Genomics England
GMS Panels
Panels
Genes and Entities

KCNC3

potassium voltage-gated channel subfamily C member 3
OMIM: 176264
PanelMode of inheritanceDetails
5 panels
Green
in Adult onset neurodegenerative disorder
R-numbers: R58
Signed-off version 7.10
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Spinocerebellar ataxia 13, OMIM:605259
Green
in Ataxia and cerebellar anomalies - narrow panel
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 7.19
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellar ataxia 13
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.48
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
SPINOCEREBELLAR ATAXIA TYPE 13 605259
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 5.80
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellar ataxia 13, OMIM:605259
Green
in Hereditary ataxia with onset in adulthood
R-numbers: R54
Signed-off version 7.11
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Spinocerebellar ataxia 13, 605259, Spinocerebellar ataxia 13