STX4

syntaxin 4
OMIM: 186591, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber STX4 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 BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Hearing impairment, HP:0000365