SRPX2

sushi repeat containing protein X-linked 2
OMIM: 300642, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red SRPX2 in Polymicrogyria and Schizencephaly


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

2 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Australian Genomics Health Alliance Brain Malformations Flagship
  • Victorian Clinical Genetics Services
  • Expert Review Red
Phenotypes
  • Rolandic epilepsy, mental retardation, and speech dyspraxia, MIM# 300643
Tags
  • refuted