Gene: MYPN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84665
Gene Symbol: MYPN
MYPN 		0.430 GeneticVariation group BEFREE Autosomal recessive MYPN mutations have been reported in only six families showing a mildly progressive nemaline or cap myopathy with cardiomyopathy in some patients. 31133047 2019
Entrez Id: 84665
Gene Symbol: MYPN
MYPN 		0.430 GeneticVariation group BEFREE Dominant MYPN mutations were previously reported in cardiomyopathies. 28220527 2017
Entrez Id: 84665
Gene Symbol: MYPN
MYPN 		0.430 GeneticVariation group BEFREE Two nonsense and 13 missense MYPN variants were identified in subjects with DCM, HCM and RCM with the average cardiomyopathy prevalence of 1.66%. 22286171 2012
Entrez Id: 84665
Gene Symbol: MYPN
MYPN 		0.430 Biomarker group GENOMICS_ENGLAND
Entrez Id: 84665
Gene Symbol: MYPN
MYPN 		0.430 Biomarker group HPO