KCTD3

potassium channel tetramerization domain containing 3
OMIM: 613272, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green KCTD3 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Epilepsy
  • Intellectual disability
  • Posterior fossa abnormalities

Green KCTD3 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • Epilepsy
    • Intellectual disability
    • Posterior fossa abnormalities

    Green KCTD3 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Epilepsy
    • Intellectual disability
    • Posterior fossa abnormalities