SRPX2

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

4 panels

Panel Reviews Mode of inheritance Details
4 panels

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
  • Expert Review Red
  • Victorian Clinical Genetics Services
  • Australian Genomics Health Alliance Brain Malformations Flagship
Phenotypes
  • Rolandic epilepsy, mental retardation, and speech dyspraxia, MIM# 300643
Tags
  • refuted

Red SRPX2 in Mendeliome


Version 2.0

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

Red SRPX2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Red
  • ClinGen
Phenotypes
  • Epilepsy, MONDO:0005027
Tags
  • refuted

Red SRPX2 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Rolandic epilepsy, mental retardation, and speech dyspraxia, MIM# 300643
Tags
  • refuted