HCN2

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

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green HCN2 in Genetic epilepsy syndromes

Level 3: Inherited Epilepsy Syndromes
Level 2: Neurology and neurodevelopmental disorders
Version 2.572
Latest signed off version: v2.2 (13 Feb 2020)

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

Green HCN2 in Severe Paediatric Disorders


Version 1.127

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Next Generation Children Project
  • Expert Review Green
  • Expert list
Phenotypes
  • Febrile seizures