SLC26A8

solute carrier family 26 member 8
OMIM: 608480, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green SLC26A8 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • non-syndromic male infertility due to sperm motility disorder MONDO:0017173