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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 |
|---|---|---|---|---|---|
| C1275808 | Congenital central hypoventilation | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0018802 | Congestive heart failure | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0020538 | Hypertensive disease | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0022578 | Keratoconus | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0003504 | Aortic Valve Insufficiency | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0004096 | Asthma | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0026654 | Moyamoya Disease | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C1704436 | Peripheral Arterial Diseases | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C4721509 | Usual Interstitial Pneumonia | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C1442965 | Avascular necrosis of the capital femoral epiphysis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0035222 | Respiratory Distress Syndrome, Adult | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0678222 | Breast Carcinoma | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0011849 | Diabetes Mellitus | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0027051 | Myocardial Infarction | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0007120 | Bronchioloalveolar Adenocarcinoma | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0023234 | Legg-Calve-Perthes Disease | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0264490 | Acute respiratory failure | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0008479 | Chondrosarcoma | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C3714756 | Intellectual Disability | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0011847 | Diabetes | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0011633 | Dermatomyositis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0027092 | Myopia | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0007193 | Cardiomyopathy, Dilated | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C3812396 | Chronic idiopathic pulmonary fibrosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0002940 | Aneurysm | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
