PanelApp (stage)
  1. Genes and Genomic Entities
  2. SCYL2

SCYL2

SCY1 like pseudokinase 2
OMIM: 616365, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber SCYL2 in Arthrogryposis


Level 2: Neurology and neurodevelopmental disorders
Version 0.411

Component of the following Super Panels:

  • Neuromuscular Superpanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Arthrogryposis multiplex congenita (AMC)
    • Zain syndrome

    Amber SCYL2 in Mendeliome


    Version 1.1891

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Arthrogryposis multiplex congenita (AMC)
    • Zain syndrome

    Amber SCYL2 in Fetal anomalies


    Version 1.255

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    • Expert list
    Phenotypes
    • Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum - #618766