Sudden death in young people

Gene: CTNNA3

No list

CTNNA3 (catenin alpha 3)
EnsemblGeneIds (GRCh38): ENSG00000183230
EnsemblGeneIds (GRCh37): ENSG00000183230
OMIM: 607667, Gene2Phenotype
CTNNA3 is in 3 panels

1 review

Rebecca Foulger (Genomics England curator)

Comment on list classification: Changed rating from red to grey: CTNNA3 is red on the V1.1 Arrhythmogenic Right Ventricular Cardiomyopathy panel.
Created: 6 Dec 2016, 4:35 p.m.

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Removed
  • Other
  • Emory Genetics Laboratory
Phenotypes
  • Arrhythmias
  • Arrhythmogenic right ventricular dysplasia, familial, 13, 615616
OMIM
607667
Clinvar variants
Variants in CTNNA3
Penetrance
Complete
Panels with this gene

History Filter Activity

19 Dec 2016, Gel status: 0

panel promoted to version 1

Ellen Thomas (Genomics England Curator)

This panel contains genes which aren't arrhythmic or metabolic causes of sudden death with normal post mortem.

6 Dec 2016, Gel status: 0

Gene classified by Genomics England curator

Rebecca Foulger (Genomics England curator)

This gene has been removed from the panel.

6 Dec 2016, Gel status: 1

Set Mode of Inheritance, Added New Source

Rebecca Foulger (Genomics England curator)

CTNNA3 was added to Sudden death in young peoplepanel. Source: Other Model of inheritance for gene CTNNA3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

6 Dec 2016, Gel status: 1

Added New Source

Rebecca Foulger (Genomics England curator)

CTNNA3 was added to Sudden death in young peoplepanel. Sources: Emory Genetics Laboratory

6 Dec 2016, Gel status: 0

Created

Rebecca Foulger (Genomics England curator)

CTNNA3 was created by rfoulger