Human | XYLT2 | 64132 | xylosyltransferase II | |
Human | XYLT1 | 64131 | xylosyltransferase I | |
Human | ADIPOQ | 9370 | adiponectin, C1Q and collagen domain containing | Multiple logistic regression analysis identified sex, angina pectoris, and PAI-1 as independent determinants of hyperadiponectinemia |
Human | PLA2G7 | 7941 | phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) | Title:Vasospastic Angina and Microvascular Angina are Differentially Influenced by PON1 A632G Polymorphism in the Japanese.|Association:Not Found|Conclusion:There was a significant association between PON1 A632G polymorphism and MVA as well as VSA, but the impact of this on VSA and MVA is different in the Japanese. |
Human | TNNI3 | 7137 | troponin I type 3 (cardiac) | INFERRED, Score=800, UMLKSK CUI: C0002962 |
Human | TNF | 7124 | tumor necrosis factor | INFERRED, Score=800, UMLKSK CUI: C0002962 |
Human | TLR4 | 7099 | toll-like receptor 4 | INFERRED, Score=800, UMLKSK CUI: C0002962 |
Human | TAF1 | 6872 | TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa | Title:Association between thrombin-activatable fibrinolysis inhibitor (TAFI) and clinical outcome in patients with unstable angina pectoris.|Association:Y|Conclusion:In conclusion, in this study population plasma TAFI Ag levels are significantly correlated with refractiveness in patients with UAP. Furthermore, all three polymorphisms contribute independently to plasma TAFI Ag levels, but not to refractiveness. |
Human | SREBF1 | 6720 | sterol regulatory element binding transcription factor 1 | INFERRED, Score=800, UMLKSK CUI: C0002962 |
Human | CCL3 | 6348 | chemokine (C-C motif) ligand 3 | INFERRED, Score=800, UMLKSK CUI: C0002962 |
Human | PTX3 | 5806 | pentraxin 3, long | INFERRED, Score=800, UMLKSK CUI: C0002962 |
Human | PON1 | 5444 | paraoxonase 1 | Title:Vasospastic Angina and Microvascular Angina are Differentially Influenced by PON1 A632G Polymorphism in the Japanese.|Association:Not Found|Conclusion:There was a significant association between PON1 A632G polymorphism and MVA as well as VSA, but the impact of this on VSA and MVA is different in the Japanese. |
Human | PLA2G2A | 5320 | phospholipase A2, group IIA (platelets, synovial fluid) | Data show that serum concentrations of PLA(2)-IIA, Lp(a), ICAM-1 and PECAM-1 are higher for patients with unstable rather that stable angina and controls, and that high plasma Lp(a) is an independent risk factor for angina |
Human | SERPINE1 | 5054 | serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 | Multiple logistic regression analysis identified sex, angina pectoris, and PAI-1 as independent determinants of hyperadiponectinemia |
Human | NOS3 | 4846 | nitric oxide synthase 3 (endothelial cell) | Title:Endothelial nitric oxide synthase gene polymorphism (Glu298Asp) in patients with coexistent hypertrophic cardiomyopathy and coronary spastic angina.|Association:Y|Conclusion:In conclusion, the Asp298 variant of the eNOS gene may be associated with CSA in HCM patients. HCM patients with CSA or the Asp298 variant may need more drugs to relieve their symptoms. |
Human | NFKBIL1 | 4795 | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 1 | no association between polymorphisms and hypertension, myocardial infarct and angina in Irish |
Human | MMP9 | 4318 | matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) | Title:The roles of stromelysin-1 and the gelatinase B gene polymorphism in stable angina.|Association:Not Found|Conclusion:Our results show that functional genetic variation of stromelysin-1 could be a significant risk factor for stable angina, and might play an important role in coronary atherosclerosis involving vascular remodeling. |
Human | MMP3 | 4314 | matrix metallopeptidase 3 (stromelysin 1, progelatinase) | Title:The roles of stromelysin-1 and the gelatinase B gene polymorphism in stable angina.|Association:Not Found|Conclusion:Our results show that functional genetic variation of stromelysin-1 could be a significant risk factor for stable angina, and might play an important role in coronary atherosclerosis involving vascular remodeling. |
Human | LTA | 4049 | lymphotoxin alpha | no association between polymorphisms and hypertension, myocardial infarct and angina in Irish |
Human | LMNA | 4000 | lamin A/C | |
Human | LEP | 3952 | leptin | INFERRED, Score=800, UMLKSK CUI: C0002962 |
Human | ITGB3 | 3690 | integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) | INFERRED, Score=800, UMLKSK CUI: C0002962 |
Human | ITGA3 | 3675 | integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor) | Title:Association of genetic polymorphisms in the fibrinogen and platelet glycoprotein genes with unstable angina in Chinese patients|Association:Not Found|Conclusion:Chinese patients with UA had increased frequencies of GP Ib alpha C/B genotype and Bbeta fibrinogen 448A allele. These data suggest that some genetic factors may influence the development of UA. |
Human | IL18 | 3606 | interleukin 18 (interferon-gamma-inducing factor) | INFERRED, Score=800, UMLKSK CUI: C0002962 |
Human | IL6 | 3569 | interleukin 6 (interferon, beta 2) | INFERRED, Score=800, UMLKSK CUI: C0002962 |