SLC9A3, solute carrier family 9 member A3, 6550

N. diseases: 58; N. variants: 4
Disease: Atrophy of vas deferens ×
Source: BEFREE ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268916
Disease: Atrophy of vas deferens
Atrophy of vas deferens 		0.010 Biomarker phenotype BEFREE SLC9A3 deficiency specifically induces atrophy of vas deferens and unfolding of seminal vesicle mucosa in mice. 30956978 2019