Sudden death in young people
Gene: KCNJ8EnsemblGeneIds (GRCh38): ENSG00000121361
EnsemblGeneIds (GRCh37): ENSG00000121361
OMIM: 600935, Gene2Phenotype
KCNJ8 is in 6 panels
2 reviews
Ellen Thomas (Genomics England Curator)
Comment on list classification: Paper suggesting mutations predispose to SIDS; only 2 cases, one variant missense, no inheritance studies. Await further evidence.Created: 19 Dec 2016, 3:42 p.m.
Rebecca Foulger (Genomics England curator)
Note that KCNJ8 is a red gene on the Brugada panel, but is included on this 'Sudden death in young people' panel because of the 'sudden infant death syndrome' phenotypes iin Radboud.Created: 6 Dec 2016, 2:42 p.m.
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Amber
- Radboud University Medical Center, Nijmegen
- Emory Genetics Laboratory
- Phenotypes
-
- arrhythmia
- Sudden infant death syndrome
- ?Ventricular fibrillation
- OMIM
- 600935
- Clinvar variants
- Variants in KCNJ8
- Penetrance
- Complete
- Publications
-
- PMID: 21836131
- Panels with this gene
History Filter Activity
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
Ellen Thomas (Genomics England Curator)This gene has been classified as Amber List (Moderate Evidence).
Set publications
Ellen Thomas (Genomics England Curator)Publications for KCNJ8 were set to PMID: 21836131
Added New Source
Rebecca Foulger (Genomics England curator)KCNJ8 was added to Sudden death in young peoplepanel. Source: Radboud University Medical Center, Nijmegen
Added New Source
Rebecca Foulger (Genomics England curator)KCNJ8 was added to Sudden death in young peoplepanel. Sources: Emory Genetics Laboratory
Created
Rebecca Foulger (Genomics England curator)KCNJ8 was created by rfoulger