DSCAM

DS cell adhesion molecule
OMIM: 602523, ClinGen, DECIPHER

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Amber DSCAM in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 1.13

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Autism

Green DSCAM in Mendeliome


Version 2.336

2 reviews BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Neurodevelopmental disorder (MONDO:0700092), DSCAM-related
  • Autism MONDO:0005260

Green DSCAM in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.28

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder (MONDO:0700092), DSCAM-related

    Red DSCAM in Callosome


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.6

    1 review Unknown
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services

    Green DSCAM in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.53

    2 reviews BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Neurodevelopmental disorder (MONDO:0700092), DSCAM-related
    • Autism MONDO:0005260

    Green DSCAM in Syndromic Retinopathy


    Level 2: Ophthalmological disorders
    Version 1.2

    Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder (MONDO:0700092), DSCAM-related