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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 | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
| C1956346 | Coronary Artery Disease | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
| C1956346 | Coronary Artery Disease | CYP4A11 | 1579 | cytochrome P450 family 4 subfamily A member 11 | Q02928 |
| C1956346 | Coronary Artery Disease | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C1956346 | Coronary Artery Disease | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
| C1956346 | Coronary Artery Disease | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
| C1956346 | Coronary Artery Disease | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
| C1956346 | Coronary Artery Disease | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
| C1956346 | Coronary Artery Disease | EPHX2 | 2053 | epoxide hydrolase 2 | P34913 |
| C1956346 | Coronary Artery Disease | EFNA5 | 1946 | ephrin A5 | P52803 |
| C1956346 | Coronary Artery Disease | ALDH1B1 | 219 | aldehyde dehydrogenase 1 family member B1 | P30837 |
| C1956346 | Coronary Artery Disease | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
| C1956346 | Coronary Artery Disease | ALOX5 | 240 | arachidonate 5-lipoxygenase | P09917 |
| C1956346 | Coronary Artery Disease | ALOX15 | 246 | arachidonate 15-lipoxygenase | P16050 |
| C1956346 | Coronary Artery Disease | GPX3 | 2878 | glutathione peroxidase 3 | P22352 |
| C1956346 | Coronary Artery Disease | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
| 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 |
