GIGYF2

GRB10 interacting GYF protein 2
OMIM: 612003, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Red GIGYF2 in Parkinson Disease and Complex Parkinsonism

Level 3: Neurodegenerative disorders
Level 2: Neurology and neurodevelopmental disorders
Version 1.128

review Not set
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Susceptibility to Parkinson disease 11, 607688
  • {Parkinson disease 11}
Amber GIGYF2 in Neurodegenerative disorders, adult onset


Level 2: Neurology
Version 9.11
Latest signed off version: v9.4 (12 Aug 2026)

Component of the following Super Panels:

  • Adult-onset neurological disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • NHS GMS
    • Yorkshire and North East GLH
    Phenotypes
    • {Parkinson disease 11}, OMIM:607688
    Red GIGYF2 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.28
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review Not set
    Sources
    • Victorian Clinical Genetics Services
    Red GIGYF2 in Dystonia, chorea or related movement disorder, adult onset


    Level 2: Neurology
    Version 6.9
    Latest signed off version: v6.7 (12 Aug 2026)

    Component of the following Super Panels:

  • Adult-onset neurological disorders
  • review Not set
    Sources
    • NHS GMS
    • South West GLH
    • Expert Review Red
    Phenotypes
    • Susceptibility to Parkinson disease 11, 607688
    • {Parkinson disease 11}