Genomics England
GMS Panels
Panels
Genes and Entities

RNF170

ring finger protein 170
OMIM: 614649
PanelMode of inheritanceDetails
3 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 6.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Ataxia, sensory, 1, autosomal dominant
Green
in Childhood onset hereditary spastic paraplegia
R-numbers: R61
Signed-off version 6.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic paraplegia 85, autosomal recessive, OMIM:619686
Green
in Hereditary ataxia with onset in adulthood
R-numbers: R54
Signed-off version 6.7
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Autosomal dominant sensory ataxia 1, 608984, Ataxia, sensory, 1, autosomal dominant