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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 |
|---|---|---|---|---|---|
| C0039101 | synovial sarcoma | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C1850889 | MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0020615 | Hypoglycemia | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0686353 | Muscular Dystrophies, Limb-Girdle | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0041349 | Nephritis, Tubulointerstitial | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C4551858 | Vesicoureteral Reflux 1 | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0020505 | Hyperphagia | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0005745 | Blepharoptosis | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0085580 | Essential Hypertension | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C1857389 | Cystinuria, Type B | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C1565489 | Renal Insufficiency | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0024796 | Marfan Syndrome | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0020538 | Hypertensive disease | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0030319 | Panic Disorder | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0011849 | Diabetes Mellitus | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0001125 | Acidosis, Lactic | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0004153 | Atherosclerosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0011849 | Diabetes Mellitus | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0041296 | Tuberculosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0004238 | Atrial Fibrillation | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0011847 | Diabetes | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0041327 | Tuberculosis, Pulmonary | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0678222 | Breast Carcinoma | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0010346 | Crohn Disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0029408 | Degenerative polyarthritis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
