SLC17A3

solute carrier family 17 member 3
OMIM: 611034, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red SLC17A3 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • [Uric acid concentration, serum, QTL4], MIM# 612671, {Gout susceptibility 4}, MIM#612671