Gene: MYH7 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience. 23349452 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Creatine kinase adenosine triphosphate and phosphocreatine energy supply in a single kindred of patients with hypertrophic cardiomyopathy. 23751935 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Penetrance of hypertrophic cardiomyopathy in children and adolescents: a 12-year follow-up study of clinical screening and predictive genetic testing. 23197161 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Detection of a large duplication mutation in the myosin-binding protein C3 gene in a case of hypertrophic cardiomyopathy. 23816408 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Comparison of echocardiographic and cardiac magnetic resonance imaging in hypertrophic cardiomyopathy sarcomere mutation carriers without left ventricular hypertrophy. 23690394 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnostics. 23785128 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy. 23283745 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR T1 measurements identify extracellular volume expansion in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophy. 23549607 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy. 24093860 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing. 23396983 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Molecular consequences of the R453C hypertrophic cardiomyopathy mutation on human β-cardiac myosin motor function. 23798412 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Elevated rates of force development and MgATP binding in F764L and S532P myosin mutations causing dilated cardiomyopathy. 23313350 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy families. 23054336 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease BEFREE Cardiac samples from patients with HCM harboring mutations in genes encoding thick (MYH7, MYBPC3) and thin (TNNT2, TNNI3, TPM1) filament proteins were compared with sarcomere mutation-negative HCM and nonfailing donors. 23508784 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Penetrance of hypertrophic cardiomyopathy in children and adolescents: a 12-year follow-up study of clinical screening and predictive genetic testing. 23197161 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy. 23782526 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy. 23782526 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Cardiomyopathy mutations in the tail of β-cardiac myosin modify the coiled-coil structure and affect integration into thick filaments in muscle sarcomeres in adult cardiomyocytes. 24047955 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 Biomarker disease CTD_human Contractile abnormalities and altered drug response in engineered heart tissue from Mybpc3-targeted knock-in mice. 23896226 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy. 23711808 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy. 24119082 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells. 23290139 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy. 23283745 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathy. 23674513 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy. 23711808 2013