Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol MYH6 contributors: mct - updated : 03-06-2014
HGNC name myosin, heavy chain 6, cardiac muscle, alpha
HGNC id 7576
ASSOCIATED DISORDERS
corresponding disease(s) CMH6 , ASD3 , SSS3 , CMD1EE
Susceptibility to variation of cardiac conduction
Variant & Polymorphism SNP
  • c.2161C>T missense mutation in MYH6 resulting in p.Arg721Trp associates with SSS3
  • common variants in this gene modulate cardiac conduction affecting heart rate and the PR intervall
  • Candidate gene
    Marker
    Therapy target
    SystemTypeDisorderPubmed
    cardiovascularaquiredheart failure
    activation of myosin by omecamtiv mecarbil may provide a new therapeutic approach for systolic heart failure
    ANIMAL & CELL MODELS