Name

THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.

plasminogen activator inhibitor-1; tissue-type plasminogen activator Gene Set

From GAD Gene-Disease Associations

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

hyperfibrinolysis, familial, due to increased release of plat Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperfibrinolysis, familial, due to increased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.

plasminogen activator; plasminogen activator inhibitor-type 1 Gene Set

From GAD Gene-Disease Associations

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

thrombophilia, familial, due to decreased release of plat Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, familial, due to decreased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.

Tissue Plasminogen Activator Gene Set

From dbGAP Gene-Trait Associations

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

tissue type plasminogen activator-regulated; secretion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tissue type plasminogen activator-regulated; secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tissue-type plasminogen activator levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tissue-type plasminogen activator levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tissue plasminogen activator Gene Set

From GAD Gene-Disease Associations

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

Tissue plasminogen activator Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tissue plasminogen activator protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Plasminogen activator inhibitor type 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Plasminogen activator inhibitor type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Plasminogen Activator Inhibitor-1 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Plasminogen Activator Inhibitor-1 Deficiency from the curated CTD Gene-Disease Associations dataset.

plasminogen activator Gene Set

From GAD Gene-Disease Associations

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

fibrinogen; factor vii; plasminogen activator inhibitor-1 Gene Set

From GAD Gene-Disease Associations

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

plasminogen activator; fibrinolytic activities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasminogen activator; fibrinolytic activities 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.

plasminogen activator inhibitor-1 Gene Set

From GAD Gene-Disease Associations

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

circulating levels of plasminogen activator inhibitor-1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease circulating levels of plasminogen activator inhibitor-1 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.

urokinase plasminogen activator signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the urokinase plasminogen activator signaling pathway biological process from the curated GO Biological Process Annotations dataset.

urokinase plasminogen activator receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the urokinase plasminogen activator receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

Plasminogen activator inhibitor type 1 levels (PAI-1) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasminogen activator inhibitor type 1 levels (PAI-1) 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.

Plasminogen activator inhibitor 1 RNA-binding protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasminogen activator inhibitor 1 RNA-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Plasminogen activator inhibitor-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasminogen activator inhibitor-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

{transcription of plasminogen activator inhibitor, modulator of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {transcription of plasminogen activator inhibitor, modulator of} phenotype from the curated OMIM Gene-Disease Associations dataset.

plasminogen activator inhibitor-1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the plasminogen activator inhibitor-1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Urokinase-type plasminogen activator (uPA) and uPAR-mediated signaling Gene Set

From PID Pathways

proteins participating in the Urokinase-type plasminogen activator (uPA) and uPAR-mediated signaling pathway from the PID Pathways dataset.

hyperfibrinolysis Gene Set

From GeneRIF Biological Term Annotations

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

Thrombophilia due to protein S deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to activated protein C resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to activated protein C resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to thrombomodulin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, X-Linked, Due To Factor Ix Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Thrombophilia Due To Elevated Histidine-Rich Glycoprotein Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia Due To Elevated Histidine-Rich Glycoprotein from the curated CTD Gene-Disease Associations dataset.

Thrombophilia due to Activated Protein C Resistance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia due to Activated Protein C Resistance from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

thrombophilia due to hrg deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to hrg deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to thrombomodulin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to heparin cofactor ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to heparin cofactor ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to activated protein c resistance Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to activated protein c resistance phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to elevated hrg Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to elevated hrg phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to antithrombin iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to antithrombin iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, x-linked, due to factor ix defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset.

{thrombophilia, susceptibility to, due to factor v leiden} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {thrombophilia, susceptibility to, due to factor v leiden} phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to thrombin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

decreased neurotransmitter release Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased neurotransmitter release phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased synaptic glutamate release Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased synaptic glutamate release phenotype in transgenic mice from the MPO Gene-Phenotype 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.

increased neurotransmitter release Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased neurotransmitter release phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Visceral adipose tissue/subcutaneous adipose tissue ratio Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Visceral adipose tissue/subcutaneous adipose tissue ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

decreased cervical spine flexion due to contractures of posterior cervical muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased sweating due to autonomic dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.

pseudohyperkalemia, familial, 2, due to red cell leak Gene Set

From OMIM Gene-Disease Associations

genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

goiter, familial, due to ttf-1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

decreased adipose tissue around neck Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased adipose tissue around neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of cytochrome c oxidase in muscle tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of cytochrome c oxidase in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased mitochondrial complex iii activity in liver tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased mitochondrial complex iii activity in liver tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased adipose tissue Gene Set

From HPO Gene-Disease Associations

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

decreased abdominal adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased abdominal adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased subcutaneous adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased subcutaneous adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased brown adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased brown adipose tissue amount 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.

decreased white adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased white adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased adipose tissue Gene Set

From HPO Gene-Disease Associations

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

increased connective tissue Gene Set

From HPO Gene-Disease Associations

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

increased facial adipose tissue Gene Set

From HPO Gene-Disease Associations

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

increased adipose tissue around the neck Gene Set

From HPO Gene-Disease Associations

genes associated with the increased adipose tissue around the neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased lung tissue damping Gene Set

From MPO Gene-Phenotype Associations

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

increased white adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased white adipose tissue 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.

increased brown adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased brown adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased subcutaneous adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased subcutaneous adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Plasminogen deficiency, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Plasminogen deficiency, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Plasminogen Deficiency, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Plasminogen Deficiency, Type I from the curated CTD Gene-Disease Associations dataset.

plasminogen Gene Set

From GeneRIF Biological Term Annotations

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

plasminogenplasmin Gene Set

From GeneRIF Biological Term Annotations

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

plasminogenbinding Gene Set

From GeneRIF Biological Term Annotations

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

plasminogenactivating Gene Set

From GeneRIF Biological Term Annotations

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

plasminogendependent Gene Set

From GeneRIF Biological Term Annotations

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

plasminogenmediated Gene Set

From GeneRIF Biological Term Annotations

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

positive regulation of plasminogen activation Gene Set

From GO Biological Process Annotations

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

regulation of plasminogen activation Gene Set

From GO Biological Process Annotations

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

plasminogen activation Gene Set

From GO Biological Process Annotations

genes participating in the plasminogen activation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of plasminogen activation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of plasminogen activation biological process from the curated GO Biological Process Annotations dataset.

Plasminogen-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasminogen-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

plasminogen deficiency, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the plasminogen deficiency, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

Plasminogen activating cascade Gene Set

From PANTHER Pathways

proteins participating in the Plasminogen activating cascade pathway from the PANTHER Pathways dataset.

increased concentration of hdl-c and decreased promoter activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased concentration of hdl-c and decreased promoter activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Sphingolipid activator protein 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sphingolipid activator protein 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ada2/gcn5/ada3 transcription activator complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ada2/gcn5/ada3 transcription activator complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

proteasome activator complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the proteasome activator complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

ada2/gcn5/ada3 transcription activator complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ada2/gcn5/ada3 transcription activator complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

nucleosomal methylation activator complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nucleosomal methylation activator complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

proteasome activator complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

RFC complex (activator A 1 complex) Gene Set

From CORUM Protein Complexes

proteins in the RFC complex (activator A 1 complex) protein complex from the CORUM Protein Complexes dataset.

NUMAC complex (nucleosomal methylation activator complex) Gene Set

From CORUM Protein Complexes

proteins in the NUMAC complex (nucleosomal methylation activator complex) protein complex from the CORUM Protein Complexes dataset.

activator Gene Set

From GeneRIF Biological Term Annotations

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

ada2/gcn5/ada3 transcription activator complex Gene Set

From GO Cellular Component Annotations

proteins localized to the ada2/gcn5/ada3 transcription activator complex cellular component from the curated GO Cellular Component Annotations dataset.

proteasome activator complex Gene Set

From GO Cellular Component Annotations

proteins localized to the proteasome activator complex cellular component from the curated GO Cellular Component Annotations dataset.

translation activator activity Gene Set

From GO Molecular Function Annotations

genes performing the translation activator activity molecular function from the curated GO Molecular Function Annotations dataset.

phospholipase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the phospholipase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

cysteine-type endopeptidase activator activity involved in apoptotic process Gene Set

From GO Molecular Function Annotations

genes performing the cysteine-type endopeptidase activator activity involved in apoptotic process molecular function from the curated GO Molecular Function Annotations dataset.

steroid receptor rna activator rna binding Gene Set

From GO Molecular Function Annotations

genes performing the steroid receptor rna activator rna binding molecular function from the curated GO Molecular Function Annotations dataset.

sphingomyelin phosphodiesterase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the sphingomyelin phosphodiesterase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

l-dopa decarboxylase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the l-dopa decarboxylase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

cyclin-dependent protein kinase 5 activator activity Gene Set

From GO Molecular Function Annotations

genes performing the cyclin-dependent protein kinase 5 activator activity molecular function from the curated GO Molecular Function Annotations dataset.

protein phosphatase type 1 activator activity Gene Set

From GO Molecular Function Annotations

genes performing the protein phosphatase type 1 activator activity molecular function from the curated GO Molecular Function Annotations dataset.

tyrosine 3-monooxygenase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the tyrosine 3-monooxygenase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

acetyltransferase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the acetyltransferase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

metalloenzyme activator activity Gene Set

From GO Molecular Function Annotations

genes performing the metalloenzyme activator activity molecular function from the curated GO Molecular Function Annotations dataset.

gtpase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the gtpase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

protein serine/threonine kinase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the protein serine/threonine kinase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

vitamin d receptor activator activity Gene Set

From GO Molecular Function Annotations

genes performing the vitamin d receptor activator activity molecular function from the curated GO Molecular Function Annotations dataset.

enzyme activator activity Gene Set

From GO Molecular Function Annotations

genes performing the enzyme activator activity molecular function from the curated GO Molecular Function Annotations dataset.

ornithine decarboxylase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the ornithine decarboxylase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

phosphatidylcholine-sterol o-acyltransferase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the phosphatidylcholine-sterol o-acyltransferase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

lipoprotein lipase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the lipoprotein lipase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

cyclase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the cyclase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

peptidase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the peptidase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

acetylcholine receptor activator activity Gene Set

From GO Molecular Function Annotations

genes performing the acetylcholine receptor activator activity molecular function from the curated GO Molecular Function Annotations dataset.

phosphatase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the phosphatase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

guanylate cyclase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the guanylate cyclase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

protein kinase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the protein kinase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

phospholipase a2 activator activity Gene Set

From GO Molecular Function Annotations

genes performing the phospholipase a2 activator activity molecular function from the curated GO Molecular Function Annotations dataset.

endopeptidase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the endopeptidase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

calcium sensitive guanylate cyclase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium sensitive guanylate cyclase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

protein tyrosine phosphatase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the protein tyrosine phosphatase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

deubiquitinase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the deubiquitinase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

receptor signaling protein tyrosine kinase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the receptor signaling protein tyrosine kinase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

peptidase activator activity involved in apoptotic process Gene Set

From GO Molecular Function Annotations

genes performing the peptidase activator activity involved in apoptotic process molecular function from the curated GO Molecular Function Annotations dataset.

protein phosphatase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the protein phosphatase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

superoxide-generating nadph oxidase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the superoxide-generating nadph oxidase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

kinase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the kinase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

atpase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the atpase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

protein tyrosine kinase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the protein tyrosine kinase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

transmembrane receptor protein tyrosine kinase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the transmembrane receptor protein tyrosine kinase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

thyroid hormone receptor activator activity Gene Set

From GO Molecular Function Annotations

genes performing the thyroid hormone receptor activator activity molecular function from the curated GO Molecular Function Annotations dataset.

receptor activator activity Gene Set

From GO Molecular Function Annotations

genes performing the receptor activator activity molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-protein transferase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-protein transferase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

lipase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the lipase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

neuropeptide head activator Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the neuropeptide head activator ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Proteasome component ECM29/Translational activator GCN1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proteasome component ECM29/Translational activator GCN1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Activator of Hsp90 ATPase homologue 1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Activator of Hsp90 ATPase homologue 1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription activator, Churchill Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription activator, Churchill protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcriptional activator NFYC/HAP5 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcriptional activator NFYC/HAP5 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cyclin-dependent kinase 5 activator Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cyclin-dependent kinase 5 activator protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Calcium-dependent secretion activator Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Calcium-dependent secretion activator protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcriptional activator, Zfx / Zfy domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcriptional activator, Zfx / Zfy domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

GATA-type transcription activator, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GATA-type transcription activator, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Signal transducer and activator of transcription 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Signal transducer and activator of transcription 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Disheveled-associated activator of morphogenesis 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Disheveled-associated activator of morphogenesis 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ganglioside GM2 activator Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ganglioside GM2 activator protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcriptional activator, plants Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcriptional activator, plants protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nuclear/hormone receptor activator site AF-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nuclear/hormone receptor activator site AF-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Activator of apoptosis harakiri Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Activator of apoptosis harakiri protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phosphotyrosyl phosphatase activator, PTPA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phosphotyrosyl phosphatase activator, PTPA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proteasome activator pa28, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proteasome activator pa28, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Steroid receptor RNA activator-protein/coat protein complex II, Sec31 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Steroid receptor RNA activator-protein/coat protein complex II, Sec31 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proteasome activator pa28, N-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proteasome activator pa28, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial ubiquitin ligase activator of NFKB 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial ubiquitin ligase activator of NFKB 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proteasome activator pa28 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proteasome activator pa28 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Coagulation factor XIIa/hepatocyte growth factor activator Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Coagulation factor XIIa/hepatocyte growth factor activator protein domain from the InterPro Predicted Protein Domain Annotations dataset.

D-amino acid oxidase activator Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the D-amino acid oxidase activator protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Activator of Hsp90 ATPase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Activator of Hsp90 ATPase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased fatty acid binding increased fat oxidation and insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased fatty acid binding increased fat oxidation and insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis, familial; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; amyloidosis, familial; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple familial trichoepithelioma and familial cylindromatosis Gene Set

From GAD Gene-Disease Associations

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

amyloidosis, familial; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis, familial; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hemiplegic migraine and benign familial infantile convulsions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

post-mrna release spliceosomal complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the post-mrna release spliceosomal complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

u2-type post-mrna release spliceosomal complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the u2-type post-mrna release spliceosomal complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

translation release factor complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the translation release factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

insulin release and insulin sensitivity Gene Set

From GAD Gene-Disease Associations

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

cytokine release Gene Set

From GAD Gene-Disease Associations

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

vascular t-pa release Gene Set

From GAD Gene-Disease Associations

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

interleukin 8 release after cardiac surgery Gene Set

From GAD Gene-Disease Associations

genes associated with the disease interleukin 8 release after cardiac surgery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

immunoglobulin e receptor-mediated histamine release from basophils Gene Set

From GAD Gene-Disease Associations

genes associated with the disease immunoglobulin e receptor-mediated histamine release from basophils in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

release Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of release of cytochrome c from mitochondria Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations dataset.

positive regulation of ryanodine-sensitive calcium-release channel activity by adrenergic receptor signaling pathway involved in positive regulation of cardiac muscle contraction Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of ryanodine-sensitive calcium-release channel activity by adrenergic receptor signaling pathway involved in positive regulation of cardiac muscle contraction biological process from the curated GO Biological Process Annotations dataset.

negative regulation of release of sequestered calcium ion into cytosol Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of release of sequestered calcium ion into cytosol biological process from the curated GO Biological Process Annotations dataset.

negative regulation of ryanodine-sensitive calcium-release channel activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of ryanodine-sensitive calcium-release channel activity biological process from the curated GO Biological Process Annotations dataset.

release of cytochrome c from mitochondria Gene Set

From GO Biological Process Annotations

genes participating in the release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations dataset.

release of sequestered calcium ion into cytosol Gene Set

From GO Biological Process Annotations

genes participating in the release of sequestered calcium ion into cytosol biological process from the curated GO Biological Process Annotations dataset.

release of cytoplasmic sequestered nf-kappab Gene Set

From GO Biological Process Annotations

genes participating in the release of cytoplasmic sequestered nf-kappab biological process from the curated GO Biological Process Annotations dataset.

viral release from host cell Gene Set

From GO Biological Process Annotations

genes participating in the viral release from host cell biological process from the curated GO Biological Process Annotations dataset.

positive regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion biological process from the curated GO Biological Process Annotations dataset.

regulation of release of sequestered calcium ion into cytosol Gene Set

From GO Biological Process Annotations

genes participating in the regulation of release of sequestered calcium ion into cytosol biological process from the curated GO Biological Process Annotations dataset.

release of sequestered calcium ion into cytosol by sarcoplasmic reticulum Gene Set

From GO Biological Process Annotations

genes participating in the release of sequestered calcium ion into cytosol by sarcoplasmic reticulum biological process from the curated GO Biological Process Annotations dataset.

positive regulation of release of cytochrome c from mitochondria Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations dataset.

positive regulation of ryanodine-sensitive calcium-release channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of ryanodine-sensitive calcium-release channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion Gene Set

From GO Biological Process Annotations

genes participating in the regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion biological process from the curated GO Biological Process Annotations dataset.

regulation of viral release from host cell Gene Set

From GO Biological Process Annotations

genes participating in the regulation of viral release from host cell biological process from the curated GO Biological Process Annotations dataset.

positive regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of ryanodine-sensitive calcium-release channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of ryanodine-sensitive calcium-release channel activity biological process from the curated GO Biological Process Annotations dataset.

release of matrix enzymes from mitochondria Gene Set

From GO Biological Process Annotations

genes participating in the release of matrix enzymes from mitochondria biological process from the curated GO Biological Process Annotations dataset.

gpi anchor release Gene Set

From GO Biological Process Annotations

genes participating in the gpi anchor release biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion biological process from the curated GO Biological Process Annotations dataset.

signal release Gene Set

From GO Biological Process Annotations

genes participating in the signal release biological process from the curated GO Biological Process Annotations dataset.

positive regulation of release of sequestered calcium ion into cytosol Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of release of sequestered calcium ion into cytosol biological process from the curated GO Biological Process Annotations dataset.

protein import into peroxisome matrix, substrate release Gene Set

From GO Biological Process Annotations

genes participating in the protein import into peroxisome matrix, substrate release biological process from the curated GO Biological Process Annotations dataset.

regulation of release of cytochrome c from mitochondria Gene Set

From GO Biological Process Annotations

genes participating in the regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations dataset.

positive regulation by host of viral release from host cell Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation by host of viral release from host cell biological process from the curated GO Biological Process Annotations dataset.

regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity biological process from the curated GO Biological Process Annotations dataset.

release from viral latency Gene Set

From GO Biological Process Annotations

genes participating in the release from viral latency biological process from the curated GO Biological Process Annotations dataset.

positive regulation of viral release from host cell Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of viral release from host cell biological process from the curated GO Biological Process Annotations dataset.

modulation by host of viral release from host cell Gene Set

From GO Biological Process Annotations

genes participating in the modulation by host of viral release from host cell biological process from the curated GO Biological Process Annotations dataset.

negative regulation of viral release from host cell Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of viral release from host cell biological process from the curated GO Biological Process Annotations dataset.

regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum Gene Set

From GO Biological Process Annotations

genes participating in the regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum biological process from the curated GO Biological Process Annotations dataset.

post-mrna release spliceosomal complex Gene Set

From GO Cellular Component Annotations

proteins localized to the post-mrna release spliceosomal complex cellular component from the curated GO Cellular Component Annotations dataset.

translation release factor complex Gene Set

From GO Cellular Component Annotations

proteins localized to the translation release factor complex cellular component from the curated GO Cellular Component Annotations dataset.

u2-type post-mrna release spliceosomal complex Gene Set

From GO Cellular Component Annotations

proteins localized to the u2-type post-mrna release spliceosomal complex cellular component from the curated GO Cellular Component Annotations dataset.

inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity Gene Set

From GO Molecular Function Annotations

genes performing the inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity molecular function from the curated GO Molecular Function Annotations dataset.

ryanodine-sensitive calcium-release channel activity Gene Set

From GO Molecular Function Annotations

genes performing the ryanodine-sensitive calcium-release channel activity molecular function from the curated GO Molecular Function Annotations dataset.

calcium-induced calcium release activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium-induced calcium release activity molecular function from the curated GO Molecular Function Annotations dataset.

translation release factor activity Gene Set

From GO Molecular Function Annotations

genes performing the translation release factor activity molecular function from the curated GO Molecular Function Annotations dataset.

translation release factor activity, codon specific Gene Set

From GO Molecular Function Annotations

genes performing the translation release factor activity, codon specific molecular function from the curated GO Molecular Function Annotations dataset.

translation release factor activity, codon nonspecific Gene Set

From GO Molecular Function Annotations

genes performing the translation release factor activity, codon nonspecific molecular function from the curated GO Molecular Function Annotations dataset.

naadp-sensitive calcium-release channel activity Gene Set

From GO Molecular Function Annotations

genes performing the naadp-sensitive calcium-release channel activity molecular function from the curated GO Molecular Function Annotations dataset.

calcium-release channel activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium-release channel activity molecular function from the curated GO Molecular Function Annotations dataset.

frontal release signs Gene Set

From HPO Gene-Disease Associations

genes associated with the frontal release signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Peptide chain release factor class I/class II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptide chain release factor class I/class II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptide chain release factor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptide chain release factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Calcium release-activated calcium channel protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Calcium release-activated calcium channel protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptide Chain Release Factor eRF1/aRF1, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptide Chain Release Factor eRF1/aRF1, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Translation release factor pelota Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Translation release factor pelota protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-(glutamine-N5) methyltransferase, release factor-specific Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-(glutamine-N5) methyltransferase, release factor-specific protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptide chain release factor eRF1/aRF1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptide chain release factor eRF1/aRF1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal synaptic norepinephrine release Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal synaptic norepinephrine release phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal synaptic dopamine release Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal synaptic dopamine release phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal synaptic acetylcholine release Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal synaptic acetylcholine release phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal synaptic glutamate release Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal synaptic glutamate release phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Enkephalin release Gene Set

From PANTHER Pathways

proteins participating in the Enkephalin release pathway from the PANTHER Pathways dataset.

Acetylcholine Neurotransmitter Release Cycle Gene Set

From Reactome Pathways

proteins participating in the Acetylcholine Neurotransmitter Release Cycle pathway from the Reactome Pathways dataset.

Erythrocytes take up carbon dioxide and release oxygen Gene Set

From Reactome Pathways

proteins participating in the Erythrocytes take up carbon dioxide and release oxygen pathway from the Reactome Pathways dataset.

Serotonin Neurotransmitter Release Cycle Gene Set

From Reactome Pathways

proteins participating in the Serotonin Neurotransmitter Release Cycle pathway from the Reactome Pathways dataset.

Release of apoptotic factors from the mitochondria Gene Set

From Reactome Pathways

proteins participating in the Release of apoptotic factors from the mitochondria pathway from the Reactome Pathways dataset.

Glutamate Neurotransmitter Release Cycle Gene Set

From Reactome Pathways

proteins participating in the Glutamate Neurotransmitter Release Cycle pathway from the Reactome Pathways dataset.

Erythrocytes take up oxygen and release carbon dioxide Gene Set

From Reactome Pathways

proteins participating in the Erythrocytes take up oxygen and release carbon dioxide pathway from the Reactome Pathways dataset.

Release of eIF4E Gene Set

From Reactome Pathways

proteins participating in the Release of eIF4E pathway from the Reactome Pathways dataset.

Neurotransmitter Release Cycle Gene Set

From Reactome Pathways

proteins participating in the Neurotransmitter Release Cycle pathway from the Reactome Pathways dataset.

Norepinephrine Neurotransmitter Release Cycle Gene Set

From Reactome Pathways

proteins participating in the Norepinephrine Neurotransmitter Release Cycle pathway from the Reactome Pathways dataset.

Dopamine Neurotransmitter Release Cycle Gene Set

From Reactome Pathways

proteins participating in the Dopamine Neurotransmitter Release Cycle pathway from the Reactome Pathways dataset.

GABA synthesis, release, reuptake and degradation Gene Set

From Reactome Pathways

proteins participating in the GABA synthesis, release, reuptake and degradation pathway from the Reactome Pathways dataset.

Release of Hh-Np from the secreting cell Gene Set

From Reactome Pathways

proteins participating in the Release of Hh-Np from the secreting cell pathway from the Reactome Pathways dataset.

Virus Assembly and Release Gene Set

From Reactome Pathways

proteins participating in the Virus Assembly and Release pathway from the Reactome Pathways dataset.

Neurotransmitter Release Cycle(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Neurotransmitter Release Cycle(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Thrombophilia, histidine-rich glycoprotein-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, histidine-rich glycoprotein-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia from the curated CTD Gene-Disease Associations dataset.

Thrombophilia, hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia, hereditary from the curated CTD Gene-Disease Associations dataset.

thrombophilia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

thrombophilia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease thrombophilia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

thrombophilia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ahg deficiency disease; hemophilia a; hemorrhage; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hemorrhage; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood platelet disorders; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood platelet disorders; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

femur head necrosis; hyperhomocysteinemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease femur head necrosis; hyperhomocysteinemia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; hyperhomocysteinemia; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; hyperhomocysteinemia; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; thromboembolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mesenteric vascular occlusion; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mesenteric vascular occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; thrombophilia; thrombosis; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; thrombophilia; thrombosis; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intracranial thrombosis; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombophilia Gene Set

From GAD Gene-Disease Associations

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

recurrence; thrombophilia; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

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

colonic polyps; gastrointestinal diseases; inflammatory bowel disease, nos; inflammatory bowel diseases; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colonic polyps; gastrointestinal diseases; inflammatory bowel disease, nos; inflammatory bowel diseases; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

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

hyperhomocysteinemia; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal growth retardation; pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal growth retardation; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemophilia a; hemophilia b; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemophilia a; hemophilia b; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; thromboembolism; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; thromboembolism; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; osteonecrosis; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; osteonecrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; abortion, spontaneous; obstetric labor complications; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; abortion, spontaneous; obstetric labor complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

protein s deficiency; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced; pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deep vein thrombophilia Gene Set

From GAD Gene-Disease Associations

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

activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; infertility; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; infertility; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboangiitis obliterans; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

renal insufficiency; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

hyperhomocysteinemia; recurrence; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; recurrence; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; osteonecrosis; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; osteonecrosis; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

blood coagulation disorders, inherited; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; pregnancy complications; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; pregnancy complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; abruptio placentae; activated protein c resistance; placenta abruptio; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; abruptio placentae; activated protein c resistance; placenta abruptio; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

activated protein c resistance; homocystinuria; hyperhomocysteinemia; muscle spasticity; sepsis; septic shock; shock, septic; systemic infection; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; homocystinuria; hyperhomocysteinemia; muscle spasticity; sepsis; septic shock; shock, septic; systemic infection; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombophilia; thrombosis; venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

antiphospholipid syndrome; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombophilia; thrombosis; varicose veins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thrombophilia; thrombosis; varicose veins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gaucher disease; legg-perthes disease; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gaucher disease; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloproliferative disorders; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

intracranial embolism; migraine disorders; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intracranial embolism; migraine disorders; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhage; placenta diseases; premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhage; placenta diseases; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; cardiovascular diseases; polycythemia vera; recurrence; thrombocythemia, hemorrhagic; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; cardiovascular diseases; polycythemia vera; recurrence; thrombocythemia, hemorrhagic; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; intracranial thrombosis; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; intracranial thrombosis; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; hyperhomocysteinemia; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; hyperhomocysteinemia; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coagulation protein disorders; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coagulation protein disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; activated protein c resistance; infertility, female; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; activated protein c resistance; infertility, female; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; hematologic neoplasms; precursor cell lymphoblastic leukemia-lymphoma; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; hematologic neoplasms; precursor cell lymphoblastic leukemia-lymphoma; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombophilia; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

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

activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; peripheral vascular diseases; recurrence; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; peripheral vascular diseases; recurrence; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sinus thrombosis, intracranial; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sinus thrombosis, intracranial; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, hematologic; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications, hematologic; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, hematologic; premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications, hematologic; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

budd-chiari syndrome; hyperhomocysteinemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease budd-chiari syndrome; hyperhomocysteinemia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colitis, ulcerative; hyperhomocysteinemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis, ulcerative; hyperhomocysteinemia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal loss ; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

epilepsy; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis; wegener granulomatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis; wegener granulomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; legg-perthes disease; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein occlusion; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; hyperhomocysteinemia; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; hyperhomocysteinemia; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; infection; neoplasms; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; infection; neoplasms; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhage; recurrence; thromboembolism; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhage; recurrence; thromboembolism; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

placenta diseases; pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease placenta diseases; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms; recurrence; thromboembolism; thrombophilia; upper extremity deep vein thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms; recurrence; thromboembolism; thrombophilia; upper extremity deep vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary thrombophilia. Gene Set

From GAD Gene-Disease Associations

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

embryo loss; habitual aborter nos; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease embryo loss; habitual aborter nos; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abortion, spontaneous; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

activated protein c resistance; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrence; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrence; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; myocardial infarction; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; myocardial infarction; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

factor v deficiency; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease factor v deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta-thalassemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abruptio placentae; placenta abruptio; pregnancy complications; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; placenta abruptio; pregnancy complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

liver cirrhosis; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease liver cirrhosis; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

precursor cell lymphoblastic leukemia-lymphoma; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease precursor cell lymphoblastic leukemia-lymphoma; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrence; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

arteriosclerosis; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

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

gaucher disease; hypertension, pulmonary; necrosis; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gaucher disease; hypertension, pulmonary; necrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombocythemia, essential; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thrombocythemia, essential; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hellp syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abortion, spontaneous; abruptio placentae; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombophilia; varicose ulcer; varicose veins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thrombophilia; varicose ulcer; varicose veins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; placenta abruptio; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; placenta abruptio; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteonecrosis; thrombophilia; hypofibrinolysis Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

venous thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; thromboembolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; hemochromatosis; iron overload; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; hemochromatosis; iron overload; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

budd-chiari syndrome; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease budd-chiari syndrome; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

constriction, pathologic; ischemia; peripheral arterial disease; peripheral arterial diseases; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; ischemia; peripheral arterial disease; peripheral arterial diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhage; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abnormal fibrin polymerization and thrombophilia Gene Set

From GAD Gene-Disease Associations

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

henoch-schoenlein purpura; purpura, schoenlein-henoch; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease henoch-schoenlein purpura; purpura, schoenlein-henoch; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stomach neoplasms; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

thrombophilia Gene Set

From GeneRIF Biological Term Annotations

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

thrombophilia Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease thrombophilia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Thrombophilia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Thrombophilia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Carbonic anhydrase va deficiency, hyperammonemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SCID due to ADA deficiency, delayed onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency due to ADA deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

HNSHA due to aldolase A deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease, atypical, due to saposin C deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to inborn errors of metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia due to hexokinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocysteinemia due to MTHFR deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to ficolin 3 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermethioninemia due to adenosine kinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to defect in cd3-zeta Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria due to MTHFR deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex II deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, severe, due to leptin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenylate kinase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.

Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.

Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Congenital thrombotic disease, due to Protein C deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.

ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset.

Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To 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.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

Severe combined immunodeficiency due to adenosine deaminase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe combined immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset.

Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency from the curated CTD Gene-Disease Associations dataset.

Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset.

Krabbe Disease, Atypical, due to Saposin A Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset.

HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset.

Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset.

Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in CD3-Zeta Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset.

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Metachromatic Leukodystrophy due to Saposin B Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metachromatic Leukodystrophy due to Saposin B Deficiency from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.

thrombocytopenia due to platelet alloimmunization Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease thrombocytopenia due to platelet alloimmunization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pneumoconiosis due to talc Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease pneumoconiosis due to talc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

hereditary spastic paraparesis due to a frame shift mutat Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

depressed suicide; suicide due to depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depressed suicide; suicide due to depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

due Gene Set

From GeneRIF Biological Term Annotations

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

anemia due to reduced life span of red cells Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the anemia due to reduced life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

anemia due to reduced life span of red cells Gene Set

From HPO Gene-Disease Associations

genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restricted neck movement due to contractures Gene Set

From HPO Gene-Disease Associations

genes associated with the restricted neck movement due to contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic rhinitis due to narrow nasal airway Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic rhinitis due to narrow nasal airway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bowing of limbs due to multiple fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory insufficiency due to muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis leading to amputation due to slow healing fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis leading to amputation due to slow healing fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

weakness due to upper motor neuron dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

self-mutilation of tongue and lips due to involuntary movements Gene Set

From HPO Gene-Disease Associations

genes associated with the self-mutilation of tongue and lips due to involuntary movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory insufficiency due to defective ciliary clearance Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency due to defective ciliary clearance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent infections due to aspiration Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent infections due to aspiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypotonia due to defect at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic hepatitis due to cryptospridium infection Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic hepatitis due to cryptospridium infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

subperiosteal erosions due to secondary hyperparathyroidism Gene Set

From HPO Gene-Disease Associations

genes associated with the subperiosteal erosions due to secondary hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

painless fractures due to injury Gene Set

From HPO Gene-Disease Associations

genes associated with the painless fractures due to injury phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic abscesses due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the hepatic abscesses due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cellulitis due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the cellulitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intermittent episodes of respiratory insufficiency due to muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the intermittent episodes of respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

orthostatic hypotension due to autonomic dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the orthostatic hypotension due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

{chronic infections, due to mbl deficiency} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {chronic infections, due to mbl deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency due to il2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency due to il2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder due to p2rx1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to phosphofructokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to phosphofructokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

nephropathy due to cfhr5 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephropathy due to cfhr5 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset.

megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease, autosomal, due to deficiency of cyba Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease, autosomal, due to deficiency of cyba phenotype from the curated OMIM Gene-Disease Associations dataset.

?isolated growth hormone deficiency due to defect in ghrf Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, morbid, due to leptin receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, morbid, due to leptin receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypercholesterolemia, due to ligand-defective apo b Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypercholesterolemia, due to ligand-defective apo b phenotype from the curated OMIM Gene-Disease Associations dataset.

glucocorticoid deficiency, due to acth unresponsiveness Gene Set

From OMIM Gene-Disease Associations

genes associated with the glucocorticoid deficiency, due to acth unresponsiveness phenotype from the curated OMIM Gene-Disease Associations dataset.

disordered steroidogenesis due to cytochrome p450 oxidoreductase Gene Set

From OMIM Gene-Disease Associations

genes associated with the disordered steroidogenesis due to cytochrome p450 oxidoreductase phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemorrhagic diathesis due to 'antithrombin' pittsburgh Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemorrhagic diathesis due to 'antithrombin' pittsburgh phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to purine nucleoside phosphorylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to purine nucleoside phosphorylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione peroxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione peroxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

lacticacidemia due to pdx1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the lacticacidemia due to pdx1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

omphalocele due to duplication of 1p31.3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the omphalocele due to duplication of 1p31.3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to itga7 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, hemolytic, due to umph1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, hemolytic, due to umph1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

homocystinuria due to mthfr deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocystinuria due to mthfr deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency due to ada deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency due to ada deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial complex i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

cirrhosis due to liver phosphorylase kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the cirrhosis due to liver phosphorylase kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

metachromatic leukodystrophy due to sap-b deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the metachromatic leukodystrophy due to sap-b deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

gigantism due to ghrf hypersecretion Gene Set

From OMIM Gene-Disease Associations

genes associated with the gigantism due to ghrf hypersecretion phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, morbid, due to leptin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, morbid, due to leptin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome, due to cox deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome, due to cox deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

macrocytic anemia, refractory, due to 5q deletion, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocytic anemia, refractory, due to 5q deletion, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

growth retardation with deafness and mental retardation due to igf1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation with deafness and mental retardation due to igf1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperammonemia due to carbonic anhydrase va deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperammonemia due to carbonic anhydrase va deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to g6pd deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to g6pd deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{drug-induced liver injury due to flucloxacillin} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {drug-induced liver injury due to flucloxacillin} phenotype from the curated OMIM Gene-Disease Associations dataset.

?male pseudohermaphroditism due to defective lh Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male pseudohermaphroditism due to defective lh phenotype from the curated OMIM Gene-Disease Associations dataset.

hydrocephalus due to aqueductal stenosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the hydrocephalus due to aqueductal stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type i, due to tap2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type i, due to tap2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to adenylate kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to adenylate kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

emphysema due to aat deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the emphysema due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

erythrocytosis due to bisphosphoglycerate mutase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the erythrocytosis due to bisphosphoglycerate mutase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thalassemia due to hb lepore Gene Set

From OMIM Gene-Disease Associations

genes associated with the thalassemia due to hb lepore phenotype from the curated OMIM Gene-Disease Associations dataset.

rickets due to defect in vitamin d 25-hydroxylation Gene Set

From OMIM Gene-Disease Associations

genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset.

aica-ribosiduria due to atic deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the aica-ribosiduria due to atic deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoaldosteronism, congenital, due to cmo i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoaldosteronism, congenital, due to cmo i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial cox4 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial cox4 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria due to transcobalamin receptor defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria due to transcobalamin receptor defect phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease due to deficiency of ncf-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease due to deficiency of ncf-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease due to deficiency of ncf-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease due to deficiency of ncf-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia due to adenosine kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia due to adenosine kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, due to sepiapterin reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, due to sepiapterin reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to defect in mapbp-interacting protein Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to cytochrome c oxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to cytochrome c oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

pyogenic bacterial infections, recurrent, due to myd88 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyogenic bacterial infections, recurrent, due to myd88 deficiency 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.

immunodeficiency due to ficolin 3 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to ficolin 3 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial complex 1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial complex 1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to triosephosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to triosephosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{resistance to malaria due to g6pd deficiency} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {resistance to malaria due to g6pd deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to hexokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to hexokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemosiderosis, systemic, due to aceruloplasminemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemosiderosis, systemic, due to aceruloplasminemia phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy due to cpt ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy due to cpt ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

emphysema-cirrhosis, due to aat deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the emphysema-cirrhosis, due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoaldosteronism, congenital, due to cmo ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoaldosteronism, congenital, due to cmo ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

?male infertility due to acrosin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male infertility due to acrosin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy due to myoadenylate deaminase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy due to myoadenylate deaminase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Gene Set

From Reactome Pathways

proteins participating in the Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) pathway from the Reactome Pathways dataset.

Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) pathway from the Wikipathways 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.

fibronectin-tissue transglutaminase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the fibronectin-tissue transglutaminase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

connective tissue-activating peptide Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical connective tissue-activating peptide from the curated CTD Gene-Chemical Interactions dataset.

Soft Tissue Neoplasms Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Soft Tissue Neoplasms from the curated CTD Gene-Disease Associations dataset.

Neoplasms, Bone Tissue Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neoplasms, Bone Tissue from the curated CTD Gene-Disease Associations dataset.

Connective Tissue Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Connective Tissue Diseases from the curated CTD Gene-Disease Associations dataset.

teeth hard tissue disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease teeth hard tissue disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

muscle tissue disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease muscle tissue disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

connective tissue disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease connective tissue disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

connective tissue cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease connective tissue cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

teeth hard tissue disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease teeth hard tissue disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

connective tissue disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease connective tissue disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

connective tissue cancer Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease connective tissue cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

muscle tissue disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease muscle tissue disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

connective tissue cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease connective tissue cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

teeth hard tissue disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease teeth hard tissue disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mixed connective tissue disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mixed connective tissue disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

autoimmune disease of skin and connective tissue Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autoimmune disease of skin and connective tissue in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

connective tissue benign neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscle tissue disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

connective tissue disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

mucosa-associated lymphoid tissue lymphoma Gene Set

From GAD Gene-Disease Associations

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

connective tissue diseases; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease connective tissue diseases; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

connective tissue dysplasias Gene Set

From GAD Gene-Disease Associations

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

adipose-tissue tumors Gene Set

From GAD Gene-Disease Associations

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

adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

granuloma; mixed connective tissue disease; sarcoidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease granuloma; mixed connective tissue disease; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone cancer; soft tissue sarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone cancer; soft tissue sarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high-grade soft tissue sarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high-grade soft tissue sarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

connective tissue diseases; ectopia lentis; marfan syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease connective tissue diseases; ectopia lentis; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

shoulder dislocation; soft tissue injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease shoulder dislocation; soft tissue injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

soft tissue sarcoma Gene Set

From GAD Gene-Disease Associations

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

connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; mixed connective tissue disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; mixed connective tissue disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malignant cystosarcoma phyllodes and soft tissue sarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malignant cystosarcoma phyllodes and soft tissue sarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cyp1a1 levels in lung tissue Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cyp1a1 levels in lung tissue in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphomas of mucosa-associated lymphoid tissue. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphomas of mucosa-associated lymphoid tissue. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adhesions; peritoneal diseases; tissue adhesions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adhesions; peritoneal diseases; tissue adhesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, b-cell, marginal zone; mucosa-associated lymphoid tissue lymphoma; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, b-cell, marginal zone; mucosa-associated lymphoid tissue lymphoma; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrosarcoma; myxoma; soft tissue neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrosarcoma; myxoma; soft tissue neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tissue Gene Set

From GeneRIF Biological Term Annotations

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

SCA1_Knock-in_GDS1756_233_mouse_Forebrain tissue - 4 weeks of age Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the SCA1_Knock-in_GDS1756_233_mouse_Forebrain tissue - 4 weeks of age gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

SIRT3_KO_GDS4058_16_mouse_BROWN ADIPOSE TISSUE Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the SIRT3_KO_GDS4058_16_mouse_BROWN ADIPOSE TISSUE gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

KDM1A_KD_GDS5055_367_mouse_adipose tissue Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the KDM1A_KD_GDS5055_367_mouse_adipose tissue gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

FSP27_KO_GDS3768_514_mouse_White adipose tissue (WAT) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the FSP27_KO_GDS3768_514_mouse_White adipose tissue (WAT) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

SCA1_Knock-in_GDS1756_231_mouse_Cerebellum tissue - 4 weeks of age Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the SCA1_Knock-in_GDS1756_231_mouse_Cerebellum tissue - 4 weeks of age gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

CLDN18_KO_GDS4961_28_mouse_whole lung tissue Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the CLDN18_KO_GDS4961_28_mouse_whole lung tissue gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

SIRT3_KO_GDS4058_454_mouse_BROWN ADIPOSE TISSUE Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the SIRT3_KO_GDS4058_454_mouse_BROWN ADIPOSE TISSUE gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

SCA1_Knock-in_GDS1756_232_mouse_Cerebellum tissue - 12 weeks of age Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the SCA1_Knock-in_GDS1756_232_mouse_Cerebellum tissue - 12 weeks of age gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

SCA1_Knock-in_GDS1756_234_mouse_Forebrain tissue - 12 weeks of age Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the SCA1_Knock-in_GDS1756_234_mouse_Forebrain tissue - 12 weeks of age gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

TGFB2_KD_GDS4483_351_mouse_Embryonic palatal tissue Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the TGFB2_KD_GDS4483_351_mouse_Embryonic palatal tissue gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

GK_KO_GDS2610_162_mouse_Brown adipose tissue Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the GK_KO_GDS2610_162_mouse_Brown adipose tissue gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

Otx2_KO_GDS4440_143_mouse_fourth ventricular choroid plexus tissue Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the Otx2_KO_GDS4440_143_mouse_fourth ventricular choroid plexus tissue gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

PRDM16_DEPLETION_GDS4021_460_mouse_WAT - white adipose tissue (stromal-vascular cells) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the PRDM16_DEPLETION_GDS4021_460_mouse_WAT - white adipose tissue (stromal-vascular cells) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

KDM1A_KD_GDS5055_457_mouse_adipose tissue Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the KDM1A_KD_GDS5055_457_mouse_adipose tissue gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

PHGDH_KO_GDS2874_125_mouse_embryonic head tissue Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the PHGDH_KO_GDS2874_125_mouse_embryonic head tissue gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

SFRP5_KO_GDS4988_27_mouse_gonadal white adipose tissue HFD Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the SFRP5_KO_GDS4988_27_mouse_gonadal white adipose tissue HFD gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations

genes participating in the skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations dataset.

skeletal muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the skeletal muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of planar cell polarity pathway involved in cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of planar cell polarity pathway involved in cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cardiac muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cardiac muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

chemical homeostasis within a tissue Gene Set

From GO Biological Process Annotations

genes participating in the chemical homeostasis within a tissue biological process from the curated GO Biological Process Annotations dataset.

immunoglobulin production in mucosal tissue Gene Set

From GO Biological Process Annotations

genes participating in the immunoglobulin production in mucosal tissue biological process from the curated GO Biological Process Annotations dataset.

regulation of immunoglobulin production in mucosal tissue Gene Set

From GO Biological Process Annotations

genes participating in the regulation of immunoglobulin production in mucosal tissue biological process from the curated GO Biological Process Annotations dataset.

regulation of planar cell polarity pathway involved in cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of planar cell polarity pathway involved in cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations

genes participating in the skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations dataset.

tissue remodeling Gene Set

From GO Biological Process Annotations

genes participating in the tissue remodeling biological process from the curated GO Biological Process Annotations dataset.

negative regulation of biomineral tissue development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of biomineral tissue development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of tissue remodeling Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of tissue remodeling biological process from the curated GO Biological Process Annotations dataset.

connective tissue development Gene Set

From GO Biological Process Annotations

genes participating in the connective tissue development biological process from the curated GO Biological Process Annotations dataset.

regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations

genes participating in the regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

striated muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the striated muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of striated muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of striated muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

aorta smooth muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the aorta smooth muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

planar cell polarity pathway involved in cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the planar cell polarity pathway involved in cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

organ or tissue specific immune response Gene Set

From GO Biological Process Annotations

genes participating in the organ or tissue specific immune response biological process from the curated GO Biological Process Annotations dataset.

adipose tissue development Gene Set

From GO Biological Process Annotations

genes participating in the adipose tissue development biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle tissue regeneration Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle tissue regeneration biological process from the curated GO Biological Process Annotations dataset.

atrial cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the atrial cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations dataset.

tissue homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the tissue homeostasis biological process from the curated GO Biological Process Annotations dataset.

right ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the right ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of cell proliferation involved in tissue homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cell proliferation involved in tissue homeostasis biological process from the curated GO Biological Process Annotations dataset.

kidney smooth muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the kidney smooth muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations dataset.

regulation of connective tissue growth factor production Gene Set

From GO Biological Process Annotations

genes participating in the regulation of connective tissue growth factor production biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

connective tissue replacement involved in inflammatory response wound healing Gene Set

From GO Biological Process Annotations

genes participating in the connective tissue replacement involved in inflammatory response wound healing biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cardiac muscle tissue growth Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cardiac muscle tissue growth biological process from the curated GO Biological Process Annotations dataset.

regulation of muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

mucosal-associated lymphoid tissue development Gene Set

From GO Biological Process Annotations

genes participating in the mucosal-associated lymphoid tissue development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle tissue growth involved in heart morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle tissue growth involved in heart morphogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations dataset.

positive regulation of immunoglobulin production in mucosal tissue Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of immunoglobulin production in mucosal tissue biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle tissue growth Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle tissue growth biological process from the curated GO Biological Process Annotations dataset.

tissue development Gene Set

From GO Biological Process Annotations

genes participating in the tissue development biological process from the curated GO Biological Process Annotations dataset.

muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle tissue growth Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle tissue growth biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac muscle tissue growth Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac muscle tissue growth biological process from the curated GO Biological Process Annotations dataset.

secretion by tissue Gene Set

From GO Biological Process Annotations

genes participating in the secretion by tissue biological process from the curated GO Biological Process Annotations dataset.

positive regulation of biomineral tissue development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of biomineral tissue development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of tissue remodeling Gene Set

From GO Biological Process Annotations

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

left ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the left ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of striated muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of striated muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

homeostasis of number of cells within a tissue Gene Set

From GO Biological Process Annotations

genes participating in the homeostasis of number of cells within a tissue biological process from the curated GO Biological Process Annotations dataset.

connective tissue growth factor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the connective tissue growth factor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

regulation of tissue remodeling Gene Set

From GO Biological Process Annotations

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

biomineral tissue development Gene Set

From GO Biological Process Annotations

genes participating in the biomineral tissue development biological process from the curated GO Biological Process Annotations dataset.

regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

regulation of skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations

genes participating in the regulation of skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations dataset.

tissue migration Gene Set

From GO Biological Process Annotations

genes participating in the tissue migration biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

establishment of tissue polarity Gene Set

From GO Biological Process Annotations

genes participating in the establishment of tissue polarity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of connective tissue growth factor production Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of connective tissue growth factor production biological process from the curated GO Biological Process Annotations dataset.

metanephric smooth muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric smooth muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

antigen transcytosis by m cells in mucosal-associated lymphoid tissue Gene Set

From GO Biological Process Annotations

genes participating in the antigen transcytosis by m cells in mucosal-associated lymphoid tissue biological process from the curated GO Biological Process Annotations dataset.

regulation of biomineral tissue development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of biomineral tissue development biological process from the curated GO Biological Process Annotations dataset.

smooth muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the smooth muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

tissue regeneration Gene Set

From GO Biological Process Annotations

genes participating in the tissue regeneration biological process from the curated GO Biological Process Annotations dataset.

positive regulation of striated muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of striated muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

adipose tissue Gene Set

From GTEx Tissue Gene Expression Profiles

genes with high or low expression in adipose tissue relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.

Visceral adipose tissue adjusted for BMI Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Visceral adipose tissue adjusted for BMI phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Subcutaneous adipose tissue Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Subcutaneous adipose tissue phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

connective tissue cancer Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease connective tissue cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

teeth hard tissue disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease teeth hard tissue disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

connective tissue disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease connective tissue disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

muscle tissue disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease muscle tissue disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

abnormality of connective tissue Gene Set

From GWASdb SNP-Phenotype Associations

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

nervous tissue neoplasm Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the nervous tissue neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of adipose tissue Gene Set

From GWASdb SNP-Phenotype Associations

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

depletion of mitochondrial dna in muscle tissue Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the depletion of mitochondrial dna in muscle tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

adipose tissue Gene Set

From HPA Tissue Gene Expression Profiles

genes with high or low expression in adipose tissue relative to other tissues from the HPA Tissue Gene Expression Profiles dataset.

soft tissue Gene Set

From HPA Tissue Protein Expression Profiles

proteins with high or low expression in soft tissue relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.

fullness of paranasal tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the fullness of paranasal tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of connective tissue Gene Set

From HPO Gene-Disease Associations

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

abnormal mitochondria in muscle tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal mitochondria in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal subcutaneous fat tissue distribution Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal subcutaneous fat tissue distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of fatty tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of fatty tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reduced subcutaneous adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gonadal tissue inappropriate for external genitalia or chromosomal sex Gene Set

From HPO Gene-Disease Associations

genes associated with the gonadal tissue inappropriate for external genitalia or chromosomal sex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ectopic ossification in ligament tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the ectopic ossification in ligament tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of subcutaneous adipose tissue in limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of subcutaneous adipose tissue in limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lack of subcutaneous fatty tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the lack of subcutaneous fatty tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of truncal subcutaneous adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of truncal subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of facial soft tissue Gene Set

From HPO Gene-Disease Associations

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

nervous tissue neoplasm Gene Set

From HPO Gene-Disease Associations

genes associated with the nervous tissue neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ectopic ossification in muscle tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the ectopic ossification in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

connective tissue nevi Gene Set

From HPO Gene-Disease Associations

genes associated with the connective tissue nevi phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fibrous tissue neoplasm Gene Set

From HPO Gene-Disease Associations

genes associated with the fibrous tissue neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of adipose tissue Gene Set

From HPO Gene-Disease Associations

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

abnormality of facial adipose tissue Gene Set

From HPO Gene-Disease Associations

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

soft tissue swelling of interphalangeal joints Gene Set

From HPO Gene-Disease Associations

genes associated with the soft tissue swelling of interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ectopic ossification in tendon tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the ectopic ossification in tendon tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of subcutaneous fat tissue Gene Set

From HPO Gene-Disease Associations

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

yellow subcutaneous tissue covered by thin, scaly skin Gene Set

From HPO Gene-Disease Associations

genes associated with the yellow subcutaneous tissue covered by thin, scaly skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated tissue non-specific alkaline phosphatase Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated tissue non-specific alkaline phosphatase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of facial adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of facial adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of gluteal subcutaneous adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of gluteal subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic) Gene Set

From HPO Gene-Disease Associations

genes associated with the nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adipose tissue loss Gene Set

From HPO Gene-Disease Associations

genes associated with the adipose tissue loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

depletion of mitochondrial dna in muscle tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the depletion of mitochondrial dna in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Mixed Connective Tissue Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mixed Connective Tissue Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Soft Tissue Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Soft Tissue Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Neoplasms, Gonadal Tissue Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neoplasms, Gonadal Tissue phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Neoplasms, Nerve Tissue Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neoplasms, Nerve Tissue phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Lymphoma, Mucosa-Associated Lymphoid Tissue Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lymphoma, Mucosa-Associated Lymphoid Tissue phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Soft Tissue Injuries Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Soft Tissue Injuries phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Neoplasms, Bone Tissue Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neoplasms, Bone Tissue phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Connective Tissue Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Connective Tissue Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Tissue factor/coagulation factor III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tissue factor/coagulation factor III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proteinase inhibitor I35, tissue inhibitor of metalloproteinase, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proteinase inhibitor I35, tissue inhibitor of metalloproteinase, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tissue alpha-L-fucosidase Gene Set

From InterPro Predicted Protein Domain Annotations

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

Tissue inhibitor of metalloprotease 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tissue inhibitor of metalloprotease 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tissue inhibitor of metalloprotease 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tissue inhibitor of metalloprotease 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tissue inhibitor of metalloprotease 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tissue inhibitor of metalloprotease 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tissue factor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tissue factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proteinase inhibitor I35, tissue inhibitor of metalloproteinase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proteinase inhibitor I35, tissue inhibitor of metalloproteinase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tissue inhibitor of metalloproteinases-like, OB-fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tissue inhibitor of metalloproteinases-like, OB-fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tissue factor pathway inhibitor 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tissue factor pathway inhibitor 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tissue factor pathway inhibitor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tissue factor pathway inhibitor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

adipose tissue necrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the adipose tissue necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal embryonic tissue morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brown adipose tissue physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brown adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brown adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal adipose tissue physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal extraembryonic tissue morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brown adipose tissue thermogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brown adipose tissue thermogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal aorta elastic tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal aorta elastic tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal adipose tissue development Gene Set

From MPO Gene-Phenotype Associations

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

absent subcutaneous adipose tissue Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent subcutaneous adipose tissue phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brown adipose tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brown adipose tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tooth hard tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal tooth hard tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal extraembryonic tissue physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

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

embryo tissue necrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the embryo tissue necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal white adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mucosa-associated lymphoid tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mucosa-associated lymphoid tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

persistence of notochord tissue Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the persistence of notochord tissue phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mammary gland connective tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mammary gland connective tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel elastic tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel elastic tissue morphology 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.

abnormal gut-associated lymphoid tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal gut-associated lymphoid tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal adipose tissue distribution Gene Set

From MPO Gene-Phenotype Associations

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

disorganized embryonic tissue Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized embryonic tissue phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal testis interstitial tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal testis interstitial tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

adipose tissue phenotype Gene Set

From MPO Gene-Phenotype Associations

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

abnormal white adipose tissue physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal oropharyngeal lymphoid tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal oropharyngeal lymphoid tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal white adipose tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white adipose tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal adipose tissue morphology Gene Set

From MPO Gene-Phenotype Associations

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

aortic elastic tissue lesions Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aortic elastic tissue lesions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac muscle tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac muscle tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized extraembryonic tissue Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized extraembryonic tissue phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal embryonic tissue physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal lung tissue damping Gene Set

From MPO Gene-Phenotype Associations

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

nerve-tissue-proteins Gene Set

From Phosphosite Textmining Biological Term Annotations

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

soft tissue sarcoma cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

connective tissue Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

brown adipose tissue Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

synovial tissue Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

adipose tissue Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

white adipose tissue Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

abdominal adipose tissue Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

vascular tissue Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

lymphoid tissue Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

rheumatoid arthritis disease specific synovial tissue Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue rheumatoid arthritis disease specific synovial tissue from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

connective tissue Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

vascular tissue Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

lymphoid tissue Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

adipose tissue Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

brown adipose tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

storage tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

supportive connective tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

extraembryonic tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

tissue culture Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

soft tissue sarcoma cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

rheumatoid arthritis disease specific synovial tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue rheumatoid arthritis disease specific synovial tissue in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

trophosome tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

connective tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

soft tissue sarcoma cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

intramuscular adipose tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

ulcer tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

subcutaneous tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

periurethral tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

lymphoid tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

granulation tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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