1. Genes and Genomic Entities
  2. GSTZ1

GSTZ1

glutathione S-transferase zeta 1
OMIM: 603758, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber GSTZ1 in Likely inborn error of metabolism - targeted testing not possible


Version 5.1
Latest signed off version: v5.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Eligibility statement prior genetic testing
    • Expert Review
    • Literature
    Phenotypes
    • [Maleylacetoacetate isomerase deficiency], OMIM:617596
    Tags
    • Q1_24_promote_green
    • Q1_24_NHS_review