date generated: 2020-07-13
Mitch performs unidimensional and multidimensional gene set enrichment analysis. The concept behind this dates to work by Cox and Mann (https://doi.org/10.1186/1471-2105-13-S16-S12). This implementation is suited to R based workflows of multi-omics datasets. This software was developed by Antony Kaspi and Mark Ziemann. Learn more about Mitch at the website: https://github.com/markziemann/Mitch
Here is the first few lines of the input profile.
## x
## 5S_rRNA 3.1729765
## 7SK 4.1979466
## A1BG 0.4203060
## A1CF -0.7100788
## A2M 0.7954409
## A3GALT2 -1.2495566
Here are some metrics about the input data profile:
| Profile metrics | |
|---|---|
| num_genesets | 2400 |
| num_genes_in_profile | 16348 |
| duplicated_genes_present | 0 |
| num_profile_genes_in_sets | 8696 |
| num_profile_genes_not_in_sets | 7652 |
Here is a plot of the input profiles. Note the dynamic ranges.
Here is the contour plot of the profile including all detected genes.
Here are some metrics about the gene sets used: GMT file of genesets: ReactomePathways.gmt
| Gene sets metrics | |
|---|---|
| num_genesets | 2400 |
| num_genesets_excluded | 1009 |
| num_genesets_included | 1391 |
Significance is calculated by -log10(p-value). All points shown are FDR<0.05.
Top N= 50 gene sets
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Olfactory Signaling Pathway | 279 | 4.49e-71 | 0.619 | 6.25e-68 |
| Glucuronidation | 17 | 1.53e-04 | 0.530 | 2.33e-02 |
| Passive transport by Aquaporins | 12 | 4.60e-03 | -0.472 | 2.97e-01 |
| TRAF6 mediated IRF7 activation | 28 | 2.21e-05 | 0.463 | 3.85e-03 |
| G alpha (s) signalling events | 408 | 4.62e-50 | 0.429 | 3.21e-47 |
| Class C/3 (Metabotropic glutamate/pheromone receptors) | 34 | 1.62e-05 | 0.427 | 3.21e-03 |
| PI3K events in ERBB4 signaling | 10 | 2.04e-02 | 0.423 | 4.21e-01 |
| Removal of the Flap Intermediate | 11 | 1.60e-02 | -0.419 | 4.21e-01 |
| SHC1 events in ERBB4 signaling | 14 | 7.62e-03 | 0.412 | 3.74e-01 |
| Regulation of IFNA signaling | 25 | 4.86e-04 | 0.403 | 5.20e-02 |
| Diseases associated with glycosylation precursor biosynthesis | 16 | 5.47e-03 | -0.401 | 3.31e-01 |
| ATF6 (ATF6-alpha) activates chaperones | 10 | 2.94e-02 | 0.398 | 4.39e-01 |
| Glutathione synthesis and recycling | 12 | 1.80e-02 | -0.394 | 4.21e-01 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 12 | 1.95e-02 | 0.390 | 4.21e-01 |
| GRB2 events in ERBB2 signaling | 16 | 7.19e-03 | 0.388 | 3.74e-01 |
| CREB1 phosphorylation through the activation of Adenylate Cyclase | 11 | 2.69e-02 | 0.385 | 4.21e-01 |
| Synthesis of PA | 30 | 2.68e-04 | -0.384 | 3.39e-02 |
| Mitotic Telophase/Cytokinesis | 10 | 3.58e-02 | 0.383 | 4.69e-01 |
| Adherens junctions interactions | 24 | 1.20e-03 | 0.382 | 1.11e-01 |
| GRB2 events in EGFR signaling | 13 | 1.72e-02 | 0.382 | 4.21e-01 |
| MET activates RAP1 and RAC1 | 11 | 3.07e-02 | 0.376 | 4.50e-01 |
| Metabolism of folate and pterines | 14 | 1.54e-02 | -0.374 | 4.21e-01 |
| Dermatan sulfate biosynthesis | 11 | 3.19e-02 | 0.374 | 4.51e-01 |
| Glutamate and glutamine metabolism | 13 | 2.16e-02 | -0.368 | 4.21e-01 |
| Acyl chain remodelling of PS | 18 | 8.55e-03 | -0.358 | 3.74e-01 |
| Pre-NOTCH Processing in Golgi | 14 | 2.08e-02 | -0.357 | 4.21e-01 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 14 | 2.18e-02 | -0.354 | 4.21e-01 |
| Aflatoxin activation and detoxification | 16 | 1.44e-02 | -0.353 | 4.21e-01 |
| SHC1 events in EGFR signaling | 14 | 2.31e-02 | 0.351 | 4.21e-01 |
| Termination of O-glycan biosynthesis | 19 | 9.85e-03 | -0.342 | 4.15e-01 |
| PI3K events in ERBB2 signaling | 16 | 1.99e-02 | 0.336 | 4.21e-01 |
| Activation of RAC1 | 12 | 4.43e-02 | 0.335 | 5.01e-01 |
| Removal of the Flap Intermediate from the C-strand | 12 | 4.48e-02 | -0.335 | 5.01e-01 |
| Gluconeogenesis | 29 | 1.87e-03 | -0.334 | 1.63e-01 |
| Processive synthesis on the lagging strand | 12 | 4.69e-02 | -0.331 | 5.01e-01 |
| XBP1(S) activates chaperone genes | 42 | 3.05e-04 | -0.322 | 3.54e-02 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 16 | 2.64e-02 | 0.321 | 4.21e-01 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 16 | 2.69e-02 | 0.319 | 4.21e-01 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 16 | 2.69e-02 | 0.319 | 4.21e-01 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | 13 | 4.67e-02 | 0.319 | 5.01e-01 |
| Receptor-type tyrosine-protein phosphatases | 19 | 1.62e-02 | 0.319 | 4.21e-01 |
| Polymerase switching on the C-strand of the telomere | 21 | 1.17e-02 | -0.318 | 4.21e-01 |
| Constitutive Signaling by EGFRvIII | 15 | 3.36e-02 | 0.317 | 4.63e-01 |
| Signaling by EGFRvIII in Cancer | 15 | 3.36e-02 | 0.317 | 4.63e-01 |
| Signaling by EGFR in Cancer | 22 | 1.08e-02 | 0.314 | 4.21e-01 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 17 | 2.53e-02 | -0.313 | 4.21e-01 |
| CD209 (DC-SIGN) signaling | 19 | 1.84e-02 | 0.312 | 4.21e-01 |
| Acyl chain remodelling of PI | 14 | 4.33e-02 | -0.312 | 5.01e-01 |
| Signaling by Leptin | 10 | 8.82e-02 | -0.311 | 6.23e-01 |
| Activated NTRK2 signals through FRS2 and FRS3 | 10 | 8.91e-02 | 0.310 | 6.23e-01 |
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Olfactory Signaling Pathway | 279 | 4.49e-71 | 0.619000 | 6.25e-68 |
| Glucuronidation | 17 | 1.53e-04 | 0.530000 | 2.33e-02 |
| Passive transport by Aquaporins | 12 | 4.60e-03 | -0.472000 | 2.97e-01 |
| TRAF6 mediated IRF7 activation | 28 | 2.21e-05 | 0.463000 | 3.85e-03 |
| G alpha (s) signalling events | 408 | 4.62e-50 | 0.429000 | 3.21e-47 |
| Class C/3 (Metabotropic glutamate/pheromone receptors) | 34 | 1.62e-05 | 0.427000 | 3.21e-03 |
| PI3K events in ERBB4 signaling | 10 | 2.04e-02 | 0.423000 | 4.21e-01 |
| Removal of the Flap Intermediate | 11 | 1.60e-02 | -0.419000 | 4.21e-01 |
| SHC1 events in ERBB4 signaling | 14 | 7.62e-03 | 0.412000 | 3.74e-01 |
| Regulation of IFNA signaling | 25 | 4.86e-04 | 0.403000 | 5.20e-02 |
| Diseases associated with glycosylation precursor biosynthesis | 16 | 5.47e-03 | -0.401000 | 3.31e-01 |
| ATF6 (ATF6-alpha) activates chaperones | 10 | 2.94e-02 | 0.398000 | 4.39e-01 |
| Glutathione synthesis and recycling | 12 | 1.80e-02 | -0.394000 | 4.21e-01 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 12 | 1.95e-02 | 0.390000 | 4.21e-01 |
| GRB2 events in ERBB2 signaling | 16 | 7.19e-03 | 0.388000 | 3.74e-01 |
| CREB1 phosphorylation through the activation of Adenylate Cyclase | 11 | 2.69e-02 | 0.385000 | 4.21e-01 |
| Synthesis of PA | 30 | 2.68e-04 | -0.384000 | 3.39e-02 |
| Mitotic Telophase/Cytokinesis | 10 | 3.58e-02 | 0.383000 | 4.69e-01 |
| Adherens junctions interactions | 24 | 1.20e-03 | 0.382000 | 1.11e-01 |
| GRB2 events in EGFR signaling | 13 | 1.72e-02 | 0.382000 | 4.21e-01 |
| MET activates RAP1 and RAC1 | 11 | 3.07e-02 | 0.376000 | 4.50e-01 |
| Metabolism of folate and pterines | 14 | 1.54e-02 | -0.374000 | 4.21e-01 |
| Dermatan sulfate biosynthesis | 11 | 3.19e-02 | 0.374000 | 4.51e-01 |
| Glutamate and glutamine metabolism | 13 | 2.16e-02 | -0.368000 | 4.21e-01 |
| Acyl chain remodelling of PS | 18 | 8.55e-03 | -0.358000 | 3.74e-01 |
| Pre-NOTCH Processing in Golgi | 14 | 2.08e-02 | -0.357000 | 4.21e-01 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 14 | 2.18e-02 | -0.354000 | 4.21e-01 |
| Aflatoxin activation and detoxification | 16 | 1.44e-02 | -0.353000 | 4.21e-01 |
| SHC1 events in EGFR signaling | 14 | 2.31e-02 | 0.351000 | 4.21e-01 |
| Termination of O-glycan biosynthesis | 19 | 9.85e-03 | -0.342000 | 4.15e-01 |
| PI3K events in ERBB2 signaling | 16 | 1.99e-02 | 0.336000 | 4.21e-01 |
| Activation of RAC1 | 12 | 4.43e-02 | 0.335000 | 5.01e-01 |
| Removal of the Flap Intermediate from the C-strand | 12 | 4.48e-02 | -0.335000 | 5.01e-01 |
| Gluconeogenesis | 29 | 1.87e-03 | -0.334000 | 1.63e-01 |
| Processive synthesis on the lagging strand | 12 | 4.69e-02 | -0.331000 | 5.01e-01 |
| XBP1(S) activates chaperone genes | 42 | 3.05e-04 | -0.322000 | 3.54e-02 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 16 | 2.64e-02 | 0.321000 | 4.21e-01 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 16 | 2.69e-02 | 0.319000 | 4.21e-01 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 16 | 2.69e-02 | 0.319000 | 4.21e-01 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | 13 | 4.67e-02 | 0.319000 | 5.01e-01 |
| Receptor-type tyrosine-protein phosphatases | 19 | 1.62e-02 | 0.319000 | 4.21e-01 |
| Polymerase switching on the C-strand of the telomere | 21 | 1.17e-02 | -0.318000 | 4.21e-01 |
| Constitutive Signaling by EGFRvIII | 15 | 3.36e-02 | 0.317000 | 4.63e-01 |
| Signaling by EGFRvIII in Cancer | 15 | 3.36e-02 | 0.317000 | 4.63e-01 |
| Signaling by EGFR in Cancer | 22 | 1.08e-02 | 0.314000 | 4.21e-01 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 17 | 2.53e-02 | -0.313000 | 4.21e-01 |
| CD209 (DC-SIGN) signaling | 19 | 1.84e-02 | 0.312000 | 4.21e-01 |
| Acyl chain remodelling of PI | 14 | 4.33e-02 | -0.312000 | 5.01e-01 |
| Signaling by Leptin | 10 | 8.82e-02 | -0.311000 | 6.23e-01 |
| Activated NTRK2 signals through FRS2 and FRS3 | 10 | 8.91e-02 | 0.310000 | 6.23e-01 |
| MET activates RAS signaling | 11 | 7.63e-02 | 0.309000 | 5.99e-01 |
| Apoptotic cleavage of cell adhesion proteins | 10 | 9.14e-02 | 0.308000 | 6.29e-01 |
| Nucleobase biosynthesis | 13 | 5.57e-02 | -0.306000 | 5.31e-01 |
| Regulation of TLR by endogenous ligand | 15 | 4.26e-02 | 0.302000 | 5.01e-01 |
| Degradation of cysteine and homocysteine | 11 | 8.49e-02 | -0.300000 | 6.23e-01 |
| IRE1alpha activates chaperones | 44 | 6.20e-04 | -0.298000 | 6.16e-02 |
| ERBB2 Regulates Cell Motility | 14 | 5.63e-02 | 0.295000 | 5.32e-01 |
| Lagging Strand Synthesis | 17 | 3.58e-02 | -0.294000 | 4.69e-01 |
| Signaling by ERBB2 KD Mutants | 24 | 1.33e-02 | 0.292000 | 4.21e-01 |
| Interleukin-20 family signaling | 24 | 1.39e-02 | -0.290000 | 4.21e-01 |
| Signaling by ERBB2 in Cancer | 25 | 1.22e-02 | 0.290000 | 4.21e-01 |
| Fertilization | 22 | 1.91e-02 | -0.289000 | 4.21e-01 |
| Activation of AMPK downstream of NMDARs | 10 | 1.17e-01 | -0.286000 | 6.34e-01 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | 15 | 5.57e-02 | -0.285000 | 5.31e-01 |
| Diseases of hemostasis | 15 | 5.57e-02 | -0.285000 | 5.31e-01 |
| Metabolism of amine-derived hormones | 16 | 4.85e-02 | -0.285000 | 5.07e-01 |
| Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 10 | 1.20e-01 | -0.284000 | 6.34e-01 |
| Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 10 | 1.20e-01 | 0.284000 | 6.34e-01 |
| Caspase activation via Death Receptors in the presence of ligand | 16 | 4.96e-02 | 0.284000 | 5.07e-01 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 24 | 1.64e-02 | 0.283000 | 4.21e-01 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 11 | 1.04e-01 | -0.283000 | 6.34e-01 |
| Carboxyterminal post-translational modifications of tubulin | 35 | 3.89e-03 | -0.282000 | 2.80e-01 |
| Leading Strand Synthesis | 13 | 7.85e-02 | -0.282000 | 6.07e-01 |
| Polymerase switching | 13 | 7.85e-02 | -0.282000 | 6.07e-01 |
| Signaling by ERBB2 TMD/JMD mutants | 21 | 2.54e-02 | 0.282000 | 4.21e-01 |
| Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane | 11 | 1.06e-01 | -0.281000 | 6.34e-01 |
| Acyl chain remodelling of PG | 15 | 6.04e-02 | -0.280000 | 5.60e-01 |
| PINK1-PRKN Mediated Mitophagy | 14 | 7.01e-02 | -0.280000 | 5.84e-01 |
| Synthesis of PE | 10 | 1.26e-01 | -0.279000 | 6.42e-01 |
| ERBB2 Activates PTK6 Signaling | 13 | 8.33e-02 | 0.277000 | 6.20e-01 |
| Citric acid cycle (TCA cycle) | 18 | 4.20e-02 | 0.277000 | 5.01e-01 |
| Deadenylation of mRNA | 20 | 3.21e-02 | 0.277000 | 4.51e-01 |
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) | 11 | 1.15e-01 | -0.275000 | 6.34e-01 |
| Prolonged ERK activation events | 14 | 7.63e-02 | 0.274000 | 5.99e-01 |
| Frs2-mediated activation | 12 | 1.08e-01 | 0.268000 | 6.34e-01 |
| Fanconi Anemia Pathway | 24 | 2.33e-02 | -0.268000 | 4.21e-01 |
| IL-6-type cytokine receptor ligand interactions | 16 | 6.44e-02 | -0.267000 | 5.62e-01 |
| Signaling by FGFR4 in disease | 11 | 1.28e-01 | 0.265000 | 6.43e-01 |
| Xenobiotics | 23 | 2.86e-02 | 0.264000 | 4.33e-01 |
| EGFR downregulation | 28 | 1.58e-02 | 0.264000 | 4.21e-01 |
| Termination of translesion DNA synthesis | 24 | 2.60e-02 | -0.263000 | 4.21e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 12 | 1.15e-01 | -0.263000 | 6.34e-01 |
| Signaling by NODAL | 18 | 5.45e-02 | -0.262000 | 5.31e-01 |
| Cellular hexose transport | 20 | 4.35e-02 | -0.261000 | 5.01e-01 |
| Regulation of PTEN mRNA translation | 14 | 9.39e-02 | 0.259000 | 6.34e-01 |
| Cleavage of the damaged pyrimidine | 13 | 1.08e-01 | -0.258000 | 6.34e-01 |
| Depyrimidination | 13 | 1.08e-01 | -0.258000 | 6.34e-01 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 13 | 1.08e-01 | -0.258000 | 6.34e-01 |
| Glyoxylate metabolism and glycine degradation | 28 | 1.90e-02 | -0.256000 | 4.21e-01 |
| Base-Excision Repair, AP Site Formation | 15 | 8.71e-02 | -0.255000 | 6.23e-01 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 20 | 4.89e-02 | 0.254000 | 5.07e-01 |
| PIWI-interacting RNA (piRNA) biogenesis | 20 | 4.92e-02 | -0.254000 | 5.07e-01 |
| Telomere C-strand (Lagging Strand) Synthesis | 27 | 2.27e-02 | -0.253000 | 4.21e-01 |
| STING mediated induction of host immune responses | 12 | 1.29e-01 | -0.253000 | 6.44e-01 |
| Telomere C-strand synthesis initiation | 10 | 1.72e-01 | -0.250000 | 6.82e-01 |
| Negative regulation of MET activity | 18 | 6.77e-02 | 0.249000 | 5.71e-01 |
| Defective GALNT12 causes colorectal cancer 1 (CRCS1) | 13 | 1.25e-01 | -0.246000 | 6.42e-01 |
| Sulfur amino acid metabolism | 22 | 4.62e-02 | -0.246000 | 5.01e-01 |
| SUMOylation of DNA methylation proteins | 15 | 1.01e-01 | -0.244000 | 6.34e-01 |
| Synthesis of substrates in N-glycan biosythesis | 53 | 2.20e-03 | -0.243000 | 1.70e-01 |
| Sema4D induced cell migration and growth-cone collapse | 19 | 6.72e-02 | -0.243000 | 5.70e-01 |
| Regulation of necroptotic cell death | 13 | 1.30e-01 | 0.243000 | 6.44e-01 |
| Sialic acid metabolism | 28 | 2.68e-02 | -0.242000 | 4.21e-01 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 27 | 2.98e-02 | 0.242000 | 4.42e-01 |
| CLEC7A (Dectin-1) induces NFAT activation | 10 | 1.87e-01 | 0.241000 | 6.82e-01 |
| Cholesterol biosynthesis | 20 | 6.35e-02 | -0.240000 | 5.62e-01 |
| Pausing and recovery of Tat-mediated HIV elongation | 20 | 6.48e-02 | -0.239000 | 5.62e-01 |
| Tat-mediated HIV elongation arrest and recovery | 20 | 6.48e-02 | -0.239000 | 5.62e-01 |
| InlB-mediated entry of Listeria monocytogenes into host cell | 12 | 1.53e-01 | 0.238000 | 6.75e-01 |
| Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | 11 | 1.74e-01 | -0.237000 | 6.82e-01 |
| RMTs methylate histone arginines | 30 | 2.57e-02 | -0.235000 | 4.21e-01 |
| Mismatch Repair | 13 | 1.43e-01 | -0.235000 | 6.70e-01 |
| Signaling by FGFR3 fusions in cancer | 10 | 1.99e-01 | 0.235000 | 6.82e-01 |
| Signaling by ERBB2 ECD mutants | 15 | 1.16e-01 | 0.234000 | 6.34e-01 |
| LGI-ADAM interactions | 13 | 1.44e-01 | -0.234000 | 6.70e-01 |
| Diseases of carbohydrate metabolism | 27 | 3.59e-02 | -0.233000 | 4.69e-01 |
| Regulation of TP53 Activity through Acetylation | 27 | 3.61e-02 | -0.233000 | 4.69e-01 |
| DSCAM interactions | 11 | 1.82e-01 | 0.232000 | 6.82e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 12 | 1.63e-01 | -0.232000 | 6.75e-01 |
| Processing of SMDT1 | 11 | 1.83e-01 | -0.232000 | 6.82e-01 |
| The NLRP3 inflammasome | 13 | 1.49e-01 | -0.231000 | 6.74e-01 |
| Interleukin-2 signaling | 11 | 1.84e-01 | -0.231000 | 6.82e-01 |
| Amino acid transport across the plasma membrane | 31 | 2.63e-02 | -0.231000 | 4.21e-01 |
| Signaling by FGFR3 in disease | 22 | 6.30e-02 | 0.229000 | 5.62e-01 |
| Signaling by FGFR3 point mutants in cancer | 22 | 6.30e-02 | 0.229000 | 5.62e-01 |
| Spry regulation of FGF signaling | 13 | 1.57e-01 | 0.227000 | 6.75e-01 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 11 | 1.94e-01 | 0.226000 | 6.82e-01 |
| Apoptotic factor-mediated response | 12 | 1.77e-01 | -0.225000 | 6.82e-01 |
| Creatine metabolism | 10 | 2.18e-01 | -0.225000 | 6.93e-01 |
| Pyrimidine catabolism | 11 | 1.97e-01 | 0.225000 | 6.82e-01 |
| Protein ubiquitination | 42 | 1.21e-02 | 0.224000 | 4.21e-01 |
| Translocation of ZAP-70 to Immunological synapse | 12 | 1.80e-01 | -0.224000 | 6.82e-01 |
| Signaling by FGFR3 | 36 | 2.07e-02 | 0.223000 | 4.21e-01 |
| Establishment of Sister Chromatid Cohesion | 10 | 2.25e-01 | 0.222000 | 6.94e-01 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 65 | 2.03e-03 | -0.221000 | 1.66e-01 |
| Signaling by Activin | 12 | 1.87e-01 | 0.220000 | 6.82e-01 |
| Transport of organic anions | 11 | 2.07e-01 | 0.220000 | 6.87e-01 |
| Role of LAT2/NTAL/LAB on calcium mobilization | 17 | 1.17e-01 | 0.220000 | 6.34e-01 |
| Interleukin-6 family signaling | 23 | 6.84e-02 | -0.220000 | 5.73e-01 |
| Translation of Replicase and Assembly of the Replication Transcription Complex | 11 | 2.09e-01 | -0.219000 | 6.87e-01 |
| Post-chaperonin tubulin folding pathway | 22 | 8.00e-02 | -0.216000 | 6.10e-01 |
| MECP2 regulates neuronal receptors and channels | 17 | 1.25e-01 | 0.215000 | 6.42e-01 |
| Erythrocytes take up carbon dioxide and release oxygen | 11 | 2.20e-01 | 0.214000 | 6.93e-01 |
| O2/CO2 exchange in erythrocytes | 11 | 2.20e-01 | 0.214000 | 6.93e-01 |
| RHO GTPases Activate NADPH Oxidases | 23 | 7.67e-02 | -0.213000 | 5.99e-01 |
| Signaling by FGFR2 | 61 | 4.02e-03 | 0.213000 | 2.80e-01 |
| Synthesis of PIPs at the late endosome membrane | 10 | 2.47e-01 | 0.212000 | 7.11e-01 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 18 | 1.20e-01 | 0.212000 | 6.34e-01 |
| Regulation of beta-cell development | 36 | 2.85e-02 | 0.211000 | 4.33e-01 |
| Mitophagy | 20 | 1.03e-01 | -0.211000 | 6.34e-01 |
| PKA-mediated phosphorylation of CREB | 19 | 1.12e-01 | 0.210000 | 6.34e-01 |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | 10 | 2.49e-01 | -0.210000 | 7.11e-01 |
| Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) | 11 | 2.28e-01 | 0.210000 | 6.97e-01 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 14 | 1.75e-01 | 0.209000 | 6.82e-01 |
| WNT5A-dependent internalization of FZD4 | 14 | 1.77e-01 | -0.208000 | 6.82e-01 |
| PD-1 signaling | 15 | 1.64e-01 | -0.208000 | 6.75e-01 |
| Regulation of TP53 Activity through Methylation | 13 | 1.97e-01 | -0.207000 | 6.82e-01 |
| Sodium/Calcium exchangers | 10 | 2.59e-01 | 0.206000 | 7.11e-01 |
| Acyl chain remodelling of PC | 23 | 8.73e-02 | -0.206000 | 6.23e-01 |
| Other interleukin signaling | 20 | 1.12e-01 | -0.205000 | 6.34e-01 |
| Selective autophagy | 50 | 1.22e-02 | -0.205000 | 4.21e-01 |
| Defective GALNT3 causes familial hyperphosphatemic tumoral calcinosis (HFTC) | 13 | 2.01e-01 | -0.205000 | 6.82e-01 |
| Kinesins | 39 | 2.73e-02 | -0.204000 | 4.21e-01 |
| E3 ubiquitin ligases ubiquitinate target proteins | 26 | 7.25e-02 | 0.204000 | 5.97e-01 |
| POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | 11 | 2.44e-01 | -0.203000 | 7.10e-01 |
| Signal regulatory protein family interactions | 13 | 2.06e-01 | 0.203000 | 6.87e-01 |
| The canonical retinoid cycle in rods (twilight vision) | 20 | 1.17e-01 | -0.203000 | 6.34e-01 |
| HDACs deacetylate histones | 26 | 7.39e-02 | -0.203000 | 5.99e-01 |
| Gastrin-CREB signalling pathway via PKC and MAPK | 18 | 1.37e-01 | 0.202000 | 6.63e-01 |
| Regulation of pyruvate dehydrogenase (PDH) complex | 13 | 2.07e-01 | -0.202000 | 6.87e-01 |
| VLDLR internalisation and degradation | 12 | 2.28e-01 | -0.201000 | 6.97e-01 |
| Processive synthesis on the C-strand of the telomere | 14 | 1.93e-01 | -0.201000 | 6.82e-01 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 13 | 2.10e-01 | 0.201000 | 6.87e-01 |
| Signaling by FGFR1 | 45 | 1.99e-02 | 0.201000 | 4.21e-01 |
| Downstream signaling of activated FGFR3 | 24 | 8.93e-02 | 0.200000 | 6.23e-01 |
| Regulation of commissural axon pathfinding by SLIT and ROBO | 10 | 2.74e-01 | 0.200000 | 7.27e-01 |
| Gap junction assembly | 16 | 1.67e-01 | -0.200000 | 6.77e-01 |
| Striated Muscle Contraction | 33 | 4.71e-02 | -0.200000 | 5.01e-01 |
| IRF3-mediated induction of type I IFN | 10 | 2.75e-01 | -0.199000 | 7.27e-01 |
| Hyaluronan uptake and degradation | 11 | 2.53e-01 | -0.199000 | 7.11e-01 |
| GPCR downstream signalling | 920 | 3.51e-24 | 0.198000 | 1.63e-21 |
| Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS) | 14 | 1.99e-01 | -0.198000 | 6.82e-01 |
| Dual Incision in GG-NER | 34 | 4.58e-02 | -0.198000 | 5.01e-01 |
| Recycling of bile acids and salts | 15 | 1.85e-01 | 0.198000 | 6.82e-01 |
| CASP8 activity is inhibited | 11 | 2.58e-01 | 0.197000 | 7.11e-01 |
| Dimerization of procaspase-8 | 11 | 2.58e-01 | 0.197000 | 7.11e-01 |
| Regulation by c-FLIP | 11 | 2.58e-01 | 0.197000 | 7.11e-01 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 14 | 2.03e-01 | -0.196000 | 6.86e-01 |
| Tight junction interactions | 28 | 7.25e-02 | -0.196000 | 5.97e-01 |
| Acyl chain remodelling of PE | 21 | 1.20e-01 | -0.196000 | 6.34e-01 |
| HIV elongation arrest and recovery | 21 | 1.20e-01 | -0.196000 | 6.34e-01 |
| Pausing and recovery of HIV elongation | 21 | 1.20e-01 | -0.196000 | 6.34e-01 |
| FCERI mediated MAPK activation | 31 | 5.94e-02 | 0.196000 | 5.58e-01 |
| Nephrin family interactions | 21 | 1.22e-01 | 0.195000 | 6.39e-01 |
| Signaling by EGFR | 46 | 2.21e-02 | 0.195000 | 4.21e-01 |
| FGFR2 alternative splicing | 19 | 1.42e-01 | 0.195000 | 6.70e-01 |
| Ketone body metabolism | 10 | 2.87e-01 | -0.194000 | 7.27e-01 |
| Metalloprotease DUBs | 17 | 1.70e-01 | 0.192000 | 6.82e-01 |
| Sema4D in semaphorin signaling | 22 | 1.19e-01 | -0.192000 | 6.34e-01 |
| Repression of WNT target genes | 12 | 2.53e-01 | -0.191000 | 7.11e-01 |
| Processing of Capped Intronless Pre-mRNA | 19 | 1.50e-01 | 0.191000 | 6.74e-01 |
| Signaling by GPCR | 976 | 2.34e-23 | 0.190000 | 8.13e-21 |
| ROS and RNS production in phagocytes | 33 | 6.17e-02 | -0.188000 | 5.61e-01 |
| Keratan sulfate degradation | 10 | 3.05e-01 | 0.187000 | 7.39e-01 |
| Listeria monocytogenes entry into host cells | 17 | 1.82e-01 | 0.187000 | 6.82e-01 |
| Synthesis of bile acids and bile salts via 27-hydroxycholesterol | 11 | 2.83e-01 | -0.187000 | 7.27e-01 |
| Depolymerisation of the Nuclear Lamina | 14 | 2.26e-01 | -0.187000 | 6.97e-01 |
| Transcriptional Regulation by MECP2 | 55 | 1.66e-02 | 0.187000 | 4.21e-01 |
| Purine ribonucleoside monophosphate biosynthesis | 11 | 2.83e-01 | -0.187000 | 7.27e-01 |
| Regulation of innate immune responses to cytosolic DNA | 11 | 2.84e-01 | -0.186000 | 7.27e-01 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 11 | 2.86e-01 | -0.186000 | 7.27e-01 |
| alpha-linolenic acid (ALA) metabolism | 11 | 2.86e-01 | -0.186000 | 7.27e-01 |
| Incretin synthesis, secretion, and inactivation | 21 | 1.41e-01 | 0.185000 | 6.70e-01 |
| Regulation of signaling by NODAL | 10 | 3.10e-01 | -0.185000 | 7.39e-01 |
| Downstream signaling of activated FGFR2 | 29 | 8.46e-02 | 0.185000 | 6.23e-01 |
| Activation of the phototransduction cascade | 11 | 2.88e-01 | -0.185000 | 7.27e-01 |
| tRNA modification in the nucleus and cytosol | 31 | 7.50e-02 | -0.185000 | 5.99e-01 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | 19 | 1.64e-01 | -0.184000 | 6.75e-01 |
| Neurodegenerative Diseases | 19 | 1.64e-01 | -0.184000 | 6.75e-01 |
| Cell recruitment (pro-inflammatory response) | 21 | 1.44e-01 | -0.184000 | 6.70e-01 |
| Purinergic signaling in leishmaniasis infection | 21 | 1.44e-01 | -0.184000 | 6.70e-01 |
| Peroxisomal lipid metabolism | 26 | 1.04e-01 | -0.184000 | 6.34e-01 |
| MicroRNA (miRNA) biogenesis | 15 | 2.17e-01 | -0.184000 | 6.93e-01 |
| Diseases of programmed cell death | 20 | 1.55e-01 | -0.184000 | 6.75e-01 |
| Neurotoxicity of clostridium toxins | 10 | 3.15e-01 | -0.183000 | 7.39e-01 |
| Dopamine Neurotransmitter Release Cycle | 19 | 1.66e-01 | 0.183000 | 6.77e-01 |
| FGFRL1 modulation of FGFR1 signaling | 13 | 2.54e-01 | 0.183000 | 7.11e-01 |
| IKK complex recruitment mediated by RIP1 | 17 | 1.93e-01 | 0.183000 | 6.82e-01 |
| Uptake and actions of bacterial toxins | 29 | 8.90e-02 | -0.182000 | 6.23e-01 |
| RIPK1-mediated regulated necrosis | 15 | 2.22e-01 | 0.182000 | 6.94e-01 |
| Regulated Necrosis | 15 | 2.22e-01 | 0.182000 | 6.94e-01 |
| Zinc transporters | 14 | 2.39e-01 | -0.182000 | 7.09e-01 |
| Pyruvate metabolism | 25 | 1.19e-01 | -0.180000 | 6.34e-01 |
| Reproduction | 74 | 7.67e-03 | -0.179000 | 3.74e-01 |
| Lysosome Vesicle Biogenesis | 30 | 8.98e-02 | -0.179000 | 6.23e-01 |
| SHC-mediated cascade:FGFR3 | 18 | 1.90e-01 | 0.178000 | 6.82e-01 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | 16 | 2.18e-01 | -0.178000 | 6.93e-01 |
| Netrin-1 signaling | 49 | 3.18e-02 | 0.177000 | 4.51e-01 |
| Syndecan interactions | 17 | 2.06e-01 | -0.177000 | 6.87e-01 |
| Other semaphorin interactions | 18 | 1.96e-01 | 0.176000 | 6.82e-01 |
| Ras activation upon Ca2+ influx through NMDA receptor | 19 | 1.84e-01 | 0.176000 | 6.82e-01 |
| NR1H2 and NR1H3-mediated signaling | 44 | 4.36e-02 | -0.176000 | 5.01e-01 |
| RHO GTPases activate CIT | 18 | 1.97e-01 | -0.176000 | 6.82e-01 |
| Carnitine metabolism | 11 | 3.13e-01 | -0.176000 | 7.39e-01 |
| Caspase activation via extrinsic apoptotic signalling pathway | 24 | 1.37e-01 | 0.175000 | 6.63e-01 |
| Gamma-carboxylation of protein precursors | 10 | 3.38e-01 | -0.175000 | 7.61e-01 |
| Pregnenolone biosynthesis | 10 | 3.39e-01 | -0.175000 | 7.61e-01 |
| RAS processing | 17 | 2.13e-01 | 0.174000 | 6.93e-01 |
| Synthesis of PIPs at the early endosome membrane | 15 | 2.43e-01 | 0.174000 | 7.09e-01 |
| FRS-mediated FGFR3 signaling | 19 | 1.89e-01 | 0.174000 | 6.82e-01 |
| DNA strand elongation | 26 | 1.27e-01 | -0.173000 | 6.43e-01 |
| Inhibition of DNA recombination at telomere | 13 | 2.81e-01 | -0.173000 | 7.27e-01 |
| Glycogen storage diseases | 11 | 3.22e-01 | -0.173000 | 7.46e-01 |
| Pre-NOTCH Expression and Processing | 46 | 4.30e-02 | -0.173000 | 5.01e-01 |
| Negative regulation of TCF-dependent signaling by WNT ligand antagonists | 14 | 2.64e-01 | 0.172000 | 7.16e-01 |
| RNA Polymerase I Transcription | 40 | 5.97e-02 | -0.172000 | 5.58e-01 |
| Adenylate cyclase inhibitory pathway | 14 | 2.65e-01 | 0.172000 | 7.17e-01 |
| TP53 Regulates Transcription of Death Receptors and Ligands | 12 | 3.02e-01 | 0.172000 | 7.37e-01 |
| Serotonin receptors | 11 | 3.25e-01 | 0.171000 | 7.49e-01 |
| SHC1 events in ERBB2 signaling | 22 | 1.65e-01 | 0.171000 | 6.77e-01 |
| Synthesis of PIPs at the Golgi membrane | 17 | 2.23e-01 | 0.171000 | 6.94e-01 |
| HS-GAG biosynthesis | 26 | 1.32e-01 | 0.171000 | 6.51e-01 |
| RNA Polymerase I Promoter Clearance | 39 | 6.58e-02 | -0.170000 | 5.62e-01 |
| Trafficking of GluR2-containing AMPA receptors | 15 | 2.54e-01 | -0.170000 | 7.11e-01 |
| Synthesis of IP2, IP, and Ins in the cytosol | 14 | 2.70e-01 | -0.170000 | 7.26e-01 |
| Negative regulation of FGFR3 signaling | 26 | 1.34e-01 | 0.170000 | 6.59e-01 |
| RUNX2 regulates bone development | 30 | 1.09e-01 | 0.169000 | 6.34e-01 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 36 | 8.02e-02 | -0.169000 | 6.10e-01 |
| NCAM1 interactions | 35 | 8.54e-02 | -0.168000 | 6.23e-01 |
| Signaling by FGFR | 73 | 1.31e-02 | 0.168000 | 4.21e-01 |
| Resolution of Abasic Sites (AP sites) | 31 | 1.06e-01 | -0.168000 | 6.34e-01 |
| GABA receptor activation | 52 | 3.66e-02 | 0.168000 | 4.71e-01 |
| TICAM1, RIP1-mediated IKK complex recruitment | 13 | 2.96e-01 | 0.167000 | 7.32e-01 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 34 | 9.62e-02 | -0.165000 | 6.34e-01 |
| Activation of NMDA receptors and postsynaptic events | 72 | 1.59e-02 | 0.164000 | 4.21e-01 |
| Initial triggering of complement | 27 | 1.40e-01 | -0.164000 | 6.70e-01 |
| SHC-mediated cascade:FGFR2 | 23 | 1.74e-01 | 0.164000 | 6.82e-01 |
| Positive epigenetic regulation of rRNA expression | 36 | 9.00e-02 | -0.163000 | 6.23e-01 |
| Signaling by ERBB4 | 52 | 4.23e-02 | 0.163000 | 5.01e-01 |
| Cyclin A/B1/B2 associated events during G2/M transition | 21 | 1.97e-01 | 0.163000 | 6.82e-01 |
| Signaling by Non-Receptor Tyrosine Kinases | 47 | 5.36e-02 | 0.163000 | 5.31e-01 |
| Signaling by PTK6 | 47 | 5.36e-02 | 0.163000 | 5.31e-01 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | 28 | 1.36e-01 | -0.163000 | 6.62e-01 |
| Regulation of RUNX3 expression and activity | 43 | 6.58e-02 | -0.162000 | 5.62e-01 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | 47 | 5.50e-02 | -0.162000 | 5.31e-01 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 35 | 9.80e-02 | -0.162000 | 6.34e-01 |
| Meiotic synapsis | 30 | 1.26e-01 | -0.161000 | 6.42e-01 |
| RNA Polymerase I Transcription Initiation | 36 | 9.40e-02 | -0.161000 | 6.34e-01 |
| FRS-mediated FGFR2 signaling | 24 | 1.72e-01 | 0.161000 | 6.82e-01 |
| Glycosphingolipid metabolism | 36 | 9.49e-02 | -0.161000 | 6.34e-01 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 13 | 3.16e-01 | -0.161000 | 7.39e-01 |
| Glycerophospholipid biosynthesis | 104 | 4.71e-03 | -0.161000 | 2.97e-01 |
| Negative regulation of FGFR2 signaling | 31 | 1.22e-01 | 0.160000 | 6.39e-01 |
| Insulin processing | 22 | 1.93e-01 | 0.160000 | 6.82e-01 |
| SUMOylation of transcription factors | 16 | 2.67e-01 | -0.160000 | 7.20e-01 |
| Metal ion SLC transporters | 21 | 2.05e-01 | -0.160000 | 6.87e-01 |
| Formation of the beta-catenin:TCF transactivating complex | 30 | 1.30e-01 | -0.160000 | 6.44e-01 |
| Regulation of gene expression in beta cells | 18 | 2.41e-01 | 0.160000 | 7.09e-01 |
| Bicarbonate transporters | 10 | 3.83e-01 | -0.159000 | 7.82e-01 |
| Plasma lipoprotein clearance | 32 | 1.19e-01 | -0.159000 | 6.34e-01 |
| DAP12 signaling | 26 | 1.61e-01 | 0.159000 | 6.75e-01 |
| Signaling by FGFR4 | 36 | 9.90e-02 | 0.159000 | 6.34e-01 |
| Plasma lipoprotein remodeling | 28 | 1.48e-01 | -0.158000 | 6.74e-01 |
| PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 12 | 3.45e-01 | 0.158000 | 7.62e-01 |
| TRAF6 mediated NF-kB activation | 20 | 2.24e-01 | -0.157000 | 6.94e-01 |
| FGFR2 ligand binding and activation | 19 | 2.36e-01 | 0.157000 | 7.09e-01 |
| Retrograde transport at the Trans-Golgi-Network | 41 | 8.34e-02 | 0.156000 | 6.20e-01 |
| Base Excision Repair | 37 | 1.02e-01 | -0.155000 | 6.34e-01 |
| PI-3K cascade:FGFR3 | 18 | 2.55e-01 | 0.155000 | 7.11e-01 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 18 | 2.57e-01 | 0.154000 | 7.11e-01 |
| Basigin interactions | 24 | 1.91e-01 | -0.154000 | 6.82e-01 |
| MAPK targets/ Nuclear events mediated by MAP kinases | 30 | 1.44e-01 | 0.154000 | 6.70e-01 |
| PCNA-Dependent Long Patch Base Excision Repair | 17 | 2.73e-01 | -0.154000 | 7.27e-01 |
| Platelet Adhesion to exposed collagen | 13 | 3.39e-01 | 0.153000 | 7.61e-01 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | 19 | 2.48e-01 | 0.153000 | 7.11e-01 |
| Synaptic adhesion-like molecules | 21 | 2.25e-01 | -0.153000 | 6.94e-01 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 29 | 1.54e-01 | -0.153000 | 6.75e-01 |
| Gap junction trafficking | 24 | 1.95e-01 | -0.153000 | 6.82e-01 |
| Fatty acids | 11 | 3.84e-01 | 0.152000 | 7.82e-01 |
| Notch-HLH transcription pathway | 24 | 1.98e-01 | -0.152000 | 6.82e-01 |
| Organic cation/anion/zwitterion transport | 14 | 3.26e-01 | -0.152000 | 7.49e-01 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | 27 | 1.73e-01 | -0.152000 | 6.82e-01 |
| Signaling by Retinoic Acid | 40 | 9.72e-02 | -0.152000 | 6.34e-01 |
| AKT phosphorylates targets in the cytosol | 13 | 3.44e-01 | -0.152000 | 7.62e-01 |
| Response of Mtb to phagocytosis | 20 | 2.42e-01 | 0.151000 | 7.09e-01 |
| Integrin cell surface interactions | 61 | 4.18e-02 | -0.151000 | 5.01e-01 |
| PKA activation | 17 | 2.85e-01 | 0.150000 | 7.27e-01 |
| Gap junction trafficking and regulation | 26 | 1.86e-01 | -0.150000 | 6.82e-01 |
| Activation of gene expression by SREBF (SREBP) | 39 | 1.07e-01 | -0.149000 | 6.34e-01 |
| Glucose metabolism | 77 | 2.38e-02 | -0.149000 | 4.21e-01 |
| DNA Double Strand Break Response | 36 | 1.25e-01 | -0.148000 | 6.42e-01 |
| Resolution of D-Loop Structures | 29 | 1.68e-01 | -0.148000 | 6.82e-01 |
| Reduction of cytosolic Ca++ levels | 12 | 3.75e-01 | 0.148000 | 7.82e-01 |
| Suppression of phagosomal maturation | 10 | 4.19e-01 | 0.148000 | 7.95e-01 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 38 | 1.16e-01 | 0.147000 | 6.34e-01 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 30 | 1.63e-01 | -0.147000 | 6.75e-01 |
| HIV Transcription Elongation | 30 | 1.63e-01 | -0.147000 | 6.75e-01 |
| Tat-mediated elongation of the HIV-1 transcript | 30 | 1.63e-01 | -0.147000 | 6.75e-01 |
| Processing of Intronless Pre-mRNAs | 12 | 3.78e-01 | 0.147000 | 7.82e-01 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 18 | 2.82e-01 | -0.146000 | 7.27e-01 |
| NRAGE signals death through JNK | 58 | 5.44e-02 | -0.146000 | 5.31e-01 |
| Platelet sensitization by LDL | 16 | 3.12e-01 | -0.146000 | 7.39e-01 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 62 | 4.72e-02 | 0.146000 | 5.01e-01 |
| Class I peroxisomal membrane protein import | 16 | 3.13e-01 | 0.146000 | 7.39e-01 |
| Platelet Aggregation (Plug Formation) | 37 | 1.25e-01 | -0.146000 | 6.42e-01 |
| PI-3K cascade:FGFR2 | 23 | 2.27e-01 | 0.146000 | 6.97e-01 |
| Downstream signaling of activated FGFR1 | 30 | 1.69e-01 | 0.145000 | 6.82e-01 |
| Assembly and cell surface presentation of NMDA receptors | 24 | 2.19e-01 | 0.145000 | 6.93e-01 |
| Assembly of active LPL and LIPC lipase complexes | 18 | 2.88e-01 | -0.145000 | 7.27e-01 |
| Autodegradation of Cdh1 by Cdh1:APC/C | 51 | 7.44e-02 | -0.144000 | 5.99e-01 |
| Cyclin D associated events in G1 | 41 | 1.11e-01 | 0.144000 | 6.34e-01 |
| G1 Phase | 41 | 1.11e-01 | 0.144000 | 6.34e-01 |
| COPI-dependent Golgi-to-ER retrograde traffic | 72 | 3.48e-02 | -0.144000 | 4.69e-01 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 28 | 1.88e-01 | -0.144000 | 6.82e-01 |
| Trafficking of AMPA receptors | 28 | 1.88e-01 | -0.144000 | 6.82e-01 |
| Cell death signalling via NRAGE, NRIF and NADE | 68 | 4.03e-02 | -0.144000 | 5.01e-01 |
| HDMs demethylate histones | 19 | 2.78e-01 | 0.144000 | 7.27e-01 |
| Non-integrin membrane-ECM interactions | 38 | 1.26e-01 | -0.143000 | 6.42e-01 |
| DAP12 interactions | 32 | 1.63e-01 | 0.142000 | 6.75e-01 |
| Aquaporin-mediated transport | 45 | 9.93e-02 | -0.142000 | 6.34e-01 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 12 | 3.94e-01 | 0.142000 | 7.84e-01 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 15 | 3.42e-01 | 0.142000 | 7.61e-01 |
| RUNX2 regulates osteoblast differentiation | 24 | 2.31e-01 | 0.141000 | 7.03e-01 |
| Mitochondrial calcium ion transport | 17 | 3.14e-01 | -0.141000 | 7.39e-01 |
| Surfactant metabolism | 21 | 2.64e-01 | -0.141000 | 7.16e-01 |
| EPHA-mediated growth cone collapse | 14 | 3.62e-01 | -0.141000 | 7.71e-01 |
| Phase II - Conjugation of compounds | 87 | 2.40e-02 | 0.140000 | 4.21e-01 |
| Activated NOTCH1 Transmits Signal to the Nucleus | 24 | 2.37e-01 | -0.139000 | 7.09e-01 |
| Signaling by BMP | 26 | 2.19e-01 | 0.139000 | 6.93e-01 |
| Telomere Extension By Telomerase | 20 | 2.82e-01 | 0.139000 | 7.27e-01 |
| Signaling by NTRK2 (TRKB) | 24 | 2.39e-01 | 0.139000 | 7.09e-01 |
| Voltage gated Potassium channels | 41 | 1.24e-01 | 0.139000 | 6.42e-01 |
| Apoptotic cleavage of cellular proteins | 35 | 1.56e-01 | 0.139000 | 6.75e-01 |
| CD28 dependent Vav1 pathway | 12 | 4.07e-01 | 0.138000 | 7.88e-01 |
| Hyaluronan metabolism | 15 | 3.54e-01 | -0.138000 | 7.68e-01 |
| Stabilization of p53 | 44 | 1.13e-01 | -0.138000 | 6.34e-01 |
| FCERI mediated Ca+2 mobilization | 30 | 1.92e-01 | 0.138000 | 6.82e-01 |
| Thrombin signalling through proteinase activated receptors (PARs) | 27 | 2.16e-01 | -0.138000 | 6.93e-01 |
| rRNA modification in the nucleus and cytosol | 47 | 1.04e-01 | -0.137000 | 6.34e-01 |
| Extra-nuclear estrogen signaling | 69 | 4.90e-02 | 0.137000 | 5.07e-01 |
| Signaling by FGFR2 IIIa TM | 12 | 4.11e-01 | -0.137000 | 7.92e-01 |
| Synthesis of IP3 and IP4 in the cytosol | 23 | 2.57e-01 | -0.137000 | 7.11e-01 |
| MAP kinase activation | 57 | 7.60e-02 | 0.136000 | 5.99e-01 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 39 | 1.45e-01 | -0.135000 | 6.70e-01 |
| Glucocorticoid biosynthesis | 10 | 4.61e-01 | 0.135000 | 8.24e-01 |
| Regulation of gene expression by Hypoxia-inducible Factor | 11 | 4.39e-01 | 0.135000 | 8.10e-01 |
| RNA Polymerase II Transcription Termination | 49 | 1.03e-01 | 0.135000 | 6.34e-01 |
| PCP/CE pathway | 77 | 4.17e-02 | -0.134000 | 5.01e-01 |
| Metabolism of steroid hormones | 31 | 1.96e-01 | -0.134000 | 6.82e-01 |
| Interleukin-27 signaling | 11 | 4.42e-01 | -0.134000 | 8.13e-01 |
| Integrin signaling | 27 | 2.29e-01 | -0.134000 | 6.98e-01 |
| FGFR3 ligand binding and activation | 13 | 4.05e-01 | 0.134000 | 7.88e-01 |
| FGFR3c ligand binding and activation | 13 | 4.05e-01 | 0.134000 | 7.88e-01 |
| Transcription of E2F targets under negative control by DREAM complex | 17 | 3.41e-01 | -0.133000 | 7.61e-01 |
| HDR through Single Strand Annealing (SSA) | 31 | 2.00e-01 | -0.133000 | 6.82e-01 |
| Elevation of cytosolic Ca2+ levels | 14 | 3.89e-01 | -0.133000 | 7.84e-01 |
| DCC mediated attractive signaling | 14 | 3.91e-01 | 0.133000 | 7.84e-01 |
| Meiosis | 52 | 9.84e-02 | -0.133000 | 6.34e-01 |
| Activation of Ca-permeable Kainate Receptor | 10 | 4.70e-01 | 0.132000 | 8.30e-01 |
| Ionotropic activity of kainate receptors | 10 | 4.70e-01 | 0.132000 | 8.30e-01 |
| Unfolded Protein Response (UPR) | 79 | 4.31e-02 | -0.132000 | 5.01e-01 |
| Phospholipase C-mediated cascade; FGFR3 | 13 | 4.12e-01 | 0.131000 | 7.92e-01 |
| HSF1 activation | 21 | 2.98e-01 | -0.131000 | 7.34e-01 |
| Signaling by FGFR2 in disease | 36 | 1.74e-01 | 0.131000 | 6.82e-01 |
| Metabolism of amino acids and derivatives | 285 | 1.68e-04 | -0.130000 | 2.33e-02 |
| Downregulation of ERBB2 signaling | 23 | 2.82e-01 | 0.130000 | 7.27e-01 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | 18 | 3.41e-01 | -0.130000 | 7.61e-01 |
| p75 NTR receptor-mediated signalling | 84 | 4.07e-02 | -0.129000 | 5.01e-01 |
| Regulation of TP53 Activity | 141 | 8.43e-03 | -0.129000 | 3.74e-01 |
| Prostacyclin signalling through prostacyclin receptor | 14 | 4.07e-01 | -0.128000 | 7.88e-01 |
| Chondroitin sulfate biosynthesis | 20 | 3.22e-01 | 0.128000 | 7.46e-01 |
| Transcriptional regulation of granulopoiesis | 31 | 2.18e-01 | -0.128000 | 6.93e-01 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 60 | 8.69e-02 | -0.128000 | 6.23e-01 |
| Gamma carboxylation, hypusine formation and arylsulfatase activation | 31 | 2.21e-01 | -0.127000 | 6.94e-01 |
| Nucleotide salvage | 19 | 3.42e-01 | -0.126000 | 7.61e-01 |
| PKMTs methylate histone lysines | 35 | 1.98e-01 | -0.126000 | 6.82e-01 |
| G alpha (12/13) signalling events | 72 | 6.49e-02 | -0.126000 | 5.62e-01 |
| Phospholipase C-mediated cascade; FGFR2 | 18 | 3.56e-01 | 0.126000 | 7.68e-01 |
| FCGR3A-mediated IL10 synthesis | 44 | 1.50e-01 | 0.125000 | 6.74e-01 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 19 | 3.45e-01 | -0.125000 | 7.62e-01 |
| Apoptotic execution phase | 42 | 1.61e-01 | 0.125000 | 6.75e-01 |
| Interferon gamma signaling | 66 | 7.94e-02 | -0.125000 | 6.10e-01 |
| Synthesis, secretion, and deacylation of Ghrelin | 17 | 3.73e-01 | 0.125000 | 7.82e-01 |
| Infection with Mycobacterium tuberculosis | 24 | 2.90e-01 | 0.125000 | 7.27e-01 |
| Meiotic recombination | 24 | 2.92e-01 | -0.124000 | 7.30e-01 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 15 | 4.06e-01 | 0.124000 | 7.88e-01 |
| Cross-presentation of soluble exogenous antigens (endosomes) | 42 | 1.66e-01 | -0.124000 | 6.77e-01 |
| Activation of SMO | 14 | 4.24e-01 | -0.123000 | 7.97e-01 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 81 | 5.53e-02 | -0.123000 | 5.31e-01 |
| Erythropoietin activates RAS | 13 | 4.46e-01 | 0.122000 | 8.13e-01 |
| Diseases associated with O-glycosylation of proteins | 57 | 1.12e-01 | -0.122000 | 6.34e-01 |
| Formation of HIV elongation complex in the absence of HIV Tat | 31 | 2.43e-01 | -0.121000 | 7.09e-01 |
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 20 | 3.49e-01 | -0.121000 | 7.68e-01 |
| Hh mutants that don't undergo autocatalytic processing are degraded by ERAD | 42 | 1.76e-01 | -0.121000 | 6.82e-01 |
| Downregulation of TGF-beta receptor signaling | 20 | 3.50e-01 | 0.121000 | 7.68e-01 |
| Downstream signaling of activated FGFR4 | 25 | 2.98e-01 | 0.120000 | 7.34e-01 |
| mRNA decay by 5' to 3' exoribonuclease | 13 | 4.53e-01 | -0.120000 | 8.18e-01 |
| Transport of vitamins, nucleosides, and related molecules | 37 | 2.07e-01 | -0.120000 | 6.87e-01 |
| Autophagy | 108 | 3.18e-02 | -0.120000 | 4.51e-01 |
| Macroautophagy | 95 | 4.42e-02 | -0.120000 | 5.01e-01 |
| ADP signalling through P2Y purinoceptor 12 | 17 | 3.94e-01 | 0.120000 | 7.84e-01 |
| ERKs are inactivated | 13 | 4.56e-01 | -0.119000 | 8.20e-01 |
| Myogenesis | 27 | 2.83e-01 | 0.119000 | 7.27e-01 |
| Blood group systems biosynthesis | 15 | 4.24e-01 | -0.119000 | 7.97e-01 |
| Assembly Of The HIV Virion | 11 | 4.93e-01 | -0.119000 | 8.47e-01 |
| Laminin interactions | 23 | 3.23e-01 | -0.119000 | 7.47e-01 |
| Translesion synthesis by POLI | 13 | 4.57e-01 | -0.119000 | 8.21e-01 |
| Asymmetric localization of PCP proteins | 53 | 1.35e-01 | -0.119000 | 6.62e-01 |
| Autodegradation of the E3 ubiquitin ligase COP1 | 41 | 1.90e-01 | -0.118000 | 6.82e-01 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | 20 | 3.60e-01 | -0.118000 | 7.70e-01 |
| APC/C:Cdc20 mediated degradation of Securin | 55 | 1.30e-01 | -0.118000 | 6.44e-01 |
| Transcriptional regulation by RUNX3 | 82 | 6.56e-02 | -0.118000 | 5.62e-01 |
| KSRP (KHSRP) binds and destabilizes mRNA | 15 | 4.30e-01 | -0.118000 | 8.04e-01 |
| Translesion synthesis by REV1 | 12 | 4.81e-01 | -0.118000 | 8.42e-01 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 19 | 3.75e-01 | -0.117000 | 7.82e-01 |
| Plasma lipoprotein assembly, remodeling, and clearance | 63 | 1.09e-01 | -0.117000 | 6.34e-01 |
| Elastic fibre formation | 37 | 2.20e-01 | -0.116000 | 6.94e-01 |
| p38MAPK events | 13 | 4.67e-01 | -0.116000 | 8.28e-01 |
| HSF1-dependent transactivation | 28 | 2.87e-01 | -0.116000 | 7.27e-01 |
| Chromatin modifying enzymes | 173 | 8.61e-03 | -0.116000 | 3.74e-01 |
| Chromatin organization | 173 | 8.61e-03 | -0.116000 | 3.74e-01 |
| Defective B3GAT3 causes JDSSDHD | 19 | 3.83e-01 | 0.116000 | 7.82e-01 |
| Tryptophan catabolism | 12 | 4.90e-01 | -0.115000 | 8.44e-01 |
| Phase 2 - plateau phase | 21 | 3.62e-01 | -0.115000 | 7.70e-01 |
| Interleukin receptor SHC signaling | 24 | 3.30e-01 | -0.115000 | 7.52e-01 |
| Mitochondrial tRNA aminoacylation | 15 | 4.43e-01 | -0.114000 | 8.13e-01 |
| Unblocking of NMDA receptors, glutamate binding and activation | 20 | 3.78e-01 | 0.114000 | 7.82e-01 |
| Hh mutants abrogate ligand secretion | 45 | 1.87e-01 | -0.114000 | 6.82e-01 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 60 | 1.28e-01 | -0.114000 | 6.43e-01 |
| Ca-dependent events | 33 | 2.59e-01 | 0.114000 | 7.11e-01 |
| G beta:gamma signalling through CDC42 | 15 | 4.47e-01 | 0.113000 | 8.13e-01 |
| CS/DS degradation | 14 | 4.64e-01 | 0.113000 | 8.25e-01 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 18 | 4.06e-01 | 0.113000 | 7.88e-01 |
| mRNA 3'-end processing | 42 | 2.06e-01 | 0.113000 | 6.87e-01 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | 15 | 4.51e-01 | -0.112000 | 8.16e-01 |
| HDR through Homologous Recombination (HRR) | 53 | 1.57e-01 | -0.112000 | 6.75e-01 |
| Post NMDA receptor activation events | 59 | 1.36e-01 | 0.112000 | 6.62e-01 |
| Cell surface interactions at the vascular wall | 131 | 2.67e-02 | -0.112000 | 4.21e-01 |
| Glycogen synthesis | 12 | 5.01e-01 | 0.112000 | 8.51e-01 |
| Regulation of TP53 Activity through Phosphorylation | 79 | 8.58e-02 | -0.112000 | 6.23e-01 |
| PERK regulates gene expression | 26 | 3.24e-01 | 0.112000 | 7.49e-01 |
| MHC class II antigen presentation | 95 | 6.16e-02 | -0.111000 | 5.61e-01 |
| Organic anion transporters | 10 | 5.44e-01 | -0.111000 | 8.70e-01 |
| Growth hormone receptor signaling | 21 | 3.80e-01 | -0.111000 | 7.82e-01 |
| Visual phototransduction | 88 | 7.31e-02 | -0.111000 | 5.98e-01 |
| Keratan sulfate/keratin metabolism | 28 | 3.12e-01 | -0.110000 | 7.39e-01 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 15 | 4.60e-01 | -0.110000 | 8.24e-01 |
| Beta-catenin phosphorylation cascade | 16 | 4.48e-01 | 0.110000 | 8.13e-01 |
| Keratan sulfate biosynthesis | 24 | 3.53e-01 | -0.110000 | 7.68e-01 |
| mTORC1-mediated signalling | 20 | 3.97e-01 | 0.109000 | 7.85e-01 |
| Heme degradation | 15 | 4.64e-01 | 0.109000 | 8.25e-01 |
| ABC transporter disorders | 60 | 1.45e-01 | -0.109000 | 6.70e-01 |
| Peptide hormone metabolism | 77 | 9.95e-02 | 0.109000 | 6.34e-01 |
| Cytochrome P450 - arranged by substrate type | 56 | 1.60e-01 | 0.109000 | 6.75e-01 |
| Ribosomal scanning and start codon recognition | 32 | 2.89e-01 | 0.108000 | 7.27e-01 |
| TBC/RABGAPs | 37 | 2.55e-01 | -0.108000 | 7.11e-01 |
| Defective B4GALT7 causes EDS, progeroid type | 19 | 4.15e-01 | 0.108000 | 7.94e-01 |
| Chemokine receptors bind chemokines | 47 | 2.01e-01 | 0.108000 | 6.82e-01 |
| Oncogene Induced Senescence | 29 | 3.15e-01 | 0.108000 | 7.39e-01 |
| Misspliced GSK3beta mutants stabilize beta-catenin | 14 | 4.85e-01 | 0.108000 | 8.42e-01 |
| S33 mutants of beta-catenin aren't phosphorylated | 14 | 4.85e-01 | 0.108000 | 8.42e-01 |
| S37 mutants of beta-catenin aren't phosphorylated | 14 | 4.85e-01 | 0.108000 | 8.42e-01 |
| S45 mutants of beta-catenin aren't phosphorylated | 14 | 4.85e-01 | 0.108000 | 8.42e-01 |
| T41 mutants of beta-catenin aren't phosphorylated | 14 | 4.85e-01 | 0.108000 | 8.42e-01 |
| phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex | 14 | 4.85e-01 | 0.108000 | 8.42e-01 |
| RUNX3 regulates NOTCH signaling | 13 | 5.02e-01 | 0.108000 | 8.51e-01 |
| p53-Dependent G1 DNA Damage Response | 53 | 1.76e-01 | -0.107000 | 6.82e-01 |
| p53-Dependent G1/S DNA damage checkpoint | 53 | 1.76e-01 | -0.107000 | 6.82e-01 |
| Degradation of DVL | 46 | 2.09e-01 | -0.107000 | 6.87e-01 |
| LDL clearance | 19 | 4.20e-01 | -0.107000 | 7.95e-01 |
| Formation of the Early Elongation Complex | 25 | 3.55e-01 | -0.107000 | 7.68e-01 |
| Formation of the HIV-1 Early Elongation Complex | 25 | 3.55e-01 | -0.107000 | 7.68e-01 |
| Vpu mediated degradation of CD4 | 41 | 2.38e-01 | -0.106000 | 7.09e-01 |
| NOD1/2 Signaling Pathway | 28 | 3.29e-01 | 0.106000 | 7.52e-01 |
| ABC-family proteins mediated transport | 81 | 9.88e-02 | -0.106000 | 6.34e-01 |
| Regulation of TP53 Degradation | 31 | 3.07e-01 | -0.106000 | 7.39e-01 |
| Long-term potentiation | 22 | 3.90e-01 | 0.106000 | 7.84e-01 |
| Activated point mutants of FGFR2 | 17 | 4.51e-01 | 0.106000 | 8.16e-01 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 14 | 4.95e-01 | -0.105000 | 8.49e-01 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 13 | 5.12e-01 | -0.105000 | 8.57e-01 |
| Constitutive Signaling by Overexpressed ERBB2 | 10 | 5.65e-01 | 0.105000 | 8.73e-01 |
| Mitochondrial protein import | 50 | 2.00e-01 | -0.105000 | 6.82e-01 |
| Recognition of DNA damage by PCNA-containing replication complex | 22 | 3.97e-01 | -0.104000 | 7.85e-01 |
| DNA Double-Strand Break Repair | 108 | 6.12e-02 | -0.104000 | 5.61e-01 |
| Intrinsic Pathway of Fibrin Clot Formation | 21 | 4.09e-01 | -0.104000 | 7.90e-01 |
| SLC-mediated transmembrane transport | 227 | 6.95e-03 | -0.104000 | 3.74e-01 |
| TP53 Regulates Transcription of DNA Repair Genes | 48 | 2.12e-01 | -0.104000 | 6.93e-01 |
| Pre-NOTCH Transcription and Translation | 33 | 3.01e-01 | -0.104000 | 7.34e-01 |
| Regulation of MECP2 expression and activity | 26 | 3.59e-01 | 0.104000 | 7.70e-01 |
| Regulation of FZD by ubiquitination | 17 | 4.60e-01 | 0.104000 | 8.24e-01 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | 63 | 1.56e-01 | -0.103000 | 6.75e-01 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 63 | 1.56e-01 | -0.103000 | 6.75e-01 |
| FGFR3 mutant receptor activation | 12 | 5.35e-01 | 0.103000 | 8.70e-01 |
| Signaling by activated point mutants of FGFR3 | 12 | 5.35e-01 | 0.103000 | 8.70e-01 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 32 | 3.12e-01 | 0.103000 | 7.39e-01 |
| Peroxisomal protein import | 54 | 1.89e-01 | -0.103000 | 6.82e-01 |
| Translation initiation complex formation | 31 | 3.20e-01 | 0.103000 | 7.45e-01 |
| RNA Polymerase III Chain Elongation | 13 | 5.19e-01 | -0.103000 | 8.61e-01 |
| Vif-mediated degradation of APOBEC3G | 40 | 2.60e-01 | -0.103000 | 7.11e-01 |
| Homology Directed Repair | 85 | 1.01e-01 | -0.103000 | 6.34e-01 |
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 24 | 3.84e-01 | -0.103000 | 7.82e-01 |
| Neurotransmitter receptors and postsynaptic signal transmission | 169 | 2.16e-02 | 0.103000 | 4.21e-01 |
| Interleukin-2 family signaling | 40 | 2.63e-01 | -0.102000 | 7.16e-01 |
| Diseases of glycosylation | 127 | 4.69e-02 | -0.102000 | 5.01e-01 |
| Activation of BAD and translocation to mitochondria | 14 | 5.08e-01 | 0.102000 | 8.57e-01 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 12 | 5.40e-01 | -0.102000 | 8.70e-01 |
| Highly calcium permeable postsynaptic nicotinic acetylcholine receptors | 11 | 5.57e-01 | 0.102000 | 8.70e-01 |
| EPHB-mediated forward signaling | 32 | 3.18e-01 | 0.102000 | 7.43e-01 |
| Signaling by Hippo | 19 | 4.42e-01 | 0.102000 | 8.13e-01 |
| Prefoldin mediated transfer of substrate to CCT/TriC | 23 | 3.98e-01 | -0.102000 | 7.86e-01 |
| TRAF3-dependent IRF activation pathway | 14 | 5.11e-01 | -0.102000 | 8.57e-01 |
| Regulation of ornithine decarboxylase (ODC) | 43 | 2.50e-01 | -0.102000 | 7.11e-01 |
| Reversible hydration of carbon dioxide | 12 | 5.43e-01 | 0.101000 | 8.70e-01 |
| Regulation of HSF1-mediated heat shock response | 58 | 1.82e-01 | 0.101000 | 6.82e-01 |
| Metabolism of non-coding RNA | 39 | 2.73e-01 | 0.101000 | 7.27e-01 |
| snRNP Assembly | 39 | 2.73e-01 | 0.101000 | 7.27e-01 |
| Formation of the cornified envelope | 43 | 2.52e-01 | 0.101000 | 7.11e-01 |
| Degradation of AXIN | 43 | 2.52e-01 | -0.101000 | 7.11e-01 |
| Signaling by TGFB family members | 87 | 1.04e-01 | 0.101000 | 6.34e-01 |
| Signalling to ERKs | 34 | 3.10e-01 | 0.101000 | 7.39e-01 |
| Telomere Maintenance | 52 | 2.10e-01 | -0.101000 | 6.87e-01 |
| CDK-mediated phosphorylation and removal of Cdc6 | 60 | 1.78e-01 | -0.100000 | 6.82e-01 |
| Negative regulators of DDX58/IFIH1 signaling | 25 | 3.85e-01 | -0.100000 | 7.82e-01 |
| Activation of the TFAP2 (AP-2) family of transcription factors | 11 | 5.65e-01 | 0.100000 | 8.73e-01 |
| Phosphorylation of the APC/C | 17 | 4.75e-01 | -0.100000 | 8.35e-01 |
| Negative regulation of NOTCH4 signaling | 43 | 2.59e-01 | -0.099500 | 7.11e-01 |
| Interleukin-17 signaling | 64 | 1.71e-01 | 0.098900 | 6.82e-01 |
| Inositol phosphate metabolism | 45 | 2.51e-01 | -0.098900 | 7.11e-01 |
| Free fatty acids regulate insulin secretion | 11 | 5.70e-01 | -0.098900 | 8.78e-01 |
| Regulation of Apoptosis | 41 | 2.77e-01 | -0.098200 | 7.27e-01 |
| Metabolism of Angiotensinogen to Angiotensins | 16 | 4.98e-01 | 0.097900 | 8.49e-01 |
| Regulation of TP53 Activity through Association with Co-factors | 14 | 5.26e-01 | -0.097800 | 8.66e-01 |
| TGF-beta receptor signaling activates SMADs | 23 | 4.19e-01 | 0.097500 | 7.95e-01 |
| Glutathione conjugation | 30 | 3.57e-01 | -0.097200 | 7.68e-01 |
| Molecules associated with elastic fibres | 29 | 3.65e-01 | -0.097200 | 7.74e-01 |
| Translesion synthesis by POLK | 13 | 5.45e-01 | -0.097000 | 8.70e-01 |
| Negative regulation of FGFR4 signaling | 27 | 3.84e-01 | 0.096800 | 7.82e-01 |
| Biological oxidations | 183 | 2.47e-02 | 0.096400 | 4.21e-01 |
| Hedgehog ligand biogenesis | 51 | 2.34e-01 | -0.096400 | 7.09e-01 |
| Diseases of metabolism | 212 | 1.58e-02 | -0.096300 | 4.21e-01 |
| Dissolution of Fibrin Clot | 13 | 5.49e-01 | 0.096100 | 8.70e-01 |
| Negative regulation of FGFR1 signaling | 29 | 3.71e-01 | 0.096100 | 7.82e-01 |
| Stimuli-sensing channels | 89 | 1.18e-01 | 0.096000 | 6.34e-01 |
| TP53 Regulates Transcription of Cell Death Genes | 36 | 3.19e-01 | 0.095900 | 7.45e-01 |
| Transport of inorganic cations/anions and amino acids/oligopeptides | 101 | 9.61e-02 | -0.095900 | 6.34e-01 |
| p130Cas linkage to MAPK signaling for integrins | 15 | 5.20e-01 | -0.095900 | 8.61e-01 |
| DNA Damage Bypass | 35 | 3.27e-01 | -0.095700 | 7.50e-01 |
| Phospholipid metabolism | 183 | 2.59e-02 | -0.095600 | 4.21e-01 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 50 | 2.43e-01 | -0.095500 | 7.09e-01 |
| Thromboxane signalling through TP receptor | 18 | 4.83e-01 | -0.095500 | 8.42e-01 |
| Integration of energy metabolism | 100 | 1.01e-01 | -0.095000 | 6.34e-01 |
| RHO GTPases activate IQGAPs | 11 | 5.86e-01 | 0.094900 | 8.84e-01 |
| PECAM1 interactions | 11 | 5.86e-01 | -0.094800 | 8.84e-01 |
| CDT1 association with the CDC6:ORC:origin complex | 46 | 2.66e-01 | -0.094800 | 7.17e-01 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 27 | 3.94e-01 | 0.094800 | 7.84e-01 |
| Metabolism of fat-soluble vitamins | 39 | 3.06e-01 | -0.094800 | 7.39e-01 |
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 40 | 3.00e-01 | -0.094600 | 7.34e-01 |
| p53-Independent DNA Damage Response | 40 | 3.00e-01 | -0.094600 | 7.34e-01 |
| p53-Independent G1/S DNA damage checkpoint | 40 | 3.00e-01 | -0.094600 | 7.34e-01 |
| Ubiquitin-dependent degradation of Cyclin D | 41 | 2.95e-01 | -0.094600 | 7.32e-01 |
| AMER1 mutants destabilize the destruction complex | 13 | 5.55e-01 | 0.094600 | 8.70e-01 |
| APC truncation mutants have impaired AXIN binding | 13 | 5.55e-01 | 0.094600 | 8.70e-01 |
| AXIN missense mutants destabilize the destruction complex | 13 | 5.55e-01 | 0.094600 | 8.70e-01 |
| AXIN mutants destabilize the destruction complex, activating WNT signaling | 13 | 5.55e-01 | 0.094600 | 8.70e-01 |
| Truncations of AMER1 destabilize the destruction complex | 13 | 5.55e-01 | 0.094600 | 8.70e-01 |
| truncated APC mutants destabilize the destruction complex | 13 | 5.55e-01 | 0.094600 | 8.70e-01 |
| The role of Nef in HIV-1 replication and disease pathogenesis | 26 | 4.05e-01 | -0.094400 | 7.88e-01 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 36 | 3.27e-01 | -0.094400 | 7.50e-01 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 67 | 1.83e-01 | 0.094200 | 6.82e-01 |
| Nonsense-Mediated Decay (NMD) | 67 | 1.83e-01 | 0.094200 | 6.82e-01 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 78 | 1.51e-01 | 0.094100 | 6.74e-01 |
| Formation of the ternary complex, and subsequently, the 43S complex | 28 | 3.89e-01 | 0.094000 | 7.84e-01 |
| Heparan sulfate/heparin (HS-GAG) metabolism | 48 | 2.60e-01 | 0.094000 | 7.11e-01 |
| Insulin receptor recycling | 23 | 4.36e-01 | 0.093900 | 8.08e-01 |
| Circadian Clock | 62 | 2.02e-01 | 0.093800 | 6.83e-01 |
| FGFR2c ligand binding and activation | 13 | 5.58e-01 | 0.093800 | 8.70e-01 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 60 | 2.10e-01 | -0.093600 | 6.87e-01 |
| Glycolysis | 59 | 2.15e-01 | -0.093400 | 6.93e-01 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 61 | 2.08e-01 | -0.093200 | 6.87e-01 |
| UCH proteinases | 69 | 1.81e-01 | -0.093100 | 6.82e-01 |
| P2Y receptors | 10 | 6.11e-01 | 0.093000 | 8.98e-01 |
| Synthesis of bile acids and bile salts | 28 | 3.95e-01 | -0.092900 | 7.84e-01 |
| Role of phospholipids in phagocytosis | 30 | 3.79e-01 | -0.092900 | 7.82e-01 |
| Regulation of TNFR1 signaling | 26 | 4.12e-01 | -0.092900 | 7.92e-01 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 27 | 4.04e-01 | -0.092900 | 7.88e-01 |
| O-linked glycosylation of mucins | 54 | 2.38e-01 | -0.092800 | 7.09e-01 |
| FOXO-mediated transcription | 60 | 2.14e-01 | 0.092800 | 6.93e-01 |
| Disorders of transmembrane transporters | 146 | 5.33e-02 | -0.092800 | 5.31e-01 |
| Signaling by FGFR1 in disease | 37 | 3.31e-01 | 0.092400 | 7.52e-01 |
| GAB1 signalosome | 17 | 5.10e-01 | 0.092200 | 8.57e-01 |
| Response of EIF2AK1 (HRI) to heme deficiency | 12 | 5.80e-01 | 0.092200 | 8.83e-01 |
| Inwardly rectifying K+ channels | 30 | 3.83e-01 | -0.092100 | 7.82e-01 |
| DNA Replication Pre-Initiation | 68 | 1.89e-01 | -0.092100 | 6.82e-01 |
| TNFR1-induced proapoptotic signaling | 13 | 5.66e-01 | -0.092000 | 8.74e-01 |
| Presynaptic depolarization and calcium channel opening | 12 | 5.81e-01 | -0.091900 | 8.83e-01 |
| TP53 Regulates Transcription of Cell Cycle Genes | 46 | 2.81e-01 | -0.091800 | 7.27e-01 |
| MyD88 dependent cascade initiated on endosome | 79 | 1.59e-01 | 0.091700 | 6.75e-01 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 79 | 1.59e-01 | 0.091700 | 6.75e-01 |
| Regulation of PTEN gene transcription | 55 | 2.41e-01 | -0.091500 | 7.09e-01 |
| Metabolism of polyamines | 50 | 2.65e-01 | -0.091200 | 7.16e-01 |
| Nucleotide-like (purinergic) receptors | 13 | 5.70e-01 | 0.091100 | 8.78e-01 |
| Miscellaneous transport and binding events | 22 | 4.61e-01 | 0.090800 | 8.24e-01 |
| The phototransduction cascade | 30 | 3.90e-01 | -0.090700 | 7.84e-01 |
| Ovarian tumor domain proteases | 30 | 3.90e-01 | 0.090600 | 7.84e-01 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 24 | 4.42e-01 | -0.090600 | 8.13e-01 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 44 | 2.99e-01 | -0.090500 | 7.34e-01 |
| tRNA processing | 84 | 1.57e-01 | -0.089300 | 6.75e-01 |
| Retinoid metabolism and transport | 37 | 3.49e-01 | -0.089000 | 7.68e-01 |
| activated TAK1 mediates p38 MAPK activation | 17 | 5.26e-01 | 0.088800 | 8.66e-01 |
| Presynaptic nicotinic acetylcholine receptors | 12 | 5.95e-01 | -0.088600 | 8.90e-01 |
| Metabolism of steroids | 130 | 8.28e-02 | -0.088200 | 6.20e-01 |
| Toll Like Receptor 9 (TLR9) Cascade | 82 | 1.69e-01 | 0.088000 | 6.82e-01 |
| Metabolism of nucleotides | 87 | 1.57e-01 | -0.087900 | 6.75e-01 |
| Cargo concentration in the ER | 25 | 4.47e-01 | -0.087900 | 8.13e-01 |
| G1/S DNA Damage Checkpoints | 55 | 2.61e-01 | -0.087600 | 7.13e-01 |
| SCF-beta-TrCP mediated degradation of Emi1 | 44 | 3.15e-01 | -0.087500 | 7.39e-01 |
| Cytosolic sensors of pathogen-associated DNA | 49 | 2.90e-01 | -0.087400 | 7.27e-01 |
| Asparagine N-linked glycosylation | 239 | 2.03e-02 | -0.087300 | 4.21e-01 |
| Beta-catenin independent WNT signaling | 125 | 9.25e-02 | -0.087200 | 6.34e-01 |
| Mitochondrial biogenesis | 67 | 2.18e-01 | -0.087200 | 6.93e-01 |
| Formation of tubulin folding intermediates by CCT/TriC | 21 | 4.90e-01 | -0.087100 | 8.44e-01 |
| Diseases associated with N-glycosylation of proteins | 16 | 5.47e-01 | -0.087100 | 8.70e-01 |
| Extracellular matrix organization | 268 | 1.45e-02 | -0.086900 | 4.21e-01 |
| Phase I - Functionalization of compounds | 92 | 1.50e-01 | 0.086800 | 6.74e-01 |
| RIP-mediated NFkB activation via ZBP1 | 15 | 5.63e-01 | -0.086300 | 8.72e-01 |
| Metabolism of water-soluble vitamins and cofactors | 99 | 1.38e-01 | -0.086300 | 6.65e-01 |
| Translesion Synthesis by POLH | 12 | 6.06e-01 | -0.085900 | 8.96e-01 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 43 | 3.32e-01 | -0.085500 | 7.52e-01 |
| Metabolism of carbohydrates | 252 | 1.97e-02 | -0.085500 | 4.21e-01 |
| Factors involved in megakaryocyte development and platelet production | 119 | 1.08e-01 | 0.085400 | 6.34e-01 |
| PRC2 methylates histones and DNA | 12 | 6.09e-01 | 0.085300 | 8.96e-01 |
| BBSome-mediated cargo-targeting to cilium | 19 | 5.20e-01 | 0.085300 | 8.61e-01 |
| Rho GTPase cycle | 131 | 9.31e-02 | -0.085000 | 6.34e-01 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 30 | 4.21e-01 | 0.084900 | 7.95e-01 |
| Tandem pore domain potassium channels | 11 | 6.27e-01 | 0.084700 | 9.04e-01 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | 14 | 5.84e-01 | 0.084600 | 8.84e-01 |
| Inactivation, recovery and regulation of the phototransduction cascade | 29 | 4.31e-01 | -0.084500 | 8.04e-01 |
| Metabolism of nitric oxide: NOS3 activation and regulation | 14 | 5.85e-01 | -0.084200 | 8.84e-01 |
| Assembly of the pre-replicative complex | 54 | 2.85e-01 | -0.084200 | 7.27e-01 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 49 | 3.12e-01 | 0.083500 | 7.39e-01 |
| Interleukin-12 signaling | 38 | 3.73e-01 | 0.083500 | 7.82e-01 |
| Gene Silencing by RNA | 56 | 2.80e-01 | -0.083500 | 7.27e-01 |
| Degradation of the extracellular matrix | 100 | 1.50e-01 | -0.083400 | 6.74e-01 |
| NS1 Mediated Effects on Host Pathways | 29 | 4.39e-01 | 0.083100 | 8.10e-01 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 20 | 5.20e-01 | -0.083100 | 8.61e-01 |
| Defective CFTR causes cystic fibrosis | 46 | 3.32e-01 | -0.082800 | 7.52e-01 |
| MAPK6/MAPK4 signaling | 75 | 2.16e-01 | -0.082700 | 6.93e-01 |
| Fatty acid metabolism | 148 | 8.29e-02 | -0.082700 | 6.20e-01 |
| Metabolism of vitamins and cofactors | 156 | 7.51e-02 | -0.082700 | 5.99e-01 |
| Regulation of TP53 Expression and Degradation | 32 | 4.19e-01 | -0.082500 | 7.95e-01 |
| Phosphorylation of CD3 and TCR zeta chains | 15 | 5.81e-01 | -0.082300 | 8.83e-01 |
| PLC beta mediated events | 49 | 3.21e-01 | 0.082000 | 7.46e-01 |
| Signaling by ERBB2 | 43 | 3.53e-01 | 0.081900 | 7.68e-01 |
| Homologous DNA Pairing and Strand Exchange | 36 | 3.95e-01 | -0.081900 | 7.84e-01 |
| Extension of Telomeres | 43 | 3.53e-01 | -0.081800 | 7.68e-01 |
| Interleukin-37 signaling | 19 | 5.38e-01 | -0.081700 | 8.70e-01 |
| Binding and Uptake of Ligands by Scavenger Receptors | 40 | 3.72e-01 | -0.081600 | 7.82e-01 |
| Transport of Ribonucleoproteins into the Host Nucleus | 23 | 4.98e-01 | 0.081600 | 8.49e-01 |
| Mitochondrial translation elongation | 64 | 2.60e-01 | -0.081500 | 7.11e-01 |
| Mitochondrial translation | 70 | 2.41e-01 | -0.081100 | 7.09e-01 |
| Golgi-to-ER retrograde transport | 104 | 1.54e-01 | -0.081000 | 6.75e-01 |
| SLC transporter disorders | 86 | 1.96e-01 | -0.080800 | 6.82e-01 |
| DNA Replication | 107 | 1.51e-01 | -0.080500 | 6.74e-01 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 19 | 5.44e-01 | -0.080400 | 8.70e-01 |
| Transcriptional regulation by RUNX2 | 104 | 1.57e-01 | 0.080300 | 6.75e-01 |
| Regulation of lipid metabolism by PPARalpha | 110 | 1.46e-01 | 0.080300 | 6.70e-01 |
| Antigen processing-Cross presentation | 77 | 2.24e-01 | -0.080300 | 6.94e-01 |
| RET signaling | 38 | 3.92e-01 | -0.080200 | 7.84e-01 |
| ADP signalling through P2Y purinoceptor 1 | 20 | 5.35e-01 | -0.080100 | 8.70e-01 |
| Caspase-mediated cleavage of cytoskeletal proteins | 11 | 6.46e-01 | -0.080100 | 9.17e-01 |
| Constitutive Signaling by AKT1 E17K in Cancer | 24 | 4.99e-01 | -0.079800 | 8.49e-01 |
| APC/C-mediated degradation of cell cycle proteins | 74 | 2.37e-01 | -0.079600 | 7.09e-01 |
| Regulation of mitotic cell cycle | 74 | 2.37e-01 | -0.079600 | 7.09e-01 |
| Deposition of new CENPA-containing nucleosomes at the centromere | 19 | 5.49e-01 | 0.079500 | 8.70e-01 |
| Nucleosome assembly | 19 | 5.49e-01 | 0.079500 | 8.70e-01 |
| Signaling by NTRK3 (TRKC) | 17 | 5.70e-01 | 0.079500 | 8.78e-01 |
| NOTCH1 Intracellular Domain Regulates Transcription | 41 | 3.79e-01 | 0.079400 | 7.82e-01 |
| DNA Repair | 225 | 4.17e-02 | -0.078900 | 5.01e-01 |
| O-linked glycosylation | 93 | 1.89e-01 | -0.078900 | 6.82e-01 |
| SUMOylation of transcription cofactors | 36 | 4.15e-01 | -0.078600 | 7.94e-01 |
| PPARA activates gene expression | 108 | 1.59e-01 | 0.078400 | 6.75e-01 |
| Nuclear Envelope (NE) Reassembly | 63 | 2.83e-01 | -0.078200 | 7.27e-01 |
| HS-GAG degradation | 19 | 5.57e-01 | -0.077900 | 8.70e-01 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 14 | 6.14e-01 | -0.077900 | 8.99e-01 |
| tRNA Aminoacylation | 20 | 5.48e-01 | -0.077700 | 8.70e-01 |
| Signaling by NOTCH2 | 23 | 5.20e-01 | 0.077600 | 8.61e-01 |
| G beta:gamma signalling through PI3Kgamma | 19 | 5.59e-01 | -0.077500 | 8.70e-01 |
| N-glycan antennae elongation in the medial/trans-Golgi | 23 | 5.20e-01 | -0.077500 | 8.61e-01 |
| EPH-ephrin mediated repulsion of cells | 43 | 3.81e-01 | -0.077300 | 7.82e-01 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 53 | 3.31e-01 | 0.077100 | 7.52e-01 |
| Signal Transduction | 2361 | 1.98e-09 | 0.077000 | 5.50e-07 |
| Synthesis of DNA | 100 | 1.84e-01 | -0.077000 | 6.82e-01 |
| Digestion | 20 | 5.53e-01 | 0.076600 | 8.70e-01 |
| FRS-mediated FGFR1 signaling | 22 | 5.35e-01 | 0.076400 | 8.70e-01 |
| Deadenylation-dependent mRNA decay | 45 | 3.77e-01 | 0.076200 | 7.82e-01 |
| G-protein mediated events | 50 | 3.52e-01 | 0.076100 | 7.68e-01 |
| Signaling by NOTCH | 154 | 1.05e-01 | -0.075800 | 6.34e-01 |
| G0 and Early G1 | 25 | 5.13e-01 | -0.075500 | 8.57e-01 |
| CYP2E1 reactions | 11 | 6.65e-01 | 0.075500 | 9.25e-01 |
| FRS-mediated FGFR4 signaling | 20 | 5.59e-01 | 0.075400 | 8.70e-01 |
| Assembly of collagen fibrils and other multimeric structures | 53 | 3.43e-01 | -0.075400 | 7.61e-01 |
| SHC-mediated cascade:FGFR1 | 21 | 5.50e-01 | 0.075400 | 8.70e-01 |
| Vitamin B5 (pantothenate) metabolism | 14 | 6.27e-01 | -0.075100 | 9.04e-01 |
| mRNA Splicing - Minor Pathway | 37 | 4.30e-01 | -0.074900 | 8.04e-01 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 82 | 2.42e-01 | 0.074700 | 7.09e-01 |
| Toll Like Receptor 2 (TLR2) Cascade | 82 | 2.42e-01 | 0.074700 | 7.09e-01 |
| Toll Like Receptor TLR1:TLR2 Cascade | 82 | 2.42e-01 | 0.074700 | 7.09e-01 |
| Toll Like Receptor TLR6:TLR2 Cascade | 82 | 2.42e-01 | 0.074700 | 7.09e-01 |
| Glucagon-type ligand receptors | 28 | 4.97e-01 | -0.074200 | 8.49e-01 |
| SHC-mediated cascade:FGFR4 | 19 | 5.76e-01 | 0.074200 | 8.81e-01 |
| DAG and IP3 signaling | 37 | 4.35e-01 | 0.074200 | 8.08e-01 |
| Protein localization | 132 | 1.43e-01 | -0.073900 | 6.70e-01 |
| Ion homeostasis | 48 | 3.76e-01 | 0.073800 | 7.82e-01 |
| Transcriptional activation of mitochondrial biogenesis | 49 | 3.72e-01 | -0.073700 | 7.82e-01 |
| Activation of HOX genes during differentiation | 45 | 3.94e-01 | 0.073500 | 7.84e-01 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 45 | 3.94e-01 | 0.073500 | 7.84e-01 |
| Interleukin-15 signaling | 13 | 6.46e-01 | -0.073500 | 9.18e-01 |
| Intra-Golgi traffic | 36 | 4.48e-01 | 0.073100 | 8.13e-01 |
| Uptake and function of anthrax toxins | 11 | 6.78e-01 | -0.072300 | 9.31e-01 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 25 | 5.32e-01 | -0.072200 | 8.70e-01 |
| Epigenetic regulation of gene expression | 72 | 2.91e-01 | -0.072000 | 7.27e-01 |
| Nuclear Pore Complex (NPC) Disassembly | 27 | 5.17e-01 | 0.072000 | 8.61e-01 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 16 | 6.18e-01 | -0.071900 | 9.01e-01 |
| ZBP1(DAI) mediated induction of type I IFNs | 19 | 5.88e-01 | -0.071900 | 8.84e-01 |
| MyD88 cascade initiated on plasma membrane | 71 | 2.96e-01 | 0.071800 | 7.32e-01 |
| Toll Like Receptor 10 (TLR10) Cascade | 71 | 2.96e-01 | 0.071800 | 7.32e-01 |
| Toll Like Receptor 5 (TLR5) Cascade | 71 | 2.96e-01 | 0.071800 | 7.32e-01 |
| MyD88-independent TLR4 cascade | 85 | 2.53e-01 | 0.071700 | 7.11e-01 |
| TRIF(TICAM1)-mediated TLR4 signaling | 85 | 2.53e-01 | 0.071700 | 7.11e-01 |
| Plasma lipoprotein assembly | 15 | 6.31e-01 | -0.071700 | 9.05e-01 |
| Regulation of signaling by CBL | 18 | 6.01e-01 | 0.071300 | 8.91e-01 |
| CaM pathway | 31 | 4.93e-01 | 0.071200 | 8.47e-01 |
| Calmodulin induced events | 31 | 4.93e-01 | 0.071200 | 8.47e-01 |
| Export of Viral Ribonucleoproteins from Nucleus | 24 | 5.47e-01 | 0.071000 | 8.70e-01 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 56 | 3.59e-01 | 0.070900 | 7.70e-01 |
| Keratinization | 116 | 1.88e-01 | -0.070800 | 6.82e-01 |
| Purine salvage | 11 | 6.84e-01 | -0.070800 | 9.31e-01 |
| Neuronal System | 360 | 2.15e-02 | 0.070700 | 4.21e-01 |
| Organic cation transport | 10 | 6.99e-01 | -0.070600 | 9.31e-01 |
| Regulation of IFNG signaling | 13 | 6.59e-01 | -0.070600 | 9.24e-01 |
| NOTCH4 Intracellular Domain Regulates Transcription | 17 | 6.15e-01 | 0.070500 | 8.99e-01 |
| Platelet homeostasis | 78 | 2.82e-01 | -0.070500 | 7.27e-01 |
| Fc epsilon receptor (FCERI) signaling | 119 | 1.85e-01 | 0.070400 | 6.82e-01 |
| Interleukin-7 signaling | 17 | 6.17e-01 | -0.070100 | 8.99e-01 |
| Killing mechanisms | 10 | 7.01e-01 | -0.070000 | 9.31e-01 |
| WNT5:FZD7-mediated leishmania damping | 10 | 7.01e-01 | -0.070000 | 9.31e-01 |
| Fcgamma receptor (FCGR) dependent phagocytosis | 89 | 2.55e-01 | -0.069900 | 7.11e-01 |
| Neutrophil degranulation | 398 | 1.73e-02 | -0.069800 | 4.21e-01 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 11 | 6.89e-01 | -0.069700 | 9.31e-01 |
| Dectin-1 mediated noncanonical NF-kB signaling | 49 | 4.02e-01 | -0.069300 | 7.88e-01 |
| Metabolism | 1736 | 2.50e-06 | -0.069000 | 5.79e-04 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 19 | 6.05e-01 | -0.068600 | 8.95e-01 |
| Signaling by ROBO receptors | 150 | 1.49e-01 | 0.068300 | 6.74e-01 |
| Regulation of APC/C activators between G1/S and early anaphase | 67 | 3.34e-01 | -0.068300 | 7.55e-01 |
| Aggrephagy | 18 | 6.16e-01 | -0.068200 | 8.99e-01 |
| Interactions of Vpr with host cellular proteins | 26 | 5.48e-01 | 0.068100 | 8.70e-01 |
| Sphingolipid metabolism | 74 | 3.11e-01 | -0.068100 | 7.39e-01 |
| Global Genome Nucleotide Excision Repair (GG-NER) | 69 | 3.29e-01 | -0.068000 | 7.52e-01 |
| RNA polymerase II transcribes snRNA genes | 60 | 3.64e-01 | 0.067900 | 7.72e-01 |
| Cell-cell junction organization | 54 | 3.93e-01 | 0.067200 | 7.84e-01 |
| Norepinephrine Neurotransmitter Release Cycle | 15 | 6.53e-01 | -0.067100 | 9.21e-01 |
| Mitochondrial translation termination | 64 | 3.53e-01 | -0.067100 | 7.68e-01 |
| RNA Polymerase I Transcription Termination | 22 | 5.87e-01 | -0.066900 | 8.84e-01 |
| Cytosolic sulfonation of small molecules | 21 | 6.00e-01 | -0.066100 | 8.91e-01 |
| Synthesis of pyrophosphates in the cytosol | 10 | 7.19e-01 | -0.065800 | 9.35e-01 |
| G beta:gamma signalling through PLC beta | 15 | 6.59e-01 | -0.065800 | 9.24e-01 |
| Major pathway of rRNA processing in the nucleolus and cytosol | 119 | 2.15e-01 | -0.065800 | 6.93e-01 |
| Interleukin-6 signaling | 11 | 7.07e-01 | -0.065400 | 9.31e-01 |
| CD28 co-stimulation | 32 | 5.25e-01 | 0.064900 | 8.66e-01 |
| Dual incision in TC-NER | 51 | 4.23e-01 | -0.064800 | 7.97e-01 |
| ER-Phagosome pathway | 62 | 3.79e-01 | -0.064700 | 7.82e-01 |
| Respiratory electron transport | 70 | 3.51e-01 | 0.064500 | 7.68e-01 |
| Protein-protein interactions at synapses | 84 | 3.07e-01 | 0.064500 | 7.39e-01 |
| Transmission across Chemical Synapses | 226 | 9.58e-02 | 0.064400 | 6.34e-01 |
| FCGR activation | 19 | 6.27e-01 | 0.064300 | 9.04e-01 |
| Association of TriC/CCT with target proteins during biosynthesis | 32 | 5.29e-01 | 0.064300 | 8.70e-01 |
| Negative regulation of the PI3K/AKT network | 105 | 2.56e-01 | 0.064200 | 7.11e-01 |
| Mitochondrial translation initiation | 64 | 3.76e-01 | -0.064100 | 7.82e-01 |
| Effects of PIP2 hydrolysis | 25 | 5.80e-01 | -0.064000 | 8.83e-01 |
| Fatty acyl-CoA biosynthesis | 29 | 5.53e-01 | -0.063700 | 8.70e-01 |
| Scavenging of heme from plasma | 14 | 6.81e-01 | 0.063400 | 9.31e-01 |
| Signaling by PDGFRA extracellular domain mutants | 12 | 7.04e-01 | 0.063400 | 9.31e-01 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 12 | 7.04e-01 | 0.063400 | 9.31e-01 |
| ESR-mediated signaling | 148 | 1.85e-01 | 0.063300 | 6.82e-01 |
| Regulation of RUNX2 expression and activity | 60 | 3.98e-01 | 0.063100 | 7.86e-01 |
| Transport of small molecules | 633 | 7.01e-03 | -0.063100 | 3.74e-01 |
| Iron uptake and transport | 49 | 4.48e-01 | 0.062700 | 8.13e-01 |
| TNFs bind their physiological receptors | 26 | 5.80e-01 | -0.062600 | 8.83e-01 |
| RA biosynthesis pathway | 20 | 6.29e-01 | -0.062400 | 9.05e-01 |
| Signaling by WNT in cancer | 30 | 5.55e-01 | 0.062300 | 8.70e-01 |
| Signaling by TGF-beta Receptor Complex | 60 | 4.05e-01 | 0.062200 | 7.88e-01 |
| SCF(Skp2)-mediated degradation of p27/p21 | 49 | 4.52e-01 | -0.062200 | 8.16e-01 |
| RHO GTPases Activate Formins | 100 | 2.84e-01 | 0.062000 | 7.27e-01 |
| Regulation of KIT signaling | 16 | 6.68e-01 | 0.062000 | 9.26e-01 |
| Arachidonic acid metabolism | 50 | 4.52e-01 | -0.061600 | 8.16e-01 |
| Response to elevated platelet cytosolic Ca2+ | 118 | 2.49e-01 | -0.061500 | 7.11e-01 |
| EML4 and NUDC in mitotic spindle formation | 81 | 3.40e-01 | 0.061400 | 7.61e-01 |
| FOXO-mediated transcription of cell cycle genes | 16 | 6.71e-01 | 0.061300 | 9.27e-01 |
| Pentose phosphate pathway | 14 | 6.92e-01 | -0.061100 | 9.31e-01 |
| COPI-independent Golgi-to-ER retrograde traffic | 32 | 5.51e-01 | 0.060900 | 8.70e-01 |
| Branched-chain amino acid catabolism | 19 | 6.50e-01 | -0.060100 | 9.21e-01 |
| TNFR2 non-canonical NF-kB pathway | 83 | 3.45e-01 | -0.060000 | 7.62e-01 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) | 34 | 5.49e-01 | 0.059400 | 8.70e-01 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | 10 | 7.45e-01 | -0.059400 | 9.49e-01 |
| RNA Polymerase I Promoter Escape | 22 | 6.30e-01 | -0.059400 | 9.05e-01 |
| Toll Like Receptor 3 (TLR3) Cascade | 81 | 3.56e-01 | 0.059300 | 7.68e-01 |
| HCMV Late Events | 41 | 5.12e-01 | -0.059200 | 8.57e-01 |
| Resolution of Sister Chromatid Cohesion | 89 | 3.37e-01 | 0.058900 | 7.61e-01 |
| Neurotransmitter release cycle | 44 | 5.01e-01 | 0.058700 | 8.51e-01 |
| rRNA processing in the nucleus and cytosol | 126 | 2.56e-01 | -0.058600 | 7.11e-01 |
| rRNA processing | 133 | 2.45e-01 | -0.058400 | 7.11e-01 |
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 76 | 3.80e-01 | 0.058300 | 7.82e-01 |
| Transcriptional Regulation by VENTX | 35 | 5.52e-01 | -0.058100 | 8.70e-01 |
| G1/S-Specific Transcription | 26 | 6.09e-01 | -0.058000 | 8.96e-01 |
| Signaling by NOTCH4 | 66 | 4.16e-01 | -0.057900 | 7.95e-01 |
| Host Interactions of HIV factors | 102 | 3.13e-01 | -0.057900 | 7.39e-01 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 28 | 5.97e-01 | 0.057800 | 8.90e-01 |
| O-glycosylation of TSR domain-containing proteins | 35 | 5.58e-01 | -0.057300 | 8.70e-01 |
| Death Receptor Signalling | 122 | 2.75e-01 | -0.057300 | 7.27e-01 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 19 | 6.67e-01 | -0.057000 | 9.26e-01 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 33 | 5.72e-01 | 0.056800 | 8.78e-01 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | 19 | 6.69e-01 | -0.056600 | 9.26e-01 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 19 | 6.69e-01 | -0.056600 | 9.26e-01 |
| Antigen processing: Ubiquitination & Proteasome degradation | 262 | 1.16e-01 | 0.056600 | 6.34e-01 |
| Transcriptional Regulation by TP53 | 307 | 8.97e-02 | -0.056400 | 6.23e-01 |
| RHO GTPases activate KTN1 | 10 | 7.59e-01 | -0.056100 | 9.54e-01 |
| Physiological factors | 12 | 7.39e-01 | 0.055600 | 9.44e-01 |
| Regulation of PTEN stability and activity | 54 | 4.82e-01 | -0.055400 | 8.42e-01 |
| PI-3K cascade:FGFR1 | 21 | 6.61e-01 | 0.055400 | 9.24e-01 |
| Formation of Incision Complex in GG-NER | 33 | 5.83e-01 | -0.055300 | 8.84e-01 |
| Chylomicron remodeling | 10 | 7.62e-01 | -0.055300 | 9.54e-01 |
| Transcriptional regulation by RUNX1 | 161 | 2.29e-01 | -0.055000 | 6.98e-01 |
| Defective B3GALTL causes Peters-plus syndrome (PpS) | 34 | 5.79e-01 | -0.055000 | 8.83e-01 |
| Collagen formation | 81 | 3.93e-01 | -0.055000 | 7.84e-01 |
| ABC transporters in lipid homeostasis | 14 | 7.23e-01 | -0.054700 | 9.36e-01 |
| ER Quality Control Compartment (ERQC) | 14 | 7.24e-01 | -0.054600 | 9.36e-01 |
| Metabolism of lipids | 631 | 2.03e-02 | -0.054400 | 4.21e-01 |
| Glycogen metabolism | 23 | 6.52e-01 | -0.054300 | 9.21e-01 |
| A tetrasaccharide linker sequence is required for GAG synthesis | 25 | 6.39e-01 | 0.054200 | 9.14e-01 |
| Transport of bile salts and organic acids, metal ions and amine compounds | 75 | 4.18e-01 | -0.054200 | 7.95e-01 |
| NEP/NS2 Interacts with the Cellular Export Machinery | 23 | 6.55e-01 | 0.053900 | 9.22e-01 |
| PTEN Regulation | 123 | 3.04e-01 | -0.053700 | 7.39e-01 |
| Centrosome maturation | 70 | 4.38e-01 | -0.053600 | 8.10e-01 |
| Recruitment of mitotic centrosome proteins and complexes | 70 | 4.38e-01 | -0.053600 | 8.10e-01 |
| Chondroitin sulfate/dermatan sulfate metabolism | 49 | 5.17e-01 | 0.053600 | 8.61e-01 |
| Chromosome Maintenance | 69 | 4.46e-01 | -0.053100 | 8.13e-01 |
| Complement cascade | 55 | 4.98e-01 | -0.052900 | 8.49e-01 |
| Collagen degradation | 36 | 5.85e-01 | -0.052600 | 8.84e-01 |
| Nuclear signaling by ERBB4 | 30 | 6.19e-01 | 0.052500 | 9.01e-01 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants | 11 | 7.64e-01 | -0.052200 | 9.55e-01 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer | 11 | 7.64e-01 | -0.052200 | 9.55e-01 |
| Peptide hormone biosynthesis | 10 | 7.75e-01 | 0.052200 | 9.58e-01 |
| Senescence-Associated Secretory Phenotype (SASP) | 44 | 5.50e-01 | -0.052200 | 8.70e-01 |
| Glycogen breakdown (glycogenolysis) | 14 | 7.36e-01 | -0.052100 | 9.41e-01 |
| PI-3K cascade:FGFR4 | 19 | 6.94e-01 | 0.052100 | 9.31e-01 |
| Opioid Signalling | 79 | 4.24e-01 | 0.052100 | 7.97e-01 |
| Phase 0 - rapid depolarisation | 39 | 5.75e-01 | -0.051900 | 8.81e-01 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | 73 | 4.46e-01 | -0.051600 | 8.13e-01 |
| Post-translational protein phosphorylation | 98 | 3.77e-01 | 0.051600 | 7.82e-01 |
| MET activates PTK2 signaling | 18 | 7.06e-01 | -0.051400 | 9.31e-01 |
| Signaling by KIT in disease | 20 | 6.92e-01 | 0.051300 | 9.31e-01 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 20 | 6.92e-01 | 0.051300 | 9.31e-01 |
| Transcriptional regulation of pluripotent stem cells | 28 | 6.40e-01 | -0.051100 | 9.14e-01 |
| Cell-Cell communication | 109 | 3.57e-01 | 0.051100 | 7.68e-01 |
| Eukaryotic Translation Termination | 48 | 5.42e-01 | 0.051000 | 8.70e-01 |
| Rab regulation of trafficking | 108 | 3.62e-01 | -0.050800 | 7.70e-01 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 31 | 6.26e-01 | 0.050600 | 9.04e-01 |
| Transport of Mature Transcript to Cytoplasm | 63 | 4.88e-01 | 0.050500 | 8.43e-01 |
| Vpr-mediated nuclear import of PICs | 24 | 6.69e-01 | 0.050500 | 9.26e-01 |
| Signaling by Rho GTPases | 342 | 1.11e-01 | -0.050300 | 6.34e-01 |
| ATF4 activates genes in response to endoplasmic reticulum stress | 23 | 6.78e-01 | 0.050100 | 9.31e-01 |
| Potassium Channels | 94 | 4.03e-01 | 0.049900 | 7.88e-01 |
| RHO GTPases activate PAKs | 21 | 6.92e-01 | -0.049900 | 9.31e-01 |
| MET promotes cell motility | 29 | 6.45e-01 | 0.049400 | 9.17e-01 |
| VEGFA-VEGFR2 Pathway | 92 | 4.18e-01 | -0.048900 | 7.95e-01 |
| Cargo recognition for clathrin-mediated endocytosis | 89 | 4.26e-01 | 0.048800 | 8.00e-01 |
| Ion channel transport | 156 | 2.95e-01 | 0.048600 | 7.32e-01 |
| Complex I biogenesis | 39 | 6.00e-01 | 0.048500 | 8.91e-01 |
| NIK-->noncanonical NF-kB signaling | 46 | 5.71e-01 | -0.048300 | 8.78e-01 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 50 | 5.55e-01 | -0.048200 | 8.70e-01 |
| Class I MHC mediated antigen processing & presentation | 310 | 1.46e-01 | 0.048100 | 6.70e-01 |
| Chaperone Mediated Autophagy | 18 | 7.24e-01 | -0.048000 | 9.36e-01 |
| Class B/2 (Secretin family receptors) | 82 | 4.56e-01 | 0.047600 | 8.20e-01 |
| Nonhomologous End-Joining (NHEJ) | 28 | 6.64e-01 | -0.047400 | 9.25e-01 |
| Acetylcholine binding and downstream events | 14 | 7.59e-01 | -0.047400 | 9.54e-01 |
| Postsynaptic nicotinic acetylcholine receptors | 14 | 7.59e-01 | -0.047400 | 9.54e-01 |
| Interleukin-10 signaling | 40 | 6.05e-01 | 0.047300 | 8.95e-01 |
| EPH-Ephrin signaling | 84 | 4.54e-01 | -0.047300 | 8.18e-01 |
| Signaling by VEGF | 98 | 4.20e-01 | -0.047200 | 7.95e-01 |
| Influenza Infection | 92 | 4.35e-01 | 0.047100 | 8.08e-01 |
| Regulation of PLK1 Activity at G2/M Transition | 73 | 4.87e-01 | 0.047000 | 8.43e-01 |
| Ub-specific processing proteases | 156 | 3.11e-01 | 0.047000 | 7.39e-01 |
| Abacavir transport and metabolism | 10 | 7.97e-01 | -0.046900 | 9.68e-01 |
| Nicotinate metabolism | 25 | 6.85e-01 | -0.046800 | 9.31e-01 |
| Recruitment of NuMA to mitotic centrosomes | 69 | 5.03e-01 | -0.046600 | 8.52e-01 |
| Translation | 186 | 2.74e-01 | -0.046500 | 7.27e-01 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | 23 | 6.99e-01 | -0.046500 | 9.31e-01 |
| RNA Polymerase III Transcription Initiation | 28 | 6.71e-01 | -0.046300 | 9.27e-01 |
| E2F mediated regulation of DNA replication | 19 | 7.27e-01 | 0.046200 | 9.36e-01 |
| Heme biosynthesis | 12 | 7.82e-01 | -0.046200 | 9.63e-01 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 18 | 7.35e-01 | -0.046100 | 9.41e-01 |
| SUMOylation of DNA replication proteins | 34 | 6.42e-01 | -0.046100 | 9.15e-01 |
| Scavenging by Class A Receptors | 17 | 7.42e-01 | 0.046000 | 9.47e-01 |
| mRNA decay by 3' to 5' exoribonuclease | 12 | 7.83e-01 | -0.046000 | 9.63e-01 |
| TRP channels | 24 | 6.97e-01 | 0.045900 | 9.31e-01 |
| C-type lectin receptors (CLRs) | 116 | 3.94e-01 | 0.045800 | 7.84e-01 |
| GPCR ligand binding | 403 | 1.17e-01 | 0.045600 | 6.34e-01 |
| Processing of Capped Intron-Containing Pre-mRNA | 182 | 2.89e-01 | 0.045600 | 7.27e-01 |
| Serotonin Neurotransmitter Release Cycle | 14 | 7.68e-01 | 0.045500 | 9.56e-01 |
| Transcription of the HIV genome | 54 | 5.63e-01 | -0.045500 | 8.72e-01 |
| Switching of origins to a post-replicative state | 75 | 4.98e-01 | -0.045300 | 8.49e-01 |
| DNA Damage Recognition in GG-NER | 28 | 6.79e-01 | -0.045300 | 9.31e-01 |
| Activation of the pre-replicative complex | 27 | 6.84e-01 | -0.045200 | 9.31e-01 |
| Diseases associated with glycosaminoglycan metabolism | 39 | 6.26e-01 | 0.045100 | 9.04e-01 |
| Synthesis of very long-chain fatty acyl-CoAs | 20 | 7.28e-01 | 0.044800 | 9.36e-01 |
| GP1b-IX-V activation signalling | 10 | 8.07e-01 | 0.044700 | 9.74e-01 |
| Antiviral mechanism by IFN-stimulated genes | 59 | 5.54e-01 | -0.044600 | 8.70e-01 |
| Activation of G protein gated Potassium channels | 24 | 7.07e-01 | -0.044300 | 9.31e-01 |
| G protein gated Potassium channels | 24 | 7.07e-01 | -0.044300 | 9.31e-01 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 24 | 7.07e-01 | -0.044300 | 9.31e-01 |
| Early Phase of HIV Life Cycle | 10 | 8.09e-01 | -0.044200 | 9.74e-01 |
| Triglyceride catabolism | 21 | 7.26e-01 | 0.044100 | 9.36e-01 |
| COPI-mediated anterograde transport | 74 | 5.12e-01 | -0.044100 | 8.57e-01 |
| Glucagon signaling in metabolic regulation | 28 | 6.87e-01 | 0.044100 | 9.31e-01 |
| RNA Polymerase III Transcription Termination | 18 | 7.47e-01 | -0.044000 | 9.49e-01 |
| Glutamate Neurotransmitter Release Cycle | 22 | 7.22e-01 | -0.043900 | 9.35e-01 |
| WNT ligand biogenesis and trafficking | 24 | 7.10e-01 | 0.043800 | 9.33e-01 |
| Transferrin endocytosis and recycling | 28 | 6.89e-01 | 0.043800 | 9.31e-01 |
| Digestion and absorption | 25 | 7.05e-01 | -0.043700 | 9.31e-01 |
| Signaling by Insulin receptor | 72 | 5.22e-01 | 0.043700 | 8.62e-01 |
| G2/M Checkpoints | 109 | 4.32e-01 | -0.043600 | 8.06e-01 |
| Formation of RNA Pol II elongation complex | 42 | 6.27e-01 | -0.043400 | 9.04e-01 |
| RNA Polymerase II Transcription Elongation | 42 | 6.27e-01 | -0.043400 | 9.04e-01 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 30 | 6.82e-01 | -0.043200 | 9.31e-01 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 77 | 5.13e-01 | 0.043100 | 8.57e-01 |
| Amplification of signal from the kinetochores | 77 | 5.13e-01 | 0.043100 | 8.57e-01 |
| FGFR4 ligand binding and activation | 13 | 7.88e-01 | -0.043000 | 9.65e-01 |
| Prolactin receptor signaling | 15 | 7.73e-01 | 0.043000 | 9.58e-01 |
| Vasopressin regulates renal water homeostasis via Aquaporins | 37 | 6.52e-01 | -0.042800 | 9.21e-01 |
| Hedgehog 'on' state | 71 | 5.34e-01 | -0.042700 | 8.70e-01 |
| GABA synthesis, release, reuptake and degradation | 17 | 7.61e-01 | 0.042600 | 9.54e-01 |
| Amine ligand-binding receptors | 39 | 6.46e-01 | 0.042600 | 9.17e-01 |
| Degradation of GLI2 by the proteasome | 47 | 6.15e-01 | -0.042400 | 8.99e-01 |
| Ethanol oxidation | 11 | 8.08e-01 | 0.042300 | 9.74e-01 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 11 | 8.11e-01 | -0.041700 | 9.74e-01 |
| VxPx cargo-targeting to cilium | 20 | 7.51e-01 | 0.041100 | 9.51e-01 |
| PI3K Cascade | 41 | 6.50e-01 | -0.040900 | 9.21e-01 |
| Potential therapeutics for SARS | 33 | 6.85e-01 | 0.040900 | 9.31e-01 |
| Methylation | 11 | 8.15e-01 | 0.040800 | 9.75e-01 |
| Tie2 Signaling | 17 | 7.71e-01 | 0.040800 | 9.57e-01 |
| Platelet activation, signaling and aggregation | 233 | 2.86e-01 | -0.040700 | 7.27e-01 |
| Interactions of Rev with host cellular proteins | 26 | 7.20e-01 | 0.040600 | 9.35e-01 |
| Regulation of expression of SLITs and ROBOs | 110 | 4.63e-01 | 0.040500 | 8.25e-01 |
| HATs acetylate histones | 65 | 5.72e-01 | -0.040500 | 8.78e-01 |
| Late endosomal microautophagy | 26 | 7.21e-01 | -0.040400 | 9.35e-01 |
| Retrograde neurotrophin signalling | 14 | 7.94e-01 | -0.040400 | 9.65e-01 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 111 | 4.67e-01 | 0.040000 | 8.28e-01 |
| Deubiquitination | 222 | 3.11e-01 | 0.039500 | 7.39e-01 |
| Organelle biogenesis and maintenance | 229 | 3.05e-01 | -0.039400 | 7.39e-01 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 15 | 7.93e-01 | 0.039200 | 9.65e-01 |
| NCAM signaling for neurite out-growth | 55 | 6.15e-01 | -0.039200 | 8.99e-01 |
| AURKA Activation by TPX2 | 62 | 5.94e-01 | -0.039200 | 8.89e-01 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 41 | 6.64e-01 | -0.039200 | 9.25e-01 |
| Triglyceride metabolism | 33 | 6.97e-01 | 0.039100 | 9.31e-01 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 60 | 6.00e-01 | 0.039100 | 8.91e-01 |
| DARPP-32 events | 21 | 7.57e-01 | 0.039100 | 9.54e-01 |
| Platelet degranulation | 114 | 4.72e-01 | -0.039000 | 8.32e-01 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 11 | 8.23e-01 | -0.039000 | 9.75e-01 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 62 | 5.96e-01 | -0.038900 | 8.90e-01 |
| Semaphorin interactions | 60 | 6.09e-01 | -0.038200 | 8.96e-01 |
| TP53 Regulates Transcription of Caspase Activators and Caspases | 10 | 8.35e-01 | 0.038100 | 9.80e-01 |
| Activation of BH3-only proteins | 28 | 7.28e-01 | 0.037900 | 9.36e-01 |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 10 | 8.36e-01 | -0.037800 | 9.80e-01 |
| Muscle contraction | 188 | 3.73e-01 | -0.037800 | 7.82e-01 |
| Apoptosis | 146 | 4.33e-01 | 0.037600 | 8.06e-01 |
| Nucleotide Excision Repair | 87 | 5.45e-01 | -0.037600 | 8.70e-01 |
| Regulation of actin dynamics for phagocytic cup formation | 66 | 5.99e-01 | -0.037500 | 8.91e-01 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 45 | 6.64e-01 | 0.037500 | 9.25e-01 |
| ADORA2B mediated anti-inflammatory cytokines production | 121 | 4.77e-01 | 0.037500 | 8.37e-01 |
| APC-Cdc20 mediated degradation of Nek2A | 21 | 7.66e-01 | -0.037500 | 9.56e-01 |
| HCMV Early Events | 47 | 6.57e-01 | 0.037400 | 9.24e-01 |
| Presynaptic phase of homologous DNA pairing and strand exchange | 33 | 7.11e-01 | -0.037300 | 9.33e-01 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 33 | 7.15e-01 | -0.036700 | 9.35e-01 |
| Diseases of mitotic cell cycle | 33 | 7.15e-01 | -0.036700 | 9.35e-01 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 73 | 5.88e-01 | 0.036700 | 8.84e-01 |
| Degradation of beta-catenin by the destruction complex | 71 | 5.93e-01 | -0.036700 | 8.89e-01 |
| Orc1 removal from chromatin | 57 | 6.37e-01 | -0.036100 | 9.14e-01 |
| Disease | 1235 | 3.49e-02 | -0.036100 | 4.69e-01 |
| B-WICH complex positively regulates rRNA expression | 24 | 7.61e-01 | -0.035900 | 9.54e-01 |
| Post-translational modification: synthesis of GPI-anchored proteins | 75 | 5.92e-01 | -0.035800 | 8.88e-01 |
| HIV Infection | 179 | 4.10e-01 | -0.035800 | 7.92e-01 |
| Detoxification of Reactive Oxygen Species | 29 | 7.40e-01 | 0.035600 | 9.45e-01 |
| Activation of GABAB receptors | 38 | 7.06e-01 | 0.035400 | 9.31e-01 |
| GABA B receptor activation | 38 | 7.06e-01 | 0.035400 | 9.31e-01 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 99 | 5.44e-01 | 0.035300 | 8.70e-01 |
| Acetylcholine Neurotransmitter Release Cycle | 14 | 8.19e-01 | 0.035300 | 9.75e-01 |
| Degradation of GLI1 by the proteasome | 48 | 6.74e-01 | -0.035100 | 9.28e-01 |
| FGFR2 mutant receptor activation | 26 | 7.57e-01 | 0.035100 | 9.54e-01 |
| Synthesis of PC | 25 | 7.62e-01 | -0.035000 | 9.54e-01 |
| Mitotic Anaphase | 194 | 4.01e-01 | -0.035000 | 7.88e-01 |
| Regulation of Complement cascade | 45 | 6.86e-01 | -0.034800 | 9.31e-01 |
| Programmed Cell Death | 149 | 4.64e-01 | 0.034800 | 8.25e-01 |
| IRS-related events triggered by IGF1R | 49 | 6.77e-01 | 0.034400 | 9.31e-01 |
| SARS-CoV-1 Infection | 38 | 7.14e-01 | -0.034400 | 9.35e-01 |
| Insulin receptor signalling cascade | 51 | 6.71e-01 | 0.034400 | 9.27e-01 |
| Signaling by the B Cell Receptor (BCR) | 100 | 5.54e-01 | 0.034300 | 8.70e-01 |
| Viral mRNA Translation | 45 | 6.91e-01 | 0.034300 | 9.31e-01 |
| Diseases associated with the TLR signaling cascade | 20 | 7.91e-01 | -0.034300 | 9.65e-01 |
| Diseases of Immune System | 20 | 7.91e-01 | -0.034300 | 9.65e-01 |
| Signaling by RAF1 mutants | 38 | 7.17e-01 | 0.033900 | 9.35e-01 |
| G beta:gamma signalling through BTK | 13 | 8.33e-01 | -0.033800 | 9.79e-01 |
| PKA activation in glucagon signalling | 16 | 8.16e-01 | 0.033700 | 9.75e-01 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | 19 | 8.02e-01 | 0.033200 | 9.71e-01 |
| Mitotic Metaphase and Anaphase | 195 | 4.27e-01 | -0.033100 | 8.00e-01 |
| Formation of TC-NER Pre-Incision Complex | 39 | 7.21e-01 | 0.033000 | 9.35e-01 |
| Condensation of Prophase Chromosomes | 10 | 8.57e-01 | -0.032900 | 9.81e-01 |
| IGF1R signaling cascade | 50 | 6.90e-01 | 0.032700 | 9.31e-01 |
| Cell-extracellular matrix interactions | 14 | 8.33e-01 | -0.032600 | 9.79e-01 |
| Regulation of insulin secretion | 70 | 6.39e-01 | -0.032400 | 9.14e-01 |
| Toll-like Receptor Cascades | 131 | 5.31e-01 | 0.031700 | 8.70e-01 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 50 | 6.99e-01 | 0.031600 | 9.31e-01 |
| Cargo trafficking to the periciliary membrane | 43 | 7.20e-01 | 0.031600 | 9.35e-01 |
| mRNA Splicing - Major Pathway | 134 | 5.30e-01 | 0.031500 | 8.70e-01 |
| Rev-mediated nuclear export of HIV RNA | 25 | 7.86e-01 | 0.031500 | 9.65e-01 |
| FCERI mediated NF-kB activation | 69 | 6.52e-01 | 0.031400 | 9.21e-01 |
| Signaling by SCF-KIT | 43 | 7.24e-01 | -0.031100 | 9.36e-01 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 58 | 6.83e-01 | 0.031000 | 9.31e-01 |
| Amino acids regulate mTORC1 | 47 | 7.18e-01 | 0.030500 | 9.35e-01 |
| Lysine catabolism | 12 | 8.56e-01 | -0.030300 | 9.81e-01 |
| Triglyceride biosynthesis | 12 | 8.56e-01 | 0.030300 | 9.81e-01 |
| VEGFR2 mediated vascular permeability | 27 | 7.86e-01 | 0.030200 | 9.65e-01 |
| Golgi Associated Vesicle Biogenesis | 48 | 7.17e-01 | 0.030200 | 9.35e-01 |
| Downstream signaling events of B Cell Receptor (BCR) | 68 | 6.69e-01 | 0.030000 | 9.26e-01 |
| Cyclin A:Cdk2-associated events at S phase entry | 72 | 6.61e-01 | -0.029900 | 9.24e-01 |
| Phase 4 - resting membrane potential | 18 | 8.27e-01 | -0.029800 | 9.77e-01 |
| Signalling to RAS | 20 | 8.19e-01 | -0.029600 | 9.75e-01 |
| trans-Golgi Network Vesicle Budding | 61 | 6.92e-01 | -0.029400 | 9.31e-01 |
| SUMOylation of DNA damage response and repair proteins | 56 | 7.04e-01 | -0.029300 | 9.31e-01 |
| Eicosanoid ligand-binding receptors | 13 | 8.55e-01 | 0.029300 | 9.81e-01 |
| Signaling by FGFR in disease | 55 | 7.09e-01 | 0.029100 | 9.33e-01 |
| Protein folding | 86 | 6.41e-01 | -0.029100 | 9.15e-01 |
| Signaling by NOTCH3 | 41 | 7.51e-01 | -0.028700 | 9.51e-01 |
| G-protein activation | 23 | 8.13e-01 | 0.028500 | 9.75e-01 |
| G alpha (i) signalling events | 351 | 3.61e-01 | 0.028500 | 7.70e-01 |
| Signaling by Nuclear Receptors | 216 | 4.71e-01 | -0.028500 | 8.32e-01 |
| COPII-mediated vesicle transport | 57 | 7.11e-01 | -0.028400 | 9.33e-01 |
| mRNA Splicing | 142 | 5.60e-01 | 0.028400 | 8.70e-01 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 51 | 7.27e-01 | 0.028300 | 9.36e-01 |
| The citric acid (TCA) cycle and respiratory electron transport | 118 | 5.97e-01 | 0.028200 | 8.91e-01 |
| RNA Polymerase II Transcription | 970 | 1.43e-01 | 0.028000 | 6.70e-01 |
| ERK/MAPK targets | 22 | 8.21e-01 | 0.027900 | 9.75e-01 |
| Lewis blood group biosynthesis | 12 | 8.68e-01 | -0.027700 | 9.81e-01 |
| Budding and maturation of HIV virion | 20 | 8.31e-01 | -0.027500 | 9.79e-01 |
| ER to Golgi Anterograde Transport | 117 | 6.09e-01 | -0.027400 | 8.96e-01 |
| Sema3A PAK dependent Axon repulsion | 15 | 8.54e-01 | -0.027400 | 9.81e-01 |
| eNOS activation | 10 | 8.81e-01 | -0.027300 | 9.81e-01 |
| Aspartate and asparagine metabolism | 11 | 8.76e-01 | -0.027200 | 9.81e-01 |
| G-protein beta:gamma signalling | 26 | 8.11e-01 | -0.027100 | 9.74e-01 |
| Signaling by cytosolic FGFR1 fusion mutants | 18 | 8.45e-01 | 0.026600 | 9.81e-01 |
| Peptide ligand-binding receptors | 172 | 5.47e-01 | 0.026600 | 8.70e-01 |
| G1/S Transition | 110 | 6.30e-01 | -0.026600 | 9.05e-01 |
| Generation of second messenger molecules | 26 | 8.15e-01 | -0.026500 | 9.75e-01 |
| RORA activates gene expression | 17 | 8.51e-01 | -0.026300 | 9.81e-01 |
| Ion transport by P-type ATPases | 48 | 7.53e-01 | -0.026300 | 9.53e-01 |
| SUMOylation | 142 | 5.91e-01 | -0.026200 | 8.87e-01 |
| FGFR1 ligand binding and activation | 15 | 8.63e-01 | -0.025800 | 9.81e-01 |
| Regulation of localization of FOXO transcription factors | 12 | 8.78e-01 | 0.025700 | 9.81e-01 |
| Transport of the SLBP Dependant Mature mRNA | 25 | 8.25e-01 | 0.025600 | 9.76e-01 |
| Peptide chain elongation | 45 | 7.71e-01 | 0.025100 | 9.57e-01 |
| Hemostasis | 537 | 3.23e-01 | -0.025000 | 7.47e-01 |
| NF-kB is activated and signals survival | 10 | 8.92e-01 | 0.024900 | 9.81e-01 |
| S Phase | 139 | 6.15e-01 | -0.024700 | 8.99e-01 |
| Mitotic Spindle Checkpoint | 92 | 6.85e-01 | 0.024500 | 9.31e-01 |
| M Phase | 295 | 4.73e-01 | -0.024300 | 8.34e-01 |
| Intrinsic Pathway for Apoptosis | 44 | 7.80e-01 | -0.024300 | 9.62e-01 |
| Mitotic G1 phase and G1/S transition | 126 | 6.38e-01 | -0.024300 | 9.14e-01 |
| G alpha (q) signalling events | 195 | 5.60e-01 | 0.024200 | 8.70e-01 |
| Cellular Senescence | 115 | 6.55e-01 | -0.024200 | 9.22e-01 |
| Loss of Nlp from mitotic centrosomes | 60 | 7.47e-01 | -0.024100 | 9.49e-01 |
| Loss of proteins required for interphase microtubule organization from the centrosome | 60 | 7.47e-01 | -0.024100 | 9.49e-01 |
| Interleukin-1 family signaling | 117 | 6.59e-01 | 0.023700 | 9.24e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE | 20 | 8.55e-01 | -0.023600 | 9.81e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 20 | 8.55e-01 | -0.023600 | 9.81e-01 |
| Interleukin-12 family signaling | 48 | 7.78e-01 | 0.023500 | 9.60e-01 |
| Signaling by PDGF | 52 | 7.71e-01 | -0.023400 | 9.57e-01 |
| Collagen biosynthesis and modifying enzymes | 61 | 7.54e-01 | -0.023300 | 9.53e-01 |
| G2/M Transition | 153 | 6.20e-01 | -0.023200 | 9.01e-01 |
| GLI3 is processed to GLI3R by the proteasome | 47 | 7.83e-01 | -0.023200 | 9.63e-01 |
| RHO GTPases activate PKNs | 31 | 8.24e-01 | 0.023100 | 9.75e-01 |
| Vesicle-mediated transport | 573 | 3.46e-01 | -0.023100 | 7.63e-01 |
| Synthesis of glycosylphosphatidylinositol (GPI) | 14 | 8.81e-01 | -0.023100 | 9.81e-01 |
| Transcriptional regulation of white adipocyte differentiation | 75 | 7.29e-01 | 0.023100 | 9.36e-01 |
| SUMOylation of intracellular receptors | 28 | 8.33e-01 | -0.023100 | 9.79e-01 |
| Signaling by Receptor Tyrosine Kinases | 457 | 4.04e-01 | 0.022900 | 7.88e-01 |
| Adaptive Immune System | 609 | 3.42e-01 | 0.022700 | 7.61e-01 |
| RNA Polymerase III Abortive And Retractive Initiation | 33 | 8.22e-01 | -0.022600 | 9.75e-01 |
| RNA Polymerase III Transcription | 33 | 8.22e-01 | -0.022600 | 9.75e-01 |
| Transcriptional regulation by small RNAs | 33 | 8.23e-01 | -0.022500 | 9.75e-01 |
| Initiation of Nuclear Envelope (NE) Reformation | 18 | 8.70e-01 | -0.022300 | 9.81e-01 |
| Activation of NF-kappaB in B cells | 56 | 7.73e-01 | -0.022300 | 9.58e-01 |
| Cell Cycle | 525 | 3.84e-01 | -0.022300 | 7.82e-01 |
| Innate Immune System | 863 | 2.76e-01 | -0.022000 | 7.27e-01 |
| Late Phase of HIV Life Cycle | 101 | 7.03e-01 | -0.022000 | 9.31e-01 |
| RHO GTPase Effectors | 220 | 5.80e-01 | -0.021700 | 8.83e-01 |
| Metabolism of cofactors | 19 | 8.70e-01 | -0.021700 | 9.81e-01 |
| Collagen chain trimerization | 42 | 8.11e-01 | -0.021400 | 9.74e-01 |
| Postmitotic nuclear pore complex (NPC) reformation | 20 | 8.69e-01 | -0.021300 | 9.81e-01 |
| Ephrin signaling | 19 | 8.73e-01 | 0.021200 | 9.81e-01 |
| Dectin-2 family | 21 | 8.68e-01 | 0.021000 | 9.81e-01 |
| Recycling pathway of L1 | 27 | 8.51e-01 | 0.020900 | 9.81e-01 |
| Inflammasomes | 18 | 8.79e-01 | -0.020700 | 9.81e-01 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 13 | 8.97e-01 | 0.020700 | 9.81e-01 |
| Mitotic G2-G2/M phases | 155 | 6.58e-01 | -0.020600 | 9.24e-01 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 23 | 8.65e-01 | -0.020500 | 9.81e-01 |
| Signaling by NTRKs | 131 | 6.87e-01 | 0.020400 | 9.31e-01 |
| Anchoring of the basal body to the plasma membrane | 82 | 7.51e-01 | -0.020300 | 9.51e-01 |
| Metabolism of proteins | 1584 | 1.85e-01 | -0.020200 | 6.82e-01 |
| Interaction between L1 and Ankyrins | 28 | 8.54e-01 | -0.020100 | 9.81e-01 |
| Synthesis of PIPs at the plasma membrane | 52 | 8.02e-01 | 0.020100 | 9.71e-01 |
| Sphingolipid de novo biosynthesis | 38 | 8.30e-01 | 0.020100 | 9.79e-01 |
| Transport of the SLBP independent Mature mRNA | 24 | 8.66e-01 | 0.019900 | 9.81e-01 |
| Eukaryotic Translation Elongation | 48 | 8.15e-01 | 0.019500 | 9.75e-01 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 16 | 8.93e-01 | 0.019400 | 9.81e-01 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 16 | 8.93e-01 | 0.019400 | 9.81e-01 |
| Purine catabolism | 17 | 8.91e-01 | 0.019200 | 9.81e-01 |
| Cilium Assembly | 162 | 6.74e-01 | -0.019200 | 9.28e-01 |
| Calnexin/calreticulin cycle | 17 | 8.91e-01 | -0.019200 | 9.81e-01 |
| Biosynthesis of DHA-derived SPMs | 16 | 8.95e-01 | 0.019100 | 9.81e-01 |
| Leishmania infection | 236 | 6.15e-01 | -0.019100 | 8.99e-01 |
| Cell Cycle, Mitotic | 419 | 5.05e-01 | -0.019000 | 8.54e-01 |
| Endogenous sterols | 25 | 8.71e-01 | 0.018700 | 9.81e-01 |
| MTOR signalling | 35 | 8.48e-01 | -0.018700 | 9.81e-01 |
| Axon guidance | 445 | 5.03e-01 | 0.018600 | 8.52e-01 |
| HIV Life Cycle | 110 | 7.37e-01 | -0.018500 | 9.42e-01 |
| Amyloid fiber formation | 43 | 8.34e-01 | 0.018400 | 9.80e-01 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | 50 | 8.22e-01 | -0.018400 | 9.75e-01 |
| Processing of DNA double-strand break ends | 52 | 8.19e-01 | -0.018400 | 9.75e-01 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 14 | 9.05e-01 | -0.018400 | 9.84e-01 |
| Membrane Trafficking | 535 | 4.77e-01 | -0.018100 | 8.37e-01 |
| Nervous system development | 468 | 5.06e-01 | 0.018000 | 8.54e-01 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 35 | 8.54e-01 | 0.018000 | 9.81e-01 |
| Formation of Fibrin Clot (Clotting Cascade) | 36 | 8.54e-01 | 0.017800 | 9.81e-01 |
| RNA Polymerase II Pre-transcription Events | 63 | 8.09e-01 | -0.017600 | 9.74e-01 |
| Mitotic Prophase | 66 | 8.05e-01 | 0.017600 | 9.73e-01 |
| Oxidative Stress Induced Senescence | 58 | 8.18e-01 | -0.017500 | 9.75e-01 |
| Cell junction organization | 76 | 7.93e-01 | -0.017400 | 9.65e-01 |
| Influenza Viral RNA Transcription and Replication | 77 | 7.94e-01 | 0.017200 | 9.65e-01 |
| RHO GTPases Activate WASPs and WAVEs | 35 | 8.60e-01 | 0.017200 | 9.81e-01 |
| TAK1 activates NFkB by phosphorylation and activation of IKKs complex | 22 | 8.89e-01 | 0.017200 | 9.81e-01 |
| Metabolism of porphyrins | 25 | 8.84e-01 | -0.016800 | 9.81e-01 |
| Downstream signal transduction | 29 | 8.76e-01 | 0.016800 | 9.81e-01 |
| Transport to the Golgi and subsequent modification | 144 | 7.29e-01 | -0.016800 | 9.36e-01 |
| CTLA4 inhibitory signaling | 21 | 8.95e-01 | -0.016600 | 9.81e-01 |
| Mitotic Prometaphase | 158 | 7.19e-01 | 0.016600 | 9.35e-01 |
| Signaling by NTRK1 (TRKA) | 113 | 7.61e-01 | 0.016600 | 9.54e-01 |
| Toll Like Receptor 4 (TLR4) Cascade | 110 | 7.68e-01 | 0.016300 | 9.56e-01 |
| Costimulation by the CD28 family | 60 | 8.29e-01 | -0.016100 | 9.79e-01 |
| RAF-independent MAPK1/3 activation | 23 | 8.94e-01 | -0.016000 | 9.81e-01 |
| Immune System | 1753 | 2.75e-01 | -0.015900 | 7.27e-01 |
| FGFR1 mutant receptor activation | 30 | 8.81e-01 | 0.015800 | 9.81e-01 |
| Transport of Mature mRNA Derived from an Intronless Transcript | 30 | 8.81e-01 | -0.015800 | 9.81e-01 |
| NoRC negatively regulates rRNA expression | 34 | 8.74e-01 | -0.015700 | 9.81e-01 |
| Signaling by Erythropoietin | 24 | 8.95e-01 | 0.015500 | 9.81e-01 |
| Presynaptic function of Kainate receptors | 16 | 9.15e-01 | -0.015500 | 9.85e-01 |
| Classical antibody-mediated complement activation | 13 | 9.24e-01 | 0.015300 | 9.89e-01 |
| Clathrin-mediated endocytosis | 126 | 7.67e-01 | 0.015300 | 9.56e-01 |
| Intraflagellar transport | 38 | 8.73e-01 | -0.015000 | 9.81e-01 |
| Gene expression (Transcription) | 1079 | 4.14e-01 | 0.014900 | 7.94e-01 |
| Nicotinamide salvaging | 15 | 9.21e-01 | -0.014800 | 9.89e-01 |
| Deactivation of the beta-catenin transactivating complex | 34 | 8.82e-01 | -0.014700 | 9.81e-01 |
| RHO GTPases Activate ROCKs | 18 | 9.14e-01 | -0.014700 | 9.85e-01 |
| Post-translational protein modification | 1148 | 4.11e-01 | -0.014500 | 7.92e-01 |
| SUMO E3 ligases SUMOylate target proteins | 136 | 7.71e-01 | -0.014500 | 9.57e-01 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 30 | 8.92e-01 | -0.014400 | 9.81e-01 |
| Activation of Matrix Metalloproteinases | 29 | 8.94e-01 | -0.014400 | 9.81e-01 |
| PI3K/AKT Signaling in Cancer | 98 | 8.06e-01 | 0.014300 | 9.74e-01 |
| TNFR1-induced NFkappaB signaling pathway | 24 | 9.05e-01 | -0.014100 | 9.84e-01 |
| ECM proteoglycans | 54 | 8.58e-01 | -0.014100 | 9.81e-01 |
| tRNA processing in the nucleus | 47 | 8.67e-01 | 0.014100 | 9.81e-01 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | 162 | 7.57e-01 | 0.014100 | 9.54e-01 |
| NGF-stimulated transcription | 39 | 8.79e-01 | -0.014100 | 9.81e-01 |
| mRNA Capping | 21 | 9.11e-01 | -0.014100 | 9.84e-01 |
| Generic Transcription Pathway | 872 | 4.87e-01 | 0.014000 | 8.43e-01 |
| CRMPs in Sema3A signaling | 15 | 9.26e-01 | -0.013800 | 9.89e-01 |
| L1CAM interactions | 95 | 8.16e-01 | 0.013800 | 9.75e-01 |
| Cellular response to hypoxia | 59 | 8.54e-01 | -0.013800 | 9.81e-01 |
| CD28 dependent PI3K/Akt signaling | 21 | 9.14e-01 | 0.013700 | 9.85e-01 |
| Cell Cycle Checkpoints | 213 | 7.34e-01 | -0.013500 | 9.41e-01 |
| Activation of kainate receptors upon glutamate binding | 25 | 9.08e-01 | 0.013300 | 9.84e-01 |
| Polo-like kinase mediated events | 13 | 9.34e-01 | -0.013300 | 9.90e-01 |
| Nucleobase catabolism | 33 | 8.95e-01 | 0.013200 | 9.81e-01 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 41 | 8.84e-01 | -0.013200 | 9.81e-01 |
| Signaling by RAS mutants | 41 | 8.84e-01 | -0.013200 | 9.81e-01 |
| Signaling by moderate kinase activity BRAF mutants | 41 | 8.84e-01 | -0.013200 | 9.81e-01 |
| Signaling downstream of RAS mutants | 41 | 8.84e-01 | -0.013200 | 9.81e-01 |
| MAPK family signaling cascades | 287 | 7.02e-01 | -0.013200 | 9.31e-01 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 12 | 9.37e-01 | -0.013100 | 9.91e-01 |
| Mitochondrial Fatty Acid Beta-Oxidation | 30 | 9.02e-01 | -0.012900 | 9.82e-01 |
| Formation of a pool of free 40S subunits | 54 | 8.70e-01 | 0.012900 | 9.81e-01 |
| Nitric oxide stimulates guanylate cyclase | 22 | 9.17e-01 | 0.012900 | 9.85e-01 |
| ISG15 antiviral mechanism | 53 | 8.72e-01 | 0.012800 | 9.81e-01 |
| Common Pathway of Fibrin Clot Formation | 20 | 9.21e-01 | 0.012800 | 9.89e-01 |
| Trafficking and processing of endosomal TLR | 11 | 9.42e-01 | -0.012600 | 9.91e-01 |
| Separation of Sister Chromatids | 141 | 7.97e-01 | -0.012600 | 9.68e-01 |
| MAP2K and MAPK activation | 35 | 8.97e-01 | 0.012600 | 9.81e-01 |
| Metabolic disorders of biological oxidation enzymes | 33 | 9.01e-01 | -0.012500 | 9.82e-01 |
| Nuclear import of Rev protein | 24 | 9.16e-01 | 0.012500 | 9.85e-01 |
| p75NTR signals via NF-kB | 11 | 9.43e-01 | -0.012400 | 9.91e-01 |
| HCMV Infection | 65 | 8.64e-01 | -0.012300 | 9.81e-01 |
| Rap1 signalling | 15 | 9.34e-01 | -0.012300 | 9.90e-01 |
| DNA Damage/Telomere Stress Induced Senescence | 25 | 9.16e-01 | -0.012200 | 9.85e-01 |
| Anti-inflammatory response favouring Leishmania parasite infection | 160 | 7.94e-01 | 0.012000 | 9.65e-01 |
| Leishmania parasite growth and survival | 160 | 7.94e-01 | 0.012000 | 9.65e-01 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 48 | 8.86e-01 | -0.012000 | 9.81e-01 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 48 | 8.86e-01 | -0.012000 | 9.81e-01 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 48 | 8.86e-01 | -0.012000 | 9.81e-01 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 48 | 8.86e-01 | -0.012000 | 9.81e-01 |
| Signaling by NOTCH1 in Cancer | 48 | 8.86e-01 | -0.012000 | 9.81e-01 |
| NRIF signals cell death from the nucleus | 11 | 9.46e-01 | -0.011900 | 9.91e-01 |
| Infectious disease | 601 | 6.23e-01 | -0.011800 | 9.04e-01 |
| RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | 10 | 9.49e-01 | -0.011700 | 9.92e-01 |
| Signaling by MET | 63 | 8.73e-01 | 0.011600 | 9.81e-01 |
| Cellular responses to stress | 393 | 6.95e-01 | 0.011600 | 9.31e-01 |
| Adrenaline,noradrenaline inhibits insulin secretion | 23 | 9.25e-01 | 0.011400 | 9.89e-01 |
| Glycosaminoglycan metabolism | 109 | 8.38e-01 | 0.011300 | 9.81e-01 |
| Biosynthesis of specialized proresolving mediators (SPMs) | 18 | 9.34e-01 | -0.011300 | 9.90e-01 |
| Signaling by PDGFR in disease | 19 | 9.33e-01 | 0.011100 | 9.90e-01 |
| SARS-CoV Infections | 70 | 8.73e-01 | -0.011000 | 9.81e-01 |
| G2/M DNA damage checkpoint | 51 | 8.92e-01 | -0.011000 | 9.81e-01 |
| Signal transduction by L1 | 19 | 9.35e-01 | 0.010900 | 9.90e-01 |
| Signaling by WNT | 237 | 7.75e-01 | -0.010800 | 9.58e-01 |
| Cap-dependent Translation Initiation | 66 | 8.80e-01 | -0.010700 | 9.81e-01 |
| Eukaryotic Translation Initiation | 66 | 8.80e-01 | -0.010700 | 9.81e-01 |
| SUMOylation of RNA binding proteins | 36 | 9.11e-01 | -0.010700 | 9.84e-01 |
| MAPK1/MAPK3 signaling | 251 | 7.76e-01 | -0.010500 | 9.58e-01 |
| Translation of structural proteins | 22 | 9.33e-01 | -0.010400 | 9.90e-01 |
| Nuclear Envelope Breakdown | 41 | 9.09e-01 | 0.010300 | 9.84e-01 |
| Hedgehog 'off' state | 86 | 8.71e-01 | -0.010100 | 9.81e-01 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | 31 | 9.23e-01 | -0.010000 | 9.89e-01 |
| Downstream TCR signaling | 76 | 8.80e-01 | -0.010000 | 9.81e-01 |
| Regulation of RAS by GAPs | 56 | 8.99e-01 | -0.009840 | 9.82e-01 |
| Selenoamino acid metabolism | 62 | 8.94e-01 | -0.009810 | 9.81e-01 |
| Antimicrobial peptides | 55 | 9.00e-01 | -0.009780 | 9.82e-01 |
| Nuclear Receptor transcription pathway | 52 | 9.08e-01 | -0.009270 | 9.84e-01 |
| Ca2+ pathway | 55 | 9.07e-01 | -0.009120 | 9.84e-01 |
| PI Metabolism | 79 | 8.89e-01 | -0.009110 | 9.81e-01 |
| Cellular response to heat stress | 74 | 8.94e-01 | 0.008950 | 9.81e-01 |
| Attenuation phase | 19 | 9.47e-01 | 0.008850 | 9.92e-01 |
| Creation of C4 and C2 activators | 20 | 9.46e-01 | 0.008830 | 9.91e-01 |
| Negative regulation of MAPK pathway | 39 | 9.24e-01 | -0.008780 | 9.89e-01 |
| Smooth Muscle Contraction | 35 | 9.30e-01 | -0.008570 | 9.90e-01 |
| Interleukin-1 signaling | 82 | 8.95e-01 | 0.008450 | 9.81e-01 |
| Diseases of signal transduction by growth factor receptors and second messengers | 337 | 7.91e-01 | -0.008430 | 9.65e-01 |
| TCR signaling | 97 | 8.92e-01 | 0.008000 | 9.81e-01 |
| N-Glycan antennae elongation | 14 | 9.59e-01 | -0.007980 | 9.93e-01 |
| SUMOylation of ubiquitinylation proteins | 28 | 9.43e-01 | -0.007880 | 9.91e-01 |
| Transcriptional Regulation by E2F6 | 30 | 9.41e-01 | -0.007840 | 9.91e-01 |
| Neurexins and neuroligins | 54 | 9.22e-01 | 0.007680 | 9.89e-01 |
| Interconversion of nucleotide di- and triphosphates | 25 | 9.48e-01 | -0.007610 | 9.92e-01 |
| Signaling by Interleukins | 394 | 8.02e-01 | -0.007370 | 9.71e-01 |
| Activation of ATR in response to replication stress | 29 | 9.46e-01 | -0.007310 | 9.91e-01 |
| TNF signaling | 34 | 9.43e-01 | 0.007130 | 9.91e-01 |
| Signaling by Hedgehog | 118 | 8.95e-01 | -0.007040 | 9.81e-01 |
| RAF/MAP kinase cascade | 245 | 8.55e-01 | -0.006780 | 9.81e-01 |
| Phospholipase C-mediated cascade; FGFR4 | 14 | 9.66e-01 | -0.006660 | 9.93e-01 |
| Viral Messenger RNA Synthesis | 29 | 9.52e-01 | -0.006390 | 9.93e-01 |
| FGFR1c ligand binding and activation | 11 | 9.71e-01 | -0.006340 | 9.93e-01 |
| Signaling by activated point mutants of FGFR1 | 11 | 9.71e-01 | -0.006340 | 9.93e-01 |
| TCF dependent signaling in response to WNT | 152 | 8.93e-01 | -0.006330 | 9.81e-01 |
| Selenocysteine synthesis | 48 | 9.41e-01 | 0.006230 | 9.91e-01 |
| MAPK3 (ERK1) activation | 10 | 9.73e-01 | -0.006190 | 9.93e-01 |
| Signaling by NOTCH1 | 63 | 9.35e-01 | 0.005980 | 9.90e-01 |
| cGMP effects | 16 | 9.67e-01 | -0.005950 | 9.93e-01 |
| Beta defensins | 22 | 9.62e-01 | -0.005890 | 9.93e-01 |
| Signal amplification | 27 | 9.58e-01 | 0.005840 | 9.93e-01 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 23 | 9.62e-01 | 0.005780 | 9.93e-01 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 23 | 9.62e-01 | 0.005780 | 9.93e-01 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 78 | 9.31e-01 | -0.005700 | 9.90e-01 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 13 | 9.73e-01 | -0.005500 | 9.93e-01 |
| Defective EXT2 causes exostoses 2 | 13 | 9.73e-01 | -0.005500 | 9.93e-01 |
| Developmental Biology | 820 | 7.92e-01 | 0.005460 | 9.65e-01 |
| TP53 Regulates Metabolic Genes | 74 | 9.37e-01 | -0.005330 | 9.91e-01 |
| SUMOylation of chromatin organization proteins | 44 | 9.52e-01 | 0.005260 | 9.93e-01 |
| Estrogen-dependent gene expression | 83 | 9.35e-01 | 0.005200 | 9.90e-01 |
| SUMOylation of SUMOylation proteins | 23 | 9.66e-01 | -0.005190 | 9.93e-01 |
| PIP3 activates AKT signaling | 241 | 8.90e-01 | -0.005160 | 9.81e-01 |
| Neddylation | 193 | 9.02e-01 | 0.005120 | 9.82e-01 |
| Defensins | 24 | 9.66e-01 | 0.005080 | 9.93e-01 |
| Cyclin E associated events during G1/S transition | 70 | 9.42e-01 | -0.005010 | 9.91e-01 |
| Phospholipase C-mediated cascade: FGFR1 | 16 | 9.73e-01 | 0.004940 | 9.93e-01 |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | 11 | 9.78e-01 | 0.004870 | 9.93e-01 |
| Oncogenic MAPK signaling | 73 | 9.44e-01 | 0.004790 | 9.91e-01 |
| FOXO-mediated transcription of cell death genes | 14 | 9.76e-01 | -0.004580 | 9.93e-01 |
| Regulation of RUNX1 Expression and Activity | 16 | 9.75e-01 | 0.004490 | 9.93e-01 |
| FLT3 Signaling | 259 | 9.02e-01 | -0.004440 | 9.82e-01 |
| HIV Transcription Initiation | 38 | 9.62e-01 | -0.004430 | 9.93e-01 |
| RNA Polymerase II HIV Promoter Escape | 38 | 9.62e-01 | -0.004430 | 9.93e-01 |
| RNA Polymerase II Promoter Escape | 38 | 9.62e-01 | -0.004430 | 9.93e-01 |
| RNA Polymerase II Transcription Initiation | 38 | 9.62e-01 | -0.004430 | 9.93e-01 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 38 | 9.62e-01 | -0.004430 | 9.93e-01 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 38 | 9.62e-01 | -0.004430 | 9.93e-01 |
| Cardiac conduction | 126 | 9.35e-01 | -0.004230 | 9.90e-01 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 26 | 9.71e-01 | -0.004180 | 9.93e-01 |
| Interleukin-35 Signalling | 12 | 9.81e-01 | 0.004020 | 9.93e-01 |
| CLEC7A (Dectin-1) signaling | 83 | 9.52e-01 | 0.003830 | 9.93e-01 |
| Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon | 14 | 9.81e-01 | 0.003630 | 9.93e-01 |
| Pyruvate metabolism and Citric Acid (TCA) cycle | 44 | 9.67e-01 | 0.003580 | 9.93e-01 |
| Defects in vitamin and cofactor metabolism | 15 | 9.82e-01 | -0.003450 | 9.93e-01 |
| Chaperonin-mediated protein folding | 80 | 9.58e-01 | -0.003400 | 9.93e-01 |
| Cytokine Signaling in Immune system | 742 | 8.77e-01 | 0.003360 | 9.81e-01 |
| Platelet calcium homeostasis | 26 | 9.77e-01 | -0.003300 | 9.93e-01 |
| RAF activation | 31 | 9.75e-01 | 0.003280 | 9.93e-01 |
| Cellular responses to external stimuli | 400 | 9.11e-01 | 0.003260 | 9.84e-01 |
| Intracellular signaling by second messengers | 277 | 9.30e-01 | 0.003060 | 9.90e-01 |
| NOTCH3 Intracellular Domain Regulates Transcription | 23 | 9.80e-01 | 0.003020 | 9.93e-01 |
| VEGFR2 mediated cell proliferation | 19 | 9.82e-01 | 0.002980 | 9.93e-01 |
| Metabolism of RNA | 508 | 9.10e-01 | -0.002940 | 9.84e-01 |
| Negative epigenetic regulation of rRNA expression | 37 | 9.76e-01 | -0.002890 | 9.93e-01 |
| GPVI-mediated activation cascade | 29 | 9.81e-01 | 0.002580 | 9.93e-01 |
| SRP-dependent cotranslational protein targeting to membrane | 63 | 9.76e-01 | -0.002170 | 9.93e-01 |
| Bile acid and bile salt metabolism | 36 | 9.83e-01 | -0.002000 | 9.93e-01 |
| Interferon alpha/beta signaling | 55 | 9.80e-01 | 0.001960 | 9.93e-01 |
| Signaling by BRAF and RAF fusions | 58 | 9.80e-01 | 0.001940 | 9.93e-01 |
| G alpha (z) signalling events | 41 | 9.84e-01 | 0.001860 | 9.93e-01 |
| IRS-mediated signalling | 45 | 9.85e-01 | -0.001570 | 9.93e-01 |
| Interleukin-4 and Interleukin-13 signaling | 105 | 9.80e-01 | 0.001430 | 9.93e-01 |
| FCGR3A-mediated phagocytosis | 64 | 9.85e-01 | -0.001360 | 9.93e-01 |
| Leishmania phagocytosis | 64 | 9.85e-01 | -0.001360 | 9.93e-01 |
| Parasite infection | 64 | 9.85e-01 | -0.001360 | 9.93e-01 |
| RAB GEFs exchange GTP for GDP on RABs | 80 | 9.85e-01 | -0.001230 | 9.93e-01 |
| Signaling by high-kinase activity BRAF mutants | 33 | 9.91e-01 | 0.001140 | 9.98e-01 |
| Nuclear Events (kinase and transcription factor activation) | 61 | 9.95e-01 | -0.000492 | 9.99e-01 |
| RAB geranylgeranylation | 54 | 9.96e-01 | 0.000401 | 9.99e-01 |
| Class A/1 (Rhodopsin-like receptors) | 288 | 9.92e-01 | 0.000324 | 9.99e-01 |
| Diseases associated with visual transduction | 11 | 9.99e-01 | -0.000295 | 9.99e-01 |
| Diseases of the neuronal system | 11 | 9.99e-01 | -0.000295 | 9.99e-01 |
| Retinoid cycle disease events | 11 | 9.99e-01 | -0.000295 | 9.99e-01 |
| Adenylate cyclase activating pathway | 10 | 9.99e-01 | 0.000220 | 9.99e-01 |
| Energy dependent regulation of mTOR by LKB1-AMPK | 25 | 9.99e-01 | -0.000203 | 9.99e-01 |
| Na+/Cl- dependent neurotransmitter transporters | 17 | 9.99e-01 | 0.000176 | 9.99e-01 |
| Interferon Signaling | 150 | 9.98e-01 | -0.000148 | 9.99e-01 |
Olfactory Signaling Pathway
| 775 | |
|---|---|
| set | Olfactory Signaling Pathway |
| setSize | 279 |
| pANOVA | 4.49e-71 |
| s.dist | 0.619 |
| p.adjustANOVA | 6.25e-68 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| OR5P2 | 7120.0 |
| OR4C15 | 7094.0 |
| OR2AG1 | 7092.5 |
| OR2AG2 | 7092.5 |
| OR1E1 | 7090.5 |
| OR1E2 | 7090.5 |
| OR5B3 | 7089.0 |
| OR4A16 | 7082.5 |
| OR4A5 | 7082.5 |
| OR5W2 | 7071.0 |
| OR8K3 | 7070.0 |
| OR7G2 | 7043.0 |
| OR8K5 | 7042.0 |
| OR14A2 | 7039.0 |
| OR7E24 | 7031.0 |
| OR5AN1 | 7030.0 |
| OR10A3 | 7023.5 |
| OR10A6 | 7023.5 |
| OR8H1 | 7021.0 |
| OR8H2 | 7021.0 |
| GeneID | Gene Rank |
|---|---|
| OR5P2 | 7120.0 |
| OR4C15 | 7094.0 |
| OR2AG1 | 7092.5 |
| OR2AG2 | 7092.5 |
| OR1E1 | 7090.5 |
| OR1E2 | 7090.5 |
| OR5B3 | 7089.0 |
| OR4A16 | 7082.5 |
| OR4A5 | 7082.5 |
| OR5W2 | 7071.0 |
| OR8K3 | 7070.0 |
| OR7G2 | 7043.0 |
| OR8K5 | 7042.0 |
| OR14A2 | 7039.0 |
| OR7E24 | 7031.0 |
| OR5AN1 | 7030.0 |
| OR10A3 | 7023.5 |
| OR10A6 | 7023.5 |
| OR8H1 | 7021.0 |
| OR8H2 | 7021.0 |
| OR8H3 | 7021.0 |
| OR7D4 | 7015.0 |
| OR4C16 | 7013.0 |
| OR5T2 | 7005.0 |
| OR8D1 | 7004.0 |
| OR52N2 | 7003.0 |
| OR9G1 | 7002.0 |
| OR2AJ1 | 6991.0 |
| OR8B2 | 6989.5 |
| OR8B3 | 6989.5 |
| OR5T1 | 6985.5 |
| OR5T3 | 6985.5 |
| OR52R1 | 6983.0 |
| OR5K4 | 6978.0 |
| OR9I1 | 6975.0 |
| OR4K15 | 6972.0 |
| OR4C12 | 6971.0 |
| OR4D10 | 6969.0 |
| OR5D18 | 6957.0 |
| OR4C11 | 6955.0 |
| OR8B12 | 6947.0 |
| OR52A5 | 6945.0 |
| OR10AG1 | 6941.0 |
| OR2A1 | 6937.5 |
| OR4L1 | 6934.0 |
| OR2F1 | 6932.5 |
| OR2F2 | 6932.5 |
| OR2A14 | 6930.0 |
| OR2T29 | 6928.0 |
| OR2T4 | 6928.0 |
| OR2T5 | 6928.0 |
| OR4B1 | 6919.0 |
| OR6C1 | 6914.0 |
| OR5D14 | 6913.0 |
| OR4N4 | 6912.0 |
| OR10J3 | 6892.5 |
| OR10J4 | 6892.5 |
| OR5M11 | 6889.0 |
| OR6C76 | 6882.0 |
| OR13G1 | 6879.0 |
| OR6C70 | 6878.0 |
| OR6C6 | 6877.0 |
| OR5V1 | 6871.0 |
| OR5P3 | 6867.0 |
| OR1N1 | 6851.0 |
| OR8D2 | 6840.0 |
| OR5AK2 | 6824.0 |
| OR8I2 | 6815.0 |
| OR5M1 | 6804.5 |
| OR5M10 | 6804.5 |
| OR1A1 | 6800.0 |
| OR9K2 | 6789.0 |
| OR11H4 | 6734.0 |
| OR5B12 | 6722.0 |
| OR4A47 | 6715.0 |
| OR56A4 | 6705.0 |
| OR4K2 | 6692.0 |
| OR3A1 | 6691.0 |
| OR5AP2 | 6677.0 |
| OR2W1 | 6656.0 |
| OR4X2 | 6591.0 |
| OR1S1 | 6553.5 |
| OR1S2 | 6553.5 |
| OR10A2 | 6549.5 |
| OR10A5 | 6549.5 |
| OR6F1 | 6548.0 |
| OR51A7 | 6529.0 |
| OR6C3 | 6528.0 |
| OR2AP1 | 6510.0 |
| OR4P4 | 6488.0 |
| OR56B1 | 6480.0 |
| OR10X1 | 6479.0 |
| OR6C75 | 6475.0 |
| OR4F15 | 6452.0 |
| OR14J1 | 6443.0 |
| OR5AS1 | 6413.0 |
| OR8B4 | 6394.0 |
| OR11A1 | 6392.0 |
| OR5M3 | 6356.0 |
| OR8B8 | 6331.0 |
| OR2A12 | 6322.0 |
| OR8J1 | 6315.5 |
| OR8J3 | 6315.5 |
| OR2T2 | 6267.5 |
| OR2T35 | 6267.5 |
| OR12D2 | 6262.5 |
| OR51F1 | 6261.0 |
| OR4K1 | 6257.0 |
| OR5B2 | 6193.0 |
| OR1C1 | 6188.0 |
| OR2V2 | 6187.0 |
| OR1Q1 | 6179.0 |
| OR5B21 | 6176.0 |
| OR5D16 | 6167.0 |
| OR4K5 | 6136.0 |
| OR5M8 | 6112.0 |
| OR10Q1 | 6104.0 |
| OR8A1 | 6102.0 |
| OR51E2 | 6091.0 |
| OR4N5 | 6079.0 |
| OR51G2 | 6041.0 |
| OR4C5 | 5984.0 |
| OR51Q1 | 5960.0 |
| OR6N1 | 5891.0 |
| OR11H7 | 5845.0 |
| OR6K6 | 5804.0 |
| OR6N2 | 5788.0 |
| OR6C65 | 5699.0 |
| OR10G4 | 5629.5 |
| OR10G7 | 5629.5 |
| OR10G8 | 5629.5 |
| OR10G9 | 5629.5 |
| OR1L4 | 5589.5 |
| OR1L6 | 5589.5 |
| OR6C68 | 5541.0 |
| OR1L8 | 5536.0 |
| OR10J5 | 5494.0 |
| OR10H1 | 5448.0 |
| OR10H2 | 5448.0 |
| OR10H5 | 5448.0 |
| OR1F1 | 5427.0 |
| GNGT1 | 5409.0 |
| OR6C2 | 5401.0 |
| OR9G4 | 5397.0 |
| OR52E6 | 5339.5 |
| OR52E8 | 5339.5 |
| OR1J1 | 5325.0 |
| OR9Q1 | 5316.0 |
| OR52N5 | 5310.0 |
| OR6K3 | 5228.0 |
| OR9Q2 | 5193.0 |
| OR10D3 | 5138.0 |
| OR10J1 | 5084.0 |
| OR13A1 | 5049.0 |
| OR1M1 | 5040.0 |
| OR4F17 | 5020.0 |
| OR4F4 | 5020.0 |
| OR4F5 | 5020.0 |
| OR10G2 | 4978.0 |
| OR8K1 | 4863.0 |
| OR11H6 | 4806.0 |
| OR2J1 | 4793.5 |
| OR2J2 | 4793.5 |
| OR10P1 | 4744.0 |
| OR13H1 | 4690.0 |
| OR2AK2 | 4678.0 |
| OR5L1 | 4674.5 |
| OR5L2 | 4674.5 |
| OR13C8 | 4624.0 |
| OR2D2 | 4587.0 |
| OR51F2 | 4473.0 |
| OR5AR1 | 4468.0 |
| OR6C74 | 4258.0 |
| OR2A5 | 4176.0 |
| OR52E2 | 4154.0 |
| OR5J2 | 4065.0 |
| OR2L2 | 4044.5 |
| OR2L3 | 4044.5 |
| OR2L5 | 4044.5 |
| OR2L8 | 4044.5 |
| OR51B4 | 4039.0 |
| REEP5 | 4002.0 |
| OR13F1 | 3879.0 |
| OR4D11 | 3827.0 |
| OR52I1 | 3825.5 |
| OR52I2 | 3825.5 |
| OR2K2 | 3822.0 |
| OR2D3 | 3806.0 |
| OR52J3 | 3782.0 |
| OR4Q3 | 3625.0 |
| OR51I2 | 3608.0 |
| OR10W1 | 3576.0 |
| OR5A2 | 3479.0 |
| OR2A2 | 3405.0 |
| OR2A4 | 3400.5 |
| OR2A7 | 3400.5 |
| OR2A25 | 3279.0 |
| OR5I1 | 3155.0 |
| OR10V1 | 3147.0 |
| OR2T6 | 3122.0 |
| OR51S1 | 3112.0 |
| OR8U1 | 2997.0 |
| OR1I1 | 2950.0 |
| OR8D4 | 2945.0 |
| OR4M1 | 2797.5 |
| OR4M2 | 2797.5 |
| OR12D3 | 2755.0 |
| OR4A15 | 2744.0 |
| RTP4 | 2690.0 |
| OR7C2 | 2505.0 |
| OR51T1 | 2455.0 |
| REEP1 | 2363.0 |
| OR51G1 | 2281.0 |
| OR51I1 | 2222.0 |
| OR4S2 | 2172.0 |
| OR9A4 | 2098.0 |
| OR13D1 | 2086.0 |
| OR10A4 | 2023.0 |
| OR9A2 | 1784.0 |
| OR6B1 | 1667.0 |
| OR10C1 | 1665.0 |
| OR52W1 | 1586.0 |
| OR10K2 | 1517.0 |
| OR10H3 | 1513.5 |
| OR10H4 | 1513.5 |
| OR10Z1 | 1476.0 |
| OR13C3 | 1390.0 |
| OR6A2 | 1363.0 |
| OR6P1 | 1290.0 |
| OR4D6 | 1175.0 |
| OR52E4 | 943.0 |
| RTP3 | 878.0 |
| OR52L1 | 821.0 |
| GNB1 | 691.0 |
| OR1J4 | 626.0 |
| OR51M1 | 493.0 |
| OR6Y1 | 445.0 |
| OR6X1 | 421.0 |
| OR4D5 | 390.0 |
| OR2C1 | 240.0 |
| OR51E1 | -6.0 |
| OR2T1 | -117.0 |
| OR6K2 | -288.0 |
| OR4C3 | -321.0 |
| OR5C1 | -642.0 |
| OR52M1 | -759.0 |
| OR5A1 | -933.0 |
| OR4E2 | -1509.0 |
| OR52B2 | -1744.0 |
| REEP6 | -2376.0 |
| OR2B6 | -2507.0 |
| GNAL | -2784.0 |
| OR10S1 | -3125.0 |
| OR51D1 | -3482.0 |
| OR2B11 | -3547.0 |
| OR4D1 | -3775.0 |
| OR6B2 | -3909.5 |
| OR6B3 | -3909.5 |
| OR52K2 | -3928.0 |
| OR7G3 | -3992.0 |
| OR52H1 | -4185.0 |
| OR2AT4 | -4534.0 |
| OR5AU1 | -5169.0 |
| RTP1 | -5259.0 |
| RTP2 | -5372.0 |
| OR10AD1 | -5541.0 |
| OR2T12 | -6036.0 |
| OR2T33 | -6036.0 |
| OR2T8 | -6036.0 |
| OR52N4 | -6095.0 |
| OR6S1 | -6232.0 |
| OR13J1 | -6384.0 |
| OR52D1 | -6603.0 |
| REEP2 | -6911.0 |
| OR11L1 | -6953.0 |
| REEP4 | -7744.0 |
| OR2W3 | -8042.0 |
| OR10G3 | -8743.0 |
| OR4D2 | -8795.0 |
Glucuronidation
| 469 | |
|---|---|
| set | Glucuronidation |
| setSize | 17 |
| pANOVA | 0.000153 |
| s.dist | 0.53 |
| p.adjustANOVA | 0.0233 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UGT2A1 | 6946.0 |
| UGT1A10 | 6902.5 |
| UGT1A7 | 6902.5 |
| UGT1A8 | 6902.5 |
| UGT1A9 | 6902.5 |
| UGP2 | 6147.0 |
| ABHD10 | 4873.0 |
| UGT1A6 | 3489.0 |
| UGT1A3 | 3139.0 |
| UGT1A4 | 3139.0 |
| UGT1A5 | 3139.0 |
| SLC35D1 | 2383.0 |
| UGT3A1 | 1563.5 |
| UGT3A2 | 1563.5 |
| UGT2A3 | 800.0 |
| UGT1A1 | -1211.0 |
| UGDH | -7867.0 |
| GeneID | Gene Rank |
|---|---|
| UGT2A1 | 6946.0 |
| UGT1A10 | 6902.5 |
| UGT1A7 | 6902.5 |
| UGT1A8 | 6902.5 |
| UGT1A9 | 6902.5 |
| UGP2 | 6147.0 |
| ABHD10 | 4873.0 |
| UGT1A6 | 3489.0 |
| UGT1A3 | 3139.0 |
| UGT1A4 | 3139.0 |
| UGT1A5 | 3139.0 |
| SLC35D1 | 2383.0 |
| UGT3A1 | 1563.5 |
| UGT3A2 | 1563.5 |
| UGT2A3 | 800.0 |
| UGT1A1 | -1211.0 |
| UGDH | -7867.0 |
Passive transport by Aquaporins
| 820 | |
|---|---|
| set | Passive transport by Aquaporins |
| setSize | 12 |
| pANOVA | 0.0046 |
| s.dist | -0.472 |
| p.adjustANOVA | 0.297 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| AQP6 | -8056.0 |
| AQP7 | -7985.0 |
| AQP12A | -7323.5 |
| AQP5 | -6991.0 |
| AQP3 | -6778.0 |
| AQP2 | -6548.0 |
| MIP | -6512.0 |
| AQP11 | -4084.0 |
| AQP8 | -3967.0 |
| AQP9 | -2696.0 |
| AQP1 | -2564.0 |
| AQP4 | 4553.0 |
| GeneID | Gene Rank |
|---|---|
| AQP6 | -8056.0 |
| AQP7 | -7985.0 |
| AQP12A | -7323.5 |
| AQP5 | -6991.0 |
| AQP3 | -6778.0 |
| AQP2 | -6548.0 |
| MIP | -6512.0 |
| AQP11 | -4084.0 |
| AQP8 | -3967.0 |
| AQP9 | -2696.0 |
| AQP1 | -2564.0 |
| AQP4 | 4553.0 |
TRAF6 mediated IRF7 activation
| 1238 | |
|---|---|
| set | TRAF6 mediated IRF7 activation |
| setSize | 28 |
| pANOVA | 2.21e-05 |
| s.dist | 0.463 |
| p.adjustANOVA | 0.00385 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IFNA1 | 7051 |
| IFNA10 | 7051 |
| IFNA14 | 7051 |
| IFNA16 | 7051 |
| IFNA17 | 7051 |
| IFNA2 | 7051 |
| IFNA21 | 7051 |
| IFNA4 | 7051 |
| IFNA5 | 7051 |
| IFNA6 | 7051 |
| IFNA7 | 7051 |
| IFNA8 | 7051 |
| TANK | 6503 |
| IFNB1 | 5508 |
| SIKE1 | 4119 |
| TRAF6 | 3268 |
| IFIH1 | 2897 |
| EP300 | 1892 |
| CREBBP | 1152 |
| TRAF2 | 81 |
| GeneID | Gene Rank |
|---|---|
| IFNA1 | 7051 |
| IFNA10 | 7051 |
| IFNA14 | 7051 |
| IFNA16 | 7051 |
| IFNA17 | 7051 |
| IFNA2 | 7051 |
| IFNA21 | 7051 |
| IFNA4 | 7051 |
| IFNA5 | 7051 |
| IFNA6 | 7051 |
| IFNA7 | 7051 |
| IFNA8 | 7051 |
| TANK | 6503 |
| IFNB1 | 5508 |
| SIKE1 | 4119 |
| TRAF6 | 3268 |
| IFIH1 | 2897 |
| EP300 | 1892 |
| CREBBP | 1152 |
| TRAF2 | 81 |
| MAVS | -1815 |
| IRF7 | -1820 |
| RNF135 | -1885 |
| TRIM25 | -2820 |
| TBK1 | -5984 |
| IRF3 | -6107 |
| DDX58 | -6505 |
| IKBKE | -6765 |
G alpha (s) signalling events
| 417 | |
|---|---|
| set | G alpha (s) signalling events |
| setSize | 408 |
| pANOVA | 4.62e-50 |
| s.dist | 0.429 |
| p.adjustANOVA | 3.21e-47 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| OR5P2 | 7120.0 |
| OR4C15 | 7094.0 |
| OR2AG1 | 7092.5 |
| OR2AG2 | 7092.5 |
| OR1E1 | 7090.5 |
| OR1E2 | 7090.5 |
| OR5B3 | 7089.0 |
| OR4A16 | 7082.5 |
| OR4A5 | 7082.5 |
| OR5W2 | 7071.0 |
| OR8K3 | 7070.0 |
| OR7G2 | 7043.0 |
| OR8K5 | 7042.0 |
| OR14A2 | 7039.0 |
| OR7E24 | 7031.0 |
| OR5AN1 | 7030.0 |
| OR10A3 | 7023.5 |
| OR10A6 | 7023.5 |
| OR8H1 | 7021.0 |
| OR8H2 | 7021.0 |
| GeneID | Gene Rank |
|---|---|
| OR5P2 | 7120.0 |
| OR4C15 | 7094.0 |
| OR2AG1 | 7092.5 |
| OR2AG2 | 7092.5 |
| OR1E1 | 7090.5 |
| OR1E2 | 7090.5 |
| OR5B3 | 7089.0 |
| OR4A16 | 7082.5 |
| OR4A5 | 7082.5 |
| OR5W2 | 7071.0 |
| OR8K3 | 7070.0 |
| OR7G2 | 7043.0 |
| OR8K5 | 7042.0 |
| OR14A2 | 7039.0 |
| OR7E24 | 7031.0 |
| OR5AN1 | 7030.0 |
| OR10A3 | 7023.5 |
| OR10A6 | 7023.5 |
| OR8H1 | 7021.0 |
| OR8H2 | 7021.0 |
| OR8H3 | 7021.0 |
| OR7D4 | 7015.0 |
| OR4C16 | 7013.0 |
| OR5T2 | 7005.0 |
| OR8D1 | 7004.0 |
| OR52N2 | 7003.0 |
| OR9G1 | 7002.0 |
| OR2AJ1 | 6991.0 |
| OR8B2 | 6989.5 |
| OR8B3 | 6989.5 |
| OR5T1 | 6985.5 |
| OR5T3 | 6985.5 |
| OR52R1 | 6983.0 |
| OR5K4 | 6978.0 |
| OR9I1 | 6975.0 |
| OR4K15 | 6972.0 |
| OR4C12 | 6971.0 |
| OR4D10 | 6969.0 |
| OR5D18 | 6957.0 |
| OR4C11 | 6955.0 |
| OR8B12 | 6947.0 |
| OR52A5 | 6945.0 |
| OR10AG1 | 6941.0 |
| OR2A1 | 6937.5 |
| OR4L1 | 6934.0 |
| OR2F1 | 6932.5 |
| OR2F2 | 6932.5 |
| OR2A14 | 6930.0 |
| OR2T29 | 6928.0 |
| OR2T4 | 6928.0 |
| OR2T5 | 6928.0 |
| OR4B1 | 6919.0 |
| OR6C1 | 6914.0 |
| OR5D14 | 6913.0 |
| OR4N4 | 6912.0 |
| OR10J3 | 6892.5 |
| OR10J4 | 6892.5 |
| OR5M11 | 6889.0 |
| OR6C76 | 6882.0 |
| OR13G1 | 6879.0 |
| OR6C70 | 6878.0 |
| OR6C6 | 6877.0 |
| OR5V1 | 6871.0 |
| OR5P3 | 6867.0 |
| OR1N1 | 6851.0 |
| OR8D2 | 6840.0 |
| OR5AK2 | 6824.0 |
| OR8I2 | 6815.0 |
| OR5M1 | 6804.5 |
| OR5M10 | 6804.5 |
| OR1A1 | 6800.0 |
| OR9K2 | 6789.0 |
| PDE3B | 6785.0 |
| OR11H4 | 6734.0 |
| OR5B12 | 6722.0 |
| OR4A47 | 6715.0 |
| OR56A4 | 6705.0 |
| OR4K2 | 6692.0 |
| OR3A1 | 6691.0 |
| OR5AP2 | 6677.0 |
| CALCR | 6675.0 |
| OR2W1 | 6656.0 |
| OR4X2 | 6591.0 |
| OR1S1 | 6553.5 |
| OR1S2 | 6553.5 |
| OR10A2 | 6549.5 |
| OR10A5 | 6549.5 |
| OR6F1 | 6548.0 |
| OR51A7 | 6529.0 |
| OR6C3 | 6528.0 |
| OR2AP1 | 6510.0 |
| OR4P4 | 6488.0 |
| OR56B1 | 6480.0 |
| OR10X1 | 6479.0 |
| OR6C75 | 6475.0 |
| OR4F15 | 6452.0 |
| OR14J1 | 6443.0 |
| OR5AS1 | 6413.0 |
| OR8B4 | 6394.0 |
| OR11A1 | 6392.0 |
| OR5M3 | 6356.0 |
| OR8B8 | 6331.0 |
| OR2A12 | 6322.0 |
| OR8J1 | 6315.5 |
| OR8J3 | 6315.5 |
| OR2T2 | 6267.5 |
| OR2T35 | 6267.5 |
| OR12D2 | 6262.5 |
| OR51F1 | 6261.0 |
| OR4K1 | 6257.0 |
| OR5B2 | 6193.0 |
| OR1C1 | 6188.0 |
| OR2V2 | 6187.0 |
| OR1Q1 | 6179.0 |
| OR5B21 | 6176.0 |
| OR5D16 | 6167.0 |
| OR4K5 | 6136.0 |
| OR5M8 | 6112.0 |
| OR10Q1 | 6104.0 |
| OR8A1 | 6102.0 |
| ADCYAP1 | 6097.0 |
| OR51E2 | 6091.0 |
| OR4N5 | 6079.0 |
| OR51G2 | 6041.0 |
| OR4C5 | 5984.0 |
| PDE7A | 5973.0 |
| GNG11 | 5968.0 |
| OR51Q1 | 5960.0 |
| OR6N1 | 5891.0 |
| OR11H7 | 5845.0 |
| GPR150 | 5834.0 |
| PTGER2 | 5815.0 |
| OR6K6 | 5804.0 |
| OR6N2 | 5788.0 |
| CALCRL | 5768.0 |
| OR6C65 | 5699.0 |
| OR10G4 | 5629.5 |
| OR10G7 | 5629.5 |
| OR10G8 | 5629.5 |
| OR10G9 | 5629.5 |
| OR1L4 | 5589.5 |
| OR1L6 | 5589.5 |
| PTH2R | 5582.0 |
| OR6C68 | 5541.0 |
| OR1L8 | 5536.0 |
| OR10J5 | 5494.0 |
| PDE1A | 5462.0 |
| OR10H1 | 5448.0 |
| OR10H2 | 5448.0 |
| OR10H5 | 5448.0 |
| OR1F1 | 5427.0 |
| GNGT1 | 5409.0 |
| OR6C2 | 5401.0 |
| OR9G4 | 5397.0 |
| GNAT3 | 5366.0 |
| OR52E6 | 5339.5 |
| OR52E8 | 5339.5 |
| OR1J1 | 5325.0 |
| OR9Q1 | 5316.0 |
| OR52N5 | 5310.0 |
| OR6K3 | 5228.0 |
| OR9Q2 | 5193.0 |
| OR10D3 | 5138.0 |
| OR10J1 | 5084.0 |
| CRH | 5077.0 |
| OR13A1 | 5049.0 |
| OR1M1 | 5040.0 |
| OR4F17 | 5020.0 |
| OR4F4 | 5020.0 |
| OR4F5 | 5020.0 |
| OR10G2 | 4978.0 |
| ADCY2 | 4943.0 |
| OR8K1 | 4863.0 |
| OR11H6 | 4806.0 |
| OR2J1 | 4793.5 |
| OR2J2 | 4793.5 |
| CALCA | 4781.0 |
| OR10P1 | 4744.0 |
| OR13H1 | 4690.0 |
| OR2AK2 | 4678.0 |
| OR5L1 | 4674.5 |
| OR5L2 | 4674.5 |
| OR13C8 | 4624.0 |
| PDE4D | 4590.0 |
| OR2D2 | 4587.0 |
| TAAR8 | 4567.0 |
| GNAI3 | 4522.0 |
| PTH | 4515.0 |
| OR51F2 | 4473.0 |
| OR5AR1 | 4468.0 |
| GNAI1 | 4379.0 |
| NPSR1 | 4313.0 |
| OR6C74 | 4258.0 |
| ADCY8 | 4229.0 |
| ADCY1 | 4198.0 |
| OR2A5 | 4176.0 |
| OR52E2 | 4154.0 |
| OR5J2 | 4065.0 |
| OR2L2 | 4044.5 |
| OR2L3 | 4044.5 |
| OR2L5 | 4044.5 |
| OR2L8 | 4044.5 |
| OR51B4 | 4039.0 |
| REEP5 | 4002.0 |
| PTGER4 | 3882.0 |
| OR13F1 | 3879.0 |
| LHCGR | 3840.0 |
| GRK6 | 3834.0 |
| OR4D11 | 3827.0 |
| OR52I1 | 3825.5 |
| OR52I2 | 3825.5 |
| OR2K2 | 3822.0 |
| OR2D3 | 3806.0 |
| OR52J3 | 3782.0 |
| GNG2 | 3663.0 |
| OR4Q3 | 3625.0 |
| OR51I2 | 3608.0 |
| GNG4 | 3607.0 |
| OR10W1 | 3576.0 |
| RAMP2 | 3512.0 |
| GRK5 | 3504.0 |
| OR5A2 | 3479.0 |
| CYSLTR2 | 3448.0 |
| TAAR1 | 3423.0 |
| OR2A2 | 3405.0 |
| OR2A4 | 3400.5 |
| OR2A7 | 3400.5 |
| ADORA2A | 3386.0 |
| GCG | 3328.0 |
| OR2A25 | 3279.0 |
| TSHB | 3252.0 |
| OR5I1 | 3155.0 |
| OR10V1 | 3147.0 |
| OR2T6 | 3122.0 |
| OR51S1 | 3112.0 |
| PDE8A | 3099.0 |
| OR8U1 | 2997.0 |
| PDE7B | 2971.0 |
| OR1I1 | 2950.0 |
| OR8D4 | 2945.0 |
| DRD5 | 2812.0 |
| OR4M1 | 2797.5 |
| OR4M2 | 2797.5 |
| OR12D3 | 2755.0 |
| OR4A15 | 2744.0 |
| HTR7 | 2723.0 |
| IAPP | 2693.0 |
| RTP4 | 2690.0 |
| RXFP1 | 2664.0 |
| OR7C2 | 2505.0 |
| OR51T1 | 2455.0 |
| REEP1 | 2363.0 |
| CALCB | 2311.0 |
| OR51G1 | 2281.0 |
| PTHLH | 2270.0 |
| ADCY4 | 2226.0 |
| OR51I1 | 2222.0 |
| OR4S2 | 2172.0 |
| OR9A4 | 2098.0 |
| OR13D1 | 2086.0 |
| OR10A4 | 2023.0 |
| VIP | 1879.0 |
| PDE1B | 1796.0 |
| OR9A2 | 1784.0 |
| OR6B1 | 1667.0 |
| OR10C1 | 1665.0 |
| VIPR2 | 1599.0 |
| OR52W1 | 1586.0 |
| FSHB | 1532.0 |
| OR10K2 | 1517.0 |
| OR10H3 | 1513.5 |
| OR10H4 | 1513.5 |
| OR10Z1 | 1476.0 |
| OR13C3 | 1390.0 |
| OR6A2 | 1363.0 |
| OR6P1 | 1290.0 |
| OR4D6 | 1175.0 |
| GNAI2 | 1164.0 |
| ADRB2 | 1072.0 |
| OR52E4 | 943.0 |
| RTP3 | 878.0 |
| OR52L1 | 821.0 |
| ADCY9 | 745.0 |
| GNB1 | 691.0 |
| OR1J4 | 626.0 |
| TAAR6 | 501.0 |
| OR51M1 | 493.0 |
| OR6Y1 | 445.0 |
| TAAR9 | 439.0 |
| OR6X1 | 421.0 |
| OR4D5 | 390.0 |
| GPR15 | 283.0 |
| PDE3A | 271.0 |
| OR2C1 | 240.0 |
| OR51E1 | -6.0 |
| OR2T1 | -117.0 |
| POMC | -215.0 |
| OR6K2 | -288.0 |
| OR4C3 | -321.0 |
| PTH2 | -406.0 |
| FSHR | -432.0 |
| MC4R | -458.0 |
| OR5C1 | -642.0 |
| OR52M1 | -759.0 |
| OR5A1 | -933.0 |
| GPR27 | -936.0 |
| GIPR | -965.0 |
| NPS | -978.0 |
| TAAR2 | -1188.0 |
| HRH2 | -1227.0 |
| TAAR5 | -1488.0 |
| OR4E2 | -1509.0 |
| GPR25 | -1556.0 |
| MC2R | -1573.0 |
| TSHR | -1606.0 |
| OR52B2 | -1744.0 |
| CRHR2 | -1834.0 |
| GPR176 | -1877.0 |
| ADRB1 | -1929.0 |
| GLP1R | -2167.0 |
| GPBAR1 | -2187.0 |
| PDE8B | -2240.0 |
| CRHR1 | -2254.0 |
| GNG8 | -2264.0 |
| SCTR | -2267.0 |
| REEP6 | -2376.0 |
| OR2B6 | -2507.0 |
| ARRB2 | -2547.0 |
| HTR4 | -2719.0 |
| GNAL | -2784.0 |
| RLN2 | -2852.5 |
| GPR45 | -2863.0 |
| ADRB3 | -2867.0 |
| GNG10 | -3056.0 |
| OR10S1 | -3125.0 |
| ADCY6 | -3142.0 |
| GNG13 | -3237.0 |
| RLN3 | -3256.0 |
| GNB4 | -3321.0 |
| GLP2R | -3346.0 |
| OR51D1 | -3482.0 |
| RAMP1 | -3522.0 |
| OR2B11 | -3547.0 |
| CGA | -3665.0 |
| OR4D1 | -3775.0 |
| GHRHR | -3813.0 |
| ADCY5 | -3841.0 |
| OR6B2 | -3909.5 |
| OR6B3 | -3909.5 |
| OR52K2 | -3928.0 |
| AVP | -3990.0 |
| OR7G3 | -3992.0 |
| OR52H1 | -4185.0 |
| PDE11A | -4205.0 |
| ADORA2B | -4228.0 |
| ADCYAP1R1 | -4238.0 |
| OR2AT4 | -4534.0 |
| GPR20 | -4545.0 |
| PDE2A | -4578.0 |
| DRD1 | -4585.0 |
| SCT | -4622.0 |
| PTH1R | -4720.0 |
| AVPR2 | -4747.0 |
| ARRB1 | -4917.0 |
| ADM | -5101.0 |
| OR5AU1 | -5169.0 |
| GPR83 | -5187.0 |
| RTP1 | -5259.0 |
| GPR84 | -5335.0 |
| RTP2 | -5372.0 |
| GPR39 | -5390.0 |
| MC5R | -5505.0 |
| OR10AD1 | -5541.0 |
| INSL3 | -5599.0 |
| GNB5 | -5643.0 |
| MC1R | -5805.0 |
| OR2T12 | -6036.0 |
| OR2T33 | -6036.0 |
| OR2T8 | -6036.0 |
| OR52N4 | -6095.0 |
| OR6S1 | -6232.0 |
| OR13J1 | -6384.0 |
| MC3R | -6577.0 |
| OR52D1 | -6603.0 |
| GNAS | -6635.0 |
| GIP | -6657.0 |
| HTR6 | -6826.0 |
| VIPR1 | -6828.0 |
| REEP2 | -6911.0 |
| OR11L1 | -6953.0 |
| GHRH | -7284.0 |
| ADM2 | -7458.0 |
| PDE10A | -7478.0 |
| SRC | -7505.0 |
| REEP4 | -7744.0 |
| GNB3 | -7843.0 |
| RXFP2 | -7938.0 |
| GNG7 | -7958.0 |
| GNAZ | -7968.0 |
| OR2W3 | -8042.0 |
| GPHA2 | -8107.0 |
| ADCY7 | -8353.0 |
| ADCY3 | -8738.0 |
| OR10G3 | -8743.0 |
| PTGIR | -8769.0 |
| OR4D2 | -8795.0 |
| PDE4A | -8849.0 |
| PDE4C | -8955.0 |
Class C/3 (Metabotropic glutamate/pheromone receptors)
| 193 | |
|---|---|
| set | Class C/3 (Metabotropic glutamate/pheromone receptors) |
| setSize | 34 |
| pANOVA | 1.62e-05 |
| s.dist | 0.427 |
| p.adjustANOVA | 0.00321 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TAS2R14 | 7088 |
| TAS2R13 | 7012 |
| TAS2R19 | 6908 |
| TAS2R20 | 6908 |
| TAS2R30 | 6908 |
| TAS2R31 | 6908 |
| TAS2R43 | 6908 |
| TAS2R46 | 6908 |
| TAS2R50 | 6908 |
| GRM3 | 6777 |
| GRM5 | 6735 |
| TAS2R10 | 6231 |
| GRM8 | 5703 |
| GRM7 | 5642 |
| GPRC6A | 5581 |
| TAS2R1 | 5209 |
| TAS2R3 | 4645 |
| TAS2R42 | 4527 |
| TAS2R16 | 3983 |
| TAS2R41 | 3870 |
| GeneID | Gene Rank |
|---|---|
| TAS2R14 | 7088 |
| TAS2R13 | 7012 |
| TAS2R19 | 6908 |
| TAS2R20 | 6908 |
| TAS2R30 | 6908 |
| TAS2R31 | 6908 |
| TAS2R43 | 6908 |
| TAS2R46 | 6908 |
| TAS2R50 | 6908 |
| GRM3 | 6777 |
| GRM5 | 6735 |
| TAS2R10 | 6231 |
| GRM8 | 5703 |
| GRM7 | 5642 |
| GPRC6A | 5581 |
| TAS2R1 | 5209 |
| TAS2R3 | 4645 |
| TAS2R42 | 4527 |
| TAS2R16 | 3983 |
| TAS2R41 | 3870 |
| TAS2R38 | 3839 |
| TAS2R7 | 3291 |
| TAS2R60 | 3091 |
| TAS2R39 | 2388 |
| GRM1 | 409 |
| TAS2R40 | -1608 |
| CASR | -2774 |
| GABBR2 | -3012 |
| TAS1R3 | -5258 |
| GRM6 | -6274 |
| TAS1R2 | -7810 |
| GRM4 | -7906 |
| GABBR1 | -8250 |
| GRM2 | -8786 |
PI3K events in ERBB4 signaling
| 802 | |
|---|---|
| set | PI3K events in ERBB4 signaling |
| setSize | 10 |
| pANOVA | 0.0204 |
| s.dist | 0.423 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ERBB4 | 6841 |
| NRG1 | 5376 |
| NRG3 | 5354 |
| EREG | 3888 |
| PIK3R1 | 3668 |
| BTC | 3507 |
| NRG4 | 755 |
| NRG2 | -1156 |
| HBEGF | -1977 |
| PIK3CA | -2203 |
| GeneID | Gene Rank |
|---|---|
| ERBB4 | 6841 |
| NRG1 | 5376 |
| NRG3 | 5354 |
| EREG | 3888 |
| PIK3R1 | 3668 |
| BTC | 3507 |
| NRG4 | 755 |
| NRG2 | -1156 |
| HBEGF | -1977 |
| PIK3CA | -2203 |
Removal of the Flap Intermediate
| 1017 | |
|---|---|
| set | Removal of the Flap Intermediate |
| setSize | 11 |
| pANOVA | 0.016 |
| s.dist | -0.419 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLD1 | -9075 |
| DNA2 | -8862 |
| POLD2 | -8726 |
| RPA2 | -8622 |
| PRIM1 | -7779 |
| POLA2 | -5833 |
| PCNA | -5055 |
| RPA1 | -1771 |
| PRIM2 | -50 |
| POLD3 | 1469 |
| POLA1 | 5038 |
| GeneID | Gene Rank |
|---|---|
| POLD1 | -9075 |
| DNA2 | -8862 |
| POLD2 | -8726 |
| RPA2 | -8622 |
| PRIM1 | -7779 |
| POLA2 | -5833 |
| PCNA | -5055 |
| RPA1 | -1771 |
| PRIM2 | -50 |
| POLD3 | 1469 |
| POLA1 | 5038 |
SHC1 events in ERBB4 signaling
| 1058 | |
|---|---|
| set | SHC1 events in ERBB4 signaling |
| setSize | 14 |
| pANOVA | 0.00762 |
| s.dist | 0.412 |
| p.adjustANOVA | 0.374 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ERBB4 | 6841 |
| NRAS | 5491 |
| NRG1 | 5376 |
| NRG3 | 5354 |
| KRAS | 4959 |
| EREG | 3888 |
| BTC | 3507 |
| GRB2 | 2365 |
| NRG4 | 755 |
| HRAS | 209 |
| NRG2 | -1156 |
| SHC1 | -1493 |
| SOS1 | -1772 |
| HBEGF | -1977 |
| GeneID | Gene Rank |
|---|---|
| ERBB4 | 6841 |
| NRAS | 5491 |
| NRG1 | 5376 |
| NRG3 | 5354 |
| KRAS | 4959 |
| EREG | 3888 |
| BTC | 3507 |
| GRB2 | 2365 |
| NRG4 | 755 |
| HRAS | 209 |
| NRG2 | -1156 |
| SHC1 | -1493 |
| SOS1 | -1772 |
| HBEGF | -1977 |
Regulation of IFNA signaling
| 973 | |
|---|---|
| set | Regulation of IFNA signaling |
| setSize | 25 |
| pANOVA | 0.000486 |
| s.dist | 0.403 |
| p.adjustANOVA | 0.052 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IFNA1 | 7051 |
| IFNA10 | 7051 |
| IFNA14 | 7051 |
| IFNA16 | 7051 |
| IFNA17 | 7051 |
| IFNA2 | 7051 |
| IFNA21 | 7051 |
| IFNA4 | 7051 |
| IFNA5 | 7051 |
| IFNA6 | 7051 |
| IFNA7 | 7051 |
| IFNA8 | 7051 |
| IFNB1 | 5508 |
| SOCS1 | 2387 |
| JAK1 | 1554 |
| IFNAR1 | 847 |
| STAT2 | -781 |
| STAT1 | -1859 |
| PTPN1 | -2109 |
| PTPN11 | -2492 |
| GeneID | Gene Rank |
|---|---|
| IFNA1 | 7051.0 |
| IFNA10 | 7051.0 |
| IFNA14 | 7051.0 |
| IFNA16 | 7051.0 |
| IFNA17 | 7051.0 |
| IFNA2 | 7051.0 |
| IFNA21 | 7051.0 |
| IFNA4 | 7051.0 |
| IFNA5 | 7051.0 |
| IFNA6 | 7051.0 |
| IFNA7 | 7051.0 |
| IFNA8 | 7051.0 |
| IFNB1 | 5508.0 |
| SOCS1 | 2387.0 |
| JAK1 | 1554.0 |
| IFNAR1 | 847.0 |
| STAT2 | -781.0 |
| STAT1 | -1859.0 |
| PTPN1 | -2109.0 |
| PTPN11 | -2492.0 |
| USP18 | -4333.5 |
| IFNAR2 | -5214.0 |
| TYK2 | -6660.0 |
| SOCS3 | -6938.0 |
| PTPN6 | -8620.0 |
Diseases associated with glycosylation precursor biosynthesis
| 292 | |
|---|---|
| set | Diseases associated with glycosylation precursor biosynthesis |
| setSize | 16 |
| pANOVA | 0.00547 |
| s.dist | -0.401 |
| p.adjustANOVA | 0.331 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CTSA | -9110.0 |
| GALE | -8957.0 |
| DHDDS | -8835.0 |
| NEU1 | -8439.0 |
| SRD5A3 | -8419.0 |
| GNE | -7079.0 |
| GALK1 | -6886.0 |
| DPM1 | -6145.0 |
| MPI | -5468.0 |
| PGM1 | -3767.0 |
| GALT | -2461.5 |
| PMM2 | -895.0 |
| GFPT1 | -342.0 |
| DPM3 | 1347.0 |
| DPM2 | 2129.0 |
| NUS1 | 4064.0 |
| GeneID | Gene Rank |
|---|---|
| CTSA | -9110.0 |
| GALE | -8957.0 |
| DHDDS | -8835.0 |
| NEU1 | -8439.0 |
| SRD5A3 | -8419.0 |
| GNE | -7079.0 |
| GALK1 | -6886.0 |
| DPM1 | -6145.0 |
| MPI | -5468.0 |
| PGM1 | -3767.0 |
| GALT | -2461.5 |
| PMM2 | -895.0 |
| GFPT1 | -342.0 |
| DPM3 | 1347.0 |
| DPM2 | 2129.0 |
| NUS1 | 4064.0 |
ATF6 (ATF6-alpha) activates chaperones
| 19 | |
|---|---|
| set | ATF6 (ATF6-alpha) activates chaperones |
| setSize | 10 |
| pANOVA | 0.0294 |
| s.dist | 0.398 |
| p.adjustANOVA | 0.439 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HSPA5 | 5620 |
| NFYC | 5412 |
| MBTPS2 | 4249 |
| ATF4 | 4245 |
| ATF6 | 4203 |
| HSP90B1 | 4163 |
| NFYA | 1594 |
| MBTPS1 | -442 |
| XBP1 | -2549 |
| NFYB | -4531 |
| GeneID | Gene Rank |
|---|---|
| HSPA5 | 5620 |
| NFYC | 5412 |
| MBTPS2 | 4249 |
| ATF4 | 4245 |
| ATF6 | 4203 |
| HSP90B1 | 4163 |
| NFYA | 1594 |
| MBTPS1 | -442 |
| XBP1 | -2549 |
| NFYB | -4531 |
Glutathione synthesis and recycling
| 474 | |
|---|---|
| set | Glutathione synthesis and recycling |
| setSize | 12 |
| pANOVA | 0.018 |
| s.dist | -0.394 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| OPLAH | -9057 |
| GGT1 | -8800 |
| GGT6 | -8757 |
| GGT7 | -7224 |
| GGT5 | -7220 |
| CHAC1 | -7129 |
| CNDP2 | -4417 |
| GGCT | -3618 |
| GSS | -709 |
| GCLC | -358 |
| GCLM | 1033 |
| CHAC2 | 4951 |
| GeneID | Gene Rank |
|---|---|
| OPLAH | -9057 |
| GGT1 | -8800 |
| GGT6 | -8757 |
| GGT7 | -7224 |
| GGT5 | -7220 |
| CHAC1 | -7129 |
| CNDP2 | -4417 |
| GGCT | -3618 |
| GSS | -709 |
| GCLC | -358 |
| GCLM | 1033 |
| CHAC2 | 4951 |
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation
| 525 | |
|---|---|
| set | IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation |
| setSize | 12 |
| pANOVA | 0.0195 |
| s.dist | 0.39 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TAB2 | 6463.0 |
| TLR4 | 5985.0 |
| MAP3K7 | 5044.0 |
| LY96 | 4026.0 |
| TAB3 | 4017.0 |
| TRAF6 | 3268.0 |
| TICAM2 | 3184.5 |
| UBA52 | 1870.0 |
| TICAM1 | 675.0 |
| CD14 | 227.0 |
| TAB1 | -2561.0 |
| IRAK2 | -6655.0 |
| GeneID | Gene Rank |
|---|---|
| TAB2 | 6463.0 |
| TLR4 | 5985.0 |
| MAP3K7 | 5044.0 |
| LY96 | 4026.0 |
| TAB3 | 4017.0 |
| TRAF6 | 3268.0 |
| TICAM2 | 3184.5 |
| UBA52 | 1870.0 |
| TICAM1 | 675.0 |
| CD14 | 227.0 |
| TAB1 | -2561.0 |
| IRAK2 | -6655.0 |
GRB2 events in ERBB2 signaling
| 445 | |
|---|---|
| set | GRB2 events in ERBB2 signaling |
| setSize | 16 |
| pANOVA | 0.00719 |
| s.dist | 0.388 |
| p.adjustANOVA | 0.374 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ERBB4 | 6841 |
| NRAS | 5491 |
| EGFR | 5410 |
| NRG1 | 5376 |
| NRG3 | 5354 |
| KRAS | 4959 |
| EREG | 3888 |
| BTC | 3507 |
| GRB2 | 2365 |
| EGF | 1889 |
| NRG4 | 755 |
| HRAS | 209 |
| NRG2 | -1156 |
| SOS1 | -1772 |
| HBEGF | -1977 |
| ERBB2 | -7283 |
| GeneID | Gene Rank |
|---|---|
| ERBB4 | 6841 |
| NRAS | 5491 |
| EGFR | 5410 |
| NRG1 | 5376 |
| NRG3 | 5354 |
| KRAS | 4959 |
| EREG | 3888 |
| BTC | 3507 |
| GRB2 | 2365 |
| EGF | 1889 |
| NRG4 | 755 |
| HRAS | 209 |
| NRG2 | -1156 |
| SOS1 | -1772 |
| HBEGF | -1977 |
| ERBB2 | -7283 |
CREB1 phosphorylation through the activation of Adenylate Cyclase
| 139 | |
|---|---|
| set | CREB1 phosphorylation through the activation of Adenylate Cyclase |
| setSize | 11 |
| pANOVA | 0.0269 |
| s.dist | 0.385 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PRKX | 5235 |
| CREB1 | 4499 |
| ADCY8 | 4229 |
| ADCY1 | 4198 |
| PRKAR2B | 3621 |
| CALM1 | 2961 |
| PRKACB | 2922 |
| PRKAR2A | 1973 |
| PRKACA | 303 |
| PRKAR1A | -1287 |
| PRKAR1B | -5621 |
| GeneID | Gene Rank |
|---|---|
| PRKX | 5235 |
| CREB1 | 4499 |
| ADCY8 | 4229 |
| ADCY1 | 4198 |
| PRKAR2B | 3621 |
| CALM1 | 2961 |
| PRKACB | 2922 |
| PRKAR2A | 1973 |
| PRKACA | 303 |
| PRKAR1A | -1287 |
| PRKAR1B | -5621 |
Synthesis of PA
| 1192 | |
|---|---|
| set | Synthesis of PA |
| setSize | 30 |
| pANOVA | 0.000268 |
| s.dist | -0.384 |
| p.adjustANOVA | 0.0339 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ALPI | -9214 |
| PLD2 | -8938 |
| AGPAT1 | -8913 |
| PLA2G1B | -8445 |
| GNPAT | -8171 |
| GPD1 | -7921 |
| PLA2G5 | -7617 |
| LPCAT4 | -7301 |
| PLA2G2D | -7131 |
| GPD1L | -7062 |
| PLA2G2F | -6730 |
| GPAT2 | -6614 |
| AGPAT4 | -5666 |
| PLA2G2E | -5483 |
| PLD6 | -5121 |
| PLA2R1 | -4923 |
| ACP6 | -4904 |
| PLA2G12A | -4250 |
| LIPH | -3356 |
| LPCAT1 | -2488 |
| GeneID | Gene Rank |
|---|---|
| ALPI | -9214 |
| PLD2 | -8938 |
| AGPAT1 | -8913 |
| PLA2G1B | -8445 |
| GNPAT | -8171 |
| GPD1 | -7921 |
| PLA2G5 | -7617 |
| LPCAT4 | -7301 |
| PLA2G2D | -7131 |
| GPD1L | -7062 |
| PLA2G2F | -6730 |
| GPAT2 | -6614 |
| AGPAT4 | -5666 |
| PLA2G2E | -5483 |
| PLD6 | -5121 |
| PLA2R1 | -4923 |
| ACP6 | -4904 |
| PLA2G12A | -4250 |
| LIPH | -3356 |
| LPCAT1 | -2488 |
| AGPAT2 | -2231 |
| PLA2G4D | -2011 |
| DDHD1 | -1900 |
| PLD1 | -1714 |
| AGPAT3 | -1623 |
| GPD2 | 277 |
| AGPAT5 | 1928 |
| LCLAT1 | 2146 |
| PLA2G4A | 3973 |
| GPAM | 5692 |
Mitotic Telophase/Cytokinesis
| 692 | |
|---|---|
| set | Mitotic Telophase/Cytokinesis |
| setSize | 10 |
| pANOVA | 0.0358 |
| s.dist | 0.383 |
| p.adjustANOVA | 0.469 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| STAG1 | 5580 |
| RAD21 | 5519 |
| NIPBL | 4783 |
| KIF23 | 3861 |
| PDS5B | 3739 |
| STAG2 | 3040 |
| SMC1A | 2320 |
| KIF20A | 153 |
| PDS5A | -2346 |
| SMC3 | -5863 |
| GeneID | Gene Rank |
|---|---|
| STAG1 | 5580 |
| RAD21 | 5519 |
| NIPBL | 4783 |
| KIF23 | 3861 |
| PDS5B | 3739 |
| STAG2 | 3040 |
| SMC1A | 2320 |
| KIF20A | 153 |
| PDS5A | -2346 |
| SMC3 | -5863 |
Adherens junctions interactions
| 65 | |
|---|---|
| set | Adherens junctions interactions |
| setSize | 24 |
| pANOVA | 0.0012 |
| s.dist | 0.382 |
| p.adjustANOVA | 0.111 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CDH7 | 6822 |
| CDH10 | 6750 |
| CDH9 | 6657 |
| CADM2 | 6651 |
| CDH11 | 6441 |
| CDH18 | 6299 |
| CDH2 | 6055 |
| CDH8 | 5417 |
| ANG | 5192 |
| CDH12 | 5113 |
| CDH17 | 4109 |
| CTNND1 | 3831 |
| CTNNA1 | 3807 |
| CDH6 | 3664 |
| CADM1 | 3296 |
| CADM3 | 1799 |
| CTNNB1 | 1225 |
| CDH3 | 12 |
| CDH1 | -1398 |
| CDH5 | -4900 |
| GeneID | Gene Rank |
|---|---|
| CDH7 | 6822 |
| CDH10 | 6750 |
| CDH9 | 6657 |
| CADM2 | 6651 |
| CDH11 | 6441 |
| CDH18 | 6299 |
| CDH2 | 6055 |
| CDH8 | 5417 |
| ANG | 5192 |
| CDH12 | 5113 |
| CDH17 | 4109 |
| CTNND1 | 3831 |
| CTNNA1 | 3807 |
| CDH6 | 3664 |
| CADM1 | 3296 |
| CADM3 | 1799 |
| CTNNB1 | 1225 |
| CDH3 | 12 |
| CDH1 | -1398 |
| CDH5 | -4900 |
| CDH15 | -5595 |
| CDH13 | -5750 |
| CDH4 | -7414 |
| JUP | -8552 |
GRB2 events in EGFR signaling
| 444 | |
|---|---|
| set | GRB2 events in EGFR signaling |
| setSize | 13 |
| pANOVA | 0.0172 |
| s.dist | 0.382 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491.0 |
| EGFR | 5410.0 |
| KRAS | 4959.0 |
| EREG | 3888.0 |
| BTC | 3507.0 |
| GRB2 | 2365.0 |
| EGF | 1889.0 |
| EPGN | 1733.0 |
| TGFA | 1407.0 |
| HRAS | 209.0 |
| AREG | -267.5 |
| SOS1 | -1772.0 |
| HBEGF | -1977.0 |
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491.0 |
| EGFR | 5410.0 |
| KRAS | 4959.0 |
| EREG | 3888.0 |
| BTC | 3507.0 |
| GRB2 | 2365.0 |
| EGF | 1889.0 |
| EPGN | 1733.0 |
| TGFA | 1407.0 |
| HRAS | 209.0 |
| AREG | -267.5 |
| SOS1 | -1772.0 |
| HBEGF | -1977.0 |
MET activates RAP1 and RAC1
| 634 | |
|---|---|
| set | MET activates RAP1 and RAC1 |
| setSize | 11 |
| pANOVA | 0.0307 |
| s.dist | 0.376 |
| p.adjustANOVA | 0.45 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CRKL | 6541 |
| HGF | 6189 |
| GAB1 | 4240 |
| RAP1A | 3687 |
| MET | 3362 |
| GRB2 | 2365 |
| RAC1 | 2318 |
| CRK | 1832 |
| DOCK7 | 187 |
| RAP1B | 55 |
| RAPGEF1 | -8561 |
| GeneID | Gene Rank |
|---|---|
| CRKL | 6541 |
| HGF | 6189 |
| GAB1 | 4240 |
| RAP1A | 3687 |
| MET | 3362 |
| GRB2 | 2365 |
| RAC1 | 2318 |
| CRK | 1832 |
| DOCK7 | 187 |
| RAP1B | 55 |
| RAPGEF1 | -8561 |
Metabolism of folate and pterines
| 654 | |
|---|---|
| set | Metabolism of folate and pterines |
| setSize | 14 |
| pANOVA | 0.0154 |
| s.dist | -0.374 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MTHFR | -8871.0 |
| FPGS | -8494.0 |
| SHMT2 | -8425.0 |
| SLC46A1 | -8326.0 |
| ALDH1L2 | -7253.0 |
| MTHFD2 | -7190.0 |
| SLC19A1 | -7067.0 |
| SHMT1 | -5678.0 |
| FOLR2 | -3279.0 |
| ALDH1L1 | -1290.0 |
| DHFR | 456.5 |
| MTHFD1 | 639.0 |
| MTHFD2L | 2536.0 |
| MTHFS | 4748.5 |
| GeneID | Gene Rank |
|---|---|
| MTHFR | -8871.0 |
| FPGS | -8494.0 |
| SHMT2 | -8425.0 |
| SLC46A1 | -8326.0 |
| ALDH1L2 | -7253.0 |
| MTHFD2 | -7190.0 |
| SLC19A1 | -7067.0 |
| SHMT1 | -5678.0 |
| FOLR2 | -3279.0 |
| ALDH1L1 | -1290.0 |
| DHFR | 456.5 |
| MTHFD1 | 639.0 |
| MTHFD2L | 2536.0 |
| MTHFS | 4748.5 |
Dermatan sulfate biosynthesis
| 280 | |
|---|---|
| set | Dermatan sulfate biosynthesis |
| setSize | 11 |
| pANOVA | 0.0319 |
| s.dist | 0.374 |
| p.adjustANOVA | 0.451 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DSEL | 6844 |
| DCN | 5899 |
| VCAN | 5365 |
| BCAN | 4670 |
| DSE | 4578 |
| BGN | 2641 |
| UST | 1493 |
| NCAN | -23 |
| CSPG5 | -2239 |
| CHST14 | -2584 |
| CSPG4 | -4661 |
| GeneID | Gene Rank |
|---|---|
| DSEL | 6844 |
| DCN | 5899 |
| VCAN | 5365 |
| BCAN | 4670 |
| DSE | 4578 |
| BGN | 2641 |
| UST | 1493 |
| NCAN | -23 |
| CSPG5 | -2239 |
| CHST14 | -2584 |
| CSPG4 | -4661 |
Glutamate and glutamine metabolism
| 471 | |
|---|---|
| set | Glutamate and glutamine metabolism |
| setSize | 13 |
| pANOVA | 0.0216 |
| s.dist | -0.368 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GLS2 | -8715.0 |
| PYCR2 | -8453.5 |
| PYCR1 | -8202.0 |
| ALDH18A1 | -7982.0 |
| GLUL | -6015.0 |
| GLUD1 | -4348.5 |
| GLUD2 | -4348.5 |
| GOT2 | -4194.0 |
| PYCRL | -3186.0 |
| RIMKLA | -2819.0 |
| OAT | -2089.0 |
| RIMKLB | 1045.0 |
| GLS | 6534.0 |
| GeneID | Gene Rank |
|---|---|
| GLS2 | -8715.0 |
| PYCR2 | -8453.5 |
| PYCR1 | -8202.0 |
| ALDH18A1 | -7982.0 |
| GLUL | -6015.0 |
| GLUD1 | -4348.5 |
| GLUD2 | -4348.5 |
| GOT2 | -4194.0 |
| PYCRL | -3186.0 |
| RIMKLA | -2819.0 |
| OAT | -2089.0 |
| RIMKLB | 1045.0 |
| GLS | 6534.0 |
Acyl chain remodelling of PS
| 61 | |
|---|---|
| set | Acyl chain remodelling of PS |
| setSize | 18 |
| pANOVA | 0.00855 |
| s.dist | -0.358 |
| p.adjustANOVA | 0.374 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| OSBPL10 | -9089 |
| PLA2G1B | -8445 |
| LPCAT3 | -7783 |
| PLA2G5 | -7617 |
| LPCAT4 | -7301 |
| PLA2G2D | -7131 |
| PLA2G2F | -6730 |
| OSBPL5 | -5977 |
| PLA2G2E | -5483 |
| PLA2R1 | -4923 |
| PLA2G12A | -4250 |
| PLA1A | -4239 |
| PLA2G4D | -2011 |
| PLA2G4F | -434 |
| PLA2G4E | 807 |
| MBOAT1 | 1142 |
| OSBPL8 | 3909 |
| PLA2G4A | 3973 |
| GeneID | Gene Rank |
|---|---|
| OSBPL10 | -9089 |
| PLA2G1B | -8445 |
| LPCAT3 | -7783 |
| PLA2G5 | -7617 |
| LPCAT4 | -7301 |
| PLA2G2D | -7131 |
| PLA2G2F | -6730 |
| OSBPL5 | -5977 |
| PLA2G2E | -5483 |
| PLA2R1 | -4923 |
| PLA2G12A | -4250 |
| PLA1A | -4239 |
| PLA2G4D | -2011 |
| PLA2G4F | -434 |
| PLA2G4E | 807 |
| MBOAT1 | 1142 |
| OSBPL8 | 3909 |
| PLA2G4A | 3973 |
Pre-NOTCH Processing in Golgi
| 868 | |
|---|---|
| set | Pre-NOTCH Processing in Golgi |
| setSize | 14 |
| pANOVA | 0.0208 |
| s.dist | -0.357 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NOTCH4 | -9076 |
| MFNG | -8096 |
| FURIN | -8045 |
| ST3GAL3 | -7923 |
| NOTCH1 | -7799 |
| ATP2A1 | -7579 |
| ATP2A3 | -4137 |
| SEL1L | -3864 |
| TMED2 | -2242 |
| B4GALT1 | -1731 |
| NOTCH3 | -1542 |
| LFNG | -220 |
| ATP2A2 | 3174 |
| ST3GAL6 | 3537 |
| GeneID | Gene Rank |
|---|---|
| NOTCH4 | -9076 |
| MFNG | -8096 |
| FURIN | -8045 |
| ST3GAL3 | -7923 |
| NOTCH1 | -7799 |
| ATP2A1 | -7579 |
| ATP2A3 | -4137 |
| SEL1L | -3864 |
| TMED2 | -2242 |
| B4GALT1 | -1731 |
| NOTCH3 | -1542 |
| LFNG | -220 |
| ATP2A2 | 3174 |
| ST3GAL6 | 3537 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression
| 334 | |
|---|---|
| set | ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression |
| setSize | 14 |
| pANOVA | 0.0218 |
| s.dist | -0.354 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| EHMT2 | -9212 |
| CHD3 | -8990 |
| MTA1 | -8619 |
| MTA3 | -8170 |
| MTA2 | -7441 |
| MBD3 | -7021 |
| CHD4 | -6350 |
| H2AFX | -5715 |
| TTF1 | -1611 |
| RBBP7 | -1280 |
| GATAD2A | -766 |
| HDAC2 | 2329 |
| GATAD2B | 3574 |
| ERCC6 | 4030 |
| GeneID | Gene Rank |
|---|---|
| EHMT2 | -9212 |
| CHD3 | -8990 |
| MTA1 | -8619 |
| MTA3 | -8170 |
| MTA2 | -7441 |
| MBD3 | -7021 |
| CHD4 | -6350 |
| H2AFX | -5715 |
| TTF1 | -1611 |
| RBBP7 | -1280 |
| GATAD2A | -766 |
| HDAC2 | 2329 |
| GATAD2B | 3574 |
| ERCC6 | 4030 |
Aflatoxin activation and detoxification
| 67 | |
|---|---|
| set | Aflatoxin activation and detoxification |
| setSize | 16 |
| pANOVA | 0.0144 |
| s.dist | -0.353 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DPEP3 | -8857.0 |
| GGT1 | -8800.0 |
| GGT6 | -8757.0 |
| ACY3 | -7418.0 |
| GGT7 | -7224.0 |
| GGT5 | -7220.0 |
| CYP2A13 | -7181.0 |
| CYP1A2 | -6503.0 |
| DPEP1 | -6306.0 |
| ACY1 | -6052.5 |
| MGST2 | -3758.0 |
| DPEP2 | -3462.0 |
| MGST1 | 654.0 |
| MGST3 | 3678.0 |
| CYP3A4 | 7085.5 |
| CYP3A5 | 7085.5 |
| GeneID | Gene Rank |
|---|---|
| DPEP3 | -8857.0 |
| GGT1 | -8800.0 |
| GGT6 | -8757.0 |
| ACY3 | -7418.0 |
| GGT7 | -7224.0 |
| GGT5 | -7220.0 |
| CYP2A13 | -7181.0 |
| CYP1A2 | -6503.0 |
| DPEP1 | -6306.0 |
| ACY1 | -6052.5 |
| MGST2 | -3758.0 |
| DPEP2 | -3462.0 |
| MGST1 | 654.0 |
| MGST3 | 3678.0 |
| CYP3A4 | 7085.5 |
| CYP3A5 | 7085.5 |
SHC1 events in EGFR signaling
| 1056 | |
|---|---|
| set | SHC1 events in EGFR signaling |
| setSize | 14 |
| pANOVA | 0.0231 |
| s.dist | 0.351 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491.0 |
| EGFR | 5410.0 |
| KRAS | 4959.0 |
| EREG | 3888.0 |
| BTC | 3507.0 |
| GRB2 | 2365.0 |
| EGF | 1889.0 |
| EPGN | 1733.0 |
| TGFA | 1407.0 |
| HRAS | 209.0 |
| AREG | -267.5 |
| SHC1 | -1493.0 |
| SOS1 | -1772.0 |
| HBEGF | -1977.0 |
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491.0 |
| EGFR | 5410.0 |
| KRAS | 4959.0 |
| EREG | 3888.0 |
| BTC | 3507.0 |
| GRB2 | 2365.0 |
| EGF | 1889.0 |
| EPGN | 1733.0 |
| TGFA | 1407.0 |
| HRAS | 209.0 |
| AREG | -267.5 |
| SHC1 | -1493.0 |
| SOS1 | -1772.0 |
| HBEGF | -1977.0 |
Termination of O-glycan biosynthesis
| 1251 | |
|---|---|
| set | Termination of O-glycan biosynthesis |
| setSize | 19 |
| pANOVA | 0.00985 |
| s.dist | -0.342 |
| p.adjustANOVA | 0.415 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MUC17 | -8569 |
| MUC2 | -8374 |
| ST3GAL3 | -7923 |
| ST6GALNAC2 | -7897 |
| MUC1 | -7388 |
| ST6GAL1 | -6796 |
| MUC6 | -6495 |
| MUC3A | -6178 |
| MUC4 | -5586 |
| ST3GAL1 | -4911 |
| ST3GAL2 | -4322 |
| MUC20 | -3067 |
| MUC19 | -2534 |
| ST6GALNAC4 | -1430 |
| MUC5B | -1392 |
| ST6GALNAC3 | -1364 |
| MUC13 | -322 |
| MUC15 | 4876 |
| MUC16 | 6597 |
| GeneID | Gene Rank |
|---|---|
| MUC17 | -8569 |
| MUC2 | -8374 |
| ST3GAL3 | -7923 |
| ST6GALNAC2 | -7897 |
| MUC1 | -7388 |
| ST6GAL1 | -6796 |
| MUC6 | -6495 |
| MUC3A | -6178 |
| MUC4 | -5586 |
| ST3GAL1 | -4911 |
| ST3GAL2 | -4322 |
| MUC20 | -3067 |
| MUC19 | -2534 |
| ST6GALNAC4 | -1430 |
| MUC5B | -1392 |
| ST6GALNAC3 | -1364 |
| MUC13 | -322 |
| MUC15 | 4876 |
| MUC16 | 6597 |
PI3K events in ERBB2 signaling
| 801 | |
|---|---|
| set | PI3K events in ERBB2 signaling |
| setSize | 16 |
| pANOVA | 0.0199 |
| s.dist | 0.336 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ERBB4 | 6841 |
| EGFR | 5410 |
| NRG1 | 5376 |
| NRG3 | 5354 |
| GAB1 | 4240 |
| EREG | 3888 |
| PIK3R1 | 3668 |
| BTC | 3507 |
| GRB2 | 2365 |
| EGF | 1889 |
| NRG4 | 755 |
| NRG2 | -1156 |
| HBEGF | -1977 |
| PIK3CA | -2203 |
| ERBB3 | -3610 |
| ERBB2 | -7283 |
| GeneID | Gene Rank |
|---|---|
| ERBB4 | 6841 |
| EGFR | 5410 |
| NRG1 | 5376 |
| NRG3 | 5354 |
| GAB1 | 4240 |
| EREG | 3888 |
| PIK3R1 | 3668 |
| BTC | 3507 |
| GRB2 | 2365 |
| EGF | 1889 |
| NRG4 | 755 |
| NRG2 | -1156 |
| HBEGF | -1977 |
| PIK3CA | -2203 |
| ERBB3 | -3610 |
| ERBB2 | -7283 |
Activation of RAC1
| 48 | |
|---|---|
| set | Activation of RAC1 |
| setSize | 12 |
| pANOVA | 0.0443 |
| s.dist | 0.335 |
| p.adjustANOVA | 0.501 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SLIT2 | 6943 |
| PAK3 | 6663 |
| NCK1 | 6344 |
| NCK2 | 4317 |
| ROBO1 | 4250 |
| PAK1 | 3151 |
| RAC1 | 2318 |
| PAK6 | 1017 |
| SOS2 | -1075 |
| SOS1 | -1772 |
| PAK2 | -5918 |
| PAK4 | -6018 |
| GeneID | Gene Rank |
|---|---|
| SLIT2 | 6943 |
| PAK3 | 6663 |
| NCK1 | 6344 |
| NCK2 | 4317 |
| ROBO1 | 4250 |
| PAK1 | 3151 |
| RAC1 | 2318 |
| PAK6 | 1017 |
| SOS2 | -1075 |
| SOS1 | -1772 |
| PAK2 | -5918 |
| PAK4 | -6018 |
Removal of the Flap Intermediate from the C-strand
| 1018 | |
|---|---|
| set | Removal of the Flap Intermediate from the C-strand |
| setSize | 12 |
| pANOVA | 0.0448 |
| s.dist | -0.335 |
| p.adjustANOVA | 0.501 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLD1 | -9075 |
| DNA2 | -8862 |
| POLD2 | -8726 |
| RPA2 | -8622 |
| TERF2 | -8116 |
| TINF2 | -5492 |
| PCNA | -5055 |
| RPA1 | -1771 |
| POLD3 | 1469 |
| POT1 | 2166 |
| TERF1 | 2795 |
| WRN | 3858 |
| GeneID | Gene Rank |
|---|---|
| POLD1 | -9075 |
| DNA2 | -8862 |
| POLD2 | -8726 |
| RPA2 | -8622 |
| TERF2 | -8116 |
| TINF2 | -5492 |
| PCNA | -5055 |
| RPA1 | -1771 |
| POLD3 | 1469 |
| POT1 | 2166 |
| TERF1 | 2795 |
| WRN | 3858 |
Gluconeogenesis
| 467 | |
|---|---|
| set | Gluconeogenesis |
| setSize | 29 |
| pANOVA | 0.00187 |
| s.dist | -0.334 |
| p.adjustANOVA | 0.163 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GPI | -9169 |
| SLC25A10 | -8904 |
| ENO2 | -8859 |
| GOT1 | -8224 |
| ALDOA | -8201 |
| PCK1 | -7630 |
| ALDOC | -7395 |
| ENO1 | -6673 |
| G6PC | -6411 |
| PGAM2 | -5773 |
| SLC25A1 | -5700 |
| FBP2 | -4989 |
| ENO3 | -4810 |
| FBP1 | -4764 |
| SLC25A11 | -4483 |
| GOT2 | -4194 |
| SLC37A2 | -3786 |
| GAPDHS | -3331 |
| SLC25A12 | -3201 |
| G6PC2 | -3111 |
| GeneID | Gene Rank |
|---|---|
| GPI | -9169 |
| SLC25A10 | -8904 |
| ENO2 | -8859 |
| GOT1 | -8224 |
| ALDOA | -8201 |
| PCK1 | -7630 |
| ALDOC | -7395 |
| ENO1 | -6673 |
| G6PC | -6411 |
| PGAM2 | -5773 |
| SLC25A1 | -5700 |
| FBP2 | -4989 |
| ENO3 | -4810 |
| FBP1 | -4764 |
| SLC25A11 | -4483 |
| GOT2 | -4194 |
| SLC37A2 | -3786 |
| GAPDHS | -3331 |
| SLC25A12 | -3201 |
| G6PC2 | -3111 |
| PCK2 | -2821 |
| SLC37A1 | -1624 |
| G6PC3 | -1510 |
| MDH1 | -739 |
| PGK2 | 668 |
| SLC25A13 | 1567 |
| PC | 3059 |
| ALDOB | 5326 |
| PGK1 | 6185 |
Processive synthesis on the lagging strand
| 882 | |
|---|---|
| set | Processive synthesis on the lagging strand |
| setSize | 12 |
| pANOVA | 0.0469 |
| s.dist | -0.331 |
| p.adjustANOVA | 0.501 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLD1 | -9075 |
| DNA2 | -8862 |
| POLD2 | -8726 |
| RPA2 | -8622 |
| PRIM1 | -7779 |
| POLA2 | -5833 |
| PCNA | -5055 |
| RPA1 | -1771 |
| PRIM2 | -50 |
| POLD3 | 1469 |
| LIG1 | 4144 |
| POLA1 | 5038 |
| GeneID | Gene Rank |
|---|---|
| POLD1 | -9075 |
| DNA2 | -8862 |
| POLD2 | -8726 |
| RPA2 | -8622 |
| PRIM1 | -7779 |
| POLA2 | -5833 |
| PCNA | -5055 |
| RPA1 | -1771 |
| PRIM2 | -50 |
| POLD3 | 1469 |
| LIG1 | 4144 |
| POLA1 | 5038 |
XBP1(S) activates chaperone genes
| 1355 | |
|---|---|
| set | XBP1(S) activates chaperone genes |
| setSize | 42 |
| pANOVA | 0.000305 |
| s.dist | -0.322 |
| p.adjustANOVA | 0.0354 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CUL7 | -9176 |
| ZBTB17 | -9080 |
| DCTN1 | -9067 |
| LMNA | -9031 |
| CXXC1 | -8842 |
| EXTL1 | -8708 |
| TLN1 | -8595 |
| HYOU1 | -8438 |
| TPP1 | -7932 |
| PPP2R5B | -7445 |
| SRPRB | -7255 |
| YIF1A | -6894 |
| WFS1 | -6026 |
| KDELR3 | -5611 |
| ARFGAP1 | -5054 |
| DNAJB11 | -4718 |
| SEC31A | -4705 |
| KLHDC3 | -4472 |
| EXTL3 | -4351 |
| ADD1 | -3969 |
| GeneID | Gene Rank |
|---|---|
| CUL7 | -9176.0 |
| ZBTB17 | -9080.0 |
| DCTN1 | -9067.0 |
| LMNA | -9031.0 |
| CXXC1 | -8842.0 |
| EXTL1 | -8708.0 |
| TLN1 | -8595.0 |
| HYOU1 | -8438.0 |
| TPP1 | -7932.0 |
| PPP2R5B | -7445.0 |
| SRPRB | -7255.0 |
| YIF1A | -6894.0 |
| WFS1 | -6026.0 |
| KDELR3 | -5611.0 |
| ARFGAP1 | -5054.0 |
| DNAJB11 | -4718.0 |
| SEC31A | -4705.0 |
| KLHDC3 | -4472.0 |
| EXTL3 | -4351.0 |
| ADD1 | -3969.0 |
| PDIA6 | -3493.0 |
| CTDSP2 | -3420.0 |
| SYVN1 | -3296.0 |
| ATP6V0D1 | -2912.0 |
| DDX11 | -2892.0 |
| FKBP14 | -2809.0 |
| XBP1 | -2549.0 |
| GSK3A | -1702.5 |
| SULT1A3 | -1527.5 |
| PDIA5 | -1504.0 |
| SHC1 | -1493.0 |
| EXTL2 | -1255.0 |
| HDGF | -713.0 |
| GFPT1 | -342.0 |
| SRPR | -302.0 |
| DNAJC3 | -203.0 |
| PREB | -53.0 |
| C19orf10 | 1373.0 |
| TSPYL2 | 1418.0 |
| WIPI1 | 1605.0 |
| SSR1 | 4780.0 |
| EDEM1 | 6137.0 |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1
| 595 | |
|---|---|
| set | JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 |
| setSize | 16 |
| pANOVA | 0.0264 |
| s.dist | 0.321 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MAPK8 | 6717 |
| TAB2 | 6463 |
| MAPK10 | 5903 |
| MAP3K7 | 5044 |
| MAP2K4 | 4935 |
| TAB3 | 4017 |
| TRAF6 | 3268 |
| IRAK1 | 2480 |
| NOD1 | 2465 |
| IKBKG | 1899 |
| MAPK9 | 1597 |
| UBE2N | -257 |
| TAB1 | -2561 |
| NOD2 | -2707 |
| IRAK2 | -6655 |
| MAP2K7 | -7581 |
| GeneID | Gene Rank |
|---|---|
| MAPK8 | 6717 |
| TAB2 | 6463 |
| MAPK10 | 5903 |
| MAP3K7 | 5044 |
| MAP2K4 | 4935 |
| TAB3 | 4017 |
| TRAF6 | 3268 |
| IRAK1 | 2480 |
| NOD1 | 2465 |
| IKBKG | 1899 |
| MAPK9 | 1597 |
| UBE2N | -257 |
| TAB1 | -2561 |
| NOD2 | -2707 |
| IRAK2 | -6655 |
| MAP2K7 | -7581 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants
| 212 | |
|---|---|
| set | Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants |
| setSize | 16 |
| pANOVA | 0.0269 |
| s.dist | 0.319 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491 |
| EGFR | 5410 |
| KRAS | 4959 |
| GAB1 | 4240 |
| PIK3R1 | 3668 |
| CBL | 2832 |
| PLCG1 | 2753 |
| GRB2 | 2365 |
| EGF | 1889 |
| UBA52 | 1870 |
| CDC37 | 1195 |
| HRAS | 209 |
| SHC1 | -1493 |
| SOS1 | -1772 |
| PIK3CA | -2203 |
| HSP90AA1 | -6528 |
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491 |
| EGFR | 5410 |
| KRAS | 4959 |
| GAB1 | 4240 |
| PIK3R1 | 3668 |
| CBL | 2832 |
| PLCG1 | 2753 |
| GRB2 | 2365 |
| EGF | 1889 |
| UBA52 | 1870 |
| CDC37 | 1195 |
| HRAS | 209 |
| SHC1 | -1493 |
| SOS1 | -1772 |
| PIK3CA | -2203 |
| HSP90AA1 | -6528 |
Signaling by Ligand-Responsive EGFR Variants in Cancer
| 1128 | |
|---|---|
| set | Signaling by Ligand-Responsive EGFR Variants in Cancer |
| setSize | 16 |
| pANOVA | 0.0269 |
| s.dist | 0.319 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491 |
| EGFR | 5410 |
| KRAS | 4959 |
| GAB1 | 4240 |
| PIK3R1 | 3668 |
| CBL | 2832 |
| PLCG1 | 2753 |
| GRB2 | 2365 |
| EGF | 1889 |
| UBA52 | 1870 |
| CDC37 | 1195 |
| HRAS | 209 |
| SHC1 | -1493 |
| SOS1 | -1772 |
| PIK3CA | -2203 |
| HSP90AA1 | -6528 |
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491 |
| EGFR | 5410 |
| KRAS | 4959 |
| GAB1 | 4240 |
| PIK3R1 | 3668 |
| CBL | 2832 |
| PLCG1 | 2753 |
| GRB2 | 2365 |
| EGF | 1889 |
| UBA52 | 1870 |
| CDC37 | 1195 |
| HRAS | 209 |
| SHC1 | -1493 |
| SOS1 | -1772 |
| PIK3CA | -2203 |
| HSP90AA1 | -6528 |
TRAF6-mediated induction of TAK1 complex within TLR4 complex
| 1241 | |
|---|---|
| set | TRAF6-mediated induction of TAK1 complex within TLR4 complex |
| setSize | 13 |
| pANOVA | 0.0467 |
| s.dist | 0.319 |
| p.adjustANOVA | 0.501 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TAB2 | 6463.0 |
| TLR4 | 5985.0 |
| MAP3K7 | 5044.0 |
| LY96 | 4026.0 |
| TAB3 | 4017.0 |
| TRAF6 | 3268.0 |
| TICAM2 | 3184.5 |
| UBA52 | 1870.0 |
| TICAM1 | 675.0 |
| CD14 | 227.0 |
| TAB1 | -2561.0 |
| SARM1 | -5406.0 |
| IRAK2 | -6655.0 |
| GeneID | Gene Rank |
|---|---|
| TAB2 | 6463.0 |
| TLR4 | 5985.0 |
| MAP3K7 | 5044.0 |
| LY96 | 4026.0 |
| TAB3 | 4017.0 |
| TRAF6 | 3268.0 |
| TICAM2 | 3184.5 |
| UBA52 | 1870.0 |
| TICAM1 | 675.0 |
| CD14 | 227.0 |
| TAB1 | -2561.0 |
| SARM1 | -5406.0 |
| IRAK2 | -6655.0 |
Receptor-type tyrosine-protein phosphatases
| 956 | |
|---|---|
| set | Receptor-type tyrosine-protein phosphatases |
| setSize | 19 |
| pANOVA | 0.0162 |
| s.dist | 0.319 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PTPRD | 6719 |
| IL1RAP | 6424 |
| IL1RAPL1 | 6410 |
| SLITRK5 | 6215 |
| SLITRK4 | 6169 |
| IL1RAPL2 | 5902 |
| SLITRK1 | 5835 |
| SLITRK6 | 5719 |
| SLITRK3 | 4792 |
| SLITRK2 | 3617 |
| NTRK3 | 2619 |
| PPFIA1 | 914 |
| PPFIBP2 | -793 |
| LRRC4B | -2330 |
| PPFIBP1 | -2499 |
| PTPRS | -2990 |
| PPFIA3 | -6467 |
| PTPRF | -8218 |
| PPFIA4 | -8636 |
| GeneID | Gene Rank |
|---|---|
| PTPRD | 6719 |
| IL1RAP | 6424 |
| IL1RAPL1 | 6410 |
| SLITRK5 | 6215 |
| SLITRK4 | 6169 |
| IL1RAPL2 | 5902 |
| SLITRK1 | 5835 |
| SLITRK6 | 5719 |
| SLITRK3 | 4792 |
| SLITRK2 | 3617 |
| NTRK3 | 2619 |
| PPFIA1 | 914 |
| PPFIBP2 | -793 |
| LRRC4B | -2330 |
| PPFIBP1 | -2499 |
| PTPRS | -2990 |
| PPFIA3 | -6467 |
| PTPRF | -8218 |
| PPFIA4 | -8636 |
Polymerase switching on the C-strand of the telomere
| 856 | |
|---|---|
| set | Polymerase switching on the C-strand of the telomere |
| setSize | 21 |
| pANOVA | 0.0117 |
| s.dist | -0.318 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CHTF18 | -9097 |
| POLD1 | -9075 |
| POLD2 | -8726 |
| TERF2 | -8116 |
| PRIM1 | -7779 |
| RFC5 | -7623 |
| CTC1 | -7350 |
| TEN1 | -6308 |
| POLA2 | -5833 |
| TINF2 | -5492 |
| PCNA | -5055 |
| RFC3 | -4339 |
| RFC2 | -2032 |
| DSCC1 | -1557 |
| RFC1 | -726 |
| PRIM2 | -50 |
| RFC4 | 1109 |
| POLD3 | 1469 |
| POT1 | 2166 |
| TERF1 | 2795 |
| GeneID | Gene Rank |
|---|---|
| CHTF18 | -9097 |
| POLD1 | -9075 |
| POLD2 | -8726 |
| TERF2 | -8116 |
| PRIM1 | -7779 |
| RFC5 | -7623 |
| CTC1 | -7350 |
| TEN1 | -6308 |
| POLA2 | -5833 |
| TINF2 | -5492 |
| PCNA | -5055 |
| RFC3 | -4339 |
| RFC2 | -2032 |
| DSCC1 | -1557 |
| RFC1 | -726 |
| PRIM2 | -50 |
| RFC4 | 1109 |
| POLD3 | 1469 |
| POT1 | 2166 |
| TERF1 | 2795 |
| POLA1 | 5038 |
Constitutive Signaling by EGFRvIII
| 211 | |
|---|---|
| set | Constitutive Signaling by EGFRvIII |
| setSize | 15 |
| pANOVA | 0.0336 |
| s.dist | 0.317 |
| p.adjustANOVA | 0.463 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491 |
| EGFR | 5410 |
| KRAS | 4959 |
| GAB1 | 4240 |
| PIK3R1 | 3668 |
| CBL | 2832 |
| PLCG1 | 2753 |
| GRB2 | 2365 |
| EGF | 1889 |
| CDC37 | 1195 |
| HRAS | 209 |
| SHC1 | -1493 |
| SOS1 | -1772 |
| PIK3CA | -2203 |
| HSP90AA1 | -6528 |
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491 |
| EGFR | 5410 |
| KRAS | 4959 |
| GAB1 | 4240 |
| PIK3R1 | 3668 |
| CBL | 2832 |
| PLCG1 | 2753 |
| GRB2 | 2365 |
| EGF | 1889 |
| CDC37 | 1195 |
| HRAS | 209 |
| SHC1 | -1493 |
| SOS1 | -1772 |
| PIK3CA | -2203 |
| HSP90AA1 | -6528 |
Signaling by EGFRvIII in Cancer
| 1100 | |
|---|---|
| set | Signaling by EGFRvIII in Cancer |
| setSize | 15 |
| pANOVA | 0.0336 |
| s.dist | 0.317 |
| p.adjustANOVA | 0.463 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491 |
| EGFR | 5410 |
| KRAS | 4959 |
| GAB1 | 4240 |
| PIK3R1 | 3668 |
| CBL | 2832 |
| PLCG1 | 2753 |
| GRB2 | 2365 |
| EGF | 1889 |
| CDC37 | 1195 |
| HRAS | 209 |
| SHC1 | -1493 |
| SOS1 | -1772 |
| PIK3CA | -2203 |
| HSP90AA1 | -6528 |
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491 |
| EGFR | 5410 |
| KRAS | 4959 |
| GAB1 | 4240 |
| PIK3R1 | 3668 |
| CBL | 2832 |
| PLCG1 | 2753 |
| GRB2 | 2365 |
| EGF | 1889 |
| CDC37 | 1195 |
| HRAS | 209 |
| SHC1 | -1493 |
| SOS1 | -1772 |
| PIK3CA | -2203 |
| HSP90AA1 | -6528 |
Signaling by EGFR in Cancer
| 1099 | |
|---|---|
| set | Signaling by EGFR in Cancer |
| setSize | 22 |
| pANOVA | 0.0108 |
| s.dist | 0.314 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491.0 |
| EGFR | 5410.0 |
| KRAS | 4959.0 |
| GAB1 | 4240.0 |
| EREG | 3888.0 |
| PIK3R1 | 3668.0 |
| BTC | 3507.0 |
| CBL | 2832.0 |
| PLCG1 | 2753.0 |
| GRB2 | 2365.0 |
| EGF | 1889.0 |
| UBA52 | 1870.0 |
| EPGN | 1733.0 |
| TGFA | 1407.0 |
| CDC37 | 1195.0 |
| HRAS | 209.0 |
| AREG | -267.5 |
| SHC1 | -1493.0 |
| SOS1 | -1772.0 |
| HBEGF | -1977.0 |
| GeneID | Gene Rank |
|---|---|
| NRAS | 5491.0 |
| EGFR | 5410.0 |
| KRAS | 4959.0 |
| GAB1 | 4240.0 |
| EREG | 3888.0 |
| PIK3R1 | 3668.0 |
| BTC | 3507.0 |
| CBL | 2832.0 |
| PLCG1 | 2753.0 |
| GRB2 | 2365.0 |
| EGF | 1889.0 |
| UBA52 | 1870.0 |
| EPGN | 1733.0 |
| TGFA | 1407.0 |
| CDC37 | 1195.0 |
| HRAS | 209.0 |
| AREG | -267.5 |
| SHC1 | -1493.0 |
| SOS1 | -1772.0 |
| HBEGF | -1977.0 |
| PIK3CA | -2203.0 |
| HSP90AA1 | -6528.0 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest
| 1234 | |
|---|---|
| set | TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest |
| setSize | 17 |
| pANOVA | 0.0253 |
| s.dist | -0.313 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PRMT1 | -8681.0 |
| TP53 | -8478.0 |
| BAX | -7421.0 |
| CARM1 | -6875.0 |
| AURKA | -6481.0 |
| TFDP1 | -5656.5 |
| PCNA | -5055.0 |
| SFN | -4853.0 |
| CDK1 | -4276.0 |
| CCNB1 | -3071.0 |
| RBL2 | -2794.0 |
| RBL1 | -1786.0 |
| ZNF385A | -1134.0 |
| E2F4 | 140.0 |
| GADD45A | 1016.0 |
| EP300 | 1892.0 |
| TFDP2 | 2089.0 |
| GeneID | Gene Rank |
|---|---|
| PRMT1 | -8681.0 |
| TP53 | -8478.0 |
| BAX | -7421.0 |
| CARM1 | -6875.0 |
| AURKA | -6481.0 |
| TFDP1 | -5656.5 |
| PCNA | -5055.0 |
| SFN | -4853.0 |
| CDK1 | -4276.0 |
| CCNB1 | -3071.0 |
| RBL2 | -2794.0 |
| RBL1 | -1786.0 |
| ZNF385A | -1134.0 |
| E2F4 | 140.0 |
| GADD45A | 1016.0 |
| EP300 | 1892.0 |
| TFDP2 | 2089.0 |
CD209 (DC-SIGN) signaling
| 126 | |
|---|---|
| set | CD209 (DC-SIGN) signaling |
| setSize | 19 |
| pANOVA | 0.0184 |
| s.dist | 0.312 |
| p.adjustANOVA | 0.421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CD209 | 6987.5 |
| PAK3 | 6663.0 |
| LYN | 6366.0 |
| NRAS | 5491.0 |
| KRAS | 4959.0 |
| RELB | 4547.0 |
| PAK1 | 3151.0 |
| PRKACB | 2922.0 |
| RAF1 | 2301.0 |
| EP300 | 1892.0 |
| CREBBP | 1152.0 |
| FYN | 958.0 |
| PRKACA | 303.0 |
| HRAS | 209.0 |
| RPS6KA5 | -1192.0 |
| NFKB1 | -3161.0 |
| RELA | -3856.0 |
| ICAM2 | -5342.0 |
| PAK2 | -5918.0 |
| GeneID | Gene Rank |
|---|---|
| CD209 | 6987.5 |
| PAK3 | 6663.0 |
| LYN | 6366.0 |
| NRAS | 5491.0 |
| KRAS | 4959.0 |
| RELB | 4547.0 |
| PAK1 | 3151.0 |
| PRKACB | 2922.0 |
| RAF1 | 2301.0 |
| EP300 | 1892.0 |
| CREBBP | 1152.0 |
| FYN | 958.0 |
| PRKACA | 303.0 |
| HRAS | 209.0 |
| RPS6KA5 | -1192.0 |
| NFKB1 | -3161.0 |
| RELA | -3856.0 |
| ICAM2 | -5342.0 |
| PAK2 | -5918.0 |
Acyl chain remodelling of PI
| 60 | |
|---|---|
| set | Acyl chain remodelling of PI |
| setSize | 14 |
| pANOVA | 0.0433 |
| s.dist | -0.312 |
| p.adjustANOVA | 0.501 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PLA2G1B | -8445 |
| MBOAT7 | -7777 |
| PLA2G5 | -7617 |
| PLA2G2D | -7131 |
| PLA2G2F | -6730 |
| PLA2G2E | -5483 |
| PLBD1 | -4974 |
| PLA2R1 | -4923 |
| PLA2G12A | -4250 |
| PLA2G4D | -2011 |
| PLA2G4F | -434 |
| PLA2G4E | 807 |
| PLA2G4A | 3973 |
| PLA2G4C | 4574 |
| GeneID | Gene Rank |
|---|---|
| PLA2G1B | -8445 |
| MBOAT7 | -7777 |
| PLA2G5 | -7617 |
| PLA2G2D | -7131 |
| PLA2G2F | -6730 |
| PLA2G2E | -5483 |
| PLBD1 | -4974 |
| PLA2R1 | -4923 |
| PLA2G12A | -4250 |
| PLA2G4D | -2011 |
| PLA2G4F | -434 |
| PLA2G4E | 807 |
| PLA2G4A | 3973 |
| PLA2G4C | 4574 |
Signaling by Leptin
| 1127 | |
|---|---|
| set | Signaling by Leptin |
| setSize | 10 |
| pANOVA | 0.0882 |
| s.dist | -0.311 |
| p.adjustANOVA | 0.623 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| STAT3 | -8890 |
| STAT5A | -7671 |
| SOCS3 | -6938 |
| SH2B1 | -5696 |
| IRS1 | -5128 |
| LEP | -5051 |
| PTPN11 | -2492 |
| STAT5B | -2146 |
| LEPR | 2395 |
| JAK2 | 5647 |
| GeneID | Gene Rank |
|---|---|
| STAT3 | -8890 |
| STAT5A | -7671 |
| SOCS3 | -6938 |
| SH2B1 | -5696 |
| IRS1 | -5128 |
| LEP | -5051 |
| PTPN11 | -2492 |
| STAT5B | -2146 |
| LEPR | 2395 |
| JAK2 | 5647 |
Activated NTRK2 signals through FRS2 and FRS3
| 32 | |
|---|---|
| set | Activated NTRK2 signals through FRS2 and FRS3 |
| setSize | 10 |
| pANOVA | 0.0891 |
| s.dist | 0.31 |
| p.adjustANOVA | 0.623 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| BDNF | 6682 |
| NRAS | 5491 |
| KRAS | 4959 |
| GRB2 | 2365 |
| FRS2 | 752 |
| HRAS | 209 |
| NTF4 | -149 |
| NTRK2 | -1218 |
| SOS1 | -1772 |
| PTPN11 | -2492 |
| GeneID | Gene Rank |
|---|---|
| BDNF | 6682 |
| NRAS | 5491 |
| KRAS | 4959 |
| GRB2 | 2365 |
| FRS2 | 752 |
| HRAS | 209 |
| NTF4 | -149 |
| NTRK2 | -1218 |
| SOS1 | -1772 |
| PTPN11 | -2492 |
Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.0.2 (2020-06-22)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 18.04.4 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.7.1
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.7.1
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## attached base packages:
## [1] stats4 parallel stats graphics grDevices utils datasets
## [8] methods base
##
## other attached packages:
## [1] pkgload_1.1.0 GGally_2.0.0
## [3] beeswarm_0.2.3 gtools_3.8.2
## [5] echarts4r_0.3.2 mitch_1.0.6
## [7] fgsea_1.14.0 gplots_3.0.3
## [9] DESeq2_1.28.1 SummarizedExperiment_1.18.1
## [11] DelayedArray_0.14.0 matrixStats_0.56.0
## [13] Biobase_2.48.0 GenomicRanges_1.40.0
## [15] GenomeInfoDb_1.24.2 IRanges_2.22.2
## [17] S4Vectors_0.26.1 BiocGenerics_0.34.0
## [19] reshape2_1.4.4 forcats_0.5.0
## [21] stringr_1.4.0 dplyr_1.0.0
## [23] purrr_0.3.4 readr_1.3.1
## [25] tidyr_1.1.0 tibble_3.0.1
## [27] ggplot2_3.3.2 tidyverse_1.3.0
## [29] locfit_1.5-9.4 statmod_1.4.34
## [31] plyr_1.8.6
##
## loaded via a namespace (and not attached):
## [1] colorspace_1.4-1 ellipsis_0.3.1 rprojroot_1.3-2
## [4] XVector_0.28.0 fs_1.4.2 rstudioapi_0.11
## [7] farver_2.0.3 bit64_0.9-7 AnnotationDbi_1.50.1
## [10] fansi_0.4.1 lubridate_1.7.9 xml2_1.3.2
## [13] splines_4.0.2 geneplotter_1.66.0 knitr_1.29
## [16] jsonlite_1.7.0 broom_0.5.6 annotate_1.66.0
## [19] dbplyr_1.4.4 shiny_1.5.0 compiler_4.0.2
## [22] httr_1.4.1 backports_1.1.8 assertthat_0.2.1
## [25] Matrix_1.2-18 fastmap_1.0.1 cli_2.0.2
## [28] later_1.1.0.1 prettyunits_1.1.1 htmltools_0.5.0
## [31] tools_4.0.2 gtable_0.3.0 glue_1.4.1
## [34] GenomeInfoDbData_1.2.3 fastmatch_1.1-0 Rcpp_1.0.4.6
## [37] cellranger_1.1.0 vctrs_0.3.1 gdata_2.18.0
## [40] nlme_3.1-148 xfun_0.15 testthat_2.3.2
## [43] rvest_0.3.5 mime_0.9 lifecycle_0.2.0
## [46] XML_3.99-0.3 zlibbioc_1.34.0 MASS_7.3-51.6
## [49] scales_1.1.1 hms_0.5.3 promises_1.1.1
## [52] RColorBrewer_1.1-2 yaml_2.2.1 memoise_1.1.0
## [55] gridExtra_2.3 reshape_0.8.8 stringi_1.4.6
## [58] RSQLite_2.2.0 highr_0.8 genefilter_1.70.0
## [61] desc_1.2.0 caTools_1.18.0 BiocParallel_1.22.0
## [64] rlang_0.4.6 pkgconfig_2.0.3 bitops_1.0-6
## [67] evaluate_0.14 lattice_0.20-41 labeling_0.3
## [70] htmlwidgets_1.5.1 bit_1.1-15.2 tidyselect_1.1.0
## [73] magrittr_1.5 R6_2.4.1 generics_0.0.2
## [76] DBI_1.1.0 pillar_1.4.4 haven_2.3.1
## [79] withr_2.2.0 survival_3.2-3 RCurl_1.98-1.2
## [82] modelr_0.1.8 crayon_1.3.4 KernSmooth_2.23-17
## [85] rmarkdown_2.3 progress_1.2.2 grid_4.0.2
## [88] readxl_1.3.1 data.table_1.12.8 blob_1.2.1
## [91] reprex_0.3.0 digest_0.6.25 pbmcapply_1.5.0
## [94] xtable_1.8-4 httpuv_1.5.4 munsell_0.5.0
END of report