date generated: 2024-02-26
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 | |
|---|---|
| 5_8S_rRNA | -6.143587 |
| 7SK | -1.282326 |
| A1BG | -4.436253 |
| A1BG.AS1 | -1.588745 |
| A2M | 2.397394 |
| A2M.AS1 | 2.213143 |
Here are some metrics about the input data profile:
| Profile metrics | |
|---|---|
| num_genesets | 2612 |
| num_genes_in_profile | 16680 |
| duplicated_genes_present | 0 |
| num_profile_genes_in_sets | 8318 |
| num_profile_genes_not_in_sets | 8362 |
Here is a plot of the input profiles. Note the dynamic ranges.
Here is the contour plot of the profile including all detected genes.
Here are some metrics about the gene sets used:
GMT file of genesets: ReactomePathways_2023-09-01.gmt| Gene sets metrics | |
|---|---|
| num_genesets | 2612 |
| num_genesets_excluded | 1141 |
| num_genesets_included | 1471 |
Significance is calculated by -log10(p-value). All points shown are FDR<0.05.
Significance is calculated by -log10(p-value). Top N sets shown irrespective of FDR.
Top N= 50 gene sets
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| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | 13 | 1.56e-05 | -0.692 | 1.10e-04 |
| Formation of tubulin folding intermediates by CCT/TriC | 21 | 1.95e-07 | -0.656 | 2.09e-06 |
| Transport of connexons to the plasma membrane | 14 | 4.42e-05 | -0.630 | 2.94e-04 |
| Folding of actin by CCT/TriC | 10 | 8.71e-04 | -0.608 | 4.37e-03 |
| Prefoldin mediated transfer of substrate to CCT/TriC | 25 | 2.32e-07 | -0.597 | 2.40e-06 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 28 | 7.05e-08 | -0.588 | 8.37e-07 |
| Eukaryotic Translation Elongation | 92 | 6.24e-22 | -0.580 | 1.15e-19 |
| Josephin domain DUBs | 10 | 1.69e-03 | -0.573 | 7.89e-03 |
| Peptide chain elongation | 87 | 2.25e-20 | -0.573 | 1.84e-18 |
| TP53 Regulates Transcription of Death Receptors and Ligands | 10 | 1.84e-03 | -0.569 | 8.53e-03 |
| Gluconeogenesis | 27 | 3.56e-07 | -0.566 | 3.44e-06 |
| Viral mRNA Translation | 87 | 7.33e-20 | -0.565 | 5.00e-18 |
| Erythrocytes take up carbon dioxide and release oxygen | 10 | 2.01e-03 | -0.564 | 9.13e-03 |
| O2/CO2 exchange in erythrocytes | 10 | 2.01e-03 | -0.564 | 9.13e-03 |
| Keratan sulfate biosynthesis | 26 | 6.42e-07 | -0.564 | 6.02e-06 |
| Eukaryotic Translation Termination | 91 | 7.47e-20 | -0.553 | 5.00e-18 |
| STAT3 nuclear events downstream of ALK signaling | 10 | 2.81e-03 | -0.546 | 1.22e-02 |
| SARS-CoV-1 modulates host translation machinery | 36 | 1.45e-08 | -0.546 | 2.00e-07 |
| Formation of a pool of free 40S subunits | 99 | 1.09e-20 | -0.542 | 1.12e-18 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 93 | 2.33e-19 | -0.539 | 1.49e-17 |
| Syndecan interactions | 26 | 2.00e-06 | -0.539 | 1.61e-05 |
| SRP-dependent cotranslational protein targeting to membrane | 110 | 4.00e-22 | -0.533 | 8.41e-20 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 12 | 1.47e-03 | 0.530 | 6.91e-03 |
| Selenocysteine synthesis | 91 | 2.70e-18 | -0.529 | 1.47e-16 |
| Suppression of phagosomal maturation | 13 | 9.79e-04 | -0.528 | 4.87e-03 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 109 | 1.67e-21 | -0.528 | 2.05e-19 |
| Chondroitin sulfate biosynthesis | 16 | 2.93e-04 | -0.523 | 1.64e-03 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 110 | 4.06e-21 | -0.520 | 4.60e-19 |
| Activation of Matrix Metalloproteinases | 23 | 1.61e-05 | -0.520 | 1.13e-04 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 99 | 6.14e-19 | -0.517 | 3.48e-17 |
| Keratan sulfate degradation | 13 | 1.31e-03 | -0.515 | 6.34e-03 |
| Crosslinking of collagen fibrils | 14 | 9.02e-04 | -0.512 | 4.50e-03 |
| Cap-dependent Translation Initiation | 117 | 1.19e-21 | -0.511 | 1.59e-19 |
| Eukaryotic Translation Initiation | 117 | 1.19e-21 | -0.511 | 1.59e-19 |
| ATF6 (ATF6-alpha) activates chaperones | 12 | 2.23e-03 | -0.510 | 1.00e-02 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | 70 | 1.95e-13 | -0.508 | 6.66e-12 |
| Formation of ATP by chemiosmotic coupling | 16 | 5.09e-04 | -0.502 | 2.69e-03 |
| Ubiquitin-dependent degradation of Cyclin D | 50 | 1.02e-09 | -0.499 | 2.06e-08 |
| Formation of the ternary complex, and subsequently, the 43S complex | 51 | 7.02e-10 | -0.499 | 1.50e-08 |
| Selenoamino acid metabolism | 113 | 6.11e-20 | -0.498 | 4.49e-18 |
| Diseases associated with glycosaminoglycan metabolism | 38 | 1.11e-07 | -0.497 | 1.26e-06 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 10 | 6.60e-03 | -0.496 | 2.55e-02 |
| FGFR2 ligand binding and activation | 10 | 6.97e-03 | -0.493 | 2.67e-02 |
| Downregulation of ERBB2:ERBB3 signaling | 13 | 2.11e-03 | -0.492 | 9.55e-03 |
| Response of EIF2AK1 (HRI) to heme deficiency | 14 | 1.44e-03 | -0.492 | 6.87e-03 |
| Membrane binding and targetting of GAG proteins | 14 | 1.45e-03 | -0.491 | 6.87e-03 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 14 | 1.45e-03 | -0.491 | 6.87e-03 |
| Keratan sulfate/keratin metabolism | 32 | 1.58e-06 | -0.490 | 1.30e-05 |
| Diseases associated with glycosylation precursor biosynthesis | 15 | 1.02e-03 | -0.490 | 5.03e-03 |
| Regulation of RUNX3 expression and activity | 55 | 4.18e-10 | -0.487 | 9.45e-09 |
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | 13 | 1.56e-05 | -0.692000 | 1.10e-04 |
| Formation of tubulin folding intermediates by CCT/TriC | 21 | 1.95e-07 | -0.656000 | 2.09e-06 |
| Transport of connexons to the plasma membrane | 14 | 4.42e-05 | -0.630000 | 2.94e-04 |
| Folding of actin by CCT/TriC | 10 | 8.71e-04 | -0.608000 | 4.37e-03 |
| Prefoldin mediated transfer of substrate to CCT/TriC | 25 | 2.32e-07 | -0.597000 | 2.40e-06 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 28 | 7.05e-08 | -0.588000 | 8.37e-07 |
| Eukaryotic Translation Elongation | 92 | 6.24e-22 | -0.580000 | 1.15e-19 |
| Josephin domain DUBs | 10 | 1.69e-03 | -0.573000 | 7.89e-03 |
| Peptide chain elongation | 87 | 2.25e-20 | -0.573000 | 1.84e-18 |
| TP53 Regulates Transcription of Death Receptors and Ligands | 10 | 1.84e-03 | -0.569000 | 8.53e-03 |
| Gluconeogenesis | 27 | 3.56e-07 | -0.566000 | 3.44e-06 |
| Viral mRNA Translation | 87 | 7.33e-20 | -0.565000 | 5.00e-18 |
| Erythrocytes take up carbon dioxide and release oxygen | 10 | 2.01e-03 | -0.564000 | 9.13e-03 |
| O2/CO2 exchange in erythrocytes | 10 | 2.01e-03 | -0.564000 | 9.13e-03 |
| Keratan sulfate biosynthesis | 26 | 6.42e-07 | -0.564000 | 6.02e-06 |
| Eukaryotic Translation Termination | 91 | 7.47e-20 | -0.553000 | 5.00e-18 |
| STAT3 nuclear events downstream of ALK signaling | 10 | 2.81e-03 | -0.546000 | 1.22e-02 |
| SARS-CoV-1 modulates host translation machinery | 36 | 1.45e-08 | -0.546000 | 2.00e-07 |
| Formation of a pool of free 40S subunits | 99 | 1.09e-20 | -0.542000 | 1.12e-18 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 93 | 2.33e-19 | -0.539000 | 1.49e-17 |
| Syndecan interactions | 26 | 2.00e-06 | -0.539000 | 1.61e-05 |
| SRP-dependent cotranslational protein targeting to membrane | 110 | 4.00e-22 | -0.533000 | 8.41e-20 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 12 | 1.47e-03 | 0.530000 | 6.91e-03 |
| Selenocysteine synthesis | 91 | 2.70e-18 | -0.529000 | 1.47e-16 |
| Suppression of phagosomal maturation | 13 | 9.79e-04 | -0.528000 | 4.87e-03 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 109 | 1.67e-21 | -0.528000 | 2.05e-19 |
| Chondroitin sulfate biosynthesis | 16 | 2.93e-04 | -0.523000 | 1.64e-03 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 110 | 4.06e-21 | -0.520000 | 4.60e-19 |
| Activation of Matrix Metalloproteinases | 23 | 1.61e-05 | -0.520000 | 1.13e-04 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 99 | 6.14e-19 | -0.517000 | 3.48e-17 |
| Keratan sulfate degradation | 13 | 1.31e-03 | -0.515000 | 6.34e-03 |
| Crosslinking of collagen fibrils | 14 | 9.02e-04 | -0.512000 | 4.50e-03 |
| Cap-dependent Translation Initiation | 117 | 1.19e-21 | -0.511000 | 1.59e-19 |
| Eukaryotic Translation Initiation | 117 | 1.19e-21 | -0.511000 | 1.59e-19 |
| ATF6 (ATF6-alpha) activates chaperones | 12 | 2.23e-03 | -0.510000 | 1.00e-02 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | 70 | 1.95e-13 | -0.508000 | 6.66e-12 |
| Formation of ATP by chemiosmotic coupling | 16 | 5.09e-04 | -0.502000 | 2.69e-03 |
| Ubiquitin-dependent degradation of Cyclin D | 50 | 1.02e-09 | -0.499000 | 2.06e-08 |
| Formation of the ternary complex, and subsequently, the 43S complex | 51 | 7.02e-10 | -0.499000 | 1.50e-08 |
| Selenoamino acid metabolism | 113 | 6.11e-20 | -0.498000 | 4.49e-18 |
| Diseases associated with glycosaminoglycan metabolism | 38 | 1.11e-07 | -0.497000 | 1.26e-06 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 10 | 6.60e-03 | -0.496000 | 2.55e-02 |
| FGFR2 ligand binding and activation | 10 | 6.97e-03 | -0.493000 | 2.67e-02 |
| Downregulation of ERBB2:ERBB3 signaling | 13 | 2.11e-03 | -0.492000 | 9.55e-03 |
| Response of EIF2AK1 (HRI) to heme deficiency | 14 | 1.44e-03 | -0.492000 | 6.87e-03 |
| Membrane binding and targetting of GAG proteins | 14 | 1.45e-03 | -0.491000 | 6.87e-03 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 14 | 1.45e-03 | -0.491000 | 6.87e-03 |
| Keratan sulfate/keratin metabolism | 32 | 1.58e-06 | -0.490000 | 1.30e-05 |
| Diseases associated with glycosylation precursor biosynthesis | 15 | 1.02e-03 | -0.490000 | 5.03e-03 |
| Regulation of RUNX3 expression and activity | 55 | 4.18e-10 | -0.487000 | 9.45e-09 |
| IRE1alpha activates chaperones | 49 | 4.10e-09 | -0.485000 | 7.05e-08 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 59 | 1.30e-10 | -0.484000 | 3.35e-09 |
| Regulation of ornithine decarboxylase (ODC) | 48 | 8.75e-09 | -0.480000 | 1.29e-07 |
| Ribosomal scanning and start codon recognition | 58 | 2.71e-10 | -0.479000 | 6.54e-09 |
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 49 | 6.74e-09 | -0.479000 | 1.05e-07 |
| p53-Independent DNA Damage Response | 49 | 6.74e-09 | -0.479000 | 1.05e-07 |
| p53-Independent G1/S DNA damage checkpoint | 49 | 6.74e-09 | -0.479000 | 1.05e-07 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 48 | 1.08e-08 | -0.477000 | 1.57e-07 |
| Translation initiation complex formation | 58 | 3.39e-10 | -0.477000 | 8.04e-09 |
| XBP1(S) activates chaperone genes | 47 | 1.64e-08 | -0.476000 | 2.19e-07 |
| ATF6 (ATF6-alpha) activates chaperone genes | 10 | 9.22e-03 | -0.476000 | 3.42e-02 |
| Hh mutants are degraded by ERAD | 53 | 2.16e-09 | -0.475000 | 3.93e-08 |
| Autodegradation of the E3 ubiquitin ligase COP1 | 49 | 1.14e-08 | -0.471000 | 1.64e-07 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 53 | 3.30e-09 | -0.470000 | 5.84e-08 |
| Transferrin endocytosis and recycling | 28 | 1.78e-05 | -0.469000 | 1.23e-04 |
| Insulin receptor recycling | 26 | 3.85e-05 | -0.466000 | 2.59e-04 |
| Degradation of DVL | 55 | 2.22e-09 | -0.466000 | 3.98e-08 |
| Glycogen synthesis | 12 | 5.28e-03 | -0.465000 | 2.08e-02 |
| Assembly Of The HIV Virion | 16 | 1.32e-03 | -0.464000 | 6.39e-03 |
| Vif-mediated degradation of APOBEC3G | 52 | 7.69e-09 | -0.463000 | 1.17e-07 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 113 | 2.19e-17 | -0.462000 | 1.07e-15 |
| Nonsense-Mediated Decay (NMD) | 113 | 2.19e-17 | -0.462000 | 1.07e-15 |
| Negative regulation of NOTCH4 signaling | 54 | 5.18e-09 | -0.459000 | 8.65e-08 |
| Defective CFTR causes cystic fibrosis | 59 | 1.09e-09 | -0.459000 | 2.12e-08 |
| Collagen biosynthesis and modifying enzymes | 60 | 8.18e-10 | -0.458000 | 1.69e-08 |
| Hh mutants abrogate ligand secretion | 55 | 4.17e-09 | -0.458000 | 7.05e-08 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 53 | 8.32e-09 | -0.457000 | 1.24e-07 |
| Vpu mediated degradation of CD4 | 50 | 2.57e-08 | -0.455000 | 3.32e-07 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 52 | 1.41e-08 | -0.455000 | 1.96e-07 |
| Metabolism of polyamines | 56 | 4.17e-09 | -0.454000 | 7.05e-08 |
| Scavenging of heme from plasma | 13 | 4.79e-03 | -0.452000 | 1.91e-02 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 64 | 4.10e-10 | -0.452000 | 9.45e-09 |
| Antimicrobial peptides | 26 | 6.78e-05 | -0.451000 | 4.41e-04 |
| SHC-mediated cascade:FGFR3 | 12 | 6.83e-03 | -0.451000 | 2.63e-02 |
| SCF-beta-TrCP mediated degradation of Emi1 | 53 | 1.38e-08 | -0.451000 | 1.93e-07 |
| Dectin-1 mediated noncanonical NF-kB signaling | 58 | 3.36e-09 | -0.449000 | 5.88e-08 |
| Defective Intrinsic Pathway for Apoptosis | 21 | 3.75e-04 | -0.448000 | 2.03e-03 |
| Chemokine receptors bind chemokines | 36 | 3.28e-06 | -0.448000 | 2.57e-05 |
| Cross-presentation of soluble exogenous antigens (endosomes) | 46 | 1.55e-07 | -0.447000 | 1.69e-06 |
| The canonical retinoid cycle in rods (twilight vision) | 11 | 1.05e-02 | 0.445000 | 3.83e-02 |
| Post-chaperonin tubulin folding pathway | 18 | 1.10e-03 | -0.444000 | 5.44e-03 |
| Collagen degradation | 54 | 1.66e-08 | -0.444000 | 2.20e-07 |
| Zinc transporters | 10 | 1.51e-02 | -0.444000 | 5.22e-02 |
| NIK–>noncanonical NF-kB signaling | 57 | 7.47e-09 | -0.443000 | 1.14e-07 |
| Cristae formation | 29 | 3.94e-05 | -0.441000 | 2.64e-04 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 22 | 3.47e-04 | -0.441000 | 1.91e-03 |
| Stabilization of p53 | 54 | 2.48e-08 | -0.439000 | 3.23e-07 |
| Regulation of expression of SLITs and ROBOs | 162 | 9.58e-22 | -0.436000 | 1.57e-19 |
| GLI3 is processed to GLI3R by the proteasome | 57 | 1.38e-08 | -0.435000 | 1.93e-07 |
| Regulation of Apoptosis | 51 | 8.75e-08 | -0.433000 | 1.01e-06 |
| DARPP-32 events | 22 | 4.62e-04 | -0.431000 | 2.45e-03 |
| FGFR2 mutant receptor activation | 24 | 2.89e-04 | -0.428000 | 1.62e-03 |
| Regulation of BACH1 activity | 11 | 1.42e-02 | -0.427000 | 4.98e-02 |
| SCF(Skp2)-mediated degradation of p27/p21 | 59 | 1.50e-08 | -0.426000 | 2.04e-07 |
| NF-kB is activated and signals survival | 13 | 7.81e-03 | -0.426000 | 2.95e-02 |
| Degradation of GLI2 by the proteasome | 57 | 2.69e-08 | -0.426000 | 3.44e-07 |
| Cytosolic tRNA aminoacylation | 24 | 3.15e-04 | -0.425000 | 1.75e-03 |
| Cellular response to starvation | 149 | 4.98e-19 | -0.423000 | 2.93e-17 |
| Regulation of RUNX2 expression and activity | 70 | 9.61e-10 | -0.423000 | 1.96e-08 |
| Metabolism of Angiotensinogen to Angiotensins | 13 | 8.34e-03 | -0.423000 | 3.13e-02 |
| Hedgehog ligand biogenesis | 60 | 1.56e-08 | -0.422000 | 2.10e-07 |
| Collagen chain trimerization | 38 | 7.11e-06 | -0.421000 | 5.28e-05 |
| Gap junction assembly | 21 | 8.74e-04 | -0.420000 | 4.37e-03 |
| Activation of NF-kappaB in B cells | 65 | 5.77e-09 | -0.418000 | 9.54e-08 |
| Beta-catenin phosphorylation cascade | 17 | 2.97e-03 | -0.416000 | 1.29e-02 |
| SHC-mediated cascade:FGFR4 | 11 | 1.69e-02 | -0.416000 | 5.74e-02 |
| Downstream TCR signaling | 82 | 8.24e-11 | -0.415000 | 2.20e-09 |
| Nuclear events mediated by NFE2L2 | 76 | 4.13e-10 | -0.415000 | 9.45e-09 |
| Degradation of GLI1 by the proteasome | 57 | 6.85e-08 | -0.413000 | 8.32e-07 |
| Cellular response to hypoxia | 72 | 1.43e-09 | -0.413000 | 2.69e-08 |
| Interleukin-10 signaling | 35 | 2.41e-05 | -0.412000 | 1.65e-04 |
| Pentose phosphate pathway | 13 | 1.00e-02 | -0.412000 | 3.69e-02 |
| Signaling by FGFR2 IIIa TM | 19 | 1.93e-03 | -0.411000 | 8.89e-03 |
| PD-1 signaling | 11 | 1.85e-02 | -0.410000 | 6.19e-02 |
| SUMOylation of immune response proteins | 11 | 1.86e-02 | -0.410000 | 6.22e-02 |
| Assembly of collagen fibrils and other multimeric structures | 54 | 2.06e-07 | -0.409000 | 2.17e-06 |
| Degradation of beta-catenin by the destruction complex | 83 | 1.26e-10 | -0.408000 | 3.32e-09 |
| Asymmetric localization of PCP proteins | 61 | 3.65e-08 | -0.408000 | 4.59e-07 |
| Collagen formation | 81 | 2.31e-10 | -0.407000 | 5.68e-09 |
| Striated Muscle Contraction | 30 | 1.14e-04 | -0.407000 | 7.04e-04 |
| SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 11 | 1.94e-02 | -0.407000 | 6.46e-02 |
| TICAM1-dependent activation of IRF3/IRF7 | 12 | 1.48e-02 | -0.406000 | 5.13e-02 |
| Degradation of AXIN | 53 | 3.16e-07 | -0.406000 | 3.10e-06 |
| Translation | 291 | 1.19e-32 | -0.405000 | 4.39e-30 |
| COPI-mediated anterograde transport | 92 | 1.85e-11 | -0.405000 | 5.22e-10 |
| SARS-CoV-2 modulates host translation machinery | 49 | 1.12e-06 | -0.402000 | 9.49e-06 |
| SHC-mediated cascade:FGFR2 | 14 | 9.41e-03 | -0.401000 | 3.49e-02 |
| RUNX3 regulates p14-ARF | 10 | 2.92e-02 | -0.398000 | 9.01e-02 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models | 18 | 3.47e-03 | -0.398000 | 1.45e-02 |
| Neurodegenerative Diseases | 18 | 3.47e-03 | -0.398000 | 1.45e-02 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | 24 | 7.43e-04 | -0.398000 | 3.82e-03 |
| Pausing and recovery of Tat-mediated HIV elongation | 30 | 1.67e-04 | -0.397000 | 9.89e-04 |
| Tat-mediated HIV elongation arrest and recovery | 30 | 1.67e-04 | -0.397000 | 9.89e-04 |
| Interconversion of nucleotide di- and triphosphates | 27 | 3.57e-04 | -0.397000 | 1.94e-03 |
| p53-Dependent G1 DNA Damage Response | 62 | 7.04e-08 | -0.396000 | 8.37e-07 |
| p53-Dependent G1/S DNA damage checkpoint | 62 | 7.04e-08 | -0.396000 | 8.37e-07 |
| Cargo concentration in the ER | 28 | 3.13e-04 | -0.394000 | 1.75e-03 |
| SLBP independent Processing of Histone Pre-mRNAs | 10 | 3.14e-02 | -0.393000 | 9.53e-02 |
| Unwinding of DNA | 11 | 2.47e-02 | -0.391000 | 7.79e-02 |
| Orc1 removal from chromatin | 67 | 3.58e-08 | -0.389000 | 4.54e-07 |
| KEAP1-NFE2L2 pathway | 101 | 1.48e-11 | -0.389000 | 4.27e-10 |
| Assembly of active LPL and LIPC lipase complexes | 12 | 1.98e-02 | -0.389000 | 6.50e-02 |
| Regulation of NPAS4 gene expression | 12 | 2.01e-02 | 0.388000 | 6.56e-02 |
| G1/S DNA Damage Checkpoints | 63 | 1.06e-07 | -0.387000 | 1.21e-06 |
| Unfolded Protein Response (UPR) | 91 | 2.15e-10 | -0.385000 | 5.37e-09 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 69 | 3.85e-08 | -0.383000 | 4.79e-07 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | 11 | 2.86e-02 | -0.381000 | 8.87e-02 |
| Anchoring fibril formation | 11 | 2.88e-02 | -0.381000 | 8.92e-02 |
| Mitochondrial protein import | 63 | 2.00e-07 | -0.379000 | 2.12e-06 |
| N-Glycan antennae elongation | 13 | 1.85e-02 | -0.377000 | 6.19e-02 |
| Somitogenesis | 50 | 4.38e-06 | -0.375000 | 3.34e-05 |
| Assembly and cell surface presentation of NMDA receptors | 34 | 1.54e-04 | -0.375000 | 9.32e-04 |
| Phosphorylation of CD3 and TCR zeta chains | 11 | 3.13e-02 | -0.375000 | 9.53e-02 |
| TNFR2 non-canonical NF-kB pathway | 87 | 1.57e-09 | -0.374000 | 2.92e-08 |
| Regulation of PTEN stability and activity | 67 | 1.17e-07 | -0.374000 | 1.31e-06 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 87 | 1.63e-09 | -0.374000 | 3.00e-08 |
| The activation of arylsulfatases | 10 | 4.05e-02 | -0.374000 | 1.15e-01 |
| Interleukin-4 and Interleukin-13 signaling | 90 | 1.04e-09 | -0.372000 | 2.07e-08 |
| FCERI mediated NF-kB activation | 81 | 7.10e-09 | -0.372000 | 1.10e-07 |
| Influenza Viral RNA Transcription and Replication | 134 | 1.05e-13 | -0.372000 | 3.78e-12 |
| APC/C:Cdc20 mediated degradation of Securin | 66 | 1.75e-07 | -0.372000 | 1.89e-06 |
| Post-translational protein phosphorylation | 78 | 1.37e-08 | -0.372000 | 1.93e-07 |
| Autodegradation of Cdh1 by Cdh1:APC/C | 64 | 3.15e-07 | -0.370000 | 3.10e-06 |
| Transcriptional regulation by RUNX3 | 94 | 6.11e-10 | -0.369000 | 1.32e-08 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | 23 | 2.27e-03 | -0.368000 | 1.02e-02 |
| Signaling by ROBO receptors | 201 | 2.82e-19 | -0.367000 | 1.73e-17 |
| Regulation of TP53 Activity through Association with Co-factors | 10 | 4.46e-02 | -0.367000 | 1.21e-01 |
| Degradation of cysteine and homocysteine | 12 | 2.78e-02 | -0.367000 | 8.66e-02 |
| Aggrephagy | 35 | 1.91e-04 | -0.364000 | 1.12e-03 |
| MASTL Facilitates Mitotic Progression | 10 | 4.61e-02 | -0.364000 | 1.24e-01 |
| Iron uptake and transport | 55 | 3.32e-06 | -0.363000 | 2.58e-05 |
| COPI-dependent Golgi-to-ER retrograde traffic | 86 | 6.50e-09 | -0.362000 | 1.05e-07 |
| ER to Golgi Anterograde Transport | 141 | 1.26e-13 | -0.362000 | 4.42e-12 |
| Transcriptional regulation by RUNX2 | 114 | 2.65e-11 | -0.361000 | 7.23e-10 |
| PINK1-PRKN Mediated Mitophagy | 21 | 4.19e-03 | -0.361000 | 1.71e-02 |
| HSF1 activation | 25 | 1.80e-03 | -0.361000 | 8.37e-03 |
| Common Pathway of Fibrin Clot Formation | 10 | 4.91e-02 | -0.359000 | 1.31e-01 |
| Chondroitin sulfate/dermatan sulfate metabolism | 45 | 3.09e-05 | -0.359000 | 2.09e-04 |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 11 | 3.93e-02 | -0.359000 | 1.12e-01 |
| ABC transporter disorders | 69 | 2.75e-07 | -0.358000 | 2.75e-06 |
| p75NTR signals via NF-kB | 16 | 1.33e-02 | -0.358000 | 4.72e-02 |
| RHO GTPases activate IQGAPs | 24 | 2.47e-03 | -0.357000 | 1.09e-02 |
| Complex I biogenesis | 51 | 1.09e-05 | -0.356000 | 7.84e-05 |
| Response of Mtb to phagocytosis | 23 | 3.22e-03 | -0.355000 | 1.36e-02 |
| Interleukin-2 signaling | 11 | 4.16e-02 | -0.355000 | 1.17e-01 |
| Negative regulation of FGFR3 signaling | 23 | 3.27e-03 | -0.354000 | 1.37e-02 |
| Integrin cell surface interactions | 73 | 1.99e-07 | -0.352000 | 2.12e-06 |
| Packaging Of Telomere Ends | 12 | 3.59e-02 | -0.350000 | 1.06e-01 |
| Respiratory electron transport | 93 | 5.96e-09 | -0.349000 | 9.75e-08 |
| TCR signaling | 102 | 1.22e-09 | -0.348000 | 2.33e-08 |
| Dectin-2 family | 14 | 2.44e-02 | 0.347000 | 7.71e-02 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 72 | 3.46e-07 | -0.347000 | 3.37e-06 |
| Mitochondrial iron-sulfur cluster biogenesis | 13 | 3.06e-02 | -0.346000 | 9.34e-02 |
| CTNNB1 S33 mutants aren’t phosphorylated | 15 | 2.05e-02 | -0.346000 | 6.60e-02 |
| CTNNB1 S37 mutants aren’t phosphorylated | 15 | 2.05e-02 | -0.346000 | 6.60e-02 |
| CTNNB1 S45 mutants aren’t phosphorylated | 15 | 2.05e-02 | -0.346000 | 6.60e-02 |
| CTNNB1 T41 mutants aren’t phosphorylated | 15 | 2.05e-02 | -0.346000 | 6.60e-02 |
| Signaling by CTNNB1 phospho-site mutants | 15 | 2.05e-02 | -0.346000 | 6.60e-02 |
| Signaling by GSK3beta mutants | 15 | 2.05e-02 | -0.346000 | 6.60e-02 |
| Cohesin Loading onto Chromatin | 10 | 5.84e-02 | 0.346000 | 1.47e-01 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 17 | 1.37e-02 | -0.345000 | 4.84e-02 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 17 | 1.37e-02 | -0.345000 | 4.84e-02 |
| Downstream signaling events of B Cell Receptor (BCR) | 78 | 1.34e-07 | -0.345000 | 1.50e-06 |
| Major pathway of rRNA processing in the nucleolus and cytosol | 179 | 1.65e-15 | -0.345000 | 6.57e-14 |
| Maturation of spike protein 9694548 | 37 | 2.84e-04 | -0.345000 | 1.60e-03 |
| IL-6-type cytokine receptor ligand interactions | 13 | 3.14e-02 | -0.345000 | 9.54e-02 |
| Free fatty acids regulate insulin secretion | 10 | 5.95e-02 | 0.344000 | 1.48e-01 |
| Caspase-mediated cleavage of cytoskeletal proteins | 12 | 3.90e-02 | 0.344000 | 1.11e-01 |
| Metal ion SLC transporters | 18 | 1.19e-02 | -0.342000 | 4.29e-02 |
| HIV elongation arrest and recovery | 32 | 8.14e-04 | -0.342000 | 4.11e-03 |
| Pausing and recovery of HIV elongation | 32 | 8.14e-04 | -0.342000 | 4.11e-03 |
| Signaling by ALK | 27 | 2.12e-03 | -0.342000 | 9.55e-03 |
| CS/DS degradation | 11 | 4.97e-02 | -0.342000 | 1.31e-01 |
| Interleukin-1 signaling | 109 | 7.85e-10 | -0.341000 | 1.65e-08 |
| Attenuation phase | 22 | 5.75e-03 | -0.340000 | 2.24e-02 |
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 113 | 4.44e-10 | -0.340000 | 9.89e-09 |
| rRNA processing in the nucleus and cytosol | 189 | 8.24e-16 | -0.340000 | 3.37e-14 |
| E3 ubiquitin ligases ubiquitinate target proteins | 43 | 1.18e-04 | -0.339000 | 7.23e-04 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | 72 | 6.67e-07 | -0.339000 | 6.12e-06 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 73 | 5.70e-07 | -0.339000 | 5.37e-06 |
| Mitophagy | 28 | 1.94e-03 | -0.338000 | 8.90e-03 |
| CDK-mediated phosphorylation and removal of Cdc6 | 70 | 1.00e-06 | -0.338000 | 8.55e-06 |
| Mitochondrial translation elongation | 88 | 4.24e-08 | -0.338000 | 5.24e-07 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 27 | 2.47e-03 | -0.337000 | 1.09e-02 |
| Acetylcholine Neurotransmitter Release Cycle | 13 | 3.57e-02 | -0.336000 | 1.05e-01 |
| Serotonin Neurotransmitter Release Cycle | 15 | 2.41e-02 | -0.336000 | 7.65e-02 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | 49 | 4.73e-05 | -0.336000 | 3.13e-04 |
| Influenza Infection | 153 | 8.23e-13 | -0.335000 | 2.58e-11 |
| Interleukin-6 family signaling | 20 | 9.54e-03 | -0.335000 | 3.52e-02 |
| P2Y receptors | 11 | 5.45e-02 | 0.335000 | 1.40e-01 |
| Inactivation of CSF3 (G-CSF) signaling | 24 | 4.54e-03 | -0.335000 | 1.83e-02 |
| Negative regulation of FGFR2 signaling | 25 | 3.85e-03 | -0.334000 | 1.58e-02 |
| Glycogen storage diseases | 13 | 3.72e-02 | -0.334000 | 1.07e-01 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 70 | 1.40e-06 | -0.334000 | 1.17e-05 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 70 | 1.40e-06 | -0.334000 | 1.17e-05 |
| Regulation of RAS by GAPs | 65 | 3.58e-06 | -0.332000 | 2.75e-05 |
| Negative regulation of FGFR4 signaling | 22 | 6.97e-03 | -0.332000 | 2.67e-02 |
| Cyclin E associated events during G1/S transition | 81 | 2.58e-07 | -0.331000 | 2.60e-06 |
| Dopamine Neurotransmitter Release Cycle | 20 | 1.04e-02 | -0.331000 | 3.80e-02 |
| Assembly of the pre-replicative complex | 88 | 8.14e-08 | -0.331000 | 9.50e-07 |
| Budding and maturation of HIV virion | 27 | 3.08e-03 | -0.329000 | 1.32e-02 |
| Inhibition of DNA recombination at telomere | 26 | 3.71e-03 | -0.329000 | 1.54e-02 |
| Transport to the Golgi and subsequent modification | 166 | 2.82e-13 | -0.329000 | 9.43e-12 |
| NGF-stimulated transcription | 35 | 8.10e-04 | -0.327000 | 4.11e-03 |
| rRNA processing | 199 | 2.31e-15 | -0.326000 | 8.93e-14 |
| Lewis blood group biosynthesis | 10 | 7.53e-02 | -0.325000 | 1.78e-01 |
| Long-term potentiation | 19 | 1.45e-02 | -0.324000 | 5.03e-02 |
| Mitochondrial translation termination | 88 | 1.51e-07 | -0.324000 | 1.66e-06 |
| COPII-mediated vesicle transport | 63 | 9.06e-06 | -0.323000 | 6.57e-05 |
| Gamma carboxylation, hypusine formation and arylsulfatase activation | 33 | 1.35e-03 | -0.322000 | 6.49e-03 |
| Cyclin A:Cdk2-associated events at S phase entry | 83 | 3.90e-07 | -0.322000 | 3.75e-06 |
| AKT phosphorylates targets in the cytosol | 14 | 3.70e-02 | -0.322000 | 1.07e-01 |
| Regulation of APC/C activators between G1/S and early anaphase | 78 | 9.68e-07 | -0.321000 | 8.33e-06 |
| PCP/CE pathway | 87 | 2.44e-07 | -0.320000 | 2.51e-06 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 13 | 4.60e-02 | -0.320000 | 1.24e-01 |
| Elastic fibre formation | 40 | 4.93e-04 | -0.318000 | 2.61e-03 |
| Mitochondrial translation initiation | 88 | 2.53e-07 | -0.318000 | 2.57e-06 |
| Translation of Structural Proteins 9683701 | 29 | 3.09e-03 | -0.318000 | 1.32e-02 |
| Pyrimidine salvage | 10 | 8.32e-02 | -0.316000 | 1.92e-01 |
| ROS and RNS production in phagocytes | 31 | 2.33e-03 | -0.316000 | 1.04e-02 |
| N-glycan antennae elongation in the medial/trans-Golgi | 20 | 1.45e-02 | -0.316000 | 5.05e-02 |
| Hedgehog ‘on’ state | 82 | 8.60e-07 | -0.314000 | 7.57e-06 |
| Processing and activation of SUMO | 10 | 8.58e-02 | -0.314000 | 1.97e-01 |
| Infection with Mycobacterium tuberculosis | 27 | 5.02e-03 | -0.312000 | 1.98e-02 |
| TCF dependent signaling in response to WNT | 160 | 1.00e-11 | -0.312000 | 2.95e-10 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 30 | 3.13e-03 | -0.312000 | 1.33e-02 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | 30 | 3.18e-03 | -0.311000 | 1.34e-02 |
| Protein ubiquitination | 63 | 2.01e-05 | -0.311000 | 1.38e-04 |
| Lysine catabolism | 11 | 7.51e-02 | 0.310000 | 1.78e-01 |
| Norepinephrine Neurotransmitter Release Cycle | 15 | 3.79e-02 | -0.310000 | 1.09e-01 |
| CTLA4 inhibitory signaling | 19 | 1.96e-02 | -0.309000 | 6.47e-02 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 15 | 3.90e-02 | -0.308000 | 1.11e-01 |
| A tetrasaccharide linker sequence is required for GAG synthesis | 22 | 1.24e-02 | -0.308000 | 4.44e-02 |
| Phase 4 - resting membrane potential | 12 | 6.52e-02 | -0.307000 | 1.59e-01 |
| CLEC7A (Dectin-1) signaling | 95 | 2.26e-07 | -0.307000 | 2.36e-06 |
| Golgi-to-ER retrograde transport | 119 | 7.81e-09 | -0.306000 | 1.17e-07 |
| Switching of origins to a post-replicative state | 88 | 6.81e-07 | -0.306000 | 6.18e-06 |
| ABC transporters in lipid homeostasis | 12 | 6.71e-02 | 0.305000 | 1.63e-01 |
| TP53 Regulates Transcription of Caspase Activators and Caspases | 10 | 9.63e-02 | 0.304000 | 2.15e-01 |
| Calnexin/calreticulin cycle | 26 | 7.47e-03 | -0.303000 | 2.84e-02 |
| APC truncation mutants have impaired AXIN binding | 14 | 4.97e-02 | -0.303000 | 1.31e-01 |
| AXIN missense mutants destabilize the destruction complex | 14 | 4.97e-02 | -0.303000 | 1.31e-01 |
| Signaling by AMER1 mutants | 14 | 4.97e-02 | -0.303000 | 1.31e-01 |
| Signaling by APC mutants | 14 | 4.97e-02 | -0.303000 | 1.31e-01 |
| Signaling by AXIN mutants | 14 | 4.97e-02 | -0.303000 | 1.31e-01 |
| Truncations of AMER1 destabilize the destruction complex | 14 | 4.97e-02 | -0.303000 | 1.31e-01 |
| Interleukin-7 signaling | 19 | 2.22e-02 | -0.303000 | 7.10e-02 |
| Activation of AMPK downstream of NMDARs | 21 | 1.64e-02 | -0.303000 | 5.63e-02 |
| HSF1-dependent transactivation | 32 | 3.07e-03 | -0.302000 | 1.32e-02 |
| Asparagine N-linked glycosylation | 279 | 4.11e-18 | -0.302000 | 2.16e-16 |
| Defective B4GALT7 causes EDS, progeroid type | 17 | 3.12e-02 | -0.302000 | 9.53e-02 |
| Mitochondrial translation | 94 | 4.30e-07 | -0.302000 | 4.08e-06 |
| Negative regulation of MAPK pathway | 42 | 7.23e-04 | -0.302000 | 3.74e-03 |
| ECM proteoglycans | 61 | 4.77e-05 | -0.301000 | 3.14e-04 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 16 | 3.71e-02 | -0.301000 | 1.07e-01 |
| Nucleotide salvage | 21 | 1.74e-02 | -0.300000 | 5.88e-02 |
| Senescence-Associated Secretory Phenotype (SASP) | 56 | 1.24e-04 | -0.297000 | 7.57e-04 |
| COPI-independent Golgi-to-ER retrograde traffic | 45 | 5.90e-04 | -0.296000 | 3.09e-03 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 35 | 2.47e-03 | -0.296000 | 1.09e-02 |
| FCGR activation | 19 | 2.58e-02 | -0.295000 | 8.10e-02 |
| Generation of second messenger molecules | 21 | 1.96e-02 | -0.294000 | 6.47e-02 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | 17 | 3.59e-02 | -0.294000 | 1.06e-01 |
| Acyl chain remodelling of PC | 17 | 3.65e-02 | 0.293000 | 1.07e-01 |
| Defective B3GAT3 causes JDSSDHD | 17 | 3.66e-02 | -0.293000 | 1.07e-01 |
| Pexophagy | 11 | 9.28e-02 | -0.293000 | 2.09e-01 |
| Unblocking of NMDA receptors, glutamate binding and activation | 17 | 3.67e-02 | -0.293000 | 1.07e-01 |
| UCH proteinases | 85 | 3.13e-06 | -0.293000 | 2.46e-05 |
| APC/C-mediated degradation of cell cycle proteins | 84 | 3.59e-06 | -0.293000 | 2.75e-05 |
| Regulation of mitotic cell cycle | 84 | 3.59e-06 | -0.293000 | 2.75e-05 |
| Late endosomal microautophagy | 32 | 4.20e-03 | -0.292000 | 1.71e-02 |
| ER-Phagosome pathway | 79 | 7.48e-06 | -0.292000 | 5.50e-05 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | 16 | 4.39e-02 | -0.291000 | 1.20e-01 |
| Cleavage of the damaged purine | 15 | 5.32e-02 | -0.288000 | 1.38e-01 |
| Depurination | 15 | 5.32e-02 | -0.288000 | 1.38e-01 |
| Recognition and association of DNA glycosylase with site containing an affected purine | 15 | 5.32e-02 | -0.288000 | 1.38e-01 |
| Cellular response to chemical stress | 183 | 2.08e-11 | -0.287000 | 5.79e-10 |
| Extracellular matrix organization | 250 | 5.80e-15 | -0.287000 | 2.13e-13 |
| RAS processing | 21 | 2.34e-02 | -0.286000 | 7.44e-02 |
| The citric acid (TCA) cycle and respiratory electron transport | 160 | 4.92e-10 | -0.285000 | 1.08e-08 |
| MET activates RAP1 and RAC1 | 11 | 1.02e-01 | 0.285000 | 2.24e-01 |
| Glycosaminoglycan metabolism | 110 | 2.48e-07 | -0.285000 | 2.53e-06 |
| NFE2L2 regulating anti-oxidant/detoxification enzymes | 14 | 6.50e-02 | -0.285000 | 1.59e-01 |
| MAPK6/MAPK4 signaling | 83 | 8.08e-06 | -0.283000 | 5.92e-05 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | 87 | 5.09e-06 | -0.283000 | 3.86e-05 |
| tRNA Aminoacylation | 42 | 1.54e-03 | -0.283000 | 7.22e-03 |
| VLDLR internalisation and degradation | 15 | 5.82e-02 | -0.283000 | 1.47e-01 |
| Translation of Structural Proteins 9694635 | 57 | 2.58e-04 | -0.280000 | 1.47e-03 |
| Regulation of TP53 Expression and Degradation | 36 | 3.68e-03 | -0.280000 | 1.53e-02 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 13 | 8.20e-02 | -0.279000 | 1.90e-01 |
| Hedgehog ‘off’ state | 106 | 7.96e-07 | -0.278000 | 7.15e-06 |
| Non-integrin membrane-ECM interactions | 54 | 4.28e-04 | -0.277000 | 2.30e-03 |
| Synthesis of PIPs at the early endosome membrane | 16 | 5.51e-02 | 0.277000 | 1.41e-01 |
| Metabolism of amino acids and derivatives | 316 | 2.94e-17 | -0.277000 | 1.40e-15 |
| ERKs are inactivated | 13 | 8.41e-02 | -0.277000 | 1.94e-01 |
| DNA Replication Pre-Initiation | 102 | 1.42e-06 | -0.276000 | 1.18e-05 |
| Ras activation upon Ca2+ influx through NMDA receptor | 16 | 5.68e-02 | -0.275000 | 1.44e-01 |
| Cyclin D associated events in G1 | 47 | 1.14e-03 | -0.274000 | 5.57e-03 |
| G1 Phase | 47 | 1.14e-03 | -0.274000 | 5.57e-03 |
| Spry regulation of FGF signaling | 16 | 5.75e-02 | -0.274000 | 1.45e-01 |
| Uptake and actions of bacterial toxins | 25 | 1.77e-02 | -0.274000 | 5.99e-02 |
| Cellular responses to stimuli | 702 | 6.05e-35 | -0.274000 | 4.45e-32 |
| Telomere Extension By Telomerase | 21 | 3.03e-02 | -0.273000 | 9.30e-02 |
| Translesion Synthesis by POLH | 18 | 4.53e-02 | -0.273000 | 1.22e-01 |
| Platelet Adhesion to exposed collagen | 11 | 1.18e-01 | -0.272000 | 2.48e-01 |
| Gap junction trafficking | 32 | 7.77e-03 | -0.272000 | 2.95e-02 |
| Mitotic G1 phase and G1/S transition | 143 | 2.05e-08 | -0.272000 | 2.69e-07 |
| Polo-like kinase mediated events | 14 | 7.83e-02 | -0.272000 | 1.83e-01 |
| IRAK2 mediated activation of TAK1 complex | 10 | 1.37e-01 | -0.272000 | 2.78e-01 |
| Diseases associated with N-glycosylation of proteins | 20 | 3.54e-02 | -0.272000 | 1.05e-01 |
| Selective autophagy | 72 | 6.81e-05 | -0.272000 | 4.41e-04 |
| Transport of bile salts and organic acids, metal ions and amine compounds | 46 | 1.44e-03 | -0.272000 | 6.87e-03 |
| Formation of paraxial mesoderm | 63 | 1.98e-04 | -0.271000 | 1.15e-03 |
| Late SARS-CoV-2 Infection Events | 66 | 1.44e-04 | -0.271000 | 8.77e-04 |
| AKT phosphorylates targets in the nucleus | 10 | 1.39e-01 | -0.270000 | 2.80e-01 |
| Signaling by CSF3 (G-CSF) | 29 | 1.18e-02 | -0.270000 | 4.25e-02 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 14 | 8.05e-02 | -0.270000 | 1.87e-01 |
| Establishment of Sister Chromatid Cohesion | 11 | 1.22e-01 | 0.270000 | 2.52e-01 |
| rRNA modification in the nucleus and cytosol | 59 | 3.57e-04 | -0.269000 | 1.94e-03 |
| Cellular responses to stress | 693 | 4.77e-33 | -0.268000 | 2.34e-30 |
| cGMP effects | 13 | 9.54e-02 | 0.267000 | 2.14e-01 |
| DCC mediated attractive signaling | 13 | 9.58e-02 | 0.267000 | 2.14e-01 |
| Peroxisomal lipid metabolism | 26 | 1.88e-02 | 0.266000 | 6.26e-02 |
| Signalling to RAS | 20 | 4.05e-02 | -0.265000 | 1.15e-01 |
| Interleukin-1 family signaling | 137 | 1.00e-07 | -0.264000 | 1.15e-06 |
| Processing of Intronless Pre-mRNAs | 20 | 4.14e-02 | 0.263000 | 1.17e-01 |
| Signaling by Insulin receptor | 65 | 2.56e-04 | -0.262000 | 1.46e-03 |
| Signaling by the B Cell Receptor (BCR) | 109 | 2.28e-06 | -0.262000 | 1.81e-05 |
| Formation of the beta-catenin:TCF transactivating complex | 36 | 6.58e-03 | -0.262000 | 2.55e-02 |
| Interleukin-15 signaling | 14 | 9.00e-02 | -0.262000 | 2.05e-01 |
| Regulation of TP53 Degradation | 35 | 7.40e-03 | -0.262000 | 2.82e-02 |
| Alpha-protein kinase 1 signaling pathway | 11 | 1.33e-01 | -0.261000 | 2.73e-01 |
| MECP2 regulates neuronal receptors and channels | 15 | 7.98e-02 | -0.261000 | 1.86e-01 |
| Elevation of cytosolic Ca2+ levels | 13 | 1.03e-01 | -0.261000 | 2.27e-01 |
| Peptide ligand-binding receptors | 81 | 5.18e-05 | -0.260000 | 3.40e-04 |
| Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 10 | 1.55e-01 | 0.260000 | 3.05e-01 |
| Regulation of IFNA/IFNB signaling | 12 | 1.20e-01 | -0.260000 | 2.49e-01 |
| Gap junction trafficking and regulation | 34 | 9.12e-03 | -0.258000 | 3.40e-02 |
| G1/S Transition | 125 | 8.21e-07 | -0.255000 | 7.32e-06 |
| Initiation of Nuclear Envelope (NE) Reformation | 19 | 5.40e-02 | -0.255000 | 1.39e-01 |
| Metabolism of carbohydrates | 256 | 2.17e-12 | -0.255000 | 6.50e-11 |
| Nucleotide-like (purinergic) receptors | 15 | 8.76e-02 | 0.255000 | 2.00e-01 |
| NOTCH4 Intracellular Domain Regulates Transcription | 19 | 5.52e-02 | 0.254000 | 1.41e-01 |
| CASP8 activity is inhibited | 10 | 1.66e-01 | -0.253000 | 3.17e-01 |
| Dimerization of procaspase-8 | 10 | 1.66e-01 | -0.253000 | 3.17e-01 |
| Regulation by c-FLIP | 10 | 1.66e-01 | -0.253000 | 3.17e-01 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 12 | 1.29e-01 | 0.253000 | 2.64e-01 |
| GABA synthesis, release, reuptake and degradation | 13 | 1.15e-01 | -0.253000 | 2.43e-01 |
| WNT5A-dependent internalization of FZD4 | 14 | 1.02e-01 | -0.252000 | 2.26e-01 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 42 | 4.73e-03 | -0.252000 | 1.89e-02 |
| HIV Transcription Elongation | 42 | 4.73e-03 | -0.252000 | 1.89e-02 |
| Tat-mediated elongation of the HIV-1 transcript | 42 | 4.73e-03 | -0.252000 | 1.89e-02 |
| NPAS4 regulates expression of target genes | 18 | 6.55e-02 | -0.251000 | 1.59e-01 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 19 | 5.96e-02 | -0.250000 | 1.48e-01 |
| Interleukin-35 Signalling | 10 | 1.72e-01 | -0.250000 | 3.25e-01 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 34 | 1.18e-02 | -0.250000 | 4.25e-02 |
| Degradation of the extracellular matrix | 110 | 7.28e-06 | -0.248000 | 5.38e-05 |
| FRS-mediated FGFR3 signaling | 14 | 1.10e-01 | -0.247000 | 2.37e-01 |
| Signaling by Interleukins | 388 | 9.99e-17 | -0.246000 | 4.46e-15 |
| Carboxyterminal post-translational modifications of tubulin | 30 | 1.97e-02 | -0.246000 | 6.50e-02 |
| PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 14 | 1.12e-01 | 0.246000 | 2.38e-01 |
| p75NTR recruits signalling complexes | 13 | 1.27e-01 | -0.244000 | 2.62e-01 |
| Peptide hormone metabolism | 51 | 2.57e-03 | -0.244000 | 1.12e-02 |
| Cytochrome c-mediated apoptotic response | 13 | 1.28e-01 | 0.244000 | 2.63e-01 |
| Surfactant metabolism | 19 | 6.69e-02 | 0.243000 | 1.62e-01 |
| Signaling by NOTCH4 | 81 | 1.60e-04 | -0.243000 | 9.61e-04 |
| Interleukin-12 family signaling | 47 | 4.12e-03 | -0.242000 | 1.69e-02 |
| Glucose metabolism | 82 | 1.55e-04 | -0.242000 | 9.32e-04 |
| Chaperonin-mediated protein folding | 77 | 2.48e-04 | -0.242000 | 1.43e-03 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 14 | 1.18e-01 | -0.241000 | 2.48e-01 |
| Defective EXT2 causes exostoses 2 | 14 | 1.18e-01 | -0.241000 | 2.48e-01 |
| Mismatch Repair | 14 | 1.18e-01 | -0.241000 | 2.48e-01 |
| Purine catabolism | 13 | 1.32e-01 | -0.241000 | 2.71e-01 |
| Base-Excision Repair, AP Site Formation | 22 | 5.07e-02 | -0.241000 | 1.34e-01 |
| Fc epsilon receptor (FCERI) signaling | 131 | 2.04e-06 | -0.240000 | 1.64e-05 |
| Formation of RNA Pol II elongation complex | 56 | 1.92e-03 | -0.240000 | 8.85e-03 |
| RNA Polymerase II Transcription Elongation | 56 | 1.92e-03 | -0.240000 | 8.85e-03 |
| Transcriptional regulation by RUNX1 | 164 | 1.41e-07 | -0.238000 | 1.56e-06 |
| Metalloprotease DUBs | 19 | 7.20e-02 | -0.238000 | 1.73e-01 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 23 | 4.81e-02 | -0.238000 | 1.29e-01 |
| Metabolism of nucleotides | 82 | 1.97e-04 | -0.238000 | 1.15e-03 |
| Nitric oxide stimulates guanylate cyclase | 16 | 1.00e-01 | 0.237000 | 2.22e-01 |
| Classical antibody-mediated complement activation | 13 | 1.40e-01 | -0.237000 | 2.81e-01 |
| Molecules associated with elastic fibres | 33 | 1.91e-02 | -0.236000 | 6.35e-02 |
| Receptor Mediated Mitophagy | 11 | 1.77e-01 | -0.235000 | 3.30e-01 |
| Role of phospholipids in phagocytosis | 30 | 2.59e-02 | -0.235000 | 8.11e-02 |
| Platelet sensitization by LDL | 17 | 9.39e-02 | -0.235000 | 2.11e-01 |
| CLEC7A (Dectin-1) induces NFAT activation | 11 | 1.78e-01 | -0.234000 | 3.31e-01 |
| Platelet calcium homeostasis | 22 | 5.78e-02 | -0.234000 | 1.46e-01 |
| Signaling by FGFR2 in disease | 34 | 1.84e-02 | -0.234000 | 6.19e-02 |
| ABC-family proteins mediated transport | 92 | 1.14e-04 | -0.233000 | 7.04e-04 |
| Amino acids regulate mTORC1 | 50 | 4.42e-03 | -0.233000 | 1.79e-02 |
| Signaling by Hedgehog | 140 | 2.10e-06 | -0.232000 | 1.68e-05 |
| Detoxification of Reactive Oxygen Species | 33 | 2.10e-02 | -0.232000 | 6.77e-02 |
| Signaling by FGFR4 in disease | 10 | 2.04e-01 | 0.232000 | 3.65e-01 |
| Formation of the Early Elongation Complex | 33 | 2.12e-02 | -0.232000 | 6.80e-02 |
| Formation of the HIV-1 Early Elongation Complex | 33 | 2.12e-02 | -0.232000 | 6.80e-02 |
| Synthesis of DNA | 116 | 1.64e-05 | -0.232000 | 1.14e-04 |
| Uptake and function of anthrax toxins | 11 | 1.84e-01 | -0.231000 | 3.38e-01 |
| DNA Replication | 127 | 6.80e-06 | -0.231000 | 5.08e-05 |
| SHC-mediated cascade:FGFR1 | 13 | 1.49e-01 | -0.231000 | 2.96e-01 |
| MET activates PTK2 signaling | 30 | 2.96e-02 | -0.230000 | 9.11e-02 |
| RORA activates gene expression | 18 | 9.23e-02 | 0.229000 | 2.09e-01 |
| Gastrulation | 86 | 2.44e-04 | -0.229000 | 1.41e-03 |
| FRS-mediated FGFR2 signaling | 16 | 1.14e-01 | -0.228000 | 2.42e-01 |
| Cell surface interactions at the vascular wall | 111 | 3.32e-05 | -0.228000 | 2.24e-04 |
| Synthesis of PIPs at the Golgi membrane | 15 | 1.27e-01 | 0.228000 | 2.62e-01 |
| Antigen processing-Cross presentation | 92 | 1.64e-04 | -0.227000 | 9.79e-04 |
| Cholesterol biosynthesis | 26 | 4.47e-02 | -0.227000 | 1.22e-01 |
| Regulation of TP53 Activity through Acetylation | 29 | 3.41e-02 | -0.227000 | 1.02e-01 |
| PI-3K cascade:FGFR3 | 12 | 1.73e-01 | -0.227000 | 3.26e-01 |
| Association of TriC/CCT with target proteins during biosynthesis | 35 | 2.01e-02 | -0.227000 | 6.56e-02 |
| PIWI-interacting RNA (piRNA) biogenesis | 22 | 6.52e-02 | -0.227000 | 1.59e-01 |
| G2/M Checkpoints | 124 | 1.30e-05 | -0.227000 | 9.27e-05 |
| Attachment and Entry 9694614 | 16 | 1.17e-01 | -0.227000 | 2.46e-01 |
| TAK1-dependent IKK and NF-kappa-B activation | 43 | 1.02e-02 | -0.226000 | 3.73e-02 |
| Pyruvate metabolism | 27 | 4.26e-02 | -0.226000 | 1.18e-01 |
| Nucleotide biosynthesis | 12 | 1.76e-01 | -0.225000 | 3.30e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE | 27 | 4.26e-02 | -0.225000 | 1.18e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 27 | 4.26e-02 | -0.225000 | 1.18e-01 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 42 | 1.16e-02 | -0.225000 | 4.20e-02 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | 16 | 1.20e-01 | 0.225000 | 2.49e-01 |
| Incretin synthesis, secretion, and inactivation | 12 | 1.78e-01 | -0.225000 | 3.31e-01 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 12 | 1.78e-01 | -0.225000 | 3.31e-01 |
| Signaling by FGFR3 | 34 | 2.34e-02 | -0.225000 | 7.44e-02 |
| TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling | 13 | 1.61e-01 | -0.225000 | 3.11e-01 |
| DNA Double Strand Break Response | 43 | 1.09e-02 | -0.224000 | 3.97e-02 |
| Regulation of CDH11 gene transcription | 10 | 2.20e-01 | -0.224000 | 3.83e-01 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 17 | 1.10e-01 | -0.224000 | 2.37e-01 |
| Leading Strand Synthesis | 14 | 1.47e-01 | 0.224000 | 2.92e-01 |
| Polymerase switching | 14 | 1.47e-01 | 0.224000 | 2.92e-01 |
| Expression and translocation of olfactory receptors | 21 | 7.57e-02 | 0.224000 | 1.79e-01 |
| PTEN Regulation | 137 | 6.38e-06 | -0.224000 | 4.78e-05 |
| Protein folding | 83 | 4.37e-04 | -0.223000 | 2.34e-03 |
| VEGFR2 mediated cell proliferation | 19 | 9.36e-02 | -0.222000 | 2.11e-01 |
| Nuclear Events (kinase and transcription factor activation) | 57 | 3.80e-03 | -0.222000 | 1.57e-02 |
| RIP-mediated NFkB activation via ZBP1 | 17 | 1.14e-01 | -0.221000 | 2.42e-01 |
| Constitutive Signaling by AKT1 E17K in Cancer | 26 | 5.11e-02 | -0.221000 | 1.35e-01 |
| Kinesins | 47 | 9.04e-03 | -0.220000 | 3.38e-02 |
| Platelet degranulation | 110 | 6.96e-05 | -0.220000 | 4.45e-04 |
| FGFR2 alternative splicing | 24 | 6.28e-02 | -0.219000 | 1.55e-01 |
| Axon guidance | 487 | 1.38e-16 | -0.219000 | 5.96e-15 |
| Nervous system development | 507 | 3.46e-17 | -0.219000 | 1.59e-15 |
| Downregulation of TGF-beta receptor signaling | 26 | 5.37e-02 | -0.219000 | 1.39e-01 |
| Formation of HIV elongation complex in the absence of HIV Tat | 44 | 1.22e-02 | -0.219000 | 4.36e-02 |
| Cleavage of the damaged pyrimidine | 20 | 9.09e-02 | -0.218000 | 2.06e-01 |
| Depyrimidination | 20 | 9.09e-02 | -0.218000 | 2.06e-01 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 20 | 9.09e-02 | -0.218000 | 2.06e-01 |
| RNA Polymerase III Chain Elongation | 18 | 1.10e-01 | -0.218000 | 2.37e-01 |
| Formation of the cornified envelope | 23 | 7.07e-02 | -0.218000 | 1.70e-01 |
| Keratinization | 23 | 7.07e-02 | -0.218000 | 1.70e-01 |
| Signaling by PDGFRA extracellular domain mutants | 12 | 1.92e-01 | -0.218000 | 3.49e-01 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 12 | 1.92e-01 | -0.218000 | 3.49e-01 |
| Regulation of gene expression by Hypoxia-inducible Factor | 10 | 2.34e-01 | -0.217000 | 4.02e-01 |
| Nuclear Envelope (NE) Reassembly | 68 | 1.96e-03 | -0.217000 | 8.96e-03 |
| Glycogen metabolism | 23 | 7.35e-02 | -0.216000 | 1.75e-01 |
| Translesion synthesis by REV1 | 16 | 1.36e-01 | -0.215000 | 2.78e-01 |
| RA biosynthesis pathway | 16 | 1.37e-01 | 0.215000 | 2.78e-01 |
| Nuclear events stimulated by ALK signaling in cancer | 19 | 1.05e-01 | -0.215000 | 2.30e-01 |
| Activation of BAD and translocation to mitochondria | 15 | 1.50e-01 | -0.215000 | 2.97e-01 |
| SARS-CoV-1-host interactions | 94 | 3.28e-04 | -0.214000 | 1.82e-03 |
| Viral Infection Pathways | 662 | 1.14e-20 | -0.213000 | 1.12e-18 |
| Bacterial Infection Pathways | 65 | 3.00e-03 | -0.213000 | 1.30e-02 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 33 | 3.47e-02 | 0.212000 | 1.03e-01 |
| TRP channels | 20 | 1.00e-01 | 0.212000 | 2.22e-01 |
| Signaling by FGFR2 | 61 | 4.18e-03 | -0.212000 | 1.71e-02 |
| Response to elevated platelet cytosolic Ca2+ | 114 | 9.32e-05 | -0.212000 | 5.86e-04 |
| RNA Polymerase II Pre-transcription Events | 77 | 1.35e-03 | -0.211000 | 6.49e-03 |
| Mitotic G2-G2/M phases | 187 | 6.56e-07 | -0.211000 | 6.10e-06 |
| C-type lectin receptors (CLRs) | 122 | 5.76e-05 | -0.211000 | 3.77e-04 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 11 | 2.26e-01 | -0.211000 | 3.92e-01 |
| G-protein beta:gamma signalling | 27 | 5.87e-02 | 0.210000 | 1.47e-01 |
| MHC class II antigen presentation | 97 | 3.53e-04 | -0.210000 | 1.94e-03 |
| G2/M Transition | 185 | 9.19e-07 | -0.209000 | 7.95e-06 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 13 | 1.91e-01 | -0.209000 | 3.49e-01 |
| PI-3K cascade:FGFR2 | 14 | 1.76e-01 | -0.209000 | 3.29e-01 |
| HIV Infection | 223 | 8.01e-08 | -0.209000 | 9.43e-07 |
| TGF-beta receptor signaling activates SMADs | 45 | 1.58e-02 | -0.208000 | 5.43e-02 |
| activated TAK1 mediates p38 MAPK activation | 23 | 8.44e-02 | -0.208000 | 1.94e-01 |
| Separation of Sister Chromatids | 175 | 2.24e-06 | -0.208000 | 1.78e-05 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 13 | 1.96e-01 | -0.207000 | 3.53e-01 |
| Regulation of TNFR1 signaling | 48 | 1.32e-02 | -0.207000 | 4.70e-02 |
| Metabolism of proteins | 1630 | 3.72e-43 | -0.207000 | 5.48e-40 |
| PERK regulates gene expression | 32 | 4.36e-02 | -0.206000 | 1.20e-01 |
| Signaling by FGFR4 | 32 | 4.36e-02 | -0.206000 | 1.20e-01 |
| Acyl chain remodelling of PE | 17 | 1.42e-01 | 0.206000 | 2.85e-01 |
| Metabolism of fat-soluble vitamins | 32 | 4.43e-02 | -0.205000 | 1.21e-01 |
| TICAM1,TRAF6-dependent induction of TAK1 complex | 11 | 2.39e-01 | -0.205000 | 4.08e-01 |
| NRIF signals cell death from the nucleus | 16 | 1.57e-01 | -0.205000 | 3.07e-01 |
| Neutrophil degranulation | 423 | 6.57e-13 | -0.204000 | 2.10e-11 |
| Glycolysis | 65 | 4.46e-03 | -0.204000 | 1.80e-02 |
| Negative regulation of FGFR1 signaling | 25 | 7.79e-02 | -0.204000 | 1.83e-01 |
| RAF-independent MAPK1/3 activation | 22 | 9.82e-02 | -0.204000 | 2.18e-01 |
| Processive synthesis on the C-strand of the telomere | 19 | 1.24e-01 | -0.204000 | 2.57e-01 |
| TNFR1-induced NF-kappa-B signaling pathway | 33 | 4.40e-02 | -0.203000 | 1.20e-01 |
| Host Interactions of HIV factors | 127 | 8.21e-05 | -0.202000 | 5.23e-04 |
| TRAF3-dependent IRF activation pathway | 13 | 2.07e-01 | 0.202000 | 3.67e-01 |
| Activation of BH3-only proteins | 28 | 6.45e-02 | -0.202000 | 1.58e-01 |
| Synthesis of PIPs at the late endosome membrane | 11 | 2.46e-01 | 0.202000 | 4.20e-01 |
| TNFR1-induced proapoptotic signaling | 25 | 8.09e-02 | -0.202000 | 1.88e-01 |
| Regulation of Complement cascade | 37 | 3.38e-02 | -0.202000 | 1.01e-01 |
| Protein localization | 155 | 1.51e-05 | -0.202000 | 1.07e-04 |
| Recycling pathway of L1 | 41 | 2.57e-02 | -0.201000 | 8.08e-02 |
| Creation of C4 and C2 activators | 16 | 1.64e-01 | -0.201000 | 3.15e-01 |
| FRS-mediated FGFR4 signaling | 13 | 2.09e-01 | -0.201000 | 3.70e-01 |
| DNA Damage Recognition in GG-NER | 38 | 3.20e-02 | -0.201000 | 9.68e-02 |
| Purine salvage | 12 | 2.28e-01 | -0.201000 | 3.93e-01 |
| ER Quality Control Compartment (ERQC) | 21 | 1.11e-01 | -0.201000 | 2.38e-01 |
| Regulation of CDH11 function | 10 | 2.71e-01 | -0.201000 | 4.52e-01 |
| mRNA decay by 5’ to 3’ exoribonuclease | 15 | 1.78e-01 | -0.201000 | 3.31e-01 |
| Signaling by FGFR | 70 | 3.72e-03 | -0.201000 | 1.54e-02 |
| Synthesis of substrates in N-glycan biosythesis | 58 | 8.30e-03 | -0.200000 | 3.12e-02 |
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 16 | 1.68e-01 | 0.199000 | 3.20e-01 |
| Plasma lipoprotein assembly | 11 | 2.52e-01 | 0.199000 | 4.28e-01 |
| Citric acid cycle (TCA cycle) | 22 | 1.08e-01 | -0.198000 | 2.33e-01 |
| Diseases of glycosylation | 127 | 1.16e-04 | -0.198000 | 7.17e-04 |
| Metabolic disorders of biological oxidation enzymes | 23 | 1.01e-01 | -0.198000 | 2.23e-01 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 73 | 3.58e-03 | -0.197000 | 1.49e-02 |
| TNFs bind their physiological receptors | 19 | 1.37e-01 | -0.197000 | 2.79e-01 |
| mRNA Splicing - Minor Pathway | 50 | 1.64e-02 | -0.196000 | 5.63e-02 |
| Mitotic Anaphase | 218 | 6.60e-07 | -0.196000 | 6.10e-06 |
| Oxidative Stress Induced Senescence | 69 | 4.96e-03 | -0.196000 | 1.97e-02 |
| Autophagy | 139 | 6.95e-05 | -0.196000 | 4.45e-04 |
| Transcription of the HIV genome | 67 | 5.69e-03 | -0.195000 | 2.23e-02 |
| SARS-CoV-1 Infection | 136 | 8.59e-05 | -0.195000 | 5.44e-04 |
| RHOBTB1 GTPase cycle | 23 | 1.06e-01 | 0.195000 | 2.30e-01 |
| RMTs methylate histone arginines | 33 | 5.26e-02 | -0.195000 | 1.38e-01 |
| RAF/MAP kinase cascade | 234 | 3.07e-07 | -0.195000 | 3.05e-06 |
| TP53 Regulates Transcription of DNA Repair Genes | 61 | 8.65e-03 | -0.194000 | 3.24e-02 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 29 | 7.08e-02 | -0.194000 | 1.70e-01 |
| Activation of IRF3, IRF7 mediated by TBK1, IKBKE | 17 | 1.67e-01 | -0.194000 | 3.19e-01 |
| MET receptor recycling | 10 | 2.89e-01 | 0.194000 | 4.71e-01 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | 186 | 5.60e-06 | -0.193000 | 4.22e-05 |
| Diseases of carbohydrate metabolism | 28 | 7.69e-02 | -0.193000 | 1.81e-01 |
| Receptor-type tyrosine-protein phosphatases | 12 | 2.48e-01 | -0.193000 | 4.22e-01 |
| Mitotic Metaphase and Anaphase | 219 | 9.14e-07 | -0.193000 | 7.95e-06 |
| Pre-NOTCH Processing in Golgi | 18 | 1.57e-01 | -0.192000 | 3.08e-01 |
| Toll Like Receptor 3 (TLR3) Cascade | 103 | 7.54e-04 | -0.192000 | 3.87e-03 |
| mRNA Capping | 29 | 7.37e-02 | -0.192000 | 1.75e-01 |
| Adenylate cyclase activating pathway | 10 | 2.94e-01 | 0.192000 | 4.76e-01 |
| Interleukin-12 signaling | 41 | 3.38e-02 | -0.192000 | 1.01e-01 |
| Gastrin-CREB signalling pathway via PKC and MAPK | 16 | 1.85e-01 | 0.192000 | 3.38e-01 |
| NS1 Mediated Effects on Host Pathways | 40 | 3.69e-02 | 0.191000 | 1.07e-01 |
| MAPK1/MAPK3 signaling | 240 | 3.97e-07 | -0.190000 | 3.79e-06 |
| Regulation of IFNG signaling | 13 | 2.36e-01 | -0.190000 | 4.06e-01 |
| Regulation of PTEN mRNA translation | 11 | 2.76e-01 | 0.190000 | 4.57e-01 |
| Formation of WDR5-containing histone-modifying complexes | 42 | 3.34e-02 | 0.190000 | 1.01e-01 |
| Infectious disease | 836 | 1.88e-20 | -0.190000 | 1.63e-18 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 95 | 1.42e-03 | -0.189000 | 6.81e-03 |
| O-linked glycosylation of mucins | 42 | 3.37e-02 | -0.189000 | 1.01e-01 |
| Transcriptional regulation of granulopoiesis | 33 | 6.00e-02 | -0.189000 | 1.49e-01 |
| Beta-catenin independent WNT signaling | 133 | 1.86e-04 | -0.188000 | 1.10e-03 |
| Chaperone Mediated Autophagy | 20 | 1.47e-01 | -0.188000 | 2.92e-01 |
| Retrograde neurotrophin signalling | 14 | 2.27e-01 | -0.187000 | 3.93e-01 |
| Amyloid fiber formation | 41 | 3.90e-02 | -0.186000 | 1.11e-01 |
| Amino acid transport across the plasma membrane | 20 | 1.50e-01 | -0.186000 | 2.97e-01 |
| PIP3 activates AKT signaling | 242 | 6.70e-07 | -0.186000 | 6.12e-06 |
| Ion homeostasis | 43 | 3.52e-02 | -0.186000 | 1.04e-01 |
| Glycosphingolipid metabolism | 36 | 5.50e-02 | -0.185000 | 1.41e-01 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 11 | 2.90e-01 | -0.184000 | 4.72e-01 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 40 | 4.41e-02 | -0.184000 | 1.21e-01 |
| Apoptotic cleavage of cellular proteins | 34 | 6.35e-02 | 0.184000 | 1.56e-01 |
| Signaling by WNT | 242 | 9.14e-07 | -0.183000 | 7.95e-06 |
| DNA methylation | 10 | 3.19e-01 | -0.182000 | 5.04e-01 |
| Metabolism of cofactors | 18 | 1.82e-01 | -0.182000 | 3.37e-01 |
| Signaling by PDGF | 53 | 2.22e-02 | -0.182000 | 7.10e-02 |
| Azathioprine ADME | 18 | 1.83e-01 | -0.181000 | 3.37e-01 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 22 | 1.41e-01 | -0.181000 | 2.83e-01 |
| Signaling by NTRK1 (TRKA) | 108 | 1.19e-03 | -0.181000 | 5.80e-03 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 15 | 2.27e-01 | 0.180000 | 3.93e-01 |
| Pregnenolone biosynthesis | 10 | 3.25e-01 | -0.180000 | 5.09e-01 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 23 | 1.38e-01 | -0.179000 | 2.80e-01 |
| Binding and Uptake of Ligands by Scavenger Receptors | 38 | 5.75e-02 | -0.178000 | 1.45e-01 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | 11 | 3.07e-01 | -0.178000 | 4.91e-01 |
| DNA Damage/Telomere Stress Induced Senescence | 33 | 7.76e-02 | -0.178000 | 1.82e-01 |
| Mitotic Telophase/Cytokinesis | 13 | 2.71e-01 | 0.176000 | 4.52e-01 |
| Post-translational modification: synthesis of GPI-anchored proteins | 62 | 1.65e-02 | -0.176000 | 5.63e-02 |
| NR1H2 and NR1H3-mediated signaling | 40 | 5.48e-02 | 0.176000 | 1.41e-01 |
| Regulation of RUNX1 Expression and Activity | 18 | 1.98e-01 | -0.175000 | 3.55e-01 |
| Cyclin A/B1/B2 associated events during G2/M transition | 22 | 1.55e-01 | -0.175000 | 3.05e-01 |
| HIV Transcription Initiation | 45 | 4.21e-02 | -0.175000 | 1.17e-01 |
| RNA Polymerase II HIV Promoter Escape | 45 | 4.21e-02 | -0.175000 | 1.17e-01 |
| RNA Polymerase II Promoter Escape | 45 | 4.21e-02 | -0.175000 | 1.17e-01 |
| RNA Polymerase II Transcription Initiation | 45 | 4.21e-02 | -0.175000 | 1.17e-01 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 45 | 4.21e-02 | -0.175000 | 1.17e-01 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 45 | 4.21e-02 | -0.175000 | 1.17e-01 |
| Metabolism of folate and pterines | 16 | 2.25e-01 | -0.175000 | 3.92e-01 |
| Macroautophagy | 125 | 7.32e-04 | -0.175000 | 3.78e-03 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 22 | 1.56e-01 | -0.175000 | 3.06e-01 |
| Deactivation of the beta-catenin transactivating complex | 39 | 5.88e-02 | -0.175000 | 1.47e-01 |
| Regulation of FZD by ubiquitination | 16 | 2.26e-01 | -0.175000 | 3.92e-01 |
| RUNX2 regulates osteoblast differentiation | 22 | 1.56e-01 | -0.175000 | 3.06e-01 |
| Repression of WNT target genes | 14 | 2.58e-01 | -0.175000 | 4.35e-01 |
| Costimulation by the CD28 family | 53 | 2.81e-02 | -0.174000 | 8.75e-02 |
| S Phase | 157 | 1.66e-04 | -0.174000 | 9.89e-04 |
| Cytokine Signaling in Immune system | 593 | 5.64e-13 | -0.174000 | 1.85e-11 |
| PI Metabolism | 78 | 8.00e-03 | 0.174000 | 3.02e-02 |
| Oncogene Induced Senescence | 33 | 8.44e-02 | -0.174000 | 1.94e-01 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 32 | 8.96e-02 | -0.173000 | 2.04e-01 |
| Neddylation | 223 | 8.36e-06 | -0.173000 | 6.09e-05 |
| Glutamate Neurotransmitter Release Cycle | 22 | 1.61e-01 | -0.173000 | 3.11e-01 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 36 | 7.33e-02 | -0.173000 | 1.75e-01 |
| Paracetamol ADME | 19 | 1.93e-01 | 0.172000 | 3.50e-01 |
| RUNX3 regulates NOTCH signaling | 14 | 2.64e-01 | 0.172000 | 4.44e-01 |
| Transcription of E2F targets under negative control by DREAM complex | 18 | 2.06e-01 | -0.172000 | 3.65e-01 |
| Translesion synthesis by POLK | 17 | 2.19e-01 | -0.172000 | 3.82e-01 |
| Inflammasomes | 21 | 1.72e-01 | -0.172000 | 3.25e-01 |
| PI-3K cascade:FGFR4 | 11 | 3.24e-01 | -0.172000 | 5.09e-01 |
| TRAF6 mediated IRF7 activation | 15 | 2.51e-01 | 0.171000 | 4.26e-01 |
| Telomere Maintenance | 69 | 1.40e-02 | -0.171000 | 4.94e-02 |
| Muscle contraction | 154 | 2.54e-04 | -0.171000 | 1.45e-03 |
| MyD88-independent TLR4 cascade | 107 | 2.31e-03 | -0.171000 | 1.03e-02 |
| TRIF(TICAM1)-mediated TLR4 signaling | 107 | 2.31e-03 | -0.171000 | 1.03e-02 |
| Retinoid metabolism and transport | 29 | 1.12e-01 | -0.171000 | 2.39e-01 |
| Removal of the Flap Intermediate from the C-strand | 17 | 2.24e-01 | -0.170000 | 3.90e-01 |
| The NLRP3 inflammasome | 16 | 2.38e-01 | -0.170000 | 4.08e-01 |
| Diseases of metabolism | 206 | 2.99e-05 | -0.169000 | 2.04e-04 |
| Blood group systems biosynthesis | 13 | 2.92e-01 | -0.169000 | 4.75e-01 |
| TICAM1, RIP1-mediated IKK complex recruitment | 19 | 2.03e-01 | -0.169000 | 3.64e-01 |
| Cellular Senescence | 132 | 8.43e-04 | -0.168000 | 4.25e-03 |
| MAPK family signaling cascades | 275 | 1.61e-06 | -0.168000 | 1.31e-05 |
| Defects in cobalamin (B12) metabolism | 12 | 3.13e-01 | 0.168000 | 4.96e-01 |
| RAB geranylgeranylation | 56 | 2.96e-02 | -0.168000 | 9.11e-02 |
| Formation of Fibrin Clot (Clotting Cascade) | 20 | 1.93e-01 | -0.168000 | 3.50e-01 |
| Disorders of Developmental Biology | 11 | 3.35e-01 | -0.168000 | 5.18e-01 |
| Disorders of Nervous System Development | 11 | 3.35e-01 | -0.168000 | 5.18e-01 |
| Loss of function of MECP2 in Rett syndrome | 11 | 3.35e-01 | -0.168000 | 5.18e-01 |
| Pervasive developmental disorders | 11 | 3.35e-01 | -0.168000 | 5.18e-01 |
| Apoptosis | 161 | 2.39e-04 | -0.168000 | 1.38e-03 |
| ZBP1(DAI) mediated induction of type I IFNs | 20 | 1.94e-01 | -0.168000 | 3.50e-01 |
| Meiotic recombination | 26 | 1.39e-01 | -0.168000 | 2.80e-01 |
| G alpha (i) signalling events | 181 | 1.04e-04 | -0.167000 | 6.53e-04 |
| Intracellular signaling by second messengers | 279 | 1.58e-06 | -0.167000 | 1.30e-05 |
| Complement cascade | 41 | 6.39e-02 | -0.167000 | 1.57e-01 |
| Downstream signaling of activated FGFR3 | 19 | 2.08e-01 | -0.167000 | 3.67e-01 |
| Transport of the SLBP independent Mature mRNA | 35 | 8.74e-02 | 0.167000 | 2.00e-01 |
| Developmental Biology | 780 | 3.08e-15 | -0.167000 | 1.16e-13 |
| Factors involved in megakaryocyte development and platelet production | 120 | 1.62e-03 | -0.167000 | 7.57e-03 |
| RAF activation | 34 | 9.26e-02 | -0.167000 | 2.09e-01 |
| Integration of energy metabolism | 87 | 7.29e-03 | -0.167000 | 2.79e-02 |
| Apoptotic execution phase | 42 | 6.24e-02 | 0.166000 | 1.54e-01 |
| G beta:gamma signalling through PLC beta | 15 | 2.66e-01 | 0.166000 | 4.46e-01 |
| Fatty acyl-CoA biosynthesis | 30 | 1.16e-01 | -0.166000 | 2.44e-01 |
| Potential therapeutics for SARS | 96 | 4.98e-03 | -0.166000 | 1.97e-02 |
| IGF1R signaling cascade | 39 | 7.42e-02 | -0.165000 | 1.76e-01 |
| Disorders of transmembrane transporters | 139 | 7.82e-04 | -0.165000 | 3.99e-03 |
| Innate Immune System | 870 | 3.20e-16 | -0.164000 | 1.34e-14 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 36 | 8.93e-02 | -0.164000 | 2.04e-01 |
| HCMV Infection | 99 | 4.92e-03 | -0.164000 | 1.96e-02 |
| GPER1 signaling | 38 | 8.17e-02 | -0.163000 | 1.89e-01 |
| Transport of Ribonucleoproteins into the Host Nucleus | 32 | 1.11e-01 | 0.163000 | 2.38e-01 |
| NEP/NS2 Interacts with the Cellular Export Machinery | 32 | 1.11e-01 | 0.163000 | 2.38e-01 |
| RUNX2 regulates bone development | 28 | 1.37e-01 | -0.163000 | 2.78e-01 |
| Hemostasis | 488 | 1.10e-09 | -0.162000 | 2.12e-08 |
| PI3K Cascade | 31 | 1.21e-01 | -0.161000 | 2.52e-01 |
| Downstream signaling of activated FGFR2 | 21 | 2.03e-01 | -0.161000 | 3.63e-01 |
| Other interleukin signaling | 20 | 2.14e-01 | -0.161000 | 3.76e-01 |
| Transport of Mature mRNA Derived from an Intronless Transcript | 42 | 7.26e-02 | 0.160000 | 1.74e-01 |
| Pyruvate metabolism and Citric Acid (TCA) cycle | 51 | 4.82e-02 | -0.160000 | 1.29e-01 |
| Post-translational protein modification | 1192 | 2.93e-20 | -0.160000 | 2.27e-18 |
| L1CAM interactions | 102 | 5.35e-03 | -0.160000 | 2.10e-02 |
| Diseases of programmed cell death | 47 | 5.94e-02 | -0.159000 | 1.48e-01 |
| Signaling by NOTCH | 176 | 2.84e-04 | -0.159000 | 1.60e-03 |
| Signaling by ALK fusions and activated point mutants | 55 | 4.19e-02 | -0.159000 | 1.17e-01 |
| Signaling by ALK in cancer | 55 | 4.19e-02 | -0.159000 | 1.17e-01 |
| GAB1 signalosome | 14 | 3.05e-01 | 0.158000 | 4.88e-01 |
| Ub-specific processing proteases | 156 | 6.51e-04 | -0.158000 | 3.39e-03 |
| PKMTs methylate histone lysines | 42 | 7.62e-02 | 0.158000 | 1.79e-01 |
| Mitochondrial tRNA aminoacylation | 21 | 2.10e-01 | -0.158000 | 3.70e-01 |
| Protein methylation | 15 | 2.90e-01 | -0.158000 | 4.72e-01 |
| RHOV GTPase cycle | 34 | 1.13e-01 | 0.157000 | 2.40e-01 |
| Olfactory Signaling Pathway | 25 | 1.74e-01 | 0.157000 | 3.28e-01 |
| Synaptic adhesion-like molecules | 18 | 2.49e-01 | -0.157000 | 4.23e-01 |
| APC-Cdc20 mediated degradation of Nek2A | 25 | 1.75e-01 | -0.157000 | 3.28e-01 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 24 | 1.85e-01 | -0.156000 | 3.38e-01 |
| Trafficking of AMPA receptors | 24 | 1.85e-01 | -0.156000 | 3.38e-01 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 36 | 1.08e-01 | -0.155000 | 2.33e-01 |
| STING mediated induction of host immune responses | 15 | 3.01e-01 | 0.154000 | 4.84e-01 |
| p38MAPK events | 13 | 3.37e-01 | -0.154000 | 5.19e-01 |
| Base Excision Repair | 50 | 5.99e-02 | -0.154000 | 1.49e-01 |
| Signaling by WNT in cancer | 28 | 1.59e-01 | -0.154000 | 3.09e-01 |
| RIPK1-mediated regulated necrosis | 30 | 1.45e-01 | -0.154000 | 2.91e-01 |
| Regulation of necroptotic cell death | 30 | 1.45e-01 | -0.154000 | 2.91e-01 |
| HS-GAG biosynthesis | 25 | 1.84e-01 | -0.153000 | 3.38e-01 |
| Regulation of pyruvate dehydrogenase (PDH) complex | 15 | 3.04e-01 | -0.153000 | 4.86e-01 |
| Formation of apoptosome | 11 | 3.79e-01 | 0.153000 | 5.71e-01 |
| Regulation of the apoptosome activity | 11 | 3.79e-01 | 0.153000 | 5.71e-01 |
| Trafficking of GluR2-containing AMPA receptors | 14 | 3.22e-01 | -0.153000 | 5.06e-01 |
| Sema4D induced cell migration and growth-cone collapse | 19 | 2.53e-01 | -0.152000 | 4.28e-01 |
| Neurexins and neuroligins | 41 | 9.32e-02 | -0.152000 | 2.10e-01 |
| Signaling by FGFR1 | 40 | 9.75e-02 | -0.151000 | 2.17e-01 |
| Platelet Aggregation (Plug Formation) | 30 | 1.51e-01 | -0.151000 | 2.99e-01 |
| Programmed Cell Death | 188 | 3.54e-04 | -0.151000 | 1.94e-03 |
| Protein-protein interactions at synapses | 63 | 3.86e-02 | -0.151000 | 1.11e-01 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | 25 | 1.92e-01 | -0.151000 | 3.49e-01 |
| Diseases of mitotic cell cycle | 38 | 1.08e-01 | -0.151000 | 2.34e-01 |
| Interleukin-20 family signaling | 14 | 3.30e-01 | -0.151000 | 5.14e-01 |
| Notch-HLH transcription pathway | 28 | 1.68e-01 | 0.150000 | 3.20e-01 |
| Metabolism | 1733 | 8.66e-25 | -0.150000 | 2.55e-22 |
| Signaling by FGFR3 in disease | 16 | 3.00e-01 | -0.150000 | 4.82e-01 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 24 | 2.05e-01 | -0.149000 | 3.65e-01 |
| Immune System | 1632 | 2.65e-23 | -0.149000 | 6.49e-21 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | 11 | 3.91e-01 | 0.149000 | 5.83e-01 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 55 | 5.56e-02 | -0.149000 | 1.42e-01 |
| Initial triggering of complement | 23 | 2.16e-01 | -0.149000 | 3.78e-01 |
| Late Phase of HIV Life Cycle | 132 | 3.16e-03 | -0.149000 | 1.34e-02 |
| Growth hormone receptor signaling | 20 | 2.50e-01 | -0.148000 | 4.25e-01 |
| Transport of the SLBP Dependant Mature mRNA | 36 | 1.27e-01 | 0.147000 | 2.61e-01 |
| MET promotes cell motility | 40 | 1.09e-01 | -0.146000 | 2.36e-01 |
| IRS-related events triggered by IGF1R | 38 | 1.19e-01 | -0.146000 | 2.49e-01 |
| Disease | 1475 | 1.73e-20 | -0.146000 | 1.59e-18 |
| Cell Cycle Checkpoints | 239 | 1.07e-04 | -0.146000 | 6.67e-04 |
| Condensation of Prometaphase Chromosomes | 11 | 4.05e-01 | -0.145000 | 5.97e-01 |
| Translesion synthesis by POLI | 17 | 3.02e-01 | -0.145000 | 4.84e-01 |
| Vpr-mediated nuclear import of PICs | 34 | 1.46e-01 | 0.144000 | 2.91e-01 |
| HIV Life Cycle | 145 | 2.74e-03 | -0.144000 | 1.19e-02 |
| Acyl chain remodelling of PS | 12 | 3.87e-01 | 0.144000 | 5.80e-01 |
| Signaling by FGFR in disease | 53 | 7.01e-02 | -0.144000 | 1.69e-01 |
| Metabolism of RNA | 693 | 1.35e-10 | -0.144000 | 3.42e-09 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | 43 | 1.03e-01 | 0.144000 | 2.27e-01 |
| The phototransduction cascade | 19 | 2.79e-01 | -0.144000 | 4.60e-01 |
| TNF signaling | 57 | 6.10e-02 | -0.143000 | 1.51e-01 |
| MyD88 cascade initiated on plasma membrane | 94 | 1.66e-02 | -0.143000 | 5.65e-02 |
| Toll Like Receptor 10 (TLR10) Cascade | 94 | 1.66e-02 | -0.143000 | 5.65e-02 |
| Toll Like Receptor 5 (TLR5) Cascade | 94 | 1.66e-02 | -0.143000 | 5.65e-02 |
| ATF4 activates genes in response to endoplasmic reticulum stress | 27 | 2.01e-01 | -0.142000 | 3.59e-01 |
| Formation of annular gap junctions | 11 | 4.14e-01 | -0.142000 | 6.06e-01 |
| Cytoprotection by HMOX1 | 58 | 6.20e-02 | -0.142000 | 1.53e-01 |
| Regulation of TP53 Activity through Methylation | 19 | 2.86e-01 | -0.141000 | 4.69e-01 |
| Beta-oxidation of very long chain fatty acids | 10 | 4.40e-01 | 0.141000 | 6.32e-01 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 28 | 1.96e-01 | -0.141000 | 3.53e-01 |
| Signaling by NTRKs | 124 | 6.75e-03 | -0.141000 | 2.61e-02 |
| Dissolution of Fibrin Clot | 10 | 4.40e-01 | -0.141000 | 6.32e-01 |
| Regulation of TP53 Activity | 149 | 3.09e-03 | -0.141000 | 1.32e-02 |
| Cytosolic sensors of pathogen-associated DNA | 63 | 5.41e-02 | -0.140000 | 1.39e-01 |
| Negative regulation of FLT3 | 13 | 3.83e-01 | -0.140000 | 5.75e-01 |
| SLC-mediated transmembrane transport | 152 | 3.04e-03 | -0.139000 | 1.31e-02 |
| GRB2 events in EGFR signaling | 10 | 4.46e-01 | 0.139000 | 6.39e-01 |
| Bile acid and bile salt metabolism | 29 | 1.95e-01 | 0.139000 | 3.52e-01 |
| NCAM1 interactions | 32 | 1.74e-01 | -0.139000 | 3.28e-01 |
| PI3K/AKT Signaling in Cancer | 83 | 2.90e-02 | -0.139000 | 8.97e-02 |
| Signaling by NTRK3 (TRKC) | 17 | 3.23e-01 | -0.139000 | 5.07e-01 |
| Rap1 signalling | 13 | 3.88e-01 | 0.138000 | 5.80e-01 |
| Platelet activation, signaling and aggregation | 222 | 4.03e-04 | -0.138000 | 2.17e-03 |
| Regulation of NF-kappa B signaling | 18 | 3.12e-01 | -0.138000 | 4.96e-01 |
| Signaling by KIT in disease | 20 | 2.89e-01 | -0.137000 | 4.71e-01 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 20 | 2.89e-01 | -0.137000 | 4.71e-01 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 11 | 4.33e-01 | 0.137000 | 6.25e-01 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 108 | 1.44e-02 | -0.136000 | 5.03e-02 |
| Toll Like Receptor 2 (TLR2) Cascade | 108 | 1.44e-02 | -0.136000 | 5.03e-02 |
| Toll Like Receptor TLR1:TLR2 Cascade | 108 | 1.44e-02 | -0.136000 | 5.03e-02 |
| Toll Like Receptor TLR6:TLR2 Cascade | 108 | 1.44e-02 | -0.136000 | 5.03e-02 |
| Sialic acid metabolism | 28 | 2.12e-01 | -0.136000 | 3.74e-01 |
| Nuclear Pore Complex (NPC) Disassembly | 36 | 1.59e-01 | 0.136000 | 3.09e-01 |
| Transcriptional Regulation by TP53 | 340 | 1.78e-05 | -0.136000 | 1.23e-04 |
| Inactivation, recovery and regulation of the phototransduction cascade | 18 | 3.20e-01 | -0.135000 | 5.04e-01 |
| Export of Viral Ribonucleoproteins from Nucleus | 33 | 1.78e-01 | 0.135000 | 3.31e-01 |
| Regulation of actin dynamics for phagocytic cup formation | 67 | 5.57e-02 | -0.135000 | 1.42e-01 |
| Signaling by NODAL | 13 | 4.00e-01 | 0.135000 | 5.93e-01 |
| FOXO-mediated transcription of cell death genes | 15 | 3.67e-01 | -0.135000 | 5.58e-01 |
| Defective pyroptosis | 19 | 3.10e-01 | 0.135000 | 4.94e-01 |
| Basigin interactions | 21 | 2.88e-01 | -0.134000 | 4.71e-01 |
| MAP kinase activation | 63 | 6.76e-02 | -0.133000 | 1.63e-01 |
| Signaling by Receptor Tyrosine Kinases | 469 | 8.53e-07 | -0.133000 | 7.56e-06 |
| Inwardly rectifying K+ channels | 22 | 2.81e-01 | -0.133000 | 4.64e-01 |
| Regulation of PTEN gene transcription | 59 | 7.81e-02 | -0.133000 | 1.83e-01 |
| Class A/1 (Rhodopsin-like receptors) | 146 | 5.73e-03 | -0.133000 | 2.23e-02 |
| Methylation | 12 | 4.27e-01 | -0.132000 | 6.19e-01 |
| SARS-CoV Infections | 379 | 1.04e-05 | -0.132000 | 7.49e-05 |
| Trafficking and processing of endosomal TLR | 12 | 4.30e-01 | 0.132000 | 6.21e-01 |
| Negative regulators of DDX58/IFIH1 signaling | 34 | 1.85e-01 | -0.132000 | 3.38e-01 |
| Mitochondrial biogenesis | 85 | 3.63e-02 | -0.131000 | 1.06e-01 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 82 | 4.04e-02 | -0.131000 | 1.15e-01 |
| Biosynthesis of DHA-derived SPMs | 11 | 4.53e-01 | 0.131000 | 6.45e-01 |
| IRS-mediated signalling | 35 | 1.82e-01 | -0.130000 | 3.37e-01 |
| RHO GTPases Activate Formins | 126 | 1.18e-02 | -0.130000 | 4.25e-02 |
| Heme biosynthesis | 13 | 4.17e-01 | -0.130000 | 6.09e-01 |
| Role of LAT2/NTAL/LAB on calcium mobilization | 20 | 3.14e-01 | -0.130000 | 4.98e-01 |
| Downstream signaling of activated FGFR4 | 18 | 3.41e-01 | -0.130000 | 5.24e-01 |
| Cell Cycle, Mitotic | 481 | 1.24e-06 | -0.129000 | 1.05e-05 |
| Signaling by TGF-beta Receptor Complex | 90 | 3.41e-02 | -0.129000 | 1.02e-01 |
| Transport of vitamins, nucleosides, and related molecules | 29 | 2.29e-01 | -0.129000 | 3.95e-01 |
| Interleukin-6 signaling | 11 | 4.59e-01 | -0.129000 | 6.50e-01 |
| Synthesis of PC | 23 | 2.85e-01 | -0.129000 | 4.68e-01 |
| Formation of TC-NER Pre-Incision Complex | 53 | 1.05e-01 | -0.129000 | 2.30e-01 |
| Interleukin-17 signaling | 67 | 6.88e-02 | -0.129000 | 1.66e-01 |
| Toll Like Receptor 4 (TLR4) Cascade | 137 | 9.56e-03 | -0.128000 | 3.52e-02 |
| Fcgamma receptor (FCGR) dependent phagocytosis | 90 | 3.54e-02 | -0.128000 | 1.05e-01 |
| mRNA 3’-end processing | 57 | 9.41e-02 | 0.128000 | 2.11e-01 |
| Downstream signal transduction | 28 | 2.41e-01 | -0.128000 | 4.11e-01 |
| EML4 and NUDC in mitotic spindle formation | 103 | 2.56e-02 | -0.127000 | 8.07e-02 |
| Downregulation of ERBB2 signaling | 27 | 2.54e-01 | -0.127000 | 4.30e-01 |
| Adaptive Immune System | 654 | 4.49e-08 | -0.126000 | 5.50e-07 |
| Transport of small molecules | 530 | 7.97e-07 | -0.126000 | 7.15e-06 |
| Heparan sulfate/heparin (HS-GAG) metabolism | 45 | 1.46e-01 | -0.125000 | 2.91e-01 |
| M Phase | 344 | 6.83e-05 | -0.125000 | 4.41e-04 |
| Regulated Necrosis | 51 | 1.23e-01 | -0.125000 | 2.55e-01 |
| Synthesis of bile acids and bile salts | 26 | 2.72e-01 | 0.124000 | 4.52e-01 |
| Synthesis of IP2, IP, and Ins in the cytosol | 12 | 4.56e-01 | 0.124000 | 6.47e-01 |
| Constitutive Signaling by EGFRvIII | 15 | 4.04e-01 | 0.124000 | 5.97e-01 |
| Signaling by EGFRvIII in Cancer | 15 | 4.04e-01 | 0.124000 | 5.97e-01 |
| Signaling by cytosolic FGFR1 fusion mutants | 18 | 3.62e-01 | 0.124000 | 5.52e-01 |
| Neurotransmitter release cycle | 37 | 1.94e-01 | -0.123000 | 3.50e-01 |
| G beta:gamma signalling through CDC42 | 15 | 4.09e-01 | 0.123000 | 6.01e-01 |
| MyD88 dependent cascade initiated on endosome | 101 | 3.30e-02 | -0.123000 | 9.95e-02 |
| Miscellaneous transport and binding events | 21 | 3.30e-01 | -0.123000 | 5.14e-01 |
| SARS-CoV-2 Infection | 265 | 6.24e-04 | -0.122000 | 3.25e-03 |
| Glutamate and glutamine metabolism | 11 | 4.83e-01 | -0.122000 | 6.74e-01 |
| Smooth Muscle Contraction | 37 | 1.99e-01 | -0.122000 | 3.58e-01 |
| Insulin receptor signalling cascade | 40 | 1.84e-01 | -0.121000 | 3.38e-01 |
| Cardiac conduction | 92 | 4.52e-02 | -0.121000 | 1.22e-01 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 100 | 3.71e-02 | -0.121000 | 1.07e-01 |
| Antigen processing: Ubiquitination & Proteasome degradation | 282 | 5.13e-04 | -0.120000 | 2.69e-03 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 32 | 2.39e-01 | 0.120000 | 4.08e-01 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 32 | 2.39e-01 | 0.120000 | 4.08e-01 |
| EGFR downregulation | 27 | 2.80e-01 | -0.120000 | 4.62e-01 |
| Adherens junctions interactions | 44 | 1.68e-01 | -0.120000 | 3.20e-01 |
| MET activates RAS signaling | 11 | 4.90e-01 | 0.120000 | 6.80e-01 |
| FCGR3A-mediated IL10 synthesis | 44 | 1.68e-01 | -0.120000 | 3.20e-01 |
| Signaling by MET | 75 | 7.27e-02 | -0.120000 | 1.74e-01 |
| HCMV Late Events | 59 | 1.16e-01 | -0.118000 | 2.45e-01 |
| Hyaluronan uptake and degradation | 11 | 4.97e-01 | -0.118000 | 6.84e-01 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 27 | 2.88e-01 | -0.118000 | 4.71e-01 |
| Interferon alpha/beta signaling | 57 | 1.24e-01 | -0.118000 | 2.57e-01 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 102 | 4.06e-02 | -0.117000 | 1.15e-01 |
| Sulfur amino acid metabolism | 23 | 3.30e-01 | -0.117000 | 5.14e-01 |
| Regulation of localization of FOXO transcription factors | 12 | 4.82e-01 | -0.117000 | 6.72e-01 |
| Advanced glycosylation endproduct receptor signaling | 12 | 4.82e-01 | -0.117000 | 6.72e-01 |
| MicroRNA (miRNA) biogenesis | 24 | 3.20e-01 | -0.117000 | 5.05e-01 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 17 | 4.04e-01 | -0.117000 | 5.97e-01 |
| Plasma lipoprotein remodeling | 20 | 3.66e-01 | -0.117000 | 5.58e-01 |
| Deubiquitination | 227 | 2.50e-03 | -0.117000 | 1.10e-02 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 22 | 3.44e-01 | -0.117000 | 5.29e-01 |
| Chromosome Maintenance | 92 | 5.41e-02 | -0.116000 | 1.39e-01 |
| Post NMDA receptor activation events | 66 | 1.03e-01 | -0.116000 | 2.27e-01 |
| Cell Cycle | 591 | 1.85e-06 | -0.115000 | 1.51e-05 |
| Heme signaling | 44 | 1.88e-01 | 0.115000 | 3.43e-01 |
| Negative regulation of the PI3K/AKT network | 89 | 6.17e-02 | -0.115000 | 1.52e-01 |
| Circadian Clock | 66 | 1.08e-01 | -0.115000 | 2.33e-01 |
| Sensory perception of sweet, bitter, and umami (glutamate) taste | 13 | 4.75e-01 | 0.115000 | 6.66e-01 |
| SUMOylation of DNA methylation proteins | 16 | 4.30e-01 | -0.114000 | 6.21e-01 |
| Insulin processing | 21 | 3.67e-01 | -0.114000 | 5.58e-01 |
| Eicosanoid ligand-binding receptors | 14 | 4.64e-01 | -0.113000 | 6.54e-01 |
| Intrinsic Pathway for Apoptosis | 52 | 1.59e-01 | -0.113000 | 3.09e-01 |
| The role of Nef in HIV-1 replication and disease pathogenesis | 26 | 3.20e-01 | -0.113000 | 5.04e-01 |
| Prolactin receptor signaling | 11 | 5.19e-01 | 0.112000 | 7.03e-01 |
| Transcriptional regulation of pluripotent stem cells | 16 | 4.38e-01 | -0.112000 | 6.31e-01 |
| Condensation of Prophase Chromosomes | 19 | 4.03e-01 | -0.111000 | 5.96e-01 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 72 | 1.05e-01 | 0.111000 | 2.29e-01 |
| IRAK1 recruits IKK complex | 14 | 4.75e-01 | -0.110000 | 6.66e-01 |
| IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | 14 | 4.75e-01 | -0.110000 | 6.66e-01 |
| Signaling by TGFB family members | 112 | 4.52e-02 | -0.110000 | 1.22e-01 |
| Activation of the AP-1 family of transcription factors | 10 | 5.48e-01 | -0.110000 | 7.25e-01 |
| Voltage gated Potassium channels | 16 | 4.48e-01 | 0.110000 | 6.41e-01 |
| Signaling by Leptin | 10 | 5.51e-01 | -0.109000 | 7.27e-01 |
| Ovarian tumor domain proteases | 35 | 2.66e-01 | -0.109000 | 4.46e-01 |
| mTORC1-mediated signalling | 24 | 3.59e-01 | -0.108000 | 5.48e-01 |
| Signalling to ERKs | 33 | 2.82e-01 | -0.108000 | 4.65e-01 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 56 | 1.62e-01 | -0.108000 | 3.13e-01 |
| ERBB2 Regulates Cell Motility | 13 | 5.02e-01 | 0.108000 | 6.89e-01 |
| Killing mechanisms | 10 | 5.56e-01 | -0.107000 | 7.29e-01 |
| WNT5:FZD7-mediated leishmania damping | 10 | 5.56e-01 | -0.107000 | 7.29e-01 |
| FCERI mediated Ca+2 mobilization | 35 | 2.72e-01 | -0.107000 | 4.52e-01 |
| Nucleotide Excision Repair | 110 | 5.25e-02 | -0.107000 | 1.38e-01 |
| Carnitine metabolism | 13 | 5.06e-01 | 0.107000 | 6.92e-01 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 25 | 3.57e-01 | -0.107000 | 5.45e-01 |
| Resolution of Sister Chromatid Cohesion | 112 | 5.28e-02 | -0.106000 | 1.38e-01 |
| Diseases associated with O-glycosylation of proteins | 55 | 1.74e-01 | 0.106000 | 3.28e-01 |
| NOTCH2 intracellular domain regulates transcription | 10 | 5.62e-01 | 0.106000 | 7.31e-01 |
| Regulation of insulin secretion | 60 | 1.57e-01 | -0.106000 | 3.07e-01 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 24 | 3.70e-01 | -0.106000 | 5.63e-01 |
| Activation of NMDA receptors and postsynaptic events | 78 | 1.07e-01 | -0.106000 | 2.33e-01 |
| Synthesis of very long-chain fatty acyl-CoAs | 18 | 4.41e-01 | -0.105000 | 6.32e-01 |
| Lysosome Vesicle Biogenesis | 33 | 2.97e-01 | -0.105000 | 4.80e-01 |
| RNA Polymerase III Transcription Termination | 23 | 3.84e-01 | -0.105000 | 5.77e-01 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 66 | 1.42e-01 | -0.105000 | 2.85e-01 |
| Signal transduction by L1 | 21 | 4.09e-01 | -0.104000 | 6.00e-01 |
| TP53 Regulates Transcription of Cell Death Genes | 40 | 2.56e-01 | -0.104000 | 4.33e-01 |
| Diseases of signal transduction by growth factor receptors and second messengers | 391 | 4.60e-04 | -0.103000 | 2.45e-03 |
| Metabolism of vitamins and cofactors | 156 | 2.65e-02 | -0.103000 | 8.27e-02 |
| Vesicle-mediated transport | 610 | 1.51e-05 | -0.103000 | 1.07e-04 |
| Class I MHC mediated antigen processing & presentation | 343 | 1.15e-03 | -0.102000 | 5.62e-03 |
| RHOBTB GTPase Cycle | 35 | 2.95e-01 | 0.102000 | 4.77e-01 |
| Extension of Telomeres | 49 | 2.17e-01 | -0.102000 | 3.78e-01 |
| Assembly of the ORC complex at the origin of replication | 14 | 5.09e-01 | -0.102000 | 6.94e-01 |
| Transport of Mature Transcript to Cytoplasm | 81 | 1.13e-01 | 0.102000 | 2.41e-01 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 30 | 3.36e-01 | -0.102000 | 5.19e-01 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | 64 | 1.62e-01 | -0.101000 | 3.13e-01 |
| SUMOylation of SUMOylation proteins | 35 | 3.09e-01 | 0.099300 | 4.94e-01 |
| SUMOylation of ubiquitinylation proteins | 39 | 2.84e-01 | 0.099200 | 4.66e-01 |
| Regulation of TP53 Activity through Phosphorylation | 86 | 1.12e-01 | -0.099200 | 2.39e-01 |
| Translation of Replicase and Assembly of the Replication Transcription Complex 9679504 | 12 | 5.53e-01 | -0.099000 | 7.29e-01 |
| SUMOylation of intracellular receptors | 27 | 3.75e-01 | 0.098700 | 5.67e-01 |
| Toll Like Receptor 9 (TLR9) Cascade | 105 | 8.14e-02 | -0.098500 | 1.89e-01 |
| Intrinsic Pathway of Fibrin Clot Formation | 12 | 5.55e-01 | -0.098500 | 7.29e-01 |
| Presynaptic function of Kainate receptors | 16 | 4.96e-01 | 0.098400 | 6.84e-01 |
| Termination of O-glycan biosynthesis | 14 | 5.25e-01 | -0.098200 | 7.05e-01 |
| Resolution of D-Loop Structures | 33 | 3.30e-01 | 0.098000 | 5.14e-01 |
| Aflatoxin activation and detoxification | 11 | 5.74e-01 | -0.097900 | 7.43e-01 |
| Signal Transduction | 2041 | 1.09e-12 | -0.097000 | 3.33e-11 |
| TP53 Regulates Metabolic Genes | 80 | 1.34e-01 | -0.096800 | 2.75e-01 |
| Transcriptional Regulation by VENTX | 39 | 2.97e-01 | -0.096500 | 4.80e-01 |
| Regulation of innate immune responses to cytosolic DNA | 14 | 5.32e-01 | -0.096400 | 7.12e-01 |
| RHOU GTPase cycle | 39 | 2.99e-01 | 0.096100 | 4.82e-01 |
| Depolymerization of the Nuclear Lamina | 15 | 5.20e-01 | -0.096000 | 7.03e-01 |
| CD209 (DC-SIGN) signaling | 20 | 4.58e-01 | -0.096000 | 6.49e-01 |
| Membrane Trafficking | 575 | 9.15e-05 | -0.095800 | 5.78e-04 |
| RHOQ GTPase cycle | 58 | 2.07e-01 | 0.095800 | 3.67e-01 |
| Formation of Incision Complex in GG-NER | 43 | 2.79e-01 | -0.095500 | 4.60e-01 |
| RHO GTPase Effectors | 245 | 1.01e-02 | -0.095500 | 3.72e-02 |
| GPCR ligand binding | 201 | 1.99e-02 | -0.095400 | 6.52e-02 |
| Early SARS-CoV-2 Infection Events | 33 | 3.49e-01 | -0.094100 | 5.36e-01 |
| MAPK3 (ERK1) activation | 10 | 6.07e-01 | 0.094000 | 7.64e-01 |
| G0 and Early G1 | 25 | 4.16e-01 | -0.094000 | 6.08e-01 |
| Synthesis of glycosylphosphatidylinositol (GPI) | 18 | 4.90e-01 | 0.094000 | 6.80e-01 |
| Biosynthesis of specialized proresolving mediators (SPMs) | 13 | 5.58e-01 | 0.093800 | 7.29e-01 |
| Glutathione conjugation | 29 | 3.82e-01 | -0.093800 | 5.75e-01 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 78 | 1.53e-01 | -0.093500 | 3.03e-01 |
| Signaling by ERBB2 ECD mutants | 16 | 5.18e-01 | 0.093500 | 7.03e-01 |
| HCMV Early Events | 76 | 1.59e-01 | -0.093400 | 3.09e-01 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 56 | 2.27e-01 | -0.093300 | 3.93e-01 |
| Sensory perception of taste | 16 | 5.19e-01 | 0.093200 | 7.03e-01 |
| Synthesis of PIPs at the plasma membrane | 50 | 2.59e-01 | 0.092300 | 4.36e-01 |
| Listeria monocytogenes entry into host cells | 18 | 4.99e-01 | -0.092000 | 6.86e-01 |
| Physiological factors | 10 | 6.15e-01 | -0.092000 | 7.70e-01 |
| Resolution of Abasic Sites (AP sites) | 38 | 3.28e-01 | -0.091700 | 5.13e-01 |
| Anti-inflammatory response favouring Leishmania parasite infection | 75 | 1.72e-01 | -0.091300 | 3.25e-01 |
| Leishmania parasite growth and survival | 75 | 1.72e-01 | -0.091300 | 3.25e-01 |
| Activation of gene expression by SREBF (SREBP) | 42 | 3.11e-01 | -0.090300 | 4.96e-01 |
| G alpha (z) signalling events | 38 | 3.38e-01 | -0.089800 | 5.21e-01 |
| Processing of DNA double-strand break ends | 60 | 2.30e-01 | -0.089600 | 3.96e-01 |
| TP53 Regulates Transcription of Cell Cycle Genes | 44 | 3.05e-01 | -0.089400 | 4.88e-01 |
| Signaling by FLT3 ITD and TKD mutants | 15 | 5.50e-01 | -0.089200 | 7.27e-01 |
| HDACs deacetylate histones | 36 | 3.55e-01 | -0.089100 | 5.44e-01 |
| SUMOylation of DNA damage response and repair proteins | 77 | 1.77e-01 | 0.089000 | 3.30e-01 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 11 | 6.10e-01 | -0.088900 | 7.66e-01 |
| alpha-linolenic acid (ALA) metabolism | 11 | 6.10e-01 | -0.088900 | 7.66e-01 |
| FCGR3A-mediated phagocytosis | 65 | 2.16e-01 | -0.088800 | 3.78e-01 |
| Leishmania phagocytosis | 65 | 2.16e-01 | -0.088800 | 3.78e-01 |
| Parasite infection | 65 | 2.16e-01 | -0.088800 | 3.78e-01 |
| Activation of G protein gated Potassium channels | 19 | 5.04e-01 | -0.088500 | 6.90e-01 |
| G protein gated Potassium channels | 19 | 5.04e-01 | -0.088500 | 6.90e-01 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 19 | 5.04e-01 | -0.088500 | 6.90e-01 |
| HuR (ELAVL1) binds and stabilizes mRNA | 10 | 6.28e-01 | 0.088400 | 7.75e-01 |
| O-linked glycosylation | 86 | 1.58e-01 | -0.088100 | 3.09e-01 |
| G beta:gamma signalling through PI3Kgamma | 20 | 4.96e-01 | 0.088000 | 6.84e-01 |
| SHC1 events in ERBB4 signaling | 12 | 5.98e-01 | -0.088000 | 7.62e-01 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 26 | 4.38e-01 | 0.087900 | 6.31e-01 |
| Metabolism of nitric oxide: NOS3 activation and regulation | 15 | 5.59e-01 | 0.087100 | 7.29e-01 |
| DNA strand elongation | 31 | 4.02e-01 | -0.087000 | 5.96e-01 |
| Signaling by Erythropoietin | 24 | 4.61e-01 | 0.087000 | 6.51e-01 |
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 25 | 4.53e-01 | -0.086800 | 6.45e-01 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | 32 | 3.98e-01 | 0.086300 | 5.92e-01 |
| Rev-mediated nuclear export of HIV RNA | 35 | 3.78e-01 | 0.086200 | 5.71e-01 |
| RNA Polymerase III Transcription Initiation | 36 | 3.72e-01 | -0.085900 | 5.65e-01 |
| Sema4D in semaphorin signaling | 23 | 4.76e-01 | -0.085900 | 6.66e-01 |
| RHOG GTPase cycle | 71 | 2.12e-01 | -0.085800 | 3.73e-01 |
| Cellular hexose transport | 13 | 5.92e-01 | -0.085800 | 7.60e-01 |
| G beta:gamma signalling through BTK | 13 | 5.93e-01 | 0.085700 | 7.60e-01 |
| eNOS activation | 11 | 6.24e-01 | 0.085400 | 7.75e-01 |
| ERBB2 Activates PTK6 Signaling | 11 | 6.24e-01 | 0.085200 | 7.75e-01 |
| Death Receptor Signaling | 147 | 7.60e-02 | -0.084900 | 1.79e-01 |
| Activation of SMO | 16 | 5.58e-01 | -0.084700 | 7.29e-01 |
| Cytosolic sulfonation of small molecules | 19 | 5.26e-01 | -0.084100 | 7.06e-01 |
| RHO GTPases activate PAKs | 20 | 5.17e-01 | -0.083800 | 7.03e-01 |
| PKA activation in glucagon signalling | 16 | 5.62e-01 | -0.083800 | 7.31e-01 |
| Interactions of Vpr with host cellular proteins | 37 | 3.78e-01 | 0.083800 | 5.71e-01 |
| SARS-CoV-2-host interactions | 176 | 5.58e-02 | -0.083700 | 1.42e-01 |
| CRMPs in Sema3A signaling | 15 | 5.76e-01 | -0.083500 | 7.45e-01 |
| Pyroptosis | 21 | 5.08e-01 | -0.083400 | 6.94e-01 |
| Global Genome Nucleotide Excision Repair (GG-NER) | 84 | 1.88e-01 | -0.083200 | 3.43e-01 |
| RND2 GTPase cycle | 36 | 3.89e-01 | 0.082900 | 5.82e-01 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 15 | 5.78e-01 | -0.082900 | 7.46e-01 |
| RND3 GTPase cycle | 36 | 3.91e-01 | 0.082600 | 5.83e-01 |
| MAPK targets/ Nuclear events mediated by MAP kinases | 31 | 4.29e-01 | -0.082100 | 6.21e-01 |
| Impaired BRCA2 binding to PALB2 | 23 | 4.96e-01 | 0.082100 | 6.84e-01 |
| Signaling by FLT3 fusion proteins | 19 | 5.36e-01 | 0.082000 | 7.14e-01 |
| InlB-mediated entry of Listeria monocytogenes into host cell | 14 | 5.97e-01 | -0.081600 | 7.62e-01 |
| Sensory processing of sound by outer hair cells of the cochlea | 35 | 4.06e-01 | 0.081200 | 5.98e-01 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 14 | 6.00e-01 | 0.080900 | 7.64e-01 |
| Neurotransmitter receptors and postsynaptic signal transmission | 142 | 9.72e-02 | -0.080700 | 2.17e-01 |
| Cell-cell junction organization | 63 | 2.68e-01 | -0.080700 | 4.49e-01 |
| Meiosis | 50 | 3.25e-01 | -0.080500 | 5.09e-01 |
| Lagging Strand Synthesis | 20 | 5.33e-01 | 0.080500 | 7.13e-01 |
| CD28 dependent PI3K/Akt signaling | 21 | 5.23e-01 | -0.080500 | 7.05e-01 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | 12 | 6.30e-01 | 0.080300 | 7.75e-01 |
| Branched-chain amino acid catabolism | 21 | 5.24e-01 | 0.080300 | 7.05e-01 |
| Signaling by CSF1 (M-CSF) in myeloid cells | 31 | 4.39e-01 | -0.080300 | 6.32e-01 |
| Transmission across Chemical Synapses | 188 | 5.85e-02 | -0.080100 | 1.47e-01 |
| EPHB-mediated forward signaling | 39 | 3.87e-01 | 0.080100 | 5.80e-01 |
| CREB1 phosphorylation through the activation of Adenylate Cyclase | 11 | 6.46e-01 | 0.079900 | 7.84e-01 |
| Synthesis of PE | 12 | 6.33e-01 | 0.079700 | 7.75e-01 |
| Nucleotide catabolism | 25 | 4.92e-01 | -0.079400 | 6.82e-01 |
| Signal amplification | 27 | 4.76e-01 | -0.079200 | 6.66e-01 |
| Recruitment of NuMA to mitotic centrosomes | 87 | 2.05e-01 | -0.078700 | 3.65e-01 |
| Translation of Replicase and Assembly of the Replication Transcription Complex 9694676 | 13 | 6.25e-01 | -0.078400 | 7.75e-01 |
| Caspase activation via extrinsic apoptotic signalling pathway | 23 | 5.16e-01 | -0.078300 | 7.02e-01 |
| Estrogen-dependent gene expression | 89 | 2.05e-01 | -0.077700 | 3.65e-01 |
| Synthesis of bile acids and bile salts via 24-hydroxycholesterol | 10 | 6.71e-01 | 0.077700 | 7.99e-01 |
| IRAK4 deficiency (TLR2/4) | 15 | 6.03e-01 | 0.077500 | 7.64e-01 |
| SARS-CoV-1 activates/modulates innate immune responses | 39 | 4.04e-01 | -0.077200 | 5.97e-01 |
| Glutathione synthesis and recycling | 10 | 6.73e-01 | -0.077000 | 7.99e-01 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 50 | 3.47e-01 | -0.077000 | 5.32e-01 |
| Cellular response to heat stress | 96 | 1.93e-01 | -0.076900 | 3.50e-01 |
| CD28 co-stimulation | 32 | 4.53e-01 | -0.076700 | 6.45e-01 |
| Platelet homeostasis | 69 | 2.73e-01 | -0.076400 | 4.53e-01 |
| Pre-NOTCH Expression and Processing | 54 | 3.37e-01 | -0.075600 | 5.19e-01 |
| Deposition of new CENPA-containing nucleosomes at the centromere | 30 | 4.74e-01 | -0.075500 | 6.66e-01 |
| Nucleosome assembly | 30 | 4.74e-01 | -0.075500 | 6.66e-01 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | 16 | 6.03e-01 | -0.075100 | 7.64e-01 |
| IKK complex recruitment mediated by RIP1 | 23 | 5.35e-01 | -0.074800 | 7.14e-01 |
| Sphingolipid metabolism | 73 | 2.71e-01 | -0.074500 | 4.52e-01 |
| VxPx cargo-targeting to cilium | 17 | 5.97e-01 | 0.074100 | 7.62e-01 |
| Opioid Signalling | 79 | 2.59e-01 | -0.073600 | 4.36e-01 |
| Toll-like Receptor Cascades | 157 | 1.13e-01 | -0.073400 | 2.40e-01 |
| PRC2 methylates histones and DNA | 19 | 5.84e-01 | -0.072600 | 7.52e-01 |
| G alpha (12/13) signalling events | 70 | 2.94e-01 | 0.072500 | 4.77e-01 |
| Processing of SMDT1 | 15 | 6.27e-01 | -0.072400 | 7.75e-01 |
| Interleukin-2 family signaling | 36 | 4.52e-01 | -0.072400 | 6.45e-01 |
| Phase II - Conjugation of compounds | 69 | 3.00e-01 | -0.072200 | 4.83e-01 |
| Signaling by ERBB2 in Cancer | 24 | 5.41e-01 | 0.072100 | 7.18e-01 |
| Mucopolysaccharidoses | 11 | 6.79e-01 | 0.072100 | 8.02e-01 |
| Signaling by Non-Receptor Tyrosine Kinases | 51 | 3.74e-01 | -0.072000 | 5.66e-01 |
| Signaling by PTK6 | 51 | 3.74e-01 | -0.072000 | 5.66e-01 |
| Nuclear import of Rev protein | 34 | 4.70e-01 | 0.071600 | 6.62e-01 |
| LDL clearance | 17 | 6.12e-01 | 0.071000 | 7.68e-01 |
| Meiotic synapsis | 31 | 4.94e-01 | -0.071000 | 6.84e-01 |
| Integrin signaling | 23 | 5.56e-01 | -0.070900 | 7.29e-01 |
| Peroxisomal protein import | 57 | 3.56e-01 | 0.070700 | 5.45e-01 |
| Caspase activation via Death Receptors in the presence of ligand | 15 | 6.36e-01 | -0.070600 | 7.77e-01 |
| RND1 GTPase cycle | 37 | 4.59e-01 | 0.070300 | 6.50e-01 |
| Energy dependent regulation of mTOR by LKB1-AMPK | 28 | 5.21e-01 | 0.070100 | 7.04e-01 |
| Epigenetic regulation of gene expression | 133 | 1.64e-01 | 0.070000 | 3.15e-01 |
| RHOC GTPase cycle | 70 | 3.12e-01 | 0.069900 | 4.96e-01 |
| FRS-mediated FGFR1 signaling | 15 | 6.41e-01 | -0.069600 | 7.81e-01 |
| SUMOylation of transcription cofactors | 44 | 4.25e-01 | -0.069500 | 6.18e-01 |
| FGFR1 mutant receptor activation | 25 | 5.48e-01 | -0.069500 | 7.25e-01 |
| Phospholipid metabolism | 177 | 1.11e-01 | 0.069500 | 2.38e-01 |
| Neuronal System | 263 | 5.30e-02 | -0.069400 | 1.38e-01 |
| Ion channel transport | 133 | 1.69e-01 | -0.069100 | 3.22e-01 |
| DNA Repair | 280 | 4.73e-02 | -0.069000 | 1.27e-01 |
| Prostacyclin signalling through prostacyclin receptor | 14 | 6.55e-01 | -0.069000 | 7.90e-01 |
| FOXO-mediated transcription of cell cycle genes | 15 | 6.45e-01 | -0.068700 | 7.84e-01 |
| Deadenylation of mRNA | 22 | 5.77e-01 | 0.068700 | 7.46e-01 |
| RAC1 GTPase cycle | 173 | 1.20e-01 | 0.068500 | 2.51e-01 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 87 | 2.72e-01 | -0.068200 | 4.52e-01 |
| Amplification of signal from the kinetochores | 87 | 2.72e-01 | -0.068200 | 4.52e-01 |
| Gap junction degradation | 12 | 6.83e-01 | -0.068200 | 8.03e-01 |
| BBSome-mediated cargo-targeting to cilium | 21 | 5.89e-01 | -0.068100 | 7.57e-01 |
| PCNA-Dependent Long Patch Base Excision Repair | 21 | 5.92e-01 | -0.067500 | 7.60e-01 |
| Activation of RAC1 | 11 | 6.99e-01 | 0.067400 | 8.16e-01 |
| Adenylate cyclase inhibitory pathway | 13 | 6.77e-01 | 0.066800 | 8.01e-01 |
| PI3K events in ERBB2 signaling | 14 | 6.66e-01 | 0.066700 | 7.98e-01 |
| Homologous DNA Pairing and Strand Exchange | 41 | 4.63e-01 | 0.066200 | 6.54e-01 |
| Nonhomologous End-Joining (NHEJ) | 34 | 5.05e-01 | 0.066100 | 6.90e-01 |
| Removal of the Flap Intermediate | 14 | 6.70e-01 | 0.065800 | 7.99e-01 |
| HDMs demethylate histones | 21 | 6.03e-01 | -0.065600 | 7.64e-01 |
| FLT3 Signaling | 36 | 4.97e-01 | -0.065400 | 6.84e-01 |
| Cell-extracellular matrix interactions | 18 | 6.36e-01 | -0.064500 | 7.77e-01 |
| Signal regulatory protein family interactions | 11 | 7.12e-01 | 0.064400 | 8.26e-01 |
| Regulation of KIT signaling | 16 | 6.57e-01 | -0.064100 | 7.92e-01 |
| Metabolism of non-coding RNA | 53 | 4.20e-01 | 0.064000 | 6.12e-01 |
| snRNP Assembly | 53 | 4.20e-01 | 0.064000 | 6.12e-01 |
| Signaling by EGFR | 46 | 4.55e-01 | -0.063700 | 6.47e-01 |
| FCERI mediated MAPK activation | 36 | 5.08e-01 | -0.063700 | 6.94e-01 |
| Biotin transport and metabolism | 11 | 7.15e-01 | -0.063600 | 8.28e-01 |
| Other semaphorin interactions | 19 | 6.33e-01 | -0.063300 | 7.75e-01 |
| Leishmania infection | 155 | 1.75e-01 | -0.063200 | 3.28e-01 |
| Parasitic Infection Pathways | 155 | 1.75e-01 | -0.063200 | 3.28e-01 |
| RET signaling | 33 | 5.33e-01 | -0.062700 | 7.13e-01 |
| EPHA-mediated growth cone collapse | 22 | 6.11e-01 | -0.062600 | 7.68e-01 |
| Antiviral mechanism by IFN-stimulated genes | 79 | 3.37e-01 | 0.062600 | 5.19e-01 |
| Regulation of FOXO transcriptional activity by acetylation | 10 | 7.33e-01 | 0.062400 | 8.41e-01 |
| E2F mediated regulation of DNA replication | 21 | 6.21e-01 | 0.062400 | 7.75e-01 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 32 | 5.43e-01 | -0.062100 | 7.20e-01 |
| Mitotic Prophase | 88 | 3.14e-01 | -0.062100 | 4.98e-01 |
| Golgi Associated Vesicle Biogenesis | 55 | 4.26e-01 | -0.062000 | 6.19e-01 |
| Signaling by GPCR | 406 | 3.33e-02 | -0.061700 | 1.00e-01 |
| Mitochondrial Fatty Acid Beta-Oxidation | 34 | 5.35e-01 | -0.061400 | 7.14e-01 |
| Cell junction organization | 88 | 3.20e-01 | -0.061400 | 5.04e-01 |
| rRNA processing in the mitochondrion | 10 | 7.37e-01 | -0.061300 | 8.44e-01 |
| Apoptotic factor-mediated response | 20 | 6.38e-01 | 0.060800 | 7.78e-01 |
| Activation of HOX genes during differentiation | 65 | 3.98e-01 | -0.060700 | 5.91e-01 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 65 | 3.98e-01 | -0.060700 | 5.91e-01 |
| Activation of the pre-replicative complex | 29 | 5.72e-01 | -0.060600 | 7.42e-01 |
| CDC42 GTPase cycle | 146 | 2.08e-01 | 0.060400 | 3.68e-01 |
| NCAM signaling for neurite out-growth | 53 | 4.51e-01 | -0.059900 | 6.45e-01 |
| GPCR downstream signalling | 365 | 5.15e-02 | -0.059500 | 1.35e-01 |
| Interleukin receptor SHC signaling | 22 | 6.30e-01 | -0.059400 | 7.75e-01 |
| Semaphorin interactions | 62 | 4.21e-01 | -0.059200 | 6.12e-01 |
| Mitotic Spindle Checkpoint | 104 | 2.98e-01 | -0.059100 | 4.80e-01 |
| Glucagon signaling in metabolic regulation | 26 | 6.04e-01 | -0.058700 | 7.64e-01 |
| Metabolism of water-soluble vitamins and cofactors | 108 | 2.93e-01 | -0.058600 | 4.76e-01 |
| Interleukin-37 signaling | 20 | 6.50e-01 | 0.058600 | 7.87e-01 |
| RHO GTPases Activate ROCKs | 18 | 6.68e-01 | -0.058500 | 7.99e-01 |
| Extra-nuclear estrogen signaling | 66 | 4.13e-01 | -0.058300 | 6.05e-01 |
| Tryptophan catabolism | 10 | 7.50e-01 | 0.058300 | 8.52e-01 |
| Adrenaline,noradrenaline inhibits insulin secretion | 23 | 6.29e-01 | -0.058100 | 7.75e-01 |
| Intra-Golgi traffic | 42 | 5.18e-01 | -0.057700 | 7.03e-01 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 25 | 6.19e-01 | -0.057400 | 7.74e-01 |
| RHO GTPases activate KTN1 | 10 | 7.54e-01 | 0.057100 | 8.55e-01 |
| Regulation of Expression and Function of Type II Classical Cadherins | 29 | 5.95e-01 | -0.057000 | 7.60e-01 |
| Regulation of Homotypic Cell-Cell Adhesion | 29 | 5.95e-01 | -0.057000 | 7.60e-01 |
| SHC1 events in ERBB2 signaling | 20 | 6.60e-01 | -0.056900 | 7.93e-01 |
| Metabolism of steroids | 120 | 2.84e-01 | -0.056700 | 4.66e-01 |
| Aspirin ADME | 14 | 7.14e-01 | -0.056600 | 8.27e-01 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | 24 | 6.31e-01 | 0.056600 | 7.75e-01 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | 24 | 6.31e-01 | 0.056600 | 7.75e-01 |
| Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 24 | 6.31e-01 | 0.056600 | 7.75e-01 |
| Defective homologous recombination repair (HRR) due to PALB2 loss of function | 24 | 6.31e-01 | 0.056600 | 7.75e-01 |
| mRNA Splicing - Major Pathway | 202 | 1.67e-01 | -0.056400 | 3.20e-01 |
| Effects of PIP2 hydrolysis | 22 | 6.47e-01 | -0.056400 | 7.84e-01 |
| Scavenging by Class A Receptors | 16 | 6.97e-01 | -0.056200 | 8.16e-01 |
| CD28 dependent Vav1 pathway | 11 | 7.47e-01 | 0.056100 | 8.50e-01 |
| Early Phase of HIV Life Cycle | 14 | 7.18e-01 | -0.055700 | 8.30e-01 |
| Plasma lipoprotein assembly, remodeling, and clearance | 56 | 4.71e-01 | -0.055700 | 6.63e-01 |
| EPH-ephrin mediated repulsion of cells | 44 | 5.23e-01 | -0.055700 | 7.05e-01 |
| Myogenesis | 21 | 6.59e-01 | -0.055600 | 7.93e-01 |
| RHOB GTPase cycle | 66 | 4.40e-01 | 0.055000 | 6.32e-01 |
| Formation of definitive endoderm | 10 | 7.65e-01 | 0.054700 | 8.63e-01 |
| ESR-mediated signaling | 152 | 2.46e-01 | -0.054600 | 4.19e-01 |
| Maturation of nucleoprotein 9683610 | 11 | 7.54e-01 | 0.054600 | 8.55e-01 |
| Defects in vitamin and cofactor metabolism | 20 | 6.74e-01 | 0.054400 | 7.99e-01 |
| Stimuli-sensing channels | 72 | 4.26e-01 | 0.054300 | 6.18e-01 |
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 39 | 5.58e-01 | 0.054300 | 7.29e-01 |
| Diseases of DNA Double-Strand Break Repair | 39 | 5.58e-01 | 0.054300 | 7.29e-01 |
| SIRT1 negatively regulates rRNA expression | 14 | 7.25e-01 | 0.054300 | 8.36e-01 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 19 | 6.83e-01 | -0.054200 | 8.03e-01 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 19 | 6.83e-01 | -0.054200 | 8.03e-01 |
| Regulation of HSF1-mediated heat shock response | 78 | 4.11e-01 | -0.053900 | 6.03e-01 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 37 | 5.73e-01 | -0.053600 | 7.42e-01 |
| NOD1/2 Signaling Pathway | 36 | 5.80e-01 | -0.053300 | 7.48e-01 |
| G1/S-Specific Transcription | 25 | 6.45e-01 | -0.053300 | 7.84e-01 |
| ERK/MAPK targets | 22 | 6.66e-01 | -0.053100 | 7.98e-01 |
| Downstream signaling of activated FGFR1 | 21 | 6.74e-01 | -0.053000 | 7.99e-01 |
| Metabolism of porphyrins | 21 | 6.74e-01 | -0.053000 | 7.99e-01 |
| Sensory processing of sound by inner hair cells of the cochlea | 49 | 5.22e-01 | -0.052900 | 7.04e-01 |
| Transport of inorganic cations/anions and amino acids/oligopeptides | 66 | 4.57e-01 | -0.052900 | 6.49e-01 |
| Ion transport by P-type ATPases | 42 | 5.53e-01 | -0.052900 | 7.29e-01 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 39 | 5.69e-01 | -0.052700 | 7.39e-01 |
| Activation of kainate receptors upon glutamate binding | 23 | 6.63e-01 | -0.052500 | 7.96e-01 |
| Regulation of MECP2 expression and activity | 29 | 6.32e-01 | 0.051400 | 7.75e-01 |
| PKA-mediated phosphorylation of CREB | 19 | 6.99e-01 | 0.051300 | 8.16e-01 |
| DAP12 signaling | 27 | 6.48e-01 | 0.050800 | 7.84e-01 |
| Interactions of Rev with host cellular proteins | 37 | 5.95e-01 | 0.050500 | 7.60e-01 |
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) | 14 | 7.43e-01 | -0.050500 | 8.49e-01 |
| Activation of ATR in response to replication stress | 31 | 6.27e-01 | -0.050400 | 7.75e-01 |
| Ephrin signaling | 18 | 7.12e-01 | 0.050300 | 8.26e-01 |
| Triglyceride catabolism | 16 | 7.33e-01 | -0.049200 | 8.41e-01 |
| Signaling by ERBB2 | 47 | 5.60e-01 | -0.049100 | 7.30e-01 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | 21 | 7.00e-01 | -0.048600 | 8.16e-01 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 21 | 7.00e-01 | -0.048600 | 8.16e-01 |
| Metabolism of steroid hormones | 21 | 7.02e-01 | -0.048200 | 8.18e-01 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 17 | 7.31e-01 | 0.048200 | 8.40e-01 |
| RHOD GTPase cycle | 50 | 5.58e-01 | 0.047900 | 7.29e-01 |
| HDR through Single Strand Annealing (SSA) | 35 | 6.25e-01 | 0.047700 | 7.75e-01 |
| CaM pathway | 32 | 6.42e-01 | 0.047500 | 7.81e-01 |
| Calmodulin induced events | 32 | 6.42e-01 | 0.047500 | 7.81e-01 |
| Signaling by BMP | 23 | 6.95e-01 | 0.047200 | 8.16e-01 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | 101 | 4.13e-01 | 0.047200 | 6.05e-01 |
| Synthesis of PA | 29 | 6.61e-01 | 0.047000 | 7.95e-01 |
| RNA polymerase II transcribes snRNA genes | 71 | 4.94e-01 | -0.046900 | 6.84e-01 |
| DAP12 interactions | 35 | 6.34e-01 | -0.046500 | 7.76e-01 |
| Dual incision in TC-NER | 65 | 5.18e-01 | -0.046400 | 7.03e-01 |
| RHOBTB2 GTPase cycle | 23 | 7.01e-01 | -0.046200 | 8.17e-01 |
| Signaling by NTRK2 (TRKB) | 22 | 7.08e-01 | 0.046100 | 8.23e-01 |
| Glycogen breakdown (glycogenolysis) | 13 | 7.75e-01 | -0.045700 | 8.70e-01 |
| RNA Polymerase I Promoter Escape | 37 | 6.30e-01 | -0.045700 | 7.75e-01 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 28 | 6.75e-01 | -0.045700 | 8.00e-01 |
| SHC1 events in EGFR signaling | 11 | 7.93e-01 | 0.045600 | 8.80e-01 |
| Regulated proteolysis of p75NTR | 11 | 7.94e-01 | -0.045500 | 8.80e-01 |
| Vitamin B5 (pantothenate) metabolism | 16 | 7.53e-01 | -0.045500 | 8.54e-01 |
| HDR through Homologous Recombination (HRR) | 65 | 5.28e-01 | 0.045300 | 7.08e-01 |
| p75 NTR receptor-mediated signalling | 91 | 4.60e-01 | -0.044800 | 6.51e-01 |
| mRNA Splicing | 210 | 2.67e-01 | -0.044500 | 4.48e-01 |
| DNA Double-Strand Break Repair | 129 | 3.86e-01 | -0.044300 | 5.79e-01 |
| trans-Golgi Network Vesicle Budding | 70 | 5.24e-01 | -0.044000 | 7.05e-01 |
| Transcriptional regulation of white adipocyte differentiation | 81 | 4.96e-01 | -0.043700 | 6.84e-01 |
| NRAGE signals death through JNK | 56 | 5.72e-01 | 0.043700 | 7.42e-01 |
| ISG15 antiviral mechanism | 71 | 5.26e-01 | 0.043500 | 7.06e-01 |
| ALK mutants bind TKIs | 12 | 7.95e-01 | -0.043300 | 8.81e-01 |
| Erythropoietin activates RAS | 13 | 7.88e-01 | -0.043200 | 8.78e-01 |
| Ca2+ pathway | 54 | 5.85e-01 | 0.042900 | 7.53e-01 |
| Intraflagellar transport | 49 | 6.04e-01 | -0.042900 | 7.64e-01 |
| Impaired BRCA2 binding to RAD51 | 33 | 6.71e-01 | 0.042700 | 7.99e-01 |
| Signaling by NOTCH2 | 31 | 6.82e-01 | -0.042600 | 8.03e-01 |
| Reproduction | 67 | 5.48e-01 | -0.042500 | 7.25e-01 |
| Signaling by ERBB2 KD Mutants | 23 | 7.25e-01 | 0.042400 | 8.36e-01 |
| Nuclear Envelope Breakdown | 53 | 5.98e-01 | 0.041900 | 7.62e-01 |
| Transcriptional Regulation by MECP2 | 48 | 6.18e-01 | -0.041600 | 7.74e-01 |
| Mitotic Prometaphase | 188 | 3.28e-01 | -0.041400 | 5.13e-01 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | 12 | 8.04e-01 | 0.041300 | 8.86e-01 |
| Processive synthesis on the lagging strand | 15 | 7.83e-01 | 0.041100 | 8.74e-01 |
| PLC beta mediated events | 46 | 6.30e-01 | 0.041100 | 7.75e-01 |
| tRNA processing in the nucleus | 59 | 5.91e-01 | 0.040500 | 7.59e-01 |
| Homology Directed Repair | 100 | 4.85e-01 | -0.040500 | 6.75e-01 |
| Netrin-1 signaling | 41 | 6.55e-01 | 0.040300 | 7.90e-01 |
| Triglyceride metabolism | 24 | 7.34e-01 | -0.040100 | 8.41e-01 |
| Tie2 Signaling | 15 | 7.90e-01 | -0.039700 | 8.80e-01 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 57 | 6.06e-01 | 0.039500 | 7.64e-01 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 57 | 6.06e-01 | 0.039500 | 7.64e-01 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 57 | 6.06e-01 | 0.039500 | 7.64e-01 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 57 | 6.06e-01 | 0.039500 | 7.64e-01 |
| Signaling by NOTCH1 in Cancer | 57 | 6.06e-01 | 0.039500 | 7.64e-01 |
| HDR through MMEJ (alt-NHEJ) | 12 | 8.13e-01 | 0.039400 | 8.90e-01 |
| Polymerase switching on the C-strand of the telomere | 26 | 7.28e-01 | 0.039400 | 8.38e-01 |
| Transcriptional Regulation by E2F6 | 34 | 6.91e-01 | 0.039400 | 8.12e-01 |
| LGI-ADAM interactions | 10 | 8.30e-01 | 0.039300 | 8.97e-01 |
| Deadenylation-dependent mRNA decay | 50 | 6.32e-01 | -0.039200 | 7.75e-01 |
| Regulation of lipid metabolism by PPARalpha | 106 | 4.89e-01 | 0.038900 | 6.80e-01 |
| Presynaptic phase of homologous DNA pairing and strand exchange | 38 | 6.78e-01 | 0.038900 | 8.02e-01 |
| Class B/2 (Secretin family receptors) | 51 | 6.33e-01 | -0.038700 | 7.75e-01 |
| RNA Polymerase III Abortive And Retractive Initiation | 41 | 6.69e-01 | -0.038600 | 7.99e-01 |
| RNA Polymerase III Transcription | 41 | 6.69e-01 | -0.038600 | 7.99e-01 |
| Regulation of beta-cell development | 19 | 7.73e-01 | 0.038200 | 8.70e-01 |
| Mitochondrial calcium ion transport | 21 | 7.62e-01 | -0.038200 | 8.61e-01 |
| Cargo recognition for clathrin-mediated endocytosis | 91 | 5.40e-01 | -0.037200 | 7.18e-01 |
| Hyaluronan metabolism | 16 | 8.00e-01 | -0.036500 | 8.84e-01 |
| Potassium Channels | 52 | 6.51e-01 | -0.036300 | 7.87e-01 |
| FOXO-mediated transcription | 57 | 6.37e-01 | -0.036100 | 7.78e-01 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 31 | 7.28e-01 | -0.036100 | 8.38e-01 |
| Phase 0 - rapid depolarisation | 23 | 7.65e-01 | -0.036000 | 8.63e-01 |
| Signaling by Rho GTPases | 599 | 1.38e-01 | -0.035600 | 2.80e-01 |
| Fanconi Anemia Pathway | 35 | 7.16e-01 | 0.035600 | 8.28e-01 |
| Clathrin-mediated endocytosis | 130 | 4.84e-01 | -0.035600 | 6.74e-01 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 12 | 8.33e-01 | -0.035300 | 8.99e-01 |
| PPARA activates gene expression | 104 | 5.36e-01 | 0.035100 | 7.14e-01 |
| Regulation of PLK1 Activity at G2/M Transition | 85 | 5.77e-01 | -0.035000 | 7.46e-01 |
| RNA Polymerase II Transcription Termination | 66 | 6.25e-01 | 0.034800 | 7.75e-01 |
| mRNA decay by 3’ to 5’ exoribonuclease | 13 | 8.28e-01 | -0.034700 | 8.96e-01 |
| Negative regulation of MET activity | 20 | 7.88e-01 | -0.034700 | 8.78e-01 |
| Cell-Cell communication | 116 | 5.20e-01 | -0.034600 | 7.03e-01 |
| Signaling by Rho GTPases, Miro GTPases and RHOBTB3 | 614 | 1.46e-01 | -0.034500 | 2.91e-01 |
| RHOJ GTPase cycle | 53 | 6.67e-01 | 0.034200 | 7.98e-01 |
| Prolonged ERK activation events | 14 | 8.26e-01 | 0.034000 | 8.95e-01 |
| Retrograde transport at the Trans-Golgi-Network | 49 | 6.82e-01 | -0.033900 | 8.03e-01 |
| PECAM1 interactions | 12 | 8.40e-01 | -0.033700 | 9.03e-01 |
| Frs2-mediated activation | 12 | 8.40e-01 | 0.033600 | 9.03e-01 |
| GPVI-mediated activation cascade | 32 | 7.43e-01 | -0.033400 | 8.49e-01 |
| Signaling by EGFR in Cancer | 22 | 7.87e-01 | -0.033300 | 8.78e-01 |
| Gene Silencing by RNA | 78 | 6.12e-01 | 0.033200 | 7.68e-01 |
| Sphingolipid de novo biosynthesis | 37 | 7.27e-01 | 0.033100 | 8.38e-01 |
| Signaling by NOTCH3 | 46 | 6.98e-01 | -0.033100 | 8.16e-01 |
| Cell recruitment (pro-inflammatory response) | 24 | 7.80e-01 | -0.032900 | 8.73e-01 |
| Purinergic signaling in leishmaniasis infection | 24 | 7.80e-01 | -0.032900 | 8.73e-01 |
| Cytochrome P450 - arranged by substrate type | 32 | 7.48e-01 | 0.032900 | 8.50e-01 |
| RHO GTPases Activate WASPs and WAVEs | 35 | 7.39e-01 | -0.032600 | 8.46e-01 |
| FLT3 signaling in disease | 27 | 7.72e-01 | -0.032200 | 8.70e-01 |
| RHO GTPases activate CIT | 18 | 8.15e-01 | -0.031900 | 8.90e-01 |
| Postmitotic nuclear pore complex (NPC) reformation | 27 | 7.75e-01 | -0.031700 | 8.70e-01 |
| Endogenous sterols | 20 | 8.08e-01 | -0.031500 | 8.87e-01 |
| Phase I - Functionalization of compounds | 65 | 6.63e-01 | 0.031200 | 7.96e-01 |
| ADORA2B mediated anti-inflammatory cytokines production | 36 | 7.47e-01 | -0.031100 | 8.50e-01 |
| TBC/RABGAPs | 44 | 7.22e-01 | -0.031000 | 8.34e-01 |
| Ca-dependent events | 34 | 7.56e-01 | 0.030900 | 8.55e-01 |
| Nuclear signaling by ERBB4 | 28 | 7.78e-01 | 0.030800 | 8.72e-01 |
| TRAF6 mediated NF-kB activation | 23 | 7.98e-01 | 0.030800 | 8.83e-01 |
| IRF3-mediated induction of type I IFN | 12 | 8.54e-01 | 0.030700 | 9.10e-01 |
| Phosphorylation of the APC/C | 20 | 8.14e-01 | -0.030400 | 8.90e-01 |
| Thromboxane signalling through TP receptor | 19 | 8.19e-01 | -0.030300 | 8.92e-01 |
| Telomere C-strand (Lagging Strand) Synthesis | 34 | 7.60e-01 | -0.030200 | 8.60e-01 |
| G-protein activation | 18 | 8.26e-01 | 0.029900 | 8.95e-01 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 19 | 8.22e-01 | 0.029700 | 8.93e-01 |
| Organelle biogenesis and maintenance | 271 | 4.07e-01 | -0.029300 | 5.99e-01 |
| PKA activation | 17 | 8.35e-01 | -0.029100 | 9.01e-01 |
| Biological oxidations | 138 | 5.57e-01 | -0.029000 | 7.29e-01 |
| G alpha (s) signalling events | 85 | 6.47e-01 | -0.028700 | 7.84e-01 |
| Glyoxylate metabolism and glycine degradation | 23 | 8.12e-01 | -0.028700 | 8.90e-01 |
| Regulation of TLR by endogenous ligand | 15 | 8.48e-01 | 0.028500 | 9.07e-01 |
| Visual phototransduction | 58 | 7.13e-01 | -0.027900 | 8.27e-01 |
| Class I peroxisomal membrane protein import | 19 | 8.34e-01 | -0.027800 | 9.00e-01 |
| EPH-Ephrin signaling | 82 | 6.73e-01 | -0.026900 | 7.99e-01 |
| Anchoring of the basal body to the plasma membrane | 95 | 6.59e-01 | 0.026200 | 7.93e-01 |
| SLC transporter disorders | 70 | 7.05e-01 | 0.026100 | 8.21e-01 |
| Transcriptional regulation by small RNAs | 53 | 7.45e-01 | -0.025900 | 8.49e-01 |
| RAC2 GTPase cycle | 85 | 6.83e-01 | 0.025600 | 8.04e-01 |
| GRB2 events in ERBB2 signaling | 14 | 8.68e-01 | 0.025600 | 9.24e-01 |
| Interaction between L1 and Ankyrins | 25 | 8.25e-01 | -0.025500 | 8.95e-01 |
| Laminin interactions | 27 | 8.19e-01 | -0.025500 | 8.92e-01 |
| Activation of GABAB receptors | 32 | 8.03e-01 | -0.025400 | 8.86e-01 |
| GABA B receptor activation | 32 | 8.03e-01 | -0.025400 | 8.86e-01 |
| RHO GTPases activate PKNs | 36 | 7.93e-01 | -0.025300 | 8.80e-01 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 21 | 8.41e-01 | -0.025300 | 9.03e-01 |
| PI-3K cascade:FGFR1 | 13 | 8.78e-01 | -0.024500 | 9.28e-01 |
| RHO GTPase cycle | 419 | 3.91e-01 | 0.024500 | 5.83e-01 |
| Signaling by Nuclear Receptors | 214 | 5.41e-01 | -0.024300 | 7.18e-01 |
| NOTCH1 Intracellular Domain Regulates Transcription | 47 | 7.74e-01 | -0.024200 | 8.70e-01 |
| Diseases of DNA repair | 48 | 7.72e-01 | 0.024200 | 8.70e-01 |
| MyD88 deficiency (TLR2/4) | 14 | 8.76e-01 | 0.024100 | 9.27e-01 |
| Pre-NOTCH Transcription and Translation | 38 | 7.99e-01 | 0.023900 | 8.83e-01 |
| G-protein mediated events | 50 | 7.73e-01 | 0.023600 | 8.70e-01 |
| SUMO E3 ligases SUMOylate target proteins | 162 | 6.04e-01 | 0.023600 | 7.64e-01 |
| ADP signalling through P2Y purinoceptor 12 | 16 | 8.70e-01 | 0.023600 | 9.25e-01 |
| Signaling by high-kinase activity BRAF mutants | 31 | 8.21e-01 | 0.023500 | 8.93e-01 |
| Maturation of nucleoprotein 9694631 | 15 | 8.75e-01 | -0.023500 | 9.26e-01 |
| B-WICH complex positively regulates rRNA expression | 37 | 8.06e-01 | 0.023300 | 8.87e-01 |
| MAP2K and MAPK activation | 35 | 8.11e-01 | 0.023300 | 8.90e-01 |
| Sensory Perception | 148 | 6.28e-01 | 0.023100 | 7.75e-01 |
| ADP signalling through P2Y purinoceptor 1 | 20 | 8.58e-01 | -0.023100 | 9.14e-01 |
| Vasopressin regulates renal water homeostasis via Aquaporins | 34 | 8.18e-01 | 0.022800 | 8.92e-01 |
| Positive epigenetic regulation of rRNA expression | 52 | 7.76e-01 | -0.022800 | 8.70e-01 |
| NOTCH3 Intracellular Domain Regulates Transcription | 22 | 8.54e-01 | 0.022700 | 9.10e-01 |
| Signaling by NOTCH1 | 72 | 7.42e-01 | 0.022500 | 8.49e-01 |
| Sensory processing of sound | 52 | 7.82e-01 | -0.022200 | 8.74e-01 |
| Inositol phosphate metabolism | 42 | 8.05e-01 | -0.022100 | 8.86e-01 |
| VEGFR2 mediated vascular permeability | 27 | 8.45e-01 | 0.021700 | 9.06e-01 |
| DNA Damage Bypass | 46 | 8.02e-01 | 0.021400 | 8.85e-01 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | 12 | 8.99e-01 | 0.021200 | 9.46e-01 |
| Arachidonic acid metabolism | 36 | 8.25e-01 | 0.021200 | 8.95e-01 |
| Cargo trafficking to the periciliary membrane | 45 | 8.07e-01 | 0.021000 | 8.87e-01 |
| Defective B3GALTL causes PpS | 34 | 8.38e-01 | 0.020300 | 9.02e-01 |
| G2/M DNA damage checkpoint | 57 | 7.93e-01 | -0.020100 | 8.80e-01 |
| p130Cas linkage to MAPK signaling for integrins | 12 | 9.05e-01 | -0.019900 | 9.49e-01 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 94 | 7.44e-01 | -0.019500 | 8.49e-01 |
| Transcriptional activation of mitochondrial biogenesis | 49 | 8.17e-01 | -0.019100 | 8.92e-01 |
| SUMOylation of chromatin organization proteins | 57 | 8.09e-01 | 0.018600 | 8.88e-01 |
| Germ layer formation at gastrulation | 11 | 9.17e-01 | 0.018200 | 9.54e-01 |
| Signaling by PDGFR in disease | 20 | 8.88e-01 | -0.018200 | 9.35e-01 |
| Glycerophospholipid biosynthesis | 100 | 7.55e-01 | -0.018000 | 8.55e-01 |
| Cilium Assembly | 186 | 6.74e-01 | 0.017900 | 7.99e-01 |
| Oncogenic MAPK signaling | 74 | 7.92e-01 | 0.017700 | 8.80e-01 |
| Viral Messenger RNA Synthesis | 44 | 8.39e-01 | -0.017700 | 9.03e-01 |
| Drug ADME | 58 | 8.18e-01 | -0.017500 | 8.92e-01 |
| DAG and IP3 signaling | 38 | 8.53e-01 | -0.017300 | 9.10e-01 |
| SUMOylation of transcription factors | 17 | 9.02e-01 | 0.017200 | 9.48e-01 |
| Nephrin family interactions | 18 | 8.99e-01 | -0.017200 | 9.46e-01 |
| Interferon Signaling | 166 | 7.07e-01 | -0.016900 | 8.22e-01 |
| Sema3A PAK dependent Axon repulsion | 16 | 9.07e-01 | -0.016900 | 9.49e-01 |
| Constitutive Signaling by Overexpressed ERBB2 | 11 | 9.25e-01 | 0.016300 | 9.59e-01 |
| Diseases associated with the TLR signaling cascade | 27 | 8.85e-01 | 0.016100 | 9.33e-01 |
| Diseases of Immune System | 27 | 8.85e-01 | 0.016100 | 9.33e-01 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 13 | 9.21e-01 | 0.015900 | 9.56e-01 |
| Chromatin modifying enzymes | 203 | 6.97e-01 | -0.015900 | 8.16e-01 |
| Chromatin organization | 203 | 6.97e-01 | -0.015900 | 8.16e-01 |
| RHOH GTPase cycle | 32 | 8.77e-01 | 0.015800 | 9.27e-01 |
| Gene expression (Transcription) | 1357 | 3.34e-01 | 0.015800 | 5.18e-01 |
| mitochondrial fatty acid beta-oxidation of saturated fatty acids | 10 | 9.34e-01 | 0.015200 | 9.64e-01 |
| Tight junction interactions | 17 | 9.14e-01 | 0.015200 | 9.53e-01 |
| Nuclear Receptor transcription pathway | 40 | 8.71e-01 | -0.014800 | 9.25e-01 |
| RNA Polymerase I Promoter Clearance | 56 | 8.49e-01 | -0.014700 | 9.07e-01 |
| RNA Polymerase I Transcription | 56 | 8.49e-01 | -0.014700 | 9.07e-01 |
| Synthesis of IP3 and IP4 in the cytosol | 22 | 9.06e-01 | 0.014600 | 9.49e-01 |
| RHO GTPases Activate NADPH Oxidases | 21 | 9.08e-01 | -0.014500 | 9.49e-01 |
| tRNA processing | 109 | 7.93e-01 | 0.014500 | 8.80e-01 |
| MTOR signalling | 40 | 8.75e-01 | -0.014400 | 9.26e-01 |
| SUMOylation | 168 | 7.50e-01 | 0.014300 | 8.52e-01 |
| tRNA modification in the nucleus and cytosol | 43 | 8.72e-01 | -0.014200 | 9.25e-01 |
| Cytosolic iron-sulfur cluster assembly | 13 | 9.30e-01 | -0.014100 | 9.63e-01 |
| RHOF GTPase cycle | 39 | 8.83e-01 | 0.013700 | 9.32e-01 |
| RAB GEFs exchange GTP for GDP on RABs | 87 | 8.27e-01 | -0.013600 | 8.95e-01 |
| Signaling by VEGF | 105 | 8.14e-01 | -0.013300 | 8.90e-01 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 20 | 9.20e-01 | 0.013000 | 9.56e-01 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 24 | 9.15e-01 | -0.012600 | 9.54e-01 |
| Signaling by BRAF and RAF1 fusions | 58 | 8.72e-01 | 0.012200 | 9.25e-01 |
| Signaling by FGFR1 in disease | 32 | 9.06e-01 | 0.012100 | 9.49e-01 |
| RAC3 GTPase cycle | 87 | 8.48e-01 | -0.011900 | 9.07e-01 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 17 | 9.34e-01 | 0.011600 | 9.64e-01 |
| G alpha (q) signalling events | 130 | 8.22e-01 | 0.011500 | 8.93e-01 |
| VEGFA-VEGFR2 Pathway | 96 | 8.52e-01 | -0.011100 | 9.10e-01 |
| Rab regulation of trafficking | 119 | 8.38e-01 | -0.010900 | 9.02e-01 |
| Generic Transcription Pathway | 1080 | 5.54e-01 | 0.010800 | 7.29e-01 |
| Signaling by Activin | 13 | 9.52e-01 | -0.009610 | 9.71e-01 |
| Signaling by ERBB2 TMD/JMD mutants | 20 | 9.42e-01 | -0.009460 | 9.68e-01 |
| HS-GAG degradation | 22 | 9.39e-01 | 0.009440 | 9.68e-01 |
| SUMOylation of RNA binding proteins | 47 | 9.11e-01 | 0.009430 | 9.51e-01 |
| Regulation of CDH11 Expression and Function | 27 | 9.33e-01 | -0.009380 | 9.64e-01 |
| Processing of Capped Intronless Pre-mRNA | 29 | 9.31e-01 | 0.009260 | 9.64e-01 |
| Signaling by ERBB4 | 51 | 9.10e-01 | -0.009120 | 9.51e-01 |
| Regulation of signaling by CBL | 22 | 9.42e-01 | -0.008940 | 9.68e-01 |
| Recognition of DNA damage by PCNA-containing replication complex | 30 | 9.34e-01 | 0.008700 | 9.64e-01 |
| RNA Polymerase II Transcription | 1198 | 6.20e-01 | 0.008590 | 7.74e-01 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 20 | 9.47e-01 | -0.008590 | 9.70e-01 |
| RNA Polymerase I Transcription Initiation | 47 | 9.20e-01 | -0.008510 | 9.56e-01 |
| Fatty acid metabolism | 140 | 8.63e-01 | 0.008430 | 9.19e-01 |
| Plasma lipoprotein clearance | 32 | 9.37e-01 | -0.008090 | 9.66e-01 |
| Synthesis of bile acids and bile salts via 27-hydroxycholesterol | 10 | 9.65e-01 | 0.007920 | 9.78e-01 |
| SARS-CoV-2 modulates autophagy | 11 | 9.64e-01 | 0.007840 | 9.78e-01 |
| Centrosome maturation | 79 | 9.06e-01 | -0.007660 | 9.49e-01 |
| Recruitment of mitotic centrosome proteins and complexes | 79 | 9.06e-01 | -0.007660 | 9.49e-01 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 63 | 9.17e-01 | -0.007640 | 9.54e-01 |
| Activated NOTCH1 Transmits Signal to the Nucleus | 30 | 9.43e-01 | 0.007520 | 9.68e-01 |
| RNA Polymerase I Transcription Termination | 30 | 9.44e-01 | 0.007400 | 9.68e-01 |
| Signaling by Retinoic Acid | 36 | 9.39e-01 | 0.007340 | 9.68e-01 |
| Amine ligand-binding receptors | 11 | 9.67e-01 | -0.007170 | 9.78e-01 |
| Processing of Capped Intron-Containing Pre-mRNA | 278 | 8.45e-01 | 0.006850 | 9.06e-01 |
| RHOA GTPase cycle | 143 | 8.88e-01 | 0.006820 | 9.35e-01 |
| Loss of Nlp from mitotic centrosomes | 67 | 9.24e-01 | 0.006720 | 9.59e-01 |
| Loss of proteins required for interphase microtubule organization from the centrosome | 67 | 9.24e-01 | 0.006720 | 9.59e-01 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants | 15 | 9.65e-01 | -0.006520 | 9.78e-01 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer | 15 | 9.65e-01 | -0.006520 | 9.78e-01 |
| WNT ligand biogenesis and trafficking | 17 | 9.64e-01 | 0.006390 | 9.78e-01 |
| Signaling by RAF1 mutants | 36 | 9.49e-01 | -0.006110 | 9.71e-01 |
| O-glycosylation of TSR domain-containing proteins | 35 | 9.52e-01 | 0.005840 | 9.71e-01 |
| Dual Incision in GG-NER | 41 | 9.50e-01 | 0.005710 | 9.71e-01 |
| Signaling by SCF-KIT | 41 | 9.51e-01 | 0.005600 | 9.71e-01 |
| Signaling by Hippo | 20 | 9.66e-01 | -0.005580 | 9.78e-01 |
| Telomere C-strand synthesis initiation | 13 | 9.73e-01 | -0.005510 | 9.81e-01 |
| GABA receptor activation | 40 | 9.54e-01 | 0.005310 | 9.71e-01 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 43 | 9.54e-01 | -0.005060 | 9.71e-01 |
| NoRC negatively regulates rRNA expression | 52 | 9.50e-01 | -0.005020 | 9.71e-01 |
| Cell death signalling via NRAGE, NRIF and NADE | 73 | 9.41e-01 | -0.004990 | 9.68e-01 |
| Negative epigenetic regulation of rRNA expression | 55 | 9.52e-01 | 0.004670 | 9.71e-01 |
| Transcriptional Regulation by NPAS4 | 30 | 9.65e-01 | 0.004660 | 9.78e-01 |
| HATs acetylate histones | 82 | 9.43e-01 | -0.004550 | 9.68e-01 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 16 | 9.76e-01 | -0.004390 | 9.82e-01 |
| SUMOylation of DNA replication proteins | 46 | 9.60e-01 | -0.004300 | 9.76e-01 |
| Nicotinate metabolism | 27 | 9.75e-01 | -0.003510 | 9.82e-01 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 40 | 9.72e-01 | 0.003260 | 9.80e-01 |
| Signaling by RAS mutants | 40 | 9.72e-01 | 0.003260 | 9.80e-01 |
| Signaling by moderate kinase activity BRAF mutants | 40 | 9.72e-01 | 0.003260 | 9.80e-01 |
| Signaling downstream of RAS mutants | 40 | 9.72e-01 | 0.003260 | 9.80e-01 |
| Cardiogenesis | 19 | 9.81e-01 | 0.003090 | 9.87e-01 |
| Nicotinamide salvaging | 16 | 9.83e-01 | 0.003000 | 9.88e-01 |
| Phase 2 - plateau phase | 10 | 9.90e-01 | -0.002240 | 9.93e-01 |
| Metabolism of lipids | 599 | 9.42e-01 | 0.001760 | 9.68e-01 |
| Interferon gamma signaling | 74 | 9.80e-01 | 0.001700 | 9.86e-01 |
| KSRP (KHSRP) binds and destabilizes mRNA | 17 | 9.91e-01 | 0.001610 | 9.93e-01 |
| Termination of translesion DNA synthesis | 31 | 9.90e-01 | 0.001260 | 9.93e-01 |
| Aquaporin-mediated transport | 36 | 9.90e-01 | -0.001220 | 9.93e-01 |
| Glucagon-type ligand receptors | 17 | 9.94e-01 | -0.001030 | 9.95e-01 |
| Thrombin signalling through proteinase activated receptors (PARs) | 24 | 9.94e-01 | 0.000941 | 9.95e-01 |
| AURKA Activation by TPX2 | 70 | 9.96e-01 | 0.000335 | 9.96e-01 |
Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane
| 698 | |
|---|---|
| set | Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane |
| setSize | 13 |
| pANOVA | 1.56e-05 |
| s.dist | -0.692 |
| p.adjustANOVA | 0.00011 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| TUBA4A | -8303 |
| GJA1 | -7862 |
| TUBA8 | -7620 |
| TUBB2A | -7115 |
| TUBB2B | -6815 |
| TUBB3 | -6598 |
| TUBB4B | -5898 |
| TUBA1C | -5471 |
| TUBB6 | -4118 |
| TUBA1B | -3972 |
| TUBA1A | -2543 |
| TUBAL3 | -1466 |
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| TUBA4A | -8303 |
| GJA1 | -7862 |
| TUBA8 | -7620 |
| TUBB2A | -7115 |
| TUBB2B | -6815 |
| TUBB3 | -6598 |
| TUBB4B | -5898 |
| TUBA1C | -5471 |
| TUBB6 | -4118 |
| TUBA1B | -3972 |
| TUBA1A | -2543 |
| TUBAL3 | -1466 |
Formation of tubulin folding intermediates by CCT/TriC
| 425 | |
|---|---|
| set | Formation of tubulin folding intermediates by CCT/TriC |
| setSize | 21 |
| pANOVA | 1.95e-07 |
| s.dist | -0.656 |
| p.adjustANOVA | 2.09e-06 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| TUBA4A | -8303 |
| CCT3 | -7729 |
| TUBA8 | -7620 |
| TUBB2A | -7115 |
| CCT7 | -7087 |
| TUBB2B | -6815 |
| CCT4 | -6628 |
| TUBB3 | -6598 |
| TCP1 | -6549 |
| TUBB4B | -5898 |
| CCT2 | -5655 |
| TUBA1C | -5471 |
| CCT8 | -4656 |
| TUBB6 | -4118 |
| CCT6A | -4055 |
| TUBA1B | -3972 |
| CCT5 | -3161 |
| CCT6B | -2853 |
| TUBA1A | -2543 |
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| TUBA4A | -8303 |
| CCT3 | -7729 |
| TUBA8 | -7620 |
| TUBB2A | -7115 |
| CCT7 | -7087 |
| TUBB2B | -6815 |
| CCT4 | -6628 |
| TUBB3 | -6598 |
| TCP1 | -6549 |
| TUBB4B | -5898 |
| CCT2 | -5655 |
| TUBA1C | -5471 |
| CCT8 | -4656 |
| TUBB6 | -4118 |
| CCT6A | -4055 |
| TUBA1B | -3972 |
| CCT5 | -3161 |
| CCT6B | -2853 |
| TUBA1A | -2543 |
| TUBAL3 | -1466 |
Transport of connexons to the plasma membrane
| 1394 | |
|---|---|
| set | Transport of connexons to the plasma membrane |
| setSize | 14 |
| pANOVA | 4.42e-05 |
| s.dist | -0.63 |
| p.adjustANOVA | 0.000294 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| TUBA4A | -8303 |
| GJA1 | -7862 |
| TUBA8 | -7620 |
| TUBB2A | -7115 |
| TUBB2B | -6815 |
| TUBB3 | -6598 |
| TUBB4B | -5898 |
| TUBA1C | -5471 |
| TUBB6 | -4118 |
| TUBA1B | -3972 |
| TUBA1A | -2543 |
| TUBAL3 | -1466 |
| GJB2 | 1325 |
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| TUBA4A | -8303 |
| GJA1 | -7862 |
| TUBA8 | -7620 |
| TUBB2A | -7115 |
| TUBB2B | -6815 |
| TUBB3 | -6598 |
| TUBB4B | -5898 |
| TUBA1C | -5471 |
| TUBB6 | -4118 |
| TUBA1B | -3972 |
| TUBA1A | -2543 |
| TUBAL3 | -1466 |
| GJB2 | 1325 |
Folding of actin by CCT/TriC
| 405 | |
|---|---|
| set | Folding of actin by CCT/TriC |
| setSize | 10 |
| pANOVA | 0.000871 |
| s.dist | -0.608 |
| p.adjustANOVA | 0.00437 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CCT3 | -7729 |
| CCT7 | -7087 |
| CCT4 | -6628 |
| TCP1 | -6549 |
| CCT2 | -5655 |
| CCT8 | -4656 |
| CCT6A | -4055 |
| ACTB | -3223 |
| CCT5 | -3161 |
| CCT6B | -2853 |
| GeneID | Gene Rank |
|---|---|
| CCT3 | -7729 |
| CCT7 | -7087 |
| CCT4 | -6628 |
| TCP1 | -6549 |
| CCT2 | -5655 |
| CCT8 | -4656 |
| CCT6A | -4055 |
| ACTB | -3223 |
| CCT5 | -3161 |
| CCT6B | -2853 |
Prefoldin mediated transfer of substrate to CCT/TriC
| 898 | |
|---|---|
| set | Prefoldin mediated transfer of substrate to CCT/TriC |
| setSize | 25 |
| pANOVA | 2.32e-07 |
| s.dist | -0.597 |
| p.adjustANOVA | 2.4e-06 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| TUBA4A | -8303 |
| PFDN2 | -8138 |
| CCT3 | -7729 |
| TUBB2A | -7115 |
| CCT7 | -7087 |
| TUBB2B | -6815 |
| CCT4 | -6628 |
| TUBB3 | -6598 |
| TCP1 | -6549 |
| PFDN1 | -6477 |
| TUBB4B | -5898 |
| CCT2 | -5655 |
| TUBA1C | -5471 |
| CCT8 | -4656 |
| PFDN5 | -4632 |
| TUBB6 | -4118 |
| CCT6A | -4055 |
| PFDN6 | -4013 |
| ACTB | -3223 |
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| TUBA4A | -8303 |
| PFDN2 | -8138 |
| CCT3 | -7729 |
| TUBB2A | -7115 |
| CCT7 | -7087 |
| TUBB2B | -6815 |
| CCT4 | -6628 |
| TUBB3 | -6598 |
| TCP1 | -6549 |
| PFDN1 | -6477 |
| TUBB4B | -5898 |
| CCT2 | -5655 |
| TUBA1C | -5471 |
| CCT8 | -4656 |
| PFDN5 | -4632 |
| TUBB6 | -4118 |
| CCT6A | -4055 |
| PFDN6 | -4013 |
| ACTB | -3223 |
| CCT5 | -3161 |
| CCT6B | -2853 |
| TUBA1A | -2543 |
| VBP1 | 75 |
| PFDN4 | 3324 |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding
| 225 | |
|---|---|
| set | Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding |
| setSize | 28 |
| pANOVA | 7.05e-08 |
| s.dist | -0.588 |
| p.adjustANOVA | 8.37e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| TUBA4A | -8303 |
| PFDN2 | -8138 |
| CCT3 | -7729 |
| TUBA8 | -7620 |
| TUBB2A | -7115 |
| CCT7 | -7087 |
| TUBB2B | -6815 |
| CCT4 | -6628 |
| TUBB3 | -6598 |
| TCP1 | -6549 |
| PFDN1 | -6477 |
| TUBB4B | -5898 |
| CCT2 | -5655 |
| TUBA1C | -5471 |
| CCT8 | -4656 |
| PFDN5 | -4632 |
| TUBB6 | -4118 |
| CCT6A | -4055 |
| PFDN6 | -4013 |
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| TUBA4A | -8303 |
| PFDN2 | -8138 |
| CCT3 | -7729 |
| TUBA8 | -7620 |
| TUBB2A | -7115 |
| CCT7 | -7087 |
| TUBB2B | -6815 |
| CCT4 | -6628 |
| TUBB3 | -6598 |
| TCP1 | -6549 |
| PFDN1 | -6477 |
| TUBB4B | -5898 |
| CCT2 | -5655 |
| TUBA1C | -5471 |
| CCT8 | -4656 |
| PFDN5 | -4632 |
| TUBB6 | -4118 |
| CCT6A | -4055 |
| PFDN6 | -4013 |
| TUBA1B | -3972 |
| ACTB | -3223 |
| CCT5 | -3161 |
| CCT6B | -2853 |
| TUBA1A | -2543 |
| TUBAL3 | -1466 |
| VBP1 | 75 |
| PFDN4 | 3324 |
Eukaryotic Translation Elongation
| 370 | |
|---|---|
| set | Eukaryotic Translation Elongation |
| setSize | 92 |
| pANOVA | 6.24e-22 |
| s.dist | -0.58 |
| p.adjustANOVA | 1.15e-19 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| EEF1A2 | -8395 |
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EEF2 | -7489 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| EEF1G | -6441 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| GeneID | Gene Rank |
|---|---|
| EEF1A2 | -8395 |
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EEF2 | -7489 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| EEF1G | -6441 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| EEF1B2 | -5421 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| EEF1D | -4712 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| EEF1A1P5 | -4398 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| EEF1A1 | -3602 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| RPS14 | -1548 |
| RPL36A | -1431 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
Josephin domain DUBs
| 616 | |
|---|---|
| set | Josephin domain DUBs |
| setSize | 10 |
| pANOVA | 0.00169 |
| s.dist | -0.573 |
| p.adjustANOVA | 0.00789 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| VCP | -7846 |
| UBB | -7624 |
| UBC | -7582 |
| JOSD1 | -6977 |
| RAD23A | -6962 |
| UBA52 | -6597 |
| RAD23B | -5777 |
| JOSD2 | -4891 |
| RPS27A | -2686 |
| ATXN3 | 8226 |
| GeneID | Gene Rank |
|---|---|
| VCP | -7846 |
| UBB | -7624 |
| UBC | -7582 |
| JOSD1 | -6977 |
| RAD23A | -6962 |
| UBA52 | -6597 |
| RAD23B | -5777 |
| JOSD2 | -4891 |
| RPS27A | -2686 |
| ATXN3 | 8226 |
Peptide chain elongation
| 856 | |
|---|---|
| set | Peptide chain elongation |
| setSize | 87 |
| pANOVA | 2.25e-20 |
| s.dist | -0.573 |
| p.adjustANOVA | 1.84e-18 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EEF2 | -7489 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EEF2 | -7489 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| EEF1A1 | -3602 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| RPS14 | -1548 |
| RPL36A | -1431 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
TP53 Regulates Transcription of Death Receptors and Ligands
| 1309 | |
|---|---|
| set | TP53 Regulates Transcription of Death Receptors and Ligands |
| setSize | 10 |
| pANOVA | 0.00184 |
| s.dist | -0.569 |
| p.adjustANOVA | 0.00853 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TNFRSF10C | -8405 |
| TNFRSF10D | -8116 |
| TP53BP2 | -6984 |
| IGFBP3 | -6885 |
| TNFRSF10B | -6801 |
| TP53 | -6483 |
| FAS | -3540 |
| TNFRSF10A | -2175 |
| TMEM219 | -1235 |
| PPP1R13B | 2282 |
| GeneID | Gene Rank |
|---|---|
| TNFRSF10C | -8405 |
| TNFRSF10D | -8116 |
| TP53BP2 | -6984 |
| IGFBP3 | -6885 |
| TNFRSF10B | -6801 |
| TP53 | -6483 |
| FAS | -3540 |
| TNFRSF10A | -2175 |
| TMEM219 | -1235 |
| PPP1R13B | 2282 |
Gluconeogenesis
| 482 | |
|---|---|
| set | Gluconeogenesis |
| setSize | 27 |
| pANOVA | 3.56e-07 |
| s.dist | -0.566 |
| p.adjustANOVA | 3.44e-06 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ALDOC | -8213 |
| PGAM1 | -8175 |
| TPI1 | -8029 |
| GPI | -7983 |
| ALDOA | -7961 |
| PGK1 | -7888 |
| PCK1 | -7730 |
| ENO1 | -7573 |
| SLC25A11 | -7530 |
| PC | -7155 |
| MDH2 | -7105 |
| SLC25A1 | -7036 |
| GAPDH | -6785 |
| SLC25A10 | -6556 |
| GOT1 | -6546 |
| ENO2 | -6414 |
| GOT2 | -5883 |
| MDH1 | -5842 |
| ENO3 | -4756 |
| G6PC3 | -3488 |
| GeneID | Gene Rank |
|---|---|
| ALDOC | -8213 |
| PGAM1 | -8175 |
| TPI1 | -8029 |
| GPI | -7983 |
| ALDOA | -7961 |
| PGK1 | -7888 |
| PCK1 | -7730 |
| ENO1 | -7573 |
| SLC25A11 | -7530 |
| PC | -7155 |
| MDH2 | -7105 |
| SLC25A1 | -7036 |
| GAPDH | -6785 |
| SLC25A10 | -6556 |
| GOT1 | -6546 |
| ENO2 | -6414 |
| GOT2 | -5883 |
| MDH1 | -5842 |
| ENO3 | -4756 |
| G6PC3 | -3488 |
| SLC25A12 | -2159 |
| FBP1 | 155 |
| SLC25A13 | 954 |
| SLC37A2 | 1836 |
| PCK2 | 1967 |
| SLC37A1 | 3055 |
| SLC37A4 | 3101 |
Viral mRNA Translation
| 1424 | |
|---|---|
| set | Viral mRNA Translation |
| setSize | 87 |
| pANOVA | 7.33e-20 |
| s.dist | -0.565 |
| p.adjustANOVA | 5e-18 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| DNAJC3 | -3136 |
| RPS7 | -3126 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| GRSF1 | -2289 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| RPS14 | -1548 |
| RPL36A | -1431 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
Erythrocytes take up carbon dioxide and release oxygen
| 364 | |
|---|---|
| set | Erythrocytes take up carbon dioxide and release oxygen |
| setSize | 10 |
| pANOVA | 0.00201 |
| s.dist | -0.564 |
| p.adjustANOVA | 0.00913 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HBB | -8432 |
| HBA1 | -8431 |
| SLC4A1 | -8426 |
| CA1 | -8338 |
| CA2 | -8322 |
| CYB5R1 | -7941 |
| CYB5R2 | -6458 |
| AQP1 | -2308 |
| CYB5R4 | 5115 |
| CYB5RL | 5605 |
| GeneID | Gene Rank |
|---|---|
| HBB | -8432 |
| HBA1 | -8431 |
| SLC4A1 | -8426 |
| CA1 | -8338 |
| CA2 | -8322 |
| CYB5R1 | -7941 |
| CYB5R2 | -6458 |
| AQP1 | -2308 |
| CYB5R4 | 5115 |
| CYB5RL | 5605 |
O2/CO2 exchange in erythrocytes
| 809 | |
|---|---|
| set | O2/CO2 exchange in erythrocytes |
| setSize | 10 |
| pANOVA | 0.00201 |
| s.dist | -0.564 |
| p.adjustANOVA | 0.00913 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HBB | -8432 |
| HBA1 | -8431 |
| SLC4A1 | -8426 |
| CA1 | -8338 |
| CA2 | -8322 |
| CYB5R1 | -7941 |
| CYB5R2 | -6458 |
| AQP1 | -2308 |
| CYB5R4 | 5115 |
| CYB5RL | 5605 |
| GeneID | Gene Rank |
|---|---|
| HBB | -8432 |
| HBA1 | -8431 |
| SLC4A1 | -8426 |
| CA1 | -8338 |
| CA2 | -8322 |
| CYB5R1 | -7941 |
| CYB5R2 | -6458 |
| AQP1 | -2308 |
| CYB5R4 | 5115 |
| CYB5RL | 5605 |
Keratan sulfate biosynthesis
| 619 | |
|---|---|
| set | Keratan sulfate biosynthesis |
| setSize | 26 |
| pANOVA | 6.42e-07 |
| s.dist | -0.564 |
| p.adjustANOVA | 6.02e-06 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ACAN | -8364 |
| ST3GAL2 | -7975 |
| CHST6 | -7948 |
| OMD | -7768 |
| B4GALT3 | -7638 |
| OGN | -7543 |
| B4GALT5 | -7319 |
| ST3GAL3 | -7316 |
| CHST1 | -7309 |
| LUM | -7308 |
| ST3GAL1 | -7307 |
| FMOD | -7200 |
| B4GALT1 | -7195 |
| B4GALT2 | -6989 |
| PRELP | -6737 |
| B4GALT4 | -6720 |
| ST3GAL4 | -6387 |
| B4GALT6 | -5564 |
| CHST5 | -4724 |
| B3GNT7 | -3337 |
| GeneID | Gene Rank |
|---|---|
| ACAN | -8364 |
| ST3GAL2 | -7975 |
| CHST6 | -7948 |
| OMD | -7768 |
| B4GALT3 | -7638 |
| OGN | -7543 |
| B4GALT5 | -7319 |
| ST3GAL3 | -7316 |
| CHST1 | -7309 |
| LUM | -7308 |
| ST3GAL1 | -7307 |
| FMOD | -7200 |
| B4GALT1 | -7195 |
| B4GALT2 | -6989 |
| PRELP | -6737 |
| B4GALT4 | -6720 |
| ST3GAL4 | -6387 |
| B4GALT6 | -5564 |
| CHST5 | -4724 |
| B3GNT7 | -3337 |
| KERA | -2985 |
| B4GAT1 | -1389 |
| SLC35D2 | 1766 |
| CHST2 | 3767 |
| ST3GAL6 | 6384 |
| B3GNT2 | 6610 |
Eukaryotic Translation Termination
| 372 | |
|---|---|
| set | Eukaryotic Translation Termination |
| setSize | 91 |
| pANOVA | 7.47e-20 |
| s.dist | -0.553 |
| p.adjustANOVA | 5e-18 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| GSPT1 | -7498 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| GSPT1 | -7498 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| APEH | -4731 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| TRMT112 | -3997 |
| RPL36AL | -3945 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| ETF1 | -2714 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| RPS14 | -1548 |
| RPL36A | -1431 |
| RPS4Y1 | -434 |
| GSPT2 | -212 |
| RPS26 | 851 |
| N6AMT1 | 4223 |
STAT3 nuclear events downstream of ALK signaling
| 1126 | |
|---|---|
| set | STAT3 nuclear events downstream of ALK signaling |
| setSize | 10 |
| pANOVA | 0.00281 |
| s.dist | -0.546 |
| p.adjustANOVA | 0.0122 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HIF1A | -8219 |
| IL2RG | -8157 |
| STAT3 | -7798 |
| PRDM1 | -7683 |
| HDAC1 | -5692 |
| CD274 | -4927 |
| SIN3A | -3893 |
| HDAC3 | -2263 |
| HDAC2 | -600 |
| EP300 | 2823 |
| GeneID | Gene Rank |
|---|---|
| HIF1A | -8219 |
| IL2RG | -8157 |
| STAT3 | -7798 |
| PRDM1 | -7683 |
| HDAC1 | -5692 |
| CD274 | -4927 |
| SIN3A | -3893 |
| HDAC3 | -2263 |
| HDAC2 | -600 |
| EP300 | 2823 |
SARS-CoV-1 modulates host translation machinery
| 1100 | |
|---|---|
| set | SARS-CoV-1 modulates host translation machinery |
| setSize | 36 |
| pANOVA | 1.45e-08 |
| s.dist | -0.546 |
| p.adjustANOVA | 2e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS19 | -7713 |
| RPS2 | -7641 |
| RPS29 | -7209 |
| RPS3 | -6819 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPSA | -6061 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPS15 | -5859 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPS16 | -5397 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPS6 | -5018 |
| RPS17 | -4895 |
| GeneID | Gene Rank |
|---|---|
| RPS19 | -7713 |
| RPS2 | -7641 |
| RPS29 | -7209 |
| RPS3 | -6819 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPSA | -6061 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPS15 | -5859 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPS16 | -5397 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPS6 | -5018 |
| RPS17 | -4895 |
| RPS25 | -4561 |
| RPS15A | -4397 |
| RPS10 | -4241 |
| RPS13 | -4077 |
| HNRNPA1 | -3944 |
| RPS27L | -3846 |
| EEF1A1 | -3602 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPS7 | -3126 |
| RPS27A | -2686 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| RPS14 | -1548 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
Formation of a pool of free 40S subunits
| 415 | |
|---|---|
| set | Formation of a pool of free 40S subunits |
| setSize | 99 |
| pANOVA | 1.09e-20 |
| s.dist | -0.542 |
| p.adjustANOVA | 1.12e-18 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EIF3I | -7463 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| EIF3B | -6355 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EIF3I | -7463 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| EIF3B | -6355 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| EIF3C | -5977 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| EIF3G | -5696 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| EIF3H | -4971 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| EIF3A | -4296 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| EIF3F | -4130 |
| EIF3K | -4108 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| EIF3L | -3920 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| EIF3D | -1816 |
| RPS14 | -1548 |
| EIF3J | -1514 |
| RPL36A | -1431 |
| EIF3E | -1084 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
| EIF3M | 1103 |
| EIF1AX | 6869 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
| 786 | |
|---|---|
| set | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
| setSize | 93 |
| pANOVA | 2.33e-19 |
| s.dist | -0.539 |
| p.adjustANOVA | 1.49e-17 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| GSPT1 | -7498 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| EIF4G1 | -6700 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| GSPT1 | -7498 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| EIF4G1 | -6700 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| RPS27L | -3846 |
| UPF1 | -3732 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| ETF1 | -2714 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| RPS14 | -1548 |
| RPL36A | -1431 |
| RPS4Y1 | -434 |
| GSPT2 | -212 |
| RPS26 | 851 |
| NCBP1 | 1670 |
| NCBP2 | 2498 |
| PABPC1 | 2772 |
Syndecan interactions
| 1266 | |
|---|---|
| set | Syndecan interactions |
| setSize | 26 |
| pANOVA | 2e-06 |
| s.dist | -0.539 |
| p.adjustANOVA | 1.61e-05 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ACTN1 | -8301 |
| SDC4 | -8048 |
| TNC | -7796 |
| ITGB5 | -7775 |
| TGFB1 | -7715 |
| COL1A1 | -7605 |
| PRKCA | -7526 |
| COL5A2 | -7285 |
| COL1A2 | -7023 |
| COL3A1 | -6980 |
| SDC1 | -6611 |
| CASK | -6607 |
| COL5A1 | -6582 |
| THBS1 | -6203 |
| ITGB1 | -5796 |
| TRAPPC4 | -5672 |
| FGF2 | -4492 |
| FN1 | -3998 |
| ITGA2 | -3587 |
| ITGB3 | -2858 |
| GeneID | Gene Rank |
|---|---|
| ACTN1 | -8301 |
| SDC4 | -8048 |
| TNC | -7796 |
| ITGB5 | -7775 |
| TGFB1 | -7715 |
| COL1A1 | -7605 |
| PRKCA | -7526 |
| COL5A2 | -7285 |
| COL1A2 | -7023 |
| COL3A1 | -6980 |
| SDC1 | -6611 |
| CASK | -6607 |
| COL5A1 | -6582 |
| THBS1 | -6203 |
| ITGB1 | -5796 |
| TRAPPC4 | -5672 |
| FGF2 | -4492 |
| FN1 | -3998 |
| ITGA2 | -3587 |
| ITGB3 | -2858 |
| ITGAV | -2688 |
| COL5A3 | -2134 |
| SDC3 | 35 |
| ITGB4 | 2824 |
| SDC2 | 4937 |
| ITGA6 | 6483 |
SRP-dependent cotranslational protein targeting to membrane
| 1125 | |
|---|---|
| set | SRP-dependent cotranslational protein targeting to membrane |
| setSize | 110 |
| pANOVA | 4e-22 |
| s.dist | -0.533 |
| p.adjustANOVA | 8.41e-20 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SSR4 | -8245 |
| SSR2 | -7984 |
| RPLP0 | -7891 |
| SRPRA | -7742 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| DDOST | -7516 |
| RPL28 | -7343 |
| RPN1 | -7287 |
| RPS29 | -7209 |
| SEC61A1 | -7144 |
| SRPRB | -7038 |
| SEC61B | -6986 |
| RPL36 | -6927 |
| SRP68 | -6916 |
| SRP54 | -6895 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| GeneID | Gene Rank |
|---|---|
| SSR4 | -8245 |
| SSR2 | -7984 |
| RPLP0 | -7891 |
| SRPRA | -7742 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| DDOST | -7516 |
| RPL28 | -7343 |
| RPN1 | -7287 |
| RPS29 | -7209 |
| SEC61A1 | -7144 |
| SRPRB | -7038 |
| SEC61B | -6986 |
| RPL36 | -6927 |
| SRP68 | -6916 |
| SRP54 | -6895 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| SSR1 | -6102 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPN2 | -5569 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| SSR3 | -5324 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| RPL22 | -2914 |
| SEC11A | -2831 |
| SEC61G | -2799 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| SPCS3 | -1847 |
| RPS14 | -1548 |
| RPL36A | -1431 |
| SRP72 | -905 |
| SRP14 | -847 |
| SPCS2 | -789 |
| RPS4Y1 | -434 |
| SEC11C | -280 |
| SRP19 | 755 |
| RPS26 | 851 |
| TRAM1 | 852 |
| SPCS1 | 3076 |
| SEC61A2 | 5235 |
| SRP9 | 5603 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10
| 737 | |
|---|---|
| set | NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 |
| setSize | 12 |
| pANOVA | 0.00147 |
| s.dist | 0.53 |
| p.adjustANOVA | 0.00691 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IKBKB | 8151 |
| TRIM25 | 8017 |
| CASP10 | 7076 |
| RNF135 | 7019 |
| IFIH1 | 6763 |
| CASP8 | 5048 |
| MAVS | 4991 |
| IKBKG | 3657 |
| CHUK | 3447 |
| TRIM4 | 2902 |
| RIPK1 | 766 |
| FADD | -5903 |
| GeneID | Gene Rank |
|---|---|
| IKBKB | 8151 |
| TRIM25 | 8017 |
| CASP10 | 7076 |
| RNF135 | 7019 |
| IFIH1 | 6763 |
| CASP8 | 5048 |
| MAVS | 4991 |
| IKBKG | 3657 |
| CHUK | 3447 |
| TRIM4 | 2902 |
| RIPK1 | 766 |
| FADD | -5903 |
Selenocysteine synthesis
| 1146 | |
|---|---|
| set | Selenocysteine synthesis |
| setSize | 91 |
| pANOVA | 2.7e-18 |
| s.dist | -0.529 |
| p.adjustANOVA | 1.47e-16 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| SARS1 | -6439 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| SARS1 | -6439 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| SEPHS2 | -2669 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| PSTK | -1922 |
| RPS14 | -1548 |
| RPL36A | -1431 |
| EEFSEC | -583 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
| SECISBP2 | 7132 |
| SEPSECS | 7682 |
Suppression of phagosomal maturation
| 1262 | |
|---|---|
| set | Suppression of phagosomal maturation |
| setSize | 13 |
| pANOVA | 0.000979 |
| s.dist | -0.528 |
| p.adjustANOVA | 0.00487 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NOS2 | -7912 |
| UBB | -7624 |
| UBC | -7582 |
| ATP6V1H | -7501 |
| UBA52 | -6597 |
| RAB5A | -5527 |
| KPNB1 | -5490 |
| CORO1A | -5479 |
| VPS33B | -4696 |
| RPS27A | -2686 |
| HGS | -1983 |
| RAB7A | -1650 |
| KPNA1 | 6323 |
| GeneID | Gene Rank |
|---|---|
| NOS2 | -7912 |
| UBB | -7624 |
| UBC | -7582 |
| ATP6V1H | -7501 |
| UBA52 | -6597 |
| RAB5A | -5527 |
| KPNB1 | -5490 |
| CORO1A | -5479 |
| VPS33B | -4696 |
| RPS27A | -2686 |
| HGS | -1983 |
| RAB7A | -1650 |
| KPNA1 | 6323 |
L13a-mediated translational silencing of Ceruloplasmin expression
| 625 | |
|---|---|
| set | L13a-mediated translational silencing of Ceruloplasmin expression |
| setSize | 109 |
| pANOVA | 1.67e-21 |
| s.dist | -0.528 |
| p.adjustANOVA | 2.05e-19 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EIF3I | -7463 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| EIF4G1 | -6700 |
| RPL39 | -6686 |
| EIF4A1 | -6650 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| EIF4H | -6563 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EIF3I | -7463 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| EIF4G1 | -6700 |
| RPL39 | -6686 |
| EIF4A1 | -6650 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| EIF4H | -6563 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| EIF3B | -6355 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| EIF3C | -5977 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| EIF3G | -5696 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| EIF2S1 | -5255 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| EIF3H | -4971 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| EIF3A | -4296 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| EIF3F | -4130 |
| EIF3K | -4108 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| EIF3L | -3920 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| EIF4B | -2967 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| EIF3D | -1816 |
| RPS14 | -1548 |
| EIF3J | -1514 |
| RPL36A | -1431 |
| EIF2S3 | -1428 |
| EIF3E | -1084 |
| EIF4E | -626 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
| EIF3M | 1103 |
| EIF4A2 | 1907 |
| PABPC1 | 2772 |
| EIF1AX | 6869 |
Chondroitin sulfate biosynthesis
| 187 | |
|---|---|
| set | Chondroitin sulfate biosynthesis |
| setSize | 16 |
| pANOVA | 0.000293 |
| s.dist | -0.523 |
| p.adjustANOVA | 0.00164 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CHSY1 | -8321 |
| BGN | -8013 |
| CHPF | -7970 |
| CHSY3 | -7843 |
| CHPF2 | -7355 |
| CHST3 | -6839 |
| CSGALNACT2 | -6646 |
| CSPG4 | -6110 |
| CHST11 | -6072 |
| CSGALNACT1 | -3878 |
| DCN | -2719 |
| CHST15 | -1427 |
| VCAN | -370 |
| CHST7 | 552 |
| CHST12 | 732 |
| CHST13 | 1089 |
| GeneID | Gene Rank |
|---|---|
| CHSY1 | -8321 |
| BGN | -8013 |
| CHPF | -7970 |
| CHSY3 | -7843 |
| CHPF2 | -7355 |
| CHST3 | -6839 |
| CSGALNACT2 | -6646 |
| CSPG4 | -6110 |
| CHST11 | -6072 |
| CSGALNACT1 | -3878 |
| DCN | -2719 |
| CHST15 | -1427 |
| VCAN | -370 |
| CHST7 | 552 |
| CHST12 | 732 |
| CHST13 | 1089 |
GTP hydrolysis and joining of the 60S ribosomal subunit
| 462 | |
|---|---|
| set | GTP hydrolysis and joining of the 60S ribosomal subunit |
| setSize | 110 |
| pANOVA | 4.06e-21 |
| s.dist | -0.52 |
| p.adjustANOVA | 4.6e-19 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EIF3I | -7463 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| EIF4G1 | -6700 |
| RPL39 | -6686 |
| EIF4A1 | -6650 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| EIF4H | -6563 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EIF3I | -7463 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| EIF4G1 | -6700 |
| RPL39 | -6686 |
| EIF4A1 | -6650 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| EIF4H | -6563 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| EIF3B | -6355 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| EIF3C | -5977 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| EIF3G | -5696 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| EIF2S1 | -5255 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| EIF3H | -4971 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| EIF3A | -4296 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| EIF3F | -4130 |
| EIF3K | -4108 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| EIF3L | -3920 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| EIF4B | -2967 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| EIF3D | -1816 |
| RPS14 | -1548 |
| EIF3J | -1514 |
| RPL36A | -1431 |
| EIF2S3 | -1428 |
| EIF3E | -1084 |
| EIF4E | -626 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
| EIF3M | 1103 |
| EIF5 | 1512 |
| EIF4A2 | 1907 |
| EIF5B | 3636 |
| EIF1AX | 6869 |
Activation of Matrix Metalloproteinases
| 41 | |
|---|---|
| set | Activation of Matrix Metalloproteinases |
| setSize | 23 |
| pANOVA | 1.61e-05 |
| s.dist | -0.52 |
| p.adjustANOVA | 0.000113 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MMP25 | -8415 |
| FURIN | -8373 |
| MMP13 | -8337 |
| MMP8 | -8334 |
| CTSK | -8215 |
| MMP11 | -8077 |
| MMP7 | -8023 |
| MMP14 | -7663 |
| ELANE | -7565 |
| TIMP1 | -7481 |
| MMP2 | -7197 |
| CTSG | -6676 |
| TPSAB1 | -5743 |
| MMP17 | -3627 |
| MMP9 | -3492 |
| TIMP2 | -2923 |
| COL18A1 | -2477 |
| MMP24 | -1649 |
| MMP16 | -138 |
| MMP3 | 140 |
| GeneID | Gene Rank |
|---|---|
| MMP25 | -8415 |
| FURIN | -8373 |
| MMP13 | -8337 |
| MMP8 | -8334 |
| CTSK | -8215 |
| MMP11 | -8077 |
| MMP7 | -8023 |
| MMP14 | -7663 |
| ELANE | -7565 |
| TIMP1 | -7481 |
| MMP2 | -7197 |
| CTSG | -6676 |
| TPSAB1 | -5743 |
| MMP17 | -3627 |
| MMP9 | -3492 |
| TIMP2 | -2923 |
| COL18A1 | -2477 |
| MMP24 | -1649 |
| MMP16 | -138 |
| MMP3 | 140 |
| MMP1 | 248 |
| MMP15 | 4756 |
| KLKB1 | 7615 |
Response of EIF2AK4 (GCN2) to amino acid deficiency
| 1086 | |
|---|---|
| set | Response of EIF2AK4 (GCN2) to amino acid deficiency |
| setSize | 99 |
| pANOVA | 6.14e-19 |
| s.dist | -0.517 |
| p.adjustANOVA | 3.48e-17 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ATF3 | -8371 |
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| ATF4 | -7427 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| GeneID | Gene Rank |
|---|---|
| ATF3 | -8371 |
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| ATF4 | -7427 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| CEBPB | -6235 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| TRIB3 | -5395 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| EIF2S1 | -5255 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| DDIT3 | -2931 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| RPS14 | -1548 |
| RPL36A | -1431 |
| EIF2S3 | -1428 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
| GCN1 | 902 |
| IMPACT | 2361 |
| CEBPG | 3606 |
| ATF2 | 4104 |
| ASNS | 4575 |
| EIF2AK4 | 5976 |
Keratan sulfate degradation
| 620 | |
|---|---|
| set | Keratan sulfate degradation |
| setSize | 13 |
| pANOVA | 0.00131 |
| s.dist | -0.515 |
| p.adjustANOVA | 0.00634 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ACAN | -8364 |
| OMD | -7768 |
| OGN | -7543 |
| LUM | -7308 |
| FMOD | -7200 |
| PRELP | -6737 |
| GNS | -3293 |
| KERA | -2985 |
| GLB1L | -2966 |
| HEXB | -2239 |
| GALNS | -1076 |
| HEXA | 215 |
| GLB1 | 274 |
| GeneID | Gene Rank |
|---|---|
| ACAN | -8364 |
| OMD | -7768 |
| OGN | -7543 |
| LUM | -7308 |
| FMOD | -7200 |
| PRELP | -6737 |
| GNS | -3293 |
| KERA | -2985 |
| GLB1L | -2966 |
| HEXB | -2239 |
| GALNS | -1076 |
| HEXA | 215 |
| GLB1 | 274 |
Crosslinking of collagen fibrils
| 230 | |
|---|---|
| set | Crosslinking of collagen fibrils |
| setSize | 14 |
| pANOVA | 0.000902 |
| s.dist | -0.512 |
| p.adjustANOVA | 0.0045 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| COL1A1 | -7605 |
| LOXL2 | -7226 |
| COL1A2 | -7023 |
| PXDN | -6680 |
| LOX | -6328 |
| PCOLCE | -5694 |
| LOXL4 | -5562 |
| LOXL3 | -4802 |
| TLL1 | -4604 |
| COL4A2 | -4395 |
| COL4A1 | -2499 |
| LOXL1 | -2004 |
| BMP1 | -1477 |
| COL4A5 | 4829 |
| GeneID | Gene Rank |
|---|---|
| COL1A1 | -7605 |
| LOXL2 | -7226 |
| COL1A2 | -7023 |
| PXDN | -6680 |
| LOX | -6328 |
| PCOLCE | -5694 |
| LOXL4 | -5562 |
| LOXL3 | -4802 |
| TLL1 | -4604 |
| COL4A2 | -4395 |
| COL4A1 | -2499 |
| LOXL1 | -2004 |
| BMP1 | -1477 |
| COL4A5 | 4829 |
Cap-dependent Translation Initiation
| 151 | |
|---|---|
| set | Cap-dependent Translation Initiation |
| setSize | 117 |
| pANOVA | 1.19e-21 |
| s.dist | -0.511 |
| p.adjustANOVA | 1.59e-19 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EIF4EBP1 | -7488 |
| EIF3I | -7463 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| EIF4G1 | -6700 |
| RPL39 | -6686 |
| EIF4A1 | -6650 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| EIF4H | -6563 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EIF4EBP1 | -7488 |
| EIF3I | -7463 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| EIF4G1 | -6700 |
| RPL39 | -6686 |
| EIF4A1 | -6650 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| EIF4H | -6563 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| EIF3B | -6355 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| EIF3C | -5977 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| EIF2B2 | -5837 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| EIF3G | -5696 |
| RPL23 | -5667 |
| EIF2B3 | -5631 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| EIF2S1 | -5255 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| EIF2B4 | -5119 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| EIF3H | -4971 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| EIF3A | -4296 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| EIF3F | -4130 |
| EIF3K | -4108 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| EIF3L | -3920 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| EIF4B | -2967 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| EIF3D | -1816 |
| EIF2B1 | -1712 |
| RPS14 | -1548 |
| EIF3J | -1514 |
| RPL36A | -1431 |
| EIF2S3 | -1428 |
| EIF3E | -1084 |
| EIF4E | -626 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
| EIF2B5 | 992 |
| EIF3M | 1103 |
| EIF5 | 1512 |
| EIF4A2 | 1907 |
| PABPC1 | 2772 |
| EIF5B | 3636 |
| EIF1AX | 6869 |
Eukaryotic Translation Initiation
| 371 | |
|---|---|
| set | Eukaryotic Translation Initiation |
| setSize | 117 |
| pANOVA | 1.19e-21 |
| s.dist | -0.511 |
| p.adjustANOVA | 1.59e-19 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EIF4EBP1 | -7488 |
| EIF3I | -7463 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| EIF4G1 | -6700 |
| RPL39 | -6686 |
| EIF4A1 | -6650 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| EIF4H | -6563 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| GeneID | Gene Rank |
|---|---|
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| EIF4EBP1 | -7488 |
| EIF3I | -7463 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| EIF4G1 | -6700 |
| RPL39 | -6686 |
| EIF4A1 | -6650 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| EIF4H | -6563 |
| RPL10 | -6551 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| EIF3B | -6355 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| EIF3C | -5977 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| EIF2B2 | -5837 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| EIF3G | -5696 |
| RPL23 | -5667 |
| EIF2B3 | -5631 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| RPL4 | -5262 |
| EIF2S1 | -5255 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| EIF2B4 | -5119 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| EIF3H | -4971 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| EIF3A | -4296 |
| RPS10 | -4241 |
| RPL6 | -4135 |
| EIF3F | -4130 |
| EIF3K | -4108 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| RPL36AL | -3945 |
| EIF3L | -3920 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| EIF4B | -2967 |
| RPL22 | -2914 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| EIF3D | -1816 |
| EIF2B1 | -1712 |
| RPS14 | -1548 |
| EIF3J | -1514 |
| RPL36A | -1431 |
| EIF2S3 | -1428 |
| EIF3E | -1084 |
| EIF4E | -626 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
| EIF2B5 | 992 |
| EIF3M | 1103 |
| EIF5 | 1512 |
| EIF4A2 | 1907 |
| PABPC1 | 2772 |
| EIF5B | 3636 |
| EIF1AX | 6869 |
ATF6 (ATF6-alpha) activates chaperones
| 21 | |
|---|---|
| set | ATF6 (ATF6-alpha) activates chaperones |
| setSize | 12 |
| pANOVA | 0.00223 |
| s.dist | -0.51 |
| p.adjustANOVA | 0.01 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CALR | -7915 |
| XBP1 | -7678 |
| ATF4 | -7427 |
| HSP90B1 | -6390 |
| MBTPS2 | -6278 |
| HSPA5 | -5540 |
| MBTPS1 | -5260 |
| NFYC | -3992 |
| ATF6 | -3883 |
| DDIT3 | -2931 |
| NFYA | 7 |
| NFYB | 5189 |
| GeneID | Gene Rank |
|---|---|
| CALR | -7915 |
| XBP1 | -7678 |
| ATF4 | -7427 |
| HSP90B1 | -6390 |
| MBTPS2 | -6278 |
| HSPA5 | -5540 |
| MBTPS1 | -5260 |
| NFYC | -3992 |
| ATF6 | -3883 |
| DDIT3 | -2931 |
| NFYA | 7 |
| NFYB | 5189 |
The role of GTSE1 in G2/M progression after G2 checkpoint
| 1336 | |
|---|---|
| set | The role of GTSE1 in G2/M progression after G2 checkpoint |
| setSize | 70 |
| pANOVA | 1.95e-13 |
| s.dist | -0.508 |
| p.adjustANOVA | 6.66e-12 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| CDKN1A | -8342 |
| TUBA4A | -8303 |
| PSMB5 | -7965 |
| PSMD8 | -7921 |
| UBB | -7624 |
| TUBA8 | -7620 |
| UBC | -7582 |
| PSMD3 | -7480 |
| PSMD9 | -7386 |
| PSMB7 | -7117 |
| TUBB2A | -7115 |
| PSMB4 | -7037 |
| PSMB6 | -6917 |
| PSMA5 | -6910 |
| PSMD13 | -6893 |
| TUBB2B | -6815 |
| TUBB3 | -6598 |
| UBA52 | -6597 |
| TP53 | -6483 |
| GeneID | Gene Rank |
|---|---|
| TUBB1 | -8378 |
| CDKN1A | -8342 |
| TUBA4A | -8303 |
| PSMB5 | -7965 |
| PSMD8 | -7921 |
| UBB | -7624 |
| TUBA8 | -7620 |
| UBC | -7582 |
| PSMD3 | -7480 |
| PSMD9 | -7386 |
| PSMB7 | -7117 |
| TUBB2A | -7115 |
| PSMB4 | -7037 |
| PSMB6 | -6917 |
| PSMA5 | -6910 |
| PSMD13 | -6893 |
| TUBB2B | -6815 |
| TUBB3 | -6598 |
| UBA52 | -6597 |
| TP53 | -6483 |
| PSMD4 | -6422 |
| PSMC4 | -6358 |
| PSMD14 | -6161 |
| TUBB4B | -5898 |
| PSMB3 | -5834 |
| PSMD2 | -5813 |
| PSME3 | -5779 |
| PSMC3 | -5689 |
| PSMF1 | -5641 |
| PSMD1 | -5563 |
| TUBA1C | -5471 |
| PSMA7 | -5396 |
| PSMD11 | -5049 |
| CCNB2 | -4988 |
| SEM1 | -4495 |
| PSMC5 | -4340 |
| HSP90AB1 | -4263 |
| PSME2 | -4227 |
| PSME1 | -4207 |
| TUBB6 | -4118 |
| PSMB9 | -4098 |
| TUBA1B | -3972 |
| PSMD7 | -3784 |
| PSMB2 | -3625 |
| PSMA4 | -3491 |
| PSMC1 | -3408 |
| MAPRE1 | -3322 |
| PSMA2 | -2957 |
| CCNB1 | -2814 |
| PLK1 | -2735 |
| RPS27A | -2686 |
| PSMA1 | -2611 |
| PSMD5 | -2546 |
| TUBA1A | -2543 |
| PSMD10 | -2427 |
| FKBPL | -2080 |
| PSME4 | -1789 |
| GTSE1 | -1661 |
| PSMD12 | -1659 |
| HSP90AA1 | -1568 |
| PSMB8 | -1549 |
| PSMB10 | -1521 |
| TUBAL3 | -1466 |
| PSMB1 | -1193 |
| PSMC2 | 264 |
| PSMA6 | 597 |
| PSMD6 | 664 |
| CDK1 | 1928 |
| PSMA3 | 2875 |
| PSMC6 | 6135 |
Formation of ATP by chemiosmotic coupling
| 406 | |
|---|---|
| set | Formation of ATP by chemiosmotic coupling |
| setSize | 16 |
| pANOVA | 0.000509 |
| s.dist | -0.502 |
| p.adjustANOVA | 0.00269 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ATP5F1B | -7774 |
| ATP5ME | -7752 |
| ATP5F1A | -6886 |
| ATP5MC3 | -6852 |
| ATP5F1E | -6399 |
| ATP5MC1 | -5875 |
| ATP5MC2 | -5470 |
| ATP5MG | -5171 |
| ATP5PF | -5034 |
| ATP5MF | -4836 |
| ATP5F1D | -4608 |
| ATP5PD | -2297 |
| ATP5PB | -1529 |
| ATP5F1C | -1025 |
| ATP5PO | -562 |
| DMAC2L | 3684 |
| GeneID | Gene Rank |
|---|---|
| ATP5F1B | -7774 |
| ATP5ME | -7752 |
| ATP5F1A | -6886 |
| ATP5MC3 | -6852 |
| ATP5F1E | -6399 |
| ATP5MC1 | -5875 |
| ATP5MC2 | -5470 |
| ATP5MG | -5171 |
| ATP5PF | -5034 |
| ATP5MF | -4836 |
| ATP5F1D | -4608 |
| ATP5PD | -2297 |
| ATP5PB | -1529 |
| ATP5F1C | -1025 |
| ATP5PO | -562 |
| DMAC2L | 3684 |
Ubiquitin-dependent degradation of Cyclin D
| 1409 | |
|---|---|
| set | Ubiquitin-dependent degradation of Cyclin D |
| setSize | 50 |
| pANOVA | 1.02e-09 |
| s.dist | -0.499 |
| p.adjustANOVA | 2.06e-08 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PSMB5 | -7965 |
| PSMD8 | -7921 |
| UBB | -7624 |
| UBC | -7582 |
| PSMD3 | -7480 |
| PSMD9 | -7386 |
| PSMB7 | -7117 |
| PSMB4 | -7037 |
| CDK4 | -7026 |
| PSMB6 | -6917 |
| PSMA5 | -6910 |
| PSMD13 | -6893 |
| UBA52 | -6597 |
| CCND1 | -6574 |
| PSMD4 | -6422 |
| PSMC4 | -6358 |
| PSMD14 | -6161 |
| PSMB3 | -5834 |
| PSMD2 | -5813 |
| PSME3 | -5779 |
| GeneID | Gene Rank |
|---|---|
| PSMB5 | -7965 |
| PSMD8 | -7921 |
| UBB | -7624 |
| UBC | -7582 |
| PSMD3 | -7480 |
| PSMD9 | -7386 |
| PSMB7 | -7117 |
| PSMB4 | -7037 |
| CDK4 | -7026 |
| PSMB6 | -6917 |
| PSMA5 | -6910 |
| PSMD13 | -6893 |
| UBA52 | -6597 |
| CCND1 | -6574 |
| PSMD4 | -6422 |
| PSMC4 | -6358 |
| PSMD14 | -6161 |
| PSMB3 | -5834 |
| PSMD2 | -5813 |
| PSME3 | -5779 |
| PSMC3 | -5689 |
| PSMF1 | -5641 |
| PSMD1 | -5563 |
| PSMA7 | -5396 |
| PSMD11 | -5049 |
| SEM1 | -4495 |
| PSMC5 | -4340 |
| PSME2 | -4227 |
| PSME1 | -4207 |
| PSMB9 | -4098 |
| PSMD7 | -3784 |
| PSMB2 | -3625 |
| PSMA4 | -3491 |
| PSMC1 | -3408 |
| PSMA2 | -2957 |
| RPS27A | -2686 |
| PSMA1 | -2611 |
| PSMD5 | -2546 |
| PSMD10 | -2427 |
| PSME4 | -1789 |
| PSMD12 | -1659 |
| PSMB8 | -1549 |
| PSMB10 | -1521 |
| GSK3B | -1282 |
| PSMB1 | -1193 |
| PSMC2 | 264 |
| PSMA6 | 597 |
| PSMD6 | 664 |
| PSMA3 | 2875 |
| PSMC6 | 6135 |
Formation of the ternary complex, and subsequently, the 43S complex
| 424 | |
|---|---|
| set | Formation of the ternary complex, and subsequently, the 43S complex |
| setSize | 51 |
| pANOVA | 7.02e-10 |
| s.dist | -0.499 |
| p.adjustANOVA | 1.5e-08 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS19 | -7713 |
| RPS2 | -7641 |
| EIF3I | -7463 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPS3 | -6819 |
| EIF3B | -6355 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPSA | -6061 |
| RPS28 | -6047 |
| EIF3C | -5977 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPS15 | -5859 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| EIF3G | -5696 |
| RPS16 | -5397 |
| GeneID | Gene Rank |
|---|---|
| RPS19 | -7713 |
| RPS2 | -7641 |
| EIF3I | -7463 |
| RPS29 | -7209 |
| EIF2S2 | -6998 |
| RPS3 | -6819 |
| EIF3B | -6355 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPSA | -6061 |
| RPS28 | -6047 |
| EIF3C | -5977 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPS15 | -5859 |
| RPS12 | -5766 |
| RPS21 | -5750 |
| EIF3G | -5696 |
| RPS16 | -5397 |
| EIF2S1 | -5255 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| RPS6 | -5018 |
| EIF3H | -4971 |
| RPS17 | -4895 |
| RPS25 | -4561 |
| RPS15A | -4397 |
| EIF3A | -4296 |
| RPS10 | -4241 |
| EIF3F | -4130 |
| EIF3K | -4108 |
| RPS13 | -4077 |
| EIF3L | -3920 |
| RPS27L | -3846 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPS7 | -3126 |
| RPS27A | -2686 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| EIF3D | -1816 |
| RPS14 | -1548 |
| EIF3J | -1514 |
| EIF2S3 | -1428 |
| EIF3E | -1084 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
| EIF3M | 1103 |
| EIF1AX | 6869 |
Selenoamino acid metabolism
| 1145 | |
|---|---|
| set | Selenoamino acid metabolism |
| setSize | 113 |
| pANOVA | 6.11e-20 |
| s.dist | -0.498 |
| p.adjustANOVA | 4.49e-18 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NNMT | -8359 |
| IARS1 | -8069 |
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| PAPSS1 | -6632 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| GSR | -6531 |
| PAPSS2 | -6522 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| GeneID | Gene Rank |
|---|---|
| NNMT | -8359 |
| IARS1 | -8069 |
| RPLP0 | -7891 |
| RPS19 | -7713 |
| RPL3 | -7686 |
| RPS2 | -7641 |
| RPL28 | -7343 |
| RPS29 | -7209 |
| RPL36 | -6927 |
| RPS3 | -6819 |
| RPL18 | -6766 |
| RPL39 | -6686 |
| PAPSS1 | -6632 |
| RPL27A | -6629 |
| UBA52 | -6597 |
| RPL10 | -6551 |
| GSR | -6531 |
| PAPSS2 | -6522 |
| RPL41 | -6496 |
| RPL19 | -6464 |
| SARS1 | -6439 |
| RPL37 | -6352 |
| RPL8 | -6270 |
| AHCY | -6266 |
| EPRS1 | -6259 |
| RPS18 | -6137 |
| RPS27 | -6115 |
| RPL10A | -6065 |
| RPSA | -6061 |
| RPL37A | -6055 |
| RPS28 | -6047 |
| FAU | -5935 |
| RPS8 | -5932 |
| RPS5 | -5915 |
| RPLP1 | -5910 |
| RPS15 | -5859 |
| RPL18A | -5814 |
| RPL17 | -5781 |
| RPS12 | -5766 |
| KARS1 | -5754 |
| RPS21 | -5750 |
| RPL13 | -5738 |
| RPL23 | -5667 |
| RPL12 | -5612 |
| RPL38 | -5491 |
| RPS16 | -5397 |
| RPL29 | -5304 |
| RPL26L1 | -5277 |
| MARS1 | -5275 |
| RPL4 | -5262 |
| RPL11 | -5228 |
| RPS4X | -5190 |
| RPS11 | -5164 |
| RPS9 | -5156 |
| CBS | -5110 |
| RPL39L | -5101 |
| RPS6 | -5018 |
| RPL5 | -5006 |
| RPS17 | -4895 |
| RPL13A | -4781 |
| RPLP2 | -4734 |
| RPL7A | -4579 |
| RPS25 | -4561 |
| RPL32 | -4542 |
| RPL35 | -4472 |
| RPS15A | -4397 |
| RPL27 | -4324 |
| RPS10 | -4241 |
| CTH | -4216 |
| RPL6 | -4135 |
| RPL15 | -4083 |
| RPS13 | -4077 |
| DARS1 | -4015 |
| RPL36AL | -3945 |
| RPS27L | -3846 |
| RPL34 | -3631 |
| RPL31 | -3604 |
| RPS23 | -3513 |
| RPS24 | -3505 |
| RPL30 | -3369 |
| RPL26 | -3362 |
| RPL35A | -3274 |
| RPL22L1 | -3218 |
| RPS7 | -3126 |
| TXNRD1 | -3009 |
| RPL22 | -2914 |
| RARS1 | -2859 |
| SCLY | -2832 |
| RPL14 | -2783 |
| RPL24 | -2780 |
| RPS27A | -2686 |
| SEPHS2 | -2669 |
| EEF1E1 | -2643 |
| RPL21 | -2556 |
| RPL23A | -2408 |
| RPL7 | -2349 |
| RPL9 | -2284 |
| RPS3A | -2257 |
| RPS20 | -2207 |
| PSTK | -1922 |
| RPS14 | -1548 |
| RPL36A | -1431 |
| AIMP2 | -1306 |
| QARS1 | -959 |
| EEFSEC | -583 |
| RPS4Y1 | -434 |
| RPS26 | 851 |
| INMT | 1205 |
| LARS1 | 4115 |
| AIMP1 | 4650 |
| SECISBP2 | 7132 |
| SEPSECS | 7682 |
| HNMT | 7964 |
Diseases associated with glycosaminoglycan metabolism
| 303 | |
|---|---|
| set | Diseases associated with glycosaminoglycan metabolism |
| setSize | 38 |
| pANOVA | 1.11e-07 |
| s.dist | -0.497 |
| p.adjustANOVA | 1.26e-06 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ACAN | -8364 |
| CHSY1 | -8321 |
| SDC4 | -8048 |
| BGN | -8013 |
| CHST6 | -7948 |
| OMD | -7768 |
| OGN | -7543 |
| ST3GAL3 | -7316 |
| LUM | -7308 |
| FMOD | -7200 |
| B4GALT1 | -7195 |
| CHST3 | -6839 |
| PRELP | -6737 |
| SDC1 | -6611 |
| PAPSS2 | -6522 |
| GPC1 | -6200 |
| B4GALT7 | -6121 |
| CSPG4 | -6110 |
| CHST14 | -6039 |
| GPC4 | -5879 |
| GeneID | Gene Rank |
|---|---|
| ACAN | -8364 |
| CHSY1 | -8321 |
| SDC4 | -8048 |
| BGN | -8013 |
| CHST6 | -7948 |
| OMD | -7768 |
| OGN | -7543 |
| ST3GAL3 | -7316 |
| LUM | -7308 |
| FMOD | -7200 |
| B4GALT1 | -7195 |
| CHST3 | -6839 |
| PRELP | -6737 |
| SDC1 | -6611 |
| PAPSS2 | -6522 |
| GPC1 | -6200 |
| B4GALT7 | -6121 |
| CSPG4 | -6110 |
| CHST14 | -6039 |
| GPC4 | -5879 |
| EXT2 | -5388 |
| B3GALT6 | -4999 |
| B3GAT3 | -4856 |
| GPC2 | -4119 |
| EXT1 | -3061 |
| KERA | -2985 |
| GPC3 | -2869 |
| DCN | -2719 |
| HEXB | -2239 |
| GPC6 | -2035 |
| VCAN | -370 |
| SDC3 | 35 |
| HEXA | 215 |
| SLC26A2 | 1922 |
| HSPG2 | 2113 |
| AGRN | 2896 |
| GPC5 | 4797 |
| SDC2 | 4937 |
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism
| 1061 | |
|---|---|
| set | Regulation of glycolysis by fructose 2,6-bisphosphate metabolism |
| setSize | 10 |
| pANOVA | 0.0066 |
| s.dist | -0.496 |
| p.adjustANOVA | 0.0255 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PFKFB3 | -7602 |
| PFKFB4 | -7348 |
| PRKACA | -6997 |
| PPP2CA | -6608 |
| PPP2R1A | -6444 |
| PPP2R1B | -5899 |
| PPP2CB | -3850 |
| PPP2R5D | -3521 |
| PFKFB2 | 1523 |
| PRKACB | 4470 |
| GeneID | Gene Rank |
|---|---|
| PFKFB3 | -7602 |
| PFKFB4 | -7348 |
| PRKACA | -6997 |
| PPP2CA | -6608 |
| PPP2R1A | -6444 |
| PPP2R1B | -5899 |
| PPP2CB | -3850 |
| PPP2R5D | -3521 |
| PFKFB2 | 1523 |
| PRKACB | 4470 |
FGFR2 ligand binding and activation
| 387 | |
|---|---|
| set | FGFR2 ligand binding and activation |
| setSize | 10 |
| pANOVA | 0.00697 |
| s.dist | -0.493 |
| p.adjustANOVA | 0.0267 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| FGF1 | -8390 |
| FGFR2 | -7930 |
| FGF9 | -7159 |
| FGF18 | -6599 |
| FGF23 | -6140 |
| FGF7 | -5852 |
| FGF2 | -4492 |
| FGFBP2 | -1081 |
| FGFBP3 | 782 |
| FGF10 | 4867 |
| GeneID | Gene Rank |
|---|---|
| FGF1 | -8390 |
| FGFR2 | -7930 |
| FGF9 | -7159 |
| FGF18 | -6599 |
| FGF23 | -6140 |
| FGF7 | -5852 |
| FGF2 | -4492 |
| FGFBP2 | -1081 |
| FGFBP3 | 782 |
| FGF10 | 4867 |
Downregulation of ERBB2:ERBB3 signaling
| 321 | |
|---|---|
| set | Downregulation of ERBB2:ERBB3 signaling |
| setSize | 13 |
| pANOVA | 0.00211 |
| s.dist | -0.492 |
| p.adjustANOVA | 0.00955 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| AKT1 | -7935 |
| RNF41 | -7916 |
| UBB | -7624 |
| UBC | -7582 |
| NRG2 | -7177 |
| UBA52 | -6597 |
| ERBB2 | -3246 |
| RPS27A | -2686 |
| NRG1 | -2384 |
| AKT2 | -2374 |
| AKT3 | -2058 |
| ERBB3 | -1444 |
| USP8 | 4473 |
| GeneID | Gene Rank |
|---|---|
| AKT1 | -7935 |
| RNF41 | -7916 |
| UBB | -7624 |
| UBC | -7582 |
| NRG2 | -7177 |
| UBA52 | -6597 |
| ERBB2 | -3246 |
| RPS27A | -2686 |
| NRG1 | -2384 |
| AKT2 | -2374 |
| AKT3 | -2058 |
| ERBB3 | -1444 |
| USP8 | 4473 |
Response of EIF2AK1 (HRI) to heme deficiency
| 1085 | |
|---|---|
| set | Response of EIF2AK1 (HRI) to heme deficiency |
| setSize | 14 |
| pANOVA | 0.00144 |
| s.dist | -0.492 |
| p.adjustANOVA | 0.00687 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ATF3 | -8371 |
| PPP1R15A | -8302 |
| EIF2AK1 | -7490 |
| ATF4 | -7427 |
| EIF2S2 | -6998 |
| ATF5 | -6882 |
| CEBPB | -6235 |
| TRIB3 | -5395 |
| EIF2S1 | -5255 |
| DDIT3 | -2931 |
| EIF2S3 | -1428 |
| GRB10 | -145 |
| CEBPG | 3606 |
| ASNS | 4575 |
| GeneID | Gene Rank |
|---|---|
| ATF3 | -8371 |
| PPP1R15A | -8302 |
| EIF2AK1 | -7490 |
| ATF4 | -7427 |
| EIF2S2 | -6998 |
| ATF5 | -6882 |
| CEBPB | -6235 |
| TRIB3 | -5395 |
| EIF2S1 | -5255 |
| DDIT3 | -2931 |
| EIF2S3 | -1428 |
| GRB10 | -145 |
| CEBPG | 3606 |
| ASNS | 4575 |
Membrane binding and targetting of GAG proteins
| 673 | |
|---|---|
| set | Membrane binding and targetting of GAG proteins |
| setSize | 14 |
| pANOVA | 0.00145 |
| s.dist | -0.491 |
| p.adjustANOVA | 0.00687 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| VPS37B | -7749 |
| UBB | -7624 |
| UBC | -7582 |
| UBA52 | -6597 |
| VPS37A | -6504 |
| VPS37D | -5978 |
| UBAP1 | -5775 |
| VPS37C | -4775 |
| TSG101 | -3035 |
| RPS27A | -2686 |
| MVB12A | -2524 |
| VPS28 | -1060 |
| MVB12B | -1050 |
| NMT2 | 4311 |
| GeneID | Gene Rank |
|---|---|
| VPS37B | -7749 |
| UBB | -7624 |
| UBC | -7582 |
| UBA52 | -6597 |
| VPS37A | -6504 |
| VPS37D | -5978 |
| UBAP1 | -5775 |
| VPS37C | -4775 |
| TSG101 | -3035 |
| RPS27A | -2686 |
| MVB12A | -2524 |
| VPS28 | -1060 |
| MVB12B | -1050 |
| NMT2 | 4311 |
Synthesis And Processing Of GAG, GAGPOL Polyproteins
| 1267 | |
|---|---|
| set | Synthesis And Processing Of GAG, GAGPOL Polyproteins |
| setSize | 14 |
| pANOVA | 0.00145 |
| s.dist | -0.491 |
| p.adjustANOVA | 0.00687 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| VPS37B | -7749 |
| UBB | -7624 |
| UBC | -7582 |
| UBA52 | -6597 |
| VPS37A | -6504 |
| VPS37D | -5978 |
| UBAP1 | -5775 |
| VPS37C | -4775 |
| TSG101 | -3035 |
| RPS27A | -2686 |
| MVB12A | -2524 |
| VPS28 | -1060 |
| MVB12B | -1050 |
| NMT2 | 4311 |
| GeneID | Gene Rank |
|---|---|
| VPS37B | -7749 |
| UBB | -7624 |
| UBC | -7582 |
| UBA52 | -6597 |
| VPS37A | -6504 |
| VPS37D | -5978 |
| UBAP1 | -5775 |
| VPS37C | -4775 |
| TSG101 | -3035 |
| RPS27A | -2686 |
| MVB12A | -2524 |
| VPS28 | -1060 |
| MVB12B | -1050 |
| NMT2 | 4311 |
Keratan sulfate/keratin metabolism
| 621 | |
|---|---|
| set | Keratan sulfate/keratin metabolism |
| setSize | 32 |
| pANOVA | 1.58e-06 |
| s.dist | -0.49 |
| p.adjustANOVA | 1.3e-05 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ACAN | -8364 |
| ST3GAL2 | -7975 |
| CHST6 | -7948 |
| OMD | -7768 |
| B4GALT3 | -7638 |
| OGN | -7543 |
| B4GALT5 | -7319 |
| ST3GAL3 | -7316 |
| CHST1 | -7309 |
| LUM | -7308 |
| ST3GAL1 | -7307 |
| FMOD | -7200 |
| B4GALT1 | -7195 |
| B4GALT2 | -6989 |
| PRELP | -6737 |
| B4GALT4 | -6720 |
| ST3GAL4 | -6387 |
| B4GALT6 | -5564 |
| CHST5 | -4724 |
| B3GNT7 | -3337 |
| GeneID | Gene Rank |
|---|---|
| ACAN | -8364 |
| ST3GAL2 | -7975 |
| CHST6 | -7948 |
| OMD | -7768 |
| B4GALT3 | -7638 |
| OGN | -7543 |
| B4GALT5 | -7319 |
| ST3GAL3 | -7316 |
| CHST1 | -7309 |
| LUM | -7308 |
| ST3GAL1 | -7307 |
| FMOD | -7200 |
| B4GALT1 | -7195 |
| B4GALT2 | -6989 |
| PRELP | -6737 |
| B4GALT4 | -6720 |
| ST3GAL4 | -6387 |
| B4GALT6 | -5564 |
| CHST5 | -4724 |
| B3GNT7 | -3337 |
| GNS | -3293 |
| KERA | -2985 |
| GLB1L | -2966 |
| HEXB | -2239 |
| B4GAT1 | -1389 |
| GALNS | -1076 |
| HEXA | 215 |
| GLB1 | 274 |
| SLC35D2 | 1766 |
| CHST2 | 3767 |
| ST3GAL6 | 6384 |
| B3GNT2 | 6610 |
Diseases associated with glycosylation precursor biosynthesis
| 304 | |
|---|---|
| set | Diseases associated with glycosylation precursor biosynthesis |
| setSize | 15 |
| pANOVA | 0.00102 |
| s.dist | -0.49 |
| p.adjustANOVA | 0.00503 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PGM1 | -8126 |
| GALE | -7608 |
| GFPT1 | -7478 |
| DPM2 | -7132 |
| GALK1 | -6827 |
| DHDDS | -6743 |
| PMM2 | -6182 |
| GNE | -5686 |
| DPM3 | -4884 |
| DOLK | -4512 |
| MPI | -3156 |
| NUS1 | -3073 |
| SRD5A3 | 1170 |
| DPM1 | 3703 |
| GALT | 3901 |
| GeneID | Gene Rank |
|---|---|
| PGM1 | -8126 |
| GALE | -7608 |
| GFPT1 | -7478 |
| DPM2 | -7132 |
| GALK1 | -6827 |
| DHDDS | -6743 |
| PMM2 | -6182 |
| GNE | -5686 |
| DPM3 | -4884 |
| DOLK | -4512 |
| MPI | -3156 |
| NUS1 | -3073 |
| SRD5A3 | 1170 |
| DPM1 | 3703 |
| GALT | 3901 |
Regulation of RUNX3 expression and activity
| 1044 | |
|---|---|
| set | Regulation of RUNX3 expression and activity |
| setSize | 55 |
| pANOVA | 4.18e-10 |
| s.dist | -0.487 |
| p.adjustANOVA | 9.45e-09 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PSMB5 | -7965 |
| PSMD8 | -7921 |
| TGFB1 | -7715 |
| UBB | -7624 |
| UBC | -7582 |
| PSMD3 | -7480 |
| SMURF1 | -7435 |
| SRC | -7389 |
| PSMD9 | -7386 |
| RUNX3 | -7378 |
| PSMB7 | -7117 |
| PSMB4 | -7037 |
| PSMB6 | -6917 |
| PSMA5 | -6910 |
| PSMD13 | -6893 |
| UBA52 | -6597 |
| PSMD4 | -6422 |
| PSMC4 | -6358 |
| PSMD14 | -6161 |
| PSMB3 | -5834 |
| GeneID | Gene Rank |
|---|---|
| PSMB5 | -7965 |
| PSMD8 | -7921 |
| TGFB1 | -7715 |
| UBB | -7624 |
| UBC | -7582 |
| PSMD3 | -7480 |
| SMURF1 | -7435 |
| SRC | -7389 |
| PSMD9 | -7386 |
| RUNX3 | -7378 |
| PSMB7 | -7117 |
| PSMB4 | -7037 |
| PSMB6 | -6917 |
| PSMA5 | -6910 |
| PSMD13 | -6893 |
| UBA52 | -6597 |
| PSMD4 | -6422 |
| PSMC4 | -6358 |
| PSMD14 | -6161 |
| PSMB3 | -5834 |
| PSMD2 | -5813 |
| PSME3 | -5779 |
| PSMC3 | -5689 |
| PSMF1 | -5641 |
| PSMD1 | -5563 |
| PSMA7 | -5396 |
| PSMD11 | -5049 |
| CDKN2A | -4644 |
| SEM1 | -4495 |
| MDM2 | -4394 |
| PSMC5 | -4340 |
| PSME2 | -4227 |
| PSME1 | -4207 |
| PSMB9 | -4098 |
| PSMD7 | -3784 |
| PSMB2 | -3625 |
| PSMA4 | -3491 |
| PSMC1 | -3408 |
| PSMA2 | -2957 |
| RPS27A | -2686 |
| PSMA1 | -2611 |
| PSMD5 | -2546 |
| PSMD10 | -2427 |
| CBFB | -1713 |
| PSMD12 | -1659 |
| PSMB8 | -1549 |
| PSMB10 | -1521 |
| PSMB1 | -1193 |
| PSMC2 | 264 |
| PSMA6 | 597 |
| PSMD6 | 664 |
| EP300 | 2823 |
| PSMA3 | 2875 |
| SMURF2 | 5575 |
| PSMC6 | 6135 |
Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.3.2 (2023-10-31)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 22.04.4 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.10.0
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.10.0
##
## locale:
## [1] LC_CTYPE=en_AU.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_AU.UTF-8 LC_COLLATE=en_AU.UTF-8
## [5] LC_MONETARY=en_AU.UTF-8 LC_MESSAGES=en_AU.UTF-8
## [7] LC_PAPER=en_AU.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_AU.UTF-8 LC_IDENTIFICATION=C
##
## time zone: Australia/Melbourne
## tzcode source: system (glibc)
##
## attached base packages:
## [1] stats4 stats graphics grDevices utils datasets methods
## [8] base
##
## other attached packages:
## [1] pkgload_1.3.3 GGally_2.2.0
## [3] beeswarm_0.4.0 gtools_3.9.5
## [5] echarts4r_0.4.5 kableExtra_1.3.4
## [7] topconfects_1.18.0 limma_3.58.1
## [9] eulerr_7.0.0 mitch_1.14.0
## [11] MASS_7.3-60 fgsea_1.28.0
## [13] gplots_3.1.3 DESeq2_1.42.0
## [15] SummarizedExperiment_1.32.0 Biobase_2.62.0
## [17] MatrixGenerics_1.14.0 matrixStats_1.2.0
## [19] GenomicRanges_1.54.1 GenomeInfoDb_1.38.5
## [21] IRanges_2.36.0 S4Vectors_0.40.2
## [23] BiocGenerics_0.48.1 reshape2_1.4.4
## [25] lubridate_1.9.3 forcats_1.0.0
## [27] stringr_1.5.1 dplyr_1.1.4
## [29] purrr_1.0.2 readr_2.1.4
## [31] tidyr_1.3.0 tibble_3.2.1
## [33] ggplot2_3.4.4 tidyverse_2.0.0
## [35] zoo_1.8-12 R.utils_2.12.3
## [37] R.oo_1.25.0 R.methodsS3_1.8.2
##
## loaded via a namespace (and not attached):
## [1] bitops_1.0-7 gridExtra_2.3 rlang_1.1.2
## [4] magrittr_2.0.3 compiler_4.3.2 systemfonts_1.0.5
## [7] vctrs_0.6.5 rvest_1.0.3 pkgconfig_2.0.3
## [10] crayon_1.5.2 fastmap_1.1.1 XVector_0.42.0
## [13] ellipsis_0.3.2 caTools_1.18.2 utf8_1.2.4
## [16] promises_1.2.1 rmarkdown_2.25 tzdb_0.4.0
## [19] xfun_0.41 zlibbioc_1.48.0 cachem_1.0.8
## [22] jsonlite_1.8.8 highr_0.10 later_1.3.2
## [25] DelayedArray_0.28.0 BiocParallel_1.36.0 parallel_4.3.2
## [28] R6_2.5.1 bslib_0.6.1 stringi_1.8.3
## [31] RColorBrewer_1.1-3 jquerylib_0.1.4 assertthat_0.2.1
## [34] Rcpp_1.0.11 knitr_1.45 httpuv_1.6.13
## [37] Matrix_1.6-4 timechange_0.2.0 tidyselect_1.2.0
## [40] rstudioapi_0.15.0 abind_1.4-5 yaml_2.3.8
## [43] codetools_0.2-19 lattice_0.22-5 plyr_1.8.9
## [46] shiny_1.8.0 withr_2.5.2 evaluate_0.23
## [49] ggstats_0.5.1 xml2_1.3.6 pillar_1.9.0
## [52] KernSmooth_2.23-22 generics_0.1.3 RCurl_1.98-1.13
## [55] hms_1.1.3 munsell_0.5.0 scales_1.3.0
## [58] xtable_1.8-4 glue_1.6.2 tools_4.3.2
## [61] data.table_1.14.10 webshot_0.5.5 locfit_1.5-9.8
## [64] fastmatch_1.1-4 cowplot_1.1.2 grid_4.3.2
## [67] colorspace_2.1-0 GenomeInfoDbData_1.2.11 cli_3.6.2
## [70] fansi_1.0.6 viridisLite_0.4.2 S4Arrays_1.2.0
## [73] svglite_2.1.3 gtable_0.3.4 sass_0.4.8
## [76] digest_0.6.33 SparseArray_1.2.3 htmlwidgets_1.6.4
## [79] htmltools_0.5.7 lifecycle_1.0.4 httr_1.4.7
## [82] statmod_1.5.0 mime_0.12
END of report