Cardiac arrhythmias - previous panel
Gene: KCNE3EnsemblGeneIds (GRCh38): ENSG00000175538
EnsemblGeneIds (GRCh37): ENSG00000175538
OMIM: 604433, Gene2Phenotype
KCNE3 is in 4 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Phenotypes
-
- Brugada syndrome
- Brugada syndrome 6
- Long QT syndrome
- OMIM
- 604433
- Clinvar variants
- Variants in KCNE3
- Penetrance
- None
- Publications
-
- 19306396
- doi:10. 1007/ s12265-016-9673-5
- 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 Brugada syndrome; Long QT syndrome for gene: KCNE3
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Rebecca Foulger (Genomics England curator)gene: KCNE3 was added gene: KCNE3 was added to Cardiac arrythmias. Sources: Expert Review Green Mode of inheritance for gene: KCNE3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: KCNE3 were set to 19306396; doi:10. 1007/ s12265-016-9673-5 Phenotypes for gene: KCNE3 were set to Brugada syndrome 6