SLC2A9, solute carrier family 2 member 9, 56606

N. diseases: 74; N. variants: 389
Disease: Parkinson Disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.040 Biomarker disease BEFREE We did not find significant associations between the SNPs in SLC2A9 and PD risk among men or women. 29789205 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.040 Biomarker disease BEFREE Our findings suggest that Glut9 could be modified to modulate urate levels in dopaminergic neurons and urate-elevating strategies without increasing systemic levels to avoid side effects might serve as a potential therapeutic target for PD. 29434538 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.040 GeneticVariation disease BEFREE Thus, SLC2A9 rs1014290 is related to lower uric acid levels in PD patients and can be a risk factor for PD in the Han population. 29158942 2017
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.040 GeneticVariation disease BEFREE Our study suggests that SLC2A9 genetic variants influence age of onset of Parkinson's disease. 20589538 2011