Name

Cardiac Conduction Defect Gene Set

From CTD Gene-Disease Associations

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

atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Cardiac conduction defect, nonspecific Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiac conduction defect, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

cardiac conduction defect, nonspecific Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiac conduction defect, nonspecific phenotype from the curated OMIM Gene-Disease Associations dataset.

{cardiac conduction defect, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {cardiac conduction defect, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac conduction disturbances and degenerative changes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac conduction disturbances and degenerative changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

positive regulation of cardiac conduction Gene Set

From GO Biological Process Annotations

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

regulation of heart rate by cardiac conduction Gene Set

From GO Biological Process Annotations

genes participating in the regulation of heart rate by cardiac conduction biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cell communication by electrical coupling involved in cardiac conduction Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cell communication by electrical coupling involved in cardiac conduction biological process from the curated GO Biological Process Annotations dataset.

cell-cell signaling involved in cardiac conduction Gene Set

From GO Biological Process Annotations

genes participating in the cell-cell signaling involved in cardiac conduction biological process from the curated GO Biological Process Annotations dataset.

cardiac conduction Gene Set

From GO Biological Process Annotations

genes participating in the cardiac conduction biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac conduction Gene Set

From GO Biological Process Annotations

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

cell communication involved in cardiac conduction Gene Set

From GO Biological Process Annotations

genes participating in the cell communication involved in cardiac conduction biological process from the curated GO Biological Process Annotations dataset.

cell communication by electrical coupling involved in cardiac conduction Gene Set

From GO Biological Process Annotations

genes participating in the cell communication by electrical coupling involved in cardiac conduction biological process from the curated GO Biological Process Annotations dataset.

regulation of the force of heart contraction by cardiac conduction Gene Set

From GO Biological Process Annotations

genes participating in the regulation of the force of heart contraction by cardiac conduction biological process from the curated GO Biological Process Annotations dataset.

regulation of cell communication by electrical coupling involved in cardiac conduction Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cell communication by electrical coupling involved in cardiac conduction biological process from the curated GO Biological Process Annotations dataset.

cardiac conduction system development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac conduction system development biological process from the curated GO Biological Process Annotations dataset.

gap junction channel activity involved in cardiac conduction electrical coupling Gene Set

From GO Molecular Function Annotations

genes performing the gap junction channel activity involved in cardiac conduction electrical coupling molecular function from the curated GO Molecular Function Annotations dataset.

?cardiac conduction disease with or without dilated cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cardiac conduction disease with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.

atrial septal defect 7, with or without av conduction defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmias, cardiac; brugada syndrome; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; brugada syndrome; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac death; cardiac morbidity Gene Set

From GAD Gene-Disease Associations

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

death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; heart diseases; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; heart diseases; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; myocardial ischemia; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; myocardial ischemia; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; diabetes mellitus; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; diabetes mellitus; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; death, sudden, cardiac; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac muscle cell-cardiac muscle cell adhesion Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle cell-cardiac muscle cell adhesion biological process from the curated GO Biological Process Annotations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

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

cardiac defects Gene Set

From GAD Gene-Disease Associations

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

hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From OMIM Gene-Disease Associations

genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

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

cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism Gene Set

From GAD Gene-Disease Associations

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

congenital heart defects; heart defects, congenital; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; heart septal defects, atrial; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; heart septal defects, atrial; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal 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.

body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Slowed nerve conduction velocity, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Slowed nerve conduction velocity, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Slowed Nerve Conduction Velocity, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Slowed Nerve Conduction Velocity, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

heart conduction disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

heart conduction disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

heart conduction disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

electrocardiographic conduction measures Gene Set

From GAD Gene-Disease Associations

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

normal nerve conduction Gene Set

From GAD Gene-Disease Associations

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

conduction Gene Set

From GeneRIF Biological Term Annotations

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

Electrocardiographic conduction measures Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Electrocardiographic conduction measures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Atrioventricular conduction Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

heart conduction disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormal atrioventricular conduction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal motor nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

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

abnormal atrioventricular conduction Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal atrioventricular conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased sensory nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal sensory nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased motor nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of peripheral nerve conduction Gene Set

From HPO Gene-Disease Associations

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

Bone Conduction Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

decreased nerve conduction velocity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased nerve conduction velocity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal atrioventricular node conduction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal atrioventricular node conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal nerve conduction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal nerve conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal atrioventricular bundle conduction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal atrioventricular bundle conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sinoatrial node conduction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sinoatrial node conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal impulse conducting system conduction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal impulse conducting system conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased nerve conduction velocity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased nerve conduction velocity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

?slowed nerve conduction velocity, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?slowed nerve conduction velocity, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

hop pathway in cardiac development Gene Set

From Biocarta Pathways

proteins participating in the hop pathway in cardiac development pathway from the Biocarta Pathways dataset.

cardiac protection against ros Gene Set

From Biocarta Pathways

proteins participating in the cardiac protection against ros pathway from the Biocarta Pathways dataset.

role of egf receptor transactivation by gpcrs in cardiac hypertrophy Gene Set

From Biocarta Pathways

proteins participating in the role of egf receptor transactivation by gpcrs in cardiac hypertrophy pathway from the Biocarta Pathways dataset.

alk in cardiac myocytes Gene Set

From Biocarta Pathways

proteins participating in the alk in cardiac myocytes pathway from the Biocarta Pathways dataset.

GM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the GM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Sudden cardiac death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sudden cardiac death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiac valvular dysplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiac valvular dysplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiac arrest Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiac arrest phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiac arrhythmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiac arrhythmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiac Glycosides Gene Set

From CTD Gene-Chemical Interactions

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

Cardiac valvular dysplasia, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac valvular dysplasia, X-linked from the curated CTD Gene-Disease Associations dataset.

Edema, Cardiac Gene Set

From CTD Gene-Disease Associations

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

Cardiac Output, Low Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac Output, Low from the curated CTD Gene-Disease Associations dataset.

Arrhythmias, Cardiac Gene Set

From CTD Gene-Disease Associations

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

Death, Sudden, Cardiac Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Death, Sudden, Cardiac from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos syndrome, cardiac valvular form Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos syndrome, cardiac valvular form from the curated CTD Gene-Disease Associations dataset.

Cardiac Arrhythmia, Ankyrin-B-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac Arrhythmia, Ankyrin-B-Related from the curated CTD Gene-Disease Associations dataset.

Cardiac Output, High Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac Output, High from the curated CTD Gene-Disease Associations dataset.

Cardiac Tamponade Gene Set

From CTD Gene-Disease Associations

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

Sinus Arrest, Cardiac Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sinus Arrest, Cardiac from the curated CTD Gene-Disease Associations dataset.

Arrhythmias, Cardiac Gene Set

From dbGAP Gene-Trait Associations

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

Death, Sudden, Cardiac Gene Set

From dbGAP Gene-Trait Associations

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

cardiac sarcoidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cardiac tamponade Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

myocardial infarct; cardiac death Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac function Gene Set

From GAD Gene-Disease Associations

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

heart disease, ischemic; myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inherited cardiac arrhythmia long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inherited cardiac arrhythmia long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac death Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart rate; arrhythmia, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart rate; arrhythmia, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

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

sudden cardiac death Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

congenital cardiac malformations Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; heart failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; heart failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac output, low Gene Set

From GAD Gene-Disease Associations

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

coronary disease; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; Gene Set

From GAD Gene-Disease Associations

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

cardiac arrhythmias and sudden death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac arrhythmias and sudden death 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.

accelerated idioventricular rhythm; arrhythmias, cardiac; myocardial infarction; reperfusion injury; tachycardia, ventricular; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease accelerated idioventricular rhythm; arrhythmias, cardiac; myocardial infarction; reperfusion injury; tachycardia, ventricular; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac repolarization. Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; heart arrest; long qt syndrome; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; heart arrest; long qt syndrome; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; heart diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; heart diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadaver; cardiovascular diseases; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadaver; cardiovascular diseases; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

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

death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac sarcoidosis Gene Set

From GAD Gene-Disease Associations

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

sudden cardiac arrest risk Gene Set

From GAD Gene-Disease Associations

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

cardiac and cutaneous amyloidosis Gene Set

From GAD Gene-Disease Associations

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

esophageal cancer; gastric cardiac cancer Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; death, sudden; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; ventricular premature complexes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; ventricular premature complexes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; hypertrophy, left ventricular; leopard syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; hypertrophy, left ventricular; leopard syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac autonomic responsiveness Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal cancer; cardiac cancer Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; heart failure; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; heart failure; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac structure and function Gene Set

From GAD Gene-Disease Associations

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

cardiac growth Gene Set

From GAD Gene-Disease Associations

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

cardiac output, low; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac output, low; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac stroke volume to regular exercise Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac stroke volume to regular exercise in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmia, cardiac Gene Set

From GAD Gene-Disease Associations

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

cardiac disease Gene Set

From GAD Gene-Disease Associations

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

transplant associated vasculopathy after cardiac transplantation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease transplant associated vasculopathy after cardiac transplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bleeding after cardiac surgery Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal cancer and gastric cardiac carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophageal cancer and gastric cardiac carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; brugada syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac Gene Set

From GeneRIF Biological Term Annotations

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

Cardiac Hypertrophy_Myocardial tissue_GSE5500 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Cardiac Hypertrophy_Myocardial tissue_GSE5500 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Cardiac Failure_Myocardial tissue_GSE1988 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Cardiac Failure_Myocardial tissue_GSE1988 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Cardiac Hypertrophy_Myocardial tissue_GSE1621 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Cardiac Hypertrophy_Myocardial tissue_GSE1621 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

TMEM88_KD_GSE43805_682_human_hES cells differentiated along the cardiac lineage Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the TMEM88_KD_GSE43805_682_human_hES cells differentiated along the cardiac lineage gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

regulation of cardiac muscle cell myoblast differentiation Gene Set

From GO Biological Process Annotations

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

positive regulation of cardiac muscle hypertrophy in response to stress Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cardiac muscle adaptation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cardiac muscle adaptation 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.

regulation of atrial cardiac muscle cell membrane depolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of atrial cardiac muscle cell membrane depolarization biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cardiac muscle fiber development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cardiac muscle fiber 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.

cardiac muscle cell action potential involved in contraction Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle cell action potential involved in contraction 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.

cardiac ventricle formation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac ventricle formation biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

cardiac chamber development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac chamber development biological process from the curated GO Biological Process Annotations dataset.

cardiac septum development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac septum development biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle hypertrophy in response to stress Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations dataset.

cardiac cell fate determination Gene Set

From GO Biological Process Annotations

genes participating in the cardiac cell fate determination biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in cardiac muscle cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in cardiac muscle cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle fiber development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle fiber development biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac vascular smooth muscle cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac vascular smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle contraction Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle contraction biological process from the curated GO Biological Process Annotations dataset.

cardiac right atrium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac right atrium morphogenesis 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.

regulation of cardiac cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac cell fate specification biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle contraction by calcium ion signaling Gene Set

From GO Biological Process Annotations

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

cardiac cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the cardiac cell fate specification biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

regulation of planar cell polarity pathway involved in cardiac right atrium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of planar cell polarity pathway involved in cardiac right atrium morphogenesis biological process from the curated GO Biological Process Annotations dataset.

purkinje myocyte to ventricular cardiac muscle cell communication Gene Set

From GO Biological Process Annotations

genes participating in the purkinje myocyte to ventricular cardiac muscle cell communication biological process from the curated GO Biological Process Annotations dataset.

regulation of membrane depolarization during cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the regulation of membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac vascular smooth muscle cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac vascular smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac cell fate specification biological process from the curated GO Biological Process Annotations dataset.

cardiac myofibril assembly Gene Set

From GO Biological Process Annotations

genes participating in the cardiac myofibril assembly biological process from the curated GO Biological Process Annotations dataset.

cardiac pacemaker cell development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac pacemaker cell development biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle fiber development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle fiber development biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle adaptation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle adaptation biological process from the curated GO Biological Process Annotations dataset.

cardiac chamber formation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac chamber formation biological process from the curated GO Biological Process Annotations dataset.

cardiac atrium formation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac atrium formation biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle adaptation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle adaptation biological process from the curated GO Biological Process Annotations dataset.

regulation of ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the regulation of ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

negative regulation of relaxation of cardiac muscle Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of relaxation of cardiac muscle biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle cell contraction Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle cell contraction biological process from the curated GO Biological Process Annotations dataset.

atrial cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the atrial cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle cell differentiation Gene Set

From GO Biological Process Annotations

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

positive regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac chamber formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac chamber formation 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.

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.

negative regulation of cardiac muscle cell apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac muscle cell apoptotic process biological process from the curated GO Biological Process Annotations dataset.

atrial cardiac muscle cell development Gene Set

From GO Biological Process Annotations

genes participating in the atrial cardiac muscle cell development biological process from the curated GO Biological Process Annotations dataset.

cardiac cell development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac cell development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac muscle cell myoblast differentiation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac muscle cell myoblast differentiation biological process from the curated GO Biological Process Annotations dataset.

regulation of relaxation of cardiac muscle Gene Set

From GO Biological Process Annotations

genes participating in the regulation of relaxation of cardiac muscle biological process from the curated GO Biological Process Annotations dataset.

cardiac right ventricle morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac right ventricle morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of atrial cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the regulation of atrial cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle cell proliferation 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.

regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations dataset.

cardiac vascular smooth muscle cell development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac vascular smooth muscle cell development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cardiac muscle cell apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cardiac muscle cell apoptotic process 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.

positive regulation of cardiac muscle cell differentiation Gene Set

From GO Biological Process Annotations

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

cardiac epithelial to mesenchymal transition Gene Set

From GO Biological Process Annotations

genes participating in the cardiac epithelial to mesenchymal transition 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.

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.

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.

cardiac neural crest cell migration involved in outflow tract morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of relaxation of cardiac muscle Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of relaxation of cardiac muscle biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac muscle hypertrophy Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac muscle hypertrophy biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac muscle adaptation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac muscle adaptation biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac chamber morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac chamber morphogenesis biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle thin filament assembly Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle thin filament assembly 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 cardiac muscle cell contraction Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle cell contraction biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in cardiac neural crest cell differentiation involved in heart development Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in cardiac neural crest cell differentiation involved in heart development biological process from the curated GO Biological Process Annotations dataset.

atrial cardiac muscle cell to av node cell communication Gene Set

From GO Biological Process Annotations

genes participating in the atrial cardiac muscle cell to av node cell communication 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.

ventricular cardiac muscle cell differentiation Gene Set

From GO Biological Process Annotations

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

regulation of cardiac muscle cell apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle cell apoptotic process biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle cell membrane potential Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle cell membrane potential 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.

cardiac muscle cell myoblast differentiation Gene Set

From GO Biological Process Annotations

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

regulation of cardiac muscle hypertrophy Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle hypertrophy biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle cell proliferation biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle hypertrophy Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle hypertrophy biological process from the curated GO Biological Process Annotations dataset.

regulation of cell growth involved in cardiac muscle cell development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cell growth involved in cardiac muscle cell development biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle contraction Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle contraction 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.

regulation of cardiac muscle cell action potential involved in regulation of contraction Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle cell action potential involved in regulation of contraction biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

regulation of ventricular cardiac muscle cell membrane depolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of ventricular cardiac muscle cell membrane depolarization biological process from the curated GO Biological Process Annotations dataset.

cardiac vascular smooth muscle cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac vascular smooth muscle cell differentiation 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.

canonical wnt signaling pathway involved in positive regulation of cardiac outflow tract cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in positive regulation of cardiac outflow tract cell proliferation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac muscle cell differentiation Gene Set

From GO Biological Process Annotations

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

regulation of cardiac muscle cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle cell differentiation 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.

cardiac neural crest cell development involved in heart development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac neural crest cell development involved in heart development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cell growth involved in cardiac muscle cell development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cell growth involved in cardiac muscle cell development biological process from the curated GO Biological Process Annotations dataset.

planar cell polarity pathway involved in cardiac right atrium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the planar cell polarity pathway involved in cardiac right atrium morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac chamber morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac chamber morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac muscle hypertrophy in response to stress Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations dataset.

cell growth involved in cardiac muscle cell development Gene Set

From GO Biological Process Annotations

genes participating in the cell growth involved in cardiac muscle cell development 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.

cardiac ventricle development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac ventricle development biological process from the curated GO Biological Process Annotations dataset.

relaxation of cardiac muscle Gene Set

From GO Biological Process Annotations

genes participating in the relaxation of cardiac muscle biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cell growth involved in cardiac muscle cell development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cell growth involved in cardiac muscle cell development biological process from the curated GO Biological Process Annotations dataset.

regulation of cardiac chamber formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cardiac chamber formation biological process from the curated GO Biological Process Annotations dataset.

regulation of canonical wnt signaling pathway involved in cardiac muscle cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the regulation of canonical wnt signaling pathway involved in cardiac muscle cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cardiac muscle cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cardiac muscle cell proliferation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations dataset.

positive regulation of canonical wnt signaling pathway involved in cardiac muscle cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of canonical wnt signaling pathway involved in cardiac muscle cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle cell apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle cell apoptotic process 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.

positive regulation of cardiac vascular smooth muscle cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cardiac vascular smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations dataset.

cardiac pacemaker cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the cardiac pacemaker cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

cardiac left ventricle morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac left ventricle morphogenesis biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac myofibril assembly Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac myofibril assembly biological process from the curated GO Biological Process Annotations dataset.

cardiac neural crest cell development involved in outflow tract morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac neural crest cell development involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations dataset.

cardiac pacemaker cell differentiation Gene Set

From GO Biological Process Annotations

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

purkinje myocyte to ventricular cardiac muscle cell signaling Gene Set

From GO Biological Process Annotations

genes participating in the purkinje myocyte to ventricular cardiac muscle cell signaling biological process from the curated GO Biological Process Annotations dataset.

cardiac right ventricle formation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac right ventricle formation biological process from the curated GO Biological Process Annotations dataset.

cardiac chamber morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac chamber morphogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of membrane depolarization during cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

negative regulation of canonical wnt signaling pathway involved in cardiac muscle cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of canonical wnt signaling pathway involved in cardiac muscle cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

sa node cell to atrial cardiac muscle cell communication Gene Set

From GO Biological Process Annotations

genes participating in the sa node cell to atrial cardiac muscle cell communication biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac muscle cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac muscle cell proliferation biological process from the curated GO Biological Process Annotations dataset.

cardiac septum morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac septum morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac muscle hypertrophy in response to stress Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations dataset.

cardiac atrium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac atrium morphogenesis biological process from the curated GO Biological Process Annotations dataset.

membrane repolarization during cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

regulation of ventricular cardiac muscle cell membrane repolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of ventricular cardiac muscle cell membrane repolarization biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle cell development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle cell development biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac muscle cell development Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac muscle cell development biological process from the curated GO Biological Process Annotations dataset.

cardiac cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the cardiac cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

cardiac left ventricle formation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac left ventricle formation biological process from the curated GO Biological Process Annotations dataset.

regulation of atrial cardiac muscle cell membrane repolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of atrial cardiac muscle cell membrane repolarization biological process from the curated GO Biological Process Annotations dataset.

cardiac muscle cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the cardiac muscle cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

cardiac ventricle morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac ventricle morphogenesis 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.

cardiac endothelial cell differentiation Gene Set

From GO Biological Process Annotations

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

positive regulation of cardiac muscle hypertrophy Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cardiac muscle hypertrophy biological process from the curated GO Biological Process Annotations dataset.

negative regulation of planar cell polarity pathway involved in cardiac right atrium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of planar cell polarity pathway involved in cardiac right atrium morphogenesis biological process from the curated GO Biological Process Annotations dataset.

membrane depolarization during cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cardiac muscle contraction Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cardiac muscle contraction biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cardiac muscle contraction Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cardiac muscle contraction biological process from the curated GO Biological Process Annotations dataset.

voltage-gated sodium channel activity involved in cardiac muscle cell action potential Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated sodium channel activity involved in cardiac muscle cell action potential molecular function from the curated GO Molecular Function Annotations dataset.

calcium:sodium antiporter activity involved in regulation of cardiac muscle cell membrane potential Gene Set

From GO Molecular Function Annotations

genes performing the calcium:sodium antiporter activity involved in regulation of cardiac muscle cell membrane potential molecular function from the curated GO Molecular Function Annotations dataset.

sodium:proton antiporter activity involved in regulation of cardiac muscle cell membrane potential Gene Set

From GO Molecular Function Annotations

genes performing the sodium:proton antiporter activity involved in regulation of cardiac muscle cell membrane potential molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated potassium channel activity involved in cardiac muscle cell action potential repolarization Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated potassium channel activity involved in cardiac muscle cell action potential repolarization molecular function from the curated GO Molecular Function Annotations dataset.

calcium-transporting atpase activity involved in regulation of cardiac muscle cell membrane potential Gene Set

From GO Molecular Function Annotations

genes performing the calcium-transporting atpase activity involved in regulation of cardiac muscle cell membrane potential molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated potassium channel activity involved in atrial cardiac muscle cell action potential repolarization Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated potassium channel activity involved in atrial cardiac muscle cell action potential repolarization molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated calcium channel activity involved in cardiac muscle cell action potential Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated calcium channel activity involved in cardiac muscle cell action potential molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization molecular function from the curated GO Molecular Function Annotations dataset.

Cardiac hypertrophy Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Cardiac repolarization Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Sudden cardiac arrest Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Sudden cardiac arrest phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Cardiac muscle measurement Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Cardiac muscle measurement phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Cardiac structure and function Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Cardiac structure and function phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Cardiac Troponin-T levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

sudden cardiac death Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sudden cardiac death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiac ventricle Gene Set

From GWASdb SNP-Phenotype Associations

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

cardiac arrest Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the cardiac arrest phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiac morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

cardiac valve calcification Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the cardiac valve calcification phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiac ventricle Gene Set

From HPO Gene-Disease Associations

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

cardiac arrest Gene Set

From HPO Gene-Disease Associations

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

abnormality of cardiac morphology Gene Set

From HPO Gene-Disease Associations

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

cardiac fibroma Gene Set

From HPO Gene-Disease Associations

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

sudden cardiac death Gene Set

From HPO Gene-Disease Associations

genes associated with the sudden cardiac death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cardiac atrium Gene Set

From HPO Gene-Disease Associations

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

cardiac valve calcification Gene Set

From HPO Gene-Disease Associations

genes associated with the cardiac valve calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cardiac shunt Gene Set

From HPO Gene-Disease Associations

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

abnormal connection of the cardiac segments Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal connection of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the cardiac septa Gene Set

From HPO Gene-Disease Associations

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

cardiac rhabdomyoma Gene Set

From HPO Gene-Disease Associations

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

abnormal spatial orientation of the cardiac segments Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal spatial orientation of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cardiac myxoma Gene Set

From HPO Gene-Disease Associations

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

Cardiac Output, Low Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Cardiac Output, Low phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Arrhythmias, Cardiac Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Death, Sudden, Cardiac Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Death, Sudden, Cardiac phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Out-of-Hospital Cardiac Arrest Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Out-of-Hospital Cardiac Arrest phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

cardiac interstitial fibrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cardiac interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cardiac ischemia Gene Set

From MPO Gene-Phenotype Associations

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

cardiac fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

cardiac muscle necrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cardiac muscle necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac jelly morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to dystrophic cardiac calcinosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to dystrophic cardiac calcinosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cardiac output Gene Set

From MPO Gene-Phenotype Associations

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

decreased cardiac stroke volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cardiac stroke volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cardiac stroke volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cardiac stroke volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac mesenchyme morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cardiac output Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac output phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cardiac jelly Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cardiac neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac epithelial to mesenchymal transition Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac epithelial to mesenchymal transition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cardiac hypertrophy Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cardiac valve physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac valve physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac stroke volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac stroke volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cardiac neural crest cells Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cardiac muscle relaxation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac muscle relaxation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased cardiac muscle contractility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cardiac muscle contractility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired cardiac neural crest cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired cardiac neural crest cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased cardiac muscle contractility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cardiac muscle contractility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac muscle contractility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac muscle contractility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cardiac output Gene Set

From MPO Gene-Phenotype Associations

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

cardiac muscle degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cardiac muscle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to dystrophic cardiac calcinosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to dystrophic cardiac calcinosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dystrophic cardiac calcinosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dystrophic cardiac calcinosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac cell glucose uptake Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac cell glucose uptake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal stomach cardiac region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal stomach cardiac region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cardiac edema Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cardiac edema 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.

decreased cardiac neural crest cell number Gene Set

From MPO Gene-Phenotype Associations

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

absent cardiac desmosomes Gene Set

From MPO Gene-Phenotype Associations

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

cardiac valve regurgitation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cardiac valve regurgitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

t-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the t-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiac arrhythmia, ankyrin-b-related Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiac arrhythmia, ankyrin-b-related phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, cardiac valvular form Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, cardiac valvular form phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiac valvular dysplasia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiac valvular dysplasia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

fabry disease, cardiac variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the fabry disease, cardiac variant phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiac Gene Set

From Phosphosite Textmining Biological Term Annotations

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

myocytes-cardiac Gene Set

From Phosphosite Textmining Biological Term Annotations

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

cardiac muscle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

cardiac muscle Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

human cardiac microvascular endothelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cardiac muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cardiac muscle cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cardiac stomach Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cardiac purkinje cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cardiac purkinje fiber Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cardiac muscle fiber Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

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

From Wikipathways Pathways

proteins participating in the Regulation of Cardiac Hypertrophy by miR-208(Mus musculus) pathway from the Wikipathways Pathways dataset.

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

From Wikipathways Pathways

proteins participating in the miR-1 in cardiac development(Mus musculus) pathway from the Wikipathways Pathways dataset.

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

From Wikipathways Pathways

proteins participating in the Calcium Regulation in the Cardiac Cell(Mus musculus) pathway from the Wikipathways Pathways dataset.

Calcium Regulation in the Cardiac Cell(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Calcium Regulation in the Cardiac Cell(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Cardiac Hypertrophic Response(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Cardiac Hypertrophic Response(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Cardiac Progenitor Differentiation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Cardiac Progenitor Differentiation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

TFs Regulate miRNAs related to cardiac hypertrophy(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the TFs Regulate miRNAs related to cardiac hypertrophy(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Dandy-Walker like malformation with atrioventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Protan defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Protan defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Forebrain defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Forebrain defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

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

Neutral 1 amino acid transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neutral 1 amino acid transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Ventricular septal defect 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular septal defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular septal defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Laron-type isolated somatotropin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Laron-type isolated somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neural tube defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart defects, multiple types, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucose-6-phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iodotyrosine deiodination defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iodotyrosine deiodination defect 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.

Renal carnitine transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect 5 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.

Erythrocyte lactate transporter defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythrocyte lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 3 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 defect of folate absorption Gene Set

From ClinVar Gene-Phenotype Associations

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

Oocyte maturation defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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.

Iodotyrosyl coupling defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iodotyrosyl coupling defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heart Septal Defects, Ventricular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects, Ventricular from the curated CTD Gene-Disease 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.

Combined Cellular And Humoral Immune Defects With Granulomas Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.

Sacral defect and anterior sacral meningocele Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.

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.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.

Atrial septal defect 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial septal defect 2 from the curated CTD Gene-Disease Associations dataset.

ATRIOVENTRICULAR SEPTAL DEFECT 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIOVENTRICULAR SEPTAL DEFECT 3 from the curated CTD Gene-Disease Associations dataset.

Heart Septal Defects Gene Set

From CTD Gene-Disease Associations

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

Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 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.

Atrial Septal Defect 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 4 from the curated CTD Gene-Disease Associations dataset.

Neural Tube Defects Gene Set

From CTD Gene-Disease Associations

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

Atrioventricular Canal Defect Gene Set

From CTD Gene-Disease Associations

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

Bile acid synthesis defect, congenital, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 1 from the curated CTD Gene-Disease Associations dataset.

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Neural tube defect, folate-sensitive Gene Set

From CTD Gene-Disease Associations

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

Atrial Septal Defect 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 6 from the curated CTD Gene-Disease Associations dataset.

Laterality Defects, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Laterality Defects, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT 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.

Heart Septal Defects, Atrial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects, Atrial from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 5 from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 1 from the curated CTD Gene-Disease Associations dataset.

Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset.

Erythrocyte Lactate Transporter Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Erythrocyte Lactate Transporter Defect from the curated CTD Gene-Disease Associations dataset.

Heart Defects, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Defects, Congenital from the curated CTD Gene-Disease Associations dataset.

Micronuclei, Chromosome-Defective Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Micronuclei, Chromosome-Defective from the curated CTD Gene-Disease Associations dataset.

Color Vision Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Color Vision Defects 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.

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.

atrial heart septal defect Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease atrial heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

heart septal defect Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alcohol-related birth defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

atrioventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital bile acid synthesis defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atrial heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

qualitative platelet defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

defective colour vision Gene Set

From GAD Gene-Disease Associations

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

micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

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

congenital heart defects Gene Set

From GAD Gene-Disease Associations

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

heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

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

cleft palate and calvaria defects. Gene Set

From GAD Gene-Disease Associations

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

familial defective apolipoprotein b100. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial defective apolipoprotein b100. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; dihydropyrimidine dehydrogenase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; dihydropyrimidine dehydrogenase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

defective dr beta 4 chain expression to the hla-drb1 gene Gene Set

From GAD Gene-Disease Associations

genes associated with the disease defective dr beta 4 chain expression to the hla-drb1 gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial defective apolipoprotein b Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; micronuclei, chromosome-defective 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 defects Gene Set

From GAD Gene-Disease Associations

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

down syndrome; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dilatation, pathologic; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dilatation, pathologic; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; lung neoplasms; micronuclei, chromosome-defective; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; lung neoplasms; micronuclei, chromosome-defective; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathies; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathies; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial defective apolipoprotein b-100 in a chinese man Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial defective apolipoprotein b-100 in a chinese man in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; heart septal defects Gene Set

From GAD Gene-Disease Associations

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

axial skeletal defects Gene Set

From GAD Gene-Disease Associations

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

left-right laterality defects Gene Set

From GAD Gene-Disease Associations

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

heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

human spermatogenic defect Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects and preeclampsia Gene Set

From GAD Gene-Disease Associations

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

neural tube defects Gene Set

From GAD Gene-Disease Associations

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

color vision defects; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, atrial; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, atrial; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

defective heparin binding associated Gene Set

From GAD Gene-Disease Associations

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

flushing; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease flushing; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital Gene Set

From GAD Gene-Disease Associations

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

neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; heart defects, congenital; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; heart defects, congenital; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ductus arteriosus, patent; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ductus arteriosus, patent; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

visual field defects Gene Set

From GAD Gene-Disease Associations

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

heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital goiter and defective tg synthesis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital goiter and defective tg synthesis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects Gene Set

From GAD Gene-Disease Associations

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

heart septal defects, ventricular; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

defectiveness Gene Set

From GeneRIF Biological Term Annotations

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

defects Gene Set

From GeneRIF Biological Term Annotations

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

defectsaffected Gene Set

From GeneRIF Biological Term Annotations

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

defective Gene Set

From GeneRIF Biological Term Annotations

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

defect Gene Set

From GeneRIF Biological Term Annotations

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

Conotruncal heart defects Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Conotruncal heart defects phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

conotruncal defect Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the conotruncal defect phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

thyroid hormone receptor defect Gene Set

From HPO Gene-Disease Associations

genes associated with the thyroid hormone receptor defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive visual field defects Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive visual field defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midline defect of mandible Gene Set

From HPO Gene-Disease Associations

genes associated with the midline defect of mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

electron transfer flavoprotein-ubiquinone oxidoreductase defect Gene Set

From HPO Gene-Disease Associations

genes associated with the electron transfer flavoprotein-ubiquinone oxidoreductase defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

secundum atrial septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the secundum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lung segmentation defects Gene Set

From HPO Gene-Disease Associations

genes associated with the lung segmentation defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dynein arm defect of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the dynein arm defect of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inlet ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the inlet ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thyroid defect in oxidation and organification of iodide Gene Set

From HPO Gene-Disease Associations

genes associated with the thyroid defect in oxidation and organification of iodide phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adrenocorticotropin (acth) receptor (acthr) defect Gene Set

From HPO Gene-Disease Associations

genes associated with the adrenocorticotropin (acth) receptor (acthr) defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sacral segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the sacral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulmonary valve defects Gene Set

From HPO Gene-Disease Associations

genes associated with the pulmonary valve defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abdominal wall defect Gene Set

From HPO Gene-Disease Associations

genes associated with the abdominal wall defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

visual field defect Gene Set

From HPO Gene-Disease Associations

genes associated with the visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

defective dna repair after ultraviolet radiation damage Gene Set

From HPO Gene-Disease Associations

genes associated with the defective dna repair after ultraviolet radiation damage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial respiratory chain defects Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial respiratory chain defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

defective lymphocyte apoptosis Gene Set

From HPO Gene-Disease Associations

genes associated with the defective lymphocyte apoptosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

symmetrical, oval parietal bone defects Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetrical, oval parietal bone defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrioventricular canal defect with right ventricle aorta and pulmonary atresia Gene Set

From HPO Gene-Disease Associations

genes associated with the atrioventricular canal defect with right ventricle aorta and pulmonary atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

defective b cell activation Gene Set

From HPO Gene-Disease Associations

genes associated with the defective b cell activation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

defect in the atrial septum Gene Set

From HPO Gene-Disease Associations

genes associated with the defect in the atrial septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the toes 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.

congenital septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skull defect Gene Set

From HPO Gene-Disease Associations

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

osteolytic defects of the hand bones Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the hand bones 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.

forearm reduction defects Gene Set

From HPO Gene-Disease Associations

genes associated with the forearm reduction defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cervical segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the cervical segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrioventricular canal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

perimembranous ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the perimembranous ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midline defect of the nose Gene Set

From HPO Gene-Disease Associations

genes associated with the midline defect of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

asymmetric, linear skin defects Gene Set

From HPO Gene-Disease Associations

genes associated with the asymmetric, linear skin defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

complete atrioventricular canal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the complete atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

defective dehydrogenation of isovaleryl coa and butyryl coa Gene Set

From HPO Gene-Disease Associations

genes associated with the defective dehydrogenation of isovaleryl coa and butyryl coa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

defective b cell differentiation Gene Set

From HPO Gene-Disease Associations

genes associated with the defective b cell differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

large central visual field defect Gene Set

From HPO Gene-Disease Associations

genes associated with the large central visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

conotruncal defect Gene Set

From HPO Gene-Disease Associations

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

primum atrial septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the primum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Heart Septal Defects, Ventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects, Ventricular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Endocardial Cushion Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Heart Defects, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Defects, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Color Vision Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Heart Septal Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Heart Septal Defects, Atrial Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects, Atrial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Micronuclei, Chromosome-Defective Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Micronuclei, Chromosome-Defective phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Neural Tube Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mannose-P-dolichol utilization defect 1 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mannose-P-dolichol utilization defect 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Defective-in-cullin neddylation protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Defective-in-cullin neddylation protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

defective assembly of class i molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the defective assembly of class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

perimembraneous ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

defective assembly of class ii molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the defective assembly of class ii molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

partial atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

inlet ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

double outlet right ventricle with atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

iodide oxidation defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aorticopulmonary septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

double outlet right ventricle, ventricular defect committed to aorta Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscular ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ostium primum atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

complete atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ostium secundum atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

defective intracellular transport of class i molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the defective intracellular transport of class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype 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.

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation 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.

schizophrenia, neurophysiologic defect in Gene Set

From OMIM Gene-Disease Associations

genes associated with the schizophrenia, neurophysiologic defect in 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.

{atrioventricular septal defect, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {atrioventricular septal defect, susceptibility to, 1} 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.

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.

{neural tube defects, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

erythrocyte lactate transporter defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the erythrocyte lactate transporter defect phenotype from the curated OMIM Gene-Disease Associations dataset.

natural killer cell and glucocorticoid deficiency with dna repair defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the natural killer cell and glucocorticoid deficiency with dna repair defect phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

forebrain defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the forebrain defects phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, nonsyndromic, 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

selective t-cell defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the selective t-cell defect 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.

atrial septal defect 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

?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.

left ventricular noncompaction 1, with or without congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 1, with or without congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

combined cellular and humoral immune defects with granulomas Gene Set

From OMIM Gene-Disease Associations

genes associated with the combined cellular and humoral immune defects with granulomas phenotype from the curated OMIM Gene-Disease Associations dataset.

neural tube defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the neural tube defects phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia, neurologic defects, and endocrinopathy syndrome 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.

{atrioventricular septal defect, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {atrioventricular septal defect, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, congenital heart defects, and posterior embryotoxon Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated OMIM Gene-Disease Associations dataset.

oocyte maturation defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the oocyte maturation defect 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.

atrioventricular septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 5 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.

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.

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.

immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia 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.

congenital heart defects, nonsyndromic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

pancreatic agenesis and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the pancreatic agenesis and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects 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.

Defective PAPSS2 causes SEMD-PA Gene Set

From Reactome Pathways

proteins participating in the Defective PAPSS2 causes SEMD-PA pathway from the Reactome Pathways dataset.

Defective FMO3 causes Trimethylaminuria (TMAU) Gene Set

From Reactome Pathways

proteins participating in the Defective FMO3 causes Trimethylaminuria (TMAU) pathway from the Reactome Pathways dataset.

Defective MAOA causes Brunner syndrome (BRUNS) Gene Set

From Reactome Pathways

proteins participating in the Defective MAOA causes Brunner syndrome (BRUNS) pathway from the Reactome Pathways dataset.

Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3) pathway from the Reactome Pathways dataset.

Defective ALG8 causes ALG8-CDG (CDG-1h) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG8 causes ALG8-CDG (CDG-1h) pathway from the Reactome Pathways dataset.

Defective MGAT2 causes MGAT2-CDG (CDG-2a) Gene Set

From Reactome Pathways

proteins participating in the Defective MGAT2 causes MGAT2-CDG (CDG-2a) pathway from the Reactome Pathways dataset.

Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) pathway from the Reactome Pathways dataset.

Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC Gene Set

From Reactome Pathways

proteins participating in the Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC pathway from the Reactome Pathways dataset.

Defective MMAB causes methylmalonic aciduria type cblB Gene Set

From Reactome Pathways

proteins participating in the Defective MMAB causes methylmalonic aciduria type cblB pathway from the Reactome Pathways dataset.

Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) pathway from the Reactome Pathways dataset.

Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) Gene Set

From Reactome Pathways

proteins participating in the Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) pathway from the Reactome Pathways dataset.

Defective CYP19A1 causes Aromatase excess syndrome (AEXS) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP19A1 causes Aromatase excess syndrome (AEXS) pathway from the Reactome Pathways dataset.

Defective ACY1 causes encephalopathy Gene Set

From Reactome Pathways

proteins participating in the Defective ACY1 causes encephalopathy pathway from the Reactome Pathways dataset.

Defects in cobalamin (B12) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in cobalamin (B12) metabolism pathway from the Reactome Pathways dataset.

Defective CYP1B1 causes Glaucoma Gene Set

From Reactome Pathways

proteins participating in the Defective CYP1B1 causes Glaucoma pathway from the Reactome Pathways dataset.

Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B) pathway from the Reactome Pathways dataset.

Defective AMN causes hereditary megaloblastic anemia 1 Gene Set

From Reactome Pathways

proteins participating in the Defective AMN causes hereditary megaloblastic anemia 1 pathway from the Reactome Pathways dataset.

Defective RFT1 causes RFT1-CDG (CDG-1n) Gene Set

From Reactome Pathways

proteins participating in the Defective RFT1 causes RFT1-CDG (CDG-1n) pathway from the Reactome Pathways dataset.

Defective ALG6 causes ALG6-CDG (CDG-1c) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG6 causes ALG6-CDG (CDG-1c) pathway from the Reactome Pathways dataset.

Defective MMAA causes methylmalonic aciduria type cblA Gene Set

From Reactome Pathways

proteins participating in the Defective MMAA causes methylmalonic aciduria type cblA pathway from the Reactome Pathways dataset.

Defective CHSY1 causes TPBS Gene Set

From Reactome Pathways

proteins participating in the Defective CHSY1 causes TPBS pathway from the Reactome Pathways dataset.

Defective EXT2 causes exostoses 2 Gene Set

From Reactome Pathways

proteins participating in the Defective EXT2 causes exostoses 2 pathway from the Reactome Pathways dataset.

Defective B3GAT3 causes JDSSDHD Gene Set

From Reactome Pathways

proteins participating in the Defective B3GAT3 causes JDSSDHD pathway from the Reactome Pathways dataset.

Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF Gene Set

From Reactome Pathways

proteins participating in the Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF pathway from the Reactome Pathways dataset.

Defective ALG9 causes ALG9-CDG (CDG-1l) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG9 causes ALG9-CDG (CDG-1l) pathway from the Reactome Pathways dataset.

Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX) pathway from the Reactome Pathways dataset.

Defective MTR causes methylmalonic aciduria and homocystinuria type cblG Gene Set

From Reactome Pathways

proteins participating in the Defective MTR causes methylmalonic aciduria and homocystinuria type cblG pathway from the Reactome Pathways dataset.

Defective GGT1 causes Glutathionuria (GLUTH) Gene Set

From Reactome Pathways

proteins participating in the Defective GGT1 causes Glutathionuria (GLUTH) pathway from the Reactome Pathways dataset.

Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) pathway from the Reactome Pathways dataset.

Defective ALG1 causes ALG1-CDG (CDG-1k) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG1 causes ALG1-CDG (CDG-1k) pathway from the Reactome Pathways 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.

Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD Gene Set

From Reactome Pathways

proteins participating in the Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD pathway from the Reactome Pathways dataset.

Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD) Gene Set

From Reactome Pathways

proteins participating in the Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD) pathway from the Reactome Pathways dataset.

Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) pathway from the Reactome Pathways dataset.

Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD) Gene Set

From Reactome Pathways

proteins participating in the Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD) pathway from the Reactome Pathways dataset.

Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A) pathway from the Reactome Pathways dataset.

Defective EXT1 causes exostoses 1, TRPS2 and CHDS Gene Set

From Reactome Pathways

proteins participating in the Defective EXT1 causes exostoses 1, TRPS2 and CHDS pathway from the Reactome Pathways dataset.

Defective MPDU1 causes MPDU1-CDG (CDG-1f) Gene Set

From Reactome Pathways

proteins participating in the Defective MPDU1 causes MPDU1-CDG (CDG-1f) pathway from the Reactome Pathways dataset.

Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5) pathway from the Reactome Pathways dataset.

Defective CUBN causes hereditary megaloblastic anemia 1 Gene Set

From Reactome Pathways

proteins participating in the Defective CUBN causes hereditary megaloblastic anemia 1 pathway from the Reactome Pathways dataset.

Defects in vitamin and cofactor metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in vitamin and cofactor metabolism pathway from the Reactome Pathways dataset.

Defective GIF causes intrinsic factor deficiency Gene Set

From Reactome Pathways

proteins participating in the Defective GIF causes intrinsic factor deficiency pathway from the Reactome Pathways dataset.

Defective UGT1A4 causes hyperbilirubinemia Gene Set

From Reactome Pathways

proteins participating in the Defective UGT1A4 causes hyperbilirubinemia pathway from the Reactome Pathways dataset.

Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Gene Set

From Reactome Pathways

proteins participating in the Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) pathway from the Reactome Pathways dataset.

Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) pathway from the Reactome Pathways dataset.

Defective ALG11 causes ALG11-CDG (CDG-1p) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG11 causes ALG11-CDG (CDG-1p) pathway from the Reactome Pathways dataset.

Defective SLC26A2 causes chondrodysplasias Gene Set

From Reactome Pathways

proteins participating in the Defective SLC26A2 causes chondrodysplasias pathway from the Reactome Pathways dataset.

Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE Gene Set

From Reactome Pathways

proteins participating in the Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE pathway from the Reactome Pathways dataset.

Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR) pathway from the Reactome Pathways dataset.

Defective TCN2 causes hereditary megaloblastic anemia Gene Set

From Reactome Pathways

proteins participating in the Defective TCN2 causes hereditary megaloblastic anemia pathway from the Reactome Pathways dataset.

Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.

Defective MUT causes methylmalonic aciduria mut type Gene Set

From Reactome Pathways

proteins participating in the Defective MUT causes methylmalonic aciduria mut type pathway from the Reactome Pathways dataset.

Defective MAN1B1 causes MRT15 Gene Set

From Reactome Pathways

proteins participating in the Defective MAN1B1 causes MRT15 pathway from the Reactome Pathways dataset.

Defective CHST6 causes MCDC1 Gene Set

From Reactome Pathways

proteins participating in the Defective CHST6 causes MCDC1 pathway from the Reactome Pathways dataset.

Defective ALG2 causes ALG2-CDG (CDG-1i) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG2 causes ALG2-CDG (CDG-1i) pathway from the Reactome Pathways dataset.

Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) pathway from the Reactome Pathways dataset.

Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.

Defective CHST14 causes EDS, musculocontractural type Gene Set

From Reactome Pathways

proteins participating in the Defective CHST14 causes EDS, musculocontractural type pathway from the Reactome Pathways dataset.

Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD) Gene Set

From Reactome Pathways

proteins participating in the Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD) pathway from the Reactome Pathways dataset.

Defective CD320 causes methylmalonic aciduria Gene Set

From Reactome Pathways

proteins participating in the Defective CD320 causes methylmalonic aciduria pathway from the Reactome Pathways dataset.

Defects in biotin (Btn) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in biotin (Btn) metabolism pathway from the Reactome Pathways dataset.

Defective ACTH causes Obesity and Pro-opiomelanocortinin deficiency (POMCD) Gene Set

From Reactome Pathways

proteins participating in the Defective ACTH causes Obesity and Pro-opiomelanocortinin deficiency (POMCD) pathway from the Reactome Pathways dataset.

Defective ALG12 causes ALG12-CDG (CDG-1g) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG12 causes ALG12-CDG (CDG-1g) pathway from the Reactome Pathways dataset.

Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) pathway from the Reactome Pathways dataset.

Defective UGT1A1 causes hyperbilirubinemia Gene Set

From Reactome Pathways

proteins participating in the Defective UGT1A1 causes hyperbilirubinemia pathway from the Reactome Pathways dataset.

Defective ALG3 causes ALG3-CDG (CDG-1d) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG3 causes ALG3-CDG (CDG-1d) pathway from the Reactome Pathways dataset.

Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.

Defective CHST3 causes SEDCJD Gene Set

From Reactome Pathways

proteins participating in the Defective CHST3 causes SEDCJD pathway from the Reactome Pathways dataset.

Defective BTD causes biotidinase deficiency Gene Set

From Reactome Pathways

proteins participating in the Defective BTD causes biotidinase deficiency pathway from the Reactome Pathways dataset.

Defective B4GALT7 causes EDS, progeroid type Gene Set

From Reactome Pathways

proteins participating in the Defective B4GALT7 causes EDS, progeroid type pathway from the Reactome Pathways dataset.

Defective MOGS causes MOGS-CDG (CDG-2b) Gene Set

From Reactome Pathways

proteins participating in the Defective MOGS causes MOGS-CDG (CDG-2b) pathway from the Reactome Pathways dataset.

Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD) Gene Set

From Reactome Pathways

proteins participating in the Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD) pathway from the Reactome Pathways dataset.

Defective HLCS causes multiple carboxylase deficiency Gene Set

From Reactome Pathways

proteins participating in the Defective HLCS causes multiple carboxylase deficiency pathway from the Reactome Pathways dataset.

Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2 Gene Set

From Reactome Pathways

proteins participating in the Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2 pathway from the Reactome Pathways dataset.

Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4) pathway from the Reactome Pathways dataset.

Processing-defective Hh variants abrogate ligand secretion Gene Set

From Reactome Pathways

proteins participating in the Processing-defective Hh variants abrogate ligand secretion pathway from the Reactome Pathways dataset.