Complement and Coagulation Cascades(Mus musculus)

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Results for "Complement and Coagulation Cascades(Mus musculus)": 1001 gene sets

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Complement and Coagulation Cascades(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Complement and Coagulation Cascades(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
complement and coagulation cascades Gene Set From KEGG Pathways proteins participating in the complement and coagulation cascades pathway from the KEGG Pathways dataset.
Complement and Coagulation Cascades(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Complement and Coagulation Cascades(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Dengue 2 interactions with complement and coagulation cascades Gene Set From WikiPathways Pathways 2024 proteins participating in the Dengue 2 interactions with complement and coagulation cascades pathway from the WikiPathways Pathways 2024 dataset.
Complement and coagulation cascades Gene Set From WikiPathways Pathways 2024 proteins participating in the Complement and coagulation cascades pathway from the WikiPathways Pathways 2024 dataset.
Complement and coagulation cascades Gene Set From KEGG Pathways 2026 proteins participating in the Complement and coagulation cascades pathway from the KEGG Pathways 2026 dataset.
Complement Activation, Classical Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Complement Activation, Classical Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Glycolysis and Gluconeogenesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Glycolysis and Gluconeogenesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Glutathione and one carbon metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Glutathione and one carbon metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
One carbon metabolism and related pathways(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the One carbon metabolism and related pathways(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Serotonin and anxiety(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Serotonin and anxiety(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Synthesis and Degradation of Ketone Bodies(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Synthesis and Degradation of Ketone Bodies(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Prostaglandin Synthesis and Regulation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Prostaglandin Synthesis and Regulation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Cytokines and Inflammatory Response (BioCarta)(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Cytokines and Inflammatory Response (BioCarta)(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Alanine and aspartate metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Alanine and aspartate metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Serotonin and anxiety-related events(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Serotonin and anxiety-related events(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Leptin and adiponectin(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Leptin and adiponectin(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
FAS pathway and Stress induction of HSP regulation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the FAS pathway and Stress induction of HSP regulation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Myometrial Relaxation and Contraction Pathways(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Myometrial Relaxation and Contraction Pathways(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Wnt Signaling Pathway and Pluripotency(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Wnt Signaling Pathway and Pluripotency(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Nuclear receptors in lipid metabolism and toxicity(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Nuclear receptors in lipid metabolism and toxicity(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Mus musculus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Mus musculus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Regulation of Cardiac Hypertrophy by miR-208(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Regulation of Cardiac Hypertrophy by miR-208(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Chemokine signaling pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Chemokine signaling pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Hypertrophy Model(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Hypertrophy Model(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Peptide GPCRs(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Peptide GPCRs(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Apoptosis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Apoptosis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
GPCRs, Class B Secretin-like(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the GPCRs, Class B Secretin-like(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SIDS Susceptibility Pathways(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SIDS Susceptibility Pathways(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
miR-1 in cardiac development(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the miR-1 in cardiac development(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Biogenic Amine Synthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Biogenic Amine Synthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
G13 Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the G13 Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
ESC Pluripotency Pathways(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the ESC Pluripotency Pathways(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Triacylglyceride Synthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Triacylglyceride Synthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Histone modifications(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Histone modifications(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Mismatch repair(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Mismatch repair(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Ptf1a related regulatory pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Ptf1a related regulatory pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Id Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Id Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Cytoplasmic Ribosomal Proteins(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Cytoplasmic Ribosomal Proteins(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
IL-6 signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the IL-6 signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
G1 to S cell cycle control(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the G1 to S cell cycle control(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Pentose Phosphate Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Pentose Phosphate Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Signaling of Hepatocyte Growth Factor Receptor(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Signaling of Hepatocyte Growth Factor Receptor(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Folic Acid Network(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Folic Acid Network(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Methylation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Methylation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Non-odorant GPCRs(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Non-odorant GPCRs(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Amino acid conjugation of benzoic acid(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Amino acid conjugation of benzoic acid(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
EBV LMP1 signaling(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the EBV LMP1 signaling(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Hedgehog Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Hedgehog Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Proteasome Degradation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Proteasome Degradation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
MAPK signaling pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the MAPK signaling pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Spinal Cord Injury(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Spinal Cord Injury(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Heart Development(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Heart Development(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Selenium metabolism/Selenoproteins(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Selenium metabolism/Selenoproteins(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Leptin Insulin Overlap(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Leptin Insulin Overlap(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
IL-7 Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the IL-7 Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
EPO Receptor Signaling(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the EPO Receptor Signaling(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Glycogen Metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Glycogen Metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Mitochondrial Gene Expression(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Mitochondrial Gene Expression(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Adipogenesis genes(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Adipogenesis genes(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Fatty Acid Omega Oxidation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Fatty Acid Omega Oxidation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Oxidative Stress(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Oxidative Stress(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Polyol pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Polyol pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Mitochondrial LC-Fatty Acid Beta-Oxidation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Mitochondrial LC-Fatty Acid Beta-Oxidation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Ovarian Infertility Genes(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Ovarian Infertility Genes(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Calcium Regulation in the Cardiac Cell(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Calcium Regulation in the Cardiac Cell(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
ACE Inhibitor Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the ACE Inhibitor Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Small Ligand GPCRs(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Small Ligand GPCRs(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
miRNA regulation of DNA Damage Response(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the miRNA regulation of DNA Damage Response(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Kit Receptor Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Kit Receptor Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Acetylcholine Synthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Acetylcholine Synthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Endochondral Ossification(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Endochondral Ossification(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Glucocorticoid & Mineralcorticoid Metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Glucocorticoid & Mineralcorticoid Metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
PPAR signaling pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the PPAR signaling pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Estrogen signalling(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Estrogen signalling(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Cholesterol Biosynthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Cholesterol Biosynthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
mRNA processing(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the mRNA processing(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Diurnally Regulated Genes with Circadian Orthologs(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Diurnally Regulated Genes with Circadian Orthologs(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Delta-Notch Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Delta-Notch Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Fatty Acid Beta Oxidation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Fatty Acid Beta Oxidation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Splicing factor NOVA regulated synpatic proteins(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Splicing factor NOVA regulated synpatic proteins(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Striated Muscle Contraction(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Striated Muscle Contraction(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
IL-3 Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the IL-3 Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
G Protein Signaling Pathways(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the G Protein Signaling Pathways(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Osteoblast(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Osteoblast(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Arachidonate Epoxygenase Epoxide Hydrolase(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Arachidonate Epoxygenase Epoxide Hydrolase(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Irinotecan Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Irinotecan Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
IL-1 Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the IL-1 Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Insulin Signaling(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Insulin Signaling(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Oxidative phosphorylation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Oxidative phosphorylation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Hypothetical Network for Drug Addiction(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Hypothetical Network for Drug Addiction(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Odorant GPCRs(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Odorant GPCRs(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
DNA Replication(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the DNA Replication(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Retinol metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Retinol metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Regulation of Actin Cytoskeleton(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Regulation of Actin Cytoskeleton(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Estrogen metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Estrogen metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Nuclear Receptors(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Nuclear Receptors(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
PodNet: protein-protein interactions in the podocyte(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the PodNet: protein-protein interactions in the podocyte(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
TCA Cycle(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the TCA Cycle(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Heme Biosynthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Heme Biosynthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Fatty acid oxidation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Fatty acid oxidation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Selenium Micronutrient Network(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Selenium Micronutrient Network(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
IL-5 Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the IL-5 Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Blood Clotting Cascade(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Blood Clotting Cascade(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
One Carbon Metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the One Carbon Metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Non-homologous end joining(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Non-homologous end joining(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Matrix Metalloproteinases(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Matrix Metalloproteinases(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Metapathway biotransformation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Metapathway biotransformation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Integrin-mediated Cell Adhesion(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Integrin-mediated Cell Adhesion(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Glutathione metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Glutathione metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Homologous recombination(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Homologous recombination(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
MicroRNAs in Cardiomyocyte Hypertrophy(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the MicroRNAs in Cardiomyocyte Hypertrophy(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Translation Factors(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Translation Factors(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Macrophage markers(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Macrophage markers(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Aflatoxin B1 metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Aflatoxin B1 metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Eukaryotic Transcription Initiation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Eukaryotic Transcription Initiation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Iron Homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Iron Homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Phase I biontransformations, non P450(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Phase I biontransformations, non P450(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
TGF Beta Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the TGF Beta Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Electron Transport Chain(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Electron Transport Chain(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Alzheimers Disease(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Alzheimers Disease(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Wnt Signaling Pathway NetPath(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Wnt Signaling Pathway NetPath(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
EGFR1 Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the EGFR1 Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Glucuronidation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Glucuronidation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
ErbB signaling pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the ErbB signaling pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Kennedy pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Kennedy pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Amino Acid metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Amino Acid metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
GPCRs, Class C Metabotropic glutamate, pheromone(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the GPCRs, Class C Metabotropic glutamate, pheromone(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Toll Like Receptor signaling(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Toll Like Receptor signaling(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Osteoclast(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Osteoclast(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
NLR Proteins(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the NLR Proteins(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Statin Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Statin Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
TNF-alpha NF-kB Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the TNF-alpha NF-kB Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Keap1-Nrf2(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Keap1-Nrf2(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Signal Transduction of S1P Receptor(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Signal Transduction of S1P Receptor(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
p38 MAPK Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the p38 MAPK Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Apoptosis Modulation by HSP70(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Apoptosis Modulation by HSP70(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Inflammatory Response Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Inflammatory Response Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Notch Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Notch Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Dopminergic Neurogenesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Dopminergic Neurogenesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
XPodNet - protein-protein interactions in the podocyte expanded by STRING(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the XPodNet - protein-protein interactions in the podocyte expanded by STRING(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Neural retinal development(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Neural retinal development(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Exercise-induced Circadian Regulation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Exercise-induced Circadian Regulation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
GPCRs, Other(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the GPCRs, Other(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
PluriNetWork(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the PluriNetWork(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
GPCRs, Class A Rhodopsin-like(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the GPCRs, Class A Rhodopsin-like(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Type II interferon signaling (IFNG)(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Type II interferon signaling (IFNG)(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Focal Adhesion(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Focal Adhesion(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Tryptophan metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Tryptophan metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Steroid Biosynthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Steroid Biosynthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Alpha6-Beta4 Integrin Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Alpha6-Beta4 Integrin Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Wnt Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Wnt Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Purine metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Purine metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Orphan GPCRs(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Orphan GPCRs(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Monoamine GPCRs(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Monoamine GPCRs(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Eicosanoid Synthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Eicosanoid Synthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Nucleotide Metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Nucleotide Metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Oxidative Damage(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Oxidative Damage(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Oxidation by Cytochrome P450(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Oxidation by Cytochrome P450(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Nucleotide GPCRs(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Nucleotide GPCRs(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
MAPK Cascade(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the MAPK Cascade(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Fatty Acid Biosynthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Fatty Acid Biosynthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
IL-9 Signaling Pathway(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the IL-9 Signaling Pathway(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cascades Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cascades in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cascades Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term cascades in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Toll-Like Receptors Cascades Gene Set From Reactome Pathways 2014 proteins participating in the Toll-Like Receptors Cascades pathway from the Reactome Pathways dataset.
MAPK family signaling cascades Gene Set From Reactome Pathways 2024 proteins participating in the MAPK family signaling cascades pathway from the Reactome Pathways 2024 dataset.
Toll-like Receptor Cascades Gene Set From Reactome Pathways 2024 proteins participating in the Toll-like Receptor Cascades pathway from the Reactome Pathways 2024 dataset.
Complement C3 and C4 levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Complement C3 and C4 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Complement Hyperactivation, Angiopathic Thrombosis, And Protein-Losing Enteropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complement Hyperactivation, Angiopathic Thrombosis, And Protein-Losing Enteropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complement system in neuronal development and plasticity Gene Set From WikiPathways Pathways 2024 proteins participating in the Complement system in neuronal development and plasticity pathway from the WikiPathways Pathways 2024 dataset.
Complement C3 and C4 levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complement C3 and C4 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
musculus Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term musculus in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
mus Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term mus in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
protein c inhibitor-coagulation factor xa complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the protein c inhibitor-coagulation factor xa complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
protein c inhibitor-coagulation factor xi complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the protein c inhibitor-coagulation factor xi complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
protein c inhibitor-coagulation factor v complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the protein c inhibitor-coagulation factor v complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset.
Blood Coagulation Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Blood Coagulation Disorders from the curated CTD Gene-Disease Associations dataset.
Blood Coagulation Disorders, Inherited Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Blood Coagulation Disorders, Inherited from the curated CTD Gene-Disease Associations dataset.
Disseminated Intravascular Coagulation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Disseminated Intravascular Coagulation from the curated CTD Gene-Disease Associations dataset.
Blood Coagulation Factors Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Blood Coagulation Factors in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Blood Coagulation Factor Inhibitors Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Blood Coagulation Factor Inhibitors in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
blood coagulation disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease blood coagulation disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
inherited blood coagulation disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease inherited blood coagulation disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
disseminated intravascular coagulation Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease disseminated intravascular coagulation in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
blood coagulation disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease blood coagulation disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
inherited blood coagulation disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inherited blood coagulation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
disseminated intravascular coagulation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease disseminated intravascular coagulation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
blood coagulation disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease blood coagulation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
Coagulation Factor IX Gene Set From DrugBank Drug Targets interacting proteins for the Coagulation Factor IX drug from the curated DrugBank Drug Targets dataset.
Coagulation factor VIIa Gene Set From DrugBank Drug Targets interacting proteins for the Coagulation factor VIIa drug from the curated DrugBank Drug Targets dataset.
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
deficiency of coagulation factor v Gene Set From GAD Gene-Disease Associations genes associated with the disease deficiency of coagulation factor v in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercholesterolemia; h. pylori infection; coagulation disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercholesterolemia; h. pylori infection; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation factors Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; inflammation; nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; inflammation; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy loss, recurrent; coagulation disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; osteonecrosis; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; osteonecrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
plasma coagulation factors Gene Set From GAD Gene-Disease Associations genes associated with the disease plasma coagulation factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation factor inhibitors Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation factor inhibitors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coagulation disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
triglycerides; coagulation factor vii; phospolipids Gene Set From GAD Gene-Disease Associations genes associated with the disease triglycerides; coagulation factor vii; phospolipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coagulation protein disorders; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coagulation protein disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; acute disease; disseminated intravascular coagulation; poisoning Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; acute disease; disseminated intravascular coagulation; poisoning in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; legg-perthes disease; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ulcer, gastric; repaglinide pharmacology; coagulation disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease ulcer, gastric; repaglinide pharmacology; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disseminated intravascular coagulation; meningococcal infections Gene Set From GAD Gene-Disease Associations genes associated with the disease disseminated intravascular coagulation; meningococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coagulation Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term coagulation in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
regulation of blood coagulation, intrinsic pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of blood coagulation, intrinsic pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of blood coagulation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of blood coagulation biological process from the curated GO Biological Process Annotations 2015 dataset.
coagulation Gene Set From GO Biological Process Annotations 2015 genes participating in the coagulation biological process from the curated GO Biological Process Annotations 2015 dataset.
blood coagulation, extrinsic pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the blood coagulation, extrinsic pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of coagulation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of coagulation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of coagulation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of coagulation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of coagulation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of coagulation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of blood coagulation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of blood coagulation biological process from the curated GO Biological Process Annotations 2015 dataset.
blood coagulation Gene Set From GO Biological Process Annotations 2015 genes participating in the blood coagulation biological process from the curated GO Biological Process Annotations 2015 dataset.
blood coagulation, intrinsic pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the blood coagulation, intrinsic pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
activation of blood coagulation via clotting cascade Gene Set From GO Biological Process Annotations 2015 genes participating in the activation of blood coagulation via clotting cascade biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of blood coagulation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of blood coagulation biological process from the curated GO Biological Process Annotations 2015 dataset.
blood coagulation, common pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the blood coagulation, common pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
protein c inhibitor-coagulation factor xa complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the protein c inhibitor-coagulation factor xa complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
protein c inhibitor-coagulation factor xi complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the protein c inhibitor-coagulation factor xi complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
protein c inhibitor-coagulation factor v complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the protein c inhibitor-coagulation factor v complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
Coagulation factor levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Coagulation factor levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
End-stage coagulation Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the End-stage coagulation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
blood coagulation disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease blood coagulation disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
inherited blood coagulation disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease inherited blood coagulation disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of the common coagulation pathway Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the coagulation cascade Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coagulation cascade phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of coagulation Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of coagulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the coagulation cascade Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the coagulation cascade phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
disseminated intravascular coagulation Gene Set From HPO Gene-Disease Associations genes associated with the disseminated intravascular coagulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the common coagulation pathway Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the common coagulation pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of coagulation Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of coagulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Coagulation Protein Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Coagulation Protein Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Disseminated Intravascular Coagulation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Disseminated Intravascular Coagulation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Blood Coagulation Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Blood Coagulation Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Blood Coagulation Disorders, Inherited Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Blood Coagulation Disorders, Inherited phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Tissue factor/coagulation factor III Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tissue factor/coagulation factor III protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Coagulation factor V Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Coagulation factor V protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Coagulation factor 8 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Coagulation factor 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Peptidase S1A, coagulation factor VII/IX/X/C/Z Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase S1A, coagulation factor VII/IX/X/C/Z protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Coagulation factor 5/8 C-terminal type domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Coagulation factor 5/8 C-terminal type domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Coagulation factor 5/8 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Coagulation factor 5/8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Coagulation factor, subgroup, Gla domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Coagulation factor, subgroup, Gla domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Blood coagulation inhibitor, Disintegrin Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Blood coagulation inhibitor, Disintegrin protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Coagulation factor XIIa/hepatocyte growth factor activator Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Coagulation factor XIIa/hepatocyte growth factor activator protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal blood coagulation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal blood coagulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
Blood coagulation Gene Set From PANTHER Pathways proteins participating in the Blood coagulation pathway from the PANTHER Pathways dataset.
Disseminated Intravascular Coagulation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disseminated Intravascular Coagulation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Disseminated Intravascular Coagulation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Disseminated Intravascular Coagulation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Body Skin Hyperlaxity Due To Vitamin K Dependent Coagulation Factor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Body Skin Hyperlaxity Due To Vitamin K Dependent Coagulation Factor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Coagulation Factor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Coagulation Factor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Specified Coagulation Defects Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Coagulation Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Coagulation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Coagulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Coagulation Factor Measurement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Coagulation Factor Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Elevated Coagulation Factor V Activity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Coagulation Factor V Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
blood coagulation, fibrin clot formation Gene Set From GO Biological Process Annotations 2023 genes participating in the blood coagulation, fibrin clot formation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of blood coagulation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of blood coagulation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of blood coagulation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of blood coagulation biological process from the curated GO Biological Process Annotations 2023 dataset.
blood coagulation, intrinsic pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the blood coagulation, intrinsic pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of blood coagulation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of blood coagulation biological process from the curated GO Biological Process Annotations 2023 dataset.
blood coagulation, common pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the blood coagulation, common pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of coagulation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of coagulation biological process from the curated GO Biological Process Annotations 2023 dataset.
activation of blood coagulation via clotting cascade Gene Set From GO Biological Process Annotations 2023 genes participating in the activation of blood coagulation via clotting cascade biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of coagulation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of coagulation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of coagulation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of coagulation biological process from the curated GO Biological Process Annotations 2023 dataset.
protein C inhibitor-coagulation factor V complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the protein C inhibitor-coagulation factor V complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
protein C inhibitor-coagulation factor Xa complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the protein C inhibitor-coagulation factor Xa complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
protein C inhibitor-coagulation factor XI complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the protein C inhibitor-coagulation factor XI complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
abnormal blood coagulation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood coagulation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired blood coagulation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired blood coagulation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
positive regulation of coagulation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of coagulation biological process from the curated GO Biological Process Annotations 2025 dataset.
blood coagulation, fibrin clot formation Gene Set From GO Biological Process Annotations 2025 genes participating in the blood coagulation, fibrin clot formation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of blood coagulation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of blood coagulation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of blood coagulation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of blood coagulation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of blood coagulation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of blood coagulation biological process from the curated GO Biological Process Annotations 2025 dataset.
blood coagulation, intrinsic pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the blood coagulation, intrinsic pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
blood coagulation, common pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the blood coagulation, common pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of blood coagulation, common pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of blood coagulation, common pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of coagulation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of coagulation biological process from the curated GO Biological Process Annotations 2025 dataset.
activation of blood coagulation via clotting cascade Gene Set From GO Biological Process Annotations 2025 genes participating in the activation of blood coagulation via clotting cascade biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of coagulation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of coagulation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of blood coagulation, common pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of blood coagulation, common pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
protein C inhibitor-coagulation factor V complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the protein C inhibitor-coagulation factor V complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
protein C inhibitor-coagulation factor Xa complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the protein C inhibitor-coagulation factor Xa complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
protein C inhibitor-coagulation factor XI complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the protein C inhibitor-coagulation factor XI complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Blood coagulation disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Blood coagulation disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Blood coagulation disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Blood coagulation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Disseminated intravascular coagulation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Disseminated intravascular coagulation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Protein C inhibitor-coagulation factor V complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Protein C inhibitor-coagulation factor V complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Protein C inhibitor-coagulation factor Xa complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Protein C inhibitor-coagulation factor Xa complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Protein C inhibitor-coagulation factor XI complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Protein C inhibitor-coagulation factor XI complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Abnormality of coagulation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of coagulation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Coagulation factor deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Coagulation factor deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
End-stage coagulation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the End-stage coagulation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Coagulation factor levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coagulation factor levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
COAGULATION FACTOR IX Gene Set From DGIdb Drug Targets 2026 interacting proteins for the COAGULATION FACTOR IX drug from theDGIdb Drug Targets 2026 dataset.
COAGULATION FACTOR VIIA Gene Set From DGIdb Drug Targets 2026 interacting proteins for the COAGULATION FACTOR VIIA drug from theDGIdb Drug Targets 2026 dataset.
COAGULATION FACTOR X HUMAN Gene Set From DGIdb Drug Targets 2026 interacting proteins for the COAGULATION FACTOR X HUMAN drug from theDGIdb Drug Targets 2026 dataset.
COAGULATION FACTOR X, HUMAN Gene Set From DGIdb Drug Targets 2026 interacting proteins for the COAGULATION FACTOR X, HUMAN drug from theDGIdb Drug Targets 2026 dataset.
COAGULATION FACTOR VII HUMAN Gene Set From DGIdb Drug Targets 2026 interacting proteins for the COAGULATION FACTOR VII HUMAN drug from theDGIdb Drug Targets 2026 dataset.
COAGULATION FACTOR VIIA (RECOMBINANT)-JNCW Gene Set From DGIdb Drug Targets 2026 interacting proteins for the COAGULATION FACTOR VIIA (RECOMBINANT)-JNCW drug from theDGIdb Drug Targets 2026 dataset.
COAGULATION FACTOR IX (RECOMBINANT), GLYCOPEGYLATED Gene Set From DGIdb Drug Targets 2026 interacting proteins for the COAGULATION FACTOR IX (RECOMBINANT), GLYCOPEGYLATED drug from theDGIdb Drug Targets 2026 dataset.
COAGULATION FACTOR IX HUMAN Gene Set From DGIdb Drug Targets 2026 interacting proteins for the COAGULATION FACTOR IX HUMAN drug from theDGIdb Drug Targets 2026 dataset.
COAGULATION FACTOR IX RECOMBINANT HUMAN Gene Set From DGIdb Drug Targets 2026 interacting proteins for the COAGULATION FACTOR IX RECOMBINANT HUMAN drug from theDGIdb Drug Targets 2026 dataset.
lectin induced complement pathway Gene Set From Biocarta Pathways proteins participating in the lectin induced complement pathway pathway from the Biocarta Pathways dataset.
classical complement pathway Gene Set From Biocarta Pathways proteins participating in the classical complement pathway pathway from the Biocarta Pathways dataset.
alternative complement pathway Gene Set From Biocarta Pathways proteins participating in the alternative complement pathway pathway from the Biocarta Pathways dataset.
Complement component 7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement component 7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement factor d deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement factor d deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement component 8 deficiency type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement component 8 deficiency type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement component 9 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement component 9 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement component 6 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement component 6 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement 1s deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement 1s deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement factor B deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement factor B deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
complement component c1 complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the complement component c1 complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
complement component c1 complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the complement component c1 complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I from the curated CTD Gene-Disease Associations dataset.
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II from the curated CTD Gene-Disease Associations dataset.
COMPLEMENT COMPONENT C1r/C1s DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT C1r/C1s DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Complement component 5 deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement component 5 deficiency from the curated CTD Gene-Disease Associations dataset.
Complement Component 7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Component 7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Complement Component 4, Partial Deficiency Of Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Component 4, Partial Deficiency Of from the curated CTD Gene-Disease Associations dataset.
Complement Factor H Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Factor H Deficiency from the curated CTD Gene-Disease Associations dataset.
COMPLEMENT COMPONENT 2 DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT 2 DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Complement Factor I Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Factor I Deficiency from the curated CTD Gene-Disease Associations dataset.
Complement Component 6 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Component 6 Deficiency from the curated CTD Gene-Disease Associations dataset.
Complement C4b-Binding Protein Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Complement C4b-Binding Protein in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
complement deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease complement deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
complement factor i deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease complement factor i deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
complement deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease complement deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
complement factor i deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease complement factor i deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
complement component 5 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease complement component 5 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
complement c4 complotypes Gene Set From GAD Gene-Disease Associations genes associated with the disease complement c4 complotypes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complement c4b-binding protein Gene Set From GAD Gene-Disease Associations genes associated with the disease complement c4b-binding protein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complement Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term complement in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
complement component c5a signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the complement component c5a signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of complement activation, lectin pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of complement activation, lectin pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
complement activation, classical pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of complement activation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of complement activation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of complement activation, alternative pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of complement activation, alternative pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of complement activation, alternative pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of complement activation, alternative pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
complement activation Gene Set From GO Biological Process Annotations 2015 genes participating in the complement activation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of complement activation, lectin pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of complement activation, lectin pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of complement activation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of complement activation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of complement activation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of complement activation biological process from the curated GO Biological Process Annotations 2015 dataset.
complement activation, lectin pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the complement activation, lectin pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of complement-dependent cytotoxicity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of complement-dependent cytotoxicity biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of complement activation, classical pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of complement activation, classical pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
complement activation, alternative pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the complement activation, alternative pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of complement-dependent cytotoxicity Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of complement-dependent cytotoxicity biological process from the curated GO Biological Process Annotations 2015 dataset.
complement-dependent cytotoxicity Gene Set From GO Biological Process Annotations 2015 genes participating in the complement-dependent cytotoxicity biological process from the curated GO Biological Process Annotations 2015 dataset.
complement receptor mediated signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the complement receptor mediated signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
complement component c1 complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the complement component c1 complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
complement binding Gene Set From GO Molecular Function Annotations 2015 genes performing the complement binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
complement component c3a receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the complement component c3a receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
complement component c1q binding Gene Set From GO Molecular Function Annotations 2015 genes performing the complement component c1q binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
complement component c4b binding Gene Set From GO Molecular Function Annotations 2015 genes performing the complement component c4b binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
complement component c3b receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the complement component c3b receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
complement receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the complement receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
complement component c5a binding Gene Set From GO Molecular Function Annotations 2015 genes performing the complement component c5a binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
complement component c4b receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the complement component c4b receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
complement component c5a receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the complement component c5a receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
complement component c3b binding Gene Set From GO Molecular Function Annotations 2015 genes performing the complement component c3b binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
complement deficiency Gene Set From GWASdb SNP-Disease Associations genes associated with the disease complement deficiency in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of complement system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of complement system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of complement system Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of complement system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
depletion of components of the alternative complement pathway Gene Set From HPO Gene-Disease Associations genes associated with the depletion of components of the alternative complement pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complement deficiency Gene Set From HPO Gene-Disease Associations genes associated with the complement deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement c9 Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement c9 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement c3 Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement c3 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement factor b Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement factor b phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement factor h Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement factor h phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement factor i Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement factor i phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dysfunctional alternative complement pathway Gene Set From HPO Gene-Disease Associations genes associated with the dysfunctional alternative complement pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the alternate complement pathway Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the alternate complement pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Peptidase S1A, complement C1r/C1S/mannan-binding Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase S1A, complement C1r/C1S/mannan-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Anaphylatoxin, complement system domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Anaphylatoxin, complement system domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Complement factor B Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Complement factor B protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Complement Clr-like EGF domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Complement Clr-like EGF domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Alpha-macroglobulin complement component Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Alpha-macroglobulin complement component protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Anaphylatoxin, complement system Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Anaphylatoxin, complement system protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Complement B/C2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Complement B/C2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Membrane attack complex component/perforin/complement C9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane attack complex component/perforin/complement C9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Complement C1q protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Complement C1q protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
decreased circulating complement protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating complement protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal circulating complement protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating complement protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
impaired lectin complement pathway Gene Set From MPO Gene-Phenotype Associations gene mutations causing the impaired lectin complement pathway phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
impaired complement classical pathway Gene Set From MPO Gene-Phenotype Associations gene mutations causing the impaired complement classical pathway phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
impaired complement alternative pathway Gene Set From MPO Gene-Phenotype Associations gene mutations causing the impaired complement alternative pathway phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal complement pathway Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal complement pathway phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal complement protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal complement protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complement factor d deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the complement factor d deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
complement component 4, partial deficiency of Gene Set From OMIM Gene-Disease Associations genes associated with the complement component 4, partial deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.
complement factor h deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the complement factor h deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
?complement factor b deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ?complement factor b deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
complement factor i deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the complement factor i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
Alternative complement activation Gene Set From Reactome Pathways 2014 proteins participating in the Alternative complement activation pathway from the Reactome Pathways dataset.
Complement cascade Gene Set From Reactome Pathways 2014 proteins participating in the Complement cascade pathway from the Reactome Pathways dataset.
Regulation of Complement cascade Gene Set From Reactome Pathways 2014 proteins participating in the Regulation of Complement cascade pathway from the Reactome Pathways dataset.
Initial triggering of complement Gene Set From Reactome Pathways 2014 proteins participating in the Initial triggering of complement pathway from the Reactome Pathways dataset.
Lectin pathway of complement activation Gene Set From Reactome Pathways 2014 proteins participating in the Lectin pathway of complement activation pathway from the Reactome Pathways dataset.
Terminal pathway of complement Gene Set From Reactome Pathways 2014 proteins participating in the Terminal pathway of complement pathway from the Reactome Pathways dataset.
Classical antibody-mediated complement activation Gene Set From Reactome Pathways 2014 proteins participating in the Classical antibody-mediated complement activation pathway from the Reactome Pathways dataset.
Complement Activation, Classical Pathway(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Complement Activation, Classical Pathway(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Complement Component 2 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complement Component 2 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complement Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complement Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complement Component 8 Deficiency, Type Ii Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complement Component 8 Deficiency, Type Ii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complement Component 3 Deficiency, Autosomal Recessive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complement Component 3 Deficiency, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Decreased Serum Complement C4B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Decreased Serum Complement C4B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complement Component 8 Deficiency, Type I Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complement Component 8 Deficiency, Type I in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complement Factor B Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complement Factor B Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complement Component 4, Partial Deficiency Of, Due To Dysfunctional C1 Inhibitor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complement Component 4, Partial Deficiency Of, Due To Dysfunctional C1 Inhibitor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
C4 Complement Assay (Procedure) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype C4 Complement Assay (Procedure) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Serum Complement C3 Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Serum Complement C3 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Serum Complement C4 Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Serum Complement C4 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Serum Complement Factor I Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Serum Complement Factor I in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Complement System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Complement System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Complement Deficiency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complement Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Serum Complement C9 Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Serum Complement C9 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Serum Complement Factor B Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Serum Complement Factor B in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Serum Complement Factor H Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Serum Complement Factor H in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Depletion Of Components Of The Alternative Complement Pathway Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Depletion Of Components Of The Alternative Complement Pathway in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dysfunctional Alternative Complement Pathway Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysfunctional Alternative Complement Pathway in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
complement activation, lectin pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the complement activation, lectin pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
complement activation, classical pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
complement activation, alternative pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the complement activation, alternative pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of complement activation, lectin pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of complement activation, lectin pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
complement-mediated synapse pruning Gene Set From GO Biological Process Annotations 2023 genes participating in the complement-mediated synapse pruning biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of complement activation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of complement activation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of complement activation, classical pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of complement-dependent cytotoxicity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of complement-dependent cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of complement activation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of complement activation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of complement-dependent cytotoxicity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of complement-dependent cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of complement activation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of complement activation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of complement activation, alternative pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of complement activation, alternative pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
complement receptor mediated signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the complement receptor mediated signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of complement activation, alternative pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of complement activation, alternative pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
complement component C5a signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the complement component C5a signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of complement activation, classical pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of complement activation, lectin pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of complement activation, lectin pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of complement activation, classical pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
complement component C4b binding Gene Set From GO Molecular Function Annotations 2023 genes performing the complement component C4b binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
complement component C3b binding Gene Set From GO Molecular Function Annotations 2023 genes performing the complement component C3b binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
complement component C4b receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the complement component C4b receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
complement component C3b receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the complement component C3b receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
complement receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the complement receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
complement component C5a receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the complement component C5a receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
complement component C3a binding Gene Set From GO Molecular Function Annotations 2023 genes performing the complement component C3a binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
complement component C3a receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the complement component C3a receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
abnormal complement pathway Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal complement pathway phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired complement alternative pathway Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired complement alternative pathway phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased circulating complement protein level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating complement protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal complement protein level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal complement protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired complement classical pathway Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired complement classical pathway phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal circulating complement protein level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating complement protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired lectin complement pathway Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired lectin complement pathway phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased serum complement activity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased serum complement activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased complement C5 level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased complement C5 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased circulating complement protein level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating complement protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Complement-secreting cancer associated fibroblast_Pancreas_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Complement-secreting cancer associated fibroblast_Pancreas_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Complement system Gene Set From WikiPathways Pathways 2024 proteins participating in the Complement system pathway from the WikiPathways Pathways 2024 dataset.
Fibrin complement receptor 3 signaling Gene Set From WikiPathways Pathways 2024 proteins participating in the Fibrin complement receptor 3 signaling pathway from the WikiPathways Pathways 2024 dataset.
Complement mediated inflammation of pulmonary alveolus in COVID 19 hypothetical pathway Gene Set From WikiPathways Pathways 2024 proteins participating in the Complement mediated inflammation of pulmonary alveolus in COVID 19 hypothetical pathway pathway from the WikiPathways Pathways 2024 dataset.
Complement activation Gene Set From WikiPathways Pathways 2024 proteins participating in the Complement activation pathway from the WikiPathways Pathways 2024 dataset.
Alternative complement activation Gene Set From Reactome Pathways 2024 proteins participating in the Alternative complement activation pathway from the Reactome Pathways 2024 dataset.
Classical antibody-mediated complement activation Gene Set From Reactome Pathways 2024 proteins participating in the Classical antibody-mediated complement activation pathway from the Reactome Pathways 2024 dataset.
Complement cascade Gene Set From Reactome Pathways 2024 proteins participating in the Complement cascade pathway from the Reactome Pathways 2024 dataset.
Initial triggering of complement Gene Set From Reactome Pathways 2024 proteins participating in the Initial triggering of complement pathway from the Reactome Pathways 2024 dataset.
Lectin pathway of complement activation Gene Set From Reactome Pathways 2024 proteins participating in the Lectin pathway of complement activation pathway from the Reactome Pathways 2024 dataset.
Regulation of Complement cascade Gene Set From Reactome Pathways 2024 proteins participating in the Regulation of Complement cascade pathway from the Reactome Pathways 2024 dataset.
Terminal pathway of complement Gene Set From Reactome Pathways 2024 proteins participating in the Terminal pathway of complement pathway from the Reactome Pathways 2024 dataset.
complement activation, lectin pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the complement activation, lectin pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
complement activation, classical pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
complement activation, alternative pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the complement activation, alternative pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of complement activation, lectin pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of complement activation, lectin pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
complement-mediated synapse pruning Gene Set From GO Biological Process Annotations 2025 genes participating in the complement-mediated synapse pruning biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of complement activation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of complement activation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of complement activation, classical pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of complement-dependent cytotoxicity Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of complement-dependent cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of complement activation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of complement activation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of complement-dependent cytotoxicity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of complement-dependent cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of complement activation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of complement activation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of complement activation, alternative pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of complement activation, alternative pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
complement receptor mediated signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the complement receptor mediated signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of complement activation, alternative pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of complement activation, alternative pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
complement component C5a signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the complement component C5a signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of complement activation, classical pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of complement activation, lectin pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of complement activation, lectin pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of complement activation, classical pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of complement activation, classical pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
complement component C4b binding Gene Set From GO Molecular Function Annotations 2025 genes performing the complement component C4b binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
complement component C3b binding Gene Set From GO Molecular Function Annotations 2025 genes performing the complement component C3b binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
complement component C4b receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the complement component C4b receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
complement component C3b receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the complement component C3b receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
complement receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the complement receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
complement component C5a receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the complement component C5a receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
complement component C3a binding Gene Set From GO Molecular Function Annotations 2025 genes performing the complement component C3a binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
complement component C3a receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the complement component C3a receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Complement deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Complement deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Complement factor I deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Complement factor I deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Complement component 2 deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Complement component 2 deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Complement deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complement deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complement component 4a deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complement component 4a deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complement component 3 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complement component 3 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complement component 5 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complement component 5 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complement component 7 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complement component 7 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complement component 2 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complement component 2 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complement component 6 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complement component 6 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complement factor I deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complement factor I deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complement component 9 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complement component 9 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complement component C1 complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Complement component C1 complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Complement component C1q complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Complement component C1q complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Complement component C1q complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Complement component C1q complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Complement component C1 complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Complement component C1 complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
classical-complement-pathway C3/C5 convertase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the classical-complement-pathway C3/C5 convertase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Complement component 7 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Complement component 7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Complement component 2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Complement component 2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Complement factor b deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Complement factor b deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Complement component 8 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Complement component 8 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Complement component 6 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Complement component 6 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
COMPLEMENT COMPONENT Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the COMPLEMENT COMPONENT phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Complement component 9 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Complement component 9 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Complement component 5 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Complement component 5 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Complement component 3 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Complement component 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Complement component C1s deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Complement component C1s deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immunodeficiency due to a late component of complement deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to a late component of complement deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Complement factor H binding to malondialdehyde Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complement factor H binding to malondialdehyde phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Serum C3d:C3 ratio (systemic complement activation) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum C3d:C3 ratio (systemic complement activation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Complement C3 levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complement C3 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Complement C4 levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complement C4 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Complement factor H levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complement factor H levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Complement factor H-related protein 1 levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complement factor H-related protein 1 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Complement factor H-related protein 2 levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complement factor H-related protein 2 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Complement factor H-related protein 3 levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complement factor H-related protein 3 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Complement factor H-related protein 4A levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complement factor H-related protein 4A levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Complement factor H-related protein 5 levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complement factor H-related protein 5 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety and hostility and depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamins and metabolites in pregnant women and neonates Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2014 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2014 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2014 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2014 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2014 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.
SRF and miRs in smooth muscle differentiation and proliferation Gene Set From WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene Set From WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene Set From WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.
Somatroph axis GH and its relationship to dietary restriction and aging Gene Set From WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset.
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene Set From WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2024 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset.
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2024 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset.
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Set From Reactome Pathways 2024 proteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2024 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2024 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset.
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Set From Reactome Pathways 2024 proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset.
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2024 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Regulation of gene expression and signal transduction in immune and stress responses Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Basic cell groups and regions Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
head and face region of M1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
telomeres telomerase cellular aging and immortality Gene Set From Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.
mcalpain and friends in cell motility Gene Set From Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.
role of ppar-gamma coactivators in obesity and thermogenesis Gene Set From Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.
il12 and stat4 dependent signaling pathway in th1 development Gene Set From Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.
hypoxia and p53 in the cardiovascular system Gene Set From Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.
lissencephaly gene (lis1) in neuronal migration and development Gene Set From Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.
role of erbb2 in signal transduction and oncology Gene Set From Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.
corticosteroids and cardioprotection Gene Set From Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.
cyclins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.
mechanism of acetaminophen activity and toxicity Gene Set From Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.
nfat and hypertrophy of the heart Gene Set From Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.
acetylation and deacetylation of rela in nucleus Gene Set From Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.
thrombin signaling and protease-activated receptors Gene Set From Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.
antigen processing and presentation Gene Set From Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.
stathmin and breast cancer resistance to antimicrotubule agents Gene Set From Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.
role of ß-arrestins in the activation and targeting of map kinases Gene Set From Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set From Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set From Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.
btg family proteins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set From Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.
endocytotic role of ndk phosphins and dynamin Gene Set From Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.
regulation of eif-4e and p70s6 kinase Gene Set From Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set From Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.
vegf hypoxia and angiogenesis Gene Set From Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.
yaci and bcma stimulation of b cell immune responses Gene Set From Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.
lck and fyn tyrosine kinases in initiation of tcr activation Gene Set From Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.
hiv-1 nef: negative effector of fas and tnf Gene Set From Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set From Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.
ucalpain and friends in cell spread Gene Set From Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.
ionomycin and phorbal ester signaling pathway Gene Set From Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.
carm1 and regulation of the estrogen receptor Gene Set From Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.
phosphoinositides and their downstream targets Gene Set From Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.
melanocyte development and pigmentation pathway Gene Set From Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.
akap95 role in mitosis and chromosome dynamics Gene Set From Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.
transcription factor creb and its extracellular signals Gene Set From Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.
visceral fat deposits and the metabolic syndrome Gene Set From Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.
the igf-1 receptor and longevity Gene Set From Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.
cdc25 and chk1 regulatory pathway in response to dna damage Gene Set From Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.
human cytomegalovirus and map kinase pathways Gene Set From Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.
influence of ras and rho proteins on g1 to s transition Gene Set From Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.
proteolysis and signaling pathway of notch Gene Set From Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.
apoptotic dna-fragmentation and tissue homeostasis Gene Set From Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.
ion channels and their functional role in vascular endothelium Gene Set From Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set From Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.
fosb gene expression and drug abuse Gene Set From Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.
links between pyk2 and map kinases Gene Set From Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.
opposing roles of aif in apoptosis and cell survival Gene Set From Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.
degradation of the rar and rxr by the proteasome Gene Set From Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.
cadmium induces dna synthesis and proliferation in macrophages Gene Set From Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set From Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.
role of brca1 brca2 and atr in cancer susceptibility Gene Set From Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.
chrebp regulation by carbohydrates and camp Gene Set From Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.
pten dependent cell cycle arrest and apoptosis Gene Set From Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.
induction of apoptosis through dr3 and dr4/5 death receptors Gene Set From Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.
CIITA-18437201-Raji B cells and iDC-human Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
VDR-23401126-LCL-AND-THP1-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Hypothyroidism, central, and testicular enlargement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, mental retardation, and seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vater association with macrocephaly and ventriculomegaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microtia, hearing impairment, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, spastic quadriplegia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined cellular and humoral immune defects with granulomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation with language impairment and autistic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, anterior maxillary protrusion, and strabismus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple Cutaneous and Mucosal Venous Malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy hereditary sensory and autonomic type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly with mental retardation and digital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia sideroblastic and spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mullerian aplasia and hyperandrogenism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Knuckle pads, deafness AND leukonychia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multicentric osteolysis, nodulosis and arthropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stapes ankylosis with broad thumb and toes Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, short stature, and impaired glucose metabolism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy dilated with woolly hair and keratoderma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract and cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, microphthalmia and nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and anterior segment dysgenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone fragility with contractures, arterial rupture, and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ulna and fibula absence of with severe limb deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor v and factor viii, combined deficiency of, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary Paragangliomas and Pheochromocytomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Band-like calcification with simplified gyration and polymicrogyria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, epilepsy, and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, juvenile, with microcornea and glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, deafness, and narcolepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary motor and sensory neuropathy with optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary leiomyomatosis and renal cell cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Monocyte and dendritic cell deficiency, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, hiatal hernia and nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pancreatic agenesis and congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined malonic and methylmalonic aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis Gyrata syndrome of Beare and Stevenson Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aniridia, cerebellar ataxia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked hereditary motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniosynostosis and dental anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Obesity, hyperphagia, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebroretinal microangiopathy with calcifications and cysts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy and paroxysmal dyskinesia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alacrima, achalasia, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, normal intelligence and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Calcification of joints and arteries Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypotrichosis and recurrent skin vesicles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutaneous telangiectasia and cancer syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pineal hyperplasia AND diabetes mellitus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Morbid obesity and spermatogenic failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skeletal defects, genital hypoplasia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary sensory and autonomic neuropathy type IIA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia, high, with cataract and vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined deficiency of factor V and factor VIII, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Camptodactyly, tall stature, and hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyogenic arthritis, pyoderma gangrenosum and acne Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth deficiency and mental retardation with facial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, cochlear, with myopia and intellectual impairment Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined deficiency of sialidase AND beta galactosidase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mitochondrial sorting and assembly machinery complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
collagen and cuticulin-based cuticle extracellular matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
collagen and cuticulin-based cuticle extracellular matrix part Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mitochondrial sorting and assembly machinery complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Set From CORUM Protein Complexes proteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset.
NRD complex (Nucleosome remodeling and deacetylation complex) Gene Set From CORUM Protein Complexes proteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset.
6S methyltransferase and RG-containing Sm proteins complex Gene Set From CORUM Protein Complexes proteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset.
Remodeling and spacing factor (RSF) complex Gene Set From CORUM Protein Complexes proteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset.
PBAF complex (Polybromo- and BAF containing complex) Gene Set From CORUM Protein Complexes proteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset.
Cleavage and polyadenylation factor (CPSF) Gene Set From CORUM Protein Complexes proteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset.
Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Nucleic and chromatin Fanconi complex Gene Set From CORUM Protein Complexes proteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset.
Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset.
ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Set From CORUM Protein Complexes proteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.
20S methylosome and RG-containing Sm protein complex Gene Set From CORUM Protein Complexes proteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset.
Amino Acids, Peptides, and Proteins Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset.
Bile Acids and Salts Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset.
Prime and Bond NT Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset.
drospirenone and ethinyl estradiol combination Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset.
Hypophosphatemic Rickets And Hyperparathyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset.
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.
Synovitis granulomatous with uveitis and cranial neuropathies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.
Hereditary Sensory and Motor Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.
Preaxial deficiency, postaxial polydactyly and hypospadias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset.
Combined Cellular And Humoral Immune Defects With Granulomas Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.
OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset.
Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset.
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset.
Microtia, Hearing Impairment, And Cleft Palate Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset.
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset.
Acromegaloid features, overgrowth, cleft palate, and hernia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.
46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset.
Craniosynostosis, anal anomalies, and porokeratosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset.
Sacral defect and anterior sacral meningocele Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.
Classical Lissencephalies and Subcortical Band Heterotopias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Classical Lissencephalies and Subcortical Band Heterotopias from the curated CTD Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 1 and deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, Russe type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset.
Blepharophimosis, Ptosis, and Epicanthus Inversus Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Blepharophimosis, Ptosis, and Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset.
Hypotrichosis And Recurrent Skin Vesicles Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.
Signs and Symptoms, Digestive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Signs and Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.
Methylmalonic Aciduria and Homocystinuria, CblD Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblD Type from the curated CTD Gene-Disease Associations dataset.
Head and Neck Neoplasms Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Head and Neck Neoplasms from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.
Cataract, Juvenile, With Microcornea And Glucosuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset.
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset.
Venous Malformations, Multiple Cutaneous and Mucosal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset.
BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset.
Postoperative Nausea and Vomiting Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Postoperative Nausea and Vomiting from the curated CTD Gene-Disease Associations dataset.
Myopathy with lactic acidosis and sideroblastic anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.
Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.
Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.
Hypopituitarism and septooptic 'dysplasia' Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset.
PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset.
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset.
Aplasia of Lacrimal and Salivary Glands Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset.
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset.
Calcification of Joints and Arteries Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Calcification of Joints and Arteries from the curated CTD Gene-Disease Associations dataset.
CHOANAL ATRESIA AND LYMPHEDEMA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHOANAL ATRESIA AND LYMPHEDEMA from the curated CTD Gene-Disease Associations dataset.
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis from the curated CTD Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy, Type IIC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset.
Asthma, Nasal Polyps, And Aspirin Intolerance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Asthma, Nasal Polyps, And Aspirin Intolerance from the curated CTD Gene-Disease Associations dataset.
Neoplasms, Germ Cell and Embryonal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Germ Cell and Embryonal from the curated CTD Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy VI Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset.
Cutis Gyrata Syndrome of Beare And Stevenson Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Gyrata Syndrome of Beare And Stevenson from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.
Wounds and Injuries Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wounds and Injuries from the curated CTD Gene-Disease Associations dataset.
Schizophrenia and Disorders with Psychotic Features Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Schizophrenia and Disorders with Psychotic Features from the curated CTD Gene-Disease Associations dataset.
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset.
Sleep Initiation and Maintenance Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Initiation and Maintenance Disorders from the curated CTD Gene-Disease Associations dataset.
Methylmalonic Aciduria and Homocystinuria, CblF Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblF Type from the curated CTD Gene-Disease Associations dataset.
Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Cataract and cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Harmonizome 3.0

Complement and Coagulation Cascades(Mus musculus) Gene Set

complement and coagulation cascades Gene Set

Complement and Coagulation Cascades(Homo sapiens) Gene Set

Dengue 2 interactions with complement and coagulation cascades Gene Set

Complement and coagulation cascades Gene Set

Complement and coagulation cascades Gene Set

Complement Activation, Classical Pathway(Mus musculus) Gene Set

SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set

Glycolysis and Gluconeogenesis(Mus musculus) Gene Set

Glutathione and one carbon metabolism(Mus musculus) Gene Set

One carbon metabolism and related pathways(Mus musculus) Gene Set

Serotonin and anxiety(Mus musculus) Gene Set

Synthesis and Degradation of Ketone Bodies(Mus musculus) Gene Set

Prostaglandin Synthesis and Regulation(Mus musculus) Gene Set

Cytokines and Inflammatory Response (BioCarta)(Mus musculus) Gene Set

Alanine and aspartate metabolism(Mus musculus) Gene Set

Serotonin and anxiety-related events(Mus musculus) Gene Set

Leptin and adiponectin(Mus musculus) Gene Set

FAS pathway and Stress induction of HSP regulation(Mus musculus) Gene Set

Myometrial Relaxation and Contraction Pathways(Mus musculus) Gene Set

Wnt Signaling Pathway and Pluripotency(Mus musculus) Gene Set

Nuclear receptors in lipid metabolism and toxicity(Mus musculus) Gene Set

Mus musculus Gene Set

Regulation of Cardiac Hypertrophy by miR-208(Mus musculus) Gene Set

Chemokine signaling pathway(Mus musculus) Gene Set

Hypertrophy Model(Mus musculus) Gene Set

Peptide GPCRs(Mus musculus) Gene Set

Apoptosis(Mus musculus) Gene Set

GPCRs, Class B Secretin-like(Mus musculus) Gene Set

SIDS Susceptibility Pathways(Mus musculus) Gene Set

miR-1 in cardiac development(Mus musculus) Gene Set

Biogenic Amine Synthesis(Mus musculus) Gene Set

G13 Signaling Pathway(Mus musculus) Gene Set

ESC Pluripotency Pathways(Mus musculus) Gene Set

Triacylglyceride Synthesis(Mus musculus) Gene Set

Histone modifications(Mus musculus) Gene Set

Mismatch repair(Mus musculus) Gene Set

Ptf1a related regulatory pathway(Mus musculus) Gene Set

Id Signaling Pathway(Mus musculus) Gene Set

Cytoplasmic Ribosomal Proteins(Mus musculus) Gene Set

IL-6 signaling Pathway(Mus musculus) Gene Set

G1 to S cell cycle control(Mus musculus) Gene Set

Pentose Phosphate Pathway(Mus musculus) Gene Set

Signaling of Hepatocyte Growth Factor Receptor(Mus musculus) Gene Set

Folic Acid Network(Mus musculus) Gene Set

Methylation(Mus musculus) Gene Set

Non-odorant GPCRs(Mus musculus) Gene Set

Amino acid conjugation of benzoic acid(Mus musculus) Gene Set

EBV LMP1 signaling(Mus musculus) Gene Set

Hedgehog Signaling Pathway(Mus musculus) Gene Set

Proteasome Degradation(Mus musculus) Gene Set

MAPK signaling pathway(Mus musculus) Gene Set

Spinal Cord Injury(Mus musculus) Gene Set

Heart Development(Mus musculus) Gene Set

Selenium metabolism/Selenoproteins(Mus musculus) Gene Set

Leptin Insulin Overlap(Mus musculus) Gene Set

IL-7 Signaling Pathway(Mus musculus) Gene Set

EPO Receptor Signaling(Mus musculus) Gene Set

Glycogen Metabolism(Mus musculus) Gene Set

Mitochondrial Gene Expression(Mus musculus) Gene Set

Adipogenesis genes(Mus musculus) Gene Set

Fatty Acid Omega Oxidation(Mus musculus) Gene Set

Oxidative Stress(Mus musculus) Gene Set

Polyol pathway(Mus musculus) Gene Set

Mitochondrial LC-Fatty Acid Beta-Oxidation(Mus musculus) Gene Set

Ovarian Infertility Genes(Mus musculus) Gene Set

Calcium Regulation in the Cardiac Cell(Mus musculus) Gene Set

ACE Inhibitor Pathway(Mus musculus) Gene Set

Small Ligand GPCRs(Mus musculus) Gene Set

miRNA regulation of DNA Damage Response(Mus musculus) Gene Set

Kit Receptor Signaling Pathway(Mus musculus) Gene Set

Acetylcholine Synthesis(Mus musculus) Gene Set

Endochondral Ossification(Mus musculus) Gene Set

Glucocorticoid & Mineralcorticoid Metabolism(Mus musculus) Gene Set

PPAR signaling pathway(Mus musculus) Gene Set

Estrogen signalling(Mus musculus) Gene Set

Cholesterol Biosynthesis(Mus musculus) Gene Set

mRNA processing(Mus musculus) Gene Set

Diurnally Regulated Genes with Circadian Orthologs(Mus musculus) Gene Set