Genomics England

solute carrier family 1 member 3

Panel	Mode of inheritance	Details
Filter panels4 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 2.23	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Episodic ataxia, type 6,
Green in Hereditary ataxia - adult onset R-numbers: R54 Signed-off version 2.13	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Episodic ataxia, type 6, Episodic ataxia type 6, 612656
Green in Paroxysmal central nervous system disorders R-numbers: R66 Signed-off version 1.2	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Episodic ataxia, type 6, 612656
Green in Skeletal muscle channelopathy R-numbers: R76 Signed-off version 1.2	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Episodic ataxia, type 6, 612656