potassium voltage-gated channel subfamily A member 4
OMIM: 176266, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red KCNA4 in Familial Meniere Disease

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.1

review Not set
  • Literature

Red KCNA4 in DDG2P

Version 2.11
Signed off v.2.2 on 13 Feb 2020

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    • Expert Review Red
    • DD-Gene2Phenotype
    • KCN4 related abnormal striatum, congenital cataract and intellectual disability.