PanelApp (test)
  1. Genes and Genomic Entities
  2. KCNT2

KCNT2

potassium sodium-activated channel subfamily T member 2
OMIM: 610044, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green KCNT2 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Epileptic encephalopathy, early infantile, 57, MIM#617771
  • Developmental and epileptic encephalopathy
  • Epilepsy of infancy with migrating focal seizures (EIMFS)

Green KCNT2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    • Expert Review Green
    • Literature
    Phenotypes
    • Epileptic encephalopathy, early infantile, 57, MIM#617771
    • Developmental and epileptic encephalopathy

    Green KCNT2 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Epileptic encephalopathy, early infantile 57, 617771