SLC9A3, solute carrier family 9 member A3, 6550

N. diseases: 73; N. variants: 15
Disease: Subfertility, Male ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0848676
Disease: Subfertility, Male
Subfertility, Male 		0.010 AlteredExpression phenotype BEFREE Tissue-specific co-expression with CFTR and NHE3 supports diverse functions of SLC26A3 and may have an impact on pathophysiology of male subfertility both in CLD and in cystic fibrosis (CF), as well as spermatoceles. 16421216 2006