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 0.4023900
## A1BG 0.8276224
## A1CF -0.1176536
## A2M -1.9577707
## A3GALT2 0.6904985
## A4GALT -0.6623122
Here are some metrics about the input data profile:
| Profile metrics | |
|---|---|
| num_genesets | 2400 |
| num_genes_in_profile | 13888 |
| duplicated_genes_present | 0 |
| num_profile_genes_in_sets | 7447 |
| num_profile_genes_not_in_sets | 6441 |
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 | 1067 |
| num_genesets_included | 1333 |
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 |
|---|---|---|---|---|
| TRAF6 mediated IRF7 activation | 28 | 1.26e-06 | 0.529 | 0.00168 |
| Condensation of Prophase Chromosomes | 10 | 6.77e-03 | 0.495 | 0.63700 |
| Regulation of IFNA signaling | 23 | 1.21e-04 | 0.463 | 0.08080 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 11 | 9.08e-03 | 0.454 | 0.63700 |
| alpha-linolenic acid (ALA) metabolism | 11 | 9.08e-03 | 0.454 | 0.63700 |
| Heme degradation | 15 | 2.32e-03 | 0.454 | 0.36200 |
| E2F mediated regulation of DNA replication | 18 | 1.09e-03 | 0.445 | 0.29200 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 12 | 1.29e-02 | 0.415 | 0.74800 |
| Regulation of signaling by NODAL | 10 | 4.41e-02 | -0.368 | 0.85100 |
| Regulation of PTEN mRNA translation | 11 | 3.48e-02 | 0.368 | 0.85100 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 12 | 3.16e-02 | 0.358 | 0.85100 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 11 | 4.17e-02 | 0.355 | 0.85100 |
| Tandem pore domain potassium channels | 11 | 4.26e-02 | 0.353 | 0.85100 |
| Scavenging of heme from plasma | 10 | 5.39e-02 | -0.352 | 0.85100 |
| Metabolism of porphyrins | 25 | 2.45e-03 | 0.350 | 0.36200 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 11 | 5.14e-02 | 0.339 | 0.85100 |
| FOXO-mediated transcription of cell death genes | 13 | 3.69e-02 | 0.334 | 0.85100 |
| Citric acid cycle (TCA cycle) | 15 | 2.72e-02 | 0.329 | 0.85100 |
| Cyclin A/B1/B2 associated events during G2/M transition | 13 | 4.04e-02 | 0.328 | 0.85100 |
| Nucleotide-like (purinergic) receptors | 11 | 6.13e-02 | -0.326 | 0.85100 |
| Phase 4 - resting membrane potential | 17 | 2.01e-02 | 0.326 | 0.80800 |
| Diseases associated with the TLR signaling cascade | 18 | 1.89e-02 | -0.320 | 0.80800 |
| Diseases of Immune System | 18 | 1.89e-02 | -0.320 | 0.80800 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 16 | 2.82e-02 | 0.317 | 0.85100 |
| Eicosanoid ligand-binding receptors | 10 | 8.44e-02 | -0.315 | 0.85100 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 13 | 5.13e-02 | 0.312 | 0.85100 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 13 | 5.13e-02 | 0.312 | 0.85100 |
| TP53 Regulates Transcription of Death Receptors and Ligands | 10 | 8.87e-02 | 0.311 | 0.85300 |
| HS-GAG biosynthesis | 22 | 1.24e-02 | -0.308 | 0.74800 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 11 | 8.21e-02 | -0.303 | 0.85100 |
| Defective EXT2 causes exostoses 2 | 11 | 8.21e-02 | -0.303 | 0.85100 |
| Regulation of TP53 Activity through Methylation | 11 | 8.23e-02 | -0.303 | 0.85100 |
| Diseases of DNA repair | 10 | 1.09e-01 | 0.293 | 0.88500 |
| The role of Nef in HIV-1 replication and disease pathogenesis | 23 | 1.55e-02 | 0.291 | 0.76800 |
| ER Quality Control Compartment (ERQC) | 12 | 8.14e-02 | -0.291 | 0.85100 |
| Synthesis of PC | 20 | 2.50e-02 | 0.290 | 0.85100 |
| Defective B4GALT7 causes EDS, progeroid type | 15 | 5.46e-02 | -0.287 | 0.85100 |
| Norepinephrine Neurotransmitter Release Cycle | 12 | 8.78e-02 | -0.285 | 0.85300 |
| Smooth Muscle Contraction | 29 | 8.28e-03 | 0.283 | 0.63700 |
| Heme biosynthesis | 12 | 9.16e-02 | 0.281 | 0.85300 |
| Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 10 | 1.24e-01 | -0.281 | 0.88500 |
| Interferon alpha/beta signaling | 50 | 6.44e-04 | 0.279 | 0.22200 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 12 | 9.70e-02 | 0.277 | 0.86800 |
| Activation of SMO | 10 | 1.31e-01 | -0.276 | 0.88500 |
| Initiation of Nuclear Envelope (NE) Reformation | 14 | 7.45e-02 | 0.275 | 0.85100 |
| Synthesis of bile acids and bile salts via 27-hydroxycholesterol | 10 | 1.33e-01 | -0.275 | 0.88500 |
| Cleavage of the damaged purine | 10 | 1.35e-01 | 0.273 | 0.88500 |
| Depurination | 10 | 1.35e-01 | 0.273 | 0.88500 |
| Recognition and association of DNA glycosylase with site containing an affected purine | 10 | 1.35e-01 | 0.273 | 0.88500 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 25 | 1.85e-02 | 0.272 | 0.80800 |
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| TRAF6 mediated IRF7 activation | 28 | 1.26e-06 | 5.29e-01 | 0.00168 |
| Condensation of Prophase Chromosomes | 10 | 6.77e-03 | 4.95e-01 | 0.63700 |
| Regulation of IFNA signaling | 23 | 1.21e-04 | 4.63e-01 | 0.08080 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 11 | 9.08e-03 | 4.54e-01 | 0.63700 |
| alpha-linolenic acid (ALA) metabolism | 11 | 9.08e-03 | 4.54e-01 | 0.63700 |
| Heme degradation | 15 | 2.32e-03 | 4.54e-01 | 0.36200 |
| E2F mediated regulation of DNA replication | 18 | 1.09e-03 | 4.45e-01 | 0.29200 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 12 | 1.29e-02 | 4.15e-01 | 0.74800 |
| Regulation of signaling by NODAL | 10 | 4.41e-02 | -3.68e-01 | 0.85100 |
| Regulation of PTEN mRNA translation | 11 | 3.48e-02 | 3.68e-01 | 0.85100 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 12 | 3.16e-02 | 3.58e-01 | 0.85100 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 11 | 4.17e-02 | 3.55e-01 | 0.85100 |
| Tandem pore domain potassium channels | 11 | 4.26e-02 | 3.53e-01 | 0.85100 |
| Scavenging of heme from plasma | 10 | 5.39e-02 | -3.52e-01 | 0.85100 |
| Metabolism of porphyrins | 25 | 2.45e-03 | 3.50e-01 | 0.36200 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 11 | 5.14e-02 | 3.39e-01 | 0.85100 |
| FOXO-mediated transcription of cell death genes | 13 | 3.69e-02 | 3.34e-01 | 0.85100 |
| Citric acid cycle (TCA cycle) | 15 | 2.72e-02 | 3.29e-01 | 0.85100 |
| Cyclin A/B1/B2 associated events during G2/M transition | 13 | 4.04e-02 | 3.28e-01 | 0.85100 |
| Nucleotide-like (purinergic) receptors | 11 | 6.13e-02 | -3.26e-01 | 0.85100 |
| Phase 4 - resting membrane potential | 17 | 2.01e-02 | 3.26e-01 | 0.80800 |
| Diseases associated with the TLR signaling cascade | 18 | 1.89e-02 | -3.20e-01 | 0.80800 |
| Diseases of Immune System | 18 | 1.89e-02 | -3.20e-01 | 0.80800 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 16 | 2.82e-02 | 3.17e-01 | 0.85100 |
| Eicosanoid ligand-binding receptors | 10 | 8.44e-02 | -3.15e-01 | 0.85100 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 13 | 5.13e-02 | 3.12e-01 | 0.85100 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 13 | 5.13e-02 | 3.12e-01 | 0.85100 |
| TP53 Regulates Transcription of Death Receptors and Ligands | 10 | 8.87e-02 | 3.11e-01 | 0.85300 |
| HS-GAG biosynthesis | 22 | 1.24e-02 | -3.08e-01 | 0.74800 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 11 | 8.21e-02 | -3.03e-01 | 0.85100 |
| Defective EXT2 causes exostoses 2 | 11 | 8.21e-02 | -3.03e-01 | 0.85100 |
| Regulation of TP53 Activity through Methylation | 11 | 8.23e-02 | -3.03e-01 | 0.85100 |
| Diseases of DNA repair | 10 | 1.09e-01 | 2.93e-01 | 0.88500 |
| The role of Nef in HIV-1 replication and disease pathogenesis | 23 | 1.55e-02 | 2.91e-01 | 0.76800 |
| ER Quality Control Compartment (ERQC) | 12 | 8.14e-02 | -2.91e-01 | 0.85100 |
| Synthesis of PC | 20 | 2.50e-02 | 2.90e-01 | 0.85100 |
| Defective B4GALT7 causes EDS, progeroid type | 15 | 5.46e-02 | -2.87e-01 | 0.85100 |
| Norepinephrine Neurotransmitter Release Cycle | 12 | 8.78e-02 | -2.85e-01 | 0.85300 |
| Smooth Muscle Contraction | 29 | 8.28e-03 | 2.83e-01 | 0.63700 |
| Heme biosynthesis | 12 | 9.16e-02 | 2.81e-01 | 0.85300 |
| Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 10 | 1.24e-01 | -2.81e-01 | 0.88500 |
| Interferon alpha/beta signaling | 50 | 6.44e-04 | 2.79e-01 | 0.22200 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 12 | 9.70e-02 | 2.77e-01 | 0.86800 |
| Activation of SMO | 10 | 1.31e-01 | -2.76e-01 | 0.88500 |
| Initiation of Nuclear Envelope (NE) Reformation | 14 | 7.45e-02 | 2.75e-01 | 0.85100 |
| Synthesis of bile acids and bile salts via 27-hydroxycholesterol | 10 | 1.33e-01 | -2.75e-01 | 0.88500 |
| Cleavage of the damaged purine | 10 | 1.35e-01 | 2.73e-01 | 0.88500 |
| Depurination | 10 | 1.35e-01 | 2.73e-01 | 0.88500 |
| Recognition and association of DNA glycosylase with site containing an affected purine | 10 | 1.35e-01 | 2.73e-01 | 0.88500 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 25 | 1.85e-02 | 2.72e-01 | 0.80800 |
| Regulation of TLR by endogenous ligand | 13 | 9.12e-02 | -2.71e-01 | 0.85300 |
| eNOS activation | 10 | 1.39e-01 | -2.70e-01 | 0.88500 |
| Insulin receptor recycling | 15 | 7.10e-02 | 2.69e-01 | 0.85100 |
| mTORC1-mediated signalling | 17 | 5.60e-02 | 2.68e-01 | 0.85100 |
| Deadenylation of mRNA | 17 | 5.94e-02 | 2.64e-01 | 0.85100 |
| Phase 2 - plateau phase | 20 | 4.22e-02 | -2.62e-01 | 0.85100 |
| Chondroitin sulfate biosynthesis | 18 | 5.42e-02 | 2.62e-01 | 0.85100 |
| Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane | 11 | 1.36e-01 | 2.60e-01 | 0.88500 |
| Receptor-type tyrosine-protein phosphatases | 14 | 9.40e-02 | -2.59e-01 | 0.85300 |
| Myogenesis | 27 | 2.12e-02 | -2.56e-01 | 0.80800 |
| Glutathione synthesis and recycling | 11 | 1.42e-01 | -2.56e-01 | 0.88500 |
| Telomere Extension By Telomerase | 16 | 7.66e-02 | 2.56e-01 | 0.85100 |
| Transport of vitamins, nucleosides, and related molecules | 36 | 8.93e-03 | 2.52e-01 | 0.63700 |
| Elevation of cytosolic Ca2+ levels | 11 | 1.57e-01 | -2.46e-01 | 0.89700 |
| Depolymerisation of the Nuclear Lamina | 12 | 1.43e-01 | 2.44e-01 | 0.88500 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 11 | 1.63e-01 | 2.43e-01 | 0.89700 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 11 | 1.67e-01 | -2.41e-01 | 0.89700 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | 14 | 1.19e-01 | -2.41e-01 | 0.88500 |
| PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 12 | 1.50e-01 | 2.40e-01 | 0.88800 |
| Defective GALNT12 causes colorectal cancer 1 (CRCS1) | 11 | 1.71e-01 | -2.39e-01 | 0.89700 |
| Apoptotic execution phase | 39 | 1.03e-02 | 2.37e-01 | 0.67900 |
| Activated NOTCH1 Transmits Signal to the Nucleus | 22 | 5.40e-02 | -2.37e-01 | 0.85100 |
| FCERI mediated MAPK activation | 25 | 4.04e-02 | 2.37e-01 | 0.85100 |
| Na+/Cl- dependent neurotransmitter transporters | 14 | 1.29e-01 | 2.34e-01 | 0.88500 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 13 | 1.45e-01 | -2.34e-01 | 0.88500 |
| O-glycosylation of TSR domain-containing proteins | 33 | 2.03e-02 | -2.34e-01 | 0.80800 |
| Pentose phosphate pathway | 10 | 2.02e-01 | -2.33e-01 | 0.89700 |
| Chaperone Mediated Autophagy | 16 | 1.06e-01 | -2.33e-01 | 0.88500 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 14 | 1.32e-01 | -2.33e-01 | 0.88500 |
| Transport of organic anions | 11 | 1.83e-01 | 2.32e-01 | 0.89700 |
| Apoptotic cleavage of cellular proteins | 32 | 2.38e-02 | 2.31e-01 | 0.83500 |
| Defective GALNT3 causes familial hyperphosphatemic tumoral calcinosis (HFTC) | 11 | 1.86e-01 | -2.30e-01 | 0.89700 |
| Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) | 10 | 2.09e-01 | -2.30e-01 | 0.89700 |
| Xenobiotics | 22 | 6.28e-02 | 2.29e-01 | 0.85100 |
| Hyaluronan metabolism | 11 | 1.88e-01 | -2.29e-01 | 0.89700 |
| HDMs demethylate histones | 15 | 1.25e-01 | 2.29e-01 | 0.88500 |
| Glycogen storage diseases | 11 | 1.94e-01 | -2.26e-01 | 0.89700 |
| Regulation of pyruvate dehydrogenase (PDH) complex | 12 | 1.79e-01 | -2.24e-01 | 0.89700 |
| Endogenous sterols | 23 | 6.27e-02 | -2.24e-01 | 0.85100 |
| Defective B3GALTL causes Peters-plus syndrome (PpS) | 32 | 2.85e-02 | -2.24e-01 | 0.85100 |
| Heparan sulfate/heparin (HS-GAG) metabolism | 40 | 1.55e-02 | -2.21e-01 | 0.76800 |
| RNA Polymerase I Transcription Termination | 17 | 1.15e-01 | -2.21e-01 | 0.88500 |
| Syndecan interactions | 16 | 1.27e-01 | -2.20e-01 | 0.88500 |
| Activation of AMPK downstream of NMDARs | 10 | 2.29e-01 | -2.20e-01 | 0.89700 |
| Interleukin-35 Signalling | 11 | 2.09e-01 | 2.19e-01 | 0.89700 |
| Aspartate and asparagine metabolism | 10 | 2.33e-01 | -2.18e-01 | 0.89700 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 22 | 7.73e-02 | 2.18e-01 | 0.85100 |
| Signaling by BMP | 25 | 6.00e-02 | -2.17e-01 | 0.85100 |
| Diseases associated with O-glycosylation of proteins | 53 | 6.32e-03 | -2.17e-01 | 0.63700 |
| Organic cation/anion/zwitterion transport | 13 | 1.77e-01 | 2.16e-01 | 0.89700 |
| TNFs bind their physiological receptors | 20 | 9.43e-02 | 2.16e-01 | 0.85300 |
| HS-GAG degradation | 16 | 1.37e-01 | -2.15e-01 | 0.88500 |
| Activation of RAC1 | 10 | 2.41e-01 | 2.14e-01 | 0.89700 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 12 | 2.03e-01 | 2.12e-01 | 0.89700 |
| Platelet Adhesion to exposed collagen | 11 | 2.25e-01 | 2.11e-01 | 0.89700 |
| Mismatch Repair | 13 | 1.88e-01 | 2.11e-01 | 0.89700 |
| HDR through Single Strand Annealing (SSA) | 26 | 6.28e-02 | -2.11e-01 | 0.85100 |
| Role of phospholipids in phagocytosis | 25 | 6.82e-02 | -2.11e-01 | 0.85100 |
| Beta defensins | 19 | 1.16e-01 | -2.08e-01 | 0.88500 |
| Prolonged ERK activation events | 12 | 2.13e-01 | 2.08e-01 | 0.89700 |
| Aggrephagy | 18 | 1.29e-01 | -2.07e-01 | 0.88500 |
| Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS) | 12 | 2.15e-01 | -2.07e-01 | 0.89700 |
| Ribosomal scanning and start codon recognition | 21 | 1.02e-01 | 2.06e-01 | 0.87300 |
| Translation initiation complex formation | 21 | 1.02e-01 | 2.06e-01 | 0.87300 |
| Mitochondrial calcium ion transport | 17 | 1.41e-01 | 2.06e-01 | 0.88500 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 59 | 6.27e-03 | 2.06e-01 | 0.63700 |
| Activation of BAD and translocation to mitochondria | 14 | 1.86e-01 | 2.04e-01 | 0.89700 |
| The canonical retinoid cycle in rods (twilight vision) | 19 | 1.25e-01 | -2.04e-01 | 0.88500 |
| Meiotic synapsis | 29 | 5.82e-02 | 2.03e-01 | 0.85100 |
| Striated Muscle Contraction | 32 | 4.69e-02 | -2.03e-01 | 0.85100 |
| Late endosomal microautophagy | 22 | 1.01e-01 | -2.02e-01 | 0.87300 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 19 | 1.29e-01 | 2.01e-01 | 0.88500 |
| RHO GTPases activate PKNs | 27 | 7.20e-02 | 2.00e-01 | 0.85100 |
| A tetrasaccharide linker sequence is required for GAG synthesis | 20 | 1.23e-01 | -1.99e-01 | 0.88500 |
| PCNA-Dependent Long Patch Base Excision Repair | 15 | 1.84e-01 | 1.98e-01 | 0.89700 |
| Mitotic Prophase | 61 | 7.66e-03 | 1.98e-01 | 0.63700 |
| TRAF3-dependent IRF activation pathway | 14 | 2.02e-01 | 1.97e-01 | 0.89700 |
| Diseases of programmed cell death | 18 | 1.51e-01 | 1.96e-01 | 0.88800 |
| RAS processing | 13 | 2.25e-01 | 1.95e-01 | 0.89700 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 17 | 1.66e-01 | 1.94e-01 | 0.89700 |
| Metalloprotease DUBs | 16 | 1.80e-01 | 1.94e-01 | 0.89700 |
| N-glycan antennae elongation in the medial/trans-Golgi | 19 | 1.45e-01 | -1.93e-01 | 0.88500 |
| Regulation of gene expression in beta cells | 14 | 2.11e-01 | -1.93e-01 | 0.89700 |
| NOTCH4 Intracellular Domain Regulates Transcription | 18 | 1.57e-01 | 1.93e-01 | 0.89700 |
| RHO GTPases Activate WASPs and WAVEs | 30 | 6.81e-02 | 1.93e-01 | 0.85100 |
| PI3K Cascade | 38 | 4.02e-02 | -1.92e-01 | 0.85100 |
| Metabolic disorders of biological oxidation enzymes | 29 | 7.32e-02 | -1.92e-01 | 0.85100 |
| Interleukin-12 family signaling | 41 | 3.42e-02 | 1.91e-01 | 0.85100 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 13 | 2.33e-01 | 1.91e-01 | 0.89700 |
| Nuclear Envelope (NE) Reassembly | 56 | 1.38e-02 | 1.90e-01 | 0.76400 |
| Synthesis of IP3 and IP4 in the cytosol | 22 | 1.25e-01 | 1.89e-01 | 0.88500 |
| Presynaptic phase of homologous DNA pairing and strand exchange | 25 | 1.02e-01 | -1.89e-01 | 0.87300 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 12 | 2.58e-01 | 1.89e-01 | 0.89700 |
| GAB1 signalosome | 14 | 2.23e-01 | -1.88e-01 | 0.89700 |
| Fertilization | 19 | 1.58e-01 | -1.87e-01 | 0.89700 |
| Metabolism of steroid hormones | 29 | 8.15e-02 | -1.87e-01 | 0.85100 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 50 | 2.24e-02 | 1.87e-01 | 0.80800 |
| Nonsense-Mediated Decay (NMD) | 50 | 2.24e-02 | 1.87e-01 | 0.80800 |
| CD28 dependent PI3K/Akt signaling | 20 | 1.50e-01 | -1.86e-01 | 0.88800 |
| FCERI mediated Ca+2 mobilization | 24 | 1.15e-01 | 1.86e-01 | 0.88500 |
| Signalling to ERKs | 30 | 7.91e-02 | 1.85e-01 | 0.85100 |
| Pyruvate metabolism | 23 | 1.25e-01 | -1.85e-01 | 0.88500 |
| Processing of Capped Intronless Pre-mRNA | 17 | 1.88e-01 | 1.85e-01 | 0.89700 |
| Signaling by NODAL | 18 | 1.77e-01 | -1.84e-01 | 0.89700 |
| G1/S-Specific Transcription | 24 | 1.19e-01 | 1.84e-01 | 0.88500 |
| N-Glycan antennae elongation | 12 | 2.71e-01 | -1.84e-01 | 0.89800 |
| Deactivation of the beta-catenin transactivating complex | 28 | 9.28e-02 | -1.84e-01 | 0.85300 |
| Transcription of E2F targets under negative control by DREAM complex | 16 | 2.04e-01 | 1.83e-01 | 0.89700 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 13 | 2.56e-01 | -1.82e-01 | 0.89700 |
| Triglyceride catabolism | 18 | 1.82e-01 | -1.82e-01 | 0.89700 |
| Termination of O-glycan biosynthesis | 17 | 1.95e-01 | -1.82e-01 | 0.89700 |
| Neurexins and neuroligins | 50 | 2.65e-02 | -1.82e-01 | 0.85100 |
| Transferrin endocytosis and recycling | 20 | 1.60e-01 | 1.81e-01 | 0.89700 |
| RNA Polymerase I Transcription Initiation | 30 | 8.67e-02 | -1.81e-01 | 0.85300 |
| Antimicrobial peptides | 45 | 3.61e-02 | -1.81e-01 | 0.85100 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 12 | 2.79e-01 | 1.81e-01 | 0.90400 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 10 | 3.23e-01 | -1.81e-01 | 0.92900 |
| Incretin synthesis, secretion, and inactivation | 16 | 2.14e-01 | -1.80e-01 | 0.89700 |
| Cyclin D associated events in G1 | 32 | 7.90e-02 | 1.80e-01 | 0.85100 |
| G1 Phase | 32 | 7.90e-02 | 1.80e-01 | 0.85100 |
| Selective autophagy | 47 | 3.35e-02 | -1.79e-01 | 0.85100 |
| Fatty acyl-CoA biosynthesis | 27 | 1.07e-01 | 1.79e-01 | 0.88500 |
| Regulation of Complement cascade | 38 | 5.65e-02 | -1.79e-01 | 0.85100 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 19 | 1.79e-01 | -1.78e-01 | 0.89700 |
| PERK regulates gene expression | 20 | 1.71e-01 | 1.77e-01 | 0.89700 |
| Signal transduction by L1 | 15 | 2.36e-01 | 1.77e-01 | 0.89700 |
| Biosynthesis of DHA-derived SPMs | 14 | 2.52e-01 | 1.77e-01 | 0.89700 |
| Interleukin-12 signaling | 32 | 8.49e-02 | 1.76e-01 | 0.85100 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | 13 | 2.74e-01 | 1.75e-01 | 0.89800 |
| Diseases of hemostasis | 13 | 2.74e-01 | 1.75e-01 | 0.89800 |
| Defensins | 20 | 1.76e-01 | -1.75e-01 | 0.89700 |
| Signalling to RAS | 17 | 2.12e-01 | 1.75e-01 | 0.89700 |
| Intrinsic Pathway of Fibrin Clot Formation | 18 | 2.01e-01 | 1.74e-01 | 0.89700 |
| Budding and maturation of HIV virion | 17 | 2.16e-01 | -1.73e-01 | 0.89700 |
| Mitochondrial tRNA aminoacylation | 12 | 2.99e-01 | -1.73e-01 | 0.91700 |
| Methylation | 10 | 3.44e-01 | -1.73e-01 | 0.92900 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | 17 | 2.18e-01 | 1.73e-01 | 0.89700 |
| Neurodegenerative Diseases | 17 | 2.18e-01 | 1.73e-01 | 0.89700 |
| MicroRNA (miRNA) biogenesis | 13 | 2.82e-01 | -1.73e-01 | 0.90400 |
| Metabolism of nitric oxide: NOS3 activation and regulation | 14 | 2.64e-01 | -1.72e-01 | 0.89800 |
| Constitutive Signaling by EGFRvIII | 13 | 2.84e-01 | 1.72e-01 | 0.90400 |
| Signaling by EGFRvIII in Cancer | 13 | 2.84e-01 | 1.72e-01 | 0.90400 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | 22 | 1.66e-01 | -1.71e-01 | 0.89700 |
| Defective B3GAT3 causes JDSSDHD | 15 | 2.53e-01 | -1.71e-01 | 0.89700 |
| Arachidonic acid metabolism | 46 | 4.64e-02 | 1.70e-01 | 0.85100 |
| RNA Polymerase II Transcription Termination | 46 | 4.65e-02 | 1.70e-01 | 0.85100 |
| Mitochondrial protein import | 45 | 4.91e-02 | -1.70e-01 | 0.85100 |
| HIV elongation arrest and recovery | 15 | 2.56e-01 | -1.69e-01 | 0.89700 |
| Pausing and recovery of HIV elongation | 15 | 2.56e-01 | -1.69e-01 | 0.89700 |
| Pausing and recovery of Tat-mediated HIV elongation | 15 | 2.56e-01 | -1.69e-01 | 0.89700 |
| Tat-mediated HIV elongation arrest and recovery | 15 | 2.56e-01 | -1.69e-01 | 0.89700 |
| Carnitine metabolism | 11 | 3.31e-01 | -1.69e-01 | 0.92900 |
| Cell surface interactions at the vascular wall | 114 | 1.89e-03 | -1.69e-01 | 0.35900 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 11 | 3.34e-01 | 1.68e-01 | 0.92900 |
| Activation of gene expression by SREBF (SREBP) | 35 | 8.61e-02 | 1.68e-01 | 0.85300 |
| Insulin processing | 17 | 2.36e-01 | 1.66e-01 | 0.89700 |
| Kinesins | 34 | 9.47e-02 | -1.66e-01 | 0.85300 |
| Glucagon-type ligand receptors | 25 | 1.53e-01 | 1.65e-01 | 0.89100 |
| Homologous DNA Pairing and Strand Exchange | 28 | 1.31e-01 | -1.65e-01 | 0.88500 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 46 | 5.33e-02 | -1.65e-01 | 0.85100 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants | 11 | 3.45e-01 | -1.65e-01 | 0.92900 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer | 11 | 3.45e-01 | -1.65e-01 | 0.92900 |
| ATF4 activates genes in response to endoplasmic reticulum stress | 17 | 2.40e-01 | 1.64e-01 | 0.89700 |
| Protein-protein interactions at synapses | 73 | 1.53e-02 | -1.64e-01 | 0.76800 |
| FGFR4 ligand binding and activation | 11 | 3.46e-01 | -1.64e-01 | 0.92900 |
| Generation of second messenger molecules | 23 | 1.75e-01 | 1.63e-01 | 0.89700 |
| Basigin interactions | 23 | 1.77e-01 | -1.63e-01 | 0.89700 |
| Lysine catabolism | 11 | 3.54e-01 | 1.62e-01 | 0.93100 |
| IGF1R signaling cascade | 45 | 6.10e-02 | -1.62e-01 | 0.85100 |
| Translesion Synthesis by POLH | 11 | 3.54e-01 | 1.61e-01 | 0.93100 |
| Activation of Matrix Metalloproteinases | 23 | 1.82e-01 | -1.61e-01 | 0.89700 |
| Plasma lipoprotein assembly | 12 | 3.35e-01 | -1.61e-01 | 0.92900 |
| VEGFR2 mediated vascular permeability | 25 | 1.66e-01 | -1.60e-01 | 0.89700 |
| Regulation of necroptotic cell death | 12 | 3.37e-01 | 1.60e-01 | 0.92900 |
| SUMOylation of DNA replication proteins | 32 | 1.18e-01 | 1.60e-01 | 0.88500 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | 24 | 1.76e-01 | 1.60e-01 | 0.89700 |
| SARS-CoV-1 Infection | 32 | 1.18e-01 | 1.60e-01 | 0.88500 |
| mRNA 3'-end processing | 40 | 8.38e-02 | 1.58e-01 | 0.85100 |
| Negative epigenetic regulation of rRNA expression | 29 | 1.42e-01 | -1.58e-01 | 0.88500 |
| p38MAPK events | 12 | 3.46e-01 | 1.57e-01 | 0.92900 |
| Pyrimidine catabolism | 10 | 3.90e-01 | 1.57e-01 | 0.94500 |
| DARPP-32 events | 20 | 2.25e-01 | 1.57e-01 | 0.89700 |
| Regulation of KIT signaling | 11 | 3.69e-01 | 1.56e-01 | 0.94500 |
| Gluconeogenesis | 28 | 1.53e-01 | -1.56e-01 | 0.89100 |
| Formation of tubulin folding intermediates by CCT/TriC | 19 | 2.40e-01 | 1.56e-01 | 0.89700 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 25 | 1.79e-01 | 1.55e-01 | 0.89700 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 36 | 1.08e-01 | 1.55e-01 | 0.88500 |
| Cell recruitment (pro-inflammatory response) | 19 | 2.44e-01 | -1.55e-01 | 0.89700 |
| Purinergic signaling in leishmaniasis infection | 19 | 2.44e-01 | -1.55e-01 | 0.89700 |
| IRS-mediated signalling | 41 | 8.72e-02 | -1.54e-01 | 0.85300 |
| Passive transport by Aquaporins | 12 | 3.54e-01 | -1.54e-01 | 0.93100 |
| Frs2-mediated activation | 10 | 4.00e-01 | 1.54e-01 | 0.94500 |
| Resolution of D-Loop Structures | 23 | 2.02e-01 | -1.54e-01 | 0.89700 |
| Serotonin Neurotransmitter Release Cycle | 11 | 3.79e-01 | -1.53e-01 | 0.94500 |
| ECM proteoglycans | 47 | 6.97e-02 | -1.53e-01 | 0.85100 |
| Post-chaperonin tubulin folding pathway | 20 | 2.37e-01 | 1.53e-01 | 0.89700 |
| NOTCH2 intracellular domain regulates transcription | 10 | 4.03e-01 | 1.53e-01 | 0.94500 |
| Acyl chain remodelling of PS | 16 | 2.91e-01 | -1.53e-01 | 0.90700 |
| tRNA Aminoacylation | 17 | 2.77e-01 | -1.52e-01 | 0.90000 |
| Signaling by cytosolic FGFR1 fusion mutants | 16 | 2.92e-01 | 1.52e-01 | 0.90700 |
| RIPK1-mediated regulated necrosis | 14 | 3.26e-01 | 1.52e-01 | 0.92900 |
| Regulated Necrosis | 14 | 3.26e-01 | 1.52e-01 | 0.92900 |
| CD28 dependent Vav1 pathway | 11 | 3.84e-01 | 1.52e-01 | 0.94500 |
| Glyoxylate metabolism and glycine degradation | 26 | 1.82e-01 | -1.51e-01 | 0.89700 |
| Transport of Mature Transcript to Cytoplasm | 60 | 4.31e-02 | 1.51e-01 | 0.85100 |
| Digestion and absorption | 21 | 2.32e-01 | -1.51e-01 | 0.89700 |
| IRS-related events triggered by IGF1R | 44 | 8.39e-02 | -1.51e-01 | 0.85100 |
| Processing of Intronless Pre-mRNAs | 11 | 3.87e-01 | 1.51e-01 | 0.94500 |
| Glycogen synthesis | 11 | 3.89e-01 | -1.50e-01 | 0.94500 |
| PECAM1 interactions | 10 | 4.12e-01 | 1.50e-01 | 0.94500 |
| Formation of the cornified envelope | 31 | 1.50e-01 | -1.50e-01 | 0.88800 |
| G0 and Early G1 | 22 | 2.26e-01 | 1.49e-01 | 0.89700 |
| Assembly of collagen fibrils and other multimeric structures | 45 | 8.37e-02 | -1.49e-01 | 0.85100 |
| Postmitotic nuclear pore complex (NPC) reformation | 20 | 2.50e-01 | 1.49e-01 | 0.89700 |
| Protein ubiquitination | 38 | 1.14e-01 | 1.48e-01 | 0.88500 |
| MAPK targets/ Nuclear events mediated by MAP kinases | 26 | 1.91e-01 | 1.48e-01 | 0.89700 |
| NoRC negatively regulates rRNA expression | 26 | 1.93e-01 | -1.48e-01 | 0.89700 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 44 | 9.08e-02 | 1.47e-01 | 0.85300 |
| Metabolism of non-coding RNA | 34 | 1.37e-01 | 1.47e-01 | 0.88500 |
| snRNP Assembly | 34 | 1.37e-01 | 1.47e-01 | 0.88500 |
| Effects of PIP2 hydrolysis | 20 | 2.57e-01 | -1.46e-01 | 0.89700 |
| Eukaryotic Translation Elongation | 37 | 1.25e-01 | 1.46e-01 | 0.88500 |
| Signaling by ERBB2 ECD mutants | 14 | 3.46e-01 | 1.45e-01 | 0.92900 |
| KSRP (KHSRP) binds and destabilizes mRNA | 13 | 3.64e-01 | 1.45e-01 | 0.94300 |
| FGFRL1 modulation of FGFR1 signaling | 12 | 3.84e-01 | 1.45e-01 | 0.94500 |
| Role of LAT2/NTAL/LAB on calcium mobilization | 13 | 3.67e-01 | 1.45e-01 | 0.94500 |
| Gastrin-CREB signalling pathway via PKC and MAPK | 16 | 3.18e-01 | 1.44e-01 | 0.92900 |
| Non-integrin membrane-ECM interactions | 35 | 1.40e-01 | -1.44e-01 | 0.88500 |
| Oncogene Induced Senescence | 25 | 2.14e-01 | 1.44e-01 | 0.89700 |
| Peptide chain elongation | 34 | 1.48e-01 | 1.44e-01 | 0.88800 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 54 | 6.92e-02 | 1.43e-01 | 0.85100 |
| mRNA decay by 3' to 5' exoribonuclease | 10 | 4.34e-01 | 1.43e-01 | 0.94500 |
| TRP channels | 20 | 2.70e-01 | -1.43e-01 | 0.89800 |
| Spry regulation of FGF signaling | 11 | 4.13e-01 | 1.43e-01 | 0.94500 |
| Sema3A PAK dependent Axon repulsion | 12 | 3.95e-01 | 1.42e-01 | 0.94500 |
| SUMOylation of DNA damage response and repair proteins | 50 | 8.34e-02 | 1.42e-01 | 0.85100 |
| CD209 (DC-SIGN) signaling | 18 | 3.00e-01 | 1.41e-01 | 0.91700 |
| Keratan sulfate biosynthesis | 21 | 2.63e-01 | 1.41e-01 | 0.89800 |
| Complement cascade | 48 | 9.11e-02 | -1.41e-01 | 0.85300 |
| Selenocysteine synthesis | 36 | 1.44e-01 | 1.41e-01 | 0.88500 |
| NCAM1 interactions | 30 | 1.84e-01 | -1.40e-01 | 0.89700 |
| Biosynthesis of specialized proresolving mediators (SPMs) | 16 | 3.34e-01 | 1.40e-01 | 0.92900 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 45 | 1.06e-01 | 1.39e-01 | 0.88500 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 24 | 2.41e-01 | 1.38e-01 | 0.89700 |
| G alpha (12/13) signalling events | 65 | 5.50e-02 | -1.38e-01 | 0.85100 |
| Regulation of signaling by CBL | 15 | 3.56e-01 | 1.38e-01 | 0.93100 |
| Signaling by RAF1 mutants | 31 | 1.87e-01 | 1.37e-01 | 0.89700 |
| Interferon Signaling | 133 | 6.48e-03 | 1.37e-01 | 0.63700 |
| RORA activates gene expression | 16 | 3.44e-01 | 1.37e-01 | 0.92900 |
| TGF-beta receptor signaling activates SMADs | 19 | 3.03e-01 | -1.37e-01 | 0.91800 |
| NEP/NS2 Interacts with the Cellular Export Machinery | 22 | 2.68e-01 | 1.37e-01 | 0.89800 |
| Synthesis of very long-chain fatty acyl-CoAs | 19 | 3.03e-01 | 1.36e-01 | 0.91800 |
| Regulation of TP53 Activity through Association with Co-factors | 12 | 4.16e-01 | 1.36e-01 | 0.94500 |
| Iron uptake and transport | 41 | 1.33e-01 | 1.36e-01 | 0.88500 |
| SUMOylation of SUMOylation proteins | 22 | 2.72e-01 | 1.35e-01 | 0.89800 |
| Base Excision Repair | 37 | 1.55e-01 | 1.35e-01 | 0.89700 |
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) | 11 | 4.40e-01 | 1.34e-01 | 0.94500 |
| Meiosis | 46 | 1.16e-01 | 1.34e-01 | 0.88500 |
| ERKs are inactivated | 11 | 4.43e-01 | 1.34e-01 | 0.94500 |
| Sema4D in semaphorin signaling | 19 | 3.16e-01 | -1.33e-01 | 0.92900 |
| Rev-mediated nuclear export of HIV RNA | 24 | 2.60e-01 | 1.33e-01 | 0.89800 |
| NGF-stimulated transcription | 32 | 1.94e-01 | 1.33e-01 | 0.89700 |
| RUNX2 regulates osteoblast differentiation | 18 | 3.29e-01 | 1.33e-01 | 0.92900 |
| Positive epigenetic regulation of rRNA expression | 32 | 1.96e-01 | -1.32e-01 | 0.89700 |
| O-linked glycosylation | 85 | 3.59e-02 | -1.32e-01 | 0.85100 |
| Metabolism of amine-derived hormones | 15 | 3.77e-01 | -1.32e-01 | 0.94500 |
| Prefoldin mediated transfer of substrate to CCT/TriC | 21 | 2.96e-01 | 1.32e-01 | 0.91600 |
| Binding and Uptake of Ligands by Scavenger Receptors | 33 | 1.90e-01 | -1.32e-01 | 0.89700 |
| Vpr-mediated nuclear import of PICs | 23 | 2.76e-01 | 1.31e-01 | 0.89900 |
| Transport of bile salts and organic acids, metal ions and amine compounds | 65 | 6.77e-02 | 1.31e-01 | 0.85100 |
| Class I peroxisomal membrane protein import | 11 | 4.52e-01 | -1.31e-01 | 0.94500 |
| RNA Polymerase I Promoter Escape | 17 | 3.50e-01 | -1.31e-01 | 0.93100 |
| Formation of the ternary complex, and subsequently, the 43S complex | 18 | 3.37e-01 | 1.31e-01 | 0.92900 |
| Recycling pathway of L1 | 24 | 2.68e-01 | 1.31e-01 | 0.89800 |
| Transcriptional Regulation by E2F6 | 27 | 2.40e-01 | 1.31e-01 | 0.89700 |
| mRNA decay by 5' to 3' exoribonuclease | 12 | 4.33e-01 | -1.31e-01 | 0.94500 |
| Regulation of PLK1 Activity at G2/M Transition | 63 | 7.40e-02 | 1.30e-01 | 0.85100 |
| Caspase-mediated cleavage of cytoskeletal proteins | 10 | 4.76e-01 | 1.30e-01 | 0.94500 |
| Extracellular matrix organization | 234 | 6.65e-04 | -1.30e-01 | 0.22200 |
| Transport of Mature mRNA Derived from an Intronless Transcript | 28 | 2.37e-01 | 1.29e-01 | 0.89700 |
| Synaptic adhesion-like molecules | 18 | 3.45e-01 | -1.29e-01 | 0.92900 |
| Interleukin-7 signaling | 14 | 4.07e-01 | -1.28e-01 | 0.94500 |
| MHC class II antigen presentation | 86 | 4.08e-02 | -1.28e-01 | 0.85100 |
| Antigen processing-Cross presentation | 68 | 6.95e-02 | -1.27e-01 | 0.85100 |
| SARS-CoV Infections | 58 | 9.40e-02 | 1.27e-01 | 0.85300 |
| Class C/3 (Metabotropic glutamate/pheromone receptors) | 18 | 3.51e-01 | 1.27e-01 | 0.93100 |
| Purine salvage | 11 | 4.66e-01 | 1.27e-01 | 0.94500 |
| Collagen formation | 70 | 6.76e-02 | -1.26e-01 | 0.85100 |
| Nuclear signaling by ERBB4 | 25 | 2.75e-01 | -1.26e-01 | 0.89800 |
| PKA-mediated phosphorylation of CREB | 16 | 3.84e-01 | 1.26e-01 | 0.94500 |
| Regulation of RUNX1 Expression and Activity | 14 | 4.16e-01 | 1.26e-01 | 0.94500 |
| PI-3K cascade:FGFR4 | 17 | 3.70e-01 | -1.25e-01 | 0.94500 |
| Lewis blood group biosynthesis | 10 | 4.92e-01 | -1.25e-01 | 0.94500 |
| Class B/2 (Secretin family receptors) | 72 | 6.65e-02 | 1.25e-01 | 0.85100 |
| SUMOylation of intracellular receptors | 26 | 2.69e-01 | 1.25e-01 | 0.89800 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | 29 | 2.44e-01 | 1.25e-01 | 0.89700 |
| Translation of structural proteins | 19 | 3.46e-01 | 1.25e-01 | 0.92900 |
| Sphingolipid de novo biosynthesis | 32 | 2.22e-01 | 1.25e-01 | 0.89700 |
| Transcriptional regulation of white adipocyte differentiation | 67 | 7.82e-02 | 1.25e-01 | 0.85100 |
| COPI-dependent Golgi-to-ER retrograde traffic | 62 | 9.07e-02 | -1.24e-01 | 0.85300 |
| Antiviral mechanism by IFN-stimulated genes | 55 | 1.12e-01 | 1.24e-01 | 0.88500 |
| Phospholipase C-mediated cascade; FGFR4 | 12 | 4.57e-01 | -1.24e-01 | 0.94500 |
| Nuclear Events (kinase and transcription factor activation) | 51 | 1.26e-01 | 1.24e-01 | 0.88500 |
| ISG15 antiviral mechanism | 49 | 1.37e-01 | 1.23e-01 | 0.88500 |
| Regulation of innate immune responses to cytosolic DNA | 11 | 4.82e-01 | -1.22e-01 | 0.94500 |
| MAP2K and MAPK activation | 29 | 2.54e-01 | 1.22e-01 | 0.89700 |
| Regulation of TP53 Activity through Phosphorylation | 67 | 8.43e-02 | -1.22e-01 | 0.85100 |
| Retinoid metabolism and transport | 30 | 2.50e-01 | -1.21e-01 | 0.89700 |
| MECP2 regulates neuronal receptors and channels | 14 | 4.31e-01 | -1.21e-01 | 0.94500 |
| Glutamate and glutamine metabolism | 13 | 4.48e-01 | -1.21e-01 | 0.94500 |
| Plasma lipoprotein remodeling | 23 | 3.14e-01 | -1.21e-01 | 0.92900 |
| EPHA-mediated growth cone collapse | 12 | 4.67e-01 | 1.21e-01 | 0.94500 |
| XBP1(S) activates chaperone genes | 38 | 1.97e-01 | -1.21e-01 | 0.89700 |
| Synthesis of glycosylphosphatidylinositol (GPI) | 12 | 4.68e-01 | 1.21e-01 | 0.94500 |
| Interactions of Rev with host cellular proteins | 25 | 2.96e-01 | 1.21e-01 | 0.91600 |
| Regulation of TP53 Activity through Acetylation | 23 | 3.16e-01 | -1.21e-01 | 0.92900 |
| Platelet sensitization by LDL | 15 | 4.20e-01 | -1.20e-01 | 0.94500 |
| Amino acids regulate mTORC1 | 36 | 2.12e-01 | 1.20e-01 | 0.89700 |
| Response of Mtb to phagocytosis | 18 | 3.78e-01 | 1.20e-01 | 0.94500 |
| Signaling by PDGFRA extracellular domain mutants | 11 | 4.91e-01 | 1.20e-01 | 0.94500 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 11 | 4.91e-01 | 1.20e-01 | 0.94500 |
| Signaling by WNT in cancer | 27 | 2.81e-01 | -1.20e-01 | 0.90400 |
| Signaling by Activin | 12 | 4.72e-01 | 1.20e-01 | 0.94500 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 11 | 4.93e-01 | 1.19e-01 | 0.94500 |
| RNA Polymerase I Promoter Clearance | 33 | 2.35e-01 | -1.19e-01 | 0.89700 |
| Transport of Ribonucleoproteins into the Host Nucleus | 22 | 3.33e-01 | 1.19e-01 | 0.92900 |
| Surfactant metabolism | 20 | 3.59e-01 | -1.18e-01 | 0.93400 |
| DNA Damage/Telomere Stress Induced Senescence | 21 | 3.48e-01 | 1.18e-01 | 0.93100 |
| CLEC7A (Dectin-1) induces NFAT activation | 10 | 5.18e-01 | 1.18e-01 | 0.94500 |
| Circadian Clock | 56 | 1.27e-01 | 1.18e-01 | 0.88500 |
| Glutamate Neurotransmitter Release Cycle | 19 | 3.75e-01 | -1.18e-01 | 0.94500 |
| CASP8 activity is inhibited | 10 | 5.21e-01 | 1.17e-01 | 0.94500 |
| Dimerization of procaspase-8 | 10 | 5.21e-01 | 1.17e-01 | 0.94500 |
| Regulation by c-FLIP | 10 | 5.21e-01 | 1.17e-01 | 0.94500 |
| Diseases associated with visual transduction | 11 | 5.05e-01 | 1.16e-01 | 0.94500 |
| Diseases of the neuronal system | 11 | 5.05e-01 | 1.16e-01 | 0.94500 |
| Retinoid cycle disease events | 11 | 5.05e-01 | 1.16e-01 | 0.94500 |
| Acetylcholine Neurotransmitter Release Cycle | 11 | 5.05e-01 | -1.16e-01 | 0.94500 |
| Diseases of glycosylation | 114 | 3.31e-02 | -1.16e-01 | 0.85100 |
| Extension of Telomeres | 36 | 2.30e-01 | 1.16e-01 | 0.89700 |
| Sulfur amino acid metabolism | 21 | 3.59e-01 | -1.16e-01 | 0.93400 |
| Transcriptional regulation of granulopoiesis | 29 | 2.82e-01 | 1.15e-01 | 0.90400 |
| G1/S Transition | 94 | 5.41e-02 | 1.15e-01 | 0.85100 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | 12 | 4.90e-01 | 1.15e-01 | 0.94500 |
| RHO GTPases activate CIT | 16 | 4.26e-01 | 1.15e-01 | 0.94500 |
| Export of Viral Ribonucleoproteins from Nucleus | 23 | 3.42e-01 | 1.14e-01 | 0.92900 |
| Resolution of Sister Chromatid Cohesion | 78 | 8.14e-02 | 1.14e-01 | 0.85100 |
| SRP-dependent cotranslational protein targeting to membrane | 49 | 1.67e-01 | 1.14e-01 | 0.89700 |
| RAF-independent MAPK1/3 activation | 18 | 4.03e-01 | 1.14e-01 | 0.94500 |
| PRC2 methylates histones and DNA | 11 | 5.16e-01 | 1.13e-01 | 0.94500 |
| Mitotic G2-G2/M phases | 131 | 2.59e-02 | 1.13e-01 | 0.85100 |
| Signaling by FGFR1 in disease | 32 | 2.69e-01 | 1.13e-01 | 0.89800 |
| Formation of a pool of free 40S subunits | 40 | 2.18e-01 | 1.13e-01 | 0.89700 |
| FGFR2c ligand binding and activation | 10 | 5.38e-01 | -1.13e-01 | 0.94500 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | 43 | 2.02e-01 | 1.12e-01 | 0.89700 |
| SUMOylation of ubiquitinylation proteins | 26 | 3.24e-01 | 1.12e-01 | 0.92900 |
| Translocation of ZAP-70 to Immunological synapse | 12 | 5.03e-01 | 1.12e-01 | 0.94500 |
| Deadenylation-dependent mRNA decay | 39 | 2.27e-01 | 1.12e-01 | 0.89700 |
| AURKA Activation by TPX2 | 57 | 1.45e-01 | 1.12e-01 | 0.88500 |
| Golgi-to-ER retrograde transport | 89 | 6.98e-02 | -1.11e-01 | 0.85100 |
| Intraflagellar transport | 36 | 2.49e-01 | -1.11e-01 | 0.89700 |
| MET activates PTK2 signaling | 16 | 4.43e-01 | -1.11e-01 | 0.94500 |
| Sialic acid metabolism | 27 | 3.19e-01 | -1.11e-01 | 0.92900 |
| Tight junction interactions | 26 | 3.29e-01 | -1.11e-01 | 0.92900 |
| Calnexin/calreticulin cycle | 15 | 4.59e-01 | -1.10e-01 | 0.94500 |
| WNT5A-dependent internalization of FZD4 | 12 | 5.09e-01 | 1.10e-01 | 0.94500 |
| DNA Damage Bypass | 32 | 2.82e-01 | 1.10e-01 | 0.90400 |
| Adherens junctions interactions | 19 | 4.07e-01 | -1.10e-01 | 0.94500 |
| Cap-dependent Translation Initiation | 51 | 1.75e-01 | 1.10e-01 | 0.89700 |
| Eukaryotic Translation Initiation | 51 | 1.75e-01 | 1.10e-01 | 0.89700 |
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 18 | 4.20e-01 | -1.10e-01 | 0.94500 |
| Downstream signal transduction | 26 | 3.34e-01 | 1.10e-01 | 0.92900 |
| Signaling by Erythropoietin | 21 | 3.85e-01 | 1.09e-01 | 0.94500 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 19 | 4.10e-01 | -1.09e-01 | 0.94500 |
| Synthesis of PIPs at the plasma membrane | 48 | 1.91e-01 | 1.09e-01 | 0.89700 |
| Regulation of MECP2 expression and activity | 23 | 3.66e-01 | 1.09e-01 | 0.94500 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 12 | 5.14e-01 | 1.09e-01 | 0.94500 |
| Cargo concentration in the ER | 22 | 3.77e-01 | -1.09e-01 | 0.94500 |
| Free fatty acids regulate insulin secretion | 11 | 5.32e-01 | -1.09e-01 | 0.94500 |
| Deubiquitination | 186 | 1.07e-02 | 1.09e-01 | 0.67900 |
| ERK/MAPK targets | 19 | 4.13e-01 | 1.08e-01 | 0.94500 |
| Regulation of expression of SLITs and ROBOs | 90 | 7.64e-02 | 1.08e-01 | 0.85100 |
| The NLRP3 inflammasome | 11 | 5.35e-01 | -1.08e-01 | 0.94500 |
| Glucagon signaling in metabolic regulation | 25 | 3.51e-01 | 1.08e-01 | 0.93100 |
| Signaling by PDGFR in disease | 18 | 4.29e-01 | 1.08e-01 | 0.94500 |
| Prolactin receptor signaling | 13 | 5.02e-01 | 1.07e-01 | 0.94500 |
| Golgi Associated Vesicle Biogenesis | 40 | 2.40e-01 | 1.07e-01 | 0.89700 |
| Regulation of RUNX3 expression and activity | 38 | 2.56e-01 | -1.07e-01 | 0.89700 |
| p75NTR signals via NF-kB | 10 | 5.61e-01 | -1.06e-01 | 0.94500 |
| Nephrin family interactions | 19 | 4.24e-01 | 1.06e-01 | 0.94500 |
| G2/M Transition | 129 | 3.82e-02 | 1.06e-01 | 0.85100 |
| Assembly of active LPL and LIPC lipase complexes | 16 | 4.64e-01 | -1.06e-01 | 0.94500 |
| Amyloid fiber formation | 35 | 2.80e-01 | 1.06e-01 | 0.90400 |
| Viral mRNA Translation | 34 | 2.87e-01 | 1.06e-01 | 0.90700 |
| Activation of Ca-permeable Kainate Receptor | 10 | 5.63e-01 | -1.06e-01 | 0.94500 |
| Ionotropic activity of kainate receptors | 10 | 5.63e-01 | -1.06e-01 | 0.94500 |
| Integrin cell surface interactions | 56 | 1.75e-01 | -1.05e-01 | 0.89700 |
| Activation of HOX genes during differentiation | 41 | 2.46e-01 | 1.05e-01 | 0.89700 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 41 | 2.46e-01 | 1.05e-01 | 0.89700 |
| Transcriptional activation of mitochondrial biogenesis | 45 | 2.25e-01 | 1.05e-01 | 0.89700 |
| Degradation of the extracellular matrix | 84 | 9.78e-02 | -1.05e-01 | 0.86900 |
| O-linked glycosylation of mucins | 48 | 2.10e-01 | -1.05e-01 | 0.89700 |
| Phase I - Functionalization of compounds | 84 | 9.85e-02 | 1.04e-01 | 0.86900 |
| Other interleukin signaling | 17 | 4.57e-01 | -1.04e-01 | 0.94500 |
| Platelet Aggregation (Plug Formation) | 33 | 3.00e-01 | 1.04e-01 | 0.91700 |
| Synthesis of PA | 29 | 3.32e-01 | -1.04e-01 | 0.92900 |
| Signaling by Non-Receptor Tyrosine Kinases | 41 | 2.50e-01 | 1.04e-01 | 0.89700 |
| Signaling by PTK6 | 41 | 2.50e-01 | 1.04e-01 | 0.89700 |
| Other semaphorin interactions | 18 | 4.46e-01 | 1.04e-01 | 0.94500 |
| Blood group systems biosynthesis | 12 | 5.35e-01 | -1.04e-01 | 0.94500 |
| Processing of SMDT1 | 11 | 5.52e-01 | 1.04e-01 | 0.94500 |
| Cholesterol biosynthesis | 16 | 4.75e-01 | -1.03e-01 | 0.94500 |
| Transcriptional regulation by small RNAs | 29 | 3.37e-01 | 1.03e-01 | 0.92900 |
| Inositol phosphate metabolism | 39 | 2.66e-01 | 1.03e-01 | 0.89800 |
| Signaling by NTRK1 (TRKA) | 99 | 7.71e-02 | 1.03e-01 | 0.85100 |
| Ion homeostasis | 41 | 2.56e-01 | 1.03e-01 | 0.89700 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 39 | 2.69e-01 | 1.02e-01 | 0.89800 |
| Sema4D induced cell migration and growth-cone collapse | 16 | 4.80e-01 | -1.02e-01 | 0.94500 |
| Common Pathway of Fibrin Clot Formation | 18 | 4.54e-01 | -1.02e-01 | 0.94500 |
| Inflammasomes | 16 | 4.81e-01 | 1.02e-01 | 0.94500 |
| Interleukin-27 signaling | 10 | 5.78e-01 | 1.02e-01 | 0.94500 |
| RNA Polymerase I Transcription | 34 | 3.05e-01 | -1.02e-01 | 0.92300 |
| Association of TriC/CCT with target proteins during biosynthesis | 30 | 3.37e-01 | 1.01e-01 | 0.92900 |
| SUMOylation of RNA binding proteins | 35 | 3.00e-01 | 1.01e-01 | 0.91700 |
| Nuclear Envelope Breakdown | 37 | 2.87e-01 | 1.01e-01 | 0.90700 |
| Signaling by TGF-beta Receptor Complex | 50 | 2.17e-01 | -1.01e-01 | 0.89700 |
| Cell-cell junction organization | 47 | 2.31e-01 | -1.01e-01 | 0.89700 |
| Signaling by NTRK2 (TRKB) | 21 | 4.24e-01 | 1.01e-01 | 0.94500 |
| Dectin-1 mediated noncanonical NF-kB signaling | 42 | 2.58e-01 | -1.01e-01 | 0.89700 |
| Toll Like Receptor 3 (TLR3) Cascade | 73 | 1.37e-01 | 1.01e-01 | 0.88500 |
| Cell junction organization | 69 | 1.50e-01 | -1.00e-01 | 0.88800 |
| Ub-specific processing proteases | 127 | 5.13e-02 | 1.00e-01 | 0.85100 |
| Mitotic G1 phase and G1/S transition | 106 | 7.49e-02 | 1.00e-01 | 0.85100 |
| Chaperonin-mediated protein folding | 71 | 1.45e-01 | 1.00e-01 | 0.88500 |
| Nucleotide salvage | 17 | 4.75e-01 | 1.00e-01 | 0.94500 |
| Transport of the SLBP independent Mature mRNA | 23 | 4.08e-01 | 9.96e-02 | 0.94500 |
| Purine ribonucleoside monophosphate biosynthesis | 11 | 5.68e-01 | 9.95e-02 | 0.94500 |
| PCP/CE pathway | 68 | 1.58e-01 | 9.90e-02 | 0.89700 |
| Regulation of gene expression by Hypoxia-inducible Factor | 11 | 5.70e-01 | 9.89e-02 | 0.94500 |
| Attenuation phase | 16 | 4.96e-01 | 9.84e-02 | 0.94500 |
| Nuclear Pore Complex (NPC) Disassembly | 25 | 3.97e-01 | 9.78e-02 | 0.94500 |
| Loss of Nlp from mitotic centrosomes | 55 | 2.13e-01 | 9.72e-02 | 0.89700 |
| Loss of proteins required for interphase microtubule organization from the centrosome | 55 | 2.13e-01 | 9.72e-02 | 0.89700 |
| Rap1 signalling | 14 | 5.29e-01 | 9.72e-02 | 0.94500 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 17 | 4.89e-01 | 9.70e-02 | 0.94500 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 26 | 3.92e-01 | -9.69e-02 | 0.94500 |
| Trafficking of AMPA receptors | 26 | 3.92e-01 | -9.69e-02 | 0.94500 |
| PKA activation in glucagon signalling | 15 | 5.16e-01 | 9.69e-02 | 0.94500 |
| FGFR2 mutant receptor activation | 20 | 4.54e-01 | -9.68e-02 | 0.94500 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 14 | 5.32e-01 | 9.66e-02 | 0.94500 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 14 | 5.32e-01 | 9.66e-02 | 0.94500 |
| Insulin receptor signalling cascade | 47 | 2.54e-01 | -9.62e-02 | 0.89700 |
| Cell Cycle, Mitotic | 364 | 1.74e-03 | 9.60e-02 | 0.35900 |
| Triglyceride metabolism | 28 | 3.80e-01 | -9.60e-02 | 0.94500 |
| Ca2+ pathway | 53 | 2.28e-01 | 9.58e-02 | 0.89700 |
| Transport of the SLBP Dependant Mature mRNA | 24 | 4.17e-01 | 9.57e-02 | 0.94500 |
| Growth hormone receptor signaling | 20 | 4.60e-01 | 9.56e-02 | 0.94500 |
| COPI-mediated anterograde transport | 67 | 1.77e-01 | -9.55e-02 | 0.89700 |
| Acetylcholine binding and downstream events | 12 | 5.67e-01 | -9.54e-02 | 0.94500 |
| Postsynaptic nicotinic acetylcholine receptors | 12 | 5.67e-01 | -9.54e-02 | 0.94500 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | 11 | 5.84e-01 | -9.53e-02 | 0.94500 |
| Selenoamino acid metabolism | 48 | 2.55e-01 | 9.49e-02 | 0.89700 |
| RNA Polymerase III Transcription Termination | 15 | 5.25e-01 | -9.49e-02 | 0.94500 |
| Signaling by NTRKs | 114 | 8.08e-02 | 9.48e-02 | 0.85100 |
| Hedgehog 'on' state | 57 | 2.16e-01 | -9.47e-02 | 0.89700 |
| Protein folding | 77 | 1.51e-01 | 9.47e-02 | 0.88800 |
| EGFR downregulation | 22 | 4.45e-01 | -9.42e-02 | 0.94500 |
| FCGR activation | 15 | 5.29e-01 | -9.39e-02 | 0.94500 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 91 | 1.22e-01 | -9.39e-02 | 0.88500 |
| Ovarian tumor domain proteases | 27 | 4.00e-01 | 9.37e-02 | 0.94500 |
| SUMOylation of chromatin organization proteins | 40 | 3.06e-01 | 9.36e-02 | 0.92300 |
| GABA synthesis, release, reuptake and degradation | 13 | 5.59e-01 | -9.36e-02 | 0.94500 |
| Signaling by high-kinase activity BRAF mutants | 27 | 4.01e-01 | 9.35e-02 | 0.94500 |
| Leading Strand Synthesis | 12 | 5.75e-01 | 9.34e-02 | 0.94500 |
| Polymerase switching | 12 | 5.75e-01 | 9.34e-02 | 0.94500 |
| Mitotic Prometaphase | 141 | 5.60e-02 | 9.34e-02 | 0.85100 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | 18 | 4.93e-01 | 9.33e-02 | 0.94500 |
| Signaling by TGFB family members | 76 | 1.60e-01 | -9.33e-02 | 0.89700 |
| Recycling of bile acids and salts | 13 | 5.60e-01 | 9.33e-02 | 0.94500 |
| APC-Cdc20 mediated degradation of Nek2A | 20 | 4.71e-01 | -9.31e-02 | 0.94500 |
| Signaling by ROBO receptors | 125 | 7.37e-02 | 9.28e-02 | 0.85100 |
| Intrinsic Pathway for Apoptosis | 42 | 3.00e-01 | 9.25e-02 | 0.91700 |
| Diseases associated with glycosylation precursor biosynthesis | 15 | 5.35e-01 | 9.25e-02 | 0.94500 |
| Regulation of PTEN gene transcription | 48 | 2.68e-01 | 9.24e-02 | 0.89800 |
| Activated point mutants of FGFR2 | 14 | 5.50e-01 | -9.22e-02 | 0.94500 |
| Keratan sulfate/keratin metabolism | 25 | 4.26e-01 | 9.20e-02 | 0.94500 |
| RAB GEFs exchange GTP for GDP on RABs | 67 | 1.97e-01 | 9.13e-02 | 0.89700 |
| cGMP effects | 16 | 5.28e-01 | -9.12e-02 | 0.94500 |
| Metabolism of fat-soluble vitamins | 31 | 3.80e-01 | -9.11e-02 | 0.94500 |
| RHO GTPases activate PAKs | 18 | 5.04e-01 | 9.10e-02 | 0.94500 |
| SUMOylation of DNA methylation proteins | 15 | 5.42e-01 | 9.09e-02 | 0.94500 |
| PPARA activates gene expression | 96 | 1.25e-01 | 9.08e-02 | 0.88500 |
| RA biosynthesis pathway | 18 | 5.05e-01 | 9.07e-02 | 0.94500 |
| Resolution of Abasic Sites (AP sites) | 30 | 3.91e-01 | 9.06e-02 | 0.94500 |
| Synthesis of PIPs at the early endosome membrane | 14 | 5.59e-01 | 9.02e-02 | 0.94500 |
| CS/DS degradation | 11 | 6.06e-01 | -8.99e-02 | 0.94700 |
| Long-term potentiation | 19 | 4.98e-01 | -8.98e-02 | 0.94500 |
| TP53 Regulates Metabolic Genes | 65 | 2.11e-01 | -8.97e-02 | 0.89700 |
| Retrograde neurotrophin signalling | 12 | 5.91e-01 | 8.96e-02 | 0.94500 |
| Nitric oxide stimulates guanylate cyclase | 21 | 4.78e-01 | -8.95e-02 | 0.94500 |
| Collagen biosynthesis and modifying enzymes | 54 | 2.57e-01 | -8.92e-02 | 0.89700 |
| Lagging Strand Synthesis | 16 | 5.37e-01 | 8.91e-02 | 0.94500 |
| IRE1alpha activates chaperones | 40 | 3.30e-01 | -8.90e-02 | 0.92900 |
| Degradation of cysteine and homocysteine | 11 | 6.09e-01 | 8.90e-02 | 0.94900 |
| Activation of BH3-only proteins | 27 | 4.24e-01 | 8.90e-02 | 0.94500 |
| Reduction of cytosolic Ca++ levels | 11 | 6.10e-01 | 8.89e-02 | 0.94900 |
| Uptake and actions of bacterial toxins | 27 | 4.25e-01 | -8.88e-02 | 0.94500 |
| p75 NTR receptor-mediated signalling | 78 | 1.76e-01 | -8.87e-02 | 0.89700 |
| RHO GTPase Effectors | 192 | 3.50e-02 | 8.85e-02 | 0.85100 |
| Telomere Maintenance | 43 | 3.16e-01 | 8.84e-02 | 0.92900 |
| Rab regulation of trafficking | 94 | 1.39e-01 | 8.84e-02 | 0.88500 |
| PKA activation | 15 | 5.55e-01 | 8.80e-02 | 0.94500 |
| CTLA4 inhibitory signaling | 19 | 5.07e-01 | -8.80e-02 | 0.94500 |
| Nonhomologous End-Joining (NHEJ) | 24 | 4.56e-01 | 8.79e-02 | 0.94500 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 27 | 4.30e-01 | 8.79e-02 | 0.94500 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 16 | 5.43e-01 | 8.78e-02 | 0.94500 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 33 | 3.83e-01 | 8.78e-02 | 0.94500 |
| NIK-->noncanonical NF-kB signaling | 39 | 3.44e-01 | -8.76e-02 | 0.92900 |
| Beta-catenin independent WNT signaling | 114 | 1.07e-01 | 8.75e-02 | 0.88500 |
| Negative regulation of TCF-dependent signaling by WNT ligand antagonists | 13 | 5.86e-01 | -8.73e-02 | 0.94500 |
| Potential therapeutics for SARS | 26 | 4.44e-01 | 8.68e-02 | 0.94500 |
| Factors involved in megakaryocyte development and platelet production | 99 | 1.36e-01 | 8.68e-02 | 0.88500 |
| Downregulation of TGF-beta receptor signaling | 17 | 5.36e-01 | -8.68e-02 | 0.94500 |
| Amino acid transport across the plasma membrane | 28 | 4.27e-01 | -8.68e-02 | 0.94500 |
| Signaling by FGFR3 in disease | 18 | 5.24e-01 | 8.67e-02 | 0.94500 |
| Signaling by FGFR3 point mutants in cancer | 18 | 5.24e-01 | 8.67e-02 | 0.94500 |
| Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon | 13 | 5.90e-01 | -8.63e-02 | 0.94500 |
| Signaling by KIT in disease | 17 | 5.38e-01 | 8.62e-02 | 0.94500 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 17 | 5.38e-01 | 8.62e-02 | 0.94500 |
| G beta:gamma signalling through BTK | 11 | 6.21e-01 | 8.61e-02 | 0.95500 |
| Gamma carboxylation, hypusine formation and arylsulfatase activation | 24 | 4.66e-01 | -8.61e-02 | 0.94500 |
| Signaling by EGFR | 38 | 3.59e-01 | -8.60e-02 | 0.93400 |
| Base-Excision Repair, AP Site Formation | 17 | 5.42e-01 | 8.54e-02 | 0.94500 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 24 | 4.69e-01 | 8.54e-02 | 0.94500 |
| Nuclear import of Rev protein | 23 | 4.80e-01 | 8.52e-02 | 0.94500 |
| Signaling by ERBB2 in Cancer | 21 | 5.00e-01 | 8.51e-02 | 0.94500 |
| M Phase | 263 | 1.79e-02 | 8.51e-02 | 0.80800 |
| CYP2E1 reactions | 10 | 6.41e-01 | 8.51e-02 | 0.95900 |
| LDL clearance | 16 | 5.58e-01 | 8.47e-02 | 0.94500 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | 16 | 5.58e-01 | -8.46e-02 | 0.94500 |
| Signaling by FGFR1 | 40 | 3.55e-01 | 8.45e-02 | 0.93100 |
| InlB-mediated entry of Listeria monocytogenes into host cell | 10 | 6.44e-01 | -8.44e-02 | 0.95900 |
| SHC1 events in EGFR signaling | 11 | 6.30e-01 | -8.40e-02 | 0.95500 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 69 | 2.28e-01 | 8.40e-02 | 0.89700 |
| Amplification of signal from the kinetochores | 69 | 2.28e-01 | 8.40e-02 | 0.89700 |
| Cellular response to heat stress | 68 | 2.32e-01 | 8.39e-02 | 0.89700 |
| Organic cation transport | 10 | 6.49e-01 | 8.31e-02 | 0.95900 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 30 | 4.33e-01 | 8.27e-02 | 0.94500 |
| Diseases of mitotic cell cycle | 30 | 4.33e-01 | 8.27e-02 | 0.94500 |
| Eukaryotic Translation Termination | 36 | 3.91e-01 | 8.26e-02 | 0.94500 |
| Plasma lipoprotein clearance | 29 | 4.44e-01 | 8.21e-02 | 0.94500 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 32 | 4.22e-01 | -8.21e-02 | 0.94500 |
| Interconversion of nucleotide di- and triphosphates | 22 | 5.06e-01 | 8.19e-02 | 0.94500 |
| Transcription of the HIV genome | 45 | 3.42e-01 | -8.19e-02 | 0.92900 |
| HDR through Homologous Recombination (HRR) | 43 | 3.53e-01 | -8.18e-02 | 0.93100 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 33 | 4.16e-01 | 8.18e-02 | 0.94500 |
| Phase 0 - rapid depolarisation | 37 | 3.90e-01 | -8.17e-02 | 0.94500 |
| Mitotic Metaphase and Anaphase | 173 | 6.44e-02 | 8.17e-02 | 0.85100 |
| IL-6-type cytokine receptor ligand interactions | 15 | 5.85e-01 | -8.16e-02 | 0.94500 |
| Processing of DNA double-strand break ends | 43 | 3.56e-01 | 8.13e-02 | 0.93100 |
| HATs acetylate histones | 58 | 2.84e-01 | 8.13e-02 | 0.90400 |
| PI-3K cascade:FGFR2 | 20 | 5.31e-01 | -8.09e-02 | 0.94500 |
| FGFR1 mutant receptor activation | 26 | 4.76e-01 | 8.08e-02 | 0.94500 |
| Costimulation by the CD28 family | 51 | 3.19e-01 | -8.07e-02 | 0.92900 |
| COPI-independent Golgi-to-ER retrograde traffic | 27 | 4.69e-01 | -8.05e-02 | 0.94500 |
| tRNA modification in the nucleus and cytosol | 28 | 4.62e-01 | 8.03e-02 | 0.94500 |
| Toll Like Receptor 9 (TLR9) Cascade | 71 | 2.43e-01 | 8.03e-02 | 0.89700 |
| Laminin interactions | 22 | 5.17e-01 | -7.98e-02 | 0.94500 |
| G alpha (z) signalling events | 36 | 4.09e-01 | 7.95e-02 | 0.94500 |
| Centrosome maturation | 65 | 2.70e-01 | 7.92e-02 | 0.89800 |
| Recruitment of mitotic centrosome proteins and complexes | 65 | 2.70e-01 | 7.92e-02 | 0.89800 |
| Recruitment of NuMA to mitotic centrosomes | 64 | 2.74e-01 | 7.91e-02 | 0.89800 |
| Cross-presentation of soluble exogenous antigens (endosomes) | 36 | 4.12e-01 | -7.90e-02 | 0.94500 |
| HCMV Late Events | 38 | 4.00e-01 | 7.90e-02 | 0.94500 |
| Dissolution of Fibrin Clot | 13 | 6.22e-01 | 7.90e-02 | 0.95500 |
| Meiotic recombination | 19 | 5.52e-01 | 7.87e-02 | 0.94500 |
| Platelet calcium homeostasis | 22 | 5.23e-01 | -7.87e-02 | 0.94500 |
| Mitotic Anaphase | 172 | 7.59e-02 | 7.86e-02 | 0.85100 |
| Cell Cycle | 456 | 4.37e-03 | 7.84e-02 | 0.58200 |
| HSF1 activation | 19 | 5.55e-01 | 7.82e-02 | 0.94500 |
| Glutathione conjugation | 29 | 4.66e-01 | -7.82e-02 | 0.94500 |
| TNFR1-induced NFkappaB signaling pathway | 22 | 5.27e-01 | -7.79e-02 | 0.94500 |
| Regulation of localization of FOXO transcription factors | 10 | 6.70e-01 | 7.78e-02 | 0.95900 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | 41 | 3.89e-01 | 7.77e-02 | 0.94500 |
| Regulation of TP53 Activity | 122 | 1.39e-01 | -7.77e-02 | 0.88500 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 50 | 3.44e-01 | -7.74e-02 | 0.92900 |
| Host Interactions of HIV factors | 92 | 2.00e-01 | 7.74e-02 | 0.89700 |
| MyD88 cascade initiated on plasma membrane | 63 | 2.89e-01 | 7.73e-02 | 0.90700 |
| Toll Like Receptor 10 (TLR10) Cascade | 63 | 2.89e-01 | 7.73e-02 | 0.90700 |
| Toll Like Receptor 5 (TLR5) Cascade | 63 | 2.89e-01 | 7.73e-02 | 0.90700 |
| GP1b-IX-V activation signalling | 10 | 6.74e-01 | 7.68e-02 | 0.95900 |
| Initial triggering of complement | 23 | 5.25e-01 | -7.66e-02 | 0.94500 |
| Processive synthesis on the C-strand of the telomere | 13 | 6.32e-01 | 7.66e-02 | 0.95700 |
| DAP12 signaling | 22 | 5.36e-01 | 7.63e-02 | 0.94500 |
| tRNA processing in the nucleus | 42 | 3.93e-01 | 7.62e-02 | 0.94500 |
| Tie2 Signaling | 16 | 5.98e-01 | -7.61e-02 | 0.94500 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 24 | 5.19e-01 | 7.61e-02 | 0.94500 |
| Unblocking of NMDA receptors, glutamate binding and activation | 17 | 5.89e-01 | -7.58e-02 | 0.94500 |
| STING mediated induction of host immune responses | 11 | 6.65e-01 | 7.54e-02 | 0.95900 |
| Sphingolipid metabolism | 63 | 3.03e-01 | 7.51e-02 | 0.91800 |
| NOTCH1 Intracellular Domain Regulates Transcription | 38 | 4.24e-01 | 7.49e-02 | 0.94500 |
| Erythropoietin activates RAS | 11 | 6.67e-01 | 7.49e-02 | 0.95900 |
| Apoptosis | 133 | 1.37e-01 | 7.48e-02 | 0.88500 |
| Processive synthesis on the lagging strand | 12 | 6.54e-01 | 7.47e-02 | 0.95900 |
| DAP12 interactions | 27 | 5.02e-01 | 7.47e-02 | 0.94500 |
| Glucuronidation | 16 | 6.05e-01 | 7.47e-02 | 0.94700 |
| RNA Polymerase III Transcription Initiation | 23 | 5.36e-01 | 7.46e-02 | 0.94500 |
| Programmed Cell Death | 136 | 1.34e-01 | 7.46e-02 | 0.88500 |
| ZBP1(DAI) mediated induction of type I IFNs | 19 | 5.75e-01 | -7.43e-02 | 0.94500 |
| Autodegradation of Cdh1 by Cdh1:APC/C | 46 | 3.85e-01 | -7.41e-02 | 0.94500 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 12 | 6.58e-01 | 7.38e-02 | 0.95900 |
| ERBB2 Regulates Cell Motility | 11 | 6.73e-01 | -7.35e-02 | 0.95900 |
| ER to Golgi Anterograde Transport | 106 | 1.92e-01 | -7.34e-02 | 0.89700 |
| FRS-mediated FGFR4 signaling | 17 | 6.01e-01 | -7.33e-02 | 0.94500 |
| Recognition of DNA damage by PCNA-containing replication complex | 19 | 5.81e-01 | 7.32e-02 | 0.94500 |
| TP53 Regulates Transcription of Cell Cycle Genes | 40 | 4.26e-01 | 7.28e-02 | 0.94500 |
| Fatty acid metabolism | 136 | 1.45e-01 | 7.24e-02 | 0.88500 |
| Regulation of lipid metabolism by PPARalpha | 98 | 2.17e-01 | 7.23e-02 | 0.89700 |
| Signaling by NOTCH2 | 24 | 5.40e-01 | -7.23e-02 | 0.94500 |
| RNA Pol II CTD phosphorylation and interaction with CE | 15 | 6.29e-01 | -7.20e-02 | 0.95500 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 15 | 6.29e-01 | -7.20e-02 | 0.95500 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 34 | 4.68e-01 | 7.19e-02 | 0.94500 |
| Signaling by RAS mutants | 34 | 4.68e-01 | 7.19e-02 | 0.94500 |
| Signaling by moderate kinase activity BRAF mutants | 34 | 4.68e-01 | 7.19e-02 | 0.94500 |
| Signaling downstream of RAS mutants | 34 | 4.68e-01 | 7.19e-02 | 0.94500 |
| FGFR2 alternative splicing | 14 | 6.41e-01 | 7.19e-02 | 0.95900 |
| G beta:gamma signalling through PI3Kgamma | 18 | 5.98e-01 | 7.18e-02 | 0.94500 |
| Signaling by FGFR4 in disease | 10 | 6.96e-01 | 7.15e-02 | 0.95900 |
| Signaling by SCF-KIT | 36 | 4.61e-01 | 7.11e-02 | 0.94500 |
| Protein localization | 114 | 1.91e-01 | -7.10e-02 | 0.89700 |
| Anchoring of the basal body to the plasma membrane | 76 | 2.85e-01 | 7.10e-02 | 0.90400 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 19 | 5.92e-01 | -7.10e-02 | 0.94500 |
| Formation of HIV elongation complex in the absence of HIV Tat | 23 | 5.57e-01 | -7.08e-02 | 0.94500 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 23 | 5.57e-01 | -7.08e-02 | 0.94500 |
| HIV Transcription Elongation | 23 | 5.57e-01 | -7.08e-02 | 0.94500 |
| Tat-mediated elongation of the HIV-1 transcript | 23 | 5.57e-01 | -7.08e-02 | 0.94500 |
| Presynaptic nicotinic acetylcholine receptors | 11 | 6.85e-01 | -7.07e-02 | 0.95900 |
| LGI-ADAM interactions | 13 | 6.60e-01 | -7.05e-02 | 0.95900 |
| RHO GTPases Activate Formins | 89 | 2.52e-01 | 7.04e-02 | 0.89700 |
| ER-Phagosome pathway | 55 | 3.68e-01 | -7.03e-02 | 0.94500 |
| SHC-mediated cascade:FGFR4 | 16 | 6.27e-01 | -7.01e-02 | 0.95500 |
| Regulation of TNFR1 signaling | 25 | 5.45e-01 | -7.00e-02 | 0.94500 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 31 | 5.02e-01 | 6.97e-02 | 0.94500 |
| SHC1 events in ERBB4 signaling | 10 | 7.03e-01 | -6.96e-02 | 0.95900 |
| Activation of the pre-replicative complex | 23 | 5.64e-01 | 6.96e-02 | 0.94500 |
| Interactions of Vpr with host cellular proteins | 25 | 5.49e-01 | 6.92e-02 | 0.94500 |
| RHO GTPases activate IQGAPs | 10 | 7.05e-01 | 6.92e-02 | 0.95900 |
| Metabolism of nucleotides | 78 | 2.92e-01 | 6.91e-02 | 0.90700 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 27 | 5.35e-01 | -6.91e-02 | 0.94500 |
| Diseases of metabolism | 193 | 9.94e-02 | -6.90e-02 | 0.87200 |
| Transport to the Golgi and subsequent modification | 129 | 1.78e-01 | -6.88e-02 | 0.89700 |
| Prostacyclin signalling through prostacyclin receptor | 13 | 6.70e-01 | 6.83e-02 | 0.95900 |
| Signaling by EGFR in Cancer | 18 | 6.16e-01 | -6.82e-02 | 0.95300 |
| RIP-mediated NFkB activation via ZBP1 | 15 | 6.48e-01 | -6.80e-02 | 0.95900 |
| Influenza Viral RNA Transcription and Replication | 62 | 3.60e-01 | 6.73e-02 | 0.93400 |
| Nucleotide Excision Repair | 76 | 3.11e-01 | 6.72e-02 | 0.92900 |
| Cellular hexose transport | 19 | 6.12e-01 | -6.72e-02 | 0.95000 |
| Regulation of FZD by ubiquitination | 14 | 6.64e-01 | 6.72e-02 | 0.95900 |
| Downstream signaling of activated FGFR4 | 22 | 5.86e-01 | -6.70e-02 | 0.94500 |
| Ethanol oxidation | 10 | 7.14e-01 | 6.69e-02 | 0.95900 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 20 | 6.06e-01 | 6.66e-02 | 0.94700 |
| Negative regulation of FGFR3 signaling | 21 | 5.98e-01 | 6.65e-02 | 0.94500 |
| Platelet homeostasis | 71 | 3.33e-01 | -6.65e-02 | 0.92900 |
| MyD88 dependent cascade initiated on endosome | 68 | 3.45e-01 | 6.63e-02 | 0.92900 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 68 | 3.45e-01 | 6.63e-02 | 0.92900 |
| Glycogen breakdown (glycogenolysis) | 12 | 6.91e-01 | 6.62e-02 | 0.95900 |
| Potassium Channels | 79 | 3.10e-01 | 6.62e-02 | 0.92800 |
| mRNA Splicing - Minor Pathway | 30 | 5.31e-01 | -6.61e-02 | 0.94500 |
| Diseases associated with glycosaminoglycan metabolism | 33 | 5.12e-01 | -6.59e-02 | 0.94500 |
| Downregulation of ERBB2 signaling | 19 | 6.19e-01 | -6.58e-02 | 0.95500 |
| EML4 and NUDC in mitotic spindle formation | 72 | 3.36e-01 | 6.57e-02 | 0.92900 |
| Regulation of RAS by GAPs | 50 | 4.24e-01 | 6.55e-02 | 0.94500 |
| Telomere C-strand synthesis initiation | 11 | 7.07e-01 | 6.55e-02 | 0.95900 |
| Regulation of HSF1-mediated heat shock response | 52 | 4.15e-01 | 6.54e-02 | 0.94500 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 11 | 7.10e-01 | 6.48e-02 | 0.95900 |
| Phospholipase C-mediated cascade; FGFR2 | 15 | 6.64e-01 | -6.48e-02 | 0.95900 |
| Regulation of beta-cell development | 29 | 5.47e-01 | 6.47e-02 | 0.94500 |
| Interleukin-20 family signaling | 20 | 6.17e-01 | -6.46e-02 | 0.95300 |
| FCGR3A-mediated phagocytosis | 55 | 4.08e-01 | 6.46e-02 | 0.94500 |
| Leishmania phagocytosis | 55 | 4.08e-01 | 6.46e-02 | 0.94500 |
| Parasite infection | 55 | 4.08e-01 | 6.46e-02 | 0.94500 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 45 | 4.55e-01 | 6.43e-02 | 0.94500 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 18 | 6.37e-01 | -6.43e-02 | 0.95900 |
| Fc epsilon receptor (FCERI) signaling | 98 | 2.73e-01 | 6.42e-02 | 0.89800 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 45 | 4.56e-01 | 6.42e-02 | 0.94500 |
| Major pathway of rRNA processing in the nucleolus and cytosol | 98 | 2.73e-01 | 6.41e-02 | 0.89800 |
| Influenza Infection | 75 | 3.40e-01 | 6.38e-02 | 0.92900 |
| E3 ubiquitin ligases ubiquitinate target proteins | 23 | 5.98e-01 | 6.35e-02 | 0.94500 |
| HIV Transcription Initiation | 32 | 5.37e-01 | -6.31e-02 | 0.94500 |
| RNA Polymerase II HIV Promoter Escape | 32 | 5.37e-01 | -6.31e-02 | 0.94500 |
| RNA Polymerase II Promoter Escape | 32 | 5.37e-01 | -6.31e-02 | 0.94500 |
| RNA Polymerase II Transcription Initiation | 32 | 5.37e-01 | -6.31e-02 | 0.94500 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 32 | 5.37e-01 | -6.31e-02 | 0.94500 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 32 | 5.37e-01 | -6.31e-02 | 0.94500 |
| MyD88-independent TLR4 cascade | 76 | 3.42e-01 | 6.31e-02 | 0.92900 |
| TRIF(TICAM1)-mediated TLR4 signaling | 76 | 3.42e-01 | 6.31e-02 | 0.92900 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 44 | 4.71e-01 | 6.29e-02 | 0.94500 |
| Miscellaneous transport and binding events | 16 | 6.63e-01 | -6.29e-02 | 0.95900 |
| Chromatin modifying enzymes | 151 | 1.83e-01 | 6.28e-02 | 0.89700 |
| Chromatin organization | 151 | 1.83e-01 | 6.28e-02 | 0.89700 |
| Collagen degradation | 33 | 5.33e-01 | -6.28e-02 | 0.94500 |
| Physiological factors | 10 | 7.31e-01 | -6.27e-02 | 0.95900 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 14 | 6.87e-01 | 6.23e-02 | 0.95900 |
| Pre-NOTCH Expression and Processing | 44 | 4.76e-01 | 6.21e-02 | 0.94500 |
| IKK complex recruitment mediated by RIP1 | 16 | 6.67e-01 | -6.21e-02 | 0.95900 |
| PTEN Regulation | 106 | 2.72e-01 | 6.18e-02 | 0.89800 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 16 | 6.71e-01 | 6.14e-02 | 0.95900 |
| Lysosome Vesicle Biogenesis | 26 | 5.88e-01 | 6.14e-02 | 0.94500 |
| SHC-mediated cascade:FGFR3 | 14 | 6.92e-01 | 6.12e-02 | 0.95900 |
| Chondroitin sulfate/dermatan sulfate metabolism | 42 | 4.93e-01 | 6.12e-02 | 0.94500 |
| Formation of Incision Complex in GG-NER | 29 | 5.69e-01 | 6.11e-02 | 0.94500 |
| SUMO E3 ligases SUMOylate target proteins | 123 | 2.45e-01 | 6.07e-02 | 0.89700 |
| PI Metabolism | 72 | 3.74e-01 | 6.06e-02 | 0.94500 |
| Metabolism of RNA | 440 | 3.04e-02 | 6.05e-02 | 0.85100 |
| CD28 co-stimulation | 29 | 5.73e-01 | -6.04e-02 | 0.94500 |
| Gap junction trafficking | 23 | 6.18e-01 | 6.02e-02 | 0.95300 |
| Caspase activation via extrinsic apoptotic signalling pathway | 21 | 6.34e-01 | -6.00e-02 | 0.95700 |
| Activation of NF-kappaB in B cells | 45 | 4.88e-01 | -5.98e-02 | 0.94500 |
| ERBB2 Activates PTK6 Signaling | 10 | 7.45e-01 | -5.94e-02 | 0.95900 |
| GRB2 events in ERBB2 signaling | 12 | 7.21e-01 | 5.94e-02 | 0.95900 |
| p130Cas linkage to MAPK signaling for integrins | 13 | 7.12e-01 | 5.92e-02 | 0.95900 |
| Interleukin-4 and Interleukin-13 signaling | 83 | 3.52e-01 | -5.92e-02 | 0.93100 |
| activated TAK1 mediates p38 MAPK activation | 14 | 7.02e-01 | -5.91e-02 | 0.95900 |
| VLDLR internalisation and degradation | 11 | 7.35e-01 | 5.90e-02 | 0.95900 |
| Signaling by Rho GTPases | 302 | 7.98e-02 | 5.88e-02 | 0.85100 |
| Triglyceride biosynthesis | 10 | 7.48e-01 | 5.87e-02 | 0.95900 |
| APC/C-mediated degradation of cell cycle proteins | 66 | 4.10e-01 | 5.87e-02 | 0.94500 |
| Regulation of mitotic cell cycle | 66 | 4.10e-01 | 5.87e-02 | 0.94500 |
| Formation of the beta-catenin:TCF transactivating complex | 29 | 5.86e-01 | -5.85e-02 | 0.94500 |
| rRNA processing | 111 | 2.91e-01 | 5.81e-02 | 0.90700 |
| Mitochondrial Fatty Acid Beta-Oxidation | 27 | 6.03e-01 | -5.78e-02 | 0.94700 |
| Inwardly rectifying K+ channels | 27 | 6.04e-01 | -5.77e-02 | 0.94700 |
| Interleukin-2 family signaling | 31 | 5.78e-01 | 5.77e-02 | 0.94500 |
| Post-translational protein phosphorylation | 80 | 3.73e-01 | -5.77e-02 | 0.94500 |
| MAP kinase activation | 49 | 4.86e-01 | 5.76e-02 | 0.94500 |
| trans-Golgi Network Vesicle Budding | 52 | 4.73e-01 | 5.76e-02 | 0.94500 |
| Pre-NOTCH Processing in Golgi | 14 | 7.10e-01 | -5.74e-02 | 0.95900 |
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 20 | 6.57e-01 | -5.74e-02 | 0.95900 |
| CDK-mediated phosphorylation and removal of Cdc6 | 53 | 4.71e-01 | -5.73e-02 | 0.94500 |
| Plasma lipoprotein assembly, remodeling, and clearance | 54 | 4.67e-01 | -5.73e-02 | 0.94500 |
| RUNX2 regulates bone development | 24 | 6.29e-01 | 5.71e-02 | 0.95500 |
| Signaling by FGFR3 | 30 | 5.89e-01 | 5.71e-02 | 0.94500 |
| Cyclin E associated events during G1/S transition | 58 | 4.53e-01 | 5.70e-02 | 0.94500 |
| Synthesis of IP2, IP, and Ins in the cytosol | 13 | 7.22e-01 | 5.69e-02 | 0.95900 |
| Extra-nuclear estrogen signaling | 62 | 4.39e-01 | -5.68e-02 | 0.94500 |
| Notch-HLH transcription pathway | 22 | 6.47e-01 | -5.65e-02 | 0.95900 |
| GABA receptor activation | 43 | 5.23e-01 | -5.64e-02 | 0.94500 |
| tRNA processing | 76 | 3.97e-01 | 5.63e-02 | 0.94500 |
| DNA strand elongation | 23 | 6.43e-01 | -5.58e-02 | 0.95900 |
| Epigenetic regulation of gene expression | 61 | 4.52e-01 | -5.58e-02 | 0.94500 |
| Neurotransmitter receptors and postsynaptic signal transmission | 146 | 2.47e-01 | -5.56e-02 | 0.89700 |
| Tryptophan catabolism | 12 | 7.39e-01 | 5.55e-02 | 0.95900 |
| Platelet degranulation | 102 | 3.34e-01 | 5.54e-02 | 0.92900 |
| MAPK6/MAPK4 signaling | 64 | 4.47e-01 | 5.51e-02 | 0.94500 |
| Detoxification of Reactive Oxygen Species | 24 | 6.41e-01 | 5.50e-02 | 0.95900 |
| Mitochondrial translation initiation | 56 | 4.78e-01 | 5.49e-02 | 0.94500 |
| FCGR3A-mediated IL10 synthesis | 37 | 5.64e-01 | 5.49e-02 | 0.94500 |
| Cell-Cell communication | 98 | 3.50e-01 | -5.48e-02 | 0.93100 |
| G2/M DNA damage checkpoint | 43 | 5.35e-01 | 5.47e-02 | 0.94500 |
| Signaling by ERBB2 | 37 | 5.65e-01 | -5.47e-02 | 0.94500 |
| Adenylate cyclase inhibitory pathway | 13 | 7.33e-01 | -5.46e-02 | 0.95900 |
| Transmission across Chemical Synapses | 193 | 1.93e-01 | -5.45e-02 | 0.89700 |
| Interleukin-15 signaling | 11 | 7.55e-01 | 5.44e-02 | 0.96000 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 23 | 6.53e-01 | -5.42e-02 | 0.95900 |
| Cytokine Signaling in Immune system | 622 | 2.24e-02 | 5.41e-02 | 0.80800 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 40 | 5.54e-01 | 5.41e-02 | 0.94500 |
| Misspliced GSK3beta mutants stabilize beta-catenin | 13 | 7.37e-01 | -5.38e-02 | 0.95900 |
| S33 mutants of beta-catenin aren't phosphorylated | 13 | 7.37e-01 | -5.38e-02 | 0.95900 |
| S37 mutants of beta-catenin aren't phosphorylated | 13 | 7.37e-01 | -5.38e-02 | 0.95900 |
| S45 mutants of beta-catenin aren't phosphorylated | 13 | 7.37e-01 | -5.38e-02 | 0.95900 |
| T41 mutants of beta-catenin aren't phosphorylated | 13 | 7.37e-01 | -5.38e-02 | 0.95900 |
| phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex | 13 | 7.37e-01 | -5.38e-02 | 0.95900 |
| Nicotinate metabolism | 21 | 6.71e-01 | -5.36e-02 | 0.95900 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 67 | 4.49e-01 | 5.36e-02 | 0.94500 |
| Processing of Capped Intron-Containing Pre-mRNA | 164 | 2.39e-01 | 5.34e-02 | 0.89700 |
| ADP signalling through P2Y purinoceptor 1 | 19 | 6.88e-01 | 5.32e-02 | 0.95900 |
| Molecules associated with elastic fibres | 28 | 6.27e-01 | -5.31e-02 | 0.95500 |
| Cellular response to hypoxia | 53 | 5.04e-01 | 5.31e-02 | 0.94500 |
| Beta-catenin phosphorylation cascade | 15 | 7.23e-01 | 5.30e-02 | 0.95900 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | 16 | 7.15e-01 | 5.28e-02 | 0.95900 |
| Signaling by ERBB4 | 43 | 5.50e-01 | -5.27e-02 | 0.94500 |
| S Phase | 120 | 3.21e-01 | 5.25e-02 | 0.92900 |
| SUMOylation | 128 | 3.10e-01 | 5.21e-02 | 0.92800 |
| ABC transporters in lipid homeostasis | 13 | 7.46e-01 | 5.19e-02 | 0.95900 |
| TNFR1-induced proapoptotic signaling | 12 | 7.57e-01 | 5.17e-02 | 0.96000 |
| RMTs methylate histone arginines | 26 | 6.49e-01 | 5.16e-02 | 0.95900 |
| Diseases of carbohydrate metabolism | 25 | 6.58e-01 | 5.12e-02 | 0.95900 |
| FGFR2 ligand binding and activation | 16 | 7.23e-01 | -5.11e-02 | 0.95900 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 22 | 6.80e-01 | 5.08e-02 | 0.95900 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 22 | 6.80e-01 | 5.08e-02 | 0.95900 |
| Biological oxidations | 167 | 2.61e-01 | 5.05e-02 | 0.89800 |
| ROS and RNS production in phagocytes | 26 | 6.56e-01 | 5.05e-02 | 0.95900 |
| Autodegradation of the E3 ubiquitin ligase COP1 | 36 | 6.01e-01 | -5.04e-02 | 0.94500 |
| Dual incision in TC-NER | 44 | 5.64e-01 | 5.02e-02 | 0.94500 |
| Activation of ATR in response to replication stress | 23 | 6.77e-01 | 5.02e-02 | 0.95900 |
| DNA Double Strand Break Response | 34 | 6.14e-01 | 5.00e-02 | 0.95100 |
| Cellular responses to stress | 338 | 1.16e-01 | 4.99e-02 | 0.88500 |
| Class A/1 (Rhodopsin-like receptors) | 252 | 1.76e-01 | -4.97e-02 | 0.89700 |
| Keratinization | 94 | 4.06e-01 | -4.96e-02 | 0.94500 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 32 | 6.27e-01 | -4.96e-02 | 0.95500 |
| RAF activation | 28 | 6.50e-01 | 4.96e-02 | 0.95900 |
| rRNA processing in the nucleus and cytosol | 104 | 3.84e-01 | 4.95e-02 | 0.94500 |
| Trafficking of GluR2-containing AMPA receptors | 13 | 7.58e-01 | 4.95e-02 | 0.96000 |
| Acyl chain remodelling of PG | 15 | 7.42e-01 | -4.90e-02 | 0.95900 |
| Phospholipase C-mediated cascade; FGFR3 | 10 | 7.89e-01 | 4.90e-02 | 0.96400 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 68 | 4.87e-01 | 4.88e-02 | 0.94500 |
| Signaling by ERBB2 TMD/JMD mutants | 17 | 7.28e-01 | 4.88e-02 | 0.95900 |
| FRS-mediated FGFR3 signaling | 15 | 7.44e-01 | 4.88e-02 | 0.95900 |
| Synthesis of bile acids and bile salts | 25 | 6.74e-01 | -4.86e-02 | 0.95900 |
| Negative regulators of DDX58/IFIH1 signaling | 22 | 6.94e-01 | -4.85e-02 | 0.95900 |
| TAK1 activates NFkB by phosphorylation and activation of IKKs complex | 20 | 7.09e-01 | -4.83e-02 | 0.95900 |
| Transport of inorganic cations/anions and amino acids/oligopeptides | 90 | 4.29e-01 | -4.83e-02 | 0.94500 |
| Olfactory Signaling Pathway | 146 | 3.16e-01 | -4.82e-02 | 0.92900 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 13 | 7.64e-01 | 4.81e-02 | 0.96100 |
| Estrogen-dependent gene expression | 72 | 4.81e-01 | 4.80e-02 | 0.94500 |
| Cyclin A:Cdk2-associated events at S phase entry | 60 | 5.21e-01 | 4.79e-02 | 0.94500 |
| Phosphorylation of CD3 and TCR zeta chains | 14 | 7.56e-01 | -4.79e-02 | 0.96000 |
| Pre-NOTCH Transcription and Translation | 31 | 6.45e-01 | 4.79e-02 | 0.95900 |
| G alpha (s) signalling events | 261 | 1.85e-01 | -4.79e-02 | 0.89700 |
| Cell Cycle Checkpoints | 186 | 2.62e-01 | 4.79e-02 | 0.89800 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | 142 | 3.26e-01 | -4.79e-02 | 0.92900 |
| APC/C:Cdc20 mediated degradation of Securin | 50 | 5.59e-01 | -4.78e-02 | 0.94500 |
| Metabolism of folate and pterines | 14 | 7.59e-01 | -4.74e-02 | 0.96000 |
| SLC-mediated transmembrane transport | 206 | 2.42e-01 | 4.74e-02 | 0.89700 |
| Mitotic Spindle Checkpoint | 84 | 4.53e-01 | 4.74e-02 | 0.94500 |
| Signaling by Leptin | 10 | 7.96e-01 | 4.73e-02 | 0.96400 |
| Homology Directed Repair | 72 | 4.88e-01 | 4.73e-02 | 0.94500 |
| Metabolism of carbohydrates | 222 | 2.26e-01 | -4.73e-02 | 0.89700 |
| Mitophagy | 18 | 7.29e-01 | 4.72e-02 | 0.95900 |
| Death Receptor Signalling | 113 | 3.87e-01 | -4.72e-02 | 0.94500 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 18 | 7.29e-01 | -4.72e-02 | 0.95900 |
| Ca-dependent events | 30 | 6.55e-01 | 4.71e-02 | 0.95900 |
| Bile acid and bile salt metabolism | 32 | 6.45e-01 | 4.71e-02 | 0.95900 |
| Collagen chain trimerization | 39 | 6.12e-01 | -4.69e-02 | 0.95000 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 15 | 7.54e-01 | 4.68e-02 | 0.96000 |
| DNA Repair | 200 | 2.55e-01 | 4.68e-02 | 0.89700 |
| Signal amplification | 24 | 6.92e-01 | -4.68e-02 | 0.95900 |
| FOXO-mediated transcription of cell cycle genes | 14 | 7.62e-01 | -4.67e-02 | 0.96100 |
| Regulation of IFNG signaling | 10 | 8.00e-01 | -4.63e-02 | 0.96600 |
| PI-3K cascade:FGFR1 | 19 | 7.27e-01 | -4.63e-02 | 0.95900 |
| Signaling by ERBB2 KD Mutants | 20 | 7.22e-01 | 4.60e-02 | 0.95900 |
| Repression of WNT target genes | 11 | 7.92e-01 | 4.60e-02 | 0.96400 |
| Visual phototransduction | 74 | 4.98e-01 | -4.56e-02 | 0.94500 |
| Cellular responses to external stimuli | 345 | 1.47e-01 | 4.56e-02 | 0.88800 |
| Synthesis of PE | 10 | 8.03e-01 | 4.55e-02 | 0.96700 |
| Digestion | 16 | 7.54e-01 | -4.53e-02 | 0.96000 |
| Cytosolic sulfonation of small molecules | 17 | 7.47e-01 | -4.52e-02 | 0.95900 |
| Branched-chain amino acid catabolism | 19 | 7.33e-01 | 4.52e-02 | 0.95900 |
| EPH-ephrin mediated repulsion of cells | 39 | 6.26e-01 | -4.51e-02 | 0.95500 |
| Cytosolic sensors of pathogen-associated DNA | 46 | 5.98e-01 | 4.50e-02 | 0.94500 |
| Creatine metabolism | 10 | 8.06e-01 | 4.50e-02 | 0.96700 |
| PD-1 signaling | 13 | 7.79e-01 | -4.49e-02 | 0.96200 |
| Fanconi Anemia Pathway | 23 | 7.09e-01 | -4.49e-02 | 0.95900 |
| BBSome-mediated cargo-targeting to cilium | 18 | 7.42e-01 | 4.49e-02 | 0.95900 |
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 66 | 5.29e-01 | -4.49e-02 | 0.94500 |
| Global Genome Nucleotide Excision Repair (GG-NER) | 61 | 5.45e-01 | 4.48e-02 | 0.94500 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 46 | 6.00e-01 | 4.47e-02 | 0.94500 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 46 | 6.00e-01 | 4.47e-02 | 0.94500 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 46 | 6.00e-01 | 4.47e-02 | 0.94500 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 46 | 6.00e-01 | 4.47e-02 | 0.94500 |
| Signaling by NOTCH1 in Cancer | 46 | 6.00e-01 | 4.47e-02 | 0.94500 |
| Chemokine receptors bind chemokines | 38 | 6.35e-01 | -4.46e-02 | 0.95700 |
| mRNA Capping | 16 | 7.58e-01 | -4.44e-02 | 0.96000 |
| Thrombin signalling through proteinase activated receptors (PARs) | 24 | 7.07e-01 | -4.44e-02 | 0.95900 |
| TBC/RABGAPs | 33 | 6.61e-01 | 4.41e-02 | 0.95900 |
| Stabilization of p53 | 39 | 6.34e-01 | -4.40e-02 | 0.95700 |
| Late Phase of HIV Life Cycle | 87 | 4.79e-01 | -4.39e-02 | 0.94500 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 64 | 5.45e-01 | -4.38e-02 | 0.94500 |
| Gap junction assembly | 15 | 7.70e-01 | -4.36e-02 | 0.96200 |
| NOTCH3 Intracellular Domain Regulates Transcription | 22 | 7.24e-01 | 4.35e-02 | 0.95900 |
| Gap junction trafficking and regulation | 25 | 7.07e-01 | 4.35e-02 | 0.95900 |
| DNA Replication Pre-Initiation | 59 | 5.64e-01 | 4.35e-02 | 0.94500 |
| Signaling by FGFR2 | 50 | 5.96e-01 | 4.34e-02 | 0.94500 |
| Inhibition of DNA recombination at telomere | 12 | 7.95e-01 | 4.33e-02 | 0.96400 |
| Viral Messenger RNA Synthesis | 25 | 7.09e-01 | 4.32e-02 | 0.95900 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 15 | 7.73e-01 | -4.31e-02 | 0.96200 |
| Degradation of AXIN | 37 | 6.50e-01 | -4.31e-02 | 0.95900 |
| Semaphorin interactions | 54 | 5.85e-01 | -4.30e-02 | 0.94500 |
| Gene Silencing by RNA | 52 | 5.92e-01 | 4.29e-02 | 0.94500 |
| EPH-Ephrin signaling | 73 | 5.27e-01 | -4.29e-02 | 0.94500 |
| GPCR downstream signalling | 694 | 5.71e-02 | -4.28e-02 | 0.85100 |
| RET signaling | 36 | 6.58e-01 | -4.26e-02 | 0.95900 |
| FGFR1 ligand binding and activation | 13 | 7.91e-01 | -4.25e-02 | 0.96400 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | 12 | 8.00e-01 | 4.24e-02 | 0.96600 |
| UCH proteinases | 61 | 5.68e-01 | 4.23e-02 | 0.94500 |
| Mitochondrial biogenesis | 61 | 5.71e-01 | 4.20e-02 | 0.94500 |
| Signaling by GPCR | 740 | 5.49e-02 | -4.19e-02 | 0.85100 |
| G2/M Checkpoints | 91 | 4.91e-01 | 4.19e-02 | 0.94500 |
| Oncogenic MAPK signaling | 61 | 5.72e-01 | 4.18e-02 | 0.94500 |
| Chromosome Maintenance | 57 | 5.85e-01 | 4.18e-02 | 0.94500 |
| Separation of Sister Chromatids | 126 | 4.19e-01 | 4.18e-02 | 0.94500 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 54 | 5.96e-01 | 4.18e-02 | 0.94500 |
| HCMV Infection | 60 | 5.76e-01 | 4.17e-02 | 0.94500 |
| Stimuli-sensing channels | 78 | 5.24e-01 | -4.17e-02 | 0.94500 |
| Signaling by VEGF | 91 | 4.92e-01 | -4.17e-02 | 0.94500 |
| Adrenaline,noradrenaline inhibits insulin secretion | 22 | 7.35e-01 | 4.17e-02 | 0.95900 |
| MTOR signalling | 31 | 6.89e-01 | 4.16e-02 | 0.95900 |
| Signaling by Interleukins | 323 | 2.02e-01 | 4.15e-02 | 0.89700 |
| Transcriptional regulation of pluripotent stem cells | 22 | 7.36e-01 | -4.15e-02 | 0.95900 |
| Cleavage of the damaged pyrimidine | 15 | 7.81e-01 | 4.14e-02 | 0.96200 |
| Depyrimidination | 15 | 7.81e-01 | 4.14e-02 | 0.96200 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 15 | 7.81e-01 | 4.14e-02 | 0.96200 |
| FOXO-mediated transcription | 55 | 5.96e-01 | 4.14e-02 | 0.94500 |
| NR1H2 and NR1H3-mediated signaling | 40 | 6.53e-01 | 4.10e-02 | 0.95900 |
| G-protein activation | 20 | 7.52e-01 | -4.08e-02 | 0.96000 |
| Asparagine N-linked glycosylation | 218 | 3.02e-01 | -4.07e-02 | 0.91800 |
| Apoptotic factor-mediated response | 11 | 8.16e-01 | 4.06e-02 | 0.96700 |
| Presynaptic depolarization and calcium channel opening | 11 | 8.16e-01 | -4.05e-02 | 0.96700 |
| VEGFA-VEGFR2 Pathway | 85 | 5.21e-01 | -4.04e-02 | 0.94500 |
| Respiratory electron transport | 60 | 5.90e-01 | -4.02e-02 | 0.94500 |
| Scavenging by Class A Receptors | 14 | 7.94e-01 | 4.02e-02 | 0.96400 |
| Neuronal System | 306 | 2.30e-01 | -4.01e-02 | 0.89700 |
| Reproduction | 65 | 5.77e-01 | 4.00e-02 | 0.94500 |
| Glycogen metabolism | 21 | 7.52e-01 | -3.98e-02 | 0.96000 |
| MET promotes cell motility | 26 | 7.26e-01 | 3.98e-02 | 0.95900 |
| HSF1-dependent transactivation | 25 | 7.32e-01 | 3.95e-02 | 0.95900 |
| Senescence-Associated Secretory Phenotype (SASP) | 39 | 6.70e-01 | -3.95e-02 | 0.95900 |
| Metal ion SLC transporters | 19 | 7.66e-01 | -3.95e-02 | 0.96200 |
| Phospholipid metabolism | 163 | 3.87e-01 | 3.94e-02 | 0.94500 |
| Translation | 156 | 4.01e-01 | 3.91e-02 | 0.94500 |
| VEGFR2 mediated cell proliferation | 19 | 7.70e-01 | 3.88e-02 | 0.96200 |
| Peroxisomal lipid metabolism | 23 | 7.48e-01 | -3.87e-02 | 0.95900 |
| Interleukin-37 signaling | 15 | 7.95e-01 | 3.87e-02 | 0.96400 |
| Metabolism of Angiotensinogen to Angiotensins | 13 | 8.09e-01 | 3.86e-02 | 0.96700 |
| TCR signaling | 83 | 5.44e-01 | 3.86e-02 | 0.94500 |
| Regulation of APC/C activators between G1/S and early anaphase | 59 | 6.08e-01 | 3.86e-02 | 0.94900 |
| Downstream signaling of activated FGFR2 | 25 | 7.40e-01 | -3.83e-02 | 0.95900 |
| Formation of RNA Pol II elongation complex | 33 | 7.04e-01 | 3.82e-02 | 0.95900 |
| RNA Polymerase II Transcription Elongation | 33 | 7.04e-01 | 3.82e-02 | 0.95900 |
| Defects in vitamin and cofactor metabolism | 15 | 7.99e-01 | 3.81e-02 | 0.96600 |
| Mitochondrial translation elongation | 56 | 6.23e-01 | 3.80e-02 | 0.95500 |
| NS1 Mediated Effects on Host Pathways | 26 | 7.38e-01 | 3.79e-02 | 0.95900 |
| Telomere C-strand (Lagging Strand) Synthesis | 25 | 7.43e-01 | 3.79e-02 | 0.95900 |
| Integration of energy metabolism | 94 | 5.27e-01 | 3.78e-02 | 0.94500 |
| Downstream signaling events of B Cell Receptor (BCR) | 57 | 6.23e-01 | -3.77e-02 | 0.95500 |
| Nicotinamide salvaging | 11 | 8.29e-01 | -3.76e-02 | 0.96800 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 71 | 5.85e-01 | 3.76e-02 | 0.94500 |
| Toll Like Receptor 2 (TLR2) Cascade | 71 | 5.85e-01 | 3.76e-02 | 0.94500 |
| Toll Like Receptor TLR1:TLR2 Cascade | 71 | 5.85e-01 | 3.76e-02 | 0.94500 |
| Toll Like Receptor TLR6:TLR2 Cascade | 71 | 5.85e-01 | 3.76e-02 | 0.94500 |
| HDACs deacetylate histones | 22 | 7.61e-01 | 3.75e-02 | 0.96000 |
| Interleukin-1 signaling | 73 | 5.81e-01 | 3.74e-02 | 0.94500 |
| Dual Incision in GG-NER | 32 | 7.15e-01 | 3.74e-02 | 0.95900 |
| Orc1 removal from chromatin | 49 | 6.52e-01 | 3.72e-02 | 0.95900 |
| Response to elevated platelet cytosolic Ca2+ | 106 | 5.09e-01 | 3.72e-02 | 0.94500 |
| Diseases associated with N-glycosylation of proteins | 14 | 8.10e-01 | -3.71e-02 | 0.96700 |
| Cell death signalling via NRAGE, NRIF and NADE | 62 | 6.14e-01 | -3.71e-02 | 0.95100 |
| mRNA Splicing - Major Pathway | 118 | 4.90e-01 | 3.68e-02 | 0.94500 |
| NRAGE signals death through JNK | 53 | 6.43e-01 | -3.68e-02 | 0.95900 |
| Transcriptional Regulation by TP53 | 261 | 3.09e-01 | -3.67e-02 | 0.92800 |
| COPII-mediated vesicle transport | 51 | 6.52e-01 | 3.65e-02 | 0.95900 |
| Signaling by PDGF | 47 | 6.65e-01 | -3.65e-02 | 0.95900 |
| FRS-mediated FGFR2 signaling | 20 | 7.77e-01 | -3.65e-02 | 0.96200 |
| Signaling by Retinoic Acid | 38 | 6.97e-01 | -3.65e-02 | 0.95900 |
| CLEC7A (Dectin-1) signaling | 71 | 5.98e-01 | -3.62e-02 | 0.94500 |
| Zinc transporters | 12 | 8.29e-01 | -3.59e-02 | 0.96800 |
| Translesion synthesis by POLI | 12 | 8.30e-01 | -3.58e-02 | 0.96800 |
| Translesion synthesis by REV1 | 11 | 8.38e-01 | -3.57e-02 | 0.96800 |
| TNF signaling | 32 | 7.27e-01 | -3.57e-02 | 0.95900 |
| Activation of NMDA receptors and postsynaptic events | 63 | 6.25e-01 | -3.56e-02 | 0.95500 |
| Presynaptic function of Kainate receptors | 15 | 8.11e-01 | 3.56e-02 | 0.96700 |
| Interleukin-1 family signaling | 99 | 5.46e-01 | 3.51e-02 | 0.94500 |
| Termination of translesion DNA synthesis | 22 | 7.76e-01 | 3.51e-02 | 0.96200 |
| G-protein mediated events | 46 | 6.82e-01 | -3.49e-02 | 0.95900 |
| DNA Damage Recognition in GG-NER | 26 | 7.58e-01 | -3.49e-02 | 0.96000 |
| Glucose metabolism | 72 | 6.10e-01 | -3.48e-02 | 0.94900 |
| The citric acid (TCA) cycle and respiratory electron transport | 103 | 5.47e-01 | -3.44e-02 | 0.94500 |
| DCC mediated attractive signaling | 12 | 8.37e-01 | 3.44e-02 | 0.96800 |
| G beta:gamma signalling through PLC beta | 14 | 8.24e-01 | 3.43e-02 | 0.96800 |
| PINK1-PRKN Mediated Mitophagy | 14 | 8.25e-01 | -3.41e-02 | 0.96800 |
| Signaling by MET | 55 | 6.63e-01 | -3.40e-02 | 0.95900 |
| Interleukin-17 signaling | 55 | 6.66e-01 | 3.37e-02 | 0.95900 |
| SCF(Skp2)-mediated degradation of p27/p21 | 41 | 7.10e-01 | 3.36e-02 | 0.95900 |
| Hh mutants abrogate ligand secretion | 39 | 7.16e-01 | -3.36e-02 | 0.95900 |
| AMER1 mutants destabilize the destruction complex | 12 | 8.41e-01 | -3.34e-02 | 0.96800 |
| APC truncation mutants have impaired AXIN binding | 12 | 8.41e-01 | -3.34e-02 | 0.96800 |
| AXIN missense mutants destabilize the destruction complex | 12 | 8.41e-01 | -3.34e-02 | 0.96800 |
| AXIN mutants destabilize the destruction complex, activating WNT signaling | 12 | 8.41e-01 | -3.34e-02 | 0.96800 |
| Truncations of AMER1 destabilize the destruction complex | 12 | 8.41e-01 | -3.34e-02 | 0.96800 |
| truncated APC mutants destabilize the destruction complex | 12 | 8.41e-01 | -3.34e-02 | 0.96800 |
| Unfolded Protein Response (UPR) | 67 | 6.40e-01 | -3.31e-02 | 0.95900 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 88 | 5.97e-01 | -3.26e-02 | 0.94500 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 24 | 7.83e-01 | 3.26e-02 | 0.96200 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 27 | 7.71e-01 | 3.24e-02 | 0.96200 |
| Neddylation | 171 | 4.67e-01 | -3.23e-02 | 0.94500 |
| Assembly and cell surface presentation of NMDA receptors | 21 | 8.00e-01 | -3.19e-02 | 0.96600 |
| Regulation of actin dynamics for phagocytic cup formation | 56 | 6.80e-01 | 3.19e-02 | 0.95900 |
| SHC-mediated cascade:FGFR2 | 19 | 8.10e-01 | -3.19e-02 | 0.96700 |
| Neutrophil degranulation | 339 | 3.17e-01 | -3.18e-02 | 0.92900 |
| NCAM signaling for neurite out-growth | 48 | 7.05e-01 | -3.16e-02 | 0.95900 |
| Cardiac conduction | 114 | 5.66e-01 | 3.12e-02 | 0.94500 |
| DAG and IP3 signaling | 34 | 7.53e-01 | 3.12e-02 | 0.96000 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 37 | 7.47e-01 | -3.07e-02 | 0.95900 |
| Polymerase switching on the C-strand of the telomere | 21 | 8.08e-01 | 3.06e-02 | 0.96700 |
| Oxidative Stress Induced Senescence | 53 | 7.00e-01 | -3.06e-02 | 0.95900 |
| Hedgehog 'off' state | 74 | 6.53e-01 | 3.03e-02 | 0.95900 |
| Interaction between L1 and Ankyrins | 27 | 7.86e-01 | 3.02e-02 | 0.96300 |
| Signaling by FGFR | 62 | 6.82e-01 | 3.01e-02 | 0.95900 |
| Ephrin signaling | 17 | 8.30e-01 | 3.01e-02 | 0.96800 |
| Infection with Mycobacterium tuberculosis | 22 | 8.09e-01 | 2.97e-02 | 0.96700 |
| Cargo recognition for clathrin-mediated endocytosis | 76 | 6.56e-01 | -2.96e-02 | 0.95900 |
| Post NMDA receptor activation events | 53 | 7.10e-01 | -2.96e-02 | 0.95900 |
| Metabolism of vitamins and cofactors | 138 | 5.50e-01 | -2.95e-02 | 0.94500 |
| CRMPs in Sema3A signaling | 14 | 8.48e-01 | -2.95e-02 | 0.97200 |
| Classical antibody-mediated complement activation | 10 | 8.72e-01 | -2.94e-02 | 0.97800 |
| Degradation of beta-catenin by the destruction complex | 62 | 6.90e-01 | 2.93e-02 | 0.95900 |
| ABC transporter disorders | 53 | 7.12e-01 | -2.93e-02 | 0.95900 |
| TICAM1, RIP1-mediated IKK complex recruitment | 13 | 8.55e-01 | 2.92e-02 | 0.97400 |
| GRB2 events in EGFR signaling | 10 | 8.75e-01 | -2.88e-02 | 0.97800 |
| rRNA modification in the nucleus and cytosol | 43 | 7.46e-01 | -2.86e-02 | 0.95900 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | 61 | 7.00e-01 | 2.85e-02 | 0.95900 |
| Amine ligand-binding receptors | 34 | 7.74e-01 | -2.85e-02 | 0.96200 |
| Voltage gated Potassium channels | 31 | 7.84e-01 | -2.84e-02 | 0.96300 |
| Muscle contraction | 170 | 5.24e-01 | 2.84e-02 | 0.94500 |
| Complex I biogenesis | 35 | 7.73e-01 | 2.82e-02 | 0.96200 |
| SHC1 events in ERBB2 signaling | 18 | 8.37e-01 | 2.81e-02 | 0.96800 |
| Opioid Signalling | 73 | 6.80e-01 | 2.80e-02 | 0.95900 |
| Regulation of ornithine decarboxylase (ODC) | 36 | 7.73e-01 | 2.78e-02 | 0.96200 |
| Neurotransmitter release cycle | 36 | 7.74e-01 | -2.77e-02 | 0.96200 |
| Peptide hormone metabolism | 63 | 7.04e-01 | 2.77e-02 | 0.95900 |
| AKT phosphorylates targets in the cytosol | 13 | 8.63e-01 | -2.76e-02 | 0.97700 |
| ADP signalling through P2Y purinoceptor 12 | 15 | 8.53e-01 | -2.76e-02 | 0.97400 |
| Signaling by Hedgehog | 100 | 6.35e-01 | -2.75e-02 | 0.95700 |
| RNA Polymerase II Transcription | 822 | 1.85e-01 | 2.75e-02 | 0.89700 |
| Activation of G protein gated Potassium channels | 21 | 8.27e-01 | 2.75e-02 | 0.96800 |
| G protein gated Potassium channels | 21 | 8.27e-01 | 2.75e-02 | 0.96800 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 21 | 8.27e-01 | 2.75e-02 | 0.96800 |
| RNA polymerase II transcribes snRNA genes | 46 | 7.47e-01 | -2.75e-02 | 0.95900 |
| Signaling by BRAF and RAF fusions | 49 | 7.40e-01 | 2.74e-02 | 0.95900 |
| Nucleobase biosynthesis | 13 | 8.65e-01 | 2.73e-02 | 0.97700 |
| Antigen processing: Ubiquitination & Proteasome degradation | 232 | 4.77e-01 | 2.72e-02 | 0.94500 |
| Gene expression (Transcription) | 920 | 1.68e-01 | 2.71e-02 | 0.89700 |
| Mitochondrial translation termination | 56 | 7.26e-01 | 2.71e-02 | 0.95900 |
| Activation of the phototransduction cascade | 11 | 8.77e-01 | -2.69e-02 | 0.97900 |
| Negative regulation of FGFR1 signaling | 25 | 8.16e-01 | 2.69e-02 | 0.96700 |
| Retrograde transport at the Trans-Golgi-Network | 37 | 7.78e-01 | -2.68e-02 | 0.96200 |
| FGFR3 ligand binding and activation | 10 | 8.85e-01 | -2.65e-02 | 0.98400 |
| FGFR3c ligand binding and activation | 10 | 8.85e-01 | -2.65e-02 | 0.98400 |
| Signaling by Insulin receptor | 60 | 7.24e-01 | -2.64e-02 | 0.95900 |
| GPVI-mediated activation cascade | 25 | 8.20e-01 | 2.63e-02 | 0.96800 |
| HIV Infection | 155 | 5.75e-01 | 2.62e-02 | 0.94500 |
| RUNX3 regulates NOTCH signaling | 13 | 8.70e-01 | 2.61e-02 | 0.97800 |
| PIP3 activates AKT signaling | 210 | 5.21e-01 | 2.58e-02 | 0.94500 |
| Negative regulation of FGFR4 signaling | 23 | 8.34e-01 | -2.53e-02 | 0.96800 |
| Downstream signaling of activated FGFR3 | 20 | 8.45e-01 | 2.53e-02 | 0.97000 |
| RHO GTPases Activate ROCKs | 13 | 8.75e-01 | 2.52e-02 | 0.97800 |
| Post-translational modification: synthesis of GPI-anchored proteins | 67 | 7.25e-01 | 2.49e-02 | 0.95900 |
| TNFR2 non-canonical NF-kB pathway | 69 | 7.23e-01 | 2.47e-02 | 0.95900 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 22 | 8.42e-01 | -2.46e-02 | 0.96800 |
| Formation of Fibrin Clot (Clotting Cascade) | 31 | 8.14e-01 | 2.44e-02 | 0.96700 |
| SUMOylation of transcription cofactors | 33 | 8.09e-01 | -2.43e-02 | 0.96700 |
| Metabolism of polyamines | 42 | 7.86e-01 | 2.43e-02 | 0.96300 |
| Formation of the Early Elongation Complex | 19 | 8.55e-01 | 2.42e-02 | 0.97400 |
| Formation of the HIV-1 Early Elongation Complex | 19 | 8.55e-01 | 2.42e-02 | 0.97400 |
| Regulation of insulin secretion | 65 | 7.37e-01 | -2.42e-02 | 0.95900 |
| Activation of kainate receptors upon glutamate binding | 24 | 8.39e-01 | -2.40e-02 | 0.96800 |
| mRNA Splicing | 125 | 6.44e-01 | 2.40e-02 | 0.95900 |
| Intracellular signaling by second messengers | 243 | 5.23e-01 | 2.39e-02 | 0.94500 |
| Transcriptional Regulation by MECP2 | 48 | 7.77e-01 | 2.37e-02 | 0.96200 |
| Vpu mediated degradation of CD4 | 35 | 8.10e-01 | -2.35e-02 | 0.96700 |
| Glycosphingolipid metabolism | 31 | 8.22e-01 | 2.33e-02 | 0.96800 |
| Transcriptional regulation by RUNX2 | 84 | 7.13e-01 | 2.33e-02 | 0.95900 |
| Phosphorylation of the APC/C | 17 | 8.69e-01 | -2.32e-02 | 0.97800 |
| Assembly of the pre-replicative complex | 47 | 7.84e-01 | 2.31e-02 | 0.96300 |
| Cytochrome P450 - arranged by substrate type | 53 | 7.74e-01 | -2.28e-02 | 0.96200 |
| Carboxyterminal post-translational modifications of tubulin | 32 | 8.25e-01 | -2.26e-02 | 0.96800 |
| Signaling by Hippo | 17 | 8.72e-01 | 2.25e-02 | 0.97800 |
| Signaling by NOTCH4 | 62 | 7.60e-01 | 2.25e-02 | 0.96000 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 13 | 8.89e-01 | 2.24e-02 | 0.98500 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 55 | 7.76e-01 | -2.22e-02 | 0.96200 |
| Interleukin-6 family signaling | 20 | 8.64e-01 | -2.21e-02 | 0.97700 |
| Toll Like Receptor 4 (TLR4) Cascade | 98 | 7.05e-01 | 2.21e-02 | 0.95900 |
| B-WICH complex positively regulates rRNA expression | 21 | 8.61e-01 | -2.21e-02 | 0.97600 |
| NOD1/2 Signaling Pathway | 24 | 8.51e-01 | 2.21e-02 | 0.97300 |
| Glycerophospholipid biosynthesis | 91 | 7.16e-01 | 2.21e-02 | 0.95900 |
| Negative regulation of the PI3K/AKT network | 93 | 7.15e-01 | -2.19e-02 | 0.95900 |
| PKMTs methylate histone lysines | 32 | 8.31e-01 | 2.19e-02 | 0.96800 |
| Transcriptional regulation by RUNX1 | 136 | 6.65e-01 | -2.15e-02 | 0.95900 |
| Signal regulatory protein family interactions | 11 | 9.02e-01 | 2.15e-02 | 0.98800 |
| Signaling by WNT | 209 | 5.93e-01 | 2.15e-02 | 0.94500 |
| Energy dependent regulation of mTOR by LKB1-AMPK | 21 | 8.65e-01 | -2.14e-02 | 0.97700 |
| Phase II - Conjugation of compounds | 79 | 7.45e-01 | -2.12e-02 | 0.95900 |
| Formation of TC-NER Pre-Incision Complex | 33 | 8.34e-01 | 2.11e-02 | 0.96800 |
| RAB geranylgeranylation | 41 | 8.16e-01 | -2.11e-02 | 0.96700 |
| Metabolism of lipids | 560 | 4.10e-01 | 2.05e-02 | 0.94500 |
| DNA Replication | 95 | 7.31e-01 | 2.04e-02 | 0.95900 |
| Glycolysis | 55 | 7.94e-01 | 2.04e-02 | 0.96400 |
| PLC beta mediated events | 45 | 8.13e-01 | -2.04e-02 | 0.96700 |
| Transport of small molecules | 557 | 4.17e-01 | 2.02e-02 | 0.94500 |
| Metabolism of amino acids and derivatives | 250 | 5.83e-01 | -2.02e-02 | 0.94500 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 31 | 8.47e-01 | -2.01e-02 | 0.97100 |
| G alpha (q) signalling events | 168 | 6.54e-01 | -2.01e-02 | 0.95900 |
| Hedgehog ligand biogenesis | 45 | 8.16e-01 | -2.00e-02 | 0.96700 |
| PI3K/AKT Signaling in Cancer | 87 | 7.47e-01 | -2.00e-02 | 0.95900 |
| Cargo trafficking to the periciliary membrane | 37 | 8.33e-01 | -2.00e-02 | 0.96800 |
| VxPx cargo-targeting to cilium | 15 | 8.95e-01 | 1.97e-02 | 0.98600 |
| Elastic fibre formation | 33 | 8.45e-01 | -1.97e-02 | 0.97000 |
| Anti-inflammatory response favouring Leishmania parasite infection | 141 | 6.87e-01 | -1.97e-02 | 0.95900 |
| Leishmania parasite growth and survival | 141 | 6.87e-01 | -1.97e-02 | 0.95900 |
| Dopamine Neurotransmitter Release Cycle | 16 | 8.92e-01 | -1.96e-02 | 0.98500 |
| PIWI-interacting RNA (piRNA) biogenesis | 18 | 8.86e-01 | -1.96e-02 | 0.98400 |
| Signaling by the B Cell Receptor (BCR) | 81 | 7.61e-01 | 1.96e-02 | 0.96000 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 64 | 7.90e-01 | -1.92e-02 | 0.96400 |
| Interleukin receptor SHC signaling | 19 | 8.85e-01 | -1.92e-02 | 0.98400 |
| Downstream TCR signaling | 66 | 7.90e-01 | 1.90e-02 | 0.96400 |
| Signaling by FGFR2 in disease | 29 | 8.61e-01 | -1.88e-02 | 0.97600 |
| TP53 Regulates Transcription of Cell Death Genes | 30 | 8.60e-01 | 1.86e-02 | 0.97600 |
| Infectious disease | 519 | 4.74e-01 | 1.85e-02 | 0.94500 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | 20 | 8.86e-01 | -1.85e-02 | 0.98400 |
| Signaling by NOTCH1 | 58 | 8.08e-01 | -1.84e-02 | 0.96700 |
| Acyl chain remodelling of PI | 14 | 9.06e-01 | -1.83e-02 | 0.98900 |
| Ion transport by P-type ATPases | 42 | 8.38e-01 | -1.82e-02 | 0.96800 |
| G alpha (i) signalling events | 292 | 5.98e-01 | -1.80e-02 | 0.94500 |
| Peroxisomal protein import | 48 | 8.29e-01 | 1.80e-02 | 0.96800 |
| Mitochondrial translation | 62 | 8.07e-01 | 1.80e-02 | 0.96700 |
| Listeria monocytogenes entry into host cells | 14 | 9.08e-01 | 1.78e-02 | 0.99100 |
| Metabolism of steroids | 118 | 7.40e-01 | -1.77e-02 | 0.95900 |
| Glycosaminoglycan metabolism | 93 | 7.72e-01 | -1.74e-02 | 0.96200 |
| Creation of C4 and C2 activators | 17 | 9.02e-01 | 1.73e-02 | 0.98800 |
| Peptide ligand-binding receptors | 149 | 7.17e-01 | -1.72e-02 | 0.95900 |
| Metabolism of water-soluble vitamins and cofactors | 90 | 7.79e-01 | -1.72e-02 | 0.96200 |
| Acyl chain remodelling of PE | 19 | 8.97e-01 | -1.71e-02 | 0.98600 |
| Nucleobase catabolism | 29 | 8.74e-01 | 1.70e-02 | 0.97800 |
| TP53 Regulates Transcription of DNA Repair Genes | 38 | 8.57e-01 | 1.69e-02 | 0.97400 |
| Phospholipase C-mediated cascade: FGFR1 | 14 | 9.14e-01 | -1.67e-02 | 0.99300 |
| Generic Transcription Pathway | 737 | 4.49e-01 | 1.66e-02 | 0.94500 |
| Clathrin-mediated endocytosis | 107 | 7.70e-01 | -1.64e-02 | 0.96200 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | 18 | 9.05e-01 | -1.63e-02 | 0.98900 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 18 | 9.05e-01 | -1.63e-02 | 0.98900 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | 57 | 8.32e-01 | 1.63e-02 | 0.96800 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 57 | 8.32e-01 | 1.63e-02 | 0.96800 |
| CDT1 association with the CDC6:ORC:origin complex | 40 | 8.60e-01 | 1.61e-02 | 0.97600 |
| DNA Double-Strand Break Repair | 93 | 7.91e-01 | 1.60e-02 | 0.96400 |
| HIV Life Cycle | 95 | 7.93e-01 | -1.56e-02 | 0.96400 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 10 | 9.34e-01 | 1.52e-02 | 0.99500 |
| Hh mutants that don't undergo autocatalytic processing are degraded by ERAD | 36 | 8.75e-01 | -1.52e-02 | 0.97800 |
| Degradation of DVL | 39 | 8.71e-01 | 1.51e-02 | 0.97800 |
| Immune System | 1495 | 3.46e-01 | 1.49e-02 | 0.92900 |
| MAPK family signaling cascades | 240 | 7.00e-01 | 1.45e-02 | 0.95900 |
| Apoptotic cleavage of cell adhesion proteins | 10 | 9.37e-01 | 1.45e-02 | 0.99500 |
| SLC transporter disorders | 80 | 8.28e-01 | 1.41e-02 | 0.96800 |
| RHO GTPases Activate NADPH Oxidases | 20 | 9.14e-01 | 1.40e-02 | 0.99300 |
| ADORA2B mediated anti-inflammatory cytokines production | 108 | 8.05e-01 | -1.37e-02 | 0.96700 |
| Purine catabolism | 16 | 9.25e-01 | -1.35e-02 | 0.99500 |
| Macroautophagy | 85 | 8.32e-01 | -1.33e-02 | 0.96800 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) | 30 | 9.00e-01 | -1.33e-02 | 0.98700 |
| RNA Polymerase III Chain Elongation | 11 | 9.39e-01 | 1.33e-02 | 0.99500 |
| Activation of the TFAP2 (AP-2) family of transcription factors | 10 | 9.42e-01 | -1.33e-02 | 0.99500 |
| EPHB-mediated forward signaling | 24 | 9.10e-01 | 1.33e-02 | 0.99100 |
| Uptake and function of anthrax toxins | 11 | 9.39e-01 | 1.33e-02 | 0.99500 |
| Defective CFTR causes cystic fibrosis | 40 | 8.86e-01 | -1.31e-02 | 0.98400 |
| Organelle biogenesis and maintenance | 209 | 7.45e-01 | 1.31e-02 | 0.95900 |
| Ubiquitin-dependent degradation of Cyclin D | 36 | 8.93e-01 | 1.30e-02 | 0.98500 |
| ABC-family proteins mediated transport | 71 | 8.51e-01 | -1.29e-02 | 0.97300 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 54 | 8.70e-01 | 1.29e-02 | 0.97800 |
| Vesicle-mediated transport | 504 | 6.27e-01 | -1.27e-02 | 0.95500 |
| Platelet activation, signaling and aggregation | 204 | 7.58e-01 | 1.25e-02 | 0.96000 |
| Regulation of Apoptosis | 36 | 8.98e-01 | -1.24e-02 | 0.98600 |
| SUMOylation of transcription factors | 14 | 9.37e-01 | 1.22e-02 | 0.99500 |
| Signaling by NTRK3 (TRKC) | 15 | 9.35e-01 | 1.21e-02 | 0.99500 |
| Degradation of GLI2 by the proteasome | 41 | 8.94e-01 | 1.20e-02 | 0.98600 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 11 | 9.46e-01 | -1.19e-02 | 0.99500 |
| Degradation of GLI1 by the proteasome | 40 | 8.98e-01 | -1.17e-02 | 0.98600 |
| Abacavir transport and metabolism | 10 | 9.50e-01 | 1.16e-02 | 0.99500 |
| Signaling by FGFR in disease | 46 | 8.93e-01 | 1.15e-02 | 0.98500 |
| TRAF6 mediated NF-kB activation | 20 | 9.30e-01 | -1.14e-02 | 0.99500 |
| Class I MHC mediated antigen processing & presentation | 274 | 7.49e-01 | -1.13e-02 | 0.95900 |
| Metabolism of cofactors | 18 | 9.36e-01 | 1.10e-02 | 0.99500 |
| Vitamin B5 (pantothenate) metabolism | 13 | 9.47e-01 | 1.07e-02 | 0.99500 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 10 | 9.53e-01 | -1.07e-02 | 0.99500 |
| Caspase activation via Death Receptors in the presence of ligand | 14 | 9.46e-01 | -1.05e-02 | 0.99500 |
| GLI3 is processed to GLI3R by the proteasome | 40 | 9.09e-01 | 1.05e-02 | 0.99100 |
| Negative regulation of MAPK pathway | 34 | 9.16e-01 | 1.04e-02 | 0.99300 |
| Acyl chain remodelling of PC | 21 | 9.34e-01 | -1.04e-02 | 0.99500 |
| Hemostasis | 465 | 7.04e-01 | -1.04e-02 | 0.95900 |
| PI-3K cascade:FGFR3 | 15 | 9.45e-01 | -1.03e-02 | 0.99500 |
| Vif-mediated degradation of APOBEC3G | 35 | 9.17e-01 | 1.02e-02 | 0.99300 |
| C-type lectin receptors (CLRs) | 98 | 8.64e-01 | -1.00e-02 | 0.97700 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 38 | 9.15e-01 | 1.00e-02 | 0.99300 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 64 | 8.90e-01 | -9.96e-03 | 0.98500 |
| Integrin signaling | 23 | 9.35e-01 | 9.89e-03 | 0.99500 |
| Diseases of signal transduction by growth factor receptors and second messengers | 295 | 7.72e-01 | 9.84e-03 | 0.96200 |
| Switching of origins to a post-replicative state | 66 | 8.91e-01 | -9.77e-03 | 0.98500 |
| Metabolism | 1538 | 5.36e-01 | 9.67e-03 | 0.94500 |
| Regulation of RUNX2 expression and activity | 50 | 9.13e-01 | -8.97e-03 | 0.99300 |
| L1CAM interactions | 84 | 8.89e-01 | 8.85e-03 | 0.98500 |
| CaM pathway | 28 | 9.37e-01 | -8.57e-03 | 0.99500 |
| Calmodulin induced events | 28 | 9.37e-01 | -8.57e-03 | 0.99500 |
| Toll-like Receptor Cascades | 114 | 8.79e-01 | 8.26e-03 | 0.98100 |
| FLT3 Signaling | 218 | 8.37e-01 | -8.12e-03 | 0.96800 |
| TCF dependent signaling in response to WNT | 132 | 8.74e-01 | -8.01e-03 | 0.97800 |
| The phototransduction cascade | 24 | 9.46e-01 | 8.00e-03 | 0.99500 |
| Leishmania infection | 208 | 8.47e-01 | -7.78e-03 | 0.97100 |
| Adenylate cyclase activating pathway | 10 | 9.66e-01 | -7.77e-03 | 0.99500 |
| Negative regulation of MET activity | 14 | 9.60e-01 | -7.74e-03 | 0.99500 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 19 | 9.54e-01 | 7.71e-03 | 0.99500 |
| p53-Dependent G1 DNA Damage Response | 46 | 9.29e-01 | -7.60e-03 | 0.99500 |
| p53-Dependent G1/S DNA damage checkpoint | 46 | 9.29e-01 | -7.60e-03 | 0.99500 |
| SHC-mediated cascade:FGFR1 | 18 | 9.57e-01 | 7.40e-03 | 0.99500 |
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 34 | 9.40e-01 | -7.40e-03 | 0.99500 |
| p53-Independent DNA Damage Response | 34 | 9.40e-01 | -7.40e-03 | 0.99500 |
| p53-Independent G1/S DNA damage checkpoint | 34 | 9.40e-01 | -7.40e-03 | 0.99500 |
| Disease | 1091 | 6.87e-01 | 7.35e-03 | 0.95900 |
| PI3K events in ERBB2 signaling | 13 | 9.64e-01 | 7.25e-03 | 0.99500 |
| Reversible hydration of carbon dioxide | 12 | 9.66e-01 | -7.18e-03 | 0.99500 |
| Thromboxane signalling through TP receptor | 16 | 9.60e-01 | -7.17e-03 | 0.99500 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | 12 | 9.66e-01 | -7.13e-03 | 0.99500 |
| Downstream signaling of activated FGFR1 | 27 | 9.49e-01 | 7.12e-03 | 0.99500 |
| Removal of the Flap Intermediate from the C-strand | 12 | 9.66e-01 | 7.01e-03 | 0.99500 |
| Signaling by NOTCH3 | 40 | 9.42e-01 | -6.63e-03 | 0.99500 |
| Metabolism of proteins | 1369 | 6.89e-01 | 6.59e-03 | 0.95900 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 34 | 9.47e-01 | 6.56e-03 | 0.99500 |
| Nuclear Receptor transcription pathway | 48 | 9.38e-01 | -6.45e-03 | 0.99500 |
| Adaptive Immune System | 531 | 8.09e-01 | -6.19e-03 | 0.96700 |
| Regulation of TP53 Degradation | 30 | 9.53e-01 | 6.16e-03 | 0.99500 |
| WNT ligand biogenesis and trafficking | 21 | 9.65e-01 | 5.54e-03 | 0.99500 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 28 | 9.60e-01 | -5.51e-03 | 0.99500 |
| RNA Polymerase II Pre-transcription Events | 53 | 9.45e-01 | -5.49e-03 | 0.99500 |
| Signaling by FGFR4 | 31 | 9.58e-01 | 5.43e-03 | 0.99500 |
| RNA Polymerase III Abortive And Retractive Initiation | 27 | 9.61e-01 | 5.39e-03 | 0.99500 |
| RNA Polymerase III Transcription | 27 | 9.61e-01 | 5.39e-03 | 0.99500 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 30 | 9.60e-01 | -5.32e-03 | 0.99500 |
| Regulation of PTEN stability and activity | 47 | 9.50e-01 | -5.29e-03 | 0.99500 |
| Cellular Senescence | 103 | 9.27e-01 | -5.24e-03 | 0.99500 |
| Signaling by Nuclear Receptors | 193 | 9.05e-01 | -4.99e-03 | 0.98900 |
| Asymmetric localization of PCP proteins | 48 | 9.54e-01 | -4.84e-03 | 0.99500 |
| Ion channel transport | 131 | 9.25e-01 | -4.77e-03 | 0.99500 |
| G-protein beta:gamma signalling | 23 | 9.69e-01 | -4.73e-03 | 0.99500 |
| Netrin-1 signaling | 41 | 9.59e-01 | -4.63e-03 | 0.99500 |
| ESR-mediated signaling | 130 | 9.36e-01 | 4.07e-03 | 0.99500 |
| Innate Immune System | 741 | 8.54e-01 | 4.01e-03 | 0.97400 |
| Signal Transduction | 1944 | 7.80e-01 | -3.94e-03 | 0.96200 |
| RAF/MAP kinase cascade | 205 | 9.23e-01 | -3.92e-03 | 0.99500 |
| Activation of GABAB receptors | 34 | 9.68e-01 | -3.92e-03 | 0.99500 |
| GABA B receptor activation | 34 | 9.68e-01 | -3.92e-03 | 0.99500 |
| Intra-Golgi traffic | 34 | 9.69e-01 | 3.87e-03 | 0.99500 |
| Fcgamma receptor (FCGR) dependent phagocytosis | 76 | 9.55e-01 | -3.74e-03 | 0.99500 |
| HCMV Early Events | 44 | 9.66e-01 | 3.74e-03 | 0.99500 |
| Fatty acids | 11 | 9.83e-01 | -3.65e-03 | 1.00000 |
| Rho GTPase cycle | 118 | 9.46e-01 | 3.62e-03 | 0.99500 |
| Membrane Trafficking | 473 | 8.97e-01 | -3.49e-03 | 0.98600 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 13 | 9.84e-01 | 3.28e-03 | 1.00000 |
| Disorders of transmembrane transporters | 133 | 9.48e-01 | -3.26e-03 | 0.99500 |
| Constitutive Signaling by AKT1 E17K in Cancer | 22 | 9.79e-01 | 3.20e-03 | 1.00000 |
| Post-translational protein modification | 1001 | 8.67e-01 | -3.17e-03 | 0.97800 |
| Dectin-2 family | 15 | 9.83e-01 | -3.16e-03 | 1.00000 |
| GPCR ligand binding | 342 | 9.21e-01 | -3.14e-03 | 0.99500 |
| Synthesis of substrates in N-glycan biosythesis | 52 | 9.69e-01 | 3.13e-03 | 0.99500 |
| G1/S DNA Damage Checkpoints | 47 | 9.71e-01 | 3.10e-03 | 0.99600 |
| Transcriptional Regulation by VENTX | 32 | 9.76e-01 | 3.04e-03 | 1.00000 |
| Nervous system development | 412 | 9.18e-01 | 2.96e-03 | 0.99400 |
| Translesion synthesis by POLK | 12 | 9.87e-01 | -2.67e-03 | 1.00000 |
| Negative regulation of FGFR2 signaling | 26 | 9.82e-01 | -2.52e-03 | 1.00000 |
| Synthesis of DNA | 88 | 9.68e-01 | 2.51e-03 | 0.99500 |
| Signaling by NOTCH | 140 | 9.60e-01 | -2.43e-03 | 0.99500 |
| Aflatoxin activation and detoxification | 16 | 9.87e-01 | 2.36e-03 | 1.00000 |
| Interleukin-10 signaling | 33 | 9.82e-01 | 2.28e-03 | 1.00000 |
| SCF-beta-TrCP mediated degradation of Emi1 | 38 | 9.81e-01 | 2.18e-03 | 1.00000 |
| Inactivation, recovery and regulation of the phototransduction cascade | 23 | 9.86e-01 | 2.14e-03 | 1.00000 |
| Synthesis of PIPs at the Golgi membrane | 14 | 9.91e-01 | 1.70e-03 | 1.00000 |
| Deposition of new CENPA-containing nucleosomes at the centromere | 16 | 9.91e-01 | -1.66e-03 | 1.00000 |
| Nucleosome assembly | 16 | 9.91e-01 | -1.66e-03 | 1.00000 |
| Transcriptional regulation by RUNX3 | 76 | 9.80e-01 | 1.64e-03 | 1.00000 |
| Signaling by Receptor Tyrosine Kinases | 392 | 9.57e-01 | -1.60e-03 | 0.99500 |
| Removal of the Flap Intermediate | 11 | 9.94e-01 | -1.37e-03 | 1.00000 |
| FCERI mediated NF-kB activation | 55 | 9.87e-01 | -1.29e-03 | 1.00000 |
| Pyruvate metabolism and Citric Acid (TCA) cycle | 39 | 9.90e-01 | 1.17e-03 | 1.00000 |
| Ras activation upon Ca2+ influx through NMDA receptor | 16 | 9.94e-01 | 1.14e-03 | 1.00000 |
| G beta:gamma signalling through CDC42 | 13 | 9.95e-01 | 1.10e-03 | 1.00000 |
| Cilium Assembly | 148 | 9.83e-01 | 1.01e-03 | 1.00000 |
| Aquaporin-mediated transport | 42 | 9.92e-01 | -8.86e-04 | 1.00000 |
| Synthesis, secretion, and deacylation of Ghrelin | 14 | 9.96e-01 | -8.44e-04 | 1.00000 |
| MAPK1/MAPK3 signaling | 210 | 9.92e-01 | -4.24e-04 | 1.00000 |
| FRS-mediated FGFR1 signaling | 19 | 9.97e-01 | 4.21e-04 | 1.00000 |
| Axon guidance | 391 | 9.89e-01 | -3.98e-04 | 1.00000 |
| Interferon gamma signaling | 57 | 9.96e-01 | 3.89e-04 | 1.00000 |
| Vasopressin regulates renal water homeostasis via Aquaporins | 34 | 9.97e-01 | -3.18e-04 | 1.00000 |
| Developmental Biology | 716 | 9.90e-01 | 2.81e-04 | 1.00000 |
| Regulation of TP53 Expression and Degradation | 31 | 9.99e-01 | 1.37e-04 | 1.00000 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 55 | 9.99e-01 | 1.27e-04 | 1.00000 |
| Autophagy | 96 | 9.99e-01 | -8.76e-05 | 1.00000 |
| Cell-extracellular matrix interactions | 14 | 1.00e+00 | -7.72e-05 | 1.00000 |
| Negative regulation of NOTCH4 signaling | 38 | 1.00e+00 | 4.18e-05 | 1.00000 |
TRAF6 mediated IRF7 activation
| 1184 | |
|---|---|
| set | TRAF6 mediated IRF7 activation |
| setSize | 28 |
| pANOVA | 1.26e-06 |
| s.dist | 0.529 |
| p.adjustANOVA | 0.00168 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IRF7 | 6525 |
| IFNA1 | 6455 |
| IFNA10 | 6455 |
| IFNA14 | 6455 |
| IFNA16 | 6455 |
| IFNA17 | 6455 |
| IFNA2 | 6455 |
| IFNA21 | 6455 |
| IFNA4 | 6455 |
| IFNA5 | 6455 |
| IFNA6 | 6455 |
| IFNA7 | 6455 |
| IFNA8 | 6455 |
| TRIM25 | 6238 |
| SIKE1 | 5591 |
| CREBBP | 4905 |
| MAVS | 4637 |
| EP300 | 4577 |
| TBK1 | 3656 |
| TANK | 3276 |
| GeneID | Gene Rank |
|---|---|
| IRF7 | 6525 |
| IFNA1 | 6455 |
| IFNA10 | 6455 |
| IFNA14 | 6455 |
| IFNA16 | 6455 |
| IFNA17 | 6455 |
| IFNA2 | 6455 |
| IFNA21 | 6455 |
| IFNA4 | 6455 |
| IFNA5 | 6455 |
| IFNA6 | 6455 |
| IFNA7 | 6455 |
| IFNA8 | 6455 |
| TRIM25 | 6238 |
| SIKE1 | 5591 |
| CREBBP | 4905 |
| MAVS | 4637 |
| EP300 | 4577 |
| TBK1 | 3656 |
| TANK | 3276 |
| IFIH1 | 2048 |
| RNF135 | 1160 |
| IRF3 | 817 |
| TRAF2 | -232 |
| TRAF6 | -412 |
| IKBKE | -2494 |
| DDX58 | -4737 |
| IFNB1 | -5873 |
Condensation of Prophase Chromosomes
| 201 | |
|---|---|
| set | Condensation of Prophase Chromosomes |
| setSize | 10 |
| pANOVA | 0.00677 |
| s.dist | 0.495 |
| p.adjustANOVA | 0.637 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PHF8 | 6782 |
| MCPH1 | 5957 |
| CDK1 | 5332 |
| RB1 | 5239 |
| SMC4 | 4810 |
| CCNB1 | 4806 |
| H2AFX | 3215 |
| SET | 2312 |
| NCAPG2 | 6 |
| NCAPH2 | -2548 |
| GeneID | Gene Rank |
|---|---|
| PHF8 | 6782 |
| MCPH1 | 5957 |
| CDK1 | 5332 |
| RB1 | 5239 |
| SMC4 | 4810 |
| CCNB1 | 4806 |
| H2AFX | 3215 |
| SET | 2312 |
| NCAPG2 | 6 |
| NCAPH2 | -2548 |
Regulation of IFNA signaling
| 933 | |
|---|---|
| set | Regulation of IFNA signaling |
| setSize | 23 |
| pANOVA | 0.000121 |
| s.dist | 0.463 |
| p.adjustANOVA | 0.0808 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IFNA1 | 6455.0 |
| IFNA10 | 6455.0 |
| IFNA14 | 6455.0 |
| IFNA16 | 6455.0 |
| IFNA17 | 6455.0 |
| IFNA2 | 6455.0 |
| IFNA21 | 6455.0 |
| IFNA4 | 6455.0 |
| IFNA5 | 6455.0 |
| IFNA6 | 6455.0 |
| IFNA7 | 6455.0 |
| IFNA8 | 6455.0 |
| PTPN1 | 5377.0 |
| IFNAR2 | 4782.0 |
| SOCS3 | 4354.0 |
| USP18 | 1630.5 |
| STAT1 | 1477.0 |
| IFNAR1 | 574.0 |
| TYK2 | -1243.0 |
| JAK1 | -2079.0 |
| GeneID | Gene Rank |
|---|---|
| IFNA1 | 6455.0 |
| IFNA10 | 6455.0 |
| IFNA14 | 6455.0 |
| IFNA16 | 6455.0 |
| IFNA17 | 6455.0 |
| IFNA2 | 6455.0 |
| IFNA21 | 6455.0 |
| IFNA4 | 6455.0 |
| IFNA5 | 6455.0 |
| IFNA6 | 6455.0 |
| IFNA7 | 6455.0 |
| IFNA8 | 6455.0 |
| PTPN1 | 5377.0 |
| IFNAR2 | 4782.0 |
| SOCS3 | 4354.0 |
| USP18 | 1630.5 |
| STAT1 | 1477.0 |
| IFNAR1 | 574.0 |
| TYK2 | -1243.0 |
| JAK1 | -2079.0 |
| PTPN11 | -2745.0 |
| IFNB1 | -5873.0 |
| PTPN6 | -6221.0 |
alpha-linolenic (omega3) and linoleic (omega6) acid metabolism
| 1303 | |
|---|---|
| set | alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
| setSize | 11 |
| pANOVA | 0.00908 |
| s.dist | 0.454 |
| p.adjustANOVA | 0.637 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| FADS2 | 6603 |
| ACOT8 | 6366 |
| ELOVL2 | 5022 |
| ELOVL3 | 4709 |
| HSD17B4 | 4554 |
| SCP2 | 4022 |
| FADS1 | 3739 |
| ELOVL5 | 1053 |
| ELOVL1 | 633 |
| ACOX1 | 459 |
| ACSL1 | -730 |
| GeneID | Gene Rank |
|---|---|
| FADS2 | 6603 |
| ACOT8 | 6366 |
| ELOVL2 | 5022 |
| ELOVL3 | 4709 |
| HSD17B4 | 4554 |
| SCP2 | 4022 |
| FADS1 | 3739 |
| ELOVL5 | 1053 |
| ELOVL1 | 633 |
| ACOX1 | 459 |
| ACSL1 | -730 |
alpha-linolenic acid (ALA) metabolism
| 1304 | |
|---|---|
| set | alpha-linolenic acid (ALA) metabolism |
| setSize | 11 |
| pANOVA | 0.00908 |
| s.dist | 0.454 |
| p.adjustANOVA | 0.637 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| FADS2 | 6603 |
| ACOT8 | 6366 |
| ELOVL2 | 5022 |
| ELOVL3 | 4709 |
| HSD17B4 | 4554 |
| SCP2 | 4022 |
| FADS1 | 3739 |
| ELOVL5 | 1053 |
| ELOVL1 | 633 |
| ACOX1 | 459 |
| ACSL1 | -730 |
| GeneID | Gene Rank |
|---|---|
| FADS2 | 6603 |
| ACOT8 | 6366 |
| ELOVL2 | 5022 |
| ELOVL3 | 4709 |
| HSD17B4 | 4554 |
| SCP2 | 4022 |
| FADS1 | 3739 |
| ELOVL5 | 1053 |
| ELOVL1 | 633 |
| ACOX1 | 459 |
| ACSL1 | -730 |
Heme degradation
| 494 | |
|---|---|
| set | Heme degradation |
| setSize | 15 |
| pANOVA | 0.00232 |
| s.dist | 0.454 |
| p.adjustANOVA | 0.362 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HMOX2 | 6853.0 |
| ABCG2 | 6672.0 |
| ABCC1 | 6183.0 |
| GSTA1 | 5192.5 |
| SLCO1B1 | 4741.0 |
| SLCO1B3 | 4741.0 |
| BLVRA | 4703.0 |
| ABCC2 | 3920.0 |
| SLCO2B1 | 3857.0 |
| ALB | 3645.0 |
| UGT1A4 | 2922.0 |
| BLVRB | 926.0 |
| HMOX1 | -968.0 |
| GUSB | -1232.0 |
| FABP1 | -2505.0 |
| GeneID | Gene Rank |
|---|---|
| HMOX2 | 6853.0 |
| ABCG2 | 6672.0 |
| ABCC1 | 6183.0 |
| GSTA1 | 5192.5 |
| SLCO1B1 | 4741.0 |
| SLCO1B3 | 4741.0 |
| BLVRA | 4703.0 |
| ABCC2 | 3920.0 |
| SLCO2B1 | 3857.0 |
| ALB | 3645.0 |
| UGT1A4 | 2922.0 |
| BLVRB | 926.0 |
| HMOX1 | -968.0 |
| GUSB | -1232.0 |
| FABP1 | -2505.0 |
E2F mediated regulation of DNA replication
| 311 | |
|---|---|
| set | E2F mediated regulation of DNA replication |
| setSize | 18 |
| pANOVA | 0.00109 |
| s.dist | 0.445 |
| p.adjustANOVA | 0.292 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PPP2R1A | 6383.0 |
| ORC2 | 6251.0 |
| PPP2R1B | 5533.0 |
| E2F1 | 5502.0 |
| CDK1 | 5332.0 |
| RB1 | 5239.0 |
| ORC1 | 4978.0 |
| CCNB1 | 4806.0 |
| PPP2CA | 4097.0 |
| POLA2 | 3942.0 |
| TFDP2 | 3548.0 |
| POLA1 | 2821.0 |
| ORC3 | 2699.0 |
| ORC4 | 2545.0 |
| PRIM2 | 1786.0 |
| PPP2CB | 787.0 |
| PRIM1 | -2478.0 |
| TFDP1 | -5401.5 |
| GeneID | Gene Rank |
|---|---|
| PPP2R1A | 6383.0 |
| ORC2 | 6251.0 |
| PPP2R1B | 5533.0 |
| E2F1 | 5502.0 |
| CDK1 | 5332.0 |
| RB1 | 5239.0 |
| ORC1 | 4978.0 |
| CCNB1 | 4806.0 |
| PPP2CA | 4097.0 |
| POLA2 | 3942.0 |
| TFDP2 | 3548.0 |
| POLA1 | 2821.0 |
| ORC3 | 2699.0 |
| ORC4 | 2545.0 |
| PRIM2 | 1786.0 |
| PPP2CB | 787.0 |
| PRIM1 | -2478.0 |
| TFDP1 | -5401.5 |
WNT5A-dependent internalization of FZD2, FZD5 and ROR2
| 1295 | |
|---|---|
| set | WNT5A-dependent internalization of FZD2, FZD5 and ROR2 |
| setSize | 12 |
| pANOVA | 0.0129 |
| s.dist | 0.415 |
| p.adjustANOVA | 0.748 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ROR1 | 7079 |
| CLTC | 6403 |
| AP2M1 | 6005 |
| ROR2 | 5359 |
| AP2A2 | 3939 |
| FZD2 | 3036 |
| FZD5 | 2992 |
| AP2S1 | 2697 |
| CLTB | 2691 |
| WNT5A | 277 |
| AP2A1 | -1653 |
| CLTA | -2393 |
| GeneID | Gene Rank |
|---|---|
| ROR1 | 7079 |
| CLTC | 6403 |
| AP2M1 | 6005 |
| ROR2 | 5359 |
| AP2A2 | 3939 |
| FZD2 | 3036 |
| FZD5 | 2992 |
| AP2S1 | 2697 |
| CLTB | 2691 |
| WNT5A | 277 |
| AP2A1 | -1653 |
| CLTA | -2393 |
Regulation of signaling by NODAL
| 974 | |
|---|---|
| set | Regulation of signaling by NODAL |
| setSize | 10 |
| pANOVA | 0.0441 |
| s.dist | -0.368 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DAND5 | -6416.0 |
| ACVR1C | -6058.0 |
| TDGF1 | -5972.0 |
| ACVR2A | -3417.0 |
| CER1 | -3309.0 |
| ACVR2B | -2649.0 |
| NODAL | -2480.0 |
| LEFTY1 | 1375.5 |
| LEFTY2 | 1375.5 |
| ACVR1B | 3631.0 |
| GeneID | Gene Rank |
|---|---|
| DAND5 | -6416.0 |
| ACVR1C | -6058.0 |
| TDGF1 | -5972.0 |
| ACVR2A | -3417.0 |
| CER1 | -3309.0 |
| ACVR2B | -2649.0 |
| NODAL | -2480.0 |
| LEFTY1 | 1375.5 |
| LEFTY2 | 1375.5 |
| ACVR1B | 3631.0 |
Regulation of PTEN mRNA translation
| 940 | |
|---|---|
| set | Regulation of PTEN mRNA translation |
| setSize | 11 |
| pANOVA | 0.0348 |
| s.dist | 0.368 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PTEN | 7020 |
| MIR214 | 6581 |
| CNOT6L | 6050 |
| AGO2 | 5601 |
| AGO4 | 4382 |
| MOV10 | 3708 |
| AGO3 | 1416 |
| TNRC6B | 1372 |
| AGO1 | 1256 |
| TNRC6C | -2939 |
| MIR26A1 | -4639 |
| GeneID | Gene Rank |
|---|---|
| PTEN | 7020 |
| MIR214 | 6581 |
| CNOT6L | 6050 |
| AGO2 | 5601 |
| AGO4 | 4382 |
| MOV10 | 3708 |
| AGO3 | 1416 |
| TNRC6B | 1372 |
| AGO1 | 1256 |
| TNRC6C | -2939 |
| MIR26A1 | -4639 |
Inhibition of replication initiation of damaged DNA by RB1/E2F1
| 523 | |
|---|---|
| set | Inhibition of replication initiation of damaged DNA by RB1/E2F1 |
| setSize | 12 |
| pANOVA | 0.0316 |
| s.dist | 0.358 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PPP2R1A | 6383.0 |
| PPP2R1B | 5533.0 |
| E2F1 | 5502.0 |
| RB1 | 5239.0 |
| PPP2CA | 4097.0 |
| POLA2 | 3942.0 |
| TFDP2 | 3548.0 |
| POLA1 | 2821.0 |
| PRIM2 | 1786.0 |
| PPP2CB | 787.0 |
| PRIM1 | -2478.0 |
| TFDP1 | -5401.5 |
| GeneID | Gene Rank |
|---|---|
| PPP2R1A | 6383.0 |
| PPP2R1B | 5533.0 |
| E2F1 | 5502.0 |
| RB1 | 5239.0 |
| PPP2CA | 4097.0 |
| POLA2 | 3942.0 |
| TFDP2 | 3548.0 |
| POLA1 | 2821.0 |
| PRIM2 | 1786.0 |
| PPP2CB | 787.0 |
| PRIM1 | -2478.0 |
| TFDP1 | -5401.5 |
Golgi Cisternae Pericentriolar Stack Reorganization
| 468 | |
|---|---|
| set | Golgi Cisternae Pericentriolar Stack Reorganization |
| setSize | 11 |
| pANOVA | 0.0417 |
| s.dist | 0.355 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MAPK1 | 5777 |
| USO1 | 5407 |
| CDK1 | 5332 |
| CCNB1 | 4806 |
| RAB2A | 3107 |
| BLZF1 | 2791 |
| RAB1A | 2718 |
| MAPK3 | 932 |
| GORASP2 | 19 |
| GOLGA2 | -846 |
| RAB1B | -1220 |
| GeneID | Gene Rank |
|---|---|
| MAPK1 | 5777 |
| USO1 | 5407 |
| CDK1 | 5332 |
| CCNB1 | 4806 |
| RAB2A | 3107 |
| BLZF1 | 2791 |
| RAB1A | 2718 |
| MAPK3 | 932 |
| GORASP2 | 19 |
| GOLGA2 | -846 |
| RAB1B | -1220 |
Tandem pore domain potassium channels
| 1190 | |
|---|---|
| set | Tandem pore domain potassium channels |
| setSize | 11 |
| pANOVA | 0.0426 |
| s.dist | 0.353 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KCNK3 | 4958 |
| KCNK1 | 4901 |
| KCNK13 | 4750 |
| KCNK9 | 4546 |
| KCNK16 | 2339 |
| KCNK18 | 2253 |
| KCNK2 | 2151 |
| KCNK6 | 1494 |
| KCNK7 | 1039 |
| KCNK4 | 477 |
| KCNK10 | -204 |
| GeneID | Gene Rank |
|---|---|
| KCNK3 | 4958 |
| KCNK1 | 4901 |
| KCNK13 | 4750 |
| KCNK9 | 4546 |
| KCNK16 | 2339 |
| KCNK18 | 2253 |
| KCNK2 | 2151 |
| KCNK6 | 1494 |
| KCNK7 | 1039 |
| KCNK4 | 477 |
| KCNK10 | -204 |
Scavenging of heme from plasma
| 1034 | |
|---|---|
| set | Scavenging of heme from plasma |
| setSize | 10 |
| pANOVA | 0.0539 |
| s.dist | -0.352 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IGHA1 | -6546.5 |
| IGHA2 | -6546.5 |
| AMBP | -5240.0 |
| LRP1 | -4439.0 |
| HP | -3698.5 |
| HPR | -3698.5 |
| APOL1 | -3470.5 |
| APOA1 | 273.0 |
| ALB | 3645.0 |
| HPX | 6888.0 |
| GeneID | Gene Rank |
|---|---|
| IGHA1 | -6546.5 |
| IGHA2 | -6546.5 |
| AMBP | -5240.0 |
| LRP1 | -4439.0 |
| HP | -3698.5 |
| HPR | -3698.5 |
| APOL1 | -3470.5 |
| APOA1 | 273.0 |
| ALB | 3645.0 |
| HPX | 6888.0 |
Metabolism of porphyrins
| 632 | |
|---|---|
| set | Metabolism of porphyrins |
| setSize | 25 |
| pANOVA | 0.00245 |
| s.dist | 0.35 |
| p.adjustANOVA | 0.362 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| FECH | 7038.0 |
| HMOX2 | 6853.0 |
| UROD | 6775.0 |
| ABCG2 | 6672.0 |
| ABCC1 | 6183.0 |
| HMBS | 5775.0 |
| GSTA1 | 5192.5 |
| SLCO1B1 | 4741.0 |
| SLCO1B3 | 4741.0 |
| BLVRA | 4703.0 |
| PPOX | 4263.0 |
| ABCC2 | 3920.0 |
| SLCO2B1 | 3857.0 |
| ALB | 3645.0 |
| CPOX | 2932.0 |
| UGT1A4 | 2922.0 |
| ALAS2 | 2270.0 |
| BLVRB | 926.0 |
| HMOX1 | -968.0 |
| GUSB | -1232.0 |
| GeneID | Gene Rank |
|---|---|
| FECH | 7038.0 |
| HMOX2 | 6853.0 |
| UROD | 6775.0 |
| ABCG2 | 6672.0 |
| ABCC1 | 6183.0 |
| HMBS | 5775.0 |
| GSTA1 | 5192.5 |
| SLCO1B1 | 4741.0 |
| SLCO1B3 | 4741.0 |
| BLVRA | 4703.0 |
| PPOX | 4263.0 |
| ABCC2 | 3920.0 |
| SLCO2B1 | 3857.0 |
| ALB | 3645.0 |
| CPOX | 2932.0 |
| UGT1A4 | 2922.0 |
| ALAS2 | 2270.0 |
| BLVRB | 926.0 |
| HMOX1 | -968.0 |
| GUSB | -1232.0 |
| COX15 | -1348.0 |
| ALAS1 | -2042.0 |
| FABP1 | -2505.0 |
| ALAD | -4717.0 |
| UROS | -5932.0 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA
| 1268 | |
|---|---|
| set | Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA |
| setSize | 11 |
| pANOVA | 0.0514 |
| s.dist | 0.339 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DCP2 | 6773 |
| YWHAB | 6616 |
| EXOSC2 | 6470 |
| EXOSC3 | 6265 |
| EXOSC9 | 5962 |
| TNPO1 | 4077 |
| EXOSC8 | 3970 |
| DCP1A | 2988 |
| EXOSC7 | -3933 |
| XRN1 | -4965 |
| DIS3 | -6579 |
| GeneID | Gene Rank |
|---|---|
| DCP2 | 6773 |
| YWHAB | 6616 |
| EXOSC2 | 6470 |
| EXOSC3 | 6265 |
| EXOSC9 | 5962 |
| TNPO1 | 4077 |
| EXOSC8 | 3970 |
| DCP1A | 2988 |
| EXOSC7 | -3933 |
| XRN1 | -4965 |
| DIS3 | -6579 |
FOXO-mediated transcription of cell death genes
| 371 | |
|---|---|
| set | FOXO-mediated transcription of cell death genes |
| setSize | 13 |
| pANOVA | 0.0369 |
| s.dist | 0.334 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NFYC | 6760 |
| CREBBP | 4905 |
| EP300 | 4577 |
| CITED2 | 4485 |
| FOXO3 | 3593 |
| FOXO4 | 3114 |
| STK11 | 3052 |
| NFYA | 2597 |
| NFYB | 2349 |
| BCL2L11 | 1954 |
| BCL6 | 1435 |
| FASLG | -2643 |
| PINK1 | -3960 |
| GeneID | Gene Rank |
|---|---|
| NFYC | 6760 |
| CREBBP | 4905 |
| EP300 | 4577 |
| CITED2 | 4485 |
| FOXO3 | 3593 |
| FOXO4 | 3114 |
| STK11 | 3052 |
| NFYA | 2597 |
| NFYB | 2349 |
| BCL2L11 | 1954 |
| BCL6 | 1435 |
| FASLG | -2643 |
| PINK1 | -3960 |
Citric acid cycle (TCA cycle)
| 183 | |
|---|---|
| set | Citric acid cycle (TCA cycle) |
| setSize | 15 |
| pANOVA | 0.0272 |
| s.dist | 0.329 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NNT | 6718 |
| SUCLA2 | 5881 |
| DLST | 5763 |
| DLD | 5656 |
| ME2 | 5436 |
| ME3 | 4994 |
| SDHA | 4617 |
| IDH3B | 3491 |
| SUCLG1 | 1999 |
| ACO2 | 485 |
| SDHB | -22 |
| IDH3G | -294 |
| IDH2 | -817 |
| FH | -1462 |
| CS | -5774 |
| GeneID | Gene Rank |
|---|---|
| NNT | 6718 |
| SUCLA2 | 5881 |
| DLST | 5763 |
| DLD | 5656 |
| ME2 | 5436 |
| ME3 | 4994 |
| SDHA | 4617 |
| IDH3B | 3491 |
| SUCLG1 | 1999 |
| ACO2 | 485 |
| SDHB | -22 |
| IDH3G | -294 |
| IDH2 | -817 |
| FH | -1462 |
| CS | -5774 |
Cyclin A/B1/B2 associated events during G2/M transition
| 216 | |
|---|---|
| set | Cyclin A/B1/B2 associated events during G2/M transition |
| setSize | 13 |
| pANOVA | 0.0404 |
| s.dist | 0.328 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PPP2R1A | 6383 |
| PPP2R1B | 5533 |
| CDK1 | 5332 |
| XPO1 | 5255 |
| CCNB1 | 4806 |
| CCNA1 | 4136 |
| PPP2CA | 4097 |
| CDC25A | 3589 |
| CCNA2 | 3048 |
| PPP2CB | 787 |
| CDC25B | -2367 |
| CCNH | -2608 |
| FOXM1 | -6310 |
| GeneID | Gene Rank |
|---|---|
| PPP2R1A | 6383 |
| PPP2R1B | 5533 |
| CDK1 | 5332 |
| XPO1 | 5255 |
| CCNB1 | 4806 |
| CCNA1 | 4136 |
| PPP2CA | 4097 |
| CDC25A | 3589 |
| CCNA2 | 3048 |
| PPP2CB | 787 |
| CDC25B | -2367 |
| CCNH | -2608 |
| FOXM1 | -6310 |
Nucleotide-like (purinergic) receptors
| 739 | |
|---|---|
| set | Nucleotide-like (purinergic) receptors |
| setSize | 11 |
| pANOVA | 0.0613 |
| s.dist | -0.326 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ADORA2B | -6681 |
| ADORA2A | -5578 |
| P2RY6 | -5049 |
| P2RY12 | -4899 |
| GPR17 | -4380 |
| P2RY13 | -4278 |
| P2RY1 | -3476 |
| P2RY4 | -2565 |
| P2RY14 | 2440 |
| P2RY2 | 4310 |
| ADORA1 | 7041 |
| GeneID | Gene Rank |
|---|---|
| ADORA2B | -6681 |
| ADORA2A | -5578 |
| P2RY6 | -5049 |
| P2RY12 | -4899 |
| GPR17 | -4380 |
| P2RY13 | -4278 |
| P2RY1 | -3476 |
| P2RY4 | -2565 |
| P2RY14 | 2440 |
| P2RY2 | 4310 |
| ADORA1 | 7041 |
Phase 4 - resting membrane potential
| 795 | |
|---|---|
| set | Phase 4 - resting membrane potential |
| setSize | 17 |
| pANOVA | 0.0201 |
| s.dist | 0.326 |
| p.adjustANOVA | 0.808 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KCNK12 | 6813 |
| KCNK5 | 6472 |
| KCNJ4 | 5785 |
| KCNJ12 | 5102 |
| KCNK3 | 4958 |
| KCNK1 | 4901 |
| KCNK13 | 4750 |
| KCNK9 | 4546 |
| KCNK16 | 2339 |
| KCNK18 | 2253 |
| KCNK2 | 2151 |
| KCNK6 | 1494 |
| KCNK7 | 1039 |
| KCNK4 | 477 |
| KCNK10 | -204 |
| KCNJ14 | -5443 |
| KCNK15 | -6315 |
| GeneID | Gene Rank |
|---|---|
| KCNK12 | 6813 |
| KCNK5 | 6472 |
| KCNJ4 | 5785 |
| KCNJ12 | 5102 |
| KCNK3 | 4958 |
| KCNK1 | 4901 |
| KCNK13 | 4750 |
| KCNK9 | 4546 |
| KCNK16 | 2339 |
| KCNK18 | 2253 |
| KCNK2 | 2151 |
| KCNK6 | 1494 |
| KCNK7 | 1039 |
| KCNK4 | 477 |
| KCNK10 | -204 |
| KCNJ14 | -5443 |
| KCNK15 | -6315 |
Diseases associated with the TLR signaling cascade
| 284 | |
|---|---|
| set | Diseases associated with the TLR signaling cascade |
| setSize | 18 |
| pANOVA | 0.0189 |
| s.dist | -0.32 |
| p.adjustANOVA | 0.808 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LY96 | -5820 |
| TRAF3 | -5705 |
| TLR2 | -5525 |
| CHUK | -5160 |
| IKBKB | -4573 |
| TLR5 | -4539 |
| TLR6 | -4458 |
| NFKB2 | -2503 |
| CD36 | -2327 |
| CD14 | -1831 |
| TLR1 | -1546 |
| RELA | -1430 |
| TIRAP | -787 |
| IKBKG | -291 |
| NFKB1 | -49 |
| TLR3 | 2029 |
| NFKBIA | 3567 |
| TICAM1 | 3918 |
| GeneID | Gene Rank |
|---|---|
| LY96 | -5820 |
| TRAF3 | -5705 |
| TLR2 | -5525 |
| CHUK | -5160 |
| IKBKB | -4573 |
| TLR5 | -4539 |
| TLR6 | -4458 |
| NFKB2 | -2503 |
| CD36 | -2327 |
| CD14 | -1831 |
| TLR1 | -1546 |
| RELA | -1430 |
| TIRAP | -787 |
| IKBKG | -291 |
| NFKB1 | -49 |
| TLR3 | 2029 |
| NFKBIA | 3567 |
| TICAM1 | 3918 |
Diseases of Immune System
| 287 | |
|---|---|
| set | Diseases of Immune System |
| setSize | 18 |
| pANOVA | 0.0189 |
| s.dist | -0.32 |
| p.adjustANOVA | 0.808 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LY96 | -5820 |
| TRAF3 | -5705 |
| TLR2 | -5525 |
| CHUK | -5160 |
| IKBKB | -4573 |
| TLR5 | -4539 |
| TLR6 | -4458 |
| NFKB2 | -2503 |
| CD36 | -2327 |
| CD14 | -1831 |
| TLR1 | -1546 |
| RELA | -1430 |
| TIRAP | -787 |
| IKBKG | -291 |
| NFKB1 | -49 |
| TLR3 | 2029 |
| NFKBIA | 3567 |
| TICAM1 | 3918 |
| GeneID | Gene Rank |
|---|---|
| LY96 | -5820 |
| TRAF3 | -5705 |
| TLR2 | -5525 |
| CHUK | -5160 |
| IKBKB | -4573 |
| TLR5 | -4539 |
| TLR6 | -4458 |
| NFKB2 | -2503 |
| CD36 | -2327 |
| CD14 | -1831 |
| TLR1 | -1546 |
| RELA | -1430 |
| TIRAP | -787 |
| IKBKG | -291 |
| NFKB1 | -49 |
| TLR3 | 2029 |
| NFKBIA | 3567 |
| TICAM1 | 3918 |
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters
| 693 | |
|---|---|
| set | Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters |
| setSize | 16 |
| pANOVA | 0.0282 |
| s.dist | 0.317 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| B2M | 7065 |
| AP2M1 | 6005 |
| CD28 | 5298 |
| AP1M2 | 4762 |
| AP1G1 | 4230 |
| AP1S2 | 4179 |
| PACS1 | 4002 |
| AP2A2 | 3939 |
| CD4 | 3343 |
| AP2S1 | 2697 |
| LCK | 2589 |
| AP1B1 | 711 |
| AP1S3 | -1419 |
| AP2A1 | -1653 |
| AP1S1 | -2670 |
| AP1M1 | -5358 |
| GeneID | Gene Rank |
|---|---|
| B2M | 7065 |
| AP2M1 | 6005 |
| CD28 | 5298 |
| AP1M2 | 4762 |
| AP1G1 | 4230 |
| AP1S2 | 4179 |
| PACS1 | 4002 |
| AP2A2 | 3939 |
| CD4 | 3343 |
| AP2S1 | 2697 |
| LCK | 2589 |
| AP1B1 | 711 |
| AP1S3 | -1419 |
| AP2A1 | -1653 |
| AP1S1 | -2670 |
| AP1M1 | -5358 |
Eicosanoid ligand-binding receptors
| 331 | |
|---|---|
| set | Eicosanoid ligand-binding receptors |
| setSize | 10 |
| pANOVA | 0.0844 |
| s.dist | -0.315 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PTGER3 | -6088 |
| TBXA2R | -5179 |
| PTGDR2 | -5042 |
| GPR17 | -4380 |
| LTB4R | -3049 |
| PTGIR | -2311 |
| PTGFR | -1107 |
| PTGER1 | 321 |
| LTB4R2 | 3254 |
| PTGER4 | 3302 |
| GeneID | Gene Rank |
|---|---|
| PTGER3 | -6088 |
| TBXA2R | -5179 |
| PTGDR2 | -5042 |
| GPR17 | -4380 |
| LTB4R | -3049 |
| PTGIR | -2311 |
| PTGFR | -1107 |
| PTGER1 | 321 |
| LTB4R2 | 3254 |
| PTGER4 | 3302 |
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects
| 24 | |
|---|---|
| set | Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects |
| setSize | 13 |
| pANOVA | 0.0513 |
| s.dist | 0.312 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CDKN1B | 5654.0 |
| E2F1 | 5502.0 |
| RB1 | 5239.0 |
| E2F2 | 4129.0 |
| CDKN1A | 4027.0 |
| CDK4 | 3960.0 |
| TFDP2 | 3548.0 |
| E2F3 | 2654.0 |
| CCND3 | 2174.0 |
| CCND1 | 1432.0 |
| CDKN1C | 1212.0 |
| CCNE1 | -3898.0 |
| TFDP1 | -5401.5 |
| GeneID | Gene Rank |
|---|---|
| CDKN1B | 5654.0 |
| E2F1 | 5502.0 |
| RB1 | 5239.0 |
| E2F2 | 4129.0 |
| CDKN1A | 4027.0 |
| CDK4 | 3960.0 |
| TFDP2 | 3548.0 |
| E2F3 | 2654.0 |
| CCND3 | 2174.0 |
| CCND1 | 1432.0 |
| CDKN1C | 1212.0 |
| CCNE1 | -3898.0 |
| TFDP1 | -5401.5 |
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3)
| 256 | |
|---|---|
| set | Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) |
| setSize | 13 |
| pANOVA | 0.0513 |
| s.dist | 0.312 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CDKN1B | 5654.0 |
| E2F1 | 5502.0 |
| RB1 | 5239.0 |
| E2F2 | 4129.0 |
| CDKN1A | 4027.0 |
| CDK4 | 3960.0 |
| TFDP2 | 3548.0 |
| E2F3 | 2654.0 |
| CCND3 | 2174.0 |
| CCND1 | 1432.0 |
| CDKN1C | 1212.0 |
| CCNE1 | -3898.0 |
| TFDP1 | -5401.5 |
| GeneID | Gene Rank |
|---|---|
| CDKN1B | 5654.0 |
| E2F1 | 5502.0 |
| RB1 | 5239.0 |
| E2F2 | 4129.0 |
| CDKN1A | 4027.0 |
| CDK4 | 3960.0 |
| TFDP2 | 3548.0 |
| E2F3 | 2654.0 |
| CCND3 | 2174.0 |
| CCND1 | 1432.0 |
| CDKN1C | 1212.0 |
| CCNE1 | -3898.0 |
| TFDP1 | -5401.5 |
TP53 Regulates Transcription of Death Receptors and Ligands
| 1177 | |
|---|---|
| set | TP53 Regulates Transcription of Death Receptors and Ligands |
| setSize | 10 |
| pANOVA | 0.0887 |
| s.dist | 0.311 |
| p.adjustANOVA | 0.853 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IGFBP3 | 6562.0 |
| TP63 | 5421.0 |
| TNFRSF10A | 3418.5 |
| TNFRSF10B | 3418.5 |
| TNFRSF10C | 3418.5 |
| TNFRSF10D | 3418.5 |
| PPP1R13B | 2560.0 |
| TP73 | 365.0 |
| TP53 | 340.0 |
| TMEM219 | -5750.0 |
| GeneID | Gene Rank |
|---|---|
| IGFBP3 | 6562.0 |
| TP63 | 5421.0 |
| TNFRSF10A | 3418.5 |
| TNFRSF10B | 3418.5 |
| TNFRSF10C | 3418.5 |
| TNFRSF10D | 3418.5 |
| PPP1R13B | 2560.0 |
| TP73 | 365.0 |
| TP53 | 340.0 |
| TMEM219 | -5750.0 |
HS-GAG biosynthesis
| 485 | |
|---|---|
| set | HS-GAG biosynthesis |
| setSize | 22 |
| pANOVA | 0.0124 |
| s.dist | -0.308 |
| p.adjustANOVA | 0.748 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HS3ST5 | -6763 |
| HS3ST1 | -5600 |
| GPC3 | -5370 |
| EXT2 | -5263 |
| SDC4 | -5131 |
| HSPG2 | -4993 |
| GPC6 | -4732 |
| NDST4 | -4669 |
| GPC1 | -4511 |
| NDST2 | -4223 |
| HS3ST2 | -3484 |
| NDST1 | -3408 |
| AGRN | -3290 |
| NDST3 | -2290 |
| SDC3 | -1679 |
| HS6ST3 | -1533 |
| SLC35D2 | 702 |
| EXT1 | 1077 |
| GLCE | 3307 |
| HS6ST1 | 5813 |
| GeneID | Gene Rank |
|---|---|
| HS3ST5 | -6763 |
| HS3ST1 | -5600 |
| GPC3 | -5370 |
| EXT2 | -5263 |
| SDC4 | -5131 |
| HSPG2 | -4993 |
| GPC6 | -4732 |
| NDST4 | -4669 |
| GPC1 | -4511 |
| NDST2 | -4223 |
| HS3ST2 | -3484 |
| NDST1 | -3408 |
| AGRN | -3290 |
| NDST3 | -2290 |
| SDC3 | -1679 |
| HS6ST3 | -1533 |
| SLC35D2 | 702 |
| EXT1 | 1077 |
| GLCE | 3307 |
| HS6ST1 | 5813 |
| GPC2 | 6036 |
| GPC5 | 6503 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
| 251 | |
|---|---|
| set | Defective EXT1 causes exostoses 1, TRPS2 and CHDS |
| setSize | 11 |
| pANOVA | 0.0821 |
| s.dist | -0.303 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GPC3 | -5370 |
| EXT2 | -5263 |
| SDC4 | -5131 |
| HSPG2 | -4993 |
| GPC6 | -4732 |
| GPC1 | -4511 |
| AGRN | -3290 |
| SDC3 | -1679 |
| EXT1 | 1077 |
| GPC2 | 6036 |
| GPC5 | 6503 |
| GeneID | Gene Rank |
|---|---|
| GPC3 | -5370 |
| EXT2 | -5263 |
| SDC4 | -5131 |
| HSPG2 | -4993 |
| GPC6 | -4732 |
| GPC1 | -4511 |
| AGRN | -3290 |
| SDC3 | -1679 |
| EXT1 | 1077 |
| GPC2 | 6036 |
| GPC5 | 6503 |
Defective EXT2 causes exostoses 2
| 252 | |
|---|---|
| set | Defective EXT2 causes exostoses 2 |
| setSize | 11 |
| pANOVA | 0.0821 |
| s.dist | -0.303 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GPC3 | -5370 |
| EXT2 | -5263 |
| SDC4 | -5131 |
| HSPG2 | -4993 |
| GPC6 | -4732 |
| GPC1 | -4511 |
| AGRN | -3290 |
| SDC3 | -1679 |
| EXT1 | 1077 |
| GPC2 | 6036 |
| GPC5 | 6503 |
| GeneID | Gene Rank |
|---|---|
| GPC3 | -5370 |
| EXT2 | -5263 |
| SDC4 | -5131 |
| HSPG2 | -4993 |
| GPC6 | -4732 |
| GPC1 | -4511 |
| AGRN | -3290 |
| SDC3 | -1679 |
| EXT1 | 1077 |
| GPC2 | 6036 |
| GPC5 | 6503 |
Regulation of TP53 Activity through Methylation
| 951 | |
|---|---|
| set | Regulation of TP53 Activity through Methylation |
| setSize | 11 |
| pANOVA | 0.0823 |
| s.dist | -0.303 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UBA52 | -5940 |
| SMYD2 | -5861 |
| PRMT5 | -4537 |
| MDM2 | -4532 |
| ATM | -4492 |
| L3MBTL1 | -3551 |
| EHMT2 | -2103 |
| TP53 | 340 |
| MDM4 | 1353 |
| EHMT1 | 3409 |
| EP300 | 4577 |
| GeneID | Gene Rank |
|---|---|
| UBA52 | -5940 |
| SMYD2 | -5861 |
| PRMT5 | -4537 |
| MDM2 | -4532 |
| ATM | -4492 |
| L3MBTL1 | -3551 |
| EHMT2 | -2103 |
| TP53 | 340 |
| MDM4 | 1353 |
| EHMT1 | 3409 |
| EP300 | 4577 |
Diseases of DNA repair
| 286 | |
|---|---|
| set | Diseases of DNA repair |
| setSize | 10 |
| pANOVA | 0.109 |
| s.dist | 0.293 |
| p.adjustANOVA | 0.885 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NEIL3 | 6805 |
| PMS2 | 5219 |
| MUTYH | 4387 |
| MSH6 | 4160 |
| MSH3 | 3478 |
| MLH1 | 3139 |
| NTHL1 | 2128 |
| MSH2 | -2420 |
| OGG1 | -2458 |
| NEIL1 | -2521 |
| GeneID | Gene Rank |
|---|---|
| NEIL3 | 6805 |
| PMS2 | 5219 |
| MUTYH | 4387 |
| MSH6 | 4160 |
| MSH3 | 3478 |
| MLH1 | 3139 |
| NTHL1 | 2128 |
| MSH2 | -2420 |
| OGG1 | -2458 |
| NEIL1 | -2521 |
The role of Nef in HIV-1 replication and disease pathogenesis
| 1204 | |
|---|---|
| set | The role of Nef in HIV-1 replication and disease pathogenesis |
| setSize | 23 |
| pANOVA | 0.0155 |
| s.dist | 0.291 |
| p.adjustANOVA | 0.768 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| B2M | 7065 |
| PAK2 | 6878 |
| AP2M1 | 6005 |
| RAC1 | 5939 |
| CD28 | 5298 |
| AP1M2 | 4762 |
| AP1G1 | 4230 |
| AP1S2 | 4179 |
| PACS1 | 4002 |
| AP2A2 | 3939 |
| ELMO1 | 3914 |
| FYN | 3558 |
| CD4 | 3343 |
| AP2S1 | 2697 |
| LCK | 2589 |
| AP1B1 | 711 |
| HCK | -525 |
| AP1S3 | -1419 |
| AP2A1 | -1653 |
| DOCK2 | -2344 |
| GeneID | Gene Rank |
|---|---|
| B2M | 7065 |
| PAK2 | 6878 |
| AP2M1 | 6005 |
| RAC1 | 5939 |
| CD28 | 5298 |
| AP1M2 | 4762 |
| AP1G1 | 4230 |
| AP1S2 | 4179 |
| PACS1 | 4002 |
| AP2A2 | 3939 |
| ELMO1 | 3914 |
| FYN | 3558 |
| CD4 | 3343 |
| AP2S1 | 2697 |
| LCK | 2589 |
| AP1B1 | 711 |
| HCK | -525 |
| AP1S3 | -1419 |
| AP2A1 | -1653 |
| DOCK2 | -2344 |
| AP1S1 | -2670 |
| CD247 | -4994 |
| AP1M1 | -5358 |
ER Quality Control Compartment (ERQC)
| 321 | |
|---|---|
| set | ER Quality Control Compartment (ERQC) |
| setSize | 12 |
| pANOVA | 0.0814 |
| s.dist | -0.291 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| EDEM3 | -6718 |
| SEL1L | -6254 |
| UGGT2 | -5986 |
| UBA52 | -5940 |
| EDEM2 | -4657 |
| TRIM13 | -4046 |
| AMFR | -3248 |
| UGGT1 | -3042 |
| OS9 | 1291 |
| MAN1B1 | 3940 |
| RNF139 | 5561 |
| SYVN1 | 6822 |
| GeneID | Gene Rank |
|---|---|
| EDEM3 | -6718 |
| SEL1L | -6254 |
| UGGT2 | -5986 |
| UBA52 | -5940 |
| EDEM2 | -4657 |
| TRIM13 | -4046 |
| AMFR | -3248 |
| UGGT1 | -3042 |
| OS9 | 1291 |
| MAN1B1 | 3940 |
| RNF139 | 5561 |
| SYVN1 | 6822 |
Synthesis of PC
| 1143 | |
|---|---|
| set | Synthesis of PC |
| setSize | 20 |
| pANOVA | 0.025 |
| s.dist | 0.29 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PCYT1B | 7023 |
| LPIN1 | 6540 |
| LPIN3 | 6297 |
| ABHD3 | 5426 |
| SLC44A5 | 5174 |
| SLC44A2 | 5000 |
| CSNK2A2 | 4151 |
| LPCAT1 | 3642 |
| PHOSPHO1 | 3138 |
| CHPT1 | 3054 |
| STARD7 | 2053 |
| SLC44A4 | 1768 |
| SLC44A1 | 1695 |
| ACHE | 1163 |
| MFSD2A | 943 |
| PEMT | 651 |
| LPIN2 | 233 |
| CHKA | -3142 |
| STARD10 | -4912 |
| PCTP | -6558 |
| GeneID | Gene Rank |
|---|---|
| PCYT1B | 7023 |
| LPIN1 | 6540 |
| LPIN3 | 6297 |
| ABHD3 | 5426 |
| SLC44A5 | 5174 |
| SLC44A2 | 5000 |
| CSNK2A2 | 4151 |
| LPCAT1 | 3642 |
| PHOSPHO1 | 3138 |
| CHPT1 | 3054 |
| STARD7 | 2053 |
| SLC44A4 | 1768 |
| SLC44A1 | 1695 |
| ACHE | 1163 |
| MFSD2A | 943 |
| PEMT | 651 |
| LPIN2 | 233 |
| CHKA | -3142 |
| STARD10 | -4912 |
| PCTP | -6558 |
Defective B4GALT7 causes EDS, progeroid type
| 248 | |
|---|---|
| set | Defective B4GALT7 causes EDS, progeroid type |
| setSize | 15 |
| pANOVA | 0.0546 |
| s.dist | -0.287 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CSPG4 | -6553 |
| B4GALT7 | -6313 |
| GPC3 | -5370 |
| DCN | -5348 |
| SDC4 | -5131 |
| HSPG2 | -4993 |
| GPC6 | -4732 |
| GPC1 | -4511 |
| AGRN | -3290 |
| SDC3 | -1679 |
| VCAN | -1017 |
| BGN | 2075 |
| GPC2 | 6036 |
| GPC5 | 6503 |
| CSPG5 | 6884 |
| GeneID | Gene Rank |
|---|---|
| CSPG4 | -6553 |
| B4GALT7 | -6313 |
| GPC3 | -5370 |
| DCN | -5348 |
| SDC4 | -5131 |
| HSPG2 | -4993 |
| GPC6 | -4732 |
| GPC1 | -4511 |
| AGRN | -3290 |
| SDC3 | -1679 |
| VCAN | -1017 |
| BGN | 2075 |
| GPC2 | 6036 |
| GPC5 | 6503 |
| CSPG5 | 6884 |
Norepinephrine Neurotransmitter Release Cycle
| 724 | |
|---|---|
| set | Norepinephrine Neurotransmitter Release Cycle |
| setSize | 12 |
| pANOVA | 0.0878 |
| s.dist | -0.285 |
| p.adjustANOVA | 0.853 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SLC22A2 | -6321 |
| RIMS1 | -5618 |
| PPFIA4 | -4545 |
| SYT1 | -4124 |
| STX1A | -3905 |
| UNC13B | -3618 |
| PPFIA3 | -2561 |
| SLC22A1 | -1671 |
| PPFIA1 | -245 |
| STXBP1 | 757 |
| RAB3A | 3959 |
| VAMP2 | 6110 |
| GeneID | Gene Rank |
|---|---|
| SLC22A2 | -6321 |
| RIMS1 | -5618 |
| PPFIA4 | -4545 |
| SYT1 | -4124 |
| STX1A | -3905 |
| UNC13B | -3618 |
| PPFIA3 | -2561 |
| SLC22A1 | -1671 |
| PPFIA1 | -245 |
| STXBP1 | 757 |
| RAB3A | 3959 |
| VAMP2 | 6110 |
Smooth Muscle Contraction
| 1126 | |
|---|---|
| set | Smooth Muscle Contraction |
| setSize | 29 |
| pANOVA | 0.00828 |
| s.dist | 0.283 |
| p.adjustANOVA | 0.637 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MYH11 | 7060 |
| PAK2 | 6878 |
| SORBS1 | 6816 |
| ACTA2 | 5686 |
| ACTG2 | 5570 |
| LMOD1 | 4490 |
| CAV3 | 4358 |
| MYL12A | 4300 |
| MYL7 | 4225 |
| TLN1 | 4158 |
| MYLK | 3664 |
| MYL6 | 3649 |
| ANXA6 | 3223 |
| ITGA1 | 3091 |
| MYL10 | 2982 |
| ANXA2 | 2930 |
| TPM3 | 2346 |
| TPM1 | 1855 |
| GUCY1A3 | 1731 |
| DYSF | 1613 |
| GeneID | Gene Rank |
|---|---|
| MYH11 | 7060 |
| PAK2 | 6878 |
| SORBS1 | 6816 |
| ACTA2 | 5686 |
| ACTG2 | 5570 |
| LMOD1 | 4490 |
| CAV3 | 4358 |
| MYL12A | 4300 |
| MYL7 | 4225 |
| TLN1 | 4158 |
| MYLK | 3664 |
| MYL6 | 3649 |
| ANXA6 | 3223 |
| ITGA1 | 3091 |
| MYL10 | 2982 |
| ANXA2 | 2930 |
| TPM3 | 2346 |
| TPM1 | 1855 |
| GUCY1A3 | 1731 |
| DYSF | 1613 |
| CALM1 | 1300 |
| ITGB5 | -573 |
| PXN | -582 |
| MYL12B | -1451 |
| TPM2 | -1516 |
| GUCY1B3 | -3166 |
| ANXA1 | -3255 |
| MYL9 | -3856 |
| CALD1 | -5956 |
Heme biosynthesis
| 493 | |
|---|---|
| set | Heme biosynthesis |
| setSize | 12 |
| pANOVA | 0.0916 |
| s.dist | 0.281 |
| p.adjustANOVA | 0.853 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| FECH | 7038 |
| UROD | 6775 |
| ABCG2 | 6672 |
| HMBS | 5775 |
| PPOX | 4263 |
| ALB | 3645 |
| CPOX | 2932 |
| ALAS2 | 2270 |
| COX15 | -1348 |
| ALAS1 | -2042 |
| ALAD | -4717 |
| UROS | -5932 |
| GeneID | Gene Rank |
|---|---|
| FECH | 7038 |
| UROD | 6775 |
| ABCG2 | 6672 |
| HMBS | 5775 |
| PPOX | 4263 |
| ALB | 3645 |
| CPOX | 2932 |
| ALAS2 | 2270 |
| COX15 | -1348 |
| ALAS1 | -2042 |
| ALAD | -4717 |
| UROS | -5932 |
Activation of PPARGC1A (PGC-1alpha) by phosphorylation
| 45 | |
|---|---|
| set | Activation of PPARGC1A (PGC-1alpha) by phosphorylation |
| setSize | 10 |
| pANOVA | 0.124 |
| s.dist | -0.281 |
| p.adjustANOVA | 0.885 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PRKAB1 | -5640 |
| PPARGC1A | -4684 |
| PRKAG1 | -4110 |
| PRKAG2 | -4038 |
| MAPK11 | -2706 |
| PRKAG3 | -2092 |
| PRKAA2 | -2065 |
| MAPK14 | 1261 |
| MAPK12 | 2975 |
| PRKAB2 | 3217 |
| GeneID | Gene Rank |
|---|---|
| PRKAB1 | -5640 |
| PPARGC1A | -4684 |
| PRKAG1 | -4110 |
| PRKAG2 | -4038 |
| MAPK11 | -2706 |
| PRKAG3 | -2092 |
| PRKAA2 | -2065 |
| MAPK14 | 1261 |
| MAPK12 | 2975 |
| PRKAB2 | 3217 |
Interferon alpha/beta signaling
| 542 | |
|---|---|
| set | Interferon alpha/beta signaling |
| setSize | 50 |
| pANOVA | 0.000644 |
| s.dist | 0.279 |
| p.adjustANOVA | 0.222 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| OAS1 | 6942 |
| IRF7 | 6525 |
| IFNA1 | 6455 |
| IFNA10 | 6455 |
| IFNA14 | 6455 |
| IFNA16 | 6455 |
| IFNA17 | 6455 |
| IFNA2 | 6455 |
| IFNA21 | 6455 |
| IFNA4 | 6455 |
| IFNA5 | 6455 |
| IFNA6 | 6455 |
| IFNA7 | 6455 |
| IFNA8 | 6455 |
| SAMHD1 | 6247 |
| PTPN1 | 5377 |
| MX1 | 4918 |
| IFNAR2 | 4782 |
| PSMB8 | 4384 |
| SOCS3 | 4354 |
| GeneID | Gene Rank |
|---|---|
| OAS1 | 6942.0 |
| IRF7 | 6525.0 |
| IFNA1 | 6455.0 |
| IFNA10 | 6455.0 |
| IFNA14 | 6455.0 |
| IFNA16 | 6455.0 |
| IFNA17 | 6455.0 |
| IFNA2 | 6455.0 |
| IFNA21 | 6455.0 |
| IFNA4 | 6455.0 |
| IFNA5 | 6455.0 |
| IFNA6 | 6455.0 |
| IFNA7 | 6455.0 |
| IFNA8 | 6455.0 |
| SAMHD1 | 6247.0 |
| PTPN1 | 5377.0 |
| MX1 | 4918.0 |
| IFNAR2 | 4782.0 |
| PSMB8 | 4384.0 |
| SOCS3 | 4354.0 |
| RSAD2 | 3229.0 |
| IRF9 | 3134.0 |
| OAS2 | 3000.0 |
| IFITM1 | 2641.0 |
| IFITM2 | 2641.0 |
| IFITM3 | 2641.0 |
| BST2 | 2518.0 |
| IRF1 | 2026.0 |
| USP18 | 1630.5 |
| STAT1 | 1477.0 |
| OAS3 | 1245.0 |
| ADAR | 1048.0 |
| IRF3 | 817.0 |
| IFNAR1 | 574.0 |
| EGR1 | 400.0 |
| XAF1 | -732.0 |
| IFI27 | -1064.0 |
| TYK2 | -1243.0 |
| IRF8 | -1433.0 |
| IFIT2 | -1925.0 |
| RNASEL | -2060.0 |
| JAK1 | -2079.0 |
| PTPN11 | -2745.0 |
| ISG20 | -3046.0 |
| IRF5 | -3455.0 |
| OASL | -4203.0 |
| IRF4 | -4529.0 |
| IRF6 | -4871.0 |
| IFNB1 | -5873.0 |
| PTPN6 | -6221.0 |
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway
| 1167 | |
|---|---|
| set | TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway |
| setSize | 12 |
| pANOVA | 0.097 |
| s.dist | 0.277 |
| p.adjustANOVA | 0.868 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TNFSF14 | 6742 |
| TNFRSF13C | 5844 |
| BIRC2 | 5444 |
| CD40LG | 4917 |
| TNFSF13B | 4453 |
| TNFSF11 | 3329 |
| TNFRSF11A | 3088 |
| CD40 | 1027 |
| BIRC3 | 67 |
| TRAF2 | -232 |
| LTBR | -4024 |
| TRAF3 | -5705 |
| GeneID | Gene Rank |
|---|---|
| TNFSF14 | 6742 |
| TNFRSF13C | 5844 |
| BIRC2 | 5444 |
| CD40LG | 4917 |
| TNFSF13B | 4453 |
| TNFSF11 | 3329 |
| TNFRSF11A | 3088 |
| CD40 | 1027 |
| BIRC3 | 67 |
| TRAF2 | -232 |
| LTBR | -4024 |
| TRAF3 | -5705 |
Activation of SMO
| 47 | |
|---|---|
| set | Activation of SMO |
| setSize | 10 |
| pANOVA | 0.131 |
| s.dist | -0.276 |
| p.adjustANOVA | 0.885 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| EVC2 | -6415 |
| IHH | -5051 |
| CDON | -4290 |
| IQCE | -3774 |
| GAS1 | -2657 |
| KIF3A | -1949 |
| ARRB1 | -1932 |
| EVC | 479 |
| DHH | 3489 |
| SMO | 4573 |
| GeneID | Gene Rank |
|---|---|
| EVC2 | -6415 |
| IHH | -5051 |
| CDON | -4290 |
| IQCE | -3774 |
| GAS1 | -2657 |
| KIF3A | -1949 |
| ARRB1 | -1932 |
| EVC | 479 |
| DHH | 3489 |
| SMO | 4573 |
Initiation of Nuclear Envelope (NE) Reformation
| 526 | |
|---|---|
| set | Initiation of Nuclear Envelope (NE) Reformation |
| setSize | 14 |
| pANOVA | 0.0745 |
| s.dist | 0.275 |
| p.adjustANOVA | 0.851 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PPP2R1A | 6383 |
| LMNB1 | 5835 |
| CDK1 | 5332 |
| VRK2 | 5172 |
| CCNB1 | 4806 |
| PPP2CA | 4097 |
| LMNA | 3792 |
| ANKLE2 | 3472 |
| LEMD2 | 1470 |
| SIRT2 | 83 |
| KPNB1 | -1007 |
| LBR | -1967 |
| TMPO | -2125 |
| VRK1 | -6372 |
| GeneID | Gene Rank |
|---|---|
| PPP2R1A | 6383 |
| LMNB1 | 5835 |
| CDK1 | 5332 |
| VRK2 | 5172 |
| CCNB1 | 4806 |
| PPP2CA | 4097 |
| LMNA | 3792 |
| ANKLE2 | 3472 |
| LEMD2 | 1470 |
| SIRT2 | 83 |
| KPNB1 | -1007 |
| LBR | -1967 |
| TMPO | -2125 |
| VRK1 | -6372 |
Synthesis of bile acids and bile salts via 27-hydroxycholesterol
| 1151 | |
|---|---|
| set | Synthesis of bile acids and bile salts via 27-hydroxycholesterol |
| setSize | 10 |
| pANOVA | 0.133 |
| s.dist | -0.275 |
| p.adjustANOVA | 0.885 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CYP8B1 | -6368 |
| CYP7A1 | -4085 |
| PTGIS | -2524 |
| RXRA | -2518 |
| NCOA2 | -1466 |
| NCOA1 | -1334 |
| CYP27A1 | -779 |
| HSD3B7 | -535 |
| NR1H4 | 1031 |
| AKR1D1 | 1120 |
| GeneID | Gene Rank |
|---|---|
| CYP8B1 | -6368 |
| CYP7A1 | -4085 |
| PTGIS | -2524 |
| RXRA | -2518 |
| NCOA2 | -1466 |
| NCOA1 | -1334 |
| CYP27A1 | -779 |
| HSD3B7 | -535 |
| NR1H4 | 1031 |
| AKR1D1 | 1120 |
Cleavage of the damaged purine
| 191 | |
|---|---|
| set | Cleavage of the damaged purine |
| setSize | 10 |
| pANOVA | 0.135 |
| s.dist | 0.273 |
| p.adjustANOVA | 0.885 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NEIL3 | 6805 |
| TERF1 | 4628 |
| MUTYH | 4387 |
| TERF2 | 3703 |
| H2AFX | 3215 |
| MPG | 1693 |
| ACD | 1227 |
| POT1 | -389 |
| TINF2 | -2250 |
| OGG1 | -2458 |
| GeneID | Gene Rank |
|---|---|
| NEIL3 | 6805 |
| TERF1 | 4628 |
| MUTYH | 4387 |
| TERF2 | 3703 |
| H2AFX | 3215 |
| MPG | 1693 |
| ACD | 1227 |
| POT1 | -389 |
| TINF2 | -2250 |
| OGG1 | -2458 |
Depurination
| 269 | |
|---|---|
| set | Depurination |
| setSize | 10 |
| pANOVA | 0.135 |
| s.dist | 0.273 |
| p.adjustANOVA | 0.885 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NEIL3 | 6805 |
| TERF1 | 4628 |
| MUTYH | 4387 |
| TERF2 | 3703 |
| H2AFX | 3215 |
| MPG | 1693 |
| ACD | 1227 |
| POT1 | -389 |
| TINF2 | -2250 |
| OGG1 | -2458 |
| GeneID | Gene Rank |
|---|---|
| NEIL3 | 6805 |
| TERF1 | 4628 |
| MUTYH | 4387 |
| TERF2 | 3703 |
| H2AFX | 3215 |
| MPG | 1693 |
| ACD | 1227 |
| POT1 | -389 |
| TINF2 | -2250 |
| OGG1 | -2458 |
Recognition and association of DNA glycosylase with site containing an affected purine
| 916 | |
|---|---|
| set | Recognition and association of DNA glycosylase with site containing an affected purine |
| setSize | 10 |
| pANOVA | 0.135 |
| s.dist | 0.273 |
| p.adjustANOVA | 0.885 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NEIL3 | 6805 |
| TERF1 | 4628 |
| MUTYH | 4387 |
| TERF2 | 3703 |
| H2AFX | 3215 |
| MPG | 1693 |
| ACD | 1227 |
| POT1 | -389 |
| TINF2 | -2250 |
| OGG1 | -2458 |
| GeneID | Gene Rank |
|---|---|
| NEIL3 | 6805 |
| TERF1 | 4628 |
| MUTYH | 4387 |
| TERF2 | 3703 |
| H2AFX | 3215 |
| MPG | 1693 |
| ACD | 1227 |
| POT1 | -389 |
| TINF2 | -2250 |
| OGG1 | -2458 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation
| 442 | |
|---|---|
| set | Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation |
| setSize | 25 |
| pANOVA | 0.0185 |
| s.dist | 0.272 |
| p.adjustANOVA | 0.808 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PAK2 | 6878.0 |
| RAP1B | 6508.0 |
| HNRNPF | 6411.0 |
| SERPINB2 | 6061.0 |
| TALDO1 | 6058.0 |
| LMNB1 | 5835.0 |
| RALA | 5608.0 |
| PITPNA | 5434.0 |
| CNN2 | 5282.0 |
| GSTA2 | 5192.5 |
| IL10 | 4850.0 |
| LCP1 | 4548.0 |
| STAT4 | 3508.0 |
| ANXA2 | 2930.0 |
| IFNG | 2530.0 |
| CA1 | 2039.0 |
| PDCD4 | 1598.0 |
| MIF | -746.0 |
| SNRPA1 | -2947.0 |
| HSPA9 | -3292.0 |
| GeneID | Gene Rank |
|---|---|
| PAK2 | 6878.0 |
| RAP1B | 6508.0 |
| HNRNPF | 6411.0 |
| SERPINB2 | 6061.0 |
| TALDO1 | 6058.0 |
| LMNB1 | 5835.0 |
| RALA | 5608.0 |
| PITPNA | 5434.0 |
| CNN2 | 5282.0 |
| GSTA2 | 5192.5 |
| IL10 | 4850.0 |
| LCP1 | 4548.0 |
| STAT4 | 3508.0 |
| ANXA2 | 2930.0 |
| IFNG | 2530.0 |
| CA1 | 2039.0 |
| PDCD4 | 1598.0 |
| MIF | -746.0 |
| SNRPA1 | -2947.0 |
| HSPA9 | -3292.0 |
| GSTO1 | -3541.0 |
| MTAP | -3688.5 |
| PSME2 | -4032.0 |
| CDC42 | -5214.0 |
| PPIA | -6637.0 |
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