SLC31A1, solute carrier family 31 member 1, 1317

N. diseases: 71; N. variants: 6
Disease: Embryo Disintegration ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1136082
Disease: Embryo Disintegration
Embryo Disintegration 		0.300 Biomarker phenotype CTD_human The copper transporter CTR1 provides an essential function in mammalian embryonic development. 11391004 2001