SLC7A6OS

solute carrier family 7 member 6 opposite strand
Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SLC7A6OS in Early onset or syndromic epilepsy


Level 2: Neurology
Version 8.176
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Epilepsy, progressive myoclonic, 12 OMIM:619191
    Tags
    • founder-effect