SLC19A2, solute carrier family 19 member 2, 10560

N. diseases: 70; N. variants: 15
Disease: Beriberi ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005122
Disease: Beriberi
Beriberi 		0.020 Biomarker disease BEFREE Our findings on SLC19A2 and SLC19A3 suggest a potential role of these two genes in the pathophysiology of alcohol-related thiamine deficiency but further studies need to be carried out. 19096015 2009
CUI: C0005122
Disease: Beriberi
Beriberi 		0.020 Biomarker disease BEFREE Characterization of the metabolic defect of TRMA may shed light on the role of thiamine deficiency in such common diseases. 9399900 1997