PREX1

phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 1
OMIM: 606905, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red PREX1 in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 1.18

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Literature
Phenotypes
  • Neurodevelopmental disorder (MONDO:0700092), PREX1-related

Red PREX1 in Mendeliome


Version 2.516

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
Phenotypes
  • Neurodevelopmental disorder (MONDO:0700092), PREX1-related

Red PREX1 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.38

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Literature
    • Literature
    Phenotypes
    • Neurodevelopmental disorder (MONDO:0700092), PREX1-related

    Red PREX1 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.125

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Literature
    • Literature
    Phenotypes
    • Neurodevelopmental disorder (MONDO:0700092), PREX1-related