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  3. KCNJ8
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Cardiac arrhythmias - previous panel

Gene: KCNJ8

Red List (low evidence)
KCNJ8 (potassium voltage-gated channel subfamily J member 8)
EnsemblGeneIds (GRCh38): ENSG00000121361
EnsemblGeneIds (GRCh37): ENSG00000121361
OMIM: 600935, Gene2Phenotype
KCNJ8 is in 6 panels

0 reviews

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
Phenotypes
  • Brugada/Brugada like syndrome
  • short qt
  • ventricular tachycardia
  • atrial fibrillation
OMIM
600935
Clinvar variants
Variants in KCNJ8
Penetrance
None
Publications
Mode of Pathogenicity
Other
Panels with this gene

History Filter Activity

28 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Ellen McDonagh (Genomics England Curator)

Eleanor Williams: Sources: Literature

20 Dec 2018, Gel status: 1

Set mode of pathogenicity

Rebecca Foulger (Genomics England curator)

Mode of pathogenicity for gene: KCNJ8 was changed from to Other

17 Dec 2018, Gel status: 1

Set Phenotypes

Rebecca Foulger (Genomics England curator)

Added phenotypes atrial fibrillation; ventricular tachycardia; short qt for gene: KCNJ8

17 Dec 2018, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Rebecca Foulger (Genomics England curator)

gene: KCNJ8 was added gene: KCNJ8 was added to Cardiac arrythmias. Sources: Expert Review Red Mode of inheritance for gene: KCNJ8 was set to Unknown Publications for gene: KCNJ8 were set to 21383000; 15569843; 27283775 Phenotypes for gene: KCNJ8 were set to Brugada/Brugada like syndrome