date generated: 2024-01-11
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 | |
|---|---|
| A1BG | -0.1281221 |
| A1BG-AS1 | -0.1265037 |
| A1CF | -0.2257970 |
| A2M | -0.0016135 |
| A2M-AS1 | 1.3166603 |
| A2ML1 | -0.3595390 |
Here are some metrics about the input data profile:
| Profile metrics | |
|---|---|
| num_genesets | 2656 |
| num_genes_in_profile | 21625 |
| duplicated_genes_present | 0 |
| num_profile_genes_in_sets | 10357 |
| num_profile_genes_not_in_sets | 11268 |
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 | 2656 |
| num_genesets_excluded | 1052 |
| num_genesets_included | 1604 |
Significance is calculated by -log10(p-value). All points shown are FDR<0.05.
Significance is calculated by -log10(p-value). Top N sets shown irrespective of FDR.
Top N= 50 gene sets
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| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Regulation of gene expression in endocrine-committed (NEUROG3+) progenitor cells | 5 | 1.76e-03 | 0.808 | 1.71e-02 |
| Regulation of gene expression in early pancreatic precursor cells | 8 | 1.42e-04 | 0.777 | 2.93e-03 |
| Formation of lateral plate mesoderm | 5 | 3.27e-03 | 0.760 | 2.70e-02 |
| Free fatty acid receptors | 5 | 4.13e-03 | 0.740 | 3.18e-02 |
| Formation of intermediate mesoderm | 8 | 1.73e-03 | 0.639 | 1.69e-02 |
| Formation of the ureteric bud | 21 | 5.43e-07 | 0.631 | 1.96e-05 |
| Thyroxine biosynthesis | 10 | 5.98e-04 | 0.627 | 8.25e-03 |
| Transcriptional regulation of testis differentiation | 12 | 2.05e-04 | 0.619 | 3.97e-03 |
| Acrosome Reaction and Sperm:Oocyte Membrane Binding | 6 | 1.17e-02 | -0.594 | 7.01e-02 |
| Electric Transmission Across Gap Junctions | 5 | 2.16e-02 | 0.593 | 1.14e-01 |
| Transmission across Electrical Synapses | 5 | 2.16e-02 | 0.593 | 1.14e-01 |
| Defective LFNG causes SCDO3 | 5 | 2.46e-02 | 0.580 | 1.25e-01 |
| Formation of the anterior neural plate | 10 | 1.79e-03 | 0.570 | 1.71e-02 |
| Cobalamin (Cbl) metabolism | 7 | 9.39e-03 | -0.567 | 6.02e-02 |
| Specification of the neural plate border | 16 | 9.64e-05 | 0.563 | 2.10e-03 |
| Hyaluronan biosynthesis and export | 5 | 3.10e-02 | 0.557 | 1.47e-01 |
| POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation | 9 | 4.40e-03 | 0.548 | 3.33e-02 |
| Adrenoceptors | 9 | 4.43e-03 | 0.548 | 3.34e-02 |
| Vasopressin-like receptors | 5 | 3.46e-02 | 0.546 | 1.59e-01 |
| Kidney development | 45 | 2.62e-10 | 0.544 | 2.52e-08 |
| CREB3 factors activate genes | 8 | 8.62e-03 | -0.536 | 5.65e-02 |
| Alpha-oxidation of phytanate | 6 | 2.32e-02 | -0.535 | 1.20e-01 |
| Dopamine receptors | 5 | 4.03e-02 | 0.530 | 1.74e-01 |
| Nephron development | 13 | 1.15e-03 | 0.521 | 1.24e-02 |
| Neurotransmitter clearance | 9 | 8.57e-03 | 0.506 | 5.65e-02 |
| Erythropoietin activates STAT5 | 7 | 2.19e-02 | 0.500 | 1.14e-01 |
| Metal sequestration by antimicrobial proteins | 5 | 5.41e-02 | -0.497 | 2.16e-01 |
| Vitamins | 6 | 3.52e-02 | 0.497 | 1.61e-01 |
| Negative regulation of activity of TFAP2 (AP-2) family transcription factors | 10 | 7.59e-03 | 0.487 | 5.12e-02 |
| Prednisone ADME | 9 | 1.24e-02 | 0.481 | 7.27e-02 |
| Signaling by RNF43 mutants | 8 | 1.96e-02 | 0.476 | 1.06e-01 |
| Recycling of eIF2:GDP | 7 | 2.93e-02 | -0.476 | 1.42e-01 |
| Sensing of DNA Double Strand Breaks | 6 | 4.48e-02 | -0.473 | 1.87e-01 |
| Organic anion transport | 5 | 6.93e-02 | -0.469 | 2.55e-01 |
| Ligand-receptor interactions | 8 | 2.37e-02 | 0.462 | 1.22e-01 |
| Defective F9 activation | 5 | 7.82e-02 | 0.455 | 2.77e-01 |
| Establishment of Sister Chromatid Cohesion | 9 | 1.93e-02 | -0.450 | 1.05e-01 |
| Activation of TRKA receptors | 6 | 5.80e-02 | 0.447 | 2.25e-01 |
| Calcitonin-like ligand receptors | 10 | 1.50e-02 | 0.444 | 8.59e-02 |
| Folding of actin by CCT/TriC | 10 | 1.57e-02 | -0.441 | 8.82e-02 |
| RUNX1 regulates transcription of genes involved in WNT signaling | 5 | 8.92e-02 | 0.439 | 3.02e-01 |
| Tandem pore domain potassium channels | 12 | 1.01e-02 | 0.429 | 6.31e-02 |
| CD22 mediated BCR regulation | 5 | 9.81e-02 | 0.427 | 3.20e-01 |
| Mitotic Telophase/Cytokinesis | 11 | 1.58e-02 | -0.420 | 8.82e-02 |
| Phosphorylation of Emi1 | 6 | 7.61e-02 | -0.418 | 2.72e-01 |
| SRP-dependent cotranslational protein targeting to membrane | 105 | 1.29e-13 | -0.418 | 2.58e-11 |
| Formation of the nephric duct | 17 | 3.07e-03 | 0.415 | 2.60e-02 |
| Cellular response to mitochondrial stress | 8 | 4.24e-02 | -0.414 | 1.80e-01 |
| Formation of xylulose-5-phosphate | 5 | 1.09e-01 | -0.414 | 3.43e-01 |
| Cohesin Loading onto Chromatin | 8 | 4.44e-02 | -0.410 | 1.87e-01 |
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Regulation of gene expression in endocrine-committed (NEUROG3+) progenitor cells | 5 | 1.76e-03 | 8.08e-01 | 1.71e-02 |
| Regulation of gene expression in early pancreatic precursor cells | 8 | 1.42e-04 | 7.77e-01 | 2.93e-03 |
| Formation of lateral plate mesoderm | 5 | 3.27e-03 | 7.60e-01 | 2.70e-02 |
| Free fatty acid receptors | 5 | 4.13e-03 | 7.40e-01 | 3.18e-02 |
| Formation of intermediate mesoderm | 8 | 1.73e-03 | 6.39e-01 | 1.69e-02 |
| Formation of the ureteric bud | 21 | 5.43e-07 | 6.31e-01 | 1.96e-05 |
| Thyroxine biosynthesis | 10 | 5.98e-04 | 6.27e-01 | 8.25e-03 |
| Transcriptional regulation of testis differentiation | 12 | 2.05e-04 | 6.19e-01 | 3.97e-03 |
| Acrosome Reaction and Sperm:Oocyte Membrane Binding | 6 | 1.17e-02 | -5.94e-01 | 7.01e-02 |
| Electric Transmission Across Gap Junctions | 5 | 2.16e-02 | 5.93e-01 | 1.14e-01 |
| Transmission across Electrical Synapses | 5 | 2.16e-02 | 5.93e-01 | 1.14e-01 |
| Defective LFNG causes SCDO3 | 5 | 2.46e-02 | 5.80e-01 | 1.25e-01 |
| Formation of the anterior neural plate | 10 | 1.79e-03 | 5.70e-01 | 1.71e-02 |
| Cobalamin (Cbl) metabolism | 7 | 9.39e-03 | -5.67e-01 | 6.02e-02 |
| Specification of the neural plate border | 16 | 9.64e-05 | 5.63e-01 | 2.10e-03 |
| Hyaluronan biosynthesis and export | 5 | 3.10e-02 | 5.57e-01 | 1.47e-01 |
| POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation | 9 | 4.40e-03 | 5.48e-01 | 3.33e-02 |
| Adrenoceptors | 9 | 4.43e-03 | 5.48e-01 | 3.34e-02 |
| Vasopressin-like receptors | 5 | 3.46e-02 | 5.46e-01 | 1.59e-01 |
| Kidney development | 45 | 2.62e-10 | 5.44e-01 | 2.52e-08 |
| CREB3 factors activate genes | 8 | 8.62e-03 | -5.36e-01 | 5.65e-02 |
| Alpha-oxidation of phytanate | 6 | 2.32e-02 | -5.35e-01 | 1.20e-01 |
| Dopamine receptors | 5 | 4.03e-02 | 5.30e-01 | 1.74e-01 |
| Nephron development | 13 | 1.15e-03 | 5.21e-01 | 1.24e-02 |
| Neurotransmitter clearance | 9 | 8.57e-03 | 5.06e-01 | 5.65e-02 |
| Erythropoietin activates STAT5 | 7 | 2.19e-02 | 5.00e-01 | 1.14e-01 |
| Metal sequestration by antimicrobial proteins | 5 | 5.41e-02 | -4.97e-01 | 2.16e-01 |
| Vitamins | 6 | 3.52e-02 | 4.97e-01 | 1.61e-01 |
| Negative regulation of activity of TFAP2 (AP-2) family transcription factors | 10 | 7.59e-03 | 4.87e-01 | 5.12e-02 |
| Prednisone ADME | 9 | 1.24e-02 | 4.81e-01 | 7.27e-02 |
| Signaling by RNF43 mutants | 8 | 1.96e-02 | 4.76e-01 | 1.06e-01 |
| Recycling of eIF2:GDP | 7 | 2.93e-02 | -4.76e-01 | 1.42e-01 |
| Sensing of DNA Double Strand Breaks | 6 | 4.48e-02 | -4.73e-01 | 1.87e-01 |
| Organic anion transport | 5 | 6.93e-02 | -4.69e-01 | 2.55e-01 |
| Ligand-receptor interactions | 8 | 2.37e-02 | 4.62e-01 | 1.22e-01 |
| Defective F9 activation | 5 | 7.82e-02 | 4.55e-01 | 2.77e-01 |
| Establishment of Sister Chromatid Cohesion | 9 | 1.93e-02 | -4.50e-01 | 1.05e-01 |
| Activation of TRKA receptors | 6 | 5.80e-02 | 4.47e-01 | 2.25e-01 |
| Calcitonin-like ligand receptors | 10 | 1.50e-02 | 4.44e-01 | 8.59e-02 |
| Folding of actin by CCT/TriC | 10 | 1.57e-02 | -4.41e-01 | 8.82e-02 |
| RUNX1 regulates transcription of genes involved in WNT signaling | 5 | 8.92e-02 | 4.39e-01 | 3.02e-01 |
| Tandem pore domain potassium channels | 12 | 1.01e-02 | 4.29e-01 | 6.31e-02 |
| CD22 mediated BCR regulation | 5 | 9.81e-02 | 4.27e-01 | 3.20e-01 |
| Mitotic Telophase/Cytokinesis | 11 | 1.58e-02 | -4.20e-01 | 8.82e-02 |
| Phosphorylation of Emi1 | 6 | 7.61e-02 | -4.18e-01 | 2.72e-01 |
| SRP-dependent cotranslational protein targeting to membrane | 105 | 1.29e-13 | -4.18e-01 | 2.58e-11 |
| Formation of the nephric duct | 17 | 3.07e-03 | 4.15e-01 | 2.60e-02 |
| Cellular response to mitochondrial stress | 8 | 4.24e-02 | -4.14e-01 | 1.80e-01 |
| Formation of xylulose-5-phosphate | 5 | 1.09e-01 | -4.14e-01 | 3.43e-01 |
| Cohesin Loading onto Chromatin | 8 | 4.44e-02 | -4.10e-01 | 1.87e-01 |
| HDL clearance | 5 | 1.12e-01 | 4.10e-01 | 3.46e-01 |
| Regulation of gene expression in beta cells | 21 | 1.22e-03 | 4.08e-01 | 1.29e-02 |
| Activation of caspases through apoptosome-mediated cleavage | 5 | 1.15e-01 | -4.07e-01 | 3.51e-01 |
| Terminal pathway of complement | 8 | 4.75e-02 | -4.05e-01 | 1.97e-01 |
| Sema4D mediated inhibition of cell attachment and migration | 8 | 4.82e-02 | -4.03e-01 | 1.99e-01 |
| Formation of the posterior neural plate | 10 | 2.75e-02 | 4.03e-01 | 1.34e-01 |
| Serotonin receptors | 11 | 2.16e-02 | 4.00e-01 | 1.14e-01 |
| FGFR3 mutant receptor activation | 11 | 2.18e-02 | 3.99e-01 | 1.14e-01 |
| Signaling by activated point mutants of FGFR3 | 11 | 2.18e-02 | 3.99e-01 | 1.14e-01 |
| Activation of C3 and C5 | 6 | 9.23e-02 | 3.97e-01 | 3.08e-01 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | 7 | 6.96e-02 | -3.96e-01 | 2.55e-01 |
| SARS-CoV-1 modulates host translation machinery | 33 | 8.22e-05 | -3.96e-01 | 1.81e-03 |
| Eukaryotic Translation Termination | 86 | 2.32e-10 | -3.95e-01 | 2.44e-08 |
| G2/M DNA replication checkpoint | 5 | 1.27e-01 | -3.94e-01 | 3.77e-01 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 17 | 5.13e-03 | -3.92e-01 | 3.70e-02 |
| Regulation of beta-cell development | 41 | 1.53e-05 | 3.90e-01 | 4.37e-04 |
| Activation of the TFAP2 (AP-2) family of transcription factors | 11 | 2.53e-02 | 3.90e-01 | 1.27e-01 |
| Erythropoietin activates Phospholipase C gamma (PLCG) | 7 | 7.44e-02 | 3.89e-01 | 2.68e-01 |
| PINK1-PRKN Mediated Mitophagy | 21 | 2.00e-03 | -3.89e-01 | 1.86e-02 |
| Amine ligand-binding receptors | 40 | 2.03e-05 | 3.89e-01 | 5.42e-04 |
| Phase 4 - resting membrane potential | 19 | 3.33e-03 | 3.89e-01 | 2.73e-02 |
| Viral mRNA Translation | 83 | 9.29e-10 | -3.89e-01 | 7.64e-08 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 17 | 5.55e-03 | -3.88e-01 | 3.94e-02 |
| Phospholipase C-mediated cascade; FGFR3 | 12 | 2.01e-02 | 3.88e-01 | 1.08e-01 |
| Condensation of Prometaphase Chromosomes | 11 | 2.74e-02 | -3.84e-01 | 1.34e-01 |
| POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | 10 | 3.59e-02 | 3.83e-01 | 1.63e-01 |
| Voltage gated Potassium channels | 42 | 1.91e-05 | 3.81e-01 | 5.23e-04 |
| Polo-like kinase mediated events | 16 | 8.63e-03 | -3.79e-01 | 5.65e-02 |
| NGF-independant TRKA activation | 5 | 1.42e-01 | 3.79e-01 | 3.99e-01 |
| Pre-NOTCH Processing in the Endoplasmic Reticulum | 6 | 1.10e-01 | 3.77e-01 | 3.45e-01 |
| Signaling by MAPK mutants | 6 | 1.11e-01 | -3.76e-01 | 3.46e-01 |
| IkBA variant leads to EDA-ID | 6 | 1.12e-01 | -3.75e-01 | 3.46e-01 |
| AMPK inhibits chREBP transcriptional activation activity | 8 | 6.63e-02 | 3.75e-01 | 2.47e-01 |
| Peptide chain elongation | 83 | 4.06e-09 | -3.73e-01 | 2.90e-07 |
| SMAC (DIABLO) binds to IAPs | 6 | 1.14e-01 | -3.72e-01 | 3.50e-01 |
| SMAC(DIABLO)-mediated dissociation of IAP:caspase complexes | 6 | 1.14e-01 | -3.72e-01 | 3.50e-01 |
| SMAC, XIAP-regulated apoptotic response | 6 | 1.14e-01 | -3.72e-01 | 3.50e-01 |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | 12 | 2.57e-02 | 3.72e-01 | 1.28e-01 |
| Transcriptional regulation of pluripotent stem cells | 28 | 6.64e-04 | 3.72e-01 | 8.68e-03 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 88 | 2.04e-09 | -3.70e-01 | 1.57e-07 |
| Selenocysteine synthesis | 86 | 3.94e-09 | -3.67e-01 | 2.90e-07 |
| Regulation of TP53 Activity through Association with Co-factors | 14 | 1.76e-02 | 3.66e-01 | 9.73e-02 |
| RUNX1 regulates expression of components of tight junctions | 5 | 1.57e-01 | 3.65e-01 | 4.27e-01 |
| Hydrolysis of LPC | 9 | 5.82e-02 | -3.65e-01 | 2.25e-01 |
| Transport of Ribonucleoproteins into the Host Nucleus | 32 | 4.00e-04 | -3.62e-01 | 6.44e-03 |
| Nuclear Pore Complex (NPC) Disassembly | 36 | 1.75e-04 | -3.61e-01 | 3.47e-03 |
| NEP/NS2 Interacts with the Cellular Export Machinery | 32 | 4.30e-04 | -3.60e-01 | 6.67e-03 |
| p38MAPK events | 13 | 2.49e-02 | -3.59e-01 | 1.26e-01 |
| Influenza Viral RNA Transcription and Replication | 130 | 1.46e-12 | -3.59e-01 | 2.43e-10 |
| Negative regulation of TCF-dependent signaling by WNT ligand antagonists | 15 | 1.61e-02 | 3.59e-01 | 8.98e-02 |
| Eukaryotic Translation Elongation | 87 | 7.45e-09 | -3.58e-01 | 4.52e-07 |
| Formation of axial mesoderm | 14 | 2.03e-02 | 3.58e-01 | 1.09e-01 |
| Melanin biosynthesis | 5 | 1.68e-01 | 3.56e-01 | 4.44e-01 |
| Rev-mediated nuclear export of HIV RNA | 35 | 2.73e-04 | -3.55e-01 | 4.91e-03 |
| Choline catabolism | 6 | 1.32e-01 | 3.55e-01 | 3.82e-01 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 32 | 5.44e-04 | -3.53e-01 | 7.83e-03 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 32 | 5.44e-04 | -3.53e-01 | 7.83e-03 |
| Vitamin C (ascorbate) metabolism | 8 | 8.51e-02 | -3.52e-01 | 2.91e-01 |
| Synthesis of Ketone Bodies | 8 | 8.63e-02 | 3.50e-01 | 2.95e-01 |
| Interactions of Rev with host cellular proteins | 37 | 2.32e-04 | -3.50e-01 | 4.37e-03 |
| Export of Viral Ribonucleoproteins from Nucleus | 33 | 5.19e-04 | -3.49e-01 | 7.65e-03 |
| Metabolism of amine-derived hormones | 17 | 1.32e-02 | 3.47e-01 | 7.64e-02 |
| Tachykinin receptors bind tachykinins | 5 | 1.80e-01 | 3.46e-01 | 4.66e-01 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 12 | 3.80e-02 | 3.46e-01 | 1.68e-01 |
| SUMOylation of SUMOylation proteins | 35 | 3.98e-04 | -3.46e-01 | 6.44e-03 |
| Nuclear import of Rev protein | 34 | 4.84e-04 | -3.46e-01 | 7.39e-03 |
| Expression and translocation of olfactory receptors | 317 | 7.20e-26 | 3.43e-01 | 1.44e-22 |
| Cation-coupled Chloride cotransporters | 7 | 1.16e-01 | 3.43e-01 | 3.54e-01 |
| GLI proteins bind promoters of Hh responsive genes to promote transcription | 7 | 1.17e-01 | 3.42e-01 | 3.56e-01 |
| Formation of ATP by chemiosmotic coupling | 16 | 1.85e-02 | -3.40e-01 | 1.02e-01 |
| Regulation of CDH11 mRNA translation by microRNAs | 11 | 5.09e-02 | 3.40e-01 | 2.07e-01 |
| Creatine metabolism | 8 | 9.69e-02 | 3.39e-01 | 3.19e-01 |
| Maturation of hRSV A proteins | 13 | 3.46e-02 | -3.38e-01 | 1.59e-01 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 94 | 1.47e-08 | -3.38e-01 | 8.41e-07 |
| HS-GAG biosynthesis | 28 | 2.15e-03 | 3.35e-01 | 1.96e-02 |
| Vpr-mediated nuclear import of PICs | 34 | 7.37e-04 | -3.34e-01 | 9.38e-03 |
| Nuclear Envelope Breakdown | 52 | 3.12e-05 | -3.34e-01 | 7.90e-04 |
| Ficolins bind to repetitive carbohydrate structures on the target cell surface | 5 | 1.96e-01 | -3.34e-01 | 4.90e-01 |
| Formation of a pool of free 40S subunits | 93 | 3.01e-08 | -3.32e-01 | 1.47e-06 |
| RUNX1 regulates estrogen receptor mediated transcription | 6 | 1.59e-01 | 3.32e-01 | 4.31e-01 |
| Olfactory Signaling Pathway | 324 | 8.72e-25 | 3.32e-01 | 8.72e-22 |
| FGFR2c ligand binding and activation | 12 | 4.66e-02 | 3.32e-01 | 1.94e-01 |
| Influenza Infection | 149 | 2.71e-12 | -3.32e-01 | 4.17e-10 |
| RUNX2 regulates chondrocyte maturation | 5 | 2.00e-01 | 3.31e-01 | 4.92e-01 |
| Transport of the SLBP Dependant Mature mRNA | 36 | 6.10e-04 | -3.30e-01 | 8.34e-03 |
| Transport of the SLBP independent Mature mRNA | 35 | 7.35e-04 | -3.30e-01 | 9.38e-03 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 107 | 4.56e-09 | -3.28e-01 | 2.95e-07 |
| Nonsense-Mediated Decay (NMD) | 107 | 4.56e-09 | -3.28e-01 | 2.95e-07 |
| RHO GTPases activate KTN1 | 11 | 5.97e-02 | -3.28e-01 | 2.30e-01 |
| Abacavir ADME | 9 | 8.88e-02 | 3.28e-01 | 3.02e-01 |
| Triglyceride biosynthesis | 11 | 6.03e-02 | -3.27e-01 | 2.31e-01 |
| Mitophagy | 27 | 3.28e-03 | -3.27e-01 | 2.70e-02 |
| PI3K events in ERBB4 signaling | 10 | 7.46e-02 | 3.26e-01 | 2.69e-01 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 16 | 2.42e-02 | -3.25e-01 | 1.24e-01 |
| Passive transport by Aquaporins | 13 | 4.26e-02 | -3.25e-01 | 1.81e-01 |
| Respiratory electron transport | 90 | 1.11e-07 | -3.24e-01 | 4.63e-06 |
| Cap-dependent Translation Initiation | 110 | 4.72e-09 | -3.23e-01 | 2.95e-07 |
| Eukaryotic Translation Initiation | 110 | 4.72e-09 | -3.23e-01 | 2.95e-07 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 103 | 1.47e-08 | -3.23e-01 | 8.41e-07 |
| Hyaluronan uptake and degradation | 12 | 5.32e-02 | -3.22e-01 | 2.15e-01 |
| ERBB2 Activates PTK6 Signaling | 13 | 4.46e-02 | 3.22e-01 | 1.87e-01 |
| RIP-mediated NFkB activation via ZBP1 | 16 | 2.59e-02 | -3.22e-01 | 1.28e-01 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 102 | 2.11e-08 | -3.21e-01 | 1.11e-06 |
| Purine ribonucleoside monophosphate biosynthesis | 9 | 9.57e-02 | -3.21e-01 | 3.16e-01 |
| HDR through MMEJ (alt-NHEJ) | 12 | 5.54e-02 | -3.19e-01 | 2.19e-01 |
| Cross-presentation of particulate exogenous antigens (phagosomes) | 6 | 1.76e-01 | -3.19e-01 | 4.60e-01 |
| Viral Messenger RNA Synthesis | 44 | 2.53e-04 | -3.19e-01 | 4.64e-03 |
| Interactions of Vpr with host cellular proteins | 35 | 1.10e-03 | -3.19e-01 | 1.22e-02 |
| mRNA decay by 3’ to 5’ exoribonuclease | 16 | 2.75e-02 | -3.18e-01 | 1.34e-01 |
| Classical antibody-mediated complement activation | 6 | 1.78e-01 | -3.17e-01 | 4.64e-01 |
| SARS-CoV-2 modulates host translation machinery | 45 | 2.29e-04 | -3.17e-01 | 4.36e-03 |
| Regulation of CDH11 gene transcription | 10 | 8.24e-02 | 3.17e-01 | 2.87e-01 |
| CREB phosphorylation | 6 | 1.79e-01 | -3.17e-01 | 4.64e-01 |
| Cardiogenesis | 26 | 5.15e-03 | 3.17e-01 | 3.70e-02 |
| Creation of C4 and C2 activators | 14 | 4.02e-02 | -3.17e-01 | 1.74e-01 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | 16 | 2.84e-02 | -3.16e-01 | 1.38e-01 |
| Lectin pathway of complement activation | 8 | 1.22e-01 | -3.16e-01 | 3.66e-01 |
| Abacavir transmembrane transport | 5 | 2.23e-01 | 3.15e-01 | 5.24e-01 |
| FGFRL1 modulation of FGFR1 signaling | 13 | 5.00e-02 | 3.14e-01 | 2.05e-01 |
| Synthesis of GDP-mannose | 5 | 2.24e-01 | -3.14e-01 | 5.25e-01 |
| PI-3K cascade:FGFR3 | 17 | 2.55e-02 | 3.13e-01 | 1.28e-01 |
| Regulation of NPAS4 mRNA translation | 9 | 1.04e-01 | 3.13e-01 | 3.33e-01 |
| Release of apoptotic factors from the mitochondria | 6 | 1.88e-01 | -3.10e-01 | 4.78e-01 |
| Release of Hh-Np from the secreting cell | 8 | 1.29e-01 | 3.10e-01 | 3.80e-01 |
| FGFR3 ligand binding and activation | 12 | 6.38e-02 | 3.09e-01 | 2.42e-01 |
| FGFR3c ligand binding and activation | 12 | 6.38e-02 | 3.09e-01 | 2.42e-01 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | 43 | 4.92e-04 | -3.07e-01 | 7.45e-03 |
| Transport of Mature mRNA Derived from an Intronless Transcript | 42 | 5.92e-04 | -3.06e-01 | 8.22e-03 |
| Defective factor IX causes hemophilia B | 7 | 1.61e-01 | 3.06e-01 | 4.35e-01 |
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 111 | 2.56e-08 | -3.06e-01 | 1.31e-06 |
| Depolymerization of the Nuclear Lamina | 14 | 4.85e-02 | -3.04e-01 | 2.00e-01 |
| KSRP (KHSRP) binds and destabilizes mRNA | 17 | 3.03e-02 | -3.04e-01 | 1.45e-01 |
| Erythrocytes take up oxygen and release carbon dioxide | 8 | 1.39e-01 | -3.02e-01 | 3.95e-01 |
| Crosslinking of collagen fibrils | 16 | 3.70e-02 | 3.01e-01 | 1.65e-01 |
| Activation of Matrix Metalloproteinases | 30 | 4.35e-03 | 3.01e-01 | 3.31e-02 |
| Activated point mutants of FGFR2 | 16 | 3.75e-02 | 3.00e-01 | 1.66e-01 |
| Biosynthesis of maresin-like SPMs | 6 | 2.03e-01 | 3.00e-01 | 4.95e-01 |
| Sulfide oxidation to sulfate | 5 | 2.46e-01 | 3.00e-01 | 5.50e-01 |
| Synthesis of PIPs at the ER membrane | 5 | 2.46e-01 | -2.99e-01 | 5.50e-01 |
| Translation | 277 | 1.14e-17 | -2.99e-01 | 3.81e-15 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 69 | 1.83e-05 | -2.98e-01 | 5.08e-04 |
| Phospholipase C-mediated cascade; FGFR2 | 17 | 3.34e-02 | 2.98e-01 | 1.56e-01 |
| NFE2L2 regulating inflammation associated genes | 5 | 2.49e-01 | 2.98e-01 | 5.53e-01 |
| Physiological factors | 14 | 5.41e-02 | 2.97e-01 | 2.16e-01 |
| RHOBTB3 ATPase cycle | 8 | 1.46e-01 | 2.97e-01 | 4.08e-01 |
| Transcription of E2F targets under negative control by DREAM complex | 19 | 2.55e-02 | -2.96e-01 | 1.28e-01 |
| Class C/3 (Metabotropic glutamate/pheromone receptors) | 38 | 1.61e-03 | 2.96e-01 | 1.61e-02 |
| Defective factor VIII causes hemophilia A | 5 | 2.52e-01 | -2.96e-01 | 5.56e-01 |
| Regulation of HMOX1 expression and activity | 5 | 2.53e-01 | -2.95e-01 | 5.56e-01 |
| p75NTR negatively regulates cell cycle via SC1 | 6 | 2.13e-01 | 2.94e-01 | 5.10e-01 |
| ERKs are inactivated | 13 | 6.77e-02 | -2.93e-01 | 2.51e-01 |
| Activated NTRK2 signals through PI3K | 7 | 1.80e-01 | 2.92e-01 | 4.67e-01 |
| FGFR4 ligand binding and activation | 13 | 6.93e-02 | 2.91e-01 | 2.55e-01 |
| ZBP1(DAI) mediated induction of type I IFNs | 20 | 2.43e-02 | -2.91e-01 | 1.24e-01 |
| Postmitotic nuclear pore complex (NPC) reformation | 27 | 8.95e-03 | -2.91e-01 | 5.76e-02 |
| ERK/MAPK targets | 20 | 2.46e-02 | -2.90e-01 | 1.25e-01 |
| RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | 6 | 2.19e-01 | 2.90e-01 | 5.18e-01 |
| Urea cycle | 9 | 1.33e-01 | -2.89e-01 | 3.84e-01 |
| Formation of annular gap junctions | 11 | 9.69e-02 | -2.89e-01 | 3.19e-01 |
| Activation of the AP-1 family of transcription factors | 10 | 1.14e-01 | -2.89e-01 | 3.49e-01 |
| Phospholipase C-mediated cascade; FGFR4 | 14 | 6.14e-02 | 2.89e-01 | 2.35e-01 |
| Transport of Mature Transcript to Cytoplasm | 78 | 1.09e-05 | -2.88e-01 | 3.19e-04 |
| Diseases associated with visual transduction | 11 | 9.83e-02 | 2.88e-01 | 3.20e-01 |
| Diseases of the neuronal system | 11 | 9.83e-02 | 2.88e-01 | 3.20e-01 |
| Retinoid cycle disease events | 11 | 9.83e-02 | 2.88e-01 | 3.20e-01 |
| SARS-CoV-2 modulates autophagy | 11 | 9.84e-02 | -2.88e-01 | 3.20e-01 |
| Vitamin B5 (pantothenate) metabolism | 19 | 3.00e-02 | -2.88e-01 | 1.44e-01 |
| MAP2K and MAPK activation | 38 | 2.19e-03 | -2.87e-01 | 1.98e-02 |
| NS1 Mediated Effects on Host Pathways | 41 | 1.48e-03 | -2.87e-01 | 1.49e-02 |
| Endosomal/Vacuolar pathway | 10 | 1.17e-01 | 2.86e-01 | 3.56e-01 |
| Synthesis of wybutosine at G37 of tRNA(Phe) | 6 | 2.25e-01 | -2.86e-01 | 5.25e-01 |
| Lysosphingolipid and LPA receptors | 14 | 6.44e-02 | 2.85e-01 | 2.43e-01 |
| Cross-presentation of soluble exogenous antigens (endosomes) | 46 | 8.23e-04 | -2.85e-01 | 9.92e-03 |
| IRF3 mediated activation of type 1 IFN | 5 | 2.70e-01 | -2.85e-01 | 5.74e-01 |
| Phospholipase C-mediated cascade: FGFR1 | 16 | 4.91e-02 | 2.84e-01 | 2.01e-01 |
| ChREBP activates metabolic gene expression | 8 | 1.64e-01 | 2.84e-01 | 4.41e-01 |
| Signalling to p38 via RIT and RIN | 5 | 2.72e-01 | 2.83e-01 | 5.75e-01 |
| SUMOylation of DNA replication proteins | 46 | 8.81e-04 | -2.83e-01 | 1.04e-02 |
| Citric acid cycle (TCA cycle) | 21 | 2.46e-02 | -2.83e-01 | 1.25e-01 |
| Resolution of D-Loop Structures | 33 | 4.89e-03 | -2.83e-01 | 3.58e-02 |
| Formation of the ternary complex, and subsequently, the 43S complex | 45 | 1.04e-03 | -2.83e-01 | 1.17e-02 |
| Mitochondrial translation elongation | 87 | 5.19e-06 | -2.83e-01 | 1.65e-04 |
| Protein hydroxylation | 17 | 4.40e-02 | -2.82e-01 | 1.86e-01 |
| Mitochondrial translation | 93 | 2.56e-06 | -2.82e-01 | 8.68e-05 |
| Complex I biogenesis | 49 | 6.40e-04 | -2.82e-01 | 8.64e-03 |
| Post-transcriptional silencing by small RNAs | 7 | 1.97e-01 | 2.82e-01 | 4.90e-01 |
| Mitochondrial translation initiation | 87 | 5.67e-06 | -2.81e-01 | 1.77e-04 |
| CaMK IV-mediated phosphorylation of CREB | 10 | 1.25e-01 | -2.80e-01 | 3.73e-01 |
| G0 and Early G1 | 27 | 1.17e-02 | -2.80e-01 | 7.01e-02 |
| Regulation of ornithine decarboxylase (ODC) | 50 | 6.14e-04 | -2.80e-01 | 8.34e-03 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 42 | 1.80e-03 | -2.78e-01 | 1.71e-02 |
| Signaling by RAS mutants | 42 | 1.80e-03 | -2.78e-01 | 1.71e-02 |
| Signaling by moderate kinase activity BRAF mutants | 42 | 1.80e-03 | -2.78e-01 | 1.71e-02 |
| Signaling downstream of RAS mutants | 42 | 1.80e-03 | -2.78e-01 | 1.71e-02 |
| Defects in cobalamin (B12) metabolism | 13 | 8.31e-02 | -2.78e-01 | 2.88e-01 |
| Vitamin B1 (thiamin) metabolism | 5 | 2.84e-01 | -2.77e-01 | 5.84e-01 |
| Vpu mediated degradation of CD4 | 51 | 6.45e-04 | -2.76e-01 | 8.66e-03 |
| Metabolism of non-coding RNA | 52 | 5.73e-04 | -2.76e-01 | 8.06e-03 |
| snRNP Assembly | 52 | 5.73e-04 | -2.76e-01 | 8.06e-03 |
| Mitochondrial translation termination | 87 | 8.73e-06 | -2.76e-01 | 2.64e-04 |
| Calcineurin activates NFAT | 9 | 1.53e-01 | -2.75e-01 | 4.19e-01 |
| RA biosynthesis pathway | 22 | 2.56e-02 | 2.75e-01 | 1.28e-01 |
| MAPK targets/ Nuclear events mediated by MAP kinases | 29 | 1.05e-02 | -2.74e-01 | 6.51e-02 |
| Metabolism of polyamines | 56 | 3.81e-04 | -2.74e-01 | 6.40e-03 |
| Signaling by FGFR3 in disease | 21 | 3.02e-02 | 2.73e-01 | 1.45e-01 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | 32 | 7.60e-03 | -2.73e-01 | 5.12e-02 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 33 | 6.72e-03 | -2.73e-01 | 4.60e-02 |
| rRNA processing in the nucleus and cytosol | 181 | 2.65e-10 | -2.72e-01 | 2.52e-08 |
| Diseases associated with N-glycosylation of proteins | 19 | 4.00e-02 | -2.72e-01 | 1.74e-01 |
| Coenzyme A biosynthesis | 7 | 2.13e-01 | -2.72e-01 | 5.10e-01 |
| Autodegradation of the E3 ubiquitin ligase COP1 | 50 | 8.97e-04 | -2.71e-01 | 1.05e-02 |
| Signaling by high-kinase activity BRAF mutants | 34 | 6.20e-03 | -2.71e-01 | 4.29e-02 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 51 | 8.24e-04 | -2.71e-01 | 9.92e-03 |
| Negative regulation of NOTCH4 signaling | 53 | 6.59e-04 | -2.70e-01 | 8.68e-03 |
| Major pathway of rRNA processing in the nucleolus and cytosol | 172 | 9.56e-10 | -2.70e-01 | 7.64e-08 |
| GPCR ligand binding | 443 | 1.88e-22 | 2.70e-01 | 9.40e-20 |
| Orexin and neuropeptides FF and QRFP bind to their respective receptors | 8 | 1.87e-01 | 2.69e-01 | 4.78e-01 |
| Dectin-1 mediated noncanonical NF-kB signaling | 61 | 2.92e-04 | -2.68e-01 | 5.12e-03 |
| Class A/1 (Rhodopsin-like receptors) | 312 | 3.68e-16 | 2.68e-01 | 1.05e-13 |
| TNFR1-mediated ceramide production | 6 | 2.56e-01 | -2.68e-01 | 5.58e-01 |
| Ciprofloxacin ADME | 5 | 3.00e-01 | 2.68e-01 | 6.00e-01 |
| SCF-beta-TrCP mediated degradation of Emi1 | 54 | 6.62e-04 | -2.68e-01 | 8.68e-03 |
| Sema4D induced cell migration and growth-cone collapse | 20 | 3.82e-02 | -2.68e-01 | 1.68e-01 |
| RAF-independent MAPK1/3 activation | 22 | 2.99e-02 | -2.67e-01 | 1.44e-01 |
| Sensory perception of salty taste | 6 | 2.57e-01 | 2.67e-01 | 5.60e-01 |
| Translation initiation complex formation | 52 | 8.55e-04 | -2.67e-01 | 1.02e-02 |
| Eicosanoids | 12 | 1.09e-01 | -2.67e-01 | 3.43e-01 |
| Synthesis of pyrophosphates in the cytosol | 8 | 1.91e-01 | 2.67e-01 | 4.82e-01 |
| Fibronectin matrix formation | 6 | 2.58e-01 | -2.67e-01 | 5.60e-01 |
| Peptide ligand-binding receptors | 187 | 3.16e-10 | 2.67e-01 | 2.88e-08 |
| Type I hemidesmosome assembly | 11 | 1.26e-01 | -2.67e-01 | 3.75e-01 |
| Fructose metabolism | 7 | 2.22e-01 | -2.66e-01 | 5.24e-01 |
| p130Cas linkage to MAPK signaling for integrins | 15 | 7.43e-02 | -2.66e-01 | 2.68e-01 |
| Defective binding of VWF variant to GPIb:IX:V | 7 | 2.23e-01 | 2.66e-01 | 5.24e-01 |
| Enhanced binding of GP1BA variant to VWF multimer:collagen | 7 | 2.23e-01 | 2.66e-01 | 5.24e-01 |
| Selenoamino acid metabolism | 109 | 1.74e-06 | -2.65e-01 | 6.00e-05 |
| Potassium Channels | 102 | 3.83e-06 | 2.65e-01 | 1.24e-04 |
| Telomere C-strand synthesis initiation | 12 | 1.12e-01 | -2.65e-01 | 3.46e-01 |
| Regulation of commissural axon pathfinding by SLIT and ROBO | 10 | 1.48e-01 | 2.65e-01 | 4.10e-01 |
| Initiation of Nuclear Envelope (NE) Reformation | 18 | 5.24e-02 | -2.64e-01 | 2.12e-01 |
| Intestinal absorption | 5 | 3.07e-01 | 2.64e-01 | 6.07e-01 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 49 | 1.39e-03 | -2.64e-01 | 1.44e-02 |
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 51 | 1.12e-03 | -2.64e-01 | 1.22e-02 |
| p53-Independent DNA Damage Response | 51 | 1.12e-03 | -2.64e-01 | 1.22e-02 |
| p53-Independent G1/S DNA damage checkpoint | 51 | 1.12e-03 | -2.64e-01 | 1.22e-02 |
| mRNA Splicing - Minor Pathway | 52 | 1.01e-03 | -2.64e-01 | 1.16e-02 |
| GRB2 events in ERBB2 signaling | 16 | 6.81e-02 | 2.63e-01 | 2.52e-01 |
| Ribosomal scanning and start codon recognition | 52 | 1.02e-03 | -2.63e-01 | 1.16e-02 |
| O-glycosylation of TSR domain-containing proteins | 38 | 5.09e-03 | 2.63e-01 | 3.69e-02 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 54 | 8.48e-04 | -2.62e-01 | 1.02e-02 |
| rRNA processing | 190 | 4.55e-10 | -2.62e-01 | 3.96e-08 |
| FRS-mediated FGFR3 signaling | 19 | 4.81e-02 | 2.62e-01 | 1.99e-01 |
| PI3K events in ERBB2 signaling | 16 | 6.98e-02 | 2.62e-01 | 2.55e-01 |
| Autodegradation of Cdh1 by Cdh1:APC/C | 63 | 3.38e-04 | -2.61e-01 | 5.79e-03 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 13 | 1.04e-01 | -2.61e-01 | 3.33e-01 |
| PI-3K cascade:FGFR2 | 22 | 3.44e-02 | 2.61e-01 | 1.58e-01 |
| Negative regulation of MAPK pathway | 41 | 3.92e-03 | -2.60e-01 | 3.09e-02 |
| SCF(Skp2)-mediated degradation of p27/p21 | 59 | 5.44e-04 | -2.60e-01 | 7.83e-03 |
| DNA Damage Reversal | 8 | 2.03e-01 | 2.60e-01 | 4.95e-01 |
| EPHB-mediated forward signaling | 41 | 3.99e-03 | -2.60e-01 | 3.11e-02 |
| SUMO is conjugated to E1 (UBA2:SAE1) | 5 | 3.15e-01 | -2.60e-01 | 6.16e-01 |
| SHC-mediated cascade:FGFR3 | 17 | 6.43e-02 | 2.59e-01 | 2.42e-01 |
| Signaling by RAF1 mutants | 39 | 5.10e-03 | -2.59e-01 | 3.69e-02 |
| TRAF6 mediated NF-kB activation | 24 | 2.80e-02 | -2.59e-01 | 1.36e-01 |
| RNA Polymerase III Chain Elongation | 18 | 5.70e-02 | -2.59e-01 | 2.22e-01 |
| PI3K Cascade | 43 | 3.35e-03 | 2.59e-01 | 2.73e-02 |
| Linoleic acid (LA) metabolism | 7 | 2.36e-01 | 2.59e-01 | 5.42e-01 |
| Na+/Cl- dependent neurotransmitter transporters | 18 | 5.80e-02 | 2.58e-01 | 2.25e-01 |
| Receptor-type tyrosine-protein phosphatases | 16 | 7.42e-02 | 2.58e-01 | 2.68e-01 |
| IRS-related events triggered by IGF1R | 50 | 1.64e-03 | 2.57e-01 | 1.63e-02 |
| Regulation of innate immune responses to cytosolic DNA | 15 | 8.43e-02 | -2.57e-01 | 2.90e-01 |
| Ubiquitin-dependent degradation of Cyclin D | 51 | 1.48e-03 | -2.57e-01 | 1.49e-02 |
| XBP1(S) activates chaperone genes | 43 | 3.52e-03 | -2.57e-01 | 2.83e-02 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 73 | 1.47e-04 | -2.57e-01 | 2.98e-03 |
| SUMOylation of ubiquitinylation proteins | 39 | 5.61e-03 | -2.56e-01 | 3.94e-02 |
| CDH11 homotypic and heterotypic interactions | 7 | 2.41e-01 | 2.56e-01 | 5.46e-01 |
| CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde | 8 | 2.10e-01 | -2.56e-01 | 5.07e-01 |
| Degradation of GLI2 by the proteasome | 59 | 6.73e-04 | -2.56e-01 | 8.74e-03 |
| Impaired BRCA2 binding to RAD51 | 35 | 8.93e-03 | -2.55e-01 | 5.76e-02 |
| NIK–>noncanonical NF-kB signaling | 58 | 7.70e-04 | -2.55e-01 | 9.54e-03 |
| AURKA Activation by TPX2 | 69 | 2.52e-04 | -2.55e-01 | 4.64e-03 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 53 | 1.38e-03 | -2.54e-01 | 1.43e-02 |
| Regulation of expression of SLITs and ROBOs | 161 | 2.72e-08 | -2.54e-01 | 1.36e-06 |
| DNA replication initiation | 7 | 2.45e-01 | -2.54e-01 | 5.50e-01 |
| Class B/2 (Secretin family receptors) | 93 | 2.41e-05 | 2.53e-01 | 6.34e-04 |
| APC/C:Cdc20 mediated degradation of Securin | 67 | 3.39e-04 | -2.53e-01 | 5.79e-03 |
| Fructose catabolism | 5 | 3.27e-01 | -2.53e-01 | 6.29e-01 |
| IRE1alpha activates chaperones | 45 | 3.47e-03 | -2.52e-01 | 2.81e-02 |
| Scavenging of heme from plasma | 12 | 1.32e-01 | -2.51e-01 | 3.83e-01 |
| IGF1R signaling cascade | 51 | 1.95e-03 | 2.51e-01 | 1.82e-02 |
| Cellular response to starvation | 145 | 1.92e-07 | -2.50e-01 | 7.68e-06 |
| Attachment and Entry 9694614 | 16 | 8.36e-02 | 2.50e-01 | 2.89e-01 |
| Vif-mediated degradation of APOBEC3G | 53 | 1.66e-03 | -2.50e-01 | 1.63e-02 |
| Sema4D in semaphorin signaling | 24 | 3.42e-02 | -2.50e-01 | 1.58e-01 |
| FGFR3b ligand binding and activation | 7 | 2.53e-01 | 2.50e-01 | 5.56e-01 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 72 | 2.56e-04 | -2.49e-01 | 4.65e-03 |
| Defective B3GALTL causes PpS | 37 | 8.79e-03 | 2.49e-01 | 5.71e-02 |
| PI-3K cascade:FGFR1 | 21 | 4.89e-02 | 2.48e-01 | 2.01e-01 |
| Specification of primordial germ cells | 11 | 1.54e-01 | 2.48e-01 | 4.23e-01 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 14 | 1.08e-01 | -2.48e-01 | 3.42e-01 |
| PI-3K cascade:FGFR4 | 19 | 6.14e-02 | 2.48e-01 | 2.35e-01 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 24 | 3.56e-02 | -2.48e-01 | 1.62e-01 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | 88 | 6.04e-05 | -2.47e-01 | 1.39e-03 |
| Diseases of Mismatch Repair (MMR) | 5 | 3.39e-01 | -2.47e-01 | 6.44e-01 |
| Activation of NF-kappaB in B cells | 65 | 5.69e-04 | -2.47e-01 | 8.06e-03 |
| Presynaptic phase of homologous DNA pairing and strand exchange | 40 | 6.96e-03 | -2.47e-01 | 4.73e-02 |
| Regulation of PTEN mRNA translation | 24 | 3.65e-02 | 2.47e-01 | 1.64e-01 |
| The citric acid (TCA) cycle and respiratory electron transport | 159 | 8.58e-08 | -2.46e-01 | 3.65e-06 |
| FGFR1 ligand binding and activation | 17 | 7.92e-02 | 2.46e-01 | 2.78e-01 |
| WNT ligand biogenesis and trafficking | 25 | 3.34e-02 | 2.46e-01 | 1.56e-01 |
| Defective CFTR causes cystic fibrosis | 60 | 1.02e-03 | -2.45e-01 | 1.16e-02 |
| Trafficking and processing of endosomal TLR | 11 | 1.60e-01 | 2.45e-01 | 4.32e-01 |
| Downstream signaling events of B Cell Receptor (BCR) | 79 | 1.69e-04 | -2.45e-01 | 3.38e-03 |
| Anchoring of the basal body to the plasma membrane | 93 | 4.55e-05 | -2.45e-01 | 1.11e-03 |
| GLI3 is processed to GLI3R by the proteasome | 59 | 1.16e-03 | -2.45e-01 | 1.24e-02 |
| Sensory perception of taste | 45 | 4.54e-03 | 2.45e-01 | 3.40e-02 |
| Formyl peptide receptors bind formyl peptides and many other ligands | 8 | 2.31e-01 | 2.44e-01 | 5.34e-01 |
| Formation of definitive endoderm | 16 | 9.11e-02 | 2.44e-01 | 3.06e-01 |
| Aryl hydrocarbon receptor signalling | 7 | 2.64e-01 | -2.44e-01 | 5.65e-01 |
| DEx/H-box helicases activate type I IFN and inflammatory cytokines production | 7 | 2.65e-01 | -2.43e-01 | 5.66e-01 |
| Degradation of GLI1 by the proteasome | 59 | 1.24e-03 | -2.43e-01 | 1.30e-02 |
| Regulation of CDH11 Expression and Function | 29 | 2.37e-02 | 2.43e-01 | 1.22e-01 |
| Epithelial-Mesenchymal Transition (EMT) during gastrulation | 7 | 2.67e-01 | 2.43e-01 | 5.67e-01 |
| Hh mutants are degraded by ERAD | 55 | 1.92e-03 | -2.42e-01 | 1.81e-02 |
| MASTL Facilitates Mitotic Progression | 10 | 1.86e-01 | -2.41e-01 | 4.78e-01 |
| Regulation of FZD by ubiquitination | 21 | 5.62e-02 | 2.41e-01 | 2.20e-01 |
| Negative regulators of DDX58/IFIH1 signaling | 34 | 1.52e-02 | -2.41e-01 | 8.69e-02 |
| Phosphorylation of the APC/C | 20 | 6.28e-02 | -2.40e-01 | 2.39e-01 |
| HDR through Homologous Recombination (HRR) | 66 | 7.63e-04 | -2.40e-01 | 9.54e-03 |
| Loss of Nlp from mitotic centrosomes | 66 | 7.73e-04 | -2.39e-01 | 9.54e-03 |
| Loss of proteins required for interphase microtubule organization from the centrosome | 66 | 7.73e-04 | -2.39e-01 | 9.54e-03 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 73 | 4.29e-04 | -2.38e-01 | 6.67e-03 |
| Unfolded Protein Response (UPR) | 86 | 1.37e-04 | -2.38e-01 | 2.86e-03 |
| VLDL clearance | 6 | 3.13e-01 | 2.38e-01 | 6.15e-01 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 54 | 2.53e-03 | -2.38e-01 | 2.23e-02 |
| NR1H2 & NR1H3 regulate gene expression to limit cholesterol uptake | 5 | 3.58e-01 | -2.37e-01 | 6.66e-01 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 15 | 1.11e-01 | 2.37e-01 | 3.46e-01 |
| IRS-mediated signalling | 47 | 4.91e-03 | 2.37e-01 | 3.58e-02 |
| Class I peroxisomal membrane protein import | 19 | 7.35e-02 | -2.37e-01 | 2.67e-01 |
| Zinc efflux and compartmentalization by the SLC30 family | 5 | 3.59e-01 | -2.37e-01 | 6.66e-01 |
| Processing of Capped Intron-Containing Pre-mRNA | 265 | 3.07e-11 | -2.37e-01 | 4.10e-09 |
| Sensory perception of sweet, bitter, and umami (glutamate) taste | 40 | 9.61e-03 | 2.37e-01 | 6.10e-02 |
| The activation of arylsulfatases | 8 | 2.47e-01 | -2.36e-01 | 5.50e-01 |
| Ketone body metabolism | 9 | 2.19e-01 | 2.36e-01 | 5.18e-01 |
| CDK-mediated phosphorylation and removal of Cdc6 | 72 | 5.20e-04 | -2.36e-01 | 7.65e-03 |
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 41 | 8.80e-03 | -2.36e-01 | 5.71e-02 |
| Diseases of DNA Double-Strand Break Repair | 41 | 8.80e-03 | -2.36e-01 | 5.71e-02 |
| Cyclin E associated events during G1/S transition | 82 | 2.15e-04 | -2.36e-01 | 4.13e-03 |
| Peptide hormone biosynthesis | 11 | 1.75e-01 | 2.36e-01 | 4.60e-01 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 52 | 3.25e-03 | 2.36e-01 | 2.70e-02 |
| Downstream signaling of activated FGFR1 | 31 | 2.31e-02 | 2.36e-01 | 1.19e-01 |
| Defective GALNT3 causes HFTC | 18 | 8.36e-02 | -2.36e-01 | 2.89e-01 |
| Phosphate bond hydrolysis by NUDT proteins | 7 | 2.81e-01 | -2.36e-01 | 5.82e-01 |
| Josephin domain DUBs | 10 | 1.97e-01 | -2.35e-01 | 4.90e-01 |
| SHC1 events in ERBB4 signaling | 14 | 1.27e-01 | 2.35e-01 | 3.77e-01 |
| MET interacts with TNS proteins | 5 | 3.62e-01 | -2.35e-01 | 6.67e-01 |
| Regulation of APC/C activators between G1/S and early anaphase | 80 | 2.81e-04 | -2.35e-01 | 5.02e-03 |
| Interleukin-20 family signaling | 24 | 4.64e-02 | 2.35e-01 | 1.93e-01 |
| Regulation of Apoptosis | 52 | 3.45e-03 | -2.34e-01 | 2.80e-02 |
| Regulation of RUNX3 expression and activity | 54 | 2.88e-03 | -2.34e-01 | 2.45e-02 |
| SUMOylation of RNA binding proteins | 47 | 5.49e-03 | -2.34e-01 | 3.92e-02 |
| Interleukin-9 signaling | 7 | 2.84e-01 | 2.34e-01 | 5.84e-01 |
| Inflammasomes | 21 | 6.36e-02 | -2.34e-01 | 2.42e-01 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 76 | 4.30e-04 | -2.34e-01 | 6.67e-03 |
| Downstream signaling of activated FGFR3 | 24 | 4.77e-02 | 2.33e-01 | 1.98e-01 |
| Acetylcholine Neurotransmitter Release Cycle | 17 | 9.57e-02 | 2.33e-01 | 3.16e-01 |
| tRNA processing in the nucleus | 58 | 2.14e-03 | -2.33e-01 | 1.96e-02 |
| Homologous DNA Pairing and Strand Exchange | 43 | 8.30e-03 | -2.33e-01 | 5.53e-02 |
| Surfactant metabolism | 26 | 4.01e-02 | 2.33e-01 | 1.74e-01 |
| Platelet Adhesion to exposed collagen | 16 | 1.07e-01 | 2.32e-01 | 3.40e-01 |
| SARS-CoV-1-host interactions | 91 | 1.28e-04 | -2.32e-01 | 2.70e-03 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 27 | 3.69e-02 | -2.32e-01 | 1.65e-01 |
| Biosynthesis of EPA-derived SPMs | 6 | 3.25e-01 | 2.32e-01 | 6.27e-01 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 12 | 1.65e-01 | -2.32e-01 | 4.41e-01 |
| Role of ABL in ROBO-SLIT signaling | 8 | 2.58e-01 | 2.31e-01 | 5.60e-01 |
| Cyclin A:Cdk2-associated events at S phase entry | 84 | 2.52e-04 | -2.31e-01 | 4.64e-03 |
| TFAP2 (AP-2) family regulates transcription of cell cycle factors | 5 | 3.72e-01 | 2.31e-01 | 6.77e-01 |
| Nef Mediated CD8 Down-regulation | 7 | 2.92e-01 | 2.30e-01 | 5.92e-01 |
| The NLRP3 inflammasome | 16 | 1.11e-01 | -2.30e-01 | 3.46e-01 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | 75 | 5.79e-04 | -2.30e-01 | 8.09e-03 |
| Nicotinamide salvaging | 19 | 8.39e-02 | 2.29e-01 | 2.89e-01 |
| Biosynthesis of maresins | 8 | 2.62e-01 | 2.29e-01 | 5.65e-01 |
| HDR through Single Strand Annealing (SSA) | 37 | 1.61e-02 | -2.29e-01 | 8.97e-02 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | 15 | 1.25e-01 | -2.29e-01 | 3.74e-01 |
| RNA polymerase II transcribes snRNA genes | 74 | 6.94e-04 | -2.28e-01 | 8.95e-03 |
| Early Phase of HIV Life Cycle | 14 | 1.41e-01 | -2.27e-01 | 3.97e-01 |
| Centrosome maturation | 78 | 5.16e-04 | -2.27e-01 | 7.65e-03 |
| Recruitment of mitotic centrosome proteins and complexes | 78 | 5.16e-04 | -2.27e-01 | 7.65e-03 |
| Fatty acids | 14 | 1.41e-01 | -2.27e-01 | 3.97e-01 |
| Sensory Perception | 526 | 4.65e-19 | 2.27e-01 | 1.86e-16 |
| Lewis blood group biosynthesis | 18 | 9.52e-02 | 2.27e-01 | 3.16e-01 |
| Impaired BRCA2 binding to PALB2 | 24 | 5.43e-02 | -2.27e-01 | 2.16e-01 |
| VEGF binds to VEGFR leading to receptor dimerization | 7 | 2.99e-01 | 2.27e-01 | 5.99e-01 |
| VEGF ligand-receptor interactions | 7 | 2.99e-01 | 2.27e-01 | 5.99e-01 |
| Regulation of PLK1 Activity at G2/M Transition | 84 | 3.34e-04 | -2.26e-01 | 5.79e-03 |
| Stabilization of p53 | 55 | 3.70e-03 | -2.26e-01 | 2.96e-02 |
| Intrinsic Pathway of Fibrin Clot Formation | 21 | 7.29e-02 | 2.26e-01 | 2.65e-01 |
| Trafficking of GluR2-containing AMPA receptors | 15 | 1.30e-01 | 2.26e-01 | 3.81e-01 |
| RHO GTPases Activate ROCKs | 19 | 8.93e-02 | -2.25e-01 | 3.02e-01 |
| mRNA Splicing | 200 | 4.14e-08 | -2.25e-01 | 1.88e-06 |
| FRS-mediated FGFR2 signaling | 24 | 5.69e-02 | 2.25e-01 | 2.22e-01 |
| Peroxisomal lipid metabolism | 28 | 3.99e-02 | -2.24e-01 | 1.74e-01 |
| BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members | 9 | 2.46e-01 | -2.23e-01 | 5.50e-01 |
| Metabolism of ingested SeMet, Sec, MeSec into H2Se | 8 | 2.76e-01 | 2.22e-01 | 5.77e-01 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 28 | 4.18e-02 | -2.22e-01 | 1.79e-01 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | 25 | 5.45e-02 | -2.22e-01 | 2.16e-01 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | 25 | 5.45e-02 | -2.22e-01 | 2.16e-01 |
| Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 25 | 5.45e-02 | -2.22e-01 | 2.16e-01 |
| Defective homologous recombination repair (HRR) due to PALB2 loss of function | 25 | 5.45e-02 | -2.22e-01 | 2.16e-01 |
| Degradation of DVL | 56 | 4.02e-03 | -2.22e-01 | 3.13e-02 |
| Heparan sulfate/heparin (HS-GAG) metabolism | 52 | 5.60e-03 | 2.22e-01 | 3.94e-02 |
| CLEC7A/inflammasome pathway | 6 | 3.46e-01 | -2.22e-01 | 6.53e-01 |
| mRNA Splicing - Major Pathway | 190 | 1.31e-07 | -2.22e-01 | 5.36e-06 |
| Metabolism of RNA | 689 | 4.75e-23 | -2.21e-01 | 3.16e-20 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | 14 | 1.53e-01 | 2.20e-01 | 4.21e-01 |
| Germ layer formation at gastrulation | 16 | 1.27e-01 | 2.20e-01 | 3.77e-01 |
| rRNA modification in the nucleus and cytosol | 57 | 4.13e-03 | -2.20e-01 | 3.18e-02 |
| Mitotic Prophase | 104 | 1.09e-04 | -2.20e-01 | 2.34e-03 |
| APC/C-mediated degradation of cell cycle proteins | 87 | 4.03e-04 | -2.19e-01 | 6.44e-03 |
| Regulation of mitotic cell cycle | 87 | 4.03e-04 | -2.19e-01 | 6.44e-03 |
| RNA Polymerase III Transcription Termination | 23 | 6.88e-02 | -2.19e-01 | 2.54e-01 |
| SHC-mediated cascade:FGFR2 | 22 | 7.52e-02 | 2.19e-01 | 2.70e-01 |
| Diseases of DNA repair | 51 | 6.85e-03 | -2.19e-01 | 4.68e-02 |
| Butyrophilin (BTN) family interactions | 12 | 1.90e-01 | 2.18e-01 | 4.81e-01 |
| Cristae formation | 26 | 5.41e-02 | -2.18e-01 | 2.16e-01 |
| Apoptotic factor-mediated response | 18 | 1.09e-01 | -2.18e-01 | 3.43e-01 |
| Prefoldin mediated transfer of substrate to CCT/TriC | 26 | 5.47e-02 | -2.18e-01 | 2.17e-01 |
| Receptor Mediated Mitophagy | 10 | 2.35e-01 | -2.17e-01 | 5.41e-01 |
| Gap junction degradation | 12 | 1.94e-01 | -2.16e-01 | 4.88e-01 |
| Rap1 signalling | 16 | 1.35e-01 | -2.16e-01 | 3.86e-01 |
| Glycolysis | 72 | 1.55e-03 | -2.16e-01 | 1.56e-02 |
| Separation of Sister Chromatids | 182 | 5.22e-07 | -2.16e-01 | 1.93e-05 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 91 | 3.92e-04 | -2.15e-01 | 6.44e-03 |
| Amplification of signal from the kinetochores | 91 | 3.92e-04 | -2.15e-01 | 6.44e-03 |
| Regulation of PTEN localization | 8 | 2.92e-01 | -2.15e-01 | 5.93e-01 |
| Mitotic Prometaphase | 192 | 2.91e-07 | -2.15e-01 | 1.12e-05 |
| Regulation of RAS by GAPs | 66 | 2.58e-03 | -2.14e-01 | 2.26e-02 |
| Fanconi Anemia Pathway | 34 | 3.05e-02 | -2.14e-01 | 1.45e-01 |
| Interleukin-12 signaling | 41 | 1.78e-02 | -2.14e-01 | 9.80e-02 |
| Synaptic adhesion-like molecules | 19 | 1.07e-01 | 2.14e-01 | 3.38e-01 |
| PI5P Regulates TP53 Acetylation | 8 | 2.97e-01 | -2.13e-01 | 5.97e-01 |
| Mitotic Metaphase and Anaphase | 226 | 3.37e-08 | -2.13e-01 | 1.60e-06 |
| Mitotic Anaphase | 225 | 3.62e-08 | -2.13e-01 | 1.68e-06 |
| Host Interactions of HIV factors | 126 | 3.63e-05 | -2.13e-01 | 8.99e-04 |
| Acyl chain remodeling of CL | 5 | 4.11e-01 | -2.12e-01 | 7.09e-01 |
| G1/S Transition | 127 | 3.64e-05 | -2.12e-01 | 8.99e-04 |
| Mitotic Spindle Checkpoint | 108 | 1.43e-04 | -2.12e-01 | 2.93e-03 |
| M Phase | 366 | 3.44e-12 | -2.12e-01 | 4.91e-10 |
| FRS-mediated FGFR1 signaling | 23 | 7.88e-02 | 2.12e-01 | 2.78e-01 |
| Metabolism of folate and pterines | 17 | 1.32e-01 | -2.11e-01 | 3.82e-01 |
| Norepinephrine Neurotransmitter Release Cycle | 17 | 1.33e-01 | 2.11e-01 | 3.84e-01 |
| Transcriptional regulation by small RNAs | 70 | 2.34e-03 | -2.10e-01 | 2.08e-02 |
| G1/S DNA Damage Checkpoints | 66 | 3.20e-03 | -2.10e-01 | 2.68e-02 |
| Integrin signaling | 27 | 5.99e-02 | -2.09e-01 | 2.31e-01 |
| p53-Dependent G1 DNA Damage Response | 64 | 3.88e-03 | -2.09e-01 | 3.07e-02 |
| p53-Dependent G1/S DNA damage checkpoint | 64 | 3.88e-03 | -2.09e-01 | 3.07e-02 |
| Displacement of DNA glycosylase by APEX1 | 9 | 2.79e-01 | -2.09e-01 | 5.79e-01 |
| FRS-mediated FGFR4 signaling | 21 | 9.91e-02 | 2.08e-01 | 3.22e-01 |
| Regulation of Expression and Function of Type II Classical Cadherins | 32 | 4.20e-02 | 2.08e-01 | 1.79e-01 |
| Regulation of Homotypic Cell-Cell Adhesion | 32 | 4.20e-02 | 2.08e-01 | 1.79e-01 |
| Downstream signaling of activated FGFR2 | 29 | 5.31e-02 | 2.07e-01 | 2.15e-01 |
| Interleukin-12 family signaling | 51 | 1.06e-02 | -2.07e-01 | 6.52e-02 |
| EGFR interacts with phospholipase C-gamma | 8 | 3.11e-01 | 2.07e-01 | 6.13e-01 |
| Resolution of Sister Chromatid Cohesion | 118 | 1.10e-04 | -2.06e-01 | 2.34e-03 |
| Frs2-mediated activation | 12 | 2.18e-01 | -2.05e-01 | 5.18e-01 |
| Glucose metabolism | 92 | 6.62e-04 | -2.05e-01 | 8.68e-03 |
| SHC-mediated cascade:FGFR1 | 21 | 1.04e-01 | 2.05e-01 | 3.33e-01 |
| InlA-mediated entry of Listeria monocytogenes into host cells | 9 | 2.87e-01 | -2.05e-01 | 5.88e-01 |
| Defective GALNT12 causes CRCS1 | 18 | 1.34e-01 | -2.04e-01 | 3.86e-01 |
| Hormone ligand-binding receptors | 13 | 2.03e-01 | 2.04e-01 | 4.95e-01 |
| AKT phosphorylates targets in the cytosol | 14 | 1.87e-01 | -2.04e-01 | 4.78e-01 |
| ISG15 antiviral mechanism | 74 | 2.47e-03 | -2.04e-01 | 2.18e-02 |
| Methionine salvage pathway | 6 | 3.88e-01 | -2.03e-01 | 6.89e-01 |
| RHO GTPases Activate Formins | 134 | 4.99e-05 | -2.03e-01 | 1.18e-03 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | 76 | 2.33e-03 | -2.02e-01 | 2.08e-02 |
| mRNA 3’-end processing | 53 | 1.10e-02 | -2.02e-01 | 6.73e-02 |
| CASP8 activity is inhibited | 11 | 2.47e-01 | -2.02e-01 | 5.50e-01 |
| Dimerization of procaspase-8 | 11 | 2.47e-01 | -2.02e-01 | 5.50e-01 |
| Regulation by c-FLIP | 11 | 2.47e-01 | -2.02e-01 | 5.50e-01 |
| Synthesis of PG | 8 | 3.24e-01 | -2.01e-01 | 6.26e-01 |
| GABA receptor activation | 57 | 8.54e-03 | 2.01e-01 | 5.65e-02 |
| Defective C1GALT1C1 causes TNPS | 18 | 1.39e-01 | -2.01e-01 | 3.96e-01 |
| UCH proteinases | 93 | 7.93e-04 | -2.01e-01 | 9.72e-03 |
| mRNA decay by 5’ to 3’ exoribonuclease | 15 | 1.78e-01 | -2.01e-01 | 4.64e-01 |
| NR1H2 and NR1H3-mediated signaling | 53 | 1.14e-02 | 2.01e-01 | 6.94e-02 |
| Regulation of CDH11 function | 10 | 2.72e-01 | 2.01e-01 | 5.75e-01 |
| Hh mutants abrogate ligand secretion | 58 | 8.26e-03 | -2.00e-01 | 5.52e-02 |
| SARS-CoV-1 activates/modulates innate immune responses | 39 | 3.03e-02 | -2.00e-01 | 1.45e-01 |
| Mitotic G1 phase and G1/S transition | 145 | 3.12e-05 | -2.00e-01 | 7.90e-04 |
| RHO GTPases Activate WASPs and WAVEs | 34 | 4.34e-02 | -2.00e-01 | 1.84e-01 |
| SHC-mediated cascade:FGFR4 | 19 | 1.32e-01 | 2.00e-01 | 3.82e-01 |
| Signaling by ROBO receptors | 206 | 7.70e-07 | -2.00e-01 | 2.70e-05 |
| FGFR2 alternative splicing | 26 | 7.83e-02 | -1.99e-01 | 2.77e-01 |
| Inhibition of Signaling by Overexpressed EGFR | 7 | 3.61e-01 | 1.99e-01 | 6.67e-01 |
| Signaling by Overexpressed Wild-Type EGFR in Cancer | 7 | 3.61e-01 | 1.99e-01 | 6.67e-01 |
| Switching of origins to a post-replicative state | 91 | 1.01e-03 | -1.99e-01 | 1.16e-02 |
| Degradation of AXIN | 54 | 1.13e-02 | -1.99e-01 | 6.88e-02 |
| Signaling by activated point mutants of FGFR1 | 11 | 2.53e-01 | 1.99e-01 | 5.56e-01 |
| Nucleotide biosynthesis | 12 | 2.34e-01 | -1.98e-01 | 5.39e-01 |
| Propionyl-CoA catabolism | 5 | 4.43e-01 | -1.98e-01 | 7.36e-01 |
| Uptake of dietary cobalamins into enterocytes | 9 | 3.03e-01 | 1.98e-01 | 6.03e-01 |
| Insulin receptor signalling cascade | 53 | 1.29e-02 | 1.97e-01 | 7.50e-02 |
| NR1H2 & NR1H3 regulate gene expression linked to lipogenesis | 9 | 3.06e-01 | 1.97e-01 | 6.07e-01 |
| Wax and plasmalogen biosynthesis | 5 | 4.46e-01 | -1.97e-01 | 7.38e-01 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | 21 | 1.19e-01 | -1.97e-01 | 3.59e-01 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 21 | 1.19e-01 | -1.97e-01 | 3.59e-01 |
| Orc1 removal from chromatin | 70 | 4.44e-03 | -1.97e-01 | 3.34e-02 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 53 | 1.33e-02 | -1.97e-01 | 7.69e-02 |
| Formation of apoptosome | 10 | 2.82e-01 | -1.97e-01 | 5.82e-01 |
| Regulation of the apoptosome activity | 10 | 2.82e-01 | -1.97e-01 | 5.82e-01 |
| Cytochrome c-mediated apoptotic response | 12 | 2.39e-01 | -1.96e-01 | 5.45e-01 |
| Cell-extracellular matrix interactions | 16 | 1.74e-01 | -1.96e-01 | 4.58e-01 |
| Cytoprotection by HMOX1 | 58 | 9.80e-03 | -1.96e-01 | 6.20e-02 |
| GDP-fucose biosynthesis | 6 | 4.06e-01 | 1.96e-01 | 7.05e-01 |
| WNT mediated activation of DVL | 8 | 3.37e-01 | -1.96e-01 | 6.43e-01 |
| Mitotic G2-G2/M phases | 193 | 2.82e-06 | -1.95e-01 | 9.40e-05 |
| RAF activation | 32 | 5.57e-02 | -1.95e-01 | 2.19e-01 |
| Cell Cycle Checkpoints | 264 | 4.56e-08 | -1.95e-01 | 2.03e-06 |
| G2/M Checkpoints | 144 | 5.25e-05 | -1.95e-01 | 1.22e-03 |
| NOTCH4 Intracellular Domain Regulates Transcription | 19 | 1.42e-01 | 1.95e-01 | 3.99e-01 |
| Mineralocorticoid biosynthesis | 5 | 4.51e-01 | 1.95e-01 | 7.40e-01 |
| mitochondrial fatty acid beta-oxidation of unsaturated fatty acids | 6 | 4.09e-01 | -1.94e-01 | 7.07e-01 |
| G2/M Transition | 191 | 3.72e-06 | -1.94e-01 | 1.22e-04 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | 5 | 4.52e-01 | -1.94e-01 | 7.41e-01 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 20 | 1.34e-01 | -1.94e-01 | 3.86e-01 |
| Erythrocytes take up carbon dioxide and release oxygen | 12 | 2.46e-01 | -1.94e-01 | 5.50e-01 |
| O2/CO2 exchange in erythrocytes | 12 | 2.46e-01 | -1.94e-01 | 5.50e-01 |
| ABC transporter disorders | 76 | 3.65e-03 | -1.93e-01 | 2.93e-02 |
| SHC-related events triggered by IGF1R | 9 | 3.17e-01 | 1.93e-01 | 6.20e-01 |
| ERBB2 Regulates Cell Motility | 15 | 1.97e-01 | 1.92e-01 | 4.90e-01 |
| Nicotinate metabolism | 31 | 6.41e-02 | 1.92e-01 | 2.42e-01 |
| Downstream signaling of activated FGFR4 | 26 | 9.01e-02 | 1.92e-01 | 3.03e-01 |
| Activated NTRK2 signals through FRS2 and FRS3 | 11 | 2.71e-01 | 1.92e-01 | 5.74e-01 |
| Signaling by BRAF and RAF1 fusions | 63 | 8.62e-03 | -1.91e-01 | 5.65e-02 |
| Ribavirin ADME | 11 | 2.72e-01 | -1.91e-01 | 5.75e-01 |
| Opsins | 7 | 3.82e-01 | 1.91e-01 | 6.85e-01 |
| Blood group systems biosynthesis | 21 | 1.30e-01 | 1.91e-01 | 3.81e-01 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | 21 | 1.30e-01 | -1.91e-01 | 3.81e-01 |
| Cyclin A/B1/B2 associated events during G2/M transition | 24 | 1.06e-01 | -1.91e-01 | 3.38e-01 |
| RNA Polymerase II Transcription Termination | 62 | 9.46e-03 | -1.91e-01 | 6.04e-02 |
| MAP kinase activation | 58 | 1.24e-02 | -1.90e-01 | 7.27e-02 |
| Negative feedback regulation of MAPK pathway | 6 | 4.23e-01 | -1.89e-01 | 7.18e-01 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | 10 | 3.01e-01 | -1.89e-01 | 6.01e-01 |
| Mitochondrial biogenesis | 84 | 2.82e-03 | -1.88e-01 | 2.41e-02 |
| CLEC7A (Dectin-1) signaling | 97 | 1.34e-03 | -1.88e-01 | 1.39e-02 |
| DNA Replication Pre-Initiation | 120 | 3.69e-04 | -1.88e-01 | 6.25e-03 |
| G alpha (i) signalling events | 304 | 1.69e-08 | 1.88e-01 | 9.16e-07 |
| Transcriptional Regulation by MECP2 | 60 | 1.18e-02 | 1.88e-01 | 7.04e-02 |
| Post-translational protein phosphorylation | 100 | 1.18e-03 | 1.88e-01 | 1.26e-02 |
| Transcriptional activation of mitochondrial biogenesis | 50 | 2.17e-02 | -1.88e-01 | 1.14e-01 |
| Axonal growth inhibition (RHOA activation) | 8 | 3.58e-01 | -1.88e-01 | 6.66e-01 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 43 | 3.34e-02 | 1.87e-01 | 1.56e-01 |
| Assembly of the pre-replicative complex | 105 | 9.04e-04 | -1.87e-01 | 1.05e-02 |
| Activation of RAC1 | 12 | 2.61e-01 | 1.87e-01 | 5.65e-01 |
| Glycoprotein hormones | 9 | 3.33e-01 | 1.86e-01 | 6.37e-01 |
| Cell Cycle, Mitotic | 507 | 7.68e-13 | -1.86e-01 | 1.40e-10 |
| FCERI mediated NF-kB activation | 78 | 4.57e-03 | -1.86e-01 | 3.41e-02 |
| Mitochondrial protein import | 57 | 1.54e-02 | -1.86e-01 | 8.73e-02 |
| Downregulation of ERBB4 signaling | 9 | 3.35e-01 | -1.86e-01 | 6.40e-01 |
| Oncogenic MAPK signaling | 78 | 4.63e-03 | -1.85e-01 | 3.43e-02 |
| G1/S-Specific Transcription | 28 | 8.98e-02 | -1.85e-01 | 3.03e-01 |
| Signal transduction by L1 | 20 | 1.52e-01 | -1.85e-01 | 4.19e-01 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 11 | 2.88e-01 | -1.85e-01 | 5.89e-01 |
| tRNA processing | 105 | 1.12e-03 | -1.84e-01 | 1.22e-02 |
| Reversible hydration of carbon dioxide | 11 | 2.91e-01 | 1.84e-01 | 5.91e-01 |
| Arachidonate production from DAG | 5 | 4.77e-01 | -1.83e-01 | 7.61e-01 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 64 | 1.15e-02 | -1.83e-01 | 6.96e-02 |
| Methylation | 14 | 2.37e-01 | -1.83e-01 | 5.43e-01 |
| S Phase | 159 | 7.19e-05 | -1.82e-01 | 1.63e-03 |
| Recruitment of NuMA to mitotic centrosomes | 90 | 2.81e-03 | -1.82e-01 | 2.41e-02 |
| Heme biosynthesis | 13 | 2.56e-01 | -1.82e-01 | 5.59e-01 |
| Signaling by the B Cell Receptor (BCR) | 106 | 1.27e-03 | -1.81e-01 | 1.33e-02 |
| Interleukin-1 signaling | 110 | 1.04e-03 | -1.81e-01 | 1.17e-02 |
| Removal of the Flap Intermediate from the C-strand | 17 | 1.98e-01 | -1.81e-01 | 4.90e-01 |
| Chylomicron assembly | 10 | 3.24e-01 | 1.80e-01 | 6.26e-01 |
| Keratinization | 198 | 1.24e-05 | 1.80e-01 | 3.61e-04 |
| Signaling by ERBB2 TMD/JMD mutants | 22 | 1.44e-01 | 1.80e-01 | 4.02e-01 |
| Mitochondrial protein degradation | 84 | 4.34e-03 | -1.80e-01 | 3.31e-02 |
| Activation of BAD and translocation to mitochondria | 15 | 2.27e-01 | -1.80e-01 | 5.28e-01 |
| Cholesterol biosynthesis | 25 | 1.20e-01 | -1.79e-01 | 3.63e-01 |
| ER-Phagosome pathway | 86 | 4.05e-03 | -1.79e-01 | 3.14e-02 |
| Deadenylation-dependent mRNA decay | 53 | 2.42e-02 | -1.79e-01 | 1.24e-01 |
| Adherens junctions interactions | 58 | 1.87e-02 | 1.78e-01 | 1.03e-01 |
| RUNX3 regulates CDKN1A transcription | 7 | 4.14e-01 | -1.78e-01 | 7.11e-01 |
| ABC-family proteins mediated transport | 99 | 2.16e-03 | -1.78e-01 | 1.96e-02 |
| Prolonged ERK activation events | 14 | 2.49e-01 | -1.78e-01 | 5.53e-01 |
| Signaling by TGF-beta Receptor Complex in Cancer | 8 | 3.84e-01 | -1.78e-01 | 6.87e-01 |
| Reversal of alkylation damage by DNA dioxygenases | 7 | 4.16e-01 | 1.78e-01 | 7.13e-01 |
| Nuclear events mediated by NFE2L2 | 92 | 3.25e-03 | -1.78e-01 | 2.70e-02 |
| Triglyceride catabolism | 23 | 1.41e-01 | 1.77e-01 | 3.97e-01 |
| RIPK1-mediated regulated necrosis | 29 | 9.82e-02 | -1.77e-01 | 3.20e-01 |
| Regulation of necroptotic cell death | 29 | 9.82e-02 | -1.77e-01 | 3.20e-01 |
| EML4 and NUDC in mitotic spindle formation | 112 | 1.19e-03 | -1.77e-01 | 1.26e-02 |
| Signaling by ERBB2 KD Mutants | 25 | 1.27e-01 | 1.76e-01 | 3.77e-01 |
| HIV elongation arrest and recovery | 33 | 8.01e-02 | -1.76e-01 | 2.81e-01 |
| Pausing and recovery of HIV elongation | 33 | 8.01e-02 | -1.76e-01 | 2.81e-01 |
| Cell Cycle | 631 | 4.81e-14 | -1.76e-01 | 1.07e-11 |
| Anchoring fibril formation | 13 | 2.73e-01 | 1.76e-01 | 5.75e-01 |
| Deposition of new CENPA-containing nucleosomes at the centromere | 46 | 3.99e-02 | -1.75e-01 | 1.74e-01 |
| Nucleosome assembly | 46 | 3.99e-02 | -1.75e-01 | 1.74e-01 |
| Zygotic genome activation (ZGA) | 13 | 2.74e-01 | 1.75e-01 | 5.76e-01 |
| Signalling to RAS | 20 | 1.75e-01 | -1.75e-01 | 4.60e-01 |
| TNF signaling | 54 | 2.66e-02 | -1.74e-01 | 1.30e-01 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 15 | 2.43e-01 | -1.74e-01 | 5.49e-01 |
| Sensory processing of sound by outer hair cells of the cochlea | 49 | 3.49e-02 | -1.74e-01 | 1.60e-01 |
| Acyl chain remodeling of DAG and TAG | 5 | 5.00e-01 | -1.74e-01 | 7.65e-01 |
| SARS-CoV-2-host interactions | 183 | 4.90e-05 | -1.74e-01 | 1.18e-03 |
| Activation of SMO | 18 | 2.02e-01 | 1.74e-01 | 4.94e-01 |
| Signaling by GPCR | 672 | 1.49e-14 | 1.74e-01 | 3.72e-12 |
| Hedgehog ligand biogenesis | 64 | 1.62e-02 | -1.74e-01 | 8.98e-02 |
| E3 ubiquitin ligases ubiquitinate target proteins | 54 | 2.73e-02 | -1.74e-01 | 1.34e-01 |
| CHL1 interactions | 9 | 3.69e-01 | 1.73e-01 | 6.74e-01 |
| FGFR2 ligand binding and activation | 19 | 1.92e-01 | 1.73e-01 | 4.84e-01 |
| Fertilization | 26 | 1.28e-01 | -1.73e-01 | 3.77e-01 |
| Downstream TCR signaling | 89 | 4.91e-03 | -1.73e-01 | 3.58e-02 |
| Interleukin-35 Signalling | 12 | 3.01e-01 | -1.72e-01 | 6.01e-01 |
| Gap junction assembly | 35 | 7.78e-02 | 1.72e-01 | 2.76e-01 |
| Constitutive Signaling by NOTCH1 t(7;9)(NOTCH1:M1580 K2555) Translocation Mutant | 7 | 4.30e-01 | 1.72e-01 | 7.25e-01 |
| Signaling by NOTCH1 t(7;9)(NOTCH1:M1580 K2555) Translocation Mutant | 7 | 4.30e-01 | 1.72e-01 | 7.25e-01 |
| Translocation of ZAP-70 to Immunological synapse | 13 | 2.84e-01 | 1.72e-01 | 5.84e-01 |
| Regulation of TNFR1 signaling | 46 | 4.41e-02 | -1.72e-01 | 1.86e-01 |
| Incretin synthesis, secretion, and inactivation | 23 | 1.55e-01 | 1.71e-01 | 4.23e-01 |
| Activated NTRK2 signals through RAS | 9 | 3.74e-01 | 1.71e-01 | 6.79e-01 |
| Tyrosine catabolism | 5 | 5.08e-01 | -1.71e-01 | 7.70e-01 |
| GABA synthesis, release, reuptake and degradation | 19 | 2.00e-01 | 1.70e-01 | 4.92e-01 |
| Nuclear Envelope (NE) Reassembly | 73 | 1.23e-02 | -1.69e-01 | 7.27e-02 |
| Signaling by membrane-tethered fusions of PDGFRA or PDGFRB | 5 | 5.12e-01 | 1.69e-01 | 7.71e-01 |
| Lipid particle organization | 6 | 4.73e-01 | 1.69e-01 | 7.61e-01 |
| SUMO is transferred from E1 to E2 (UBE2I, UBC9) | 7 | 4.39e-01 | -1.69e-01 | 7.32e-01 |
| DNA Double-Strand Break Repair | 144 | 4.70e-04 | -1.69e-01 | 7.23e-03 |
| Cell-cell junction organization | 88 | 6.24e-03 | 1.69e-01 | 4.30e-02 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 117 | 1.65e-03 | 1.68e-01 | 1.63e-02 |
| Signalling to ERKs | 34 | 8.94e-02 | -1.68e-01 | 3.02e-01 |
| Integration of provirus | 9 | 3.82e-01 | -1.68e-01 | 6.85e-01 |
| APC-Cdc20 mediated degradation of Nek2A | 26 | 1.38e-01 | -1.68e-01 | 3.95e-01 |
| G2/M DNA damage checkpoint | 72 | 1.38e-02 | -1.68e-01 | 7.95e-02 |
| Pausing and recovery of Tat-mediated HIV elongation | 31 | 1.06e-01 | -1.68e-01 | 3.38e-01 |
| Tat-mediated HIV elongation arrest and recovery | 31 | 1.06e-01 | -1.68e-01 | 3.38e-01 |
| FasL/ CD95L signaling | 5 | 5.18e-01 | -1.67e-01 | 7.76e-01 |
| HCMV Late Events | 81 | 9.60e-03 | -1.66e-01 | 6.10e-02 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 20 | 1.98e-01 | -1.66e-01 | 4.90e-01 |
| DNA Damage Recognition in GG-NER | 36 | 8.46e-02 | -1.66e-01 | 2.90e-01 |
| TRAF3-dependent IRF activation pathway | 15 | 2.65e-01 | -1.66e-01 | 5.66e-01 |
| Protein localization | 152 | 4.19e-04 | -1.66e-01 | 6.64e-03 |
| LTC4-CYSLTR mediated IL4 production | 6 | 4.82e-01 | -1.66e-01 | 7.61e-01 |
| Constitutive Signaling by AKT1 E17K in Cancer | 25 | 1.52e-01 | -1.66e-01 | 4.19e-01 |
| Synthesis of 12-eicosatetraenoic acid derivatives | 7 | 4.49e-01 | -1.65e-01 | 7.38e-01 |
| Assembly of active LPL and LIPC lipase complexes | 18 | 2.25e-01 | -1.65e-01 | 5.25e-01 |
| RHO GTPases Activate NADPH Oxidases | 21 | 1.90e-01 | -1.65e-01 | 4.81e-01 |
| TICAM1, RIP1-mediated IKK complex recruitment | 18 | 2.26e-01 | -1.65e-01 | 5.27e-01 |
| Cargo concentration in the ER | 31 | 1.13e-01 | -1.65e-01 | 3.46e-01 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 27 | 1.40e-01 | -1.64e-01 | 3.96e-01 |
| Metabolism of cofactors | 19 | 2.16e-01 | -1.64e-01 | 5.15e-01 |
| NOTCH3 Intracellular Domain Regulates Transcription | 24 | 1.65e-01 | 1.64e-01 | 4.41e-01 |
| Synthesis of DNA | 119 | 2.03e-03 | -1.64e-01 | 1.88e-02 |
| CYP2E1 reactions | 9 | 3.98e-01 | 1.63e-01 | 6.99e-01 |
| ABC transporters in lipid homeostasis | 17 | 2.46e-01 | -1.63e-01 | 5.50e-01 |
| Loss of MECP2 binding ability to the NCoR/SMRT complex | 5 | 5.29e-01 | 1.62e-01 | 7.85e-01 |
| Nuclear signaling by ERBB4 | 32 | 1.12e-01 | 1.62e-01 | 3.46e-01 |
| Regulation of HSF1-mediated heat shock response | 79 | 1.27e-02 | -1.62e-01 | 7.45e-02 |
| RAS processing | 22 | 1.88e-01 | -1.62e-01 | 4.78e-01 |
| Attachment of GPI anchor to uPAR | 7 | 4.58e-01 | -1.62e-01 | 7.44e-01 |
| Tight junction interactions | 28 | 1.39e-01 | 1.62e-01 | 3.96e-01 |
| Assembly of collagen fibrils and other multimeric structures | 59 | 3.21e-02 | 1.61e-01 | 1.51e-01 |
| Degradation of beta-catenin by the destruction complex | 83 | 1.15e-02 | -1.61e-01 | 6.95e-02 |
| Antiviral mechanism by IFN-stimulated genes | 144 | 8.95e-04 | -1.60e-01 | 1.05e-02 |
| Acyl chain remodelling of PI | 17 | 2.53e-01 | -1.60e-01 | 5.56e-01 |
| FGFR1c ligand binding and activation | 13 | 3.17e-01 | 1.60e-01 | 6.20e-01 |
| Homology Directed Repair | 114 | 3.19e-03 | -1.60e-01 | 2.68e-02 |
| Defective Intrinsic Pathway for Apoptosis | 25 | 1.66e-01 | -1.60e-01 | 4.43e-01 |
| DSCAM interactions | 11 | 3.59e-01 | -1.60e-01 | 6.66e-01 |
| Protein ubiquitination | 72 | 1.92e-02 | -1.60e-01 | 1.05e-01 |
| Association of TriC/CCT with target proteins during biosynthesis | 38 | 8.88e-02 | -1.60e-01 | 3.02e-01 |
| Neuronal System | 389 | 6.63e-08 | 1.59e-01 | 2.88e-06 |
| SOS-mediated signalling | 7 | 4.65e-01 | 1.59e-01 | 7.52e-01 |
| DNA Replication | 148 | 8.22e-04 | -1.59e-01 | 9.92e-03 |
| Activation of ATR in response to replication stress | 37 | 9.52e-02 | -1.59e-01 | 3.16e-01 |
| SHC1 events in ERBB2 signaling | 22 | 1.98e-01 | 1.58e-01 | 4.90e-01 |
| Unblocking of NMDA receptors, glutamate binding and activation | 19 | 2.33e-01 | 1.58e-01 | 5.36e-01 |
| Somitogenesis | 54 | 4.45e-02 | -1.58e-01 | 1.87e-01 |
| GPCR downstream signalling | 602 | 3.56e-11 | 1.58e-01 | 4.45e-09 |
| Miscellaneous transport and binding events | 24 | 1.81e-01 | 1.58e-01 | 4.67e-01 |
| Removal of the Flap Intermediate | 13 | 3.26e-01 | -1.57e-01 | 6.28e-01 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 34 | 1.13e-01 | 1.57e-01 | 3.46e-01 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 36 | 1.04e-01 | -1.57e-01 | 3.33e-01 |
| NCAM1 interactions | 41 | 8.29e-02 | 1.57e-01 | 2.88e-01 |
| Interferon alpha/beta signaling | 68 | 2.60e-02 | 1.56e-01 | 1.28e-01 |
| Defects in vitamin and cofactor metabolism | 21 | 2.16e-01 | -1.56e-01 | 5.15e-01 |
| Peroxisomal protein import | 62 | 3.41e-02 | -1.56e-01 | 1.58e-01 |
| Signaling by CSF1 (M-CSF) in myeloid cells | 30 | 1.40e-01 | -1.55e-01 | 3.97e-01 |
| The canonical retinoid cycle in rods (twilight vision) | 23 | 1.97e-01 | 1.55e-01 | 4.90e-01 |
| MyD88 cascade initiated on plasma membrane | 91 | 1.05e-02 | -1.55e-01 | 6.50e-02 |
| Toll Like Receptor 10 (TLR10) Cascade | 91 | 1.05e-02 | -1.55e-01 | 6.50e-02 |
| Toll Like Receptor 5 (TLR5) Cascade | 91 | 1.05e-02 | -1.55e-01 | 6.50e-02 |
| WNT5A-dependent internalization of FZD4 | 15 | 2.98e-01 | 1.55e-01 | 5.99e-01 |
| MET activates RAS signaling | 11 | 3.73e-01 | -1.55e-01 | 6.79e-01 |
| Activation of PUMA and translocation to mitochondria | 9 | 4.21e-01 | 1.55e-01 | 7.16e-01 |
| Biosynthesis of DHA-derived SPMs | 17 | 2.71e-01 | 1.54e-01 | 5.74e-01 |
| Cytosolic sensors of pathogen-associated DNA | 63 | 3.42e-02 | -1.54e-01 | 1.58e-01 |
| Activation of RAS in B cells | 5 | 5.51e-01 | -1.54e-01 | 8.00e-01 |
| Antigen processing-Cross presentation | 97 | 8.88e-03 | -1.54e-01 | 5.74e-02 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 108 | 5.79e-03 | -1.54e-01 | 4.05e-02 |
| Metallothioneins bind metals | 11 | 3.78e-01 | 1.54e-01 | 6.83e-01 |
| MECP2 regulates neuronal receptors and channels | 17 | 2.74e-01 | 1.53e-01 | 5.76e-01 |
| C-type lectin receptors (CLRs) | 138 | 1.91e-03 | -1.53e-01 | 1.80e-02 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 95 | 1.00e-02 | -1.53e-01 | 6.31e-02 |
| Eicosanoid ligand-binding receptors | 14 | 3.23e-01 | 1.53e-01 | 6.26e-01 |
| Degradation of the extracellular matrix | 134 | 2.29e-03 | 1.53e-01 | 2.05e-02 |
| NR1H2 & NR1H3 regulate gene expression linked to gluconeogenesis | 5 | 5.55e-01 | 1.52e-01 | 8.02e-01 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 12 | 3.60e-01 | 1.52e-01 | 6.67e-01 |
| Defective EXT2 causes exostoses 2 | 12 | 3.60e-01 | 1.52e-01 | 6.67e-01 |
| SUMOylation of intracellular receptors | 29 | 1.55e-01 | 1.52e-01 | 4.24e-01 |
| Transport of organic anions | 10 | 4.05e-01 | 1.52e-01 | 7.04e-01 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 18 | 2.64e-01 | -1.52e-01 | 5.65e-01 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 31 | 1.43e-01 | -1.52e-01 | 4.02e-01 |
| Metabolism of fat-soluble vitamins | 46 | 7.48e-02 | 1.52e-01 | 2.69e-01 |
| Beta oxidation of octanoyl-CoA to hexanoyl-CoA | 5 | 5.58e-01 | -1.51e-01 | 8.04e-01 |
| Cellular response to heat stress | 96 | 1.06e-02 | -1.51e-01 | 6.52e-02 |
| Purine salvage | 12 | 3.66e-01 | -1.51e-01 | 6.71e-01 |
| Cytosolic tRNA aminoacylation | 22 | 2.22e-01 | -1.50e-01 | 5.24e-01 |
| RHO GTPase Effectors | 272 | 1.98e-05 | -1.50e-01 | 5.35e-04 |
| Suppression of phagosomal maturation | 13 | 3.48e-01 | -1.50e-01 | 6.54e-01 |
| Gastrulation | 125 | 3.76e-03 | 1.50e-01 | 3.00e-02 |
| Processing and activation of SUMO | 10 | 4.11e-01 | -1.50e-01 | 7.09e-01 |
| Signaling by BMP | 30 | 1.55e-01 | 1.50e-01 | 4.24e-01 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 12 | 3.69e-01 | 1.50e-01 | 6.74e-01 |
| alpha-linolenic acid (ALA) metabolism | 12 | 3.69e-01 | 1.50e-01 | 6.74e-01 |
| CRMPs in Sema3A signaling | 15 | 3.16e-01 | 1.50e-01 | 6.18e-01 |
| Retinoid metabolism and transport | 42 | 9.36e-02 | 1.50e-01 | 3.12e-01 |
| Synthesis of 5-eicosatetraenoic acids | 9 | 4.38e-01 | -1.49e-01 | 7.32e-01 |
| TCR signaling | 108 | 7.37e-03 | -1.49e-01 | 4.99e-02 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | 14 | 3.34e-01 | 1.49e-01 | 6.38e-01 |
| IRS activation | 5 | 5.64e-01 | 1.49e-01 | 8.08e-01 |
| activated TAK1 mediates p38 MAPK activation | 20 | 2.50e-01 | -1.49e-01 | 5.54e-01 |
| Signaling by ERBB2 in Cancer | 26 | 1.91e-01 | 1.48e-01 | 4.81e-01 |
| Translesion synthesis by POLK | 17 | 2.91e-01 | -1.48e-01 | 5.91e-01 |
| Caspase-mediated cleavage of cytoskeletal proteins | 12 | 3.76e-01 | -1.48e-01 | 6.82e-01 |
| Regulation of NPAS4 gene expression | 13 | 3.57e-01 | 1.48e-01 | 6.66e-01 |
| TYSND1 cleaves peroxisomal proteins | 7 | 4.99e-01 | -1.47e-01 | 7.65e-01 |
| Myogenesis | 29 | 1.70e-01 | 1.47e-01 | 4.48e-01 |
| HIV Life Cycle | 145 | 2.21e-03 | -1.47e-01 | 1.99e-02 |
| Pre-NOTCH Transcription and Translation | 67 | 3.73e-02 | 1.47e-01 | 1.66e-01 |
| DAP12 signaling | 27 | 1.87e-01 | -1.47e-01 | 4.78e-01 |
| Polymerase switching on the C-strand of the telomere | 25 | 2.04e-01 | -1.47e-01 | 4.95e-01 |
| Diseases of mitotic cell cycle | 37 | 1.23e-01 | -1.47e-01 | 3.69e-01 |
| Prevention of phagosomal-lysosomal fusion | 9 | 4.47e-01 | -1.46e-01 | 7.38e-01 |
| Induction of Cell-Cell Fusion | 12 | 3.80e-01 | 1.46e-01 | 6.85e-01 |
| Gene Silencing by RNA | 104 | 9.97e-03 | -1.46e-01 | 6.29e-02 |
| Regulation of PTEN stability and activity | 67 | 3.86e-02 | -1.46e-01 | 1.70e-01 |
| Synthesis of PE | 13 | 3.62e-01 | -1.46e-01 | 6.67e-01 |
| Toll Like Receptor 3 (TLR3) Cascade | 99 | 1.20e-02 | -1.46e-01 | 7.12e-02 |
| HIV Infection | 222 | 1.80e-04 | -1.46e-01 | 3.54e-03 |
| ROS and RNS production in phagocytes | 33 | 1.47e-01 | -1.46e-01 | 4.10e-01 |
| Serine biosynthesis | 9 | 4.49e-01 | 1.46e-01 | 7.39e-01 |
| Processive synthesis on the C-strand of the telomere | 19 | 2.72e-01 | -1.46e-01 | 5.75e-01 |
| Repression of WNT target genes | 14 | 3.46e-01 | 1.45e-01 | 6.53e-01 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models | 22 | 2.39e-01 | -1.45e-01 | 5.44e-01 |
| Neurodegenerative Diseases | 22 | 2.39e-01 | -1.45e-01 | 5.44e-01 |
| NFE2L2 regulating tumorigenic genes | 10 | 4.29e-01 | 1.44e-01 | 7.25e-01 |
| 2-LTR circle formation | 7 | 5.10e-01 | -1.44e-01 | 7.70e-01 |
| RUNX1 regulates transcription of genes involved in interleukin signaling | 5 | 5.78e-01 | 1.44e-01 | 8.15e-01 |
| Caspase activation via Dependence Receptors in the absence of ligand | 9 | 4.55e-01 | -1.44e-01 | 7.42e-01 |
| TNFR2 non-canonical NF-kB pathway | 95 | 1.57e-02 | -1.43e-01 | 8.82e-02 |
| Loss of Function of SMAD2/3 in Cancer | 7 | 5.13e-01 | -1.43e-01 | 7.71e-01 |
| MyD88 dependent cascade initiated on endosome | 96 | 1.56e-02 | -1.43e-01 | 8.79e-02 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 96 | 1.56e-02 | -1.43e-01 | 8.79e-02 |
| Regulation of KIT signaling | 16 | 3.23e-01 | 1.43e-01 | 6.26e-01 |
| Pyruvate metabolism and Citric Acid (TCA) cycle | 52 | 7.51e-02 | -1.43e-01 | 2.70e-01 |
| NOD1/2 Signaling Pathway | 33 | 1.56e-01 | -1.43e-01 | 4.26e-01 |
| DARPP-32 events | 24 | 2.27e-01 | -1.42e-01 | 5.28e-01 |
| Interleukin receptor SHC signaling | 23 | 2.38e-01 | -1.42e-01 | 5.44e-01 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 76 | 3.22e-02 | 1.42e-01 | 1.51e-01 |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | 8 | 4.86e-01 | 1.42e-01 | 7.63e-01 |
| Cellular responses to stress | 740 | 4.96e-11 | -1.42e-01 | 5.83e-09 |
| Relaxin receptors | 8 | 4.88e-01 | 1.42e-01 | 7.63e-01 |
| TP53 Regulates Transcription of Death Receptors and Ligands | 12 | 3.96e-01 | 1.41e-01 | 6.98e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE | 26 | 2.12e-01 | -1.41e-01 | 5.10e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 26 | 2.12e-01 | -1.41e-01 | 5.10e-01 |
| Senescence-Associated Secretory Phenotype (SASP) | 74 | 3.57e-02 | -1.41e-01 | 1.62e-01 |
| Arachidonic acid metabolism | 57 | 6.52e-02 | -1.41e-01 | 2.45e-01 |
| ATF4 activates genes in response to endoplasmic reticulum stress | 27 | 2.04e-01 | -1.41e-01 | 4.95e-01 |
| Inactivation of CDC42 and RAC1 | 8 | 4.90e-01 | 1.41e-01 | 7.63e-01 |
| Formation of RNA Pol II elongation complex | 57 | 6.58e-02 | -1.41e-01 | 2.46e-01 |
| RNA Polymerase II Transcription Elongation | 57 | 6.58e-02 | -1.41e-01 | 2.46e-01 |
| Neurotransmitter release cycle | 48 | 9.16e-02 | 1.41e-01 | 3.07e-01 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 20 | 2.77e-01 | 1.40e-01 | 5.78e-01 |
| Caspase activation via extrinsic apoptotic signalling pathway | 25 | 2.25e-01 | -1.40e-01 | 5.25e-01 |
| SUMOylation of DNA damage response and repair proteins | 74 | 3.74e-02 | -1.40e-01 | 1.66e-01 |
| Late Phase of HIV Life Cycle | 132 | 5.52e-03 | -1.40e-01 | 3.92e-02 |
| Transcriptional regulation by RUNX3 | 93 | 1.97e-02 | -1.40e-01 | 1.06e-01 |
| Transport of fatty acids | 8 | 4.94e-01 | 1.40e-01 | 7.64e-01 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 36 | 1.47e-01 | -1.40e-01 | 4.09e-01 |
| Regulation of RUNX2 expression and activity | 72 | 4.08e-02 | -1.39e-01 | 1.76e-01 |
| PERK regulates gene expression | 31 | 1.80e-01 | -1.39e-01 | 4.66e-01 |
| Conjugation of salicylate with glycine | 7 | 5.23e-01 | 1.39e-01 | 7.79e-01 |
| Chromosome Maintenance | 109 | 1.21e-02 | -1.39e-01 | 7.13e-02 |
| RUNX3 regulates p14-ARF | 10 | 4.47e-01 | 1.39e-01 | 7.38e-01 |
| Platelet sensitization by LDL | 17 | 3.22e-01 | -1.39e-01 | 6.25e-01 |
| Organelle biogenesis and maintenance | 274 | 7.69e-05 | -1.39e-01 | 1.71e-03 |
| SARS-CoV-1 Infection | 135 | 5.58e-03 | -1.38e-01 | 3.94e-02 |
| Caspase activation via Death Receptors in the presence of ligand | 16 | 3.39e-01 | -1.38e-01 | 6.44e-01 |
| Non-integrin membrane-ECM interactions | 55 | 7.65e-02 | 1.38e-01 | 2.73e-01 |
| Termination of O-glycan biosynthesis | 25 | 2.32e-01 | -1.38e-01 | 5.36e-01 |
| Erythropoietin activates RAS | 14 | 3.72e-01 | 1.38e-01 | 6.77e-01 |
| Response of Mtb to phagocytosis | 22 | 2.63e-01 | -1.38e-01 | 5.65e-01 |
| Signaling by FGFR4 in disease | 11 | 4.29e-01 | 1.38e-01 | 7.25e-01 |
| Signaling by NOTCH4 | 80 | 3.36e-02 | -1.37e-01 | 1.56e-01 |
| HDMs demethylate histones | 18 | 3.13e-01 | -1.37e-01 | 6.15e-01 |
| RHOBTB GTPase Cycle | 34 | 1.67e-01 | -1.37e-01 | 4.44e-01 |
| Cellular responses to stimuli | 754 | 1.59e-10 | -1.37e-01 | 1.77e-08 |
| Signaling by Retinoic Acid | 41 | 1.30e-01 | 1.37e-01 | 3.81e-01 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 27 | 2.19e-01 | -1.37e-01 | 5.18e-01 |
| G alpha (q) signalling events | 206 | 7.50e-04 | 1.36e-01 | 9.49e-03 |
| mRNA Editing | 10 | 4.56e-01 | -1.36e-01 | 7.42e-01 |
| IRAK1 recruits IKK complex | 12 | 4.14e-01 | -1.36e-01 | 7.11e-01 |
| IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | 12 | 4.14e-01 | -1.36e-01 | 7.11e-01 |
| DAP12 interactions | 37 | 1.52e-01 | -1.36e-01 | 4.19e-01 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | 112 | 1.29e-02 | -1.36e-01 | 7.50e-02 |
| Apoptosis | 172 | 2.11e-03 | -1.36e-01 | 1.95e-02 |
| Defects of platelet adhesion to exposed collagen | 8 | 5.07e-01 | 1.35e-01 | 7.69e-01 |
| Infection with Mycobacterium tuberculosis | 25 | 2.41e-01 | -1.35e-01 | 5.48e-01 |
| Processive synthesis on the lagging strand | 14 | 3.81e-01 | -1.35e-01 | 6.85e-01 |
| Interleukin-17 signaling | 66 | 5.79e-02 | -1.35e-01 | 2.25e-01 |
| Nucleotide Excision Repair | 107 | 1.64e-02 | -1.34e-01 | 9.06e-02 |
| Acyl chain remodelling of PS | 22 | 2.76e-01 | -1.34e-01 | 5.77e-01 |
| Collagen degradation | 61 | 7.02e-02 | 1.34e-01 | 2.56e-01 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 19 | 3.12e-01 | 1.34e-01 | 6.15e-01 |
| Synthesis of IP3 and IP4 in the cytosol | 25 | 2.47e-01 | -1.34e-01 | 5.50e-01 |
| MyD88-independent TLR4 cascade | 103 | 1.95e-02 | -1.33e-01 | 1.05e-01 |
| TRIF(TICAM1)-mediated TLR4 signaling | 103 | 1.95e-02 | -1.33e-01 | 1.05e-01 |
| DNA Repair | 298 | 7.71e-05 | -1.33e-01 | 1.71e-03 |
| Acetylcholine inhibits contraction of outer hair cells | 5 | 6.06e-01 | 1.33e-01 | 8.27e-01 |
| RNA Polymerase III Transcription Initiation | 36 | 1.67e-01 | -1.33e-01 | 4.44e-01 |
| Sodium/Calcium exchangers | 11 | 4.45e-01 | 1.33e-01 | 7.38e-01 |
| TNFR1-induced NF-kappa-B signaling pathway | 30 | 2.09e-01 | -1.33e-01 | 5.05e-01 |
| Attenuation phase | 24 | 2.61e-01 | 1.32e-01 | 5.65e-01 |
| Mitochondrial Uncoupling | 5 | 6.09e-01 | 1.32e-01 | 8.27e-01 |
| Activated NTRK3 signals through RAS | 8 | 5.18e-01 | 1.32e-01 | 7.76e-01 |
| PP2A-mediated dephosphorylation of key metabolic factors | 6 | 5.76e-01 | -1.32e-01 | 8.15e-01 |
| Toll Like Receptor 9 (TLR9) Cascade | 100 | 2.29e-02 | -1.32e-01 | 1.19e-01 |
| Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | 9 | 4.94e-01 | 1.32e-01 | 7.64e-01 |
| Regulation of pyruvate dehydrogenase (PDH) complex | 14 | 3.94e-01 | -1.32e-01 | 6.95e-01 |
| Signaling by Erythropoietin | 25 | 2.55e-01 | 1.31e-01 | 5.58e-01 |
| Protein repair | 6 | 5.78e-01 | -1.31e-01 | 8.15e-01 |
| Inwardly rectifying K+ channels | 35 | 1.80e-01 | 1.31e-01 | 4.66e-01 |
| NTRK2 activates RAC1 | 5 | 6.12e-01 | 1.31e-01 | 8.30e-01 |
| Interleukin-27 signaling | 11 | 4.53e-01 | -1.31e-01 | 7.42e-01 |
| Response of EIF2AK1 (HRI) to heme deficiency | 14 | 3.98e-01 | -1.30e-01 | 6.99e-01 |
| Fc epsilon receptor (FCERI) signaling | 127 | 1.14e-02 | -1.30e-01 | 6.94e-02 |
| Response to metal ions | 14 | 4.00e-01 | 1.30e-01 | 7.00e-01 |
| Signaling by Leptin | 11 | 4.56e-01 | 1.30e-01 | 7.42e-01 |
| Glutamate and glutamine metabolism | 12 | 4.36e-01 | -1.30e-01 | 7.32e-01 |
| ER to Golgi Anterograde Transport | 150 | 6.10e-03 | -1.30e-01 | 4.24e-02 |
| Bicarbonate transporters | 10 | 4.78e-01 | -1.30e-01 | 7.61e-01 |
| Cellular response to hypoxia | 73 | 5.56e-02 | -1.30e-01 | 2.19e-01 |
| Telomere C-strand (Lagging Strand) Synthesis | 33 | 2.01e-01 | -1.29e-01 | 4.92e-01 |
| Nectin/Necl trans heterodimerization | 7 | 5.56e-01 | 1.29e-01 | 8.02e-01 |
| Ca2+ pathway | 62 | 8.04e-02 | 1.28e-01 | 2.81e-01 |
| Diseases associated with O-glycosylation of proteins | 68 | 6.76e-02 | 1.28e-01 | 2.51e-01 |
| CTLA4 inhibitory signaling | 21 | 3.09e-01 | -1.28e-01 | 6.11e-01 |
| Disorders of transmembrane transporters | 170 | 3.97e-03 | -1.28e-01 | 3.11e-02 |
| MAPK3 (ERK1) activation | 10 | 4.83e-01 | -1.28e-01 | 7.61e-01 |
| Notch-HLH transcription pathway | 24 | 2.78e-01 | 1.28e-01 | 5.78e-01 |
| Regulation of gene expression by Hypoxia-inducible Factor | 10 | 4.84e-01 | 1.28e-01 | 7.62e-01 |
| Regulation of signaling by NODAL | 9 | 5.07e-01 | -1.28e-01 | 7.69e-01 |
| Acyl chain remodelling of PC | 27 | 2.51e-01 | -1.28e-01 | 5.55e-01 |
| Laminin interactions | 28 | 2.42e-01 | 1.28e-01 | 5.49e-01 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | 8 | 5.32e-01 | -1.28e-01 | 7.87e-01 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 20 | 3.24e-01 | -1.27e-01 | 6.26e-01 |
| Chemokine receptors bind chemokines | 53 | 1.09e-01 | 1.27e-01 | 3.43e-01 |
| FCGR3A-mediated phagocytosis | 56 | 1.01e-01 | -1.27e-01 | 3.24e-01 |
| Leishmania phagocytosis | 56 | 1.01e-01 | -1.27e-01 | 3.24e-01 |
| Parasite infection | 56 | 1.01e-01 | -1.27e-01 | 3.24e-01 |
| Processing of Intronless Pre-mRNAs | 19 | 3.40e-01 | -1.26e-01 | 6.45e-01 |
| Inhibition of DNA recombination at telomere | 43 | 1.52e-01 | -1.26e-01 | 4.19e-01 |
| RNA Polymerase III Abortive And Retractive Initiation | 41 | 1.63e-01 | -1.26e-01 | 4.38e-01 |
| RNA Polymerase III Transcription | 41 | 1.63e-01 | -1.26e-01 | 4.38e-01 |
| EGFR Transactivation by Gastrin | 9 | 5.13e-01 | 1.26e-01 | 7.71e-01 |
| MAPK6/MAPK4 signaling | 90 | 3.92e-02 | -1.26e-01 | 1.72e-01 |
| Degradation of cysteine and homocysteine | 14 | 4.15e-01 | 1.26e-01 | 7.13e-01 |
| Processing of Capped Intronless Pre-mRNA | 28 | 2.51e-01 | -1.25e-01 | 5.56e-01 |
| Regulation of TP53 Activity through Phosphorylation | 89 | 4.14e-02 | -1.25e-01 | 1.78e-01 |
| Signaling by CSF3 (G-CSF) | 30 | 2.36e-01 | -1.25e-01 | 5.42e-01 |
| Aspartate and asparagine metabolism | 11 | 4.74e-01 | 1.25e-01 | 7.61e-01 |
| GRB2 events in EGFR signaling | 12 | 4.56e-01 | 1.24e-01 | 7.42e-01 |
| Dissolution of Fibrin Clot | 13 | 4.38e-01 | 1.24e-01 | 7.32e-01 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 91 | 4.12e-02 | -1.24e-01 | 1.77e-01 |
| tRNA Aminoacylation | 40 | 1.75e-01 | -1.24e-01 | 4.60e-01 |
| COPI-mediated anterograde transport | 100 | 3.27e-02 | -1.24e-01 | 1.53e-01 |
| Formation of tubulin folding intermediates by CCT/TriC | 25 | 2.85e-01 | -1.23e-01 | 5.85e-01 |
| RSK activation | 5 | 6.33e-01 | -1.23e-01 | 8.42e-01 |
| mRNA Capping | 28 | 2.58e-01 | -1.23e-01 | 5.61e-01 |
| Chondroitin sulfate biosynthesis | 18 | 3.65e-01 | 1.23e-01 | 6.71e-01 |
| RHO GTPases Activate Rhotekin and Rhophilins | 8 | 5.47e-01 | -1.23e-01 | 7.97e-01 |
| Early SARS-CoV-2 Infection Events | 34 | 2.15e-01 | 1.23e-01 | 5.14e-01 |
| Transport and synthesis of PAPS | 6 | 6.03e-01 | 1.23e-01 | 8.27e-01 |
| Cellular response to chemical stress | 202 | 2.66e-03 | -1.23e-01 | 2.32e-02 |
| Sensory processing of sound by inner hair cells of the cochlea | 62 | 9.52e-02 | -1.23e-01 | 3.16e-01 |
| Disorders of Developmental Biology | 11 | 4.82e-01 | 1.22e-01 | 7.61e-01 |
| Disorders of Nervous System Development | 11 | 4.82e-01 | 1.22e-01 | 7.61e-01 |
| Loss of function of MECP2 in Rett syndrome | 11 | 4.82e-01 | 1.22e-01 | 7.61e-01 |
| Pervasive developmental disorders | 11 | 4.82e-01 | 1.22e-01 | 7.61e-01 |
| Formation of Incision Complex in GG-NER | 40 | 1.81e-01 | -1.22e-01 | 4.68e-01 |
| Translesion synthesis by REV1 | 16 | 3.98e-01 | -1.22e-01 | 6.99e-01 |
| Glycosaminoglycan metabolism | 120 | 2.11e-02 | 1.22e-01 | 1.13e-01 |
| TP53 Regulates Transcription of DNA Repair Genes | 61 | 1.00e-01 | -1.22e-01 | 3.24e-01 |
| Signaling by ERBB4 | 57 | 1.12e-01 | 1.22e-01 | 3.46e-01 |
| Scavenging by Class F Receptors | 6 | 6.06e-01 | -1.22e-01 | 8.27e-01 |
| Processing of DNA double-strand break ends | 75 | 7.04e-02 | -1.21e-01 | 2.56e-01 |
| Global Genome Nucleotide Excision Repair (GG-NER) | 81 | 6.02e-02 | -1.21e-01 | 2.31e-01 |
| Interleukin-1 family signaling | 146 | 1.18e-02 | -1.21e-01 | 7.01e-02 |
| SUMOylation of DNA methylation proteins | 16 | 4.03e-01 | 1.21e-01 | 7.02e-01 |
| Translesion synthesis by POLI | 17 | 3.90e-01 | -1.20e-01 | 6.90e-01 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 72 | 7.76e-02 | -1.20e-01 | 2.76e-01 |
| Phenylalanine and tyrosine metabolism | 11 | 4.90e-01 | -1.20e-01 | 7.63e-01 |
| Aspirin ADME | 38 | 2.00e-01 | 1.20e-01 | 4.92e-01 |
| Inactivation of CSF3 (G-CSF) signaling | 25 | 2.99e-01 | -1.20e-01 | 5.99e-01 |
| Digestion and absorption | 22 | 3.30e-01 | 1.20e-01 | 6.33e-01 |
| TICAM1-dependent activation of IRF3/IRF7 | 12 | 4.73e-01 | -1.20e-01 | 7.61e-01 |
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) | 15 | 4.23e-01 | -1.20e-01 | 7.18e-01 |
| Muscarinic acetylcholine receptors | 5 | 6.44e-01 | 1.19e-01 | 8.52e-01 |
| Hedgehog ‘off’ state | 110 | 3.08e-02 | -1.19e-01 | 1.46e-01 |
| TAK1-dependent IKK and NF-kappa-B activation | 41 | 1.87e-01 | -1.19e-01 | 4.78e-01 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | 20 | 3.58e-01 | 1.19e-01 | 6.66e-01 |
| Beta oxidation of butanoyl-CoA to acetyl-CoA | 5 | 6.46e-01 | 1.19e-01 | 8.53e-01 |
| Glycogen storage diseases | 15 | 4.26e-01 | -1.19e-01 | 7.21e-01 |
| Deubiquitination | 244 | 1.42e-03 | -1.19e-01 | 1.46e-02 |
| Regulation of actin dynamics for phagocytic cup formation | 57 | 1.22e-01 | -1.19e-01 | 3.66e-01 |
| Defective CHST14 causes EDS, musculocontractural type | 7 | 5.87e-01 | -1.19e-01 | 8.20e-01 |
| Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | 7 | 5.87e-01 | 1.19e-01 | 8.20e-01 |
| Binding of TCF/LEF:CTNNB1 to target gene promoters | 8 | 5.62e-01 | 1.18e-01 | 8.08e-01 |
| Condensation of Prophase Chromosomes | 36 | 2.19e-01 | -1.18e-01 | 5.18e-01 |
| AKT phosphorylates targets in the nucleus | 9 | 5.39e-01 | -1.18e-01 | 7.92e-01 |
| STAT3 nuclear events downstream of ALK signaling | 10 | 5.18e-01 | -1.18e-01 | 7.76e-01 |
| HS-GAG degradation | 21 | 3.49e-01 | 1.18e-01 | 6.55e-01 |
| Interleukin-18 signaling | 8 | 5.64e-01 | 1.18e-01 | 8.08e-01 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 106 | 3.64e-02 | -1.18e-01 | 1.64e-01 |
| Toll Like Receptor TLR6:TLR2 Cascade | 106 | 3.64e-02 | -1.18e-01 | 1.64e-01 |
| COPII-mediated vesicle transport | 65 | 1.02e-01 | -1.17e-01 | 3.27e-01 |
| Formation of the Editosome | 8 | 5.66e-01 | -1.17e-01 | 8.08e-01 |
| mRNA Editing: C to U Conversion | 8 | 5.66e-01 | -1.17e-01 | 8.08e-01 |
| Dual Incision in GG-NER | 39 | 2.06e-01 | -1.17e-01 | 4.99e-01 |
| Programmed Cell Death | 202 | 4.17e-03 | -1.17e-01 | 3.19e-02 |
| Insulin receptor recycling | 28 | 2.85e-01 | -1.17e-01 | 5.85e-01 |
| RHO GTPases activate CIT | 19 | 3.79e-01 | -1.17e-01 | 6.83e-01 |
| Regulation of cytoskeletal remodeling and cell spreading by IPP complex components | 7 | 5.93e-01 | -1.17e-01 | 8.20e-01 |
| Ub-specific processing proteases | 175 | 7.80e-03 | -1.17e-01 | 5.23e-02 |
| Nucleotide salvage | 21 | 3.55e-01 | -1.17e-01 | 6.63e-01 |
| Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane | 10 | 5.23e-01 | -1.17e-01 | 7.79e-01 |
| Formation of the cornified envelope | 123 | 2.58e-02 | 1.16e-01 | 1.28e-01 |
| Mitochondrial Fatty Acid Beta-Oxidation | 36 | 2.27e-01 | -1.16e-01 | 5.28e-01 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 11 | 5.05e-01 | -1.16e-01 | 7.68e-01 |
| Biosynthesis of specialized proresolving mediators (SPMs) | 19 | 3.82e-01 | 1.16e-01 | 6.85e-01 |
| DNA Double Strand Break Response | 56 | 1.34e-01 | -1.16e-01 | 3.86e-01 |
| Cilium Assembly | 190 | 6.00e-03 | -1.16e-01 | 4.18e-02 |
| Intrinsic Pathway for Apoptosis | 53 | 1.46e-01 | -1.16e-01 | 4.07e-01 |
| Interleukin-37 signaling | 20 | 3.72e-01 | 1.15e-01 | 6.77e-01 |
| Pentose phosphate pathway | 12 | 4.89e-01 | -1.15e-01 | 7.63e-01 |
| Protein-protein interactions at synapses | 78 | 7.90e-02 | 1.15e-01 | 2.78e-01 |
| Tryptophan catabolism | 14 | 4.57e-01 | 1.15e-01 | 7.43e-01 |
| Nef mediated downregulation of MHC class I complex cell surface expression | 8 | 5.74e-01 | 1.15e-01 | 8.15e-01 |
| Regulation of TLR by endogenous ligand | 21 | 3.63e-01 | 1.15e-01 | 6.68e-01 |
| Cytosolic iron-sulfur cluster assembly | 12 | 4.93e-01 | -1.14e-01 | 7.63e-01 |
| Synthesis of bile acids and bile salts via 27-hydroxycholesterol | 15 | 4.43e-01 | 1.14e-01 | 7.36e-01 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 49 | 1.66e-01 | -1.14e-01 | 4.43e-01 |
| Calnexin/calreticulin cycle | 26 | 3.14e-01 | -1.14e-01 | 6.15e-01 |
| Interleukin-7 signaling | 21 | 3.65e-01 | 1.14e-01 | 6.71e-01 |
| COPI-dependent Golgi-to-ER retrograde traffic | 98 | 5.10e-02 | -1.14e-01 | 2.07e-01 |
| FGFR1b ligand binding and activation | 8 | 5.77e-01 | 1.14e-01 | 8.15e-01 |
| RHOT2 GTPase cycle | 7 | 6.02e-01 | -1.14e-01 | 8.26e-01 |
| Leading Strand Synthesis | 13 | 4.78e-01 | -1.14e-01 | 7.61e-01 |
| Polymerase switching | 13 | 4.78e-01 | -1.14e-01 | 7.61e-01 |
| Disinhibition of SNARE formation | 5 | 6.60e-01 | 1.14e-01 | 8.59e-01 |
| Diseases of hemostasis | 17 | 4.18e-01 | 1.13e-01 | 7.15e-01 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 35 | 2.46e-01 | -1.13e-01 | 5.50e-01 |
| FLT3 signaling by CBL mutants | 7 | 6.04e-01 | -1.13e-01 | 8.27e-01 |
| Signal regulatory protein family interactions | 15 | 4.49e-01 | -1.13e-01 | 7.38e-01 |
| KEAP1-NFE2L2 pathway | 123 | 3.05e-02 | -1.13e-01 | 1.45e-01 |
| Fcgamma receptor (FCGR) dependent phagocytosis | 82 | 7.71e-02 | -1.13e-01 | 2.75e-01 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 13 | 4.81e-01 | -1.13e-01 | 7.61e-01 |
| Gluconeogenesis | 34 | 2.55e-01 | -1.13e-01 | 5.58e-01 |
| eNOS activation | 10 | 5.38e-01 | 1.13e-01 | 7.92e-01 |
| Estrogen biosynthesis | 6 | 6.33e-01 | -1.12e-01 | 8.42e-01 |
| Negative regulation of FGFR3 signaling | 28 | 3.04e-01 | 1.12e-01 | 6.04e-01 |
| IFNG signaling activates MAPKs | 8 | 5.83e-01 | 1.12e-01 | 8.18e-01 |
| Spry regulation of FGF signaling | 16 | 4.38e-01 | -1.12e-01 | 7.32e-01 |
| mTORC1-mediated signalling | 23 | 3.53e-01 | -1.12e-01 | 6.61e-01 |
| MET activates RAP1 and RAC1 | 11 | 5.21e-01 | -1.12e-01 | 7.78e-01 |
| Nuclear events stimulated by ALK signaling in cancer | 34 | 2.60e-01 | 1.12e-01 | 5.63e-01 |
| Recognition of DNA damage by PCNA-containing replication complex | 29 | 2.99e-01 | -1.12e-01 | 5.99e-01 |
| RHO GTPases activate IQGAPs | 30 | 2.90e-01 | -1.12e-01 | 5.91e-01 |
| Sodium-coupled sulphate, di- and tri-carboxylate transporters | 5 | 6.67e-01 | -1.11e-01 | 8.63e-01 |
| Lipophagy | 9 | 5.64e-01 | -1.11e-01 | 8.08e-01 |
| Viral Infection Pathways | 749 | 2.27e-07 | -1.11e-01 | 8.89e-06 |
| Nonhomologous End-Joining (NHEJ) | 46 | 1.92e-01 | -1.11e-01 | 4.84e-01 |
| Interaction between L1 and Ankyrins | 30 | 2.93e-01 | -1.11e-01 | 5.93e-01 |
| Lagging Strand Synthesis | 19 | 4.02e-01 | -1.11e-01 | 7.02e-01 |
| Sensory processing of sound | 69 | 1.11e-01 | -1.11e-01 | 3.46e-01 |
| Acyl chain remodelling of PE | 29 | 3.01e-01 | -1.11e-01 | 6.01e-01 |
| Signaling by FGFR1 | 51 | 1.71e-01 | 1.11e-01 | 4.52e-01 |
| POLB-Dependent Long Patch Base Excision Repair | 8 | 5.88e-01 | -1.11e-01 | 8.20e-01 |
| Asparagine N-linked glycosylation | 297 | 1.05e-03 | -1.11e-01 | 1.17e-02 |
| Regulation of signaling by CBL | 22 | 3.70e-01 | -1.10e-01 | 6.77e-01 |
| Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 10 | 5.47e-01 | -1.10e-01 | 7.97e-01 |
| Aflatoxin activation and detoxification | 19 | 4.06e-01 | -1.10e-01 | 7.05e-01 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 27 | 3.23e-01 | 1.10e-01 | 6.26e-01 |
| Peptide hormone metabolism | 81 | 8.77e-02 | 1.10e-01 | 2.99e-01 |
| Cyclin D associated events in G1 | 46 | 1.98e-01 | -1.10e-01 | 4.90e-01 |
| G1 Phase | 46 | 1.98e-01 | -1.10e-01 | 4.90e-01 |
| Gamma-carboxylation of protein precursors | 8 | 5.91e-01 | 1.10e-01 | 8.20e-01 |
| RUNX2 regulates genes involved in cell migration | 8 | 5.91e-01 | 1.10e-01 | 8.20e-01 |
| Signaling by FGFR2 IIIa TM | 19 | 4.09e-01 | -1.09e-01 | 7.07e-01 |
| ER Quality Control Compartment (ERQC) | 21 | 3.86e-01 | -1.09e-01 | 6.89e-01 |
| Transmission across Chemical Synapses | 255 | 2.72e-03 | 1.09e-01 | 2.36e-02 |
| HCMV Infection | 123 | 3.68e-02 | -1.09e-01 | 1.65e-01 |
| Formation of HIV elongation complex in the absence of HIV Tat | 44 | 2.11e-01 | -1.09e-01 | 5.08e-01 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | 51 | 1.78e-01 | -1.09e-01 | 4.64e-01 |
| Glucocorticoid biosynthesis | 9 | 5.71e-01 | 1.09e-01 | 8.14e-01 |
| Glyoxylate metabolism and glycine degradation | 30 | 3.02e-01 | -1.09e-01 | 6.02e-01 |
| Activation of the pre-replicative complex | 31 | 2.94e-01 | -1.09e-01 | 5.95e-01 |
| Ubiquinol biosynthesis | 8 | 5.94e-01 | -1.09e-01 | 8.20e-01 |
| Translesion Synthesis by POLH | 18 | 4.25e-01 | -1.09e-01 | 7.19e-01 |
| tRNA modification in the nucleus and cytosol | 41 | 2.29e-01 | -1.09e-01 | 5.30e-01 |
| SHC1 events in EGFR signaling | 13 | 4.98e-01 | 1.08e-01 | 7.65e-01 |
| Apoptosis induced DNA fragmentation | 13 | 4.99e-01 | -1.08e-01 | 7.65e-01 |
| Ephrin signaling | 17 | 4.39e-01 | -1.08e-01 | 7.32e-01 |
| Toll Like Receptor 2 (TLR2) Cascade | 109 | 5.07e-02 | -1.08e-01 | 2.07e-01 |
| Toll Like Receptor TLR1:TLR2 Cascade | 109 | 5.07e-02 | -1.08e-01 | 2.07e-01 |
| Apoptotic cleavage of cell adhesion proteins | 11 | 5.35e-01 | 1.08e-01 | 7.90e-01 |
| Signaling by WNT in cancer | 32 | 2.91e-01 | 1.08e-01 | 5.91e-01 |
| Transport of nucleotide sugars | 8 | 5.97e-01 | 1.08e-01 | 8.22e-01 |
| MAPK1 (ERK2) activation | 9 | 5.75e-01 | -1.08e-01 | 8.15e-01 |
| APC truncation mutants have impaired AXIN binding | 13 | 5.01e-01 | -1.08e-01 | 7.65e-01 |
| AXIN missense mutants destabilize the destruction complex | 13 | 5.01e-01 | -1.08e-01 | 7.65e-01 |
| Signaling by AMER1 mutants | 13 | 5.01e-01 | -1.08e-01 | 7.65e-01 |
| Signaling by APC mutants | 13 | 5.01e-01 | -1.08e-01 | 7.65e-01 |
| Signaling by AXIN mutants | 13 | 5.01e-01 | -1.08e-01 | 7.65e-01 |
| Truncations of AMER1 destabilize the destruction complex | 13 | 5.01e-01 | -1.08e-01 | 7.65e-01 |
| Negative regulation of FGFR2 signaling | 33 | 2.84e-01 | 1.08e-01 | 5.84e-01 |
| RHO GTPases activate PKNs | 56 | 1.65e-01 | -1.07e-01 | 4.42e-01 |
| Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) | 9 | 5.78e-01 | 1.07e-01 | 8.15e-01 |
| Scavenging by Class B Receptors | 6 | 6.50e-01 | 1.07e-01 | 8.53e-01 |
| Interleukin-6 signaling | 11 | 5.40e-01 | -1.07e-01 | 7.93e-01 |
| RHO GTPases activate PAKs | 19 | 4.21e-01 | -1.07e-01 | 7.16e-01 |
| Telomere Extension By Telomerase | 22 | 3.87e-01 | -1.07e-01 | 6.89e-01 |
| HCMV Early Events | 99 | 6.70e-02 | -1.07e-01 | 2.49e-01 |
| Innate Immune System | 987 | 1.52e-08 | -1.06e-01 | 8.42e-07 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 17 | 4.48e-01 | -1.06e-01 | 7.38e-01 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 17 | 4.48e-01 | -1.06e-01 | 7.38e-01 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 44 | 2.23e-01 | -1.06e-01 | 5.24e-01 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | 23 | 3.78e-01 | -1.06e-01 | 6.83e-01 |
| CTNNB1 S33 mutants aren’t phosphorylated | 14 | 4.92e-01 | -1.06e-01 | 7.63e-01 |
| CTNNB1 S37 mutants aren’t phosphorylated | 14 | 4.92e-01 | -1.06e-01 | 7.63e-01 |
| CTNNB1 S45 mutants aren’t phosphorylated | 14 | 4.92e-01 | -1.06e-01 | 7.63e-01 |
| CTNNB1 T41 mutants aren’t phosphorylated | 14 | 4.92e-01 | -1.06e-01 | 7.63e-01 |
| Signaling by CTNNB1 phospho-site mutants | 14 | 4.92e-01 | -1.06e-01 | 7.63e-01 |
| Signaling by GSK3beta mutants | 14 | 4.92e-01 | -1.06e-01 | 7.63e-01 |
| Interleukin-2 signaling | 11 | 5.44e-01 | -1.06e-01 | 7.95e-01 |
| O-linked glycosylation | 110 | 5.57e-02 | 1.06e-01 | 2.19e-01 |
| N-Glycan antennae elongation | 15 | 4.79e-01 | 1.06e-01 | 7.61e-01 |
| Dual incision in TC-NER | 63 | 1.48e-01 | -1.05e-01 | 4.10e-01 |
| DCC mediated attractive signaling | 14 | 4.95e-01 | -1.05e-01 | 7.64e-01 |
| Pexophagy | 10 | 5.64e-01 | -1.05e-01 | 8.08e-01 |
| Glycogen breakdown (glycogenolysis) | 11 | 5.46e-01 | 1.05e-01 | 7.97e-01 |
| PTK6 promotes HIF1A stabilization | 7 | 6.30e-01 | 1.05e-01 | 8.40e-01 |
| RHOJ GTPase cycle | 50 | 1.98e-01 | 1.05e-01 | 4.90e-01 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 38 | 2.62e-01 | -1.05e-01 | 5.65e-01 |
| Organic cation/anion/zwitterion transport | 15 | 4.83e-01 | -1.05e-01 | 7.61e-01 |
| Transport to the Golgi and subsequent modification | 181 | 1.53e-02 | -1.04e-01 | 8.73e-02 |
| RHOBTB1 GTPase cycle | 22 | 3.97e-01 | -1.04e-01 | 6.98e-01 |
| Interconversion of nucleotide di- and triphosphates | 29 | 3.31e-01 | -1.04e-01 | 6.34e-01 |
| ARMS-mediated activation | 7 | 6.33e-01 | -1.04e-01 | 8.42e-01 |
| Mitochondrial tRNA aminoacylation | 20 | 4.20e-01 | -1.04e-01 | 7.15e-01 |
| Plasma lipoprotein assembly | 19 | 4.33e-01 | 1.04e-01 | 7.28e-01 |
| RHOBTB2 GTPase cycle | 22 | 4.00e-01 | -1.04e-01 | 7.00e-01 |
| RHOF GTPase cycle | 40 | 2.58e-01 | 1.03e-01 | 5.60e-01 |
| Meiotic recombination | 50 | 2.06e-01 | -1.03e-01 | 4.99e-01 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | 29 | 3.36e-01 | -1.03e-01 | 6.41e-01 |
| PCNA-Dependent Long Patch Base Excision Repair | 21 | 4.14e-01 | -1.03e-01 | 7.11e-01 |
| SUMOylation of immune response proteins | 11 | 5.55e-01 | -1.03e-01 | 8.02e-01 |
| Recycling pathway of L1 | 42 | 2.49e-01 | -1.03e-01 | 5.53e-01 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 28 | 3.47e-01 | -1.03e-01 | 6.53e-01 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 55 | 1.88e-01 | -1.03e-01 | 4.78e-01 |
| PKR-mediated signaling | 70 | 1.38e-01 | -1.03e-01 | 3.95e-01 |
| PIWI-interacting RNA (piRNA) biogenesis | 29 | 3.41e-01 | -1.02e-01 | 6.46e-01 |
| Long-term potentiation | 22 | 4.06e-01 | 1.02e-01 | 7.05e-01 |
| Phosphorylation of CD3 and TCR zeta chains | 16 | 4.80e-01 | 1.02e-01 | 7.61e-01 |
| Selective autophagy | 76 | 1.25e-01 | -1.02e-01 | 3.73e-01 |
| Nef Mediated CD4 Down-regulation | 9 | 5.98e-01 | 1.02e-01 | 8.22e-01 |
| Activation of RAC1 downstream of NMDARs | 7 | 6.42e-01 | -1.02e-01 | 8.51e-01 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 76 | 1.27e-01 | -1.01e-01 | 3.77e-01 |
| Prolactin receptor signaling | 13 | 5.28e-01 | 1.01e-01 | 7.82e-01 |
| Deactivation of the beta-catenin transactivating complex | 39 | 2.76e-01 | 1.01e-01 | 5.77e-01 |
| Synthesis, secretion, and deacylation of Ghrelin | 18 | 4.59e-01 | 1.01e-01 | 7.45e-01 |
| SUMOylation of chromatin organization proteins | 57 | 1.89e-01 | -1.01e-01 | 4.79e-01 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | 198 | 1.51e-02 | -1.00e-01 | 8.63e-02 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 76 | 1.31e-01 | -1.00e-01 | 3.82e-01 |
| Signal attenuation | 10 | 5.85e-01 | 9.98e-02 | 8.19e-01 |
| Intraflagellar transport | 51 | 2.18e-01 | -9.97e-02 | 5.18e-01 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 42 | 2.64e-01 | -9.95e-02 | 5.65e-01 |
| HIV Transcription Elongation | 42 | 2.64e-01 | -9.95e-02 | 5.65e-01 |
| Tat-mediated elongation of the HIV-1 transcript | 42 | 2.64e-01 | -9.95e-02 | 5.65e-01 |
| IL-6-type cytokine receptor ligand interactions | 17 | 4.77e-01 | 9.95e-02 | 7.61e-01 |
| TBC/RABGAPs | 41 | 2.71e-01 | -9.94e-02 | 5.74e-01 |
| Neutrophil degranulation | 453 | 2.86e-04 | -9.94e-02 | 5.06e-03 |
| Formation of Fibrin Clot (Clotting Cascade) | 37 | 2.96e-01 | 9.93e-02 | 5.96e-01 |
| RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | 9 | 6.06e-01 | -9.93e-02 | 8.27e-01 |
| Post-translational modification: synthesis of GPI-anchored proteins | 90 | 1.04e-01 | 9.92e-02 | 3.33e-01 |
| Biotin transport and metabolism | 10 | 5.88e-01 | 9.88e-02 | 8.20e-01 |
| Interleukin-2 family signaling | 39 | 2.86e-01 | -9.87e-02 | 5.86e-01 |
| Signaling by ERBB2 ECD mutants | 16 | 4.95e-01 | 9.85e-02 | 7.64e-01 |
| Diseases associated with surfactant metabolism | 9 | 6.09e-01 | 9.85e-02 | 8.27e-01 |
| Activation of the phototransduction cascade | 11 | 5.72e-01 | 9.83e-02 | 8.14e-01 |
| Sodium-coupled phosphate cotransporters | 5 | 7.03e-01 | -9.83e-02 | 8.88e-01 |
| TNFR1-induced proapoptotic signaling | 24 | 4.05e-01 | -9.83e-02 | 7.04e-01 |
| RHOQ GTPase cycle | 57 | 2.00e-01 | 9.82e-02 | 4.92e-01 |
| Mucopolysaccharidoses | 10 | 5.91e-01 | 9.81e-02 | 8.20e-01 |
| TICAM1,TRAF6-dependent induction of TAK1 complex | 10 | 5.92e-01 | -9.78e-02 | 8.20e-01 |
| Serotonin Neurotransmitter Release Cycle | 17 | 4.85e-01 | 9.77e-02 | 7.62e-01 |
| Metabolism of porphyrins | 26 | 3.88e-01 | -9.77e-02 | 6.89e-01 |
| ECM proteoglycans | 73 | 1.50e-01 | 9.75e-02 | 4.14e-01 |
| Binding and Uptake of Ligands by Scavenger Receptors | 41 | 2.81e-01 | -9.73e-02 | 5.82e-01 |
| Infectious disease | 931 | 4.94e-07 | -9.72e-02 | 1.86e-05 |
| Atorvastatin ADME | 9 | 6.14e-01 | 9.70e-02 | 8.30e-01 |
| Synthesis of PIPs at the Golgi membrane | 17 | 4.90e-01 | 9.68e-02 | 7.63e-01 |
| Meiosis | 80 | 1.35e-01 | -9.67e-02 | 3.87e-01 |
| Formation of WDR5-containing histone-modifying complexes | 38 | 3.02e-01 | -9.67e-02 | 6.02e-01 |
| Extracellular matrix organization | 291 | 4.63e-03 | 9.65e-02 | 3.43e-02 |
| Collagen formation | 88 | 1.19e-01 | 9.61e-02 | 3.60e-01 |
| TRIF-mediated programmed cell death | 9 | 6.18e-01 | 9.60e-02 | 8.30e-01 |
| Golgi-to-ER retrograde transport | 132 | 5.69e-02 | -9.60e-02 | 2.22e-01 |
| Androgen biosynthesis | 11 | 5.82e-01 | -9.57e-02 | 8.18e-01 |
| SARS-CoV-2 Infection | 273 | 6.48e-03 | -9.57e-02 | 4.45e-02 |
| Cellular hexose transport | 22 | 4.38e-01 | -9.56e-02 | 7.32e-01 |
| VEGFR2 mediated cell proliferation | 19 | 4.71e-01 | 9.56e-02 | 7.59e-01 |
| RUNX3 regulates WNT signaling | 8 | 6.40e-01 | 9.55e-02 | 8.50e-01 |
| Neurotransmitter receptors and postsynaptic signal transmission | 192 | 2.26e-02 | 9.54e-02 | 1.18e-01 |
| Recycling of bile acids and salts | 18 | 4.85e-01 | -9.51e-02 | 7.62e-01 |
| DNA Damage Bypass | 46 | 2.65e-01 | -9.49e-02 | 5.66e-01 |
| Asymmetric localization of PCP proteins | 63 | 1.93e-01 | -9.49e-02 | 4.84e-01 |
| Negative regulation of FGFR1 signaling | 32 | 3.53e-01 | 9.48e-02 | 6.61e-01 |
| RNA Polymerase II Pre-transcription Events | 77 | 1.52e-01 | -9.45e-02 | 4.19e-01 |
| Beta-catenin phosphorylation cascade | 16 | 5.13e-01 | -9.44e-02 | 7.71e-01 |
| Activation of G protein gated Potassium channels | 29 | 3.79e-01 | 9.44e-02 | 6.83e-01 |
| G protein gated Potassium channels | 29 | 3.79e-01 | 9.44e-02 | 6.83e-01 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 29 | 3.79e-01 | 9.44e-02 | 6.83e-01 |
| HSF1 activation | 26 | 4.08e-01 | 9.37e-02 | 7.06e-01 |
| B-WICH complex positively regulates rRNA expression | 54 | 2.34e-01 | -9.36e-02 | 5.39e-01 |
| Defective RIPK1-mediated regulated necrosis | 7 | 6.68e-01 | 9.36e-02 | 8.63e-01 |
| Pre-NOTCH Expression and Processing | 83 | 1.43e-01 | 9.31e-02 | 4.00e-01 |
| NFE2L2 regulating ER-stress associated genes | 5 | 7.19e-01 | 9.30e-02 | 8.96e-01 |
| Negative regulation of MET activity | 20 | 4.72e-01 | -9.30e-02 | 7.60e-01 |
| Extension of Telomeres | 49 | 2.60e-01 | -9.29e-02 | 5.64e-01 |
| VLDL assembly | 5 | 7.19e-01 | 9.28e-02 | 8.96e-01 |
| Metabolism of amino acids and derivatives | 351 | 2.82e-03 | -9.28e-02 | 2.41e-02 |
| Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA | 6 | 6.94e-01 | -9.27e-02 | 8.83e-01 |
| Retrograde neurotrophin signalling | 14 | 5.49e-01 | 9.26e-02 | 7.98e-01 |
| Protein folding | 95 | 1.19e-01 | -9.25e-02 | 3.60e-01 |
| IRAK4 deficiency (TLR2/4) | 17 | 5.09e-01 | 9.25e-02 | 7.70e-01 |
| Cell junction organization | 113 | 8.95e-02 | 9.25e-02 | 3.02e-01 |
| Telomere Maintenance | 86 | 1.38e-01 | -9.24e-02 | 3.95e-01 |
| Collagen chain trimerization | 42 | 3.03e-01 | 9.19e-02 | 6.02e-01 |
| Activated NTRK2 signals through FYN | 7 | 6.74e-01 | 9.19e-02 | 8.65e-01 |
| Neurotoxicity of clostridium toxins | 10 | 6.16e-01 | 9.17e-02 | 8.30e-01 |
| Nuclear Events (kinase and transcription factor activation) | 59 | 2.24e-01 | -9.15e-02 | 5.25e-01 |
| Loss of Function of TGFBR1 in Cancer | 7 | 6.75e-01 | -9.14e-02 | 8.65e-01 |
| Formation of paraxial mesoderm | 67 | 1.96e-01 | -9.13e-02 | 4.90e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 14 | 5.54e-01 | -9.12e-02 | 8.02e-01 |
| Interleukin-10 signaling | 41 | 3.14e-01 | -9.08e-02 | 6.16e-01 |
| TP53 Regulates Transcription of Cell Cycle Genes | 48 | 2.76e-01 | -9.08e-02 | 5.77e-01 |
| Toxicity of botulinum toxin type D (botD) | 5 | 7.25e-01 | 9.07e-02 | 9.01e-01 |
| Toxicity of botulinum toxin type F (botF) | 5 | 7.25e-01 | 9.07e-02 | 9.01e-01 |
| Formation of TC-NER Pre-Incision Complex | 51 | 2.63e-01 | -9.06e-02 | 5.65e-01 |
| Retrograde transport at the Trans-Golgi-Network | 47 | 2.83e-01 | -9.05e-02 | 5.84e-01 |
| Signaling by Insulin receptor | 79 | 1.64e-01 | 9.05e-02 | 4.41e-01 |
| PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 14 | 5.59e-01 | -9.01e-02 | 8.06e-01 |
| Regulated Necrosis | 56 | 2.45e-01 | -8.98e-02 | 5.50e-01 |
| Pregnenolone biosynthesis | 12 | 5.90e-01 | 8.98e-02 | 8.20e-01 |
| TRP channels | 27 | 4.19e-01 | 8.98e-02 | 7.15e-01 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 13 | 5.76e-01 | 8.95e-02 | 8.15e-01 |
| Downregulation of ERBB2:ERBB3 signaling | 13 | 5.77e-01 | -8.93e-02 | 8.15e-01 |
| VEGFR2 mediated vascular permeability | 26 | 4.32e-01 | 8.90e-02 | 7.27e-01 |
| Branched-chain amino acid catabolism | 20 | 4.92e-01 | 8.89e-02 | 7.63e-01 |
| p75NTR signals via NF-kB | 15 | 5.51e-01 | -8.89e-02 | 8.01e-01 |
| Metabolism of nucleotides | 93 | 1.40e-01 | -8.86e-02 | 3.96e-01 |
| Signaling by Interleukins | 429 | 1.68e-03 | -8.84e-02 | 1.65e-02 |
| Regulation of IFNA/IFNB signaling | 18 | 5.19e-01 | 8.79e-02 | 7.76e-01 |
| VxPx cargo-targeting to cilium | 20 | 4.97e-01 | 8.78e-02 | 7.65e-01 |
| Mismatch Repair | 15 | 5.57e-01 | -8.76e-02 | 8.03e-01 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | 25 | 4.50e-01 | -8.73e-02 | 7.39e-01 |
| Amino acids regulate mTORC1 | 51 | 2.81e-01 | -8.72e-02 | 5.82e-01 |
| Biosynthesis of E-series 18(S)-resolvins | 5 | 7.36e-01 | 8.71e-02 | 9.04e-01 |
| NADE modulates death signalling | 5 | 7.36e-01 | -8.71e-02 | 9.04e-01 |
| Regulation of NF-kappa B signaling | 17 | 5.35e-01 | -8.70e-02 | 7.90e-01 |
| Highly calcium permeable postsynaptic nicotinic acetylcholine receptors | 11 | 6.18e-01 | 8.69e-02 | 8.30e-01 |
| NRAGE signals death through JNK | 53 | 2.75e-01 | 8.67e-02 | 5.76e-01 |
| Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) | 8 | 6.71e-01 | 8.67e-02 | 8.64e-01 |
| The role of Nef in HIV-1 replication and disease pathogenesis | 26 | 4.44e-01 | 8.66e-02 | 7.37e-01 |
| Packaging Of Telomere Ends | 29 | 4.20e-01 | -8.66e-02 | 7.15e-01 |
| Chaperonin-mediated protein folding | 89 | 1.58e-01 | -8.66e-02 | 4.29e-01 |
| Role of second messengers in netrin-1 signaling | 9 | 6.53e-01 | 8.65e-02 | 8.54e-01 |
| CS/DS degradation | 12 | 6.04e-01 | -8.64e-02 | 8.27e-01 |
| RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | 8 | 6.73e-01 | 8.63e-02 | 8.65e-01 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 53 | 2.77e-01 | -8.63e-02 | 5.78e-01 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 70 | 2.13e-01 | -8.61e-02 | 5.10e-01 |
| Activation of gene expression by SREBF (SREBP) | 41 | 3.41e-01 | -8.59e-02 | 6.46e-01 |
| Downregulation of TGF-beta receptor signaling | 26 | 4.49e-01 | -8.59e-02 | 7.38e-01 |
| Chondroitin sulfate/dermatan sulfate metabolism | 45 | 3.20e-01 | 8.57e-02 | 6.22e-01 |
| Diseases of programmed cell death | 66 | 2.29e-01 | -8.56e-02 | 5.30e-01 |
| Glucuronidation | 20 | 5.08e-01 | 8.55e-02 | 7.70e-01 |
| G alpha (s) signalling events | 155 | 6.70e-02 | 8.52e-02 | 2.49e-01 |
| MyD88 deficiency (TLR2/4) | 16 | 5.55e-01 | 8.52e-02 | 8.02e-01 |
| Apoptotic cleavage of cellular proteins | 35 | 3.84e-01 | -8.50e-02 | 6.87e-01 |
| NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis | 9 | 6.60e-01 | -8.48e-02 | 8.59e-01 |
| SUMOylation of transcription factors | 20 | 5.13e-01 | 8.44e-02 | 7.71e-01 |
| Negative regulation of FGFR4 signaling | 30 | 4.24e-01 | 8.44e-02 | 7.19e-01 |
| Negative regulation of the PI3K/AKT network | 110 | 1.26e-01 | 8.43e-02 | 3.77e-01 |
| Cleavage of the damaged purine | 33 | 4.03e-01 | -8.41e-02 | 7.02e-01 |
| Depurination | 33 | 4.03e-01 | -8.41e-02 | 7.02e-01 |
| Recognition and association of DNA glycosylase with site containing an affected purine | 33 | 4.03e-01 | -8.41e-02 | 7.02e-01 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 29 | 4.35e-01 | -8.38e-02 | 7.30e-01 |
| N-glycan trimming and elongation in the cis-Golgi | 5 | 7.46e-01 | -8.36e-02 | 9.10e-01 |
| Cardiac conduction | 125 | 1.07e-01 | 8.35e-02 | 3.39e-01 |
| Assembly and cell surface presentation of NMDA receptors | 40 | 3.61e-01 | 8.34e-02 | 6.67e-01 |
| Signaling by TGF-beta Receptor Complex | 92 | 1.68e-01 | -8.32e-02 | 4.44e-01 |
| Molecules associated with elastic fibres | 37 | 3.81e-01 | 8.32e-02 | 6.85e-01 |
| trans-Golgi Network Vesicle Budding | 67 | 2.40e-01 | -8.31e-02 | 5.45e-01 |
| SARS-CoV Infections | 384 | 5.26e-03 | -8.30e-02 | 3.77e-02 |
| Membrane binding and targetting of GAG proteins | 14 | 5.92e-01 | -8.28e-02 | 8.20e-01 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 14 | 5.92e-01 | -8.28e-02 | 8.20e-01 |
| Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA | 5 | 7.49e-01 | 8.27e-02 | 9.10e-01 |
| Hedgehog ‘on’ state | 85 | 1.89e-01 | -8.25e-02 | 4.78e-01 |
| Fatty acid metabolism | 171 | 6.28e-02 | -8.25e-02 | 2.39e-01 |
| MECP2 regulates transcription of neuronal ligands | 7 | 7.06e-01 | 8.23e-02 | 8.91e-01 |
| Carnitine metabolism | 13 | 6.07e-01 | 8.23e-02 | 8.27e-01 |
| Defective HLCS causes multiple carboxylase deficiency | 7 | 7.07e-01 | 8.22e-02 | 8.91e-01 |
| RHOD GTPase cycle | 49 | 3.20e-01 | 8.20e-02 | 6.23e-01 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 37 | 3.88e-01 | 8.20e-02 | 6.89e-01 |
| Signaling by FGFR3 | 39 | 3.77e-01 | 8.18e-02 | 6.83e-01 |
| Signaling by FGFR4 | 40 | 3.72e-01 | 8.16e-02 | 6.77e-01 |
| Beta defensins | 24 | 4.90e-01 | 8.15e-02 | 7.63e-01 |
| Reproduction | 117 | 1.29e-01 | -8.13e-02 | 3.79e-01 |
| HATs acetylate histones | 97 | 1.66e-01 | -8.13e-02 | 4.43e-01 |
| Signaling by NTRK2 (TRKB) | 25 | 4.82e-01 | 8.13e-02 | 7.61e-01 |
| FOXO-mediated transcription of cell death genes | 15 | 5.86e-01 | 8.12e-02 | 8.20e-01 |
| Toll Like Receptor 4 (TLR4) Cascade | 138 | 1.00e-01 | -8.11e-02 | 3.24e-01 |
| Signaling by PDGF | 57 | 2.90e-01 | 8.11e-02 | 5.91e-01 |
| Axon guidance | 527 | 1.47e-03 | -8.10e-02 | 1.49e-02 |
| Cleavage of the damaged pyrimidine | 38 | 3.89e-01 | -8.08e-02 | 6.89e-01 |
| Depyrimidination | 38 | 3.89e-01 | -8.08e-02 | 6.89e-01 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 38 | 3.89e-01 | -8.08e-02 | 6.89e-01 |
| Mitochondrial calcium ion transport | 21 | 5.22e-01 | -8.07e-02 | 7.78e-01 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 29 | 4.52e-01 | 8.07e-02 | 7.41e-01 |
| Trafficking of AMPA receptors | 29 | 4.52e-01 | 8.07e-02 | 7.41e-01 |
| Drug ADME | 97 | 1.70e-01 | 8.07e-02 | 4.48e-01 |
| SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 11 | 6.44e-01 | -8.05e-02 | 8.52e-01 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 103 | 1.59e-01 | 8.04e-02 | 4.30e-01 |
| Uptake and function of anthrax toxins | 11 | 6.44e-01 | -8.04e-02 | 8.52e-01 |
| RAB GEFs exchange GTP for GDP on RABs | 81 | 2.11e-01 | -8.03e-02 | 5.09e-01 |
| CLEC7A (Dectin-1) induces NFAT activation | 11 | 6.45e-01 | -8.03e-02 | 8.52e-01 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | 62 | 2.75e-01 | -8.02e-02 | 5.76e-01 |
| Endogenous sterols | 26 | 4.81e-01 | -7.99e-02 | 7.61e-01 |
| Initial triggering of complement | 21 | 5.26e-01 | -7.98e-02 | 7.81e-01 |
| Rab regulation of trafficking | 111 | 1.48e-01 | -7.95e-02 | 4.10e-01 |
| p75NTR regulates axonogenesis | 9 | 6.80e-01 | -7.95e-02 | 8.70e-01 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 14 | 6.08e-01 | -7.91e-02 | 8.27e-01 |
| MAPK1/MAPK3 signaling | 269 | 2.60e-02 | -7.89e-02 | 1.28e-01 |
| Digestion of dietary lipid | 7 | 7.18e-01 | 7.87e-02 | 8.96e-01 |
| Elastic fibre formation | 44 | 3.67e-01 | 7.87e-02 | 6.72e-01 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | 45 | 3.62e-01 | -7.86e-02 | 6.67e-01 |
| Defective CSF2RA causes SMDP4 | 7 | 7.20e-01 | -7.84e-02 | 8.96e-01 |
| Defective CSF2RB causes SMDP5 | 7 | 7.20e-01 | -7.84e-02 | 8.96e-01 |
| Transcriptional Regulation by TP53 | 351 | 1.17e-02 | -7.84e-02 | 7.01e-02 |
| Vitamin B2 (riboflavin) metabolism | 7 | 7.20e-01 | 7.82e-02 | 8.96e-01 |
| Neurexins and neuroligins | 52 | 3.30e-01 | 7.81e-02 | 6.33e-01 |
| Base-Excision Repair, AP Site Formation | 40 | 3.93e-01 | -7.80e-02 | 6.95e-01 |
| Phenylalanine metabolism | 6 | 7.41e-01 | -7.80e-02 | 9.07e-01 |
| Interleukin-23 signaling | 9 | 6.86e-01 | 7.79e-02 | 8.75e-01 |
| Organic cation transport | 10 | 6.70e-01 | 7.78e-02 | 8.64e-01 |
| EPH-Ephrin signaling | 90 | 2.02e-01 | -7.78e-02 | 4.95e-01 |
| Digestion | 17 | 5.80e-01 | 7.75e-02 | 8.17e-01 |
| Cellular Senescence | 159 | 9.19e-02 | -7.75e-02 | 3.08e-01 |
| Amyloid fiber formation | 73 | 2.53e-01 | 7.74e-02 | 5.56e-01 |
| Extra-nuclear estrogen signaling | 73 | 2.55e-01 | 7.70e-02 | 5.58e-01 |
| Glycosphingolipid biosynthesis | 19 | 5.61e-01 | 7.70e-02 | 8.08e-01 |
| Regulation of TP53 Activity through Acetylation | 28 | 4.81e-01 | -7.69e-02 | 7.61e-01 |
| Sema3A PAK dependent Axon repulsion | 14 | 6.18e-01 | -7.69e-02 | 8.30e-01 |
| DNA Damage/Telomere Stress Induced Senescence | 57 | 3.19e-01 | -7.64e-02 | 6.21e-01 |
| G alpha (z) signalling events | 48 | 3.60e-01 | 7.63e-02 | 6.67e-01 |
| Sodium/Proton exchangers | 7 | 7.27e-01 | 7.62e-02 | 9.02e-01 |
| RET signaling | 41 | 4.00e-01 | 7.60e-02 | 7.00e-01 |
| MicroRNA (miRNA) biogenesis | 26 | 5.02e-01 | -7.60e-02 | 7.66e-01 |
| Activation of GABAB receptors | 43 | 3.89e-01 | 7.60e-02 | 6.89e-01 |
| GABA B receptor activation | 43 | 3.89e-01 | 7.60e-02 | 6.89e-01 |
| DNA strand elongation | 31 | 4.64e-01 | -7.59e-02 | 7.52e-01 |
| Proton-coupled monocarboxylate transport | 6 | 7.48e-01 | 7.56e-02 | 9.10e-01 |
| Downregulation of ERBB2 signaling | 29 | 4.82e-01 | 7.53e-02 | 7.61e-01 |
| Adenylate cyclase activating pathway | 10 | 6.81e-01 | 7.51e-02 | 8.70e-01 |
| RAF/MAP kinase cascade | 263 | 3.63e-02 | -7.50e-02 | 1.64e-01 |
| SLC transporter disorders | 94 | 2.11e-01 | -7.47e-02 | 5.08e-01 |
| Dopamine Neurotransmitter Release Cycle | 21 | 5.54e-01 | 7.46e-02 | 8.02e-01 |
| Nef and signal transduction | 8 | 7.15e-01 | -7.46e-02 | 8.96e-01 |
| Elevation of cytosolic Ca2+ levels | 16 | 6.06e-01 | 7.45e-02 | 8.27e-01 |
| G beta:gamma signalling through PLC beta | 20 | 5.64e-01 | 7.45e-02 | 8.08e-01 |
| Nervous system development | 551 | 2.81e-03 | -7.45e-02 | 2.41e-02 |
| Protein methylation | 15 | 6.18e-01 | -7.44e-02 | 8.30e-01 |
| Glycosphingolipid transport | 8 | 7.16e-01 | -7.43e-02 | 8.96e-01 |
| Resolution of Abasic Sites (AP sites) | 38 | 4.29e-01 | -7.41e-02 | 7.25e-01 |
| Developmental Biology | 1194 | 1.68e-05 | 7.40e-02 | 4.74e-04 |
| Assembly Of The HIV Virion | 16 | 6.09e-01 | -7.39e-02 | 8.27e-01 |
| Molybdenum cofactor biosynthesis | 6 | 7.54e-01 | -7.38e-02 | 9.11e-01 |
| Signaling by FGFR2 in disease | 42 | 4.08e-01 | 7.37e-02 | 7.06e-01 |
| Defective CHST6 causes MCDC1 | 8 | 7.18e-01 | 7.36e-02 | 8.96e-01 |
| Base Excision Repair | 68 | 2.94e-01 | -7.36e-02 | 5.94e-01 |
| Maturation of spike protein 9683686 | 5 | 7.76e-01 | -7.36e-02 | 9.22e-01 |
| CDC42 GTPase cycle | 142 | 1.30e-01 | 7.36e-02 | 3.81e-01 |
| Collagen biosynthesis and modifying enzymes | 65 | 3.07e-01 | 7.32e-02 | 6.08e-01 |
| Downstream signal transduction | 29 | 4.96e-01 | -7.31e-02 | 7.64e-01 |
| Dectin-2 family | 28 | 5.04e-01 | -7.30e-02 | 7.68e-01 |
| PKA activation | 18 | 5.93e-01 | 7.28e-02 | 8.20e-01 |
| Muscle contraction | 196 | 7.90e-02 | 7.28e-02 | 2.78e-01 |
| Transcriptional Regulation by E2F6 | 32 | 4.77e-01 | -7.27e-02 | 7.61e-01 |
| Semaphorin interactions | 61 | 3.27e-01 | -7.26e-02 | 6.29e-01 |
| Respiratory syncytial virus (RSV) attachment and entry | 21 | 5.65e-01 | 7.26e-02 | 8.08e-01 |
| SUMO is proteolytically processed | 6 | 7.60e-01 | -7.22e-02 | 9.12e-01 |
| Smooth Muscle Contraction | 42 | 4.19e-01 | 7.21e-02 | 7.15e-01 |
| RAB geranylgeranylation | 57 | 3.48e-01 | -7.19e-02 | 6.54e-01 |
| TGF-beta receptor signaling activates SMADs | 47 | 3.94e-01 | -7.19e-02 | 6.95e-01 |
| Integration of energy metabolism | 105 | 2.03e-01 | 7.18e-02 | 4.95e-01 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 38 | 4.44e-01 | -7.18e-02 | 7.36e-01 |
| Regulation of CDH19 Expression and Function | 7 | 7.43e-01 | -7.16e-02 | 9.09e-01 |
| G beta:gamma signalling through CDC42 | 19 | 5.89e-01 | 7.16e-02 | 8.20e-01 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | 31 | 4.91e-01 | -7.15e-02 | 7.63e-01 |
| Nitric oxide stimulates guanylate cyclase | 21 | 5.71e-01 | 7.15e-02 | 8.13e-01 |
| RUNX3 regulates NOTCH signaling | 13 | 6.56e-01 | 7.14e-02 | 8.56e-01 |
| Platelet calcium homeostasis | 27 | 5.21e-01 | 7.13e-02 | 7.78e-01 |
| Striated Muscle Contraction | 35 | 4.66e-01 | 7.12e-02 | 7.52e-01 |
| Signaling by MET | 78 | 2.78e-01 | -7.11e-02 | 5.78e-01 |
| Transcriptional regulation by RUNX2 | 117 | 1.85e-01 | -7.10e-02 | 4.76e-01 |
| Listeria monocytogenes entry into host cells | 19 | 5.94e-01 | -7.07e-02 | 8.20e-01 |
| Advanced glycosylation endproduct receptor signaling | 13 | 6.60e-01 | -7.04e-02 | 8.59e-01 |
| Budding and maturation of HIV virion | 28 | 5.19e-01 | -7.04e-02 | 7.76e-01 |
| VEGFA-VEGFR2 Pathway | 94 | 2.38e-01 | -7.04e-02 | 5.44e-01 |
| Other semaphorin interactions | 18 | 6.07e-01 | -7.00e-02 | 8.27e-01 |
| Acyl chain remodelling of PG | 18 | 6.07e-01 | -7.00e-02 | 8.27e-01 |
| Positive epigenetic regulation of rRNA expression | 68 | 3.19e-01 | -6.99e-02 | 6.21e-01 |
| Role of LAT2/NTAL/LAB on calcium mobilization | 16 | 6.30e-01 | 6.95e-02 | 8.40e-01 |
| E2F mediated regulation of DNA replication | 20 | 5.91e-01 | -6.95e-02 | 8.20e-01 |
| Metabolism of proteins | 1899 | 5.50e-07 | -6.95e-02 | 1.96e-05 |
| Transcriptional Regulation by NPAS4 | 32 | 4.98e-01 | 6.92e-02 | 7.65e-01 |
| Gain-of-function MRAS complexes activate RAF signaling | 7 | 7.51e-01 | -6.92e-02 | 9.10e-01 |
| SHOC2 M1731 mutant abolishes MRAS complex function | 7 | 7.51e-01 | -6.92e-02 | 9.10e-01 |
| Signaling by MRAS-complex mutants | 7 | 7.51e-01 | -6.92e-02 | 9.10e-01 |
| Bacterial Infection Pathways | 67 | 3.28e-01 | -6.91e-02 | 6.31e-01 |
| NOTCH2 intracellular domain regulates transcription | 11 | 6.93e-01 | 6.89e-02 | 8.82e-01 |
| FCGR activation | 10 | 7.07e-01 | -6.87e-02 | 8.91e-01 |
| Generation of second messenger molecules | 25 | 5.53e-01 | 6.86e-02 | 8.02e-01 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 25 | 5.53e-01 | -6.85e-02 | 8.02e-01 |
| Pyruvate metabolism | 29 | 5.24e-01 | -6.83e-02 | 7.80e-01 |
| Intra-Golgi traffic | 43 | 4.39e-01 | -6.82e-02 | 7.32e-01 |
| EGFR downregulation | 29 | 5.26e-01 | 6.81e-02 | 7.81e-01 |
| Transport of RCbl within the body | 8 | 7.39e-01 | 6.81e-02 | 9.05e-01 |
| NOSTRIN mediated eNOS trafficking | 5 | 7.92e-01 | -6.80e-02 | 9.32e-01 |
| G alpha (12/13) signalling events | 74 | 3.12e-01 | 6.79e-02 | 6.15e-01 |
| Thrombin signalling through proteinase activated receptors (PARs) | 32 | 5.07e-01 | -6.77e-02 | 7.69e-01 |
| Defective pyroptosis | 34 | 4.95e-01 | -6.76e-02 | 7.64e-01 |
| Termination of translesion DNA synthesis | 32 | 5.09e-01 | -6.74e-02 | 7.70e-01 |
| LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production | 5 | 7.94e-01 | 6.73e-02 | 9.33e-01 |
| Death Receptor Signaling | 144 | 1.64e-01 | -6.72e-02 | 4.41e-01 |
| Transcription of the HIV genome | 66 | 3.45e-01 | -6.72e-02 | 6.53e-01 |
| Apoptotic execution phase | 49 | 4.19e-01 | -6.67e-02 | 7.15e-01 |
| NrCAM interactions | 6 | 7.77e-01 | -6.67e-02 | 9.23e-01 |
| Reduction of cytosolic Ca++ levels | 11 | 7.02e-01 | 6.65e-02 | 8.88e-01 |
| Acetylcholine regulates insulin secretion | 10 | 7.17e-01 | 6.63e-02 | 8.96e-01 |
| L1CAM interactions | 111 | 2.28e-01 | -6.62e-02 | 5.29e-01 |
| MET promotes cell motility | 41 | 4.65e-01 | -6.60e-02 | 7.52e-01 |
| Digestion of dietary carbohydrate | 6 | 7.80e-01 | 6.58e-02 | 9.23e-01 |
| Energy dependent regulation of mTOR by LKB1-AMPK | 28 | 5.49e-01 | 6.55e-02 | 7.98e-01 |
| EPHA-mediated growth cone collapse | 29 | 5.42e-01 | 6.54e-02 | 7.94e-01 |
| Autophagy | 142 | 1.79e-01 | -6.54e-02 | 4.64e-01 |
| Synthesis of diphthamide-EEF2 | 8 | 7.49e-01 | -6.54e-02 | 9.10e-01 |
| CD209 (DC-SIGN) signaling | 20 | 6.13e-01 | -6.53e-02 | 8.30e-01 |
| Signaling by VEGF | 102 | 2.55e-01 | -6.52e-02 | 5.58e-01 |
| Amino Acid conjugation | 8 | 7.50e-01 | 6.51e-02 | 9.10e-01 |
| Conjugation of carboxylic acids | 8 | 7.50e-01 | 6.51e-02 | 9.10e-01 |
| Activation of BH3-only proteins | 30 | 5.37e-01 | -6.51e-02 | 7.92e-01 |
| Macroautophagy | 128 | 2.04e-01 | -6.50e-02 | 4.95e-01 |
| Cytokine Signaling in Immune system | 713 | 3.19e-03 | -6.48e-02 | 2.68e-02 |
| Regulation of RUNX1 Expression and Activity | 25 | 5.75e-01 | 6.48e-02 | 8.15e-01 |
| Constitutive Signaling by EGFRvIII | 15 | 6.64e-01 | 6.47e-02 | 8.61e-01 |
| Signaling by EGFRvIII in Cancer | 15 | 6.64e-01 | 6.47e-02 | 8.61e-01 |
| Phase 2 - plateau phase | 14 | 6.75e-01 | -6.46e-02 | 8.65e-01 |
| ALK mutants bind TKIs | 12 | 6.98e-01 | -6.46e-02 | 8.86e-01 |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 17 | 6.47e-01 | 6.42e-02 | 8.53e-01 |
| TP53 Regulates Metabolic Genes | 83 | 3.13e-01 | -6.41e-02 | 6.15e-01 |
| Neddylation | 233 | 9.28e-02 | -6.39e-02 | 3.10e-01 |
| Highly calcium permeable nicotinic acetylcholine receptors | 9 | 7.40e-01 | 6.39e-02 | 9.06e-01 |
| G-protein beta:gamma signalling | 30 | 5.46e-01 | 6.37e-02 | 7.97e-01 |
| Regulation of TP53 Activity | 155 | 1.71e-01 | -6.37e-02 | 4.52e-01 |
| Hyaluronan metabolism | 17 | 6.50e-01 | -6.36e-02 | 8.53e-01 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 21 | 6.14e-01 | -6.36e-02 | 8.30e-01 |
| Visual phototransduction | 93 | 2.91e-01 | 6.34e-02 | 5.91e-01 |
| Transport of connexons to the plasma membrane | 19 | 6.32e-01 | 6.34e-02 | 8.42e-01 |
| Regulation of NPAS4 gene transcription | 5 | 8.06e-01 | -6.33e-02 | 9.42e-01 |
| Regulation of insulin secretion | 77 | 3.38e-01 | 6.31e-02 | 6.44e-01 |
| Aquaporin-mediated transport | 51 | 4.37e-01 | -6.28e-02 | 7.32e-01 |
| Miro GTPase Cycle | 8 | 7.58e-01 | -6.28e-02 | 9.12e-01 |
| Regulation of BACH1 activity | 15 | 6.75e-01 | 6.26e-02 | 8.65e-01 |
| Immune System | 1894 | 6.63e-06 | -6.26e-02 | 2.04e-04 |
| Metabolic disorders of biological oxidation enzymes | 32 | 5.41e-01 | 6.25e-02 | 7.93e-01 |
| Signaling by NOTCH3 | 48 | 4.54e-01 | 6.25e-02 | 7.42e-01 |
| Presynaptic function of Kainate receptors | 21 | 6.21e-01 | 6.23e-02 | 8.32e-01 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 16 | 6.67e-01 | 6.21e-02 | 8.63e-01 |
| Deadenylation of mRNA | 22 | 6.15e-01 | -6.20e-02 | 8.30e-01 |
| FLT3 signaling in disease | 28 | 5.72e-01 | -6.17e-02 | 8.14e-01 |
| HDL remodeling | 10 | 7.35e-01 | 6.17e-02 | 9.04e-01 |
| Respiratory Syncytial Virus Infection Pathway | 106 | 2.73e-01 | -6.16e-02 | 5.76e-01 |
| Glycosphingolipid catabolism | 33 | 5.41e-01 | -6.15e-02 | 7.93e-01 |
| Complement cascade | 54 | 4.35e-01 | -6.14e-02 | 7.30e-01 |
| Evasion by RSV of host interferon responses | 27 | 5.81e-01 | -6.13e-02 | 8.17e-01 |
| Organic anion transporters | 10 | 7.37e-01 | 6.12e-02 | 9.04e-01 |
| Pyrimidine catabolism | 12 | 7.14e-01 | -6.12e-02 | 8.96e-01 |
| Disease | 1689 | 3.00e-05 | -6.11e-02 | 7.80e-04 |
| Synthesis of IP2, IP, and Ins in the cytosol | 13 | 7.03e-01 | -6.10e-02 | 8.88e-01 |
| Gap junction trafficking | 46 | 4.75e-01 | 6.09e-02 | 7.61e-01 |
| Glycerophospholipid catabolism | 7 | 7.81e-01 | 6.08e-02 | 9.23e-01 |
| G beta:gamma signalling through BTK | 17 | 6.65e-01 | 6.07e-02 | 8.61e-01 |
| Azathioprine ADME | 19 | 6.48e-01 | -6.06e-02 | 8.53e-01 |
| CDC6 association with the ORC:origin complex | 8 | 7.67e-01 | 6.05e-02 | 9.16e-01 |
| IKK complex recruitment mediated by RIP1 | 22 | 6.24e-01 | -6.04e-02 | 8.34e-01 |
| RNA Polymerase I Transcription Initiation | 45 | 4.84e-01 | 6.03e-02 | 7.62e-01 |
| Processing of SMDT1 | 14 | 6.97e-01 | -6.02e-02 | 8.85e-01 |
| Antimicrobial peptides | 73 | 3.75e-01 | -6.01e-02 | 6.81e-01 |
| MET activates PI3K/AKT signaling | 6 | 7.99e-01 | 6.00e-02 | 9.37e-01 |
| PI3K/AKT Signaling in Cancer | 102 | 2.95e-01 | 6.00e-02 | 5.96e-01 |
| MAPK family signaling cascades | 310 | 7.02e-02 | -5.98e-02 | 2.56e-01 |
| Synthesis of PA | 37 | 5.30e-01 | 5.96e-02 | 7.85e-01 |
| Phase 3 - rapid repolarisation | 8 | 7.71e-01 | 5.96e-02 | 9.18e-01 |
| RHOG GTPase cycle | 71 | 3.87e-01 | 5.94e-02 | 6.89e-01 |
| Antigen processing: Ubiquitination & Proteasome degradation | 295 | 8.14e-02 | -5.90e-02 | 2.84e-01 |
| Cell-Cell communication | 148 | 2.16e-01 | 5.89e-02 | 5.15e-01 |
| Transport of inorganic cations/anions and amino acids/oligopeptides | 101 | 3.07e-01 | 5.89e-02 | 6.07e-01 |
| APEX1-Independent Resolution of AP Sites via the Single Nucleotide Replacement Pathway | 7 | 7.88e-01 | -5.88e-02 | 9.29e-01 |
| Glucagon signaling in metabolic regulation | 32 | 5.65e-01 | 5.88e-02 | 8.08e-01 |
| Vitamin D (calciferol) metabolism | 12 | 7.25e-01 | 5.88e-02 | 9.01e-01 |
| Synthesis of PIPs at the late endosome membrane | 10 | 7.48e-01 | -5.86e-02 | 9.10e-01 |
| Negative epigenetic regulation of rRNA expression | 70 | 3.99e-01 | -5.82e-02 | 7.00e-01 |
| rRNA processing in the mitochondrion | 9 | 7.62e-01 | -5.82e-02 | 9.14e-01 |
| NoRC negatively regulates rRNA expression | 68 | 4.08e-01 | -5.80e-02 | 7.06e-01 |
| Plasma lipoprotein clearance | 37 | 5.43e-01 | 5.78e-02 | 7.94e-01 |
| Signaling by NODAL | 20 | 6.55e-01 | -5.76e-02 | 8.56e-01 |
| Signaling by Nuclear Receptors | 259 | 1.11e-01 | 5.75e-02 | 3.46e-01 |
| Golgi Associated Vesicle Biogenesis | 51 | 4.77e-01 | -5.75e-02 | 7.61e-01 |
| Inositol phosphate metabolism | 45 | 5.07e-01 | -5.72e-02 | 7.69e-01 |
| Alpha-defensins | 8 | 7.81e-01 | -5.68e-02 | 9.23e-01 |
| RMTs methylate histone arginines | 43 | 5.19e-01 | 5.68e-02 | 7.76e-01 |
| Mitochondrial RNA degradation | 10 | 7.56e-01 | 5.67e-02 | 9.11e-01 |
| Gap junction trafficking and regulation | 48 | 4.97e-01 | 5.66e-02 | 7.65e-01 |
| PKMTs methylate histone lysines | 42 | 5.26e-01 | 5.66e-02 | 7.81e-01 |
| PCP/CE pathway | 91 | 3.52e-01 | -5.65e-02 | 6.59e-01 |
| SIRT1 negatively regulates rRNA expression | 30 | 5.94e-01 | -5.63e-02 | 8.20e-01 |
| RORA activates gene expression | 17 | 6.88e-01 | 5.62e-02 | 8.77e-01 |
| NF-kB is activated and signals survival | 12 | 7.36e-01 | -5.61e-02 | 9.04e-01 |
| Activated NTRK2 signals through CDK5 | 6 | 8.12e-01 | 5.61e-02 | 9.44e-01 |
| Mitochondrial iron-sulfur cluster biogenesis | 13 | 7.27e-01 | -5.60e-02 | 9.02e-01 |
| Formation of the beta-catenin:TCF transactivating complex | 55 | 4.75e-01 | 5.56e-02 | 7.61e-01 |
| Sulfur amino acid metabolism | 27 | 6.18e-01 | 5.55e-02 | 8.30e-01 |
| Cargo recognition for clathrin-mediated endocytosis | 99 | 3.41e-01 | 5.54e-02 | 6.46e-01 |
| Signaling by LRP5 mutants | 6 | 8.15e-01 | 5.53e-02 | 9.46e-01 |
| Bile acid and bile salt metabolism | 45 | 5.21e-01 | -5.53e-02 | 7.78e-01 |
| Metabolism | 2001 | 5.01e-05 | -5.49e-02 | 1.18e-03 |
| Regulation of TP53 Expression and Degradation | 37 | 5.64e-01 | -5.49e-02 | 8.08e-01 |
| FGFR2 mutant receptor activation | 32 | 5.92e-01 | 5.48e-02 | 8.20e-01 |
| Ion homeostasis | 52 | 4.95e-01 | -5.47e-02 | 7.64e-01 |
| SLBP independent Processing of Histone Pre-mRNAs | 10 | 7.65e-01 | -5.45e-02 | 9.16e-01 |
| Signal Transduction | 2466 | 1.01e-05 | 5.45e-02 | 3.01e-04 |
| Interferon gamma signaling | 86 | 3.83e-01 | 5.45e-02 | 6.85e-01 |
| Metabolism of water-soluble vitamins and cofactors | 125 | 2.95e-01 | -5.42e-02 | 5.96e-01 |
| Interaction With Cumulus Cells And The Zona Pellucida | 11 | 7.56e-01 | -5.41e-02 | 9.11e-01 |
| Epigenetic regulation of gene expression | 144 | 2.62e-01 | -5.41e-02 | 5.65e-01 |
| Defective CHST3 causes SEDCJD | 7 | 8.04e-01 | -5.40e-02 | 9.41e-01 |
| Modulation by Mtb of host immune system | 6 | 8.19e-01 | -5.39e-02 | 9.47e-01 |
| NFE2L2 regulating anti-oxidant/detoxification enzymes | 18 | 6.93e-01 | -5.38e-02 | 8.82e-01 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 59 | 4.75e-01 | 5.37e-02 | 7.61e-01 |
| Class I MHC mediated antigen processing & presentation | 359 | 8.23e-02 | -5.34e-02 | 2.87e-01 |
| FCERI mediated MAPK activation | 32 | 6.01e-01 | 5.34e-02 | 8.26e-01 |
| Basigin interactions | 24 | 6.51e-01 | 5.34e-02 | 8.53e-01 |
| RHOU GTPase cycle | 37 | 5.75e-01 | -5.33e-02 | 8.15e-01 |
| RHOB GTPase cycle | 66 | 4.54e-01 | 5.33e-02 | 7.42e-01 |
| Fatty acyl-CoA biosynthesis | 37 | 5.78e-01 | 5.28e-02 | 8.15e-01 |
| Paracetamol ADME | 26 | 6.41e-01 | 5.28e-02 | 8.50e-01 |
| Signaling by EGFR in Cancer | 24 | 6.54e-01 | 5.28e-02 | 8.55e-01 |
| Regulation of TP53 Degradation | 36 | 5.87e-01 | -5.23e-02 | 8.20e-01 |
| Synthesis of PIPs at the plasma membrane | 48 | 5.32e-01 | -5.22e-02 | 7.87e-01 |
| Signaling by Rho GTPases | 627 | 2.64e-02 | -5.19e-02 | 1.30e-01 |
| TP53 Regulates Transcription of Caspase Activators and Caspases | 12 | 7.55e-01 | 5.19e-02 | 9.11e-01 |
| Chromatin modifying enzymes | 216 | 1.88e-01 | -5.19e-02 | 4.78e-01 |
| Chromatin organization | 216 | 1.88e-01 | -5.19e-02 | 4.78e-01 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 119 | 3.29e-01 | -5.19e-02 | 6.31e-01 |
| Drug-mediated inhibition of CDK4/CDK6 activity | 5 | 8.41e-01 | -5.17e-02 | 9.53e-01 |
| Chylomicron clearance | 5 | 8.41e-01 | 5.17e-02 | 9.53e-01 |
| Adrenaline,noradrenaline inhibits insulin secretion | 28 | 6.36e-01 | 5.17e-02 | 8.45e-01 |
| Meiotic synapsis | 54 | 5.12e-01 | -5.15e-02 | 7.71e-01 |
| Netrin-1 signaling | 48 | 5.37e-01 | 5.15e-02 | 7.92e-01 |
| Signaling by Hedgehog | 147 | 2.81e-01 | -5.15e-02 | 5.82e-01 |
| HDACs deacetylate histones | 54 | 5.13e-01 | -5.15e-02 | 7.71e-01 |
| Diseases of carbohydrate metabolism | 31 | 6.20e-01 | -5.14e-02 | 8.31e-01 |
| Formation of the Early Elongation Complex | 32 | 6.15e-01 | -5.14e-02 | 8.30e-01 |
| Formation of the HIV-1 Early Elongation Complex | 32 | 6.15e-01 | -5.14e-02 | 8.30e-01 |
| MET activates PTPN11 | 5 | 8.44e-01 | 5.08e-02 | 9.53e-01 |
| LDL remodeling | 6 | 8.29e-01 | 5.08e-02 | 9.53e-01 |
| Signaling by NTRK1 (TRKA) | 113 | 3.51e-01 | -5.08e-02 | 6.59e-01 |
| PKA activation in glucagon signalling | 17 | 7.18e-01 | 5.05e-02 | 8.96e-01 |
| Adaptive Immune System | 721 | 2.09e-02 | -5.05e-02 | 1.12e-01 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 16 | 7.27e-01 | -5.05e-02 | 9.02e-01 |
| Translation of Replicase and Assembly of the Replication Transcription Complex 9694676 | 14 | 7.44e-01 | -5.05e-02 | 9.09e-01 |
| Neurofascin interactions | 6 | 8.32e-01 | 5.01e-02 | 9.53e-01 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 13 | 7.55e-01 | 5.01e-02 | 9.11e-01 |
| Tie2 Signaling | 18 | 7.13e-01 | -5.00e-02 | 8.96e-01 |
| RNA Polymerase I Promoter Opening | 26 | 6.59e-01 | -5.00e-02 | 8.59e-01 |
| A tetrasaccharide linker sequence is required for GAG synthesis | 23 | 6.78e-01 | 4.99e-02 | 8.69e-01 |
| HSF1-dependent transactivation | 34 | 6.16e-01 | 4.97e-02 | 8.30e-01 |
| OAS antiviral response | 8 | 8.09e-01 | -4.94e-02 | 9.42e-01 |
| Regulation of localization of FOXO transcription factors | 11 | 7.78e-01 | 4.92e-02 | 9.23e-01 |
| TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling | 11 | 7.78e-01 | -4.91e-02 | 9.23e-01 |
| Generic Transcription Pathway | 1181 | 4.69e-03 | 4.89e-02 | 3.46e-02 |
| Signaling by cytosolic FGFR1 fusion mutants | 18 | 7.20e-01 | -4.88e-02 | 8.96e-01 |
| Lysine catabolism | 12 | 7.70e-01 | -4.88e-02 | 9.18e-01 |
| Interleukin-36 pathway | 7 | 8.23e-01 | -4.87e-02 | 9.50e-01 |
| MET Receptor Activation | 6 | 8.37e-01 | 4.85e-02 | 9.53e-01 |
| Signaling by Rho GTPases, Miro GTPases and RHOBTB3 | 641 | 3.63e-02 | -4.85e-02 | 1.64e-01 |
| Maturation of nucleoprotein 9683610 | 11 | 7.81e-01 | 4.84e-02 | 9.23e-01 |
| BBSome-mediated cargo-targeting to cilium | 23 | 6.88e-01 | -4.84e-02 | 8.77e-01 |
| Zinc transporters | 15 | 7.46e-01 | -4.83e-02 | 9.10e-01 |
| Activated NTRK3 signals through PI3K | 6 | 8.39e-01 | 4.79e-02 | 9.53e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 14 | 7.56e-01 | -4.79e-02 | 9.11e-01 |
| Diseases of signal transduction by growth factor receptors and second messengers | 442 | 8.49e-02 | -4.78e-02 | 2.91e-01 |
| Transport of vitamins, nucleosides, and related molecules | 38 | 6.10e-01 | 4.78e-02 | 8.29e-01 |
| Signaling by NTRK3 (TRKC) | 17 | 7.35e-01 | 4.75e-02 | 9.04e-01 |
| RUNX1 regulates transcription of genes involved in BCR signaling | 6 | 8.41e-01 | 4.74e-02 | 9.53e-01 |
| Replacement of protamines by nucleosomes in the male pronucleus | 22 | 7.00e-01 | -4.74e-02 | 8.87e-01 |
| Cytosolic sulfonation of small molecules | 22 | 7.02e-01 | 4.71e-02 | 8.88e-01 |
| Interferon Signaling | 246 | 2.04e-01 | -4.70e-02 | 4.95e-01 |
| Defensins | 32 | 6.46e-01 | 4.69e-02 | 8.53e-01 |
| Vesicle-mediated transport | 641 | 4.46e-02 | -4.65e-02 | 1.87e-01 |
| Platelet degranulation | 115 | 3.93e-01 | -4.61e-02 | 6.95e-01 |
| Zinc influx into cells by the SLC39 gene family | 10 | 8.01e-01 | 4.61e-02 | 9.38e-01 |
| Signaling by FGFR1 in disease | 38 | 6.25e-01 | 4.59e-02 | 8.34e-01 |
| Negative regulation of FLT3 | 15 | 7.61e-01 | -4.54e-02 | 9.12e-01 |
| Estrogen-stimulated signaling through PRKCZ | 6 | 8.48e-01 | 4.53e-02 | 9.53e-01 |
| Regulated proteolysis of p75NTR | 11 | 7.95e-01 | -4.53e-02 | 9.33e-01 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | 54 | 5.66e-01 | -4.52e-02 | 8.08e-01 |
| Signaling by ERBB2 | 50 | 5.81e-01 | 4.51e-02 | 8.17e-01 |
| G beta:gamma signalling through PI3Kgamma | 25 | 6.97e-01 | 4.50e-02 | 8.85e-01 |
| RND2 GTPase cycle | 41 | 6.19e-01 | 4.49e-02 | 8.30e-01 |
| ATF6 (ATF6-alpha) activates chaperone genes | 10 | 8.06e-01 | 4.49e-02 | 9.41e-01 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 42 | 6.15e-01 | 4.49e-02 | 8.30e-01 |
| Oxidative Stress Induced Senescence | 88 | 4.68e-01 | -4.48e-02 | 7.54e-01 |
| Diseases of Base Excision Repair | 5 | 8.62e-01 | -4.48e-02 | 9.60e-01 |
| PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 | 9 | 8.17e-01 | -4.45e-02 | 9.47e-01 |
| Keratan sulfate degradation | 15 | 7.66e-01 | 4.43e-02 | 9.16e-01 |
| MET receptor recycling | 10 | 8.09e-01 | 4.41e-02 | 9.42e-01 |
| Membrane Trafficking | 603 | 6.47e-02 | -4.41e-02 | 2.43e-01 |
| Insulin processing | 24 | 7.10e-01 | 4.38e-02 | 8.94e-01 |
| NPAS4 regulates expression of target genes | 20 | 7.35e-01 | 4.37e-02 | 9.04e-01 |
| Transferrin endocytosis and recycling | 29 | 6.84e-01 | 4.37e-02 | 8.74e-01 |
| RAS signaling downstream of NF1 loss-of-function variants | 7 | 8.42e-01 | -4.36e-02 | 9.53e-01 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 30 | 6.80e-01 | 4.35e-02 | 8.70e-01 |
| Toll-like Receptor Cascades | 158 | 3.46e-01 | -4.34e-02 | 6.53e-01 |
| Regulation of Complement cascade | 43 | 6.24e-01 | -4.32e-02 | 8.34e-01 |
| Activation of NOXA and translocation to mitochondria | 5 | 8.67e-01 | 4.31e-02 | 9.63e-01 |
| STING mediated induction of host immune responses | 16 | 7.68e-01 | -4.27e-02 | 9.16e-01 |
| Signal amplification | 33 | 6.72e-01 | -4.27e-02 | 8.64e-01 |
| Defects in biotin (Btn) metabolism | 8 | 8.36e-01 | 4.22e-02 | 9.53e-01 |
| Pre-NOTCH Processing in Golgi | 18 | 7.57e-01 | 4.21e-02 | 9.12e-01 |
| Kinesins | 59 | 5.79e-01 | -4.18e-02 | 8.16e-01 |
| TRAF6 mediated IRF7 activation | 22 | 7.35e-01 | -4.17e-02 | 9.04e-01 |
| FCERI mediated Ca+2 mobilization | 30 | 6.95e-01 | 4.14e-02 | 8.84e-01 |
| Nuclear Receptor transcription pathway | 51 | 6.11e-01 | 4.12e-02 | 8.29e-01 |
| Glycerophospholipid biosynthesis | 122 | 4.32e-01 | -4.12e-02 | 7.27e-01 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 20 | 7.51e-01 | -4.09e-02 | 9.10e-01 |
| Activated NOTCH1 Transmits Signal to the Nucleus | 30 | 6.99e-01 | 4.08e-02 | 8.86e-01 |
| Sphingolipid de novo biosynthesis | 37 | 6.69e-01 | -4.06e-02 | 8.64e-01 |
| Activation of Ca-permeable Kainate Receptor | 9 | 8.33e-01 | -4.06e-02 | 9.53e-01 |
| Ionotropic activity of kainate receptors | 9 | 8.33e-01 | -4.06e-02 | 9.53e-01 |
| FOXO-mediated transcription of cell cycle genes | 16 | 7.79e-01 | -4.05e-02 | 9.23e-01 |
| Potential therapeutics for SARS | 92 | 5.04e-01 | -4.03e-02 | 7.68e-01 |
| Interleukin-1 processing | 9 | 8.34e-01 | 4.02e-02 | 9.53e-01 |
| HIV Transcription Initiation | 43 | 6.51e-01 | -3.99e-02 | 8.53e-01 |
| RNA Polymerase II HIV Promoter Escape | 43 | 6.51e-01 | -3.99e-02 | 8.53e-01 |
| RNA Polymerase II Promoter Escape | 43 | 6.51e-01 | -3.99e-02 | 8.53e-01 |
| RNA Polymerase II Transcription Initiation | 43 | 6.51e-01 | -3.99e-02 | 8.53e-01 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 43 | 6.51e-01 | -3.99e-02 | 8.53e-01 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 43 | 6.51e-01 | -3.99e-02 | 8.53e-01 |
| tRNA modification in the mitochondrion | 8 | 8.46e-01 | -3.98e-02 | 9.53e-01 |
| Chylomicron remodeling | 10 | 8.28e-01 | 3.97e-02 | 9.53e-01 |
| Response to elevated platelet cytosolic Ca2+ | 120 | 4.55e-01 | -3.94e-02 | 7.42e-01 |
| Diseases associated with glycosylation precursor biosynthesis | 15 | 7.92e-01 | -3.94e-02 | 9.32e-01 |
| Signaling by WNT | 288 | 2.50e-01 | 3.94e-02 | 5.55e-01 |
| PKA-mediated phosphorylation of CREB | 19 | 7.67e-01 | 3.93e-02 | 9.16e-01 |
| Activation of HOX genes during differentiation | 83 | 5.39e-01 | 3.90e-02 | 7.92e-01 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 83 | 5.39e-01 | 3.90e-02 | 7.92e-01 |
| NCAM signaling for neurite out-growth | 62 | 5.97e-01 | 3.88e-02 | 8.22e-01 |
| Activation of kainate receptors upon glutamate binding | 29 | 7.18e-01 | 3.88e-02 | 8.96e-01 |
| RND3 GTPase cycle | 41 | 6.68e-01 | 3.88e-02 | 8.63e-01 |
| RNA Polymerase I Transcription Termination | 29 | 7.19e-01 | 3.86e-02 | 8.96e-01 |
| Ca2+ activated K+ channels | 9 | 8.42e-01 | -3.84e-02 | 9.53e-01 |
| Regulation of FOXO transcriptional activity by acetylation | 9 | 8.42e-01 | 3.83e-02 | 9.53e-01 |
| Noncanonical activation of NOTCH3 | 8 | 8.52e-01 | -3.81e-02 | 9.56e-01 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | 18 | 7.80e-01 | 3.81e-02 | 9.23e-01 |
| N-glycan antennae elongation in the medial/trans-Golgi | 26 | 7.37e-01 | 3.81e-02 | 9.04e-01 |
| FLT3 signaling through SRC family kinases | 6 | 8.72e-01 | -3.79e-02 | 9.63e-01 |
| Metal ion SLC transporters | 23 | 7.53e-01 | -3.79e-02 | 9.11e-01 |
| Leishmania infection | 155 | 4.16e-01 | -3.78e-02 | 7.13e-01 |
| Parasitic Infection Pathways | 155 | 4.16e-01 | -3.78e-02 | 7.13e-01 |
| Beta-oxidation of very long chain fatty acids | 10 | 8.37e-01 | -3.77e-02 | 9.53e-01 |
| Small interfering RNA (siRNA) biogenesis | 9 | 8.45e-01 | 3.77e-02 | 9.53e-01 |
| ADP signalling through P2Y purinoceptor 1 | 25 | 7.45e-01 | -3.76e-02 | 9.10e-01 |
| CD163 mediating an anti-inflammatory response | 9 | 8.45e-01 | -3.75e-02 | 9.53e-01 |
| Adenylate cyclase inhibitory pathway | 14 | 8.08e-01 | 3.75e-02 | 9.42e-01 |
| Keratan sulfate/keratin metabolism | 36 | 6.98e-01 | 3.73e-02 | 8.86e-01 |
| Pyrimidine salvage | 10 | 8.39e-01 | -3.72e-02 | 9.53e-01 |
| Post-translational protein modification | 1341 | 2.28e-02 | -3.71e-02 | 1.18e-01 |
| SMAD2/3 Phosphorylation Motif Mutants in Cancer | 6 | 8.77e-01 | -3.66e-02 | 9.63e-01 |
| TGFBR1 KD Mutants in Cancer | 6 | 8.77e-01 | -3.66e-02 | 9.63e-01 |
| Opioid Signalling | 89 | 5.52e-01 | -3.64e-02 | 8.02e-01 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | 15 | 8.07e-01 | 3.64e-02 | 9.42e-01 |
| PTK6 Regulates Proteins Involved in RNA Processing | 5 | 8.89e-01 | 3.62e-02 | 9.67e-01 |
| Sperm Motility And Taxes | 9 | 8.52e-01 | -3.58e-02 | 9.56e-01 |
| Regulation of MECP2 expression and activity | 30 | 7.35e-01 | 3.57e-02 | 9.04e-01 |
| Phase I - Functionalization of compounds | 100 | 5.41e-01 | -3.54e-02 | 7.93e-01 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 38 | 7.07e-01 | -3.52e-02 | 8.91e-01 |
| Metabolism of steroids | 149 | 4.59e-01 | -3.52e-02 | 7.44e-01 |
| p75NTR recruits signalling complexes | 12 | 8.33e-01 | -3.51e-02 | 9.53e-01 |
| IRF3-mediated induction of type I IFN | 13 | 8.27e-01 | -3.50e-02 | 9.53e-01 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | 16 | 8.08e-01 | -3.50e-02 | 9.42e-01 |
| STAT5 activation downstream of FLT3 ITD mutants | 10 | 8.48e-01 | -3.49e-02 | 9.54e-01 |
| Integrin cell surface interactions | 83 | 5.83e-01 | 3.48e-02 | 8.18e-01 |
| Assembly of the ORC complex at the origin of replication | 32 | 7.33e-01 | -3.48e-02 | 9.04e-01 |
| GP1b-IX-V activation signalling | 11 | 8.42e-01 | 3.48e-02 | 9.53e-01 |
| RUNX3 regulates BCL2L11 (BIM) transcription | 5 | 8.94e-01 | 3.44e-02 | 9.67e-01 |
| Interleukin-4 and Interleukin-13 signaling | 103 | 5.46e-01 | -3.44e-02 | 7.97e-01 |
| SUMOylation | 170 | 4.40e-01 | -3.43e-02 | 7.32e-01 |
| Signaling by Non-Receptor Tyrosine Kinases | 54 | 6.64e-01 | -3.41e-02 | 8.61e-01 |
| Signaling by PTK6 | 54 | 6.64e-01 | -3.41e-02 | 8.61e-01 |
| Synthesis of bile acids and bile salts | 34 | 7.31e-01 | -3.40e-02 | 9.04e-01 |
| Synthesis of bile acids and bile salts via 24-hydroxycholesterol | 14 | 8.26e-01 | -3.39e-02 | 9.53e-01 |
| cGMP effects | 16 | 8.15e-01 | 3.38e-02 | 9.46e-01 |
| Signaling by FGFR2 | 72 | 6.20e-01 | -3.38e-02 | 8.31e-01 |
| Sphingolipid catabolism | 12 | 8.40e-01 | -3.37e-02 | 9.53e-01 |
| DAG and IP3 signaling | 40 | 7.12e-01 | 3.37e-02 | 8.96e-01 |
| Killing mechanisms | 11 | 8.47e-01 | 3.35e-02 | 9.53e-01 |
| WNT5:FZD7-mediated leishmania damping | 11 | 8.47e-01 | 3.35e-02 | 9.53e-01 |
| Free fatty acids regulate insulin secretion | 10 | 8.55e-01 | 3.34e-02 | 9.56e-01 |
| Histidine catabolism | 8 | 8.71e-01 | -3.31e-02 | 9.63e-01 |
| RND1 GTPase cycle | 41 | 7.14e-01 | 3.31e-02 | 8.96e-01 |
| Signaling by NOTCH1 | 69 | 6.35e-01 | 3.30e-02 | 8.44e-01 |
| Xenobiotics | 22 | 7.89e-01 | 3.30e-02 | 9.30e-01 |
| Keratan sulfate biosynthesis | 28 | 7.63e-01 | 3.29e-02 | 9.14e-01 |
| Phosphate bond hydrolysis by NTPDase proteins | 8 | 8.73e-01 | -3.28e-02 | 9.63e-01 |
| PTEN Regulation | 150 | 4.90e-01 | -3.27e-02 | 7.63e-01 |
| Regulation of NFE2L2 gene expression | 8 | 8.73e-01 | 3.26e-02 | 9.63e-01 |
| Synthesis of substrates in N-glycan biosythesis | 62 | 6.59e-01 | -3.24e-02 | 8.59e-01 |
| CD28 dependent Vav1 pathway | 11 | 8.53e-01 | 3.22e-02 | 9.56e-01 |
| Highly sodium permeable postsynaptic acetylcholine nicotinic receptors | 7 | 8.83e-01 | 3.21e-02 | 9.65e-01 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 25 | 7.82e-01 | -3.20e-02 | 9.23e-01 |
| G2 Phase | 5 | 9.01e-01 | -3.20e-02 | 9.72e-01 |
| RAC1 GTPase cycle | 171 | 4.74e-01 | 3.17e-02 | 7.61e-01 |
| Synthesis of 15-eicosatetraenoic acid derivatives | 6 | 8.93e-01 | -3.16e-02 | 9.67e-01 |
| MTOR signalling | 40 | 7.31e-01 | -3.14e-02 | 9.04e-01 |
| Synthesis of PI | 5 | 9.04e-01 | -3.10e-02 | 9.73e-01 |
| Glutathione synthesis and recycling | 12 | 8.54e-01 | -3.06e-02 | 9.56e-01 |
| HDL assembly | 8 | 8.82e-01 | 3.03e-02 | 9.65e-01 |
| Chaperone Mediated Autophagy | 20 | 8.15e-01 | -3.03e-02 | 9.46e-01 |
| Phospholipid metabolism | 199 | 4.63e-01 | -3.02e-02 | 7.50e-01 |
| Purine catabolism | 17 | 8.32e-01 | 2.97e-02 | 9.53e-01 |
| Fatty Acids bound to GPR40 (FFAR1) regulate insulin secretion | 8 | 8.85e-01 | -2.95e-02 | 9.66e-01 |
| RHOV GTPase cycle | 36 | 7.61e-01 | 2.93e-02 | 9.12e-01 |
| RHOC GTPase cycle | 70 | 6.72e-01 | -2.92e-02 | 8.65e-01 |
| FLT3 Signaling | 38 | 7.57e-01 | -2.90e-02 | 9.12e-01 |
| Nucleotide catabolism | 35 | 7.67e-01 | -2.89e-02 | 9.16e-01 |
| Metabolism of lipids | 723 | 1.86e-01 | -2.89e-02 | 4.78e-01 |
| Post-chaperonin tubulin folding pathway | 22 | 8.17e-01 | -2.85e-02 | 9.47e-01 |
| PECAM1 interactions | 12 | 8.66e-01 | -2.82e-02 | 9.62e-01 |
| Platelet activation, signaling and aggregation | 247 | 4.45e-01 | -2.82e-02 | 7.38e-01 |
| Glutamate Neurotransmitter Release Cycle | 24 | 8.11e-01 | 2.82e-02 | 9.44e-01 |
| Amino acid transport across the plasma membrane | 30 | 7.91e-01 | 2.80e-02 | 9.31e-01 |
| Effects of PIP2 hydrolysis | 26 | 8.05e-01 | -2.79e-02 | 9.41e-01 |
| Miscellaneous substrates | 12 | 8.68e-01 | -2.78e-02 | 9.63e-01 |
| FGFR2b ligand binding and activation | 10 | 8.80e-01 | 2.77e-02 | 9.64e-01 |
| COPI-independent Golgi-to-ER retrograde traffic | 51 | 7.33e-01 | -2.76e-02 | 9.04e-01 |
| Phase 1 - inactivation of fast Na+ channels | 6 | 9.07e-01 | 2.76e-02 | 9.73e-01 |
| RAC3 GTPase cycle | 85 | 6.63e-01 | 2.74e-02 | 8.61e-01 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | 12 | 8.70e-01 | -2.73e-02 | 9.63e-01 |
| Phase 0 - rapid depolarisation | 31 | 7.93e-01 | -2.72e-02 | 9.32e-01 |
| Acetylcholine binding and downstream events | 14 | 8.60e-01 | 2.72e-02 | 9.58e-01 |
| Postsynaptic nicotinic acetylcholine receptors | 14 | 8.60e-01 | 2.72e-02 | 9.58e-01 |
| Regulation of IFNG signaling | 14 | 8.61e-01 | 2.71e-02 | 9.58e-01 |
| VLDLR internalisation and degradation | 16 | 8.51e-01 | 2.71e-02 | 9.55e-01 |
| Signaling by PDGFRA extracellular domain mutants | 12 | 8.72e-01 | 2.69e-02 | 9.63e-01 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 12 | 8.72e-01 | 2.69e-02 | 9.63e-01 |
| PD-1 signaling | 17 | 8.48e-01 | 2.69e-02 | 9.53e-01 |
| Lysosome Vesicle Biogenesis | 33 | 7.89e-01 | -2.69e-02 | 9.30e-01 |
| Presynaptic depolarization and calcium channel opening | 12 | 8.72e-01 | -2.68e-02 | 9.63e-01 |
| RHOA GTPase cycle | 139 | 5.89e-01 | 2.65e-02 | 8.20e-01 |
| Metalloprotease DUBs | 27 | 8.12e-01 | -2.64e-02 | 9.44e-01 |
| Regulation of TP53 Activity through Methylation | 19 | 8.42e-01 | -2.63e-02 | 9.53e-01 |
| Signaling by NTRKs | 132 | 6.01e-01 | -2.63e-02 | 8.26e-01 |
| NFE2L2 regulates pentose phosphate pathway genes | 7 | 9.04e-01 | 2.63e-02 | 9.73e-01 |
| Cell surface interactions at the vascular wall | 123 | 6.16e-01 | -2.62e-02 | 8.30e-01 |
| Regulation of PTEN gene transcription | 59 | 7.28e-01 | -2.61e-02 | 9.02e-01 |
| Syndecan interactions | 26 | 8.18e-01 | 2.61e-02 | 9.47e-01 |
| Glycogen metabolism | 22 | 8.32e-01 | 2.61e-02 | 9.53e-01 |
| APOBEC3G mediated resistance to HIV-1 infection | 5 | 9.20e-01 | 2.60e-02 | 9.78e-01 |
| Diseases of glycosylation | 139 | 5.97e-01 | 2.60e-02 | 8.22e-01 |
| Dermatan sulfate biosynthesis | 10 | 8.87e-01 | 2.60e-02 | 9.67e-01 |
| Stimuli-sensing channels | 101 | 6.53e-01 | 2.59e-02 | 8.54e-01 |
| IRAK2 mediated activation of TAK1 complex | 9 | 8.93e-01 | -2.58e-02 | 9.67e-01 |
| NR1H2 & NR1H3 regulate gene expression linked to triglyceride lipolysis in adipose | 5 | 9.21e-01 | 2.56e-02 | 9.79e-01 |
| Signaling by FGFR in disease | 62 | 7.29e-01 | 2.55e-02 | 9.02e-01 |
| Translation of Replicase and Assembly of the Replication Transcription Complex 9679504 | 13 | 8.75e-01 | -2.53e-02 | 9.63e-01 |
| Synthesis of glycosylphosphatidylinositol (GPI) | 17 | 8.57e-01 | -2.53e-02 | 9.57e-01 |
| SUMO E3 ligases SUMOylate target proteins | 164 | 5.82e-01 | -2.49e-02 | 8.18e-01 |
| RNA Polymerase II Transcription | 1299 | 1.34e-01 | 2.48e-02 | 3.86e-01 |
| SLC-mediated transmembrane transport | 237 | 5.13e-01 | 2.47e-02 | 7.71e-01 |
| Sphingolipid metabolism | 101 | 6.70e-01 | -2.46e-02 | 8.64e-01 |
| Signaling by Receptor Tyrosine Kinases | 510 | 3.46e-01 | 2.44e-02 | 6.53e-01 |
| Cell death signalling via NRAGE, NRIF and NADE | 69 | 7.30e-01 | 2.40e-02 | 9.04e-01 |
| Aggrephagy | 40 | 7.94e-01 | 2.39e-02 | 9.32e-01 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 29 | 8.26e-01 | -2.36e-02 | 9.52e-01 |
| CREB1 phosphorylation through the activation of Adenylate Cyclase | 11 | 8.93e-01 | -2.35e-02 | 9.67e-01 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants | 15 | 8.75e-01 | 2.34e-02 | 9.63e-01 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer | 15 | 8.75e-01 | 2.34e-02 | 9.63e-01 |
| The phototransduction cascade | 32 | 8.19e-01 | -2.33e-02 | 9.47e-01 |
| Synthesis of PC | 27 | 8.34e-01 | -2.33e-02 | 9.53e-01 |
| Growth hormone receptor signaling | 22 | 8.50e-01 | 2.32e-02 | 9.55e-01 |
| Plasma lipoprotein assembly, remodeling, and clearance | 74 | 7.31e-01 | 2.31e-02 | 9.04e-01 |
| FBXW7 Mutants and NOTCH1 in Cancer | 5 | 9.29e-01 | 2.29e-02 | 9.80e-01 |
| Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling | 5 | 9.29e-01 | 2.29e-02 | 9.80e-01 |
| Signaling by FLT3 fusion proteins | 19 | 8.63e-01 | -2.29e-02 | 9.60e-01 |
| Multifunctional anion exchangers | 9 | 9.06e-01 | 2.28e-02 | 9.73e-01 |
| Regulation of lipid metabolism by PPARalpha | 115 | 6.74e-01 | -2.27e-02 | 8.65e-01 |
| Ion transport by P-type ATPases | 51 | 7.81e-01 | -2.25e-02 | 9.23e-01 |
| NOTCH1 Intracellular Domain Regulates Transcription | 44 | 8.01e-01 | 2.19e-02 | 9.39e-01 |
| Prostanoid ligand receptors | 9 | 9.09e-01 | -2.19e-02 | 9.74e-01 |
| Signaling by FLT3 ITD and TKD mutants | 16 | 8.81e-01 | -2.17e-02 | 9.65e-01 |
| RNA Polymerase I Promoter Escape | 53 | 7.86e-01 | -2.15e-02 | 9.28e-01 |
| Alpha-protein kinase 1 signaling pathway | 10 | 9.09e-01 | -2.10e-02 | 9.74e-01 |
| Metabolism of steroid hormones | 34 | 8.33e-01 | 2.09e-02 | 9.53e-01 |
| Synthesis of Dolichyl-phosphate | 6 | 9.30e-01 | -2.07e-02 | 9.80e-01 |
| Translation of Structural Proteins 9683701 | 29 | 8.47e-01 | -2.07e-02 | 9.53e-01 |
| HuR (ELAVL1) binds and stabilizes mRNA | 10 | 9.10e-01 | 2.06e-02 | 9.74e-01 |
| Late SARS-CoV-2 Infection Events | 67 | 7.71e-01 | 2.06e-02 | 9.18e-01 |
| Unwinding of DNA | 12 | 9.03e-01 | -2.04e-02 | 9.73e-01 |
| Signaling by PDGFR in disease | 20 | 8.76e-01 | 2.02e-02 | 9.63e-01 |
| Ovarian tumor domain proteases | 36 | 8.34e-01 | -2.02e-02 | 9.53e-01 |
| Ras activation upon Ca2+ influx through NMDA receptor | 19 | 8.79e-01 | 2.01e-02 | 9.64e-01 |
| Biological oxidations | 202 | 6.24e-01 | -2.00e-02 | 8.34e-01 |
| Platelet homeostasis | 84 | 7.56e-01 | 1.96e-02 | 9.11e-01 |
| InlB-mediated entry of Listeria monocytogenes into host cell | 14 | 8.99e-01 | -1.95e-02 | 9.71e-01 |
| Anti-inflammatory response favouring Leishmania parasite infection | 73 | 7.73e-01 | -1.95e-02 | 9.20e-01 |
| Leishmania parasite growth and survival | 73 | 7.73e-01 | -1.95e-02 | 9.20e-01 |
| Beta-oxidation of pristanoyl-CoA | 9 | 9.20e-01 | -1.94e-02 | 9.78e-01 |
| Interleukin-6 family signaling | 24 | 8.69e-01 | 1.94e-02 | 9.63e-01 |
| RSV-host interactions | 84 | 7.59e-01 | -1.94e-02 | 9.12e-01 |
| Negative regulation of TCF-dependent signaling by DVL-interacting proteins | 5 | 9.40e-01 | -1.94e-02 | 9.84e-01 |
| Clathrin-mediated endocytosis | 138 | 7.00e-01 | 1.90e-02 | 8.87e-01 |
| NGF-stimulated transcription | 38 | 8.40e-01 | 1.89e-02 | 9.53e-01 |
| ADP signalling through P2Y purinoceptor 12 | 22 | 8.79e-01 | 1.87e-02 | 9.64e-01 |
| ESR-mediated signaling | 182 | 6.67e-01 | 1.85e-02 | 8.63e-01 |
| Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) | 12 | 9.12e-01 | -1.84e-02 | 9.75e-01 |
| Activation of NMDA receptors and postsynaptic events | 86 | 7.69e-01 | 1.83e-02 | 9.17e-01 |
| PTK6 Regulates Cell Cycle | 6 | 9.38e-01 | 1.83e-02 | 9.83e-01 |
| Metabolism of carbohydrates | 283 | 5.98e-01 | -1.82e-02 | 8.23e-01 |
| Signaling by NOTCH | 205 | 6.58e-01 | -1.80e-02 | 8.58e-01 |
| mitochondrial fatty acid beta-oxidation of saturated fatty acids | 11 | 9.18e-01 | 1.80e-02 | 9.78e-01 |
| MET activates PTK2 signaling | 30 | 8.66e-01 | -1.78e-02 | 9.63e-01 |
| Ca-dependent events | 36 | 8.54e-01 | -1.77e-02 | 9.56e-01 |
| RUNX2 regulates bone development | 29 | 8.70e-01 | -1.76e-02 | 9.63e-01 |
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 24 | 8.83e-01 | -1.74e-02 | 9.65e-01 |
| Heme signaling | 45 | 8.44e-01 | -1.69e-02 | 9.53e-01 |
| G-protein mediated events | 53 | 8.32e-01 | -1.68e-02 | 9.53e-01 |
| Signaling by TGFB family members | 121 | 7.52e-01 | -1.67e-02 | 9.10e-01 |
| Activation of AMPK downstream of NMDARs | 27 | 8.81e-01 | -1.66e-02 | 9.65e-01 |
| Signaling by EGFR | 51 | 8.38e-01 | 1.65e-02 | 9.53e-01 |
| Conjugation of benzoate with glycine | 6 | 9.44e-01 | 1.65e-02 | 9.84e-01 |
| FOXO-mediated transcription | 65 | 8.19e-01 | -1.64e-02 | 9.47e-01 |
| TRAIL signaling | 8 | 9.36e-01 | 1.64e-02 | 9.83e-01 |
| PI Metabolism | 78 | 8.04e-01 | -1.63e-02 | 9.41e-01 |
| GRB7 events in ERBB2 signaling | 5 | 9.50e-01 | -1.62e-02 | 9.85e-01 |
| Synthesis of PIPs at the early endosome membrane | 15 | 9.14e-01 | -1.61e-02 | 9.76e-01 |
| Signaling by Hippo | 19 | 9.04e-01 | 1.61e-02 | 9.73e-01 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 22 | 8.97e-01 | 1.60e-02 | 9.69e-01 |
| RHOH GTPase cycle | 36 | 8.69e-01 | 1.59e-02 | 9.63e-01 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 14 | 9.18e-01 | -1.59e-02 | 9.78e-01 |
| Cell recruitment (pro-inflammatory response) | 26 | 8.89e-01 | -1.59e-02 | 9.67e-01 |
| Purinergic signaling in leishmaniasis infection | 26 | 8.89e-01 | -1.59e-02 | 9.67e-01 |
| TNFs bind their physiological receptors | 25 | 8.91e-01 | 1.59e-02 | 9.67e-01 |
| Iron uptake and transport | 56 | 8.39e-01 | -1.57e-02 | 9.53e-01 |
| GPVI-mediated activation cascade | 34 | 8.74e-01 | -1.57e-02 | 9.63e-01 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 19 | 9.06e-01 | 1.57e-02 | 9.73e-01 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 27 | 8.89e-01 | 1.55e-02 | 9.67e-01 |
| Platelet Aggregation (Plug Formation) | 39 | 8.70e-01 | -1.52e-02 | 9.63e-01 |
| Late endosomal microautophagy | 33 | 8.84e-01 | -1.47e-02 | 9.65e-01 |
| Defective CHSY1 causes TPBS | 7 | 9.47e-01 | -1.46e-02 | 9.84e-01 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 22 | 9.07e-01 | -1.44e-02 | 9.73e-01 |
| FGFR1 mutant receptor activation | 31 | 8.90e-01 | 1.44e-02 | 9.67e-01 |
| Inactivation, recovery and regulation of the phototransduction cascade | 31 | 8.90e-01 | -1.43e-02 | 9.67e-01 |
| Triglyceride metabolism | 34 | 8.86e-01 | 1.42e-02 | 9.67e-01 |
| Costimulation by the CD28 family | 61 | 8.49e-01 | -1.41e-02 | 9.54e-01 |
| p75 NTR receptor-mediated signalling | 90 | 8.19e-01 | -1.39e-02 | 9.47e-01 |
| LGI-ADAM interactions | 14 | 9.29e-01 | 1.38e-02 | 9.80e-01 |
| PI3K/AKT activation | 9 | 9.43e-01 | 1.38e-02 | 9.84e-01 |
| Uptake and actions of bacterial toxins | 28 | 8.99e-01 | -1.38e-02 | 9.71e-01 |
| Maturation of spike protein 9694548 | 35 | 8.88e-01 | 1.38e-02 | 9.67e-01 |
| Defective ST3GAL3 causes MCT12 and EIEE15 | 8 | 9.46e-01 | -1.37e-02 | 9.84e-01 |
| Nephrin family interactions | 21 | 9.14e-01 | 1.36e-02 | 9.76e-01 |
| Other interleukin signaling | 24 | 9.09e-01 | -1.35e-02 | 9.74e-01 |
| CD28 co-stimulation | 32 | 8.95e-01 | -1.34e-02 | 9.68e-01 |
| Synthesis of UDP-N-acetyl-glucosamine | 7 | 9.51e-01 | 1.34e-02 | 9.85e-01 |
| Metabolism of vitamins and cofactors | 188 | 7.51e-01 | -1.34e-02 | 9.10e-01 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | 11 | 9.39e-01 | 1.33e-02 | 9.83e-01 |
| ROBO receptors bind AKAP5 | 9 | 9.46e-01 | 1.30e-02 | 9.84e-01 |
| RUNX2 regulates osteoblast differentiation | 22 | 9.17e-01 | -1.29e-02 | 9.78e-01 |
| TCF dependent signaling in response to WNT | 192 | 7.60e-01 | 1.28e-02 | 9.12e-01 |
| PLC beta mediated events | 48 | 8.78e-01 | -1.28e-02 | 9.64e-01 |
| Signaling by KIT in disease | 20 | 9.22e-01 | -1.26e-02 | 9.79e-01 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 20 | 9.22e-01 | -1.26e-02 | 9.79e-01 |
| NFE2L2 regulating MDR associated enzymes | 8 | 9.51e-01 | 1.25e-02 | 9.85e-01 |
| Transport of small molecules | 704 | 5.73e-01 | -1.25e-02 | 8.15e-01 |
| E2F-enabled inhibition of pre-replication complex formation | 9 | 9.49e-01 | -1.24e-02 | 9.84e-01 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | 17 | 9.30e-01 | 1.23e-02 | 9.80e-01 |
| MHC class II antigen presentation | 117 | 8.21e-01 | 1.21e-02 | 9.48e-01 |
| Nucleotide-like (purinergic) receptors | 13 | 9.40e-01 | 1.20e-02 | 9.84e-01 |
| Ethanol oxidation | 12 | 9.43e-01 | 1.18e-02 | 9.84e-01 |
| Scavenging by Class A Receptors | 19 | 9.29e-01 | 1.18e-02 | 9.80e-01 |
| Signaling by Activin | 17 | 9.34e-01 | -1.17e-02 | 9.83e-01 |
| RAC2 GTPase cycle | 81 | 8.56e-01 | 1.16e-02 | 9.57e-01 |
| Transport of bile salts and organic acids, metal ions and amine compounds | 82 | 8.58e-01 | 1.14e-02 | 9.58e-01 |
| PPARA activates gene expression | 113 | 8.35e-01 | -1.14e-02 | 9.53e-01 |
| Myoclonic epilepsy of Lafora | 9 | 9.53e-01 | -1.12e-02 | 9.86e-01 |
| FCGR3A-mediated IL10 synthesis | 35 | 9.10e-01 | 1.11e-02 | 9.74e-01 |
| Glycosphingolipid metabolism | 52 | 8.92e-01 | -1.09e-02 | 9.67e-01 |
| Sialic acid metabolism | 33 | 9.16e-01 | 1.07e-02 | 9.77e-01 |
| Signaling by ALK | 27 | 9.24e-01 | -1.06e-02 | 9.80e-01 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 19 | 9.37e-01 | 1.04e-02 | 9.83e-01 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 19 | 9.37e-01 | 1.04e-02 | 9.83e-01 |
| GAB1 signalosome | 16 | 9.44e-01 | 1.01e-02 | 9.84e-01 |
| P2Y receptors | 9 | 9.60e-01 | 9.57e-03 | 9.89e-01 |
| Diseases associated with glycosaminoglycan metabolism | 38 | 9.19e-01 | 9.48e-03 | 9.78e-01 |
| Metabolism of nitric oxide: NOS3 activation and regulation | 14 | 9.51e-01 | 9.44e-03 | 9.85e-01 |
| Signaling by NOTCH2 | 32 | 9.28e-01 | 9.26e-03 | 9.80e-01 |
| Reactions specific to the complex N-glycan synthesis pathway | 10 | 9.60e-01 | -9.25e-03 | 9.89e-01 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 25 | 9.37e-01 | -9.15e-03 | 9.83e-01 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 10 | 9.60e-01 | -9.15e-03 | 9.89e-01 |
| EPH-ephrin mediated repulsion of cells | 50 | 9.12e-01 | 9.03e-03 | 9.75e-01 |
| Diseases associated with the TLR signaling cascade | 29 | 9.36e-01 | 8.59e-03 | 9.83e-01 |
| Diseases of Immune System | 29 | 9.36e-01 | 8.59e-03 | 9.83e-01 |
| G-protein activation | 24 | 9.43e-01 | -8.50e-03 | 9.84e-01 |
| Transcriptional regulation of white adipocyte differentiation | 81 | 8.95e-01 | 8.45e-03 | 9.68e-01 |
| TP53 Regulates Transcription of Cell Death Genes | 43 | 9.25e-01 | -8.33e-03 | 9.80e-01 |
| Phase II - Conjugation of compounds | 95 | 8.90e-01 | 8.24e-03 | 9.67e-01 |
| RNA Polymerase I Promoter Clearance | 71 | 9.05e-01 | 8.17e-03 | 9.73e-01 |
| RNA Polymerase I Transcription | 71 | 9.05e-01 | 8.17e-03 | 9.73e-01 |
| RHOT1 GTPase cycle | 5 | 9.75e-01 | 8.07e-03 | 9.99e-01 |
| Glucagon-type ligand receptors | 32 | 9.37e-01 | -8.02e-03 | 9.83e-01 |
| Hemostasis | 564 | 7.45e-01 | -8.02e-03 | 9.10e-01 |
| Synthesis of very long-chain fatty acyl-CoAs | 23 | 9.48e-01 | -7.87e-03 | 9.84e-01 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | 32 | 9.39e-01 | 7.84e-03 | 9.83e-01 |
| LDL clearance | 19 | 9.53e-01 | 7.76e-03 | 9.86e-01 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 28 | 9.43e-01 | -7.74e-03 | 9.84e-01 |
| SUMOylation of transcription cofactors | 44 | 9.30e-01 | 7.64e-03 | 9.80e-01 |
| Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 15 | 9.59e-01 | -7.59e-03 | 9.89e-01 |
| RUNX3 Regulates Immune Response and Cell Migration | 6 | 9.74e-01 | -7.59e-03 | 9.98e-01 |
| Defective B4GALT7 causes EDS, progeroid type | 17 | 9.57e-01 | 7.52e-03 | 9.89e-01 |
| Glutathione conjugation | 30 | 9.43e-01 | -7.50e-03 | 9.84e-01 |
| Defective B3GAT3 causes JDSSDHD | 17 | 9.59e-01 | -7.19e-03 | 9.89e-01 |
| Transcriptional regulation by RUNX1 | 204 | 8.60e-01 | 7.19e-03 | 9.58e-01 |
| Gene expression (Transcription) | 1463 | 6.49e-01 | 7.12e-03 | 8.53e-01 |
| Translation of Structural Proteins 9694635 | 55 | 9.29e-01 | -6.92e-03 | 9.80e-01 |
| Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) | 8 | 9.73e-01 | -6.80e-03 | 9.98e-01 |
| CaM pathway | 34 | 9.45e-01 | 6.78e-03 | 9.84e-01 |
| Calmodulin induced events | 34 | 9.45e-01 | 6.78e-03 | 9.84e-01 |
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 24 | 9.54e-01 | -6.74e-03 | 9.87e-01 |
| Signaling by FGFR | 87 | 9.16e-01 | 6.56e-03 | 9.77e-01 |
| Intracellular signaling by second messengers | 314 | 8.45e-01 | 6.44e-03 | 9.53e-01 |
| Cytochrome P450 - arranged by substrate type | 62 | 9.36e-01 | -5.90e-03 | 9.83e-01 |
| Synthesis of Lipoxins (LX) | 6 | 9.80e-01 | 5.81e-03 | 9.99e-01 |
| Uptake and function of diphtheria toxin | 6 | 9.81e-01 | 5.63e-03 | 9.99e-01 |
| ATF6 (ATF6-alpha) activates chaperones | 11 | 9.74e-01 | 5.61e-03 | 9.98e-01 |
| Common Pathway of Fibrin Clot Formation | 21 | 9.65e-01 | 5.55e-03 | 9.92e-01 |
| RHO GTPase cycle | 418 | 8.54e-01 | -5.25e-03 | 9.56e-01 |
| STAT5 Activation | 7 | 9.81e-01 | 5.18e-03 | 9.99e-01 |
| Transcriptional Regulation by VENTX | 41 | 9.59e-01 | -4.68e-03 | 9.89e-01 |
| Beta-catenin independent WNT signaling | 145 | 9.24e-01 | -4.58e-03 | 9.80e-01 |
| Thromboxane signalling through TP receptor | 24 | 9.70e-01 | 4.50e-03 | 9.96e-01 |
| Pyroptosis | 27 | 9.68e-01 | 4.49e-03 | 9.95e-01 |
| CD28 dependent PI3K/Akt signaling | 22 | 9.71e-01 | 4.42e-03 | 9.97e-01 |
| Oncogene Induced Senescence | 35 | 9.64e-01 | -4.40e-03 | 9.92e-01 |
| Carboxyterminal post-translational modifications of tubulin | 43 | 9.60e-01 | -4.38e-03 | 9.89e-01 |
| Factors involved in megakaryocyte development and platelet production | 143 | 9.28e-01 | -4.36e-03 | 9.80e-01 |
| Activation of IRF3, IRF7 mediated by TBK1, IKBKE | 17 | 9.76e-01 | 4.20e-03 | 9.99e-01 |
| Ion channel transport | 172 | 9.27e-01 | -4.03e-03 | 9.80e-01 |
| Maternal to zygotic transition (MZT) | 96 | 9.49e-01 | -3.77e-03 | 9.85e-01 |
| Estrogen-dependent gene expression | 113 | 9.46e-01 | -3.68e-03 | 9.84e-01 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 20 | 9.82e-01 | 2.92e-03 | 9.99e-01 |
| Cargo trafficking to the periciliary membrane | 49 | 9.73e-01 | -2.78e-03 | 9.98e-01 |
| Netrin mediated repulsion signals | 8 | 9.89e-01 | 2.69e-03 | 9.99e-01 |
| Heme degradation | 15 | 9.88e-01 | 2.22e-03 | 9.99e-01 |
| NRIF signals cell death from the nucleus | 16 | 9.89e-01 | 2.07e-03 | 9.99e-01 |
| Interleukin-15 signaling | 13 | 9.90e-01 | -1.92e-03 | 9.99e-01 |
| Prostacyclin signalling through prostacyclin receptor | 19 | 9.88e-01 | 1.91e-03 | 9.99e-01 |
| Circadian Clock | 66 | 9.80e-01 | 1.80e-03 | 9.99e-01 |
| Beta oxidation of hexanoyl-CoA to butanoyl-CoA | 5 | 9.95e-01 | 1.74e-03 | 9.99e-01 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | 30 | 9.87e-01 | -1.67e-03 | 9.99e-01 |
| Post NMDA receptor activation events | 75 | 9.81e-01 | 1.62e-03 | 9.99e-01 |
| Constitutive Signaling by Overexpressed ERBB2 | 11 | 9.93e-01 | -1.55e-03 | 9.99e-01 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 54 | 9.85e-01 | 1.51e-03 | 9.99e-01 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 54 | 9.85e-01 | 1.51e-03 | 9.99e-01 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 54 | 9.85e-01 | 1.51e-03 | 9.99e-01 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 54 | 9.85e-01 | 1.51e-03 | 9.99e-01 |
| Signaling by NOTCH1 in Cancer | 54 | 9.85e-01 | 1.51e-03 | 9.99e-01 |
| Suppression of apoptosis | 7 | 9.95e-01 | -1.45e-03 | 9.99e-01 |
| ADORA2B mediated anti-inflammatory cytokines production | 42 | 9.87e-01 | 1.45e-03 | 9.99e-01 |
| GPER1 signaling | 45 | 9.87e-01 | -1.41e-03 | 9.99e-01 |
| Signaling by ALK fusions and activated point mutants | 91 | 9.82e-01 | -1.36e-03 | 9.99e-01 |
| Signaling by ALK in cancer | 91 | 9.82e-01 | -1.36e-03 | 9.99e-01 |
| PRC2 methylates histones and DNA | 35 | 9.90e-01 | -1.27e-03 | 9.99e-01 |
| DNA methylation | 28 | 9.91e-01 | -1.25e-03 | 9.99e-01 |
| Role of phospholipids in phagocytosis | 23 | 9.92e-01 | -1.24e-03 | 9.99e-01 |
| Metabolism of Angiotensinogen to Angiotensins | 16 | 9.94e-01 | -1.13e-03 | 9.99e-01 |
| O-linked glycosylation of mucins | 62 | 9.89e-01 | -1.03e-03 | 9.99e-01 |
| Maturation of protein 3a 9683673 | 9 | 9.96e-01 | 9.56e-04 | 9.99e-01 |
| Maturation of protein 3a 9694719 | 9 | 9.96e-01 | 9.56e-04 | 9.99e-01 |
| Plasma lipoprotein remodeling | 33 | 9.93e-01 | -9.15e-04 | 9.99e-01 |
| Diseases of metabolism | 238 | 9.81e-01 | 8.99e-04 | 9.99e-01 |
| Transcriptional regulation of granulopoiesis | 53 | 9.91e-01 | 8.91e-04 | 9.99e-01 |
| Interleukin-21 signaling | 9 | 9.96e-01 | -8.84e-04 | 9.99e-01 |
| RUNX3 regulates YAP1-mediated transcription | 7 | 9.97e-01 | 7.27e-04 | 9.99e-01 |
| TLR3-mediated TICAM1-dependent programmed cell death | 6 | 9.98e-01 | -6.78e-04 | 9.99e-01 |
| Gastrin-CREB signalling pathway via PKC and MAPK | 17 | 9.96e-01 | 6.59e-04 | 9.99e-01 |
| Vasopressin regulates renal water homeostasis via Aquaporins | 42 | 9.95e-01 | 5.82e-04 | 9.99e-01 |
| Detoxification of Reactive Oxygen Species | 33 | 9.96e-01 | 4.77e-04 | 9.99e-01 |
| Maturation of nucleoprotein 9694631 | 15 | 9.98e-01 | 4.20e-04 | 9.99e-01 |
| PIP3 activates AKT signaling | 275 | 9.93e-01 | 3.02e-04 | 9.99e-01 |
| Glycogen synthesis | 13 | 9.99e-01 | 2.99e-04 | 1.00e+00 |
| Signaling by SCF-KIT | 42 | 9.97e-01 | 2.87e-04 | 9.99e-01 |
| rRNA modification in the mitochondrion | 6 | 1.00e+00 | -1.39e-04 | 1.00e+00 |
| Presynaptic nicotinic acetylcholine receptors | 12 | 1.00e+00 | 2.31e-05 | 1.00e+00 |
Regulation of gene expression in endocrine-committed (NEUROG3+) progenitor cells
| 1454 | |
|---|---|
| set | Regulation of gene expression in endocrine-committed (NEUROG3+) progenitor cells |
| setSize | 5 |
| pANOVA | 0.00176 |
| s.dist | 0.808 |
| p.adjustANOVA | 0.0171 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NEUROD1 | 7085 |
| NKX2-2 | 6613 |
| INSM1 | 6141 |
| PAX4 | 5984 |
| NEUROG3 | 2756 |
| GeneID | Gene Rank |
|---|---|
| NEUROD1 | 7085 |
| NKX2-2 | 6613 |
| INSM1 | 6141 |
| PAX4 | 5984 |
| NEUROG3 | 2756 |
Regulation of gene expression in early pancreatic precursor cells
| 1453 | |
|---|---|
| set | Regulation of gene expression in early pancreatic precursor cells |
| setSize | 8 |
| pANOVA | 0.000142 |
| s.dist | 0.777 |
| p.adjustANOVA | 0.00293 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PTF1A | 7682 |
| NKX6-1 | 7535 |
| PDX1 | 6909 |
| FGF10 | 6458 |
| ONECUT1 | 5952 |
| ONECUT3 | 4366 |
| HNF1B | 3754 |
| NR5A2 | 361 |
| GeneID | Gene Rank |
|---|---|
| PTF1A | 7682 |
| NKX6-1 | 7535 |
| PDX1 | 6909 |
| FGF10 | 6458 |
| ONECUT1 | 5952 |
| ONECUT3 | 4366 |
| HNF1B | 3754 |
| NR5A2 | 361 |
Formation of lateral plate mesoderm
| 594 | |
|---|---|
| set | Formation of lateral plate mesoderm |
| setSize | 5 |
| pANOVA | 0.00327 |
| s.dist | 0.76 |
| p.adjustANOVA | 0.027 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| BMP4 | 6828 |
| SHH | 5995 |
| IHH | 5840 |
| GATA4 | 5120 |
| FOXF1 | 2191 |
| GeneID | Gene Rank |
|---|---|
| BMP4 | 6828 |
| SHH | 5995 |
| IHH | 5840 |
| GATA4 | 5120 |
| FOXF1 | 2191 |
Free fatty acid receptors
| 609 | |
|---|---|
| set | Free fatty acid receptors |
| setSize | 5 |
| pANOVA | 0.00413 |
| s.dist | 0.74 |
| p.adjustANOVA | 0.0318 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GPR31 | 6524 |
| FFAR2 | 5963 |
| FFAR3 | 5673 |
| FFAR4 | 5654 |
| FFAR1 | 1130 |
| GeneID | Gene Rank |
|---|---|
| GPR31 | 6524 |
| FFAR2 | 5963 |
| FFAR3 | 5673 |
| FFAR4 | 5654 |
| FFAR1 | 1130 |
Formation of intermediate mesoderm
| 593 | |
|---|---|
| set | Formation of intermediate mesoderm |
| setSize | 8 |
| pANOVA | 0.00173 |
| s.dist | 0.639 |
| p.adjustANOVA | 0.0169 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| FOXC1 | 7512 |
| FOXC2 | 7449 |
| LHX1 | 6834 |
| BMP4 | 6828 |
| OSR1 | 5694 |
| FGF2 | 4461 |
| PAX2 | 1106 |
| PAX8 | -8720 |
| GeneID | Gene Rank |
|---|---|
| FOXC1 | 7512 |
| FOXC2 | 7449 |
| LHX1 | 6834 |
| BMP4 | 6828 |
| OSR1 | 5694 |
| FGF2 | 4461 |
| PAX2 | 1106 |
| PAX8 | -8720 |
Formation of the ureteric bud
| 605 | |
|---|---|
| set | Formation of the ureteric bud |
| setSize | 21 |
| pANOVA | 5.43e-07 |
| s.dist | 0.631 |
| p.adjustANOVA | 1.96e-05 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HOXD11 | 7607 |
| SALL1 | 7543 |
| FOXC1 | 7512 |
| FOXC2 | 7449 |
| GDNF | 7241 |
| SIX1 | 7238 |
| SIX2 | 7095 |
| GREM1 | 6900 |
| BMP4 | 6828 |
| HOXC11 | 6682 |
| SLIT2 | 5699 |
| GFRA1 | 5556 |
| NPNT | 4933 |
| HOXA11 | 4629 |
| EYA1 | 2632 |
| PAX2 | 1106 |
| ROBO2 | -559 |
| WNT11 | -857 |
| ITGB1 | -2169 |
| ITGA8 | -2572 |
| GeneID | Gene Rank |
|---|---|
| HOXD11 | 7607 |
| SALL1 | 7543 |
| FOXC1 | 7512 |
| FOXC2 | 7449 |
| GDNF | 7241 |
| SIX1 | 7238 |
| SIX2 | 7095 |
| GREM1 | 6900 |
| BMP4 | 6828 |
| HOXC11 | 6682 |
| SLIT2 | 5699 |
| GFRA1 | 5556 |
| NPNT | 4933 |
| HOXA11 | 4629 |
| EYA1 | 2632 |
| PAX2 | 1106 |
| ROBO2 | -559 |
| WNT11 | -857 |
| ITGB1 | -2169 |
| ITGA8 | -2572 |
| RET | -10592 |
Thyroxine biosynthesis
| 1824 | |
|---|---|
| set | Thyroxine biosynthesis |
| setSize | 10 |
| pANOVA | 0.000598 |
| s.dist | 0.627 |
| p.adjustANOVA | 0.00825 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DIO3 | 7712 |
| IYD | 7427 |
| TSHB | 6843 |
| TPO | 3986 |
| DUOX2 | 3967 |
| DIO1 | 3853 |
| SLC5A5 | 3741 |
| DUOX1 | 3573 |
| DIO2 | 26 |
| CGA | -3551 |
| GeneID | Gene Rank |
|---|---|
| DIO3 | 7712 |
| IYD | 7427 |
| TSHB | 6843 |
| TPO | 3986 |
| DUOX2 | 3967 |
| DIO1 | 3853 |
| SLC5A5 | 3741 |
| DUOX1 | 3573 |
| DIO2 | 26 |
| CGA | -3551 |
Transcriptional regulation of testis differentiation
| 1860 | |
|---|---|
| set | Transcriptional regulation of testis differentiation |
| setSize | 12 |
| pANOVA | 0.000205 |
| s.dist | 0.619 |
| p.adjustANOVA | 0.00397 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| FOXL2 | 7169 |
| SOX9 | 7018 |
| WT1 | 6994 |
| AMH | 5643 |
| ZFPM2 | 5392 |
| DHH | 5296 |
| GATA4 | 5120 |
| NR5A1 | 3821 |
| WNT4 | 2387 |
| DMRT1 | 598 |
| FGF9 | -758 |
| PTGDS | -4602 |
| GeneID | Gene Rank |
|---|---|
| FOXL2 | 7169 |
| SOX9 | 7018 |
| WT1 | 6994 |
| AMH | 5643 |
| ZFPM2 | 5392 |
| DHH | 5296 |
| GATA4 | 5120 |
| NR5A1 | 3821 |
| WNT4 | 2387 |
| DMRT1 | 598 |
| FGF9 | -758 |
| PTGDS | -4602 |
Acrosome Reaction and Sperm:Oocyte Membrane Binding
| 40 | |
|---|---|
| set | Acrosome Reaction and Sperm:Oocyte Membrane Binding |
| setSize | 6 |
| pANOVA | 0.0117 |
| s.dist | -0.594 |
| p.adjustANOVA | 0.0701 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IZUMO3 | -12485 |
| IZUMO4 | -12313 |
| CD9 | -12176 |
| ACR | -11794 |
| IZUMO2 | -8015 |
| IZUMO1 | 139 |
| GeneID | Gene Rank |
|---|---|
| IZUMO3 | -12485 |
| IZUMO4 | -12313 |
| CD9 | -12176 |
| ACR | -11794 |
| IZUMO2 | -8015 |
| IZUMO1 | 139 |
Electric Transmission Across Gap Junctions
| 500 | |
|---|---|
| set | Electric Transmission Across Gap Junctions |
| setSize | 5 |
| pANOVA | 0.0216 |
| s.dist | 0.593 |
| p.adjustANOVA | 0.114 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GJD2 | 7756 |
| PANX2 | 3732 |
| GJA10 | 2319 |
| PANX1 | 1878 |
| GJC1 | 1289 |
| GeneID | Gene Rank |
|---|---|
| GJD2 | 7756 |
| PANX2 | 3732 |
| GJA10 | 2319 |
| PANX1 | 1878 |
| GJC1 | 1289 |
Transmission across Electrical Synapses
| 1877 | |
|---|---|
| set | Transmission across Electrical Synapses |
| setSize | 5 |
| pANOVA | 0.0216 |
| s.dist | 0.593 |
| p.adjustANOVA | 0.114 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GJD2 | 7756 |
| PANX2 | 3732 |
| GJA10 | 2319 |
| PANX1 | 1878 |
| GJC1 | 1289 |
| GeneID | Gene Rank |
|---|---|
| GJD2 | 7756 |
| PANX2 | 3732 |
| GJA10 | 2319 |
| PANX1 | 1878 |
| GJC1 | 1289 |
Defective LFNG causes SCDO3
| 387 | |
|---|---|
| set | Defective LFNG causes SCDO3 |
| setSize | 5 |
| pANOVA | 0.0246 |
| s.dist | 0.58 |
| p.adjustANOVA | 0.125 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NOTCH2 | 5766 |
| NOTCH3 | 4610 |
| NOTCH1 | 4408 |
| NOTCH4 | 964 |
| LFNG | 535 |
| GeneID | Gene Rank |
|---|---|
| NOTCH2 | 5766 |
| NOTCH3 | 4610 |
| NOTCH1 | 4408 |
| NOTCH4 | 964 |
| LFNG | 535 |
Formation of the anterior neural plate
| 599 | |
|---|---|
| set | Formation of the anterior neural plate |
| setSize | 10 |
| pANOVA | 0.00179 |
| s.dist | 0.57 |
| p.adjustANOVA | 0.0171 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GBX2 | 7640 |
| SOX1 | 7384 |
| PAX6 | 6300 |
| OTX2 | 5859 |
| SOX2 | 5767 |
| ZIC2 | 5259 |
| NANOG | -15 |
| POU3F1 | -1529 |
| ZNF521 | -1750 |
| ZEB2 | -3454 |
| GeneID | Gene Rank |
|---|---|
| GBX2 | 7640 |
| SOX1 | 7384 |
| PAX6 | 6300 |
| OTX2 | 5859 |
| SOX2 | 5767 |
| ZIC2 | 5259 |
| NANOG | -15 |
| POU3F1 | -1529 |
| ZNF521 | -1750 |
| ZEB2 | -3454 |
Cobalamin (Cbl) metabolism
| 291 | |
|---|---|
| set | Cobalamin (Cbl) metabolism |
| setSize | 7 |
| pANOVA | 0.00939 |
| s.dist | -0.567 |
| p.adjustANOVA | 0.0602 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MMAB | -13141 |
| MMACHC | -11705 |
| MMADHC | -9728 |
| MTR | -8606 |
| MTRR | -8265 |
| MMAA | -7323 |
| MMUT | -5236 |
| GeneID | Gene Rank |
|---|---|
| MMAB | -13141 |
| MMACHC | -11705 |
| MMADHC | -9728 |
| MTR | -8606 |
| MTRR | -8265 |
| MMAA | -7323 |
| MMUT | -5236 |
Specification of the neural plate border
| 1703 | |
|---|---|
| set | Specification of the neural plate border |
| setSize | 16 |
| pANOVA | 9.64e-05 |
| s.dist | 0.563 |
| p.adjustANOVA | 0.0021 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GBX2 | 7640 |
| TFAP2C | 7521 |
| ZIC1 | 7144 |
| PAX3 | 7062 |
| BMP4 | 6828 |
| TFAP2A | 6066 |
| SOX2 | 5767 |
| DLX5 | 5470 |
| MSX1 | 5403 |
| FGF4 | 4269 |
| TFAP2B | 4229 |
| PAX7 | -480 |
| WNT3A | -2308 |
| CTNNB1 | -3925 |
| MYB | -4149 |
| TCF7L1 | -7472 |
| GeneID | Gene Rank |
|---|---|
| GBX2 | 7640 |
| TFAP2C | 7521 |
| ZIC1 | 7144 |
| PAX3 | 7062 |
| BMP4 | 6828 |
| TFAP2A | 6066 |
| SOX2 | 5767 |
| DLX5 | 5470 |
| MSX1 | 5403 |
| FGF4 | 4269 |
| TFAP2B | 4229 |
| PAX7 | -480 |
| WNT3A | -2308 |
| CTNNB1 | -3925 |
| MYB | -4149 |
| TCF7L1 | -7472 |
Hyaluronan biosynthesis and export
| 746 | |
|---|---|
| set | Hyaluronan biosynthesis and export |
| setSize | 5 |
| pANOVA | 0.031 |
| s.dist | 0.557 |
| p.adjustANOVA | 0.147 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HAS3 | 6591 |
| HAS2 | 5547 |
| HAS1 | 2881 |
| CEMIP | 846 |
| ABCC5 | -840 |
| GeneID | Gene Rank |
|---|---|
| HAS3 | 6591 |
| HAS2 | 5547 |
| HAS1 | 2881 |
| CEMIP | 846 |
| ABCC5 | -840 |
POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation
| 1166 | |
|---|---|
| set | POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation |
| setSize | 9 |
| pANOVA | 0.0044 |
| s.dist | 0.548 |
| p.adjustANOVA | 0.0333 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GSC | 7539 |
| HHEX | 7424 |
| DKK1 | 7070 |
| GATA6 | 6502 |
| CDX2 | 6281 |
| SOX2 | 5767 |
| NANOG | -15 |
| TSC22D1 | -3977 |
| EOMES | -10410 |
| GeneID | Gene Rank |
|---|---|
| GSC | 7539 |
| HHEX | 7424 |
| DKK1 | 7070 |
| GATA6 | 6502 |
| CDX2 | 6281 |
| SOX2 | 5767 |
| NANOG | -15 |
| TSC22D1 | -3977 |
| EOMES | -10410 |
Adrenoceptors
| 95 | |
|---|---|
| set | Adrenoceptors |
| setSize | 9 |
| pANOVA | 0.00443 |
| s.dist | 0.548 |
| p.adjustANOVA | 0.0334 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ADRA2C | 7213 |
| ADRB1 | 6159 |
| ADRA1A | 6076 |
| ADRA2B | 5991 |
| ADRA1B | 4915 |
| ADRA2A | 4291 |
| ADRB3 | 3583 |
| ADRA1D | -1153 |
| ADRB2 | -10943 |
| GeneID | Gene Rank |
|---|---|
| ADRA2C | 7213 |
| ADRB1 | 6159 |
| ADRA1A | 6076 |
| ADRA2B | 5991 |
| ADRA1B | 4915 |
| ADRA2A | 4291 |
| ADRB3 | 3583 |
| ADRA1D | -1153 |
| ADRB2 | -10943 |
Vasopressin-like receptors
| 1928 | |
|---|---|
| set | Vasopressin-like receptors |
| setSize | 5 |
| pANOVA | 0.0346 |
| s.dist | 0.546 |
| p.adjustANOVA | 0.159 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| AVPR1A | 7672 |
| AVPR1B | 6807 |
| AVP | 4139 |
| OXT | 1164 |
| OXTR | -5369 |
| GeneID | Gene Rank |
|---|---|
| AVPR1A | 7672 |
| AVPR1B | 6807 |
| AVP | 4139 |
| OXT | 1164 |
| OXTR | -5369 |
Kidney development
| 857 | |
|---|---|
| set | Kidney development |
| setSize | 45 |
| pANOVA | 2.62e-10 |
| s.dist | 0.544 |
| p.adjustANOVA | 2.52e-08 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IRX2 | 7751 |
| POU3F3 | 7673 |
| HOXD11 | 7607 |
| SALL1 | 7543 |
| IRX1 | 7534 |
| FOXC1 | 7512 |
| FOXC2 | 7449 |
| ID4 | 7372 |
| GDNF | 7241 |
| SIX1 | 7238 |
| SIX2 | 7095 |
| WT1 | 6994 |
| GREM1 | 6900 |
| EMX2 | 6889 |
| LHX1 | 6834 |
| BMP4 | 6828 |
| HOXC11 | 6682 |
| HOXA6 | 6608 |
| WNT9B | 6351 |
| SLIT2 | 5699 |
| GeneID | Gene Rank |
|---|---|
| IRX2 | 7751 |
| POU3F3 | 7673 |
| HOXD11 | 7607 |
| SALL1 | 7543 |
| IRX1 | 7534 |
| FOXC1 | 7512 |
| FOXC2 | 7449 |
| ID4 | 7372 |
| GDNF | 7241 |
| SIX1 | 7238 |
| SIX2 | 7095 |
| WT1 | 6994 |
| GREM1 | 6900 |
| EMX2 | 6889 |
| LHX1 | 6834 |
| BMP4 | 6828 |
| HOXC11 | 6682 |
| HOXA6 | 6608 |
| WNT9B | 6351 |
| SLIT2 | 5699 |
| OSR1 | 5694 |
| GFRA1 | 5556 |
| NPNT | 4933 |
| WFDC2 | 4815 |
| HOXA11 | 4629 |
| FGF2 | 4461 |
| HNF1B | 3754 |
| EYA1 | 2632 |
| WNT4 | 2387 |
| HOXB4 | 2134 |
| PAX2 | 1106 |
| LFNG | 535 |
| ROBO2 | -559 |
| PLAC8 | -593 |
| WNT11 | -857 |
| ITGB1 | -2169 |
| ITGA8 | -2572 |
| MECOM | -3193 |
| CTNNB1 | -3925 |
| DLL1 | -4687 |
| JAG1 | -5327 |
| GATA3 | -5746 |
| HNF4A | -6961 |
| PAX8 | -8720 |
| RET | -10592 |
CREB3 factors activate genes
| 210 | |
|---|---|
| set | CREB3 factors activate genes |
| setSize | 8 |
| pANOVA | 0.00862 |
| s.dist | -0.536 |
| p.adjustANOVA | 0.0565 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CREB3L1 | -11728 |
| CREB3L4 | -11262 |
| CREB3 | -10940 |
| CREBRF | -9733 |
| CREB3L3 | -8729 |
| DCSTAMP | -7935 |
| MBTPS1 | -7201 |
| CREB3L2 | -2969 |
| GeneID | Gene Rank |
|---|---|
| CREB3L1 | -11728 |
| CREB3L4 | -11262 |
| CREB3 | -10940 |
| CREBRF | -9733 |
| CREB3L3 | -8729 |
| DCSTAMP | -7935 |
| MBTPS1 | -7201 |
| CREB3L2 | -2969 |
Alpha-oxidation of phytanate
| 100 | |
|---|---|
| set | Alpha-oxidation of phytanate |
| setSize | 6 |
| pANOVA | 0.0232 |
| s.dist | -0.535 |
| p.adjustANOVA | 0.12 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PECR | -12033 |
| SLC27A2 | -12018 |
| SLC25A17 | -8858 |
| PHYH | -8684 |
| HACL1 | -7794 |
| ALDH3A2 | -3419 |
| GeneID | Gene Rank |
|---|---|
| PECR | -12033 |
| SLC27A2 | -12018 |
| SLC25A17 | -8858 |
| PHYH | -8684 |
| HACL1 | -7794 |
| ALDH3A2 | -3419 |
Dopamine receptors
| 455 | |
|---|---|
| set | Dopamine receptors |
| setSize | 5 |
| pANOVA | 0.0403 |
| s.dist | 0.53 |
| p.adjustANOVA | 0.174 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DRD5 | 7401 |
| DRD3 | 3753 |
| DRD1 | 2554 |
| DRD4 | 1745 |
| DRD2 | -1906 |
| GeneID | Gene Rank |
|---|---|
| DRD5 | 7401 |
| DRD3 | 3753 |
| DRD1 | 2554 |
| DRD4 | 1745 |
| DRD2 | -1906 |
Nephron development
| 1073 | |
|---|---|
| set | Nephron development |
| setSize | 13 |
| pANOVA | 0.00115 |
| s.dist | 0.521 |
| p.adjustANOVA | 0.0124 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IRX2 | 7751 |
| POU3F3 | 7673 |
| IRX1 | 7534 |
| WT1 | 6994 |
| LHX1 | 6834 |
| WNT9B | 6351 |
| HNF1B | 3754 |
| WNT4 | 2387 |
| PAX2 | 1106 |
| LFNG | 535 |
| DLL1 | -4687 |
| JAG1 | -5327 |
| HNF4A | -6961 |
| GeneID | Gene Rank |
|---|---|
| IRX2 | 7751 |
| POU3F3 | 7673 |
| IRX1 | 7534 |
| WT1 | 6994 |
| LHX1 | 6834 |
| WNT9B | 6351 |
| HNF1B | 3754 |
| WNT4 | 2387 |
| PAX2 | 1106 |
| LFNG | 535 |
| DLL1 | -4687 |
| JAG1 | -5327 |
| HNF4A | -6961 |
Neurotransmitter clearance
| 1082 | |
|---|---|
| set | Neurotransmitter clearance |
| setSize | 9 |
| pANOVA | 0.00857 |
| s.dist | 0.506 |
| p.adjustANOVA | 0.0565 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SLC22A1 | 6648 |
| ALDH2 | 5090 |
| SLC22A2 | 4871 |
| ACHE | 3665 |
| SLC6A3 | 3394 |
| COMT | 1884 |
| LRTOMT | 1086 |
| BCHE | 194 |
| SLC6A4 | -4755 |
| GeneID | Gene Rank |
|---|---|
| SLC22A1 | 6648 |
| ALDH2 | 5090 |
| SLC22A2 | 4871 |
| ACHE | 3665 |
| SLC6A3 | 3394 |
| COMT | 1884 |
| LRTOMT | 1086 |
| BCHE | 194 |
| SLC6A4 | -4755 |
Erythropoietin activates STAT5
| 515 | |
|---|---|
| set | Erythropoietin activates STAT5 |
| setSize | 7 |
| pANOVA | 0.0219 |
| s.dist | 0.5 |
| p.adjustANOVA | 0.114 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IRS2 | 7205 |
| EPO | 6777 |
| EPOR | 4419 |
| STAT5A | -39 |
| JAK2 | -279 |
| STAT5B | -648 |
| LYN | -687 |
| GeneID | Gene Rank |
|---|---|
| IRS2 | 7205 |
| EPO | 6777 |
| EPOR | 4419 |
| STAT5A | -39 |
| JAK2 | -279 |
| STAT5B | -648 |
| LYN | -687 |
Metal sequestration by antimicrobial proteins
| 958 | |
|---|---|
| set | Metal sequestration by antimicrobial proteins |
| setSize | 5 |
| pANOVA | 0.0541 |
| s.dist | -0.497 |
| p.adjustANOVA | 0.216 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| S100A7 | -13661 |
| LCN2 | -12365 |
| LTF | -11687 |
| S100A8 | -9998 |
| S100A9 | 5753 |
| GeneID | Gene Rank |
|---|---|
| S100A7 | -13661 |
| LCN2 | -12365 |
| LTF | -11687 |
| S100A8 | -9998 |
| S100A9 | 5753 |
Vitamins
| 1940 | |
|---|---|
| set | Vitamins |
| setSize | 6 |
| pANOVA | 0.0352 |
| s.dist | 0.497 |
| p.adjustANOVA | 0.161 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CYP26A1 | 6181 |
| CYP26B1 | 6122 |
| CYP26C1 | 5370 |
| CYP24A1 | 4765 |
| CYP27B1 | 4674 |
| CYP2R1 | -13006 |
| GeneID | Gene Rank |
|---|---|
| CYP26A1 | 6181 |
| CYP26B1 | 6122 |
| CYP26C1 | 5370 |
| CYP24A1 | 4765 |
| CYP27B1 | 4674 |
| CYP2R1 | -13006 |
Negative regulation of activity of TFAP2 (AP-2) family transcription factors
| 1069 | |
|---|---|
| set | Negative regulation of activity of TFAP2 (AP-2) family transcription factors |
| setSize | 10 |
| pANOVA | 0.00759 |
| s.dist | 0.487 |
| p.adjustANOVA | 0.0512 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TFAP2C | 7521 |
| TFAP2D | 6094 |
| TFAP2A | 6066 |
| TFAP2B | 4229 |
| KCTD15 | 4180 |
| TFAP2E | 2219 |
| UBE2I | 839 |
| WWOX | -407 |
| KCTD1 | -3032 |
| SUMO1 | -5183 |
| GeneID | Gene Rank |
|---|---|
| TFAP2C | 7521 |
| TFAP2D | 6094 |
| TFAP2A | 6066 |
| TFAP2B | 4229 |
| KCTD15 | 4180 |
| TFAP2E | 2219 |
| UBE2I | 839 |
| WWOX | -407 |
| KCTD1 | -3032 |
| SUMO1 | -5183 |
Prednisone ADME
| 1242 | |
|---|---|
| set | Prednisone ADME |
| setSize | 9 |
| pANOVA | 0.0124 |
| s.dist | 0.481 |
| p.adjustANOVA | 0.0727 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| AKR1C1 | 6441 |
| CYP3A4 | 4425 |
| ABCB1 | 4148 |
| UGT2B7 | 2887 |
| HSD11B1 | 2702 |
| ALB | 2367 |
| SERPINA6 | 1971 |
| HSD11B2 | -1399 |
| UGT1A3 | -3863 |
| GeneID | Gene Rank |
|---|---|
| AKR1C1 | 6441 |
| CYP3A4 | 4425 |
| ABCB1 | 4148 |
| UGT2B7 | 2887 |
| HSD11B1 | 2702 |
| ALB | 2367 |
| SERPINA6 | 1971 |
| HSD11B2 | -1399 |
| UGT1A3 | -3863 |
Signaling by RNF43 mutants
| 1669 | |
|---|---|
| set | Signaling by RNF43 mutants |
| setSize | 8 |
| pANOVA | 0.0196 |
| s.dist | 0.476 |
| p.adjustANOVA | 0.106 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| FZD8 | 7698 |
| FZD6 | 6503 |
| FZD4 | 1915 |
| LRP5 | 1122 |
| LRP6 | 1052 |
| RNF43 | 929 |
| FZD5 | 163 |
| WNT3A | -2308 |
| GeneID | Gene Rank |
|---|---|
| FZD8 | 7698 |
| FZD6 | 6503 |
| FZD4 | 1915 |
| LRP5 | 1122 |
| LRP6 | 1052 |
| RNF43 | 929 |
| FZD5 | 163 |
| WNT3A | -2308 |
Recycling of eIF2:GDP
| 1394 | |
|---|---|
| set | Recycling of eIF2:GDP |
| setSize | 7 |
| pANOVA | 0.0293 |
| s.dist | -0.476 |
| p.adjustANOVA | 0.142 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| EIF2B4 | -12225 |
| EIF2B1 | -11315 |
| EIF2S2 | -9683 |
| EIF2B5 | -9281 |
| EIF2B2 | -7948 |
| EIF2B3 | -3448 |
| EIF2S1 | -3192 |
| GeneID | Gene Rank |
|---|---|
| EIF2B4 | -12225 |
| EIF2B1 | -11315 |
| EIF2S2 | -9683 |
| EIF2B5 | -9281 |
| EIF2B2 | -7948 |
| EIF2B3 | -3448 |
| EIF2S1 | -3192 |
Sensing of DNA Double Strand Breaks
| 1578 | |
|---|---|
| set | Sensing of DNA Double Strand Breaks |
| setSize | 6 |
| pANOVA | 0.0448 |
| s.dist | -0.473 |
| p.adjustANOVA | 0.187 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KPNA2 | -12010 |
| KAT5 | -9796 |
| NBN | -8681 |
| RAD50 | -8372 |
| ATM | -5027 |
| MRE11 | -4883 |
| GeneID | Gene Rank |
|---|---|
| KPNA2 | -12010 |
| KAT5 | -9796 |
| NBN | -8681 |
| RAD50 | -8372 |
| ATM | -5027 |
| MRE11 | -4883 |
Organic anion transport
| 1128 | |
|---|---|
| set | Organic anion transport |
| setSize | 5 |
| pANOVA | 0.0693 |
| s.dist | -0.469 |
| p.adjustANOVA | 0.255 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SLC22A7 | -11885 |
| SLC22A6 | -11455 |
| SLC22A8 | -10549 |
| SLC22A12 | -3638 |
| SLC22A11 | -2902 |
| GeneID | Gene Rank |
|---|---|
| SLC22A7 | -11885 |
| SLC22A6 | -11455 |
| SLC22A8 | -10549 |
| SLC22A12 | -3638 |
| SLC22A11 | -2902 |
Ligand-receptor interactions
| 878 | |
|---|---|
| set | Ligand-receptor interactions |
| setSize | 8 |
| pANOVA | 0.0237 |
| s.dist | 0.462 |
| p.adjustANOVA | 0.122 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SHH | 5995 |
| IHH | 5840 |
| DHH | 5296 |
| HHIP | 3520 |
| GAS1 | 2312 |
| PTCH1 | 1814 |
| BOC | 103 |
| CDON | -9075 |
| GeneID | Gene Rank |
|---|---|
| SHH | 5995 |
| IHH | 5840 |
| DHH | 5296 |
| HHIP | 3520 |
| GAS1 | 2312 |
| PTCH1 | 1814 |
| BOC | 103 |
| CDON | -9075 |
Defective F9 activation
| 380 | |
|---|---|
| set | Defective F9 activation |
| setSize | 5 |
| pANOVA | 0.0782 |
| s.dist | 0.455 |
| p.adjustANOVA | 0.277 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GP1BA | 5489 |
| GP1BB | 4989 |
| GP5 | 4726 |
| F11 | -195 |
| GP9 | -5510 |
| GeneID | Gene Rank |
|---|---|
| GP1BA | 5489 |
| GP1BB | 4989 |
| GP5 | 4726 |
| F11 | -195 |
| GP9 | -5510 |
Establishment of Sister Chromatid Cohesion
| 516 | |
|---|---|
| set | Establishment of Sister Chromatid Cohesion |
| setSize | 9 |
| pANOVA | 0.0193 |
| s.dist | -0.45 |
| p.adjustANOVA | 0.105 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SMC3 | -12847 |
| CDCA5 | -11540 |
| ESCO1 | -9473 |
| PDS5B | -9133 |
| RAD21 | -8276 |
| WAPL | -6014 |
| ESCO2 | -5754 |
| PDS5A | -4655 |
| STAG1 | -3268 |
| GeneID | Gene Rank |
|---|---|
| SMC3 | -12847 |
| CDCA5 | -11540 |
| ESCO1 | -9473 |
| PDS5B | -9133 |
| RAD21 | -8276 |
| WAPL | -6014 |
| ESCO2 | -5754 |
| PDS5A | -4655 |
| STAG1 | -3268 |
Activation of TRKA receptors
| 73 | |
|---|---|
| set | Activation of TRKA receptors |
| setSize | 6 |
| pANOVA | 0.058 |
| s.dist | 0.447 |
| p.adjustANOVA | 0.225 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ADCYAP1 | 6673 |
| NGF | 5472 |
| NTRK2 | 4541 |
| ADCYAP1R1 | 1920 |
| ADORA2A | -1611 |
| NTRK1 | -6109 |
| GeneID | Gene Rank |
|---|---|
| ADCYAP1 | 6673 |
| NGF | 5472 |
| NTRK2 | 4541 |
| ADCYAP1R1 | 1920 |
| ADORA2A | -1611 |
| NTRK1 | -6109 |
Calcitonin-like ligand receptors
| 225 | |
|---|---|
| set | Calcitonin-like ligand receptors |
| setSize | 10 |
| pANOVA | 0.015 |
| s.dist | 0.444 |
| p.adjustANOVA | 0.0859 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IAPP | 7097 |
| CALCB | 4835 |
| RAMP2 | 4816 |
| CALCR | 2692 |
| CALCA | 2540 |
| RAMP1 | 1570 |
| ADM | 827 |
| CALCRL | 411 |
| ADM2 | -2571 |
| RAMP3 | -4348 |
| GeneID | Gene Rank |
|---|---|
| IAPP | 7097 |
| CALCB | 4835 |
| RAMP2 | 4816 |
| CALCR | 2692 |
| CALCA | 2540 |
| RAMP1 | 1570 |
| ADM | 827 |
| CALCRL | 411 |
| ADM2 | -2571 |
| RAMP3 | -4348 |
Folding of actin by CCT/TriC
| 578 | |
|---|---|
| set | Folding of actin by CCT/TriC |
| setSize | 10 |
| pANOVA | 0.0157 |
| s.dist | -0.441 |
| p.adjustANOVA | 0.0882 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ACTB | -12523.0 |
| CCT6A | -12153.0 |
| CCT5 | -10296.0 |
| CCT3 | -9342.0 |
| CCT7 | -8556.0 |
| CCT8 | -8305.0 |
| CCT6B | -8181.5 |
| CCT2 | -6944.0 |
| CCT4 | -1631.0 |
| TCP1 | 75.0 |
| GeneID | Gene Rank |
|---|---|
| ACTB | -12523.0 |
| CCT6A | -12153.0 |
| CCT5 | -10296.0 |
| CCT3 | -9342.0 |
| CCT7 | -8556.0 |
| CCT8 | -8305.0 |
| CCT6B | -8181.5 |
| CCT2 | -6944.0 |
| CCT4 | -1631.0 |
| TCP1 | 75.0 |
RUNX1 regulates transcription of genes involved in WNT signaling
| 1365 | |
|---|---|
| set | RUNX1 regulates transcription of genes involved in WNT signaling |
| setSize | 5 |
| pANOVA | 0.0892 |
| s.dist | 0.439 |
| p.adjustANOVA | 0.302 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RSPO3 | 5684 |
| ESR1 | 3251 |
| AXIN1 | 3158 |
| CBFB | -493 |
| RUNX1 | -2954 |
| GeneID | Gene Rank |
|---|---|
| RSPO3 | 5684 |
| ESR1 | 3251 |
| AXIN1 | 3158 |
| CBFB | -493 |
| RUNX1 | -2954 |
Tandem pore domain potassium channels
| 1804 | |
|---|---|
| set | Tandem pore domain potassium channels |
| setSize | 12 |
| pANOVA | 0.0101 |
| s.dist | 0.429 |
| p.adjustANOVA | 0.0631 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KCNK1 | 7359 |
| KCNK17 | 6912 |
| KCNK2 | 5866 |
| KCNK10 | 4130 |
| KCNK4 | 4051 |
| KCNK3 | 3012 |
| KCNK16 | 2436 |
| KCNK6 | -390 |
| KCNK7 | -2031 |
| KCNK9 | -3113 |
| KCNK13 | -3985 |
| KCNK18 | -4809 |
| GeneID | Gene Rank |
|---|---|
| KCNK1 | 7359 |
| KCNK17 | 6912 |
| KCNK2 | 5866 |
| KCNK10 | 4130 |
| KCNK4 | 4051 |
| KCNK3 | 3012 |
| KCNK16 | 2436 |
| KCNK6 | -390 |
| KCNK7 | -2031 |
| KCNK9 | -3113 |
| KCNK13 | -3985 |
| KCNK18 | -4809 |
CD22 mediated BCR regulation
| 190 | |
|---|---|
| set | CD22 mediated BCR regulation |
| setSize | 5 |
| pANOVA | 0.0981 |
| s.dist | 0.427 |
| p.adjustANOVA | 0.32 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CD79B | 5404 |
| CD79A | 5204 |
| PTPN6 | 2317 |
| LYN | -687 |
| CD22 | -4233 |
| GeneID | Gene Rank |
|---|---|
| CD79B | 5404 |
| CD79A | 5204 |
| PTPN6 | 2317 |
| LYN | -687 |
| CD22 | -4233 |
Mitotic Telophase/Cytokinesis
| 993 | |
|---|---|
| set | Mitotic Telophase/Cytokinesis |
| setSize | 11 |
| pANOVA | 0.0158 |
| s.dist | -0.42 |
| p.adjustANOVA | 0.0882 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SMC3 | -12847 |
| PDS5B | -9133 |
| PLK1 | -8560 |
| RAD21 | -8276 |
| MAU2 | -7982 |
| KIF23 | -7928 |
| NIPBL | -7444 |
| KIF20A | -7046 |
| WAPL | -6014 |
| PDS5A | -4655 |
| STAG1 | -3268 |
| GeneID | Gene Rank |
|---|---|
| SMC3 | -12847 |
| PDS5B | -9133 |
| PLK1 | -8560 |
| RAD21 | -8276 |
| MAU2 | -7982 |
| KIF23 | -7928 |
| NIPBL | -7444 |
| KIF20A | -7046 |
| WAPL | -6014 |
| PDS5A | -4655 |
| STAG1 | -3268 |
Phosphorylation of Emi1
| 1210 | |
|---|---|
| set | Phosphorylation of Emi1 |
| setSize | 6 |
| pANOVA | 0.0761 |
| s.dist | -0.418 |
| p.adjustANOVA | 0.272 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CDC20 | -12514 |
| CDK1 | -11603 |
| PLK1 | -8560 |
| CCNB1 | -5456 |
| FBXO5 | -5339 |
| FZR1 | -1747 |
| GeneID | Gene Rank |
|---|---|
| CDC20 | -12514 |
| CDK1 | -11603 |
| PLK1 | -8560 |
| CCNB1 | -5456 |
| FBXO5 | -5339 |
| FZR1 | -1747 |
SRP-dependent cotranslational protein targeting to membrane
| 1543 | |
|---|---|
| set | SRP-dependent cotranslational protein targeting to membrane |
| setSize | 105 |
| pANOVA | 1.29e-13 |
| s.dist | -0.418 |
| p.adjustANOVA | 2.58e-11 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS28 | -13541 |
| RPS11 | -13428 |
| SEC61G | -13400 |
| SPCS2 | -12999 |
| SPCS1 | -12994 |
| RPLP1 | -12918 |
| RPS14 | -12770 |
| RPL13 | -12670 |
| RPL12 | -12650 |
| RPL10A | -12605 |
| RPS6 | -12572 |
| FAU | -12534 |
| SRP9 | -12498 |
| SEC11C | -12481 |
| RPL29 | -12480 |
| RPL6 | -12413 |
| RPS21 | -12316 |
| RPL39L | -11987 |
| RPL27A | -11974 |
| RPS7 | -11943 |
| GeneID | Gene Rank |
|---|---|
| RPS28 | -13541.0 |
| RPS11 | -13428.0 |
| SEC61G | -13400.0 |
| SPCS2 | -12999.0 |
| SPCS1 | -12994.0 |
| RPLP1 | -12918.0 |
| RPS14 | -12770.0 |
| RPL13 | -12670.0 |
| RPL12 | -12650.0 |
| RPL10A | -12605.0 |
| RPS6 | -12572.0 |
| FAU | -12534.0 |
| SRP9 | -12498.0 |
| SEC11C | -12481.0 |
| RPL29 | -12480.0 |
| RPL6 | -12413.0 |
| RPS21 | -12316.0 |
| RPL39L | -11987.0 |
| RPL27A | -11974.0 |
| RPS7 | -11943.0 |
| SEC61B | -11605.0 |
| RPL8 | -11489.0 |
| RPS8 | -11311.0 |
| RPL37 | -11305.0 |
| SPCS3 | -11213.0 |
| RPLP0 | -11116.0 |
| RPL26 | -10923.0 |
| RPL7A | -10757.0 |
| RPL15 | -10752.0 |
| SRP72 | -10600.0 |
| RPS15A | -10582.0 |
| SRP19 | -10542.0 |
| SRPRB | -10480.0 |
| RPS29 | -10460.0 |
| UBA52 | -10435.0 |
| RPS10 | -10322.0 |
| RPLP2 | -10184.0 |
| RPL35 | -10155.0 |
| RPS25 | -10059.0 |
| RPN1 | -9916.0 |
| RPL11 | -9397.0 |
| RPS13 | -9323.0 |
| RPL28 | -9178.0 |
| RPL24 | -9053.0 |
| RPS12 | -8926.0 |
| SSR1 | -8917.0 |
| SRPRA | -8469.0 |
| RPS15 | -8457.0 |
| SRP54 | -8306.0 |
| RPS19 | -8292.0 |
| RPS20 | -8288.0 |
| RPL14 | -8223.0 |
| RPL36 | -8172.0 |
| RPL23A | -8167.0 |
| RPL38 | -7923.0 |
| DDOST | -7877.0 |
| RPL36AL | -7843.5 |
| RPL22L1 | -7745.0 |
| RPL7 | -7726.0 |
| RPL5 | -7632.0 |
| RPL37A | -7492.0 |
| RPS27L | -7459.0 |
| RPN2 | -7281.0 |
| RPL3L | -7129.0 |
| RPL3 | -6892.0 |
| SEC61A1 | -6817.0 |
| RPL18 | -6805.0 |
| RPL13A | -6656.5 |
| SSR3 | -6411.0 |
| SEC61A2 | -6408.0 |
| RPS5 | -6402.0 |
| SEC11A | -6169.0 |
| SRP68 | -6160.0 |
| SRP14 | -5864.0 |
| RPS2 | -5663.0 |
| RPSA | -5606.0 |
| RPL30 | -5110.0 |
| RPS18 | -4888.0 |
| RPL32 | -4258.0 |
| RPL23 | -4078.0 |
| RPS3A | -3946.0 |
| RPL9 | -3912.0 |
| RPL17 | -3404.0 |
| RPS24 | -3309.0 |
| RPL35A | -3266.0 |
| RPS3 | -2565.0 |
| RPL4 | -2514.0 |
| RPS23 | -2118.0 |
| RPL34 | -2114.0 |
| RPL27 | -1911.0 |
| RPS27 | -1878.0 |
| TRAM1 | -1798.0 |
| RPL21 | -1456.0 |
| RPL26L1 | -1390.0 |
| RPL31 | -1289.0 |
| RPS26 | -979.0 |
| SSR2 | -967.0 |
| RPL22 | -935.0 |
| RPL18A | -912.0 |
| RPS27A | -676.0 |
| RPL41 | -432.0 |
| RPS9 | 351.0 |
| RPL19 | 638.0 |
| RPS16 | 4527.0 |
| RPL10L | 6016.0 |
Formation of the nephric duct
| 602 | |
|---|---|
| set | Formation of the nephric duct |
| setSize | 17 |
| pANOVA | 0.00307 |
| s.dist | 0.415 |
| p.adjustANOVA | 0.026 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ID4 | 7372 |
| EMX2 | 6889 |
| LHX1 | 6834 |
| BMP4 | 6828 |
| HOXA6 | 6608 |
| OSR1 | 5694 |
| NPNT | 4933 |
| WFDC2 | 4815 |
| FGF2 | 4461 |
| HOXB4 | 2134 |
| PAX2 | 1106 |
| PLAC8 | -593 |
| MECOM | -3193 |
| CTNNB1 | -3925 |
| GATA3 | -5746 |
| PAX8 | -8720 |
| RET | -10592 |
| GeneID | Gene Rank |
|---|---|
| ID4 | 7372 |
| EMX2 | 6889 |
| LHX1 | 6834 |
| BMP4 | 6828 |
| HOXA6 | 6608 |
| OSR1 | 5694 |
| NPNT | 4933 |
| WFDC2 | 4815 |
| FGF2 | 4461 |
| HOXB4 | 2134 |
| PAX2 | 1106 |
| PLAC8 | -593 |
| MECOM | -3193 |
| CTNNB1 | -3925 |
| GATA3 | -5746 |
| PAX8 | -8720 |
| RET | -10592 |
Cellular response to mitochondrial stress
| 257 | |
|---|---|
| set | Cellular response to mitochondrial stress |
| setSize | 8 |
| pANOVA | 0.0424 |
| s.dist | -0.414 |
| p.adjustANOVA | 0.18 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DELE1 | -11224 |
| EIF2S2 | -9683 |
| YME1L1 | -9495 |
| PHB2 | -8690 |
| EIF2AK1 | -7118 |
| STOML2 | -6184 |
| OMA1 | -4374 |
| EIF2S1 | -3192 |
| GeneID | Gene Rank |
|---|---|
| DELE1 | -11224 |
| EIF2S2 | -9683 |
| YME1L1 | -9495 |
| PHB2 | -8690 |
| EIF2AK1 | -7118 |
| STOML2 | -6184 |
| OMA1 | -4374 |
| EIF2S1 | -3192 |
Formation of xylulose-5-phosphate
| 607 | |
|---|---|
| set | Formation of xylulose-5-phosphate |
| setSize | 5 |
| pANOVA | 0.109 |
| s.dist | -0.414 |
| p.adjustANOVA | 0.343 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DCXR | -12435 |
| AKR1A1 | -10988 |
| SORD | -10276 |
| CRYL1 | -3142 |
| XYLB | -598 |
| GeneID | Gene Rank |
|---|---|
| DCXR | -12435 |
| AKR1A1 | -10988 |
| SORD | -10276 |
| CRYL1 | -3142 |
| XYLB | -598 |
Cohesin Loading onto Chromatin
| 294 | |
|---|---|
| set | Cohesin Loading onto Chromatin |
| setSize | 8 |
| pANOVA | 0.0444 |
| s.dist | -0.41 |
| p.adjustANOVA | 0.187 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SMC3 | -12847 |
| PDS5B | -9133 |
| RAD21 | -8276 |
| MAU2 | -7982 |
| NIPBL | -7444 |
| WAPL | -6014 |
| PDS5A | -4655 |
| STAG1 | -3268 |
| GeneID | Gene Rank |
|---|---|
| SMC3 | -12847 |
| PDS5B | -9133 |
| RAD21 | -8276 |
| MAU2 | -7982 |
| NIPBL | -7444 |
| WAPL | -6014 |
| PDS5A | -4655 |
| STAG1 | -3268 |
Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.3.2 (2023-10-31)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 22.04.3 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.10.0
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.10.0
##
## 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
##
## time zone: Australia/Melbourne
## tzcode source: system (glibc)
##
## attached base packages:
## [1] parallel stats4 stats graphics grDevices utils datasets
## [8] methods base
##
## other attached packages:
## [1] pkgload_1.3.3
## [2] GGally_2.2.0
## [3] ggplot2_3.4.4
## [4] reshape2_1.4.4
## [5] gplots_3.1.3
## [6] gtools_3.9.5
## [7] tibble_3.2.1
## [8] dplyr_1.1.4
## [9] echarts4r_0.4.5
## [10] png_0.1-8
## [11] gridExtra_2.3
## [12] missMethyl_1.36.0
## [13] IlluminaHumanMethylation450kanno.ilmn12.hg19_0.6.1
## [14] beeswarm_0.4.0
## [15] kableExtra_1.3.4
## [16] mitch_1.15.0
## [17] tictoc_1.2
## [18] HGNChelper_0.8.1
## [19] IlluminaHumanMethylationEPICanno.ilm10b4.hg19_0.6.0
## [20] IlluminaHumanMethylation450kmanifest_0.4.0
## [21] minfi_1.48.0
## [22] bumphunter_1.44.0
## [23] locfit_1.5-9.8
## [24] iterators_1.0.14
## [25] foreach_1.5.2
## [26] Biostrings_2.70.1
## [27] XVector_0.42.0
## [28] SummarizedExperiment_1.32.0
## [29] Biobase_2.62.0
## [30] MatrixGenerics_1.14.0
## [31] matrixStats_1.2.0
## [32] GenomicRanges_1.54.1
## [33] GenomeInfoDb_1.38.1
## [34] IRanges_2.36.0
## [35] S4Vectors_0.40.1
## [36] BiocGenerics_0.48.1
## [37] eulerr_7.0.0
## [38] limma_3.58.1
##
## loaded via a namespace (and not attached):
## [1] splines_4.3.2 later_1.3.2
## [3] BiocIO_1.12.0 bitops_1.0-7
## [5] filelock_1.0.3 preprocessCore_1.64.0
## [7] XML_3.99-0.16 lifecycle_1.0.4
## [9] lattice_0.22-5 MASS_7.3-60
## [11] base64_2.0.1 scrime_1.3.5
## [13] magrittr_2.0.3 sass_0.4.8
## [15] rmarkdown_2.25 jquerylib_0.1.4
## [17] yaml_2.3.8 httpuv_1.6.13
## [19] doRNG_1.8.6 askpass_1.2.0
## [21] DBI_1.2.0 RColorBrewer_1.1-3
## [23] abind_1.4-5 zlibbioc_1.48.0
## [25] rvest_1.0.3 quadprog_1.5-8
## [27] purrr_1.0.2 RCurl_1.98-1.13
## [29] rappdirs_0.3.3 GenomeInfoDbData_1.2.11
## [31] genefilter_1.84.0 annotate_1.80.0
## [33] svglite_2.1.3 DelayedMatrixStats_1.24.0
## [35] codetools_0.2-19 DelayedArray_0.28.0
## [37] xml2_1.3.6 tidyselect_1.2.0
## [39] beanplot_1.3.1 BiocFileCache_2.10.1
## [41] webshot_0.5.5 illuminaio_0.44.0
## [43] GenomicAlignments_1.38.0 jsonlite_1.8.8
## [45] multtest_2.58.0 ellipsis_0.3.2
## [47] survival_3.5-7 systemfonts_1.0.5
## [49] tools_4.3.2 progress_1.2.3
## [51] Rcpp_1.0.11 glue_1.6.2
## [53] SparseArray_1.2.2 xfun_0.41
## [55] HDF5Array_1.30.0 withr_2.5.2
## [57] fastmap_1.1.1 rhdf5filters_1.14.1
## [59] fansi_1.0.6 openssl_2.1.1
## [61] caTools_1.18.2 digest_0.6.33
## [63] R6_2.5.1 mime_0.12
## [65] colorspace_2.1-0 biomaRt_2.58.0
## [67] RSQLite_2.3.4 utf8_1.2.4
## [69] tidyr_1.3.0 generics_0.1.3
## [71] data.table_1.14.10 rtracklayer_1.62.0
## [73] prettyunits_1.2.0 httr_1.4.7
## [75] htmlwidgets_1.6.4 S4Arrays_1.2.0
## [77] ggstats_0.5.1 pkgconfig_2.0.3
## [79] gtable_0.3.4 blob_1.2.4
## [81] siggenes_1.76.0 htmltools_0.5.7
## [83] scales_1.3.0 rstudioapi_0.15.0
## [85] knitr_1.45 tzdb_0.4.0
## [87] rjson_0.2.21 nlme_3.1-164
## [89] curl_5.2.0 org.Hs.eg.db_3.18.0
## [91] cachem_1.0.8 rhdf5_2.46.0
## [93] stringr_1.5.1 KernSmooth_2.23-22
## [95] AnnotationDbi_1.64.1 restfulr_0.0.15
## [97] GEOquery_2.70.0 pillar_1.9.0
## [99] grid_4.3.2 reshape_0.8.9
## [101] vctrs_0.6.5 promises_1.2.1
## [103] dbplyr_2.4.0 xtable_1.8-4
## [105] evaluate_0.23 readr_2.1.4
## [107] GenomicFeatures_1.54.1 cli_3.6.2
## [109] compiler_4.3.2 Rsamtools_2.18.0
## [111] rlang_1.1.2 crayon_1.5.2
## [113] rngtools_1.5.2 nor1mix_1.3-2
## [115] mclust_6.0.1 plyr_1.8.9
## [117] stringi_1.8.3 viridisLite_0.4.2
## [119] BiocParallel_1.36.0 munsell_0.5.0
## [121] Matrix_1.6-4 hms_1.1.3
## [123] sparseMatrixStats_1.14.0 bit64_4.0.5
## [125] Rhdf5lib_1.24.0 KEGGREST_1.42.0
## [127] statmod_1.5.0 shiny_1.8.0
## [129] highr_0.10 memoise_2.0.1.9000
## [131] bslib_0.6.1 bit_4.0.5
END of report