GABRA6

gamma-aminobutyric acid type A receptor alpha6 subunit
OMIM: 137143, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red GABRA6 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Benign familial inherited epilepsy
  • Childhood absence epilepsy

Red GABRA6 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
    • Literature
    Phenotypes
    • BFIE
    • CAE