Sudden cardiac death - previous panel
Gene: KCND3EnsemblGeneIds (GRCh38): ENSG00000171385
EnsemblGeneIds (GRCh37): ENSG00000171385
OMIM: 605411, Gene2Phenotype
KCND3 is in 11 panels
1 review
Ellen McDonagh (Genomics England Curator)
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.
Details
- Mode of Inheritance
- Unknown
- Sources
-
- London South GLH
- Expert Review Red
- London South GLH
- Expert Review Red
- Phenotypes
-
- sudden unexplained death
- arrhythmia
- Brugada/Brugada like syndrome
- sudden cardiac arrest
- OMIM
- 605411
- Clinvar variants
- Variants in KCND3
- Penetrance
- None
- Publications
- Panels with this gene
-
- Hereditary ataxia with onset in adulthood
- Childhood onset dystonia, chorea or related movement disorder
- Short QT syndrome
- Brugada syndrome and cardiac sodium channel disease
- Adult onset neurodegenerative disorder
- Intellectual disability
- Hereditary ataxia
- DDG2P
- Ataxia and cerebellar anomalies - narrow panel
- Early onset or syndromic epilepsy
- Sudden death in young people
History Filter Activity
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Ivone Leong (Genomics England Curator)gene: KCND3 was added gene: KCND3 was added to Sudden cardiac death. Sources: Expert Review Red,London South GLH Mode of inheritance for gene: KCND3 was set to Unknown Publications for gene: KCND3 were set to 22457051 Phenotypes for gene: KCND3 were set to sudden unexplained death; arrhythmia; Brugada/Brugada like syndrome; sudden cardiac arrest