SLC9A3, solute carrier family 9 member A3, 6550

N. diseases: 58; N. variants: 4
Disease: Spermatocele ×
Source: BEFREE ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037859
Disease: Spermatocele
Spermatocele 		0.010 Biomarker disease 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