date generated: 2022-08-22
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
## A4GALT 0.5563104
## AAAS -9.3505565
## AACS 17.4368054
## AAGAB 0.6211840
## AAK1 10.8699941
## AAMDC -5.4631631
Here are some metrics about the input data profile:
| Profile metrics | |
|---|---|
| num_genesets | 2551 |
| num_genes_in_profile | 12290 |
| duplicated_genes_present | 0 |
| num_profile_genes_in_sets | 7289 |
| num_profile_genes_not_in_sets | 5001 |
Here is a plot of the input profiles. Note the dynamic ranges.
Here is the contour plot of the profile including all detected genes.
| Gene sets metrics | |
|---|---|
| num_genesets | 2551 |
| num_genesets_excluded | 1183 |
| num_genesets_included | 1368 |
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.
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| tRNA processing in the mitochondrion | 18 | 2.56e-07 | -0.701 | 8.76e-06 |
| Cholesterol biosynthesis | 26 | 1.02e-09 | 0.692 | 4.97e-08 |
| rRNA processing in the mitochondrion | 21 | 8.74e-07 | -0.620 | 2.54e-05 |
| MET activates PTK2 signaling | 12 | 6.11e-04 | 0.571 | 8.12e-03 |
| ALK mutants bind TKIs | 10 | 2.10e-03 | 0.562 | 2.07e-02 |
| Laminin interactions | 18 | 3.71e-05 | 0.562 | 7.15e-04 |
| Apoptosis induced DNA fragmentation | 10 | 5.04e-03 | 0.512 | 3.56e-02 |
| Membrane binding and targetting of GAG proteins | 14 | 1.20e-03 | -0.500 | 1.43e-02 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 14 | 1.20e-03 | -0.500 | 1.43e-02 |
| Formation of a pool of free 40S subunits | 79 | 4.97e-14 | -0.490 | 1.72e-11 |
| Peptide chain elongation | 67 | 4.04e-12 | -0.490 | 4.60e-10 |
| Syndecan interactions | 19 | 2.68e-04 | 0.483 | 3.95e-03 |
| Eukaryotic Translation Termination | 71 | 3.87e-12 | -0.477 | 4.60e-10 |
| Formation of the ternary complex, and subsequently, the 43S complex | 47 | 1.87e-08 | -0.474 | 7.52e-07 |
| Viral mRNA Translation | 67 | 1.99e-11 | -0.474 | 1.30e-09 |
| Telomere C-strand synthesis initiation | 13 | 3.38e-03 | -0.470 | 2.82e-02 |
| Mitochondrial translation initiation | 88 | 2.75e-14 | -0.470 | 1.72e-11 |
| Mitochondrial translation termination | 88 | 5.02e-14 | -0.465 | 1.72e-11 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 54 | 3.89e-09 | 0.463 | 1.77e-07 |
| Eukaryotic Translation Elongation | 70 | 4.54e-11 | -0.455 | 2.82e-09 |
| Mitochondrial translation elongation | 88 | 1.93e-13 | -0.454 | 4.40e-11 |
| Activation of gene expression by SREBF (SREBP) | 41 | 5.14e-07 | 0.453 | 1.60e-05 |
| Cytosolic tRNA aminoacylation | 24 | 1.28e-04 | 0.452 | 2.06e-03 |
| Selenocysteine synthesis | 71 | 5.83e-11 | -0.450 | 3.32e-09 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | 23 | 2.18e-04 | -0.445 | 3.32e-03 |
| Mitochondrial translation | 94 | 1.17e-13 | -0.443 | 3.20e-11 |
| MET promotes cell motility | 22 | 3.22e-04 | 0.443 | 4.60e-03 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 72 | 9.27e-11 | -0.442 | 4.88e-09 |
| Response of EIF2AK1 (HRI) to heme deficiency | 15 | 3.12e-03 | 0.441 | 2.73e-02 |
| Assembly Of The HIV Virion | 16 | 2.28e-03 | -0.441 | 2.21e-02 |
| Complex I biogenesis | 56 | 1.28e-08 | -0.440 | 5.46e-07 |
| SARS-CoV-2 modulates host translation machinery | 45 | 3.63e-07 | -0.438 | 1.21e-05 |
| Regulation of innate immune responses to cytosolic DNA | 13 | 6.51e-03 | -0.436 | 4.20e-02 |
| Kinesins | 36 | 6.46e-06 | 0.435 | 1.64e-04 |
| PKA activation | 13 | 6.68e-03 | 0.435 | 4.21e-02 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 88 | 6.67e-12 | -0.424 | 5.98e-10 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 90 | 6.99e-12 | -0.419 | 5.98e-10 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 92 | 5.54e-12 | -0.416 | 5.41e-10 |
| Nonsense-Mediated Decay (NMD) | 92 | 5.54e-12 | -0.416 | 5.41e-10 |
| CLEC7A (Dectin-1) induces NFAT activation | 10 | 2.32e-02 | 0.415 | 1.06e-01 |
| Chondroitin sulfate biosynthesis | 16 | 4.88e-03 | 0.407 | 3.51e-02 |
| Non-integrin membrane-ECM interactions | 34 | 4.44e-05 | 0.405 | 8.20e-04 |
| HS-GAG degradation | 18 | 3.04e-03 | 0.404 | 2.68e-02 |
| Formation of ATP by chemiosmotic coupling | 17 | 4.05e-03 | -0.403 | 3.16e-02 |
| Signaling by FLT3 fusion proteins | 19 | 2.42e-03 | 0.402 | 2.29e-02 |
| Nephrin family interactions | 19 | 2.43e-03 | 0.402 | 2.29e-02 |
| Collagen chain trimerization | 26 | 4.18e-04 | 0.400 | 5.78e-03 |
| Elastic fibre formation | 31 | 1.19e-04 | 0.399 | 1.94e-03 |
| Cap-dependent Translation Initiation | 96 | 1.41e-11 | -0.399 | 9.73e-10 |
| Eukaryotic Translation Initiation | 96 | 1.41e-11 | -0.399 | 9.73e-10 |
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| tRNA processing in the mitochondrion | 18 | 2.56e-07 | -7.01e-01 | 8.76e-06 |
| Cholesterol biosynthesis | 26 | 1.02e-09 | 6.92e-01 | 4.97e-08 |
| rRNA processing in the mitochondrion | 21 | 8.74e-07 | -6.20e-01 | 2.54e-05 |
| MET activates PTK2 signaling | 12 | 6.11e-04 | 5.71e-01 | 8.12e-03 |
| ALK mutants bind TKIs | 10 | 2.10e-03 | 5.62e-01 | 2.07e-02 |
| Laminin interactions | 18 | 3.71e-05 | 5.62e-01 | 7.15e-04 |
| Apoptosis induced DNA fragmentation | 10 | 5.04e-03 | 5.12e-01 | 3.56e-02 |
| Membrane binding and targetting of GAG proteins | 14 | 1.20e-03 | -5.00e-01 | 1.43e-02 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 14 | 1.20e-03 | -5.00e-01 | 1.43e-02 |
| Formation of a pool of free 40S subunits | 79 | 4.97e-14 | -4.90e-01 | 1.72e-11 |
| Peptide chain elongation | 67 | 4.04e-12 | -4.90e-01 | 4.60e-10 |
| Syndecan interactions | 19 | 2.68e-04 | 4.83e-01 | 3.95e-03 |
| Eukaryotic Translation Termination | 71 | 3.87e-12 | -4.77e-01 | 4.60e-10 |
| Formation of the ternary complex, and subsequently, the 43S complex | 47 | 1.87e-08 | -4.74e-01 | 7.52e-07 |
| Viral mRNA Translation | 67 | 1.99e-11 | -4.74e-01 | 1.30e-09 |
| Telomere C-strand synthesis initiation | 13 | 3.38e-03 | -4.70e-01 | 2.82e-02 |
| Mitochondrial translation initiation | 88 | 2.75e-14 | -4.70e-01 | 1.72e-11 |
| Mitochondrial translation termination | 88 | 5.02e-14 | -4.65e-01 | 1.72e-11 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 54 | 3.89e-09 | 4.63e-01 | 1.77e-07 |
| Eukaryotic Translation Elongation | 70 | 4.54e-11 | -4.55e-01 | 2.82e-09 |
| Mitochondrial translation elongation | 88 | 1.93e-13 | -4.54e-01 | 4.40e-11 |
| Activation of gene expression by SREBF (SREBP) | 41 | 5.14e-07 | 4.53e-01 | 1.60e-05 |
| Cytosolic tRNA aminoacylation | 24 | 1.28e-04 | 4.52e-01 | 2.06e-03 |
| Selenocysteine synthesis | 71 | 5.83e-11 | -4.50e-01 | 3.32e-09 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | 23 | 2.18e-04 | -4.45e-01 | 3.32e-03 |
| Mitochondrial translation | 94 | 1.17e-13 | -4.43e-01 | 3.20e-11 |
| MET promotes cell motility | 22 | 3.22e-04 | 4.43e-01 | 4.60e-03 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 72 | 9.27e-11 | -4.42e-01 | 4.88e-09 |
| Response of EIF2AK1 (HRI) to heme deficiency | 15 | 3.12e-03 | 4.41e-01 | 2.73e-02 |
| Assembly Of The HIV Virion | 16 | 2.28e-03 | -4.41e-01 | 2.21e-02 |
| Complex I biogenesis | 56 | 1.28e-08 | -4.40e-01 | 5.46e-07 |
| SARS-CoV-2 modulates host translation machinery | 45 | 3.63e-07 | -4.38e-01 | 1.21e-05 |
| Regulation of innate immune responses to cytosolic DNA | 13 | 6.51e-03 | -4.36e-01 | 4.20e-02 |
| Kinesins | 36 | 6.46e-06 | 4.35e-01 | 1.64e-04 |
| PKA activation | 13 | 6.68e-03 | 4.35e-01 | 4.21e-02 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 88 | 6.67e-12 | -4.24e-01 | 5.98e-10 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 90 | 6.99e-12 | -4.19e-01 | 5.98e-10 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 92 | 5.54e-12 | -4.16e-01 | 5.41e-10 |
| Nonsense-Mediated Decay (NMD) | 92 | 5.54e-12 | -4.16e-01 | 5.41e-10 |
| CLEC7A (Dectin-1) induces NFAT activation | 10 | 2.32e-02 | 4.15e-01 | 1.06e-01 |
| Chondroitin sulfate biosynthesis | 16 | 4.88e-03 | 4.07e-01 | 3.51e-02 |
| Non-integrin membrane-ECM interactions | 34 | 4.44e-05 | 4.05e-01 | 8.20e-04 |
| HS-GAG degradation | 18 | 3.04e-03 | 4.04e-01 | 2.68e-02 |
| Formation of ATP by chemiosmotic coupling | 17 | 4.05e-03 | -4.03e-01 | 3.16e-02 |
| Signaling by FLT3 fusion proteins | 19 | 2.42e-03 | 4.02e-01 | 2.29e-02 |
| Nephrin family interactions | 19 | 2.43e-03 | 4.02e-01 | 2.29e-02 |
| Collagen chain trimerization | 26 | 4.18e-04 | 4.00e-01 | 5.78e-03 |
| Elastic fibre formation | 31 | 1.19e-04 | 3.99e-01 | 1.94e-03 |
| Cap-dependent Translation Initiation | 96 | 1.41e-11 | -3.99e-01 | 9.73e-10 |
| Eukaryotic Translation Initiation | 96 | 1.41e-11 | -3.99e-01 | 9.73e-10 |
| Signaling by BMP | 17 | 4.70e-03 | 3.96e-01 | 3.44e-02 |
| Collagen formation | 61 | 1.06e-07 | 3.94e-01 | 3.91e-06 |
| Amino acid transport across the plasma membrane | 23 | 1.28e-03 | 3.88e-01 | 1.48e-02 |
| Synthesis of PIPs at the late endosome membrane | 11 | 2.60e-02 | 3.88e-01 | 1.15e-01 |
| Signaling by PDGFR in disease | 17 | 5.72e-03 | 3.87e-01 | 3.82e-02 |
| LDL clearance | 17 | 5.73e-03 | 3.87e-01 | 3.82e-02 |
| Translation initiation complex formation | 53 | 1.18e-06 | -3.86e-01 | 3.37e-05 |
| Collagen biosynthesis and modifying enzymes | 46 | 6.95e-06 | 3.83e-01 | 1.70e-04 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 54 | 1.35e-06 | -3.80e-01 | 3.77e-05 |
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 123 | 4.24e-13 | -3.79e-01 | 8.29e-11 |
| Tight junction interactions | 12 | 2.39e-02 | -3.77e-01 | 1.08e-01 |
| RAF-independent MAPK1/3 activation | 22 | 2.24e-03 | 3.77e-01 | 2.18e-02 |
| HDMs demethylate histones | 21 | 2.91e-03 | 3.75e-01 | 2.60e-02 |
| Respiratory electron transport | 102 | 6.23e-11 | -3.75e-01 | 3.41e-09 |
| Synthesis of PIPs at the early endosome membrane | 15 | 1.20e-02 | 3.75e-01 | 6.60e-02 |
| Mitotic Telophase/Cytokinesis | 13 | 2.09e-02 | 3.70e-01 | 9.93e-02 |
| Ribosomal scanning and start codon recognition | 54 | 2.73e-06 | -3.69e-01 | 7.32e-05 |
| Chondroitin sulfate/dermatan sulfate metabolism | 43 | 3.02e-05 | 3.68e-01 | 6.42e-04 |
| RHO GTPases Activate NADPH Oxidases | 13 | 2.26e-02 | -3.65e-01 | 1.04e-01 |
| Signaling by FGFR2 IIIa TM | 19 | 5.93e-03 | -3.65e-01 | 3.94e-02 |
| Prolonged ERK activation events | 13 | 2.31e-02 | 3.64e-01 | 1.06e-01 |
| Sensory processing of sound by outer hair cells of the cochlea | 27 | 1.08e-03 | 3.64e-01 | 1.34e-02 |
| Interleukin-6 signaling | 10 | 5.07e-02 | 3.57e-01 | 1.78e-01 |
| Glucagon-type ligand receptors | 12 | 3.27e-02 | -3.56e-01 | 1.36e-01 |
| Prostacyclin signalling through prostacyclin receptor | 12 | 3.27e-02 | -3.56e-01 | 1.36e-01 |
| Formation of the Early Elongation Complex | 33 | 4.12e-04 | -3.55e-01 | 5.75e-03 |
| Formation of the HIV-1 Early Elongation Complex | 33 | 4.12e-04 | -3.55e-01 | 5.75e-03 |
| Molecules associated with elastic fibres | 22 | 3.92e-03 | 3.55e-01 | 3.12e-02 |
| Inhibition of DNA recombination at telomere | 27 | 1.53e-03 | -3.52e-01 | 1.69e-02 |
| Establishment of Sister Chromatid Cohesion | 11 | 4.35e-02 | 3.52e-01 | 1.61e-01 |
| ECM proteoglycans | 33 | 4.84e-04 | 3.51e-01 | 6.56e-03 |
| Regulation of expression of SLITs and ROBOs | 138 | 1.25e-12 | -3.51e-01 | 1.90e-10 |
| Assembly of collagen fibrils and other multimeric structures | 39 | 1.62e-04 | 3.49e-01 | 2.58e-03 |
| PKA-mediated phosphorylation of CREB | 15 | 1.95e-02 | 3.48e-01 | 9.63e-02 |
| PIWI-interacting RNA (piRNA) biogenesis | 16 | 1.59e-02 | -3.48e-01 | 8.27e-02 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 12 | 3.68e-02 | 3.48e-01 | 1.47e-01 |
| Defective EXT2 causes exostoses 2 | 12 | 3.68e-02 | 3.48e-01 | 1.47e-01 |
| Cohesin Loading onto Chromatin | 10 | 5.71e-02 | 3.48e-01 | 1.88e-01 |
| PKA activation in glucagon signalling | 12 | 3.73e-02 | 3.47e-01 | 1.48e-01 |
| Pausing and recovery of Tat-mediated HIV elongation | 30 | 1.08e-03 | -3.45e-01 | 1.34e-02 |
| Tat-mediated HIV elongation arrest and recovery | 30 | 1.08e-03 | -3.45e-01 | 1.34e-02 |
| RNA Pol II CTD phosphorylation and interaction with CE | 27 | 1.94e-03 | -3.45e-01 | 1.97e-02 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 27 | 1.94e-03 | -3.45e-01 | 1.97e-02 |
| RNA Polymerase III Transcription Termination | 21 | 6.43e-03 | -3.44e-01 | 4.19e-02 |
| Budding and maturation of HIV virion | 26 | 2.52e-03 | -3.42e-01 | 2.33e-02 |
| Mucopolysaccharidoses | 11 | 4.96e-02 | 3.42e-01 | 1.76e-01 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 19 | 1.01e-02 | 3.41e-01 | 5.72e-02 |
| Defective B4GALT7 causes EDS, progeroid type | 17 | 1.63e-02 | 3.37e-01 | 8.40e-02 |
| Cristae formation | 30 | 1.43e-03 | -3.37e-01 | 1.60e-02 |
| Receptor Mediated Mitophagy | 10 | 6.77e-02 | -3.34e-01 | 2.14e-01 |
| Acyl chain remodelling of PE | 13 | 3.74e-02 | -3.33e-01 | 1.48e-01 |
| Signaling by ALK fusions and activated point mutants | 52 | 3.26e-05 | 3.33e-01 | 6.47e-04 |
| Signaling by ALK in cancer | 52 | 3.26e-05 | 3.33e-01 | 6.47e-04 |
| FCGR3A-mediated IL10 synthesis | 26 | 3.32e-03 | 3.33e-01 | 2.80e-02 |
| Synthesis of PIPs at the Golgi membrane | 15 | 2.57e-02 | 3.33e-01 | 1.15e-01 |
| p38MAPK events | 12 | 4.63e-02 | -3.32e-01 | 1.68e-01 |
| mRNA Capping | 29 | 2.06e-03 | -3.31e-01 | 2.04e-02 |
| A tetrasaccharide linker sequence is required for GAG synthesis | 22 | 7.49e-03 | 3.29e-01 | 4.57e-02 |
| Repression of WNT target genes | 14 | 3.32e-02 | -3.29e-01 | 1.37e-01 |
| RNA Polymerase I Transcription Termination | 30 | 1.89e-03 | -3.28e-01 | 1.96e-02 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | 17 | 2.04e-02 | 3.25e-01 | 9.76e-02 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 79 | 6.78e-07 | -3.24e-01 | 2.02e-05 |
| SRP-dependent cotranslational protein targeting to membrane | 89 | 1.36e-07 | -3.24e-01 | 4.90e-06 |
| IRAK4 deficiency (TLR2/4) | 10 | 7.66e-02 | -3.23e-01 | 2.34e-01 |
| HIV elongation arrest and recovery | 32 | 1.57e-03 | -3.23e-01 | 1.69e-02 |
| Pausing and recovery of HIV elongation | 32 | 1.57e-03 | -3.23e-01 | 1.69e-02 |
| Zinc transporters | 12 | 5.28e-02 | 3.23e-01 | 1.82e-01 |
| Mitochondrial iron-sulfur cluster biogenesis | 11 | 6.54e-02 | -3.21e-01 | 2.10e-01 |
| Metabolism of folate and pterines | 16 | 2.79e-02 | 3.18e-01 | 1.22e-01 |
| NRAGE signals death through JNK | 45 | 2.67e-04 | 3.14e-01 | 3.95e-03 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | 13 | 5.06e-02 | 3.13e-01 | 1.78e-01 |
| Interaction between L1 and Ankyrins | 12 | 6.15e-02 | 3.12e-01 | 2.01e-01 |
| G beta:gamma signalling through BTK | 11 | 7.74e-02 | -3.08e-01 | 2.35e-01 |
| ATF6 (ATF6-alpha) activates chaperones | 12 | 6.60e-02 | 3.07e-01 | 2.11e-01 |
| PI-3K cascade:FGFR1 | 13 | 5.60e-02 | 3.06e-01 | 1.87e-01 |
| p130Cas linkage to MAPK signaling for integrins | 13 | 5.66e-02 | 3.05e-01 | 1.87e-01 |
| Inwardly rectifying K+ channels | 16 | 3.47e-02 | -3.05e-01 | 1.41e-01 |
| Activation of G protein gated Potassium channels | 15 | 4.15e-02 | -3.04e-01 | 1.57e-01 |
| G protein gated Potassium channels | 15 | 4.15e-02 | -3.04e-01 | 1.57e-01 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 15 | 4.15e-02 | -3.04e-01 | 1.57e-01 |
| Metal ion SLC transporters | 18 | 2.60e-02 | 3.03e-01 | 1.15e-01 |
| Spry regulation of FGF signaling | 16 | 3.66e-02 | -3.02e-01 | 1.47e-01 |
| Selenoamino acid metabolism | 92 | 6.22e-07 | -3.01e-01 | 1.89e-05 |
| Hyaluronan metabolism | 15 | 4.46e-02 | 3.00e-01 | 1.64e-01 |
| Diseases associated with glycosaminoglycan metabolism | 33 | 2.96e-03 | 2.99e-01 | 2.63e-02 |
| SUMOylation of DNA methylation proteins | 16 | 4.12e-02 | -2.95e-01 | 1.57e-01 |
| Signaling by NTRK3 (TRKC) | 15 | 4.89e-02 | 2.94e-01 | 1.75e-01 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 27 | 8.33e-03 | 2.93e-01 | 4.93e-02 |
| Influenza Viral RNA Transcription and Replication | 113 | 7.89e-08 | -2.93e-01 | 3.00e-06 |
| Glycogen storage diseases | 13 | 7.13e-02 | -2.89e-01 | 2.23e-01 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 42 | 1.22e-03 | -2.89e-01 | 1.43e-02 |
| HIV Transcription Elongation | 42 | 1.22e-03 | -2.89e-01 | 1.43e-02 |
| Tat-mediated elongation of the HIV-1 transcript | 42 | 1.22e-03 | -2.89e-01 | 1.43e-02 |
| Plasma lipoprotein assembly | 12 | 8.42e-02 | -2.88e-01 | 2.47e-01 |
| ADP signalling through P2Y purinoceptor 1 | 16 | 4.69e-02 | -2.87e-01 | 1.69e-01 |
| tRNA Aminoacylation | 42 | 1.33e-03 | 2.86e-01 | 1.51e-02 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 11 | 1.03e-01 | 2.84e-01 | 2.80e-01 |
| alpha-linolenic acid (ALA) metabolism | 11 | 1.03e-01 | 2.84e-01 | 2.80e-01 |
| RHOA GTPase cycle | 131 | 2.06e-08 | 2.84e-01 | 8.05e-07 |
| RHOB GTPase cycle | 64 | 9.89e-05 | 2.82e-01 | 1.63e-03 |
| RHOC GTPase cycle | 71 | 4.24e-05 | 2.81e-01 | 7.95e-04 |
| Activation of the AP-1 family of transcription factors | 10 | 1.25e-01 | -2.80e-01 | 3.17e-01 |
| COPI-dependent Golgi-to-ER retrograde traffic | 75 | 2.80e-05 | 2.80e-01 | 6.18e-04 |
| G-protein activation | 12 | 9.38e-02 | -2.79e-01 | 2.64e-01 |
| Autodegradation of Cdh1 by Cdh1:APC/C | 61 | 1.69e-04 | -2.79e-01 | 2.65e-03 |
| FGFR2 mutant receptor activation | 24 | 1.83e-02 | -2.78e-01 | 9.14e-02 |
| rRNA processing | 188 | 5.56e-11 | -2.78e-01 | 3.31e-09 |
| Packaging Of Telomere Ends | 12 | 9.61e-02 | -2.77e-01 | 2.69e-01 |
| Resolution of Sister Chromatid Cohesion | 102 | 1.43e-06 | 2.77e-01 | 3.91e-05 |
| ATF6 (ATF6-alpha) activates chaperone genes | 10 | 1.30e-01 | 2.77e-01 | 3.25e-01 |
| Carnitine metabolism | 11 | 1.13e-01 | -2.76e-01 | 2.98e-01 |
| Regulation of signaling by CBL | 16 | 5.62e-02 | 2.76e-01 | 1.87e-01 |
| Formation of HIV elongation complex in the absence of HIV Tat | 44 | 1.60e-03 | -2.75e-01 | 1.71e-02 |
| Role of LAT2/NTAL/LAB on calcium mobilization | 13 | 8.61e-02 | 2.75e-01 | 2.51e-01 |
| Regulation of PTEN mRNA translation | 11 | 1.18e-01 | 2.73e-01 | 3.06e-01 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | 30 | 1.00e-02 | -2.72e-01 | 5.69e-02 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 19 | 4.05e-02 | -2.72e-01 | 1.57e-01 |
| Degradation of cysteine and homocysteine | 12 | 1.06e-01 | -2.70e-01 | 2.85e-01 |
| G beta:gamma signalling through CDC42 | 14 | 8.18e-02 | -2.69e-01 | 2.43e-01 |
| PI3K Cascade | 29 | 1.27e-02 | 2.67e-01 | 6.93e-02 |
| Keratinization | 22 | 3.01e-02 | -2.67e-01 | 1.28e-01 |
| Defective B3GAT3 causes JDSSDHD | 17 | 5.68e-02 | 2.67e-01 | 1.88e-01 |
| Signaling by PDGFRA extracellular domain mutants | 12 | 1.10e-01 | 2.67e-01 | 2.92e-01 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 12 | 1.10e-01 | 2.67e-01 | 2.92e-01 |
| RND1 GTPase cycle | 37 | 5.08e-03 | 2.66e-01 | 3.56e-02 |
| Extracellular matrix organization | 197 | 1.33e-10 | 2.66e-01 | 6.73e-09 |
| IRS-related events triggered by IGF1R | 35 | 6.53e-03 | 2.66e-01 | 4.20e-02 |
| FRS-mediated FGFR1 signaling | 15 | 7.49e-02 | 2.66e-01 | 2.31e-01 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 22 | 3.12e-02 | -2.65e-01 | 1.32e-01 |
| Sulfur amino acid metabolism | 22 | 3.13e-02 | -2.65e-01 | 1.32e-01 |
| Glycosaminoglycan metabolism | 101 | 4.47e-06 | 2.65e-01 | 1.18e-04 |
| IRS-mediated signalling | 33 | 8.64e-03 | 2.64e-01 | 5.03e-02 |
| FGFR1 mutant receptor activation | 25 | 2.23e-02 | 2.64e-01 | 1.04e-01 |
| Signaling by FLT3 ITD and TKD mutants | 15 | 7.66e-02 | 2.64e-01 | 2.34e-01 |
| Expression and translocation of olfactory receptors | 86 | 2.58e-05 | -2.63e-01 | 5.80e-04 |
| Late endosomal microautophagy | 29 | 1.44e-02 | -2.63e-01 | 7.54e-02 |
| APC/C:Cdc20 mediated degradation of Securin | 64 | 2.88e-04 | -2.62e-01 | 4.19e-03 |
| Negative epigenetic regulation of rRNA expression | 56 | 6.92e-04 | -2.62e-01 | 9.02e-03 |
| Signaling by WNT in cancer | 30 | 1.32e-02 | 2.62e-01 | 7.10e-02 |
| TICAM1,TRAF6-dependent induction of TAK1 complex | 11 | 1.34e-01 | -2.61e-01 | 3.28e-01 |
| Gastrulation | 10 | 1.54e-01 | 2.61e-01 | 3.57e-01 |
| Germ layer formation at gastrulation | 10 | 1.54e-01 | 2.61e-01 | 3.57e-01 |
| RHOD GTPase cycle | 50 | 1.44e-03 | 2.61e-01 | 1.61e-02 |
| Frs2-mediated activation | 11 | 1.35e-01 | 2.61e-01 | 3.28e-01 |
| RNA Polymerase III Abortive And Retractive Initiation | 39 | 4.89e-03 | -2.61e-01 | 3.51e-02 |
| RNA Polymerase III Transcription | 39 | 4.89e-03 | -2.61e-01 | 3.51e-02 |
| Signaling by ROBO receptors | 179 | 2.03e-09 | -2.60e-01 | 9.60e-08 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 19 | 4.95e-02 | -2.60e-01 | 1.76e-01 |
| The citric acid (TCA) cycle and respiratory electron transport | 170 | 5.30e-09 | -2.60e-01 | 2.34e-07 |
| NoRC negatively regulates rRNA expression | 53 | 1.15e-03 | -2.58e-01 | 1.41e-02 |
| Synthesis of PIPs at the plasma membrane | 46 | 2.45e-03 | 2.58e-01 | 2.30e-02 |
| IGF1R signaling cascade | 36 | 7.41e-03 | 2.58e-01 | 4.57e-02 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 36 | 7.41e-03 | 2.58e-01 | 4.57e-02 |
| Chaperone Mediated Autophagy | 17 | 6.61e-02 | -2.58e-01 | 2.11e-01 |
| Vif-mediated degradation of APOBEC3G | 50 | 1.67e-03 | -2.57e-01 | 1.77e-02 |
| ADP signalling through P2Y purinoceptor 12 | 14 | 9.71e-02 | -2.56e-01 | 2.70e-01 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 89 | 3.10e-05 | 2.56e-01 | 6.42e-04 |
| Amplification of signal from the kinetochores | 89 | 3.10e-05 | 2.56e-01 | 6.42e-04 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | 15 | 8.70e-02 | -2.55e-01 | 2.52e-01 |
| Regulation of RUNX1 Expression and Activity | 17 | 6.90e-02 | 2.55e-01 | 2.17e-01 |
| ABC transporters in lipid homeostasis | 10 | 1.64e-01 | 2.54e-01 | 3.68e-01 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 14 | 1.00e-01 | -2.54e-01 | 2.77e-01 |
| WNT ligand biogenesis and trafficking | 16 | 7.95e-02 | -2.53e-01 | 2.40e-01 |
| Postmitotic nuclear pore complex (NPC) reformation | 27 | 2.28e-02 | 2.53e-01 | 1.05e-01 |
| NF-kB is activated and signals survival | 12 | 1.29e-01 | -2.53e-01 | 3.25e-01 |
| Negative regulation of NOTCH4 signaling | 51 | 1.85e-03 | -2.52e-01 | 1.93e-02 |
| Formation of the cornified envelope | 18 | 6.41e-02 | -2.52e-01 | 2.06e-01 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 50 | 2.06e-03 | -2.52e-01 | 2.04e-02 |
| Integrin signaling | 22 | 4.29e-02 | 2.49e-01 | 1.59e-01 |
| Fatty acyl-CoA biosynthesis | 29 | 2.01e-02 | 2.49e-01 | 9.70e-02 |
| Vpu mediated degradation of CD4 | 48 | 2.85e-03 | -2.49e-01 | 2.59e-02 |
| Assembly and cell surface presentation of NMDA receptors | 16 | 8.50e-02 | 2.49e-01 | 2.49e-01 |
| IKK complex recruitment mediated by RIP1 | 21 | 4.88e-02 | -2.48e-01 | 1.75e-01 |
| Metabolism of steroids | 111 | 6.69e-06 | 2.48e-01 | 1.66e-04 |
| Heparan sulfate/heparin (HS-GAG) metabolism | 45 | 4.18e-03 | 2.47e-01 | 3.20e-02 |
| Synthesis of PE | 11 | 1.57e-01 | 2.47e-01 | 3.60e-01 |
| RNA Polymerase I Transcription Initiation | 47 | 3.62e-03 | -2.46e-01 | 2.94e-02 |
| PERK regulates gene expression | 29 | 2.25e-02 | 2.45e-01 | 1.04e-01 |
| Polo-like kinase mediated events | 16 | 9.01e-02 | 2.45e-01 | 2.57e-01 |
| Synthesis of very long-chain fatty acyl-CoAs | 18 | 7.27e-02 | 2.44e-01 | 2.26e-01 |
| G alpha (12/13) signalling events | 57 | 1.43e-03 | 2.44e-01 | 1.60e-02 |
| SLBP independent Processing of Histone Pre-mRNAs | 10 | 1.82e-01 | -2.44e-01 | 3.89e-01 |
| Signaling by FGFR1 in disease | 32 | 1.72e-02 | 2.43e-01 | 8.81e-02 |
| Cell surface interactions at the vascular wall | 94 | 4.64e-05 | 2.43e-01 | 8.36e-04 |
| FLT3 signaling in disease | 27 | 2.90e-02 | 2.43e-01 | 1.25e-01 |
| Autodegradation of the E3 ubiquitin ligase COP1 | 48 | 3.63e-03 | -2.43e-01 | 2.94e-02 |
| EML4 and NUDC in mitotic spindle formation | 93 | 5.31e-05 | 2.43e-01 | 9.32e-04 |
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 49 | 3.31e-03 | -2.43e-01 | 2.80e-02 |
| p53-Independent DNA Damage Response | 49 | 3.31e-03 | -2.43e-01 | 2.80e-02 |
| p53-Independent G1/S DNA damage checkpoint | 49 | 3.31e-03 | -2.43e-01 | 2.80e-02 |
| Synthesis of IP2, IP, and Ins in the cytosol | 12 | 1.46e-01 | 2.42e-01 | 3.46e-01 |
| Signaling by cytosolic FGFR1 fusion mutants | 18 | 7.64e-02 | 2.41e-01 | 2.34e-01 |
| ATF4 activates genes in response to endoplasmic reticulum stress | 24 | 4.09e-02 | 2.41e-01 | 1.57e-01 |
| Translation | 267 | 1.42e-11 | -2.41e-01 | 9.73e-10 |
| FCERI mediated Ca+2 mobilization | 21 | 5.65e-02 | 2.40e-01 | 1.87e-01 |
| Plasma lipoprotein clearance | 30 | 2.28e-02 | 2.40e-01 | 1.05e-01 |
| Early SARS-CoV-2 Infection Events | 29 | 2.54e-02 | 2.40e-01 | 1.14e-01 |
| Recycling pathway of L1 | 24 | 4.23e-02 | 2.40e-01 | 1.59e-01 |
| Degradation of DVL | 53 | 2.61e-03 | -2.39e-01 | 2.40e-02 |
| Retinoid metabolism and transport | 24 | 4.28e-02 | 2.39e-01 | 1.59e-01 |
| Olfactory Signaling Pathway | 90 | 9.57e-05 | -2.38e-01 | 1.60e-03 |
| Inactivation of CSF3 (G-CSF) signaling | 21 | 5.92e-02 | -2.38e-01 | 1.94e-01 |
| Oncogenic MAPK signaling | 73 | 4.59e-04 | 2.37e-01 | 6.28e-03 |
| Depolymerisation of the Nuclear Lamina | 14 | 1.25e-01 | 2.37e-01 | 3.17e-01 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 47 | 5.15e-03 | -2.36e-01 | 3.59e-02 |
| Integrin cell surface interactions | 44 | 6.80e-03 | 2.36e-01 | 4.27e-02 |
| Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 10 | 1.97e-01 | 2.35e-01 | 4.12e-01 |
| Apoptotic execution phase | 42 | 8.37e-03 | 2.35e-01 | 4.93e-02 |
| SCF-beta-TrCP mediated degradation of Emi1 | 52 | 3.37e-03 | -2.35e-01 | 2.82e-02 |
| APC-Cdc20 mediated degradation of Nek2A | 25 | 4.22e-02 | -2.35e-01 | 1.59e-01 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 21 | 6.26e-02 | 2.35e-01 | 2.04e-01 |
| Major pathway of rRNA processing in the nucleolus and cytosol | 157 | 4.62e-07 | -2.34e-01 | 1.51e-05 |
| NCAM signaling for neurite out-growth | 41 | 9.73e-03 | 2.33e-01 | 5.55e-02 |
| rRNA processing in the nucleus and cytosol | 167 | 2.08e-07 | -2.33e-01 | 7.29e-06 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 15 | 1.18e-01 | 2.33e-01 | 3.06e-01 |
| Collagen degradation | 20 | 7.12e-02 | 2.33e-01 | 2.23e-01 |
| SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 11 | 1.82e-01 | -2.33e-01 | 3.89e-01 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 70 | 7.97e-04 | -2.32e-01 | 1.02e-02 |
| mRNA Splicing - Minor Pathway | 50 | 4.57e-03 | -2.32e-01 | 3.39e-02 |
| Polymerase switching on the C-strand of the telomere | 25 | 4.49e-02 | -2.32e-01 | 1.64e-01 |
| Glutathione synthesis and recycling | 10 | 2.05e-01 | 2.32e-01 | 4.17e-01 |
| VEGFR2 mediated cell proliferation | 16 | 1.09e-01 | 2.32e-01 | 2.90e-01 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 51 | 4.50e-03 | -2.30e-01 | 3.38e-02 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 23 | 5.62e-02 | -2.30e-01 | 1.87e-01 |
| Unwinding of DNA | 12 | 1.68e-01 | 2.30e-01 | 3.72e-01 |
| TRAF3-dependent IRF activation pathway | 12 | 1.69e-01 | 2.29e-01 | 3.72e-01 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | 57 | 2.86e-03 | -2.29e-01 | 2.59e-02 |
| Signaling by BRAF and RAF1 fusions | 57 | 2.88e-03 | 2.28e-01 | 2.59e-02 |
| RNA Polymerase III Chain Elongation | 16 | 1.14e-01 | -2.28e-01 | 2.98e-01 |
| ERKs are inactivated | 12 | 1.71e-01 | -2.28e-01 | 3.76e-01 |
| Influenza Infection | 130 | 7.59e-06 | -2.28e-01 | 1.82e-04 |
| Degradation of GLI1 by the proteasome | 55 | 3.80e-03 | -2.26e-01 | 3.06e-02 |
| Export of Viral Ribonucleoproteins from Nucleus | 32 | 2.72e-02 | 2.26e-01 | 1.19e-01 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 52 | 4.92e-03 | -2.26e-01 | 3.51e-02 |
| RHO GTPases Activate Formins | 115 | 3.14e-05 | 2.25e-01 | 6.42e-04 |
| CTNNB1 S33 mutants aren’t phosphorylated | 15 | 1.32e-01 | 2.25e-01 | 3.25e-01 |
| CTNNB1 S37 mutants aren’t phosphorylated | 15 | 1.32e-01 | 2.25e-01 | 3.25e-01 |
| CTNNB1 S45 mutants aren’t phosphorylated | 15 | 1.32e-01 | 2.25e-01 | 3.25e-01 |
| CTNNB1 T41 mutants aren’t phosphorylated | 15 | 1.32e-01 | 2.25e-01 | 3.25e-01 |
| Signaling by CTNNB1 phospho-site mutants | 15 | 1.32e-01 | 2.25e-01 | 3.25e-01 |
| Signaling by GSK3beta mutants | 15 | 1.32e-01 | 2.25e-01 | 3.25e-01 |
| Transport of bile salts and organic acids, metal ions and amine compounds | 46 | 8.48e-03 | 2.24e-01 | 4.96e-02 |
| Regulation of Apoptosis | 50 | 6.25e-03 | -2.24e-01 | 4.09e-02 |
| Downstream signaling of activated FGFR1 | 23 | 6.36e-02 | 2.24e-01 | 2.06e-01 |
| PI-3K cascade:FGFR3 | 11 | 2.01e-01 | 2.23e-01 | 4.15e-01 |
| PI-3K cascade:FGFR4 | 11 | 2.01e-01 | 2.23e-01 | 4.15e-01 |
| Insulin receptor signalling cascade | 38 | 1.81e-02 | 2.22e-01 | 9.06e-02 |
| Effects of PIP2 hydrolysis | 18 | 1.04e-01 | 2.22e-01 | 2.82e-01 |
| Mitochondrial protein import | 56 | 4.17e-03 | -2.22e-01 | 3.20e-02 |
| RHO GTPases activate CIT | 17 | 1.14e-01 | 2.21e-01 | 2.98e-01 |
| SIRT1 negatively regulates rRNA expression | 15 | 1.38e-01 | -2.21e-01 | 3.34e-01 |
| Ubiquitin-dependent degradation of Cyclin D | 49 | 7.47e-03 | -2.21e-01 | 4.57e-02 |
| RNA Polymerase I Promoter Escape | 38 | 1.89e-02 | -2.20e-01 | 9.35e-02 |
| RNA Polymerase I Promoter Clearance | 57 | 4.08e-03 | -2.20e-01 | 3.16e-02 |
| RNA Polymerase I Transcription | 57 | 4.08e-03 | -2.20e-01 | 3.16e-02 |
| Gamma carboxylation, hypusine formation and arylsulfatase activation | 29 | 4.13e-02 | 2.19e-01 | 1.57e-01 |
| Dectin-1 mediated noncanonical NF-kB signaling | 57 | 4.27e-03 | -2.19e-01 | 3.25e-02 |
| CDK-mediated phosphorylation and removal of Cdc6 | 68 | 1.82e-03 | -2.19e-01 | 1.91e-02 |
| Mitochondrial Fatty Acid Beta-Oxidation | 32 | 3.23e-02 | -2.19e-01 | 1.35e-01 |
| NRIF signals cell death from the nucleus | 15 | 1.43e-01 | -2.19e-01 | 3.42e-01 |
| RHOG GTPase cycle | 65 | 2.33e-03 | 2.19e-01 | 2.23e-02 |
| DAG and IP3 signaling | 32 | 3.27e-02 | 2.18e-01 | 1.36e-01 |
| Hh mutants are degraded by ERAD | 52 | 6.52e-03 | -2.18e-01 | 4.20e-02 |
| SCF(Skp2)-mediated degradation of p27/p21 | 57 | 4.44e-03 | -2.18e-01 | 3.36e-02 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 61 | 3.30e-03 | -2.18e-01 | 2.80e-02 |
| Stabilization of p53 | 52 | 6.68e-03 | -2.18e-01 | 4.21e-02 |
| p53-Dependent G1 DNA Damage Response | 60 | 3.59e-03 | -2.18e-01 | 2.94e-02 |
| p53-Dependent G1/S DNA damage checkpoint | 60 | 3.59e-03 | -2.18e-01 | 2.94e-02 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 10 | 2.35e-01 | 2.17e-01 | 4.58e-01 |
| Protein methylation | 15 | 1.46e-01 | -2.17e-01 | 3.46e-01 |
| Cytoprotection by HMOX1 | 57 | 4.84e-03 | -2.16e-01 | 3.51e-02 |
| Mitophagy | 25 | 6.39e-02 | -2.14e-01 | 2.06e-01 |
| FGFR2 alternative splicing | 25 | 6.48e-02 | -2.13e-01 | 2.08e-01 |
| IRAK2 mediated activation of TAK1 complex | 10 | 2.43e-01 | -2.13e-01 | 4.67e-01 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 21 | 9.15e-02 | 2.13e-01 | 2.60e-01 |
| Interferon gamma signaling | 51 | 8.69e-03 | -2.13e-01 | 5.04e-02 |
| Negative regulation of FLT3 | 12 | 2.02e-01 | -2.13e-01 | 4.15e-01 |
| PI Metabolism | 71 | 2.00e-03 | 2.12e-01 | 2.01e-02 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 68 | 2.50e-03 | -2.12e-01 | 2.32e-02 |
| CS/DS degradation | 13 | 1.86e-01 | 2.12e-01 | 3.96e-01 |
| Nuclear Pore Complex (NPC) Disassembly | 35 | 3.12e-02 | 2.11e-01 | 1.32e-01 |
| Triglyceride metabolism | 21 | 9.51e-02 | 2.10e-01 | 2.67e-01 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 14 | 1.73e-01 | -2.10e-01 | 3.78e-01 |
| Golgi-to-ER retrograde transport | 105 | 2.01e-04 | 2.10e-01 | 3.13e-03 |
| Formation of TC-NER Pre-Incision Complex | 53 | 8.30e-03 | -2.10e-01 | 4.93e-02 |
| NIK–>noncanonical NF-kB signaling | 56 | 6.67e-03 | -2.10e-01 | 4.21e-02 |
| PLC beta mediated events | 36 | 2.99e-02 | 2.09e-01 | 1.28e-01 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | 20 | 1.08e-01 | -2.08e-01 | 2.88e-01 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 20 | 1.08e-01 | -2.08e-01 | 2.88e-01 |
| Factors involved in megakaryocyte development and platelet production | 102 | 2.97e-04 | 2.08e-01 | 4.28e-03 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 19 | 1.18e-01 | -2.07e-01 | 3.06e-01 |
| Degradation of GLI2 by the proteasome | 55 | 7.97e-03 | -2.07e-01 | 4.76e-02 |
| CDC42 GTPase cycle | 131 | 4.55e-05 | 2.07e-01 | 8.30e-04 |
| Regulation of IFNG signaling | 12 | 2.16e-01 | -2.06e-01 | 4.34e-01 |
| Dermatan sulfate biosynthesis | 10 | 2.59e-01 | 2.06e-01 | 4.84e-01 |
| Transport of Ribonucleoproteins into the Host Nucleus | 31 | 4.75e-02 | 2.06e-01 | 1.70e-01 |
| Basigin interactions | 20 | 1.13e-01 | 2.05e-01 | 2.98e-01 |
| Formation of RNA Pol II elongation complex | 57 | 7.93e-03 | -2.04e-01 | 4.76e-02 |
| RNA Polymerase II Transcription Elongation | 57 | 7.93e-03 | -2.04e-01 | 4.76e-02 |
| Nucleotide biosynthesis | 12 | 2.23e-01 | 2.03e-01 | 4.39e-01 |
| G1/S DNA Damage Checkpoints | 62 | 5.67e-03 | -2.03e-01 | 3.82e-02 |
| Cleavage of the damaged purine | 16 | 1.59e-01 | -2.03e-01 | 3.61e-01 |
| Depurination | 16 | 1.59e-01 | -2.03e-01 | 3.61e-01 |
| Recognition and association of DNA glycosylase with site containing an affected purine | 16 | 1.59e-01 | -2.03e-01 | 3.61e-01 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 38 | 3.03e-02 | -2.03e-01 | 1.29e-01 |
| NEP/NS2 Interacts with the Cellular Export Machinery | 31 | 5.20e-02 | 2.02e-01 | 1.81e-01 |
| Formation of tubulin folding intermediates by CCT/TriC | 18 | 1.39e-01 | 2.02e-01 | 3.36e-01 |
| IRF3-mediated induction of type I IFN | 11 | 2.47e-01 | -2.02e-01 | 4.72e-01 |
| Beta-catenin phosphorylation cascade | 17 | 1.52e-01 | 2.01e-01 | 3.56e-01 |
| Sensory processing of sound | 41 | 2.66e-02 | 2.00e-01 | 1.17e-01 |
| Hh mutants abrogate ligand secretion | 53 | 1.18e-02 | -2.00e-01 | 6.56e-02 |
| Role of phospholipids in phagocytosis | 19 | 1.32e-01 | 2.00e-01 | 3.25e-01 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 36 | 3.91e-02 | -1.99e-01 | 1.53e-01 |
| MET activates RAP1 and RAC1 | 10 | 2.77e-01 | 1.99e-01 | 5.01e-01 |
| HIV Transcription Initiation | 46 | 2.01e-02 | -1.98e-01 | 9.70e-02 |
| RNA Polymerase II HIV Promoter Escape | 46 | 2.01e-02 | -1.98e-01 | 9.70e-02 |
| RNA Polymerase II Promoter Escape | 46 | 2.01e-02 | -1.98e-01 | 9.70e-02 |
| RNA Polymerase II Transcription Initiation | 46 | 2.01e-02 | -1.98e-01 | 9.70e-02 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 46 | 2.01e-02 | -1.98e-01 | 9.70e-02 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 46 | 2.01e-02 | -1.98e-01 | 9.70e-02 |
| TICAM1, RIP1-mediated IKK complex recruitment | 18 | 1.46e-01 | -1.98e-01 | 3.46e-01 |
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 22 | 1.08e-01 | 1.98e-01 | 2.89e-01 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 69 | 4.60e-03 | -1.97e-01 | 3.39e-02 |
| Regulation of TP53 Activity through Association with Co-factors | 10 | 2.81e-01 | -1.97e-01 | 5.06e-01 |
| RHOV GTPase cycle | 35 | 4.41e-02 | 1.97e-01 | 1.63e-01 |
| Intrinsic Pathway of Fibrin Clot Formation | 11 | 2.59e-01 | -1.97e-01 | 4.84e-01 |
| PI-3K cascade:FGFR2 | 14 | 2.04e-01 | 1.96e-01 | 4.17e-01 |
| NCAM1 interactions | 23 | 1.05e-01 | 1.96e-01 | 2.83e-01 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 76 | 3.26e-03 | 1.95e-01 | 2.80e-02 |
| Nitric oxide stimulates guanylate cyclase | 10 | 2.86e-01 | 1.95e-01 | 5.11e-01 |
| Platelet Aggregation (Plug Formation) | 27 | 8.07e-02 | 1.94e-01 | 2.40e-01 |
| HS-GAG biosynthesis | 25 | 9.29e-02 | 1.94e-01 | 2.63e-01 |
| Rev-mediated nuclear export of HIV RNA | 34 | 5.02e-02 | 1.94e-01 | 1.78e-01 |
| DNA Damage Recognition in GG-NER | 38 | 3.85e-02 | -1.94e-01 | 1.52e-01 |
| Signaling by PDGF | 44 | 2.60e-02 | 1.94e-01 | 1.15e-01 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 26 | 8.70e-02 | -1.94e-01 | 2.52e-01 |
| RNA Polymerase III Transcription Initiation | 34 | 5.05e-02 | -1.94e-01 | 1.78e-01 |
| NS1 Mediated Effects on Host Pathways | 38 | 3.91e-02 | 1.93e-01 | 1.53e-01 |
| Cross-presentation of soluble exogenous antigens (endosomes) | 43 | 2.83e-02 | -1.93e-01 | 1.23e-01 |
| Azathioprine ADME | 18 | 1.56e-01 | 1.93e-01 | 3.60e-01 |
| Signaling by Hippo | 20 | 1.35e-01 | 1.93e-01 | 3.28e-01 |
| GLI3 is processed to GLI3R by the proteasome | 56 | 1.25e-02 | -1.93e-01 | 6.83e-02 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 26 | 8.84e-02 | -1.93e-01 | 2.56e-01 |
| Removal of the Flap Intermediate from the C-strand | 16 | 1.81e-01 | -1.93e-01 | 3.89e-01 |
| Transcription of the HIV genome | 68 | 5.97e-03 | -1.93e-01 | 3.95e-02 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | 71 | 4.98e-03 | -1.93e-01 | 3.53e-02 |
| SUMOylation of DNA replication proteins | 44 | 2.71e-02 | 1.93e-01 | 1.19e-01 |
| RHOF GTPase cycle | 39 | 3.76e-02 | 1.92e-01 | 1.49e-01 |
| RND2 GTPase cycle | 38 | 4.03e-02 | 1.92e-01 | 1.57e-01 |
| Synthesis of PA | 26 | 8.99e-02 | -1.92e-01 | 2.57e-01 |
| FCERI mediated NF-kB activation | 71 | 5.20e-03 | -1.92e-01 | 3.59e-02 |
| Regulation of RUNX2 expression and activity | 66 | 7.19e-03 | -1.92e-01 | 4.47e-02 |
| Cellular response to starvation | 127 | 2.06e-04 | -1.91e-01 | 3.17e-03 |
| DNA methylation | 11 | 2.73e-01 | 1.91e-01 | 4.98e-01 |
| L1CAM interactions | 74 | 4.61e-03 | 1.91e-01 | 3.39e-02 |
| Glyoxylate metabolism and glycine degradation | 23 | 1.14e-01 | -1.91e-01 | 2.98e-01 |
| RNA Polymerase I Promoter Opening | 10 | 2.97e-01 | -1.91e-01 | 5.23e-01 |
| Unfolded Protein Response (UPR) | 86 | 2.32e-03 | 1.90e-01 | 2.23e-02 |
| Other semaphorin interactions | 15 | 2.03e-01 | 1.90e-01 | 4.15e-01 |
| mRNA Splicing | 184 | 9.84e-06 | -1.90e-01 | 2.28e-04 |
| Signaling by MET | 56 | 1.44e-02 | 1.89e-01 | 7.54e-02 |
| FRS-mediated FGFR3 signaling | 13 | 2.39e-01 | 1.89e-01 | 4.61e-01 |
| FRS-mediated FGFR4 signaling | 13 | 2.39e-01 | 1.89e-01 | 4.61e-01 |
| NR1H2 and NR1H3-mediated signaling | 35 | 5.38e-02 | 1.88e-01 | 1.83e-01 |
| Signaling by FGFR4 in disease | 10 | 3.02e-01 | 1.88e-01 | 5.29e-01 |
| Retrograde neurotrophin signalling | 11 | 2.81e-01 | 1.88e-01 | 5.06e-01 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 10 | 3.04e-01 | 1.88e-01 | 5.29e-01 |
| RAC1 GTPase cycle | 154 | 6.23e-05 | 1.87e-01 | 1.08e-03 |
| Metabolism of RNA | 636 | 1.46e-15 | -1.87e-01 | 1.99e-12 |
| Tie2 Signaling | 16 | 1.95e-01 | 1.87e-01 | 4.10e-01 |
| Signalling to RAS | 16 | 1.96e-01 | -1.87e-01 | 4.11e-01 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 11 | 2.85e-01 | -1.86e-01 | 5.11e-01 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 31 | 7.33e-02 | 1.86e-01 | 2.28e-01 |
| Sensory processing of sound by inner hair cells of the cochlea | 39 | 4.48e-02 | 1.86e-01 | 1.64e-01 |
| p75NTR signals via NF-kB | 15 | 2.13e-01 | -1.86e-01 | 4.31e-01 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 29 | 8.38e-02 | 1.86e-01 | 2.47e-01 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 29 | 8.38e-02 | 1.86e-01 | 2.47e-01 |
| Nuclear Envelope Breakdown | 50 | 2.36e-02 | 1.85e-01 | 1.07e-01 |
| Senescence-Associated Secretory Phenotype (SASP) | 52 | 2.11e-02 | -1.85e-01 | 9.97e-02 |
| Signal amplification | 21 | 1.43e-01 | -1.85e-01 | 3.43e-01 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 72 | 6.97e-03 | -1.84e-01 | 4.35e-02 |
| Interactions of Rev with host cellular proteins | 36 | 5.62e-02 | 1.84e-01 | 1.87e-01 |
| Post-translational protein phosphorylation | 70 | 7.90e-03 | 1.84e-01 | 4.76e-02 |
| Pregnenolone biosynthesis | 10 | 3.14e-01 | 1.84e-01 | 5.36e-01 |
| Transport of inorganic cations/anions and amino acids/oligopeptides | 67 | 9.42e-03 | 1.84e-01 | 5.42e-02 |
| Downstream signal transduction | 28 | 9.28e-02 | 1.84e-01 | 2.63e-01 |
| Glycolysis | 64 | 1.12e-02 | 1.84e-01 | 6.23e-02 |
| Sphingolipid de novo biosynthesis | 37 | 5.38e-02 | 1.83e-01 | 1.83e-01 |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 15 | 2.21e-01 | 1.83e-01 | 4.39e-01 |
| Regulation of APC/C activators between G1/S and early anaphase | 76 | 6.08e-03 | -1.82e-01 | 4.00e-02 |
| O-linked glycosylation of mucins | 34 | 6.64e-02 | 1.82e-01 | 2.11e-01 |
| Activation of NF-kappaB in B cells | 62 | 1.33e-02 | -1.82e-01 | 7.12e-02 |
| Acyl chain remodelling of PC | 14 | 2.39e-01 | -1.82e-01 | 4.61e-01 |
| mRNA Splicing - Major Pathway | 176 | 3.34e-05 | -1.82e-01 | 6.53e-04 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 30 | 8.54e-02 | -1.82e-01 | 2.50e-01 |
| SHC-mediated cascade:FGFR1 | 13 | 2.58e-01 | 1.81e-01 | 4.84e-01 |
| Metabolism of fat-soluble vitamins | 27 | 1.04e-01 | 1.81e-01 | 2.82e-01 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 13 | 2.59e-01 | 1.81e-01 | 4.84e-01 |
| Condensation of Prophase Chromosomes | 19 | 1.73e-01 | 1.81e-01 | 3.78e-01 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | 86 | 3.83e-03 | 1.81e-01 | 3.06e-02 |
| GPVI-mediated activation cascade | 22 | 1.44e-01 | 1.80e-01 | 3.44e-01 |
| Formation of Incision Complex in GG-NER | 42 | 4.46e-02 | -1.79e-01 | 1.64e-01 |
| Growth hormone receptor signaling | 20 | 1.65e-01 | -1.79e-01 | 3.68e-01 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 27 | 1.07e-01 | 1.79e-01 | 2.88e-01 |
| TICAM1-dependent activation of IRF3/IRF7 | 12 | 2.83e-01 | -1.79e-01 | 5.08e-01 |
| Degradation of beta-catenin by the destruction complex | 82 | 5.18e-03 | -1.79e-01 | 3.59e-02 |
| Cyclin A:Cdk2-associated events at S phase entry | 82 | 5.29e-03 | -1.78e-01 | 3.62e-02 |
| Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon | 16 | 2.17e-01 | -1.78e-01 | 4.34e-01 |
| TRAF6 mediated IRF7 activation | 14 | 2.49e-01 | 1.78e-01 | 4.74e-01 |
| p75NTR recruits signalling complexes | 12 | 2.87e-01 | -1.77e-01 | 5.13e-01 |
| G-protein mediated events | 40 | 5.22e-02 | 1.77e-01 | 1.81e-01 |
| Defective HDR through Homologous Recombination (HRR) due to BRCA1 loss-of-function | 25 | 1.25e-01 | 1.77e-01 | 3.17e-01 |
| Defective HDR through Homologous Recombination (HRR) due to PALB2 loss of function | 25 | 1.25e-01 | 1.77e-01 | 3.17e-01 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | 25 | 1.25e-01 | 1.77e-01 | 3.17e-01 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | 25 | 1.25e-01 | 1.77e-01 | 3.17e-01 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | 167 | 8.29e-05 | 1.77e-01 | 1.42e-03 |
| SLC transporter disorders | 66 | 1.31e-02 | 1.77e-01 | 7.07e-02 |
| MAPK6/MAPK4 signaling | 84 | 5.22e-03 | -1.77e-01 | 3.59e-02 |
| Nuclear import of Rev protein | 33 | 8.01e-02 | 1.76e-01 | 2.40e-01 |
| Mitotic Prometaphase | 183 | 4.24e-05 | 1.76e-01 | 7.95e-04 |
| Cyclin E associated events during G1/S transition | 80 | 6.61e-03 | -1.76e-01 | 4.21e-02 |
| mRNA decay by 5’ to 3’ exoribonuclease | 15 | 2.40e-01 | -1.75e-01 | 4.62e-01 |
| Mitotic Spindle Checkpoint | 105 | 1.94e-03 | 1.75e-01 | 1.97e-02 |
| Defects in cobalamin (B12) metabolism | 12 | 2.93e-01 | 1.75e-01 | 5.19e-01 |
| Inactivation, recovery and regulation of the phototransduction cascade | 21 | 1.65e-01 | -1.75e-01 | 3.68e-01 |
| The phototransduction cascade | 21 | 1.65e-01 | -1.75e-01 | 3.68e-01 |
| CD28 dependent PI3K/Akt signaling | 19 | 1.87e-01 | 1.75e-01 | 3.96e-01 |
| Signaling by Rho GTPases, Miro GTPases and RHOBTB3 | 565 | 2.45e-12 | 1.74e-01 | 3.35e-10 |
| Thromboxane signalling through TP receptor | 14 | 2.60e-01 | -1.74e-01 | 4.86e-01 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | 33 | 8.42e-02 | 1.74e-01 | 2.47e-01 |
| APC truncation mutants have impaired AXIN binding | 14 | 2.65e-01 | 1.72e-01 | 4.88e-01 |
| AXIN missense mutants destabilize the destruction complex | 14 | 2.65e-01 | 1.72e-01 | 4.88e-01 |
| Signaling by AMER1 mutants | 14 | 2.65e-01 | 1.72e-01 | 4.88e-01 |
| Signaling by APC mutants | 14 | 2.65e-01 | 1.72e-01 | 4.88e-01 |
| Signaling by AXIN mutants | 14 | 2.65e-01 | 1.72e-01 | 4.88e-01 |
| Truncations of AMER1 destabilize the destruction complex | 14 | 2.65e-01 | 1.72e-01 | 4.88e-01 |
| FRS-mediated FGFR2 signaling | 16 | 2.34e-01 | 1.72e-01 | 4.57e-01 |
| Defects in vitamin and cofactor metabolism | 20 | 1.83e-01 | 1.72e-01 | 3.91e-01 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 15 | 2.50e-01 | -1.72e-01 | 4.74e-01 |
| Signaling by Rho GTPases | 551 | 1.01e-11 | 1.71e-01 | 8.13e-10 |
| Signaling by NOTCH4 | 77 | 9.56e-03 | -1.71e-01 | 5.47e-02 |
| Interactions of Vpr with host cellular proteins | 33 | 9.01e-02 | 1.71e-01 | 2.57e-01 |
| Regulation of RUNX3 expression and activity | 52 | 3.47e-02 | -1.69e-01 | 1.41e-01 |
| RHO GTPase cycle | 386 | 1.45e-08 | 1.69e-01 | 5.99e-07 |
| Translesion synthesis by POLI | 17 | 2.28e-01 | -1.69e-01 | 4.48e-01 |
| Activation of HOX genes during differentiation | 66 | 1.80e-02 | -1.69e-01 | 9.03e-02 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 66 | 1.80e-02 | -1.69e-01 | 9.03e-02 |
| Signaling by Erythropoietin | 22 | 1.72e-01 | 1.68e-01 | 3.76e-01 |
| Downstream signaling of activated FGFR3 | 18 | 2.17e-01 | 1.68e-01 | 4.34e-01 |
| Downstream signaling of activated FGFR4 | 18 | 2.17e-01 | 1.68e-01 | 4.34e-01 |
| Regulation of TLR by endogenous ligand | 11 | 3.35e-01 | -1.68e-01 | 5.53e-01 |
| SUMOylation of immune response proteins | 11 | 3.37e-01 | -1.67e-01 | 5.55e-01 |
| Elevation of cytosolic Ca2+ levels | 12 | 3.16e-01 | 1.67e-01 | 5.38e-01 |
| Vpr-mediated nuclear import of PICs | 32 | 1.03e-01 | 1.67e-01 | 2.80e-01 |
| Negative regulation of FGFR3 signaling | 22 | 1.77e-01 | -1.67e-01 | 3.82e-01 |
| Negative regulation of FGFR4 signaling | 22 | 1.77e-01 | -1.67e-01 | 3.82e-01 |
| Hedgehog ligand biogenesis | 55 | 3.33e-02 | -1.66e-01 | 1.37e-01 |
| SLC-mediated transmembrane transport | 141 | 7.17e-04 | 1.65e-01 | 9.26e-03 |
| G alpha (z) signalling events | 33 | 1.00e-01 | -1.65e-01 | 2.77e-01 |
| RNA polymerase II transcribes snRNA genes | 71 | 1.61e-02 | -1.65e-01 | 8.34e-02 |
| Interleukin-20 family signaling | 14 | 2.86e-01 | 1.65e-01 | 5.11e-01 |
| ER-Phagosome pathway | 72 | 1.58e-02 | -1.65e-01 | 8.25e-02 |
| Degradation of AXIN | 52 | 4.08e-02 | -1.64e-01 | 1.57e-01 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 13 | 3.06e-01 | -1.64e-01 | 5.30e-01 |
| RNA Polymerase II Transcription Termination | 65 | 2.24e-02 | -1.64e-01 | 1.04e-01 |
| Impaired BRCA2 binding to PALB2 | 24 | 1.65e-01 | 1.64e-01 | 3.68e-01 |
| AURKA Activation by TPX2 | 71 | 1.71e-02 | 1.64e-01 | 8.77e-02 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | 83 | 1.02e-02 | -1.63e-01 | 5.72e-02 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 25 | 1.57e-01 | -1.63e-01 | 3.61e-01 |
| Condensation of Prometaphase Chromosomes | 11 | 3.48e-01 | 1.63e-01 | 5.70e-01 |
| Sphingolipid metabolism | 71 | 1.77e-02 | 1.63e-01 | 8.99e-02 |
| Resolution of D-Loop Structures | 34 | 1.01e-01 | 1.63e-01 | 2.77e-01 |
| Switching of origins to a post-replicative state | 87 | 9.04e-03 | -1.62e-01 | 5.22e-02 |
| Interferon alpha/beta signaling | 37 | 8.88e-02 | -1.62e-01 | 2.56e-01 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 77 | 1.43e-02 | -1.62e-01 | 7.54e-02 |
| Assembly of active LPL and LIPC lipase complexes | 10 | 3.77e-01 | 1.61e-01 | 6.03e-01 |
| Interconversion of nucleotide di- and triphosphates | 25 | 1.63e-01 | 1.61e-01 | 3.67e-01 |
| Metabolism of polyamines | 55 | 3.90e-02 | -1.61e-01 | 1.53e-01 |
| Metabolism of carbohydrates | 242 | 1.86e-05 | 1.60e-01 | 4.25e-04 |
| G beta:gamma signalling through PLC beta | 13 | 3.18e-01 | -1.60e-01 | 5.38e-01 |
| Presynaptic function of Kainate receptors | 13 | 3.18e-01 | -1.60e-01 | 5.38e-01 |
| Metabolism of amino acids and derivatives | 273 | 5.92e-06 | -1.60e-01 | 1.53e-04 |
| Platelet Adhesion to exposed collagen | 10 | 3.82e-01 | 1.60e-01 | 6.05e-01 |
| Defective CFTR causes cystic fibrosis | 58 | 3.65e-02 | -1.59e-01 | 1.47e-01 |
| IRE1alpha activates chaperones | 49 | 5.47e-02 | 1.59e-01 | 1.85e-01 |
| Downstream signaling of activated FGFR2 | 21 | 2.10e-01 | 1.58e-01 | 4.25e-01 |
| Neurotransmitter release cycle | 28 | 1.49e-01 | 1.58e-01 | 3.51e-01 |
| PKMTs methylate histone lysines | 43 | 7.40e-02 | 1.58e-01 | 2.29e-01 |
| RORA activates gene expression | 17 | 2.62e-01 | 1.57e-01 | 4.87e-01 |
| Activation of SMO | 14 | 3.11e-01 | 1.56e-01 | 5.34e-01 |
| APC/C-mediated degradation of cell cycle proteins | 83 | 1.39e-02 | -1.56e-01 | 7.39e-02 |
| Regulation of mitotic cell cycle | 83 | 1.39e-02 | -1.56e-01 | 7.39e-02 |
| Signal transduction by L1 | 21 | 2.16e-01 | 1.56e-01 | 4.34e-01 |
| Signaling by Leptin | 10 | 3.93e-01 | 1.56e-01 | 6.11e-01 |
| TBC/RABGAPs | 42 | 8.03e-02 | -1.56e-01 | 2.40e-01 |
| Protein localization | 139 | 1.54e-03 | -1.56e-01 | 1.69e-02 |
| Mitochondrial biogenesis | 88 | 1.22e-02 | -1.55e-01 | 6.72e-02 |
| Nucleotide Excision Repair | 108 | 5.55e-03 | -1.55e-01 | 3.76e-02 |
| Processing of Capped Intron-Containing Pre-mRNA | 234 | 4.93e-05 | -1.55e-01 | 8.76e-04 |
| RNA Polymerase II Pre-transcription Events | 79 | 1.78e-02 | -1.54e-01 | 9.01e-02 |
| ERBB2 Activates PTK6 Signaling | 11 | 3.77e-01 | -1.54e-01 | 6.03e-01 |
| Acyl chain remodelling of PS | 12 | 3.58e-01 | -1.53e-01 | 5.81e-01 |
| Regulation of ornithine decarboxylase (ODC) | 48 | 6.63e-02 | -1.53e-01 | 2.11e-01 |
| RHO GTPases activate PAKs | 19 | 2.48e-01 | 1.53e-01 | 4.72e-01 |
| Translesion synthesis by REV1 | 16 | 2.90e-01 | -1.53e-01 | 5.16e-01 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 35 | 1.18e-01 | 1.53e-01 | 3.06e-01 |
| Downstream signaling events of B Cell Receptor (BCR) | 73 | 2.51e-02 | -1.52e-01 | 1.13e-01 |
| Pentose phosphate pathway | 14 | 3.26e-01 | 1.52e-01 | 5.46e-01 |
| Glutathione conjugation | 28 | 1.66e-01 | -1.51e-01 | 3.69e-01 |
| RHOJ GTPase cycle | 51 | 6.22e-02 | 1.51e-01 | 2.03e-01 |
| RHOU GTPase cycle | 39 | 1.03e-01 | 1.51e-01 | 2.81e-01 |
| ABC transporter disorders | 66 | 3.44e-02 | -1.51e-01 | 1.41e-01 |
| Miscellaneous transport and binding events | 22 | 2.22e-01 | 1.50e-01 | 4.39e-01 |
| Global Genome Nucleotide Excision Repair (GG-NER) | 82 | 1.87e-02 | -1.50e-01 | 9.28e-02 |
| Cargo concentration in the ER | 24 | 2.02e-01 | 1.50e-01 | 4.15e-01 |
| PINK1-PRKN Mediated Mitophagy | 18 | 2.70e-01 | -1.50e-01 | 4.94e-01 |
| ER Quality Control Compartment (ERQC) | 21 | 2.35e-01 | 1.50e-01 | 4.58e-01 |
| mRNA 3’-end processing | 56 | 5.33e-02 | -1.49e-01 | 1.83e-01 |
| Signaling by FGFR3 in disease | 15 | 3.17e-01 | 1.49e-01 | 5.38e-01 |
| Interleukin receptor SHC signaling | 16 | 3.02e-01 | 1.49e-01 | 5.29e-01 |
| Signaling by Insulin receptor | 57 | 5.20e-02 | 1.49e-01 | 1.81e-01 |
| Activation of the pre-replicative complex | 32 | 1.45e-01 | 1.49e-01 | 3.45e-01 |
| Orc1 removal from chromatin | 67 | 3.59e-02 | -1.48e-01 | 1.46e-01 |
| CaM pathway | 26 | 1.91e-01 | 1.48e-01 | 4.02e-01 |
| Calmodulin induced events | 26 | 1.91e-01 | 1.48e-01 | 4.02e-01 |
| RMTs methylate histone arginines | 33 | 1.41e-01 | -1.48e-01 | 3.39e-01 |
| TP53 Regulates Transcription of DNA Repair Genes | 61 | 4.57e-02 | -1.48e-01 | 1.66e-01 |
| Regulation of TP53 Activity through Acetylation | 29 | 1.68e-01 | -1.48e-01 | 3.72e-01 |
| Assembly of the pre-replicative complex | 87 | 1.73e-02 | -1.48e-01 | 8.82e-02 |
| Alpha-protein kinase 1 signaling pathway | 11 | 3.96e-01 | -1.48e-01 | 6.12e-01 |
| Transport of the SLBP independent Mature mRNA | 34 | 1.37e-01 | 1.48e-01 | 3.32e-01 |
| Glycogen synthesis | 12 | 3.79e-01 | -1.47e-01 | 6.04e-01 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | 12 | 3.81e-01 | 1.46e-01 | 6.05e-01 |
| Hemostasis | 410 | 4.75e-07 | 1.46e-01 | 1.51e-05 |
| VEGFR2 mediated vascular permeability | 24 | 2.16e-01 | 1.46e-01 | 4.34e-01 |
| N-glycan antennae elongation in the medial/trans-Golgi | 20 | 2.62e-01 | 1.45e-01 | 4.87e-01 |
| MECP2 regulates neuronal receptors and channels | 10 | 4.28e-01 | -1.45e-01 | 6.41e-01 |
| Pyroptosis | 17 | 3.03e-01 | -1.44e-01 | 5.29e-01 |
| Telomere Extension By Telomerase | 22 | 2.42e-01 | -1.44e-01 | 4.65e-01 |
| Sema4D induced cell migration and growth-cone collapse | 18 | 2.91e-01 | 1.44e-01 | 5.16e-01 |
| Inositol phosphate metabolism | 37 | 1.31e-01 | 1.44e-01 | 3.25e-01 |
| Signaling by high-kinase activity BRAF mutants | 30 | 1.74e-01 | 1.44e-01 | 3.79e-01 |
| Downregulation of ERBB2:ERBB3 signaling | 13 | 3.70e-01 | -1.44e-01 | 5.95e-01 |
| HCMV Early Events | 61 | 5.30e-02 | 1.43e-01 | 1.82e-01 |
| RHO GTPase Effectors | 221 | 2.66e-04 | 1.43e-01 | 3.95e-03 |
| Base-Excision Repair, AP Site Formation | 23 | 2.37e-01 | -1.42e-01 | 4.61e-01 |
| Loss of Nlp from mitotic centrosomes | 68 | 4.29e-02 | 1.42e-01 | 1.59e-01 |
| Loss of proteins required for interphase microtubule organization from the centrosome | 68 | 4.29e-02 | 1.42e-01 | 1.59e-01 |
| Regulation of RAS by GAPs | 63 | 5.27e-02 | -1.41e-01 | 1.82e-01 |
| Downstream TCR signaling | 77 | 3.24e-02 | -1.41e-01 | 1.35e-01 |
| Signaling by FGFR2 in disease | 34 | 1.55e-01 | -1.41e-01 | 3.59e-01 |
| RND3 GTPase cycle | 36 | 1.44e-01 | 1.41e-01 | 3.44e-01 |
| tRNA processing | 118 | 8.41e-03 | -1.41e-01 | 4.94e-02 |
| Myogenesis | 20 | 2.77e-01 | 1.41e-01 | 5.01e-01 |
| G1/S-Specific Transcription | 28 | 1.99e-01 | 1.40e-01 | 4.15e-01 |
| Cell death signalling via NRAGE, NRIF and NADE | 62 | 5.63e-02 | 1.40e-01 | 1.87e-01 |
| Transport of the SLBP Dependant Mature mRNA | 35 | 1.52e-01 | 1.40e-01 | 3.56e-01 |
| Glycosphingolipid metabolism | 34 | 1.58e-01 | 1.40e-01 | 3.61e-01 |
| Sensory perception of taste | 10 | 4.48e-01 | 1.39e-01 | 6.61e-01 |
| RHO GTPases Activate ROCKs | 17 | 3.22e-01 | 1.39e-01 | 5.42e-01 |
| Apoptotic cleavage of cellular proteins | 31 | 1.83e-01 | 1.38e-01 | 3.90e-01 |
| Synaptic adhesion-like molecules | 15 | 3.56e-01 | -1.38e-01 | 5.79e-01 |
| Adrenaline,noradrenaline inhibits insulin secretion | 19 | 2.99e-01 | -1.38e-01 | 5.25e-01 |
| G alpha (s) signalling events | 62 | 6.15e-02 | 1.37e-01 | 2.01e-01 |
| Processive synthesis on the C-strand of the telomere | 18 | 3.13e-01 | -1.37e-01 | 5.35e-01 |
| RHO GTPases activate PKNs | 36 | 1.54e-01 | 1.37e-01 | 3.58e-01 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 67 | 5.45e-02 | -1.36e-01 | 1.85e-01 |
| Nucleotide catabolism | 27 | 2.25e-01 | -1.35e-01 | 4.44e-01 |
| Negative regulation of FGFR2 signaling | 25 | 2.44e-01 | -1.35e-01 | 4.67e-01 |
| Cellular response to hypoxia | 69 | 5.39e-02 | -1.34e-01 | 1.83e-01 |
| EPHA-mediated growth cone collapse | 12 | 4.21e-01 | 1.34e-01 | 6.36e-01 |
| Metabolism of porphyrins | 19 | 3.12e-01 | -1.34e-01 | 5.35e-01 |
| Potassium Channels | 37 | 1.59e-01 | -1.34e-01 | 3.61e-01 |
| Heme signaling | 40 | 1.45e-01 | 1.33e-01 | 3.44e-01 |
| Signaling by NTRK2 (TRKB) | 20 | 3.04e-01 | 1.33e-01 | 5.29e-01 |
| Formation of Fibrin Clot (Clotting Cascade) | 18 | 3.30e-01 | -1.33e-01 | 5.48e-01 |
| CREB1 phosphorylation through the activation of Adenylate Cyclase | 10 | 4.70e-01 | 1.32e-01 | 6.73e-01 |
| Regulation of FZD by ubiquitination | 18 | 3.34e-01 | 1.32e-01 | 5.51e-01 |
| Cell-extracellular matrix interactions | 16 | 3.63e-01 | 1.32e-01 | 5.87e-01 |
| Glucose metabolism | 80 | 4.25e-02 | 1.31e-01 | 1.59e-01 |
| Regulation of BACH1 activity | 11 | 4.51e-01 | -1.31e-01 | 6.65e-01 |
| Signaling by FGFR2 | 61 | 7.67e-02 | -1.31e-01 | 2.34e-01 |
| Transport to the Golgi and subsequent modification | 141 | 7.86e-03 | 1.30e-01 | 4.76e-02 |
| Pyruvate metabolism | 27 | 2.43e-01 | 1.30e-01 | 4.67e-01 |
| Gluconeogenesis | 27 | 2.44e-01 | 1.30e-01 | 4.67e-01 |
| HIV Infection | 209 | 1.29e-03 | -1.30e-01 | 1.48e-02 |
| Maturation of nucleoprotein | 11 | 4.57e-01 | -1.29e-01 | 6.68e-01 |
| STING mediated induction of host immune responses | 14 | 4.03e-01 | -1.29e-01 | 6.17e-01 |
| Regulation of KIT signaling | 13 | 4.21e-01 | -1.29e-01 | 6.36e-01 |
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) | 10 | 4.81e-01 | 1.29e-01 | 6.85e-01 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | 12 | 4.41e-01 | 1.29e-01 | 6.54e-01 |
| Phosphorylation of the APC/C | 19 | 3.32e-01 | -1.28e-01 | 5.49e-01 |
| Cellular response to chemical stress | 170 | 4.01e-03 | -1.28e-01 | 3.15e-02 |
| Keratan sulfate/keratin metabolism | 26 | 2.58e-01 | 1.28e-01 | 4.84e-01 |
| Dual Incision in GG-NER | 40 | 1.61e-01 | -1.28e-01 | 3.63e-01 |
| Transcriptional Regulation by VENTX | 35 | 1.90e-01 | -1.28e-01 | 4.02e-01 |
| Gastrin-CREB signalling pathway via PKC and MAPK | 15 | 3.91e-01 | -1.28e-01 | 6.11e-01 |
| Metabolism of water-soluble vitamins and cofactors | 105 | 2.38e-02 | 1.28e-01 | 1.08e-01 |
| RAC2 GTPase cycle | 76 | 5.53e-02 | 1.27e-01 | 1.86e-01 |
| SUMOylation of transcription factors | 15 | 3.94e-01 | -1.27e-01 | 6.11e-01 |
| Transcriptional regulation by RUNX3 | 91 | 3.65e-02 | -1.27e-01 | 1.47e-01 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 27 | 2.55e-01 | 1.27e-01 | 4.82e-01 |
| Anti-inflammatory response favouring Leishmania parasite infection | 65 | 7.80e-02 | 1.27e-01 | 2.36e-01 |
| Leishmania parasite growth and survival | 65 | 7.80e-02 | 1.27e-01 | 2.36e-01 |
| SHC1 events in ERBB2 signaling | 20 | 3.29e-01 | -1.26e-01 | 5.48e-01 |
| Late Phase of HIV Life Cycle | 131 | 1.30e-02 | -1.26e-01 | 7.07e-02 |
| Initiation of Nuclear Envelope (NE) Reformation | 18 | 3.55e-01 | 1.26e-01 | 5.79e-01 |
| XBP1(S) activates chaperone genes | 47 | 1.37e-01 | 1.26e-01 | 3.32e-01 |
| Synthesis of DNA | 115 | 2.05e-02 | -1.25e-01 | 9.77e-02 |
| Signaling by RAF1 mutants | 35 | 2.00e-01 | 1.25e-01 | 4.15e-01 |
| TCR signaling | 91 | 4.04e-02 | -1.25e-01 | 1.57e-01 |
| Asymmetric localization of PCP proteins | 61 | 9.29e-02 | -1.25e-01 | 2.63e-01 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 35 | 2.05e-01 | -1.24e-01 | 4.17e-01 |
| RAC3 GTPase cycle | 79 | 5.73e-02 | 1.24e-01 | 1.88e-01 |
| Transport of Mature mRNA Derived from an Intronless Transcript | 40 | 1.76e-01 | 1.24e-01 | 3.82e-01 |
| Metabolism of vitamins and cofactors | 146 | 1.04e-02 | 1.23e-01 | 5.82e-02 |
| Cleavage of the damaged pyrimidine | 21 | 3.29e-01 | -1.23e-01 | 5.48e-01 |
| Depyrimidination | 21 | 3.29e-01 | -1.23e-01 | 5.48e-01 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 21 | 3.29e-01 | -1.23e-01 | 5.48e-01 |
| Signaling by CSF3 (G-CSF) | 26 | 2.78e-01 | -1.23e-01 | 5.03e-01 |
| Telomere C-strand (Lagging Strand) Synthesis | 33 | 2.22e-01 | -1.23e-01 | 4.39e-01 |
| Inflammasomes | 17 | 3.81e-01 | -1.23e-01 | 6.05e-01 |
| Transcriptional regulation of pluripotent stem cells | 15 | 4.11e-01 | 1.23e-01 | 6.27e-01 |
| VxPx cargo-targeting to cilium | 19 | 3.55e-01 | 1.23e-01 | 5.79e-01 |
| Cyclin D associated events in G1 | 45 | 1.56e-01 | -1.22e-01 | 3.60e-01 |
| G1 Phase | 45 | 1.56e-01 | -1.22e-01 | 3.60e-01 |
| Degradation of the extracellular matrix | 62 | 9.65e-02 | 1.22e-01 | 2.69e-01 |
| Thrombin signalling through proteinase activated receptors (PARs) | 20 | 3.48e-01 | -1.21e-01 | 5.70e-01 |
| Interleukin-12 family signaling | 41 | 1.79e-01 | 1.21e-01 | 3.86e-01 |
| Activation of NMDA receptors and postsynaptic events | 55 | 1.22e-01 | 1.21e-01 | 3.15e-01 |
| Phase I - Functionalization of compounds | 48 | 1.51e-01 | 1.20e-01 | 3.55e-01 |
| TNFR2 non-canonical NF-kB pathway | 77 | 6.98e-02 | -1.20e-01 | 2.19e-01 |
| Regulation of beta-cell development | 20 | 3.55e-01 | -1.19e-01 | 5.79e-01 |
| Cell recruitment (pro-inflammatory response) | 18 | 3.82e-01 | -1.19e-01 | 6.05e-01 |
| Purinergic signaling in leishmaniasis infection | 18 | 3.82e-01 | -1.19e-01 | 6.05e-01 |
| RHO GTPases Activate WASPs and WAVEs | 31 | 2.53e-01 | -1.19e-01 | 4.80e-01 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | 41 | 1.92e-01 | 1.18e-01 | 4.04e-01 |
| Telomere Maintenance | 70 | 8.97e-02 | -1.17e-01 | 2.57e-01 |
| Lysosome Vesicle Biogenesis | 29 | 2.74e-01 | -1.17e-01 | 4.98e-01 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 18 | 3.90e-01 | 1.17e-01 | 6.10e-01 |
| Neurexins and neuroligins | 34 | 2.38e-01 | 1.17e-01 | 4.61e-01 |
| DAP12 signaling | 20 | 3.65e-01 | 1.17e-01 | 5.90e-01 |
| The NLRP3 inflammasome | 13 | 4.66e-01 | -1.17e-01 | 6.69e-01 |
| Diseases of mitotic cell cycle | 37 | 2.19e-01 | -1.17e-01 | 4.37e-01 |
| Serotonin Neurotransmitter Release Cycle | 11 | 5.03e-01 | -1.17e-01 | 6.96e-01 |
| Regulation of PTEN stability and activity | 66 | 1.02e-01 | -1.17e-01 | 2.79e-01 |
| Signaling by TGFB family members | 104 | 4.07e-02 | 1.16e-01 | 1.57e-01 |
| RHOQ GTPase cycle | 56 | 1.33e-01 | 1.16e-01 | 3.26e-01 |
| Regulation of PTEN gene transcription | 59 | 1.24e-01 | -1.16e-01 | 3.17e-01 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 10 | 5.26e-01 | -1.16e-01 | 7.20e-01 |
| CRMPs in Sema3A signaling | 14 | 4.53e-01 | 1.16e-01 | 6.66e-01 |
| TGF-beta receptor signaling activates SMADs | 43 | 1.90e-01 | 1.16e-01 | 4.02e-01 |
| MAP2K and MAPK activation | 34 | 2.45e-01 | 1.15e-01 | 4.68e-01 |
| Pre-NOTCH Expression and Processing | 52 | 1.51e-01 | 1.15e-01 | 3.55e-01 |
| Heme biosynthesis | 12 | 4.90e-01 | -1.15e-01 | 6.92e-01 |
| Base Excision Repair | 50 | 1.60e-01 | -1.15e-01 | 3.62e-01 |
| Signaling by KIT in disease | 18 | 3.99e-01 | 1.15e-01 | 6.15e-01 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 18 | 3.99e-01 | 1.15e-01 | 6.15e-01 |
| O-linked glycosylation | 68 | 1.04e-01 | 1.14e-01 | 2.83e-01 |
| Antigen processing-Cross presentation | 78 | 8.32e-02 | -1.14e-01 | 2.47e-01 |
| Glutamate Neurotransmitter Release Cycle | 14 | 4.62e-01 | 1.14e-01 | 6.69e-01 |
| Interleukin-37 signaling | 14 | 4.63e-01 | 1.13e-01 | 6.69e-01 |
| WNT5A-dependent internalization of FZD4 | 14 | 4.63e-01 | -1.13e-01 | 6.69e-01 |
| ER to Golgi Anterograde Transport | 116 | 3.61e-02 | 1.13e-01 | 1.46e-01 |
| tRNA modification in the nucleus and cytosol | 43 | 2.01e-01 | -1.13e-01 | 4.15e-01 |
| HIV Life Cycle | 140 | 2.15e-02 | -1.13e-01 | 1.01e-01 |
| Regulation of PLK1 Activity at G2/M Transition | 86 | 7.17e-02 | 1.13e-01 | 2.24e-01 |
| Calnexin/calreticulin cycle | 26 | 3.23e-01 | 1.12e-01 | 5.42e-01 |
| Synthesis of bile acids and bile salts | 20 | 3.86e-01 | -1.12e-01 | 6.08e-01 |
| Cyclin A/B1/B2 associated events during G2/M transition | 23 | 3.55e-01 | 1.11e-01 | 5.79e-01 |
| Intra-Golgi traffic | 39 | 2.32e-01 | 1.11e-01 | 4.55e-01 |
| Activation of Matrix Metalloproteinases | 12 | 5.07e-01 | -1.11e-01 | 7.00e-01 |
| SUMOylation of SUMOylation proteins | 33 | 2.72e-01 | 1.11e-01 | 4.96e-01 |
| Dual incision in TC-NER | 64 | 1.27e-01 | -1.10e-01 | 3.21e-01 |
| Synthesis of PC | 23 | 3.60e-01 | -1.10e-01 | 5.84e-01 |
| Regulated Necrosis | 42 | 2.19e-01 | -1.10e-01 | 4.37e-01 |
| Diseases of glycosylation | 107 | 5.08e-02 | 1.10e-01 | 1.78e-01 |
| Phase II - Conjugation of compounds | 64 | 1.30e-01 | -1.09e-01 | 3.25e-01 |
| Signaling by NTRKs | 111 | 4.70e-02 | 1.09e-01 | 1.69e-01 |
| UCH proteinases | 83 | 8.64e-02 | -1.09e-01 | 2.52e-01 |
| Antiviral mechanism by IFN-stimulated genes | 71 | 1.14e-01 | 1.09e-01 | 2.98e-01 |
| Ca-dependent events | 28 | 3.20e-01 | 1.09e-01 | 5.39e-01 |
| Translesion synthesis by POLK | 17 | 4.39e-01 | -1.08e-01 | 6.53e-01 |
| CLEC7A (Dectin-1) signaling | 90 | 7.62e-02 | -1.08e-01 | 2.34e-01 |
| NOD1/2 Signaling Pathway | 27 | 3.31e-01 | 1.08e-01 | 5.48e-01 |
| GRB2 events in ERBB2 signaling | 14 | 4.84e-01 | -1.08e-01 | 6.87e-01 |
| Hyaluronan uptake and degradation | 10 | 5.56e-01 | 1.08e-01 | 7.44e-01 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 22 | 3.84e-01 | 1.07e-01 | 6.06e-01 |
| Trafficking of AMPA receptors | 22 | 3.84e-01 | 1.07e-01 | 6.06e-01 |
| ISG15 antiviral mechanism | 66 | 1.33e-01 | 1.07e-01 | 3.26e-01 |
| Signal Transduction | 1760 | 6.86e-13 | 1.07e-01 | 1.17e-10 |
| RHOH GTPase cycle | 30 | 3.13e-01 | 1.06e-01 | 5.35e-01 |
| Platelet degranulation | 94 | 7.51e-02 | 1.06e-01 | 2.31e-01 |
| Cytochrome c-mediated apoptotic response | 12 | 5.26e-01 | -1.06e-01 | 7.20e-01 |
| Regulation of insulin secretion | 49 | 2.01e-01 | 1.06e-01 | 4.15e-01 |
| Sema3A PAK dependent Axon repulsion | 16 | 4.65e-01 | -1.06e-01 | 6.69e-01 |
| NGF-stimulated transcription | 34 | 2.90e-01 | 1.05e-01 | 5.16e-01 |
| PI3K events in ERBB2 signaling | 14 | 4.98e-01 | -1.05e-01 | 6.93e-01 |
| Diseases of signal transduction by growth factor receptors and second messengers | 370 | 6.73e-04 | 1.04e-01 | 8.85e-03 |
| Neddylation | 210 | 1.02e-02 | -1.03e-01 | 5.72e-02 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 19 | 4.37e-01 | -1.03e-01 | 6.49e-01 |
| Oxidative Stress Induced Senescence | 69 | 1.40e-01 | -1.03e-01 | 3.37e-01 |
| Cell-cell junction organization | 32 | 3.14e-01 | -1.03e-01 | 5.36e-01 |
| Transcriptional regulation by RUNX2 | 106 | 6.79e-02 | -1.03e-01 | 2.14e-01 |
| Deactivation of the beta-catenin transactivating complex | 38 | 2.74e-01 | -1.03e-01 | 4.98e-01 |
| Meiotic synapsis | 31 | 3.23e-01 | 1.03e-01 | 5.42e-01 |
| Erythropoietin activates RAS | 12 | 5.40e-01 | 1.02e-01 | 7.30e-01 |
| SUMOylation | 157 | 2.80e-02 | 1.02e-01 | 1.22e-01 |
| DNA Replication Pre-Initiation | 103 | 7.48e-02 | -1.02e-01 | 2.31e-01 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 21 | 4.20e-01 | 1.02e-01 | 6.36e-01 |
| Signaling by NODAL | 13 | 5.26e-01 | -1.02e-01 | 7.20e-01 |
| Integration of energy metabolism | 74 | 1.32e-01 | 1.01e-01 | 3.25e-01 |
| PCP/CE pathway | 85 | 1.07e-01 | -1.01e-01 | 2.88e-01 |
| Peroxisomal protein import | 52 | 2.09e-01 | -1.01e-01 | 4.25e-01 |
| MHC class II antigen presentation | 81 | 1.18e-01 | 1.01e-01 | 3.06e-01 |
| Processive synthesis on the lagging strand | 14 | 5.15e-01 | 1.00e-01 | 7.09e-01 |
| Protein folding | 78 | 1.28e-01 | -9.98e-02 | 3.22e-01 |
| Plasma lipoprotein assembly, remodeling, and clearance | 52 | 2.16e-01 | 9.92e-02 | 4.34e-01 |
| Ca2+ pathway | 51 | 2.21e-01 | 9.92e-02 | 4.39e-01 |
| PTEN Regulation | 136 | 4.69e-02 | -9.89e-02 | 1.69e-01 |
| Chromosome Maintenance | 95 | 9.79e-02 | -9.84e-02 | 2.72e-01 |
| Paracetamol ADME | 17 | 4.83e-01 | -9.83e-02 | 6.87e-01 |
| Metabolic disorders of biological oxidation enzymes | 19 | 4.59e-01 | -9.81e-02 | 6.69e-01 |
| Regulation of TP53 Activity through Methylation | 17 | 4.84e-01 | -9.81e-02 | 6.87e-01 |
| Response to elevated platelet cytosolic Ca2+ | 98 | 9.65e-02 | 9.73e-02 | 2.69e-01 |
| Nuclear Envelope (NE) Reassembly | 65 | 1.75e-01 | 9.73e-02 | 3.82e-01 |
| NOTCH1 Intracellular Domain Regulates Transcription | 46 | 2.55e-01 | -9.71e-02 | 4.82e-01 |
| MicroRNA (miRNA) biogenesis | 24 | 4.11e-01 | -9.70e-02 | 6.27e-01 |
| COPI-mediated anterograde transport | 72 | 1.55e-01 | 9.70e-02 | 3.59e-01 |
| Interleukin-2 family signaling | 27 | 3.84e-01 | 9.68e-02 | 6.06e-01 |
| Killing mechanisms | 10 | 5.97e-01 | -9.66e-02 | 7.70e-01 |
| WNT5:FZD7-mediated leishmania damping | 10 | 5.97e-01 | -9.66e-02 | 7.70e-01 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 37 | 3.10e-01 | 9.66e-02 | 5.34e-01 |
| Signaling by RAS mutants | 37 | 3.10e-01 | 9.66e-02 | 5.34e-01 |
| Signaling by moderate kinase activity BRAF mutants | 37 | 3.10e-01 | 9.66e-02 | 5.34e-01 |
| Signaling downstream of RAS mutants | 37 | 3.10e-01 | 9.66e-02 | 5.34e-01 |
| Chaperonin-mediated protein folding | 72 | 1.58e-01 | -9.63e-02 | 3.61e-01 |
| Mitotic Prophase | 84 | 1.29e-01 | 9.61e-02 | 3.23e-01 |
| G beta:gamma signalling through PI3Kgamma | 17 | 4.94e-01 | -9.58e-02 | 6.93e-01 |
| Long-term potentiation | 14 | 5.36e-01 | 9.57e-02 | 7.27e-01 |
| G0 and Early G1 | 26 | 4.00e-01 | 9.53e-02 | 6.15e-01 |
| Plasma lipoprotein remodeling | 18 | 4.84e-01 | 9.53e-02 | 6.87e-01 |
| The role of Nef in HIV-1 replication and disease pathogenesis | 20 | 4.61e-01 | -9.53e-02 | 6.69e-01 |
| Cytosolic iron-sulfur cluster assembly | 13 | 5.53e-01 | -9.49e-02 | 7.42e-01 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 24 | 4.21e-01 | -9.49e-02 | 6.36e-01 |
| activated TAK1 mediates p38 MAPK activation | 18 | 4.87e-01 | -9.47e-02 | 6.89e-01 |
| NOTCH3 Intracellular Domain Regulates Transcription | 20 | 4.67e-01 | -9.40e-02 | 6.70e-01 |
| DNA strand elongation | 31 | 3.66e-01 | 9.40e-02 | 5.90e-01 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | 24 | 4.27e-01 | -9.37e-02 | 6.41e-01 |
| Transferrin endocytosis and recycling | 25 | 4.18e-01 | 9.36e-02 | 6.34e-01 |
| Autophagy | 118 | 7.98e-02 | -9.35e-02 | 2.40e-01 |
| Synthesis of glycosylphosphatidylinositol (GPI) | 17 | 5.06e-01 | -9.31e-02 | 7.00e-01 |
| PPARA activates gene expression | 101 | 1.08e-01 | 9.27e-02 | 2.89e-01 |
| Josephin domain DUBs | 11 | 5.95e-01 | -9.26e-02 | 7.69e-01 |
| TRP channels | 10 | 6.13e-01 | 9.25e-02 | 7.82e-01 |
| Phase 0 - rapid depolarisation | 13 | 5.64e-01 | -9.24e-02 | 7.48e-01 |
| InlB-mediated entry of Listeria monocytogenes into host cell | 14 | 5.51e-01 | -9.22e-02 | 7.40e-01 |
| C-type lectin receptors (CLRs) | 108 | 9.90e-02 | -9.21e-02 | 2.75e-01 |
| HSF1 activation | 25 | 4.26e-01 | -9.20e-02 | 6.41e-01 |
| Interleukin-6 family signaling | 20 | 4.78e-01 | 9.18e-02 | 6.83e-01 |
| Regulation of Complement cascade | 20 | 4.79e-01 | -9.16e-02 | 6.83e-01 |
| Disorders of Developmental Biology | 12 | 5.84e-01 | -9.14e-02 | 7.58e-01 |
| Disorders of Nervous System Development | 12 | 5.84e-01 | -9.14e-02 | 7.58e-01 |
| Loss of function of MECP2 in Rett syndrome | 12 | 5.84e-01 | -9.14e-02 | 7.58e-01 |
| Pervasive developmental disorders | 12 | 5.84e-01 | -9.14e-02 | 7.58e-01 |
| SUMO E3 ligases SUMOylate target proteins | 151 | 5.35e-02 | 9.13e-02 | 1.83e-01 |
| DAP12 interactions | 22 | 4.59e-01 | 9.12e-02 | 6.69e-01 |
| TP53 Regulates Metabolic Genes | 84 | 1.51e-01 | -9.08e-02 | 3.55e-01 |
| Transcriptional Regulation by MECP2 | 44 | 2.98e-01 | 9.07e-02 | 5.25e-01 |
| Fcgamma receptor (FCGR) dependent phagocytosis | 71 | 1.88e-01 | 9.06e-02 | 3.98e-01 |
| ERBB2 Regulates Cell Motility | 13 | 5.74e-01 | -9.01e-02 | 7.54e-01 |
| DNA Replication | 128 | 7.94e-02 | -9.00e-02 | 2.40e-01 |
| MAPK targets/ Nuclear events mediated by MAP kinases | 30 | 3.94e-01 | -8.99e-02 | 6.11e-01 |
| Purine catabolism | 15 | 5.47e-01 | -8.97e-02 | 7.36e-01 |
| Constitutive Signaling by Overexpressed ERBB2 | 11 | 6.07e-01 | 8.96e-02 | 7.77e-01 |
| FOXO-mediated transcription of cell cycle genes | 16 | 5.36e-01 | 8.95e-02 | 7.27e-01 |
| Nuclear signaling by ERBB4 | 25 | 4.40e-01 | -8.92e-02 | 6.53e-01 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 23 | 4.61e-01 | -8.89e-02 | 6.69e-01 |
| Receptor-type tyrosine-protein phosphatases | 10 | 6.27e-01 | 8.88e-02 | 7.84e-01 |
| Negative regulation of FGFR1 signaling | 24 | 4.52e-01 | -8.88e-02 | 6.65e-01 |
| FCGR3A-mediated phagocytosis | 48 | 2.91e-01 | 8.81e-02 | 5.16e-01 |
| Leishmania phagocytosis | 48 | 2.91e-01 | 8.81e-02 | 5.16e-01 |
| Parasite infection | 48 | 2.91e-01 | 8.81e-02 | 5.16e-01 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 40 | 3.40e-01 | 8.72e-02 | 5.59e-01 |
| Metabolism of lipids | 555 | 5.14e-04 | 8.71e-02 | 6.89e-03 |
| Recruitment of NuMA to mitotic centrosomes | 79 | 1.82e-01 | 8.70e-02 | 3.89e-01 |
| Cell-Cell communication | 83 | 1.71e-01 | 8.70e-02 | 3.76e-01 |
| Platelet activation, signaling and aggregation | 185 | 4.23e-02 | 8.68e-02 | 1.59e-01 |
| Suppression of phagosomal maturation | 11 | 6.20e-01 | -8.64e-02 | 7.83e-01 |
| Methylation | 11 | 6.21e-01 | -8.62e-02 | 7.83e-01 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 29 | 4.22e-01 | 8.61e-02 | 6.36e-01 |
| Signaling by TGF-beta Receptor Complex | 87 | 1.66e-01 | 8.61e-02 | 3.69e-01 |
| Asparagine N-linked glycosylation | 248 | 2.03e-02 | 8.60e-02 | 9.74e-02 |
| RIPK1-mediated regulated necrosis | 25 | 4.57e-01 | -8.60e-02 | 6.68e-01 |
| Regulation of necroptotic cell death | 25 | 4.57e-01 | -8.60e-02 | 6.68e-01 |
| Fc epsilon receptor (FCERI) signaling | 116 | 1.11e-01 | -8.59e-02 | 2.93e-01 |
| RNA Polymerase II Transcription | 974 | 8.40e-06 | -8.59e-02 | 1.98e-04 |
| Cellular Senescence | 132 | 8.96e-02 | -8.58e-02 | 2.57e-01 |
| Constitutive Signaling by EGFRvIII | 15 | 5.66e-01 | 8.57e-02 | 7.48e-01 |
| Signaling by EGFRvIII in Cancer | 15 | 5.66e-01 | 8.57e-02 | 7.48e-01 |
| Signaling by GPCR | 286 | 1.32e-02 | 8.56e-02 | 7.10e-02 |
| EPHB-mediated forward signaling | 32 | 4.03e-01 | 8.55e-02 | 6.17e-01 |
| CD209 (DC-SIGN) signaling | 18 | 5.30e-01 | -8.55e-02 | 7.23e-01 |
| Pre-NOTCH Transcription and Translation | 39 | 3.58e-01 | 8.51e-02 | 5.81e-01 |
| Regulation of pyruvate dehydrogenase (PDH) complex | 15 | 5.69e-01 | 8.50e-02 | 7.50e-01 |
| Interleukin-1 signaling | 102 | 1.41e-01 | -8.44e-02 | 3.40e-01 |
| Signal regulatory protein family interactions | 10 | 6.44e-01 | -8.43e-02 | 7.98e-01 |
| p75 NTR receptor-mediated signalling | 79 | 1.96e-01 | 8.43e-02 | 4.11e-01 |
| Regulation of MECP2 expression and activity | 29 | 4.33e-01 | 8.41e-02 | 6.47e-01 |
| Signaling by FGFR | 70 | 2.26e-01 | -8.37e-02 | 4.45e-01 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 22 | 4.98e-01 | 8.36e-02 | 6.93e-01 |
| Transcriptional Regulation by E2F6 | 34 | 4.00e-01 | 8.35e-02 | 6.15e-01 |
| Positive epigenetic regulation of rRNA expression | 53 | 2.94e-01 | -8.34e-02 | 5.20e-01 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 16 | 5.64e-01 | -8.33e-02 | 7.48e-01 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | 63 | 2.53e-01 | -8.33e-02 | 4.80e-01 |
| EGFR downregulation | 27 | 4.54e-01 | -8.32e-02 | 6.67e-01 |
| Activation of ATR in response to replication stress | 37 | 3.83e-01 | 8.30e-02 | 6.06e-01 |
| Golgi Associated Vesicle Biogenesis | 51 | 3.07e-01 | 8.27e-02 | 5.32e-01 |
| Centrosome maturation | 80 | 2.02e-01 | 8.27e-02 | 4.15e-01 |
| Recruitment of mitotic centrosome proteins and complexes | 80 | 2.02e-01 | 8.27e-02 | 4.15e-01 |
| HDR through MMEJ (alt-NHEJ) | 12 | 6.20e-01 | -8.26e-02 | 7.83e-01 |
| Interleukin-4 and Interleukin-13 signaling | 73 | 2.23e-01 | 8.25e-02 | 4.41e-01 |
| Endogenous sterols | 17 | 5.56e-01 | 8.25e-02 | 7.44e-01 |
| IRAK1 recruits IKK complex | 10 | 6.52e-01 | 8.24e-02 | 8.03e-01 |
| IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | 10 | 6.52e-01 | 8.24e-02 | 8.03e-01 |
| GPER1 signaling | 32 | 4.21e-01 | 8.22e-02 | 6.36e-01 |
| Death Receptor Signalling | 118 | 1.24e-01 | 8.21e-02 | 3.17e-01 |
| Signaling by NTRK1 (TRKA) | 98 | 1.61e-01 | 8.21e-02 | 3.63e-01 |
| Signaling by EGFR in Cancer | 22 | 5.06e-01 | -8.20e-02 | 7.00e-01 |
| mRNA decay by 3’ to 5’ exoribonuclease | 15 | 5.83e-01 | -8.19e-02 | 7.58e-01 |
| Regulation of lipid metabolism by PPARalpha | 103 | 1.52e-01 | 8.18e-02 | 3.56e-01 |
| Resolution of Abasic Sites (AP sites) | 37 | 3.94e-01 | -8.11e-02 | 6.11e-01 |
| PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 14 | 6.00e-01 | 8.09e-02 | 7.72e-01 |
| Processing of Capped Intronless Pre-mRNA | 28 | 4.60e-01 | -8.08e-02 | 6.69e-01 |
| Generic Transcription Pathway | 856 | 8.40e-05 | -8.04e-02 | 1.42e-03 |
| S Phase | 157 | 8.35e-02 | -8.03e-02 | 2.47e-01 |
| SHC-mediated cascade:FGFR2 | 14 | 6.03e-01 | 8.03e-02 | 7.75e-01 |
| Impaired BRCA2 binding to RAD51 | 35 | 4.15e-01 | 7.97e-02 | 6.32e-01 |
| Biotin transport and metabolism | 11 | 6.47e-01 | 7.97e-02 | 8.01e-01 |
| GPCR downstream signalling | 257 | 2.87e-02 | 7.96e-02 | 1.24e-01 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 97 | 1.77e-01 | -7.94e-02 | 3.82e-01 |
| Toll Like Receptor 2 (TLR2) Cascade | 97 | 1.77e-01 | -7.94e-02 | 3.82e-01 |
| Toll Like Receptor TLR1:TLR2 Cascade | 97 | 1.77e-01 | -7.94e-02 | 3.82e-01 |
| Toll Like Receptor TLR6:TLR2 Cascade | 97 | 1.77e-01 | -7.94e-02 | 3.82e-01 |
| Removal of the Flap Intermediate | 13 | 6.21e-01 | 7.92e-02 | 7.83e-01 |
| Leading Strand Synthesis | 13 | 6.21e-01 | -7.92e-02 | 7.83e-01 |
| Polymerase switching | 13 | 6.21e-01 | -7.92e-02 | 7.83e-01 |
| Negative regulation of the PI3K/AKT network | 81 | 2.19e-01 | 7.91e-02 | 4.37e-01 |
| Transport of small molecules | 462 | 3.95e-03 | 7.89e-02 | 3.12e-02 |
| Circadian Clock | 63 | 2.80e-01 | 7.88e-02 | 5.05e-01 |
| RAB geranylgeranylation | 51 | 3.31e-01 | -7.88e-02 | 5.48e-01 |
| ROS and RNS production in phagocytes | 21 | 5.32e-01 | -7.87e-02 | 7.25e-01 |
| Selective autophagy | 54 | 3.19e-01 | -7.85e-02 | 5.39e-01 |
| Ovarian tumor domain proteases | 33 | 4.36e-01 | 7.84e-02 | 6.49e-01 |
| Detoxification of Reactive Oxygen Species | 28 | 4.82e-01 | -7.69e-02 | 6.86e-01 |
| Negative regulators of DDX58/IFIH1 signaling | 29 | 4.75e-01 | -7.67e-02 | 6.80e-01 |
| Glycerophospholipid biosynthesis | 92 | 2.06e-01 | -7.65e-02 | 4.18e-01 |
| COPII-mediated vesicle transport | 59 | 3.10e-01 | 7.64e-02 | 5.34e-01 |
| Gene expression (Transcription) | 1096 | 3.10e-05 | -7.61e-02 | 6.42e-04 |
| Deadenylation-dependent mRNA decay | 51 | 3.48e-01 | -7.61e-02 | 5.70e-01 |
| RHOBTB2 GTPase cycle | 23 | 5.29e-01 | 7.58e-02 | 7.23e-01 |
| Homologous DNA Pairing and Strand Exchange | 43 | 3.90e-01 | 7.58e-02 | 6.10e-01 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 44 | 3.85e-01 | -7.57e-02 | 6.07e-01 |
| Host Interactions of HIV factors | 115 | 1.62e-01 | -7.56e-02 | 3.65e-01 |
| Synthesis of substrates in N-glycan biosythesis | 52 | 3.46e-01 | -7.56e-02 | 5.69e-01 |
| Hedgehog ‘on’ state | 75 | 2.59e-01 | -7.55e-02 | 4.84e-01 |
| Downregulation of ERBB2 signaling | 27 | 4.98e-01 | -7.54e-02 | 6.93e-01 |
| SHC-mediated cascade:FGFR3 | 11 | 6.66e-01 | 7.52e-02 | 8.09e-01 |
| SHC-mediated cascade:FGFR4 | 11 | 6.66e-01 | 7.52e-02 | 8.09e-01 |
| Interleukin-12 signaling | 35 | 4.43e-01 | 7.50e-02 | 6.55e-01 |
| Triglyceride catabolism | 13 | 6.41e-01 | 7.48e-02 | 7.96e-01 |
| Activation of kainate receptors upon glutamate binding | 21 | 5.53e-01 | -7.47e-02 | 7.42e-01 |
| Metabolism of nitric oxide: NOS3 activation and regulation | 12 | 6.55e-01 | -7.44e-02 | 8.04e-01 |
| RUNX2 regulates bone development | 26 | 5.13e-01 | 7.41e-02 | 7.07e-01 |
| Defective pyroptosis | 20 | 5.66e-01 | 7.41e-02 | 7.49e-01 |
| Translation of Structural Proteins | 28 | 4.99e-01 | -7.39e-02 | 6.93e-01 |
| Rap1 signalling | 12 | 6.59e-01 | 7.37e-02 | 8.04e-01 |
| Nuclear events mediated by NFE2L2 | 74 | 2.74e-01 | -7.36e-02 | 4.98e-01 |
| Blood group systems biosynthesis | 10 | 6.87e-01 | 7.35e-02 | 8.22e-01 |
| Lewis blood group biosynthesis | 10 | 6.87e-01 | 7.35e-02 | 8.22e-01 |
| RHOBTB1 GTPase cycle | 23 | 5.43e-01 | -7.33e-02 | 7.33e-01 |
| Membrane Trafficking | 525 | 4.52e-03 | 7.31e-02 | 3.38e-02 |
| Signaling by NOTCH3 | 42 | 4.18e-01 | -7.24e-02 | 6.34e-01 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 17 | 6.06e-01 | -7.23e-02 | 7.76e-01 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 47 | 3.94e-01 | 7.19e-02 | 6.11e-01 |
| trans-Golgi Network Vesicle Budding | 65 | 3.17e-01 | 7.18e-02 | 5.38e-01 |
| N-Glycan antennae elongation | 13 | 6.54e-01 | -7.17e-02 | 8.04e-01 |
| Beta-oxidation of very long chain fatty acids | 11 | 6.81e-01 | -7.15e-02 | 8.18e-01 |
| Glycogen breakdown (glycogenolysis) | 12 | 6.69e-01 | 7.14e-02 | 8.12e-01 |
| Protein-protein interactions at synapses | 52 | 3.74e-01 | 7.14e-02 | 5.99e-01 |
| Signaling by FGFR4 | 32 | 4.85e-01 | -7.13e-02 | 6.88e-01 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | 22 | 5.63e-01 | -7.12e-02 | 7.48e-01 |
| Aggrephagy | 20 | 5.83e-01 | -7.10e-02 | 7.58e-01 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 71 | 3.03e-01 | -7.07e-02 | 5.29e-01 |
| Negative regulation of MAPK pathway | 42 | 4.28e-01 | 7.07e-02 | 6.41e-01 |
| Processing of SMDT1 | 14 | 6.48e-01 | -7.05e-02 | 8.01e-01 |
| ERK/MAPK targets | 21 | 5.76e-01 | -7.04e-02 | 7.56e-01 |
| Vesicle-mediated transport | 549 | 5.33e-03 | 7.02e-02 | 3.63e-02 |
| Neurotransmitter receptors and postsynaptic signal transmission | 105 | 2.16e-01 | 7.01e-02 | 4.34e-01 |
| E2F mediated regulation of DNA replication | 21 | 5.78e-01 | -7.01e-02 | 7.57e-01 |
| Late SARS-CoV-2 Infection Events | 55 | 3.69e-01 | 7.00e-02 | 5.94e-01 |
| Regulation of actin dynamics for phagocytic cup formation | 50 | 3.92e-01 | 7.00e-02 | 6.11e-01 |
| PCNA-Dependent Long Patch Base Excision Repair | 20 | 5.89e-01 | -6.99e-02 | 7.62e-01 |
| Pexophagy | 10 | 7.03e-01 | -6.97e-02 | 8.29e-01 |
| GABA receptor activation | 28 | 5.25e-01 | -6.95e-02 | 7.20e-01 |
| Post NMDA receptor activation events | 46 | 4.15e-01 | 6.95e-02 | 6.32e-01 |
| MyD88-independent TLR4 cascade | 99 | 2.34e-01 | -6.94e-02 | 4.57e-01 |
| TRIF(TICAM1)-mediated TLR4 signaling | 99 | 2.34e-01 | -6.94e-02 | 4.57e-01 |
| SUMOylation of ubiquitinylation proteins | 38 | 4.60e-01 | 6.93e-02 | 6.69e-01 |
| Translation of Replicase and Assembly of the Replication Transcription Complex | 11 | 6.91e-01 | 6.92e-02 | 8.23e-01 |
| Signaling by FGFR3 | 33 | 4.94e-01 | -6.89e-02 | 6.93e-01 |
| Clathrin-mediated endocytosis | 117 | 1.99e-01 | 6.89e-02 | 4.15e-01 |
| Metalloprotease DUBs | 17 | 6.26e-01 | -6.82e-02 | 7.84e-01 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 23 | 5.72e-01 | -6.81e-02 | 7.52e-01 |
| Gene Silencing by RNA | 72 | 3.18e-01 | 6.81e-02 | 5.38e-01 |
| Diseases associated with glycosylation precursor biosynthesis | 15 | 6.49e-01 | 6.80e-02 | 8.01e-01 |
| NOTCH4 Intracellular Domain Regulates Transcription | 18 | 6.18e-01 | -6.79e-02 | 7.83e-01 |
| Interleukin-10 signaling | 18 | 6.20e-01 | 6.76e-02 | 7.83e-01 |
| Retrograde transport at the Trans-Golgi-Network | 47 | 4.23e-01 | 6.76e-02 | 6.37e-01 |
| Transcriptional Regulation by TP53 | 339 | 3.44e-02 | -6.73e-02 | 1.41e-01 |
| Notch-HLH transcription pathway | 27 | 5.46e-01 | -6.72e-02 | 7.36e-01 |
| Developmental Biology | 661 | 3.62e-03 | -6.72e-02 | 2.94e-02 |
| Toll Like Receptor 3 (TLR3) Cascade | 96 | 2.57e-01 | -6.70e-02 | 4.84e-01 |
| TNFR1-induced NFkappaB signaling pathway | 25 | 5.63e-01 | 6.69e-02 | 7.48e-01 |
| MyD88 dependent cascade initiated on endosome | 92 | 2.68e-01 | -6.69e-02 | 4.92e-01 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 92 | 2.68e-01 | -6.69e-02 | 4.92e-01 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 91 | 2.72e-01 | -6.68e-02 | 4.96e-01 |
| MAP kinase activation | 61 | 3.67e-01 | -6.68e-02 | 5.92e-01 |
| Reproduction | 60 | 3.74e-01 | 6.64e-02 | 5.99e-01 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 26 | 5.59e-01 | -6.62e-02 | 7.47e-01 |
| Mitotic Metaphase and Anaphase | 216 | 9.50e-02 | 6.62e-02 | 2.67e-01 |
| GRB2 events in EGFR signaling | 10 | 7.17e-01 | -6.62e-02 | 8.38e-01 |
| Norepinephrine Neurotransmitter Release Cycle | 10 | 7.17e-01 | -6.61e-02 | 8.38e-01 |
| Toll Like Receptor 4 (TLR4) Cascade | 120 | 2.13e-01 | -6.60e-02 | 4.31e-01 |
| Anchoring of the basal body to the plasma membrane | 96 | 2.66e-01 | 6.58e-02 | 4.89e-01 |
| Transport of Mature Transcript to Cytoplasm | 79 | 3.13e-01 | -6.58e-02 | 5.35e-01 |
| Insulin processing | 22 | 5.94e-01 | 6.57e-02 | 7.69e-01 |
| Regulation of HSF1-mediated heat shock response | 76 | 3.25e-01 | 6.54e-02 | 5.44e-01 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants | 13 | 6.84e-01 | -6.53e-02 | 8.20e-01 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer | 13 | 6.84e-01 | -6.53e-02 | 8.20e-01 |
| FCERI mediated MAPK activation | 26 | 5.66e-01 | -6.51e-02 | 7.48e-01 |
| Mitotic Anaphase | 215 | 1.01e-01 | 6.51e-02 | 2.79e-01 |
| Diseases of metabolism | 181 | 1.33e-01 | 6.49e-02 | 3.26e-01 |
| Sensory Perception | 194 | 1.21e-01 | -6.48e-02 | 3.13e-01 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 19 | 6.26e-01 | -6.47e-02 | 7.84e-01 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 19 | 6.26e-01 | -6.47e-02 | 7.84e-01 |
| VEGFA-VEGFR2 Pathway | 81 | 3.17e-01 | 6.45e-02 | 5.38e-01 |
| Leishmania infection | 133 | 2.01e-01 | 6.43e-02 | 4.15e-01 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 67 | 3.65e-01 | -6.41e-02 | 5.90e-01 |
| Formation of apoptosome | 10 | 7.26e-01 | -6.40e-02 | 8.42e-01 |
| Regulation of the apoptosome activity | 10 | 7.26e-01 | -6.40e-02 | 8.42e-01 |
| Prolactin receptor signaling | 12 | 7.01e-01 | -6.40e-02 | 8.29e-01 |
| Gap junction trafficking and regulation | 15 | 6.70e-01 | 6.36e-02 | 8.12e-01 |
| Mitochondrial tRNA aminoacylation | 21 | 6.14e-01 | 6.36e-02 | 7.83e-01 |
| DNA Double Strand Break Response | 45 | 4.62e-01 | -6.35e-02 | 6.69e-01 |
| Vitamin B5 (pantothenate) metabolism | 16 | 6.62e-01 | 6.31e-02 | 8.07e-01 |
| Pyruvate metabolism and Citric Acid (TCA) cycle | 51 | 4.37e-01 | 6.30e-02 | 6.49e-01 |
| Signaling by the B Cell Receptor (BCR) | 93 | 2.95e-01 | -6.30e-02 | 5.20e-01 |
| Nonhomologous End-Joining (NHEJ) | 35 | 5.21e-01 | 6.28e-02 | 7.15e-01 |
| Separation of Sister Chromatids | 163 | 1.69e-01 | 6.27e-02 | 3.72e-01 |
| Cytosolic sensors of pathogen-associated DNA | 59 | 4.07e-01 | -6.25e-02 | 6.22e-01 |
| PRC2 methylates histones and DNA | 20 | 6.29e-01 | 6.25e-02 | 7.85e-01 |
| Activation of RAC1 | 11 | 7.22e-01 | -6.21e-02 | 8.41e-01 |
| SUMOylation of intracellular receptors | 22 | 6.16e-01 | -6.18e-02 | 7.83e-01 |
| Complement cascade | 22 | 6.17e-01 | -6.17e-02 | 7.83e-01 |
| Purine salvage | 12 | 7.12e-01 | -6.16e-02 | 8.35e-01 |
| KEAP1-NFE2L2 pathway | 94 | 3.03e-01 | -6.15e-02 | 5.29e-01 |
| SHC1 events in EGFR signaling | 11 | 7.24e-01 | -6.14e-02 | 8.42e-01 |
| Chemokine receptors bind chemokines | 13 | 7.02e-01 | -6.14e-02 | 8.29e-01 |
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 41 | 4.97e-01 | 6.13e-02 | 6.93e-01 |
| Diseases of DNA Double-Strand Break Repair | 41 | 4.97e-01 | 6.13e-02 | 6.93e-01 |
| DARPP-32 events | 22 | 6.20e-01 | -6.11e-02 | 7.83e-01 |
| Termination of translesion DNA synthesis | 31 | 5.57e-01 | -6.10e-02 | 7.44e-01 |
| Scavenging by Class A Receptors | 14 | 6.93e-01 | 6.10e-02 | 8.24e-01 |
| Rab regulation of trafficking | 114 | 2.64e-01 | -6.07e-02 | 4.88e-01 |
| Assembly of the ORC complex at the origin of replication | 16 | 6.75e-01 | -6.06e-02 | 8.13e-01 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | 12 | 7.17e-01 | 6.05e-02 | 8.38e-01 |
| Meiosis | 53 | 4.47e-01 | 6.05e-02 | 6.61e-01 |
| Extension of Telomeres | 49 | 4.65e-01 | -6.04e-02 | 6.69e-01 |
| DNA Damage Bypass | 46 | 4.79e-01 | 6.03e-02 | 6.84e-01 |
| Transcriptional regulation by RUNX1 | 155 | 1.97e-01 | -6.02e-02 | 4.12e-01 |
| Ephrin signaling | 18 | 6.58e-01 | -6.02e-02 | 8.04e-01 |
| Caspase activation via Death Receptors in the presence of ligand | 12 | 7.18e-01 | -6.02e-02 | 8.38e-01 |
| G1/S Transition | 126 | 2.46e-01 | -6.00e-02 | 4.70e-01 |
| Cell Cycle, Mitotic | 478 | 2.62e-02 | 5.99e-02 | 1.16e-01 |
| Nucleotide salvage | 21 | 6.35e-01 | -5.98e-02 | 7.91e-01 |
| Regulation of FOXO transcriptional activity by acetylation | 10 | 7.44e-01 | 5.97e-02 | 8.52e-01 |
| Deubiquitination | 225 | 1.26e-01 | 5.95e-02 | 3.18e-01 |
| Sema4D in semaphorin signaling | 22 | 6.30e-01 | 5.94e-02 | 7.86e-01 |
| Epigenetic regulation of gene expression | 94 | 3.20e-01 | -5.94e-02 | 5.40e-01 |
| Arachidonic acid metabolism | 29 | 5.80e-01 | 5.94e-02 | 7.58e-01 |
| Post-translational protein modification | 1102 | 1.15e-03 | 5.92e-02 | 1.41e-02 |
| M Phase | 339 | 6.35e-02 | 5.90e-02 | 2.06e-01 |
| RAF activation | 32 | 5.64e-01 | 5.89e-02 | 7.48e-01 |
| AKT phosphorylates targets in the cytosol | 14 | 7.04e-01 | -5.86e-02 | 8.29e-01 |
| EPH-ephrin mediated repulsion of cells | 42 | 5.13e-01 | -5.85e-02 | 7.06e-01 |
| Meiotic recombination | 29 | 5.87e-01 | 5.84e-02 | 7.61e-01 |
| RET signaling | 30 | 5.84e-01 | 5.78e-02 | 7.58e-01 |
| Extra-nuclear estrogen signaling | 57 | 4.51e-01 | 5.78e-02 | 6.65e-01 |
| Chromatin modifying enzymes | 203 | 1.58e-01 | 5.77e-02 | 3.61e-01 |
| Chromatin organization | 203 | 1.58e-01 | 5.77e-02 | 3.61e-01 |
| Macroautophagy | 106 | 3.06e-01 | -5.77e-02 | 5.30e-01 |
| Ion transport by P-type ATPases | 28 | 5.98e-01 | 5.77e-02 | 7.70e-01 |
| Presynaptic phase of homologous DNA pairing and strand exchange | 40 | 5.30e-01 | 5.74e-02 | 7.23e-01 |
| Translesion Synthesis by POLH | 18 | 6.74e-01 | -5.73e-02 | 8.12e-01 |
| NOTCH2 intracellular domain regulates transcription | 10 | 7.55e-01 | 5.70e-02 | 8.57e-01 |
| Ion homeostasis | 29 | 5.96e-01 | -5.69e-02 | 7.70e-01 |
| FOXO-mediated transcription of cell death genes | 15 | 7.04e-01 | 5.67e-02 | 8.29e-01 |
| Formation of the beta-catenin:TCF transactivating complex | 38 | 5.47e-01 | 5.65e-02 | 7.36e-01 |
| Branched-chain amino acid catabolism | 21 | 6.55e-01 | -5.64e-02 | 8.04e-01 |
| Semaphorin interactions | 56 | 4.66e-01 | 5.64e-02 | 6.69e-01 |
| HDR through Homologous Recombination (HRR) | 66 | 4.29e-01 | 5.64e-02 | 6.41e-01 |
| Regulation of TP53 Degradation | 34 | 5.71e-01 | -5.62e-02 | 7.51e-01 |
| Regulation of TP53 Expression and Degradation | 34 | 5.71e-01 | -5.62e-02 | 7.51e-01 |
| Ras activation upon Ca2+ influx through NMDA receptor | 15 | 7.06e-01 | 5.62e-02 | 8.31e-01 |
| Axon guidance | 416 | 5.13e-02 | -5.61e-02 | 1.79e-01 |
| Neutrophil degranulation | 334 | 8.00e-02 | 5.61e-02 | 2.40e-01 |
| Transcriptional regulation of granulopoiesis | 30 | 6.00e-01 | 5.53e-02 | 7.72e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 13 | 7.33e-01 | 5.47e-02 | 8.45e-01 |
| Glucagon signaling in metabolic regulation | 22 | 6.58e-01 | 5.46e-02 | 8.04e-01 |
| Dopamine Neurotransmitter Release Cycle | 14 | 7.25e-01 | 5.44e-02 | 8.42e-01 |
| Cellular responses to stress | 636 | 2.16e-02 | -5.40e-02 | 1.01e-01 |
| ADORA2B mediated anti-inflammatory cytokines production | 44 | 5.36e-01 | 5.39e-02 | 7.27e-01 |
| Peroxisomal lipid metabolism | 25 | 6.41e-01 | -5.39e-02 | 7.96e-01 |
| Signaling by VEGF | 89 | 3.81e-01 | 5.38e-02 | 6.05e-01 |
| Interleukin-7 signaling | 18 | 6.93e-01 | -5.38e-02 | 8.24e-01 |
| mTORC1-mediated signalling | 23 | 6.56e-01 | -5.37e-02 | 8.04e-01 |
| Keratan sulfate biosynthesis | 21 | 6.71e-01 | 5.37e-02 | 8.12e-01 |
| Platelet calcium homeostasis | 18 | 6.94e-01 | 5.36e-02 | 8.24e-01 |
| Cellular responses to stimuli | 639 | 2.22e-02 | -5.36e-02 | 1.04e-01 |
| B-WICH complex positively regulates rRNA expression | 38 | 5.68e-01 | -5.36e-02 | 7.49e-01 |
| Synthesis of IP3 and IP4 in the cytosol | 19 | 6.87e-01 | 5.35e-02 | 8.22e-01 |
| MyD88 cascade initiated on plasma membrane | 87 | 3.90e-01 | -5.34e-02 | 6.10e-01 |
| Toll Like Receptor 10 (TLR10) Cascade | 87 | 3.90e-01 | -5.34e-02 | 6.10e-01 |
| Toll Like Receptor 5 (TLR5) Cascade | 87 | 3.90e-01 | -5.34e-02 | 6.10e-01 |
| Cellular response to heat stress | 93 | 3.74e-01 | 5.34e-02 | 5.99e-01 |
| Diseases associated with O-glycosylation of proteins | 40 | 5.60e-01 | 5.33e-02 | 7.47e-01 |
| RA biosynthesis pathway | 12 | 7.49e-01 | 5.33e-02 | 8.53e-01 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 54 | 4.99e-01 | -5.32e-02 | 6.93e-01 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 54 | 4.99e-01 | -5.32e-02 | 6.93e-01 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 54 | 4.99e-01 | -5.32e-02 | 6.93e-01 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 54 | 4.99e-01 | -5.32e-02 | 6.93e-01 |
| Signaling by NOTCH1 in Cancer | 54 | 4.99e-01 | -5.32e-02 | 6.93e-01 |
| ZBP1(DAI) mediated induction of type I IFNs | 19 | 6.89e-01 | -5.30e-02 | 8.23e-01 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 16 | 7.14e-01 | 5.29e-02 | 8.37e-01 |
| Interleukin-17 signaling | 64 | 4.65e-01 | -5.28e-02 | 6.69e-01 |
| ABC-family proteins mediated transport | 87 | 3.96e-01 | -5.27e-02 | 6.12e-01 |
| The canonical retinoid cycle in rods (twilight vision) | 13 | 7.44e-01 | 5.22e-02 | 8.52e-01 |
| MTOR signalling | 39 | 5.77e-01 | -5.17e-02 | 7.56e-01 |
| Iron uptake and transport | 48 | 5.38e-01 | -5.14e-02 | 7.28e-01 |
| Transmission across Chemical Synapses | 141 | 2.94e-01 | 5.13e-02 | 5.20e-01 |
| Cell Cycle Checkpoints | 246 | 1.71e-01 | 5.09e-02 | 3.76e-01 |
| CTLA4 inhibitory signaling | 18 | 7.09e-01 | 5.08e-02 | 8.33e-01 |
| Signaling by Receptor Tyrosine Kinases | 392 | 8.88e-02 | 5.04e-02 | 2.56e-01 |
| Energy dependent regulation of mTOR by LKB1-AMPK | 28 | 6.45e-01 | -5.04e-02 | 7.98e-01 |
| Interleukin-1 family signaling | 125 | 3.33e-01 | -5.03e-02 | 5.49e-01 |
| Signalling to ERKs | 29 | 6.42e-01 | 4.99e-02 | 7.96e-01 |
| Signaling by ERBB4 | 45 | 5.65e-01 | -4.97e-02 | 7.48e-01 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 74 | 4.61e-01 | 4.96e-02 | 6.69e-01 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 94 | 4.07e-01 | 4.96e-02 | 6.22e-01 |
| HDACs deacetylate histones | 36 | 6.08e-01 | -4.94e-02 | 7.77e-01 |
| Cilium Assembly | 180 | 2.55e-01 | 4.93e-02 | 4.82e-01 |
| Interferon Signaling | 134 | 3.27e-01 | -4.92e-02 | 5.47e-01 |
| TNFs bind their physiological receptors | 14 | 7.52e-01 | 4.88e-02 | 8.55e-01 |
| Bile acid and bile salt metabolism | 24 | 6.79e-01 | -4.88e-02 | 8.17e-01 |
| TAK1-dependent IKK and NF-kappa-B activation | 38 | 6.04e-01 | -4.87e-02 | 7.75e-01 |
| Homology Directed Repair | 100 | 4.03e-01 | 4.85e-02 | 6.17e-01 |
| MAPK1/MAPK3 signaling | 219 | 2.23e-01 | 4.80e-02 | 4.39e-01 |
| Phospholipid metabolism | 162 | 2.99e-01 | 4.74e-02 | 5.25e-01 |
| Transcriptional regulation of white adipocyte differentiation | 71 | 4.91e-01 | -4.73e-02 | 6.92e-01 |
| PI3K/AKT Signaling in Cancer | 73 | 4.90e-01 | 4.68e-02 | 6.92e-01 |
| RHO GTPases activate KTN1 | 11 | 7.90e-01 | -4.63e-02 | 8.83e-01 |
| Negative regulation of MET activity | 19 | 7.28e-01 | -4.62e-02 | 8.42e-01 |
| Cytosolic sulfonation of small molecules | 17 | 7.43e-01 | -4.59e-02 | 8.52e-01 |
| Peptide hormone metabolism | 49 | 5.81e-01 | 4.56e-02 | 7.58e-01 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 29 | 6.72e-01 | 4.55e-02 | 8.12e-01 |
| Insulin receptor recycling | 20 | 7.26e-01 | 4.52e-02 | 8.42e-01 |
| Activation of GABAB receptors | 24 | 7.02e-01 | -4.52e-02 | 8.29e-01 |
| GABA B receptor activation | 24 | 7.02e-01 | -4.52e-02 | 8.29e-01 |
| Signaling by Nuclear Receptors | 194 | 2.81e-01 | 4.50e-02 | 5.06e-01 |
| Striated Muscle Contraction | 19 | 7.38e-01 | -4.44e-02 | 8.47e-01 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 16 | 7.60e-01 | 4.41e-02 | 8.62e-01 |
| Toll Like Receptor 9 (TLR9) Cascade | 96 | 4.57e-01 | -4.40e-02 | 6.68e-01 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 13 | 7.84e-01 | 4.38e-02 | 8.81e-01 |
| Pre-NOTCH Processing in Golgi | 14 | 7.77e-01 | 4.37e-02 | 8.77e-01 |
| SUMOylation of transcription cofactors | 42 | 6.25e-01 | -4.36e-02 | 7.84e-01 |
| Nervous system development | 432 | 1.25e-01 | -4.34e-02 | 3.17e-01 |
| Platelet sensitization by LDL | 15 | 7.75e-01 | 4.26e-02 | 8.76e-01 |
| RUNX2 regulates osteoblast differentiation | 21 | 7.36e-01 | -4.26e-02 | 8.46e-01 |
| Surfactant metabolism | 13 | 7.92e-01 | -4.22e-02 | 8.83e-01 |
| Mitotic G1 phase and G1/S transition | 143 | 3.86e-01 | -4.21e-02 | 6.08e-01 |
| Signaling by Hedgehog | 116 | 4.35e-01 | 4.20e-02 | 6.49e-01 |
| HCMV Infection | 84 | 5.09e-01 | 4.17e-02 | 7.02e-01 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | 15 | 7.80e-01 | 4.17e-02 | 8.78e-01 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 36 | 6.66e-01 | -4.16e-02 | 8.09e-01 |
| ESR-mediated signaling | 143 | 3.95e-01 | 4.13e-02 | 6.11e-01 |
| Early Phase of HIV Life Cycle | 10 | 8.21e-01 | 4.12e-02 | 9.00e-01 |
| SUMOylation of chromatin organization proteins | 53 | 6.05e-01 | 4.11e-02 | 7.76e-01 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 49 | 6.23e-01 | 4.07e-02 | 7.83e-01 |
| TP53 Regulates Transcription of Cell Cycle Genes | 46 | 6.33e-01 | 4.07e-02 | 7.89e-01 |
| Glycogen metabolism | 22 | 7.42e-01 | -4.05e-02 | 8.52e-01 |
| G2/M Checkpoints | 131 | 4.29e-01 | -4.02e-02 | 6.41e-01 |
| CD28 co-stimulation | 28 | 7.15e-01 | 3.99e-02 | 8.38e-01 |
| HATs acetylate histones | 82 | 5.35e-01 | 3.97e-02 | 7.27e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 13 | 8.04e-01 | 3.97e-02 | 8.92e-01 |
| Viral Messenger RNA Synthesis | 43 | 6.59e-01 | -3.89e-02 | 8.04e-01 |
| DNA Repair | 282 | 2.67e-01 | -3.86e-02 | 4.90e-01 |
| Class B/2 (Secretin family receptors) | 36 | 6.91e-01 | -3.83e-02 | 8.23e-01 |
| Cell Cycle | 594 | 1.15e-01 | 3.83e-02 | 3.00e-01 |
| Beta-catenin independent WNT signaling | 129 | 4.54e-01 | -3.83e-02 | 6.67e-01 |
| Signaling by ERBB2 TMD/JMD mutants | 20 | 7.70e-01 | -3.78e-02 | 8.70e-01 |
| Generation of second messenger molecules | 12 | 8.22e-01 | -3.75e-02 | 9.00e-01 |
| HCMV Late Events | 58 | 6.22e-01 | 3.74e-02 | 7.83e-01 |
| O-glycosylation of TSR domain-containing proteins | 25 | 7.46e-01 | 3.74e-02 | 8.53e-01 |
| Mismatch Repair | 14 | 8.10e-01 | 3.72e-02 | 8.94e-01 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 14 | 8.10e-01 | 3.71e-02 | 8.94e-01 |
| Intrinsic Pathway for Apoptosis | 48 | 6.59e-01 | -3.69e-02 | 8.04e-01 |
| Immune System | 1317 | 2.94e-02 | 3.67e-02 | 1.26e-01 |
| Class A/1 (Rhodopsin-like receptors) | 79 | 5.76e-01 | 3.64e-02 | 7.56e-01 |
| Nuclear events stimulated by ALK signaling in cancer | 17 | 7.95e-01 | 3.64e-02 | 8.84e-01 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 20 | 7.80e-01 | -3.62e-02 | 8.78e-01 |
| Apoptotic factor-mediated response | 17 | 7.97e-01 | -3.61e-02 | 8.85e-01 |
| Transcriptional activation of mitochondrial biogenesis | 51 | 6.57e-01 | -3.60e-02 | 8.04e-01 |
| Incretin synthesis, secretion, and inactivation | 10 | 8.44e-01 | -3.59e-02 | 9.12e-01 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 10 | 8.44e-01 | -3.59e-02 | 9.12e-01 |
| Transcriptional regulation by small RNAs | 53 | 6.53e-01 | 3.57e-02 | 8.04e-01 |
| Metabolism of cofactors | 16 | 8.09e-01 | -3.49e-02 | 8.94e-01 |
| Response of Mtb to phagocytosis | 20 | 7.88e-01 | 3.48e-02 | 8.83e-01 |
| Antigen processing: Ubiquitination & Proteasome degradation | 269 | 3.30e-01 | -3.46e-02 | 5.48e-01 |
| Signaling by Non-Receptor Tyrosine Kinases | 51 | 6.72e-01 | -3.43e-02 | 8.12e-01 |
| Signaling by PTK6 | 51 | 6.72e-01 | -3.43e-02 | 8.12e-01 |
| Nicotinamide salvaging | 16 | 8.13e-01 | 3.41e-02 | 8.96e-01 |
| Signaling by SCF-KIT | 33 | 7.35e-01 | 3.40e-02 | 8.46e-01 |
| COPI-independent Golgi-to-ER retrograde traffic | 30 | 7.47e-01 | 3.40e-02 | 8.53e-01 |
| Smooth Muscle Contraction | 33 | 7.36e-01 | 3.39e-02 | 8.46e-01 |
| Association of TriC/CCT with target proteins during biosynthesis | 37 | 7.22e-01 | 3.38e-02 | 8.42e-01 |
| Platelet homeostasis | 55 | 6.65e-01 | -3.37e-02 | 8.09e-01 |
| Regulation of localization of FOXO transcription factors | 11 | 8.47e-01 | 3.36e-02 | 9.12e-01 |
| GAB1 signalosome | 14 | 8.31e-01 | -3.30e-02 | 9.03e-01 |
| Regulation of TP53 Activity | 148 | 4.90e-01 | -3.29e-02 | 6.92e-01 |
| PIP3 activates AKT signaling | 231 | 3.94e-01 | -3.27e-02 | 6.11e-01 |
| Disease | 1313 | 5.27e-02 | 3.27e-02 | 1.82e-01 |
| Infectious disease | 707 | 1.44e-01 | -3.27e-02 | 3.44e-01 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 13 | 8.39e-01 | -3.25e-02 | 9.09e-01 |
| Signaling by EGFR | 46 | 7.04e-01 | 3.24e-02 | 8.29e-01 |
| RAF/MAP kinase cascade | 214 | 4.16e-01 | 3.24e-02 | 6.32e-01 |
| Visual phototransduction | 57 | 6.73e-01 | 3.24e-02 | 8.12e-01 |
| Potential therapeutics for SARS | 79 | 6.23e-01 | -3.21e-02 | 7.83e-01 |
| Cargo trafficking to the periciliary membrane | 48 | 7.01e-01 | 3.21e-02 | 8.29e-01 |
| G-protein beta:gamma signalling | 22 | 7.95e-01 | -3.20e-02 | 8.84e-01 |
| SUMOylation of DNA damage response and repair proteins | 73 | 6.37e-01 | 3.19e-02 | 7.93e-01 |
| Signaling by ERBB2 ECD mutants | 16 | 8.26e-01 | 3.18e-02 | 9.01e-01 |
| Ub-specific processing proteases | 158 | 4.94e-01 | 3.16e-02 | 6.93e-01 |
| Interleukin-15 signaling | 12 | 8.50e-01 | 3.16e-02 | 9.12e-01 |
| Caspase activation via extrinsic apoptotic signalling pathway | 20 | 8.11e-01 | 3.09e-02 | 8.94e-01 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 12 | 8.53e-01 | -3.09e-02 | 9.13e-01 |
| Activated NOTCH1 Transmits Signal to the Nucleus | 27 | 7.82e-01 | -3.08e-02 | 8.79e-01 |
| Metabolism of nucleotides | 81 | 6.33e-01 | 3.07e-02 | 7.89e-01 |
| Fanconi Anemia Pathway | 35 | 7.53e-01 | -3.07e-02 | 8.56e-01 |
| Drug ADME | 41 | 7.36e-01 | 3.04e-02 | 8.46e-01 |
| Trafficking of GluR2-containing AMPA receptors | 13 | 8.50e-01 | -3.04e-02 | 9.12e-01 |
| Diseases of DNA repair | 51 | 7.09e-01 | 3.02e-02 | 8.33e-01 |
| rRNA modification in the nucleus and cytosol | 59 | 6.90e-01 | -3.01e-02 | 8.23e-01 |
| Signaling by NOTCH1 | 68 | 6.73e-01 | -2.97e-02 | 8.12e-01 |
| Programmed Cell Death | 174 | 5.03e-01 | -2.95e-02 | 6.96e-01 |
| Signaling by ERBB2 | 47 | 7.27e-01 | -2.95e-02 | 8.42e-01 |
| G2/M DNA damage checkpoint | 61 | 6.91e-01 | 2.94e-02 | 8.23e-01 |
| Activation of BAD and translocation to mitochondria | 15 | 8.46e-01 | 2.89e-02 | 9.12e-01 |
| Amino acids regulate mTORC1 | 48 | 7.30e-01 | 2.89e-02 | 8.43e-01 |
| BBSome-mediated cargo-targeting to cilium | 22 | 8.15e-01 | -2.88e-02 | 8.97e-01 |
| Transport of vitamins, nucleosides, and related molecules | 24 | 8.08e-01 | 2.87e-02 | 8.94e-01 |
| Diseases associated with the TLR signaling cascade | 21 | 8.21e-01 | -2.86e-02 | 9.00e-01 |
| Diseases of Immune System | 21 | 8.21e-01 | -2.86e-02 | 9.00e-01 |
| SARS-CoV-2-host interactions | 156 | 5.42e-01 | -2.84e-02 | 7.32e-01 |
| Post-chaperonin tubulin folding pathway | 16 | 8.45e-01 | -2.83e-02 | 9.12e-01 |
| Signaling by NOTCH | 166 | 5.34e-01 | -2.81e-02 | 7.27e-01 |
| FLT3 Signaling | 32 | 7.85e-01 | 2.79e-02 | 8.81e-01 |
| Infection with Mycobacterium tuberculosis | 22 | 8.21e-01 | -2.78e-02 | 9.00e-01 |
| TNFR1-induced proapoptotic signaling | 12 | 8.70e-01 | -2.74e-02 | 9.24e-01 |
| Uptake and actions of bacterial toxins | 22 | 8.25e-01 | 2.72e-02 | 9.01e-01 |
| Biological oxidations | 116 | 6.20e-01 | -2.67e-02 | 7.83e-01 |
| RUNX3 regulates NOTCH signaling | 14 | 8.63e-01 | 2.66e-02 | 9.19e-01 |
| Diseases associated with N-glycosylation of proteins | 20 | 8.40e-01 | -2.62e-02 | 9.09e-01 |
| SARS-CoV-2 Infection | 235 | 4.92e-01 | 2.61e-02 | 6.92e-01 |
| MAPK family signaling cascades | 256 | 4.76e-01 | 2.60e-02 | 6.81e-01 |
| Costimulation by the CD28 family | 44 | 7.66e-01 | 2.60e-02 | 8.67e-01 |
| Estrogen-dependent gene expression | 88 | 6.77e-01 | 2.57e-02 | 8.14e-01 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 17 | 8.55e-01 | 2.56e-02 | 9.13e-01 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 17 | 8.55e-01 | 2.56e-02 | 9.13e-01 |
| G alpha (i) signalling events | 124 | 6.24e-01 | -2.55e-02 | 7.84e-01 |
| Innate Immune System | 692 | 2.61e-01 | 2.54e-02 | 4.87e-01 |
| Neuronal System | 201 | 5.38e-01 | 2.53e-02 | 7.28e-01 |
| Cell junction organization | 55 | 7.50e-01 | 2.49e-02 | 8.53e-01 |
| Signaling by ALK | 21 | 8.44e-01 | 2.49e-02 | 9.12e-01 |
| Other interleukin signaling | 14 | 8.72e-01 | -2.48e-02 | 9.27e-01 |
| Constitutive Signaling by AKT1 E17K in Cancer | 25 | 8.32e-01 | -2.46e-02 | 9.03e-01 |
| TRAF6 mediated NF-kB activation | 19 | 8.54e-01 | 2.44e-02 | 9.13e-01 |
| Recognition of DNA damage by PCNA-containing replication complex | 29 | 8.21e-01 | -2.43e-02 | 9.00e-01 |
| Downregulation of TGF-beta receptor signaling | 26 | 8.31e-01 | -2.42e-02 | 9.03e-01 |
| Stimuli-sensing channels | 53 | 7.61e-01 | -2.42e-02 | 8.63e-01 |
| Carboxyterminal post-translational modifications of tubulin | 28 | 8.28e-01 | 2.37e-02 | 9.02e-01 |
| HDR through Single Strand Annealing (SSA) | 37 | 8.04e-01 | 2.36e-02 | 8.92e-01 |
| Adherens junctions interactions | 19 | 8.59e-01 | 2.35e-02 | 9.15e-01 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 14 | 8.80e-01 | 2.32e-02 | 9.31e-01 |
| SUMOylation of RNA binding proteins | 45 | 7.90e-01 | -2.30e-02 | 8.83e-01 |
| Prefoldin mediated transfer of substrate to CCT/TriC | 24 | 8.47e-01 | -2.28e-02 | 9.12e-01 |
| Opioid Signalling | 66 | 7.50e-01 | 2.27e-02 | 8.53e-01 |
| Signaling by ERBB2 in Cancer | 24 | 8.49e-01 | 2.25e-02 | 9.12e-01 |
| E3 ubiquitin ligases ubiquitinate target proteins | 43 | 8.05e-01 | -2.17e-02 | 8.92e-01 |
| Defective Intrinsic Pathway for Apoptosis | 23 | 8.57e-01 | -2.17e-02 | 9.14e-01 |
| Regulated proteolysis of p75NTR | 10 | 9.06e-01 | 2.16e-02 | 9.51e-01 |
| Pyrimidine salvage | 10 | 9.09e-01 | -2.09e-02 | 9.51e-01 |
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 11 | 9.06e-01 | 2.05e-02 | 9.51e-01 |
| TNF signaling | 43 | 8.27e-01 | -1.92e-02 | 9.02e-01 |
| Sialic acid metabolism | 23 | 8.73e-01 | -1.92e-02 | 9.27e-01 |
| HSF1-dependent transactivation | 31 | 8.55e-01 | -1.90e-02 | 9.13e-01 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 44 | 8.28e-01 | 1.89e-02 | 9.02e-01 |
| Amyloid fiber formation | 42 | 8.34e-01 | -1.87e-02 | 9.05e-01 |
| Organelle biogenesis and maintenance | 268 | 6.10e-01 | -1.82e-02 | 7.79e-01 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 49 | 8.26e-01 | 1.81e-02 | 9.01e-01 |
| DNA Double-Strand Break Repair | 130 | 7.31e-01 | 1.75e-02 | 8.44e-01 |
| Toll-like Receptor Cascades | 134 | 7.28e-01 | -1.74e-02 | 8.42e-01 |
| Defective B3GALTL causes PpS | 24 | 8.83e-01 | 1.74e-02 | 9.31e-01 |
| Intraflagellar transport | 37 | 8.58e-01 | 1.71e-02 | 9.14e-01 |
| RAB GEFs exchange GTP for GDP on RABs | 84 | 7.89e-01 | -1.69e-02 | 8.83e-01 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | 34 | 8.66e-01 | -1.68e-02 | 9.21e-01 |
| Ion channel transport | 98 | 7.82e-01 | 1.62e-02 | 8.79e-01 |
| G alpha (q) signalling events | 95 | 7.92e-01 | -1.57e-02 | 8.83e-01 |
| Oncogene Induced Senescence | 32 | 8.79e-01 | 1.55e-02 | 9.31e-01 |
| G2/M Transition | 177 | 7.24e-01 | -1.54e-02 | 8.42e-01 |
| RHOBTB GTPase Cycle | 35 | 8.75e-01 | 1.54e-02 | 9.28e-01 |
| SHC1 events in ERBB4 signaling | 12 | 9.27e-01 | -1.53e-02 | 9.59e-01 |
| RAS processing | 19 | 9.09e-01 | 1.52e-02 | 9.51e-01 |
| Glutamate and glutamine metabolism | 11 | 9.31e-01 | -1.51e-02 | 9.60e-01 |
| tRNA processing in the nucleus | 56 | 8.49e-01 | 1.48e-02 | 9.12e-01 |
| Nuclear Events (kinase and transcription factor activation) | 55 | 8.51e-01 | 1.46e-02 | 9.12e-01 |
| Signaling by WNT | 240 | 6.98e-01 | -1.46e-02 | 8.28e-01 |
| Hedgehog ‘off’ state | 89 | 8.12e-01 | -1.46e-02 | 8.95e-01 |
| Cardiac conduction | 57 | 8.51e-01 | -1.44e-02 | 9.12e-01 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models | 21 | 9.10e-01 | 1.43e-02 | 9.51e-01 |
| Neurodegenerative Diseases | 21 | 9.10e-01 | 1.43e-02 | 9.51e-01 |
| Diseases of carbohydrate metabolism | 29 | 8.95e-01 | -1.42e-02 | 9.42e-01 |
| Metabolism of steroid hormones | 18 | 9.21e-01 | -1.35e-02 | 9.59e-01 |
| Transcription of E2F targets under negative control by DREAM complex | 19 | 9.19e-01 | 1.34e-02 | 9.59e-01 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 16 | 9.27e-01 | 1.33e-02 | 9.59e-01 |
| Disorders of transmembrane transporters | 132 | 7.95e-01 | 1.31e-02 | 8.84e-01 |
| TCF dependent signaling in response to WNT | 160 | 7.77e-01 | 1.30e-02 | 8.77e-01 |
| Uptake and function of anthrax toxins | 10 | 9.44e-01 | 1.28e-02 | 9.66e-01 |
| Apoptosis | 153 | 7.87e-01 | -1.27e-02 | 8.82e-01 |
| Post-translational modification: synthesis of GPI-anchored proteins | 48 | 8.81e-01 | -1.25e-02 | 9.31e-01 |
| Class I peroxisomal membrane protein import | 18 | 9.27e-01 | 1.25e-02 | 9.59e-01 |
| Caspase-mediated cleavage of cytoskeletal proteins | 12 | 9.41e-01 | -1.22e-02 | 9.65e-01 |
| GPCR ligand binding | 117 | 8.20e-01 | 1.22e-02 | 9.00e-01 |
| Unblocking of NMDA receptors, glutamate binding and activation | 14 | 9.39e-01 | 1.18e-02 | 9.65e-01 |
| Metabolism of non-coding RNA | 52 | 8.83e-01 | -1.18e-02 | 9.31e-01 |
| snRNP Assembly | 52 | 8.83e-01 | -1.18e-02 | 9.31e-01 |
| Signaling by FGFR in disease | 52 | 8.86e-01 | 1.15e-02 | 9.34e-01 |
| SARS-CoV-2 modulates autophagy | 10 | 9.50e-01 | -1.14e-02 | 9.70e-01 |
| Binding and Uptake of Ligands by Scavenger Receptors | 26 | 9.22e-01 | 1.10e-02 | 9.59e-01 |
| Cytochrome P450 - arranged by substrate type | 27 | 9.22e-01 | 1.09e-02 | 9.59e-01 |
| Vasopressin regulates renal water homeostasis via Aquaporins | 27 | 9.23e-01 | -1.08e-02 | 9.59e-01 |
| Signaling by Retinoic Acid | 30 | 9.20e-01 | 1.06e-02 | 9.59e-01 |
| Signaling by Interleukins | 329 | 7.49e-01 | 1.03e-02 | 8.53e-01 |
| DCC mediated attractive signaling | 12 | 9.53e-01 | -9.81e-03 | 9.70e-01 |
| Deposition of new CENPA-containing nucleosomes at the centromere | 32 | 9.24e-01 | 9.78e-03 | 9.59e-01 |
| Nucleosome assembly | 32 | 9.24e-01 | 9.78e-03 | 9.59e-01 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 19 | 9.42e-01 | 9.68e-03 | 9.65e-01 |
| Processing of DNA double-strand break ends | 61 | 8.97e-01 | 9.59e-03 | 9.43e-01 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 30 | 9.28e-01 | 9.48e-03 | 9.59e-01 |
| Attenuation phase | 22 | 9.41e-01 | 9.10e-03 | 9.65e-01 |
| Nuclear Receptor transcription pathway | 34 | 9.28e-01 | -8.99e-03 | 9.59e-01 |
| VLDLR internalisation and degradation | 15 | 9.53e-01 | 8.88e-03 | 9.70e-01 |
| Citric acid cycle (TCA cycle) | 22 | 9.43e-01 | 8.85e-03 | 9.65e-01 |
| Cargo recognition for clathrin-mediated endocytosis | 83 | 8.89e-01 | -8.85e-03 | 9.37e-01 |
| SARS-CoV Infections | 305 | 7.92e-01 | 8.82e-03 | 8.83e-01 |
| TP53 Regulates Transcription of Cell Death Genes | 34 | 9.31e-01 | 8.64e-03 | 9.60e-01 |
| Activation of BH3-only proteins | 27 | 9.40e-01 | 8.35e-03 | 9.65e-01 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 37 | 9.30e-01 | 8.33e-03 | 9.60e-01 |
| Peptide ligand-binding receptors | 42 | 9.27e-01 | 8.15e-03 | 9.59e-01 |
| IL-6-type cytokine receptor ligand interactions | 14 | 9.58e-01 | 8.12e-03 | 9.72e-01 |
| Regulation of NF-kappa B signaling | 17 | 9.54e-01 | -8.10e-03 | 9.70e-01 |
| Signaling by Activin | 13 | 9.60e-01 | 8.03e-03 | 9.74e-01 |
| EPH-Ephrin signaling | 80 | 9.01e-01 | 8.03e-03 | 9.47e-01 |
| Lagging Strand Synthesis | 19 | 9.53e-01 | 7.82e-03 | 9.70e-01 |
| Adaptive Immune System | 533 | 7.65e-01 | 7.64e-03 | 8.66e-01 |
| Signaling by NOTCH2 | 28 | 9.46e-01 | -7.40e-03 | 9.66e-01 |
| Aquaporin-mediated transport | 30 | 9.44e-01 | -7.38e-03 | 9.66e-01 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 57 | 9.27e-01 | -6.98e-03 | 9.59e-01 |
| Signaling by FGFR1 | 41 | 9.39e-01 | 6.93e-03 | 9.65e-01 |
| Mitotic G2-G2/M phases | 179 | 8.80e-01 | -6.56e-03 | 9.31e-01 |
| Netrin-1 signaling | 36 | 9.49e-01 | -6.13e-03 | 9.69e-01 |
| Cytokine Signaling in Immune system | 492 | 8.26e-01 | -5.85e-03 | 9.01e-01 |
| Listeria monocytogenes entry into host cells | 18 | 9.70e-01 | 5.09e-03 | 9.82e-01 |
| Metabolism of proteins | 1508 | 7.49e-01 | -5.08e-03 | 8.53e-01 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 16 | 9.73e-01 | -4.93e-03 | 9.84e-01 |
| FOXO-mediated transcription | 54 | 9.54e-01 | -4.50e-03 | 9.70e-01 |
| Metabolism | 1593 | 7.95e-01 | -4.04e-03 | 8.84e-01 |
| Fatty acid metabolism | 128 | 9.41e-01 | -3.79e-03 | 9.65e-01 |
| Regulation of TNFR1 signaling | 34 | 9.70e-01 | 3.69e-03 | 9.82e-01 |
| Class I MHC mediated antigen processing & presentation | 315 | 9.13e-01 | -3.60e-03 | 9.54e-01 |
| KSRP (KHSRP) binds and destabilizes mRNA | 16 | 9.81e-01 | 3.48e-03 | 9.89e-01 |
| Muscle contraction | 104 | 9.55e-01 | 3.18e-03 | 9.70e-01 |
| Intracellular signaling by second messengers | 262 | 9.35e-01 | -2.93e-03 | 9.63e-01 |
| Regulation of IFNA/IFNB signaling | 11 | 9.87e-01 | -2.87e-03 | 9.92e-01 |
| Protein ubiquitination | 63 | 9.69e-01 | 2.83e-03 | 9.82e-01 |
| Gap junction trafficking | 13 | 9.86e-01 | -2.79e-03 | 9.92e-01 |
| Diseases of programmed cell death | 48 | 9.78e-01 | 2.35e-03 | 9.88e-01 |
| Signaling by ERBB2 KD Mutants | 23 | 9.85e-01 | 2.26e-03 | 9.92e-01 |
| DNA Damage/Telomere Stress Induced Senescence | 37 | 9.84e-01 | -1.90e-03 | 9.92e-01 |
| Regulation of TP53 Activity through Phosphorylation | 89 | 9.79e-01 | 1.60e-03 | 9.89e-01 |
| SARS-CoV-1 Infection | 45 | 9.85e-01 | 1.59e-03 | 9.92e-01 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 25 | 9.91e-01 | 1.30e-03 | 9.95e-01 |
| Processing of Intronless Pre-mRNAs | 19 | 9.94e-01 | 1.01e-03 | 9.98e-01 |
| RIP-mediated NFkB activation via ZBP1 | 16 | 9.95e-01 | 9.47e-04 | 9.98e-01 |
| Voltage gated Potassium channels | 11 | 9.97e-01 | 7.63e-04 | 9.98e-01 |
| Mitochondrial calcium ion transport | 20 | 9.97e-01 | -5.05e-04 | 9.98e-01 |
| Deadenylation of mRNA | 21 | 9.97e-01 | -4.93e-04 | 9.98e-01 |
| Nicotinate metabolism | 25 | 1.00e+00 | -3.59e-05 | 1.00e+00 |
tRNA processing in the mitochondrion
| 1366 | |
|---|---|
| set | tRNA processing in the mitochondrion |
| setSize | 18 |
| pANOVA | 2.56e-07 |
| s.dist | -0.701 |
| p.adjustANOVA | 8.76e-06 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MT-ND6 | -6005 |
| MT-ND2 | -5987 |
| MT-ND4 | -5978 |
| MT-ND1 | -5971 |
| MT-CYB | -5962 |
| MT-ATP8 | -5958 |
| MT-ATP6 | -5894 |
| MT-CO1 | -5824 |
| MT-CO3 | -5645 |
| HSD17B10 | -5546 |
| MT-ND5 | -5464 |
| MT-ND3 | -4901 |
| ELAC2 | -2846 |
| MT-ND4L | -2630 |
| PRORP | -1452 |
| TRMT10C | -1393 |
| TRNT1 | -1379 |
| MT-CO2 | 3727 |
| GeneID | Gene Rank |
|---|---|
| MT-ND6 | -6005 |
| MT-ND2 | -5987 |
| MT-ND4 | -5978 |
| MT-ND1 | -5971 |
| MT-CYB | -5962 |
| MT-ATP8 | -5958 |
| MT-ATP6 | -5894 |
| MT-CO1 | -5824 |
| MT-CO3 | -5645 |
| HSD17B10 | -5546 |
| MT-ND5 | -5464 |
| MT-ND3 | -4901 |
| ELAC2 | -2846 |
| MT-ND4L | -2630 |
| PRORP | -1452 |
| TRMT10C | -1393 |
| TRNT1 | -1379 |
| MT-CO2 | 3727 |
Cholesterol biosynthesis
| 168 | |
|---|---|
| set | Cholesterol biosynthesis |
| setSize | 26 |
| pANOVA | 1.02e-09 |
| s.dist | 0.692 |
| p.adjustANOVA | 4.97e-08 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HMGCR | 6265 |
| LSS | 6244 |
| SQLE | 6233 |
| DHCR24 | 6229 |
| HMGCS1 | 6164 |
| CYP51A1 | 6076 |
| IDI1 | 6007 |
| NSDHL | 5988 |
| LBR | 5976 |
| FDPS | 5929 |
| SC5D | 5919 |
| MVD | 5889 |
| SREBF2 | 5879 |
| HSD17B7 | 5862 |
| ACAT2 | 5688 |
| MSMO1 | 5648 |
| FDFT1 | 4557 |
| MVK | 4426 |
| TM7SF2 | 3914 |
| PMVK | 3782 |
| GeneID | Gene Rank |
|---|---|
| HMGCR | 6265 |
| LSS | 6244 |
| SQLE | 6233 |
| DHCR24 | 6229 |
| HMGCS1 | 6164 |
| CYP51A1 | 6076 |
| IDI1 | 6007 |
| NSDHL | 5988 |
| LBR | 5976 |
| FDPS | 5929 |
| SC5D | 5919 |
| MVD | 5889 |
| SREBF2 | 5879 |
| HSD17B7 | 5862 |
| ACAT2 | 5688 |
| MSMO1 | 5648 |
| FDFT1 | 4557 |
| MVK | 4426 |
| TM7SF2 | 3914 |
| PMVK | 3782 |
| DHCR7 | 3729 |
| SREBF1 | 3235 |
| EBP | -347 |
| ARV1 | -823 |
| GGPS1 | -2279 |
| PLPP6 | -2486 |
rRNA processing in the mitochondrion
| 1360 | |
|---|---|
| set | rRNA processing in the mitochondrion |
| setSize | 21 |
| pANOVA | 8.74e-07 |
| s.dist | -0.62 |
| p.adjustANOVA | 2.54e-05 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MTERF4 | -5997 |
| MT-ND2 | -5987 |
| MT-ND4 | -5978 |
| MT-ND1 | -5971 |
| MT-CYB | -5962 |
| MT-ATP8 | -5958 |
| MT-ATP6 | -5894 |
| MT-CO1 | -5824 |
| MT-CO3 | -5645 |
| HSD17B10 | -5546 |
| MT-ND5 | -5464 |
| MT-ND3 | -4901 |
| ELAC2 | -2846 |
| MT-ND4L | -2630 |
| MRM2 | -2026 |
| TFB1M | -1577 |
| PRORP | -1452 |
| TRMT10C | -1393 |
| MRM1 | -41 |
| MRM3 | 266 |
| GeneID | Gene Rank |
|---|---|
| MTERF4 | -5997 |
| MT-ND2 | -5987 |
| MT-ND4 | -5978 |
| MT-ND1 | -5971 |
| MT-CYB | -5962 |
| MT-ATP8 | -5958 |
| MT-ATP6 | -5894 |
| MT-CO1 | -5824 |
| MT-CO3 | -5645 |
| HSD17B10 | -5546 |
| MT-ND5 | -5464 |
| MT-ND3 | -4901 |
| ELAC2 | -2846 |
| MT-ND4L | -2630 |
| MRM2 | -2026 |
| TFB1M | -1577 |
| PRORP | -1452 |
| TRMT10C | -1393 |
| MRM1 | -41 |
| MRM3 | 266 |
| MT-CO2 | 3727 |
MET activates PTK2 signaling
| 611 | |
|---|---|
| set | MET activates PTK2 signaling |
| setSize | 12 |
| pANOVA | 0.000611 |
| s.dist | 0.571 |
| p.adjustANOVA | 0.00812 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ITGB1 | 6188 |
| LAMA5 | 5762 |
| LAMB2 | 4913 |
| ITGA2 | 4663 |
| PTK2 | 4333 |
| ITGA3 | 4068 |
| LAMC1 | 4028 |
| LAMC2 | 3528 |
| LAMB1 | 3200 |
| LAMB3 | 3026 |
| SRC | 571 |
| MET | -615 |
| GeneID | Gene Rank |
|---|---|
| ITGB1 | 6188 |
| LAMA5 | 5762 |
| LAMB2 | 4913 |
| ITGA2 | 4663 |
| PTK2 | 4333 |
| ITGA3 | 4068 |
| LAMC1 | 4028 |
| LAMC2 | 3528 |
| LAMB1 | 3200 |
| LAMB3 | 3026 |
| SRC | 571 |
| MET | -615 |
ALK mutants bind TKIs
| 9 | |
|---|---|
| set | ALK mutants bind TKIs |
| setSize | 10 |
| pANOVA | 0.0021 |
| s.dist | 0.562 |
| p.adjustANOVA | 0.0207 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| BIRC6 | 6182 |
| CLTC | 6133 |
| FN1 | 6049 |
| PPM1B | 4960 |
| PRKAR1A | 4931 |
| STRN | 4727 |
| EIF2AK3 | 4721 |
| HIP1 | 4546 |
| EML4 | -1728 |
| NPM1 | -4720 |
| GeneID | Gene Rank |
|---|---|
| BIRC6 | 6182 |
| CLTC | 6133 |
| FN1 | 6049 |
| PPM1B | 4960 |
| PRKAR1A | 4931 |
| STRN | 4727 |
| EIF2AK3 | 4721 |
| HIP1 | 4546 |
| EML4 | -1728 |
| NPM1 | -4720 |
Laminin interactions
| 587 | |
|---|---|
| set | Laminin interactions |
| setSize | 18 |
| pANOVA | 3.71e-05 |
| s.dist | 0.562 |
| p.adjustANOVA | 0.000715 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ITGAV | 6242 |
| ITGB1 | 6188 |
| HSPG2 | 5946 |
| LAMA5 | 5762 |
| ITGA7 | 5646 |
| LAMB2 | 4913 |
| ITGA2 | 4663 |
| ITGA3 | 4068 |
| LAMC1 | 4028 |
| NID1 | 3709 |
| COL18A1 | 3647 |
| ITGA1 | 3532 |
| LAMC2 | 3528 |
| LAMB1 | 3200 |
| LAMB3 | 3026 |
| ITGB4 | 1902 |
| ITGA6 | 312 |
| NID2 | -5917 |
| GeneID | Gene Rank |
|---|---|
| ITGAV | 6242 |
| ITGB1 | 6188 |
| HSPG2 | 5946 |
| LAMA5 | 5762 |
| ITGA7 | 5646 |
| LAMB2 | 4913 |
| ITGA2 | 4663 |
| ITGA3 | 4068 |
| LAMC1 | 4028 |
| NID1 | 3709 |
| COL18A1 | 3647 |
| ITGA1 | 3532 |
| LAMC2 | 3528 |
| LAMB1 | 3200 |
| LAMB3 | 3026 |
| ITGB4 | 1902 |
| ITGA6 | 312 |
| NID2 | -5917 |
Apoptosis induced DNA fragmentation
| 70 | |
|---|---|
| set | Apoptosis induced DNA fragmentation |
| setSize | 10 |
| pANOVA | 0.00504 |
| s.dist | 0.512 |
| p.adjustANOVA | 0.0356 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| H1-2 | 6223 |
| KPNB1 | 5121 |
| HMGB2 | 4819 |
| H1-3 | 4523 |
| H1-4 | 4202 |
| H1-0 | 3395 |
| DFFA | 2346 |
| KPNA1 | 1250 |
| CASP3 | 592 |
| DFFB | 292 |
| GeneID | Gene Rank |
|---|---|
| H1-2 | 6223 |
| KPNB1 | 5121 |
| HMGB2 | 4819 |
| H1-3 | 4523 |
| H1-4 | 4202 |
| H1-0 | 3395 |
| DFFA | 2346 |
| KPNA1 | 1250 |
| CASP3 | 592 |
| DFFB | 292 |
Membrane binding and targetting of GAG proteins
| 623 | |
|---|---|
| set | Membrane binding and targetting of GAG proteins |
| setSize | 14 |
| pANOVA | 0.0012 |
| s.dist | -0.5 |
| p.adjustANOVA | 0.0143 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UBA52 | -5753 |
| TSG101 | -5714 |
| VPS28 | -5424 |
| RPS27A | -5344 |
| UBAP1 | -5098 |
| UBB | -4930 |
| MVB12A | -4676 |
| NMT2 | -3113 |
| VPS37B | -2145 |
| MVB12B | -2090 |
| VPS37D | -2032 |
| VPS37C | -607 |
| UBC | 1127 |
| VPS37A | 4688 |
| GeneID | Gene Rank |
|---|---|
| UBA52 | -5753 |
| TSG101 | -5714 |
| VPS28 | -5424 |
| RPS27A | -5344 |
| UBAP1 | -5098 |
| UBB | -4930 |
| MVB12A | -4676 |
| NMT2 | -3113 |
| VPS37B | -2145 |
| MVB12B | -2090 |
| VPS37D | -2032 |
| VPS37C | -607 |
| UBC | 1127 |
| VPS37A | 4688 |
Synthesis And Processing Of GAG, GAGPOL Polyproteins
| 1182 | |
|---|---|
| set | Synthesis And Processing Of GAG, GAGPOL Polyproteins |
| setSize | 14 |
| pANOVA | 0.0012 |
| s.dist | -0.5 |
| p.adjustANOVA | 0.0143 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UBA52 | -5753 |
| TSG101 | -5714 |
| VPS28 | -5424 |
| RPS27A | -5344 |
| UBAP1 | -5098 |
| UBB | -4930 |
| MVB12A | -4676 |
| NMT2 | -3113 |
| VPS37B | -2145 |
| MVB12B | -2090 |
| VPS37D | -2032 |
| VPS37C | -607 |
| UBC | 1127 |
| VPS37A | 4688 |
| GeneID | Gene Rank |
|---|---|
| UBA52 | -5753 |
| TSG101 | -5714 |
| VPS28 | -5424 |
| RPS27A | -5344 |
| UBAP1 | -5098 |
| UBB | -4930 |
| MVB12A | -4676 |
| NMT2 | -3113 |
| VPS37B | -2145 |
| MVB12B | -2090 |
| VPS37D | -2032 |
| VPS37C | -607 |
| UBC | 1127 |
| VPS37A | 4688 |
Formation of a pool of free 40S subunits
| 385 | |
|---|---|
| set | Formation of a pool of free 40S subunits |
| setSize | 79 |
| pANOVA | 4.97e-14 |
| s.dist | -0.49 |
| p.adjustANOVA | 1.72e-11 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| RPL29 | -5888 |
| EIF3F | -5822 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| EIF3K | -5794 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| RPS27A | -5344 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| RPL29 | -5888.0 |
| EIF3F | -5822.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| EIF3K | -5794.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| EIF3H | -5175.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| EIF3J | -5003.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| EIF3I | -4701.0 |
| EIF3E | -4661.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| EIF3L | -4434.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| EIF3M | -3968.0 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| EIF3G | -3720.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| EIF3B | -2321.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| EIF3D | -226.0 |
| RPL27A | 228.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| RPL30 | 1658.0 |
| EIF1AX | 2870.0 |
| RPS9 | 3205.0 |
| RPL12 | 3366.0 |
| EIF3C | 3490.5 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
| EIF3A | 6202.0 |
Peptide chain elongation
| 794 | |
|---|---|
| set | Peptide chain elongation |
| setSize | 67 |
| pANOVA | 4.04e-12 |
| s.dist | -0.49 |
| p.adjustANOVA | 4.6e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| RPL29 | -5888 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| RPS27A | -5344 |
| RPL34 | -5319 |
| RPS8 | -5264 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| RPL29 | -5888.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| EEF1A1 | -2985.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| RPL27A | 228.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| RPL30 | 1658.0 |
| RPS9 | 3205.0 |
| RPL12 | 3366.0 |
| EEF2 | 3968.0 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
Syndecan interactions
| 1181 | |
|---|---|
| set | Syndecan interactions |
| setSize | 19 |
| pANOVA | 0.000268 |
| s.dist | 0.483 |
| p.adjustANOVA | 0.00395 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| THBS1 | 6274 |
| ITGAV | 6242 |
| ITGB3 | 6215 |
| ITGB5 | 6213 |
| ITGB1 | 6188 |
| SDC1 | 6165 |
| ACTN1 | 6122 |
| SDC2 | 4835 |
| FGF2 | 4814 |
| CASK | 4730 |
| ITGA2 | 4663 |
| SDC3 | 2236 |
| ITGB4 | 1902 |
| TNC | 895 |
| ITGA6 | 312 |
| TRAPPC4 | -588 |
| SDC4 | -1091 |
| PRKCA | -3602 |
| TGFB1 | -3726 |
| GeneID | Gene Rank |
|---|---|
| THBS1 | 6274 |
| ITGAV | 6242 |
| ITGB3 | 6215 |
| ITGB5 | 6213 |
| ITGB1 | 6188 |
| SDC1 | 6165 |
| ACTN1 | 6122 |
| SDC2 | 4835 |
| FGF2 | 4814 |
| CASK | 4730 |
| ITGA2 | 4663 |
| SDC3 | 2236 |
| ITGB4 | 1902 |
| TNC | 895 |
| ITGA6 | 312 |
| TRAPPC4 | -588 |
| SDC4 | -1091 |
| PRKCA | -3602 |
| TGFB1 | -3726 |
Eukaryotic Translation Termination
| 346 | |
|---|---|
| set | Eukaryotic Translation Termination |
| setSize | 71 |
| pANOVA | 3.87e-12 |
| s.dist | -0.477 |
| p.adjustANOVA | 4.6e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| RPL29 | -5888 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| TRMT112 | -5408 |
| RPS27A | -5344 |
| RPL34 | -5319 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| RPL29 | -5888.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| TRMT112 | -5408.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| N6AMT1 | -4017.0 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| GSPT2 | -2233.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| RPL27A | 228.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| APEH | 1099.0 |
| RPLP1 | 1114.0 |
| RPL30 | 1658.0 |
| ETF1 | 2208.0 |
| RPS9 | 3205.0 |
| RPL12 | 3366.0 |
| GSPT1 | 3814.0 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
Formation of the ternary complex, and subsequently, the 43S complex
| 391 | |
|---|---|
| set | Formation of the ternary complex, and subsequently, the 43S complex |
| setSize | 47 |
| pANOVA | 1.87e-08 |
| s.dist | -0.474 |
| p.adjustANOVA | 7.52e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS24 | -5953 |
| RPS15 | -5897 |
| EIF2S2 | -5891 |
| EIF3F | -5822 |
| RPS28 | -5799 |
| EIF3K | -5794 |
| RPS26 | -5788 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPS27A | -5344 |
| RPS8 | -5264 |
| EIF3H | -5175 |
| EIF3J | -5003 |
| RPS5 | -4988 |
| RPS17 | -4860 |
| EIF3I | -4701 |
| EIF3E | -4661 |
| RPS19 | -4560 |
| RPS11 | -4469 |
| GeneID | Gene Rank |
|---|---|
| RPS24 | -5953.0 |
| RPS15 | -5897.0 |
| EIF2S2 | -5891.0 |
| EIF3F | -5822.0 |
| RPS28 | -5799.0 |
| EIF3K | -5794.0 |
| RPS26 | -5788.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPS27A | -5344.0 |
| RPS8 | -5264.0 |
| EIF3H | -5175.0 |
| EIF3J | -5003.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| EIF3I | -4701.0 |
| EIF3E | -4661.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| EIF3L | -4434.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| EIF3M | -3968.0 |
| EIF3G | -3720.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| EIF3B | -2321.0 |
| RPS14 | -1992.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| EIF3D | -226.0 |
| EIF2S1 | 150.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| EIF1AX | 2870.0 |
| RPS9 | 3205.0 |
| EIF3C | 3490.5 |
| EIF2S3 | 3918.5 |
| RPS7 | 4000.0 |
| EIF3A | 6202.0 |
Viral mRNA Translation
| 1323 | |
|---|---|
| set | Viral mRNA Translation |
| setSize | 67 |
| pANOVA | 1.99e-11 |
| s.dist | -0.474 |
| p.adjustANOVA | 1.3e-09 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| RPL29 | -5888 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| RPS27A | -5344 |
| RPL34 | -5319 |
| RPS8 | -5264 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| RPL29 | -5888.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| RPL27A | 228.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| RPL30 | 1658.0 |
| GRSF1 | 2246.0 |
| RPS9 | 3205.0 |
| RPL12 | 3366.0 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
| DNAJC3 | 5352.0 |
Telomere C-strand synthesis initiation
| 1234 | |
|---|---|
| set | Telomere C-strand synthesis initiation |
| setSize | 13 |
| pANOVA | 0.00338 |
| s.dist | -0.47 |
| p.adjustANOVA | 0.0282 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ACD | -5901 |
| TERF2 | -5472 |
| CTC1 | -4949 |
| TERF1 | -4726 |
| STN1 | -4087 |
| TERF2IP | -3541 |
| TINF2 | -3162 |
| PRIM2 | -3083 |
| TEN1 | -2887 |
| POT1 | -2620 |
| POLA2 | -289 |
| PRIM1 | 100 |
| POLA1 | 4854 |
| GeneID | Gene Rank |
|---|---|
| ACD | -5901 |
| TERF2 | -5472 |
| CTC1 | -4949 |
| TERF1 | -4726 |
| STN1 | -4087 |
| TERF2IP | -3541 |
| TINF2 | -3162 |
| PRIM2 | -3083 |
| TEN1 | -2887 |
| POT1 | -2620 |
| POLA2 | -289 |
| PRIM1 | 100 |
| POLA1 | 4854 |
Mitochondrial translation initiation
| 659 | |
|---|---|
| set | Mitochondrial translation initiation |
| setSize | 88 |
| pANOVA | 2.75e-14 |
| s.dist | -0.47 |
| p.adjustANOVA | 1.72e-11 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GADD45GIP1 | -5912 |
| MRPS15 | -5890 |
| OXA1L | -5699 |
| MRPS36 | -5678 |
| MRPL32 | -5624 |
| MRPS18A | -5617 |
| MRPS21 | -5554 |
| MRPL41 | -5551 |
| MRPL58 | -5501 |
| MRPL50 | -5449 |
| MRPL38 | -5416 |
| MRPS33 | -5384 |
| MRPL34 | -5342 |
| MRPS18B | -5322 |
| MRPS7 | -5312 |
| MRPL13 | -5304 |
| MRPL48 | -5239 |
| MRPL42 | -5172 |
| MRPL24 | -4977 |
| MRPL14 | -4917 |
| GeneID | Gene Rank |
|---|---|
| GADD45GIP1 | -5912 |
| MRPS15 | -5890 |
| OXA1L | -5699 |
| MRPS36 | -5678 |
| MRPL32 | -5624 |
| MRPS18A | -5617 |
| MRPS21 | -5554 |
| MRPL41 | -5551 |
| MRPL58 | -5501 |
| MRPL50 | -5449 |
| MRPL38 | -5416 |
| MRPS33 | -5384 |
| MRPL34 | -5342 |
| MRPS18B | -5322 |
| MRPS7 | -5312 |
| MRPL13 | -5304 |
| MRPL48 | -5239 |
| MRPL42 | -5172 |
| MRPL24 | -4977 |
| MRPL14 | -4917 |
| MRPS25 | -4909 |
| MRPS5 | -4886 |
| MRPL40 | -4883 |
| MRPL22 | -4800 |
| MRPL4 | -4765 |
| MRPL54 | -4679 |
| MRPS17 | -4655 |
| MRPS2 | -4621 |
| MRPL49 | -4614 |
| MRPL35 | -4568 |
| MRPS16 | -4526 |
| MRPS11 | -4460 |
| MRPL45 | -4336 |
| MRPL18 | -4118 |
| MRPL30 | -3989 |
| CHCHD1 | -3967 |
| MRPS35 | -3962 |
| MRPL1 | -3856 |
| MRPL57 | -3839 |
| MRPL39 | -3788 |
| ERAL1 | -3721 |
| MRPL28 | -3705 |
| MRPL37 | -3521 |
| MRPS26 | -3275 |
| MRPS30 | -3259 |
| MRPL52 | -3221 |
| MRPS18C | -3122 |
| MRPL46 | -3084 |
| MRPL27 | -3002 |
| MRPL11 | -2999 |
| PTCD3 | -2972 |
| MTIF3 | -2956 |
| MRPS22 | -2900 |
| MRPL15 | -2668 |
| MRPS27 | -2637 |
| MRPS10 | -2562 |
| MRPS24 | -2541 |
| MRPS9 | -2157 |
| MRPL17 | -2140 |
| MTIF2 | -2052 |
| MRPL12 | -1893 |
| MRPL43 | -1783 |
| MRPL21 | -1775 |
| AURKAIP1 | -1600 |
| MRPL16 | -1442 |
| MRPS12 | -1225 |
| MTFMT | -1079 |
| MRPS31 | -1051 |
| DAP3 | -992 |
| MRPL51 | -837 |
| MRPL36 | -828 |
| MRPL47 | -221 |
| MRPL10 | -198 |
| MRPS23 | -190 |
| MRPL3 | -97 |
| MRPL2 | 19 |
| MRPL44 | 134 |
| MRPL19 | 468 |
| MRPL55 | 1194 |
| MRPL20 | 1314 |
| MRPL53 | 2111 |
| MRPS14 | 2147 |
| MRPS34 | 2358 |
| MRPL23 | 2639 |
| MRPS28 | 2674 |
| MRPL9 | 4595 |
| MRPL33 | 5054 |
| MRPS6 | 5573 |
Mitochondrial translation termination
| 660 | |
|---|---|
| set | Mitochondrial translation termination |
| setSize | 88 |
| pANOVA | 5.02e-14 |
| s.dist | -0.465 |
| p.adjustANOVA | 1.72e-11 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GADD45GIP1 | -5912 |
| MRPS15 | -5890 |
| OXA1L | -5699 |
| MRPS36 | -5678 |
| MRPL32 | -5624 |
| MRPS18A | -5617 |
| MRPS21 | -5554 |
| MRPL41 | -5551 |
| MRPL58 | -5501 |
| MRPL50 | -5449 |
| MRPL38 | -5416 |
| MRPS33 | -5384 |
| MRPL34 | -5342 |
| MRPS18B | -5322 |
| MRPS7 | -5312 |
| MRPL13 | -5304 |
| MRRF | -5250 |
| MRPL48 | -5239 |
| MRPL42 | -5172 |
| MRPL24 | -4977 |
| GeneID | Gene Rank |
|---|---|
| GADD45GIP1 | -5912 |
| MRPS15 | -5890 |
| OXA1L | -5699 |
| MRPS36 | -5678 |
| MRPL32 | -5624 |
| MRPS18A | -5617 |
| MRPS21 | -5554 |
| MRPL41 | -5551 |
| MRPL58 | -5501 |
| MRPL50 | -5449 |
| MRPL38 | -5416 |
| MRPS33 | -5384 |
| MRPL34 | -5342 |
| MRPS18B | -5322 |
| MRPS7 | -5312 |
| MRPL13 | -5304 |
| MRRF | -5250 |
| MRPL48 | -5239 |
| MRPL42 | -5172 |
| MRPL24 | -4977 |
| MRPL14 | -4917 |
| MRPS25 | -4909 |
| MRPS5 | -4886 |
| MRPL40 | -4883 |
| MRPL22 | -4800 |
| MRPL4 | -4765 |
| MRPL54 | -4679 |
| MRPS17 | -4655 |
| MRPS2 | -4621 |
| MRPL49 | -4614 |
| MRPL35 | -4568 |
| MRPS16 | -4526 |
| MRPS11 | -4460 |
| MRPL45 | -4336 |
| MRPL18 | -4118 |
| MRPL30 | -3989 |
| CHCHD1 | -3967 |
| MRPS35 | -3962 |
| MRPL1 | -3856 |
| MRPL57 | -3839 |
| MRPL39 | -3788 |
| ERAL1 | -3721 |
| MRPL28 | -3705 |
| MRPL37 | -3521 |
| MRPS26 | -3275 |
| MRPS30 | -3259 |
| MRPL52 | -3221 |
| MRPS18C | -3122 |
| MRPL46 | -3084 |
| MRPL27 | -3002 |
| MRPL11 | -2999 |
| PTCD3 | -2972 |
| MRPS22 | -2900 |
| MRPL15 | -2668 |
| MRPS27 | -2637 |
| MRPS10 | -2562 |
| MRPS24 | -2541 |
| MRPS9 | -2157 |
| MRPL17 | -2140 |
| MRPL12 | -1893 |
| MRPL43 | -1783 |
| MRPL21 | -1775 |
| AURKAIP1 | -1600 |
| MRPL16 | -1442 |
| MRPS12 | -1225 |
| MRPS31 | -1051 |
| MTRF1L | -1046 |
| DAP3 | -992 |
| MRPL51 | -837 |
| MRPL36 | -828 |
| MRPL47 | -221 |
| MRPL10 | -198 |
| MRPS23 | -190 |
| MRPL3 | -97 |
| MRPL2 | 19 |
| MRPL44 | 134 |
| MRPL19 | 468 |
| MRPL55 | 1194 |
| MRPL20 | 1314 |
| MRPL53 | 2111 |
| MRPS14 | 2147 |
| MRPS34 | 2358 |
| MRPL23 | 2639 |
| MRPS28 | 2674 |
| GFM2 | 2790 |
| MRPL9 | 4595 |
| MRPL33 | 5054 |
| MRPS6 | 5573 |
Regulation of cholesterol biosynthesis by SREBP (SREBF)
| 982 | |
|---|---|
| set | Regulation of cholesterol biosynthesis by SREBP (SREBF) |
| setSize | 54 |
| pANOVA | 3.89e-09 |
| s.dist | 0.463 |
| p.adjustANOVA | 1.77e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HMGCR | 6265 |
| SCD | 6255 |
| LSS | 6244 |
| SQLE | 6233 |
| INSIG1 | 6198 |
| HMGCS1 | 6164 |
| SEC24D | 6108 |
| CYP51A1 | 6076 |
| IDI1 | 6007 |
| FDPS | 5929 |
| SC5D | 5919 |
| MVD | 5889 |
| SREBF2 | 5879 |
| ACACA | 5851 |
| ELOVL6 | 5643 |
| FASN | 5556 |
| SEC23A | 5487 |
| SEC24A | 5278 |
| MED1 | 5181 |
| KPNB1 | 5121 |
| GeneID | Gene Rank |
|---|---|
| HMGCR | 6265.0 |
| SCD | 6255.0 |
| LSS | 6244.0 |
| SQLE | 6233.0 |
| INSIG1 | 6198.0 |
| HMGCS1 | 6164.0 |
| SEC24D | 6108.0 |
| CYP51A1 | 6076.0 |
| IDI1 | 6007.0 |
| FDPS | 5929.0 |
| SC5D | 5919.0 |
| MVD | 5889.0 |
| SREBF2 | 5879.0 |
| ACACA | 5851.0 |
| ELOVL6 | 5643.0 |
| FASN | 5556.0 |
| SEC23A | 5487.0 |
| SEC24A | 5278.0 |
| MED1 | 5181.0 |
| KPNB1 | 5121.0 |
| MBTPS2 | 5033.0 |
| GPAM | 4848.0 |
| TBL1XR1 | 4666.0 |
| NCOA2 | 4634.0 |
| FDFT1 | 4557.0 |
| INSIG2 | 4551.0 |
| SP1 | 4531.0 |
| HELZ2 | 4486.0 |
| MVK | 4426.0 |
| TM7SF2 | 3914.0 |
| PMVK | 3782.0 |
| DHCR7 | 3729.0 |
| NCOA1 | 3480.0 |
| CREBBP | 3254.0 |
| SREBF1 | 3235.0 |
| SEC24C | 3087.0 |
| NFYB | 2490.0 |
| SEC24B | 1859.0 |
| RAN | 1694.0 |
| NCOA6 | 1610.0 |
| SCAP | 918.0 |
| MTF1 | 889.0 |
| MBTPS1 | 828.0 |
| TBL1X | 449.5 |
| NFYA | -10.0 |
| ACACB | -1102.0 |
| GGPS1 | -2279.0 |
| RXRA | -2529.0 |
| CARM1 | -3430.0 |
| TGS1 | -3595.0 |
| CHD9 | -4625.0 |
| SAR1B | -5183.0 |
| SMARCD3 | -5457.0 |
| NFYC | -5826.0 |
Eukaryotic Translation Elongation
| 344 | |
|---|---|
| set | Eukaryotic Translation Elongation |
| setSize | 70 |
| pANOVA | 4.54e-11 |
| s.dist | -0.455 |
| p.adjustANOVA | 2.82e-09 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| RPL29 | -5888 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| RPS27A | -5344 |
| RPL34 | -5319 |
| RPS8 | -5264 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| RPL29 | -5888.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| EEF1A1 | -2985.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| EEF1D | -506.0 |
| RPL27A | 228.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| RPL30 | 1658.0 |
| EEF1B2 | 2444.0 |
| RPS9 | 3205.0 |
| RPL12 | 3366.0 |
| EEF2 | 3968.0 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| EEF1G | 4387.0 |
| RPL27 | 4941.0 |
Mitochondrial translation elongation
| 658 | |
|---|---|
| set | Mitochondrial translation elongation |
| setSize | 88 |
| pANOVA | 1.93e-13 |
| s.dist | -0.454 |
| p.adjustANOVA | 4.4e-11 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GADD45GIP1 | -5912 |
| MRPS15 | -5890 |
| OXA1L | -5699 |
| MRPS36 | -5678 |
| MRPL32 | -5624 |
| MRPS18A | -5617 |
| MRPS21 | -5554 |
| MRPL41 | -5551 |
| MRPL58 | -5501 |
| MRPL50 | -5449 |
| MRPL38 | -5416 |
| MRPS33 | -5384 |
| MRPL34 | -5342 |
| MRPS18B | -5322 |
| MRPS7 | -5312 |
| MRPL13 | -5304 |
| MRPL48 | -5239 |
| MRPL42 | -5172 |
| MRPL24 | -4977 |
| MRPL14 | -4917 |
| GeneID | Gene Rank |
|---|---|
| GADD45GIP1 | -5912 |
| MRPS15 | -5890 |
| OXA1L | -5699 |
| MRPS36 | -5678 |
| MRPL32 | -5624 |
| MRPS18A | -5617 |
| MRPS21 | -5554 |
| MRPL41 | -5551 |
| MRPL58 | -5501 |
| MRPL50 | -5449 |
| MRPL38 | -5416 |
| MRPS33 | -5384 |
| MRPL34 | -5342 |
| MRPS18B | -5322 |
| MRPS7 | -5312 |
| MRPL13 | -5304 |
| MRPL48 | -5239 |
| MRPL42 | -5172 |
| MRPL24 | -4977 |
| MRPL14 | -4917 |
| MRPS25 | -4909 |
| MRPS5 | -4886 |
| MRPL40 | -4883 |
| MRPL22 | -4800 |
| MRPL4 | -4765 |
| MRPL54 | -4679 |
| MRPS17 | -4655 |
| MRPS2 | -4621 |
| MRPL49 | -4614 |
| MRPL35 | -4568 |
| MRPS16 | -4526 |
| MRPS11 | -4460 |
| MRPL45 | -4336 |
| MRPL18 | -4118 |
| MRPL30 | -3989 |
| CHCHD1 | -3967 |
| MRPS35 | -3962 |
| MRPL1 | -3856 |
| MRPL57 | -3839 |
| MRPL39 | -3788 |
| ERAL1 | -3721 |
| MRPL28 | -3705 |
| MRPL37 | -3521 |
| MRPS26 | -3275 |
| MRPS30 | -3259 |
| MRPL52 | -3221 |
| MRPS18C | -3122 |
| MRPL46 | -3084 |
| MRPL27 | -3002 |
| MRPL11 | -2999 |
| PTCD3 | -2972 |
| MRPS22 | -2900 |
| MRPL15 | -2668 |
| MRPS27 | -2637 |
| MRPS10 | -2562 |
| MRPS24 | -2541 |
| MRPS9 | -2157 |
| MRPL17 | -2140 |
| TUFM | -1941 |
| MRPL12 | -1893 |
| MRPL43 | -1783 |
| MRPL21 | -1775 |
| AURKAIP1 | -1600 |
| MRPL16 | -1442 |
| MRPS12 | -1225 |
| MRPS31 | -1051 |
| DAP3 | -992 |
| MRPL51 | -837 |
| MRPL36 | -828 |
| MRPL47 | -221 |
| MRPL10 | -198 |
| MRPS23 | -190 |
| MRPL3 | -97 |
| MRPL2 | 19 |
| MRPL44 | 134 |
| MRPL19 | 468 |
| GFM1 | 635 |
| MRPL55 | 1194 |
| MRPL20 | 1314 |
| MRPL53 | 2111 |
| MRPS14 | 2147 |
| MRPS34 | 2358 |
| MRPL23 | 2639 |
| MRPS28 | 2674 |
| TSFM | 3679 |
| MRPL9 | 4595 |
| MRPL33 | 5054 |
| MRPS6 | 5573 |
Activation of gene expression by SREBF (SREBP)
| 44 | |
|---|---|
| set | Activation of gene expression by SREBF (SREBP) |
| setSize | 41 |
| pANOVA | 5.14e-07 |
| s.dist | 0.453 |
| p.adjustANOVA | 1.6e-05 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HMGCR | 6265 |
| SCD | 6255 |
| LSS | 6244 |
| SQLE | 6233 |
| HMGCS1 | 6164 |
| CYP51A1 | 6076 |
| IDI1 | 6007 |
| FDPS | 5929 |
| SC5D | 5919 |
| MVD | 5889 |
| SREBF2 | 5879 |
| ACACA | 5851 |
| ELOVL6 | 5643 |
| FASN | 5556 |
| MED1 | 5181 |
| GPAM | 4848 |
| TBL1XR1 | 4666 |
| NCOA2 | 4634 |
| FDFT1 | 4557 |
| SP1 | 4531 |
| GeneID | Gene Rank |
|---|---|
| HMGCR | 6265.0 |
| SCD | 6255.0 |
| LSS | 6244.0 |
| SQLE | 6233.0 |
| HMGCS1 | 6164.0 |
| CYP51A1 | 6076.0 |
| IDI1 | 6007.0 |
| FDPS | 5929.0 |
| SC5D | 5919.0 |
| MVD | 5889.0 |
| SREBF2 | 5879.0 |
| ACACA | 5851.0 |
| ELOVL6 | 5643.0 |
| FASN | 5556.0 |
| MED1 | 5181.0 |
| GPAM | 4848.0 |
| TBL1XR1 | 4666.0 |
| NCOA2 | 4634.0 |
| FDFT1 | 4557.0 |
| SP1 | 4531.0 |
| HELZ2 | 4486.0 |
| MVK | 4426.0 |
| TM7SF2 | 3914.0 |
| PMVK | 3782.0 |
| DHCR7 | 3729.0 |
| NCOA1 | 3480.0 |
| CREBBP | 3254.0 |
| SREBF1 | 3235.0 |
| NFYB | 2490.0 |
| NCOA6 | 1610.0 |
| MTF1 | 889.0 |
| TBL1X | 449.5 |
| NFYA | -10.0 |
| ACACB | -1102.0 |
| GGPS1 | -2279.0 |
| RXRA | -2529.0 |
| CARM1 | -3430.0 |
| TGS1 | -3595.0 |
| CHD9 | -4625.0 |
| SMARCD3 | -5457.0 |
| NFYC | -5826.0 |
Cytosolic tRNA aminoacylation
| 220 | |
|---|---|
| set | Cytosolic tRNA aminoacylation |
| setSize | 24 |
| pANOVA | 0.000128 |
| s.dist | 0.452 |
| p.adjustANOVA | 0.00206 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LARS1 | 6128 |
| NARS1 | 6117 |
| EPRS1 | 6033 |
| IARS1 | 5921 |
| GARS1 | 5813 |
| AARS1 | 5788 |
| WARS1 | 5672 |
| TARS1 | 5651 |
| MARS1 | 5283 |
| CARS1 | 5136 |
| SARS1 | 5048 |
| VARS1 | 4677 |
| DARS1 | 4106 |
| PPA1 | 2766 |
| HARS1 | 2729 |
| FARSB | 2340 |
| YARS1 | 1683 |
| RARS1 | 1448 |
| QARS1 | 768 |
| EEF1E1 | 0 |
| GeneID | Gene Rank |
|---|---|
| LARS1 | 6128 |
| NARS1 | 6117 |
| EPRS1 | 6033 |
| IARS1 | 5921 |
| GARS1 | 5813 |
| AARS1 | 5788 |
| WARS1 | 5672 |
| TARS1 | 5651 |
| MARS1 | 5283 |
| CARS1 | 5136 |
| SARS1 | 5048 |
| VARS1 | 4677 |
| DARS1 | 4106 |
| PPA1 | 2766 |
| HARS1 | 2729 |
| FARSB | 2340 |
| YARS1 | 1683 |
| RARS1 | 1448 |
| QARS1 | 768 |
| EEF1E1 | 0 |
| AIMP1 | -168 |
| FARSA | -3341 |
| AIMP2 | -4776 |
| KARS1 | -5181 |
Selenocysteine synthesis
| 1064 | |
|---|---|
| set | Selenocysteine synthesis |
| setSize | 71 |
| pANOVA | 5.83e-11 |
| s.dist | -0.45 |
| p.adjustANOVA | 3.32e-09 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| RPL29 | -5888 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| RPS27A | -5344 |
| RPL34 | -5319 |
| RPS8 | -5264 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| RPL29 | -5888.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| EEFSEC | -3723.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| PSTK | -1323.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| RPL27A | 228.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| SECISBP2 | 948.0 |
| RPLP1 | 1114.0 |
| RPL30 | 1658.0 |
| SEPHS2 | 2373.0 |
| RPS9 | 3205.0 |
| RPL12 | 3366.0 |
| SEPSECS | 3846.0 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
| SARS1 | 5048.0 |
Abortive elongation of HIV-1 transcript in the absence of Tat
| 27 | |
|---|---|
| set | Abortive elongation of HIV-1 transcript in the absence of Tat |
| setSize | 23 |
| pANOVA | 0.000218 |
| s.dist | -0.445 |
| p.adjustANOVA | 0.00332 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLR2J | -5809 |
| POLR2I | -5691 |
| GTF2F2 | -5685 |
| POLR2E | -5628 |
| POLR2C | -5357 |
| NELFE | -4954 |
| POLR2L | -4936 |
| NELFA | -4597 |
| POLR2D | -4355 |
| GTF2F1 | -4024 |
| NELFCD | -3549 |
| SUPT4H1 | -3123 |
| POLR2F | -2817 |
| SUPT5H | -2128 |
| NCBP1 | -1814 |
| POLR2B | -878 |
| POLR2G | -559 |
| POLR2H | -151 |
| CTDP1 | -130 |
| NCBP2 | 356 |
| GeneID | Gene Rank |
|---|---|
| POLR2J | -5809 |
| POLR2I | -5691 |
| GTF2F2 | -5685 |
| POLR2E | -5628 |
| POLR2C | -5357 |
| NELFE | -4954 |
| POLR2L | -4936 |
| NELFA | -4597 |
| POLR2D | -4355 |
| GTF2F1 | -4024 |
| NELFCD | -3549 |
| SUPT4H1 | -3123 |
| POLR2F | -2817 |
| SUPT5H | -2128 |
| NCBP1 | -1814 |
| POLR2B | -878 |
| POLR2G | -559 |
| POLR2H | -151 |
| CTDP1 | -130 |
| NCBP2 | 356 |
| POLR2A | 820 |
| NELFB | 1534 |
| POLR2K | 3669 |
Mitochondrial translation
| 657 | |
|---|---|
| set | Mitochondrial translation |
| setSize | 94 |
| pANOVA | 1.17e-13 |
| s.dist | -0.443 |
| p.adjustANOVA | 3.2e-11 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GADD45GIP1 | -5912 |
| MRPS15 | -5890 |
| OXA1L | -5699 |
| MRPS36 | -5678 |
| MRPL32 | -5624 |
| MRPS18A | -5617 |
| MRPS21 | -5554 |
| MRPL41 | -5551 |
| MRPL58 | -5501 |
| MRPL50 | -5449 |
| MRPL38 | -5416 |
| MRPS33 | -5384 |
| MRPL34 | -5342 |
| MRPS18B | -5322 |
| MRPS7 | -5312 |
| MRPL13 | -5304 |
| MRRF | -5250 |
| MRPL48 | -5239 |
| MRPL42 | -5172 |
| MRPL24 | -4977 |
| GeneID | Gene Rank |
|---|---|
| GADD45GIP1 | -5912 |
| MRPS15 | -5890 |
| OXA1L | -5699 |
| MRPS36 | -5678 |
| MRPL32 | -5624 |
| MRPS18A | -5617 |
| MRPS21 | -5554 |
| MRPL41 | -5551 |
| MRPL58 | -5501 |
| MRPL50 | -5449 |
| MRPL38 | -5416 |
| MRPS33 | -5384 |
| MRPL34 | -5342 |
| MRPS18B | -5322 |
| MRPS7 | -5312 |
| MRPL13 | -5304 |
| MRRF | -5250 |
| MRPL48 | -5239 |
| MRPL42 | -5172 |
| MRPL24 | -4977 |
| MRPL14 | -4917 |
| MRPS25 | -4909 |
| MRPS5 | -4886 |
| MRPL40 | -4883 |
| MRPL22 | -4800 |
| MRPL4 | -4765 |
| MRPL54 | -4679 |
| MRPS17 | -4655 |
| MRPS2 | -4621 |
| MRPL49 | -4614 |
| MRPL35 | -4568 |
| MRPS16 | -4526 |
| MRPS11 | -4460 |
| MRPL45 | -4336 |
| MRPL18 | -4118 |
| MRPL30 | -3989 |
| CHCHD1 | -3967 |
| MRPS35 | -3962 |
| MRPL1 | -3856 |
| MRPL57 | -3839 |
| MRPL39 | -3788 |
| ERAL1 | -3721 |
| MRPL28 | -3705 |
| MRPL37 | -3521 |
| MRPS26 | -3275 |
| MRPS30 | -3259 |
| MRPL52 | -3221 |
| MRPS18C | -3122 |
| MRPL46 | -3084 |
| MRPL27 | -3002 |
| MRPL11 | -2999 |
| PTCD3 | -2972 |
| MTIF3 | -2956 |
| MRPS22 | -2900 |
| MRPL15 | -2668 |
| MRPS27 | -2637 |
| MRPS10 | -2562 |
| MRPS24 | -2541 |
| MRPS9 | -2157 |
| MRPL17 | -2140 |
| MTIF2 | -2052 |
| TUFM | -1941 |
| MRPL12 | -1893 |
| MRPL43 | -1783 |
| MRPL21 | -1775 |
| AURKAIP1 | -1600 |
| MRPL16 | -1442 |
| MRPS12 | -1225 |
| MTFMT | -1079 |
| MRPS31 | -1051 |
| MTRF1L | -1046 |
| DAP3 | -992 |
| MRPL51 | -837 |
| MRPL36 | -828 |
| MRPL47 | -221 |
| MRPL10 | -198 |
| MRPS23 | -190 |
| MRPL3 | -97 |
| MRPL2 | 19 |
| MRPL44 | 134 |
| MRPL19 | 468 |
| GFM1 | 635 |
| MRPL55 | 1194 |
| MRPL20 | 1314 |
| MRPL53 | 2111 |
| MRPS14 | 2147 |
| MRPS34 | 2358 |
| MRPL23 | 2639 |
| MRPS28 | 2674 |
| GFM2 | 2790 |
| TSFM | 3679 |
| MRPL9 | 4595 |
| MRPL33 | 5054 |
| MRPS6 | 5573 |
MET promotes cell motility
| 613 | |
|---|---|
| set | MET promotes cell motility |
| setSize | 22 |
| pANOVA | 0.000322 |
| s.dist | 0.443 |
| p.adjustANOVA | 0.0046 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ITGB1 | 6188 |
| CRK | 6130 |
| LAMA5 | 5762 |
| LAMB2 | 4913 |
| TNS3 | 4889 |
| ITGA2 | 4663 |
| DOCK7 | 4502 |
| PTK2 | 4333 |
| ITGA3 | 4068 |
| LAMC1 | 4028 |
| CRKL | 3619 |
| LAMC2 | 3528 |
| RAP1B | 3255 |
| LAMB1 | 3200 |
| LAMB3 | 3026 |
| RAPGEF1 | 2987 |
| RAP1A | 2391 |
| SRC | 571 |
| MET | -615 |
| GAB1 | -2146 |
| GeneID | Gene Rank |
|---|---|
| ITGB1 | 6188 |
| CRK | 6130 |
| LAMA5 | 5762 |
| LAMB2 | 4913 |
| TNS3 | 4889 |
| ITGA2 | 4663 |
| DOCK7 | 4502 |
| PTK2 | 4333 |
| ITGA3 | 4068 |
| LAMC1 | 4028 |
| CRKL | 3619 |
| LAMC2 | 3528 |
| RAP1B | 3255 |
| LAMB1 | 3200 |
| LAMB3 | 3026 |
| RAPGEF1 | 2987 |
| RAP1A | 2391 |
| SRC | 571 |
| MET | -615 |
| GAB1 | -2146 |
| GRB2 | -2780 |
| RAC1 | -3833 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
| 730 | |
|---|---|
| set | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
| setSize | 72 |
| pANOVA | 9.27e-11 |
| s.dist | -0.442 |
| p.adjustANOVA | 4.88e-09 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| RPL29 | -5888 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| RPS27A | -5344 |
| RPL34 | -5319 |
| RPS8 | -5264 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| RPL29 | -5888.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| GSPT2 | -2233.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| NCBP1 | -1814.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| UPF1 | -158.0 |
| RPL27A | 228.0 |
| NCBP2 | 356.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| RPL30 | 1658.0 |
| ETF1 | 2208.0 |
| RPS9 | 3205.0 |
| RPL12 | 3366.0 |
| GSPT1 | 3814.0 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
| EIF4G1 | 5853.0 |
Response of EIF2AK1 (HRI) to heme deficiency
| 1009 | |
|---|---|
| set | Response of EIF2AK1 (HRI) to heme deficiency |
| setSize | 15 |
| pANOVA | 0.00312 |
| s.dist | 0.441 |
| p.adjustANOVA | 0.0273 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TRIB3 | 6160.0 |
| ATF5 | 6121.0 |
| ASNS | 5840.0 |
| DDIT3 | 5702.0 |
| CHAC1 | 5633.0 |
| CEBPG | 5332.0 |
| CEBPB | 5272.0 |
| ATF4 | 4221.0 |
| EIF2S3 | 3918.5 |
| ATF3 | 2974.0 |
| PPP1R15A | 421.0 |
| EIF2S1 | 150.0 |
| GRB10 | -889.0 |
| EIF2AK1 | -2403.0 |
| EIF2S2 | -5891.0 |
| GeneID | Gene Rank |
|---|---|
| TRIB3 | 6160.0 |
| ATF5 | 6121.0 |
| ASNS | 5840.0 |
| DDIT3 | 5702.0 |
| CHAC1 | 5633.0 |
| CEBPG | 5332.0 |
| CEBPB | 5272.0 |
| ATF4 | 4221.0 |
| EIF2S3 | 3918.5 |
| ATF3 | 2974.0 |
| PPP1R15A | 421.0 |
| EIF2S1 | 150.0 |
| GRB10 | -889.0 |
| EIF2AK1 | -2403.0 |
| EIF2S2 | -5891.0 |
Assembly Of The HIV Virion
| 77 | |
|---|---|
| set | Assembly Of The HIV Virion |
| setSize | 16 |
| pANOVA | 0.00228 |
| s.dist | -0.441 |
| p.adjustANOVA | 0.0221 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UBA52 | -5753 |
| TSG101 | -5714 |
| VPS28 | -5424 |
| RPS27A | -5344 |
| UBAP1 | -5098 |
| UBB | -4930 |
| MVB12A | -4676 |
| NMT2 | -3113 |
| VPS37B | -2145 |
| MVB12B | -2090 |
| VPS37D | -2032 |
| PPIA | -1695 |
| VPS37C | -607 |
| UBC | 1127 |
| FURIN | 1648 |
| VPS37A | 4688 |
| GeneID | Gene Rank |
|---|---|
| UBA52 | -5753 |
| TSG101 | -5714 |
| VPS28 | -5424 |
| RPS27A | -5344 |
| UBAP1 | -5098 |
| UBB | -4930 |
| MVB12A | -4676 |
| NMT2 | -3113 |
| VPS37B | -2145 |
| MVB12B | -2090 |
| VPS37D | -2032 |
| PPIA | -1695 |
| VPS37C | -607 |
| UBC | 1127 |
| FURIN | 1648 |
| VPS37A | 4688 |
Complex I biogenesis
| 192 | |
|---|---|
| set | Complex I biogenesis |
| setSize | 56 |
| pANOVA | 1.28e-08 |
| s.dist | -0.44 |
| p.adjustANOVA | 5.46e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MT-ND6 | -6005 |
| MT-ND2 | -5987 |
| MT-ND4 | -5978 |
| MT-ND1 | -5971 |
| NDUFV2 | -5915 |
| NDUFA11 | -5874 |
| NDUFA3 | -5866 |
| NDUFV3 | -5836 |
| NDUFA13 | -5619 |
| NDUFB7 | -5493 |
| MT-ND5 | -5464 |
| NDUFA6 | -5306 |
| NDUFB5 | -5265 |
| NDUFS8 | -5180 |
| NDUFS7 | -4978 |
| NDUFB9 | -4924 |
| MT-ND3 | -4901 |
| NDUFA10 | -4856 |
| NDUFA12 | -4842 |
| NDUFB4 | -4693 |
| GeneID | Gene Rank |
|---|---|
| MT-ND6 | -6005 |
| MT-ND2 | -5987 |
| MT-ND4 | -5978 |
| MT-ND1 | -5971 |
| NDUFV2 | -5915 |
| NDUFA11 | -5874 |
| NDUFA3 | -5866 |
| NDUFV3 | -5836 |
| NDUFA13 | -5619 |
| NDUFB7 | -5493 |
| MT-ND5 | -5464 |
| NDUFA6 | -5306 |
| NDUFB5 | -5265 |
| NDUFS8 | -5180 |
| NDUFS7 | -4978 |
| NDUFB9 | -4924 |
| MT-ND3 | -4901 |
| NDUFA10 | -4856 |
| NDUFA12 | -4842 |
| NDUFB4 | -4693 |
| NDUFB11 | -4524 |
| NDUFA8 | -4491 |
| NDUFC2 | -4102 |
| NDUFB10 | -3868 |
| NDUFAF4 | -3756 |
| NDUFA5 | -3615 |
| NDUFS6 | -3410 |
| NDUFS4 | -3320 |
| NDUFS3 | -3100 |
| NDUFS2 | -3008 |
| TMEM126B | -2988 |
| NDUFA7 | -2945 |
| NDUFAB1 | -2890 |
| NDUFC1 | -2749 |
| NDUFAF1 | -2451 |
| NDUFAF2 | -2392 |
| ECSIT | -2378 |
| NDUFS5 | -2352 |
| NDUFAF3 | -1702 |
| NDUFB1 | -1127 |
| NDUFAF6 | -888 |
| NDUFA2 | -569 |
| NDUFB6 | 82 |
| NDUFAF5 | 179 |
| NDUFB8 | 335 |
| TMEM186 | 564 |
| NDUFAF7 | 687 |
| NDUFB3 | 1088 |
| ACAD9 | 1581 |
| TIMMDC1 | 2131 |
| NDUFA9 | 2631 |
| NUBPL | 2825 |
| NDUFV1 | 2861 |
| NDUFB2 | 4017 |
| NDUFS1 | 4255 |
| NDUFA1 | 5094 |
SARS-CoV-2 modulates host translation machinery
| 1026 | |
|---|---|
| set | SARS-CoV-2 modulates host translation machinery |
| setSize | 45 |
| pANOVA | 3.63e-07 |
| s.dist | -0.438 |
| p.adjustANOVA | 1.21e-05 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS24 | -5953.0 |
| RPS15 | -5897.0 |
| RPS28 | -5799.0 |
| RPS26 | -5788.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPS27A | -5344.0 |
| RPS8 | -5264.0 |
| SNRPG | -5207.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| GEMIN8 | -4817.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| SNRPD1 | -4225.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| GEMIN7 | -3672.0 |
| GeneID | Gene Rank |
|---|---|
| RPS24 | -5953.0 |
| RPS15 | -5897.0 |
| RPS28 | -5799.0 |
| RPS26 | -5788.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPS27A | -5344.0 |
| RPS8 | -5264.0 |
| SNRPG | -5207.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| GEMIN8 | -4817.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| SNRPD1 | -4225.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| GEMIN7 | -3672.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| SNRPD3 | -3139.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| SNRPD2 | -2742.0 |
| RPS14 | -1992.0 |
| DDX20 | -1828.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| GEMIN6 | -1197.0 |
| GEMIN4 | -1120.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| SNRPF | 210.0 |
| SMN1 | 508.5 |
| SNRPE | 697.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| SNRPB | 999.0 |
| GEMIN2 | 1565.0 |
| RPS9 | 3205.0 |
| RPS7 | 4000.0 |
| GEMIN5 | 4265.0 |
Regulation of innate immune responses to cytosolic DNA
| 986 | |
|---|---|
| set | Regulation of innate immune responses to cytosolic DNA |
| setSize | 13 |
| pANOVA | 0.00651 |
| s.dist | -0.436 |
| p.adjustANOVA | 0.042 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UBA52 | -5753 |
| RPS27A | -5344 |
| DTX4 | -5231 |
| IRF3 | -5168 |
| TREX1 | -5042 |
| UBB | -4930 |
| STING1 | -4844 |
| DDX41 | -4648 |
| TRIM32 | -3116 |
| TRIM21 | -611 |
| UBC | 1127 |
| TBK1 | 4524 |
| TRIM56 | 5963 |
| GeneID | Gene Rank |
|---|---|
| UBA52 | -5753 |
| RPS27A | -5344 |
| DTX4 | -5231 |
| IRF3 | -5168 |
| TREX1 | -5042 |
| UBB | -4930 |
| STING1 | -4844 |
| DDX41 | -4648 |
| TRIM32 | -3116 |
| TRIM21 | -611 |
| UBC | 1127 |
| TBK1 | 4524 |
| TRIM56 | 5963 |
Kinesins
| 582 | |
|---|---|
| set | Kinesins |
| setSize | 36 |
| pANOVA | 6.46e-06 |
| s.dist | 0.435 |
| p.adjustANOVA | 0.000164 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KIF1B | 6151 |
| KIF5B | 6082 |
| KIF1C | 6034 |
| KIF21B | 6031 |
| KLC1 | 5992 |
| KIF26B | 5990 |
| CENPE | 5574 |
| KIFC1 | 5482 |
| KIF11 | 5274 |
| KIF21A | 5247 |
| KIF3B | 5158 |
| KIF4A | 5133 |
| RACGAP1 | 5020 |
| KIF13B | 4976 |
| KIF3C | 4961 |
| KIF20B | 4904 |
| KIF15 | 3906 |
| KIF2C | 3666 |
| KIF5C | 3170 |
| KIF18B | 3159 |
| GeneID | Gene Rank |
|---|---|
| KIF1B | 6151 |
| KIF5B | 6082 |
| KIF1C | 6034 |
| KIF21B | 6031 |
| KLC1 | 5992 |
| KIF26B | 5990 |
| CENPE | 5574 |
| KIFC1 | 5482 |
| KIF11 | 5274 |
| KIF21A | 5247 |
| KIF3B | 5158 |
| KIF4A | 5133 |
| RACGAP1 | 5020 |
| KIF13B | 4976 |
| KIF3C | 4961 |
| KIF20B | 4904 |
| KIF15 | 3906 |
| KIF2C | 3666 |
| KIF5C | 3170 |
| KIF18B | 3159 |
| KIF23 | 3030 |
| KIF22 | 2792 |
| KIF20A | 2719 |
| KLC2 | 2242 |
| KIF1A | 2081 |
| KIF6 | 1506 |
| KIFAP3 | 1493 |
| KIF2A | 1000 |
| KIF5A | 415 |
| KIF18A | 126 |
| KIF9 | -116 |
| KLC4 | -2578 |
| KIFC2 | -3570 |
| KLC3 | -3784 |
| KIF3A | -4342 |
| KIF12 | -4343 |
PKA activation
| 778 | |
|---|---|
| set | PKA activation |
| setSize | 13 |
| pANOVA | 0.00668 |
| s.dist | 0.435 |
| p.adjustANOVA | 0.0421 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ADCY9 | 5909 |
| ADCY7 | 5655 |
| ADCY1 | 5543 |
| NBEA | 5494 |
| PRKAR2B | 5316 |
| PRKAR1A | 4931 |
| ADCY6 | 4412 |
| ADCY3 | 3151 |
| PRKAR2A | 2848 |
| PRKAR1B | 388 |
| PRKACB | -446 |
| CALM1 | -1598 |
| PRKACA | -5220 |
| GeneID | Gene Rank |
|---|---|
| ADCY9 | 5909 |
| ADCY7 | 5655 |
| ADCY1 | 5543 |
| NBEA | 5494 |
| PRKAR2B | 5316 |
| PRKAR1A | 4931 |
| ADCY6 | 4412 |
| ADCY3 | 3151 |
| PRKAR2A | 2848 |
| PRKAR1B | 388 |
| PRKACB | -446 |
| CALM1 | -1598 |
| PRKACA | -5220 |
L13a-mediated translational silencing of Ceruloplasmin expression
| 583 | |
|---|---|
| set | L13a-mediated translational silencing of Ceruloplasmin expression |
| setSize | 88 |
| pANOVA | 6.67e-12 |
| s.dist | -0.424 |
| p.adjustANOVA | 5.98e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| EIF2S2 | -5891 |
| RPL29 | -5888 |
| EIF3F | -5822 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| EIF3K | -5794 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| EIF2S2 | -5891.0 |
| RPL29 | -5888.0 |
| EIF3F | -5822.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| EIF3K | -5794.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| EIF3H | -5175.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| EIF3J | -5003.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| EIF3I | -4701.0 |
| EIF3E | -4661.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| EIF3L | -4434.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| EIF3M | -3968.0 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| EIF3G | -3720.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| EIF3B | -2321.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| EIF4H | -577.0 |
| EIF3D | -226.0 |
| EIF2S1 | 150.0 |
| EIF4E | 207.0 |
| RPL27A | 228.0 |
| EIF4A1 | 285.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| RPL30 | 1658.0 |
| EIF1AX | 2870.0 |
| EIF4B | 2984.0 |
| RPS9 | 3205.0 |
| EIF4A2 | 3322.0 |
| RPL12 | 3366.0 |
| EIF3C | 3490.5 |
| EIF2S3 | 3918.5 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
| EIF4G1 | 5853.0 |
| EIF3A | 6202.0 |
GTP hydrolysis and joining of the 60S ribosomal subunit
| 427 | |
|---|---|
| set | GTP hydrolysis and joining of the 60S ribosomal subunit |
| setSize | 90 |
| pANOVA | 6.99e-12 |
| s.dist | -0.419 |
| p.adjustANOVA | 5.98e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| EIF2S2 | -5891 |
| RPL29 | -5888 |
| EIF3F | -5822 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| EIF3K | -5794 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| EIF2S2 | -5891.0 |
| RPL29 | -5888.0 |
| EIF3F | -5822.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| EIF3K | -5794.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| EIF5B | -5385.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| EIF3H | -5175.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| EIF3J | -5003.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| EIF3I | -4701.0 |
| EIF3E | -4661.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| EIF3L | -4434.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| EIF3M | -3968.0 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| EIF3G | -3720.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| EIF3B | -2321.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| EIF4H | -577.0 |
| EIF3D | -226.0 |
| EIF2S1 | 150.0 |
| EIF4E | 207.0 |
| RPL27A | 228.0 |
| EIF4A1 | 285.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| RPL30 | 1658.0 |
| EIF1AX | 2870.0 |
| EIF4B | 2984.0 |
| RPS9 | 3205.0 |
| EIF4A2 | 3322.0 |
| EIF5 | 3324.0 |
| RPL12 | 3366.0 |
| EIF3C | 3490.5 |
| EIF2S3 | 3918.5 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
| EIF4G1 | 5853.0 |
| EIF3A | 6202.0 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
| 729 | |
|---|---|
| set | Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) |
| setSize | 92 |
| pANOVA | 5.54e-12 |
| s.dist | -0.416 |
| p.adjustANOVA | 5.41e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| RPL29 | -5888 |
| PPP2R1A | -5860 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| RPS26 | -5788 |
| UPF3B | -5787 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| MAGOH | -5409 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| RPL29 | -5888.0 |
| PPP2R1A | -5860.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| RPS26 | -5788.0 |
| UPF3B | -5787.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| MAGOH | -5409.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| PNRC2 | -5229.0 |
| RNPS1 | -5170.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| UPF2 | -4673.0 |
| RPS19 | -4560.0 |
| RBM8A | -4527.0 |
| RPS11 | -4469.0 |
| EIF4A3 | -4351.0 |
| RPS20 | -4177.0 |
| PPP2CA | -4168.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| PPP2R2A | -3870.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| SMG9 | -3333.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| GSPT2 | -2233.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| CASC3 | -1901.0 |
| RPL23 | -1859.0 |
| NCBP1 | -1814.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| UPF1 | -158.0 |
| SMG6 | 137.0 |
| RPL27A | 228.0 |
| NCBP2 | 356.0 |
| RPL8 | 395.0 |
| SMG7 | 560.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| UPF3A | 1159.0 |
| DCP1A | 1181.0 |
| SMG8 | 1620.0 |
| RPL30 | 1658.0 |
| ETF1 | 2208.0 |
| RPS9 | 3205.0 |
| RPL12 | 3366.0 |
| MAGOHB | 3470.0 |
| SMG5 | 3605.0 |
| GSPT1 | 3814.0 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
| EIF4G1 | 5853.0 |
| SMG1 | 6064.0 |
Nonsense-Mediated Decay (NMD)
| 731 | |
|---|---|
| set | Nonsense-Mediated Decay (NMD) |
| setSize | 92 |
| pANOVA | 5.54e-12 |
| s.dist | -0.416 |
| p.adjustANOVA | 5.41e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| RPL29 | -5888 |
| PPP2R1A | -5860 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| RPS26 | -5788 |
| UPF3B | -5787 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| MAGOH | -5409 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| RPL29 | -5888.0 |
| PPP2R1A | -5860.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| RPS26 | -5788.0 |
| UPF3B | -5787.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| MAGOH | -5409.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| PNRC2 | -5229.0 |
| RNPS1 | -5170.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| UPF2 | -4673.0 |
| RPS19 | -4560.0 |
| RBM8A | -4527.0 |
| RPS11 | -4469.0 |
| EIF4A3 | -4351.0 |
| RPS20 | -4177.0 |
| PPP2CA | -4168.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| PPP2R2A | -3870.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| SMG9 | -3333.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| GSPT2 | -2233.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| CASC3 | -1901.0 |
| RPL23 | -1859.0 |
| NCBP1 | -1814.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| UPF1 | -158.0 |
| SMG6 | 137.0 |
| RPL27A | 228.0 |
| NCBP2 | 356.0 |
| RPL8 | 395.0 |
| SMG7 | 560.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| UPF3A | 1159.0 |
| DCP1A | 1181.0 |
| SMG8 | 1620.0 |
| RPL30 | 1658.0 |
| ETF1 | 2208.0 |
| RPS9 | 3205.0 |
| RPL12 | 3366.0 |
| MAGOHB | 3470.0 |
| SMG5 | 3605.0 |
| GSPT1 | 3814.0 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
| EIF4G1 | 5853.0 |
| SMG1 | 6064.0 |
CLEC7A (Dectin-1) induces NFAT activation
| 115 | |
|---|---|
| set | CLEC7A (Dectin-1) induces NFAT activation |
| setSize | 10 |
| pANOVA | 0.0232 |
| s.dist | 0.415 |
| p.adjustANOVA | 0.106 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ITPR2 | 5973 |
| ITPR3 | 5960 |
| AHCYL1 | 5616 |
| ITPR1 | 5565 |
| PPP3R1 | 4155 |
| NFATC3 | 2933 |
| NFATC1 | 1659 |
| PPP3CB | 88 |
| CALM1 | -1598 |
| PPP3CA | -3579 |
| GeneID | Gene Rank |
|---|---|
| ITPR2 | 5973 |
| ITPR3 | 5960 |
| AHCYL1 | 5616 |
| ITPR1 | 5565 |
| PPP3R1 | 4155 |
| NFATC3 | 2933 |
| NFATC1 | 1659 |
| PPP3CB | 88 |
| CALM1 | -1598 |
| PPP3CA | -3579 |
Chondroitin sulfate biosynthesis
| 169 | |
|---|---|
| set | Chondroitin sulfate biosynthesis |
| setSize | 16 |
| pANOVA | 0.00488 |
| s.dist | 0.407 |
| p.adjustANOVA | 0.0351 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CSGALNACT1 | 6105 |
| VCAN | 6096 |
| BGN | 5927 |
| CHPF2 | 5792 |
| CSGALNACT2 | 5645 |
| CSPG4 | 5552 |
| CHSY3 | 5349 |
| CHST11 | 4720 |
| CHSY1 | 4399 |
| CHST7 | 3210 |
| CHPF | 2865 |
| CHST12 | -792 |
| CHST15 | -1758 |
| NCAN | -2240 |
| CSPG5 | -2944 |
| DCN | -5906 |
| GeneID | Gene Rank |
|---|---|
| CSGALNACT1 | 6105 |
| VCAN | 6096 |
| BGN | 5927 |
| CHPF2 | 5792 |
| CSGALNACT2 | 5645 |
| CSPG4 | 5552 |
| CHSY3 | 5349 |
| CHST11 | 4720 |
| CHSY1 | 4399 |
| CHST7 | 3210 |
| CHPF | 2865 |
| CHST12 | -792 |
| CHST15 | -1758 |
| NCAN | -2240 |
| CSPG5 | -2944 |
| DCN | -5906 |
Non-integrin membrane-ECM interactions
| 727 | |
|---|---|
| set | Non-integrin membrane-ECM interactions |
| setSize | 34 |
| pANOVA | 4.44e-05 |
| s.dist | 0.405 |
| p.adjustANOVA | 0.00082 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| THBS1 | 6274 |
| ITGAV | 6242 |
| ITGB3 | 6215 |
| ITGB5 | 6213 |
| ITGB1 | 6188 |
| SDC1 | 6165 |
| ACTN1 | 6122 |
| HSPG2 | 5946 |
| LAMA5 | 5762 |
| DAG1 | 5506 |
| LAMB2 | 4913 |
| NTN4 | 4886 |
| DDR2 | 4884 |
| SDC2 | 4835 |
| FGF2 | 4814 |
| CASK | 4730 |
| ITGA2 | 4663 |
| LAMC1 | 4028 |
| LAMC2 | 3528 |
| LAMB1 | 3200 |
| GeneID | Gene Rank |
|---|---|
| THBS1 | 6274 |
| ITGAV | 6242 |
| ITGB3 | 6215 |
| ITGB5 | 6213 |
| ITGB1 | 6188 |
| SDC1 | 6165 |
| ACTN1 | 6122 |
| HSPG2 | 5946 |
| LAMA5 | 5762 |
| DAG1 | 5506 |
| LAMB2 | 4913 |
| NTN4 | 4886 |
| DDR2 | 4884 |
| SDC2 | 4835 |
| FGF2 | 4814 |
| CASK | 4730 |
| ITGA2 | 4663 |
| LAMC1 | 4028 |
| LAMC2 | 3528 |
| LAMB1 | 3200 |
| LAMB3 | 3026 |
| SDC3 | 2236 |
| ITGB4 | 1902 |
| DMD | 1711 |
| TNC | 895 |
| ITGA6 | 312 |
| TRAPPC4 | -588 |
| SDC4 | -1091 |
| PDGFB | -2730 |
| PRKCA | -3602 |
| AGRN | -3712 |
| TGFB1 | -3726 |
| DDR1 | -5458 |
| PDGFA | -5479 |
HS-GAG degradation
| 481 | |
|---|---|
| set | HS-GAG degradation |
| setSize | 18 |
| pANOVA | 0.00304 |
| s.dist | 0.404 |
| p.adjustANOVA | 0.0268 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SDC1 | 6165 |
| GPC1 | 6084 |
| HSPG2 | 5946 |
| IDS | 5392 |
| SDC2 | 4835 |
| GPC4 | 4640 |
| HPSE | 4513 |
| GPC6 | 4261 |
| GLB1L | 3635 |
| SGSH | 2791 |
| SDC3 | 2236 |
| GUSB | 2216 |
| NAGLU | 1682 |
| GLB1 | 153 |
| IDUA | -144 |
| SDC4 | -1091 |
| GPC2 | -2665 |
| AGRN | -3712 |
| GeneID | Gene Rank |
|---|---|
| SDC1 | 6165 |
| GPC1 | 6084 |
| HSPG2 | 5946 |
| IDS | 5392 |
| SDC2 | 4835 |
| GPC4 | 4640 |
| HPSE | 4513 |
| GPC6 | 4261 |
| GLB1L | 3635 |
| SGSH | 2791 |
| SDC3 | 2236 |
| GUSB | 2216 |
| NAGLU | 1682 |
| GLB1 | 153 |
| IDUA | -144 |
| SDC4 | -1091 |
| GPC2 | -2665 |
| AGRN | -3712 |
Formation of ATP by chemiosmotic coupling
| 377 | |
|---|---|
| set | Formation of ATP by chemiosmotic coupling |
| setSize | 17 |
| pANOVA | 0.00405 |
| s.dist | -0.403 |
| p.adjustANOVA | 0.0316 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MT-ATP8 | -5958.0 |
| MT-ATP6 | -5894.0 |
| ATP5PO | -5740.0 |
| ATP5MF | -5647.0 |
| ATP5PD | -5492.0 |
| ATP5F1C | -5406.0 |
| ATP5PF | -5234.0 |
| ATP5F1D | -5149.0 |
| ATP5F1A | -3283.0 |
| DMAC2L | -1313.0 |
| ATP5ME | -738.0 |
| ATP5MG | -662.5 |
| ATP5PB | -164.0 |
| ATP5F1B | -36.0 |
| ATP5F1E | 1759.0 |
| ATP5MC3 | 3583.0 |
| ATP5MC2 | 5593.0 |
| GeneID | Gene Rank |
|---|---|
| MT-ATP8 | -5958.0 |
| MT-ATP6 | -5894.0 |
| ATP5PO | -5740.0 |
| ATP5MF | -5647.0 |
| ATP5PD | -5492.0 |
| ATP5F1C | -5406.0 |
| ATP5PF | -5234.0 |
| ATP5F1D | -5149.0 |
| ATP5F1A | -3283.0 |
| DMAC2L | -1313.0 |
| ATP5ME | -738.0 |
| ATP5MG | -662.5 |
| ATP5PB | -164.0 |
| ATP5F1B | -36.0 |
| ATP5F1E | 1759.0 |
| ATP5MC3 | 3583.0 |
| ATP5MC2 | 5593.0 |
Signaling by FLT3 fusion proteins
| 1115 | |
|---|---|
| set | Signaling by FLT3 fusion proteins |
| setSize | 19 |
| pANOVA | 0.00242 |
| s.dist | 0.402 |
| p.adjustANOVA | 0.0229 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TRIP11 | 6037 |
| GOLGB1 | 5982 |
| SPTBN1 | 5605 |
| NOX4 | 5323 |
| PIK3R1 | 5067 |
| GAB2 | 4838 |
| PIM1 | 4515 |
| SOS1 | 4483 |
| MYO18A | 4036 |
| KRAS | 3661 |
| ZMYM2 | 3417 |
| ETV6 | 2471 |
| PIK3CA | 2430 |
| NRAS | 1310 |
| STAT5B | 1228 |
| STAT5A | 505 |
| GRB2 | -2780 |
| HRAS | -3032 |
| CDKN1A | -5732 |
| GeneID | Gene Rank |
|---|---|
| TRIP11 | 6037 |
| GOLGB1 | 5982 |
| SPTBN1 | 5605 |
| NOX4 | 5323 |
| PIK3R1 | 5067 |
| GAB2 | 4838 |
| PIM1 | 4515 |
| SOS1 | 4483 |
| MYO18A | 4036 |
| KRAS | 3661 |
| ZMYM2 | 3417 |
| ETV6 | 2471 |
| PIK3CA | 2430 |
| NRAS | 1310 |
| STAT5B | 1228 |
| STAT5A | 505 |
| GRB2 | -2780 |
| HRAS | -3032 |
| CDKN1A | -5732 |
Nephrin family interactions
| 714 | |
|---|---|
| set | Nephrin family interactions |
| setSize | 19 |
| pANOVA | 0.00243 |
| s.dist | 0.402 |
| p.adjustANOVA | 0.0229 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ACTN1 | 6122 |
| IQGAP1 | 6055 |
| SPTBN1 | 5605 |
| PIK3CB | 5551 |
| SPTAN1 | 5176 |
| PIK3R1 | 5067 |
| KIRREL3 | 5058 |
| CASK | 4730 |
| NCK2 | 2770 |
| ACTN4 | 2591 |
| PIK3CA | 2430 |
| ACTN3 | 1591 |
| FYN | 540 |
| MAGI2 | 297 |
| CD2AP | -46 |
| ACTN2 | -73 |
| NCK1 | -413 |
| WASL | -902 |
| PIK3R2 | -2798 |
| GeneID | Gene Rank |
|---|---|
| ACTN1 | 6122 |
| IQGAP1 | 6055 |
| SPTBN1 | 5605 |
| PIK3CB | 5551 |
| SPTAN1 | 5176 |
| PIK3R1 | 5067 |
| KIRREL3 | 5058 |
| CASK | 4730 |
| NCK2 | 2770 |
| ACTN4 | 2591 |
| PIK3CA | 2430 |
| ACTN3 | 1591 |
| FYN | 540 |
| MAGI2 | 297 |
| CD2AP | -46 |
| ACTN2 | -73 |
| NCK1 | -413 |
| WASL | -902 |
| PIK3R2 | -2798 |
Collagen chain trimerization
| 187 | |
|---|---|
| set | Collagen chain trimerization |
| setSize | 26 |
| pANOVA | 0.000418 |
| s.dist | 0.4 |
| p.adjustANOVA | 0.00578 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| COL1A2 | 6276 |
| COL5A2 | 6238 |
| COL6A3 | 6192 |
| COL1A1 | 6156 |
| COL12A1 | 6124 |
| COL16A1 | 6025 |
| COL6A2 | 5967 |
| COL5A1 | 5956 |
| COL4A5 | 5823 |
| COL5A3 | 5734 |
| COL2A1 | 5384 |
| COL4A4 | 5329 |
| COL6A1 | 5145 |
| COL11A2 | 5089 |
| COL18A1 | 3647 |
| COL4A3 | 3484 |
| COL20A1 | 3218 |
| COL8A2 | 2527 |
| COL26A1 | 1536 |
| COL3A1 | -9 |
| GeneID | Gene Rank |
|---|---|
| COL1A2 | 6276 |
| COL5A2 | 6238 |
| COL6A3 | 6192 |
| COL1A1 | 6156 |
| COL12A1 | 6124 |
| COL16A1 | 6025 |
| COL6A2 | 5967 |
| COL5A1 | 5956 |
| COL4A5 | 5823 |
| COL5A3 | 5734 |
| COL2A1 | 5384 |
| COL4A4 | 5329 |
| COL6A1 | 5145 |
| COL11A2 | 5089 |
| COL18A1 | 3647 |
| COL4A3 | 3484 |
| COL20A1 | 3218 |
| COL8A2 | 2527 |
| COL26A1 | 1536 |
| COL3A1 | -9 |
| COL27A1 | -3438 |
| COL4A2 | -3561 |
| COL4A1 | -5010 |
| COL4A6 | -5080 |
| COL8A1 | -5598 |
| COL11A1 | -5983 |
Elastic fibre formation
| 332 | |
|---|---|
| set | Elastic fibre formation |
| setSize | 31 |
| pANOVA | 0.000119 |
| s.dist | 0.399 |
| p.adjustANOVA | 0.00194 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| FBN1 | 6271 |
| ITGAV | 6242 |
| ITGB3 | 6215 |
| ITGB5 | 6213 |
| ITGB1 | 6188 |
| LOX | 6044 |
| LOXL4 | 6022 |
| FBLN2 | 5941 |
| LOXL2 | 5806 |
| FBLN5 | 5520 |
| LTBP1 | 5500 |
| LOXL3 | 5256 |
| FBLN1 | 5078 |
| ITGA5 | 4809 |
| LTBP2 | 3935 |
| TGFB3 | 3930 |
| EFEMP1 | 3620 |
| BMP4 | 3364 |
| ITGB8 | 3237 |
| LTBP3 | 3070 |
| GeneID | Gene Rank |
|---|---|
| FBN1 | 6271 |
| ITGAV | 6242 |
| ITGB3 | 6215 |
| ITGB5 | 6213 |
| ITGB1 | 6188 |
| LOX | 6044 |
| LOXL4 | 6022 |
| FBLN2 | 5941 |
| LOXL2 | 5806 |
| FBLN5 | 5520 |
| LTBP1 | 5500 |
| LOXL3 | 5256 |
| FBLN1 | 5078 |
| ITGA5 | 4809 |
| LTBP2 | 3935 |
| TGFB3 | 3930 |
| EFEMP1 | 3620 |
| BMP4 | 3364 |
| ITGB8 | 3237 |
| LTBP3 | 3070 |
| BMP7 | 2857 |
| FURIN | 1648 |
| TGFB2 | 1313 |
| EFEMP2 | 935 |
| LOXL1 | -2597 |
| TGFB1 | -3726 |
| MFAP3 | -3953 |
| ELN | -4128 |
| MFAP2 | -4174 |
| ITGB6 | -4784 |
| LTBP4 | -5680 |
Cap-dependent Translation Initiation
| 135 | |
|---|---|
| set | Cap-dependent Translation Initiation |
| setSize | 96 |
| pANOVA | 1.41e-11 |
| s.dist | -0.399 |
| p.adjustANOVA | 9.73e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| EIF2S2 | -5891 |
| RPL29 | -5888 |
| EIF3F | -5822 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| EIF3K | -5794 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| EIF2S2 | -5891.0 |
| RPL29 | -5888.0 |
| EIF3F | -5822.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| EIF3K | -5794.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| EIF5B | -5385.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| EIF3H | -5175.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| EIF3J | -5003.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| EIF3I | -4701.0 |
| EIF3E | -4661.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| EIF3L | -4434.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| EIF3M | -3968.0 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| EIF3G | -3720.0 |
| EIF2B4 | -3530.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| EIF3B | -2321.0 |
| EIF2B3 | -2126.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| EIF2B1 | -1034.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| EIF4H | -577.0 |
| EIF4EBP1 | -355.0 |
| EIF3D | -226.0 |
| EIF2S1 | 150.0 |
| EIF4E | 207.0 |
| RPL27A | 228.0 |
| EIF4A1 | 285.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| EIF2B2 | 1189.0 |
| RPL30 | 1658.0 |
| EIF2B5 | 2648.0 |
| EIF1AX | 2870.0 |
| EIF4B | 2984.0 |
| RPS9 | 3205.0 |
| EIF4A2 | 3322.0 |
| EIF5 | 3324.0 |
| RPL12 | 3366.0 |
| EIF3C | 3490.5 |
| EIF2S3 | 3918.5 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
| EIF4G1 | 5853.0 |
| EIF3A | 6202.0 |
Eukaryotic Translation Initiation
| 345 | |
|---|---|
| set | Eukaryotic Translation Initiation |
| setSize | 96 |
| pANOVA | 1.41e-11 |
| s.dist | -0.399 |
| p.adjustANOVA | 9.73e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004 |
| RPS24 | -5953 |
| RPL38 | -5924 |
| RPL10A | -5900 |
| RPS15 | -5897 |
| EIF2S2 | -5891 |
| RPL29 | -5888 |
| EIF3F | -5822 |
| RPL23A | -5817 |
| RPS28 | -5799 |
| EIF3K | -5794 |
| RPS26 | -5788 |
| RPL15 | -5754 |
| UBA52 | -5753 |
| RPL32 | -5739 |
| RPL4 | -5689 |
| RPS25 | -5561 |
| RPS27L | -5448 |
| FAU | -5426 |
| RPL24 | -5413 |
| GeneID | Gene Rank |
|---|---|
| RPL35 | -6004.0 |
| RPS24 | -5953.0 |
| RPL38 | -5924.0 |
| RPL10A | -5900.0 |
| RPS15 | -5897.0 |
| EIF2S2 | -5891.0 |
| RPL29 | -5888.0 |
| EIF3F | -5822.0 |
| RPL23A | -5817.0 |
| RPS28 | -5799.0 |
| EIF3K | -5794.0 |
| RPS26 | -5788.0 |
| RPL15 | -5754.0 |
| UBA52 | -5753.0 |
| RPL32 | -5739.0 |
| RPL4 | -5689.0 |
| RPS25 | -5561.0 |
| RPS27L | -5448.0 |
| FAU | -5426.0 |
| RPL24 | -5413.0 |
| EIF5B | -5385.0 |
| RPS27A | -5344.0 |
| RPL34 | -5319.0 |
| RPS8 | -5264.0 |
| RPL5 | -5244.0 |
| EIF3H | -5175.0 |
| RPL35A | -5148.0 |
| RPL14 | -5046.0 |
| EIF3J | -5003.0 |
| RPS5 | -4988.0 |
| RPS17 | -4860.0 |
| EIF3I | -4701.0 |
| EIF3E | -4661.0 |
| RPS19 | -4560.0 |
| RPS11 | -4469.0 |
| EIF3L | -4434.0 |
| RPS20 | -4177.0 |
| RPS6 | -4095.0 |
| RPSA | -4075.5 |
| EIF3M | -3968.0 |
| RPL6 | -3955.0 |
| RPL36A | -3952.0 |
| RPLP0 | -3931.0 |
| RPL22 | -3911.0 |
| EIF3G | -3720.0 |
| EIF2B4 | -3530.0 |
| RPS18 | -3498.0 |
| RPS12 | -3380.0 |
| RPL37A | -3166.0 |
| RPS3 | -2876.0 |
| RPS23 | -2875.0 |
| RPS13 | -2855.0 |
| RPL7 | -2783.0 |
| EIF3B | -2321.0 |
| EIF2B3 | -2126.0 |
| RPL19 | -2039.0 |
| RPL28 | -2011.0 |
| RPS14 | -1992.0 |
| RPL13 | -1933.0 |
| RPL36 | -1905.0 |
| RPL23 | -1859.0 |
| RPS2 | -1741.0 |
| RPS29 | -1526.0 |
| RPLP2 | -1523.0 |
| EIF2B1 | -1034.0 |
| RPL3 | -953.0 |
| RPL11 | -812.0 |
| RPS10 | -810.0 |
| RPS21 | -782.0 |
| EIF4H | -577.0 |
| EIF4EBP1 | -355.0 |
| EIF3D | -226.0 |
| EIF2S1 | 150.0 |
| EIF4E | 207.0 |
| RPL27A | 228.0 |
| EIF4A1 | 285.0 |
| RPL8 | 395.0 |
| RPS3A | 729.0 |
| RPS16 | 922.0 |
| RPLP1 | 1114.0 |
| EIF2B2 | 1189.0 |
| RPL30 | 1658.0 |
| EIF2B5 | 2648.0 |
| EIF1AX | 2870.0 |
| EIF4B | 2984.0 |
| RPS9 | 3205.0 |
| EIF4A2 | 3322.0 |
| EIF5 | 3324.0 |
| RPL12 | 3366.0 |
| EIF3C | 3490.5 |
| EIF2S3 | 3918.5 |
| RPL10 | 3987.0 |
| RPS7 | 4000.0 |
| RPL27 | 4941.0 |
| EIF4G1 | 5853.0 |
| EIF3A | 6202.0 |
Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.2.1 (2022-06-23)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 20.04.4 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/openblas-pthread/libblas.so.3
## LAPACK: /usr/lib/x86_64-linux-gnu/openblas-pthread/liblapack.so.3
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## attached base packages:
## [1] stats4 stats graphics grDevices utils datasets methods
## [8] base
##
## other attached packages:
## [1] pkgload_1.3.0 GGally_2.1.2
## [3] ggplot2_3.3.6 beeswarm_0.4.0
## [5] gtools_3.9.2.2 tibble_3.1.7
## [7] echarts4r_0.4.4 RColorBrewer_1.1-3
## [9] kableExtra_1.3.4 biomaRt_2.52.0
## [11] dplyr_1.0.9 mitch_1.8.0
## [13] gplots_3.1.3 DESeq2_1.36.0
## [15] SummarizedExperiment_1.26.1 Biobase_2.56.0
## [17] MatrixGenerics_1.8.0 matrixStats_0.62.0
## [19] GenomicRanges_1.48.0 GenomeInfoDb_1.32.2
## [21] IRanges_2.30.0 S4Vectors_0.34.0
## [23] BiocGenerics_0.42.0 reshape2_1.4.4
##
## loaded via a namespace (and not attached):
## [1] colorspace_2.0-3 ellipsis_0.3.2 XVector_0.36.0
## [4] rstudioapi_0.13 bit64_4.0.5 AnnotationDbi_1.58.0
## [7] fansi_1.0.3 xml2_1.3.3 codetools_0.2-18
## [10] splines_4.2.1 cachem_1.0.6 geneplotter_1.74.0
## [13] knitr_1.39 jsonlite_1.8.0 annotate_1.74.0
## [16] dbplyr_2.2.1 png_0.1-7 shiny_1.7.1
## [19] compiler_4.2.1 httr_1.4.3 assertthat_0.2.1
## [22] Matrix_1.4-1 fastmap_1.1.0 cli_3.3.0
## [25] later_1.3.0 htmltools_0.5.2 prettyunits_1.1.1
## [28] tools_4.2.1 gtable_0.3.0 glue_1.6.2
## [31] GenomeInfoDbData_1.2.8 rappdirs_0.3.3 Rcpp_1.0.8.3
## [34] jquerylib_0.1.4 vctrs_0.4.1 Biostrings_2.64.0
## [37] svglite_2.1.0 xfun_0.31 stringr_1.4.0
## [40] rvest_1.0.2 mime_0.12 lifecycle_1.0.1
## [43] XML_3.99-0.10 zlibbioc_1.42.0 MASS_7.3-58
## [46] scales_1.2.0 hms_1.1.1 promises_1.2.0.1
## [49] parallel_4.2.1 yaml_2.3.5 curl_4.3.2
## [52] memoise_2.0.1 gridExtra_2.3 sass_0.4.1
## [55] reshape_0.8.9 stringi_1.7.6 RSQLite_2.2.14
## [58] highr_0.9 genefilter_1.78.0 caTools_1.18.2
## [61] filelock_1.0.2 BiocParallel_1.30.3 systemfonts_1.0.4
## [64] rlang_1.0.3 pkgconfig_2.0.3 bitops_1.0-7
## [67] evaluate_0.15 lattice_0.20-45 purrr_0.3.4
## [70] htmlwidgets_1.5.4 bit_4.0.4 tidyselect_1.1.2
## [73] plyr_1.8.7 magrittr_2.0.3 R6_2.5.1
## [76] generics_0.1.2 DelayedArray_0.22.0 DBI_1.1.3
## [79] withr_2.5.0 pillar_1.7.0 survival_3.4-0
## [82] KEGGREST_1.36.2 RCurl_1.98-1.7 crayon_1.5.1
## [85] KernSmooth_2.23-20 utf8_1.2.2 BiocFileCache_2.4.0
## [88] rmarkdown_2.14 progress_1.2.2 locfit_1.5-9.5
## [91] grid_4.2.1 blob_1.2.3 webshot_0.5.3
## [94] digest_0.6.29 xtable_1.8-4 httpuv_1.6.5
## [97] munsell_0.5.0 viridisLite_0.4.0 bslib_0.3.1
END of report