Vitamin A1 and A5 X pathways

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Results for "Vitamin A1 and A5 X pathways": 1001 gene sets

Name
Vitamin A1 and A5 X pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin A1 and A5 X pathways pathway from the WikiPathways Pathways 2024 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.
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.
Myometrial Relaxation and Contraction Pathways(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Myometrial Relaxation and Contraction Pathways(Homo sapiens) 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.
Trans sulfuration one carbon metabolism and related pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Trans sulfuration one carbon metabolism and related pathways pathway from the WikiPathways Pathways 2024 dataset.
Myometrial relaxation and contraction pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Myometrial relaxation and contraction pathways pathway from the WikiPathways Pathways 2024 dataset.
Amplification and expansion of oncogenic pathways as metastatic traits Gene Set From WikiPathways Pathways 2024 proteins participating in the Amplification and expansion of oncogenic pathways as metastatic traits pathway from the WikiPathways Pathways 2024 dataset.
Physico chemical features and toxicity associated pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Physico chemical features and toxicity associated pathways pathway from the WikiPathways Pathways 2024 dataset.
Factors and pathways affecting insulin like growth factor IGF1 Akt signaling Gene Set From WikiPathways Pathways 2024 proteins participating in the Factors and pathways affecting insulin like growth factor IGF1 Akt signaling pathway from the WikiPathways Pathways 2024 dataset.
Urea cycle and associated pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Urea cycle and associated pathways pathway from the WikiPathways Pathways 2024 dataset.
Pathways of nucleic acid metabolism and innate immune sensing Gene Set From WikiPathways Pathways 2024 proteins participating in the Pathways of nucleic acid metabolism and innate immune sensing pathway from the WikiPathways Pathways 2024 dataset.
Cholesterol metabolism with Bloch and Kandutsch Russell pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Cholesterol metabolism with Bloch and Kandutsch Russell pathways pathway from the WikiPathways Pathways 2024 dataset.
RAS and bradykinin pathways in COVID 19 Gene Set From WikiPathways Pathways 2024 proteins participating in the RAS and bradykinin pathways in COVID 19 pathway from the WikiPathways Pathways 2024 dataset.
Proline and hydroxyproline pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Proline and hydroxyproline pathways pathway from the WikiPathways Pathways 2024 dataset.
7 oxo C and 7 beta HC pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the 7 oxo C and 7 beta HC pathways pathway from the WikiPathways Pathways 2024 dataset.
Relevant molecular pathways and targeted agents in triple negative breast cancer Gene Set From WikiPathways Pathways 2024 proteins participating in the Relevant molecular pathways and targeted agents in triple negative breast cancer pathway from the WikiPathways Pathways 2024 dataset.
ADHD and autism ASD pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the ADHD and autism ASD pathways pathway from the WikiPathways Pathways 2024 dataset.
SARS-CoV-1 targets host intracellular signalling and regulatory pathways Gene Set From Reactome Pathways 2024 proteins participating in the SARS-CoV-1 targets host intracellular signalling and regulatory pathways pathway from the Reactome Pathways 2024 dataset.
SARS-CoV-2 targets host intracellular signalling and regulatory pathways Gene Set From Reactome Pathways 2024 proteins participating in the SARS-CoV-2 targets host intracellular signalling and regulatory pathways pathway from the Reactome Pathways 2024 dataset.
abnormal vitamin or vitamin cofactor metabolism Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin or vitamin cofactor metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Vitamin D levels (dietary vitamin D intake interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vitamin D levels (dietary vitamin D intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
regulation of map kinase pathways through dual specificity phosphatases Gene Set From Biocarta Pathways proteins participating in the regulation of map kinase pathways through dual specificity phosphatases pathway from the Biocarta Pathways dataset.
multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation Gene Set From Biocarta Pathways proteins participating in the multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation pathway from the Biocarta Pathways dataset.
pathways Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term pathways in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
ventricular preexcitation with multiple accessory pathways Gene Set From HPO Gene-Disease Associations genes associated with the ventricular preexcitation with multiple accessory pathways phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways Gene Set From Reactome Pathways 2014 proteins participating in the Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways pathway from the Reactome Pathways dataset.
NS1 Mediated Effects on Host Pathways Gene Set From Reactome Pathways 2014 proteins participating in the NS1 Mediated Effects on Host Pathways pathway from the Reactome Pathways dataset.
Regulatory RNA pathways Gene Set From Reactome Pathways 2014 proteins participating in the Regulatory RNA pathways pathway from the Reactome Pathways dataset.
RIG-I/MDA5 mediated induction of IFN-alpha/beta pathways Gene Set From Reactome Pathways 2014 proteins participating in the RIG-I/MDA5 mediated induction of IFN-alpha/beta pathways pathway from the Reactome Pathways dataset.
SIDS Susceptibility Pathways(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SIDS Susceptibility Pathways(Homo sapiens) 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.
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.
G Protein Signaling Pathways(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the G Protein Signaling Pathways(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Interferon type I signaling pathways(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Interferon type I signaling pathways(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Signaling Pathways in Glioblastoma(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Signaling Pathways in Glioblastoma(Homo sapiens) 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.
Methylation Pathways(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Methylation Pathways(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Endothelin Pathways(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Endothelin Pathways(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Ventricular Preexcitation With Multiple Accessory Pathways Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventricular Preexcitation With Multiple Accessory Pathways in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Endothelin pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Endothelin pathways pathway from the WikiPathways Pathways 2024 dataset.
Common pathways underlying drug addiction Gene Set From WikiPathways Pathways 2024 proteins participating in the Common pathways underlying drug addiction pathway from the WikiPathways Pathways 2024 dataset.
NAD biosynthetic pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the NAD biosynthetic pathways pathway from the WikiPathways Pathways 2024 dataset.
Pathways affected in adenoid cystic carcinoma Gene Set From WikiPathways Pathways 2024 proteins participating in the Pathways affected in adenoid cystic carcinoma pathway from the WikiPathways Pathways 2024 dataset.
Hypothesized pathways in pathogenesis of cardiovascular disease Gene Set From WikiPathways Pathways 2024 proteins participating in the Hypothesized pathways in pathogenesis of cardiovascular disease pathway from the WikiPathways Pathways 2024 dataset.
Embryonic stem cell pluripotency pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Embryonic stem cell pluripotency pathways pathway from the WikiPathways Pathways 2024 dataset.
Clear cell renal cell carcinoma pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Clear cell renal cell carcinoma pathways pathway from the WikiPathways Pathways 2024 dataset.
Thiamine metabolic pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Thiamine metabolic pathways pathway from the WikiPathways Pathways 2024 dataset.
Autosomal recessive osteopetrosis pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Autosomal recessive osteopetrosis pathways pathway from the WikiPathways Pathways 2024 dataset.
Overlap between signal transduction pathways contributing to LMNA laminopathies Gene Set From WikiPathways Pathways 2024 proteins participating in the Overlap between signal transduction pathways contributing to LMNA laminopathies pathway from the WikiPathways Pathways 2024 dataset.
DNA repair pathways full network Gene Set From WikiPathways Pathways 2024 proteins participating in the DNA repair pathways full network pathway from the WikiPathways Pathways 2024 dataset.
Opioid receptor pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Opioid receptor pathways pathway from the WikiPathways Pathways 2024 dataset.
Metabolic pathways of fibroblasts Gene Set From WikiPathways Pathways 2024 proteins participating in the Metabolic pathways of fibroblasts pathway from the WikiPathways Pathways 2024 dataset.
Affected pathways in Duchenne muscular dystrophy Gene Set From WikiPathways Pathways 2024 proteins participating in the Affected pathways in Duchenne muscular dystrophy pathway from the WikiPathways Pathways 2024 dataset.
Cancer pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Cancer pathways pathway from the WikiPathways Pathways 2024 dataset.
GNAQ pathways in port wine stain Gene Set From WikiPathways Pathways 2024 proteins participating in the GNAQ pathways in port wine stain pathway from the WikiPathways Pathways 2024 dataset.
Effect of omega 3 PUFA on Huntington 39 s disease pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Effect of omega 3 PUFA on Huntington 39 s disease pathways pathway from the WikiPathways Pathways 2024 dataset.
Methylation pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Methylation pathways pathway from the WikiPathways Pathways 2024 dataset.
Sudden infant death syndrome SIDS susceptibility pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Sudden infant death syndrome SIDS susceptibility pathways pathway from the WikiPathways Pathways 2024 dataset.
Bacterial Infection Pathways Gene Set From Reactome Pathways 2024 proteins participating in the Bacterial Infection Pathways pathway from the Reactome Pathways 2024 dataset.
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models Gene Set From Reactome Pathways 2024 proteins participating in the Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models pathway from the Reactome Pathways 2024 dataset.
NS1 Mediated Effects on Host Pathways Gene Set From Reactome Pathways 2024 proteins participating in the NS1 Mediated Effects on Host Pathways pathway from the Reactome Pathways 2024 dataset.
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways Gene Set From Reactome Pathways 2024 proteins participating in the Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways pathway from the Reactome Pathways 2024 dataset.
Parasitic Infection Pathways Gene Set From Reactome Pathways 2024 proteins participating in the Parasitic Infection Pathways pathway from the Reactome Pathways 2024 dataset.
Viral Infection Pathways Gene Set From Reactome Pathways 2024 proteins participating in the Viral Infection Pathways pathway from the Reactome Pathways 2024 dataset.
Signaling pathways regulating pluripotency of stem cells Gene Set From KEGG Pathways 2026 proteins participating in the Signaling pathways regulating pluripotency of stem cells pathway from the KEGG Pathways 2026 dataset.
Pathways in cancer Gene Set From KEGG Pathways 2026 proteins participating in the Pathways in cancer pathway from the KEGG Pathways 2026 dataset.
Pathways of neurodegeneration - multiple diseases Gene Set From KEGG Pathways 2026 proteins participating in the Pathways of neurodegeneration - multiple diseases pathway from the KEGG Pathways 2026 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.
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
homocysteine, folate and vitamin b12 levels Gene Set From GAD Gene-Disease Associations genes associated with the disease homocysteine, folate and vitamin b12 levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
plasma folate vitamin b12 homocyst(e)ine and colorectal cancer risk Gene Set From GAD Gene-Disease Associations genes associated with the disease plasma folate vitamin b12 homocyst(e)ine and colorectal cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin e and carotenoids Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin e and carotenoids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
Vitamin D metabolism and pathway Gene Set From PANTHER Pathways proteins participating in the Vitamin D metabolism and pathway pathway from the PANTHER Pathways dataset.
Metabolism of steroid hormones and vitamin D Gene Set From Reactome Pathways 2014 proteins participating in the Metabolism of steroid hormones and vitamin D pathway from the Reactome Pathways dataset.
Defects in vitamin and cofactor metabolism Gene Set From Reactome Pathways 2014 proteins participating in the Defects in vitamin and cofactor metabolism pathway from the Reactome Pathways dataset.
Cobalamin (Cbl, vitamin B12) transport and metabolism Gene Set From Reactome Pathways 2014 proteins participating in the Cobalamin (Cbl, vitamin B12) transport and metabolism pathway from the Reactome Pathways dataset.
Vitamin A and Carotenoid Metabolism(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Vitamin A and Carotenoid Metabolism(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin B6 dependent and responsive disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin B6 dependent and responsive disorders pathway from the WikiPathways Pathways 2024 dataset.
Vitamin K metabolism and activation of dependent proteins Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin K metabolism and activation of dependent proteins pathway from the WikiPathways Pathways 2024 dataset.
Vitamin A and carotenoid metabolism Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin A and carotenoid metabolism pathway from the WikiPathways Pathways 2024 dataset.
Cobalamin (Cbl, vitamin B12) transport and metabolism Gene Set From Reactome Pathways 2024 proteins participating in the Cobalamin (Cbl, vitamin B12) transport and metabolism pathway from the Reactome Pathways 2024 dataset.
Defects in vitamin and cofactor metabolism Gene Set From Reactome Pathways 2024 proteins participating in the Defects in vitamin and cofactor metabolism pathway from the Reactome Pathways 2024 dataset.
Hereditary hypercarotenemia and vitamin A deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary hypercarotenemia and vitamin A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Vitamin digestion and absorption Gene Set From KEGG Pathways 2026 proteins participating in the Vitamin digestion and absorption pathway from the KEGG Pathways 2026 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.
control of gene expression by vitamin d receptor Gene Set From Biocarta Pathways proteins participating in the control of gene expression by vitamin d receptor pathway from the Biocarta Pathways dataset.
Vitamin d hydroxylation-deficient rickets, type 1b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitamin d hydroxylation-deficient rickets, type 1b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitamin D-dependent rickets, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitamin D-dependent rickets, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitamin D-dependent rickets, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitamin D-dependent rickets, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia with vitamin E deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia with vitamin E deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitamin k-dependent clotting factors, combined deficiency of, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitamin k-dependent clotting factors, combined deficiency of, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitamin k-dependent clotting factors, combined deficiency of, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitamin k-dependent clotting factors, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
vitamin K1 oxide Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical vitamin K1 oxide from the curated CTD Gene-Chemical Interactions dataset.
Vitamin K 3 Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Vitamin K 3 from the curated CTD Gene-Chemical Interactions dataset.
Vitamin K 1 Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Vitamin K 1 from the curated CTD Gene-Chemical Interactions dataset.
dihydroxy-vitamin D3 Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical dihydroxy-vitamin D3 from the curated CTD Gene-Chemical Interactions dataset.
Vitamin U Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Vitamin U from the curated CTD Gene-Chemical Interactions dataset.
Vitamin A Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Vitamin A from the curated CTD Gene-Chemical Interactions dataset.
Vitamin E Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Vitamin E from the curated CTD Gene-Chemical Interactions dataset.
Vitamin D Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Vitamin D from the curated CTD Gene-Chemical Interactions dataset.
Vitamin K Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Vitamin K from the curated CTD Gene-Chemical Interactions dataset.
1,25-dihydroxy-16-ene-vitamin D3 Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 1,25-dihydroxy-16-ene-vitamin D3 from the curated CTD Gene-Chemical Interactions dataset.
Vitamin K 2 Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Vitamin K 2 from the curated CTD Gene-Chemical Interactions dataset.
Vitamin B 6 Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Vitamin B 6 from the curated CTD Gene-Chemical Interactions dataset.
Vitamin B 12 Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Vitamin B 12 from the curated CTD Gene-Chemical Interactions dataset.
Vitamin B 12 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin B 12 Deficiency from the curated CTD Gene-Disease Associations dataset.
Vitamin A Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin A Deficiency from the curated CTD Gene-Disease Associations dataset.
Vitamin D Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin D Deficiency from the curated CTD Gene-Disease Associations dataset.
Ataxia with vitamin E deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia with vitamin E deficiency from the curated CTD Gene-Disease Associations dataset.
Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1 from the curated CTD Gene-Disease Associations dataset.
Vitamin D Hydroxylation-Deficient Rickets, Type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin D Hydroxylation-Deficient Rickets, Type 1A from the curated CTD Gene-Disease Associations dataset.
Vitamin D-Dependent Rickets, Type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin D-Dependent Rickets, Type 2A from the curated CTD Gene-Disease Associations dataset.
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset.
Vitamin E Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin E Deficiency from the curated CTD Gene-Disease Associations dataset.
Vitamin D Hydroxylation-Deficient Rickets, Type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin D Hydroxylation-Deficient Rickets, Type 1B from the curated CTD Gene-Disease Associations dataset.
VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1 from the curated CTD Gene-Disease Associations dataset.
Vitamin B 12 Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Vitamin B 12 in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Vitamin A Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Vitamin A in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Vitamin D Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Vitamin D in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Vitamin K Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Vitamin K in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Vitamin E Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Vitamin E in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Vitamin B 6 Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Vitamin B 6 in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
vitamin metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitamin metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vitamin b12 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitamin b12 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vitamin k deficiency hemorrhagic disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitamin k deficiency hemorrhagic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
Vitamin C Gene Set From DrugBank Drug Targets interacting proteins for the Vitamin C drug from the curated DrugBank Drug Targets dataset.
Vitamin E Gene Set From DrugBank Drug Targets interacting proteins for the Vitamin E drug from the curated DrugBank Drug Targets dataset.
Vitamin A Gene Set From DrugBank Drug Targets interacting proteins for the Vitamin A drug from the curated DrugBank Drug Targets dataset.
thromboembolism; venous thrombosis; vitamin b deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease thromboembolism; venous thrombosis; vitamin b deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
altered b vitamin/thiol metabolism Gene Set From GAD Gene-Disease Associations genes associated with the disease altered b vitamin/thiol metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin b 6 Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin b 6 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin b12 levels Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin b12 levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv; folate; vitamin b12 Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv; folate; vitamin b12 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin b 12 Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin b 12 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes, gestational; vitamin d deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, gestational; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
homocysteine; vitamin b12; holotranscobalamin; methylmalonic acid Gene Set From GAD Gene-Disease Associations genes associated with the disease homocysteine; vitamin b12; holotranscobalamin; methylmalonic acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bsmi vitamin d receptor gene polymorphism Gene Set From GAD Gene-Disease Associations genes associated with the disease bsmi vitamin d receptor gene polymorphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; phenylketonurias; vitamin b deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; phenylketonurias; vitamin b deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; gastritis, atrophic; nervous system diseases; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; gastritis, atrophic; nervous system diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folate pathway vitamin levels Gene Set From GAD Gene-Disease Associations genes associated with the disease folate pathway vitamin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin c excretion Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin c excretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
kidney diseases; vitamin a deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease kidney diseases; vitamin a deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
homocysteine; vitamin b12; transcobalamin Gene Set From GAD Gene-Disease Associations genes associated with the disease homocysteine; vitamin b12; transcobalamin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin a Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone resorption; vitamin k deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease bone resorption; vitamin k deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; vitamin d deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; vascular diseases; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; vascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
homocystinuria; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease homocystinuria; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin e Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin e in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin d Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin d in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin k Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin k in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
plasma level of vitamin b12 Gene Set From GAD Gene-Disease Associations genes associated with the disease plasma level of vitamin b12 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin d deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamin Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term vitamin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
vitamin a_rattus norvegicus_gpl85_gds238 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the vitamin a_rattus norvegicus_gpl85_gds238 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
vitamin c_mus musculus_gpl6246_gse19378 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the vitamin c_mus musculus_gpl6246_gse19378 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
vitamin c_mus musculus_gpl6246_gse19377 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the vitamin c_mus musculus_gpl6246_gse19377 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
vitamin c_homo sapiens_gpl6884_gse16590 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the vitamin c_homo sapiens_gpl6884_gse16590 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
vitamin e_mus musculus_gpl1261_gse42813 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the vitamin e_mus musculus_gpl1261_gse42813 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
vitamin c_homo sapiens_gpl570_gds3635 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the vitamin c_homo sapiens_gpl570_gds3635 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
vitamin a_rattus norvegicus_gpl85_gse3420 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the vitamin a_rattus norvegicus_gpl85_gse3420 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
vitamin c_homo sapiens_gpl570_gse11919 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the vitamin c_homo sapiens_gpl570_gse11919 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
vitamin c_mus musculus_gpl6246_gse32994 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the vitamin c_mus musculus_gpl6246_gse32994 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
vitamin c_mus musculus_gpl1261_gse37676 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the vitamin c_mus musculus_gpl1261_gse37676 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
regulation of vitamin d receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of vitamin d receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
water-soluble vitamin biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the water-soluble vitamin biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin a import Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin a import biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to vitamin Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to vitamin biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin d3 metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin d3 metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of vitamin d 24-hydroxylase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of vitamin d 24-hydroxylase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin b6 metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin b6 metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
response to vitamin Gene Set From GO Biological Process Annotations 2015 genes participating in the response to vitamin biological process from the curated GO Biological Process Annotations 2015 dataset.
fat-soluble vitamin catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the fat-soluble vitamin catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
fat-soluble vitamin biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the fat-soluble vitamin biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin d catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin d catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin a transport Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin a transport biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin d biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin d biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin k biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin k biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of vitamin metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of vitamin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
fat-soluble vitamin metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the fat-soluble vitamin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
response to vitamin b1 Gene Set From GO Biological Process Annotations 2015 genes participating in the response to vitamin b1 biological process from the curated GO Biological Process Annotations 2015 dataset.
response to vitamin b6 Gene Set From GO Biological Process Annotations 2015 genes participating in the response to vitamin b6 biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin e biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin e biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
response to vitamin b2 Gene Set From GO Biological Process Annotations 2015 genes participating in the response to vitamin b2 biological process from the curated GO Biological Process Annotations 2015 dataset.
response to vitamin b3 Gene Set From GO Biological Process Annotations 2015 genes participating in the response to vitamin b3 biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of vitamin d biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of vitamin d biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of vitamin a metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of vitamin a metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
water-soluble vitamin metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the water-soluble vitamin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of vitamin metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of vitamin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin transmembrane transport Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin k metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin k metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin a biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin a biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin k catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin k catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of vitamin metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of vitamin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin d receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin d receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of vitamin d biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of vitamin d biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of vitamin d receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of vitamin d receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin b6 biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin b6 biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of vitamin d receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of vitamin d receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin a metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin a metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin d metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin d metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to vitamin d Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to vitamin d biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to vitamin e Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to vitamin e biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to vitamin k Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to vitamin k biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin transport Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin transport biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of vitamin d biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of vitamin d biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
response to vitamin a Gene Set From GO Biological Process Annotations 2015 genes participating in the response to vitamin a biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to vitamin b1 Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to vitamin b1 biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of vitamin d 24-hydroxylase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of vitamin d 24-hydroxylase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin e metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the vitamin e metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
response to vitamin k Gene Set From GO Biological Process Annotations 2015 genes participating in the response to vitamin k biological process from the curated GO Biological Process Annotations 2015 dataset.
response to vitamin e Gene Set From GO Biological Process Annotations 2015 genes participating in the response to vitamin e biological process from the curated GO Biological Process Annotations 2015 dataset.
response to vitamin d Gene Set From GO Biological Process Annotations 2015 genes participating in the response to vitamin d biological process from the curated GO Biological Process Annotations 2015 dataset.
vitamin binding Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin e binding Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin e binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin d receptor activator activity Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin d receptor activator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin d receptor binding Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin d receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin d 24-hydroxylase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin d 24-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin d3 25-hydroxylase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin d3 25-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin d response element binding Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin d response element binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin d binding Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin d binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin-k-epoxide reductase (warfarin-sensitive) activity Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin-k-epoxide reductase (warfarin-sensitive) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin d 25-hydroxylase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the vitamin d 25-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
vitamin D3 Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the vitamin D3 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
vitamin K2 Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the vitamin K2 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
Response to Vitamin E supplementation Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to Vitamin E supplementation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Vitamin E levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Vitamin E levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Vitamin B12 levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Vitamin B12 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Vitamin D insufficiency Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Vitamin D insufficiency phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Vitamin D levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Vitamin D levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Serum vitamin D-binding protein levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Serum vitamin D-binding protein levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Folate pathway vitamin levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Folate pathway vitamin levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
vitamin b12 deficiency Gene Set From GWASdb SNP-Disease Associations genes associated with the disease vitamin b12 deficiency in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
vitamin metabolic disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease vitamin metabolic disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of vitamin metabolism Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of vitamin d metabolism Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of vitamin a metabolism Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of vitamin b metabolism Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
vitamin e deficiency Gene Set From GWASdb SNP-Phenotype Associations genes associated with the vitamin e deficiency phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the vitamin b12 metabolism Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of vitamin e metabolism Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
Vitamin K1 2,3-epoxide Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Vitamin K1 2,3-epoxide metabolite from the curated HMDB Metabolites of Enzymes dataset.
Vitamin K1 Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Vitamin K1 metabolite from the curated HMDB Metabolites of Enzymes dataset.
Vitamin K2 Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Vitamin K2 metabolite from the curated HMDB Metabolites of Enzymes dataset.
Reduced Vitamin K (phylloquinone) Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Reduced Vitamin K (phylloquinone) metabolite from the curated HMDB Metabolites of Enzymes dataset.
Vitamin D2 3-glucuronide Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Vitamin D2 3-glucuronide metabolite from the curated HMDB Metabolites of Enzymes dataset.
Vitamin D3 Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Vitamin D3 metabolite from the curated HMDB Metabolites of Enzymes dataset.
Vitamin A Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Vitamin A metabolite from the curated HMDB Metabolites of Enzymes dataset.
vitamin b6 deficiency Gene Set From HPO Gene-Disease Associations genes associated with the vitamin b6 deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vitamin b12 deficiency Gene Set From HPO Gene-Disease Associations genes associated with the vitamin b12 deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vitamin k deficiency Gene Set From HPO Gene-Disease Associations genes associated with the vitamin k deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of vitamin k metabolism Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of vitamin k metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of vitamin e metabolism Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of vitamin e metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of vitamin d metabolism Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of vitamin d metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vitamin d deficiency Gene Set From HPO Gene-Disease Associations genes associated with the vitamin d deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
malabsorption of vitamin b12 Gene Set From HPO Gene-Disease Associations genes associated with the malabsorption of vitamin b12 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of vitamin metabolism Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of vitamin metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of vitamin b metabolism Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of vitamin b metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the vitamin b12 metabolism Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the vitamin b12 metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vitamin e deficiency Gene Set From HPO Gene-Disease Associations genes associated with the vitamin e deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Vitamin K Deficiency Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vitamin K Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vitamin B 12 Deficiency Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vitamin B 12 Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vitamin A Deficiency Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vitamin A Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vitamin D Deficiency Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vitamin D Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vitamin B Deficiency Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vitamin B Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vitamin B12-dependent methionine synthase, activation domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vitamin B12-dependent methionine synthase, activation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Xanthine/uracil/vitamin C permease Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Xanthine/uracil/vitamin C permease protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cobalamin (vitamin B12)-binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cobalamin (vitamin B12)-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cobalamin (vitamin B12) biosynthesis CobW-like, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cobalamin (vitamin B12) biosynthesis CobW-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thiamin pyrophosphokinase, vitamin B1-binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamin pyrophosphokinase, vitamin B1-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vitamin D receptor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vitamin D receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cobalamin (vitamin B12)-dependent enzyme, catalytic Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cobalamin (vitamin B12)-dependent enzyme, catalytic protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cobalamin (vitamin B12)-binding transporter, eukaryotic Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cobalamin (vitamin B12)-binding transporter, eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vitamin K epoxide reductase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vitamin K epoxide reductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vitamin D binding protein, domain III Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vitamin D binding protein, domain III protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vitamin D-binding protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vitamin D-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cobalamin (vitamin B12)-binding module, cap domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cobalamin (vitamin B12)-binding module, cap domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cobalamin (vitamin B12)-dependent enzyme, catalytic subdomain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cobalamin (vitamin B12)-dependent enzyme, catalytic subdomain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vitamin K-dependent gamma-carboxylase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vitamin K-dependent gamma-carboxylase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Pyridoxal phosphate (active vitamin B6) biosynthesis, pyridoxal kinase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Pyridoxal phosphate (active vitamin B6) biosynthesis, pyridoxal kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
vitamin b6 metabolism Gene Set From KEGG Pathways proteins participating in the vitamin b6 metabolism pathway from the KEGG Pathways dataset.
abnormal vitamin absorption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vitamin d level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vitamin d level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vitamin b12 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin b12 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vitamin d level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin d level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vitamin metabolism Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vitamin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vitamin a metabolism Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin a metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vitamin c level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin c level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fat-soluble vitamin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fat-soluble vitamin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vitamin a level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin a level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vitamin e level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin e level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vitamin homeostasis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vitamin k-dependent clotting factors, combined deficiency of, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the vitamin k-dependent clotting factors, combined deficiency of, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
vitamin k-dependent clotting factors, combined deficiency of, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the vitamin k-dependent clotting factors, combined deficiency of, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia with isolated vitamin e deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia with isolated vitamin e deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
{vitamin b12 plasma level qtl1} Gene Set From OMIM Gene-Disease Associations genes associated with the {vitamin b12 plasma level qtl1} phenotype from the curated OMIM Gene-Disease Associations dataset.
methylmalonic aciduria, vitamin b12-responsive Gene Set From OMIM Gene-Disease Associations genes associated with the methylmalonic aciduria, vitamin b12-responsive phenotype from the curated OMIM Gene-Disease Associations dataset.
{vitamin b6 plasma level qtl 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {vitamin b6 plasma level qtl 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
rickets, vitamin d-resistant, type iia Gene Set From OMIM Gene-Disease Associations genes associated with the rickets, vitamin d-resistant, type iia phenotype from the curated OMIM Gene-Disease Associations dataset.
vitamin d-dependent rickets, type i Gene Set From OMIM Gene-Disease Associations genes associated with the vitamin d-dependent rickets, type i phenotype from the curated OMIM Gene-Disease Associations dataset.
rickets due to defect in vitamin d 25-hydroxylation Gene Set From OMIM Gene-Disease Associations genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset.
methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set From OMIM Gene-Disease Associations genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.
Vitamin B6 metabolism Gene Set From PANTHER Pathways proteins participating in the Vitamin B6 metabolism pathway from the PANTHER Pathways dataset.
Vitamin D (calciferol) metabolism Gene Set From Reactome Pathways 2014 proteins participating in the Vitamin D (calciferol) metabolism pathway from the Reactome Pathways dataset.
Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B) pathway from the Reactome Pathways dataset.
Vitamin C (ascorbate) metabolism Gene Set From Reactome Pathways 2014 proteins participating in the Vitamin C (ascorbate) metabolism pathway from the Reactome Pathways dataset.
Vitamin B2 (riboflavin) metabolism Gene Set From Reactome Pathways 2014 proteins participating in the Vitamin B2 (riboflavin) metabolism pathway from the Reactome Pathways dataset.
Vitamin B1 (thiamin) metabolism Gene Set From Reactome Pathways 2014 proteins participating in the Vitamin B1 (thiamin) metabolism pathway from the Reactome Pathways dataset.
Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A) pathway from the Reactome Pathways dataset.
Vitamin B5 (pantothenate) metabolism Gene Set From Reactome Pathways 2014 proteins participating in the Vitamin B5 (pantothenate) metabolism pathway from the Reactome Pathways dataset.
Vitamin D Metabolism(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Vitamin D Metabolism(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Vitamin B12 Metabolism(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Vitamin B12 Metabolism(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Vitamin A Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin A Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin B 12 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin B 12 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin D Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin D Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin D-Dependent Rickets Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin D-Dependent Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin K Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin K Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin B Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin B Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin B 6 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin B 6 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin E Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin E Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Deficiency Of Vitamin D3 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Deficiency Of Vitamin D3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin D-Resistant Rickets Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin D-Resistant Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin D Hydroxylation-Deficient Rickets, Type 1B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin D Hydroxylation-Deficient Rickets, Type 1B 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.
Vitamin K-Dependent Clotting Factors, Combined Deficiency Of Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin K-Dependent Clotting Factors, Combined Deficiency Of in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disorder Of Vitamin B12 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disorder Of Vitamin B12 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin D Dependent Rickets 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin D Dependent Rickets 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteomalacia Due To Vitamin D Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Osteomalacia Due To Vitamin D Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin K Deficiency Bleeding Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitamin K Deficiency Bleeding in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitamin D Measurement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitamin D Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitamin D3 Measurement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitamin D3 Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitamin B6 Measurement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitamin B6 Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitamin B12 Measurement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitamin B12 Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Malabsorption Of Vitamin B12 Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Malabsorption Of Vitamin B12 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Vitamin B12 Level Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Vitamin B12 Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Vitamin B12 Metabolism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Vitamin B12 Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitamin K Assay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitamin K Assay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Vitamin D Metabolism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Vitamin D Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitamin E Assay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitamin E Assay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Vitamin A Metabolism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Vitamin A Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Vitamin E Metabolism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Vitamin E Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitamin A Measurement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitamin A Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitamin Measurement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitamin Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitamin B12 Plasma Level Quantitative Trait Locus 1 Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitamin B12 Plasma Level Quantitative Trait Locus 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Vitamin Metabolism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Vitamin Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
positive regulation of vitamin D 24-hydroxylase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of vitamin D 24-hydroxylase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
response to vitamin D Gene Set From GO Biological Process Annotations 2023 genes participating in the response to vitamin D biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin D metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin D metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of vitamin D receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of vitamin D receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of vitamin D biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of vitamin D biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of vitamin D receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of vitamin D receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin A metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin A metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of vitamin D biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of vitamin D biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin transport Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin transport biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to vitamin D Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to vitamin D biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin D catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin D catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin D receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin D receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin E metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin E metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin K metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin K metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin D3 metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin D3 metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin K catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin K catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of vitamin D receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of vitamin D receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to vitamin K Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to vitamin K biological process from the curated GO Biological Process Annotations 2023 dataset.
response to vitamin B6 Gene Set From GO Biological Process Annotations 2023 genes participating in the response to vitamin B6 biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin A biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin A biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin K biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin K biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin A import into cell Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin A import into cell biological process from the curated GO Biological Process Annotations 2023 dataset.
water-soluble vitamin metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the water-soluble vitamin metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of vitamin D 24-hydroxylase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of vitamin D 24-hydroxylase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
response to vitamin Gene Set From GO Biological Process Annotations 2023 genes participating in the response to vitamin biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin D biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin D biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
fat-soluble vitamin metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the fat-soluble vitamin metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
fat-soluble vitamin catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the fat-soluble vitamin catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of vitamin metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of vitamin metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of vitamin D biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of vitamin D biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of vitamin metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of vitamin metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to vitamin Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to vitamin biological process from the curated GO Biological Process Annotations 2023 dataset.
water-soluble vitamin catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the water-soluble vitamin catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
response to vitamin K Gene Set From GO Biological Process Annotations 2023 genes participating in the response to vitamin K biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of vitamin metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of vitamin metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
water-soluble vitamin biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the water-soluble vitamin biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin B6 catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin B6 catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
fat-soluble vitamin biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the fat-soluble vitamin biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin B6 biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin B6 biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
vitamin A transport Gene Set From GO Biological Process Annotations 2023 genes participating in the vitamin A transport biological process from the curated GO Biological Process Annotations 2023 dataset.
ABC-type vitamin B12 transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the ABC-type vitamin B12 transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
nuclear vitamin D receptor binding Gene Set From GO Molecular Function Annotations 2023 genes performing the nuclear vitamin D receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
vitamin D 24-hydroxylase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the vitamin D 24-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
vitamin D3 25-hydroxylase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the vitamin D3 25-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
vitamin D response element binding Gene Set From GO Molecular Function Annotations 2023 genes performing the vitamin D response element binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
vitamin D 25-hydroxylase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the vitamin D 25-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
vitamin-K-epoxide reductase (warfarin-sensitive) activity Gene Set From GO Molecular Function Annotations 2023 genes performing the vitamin-K-epoxide reductase (warfarin-sensitive) activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
vitamin-K-epoxide reductase (warfarin-insensitive) activity Gene Set From GO Molecular Function Annotations 2023 genes performing the vitamin-K-epoxide reductase (warfarin-insensitive) activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
vitamin D binding Gene Set From GO Molecular Function Annotations 2023 genes performing the vitamin D binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
vitamin D 23-hydroxylase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the vitamin D 23-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
decreased vitamin D level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased vitamin D level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vitamin E level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin E level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fat-soluble vitamin level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fat-soluble vitamin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vitamin D level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin D level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vitamin A level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin A level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vitamin C level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin C level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vitamin absorption Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vitamin A metabolism Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin A metabolism phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vitamin level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vitamin homeostasis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased vitamin D level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased vitamin D level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vitamin B12 level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin B12 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Vitamin D3 Gene Set From MW Enzyme Metabolite Associations interacting proteins for Vitamin D3 metabolite from the MW Gene Metabolite Associations dataset.
Vitamin D metabolism Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin D metabolism pathway from the WikiPathways Pathways 2024 dataset.
Vitamin B12 metabolism Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin B12 metabolism pathway from the WikiPathways Pathways 2024 dataset.
Vitamin D receptor pathway Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin D receptor pathway pathway from the WikiPathways Pathways 2024 dataset.
PI3K AKT mTOR vitamin D3 signaling Gene Set From WikiPathways Pathways 2024 proteins participating in the PI3K AKT mTOR vitamin D3 signaling pathway from the WikiPathways Pathways 2024 dataset.
Vitamin B12 disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin B12 disorders pathway from the WikiPathways Pathways 2024 dataset.
Vitamin D in inflammatory diseases Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin D in inflammatory diseases pathway from the WikiPathways Pathways 2024 dataset.
Vitamin D sensitive calcium signaling in depression Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin D sensitive calcium signaling in depression pathway from the WikiPathways Pathways 2024 dataset.
Non classical role of vitamin D Gene Set From WikiPathways Pathways 2024 proteins participating in the Non classical role of vitamin D pathway from the WikiPathways Pathways 2024 dataset.
Effect of intestinal microbiome on anticoagulant response of vitamin K antagonists Gene Set From WikiPathways Pathways 2024 proteins participating in the Effect of intestinal microbiome on anticoagulant response of vitamin K antagonists pathway from the WikiPathways Pathways 2024 dataset.
Metabolism of vitamin K Gene Set From Reactome Pathways 2024 proteins participating in the Metabolism of vitamin K pathway from the Reactome Pathways 2024 dataset.
Vitamin B1 (thiamin) metabolism Gene Set From Reactome Pathways 2024 proteins participating in the Vitamin B1 (thiamin) metabolism pathway from the Reactome Pathways 2024 dataset.
Vitamin B2 (riboflavin) metabolism Gene Set From Reactome Pathways 2024 proteins participating in the Vitamin B2 (riboflavin) metabolism pathway from the Reactome Pathways 2024 dataset.
Vitamin B5 (pantothenate) metabolism Gene Set From Reactome Pathways 2024 proteins participating in the Vitamin B5 (pantothenate) metabolism pathway from the Reactome Pathways 2024 dataset.
Vitamin B6 activation to pyridoxal phosphate Gene Set From Reactome Pathways 2024 proteins participating in the Vitamin B6 activation to pyridoxal phosphate pathway from the Reactome Pathways 2024 dataset.
Vitamin C (ascorbate) metabolism Gene Set From Reactome Pathways 2024 proteins participating in the Vitamin C (ascorbate) metabolism pathway from the Reactome Pathways 2024 dataset.
Vitamin D (calciferol) metabolism Gene Set From Reactome Pathways 2024 proteins participating in the Vitamin D (calciferol) metabolism pathway from the Reactome Pathways 2024 dataset.
Vitamin E Gene Set From Reactome Pathways 2024 proteins participating in the Vitamin E pathway from the Reactome Pathways 2024 dataset.
vitamin metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of vitamin D 24-hydroxylase activity Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of vitamin D 24-hydroxylase activity biological process from the curated GO Biological Process Annotations 2025 dataset.
response to vitamin D Gene Set From GO Biological Process Annotations 2025 genes participating in the response to vitamin D biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin D metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin D metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of vitamin D receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of vitamin D receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of vitamin D biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of vitamin D biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of vitamin D receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of vitamin D receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin A metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin A metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of vitamin D biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of vitamin D biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin transport Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin transport biological process from the curated GO Biological Process Annotations 2025 dataset.
cellular response to vitamin D Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to vitamin D biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin D catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin D catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin D receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin D receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin E metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin E metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin K metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin K metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin D3 metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin D3 metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin K catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin K catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of vitamin D receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of vitamin D receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
cellular response to vitamin K Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to vitamin K biological process from the curated GO Biological Process Annotations 2025 dataset.
response to vitamin B6 Gene Set From GO Biological Process Annotations 2025 genes participating in the response to vitamin B6 biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin A biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin A biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin K biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin K biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin A import into cell Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin A import into cell biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin B6 metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin B6 metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
water-soluble vitamin metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the water-soluble vitamin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
response to vitamin Gene Set From GO Biological Process Annotations 2025 genes participating in the response to vitamin biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin D biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin D biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
fat-soluble vitamin metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the fat-soluble vitamin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
fat-soluble vitamin catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the fat-soluble vitamin catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of vitamin metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of vitamin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of vitamin D biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of vitamin D biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin B6 transport Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin B6 transport biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of vitamin metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of vitamin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
cellular response to vitamin Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to vitamin biological process from the curated GO Biological Process Annotations 2025 dataset.
water-soluble vitamin catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the water-soluble vitamin catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
response to vitamin K Gene Set From GO Biological Process Annotations 2025 genes participating in the response to vitamin K biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of vitamin metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of vitamin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
water-soluble vitamin biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the water-soluble vitamin biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin B6 catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin B6 catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
fat-soluble vitamin biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the fat-soluble vitamin biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin B6 biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin B6 biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
vitamin A transport Gene Set From GO Biological Process Annotations 2025 genes participating in the vitamin A transport biological process from the curated GO Biological Process Annotations 2025 dataset.
ABC-type vitamin B12 transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the ABC-type vitamin B12 transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
nuclear vitamin D receptor binding Gene Set From GO Molecular Function Annotations 2025 genes performing the nuclear vitamin D receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
vitamin E binding Gene Set From GO Molecular Function Annotations 2025 genes performing the vitamin E binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
vitamin D 24-hydroxylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the vitamin D 24-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
vitamin D3 25-hydroxylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the vitamin D3 25-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
vitamin D response element binding Gene Set From GO Molecular Function Annotations 2025 genes performing the vitamin D response element binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
vitamin-K-epoxide reductase (warfarin-sensitive) activity Gene Set From GO Molecular Function Annotations 2025 genes performing the vitamin-K-epoxide reductase (warfarin-sensitive) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
vitamin-K-epoxide reductase (warfarin-insensitive) activity Gene Set From GO Molecular Function Annotations 2025 genes performing the vitamin-K-epoxide reductase (warfarin-insensitive) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
vitamin D binding Gene Set From GO Molecular Function Annotations 2025 genes performing the vitamin D binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
vitamin B6 binding Gene Set From GO Molecular Function Annotations 2025 genes performing the vitamin B6 binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
vitamin D 23-hydroxylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the vitamin D 23-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Vitamin metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Vitamin metabolic disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial isolated deficiency of vitamin E Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial isolated deficiency of vitamin E from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Vitamin B12 deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Vitamin B12 deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Vitamin D-dependent rickets Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Vitamin D-dependent rickets from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Vitamin D-dependent rickets Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitamin D-dependent rickets in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitamin K deficiency bleeding Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitamin K deficiency bleeding in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitamin metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitamin metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitamin B12 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitamin B12 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial isolated deficiency of vitamin E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial isolated deficiency of vitamin E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset vitamin B6-dependent epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset vitamin B6-dependent epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined deficiency of vitamin K-dependent clotting factors 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined deficiency of vitamin K-dependent clotting factors 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary combined deficiency of vitamin K-dependent clotting factors Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary combined deficiency of vitamin K-dependent clotting factors in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitamin D-dependent rickets type 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitamin D-dependent rickets type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined deficiency of vitamin K-dependent clotting factors 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined deficiency of vitamin K-dependent clotting factors 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitamin D-dependent rickets type 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitamin D-dependent rickets type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitamin D-dependent rickets type 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitamin D-dependent rickets type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitamin D-dependent rickets type 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitamin D-dependent rickets type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset vitamin B6-dependent epilepsy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset vitamin B6-dependent epilepsy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitamin K4_SW 1088 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_SW 1088 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_Hs 766T Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_Hs 766T drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_SW480 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_SW480 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_SK-MEL-2 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_SK-MEL-2 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_hTERT-HPNE Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_hTERT-HPNE drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_J82 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_J82 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_SW 900 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_SW 900 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_A498 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_A498 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_SHP-77 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_SHP-77 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_NCI-H2030 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_NCI-H2030 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_NCI-H460 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_NCI-H460 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_BT-474 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_BT-474 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_KATO III Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_KATO III drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_NCI-H1573 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_NCI-H1573 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_LS 180 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_LS 180 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_SW 1271 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_SW 1271 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_CFPAC-1 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_CFPAC-1 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_AsPC-1 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_AsPC-1 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_HepG2/C3A Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_HepG2/C3A drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_A549 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_A549 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_A-427 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_A-427 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_HCT15 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_HCT15 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_AN3 CA Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_AN3 CA drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_Panc 03.27 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_Panc 03.27 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_PANC-1 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_PANC-1 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_SNU-1 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_SNU-1 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_RKO Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_RKO drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_LOX-IMVI Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_LOX-IMVI drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_NCI-H661 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_NCI-H661 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_NCI-H596 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_NCI-H596 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_NCI-H2347 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_NCI-H2347 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_NCI-H2122 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_NCI-H2122 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_C-33 A Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_C-33 A drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_HS-578T Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_HS-578T drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_SNU-423 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_SNU-423 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_MIA PaCa-2 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_MIA PaCa-2 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_SW48 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_SW48 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_COLO 205 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_COLO 205 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_HEC-1-A Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_HEC-1-A drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_CHP-212 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_CHP-212 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_RPMI-7951 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_RPMI-7951 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_H4 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_H4 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_A-172 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_A-172 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_NCI-H23 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_NCI-H23 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_SW1417 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_SW1417 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_C32 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_C32 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_HT-29 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_HT-29 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_NCI-H1792 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_NCI-H1792 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_LoVo Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_LoVo drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin K4_HOP62 Gene Set From Tahoe Therapeutics Tahoe 100M Perturbation Atlas genes differentially expressed following the Vitamin K4_HOP62 drug perturbation from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset.
Vitamin D-dependent rickets Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vitamin D-dependent rickets phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Vitamin D hydroxylation-deficient rickets Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vitamin D hydroxylation-deficient rickets phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Vitamin K-dependent clotting factors Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vitamin K-dependent clotting factors phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial isolated deficiency of vitamin Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial isolated deficiency of vitamin phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 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.
Vitamin D levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vitamin D levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vitamin B12 levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vitamin B12 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate x maternal periconceptional vitamin use interaction (parent of origin effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate x maternal periconceptional vitamin use interaction (parent of origin effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vitamin B levels in ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vitamin B levels in ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Serum vitamin D-binding protein levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum vitamin D-binding protein levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vitamin levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vitamin levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vitamin D insufficiency Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vitamin D insufficiency phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Folate pathway vitamin levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Folate pathway vitamin levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vitamin E levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vitamin E levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to Vitamin E supplementation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to Vitamin E supplementation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate (maternal periconceptional vitamin use interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate (maternal periconceptional vitamin use interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Serum vitamin D-binding protein levels in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum vitamin D-binding protein levels in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bioavailable vitamin D levels in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bioavailable vitamin D levels in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vitamin C levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vitamin C levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vitamin B6 metabolism Gene Set From KEGG Pathways 2026 proteins participating in the Vitamin B6 metabolism pathway from the KEGG Pathways 2026 dataset.
VITAMIN A Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VITAMIN A drug from theDGIdb Drug Targets 2026 dataset.
VITAMIN K3 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VITAMIN K3 drug from theDGIdb Drug Targets 2026 dataset.
VITAMIN A COMPOUND Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VITAMIN A COMPOUND drug from theDGIdb Drug Targets 2026 dataset.
D VITAMIN Gene Set From DGIdb Drug Targets 2026 interacting proteins for the D VITAMIN drug from theDGIdb Drug Targets 2026 dataset.
VITAMIN B6 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VITAMIN B6 drug from theDGIdb Drug Targets 2026 dataset.
VITAMIN K Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VITAMIN K drug from theDGIdb Drug Targets 2026 dataset.
VITAMIN E ACETATE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VITAMIN E ACETATE drug from theDGIdb Drug Targets 2026 dataset.
VITAMIN A PALMITATE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VITAMIN A PALMITATE drug from theDGIdb Drug Targets 2026 dataset.
VITAMIN B12 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VITAMIN B12 drug from theDGIdb Drug Targets 2026 dataset.
VITAMIN K3H2 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VITAMIN K3H2 drug from theDGIdb Drug Targets 2026 dataset.
VITAMIN D3 ANALOGUE ILX23-7553 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VITAMIN D3 ANALOGUE ILX23-7553 drug from theDGIdb Drug Targets 2026 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.
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.
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.
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.
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.

Harmonizome 3.0

Vitamin A1 and A5 X pathways Gene Set

human cytomegalovirus and map kinase pathways Gene Set

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

Myometrial Relaxation and Contraction Pathways(Homo sapiens) Gene Set

Myometrial Relaxation and Contraction Pathways(Mus musculus) Gene Set

Trans sulfuration one carbon metabolism and related pathways Gene Set

Myometrial relaxation and contraction pathways Gene Set

Amplification and expansion of oncogenic pathways as metastatic traits Gene Set

Physico chemical features and toxicity associated pathways Gene Set

Factors and pathways affecting insulin like growth factor IGF1 Akt signaling Gene Set

Urea cycle and associated pathways Gene Set

Pathways of nucleic acid metabolism and innate immune sensing Gene Set

Cholesterol metabolism with Bloch and Kandutsch Russell pathways Gene Set

RAS and bradykinin pathways in COVID 19 Gene Set

Proline and hydroxyproline pathways Gene Set

7 oxo C and 7 beta HC pathways Gene Set

Relevant molecular pathways and targeted agents in triple negative breast cancer Gene Set

ADHD and autism ASD pathways Gene Set

SARS-CoV-1 targets host intracellular signalling and regulatory pathways Gene Set

SARS-CoV-2 targets host intracellular signalling and regulatory pathways Gene Set

abnormal vitamin or vitamin cofactor metabolism Gene Set

Vitamin D levels (dietary vitamin D intake interaction) Gene Set

regulation of map kinase pathways through dual specificity phosphatases Gene Set

multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation Gene Set

pathways Gene Set

ventricular preexcitation with multiple accessory pathways Gene Set

Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways Gene Set

NS1 Mediated Effects on Host Pathways Gene Set

Regulatory RNA pathways Gene Set

RIG-I/MDA5 mediated induction of IFN-alpha/beta pathways Gene Set

SIDS Susceptibility Pathways(Homo sapiens) Gene Set

SIDS Susceptibility Pathways(Mus musculus) Gene Set

ESC Pluripotency Pathways(Mus musculus) Gene Set

G Protein Signaling Pathways(Homo sapiens) Gene Set

Interferon type I signaling pathways(Homo sapiens) Gene Set

Signaling Pathways in Glioblastoma(Homo sapiens) Gene Set

G Protein Signaling Pathways(Mus musculus) Gene Set

Methylation Pathways(Homo sapiens) Gene Set

Endothelin Pathways(Homo sapiens) Gene Set

Ventricular Preexcitation With Multiple Accessory Pathways Gene Set

Endothelin pathways Gene Set

Common pathways underlying drug addiction Gene Set

NAD biosynthetic pathways Gene Set

Pathways affected in adenoid cystic carcinoma Gene Set

Hypothesized pathways in pathogenesis of cardiovascular disease Gene Set

Embryonic stem cell pluripotency pathways Gene Set

Clear cell renal cell carcinoma pathways Gene Set

Thiamine metabolic pathways Gene Set

Autosomal recessive osteopetrosis pathways Gene Set

Overlap between signal transduction pathways contributing to LMNA laminopathies Gene Set

DNA repair pathways full network Gene Set

Opioid receptor pathways Gene Set

Metabolic pathways of fibroblasts Gene Set

Affected pathways in Duchenne muscular dystrophy Gene Set

Cancer pathways Gene Set

GNAQ pathways in port wine stain Gene Set

Effect of omega 3 PUFA on Huntington 39 s disease pathways Gene Set

Methylation pathways Gene Set

Sudden infant death syndrome SIDS susceptibility pathways Gene Set

Bacterial Infection Pathways Gene Set

Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models Gene Set

NS1 Mediated Effects on Host Pathways Gene Set

Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways Gene Set

Parasitic Infection Pathways Gene Set

Viral Infection Pathways Gene Set

Signaling pathways regulating pluripotency of stem cells Gene Set

Pathways in cancer Gene Set

Pathways of neurodegeneration - multiple diseases Gene Set

Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set

Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant Gene Set

homocysteine, folate and vitamin b12 levels Gene Set

plasma folate vitamin b12 homocyst(e)ine and colorectal cancer risk Gene Set

vitamin e and carotenoids Gene Set

hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set

Vitamin D metabolism and pathway Gene Set

Metabolism of steroid hormones and vitamin D Gene Set

Defects in vitamin and cofactor metabolism Gene Set

Cobalamin (Cbl, vitamin B12) transport and metabolism Gene Set

Vitamin A and Carotenoid Metabolism(Homo sapiens) Gene Set