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 		0.490 GeneticVariation group CLINVAR 165th ENMC International Workshop: distal myopathies 6-8th February 2009 Naarden, The Netherlands. 19477645 2009
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR 165th ENMC International Workshop: distal myopathies 6-8th February 2009 Naarden, The Netherlands. 19477645 2009
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR A de novo germline mutation in MYH7 causes a progressive dominant myopathy in pigs. 23153285 2012
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR A low prevalence of sarcomeric gene variants in a Chinese cohort with left ventricular non-compaction. 24691700 2015
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR A rare mutation in MYH7 gene occurs with overlapping phenotype. 25576864 2015
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy. 18660445 2008
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function. 16983074 2006
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group 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 		0.490 GeneticVariation group CLINVAR Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy. 19412328 2008
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy. 19412328 2008
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR Effects of pathogenic proline mutations on myosin assembly. 22155079 2012
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR Electrocardiographic features of sarcomere mutation carriers with and without clinically overt hypertrophic cardiomyopathy. 21943931 2011
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group 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 		0.490 GeneticVariation group CLINVAR Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era. 22337857 2012
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group 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 		0.490 CausalMutation group CLINVAR Genetic testing for dilated cardiomyopathy in clinical practice. 22464770 2012
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR Genetic testing for dilated cardiomyopathy in clinical practice. 22464770 2012
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR Genetic Testing in Pediatric Left Ventricular Noncompaction. 29212898 2017
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR Haplotype sharing test maps genes for familial cardiomyopathies. 20573160 2011
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR Human growth hormone stimulates somatomedin C/insulin-like growth factor I production by the human lymphoid cell line, IM-9. 2753225 1989
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse alpha-cardiac myosin in the laser trap assay. 17351073 2007
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR Loss of Function Mutations in NNT Are Associated With Left Ventricular Noncompaction. 26025024 2015
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene. 15769782 2005
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes. 19854198 2010
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. 11106718 2000