Sudden cardiac death - previous panel
Gene: MYOZ2

MYOZ2 (myozenin 2)
EnsemblGeneIds (GRCh38): ENSG00000172399
EnsemblGeneIds (GRCh37): ENSG00000172399
OMIM: 605602, Gene2Phenotype
MYOZ2 is in 3 panels

1 review

Ellen McDonagh (Genomics England Curator)

I don't know

This gene was part of an initial gene list collated by Matthew Edwards Royal Brompton Hospital sent 16th Jan 2019 on behalf of the London South GLH for review by the GMS Cardiology Specialist Group. Only gene symbol from the Royal Brompton gene panel was provided - suggested initial gene rating and evidence for inclusion not provided with the list.
Created: 20 Feb 2019, 2:17 p.m.

Created: 20 Feb 2019, 2:17 p.m.

Panel version: Imported from Molecular autopsy panel version 0.86

Details

Mode of Inheritance

MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Sources

London South GLH
Expert Review Red
London South GLH
Expert Review Red

Phenotypes

Cardiomyopathy, familial hypertrophic, 16,

OMIM

605602

Clinvar variants

Variants in MYOZ2

Penetrance

None

Panels with this gene

History Filter Activity

9 Sep 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ivone Leong (Genomics England Curator)

gene: MYOZ2 was added gene: MYOZ2 was added to Sudden cardiac death. Sources: Expert Review Red,London South GLH Mode of inheritance for gene: MYOZ2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: MYOZ2 were set to Cardiomyopathy, familial hypertrophic, 16,

Sudden cardiac death - previous panel Gene: MYOZ2