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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 |
|---|---|---|---|---|---|
| C1858725 | NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM, FAMILIAL ISOLATED, AUTOSOMAL DOMINANT 1 | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0010278 | Craniosynostosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0021390 | Inflammatory Bowel Diseases | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0023418 | leukemia | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0036572 | Seizures | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0003850 | Arteriosclerosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0023264 | Leigh Disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0006142 | Malignant neoplasm of breast | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| 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 |
| C0025517 | Metabolic Diseases | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0018801 | Heart failure | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0020456 | Hyperglycemia | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0338106 | Adenocarcinoma of colon | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0006142 | Malignant neoplasm of breast | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0020615 | Hypoglycemia | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0243026 | Sepsis | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0151744 | Myocardial Ischemia | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0011849 | Diabetes Mellitus | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C1306459 | Primary malignant neoplasm | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0020538 | Hypertensive disease | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0027651 | Neoplasms | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0878544 | Cardiomyopathies | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
