EXOC7

exocyst complex component 7
OMIM: 608163, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green EXOC7 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with seizures and brain atrophy MIM#619072
  • brain atrophy
  • seizures
  • developmental delay
  • microcephaly

Green EXOC7 in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.269

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • brain atrophy
  • seizures
  • developmental delay
  • microcephaly

Green EXOC7 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Expert Review Green
    • Literature
    Phenotypes
    • brain atrophy
    • seizures
    • developmental delay
    • microcephaly

    Green EXOC7 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • brain atrophy
    • seizures
    • developmental delay
    • microcephaly

    Green EXOC7 in Fetal anomalies


    Version 1.255

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with seizures and brain atrophy MIM#619072