0.55 | 0.808 | 0.989 | 1.000 | 10452 | tags=63%, list=51%, signal=127% | |
3184 | REGULATION OF MITOTIC CELL CYCLE SPINDLE ASSEMBLY CHECKPOINT | 9 | -0.26 | -0.55 | 0.961 | 0.989 | 1.000 | 2662 | tags=22%, list=13%, signal=26% | |
3185 | REGULATION OF MITOTIC SPINDLE CHECKPOINT | 9 | -0.26 | -0.55 | 0.961 | 0.989 | 1.000 | 2662 | tags=22%, list=13%, signal=26% | |
3186 | NEUTROPHIL MIGRATION | 23 | -0.19 | -0.55 | 0.953 | 0.989 | 1.000 | 6876 | tags=30%, list=33%, signal=46% | |
3187 | VIRAL TRANSCRIPTION | 103 | -0.16 | -0.55 | 0.827 | 0.990 | 1.000 | 9766 | tags=52%, list=47%, signal=99% | |
3188 | NEGATIVE REGULATION OF PLATELET AGGREGATION | 6 | -0.25 | -0.54 | 0.963 | 0.990 | 1.000 | 8471 | tags=67%, list=41%, signal=113% | |
3189 | REGULATION OF T-HELPER 17 CELL DIFFERENTIATION | 5 | -0.27 | -0.54 | 0.960 | 0.990 | 1.000 | 7793 | tags=60%, list=38%, signal=96% | |
3190 | GRANULOCYTE MIGRATION | 30 | -0.18 | -0.54 | 0.976 | 0.990 | 1.000 | 6876 | tags=27%, list=33%, signal=40% | |
3191 | POSITIVE REGULATION OF P38MAPK CASCADE | 10 | -0.22 | -0.54 | 0.979 | 0.990 | 1.000 | 5157 | tags=30%, list=25%, signal=40% | |
3192 | REGULATION OF GLYCOGEN (STARCH) SYNTHASE ACTIVITY | 5 | -0.27 | -0.54 | 0.953 | 0.990 | 1.000 | 2622 | tags=20%, list=13%, signal=23% | |
3193 | RIBOSOME BIOGENESIS | 59 | -0.19 | -0.54 | 0.892 | 0.990 | 1.000 | 9224 | tags=53%, list=45%, signal=95% | |
3194 | REGULATION OF GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR PRODUCTION | 11 | -0.20 | -0.54 | 0.984 | 0.990 | 1.000 | 5558 | tags=27%, list=27%, signal=37% | |
3195 | INDOLALKYLAMINE METABOLIC PROCESS | 13 | -0.20 | -0.54 | 0.959 | 0.991 | 1.000 | 2542 | tags=15%, list=12%, signal=18% | |
3196 | NEGATIVE REGULATION OF OSTEOBLAST DIFFERENTIATION | 18 | -0.17 | -0.54 | 0.986 | 0.990 | 1.000 | 6504 | tags=33%, list=32%, signal=49% | |
3197 | RESPONSE TO COLD | 10 | -0.22 | -0.54 | 0.982 | 0.990 | 1.000 | 903 | tags=10%, list=4%, signal=10% | |
3198 | VISUAL BEHAVIOR | 12 | -0.19 | -0.54 | 0.984 | 0.990 | 1.000 | 9352 | tags=58%, list=45%, signal=107% | |
3199 | REGULATION OF CARDIAC MUSCLE CONTRACTION BY REGULATION OF THE RELEASE OF SEQUESTERED CALCIUM ION | 12 | -0.19 | -0.53 | 0.980 | 0.991 | 1.000 | 7516 | tags=50%, list=36%, signal=79% | |
3200 | NEGATIVE REGULATION OF PEPTIDYL-SERINE PHOSPHORYLATION | 15 | -0.19 | -0.53 | 0.982 | 0.991 | 1.000 | 5492 | tags=27%, list=27%, signal=36% | |
3201 | REGULATION OF CATION CHANNEL ACTIVITY | 61 | -0.13 | -0.53 | 0.996 | 0.991 | 1.000 | 7110 | tags=33%, list=35%, signal=50% | |
3202 | NEUTROPHIL CHEMOTAXIS | 21 | -0.19 | -0.53 | 0.963 | 0.992 | 1.000 | 3192 | tags=14%, list=15%, signal=17% | |
3203 | SPERMATID NUCLEUS DIFFERENTIATION | 19 | -0.16 | -0.53 | 0.996 | 0.992 | 1.000 | 3489 | tags=16%, list=17%, signal=19% | |
3204 | POSITIVE REGULATION OF OSTEOCLAST DIFFERENTIATION | 10 | -0.20 | -0.53 | 0.970 | 0.992 | 1.000 | 9381 | tags=60%, list=46%, signal=110% | |
3205 | BONE RESORPTION | 7 | -0.25 | -0.53 | 0.967 | 0.992 | 1.000 | 15369 | tags=100%, list=75%, signal=393% | |
3206 | REGULATION OF CYCLIN-DEPENDENT PROTEIN SERINE/THREONINE KINASE ACTIVITY INVOLVED IN G1/S TRANSITION OF MITOTIC CELL CYCLE | 8 | -0.22 | -0.52 | 0.988 | 0.992 | 1.000 | 6924 | tags=50%, list=34%, signal=75% | |
3207 | PROTEIN TARGETING TO ER | 102 | -0.16 | -0.52 | 0.829 | 0.992 | 1.000 | 10452 | tags=63%, list=51%, signal=127% | |
3208 | CONTRACTILE ACTIN FILAMENT BUNDLE ASSEMBLY | 9 | -0.22 | -0.52 | 0.969 | 0.992 | 1.000 | 6177 | tags=22%, list=30%, signal=32% | |
3209 | STRESS FIBER ASSEMBLY | 9 | -0.22 | -0.52 | 0.969 | 0.991 | 1.000 | 6177 | tags=22%, list=30%, signal=32% | |
3210 | CARDIAC EPITHELIAL TO MESENCHYMAL TRANSITION | 23 | -0.17 | -0.52 | 0.988 | 0.992 | 1.000 | 2252 | tags=9%, list=11%, signal=10% | |
3211 | GLUTAMINE METABOLIC PROCESS | 7 | -0.24 | -0.52 | 0.975 | 0.992 | 1.000 | 4624 | tags=29%, list=22%, signal=37% | |
3212 | RENAL FILTRATION | 6 | -0.22 | -0.52 | 0.982 | 0.992 | 1.000 | 3431 | tags=17%, list=17%, signal=20% | |
3213 | PERIPHERAL NERVOUS SYSTEM MYELIN MAINTENANCE | 8 | -0.21 | -0.51 | 0.987 | 0.993 | 1.000 | 16233 | tags=100%, list=79%, signal=471% | |
3214 | C21-STEROID HORMONE BIOSYNTHETIC PROCESS | 13 | -0.20 | -0.51 | 0.974 | 0.993 | 1.000 | 6059 | tags=38%, list=29%, signal=54% | |
3215 | POSITIVE REGULATION OF PROTEIN PROCESSING | 11 | -0.21 | -0.51 | 0.971 | 0.994 | 1.000 | 3393 | tags=18%, list=16%, signal=22% | |
3216 | REGULATION OF ATRIAL CARDIAC MUSCLE CELL MEMBRANE DEPOLARIZATION | 6 | -0.26 | -0.51 | 0.981 | 0.994 | 1.000 | 5035 | tags=33%, list=24%, signal=44% | |
3217 | NEGATIVE REGULATION OF CATENIN IMPORT INTO NUCLEUS | 9 | -0.21 | -0.51 | 0.983 | 0.994 | 1.000 | 9273 | tags=67%, list=45%, signal=121% | |
3218 | NEUROTRANSMITTER METABOLIC PROCESS | 14 | -0.18 | -0.50 | 0.975 | 0.996 | 1.000 | 7558 | tags=43%, list=37%, signal=68% | |
3219 | NEGATIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 17 | -0.16 | -0.50 | 0.986 | 0.996 | 1.000 | 4010 | tags=18%, list=19%, signal=22% | |
3220 | GRANULOCYTE CHEMOTAXIS | 28 | -0.16 | -0.50 | 0.994 | 0.996 | 1.000 | 6876 | tags=25%, list=33%, signal=37% | |
3221 | SPERM CHROMATIN CONDENSATION | 9 | -0.19 | -0.50 | 0.992 | 0.995 | 1.000 | 16734 | tags=100%, list=81%, signal=532% | |
3222 | VIRAL GENE EXPRESSION | 114 | -0.14 | -0.49 | 0.909 | 0.995 | 1.000 | 9766 | tags=50%, list=47%, signal=95% | |
3223 | MULTI-ORGANISM METABOLIC PROCESS | 115 | -0.14 | -0.49 | 0.893 | 0.995 | 1.000 | 9766 | tags=50%, list=47%, signal=94% | |
3224 | PROTEIN LOCALIZATION TO ENDOPLASMIC RETICULUM | 116 | -0.14 | -0.49 | 0.859 | 0.995 | 1.000 | 9766 | tags=53%, list=47%, signal=101% | |
3225 | GLYCEROL TRANSPORT | 5 | -0.23 | -0.49 | 0.988 | 0.995 | 1.000 | 15794 | tags=100%, list=77%, signal=428% | |
3226 | REGULATION OF CHOLESTEROL EFFLUX | 16 | -0.19 | -0.49 | 0.992 | 0.996 | 1.000 | 6685 | tags=38%, list=32%, signal=55% | |
3227 | CEREBELLAR PURKINJE CELL LAYER MORPHOGENESIS | 15 | -0.18 | -0.49 | 0.980 | 0.996 | 1.000 | 3356 | tags=13%, list=16%, signal=16% | |
3228 | SENSORY PERCEPTION OF PAIN | 17 | -0.17 | -0.48 | 0.988 | 0.997 | 1.000 | 529 | tags=6%, list=3%, signal=6% | |
3229 | REGULATION OF ANTIGEN PROCESSING AND PRESENTATION | 13 | -0.19 | -0.48 | 0.992 | 0.997 | 1.000 | 5990 | tags=31%, list=29%, signal=43% | |
3230 | POSITIVE REGULATION OF PROTEIN MATURATION | 12 | -0.20 | -0.47 | 0.983 | 0.997 | 1.000 | 3393 | tags=17%, list=16%, signal=20% | |
3231 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO ENDOPLASMIC RETICULUM | 106 | -0.14 | -0.46 | 0.881 | 0.999 | 1.000 | 9766 | tags=53%, list=47%, signal=100% | |
3232 | HUMORAL IMMUNE RESPONSE MEDIATED BY CIRCULATING IMMUNOGLOBULIN | 10 | -0.23 | -0.46 | 0.986 | 0.999 | 1.000 | 7717 | tags=50%, list=37%, signal=80% | |
3233 | REGULATION OF AMYLOID PRECURSOR PROTEIN CATABOLIC PROCESS | 9 | -0.20 | -0.45 | 0.992 | 0.999 | 1.000 | 16536 | tags=100%, list=80%, signal=506% | |
3234 | REGULATION OF SPINDLE CHECKPOINT | 12 | -0.19 | -0.45 | 0.998 | 0.999 | 1.000 | 2662 | tags=17%, list=13%, signal=19% | |
3235 | CHOLESTEROL BIOSYNTHETIC PROCESS | 25 | -0.15 | -0.45 | 0.996 | 0.999 | 1.000 | 1597 | tags=8%, list=8%, signal=9% | |
3236 | SECONDARY ALCOHOL BIOSYNTHETIC PROCESS | 25 | -0.15 | -0.45 | 0.996 | 0.999 | 1.000 | 1597 | tags=8%, list=8%, signal=9% | |
3237 | REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 19 | -0.14 | -0.45 | 0.990 | 0.999 | 1.000 | 4010 | tags=16%, list=19%, signal=20% | |
3238 | NEGATIVE REGULATION OF STRIATED MUSCLE CONTRACTION | 5 | -0.23 | -0.44 | 0.996 | 0.999 | 1.000 | 15895 | tags=100%, list=77%, signal=437% | |
3239 | CEREBELLAR PURKINJE CELL LAYER FORMATION | 12 | -0.17 | -0.44 | 1.000 | 0.999 | 1.000 | 7826 | tags=33%, list=38%, signal=54% | |
3240 | POSITIVE REGULATION OF SKELETAL MUSCLE TISSUE DEVELOPMENT | 10 | -0.16 | -0.43 | 0.998 | 0.999 | 1.000 | 7577 | tags=40%, list=37%, signal=63% | |
3241 | RETINAL ROD CELL DEVELOPMENT | 11 | -0.16 | -0.43 | 0.994 | 0.999 | 1.000 | 5351 | tags=27%, list=26%, signal=37% | |
3242 | NEGATIVE REGULATION OF AMYLOID PRECURSOR PROTEIN CATABOLIC PROCESS | 7 | -0.20 | -0.42 | 1.000 | 0.999 | 1.000 | 16536 | tags=100%, list=80%, signal=506% | |
3243 | ACTIVATION OF NF-KAPPAB-INDUCING KINASE ACTIVITY | 10 | -0.16 | -0.42 | 0.998 | 0.999 | 1.000 | 4841 | tags=20%, list=23%, signal=26% | |
3244 | NEGATIVE REGULATION OF PRI-MIRNA TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 5 | -0.19 | -0.42 | 0.998 | 0.999 | 1.000 | 10036 | tags=80%, list=49%, signal=156% | |
3245 | NUCLEAR-TRANSCRIBED MRNA CATABOLIC PROCESS, NONSENSE-MEDIATED DECAY | 101 | -0.12 | -0.42 | 0.930 | 0.999 | 1.000 | 9861 | tags=51%, list=48%, signal=98% | |
3246 | REGULATION OF MICROVILLUS ORGANIZATION | 5 | -0.20 | -0.42 | 1.000 | 0.999 | 1.000 | 3705 | tags=20%, list=18%, signal=24% | |
3247 | REGULATION OF MICROVILLUS ASSEMBLY | 5 | -0.20 | -0.42 | 1.000 | 0.998 | 1.000 | 3705 | tags=20%, list=18%, signal=24% | |
3248 | MEMBRANE RAFT ORGANIZATION | 15 | -0.14 | -0.39 | 1.000 | 1.000 | 1.000 | 8170 | tags=47%, list=40%, signal=77% | |
3249 | POSITIVE REGULATION OF LIPID TRANSPORT | 30 | -0.12 | -0.37 | 1.000 | 1.000 | 1.000 | 6961 | tags=33%, list=34%, signal=50% | |
3250 | NEGATIVE REGULATION OF INTERLEUKIN-6 PRODUCTION | 18 | -0.12 | -0.33 | 1.000 | 1.000 | 1.000 | 18053 | tags=100%, list=88%, signal=806% |