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 | HUMANCYC_SUPERPATHWAY OF GLYCOLYSIS, PYRUVATE DEHYDROGENASE, TCA, AND GLYOXYLATE BYPASS | Details ... | 39 | 0.83 | 1.68 | 0.000 | 0.043 | 0.045 | 661 | tags=31%, list=4%, signal=32% |
2 | REACTOME_METABOLISM_OF_PROTEINS | Details ... | 98 | 0.73 | 1.66 | 0.000 | 0.043 | 0.091 | 2132 | tags=32%, list=11%, signal=36% |
3 | REACTOME_METABOLISM_OF_CARBOHYDRATES | Details ... | 70 | 0.75 | 1.66 | 0.000 | 0.030 | 0.096 | 1626 | tags=26%, list=9%, signal=28% |
4 | REACTOME_FORMATION_OF_FIBRIN_CLOT__CLOTTING_CASCADE_ | Details ... | 28 | 0.85 | 1.65 | 0.002 | 0.030 | 0.130 | 1450 | tags=14%, list=8%, signal=15% |
5 | REACTOME_L13A_MEDIATED_TRANSLATIONAL_SILENCING_OF_CERULOPLASMIN_EXPRESSION | Details ... | 52 | 0.78 | 1.65 | 0.000 | 0.026 | 0.137 | 1911 | tags=23%, list=10%, signal=26% |
6 | HUMANCYC_SUPERPATHWAY OF N-ACETYLNEURAMINATE DEGRADATION | Details ... | 22 | 0.89 | 1.65 | 0.000 | 0.021 | 0.137 | 661 | tags=41%, list=4%, signal=42% |
7 | HUMANCYC_SUPERPATHWAY OF GLYCOLYSIS AND ENTNER-DOUDOROFF | Details ... | 22 | 0.87 | 1.64 | 0.000 | 0.020 | 0.148 | 1626 | tags=59%, list=9%, signal=65% |
8 | REACTOME__3___UTR_MEDIATED_TRANSLATIONAL_REGULATION | Details ... | 52 | 0.78 | 1.64 | 0.000 | 0.021 | 0.179 | 1911 | tags=23%, list=10%, signal=26% |
9 | HUMANCYC_GLYCOLYSIS III | Details ... | 21 | 0.90 | 1.63 | 0.002 | 0.025 | 0.233 | 661 | tags=48%, list=4%, signal=49% |
10 | REACTOME_DIABETES_PATHWAYS | Details ... | 159 | 0.66 | 1.62 | 0.000 | 0.029 | 0.276 | 2925 | tags=38%, list=16%, signal=45% |
11 | REACTOME_EXOCYTOSIS_OF_ALPHA_GRANULE_ | Details ... | 40 | 0.80 | 1.62 | 0.005 | 0.029 | 0.306 | 1450 | tags=15%, list=8%, signal=16% |
12 | HUMANCYC_GLYCOLYSIS I | Details ... | 20 | 0.90 | 1.61 | 0.002 | 0.028 | 0.321 | 661 | tags=50%, list=4%, signal=52% |
13 | REACTOME_EUKARYOTIC_TRANSLATION_ELONGATION | Details ... | 47 | 0.77 | 1.60 | 0.002 | 0.036 | 0.400 | 1859 | tags=19%, list=10%, signal=21% |
14 | HUMANCYC_GLYCOLYSIS V | Details ... | 18 | 0.90 | 1.60 | 0.004 | 0.037 | 0.425 | 661 | tags=50%, list=4%, signal=52% |
15 | REACTOME_EUKARYOTIC_TRANSLATION_TERMINATION | Details ... | 46 | 0.76 | 1.59 | 0.002 | 0.045 | 0.527 | 1978 | tags=20%, list=11%, signal=22% |
16 | REACTOME_PEPTIDE_CHAIN_ELONGATION | Details ... | 45 | 0.77 | 1.58 | 0.002 | 0.047 | 0.567 | 1859 | tags=18%, list=10%, signal=20% |
17 | REACTOME_GTP_HYDROLYSIS_AND_JOINING_OF_THE_60S_RIBOSOMAL_SUBUNIT | Details ... | 53 | 0.75 | 1.58 | 0.003 | 0.047 | 0.581 | 1911 | tags=21%, list=10%, signal=23% |
18 | REACTOME_GLUCOSE_METABOLISM | Details ... | 54 | 0.74 | 1.58 | 0.003 | 0.052 | 0.631 | 2317 | tags=28%, list=12%, signal=32% |
19 | REACTOME_TRANSLATION | Details ... | 63 | 0.72 | 1.57 | 0.003 | 0.052 | 0.656 | 1978 | tags=27%, list=11%, signal=30% |
20 | REACTOME_FORMATION_OF_A_POOL_OF_FREE_40S_SUBUNITS | Details ... | 44 | 0.77 | 1.57 | 0.003 | 0.051 | 0.661 | 1859 | tags=18%, list=10%, signal=20% |
21 | REACTOME_EUKARYOTIC_TRANSLATION_INITIATION | 58 | 0.73 | 1.57 | 0.002 | 0.050 | 0.676 | 1911 | tags=26%, list=10%, signal=29% | |
22 | REACTOME_VIRAL_MRNA_TRANSLATION | 46 | 0.75 | 1.56 | 0.005 | 0.055 | 0.734 | 1859 | tags=17%, list=10%, signal=19% | |
23 | REACTOME_INTRINSIC_PATHWAY | 16 | 0.90 | 1.56 | 0.002 | 0.054 | 0.741 | 1450 | tags=25%, list=8%, signal=27% | |
24 | HUMANCYC_GLUCONEOGENESIS | 17 | 0.88 | 1.56 | 0.004 | 0.058 | 0.788 | 1480 | tags=47%, list=8%, signal=51% | |
25 | REACTOME_COMPLEMENT_CASCADE | 14 | 0.93 | 1.55 | 0.004 | 0.058 | 0.805 | 826 | tags=36%, list=4%, signal=37% | |
26 | REACTOME_CAP_DEPENDENT_TRANSLATION_INITIATION | 58 | 0.73 | 1.55 | 0.002 | 0.059 | 0.822 | 1911 | tags=26%, list=10%, signal=29% | |
27 | NCI_SIGNALING EVENTS MEDIATED BY HDAC CLASS III | 30 | 0.82 | 1.55 | 0.002 | 0.057 | 0.824 | 880 | tags=47%, list=5%, signal=49% | |
28 | REACTOME_PLATELET_DEGRANULATION_ | 42 | 0.75 | 1.54 | 0.004 | 0.064 | 0.871 | 1450 | tags=17%, list=8%, signal=18% | |
29 | REACTOME_INSULIN_SYNTHESIS_AND_SECRETION | 66 | 0.71 | 1.54 | 0.005 | 0.066 | 0.890 | 2015 | tags=20%, list=11%, signal=22% | |
30 | REACTOME_INFLUENZA_VIRAL_RNA_TRANSCRIPTION_AND_REPLICATION | 90 | 0.68 | 1.54 | 0.003 | 0.065 | 0.895 | 1972 | tags=26%, list=11%, signal=28% | |
31 | REACTOME_LIPOPROTEIN_METABOLISM | 18 | 0.86 | 1.52 | 0.006 | 0.100 | 0.967 | 1291 | tags=22%, list=7%, signal=24% | |
32 | REACTOME_BIOLOGICAL_OXIDATIONS | 46 | 0.72 | 1.50 | 0.010 | 0.130 | 0.991 | 2301 | tags=15%, list=12%, signal=17% | |
33 | REACTOME_GLUCONEOGENESIS | 11 | 0.91 | 1.50 | 0.004 | 0.131 | 0.992 | 1426 | tags=64%, list=8%, signal=69% | |
34 | REACTOME_INFLUENZA_LIFE_CYCLE | 111 | 0.64 | 1.49 | 0.001 | 0.137 | 0.998 | 2317 | tags=24%, list=12%, signal=28% | |
35 | REACTOME_RESPONSE_TO_ELEVATED_PLATELET_CYTOSOLIC_CA__ | 44 | 0.72 | 1.49 | 0.016 | 0.141 | 0.998 | 1450 | tags=16%, list=8%, signal=17% | |
36 | REACTOME_INITIAL_TRIGGERING_OF_COMPLEMENT | 10 | 0.94 | 1.48 | 0.009 | 0.155 | 0.999 | 826 | tags=50%, list=4%, signal=52% | |
37 | BIOCARTA_CLASSICAL COMPLEMENT PATHWAY | 10 | 0.94 | 1.48 | 0.002 | 0.158 | 1.000 | 826 | tags=50%, list=4%, signal=52% | |
38 | REACTOME_COMMON_PATHWAY | 11 | 0.92 | 1.48 | 0.015 | 0.155 | 1.000 | 972 | tags=18%, list=5%, signal=19% | |
39 | REACTOME_INFLUENZA_INFECTION | 115 | 0.63 | 1.48 | 0.006 | 0.158 | 1.000 | 2347 | tags=26%, list=13%, signal=30% | |
40 | REACTOME_METABOLISM_OF_NUCLEOTIDES | 62 | 0.67 | 1.46 | 0.026 | 0.184 | 1.000 | 2471 | tags=47%, list=13%, signal=54% | |
41 | REACTOME_REGULATION_OF_BETA_CELL_DEVELOPMENT | 16 | 0.85 | 1.46 | 0.015 | 0.199 | 1.000 | 891 | tags=13%, list=5%, signal=13% | |
42 | REACTOME_PURINE_METABOLISM | 39 | 0.72 | 1.45 | 0.032 | 0.230 | 1.000 | 2471 | tags=51%, list=13%, signal=59% | |
43 | REACTOME_INTEGRATION_OF_ENERGY_METABOLISM | 109 | 0.62 | 1.44 | 0.008 | 0.236 | 1.000 | 2714 | tags=42%, list=15%, signal=49% | |
44 | REACTOME_PURINE_BIOSYNTHESIS | 24 | 0.78 | 1.44 | 0.034 | 0.231 | 1.000 | 2471 | tags=58%, list=13%, signal=67% | |
45 | HUMANCYC_SERINE-ISOCITRATE LYASE PATHWAY | 16 | 0.84 | 1.44 | 0.024 | 0.246 | 1.000 | 1480 | tags=50%, list=8%, signal=54% | |
46 | REACTOME_POST_TRANSLATIONAL_PROTEIN_MODIFICATION | 22 | 0.78 | 1.43 | 0.033 | 0.255 | 1.000 | 2429 | tags=32%, list=13%, signal=37% | |
47 | HUMANCYC_ENTNER-DOUDOROFF PATHWAY II (NON-PHOSPHORYLATIVE) | 12 | 0.87 | 1.43 | 0.033 | 0.251 | 1.000 | 1244 | tags=42%, list=7%, signal=45% | |
48 | HUMANCYC_TCA CYCLE VARIATION III (EUKARYOTIC) | 16 | 0.82 | 1.43 | 0.037 | 0.256 | 1.000 | 3033 | tags=63%, list=16%, signal=75% | |
49 | REACTOME_CHYLOMICRON_MEDIATED_LIPID_TRANSPORT | 14 | 0.87 | 1.43 | 0.021 | 0.253 | 1.000 | 1291 | tags=29%, list=7%, signal=31% | |
50 | HUMANCYC_SUPERPATHWAY OF HISTIDINE, PURINE, AND PYRIMIDINE BIOSYNTHESIS | 33 | 0.73 | 1.42 | 0.046 | 0.280 | 1.000 | 2471 | tags=52%, list=13%, signal=59% | |
51 | HUMANCYC_GLYCINE BETAINE DEGRADATION | 10 | 0.89 | 1.41 | 0.022 | 0.293 | 1.000 | 1531 | tags=30%, list=8%, signal=33% | |
52 | REACTOME_GENE_EXPRESSION | 145 | 0.59 | 1.41 | 0.012 | 0.296 | 1.000 | 2317 | tags=28%, list=12%, signal=31% | |
53 | REACTOME_GLUCOSE_REGULATION_OF_INSULIN_SECRETION | 90 | 0.62 | 1.40 | 0.027 | 0.328 | 1.000 | 2714 | tags=47%, list=15%, signal=54% | |
54 | REACTOME_PHASE_II_CONJUGATION | 17 | 0.81 | 1.40 | 0.046 | 0.330 | 1.000 | 1254 | tags=18%, list=7%, signal=19% | |
55 | BIOCARTA_PLATELET AMYLOID PRECURSOR PROTEIN PATHWAY | 13 | 0.83 | 1.39 | 0.068 | 0.361 | 1.000 | 1407 | tags=23%, list=8%, signal=25% | |
56 | REACTOME_METABOLISM_OF_VITAMINS_AND_COFACTORS | 19 | 0.78 | 1.38 | 0.073 | 0.400 | 1.000 | 2558 | tags=42%, list=14%, signal=49% | |
57 | BIOCARTA_ACTIVATION OF PKC THROUGH G-PROTEIN COUPLED RECEPTORS | 10 | 0.87 | 1.37 | 0.043 | 0.410 | 1.000 | 1111 | tags=20%, list=6%, signal=21% | |
58 | BIOCARTA_CARDIAC PROTECTION AGAINST ROS | 11 | 0.86 | 1.37 | 0.061 | 0.406 | 1.000 | 1333 | tags=18%, list=7%, signal=20% | |
59 | INOH_GROWTH HORMONE SIGNALING PATHWAY(JAK2 STAT5) | 10 | 0.87 | 1.37 | 0.052 | 0.422 | 1.000 | 724 | tags=10%, list=4%, signal=10% | |
60 | REACTOME_TRANSLATION_INITIATION_COMPLEX_FORMATION | 30 | 0.70 | 1.36 | 0.082 | 0.428 | 1.000 | 1911 | tags=27%, list=10%, signal=30% | |
61 | NCI_HYPOXIC AND OXYGEN HOMEOSTASIS REGULATION OF HIF-1-ALPHA | 67 | 0.62 | 1.36 | 0.052 | 0.429 | 1.000 | 1283 | tags=24%, list=7%, signal=26% | |
62 | HUMANCYC_GLUTATHIONE-MEDIATED DETOXIFICATION | 16 | 0.80 | 1.36 | 0.059 | 0.428 | 1.000 | 1322 | tags=50%, list=7%, signal=54% | |
63 | REACTOME_METABOLISM_OF_WATER_SOLUBLE_VITAMINS_AND_COFACTORS | 19 | 0.78 | 1.36 | 0.049 | 0.425 | 1.000 | 2558 | tags=42%, list=14%, signal=49% | |
64 | HUMANCYC_FATTY ACID BETA-OXIDATION II (CORE PATHWAY) | 16 | 0.78 | 1.36 | 0.085 | 0.438 | 1.000 | 2114 | tags=31%, list=11%, signal=35% | |
65 | HUMANCYC_SALVAGE PATHWAYS OF PURINE AND PYRIMIDINE NUCLEOTIDES | 19 | 0.77 | 1.35 | 0.078 | 0.437 | 1.000 | 2352 | tags=37%, list=13%, signal=42% | |
66 | HUMANCYC_PHOSPHOLIPID BIOSYNTHESIS I | 10 | 0.85 | 1.35 | 0.061 | 0.430 | 1.000 | 1648 | tags=40%, list=9%, signal=44% | |
67 | REACTOME_REGULATION_OF_INSULIN_SECRETION | 101 | 0.58 | 1.35 | 0.043 | 0.461 | 1.000 | 2714 | tags=43%, list=15%, signal=50% | |
68 | REACTOME_STRIATED_MUSCLE_CONTRACTION | 14 | 0.80 | 1.34 | 0.097 | 0.491 | 1.000 | 2895 | tags=36%, list=16%, signal=42% | |
69 | BIOCARTA_DOWNREGULATED OF MTA-3 IN ER-NEGATIVE BREAST TUMORS | 18 | 0.75 | 1.33 | 0.118 | 0.502 | 1.000 | 1591 | tags=39%, list=9%, signal=42% | |
70 | REACTOME_ATP_FORMATION | 15 | 0.78 | 1.32 | 0.117 | 0.533 | 1.000 | 2128 | tags=53%, list=11%, signal=60% | |
71 | REACTOME_NEUROTRANSMITTER_RELEASE_CYCLE | 15 | 0.76 | 1.32 | 0.111 | 0.537 | 1.000 | 1406 | tags=20%, list=8%, signal=22% | |
72 | REACTOME_CITRIC_ACID_CYCLE__TCA_CYCLE_ | 12 | 0.81 | 1.32 | 0.109 | 0.553 | 1.000 | 3124 | tags=67%, list=17%, signal=80% | |
73 | REACTOME_COOPERATION_OF_PREFOLDIN_AND_TRIC_CCT__IN_ACTIN_AND_TUBULIN_FOLDING | 10 | 0.83 | 1.31 | 0.107 | 0.560 | 1.000 | 2132 | tags=70%, list=11%, signal=79% | |
74 | HUMANCYC_SUPERPATHWAY OF GLYOXYLATE CYCLE | 10 | 0.84 | 1.31 | 0.091 | 0.564 | 1.000 | 2245 | tags=50%, list=12%, signal=57% | |
75 | REACTOME_CHAPERONIN_MEDIATED_PROTEIN_FOLDING | 10 | 0.83 | 1.30 | 0.135 | 0.623 | 1.000 | 2132 | tags=70%, list=11%, signal=79% | |
76 | HUMANCYC_DE NOVO BIOSYNTHESIS OF PYRIMIDINE RIBONUCLEOTIDES | 11 | 0.79 | 1.29 | 0.169 | 0.639 | 1.000 | 1804 | tags=73%, list=10%, signal=80% | |
77 | REACTOME_PHASE_1_FUNCTIONALIZATION | 10 | 0.81 | 1.29 | 0.149 | 0.645 | 1.000 | 2301 | tags=30%, list=12%, signal=34% | |
78 | REACTOME_GAMMA_CARBOXYLATION__TRANSPORT__AND_AMINO_TERMINAL_CLEAVAGE_OF_PROTEINS | 10 | 0.82 | 1.29 | 0.142 | 0.642 | 1.000 | 2064 | tags=30%, list=11%, signal=34% | |
79 | HUMANCYC_TCA CYCLE | 16 | 0.73 | 1.27 | 0.168 | 0.717 | 1.000 | 3033 | tags=50%, list=16%, signal=60% | |
80 | HUMANCYC_TRIACYLGLYCEROL BIOSYNTHESIS | 11 | 0.80 | 1.27 | 0.129 | 0.722 | 1.000 | 1735 | tags=27%, list=9%, signal=30% | |
81 | REACTOME_PYRUVATE_METABOLISM_AND_TCA_CYCLE | 17 | 0.72 | 1.27 | 0.179 | 0.714 | 1.000 | 3124 | tags=53%, list=17%, signal=64% | |
82 | HUMANCYC_SUPERPATHWAY OF GLYOXYLATE BYPASS AND TCA | 16 | 0.73 | 1.26 | 0.168 | 0.716 | 1.000 | 3033 | tags=50%, list=16%, signal=60% | |
83 | REACTOME_PYRIMIDINE_METABOLISM | 17 | 0.74 | 1.26 | 0.161 | 0.709 | 1.000 | 986 | tags=41%, list=5%, signal=43% | |
84 | HUMANCYC_PURINE NUCLEOTIDES DE NOVO BIOSYNTHESIS I | 25 | 0.66 | 1.26 | 0.164 | 0.725 | 1.000 | 2708 | tags=52%, list=15%, signal=61% | |
85 | REACTOME_FORMATION_OF_ATP_BY_CHEMIOSMOTIC_COUPLING | 12 | 0.79 | 1.26 | 0.165 | 0.719 | 1.000 | 2128 | tags=58%, list=11%, signal=66% | |
86 | REACTOME_CYTOSOLIC_TRNA_AMINOACYLATION | 14 | 0.73 | 1.25 | 0.182 | 0.733 | 1.000 | 3042 | tags=50%, list=16%, signal=60% | |
87 | REACTOME_MUSCLE_CONTRACTION | 25 | 0.66 | 1.25 | 0.162 | 0.727 | 1.000 | 2984 | tags=28%, list=16%, signal=33% | |
88 | REACTOME_METABOLISM_OF_AMINO_ACIDS | 106 | 0.54 | 1.25 | 0.082 | 0.718 | 1.000 | 1881 | tags=30%, list=10%, signal=33% | |
89 | REACTOME_INNATE_IMMUNITY_SIGNALING | 40 | 0.61 | 1.25 | 0.145 | 0.732 | 1.000 | 896 | tags=20%, list=5%, signal=21% | |
90 | REACTOME_PROTEIN_FOLDING | 13 | 0.75 | 1.25 | 0.203 | 0.737 | 1.000 | 2132 | tags=62%, list=11%, signal=69% | |
91 | BIOCARTA_SKELETAL MUSCLE HYPERTROPHY IS REGULATED VIA AKT-MTOR PATHWAY | 24 | 0.68 | 1.24 | 0.194 | 0.731 | 1.000 | 522 | tags=25%, list=3%, signal=26% | |
92 | NCI_HIF-1-ALPHA TRANSCRIPTION FACTOR NETWORK | 57 | 0.59 | 1.24 | 0.123 | 0.725 | 1.000 | 1283 | tags=21%, list=7%, signal=23% | |
93 | REACTOME_PHASE_1___FUNCTIONALIZATION_OF_COMPOUNDS | 29 | 0.65 | 1.24 | 0.154 | 0.751 | 1.000 | 2301 | tags=14%, list=12%, signal=16% | |
94 | BIOCARTA_INTRINSIC PROTHROMBIN ACTIVATION PATHWAY | 22 | 0.67 | 1.23 | 0.195 | 0.783 | 1.000 | 1450 | tags=18%, list=8%, signal=20% | |
95 | REACTOME_VIRAL_MESSENGER_RNA_SYNTHESIS | 43 | 0.61 | 1.22 | 0.170 | 0.804 | 1.000 | 2127 | tags=37%, list=11%, signal=42% | |
96 | REACTOME_PROCESSING_OF_CAPPED_INTRON_CONTAINING_PRE_MRNA | 85 | 0.54 | 1.22 | 0.136 | 0.810 | 1.000 | 2317 | tags=31%, list=12%, signal=35% | |
97 | REACTOME_REGULATION_OF_INSULIN_LIKE_GROWTH_FACTOR__IGF__ACTIVITY_BY_INSULIN_LIKE_GROWTH_FACTOR_BINDING_PROTEINS__IGFBPS_ | 12 | 0.76 | 1.22 | 0.209 | 0.807 | 1.000 | 113 | tags=8%, list=1%, signal=8% | |
98 | REACTOME_ABORTIVE_ELONGATION_OF_HIV_1_TRANSCRIPT_IN_THE_ABSENCE_OF_TAT | 14 | 0.72 | 1.22 | 0.244 | 0.803 | 1.000 | 3436 | tags=79%, list=18%, signal=96% | |
99 | REACTOME_DUAL_INCISION_REACTION_IN_TC_NER | 19 | 0.68 | 1.21 | 0.227 | 0.806 | 1.000 | 3413 | tags=63%, list=18%, signal=77% | |
100 | BIOCARTA_OXIDATIVE STRESS INDUCED GENE EXPRESSION VIA NRF2 | 16 | 0.69 | 1.21 | 0.238 | 0.808 | 1.000 | 1814 | tags=19%, list=10%, signal=21% | |
101 | HUMANCYC_PHOSPHOLIPID BIOSYNTHESIS II | 22 | 0.66 | 1.21 | 0.198 | 0.826 | 1.000 | 1648 | tags=23%, list=9%, signal=25% | |
102 | REACTOME_FORMATION_OF_TRANSCRIPTION_COUPLED_NER__TC_NER__REPAIR_COMPLEX | 19 | 0.68 | 1.20 | 0.217 | 0.821 | 1.000 | 3413 | tags=63%, list=18%, signal=77% | |
103 | REACTOME_RAS_ACTIVATION_UOPN_CA2__INFUX_THROUGH_NMDA_RECEPTOR | 10 | 0.75 | 1.20 | 0.257 | 0.815 | 1.000 | 3168 | tags=40%, list=17%, signal=48% | |
104 | HUMANCYC_PURINE NUCLEOTIDES DE NOVO BIOSYNTHESIS II | 10 | 0.77 | 1.20 | 0.239 | 0.809 | 1.000 | 2471 | tags=70%, list=13%, signal=81% | |
105 | REACTOME_MRNA_CAPPING | 21 | 0.67 | 1.20 | 0.238 | 0.805 | 1.000 | 3436 | tags=62%, list=18%, signal=76% | |
106 | HUMANCYC_RESPIRATION (ANAEROBIC) | 16 | 0.70 | 1.20 | 0.229 | 0.804 | 1.000 | 1242 | tags=25%, list=7%, signal=27% | |
107 | REACTOME_MRNA_SPLICING | 67 | 0.55 | 1.20 | 0.155 | 0.803 | 1.000 | 2127 | tags=33%, list=11%, signal=37% | |
108 | HUMANCYC_COLANIC ACID BUILDING BLOCKS BIOSYNTHESIS | 10 | 0.74 | 1.20 | 0.268 | 0.809 | 1.000 | 1416 | tags=40%, list=8%, signal=43% | |
109 | REACTOME_MRNA_SPLICING___MAJOR_PATHWAY | 67 | 0.55 | 1.20 | 0.157 | 0.805 | 1.000 | 2127 | tags=33%, list=11%, signal=37% | |
110 | REACTOME_MRNA_SPLICING___MINOR_PATHWAY | 28 | 0.63 | 1.20 | 0.205 | 0.799 | 1.000 | 2127 | tags=43%, list=11%, signal=48% | |
111 | REACTOME_ELONGATION_AND_PROCESSING_OF_CAPPED_TRANSCRIPTS | 86 | 0.52 | 1.19 | 0.174 | 0.826 | 1.000 | 2127 | tags=31%, list=11%, signal=35% | |
112 | REACTOME_ELECTRON_TRANSPORT_CHAIN | 53 | 0.56 | 1.18 | 0.207 | 0.850 | 1.000 | 2714 | tags=53%, list=15%, signal=62% | |
113 | REACTOME_METABOLISM_OF_MRNA | 15 | 0.70 | 1.18 | 0.284 | 0.853 | 1.000 | 2345 | tags=47%, list=13%, signal=53% | |
114 | REACTOME_TRNA_AMINOACYLATION | 18 | 0.67 | 1.17 | 0.270 | 0.865 | 1.000 | 3408 | tags=44%, list=18%, signal=54% | |
115 | REACTOME_SYNTHESIS_OF_GPI_ANCHORED_PROTEINS | 11 | 0.74 | 1.17 | 0.302 | 0.862 | 1.000 | 2429 | tags=27%, list=13%, signal=31% | |
116 | REACTOME_RNA_POL_II_CTD_PHOSPHORYLATION_AND_INTERACTION_WITH_CE | 20 | 0.66 | 1.17 | 0.256 | 0.863 | 1.000 | 3436 | tags=60%, list=18%, signal=74% | |
117 | NCI_VISUAL SIGNAL TRANSDUCTION: CONES | 18 | 0.67 | 1.17 | 0.252 | 0.857 | 1.000 | 1561 | tags=11%, list=8%, signal=12% | |
118 | REACTOME_ELONGATION_OF_INTRON_CONTAINING_TRANSCRIPTS_AND_CO_TRANSCRIPTIONAL_MRNA_SPLICING | 86 | 0.52 | 1.17 | 0.179 | 0.853 | 1.000 | 2127 | tags=31%, list=11%, signal=35% | |
119 | BIOCARTA_G-PROTEIN SIGNALING THROUGH TUBBY PROTEINS | 10 | 0.73 | 1.17 | 0.310 | 0.852 | 1.000 | 1111 | tags=20%, list=6%, signal=21% | |
120 | BIOCARTA_EPO SIGNALING PATHWAY | 11 | 0.74 | 1.17 | 0.294 | 0.845 | 1.000 | 3077 | tags=36%, list=17%, signal=44% | |
121 | REACTOME_DEADENYLATION_DEPENDENT_MRNA_DECAY | 15 | 0.70 | 1.17 | 0.278 | 0.842 | 1.000 | 2345 | tags=47%, list=13%, signal=53% | |
122 | REACTOME_FORMATION_OF_THE_HIV_1_EARLY_ELONGATION_COMPLEX | 22 | 0.63 | 1.16 | 0.253 | 0.845 | 1.000 | 3436 | tags=68%, list=18%, signal=84% | |
123 | REACTOME_RNA_POL_II_CTD_PHOSPHORYLATION_AND_INTERACTION_WITH_CE1 | 20 | 0.66 | 1.16 | 0.251 | 0.850 | 1.000 | 3436 | tags=60%, list=18%, signal=74% | |
124 | REACTOME_FORMATION_OF_THE_EARLY_ELONGATION_COMPLEX | 22 | 0.63 | 1.16 | 0.264 | 0.856 | 1.000 | 3436 | tags=68%, list=18%, signal=84% | |
125 | BIOCARTA_GRANZYME A MEDIATED APOPTOSIS PATHWAY | 12 | 0.71 | 1.16 | 0.308 | 0.855 | 1.000 | 1804 | tags=25%, list=10%, signal=28% | |
126 | INOH_HETEROTRIMERIC GTP-BINDING PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY (THROUGH_G_ALPHA_S,_CHOLERA_TOXIN,_ADENYLATE_CYCLASE_AND_CAMP) | 179 | 0.47 | 1.16 | 0.141 | 0.852 | 1.000 | 2054 | tags=7%, list=11%, signal=8% | |
127 | BIOCARTA_ERYTHROPOIETIN MEDIATED NEUROPROTECTION THROUGH NF-KB | 12 | 0.70 | 1.15 | 0.329 | 0.868 | 1.000 | 1068 | tags=25%, list=6%, signal=27% | |
128 | BIOCARTA_PHOSPHOINOSITIDES AND THEIR DOWNSTREAM TARGETS | 21 | 0.64 | 1.15 | 0.289 | 0.866 | 1.000 | 1695 | tags=33%, list=9%, signal=37% | |
129 | REACTOME_AMINO_ACID_TRANSPORT_ACROSS_THE_PLASMA_MEMBRANE | 12 | 0.70 | 1.15 | 0.328 | 0.862 | 1.000 | 403 | tags=17%, list=2%, signal=17% | |
130 | BIOCARTA_TUMOR SUPPRESSOR ARF INHIBITS RIBOSOMAL BIOGENESIS | 20 | 0.64 | 1.14 | 0.314 | 0.880 | 1.000 | 1330 | tags=30%, list=7%, signal=32% | |
131 | REACTOME_FORMATION_AND_MATURATION_OF_MRNA_TRANSCRIPT | 102 | 0.49 | 1.14 | 0.199 | 0.895 | 1.000 | 2127 | tags=26%, list=11%, signal=30% | |
132 | NCI_LPA4-MEDIATED SIGNALING EVENTS | 12 | 0.68 | 1.13 | 0.324 | 0.913 | 1.000 | 564 | tags=8%, list=3%, signal=9% | |
133 | REACTOME_RNA_POLYMERASE_I_TRANSCRIPTION | 19 | 0.62 | 1.13 | 0.294 | 0.920 | 1.000 | 2311 | tags=47%, list=12%, signal=54% | |
134 | REACTOME_MRNA_PROCESSING | 24 | 0.61 | 1.13 | 0.310 | 0.915 | 1.000 | 3436 | tags=58%, list=18%, signal=71% | |
135 | INOH_HETEROTRIMERIC GTP-BINDING PROTEIN COUPLED RECEPTOR SIGNALING PATHWAY (THROUGH G ALPHA I, ADENYLATE CYCLASE AND CAMP) | 175 | 0.45 | 1.13 | 0.182 | 0.913 | 1.000 | 2054 | tags=7%, list=11%, signal=8% | |
136 | REACTOME_ACTIVATION_OF_THE_MRNA_UPON_BINDING_OF_THE_CAP_BINDING_COMPLEX_AND_EIFS__AND_SUBSEQUENT_BINDING_TO_43S | 31 | 0.57 | 1.12 | 0.295 | 0.908 | 1.000 | 1911 | tags=26%, list=10%, signal=29% | |
137 | BIOCARTA_ROLES OF FL ARRESTIN DEPENDENT RECRUITMENT OF SRC KINASES IN GPCR SIGNALING | 32 | 0.57 | 1.12 | 0.286 | 0.923 | 1.000 | 1667 | tags=19%, list=9%, signal=21% | |
138 | BIOCARTA_CHROMATIN REMODELING BY HSWI/SNF ATP-DEPENDENT COMPLEXES | 15 | 0.65 | 1.12 | 0.366 | 0.930 | 1.000 | 1739 | tags=33%, list=9%, signal=37% | |
139 | INOH_HETEROTRIMERIC GPCR SIGNALING PATHWAY (THROUGH G ALPHA I AND PERTUSSIS TOXIN) | 175 | 0.45 | 1.12 | 0.215 | 0.924 | 1.000 | 2054 | tags=7%, list=11%, signal=8% | |
140 | BIOCARTA_RB TUMOR SUPPRESSOR/CHECKPOINT SIGNALING IN RESPONSE TO DNA DAMAGE | 12 | 0.68 | 1.11 | 0.343 | 0.922 | 1.000 | 1330 | tags=33%, list=7%, signal=36% | |
141 | REACTOME_RIBOSOMAL_SCANNING_AND_START_CODON_RECOGNITION | 30 | 0.58 | 1.11 | 0.309 | 0.919 | 1.000 | 3144 | tags=37%, list=17%, signal=44% | |
142 | REACTOME_SNRNP_ASSEMBLY | 27 | 0.57 | 1.11 | 0.323 | 0.922 | 1.000 | 2914 | tags=48%, list=16%, signal=57% | |
143 | REACTOME_P53_DEPENDENT_G1_DNA_DAMAGE_RESPONSE | 39 | 0.54 | 1.11 | 0.286 | 0.919 | 1.000 | 1881 | tags=46%, list=10%, signal=51% | |
144 | REACTOME_BASE_EXCISION_REPAIR | 14 | 0.65 | 1.11 | 0.346 | 0.914 | 1.000 | 2006 | tags=43%, list=11%, signal=48% | |
145 | REACTOME_INTEGRIN_CELL_SURFACE_INTERACTIONS | 56 | 0.51 | 1.11 | 0.267 | 0.911 | 1.000 | 2213 | tags=13%, list=12%, signal=14% | |
146 | BIOCARTA_HYPOXIA AND P53 IN THE CARDIOVASCULAR SYSTEM | 16 | 0.64 | 1.11 | 0.349 | 0.906 | 1.000 | 896 | tags=25%, list=5%, signal=26% | |
147 | REACTOME_ORNITHINE_METABOLISM | 43 | 0.55 | 1.10 | 0.295 | 0.922 | 1.000 | 1881 | tags=42%, list=10%, signal=46% | |
148 | BIOCARTA_IL 3 SIGNALING PATHWAY | 11 | 0.69 | 1.10 | 0.374 | 0.918 | 1.000 | 3077 | tags=36%, list=17%, signal=44% | |
149 | INOH_WNT SECRETORY PATHWAY (MAMMAL) | 48 | 0.52 | 1.10 | 0.306 | 0.924 | 1.000 | 973 | tags=10%, list=5%, signal=11% | |
150 | BIOCARTA_ION CHANNELS AND THEIR FUNCTIONAL ROLE IN VASCULAR ENDOTHELIUM | 41 | 0.54 | 1.10 | 0.318 | 0.930 | 1.000 | 1111 | tags=7%, list=6%, signal=8% | |
151 | REACTOME_RESOLUTION_OF_ABASIC_SITES__AP_SITES_ | 14 | 0.65 | 1.09 | 0.356 | 0.927 | 1.000 | 2006 | tags=43%, list=11%, signal=48% | |
152 | REACTOME_G1_S_DNA_DAMAGE_CHECKPOINTS | 40 | 0.54 | 1.09 | 0.312 | 0.922 | 1.000 | 1881 | tags=45%, list=10%, signal=50% | |
153 | REACTOME_ACTIVATION_OF_BH3_ONLY_PROTEINS | 11 | 0.67 | 1.09 | 0.378 | 0.924 | 1.000 | 1330 | tags=27%, list=7%, signal=29% | |
154 | REACTOME_SLC_MEDIATED_TRANSMEMBRANE_TRANSPORT | 57 | 0.51 | 1.09 | 0.313 | 0.928 | 1.000 | 2336 | tags=18%, list=13%, signal=20% | |
155 | BIOCARTA_CARM1 AND REGULATION OF THE ESTROGEN RECEPTOR | 11 | 0.68 | 1.09 | 0.409 | 0.924 | 1.000 | 860 | tags=18%, list=5%, signal=19% | |
156 | INOH_HETEROTRIMERIC GPCR SIGNALING PATHWAY (THROUGH G ALPHA S ACS EPAC BRAF AND ERKCASCADE) | 197 | 0.43 | 1.09 | 0.240 | 0.918 | 1.000 | 2054 | tags=8%, list=11%, signal=8% | |
157 | INOH_WNT SECRETORY PATHWAY (CANONICAL) | 47 | 0.52 | 1.08 | 0.321 | 0.930 | 1.000 | 973 | tags=11%, list=5%, signal=11% | |
158 | REACTOME_UBIQUITIN_DEPENDENT_DEGRADATION_OF_CYCLIN_D | 36 | 0.53 | 1.08 | 0.328 | 0.935 | 1.000 | 1881 | tags=50%, list=10%, signal=56% | |
159 | HUMANCYC_ISOLEUCINE DEGRADATION III | 13 | 0.66 | 1.08 | 0.394 | 0.932 | 1.000 | 1345 | tags=31%, list=7%, signal=33% | |
160 | REACTOME_METABOLISM_OF_NON_CODING_RNA | 27 | 0.57 | 1.08 | 0.348 | 0.930 | 1.000 | 2914 | tags=48%, list=16%, signal=57% | |
161 | REACTOME_P53_DEPENDENT_G1_S_DNA_DAMAGE_CHECKPOINT | 39 | 0.54 | 1.08 | 0.341 | 0.929 | 1.000 | 1881 | tags=46%, list=10%, signal=51% | |
162 | REACTOME_VIF_MEDIATED_DEGRADATION_OF_APOBEC3G | 37 | 0.54 | 1.08 | 0.353 | 0.926 | 1.000 | 1881 | tags=46%, list=10%, signal=51% | |
163 | REACTOME_TRANSPORT_OF_MATURE_MRNAS_DERIVED_FROM_INTRONLESS_TRANSCRIPTS | 20 | 0.60 | 1.07 | 0.379 | 0.928 | 1.000 | 2914 | tags=40%, list=16%, signal=47% | |
164 | REACTOME_UBIQUITIN_DEPENDENT_DEGRADATION_OF_CYCLIN_D1 | 36 | 0.53 | 1.07 | 0.352 | 0.934 | 1.000 | 1881 | tags=50%, list=10%, signal=56% | |
165 | REACTOME_AXON_GUIDANCE | 56 | 0.50 | 1.07 | 0.352 | 0.933 | 1.000 | 2213 | tags=23%, list=12%, signal=26% | |
166 | REACTOME_SPHINGOLIPID_METABOLISM | 10 | 0.66 | 1.07 | 0.416 | 0.939 | 1.000 | 2932 | tags=30%, list=16%, signal=36% | |
167 | REACTOME_RESOLUTION_OF_AP_SITES_VIA_THE_MULTIPLE_NUCLEOTIDE_PATCH_REPLACEMENT_PATHWAY | 12 | 0.65 | 1.07 | 0.418 | 0.933 | 1.000 | 1843 | tags=42%, list=10%, signal=46% | |
168 | NCI_NONCANONICAL WNT SIGNALING PATHWAY | 18 | 0.61 | 1.06 | 0.407 | 0.943 | 1.000 | 1574 | tags=17%, list=8%, signal=18% | |
169 | REACTOME_TRANSPORT_OF_MATURE_MRNA_DERIVED_FROM_AN_INTRONLESS_TRANSCRIPT | 19 | 0.60 | 1.06 | 0.403 | 0.942 | 1.000 | 2914 | tags=42%, list=16%, signal=50% | |
170 | NCI_ALPHA-SYNUCLEIN SIGNALING | 32 | 0.54 | 1.06 | 0.364 | 0.940 | 1.000 | 1682 | tags=19%, list=9%, signal=21% | |
171 | REACTOME_SCF_SKP2__MEDIATED_DEGRADATION_OF_P27_P21 | 37 | 0.53 | 1.06 | 0.367 | 0.940 | 1.000 | 2184 | tags=51%, list=12%, signal=58% | |
172 | INOH_ADENYLATE CYCLASE ACTIVATION SIGNALING | 11 | 0.64 | 1.06 | 0.404 | 0.938 | 1.000 | 564 | tags=9%, list=3%, signal=9% | |
173 | REACTOME_SEMAPHORIN_INTERACTIONS | 30 | 0.54 | 1.05 | 0.381 | 0.945 | 1.000 | 1220 | tags=20%, list=7%, signal=21% | |
174 | REACTOME_ASSEMBLY_OF_THE_PRE_REPLICATIVE_COMPLEX | 46 | 0.51 | 1.05 | 0.371 | 0.954 | 1.000 | 2225 | tags=43%, list=12%, signal=49% | |
175 | REACTOME_M_G1_TRANSITION | 46 | 0.51 | 1.04 | 0.402 | 0.973 | 1.000 | 2225 | tags=43%, list=12%, signal=49% | |
176 | REACTOME_STABILIZATION_OF_P53 | 37 | 0.52 | 1.04 | 0.398 | 0.974 | 1.000 | 1881 | tags=46%, list=10%, signal=51% | |
177 | NCI_PRESENILIN ACTION IN NOTCH AND WNT SIGNALING | 40 | 0.51 | 1.04 | 0.388 | 0.974 | 1.000 | 1030 | tags=13%, list=6%, signal=13% | |
178 | REACTOME_CYTOCHROME_P450___ARRANGED_BY_SUBSTRATE_TYPE | 19 | 0.58 | 1.04 | 0.430 | 0.969 | 1.000 | 2082 | tags=11%, list=11%, signal=12% | |
179 | BIOCARTA_EXTRINSIC PROTHROMBIN ACTIVATION PATHWAY | 12 | 0.64 | 1.04 | 0.470 | 0.974 | 1.000 | 972 | tags=17%, list=5%, signal=18% | |
180 | INOH_NOTCH SECRETORY PATHWAY (MAMMAL) | 22 | 0.56 | 1.03 | 0.433 | 0.975 | 1.000 | 1288 | tags=32%, list=7%, signal=34% | |
181 | REACTOME_REMOVAL_OF_DNA_PATCH_CONTAINING_ABASIC_RESIDUE | 11 | 0.63 | 1.03 | 0.454 | 0.971 | 1.000 | 1843 | tags=36%, list=10%, signal=40% | |
182 | REACTOME_AMINO_ACID_AND_OLIGOPEPTIDE_SLC_TRANSPORTERS | 18 | 0.59 | 1.03 | 0.448 | 0.970 | 1.000 | 403 | tags=11%, list=2%, signal=11% | |
183 | INOH_MAMMALIAN NOTCH SIGNALING PATHWAY | 22 | 0.56 | 1.03 | 0.423 | 0.966 | 1.000 | 1288 | tags=32%, list=7%, signal=34% | |
184 | REACTOME_S_PHASE | 74 | 0.47 | 1.03 | 0.408 | 0.963 | 1.000 | 2800 | tags=49%, list=15%, signal=57% | |
185 | REACTOME_AUTODEGRADATION_OF_THE_E3_UBIQUITIN_LIGASE_COP1 | 36 | 0.52 | 1.03 | 0.398 | 0.964 | 1.000 | 1881 | tags=47%, list=10%, signal=52% | |
186 | NCI_FOXM1 TRANSCRIPTION FACTOR NETWORK | 34 | 0.52 | 1.03 | 0.428 | 0.963 | 1.000 | 2631 | tags=32%, list=14%, signal=38% | |
187 | REACTOME_FORMATION_OF_HIV_1_ELONGATION_COMPLEX_CONTAINING_HIV_1_TAT | 28 | 0.54 | 1.03 | 0.418 | 0.960 | 1.000 | 3436 | tags=61%, list=18%, signal=74% | |
188 | REACTOME_SCF_BETA_TRCP_MEDIATED_DEGRADATION_OF_EMI1 | 35 | 0.51 | 1.03 | 0.406 | 0.957 | 1.000 | 2184 | tags=51%, list=12%, signal=58% | |
189 | BIOCARTA_HYPOXIA-INDUCIBLE FACTOR IN THE CARDIVASCULAR SYSTEM | 14 | 0.60 | 1.03 | 0.459 | 0.952 | 1.000 | 1291 | tags=21%, list=7%, signal=23% | |
190 | INOH_HETEROTRIMERIC GPCR SIGNALING PATHWAY (THROUGH G ALPHA Q, PLC BETA AND ERK CASCADE) | 185 | 0.41 | 1.03 | 0.401 | 0.953 | 1.000 | 2264 | tags=9%, list=12%, signal=10% | |
191 | REACTOME_TAT_MEDIATED_ELONGATION_OF_THE_HIV_1_TRANSCRIPT | 28 | 0.54 | 1.02 | 0.425 | 0.952 | 1.000 | 3436 | tags=61%, list=18%, signal=74% | |
192 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION_ELONGATION | 29 | 0.54 | 1.02 | 0.450 | 0.949 | 1.000 | 3436 | tags=59%, list=18%, signal=72% | |
193 | BIOCARTA_ER ASSOCIATED DEGRADATION (ERAD) PATHWAY | 15 | 0.60 | 1.02 | 0.470 | 0.944 | 1.000 | 2338 | tags=40%, list=13%, signal=46% | |
194 | REACTOME_CDC20_PHOSPHO_APC_C_MEDIATED_DEGRADATION_OF_CYCLIN_A | 42 | 0.50 | 1.02 | 0.441 | 0.943 | 1.000 | 2184 | tags=45%, list=12%, signal=51% | |
195 | REACTOME_FORMATION_OF_RNA_POL_II_ELONGATION_COMPLEX_ | 29 | 0.54 | 1.02 | 0.440 | 0.940 | 1.000 | 3436 | tags=59%, list=18%, signal=72% | |
196 | HUMANCYC_NAD/NADH PHOSPHORYLATION AND DEPHOSPHORYLATION | 30 | 0.53 | 1.02 | 0.447 | 0.937 | 1.000 | 2652 | tags=57%, list=14%, signal=66% | |
197 | NCI_EPHRIN B REVERSE SIGNALING | 27 | 0.55 | 1.02 | 0.446 | 0.933 | 1.000 | 1040 | tags=19%, list=6%, signal=20% | |
198 | BIOCARTA_FL-ARRESTINS IN GPCR DESENSITIZATION | 26 | 0.54 | 1.02 | 0.434 | 0.932 | 1.000 | 1861 | tags=15%, list=10%, signal=17% | |
199 | REACTOME_PURINE_SALVAGE_REACTIONS | 10 | 0.66 | 1.02 | 0.506 | 0.928 | 1.000 | 1321 | tags=30%, list=7%, signal=32% | |
200 | REACTOME_TRANSMISSION_ACROSS_CHEMICAL_SYNAPSES | 41 | 0.50 | 1.02 | 0.415 | 0.934 | 1.000 | 1567 | tags=20%, list=8%, signal=21% | |
201 | REACTOME_REGULATION_OF_ORNITHINE_DECARBOXYLASE__ODC_ | 38 | 0.50 | 1.01 | 0.424 | 0.934 | 1.000 | 1881 | tags=42%, list=10%, signal=47% | |
202 | REACTOME_REGULATORY_RNA_PATHWAYS | 10 | 0.62 | 1.01 | 0.497 | 0.930 | 1.000 | 3413 | tags=60%, list=18%, signal=73% | |
203 | REACTOME_HIV_1_TRANSCRIPTION_ELONGATION | 28 | 0.54 | 1.01 | 0.449 | 0.926 | 1.000 | 3436 | tags=61%, list=18%, signal=74% | |
204 | REACTOME_APC_C_MEDIATED_DEGRADATION_OF_CELL_CYCLE_PROTEINS | 47 | 0.49 | 1.01 | 0.429 | 0.922 | 1.000 | 2184 | tags=45%, list=12%, signal=50% | |
205 | REACTOME_TRANSPORT_OF_THE_SLBP_INDEPENDENT_MATURE_MRNA | 18 | 0.56 | 1.01 | 0.440 | 0.920 | 1.000 | 2914 | tags=39%, list=16%, signal=46% | |
206 | REACTOME_PLATELET_AGGREGATION__PLUG_FORMATION_ | 18 | 0.57 | 1.01 | 0.460 | 0.919 | 1.000 | 2213 | tags=11%, list=12%, signal=13% | |
207 | REACTOME_APC_C_CDH1_MEDIATED_DEGRADATION_OF_CDC20_AND_OTHER_APC_C_CDH1_TARGETED_PROTEINS_IN_LATE_MITOSIS_EARLY_G1 | 39 | 0.50 | 1.01 | 0.442 | 0.922 | 1.000 | 2184 | tags=46%, list=12%, signal=52% | |
208 | REACTOME_APC_C_CDC20_MEDIATED_DEGRADATION_OF_MITOTIC_PROTEINS | 44 | 0.49 | 1.01 | 0.447 | 0.919 | 1.000 | 2184 | tags=45%, list=12%, signal=51% | |
209 | REACTOME_TRANSPORT_OF_THE_SLBP_DEPENDANT_MATURE_MRNA | 19 | 0.56 | 1.01 | 0.448 | 0.919 | 1.000 | 2914 | tags=37%, list=16%, signal=44% | |
210 | REACTOME_TRANSMEMBRANE_TRANSPORT_OF_SMALL_MOLECULES | 64 | 0.46 | 1.01 | 0.431 | 0.916 | 1.000 | 2336 | tags=19%, list=13%, signal=21% | |
211 | HUMANCYC_SALVAGE PATHWAYS OF PYRIMIDINE RIBONUCLEOTIDES | 12 | 0.62 | 1.01 | 0.497 | 0.913 | 1.000 | 2175 | tags=42%, list=12%, signal=47% | |
212 | REACTOME_CYCLIN_E_ASSOCIATED_EVENTS_DURING_G1_S_TRANSITION_ | 44 | 0.48 | 1.00 | 0.441 | 0.918 | 1.000 | 2311 | tags=45%, list=12%, signal=52% | |
213 | REACTOME_P53_INDEPENDENT_DNA_DAMAGE_RESPONSE | 35 | 0.50 | 1.00 | 0.452 | 0.918 | 1.000 | 1881 | tags=46%, list=10%, signal=51% | |
214 | REACTOME_CDT1_ASSOCIATION_WITH_THE_CDC6_ORC_ORIGIN_COMPLEX | 39 | 0.50 | 1.00 | 0.455 | 0.920 | 1.000 | 1881 | tags=41%, list=10%, signal=46% | |
215 | INOH_HETEROMERIC GPCR SIGNALING PATHWAY (THROUGH_G ALPHA S_ACS_PKA_BRAF_AND_ERKCASCADE)(CANONICAL) | 189 | 0.40 | 1.00 | 0.446 | 0.919 | 1.000 | 2054 | tags=7%, list=11%, signal=8% | |
216 | REACTOME_REGULATION_OF_APOPTOSIS | 36 | 0.49 | 1.00 | 0.466 | 0.914 | 1.000 | 1881 | tags=44%, list=10%, signal=49% | |
217 | REACTOME_INTEGRIN_ALPHAIIBBETA3_SIGNALING | 17 | 0.57 | 1.00 | 0.475 | 0.912 | 1.000 | 2213 | tags=12%, list=12%, signal=13% | |
218 | REACTOME_ACTIVATION_OF_APC_C_AND_APC_C_CDC20_MEDIATED_DEGRADATION_OF_MITOTIC_PROTEINS | 45 | 0.49 | 1.00 | 0.459 | 0.911 | 1.000 | 2184 | tags=44%, list=12%, signal=50% | |
219 | BIOCARTA_IL 6 SIGNALING PATHWAY | 13 | 0.61 | 1.00 | 0.506 | 0.909 | 1.000 | 2319 | tags=31%, list=12%, signal=35% | |
220 | REACTOME_REGULATION_OF_APC_C_ACTIVATORS_BETWEEN_G1_S_AND_EARLY_ANAPHASE | 46 | 0.48 | 1.00 | 0.443 | 0.905 | 1.000 | 2184 | tags=43%, list=12%, signal=49% | |
221 | REACTOME_CELL_CYCLE_CHECKPOINTS | 75 | 0.45 | 1.00 | 0.476 | 0.901 | 1.000 | 2770 | tags=43%, list=15%, signal=50% | |
222 | REACTOME_ORNITHINE_AND_PROLINE_METABOLISM | 46 | 0.48 | 1.00 | 0.485 | 0.897 | 1.000 | 1881 | tags=41%, list=10%, signal=46% | |
223 | BIOCARTA_MULTIPLE ANTIAPOPTOTIC PATHWAYS FROM IGF-1R SIGNALING LEAD TO BAD PHOSPHORYLATION | 13 | 0.60 | 1.00 | 0.505 | 0.894 | 1.000 | 2319 | tags=31%, list=12%, signal=35% | |
224 | NCI_THROMBOXANE A2 RECEPTOR SIGNALING | 50 | 0.48 | 1.00 | 0.469 | 0.892 | 1.000 | 1871 | tags=16%, list=10%, signal=18% | |
225 | REACTOME_AUTODEGRADATION_OF_CDH1_BY_CDH1_APC_C | 38 | 0.50 | 1.00 | 0.470 | 0.889 | 1.000 | 1881 | tags=42%, list=10%, signal=47% | |
226 | REACTOME_REMOVAL_OF_LICENSING_FACTORS_FROM_ORIGINS | 48 | 0.48 | 1.00 | 0.468 | 0.886 | 1.000 | 2225 | tags=42%, list=12%, signal=47% | |
227 | REACTOME_UBIQUITIN_MEDIATED_DEGRADATION_OF_PHOSPHORYLATED_CDC25A | 35 | 0.50 | 0.99 | 0.462 | 0.884 | 1.000 | 1881 | tags=46%, list=10%, signal=51% | |
228 | REACTOME_ORC1_REMOVAL_FROM_CHROMATIN | 46 | 0.48 | 0.99 | 0.471 | 0.883 | 1.000 | 2225 | tags=43%, list=12%, signal=49% | |
229 | REACTOME_REGULATION_OF_DNA_REPLICATION | 49 | 0.48 | 0.99 | 0.460 | 0.879 | 1.000 | 2225 | tags=41%, list=12%, signal=46% | |
230 | REACTOME_ELONGATION_ARREST_AND_RECOVERY | 20 | 0.54 | 0.99 | 0.463 | 0.879 | 1.000 | 3436 | tags=60%, list=18%, signal=74% | |
231 | REACTOME_SWITCHING_OF_ORIGINS_TO_A_POST_REPLICATIVE_STATE | 46 | 0.48 | 0.99 | 0.490 | 0.876 | 1.000 | 2225 | tags=43%, list=12%, signal=49% | |
232 | BIOCARTA_ROLE OF BRCA1 BRCA2 AND ATR IN CANCER SUSCEPTIBILITY | 21 | 0.54 | 0.99 | 0.491 | 0.877 | 1.000 | 2636 | tags=19%, list=14%, signal=22% | |
233 | BIOCARTA_IL12 AND STAT4 DEPENDENT SIGNALING PATHWAY IN TH1 DEVELOPMENT | 15 | 0.58 | 0.99 | 0.502 | 0.874 | 1.000 | 1953 | tags=27%, list=10%, signal=30% | |
234 | REACTOME_RNA_POLYMERASE_II_PROMOTER_ESCAPE | 32 | 0.50 | 0.99 | 0.474 | 0.872 | 1.000 | 3436 | tags=41%, list=18%, signal=50% | |
235 | REACTOME_CDK_MEDIATED_PHOSPHORYLATION_AND_REMOVAL_OF_CDC6 | 35 | 0.49 | 0.99 | 0.490 | 0.871 | 1.000 | 1881 | tags=46%, list=10%, signal=51% | |
236 | BIOCARTA_CDK REGULATION OF DNA REPLICATION | 18 | 0.56 | 0.99 | 0.460 | 0.870 | 1.000 | 2686 | tags=39%, list=14%, signal=45% | |
237 | REACTOME_METABOLISM_OF_LIPIDS_AND_LIPOPROTEINS | 110 | 0.42 | 0.99 | 0.479 | 0.869 | 1.000 | 2654 | tags=20%, list=14%, signal=23% | |
238 | BIOCARTA_ASPIRIN BLOCKS SIGNALING PATHWAY INVOLVED IN PLATELET ACTIVATION | 16 | 0.57 | 0.99 | 0.491 | 0.867 | 1.000 | 2082 | tags=31%, list=11%, signal=35% | |
239 | REACTOME_CYCLIN_A_CDK2_ASSOCIATED_EVENTS_AT_S_PHASE_ENTRY | 43 | 0.49 | 0.99 | 0.481 | 0.864 | 1.000 | 2311 | tags=47%, list=12%, signal=53% | |
240 | REACTOME_REGULATION_OF_ACTIVATED_PAK_2P34_BY_PROTEASOME_MEDIATED_DEGRADATION1 | 34 | 0.50 | 0.98 | 0.498 | 0.866 | 1.000 | 1881 | tags=47%, list=10%, signal=52% | |
241 | REACTOME_P53_INDEPENDENT_G1_S_DNA_DAMAGE_CHECKPOINT | 35 | 0.50 | 0.98 | 0.494 | 0.864 | 1.000 | 1881 | tags=46%, list=10%, signal=51% | |
242 | REACTOME_HIV_1_ELONGATION_ARREST_AND_RECOVERY | 20 | 0.54 | 0.98 | 0.497 | 0.867 | 1.000 | 3436 | tags=60%, list=18%, signal=74% | |
243 | REACTOME_RNA_POLYMERASE_II_HIV_1_PROMOTER_ESCAPE | 32 | 0.50 | 0.98 | 0.496 | 0.865 | 1.000 | 3436 | tags=41%, list=18%, signal=50% | |
244 | REACTOME_SIGNALING_BY_WNT | 37 | 0.49 | 0.98 | 0.493 | 0.862 | 1.000 | 2184 | tags=49%, list=12%, signal=55% | |
245 | INOH_DROSOPHILA WINGLESS/WNT SIGNALING PATHWAY | 13 | 0.59 | 0.98 | 0.522 | 0.859 | 1.000 | 1388 | tags=38%, list=7%, signal=42% | |
246 | REACTOME_HIV_1_TRANSCRIPTION_INITIATION | 32 | 0.50 | 0.98 | 0.498 | 0.856 | 1.000 | 3436 | tags=41%, list=18%, signal=50% | |
247 | BIOCARTA_STRESS INDUCTION OF HSP REGULATION | 14 | 0.58 | 0.98 | 0.526 | 0.853 | 1.000 | 823 | tags=14%, list=4%, signal=15% | |
248 | REACTOME_SYNAPTIC_TRANSMISSION | 42 | 0.49 | 0.98 | 0.487 | 0.850 | 1.000 | 1567 | tags=19%, list=8%, signal=21% | |
249 | REACTOME_PAUSING_AND_RECOVERY_OF_ELONGATION | 20 | 0.54 | 0.98 | 0.495 | 0.848 | 1.000 | 3436 | tags=60%, list=18%, signal=74% | |
250 | REACTOME_PAUSING_AND_RECOVERY_OF_HIV_1_ELONGATION | 20 | 0.54 | 0.98 | 0.502 | 0.848 | 1.000 | 3436 | tags=60%, list=18%, signal=74% | |
251 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION_PRE_INITIATION | 32 | 0.50 | 0.97 | 0.514 | 0.850 | 1.000 | 3436 | tags=41%, list=18%, signal=50% | |
252 | REACTOME_REGULATION_OF_ACTIVATED_PAK_2P34_BY_PROTEASOME_MEDIATED_DEGRADATION | 35 | 0.49 | 0.97 | 0.509 | 0.849 | 1.000 | 1881 | tags=46%, list=10%, signal=51% | |
253 | REACTOME_TRANSCRIPTION_COUPLED_NER__TC_NER_ | 33 | 0.49 | 0.97 | 0.512 | 0.853 | 1.000 | 2311 | tags=42%, list=12%, signal=48% | |
254 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION_INITIATION | 32 | 0.50 | 0.97 | 0.503 | 0.850 | 1.000 | 3436 | tags=41%, list=18%, signal=50% | |
255 | BIOCARTA_ROLE OF MITOCHONDRIA IN APOPTOTIC SIGNALING | 12 | 0.59 | 0.97 | 0.537 | 0.853 | 1.000 | 208 | tags=17%, list=1%, signal=17% | |
256 | REACTOME_HORMONE_BIOSYNTHESIS | 31 | 0.50 | 0.97 | 0.509 | 0.852 | 1.000 | 2139 | tags=16%, list=11%, signal=18% | |
257 | REACTOME_GLUCOSE_UPTAKE | 22 | 0.53 | 0.97 | 0.505 | 0.850 | 1.000 | 2914 | tags=32%, list=16%, signal=38% | |
258 | REACTOME_TAT_MEDIATED_HIV_1_ELONGATION_ARREST_AND_RECOVERY_ | 19 | 0.54 | 0.97 | 0.505 | 0.849 | 1.000 | 3436 | tags=63%, list=18%, signal=77% | |
259 | BIOCARTA_APOPTOTIC SIGNALING IN RESPONSE TO DNA DAMAGE | 14 | 0.57 | 0.96 | 0.553 | 0.849 | 1.000 | 1101 | tags=29%, list=6%, signal=30% | |
260 | REACTOME_PAUSING_AND_RECOVERY_OF_TAT_MEDIATED_HIV_1_ELONGATION | 19 | 0.54 | 0.96 | 0.540 | 0.856 | 1.000 | 3436 | tags=63%, list=18%, signal=77% | |
261 | BIOCARTA_IL 2 SIGNALING PATHWAY | 14 | 0.58 | 0.96 | 0.553 | 0.853 | 1.000 | 2319 | tags=36%, list=12%, signal=41% | |
262 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION_INITIATION_AND_PROMOTER_CLEARANCE | 32 | 0.50 | 0.96 | 0.542 | 0.853 | 1.000 | 3436 | tags=41%, list=18%, signal=50% | |
263 | REACTOME_HIV_1_TRANSCRIPTION_PRE_INITIATION | 32 | 0.50 | 0.96 | 0.504 | 0.852 | 1.000 | 3436 | tags=41%, list=18%, signal=50% | |
264 | NCI_FOXA1 TRANSCRIPTION FACTOR NETWORK | 33 | 0.48 | 0.96 | 0.496 | 0.857 | 1.000 | 1333 | tags=12%, list=7%, signal=13% | |
265 | REACTOME_NUCLEOTIDE_EXCISION_REPAIR | 37 | 0.48 | 0.95 | 0.545 | 0.855 | 1.000 | 3413 | tags=54%, list=18%, signal=66% | |
266 | REACTOME_RNA_POLYMERASE_III_TRANSCRIPTION_INITIATION_FROM_TYPE_3_PROMOTER | 10 | 0.61 | 0.95 | 0.579 | 0.854 | 1.000 | 3345 | tags=60%, list=18%, signal=73% | |
267 | REACTOME_SYNTHESIS_OF_DNA | 65 | 0.43 | 0.95 | 0.510 | 0.859 | 1.000 | 2800 | tags=48%, list=15%, signal=56% | |
268 | BIOCARTA_ROLE OF FL-ARRESTINS IN THE ACTIVATION AND TARGETING OF MAP KINASES | 28 | 0.50 | 0.95 | 0.534 | 0.857 | 1.000 | 1667 | tags=14%, list=9%, signal=16% | |
269 | NCI_SIGNALING EVENTS MEDIATED BY HDAC CLASS I | 90 | 0.42 | 0.95 | 0.557 | 0.856 | 1.000 | 2010 | tags=26%, list=11%, signal=29% | |
270 | INOH_TGF BETA SIGNALING PATHWAY(THROUGH TAK1) | 13 | 0.57 | 0.94 | 0.569 | 0.872 | 1.000 | 2790 | tags=23%, list=15%, signal=27% | |
271 | NCI_PROTEOGYLCAN SYNDECAN-MEDIATED SIGNALING EVENTS | 229 | 0.38 | 0.94 | 0.632 | 0.877 | 1.000 | 1861 | tags=14%, list=10%, signal=16% | |
272 | NCI_SIGNALING EVENTS MEDIATED BY PTP1B | 46 | 0.45 | 0.94 | 0.572 | 0.875 | 1.000 | 2319 | tags=17%, list=12%, signal=20% | |
273 | REACTOME_TRANSCRIPTION | 92 | 0.41 | 0.93 | 0.587 | 0.882 | 1.000 | 1998 | tags=22%, list=11%, signal=24% | |
274 | BIOCARTA_MELANOCYTE DEVELOPMENT AND PIGMENTATION PATHWAY | 12 | 0.56 | 0.93 | 0.547 | 0.881 | 1.000 | 1667 | tags=25%, list=9%, signal=27% | |
275 | INOH_CANONICAL NOTCH SIGNALING PATHWAY | 26 | 0.50 | 0.93 | 0.549 | 0.880 | 1.000 | 1288 | tags=23%, list=7%, signal=25% | |
276 | NCI_FAS SIGNALING PATHWAY (CD95) | 31 | 0.48 | 0.93 | 0.587 | 0.886 | 1.000 | 208 | tags=10%, list=1%, signal=10% | |
277 | REACTOME_RNA_POLYMERASE_I_CHAIN_ELONGATION | 15 | 0.55 | 0.93 | 0.614 | 0.884 | 1.000 | 2311 | tags=40%, list=12%, signal=46% | |
278 | BIOCARTA_CORTICOSTEROIDS AND CARDIOPROTECTION | 25 | 0.49 | 0.93 | 0.582 | 0.882 | 1.000 | 1111 | tags=12%, list=6%, signal=13% | |
279 | NCI_FOXA TRANSCRIPTION FACTOR NETWORKS | 65 | 0.42 | 0.93 | 0.574 | 0.881 | 1.000 | 1333 | tags=11%, list=7%, signal=12% | |
280 | BIOCARTA_REGULATION OF P27 PHOSPHORYLATION DURING CELL CYCLE PROGRESSION | 11 | 0.58 | 0.92 | 0.603 | 0.885 | 1.000 | 2631 | tags=55%, list=14%, signal=63% | |
281 | HUMANCYC_SUPERPATHWAY OF CITRULLINE METABOLISM | 11 | 0.57 | 0.92 | 0.608 | 0.882 | 1.000 | 1298 | tags=27%, list=7%, signal=29% | |
282 | INOH_NOTCH SECRETORY PATHWAY | 26 | 0.50 | 0.92 | 0.564 | 0.880 | 1.000 | 1288 | tags=23%, list=7%, signal=25% | |
283 | REACTOME_TRANSPORT_OF_MATURE_TRANSCRIPT_TO_CYTOPLASM | 33 | 0.47 | 0.92 | 0.586 | 0.882 | 1.000 | 2317 | tags=27%, list=12%, signal=31% | |
284 | NCI_FOXA2 AND FOXA3 TRANSCRIPTION FACTOR NETWORKS | 37 | 0.46 | 0.92 | 0.610 | 0.884 | 1.000 | 1214 | tags=11%, list=7%, signal=12% | |
285 | REACTOME_VPU_MEDIATED_DEGRADATION_OF_CD4 | 35 | 0.47 | 0.92 | 0.606 | 0.883 | 1.000 | 1881 | tags=46%, list=10%, signal=51% | |
286 | REACTOME_AMINE_COMPOUND_SLC_TRANSPORTERS | 10 | 0.58 | 0.92 | 0.606 | 0.882 | 1.000 | 292 | tags=10%, list=2%, signal=10% | |
287 | BIOCARTA_REGULATION OF EIF2 | 10 | 0.59 | 0.91 | 0.628 | 0.885 | 1.000 | 522 | tags=20%, list=3%, signal=21% | |
288 | REACTOME_SYNTHESIS_OF_BILE_ACIDS_AND_BILE_SALTS | 10 | 0.58 | 0.91 | 0.611 | 0.886 | 1.000 | 4024 | tags=20%, list=22%, signal=26% | |
289 | BIOCARTA_ALK IN CARDIAC MYOCYTES | 27 | 0.48 | 0.91 | 0.613 | 0.892 | 1.000 | 275 | tags=7%, list=1%, signal=8% | |
290 | REACTOME_PLATELET_ACTIVATION | 69 | 0.41 | 0.91 | 0.640 | 0.891 | 1.000 | 1695 | tags=14%, list=9%, signal=16% | |
291 | BIOCARTA_AGRIN IN POSTSYNAPTIC DIFFERENTIATION | 44 | 0.44 | 0.91 | 0.622 | 0.892 | 1.000 | 2500 | tags=18%, list=13%, signal=21% | |
292 | HUMANCYC_DE NOVO BIOSYNTHESIS OF PYRIMIDINE DEOXYRIBONUCLEOTIDES | 11 | 0.56 | 0.91 | 0.632 | 0.889 | 1.000 | 2352 | tags=45%, list=13%, signal=52% | |
293 | REACTOME_DNA_REPAIR | 66 | 0.41 | 0.90 | 0.629 | 0.888 | 1.000 | 2636 | tags=30%, list=14%, signal=35% | |
294 | NETPATH_NGF | 45 | 0.44 | 0.90 | 0.623 | 0.895 | 1.000 | 2319 | tags=24%, list=12%, signal=28% | |
295 | REACTOME_TRANSCRIPTION_OF_THE_HIV_GENOME | 44 | 0.43 | 0.90 | 0.614 | 0.904 | 1.000 | 3436 | tags=41%, list=18%, signal=50% | |
296 | REACTOME_METABOLISM_OF_BILE_ACIDS_AND_BILE_SALTS | 14 | 0.53 | 0.89 | 0.640 | 0.902 | 1.000 | 4896 | tags=21%, list=26%, signal=29% | |
297 | REACTOME_TOLL_LIKE_RECEPTOR_3__TLR3__CASCADE | 14 | 0.53 | 0.89 | 0.611 | 0.902 | 1.000 | 1928 | tags=21%, list=10%, signal=24% | |
298 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION | 67 | 0.40 | 0.89 | 0.671 | 0.904 | 1.000 | 2457 | tags=24%, list=13%, signal=27% | |
299 | NCI_SYNDECAN-3-MEDIATED SIGNALING EVENTS | 13 | 0.54 | 0.89 | 0.642 | 0.905 | 1.000 | 1255 | tags=23%, list=7%, signal=25% | |
300 | REACTOME_TRANSPORT_OF_MATURE_MRNA_DERIVED_FROM_AN_INTRON_CONTAINING_TRANSCRIPT | 31 | 0.46 | 0.89 | 0.654 | 0.908 | 1.000 | 2317 | tags=26%, list=12%, signal=29% | |
301 | REACTOME_TRAF6_MEDIATED_INDUCTION_OF_THE_ANTIVIRAL_CYTOKINE_IFN_ALPHA_BETA_CASCADE | 12 | 0.54 | 0.88 | 0.645 | 0.909 | 1.000 | 1928 | tags=25%, list=10%, signal=28% | |
302 | INOH_TGF BETA RECEPTOR COMPLEX DEGRADATION SIGNALING | 29 | 0.46 | 0.88 | 0.631 | 0.907 | 1.000 | 1881 | tags=41%, list=10%, signal=46% | |
303 | REACTOME_G1_S_TRANSITION | 75 | 0.39 | 0.88 | 0.675 | 0.910 | 1.000 | 2770 | tags=40%, list=15%, signal=47% | |
304 | REACTOME_DNA_REPLICATION | 69 | 0.40 | 0.88 | 0.709 | 0.912 | 1.000 | 2800 | tags=45%, list=15%, signal=53% | |
305 | INOH_XENOPUS AXIS FORMATION WNT SIGNALING PATHWAY | 42 | 0.42 | 0.88 | 0.651 | 0.909 | 1.000 | 612 | tags=5%, list=3%, signal=5% | |
306 | BIOCARTA_ROLE OF NICOTINIC ACETYLCHOLINE RECEPTORS IN THE REGULATION OF APOPTOSIS | 17 | 0.50 | 0.88 | 0.644 | 0.912 | 1.000 | 1101 | tags=18%, list=6%, signal=19% | |
307 | REACTOME_INTRINSIC_PATHWAY_FOR_APOPTOSIS | 22 | 0.47 | 0.88 | 0.625 | 0.912 | 1.000 | 1330 | tags=18%, list=7%, signal=20% | |
308 | INOH_TOLL-LIKE RECEPTOR SIGNALING PATHWAY (THROUGH LPS, TLR4, MYD88, IRAK, TAK1 AND IKK-NF-KAPPAB CASCADE)(CANONICAL) | 22 | 0.48 | 0.87 | 0.652 | 0.916 | 1.000 | 3117 | tags=41%, list=17%, signal=49% | |
309 | BIOCARTA_P53 SIGNALING PATHWAY | 13 | 0.52 | 0.87 | 0.673 | 0.916 | 1.000 | 1330 | tags=38%, list=7%, signal=41% | |
310 | REACTOME_SIGNALING_IN_IMMUNE_SYSTEM | 136 | 0.37 | 0.87 | 0.783 | 0.916 | 1.000 | 896 | tags=9%, list=5%, signal=9% | |
311 | REACTOME_NEP_NS2_INTERACTS_WITH_THE_CELLULAR_EXPORT_MACHINERY | 17 | 0.49 | 0.87 | 0.652 | 0.915 | 1.000 | 2914 | tags=29%, list=16%, signal=35% | |
312 | REACTOME_FORMATION_OF_PLATELET_PLUG | 81 | 0.38 | 0.87 | 0.724 | 0.917 | 1.000 | 1695 | tags=12%, list=9%, signal=14% | |
313 | HUMANCYC_TRIACYLGLYCEROL DEGRADATION | 12 | 0.53 | 0.86 | 0.659 | 0.918 | 1.000 | 3536 | tags=25%, list=19%, signal=31% | |
314 | HUMANCYC_PHOSPHOLIPASES | 22 | 0.48 | 0.86 | 0.663 | 0.916 | 1.000 | 2264 | tags=9%, list=12%, signal=10% | |
315 | REACTOME_SEMA4D_IN_SEMAPHORIN_SIGNALING | 12 | 0.53 | 0.86 | 0.665 | 0.914 | 1.000 | 1220 | tags=25%, list=7%, signal=27% | |
316 | NCI_ANGIOPOIETIN RECEPTOR TIE2-MEDIATED SIGNALING | 44 | 0.42 | 0.86 | 0.705 | 0.914 | 1.000 | 2319 | tags=14%, list=12%, signal=16% | |
317 | REACTOME_HEMOSTASIS | 147 | 0.36 | 0.86 | 0.781 | 0.912 | 1.000 | 1695 | tags=12%, list=9%, signal=13% | |
318 | REACTOME_RNA_POLYMERASE_I_TRANSCRIPTION_TERMINATION | 16 | 0.50 | 0.86 | 0.662 | 0.914 | 1.000 | 2311 | tags=38%, list=12%, signal=43% | |
319 | HUMANCYC_FATTY ACID BETA-OXIDATION I | 16 | 0.50 | 0.86 | 0.700 | 0.914 | 1.000 | 1749 | tags=19%, list=9%, signal=21% | |
320 | BIOCARTA_FIBRINOLYSIS PATHWAY | 12 | 0.52 | 0.86 | 0.679 | 0.914 | 1.000 | 113 | tags=8%, list=1%, signal=8% | |
321 | BIOCARTA_REGULATION OF EIF-4E AND P70S6 KINASE | 22 | 0.47 | 0.86 | 0.687 | 0.915 | 1.000 | 39 | tags=9%, list=0%, signal=9% | |
322 | REACTOME_HIV_INFECTION | 121 | 0.36 | 0.86 | 0.808 | 0.912 | 1.000 | 2770 | tags=31%, list=15%, signal=37% | |
323 | INOH_ERK CASCADE | 12 | 0.51 | 0.85 | 0.691 | 0.913 | 1.000 | 3576 | tags=42%, list=19%, signal=52% | |
324 | INOH_MAMMALIAN WNT SIGNALING PATHWAY | 70 | 0.39 | 0.85 | 0.744 | 0.913 | 1.000 | 1388 | tags=10%, list=7%, signal=11% | |
325 | REACTOME_RNA_POLYMERASE_I_TRANSCRIPTION_INITIATION | 15 | 0.50 | 0.85 | 0.708 | 0.915 | 1.000 | 2311 | tags=40%, list=12%, signal=46% | |
326 | REACTOME_EXPORT_OF_VIRAL_RIBONUCLEOPROTEINS_FROM_NUCLEUS | 17 | 0.49 | 0.85 | 0.691 | 0.917 | 1.000 | 2914 | tags=29%, list=16%, signal=35% | |
327 | NCI_EPHRINA-EPHA PATHWAY | 40 | 0.41 | 0.85 | 0.725 | 0.915 | 1.000 | 726 | tags=8%, list=4%, signal=8% | |
328 | REACTOME_NEGATIVE_REGULATION_OF_GLUCOKINASE_BY_GLUCOKINASE_REGULATORY_PROTEIN | 16 | 0.49 | 0.85 | 0.680 | 0.914 | 1.000 | 2914 | tags=31%, list=16%, signal=37% | |
329 | INOH_IKK-NF-KAPPAB CASCADE | 12 | 0.51 | 0.85 | 0.674 | 0.914 | 1.000 | 1928 | tags=25%, list=10%, signal=28% | |
330 | INOH_INTEGRIN SIGNALING PATHWAY | 92 | 0.37 | 0.85 | 0.780 | 0.911 | 1.000 | 1693 | tags=12%, list=9%, signal=13% | |
331 | INOH_TOLL-LIKE RECEPTOR SIGNALING PATHWAY (P38 CASCADE) | 24 | 0.46 | 0.84 | 0.711 | 0.910 | 1.000 | 1290 | tags=17%, list=7%, signal=18% | |
332 | REACTOME_APOPTOSIS | 94 | 0.37 | 0.84 | 0.814 | 0.908 | 1.000 | 2213 | tags=26%, list=12%, signal=29% | |
333 | REACTOME_GOLGI_ASSOCIATED_VESICLE_BIOGENESIS | 12 | 0.51 | 0.84 | 0.677 | 0.905 | 1.000 | 2484 | tags=33%, list=13%, signal=38% | |
334 | REACTOME_POST_ELONGATION_PROCESSING_OF_INTRON_CONTAINING_PRE_MRNA | 23 | 0.45 | 0.84 | 0.698 | 0.911 | 1.000 | 1972 | tags=26%, list=11%, signal=29% | |
335 | INOH_CYTOKINE RECEPTOR DEGRADATION SIGNALING | 20 | 0.46 | 0.84 | 0.708 | 0.909 | 1.000 | 1881 | tags=60%, list=10%, signal=67% | |
336 | REACTOME_POST_ELONGATION_PROCESSING_OF_THE_TRANSCRIPT | 23 | 0.45 | 0.84 | 0.707 | 0.907 | 1.000 | 1972 | tags=26%, list=11%, signal=29% | |
337 | NCI_EPHRINB-EPHB PATHWAY | 52 | 0.39 | 0.84 | 0.749 | 0.906 | 1.000 | 2319 | tags=21%, list=12%, signal=24% | |
338 | REACTOME_MRNA_3__END_PROCESSING | 23 | 0.45 | 0.83 | 0.708 | 0.910 | 1.000 | 1972 | tags=26%, list=11%, signal=29% | |
339 | NETPATH_IFN-GAMMA | 67 | 0.38 | 0.83 | 0.786 | 0.908 | 1.000 | 2686 | tags=33%, list=14%, signal=38% | |
340 | INOH_PKA ACTIVATION SIGNALING | 46 | 0.40 | 0.83 | 0.735 | 0.911 | 1.000 | 564 | tags=4%, list=3%, signal=4% | |
341 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION_TERMINATION | 23 | 0.45 | 0.83 | 0.710 | 0.908 | 1.000 | 1972 | tags=26%, list=11%, signal=29% | |
342 | INOH_TGF BETA RECEPTOR I DEGRADATION SIGNALING | 25 | 0.44 | 0.83 | 0.710 | 0.906 | 1.000 | 1881 | tags=44%, list=10%, signal=49% | |
343 | REACTOME_CLEAVAGE_OF_GROWING_TRANSCRIPT_IN_THE_TERMINATION_REGION_ | 23 | 0.45 | 0.83 | 0.721 | 0.904 | 1.000 | 1972 | tags=26%, list=11%, signal=29% | |
344 | BIOCARTA_CONTROL OF GENE EXPRESSION BY VITAMIN D RECEPTOR | 22 | 0.45 | 0.83 | 0.734 | 0.911 | 1.000 | 1890 | tags=27%, list=10%, signal=30% | |
345 | INOH_SIGNALING WITH WNT (XENOPUS) | 16 | 0.48 | 0.83 | 0.714 | 0.909 | 1.000 | 60 | tags=6%, list=0%, signal=6% | |
346 | INOH_CANONICAL WNT SIGNALING PATHWAY | 73 | 0.37 | 0.83 | 0.805 | 0.908 | 1.000 | 1388 | tags=10%, list=7%, signal=10% | |
347 | REACTOME_CELL_CYCLE__MITOTIC | 143 | 0.34 | 0.82 | 0.879 | 0.908 | 1.000 | 2800 | tags=30%, list=15%, signal=35% | |
348 | INOH_STABILIZATION AND ACCUMULATION OF CYTOPLASMIC BETA-CATENIN (XENOPUS) | 16 | 0.48 | 0.82 | 0.709 | 0.908 | 1.000 | 60 | tags=6%, list=0%, signal=6% | |
349 | INOH_IL-1_SIGNALING(THROUGH_IKK-NFKB_CASCADE)(CANONICAL) | 23 | 0.45 | 0.82 | 0.751 | 0.912 | 1.000 | 3117 | tags=35%, list=17%, signal=42% | |
350 | BIOCARTA_REGULATION OF CELL CYCLE PROGRESSION BY PLK3 | 17 | 0.47 | 0.81 | 0.746 | 0.920 | 1.000 | 880 | tags=12%, list=5%, signal=12% | |
351 | REACTOME_TRANS_GOLGI_NETWORK_VESICLE_BUDDING | 15 | 0.47 | 0.81 | 0.754 | 0.918 | 1.000 | 3481 | tags=47%, list=19%, signal=57% | |
352 | REACTOME_INORGANIC_CATION_ANION_SLC_TRANSPORTERS | 12 | 0.49 | 0.81 | 0.753 | 0.918 | 1.000 | 2223 | tags=17%, list=12%, signal=19% | |
353 | REACTOME_CLATHRIN_DERIVED_VESICLE_BUDDING | 15 | 0.47 | 0.81 | 0.749 | 0.916 | 1.000 | 3481 | tags=47%, list=19%, signal=57% | |
354 | BIOCARTA_ENDOCYTOTIC ROLE OF NDK PHOSPHINS AND DYNAMIN | 14 | 0.49 | 0.81 | 0.760 | 0.915 | 1.000 | 3070 | tags=36%, list=16%, signal=43% | |
355 | BIOCARTA_CHAPERONES MODULATE INTERFERON SIGNALING PATHWAY | 16 | 0.48 | 0.81 | 0.751 | 0.913 | 1.000 | 880 | tags=19%, list=5%, signal=20% | |
356 | BIOCARTA_CELL CYCLE: G2/M CHECKPOINT | 19 | 0.46 | 0.81 | 0.749 | 0.914 | 1.000 | 880 | tags=16%, list=5%, signal=17% | |
357 | BIOCARTA_SPROUTY REGULATION OF TYROSINE KINASE SIGNALS | 19 | 0.46 | 0.81 | 0.744 | 0.912 | 1.000 | 2319 | tags=21%, list=12%, signal=24% | |
358 | INOH_G ALPHA S GDP-GTP EXCHANGE SIGNALING | 105 | 0.35 | 0.81 | 0.899 | 0.911 | 1.000 | 2314 | tags=10%, list=12%, signal=12% | |
359 | REACTOME_HOST_INTERACTIONS_OF_HIV_FACTORS | 75 | 0.36 | 0.81 | 0.854 | 0.908 | 1.000 | 2914 | tags=37%, list=16%, signal=44% | |
360 | REACTOME_SMOOTH_MUSCLE_CONTRACTION | 12 | 0.48 | 0.80 | 0.731 | 0.913 | 1.000 | 2984 | tags=25%, list=16%, signal=30% | |
361 | BIOCARTA_PKC-CATALYZED PHOSPHORYLATION OF INHIBITORY PHOSPHOPROTEIN OF MYOSIN PHOSPHATASE | 18 | 0.45 | 0.80 | 0.750 | 0.918 | 1.000 | 56 | tags=6%, list=0%, signal=6% | |
362 | BIOCARTA_CELL CYCLE: G1/S CHECK POINT | 25 | 0.42 | 0.80 | 0.760 | 0.917 | 1.000 | 1706 | tags=28%, list=9%, signal=31% | |
363 | INOH_JAK DEGRADATION SIGNALING | 24 | 0.44 | 0.80 | 0.784 | 0.916 | 1.000 | 1953 | tags=54%, list=10%, signal=60% | |
364 | REACTOME_CELL_JUNCTION_ORGANIZATION | 23 | 0.43 | 0.79 | 0.780 | 0.918 | 1.000 | 594 | tags=9%, list=3%, signal=9% | |
365 | INOH_IL-1 SIGNALING PATHWAY (THROUGH P38 CASCADE) | 24 | 0.43 | 0.79 | 0.775 | 0.917 | 1.000 | 3117 | tags=29%, list=17%, signal=35% | |
366 | BIOCARTA_THE INFORMATION PROCESSING PATHWAY AT THE IFN BETA ENHANCER | 26 | 0.41 | 0.78 | 0.803 | 0.933 | 1.000 | 1739 | tags=19%, list=9%, signal=21% | |
367 | BIOCARTA_HEMOGLOBINS CHAPERONE | 10 | 0.50 | 0.78 | 0.786 | 0.931 | 1.000 | 691 | tags=20%, list=4%, signal=21% | |
368 | INOH_GENE EXPRESSION OF SOCS3 BY STAT DIMER | 26 | 0.41 | 0.78 | 0.828 | 0.931 | 1.000 | 1881 | tags=50%, list=10%, signal=56% | |
369 | BIOCARTA_NERVE GROWTH FACTOR PATHWAY (NGF) | 15 | 0.46 | 0.78 | 0.800 | 0.936 | 1.000 | 2319 | tags=20%, list=12%, signal=23% | |
370 | REACTOME_LATE_PHASE_OF_HIV_LIFE_CYCLE | 63 | 0.36 | 0.77 | 0.890 | 0.936 | 1.000 | 3436 | tags=37%, list=18%, signal=45% | |
371 | CELLMAP_KITRECEPTOR | 49 | 0.37 | 0.77 | 0.865 | 0.934 | 1.000 | 1508 | tags=14%, list=8%, signal=16% | |
372 | INOH_RAP1 ACTIVATION SIGNALING (THROUGH CAMP AND EPAC) | 22 | 0.42 | 0.77 | 0.807 | 0.936 | 1.000 | 353 | tags=9%, list=2%, signal=9% | |
373 | BIOCARTA_TGF BETA SIGNALING PATHWAY | 19 | 0.43 | 0.77 | 0.791 | 0.934 | 1.000 | 1706 | tags=21%, list=9%, signal=23% | |
374 | BIOCARTA_IL-10 ANTI-INFLAMMATORY SIGNALING PATHWAY | 13 | 0.47 | 0.77 | 0.780 | 0.932 | 1.000 | 1958 | tags=23%, list=11%, signal=26% | |
375 | REACTOME_DNA_STRAND_ELONGATION | 23 | 0.41 | 0.77 | 0.832 | 0.937 | 1.000 | 2800 | tags=52%, list=15%, signal=61% | |
376 | INOH_NEGATIVE FEEDBACK REGULATION OF JAK STAT PATHWAY BY (CYTOKINE RECEPTOR DEGRADATION SIGNALING) | 26 | 0.41 | 0.77 | 0.812 | 0.934 | 1.000 | 1881 | tags=50%, list=10%, signal=56% | |
377 | BIOCARTA_INDUCTION OF APOPTOSIS THROUGH DR3 AND DR4/5 DEATH RECEPTORS | 19 | 0.43 | 0.77 | 0.822 | 0.932 | 1.000 | 208 | tags=11%, list=1%, signal=11% | |
378 | NCI_EPHB FORWARD SIGNALING | 35 | 0.38 | 0.76 | 0.867 | 0.943 | 1.000 | 2319 | tags=23%, list=12%, signal=26% | |
379 | REACTOME_GLOBAL_GENOMIC_NER__GG_NER_ | 28 | 0.39 | 0.75 | 0.844 | 0.948 | 1.000 | 2413 | tags=39%, list=13%, signal=45% | |
380 | REACTOME_POLYMERASE_SWITCHING_ON_THE_C_STRAND_OF_THE_TELOMERE | 11 | 0.46 | 0.75 | 0.829 | 0.951 | 1.000 | 3173 | tags=64%, list=17%, signal=77% | |
381 | INOH_B-RAF ACTIVATION SIGNALING | 26 | 0.39 | 0.75 | 0.863 | 0.949 | 1.000 | 564 | tags=12%, list=3%, signal=12% | |
382 | NCI_EPHA2 FORWARD SIGNALING | 17 | 0.42 | 0.74 | 0.838 | 0.953 | 1.000 | 37 | tags=6%, list=0%, signal=6% | |
383 | BIOCARTA_EFFECTS OF CALCINEURIN IN KERATINOCYTE DIFFERENTIATION | 12 | 0.46 | 0.74 | 0.811 | 0.953 | 1.000 | 951 | tags=17%, list=5%, signal=18% | |
384 | BIOCARTA_CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) AND BETA 2 ADRENERGIC RECEPTOR (B2AR) PATHWAY | 17 | 0.43 | 0.74 | 0.834 | 0.952 | 1.000 | 1111 | tags=18%, list=6%, signal=19% | |
385 | REACTOME_LEADING_STRAND_SYNTHESIS | 11 | 0.46 | 0.73 | 0.812 | 0.958 | 1.000 | 3173 | tags=64%, list=17%, signal=77% | |
386 | REACTOME_POLYMERASE_SWITCHING | 11 | 0.46 | 0.73 | 0.832 | 0.963 | 1.000 | 3173 | tags=64%, list=17%, signal=77% | |
387 | BIOCARTA_CCR3 SIGNALING IN EOSINOPHILS | 21 | 0.40 | 0.72 | 0.882 | 0.970 | 1.000 | 2213 | tags=29%, list=12%, signal=32% | |
388 | BIOCARTA_PTEN DEPENDENT CELL CYCLE ARREST AND APOPTOSIS | 15 | 0.42 | 0.72 | 0.859 | 0.972 | 1.000 | 2587 | tags=27%, list=14%, signal=31% | |
389 | BIOCARTA_THE IGF-1 RECEPTOR AND LONGEVITY | 16 | 0.41 | 0.71 | 0.883 | 0.971 | 1.000 | 2319 | tags=25%, list=12%, signal=29% | |
390 | NETPATH_IL1 | 27 | 0.37 | 0.70 | 0.924 | 0.986 | 1.000 | 2930 | tags=30%, list=16%, signal=35% | |
391 | REACTOME_INTERACTIONS_OF_VPR_WITH_HOST_CELLULAR_PROTEINS | 17 | 0.40 | 0.70 | 0.911 | 0.986 | 1.000 | 3478 | tags=35%, list=19%, signal=43% | |
392 | BIOCARTA_GAMMA-AMINOBUTYRIC ACID RECEPTOR LIFE CYCLE PATHWAY | 14 | 0.41 | 0.69 | 0.896 | 0.986 | 1.000 | 441 | tags=7%, list=2%, signal=7% | |
393 | REACTOME_VPR_MEDIATED_NUCLEAR_IMPORT_OF_PICS | 17 | 0.40 | 0.69 | 0.904 | 0.988 | 1.000 | 3478 | tags=35%, list=19%, signal=43% | |
394 | REACTOME_CREB_PHOPHORYLATION_THROUGH_THE_ACTIVATION_OF_RAS | 15 | 0.40 | 0.69 | 0.908 | 0.987 | 1.000 | 2356 | tags=27%, list=13%, signal=31% | |
395 | REACTOME_TOLL_RECEPTOR_CASCADES | 26 | 0.36 | 0.68 | 0.944 | 0.989 | 1.000 | 896 | tags=12%, list=5%, signal=12% | |
396 | REACTOME_MEMBRANE_TRAFFICKING | 26 | 0.36 | 0.68 | 0.933 | 0.988 | 1.000 | 3483 | tags=42%, list=19%, signal=52% | |
397 | REACTOME_AMINE_LIGAND_BINDING_RECEPTORS | 12 | 0.41 | 0.68 | 0.900 | 0.986 | 1.000 | 2881 | tags=8%, list=15%, signal=10% | |
398 | BIOCARTA_DOUBLE STRANDED RNA INDUCED GENE EXPRESSION | 12 | 0.41 | 0.68 | 0.898 | 0.984 | 1.000 | 880 | tags=17%, list=5%, signal=17% | |
399 | INOH_TOLL-LIKE RECEPTOR SIGNALING PATHWAY (THROUGH JNK CASCADE)(CANONICAL) | 23 | 0.37 | 0.68 | 0.930 | 0.983 | 1.000 | 843 | tags=13%, list=5%, signal=14% | |
400 | NCI_VEGFR3 SIGNALING IN LYMPHATIC ENDOTHELIUM | 22 | 0.37 | 0.68 | 0.923 | 0.981 | 1.000 | 2319 | tags=18%, list=12%, signal=21% | |
401 | REACTOME_CLASS_B_2__SECRETIN_FAMILY_RECEPTORS_ | 23 | 0.36 | 0.67 | 0.939 | 0.983 | 1.000 | 1003 | tags=4%, list=5%, signal=5% | |
402 | BIOCARTA_VISUAL SIGNAL TRANSDUCTION | 13 | 0.41 | 0.66 | 0.898 | 0.984 | 1.000 | 1561 | tags=15%, list=8%, signal=17% | |
403 | BIOCARTA_CASPASE CASCADE IN APOPTOSIS | 21 | 0.36 | 0.66 | 0.960 | 0.983 | 1.000 | 2211 | tags=19%, list=12%, signal=22% | |
404 | REACTOME_NUCLEAR_IMPORT_OF_REV_PROTEIN | 17 | 0.38 | 0.65 | 0.941 | 0.990 | 1.000 | 2914 | tags=29%, list=16%, signal=35% | |
405 | NCI_NONGENOTROPIC ANDROGEN SIGNALING | 24 | 0.35 | 0.65 | 0.961 | 0.989 | 1.000 | 2213 | tags=17%, list=12%, signal=19% | |
406 | REACTOME_SIGNALLING_TO_ERKS | 13 | 0.39 | 0.64 | 0.925 | 0.988 | 1.000 | 1667 | tags=15%, list=9%, signal=17% | |
407 | REACTOME_NCAM_SIGNALING_FOR_NEURITE_OUT_GROWTH | 20 | 0.35 | 0.64 | 0.950 | 0.986 | 1.000 | 2213 | tags=20%, list=12%, signal=23% | |
408 | INOH_RAF ACTIVATION SIGNALING (THROUGH GRB2 AND SOS) | 11 | 0.39 | 0.63 | 0.919 | 0.988 | 1.000 | 3424 | tags=45%, list=18%, signal=56% | |
409 | REACTOME_FORMATION_OF_INCISION_COMPLEX_IN_GG_NER | 17 | 0.36 | 0.63 | 0.950 | 0.986 | 1.000 | 2413 | tags=35%, list=13%, signal=41% | |
410 | REACTOME_SIGNALLING_TO_RAS | 12 | 0.39 | 0.63 | 0.922 | 0.984 | 1.000 | 1667 | tags=17%, list=9%, signal=18% | |
411 | REACTOME_DUAL_INCISION_REACTION_IN_GG_NER | 17 | 0.36 | 0.63 | 0.962 | 0.983 | 1.000 | 2413 | tags=35%, list=13%, signal=41% | |
412 | BIOCARTA_ROLE OF ERK5 IN NEURONAL SURVIVAL PATHWAY | 24 | 0.33 | 0.61 | 0.986 | 0.990 | 1.000 | 2621 | tags=21%, list=14%, signal=24% | |
413 | BIOCARTA_ERK1/ERK2 MAPK SIGNALING PATHWAY | 20 | 0.34 | 0.61 | 0.978 | 0.988 | 1.000 | 2319 | tags=20%, list=12%, signal=23% | |
414 | REACTOME_MITOCHONDRIAL_FATTY_ACID_BETA_OXIDATION | 10 | 0.38 | 0.60 | 0.949 | 0.988 | 1.000 | 1345 | tags=20%, list=7%, signal=22% | |
415 | REACTOME_RNA_POLYMERASE_III_TRANSCRIPTION | 16 | 0.34 | 0.59 | 0.979 | 0.987 | 1.000 | 3345 | tags=44%, list=18%, signal=53% | |
416 | NCI_ARF1 PATHWAY | 13 | 0.34 | 0.57 | 0.969 | 0.989 | 1.000 | 3070 | tags=46%, list=16%, signal=55% |