CSNK1E

casein kinase 1 epsilon
OMIM: 600863, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Red CSNK1E in Mendeliome


Version 2.590

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Developmental and epileptic encephalopathy, MONDO:0100062, CSNK1E-related

Red CSNK1E in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.42

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Developmental and epileptic encephalopathy, MONDO:0100062, CSNK1E-related

    Amber CSNK1E_FRA22A_CGG STR in Mendeliome


    Version 2.590

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    • Literature
    Phenotypes
    • CSNK1E-related progressive myoclonic epilepsy and developmental and epileptic encephalopathy

    Amber CSNK1E_FRA22A_CGG STR in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.42

    Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    • Literature
    Phenotypes
    • CSNK1E-related progressive myoclonic epilepsy and developmental and epileptic encephalopathy

    Amber CSNK1E_FRA22A_CGG STR in Repeat Disorders


    Version 1.15

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • CSNK1E-related progressive myoclonic epilepsy and developmental and epileptic encephalopathy