GIGYF2

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

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red GIGYF2 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 3.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • {Parkinson disease 11} , OMIM # 607688

Red GIGYF2 in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

1 review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services

Red GIGYF2 in Mendeliome


Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • {Parkinson disease 11} MIM#607688