CSGALNACT1

chondroitin sulfate N-acetylgalactosaminyltransferase 1
OMIM: 616615, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green CSGALNACT1 in Congenital Disorders of Glycosylation


Level 2: Metabolic disorders
Version 1.44

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Congenital disorder of glycosylation
    • Skeletal dysplasia, mild, with joint laxity and advanced bone age, MIM# 618870

    Green CSGALNACT1 in Mendeliome


    Version 1.1891

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Expert Review
    Phenotypes
    • Skeletal dysplasia, mild, with joint laxity and advanced bone age, MIM# 618870

    Green CSGALNACT1 in Skeletal dysplasia

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 0.285

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Skeletal dysplasia, mild, with joint laxity and advanced bone age, MIM# 618870

    Green CSGALNACT1 in Multiple joint dislocations and laxity

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 0.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Expert Review
    • Victorian Clinical Genetics Services
    • Literature
    Phenotypes
    • Skeletal dysplasia, mild, with joint laxity and advanced bone age, MIM# 618870