Human | LOC100507436 | 100507436 | | Click here to display 10 evidence detail records. |
Human | KIR2DS2 | 100132285 | killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 2 | Title:|Association:Y|Conclusion:Not Found Title:Killer cell immunoglobulin-like receptor genes in Latvian patients with type 1 diabetes mellitus and healthy controls.|Association:Not Found|Conclusion:In conclusion, our results suggest that a balance between innate and acquired immunity is important, and an imbalance coud lead to T1DM. |
Human | ZGLP1 | 100125288 | zinc finger, GATA-like protein 1 | A disturbed GLP-1 secretion does not play a role in blunting the insulin response observed in patients with diabetes and liver cirrhosis |
Human | CCR2 | 729230 | chemokine (C-C motif) receptor 2 | Title:Polymorphisms of chemokine and chemokine receptor genes in Type 1 diabetes mellitus and its complications.|Association:Y|Conclusion:These results suggest that polymorphisms of the MCP-1, CCR2 and CCR5 genes may be associated with T1DM and its complications. |
Human | SUMO4 | 387082 | small ubiquitin-like modifier 4 | Title:Preliminary studies on associations of IDDM3, IDDM4, IDDM5 and IDDM8 with IDDM in Chengdu population.|Association:Not Found|Conclusion:IDDM3, IDDM4, IDDM5 but not IDDM8 may be associated with IDDM in Chinese Han nationality population. Title:|Association:Y|Conclusion:Not Found |
Human | ZFP57 | 346171 | ZFP57 zinc finger protein | Late predisposition to type 2 (insulin resistant) diabetes |
Human | VWA2 | 340706 | von Willebrand factor A domain containing 2 | Single nucleotide polymorphisms in the AMACO gene are associated with dominant protection against Type 1A diabetes in an Arab family |
Human | CRTC2 | 200186 | CREB regulated transcription coactivator 2 | Dysregulation of the TSC-mTOR pathway may cause not only tumor development but also metabolic disorders such as diabetes and its comp |
Human | PPARGC1B | 133522 | peroxisome proliferator-activated receptor gamma, coactivator 1 beta | Recent studies have elucidated the function of the PGC-1 coactivators in different tissues and have highlighted the implications of PGC-1 dysregulation in diseases such as diabetes, obesity, cardiomyopathy, or neurodegeneration |
Human | CYP2R1 | 120227 | cytochrome P450, family 2, subfamily R, polypeptide 1 | Title:CYP2R1 (vitamin D 25-hydroxylase) gene is associated with susceptibility to type 1 diabetes and vitamin D levels in Germans|Association:Y|Conclusion:Thus, our findings reveal a novel association of CYP2R1 polymorphisms in patients with type 1 diabetes and with their circulating levels of 25(OH)D(3). |
Human | APOA5 | 116519 | apolipoprotein A-V | APOA5 could also influence cholesterol homeostasis and probably play a role in hypertriglyceridemia associated with diabetes and inflammation |
Human | Gma3 | 110204 | granulocyte macrophage antigen 3 | Title:|Association:Not Found|Conclusion:Not Found |
Human | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Overexpression of human DGAT2 in glycolytic muscle of mice promotes insulin resistance in this tissue and may contribute to the development of diabetes |
Human | PCBD2 | 84105 | pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 2 | Title:|Association:Not Found|Conclusion:Not Found |
Human | SETD7 | 80854 | SET domain containing (lysine methyltransferase) 7 | a novel role for SET7/9 in inflammation and diabetes |
Human | ADIPOR2 | 79602 | adiponectin receptor 2 | Upregulation in endothelial cells potentiates the antiinflammatory effect of adiponectin, which may apply to cardiovascular complcation in diabetes Title:|Association:Not Found|Conclusion:Not Found |
Human | FTO | 79068 | fat mass and obesity associated | A genome-wide search for type 2 diabetes-susceptibility genes identified a common variant in the FTO gene that predisposes to diabetes through an effect on body mass index |
Human | HPSE2 | 60495 | heparanase 2 | Data suggest that loss of modified heparan sulphate in the GBM is mediated by an increased heparanase presence and may play a role in the pathogenesis of diabetes-induced proteinuria |
Human | HRH4 | 59340 | histamine receptor H4 | Results describe the expression of histamine H4 receptors in normal placentas and in placentas from pregnancies complicated by pregestational diabetes |
Human | G6PC2 | 57818 | glucose-6-phosphatase, catalytic, 2 | Alpha mutants containing the beta cell antigen sequence are preferentially degraded in cells, which prevents targeting by pathogenic CD8+ T cells implying that IGRP levels in beta cells could dictate susceptibilities to diabetes |
Human | HYMAI | 57061 | hydatidiform mole associated and imprinted (non-protein coding) | Late predisposition to type 2 (insulin resistant) diabetes imprinted in transient neonatal diabetes |
Human | RETN | 56729 | resistin | Title:Systematic search for single nucleotide polymorphisms in the resistin gene: the absence ofevidence for the association of three identified single nucleotide polymorphisms with Japanese type 2 diabetes.|Association:Not Found|Conclusion:These identified SNPs, which were in linkage disequilibrium, represent potentially useful tools for searching for their association with specific phenotypes of diabetes. In adults with hypertension, higher circulating resistin levels were associated with a lower estimated glomerular filtration rate and with increased urine albumin:creatinine ratio in the presence of concomitant diabetes Title:|Association:Not Found|Conclusion:Not Found Resistin inhibition may not represent a suitable therapeutic strategy for the treatment of insulin resistance and diabetes in patients with liver cirrhosis |
Human | CDKAL1 | 54901 | CDK5 regulatory subunit associated protein 1-like 1 | Diabetes-associated variants in TCF7L2 and CDKAL1 impair insulin secretion and conversion of proinsulin to insulin |
Human | GHRL | 51738 | ghrelin/obestatin prepropeptide | Title:Preproghrelin Leu72Met polymorphism in patients with type 2 diabetes mellitus.|Association:Not Found|Conclusion:The Leu72Met polymorphism of the preproghrelin gene was not related to cardiovascular disease in type 2 diabetes mellitus patients. Leu72Met polymorphism was, however, associated with serum creatinine and Lp(a) levels in diabetic patients. The mechanism might be associated with a possible change in ghrelin product and its somatotropic effect. |
Human | KLF13 | 51621 | Kruppel-like factor 13 | Title:Single nucleotide polymorphisms in the gene encoding Kr????ppel-like factor 7 are associated with type 2 diabetes.|Association:Not Found|Conclusion:These results indicate that the gene encoding KLF7 is a novel candidate for conferring genetic susceptibility to type 2 diabetes. |