XYLT2, xylosyltransferase 2, 64132

N. diseases: 138; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.040 GeneticVariation disease BEFREE The haplotype analysis of 6 XYLT2 polymorphisms revealed one haplotype (GATTCG) to be significantly less frequent among type 1 patients with diabetic nephropathy (p=0.002, OR=0.13, 95% CI=0.03-0.59). 18789912 2008
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.040 GeneticVariation disease BEFREE Furthermore, sequence variations in the XT-I and XT-II coding genes were identified as risk factors for diabetic nephropathy, osteoarthritis or pseudoxanthoma elasticum. 17437056 2007
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.040 GeneticVariation disease BEFREE Genotyping of four genetic variations in the genes XYLT-I and XYLT-II was performed in 912 type 1 diabetic patients (453 with and 459 without diabetic nephropathy) using restriction fragment-length polymorphism. 17003309 2006
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.040 Biomarker disease LHGDN Impact of polymorphisms in the genes encoding xylosyltransferase I and a homologue in type 1 diabetic patients with and without nephropathy. 16164625 2005