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DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10634821-2#140#145#geners137853240 449-454 geners137853240 denotes G319S
10634821-2#229#244#diseaseC0011860 538-553 diseaseC0011860 denotes type 2 diabetes
10634821-2#289#304#diseaseC0011860 598-613 diseaseC0011860 denotes type 2 diabetes
140#145#geners137853240229#244#diseaseC0011860 10634821-2#140#145#geners137853240 10634821-2#229#244#diseaseC0011860 associated_with G319S,type 2 diabetes
140#145#geners137853240289#304#diseaseC0011860 10634821-2#140#145#geners137853240 10634821-2#289#304#diseaseC0011860 associated_with G319S,type 2 diabetes

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10634821-7#53#58#gene6927 1427-1432 gene6927 denotes HNF1A
10634821-7#143#158#diseaseC0011860 1517-1532 diseaseC0011860 denotes type 2 diabetes
53#58#gene6927143#158#diseaseC0011860 10634821-7#53#58#gene6927 10634821-7#143#158#diseaseC0011860 associated_with HNF1A,type 2 diabetes

2015-BEL-Sample-2

Id Subject Object Predicate Lexical cue
BEL:20042214 0-1610 p(HGNC:HNF1A) increases r(HGNC:NPM1) denotes The private hepatocyte nuclear factor-1alpha G319S variant is associated with plasma lipoprotein variation in Canadian Oji-Cree. We previously showed an extremely strong association between type 2 diabetes and a private polymorphism, namely G319S, in the hepatocyte nuclear transcription factor (HNF)-1alpha. Because HNF-1alpha is involved in the transcription of several apolipoprotein genes, we tested for an association between the private HNF1A G319S variant and plasma lipoproteins in a sample of 55 unrelated Oji-Cree subjects with type 2 diabetes and 175 unrelated Oji-Cree subjects without type 2 diabetes. In Oji-Cree subjects with type 2 diabetes, we found that the HNF1A G319S genotype was significantly associated with lower plasma concentrations of total cholesterol, low density lipoprotein cholesterol, and apolipoprotein (apo) B. In Oji-Cree subjects without type 2 diabetes, we found that the HNF1A G319S genotype was significantly associated with higher plasma concentrations of high density lipoprotein cholesterol and apo AI. There were no associations with plasma triglycerides or lipoprotein(a). Regression analysis indicated that the HNF1A genotype accounted for approximately 10% of the variation in the apo B-related traits in the diabetic subjects and for approximately 5% of the variation in the apo AI-related traits in the nondiabetic subjects. Furthermore, the regression model indicated that the HNF1A S319 allele affected these traits in a dominant manner in subjects with and without type 2 diabetes. These findings provide the first evidence that a rare variant in a nuclear t

DisGeNET

Id Subject Object Predicate Lexical cue
T0 443-448 gene:6927 denotes HNF1A
T1 538-553 disease:C0011860 denotes type 2 diabetes
T2 443-448 gene:6927 denotes HNF1A
T3 598-613 disease:C0011860 denotes type 2 diabetes
R1 T0 T1 associated_with HNF1A,type 2 diabetes
R2 T2 T3 associated_with HNF1A,type 2 diabetes