SOBP

sine oculis binding protein homolog
OMIM: 613667, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SOBP in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Mental retardation, anterior maxillary protrusion, and strabismus, MIM# 613671

Red SOBP in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Mental retardation, anterior maxillary protrusion, and strabismus, MIM# 613671