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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name ▼ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C1956346 | Coronary Artery Disease | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C1956346 | Coronary Artery Disease | LTC4S | 4056 | leukotriene C4 synthase | Q16873 |
| C1956346 | Coronary Artery Disease | LMAN1 | 3998 | lectin, mannose binding 1 | P49257 |
| C1956346 | Coronary Artery Disease | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
| C1956346 | Coronary Artery Disease | OXCT1 | 5019 | 3-oxoacid CoA-transferase 1 | P55809 |
| C1956346 | Coronary Artery Disease | PCYT1A | 5130 | phosphate cytidylyltransferase 1, choline, alpha | P49585 |
| C1956346 | Coronary Artery Disease | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C1956346 | Coronary Artery Disease | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C1956346 | Coronary Artery Disease | PKD1 | 5310 | polycystin 1, transient receptor potential channel interacting | P98161 |
| C1956346 | Coronary Artery Disease | PLA2G1B | 5319 | phospholipase A2 group IB | P04054 |
| C1956346 | Coronary Artery Disease | PLA2G5 | 5322 | phospholipase A2 group V | P39877 |
| C1956346 | Coronary Artery Disease | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C1956346 | Coronary Artery Disease | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C1956346 | Coronary Artery Disease | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C1956346 | Coronary Artery Disease | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1956346 | Coronary Artery Disease | PLA2G7 | 7941 | phospholipase A2 group VII | Q13093 |
| C1956346 | Coronary Artery Disease | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
| C0010054 | Coronary Arteriosclerosis | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C0010054 | Coronary Arteriosclerosis | FUT3 | 2525 | fucosyltransferase 3 (Lewis blood group) | P21217 |
| C0010054 | Coronary Arteriosclerosis | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
| C0010054 | Coronary Arteriosclerosis | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0010054 | Coronary Arteriosclerosis | GALNT2 | 2590 | polypeptide N-acetylgalactosaminyltransferase 2 | Q10471 |
| C0010054 | Coronary Arteriosclerosis | NDST4 | 64579 | N-deacetylase and N-sulfotransferase 4 | Q9H3R1 |
| C0010054 | Coronary Arteriosclerosis | ST8SIA4 | 7903 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 | Q92187 |
| C0010054 | Coronary Arteriosclerosis | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
