SLC26A1, solute carrier family 26 member 1, 10861

N. diseases: 33; N. variants: 24
Disease: NEPHROLITHIASIS, CALCIUM OXALATE ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in SLC26A1 Cause Nephrolithiasis. 27210743 2016
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE 		0.700 GeneticVariation disease UNIPROT Mutations in SLC26A1 Cause Nephrolithiasis. 27210743 2016
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE 		0.700 Biomarker disease GENOMICS_ENGLAND Urolithiasis and hepatotoxicity are linked to the anion transporter Sat1 in mice. 20160351 2010
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE 		0.700 Biomarker disease CTD_human
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE 		0.700 Biomarker disease HPO