Gene: MYH7 ×
Source: CLINVAR ×
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 A new missense mutation, Arg719Gln, in the beta-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy. 7848441 1994
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians. 25448463 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure. 10065021 1998
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden. 12818575 2003
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR A transgenic rabbit model for human hypertrophic cardiomyopathy. 10606622 1999
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Utility of genetic screening in hypertrophic cardiomyopathy: prevalence and significance of novel and double (homozygous and heterozygous) beta-myosin mutations. 12820698 2003
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Mutation of Arg723Gly in beta-myosin heavy chain gene in five Chinese families with hypertrophic cardiomyopathy. 17097032 2006
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Genetics of hypertrophic cardiomyopathy in Norway. 24111713 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR [Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy]. 17125710 2006
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Multidimensional structure-function relationships in human β-cardiac myosin from population-scale genetic variation. 27247418 2016
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy. 7883988 1995
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR [Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy]. 17125710 2006
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation. 20031619 2009
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Prevalence and distribution of sarcomeric gene mutations in Japanese patients with familial hypertrophic cardiomyopathy. 22112859 2012
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy. 21310275 2011
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Good Intentions Gone Bad. 31112422 2019
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β. 20811150 2010
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 GeneticVariation disease CLINVAR Echocardiographic strain imaging to assess early and late consequences of sarcomere mutations in hypertrophic cardiomyopathy. 20031602 2009
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 CausalMutation disease CLINVAR Microvascular function is selectively impaired in patients with hypertrophic cardiomyopathy and sarcomere myofilament gene mutations. 21835320 2011
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family. 9874056 1998
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy. 21302287 2011
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Gene-specific increase in the energetic cost of contraction in hypertrophic cardiomyopathy caused by thick filament mutations. 24835277 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Characterization of mutant myosins of Dictyostelium discoideum equivalent to human familial hypertrophic cardiomyopathy mutants. Molecular force level of mutant myosins may have a prognostic implication. 9062359 1997