HCN2

hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2
OMIM: 602781, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green HCN2 in Early onset or syndromic epilepsy


Level 2: Neurology
Version 8.125
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Wessex and West Midlands GLH
    • NHS GMS
    • Victorian Clinical Genetics Services
    Phenotypes
    • Genetic epilepsy with febrile seizures plus
    • Other seizure disorders