Genomics England

ATXN2_CAG

ataxin 2

Panel	Mode of inheritance	Details
Filter panels7 panels
Green in Ataxia and cerebellar anomalies - childhood onset Component of the following Super Panels: - Hereditary ataxia and cerebellar anomalies, childhood onset Signed-off version 9.22	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 2, OMIM:183090
Green in Dystonia, chorea or related movement disorder, adult onset Component of the following Super Panels: - Adult-onset neurological disorders Signed-off version 6.7	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 2, OMIM:183090, {Amyotrophic lateral sclerosis, susceptibility to, 13}, OMIM:183090, {Parkinson disease, late-onset, susceptibility to}, OMIM:168600
Green in Dystonia, chorea or related movement disorder, childhood onset R-numbers: R57 Signed-off version 8.13	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 2, OMIM:183090, {Amyotrophic lateral sclerosis, susceptibility to, 13}, OMIM:183090
Green in Hereditary ataxia, adult onset Component of the following Super Panels: - Adult-onset neurological disorders Signed-off version 9.4	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 2, OMIM:183090
Green in Hereditary neuropathy or pain disorder R-numbers: R78 Signed-off version 8.30	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 2, OMIM:183090
Green in Hereditary spastic paraplegia, adult onset Component of the following Super Panels: - Adult-onset neurological disorders Signed-off version 6.13	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 2, OMIM:183090, {Amyotrophic lateral sclerosis, susceptibility to, 13}, OMIM:183090
Green in Neurodegenerative disorders, adult onset Component of the following Super Panels: - Adult-onset neurological disorders Signed-off version 9.4	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 2, OMIM:183090, {Amyotrophic lateral sclerosis, susceptibility to, 13}, OMIM:183090, {Parkinson disease, late-onset, susceptibility to}, OMIM:168600