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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 |
|---|---|---|---|---|---|
| C0006142 | Malignant neoplasm of breast | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0262655 | Recurrent urinary tract infection | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0011847 | Diabetes | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0678222 | Breast Carcinoma | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0017661 | IGA Glomerulonephritis | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0376358 | Malignant neoplasm of prostate | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| 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 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0011847 | Diabetes | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0268186 | Congenital glucose-galactose malabsorption | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
