Name

plasma total homocysteine and folate concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma total homocysteine and folate concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

serum folate and serum total homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum folate and serum total homocysteine in GWAS and other genetic association datasets from the GAD 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.

increased plasma concentrations of total cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased plasma concentrations of total cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

homocysteine, total plasma, elevated Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocysteine, total plasma, elevated phenotype from the curated OMIM 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.

fasting total cholesterol and ldl-cholesterol concentrations only Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting total cholesterol and ldl-cholesterol concentrations only in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

red cell folate concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease red cell folate concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney transplant; folate; homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease kidney transplant; folate; homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; folate; homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction; folate; homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folate; homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folate; homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney failure, chronic; folate; homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease kidney failure, chronic; folate; homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol, hdl; insulin; folate; homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol, hdl; insulin; folate; homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased plasma triglyceride and lower high-density lipoprotein cholesterol concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased plasma triglyceride and lower high-density lipoprotein cholesterol concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma concentrations of fluoxetine and paroxetine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma concentrations of fluoxetine and paroxetine 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.

folic acid in plasma and red blood cell folate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid in plasma and red blood cell folate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma total and ldl-apolipoprotein b Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma total and ldl-apolipoprotein b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced plasma concentrations of repaglinide Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced plasma concentrations of repaglinide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high plasma concentrations of high density lipoprotein ch Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high plasma concentrations of high density lipoprotein ch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

imipramine plasma concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease imipramine plasma concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma concentrations of carvedilol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma concentrations of carvedilol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Plasma amyloid beta peptide concentrations (ABx-42) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma amyloid beta peptide concentrations (ABx-42) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Plasma amyloid beta peptide concentrations (ABx-40) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma amyloid beta peptide concentrations (ABx-40) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype 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.

plasma folate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma folate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma homocysteine level Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma homocysteine level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma levels of homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma levels of homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma homocysteine levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma homocysteine levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Plasma homocysteine levels (post-methionine load test) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma homocysteine levels (post-methionine load test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

homocysteine plasma level Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocysteine plasma level phenotype from the curated OMIM Gene-Disease Associations dataset.

decreased plasma total carnitine Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased plasma total carnitine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

serum estrogen and progesterone concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum estrogen and progesterone concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lower levels of serum folate and hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lower levels of serum folate and hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Metabolism of folate and pterines Gene Set

From Reactome Pathways

proteins participating in the Metabolism of folate and pterines pathway from the Reactome Pathways dataset.

Folate-Alcohol and Cancer Pathway(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Folate-Alcohol and Cancer Pathway(Homo sapiens) pathway from the Wikipathways Pathways dataset.

homocysteine, cholesterol and vascular endothelial function Gene Set

From GAD Gene-Disease Associations

genes associated with the disease homocysteine, cholesterol and vascular endothelial function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

homocysteine metabolism, cognition, and white matter lesions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease homocysteine metabolism, cognition, and white matter lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced cbs activity and elevated post-load homocysteine levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced cbs activity and elevated post-load homocysteine levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Degradation of cysteine and homocysteine Gene Set

From Reactome Pathways

proteins participating in the Degradation of cysteine and homocysteine pathway from the Reactome Pathways dataset.

serum potassium and total cholesterol levels but not Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum potassium and total cholesterol levels but not in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

serum total and ionized calcium concentration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum total and ionized calcium concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total cholesterol and ldl-cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total cholesterol and ldl-cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total energy intake and cytokine sleep factors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total energy intake and cytokine sleep factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total and low-density lipoprotein cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total and low-density lipoprotein cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.

high serum ige concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high serum ige concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high insulin concentrations in non-diabetic mexican ameri Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high insulin concentrations in non-diabetic mexican ameri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bdnf serum concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bdnf serum concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sphingolipid concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sphingolipid concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

uric acid concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease uric acid concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tenoxicam concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tenoxicam concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated sweat chloride concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated sweat chloride concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hormone concentrations in postmenopausal women Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hormone concentrations in postmenopausal women in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

serum concentrations of creatinine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum concentrations of creatinine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasminogen activator inhibitor-1 concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasminogen activator inhibitor-1 concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dopamine d2 receptor density; monoamine metabolite concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dopamine d2 receptor density; monoamine metabolite concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherogenic uric acid concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherogenic uric acid concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

serum androgen concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum androgen concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipid concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipid concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased serum glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased serum glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood tacrolimus concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood tacrolimus concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intermediate density lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intermediate density lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angiotensinogen concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angiotensinogen concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

concentrationsthese Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term concentrationsthese in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

concentrations Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term concentrations in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

concentrationsmg Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term concentrationsmg in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Cerebral folate deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral folate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital defect of folate absorption Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Folate Malabsorption, Hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Folate Malabsorption, Hereditary from the curated CTD Gene-Disease Associations dataset.

Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset.

Neural tube defect, folate-sensitive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neural tube defect, folate-sensitive from the curated CTD Gene-Disease Associations dataset.

folate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folate 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.

colorectal cancer; folate, erythrocyte Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal cancer; folate, erythrocyte in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folate; hyperhomocystinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folate; hyperhomocystinemia 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.

folate; homocystinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folate; homocystinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

longer telomeres at low folate nutritional status Gene Set

From GAD Gene-Disease Associations

genes associated with the disease longer telomeres at low folate nutritional status in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folate pool Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folate pool in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; folate; hyperhomocystinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; folate; hyperhomocystinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folate Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term folate in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations 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.

folate-dependent fragile site at xq28 Gene Set

From HPO Gene-Disease Associations

genes associated with the folate-dependent fragile site at xq28 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

folate-responsive megaloblastic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the folate-responsive megaloblastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

folate-unresponsive megaloblastic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the folate-unresponsive megaloblastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

folate transformations Gene Set

From HumanCyc Pathways

proteins participating in the folate transformations pathway from the HumanCyc Pathways dataset.

folate polyglutamylation Gene Set

From HumanCyc Pathways

proteins participating in the folate polyglutamylation pathway from the HumanCyc Pathways dataset.

Reduced folate carrier Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Reduced folate carrier protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Folate receptor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Folate receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Folate-sensitive fragile site protein Fra10Ac1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Folate-sensitive fragile site protein Fra10Ac1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Folate transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Folate transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Folate receptor-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Folate receptor-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

one carbon pool by folate Gene Set

From KEGG Pathways

proteins participating in the one carbon pool by folate pathway from the KEGG Pathways dataset.

folate biosynthesis Gene Set

From KEGG Pathways

proteins participating in the folate biosynthesis pathway from the KEGG Pathways dataset.

{spina bifida, folate-sensitive, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {spina bifida, folate-sensitive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

folate malabsorption, hereditary Gene Set

From OMIM Gene-Disease Associations

genes associated with the folate malabsorption, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset.

{neural tube defects, folate-sensitive, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {neural tube defects, folate-sensitive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration due to cerebral folate transport deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration due to cerebral folate transport deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Folate Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Folate Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Homocysteine Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Homocysteine from the curated CTD Gene-Chemical Interactions dataset.

homocysteine thiolactone Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical homocysteine thiolactone from the curated CTD Gene-Chemical Interactions dataset.

Homocysteine Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Homocysteine in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

S-(D-Carboxybutyl)-L-Homocysteine Gene Set

From DrugBank Drug Targets

interacting proteins for the S-(D-Carboxybutyl)-L-Homocysteine drug from the curated DrugBank Drug Targets dataset.

S-Adenosyl-L-Homocysteine Gene Set

From DrugBank Drug Targets

interacting proteins for the S-Adenosyl-L-Homocysteine drug from the curated DrugBank Drug Targets 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.

homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, coronary; homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis, coronary; homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count 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.

lung cancer; homocysteine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung cancer; homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism, venous; homocysteine; thromboembolism, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thromboembolism, venous; homocysteine; thromboembolism, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

homocysteine Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term homocysteine in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

positive regulation of homocysteine metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of homocysteine metabolic process biological process from the curated GO Biological Process Annotations dataset.

homocysteine biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the homocysteine biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

homocysteine metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the homocysteine metabolic process biological process from the curated GO Biological Process Annotations dataset.

homocysteine catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the homocysteine catabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of homocysteine metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of homocysteine metabolic process biological process from the curated GO Biological Process Annotations dataset.

s-methylmethionine-homocysteine s-methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the s-methylmethionine-homocysteine s-methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

betaine-homocysteine s-methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the betaine-homocysteine s-methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

homocysteine desulfhydrase activity Gene Set

From GO Molecular Function Annotations

genes performing the homocysteine desulfhydrase activity molecular function from the curated GO Molecular Function Annotations dataset.

s-adenosylmethionine-homocysteine s-methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the s-adenosylmethionine-homocysteine s-methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

Homocysteine levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Homocysteine levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormality of homocysteine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Homocysteine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Homocysteine metabolite from the curated HMDB Metabolites of Enzymes dataset.

abnormality of homocysteine metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of homocysteine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cysteine biosynthesis/homocysteine degradation (trans-sulfuration) Gene Set

From HumanCyc Pathways

proteins participating in the cysteine biosynthesis/homocysteine degradation (trans-sulfuration) pathway from the HumanCyc Pathways dataset.

S-adenosyl-L-homocysteine hydrolase, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the S-adenosyl-L-homocysteine hydrolase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

S-adenosyl-L-homocysteine hydrolase, NAD binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the S-adenosyl-L-homocysteine hydrolase, NAD binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Homocysteine S-methyltransferase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Homocysteine S-methyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Betaine-homocysteine S-methyltransferase, BHMT Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Betaine-homocysteine S-methyltransferase, BHMT protein domain from the InterPro Predicted Protein Domain Annotations dataset.

BRD-A57957888_N-Acetyl-DL-homocysteine Thiolactone_MCF7_6.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-A57957888_N-Acetyl-DL-homocysteine Thiolactone_MCF7_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

abnormal circulating homocysteine level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating homocysteine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Cysteine formation from homocysteine Gene Set

From Reactome Pathways

proteins participating in the Cysteine formation from homocysteine pathway from the Reactome Pathways dataset.

Kininogen deficiency, total Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Kininogen deficiency, total phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, nuclear total Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, nuclear total phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

cholesterol, ldl; cholesterol, total; apolipoproteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; cholesterol, total; apolipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total serum ige. atopic dermatitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total serum ige. atopic dermatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; cholesterol, ldl; cholesterol, total; apoa1; apoe; apob-100 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; cholesterol, ldl; cholesterol, total; apoa1; apoe; apob-100 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol, ldl; cholesterol, total; insulin; apob Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol, ldl; cholesterol, total; insulin; apob in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atopy (total & specific ige) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atopy (total & specific ige) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total ige. eosinophilia. drs Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total ige. eosinophilia. drs in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total serum ige Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total serum ige in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, total Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, total in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; cholesterol, ldl; cholesterol, total; insulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; cholesterol, ldl; cholesterol, total; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total ige. spt. fev1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total ige. spt. fev1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; cholesterol, total Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; cholesterol, total in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; coronary heart disease; cholesterol, ldl; cholesterol, total Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; coronary heart disease; cholesterol, ldl; cholesterol, total in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

triglycerides; cholesterol, total; apoa1; apob; apoe Gene Set

From GAD Gene-Disease Associations

genes associated with the disease triglycerides; cholesterol, total; apoa1; apob; apoe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma. total serum ige Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma. total serum ige in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; cholesterol, total; insulin; cortisol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; cholesterol, total; insulin; cortisol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose; stroke; carotid artery intima-media thickness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose; stroke; carotid artery intima-media thickness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; cholesterol, total; insulin sensitivity; hyperinsulinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; cholesterol, total; insulin sensitivity; hyperinsulinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; dysplastic nevi; nevi, total Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; dysplastic nevi; nevi, total in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; cholesterol, total; apob; apoai Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; cholesterol, total; apob; apoai in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total serum ige. specific ige. ar Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total serum ige. specific ige. ar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total ige Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total ige in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma. bhr. total ige. spt Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma. bhr. total ige. spt in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total serum calcium Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total serum calcium in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total serum ige levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total serum ige levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; cholesterol, total; lipoprotein Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; cholesterol, total; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma. total ige Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma. total ige in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; cholesterol, total; c-reactive protein; apoa2; apob Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; cholesterol, total; c-reactive protein; apoa2; apob in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high total ige Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high total ige in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; cholesterol, total Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; cholesterol, total in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term total in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Serum total protein level Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Serum total protein level phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Response to protease inhibitor treatment in hepatitis c (peak serum total bilirubin levels) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to protease inhibitor treatment in hepatitis c (peak serum total bilirubin levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (paediatric, total body less head) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, total body less head) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Cholesterol, total Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Cholesterol, total phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Total ventricular volume Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Total ventricular volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

total cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the total cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased total bilirubin Gene Set

From HPO Gene-Disease Associations

genes associated with the increased total bilirubin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

total anomalous pulmonary venous return Gene Set

From HPO Gene-Disease Associations

genes associated with the total anomalous pulmonary venous return phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

total anomalous pulmonary venous connection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the total anomalous pulmonary venous connection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased circulating total protein level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased circulating total protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased total retina thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased total retina thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal total lung capacity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal total lung capacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased total retina thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased total retina thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

total anomalous pulmonary venous connection, intracardiac Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the total anomalous pulmonary venous connection, intracardiac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased circulating total protein level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased circulating total protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased total fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased total fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal total tissue mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal total tissue mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased total body fat amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased total body fat amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased total tissue mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased total tissue mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased total tissue mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased total tissue mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

total cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the total cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased total lung capacity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased total lung capacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased total fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased total fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal circulating total protein level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating total protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased total lung capacity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased total lung capacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal total fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal total fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal total retina thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal total retina thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased total body fat amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased total body fat amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

total anomalous pulmonary venous return Gene Set

From OMIM Gene-Disease Associations

genes associated with the total anomalous pulmonary venous return phenotype from the curated OMIM Gene-Disease Associations dataset.

reduced gene expression and lower plasma levels of beta2-glycoprotein i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced gene expression and lower plasma levels of beta2-glycoprotein i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma glucose, basal hepatic glucose and increased insulin release Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma glucose, basal hepatic glucose and increased insulin release in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma high density lipoprotein cholesterol and apolipoprotein ai Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma high density lipoprotein cholesterol and apolipoprotein ai in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma protein c levels and thrombotic risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma protein c levels and thrombotic risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma triglyceride and c-reactive protein, fasting glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma triglyceride and c-reactive protein, fasting glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma apob and low density lipoprotein (ldl) cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma apob and low density lipoprotein (ldl) cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma lipid and apolipoprotein levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma lipid and apolipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease. plasma lipoproteins. and longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease. plasma lipoproteins. and longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma cholesterol levels and drug response Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma cholesterol levels and drug response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma renin and prorenin levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma renin and prorenin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma lipid levels and body mass index Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma lipid levels and body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma fibrinogen levels in smokers and non-smokers Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma fibrinogen levels in smokers and non-smokers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease and plasma soluble thrombomodulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease and plasma soluble thrombomodulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma cholesterol levels and body mass index Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma cholesterol levels and body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aalpha and gamma fibrinogen plasma levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aalpha and gamma fibrinogen plasma levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lower plasma triglyceride levels and increased promoter activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lower plasma triglyceride levels and increased promoter activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease and plasma lipid levels. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease and plasma lipid levels. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

decreased blood pressure and plasma triglycerides Gene Set

From GAD Gene-Disease Associations

genes associated with the disease decreased blood pressure and plasma triglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipoproteins and plasma lipids Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipoproteins and plasma lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma factor vii activity and antigen levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma factor vii activity and antigen levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated plasma prothrombin levels and an increase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated plasma prothrombin levels and an increase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma apolipoprotein ai (apoai) and high-density lipoprotein cholesterol (hdl) levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma apolipoprotein ai (apoai) and high-density lipoprotein cholesterol (hdl) levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma carotenoid and tocopherol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma carotenoid and tocopherol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

quantitative variation in plasma high-density lipoproteins and triacylglycerides Gene Set

From GAD Gene-Disease Associations

genes associated with the disease quantitative variation in plasma high-density lipoproteins and triacylglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Response to serotonin reuptake inhibitors in major depressive disorder (plasma drug and metabolite levels) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to serotonin reuptake inhibitors in major depressive disorder (plasma drug and metabolite levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

From Reactome Pathways

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.

plasma membrane part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the plasma membrane part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

basal plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the basal plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

anchored component of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the anchored component of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of the cytoplasmic side of the plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of the cytoplasmic side of the plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extrinsic component of external side of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extrinsic component of external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

plasma lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the plasma lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

anchored component of external side of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the anchored component of external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

protein c inhibitor-plasma kallikrein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the protein c inhibitor-plasma kallikrein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

apicolateral plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the apicolateral plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

spanning component of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the spanning component of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of external side of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extrinsic component of cytoplasmic side of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extrinsic component of cytoplasmic side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

plasma membrane region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the plasma membrane region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extrinsic component of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extrinsic component of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

apical plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the apical plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of external side of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

plasma membrane raft Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the plasma membrane raft cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

basolateral plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the basolateral plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cytoplasmic side of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cytoplasmic side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

lateral plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the lateral plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

external side of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

plasma membrane Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores

proteins localized to the plasma membrane cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.

plasma membrane part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma membrane part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

basal plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the basal plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plasma membrane-derived chromatophore Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma membrane-derived chromatophore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

anchored component of plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the anchored component of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

yolk plasma Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the yolk plasma cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plasma lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plasma membrane respiratory chain Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma membrane respiratory chain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

apicolateral plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the apicolateral plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

spanning component of plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the spanning component of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

intrinsic component of plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the intrinsic component of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

integral component of plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the integral component of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

extrinsic component of cytoplasmic side of plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the extrinsic component of cytoplasmic side of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plasma membrane region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma membrane region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

extrinsic component of plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the extrinsic component of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

apical plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the apical plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plasma membrane raft Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma membrane raft cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plasma membrane-derived chromatophore membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma membrane-derived chromatophore membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plasma membrane light-harvesting complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma membrane light-harvesting complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

basolateral plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the basolateral plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cytoplasmic side of plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cytoplasmic side of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

lateral plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the lateral plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

external side of plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the external side of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Leukemia, Plasma Cell Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukemia, Plasma Cell from the curated CTD Gene-Disease Associations dataset.

Granuloma, Plasma Cell Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granuloma, Plasma Cell from the curated CTD Gene-Disease Associations dataset.

ZINC, ELEVATED PLASMA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ZINC, ELEVATED PLASMA from the curated CTD Gene-Disease Associations dataset.

Plasma Cell Granuloma, Pulmonary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Plasma Cell Granuloma, Pulmonary 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.

Serotonin Plasma Membrane Transport Proteins Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Serotonin Plasma Membrane Transport Proteins in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

plasma protein metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease plasma protein metabolism disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

pulmonary plasma cell granuloma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease pulmonary plasma cell granuloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

plasma protein metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease plasma protein metabolism disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

orbital plasma cell granuloma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease orbital plasma cell granuloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

plasma cell neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease plasma cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

plasma il6 levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma il6 levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure; aldosterone; glomerular filtration rate; renal plasma flow Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure; aldosterone; glomerular filtration rate; renal plasma flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma no metabolite levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma no metabolite levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma caffeine metabolite ratio Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma caffeine metabolite ratio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma vwf Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma vwf in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low plasma levels of factor viic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low plasma levels of factor viic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma glucose levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma glucose levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma endothelin-1 levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma endothelin-1 levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma chemerin levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma chemerin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

f12 plasma deficiency, moderate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease f12 plasma deficiency, moderate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high plasma cetp activity. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high plasma cetp activity. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma lipoproteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma lipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma lipid levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma lipid levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased plasma triglyceride levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased plasma triglyceride levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma fibrinogen levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma fibrinogen levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

differential plasma lipoprotein response to simvastatin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease differential plasma lipoprotein response to simvastatin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

specific levels of lp(a) in plasma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease specific levels of lp(a) in plasma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting plasma insulin levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting plasma insulin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting plasma glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting plasma glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma eosinophil count Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma eosinophil count in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased interleukin-10 (il-10) plasma levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased interleukin-10 (il-10) plasma levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high plasma factor viii: c levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high plasma factor viii: c levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high interleukin-1 beta plasma levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high interleukin-1 beta plasma levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma hdl-c levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma hdl-c levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma coagulation factors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma coagulation factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

serotonin plasma membrane transport proteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serotonin plasma membrane transport proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

haloperidol, plasma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haloperidol, plasma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma lp (a) levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma lp (a) levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma c4b binding protein levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma c4b binding protein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma lipoprotein(a) levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma lipoprotein(a) levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abt-773 plasma levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abt-773 plasma levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma high-density lipoprotein cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma high-density lipoprotein cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma levels of liver enzymes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma levels of liver enzymes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma factor xiii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma factor xiii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

igf1 plasma level Gene Set

From GAD Gene-Disease Associations

genes associated with the disease igf1 plasma level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

circadian variability in plasma pai-1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease circadian variability in plasma pai-1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

clozapine plasma levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease clozapine plasma levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma cell myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma cell myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma resistin levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma resistin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesteryl ester transfer protein plasma lipid levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesteryl ester transfer protein plasma lipid levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma hdl cholesterol (hdl-c) levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma hdl cholesterol (hdl-c) levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma protein c levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma protein c levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma il-6 levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma il-6 levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma lipid traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma lipid traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma adiponectin level Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma adiponectin level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma antigen levels of plasminogen activator inhibitor-1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma antigen levels of plasminogen activator inhibitor-1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased plasma leptin levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased plasma leptin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

variation in plasma lipoproteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease variation in plasma lipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma prothrombin levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma prothrombin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

interleukin-6 plasma level Gene Set

From GAD Gene-Disease Associations

genes associated with the disease interleukin-6 plasma level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma glucose concentration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma glucose concentration 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.

plasma lipoprotein traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma lipoprotein traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma hdl-cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma hdl-cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term plasma in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Osteolysis_Leukocyte - Lymphocyte - B-Lymphocyte - Plasma Cell (MMHCC)_GSE755 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Osteolysis_Leukocyte - Lymphocyte - B-Lymphocyte - Plasma Cell (MMHCC)_GSE755 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

protein localization to plasma membrane raft Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to plasma membrane raft biological process from the curated GO Biological Process Annotations dataset.

import across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the import across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

positive regulation of syncytium formation by plasma membrane fusion Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of syncytium formation by plasma membrane fusion biological process from the curated GO Biological Process Annotations dataset.

positive regulation of establishment of protein localization to plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of establishment of protein localization to plasma membrane biological process from the curated GO Biological Process Annotations dataset.

regulation of establishment of protein localization to plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the regulation of establishment of protein localization to plasma membrane biological process from the curated GO Biological Process Annotations dataset.

golgi to plasma membrane cftr protein transport Gene Set

From GO Biological Process Annotations

genes participating in the golgi to plasma membrane cftr protein transport biological process from the curated GO Biological Process Annotations dataset.

golgi to plasma membrane transport Gene Set

From GO Biological Process Annotations

genes participating in the golgi to plasma membrane transport biological process from the curated GO Biological Process Annotations dataset.

plasma membrane long-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

plasma membrane raft organization Gene Set

From GO Biological Process Annotations

genes participating in the plasma membrane raft organization biological process from the curated GO Biological Process Annotations dataset.

retrograde transport, endosome to plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the retrograde transport, endosome to plasma membrane biological process from the curated GO Biological Process Annotations dataset.

regulation of plasma cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of plasma cell differentiation biological process from the curated GO Biological Process Annotations dataset.

cell-cell adhesion via plasma-membrane adhesion molecules Gene Set

From GO Biological Process Annotations

genes participating in the cell-cell adhesion via plasma-membrane adhesion molecules biological process from the curated GO Biological Process Annotations dataset.

regulation of protein localization to plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein localization to plasma membrane biological process from the curated GO Biological Process Annotations dataset.

negative regulation of golgi to plasma membrane protein transport Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of golgi to plasma membrane protein transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of protein localization to plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of protein localization to plasma membrane biological process from the curated GO Biological Process Annotations dataset.

l-ornithine import across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the l-ornithine import across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

plasma lipoprotein particle assembly Gene Set

From GO Biological Process Annotations

genes participating in the plasma lipoprotein particle assembly biological process from the curated GO Biological Process Annotations dataset.

activation of plasma proteins involved in acute inflammatory response Gene Set

From GO Biological Process Annotations

genes participating in the activation of plasma proteins involved in acute inflammatory response biological process from the curated GO Biological Process Annotations dataset.

positive regulation of golgi to plasma membrane protein transport Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of golgi to plasma membrane protein transport biological process from the curated GO Biological Process Annotations dataset.

potassium ion import across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the potassium ion import across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

regulation of golgi to plasma membrane protein transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of golgi to plasma membrane protein transport biological process from the curated GO Biological Process Annotations dataset.

retrograde transport, plasma membrane to golgi Gene Set

From GO Biological Process Annotations

genes participating in the retrograde transport, plasma membrane to golgi biological process from the curated GO Biological Process Annotations dataset.

negative regulation of plasma lipoprotein particle oxidation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations dataset.

heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules Gene Set

From GO Biological Process Annotations

genes participating in the heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules biological process from the curated GO Biological Process Annotations dataset.

calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules Gene Set

From GO Biological Process Annotations

genes participating in the calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules biological process from the curated GO Biological Process Annotations dataset.

calcium ion import across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the calcium ion import across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

regulation of plasma membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of plasma membrane organization biological process from the curated GO Biological Process Annotations dataset.

sodium ion import across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the sodium ion import across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

negative regulation of establishment of protein localization to plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of establishment of protein localization to plasma membrane biological process from the curated GO Biological Process Annotations dataset.

regulation of plasma membrane long-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

protein targeting to plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein targeting to plasma membrane biological process from the curated GO Biological Process Annotations dataset.

regulation of plasma lipoprotein particle levels Gene Set

From GO Biological Process Annotations

genes participating in the regulation of plasma lipoprotein particle levels biological process from the curated GO Biological Process Annotations dataset.

plasma lipoprotein particle organization Gene Set

From GO Biological Process Annotations

genes participating in the plasma lipoprotein particle organization biological process from the curated GO Biological Process Annotations dataset.

cytoskeletal anchoring at plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the cytoskeletal anchoring at plasma membrane biological process from the curated GO Biological Process Annotations dataset.

negative regulation of syncytium formation by plasma membrane fusion Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of syncytium formation by plasma membrane fusion biological process from the curated GO Biological Process Annotations dataset.

positive regulation of potassium ion export across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of potassium ion export across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

maintenance of protein location in plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the maintenance of protein location in plasma membrane biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein localization to plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein localization to plasma membrane biological process from the curated GO Biological Process Annotations dataset.

plasma cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the plasma cell differentiation biological process from the curated GO Biological Process Annotations dataset.

fusion of sperm to egg plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the fusion of sperm to egg plasma membrane biological process from the curated GO Biological Process Annotations dataset.

l-arginine import across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the l-arginine import across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

plasma membrane raft assembly Gene Set

From GO Biological Process Annotations

genes participating in the plasma membrane raft assembly biological process from the curated GO Biological Process Annotations dataset.

potassium ion export across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the potassium ion export across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

regulation of plasma lipoprotein particle oxidation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations dataset.

plasma membrane fusion Gene Set

From GO Biological Process Annotations

genes participating in the plasma membrane fusion biological process from the curated GO Biological Process Annotations dataset.

fusion of virus membrane with host plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the fusion of virus membrane with host plasma membrane biological process from the curated GO Biological Process Annotations dataset.

plasma lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the plasma lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

plasma membrane lactate transport Gene Set

From GO Biological Process Annotations

genes participating in the plasma membrane lactate transport biological process from the curated GO Biological Process Annotations dataset.

calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules Gene Set

From GO Biological Process Annotations

genes participating in the calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules biological process from the curated GO Biological Process Annotations dataset.

syncytium formation by plasma membrane fusion Gene Set

From GO Biological Process Annotations

genes participating in the syncytium formation by plasma membrane fusion biological process from the curated GO Biological Process Annotations dataset.

plasma membrane to endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the plasma membrane to endosome transport biological process from the curated GO Biological Process Annotations dataset.

homophilic cell adhesion via plasma membrane adhesion molecules Gene Set

From GO Biological Process Annotations

genes participating in the homophilic cell adhesion via plasma membrane adhesion molecules biological process from the curated GO Biological Process Annotations dataset.

protein localization to plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to plasma membrane biological process from the curated GO Biological Process Annotations dataset.

plasma kallikrein-kinin cascade Gene Set

From GO Biological Process Annotations

genes participating in the plasma kallikrein-kinin cascade biological process from the curated GO Biological Process Annotations dataset.

positive regulation of plasma cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of plasma cell differentiation biological process from the curated GO Biological Process Annotations dataset.

plasma membrane repair Gene Set

From GO Biological Process Annotations

genes participating in the plasma membrane repair biological process from the curated GO Biological Process Annotations dataset.

regulation of potassium ion export across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the regulation of potassium ion export across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

protein transport into plasma membrane raft Gene Set

From GO Biological Process Annotations

genes participating in the protein transport into plasma membrane raft biological process from the curated GO Biological Process Annotations dataset.

golgi to plasma membrane protein transport Gene Set

From GO Biological Process Annotations

genes participating in the golgi to plasma membrane protein transport biological process from the curated GO Biological Process Annotations dataset.

regulation of fusion of sperm to egg plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the regulation of fusion of sperm to egg plasma membrane biological process from the curated GO Biological Process Annotations dataset.

regulation of golgi to plasma membrane cftr protein transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of golgi to plasma membrane cftr protein transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of golgi to plasma membrane cftr protein transport Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of golgi to plasma membrane cftr protein transport biological process from the curated GO Biological Process Annotations dataset.

amino acid import across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the amino acid import across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

protein localization to basolateral plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to basolateral plasma membrane biological process from the curated GO Biological Process Annotations dataset.

establishment of protein localization to plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the establishment of protein localization to plasma membrane biological process from the curated GO Biological Process Annotations dataset.

plasma membrane copper ion transport Gene Set

From GO Biological Process Annotations

genes participating in the plasma membrane copper ion transport biological process from the curated GO Biological Process Annotations dataset.

plasma lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the plasma lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

plasma lipoprotein particle oxidation Gene Set

From GO Biological Process Annotations

genes participating in the plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations dataset.

regulation of syncytium formation by plasma membrane fusion Gene Set

From GO Biological Process Annotations

genes participating in the regulation of syncytium formation by plasma membrane fusion biological process from the curated GO Biological Process Annotations dataset.

positive regulation of plasma membrane long-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of plasma membrane long-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

plasma membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the plasma membrane organization biological process from the curated GO Biological Process Annotations dataset.

l-lysine import across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the l-lysine import across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

plasma membrane part Gene Set

From GO Cellular Component Annotations

proteins localized to the plasma membrane part cellular component from the curated GO Cellular Component Annotations dataset.

basal plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the basal plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

anchored component of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the anchored component of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

protein c inhibitor-plasma kallikrein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the protein c inhibitor-plasma kallikrein complex cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of the cytoplasmic side of the plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of the cytoplasmic side of the plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

extrinsic component of external side of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the extrinsic component of external side of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

plasma lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the plasma lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

extrinsic component of cytoplasmic side of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the extrinsic component of cytoplasmic side of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

apicolateral plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the apicolateral plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

spanning component of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the spanning component of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

integral component of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of external side of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of external side of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

plasma membrane respiratory chain complex i Gene Set

From GO Cellular Component Annotations

proteins localized to the plasma membrane respiratory chain complex i cellular component from the curated GO Cellular Component Annotations dataset.

plasma membrane region Gene Set

From GO Cellular Component Annotations

proteins localized to the plasma membrane region cellular component from the curated GO Cellular Component Annotations dataset.

extrinsic component of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the extrinsic component of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

apical plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the apical plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

integral component of external side of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of external side of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

plasma membrane raft Gene Set

From GO Cellular Component Annotations

proteins localized to the plasma membrane raft cellular component from the curated GO Cellular Component Annotations dataset.

anchored component of external side of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the anchored component of external side of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

basolateral plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the basolateral plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

cytoplasmic side of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the cytoplasmic side of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

lateral plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the lateral plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

external side of plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the external side of plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

plasma membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the plasma membrane cellular component from the curated GO Cellular Component Annotations dataset.

Fasting plasma glucose Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting plasma glucose phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Stearic acid (18:0) plasma levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Stearic acid (18:0) plasma levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Circulating myeloperoxidase levels (plasma) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Circulating myeloperoxidase levels (plasma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Beta-2 microglubulin plasma levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Beta-2 microglubulin plasma levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Plasma omega-6 polyunsaturated fatty acid levels (linoleic acid) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma omega-6 polyunsaturated fatty acid levels (linoleic acid) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Plasma thyroid-stimulating hormone levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma thyroid-stimulating hormone levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Estradiol plasma levels (breast cancer) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Estradiol plasma levels (breast cancer) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Plasma omega-6 polyunsaturated fatty acid levels (arachidonic acid) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma omega-6 polyunsaturated fatty acid levels (arachidonic acid) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Palmitoleic acid (16:1n-7) plasma levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Palmitoleic acid (16:1n-7) plasma levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Phospholipid levels (plasma) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Phospholipid levels (plasma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Plasma omega-6 polyunsaturated fatty acid levels (adrenic acid) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma omega-6 polyunsaturated fatty acid levels (adrenic acid) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Plasma omega-6 polyunsaturated fatty acid levels (dihomo-gamma-linolenic acid) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma omega-6 polyunsaturated fatty acid levels (dihomo-gamma-linolenic acid) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Oleic acid (18:1n-9) plasma levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Oleic acid (18:1n-9) plasma levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

β2-Glycoprotein I (β2-GPI) plasma levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the β2-Glycoprotein I (β2-GPI) plasma levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Palmitic acid (16:0) plasma levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Palmitic acid (16:0) plasma levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Plasma plasminogen activator levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma plasminogen activator levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Plasma omega-6 polyunsaturated fatty acid levels (gamma-linolenic acid) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma omega-6 polyunsaturated fatty acid levels (gamma-linolenic acid) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

low plasma citrulline Gene Set

From HPO Gene-Disease Associations

genes associated with the low plasma citrulline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated plasma branched chain amino acids Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated plasma branched chain amino acids phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased plasma carnitine Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased plasma carnitine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased plasma free carnitine Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased plasma free carnitine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated plasma citrulline Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated plasma citrulline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated plasma pyrophosphate Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated plasma pyrophosphate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Leukemia, Plasma Cell Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leukemia, Plasma Cell phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Peptidase M43, pregnancy-associated plasma-A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase M43, pregnancy-associated plasma-A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Plasma membrane calcium-transporting ATPase 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasma membrane calcium-transporting ATPase 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Plasma membrane calcium-transporting ATPase 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasma membrane calcium-transporting ATPase 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Plasma membrane calcium-transporting ATPase 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasma membrane calcium-transporting ATPase 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Plasma membrane calcium-transporting ATPase 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasma membrane calcium-transporting ATPase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Plasma alpha-L-fucosidase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasma alpha-L-fucosidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Plasma membrane calcium transporting P-type ATPase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasma membrane calcium transporting P-type ATPase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Plasma protease C1 inhibitor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasma protease C1 inhibitor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

apical plasma membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the apical plasma membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

plasma membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the plasma membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

plasma membrane part Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the plasma membrane part cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

basolateral plasma membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the basolateral plasma membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

plasma membrane region Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the plasma membrane region cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

abnormal plasma membrane morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal plasma membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal plasma cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased plasma cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal plasma membrane sphingolipid content Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal plasma membrane sphingolipid content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal renal plasma flow rate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal renal plasma flow rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal plasma anion gap Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal plasma anion gap phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased plasma membrane sphingolipid content Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased plasma membrane sphingolipid content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal plasma cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal plasma cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased plasma cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent plasma cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent plasma cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased renal plasma flow rate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased renal plasma flow rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased plasma anion gap Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased plasma anion gap phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long lived plasma cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long lived plasma cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased renal plasma flow rate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased renal plasma flow rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal plasma cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal plasma cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

plasma triglyceride level qtl, low Gene Set

From OMIM Gene-Disease Associations

genes associated with the plasma triglyceride level qtl, low phenotype from the curated OMIM Gene-Disease Associations dataset.

{alkaline phosphatase, plasma level of, qtl4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alkaline phosphatase, plasma level of, qtl4} phenotype from the curated OMIM Gene-Disease Associations dataset.

plasma fibronectin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the plasma fibronectin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

[dopamine-beta-hydroxylase activity levels, plasma] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [dopamine-beta-hydroxylase activity levels, plasma] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 5] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 5] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 4] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 4] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 6] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 6] 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.

[fasting plasma glucose level qtl 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

[polyunsaturated fatty acids plasma level qtl1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [polyunsaturated fatty acids plasma level qtl1] 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.

[plasma glucose, 2-hour, qtl 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [plasma glucose, 2-hour, qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

{alkaline phosphatase, plasma level of, qtl1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alkaline phosphatase, plasma level of, qtl1} phenotype from the curated OMIM Gene-Disease Associations dataset.

[plasma glucose, 2-hour, qtl 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [plasma glucose, 2-hour, qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

{alkaline phosphatase, plasma level of, qtl3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alkaline phosphatase, plasma level of, qtl3} phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 3] phenotype from the curated OMIM Gene-Disease Associations dataset.

{alkaline phosphatase, plasma level of, qtl 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alkaline phosphatase, plasma level of, qtl 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

plasma Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term plasma in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Plasma membrane estrogen receptor signaling Gene Set

From PID Pathways

proteins participating in the Plasma membrane estrogen receptor signaling pathway from the PID Pathways dataset.

Transport of connexons to the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Transport of connexons to the plasma membrane pathway from the Reactome Pathways dataset.

Synthesis of PIPs at the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PIPs at the plasma membrane pathway from the Reactome Pathways dataset.

Translocation of GLUT4 to the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Translocation of GLUT4 to the plasma membrane pathway from the Reactome Pathways dataset.

MyD88 cascade initiated on plasma membrane Gene Set

From Reactome Pathways

proteins participating in the MyD88 cascade initiated on plasma membrane pathway from the Reactome Pathways dataset.

NGF signalling via TRKA from the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the NGF signalling via TRKA from the plasma membrane pathway from the Reactome Pathways dataset.

Scavenging of heme from plasma Gene Set

From Reactome Pathways

proteins participating in the Scavenging of heme from plasma pathway from the Reactome Pathways dataset.

Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane pathway from the Reactome Pathways dataset.

Anchoring of the basal body to the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Anchoring of the basal body to the plasma membrane pathway from the Reactome Pathways dataset.

Amino acid transport across the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Amino acid transport across the plasma membrane pathway from the Reactome Pathways dataset.

MyD88:Mal cascade initiated on plasma membrane Gene Set

From Reactome Pathways

proteins participating in the MyD88:Mal cascade initiated on plasma membrane pathway from the Reactome Pathways dataset.

seminal plasma Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue seminal plasma from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

plasma cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue plasma cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

blood plasma Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue blood plasma from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

blood plasma Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue blood plasma in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

seminal plasma Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue seminal plasma in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

plasma cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue plasma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

blood plasma Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue blood plasma in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

plasma membrane Gene Set

From LOCATE Predicted Protein Localization Annotations

proteins predicted to localize to the plasma membrane cellular component from the LOCATE Predicted Protein Localization Annotations 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.

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.

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

genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 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

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

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

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

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

proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.

Synthesis and processing of ENV and VPU Gene Set

From Reactome Pathways

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

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

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

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

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the Wikipathways Pathways dataset.

SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Basic cell groups and regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

head and face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

telomeres telomerase cellular aging and immortality Gene Set

From Biocarta Pathways

proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.

mcalpain and friends in cell motility Gene Set

From Biocarta Pathways

proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.

il12 and stat4 dependent signaling pathway in th1 development Gene Set

From Biocarta Pathways

proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.

hypoxia and p53 in the cardiovascular system Gene Set

From Biocarta Pathways

proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.

lissencephaly gene (lis1) in neuronal migration and development Gene Set

From Biocarta Pathways

proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.

role of erbb2 in signal transduction and oncology Gene Set

From Biocarta Pathways

proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.

corticosteroids and cardioprotection Gene Set

From Biocarta Pathways

proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.

cyclins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.

mechanism of acetaminophen activity and toxicity Gene Set

From Biocarta Pathways

proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.

nfat and hypertrophy of the heart Gene Set

From Biocarta Pathways

proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.

acetylation and deacetylation of rela in nucleus Gene Set

From Biocarta Pathways

proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.

thrombin signaling and protease-activated receptors Gene Set

From Biocarta Pathways

proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.

antigen processing and presentation Gene Set

From Biocarta Pathways

proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.

stathmin and breast cancer resistance to antimicrotubule agents Gene Set

From Biocarta Pathways

proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.

role of ß-arrestins in the activation and targeting of map kinases Gene Set

From Biocarta Pathways

proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.

cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.

role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set

From Biocarta Pathways

proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.

btg family proteins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.

control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.

endocytotic role of ndk phosphins and dynamin Gene Set

From Biocarta Pathways

proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.

regulation of eif-4e and p70s6 kinase Gene Set

From Biocarta Pathways

proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.

estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set

From Biocarta Pathways

proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.

vegf hypoxia and angiogenesis Gene Set

From Biocarta Pathways

proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.

yaci and bcma stimulation of b cell immune responses Gene Set

From Biocarta Pathways

proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.

lck and fyn tyrosine kinases in initiation of tcr activation Gene Set

From Biocarta Pathways

proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.

hiv-1 nef: negative effector of fas and tnf Gene Set

From Biocarta Pathways

proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.

nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set

From Biocarta Pathways

proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.

ucalpain and friends in cell spread Gene Set

From Biocarta Pathways

proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.

ionomycin and phorbal ester signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.

carm1 and regulation of the estrogen receptor Gene Set

From Biocarta Pathways

proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.

phosphoinositides and their downstream targets Gene Set

From Biocarta Pathways

proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.

melanocyte development and pigmentation pathway Gene Set

From Biocarta Pathways

proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.

akap95 role in mitosis and chromosome dynamics Gene Set

From Biocarta Pathways

proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.

transcription factor creb and its extracellular signals Gene Set

From Biocarta Pathways

proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.

visceral fat deposits and the metabolic syndrome Gene Set

From Biocarta Pathways

proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.

the igf-1 receptor and longevity Gene Set

From Biocarta Pathways

proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.

cdc25 and chk1 regulatory pathway in response to dna damage Gene Set

From Biocarta Pathways

proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.

human cytomegalovirus and map kinase pathways Gene Set

From Biocarta Pathways

proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.

influence of ras and rho proteins on g1 to s transition Gene Set

From Biocarta Pathways

proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.

proteolysis and signaling pathway of notch Gene Set

From Biocarta Pathways

proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.

apoptotic dna-fragmentation and tissue homeostasis Gene Set

From Biocarta Pathways

proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.

ion channels and their functional role in vascular endothelium Gene Set

From Biocarta Pathways

proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

fosb gene expression and drug abuse Gene Set

From Biocarta Pathways

proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.

links between pyk2 and map kinases Gene Set

From Biocarta Pathways

proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.

opposing roles of aif in apoptosis and cell survival Gene Set

From Biocarta Pathways

proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.

degradation of the rar and rxr by the proteasome Gene Set

From Biocarta Pathways

proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.

cadmium induces dna synthesis and proliferation in macrophages Gene Set

From Biocarta Pathways

proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.

erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set

From Biocarta Pathways

proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.

role of brca1 brca2 and atr in cancer susceptibility Gene Set

From Biocarta Pathways

proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.

chrebp regulation by carbohydrates and camp Gene Set

From Biocarta Pathways

proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.

pten dependent cell cycle arrest and apoptosis Gene Set

From Biocarta Pathways

proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.

induction of apoptosis through dr3 and dr4/5 death receptors Gene Set

From Biocarta Pathways

proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.

CIITA-18437201-Raji B cells and iDC-human Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

VDR-23401126-LCL-AND-THP1-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Hypothyroidism, central, and testicular enlargement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trifunctional protein deficiency with myopathy and neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and presenile cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, mental retardation, and seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vater association with macrocephaly and ventriculomegaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microtia, hearing impairment, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sinoatrial node dysfunction and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation with language impairment and autistic features Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple Cutaneous and Mucosal Venous Malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy hereditary sensory and autonomic type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anemia sideroblastic and spinocerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mullerian aplasia and hyperandrogenism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Knuckle pads, deafness AND leukonychia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multicentric osteolysis, nodulosis and arthropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stapes ankylosis with broad thumb and toes Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome and Noonan-related syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, short stature, and impaired glucose metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell and Lange-Nielsen syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination and Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy dilated with woolly hair and keratoderma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract and cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, microphthalmia and nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and anterior segment dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bone fragility with contractures, arterial rupture, and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ulna and fibula absence of with severe limb deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Factor v and factor viii, combined deficiency of, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary Paragangliomas and Pheochromocytomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Band-like calcification with simplified gyration and polymicrogyria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, epilepsy, and diabetes syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, juvenile, with microcornea and glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, deafness, and narcolepsy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile macular degeneration and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary leiomyomatosis and renal cell cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monocyte and dendritic cell deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, hiatal hernia and nephrotic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell and Lange-Nielsen syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined malonic and methylmalonic aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis Gyrata syndrome of Beare and Stevenson Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aniridia, cerebellar ataxia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hereditary motor and sensory neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniosynostosis and dental anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, hyperphagia, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebroretinal microangiopathy with calcifications and cysts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy and paroxysmal dyskinesia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alacrima, achalasia, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, normal intelligence and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Calcification of joints and arteries Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypotrichosis and recurrent skin vesicles Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutaneous telangiectasia and cancer syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pineal hyperplasia AND diabetes mellitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Morbid obesity and spermatogenic failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary sensory and autonomic neuropathy type IIA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopia, high, with cataract and vitreoretinal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of factor V and factor VIII, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Camptodactyly, tall stature, and hearing loss syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyogenic arthritis, pyoderma gangrenosum and acne Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth deficiency and mental retardation with facial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, cochlear, with myopia and intellectual impairment Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of sialidase AND beta galactosidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

calcium- and calmodulin-dependent protein kinase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mrna cleavage and polyadenylation specificity factor complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

calcium- and calmodulin-dependent protein kinase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mrna cleavage and polyadenylation specificity factor complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen and cuticulin-based cuticle extracellular matrix part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Set

From CORUM Protein Complexes

proteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset.

NRD complex (Nucleosome remodeling and deacetylation complex) Gene Set

From CORUM Protein Complexes

proteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset.

6S methyltransferase and RG-containing Sm proteins complex Gene Set

From CORUM Protein Complexes

proteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset.

Remodeling and spacing factor (RSF) complex Gene Set

From CORUM Protein Complexes

proteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset.

PBAF complex (Polybromo- and BAF containing complex) Gene Set

From CORUM Protein Complexes

proteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset.

Cleavage and polyadenylation factor (CPSF) Gene Set

From CORUM Protein Complexes

proteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset.

Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Set

From CORUM Protein Complexes

proteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Nucleic and chromatin Fanconi complex Gene Set

From CORUM Protein Complexes

proteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Set

From CORUM Protein Complexes

proteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset.

ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Set

From CORUM Protein Complexes

proteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.

20S methylosome and RG-containing Sm protein complex Gene Set

From CORUM Protein Complexes

proteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset.

Amino Acids, Peptides, and Proteins Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset.

Bile Acids and Salts Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset.

Prime and Bond NT Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset.

drospirenone and ethinyl estradiol combination Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset.

Hypophosphatemic Rickets And Hyperparathyroidism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset.

Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.

Synovitis granulomatous with uveitis and cranial neuropathies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.

Hereditary Sensory and Motor Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.

Preaxial deficiency, postaxial polydactyly and hypospadias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset.

Combined Cellular And Humoral Immune Defects With Granulomas Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.

OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset.

Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.

Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.

Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.

Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset.

Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset.

Microtia, Hearing Impairment, And Cleft Palate Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset.

OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset.

Acromegaloid features, overgrowth, cleft palate, and hernia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.

46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset.

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.

Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset.

Craniosynostosis, anal anomalies, and porokeratosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset.

Sacral defect and anterior sacral meningocele Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.

Classical Lissencephalies and Subcortical Band Heterotopias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Classical Lissencephalies and Subcortical Band Heterotopias from the curated CTD Gene-Disease Associations dataset.

Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 1 and deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.

Neuropathy, hereditary motor and sensory, Russe type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset.

Blepharophimosis, Ptosis, and Epicanthus Inversus Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blepharophimosis, Ptosis, and Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset.

Hypotrichosis And Recurrent Skin Vesicles Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.

Signs and Symptoms, Digestive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Signs and Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset.

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.

Methylmalonic Aciduria and Homocystinuria, CblD Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblD Type from the curated CTD Gene-Disease Associations dataset.

Head and Neck Neoplasms Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Head and Neck Neoplasms from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.

Cataract, Juvenile, With Microcornea And Glucosuria Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset.

HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset.

Venous Malformations, Multiple Cutaneous and Mucosal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset.

BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset.

Postoperative Nausea and Vomiting Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Postoperative Nausea and Vomiting from the curated CTD Gene-Disease Associations dataset.

Myopathy with lactic acidosis and sideroblastic anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.

Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset.

Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.

MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.

Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.

Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.

Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset.

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.

Hypopituitarism and septooptic 'dysplasia' Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset.

PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset.

Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset.

Aplasia of Lacrimal and Salivary Glands Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset.

Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset.

MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset.

Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset.

Calcification of Joints and Arteries Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Calcification of Joints and Arteries from the curated CTD Gene-Disease Associations dataset.

CHOANAL ATRESIA AND LYMPHEDEMA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHOANAL ATRESIA AND LYMPHEDEMA from the curated CTD Gene-Disease Associations dataset.

Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis from the curated CTD Gene-Disease Associations dataset.

Hereditary Motor And Sensory Neuropathy, Type IIC Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset.

Asthma, Nasal Polyps, And Aspirin Intolerance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Asthma, Nasal Polyps, And Aspirin Intolerance from the curated CTD Gene-Disease Associations dataset.

Neoplasms, Germ Cell and Embryonal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neoplasms, Germ Cell and Embryonal from the curated CTD Gene-Disease Associations dataset.

Hereditary Motor And Sensory Neuropathy VI Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset.

Cutis Gyrata Syndrome of Beare And Stevenson Gene Set