Genomics England
GMS Panels
Panels
Genes and Entities

KCND3

potassium voltage-gated channel subfamily D member 3
OMIM: 605411
PanelMode of inheritanceDetails
4 panels
Green
in Adult onset neurodegenerative disorder
R-numbers: R58
Signed-off version 4.41
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellarataxia19, OMIM:607346
Green
in Ataxia and cerebellar anomalies - narrow panel
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 4.40
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellarataxia19,607346
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
KCND3-related developmental disorder (monoallelic)
Green
in Hereditary ataxia with onset in adulthood
R-numbers: R54
Signed-off version 4.26
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellar ataxia 19, 607346, Spinocerebellarataxia19, 607346