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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 |
|---|---|---|---|---|---|
| C0917805 | Transient Cerebral Ischemia | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C0917805 | Transient Cerebral Ischemia | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0917805 | Transient Cerebral Ischemia | GPX3 | 2878 | glutathione peroxidase 3 | P22352 |
| C0917805 | Transient Cerebral Ischemia | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
| C0917805 | Transient Cerebral Ischemia | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C0917805 | Transient Cerebral Ischemia | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C0917805 | Transient Cerebral Ischemia | PLA2G7 | 7941 | phospholipase A2 group VII | Q13093 |
| C0342701 | Transcobalamin II deficiency | MMUT | 4594 | methylmalonyl-CoA mutase | P22033 |
| C0040592 | Trachoma | IL18R1 | 8809 | interleukin 18 receptor 1 | Q13478 |
| C0040583 | Tracheal Stenosis | IDUA | 3425 | alpha-L-iduronidase | P35475 |
| C0040583 | Tracheal Stenosis | EBP | 10682 | EBP cholestenol delta-isomerase | Q15125 |
| C0040580 | Tracheal Diseases | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0040580 | Tracheal Diseases | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0040580 | Tracheal Diseases | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0040580 | Tracheal Diseases | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
| C0040580 | Tracheal Diseases | DPEP3 | 64180 | dipeptidase 3 | Q9H4B8 |
| C0040580 | Tracheal Diseases | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
| C0040580 | Tracheal Diseases | VCAM1 | 7412 | vascular cell adhesion molecule 1 | P19320 |
| C0040580 | Tracheal Diseases | UGT2A1 | 10941 | UDP glucuronosyltransferase family 2 member A1 complex locus | Q9Y4X1 |
| C0040580 | Tracheal Diseases | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
| C0040580 | Tracheal Diseases | CEACAM6 | 4680 | CEA cell adhesion molecule 6 | P40199 |
| C0040580 | Tracheal Diseases | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0040560 | Toxoplasmosis, Congenital | ALOX12 | 239 | arachidonate 12-lipoxygenase, 12S type | P18054 |
| C0040558 | Toxoplasmosis | FUT3 | 2525 | fucosyltransferase 3 (Lewis blood group) | P21217 |
| C0040558 | Toxoplasmosis | FUT2 | 2524 | fucosyltransferase 2 | Q10981 |
