KCNK17

potassium two pore domain channel subfamily K member 17
OMIM: 607370, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red KCNK17 in Progressive cardiac conduction disease


Version 2.6
Latest signed off version: v2.2 (22 Mar 2023)

Component of the following Super Panels:

  • Sudden unexplained death or survivors of a cardiac event
  • review Unknown
    Sources
    • South West GLH
    Phenotypes
    • Heart conduction disease, MONDO:0000992