PanelApp (stage)
  1. Genes and Genomic Entities
  2. CHST8

CHST8

carbohydrate sulfotransferase 8
OMIM: 610190, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red CHST8 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 Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Peeling Skin Syndrome

    Red CHST8 in Mendeliome


    Version 1.1891

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Peeling skin syndrome, MONDO:0019347, CHST8-realted