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 Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure. 21750094 2011
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 Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation. 20031619 2009
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy. 24664454 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathy. 21211974 2011
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 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 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 Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy. 24119082 2013
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 GeneticVariation group CLINVAR Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians. 25448463 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 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 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 GeneticVariation group CLINVAR Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257 2017
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 CausalMutation group CLINVAR Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure. 21750094 2011
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy. 15556047 2004
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR Prognostic Relevance of Gene-Environment Interactions in Patients With Dilated Cardiomyopathy: Applying the MOGE(S) Classification. 26383716 2015
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 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 Genetic Testing in Pediatric Left Ventricular Noncompaction. 29212898 2017
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.490 GeneticVariation group CLINVAR The sarcomeric M-region: a molecular command center for diverse cellular processes. 25961035 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 Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy. 24664454 2014
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 Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257 2017