SLC31A1, solute carrier family 31 member 1, 1317

N. diseases: 71; N. variants: 6
Disease: Poisoning syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0302332
Disease: Poisoning syndrome
Poisoning syndrome 		0.010 Biomarker disease BEFREE Recently, the gene underlying Wilson disease (ATP7B) as well as copper transport genes hCTR1, hCTR2 and ATOX1 have been excluded as candidates for NICC in man and copper toxicosis in Bedlington terriers. 10425268 1999