PanelApp (staging)
  1. Genes and Genomic Entities
  2. GNB4

GNB4

G protein subunit beta 4
OMIM: 610863, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green GNB4 in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Charcot-Marie-Tooth disease, dominant intermediate F, MIM# 615185
  • MONDO:0014074

Green GNB4 in Hereditary Neuropathy_CMT - isolated


Level 2: Neurology and neurodevelopmental disorders
Version 1.51

Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Charcot-Marie-Tooth disease, dominant intermediate F, MIM# 615185
    • MONDO:0014074
    • HMSN