PanelApp
  1. Genes and Genomic Entities
  2. RAB32

RAB32

RAB32, member RAS oncogene family
OMIM: 612906, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber RAB32 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.43

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions
  • Tremors_Superpanel

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • {Parkinson disease 26, autosomal dominant, susceptibility to}, MIM# 620923

    Amber RAB32 in Mendeliome


    Version 1.3512

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • {Parkinson disease 26, autosomal dominant, susceptibility to}, MIM# 620923