1. Genes and Genomic Entities
  2. ATXN7

ATXN7

ataxin 7
OMIM: 607640, Gene2Phenotype

21 panels

Panel Reviews Mode of inheritance Details
21 panels
Red ATXN7 in Ataxia and cerebellar anomalies - narrow panel


Level 2: Neurology
Version 8.63
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Hereditary ataxia and cerebellar anomalies - childhood onset

    		•  review Other
    Sources
    • Expert Review Red
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • nucleotide-repeat-expansion
    • currently-ngs-unreportable
    Red ATXN7 in Hereditary ataxia

    Level 3: Motor Disorders of the CNS
    Level 2: Neurology and neurodevelopmental disorders
    Version 1.344

    		review Other
    Sources
    • Expert Review Red
    • Eligibility statement prior genetic testing
    • Radboud University Medical Center, Nijmegen
    • UKGTN
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • currently-ngs-unreportable
    • nucleotide-repeat-expansion
    Red ATXN7 in Adult onset neurodegenerative disorder


    Level 2: Neurology
    Version 8.11
    Latest signed off version: v8.0 (30 Apr 2025)

    		review Other
    Sources
    • Yorkshire and North East GLH
    • Expert Review Red
    • London North GLH
    • NHS GMS
    • South West GLH
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • nucleotide-repeat-expansion
    • currently-ngs-unreportable
    Red ATXN7 in Undiagnosed metabolic disorders

    Level 3: Specific metabolic abnormalities
    Level 2: Metabolic disorders
    Version 1.642

    		review Other
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • nucleotide-repeat-expansion
    • currently-ngs-unreportable
    Red ATXN7 in Likely inborn error of metabolism


    Level 2: Metabolic
    Version 8.91
    Latest signed off version: v8.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review Other
    Sources
    • London North GLH
    • NHS GMS
    • Expert Review Red
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    • Mitochondrial respiratory chain disorders (caused by nuclear variants only)
    Tags
    • nucleotide-repeat-expansion
    • currently-ngs-unreportable
    Red ATXN7 in Intellectual disability


    Level 2: Developmental disorders
    Version 9.285
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review Other
    Sources
    • Expert Review Red
    • Other
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • currently-ngs-unreportable
    • nucleotide-repeat-expansion
    Red ATXN7 in Hereditary ataxia with onset in adulthood


    Level 2: Neurology
    Version 8.23
    Latest signed off version: v8.0 (30 Apr 2025)

    		review Other
    Sources
    • NHS GMS
    • Wessex and West Midlands GLH
    • Expert Review Red
    • Hereditary ataxia v1.148
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • nucleotide-repeat-expansion
    • currently-ngs-unreportable
    Red ATXN7 in Retinal disorders


    Level 2: Ophthalmology
    Version 8.86
    Latest signed off version: v8.0 (30 Apr 2025)

    		review Other
    Sources
    • Expert Review Red
    • NHS GMS
    • RetNet
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • nucleotide-repeat-expansion
    • currently-ngs-unreportable
    Red ATXN7 in Childhood onset dystonia, chorea or related movement disorder


    Level 2: Neurology
    Version 7.13
    Latest signed off version: v7.0 (30 Apr 2025)

    		review Other
    Sources
    • Expert Review Red
    • London North GLH
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • nucleotide-repeat-expansion
    • currently-ngs-unreportable
    Green ATXN7_CAG STR in Ataxia and cerebellar anomalies - narrow panel


    Level 2: Neurology
    Version 8.63
    Latest signed off version: v8.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Hereditary ataxia and cerebellar anomalies - childhood onset

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • NHS GMS
    • Expert Review Green
    • Expert list
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • STR
    Green ATXN7_CAG STR in Hereditary ataxia

    Level 3: Motor Disorders of the CNS
    Level 2: Neurology and neurodevelopmental disorders
    Version 1.344

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Expert list
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • STR
    Green ATXN7_CAG STR in Hereditary spastic paraplegia

    Level 3: Motor Disorders of the CNS
    Level 2: Neurology and neurodevelopmental disorders
    Version 1.316

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Expert Review
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • STR
    Amber ATXN7_CAG STR in Childhood onset hereditary spastic paraplegia


    Level 2: Neurology
    Version 8.30
    Latest signed off version: v8.0 (30 Apr 2025)

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • NHS GMS
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • STR
    Green ATXN7_CAG STR in Adult onset hereditary spastic paraplegia


    Level 2: Neurology
    Version 6.7
    Latest signed off version: v6.0 (30 Apr 2025)

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • NHS GMS
    • South West GLH
    • London North GLH
    • Expert Review Green
    • Expert list
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • STR
    Green ATXN7_CAG STR in Adult onset neurodegenerative disorder


    Level 2: Neurology
    Version 8.11
    Latest signed off version: v8.0 (30 Apr 2025)

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Yorkshire and North East GLH
    • NHS GMS
    • South West GLH
    • London North GLH
    • Expert list
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    • autosomal dominant cerebellar ataxia type II, MONDO:0016163
    Tags
    • STR
    No list ATXN7_CAG STR in Undiagnosed metabolic disorders

    Level 3: Specific metabolic abnormalities
    Level 2: Metabolic disorders
    Version 1.642

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • NHS GMS
    • Expert Review Removed
    • Expert list
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • STR
    • curated_removed
    Green ATXN7_CAG STR in Hereditary neuropathy

    Level 3: Motor and Sensory Disorders of the PNS
    Level 2: Neurology and neurodevelopmental disorders
    Version 1.506

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Expert Review
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    • autosomal dominant cerebellar ataxia type II, MONDO:0016163
    Tags
    • STR
    No list ATXN7_CAG STR in Intellectual disability


    Level 2: Developmental disorders
    Version 9.285
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • NHS GMS
    • Expert Review Removed
    • Expert list
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • STR
    • curated_removed
    Green ATXN7_CAG STR in Hereditary ataxia with onset in adulthood


    Level 2: Neurology
    Version 8.23
    Latest signed off version: v8.0 (30 Apr 2025)

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • London North GLH
    • NHS GMS
    • Wessex and West Midlands GLH
    • Expert Review Green
    • Expert list
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • STR
    Green ATXN7_CAG STR in Retinal disorders


    Level 2: Ophthalmology
    Version 8.86
    Latest signed off version: v8.0 (30 Apr 2025)

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    • autosomal dominant cerebellar ataxia type II, MONDO:0016163
    Tags
    • STR
    Green ATXN7_CAG STR in Hereditary neuropathy or pain disorder


    Level 2: Neurology
    Version 7.36
    Latest signed off version: v7.0 (30 Apr 2025)

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Spinocerebellar ataxia 7, OMIM:164500
    Tags
    • STR