date generated: 2024-03-10
Mitch performs unidimensional and multidimensional gene set enrichment analysis. The concept behind this dates to work by Cox and Mann (https://doi.org/10.1186/1471-2105-13-S16-S12). This implementation is suited to R based workflows of multi-omics datasets. This software was developed by Antony Kaspi and Mark Ziemann. Learn more about Mitch at the website: https://github.com/markziemann/Mitch
Here is the first few lines of the input profile.
x | |
---|---|
A1BG | -0.2987185 |
A1BG-AS1 | -0.4355672 |
A1CF | -0.0075548 |
A2M | 0.2520922 |
A2M-AS1 | -0.8309598 |
A2ML1 | 0.0785158 |
Here are some metrics about the input data profile:
Profile metrics | |
---|---|
num_genesets | 2656 |
num_genes_in_profile | 23030 |
duplicated_genes_present | 0 |
num_profile_genes_in_sets | 10817 |
num_profile_genes_not_in_sets | 12213 |
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_2024-03-10.gmtGene sets metrics | |
---|---|
num_genesets | 2656 |
num_genesets_excluded | 1026 |
num_genesets_included | 1630 |
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 |
---|---|---|---|---|
Fatty acids | 15 | 1.27e-06 | 0.722 | 5.10e-04 |
Eicosanoids | 12 | 5.25e-05 | 0.674 | 7.04e-03 |
Amino Acid conjugation | 9 | 8.38e-04 | 0.643 | 5.62e-02 |
Conjugation of carboxylic acids | 9 | 8.38e-04 | 0.643 | 5.62e-02 |
Conjugation of salicylate with glycine | 8 | 3.00e-03 | 0.606 | 9.74e-02 |
Type I hemidesmosome assembly | 11 | 7.79e-04 | -0.585 | 5.60e-02 |
RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | 8 | 4.46e-03 | 0.581 | 1.18e-01 |
ChREBP activates metabolic gene expression | 8 | 6.85e-03 | -0.552 | 1.55e-01 |
Formyl peptide receptors bind formyl peptides and many other ligands | 8 | 8.24e-03 | 0.539 | 1.67e-01 |
CYP2E1 reactions | 11 | 2.20e-03 | 0.533 | 9.74e-02 |
EGFR interacts with phospholipase C-gamma | 9 | 6.40e-03 | -0.525 | 1.50e-01 |
Mucopolysaccharidoses | 11 | 2.69e-03 | -0.523 | 9.74e-02 |
Pre-NOTCH Processing in the Endoplasmic Reticulum | 6 | 2.71e-02 | -0.521 | 2.90e-01 |
Transport of fatty acids | 8 | 1.16e-02 | -0.515 | 1.99e-01 |
Inhibition of Signaling by Overexpressed EGFR | 8 | 1.22e-02 | -0.512 | 2.06e-01 |
Signaling by Overexpressed Wild-Type EGFR in Cancer | 8 | 1.22e-02 | -0.512 | 2.06e-01 |
Conjugation of benzoate with glycine | 6 | 3.27e-02 | 0.503 | 3.18e-01 |
Sulfide oxidation to sulfate | 5 | 5.14e-02 | -0.503 | 3.79e-01 |
Expression and translocation of olfactory receptors | 334 | 1.38e-55 | 0.498 | 2.78e-52 |
Nef Mediated CD4 Down-regulation | 9 | 1.10e-02 | -0.490 | 1.95e-01 |
Olfactory Signaling Pathway | 342 | 4.61e-54 | 0.486 | 4.64e-51 |
Reelin signalling pathway | 5 | 6.08e-02 | 0.484 | 3.91e-01 |
Biosynthesis of maresin-like SPMs | 6 | 4.23e-02 | 0.479 | 3.61e-01 |
Beta defensins | 27 | 2.03e-05 | 0.474 | 4.88e-03 |
E2F-enabled inhibition of pre-replication complex formation | 9 | 1.44e-02 | 0.471 | 2.22e-01 |
OAS antiviral response | 9 | 1.49e-02 | -0.469 | 2.23e-01 |
Defective LFNG causes SCDO3 | 5 | 7.27e-02 | -0.463 | 4.25e-01 |
NR1H2 & NR1H3 regulate gene expression linked to triglyceride lipolysis in adipose | 5 | 7.32e-02 | -0.463 | 4.25e-01 |
GRB7 events in ERBB2 signaling | 5 | 7.47e-02 | -0.460 | 4.28e-01 |
Regulation of CDH19 Expression and Function | 7 | 3.52e-02 | -0.460 | 3.27e-01 |
Sema4D mediated inhibition of cell attachment and migration | 8 | 2.56e-02 | -0.456 | 2.83e-01 |
NFE2L2 regulating tumorigenic genes | 11 | 9.18e-03 | -0.454 | 1.81e-01 |
Regulation of gene expression in endocrine-committed (NEUROG3+) progenitor cells | 5 | 7.99e-02 | 0.452 | 4.40e-01 |
Miscellaneous substrates | 12 | 7.46e-03 | 0.446 | 1.65e-01 |
CDC6 association with the ORC:origin complex | 8 | 2.95e-02 | 0.444 | 2.97e-01 |
Defensins | 35 | 5.74e-06 | 0.443 | 1.93e-03 |
Uptake and function of diphtheria toxin | 6 | 6.50e-02 | -0.435 | 4.02e-01 |
Ciprofloxacin ADME | 5 | 9.20e-02 | 0.435 | 4.63e-01 |
GAB1 signalosome | 17 | 1.91e-03 | -0.435 | 9.51e-02 |
Synthesis of Ketone Bodies | 8 | 3.47e-02 | -0.431 | 3.26e-01 |
Arachidonate production from DAG | 5 | 9.50e-02 | -0.431 | 4.69e-01 |
Nef Mediated CD8 Down-regulation | 7 | 5.12e-02 | -0.426 | 3.79e-01 |
Specification of the neural plate border | 16 | 3.43e-03 | 0.422 | 1.03e-01 |
Antimicrobial peptides | 79 | 9.67e-11 | 0.421 | 4.86e-08 |
CLEC7A/inflammasome pathway | 6 | 7.61e-02 | -0.418 | 4.31e-01 |
Activation of the phototransduction cascade | 11 | 1.70e-02 | -0.416 | 2.36e-01 |
Epithelial-Mesenchymal Transition (EMT) during gastrulation | 7 | 6.02e-02 | -0.410 | 3.90e-01 |
Reversible hydration of carbon dioxide | 12 | 1.50e-02 | -0.406 | 2.23e-01 |
Loss of MECP2 binding ability to the NCoR/SMRT complex | 7 | 6.86e-02 | -0.398 | 4.08e-01 |
Negative feedback regulation of MAPK pathway | 6 | 9.22e-02 | -0.397 | 4.63e-01 |
set | setSize | pANOVA | s.dist | p.adjustANOVA |
---|---|---|---|---|
Fatty acids | 15 | 1.27e-06 | 7.22e-01 | 5.10e-04 |
Eicosanoids | 12 | 5.25e-05 | 6.74e-01 | 7.04e-03 |
Amino Acid conjugation | 9 | 8.38e-04 | 6.43e-01 | 5.62e-02 |
Conjugation of carboxylic acids | 9 | 8.38e-04 | 6.43e-01 | 5.62e-02 |
Conjugation of salicylate with glycine | 8 | 3.00e-03 | 6.06e-01 | 9.74e-02 |
Type I hemidesmosome assembly | 11 | 7.79e-04 | -5.85e-01 | 5.60e-02 |
RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | 8 | 4.46e-03 | 5.81e-01 | 1.18e-01 |
ChREBP activates metabolic gene expression | 8 | 6.85e-03 | -5.52e-01 | 1.55e-01 |
Formyl peptide receptors bind formyl peptides and many other ligands | 8 | 8.24e-03 | 5.39e-01 | 1.67e-01 |
CYP2E1 reactions | 11 | 2.20e-03 | 5.33e-01 | 9.74e-02 |
EGFR interacts with phospholipase C-gamma | 9 | 6.40e-03 | -5.25e-01 | 1.50e-01 |
Mucopolysaccharidoses | 11 | 2.69e-03 | -5.23e-01 | 9.74e-02 |
Pre-NOTCH Processing in the Endoplasmic Reticulum | 6 | 2.71e-02 | -5.21e-01 | 2.90e-01 |
Transport of fatty acids | 8 | 1.16e-02 | -5.15e-01 | 1.99e-01 |
Inhibition of Signaling by Overexpressed EGFR | 8 | 1.22e-02 | -5.12e-01 | 2.06e-01 |
Signaling by Overexpressed Wild-Type EGFR in Cancer | 8 | 1.22e-02 | -5.12e-01 | 2.06e-01 |
Conjugation of benzoate with glycine | 6 | 3.27e-02 | 5.03e-01 | 3.18e-01 |
Sulfide oxidation to sulfate | 5 | 5.14e-02 | -5.03e-01 | 3.79e-01 |
Expression and translocation of olfactory receptors | 334 | 1.38e-55 | 4.98e-01 | 2.78e-52 |
Nef Mediated CD4 Down-regulation | 9 | 1.10e-02 | -4.90e-01 | 1.95e-01 |
Olfactory Signaling Pathway | 342 | 4.61e-54 | 4.86e-01 | 4.64e-51 |
Reelin signalling pathway | 5 | 6.08e-02 | 4.84e-01 | 3.91e-01 |
Biosynthesis of maresin-like SPMs | 6 | 4.23e-02 | 4.79e-01 | 3.61e-01 |
Beta defensins | 27 | 2.03e-05 | 4.74e-01 | 4.88e-03 |
E2F-enabled inhibition of pre-replication complex formation | 9 | 1.44e-02 | 4.71e-01 | 2.22e-01 |
OAS antiviral response | 9 | 1.49e-02 | -4.69e-01 | 2.23e-01 |
Defective LFNG causes SCDO3 | 5 | 7.27e-02 | -4.63e-01 | 4.25e-01 |
NR1H2 & NR1H3 regulate gene expression linked to triglyceride lipolysis in adipose | 5 | 7.32e-02 | -4.63e-01 | 4.25e-01 |
GRB7 events in ERBB2 signaling | 5 | 7.47e-02 | -4.60e-01 | 4.28e-01 |
Regulation of CDH19 Expression and Function | 7 | 3.52e-02 | -4.60e-01 | 3.27e-01 |
Sema4D mediated inhibition of cell attachment and migration | 8 | 2.56e-02 | -4.56e-01 | 2.83e-01 |
NFE2L2 regulating tumorigenic genes | 11 | 9.18e-03 | -4.54e-01 | 1.81e-01 |
Regulation of gene expression in endocrine-committed (NEUROG3+) progenitor cells | 5 | 7.99e-02 | 4.52e-01 | 4.40e-01 |
Miscellaneous substrates | 12 | 7.46e-03 | 4.46e-01 | 1.65e-01 |
CDC6 association with the ORC:origin complex | 8 | 2.95e-02 | 4.44e-01 | 2.97e-01 |
Defensins | 35 | 5.74e-06 | 4.43e-01 | 1.93e-03 |
Uptake and function of diphtheria toxin | 6 | 6.50e-02 | -4.35e-01 | 4.02e-01 |
Ciprofloxacin ADME | 5 | 9.20e-02 | 4.35e-01 | 4.63e-01 |
GAB1 signalosome | 17 | 1.91e-03 | -4.35e-01 | 9.51e-02 |
Synthesis of Ketone Bodies | 8 | 3.47e-02 | -4.31e-01 | 3.26e-01 |
Arachidonate production from DAG | 5 | 9.50e-02 | -4.31e-01 | 4.69e-01 |
Nef Mediated CD8 Down-regulation | 7 | 5.12e-02 | -4.26e-01 | 3.79e-01 |
Specification of the neural plate border | 16 | 3.43e-03 | 4.22e-01 | 1.03e-01 |
Antimicrobial peptides | 79 | 9.67e-11 | 4.21e-01 | 4.86e-08 |
CLEC7A/inflammasome pathway | 6 | 7.61e-02 | -4.18e-01 | 4.31e-01 |
Activation of the phototransduction cascade | 11 | 1.70e-02 | -4.16e-01 | 2.36e-01 |
Epithelial-Mesenchymal Transition (EMT) during gastrulation | 7 | 6.02e-02 | -4.10e-01 | 3.90e-01 |
Reversible hydration of carbon dioxide | 12 | 1.50e-02 | -4.06e-01 | 2.23e-01 |
Loss of MECP2 binding ability to the NCoR/SMRT complex | 7 | 6.86e-02 | -3.98e-01 | 4.08e-01 |
Negative feedback regulation of MAPK pathway | 6 | 9.22e-02 | -3.97e-01 | 4.63e-01 |
Estrogen-stimulated signaling through PRKCZ | 6 | 9.41e-02 | -3.95e-01 | 4.69e-01 |
RHO GTPases activate KTN1 | 11 | 2.42e-02 | -3.92e-01 | 2.77e-01 |
Signaling by MST1 | 5 | 1.29e-01 | -3.92e-01 | 5.13e-01 |
Activation of RAC1 downstream of NMDARs | 7 | 7.38e-02 | -3.90e-01 | 4.26e-01 |
G2 Phase | 5 | 1.32e-01 | 3.89e-01 | 5.14e-01 |
Biosynthesis of maresins | 8 | 5.73e-02 | 3.88e-01 | 3.90e-01 |
Release of apoptotic factors from the mitochondria | 6 | 1.01e-01 | -3.86e-01 | 4.79e-01 |
Ketone body metabolism | 10 | 3.55e-02 | -3.84e-01 | 3.27e-01 |
Prednisone ADME | 10 | 3.63e-02 | 3.82e-01 | 3.33e-01 |
MECP2 regulates transcription factors | 5 | 1.39e-01 | 3.82e-01 | 5.29e-01 |
Sema4D induced cell migration and growth-cone collapse | 20 | 3.11e-03 | -3.82e-01 | 9.91e-02 |
Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) | 9 | 4.76e-02 | 3.81e-01 | 3.68e-01 |
Apoptotic cleavage of cell adhesion proteins | 11 | 2.88e-02 | -3.81e-01 | 2.93e-01 |
GRB2 events in EGFR signaling | 13 | 1.76e-02 | -3.80e-01 | 2.36e-01 |
RORA activates gene expression | 18 | 5.23e-03 | -3.80e-01 | 1.31e-01 |
MAPK1 (ERK2) activation | 9 | 4.87e-02 | -3.79e-01 | 3.70e-01 |
PP2A-mediated dephosphorylation of key metabolic factors | 7 | 8.38e-02 | -3.77e-01 | 4.50e-01 |
Regulation of CDH11 mRNA translation by microRNAs | 11 | 3.13e-02 | -3.75e-01 | 3.09e-01 |
Metal sequestration by antimicrobial proteins | 6 | 1.12e-01 | 3.74e-01 | 4.95e-01 |
CD28 dependent PI3K/Akt signaling | 22 | 2.40e-03 | -3.74e-01 | 9.74e-02 |
IRAK2 mediated activation of TAK1 complex | 10 | 4.17e-02 | 3.72e-01 | 3.61e-01 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 14 | 1.62e-02 | -3.71e-01 | 2.32e-01 |
APOBEC3G mediated resistance to HIV-1 infection | 5 | 1.54e-01 | 3.68e-01 | 5.54e-01 |
AKT phosphorylates targets in the nucleus | 10 | 4.62e-02 | -3.64e-01 | 3.67e-01 |
Sphingolipid catabolism | 12 | 2.95e-02 | -3.63e-01 | 2.97e-01 |
Sema4D in semaphorin signaling | 24 | 2.15e-03 | -3.62e-01 | 9.74e-02 |
Chylomicron remodeling | 10 | 4.76e-02 | -3.62e-01 | 3.68e-01 |
Negative regulation of TCF-dependent signaling by DVL-interacting proteins | 5 | 1.64e-01 | -3.59e-01 | 5.77e-01 |
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 14 | 2.19e-02 | -3.54e-01 | 2.66e-01 |
Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 24 | 2.71e-03 | -3.54e-01 | 9.74e-02 |
Vitamin C (ascorbate) metabolism | 8 | 8.33e-02 | -3.54e-01 | 4.50e-01 |
IRF3 mediated activation of type 1 IFN | 5 | 1.72e-01 | 3.53e-01 | 5.89e-01 |
Regulation of TP53 Activity through Association with Co-factors | 14 | 2.42e-02 | -3.48e-01 | 2.77e-01 |
Synthesis of PI | 5 | 1.80e-01 | -3.46e-01 | 5.95e-01 |
CDH11 homotypic and heterotypic interactions | 7 | 1.16e-01 | -3.43e-01 | 4.98e-01 |
Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | 8 | 9.37e-02 | -3.42e-01 | 4.68e-01 |
NGF-independant TRKA activation | 5 | 1.85e-01 | 3.42e-01 | 6.01e-01 |
Erythropoietin activates STAT5 | 7 | 1.18e-01 | -3.41e-01 | 5.00e-01 |
Gamma-carboxylation of protein precursors | 9 | 7.70e-02 | -3.40e-01 | 4.34e-01 |
TNFR1-induced proapoptotic signaling | 25 | 3.32e-03 | -3.39e-01 | 1.01e-01 |
Hydrolysis of LPC | 9 | 7.88e-02 | -3.38e-01 | 4.38e-01 |
Alpha-defensins | 8 | 9.77e-02 | 3.38e-01 | 4.75e-01 |
Activation of TRKA receptors | 6 | 1.52e-01 | 3.38e-01 | 5.54e-01 |
Mitochondrial Uncoupling | 6 | 1.55e-01 | 3.35e-01 | 5.54e-01 |
Activation of caspases through apoptosome-mediated cleavage | 6 | 1.57e-01 | 3.34e-01 | 5.58e-01 |
Fructose catabolism | 5 | 1.97e-01 | -3.33e-01 | 6.07e-01 |
Serotonin receptors | 12 | 4.71e-02 | 3.31e-01 | 3.68e-01 |
NR1H2 & NR1H3 regulate gene expression linked to lipogenesis | 9 | 8.71e-02 | -3.29e-01 | 4.51e-01 |
Synthesis of PG | 8 | 1.07e-01 | -3.29e-01 | 4.90e-01 |
Removal of aminoterminal propeptides from gamma-carboxylated proteins | 9 | 8.89e-02 | -3.27e-01 | 4.56e-01 |
Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | 10 | 7.31e-02 | -3.27e-01 | 4.25e-01 |
Alternative complement activation | 5 | 2.12e-01 | -3.22e-01 | 6.18e-01 |
Highly calcium permeable postsynaptic nicotinic acetylcholine receptors | 11 | 6.55e-02 | 3.21e-01 | 4.04e-01 |
Xenobiotics | 24 | 6.76e-03 | 3.19e-01 | 1.55e-01 |
Regulation of TP53 Activity through Acetylation | 29 | 2.92e-03 | -3.19e-01 | 9.74e-02 |
Molybdenum cofactor biosynthesis | 6 | 1.77e-01 | 3.18e-01 | 5.92e-01 |
Caspase activation via Death Receptors in the presence of ligand | 16 | 2.76e-02 | -3.18e-01 | 2.90e-01 |
LDL clearance | 19 | 1.70e-02 | -3.16e-01 | 2.36e-01 |
IL-6-type cytokine receptor ligand interactions | 17 | 2.46e-02 | -3.15e-01 | 2.78e-01 |
Formation of the ureteric bud | 21 | 1.28e-02 | 3.14e-01 | 2.09e-01 |
TRIF-mediated programmed cell death | 9 | 1.04e-01 | -3.13e-01 | 4.85e-01 |
Inactivation of CDC42 and RAC1 | 8 | 1.27e-01 | -3.11e-01 | 5.13e-01 |
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 44 | 3.54e-04 | -3.11e-01 | 3.39e-02 |
Biosynthesis of EPA-derived SPMs | 6 | 1.88e-01 | 3.11e-01 | 6.01e-01 |
Glycosphingolipid transport | 8 | 1.28e-01 | -3.10e-01 | 5.13e-01 |
Regulation of IFNA/IFNB signaling | 20 | 1.64e-02 | 3.10e-01 | 2.32e-01 |
NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis | 9 | 1.07e-01 | -3.10e-01 | 4.91e-01 |
SHC1 events in EGFR signaling | 14 | 4.63e-02 | -3.08e-01 | 3.67e-01 |
Biosynthesis of DHA-derived SPMs | 17 | 2.85e-02 | 3.07e-01 | 2.93e-01 |
RUNX3 regulates WNT signaling | 8 | 1.33e-01 | -3.07e-01 | 5.17e-01 |
Formation of annular gap junctions | 11 | 7.82e-02 | -3.07e-01 | 4.36e-01 |
Regulation of localization of FOXO transcription factors | 12 | 6.60e-02 | -3.07e-01 | 4.04e-01 |
p38MAPK events | 13 | 5.60e-02 | -3.06e-01 | 3.90e-01 |
POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation | 9 | 1.12e-01 | 3.06e-01 | 4.95e-01 |
Adenylate cyclase activating pathway | 10 | 9.56e-02 | -3.04e-01 | 4.70e-01 |
Ligand-receptor interactions | 8 | 1.37e-01 | 3.04e-01 | 5.25e-01 |
Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) | 13 | 5.82e-02 | 3.03e-01 | 3.90e-01 |
Pre-NOTCH Processing in Golgi | 18 | 2.61e-02 | -3.03e-01 | 2.85e-01 |
Displacement of DNA glycosylase by APEX1 | 9 | 1.16e-01 | 3.03e-01 | 4.98e-01 |
FasL/ CD95L signaling | 5 | 2.42e-01 | -3.02e-01 | 6.40e-01 |
HuR (ELAVL1) binds and stabilizes mRNA | 10 | 9.92e-02 | -3.01e-01 | 4.77e-01 |
Regulation of commissural axon pathfinding by SLIT and ROBO | 10 | 9.94e-02 | 3.01e-01 | 4.77e-01 |
NR1H2 and NR1H3-mediated signaling | 54 | 1.37e-04 | -3.00e-01 | 1.62e-02 |
Caspase-mediated cleavage of cytoskeletal proteins | 12 | 7.20e-02 | -3.00e-01 | 4.25e-01 |
Leukotriene receptors | 5 | 2.45e-01 | -3.00e-01 | 6.42e-01 |
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 21 | 1.76e-02 | -2.99e-01 | 2.36e-01 |
PKA activation in glucagon signalling | 17 | 3.29e-02 | -2.99e-01 | 3.19e-01 |
Bicarbonate transporters | 10 | 1.06e-01 | -2.95e-01 | 4.89e-01 |
IRS activation | 5 | 2.53e-01 | -2.95e-01 | 6.48e-01 |
SMAC (DIABLO) binds to IAPs | 7 | 1.78e-01 | 2.94e-01 | 5.92e-01 |
SMAC(DIABLO)-mediated dissociation of IAP:caspase complexes | 7 | 1.78e-01 | 2.94e-01 | 5.92e-01 |
SMAC, XIAP-regulated apoptotic response | 7 | 1.78e-01 | 2.94e-01 | 5.92e-01 |
Repression of WNT target genes | 14 | 5.73e-02 | -2.93e-01 | 3.90e-01 |
TNFR1-mediated ceramide production | 6 | 2.14e-01 | -2.93e-01 | 6.18e-01 |
Downstream signal transduction | 29 | 6.34e-03 | -2.93e-01 | 1.50e-01 |
tRNA processing in the mitochondrion | 5 | 2.58e-01 | 2.92e-01 | 6.51e-01 |
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 12 | 8.11e-02 | -2.91e-01 | 4.43e-01 |
Orexin and neuropeptides FF and QRFP bind to their respective receptors | 8 | 1.55e-01 | -2.90e-01 | 5.54e-01 |
SARS-CoV-2 targets host intracellular signalling and regulatory pathways | 12 | 8.28e-02 | -2.89e-01 | 4.50e-01 |
Signaling by FGFR4 in disease | 11 | 9.69e-02 | -2.89e-01 | 4.74e-01 |
Formation of the anterior neural plate | 10 | 1.14e-01 | 2.88e-01 | 4.97e-01 |
Phosphate bond hydrolysis by NTPDase proteins | 8 | 1.59e-01 | -2.88e-01 | 5.63e-01 |
Pyrimidine salvage | 11 | 9.94e-02 | -2.87e-01 | 4.77e-01 |
Sensory Perception | 558 | 3.61e-31 | 2.87e-01 | 2.42e-28 |
EGFR Transactivation by Gastrin | 9 | 1.36e-01 | -2.87e-01 | 5.25e-01 |
RHO GTPases activate CIT | 19 | 3.06e-02 | -2.87e-01 | 3.03e-01 |
Biosynthesis of specialized proresolving mediators (SPMs) | 19 | 3.06e-02 | 2.86e-01 | 3.03e-01 |
Synthesis of wybutosine at G37 of tRNA(Phe) | 6 | 2.24e-01 | 2.86e-01 | 6.26e-01 |
Defective factor VIII causes hemophilia A | 7 | 1.94e-01 | -2.84e-01 | 6.07e-01 |
Carnitine metabolism | 14 | 6.69e-02 | -2.83e-01 | 4.06e-01 |
Regulation of PTEN mRNA translation | 28 | 9.65e-03 | -2.83e-01 | 1.87e-01 |
Regulation of signaling by NODAL | 9 | 1.43e-01 | -2.82e-01 | 5.37e-01 |
Synthesis of 12-eicosatetraenoic acid derivatives | 7 | 1.96e-01 | -2.82e-01 | 6.07e-01 |
Blood group systems biosynthesis | 22 | 2.22e-02 | -2.82e-01 | 2.66e-01 |
RUNX3 regulates YAP1-mediated transcription | 7 | 2.01e-01 | -2.79e-01 | 6.08e-01 |
IkBA variant leads to EDA-ID | 7 | 2.01e-01 | -2.79e-01 | 6.08e-01 |
LTC4-CYSLTR mediated IL4 production | 7 | 2.05e-01 | -2.77e-01 | 6.08e-01 |
RHO GTPases activate PAKs | 21 | 2.82e-02 | -2.77e-01 | 2.93e-01 |
FBXW7 Mutants and NOTCH1 in Cancer | 5 | 2.85e-01 | -2.76e-01 | 6.76e-01 |
Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling | 5 | 2.85e-01 | -2.76e-01 | 6.76e-01 |
Glucocorticoid biosynthesis | 10 | 1.31e-01 | 2.76e-01 | 5.13e-01 |
Class C/3 (Metabotropic glutamate/pheromone receptors) | 39 | 2.91e-03 | 2.75e-01 | 9.74e-02 |
Synthesis, secretion, and deacylation of Ghrelin | 19 | 4.02e-02 | 2.72e-01 | 3.55e-01 |
Acetylcholine inhibits contraction of outer hair cells | 5 | 2.93e-01 | -2.72e-01 | 6.82e-01 |
Regulation of TNFR1 signaling | 48 | 1.13e-03 | -2.72e-01 | 7.08e-02 |
Role of second messengers in netrin-1 signaling | 10 | 1.37e-01 | 2.71e-01 | 5.25e-01 |
Lewis blood group biosynthesis | 18 | 4.62e-02 | -2.71e-01 | 3.67e-01 |
Smooth Muscle Contraction | 42 | 2.55e-03 | -2.69e-01 | 9.74e-02 |
Organic anion transport | 5 | 3.00e-01 | -2.68e-01 | 6.86e-01 |
Regulation of cytoskeletal remodeling and cell spreading by IPP complex components | 8 | 1.90e-01 | -2.68e-01 | 6.05e-01 |
Signaling by KIT in disease | 20 | 3.84e-02 | -2.67e-01 | 3.43e-01 |
Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 20 | 3.84e-02 | -2.67e-01 | 3.43e-01 |
Glycerophospholipid catabolism | 7 | 2.21e-01 | -2.67e-01 | 6.26e-01 |
NR1H2 & NR1H3 regulate gene expression linked to gluconeogenesis | 5 | 3.01e-01 | -2.67e-01 | 6.87e-01 |
Plasma lipoprotein assembly | 19 | 4.47e-02 | -2.66e-01 | 3.67e-01 |
Polo-like kinase mediated events | 16 | 6.57e-02 | 2.66e-01 | 4.04e-01 |
Gap junction degradation | 12 | 1.12e-01 | -2.65e-01 | 4.95e-01 |
FLT3 signaling by CBL mutants | 7 | 2.26e-01 | 2.64e-01 | 6.26e-01 |
Translesion synthesis by POLK | 17 | 5.99e-02 | 2.64e-01 | 3.90e-01 |
XBP1(S) activates chaperone genes | 44 | 2.57e-03 | -2.63e-01 | 9.74e-02 |
GP1b-IX-V activation signalling | 12 | 1.15e-01 | -2.63e-01 | 4.98e-01 |
HDL assembly | 8 | 1.99e-01 | -2.62e-01 | 6.07e-01 |
Evasion by RSV of host interferon responses | 29 | 1.47e-02 | 2.62e-01 | 2.23e-01 |
SOS-mediated signalling | 7 | 2.32e-01 | -2.61e-01 | 6.31e-01 |
Cytochrome P450 - arranged by substrate type | 65 | 2.82e-04 | 2.60e-01 | 2.88e-02 |
PECAM1 interactions | 12 | 1.19e-01 | -2.60e-01 | 5.00e-01 |
LDL remodeling | 6 | 2.70e-01 | 2.60e-01 | 6.68e-01 |
Platelet sensitization by LDL | 17 | 6.41e-02 | -2.59e-01 | 3.99e-01 |
Cytosolic iron-sulfur cluster assembly | 13 | 1.07e-01 | -2.58e-01 | 4.89e-01 |
Tyrosine catabolism | 5 | 3.17e-01 | -2.58e-01 | 7.03e-01 |
Coenzyme A biosynthesis | 7 | 2.37e-01 | -2.58e-01 | 6.36e-01 |
Interleukin-21 signaling | 10 | 1.58e-01 | -2.58e-01 | 5.61e-01 |
RHOV GTPase cycle | 37 | 6.71e-03 | -2.57e-01 | 1.55e-01 |
ERBB2 Activates PTK6 Signaling | 13 | 1.09e-01 | -2.57e-01 | 4.92e-01 |
Regulation of NFE2L2 gene expression | 8 | 2.10e-01 | -2.56e-01 | 6.15e-01 |
Paracetamol ADME | 27 | 2.16e-02 | -2.55e-01 | 2.66e-01 |
VEGFR2 mediated vascular permeability | 27 | 2.17e-02 | -2.55e-01 | 2.66e-01 |
Degradation of cysteine and homocysteine | 14 | 9.87e-02 | -2.55e-01 | 4.77e-01 |
Sensing of DNA Double Strand Breaks | 6 | 2.80e-01 | 2.55e-01 | 6.74e-01 |
Fructose metabolism | 7 | 2.45e-01 | -2.54e-01 | 6.42e-01 |
Diseases associated with visual transduction | 12 | 1.30e-01 | -2.52e-01 | 5.13e-01 |
Diseases of the neuronal system | 12 | 1.30e-01 | -2.52e-01 | 5.13e-01 |
Retinoid cycle disease events | 12 | 1.30e-01 | -2.52e-01 | 5.13e-01 |
DEx/H-box helicases activate type I IFN and inflammatory cytokines production | 7 | 2.50e-01 | -2.51e-01 | 6.47e-01 |
Pyroptosis | 27 | 2.43e-02 | -2.50e-01 | 2.77e-01 |
Aryl hydrocarbon receptor signalling | 7 | 2.54e-01 | -2.49e-01 | 6.48e-01 |
Translesion synthesis by POLI | 17 | 7.62e-02 | 2.48e-01 | 4.31e-01 |
Translesion synthesis by REV1 | 16 | 8.54e-02 | 2.48e-01 | 4.50e-01 |
NR1H2 & NR1H3 regulate gene expression to limit cholesterol uptake | 5 | 3.37e-01 | -2.48e-01 | 7.12e-01 |
Retrograde neurotrophin signalling | 14 | 1.09e-01 | -2.48e-01 | 4.92e-01 |
Noncanonical activation of NOTCH3 | 8 | 2.25e-01 | -2.48e-01 | 6.26e-01 |
Interleukin-23 signaling | 9 | 1.99e-01 | -2.47e-01 | 6.07e-01 |
Interleukin-9 signaling | 8 | 2.28e-01 | -2.46e-01 | 6.26e-01 |
NGF-stimulated transcription | 39 | 7.93e-03 | 2.46e-01 | 1.67e-01 |
Sodium/Calcium exchangers | 11 | 1.59e-01 | 2.45e-01 | 5.63e-01 |
Notch-HLH transcription pathway | 28 | 2.54e-02 | -2.44e-01 | 2.83e-01 |
IRE1alpha activates chaperones | 46 | 4.28e-03 | -2.43e-01 | 1.15e-01 |
Diseases of Mismatch Repair (MMR) | 5 | 3.48e-01 | 2.42e-01 | 7.17e-01 |
SUMOylation of DNA methylation proteins | 16 | 9.36e-02 | -2.42e-01 | 4.68e-01 |
NTRK2 activates RAC1 | 5 | 3.49e-01 | 2.42e-01 | 7.17e-01 |
Binding of TCF/LEF:CTNNB1 to target gene promoters | 8 | 2.37e-01 | -2.42e-01 | 6.36e-01 |
Tight junction interactions | 29 | 2.46e-02 | -2.41e-01 | 2.78e-01 |
HS-GAG degradation | 24 | 4.14e-02 | -2.41e-01 | 3.60e-01 |
Regulation of RUNX1 Expression and Activity | 26 | 3.38e-02 | -2.40e-01 | 3.22e-01 |
APC truncation mutants have impaired AXIN binding | 14 | 1.21e-01 | -2.39e-01 | 5.00e-01 |
AXIN missense mutants destabilize the destruction complex | 14 | 1.21e-01 | -2.39e-01 | 5.00e-01 |
Signaling by AMER1 mutants | 14 | 1.21e-01 | -2.39e-01 | 5.00e-01 |
Signaling by APC mutants | 14 | 1.21e-01 | -2.39e-01 | 5.00e-01 |
Signaling by AXIN mutants | 14 | 1.21e-01 | -2.39e-01 | 5.00e-01 |
Truncations of AMER1 destabilize the destruction complex | 14 | 1.21e-01 | -2.39e-01 | 5.00e-01 |
tRNA modification in the mitochondrion | 9 | 2.15e-01 | 2.39e-01 | 6.18e-01 |
Highly calcium permeable nicotinic acetylcholine receptors | 9 | 2.15e-01 | 2.39e-01 | 6.18e-01 |
Regulated proteolysis of p75NTR | 11 | 1.70e-01 | -2.39e-01 | 5.87e-01 |
Cell-extracellular matrix interactions | 18 | 7.99e-02 | -2.38e-01 | 4.40e-01 |
NFE2L2 regulating MDR associated enzymes | 8 | 2.45e-01 | -2.37e-01 | 6.42e-01 |
Activation of C3 and C5 | 7 | 2.78e-01 | -2.37e-01 | 6.74e-01 |
APC/C:Cdc20 mediated degradation of Cyclin B | 24 | 4.49e-02 | 2.37e-01 | 3.67e-01 |
WNT mediated activation of DVL | 8 | 2.47e-01 | -2.36e-01 | 6.44e-01 |
POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | 11 | 1.75e-01 | 2.36e-01 | 5.92e-01 |
Activation of PUMA and translocation to mitochondria | 9 | 2.20e-01 | -2.36e-01 | 6.26e-01 |
NrCAM interactions | 7 | 2.80e-01 | -2.36e-01 | 6.74e-01 |
Amine ligand-binding receptors | 42 | 8.18e-03 | 2.36e-01 | 1.67e-01 |
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 14 | 1.27e-01 | -2.35e-01 | 5.13e-01 |
RAF activation | 33 | 1.96e-02 | -2.35e-01 | 2.51e-01 |
Sensory perception of salty taste | 6 | 3.20e-01 | -2.34e-01 | 7.06e-01 |
Activation of Ca-permeable Kainate Receptor | 10 | 2.03e-01 | 2.32e-01 | 6.08e-01 |
Ionotropic activity of kainate receptors | 10 | 2.03e-01 | 2.32e-01 | 6.08e-01 |
HDL clearance | 5 | 3.68e-01 | -2.32e-01 | 7.39e-01 |
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 52 | 3.79e-03 | 2.32e-01 | 1.07e-01 |
p53-Independent DNA Damage Response | 52 | 3.79e-03 | 2.32e-01 | 1.07e-01 |
p53-Independent G1/S DNA damage checkpoint | 52 | 3.79e-03 | 2.32e-01 | 1.07e-01 |
Interleukin-20 family signaling | 26 | 4.06e-02 | -2.32e-01 | 3.56e-01 |
TYSND1 cleaves peroxisomal proteins | 7 | 2.88e-01 | -2.32e-01 | 6.78e-01 |
Glycosphingolipid biosynthesis | 19 | 8.09e-02 | -2.31e-01 | 4.43e-01 |
Interleukin-6 family signaling | 24 | 5.02e-02 | -2.31e-01 | 3.77e-01 |
Glutathione synthesis and recycling | 12 | 1.67e-01 | -2.30e-01 | 5.81e-01 |
Ca2+ activated K+ channels | 9 | 2.32e-01 | -2.30e-01 | 6.31e-01 |
Syndecan interactions | 27 | 3.90e-02 | -2.29e-01 | 3.47e-01 |
Respiratory syncytial virus (RSV) attachment and entry | 23 | 5.70e-02 | -2.29e-01 | 3.90e-01 |
CTNNB1 S33 mutants aren’t phosphorylated | 15 | 1.27e-01 | -2.27e-01 | 5.13e-01 |
CTNNB1 S37 mutants aren’t phosphorylated | 15 | 1.27e-01 | -2.27e-01 | 5.13e-01 |
CTNNB1 S45 mutants aren’t phosphorylated | 15 | 1.27e-01 | -2.27e-01 | 5.13e-01 |
CTNNB1 T41 mutants aren’t phosphorylated | 15 | 1.27e-01 | -2.27e-01 | 5.13e-01 |
Signaling by CTNNB1 phospho-site mutants | 15 | 1.27e-01 | -2.27e-01 | 5.13e-01 |
Signaling by GSK3beta mutants | 15 | 1.27e-01 | -2.27e-01 | 5.13e-01 |
CD28 co-stimulation | 33 | 2.38e-02 | -2.27e-01 | 2.77e-01 |
FCGR activation | 12 | 1.75e-01 | 2.26e-01 | 5.92e-01 |
SUMOylation of immune response proteins | 12 | 1.76e-01 | -2.26e-01 | 5.92e-01 |
Interleukin-1 processing | 9 | 2.41e-01 | -2.25e-01 | 6.40e-01 |
Prolonged ERK activation events | 14 | 1.44e-01 | -2.25e-01 | 5.42e-01 |
Common Pathway of Fibrin Clot Formation | 22 | 6.75e-02 | -2.25e-01 | 4.07e-01 |
Frs2-mediated activation | 12 | 1.77e-01 | -2.25e-01 | 5.92e-01 |
The fatty acid cycling model | 5 | 3.85e-01 | 2.24e-01 | 7.51e-01 |
The proton buffering model | 5 | 3.85e-01 | 2.24e-01 | 7.51e-01 |
Folding of actin by CCT/TriC | 10 | 2.20e-01 | 2.24e-01 | 6.26e-01 |
RUNX1 regulates transcription of genes involved in BCR signaling | 6 | 3.42e-01 | 2.24e-01 | 7.12e-01 |
Acyl chain remodelling of PC | 27 | 4.43e-02 | -2.24e-01 | 3.67e-01 |
Regulation of Expression and Function of Type II Classical Cadherins | 33 | 2.63e-02 | -2.23e-01 | 2.85e-01 |
Regulation of Homotypic Cell-Cell Adhesion | 33 | 2.63e-02 | -2.23e-01 | 2.85e-01 |
APEX1-Independent Resolution of AP Sites via the Single Nucleotide Replacement Pathway | 7 | 3.09e-01 | -2.22e-01 | 6.97e-01 |
Signaling by EGFR | 53 | 5.15e-03 | -2.22e-01 | 1.31e-01 |
Biosynthesis of E-series 18(S)-resolvins | 5 | 3.91e-01 | 2.21e-01 | 7.54e-01 |
Impaired BRCA2 binding to PALB2 | 24 | 6.05e-02 | 2.21e-01 | 3.90e-01 |
Tandem pore domain potassium channels | 12 | 1.86e-01 | 2.20e-01 | 6.01e-01 |
Defective HLCS causes multiple carboxylase deficiency | 7 | 3.13e-01 | -2.20e-01 | 7.02e-01 |
IFNG signaling activates MAPKs | 8 | 2.82e-01 | -2.20e-01 | 6.76e-01 |
Phase 1 - inactivation of fast Na+ channels | 7 | 3.15e-01 | 2.20e-01 | 7.03e-01 |
Maturation of protein 3a 9683673 | 9 | 2.54e-01 | -2.19e-01 | 6.48e-01 |
Maturation of protein 3a 9694719 | 9 | 2.54e-01 | -2.19e-01 | 6.48e-01 |
Defective F9 activation | 6 | 3.54e-01 | 2.19e-01 | 7.19e-01 |
TLR3-mediated TICAM1-dependent programmed cell death | 6 | 3.54e-01 | -2.19e-01 | 7.19e-01 |
Pregnenolone biosynthesis | 12 | 1.92e-01 | -2.17e-01 | 6.07e-01 |
Regulation of gene expression in early pancreatic precursor cells | 8 | 2.87e-01 | 2.17e-01 | 6.77e-01 |
TP53 Regulates Transcription of Death Receptors and Ligands | 12 | 1.93e-01 | -2.17e-01 | 6.07e-01 |
CTLA4 inhibitory signaling | 21 | 8.52e-02 | -2.17e-01 | 4.50e-01 |
Regulation of CDH11 Expression and Function | 30 | 4.01e-02 | -2.17e-01 | 3.55e-01 |
FGFR3b ligand binding and activation | 7 | 3.22e-01 | -2.16e-01 | 7.06e-01 |
CASP8 activity is inhibited | 11 | 2.15e-01 | -2.16e-01 | 6.18e-01 |
Dimerization of procaspase-8 | 11 | 2.15e-01 | -2.16e-01 | 6.18e-01 |
Regulation by c-FLIP | 11 | 2.15e-01 | -2.16e-01 | 6.18e-01 |
Hh mutants are degraded by ERAD | 56 | 5.22e-03 | 2.16e-01 | 1.31e-01 |
Histidine catabolism | 8 | 2.92e-01 | -2.15e-01 | 6.82e-01 |
HDL remodeling | 10 | 2.39e-01 | -2.15e-01 | 6.39e-01 |
Chylomicron assembly | 10 | 2.39e-01 | -2.15e-01 | 6.39e-01 |
CD163 mediating an anti-inflammatory response | 9 | 2.65e-01 | -2.14e-01 | 6.62e-01 |
TNF signaling | 57 | 5.20e-03 | -2.14e-01 | 1.31e-01 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 13 | 1.83e-01 | -2.13e-01 | 5.97e-01 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 128 | 3.04e-05 | 2.13e-01 | 5.09e-03 |
Prolactin receptor signaling | 15 | 1.53e-01 | -2.13e-01 | 5.54e-01 |
APC/C:Cdc20 mediated degradation of mitotic proteins | 76 | 1.34e-03 | 2.13e-01 | 7.68e-02 |
Synthesis of bile acids and bile salts via 24-hydroxycholesterol | 14 | 1.68e-01 | 2.13e-01 | 5.84e-01 |
SUMO is conjugated to E1 (UBA2:SAE1) | 5 | 4.10e-01 | 2.13e-01 | 7.67e-01 |
Chylomicron clearance | 5 | 4.10e-01 | -2.13e-01 | 7.67e-01 |
PI3K events in ERBB2 signaling | 16 | 1.41e-01 | -2.12e-01 | 5.35e-01 |
Vitamins | 6 | 3.68e-01 | 2.12e-01 | 7.39e-01 |
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 77 | 1.31e-03 | 2.12e-01 | 7.68e-02 |
NOTCH4 Intracellular Domain Regulates Transcription | 20 | 1.01e-01 | -2.12e-01 | 4.79e-01 |
Defective CFTR causes cystic fibrosis | 61 | 4.27e-03 | 2.12e-01 | 1.15e-01 |
Plasma lipoprotein clearance | 37 | 2.62e-02 | -2.11e-01 | 2.85e-01 |
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | 25 | 6.85e-02 | 2.10e-01 | 4.08e-01 |
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | 25 | 6.85e-02 | 2.10e-01 | 4.08e-01 |
Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 25 | 6.85e-02 | 2.10e-01 | 4.08e-01 |
Defective homologous recombination repair (HRR) due to PALB2 loss of function | 25 | 6.85e-02 | 2.10e-01 | 4.08e-01 |
Beta-oxidation of very long chain fatty acids | 11 | 2.28e-01 | -2.10e-01 | 6.26e-01 |
The role of Nef in HIV-1 replication and disease pathogenesis | 28 | 5.48e-02 | -2.10e-01 | 3.87e-01 |
Constitutive Signaling by NOTCH1 t(7;9)(NOTCH1:M1580 K2555) Translocation Mutant | 7 | 3.38e-01 | -2.09e-01 | 7.12e-01 |
Signaling by NOTCH1 t(7;9)(NOTCH1:M1580 K2555) Translocation Mutant | 7 | 3.38e-01 | -2.09e-01 | 7.12e-01 |
Sodium-coupled phosphate cotransporters | 5 | 4.18e-01 | -2.09e-01 | 7.69e-01 |
Defective C1GALT1C1 causes TNPS | 19 | 1.15e-01 | 2.09e-01 | 4.98e-01 |
APC/C:Cdc20 mediated degradation of Securin | 68 | 2.89e-03 | 2.09e-01 | 9.74e-02 |
rRNA modification in the mitochondrion | 6 | 3.77e-01 | -2.08e-01 | 7.47e-01 |
RHOU GTPase cycle | 40 | 2.27e-02 | -2.08e-01 | 2.68e-01 |
RUNX1 regulates transcription of genes involved in WNT signaling | 6 | 3.77e-01 | 2.08e-01 | 7.47e-01 |
Synthesis of Leukotrienes (LT) and Eoxins (EX) | 21 | 9.87e-02 | 2.08e-01 | 4.77e-01 |
Establishment of Sister Chromatid Cohesion | 11 | 2.32e-01 | 2.08e-01 | 6.31e-01 |
Formation of lateral plate mesoderm | 5 | 4.21e-01 | 2.08e-01 | 7.69e-01 |
Nuclear events stimulated by ALK signaling in cancer | 35 | 3.34e-02 | -2.08e-01 | 3.22e-01 |
CREB phosphorylation | 7 | 3.41e-01 | 2.08e-01 | 7.12e-01 |
AUF1 (hnRNP D0) binds and destabilizes mRNA | 55 | 7.79e-03 | 2.07e-01 | 1.67e-01 |
DNA methylation | 28 | 5.77e-02 | -2.07e-01 | 3.90e-01 |
G2/M DNA replication checkpoint | 5 | 4.22e-01 | 2.07e-01 | 7.69e-01 |
Interleukin-36 pathway | 7 | 3.43e-01 | 2.07e-01 | 7.12e-01 |
Ubiquitin-dependent degradation of Cyclin D | 52 | 1.00e-02 | 2.06e-01 | 1.92e-01 |
Acyl chain remodelling of PE | 29 | 5.44e-02 | -2.06e-01 | 3.87e-01 |
Activated NTRK2 signals through RAS | 9 | 2.85e-01 | 2.06e-01 | 6.76e-01 |
Disorders of Developmental Biology | 13 | 1.99e-01 | -2.06e-01 | 6.07e-01 |
Disorders of Nervous System Development | 13 | 1.99e-01 | -2.06e-01 | 6.07e-01 |
Loss of function of MECP2 in Rett syndrome | 13 | 1.99e-01 | -2.06e-01 | 6.07e-01 |
Pervasive developmental disorders | 13 | 1.99e-01 | -2.06e-01 | 6.07e-01 |
Activation of BAD and translocation to mitochondria | 15 | 1.68e-01 | -2.06e-01 | 5.84e-01 |
Loss of Function of SMAD2/3 in Cancer | 7 | 3.46e-01 | 2.06e-01 | 7.16e-01 |
CDK-mediated phosphorylation and removal of Cdc6 | 73 | 2.43e-03 | 2.05e-01 | 9.74e-02 |
Activation of gene expression by SREBF (SREBP) | 42 | 2.15e-02 | -2.05e-01 | 2.66e-01 |
Orc1 removal from chromatin | 71 | 2.83e-03 | 2.05e-01 | 9.74e-02 |
CHL1 interactions | 9 | 2.89e-01 | 2.04e-01 | 6.79e-01 |
Stabilization of p53 | 56 | 8.32e-03 | 2.04e-01 | 1.67e-01 |
Regulation of activated PAK-2p34 by proteasome mediated degradation | 50 | 1.27e-02 | 2.04e-01 | 2.09e-01 |
BMAL1:CLOCK,NPAS2 activates circadian gene expression | 25 | 7.82e-02 | -2.03e-01 | 4.36e-01 |
Signaling by NTRK3 (TRKC) | 17 | 1.47e-01 | -2.03e-01 | 5.46e-01 |
Pre-NOTCH Expression and Processing | 84 | 1.32e-03 | -2.03e-01 | 7.68e-02 |
Zinc efflux and compartmentalization by the SLC30 family | 5 | 4.33e-01 | 2.02e-01 | 7.77e-01 |
Disinhibition of SNARE formation | 5 | 4.35e-01 | 2.02e-01 | 7.77e-01 |
Semaphorin interactions | 64 | 5.28e-03 | -2.02e-01 | 1.31e-01 |
Vif-mediated degradation of APOBEC3G | 54 | 1.04e-02 | 2.02e-01 | 1.93e-01 |
Thrombin signalling through proteinase activated receptors (PARs) | 32 | 4.84e-02 | -2.02e-01 | 3.69e-01 |
Signal attenuation | 10 | 2.71e-01 | -2.01e-01 | 6.68e-01 |
Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 73 | 2.96e-03 | 2.01e-01 | 9.74e-02 |
Autodegradation of the E3 ubiquitin ligase COP1 | 51 | 1.31e-02 | 2.01e-01 | 2.10e-01 |
Synthesis of 5-eicosatetraenoic acids | 9 | 2.97e-01 | 2.01e-01 | 6.84e-01 |
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 74 | 2.86e-03 | 2.00e-01 | 9.74e-02 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 14 | 1.95e-01 | -2.00e-01 | 6.07e-01 |
Defective EXT2 causes exostoses 2 | 14 | 1.95e-01 | -2.00e-01 | 6.07e-01 |
Other semaphorin interactions | 19 | 1.31e-01 | -2.00e-01 | 5.13e-01 |
BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members | 9 | 3.00e-01 | -2.00e-01 | 6.86e-01 |
Hh mutants abrogate ligand secretion | 59 | 8.07e-03 | 1.99e-01 | 1.67e-01 |
Intrinsic Pathway for Apoptosis | 54 | 1.13e-02 | -1.99e-01 | 1.97e-01 |
Lysine catabolism | 12 | 2.32e-01 | 1.99e-01 | 6.31e-01 |
Adenylate cyclase inhibitory pathway | 14 | 1.98e-01 | -1.99e-01 | 6.07e-01 |
Activation of the pre-replicative complex | 33 | 4.85e-02 | 1.98e-01 | 3.69e-01 |
Eicosanoid ligand-binding receptors | 15 | 1.84e-01 | -1.98e-01 | 5.98e-01 |
TNFR1-induced NF-kappa-B signaling pathway | 33 | 4.89e-02 | -1.98e-01 | 3.70e-01 |
Metabolism of ingested SeMet, Sec, MeSec into H2Se | 8 | 3.35e-01 | -1.97e-01 | 7.12e-01 |
Cell junction organization | 117 | 2.36e-04 | -1.97e-01 | 2.63e-02 |
Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 21 | 1.20e-01 | 1.96e-01 | 5.00e-01 |
Defective RIPK1-mediated regulated necrosis | 7 | 3.70e-01 | -1.96e-01 | 7.40e-01 |
PKA activation | 18 | 1.51e-01 | -1.96e-01 | 5.54e-01 |
Regulation of Apoptosis | 53 | 1.39e-02 | 1.95e-01 | 2.18e-01 |
TBC/RABGAPs | 44 | 2.51e-02 | -1.95e-01 | 2.82e-01 |
Diseases of carbohydrate metabolism | 33 | 5.27e-02 | -1.95e-01 | 3.83e-01 |
Translesion Synthesis by POLH | 18 | 1.52e-01 | 1.95e-01 | 5.54e-01 |
Phosphorylation of Emi1 | 6 | 4.09e-01 | 1.95e-01 | 7.67e-01 |
MAPK3 (ERK1) activation | 10 | 2.87e-01 | -1.95e-01 | 6.77e-01 |
Terminal pathway of complement | 8 | 3.41e-01 | 1.94e-01 | 7.12e-01 |
APC-Cdc20 mediated degradation of Nek2A | 26 | 8.65e-02 | 1.94e-01 | 4.51e-01 |
Estrogen biosynthesis | 6 | 4.12e-01 | -1.94e-01 | 7.67e-01 |
MET activates PTPN11 | 5 | 4.54e-01 | 1.93e-01 | 7.88e-01 |
G1/S DNA Damage Checkpoints | 67 | 6.27e-03 | 1.93e-01 | 1.50e-01 |
Choline catabolism | 6 | 4.13e-01 | -1.93e-01 | 7.67e-01 |
Asymmetric localization of PCP proteins | 64 | 7.60e-03 | 1.93e-01 | 1.66e-01 |
Post-transcriptional silencing by small RNAs | 7 | 3.77e-01 | -1.93e-01 | 7.47e-01 |
Netrin mediated repulsion signals | 8 | 3.45e-01 | 1.93e-01 | 7.15e-01 |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 74 | 4.18e-03 | 1.93e-01 | 1.15e-01 |
Degradation of AXIN | 55 | 1.35e-02 | 1.93e-01 | 2.14e-01 |
NOTCH3 Intracellular Domain Regulates Transcription | 25 | 9.57e-02 | -1.93e-01 | 4.70e-01 |
SUMO is proteolytically processed | 6 | 4.15e-01 | 1.92e-01 | 7.67e-01 |
Integrin signaling | 27 | 8.40e-02 | -1.92e-01 | 4.50e-01 |
Striated Muscle Contraction | 36 | 4.61e-02 | -1.92e-01 | 3.67e-01 |
SCF(Skp2)-mediated degradation of p27/p21 | 60 | 1.02e-02 | 1.92e-01 | 1.93e-01 |
Switching of origins to a post-replicative state | 92 | 1.53e-03 | 1.91e-01 | 8.01e-02 |
WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 13 | 2.33e-01 | -1.91e-01 | 6.31e-01 |
RHO GTPases Activate Rhotekin and Rhophilins | 9 | 3.21e-01 | -1.91e-01 | 7.06e-01 |
Activation of ATR in response to replication stress | 37 | 4.47e-02 | 1.91e-01 | 3.67e-01 |
SMAD2/3 Phosphorylation Motif Mutants in Cancer | 6 | 4.19e-01 | 1.91e-01 | 7.69e-01 |
TGFBR1 KD Mutants in Cancer | 6 | 4.19e-01 | 1.91e-01 | 7.69e-01 |
TRAF6 mediated IRF7 activation | 24 | 1.06e-01 | 1.90e-01 | 4.89e-01 |
Signaling by TGF-beta Receptor Complex in Cancer | 8 | 3.51e-01 | 1.90e-01 | 7.17e-01 |
STAT5 Activation | 7 | 3.83e-01 | -1.90e-01 | 7.51e-01 |
Recycling of eIF2:GDP | 8 | 3.52e-01 | 1.90e-01 | 7.18e-01 |
Signaling by NODAL | 20 | 1.42e-01 | -1.90e-01 | 5.35e-01 |
Anchoring fibril formation | 15 | 2.04e-01 | -1.89e-01 | 6.08e-01 |
Telomere C-strand synthesis initiation | 13 | 2.38e-01 | 1.89e-01 | 6.37e-01 |
Adrenoceptors | 9 | 3.26e-01 | 1.89e-01 | 7.07e-01 |
Pre-NOTCH Transcription and Translation | 68 | 7.07e-03 | -1.89e-01 | 1.58e-01 |
Platelet Aggregation (Plug Formation) | 39 | 4.18e-02 | -1.88e-01 | 3.61e-01 |
Phosphorylation of the APC/C | 20 | 1.45e-01 | 1.88e-01 | 5.42e-01 |
TP53 Regulates Transcription of Caspase Activators and Caspases | 12 | 2.60e-01 | -1.88e-01 | 6.53e-01 |
GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 52 | 1.91e-02 | 1.88e-01 | 2.47e-01 |
APC/C-mediated degradation of cell cycle proteins | 88 | 2.33e-03 | 1.88e-01 | 9.74e-02 |
Regulation of mitotic cell cycle | 88 | 2.33e-03 | 1.88e-01 | 9.74e-02 |
Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 13 | 2.41e-01 | 1.88e-01 | 6.40e-01 |
Electric Transmission Across Gap Junctions | 5 | 4.69e-01 | 1.87e-01 | 7.95e-01 |
Transmission across Electrical Synapses | 5 | 4.69e-01 | 1.87e-01 | 7.95e-01 |
Signalling to ERKs | 34 | 5.94e-02 | -1.87e-01 | 3.90e-01 |
Glucagon signaling in metabolic regulation | 32 | 6.74e-02 | -1.87e-01 | 4.07e-01 |
Regulation of CDH11 gene transcription | 10 | 3.06e-01 | -1.87e-01 | 6.93e-01 |
Regulation of APC/C activators between G1/S and early anaphase | 81 | 3.66e-03 | 1.87e-01 | 1.07e-01 |
Alpha-protein kinase 1 signaling pathway | 11 | 2.84e-01 | 1.87e-01 | 6.76e-01 |
TICAM1,TRAF6-dependent induction of TAK1 complex | 11 | 2.84e-01 | 1.87e-01 | 6.76e-01 |
DNA Damage Reversal | 8 | 3.61e-01 | -1.86e-01 | 7.30e-01 |
Constitutive Signaling by AKT1 E17K in Cancer | 26 | 1.01e-01 | -1.86e-01 | 4.79e-01 |
Interleukin-2 family signaling | 40 | 4.22e-02 | -1.86e-01 | 3.61e-01 |
VLDL assembly | 5 | 4.72e-01 | -1.86e-01 | 7.97e-01 |
SCF-beta-TrCP mediated degradation of Emi1 | 55 | 1.76e-02 | 1.85e-01 | 2.36e-01 |
Modulation by Mtb of host immune system | 6 | 4.33e-01 | 1.85e-01 | 7.77e-01 |
TP53 Regulates Transcription of Cell Death Genes | 44 | 3.38e-02 | -1.85e-01 | 3.22e-01 |
NOSTRIN mediated eNOS trafficking | 5 | 4.75e-01 | 1.85e-01 | 7.99e-01 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 39 | 4.63e-02 | -1.84e-01 | 3.67e-01 |
Peroxisomal lipid metabolism | 29 | 8.60e-02 | -1.84e-01 | 4.50e-01 |
Aspirin ADME | 41 | 4.14e-02 | 1.84e-01 | 3.60e-01 |
Opsins | 8 | 3.67e-01 | -1.84e-01 | 7.39e-01 |
Chemokine receptors bind chemokines | 56 | 1.73e-02 | 1.84e-01 | 2.36e-01 |
Vpu mediated degradation of CD4 | 52 | 2.18e-02 | 1.84e-01 | 2.66e-01 |
P2Y receptors | 12 | 2.70e-01 | -1.84e-01 | 6.68e-01 |
p53-Dependent G1 DNA Damage Response | 65 | 1.05e-02 | 1.84e-01 | 1.93e-01 |
p53-Dependent G1/S DNA damage checkpoint | 65 | 1.05e-02 | 1.84e-01 | 1.93e-01 |
Autodegradation of Cdh1 by Cdh1:APC/C | 64 | 1.11e-02 | 1.84e-01 | 1.96e-01 |
Non-integrin membrane-ECM interactions | 59 | 1.51e-02 | -1.83e-01 | 2.24e-01 |
Degradation of DVL | 57 | 1.71e-02 | 1.83e-01 | 2.36e-01 |
Formation of the posterior neural plate | 10 | 3.18e-01 | 1.82e-01 | 7.03e-01 |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane | 11 | 2.97e-01 | -1.82e-01 | 6.84e-01 |
Nucleotide-like (purinergic) receptors | 16 | 2.09e-01 | -1.81e-01 | 6.14e-01 |
Digestion of dietary lipid | 7 | 4.07e-01 | 1.81e-01 | 7.67e-01 |
Melanin biosynthesis | 5 | 4.85e-01 | 1.80e-01 | 8.03e-01 |
Death Receptor Signaling | 154 | 1.13e-04 | -1.80e-01 | 1.43e-02 |
RHOB GTPase cycle | 69 | 9.69e-03 | -1.80e-01 | 1.87e-01 |
Cell recruitment (pro-inflammatory response) | 26 | 1.12e-01 | -1.80e-01 | 4.95e-01 |
Purinergic signaling in leishmaniasis infection | 26 | 1.12e-01 | -1.80e-01 | 4.95e-01 |
Regulation of cholesterol biosynthesis by SREBP (SREBF) | 55 | 2.11e-02 | -1.80e-01 | 2.66e-01 |
PI3K/AKT activation | 9 | 3.50e-01 | -1.80e-01 | 7.17e-01 |
Dectin-2 family | 28 | 9.97e-02 | 1.80e-01 | 4.77e-01 |
Signaling by cytosolic FGFR1 fusion mutants | 18 | 1.88e-01 | -1.79e-01 | 6.01e-01 |
Neurofascin interactions | 7 | 4.13e-01 | 1.79e-01 | 7.67e-01 |
RHO GTPases Activate ROCKs | 19 | 1.78e-01 | -1.79e-01 | 5.92e-01 |
Phenylalanine and tyrosine metabolism | 11 | 3.05e-01 | -1.79e-01 | 6.91e-01 |
NRAGE signals death through JNK | 58 | 1.86e-02 | -1.79e-01 | 2.43e-01 |
RIP-mediated NFkB activation via ZBP1 | 17 | 2.04e-01 | -1.78e-01 | 6.08e-01 |
VEGFA-VEGFR2 Pathway | 97 | 2.49e-03 | -1.78e-01 | 9.74e-02 |
Signaling by ERBB2 ECD mutants | 16 | 2.19e-01 | -1.78e-01 | 6.26e-01 |
GRB2 events in ERBB2 signaling | 16 | 2.19e-01 | -1.77e-01 | 6.26e-01 |
DNA replication initiation | 8 | 3.85e-01 | 1.77e-01 | 7.51e-01 |
Advanced glycosylation endproduct receptor signaling | 13 | 2.69e-01 | -1.77e-01 | 6.68e-01 |
Cross-presentation of soluble exogenous antigens (endosomes) | 48 | 3.45e-02 | 1.76e-01 | 3.25e-01 |
Nicotinate metabolism | 31 | 8.95e-02 | -1.76e-01 | 4.58e-01 |
Growth hormone receptor signaling | 24 | 1.36e-01 | -1.76e-01 | 5.25e-01 |
Loss of Function of TGFBR1 in Cancer | 7 | 4.22e-01 | 1.75e-01 | 7.69e-01 |
Activation of BH3-only proteins | 30 | 9.67e-02 | -1.75e-01 | 4.74e-01 |
EGFR downregulation | 31 | 9.16e-02 | -1.75e-01 | 4.63e-01 |
Signaling by EGFR in Cancer | 25 | 1.31e-01 | -1.75e-01 | 5.13e-01 |
Extra-nuclear estrogen signaling | 75 | 8.99e-03 | -1.74e-01 | 1.79e-01 |
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 60 | 1.96e-02 | -1.74e-01 | 2.51e-01 |
Leading Strand Synthesis | 14 | 2.59e-01 | 1.74e-01 | 6.53e-01 |
Polymerase switching | 14 | 2.59e-01 | 1.74e-01 | 6.53e-01 |
Dopamine Neurotransmitter Release Cycle | 23 | 1.49e-01 | 1.74e-01 | 5.49e-01 |
ABC transporter disorders | 78 | 7.91e-03 | 1.74e-01 | 1.67e-01 |
Metabolism of Angiotensinogen to Angiotensins | 18 | 2.03e-01 | 1.73e-01 | 6.08e-01 |
Cross-presentation of particulate exogenous antigens (phagosomes) | 8 | 3.96e-01 | -1.73e-01 | 7.55e-01 |
RUNX1 regulates transcription of genes involved in interleukin signaling | 5 | 5.03e-01 | 1.73e-01 | 8.13e-01 |
mitochondrial fatty acid beta-oxidation of unsaturated fatty acids | 6 | 4.63e-01 | 1.73e-01 | 7.94e-01 |
Reversal of alkylation damage by DNA dioxygenases | 7 | 4.29e-01 | -1.73e-01 | 7.75e-01 |
Endosomal/Vacuolar pathway | 12 | 3.01e-01 | -1.72e-01 | 6.87e-01 |
Calcitonin-like ligand receptors | 10 | 3.46e-01 | 1.72e-01 | 7.15e-01 |
BBSome-mediated cargo-targeting to cilium | 23 | 1.53e-01 | 1.72e-01 | 5.54e-01 |
NFE2L2 regulates pentose phosphate pathway genes | 8 | 4.01e-01 | -1.71e-01 | 7.62e-01 |
Apoptotic factor-mediated response | 19 | 1.96e-01 | -1.71e-01 | 6.07e-01 |
SHC1 events in ERBB2 signaling | 22 | 1.65e-01 | -1.71e-01 | 5.78e-01 |
RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | 10 | 3.49e-01 | 1.71e-01 | 7.17e-01 |
Josephin domain DUBs | 11 | 3.26e-01 | 1.71e-01 | 7.07e-01 |
Regulation of RUNX3 expression and activity | 55 | 2.85e-02 | 1.71e-01 | 2.93e-01 |
Formation of the beta-catenin:TCF transactivating complex | 55 | 2.86e-02 | -1.71e-01 | 2.93e-01 |
NFE2L2 regulating ER-stress associated genes | 5 | 5.09e-01 | -1.70e-01 | 8.13e-01 |
Prostacyclin signalling through prostacyclin receptor | 19 | 1.99e-01 | -1.70e-01 | 6.07e-01 |
GPER1 signaling | 45 | 4.83e-02 | -1.70e-01 | 3.69e-01 |
Interleukin receptor SHC signaling | 24 | 1.49e-01 | -1.70e-01 | 5.50e-01 |
Regulation of RUNX2 expression and activity | 73 | 1.23e-02 | 1.69e-01 | 2.06e-01 |
FCERI mediated Ca+2 mobilization | 31 | 1.03e-01 | 1.69e-01 | 4.85e-01 |
Sulfur amino acid metabolism | 27 | 1.29e-01 | -1.69e-01 | 5.13e-01 |
Interconversion of nucleotide di- and triphosphates | 30 | 1.10e-01 | -1.69e-01 | 4.93e-01 |
Activated NTRK2 signals through CDK5 | 6 | 4.75e-01 | 1.68e-01 | 7.99e-01 |
PKMTs methylate histone lysines | 44 | 5.36e-02 | -1.68e-01 | 3.87e-01 |
DARPP-32 events | 24 | 1.54e-01 | -1.68e-01 | 5.54e-01 |
LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production | 5 | 5.16e-01 | -1.68e-01 | 8.15e-01 |
RMTs methylate histone arginines | 44 | 5.44e-02 | -1.68e-01 | 3.87e-01 |
p130Cas linkage to MAPK signaling for integrins | 15 | 2.62e-01 | -1.67e-01 | 6.57e-01 |
Signaling by Activin | 17 | 2.33e-01 | -1.67e-01 | 6.31e-01 |
Voltage gated Potassium channels | 43 | 5.82e-02 | 1.67e-01 | 3.90e-01 |
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 20 | 1.97e-01 | -1.67e-01 | 6.07e-01 |
Synthesis of DNA | 121 | 1.54e-03 | 1.67e-01 | 8.01e-02 |
G1/S-Specific Transcription | 29 | 1.22e-01 | 1.66e-01 | 5.02e-01 |
Phase 4 - resting membrane potential | 19 | 2.11e-01 | 1.66e-01 | 6.17e-01 |
RET signaling | 41 | 6.66e-02 | -1.66e-01 | 4.06e-01 |
Signaling by VEGF | 106 | 3.27e-03 | -1.65e-01 | 1.01e-01 |
Beta oxidation of butanoyl-CoA to acetyl-CoA | 5 | 5.23e-01 | -1.65e-01 | 8.18e-01 |
RHOC GTPase cycle | 72 | 1.60e-02 | -1.64e-01 | 2.31e-01 |
VLDL clearance | 6 | 4.86e-01 | -1.64e-01 | 8.03e-01 |
CDC42 GTPase cycle | 153 | 4.60e-04 | -1.64e-01 | 4.02e-02 |
Vasopressin regulates renal water homeostasis via Aquaporins | 43 | 6.28e-02 | -1.64e-01 | 3.97e-01 |
Signal transduction by L1 | 21 | 1.94e-01 | -1.64e-01 | 6.07e-01 |
Constitutive Signaling by EGFRvIII | 15 | 2.72e-01 | -1.64e-01 | 6.68e-01 |
Signaling by EGFRvIII in Cancer | 15 | 2.72e-01 | -1.64e-01 | 6.68e-01 |
Beta-catenin phosphorylation cascade | 17 | 2.42e-01 | -1.64e-01 | 6.40e-01 |
Mineralocorticoid biosynthesis | 6 | 4.87e-01 | 1.64e-01 | 8.04e-01 |
PINK1-PRKN Mediated Mitophagy | 21 | 1.95e-01 | 1.64e-01 | 6.07e-01 |
Wax and plasmalogen biosynthesis | 7 | 4.54e-01 | 1.63e-01 | 7.88e-01 |
Trafficking of myristoylated proteins to the cilium | 5 | 5.29e-01 | 1.63e-01 | 8.20e-01 |
Signaling by Leptin | 11 | 3.50e-01 | -1.63e-01 | 7.17e-01 |
Plasma lipoprotein assembly, remodeling, and clearance | 75 | 1.49e-02 | -1.63e-01 | 2.23e-01 |
Acetylcholine binding and downstream events | 14 | 2.92e-01 | 1.63e-01 | 6.82e-01 |
Postsynaptic nicotinic acetylcholine receptors | 14 | 2.92e-01 | 1.63e-01 | 6.82e-01 |
Nef mediated downregulation of MHC class I complex cell surface expression | 10 | 3.73e-01 | -1.63e-01 | 7.44e-01 |
Thromboxane signalling through TP receptor | 24 | 1.68e-01 | -1.62e-01 | 5.84e-01 |
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 55 | 3.73e-02 | 1.62e-01 | 3.36e-01 |
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 37 | 8.76e-02 | -1.62e-01 | 4.51e-01 |
Degradation of GLI1 by the proteasome | 60 | 2.97e-02 | 1.62e-01 | 2.97e-01 |
G alpha (12/13) signalling events | 79 | 1.29e-02 | -1.62e-01 | 2.09e-01 |
ERBB2 Regulates Cell Motility | 15 | 2.81e-01 | -1.61e-01 | 6.74e-01 |
Signaling by NOTCH3 | 49 | 5.15e-02 | -1.61e-01 | 3.79e-01 |
FGFR1b ligand binding and activation | 8 | 4.32e-01 | -1.60e-01 | 7.77e-01 |
Mitotic Telophase/Cytokinesis | 13 | 3.17e-01 | 1.60e-01 | 7.03e-01 |
Assembly of active LPL and LIPC lipase complexes | 19 | 2.27e-01 | -1.60e-01 | 6.26e-01 |
Synthesis of bile acids and bile salts via 27-hydroxycholesterol | 15 | 2.83e-01 | 1.60e-01 | 6.76e-01 |
RUNX3 Regulates Immune Response and Cell Migration | 6 | 4.97e-01 | 1.60e-01 | 8.12e-01 |
Glycerophospholipid biosynthesis | 126 | 1.95e-03 | -1.60e-01 | 9.51e-02 |
Caspase activation via extrinsic apoptotic signalling pathway | 26 | 1.59e-01 | -1.60e-01 | 5.63e-01 |
Activated NTRK3 signals through RAS | 8 | 4.35e-01 | 1.60e-01 | 7.77e-01 |
Inactivation of APC/C via direct inhibition of the APC/C complex | 21 | 2.07e-01 | 1.59e-01 | 6.09e-01 |
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 21 | 2.07e-01 | 1.59e-01 | 6.09e-01 |
Tryptophan catabolism | 14 | 3.03e-01 | -1.59e-01 | 6.89e-01 |
Signaling by PDGF | 58 | 3.64e-02 | -1.59e-01 | 3.33e-01 |
PTK6 Regulates Proteins Involved in RNA Processing | 5 | 5.39e-01 | 1.59e-01 | 8.24e-01 |
Purine catabolism | 17 | 2.57e-01 | -1.59e-01 | 6.51e-01 |
RAF-independent MAPK1/3 activation | 23 | 1.88e-01 | -1.59e-01 | 6.01e-01 |
Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | 58 | 3.70e-02 | -1.58e-01 | 3.35e-01 |
Interleukin-15 signaling | 14 | 3.06e-01 | -1.58e-01 | 6.93e-01 |
WNT5A-dependent internalization of FZD4 | 15 | 2.90e-01 | -1.58e-01 | 6.80e-01 |
Uptake and function of anthrax toxins | 11 | 3.65e-01 | -1.58e-01 | 7.37e-01 |
ADP signalling through P2Y purinoceptor 1 | 25 | 1.73e-01 | -1.58e-01 | 5.90e-01 |
Incretin synthesis, secretion, and inactivation | 24 | 1.82e-01 | 1.58e-01 | 5.96e-01 |
FGFR2 alternative splicing | 26 | 1.65e-01 | -1.57e-01 | 5.78e-01 |
Rab regulation of trafficking | 121 | 2.85e-03 | -1.57e-01 | 9.74e-02 |
Organic cation/anion/zwitterion transport | 15 | 2.93e-01 | -1.57e-01 | 6.82e-01 |
Erythropoietin activates Phospholipase C gamma (PLCG) | 7 | 4.73e-01 | -1.57e-01 | 7.97e-01 |
Ethanol oxidation | 12 | 3.48e-01 | 1.57e-01 | 7.17e-01 |
Organic anion transporters | 10 | 3.93e-01 | -1.56e-01 | 7.54e-01 |
Signalling to RAS | 20 | 2.28e-01 | -1.56e-01 | 6.26e-01 |
Insulin processing | 25 | 1.78e-01 | 1.56e-01 | 5.92e-01 |
Laminin interactions | 30 | 1.40e-01 | -1.56e-01 | 5.33e-01 |
Cohesin Loading onto Chromatin | 10 | 3.94e-01 | 1.56e-01 | 7.54e-01 |
Neurotransmitter release cycle | 51 | 5.48e-02 | 1.55e-01 | 3.87e-01 |
MET promotes cell motility | 41 | 8.51e-02 | -1.55e-01 | 4.50e-01 |
Formation of WDR5-containing histone-modifying complexes | 41 | 8.53e-02 | -1.55e-01 | 4.50e-01 |
DCC mediated attractive signaling | 14 | 3.17e-01 | -1.55e-01 | 7.03e-01 |
Acrosome Reaction and Sperm:Oocyte Membrane Binding | 6 | 5.12e-01 | 1.54e-01 | 8.15e-01 |
Interleukin-6 signaling | 11 | 3.77e-01 | -1.54e-01 | 7.47e-01 |
The retinoid cycle in cones (daylight vision) | 6 | 5.15e-01 | -1.54e-01 | 8.15e-01 |
NOTCH3 Activation and Transmission of Signal to the Nucleus | 25 | 1.84e-01 | -1.53e-01 | 5.99e-01 |
Signaling by MET | 79 | 1.85e-02 | -1.53e-01 | 2.43e-01 |
FOXO-mediated transcription of cell cycle genes | 17 | 2.74e-01 | 1.53e-01 | 6.70e-01 |
Signaling by ERBB2 | 50 | 6.14e-02 | -1.53e-01 | 3.93e-01 |
Nitric oxide stimulates guanylate cyclase | 21 | 2.26e-01 | 1.53e-01 | 6.26e-01 |
Initial triggering of complement | 22 | 2.16e-01 | -1.52e-01 | 6.20e-01 |
Activated NTRK2 signals through PI3K | 7 | 4.86e-01 | 1.52e-01 | 8.03e-01 |
Hedgehog ligand biogenesis | 65 | 3.42e-02 | 1.52e-01 | 3.25e-01 |
MECP2 regulates neuronal receptors and channels | 18 | 2.65e-01 | 1.52e-01 | 6.62e-01 |
Ca-dependent events | 37 | 1.10e-01 | -1.52e-01 | 4.93e-01 |
Lipid particle organization | 6 | 5.21e-01 | 1.51e-01 | 8.18e-01 |
RND2 GTPase cycle | 42 | 9.03e-02 | -1.51e-01 | 4.60e-01 |
Digestion | 19 | 2.54e-01 | 1.51e-01 | 6.48e-01 |
DAG and IP3 signaling | 41 | 9.46e-02 | -1.51e-01 | 4.69e-01 |
GLI3 is processed to GLI3R by the proteasome | 60 | 4.34e-02 | 1.51e-01 | 3.65e-01 |
GABA synthesis, release, reuptake and degradation | 19 | 2.57e-01 | 1.50e-01 | 6.51e-01 |
Regulation of ornithine decarboxylase (ODC) | 51 | 6.34e-02 | 1.50e-01 | 3.97e-01 |
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 65 | 3.67e-02 | 1.50e-01 | 3.34e-01 |
Zinc influx into cells by the SLC39 gene family | 10 | 4.12e-01 | -1.50e-01 | 7.67e-01 |
Interleukin-18 signaling | 8 | 4.63e-01 | -1.50e-01 | 7.94e-01 |
Nuclear Events (kinase and transcription factor activation) | 61 | 4.31e-02 | 1.50e-01 | 3.65e-01 |
Cargo concentration in the ER | 33 | 1.37e-01 | -1.50e-01 | 5.25e-01 |
Downregulation of ERBB4 signaling | 9 | 4.37e-01 | 1.49e-01 | 7.77e-01 |
Synthesis of UDP-N-acetyl-glucosamine | 8 | 4.65e-01 | 1.49e-01 | 7.95e-01 |
Regulation of PTEN stability and activity | 69 | 3.22e-02 | 1.49e-01 | 3.16e-01 |
RHOF GTPase cycle | 42 | 9.48e-02 | -1.49e-01 | 4.69e-01 |
POLB-Dependent Long Patch Base Excision Repair | 8 | 4.66e-01 | 1.49e-01 | 7.95e-01 |
G0 and Early G1 | 27 | 1.81e-01 | 1.49e-01 | 5.96e-01 |
Signaling by ERBB2 KD Mutants | 25 | 1.99e-01 | -1.48e-01 | 6.07e-01 |
Activation of the AP-1 family of transcription factors | 10 | 4.17e-01 | 1.48e-01 | 7.68e-01 |
Cell-Cell communication | 153 | 1.55e-03 | -1.48e-01 | 8.01e-02 |
FLT3 Signaling | 38 | 1.14e-01 | -1.48e-01 | 4.97e-01 |
Gain-of-function MRAS complexes activate RAF signaling | 8 | 4.68e-01 | -1.48e-01 | 7.95e-01 |
SHOC2 M1731 mutant abolishes MRAS complex function | 8 | 4.68e-01 | -1.48e-01 | 7.95e-01 |
Signaling by MRAS-complex mutants | 8 | 4.68e-01 | -1.48e-01 | 7.95e-01 |
RNA Polymerase I Promoter Opening | 26 | 1.91e-01 | -1.48e-01 | 6.06e-01 |
RHOA GTPase cycle | 147 | 1.99e-03 | -1.48e-01 | 9.51e-02 |
RND1 GTPase cycle | 42 | 9.78e-02 | -1.48e-01 | 4.75e-01 |
Degradation of GLI2 by the proteasome | 60 | 4.84e-02 | 1.47e-01 | 3.69e-01 |
Collagen formation | 90 | 1.58e-02 | -1.47e-01 | 2.31e-01 |
G beta:gamma signalling through PI3Kgamma | 25 | 2.04e-01 | -1.47e-01 | 6.08e-01 |
E2F mediated regulation of DNA replication | 21 | 2.45e-01 | 1.46e-01 | 6.42e-01 |
NIK–>noncanonical NF-kB signaling | 59 | 5.21e-02 | 1.46e-01 | 3.80e-01 |
The canonical retinoid cycle in rods (twilight vision) | 23 | 2.25e-01 | -1.46e-01 | 6.26e-01 |
Condensation of Prophase Chromosomes | 37 | 1.25e-01 | -1.46e-01 | 5.12e-01 |
Signaling by BRAF and RAF1 fusions | 65 | 4.24e-02 | -1.46e-01 | 3.61e-01 |
Condensation of Prometaphase Chromosomes | 11 | 4.03e-01 | 1.46e-01 | 7.64e-01 |
Somitogenesis | 55 | 6.21e-02 | 1.45e-01 | 3.96e-01 |
RAB GEFs exchange GTP for GDP on RABs | 88 | 1.84e-02 | -1.45e-01 | 2.43e-01 |
Phase 0 - rapid depolarisation | 32 | 1.55e-01 | 1.45e-01 | 5.54e-01 |
Interleukin-2 signaling | 12 | 3.84e-01 | -1.45e-01 | 7.51e-01 |
ERKs are inactivated | 13 | 3.65e-01 | -1.45e-01 | 7.37e-01 |
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 42 | 1.04e-01 | -1.45e-01 | 4.86e-01 |
RHOBTB1 GTPase cycle | 23 | 2.32e-01 | 1.44e-01 | 6.31e-01 |
Activation of HOX genes during differentiation | 85 | 2.21e-02 | -1.44e-01 | 2.66e-01 |
Activation of anterior HOX genes in hindbrain development during early embryogenesis | 85 | 2.21e-02 | -1.44e-01 | 2.66e-01 |
Interaction between L1 and Ankyrins | 31 | 1.67e-01 | 1.44e-01 | 5.81e-01 |
Neurotoxicity of clostridium toxins | 10 | 4.32e-01 | 1.44e-01 | 7.77e-01 |
Ephrin signaling | 19 | 2.79e-01 | -1.43e-01 | 6.74e-01 |
Synaptic adhesion-like molecules | 21 | 2.56e-01 | -1.43e-01 | 6.51e-01 |
Scavenging by Class F Receptors | 6 | 5.44e-01 | 1.43e-01 | 8.30e-01 |
HDACs deacetylate histones | 58 | 5.94e-02 | -1.43e-01 | 3.90e-01 |
Downregulation of ERBB2:ERBB3 signaling | 13 | 3.73e-01 | -1.43e-01 | 7.44e-01 |
MAPK6/MAPK4 signaling | 92 | 1.81e-02 | 1.43e-01 | 2.41e-01 |
Signaling by FGFR1 in disease | 38 | 1.29e-01 | -1.42e-01 | 5.13e-01 |
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 58 | 6.05e-02 | -1.42e-01 | 3.90e-01 |
Constitutive Signaling by NOTCH1 PEST Domain Mutants | 58 | 6.05e-02 | -1.42e-01 | 3.90e-01 |
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 58 | 6.05e-02 | -1.42e-01 | 3.90e-01 |
Signaling by NOTCH1 PEST Domain Mutants in Cancer | 58 | 6.05e-02 | -1.42e-01 | 3.90e-01 |
Signaling by NOTCH1 in Cancer | 58 | 6.05e-02 | -1.42e-01 | 3.90e-01 |
ADORA2B mediated anti-inflammatory cytokines production | 43 | 1.06e-01 | -1.42e-01 | 4.89e-01 |
Collagen biosynthesis and modifying enzymes | 67 | 4.43e-02 | -1.42e-01 | 3.67e-01 |
Regulation of NF-kappa B signaling | 18 | 2.97e-01 | -1.42e-01 | 6.84e-01 |
FCERI mediated NF-kB activation | 81 | 2.72e-02 | 1.42e-01 | 2.90e-01 |
Response of EIF2AK1 (HRI) to heme deficiency | 15 | 3.41e-01 | 1.42e-01 | 7.12e-01 |
Proton-coupled monocarboxylate transport | 6 | 5.48e-01 | -1.42e-01 | 8.30e-01 |
CaM pathway | 35 | 1.48e-01 | -1.41e-01 | 5.46e-01 |
Calmodulin induced events | 35 | 1.48e-01 | -1.41e-01 | 5.46e-01 |
Transcriptional activation of mitochondrial biogenesis | 53 | 7.50e-02 | -1.41e-01 | 4.28e-01 |
Signaling by FLT3 ITD and TKD mutants | 16 | 3.28e-01 | -1.41e-01 | 7.07e-01 |
Digestion and absorption | 24 | 2.31e-01 | 1.41e-01 | 6.31e-01 |
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 27 | 2.04e-01 | 1.41e-01 | 6.08e-01 |
Regulated Necrosis | 58 | 6.35e-02 | -1.41e-01 | 3.97e-01 |
Dectin-1 mediated noncanonical NF-kB signaling | 62 | 5.62e-02 | 1.40e-01 | 3.90e-01 |
Activated NTRK2 signals through FYN | 7 | 5.21e-01 | 1.40e-01 | 8.18e-01 |
Heme signaling | 46 | 1.01e-01 | -1.40e-01 | 4.79e-01 |
Cyclin E associated events during G1/S transition | 83 | 2.77e-02 | 1.40e-01 | 2.90e-01 |
Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | 8 | 4.94e-01 | 1.40e-01 | 8.10e-01 |
MET activates PTK2 signaling | 30 | 1.86e-01 | -1.39e-01 | 6.01e-01 |
Digestion of dietary carbohydrate | 7 | 5.23e-01 | 1.39e-01 | 8.18e-01 |
Signaling by Hippo | 20 | 2.81e-01 | -1.39e-01 | 6.75e-01 |
Apoptotic cleavage of cellular proteins | 38 | 1.38e-01 | -1.39e-01 | 5.27e-01 |
Signaling by WNT in cancer | 34 | 1.61e-01 | -1.39e-01 | 5.67e-01 |
RAB geranylgeranylation | 64 | 5.47e-02 | -1.39e-01 | 3.87e-01 |
Signaling by FLT3 fusion proteins | 19 | 2.95e-01 | -1.39e-01 | 6.84e-01 |
G1/S Transition | 130 | 6.36e-03 | 1.39e-01 | 1.50e-01 |
Nonhomologous End-Joining (NHEJ) | 47 | 1.00e-01 | -1.39e-01 | 4.79e-01 |
Methionine salvage pathway | 6 | 5.57e-01 | -1.39e-01 | 8.33e-01 |
Methylation | 14 | 3.70e-01 | 1.38e-01 | 7.40e-01 |
Tachykinin receptors bind tachykinins | 5 | 5.92e-01 | 1.38e-01 | 8.56e-01 |
Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 10 | 4.49e-01 | -1.38e-01 | 7.86e-01 |
Phase I - Functionalization of compounds | 105 | 1.45e-02 | 1.38e-01 | 2.22e-01 |
Formation of tubulin folding intermediates by CCT/TriC | 25 | 2.33e-01 | 1.38e-01 | 6.31e-01 |
Assembly of collagen fibrils and other multimeric structures | 61 | 6.29e-02 | -1.38e-01 | 3.97e-01 |
RHO GTPases activate PKNs | 57 | 7.27e-02 | -1.37e-01 | 4.25e-01 |
Vitamin B1 (thiamin) metabolism | 5 | 5.96e-01 | 1.37e-01 | 8.57e-01 |
AKT phosphorylates targets in the cytosol | 14 | 3.76e-01 | -1.37e-01 | 7.47e-01 |
Translation of Replicase and Assembly of the Replication Transcription Complex 9679504 | 13 | 3.94e-01 | -1.37e-01 | 7.54e-01 |
Negative regulation of NOTCH4 signaling | 54 | 8.29e-02 | 1.36e-01 | 4.50e-01 |
RNA Polymerase I Transcription Termination | 29 | 2.05e-01 | 1.36e-01 | 6.08e-01 |
Regulation of MECP2 expression and activity | 32 | 1.83e-01 | -1.36e-01 | 5.98e-01 |
InlA-mediated entry of Listeria monocytogenes into host cells | 9 | 4.80e-01 | -1.36e-01 | 8.02e-01 |
Phospholipid metabolism | 208 | 7.31e-04 | -1.36e-01 | 5.45e-02 |
Regulation of TP53 Expression and Degradation | 37 | 1.54e-01 | -1.35e-01 | 5.54e-01 |
Class I peroxisomal membrane protein import | 20 | 2.95e-01 | 1.35e-01 | 6.84e-01 |
Interferon alpha/beta signaling | 72 | 4.72e-02 | -1.35e-01 | 3.68e-01 |
Regulation of gene expression by Hypoxia-inducible Factor | 10 | 4.59e-01 | -1.35e-01 | 7.92e-01 |
Signaling by ERBB2 TMD/JMD mutants | 22 | 2.73e-01 | -1.35e-01 | 6.69e-01 |
Formation of ATP by chemiosmotic coupling | 16 | 3.50e-01 | 1.35e-01 | 7.17e-01 |
Unwinding of DNA | 12 | 4.18e-01 | 1.35e-01 | 7.69e-01 |
RUNX3 regulates CDKN1A transcription | 7 | 5.38e-01 | -1.34e-01 | 8.24e-01 |
SHC-related events triggered by IGF1R | 9 | 4.85e-01 | -1.34e-01 | 8.03e-01 |
EPH-ephrin mediated repulsion of cells | 51 | 9.70e-02 | -1.34e-01 | 4.74e-01 |
TRAF6 mediated NF-kB activation | 25 | 2.46e-01 | -1.34e-01 | 6.42e-01 |
UCH proteinases | 96 | 2.32e-02 | 1.34e-01 | 2.73e-01 |
COPII-mediated vesicle transport | 68 | 5.61e-02 | -1.34e-01 | 3.90e-01 |
S Phase | 163 | 3.19e-03 | 1.34e-01 | 1.00e-01 |
PI3K events in ERBB4 signaling | 10 | 4.65e-01 | -1.33e-01 | 7.95e-01 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 18 | 3.27e-01 | -1.33e-01 | 7.07e-01 |
Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 30 | 2.06e-01 | -1.33e-01 | 6.09e-01 |
Beta oxidation of hexanoyl-CoA to butanoyl-CoA | 5 | 6.06e-01 | -1.33e-01 | 8.62e-01 |
Golgi Cisternae Pericentriolar Stack Reorganization | 14 | 3.89e-01 | 1.33e-01 | 7.52e-01 |
p75 NTR receptor-mediated signalling | 97 | 2.36e-02 | -1.33e-01 | 2.76e-01 |
Regulation of RAS by GAPs | 67 | 5.99e-02 | 1.33e-01 | 3.90e-01 |
PLC beta mediated events | 49 | 1.09e-01 | -1.32e-01 | 4.92e-01 |
Chromatin modifying enzymes | 229 | 5.93e-04 | -1.32e-01 | 4.77e-02 |
Chromatin organization | 229 | 5.93e-04 | -1.32e-01 | 4.77e-02 |
Beta-oxidation of pristanoyl-CoA | 9 | 4.94e-01 | -1.32e-01 | 8.10e-01 |
Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 41 | 1.45e-01 | 1.32e-01 | 5.42e-01 |
Diseases of DNA Double-Strand Break Repair | 41 | 1.45e-01 | 1.32e-01 | 5.42e-01 |
Cell-cell junction organization | 90 | 3.27e-02 | -1.30e-01 | 3.18e-01 |
NOTCH4 Activation and Transmission of Signal to the Nucleus | 11 | 4.55e-01 | -1.30e-01 | 7.88e-01 |
Cell death signalling via NRAGE, NRIF and NADE | 75 | 5.13e-02 | -1.30e-01 | 3.79e-01 |
Activation of IRF3, IRF7 mediated by TBK1, IKBKE | 17 | 3.53e-01 | -1.30e-01 | 7.19e-01 |
Inflammasomes | 21 | 3.02e-01 | -1.30e-01 | 6.89e-01 |
G-protein activation | 24 | 2.72e-01 | -1.30e-01 | 6.68e-01 |
Heparan sulfate/heparin (HS-GAG) metabolism | 57 | 9.18e-02 | -1.29e-01 | 4.63e-01 |
Prevention of phagosomal-lysosomal fusion | 9 | 5.03e-01 | 1.29e-01 | 8.13e-01 |
Germ layer formation at gastrulation | 16 | 3.72e-01 | 1.29e-01 | 7.42e-01 |
Detoxification of Reactive Oxygen Species | 36 | 1.82e-01 | -1.29e-01 | 5.96e-01 |
Regulation of lipid metabolism by PPARalpha | 118 | 1.58e-02 | -1.29e-01 | 2.31e-01 |
Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | 10 | 4.81e-01 | 1.29e-01 | 8.03e-01 |
Zygotic genome activation (ZGA) | 13 | 4.22e-01 | 1.29e-01 | 7.69e-01 |
PPARA activates gene expression | 116 | 1.69e-02 | -1.28e-01 | 2.36e-01 |
Aquaporin-mediated transport | 52 | 1.09e-01 | -1.28e-01 | 4.93e-01 |
Gluconeogenesis | 35 | 1.91e-01 | -1.28e-01 | 6.05e-01 |
RAC1 GTPase cycle | 183 | 2.88e-03 | -1.28e-01 | 9.74e-02 |
PKA-mediated phosphorylation of CREB | 20 | 3.23e-01 | -1.28e-01 | 7.07e-01 |
Keratinization | 207 | 1.55e-03 | 1.28e-01 | 8.01e-02 |
Regulation of PTEN localization | 9 | 5.08e-01 | 1.28e-01 | 8.13e-01 |
Hyaluronan biosynthesis and export | 5 | 6.22e-01 | -1.27e-01 | 8.63e-01 |
YAP1- and WWTR1 (TAZ)-stimulated gene expression | 14 | 4.09e-01 | -1.27e-01 | 7.67e-01 |
TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | 5 | 6.22e-01 | -1.27e-01 | 8.63e-01 |
TRAIL signaling | 8 | 5.33e-01 | -1.27e-01 | 8.21e-01 |
Nuclear signaling by ERBB4 | 32 | 2.12e-01 | -1.27e-01 | 6.18e-01 |
Synthesis of very long-chain fatty acyl-CoAs | 24 | 2.80e-01 | 1.27e-01 | 6.74e-01 |
The role of GTSE1 in G2/M progression after G2 checkpoint | 77 | 5.44e-02 | 1.27e-01 | 3.87e-01 |
Diseases of DNA repair | 51 | 1.17e-01 | 1.27e-01 | 5.00e-01 |
The NLRP3 inflammasome | 16 | 3.80e-01 | -1.27e-01 | 7.48e-01 |
Signaling by Nuclear Receptors | 267 | 3.75e-04 | -1.26e-01 | 3.42e-02 |
Peptide hormone metabolism | 86 | 4.27e-02 | 1.26e-01 | 3.63e-01 |
Unblocking of NMDA receptors, glutamate binding and activation | 21 | 3.16e-01 | 1.26e-01 | 7.03e-01 |
ABC-family proteins mediated transport | 103 | 2.74e-02 | 1.26e-01 | 2.90e-01 |
Basigin interactions | 25 | 2.77e-01 | -1.26e-01 | 6.73e-01 |
Signaling by SCF-KIT | 43 | 1.55e-01 | -1.25e-01 | 5.54e-01 |
Activation of NF-kappaB in B cells | 67 | 7.62e-02 | 1.25e-01 | 4.31e-01 |
NCAM signaling for neurite out-growth | 63 | 8.57e-02 | -1.25e-01 | 4.50e-01 |
Purine ribonucleoside monophosphate biosynthesis | 9 | 5.16e-01 | 1.25e-01 | 8.15e-01 |
Heme biosynthesis | 14 | 4.18e-01 | 1.25e-01 | 7.69e-01 |
Presynaptic phase of homologous DNA pairing and strand exchange | 40 | 1.72e-01 | 1.25e-01 | 5.89e-01 |
Acetylcholine regulates insulin secretion | 10 | 4.94e-01 | -1.25e-01 | 8.10e-01 |
mRNA Capping | 28 | 2.54e-01 | 1.25e-01 | 6.48e-01 |
RUNX3 regulates NOTCH signaling | 14 | 4.22e-01 | -1.24e-01 | 7.69e-01 |
Chondroitin sulfate/dermatan sulfate metabolism | 50 | 1.30e-01 | -1.24e-01 | 5.13e-01 |
Erythrocytes take up carbon dioxide and release oxygen | 12 | 4.58e-01 | -1.24e-01 | 7.92e-01 |
O2/CO2 exchange in erythrocytes | 12 | 4.58e-01 | -1.24e-01 | 7.92e-01 |
G-protein mediated events | 54 | 1.16e-01 | -1.23e-01 | 5.00e-01 |
Translation of Replicase and Assembly of the Replication Transcription Complex 9694676 | 14 | 4.24e-01 | -1.23e-01 | 7.69e-01 |
Synthesis of PE | 13 | 4.42e-01 | -1.23e-01 | 7.80e-01 |
FGFR1 mutant receptor activation | 31 | 2.35e-01 | -1.23e-01 | 6.34e-01 |
RAC2 GTPase cycle | 88 | 4.58e-02 | -1.23e-01 | 3.67e-01 |
Regulation of innate immune responses to cytosolic DNA | 15 | 4.09e-01 | 1.23e-01 | 7.67e-01 |
Signaling by FGFR3 | 40 | 1.79e-01 | -1.23e-01 | 5.94e-01 |
SUMOylation of transcription factors | 20 | 3.42e-01 | 1.23e-01 | 7.12e-01 |
Integration of energy metabolism | 107 | 2.88e-02 | -1.22e-01 | 2.93e-01 |
RHOQ GTPase cycle | 59 | 1.05e-01 | -1.22e-01 | 4.87e-01 |
Toxicity of botulinum toxin type D (botD) | 5 | 6.36e-01 | 1.22e-01 | 8.72e-01 |
Toxicity of botulinum toxin type F (botF) | 5 | 6.36e-01 | 1.22e-01 | 8.72e-01 |
Metabolism of carbohydrates | 298 | 2.87e-04 | -1.22e-01 | 2.88e-02 |
PCNA-Dependent Long Patch Base Excision Repair | 21 | 3.33e-01 | 1.22e-01 | 7.12e-01 |
Cyclin A:Cdk2-associated events at S phase entry | 85 | 5.22e-02 | 1.22e-01 | 3.80e-01 |
TRAF3-dependent IRF activation pathway | 15 | 4.15e-01 | -1.22e-01 | 7.67e-01 |
Unfolded Protein Response (UPR) | 89 | 4.75e-02 | -1.21e-01 | 3.68e-01 |
RNA Pol II CTD phosphorylation and interaction with CE | 26 | 2.84e-01 | 1.21e-01 | 6.76e-01 |
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 26 | 2.84e-01 | 1.21e-01 | 6.76e-01 |
ESR-mediated signaling | 187 | 4.20e-03 | -1.21e-01 | 1.15e-01 |
Signaling by membrane-tethered fusions of PDGFRA or PDGFRB | 5 | 6.39e-01 | -1.21e-01 | 8.74e-01 |
Response of EIF2AK4 (GCN2) to amino acid deficiency | 101 | 3.54e-02 | 1.21e-01 | 3.27e-01 |
Abacavir ADME | 9 | 5.30e-01 | 1.21e-01 | 8.21e-01 |
Glycosphingolipid metabolism | 58 | 1.11e-01 | -1.21e-01 | 4.95e-01 |
Impaired BRCA2 binding to RAD51 | 35 | 2.17e-01 | 1.21e-01 | 6.22e-01 |
Mitotic G1 phase and G1/S transition | 148 | 1.14e-02 | 1.21e-01 | 1.97e-01 |
DNA Replication | 151 | 1.09e-02 | 1.20e-01 | 1.95e-01 |
Signaling by MAPK mutants | 7 | 5.83e-01 | 1.20e-01 | 8.49e-01 |
Removal of the Flap Intermediate from the C-strand | 17 | 3.93e-01 | 1.20e-01 | 7.54e-01 |
KSRP (KHSRP) binds and destabilizes mRNA | 17 | 3.94e-01 | -1.20e-01 | 7.54e-01 |
MET Receptor Activation | 6 | 6.12e-01 | -1.19e-01 | 8.63e-01 |
DNA Replication Pre-Initiation | 123 | 2.27e-02 | 1.19e-01 | 2.68e-01 |
G2/M Checkpoints | 146 | 1.33e-02 | 1.19e-01 | 2.13e-01 |
Activated NTRK3 signals through PI3K | 6 | 6.16e-01 | -1.18e-01 | 8.63e-01 |
Glucose metabolism | 94 | 4.75e-02 | -1.18e-01 | 3.68e-01 |
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 14 | 4.45e-01 | 1.18e-01 | 7.83e-01 |
Pexophagy | 10 | 5.19e-01 | 1.18e-01 | 8.18e-01 |
Metabolism of nucleotides | 96 | 4.62e-02 | -1.18e-01 | 3.67e-01 |
Mitochondrial iron-sulfur cluster biogenesis | 13 | 4.63e-01 | 1.18e-01 | 7.94e-01 |
Assembly and cell surface presentation of NMDA receptors | 42 | 1.87e-01 | 1.18e-01 | 6.01e-01 |
Signaling by ERBB2 in Cancer | 26 | 3.00e-01 | -1.17e-01 | 6.86e-01 |
Muscarinic acetylcholine receptors | 5 | 6.49e-01 | -1.17e-01 | 8.75e-01 |
Opioid Signalling | 90 | 5.45e-02 | -1.17e-01 | 3.87e-01 |
TAK1-dependent IKK and NF-kappa-B activation | 44 | 1.79e-01 | -1.17e-01 | 5.94e-01 |
FCGR3A-mediated phagocytosis | 59 | 1.20e-01 | -1.17e-01 | 5.00e-01 |
Leishmania phagocytosis | 59 | 1.20e-01 | -1.17e-01 | 5.00e-01 |
Parasite infection | 59 | 1.20e-01 | -1.17e-01 | 5.00e-01 |
Metabolism of polyamines | 59 | 1.20e-01 | 1.17e-01 | 5.00e-01 |
Downstream TCR signaling | 95 | 4.91e-02 | 1.17e-01 | 3.70e-01 |
Signaling by FGFR3 in disease | 22 | 3.43e-01 | -1.17e-01 | 7.12e-01 |
Transcriptional Regulation by VENTX | 41 | 1.97e-01 | -1.16e-01 | 6.07e-01 |
Processing and activation of SUMO | 10 | 5.24e-01 | 1.16e-01 | 8.18e-01 |
Regulation of TP53 Degradation | 36 | 2.27e-01 | -1.16e-01 | 6.26e-01 |
Hyaluronan metabolism | 17 | 4.07e-01 | -1.16e-01 | 7.67e-01 |
Diseases associated with glycosaminoglycan metabolism | 41 | 1.98e-01 | -1.16e-01 | 6.07e-01 |
Transcription of E2F targets under negative control by DREAM complex | 19 | 3.83e-01 | 1.16e-01 | 7.51e-01 |
SRP-dependent cotranslational protein targeting to membrane | 112 | 3.51e-02 | 1.15e-01 | 3.27e-01 |
Aflatoxin activation and detoxification | 19 | 3.84e-01 | -1.15e-01 | 7.51e-01 |
Activation of NOXA and translocation to mitochondria | 5 | 6.56e-01 | -1.15e-01 | 8.76e-01 |
GLI proteins bind promoters of Hh responsive genes to promote transcription | 7 | 5.99e-01 | -1.15e-01 | 8.57e-01 |
Apoptotic execution phase | 52 | 1.53e-01 | -1.15e-01 | 5.54e-01 |
RND3 GTPase cycle | 42 | 1.99e-01 | -1.14e-01 | 6.07e-01 |
MyD88 dependent cascade initiated on endosome | 102 | 4.62e-02 | -1.14e-01 | 3.67e-01 |
Keratan sulfate degradation | 15 | 4.44e-01 | -1.14e-01 | 7.82e-01 |
N-glycan trimming and elongation in the cis-Golgi | 5 | 6.59e-01 | 1.14e-01 | 8.78e-01 |
Specification of primordial germ cells | 11 | 5.13e-01 | -1.14e-01 | 8.15e-01 |
Polymerase switching on the C-strand of the telomere | 26 | 3.14e-01 | 1.14e-01 | 7.03e-01 |
Butyrophilin (BTN) family interactions | 12 | 4.94e-01 | -1.14e-01 | 8.10e-01 |
Viral mRNA Translation | 89 | 6.34e-02 | 1.14e-01 | 3.97e-01 |
Homologous DNA Pairing and Strand Exchange | 43 | 1.97e-01 | 1.14e-01 | 6.07e-01 |
Glycosaminoglycan metabolism | 126 | 2.75e-02 | -1.14e-01 | 2.90e-01 |
Removal of the Flap Intermediate | 14 | 4.61e-01 | 1.14e-01 | 7.94e-01 |
CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde | 8 | 5.79e-01 | -1.13e-01 | 8.48e-01 |
Regulation of FZD by ubiquitination | 21 | 3.68e-01 | 1.13e-01 | 7.39e-01 |
Signaling by ALK fusions and activated point mutants | 93 | 5.88e-02 | -1.13e-01 | 3.90e-01 |
Signaling by ALK in cancer | 93 | 5.88e-02 | -1.13e-01 | 3.90e-01 |
RHO GTPase cycle | 444 | 4.22e-05 | -1.13e-01 | 6.06e-03 |
SARS-CoV-1 modulates host translation machinery | 36 | 2.41e-01 | 1.13e-01 | 6.40e-01 |
Signaling by PDGFRA extracellular domain mutants | 12 | 4.99e-01 | -1.13e-01 | 8.12e-01 |
Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 12 | 4.99e-01 | -1.13e-01 | 8.12e-01 |
TFAP2 (AP-2) family regulates transcription of cell cycle factors | 5 | 6.63e-01 | -1.13e-01 | 8.80e-01 |
Regulation of TP53 Activity through Phosphorylation | 92 | 6.23e-02 | 1.12e-01 | 3.96e-01 |
Phenylalanine metabolism | 6 | 6.34e-01 | -1.12e-01 | 8.71e-01 |
Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 17 | 4.23e-01 | -1.12e-01 | 7.69e-01 |
Defects in biotin (Btn) metabolism | 8 | 5.83e-01 | -1.12e-01 | 8.49e-01 |
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 20 | 3.86e-01 | 1.12e-01 | 7.51e-01 |
Formation of paraxial mesoderm | 69 | 1.09e-01 | 1.12e-01 | 4.92e-01 |
PRC2 methylates histones and DNA | 36 | 2.46e-01 | -1.12e-01 | 6.42e-01 |
Signaling by FGFR | 89 | 6.87e-02 | -1.12e-01 | 4.08e-01 |
Hyaluronan uptake and degradation | 12 | 5.03e-01 | -1.12e-01 | 8.13e-01 |
mRNA decay by 3’ to 5’ exoribonuclease | 16 | 4.40e-01 | -1.12e-01 | 7.80e-01 |
Regulation of NPAS4 gene expression | 13 | 4.86e-01 | -1.12e-01 | 8.03e-01 |
DNA strand elongation | 32 | 2.75e-01 | 1.12e-01 | 6.71e-01 |
Cation-coupled Chloride cotransporters | 7 | 6.10e-01 | 1.11e-01 | 8.63e-01 |
Budding and maturation of HIV virion | 28 | 3.10e-01 | -1.11e-01 | 6.97e-01 |
Endosomal Sorting Complex Required For Transport (ESCRT) | 31 | 2.87e-01 | -1.11e-01 | 6.77e-01 |
Downstream signaling events of B Cell Receptor (BCR) | 81 | 8.60e-02 | 1.10e-01 | 4.50e-01 |
Regulation of expression of SLITs and ROBOs | 171 | 1.29e-02 | 1.10e-01 | 2.09e-01 |
Negative regulation of the PI3K/AKT network | 113 | 4.38e-02 | -1.10e-01 | 3.67e-01 |
TNFs bind their physiological receptors | 27 | 3.26e-01 | -1.09e-01 | 7.07e-01 |
Regulation of FOXO transcriptional activity by acetylation | 10 | 5.50e-01 | -1.09e-01 | 8.30e-01 |
Cholesterol biosynthesis | 27 | 3.27e-01 | -1.09e-01 | 7.07e-01 |
Translocation of ZAP-70 to Immunological synapse | 17 | 4.37e-01 | 1.09e-01 | 7.77e-01 |
p75NTR negatively regulates cell cycle via SC1 | 6 | 6.44e-01 | -1.09e-01 | 8.75e-01 |
Long-term potentiation | 23 | 3.67e-01 | 1.09e-01 | 7.39e-01 |
Signalling to p38 via RIT and RIN | 5 | 6.74e-01 | 1.09e-01 | 8.86e-01 |
Sema3A PAK dependent Axon repulsion | 16 | 4.54e-01 | -1.08e-01 | 7.88e-01 |
Metalloprotease DUBs | 28 | 3.22e-01 | 1.08e-01 | 7.06e-01 |
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 38 | 2.50e-01 | 1.08e-01 | 6.47e-01 |
Regulation of TLR by endogenous ligand | 21 | 3.92e-01 | 1.08e-01 | 7.54e-01 |
Fatty Acids bound to GPR40 (FFAR1) regulate insulin secretion | 8 | 5.97e-01 | -1.08e-01 | 8.57e-01 |
Toll Like Receptor 7/8 (TLR7/8) Cascade | 103 | 5.88e-02 | -1.08e-01 | 3.90e-01 |
Keratan sulfate/keratin metabolism | 36 | 2.63e-01 | -1.08e-01 | 6.59e-01 |
Packaging Of Telomere Ends | 29 | 3.18e-01 | -1.07e-01 | 7.03e-01 |
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 101 | 6.28e-02 | -1.07e-01 | 3.97e-01 |
Toll Like Receptor 9 (TLR9) Cascade | 106 | 5.66e-02 | -1.07e-01 | 3.90e-01 |
Fcgamma receptor (FCGR) dependent phagocytosis | 86 | 8.59e-02 | -1.07e-01 | 4.50e-01 |
rRNA modification in the nucleus and cytosol | 59 | 1.56e-01 | 1.07e-01 | 5.55e-01 |
NADE modulates death signalling | 6 | 6.50e-01 | -1.07e-01 | 8.75e-01 |
Response to metal ions | 14 | 4.89e-01 | -1.07e-01 | 8.04e-01 |
G alpha (z) signalling events | 48 | 2.02e-01 | -1.06e-01 | 6.08e-01 |
HDR through Single Strand Annealing (SSA) | 37 | 2.65e-01 | 1.06e-01 | 6.62e-01 |
Formation of definitive endoderm | 16 | 4.63e-01 | -1.06e-01 | 7.94e-01 |
Acyl chain remodelling of PS | 22 | 3.90e-01 | -1.06e-01 | 7.53e-01 |
Paradoxical activation of RAF signaling by kinase inactive BRAF | 44 | 2.25e-01 | -1.06e-01 | 6.26e-01 |
Signaling by RAS mutants | 44 | 2.25e-01 | -1.06e-01 | 6.26e-01 |
Signaling by moderate kinase activity BRAF mutants | 44 | 2.25e-01 | -1.06e-01 | 6.26e-01 |
Signaling downstream of RAS mutants | 44 | 2.25e-01 | -1.06e-01 | 6.26e-01 |
Assembly of the pre-replicative complex | 106 | 5.98e-02 | 1.06e-01 | 3.90e-01 |
Inactivation, recovery and regulation of the phototransduction cascade | 33 | 2.94e-01 | -1.06e-01 | 6.83e-01 |
Synthesis of PC | 28 | 3.33e-01 | -1.06e-01 | 7.12e-01 |
Synthesis of PIPs at the Golgi membrane | 18 | 4.38e-01 | 1.06e-01 | 7.77e-01 |
Regulation of NPAS4 mRNA translation | 9 | 5.84e-01 | -1.05e-01 | 8.49e-01 |
Phase 3 - rapid repolarisation | 9 | 5.84e-01 | -1.05e-01 | 8.49e-01 |
Nucleotide catabolism | 35 | 2.81e-01 | -1.05e-01 | 6.74e-01 |
Defects in cobalamin (B12) metabolism | 13 | 5.12e-01 | 1.05e-01 | 8.15e-01 |
PIWI-interacting RNA (piRNA) biogenesis | 29 | 3.27e-01 | 1.05e-01 | 7.07e-01 |
RUNX2 regulates chondrocyte maturation | 5 | 6.84e-01 | 1.05e-01 | 8.86e-01 |
Transport of vitamins, nucleosides, and related molecules | 42 | 2.40e-01 | -1.05e-01 | 6.39e-01 |
Regulation of CDH11 function | 11 | 5.47e-01 | -1.05e-01 | 8.30e-01 |
Acyl chain remodelling of PG | 18 | 4.42e-01 | -1.05e-01 | 7.80e-01 |
EPH-Ephrin signaling | 92 | 8.31e-02 | -1.05e-01 | 4.50e-01 |
Signaling by CSF3 (G-CSF) | 30 | 3.22e-01 | 1.05e-01 | 7.06e-01 |
Highly sodium permeable postsynaptic acetylcholine nicotinic receptors | 7 | 6.32e-01 | -1.04e-01 | 8.69e-01 |
Glycogen breakdown (glycogenolysis) | 14 | 4.99e-01 | -1.04e-01 | 8.12e-01 |
Leishmania infection | 162 | 2.19e-02 | -1.04e-01 | 2.66e-01 |
Parasitic Infection Pathways | 162 | 2.19e-02 | -1.04e-01 | 2.66e-01 |
Phase 2 - plateau phase | 15 | 4.84e-01 | -1.04e-01 | 8.03e-01 |
Oncogenic MAPK signaling | 81 | 1.05e-01 | -1.04e-01 | 4.87e-01 |
Role of LAT2/NTAL/LAB on calcium mobilization | 16 | 4.71e-01 | 1.04e-01 | 7.95e-01 |
Transport of organic anions | 11 | 5.50e-01 | 1.04e-01 | 8.30e-01 |
Intestinal absorption | 5 | 6.87e-01 | 1.04e-01 | 8.87e-01 |
Peptide chain elongation | 89 | 9.07e-02 | 1.04e-01 | 4.60e-01 |
Signaling by RAF1 mutants | 41 | 2.51e-01 | -1.04e-01 | 6.47e-01 |
Plasma lipoprotein remodeling | 34 | 2.96e-01 | -1.04e-01 | 6.84e-01 |
GRB2:SOS provides linkage to MAPK signaling for Integrins | 15 | 4.87e-01 | -1.04e-01 | 8.04e-01 |
Signal amplification | 33 | 3.03e-01 | -1.04e-01 | 6.89e-01 |
FOXO-mediated transcription of cell death genes | 16 | 4.74e-01 | -1.03e-01 | 7.98e-01 |
HIV Transcription Initiation | 46 | 2.26e-01 | 1.03e-01 | 6.26e-01 |
RNA Polymerase II HIV Promoter Escape | 46 | 2.26e-01 | 1.03e-01 | 6.26e-01 |
RNA Polymerase II Promoter Escape | 46 | 2.26e-01 | 1.03e-01 | 6.26e-01 |
RNA Polymerase II Transcription Initiation | 46 | 2.26e-01 | 1.03e-01 | 6.26e-01 |
RNA Polymerase II Transcription Initiation And Promoter Clearance | 46 | 2.26e-01 | 1.03e-01 | 6.26e-01 |
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 46 | 2.26e-01 | 1.03e-01 | 6.26e-01 |
CaMK IV-mediated phosphorylation of CREB | 10 | 5.72e-01 | -1.03e-01 | 8.46e-01 |
Molecules associated with elastic fibres | 37 | 2.78e-01 | -1.03e-01 | 6.74e-01 |
Formation of intermediate mesoderm | 8 | 6.14e-01 | 1.03e-01 | 8.63e-01 |
Kidney development | 46 | 2.27e-01 | 1.03e-01 | 6.26e-01 |
Formation of Incision Complex in GG-NER | 42 | 2.48e-01 | 1.03e-01 | 6.46e-01 |
Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 30 | 3.29e-01 | 1.03e-01 | 7.09e-01 |
Signaling by high-kinase activity BRAF mutants | 36 | 2.86e-01 | -1.03e-01 | 6.77e-01 |
Visual phototransduction | 99 | 7.77e-02 | -1.03e-01 | 4.35e-01 |
Eukaryotic Translation Termination | 93 | 8.77e-02 | 1.02e-01 | 4.51e-01 |
Purine salvage | 13 | 5.23e-01 | 1.02e-01 | 8.18e-01 |
Intrinsic Pathway of Fibrin Clot Formation | 23 | 3.96e-01 | -1.02e-01 | 7.55e-01 |
Generation of second messenger molecules | 31 | 3.26e-01 | 1.02e-01 | 7.07e-01 |
Elastic fibre formation | 44 | 2.42e-01 | -1.02e-01 | 6.40e-01 |
Circadian Clock | 67 | 1.49e-01 | -1.02e-01 | 5.50e-01 |
Transcriptional regulation of testis differentiation | 12 | 5.41e-01 | -1.02e-01 | 8.27e-01 |
Pausing and recovery of Tat-mediated HIV elongation | 31 | 3.27e-01 | -1.02e-01 | 7.07e-01 |
Tat-mediated HIV elongation arrest and recovery | 31 | 3.27e-01 | -1.02e-01 | 7.07e-01 |
Adrenaline,noradrenaline inhibits insulin secretion | 28 | 3.52e-01 | -1.02e-01 | 7.18e-01 |
Separation of Sister Chromatids | 188 | 1.63e-02 | 1.02e-01 | 2.32e-01 |
Organic cation transport | 10 | 5.78e-01 | -1.02e-01 | 8.48e-01 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 115 | 6.03e-02 | 1.01e-01 | 3.90e-01 |
Defective CHST3 causes SEDCJD | 8 | 6.20e-01 | 1.01e-01 | 8.63e-01 |
Spry regulation of FGF signaling | 16 | 4.84e-01 | -1.01e-01 | 8.03e-01 |
Miro GTPase Cycle | 8 | 6.21e-01 | -1.01e-01 | 8.63e-01 |
Cellular response to hypoxia | 74 | 1.33e-01 | 1.01e-01 | 5.17e-01 |
Processing of SMDT1 | 14 | 5.14e-01 | -1.01e-01 | 8.15e-01 |
Constitutive Signaling by NOTCH1 HD Domain Mutants | 15 | 4.99e-01 | -1.01e-01 | 8.12e-01 |
Signaling by NOTCH1 HD Domain Mutants in Cancer | 15 | 4.99e-01 | -1.01e-01 | 8.12e-01 |
The phototransduction cascade | 34 | 3.10e-01 | -1.01e-01 | 6.97e-01 |
STING mediated induction of host immune responses | 16 | 4.86e-01 | -1.01e-01 | 8.03e-01 |
Attachment of GPI anchor to uPAR | 7 | 6.46e-01 | -1.00e-01 | 8.75e-01 |
mTORC1-mediated signalling | 24 | 3.96e-01 | 1.00e-01 | 7.55e-01 |
Peptide hormone biosynthesis | 11 | 5.65e-01 | 1.00e-01 | 8.41e-01 |
Potential therapeutics for SARS | 98 | 8.71e-02 | -1.00e-01 | 4.51e-01 |
RUNX1 regulates expression of components of tight junctions | 5 | 6.99e-01 | -1.00e-01 | 8.90e-01 |
Insulin receptor signalling cascade | 54 | 2.04e-01 | -9.99e-02 | 6.08e-01 |
HS-GAG biosynthesis | 31 | 3.36e-01 | -9.98e-02 | 7.12e-01 |
Inactivation of CSF3 (G-CSF) signaling | 25 | 3.88e-01 | 9.98e-02 | 7.51e-01 |
Abacavir transmembrane transport | 5 | 6.99e-01 | 9.97e-02 | 8.90e-01 |
Suppression of phagosomal maturation | 13 | 5.34e-01 | 9.96e-02 | 8.21e-01 |
Listeria monocytogenes entry into host cells | 20 | 4.42e-01 | -9.94e-02 | 7.80e-01 |
VEGFR2 mediated cell proliferation | 19 | 4.54e-01 | -9.93e-02 | 7.88e-01 |
Receptor Mediated Mitophagy | 11 | 5.69e-01 | -9.92e-02 | 8.44e-01 |
Prefoldin mediated transfer of substrate to CCT/TriC | 27 | 3.74e-01 | 9.88e-02 | 7.45e-01 |
Disassembly of the destruction complex and recruitment of AXIN to the membrane | 31 | 3.42e-01 | -9.87e-02 | 7.12e-01 |
PKA-mediated phosphorylation of key metabolic factors | 5 | 7.03e-01 | -9.84e-02 | 8.91e-01 |
Gastrin-CREB signalling pathway via PKC and MAPK | 18 | 4.70e-01 | -9.84e-02 | 7.95e-01 |
Eukaryotic Translation Elongation | 93 | 1.02e-01 | 9.82e-02 | 4.80e-01 |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 32 | 3.36e-01 | 9.82e-02 | 7.12e-01 |
Sphingolipid metabolism | 107 | 8.03e-02 | -9.79e-02 | 4.41e-01 |
A tetrasaccharide linker sequence is required for GAG synthesis | 26 | 3.88e-01 | -9.78e-02 | 7.51e-01 |
Downstream signaling of activated FGFR3 | 25 | 3.98e-01 | -9.77e-02 | 7.56e-01 |
Selenocysteine synthesis | 92 | 1.06e-01 | 9.75e-02 | 4.89e-01 |
Crosslinking of collagen fibrils | 18 | 4.74e-01 | -9.75e-02 | 7.98e-01 |
Lagging Strand Synthesis | 20 | 4.51e-01 | 9.73e-02 | 7.87e-01 |
Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 12 | 5.60e-01 | -9.72e-02 | 8.36e-01 |
Formation of a pool of free 40S subunits | 100 | 9.31e-02 | 9.72e-02 | 4.67e-01 |
IRS-mediated signalling | 48 | 2.45e-01 | -9.70e-02 | 6.42e-01 |
Aberrant regulation of mitotic exit in cancer due to RB1 defects | 20 | 4.54e-01 | 9.66e-02 | 7.88e-01 |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 36 | 3.16e-01 | 9.65e-02 | 7.03e-01 |
Prostanoid ligand receptors | 9 | 6.16e-01 | -9.64e-02 | 8.63e-01 |
PI Metabolism | 83 | 1.29e-01 | -9.64e-02 | 5.13e-01 |
Signaling by Rho GTPases | 659 | 2.43e-05 | -9.63e-02 | 4.88e-03 |
Interleukin-7 signaling | 22 | 4.34e-01 | -9.63e-02 | 7.77e-01 |
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 51 | 2.35e-01 | 9.60e-02 | 6.35e-01 |
Protein methylation | 15 | 5.20e-01 | 9.60e-02 | 8.18e-01 |
Elevation of cytosolic Ca2+ levels | 16 | 5.06e-01 | 9.59e-02 | 8.13e-01 |
Telomere C-strand (Lagging Strand) Synthesis | 34 | 3.33e-01 | 9.59e-02 | 7.12e-01 |
RAS processing | 24 | 4.16e-01 | 9.58e-02 | 7.68e-01 |
FGFRL1 modulation of FGFR1 signaling | 13 | 5.51e-01 | 9.54e-02 | 8.30e-01 |
Formation of the nephric duct | 18 | 4.84e-01 | -9.54e-02 | 8.03e-01 |
TGF-beta receptor signaling activates SMADs | 47 | 2.58e-01 | -9.53e-02 | 6.51e-01 |
Formation of the ternary complex, and subsequently, the 43S complex | 50 | 2.44e-01 | 9.52e-02 | 6.42e-01 |
ARMS-mediated activation | 7 | 6.63e-01 | -9.52e-02 | 8.80e-01 |
Collagen chain trimerization | 44 | 2.76e-01 | -9.49e-02 | 6.72e-01 |
Metallothioneins bind metals | 11 | 5.86e-01 | -9.48e-02 | 8.50e-01 |
Mismatch Repair | 15 | 5.25e-01 | 9.48e-02 | 8.19e-01 |
Signaling by CSF1 (M-CSF) in myeloid cells | 31 | 3.61e-01 | 9.48e-02 | 7.30e-01 |
RHO GTPases Activate WASPs and WAVEs | 36 | 3.26e-01 | -9.46e-02 | 7.07e-01 |
Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) | 8 | 6.43e-01 | 9.46e-02 | 8.75e-01 |
Uptake and actions of bacterial toxins | 28 | 3.88e-01 | -9.43e-02 | 7.51e-01 |
Association of TriC/CCT with target proteins during biosynthesis | 39 | 3.08e-01 | -9.43e-02 | 6.96e-01 |
Negative regulation of MAPK pathway | 43 | 2.85e-01 | -9.42e-02 | 6.77e-01 |
Retinoid metabolism and transport | 44 | 2.80e-01 | -9.41e-02 | 6.74e-01 |
Signaling by FGFR2 | 73 | 1.65e-01 | -9.41e-02 | 5.78e-01 |
Signaling by PDGFR in disease | 20 | 4.67e-01 | -9.39e-02 | 7.95e-01 |
Signaling by FGFR4 | 41 | 2.99e-01 | -9.37e-02 | 6.86e-01 |
Replacement of protamines by nucleosomes in the male pronucleus | 22 | 4.47e-01 | -9.37e-02 | 7.85e-01 |
Caspase activation via Dependence Receptors in the absence of ligand | 10 | 6.08e-01 | 9.37e-02 | 8.63e-01 |
Termination of translesion DNA synthesis | 32 | 3.60e-01 | 9.36e-02 | 7.29e-01 |
Signaling by Rho GTPases, Miro GTPases and RHOBTB3 | 675 | 3.43e-05 | -9.34e-02 | 5.31e-03 |
Signaling by the B Cell Receptor (BCR) | 110 | 9.05e-02 | 9.34e-02 | 4.60e-01 |
Erythrocytes take up oxygen and release carbon dioxide | 8 | 6.49e-01 | -9.31e-02 | 8.75e-01 |
Synthesis of IP3 and IP4 in the cytosol | 26 | 4.12e-01 | -9.30e-02 | 7.67e-01 |
Defective ST3GAL3 causes MCT12 and EIEE15 | 8 | 6.49e-01 | -9.30e-02 | 8.75e-01 |
PI3K Cascade | 44 | 2.89e-01 | -9.24e-02 | 6.79e-01 |
Abortive elongation of HIV-1 transcript in the absence of Tat | 23 | 4.43e-01 | -9.24e-02 | 7.81e-01 |
Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA | 5 | 7.21e-01 | 9.22e-02 | 8.99e-01 |
TCR signaling | 116 | 8.65e-02 | 9.21e-02 | 4.51e-01 |
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 20 | 4.76e-01 | 9.21e-02 | 7.99e-01 |
Ubiquinol biosynthesis | 8 | 6.52e-01 | -9.20e-02 | 8.75e-01 |
TICAM1-dependent activation of IRF3/IRF7 | 12 | 5.81e-01 | -9.20e-02 | 8.49e-01 |
IRS-related events triggered by IGF1R | 52 | 2.52e-01 | -9.19e-02 | 6.48e-01 |
Fc epsilon receptor (FCERI) signaling | 131 | 6.95e-02 | 9.18e-02 | 4.11e-01 |
2-LTR circle formation | 7 | 6.74e-01 | 9.17e-02 | 8.86e-01 |
Diseases associated with glycosylation precursor biosynthesis | 15 | 5.39e-01 | -9.16e-02 | 8.24e-01 |
Reduction of cytosolic Ca++ levels | 12 | 5.83e-01 | -9.16e-02 | 8.49e-01 |
Diseases of hemostasis | 19 | 4.89e-01 | -9.16e-02 | 8.04e-01 |
Acyl chain remodeling of DAG and TAG | 7 | 6.75e-01 | -9.15e-02 | 8.86e-01 |
RHOG GTPase cycle | 74 | 1.74e-01 | -9.13e-02 | 5.92e-01 |
IRAK4 deficiency (TLR2/4) | 18 | 5.03e-01 | 9.13e-02 | 8.13e-01 |
Mitochondrial Fatty Acid Beta-Oxidation | 37 | 3.37e-01 | -9.12e-02 | 7.12e-01 |
Potassium Channels | 103 | 1.10e-01 | 9.12e-02 | 4.93e-01 |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 25 | 4.30e-01 | 9.12e-02 | 7.77e-01 |
Free fatty acid receptors | 5 | 7.24e-01 | 9.12e-02 | 8.99e-01 |
Acetylcholine Neurotransmitter Release Cycle | 17 | 5.16e-01 | 9.11e-02 | 8.15e-01 |
SUMOylation of transcription cofactors | 44 | 2.97e-01 | -9.09e-02 | 6.84e-01 |
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 16 | 5.29e-01 | -9.08e-02 | 8.21e-01 |
Collagen degradation | 63 | 2.13e-01 | -9.08e-02 | 6.18e-01 |
Diseases associated with surfactant metabolism | 9 | 6.37e-01 | -9.08e-02 | 8.73e-01 |
Metabolism of lipids | 754 | 2.32e-05 | -9.05e-02 | 4.88e-03 |
Post-translational modification: synthesis of GPI-anchored proteins | 93 | 1.32e-01 | 9.03e-02 | 5.15e-01 |
Cargo recognition for clathrin-mediated endocytosis | 104 | 1.12e-01 | -9.02e-02 | 4.95e-01 |
Glutathione conjugation | 36 | 3.49e-01 | -9.02e-02 | 7.17e-01 |
RSV-host interactions | 92 | 1.36e-01 | 9.00e-02 | 5.25e-01 |
Resolution of D-loop Structures through Holliday Junction Intermediates | 32 | 3.78e-01 | 9.00e-02 | 7.48e-01 |
Defective GALNT12 causes CRCS1 | 18 | 5.09e-01 | 8.99e-02 | 8.13e-01 |
RHOD GTPase cycle | 52 | 2.63e-01 | -8.97e-02 | 6.59e-01 |
cGMP effects | 16 | 5.36e-01 | 8.94e-02 | 8.22e-01 |
G-protein beta:gamma signalling | 32 | 3.83e-01 | -8.92e-02 | 7.51e-01 |
Cargo trafficking to the periciliary membrane | 51 | 2.71e-01 | 8.91e-02 | 6.68e-01 |
Mitochondrial calcium ion transport | 21 | 4.80e-01 | -8.91e-02 | 8.02e-01 |
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 106 | 1.14e-01 | -8.89e-02 | 4.97e-01 |
Extracellular matrix organization | 299 | 8.20e-03 | -8.88e-02 | 1.67e-01 |
Myoclonic epilepsy of Lafora | 9 | 6.44e-01 | 8.88e-02 | 8.75e-01 |
Transport and synthesis of PAPS | 6 | 7.06e-01 | -8.88e-02 | 8.92e-01 |
Activated point mutants of FGFR2 | 17 | 5.26e-01 | 8.88e-02 | 8.19e-01 |
Influenza Viral RNA Transcription and Replication | 136 | 7.46e-02 | 8.85e-02 | 4.28e-01 |
Glycolysis | 74 | 1.89e-01 | -8.84e-02 | 6.01e-01 |
G beta:gamma signalling through BTK | 18 | 5.16e-01 | -8.84e-02 | 8.15e-01 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 95 | 1.37e-01 | 8.83e-02 | 5.25e-01 |
N-Glycan antennae elongation | 15 | 5.54e-01 | 8.82e-02 | 8.32e-01 |
MyD88 deficiency (TLR2/4) | 17 | 5.30e-01 | 8.79e-02 | 8.21e-01 |
Downregulation of SMAD2/3:SMAD4 transcriptional activity | 31 | 3.98e-01 | 8.76e-02 | 7.57e-01 |
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 17 | 5.33e-01 | -8.74e-02 | 8.21e-01 |
Diseases of programmed cell death | 68 | 2.13e-01 | -8.72e-02 | 6.18e-01 |
Cell Cycle Checkpoints | 268 | 1.40e-02 | 8.72e-02 | 2.18e-01 |
Downstream signaling of activated FGFR4 | 27 | 4.33e-01 | -8.71e-02 | 7.77e-01 |
PI3K/AKT Signaling in Cancer | 105 | 1.24e-01 | -8.70e-02 | 5.07e-01 |
Positive epigenetic regulation of rRNA expression | 69 | 2.12e-01 | -8.69e-02 | 6.18e-01 |
Anti-inflammatory response favouring Leishmania parasite infection | 77 | 1.88e-01 | -8.68e-02 | 6.01e-01 |
Leishmania parasite growth and survival | 77 | 1.88e-01 | -8.68e-02 | 6.01e-01 |
Maturation of nucleoprotein 9683610 | 11 | 6.18e-01 | -8.68e-02 | 8.63e-01 |
TRP channels | 28 | 4.27e-01 | 8.66e-02 | 7.75e-01 |
Signaling by Non-Receptor Tyrosine Kinases | 54 | 2.72e-01 | -8.65e-02 | 6.68e-01 |
Signaling by PTK6 | 54 | 2.72e-01 | -8.65e-02 | 6.68e-01 |
HSF1-dependent transactivation | 36 | 3.69e-01 | -8.64e-02 | 7.40e-01 |
Cristae formation | 28 | 4.29e-01 | 8.64e-02 | 7.75e-01 |
Degradation of the extracellular matrix | 139 | 7.90e-02 | -8.63e-02 | 4.38e-01 |
Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 19 | 5.16e-01 | -8.61e-02 | 8.15e-01 |
Cellular response to starvation | 153 | 6.62e-02 | 8.60e-02 | 4.05e-01 |
Aspartate and asparagine metabolism | 11 | 6.22e-01 | 8.58e-02 | 8.63e-01 |
RNA Polymerase III Transcription Termination | 23 | 4.77e-01 | -8.57e-02 | 7.99e-01 |
Nucleotide salvage | 23 | 4.77e-01 | -8.57e-02 | 7.99e-01 |
Peroxisomal protein import | 63 | 2.40e-01 | -8.56e-02 | 6.39e-01 |
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 | 9 | 6.57e-01 | -8.56e-02 | 8.76e-01 |
FRS-mediated FGFR3 signaling | 20 | 5.08e-01 | -8.55e-02 | 8.13e-01 |
Nicotinamide salvaging | 19 | 5.19e-01 | -8.54e-02 | 8.18e-01 |
HDR through Homologous Recombination (HRR) | 66 | 2.31e-01 | 8.52e-02 | 6.31e-01 |
VLDLR internalisation and degradation | 16 | 5.55e-01 | -8.52e-02 | 8.32e-01 |
Epigenetic regulation of gene expression | 149 | 7.29e-02 | -8.51e-02 | 4.25e-01 |
Gap-filling DNA repair synthesis and ligation in GG-NER | 25 | 4.62e-01 | 8.49e-02 | 7.94e-01 |
Glyoxylate metabolism and glycine degradation | 31 | 4.14e-01 | -8.48e-02 | 7.67e-01 |
Regulation of actin dynamics for phagocytic cup formation | 61 | 2.52e-01 | -8.47e-02 | 6.48e-01 |
RUNX3 regulates BCL2L11 (BIM) transcription | 5 | 7.43e-01 | -8.47e-02 | 9.10e-01 |
Triglyceride catabolism | 23 | 4.83e-01 | -8.44e-02 | 8.03e-01 |
The activation of arylsulfatases | 13 | 5.98e-01 | -8.44e-02 | 8.57e-01 |
Ribavirin ADME | 11 | 6.28e-01 | -8.43e-02 | 8.67e-01 |
Meiotic synapsis | 56 | 2.76e-01 | -8.42e-02 | 6.72e-01 |
Cap-dependent Translation Initiation | 118 | 1.14e-01 | 8.41e-02 | 4.97e-01 |
Eukaryotic Translation Initiation | 118 | 1.14e-01 | 8.41e-02 | 4.97e-01 |
Glutamate and glutamine metabolism | 13 | 5.99e-01 | 8.41e-02 | 8.57e-01 |
Effects of PIP2 hydrolysis | 27 | 4.49e-01 | -8.41e-02 | 7.86e-01 |
Transcriptional Regulation by E2F6 | 34 | 3.97e-01 | 8.40e-02 | 7.55e-01 |
Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 10 | 6.46e-01 | 8.39e-02 | 8.75e-01 |
RHOJ GTPase cycle | 54 | 2.87e-01 | -8.37e-02 | 6.77e-01 |
AMPK inhibits chREBP transcriptional activation activity | 8 | 6.82e-01 | 8.35e-02 | 8.86e-01 |
Protein repair | 6 | 7.23e-01 | 8.35e-02 | 8.99e-01 |
Regulation of mRNA stability by proteins that bind AU-rich elements | 89 | 1.75e-01 | 8.32e-02 | 5.92e-01 |
Cobalamin (Cbl) metabolism | 7 | 7.03e-01 | 8.32e-02 | 8.91e-01 |
Costimulation by the CD28 family | 66 | 2.43e-01 | -8.32e-02 | 6.40e-01 |
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models | 22 | 5.01e-01 | -8.28e-02 | 8.13e-01 |
Neurodegenerative Diseases | 22 | 5.01e-01 | -8.28e-02 | 8.13e-01 |
NFE2L2 regulating anti-oxidant/detoxification enzymes | 19 | 5.33e-01 | -8.27e-02 | 8.21e-01 |
RNA Polymerase I Promoter Clearance | 72 | 2.26e-01 | -8.25e-02 | 6.26e-01 |
RNA Polymerase I Transcription | 72 | 2.26e-01 | -8.25e-02 | 6.26e-01 |
Keratan sulfate biosynthesis | 28 | 4.51e-01 | -8.23e-02 | 7.87e-01 |
Triglyceride metabolism | 37 | 3.87e-01 | -8.21e-02 | 7.51e-01 |
Transport of bile salts and organic acids, metal ions and amine compounds | 84 | 1.94e-01 | -8.20e-02 | 6.07e-01 |
MET interacts with TNS proteins | 5 | 7.51e-01 | -8.20e-02 | 9.14e-01 |
Signaling by FGFR1 | 52 | 3.11e-01 | -8.12e-02 | 6.98e-01 |
Late endosomal microautophagy | 34 | 4.13e-01 | -8.12e-02 | 7.67e-01 |
Lysosome Vesicle Biogenesis | 34 | 4.14e-01 | -8.10e-02 | 7.67e-01 |
Negative regulation of TCF-dependent signaling by WNT ligand antagonists | 15 | 5.88e-01 | -8.09e-02 | 8.51e-01 |
Propionyl-CoA catabolism | 5 | 7.54e-01 | 8.08e-02 | 9.17e-01 |
MyD88 cascade initiated on plasma membrane | 96 | 1.71e-01 | -8.08e-02 | 5.88e-01 |
Toll Like Receptor 10 (TLR10) Cascade | 96 | 1.71e-01 | -8.08e-02 | 5.88e-01 |
Toll Like Receptor 5 (TLR5) Cascade | 96 | 1.71e-01 | -8.08e-02 | 5.88e-01 |
HCMV Late Events | 82 | 2.07e-01 | -8.07e-02 | 6.09e-01 |
Killing mechanisms | 12 | 6.29e-01 | 8.06e-02 | 8.67e-01 |
WNT5:FZD7-mediated leishmania damping | 12 | 6.29e-01 | 8.06e-02 | 8.67e-01 |
Influenza Infection | 155 | 8.44e-02 | 8.03e-02 | 4.50e-01 |
Dual Incision in GG-NER | 40 | 3.80e-01 | 8.03e-02 | 7.48e-01 |
Respiratory electron transport | 93 | 1.81e-01 | 8.02e-02 | 5.96e-01 |
Interferon gamma signaling | 94 | 1.79e-01 | -8.01e-02 | 5.94e-01 |
Gap junction trafficking and regulation | 49 | 3.32e-01 | -8.01e-02 | 7.12e-01 |
GTP hydrolysis and joining of the 60S ribosomal subunit | 111 | 1.45e-01 | 8.00e-02 | 5.42e-01 |
STAT5 activation downstream of FLT3 ITD mutants | 10 | 6.61e-01 | -8.00e-02 | 8.80e-01 |
Metabolism of fat-soluble vitamins | 48 | 3.38e-01 | -7.99e-02 | 7.12e-01 |
TRAF6-mediated induction of TAK1 complex within TLR4 complex | 16 | 5.80e-01 | 7.98e-02 | 8.49e-01 |
PERK regulates gene expression | 32 | 4.36e-01 | 7.95e-02 | 7.77e-01 |
Membrane Trafficking | 626 | 6.81e-04 | -7.95e-02 | 5.27e-02 |
MECP2 regulates transcription of neuronal ligands | 8 | 6.98e-01 | 7.93e-02 | 8.90e-01 |
Amino acid transport across the plasma membrane | 33 | 4.31e-01 | -7.92e-02 | 7.77e-01 |
SARS-CoV-2 modulates host translation machinery | 49 | 3.38e-01 | 7.92e-02 | 7.12e-01 |
Protein folding | 97 | 1.78e-01 | -7.92e-02 | 5.92e-01 |
L13a-mediated translational silencing of Ceruloplasmin expression | 110 | 1.52e-01 | 7.91e-02 | 5.54e-01 |
Adherens junctions interactions | 59 | 2.94e-01 | -7.90e-02 | 6.83e-01 |
Formation of axial mesoderm | 14 | 6.09e-01 | -7.88e-02 | 8.63e-01 |
Estrogen-dependent gene expression | 116 | 1.43e-01 | -7.88e-02 | 5.37e-01 |
ROS and RNS production in phagocytes | 35 | 4.21e-01 | 7.86e-02 | 7.69e-01 |
SUMO is transferred from E1 to E2 (UBE2I, UBC9) | 7 | 7.19e-01 | 7.85e-02 | 8.99e-01 |
RUNX1 regulates transcription of genes involved in differentiation of HSCs | 93 | 1.91e-01 | 7.85e-02 | 6.05e-01 |
Defective CHST14 causes EDS, musculocontractural type | 8 | 7.01e-01 | 7.84e-02 | 8.91e-01 |
Triglyceride biosynthesis | 14 | 6.12e-01 | -7.82e-02 | 8.63e-01 |
DNA Damage Bypass | 47 | 3.54e-01 | 7.82e-02 | 7.19e-01 |
IGF1R signaling cascade | 53 | 3.25e-01 | -7.82e-02 | 7.07e-01 |
Uptake of dietary cobalamins into enterocytes | 9 | 6.85e-01 | 7.81e-02 | 8.86e-01 |
Calcineurin activates NFAT | 9 | 6.85e-01 | 7.81e-02 | 8.86e-01 |
RNA Polymerase III Abortive And Retractive Initiation | 41 | 3.87e-01 | -7.80e-02 | 7.51e-01 |
RNA Polymerase III Transcription | 41 | 3.87e-01 | -7.80e-02 | 7.51e-01 |
FGFR2c ligand binding and activation | 13 | 6.27e-01 | 7.78e-02 | 8.67e-01 |
Gastrulation | 127 | 1.31e-01 | 7.76e-02 | 5.13e-01 |
Defective GALNT3 causes HFTC | 18 | 5.69e-01 | 7.75e-02 | 8.44e-01 |
Vitamin B5 (pantothenate) metabolism | 20 | 5.49e-01 | 7.74e-02 | 8.30e-01 |
Activation of GABAB receptors | 43 | 3.80e-01 | -7.73e-02 | 7.48e-01 |
GABA B receptor activation | 43 | 3.80e-01 | -7.73e-02 | 7.48e-01 |
Regulation of NPAS4 gene transcription | 5 | 7.65e-01 | 7.72e-02 | 9.20e-01 |
G beta:gamma signalling through CDC42 | 20 | 5.50e-01 | -7.71e-02 | 8.30e-01 |
Synthesis of 15-eicosatetraenoic acid derivatives | 6 | 7.44e-01 | -7.71e-02 | 9.10e-01 |
Fibronectin matrix formation | 6 | 7.44e-01 | 7.70e-02 | 9.10e-01 |
Chaperonin-mediated protein folding | 91 | 2.05e-01 | -7.69e-02 | 6.08e-01 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 24 | 5.15e-01 | 7.68e-02 | 8.15e-01 |
Synthesis of GDP-mannose | 5 | 7.66e-01 | -7.68e-02 | 9.20e-01 |
Defective Intrinsic Pathway for Apoptosis | 25 | 5.07e-01 | -7.67e-02 | 8.13e-01 |
RHOBTB3 ATPase cycle | 10 | 6.75e-01 | 7.67e-02 | 8.86e-01 |
Cyclin A/B1/B2 associated events during G2/M transition | 24 | 5.16e-01 | 7.66e-02 | 8.15e-01 |
HATs acetylate histones | 104 | 1.78e-01 | -7.64e-02 | 5.92e-01 |
Clathrin-mediated endocytosis | 144 | 1.14e-01 | -7.63e-02 | 4.97e-01 |
Defective CSF2RA causes SMDP4 | 7 | 7.27e-01 | -7.63e-02 | 9.00e-01 |
Defective CSF2RB causes SMDP5 | 7 | 7.27e-01 | -7.63e-02 | 9.00e-01 |
Serotonin Neurotransmitter Release Cycle | 18 | 5.76e-01 | 7.62e-02 | 8.48e-01 |
Mitotic Metaphase and Anaphase | 233 | 4.50e-02 | 7.62e-02 | 3.67e-01 |
tRNA processing | 109 | 1.70e-01 | 7.61e-02 | 5.87e-01 |
N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 35 | 4.37e-01 | 7.59e-02 | 7.77e-01 |
Atorvastatin ADME | 9 | 6.95e-01 | 7.54e-02 | 8.90e-01 |
Glycogen synthesis | 14 | 6.26e-01 | 7.52e-02 | 8.66e-01 |
SARS-CoV-1 targets host intracellular signalling and regulatory pathways | 16 | 6.03e-01 | -7.51e-02 | 8.59e-01 |
Chromatin modifications during the maternal to zygotic transition (MZT) | 33 | 4.56e-01 | -7.50e-02 | 7.90e-01 |
RHOH GTPase cycle | 36 | 4.37e-01 | -7.49e-02 | 7.77e-01 |
Presynaptic nicotinic acetylcholine receptors | 12 | 6.54e-01 | 7.48e-02 | 8.76e-01 |
GPCR ligand binding | 461 | 5.94e-03 | 7.47e-02 | 1.46e-01 |
Norepinephrine Neurotransmitter Release Cycle | 18 | 5.84e-01 | 7.46e-02 | 8.49e-01 |
Suppression of apoptosis | 7 | 7.33e-01 | -7.44e-02 | 9.04e-01 |
Transcriptional regulation of pluripotent stem cells | 29 | 4.89e-01 | 7.43e-02 | 8.04e-01 |
Mitotic Anaphase | 232 | 5.13e-02 | 7.42e-02 | 3.79e-01 |
Vesicle-mediated transport | 664 | 1.09e-03 | -7.42e-02 | 7.08e-02 |
Recognition of DNA damage by PCNA-containing replication complex | 30 | 4.83e-01 | 7.40e-02 | 8.03e-01 |
Vasopressin-like receptors | 6 | 7.54e-01 | -7.40e-02 | 9.16e-01 |
Relaxin receptors | 8 | 7.18e-01 | 7.39e-02 | 8.99e-01 |
NF-kB is activated and signals survival | 13 | 6.45e-01 | -7.37e-02 | 8.75e-01 |
FRS-mediated FGFR4 signaling | 22 | 5.50e-01 | -7.36e-02 | 8.30e-01 |
Peptide ligand-binding receptors | 196 | 7.58e-02 | 7.35e-02 | 4.31e-01 |
MyD88-independent TLR4 cascade | 108 | 1.88e-01 | -7.34e-02 | 6.01e-01 |
TRIF(TICAM1)-mediated TLR4 signaling | 108 | 1.88e-01 | -7.34e-02 | 6.01e-01 |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 56 | 3.43e-01 | -7.32e-02 | 7.12e-01 |
Class B/2 (Secretin family receptors) | 93 | 2.23e-01 | 7.32e-02 | 6.26e-01 |
Defective pyroptosis | 36 | 4.48e-01 | -7.31e-02 | 7.86e-01 |
Maturation of nucleoprotein 9694631 | 15 | 6.24e-01 | -7.31e-02 | 8.64e-01 |
Processive synthesis on the C-strand of the telomere | 19 | 5.84e-01 | 7.25e-02 | 8.49e-01 |
Mitochondrial RNA degradation | 10 | 6.91e-01 | 7.25e-02 | 8.89e-01 |
RA biosynthesis pathway | 22 | 5.56e-01 | 7.25e-02 | 8.33e-01 |
Transport of connexons to the plasma membrane | 19 | 5.84e-01 | 7.25e-02 | 8.49e-01 |
Inhibition of DNA recombination at telomere | 44 | 4.06e-01 | -7.23e-02 | 7.67e-01 |
Defective B4GALT7 causes EDS, progeroid type | 20 | 5.76e-01 | -7.23e-02 | 8.48e-01 |
Deactivation of the beta-catenin transactivating complex | 41 | 4.23e-01 | -7.22e-02 | 7.69e-01 |
Extension of Telomeres | 51 | 3.73e-01 | 7.21e-02 | 7.44e-01 |
Biotin transport and metabolism | 11 | 6.79e-01 | -7.20e-02 | 8.86e-01 |
Regulation of gene expression in beta cells | 21 | 5.68e-01 | 7.19e-02 | 8.44e-01 |
Regulation of KIT signaling | 16 | 6.19e-01 | -7.19e-02 | 8.63e-01 |
Programmed Cell Death | 209 | 7.41e-02 | -7.17e-02 | 4.27e-01 |
Defective CHST6 causes MCDC1 | 8 | 7.26e-01 | -7.16e-02 | 9.00e-01 |
Metabolism of amine-derived hormones | 17 | 6.10e-01 | 7.15e-02 | 8.63e-01 |
tRNA processing in the nucleus | 59 | 3.43e-01 | 7.14e-02 | 7.12e-01 |
RAS signaling downstream of NF1 loss-of-function variants | 7 | 7.44e-01 | 7.13e-02 | 9.10e-01 |
Formation of apoptosome | 11 | 6.83e-01 | -7.11e-02 | 8.86e-01 |
Regulation of the apoptosome activity | 11 | 6.83e-01 | -7.11e-02 | 8.86e-01 |
Ovarian tumor domain proteases | 39 | 4.43e-01 | -7.11e-02 | 7.81e-01 |
VEGF binds to VEGFR leading to receptor dimerization | 8 | 7.28e-01 | -7.10e-02 | 9.00e-01 |
VEGF ligand-receptor interactions | 8 | 7.28e-01 | -7.10e-02 | 9.00e-01 |
Rap1 signalling | 16 | 6.24e-01 | -7.08e-02 | 8.64e-01 |
Retrograde transport at the Trans-Golgi-Network | 49 | 3.91e-01 | -7.08e-02 | 7.54e-01 |
Depolymerization of the Nuclear Lamina | 15 | 6.36e-01 | 7.06e-02 | 8.72e-01 |
Global Genome Nucleotide Excision Repair (GG-NER) | 83 | 2.67e-01 | 7.05e-02 | 6.66e-01 |
Signaling by Insulin receptor | 81 | 2.73e-01 | -7.04e-02 | 6.69e-01 |
Signaling by FGFR in disease | 63 | 3.34e-01 | -7.03e-02 | 7.12e-01 |
Resolution of D-Loop Structures | 33 | 4.84e-01 | 7.03e-02 | 8.03e-01 |
Signaling by NOTCH1 | 74 | 2.96e-01 | -7.03e-02 | 6.84e-01 |
Metabolism of water-soluble vitamins and cofactors | 126 | 1.73e-01 | -7.03e-02 | 5.90e-01 |
Defective binding of VWF variant to GPIb:IX:V | 7 | 7.48e-01 | -7.01e-02 | 9.12e-01 |
Enhanced binding of GP1BA variant to VWF multimer:collagen | 7 | 7.48e-01 | -7.01e-02 | 9.12e-01 |
NPAS4 regulates expression of target genes | 21 | 5.81e-01 | 6.97e-02 | 8.49e-01 |
ER-Phagosome pathway | 91 | 2.51e-01 | 6.96e-02 | 6.48e-01 |
Phosphorylation of CD3 and TCR zeta chains | 20 | 5.90e-01 | 6.96e-02 | 8.53e-01 |
Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA | 6 | 7.69e-01 | -6.93e-02 | 9.21e-01 |
Downstream signaling of activated FGFR1 | 31 | 5.06e-01 | -6.90e-02 | 8.13e-01 |
ER to Golgi Anterograde Transport | 153 | 1.41e-01 | -6.89e-02 | 5.35e-01 |
SLC transporter disorders | 99 | 2.37e-01 | -6.88e-02 | 6.36e-01 |
Diseases of glycosylation | 145 | 1.54e-01 | -6.86e-02 | 5.54e-01 |
RAC3 GTPase cycle | 94 | 2.50e-01 | -6.86e-02 | 6.47e-01 |
Reactions specific to the complex N-glycan synthesis pathway | 10 | 7.07e-01 | -6.86e-02 | 8.92e-01 |
Loss of Nlp from mitotic centrosomes | 69 | 3.25e-01 | -6.85e-02 | 7.07e-01 |
Loss of proteins required for interphase microtubule organization from the centrosome | 69 | 3.25e-01 | -6.85e-02 | 7.07e-01 |
Interactions of Vpr with host cellular proteins | 36 | 4.78e-01 | 6.83e-02 | 8.00e-01 |
SLC-mediated transmembrane transport | 247 | 6.50e-02 | -6.81e-02 | 4.02e-01 |
NOTCH1 Intracellular Domain Regulates Transcription | 48 | 4.15e-01 | -6.81e-02 | 7.67e-01 |
Golgi-to-ER retrograde transport | 133 | 1.76e-01 | -6.79e-02 | 5.92e-01 |
Negative regulation of FGFR3 signaling | 29 | 5.27e-01 | -6.79e-02 | 8.19e-01 |
PI-3K cascade:FGFR3 | 18 | 6.19e-01 | -6.77e-02 | 8.63e-01 |
Synthesis of bile acids and bile salts | 34 | 4.95e-01 | 6.76e-02 | 8.10e-01 |
Metabolism of steroids | 155 | 1.47e-01 | -6.74e-02 | 5.46e-01 |
Glutamate Neurotransmitter Release Cycle | 24 | 5.68e-01 | 6.74e-02 | 8.44e-01 |
Metabolism of vitamins and cofactors | 191 | 1.08e-01 | -6.74e-02 | 4.92e-01 |
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 15 | 6.52e-01 | 6.73e-02 | 8.75e-01 |
Synthesis of PIPs at the ER membrane | 5 | 7.95e-01 | -6.73e-02 | 9.35e-01 |
Protein hydroxylation | 18 | 6.21e-01 | -6.72e-02 | 8.63e-01 |
Amyloid fiber formation | 74 | 3.18e-01 | -6.71e-02 | 7.03e-01 |
Formation of xylulose-5-phosphate | 5 | 7.95e-01 | -6.71e-02 | 9.36e-01 |
ER Quality Control Compartment (ERQC) | 21 | 5.95e-01 | 6.70e-02 | 8.57e-01 |
C-type lectin receptors (CLRs) | 142 | 1.69e-01 | 6.69e-02 | 5.85e-01 |
Glycosphingolipid catabolism | 39 | 4.70e-01 | -6.68e-02 | 7.95e-01 |
Cleavage of the damaged purine | 33 | 5.07e-01 | -6.67e-02 | 8.13e-01 |
Depurination | 33 | 5.07e-01 | -6.67e-02 | 8.13e-01 |
Recognition and association of DNA glycosylase with site containing an affected purine | 33 | 5.07e-01 | -6.67e-02 | 8.13e-01 |
FGFR2 mutant receptor activation | 33 | 5.07e-01 | 6.67e-02 | 8.13e-01 |
Cytosolic sensors of pathogen-associated DNA | 64 | 3.56e-01 | -6.67e-02 | 7.23e-01 |
Regulation of insulin secretion | 78 | 3.10e-01 | -6.65e-02 | 6.97e-01 |
Arachidonic acid metabolism | 59 | 3.78e-01 | 6.63e-02 | 7.48e-01 |
FGFR2 ligand binding and activation | 20 | 6.08e-01 | 6.63e-02 | 8.63e-01 |
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 14 | 6.68e-01 | 6.63e-02 | 8.82e-01 |
Neurotransmitter receptors and postsynaptic signal transmission | 203 | 1.04e-01 | 6.63e-02 | 4.85e-01 |
Dermatan sulfate biosynthesis | 11 | 7.04e-01 | 6.62e-02 | 8.91e-01 |
DAP12 signaling | 28 | 5.45e-01 | -6.61e-02 | 8.30e-01 |
Complement cascade | 56 | 3.92e-01 | -6.61e-02 | 7.54e-01 |
Vpr-mediated nuclear import of PICs | 34 | 5.06e-01 | 6.60e-02 | 8.13e-01 |
Hedgehog ‘on’ state | 86 | 2.90e-01 | 6.59e-02 | 6.81e-01 |
ALK mutants bind TKIs | 12 | 6.92e-01 | 6.59e-02 | 8.89e-01 |
HCMV Infection | 127 | 2.00e-01 | -6.58e-02 | 6.08e-01 |
Cytochrome c-mediated apoptotic response | 13 | 6.82e-01 | -6.56e-02 | 8.86e-01 |
SARS-CoV-2 modulates autophagy | 11 | 7.07e-01 | 6.55e-02 | 8.92e-01 |
Post-translational protein phosphorylation | 105 | 2.46e-01 | -6.55e-02 | 6.42e-01 |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 22 | 5.96e-01 | 6.53e-02 | 8.57e-01 |
Respiratory Syncytial Virus Infection Pathway | 114 | 2.30e-01 | 6.51e-02 | 6.30e-01 |
Signaling by Receptor Tyrosine Kinases | 527 | 1.05e-02 | -6.51e-02 | 1.93e-01 |
Metabolism of folate and pterines | 17 | 6.43e-01 | -6.48e-02 | 8.75e-01 |
Defective B3GAT3 causes JDSSDHD | 20 | 6.16e-01 | -6.48e-02 | 8.63e-01 |
Diseases associated with O-glycosylation of proteins | 70 | 3.48e-01 | -6.48e-02 | 7.17e-01 |
Formation of Fibrin Clot (Clotting Cascade) | 39 | 4.86e-01 | -6.44e-02 | 8.03e-01 |
Alpha-oxidation of phytanate | 6 | 7.85e-01 | -6.44e-02 | 9.32e-01 |
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 16 | 6.56e-01 | 6.44e-02 | 8.76e-01 |
Diseases associated with the TLR signaling cascade | 31 | 5.35e-01 | -6.44e-02 | 8.21e-01 |
Diseases of Immune System | 31 | 5.35e-01 | -6.44e-02 | 8.21e-01 |
Surfactant metabolism | 27 | 5.63e-01 | 6.43e-02 | 8.40e-01 |
Neuronal System | 410 | 2.55e-02 | 6.43e-02 | 2.83e-01 |
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 54 | 4.15e-01 | -6.41e-02 | 7.67e-01 |
Other interleukin signaling | 24 | 5.88e-01 | -6.39e-02 | 8.51e-01 |
Pyruvate metabolism and Citric Acid (TCA) cycle | 55 | 4.13e-01 | -6.38e-02 | 7.67e-01 |
Defects of platelet adhesion to exposed collagen | 8 | 7.55e-01 | -6.36e-02 | 9.17e-01 |
Gap junction trafficking | 47 | 4.51e-01 | -6.35e-02 | 7.87e-01 |
Transmission across Chemical Synapses | 268 | 7.36e-02 | 6.35e-02 | 4.26e-01 |
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 22 | 6.06e-01 | -6.35e-02 | 8.62e-01 |
Telomere Extension By Telomerase | 23 | 5.98e-01 | 6.35e-02 | 8.57e-01 |
MAP2K and MAPK activation | 40 | 4.88e-01 | -6.34e-02 | 8.04e-01 |
WNT ligand biogenesis and trafficking | 26 | 5.76e-01 | -6.34e-02 | 8.48e-01 |
Ion transport by P-type ATPases | 55 | 4.17e-01 | -6.33e-02 | 7.68e-01 |
Miscellaneous transport and binding events | 26 | 5.77e-01 | 6.32e-02 | 8.48e-01 |
Protein ubiquitination | 76 | 3.41e-01 | 6.31e-02 | 7.12e-01 |
RNA Polymerase I Transcription Initiation | 46 | 4.59e-01 | -6.31e-02 | 7.92e-01 |
Transport of nucleotide sugars | 9 | 7.43e-01 | -6.31e-02 | 9.10e-01 |
PD-1 signaling | 21 | 6.17e-01 | 6.30e-02 | 8.63e-01 |
Lectin pathway of complement activation | 8 | 7.58e-01 | -6.30e-02 | 9.18e-01 |
Aberrant regulation of mitotic cell cycle due to RB1 defects | 36 | 5.14e-01 | 6.29e-02 | 8.15e-01 |
Toll Like Receptor 3 (TLR3) Cascade | 104 | 2.68e-01 | -6.29e-02 | 6.66e-01 |
DNA Double Strand Break Response | 57 | 4.13e-01 | -6.27e-02 | 7.67e-01 |
Resolution of Abasic Sites (AP sites) | 38 | 5.03e-01 | 6.27e-02 | 8.13e-01 |
FGFR3 ligand binding and activation | 13 | 6.95e-01 | -6.27e-02 | 8.90e-01 |
FGFR3c ligand binding and activation | 13 | 6.95e-01 | -6.27e-02 | 8.90e-01 |
CLEC7A (Dectin-1) induces NFAT activation | 11 | 7.19e-01 | 6.26e-02 | 8.99e-01 |
Processive synthesis on the lagging strand | 15 | 6.75e-01 | 6.26e-02 | 8.86e-01 |
Synthesis of PIPs at the plasma membrane | 53 | 4.31e-01 | -6.25e-02 | 7.77e-01 |
GPVI-mediated activation cascade | 34 | 5.32e-01 | -6.19e-02 | 8.21e-01 |
MAPK targets/ Nuclear events mediated by MAP kinases | 31 | 5.51e-01 | 6.18e-02 | 8.30e-01 |
Cytosolic sulfonation of small molecules | 22 | 6.18e-01 | -6.15e-02 | 8.63e-01 |
Negative regulation of FLT3 | 15 | 6.81e-01 | 6.14e-02 | 8.86e-01 |
Mitochondrial translation termination | 87 | 3.23e-01 | 6.13e-02 | 7.07e-01 |
Biological oxidations | 216 | 1.22e-01 | 6.11e-02 | 5.02e-01 |
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 30 | 5.65e-01 | 6.07e-02 | 8.41e-01 |
Negative regulation of FGFR4 signaling | 31 | 5.59e-01 | -6.06e-02 | 8.35e-01 |
COPI-dependent Golgi-to-ER retrograde traffic | 99 | 2.98e-01 | -6.05e-02 | 6.84e-01 |
Signaling by NOTCH | 211 | 1.30e-01 | -6.04e-02 | 5.13e-01 |
NCAM1 interactions | 42 | 4.99e-01 | -6.03e-02 | 8.12e-01 |
rRNA processing in the nucleus and cytosol | 190 | 1.52e-01 | 6.02e-02 | 5.54e-01 |
p75NTR signals via NF-kB | 16 | 6.77e-01 | -6.02e-02 | 8.86e-01 |
mRNA decay by 5’ to 3’ exoribonuclease | 15 | 6.87e-01 | 6.00e-02 | 8.87e-01 |
Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | 30 | 5.70e-01 | -6.00e-02 | 8.44e-01 |
Serine biosynthesis | 9 | 7.57e-01 | 5.96e-02 | 9.18e-01 |
Cleavage of the damaged pyrimidine | 38 | 5.26e-01 | -5.94e-02 | 8.19e-01 |
Depyrimidination | 38 | 5.26e-01 | -5.94e-02 | 8.19e-01 |
Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 38 | 5.26e-01 | -5.94e-02 | 8.19e-01 |
Formation of the cornified envelope | 125 | 2.54e-01 | 5.91e-02 | 6.48e-01 |
Platelet activation, signaling and aggregation | 259 | 1.02e-01 | -5.89e-02 | 4.82e-01 |
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 14 | 7.03e-01 | 5.88e-02 | 8.91e-01 |
Ca2+ pathway | 62 | 4.23e-01 | -5.88e-02 | 7.69e-01 |
rRNA processing | 200 | 1.53e-01 | 5.86e-02 | 5.54e-01 |
CREB3 factors activate genes | 9 | 7.61e-01 | -5.85e-02 | 9.20e-01 |
Signaling by WNT | 293 | 8.60e-02 | -5.83e-02 | 4.50e-01 |
Regulation of Complement cascade | 45 | 4.99e-01 | -5.82e-02 | 8.12e-01 |
EPHA-mediated growth cone collapse | 29 | 5.88e-01 | -5.81e-02 | 8.51e-01 |
SARS-CoV-2 activates/modulates innate and adaptive immune responses | 121 | 2.71e-01 | 5.80e-02 | 6.68e-01 |
Antigen processing-Cross presentation | 105 | 3.05e-01 | 5.79e-02 | 6.91e-01 |
Calnexin/calreticulin cycle | 26 | 6.09e-01 | 5.79e-02 | 8.63e-01 |
Bacterial Infection Pathways | 69 | 4.06e-01 | -5.78e-02 | 7.67e-01 |
Interleukin-3, Interleukin-5 and GM-CSF signaling | 45 | 5.03e-01 | -5.78e-02 | 8.13e-01 |
TP53 Regulates Transcription of DNA Repair Genes | 61 | 4.35e-01 | 5.77e-02 | 7.77e-01 |
RHOBTB GTPase Cycle | 35 | 5.55e-01 | 5.76e-02 | 8.32e-01 |
HIV elongation arrest and recovery | 33 | 5.72e-01 | -5.68e-02 | 8.46e-01 |
Pausing and recovery of HIV elongation | 33 | 5.72e-01 | -5.68e-02 | 8.46e-01 |
Trafficking of GluR2-containing AMPA receptors | 17 | 6.85e-01 | -5.68e-02 | 8.86e-01 |
Early SARS-CoV-2 Infection Events | 37 | 5.50e-01 | -5.68e-02 | 8.30e-01 |
Recycling of bile acids and salts | 18 | 6.77e-01 | -5.67e-02 | 8.86e-01 |
Anchoring of the basal body to the plasma membrane | 96 | 3.37e-01 | -5.67e-02 | 7.12e-01 |
Response of Mtb to phagocytosis | 23 | 6.39e-01 | 5.66e-02 | 8.74e-01 |
Tie2 Signaling | 18 | 6.78e-01 | 5.66e-02 | 8.86e-01 |
Synthesis of PA | 38 | 5.47e-01 | -5.65e-02 | 8.30e-01 |
PI-3K cascade:FGFR4 | 20 | 6.62e-01 | -5.65e-02 | 8.80e-01 |
SHC-mediated cascade:FGFR2 | 23 | 6.40e-01 | 5.64e-02 | 8.74e-01 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 115 | 2.97e-01 | 5.62e-02 | 6.84e-01 |
Nonsense-Mediated Decay (NMD) | 115 | 2.97e-01 | 5.62e-02 | 6.84e-01 |
Sensory perception of sweet, bitter, and umami (glutamate) taste | 41 | 5.34e-01 | 5.61e-02 | 8.21e-01 |
Role of ABL in ROBO-SLIT signaling | 8 | 7.84e-01 | -5.60e-02 | 9.31e-01 |
O-glycosylation of TSR domain-containing proteins | 39 | 5.46e-01 | -5.59e-02 | 8.30e-01 |
TNFR2 non-canonical NF-kB pathway | 99 | 3.40e-01 | 5.55e-02 | 7.12e-01 |
Metabolism | 2091 | 2.79e-05 | -5.55e-02 | 5.09e-03 |
Erythropoietin activates RAS | 14 | 7.20e-01 | -5.54e-02 | 8.99e-01 |
Formation of the Editosome | 8 | 7.87e-01 | 5.52e-02 | 9.32e-01 |
mRNA Editing: C to U Conversion | 8 | 7.87e-01 | 5.52e-02 | 9.32e-01 |
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 28 | 6.14e-01 | 5.51e-02 | 8.63e-01 |
Regulation of beta-cell development | 42 | 5.37e-01 | 5.51e-02 | 8.23e-01 |
Intracellular signaling by second messengers | 327 | 8.74e-02 | -5.50e-02 | 4.51e-01 |
SIRT1 negatively regulates rRNA expression | 31 | 5.97e-01 | -5.48e-02 | 8.57e-01 |
Signaling by ERBB4 | 58 | 4.70e-01 | -5.48e-02 | 7.95e-01 |
Mitophagy | 28 | 6.17e-01 | 5.46e-02 | 8.63e-01 |
O-linked glycosylation of mucins | 63 | 4.54e-01 | 5.45e-02 | 7.88e-01 |
HDMs demethylate histones | 21 | 6.66e-01 | -5.45e-02 | 8.81e-01 |
Sperm Motility And Taxes | 9 | 7.77e-01 | 5.44e-02 | 9.26e-01 |
Regulation of signaling by CBL | 22 | 6.59e-01 | 5.44e-02 | 8.78e-01 |
ABC transporters in lipid homeostasis | 18 | 6.90e-01 | 5.43e-02 | 8.89e-01 |
Transcription of the HIV genome | 69 | 4.37e-01 | 5.42e-02 | 7.77e-01 |
Transport to the Golgi and subsequent modification | 184 | 2.06e-01 | -5.40e-02 | 6.09e-01 |
Synthesis of Prostaglandins (PG) and Thromboxanes (TX) | 15 | 7.19e-01 | 5.37e-02 | 8.99e-01 |
Mitotic G2-G2/M phases | 197 | 1.95e-01 | 5.36e-02 | 6.07e-01 |
Translation | 287 | 1.18e-01 | 5.36e-02 | 5.00e-01 |
TICAM1, RIP1-mediated IKK complex recruitment | 19 | 6.87e-01 | 5.35e-02 | 8.87e-01 |
NEP/NS2 Interacts with the Cellular Export Machinery | 32 | 6.01e-01 | 5.34e-02 | 8.58e-01 |
CREB1 phosphorylation through the activation of Adenylate Cyclase | 12 | 7.49e-01 | 5.33e-02 | 9.13e-01 |
Deposition of new CENPA-containing nucleosomes at the centromere | 48 | 5.23e-01 | 5.33e-02 | 8.18e-01 |
Nucleosome assembly | 48 | 5.23e-01 | 5.33e-02 | 8.18e-01 |
Mitochondrial protein import | 62 | 4.70e-01 | 5.30e-02 | 7.95e-01 |
InlB-mediated entry of Listeria monocytogenes into host cell | 15 | 7.23e-01 | 5.29e-02 | 8.99e-01 |
Signaling by Erythropoietin | 25 | 6.48e-01 | -5.28e-02 | 8.75e-01 |
RHOT2 GTPase cycle | 7 | 8.09e-01 | -5.27e-02 | 9.40e-01 |
Resolution of Sister Chromatid Cohesion | 123 | 3.12e-01 | 5.27e-02 | 7.00e-01 |
Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | 16 | 7.15e-01 | -5.27e-02 | 8.99e-01 |
Apoptosis | 178 | 2.25e-01 | -5.27e-02 | 6.26e-01 |
Receptor-type tyrosine-protein phosphatases | 20 | 6.84e-01 | 5.26e-02 | 8.86e-01 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 122 | 3.15e-01 | -5.26e-02 | 7.03e-01 |
Downregulation of ERBB2 signaling | 29 | 6.24e-01 | -5.26e-02 | 8.64e-01 |
mitochondrial fatty acid beta-oxidation of saturated fatty acids | 11 | 7.63e-01 | -5.25e-02 | 9.20e-01 |
Regulation of TP53 Activity | 159 | 2.53e-01 | -5.25e-02 | 6.48e-01 |
Ras activation upon Ca2+ influx through NMDA receptor | 20 | 6.85e-01 | 5.25e-02 | 8.86e-01 |
Diseases of signal transduction by growth factor receptors and second messengers | 457 | 5.51e-02 | -5.23e-02 | 3.87e-01 |
Major pathway of rRNA processing in the nucleolus and cytosol | 180 | 2.26e-01 | 5.23e-02 | 6.26e-01 |
Muscle contraction | 202 | 2.01e-01 | -5.22e-02 | 6.08e-01 |
Infection with Mycobacterium tuberculosis | 26 | 6.45e-01 | 5.22e-02 | 8.75e-01 |
Apoptosis induced DNA fragmentation | 13 | 7.45e-01 | -5.21e-02 | 9.10e-01 |
Chromosome Maintenance | 114 | 3.37e-01 | 5.21e-02 | 7.12e-01 |
Hormone ligand-binding receptors | 13 | 7.45e-01 | -5.20e-02 | 9.10e-01 |
MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 112 | 3.42e-01 | -5.19e-02 | 7.12e-01 |
Toll Like Receptor TLR6:TLR2 Cascade | 112 | 3.42e-01 | -5.19e-02 | 7.12e-01 |
Constitutive Signaling by Aberrant PI3K in Cancer | 78 | 4.28e-01 | -5.19e-02 | 7.75e-01 |
Selenoamino acid metabolism | 115 | 3.37e-01 | 5.18e-02 | 7.12e-01 |
The citric acid (TCA) cycle and respiratory electron transport | 166 | 2.51e-01 | 5.17e-02 | 6.47e-01 |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 56 | 5.06e-01 | -5.13e-02 | 8.13e-01 |
Signal Transduction | 2571 | 2.18e-05 | -5.13e-02 | 4.88e-03 |
RHO GTPase Effectors | 284 | 1.37e-01 | -5.12e-02 | 5.25e-01 |
Oxidative Stress Induced Senescence | 89 | 4.05e-01 | -5.11e-02 | 7.66e-01 |
Synthesis of glycosylphosphatidylinositol (GPI) | 18 | 7.08e-01 | 5.11e-02 | 8.92e-01 |
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 16 | 7.24e-01 | -5.10e-02 | 8.99e-01 |
E3 ubiquitin ligases ubiquitinate target proteins | 56 | 5.10e-01 | 5.09e-02 | 8.15e-01 |
SARS-CoV-1 activates/modulates innate immune responses | 40 | 5.79e-01 | 5.07e-02 | 8.48e-01 |
Interferon Signaling | 260 | 1.60e-01 | -5.06e-02 | 5.65e-01 |
Cellular response to mitochondrial stress | 9 | 7.93e-01 | -5.05e-02 | 9.35e-01 |
SUMO E3 ligases SUMOylate target proteins | 169 | 2.58e-01 | -5.05e-02 | 6.51e-01 |
Host Interactions of HIV factors | 130 | 3.21e-01 | 5.04e-02 | 7.06e-01 |
Transcriptional regulation by RUNX2 | 120 | 3.41e-01 | 5.04e-02 | 7.12e-01 |
Class A/1 (Rhodopsin-like receptors) | 329 | 1.18e-01 | 5.01e-02 | 5.00e-01 |
M-decay: degradation of maternal mRNAs by maternally stored factors | 45 | 5.61e-01 | 5.01e-02 | 8.37e-01 |
G beta:gamma signalling through PLC beta | 20 | 6.98e-01 | -5.01e-02 | 8.90e-01 |
CLEC7A (Dectin-1) signaling | 100 | 3.88e-01 | 5.00e-02 | 7.51e-01 |
Glutamate binding, activation of AMPA receptors and synaptic plasticity | 31 | 6.31e-01 | -4.98e-02 | 8.69e-01 |
Trafficking of AMPA receptors | 31 | 6.31e-01 | -4.98e-02 | 8.69e-01 |
Signaling by ROBO receptors | 217 | 2.07e-01 | 4.97e-02 | 6.09e-01 |
Translation initiation complex formation | 57 | 5.17e-01 | 4.96e-02 | 8.15e-01 |
G2/M Transition | 195 | 2.33e-01 | 4.95e-02 | 6.31e-01 |
mRNA Splicing - Minor Pathway | 53 | 5.33e-01 | 4.95e-02 | 8.21e-01 |
NS1 Mediated Effects on Host Pathways | 41 | 5.86e-01 | 4.91e-02 | 8.50e-01 |
Drug-mediated inhibition of CDK4/CDK6 activity | 5 | 8.49e-01 | -4.91e-02 | 9.65e-01 |
Cytosolic tRNA aminoacylation | 22 | 6.90e-01 | -4.91e-02 | 8.89e-01 |
FLT3 signaling in disease | 28 | 6.53e-01 | -4.91e-02 | 8.75e-01 |
Phospholipase C-mediated cascade; FGFR2 | 18 | 7.20e-01 | 4.88e-02 | 8.99e-01 |
ZBP1(DAI) mediated induction of type I IFNs | 21 | 7.00e-01 | -4.86e-02 | 8.90e-01 |
CD22 mediated BCR regulation | 5 | 8.52e-01 | 4.82e-02 | 9.65e-01 |
Mitotic Prophase | 106 | 3.92e-01 | -4.82e-02 | 7.54e-01 |
DNA Damage Recognition in GG-NER | 38 | 6.07e-01 | 4.82e-02 | 8.63e-01 |
SHC1 events in ERBB4 signaling | 14 | 7.56e-01 | -4.80e-02 | 9.17e-01 |
Cardiac conduction | 130 | 3.46e-01 | 4.79e-02 | 7.15e-01 |
Sealing of the nuclear envelope (NE) by ESCRT-III | 30 | 6.51e-01 | -4.77e-02 | 8.75e-01 |
Fatty acid metabolism | 177 | 2.75e-01 | -4.76e-02 | 6.71e-01 |
Stimuli-sensing channels | 107 | 3.97e-01 | 4.74e-02 | 7.55e-01 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 19 | 7.21e-01 | -4.73e-02 | 8.99e-01 |
Signaling by Ligand-Responsive EGFR Variants in Cancer | 19 | 7.21e-01 | -4.73e-02 | 8.99e-01 |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 58 | 5.34e-01 | 4.72e-02 | 8.21e-01 |
Azathioprine ADME | 23 | 6.96e-01 | -4.71e-02 | 8.90e-01 |
Extrinsic Pathway of Fibrin Clot Formation | 5 | 8.56e-01 | 4.70e-02 | 9.66e-01 |
Mitotic Spindle Checkpoint | 110 | 3.95e-01 | 4.70e-02 | 7.55e-01 |
Transport of inorganic cations/anions and amino acids/oligopeptides | 106 | 4.04e-01 | -4.69e-02 | 7.65e-01 |
Diseases of mitotic cell cycle | 38 | 6.18e-01 | 4.67e-02 | 8.63e-01 |
Platelet homeostasis | 85 | 4.57e-01 | -4.67e-02 | 7.91e-01 |
Interleukin-27 signaling | 11 | 7.90e-01 | 4.63e-02 | 9.34e-01 |
Ribosomal scanning and start codon recognition | 57 | 5.46e-01 | 4.62e-02 | 8.30e-01 |
Diseases of metabolism | 249 | 2.11e-01 | -4.60e-02 | 6.17e-01 |
Fertilization | 26 | 6.85e-01 | 4.60e-02 | 8.86e-01 |
Defective CHSY1 causes TPBS | 8 | 8.23e-01 | 4.57e-02 | 9.47e-01 |
Antiviral mechanism by IFN-stimulated genes | 148 | 3.38e-01 | -4.56e-02 | 7.12e-01 |
Integration of provirus | 9 | 8.14e-01 | 4.53e-02 | 9.42e-01 |
Bile acid and bile salt metabolism | 45 | 6.00e-01 | 4.52e-02 | 8.57e-01 |
Hedgehog ‘off’ state | 112 | 4.10e-01 | 4.51e-02 | 7.67e-01 |
RIPK1-mediated regulated necrosis | 31 | 6.64e-01 | -4.50e-02 | 8.80e-01 |
Regulation of necroptotic cell death | 31 | 6.64e-01 | -4.50e-02 | 8.80e-01 |
Energy dependent regulation of mTOR by LKB1-AMPK | 29 | 6.75e-01 | 4.49e-02 | 8.86e-01 |
Regulation of BACH1 activity | 16 | 7.58e-01 | 4.45e-02 | 9.18e-01 |
Mitochondrial biogenesis | 89 | 4.68e-01 | -4.45e-02 | 7.95e-01 |
Mitochondrial translation initiation | 87 | 4.76e-01 | 4.42e-02 | 7.99e-01 |
Metabolism of steroid hormones | 36 | 6.46e-01 | -4.42e-02 | 8.75e-01 |
RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | 6 | 8.51e-01 | 4.41e-02 | 9.65e-01 |
Activation of kainate receptors upon glutamate binding | 30 | 6.76e-01 | 4.41e-02 | 8.86e-01 |
ATF4 activates genes in response to endoplasmic reticulum stress | 27 | 6.92e-01 | 4.41e-02 | 8.89e-01 |
FGFR2b ligand binding and activation | 10 | 8.10e-01 | -4.40e-02 | 9.40e-01 |
Dual incision in TC-NER | 64 | 5.44e-01 | 4.38e-02 | 8.30e-01 |
Drug ADME | 104 | 4.40e-01 | 4.38e-02 | 7.80e-01 |
Interleukin-10 signaling | 44 | 6.18e-01 | 4.34e-02 | 8.63e-01 |
AURKA Activation by TPX2 | 72 | 5.24e-01 | -4.34e-02 | 8.18e-01 |
Sensory perception of taste | 47 | 6.11e-01 | 4.29e-02 | 8.63e-01 |
Release of Hh-Np from the secreting cell | 8 | 8.34e-01 | -4.29e-02 | 9.55e-01 |
FRS-mediated FGFR1 signaling | 23 | 7.22e-01 | -4.28e-02 | 8.99e-01 |
NRIF signals cell death from the nucleus | 16 | 7.67e-01 | 4.27e-02 | 9.21e-01 |
Negative regulation of NMDA receptor-mediated neuronal transmission | 21 | 7.36e-01 | 4.25e-02 | 9.05e-01 |
Transport of RCbl within the body | 8 | 8.36e-01 | -4.23e-02 | 9.56e-01 |
Linoleic acid (LA) metabolism | 8 | 8.36e-01 | 4.22e-02 | 9.56e-01 |
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 38 | 6.52e-01 | -4.22e-02 | 8.75e-01 |
Interleukin-12 signaling | 43 | 6.32e-01 | -4.22e-02 | 8.69e-01 |
Transport of small molecules | 732 | 5.19e-02 | -4.22e-02 | 3.80e-01 |
Negative regulation of activity of TFAP2 (AP-2) family transcription factors | 10 | 8.18e-01 | -4.21e-02 | 9.45e-01 |
Signaling by BMP | 31 | 6.85e-01 | -4.21e-02 | 8.86e-01 |
GABA receptor activation | 60 | 5.73e-01 | 4.21e-02 | 8.46e-01 |
NOTCH2 Activation and Transmission of Signal to the Nucleus | 22 | 7.33e-01 | -4.20e-02 | 9.04e-01 |
SUMOylation | 175 | 3.38e-01 | -4.19e-02 | 7.12e-01 |
B-WICH complex positively regulates rRNA expression | 54 | 5.95e-01 | -4.18e-02 | 8.57e-01 |
Nucleotide biosynthesis | 12 | 8.03e-01 | 4.16e-02 | 9.39e-01 |
Scavenging by Class B Receptors | 6 | 8.60e-01 | -4.15e-02 | 9.68e-01 |
SUMOylation of ubiquitinylation proteins | 39 | 6.54e-01 | 4.15e-02 | 8.76e-01 |
Intra-Golgi and retrograde Golgi-to-ER traffic | 202 | 3.15e-01 | -4.10e-02 | 7.03e-01 |
MHC class II antigen presentation | 123 | 4.34e-01 | -4.08e-02 | 7.77e-01 |
Toll Like Receptor 2 (TLR2) Cascade | 115 | 4.49e-01 | -4.08e-02 | 7.86e-01 |
Toll Like Receptor TLR1:TLR2 Cascade | 115 | 4.49e-01 | -4.08e-02 | 7.86e-01 |
ADP signalling through P2Y purinoceptor 12 | 22 | 7.40e-01 | -4.08e-02 | 9.10e-01 |
Translation of Structural Proteins 9683701 | 29 | 7.04e-01 | -4.08e-02 | 8.91e-01 |
Nuclear Envelope Breakdown | 53 | 6.09e-01 | 4.06e-02 | 8.63e-01 |
Nuclear import of Rev protein | 34 | 6.84e-01 | 4.04e-02 | 8.86e-01 |
DAP12 interactions | 40 | 6.59e-01 | 4.03e-02 | 8.78e-01 |
RUNX2 regulates bone development | 31 | 6.98e-01 | -4.02e-02 | 8.90e-01 |
tRNA modification in the nucleus and cytosol | 43 | 6.48e-01 | 4.02e-02 | 8.75e-01 |
Defective B3GALTL causes PpS | 38 | 6.69e-01 | -4.01e-02 | 8.82e-01 |
Metal ion SLC transporters | 24 | 7.35e-01 | -4.00e-02 | 9.05e-01 |
DSCAM interactions | 11 | 8.19e-01 | 3.98e-02 | 9.46e-01 |
Androgen biosynthesis | 11 | 8.20e-01 | 3.97e-02 | 9.46e-01 |
Vitamin D (calciferol) metabolism | 12 | 8.12e-01 | -3.96e-02 | 9.41e-01 |
Ion homeostasis | 54 | 6.16e-01 | -3.94e-02 | 8.63e-01 |
Signaling by TGFB family members | 124 | 4.49e-01 | -3.94e-02 | 7.86e-01 |
NOTCH2 intracellular domain regulates transcription | 12 | 8.14e-01 | 3.93e-02 | 9.42e-01 |
CS/DS degradation | 14 | 8.01e-01 | -3.90e-02 | 9.38e-01 |
Regulation of PTEN gene transcription | 61 | 5.99e-01 | -3.89e-02 | 8.57e-01 |
Cytoprotection by HMOX1 | 60 | 6.02e-01 | -3.89e-02 | 8.59e-01 |
PIP3 activates AKT signaling | 287 | 2.58e-01 | -3.88e-02 | 6.51e-01 |
Centrosome maturation | 81 | 5.48e-01 | -3.86e-02 | 8.30e-01 |
Recruitment of mitotic centrosome proteins and complexes | 81 | 5.48e-01 | -3.86e-02 | 8.30e-01 |
Nuclear Receptor transcription pathway | 53 | 6.28e-01 | -3.85e-02 | 8.67e-01 |
Disorders of transmembrane transporters | 177 | 3.79e-01 | 3.83e-02 | 7.48e-01 |
Mitochondrial tRNA aminoacylation | 20 | 7.68e-01 | 3.82e-02 | 9.21e-01 |
Attachment and Entry 9694614 | 19 | 7.73e-01 | -3.81e-02 | 9.23e-01 |
IRAK1 recruits IKK complex | 14 | 8.05e-01 | -3.81e-02 | 9.39e-01 |
IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | 14 | 8.05e-01 | -3.81e-02 | 9.39e-01 |
FOXO-mediated transcription | 66 | 5.93e-01 | -3.80e-02 | 8.56e-01 |
RNA polymerase II transcribes snRNA genes | 74 | 5.72e-01 | 3.80e-02 | 8.46e-01 |
Maturation of spike protein 9683686 | 5 | 8.83e-01 | 3.80e-02 | 9.76e-01 |
Transcriptional regulation by RUNX3 | 95 | 5.23e-01 | 3.79e-02 | 8.18e-01 |
Creation of C4 and C2 activators | 14 | 8.06e-01 | -3.79e-02 | 9.39e-01 |
Signaling by TGF-beta Receptor Complex | 94 | 5.28e-01 | -3.77e-02 | 8.20e-01 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 17 | 7.89e-01 | 3.74e-02 | 9.34e-01 |
Processing of Intronless Pre-mRNAs | 20 | 7.72e-01 | 3.74e-02 | 9.22e-01 |
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 32 | 7.15e-01 | 3.73e-02 | 8.99e-01 |
Regulation of Glucokinase by Glucokinase Regulatory Protein | 32 | 7.15e-01 | 3.73e-02 | 8.99e-01 |
Base-Excision Repair, AP Site Formation | 40 | 6.85e-01 | -3.70e-02 | 8.86e-01 |
G alpha (q) signalling events | 216 | 3.48e-01 | -3.70e-02 | 7.17e-01 |
Nectin/Necl trans heterodimerization | 7 | 8.66e-01 | 3.69e-02 | 9.68e-01 |
Nef and signal transduction | 8 | 8.58e-01 | -3.66e-02 | 9.68e-01 |
Disease | 1765 | 1.06e-02 | -3.65e-02 | 1.93e-01 |
Downstream signaling of activated FGFR2 | 30 | 7.30e-01 | -3.65e-02 | 9.01e-01 |
PCP/CE pathway | 92 | 5.46e-01 | 3.64e-02 | 8.30e-01 |
Diseases associated with N-glycosylation of proteins | 20 | 7.78e-01 | 3.64e-02 | 9.26e-01 |
Phospholipase C-mediated cascade; FGFR3 | 13 | 8.21e-01 | -3.62e-02 | 9.47e-01 |
Cellular response to chemical stress | 213 | 3.64e-01 | -3.61e-02 | 7.35e-01 |
HSF1 activation | 29 | 7.37e-01 | -3.61e-02 | 9.05e-01 |
COPI-independent Golgi-to-ER retrograde traffic | 51 | 6.56e-01 | -3.61e-02 | 8.76e-01 |
TP53 Regulates Transcription of Cell Cycle Genes | 48 | 6.67e-01 | 3.59e-02 | 8.81e-01 |
FCERI mediated MAPK activation | 32 | 7.27e-01 | 3.57e-02 | 9.00e-01 |
Binding and Uptake of Ligands by Scavenger Receptors | 41 | 6.93e-01 | 3.56e-02 | 8.90e-01 |
Toll Like Receptor 4 (TLR4) Cascade | 144 | 4.62e-01 | -3.55e-02 | 7.94e-01 |
FGFR1 ligand binding and activation | 18 | 7.94e-01 | 3.55e-02 | 9.35e-01 |
RNA Polymerase II Pre-transcription Events | 80 | 5.84e-01 | 3.54e-02 | 8.49e-01 |
Cardiogenesis | 27 | 7.50e-01 | -3.54e-02 | 9.14e-01 |
Assembly Of The HIV Virion | 16 | 8.06e-01 | -3.54e-02 | 9.39e-01 |
Synthesis of Lipoxins (LX) | 6 | 8.81e-01 | -3.54e-02 | 9.76e-01 |
Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | 18 | 7.96e-01 | 3.52e-02 | 9.36e-01 |
activated TAK1 mediates p38 MAPK activation | 23 | 7.71e-01 | 3.50e-02 | 9.22e-01 |
Cell Cycle | 648 | 1.29e-01 | 3.49e-02 | 5.13e-01 |
Autophagy | 148 | 4.66e-01 | -3.47e-02 | 7.95e-01 |
Free fatty acids regulate insulin secretion | 11 | 8.42e-01 | -3.47e-02 | 9.60e-01 |
SUMOylation of RNA binding proteins | 47 | 6.81e-01 | -3.46e-02 | 8.86e-01 |
Translation of Structural Proteins 9694635 | 57 | 6.51e-01 | 3.46e-02 | 8.75e-01 |
Role of phospholipids in phagocytosis | 25 | 7.65e-01 | -3.45e-02 | 9.20e-01 |
Synthesis of diphthamide-EEF2 | 8 | 8.66e-01 | -3.43e-02 | 9.68e-01 |
Maturation of spike protein 9694548 | 37 | 7.18e-01 | 3.43e-02 | 8.99e-01 |
Cell Cycle, Mitotic | 520 | 1.82e-01 | 3.42e-02 | 5.96e-01 |
Metabolism of RNA | 721 | 1.19e-01 | 3.40e-02 | 5.00e-01 |
Chaperone Mediated Autophagy | 22 | 7.82e-01 | 3.40e-02 | 9.30e-01 |
Na+/Cl- dependent neurotransmitter transporters | 19 | 7.98e-01 | -3.39e-02 | 9.36e-01 |
Mitochondrial translation | 93 | 5.74e-01 | 3.37e-02 | 8.47e-01 |
Activation of NMDA receptors and postsynaptic events | 92 | 5.77e-01 | 3.37e-02 | 8.48e-01 |
Activation of RAC1 | 13 | 8.34e-01 | -3.36e-02 | 9.55e-01 |
Integrin cell surface interactions | 85 | 5.96e-01 | -3.33e-02 | 8.57e-01 |
Inositol phosphate metabolism | 48 | 6.91e-01 | -3.32e-02 | 8.89e-01 |
Regulation of PLK1 Activity at G2/M Transition | 87 | 5.93e-01 | -3.32e-02 | 8.56e-01 |
Cyclin D associated events in G1 | 46 | 6.97e-01 | 3.31e-02 | 8.90e-01 |
G1 Phase | 46 | 6.97e-01 | 3.31e-02 | 8.90e-01 |
Transcriptional regulation by RUNX1 | 208 | 4.10e-01 | -3.31e-02 | 7.67e-01 |
Interleukin-4 and Interleukin-13 signaling | 108 | 5.52e-01 | 3.31e-02 | 8.30e-01 |
SARS-CoV-1-host interactions | 95 | 5.78e-01 | 3.30e-02 | 8.48e-01 |
Export of Viral Ribonucleoproteins from Nucleus | 33 | 7.44e-01 | 3.29e-02 | 9.10e-01 |
Viral Messenger RNA Synthesis | 44 | 7.06e-01 | 3.29e-02 | 8.92e-01 |
HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | 55 | 6.75e-01 | 3.27e-02 | 8.86e-01 |
Nucleotide Excision Repair | 109 | 5.55e-01 | 3.27e-02 | 8.32e-01 |
SARS-CoV-2-host interactions | 196 | 4.31e-01 | 3.26e-02 | 7.77e-01 |
Activation of RAS in B cells | 5 | 9.00e-01 | -3.25e-02 | 9.80e-01 |
Toll-like Receptor Cascades | 166 | 4.70e-01 | -3.25e-02 | 7.95e-01 |
HCMV Early Events | 103 | 5.69e-01 | -3.25e-02 | 8.44e-01 |
Innate Immune System | 1033 | 7.73e-02 | 3.25e-02 | 4.34e-01 |
Zinc transporters | 15 | 8.28e-01 | -3.24e-02 | 9.51e-01 |
MAP3K8 (TPL2)-dependent MAPK1/3 activation | 16 | 8.23e-01 | -3.24e-02 | 9.47e-01 |
FGFR1c ligand binding and activation | 14 | 8.34e-01 | -3.24e-02 | 9.55e-01 |
Activated NOTCH1 Transmits Signal to the Nucleus | 31 | 7.56e-01 | -3.22e-02 | 9.17e-01 |
Creatine metabolism | 10 | 8.60e-01 | 3.22e-02 | 9.68e-01 |
SHC-mediated cascade:FGFR1 | 21 | 7.99e-01 | 3.21e-02 | 9.37e-01 |
Sensory processing of sound by inner hair cells of the cochlea | 67 | 6.51e-01 | -3.20e-02 | 8.75e-01 |
Respiratory syncytial virus (RSV) genome replication, transcription and translation | 16 | 8.25e-01 | 3.18e-02 | 9.50e-01 |
Formation of HIV-1 elongation complex containing HIV-1 Tat | 42 | 7.23e-01 | -3.16e-02 | 8.99e-01 |
HIV Transcription Elongation | 42 | 7.23e-01 | -3.16e-02 | 8.99e-01 |
Tat-mediated elongation of the HIV-1 transcript | 42 | 7.23e-01 | -3.16e-02 | 8.99e-01 |
Glucuronidation | 22 | 7.98e-01 | -3.16e-02 | 9.36e-01 |
Deadenylation of mRNA | 22 | 7.98e-01 | -3.16e-02 | 9.36e-01 |
Metabolism of porphyrins | 28 | 7.73e-01 | 3.15e-02 | 9.22e-01 |
CD209 (DC-SIGN) signaling | 21 | 8.03e-01 | -3.15e-02 | 9.39e-01 |
MAPK1/MAPK3 signaling | 279 | 3.69e-01 | -3.13e-02 | 7.39e-01 |
Transcriptional regulation by small RNAs | 70 | 6.52e-01 | -3.12e-02 | 8.75e-01 |
Degradation of beta-catenin by the destruction complex | 85 | 6.19e-01 | 3.12e-02 | 8.63e-01 |
Signaling by Retinoic Acid | 43 | 7.25e-01 | 3.10e-02 | 9.00e-01 |
Glycogen metabolism | 25 | 7.90e-01 | 3.07e-02 | 9.34e-01 |
Phosphate bond hydrolysis by NUDT proteins | 7 | 8.88e-01 | -3.06e-02 | 9.77e-01 |
Mitochondrial translation elongation | 87 | 6.22e-01 | 3.06e-02 | 8.63e-01 |
ECM proteoglycans | 76 | 6.46e-01 | -3.05e-02 | 8.75e-01 |
Formation of TC-NER Pre-Incision Complex | 52 | 7.04e-01 | 3.04e-02 | 8.91e-01 |
Macroautophagy | 133 | 5.45e-01 | -3.04e-02 | 8.30e-01 |
Transcriptional regulation of granulopoiesis | 53 | 7.02e-01 | -3.03e-02 | 8.91e-01 |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 78 | 6.47e-01 | 3.00e-02 | 8.75e-01 |
Diseases of Base Excision Repair | 5 | 9.08e-01 | -3.00e-02 | 9.81e-01 |
Pyruvate metabolism | 31 | 7.73e-01 | -3.00e-02 | 9.22e-01 |
Deadenylation-dependent mRNA decay | 53 | 7.07e-01 | -2.98e-02 | 8.92e-01 |
SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 11 | 8.65e-01 | 2.96e-02 | 9.68e-01 |
Heme degradation | 16 | 8.38e-01 | 2.95e-02 | 9.57e-01 |
Assembly of the ORC complex at the origin of replication | 32 | 7.74e-01 | -2.93e-02 | 9.23e-01 |
Attenuation phase | 26 | 7.96e-01 | -2.93e-02 | 9.36e-01 |
EGR2 and SOX10-mediated initiation of Schwann cell myelination | 29 | 7.85e-01 | -2.92e-02 | 9.32e-01 |
Activation of AMPK downstream of NMDARs | 27 | 7.93e-01 | 2.92e-02 | 9.35e-01 |
Inwardly rectifying K+ channels | 35 | 7.66e-01 | 2.91e-02 | 9.20e-01 |
Neurexins and neuroligins | 57 | 7.05e-01 | 2.90e-02 | 8.91e-01 |
RNA Polymerase III Transcription Initiation | 36 | 7.64e-01 | -2.90e-02 | 9.20e-01 |
MET activates RAS signaling | 11 | 8.68e-01 | -2.90e-02 | 9.68e-01 |
Gap-filling DNA repair synthesis and ligation in TC-NER | 63 | 6.91e-01 | 2.89e-02 | 8.89e-01 |
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 35 | 7.68e-01 | -2.88e-02 | 9.21e-01 |
Regulation of HMOX1 expression and activity | 5 | 9.11e-01 | 2.88e-02 | 9.81e-01 |
Interleukin-37 signaling | 21 | 8.20e-01 | -2.87e-02 | 9.46e-01 |
Signaling by NOTCH4 | 82 | 6.55e-01 | 2.85e-02 | 8.76e-01 |
M Phase | 377 | 3.43e-01 | 2.84e-02 | 7.12e-01 |
Negative regulators of DDX58/IFIH1 signaling | 35 | 7.71e-01 | 2.84e-02 | 9.22e-01 |
RAF/MAP kinase cascade | 273 | 4.21e-01 | -2.83e-02 | 7.69e-01 |
Axonal growth inhibition (RHOA activation) | 9 | 8.83e-01 | -2.83e-02 | 9.76e-01 |
RNA Polymerase III Transcription Initiation From Type 1 Promoter | 28 | 7.98e-01 | -2.80e-02 | 9.36e-01 |
Pentose phosphate pathway | 15 | 8.53e-01 | 2.77e-02 | 9.65e-01 |
Hemostasis | 592 | 2.50e-01 | -2.76e-02 | 6.47e-01 |
LGI-ADAM interactions | 14 | 8.59e-01 | 2.75e-02 | 9.68e-01 |
Generic Transcription Pathway | 1221 | 1.10e-01 | 2.71e-02 | 4.93e-01 |
Lipophagy | 9 | 8.88e-01 | -2.70e-02 | 9.77e-01 |
ERK/MAPK targets | 22 | 8.26e-01 | -2.70e-02 | 9.50e-01 |
Scavenging of heme from plasma | 12 | 8.72e-01 | -2.68e-02 | 9.70e-01 |
rRNA processing in the mitochondrion | 10 | 8.83e-01 | 2.68e-02 | 9.76e-01 |
Metabolism of cofactors | 19 | 8.40e-01 | 2.68e-02 | 9.59e-01 |
Mitotic Prometaphase | 200 | 5.16e-01 | 2.67e-02 | 8.15e-01 |
FCGR3A-mediated IL10 synthesis | 38 | 7.77e-01 | -2.65e-02 | 9.26e-01 |
Transcriptional Regulation by NPAS4 | 33 | 7.92e-01 | -2.65e-02 | 9.35e-01 |
Membrane binding and targetting of GAG proteins | 14 | 8.66e-01 | -2.61e-02 | 9.68e-01 |
Synthesis And Processing Of GAG, GAGPOL Polyproteins | 14 | 8.66e-01 | -2.61e-02 | 9.68e-01 |
Recruitment of NuMA to mitotic centrosomes | 93 | 6.65e-01 | -2.60e-02 | 8.80e-01 |
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 93 | 6.66e-01 | 2.59e-02 | 8.81e-01 |
Amplification of signal from the kinetochores | 93 | 6.66e-01 | 2.59e-02 | 8.81e-01 |
Processing of Capped Intronless Pre-mRNA | 29 | 8.11e-01 | 2.57e-02 | 9.40e-01 |
p75NTR recruits signalling complexes | 13 | 8.73e-01 | 2.56e-02 | 9.70e-01 |
O-linked glycosylation | 112 | 6.40e-01 | -2.55e-02 | 8.75e-01 |
Recycling pathway of L1 | 47 | 7.63e-01 | 2.55e-02 | 9.20e-01 |
Phospholipase C-mediated cascade; FGFR4 | 15 | 8.65e-01 | -2.54e-02 | 9.68e-01 |
DNA Double-Strand Break Repair | 145 | 5.99e-01 | -2.53e-02 | 8.57e-01 |
RNA Polymerase II Transcription | 1344 | 1.22e-01 | 2.51e-02 | 5.02e-01 |
Sphingolipid de novo biosynthesis | 37 | 7.93e-01 | 2.49e-02 | 9.35e-01 |
Post-translational protein modification | 1401 | 1.19e-01 | -2.48e-02 | 5.00e-01 |
SLBP independent Processing of Histone Pre-mRNAs | 10 | 8.92e-01 | 2.47e-02 | 9.77e-01 |
RUNX2 regulates genes involved in cell migration | 8 | 9.04e-01 | -2.47e-02 | 9.80e-01 |
L1CAM interactions | 119 | 6.44e-01 | 2.45e-02 | 8.75e-01 |
Metabolic disorders of biological oxidation enzymes | 34 | 8.05e-01 | 2.45e-02 | 9.39e-01 |
Sialic acid metabolism | 33 | 8.09e-01 | -2.43e-02 | 9.40e-01 |
Nuclear events mediated by NFE2L2 | 96 | 6.83e-01 | 2.41e-02 | 8.86e-01 |
Glycoprotein hormones | 9 | 9.00e-01 | 2.41e-02 | 9.80e-01 |
Infectious disease | 974 | 2.03e-01 | -2.41e-02 | 6.08e-01 |
Late SARS-CoV-2 Infection Events | 70 | 7.29e-01 | 2.40e-02 | 9.00e-01 |
Iron uptake and transport | 58 | 7.52e-01 | 2.40e-02 | 9.15e-01 |
ATF6 (ATF6-alpha) activates chaperones | 12 | 8.86e-01 | -2.39e-02 | 9.77e-01 |
Transcriptional Regulation by MECP2 | 63 | 7.44e-01 | 2.38e-02 | 9.10e-01 |
Cellular Senescence | 161 | 6.03e-01 | -2.37e-02 | 8.59e-01 |
trans-Golgi Network Vesicle Budding | 71 | 7.30e-01 | -2.37e-02 | 9.01e-01 |
Negative regulation of MET activity | 21 | 8.52e-01 | -2.36e-02 | 9.65e-01 |
PI-3K cascade:FGFR1 | 21 | 8.52e-01 | -2.35e-02 | 9.65e-01 |
Metabolism of amino acids and derivatives | 367 | 4.41e-01 | 2.34e-02 | 7.80e-01 |
Nuclear Pore Complex (NPC) Disassembly | 36 | 8.08e-01 | 2.34e-02 | 9.40e-01 |
SARS-CoV Infections | 406 | 4.19e-01 | -2.34e-02 | 7.69e-01 |
EML4 and NUDC in mitotic spindle formation | 114 | 6.68e-01 | 2.32e-02 | 8.82e-01 |
Acyl chain remodeling of CL | 5 | 9.29e-01 | -2.31e-02 | 9.86e-01 |
Urea cycle | 10 | 9.01e-01 | 2.28e-02 | 9.80e-01 |
Cellular responses to stimuli | 781 | 2.79e-01 | -2.28e-02 | 6.74e-01 |
Induction of Cell-Cell Fusion | 13 | 8.88e-01 | -2.25e-02 | 9.77e-01 |
DNA Damage/Telomere Stress Induced Senescence | 57 | 7.69e-01 | -2.25e-02 | 9.21e-01 |
Kinesins | 60 | 7.63e-01 | -2.25e-02 | 9.20e-01 |
Phase II - Conjugation of compounds | 104 | 6.92e-01 | 2.24e-02 | 8.89e-01 |
Signaling by RNF43 mutants | 8 | 9.12e-01 | 2.24e-02 | 9.81e-01 |
Defects in vitamin and cofactor metabolism | 21 | 8.60e-01 | 2.23e-02 | 9.68e-01 |
Regulation of IFNG signaling | 14 | 8.85e-01 | 2.23e-02 | 9.77e-01 |
SUMOylation of DNA damage response and repair proteins | 77 | 7.35e-01 | -2.23e-02 | 9.05e-01 |
Meiotic recombination | 50 | 7.86e-01 | 2.22e-02 | 9.32e-01 |
Neddylation | 242 | 5.54e-01 | 2.21e-02 | 8.32e-01 |
Cytokine Signaling in Immune system | 751 | 3.09e-01 | -2.18e-02 | 6.97e-01 |
CRMPs in Sema3A signaling | 16 | 8.81e-01 | -2.17e-02 | 9.76e-01 |
Synthesis of IP2, IP, and Ins in the cytosol | 14 | 8.91e-01 | -2.12e-02 | 9.77e-01 |
Cellular responses to stress | 767 | 3.19e-01 | -2.11e-02 | 7.03e-01 |
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) | 8 | 9.18e-01 | -2.10e-02 | 9.81e-01 |
G alpha (s) signalling events | 156 | 6.52e-01 | 2.09e-02 | 8.75e-01 |
Gene expression (Transcription) | 1512 | 1.83e-01 | 2.04e-02 | 5.98e-01 |
Transcriptional Regulation by TP53 | 359 | 5.06e-01 | -2.04e-02 | 8.13e-01 |
Signal regulatory protein family interactions | 15 | 8.91e-01 | -2.04e-02 | 9.77e-01 |
Interaction With Cumulus Cells And The Zona Pellucida | 11 | 9.08e-01 | -2.02e-02 | 9.81e-01 |
Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 77 | 7.60e-01 | 2.01e-02 | 9.19e-01 |
Synthesis of Dolichyl-phosphate | 6 | 9.32e-01 | -2.01e-02 | 9.86e-01 |
COPI-mediated anterograde transport | 100 | 7.30e-01 | -2.00e-02 | 9.01e-01 |
KEAP1-NFE2L2 pathway | 129 | 6.95e-01 | -2.00e-02 | 8.90e-01 |
TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | 12 | 9.05e-01 | 1.99e-02 | 9.81e-01 |
Developmental Biology | 1238 | 2.40e-01 | 1.98e-02 | 6.39e-01 |
Formation of the Early Elongation Complex | 32 | 8.47e-01 | -1.96e-02 | 9.65e-01 |
Formation of the HIV-1 Early Elongation Complex | 32 | 8.47e-01 | -1.96e-02 | 9.65e-01 |
RNA Polymerase I Promoter Escape | 53 | 8.05e-01 | 1.96e-02 | 9.39e-01 |
Postmitotic nuclear pore complex (NPC) reformation | 27 | 8.60e-01 | 1.96e-02 | 9.68e-01 |
Maturation of hRSV A proteins | 13 | 9.04e-01 | 1.93e-02 | 9.80e-01 |
TCF dependent signaling in response to WNT | 196 | 6.43e-01 | -1.92e-02 | 8.75e-01 |
Thyroxine biosynthesis | 10 | 9.16e-01 | -1.91e-02 | 9.81e-01 |
MAPK family signaling cascades | 321 | 5.57e-01 | -1.91e-02 | 8.33e-01 |
Activation of SMO | 18 | 8.90e-01 | -1.89e-02 | 9.77e-01 |
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 17 | 8.93e-01 | 1.89e-02 | 9.77e-01 |
Presynaptic function of Kainate receptors | 21 | 8.82e-01 | -1.88e-02 | 9.76e-01 |
Signaling by activated point mutants of FGFR1 | 11 | 9.14e-01 | -1.87e-02 | 9.81e-01 |
Activation of G protein gated Potassium channels | 29 | 8.62e-01 | -1.87e-02 | 9.68e-01 |
G protein gated Potassium channels | 29 | 8.62e-01 | -1.87e-02 | 9.68e-01 |
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 29 | 8.62e-01 | -1.87e-02 | 9.68e-01 |
Negative regulation of FGFR1 signaling | 33 | 8.53e-01 | -1.86e-02 | 9.65e-01 |
Defective factor IX causes hemophilia B | 9 | 9.23e-01 | 1.86e-02 | 9.83e-01 |
Presynaptic depolarization and calcium channel opening | 12 | 9.12e-01 | -1.84e-02 | 9.81e-01 |
mRNA 3’-end processing | 58 | 8.09e-01 | 1.83e-02 | 9.40e-01 |
Negative regulation of FGFR2 signaling | 34 | 8.54e-01 | -1.82e-02 | 9.65e-01 |
Citric acid cycle (TCA cycle) | 22 | 8.82e-01 | -1.82e-02 | 9.76e-01 |
Dissolution of Fibrin Clot | 13 | 9.10e-01 | -1.82e-02 | 9.81e-01 |
PTK6 promotes HIF1A stabilization | 7 | 9.34e-01 | -1.81e-02 | 9.86e-01 |
Small interfering RNA (siRNA) biogenesis | 9 | 9.26e-01 | 1.80e-02 | 9.84e-01 |
FGFR4 ligand binding and activation | 14 | 9.08e-01 | 1.79e-02 | 9.81e-01 |
Signaling by ALK | 28 | 8.70e-01 | -1.79e-02 | 9.69e-01 |
Activated NTRK2 signals through FRS2 and FRS3 | 11 | 9.19e-01 | 1.78e-02 | 9.81e-01 |
Regulation of HSF1-mediated heat shock response | 81 | 7.82e-01 | 1.78e-02 | 9.30e-01 |
Defective B3GALT6 causes EDSP2 and SEMDJL1 | 20 | 8.91e-01 | -1.77e-02 | 9.77e-01 |
Pyrimidine catabolism | 12 | 9.15e-01 | 1.77e-02 | 9.81e-01 |
Signaling by NTRK1 (TRKA) | 115 | 7.43e-01 | -1.77e-02 | 9.10e-01 |
Transport of Ribonucleoproteins into the Host Nucleus | 32 | 8.64e-01 | 1.76e-02 | 9.68e-01 |
NoRC negatively regulates rRNA expression | 68 | 8.03e-01 | -1.75e-02 | 9.39e-01 |
Organelle biogenesis and maintenance | 285 | 6.11e-01 | -1.75e-02 | 8.63e-01 |
Constitutive Signaling by Overexpressed ERBB2 | 11 | 9.21e-01 | -1.73e-02 | 9.83e-01 |
Amino acids regulate mTORC1 | 52 | 8.30e-01 | 1.73e-02 | 9.52e-01 |
RHO GTPases activate IQGAPs | 30 | 8.70e-01 | -1.72e-02 | 9.69e-01 |
CD28 dependent Vav1 pathway | 12 | 9.19e-01 | -1.70e-02 | 9.81e-01 |
HIV Infection | 229 | 6.60e-01 | 1.69e-02 | 8.78e-01 |
Glucagon-type ligand receptors | 32 | 8.70e-01 | -1.67e-02 | 9.69e-01 |
Initiation of Nuclear Envelope (NE) Reformation | 19 | 9.01e-01 | -1.65e-02 | 9.80e-01 |
G alpha (i) signalling events | 313 | 6.20e-01 | 1.63e-02 | 8.63e-01 |
EPHB-mediated forward signaling | 42 | 8.56e-01 | 1.62e-02 | 9.66e-01 |
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 30 | 8.79e-01 | 1.60e-02 | 9.76e-01 |
Activation of NIMA Kinases NEK9, NEK6, NEK7 | 7 | 9.42e-01 | -1.60e-02 | 9.88e-01 |
PI5P Regulates TP53 Acetylation | 8 | 9.38e-01 | -1.59e-02 | 9.87e-01 |
Phospholipase C-mediated cascade: FGFR1 | 16 | 9.12e-01 | 1.59e-02 | 9.81e-01 |
Processing of DNA double-strand break ends | 76 | 8.11e-01 | 1.59e-02 | 9.40e-01 |
RNA Polymerase II Transcription Termination | 67 | 8.23e-01 | 1.58e-02 | 9.47e-01 |
Post-chaperonin tubulin folding pathway | 22 | 8.99e-01 | 1.57e-02 | 9.80e-01 |
Platelet degranulation | 126 | 7.63e-01 | -1.56e-02 | 9.20e-01 |
Platelet calcium homeostasis | 28 | 8.87e-01 | 1.56e-02 | 9.77e-01 |
Sensory processing of sound | 75 | 8.17e-01 | -1.55e-02 | 9.45e-01 |
MTOR signalling | 41 | 8.67e-01 | -1.52e-02 | 9.68e-01 |
Adaptive Immune System | 755 | 4.78e-01 | 1.52e-02 | 8.00e-01 |
MET activates RAP1 and RAC1 | 11 | 9.31e-01 | 1.51e-02 | 9.86e-01 |
Metabolism of non-coding RNA | 53 | 8.53e-01 | -1.47e-02 | 9.65e-01 |
snRNP Assembly | 53 | 8.53e-01 | -1.47e-02 | 9.65e-01 |
Branched-chain amino acid catabolism | 21 | 9.08e-01 | -1.46e-02 | 9.81e-01 |
Myogenesis | 29 | 8.92e-01 | -1.45e-02 | 9.77e-01 |
FRS-mediated FGFR2 signaling | 25 | 9.01e-01 | -1.44e-02 | 9.80e-01 |
Nuclear Envelope (NE) Reassembly | 74 | 8.30e-01 | -1.44e-02 | 9.52e-01 |
Interleukin-35 Signalling | 12 | 9.31e-01 | -1.44e-02 | 9.86e-01 |
Multifunctional anion exchangers | 9 | 9.41e-01 | -1.43e-02 | 9.88e-01 |
TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling | 13 | 9.31e-01 | 1.39e-02 | 9.86e-01 |
Signaling by GPCR | 699 | 5.34e-01 | 1.38e-02 | 8.21e-01 |
Protein localization | 161 | 7.65e-01 | -1.36e-02 | 9.20e-01 |
Synthesis of PIPs at the early endosome membrane | 16 | 9.25e-01 | 1.36e-02 | 9.84e-01 |
Transferrin endocytosis and recycling | 30 | 8.98e-01 | -1.35e-02 | 9.80e-01 |
MASTL Facilitates Mitotic Progression | 10 | 9.41e-01 | -1.34e-02 | 9.88e-01 |
FGFR3 mutant receptor activation | 12 | 9.36e-01 | 1.34e-02 | 9.86e-01 |
Signaling by activated point mutants of FGFR3 | 12 | 9.36e-01 | 1.34e-02 | 9.86e-01 |
DDX58/IFIH1-mediated induction of interferon-alpha/beta | 76 | 8.42e-01 | 1.32e-02 | 9.60e-01 |
Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 12 | 9.37e-01 | -1.32e-02 | 9.87e-01 |
Ion channel transport | 183 | 7.60e-01 | 1.31e-02 | 9.19e-01 |
SUMOylation of intracellular receptors | 30 | 9.02e-01 | -1.29e-02 | 9.80e-01 |
PTK6 Regulates Cell Cycle | 6 | 9.56e-01 | 1.29e-02 | 9.94e-01 |
Negative epigenetic regulation of rRNA expression | 71 | 8.51e-01 | -1.29e-02 | 9.65e-01 |
Asparagine N-linked glycosylation | 303 | 7.00e-01 | -1.29e-02 | 8.90e-01 |
Signaling by NTRK2 (TRKB) | 25 | 9.11e-01 | 1.29e-02 | 9.81e-01 |
Metabolism of nitric oxide: NOS3 activation and regulation | 14 | 9.34e-01 | -1.28e-02 | 9.86e-01 |
Protein-protein interactions at synapses | 88 | 8.38e-01 | 1.26e-02 | 9.57e-01 |
Transport of the SLBP Dependant Mature mRNA | 36 | 8.96e-01 | 1.26e-02 | 9.79e-01 |
Cellular response to heat stress | 99 | 8.29e-01 | -1.25e-02 | 9.52e-01 |
Class I MHC mediated antigen processing & presentation | 378 | 6.77e-01 | -1.25e-02 | 8.86e-01 |
Intraflagellar transport | 51 | 8.78e-01 | 1.24e-02 | 9.75e-01 |
mRNA Editing | 10 | 9.46e-01 | 1.23e-02 | 9.89e-01 |
Signaling by FGFR2 in disease | 43 | 8.89e-01 | -1.23e-02 | 9.77e-01 |
SARS-CoV-2 Infection | 291 | 7.20e-01 | 1.22e-02 | 8.99e-01 |
VxPx cargo-targeting to cilium | 21 | 9.23e-01 | 1.22e-02 | 9.83e-01 |
Regulation of TP53 Activity through Methylation | 19 | 9.27e-01 | 1.21e-02 | 9.85e-01 |
FLT3 signaling through SRC family kinases | 6 | 9.59e-01 | 1.20e-02 | 9.97e-01 |
Transcriptional regulation of white adipocyte differentiation | 84 | 8.51e-01 | 1.19e-02 | 9.65e-01 |
Sodium-coupled sulphate, di- and tri-carboxylate transporters | 5 | 9.64e-01 | -1.18e-02 | 9.97e-01 |
Fanconi Anemia Pathway | 35 | 9.04e-01 | 1.17e-02 | 9.80e-01 |
Interleukin-1 signaling | 114 | 8.29e-01 | -1.17e-02 | 9.52e-01 |
G2/M DNA damage checkpoint | 73 | 8.64e-01 | 1.16e-02 | 9.68e-01 |
MicroRNA (miRNA) biogenesis | 26 | 9.19e-01 | -1.15e-02 | 9.81e-01 |
Complex I biogenesis | 51 | 8.89e-01 | -1.13e-02 | 9.77e-01 |
GDP-fucose biosynthesis | 6 | 9.63e-01 | 1.10e-02 | 9.97e-01 |
MAP kinase activation | 63 | 8.82e-01 | 1.08e-02 | 9.76e-01 |
Scavenging by Class A Receptors | 19 | 9.36e-01 | 1.07e-02 | 9.86e-01 |
Transport of the SLBP independent Mature mRNA | 35 | 9.13e-01 | 1.07e-02 | 9.81e-01 |
Nephrin family interactions | 22 | 9.32e-01 | -1.06e-02 | 9.86e-01 |
Golgi Associated Vesicle Biogenesis | 55 | 8.92e-01 | -1.05e-02 | 9.77e-01 |
RNA Polymerase III Chain Elongation | 18 | 9.40e-01 | 1.02e-02 | 9.88e-01 |
MET receptor recycling | 10 | 9.56e-01 | -1.01e-02 | 9.94e-01 |
RHO GTPases Activate NADPH Oxidases | 24 | 9.32e-01 | -1.00e-02 | 9.86e-01 |
HDR through MMEJ (alt-NHEJ) | 12 | 9.52e-01 | 1.00e-02 | 9.93e-01 |
Maternal to zygotic transition (MZT) | 97 | 8.66e-01 | -9.92e-03 | 9.68e-01 |
Glycogen storage diseases | 16 | 9.45e-01 | 9.90e-03 | 9.89e-01 |
SUMOylation of chromatin organization proteins | 57 | 8.98e-01 | 9.84e-03 | 9.80e-01 |
Gap junction assembly | 36 | 9.19e-01 | -9.79e-03 | 9.81e-01 |
IKK complex recruitment mediated by RIP1 | 23 | 9.35e-01 | -9.76e-03 | 9.86e-01 |
mRNA Splicing | 213 | 8.09e-01 | 9.60e-03 | 9.40e-01 |
Physiological factors | 14 | 9.50e-01 | -9.59e-03 | 9.93e-01 |
Activation of the TFAP2 (AP-2) family of transcription factors | 12 | 9.55e-01 | 9.47e-03 | 9.94e-01 |
Homology Directed Repair | 115 | 8.62e-01 | 9.40e-03 | 9.68e-01 |
SUMOylation of DNA replication proteins | 46 | 9.13e-01 | -9.30e-03 | 9.81e-01 |
Processing of Capped Intron-Containing Pre-mRNA | 282 | 7.88e-01 | 9.29e-03 | 9.33e-01 |
SUMOylation of SUMOylation proteins | 35 | 9.24e-01 | 9.26e-03 | 9.84e-01 |
Aggrephagy | 41 | 9.19e-01 | 9.16e-03 | 9.81e-01 |
Platelet Adhesion to exposed collagen | 16 | 9.49e-01 | 9.15e-03 | 9.92e-01 |
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 109 | 8.70e-01 | 9.09e-03 | 9.69e-01 |
Carboxyterminal post-translational modifications of tubulin | 43 | 9.19e-01 | 8.97e-03 | 9.81e-01 |
Transport of Mature mRNAs Derived from Intronless Transcripts | 43 | 9.19e-01 | 8.91e-03 | 9.81e-01 |
RSK activation | 7 | 9.68e-01 | -8.80e-03 | 9.98e-01 |
Nervous system development | 577 | 7.18e-01 | -8.80e-03 | 8.99e-01 |
Translocation of SLC2A4 (GLUT4) to the plasma membrane | 70 | 9.03e-01 | 8.40e-03 | 9.80e-01 |
Oncogene Induced Senescence | 35 | 9.32e-01 | -8.34e-03 | 9.86e-01 |
Interleukin-17 signaling | 71 | 9.06e-01 | 8.09e-03 | 9.81e-01 |
Factors involved in megakaryocyte development and platelet production | 149 | 8.68e-01 | -7.91e-03 | 9.68e-01 |
Ub-specific processing proteases | 187 | 8.53e-01 | -7.83e-03 | 9.65e-01 |
RUNX3 regulates p14-ARF | 10 | 9.67e-01 | 7.62e-03 | 9.98e-01 |
Beta-catenin independent WNT signaling | 146 | 8.74e-01 | -7.58e-03 | 9.71e-01 |
RUNX1 regulates estrogen receptor mediated transcription | 6 | 9.75e-01 | -7.48e-03 | 9.98e-01 |
alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 13 | 9.63e-01 | 7.48e-03 | 9.97e-01 |
alpha-linolenic acid (ALA) metabolism | 13 | 9.63e-01 | 7.48e-03 | 9.97e-01 |
Metabolism of proteins | 1979 | 5.82e-01 | -7.47e-03 | 8.49e-01 |
Response to elevated platelet cytosolic Ca2+ | 131 | 8.86e-01 | -7.25e-03 | 9.77e-01 |
Transport of Mature mRNA Derived from an Intronless Transcript | 42 | 9.35e-01 | 7.24e-03 | 9.86e-01 |
NOD1/2 Signaling Pathway | 36 | 9.40e-01 | 7.23e-03 | 9.88e-01 |
Axon guidance | 551 | 7.72e-01 | -7.22e-03 | 9.22e-01 |
Beta oxidation of octanoyl-CoA to hexanoyl-CoA | 5 | 9.79e-01 | -6.92e-03 | 9.98e-01 |
Senescence-Associated Secretory Phenotype (SASP) | 75 | 9.18e-01 | -6.90e-03 | 9.81e-01 |
Immune System | 1984 | 6.12e-01 | 6.88e-03 | 8.63e-01 |
RHOT1 GTPase cycle | 5 | 9.79e-01 | 6.87e-03 | 9.98e-01 |
MET activates PI3K/AKT signaling | 6 | 9.77e-01 | -6.76e-03 | 9.98e-01 |
ISG15 antiviral mechanism | 74 | 9.23e-01 | -6.49e-03 | 9.83e-01 |
PKR-mediated signaling | 73 | 9.24e-01 | -6.44e-03 | 9.84e-01 |
tRNA Aminoacylation | 40 | 9.44e-01 | -6.41e-03 | 9.89e-01 |
Termination of O-glycan biosynthesis | 25 | 9.56e-01 | 6.33e-03 | 9.94e-01 |
Telomere Maintenance | 89 | 9.18e-01 | -6.29e-03 | 9.81e-01 |
Chondroitin sulfate biosynthesis | 20 | 9.62e-01 | -6.23e-03 | 9.97e-01 |
Cell surface interactions at the vascular wall | 131 | 9.02e-01 | -6.22e-03 | 9.80e-01 |
p75NTR regulates axonogenesis | 10 | 9.74e-01 | 6.06e-03 | 9.98e-01 |
Signaling by LRP5 mutants | 6 | 9.81e-01 | -5.75e-03 | 9.98e-01 |
GPCR downstream signalling | 626 | 8.06e-01 | -5.75e-03 | 9.39e-01 |
PI-3K cascade:FGFR2 | 23 | 9.63e-01 | 5.64e-03 | 9.97e-01 |
Rev-mediated nuclear export of HIV RNA | 35 | 9.55e-01 | 5.52e-03 | 9.94e-01 |
Interleukin-12 family signaling | 53 | 9.45e-01 | 5.52e-03 | 9.89e-01 |
mRNA Splicing - Major Pathway | 202 | 8.93e-01 | 5.49e-03 | 9.77e-01 |
STAT3 nuclear events downstream of ALK signaling | 11 | 9.75e-01 | -5.43e-03 | 9.98e-01 |
ROBO receptors bind AKAP5 | 9 | 9.78e-01 | 5.32e-03 | 9.98e-01 |
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 17 | 9.70e-01 | -5.26e-03 | 9.98e-01 |
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 17 | 9.70e-01 | -5.26e-03 | 9.98e-01 |
Post NMDA receptor activation events | 79 | 9.36e-01 | 5.26e-03 | 9.86e-01 |
Cilium Assembly | 196 | 9.02e-01 | -5.08e-03 | 9.80e-01 |
Nephron development | 13 | 9.75e-01 | -5.04e-03 | 9.98e-01 |
PTEN Regulation | 158 | 9.14e-01 | -5.00e-03 | 9.81e-01 |
Interactions of Rev with host cellular proteins | 37 | 9.61e-01 | 4.67e-03 | 9.97e-01 |
Ficolins bind to repetitive carbohydrate structures on the target cell surface | 5 | 9.86e-01 | -4.51e-03 | 9.98e-01 |
Classical antibody-mediated complement activation | 6 | 9.85e-01 | -4.44e-03 | 9.98e-01 |
Synthesis of substrates in N-glycan biosythesis | 63 | 9.51e-01 | -4.43e-03 | 9.93e-01 |
DNA Repair | 302 | 8.96e-01 | -4.38e-03 | 9.79e-01 |
TP53 Regulates Metabolic Genes | 86 | 9.45e-01 | 4.34e-03 | 9.89e-01 |
RUNX2 regulates osteoblast differentiation | 24 | 9.71e-01 | 4.23e-03 | 9.98e-01 |
Sodium/Proton exchangers | 9 | 9.83e-01 | -4.20e-03 | 9.98e-01 |
eNOS activation | 10 | 9.82e-01 | -4.06e-03 | 9.98e-01 |
Neurotransmitter clearance | 10 | 9.83e-01 | -3.83e-03 | 9.98e-01 |
Transport of Mature mRNA derived from an Intron-Containing Transcript | 73 | 9.56e-01 | 3.77e-03 | 9.94e-01 |
SARS-CoV-1 Infection | 140 | 9.42e-01 | 3.58e-03 | 9.88e-01 |
Endogenous sterols | 27 | 9.75e-01 | -3.54e-03 | 9.98e-01 |
Intra-Golgi traffic | 44 | 9.68e-01 | 3.48e-03 | 9.98e-01 |
Signaling by FGFR2 IIIa TM | 19 | 9.80e-01 | -3.34e-03 | 9.98e-01 |
Selective autophagy | 78 | 9.62e-01 | -3.16e-03 | 9.97e-01 |
RNA Polymerase III Transcription Initiation From Type 2 Promoter | 27 | 9.78e-01 | -3.12e-03 | 9.98e-01 |
Late Phase of HIV Life Cycle | 135 | 9.51e-01 | -3.03e-03 | 9.93e-01 |
Neutrophil degranulation | 474 | 9.11e-01 | 2.99e-03 | 9.81e-01 |
NFE2L2 regulating inflammation associated genes | 5 | 9.91e-01 | 2.96e-03 | 9.98e-01 |
Vitamin B2 (riboflavin) metabolism | 7 | 9.89e-01 | -2.92e-03 | 9.98e-01 |
Dopamine receptors | 5 | 9.91e-01 | -2.89e-03 | 9.98e-01 |
SHC-mediated cascade:FGFR3 | 18 | 9.83e-01 | -2.85e-03 | 9.98e-01 |
HIV Life Cycle | 148 | 9.53e-01 | -2.78e-03 | 9.94e-01 |
Synthesis of PIPs at the late endosome membrane | 11 | 9.87e-01 | 2.75e-03 | 9.98e-01 |
Regulation of pyruvate dehydrogenase (PDH) complex | 16 | 9.85e-01 | 2.70e-03 | 9.98e-01 |
Meiosis | 82 | 9.67e-01 | 2.68e-03 | 9.98e-01 |
Acyl chain remodelling of PI | 17 | 9.85e-01 | -2.68e-03 | 9.98e-01 |
Downregulation of TGF-beta receptor signaling | 26 | 9.83e-01 | 2.37e-03 | 9.98e-01 |
Antigen processing: Ubiquitination & Proteasome degradation | 306 | 9.44e-01 | -2.32e-03 | 9.89e-01 |
Signaling by NTRKs | 134 | 9.65e-01 | 2.19e-03 | 9.98e-01 |
Passive transport by Aquaporins | 13 | 9.89e-01 | -2.16e-03 | 9.98e-01 |
Insulin receptor recycling | 29 | 9.84e-01 | -2.10e-03 | 9.98e-01 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 35 | 9.83e-01 | 2.04e-03 | 9.98e-01 |
SHC-mediated cascade:FGFR4 | 20 | 9.88e-01 | 1.91e-03 | 9.98e-01 |
ATF6 (ATF6-alpha) activates chaperone genes | 10 | 9.92e-01 | -1.87e-03 | 9.98e-01 |
RNA Polymerase III Transcription Initiation From Type 3 Promoter | 28 | 9.86e-01 | 1.87e-03 | 9.98e-01 |
Fatty acyl-CoA biosynthesis | 38 | 9.85e-01 | 1.76e-03 | 9.98e-01 |
Signaling by Hedgehog | 149 | 9.71e-01 | 1.74e-03 | 9.98e-01 |
N-glycan antennae elongation in the medial/trans-Golgi | 26 | 9.89e-01 | 1.55e-03 | 9.98e-01 |
Base Excision Repair | 68 | 9.83e-01 | -1.45e-03 | 9.98e-01 |
Synthesis of pyrophosphates in the cytosol | 10 | 9.94e-01 | 1.42e-03 | 9.98e-01 |
Interleukin-1 family signaling | 152 | 9.76e-01 | -1.40e-03 | 9.98e-01 |
Reproduction | 119 | 9.80e-01 | 1.34e-03 | 9.98e-01 |
Formation of HIV elongation complex in the absence of HIV Tat | 44 | 9.90e-01 | -1.13e-03 | 9.98e-01 |
Cellular hexose transport | 22 | 9.93e-01 | -1.11e-03 | 9.98e-01 |
RHOBTB2 GTPase cycle | 23 | 9.93e-01 | -1.11e-03 | 9.98e-01 |
Mitochondrial protein degradation | 87 | 9.86e-01 | -1.09e-03 | 9.98e-01 |
Formation of RNA Pol II elongation complex | 57 | 9.89e-01 | -1.06e-03 | 9.98e-01 |
RNA Polymerase II Transcription Elongation | 57 | 9.89e-01 | -1.06e-03 | 9.98e-01 |
Lysosphingolipid and LPA receptors | 14 | 9.95e-01 | -9.93e-04 | 9.98e-01 |
Cobalamin (Cbl, vitamin B12) transport and metabolism | 21 | 9.94e-01 | -9.46e-04 | 9.98e-01 |
Gene Silencing by RNA | 104 | 9.88e-01 | -8.80e-04 | 9.98e-01 |
RHO GTPases Activate Formins | 137 | 9.87e-01 | -7.90e-04 | 9.98e-01 |
Activation of Matrix Metalloproteinases | 32 | 9.94e-01 | -7.09e-04 | 9.98e-01 |
Transport of Mature Transcript to Cytoplasm | 82 | 9.93e-01 | 5.81e-04 | 9.98e-01 |
Deubiquitination | 261 | 9.88e-01 | 5.60e-04 | 9.98e-01 |
Signaling by Interleukins | 448 | 9.86e-01 | 4.72e-04 | 9.98e-01 |
Early Phase of HIV Life Cycle | 14 | 9.98e-01 | 4.41e-04 | 9.99e-01 |
Signaling by NOTCH2 | 33 | 9.97e-01 | 4.02e-04 | 9.99e-01 |
Sensory processing of sound by outer hair cells of the cochlea | 53 | 9.97e-01 | 2.65e-04 | 9.99e-01 |
Netrin-1 signaling | 49 | 9.98e-01 | -1.70e-04 | 9.99e-01 |
Trafficking and processing of endosomal TLR | 13 | 9.99e-01 | 1.50e-04 | 9.99e-01 |
IRF3-mediated induction of type I IFN | 13 | 9.99e-01 | -1.17e-04 | 9.99e-01 |
Viral Infection Pathways | 786 | 9.98e-01 | 5.18e-05 | 9.99e-01 |
Fatty acids
573 | |
---|---|
set | Fatty acids |
setSize | 15 |
pANOVA | 1.27e-06 |
s.dist | 0.722 |
p.adjustANOVA | 0.00051 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CYP4F2 | 11778 |
CYP2A7 | 11465 |
CYP4B1 | 11439 |
CYP4F8 | 11297 |
CYP2A13 | 11292 |
CYP4F12 | 10773 |
CYP2F1 | 10756 |
CYP4F3 | 10723 |
CYP2B6 | 10584 |
CYP4F22 | 10494 |
CYP4F11 | 10463 |
CYP4A11 | 8201 |
CYP2D6 | 7364 |
CYP4A22 | 1397 |
CYP2J2 | -7969 |
GeneID | Gene Rank |
---|---|
CYP4F2 | 11778 |
CYP2A7 | 11465 |
CYP4B1 | 11439 |
CYP4F8 | 11297 |
CYP2A13 | 11292 |
CYP4F12 | 10773 |
CYP2F1 | 10756 |
CYP4F3 | 10723 |
CYP2B6 | 10584 |
CYP4F22 | 10494 |
CYP4F11 | 10463 |
CYP4A11 | 8201 |
CYP2D6 | 7364 |
CYP4A22 | 1397 |
CYP2J2 | -7969 |
Eicosanoids
499 | |
---|---|
set | Eicosanoids |
setSize | 12 |
pANOVA | 5.25e-05 |
s.dist | 0.674 |
p.adjustANOVA | 0.00704 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CYP4F2 | 11778 |
CYP4B1 | 11439 |
CYP4F8 | 11297 |
CYP4F12 | 10773 |
CYP4F3 | 10723 |
CYP4F22 | 10494 |
CYP4F11 | 10463 |
CYP4A11 | 8201 |
CYP8B1 | 4523 |
TBXAS1 | 4322 |
PTGIS | 1992 |
CYP4A22 | 1397 |
GeneID | Gene Rank |
---|---|
CYP4F2 | 11778 |
CYP4B1 | 11439 |
CYP4F8 | 11297 |
CYP4F12 | 10773 |
CYP4F3 | 10723 |
CYP4F22 | 10494 |
CYP4F11 | 10463 |
CYP4A11 | 8201 |
CYP8B1 | 4523 |
TBXAS1 | 4322 |
PTGIS | 1992 |
CYP4A22 | 1397 |
Amino Acid conjugation
104 | |
---|---|
set | Amino Acid conjugation |
setSize | 9 |
pANOVA | 0.000838 |
s.dist | 0.643 |
p.adjustANOVA | 0.0562 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
ACSM2B | 11530 |
ACSM4 | 11437 |
ACSM1 | 11167 |
ACSM2A | 10922 |
ACSM5 | 10536 |
GLYAT | 9490 |
GLYATL2 | 6889 |
GLYATL3 | -223 |
GLYATL1 | -1926 |
GeneID | Gene Rank |
---|---|
ACSM2B | 11530 |
ACSM4 | 11437 |
ACSM1 | 11167 |
ACSM2A | 10922 |
ACSM5 | 10536 |
GLYAT | 9490 |
GLYATL2 | 6889 |
GLYATL3 | -223 |
GLYATL1 | -1926 |
Conjugation of carboxylic acids
307 | |
---|---|
set | Conjugation of carboxylic acids |
setSize | 9 |
pANOVA | 0.000838 |
s.dist | 0.643 |
p.adjustANOVA | 0.0562 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
ACSM2B | 11530 |
ACSM4 | 11437 |
ACSM1 | 11167 |
ACSM2A | 10922 |
ACSM5 | 10536 |
GLYAT | 9490 |
GLYATL2 | 6889 |
GLYATL3 | -223 |
GLYATL1 | -1926 |
GeneID | Gene Rank |
---|---|
ACSM2B | 11530 |
ACSM4 | 11437 |
ACSM1 | 11167 |
ACSM2A | 10922 |
ACSM5 | 10536 |
GLYAT | 9490 |
GLYATL2 | 6889 |
GLYATL3 | -223 |
GLYATL1 | -1926 |
Conjugation of salicylate with glycine
308 | |
---|---|
set | Conjugation of salicylate with glycine |
setSize | 8 |
pANOVA | 0.003 |
s.dist | 0.606 |
p.adjustANOVA | 0.0974 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
ACSM2B | 11530 |
ACSM4 | 11437 |
ACSM2A | 10922 |
ACSM5 | 10536 |
GLYAT | 9490 |
GLYATL2 | 6889 |
GLYATL3 | -223 |
GLYATL1 | -1926 |
GeneID | Gene Rank |
---|---|
ACSM2B | 11530 |
ACSM4 | 11437 |
ACSM2A | 10922 |
ACSM5 | 10536 |
GLYAT | 9490 |
GLYATL2 | 6889 |
GLYATL3 | -223 |
GLYATL1 | -1926 |
Type I hemidesmosome assembly
1915 | |
---|---|
set | Type I hemidesmosome assembly |
setSize | 11 |
pANOVA | 0.000779 |
s.dist | -0.585 |
p.adjustANOVA | 0.056 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
KRT14 | -10752 |
CD151 | -10355 |
KRT5 | -10178 |
LAMC2 | -9981 |
LAMB3 | -9811 |
ITGB4 | -8918 |
PLEC | -7586 |
COL17A1 | -4278 |
DST | -1462 |
LAMA3 | 1182 |
ITGA6 | 2017 |
GeneID | Gene Rank |
---|---|
KRT14 | -10752 |
CD151 | -10355 |
KRT5 | -10178 |
LAMC2 | -9981 |
LAMB3 | -9811 |
ITGB4 | -8918 |
PLEC | -7586 |
COL17A1 | -4278 |
DST | -1462 |
LAMA3 | 1182 |
ITGA6 | 2017 |
RUNX1 regulates transcription of genes involved in
differentiation of keratinocytes
1372 | |
---|---|
set | RUNX1 regulates transcription of genes involved in differentiation of keratinocytes |
setSize | 8 |
pANOVA | 0.00446 |
s.dist | 0.581 |
p.adjustANOVA | 0.118 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CTSK | 10173 |
CTSV | 9371 |
SERPINB13 | 9044 |
SOCS4 | 8735 |
SOCS3 | 8606 |
CBFB | 8016 |
CTSL | 5264 |
RUNX1 | -2874 |
GeneID | Gene Rank |
---|---|
CTSK | 10173 |
CTSV | 9371 |
SERPINB13 | 9044 |
SOCS4 | 8735 |
SOCS3 | 8606 |
CBFB | 8016 |
CTSL | 5264 |
RUNX1 | -2874 |
ChREBP activates metabolic gene expression
263 | |
---|---|
set | ChREBP activates metabolic gene expression |
setSize | 8 |
pANOVA | 0.00685 |
s.dist | -0.552 |
p.adjustANOVA | 0.155 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
FASN | -9592 |
MLXIPL | -8921 |
AGPAT1 | -7134 |
ACACB | -5352 |
MLX | -5191 |
ACACA | -4970 |
ACLY | -4350 |
PKLR | -2462 |
GeneID | Gene Rank |
---|---|
FASN | -9592 |
MLXIPL | -8921 |
AGPAT1 | -7134 |
ACACB | -5352 |
MLX | -5191 |
ACACA | -4970 |
ACLY | -4350 |
PKLR | -2462 |
Formyl peptide receptors bind formyl peptides and many other
ligands
610 | |
---|---|
set | Formyl peptide receptors bind formyl peptides and many other ligands |
setSize | 8 |
pANOVA | 0.00824 |
s.dist | 0.539 |
p.adjustANOVA | 0.167 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CCL23 | 11295 |
ANXA1 | 11014 |
FPR2 | 10947 |
FPR3 | 10705 |
FPR1 | 10642 |
SAA1 | 1892 |
HEBP1 | -456 |
APP | -3499 |
GeneID | Gene Rank |
---|---|
CCL23 | 11295 |
ANXA1 | 11014 |
FPR2 | 10947 |
FPR3 | 10705 |
FPR1 | 10642 |
SAA1 | 1892 |
HEBP1 | -456 |
APP | -3499 |
CYP2E1 reactions
219 | |
---|---|
set | CYP2E1 reactions |
setSize | 11 |
pANOVA | 0.0022 |
s.dist | 0.533 |
p.adjustANOVA | 0.0974 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CYP2A7 | 11465 |
CYP2C8 | 11395 |
CYP2A13 | 11292 |
CYP2F1 | 10756 |
CYP2B6 | 10584 |
CYP2C19 | 10176 |
CYP2D6 | 7364 |
CYP2A6 | 2709 |
CYP2E1 | 2280 |
CYP2S1 | -3035 |
CYP2C9 | -3558 |
GeneID | Gene Rank |
---|---|
CYP2A7 | 11465 |
CYP2C8 | 11395 |
CYP2A13 | 11292 |
CYP2F1 | 10756 |
CYP2B6 | 10584 |
CYP2C19 | 10176 |
CYP2D6 | 7364 |
CYP2A6 | 2709 |
CYP2E1 | 2280 |
CYP2S1 | -3035 |
CYP2C9 | -3558 |
EGFR interacts with phospholipase C-gamma
479 | |
---|---|
set | EGFR interacts with phospholipase C-gamma |
setSize | 9 |
pANOVA | 0.0064 |
s.dist | -0.525 |
p.adjustANOVA | 0.15 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
EPGN | -10955 |
AREG | -10924 |
EREG | -9691 |
PLCG1 | -6901 |
BTC | -6076 |
EGFR | -3464 |
EGF | -3037 |
HBEGF | -1421 |
TGFA | 1329 |
GeneID | Gene Rank |
---|---|
EPGN | -10955 |
AREG | -10924 |
EREG | -9691 |
PLCG1 | -6901 |
BTC | -6076 |
EGFR | -3464 |
EGF | -3037 |
HBEGF | -1421 |
TGFA | 1329 |
Mucopolysaccharidoses
1001 | |
---|---|
set | Mucopolysaccharidoses |
setSize | 11 |
pANOVA | 0.00269 |
s.dist | -0.523 |
p.adjustANOVA | 0.0974 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
HYAL1 | -10554 |
GALNS | -8972 |
SGSH | -7645 |
IDUA | -7489 |
NAGLU | -7202 |
GUSB | -7065 |
HGSNAT | -5255 |
GLB1 | -5137 |
ARSB | -4376 |
IDS | -842 |
GNS | 2320 |
GeneID | Gene Rank |
---|---|
HYAL1 | -10554 |
GALNS | -8972 |
SGSH | -7645 |
IDUA | -7489 |
NAGLU | -7202 |
GUSB | -7065 |
HGSNAT | -5255 |
GLB1 | -5137 |
ARSB | -4376 |
IDS | -842 |
GNS | 2320 |
Pre-NOTCH Processing in the Endoplasmic Reticulum
1245 | |
---|---|
set | Pre-NOTCH Processing in the Endoplasmic Reticulum |
setSize | 6 |
pANOVA | 0.0271 |
s.dist | -0.521 |
p.adjustANOVA | 0.29 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
NOTCH3 | -8566 |
NOTCH1 | -6878 |
POGLUT1 | -5905 |
NOTCH2 | -4991 |
POFUT1 | -3971 |
NOTCH4 | -3533 |
GeneID | Gene Rank |
---|---|
NOTCH3 | -8566 |
NOTCH1 | -6878 |
POGLUT1 | -5905 |
NOTCH2 | -4991 |
POFUT1 | -3971 |
NOTCH4 | -3533 |
Transport of fatty acids
1898 | |
---|---|
set | Transport of fatty acids |
setSize | 8 |
pANOVA | 0.0116 |
s.dist | -0.515 |
p.adjustANOVA | 0.199 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
LCN12 | -10907 |
LCN15 | -10389 |
SLC27A6 | -9987 |
SLC27A1 | -9293 |
SLC27A4 | -6419 |
LCN1 | -4541 |
LCN9 | -2875 |
APOD | 9813 |
GeneID | Gene Rank |
---|---|
LCN12 | -10907 |
LCN15 | -10389 |
SLC27A6 | -9987 |
SLC27A1 | -9293 |
SLC27A4 | -6419 |
LCN1 | -4541 |
LCN9 | -2875 |
APOD | 9813 |
Inhibition of Signaling by Overexpressed EGFR
786 | |
---|---|
set | Inhibition of Signaling by Overexpressed EGFR |
setSize | 8 |
pANOVA | 0.0122 |
s.dist | -0.512 |
p.adjustANOVA | 0.206 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
EPGN | -10955 |
AREG | -10924 |
EREG | -9691 |
BTC | -6076 |
EGFR | -3464 |
EGF | -3037 |
HBEGF | -1421 |
TGFA | 1329 |
GeneID | Gene Rank |
---|---|
EPGN | -10955 |
AREG | -10924 |
EREG | -9691 |
BTC | -6076 |
EGFR | -3464 |
EGF | -3037 |
HBEGF | -1421 |
TGFA | 1329 |
Signaling by Overexpressed Wild-Type EGFR in Cancer
1668 | |
---|---|
set | Signaling by Overexpressed Wild-Type EGFR in Cancer |
setSize | 8 |
pANOVA | 0.0122 |
s.dist | -0.512 |
p.adjustANOVA | 0.206 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
EPGN | -10955 |
AREG | -10924 |
EREG | -9691 |
BTC | -6076 |
EGFR | -3464 |
EGF | -3037 |
HBEGF | -1421 |
TGFA | 1329 |
GeneID | Gene Rank |
---|---|
EPGN | -10955 |
AREG | -10924 |
EREG | -9691 |
BTC | -6076 |
EGFR | -3464 |
EGF | -3037 |
HBEGF | -1421 |
TGFA | 1329 |
Conjugation of benzoate with glycine
306 | |
---|---|
set | Conjugation of benzoate with glycine |
setSize | 6 |
pANOVA | 0.0327 |
s.dist | 0.503 |
p.adjustANOVA | 0.318 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
ACSM2B | 11530 |
ACSM1 | 11167 |
GLYAT | 9490 |
GLYATL2 | 6889 |
GLYATL3 | -223 |
GLYATL1 | -1926 |
GeneID | Gene Rank |
---|---|
ACSM2B | 11530 |
ACSM1 | 11167 |
GLYAT | 9490 |
GLYATL2 | 6889 |
GLYATL3 | -223 |
GLYATL1 | -1926 |
Sulfide oxidation to sulfate
1719 | |
---|---|
set | Sulfide oxidation to sulfate |
setSize | 5 |
pANOVA | 0.0514 |
s.dist | -0.503 |
p.adjustANOVA | 0.379 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
TSTD1 | -10692 |
SLC25A10 | -10257 |
TST | -8492 |
SUOX | -2745 |
ETHE1 | 5027 |
GeneID | Gene Rank |
---|---|
TSTD1 | -10692 |
SLC25A10 | -10257 |
TST | -8492 |
SUOX | -2745 |
ETHE1 | 5027 |
Expression and translocation of olfactory receptors
528 | |
---|---|
set | Expression and translocation of olfactory receptors |
setSize | 334 |
pANOVA | 1.38e-55 |
s.dist | 0.498 |
p.adjustANOVA | 2.78e-52 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
OR56B1 | 11868 |
OR7D2 | 11861 |
OR52M1 | 11855 |
OR6Q1 | 11852 |
OR1J4 | 11847 |
OR1L1 | 11843 |
OR6C75 | 11837 |
OR51B4 | 11836 |
OR5B21 | 11833 |
OR51V1 | 11821 |
OR5H6 | 11811 |
OR10S1 | 11808 |
OR4A47 | 11806 |
OR1S1 | 11804 |
OR4B1 | 11803 |
OR2A25 | 11802 |
OR5K4 | 11798 |
OR52B2 | 11797 |
OR4D2 | 11787 |
OR6C70 | 11784 |
GeneID | Gene Rank |
---|---|
OR56B1 | 11868.0 |
OR7D2 | 11861.0 |
OR52M1 | 11855.0 |
OR6Q1 | 11852.0 |
OR1J4 | 11847.0 |
OR1L1 | 11843.0 |
OR6C75 | 11837.0 |
OR51B4 | 11836.0 |
OR5B21 | 11833.0 |
OR51V1 | 11821.0 |
OR5H6 | 11811.0 |
OR10S1 | 11808.0 |
OR4A47 | 11806.0 |
OR1S1 | 11804.0 |
OR4B1 | 11803.0 |
OR2A25 | 11802.0 |
OR5K4 | 11798.0 |
OR52B2 | 11797.0 |
OR4D2 | 11787.0 |
OR6C70 | 11784.0 |
OR1J2 | 11765.0 |
OR1Q1 | 11751.0 |
OR56A3 | 11738.0 |
OR51L1 | 11734.0 |
OR52N2 | 11725.0 |
OR1B1 | 11723.0 |
OR51B2 | 11722.0 |
OR1I1 | 11714.0 |
OR52N1 | 11706.0 |
OR4K15 | 11690.0 |
OR52D1 | 11689.0 |
OR52A1 | 11686.0 |
OR10H1 | 11685.0 |
OR2F2 | 11665.0 |
OR4D11 | 11659.0 |
OR10A7 | 11654.0 |
OR5B12 | 11650.0 |
OR10H3 | 11649.0 |
OR4E2 | 11641.0 |
OR8B12 | 11638.0 |
OR4D1 | 11615.0 |
OR9A2 | 11612.0 |
OR4C6 | 11611.0 |
OR5K2 | 11605.0 |
OR5M10 | 11596.0 |
OR4N4 | 11573.0 |
OR2J2 | 11572.0 |
OR2A5 | 11552.0 |
OR5K3 | 11549.0 |
OR52A5 | 11546.0 |
OR1L4 | 11534.0 |
OR5D13 | 11525.0 |
OR6C6 | 11516.0 |
OR2F1 | 11514.0 |
OR8H3 | 11512.0 |
OR1L3 | 11510.0 |
OR6S1 | 11495.0 |
OR10H4 | 11490.0 |
OR6C4 | 11485.0 |
OR51I1 | 11474.0 |
OR9K2 | 11472.0 |
OR4A16 | 11470.0 |
OR4S2 | 11469.0 |
OR4X2 | 11466.0 |
OR52E6 | 11455.0 |
OR5B2 | 11447.0 |
OR56A5 | 11438.0 |
OR4S1 | 11422.0 |
OR1M1 | 11417.0 |
OR4X1 | 11414.0 |
OR4C16 | 11402.0 |
OR4D6 | 11400.0 |
OR9A4 | 11399.0 |
OR10A6 | 11392.0 |
OR6T1 | 11369.0 |
OR52H1 | 11353.0 |
OR2D2 | 11352.0 |
OR4M2 | 11340.0 |
OR4C13 | 11338.0 |
OR7G2 | 11331.0 |
OR5L1 | 11329.0 |
OR51F1 | 11328.0 |
OR5AU1 | 11318.0 |
OR13C4 | 11302.0 |
OR1N2 | 11285.0 |
OR8D1 | 11270.0 |
OR4K14 | 11268.0 |
OR5M3 | 11259.0 |
OR52N5 | 11258.0 |
OR10A3 | 11252.0 |
OR6X1 | 11247.0 |
OR6M1 | 11238.0 |
OR5A2 | 11230.0 |
OR51M1 | 11215.0 |
OR10G2 | 11198.0 |
OR51B5 | 11197.0 |
OR5F1 | 11179.0 |
OR5V1 | 11173.0 |
OR5B17 | 11145.0 |
OR51G1 | 11127.0 |
OR6P1 | 11123.0 |
OR51G2 | 11095.0 |
OR4K13 | 11040.0 |
OR12D2 | 11039.0 |
OR5H2 | 11036.0 |
OR6B1 | 11021.0 |
OR10H2 | 11010.0 |
OR4K2 | 10994.0 |
OR10X1 | 10983.0 |
OR10G9 | 10980.0 |
OR51Q1 | 10969.0 |
OR10W1 | 10934.0 |
OR5P3 | 10926.0 |
OR6C2 | 10923.0 |
OR52E8 | 10918.0 |
OR5H1 | 10908.0 |
OR10H5 | 10880.0 |
OR5A1 | 10867.0 |
OR4C3 | 10850.0 |
OR2C1 | 10843.0 |
OR56A1 | 10831.0 |
OR7G1 | 10820.0 |
OR9Q2 | 10808.0 |
OR52R1 | 10803.0 |
OR7G3 | 10801.0 |
OR10A5 | 10784.0 |
OR1N1 | 10764.0 |
OR1G1 | 10763.0 |
OR2H1 | 10743.0 |
OR52K2 | 10724.0 |
OR2AP1 | 10711.0 |
OR11H4 | 10707.0 |
OR5I1 | 10706.0 |
OR10A4 | 10683.0 |
OR51T1 | 10668.0 |
OR52I2 | 10666.0 |
OR9Q1 | 10662.0 |
OR5D18 | 10613.0 |
OR4C46 | 10611.0 |
OR5AC2 | 10601.0 |
OR5AS1 | 10588.0 |
OR5M11 | 10581.0 |
OR6A2 | 10529.0 |
OR51E1 | 10527.0 |
OR4F15 | 10526.0 |
OR5D16 | 10485.0 |
OR12D3 | 10482.0 |
OR13C3 | 10453.0 |
OR56A4 | 10450.0 |
OR9G4 | 10368.0 |
OR10AD1 | 10357.0 |
OR10J3 | 10353.0 |
OR1E1 | 10339.0 |
OR2W1 | 10331.0 |
OR4K1 | 10295.0 |
OR52J3 | 10285.0 |
OR5AK2 | 10251.0 |
OR4A15 | 10179.0 |
OR52I1 | 10169.0 |
OR51F2 | 10154.0 |
OR4M1 | 10143.0 |
OR5J2 | 10142.0 |
OR3A3 | 10091.0 |
OR6K6 | 10071.0 |
OR2AG2 | 10008.0 |
OR9G1 | 9980.5 |
OR9G9 | 9980.5 |
OR10G7 | 9958.0 |
OR5B3 | 9928.0 |
RTP1 | 9911.0 |
OR4K17 | 9900.0 |
OR6V1 | 9876.0 |
OR6N1 | 9702.0 |
OR8K1 | 9651.0 |
OR51E2 | 9621.0 |
OR13A1 | 9484.0 |
OR10G4 | 9445.0 |
OR8K3 | 9409.0 |
OR6Y1 | 9399.0 |
OR10P1 | 9325.0 |
OR2B3 | 9273.0 |
OR6B2 | 9256.0 |
OR4K5 | 9239.0 |
OR56B4 | 9230.0 |
OR2B2 | 9139.0 |
OR8A1 | 9124.0 |
OR8D4 | 9013.0 |
OR51S1 | 8986.0 |
OR7D4 | 8917.0 |
OR14J1 | 8806.0 |
OR10C1 | 8804.0 |
OR6C74 | 8717.0 |
OR4D9 | 8636.0 |
OR10J1 | 8593.0 |
OR6C65 | 8592.0 |
RTP2 | 8588.0 |
OR7A17 | 8492.0 |
OR51B6 | 8418.0 |
OR6C3 | 8262.0 |
OR51D1 | 8235.0 |
OR4D5 | 8095.0 |
OR8U8 | 8007.0 |
OR6B3 | 7939.0 |
OR1A1 | 7809.0 |
OR5AP2 | 7773.0 |
OR2D3 | 7756.0 |
OR2Z1 | 7613.0 |
OR7A5 | 7551.0 |
OR1L8 | 7513.0 |
OR10J5 | 7468.0 |
OR10Q1 | 7334.0 |
OR7C2 | 7174.0 |
OR10K2 | 7140.0 |
OR8H1 | 7084.0 |
OR52B6 | 7075.0 |
OR51I2 | 6931.0 |
OR4N2 | 6601.0 |
OR2AT4 | 6409.0 |
OR8S1 | 6266.0 |
OR5P2 | 6133.0 |
OR4N5 | 6049.0 |
OR10AG1 | 5969.0 |
OR10G3 | 5882.0 |
OR2A12 | 5755.0 |
OR6K3 | 5670.0 |
OR52L1 | 5651.0 |
OR13C9 | 5579.0 |
OR10Z1 | 5438.0 |
OR10G8 | 5385.0 |
OR6K2 | 5328.0 |
OR9I1 | 5183.0 |
OR2AG1 | 4991.0 |
OR14I1 | 4818.0 |
OR13F1 | 4678.0 |
OR11A1 | 4605.0 |
OR52E2 | 4414.0 |
OR10V1 | 4330.0 |
OR2A2 | 4055.0 |
OR10T2 | 3691.0 |
OR52K1 | 3508.0 |
OR8U1 | 3487.0 |
OR52A4P | 3458.0 |
OR1E2 | 3427.0 |
OR11G2 | 3418.0 |
OR4C12 | 3240.0 |
OR8G5 | 2878.0 |
OR8H2 | 2776.0 |
OR1D2 | 2630.0 |
OR8B8 | 2529.0 |
OR2T11 | 2083.0 |
EBF1 | 1813.0 |
OR5C1 | 1808.0 |
OR1S2 | 1505.0 |
OR5W2 | 1352.0 |
OR1F1 | 1307.0 |
OR2Y1 | 1186.0 |
OR13H1 | 933.0 |
OR2AK2 | 739.0 |
OR3A1 | 620.0 |
OR5M8 | 558.0 |
OR2T1 | 378.0 |
OR2K2 | 238.0 |
REEP1 | 43.0 |
OR8I2 | 22.0 |
OR4D10 | 12.0 |
OR11H6 | -117.0 |
OR6C1 | -188.0 |
OR6N2 | -325.0 |
OR1K1 | -362.0 |
OR2T34 | -421.0 |
OR14C36 | -862.0 |
LHX2 | -973.0 |
LDB1 | -1210.0 |
OR7A10 | -1468.0 |
OR51A2 | -1578.0 |
OR4L1 | -1581.0 |
OR4C15 | -1607.0 |
OR1A2 | -2413.0 |
OR2B6 | -2617.0 |
OR8B4 | -2660.0 |
OR8G1 | -3327.0 |
OR8U3 | -3468.0 |
OR2M5 | -3757.0 |
OR51A7 | -4079.0 |
OR2T10 | -4152.0 |
OR2L2 | -4307.0 |
OR2M2 | -4478.0 |
OR14A16 | -4532.0 |
OR2W3 | -4552.0 |
OR6C68 | -4579.0 |
OR5L2 | -4826.0 |
OR2G3 | -5512.0 |
OR2V2 | -5566.0 |
OR2S2 | -5815.0 |
OR11L1 | -6130.0 |
OR5D14 | -6433.0 |
OR7C1 | -6886.0 |
OR2L13 | -6909.0 |
OR2T8 | -6989.0 |
OR3A2 | -7170.0 |
OR2G6 | -7286.0 |
OR2B11 | -7544.0 |
OR8D2 | -7687.0 |
OR2G2 | -7760.0 |
OR5AR1 | -8061.0 |
OR8K5 | -8139.0 |
OR4A5 | -8487.0 |
OR52W1 | -8905.0 |
OR1L6 | -8970.0 |
OR2T6 | -8985.0 |
OR2V1 | -9033.0 |
OR2M4 | -9065.0 |
OR1J1 | -9068.0 |
OR2H2 | -9272.0 |
OR2T3 | -9750.0 |
OR7E24 | -9843.0 |
OR2T33 | -9879.0 |
OR4F6 | -10019.0 |
OR10A2 | -10079.0 |
OR2AE1 | -10087.0 |
OR13G1 | -10214.0 |
OR2M3 | -10227.0 |
OR6F1 | -10268.0 |
OR8B2 | -10420.0 |
OR5T3 | -10562.0 |
OR10K1 | -10572.0 |
OR2C3 | -10574.0 |
OR1C1 | -10594.0 |
OR2A14 | -10615.0 |
OR2L8 | -10743.0 |
OR2T27 | -10746.0 |
OR13J1 | -10833.0 |
OR2L3 | -10892.0 |
OR2T4 | -10973.0 |
Nef Mediated CD4 Down-regulation
1055 | |
---|---|
set | Nef Mediated CD4 Down-regulation |
setSize | 9 |
pANOVA | 0.011 |
s.dist | -0.49 |
p.adjustANOVA | 0.195 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
AP2A2 | -10138 |
CD4 | -8591 |
AP2M1 | -7849 |
LCK | -7785 |
AP2A1 | -6828 |
AP2S1 | -5603 |
ARF1 | -3650 |
AP2B1 | -672 |
ATP6V1H | 3615 |
GeneID | Gene Rank |
---|---|
AP2A2 | -10138 |
CD4 | -8591 |
AP2M1 | -7849 |
LCK | -7785 |
AP2A1 | -6828 |
AP2S1 | -5603 |
ARF1 | -3650 |
AP2B1 | -672 |
ATP6V1H | 3615 |
Olfactory Signaling Pathway
1124 | |
---|---|
set | Olfactory Signaling Pathway |
setSize | 342 |
pANOVA | 4.61e-54 |
s.dist | 0.486 |
p.adjustANOVA | 4.64e-51 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
OR56B1 | 11868 |
OR7D2 | 11861 |
OR52M1 | 11855 |
OR6Q1 | 11852 |
OR1J4 | 11847 |
OR1L1 | 11843 |
OR6C75 | 11837 |
OR51B4 | 11836 |
OR5B21 | 11833 |
OR51V1 | 11821 |
OR5H6 | 11811 |
OR10S1 | 11808 |
OR4A47 | 11806 |
OR1S1 | 11804 |
OR4B1 | 11803 |
OR2A25 | 11802 |
OR5K4 | 11798 |
OR52B2 | 11797 |
OR4D2 | 11787 |
OR6C70 | 11784 |
GeneID | Gene Rank |
---|---|
OR56B1 | 11868.0 |
OR7D2 | 11861.0 |
OR52M1 | 11855.0 |
OR6Q1 | 11852.0 |
OR1J4 | 11847.0 |
OR1L1 | 11843.0 |
OR6C75 | 11837.0 |
OR51B4 | 11836.0 |
OR5B21 | 11833.0 |
OR51V1 | 11821.0 |
OR5H6 | 11811.0 |
OR10S1 | 11808.0 |
OR4A47 | 11806.0 |
OR1S1 | 11804.0 |
OR4B1 | 11803.0 |
OR2A25 | 11802.0 |
OR5K4 | 11798.0 |
OR52B2 | 11797.0 |
OR4D2 | 11787.0 |
OR6C70 | 11784.0 |
OR1J2 | 11765.0 |
OR1Q1 | 11751.0 |
OR56A3 | 11738.0 |
OR51L1 | 11734.0 |
OR52N2 | 11725.0 |
OR1B1 | 11723.0 |
OR51B2 | 11722.0 |
OR1I1 | 11714.0 |
OR52N1 | 11706.0 |
OR4K15 | 11690.0 |
OR52D1 | 11689.0 |
OR52A1 | 11686.0 |
OR10H1 | 11685.0 |
OR2F2 | 11665.0 |
OR4D11 | 11659.0 |
OR10A7 | 11654.0 |
OR5B12 | 11650.0 |
OR10H3 | 11649.0 |
OR4E2 | 11641.0 |
OR8B12 | 11638.0 |
OR4D1 | 11615.0 |
OR9A2 | 11612.0 |
OR4C6 | 11611.0 |
OR5K2 | 11605.0 |
OR5M10 | 11596.0 |
OR4N4 | 11573.0 |
OR2J2 | 11572.0 |
OR2A5 | 11552.0 |
OR5K3 | 11549.0 |
OR52A5 | 11546.0 |
OR1L4 | 11534.0 |
OR5D13 | 11525.0 |
OR6C6 | 11516.0 |
OR2F1 | 11514.0 |
OR8H3 | 11512.0 |
OR1L3 | 11510.0 |
OR6S1 | 11495.0 |
OR10H4 | 11490.0 |
OR6C4 | 11485.0 |
OR51I1 | 11474.0 |
OR9K2 | 11472.0 |
OR4A16 | 11470.0 |
OR4S2 | 11469.0 |
OR4X2 | 11466.0 |
OR52E6 | 11455.0 |
OR5B2 | 11447.0 |
OR56A5 | 11438.0 |
OR4S1 | 11422.0 |
OR1M1 | 11417.0 |
OR4X1 | 11414.0 |
OR4C16 | 11402.0 |
OR4D6 | 11400.0 |
OR9A4 | 11399.0 |
OR10A6 | 11392.0 |
OR6T1 | 11369.0 |
OR52H1 | 11353.0 |
OR2D2 | 11352.0 |
OR4M2 | 11340.0 |
OR4C13 | 11338.0 |
OR7G2 | 11331.0 |
OR5L1 | 11329.0 |
OR51F1 | 11328.0 |
OR5AU1 | 11318.0 |
OR13C4 | 11302.0 |
OR1N2 | 11285.0 |
OR8D1 | 11270.0 |
OR4K14 | 11268.0 |
OR5M3 | 11259.0 |
OR52N5 | 11258.0 |
OR10A3 | 11252.0 |
OR6X1 | 11247.0 |
OR6M1 | 11238.0 |
OR5A2 | 11230.0 |
OR51M1 | 11215.0 |
OR10G2 | 11198.0 |
OR51B5 | 11197.0 |
OR5F1 | 11179.0 |
OR5V1 | 11173.0 |
OR5B17 | 11145.0 |
OR51G1 | 11127.0 |
OR6P1 | 11123.0 |
OR51G2 | 11095.0 |
OR4K13 | 11040.0 |
OR12D2 | 11039.0 |
OR5H2 | 11036.0 |
OR6B1 | 11021.0 |
OR10H2 | 11010.0 |
OR4K2 | 10994.0 |
OR10X1 | 10983.0 |
OR10G9 | 10980.0 |
OR51Q1 | 10969.0 |
OR10W1 | 10934.0 |
OR5P3 | 10926.0 |
OR6C2 | 10923.0 |
OR52E8 | 10918.0 |
OR5H1 | 10908.0 |
OR10H5 | 10880.0 |
OR5A1 | 10867.0 |
OR4C3 | 10850.0 |
OR2C1 | 10843.0 |
OR56A1 | 10831.0 |
OR7G1 | 10820.0 |
OR9Q2 | 10808.0 |
OR52R1 | 10803.0 |
OR7G3 | 10801.0 |
OR10A5 | 10784.0 |
OR1N1 | 10764.0 |
OR1G1 | 10763.0 |
OR2H1 | 10743.0 |
OR52K2 | 10724.0 |
OR2AP1 | 10711.0 |
OR11H4 | 10707.0 |
OR5I1 | 10706.0 |
OR10A4 | 10683.0 |
OR51T1 | 10668.0 |
OR52I2 | 10666.0 |
OR9Q1 | 10662.0 |
OR5D18 | 10613.0 |
OR4C46 | 10611.0 |
OR5AC2 | 10601.0 |
OR5AS1 | 10588.0 |
OR5M11 | 10581.0 |
OR6A2 | 10529.0 |
OR51E1 | 10527.0 |
OR4F15 | 10526.0 |
OR5D16 | 10485.0 |
OR12D3 | 10482.0 |
OR13C3 | 10453.0 |
OR56A4 | 10450.0 |
OR9G4 | 10368.0 |
OR10AD1 | 10357.0 |
OR10J3 | 10353.0 |
OR1E1 | 10339.0 |
OR2W1 | 10331.0 |
OR4K1 | 10295.0 |
OR52J3 | 10285.0 |
OR5AK2 | 10251.0 |
OR4A15 | 10179.0 |
OR52I1 | 10169.0 |
OR51F2 | 10154.0 |
OR4M1 | 10143.0 |
OR5J2 | 10142.0 |
OR3A3 | 10091.0 |
OR6K6 | 10071.0 |
OR2AG2 | 10008.0 |
OR9G1 | 9980.5 |
OR9G9 | 9980.5 |
OR10G7 | 9958.0 |
OR5B3 | 9928.0 |
RTP1 | 9911.0 |
OR4K17 | 9900.0 |
OR6V1 | 9876.0 |
OR6N1 | 9702.0 |
OR8K1 | 9651.0 |
OR51E2 | 9621.0 |
OR13A1 | 9484.0 |
OR10G4 | 9445.0 |
OR8K3 | 9409.0 |
OR6Y1 | 9399.0 |
OR10P1 | 9325.0 |
OR2B3 | 9273.0 |
CNGA4 | 9259.0 |
OR6B2 | 9256.0 |
OR4K5 | 9239.0 |
OR56B4 | 9230.0 |
OR2B2 | 9139.0 |
OR8A1 | 9124.0 |
OR8D4 | 9013.0 |
OR51S1 | 8986.0 |
OR7D4 | 8917.0 |
OR14J1 | 8806.0 |
OR10C1 | 8804.0 |
OR6C74 | 8717.0 |
OR4D9 | 8636.0 |
OR10J1 | 8593.0 |
OR6C65 | 8592.0 |
RTP2 | 8588.0 |
OR7A17 | 8492.0 |
OR51B6 | 8418.0 |
OR6C3 | 8262.0 |
OR51D1 | 8235.0 |
OR4D5 | 8095.0 |
OR8U8 | 8007.0 |
OR6B3 | 7939.0 |
OR1A1 | 7809.0 |
OR5AP2 | 7773.0 |
OR2D3 | 7756.0 |
OR2Z1 | 7613.0 |
OR7A5 | 7551.0 |
OR1L8 | 7513.0 |
OR10J5 | 7468.0 |
ANO2 | 7351.0 |
OR10Q1 | 7334.0 |
OR7C2 | 7174.0 |
OR10K2 | 7140.0 |
OR8H1 | 7084.0 |
OR52B6 | 7075.0 |
OR51I2 | 6931.0 |
GNG13 | 6603.0 |
OR4N2 | 6601.0 |
OR2AT4 | 6409.0 |
OR8S1 | 6266.0 |
OR5P2 | 6133.0 |
OR4N5 | 6049.0 |
OR10AG1 | 5969.0 |
OR10G3 | 5882.0 |
OR2A12 | 5755.0 |
OR6K3 | 5670.0 |
OR52L1 | 5651.0 |
OR13C9 | 5579.0 |
OR10Z1 | 5438.0 |
OR10G8 | 5385.0 |
OR6K2 | 5328.0 |
OR9I1 | 5183.0 |
OR2AG1 | 4991.0 |
OR14I1 | 4818.0 |
OR13F1 | 4678.0 |
OR11A1 | 4605.0 |
OR52E2 | 4414.0 |
OR10V1 | 4330.0 |
OR2A2 | 4055.0 |
OR10T2 | 3691.0 |
OR52K1 | 3508.0 |
OR8U1 | 3487.0 |
OR52A4P | 3458.0 |
OR1E2 | 3427.0 |
OR11G2 | 3418.0 |
OR4C12 | 3240.0 |
OR8G5 | 2878.0 |
OR8H2 | 2776.0 |
OR1D2 | 2630.0 |
OR8B8 | 2529.0 |
OR2T11 | 2083.0 |
EBF1 | 1813.0 |
OR5C1 | 1808.0 |
OR1S2 | 1505.0 |
OR5W2 | 1352.0 |
OR1F1 | 1307.0 |
OR2Y1 | 1186.0 |
CNGA2 | 1023.0 |
OR13H1 | 933.0 |
OR2AK2 | 739.0 |
OR3A1 | 620.0 |
OR5M8 | 558.0 |
OR2T1 | 378.0 |
OR2K2 | 238.0 |
REEP1 | 43.0 |
OR8I2 | 22.0 |
OR4D10 | 12.0 |
OR11H6 | -117.0 |
OR6C1 | -188.0 |
OR6N2 | -325.0 |
OR1K1 | -362.0 |
OR2T34 | -421.0 |
OR14C36 | -862.0 |
LHX2 | -973.0 |
LDB1 | -1210.0 |
OR7A10 | -1468.0 |
OR51A2 | -1578.0 |
OR4L1 | -1581.0 |
OR4C15 | -1607.0 |
OR1A2 | -2413.0 |
OR2B6 | -2617.0 |
OR8B4 | -2660.0 |
OR8G1 | -3327.0 |
OR8U3 | -3468.0 |
OR2M5 | -3757.0 |
CNGB1 | -3831.0 |
OR51A7 | -4079.0 |
OR2T10 | -4152.0 |
OR2L2 | -4307.0 |
OR2M2 | -4478.0 |
OR14A16 | -4532.0 |
OR2W3 | -4552.0 |
OR6C68 | -4579.0 |
GNAL | -4709.0 |
OR5L2 | -4826.0 |
OR2G3 | -5512.0 |
OR2V2 | -5566.0 |
OR2S2 | -5815.0 |
OR11L1 | -6130.0 |
OR5D14 | -6433.0 |
OR7C1 | -6886.0 |
OR2L13 | -6909.0 |
OR2T8 | -6989.0 |
OR3A2 | -7170.0 |
OR2G6 | -7286.0 |
OR2B11 | -7544.0 |
OR8D2 | -7687.0 |
OR2G2 | -7760.0 |
OR5AR1 | -8061.0 |
OR8K5 | -8139.0 |
OR4A5 | -8487.0 |
ADCY3 | -8634.0 |
OR52W1 | -8905.0 |
OR1L6 | -8970.0 |
OR2T6 | -8985.0 |
OR2V1 | -9033.0 |
OR2M4 | -9065.0 |
OR1J1 | -9068.0 |
GNB1 | -9151.0 |
OR2H2 | -9272.0 |
OR2T3 | -9750.0 |
OR7E24 | -9843.0 |
OR2T33 | -9879.0 |
OR4F6 | -10019.0 |
OR10A2 | -10079.0 |
OR2AE1 | -10087.0 |
OR13G1 | -10214.0 |
OR2M3 | -10227.0 |
OR6F1 | -10268.0 |
OR8B2 | -10420.0 |
OR5T3 | -10562.0 |
OR10K1 | -10572.0 |
OR2C3 | -10574.0 |
OR1C1 | -10594.0 |
OR2A14 | -10615.0 |
OR2L8 | -10743.0 |
OR2T27 | -10746.0 |
OR13J1 | -10833.0 |
OR2L3 | -10892.0 |
OR2T4 | -10973.0 |
Reelin signalling pathway
1402 | |
---|---|
set | Reelin signalling pathway |
setSize | 5 |
pANOVA | 0.0608 |
s.dist | 0.484 |
p.adjustANOVA | 0.391 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
RELN | 9541 |
DAB1 | 8124 |
VLDLR | 7176 |
SH3KBP1 | 4708 |
FYN | 112 |
GeneID | Gene Rank |
---|---|
RELN | 9541 |
DAB1 | 8124 |
VLDLR | 7176 |
SH3KBP1 | 4708 |
FYN | 112 |
Biosynthesis of maresin-like SPMs
177 | |
---|---|
set | Biosynthesis of maresin-like SPMs |
setSize | 6 |
pANOVA | 0.0423 |
s.dist | 0.479 |
p.adjustANOVA | 0.361 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CYP2C8 | 11395 |
CYP3A4 | 9179 |
CYP1A2 | 8556 |
CYP2D6 | 7364 |
CYP2E1 | 2280 |
CYP2C9 | -3558 |
GeneID | Gene Rank |
---|---|
CYP2C8 | 11395 |
CYP3A4 | 9179 |
CYP1A2 | 8556 |
CYP2D6 | 7364 |
CYP2E1 | 2280 |
CYP2C9 | -3558 |
Beta defensins
159 | |
---|---|
set | Beta defensins |
setSize | 27 |
pANOVA | 2.03e-05 |
s.dist | 0.474 |
p.adjustANOVA | 0.00488 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CCR2 | 11662.0 |
DEFB133 | 11599.0 |
DEFB113 | 11464.0 |
DEFB116 | 11371.0 |
DEFB119 | 11287.0 |
DEFB118 | 11237.0 |
DEFB114 | 11213.0 |
DEFB103A | 11037.5 |
DEFB121 | 10678.0 |
TLR1 | 10582.0 |
DEFB135 | 10406.0 |
DEFB136 | 10072.0 |
DEFB124 | 9944.0 |
DEFB123 | 7664.0 |
CCR6 | 6450.0 |
DEFB115 | 6231.0 |
DEFB125 | 5903.0 |
DEFB126 | 4995.0 |
DEFB128 | 2190.0 |
DEFB127 | 1288.0 |
GeneID | Gene Rank |
---|---|
CCR2 | 11662.0 |
DEFB133 | 11599.0 |
DEFB113 | 11464.0 |
DEFB116 | 11371.0 |
DEFB119 | 11287.0 |
DEFB118 | 11237.0 |
DEFB114 | 11213.0 |
DEFB103A | 11037.5 |
DEFB121 | 10678.0 |
TLR1 | 10582.0 |
DEFB135 | 10406.0 |
DEFB136 | 10072.0 |
DEFB124 | 9944.0 |
DEFB123 | 7664.0 |
CCR6 | 6450.0 |
DEFB115 | 6231.0 |
DEFB125 | 5903.0 |
DEFB126 | 4995.0 |
DEFB128 | 2190.0 |
DEFB127 | 1288.0 |
DEFB108B | 239.0 |
DEFB132 | -276.0 |
DEFB129 | -1733.0 |
DEFB104A | -3835.5 |
DEFB1 | -4158.0 |
TLR2 | -5282.0 |
DEFB134 | -5459.0 |
E2F-enabled inhibition of pre-replication complex formation
474 | |
---|---|
set | E2F-enabled inhibition of pre-replication complex formation |
setSize | 9 |
pANOVA | 0.0144 |
s.dist | 0.471 |
p.adjustANOVA | 0.222 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
ORC1 | 9482 |
ORC4 | 9117 |
CCNB1 | 8805 |
MCM8 | 7131 |
ORC6 | 7057 |
ORC3 | 6686 |
CDK1 | 2115 |
ORC5 | 1579 |
ORC2 | 56 |
GeneID | Gene Rank |
---|---|
ORC1 | 9482 |
ORC4 | 9117 |
CCNB1 | 8805 |
MCM8 | 7131 |
ORC6 | 7057 |
ORC3 | 6686 |
CDK1 | 2115 |
ORC5 | 1579 |
ORC2 | 56 |
OAS antiviral response
1123 | |
---|---|
set | OAS antiviral response |
setSize | 9 |
pANOVA | 0.0149 |
s.dist | -0.469 |
p.adjustANOVA | 0.223 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
FLNA | -9886 |
OASL | -8373 |
OAS1 | -8225 |
PDE12 | -5925 |
OAS3 | -5485 |
RNASEL | -5098 |
OAS2 | -3339 |
RIGI | -2335 |
ABCE1 | 3319 |
GeneID | Gene Rank |
---|---|
FLNA | -9886 |
OASL | -8373 |
OAS1 | -8225 |
PDE12 | -5925 |
OAS3 | -5485 |
RNASEL | -5098 |
OAS2 | -3339 |
RIGI | -2335 |
ABCE1 | 3319 |
Defective LFNG causes SCDO3
388 | |
---|---|
set | Defective LFNG causes SCDO3 |
setSize | 5 |
pANOVA | 0.0727 |
s.dist | -0.463 |
p.adjustANOVA | 0.425 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
NOTCH3 | -8566 |
NOTCH1 | -6878 |
NOTCH2 | -4991 |
NOTCH4 | -3533 |
LFNG | -913 |
GeneID | Gene Rank |
---|---|
NOTCH3 | -8566 |
NOTCH1 | -6878 |
NOTCH2 | -4991 |
NOTCH4 | -3533 |
LFNG | -913 |
NR1H2 & NR1H3 regulate gene expression linked to triglyceride
lipolysis in adipose
1043 | |
---|---|
set | NR1H2 & NR1H3 regulate gene expression linked to triglyceride lipolysis in adipose |
setSize | 5 |
pANOVA | 0.0732 |
s.dist | -0.463 |
p.adjustANOVA | 0.425 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
RXRA | -8542 |
PLIN1 | -8440 |
NR1H3 | -7376 |
RXRB | -4473 |
NR1H2 | 3993 |
GeneID | Gene Rank |
---|---|
RXRA | -8542 |
PLIN1 | -8440 |
NR1H3 | -7376 |
RXRB | -4473 |
NR1H2 | 3993 |
GRB7 events in ERBB2 signaling
654 | |
---|---|
set | GRB7 events in ERBB2 signaling |
setSize | 5 |
pANOVA | 0.0747 |
s.dist | -0.46 |
p.adjustANOVA | 0.428 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
GRB7 | -10645 |
ERBB2 | -10029 |
NRG2 | -6779 |
ERBB3 | -4313 |
NRG1 | 7066 |
GeneID | Gene Rank |
---|---|
GRB7 | -10645 |
ERBB2 | -10029 |
NRG2 | -6779 |
ERBB3 | -4313 |
NRG1 | 7066 |
Regulation of CDH19 Expression and Function
1413 | |
---|---|
set | Regulation of CDH19 Expression and Function |
setSize | 7 |
pANOVA | 0.0352 |
s.dist | -0.46 |
p.adjustANOVA | 0.327 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
SOX10 | -10919 |
CTNND1 | -10434 |
JUP | -10168 |
ZC3H12A | -6832 |
CTNNA1 | -4601 |
CTNNB1 | -333 |
CDH19 | 8758 |
GeneID | Gene Rank |
---|---|
SOX10 | -10919 |
CTNND1 | -10434 |
JUP | -10168 |
ZC3H12A | -6832 |
CTNNA1 | -4601 |
CTNNB1 | -333 |
CDH19 | 8758 |
Sema4D mediated inhibition of cell attachment and migration
1581 | |
---|---|
set | Sema4D mediated inhibition of cell attachment and migration |
setSize | 8 |
pANOVA | 0.0256 |
s.dist | -0.456 |
p.adjustANOVA | 0.283 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
PLXNB1 | -10414 |
RND1 | -8867 |
ARHGAP35 | -8321 |
RAC1 | -6548 |
RHOA | -4849 |
SEMA4D | -4394 |
RRAS | -2815 |
MET | 7112 |
GeneID | Gene Rank |
---|---|
PLXNB1 | -10414 |
RND1 | -8867 |
ARHGAP35 | -8321 |
RAC1 | -6548 |
RHOA | -4849 |
SEMA4D | -4394 |
RRAS | -2815 |
MET | 7112 |
NFE2L2 regulating tumorigenic genes
1027 | |
---|---|
set | NFE2L2 regulating tumorigenic genes |
setSize | 11 |
pANOVA | 0.00918 |
s.dist | -0.454 |
p.adjustANOVA | 0.181 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
AREG | -10924 |
PDGFA | -8837 |
CREBBP | -8768 |
BCL2L1 | -7957 |
NOTCH1 | -6878 |
SP1 | -4222 |
BCL2 | -4180 |
EGF | -3037 |
MAFK | -1852 |
EP300 | 1142 |
NFE2L2 | 2024 |
GeneID | Gene Rank |
---|---|
AREG | -10924 |
PDGFA | -8837 |
CREBBP | -8768 |
BCL2L1 | -7957 |
NOTCH1 | -6878 |
SP1 | -4222 |
BCL2 | -4180 |
EGF | -3037 |
MAFK | -1852 |
EP300 | 1142 |
NFE2L2 | 2024 |
Regulation of gene expression in endocrine-committed (NEUROG3+)
progenitor cells
1460 | |
---|---|
set | Regulation of gene expression in endocrine-committed (NEUROG3+) progenitor cells |
setSize | 5 |
pANOVA | 0.0799 |
s.dist | 0.452 |
p.adjustANOVA | 0.44 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
NKX2-2 | 8967 |
NEUROG3 | 8818 |
PAX4 | 8018 |
INSM1 | 2173 |
NEUROD1 | -151 |
GeneID | Gene Rank |
---|---|
NKX2-2 | 8967 |
NEUROG3 | 8818 |
PAX4 | 8018 |
INSM1 | 2173 |
NEUROD1 | -151 |
Miscellaneous substrates
971 | |
---|---|
set | Miscellaneous substrates |
setSize | 12 |
pANOVA | 0.00746 |
s.dist | 0.446 |
p.adjustANOVA | 0.165 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CYP4F2 | 11778 |
CYP4B1 | 11439 |
CYP4F3 | 10723 |
CYP4F22 | 10494 |
CYP4F11 | 10463 |
CYP4A11 | 8201 |
CYP2D6 | 7364 |
CYP3A43 | 4152 |
CYP2U1 | 3356 |
CYP4A22 | 1397 |
CYP2S1 | -3035 |
CYP2W1 | -10428 |
GeneID | Gene Rank |
---|---|
CYP4F2 | 11778 |
CYP4B1 | 11439 |
CYP4F3 | 10723 |
CYP4F22 | 10494 |
CYP4F11 | 10463 |
CYP4A11 | 8201 |
CYP2D6 | 7364 |
CYP3A43 | 4152 |
CYP2U1 | 3356 |
CYP4A22 | 1397 |
CYP2S1 | -3035 |
CYP2W1 | -10428 |
CDC6 association with the ORC:origin complex
196 | |
---|---|
set | CDC6 association with the ORC:origin complex |
setSize | 8 |
pANOVA | 0.0295 |
s.dist | 0.444 |
p.adjustANOVA | 0.297 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
ORC1 | 9482 |
ORC4 | 9117 |
MCM8 | 7131 |
ORC6 | 7057 |
ORC3 | 6686 |
CDC6 | 2693 |
ORC5 | 1579 |
ORC2 | 56 |
GeneID | Gene Rank |
---|---|
ORC1 | 9482 |
ORC4 | 9117 |
MCM8 | 7131 |
ORC6 | 7057 |
ORC3 | 6686 |
CDC6 | 2693 |
ORC5 | 1579 |
ORC2 | 56 |
Defensins
405 | |
---|---|
set | Defensins |
setSize | 35 |
pANOVA | 5.74e-06 |
s.dist | 0.443 |
p.adjustANOVA | 0.00193 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CCR2 | 11662.0 |
DEFB133 | 11599.0 |
DEFB113 | 11464.0 |
DEFB116 | 11371.0 |
DEFB119 | 11287.0 |
DEFB118 | 11237.0 |
DEFB114 | 11213.0 |
DEFA4 | 11146.0 |
DEFB103A | 11037.5 |
DEFA5 | 10992.0 |
DEFA1 | 10974.0 |
DEFA3 | 10974.0 |
DEFB121 | 10678.0 |
TLR1 | 10582.0 |
DEFB135 | 10406.0 |
DEFA6 | 10402.0 |
DEFB136 | 10072.0 |
DEFB124 | 9944.0 |
DEFB123 | 7664.0 |
CCR6 | 6450.0 |
GeneID | Gene Rank |
---|---|
CCR2 | 11662.0 |
DEFB133 | 11599.0 |
DEFB113 | 11464.0 |
DEFB116 | 11371.0 |
DEFB119 | 11287.0 |
DEFB118 | 11237.0 |
DEFB114 | 11213.0 |
DEFA4 | 11146.0 |
DEFB103A | 11037.5 |
DEFA5 | 10992.0 |
DEFA1 | 10974.0 |
DEFA3 | 10974.0 |
DEFB121 | 10678.0 |
TLR1 | 10582.0 |
DEFB135 | 10406.0 |
DEFA6 | 10402.0 |
DEFB136 | 10072.0 |
DEFB124 | 9944.0 |
DEFB123 | 7664.0 |
CCR6 | 6450.0 |
DEFB115 | 6231.0 |
DEFB125 | 5903.0 |
DEFB126 | 4995.0 |
DEFB128 | 2190.0 |
DEFB127 | 1288.0 |
DEFB108B | 239.0 |
DEFB132 | -276.0 |
DEFB129 | -1733.0 |
DEFB104A | -3835.5 |
PRSS3 | -3921.0 |
DEFB1 | -4158.0 |
TLR2 | -5282.0 |
DEFB134 | -5459.0 |
ART1 | -7974.0 |
CD4 | -8591.0 |
Uptake and function of diphtheria toxin
1927 | |
---|---|
set | Uptake and function of diphtheria toxin |
setSize | 6 |
pANOVA | 0.065 |
s.dist | -0.435 |
p.adjustANOVA | 0.402 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CD9 | -9992 |
EEF2 | -9454 |
HSP90AB1 | -6678 |
TXNRD1 | -2247 |
HBEGF | -1421 |
HSP90AA1 | 1893 |
GeneID | Gene Rank |
---|---|
CD9 | -9992 |
EEF2 | -9454 |
HSP90AB1 | -6678 |
TXNRD1 | -2247 |
HBEGF | -1421 |
HSP90AA1 | 1893 |
Ciprofloxacin ADME
280 | |
---|---|
set | Ciprofloxacin ADME |
setSize | 5 |
pANOVA | 0.092 |
s.dist | 0.435 |
p.adjustANOVA | 0.463 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
ALB | 10551 |
SLCO1A2 | 10467 |
SLC22A8 | 6063 |
ABCG2 | 5581 |
SLC22A1 | -5827 |
GeneID | Gene Rank |
---|---|
ALB | 10551 |
SLCO1A2 | 10467 |
SLC22A8 | 6063 |
ABCG2 | 5581 |
SLC22A1 | -5827 |
GAB1 signalosome
639 | |
---|---|
set | GAB1 signalosome |
setSize | 17 |
pANOVA | 0.00191 |
s.dist | -0.435 |
p.adjustANOVA | 0.0951 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
EPGN | -10955 |
AREG | -10924 |
PIK3R1 | -10856 |
CSK | -10256 |
SRC | -9773 |
EREG | -9691 |
PXN | -8910 |
BTC | -6076 |
EGFR | -3464 |
EGF | -3037 |
GRB2 | -2663 |
HBEGF | -1421 |
TGFA | 1329 |
PIK3CA | 1513 |
PTPN11 | 1886 |
GAB1 | 1931 |
PAG1 | 2413 |
GeneID | Gene Rank |
---|---|
EPGN | -10955 |
AREG | -10924 |
PIK3R1 | -10856 |
CSK | -10256 |
SRC | -9773 |
EREG | -9691 |
PXN | -8910 |
BTC | -6076 |
EGFR | -3464 |
EGF | -3037 |
GRB2 | -2663 |
HBEGF | -1421 |
TGFA | 1329 |
PIK3CA | 1513 |
PTPN11 | 1886 |
GAB1 | 1931 |
PAG1 | 2413 |
Synthesis of Ketone Bodies
1737 | |
---|---|
set | Synthesis of Ketone Bodies |
setSize | 8 |
pANOVA | 0.0347 |
s.dist | -0.431 |
p.adjustANOVA | 0.326 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
HMGCS2 | -9396 |
HMGCL | -7839 |
AACS | -7611 |
BDH1 | -4744 |
HMGCLL1 | -2867 |
BDH2 | -2829 |
ACAT1 | -1028 |
ACSS3 | -533 |
GeneID | Gene Rank |
---|---|
HMGCS2 | -9396 |
HMGCL | -7839 |
AACS | -7611 |
BDH1 | -4744 |
HMGCLL1 | -2867 |
BDH2 | -2829 |
ACAT1 | -1028 |
ACSS3 | -533 |
Arachidonate production from DAG
127 | |
---|---|
set | Arachidonate production from DAG |
setSize | 5 |
pANOVA | 0.095 |
s.dist | -0.431 |
p.adjustANOVA | 0.469 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
DAGLA | -9279 |
ABHD12 | -6643 |
MGLL | -3948 |
DAGLB | -1920 |
ABHD6 | -1237 |
GeneID | Gene Rank |
---|---|
DAGLA | -9279 |
ABHD12 | -6643 |
MGLL | -3948 |
DAGLB | -1920 |
ABHD6 | -1237 |
Nef Mediated CD8 Down-regulation
1056 | |
---|---|
set | Nef Mediated CD8 Down-regulation |
setSize | 7 |
pANOVA | 0.0512 |
s.dist | -0.426 |
p.adjustANOVA | 0.379 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
AP2A2 | -10138 |
AP2M1 | -7849 |
AP2A1 | -6828 |
AP2S1 | -5603 |
CD8B | -4309 |
AP2B1 | -672 |
ATP6V1H | 3615 |
GeneID | Gene Rank |
---|---|
AP2A2 | -10138 |
AP2M1 | -7849 |
AP2A1 | -6828 |
AP2S1 | -5603 |
CD8B | -4309 |
AP2B1 | -672 |
ATP6V1H | 3615 |
Specification of the neural plate border
1710 | |
---|---|
set | Specification of the neural plate border |
setSize | 16 |
pANOVA | 0.00343 |
s.dist | 0.422 |
p.adjustANOVA | 0.103 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
ZIC1 | 11564 |
GBX2 | 9673 |
TFAP2B | 9377 |
MSX1 | 8393 |
PAX3 | 8375 |
WNT3A | 8366 |
SOX2 | 7488 |
PAX7 | 7272 |
DLX5 | 6973 |
BMP4 | 6751 |
FGF4 | 3879 |
TFAP2C | 3854 |
MYB | 3783 |
CTNNB1 | -333 |
TCF7L1 | -1676 |
TFAP2A | -10219 |
GeneID | Gene Rank |
---|---|
ZIC1 | 11564 |
GBX2 | 9673 |
TFAP2B | 9377 |
MSX1 | 8393 |
PAX3 | 8375 |
WNT3A | 8366 |
SOX2 | 7488 |
PAX7 | 7272 |
DLX5 | 6973 |
BMP4 | 6751 |
FGF4 | 3879 |
TFAP2C | 3854 |
MYB | 3783 |
CTNNB1 | -333 |
TCF7L1 | -1676 |
TFAP2A | -10219 |
Antimicrobial peptides
118 | |
---|---|
set | Antimicrobial peptides |
setSize | 79 |
pANOVA | 9.67e-11 |
s.dist | 0.421 |
p.adjustANOVA | 4.86e-08 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
HTN1 | 11815.0 |
ITLN1 | 11712.0 |
S100A7 | 11670.0 |
CCR2 | 11662.0 |
DEFB133 | 11599.0 |
HTN3 | 11582.0 |
LYZ | 11557.0 |
RNASE6 | 11547.0 |
DEFB113 | 11464.0 |
DEFB116 | 11371.0 |
DEFB119 | 11287.0 |
REG3G | 11240.0 |
DEFB118 | 11237.0 |
DEFB114 | 11213.0 |
DEFA4 | 11146.0 |
BPIFA1 | 11113.0 |
DEFB103A | 11037.5 |
DEFA5 | 10992.0 |
RNASE3 | 10988.0 |
DEFA1 | 10974.0 |
GeneID | Gene Rank |
---|---|
HTN1 | 11815.0 |
ITLN1 | 11712.0 |
S100A7 | 11670.0 |
CCR2 | 11662.0 |
DEFB133 | 11599.0 |
HTN3 | 11582.0 |
LYZ | 11557.0 |
RNASE6 | 11547.0 |
DEFB113 | 11464.0 |
DEFB116 | 11371.0 |
DEFB119 | 11287.0 |
REG3G | 11240.0 |
DEFB118 | 11237.0 |
DEFB114 | 11213.0 |
DEFA4 | 11146.0 |
BPIFA1 | 11113.0 |
DEFB103A | 11037.5 |
DEFA5 | 10992.0 |
RNASE3 | 10988.0 |
DEFA1 | 10974.0 |
DEFA3 | 10974.0 |
PDZD11 | 10739.0 |
S100A8 | 10710.0 |
DEFB121 | 10678.0 |
CHGA | 10641.0 |
DCD | 10629.0 |
PGLYRP4 | 10624.0 |
TLR1 | 10582.0 |
PGLYRP3 | 10550.0 |
BPIFB6 | 10523.0 |
S100A7A | 10474.0 |
DEFB135 | 10406.0 |
DEFA6 | 10402.0 |
REG3A | 10292.0 |
BPIFA2 | 10225.0 |
DEFB136 | 10072.0 |
DEFB124 | 9944.0 |
EPPIN | 9831.0 |
CTSG | 9320.0 |
PRTN3 | 8475.0 |
BPI | 8243.0 |
DEFB123 | 7664.0 |
BPIFB1 | 6987.0 |
CCR6 | 6450.0 |
DEFB115 | 6231.0 |
LTF | 6135.0 |
DEFB125 | 5903.0 |
BPIFB4 | 5329.0 |
DEFB126 | 4995.0 |
PLA2G2A | 2552.0 |
DEFB128 | 2190.0 |
PGLYRP2 | 2050.0 |
DEFB127 | 1288.0 |
ATOX1 | 903.0 |
ATP7A | 660.0 |
GNLY | 659.0 |
DEFB108B | 239.0 |
SEMG1 | -57.0 |
DEFB132 | -276.0 |
S100A9 | -848.0 |
ELANE | -917.0 |
CAMP | -921.0 |
PI3 | -978.0 |
BPIFB2 | -1070.0 |
SLC11A1 | -1730.0 |
DEFB129 | -1733.0 |
CLU | -2655.0 |
PGLYRP1 | -3622.0 |
DEFB104A | -3835.5 |
PRSS3 | -3921.0 |
DEFB1 | -4158.0 |
TLR2 | -5282.0 |
DEFB134 | -5459.0 |
RNASE8 | -7176.0 |
ART1 | -7974.0 |
CD4 | -8591.0 |
RNASE7 | -9821.0 |
LCN2 | -10144.0 |
LEAP2 | -10658.0 |
CLEC7A/inflammasome pathway
202 | |
---|---|
set | CLEC7A/inflammasome pathway |
setSize | 6 |
pANOVA | 0.0761 |
s.dist | -0.418 |
p.adjustANOVA | 0.431 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
PYCARD | -9180 |
CASP8 | -7685 |
RELA | -5693 |
NFKB1 | -3083 |
IL1B | -1477 |
MALT1 | 383 |
GeneID | Gene Rank |
---|---|
PYCARD | -9180 |
CASP8 | -7685 |
RELA | -5693 |
NFKB1 | -3083 |
IL1B | -1477 |
MALT1 | 383 |
Activation of the phototransduction cascade
81 | |
---|---|
set | Activation of the phototransduction cascade |
setSize | 11 |
pANOVA | 0.017 |
s.dist | -0.416 |
p.adjustANOVA | 0.236 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
PDE6G | -9397 |
GNB1 | -9151 |
PDE6B | -9103 |
PDE6A | -8612 |
GNAT1 | -7039 |
GNGT1 | -6465 |
RHO | -4695 |
CNGB1 | -3831 |
SAG | -2722 |
SLC24A1 | 1128 |
CNGA1 | 11199 |
GeneID | Gene Rank |
---|---|
PDE6G | -9397 |
GNB1 | -9151 |
PDE6B | -9103 |
PDE6A | -8612 |
GNAT1 | -7039 |
GNGT1 | -6465 |
RHO | -4695 |
CNGB1 | -3831 |
SAG | -2722 |
SLC24A1 | 1128 |
CNGA1 | 11199 |
Epithelial-Mesenchymal Transition (EMT) during gastrulation
510 | |
---|---|
set | Epithelial-Mesenchymal Transition (EMT) during gastrulation |
setSize | 7 |
pANOVA | 0.0602 |
s.dist | -0.41 |
p.adjustANOVA | 0.39 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CLDN7 | -10994 |
OCLN | -9111 |
CDH1 | -8854 |
FGFR1 | -7705 |
EOMES | -3817 |
TBXT | 2986 |
SNAI1 | 6954 |
GeneID | Gene Rank |
---|---|
CLDN7 | -10994 |
OCLN | -9111 |
CDH1 | -8854 |
FGFR1 | -7705 |
EOMES | -3817 |
TBXT | 2986 |
SNAI1 | 6954 |
Reversible hydration of carbon dioxide
1506 | |
---|---|
set | Reversible hydration of carbon dioxide |
setSize | 12 |
pANOVA | 0.015 |
s.dist | -0.406 |
p.adjustANOVA | 0.223 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
CA6 | -10654 |
CA14 | -10384 |
CA12 | -9769 |
CA9 | -8734 |
CA5B | -7239 |
CA3 | -7158 |
CA7 | -4715 |
CA5A | -1370 |
CA2 | -519 |
CA4 | -28 |
CA1 | -27 |
CA13 | 8883 |
GeneID | Gene Rank |
---|---|
CA6 | -10654 |
CA14 | -10384 |
CA12 | -9769 |
CA9 | -8734 |
CA5B | -7239 |
CA3 | -7158 |
CA7 | -4715 |
CA5A | -1370 |
CA2 | -519 |
CA4 | -28 |
CA1 | -27 |
CA13 | 8883 |
Loss of MECP2 binding ability to the NCoR/SMRT complex
890 | |
---|---|
set | Loss of MECP2 binding ability to the NCoR/SMRT complex |
setSize | 7 |
pANOVA | 0.0686 |
s.dist | -0.398 |
p.adjustANOVA | 0.408 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
NCOR2 | -9391 |
GPS2 | -8479 |
MECP2 | -7871 |
HDAC3 | -3920 |
TBL1XR1 | -3347 |
TBL1X | -1788 |
NCOR1 | 5273 |
GeneID | Gene Rank |
---|---|
NCOR2 | -9391 |
GPS2 | -8479 |
MECP2 | -7871 |
HDAC3 | -3920 |
TBL1XR1 | -3347 |
TBL1X | -1788 |
NCOR1 | 5273 |
Negative feedback regulation of MAPK pathway
1061 | |
---|---|
set | Negative feedback regulation of MAPK pathway |
setSize | 6 |
pANOVA | 0.0922 |
s.dist | -0.397 |
p.adjustANOVA | 0.463 |
Top
enriched genes
GeneID | Gene Rank |
---|---|
MAP2K2 | -10683 |
BRAF | -6923 |
MAPK1 | -6543 |
MAPK3 | -2855 |
MAP2K1 | 785 |
RAF1 | 948 |
GeneID | Gene Rank |
---|---|
MAP2K2 | -10683 |
BRAF | -6923 |
MAPK1 | -6543 |
MAPK3 | -2855 |
MAP2K1 | 785 |
RAF1 | 948 |
Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.3.2 (2023-10-31)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 22.04.3 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/openblas-pthread/libblas.so.3
## LAPACK: /usr/lib/x86_64-linux-gnu/openblas-pthread/libopenblasp-r0.3.20.so; LAPACK version 3.10.0
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## time zone: Etc/UTC
## tzcode source: system (glibc)
##
## attached base packages:
## [1] parallel stats4 stats graphics grDevices utils datasets
## [8] methods base
##
## other attached packages:
## [1] pkgload_1.3.3
## [2] GGally_2.2.0
## [3] ggplot2_3.4.4
## [4] reshape2_1.4.4
## [5] gplots_3.1.3
## [6] gtools_3.9.5
## [7] tibble_3.2.1
## [8] dplyr_1.1.4
## [9] echarts4r_0.4.5
## [10] png_0.1-8
## [11] gridExtra_2.3
## [12] missMethyl_1.36.0
## [13] beeswarm_0.4.0
## [14] kableExtra_1.3.4
## [15] tictoc_1.2
## [16] HGNChelper_0.8.1
## [17] IlluminaHumanMethylationEPICanno.ilm10b4.hg19_0.6.0
## [18] IlluminaHumanMethylation450kanno.ilmn12.hg19_0.6.1
## [19] minfi_1.48.0
## [20] bumphunter_1.44.0
## [21] locfit_1.5-9.8
## [22] iterators_1.0.14
## [23] foreach_1.5.2
## [24] Biostrings_2.70.1
## [25] XVector_0.42.0
## [26] SummarizedExperiment_1.32.0
## [27] Biobase_2.62.0
## [28] MatrixGenerics_1.14.0
## [29] matrixStats_1.2.0
## [30] GenomicRanges_1.54.1
## [31] GenomeInfoDb_1.38.2
## [32] IRanges_2.36.0
## [33] S4Vectors_0.40.2
## [34] BiocGenerics_0.48.1
## [35] eulerr_7.0.0
## [36] limma_3.58.1
## [37] mitch_1.15.2
##
## loaded via a namespace (and not attached):
## [1] splines_4.3.2 later_1.3.2
## [3] BiocIO_1.12.0 bitops_1.0-7
## [5] filelock_1.0.3 preprocessCore_1.64.0
## [7] XML_3.99-0.16 lifecycle_1.0.4
## [9] lattice_0.22-5 MASS_7.3-60
## [11] base64_2.0.1 scrime_1.3.5
## [13] magrittr_2.0.3 sass_0.4.8
## [15] rmarkdown_2.25 jquerylib_0.1.4
## [17] yaml_2.3.8 httpuv_1.6.13
## [19] askpass_1.2.0 doRNG_1.8.6
## [21] DBI_1.1.3 RColorBrewer_1.1-3
## [23] abind_1.4-5 zlibbioc_1.48.0
## [25] quadprog_1.5-8 rvest_1.0.3
## [27] purrr_1.0.2 RCurl_1.98-1.13
## [29] rappdirs_0.3.3 GenomeInfoDbData_1.2.11
## [31] genefilter_1.84.0 annotate_1.80.0
## [33] svglite_2.1.3 DelayedMatrixStats_1.24.0
## [35] codetools_0.2-19 DelayedArray_0.28.0
## [37] xml2_1.3.6 tidyselect_1.2.0
## [39] beanplot_1.3.1 BiocFileCache_2.10.1
## [41] illuminaio_0.44.0 webshot_0.5.5
## [43] GenomicAlignments_1.38.0 jsonlite_1.8.8
## [45] multtest_2.58.0 ellipsis_0.3.2
## [47] survival_3.5-7 systemfonts_1.0.5
## [49] tools_4.3.2 progress_1.2.3
## [51] Rcpp_1.0.11 glue_1.6.2
## [53] SparseArray_1.2.2 xfun_0.41
## [55] HDF5Array_1.30.0 withr_2.5.2
## [57] fastmap_1.1.1 rhdf5filters_1.14.1
## [59] fansi_1.0.6 openssl_2.1.1
## [61] caTools_1.18.2 digest_0.6.33
## [63] R6_2.5.1 mime_0.12
## [65] colorspace_2.1-0 biomaRt_2.58.0
## [67] RSQLite_2.3.4 utf8_1.2.4
## [69] tidyr_1.3.0 generics_0.1.3
## [71] data.table_1.14.10 rtracklayer_1.62.0
## [73] prettyunits_1.2.0 httr_1.4.7
## [75] htmlwidgets_1.6.4 S4Arrays_1.2.0
## [77] ggstats_0.5.1 pkgconfig_2.0.3
## [79] gtable_0.3.4 blob_1.2.4
## [81] siggenes_1.76.0 htmltools_0.5.7
## [83] scales_1.3.0 knitr_1.45
## [85] rstudioapi_0.15.0 tzdb_0.4.0
## [87] rjson_0.2.21 nlme_3.1-163
## [89] curl_5.2.0 org.Hs.eg.db_3.18.0
## [91] cachem_1.0.8 rhdf5_2.46.1
## [93] stringr_1.5.1 KernSmooth_2.23-22
## [95] AnnotationDbi_1.64.1 restfulr_0.0.15
## [97] GEOquery_2.70.0 pillar_1.9.0
## [99] grid_4.3.2 reshape_0.8.9
## [101] vctrs_0.6.5 promises_1.2.1
## [103] dbplyr_2.4.0 xtable_1.8-4
## [105] evaluate_0.23 readr_2.1.4
## [107] GenomicFeatures_1.54.1 cli_3.6.2
## [109] compiler_4.3.2 Rsamtools_2.18.0
## [111] rlang_1.1.2 crayon_1.5.2
## [113] rngtools_1.5.2 nor1mix_1.3-2
## [115] mclust_6.0.1 plyr_1.8.9
## [117] stringi_1.8.3 viridisLite_0.4.2
## [119] BiocParallel_1.36.0 munsell_0.5.0
## [121] Matrix_1.6-1.1 hms_1.1.3
## [123] sparseMatrixStats_1.14.0 bit64_4.0.5
## [125] Rhdf5lib_1.24.1 KEGGREST_1.42.0
## [127] statmod_1.5.0 shiny_1.8.0
## [129] highr_0.10 memoise_2.0.1
## [131] bslib_0.6.1 bit_4.0.5
END of report