Genomics England

myelin associated glycoprotein

Panel	Mode of inheritance	Details
Filter panels5 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 9.0	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 9.0	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 8.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 75, autosomal recessive, OMIM:616680
Green in Intellectual disability Component of the following Super Panels: - Childhood onset leukodystrophy - Hypotonic infant - Paediatric disorders R-numbers: R29 Signed-off version 10.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 75, autosomal recessive, OMIM:616680, hereditary spastic paraplegia 75, MONDO:0014729
Green in Optic neuropathy R-numbers: R41 Signed-off version 6.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 75, autosomal recessive, OMIM:616680