Sudden cardiac death - previous panel
Gene: KCNJ5
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.
Gene currently tested on Manchester cardiac gene panel. 16 variants listed on HGMD (accessed 29/01/2019). ClinGen Knowledge Base: gene not curated (accessed 29/01/2019).Created: 14 Feb 2019, 1:38 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Long QT syndrome 13 (613485); Hyperaldosteronism, familial, type III (613677)
Publications
Variants in this GENE are reported as part of current diagnostic practice
gene: KCNJ5 was added gene: KCNJ5 was added to Sudden cardiac death. Sources: Expert Review Green,North West GLH,London South GLH Mode of inheritance for gene: KCNJ5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: KCNJ5 were set to 19862833; 19716085; 16301704; 30420954 Phenotypes for gene: KCNJ5 were set to Long QT syndrome 13 (613485); Long QT syndrome 13; Hyperaldosteronism, familial, type III (613677)