Cardiac arrhythmias - previous panel
Gene: KCNJ2EnsemblGeneIds (GRCh38): ENSG00000123700
EnsemblGeneIds (GRCh37): ENSG00000123700
OMIM: 600681, Gene2Phenotype
KCNJ2 is in 10 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Phenotypes
-
- LONG QT SYNDROME 7 (170390)
- ventricular tacyarrhythmia
- Short QT syndrome 3 609622
- short qt
- catecholaminergic polymorphic ventricular tachycardia
- ANDERSEN SYNDROME (170390)
- atrial fibrillation
- OMIM
- 600681
- Clinvar variants
- Variants in KCNJ2
- Penetrance
- None
- Publications
- Mode of Pathogenicity
- Other - please provide details in the comments
- Panels with this gene
History Filter Activity
Panel promoted to version 1.0
Ellen McDonagh (Genomics England Curator)Checked against the component panels, and ready to be promoted to version 1.
Set Phenotypes
Rebecca Foulger (Genomics England curator)Added phenotypes catecholaminergic polymorphic ventricular tachycardia for gene: KCNJ2
Set Phenotypes
Rebecca Foulger (Genomics England curator)Added phenotypes ANDERSEN SYNDROME (170390); LONG QT SYNDROME 7 (170390) for gene: KCNJ2
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes, Set mode of pathogenicity
Rebecca Foulger (Genomics England curator)gene: KCNJ2 was added gene: KCNJ2 was added to Cardiac arrythmias. Sources: Expert Review Green Mode of inheritance for gene: KCNJ2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: KCNJ2 were set to 23440193; 12163457; 15761194; 22308236; 24794859; 19710529; 22311718; 22155372; 25691870; 19285083 Phenotypes for gene: KCNJ2 were set to atrial fibrillation; Short QT syndrome 3 609622; ventricular tacyarrhythmia; short qt Mode of pathogenicity for gene: KCNJ2 was set to Other - please provide details in the comments