PanelApp (staging)
  1. Genes and Genomic Entities
  2. HCN2

HCN2

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

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green HCN2 in Mendeliome


Version 1.2302

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
  • Australian Genomics Health Alliance Epilepsy Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • Febrile seizures, familial, 2, MIM# 602477
  • Genetic epilepsy with febrile seizures plus
  • Other seizure disorders
  • Neurodevelopmental disorder (MONDO#0700092), HCN2-related

Green HCN2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.108

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • Febrile seizures, familial, 2, MIM# 602477
    • Genetic epilepsy with febrile seizures plus
    • Other seizure disorders

    Amber HCN2 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.63

    		1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Other
    Phenotypes
    • Neurodevelopmental disorder (MONDO#0700092), HCN2-related