HOMER2

homer scaffolding protein 2
OMIM: 604799, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber HOMER2 in Monogenic hearing loss


Level 2: Audiology
Version 5.57
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Deafness, autosomal dominant 68, MIM#616707