Genomics England
GMS Panels
Panels
Genes and Entities

VPS13D

vacuolar protein sorting 13 homolog D
OMIM: 608877
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
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spinocerebellar ataxia, autosomal recessive 4, 607317
Green
in Childhood onset dystonia, chorea or related movement disorder
R-numbers: R57
Signed-off version 5.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spinocerebellar ataxia, autosomal recessive 4, 607317
Green
in Hereditary ataxia with onset in adulthood
R-numbers: R54
Signed-off version 6.7
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Autosomal recessive spinocerebellar ataxia 4, 608877, Spinocerebellar ataxia, autosomal recessive 4, 607317