This Panel is marked as Internal
Paediatric or syndromic cardiomyopathy - previous panel
Gene: MYH7
MYH7 (myosin heavy chain 7)
EnsemblGeneIds (GRCh38): ENSG00000092054
EnsemblGeneIds (GRCh37): ENSG00000092054
OMIM: 160760, Gene2Phenotype
MYH7 is in 14 panels
EnsemblGeneIds (GRCh38): ENSG00000092054
EnsemblGeneIds (GRCh37): ENSG00000092054
OMIM: 160760, Gene2Phenotype
MYH7 is in 14 panels
0 reviews
Details
- Mode of Inheritance
- BOTH monoallelic and biallelic, autosomal or pseudoautosomal
- Sources
-
- South West GLH
- OMIM
- 160760
- Clinvar variants
- Variants in MYH7
- Penetrance
- None
- Panels with this gene
-
- Paediatric or syndromic cardiomyopathy
- Paediatric disorders - additional genes
- Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies
- Left Ventricular Noncompaction Cardiomyopathy
- Hereditary neuropathy or pain disorder
- Congenital myopathy
- Hypertrophic cardiomyopathy
- Dilated Cardiomyopathy and conduction defects
- Fetal anomalies
- Hereditary neuropathy
- Fetal hydrops
- Distal myopathies
- Arthrogryposis
- Dilated and arrhythmogenic cardiomyopathy
History Filter Activity
21 Feb 2019, Gel status: 1
Created, Added New Source, Set mode of inheritance
Ellen McDonagh (Genomics England Curator)gene: MYH7 was added gene: MYH7 was added to Paediatric or syndromic cardiomyopathy. Sources: South West GLH Mode of inheritance for gene: MYH7 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal