Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1401
Gene Symbol: CRP
CRP
0.600 Biomarker disease RGD [Preliminary investigation of the changes and mechanism of Leptin after myocardial ischemia/reperfusion injury]. 21122204 2010
Entrez Id: 959
Gene Symbol: CD40LG
CD40LG
0.200 Biomarker disease RGD [Effects of electroacupuncture intervention on blood lipid levels and expression of CD 40 L and MMP-9 in the coronary artery tissue in coronary heart disease rats]. 23819214 2013
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
0.050 GeneticVariation disease BEFREE With the recent identification of the largest number of individuals heterozygous for loss-of-function mutations in ABCA1 worldwide, population studies suggests that genetically low HDL cholesterol per se does not predict an increased risk of IHD, and thus questions the causality of isolated low levels of HDL cholesterol for the development of IHD. 19596329 2010
Entrez Id: 335
Gene Symbol: APOA1
APOA1
0.050 GeneticVariation disease BEFREE Wild-type apoA-I protein was compared to human variants that either are protective (R173C, Milano) or lead to increased risk for ischaemic heart disease (A164S). 29051568 2017
Entrez Id: 1827
Gene Symbol: RCAN1
RCAN1
0.010 AlteredExpression disease BEFREE Wild type (WT), Rcan1 KO, and Rcan1-Tg mice, with cardiomyocyte-specific overexpression of Rcan1, were subjected to 45min of myocardial ischemia followed by 24h of reperfusion. 24838101 2014
Entrez Id: 3091
Gene Symbol: HIF1A
HIF1A
0.300 Biomarker disease BEFREE Whole-genome array from intense light-exposed wild-type or Per2<sup>-/-</sup> mice and myocardial ischemia in endothelial-specific PER2-deficient mice uncover a critical role for intense light in maintaining endothelial barrier function via light-enhanced HIF1A transcription. 31390562 2019
Entrez Id: 8864
Gene Symbol: PER2
PER2
0.050 Biomarker disease BEFREE Whole-genome array from intense light-exposed wild-type or Per2<sup>-/-</sup> mice and myocardial ischemia in endothelial-specific PER2-deficient mice uncover a critical role for intense light in maintaining endothelial barrier function via light-enhanced HIF1A transcription. 31390562 2019
Entrez Id: 10578
Gene Symbol: GNLY
GNLY
0.010 Biomarker disease BEFREE While PM<sub>2.5</sub> concentration of lag2 and lag02 rose by 10 μg/m³, the ER of IHD mortality were 2.87% (95% CI: 0.71⁻5.07%) and 3.86% (95% CI: 1.17⁻6.63%), respectively. 30177663 2018
Entrez Id: 348
Gene Symbol: APOE
APOE
0.300 GeneticVariation disease BEFREE Whether plasma levels of apoE are associated with increased risk of dementia and ischemic heart disease, and whether these associations are independent of the APOE polymorphism and of lipids and lipoproteins has only recently been established. 28340945 2016
Entrez Id: 6678
Gene Symbol: SPARC
SPARC
0.310 Biomarker disease BEFREE Whereas the extracellular matrix protein Secreted Protein Acidic and Rich in Cysteine or SPARC has been implicated in hypertensive and ischemic heart disease by modulating collagen production and cross-linking, its role in cardiac inflammation and endothelial function is yet unknown. 29730504 2018
Entrez Id: 23410
Gene Symbol: SIRT3
SIRT3
0.050 Biomarker disease BEFREE Whereas the Sirt3-induced autophagy in different phases of myocardial ischemia-reperfusion has not been systematically illustrated. 30485429 2019
Entrez Id: 10454
Gene Symbol: TAB1
TAB1
0.010 GeneticVariation disease BEFREE Whereas ablating p38α or TAB1 resulted in early embryonal lethality, the TAB1-KI mice were viable and had no appreciable alteration in their lymphocyte repertoire or myocardial transcriptional profile; nonetheless, following in vivo regional myocardial ischemia, infarction volume was significantly reduced and the transphosphorylation of TAB1 was disabled. 30135318 2018
Entrez Id: 3569
Gene Symbol: IL6
IL6
0.390 GeneticVariation disease BEFREE When available studies were pooled into the meta-analysis, there was no significant association between IL-6 polymorphisms (-174G/C, -572G/C) and IHD/IS in any comparison model (CC vs GG, GC vs GG, dominant, and recessive models). 21536090 2011
Entrez Id: 3958
Gene Symbol: LGALS3
LGALS3
0.010 Biomarker disease BEFREE What is New: • The observed positive results of cardiac troponin I and high values of galectin-3 in sickle cell children during vaso-occlusive crisis are strong indicator of myocardial ischemia and ongoing cardiac fibrosis respectively. 30194527 2018
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
0.090 Biomarker disease BEFREE What is New: • The observed positive results of cardiac troponin I and high values of galectin-3 in sickle cell children during vaso-occlusive crisis are strong indicator of myocardial ischemia and ongoing cardiac fibrosis respectively. 30194527 2018
Entrez Id: 187
Gene Symbol: APLNR
APLNR
0.030 AlteredExpression disease BEFREE Western blotting and Real-time PCR were used to determine if APJ was expressed in the infant myocardium, if expression was influenced by the duration of myocardial ischemia and if any relationship existed between APJ expression and early post-operative outcome. 25184296 2014
Entrez Id: 7295
Gene Symbol: TXN
TXN
0.040 Biomarker disease BEFREE We will then discuss how Trx1 regulates the functions of its targets, thereby affecting the extent of myocardial injury caused by myocardial ischemia/reperfusion and the progression of heart failure. 27993729 2017
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.020 Biomarker disease BEFREE We will then discuss how Trx1 regulates the functions of its targets, thereby affecting the extent of myocardial injury caused by myocardial ischemia/reperfusion and the progression of heart failure. 27993729 2017
Entrez Id: 217
Gene Symbol: ALDH2
ALDH2
0.230 GeneticVariation disease BEFREE We used linear regression to assess the strength of the association of ALDH2 variants with alcohol use, whether ALDH2 variants were independently associated with socio-economic position or other potential confounders and whether associations of ALDH2 variants with cardiovascular risk factors (systolic and diastolic blood pressure, HDL- and LDL-cholesterol, fasting glucose), triglycerides, body mass index, self reported cardiovascular disease, self-reported ischaemic heart disease, cognitive function (delayed 10-word recall and Mini Mental State Examination score) and liver function (alanine transaminase and aspartate transaminase) were fully mediated by alcohol use. 23243119 2013
Entrez Id: 25813
Gene Symbol: SAMM50
SAMM50
0.010 GeneticVariation disease BEFREE We used instrumental variable analysis based on two single nucleotide polymorphism (SNPs) HSD17B13/MAPK10 (rs6834314) and PNPLA3/SAMM50 (rs738409) to assess the associations of ALT (U/L) with IHD, diabetes and other CVD risk factors in the Guangzhou Biobank Cohort Study (GBCS). 28007909 2017
Entrez Id: 80339
Gene Symbol: PNPLA3
PNPLA3
0.020 GeneticVariation disease BEFREE We used instrumental variable analysis based on two single nucleotide polymorphism (SNPs) HSD17B13/MAPK10 (rs6834314) and PNPLA3/SAMM50 (rs738409) to assess the associations of ALT (U/L) with IHD, diabetes and other CVD risk factors in the Guangzhou Biobank Cohort Study (GBCS). 28007909 2017
Entrez Id: 5602
Gene Symbol: MAPK10
MAPK10
0.010 GeneticVariation disease BEFREE We used instrumental variable analysis based on two single nucleotide polymorphism (SNPs) HSD17B13/MAPK10 (rs6834314) and PNPLA3/SAMM50 (rs738409) to assess the associations of ALT (U/L) with IHD, diabetes and other CVD risk factors in the Guangzhou Biobank Cohort Study (GBCS). 28007909 2017
Entrez Id: 345275
Gene Symbol: HSD17B13
HSD17B13
0.010 GeneticVariation disease BEFREE We used instrumental variable analysis based on two single nucleotide polymorphism (SNPs) HSD17B13/MAPK10 (rs6834314) and PNPLA3/SAMM50 (rs738409) to assess the associations of ALT (U/L) with IHD, diabetes and other CVD risk factors in the Guangzhou Biobank Cohort Study (GBCS). 28007909 2017
Entrez Id: 9365
Gene Symbol: KL
KL
0.020 GeneticVariation disease BEFREE We tested the hypothesis that the G-395A polymorphism of the klotho gene is associated with increased risk for 2 types of ischemic heart disease in Japanese. 16579981 2006
Entrez Id: 338
Gene Symbol: APOB
APOB
0.100 GeneticVariation disease BEFREE We tested the hypothesis that the APOB 7673C>T polymorphism (T2488T) is associated with variation in low-density lipoprotein (LDL) levels and with risk of ischemic heart disease (IHD), ischemic cerebrovascular disease (ICVD), and total mortality in the general population. 16030169 2005