PanelApp
  1. Genes and Genomic Entities
  2. ARHGAP19

ARHGAP19

Rho GTPase activating protein 19
OMIM: 611587, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green ARHGAP19 in Mendeliome


Version 1.4216

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Charcot-Marie-Tooth disease, axonal, type 2KK, MIM# 621466

Green ARHGAP19 in Hereditary Neuropathy_CMT - isolated


Level 2: Neurology and neurodevelopmental disorders
Version 1.77

Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Literature
    Phenotypes
    • Charcot-Marie-Tooth disease, axonal, type 2KK, MIM# 621466