HCN1

hyperpolarization activated cyclic nucleotide gated potassium channel 1
OMIM: 602780, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green HCN1 in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 0.205

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green HCN1 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Developmental and epileptic encephalopathy 24, MIM# 615871
  • Generalized epilepsy with febrile seizures plus, type 10, MIM# 618482

Green HCN1 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.119

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • Developmental and epileptic encephalopathy 24, MIM# 615871
    • Generalized epilepsy with febrile seizures plus, type 10, MIM# 618482

    Green HCN1 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.83

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Developmental and epileptic encephalopathy 24, MIM# 615871
    • Generalized epilepsy with febrile seizures plus, type 10, MIM# 618482