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 | REACTOME_GENE_EXPRESSION | Details ... | 145 | -0.65 | -2.40 | 0.000 | 0.000 | 0.000 | 3605 | tags=57%, list=19%, signal=70% |
2 | REACTOME_DNA_REPLICATION | Details ... | 69 | -0.68 | -2.25 | 0.000 | 0.000 | 0.000 | 3325 | tags=64%, list=18%, signal=77% |
3 | REACTOME_LATE_PHASE_OF_HIV_LIFE_CYCLE | Details ... | 63 | -0.69 | -2.22 | 0.000 | 0.000 | 0.000 | 3267 | tags=67%, list=18%, signal=81% |
4 | REACTOME_METABOLISM_OF_NON_CODING_RNA | Details ... | 27 | -0.80 | -2.21 | 0.000 | 0.000 | 0.000 | 2560 | tags=74%, list=14%, signal=86% |
5 | REACTOME_PROCESSING_OF_CAPPED_INTRON_CONTAINING_PRE_MRNA | Details ... | 85 | -0.64 | -2.19 | 0.000 | 0.000 | 0.000 | 2560 | tags=48%, list=14%, signal=56% |
6 | REACTOME_SYNTHESIS_OF_DNA | Details ... | 65 | -0.68 | -2.18 | 0.000 | 0.000 | 0.000 | 3325 | tags=63%, list=18%, signal=77% |
7 | REACTOME_REGULATION_OF_DNA_REPLICATION | Details ... | 49 | -0.70 | -2.18 | 0.000 | 0.000 | 0.000 | 3325 | tags=69%, list=18%, signal=84% |
8 | REACTOME_SNRNP_ASSEMBLY | Details ... | 27 | -0.80 | -2.16 | 0.000 | 0.000 | 0.000 | 2560 | tags=74%, list=14%, signal=86% |
9 | REACTOME_REMOVAL_OF_LICENSING_FACTORS_FROM_ORIGINS | Details ... | 48 | -0.70 | -2.15 | 0.000 | 0.000 | 0.000 | 3325 | tags=69%, list=18%, signal=83% |
10 | REACTOME_ASSEMBLY_OF_THE_PRE_REPLICATIVE_COMPLEX | Details ... | 46 | -0.70 | -2.15 | 0.000 | 0.000 | 0.000 | 3325 | tags=70%, list=18%, signal=84% |
11 | REACTOME_ORC1_REMOVAL_FROM_CHROMATIN | Details ... | 46 | -0.69 | -2.14 | 0.000 | 0.000 | 0.000 | 3325 | tags=67%, list=18%, signal=82% |
12 | REACTOME_M_G1_TRANSITION | Details ... | 46 | -0.70 | -2.13 | 0.000 | 0.000 | 0.000 | 3325 | tags=70%, list=18%, signal=84% |
13 | REACTOME_SWITCHING_OF_ORIGINS_TO_A_POST_REPLICATIVE_STATE | Details ... | 46 | -0.69 | -2.12 | 0.000 | 0.000 | 0.000 | 3325 | tags=67%, list=18%, signal=82% |
14 | REACTOME_FORMATION_AND_MATURATION_OF_MRNA_TRANSCRIPT | Details ... | 102 | -0.61 | -2.11 | 0.000 | 0.000 | 0.000 | 3250 | tags=55%, list=17%, signal=66% |
15 | REACTOME_S_PHASE | Details ... | 74 | -0.64 | -2.09 | 0.000 | 0.000 | 0.000 | 3325 | tags=61%, list=18%, signal=74% |
16 | REACTOME_G2_M_CHECKPOINTS | Details ... | 30 | -0.74 | -2.07 | 0.000 | 0.000 | 0.000 | 3361 | tags=73%, list=18%, signal=89% |
17 | REACTOME_ACTIVATION_OF_ATR_IN_RESPONSE_TO_REPLICATION_STRESS | Details ... | 26 | -0.76 | -2.07 | 0.000 | 0.000 | 0.001 | 3361 | tags=81%, list=18%, signal=98% |
18 | REACTOME_MRNA_SPLICING___MINOR_PATHWAY | Details ... | 28 | -0.76 | -2.07 | 0.000 | 0.000 | 0.001 | 2560 | tags=61%, list=14%, signal=70% |
19 | REACTOME_TRANSPORT_OF_THE_SLBP_DEPENDANT_MATURE_MRNA | Details ... | 19 | -0.80 | -2.06 | 0.000 | 0.000 | 0.001 | 1217 | tags=58%, list=7%, signal=62% |
20 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION | Details ... | 67 | -0.62 | -2.05 | 0.000 | 0.000 | 0.004 | 3407 | tags=60%, list=18%, signal=73% |
21 | REACTOME_NEGATIVE_REGULATION_OF_GLUCOKINASE_BY_GLUCOKINASE_REGULATORY_PROTEIN | 16 | -0.83 | -2.04 | 0.000 | 0.000 | 0.005 | 1182 | tags=56%, list=6%, signal=60% | |
22 | REACTOME_CELL_CYCLE_CHECKPOINTS | 75 | -0.62 | -2.04 | 0.000 | 0.000 | 0.005 | 3361 | tags=61%, list=18%, signal=75% | |
23 | REACTOME_CDT1_ASSOCIATION_WITH_THE_CDC6_ORC_ORIGIN_COMPLEX | 39 | -0.69 | -2.04 | 0.000 | 0.000 | 0.005 | 3325 | tags=67%, list=18%, signal=81% | |
24 | REACTOME_TRANSPORT_OF_MATURE_MRNA_DERIVED_FROM_AN_INTRONLESS_TRANSCRIPT | 19 | -0.79 | -2.04 | 0.002 | 0.000 | 0.005 | 1217 | tags=58%, list=7%, signal=62% | |
25 | REACTOME_HIV_INFECTION | 121 | -0.57 | -2.03 | 0.000 | 0.000 | 0.007 | 3325 | tags=56%, list=18%, signal=68% | |
26 | REACTOME_GLUCOSE_UPTAKE | 22 | -0.78 | -2.03 | 0.000 | 0.000 | 0.007 | 1182 | tags=45%, list=6%, signal=48% | |
27 | REACTOME_CELL_CYCLE__MITOTIC | 143 | -0.55 | -2.03 | 0.000 | 0.000 | 0.008 | 3377 | tags=46%, list=18%, signal=56% | |
28 | REACTOME_TRANSPORT_OF_MATURE_MRNAS_DERIVED_FROM_INTRONLESS_TRANSCRIPTS | 20 | -0.78 | -2.03 | 0.000 | 0.000 | 0.008 | 1217 | tags=55%, list=7%, signal=59% | |
29 | REACTOME_VPR_MEDIATED_NUCLEAR_IMPORT_OF_PICS | 17 | -0.81 | -2.02 | 0.000 | 0.000 | 0.009 | 1182 | tags=59%, list=6%, signal=63% | |
30 | REACTOME_TRANSPORT_OF_THE_SLBP_INDEPENDENT_MATURE_MRNA | 18 | -0.82 | -2.02 | 0.000 | 0.000 | 0.009 | 1217 | tags=61%, list=7%, signal=65% | |
31 | REACTOME_INFLUENZA_LIFE_CYCLE | 111 | -0.57 | -2.02 | 0.000 | 0.000 | 0.009 | 2560 | tags=37%, list=14%, signal=43% | |
32 | REACTOME_G1_S_TRANSITION | 75 | -0.60 | -2.02 | 0.000 | 0.000 | 0.010 | 3325 | tags=59%, list=18%, signal=71% | |
33 | REACTOME_HIV_LIFE_CYCLE | 72 | -0.63 | -2.02 | 0.000 | 0.000 | 0.011 | 2798 | tags=56%, list=15%, signal=65% | |
34 | REACTOME_RNA_POLYMERASE_II_HIV_1_PROMOTER_ESCAPE | 32 | -0.70 | -2.02 | 0.000 | 0.000 | 0.012 | 2798 | tags=63%, list=15%, signal=73% | |
35 | REACTOME_ACTIVATION_OF_THE_PRE_REPLICATIVE_COMPLEX | 22 | -0.77 | -2.01 | 0.000 | 0.000 | 0.013 | 3258 | tags=73%, list=18%, signal=88% | |
36 | REACTOME_TRANSCRIPTION_COUPLED_NER__TC_NER_ | 33 | -0.71 | -2.01 | 0.000 | 0.000 | 0.014 | 2458 | tags=58%, list=13%, signal=66% | |
37 | REACTOME_TRANSPORT_OF_MATURE_MRNA_DERIVED_FROM_AN_INTRON_CONTAINING_TRANSCRIPT | 31 | -0.72 | -2.01 | 0.000 | 0.000 | 0.014 | 2334 | tags=55%, list=13%, signal=63% | |
38 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION_INITIATION_AND_PROMOTER_CLEARANCE | 32 | -0.70 | -2.01 | 0.000 | 0.000 | 0.014 | 2798 | tags=63%, list=15%, signal=73% | |
39 | REACTOME_RNA_POLYMERASE_II_PROMOTER_ESCAPE | 32 | -0.70 | -2.01 | 0.000 | 0.000 | 0.016 | 2798 | tags=63%, list=15%, signal=73% | |
40 | REACTOME_TRANSPORT_OF_RIBONUCLEOPROTEINS_INTO_THE_HOST_NUCLEUS | 17 | -0.81 | -2.00 | 0.000 | 0.000 | 0.017 | 1182 | tags=59%, list=6%, signal=63% | |
41 | REACTOME_HIV_1_TRANSCRIPTION_INITIATION | 32 | -0.70 | -2.00 | 0.000 | 0.000 | 0.017 | 2798 | tags=63%, list=15%, signal=73% | |
42 | REACTOME_TRANSCRIPTION_OF_THE_HIV_GENOME | 44 | -0.66 | -2.00 | 0.000 | 0.000 | 0.018 | 3250 | tags=66%, list=17%, signal=80% | |
43 | REACTOME_MRNA_SPLICING___MAJOR_PATHWAY | 67 | -0.61 | -2.00 | 0.000 | 0.000 | 0.019 | 3045 | tags=49%, list=16%, signal=59% | |
44 | REACTOME_INTERACTIONS_OF_REV_WITH_HOST_CELLULAR_PROTEINS | 20 | -0.78 | -2.00 | 0.000 | 0.000 | 0.021 | 1182 | tags=55%, list=6%, signal=59% | |
45 | REACTOME_HIV_1_TRANSCRIPTION_PRE_INITIATION | 32 | -0.70 | -1.99 | 0.000 | 0.000 | 0.022 | 2798 | tags=63%, list=15%, signal=73% | |
46 | REACTOME_TRANSPORT_OF_MATURE_TRANSCRIPT_TO_CYTOPLASM | 33 | -0.70 | -1.99 | 0.000 | 0.000 | 0.022 | 3684 | tags=67%, list=20%, signal=83% | |
47 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION_INITIATION | 32 | -0.70 | -1.99 | 0.000 | 0.000 | 0.022 | 2798 | tags=63%, list=15%, signal=73% | |
48 | REACTOME_INTERACTIONS_OF_VPR_WITH_HOST_CELLULAR_PROTEINS | 17 | -0.81 | -1.99 | 0.000 | 0.000 | 0.022 | 1182 | tags=59%, list=6%, signal=63% | |
49 | REACTOME_UBIQUITIN_DEPENDENT_DEGRADATION_OF_CYCLIN_D1 | 36 | -0.69 | -1.98 | 0.000 | 0.000 | 0.025 | 4049 | tags=75%, list=22%, signal=96% | |
50 | REACTOME_INFLUENZA_INFECTION | 115 | -0.55 | -1.98 | 0.000 | 0.000 | 0.027 | 2560 | tags=37%, list=14%, signal=42% | |
51 | REACTOME_ELONGATION_OF_INTRON_CONTAINING_TRANSCRIPTS_AND_CO_TRANSCRIPTIONAL_MRNA_SPLICING | 86 | -0.58 | -1.98 | 0.000 | 0.000 | 0.027 | 2560 | tags=47%, list=14%, signal=54% | |
52 | HUMANCYC_SUPERPATHWAY OF HISTIDINE, PURINE, AND PYRIMIDINE BIOSYNTHESIS | 33 | -0.69 | -1.97 | 0.000 | 0.000 | 0.029 | 654 | tags=48%, list=4%, signal=50% | |
53 | REACTOME_UBIQUITIN_DEPENDENT_DEGRADATION_OF_CYCLIN_D | 36 | -0.69 | -1.97 | 0.000 | 0.001 | 0.030 | 4049 | tags=75%, list=22%, signal=96% | |
54 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION_PRE_INITIATION | 32 | -0.70 | -1.97 | 0.000 | 0.001 | 0.032 | 2798 | tags=63%, list=15%, signal=73% | |
55 | REACTOME_TRNA_AMINOACYLATION | 18 | -0.79 | -1.96 | 0.000 | 0.001 | 0.032 | 2348 | tags=67%, list=13%, signal=76% | |
56 | REACTOME_ELONGATION_AND_PROCESSING_OF_CAPPED_TRANSCRIPTS | 86 | -0.58 | -1.95 | 0.000 | 0.001 | 0.037 | 2560 | tags=47%, list=14%, signal=54% | |
57 | REACTOME_CYTOSOLIC_TRNA_AMINOACYLATION | 14 | -0.83 | -1.95 | 0.000 | 0.001 | 0.037 | 968 | tags=57%, list=5%, signal=60% | |
58 | REACTOME_AUTODEGRADATION_OF_CDH1_BY_CDH1_APC_C | 38 | -0.67 | -1.95 | 0.000 | 0.001 | 0.041 | 4049 | tags=71%, list=22%, signal=91% | |
59 | REACTOME_MRNA_SPLICING | 67 | -0.61 | -1.95 | 0.000 | 0.001 | 0.041 | 3045 | tags=49%, list=16%, signal=59% | |
60 | REACTOME_AUTODEGRADATION_OF_THE_E3_UBIQUITIN_LIGASE_COP1 | 36 | -0.66 | -1.95 | 0.000 | 0.001 | 0.042 | 4049 | tags=72%, list=22%, signal=92% | |
61 | REACTOME_EXPORT_OF_VIRAL_RIBONUCLEOPROTEINS_FROM_NUCLEUS | 17 | -0.79 | -1.95 | 0.000 | 0.001 | 0.042 | 1182 | tags=53%, list=6%, signal=56% | |
62 | REACTOME_NUCLEAR_IMPORT_OF_REV_PROTEIN | 17 | -0.81 | -1.95 | 0.000 | 0.001 | 0.042 | 1182 | tags=59%, list=6%, signal=63% | |
63 | REACTOME_REGULATION_OF_ACTIVATED_PAK_2P34_BY_PROTEASOME_MEDIATED_DEGRADATION1 | 34 | -0.67 | -1.94 | 0.000 | 0.001 | 0.043 | 4049 | tags=74%, list=22%, signal=94% | |
64 | REACTOME_REV_MEDIATED_NUCLEAR_EXPORT_OF_HIV_1_RNA | 19 | -0.78 | -1.94 | 0.000 | 0.001 | 0.047 | 1182 | tags=53%, list=6%, signal=56% | |
65 | REACTOME_CDK_MEDIATED_PHOSPHORYLATION_AND_REMOVAL_OF_CDC6 | 35 | -0.67 | -1.94 | 0.002 | 0.001 | 0.048 | 4049 | tags=74%, list=22%, signal=95% | |
66 | REACTOME_NUCLEOTIDE_EXCISION_REPAIR | 37 | -0.67 | -1.93 | 0.000 | 0.001 | 0.051 | 2458 | tags=51%, list=13%, signal=59% | |
67 | REACTOME_APC_C_CDH1_MEDIATED_DEGRADATION_OF_CDC20_AND_OTHER_APC_C_CDH1_TARGETED_PROTEINS_IN_LATE_MITOSIS_EARLY_G1 | 39 | -0.65 | -1.93 | 0.000 | 0.001 | 0.054 | 4049 | tags=69%, list=22%, signal=88% | |
68 | REACTOME_P53_INDEPENDENT_G1_S_DNA_DAMAGE_CHECKPOINT | 35 | -0.67 | -1.93 | 0.002 | 0.001 | 0.054 | 4049 | tags=74%, list=22%, signal=95% | |
69 | HUMANCYC_DE NOVO BIOSYNTHESIS OF PYRIMIDINE RIBONUCLEOTIDES | 11 | -0.87 | -1.93 | 0.000 | 0.001 | 0.060 | 654 | tags=73%, list=4%, signal=75% | |
70 | REACTOME_GLUCOSE_REGULATION_OF_INSULIN_SECRETION | 90 | -0.56 | -1.92 | 0.000 | 0.001 | 0.061 | 3758 | tags=57%, list=20%, signal=71% | |
71 | REACTOME_NEP_NS2_INTERACTS_WITH_THE_CELLULAR_EXPORT_MACHINERY | 17 | -0.79 | -1.92 | 0.000 | 0.001 | 0.063 | 1182 | tags=53%, list=6%, signal=56% | |
72 | REACTOME_METABOLISM_OF_AMINO_ACIDS | 106 | -0.55 | -1.92 | 0.000 | 0.001 | 0.066 | 2709 | tags=38%, list=15%, signal=44% | |
73 | REACTOME_UBIQUITIN_MEDIATED_DEGRADATION_OF_PHOSPHORYLATED_CDC25A | 35 | -0.67 | -1.92 | 0.000 | 0.001 | 0.070 | 4049 | tags=74%, list=22%, signal=95% | |
74 | REACTOME_CDC20_PHOSPHO_APC_C_MEDIATED_DEGRADATION_OF_CYCLIN_A | 42 | -0.64 | -1.92 | 0.000 | 0.001 | 0.071 | 4049 | tags=67%, list=22%, signal=85% | |
75 | REACTOME_SIGNALING_BY_WNT | 37 | -0.65 | -1.91 | 0.002 | 0.001 | 0.076 | 4163 | tags=73%, list=22%, signal=94% | |
76 | REACTOME_P53_INDEPENDENT_DNA_DAMAGE_RESPONSE | 35 | -0.67 | -1.91 | 0.000 | 0.001 | 0.077 | 4049 | tags=74%, list=22%, signal=95% | |
77 | BIOCARTA_ROLE OF BRCA1 BRCA2 AND ATR IN CANCER SUSCEPTIBILITY | 21 | -0.74 | -1.91 | 0.002 | 0.001 | 0.078 | 3463 | tags=67%, list=19%, signal=82% | |
78 | REACTOME_ORNITHINE_AND_PROLINE_METABOLISM | 46 | -0.62 | -1.91 | 0.000 | 0.001 | 0.083 | 4049 | tags=63%, list=22%, signal=80% | |
79 | REACTOME_VPU_MEDIATED_DEGRADATION_OF_CD4 | 35 | -0.66 | -1.91 | 0.000 | 0.001 | 0.087 | 4049 | tags=71%, list=22%, signal=91% | |
80 | REACTOME_SCF_BETA_TRCP_MEDIATED_DEGRADATION_OF_EMI1 | 35 | -0.66 | -1.91 | 0.000 | 0.001 | 0.097 | 4163 | tags=74%, list=22%, signal=96% | |
81 | REACTOME_REGULATION_OF_APC_C_ACTIVATORS_BETWEEN_G1_S_AND_EARLY_ANAPHASE | 46 | -0.62 | -1.90 | 0.000 | 0.001 | 0.099 | 4163 | tags=65%, list=22%, signal=84% | |
82 | REACTOME_DNA_REPAIR | 66 | -0.58 | -1.90 | 0.000 | 0.001 | 0.102 | 2122 | tags=39%, list=11%, signal=44% | |
83 | REACTOME_REGULATION_OF_ORNITHINE_DECARBOXYLASE__ODC_ | 38 | -0.64 | -1.90 | 0.000 | 0.001 | 0.103 | 4049 | tags=68%, list=22%, signal=87% | |
84 | REACTOME_HOST_INTERACTIONS_OF_HIV_FACTORS | 75 | -0.56 | -1.89 | 0.000 | 0.001 | 0.121 | 3325 | tags=55%, list=18%, signal=66% | |
85 | REACTOME_REGULATION_OF_ACTIVATED_PAK_2P34_BY_PROTEASOME_MEDIATED_DEGRADATION | 35 | -0.67 | -1.89 | 0.000 | 0.001 | 0.130 | 4049 | tags=74%, list=22%, signal=95% | |
86 | REACTOME_MRNA_CAPPING | 21 | -0.73 | -1.89 | 0.000 | 0.001 | 0.132 | 2458 | tags=67%, list=13%, signal=77% | |
87 | REACTOME_ORNITHINE_METABOLISM | 43 | -0.62 | -1.87 | 0.000 | 0.002 | 0.161 | 4049 | tags=63%, list=22%, signal=80% | |
88 | REACTOME_APC_C_MEDIATED_DEGRADATION_OF_CELL_CYCLE_PROTEINS | 47 | -0.60 | -1.87 | 0.000 | 0.002 | 0.183 | 4163 | tags=64%, list=22%, signal=82% | |
89 | REACTOME_RNA_POL_II_CTD_PHOSPHORYLATION_AND_INTERACTION_WITH_CE | 20 | -0.72 | -1.86 | 0.004 | 0.003 | 0.229 | 2458 | tags=65%, list=13%, signal=75% | |
90 | REACTOME_FORMATION_OF_TRANSCRIPTION_COUPLED_NER__TC_NER__REPAIR_COMPLEX | 19 | -0.73 | -1.85 | 0.000 | 0.003 | 0.243 | 2458 | tags=63%, list=13%, signal=73% | |
91 | REACTOME_REGULATION_OF_APOPTOSIS | 36 | -0.64 | -1.85 | 0.000 | 0.003 | 0.248 | 4049 | tags=72%, list=22%, signal=92% | |
92 | REACTOME_DUAL_INCISION_REACTION_IN_TC_NER | 19 | -0.73 | -1.85 | 0.002 | 0.003 | 0.255 | 2458 | tags=63%, list=13%, signal=73% | |
93 | REACTOME_METABOLISM_OF_WATER_SOLUBLE_VITAMINS_AND_COFACTORS | 19 | -0.71 | -1.85 | 0.002 | 0.003 | 0.263 | 1462 | tags=37%, list=8%, signal=40% | |
94 | REACTOME_FORMATION_OF_THE_HIV_1_EARLY_ELONGATION_COMPLEX | 22 | -0.71 | -1.84 | 0.000 | 0.003 | 0.266 | 2458 | tags=64%, list=13%, signal=73% | |
95 | BIOCARTA_CDK REGULATION OF DNA REPLICATION | 18 | -0.73 | -1.84 | 0.002 | 0.003 | 0.275 | 3258 | tags=78%, list=18%, signal=94% | |
96 | REACTOME_FORMATION_OF_THE_EARLY_ELONGATION_COMPLEX | 22 | -0.71 | -1.84 | 0.002 | 0.003 | 0.277 | 2458 | tags=64%, list=13%, signal=73% | |
97 | REACTOME_INTEGRATION_OF_ENERGY_METABOLISM | 109 | -0.52 | -1.84 | 0.000 | 0.003 | 0.309 | 3758 | tags=51%, list=20%, signal=64% | |
98 | REACTOME_METABOLISM_OF_VITAMINS_AND_COFACTORS | 19 | -0.71 | -1.83 | 0.000 | 0.004 | 0.337 | 1462 | tags=37%, list=8%, signal=40% | |
99 | REACTOME_TRANSCRIPTION | 92 | -0.54 | -1.83 | 0.000 | 0.004 | 0.340 | 3250 | tags=49%, list=17%, signal=59% | |
100 | REACTOME_TRANSLATION | 63 | -0.57 | -1.83 | 0.000 | 0.004 | 0.340 | 2256 | tags=33%, list=12%, signal=38% | |
101 | REACTOME_APC_C_CDC20_MEDIATED_DEGRADATION_OF_MITOTIC_PROTEINS | 44 | -0.61 | -1.82 | 0.002 | 0.004 | 0.360 | 4049 | tags=64%, list=22%, signal=81% | |
102 | REACTOME_DIABETES_PATHWAYS | 159 | -0.49 | -1.82 | 0.000 | 0.004 | 0.373 | 3781 | tags=40%, list=20%, signal=49% | |
103 | REACTOME_STABILIZATION_OF_P53 | 37 | -0.63 | -1.82 | 0.000 | 0.004 | 0.377 | 4049 | tags=70%, list=22%, signal=90% | |
104 | REACTOME_ABORTIVE_ELONGATION_OF_HIV_1_TRANSCRIPT_IN_THE_ABSENCE_OF_TAT | 14 | -0.78 | -1.82 | 0.002 | 0.004 | 0.386 | 2122 | tags=64%, list=11%, signal=73% | |
105 | REACTOME_ACTIVATION_OF_APC_C_AND_APC_C_CDC20_MEDIATED_DEGRADATION_OF_MITOTIC_PROTEINS | 45 | -0.60 | -1.81 | 0.000 | 0.004 | 0.392 | 4049 | tags=62%, list=22%, signal=79% | |
106 | REACTOME_REGULATION_OF_INSULIN_SECRETION | 101 | -0.52 | -1.81 | 0.000 | 0.005 | 0.416 | 3758 | tags=52%, list=20%, signal=65% | |
107 | REACTOME_RNA_POL_II_CTD_PHOSPHORYLATION_AND_INTERACTION_WITH_CE1 | 20 | -0.72 | -1.81 | 0.000 | 0.005 | 0.418 | 2458 | tags=65%, list=13%, signal=75% | |
108 | REACTOME_METABOLISM_OF_PROTEINS | 98 | -0.52 | -1.79 | 0.000 | 0.006 | 0.488 | 2256 | tags=32%, list=12%, signal=36% | |
109 | REACTOME_VIF_MEDIATED_DEGRADATION_OF_APOBEC3G | 37 | -0.63 | -1.79 | 0.000 | 0.006 | 0.494 | 4049 | tags=70%, list=22%, signal=90% | |
110 | REACTOME_CAP_DEPENDENT_TRANSLATION_INITIATION | 58 | -0.56 | -1.79 | 0.000 | 0.006 | 0.505 | 2256 | tags=31%, list=12%, signal=35% | |
111 | REACTOME_ELECTRON_TRANSPORT_CHAIN | 53 | -0.56 | -1.78 | 0.000 | 0.007 | 0.574 | 3889 | tags=55%, list=21%, signal=69% | |
112 | REACTOME_EUKARYOTIC_TRANSLATION_INITIATION | 58 | -0.56 | -1.77 | 0.002 | 0.007 | 0.589 | 2256 | tags=31%, list=12%, signal=35% | |
113 | REACTOME_VIRAL_MESSENGER_RNA_SYNTHESIS | 43 | -0.58 | -1.77 | 0.002 | 0.007 | 0.615 | 3684 | tags=53%, list=20%, signal=67% | |
114 | REACTOME_DNA_STRAND_ELONGATION | 23 | -0.66 | -1.76 | 0.007 | 0.008 | 0.636 | 3258 | tags=61%, list=18%, signal=74% | |
115 | HUMANCYC_SALVAGE PATHWAYS OF PYRIMIDINE RIBONUCLEOTIDES | 12 | -0.75 | -1.76 | 0.010 | 0.008 | 0.653 | 1572 | tags=50%, list=8%, signal=55% | |
116 | REACTOME_INFLUENZA_VIRAL_RNA_TRANSCRIPTION_AND_REPLICATION | 90 | -0.51 | -1.75 | 0.000 | 0.009 | 0.688 | 3077 | tags=36%, list=17%, signal=42% | |
117 | HUMANCYC_PURINE NUCLEOTIDES DE NOVO BIOSYNTHESIS I | 25 | -0.66 | -1.75 | 0.002 | 0.009 | 0.694 | 654 | tags=48%, list=4%, signal=50% | |
118 | REACTOME_HIV_1_TRANSCRIPTION_ELONGATION | 28 | -0.63 | -1.75 | 0.006 | 0.009 | 0.701 | 2458 | tags=57%, list=13%, signal=66% | |
119 | REACTOME_FORMATION_OF_RNA_POL_II_ELONGATION_COMPLEX_ | 29 | -0.62 | -1.75 | 0.008 | 0.009 | 0.711 | 2458 | tags=55%, list=13%, signal=63% | |
120 | HUMANCYC_SERINE-ISOCITRATE LYASE PATHWAY | 16 | -0.72 | -1.75 | 0.002 | 0.009 | 0.715 | 2952 | tags=56%, list=16%, signal=67% | |
121 | REACTOME_FORMATION_OF_HIV_1_ELONGATION_COMPLEX_CONTAINING_HIV_1_TAT | 28 | -0.63 | -1.75 | 0.000 | 0.009 | 0.722 | 2458 | tags=57%, list=13%, signal=66% | |
122 | REACTOME_TAT_MEDIATED_ELONGATION_OF_THE_HIV_1_TRANSCRIPT | 28 | -0.63 | -1.74 | 0.008 | 0.010 | 0.737 | 2458 | tags=57%, list=13%, signal=66% | |
123 | REACTOME_CYCLIN_E_ASSOCIATED_EVENTS_DURING_G1_S_TRANSITION_ | 44 | -0.57 | -1.74 | 0.004 | 0.010 | 0.744 | 4163 | tags=68%, list=22%, signal=88% | |
124 | HUMANCYC_NAD/NADH PHOSPHORYLATION AND DEPHOSPHORYLATION | 30 | -0.61 | -1.74 | 0.006 | 0.010 | 0.756 | 3758 | tags=53%, list=20%, signal=67% | |
125 | REACTOME_CITRIC_ACID_CYCLE__TCA_CYCLE_ | 12 | -0.76 | -1.73 | 0.004 | 0.010 | 0.783 | 2357 | tags=67%, list=13%, signal=76% | |
126 | REACTOME_REPAIR_SYNTHESIS_OF_PATCH__27_30_BASES_LONG__BY_DNA_POLYMERASE | 13 | -0.75 | -1.73 | 0.009 | 0.011 | 0.795 | 1847 | tags=54%, list=10%, signal=60% | |
127 | BIOCARTA_TUMOR SUPPRESSOR ARF INHIBITS RIBOSOMAL BIOGENESIS | 20 | -0.68 | -1.73 | 0.008 | 0.011 | 0.808 | 3070 | tags=45%, list=16%, signal=54% | |
128 | REACTOME_PYRIMIDINE_METABOLISM | 17 | -0.69 | -1.72 | 0.006 | 0.011 | 0.808 | 1338 | tags=47%, list=7%, signal=51% | |
129 | REACTOME_MRNA_PROCESSING | 24 | -0.65 | -1.72 | 0.002 | 0.012 | 0.833 | 2458 | tags=67%, list=13%, signal=77% | |
130 | REACTOME_E2F_MEDIATED_REGULATION_OF_DNA_REPLICATION | 21 | -0.67 | -1.72 | 0.008 | 0.012 | 0.833 | 2288 | tags=48%, list=12%, signal=54% | |
131 | REACTOME_RESOLUTION_OF_ABASIC_SITES__AP_SITES_ | 14 | -0.73 | -1.72 | 0.002 | 0.012 | 0.839 | 1668 | tags=50%, list=9%, signal=55% | |
132 | REACTOME_CYCLIN_A_CDK2_ASSOCIATED_EVENTS_AT_S_PHASE_ENTRY | 43 | -0.56 | -1.72 | 0.000 | 0.012 | 0.843 | 4163 | tags=67%, list=22%, signal=87% | |
133 | REACTOME_CHAPERONIN_MEDIATED_PROTEIN_FOLDING | 10 | -0.80 | -1.71 | 0.000 | 0.013 | 0.866 | 2222 | tags=70%, list=12%, signal=79% | |
134 | REACTOME_REPAIR_SYNTHESIS_FOR_GAP_FILLING_BY_DNA_POLYMERASE_IN_TC_NER | 13 | -0.75 | -1.70 | 0.002 | 0.014 | 0.886 | 1847 | tags=54%, list=10%, signal=60% | |
135 | REACTOME_GAP_FILLING_DNA_REPAIR_SYNTHESIS_AND_LIGATION_IN_TC_NER | 14 | -0.72 | -1.70 | 0.006 | 0.014 | 0.887 | 1847 | tags=50%, list=10%, signal=55% | |
136 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION_ELONGATION | 29 | -0.62 | -1.70 | 0.010 | 0.014 | 0.887 | 2458 | tags=55%, list=13%, signal=63% | |
137 | REACTOME_COOPERATION_OF_PREFOLDIN_AND_TRIC_CCT__IN_ACTIN_AND_TUBULIN_FOLDING | 10 | -0.80 | -1.70 | 0.008 | 0.014 | 0.889 | 2222 | tags=70%, list=12%, signal=79% | |
138 | REACTOME_GAP_FILLING_DNA_REPAIR_SYNTHESIS_AND_LIGATION_IN_GG_NER | 14 | -0.72 | -1.70 | 0.004 | 0.014 | 0.890 | 1847 | tags=50%, list=10%, signal=55% | |
139 | REACTOME_GLOBAL_GENOMIC_NER__GG_NER_ | 28 | -0.62 | -1.69 | 0.002 | 0.015 | 0.909 | 2458 | tags=46%, list=13%, signal=53% | |
140 | REACTOME_BASE_EXCISION_REPAIR | 14 | -0.73 | -1.69 | 0.008 | 0.015 | 0.911 | 1668 | tags=50%, list=9%, signal=55% | |
141 | REACTOME_PYRUVATE_METABOLISM_AND_TCA_CYCLE | 17 | -0.70 | -1.69 | 0.006 | 0.015 | 0.913 | 4093 | tags=71%, list=22%, signal=90% | |
142 | REACTOME_TELOMERE_C_STRAND__LAGGING_STRAND__SYNTHESIS | 18 | -0.68 | -1.68 | 0.008 | 0.016 | 0.931 | 1847 | tags=44%, list=10%, signal=49% | |
143 | REACTOME_REGULATORY_RNA_PATHWAYS | 10 | -0.79 | -1.68 | 0.006 | 0.017 | 0.945 | 2430 | tags=70%, list=13%, signal=80% | |
144 | REACTOME_GLUCOSE_METABOLISM | 54 | -0.54 | -1.67 | 0.004 | 0.018 | 0.949 | 3380 | tags=41%, list=18%, signal=50% | |
145 | REACTOME_SCF_SKP2__MEDIATED_DEGRADATION_OF_P27_P21 | 37 | -0.57 | -1.64 | 0.008 | 0.024 | 0.979 | 4163 | tags=73%, list=22%, signal=94% | |
146 | REACTOME_G1_S_DNA_DAMAGE_CHECKPOINTS | 40 | -0.55 | -1.64 | 0.002 | 0.024 | 0.983 | 4049 | tags=70%, list=22%, signal=89% | |
147 | HUMANCYC_GLYCINE BETAINE DEGRADATION | 10 | -0.75 | -1.64 | 0.015 | 0.026 | 0.987 | 232 | tags=20%, list=1%, signal=20% | |
148 | REACTOME_LAGGING_STRAND_SYNTHESIS | 16 | -0.67 | -1.63 | 0.013 | 0.026 | 0.992 | 1847 | tags=44%, list=10%, signal=49% | |
149 | NCI_BARD1 SIGNALING EVENTS | 26 | -0.60 | -1.63 | 0.014 | 0.026 | 0.992 | 2932 | tags=46%, list=16%, signal=55% | |
150 | REACTOME_EXTENSION_OF_TELOMERES | 19 | -0.64 | -1.63 | 0.014 | 0.027 | 0.992 | 1847 | tags=42%, list=10%, signal=47% | |
151 | REACTOME_METABOLISM_OF_NUCLEOTIDES | 62 | -0.51 | -1.63 | 0.010 | 0.027 | 0.992 | 3504 | tags=55%, list=19%, signal=67% | |
152 | REACTOME_P53_DEPENDENT_G1_DNA_DAMAGE_RESPONSE | 39 | -0.55 | -1.62 | 0.008 | 0.028 | 0.992 | 4049 | tags=69%, list=22%, signal=88% | |
153 | REACTOME_POST_ELONGATION_PROCESSING_OF_THE_TRANSCRIPT | 23 | -0.61 | -1.62 | 0.015 | 0.028 | 0.993 | 4025 | tags=61%, list=22%, signal=78% | |
154 | REACTOME_DEADENYLATION_DEPENDENT_MRNA_DECAY | 15 | -0.66 | -1.62 | 0.026 | 0.028 | 0.993 | 1806 | tags=60%, list=10%, signal=66% | |
155 | REACTOME_P53_DEPENDENT_G1_S_DNA_DAMAGE_CHECKPOINT | 39 | -0.55 | -1.62 | 0.006 | 0.028 | 0.993 | 4049 | tags=69%, list=22%, signal=88% | |
156 | REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION_TERMINATION | 23 | -0.61 | -1.62 | 0.012 | 0.028 | 0.993 | 4025 | tags=61%, list=22%, signal=78% | |
157 | REACTOME_CLEAVAGE_OF_GROWING_TRANSCRIPT_IN_THE_TERMINATION_REGION_ | 23 | -0.61 | -1.61 | 0.017 | 0.031 | 0.998 | 4025 | tags=61%, list=22%, signal=78% | |
158 | REACTOME_PAUSING_AND_RECOVERY_OF_ELONGATION | 20 | -0.62 | -1.60 | 0.014 | 0.032 | 0.998 | 2122 | tags=50%, list=11%, signal=56% | |
159 | REACTOME_PROTEIN_FOLDING | 13 | -0.69 | -1.60 | 0.031 | 0.032 | 0.998 | 2222 | tags=54%, list=12%, signal=61% | |
160 | HUMANCYC_SUPERPATHWAY OF N-ACETYLNEURAMINATE DEGRADATION | 22 | -0.60 | -1.60 | 0.019 | 0.033 | 0.999 | 1193 | tags=32%, list=6%, signal=34% | |
161 | REACTOME_METABOLISM_OF_MRNA | 15 | -0.66 | -1.60 | 0.025 | 0.034 | 0.999 | 1806 | tags=60%, list=10%, signal=66% | |
162 | REACTOME_FORMATION_OF_ATP_BY_CHEMIOSMOTIC_COUPLING | 12 | -0.70 | -1.60 | 0.015 | 0.034 | 0.999 | 3504 | tags=75%, list=19%, signal=92% | |
163 | REACTOME_MRNA_3__END_PROCESSING | 23 | -0.61 | -1.60 | 0.028 | 0.034 | 0.999 | 4025 | tags=61%, list=22%, signal=78% | |
164 | REACTOME_POST_ELONGATION_PROCESSING_OF_INTRON_CONTAINING_PRE_MRNA | 23 | -0.61 | -1.59 | 0.023 | 0.035 | 1.000 | 4025 | tags=61%, list=22%, signal=78% | |
165 | REACTOME_PAUSING_AND_RECOVERY_OF_TAT_MEDIATED_HIV_1_ELONGATION | 19 | -0.63 | -1.59 | 0.027 | 0.036 | 1.000 | 2122 | tags=53%, list=11%, signal=59% | |
166 | REACTOME_TELOMERE_MAINTENANCE | 22 | -0.60 | -1.59 | 0.024 | 0.036 | 1.000 | 1847 | tags=36%, list=10%, signal=40% | |
167 | REACTOME_RNA_POLYMERASE_I_CHAIN_ELONGATION | 15 | -0.67 | -1.59 | 0.028 | 0.036 | 1.000 | 2726 | tags=60%, list=15%, signal=70% | |
168 | REACTOME_TAT_MEDIATED_HIV_1_ELONGATION_ARREST_AND_RECOVERY_ | 19 | -0.63 | -1.59 | 0.016 | 0.037 | 1.000 | 2122 | tags=53%, list=11%, signal=59% | |
169 | HUMANCYC_TCA CYCLE VARIATION III (EUKARYOTIC) | 16 | -0.67 | -1.58 | 0.031 | 0.037 | 1.000 | 4423 | tags=75%, list=24%, signal=98% | |
170 | REACTOME_POLYMERASE_SWITCHING | 11 | -0.70 | -1.58 | 0.033 | 0.037 | 1.000 | 1404 | tags=45%, list=8%, signal=49% | |
171 | REACTOME_REMOVAL_OF_DNA_PATCH_CONTAINING_ABASIC_RESIDUE | 11 | -0.71 | -1.58 | 0.040 | 0.039 | 1.000 | 1668 | tags=45%, list=9%, signal=50% | |
172 | REACTOME_HIV_1_ELONGATION_ARREST_AND_RECOVERY | 20 | -0.62 | -1.57 | 0.025 | 0.041 | 1.000 | 2122 | tags=50%, list=11%, signal=56% | |
173 | REACTOME_RNA_POLYMERASE_I_TRANSCRIPTION_INITIATION | 15 | -0.65 | -1.57 | 0.013 | 0.041 | 1.000 | 2726 | tags=53%, list=15%, signal=62% | |
174 | REACTOME_ATP_FORMATION | 15 | -0.64 | -1.57 | 0.039 | 0.042 | 1.000 | 4124 | tags=73%, list=22%, signal=94% | |
175 | REACTOME_RNA_POLYMERASE_I_TRANSCRIPTION_TERMINATION | 16 | -0.65 | -1.57 | 0.020 | 0.042 | 1.000 | 2726 | tags=50%, list=15%, signal=59% | |
176 | REACTOME_RESOLUTION_OF_AP_SITES_VIA_THE_MULTIPLE_NUCLEOTIDE_PATCH_REPLACEMENT_PATHWAY | 12 | -0.68 | -1.56 | 0.027 | 0.042 | 1.000 | 1668 | tags=42%, list=9%, signal=46% | |
177 | REACTOME_ACTIVATION_OF_THE_MRNA_UPON_BINDING_OF_THE_CAP_BINDING_COMPLEX_AND_EIFS__AND_SUBSEQUENT_BINDING_TO_43S | 31 | -0.56 | -1.56 | 0.018 | 0.043 | 1.000 | 1801 | tags=29%, list=10%, signal=32% | |
178 | REACTOME_MITOCHONDRIAL_FATTY_ACID_BETA_OXIDATION | 10 | -0.72 | -1.55 | 0.044 | 0.046 | 1.000 | 2843 | tags=60%, list=15%, signal=71% | |
179 | REACTOME_ELONGATION_ARREST_AND_RECOVERY | 20 | -0.62 | -1.55 | 0.037 | 0.046 | 1.000 | 2122 | tags=50%, list=11%, signal=56% | |
180 | BIOCARTA_EUKARYOTIC PROTEIN TRANSLATION | 10 | -0.70 | -1.55 | 0.044 | 0.049 | 1.000 | 4707 | tags=90%, list=25%, signal=120% | |
181 | REACTOME_LEADING_STRAND_SYNTHESIS | 11 | -0.70 | -1.54 | 0.035 | 0.050 | 1.000 | 1404 | tags=45%, list=8%, signal=49% | |
182 | REACTOME_PAUSING_AND_RECOVERY_OF_HIV_1_ELONGATION | 20 | -0.62 | -1.54 | 0.029 | 0.050 | 1.000 | 2122 | tags=50%, list=11%, signal=56% | |
183 | HUMANCYC_DE NOVO BIOSYNTHESIS OF PYRIMIDINE DEOXYRIBONUCLEOTIDES | 11 | -0.70 | -1.54 | 0.035 | 0.050 | 1.000 | 1572 | tags=55%, list=8%, signal=60% | |
184 | HUMANCYC_GLYCOLYSIS V | 18 | -0.62 | -1.54 | 0.042 | 0.051 | 1.000 | 1193 | tags=33%, list=6%, signal=36% | |
185 | REACTOME_POLYMERASE_SWITCHING_ON_THE_C_STRAND_OF_THE_TELOMERE | 11 | -0.70 | -1.53 | 0.032 | 0.053 | 1.000 | 1404 | tags=45%, list=8%, signal=49% | |
186 | BIOCARTA_PROTEASOME COMPLEX | 22 | -0.59 | -1.53 | 0.027 | 0.054 | 1.000 | 4504 | tags=64%, list=24%, signal=84% | |
187 | REACTOME_E2F_TRANSCRIPTIONAL_TARGETS_AT_G1_S | 14 | -0.65 | -1.53 | 0.041 | 0.054 | 1.000 | 2288 | tags=50%, list=12%, signal=57% | |
188 | REACTOME_RNA_POLYMERASE_I_TRANSCRIPTION | 19 | -0.60 | -1.52 | 0.048 | 0.057 | 1.000 | 2726 | tags=47%, list=15%, signal=55% | |
189 | REACTOME_METABOLISM_OF_CARBOHYDRATES | 70 | -0.47 | -1.52 | 0.015 | 0.057 | 1.000 | 3380 | tags=39%, list=18%, signal=47% | |
190 | NCI_FOXM1 TRANSCRIPTION FACTOR NETWORK | 34 | -0.53 | -1.52 | 0.026 | 0.057 | 1.000 | 1423 | tags=18%, list=8%, signal=19% | |
191 | REACTOME_RNA_POLYMERASE_III_TRANSCRIPTION_INITIATION_FROM_TYPE_3_PROMOTER | 10 | -0.69 | -1.51 | 0.052 | 0.061 | 1.000 | 2135 | tags=50%, list=11%, signal=56% | |
192 | BIOCARTA_CELL CYCLE: G1/S CHECK POINT | 25 | -0.57 | -1.51 | 0.042 | 0.061 | 1.000 | 963 | tags=28%, list=5%, signal=29% | |
193 | REACTOME_L13A_MEDIATED_TRANSLATIONAL_SILENCING_OF_CERULOPLASMIN_EXPRESSION | 52 | -0.48 | -1.51 | 0.028 | 0.062 | 1.000 | 2256 | tags=27%, list=12%, signal=31% | |
194 | REACTOME__3___UTR_MEDIATED_TRANSLATIONAL_REGULATION | 52 | -0.48 | -1.50 | 0.021 | 0.065 | 1.000 | 2256 | tags=27%, list=12%, signal=31% | |
195 | REACTOME_RIBOSOMAL_SCANNING_AND_START_CODON_RECOGNITION | 30 | -0.53 | -1.48 | 0.050 | 0.072 | 1.000 | 1801 | tags=27%, list=10%, signal=29% | |
196 | REACTOME_PURINE_METABOLISM | 39 | -0.50 | -1.47 | 0.028 | 0.078 | 1.000 | 860 | tags=31%, list=5%, signal=32% | |
197 | BIOCARTA_CYCLINS AND CELL CYCLE REGULATION | 22 | -0.57 | -1.47 | 0.033 | 0.079 | 1.000 | 2299 | tags=45%, list=12%, signal=52% | |
198 | REACTOME_RNA_POLYMERASE_III_TRANSCRIPTION_INITIATION | 11 | -0.65 | -1.46 | 0.083 | 0.083 | 1.000 | 2135 | tags=45%, list=11%, signal=51% | |
199 | REACTOME_GTP_HYDROLYSIS_AND_JOINING_OF_THE_60S_RIBOSOMAL_SUBUNIT | 53 | -0.47 | -1.46 | 0.024 | 0.087 | 1.000 | 2256 | tags=26%, list=12%, signal=30% | |
200 | REACTOME_DUAL_INCISION_REACTION_IN_GG_NER | 17 | -0.59 | -1.45 | 0.063 | 0.090 | 1.000 | 2458 | tags=47%, list=13%, signal=54% | |
201 | REACTOME_TRANSLATION_INITIATION_COMPLEX_FORMATION | 30 | -0.53 | -1.44 | 0.047 | 0.093 | 1.000 | 1801 | tags=27%, list=10%, signal=29% | |
202 | HUMANCYC_SALVAGE PATHWAYS OF PURINE AND PYRIMIDINE NUCLEOTIDES | 19 | -0.57 | -1.44 | 0.064 | 0.094 | 1.000 | 1338 | tags=32%, list=7%, signal=34% | |
203 | HUMANCYC_GLYCOLYSIS I | 20 | -0.56 | -1.44 | 0.061 | 0.094 | 1.000 | 1193 | tags=30%, list=6%, signal=32% | |
204 | HUMANCYC_GLYCOLYSIS III | 21 | -0.56 | -1.42 | 0.056 | 0.106 | 1.000 | 1193 | tags=29%, list=6%, signal=30% | |
205 | HUMANCYC_COLANIC ACID BUILDING BLOCKS BIOSYNTHESIS | 10 | -0.66 | -1.42 | 0.080 | 0.105 | 1.000 | 1592 | tags=40%, list=9%, signal=44% | |
206 | REACTOME_LOSS_OF_PROTEINS_REQUIRED_FOR_INTERPHASE_MICROTUBULE_ORGANIZATION_FROM_THE_CENTROSOME | 31 | -0.50 | -1.42 | 0.063 | 0.108 | 1.000 | 3377 | tags=45%, list=18%, signal=55% | |
207 | HUMANCYC_SUPERPATHWAY OF GLYCOLYSIS, PYRUVATE DEHYDROGENASE, TCA, AND GLYOXYLATE BYPASS | 39 | -0.48 | -1.42 | 0.050 | 0.108 | 1.000 | 2952 | tags=38%, list=16%, signal=46% | |
208 | REACTOME_FORMATION_OF_INCISION_COMPLEX_IN_GG_NER | 17 | -0.59 | -1.41 | 0.084 | 0.112 | 1.000 | 2458 | tags=47%, list=13%, signal=54% | |
209 | BIOCARTA_ROLE OF RAN IN MITOTIC SPINDLE REGULATION | 11 | -0.64 | -1.41 | 0.075 | 0.112 | 1.000 | 3836 | tags=73%, list=21%, signal=92% | |
210 | HUMANCYC_SUPERPATHWAY OF GLYOXYLATE CYCLE | 10 | -0.65 | -1.40 | 0.110 | 0.118 | 1.000 | 5030 | tags=80%, list=27%, signal=110% | |
211 | BIOCARTA_MECHANISM OF PROTEIN IMPORT INTO THE NUCLEUS | 11 | -0.64 | -1.39 | 0.085 | 0.123 | 1.000 | 3267 | tags=73%, list=18%, signal=88% | |
212 | HUMANCYC_PURINE NUCLEOTIDES DE NOVO BIOSYNTHESIS II | 10 | -0.64 | -1.39 | 0.123 | 0.129 | 1.000 | 479 | tags=60%, list=3%, signal=62% | |
213 | HUMANCYC_SUPERPATHWAY OF GLYCOLYSIS AND ENTNER-DOUDOROFF | 22 | -0.54 | -1.38 | 0.082 | 0.129 | 1.000 | 1193 | tags=27%, list=6%, signal=29% | |
214 | REACTOME_AMINO_ACID_AND_OLIGOPEPTIDE_SLC_TRANSPORTERS | 18 | -0.55 | -1.38 | 0.103 | 0.130 | 1.000 | 7286 | tags=72%, list=39%, signal=119% | |
215 | REACTOME_AMINO_ACID_TRANSPORT_ACROSS_THE_PLASMA_MEMBRANE | 12 | -0.60 | -1.38 | 0.115 | 0.135 | 1.000 | 6174 | tags=67%, list=33%, signal=100% | |
216 | BIOCARTA_REGULATION OF P27 PHOSPHORYLATION DURING CELL CYCLE PROGRESSION | 11 | -0.63 | -1.37 | 0.109 | 0.137 | 1.000 | 4633 | tags=82%, list=25%, signal=109% | |
217 | REACTOME_PURINE_BIOSYNTHESIS | 24 | -0.50 | -1.37 | 0.121 | 0.141 | 1.000 | 3504 | tags=63%, list=19%, signal=77% | |
218 | BIOCARTA_ROLE OF MITOCHONDRIA IN APOPTOTIC SIGNALING | 12 | -0.61 | -1.36 | 0.109 | 0.145 | 1.000 | 2875 | tags=58%, list=15%, signal=69% | |
219 | BIOCARTA_SKELETAL MUSCLE HYPERTROPHY IS REGULATED VIA AKT-MTOR PATHWAY | 24 | -0.51 | -1.35 | 0.095 | 0.152 | 1.000 | 2020 | tags=38%, list=11%, signal=42% | |
220 | REACTOME_CENTROSOME_MATURATION | 33 | -0.46 | -1.31 | 0.122 | 0.190 | 1.000 | 3377 | tags=42%, list=18%, signal=52% | |
221 | REACTOME_INSULIN_SYNTHESIS_AND_SECRETION | 66 | -0.40 | -1.31 | 0.073 | 0.191 | 1.000 | 3974 | tags=30%, list=21%, signal=38% | |
222 | REACTOME_RECRUITMENT_OF_MITOTIC_CENTROSOME_PROTEINS_AND_COMPLEXES | 33 | -0.46 | -1.31 | 0.084 | 0.192 | 1.000 | 3377 | tags=42%, list=18%, signal=52% | |
223 | REACTOME_VIRAL_MRNA_TRANSLATION | 46 | -0.43 | -1.31 | 0.099 | 0.191 | 1.000 | 2256 | tags=22%, list=12%, signal=25% | |
224 | REACTOME_G2_M_TRANSITION | 44 | -0.43 | -1.31 | 0.102 | 0.192 | 1.000 | 3377 | tags=36%, list=18%, signal=44% | |
225 | INOH_CYTOKINE RECEPTOR DEGRADATION SIGNALING | 20 | -0.50 | -1.29 | 0.133 | 0.206 | 1.000 | 4504 | tags=60%, list=24%, signal=79% | |
226 | NCI_CIRCADIAN RHYTHM PATHWAY | 11 | -0.58 | -1.28 | 0.181 | 0.218 | 1.000 | 2681 | tags=55%, list=14%, signal=64% | |
227 | REACTOME_EUKARYOTIC_TRANSLATION_ELONGATION | 47 | -0.42 | -1.28 | 0.118 | 0.223 | 1.000 | 2256 | tags=23%, list=12%, signal=27% | |
228 | BIOCARTA_GRANZYME A MEDIATED APOPTOSIS PATHWAY | 12 | -0.57 | -1.27 | 0.178 | 0.226 | 1.000 | 3187 | tags=33%, list=17%, signal=40% | |
229 | BIOCARTA_CCR3 SIGNALING IN EOSINOPHILS | 21 | -0.49 | -1.27 | 0.163 | 0.229 | 1.000 | 1845 | tags=19%, list=10%, signal=21% | |
230 | REACTOME_REMOVAL_OF_THE_FLAP_INTERMEDIATE | 11 | -0.57 | -1.26 | 0.217 | 0.242 | 1.000 | 1847 | tags=36%, list=10%, signal=40% | |
231 | BIOCARTA_HEMOGLOBINS CHAPERONE | 10 | -0.58 | -1.25 | 0.215 | 0.250 | 1.000 | 4184 | tags=60%, list=22%, signal=77% | |
232 | REACTOME_APOPTOSIS | 94 | -0.37 | -1.25 | 0.112 | 0.254 | 1.000 | 3325 | tags=39%, list=18%, signal=48% | |
233 | REACTOME_PROCESSIVE_SYNTHESIS_ON_THE_LAGGING_STRAND | 12 | -0.54 | -1.24 | 0.201 | 0.267 | 1.000 | 1847 | tags=33%, list=10%, signal=37% | |
234 | REACTOME_GLUCONEOGENESIS | 11 | -0.56 | -1.23 | 0.217 | 0.270 | 1.000 | 2903 | tags=55%, list=16%, signal=65% | |
235 | REACTOME_HOMOLOGOUS_RECOMBINATION_REPAIR_OF_REPLICATION_INDEPENDENT_DOUBLE_STRAND_BREAKS | 12 | -0.54 | -1.23 | 0.227 | 0.276 | 1.000 | 3463 | tags=50%, list=19%, signal=61% | |
236 | REACTOME_HOMOLOGOUS_RECOMBINATION_REPAIR | 12 | -0.54 | -1.22 | 0.220 | 0.285 | 1.000 | 3463 | tags=50%, list=19%, signal=61% | |
237 | REACTOME_EUKARYOTIC_TRANSLATION_TERMINATION | 46 | -0.40 | -1.22 | 0.167 | 0.289 | 1.000 | 2256 | tags=22%, list=12%, signal=25% | |
238 | BIOCARTA_REGULATION OF EIF2 | 10 | -0.56 | -1.21 | 0.258 | 0.302 | 1.000 | 1705 | tags=40%, list=9%, signal=44% | |
239 | BIOCARTA_REGULATION OF CELL CYCLE PROGRESSION BY PLK3 | 17 | -0.48 | -1.20 | 0.209 | 0.308 | 1.000 | 3051 | tags=59%, list=16%, signal=70% | |
240 | BIOCARTA_PTEN DEPENDENT CELL CYCLE ARREST AND APOPTOSIS | 15 | -0.50 | -1.20 | 0.245 | 0.311 | 1.000 | 9 | tags=7%, list=0%, signal=7% | |
241 | REACTOME_PEPTIDE_CHAIN_ELONGATION | 45 | -0.39 | -1.19 | 0.190 | 0.313 | 1.000 | 2256 | tags=22%, list=12%, signal=25% | |
242 | REACTOME_TRANSMEMBRANE_TRANSPORT_OF_SMALL_MOLECULES | 64 | -0.37 | -1.19 | 0.176 | 0.323 | 1.000 | 3829 | tags=34%, list=21%, signal=43% | |
243 | CELLMAP_TNF ALPHA/NF-KB | 155 | -0.32 | -1.18 | 0.138 | 0.328 | 1.000 | 2925 | tags=30%, list=16%, signal=35% | |
244 | REACTOME_SLC_MEDIATED_TRANSMEMBRANE_TRANSPORT | 57 | -0.37 | -1.18 | 0.189 | 0.330 | 1.000 | 3829 | tags=33%, list=21%, signal=42% | |
245 | REACTOME_MITOTIC_PROMETAPHASE | 38 | -0.40 | -1.17 | 0.232 | 0.336 | 1.000 | 3844 | tags=32%, list=21%, signal=40% | |
246 | BIOCARTA_LISSENCEPHALY GENE (LIS1) IN NEURONAL MIGRATION AND DEVELOPMENT | 15 | -0.48 | -1.17 | 0.272 | 0.345 | 1.000 | 628 | tags=20%, list=3%, signal=21% | |
247 | NCI_ARF6 DOWNSTREAM PATHWAY | 25 | -0.43 | -1.16 | 0.246 | 0.349 | 1.000 | 773 | tags=16%, list=4%, signal=17% | |
248 | BIOCARTA_UCALPAIN AND FRIENDS IN CELL SPREAD | 13 | -0.50 | -1.16 | 0.298 | 0.355 | 1.000 | 9 | tags=8%, list=0%, signal=8% | |
249 | HUMANCYC_TCA CYCLE | 16 | -0.47 | -1.16 | 0.268 | 0.354 | 1.000 | 4423 | tags=63%, list=24%, signal=82% | |
250 | HUMANCYC_RESPIRATION (ANAEROBIC) | 16 | -0.49 | -1.16 | 0.277 | 0.356 | 1.000 | 2952 | tags=44%, list=16%, signal=52% | |
251 | REACTOME_M_PHASE | 40 | -0.38 | -1.15 | 0.248 | 0.364 | 1.000 | 2586 | tags=23%, list=14%, signal=26% | |
252 | REACTOME_INTRINSIC_PATHWAY_FOR_APOPTOSIS | 22 | -0.44 | -1.15 | 0.252 | 0.369 | 1.000 | 2897 | tags=45%, list=16%, signal=54% | |
253 | HUMANCYC_SUPERPATHWAY OF GLYOXYLATE BYPASS AND TCA | 16 | -0.47 | -1.15 | 0.291 | 0.368 | 1.000 | 4423 | tags=63%, list=24%, signal=82% | |
254 | NCI_HYPOXIC AND OXYGEN HOMEOSTASIS REGULATION OF HIF-1-ALPHA | 67 | -0.35 | -1.14 | 0.214 | 0.369 | 1.000 | 1193 | tags=12%, list=6%, signal=13% | |
255 | BIOCARTA_CELL TO CELL ADHESION SIGNALING | 10 | -0.53 | -1.13 | 0.297 | 0.396 | 1.000 | 9 | tags=10%, list=0%, signal=10% | |
256 | NCI_ARF1 PATHWAY | 13 | -0.49 | -1.12 | 0.319 | 0.405 | 1.000 | 773 | tags=15%, list=4%, signal=16% | |
257 | HUMANCYC_FATTY ACID BETA-OXIDATION I | 16 | -0.46 | -1.12 | 0.316 | 0.404 | 1.000 | 1555 | tags=25%, list=8%, signal=27% | |
258 | REACTOME_FORMATION_OF_A_POOL_OF_FREE_40S_SUBUNITS | 44 | -0.37 | -1.12 | 0.262 | 0.406 | 1.000 | 2256 | tags=20%, list=12%, signal=23% | |
259 | HUMANCYC_GLUCONEOGENESIS | 17 | -0.46 | -1.11 | 0.338 | 0.409 | 1.000 | 2903 | tags=41%, list=16%, signal=49% | |
260 | BIOCARTA_CARDIAC PROTECTION AGAINST ROS | 11 | -0.50 | -1.11 | 0.334 | 0.408 | 1.000 | 378 | tags=9%, list=2%, signal=9% | |
261 | BIOCARTA_ROLE OF NICOTINIC ACETYLCHOLINE RECEPTORS IN THE REGULATION OF APOPTOSIS | 17 | -0.45 | -1.11 | 0.314 | 0.409 | 1.000 | 9 | tags=6%, list=0%, signal=6% | |
262 | REACTOME_ACTIVATION_OF_BH3_ONLY_PROTEINS | 11 | -0.49 | -1.11 | 0.349 | 0.418 | 1.000 | 2897 | tags=55%, list=16%, signal=65% | |
263 | NCI_NONGENOTROPIC ANDROGEN SIGNALING | 24 | -0.40 | -1.09 | 0.331 | 0.447 | 1.000 | 9 | tags=4%, list=0%, signal=4% | |
264 | REACTOME_SPHINGOLIPID_METABOLISM | 10 | -0.49 | -1.07 | 0.375 | 0.471 | 1.000 | 2423 | tags=40%, list=13%, signal=46% | |
265 | BIOCARTA_CHROMATIN REMODELING BY HSWI/SNF ATP-DEPENDENT COMPLEXES | 15 | -0.45 | -1.07 | 0.388 | 0.473 | 1.000 | 2798 | tags=40%, list=15%, signal=47% | |
266 | INOH_RAP1 ACTIVATION SIGNALING (THROUGH CAMP AND EPAC) | 22 | -0.41 | -1.06 | 0.359 | 0.486 | 1.000 | 620 | tags=9%, list=3%, signal=9% | |
267 | BIOCARTA_REGULATION OF EIF-4E AND P70S6 KINASE | 22 | -0.41 | -1.06 | 0.365 | 0.494 | 1.000 | 2020 | tags=32%, list=11%, signal=36% | |
268 | BIOCARTA_MTOR SIGNALING PATHWAY | 22 | -0.40 | -1.05 | 0.390 | 0.505 | 1.000 | 5577 | tags=55%, list=30%, signal=78% | |
269 | INOH_B-RAF ACTIVATION SIGNALING | 26 | -0.39 | -1.05 | 0.375 | 0.505 | 1.000 | 620 | tags=8%, list=3%, signal=8% | |
270 | BIOCARTA_CONTROL OF GENE EXPRESSION BY VITAMIN D RECEPTOR | 22 | -0.40 | -1.04 | 0.392 | 0.521 | 1.000 | 1599 | tags=23%, list=9%, signal=25% | |
271 | REACTOME_SYNTHESIS_OF_GPI_ANCHORED_PROTEINS | 11 | -0.46 | -1.04 | 0.438 | 0.528 | 1.000 | 4603 | tags=45%, list=25%, signal=60% | |
272 | INOH_TGF BETA RECEPTOR I DEGRADATION SIGNALING | 25 | -0.39 | -1.04 | 0.419 | 0.526 | 1.000 | 2983 | tags=36%, list=16%, signal=43% | |
273 | BIOCARTA_PHOSPHOINOSITIDES AND THEIR DOWNSTREAM TARGETS | 21 | -0.40 | -1.03 | 0.410 | 0.526 | 1.000 | 2020 | tags=19%, list=11%, signal=21% | |
274 | BIOCARTA_P53 SIGNALING PATHWAY | 13 | -0.45 | -1.03 | 0.431 | 0.524 | 1.000 | 2875 | tags=54%, list=15%, signal=64% | |
275 | REACTOME_AMINE_LIGAND_BINDING_RECEPTORS | 12 | -0.45 | -1.03 | 0.418 | 0.525 | 1.000 | 7557 | tags=58%, list=41%, signal=98% | |
276 | REACTOME_PI3K_CASCADE | 12 | -0.46 | -1.03 | 0.438 | 0.534 | 1.000 | 2950 | tags=58%, list=16%, signal=69% | |
277 | INOH_TGF BETA RECEPTOR COMPLEX DEGRADATION SIGNALING | 29 | -0.36 | -1.03 | 0.417 | 0.533 | 1.000 | 2983 | tags=31%, list=16%, signal=37% | |
278 | NCI_SUMOYLATION BY RANBP2 REGULATES TRANSCRIPTIONAL REPRESSION | 10 | -0.47 | -1.02 | 0.438 | 0.541 | 1.000 | 3267 | tags=60%, list=18%, signal=73% | |
279 | REACTOME_METABOLISM_OF_LIPIDS_AND_LIPOPROTEINS | 110 | -0.29 | -1.02 | 0.407 | 0.547 | 1.000 | 3003 | tags=23%, list=16%, signal=27% | |
280 | BIOCARTA_INFLUENCE OF RAS AND RHO PROTEINS ON G1 TO S TRANSITION | 28 | -0.37 | -1.01 | 0.453 | 0.564 | 1.000 | 2299 | tags=29%, list=12%, signal=33% | |
281 | HUMANCYC_ISOLEUCINE DEGRADATION III | 13 | -0.43 | -1.00 | 0.465 | 0.581 | 1.000 | 3336 | tags=46%, list=18%, signal=56% | |
282 | HUMANCYC_ENTNER-DOUDOROFF PATHWAY II (NON-PHOSPHORYLATIVE) | 12 | -0.43 | -0.99 | 0.469 | 0.600 | 1.000 | 1193 | tags=25%, list=6%, signal=27% | |
283 | BIOCARTA_CTCF: FIRST MULTIVALENT NUCLEAR FACTOR | 23 | -0.37 | -0.99 | 0.492 | 0.599 | 1.000 | 2 | tags=4%, list=0%, signal=4% | |
284 | BIOCARTA_IL-2 RECEPTOR BETA CHAIN IN T CELL ACTIVATION | 48 | -0.32 | -0.98 | 0.487 | 0.607 | 1.000 | 2288 | tags=23%, list=12%, signal=26% | |
285 | HUMANCYC_FATTY ACID BETA-OXIDATION II (CORE PATHWAY) | 16 | -0.40 | -0.98 | 0.479 | 0.609 | 1.000 | 4070 | tags=38%, list=22%, signal=48% | |
286 | INOH_SNON DEGRADATION SIGNALING | 25 | -0.37 | -0.98 | 0.509 | 0.609 | 1.000 | 2983 | tags=40%, list=16%, signal=48% | |
287 | NCI_LISSENCEPHALY GENE (LIS1) IN NEURONAL MIGRATION AND DEVELOPMENT | 26 | -0.36 | -0.98 | 0.481 | 0.608 | 1.000 | 530 | tags=12%, list=3%, signal=12% | |
288 | BIOCARTA_ENDOCYTOTIC ROLE OF NDK PHOSPHINS AND DYNAMIN | 14 | -0.42 | -0.97 | 0.508 | 0.615 | 1.000 | 159 | tags=14%, list=1%, signal=14% | |
289 | NCI_SYNDECAN-4-MEDIATED SIGNALING EVENTS | 47 | -0.32 | -0.97 | 0.495 | 0.615 | 1.000 | 208 | tags=4%, list=1%, signal=4% | |
290 | NCI_MTOR SIGNALING PATHWAY | 24 | -0.36 | -0.97 | 0.494 | 0.620 | 1.000 | 5577 | tags=58%, list=30%, signal=83% | |
291 | BIOCARTA_VEGF HYPOXIA AND ANGIOGENESIS | 28 | -0.35 | -0.96 | 0.497 | 0.623 | 1.000 | 9 | tags=4%, list=0%, signal=4% | |
292 | BIOCARTA_CHREBP REGULATION BY CARBOHYDRATES AND CAMP | 34 | -0.33 | -0.96 | 0.521 | 0.627 | 1.000 | 1645 | tags=15%, list=9%, signal=16% | |
293 | BIOCARTA_ATM SIGNALING PATHWAY | 16 | -0.40 | -0.95 | 0.527 | 0.644 | 1.000 | 2897 | tags=44%, list=16%, signal=52% | |
294 | REACTOME_CHEMOKINE_RECEPTORS_BIND_CHEMOKINES | 13 | -0.41 | -0.95 | 0.528 | 0.651 | 1.000 | 195 | tags=8%, list=1%, signal=8% | |
295 | REACTOME_MEMBRANE_TRAFFICKING | 26 | -0.35 | -0.95 | 0.506 | 0.649 | 1.000 | 1654 | tags=19%, list=9%, signal=21% | |
296 | REACTOME_GOLGI_ASSOCIATED_VESICLE_BIOGENESIS | 12 | -0.43 | -0.95 | 0.557 | 0.651 | 1.000 | 435 | tags=17%, list=2%, signal=17% | |
297 | BIOCARTA_REGULATION OF CK1/CDK5 BY TYPE 1 GLUTAMATE RECEPTORS | 22 | -0.36 | -0.94 | 0.527 | 0.650 | 1.000 | 1645 | tags=23%, list=9%, signal=25% | |
298 | REACTOME_INTEGRIN_ALPHAIIBBETA3_SIGNALING | 17 | -0.38 | -0.94 | 0.553 | 0.659 | 1.000 | 1210 | tags=12%, list=6%, signal=13% | |
299 | NCI_PAXILLIN-INDEPENDENT EVENTS MEDIATED BY A4B1 AND A4B7 | 21 | -0.36 | -0.93 | 0.547 | 0.679 | 1.000 | 9 | tags=5%, list=0%, signal=5% | |
300 | REACTOME_PLATELET_AGGREGATION__PLUG_FORMATION_ | 18 | -0.37 | -0.93 | 0.544 | 0.678 | 1.000 | 1210 | tags=11%, list=6%, signal=12% | |
301 | NCI_E-CADHERIN SIGNALING IN THE NASCENT ADHERENS JUNCTION | 37 | -0.32 | -0.92 | 0.595 | 0.691 | 1.000 | 159 | tags=8%, list=1%, signal=8% | |
302 | BIOCARTA_ATTENUATION OF GPCR SIGNALING | 11 | -0.42 | -0.91 | 0.575 | 0.707 | 1.000 | 1645 | tags=27%, list=9%, signal=30% | |
303 | REACTOME_TRANS_GOLGI_NETWORK_VESICLE_BUDDING | 15 | -0.37 | -0.91 | 0.600 | 0.705 | 1.000 | 435 | tags=13%, list=2%, signal=14% | |
304 | BIOCARTA_THE INFORMATION PROCESSING PATHWAY AT THE IFN BETA ENHANCER | 26 | -0.34 | -0.90 | 0.605 | 0.719 | 1.000 | 2845 | tags=31%, list=15%, signal=36% | |
305 | REACTOME_RNA_POLYMERASE_III_TRANSCRIPTION | 16 | -0.37 | -0.90 | 0.604 | 0.717 | 1.000 | 2135 | tags=31%, list=11%, signal=35% | |
306 | BIOCARTA_PHOSPHOLIPASE C-EPSILON PATHWAY | 11 | -0.41 | -0.90 | 0.615 | 0.716 | 1.000 | 1645 | tags=27%, list=9%, signal=30% | |
307 | INOH_ADENYLATE CYCLASE ACTIVATION SIGNALING | 11 | -0.40 | -0.90 | 0.603 | 0.714 | 1.000 | 3832 | tags=45%, list=21%, signal=57% | |
308 | HUMANCYC_CHOLESTEROL BIOSYNTHESIS III (VIA DESMOSTEROL) | 12 | -0.40 | -0.90 | 0.623 | 0.722 | 1.000 | 1737 | tags=25%, list=9%, signal=28% | |
309 | HUMANCYC_CHOLESTEROL BIOSYNTHESIS I | 12 | -0.40 | -0.89 | 0.614 | 0.730 | 1.000 | 1737 | tags=25%, list=9%, signal=28% | |
310 | HUMANCYC_CHOLESTEROL BIOSYNTHESIS II (VIA 24,25-DIHYDROLANOSTEROL) | 12 | -0.40 | -0.89 | 0.615 | 0.734 | 1.000 | 1737 | tags=25%, list=9%, signal=28% | |
311 | REACTOME_IRS_MEDIATED_SIGNALLING | 20 | -0.34 | -0.88 | 0.627 | 0.739 | 1.000 | 2950 | tags=40%, list=16%, signal=47% | |
312 | REACTOME_CLATHRIN_DERIVED_VESICLE_BUDDING | 15 | -0.37 | -0.88 | 0.642 | 0.750 | 1.000 | 435 | tags=13%, list=2%, signal=14% | |
313 | BIOCARTA_APOPTOTIC SIGNALING IN RESPONSE TO DNA DAMAGE | 14 | -0.37 | -0.88 | 0.627 | 0.749 | 1.000 | 2875 | tags=43%, list=15%, signal=51% | |
314 | REACTOME_CHYLOMICRON_MEDIATED_LIPID_TRANSPORT | 14 | -0.37 | -0.87 | 0.618 | 0.749 | 1.000 | 4887 | tags=36%, list=26%, signal=48% | |
315 | NCI_PRESENILIN ACTION IN NOTCH AND WNT SIGNALING | 40 | -0.29 | -0.86 | 0.659 | 0.763 | 1.000 | 2514 | tags=18%, list=14%, signal=20% | |
316 | BIOCARTA_NUCLEAR RECEPTORS COORDINATE THE ACTIVITIES OF CHROMATIN REMODELING COMPLEXES AND COACTIVATORS TO FACILITATE INITIATION OF TRANSCRIPTION IN CARCINOMA CELLS | 14 | -0.37 | -0.86 | 0.657 | 0.761 | 1.000 | 2798 | tags=29%, list=15%, signal=34% | |
317 | BIOCARTA_PHOSPHOLIPIDS AS SIGNALLING INTERMEDIARIES | 29 | -0.31 | -0.85 | 0.694 | 0.777 | 1.000 | 9 | tags=3%, list=0%, signal=3% | |
318 | BIOCARTA_RB TUMOR SUPPRESSOR/CHECKPOINT SIGNALING IN RESPONSE TO DNA DAMAGE | 12 | -0.38 | -0.85 | 0.662 | 0.784 | 1.000 | 3051 | tags=50%, list=16%, signal=60% | |
319 | REACTOME_INSULIN_RECEPTOR_SIGNALLING_CASCADE | 22 | -0.32 | -0.85 | 0.709 | 0.784 | 1.000 | 2950 | tags=36%, list=16%, signal=43% | |
320 | REACTOME_IRS_RELATED_EVENTS | 21 | -0.33 | -0.85 | 0.691 | 0.787 | 1.000 | 2950 | tags=38%, list=16%, signal=45% | |
321 | REACTOME_SIGNALING_BY_INSULIN_RECEPTOR | 22 | -0.32 | -0.84 | 0.691 | 0.789 | 1.000 | 2950 | tags=36%, list=16%, signal=43% | |
322 | BIOCARTA_HYPOXIA-INDUCIBLE FACTOR IN THE CARDIVASCULAR SYSTEM | 14 | -0.35 | -0.83 | 0.680 | 0.800 | 1.000 | 1706 | tags=21%, list=9%, signal=24% | |
323 | BIOCARTA_CARM1 AND REGULATION OF THE ESTROGEN RECEPTOR | 11 | -0.37 | -0.83 | 0.696 | 0.801 | 1.000 | 2798 | tags=55%, list=15%, signal=64% | |
324 | INOH_JAK DEGRADATION SIGNALING | 24 | -0.31 | -0.83 | 0.764 | 0.805 | 1.000 | 2983 | tags=42%, list=16%, signal=50% | |
325 | NCI_A4B1 AND A4B7 INTEGRIN SIGNALING | 25 | -0.30 | -0.82 | 0.752 | 0.822 | 1.000 | 9 | tags=4%, list=0%, signal=4% | |
326 | NCI_ALPHA-SYNUCLEIN SIGNALING | 32 | -0.29 | -0.81 | 0.769 | 0.830 | 1.000 | 2752 | tags=19%, list=15%, signal=22% | |
327 | NCI_FOXA2 AND FOXA3 TRANSCRIPTION FACTOR NETWORKS | 37 | -0.27 | -0.80 | 0.801 | 0.850 | 1.000 | 1747 | tags=14%, list=9%, signal=15% | |
328 | NCI_NONCANONICAL WNT SIGNALING PATHWAY | 18 | -0.31 | -0.79 | 0.767 | 0.864 | 1.000 | 208 | tags=6%, list=1%, signal=6% | |
329 | NCI_INSULIN-MEDIATED GLUCOSE TRANSPORT | 24 | -0.29 | -0.77 | 0.806 | 0.877 | 1.000 | 5218 | tags=42%, list=28%, signal=58% | |
330 | REACTOME_DOUBLE_STRAND_BREAK_REPAIR | 17 | -0.31 | -0.77 | 0.762 | 0.875 | 1.000 | 2583 | tags=29%, list=14%, signal=34% | |
331 | BIOCARTA_HOW PROGESTERONE INITIATES THE OOCYTE MATURATION | 19 | -0.31 | -0.77 | 0.763 | 0.878 | 1.000 | 1845 | tags=21%, list=10%, signal=23% | |
332 | REACTOME_AMINE_COMPOUND_SLC_TRANSPORTERS | 10 | -0.36 | -0.77 | 0.744 | 0.881 | 1.000 | 4670 | tags=30%, list=25%, signal=40% | |
333 | REACTOME_REGULATION_OF_INSULIN_SECRETION_BY_GLUCAGON_LIKE_PEPTIDE_1 | 11 | -0.34 | -0.77 | 0.762 | 0.879 | 1.000 | 4558 | tags=45%, list=24%, signal=60% | |
334 | BIOCARTA_ER ASSOCIATED DEGRADATION (ERAD) PATHWAY | 15 | -0.32 | -0.76 | 0.805 | 0.888 | 1.000 | 4633 | tags=53%, list=25%, signal=71% | |
335 | HUMANCYC_SUPERPATHWAY OF CHOLESTEROL BIOSYNTHESIS | 23 | -0.29 | -0.75 | 0.834 | 0.888 | 1.000 | 1737 | tags=17%, list=9%, signal=19% | |
336 | REACTOME_CYCLIN_A_B1_ASSOCIATED_EVENTS_DURING_G2_M_TRANSITION | 11 | -0.33 | -0.74 | 0.801 | 0.899 | 1.000 | 2140 | tags=18%, list=11%, signal=21% | |
337 | REACTOME_LIPOPROTEIN_METABOLISM | 18 | -0.30 | -0.73 | 0.859 | 0.908 | 1.000 | 4887 | tags=28%, list=26%, signal=38% | |
338 | BIOCARTA_TRANSCRIPTION REGULATION BY METHYLTRANSFERASE OF CARM1 | 12 | -0.33 | -0.73 | 0.835 | 0.909 | 1.000 | 1645 | tags=25%, list=9%, signal=27% | |
339 | BIOCARTA_STATHMIN AND BREAST CANCER RESISTANCE TO ANTIMICROTUBULE AGENTS | 19 | -0.29 | -0.72 | 0.857 | 0.913 | 1.000 | 1645 | tags=16%, list=9%, signal=17% | |
340 | REACTOME_INORGANIC_CATION_ANION_SLC_TRANSPORTERS | 12 | -0.32 | -0.72 | 0.856 | 0.918 | 1.000 | 3409 | tags=42%, list=18%, signal=51% | |
341 | INOH_WNT SECRETORY PATHWAY (CANONICAL) | 47 | -0.23 | -0.70 | 0.942 | 0.937 | 1.000 | 5837 | tags=32%, list=31%, signal=46% | |
342 | BIOCARTA_STRESS INDUCTION OF HSP REGULATION | 14 | -0.28 | -0.67 | 0.876 | 0.955 | 1.000 | 3729 | tags=36%, list=20%, signal=45% | |
343 | BIOCARTA_IL-10 ANTI-INFLAMMATORY SIGNALING PATHWAY | 13 | -0.29 | -0.67 | 0.883 | 0.954 | 1.000 | 1320 | tags=15%, list=7%, signal=17% | |
344 | REACTOME_TRAF6_MEDIATED_INDUCTION_OF_THE_ANTIVIRAL_CYTOKINE_IFN_ALPHA_BETA_CASCADE | 12 | -0.29 | -0.64 | 0.937 | 0.967 | 1.000 | 3503 | tags=33%, list=19%, signal=41% | |
345 | HUMANCYC_SUPERPATHWAY OF CITRULLINE METABOLISM | 11 | -0.27 | -0.61 | 0.919 | 0.980 | 1.000 | 1450 | tags=9%, list=8%, signal=10% | |
346 | REACTOME_REGULATION_OF_LIPID_METABOLISM_BY_PEROXISOME_PROLIFERATOR_ACTIVATED_RECEPTOR_ALPHA__PPARALPHA_ | 11 | -0.26 | -0.57 | 0.957 | 0.995 | 1.000 | 3620 | tags=27%, list=19%, signal=34% | |
347 | INOH_WNT SECRETORY PATHWAY (MAMMAL) | 48 | -0.18 | -0.54 | 1.000 | 1.000 | 1.000 | 5837 | tags=31%, list=31%, signal=45% | |
348 | BIOCARTA_CADMIUM INDUCES DNA SYNTHESIS AND PROLIFERATION IN MACROPHAGES | 15 | -0.21 | -0.51 | 0.982 | 1.000 | 1.000 | 4925 | tags=33%, list=26%, signal=45% | |
349 | REACTOME_PEPTIDE_LIGAND_BINDING_RECEPTORS | 53 | -0.16 | -0.49 | 1.000 | 1.000 | 1.000 | 4052 | tags=17%, list=22%, signal=22% | |
350 | REACTOME_COMPLEMENT_CASCADE | 14 | -0.21 | -0.48 | 0.989 | 1.000 | 1.000 | 14770 | tags=100%, list=79%, signal=484% | |
351 | BIOCARTA_ION CHANNELS AND THEIR FUNCTIONAL ROLE IN VASCULAR ENDOTHELIUM | 41 | -0.16 | -0.47 | 1.000 | 1.000 | 1.000 | 208 | tags=2%, list=1%, signal=2% | |
352 | BIOCARTA_CLASSICAL COMPLEMENT PATHWAY | 10 | -0.21 | -0.45 | 0.985 | 0.999 | 1.000 | 14770 | tags=100%, list=79%, signal=484% | |
353 | REACTOME_SYNTHESIS_OF_BILE_ACIDS_AND_BILE_SALTS | 10 | -0.18 | -0.39 | 1.000 | 0.999 | 1.000 | 5462 | tags=40%, list=29%, signal=57% |