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  3. MYOZ2
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Molecular autopsy

Gene: MYOZ2

Red List (low evidence)
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: 0.86

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • 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

20 Feb 2019, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

Source London South GLH was added to MYOZ2.

20 Dec 2018, Gel status: 1

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

Ellen McDonagh (Genomics England Curator)

gene: MYOZ2 was added gene: MYOZ2 was added to Molecular autopsy. Sources: Expert Review Red 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,