FAT2:Ensemblv90

FAT atypical cadherin 2
OMIM: 604269, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green FAT2 in Mendeliome


Version 1.3802

3 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
  • Expert list
  • Royal Melbourne Hospital
  • GeneReviews
Phenotypes
  • Spinocerebellar ataxia 45, MIM#617769

Green FAT2 in Ataxia - adult onset


Level 2: Neurology and neurodevelopmental disorders
Version 1.62

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • 4 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Expert Review Green
    • Expert list
    • Expert list
    • Royal Melbourne Hospital
    • GeneReviews
    Phenotypes
    • Spinocerebellar ataxia 45, MIM#617769

    Green FAT2 in Ataxia


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.162

    Component of the following Super Panels:

  • Ataxia_Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • 4 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • GeneReviews
    • Royal Melbourne Hospital
    • Expert list
    • Expert list
    • Expert Review Green
    • Expert Review Green
    • Expert Review Green
    • Expert Review Green
    • Expert list
    • Expert list
    • Royal Melbourne Hospital
    • GeneReviews
    Phenotypes
    • Spinocerebellar ataxia 45, MIM#617769

    Green FAT2 in Ataxia - adult onset


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.0

    4 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • GeneReviews
    • Royal Melbourne Hospital
    • Expert list
    • Expert list
    • Expert Review Green
    • Expert Review Green
    Phenotypes
    • Spinocerebellar ataxia 45, MIM#617769

    Green FAT2 in Ataxia


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.0

    4 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • GeneReviews
    • Royal Melbourne Hospital
    • Expert list
    • Expert list
    • Expert Review Green
    • Expert Review Green
    • Expert Review Green
    • Expert Review Green
    • Expert list
    • Expert list
    • Royal Melbourne Hospital
    • GeneReviews
    Phenotypes
    • Spinocerebellar ataxia 45, MIM#617769