Gene: SLC2A6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11182
Gene Symbol: SLC2A6
SLC2A6 		0.020 GeneticVariation disease BEFREE A novel homozygous GLUT9 mutation cause recurrent exercise-induced acute renal failure and posterior reversible encephalopathy syndrome. 24643436 2015
Entrez Id: 11182
Gene Symbol: SLC2A6
SLC2A6 		0.020 GeneticVariation disease BEFREE In conclusion, homozygous loss-of-function mutations of GLUT9 cause a total defect of uric acid absorption, leading to severe renal hypouricemia complicated by nephrolithiasis and exercise-induced acute renal failure. 19926891 2010