CSNK1E

casein kinase 1 epsilon
OMIM: 600863, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red CSNK1E in Mendeliome


Version 1.1891

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 1.33

Component of the following Super Panels:

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