KCNC2

potassium voltage-gated channel subfamily C member 2
OMIM: 176256, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green KCNC2 in Early onset or syndromic epilepsy


Level 2: Neurology
Version 9.8
Latest signed off version: v9.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • epileptic encephalopathy
    • spastic tetraplegia
    • opisthotonus attacks
    • intellectual disability
    • West syndrome