Genomics England
GMS Panels
Panels
Genes and Entities

MYH6

myosin heavy chain 6
OMIM: 160710
PanelMode of inheritanceDetails
2 panels
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
ATRIAL SEPTAL DEFECT TYPE 3, CARDIOMYOPATHY DILATED TYPE 1EE, CARDIOMYOPATHY FAMILIAL HYPERTROPHIC TYPE 14
Green
in Paediatric or syndromic cardiomyopathy
Component of the following Super Panels:
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R135
Signed-off version 4.3
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Atrial septal defect 3, OMIM:614089, Cardiomyopathy, dilated, 1EE OMIM:613252, Cardiomyopathy, hypertrophic, 14, OMIM:613251, {Sick sinus syndrome 3}, OMIM:614090