SLC7A6OS

solute carrier family 7 member 6 opposite strand
Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red SLC7A6OS in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Epilepsy, progressive myoclonic, 12, MIM# 619191

Red SLC7A6OS 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 Red
    • Literature
    Phenotypes
    • Epilepsy, progressive myoclonic, 12, MIM# 619191
    • Progressive myoclonus epilepsy

    Red SLC7A6OS in Progressive Myoclonic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.19

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Epilepsy, progressive myoclonic, 12, MIM# 619191