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 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 Genetic Testing in Pediatric Left Ventricular Noncompaction. 29212898 2017
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
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 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 The sarcomeric M-region: a molecular command center for diverse cellular processes. 25961035 2015
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 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 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 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 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 CausalMutation group CLINVAR The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing. 24503780 2014
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 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 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 CausalMutation group CLINVAR Myosinopathies: pathology and mechanisms. 22918376 2013
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 Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy families. 23054336 2013
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 Genetic testing for dilated cardiomyopathy in clinical practice. 22464770 2012
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 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 Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathy. 22949430 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 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