RAC3

Rac family small GTPase 3
OMIM: 602050, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green RAC3 in Polymicrogyria and Schizencephaly


Level 2: Neurology and neurodevelopmental disorders
Version 0.195

Component of the following Super Panels:

  • Malformations of cortical development_Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies, MIM#618577

    Green RAC3 in Mendeliome


    Version 1.2374

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies, MIM#618577

    Green RAC3 in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.119

    Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies, MIM#618577

    Green RAC3 in Callosome


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.540

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies, MIM#618577

    Green RAC3 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.83

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies, MIM#618577