PanelApp (staging)
  1. Genes and Genomic Entities
  2. C1orf194

C1orf194

chromosome 1 open reading frame 194
ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber C1orf194 in Mendeliome


Version 1.2302

3 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Charcot-Marie-Tooth disease, intermediate or demyelinating, MONDO:0015626, C1orf194-related

Amber C1orf194 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

    		•  3 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    • Literature
    Phenotypes
    • Charcot-Marie-Tooth disease, intermediate or demyelinating