GIGYF2

GRB10 interacting GYF protein 2
OMIM: 612003, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red GIGYF2 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 3.31

Component of the following Super Panels:

  • Movement Disorders Superpanel
  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions
  • 2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • {Parkinson disease 11} , OMIM # 607688

    Green GIGYF2 in Autism


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.13

    2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092, GIGYF2-related

    Green GIGYF2 in Mendeliome


    Version 2.362

    3 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092, GIGYF2-related

    Green GIGYF2 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.61

    1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092, GIGYF2-related