KEGG   VARIANT: 4625v1
Entry
4625v1                      Variant                                
Name
MYH7 mutation
Type
Loss of function
Gene
MYH7  myosin-7 [KO:K17751]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 160760
Network
nt06539  Cytoskeleton in muscle cells
Disease
H00292  Hypertrophic cardiomyopathy
H00294  Dilated cardiomyopathy
H00594  Distal myopathy
H01810  Congenital myopathy
Reference
PMID:37079208
  Authors
Gao Y, Peng L, Zhao C
  Title
MYH7 in cardiomyopathy and skeletal muscle myopathy.
  Journal
Mol Cell Biochem 479:393-417 (2024)
DOI:10.1007/s11010-023-04735-x
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