Genomics England
GMS Panels
Panels
Genes and Entities

CLCN2

chloride voltage-gated channel 2
OMIM: 600570
PanelMode of inheritanceDetails
5 panels
Green
in Ataxia and cerebellar anomalies - narrow panel
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 3.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Leukoencephalopathy with ataxia, OMIM:615651
Green
in Hereditary ataxia - adult onset
R-numbers: R54
Signed-off version 3.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Leukoencephalopathy with ataxia, OMIM:615651
Green
in Neurodegenerative disorders - adult onset
R-numbers: R58
Signed-off version 3.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Leukoencephalopathy with ataxia, OMIM:615651
Green
in White matter disorders - adult onset
R-numbers: R62
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Leukoencephalopathy with ataxia, OMIM:615651
Green
in White matter disorders and cerebral calcification - narrow panel
Component of the following Super Panels:
  • - White matter disorders - childhood onset
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Leukoencephalopathy with ataxia, OMIM:615651