NPY, neuropeptide Y, 4852

N. diseases: 381; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE A gain-of-function polymorphism in human neuropeptide Y (<i>NPY</i>) gene (rs16139) associates with metabolic disorders and earlier onset of type 2 diabetes (T2D). 28468933 2017
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE The present study attempts to investigate the association of NPY exon2 +1128 T/C (Leu7Pro; rs16139), NPY promoter -399 T/C (rs16147) and IL1B -511 C/T (rs16944) polymorphisms with TIID and their correlation with plasma lipid levels, BMI, and IL1B transcript levels. 27749914 2016
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE We investigated the associations of inflammatory blood cell activation with vascular parameters in patients with type 2 diabetes to elucidate the possible mechanisms of accelerated atherosclerosis observed in subjects with the Leucine 7 to Proline 7 polymorphism (Leu7Pro) in the neuropeptide Y (NPY). 21746772 2011
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE The Leu7Pro polymorphism of the signal peptide of neuropeptide Y (NPY) gene is associated with increased levels of inflammatory markers preceding vascular complications in patients with type 2 diabetes. 20691708 2010
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE The leucine7 to proline7 (Leu7Pro) polymorphism in preproneuropeptide Y (preproNPY) has been associated with accelerated atherosclerosis and type II diabetes, both of which are obesity-related diseases. 18043699 2009
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE Leu7Pro polymorphism of PreproNPY associated with an increased risk for type II diabetes in middle-aged subjects. 17268419 2007
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE Since no impact of preproNPY genotype on mean NPY or hormone levels were detected in subjects with type 2 diabetes, the mechanisms for the increased risk for diabetic complications in the subjects with the Leu7Pro polymorphism need to be further explored. 17516289 2007
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE These results suggest that the Leu7Pro polymorphism could be used to predict earlier onset of type 2 diabetes and retinopathy, and increased risk for diabetic nephropathy. 16705546 2006
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE The present study thus provides the evidence that Leu7Pro polymorphism in the NPY gene is associated with IGT and T2DM in Swedish men, and indicates that the NPY gene variations contribute to development of T2DM. 15926114 2005
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE Leucine 7 to proline 7 polymorphism in the neuropeptide Y gene is associated with enhanced carotid atherosclerosis in elderly patients with type 2 diabetes and control subjects. 10852461 2000
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE Leucine 7 to proline 7 polymorphism in the neuropeptide y gene is associated with retinopathy in type 2 diabetes. 10926322 2000
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0028754
Disease:
Obesity
0.050 GeneticVariation BEFREE This study suggests that NPY rs16147 T and rs16139 C minor alleles are associated with increased risk, whereas the minor allele T of the rs5574 is associated with a reduced risk of obesity. 26240981 2015
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0010068
Disease:
Coronary heart disease
0.050 GeneticVariation BEFREE Neuropeptide Y Leu7Pro polymorphism associated with the metabolic syndrome and its features in patients with coronary artery disease. 22308535 2013
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.050 GeneticVariation BEFREE Neuropeptide Y Leu7Pro polymorphism associated with the metabolic syndrome and its features in patients with coronary artery disease. 22308535 2013
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0028754
Disease:
Obesity
0.050 GeneticVariation BEFREE In this study, we investigated the role of two functional NPY polymorphisms, NPY-Leu7Pro (rs16139) and NPY-399C/T (rs16147) and obesity for the development of asthma as well as atherosclerosis in asthmatic and non-asthmatic subjects. 23122776 2012
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0010068
Disease:
Coronary heart disease
0.050 GeneticVariation BEFREE High frequency of Neuropeptide Y Leu7Pro polymorphism in an Iranian population and its association with coronary artery disease. 22289186 2012
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.050 GeneticVariation BEFREE High frequency of Neuropeptide Y Leu7Pro polymorphism in an Iranian population and its association with coronary artery disease. 22289186 2012
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0028754
Disease:
Obesity
0.050 GeneticVariation BEFREE Two SNPs (rs17149106 (G>T) and rs16139 (T>C)), with minor allele frequencies of 4%, were associated with elevated risks of obesity (BMI ≥ 30 kg/m(2)) in both cohorts. 21937627 2011
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0028754
Disease:
Obesity
0.050 GeneticVariation BEFREE In 6 years follow-up, the polymorphism alone did not change the risk for abnormal glucose regulation, while obesity</span> was associated with a significant 3-fold risk (odds ratio (OR) 2.95; 95% confidence interval (CI) 1.81-4.81, P<0.001) and the Leu7Pro polymorphism-obesity interaction, with a remarkable 12-fold risk (OR 12.33; 95% CI 1.18-128.35, P<0.05). 18043699 2009
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.050 GeneticVariation BEFREE The aim of the present study was to investigate the association of the Leu7Pro polymorphism with coronary atherosclerosis and its consequences. 18054939 2008
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0010068
Disease:
Coronary heart disease
0.050 GeneticVariation BEFREE The Leu7Pro substitution has been linked to cardiovascular disease, but it is unknown whether the Pro7 allele is associated with increased or decreased risk of coronary heart disease (CHD). 18054939 2008
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0028754
Disease:
Obesity
0.050 GeneticVariation BEFREE The consistent findings among men suggest that the NPY Leu7Pro polymorphism (or another linked marker) might be involved in the development of obesity at younger ages. 16568137 2006
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.050 GeneticVariation BEFREE Leucine 7 to proline 7 polymorphism in the preproneuropeptide Y is associated with proteinuria, coronary heart disease, and glycemic control in type 1 diabetic patients. 14747236 2004
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0010068
Disease:
Coronary heart disease
0.050 GeneticVariation BEFREE We conclude that the Leu7Pro polymorphism may contribute to the genetic susceptibility to diabetic nephropathy and CHD in type 1 diabetic patients, possibly by influencing glycemic control and triglycerides. 14747236 2004
dbSNP: rs16139
rs16139
Entrez Id: 4852;107986777
Gene Symbol: NPY;LOC107986777
NPY;LOC107986777
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.050 GeneticVariation BEFREE Association of leucine 7 to proline 7 polymorphism in the preproneuropeptide Y with serum lipids in patients with coronary heart disease. 11914038 2002