A4GALT

alpha 1,4-galactosyltransferase (P blood group)
OMIM: 607922, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list A4GALT in Congenital disorders of glycosylation


Level 2: Metabolic
Version 7.13
Latest signed off version: v7.0 (30 Apr 2025)

Component of the following Super Panels:

  • Hereditary ataxia and cerebellar anomalies - childhood onset
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Removed
    • ClinGen
    Phenotypes
    • [Blood group, P1Pk system, p phenotype], OMIM:111400
    Tags
    • curated_removed