CTNNA3

catenin alpha 3
OMIM: 607667, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber CTNNA3 in Arrhythmogenic Cardiomyopathy


Level 2: Cardiovascular disorders
Version 0.74

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Arrhythmia_SuperPanel
  • Cardiomyopathy_Adult_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Other
    Phenotypes
    • Arrhythmogenic right ventricular cardiomyopathy
    • Arrhythmogenic right ventricular dysplasia, familial, 13 MIM#615616

    Red CTNNA3 in Congenital Heart Defect


    Level 2: Cardiovascular disorders
    Version 0.511

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • ClinGen
    Phenotypes
    • Congenital heart disease, MONDO:0005453
    Tags
    • disputed

    Amber CTNNA3 in Mendeliome


    Version 1.3795

    2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • ClinGen
    • Expert Review Amber
    • ClinGen
    Phenotypes
    • Arrhythmogenic right ventricular cardiomyopathy
    • Arrhythmogenic right ventricular dysplasia, familial, 13 MIM#615616