This Panel is marked as Internal
Cardiac arrhythmias - previous panel
Gene: KCND3
KCND3 (potassium voltage-gated channel subfamily D member 3)
EnsemblGeneIds (GRCh38): ENSG00000171385
EnsemblGeneIds (GRCh37): ENSG00000171385
OMIM: 605411, Gene2Phenotype
KCND3 is in 11 panels
EnsemblGeneIds (GRCh38): ENSG00000171385
EnsemblGeneIds (GRCh37): ENSG00000171385
OMIM: 605411, Gene2Phenotype
KCND3 is in 11 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- Phenotypes
-
- Brugada/Brugada like syndrome
- OMIM
- 605411
- Clinvar variants
- Variants in KCND3
- Penetrance
- None
- Panels with this gene
-
- Hereditary ataxia with onset in adulthood
- Adult onset neurodegenerative disorder
- Intellectual disability
- DDG2P
- Ataxia and cerebellar anomalies - narrow panel
- Childhood onset dystonia, chorea or related movement disorder
- Hereditary ataxia
- Short QT syndrome
- Early onset or syndromic epilepsy
- Brugada syndrome and cardiac sodium channel disease
- Sudden death in young people
History Filter Activity
28 Jan 2019, Gel status: 1
Panel promoted to version 1.0
Ellen McDonagh (Genomics England Curator)Eleanor Williams: Sources: Literature
17 Dec 2018, Gel status: 1
Set Phenotypes
Rebecca Foulger (Genomics England curator)Added phenotypes Brugada/Brugada like syndrome for gene: KCND3
17 Dec 2018, Gel status: 1
Created, Added New Source, Set mode of inheritance
Rebecca Foulger (Genomics England curator)gene: KCND3 was added gene: KCND3 was added to Cardiac arrythmias. Sources: Expert Review Red Mode of inheritance for gene: KCND3 was set to Unknown