Table 1.
Name | Gene ID | Link to Atherosclerosis | Normal Function | Identification (Organism, Method) | Reference |
---|---|---|---|---|---|
ALOX5AP | 241 | Genetic variants are potentially contributed to the higher coronary heart disease risk | Part of leukotriene biosynthesis pathway | Human, haplotype association study | [22] |
MEF2A | 4205 | MEF2A signaling pathway is involved in pathogenesis of familial CAD and MI | Myocyte-specific transcription factor | Human, linkage study | [17] |
Alox5 | 11689 | homozygote 5LO null mice develop smaller atherosclerotic lesions | Part of leukotriene biosynthesis pathway | Mouse, linkage study | [18] |
Tnfsf4 | 22164 | blocking the OX-40/OX40L interaction reduced atherogenesis | OX40 ligand | Mouse, linkage study | [19] |
LTA | 4049 | Genetic variants are potentially contributed to the higher MI risk | Lymphocyte cytokine | Human, GWAS | [20] |
PSMA6 | 5687 | PSMA6 rs_1048990 polymorphism may contribute to MI susceptibility in type 2 diabetes | - | Human, GWAS | [23] |
CAD: coronary artery disease; MI: myocardial infarction; GWAS: genome-wide association study.