STARD7

StAR related lipid transfer domain containing 7
OMIM: 616712, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

No list STARD7 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Removed
  • Expert list
Phenotypes
  • Epilepsy, familial adult myoclonic, 2, 607876
Tags
  • STR

No list STARD7 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Removed
    • Literature
    Phenotypes
    • Epilepsy, familial adult myoclonic, 2, 607876
    Tags
    • STR

    Green FAME2 STR in Mendeliome


    Version 1.1891

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Epilepsy, familial adult myoclonic, 2 MIM#607876

    Green FAME2 STR in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.33

    Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Epilepsy, familial adult myoclonic, 2 MIM#607876

    Green FAME2 STR in Repeat Disorders


    Version 0.167

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Epilepsy, familial adult myoclonic, 2 MIM#607876
    Tags
    • adult-onset