Sudden cardiac death - previous panel
Gene: DTNA

DTNA (dystrobrevin alpha)
EnsemblGeneIds (GRCh38): ENSG00000134769
EnsemblGeneIds (GRCh37): ENSG00000134769
OMIM: 601239, Gene2Phenotype
DTNA is in 7 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

Left ventricular noncompaction 1, with or without congenital heart defects,

OMIM

601239

Clinvar variants

Variants in DTNA

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: DTNA was added gene: DTNA was added to Sudden cardiac death. Sources: Expert Review Red,London South GLH Mode of inheritance for gene: DTNA was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: DTNA were set to Left ventricular noncompaction 1, with or without congenital heart defects,

Sudden cardiac death - previous panel Gene: DTNA