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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 |
|---|---|---|---|---|---|
| C0004763 | Barrett Esophagus | MICA | 100507436 | MHC class I polypeptide-related sequence A | Q29983 |
| C0004763 | Barrett Esophagus | FASN | 2194 | fatty acid synthase | P49327 |
| C0004763 | Barrett Esophagus | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0004763 | Barrett Esophagus | GPX3 | 2878 | glutathione peroxidase 3 | P22352 |
| C0004763 | Barrett Esophagus | GPX2 | 2877 | glutathione peroxidase 2 | P18283 |
| C0004763 | Barrett Esophagus | CEACAM6 | 4680 | CEA cell adhesion molecule 6 | P40199 |
| C0004763 | Barrett Esophagus | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C0004763 | Barrett Esophagus | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0004763 | Barrett Esophagus | GOLPH3 | 64083 | golgi phosphoprotein 3 | Q9H4A6 |
| C0004763 | Barrett Esophagus | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C1332460 | Barrett's Adenocarcinoma | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0004775 | Bartter Disease | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C0004775 | Bartter Disease | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0004775 | Bartter Disease | HSD11B2 | 3291 | hydroxysteroid 11-beta dehydrogenase 2 | P80365 |
| C0004775 | Bartter Disease | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0751676 | Basal Cell Cancer | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0751676 | Basal Cell Cancer | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0206710 | Basal Cell Neoplasm | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0206710 | Basal Cell Neoplasm | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C0206710 | Basal Cell Neoplasm | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0004779 | Basal Cell Nevus Syndrome | GLB1 | 2720 | galactosidase beta 1 | P16278 |
| C0004779 | Basal Cell Nevus Syndrome | HPSE | 10855 | heparanase | Q9Y251 |
| C0004779 | Basal Cell Nevus Syndrome | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
| C0004779 | Basal Cell Nevus Syndrome | SLC2A3 | 6515 | solute carrier family 2 member 3 | P11169 |
| C0004779 | Basal Cell Nevus Syndrome | GPC3 | 2719 | glypican 3 | P51654 |
