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 3: Inherited Epilepsy Syndromes
Level 2: Neurology and neurodevelopmental disorders
Version 4.164
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • 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