YBX3

Y-box binding protein 3
OMIM: 603437, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red YBX3 in Intellectual disability


Level 2: Developmental disorders
Version 11.7
Latest signed off version: v11.0 (12 Aug 2026)

Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Literature
    Phenotypes
    • Neurological disorder