SLC26A6

solute carrier family 26 member 6
OMIM: 610068, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red SLC26A6 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Primary hyperoxaluria, MONDO:0002474, SLC26A6-related