1. Genes and Genomic Entities
  2. GSX2

GSX2

GS homeobox 2
OMIM: 616253, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber GSX2 in Intellectual disability


Level 2: Developmental disorders
Version 11.17
Latest signed off version: v11.0 (12 Aug 2026)

Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Diencephalic-mesencephalic junction dysplasia syndrome 2 618646
    • Intellectual disability
    • Dystonia
    • Spastic tetra paresis