Sudden death in young people
Gene: CTNNA3EnsemblGeneIds (GRCh38): ENSG00000183230
EnsemblGeneIds (GRCh37): ENSG00000183230
OMIM: 607667, Gene2Phenotype
CTNNA3 is in 2 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
- Tags
- OMIM
- 607667
- Clinvar variants
- Variants in CTNNA3
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
Added Tag
Arina Puzriakova (Genomics England Curator)Tag curated_removed tag was added to gene: CTNNA3.
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.
Gene classified by Genomics England curator
Rebecca Foulger (Genomics England curator)This gene has been removed from the panel.
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
Added New Source
Rebecca Foulger (Genomics England curator)CTNNA3 was added to Sudden death in young peoplepanel. Sources: Emory Genetics Laboratory
Created
Rebecca Foulger (Genomics England curator)CTNNA3 was created by rfoulger