PanelApp (test)
  1. Genes and Genomic Entities
  2. WAC

WAC

WW domain containing adaptor with coiled-coil
OMIM: 615049, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green WAC in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 0.198

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green WAC in Hypertrichosis syndromes


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.46

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green WAC in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Desanto-Shinawi syndrome, MIM# 616708

Green WAC 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, imprinted status unknown
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Desanto-Shinawi syndrome MIM#616708

    Green WAC in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Desanto-Shinawi syndrome 616708

    Red WAC in Fetal anomalies


    Version 1.255

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    Phenotypes
    • Desanto-Shinawi syndrome, MIM# 616708