KCNJ15

potassium voltage-gated channel subfamily J member 15
OMIM: 602106, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red KCNJ15 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.38

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions
  • Tremors_Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Parkinson disease, MONDO:0005180, KCNJ15-related

    Red KCNJ15 in Mendeliome


    Version 1.3098

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Parkinson disease, MONDO:0005180, KCNJ15-related