Genomics England
GMS Panels
Panels
Genes and Entities

MAG

myelin associated glycoprotein
OMIM: 159460
PanelMode of inheritanceDetails
4 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 7.19
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic paraplegia 75, autosomal recessive, OMIM:616680
Green
in Childhood onset hereditary spastic paraplegia
R-numbers: R61
Signed-off version 7.7
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic paraplegia 75, autosomal recessive, OMIM:616680
Green
in Hereditary neuropathy or pain disorder
R-numbers: R78
Signed-off version 6.163
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic paraplegia 75, autosomal recessive, OMIM:616680
Green
in Optic neuropathy
R-numbers: R41
Signed-off version 4.40
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic paraplegia 75, autosomal recessive, OMIM:616680