PanelApp (test)
  1. Genes and Genomic Entities
  2. MYO9B:Ensemblv90

MYO9B:Ensemblv90

myosin IXB
OMIM: 602129, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber MYO9B in Mendeliome


Version 1.3802

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Charcot-Marie-Tooth disease type 2 (MONDO:0018993), MYO9B-related

Amber MYO9B in Hereditary Neuropathy_CMT - isolated


Level 2: Neurology and neurodevelopmental disorders
Version 1.68

Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Charcot-Marie-Tooth disease type 2 (MONDO:0018993), MYO9B-related

    Amber MYO9B in Hereditary Neuropathy_CMT - isolated


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.0

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    • Expert Review Amber
    Phenotypes
    • Charcot-Marie-Tooth disease type 2 (MONDO:0018993), MYO9B-related