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 0.416

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Arthrogryposis multiplex congenita (AMC)
  • Zain syndrome
Amber SCYL2 in Mendeliome


Version 1.2302

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Arthrogryposis multiplex congenita (AMC)
  • Zain syndrome
Amber SCYL2 in Fetal anomalies


Version 1.313

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