GJA5

gap junction protein alpha 5
OMIM: 121013, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red GJA5 in Progressive cardiac conduction disease


Version 2.8
Latest signed off version: v2.7 (1 May 2024)

Component of the following Super Panels:

  • Sudden unexplained death or survivors of a cardiac event
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • South West GLH
    Phenotypes
    • Heart conduction disease, MONDO:0000992