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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 |
|---|---|---|---|---|---|
| C0003850 | Arteriosclerosis | PTGIS | 5740 | prostaglandin I2 synthase | Q16647 |
| C0003850 | Arteriosclerosis | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0003850 | Arteriosclerosis | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C0003850 | Arteriosclerosis | PLA2G7 | 7941 | phospholipase A2 group VII | Q13093 |
| C0003850 | Arteriosclerosis | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0003850 | Arteriosclerosis | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
| C0852949 | Arteriopathic disease | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0852949 | Arteriopathic disease | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
| C0852949 | Arteriopathic disease | ARSA | 410 | arylsulfatase A | P15289 |
| C0852949 | Arteriopathic disease | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
| C0852949 | Arteriopathic disease | ACE | 1636 | angiotensin I converting enzyme | P12821 |
| C0852949 | Arteriopathic disease | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0852949 | Arteriopathic disease | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0852949 | Arteriopathic disease | SELE | 6401 | selectin E | P16581 |
| C0852949 | Arteriopathic disease | RENBP | 5973 | renin binding protein | P51606 |
| C0852949 | Arteriopathic disease | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
| C0852949 | Arteriopathic disease | GPX3 | 2878 | glutathione peroxidase 3 | P22352 |
| C0852949 | Arteriopathic disease | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
| C0852949 | Arteriopathic disease | PLA2G7 | 7941 | phospholipase A2 group VII | Q13093 |
| C1859727 | Arterial calcification of infancy | ENPP1 | 5167 | ectonucleotide pyrophosphatase/phosphodiesterase 1 | P22413 |
| C1859727 | Arterial calcification of infancy | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0003838 | Arterial Occlusive Diseases | IGF2R | 3482 | insulin like growth factor 2 receptor | P11717 |
| C0003838 | Arterial Occlusive Diseases | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
| C0003838 | Arterial Occlusive Diseases | STS | 412 | steroid sulfatase | P08842 |
| C0003838 | Arterial Occlusive Diseases | SELL | 6402 | selectin L | P14151 |
