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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 |
|---|---|---|---|---|---|
| C0021828 | Intestinal Atresia | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0085207 | Gestational Diabetes | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0020621 | Hypokalemia | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0699790 | Colon Carcinoma | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0341703 | Adult Fanconi syndrome | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0242363 | Islet Cell Tumor | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0016952 | Galactosemias | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0013595 | Eczema | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0524620 | Metabolic Syndrome X | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C1306459 | Primary malignant neoplasm | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0271708 | Fasting Hypoglycemia | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0011615 | Dermatitis, Atopic | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0001122 | Acidosis | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0007134 | Renal Cell Carcinoma | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0079731 | B-Cell Lymphomas | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0017980 | Glycosuria, Renal | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C3245525 | Familial renal glucosuria | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0376358 | Malignant neoplasm of prostate | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0011847 | Diabetes | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0027651 | Neoplasms | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0020676 | Hypothyroidism | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0002726 | Amyloidosis | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C1956346 | Coronary Artery Disease | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0026764 | Multiple Myeloma | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
