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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 |
|---|---|---|---|---|---|
| C0025312 | Meningomyelocele | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C1833104 | DIABETES MELLITUS, PERMANENT NEONATAL | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0007102 | Malignant tumor of colon | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0015934 | Fetal Growth Retardation | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C1458155 | Mammary Neoplasms | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0268186 | Congenital glucose-galactose malabsorption | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0006826 | Malignant Neoplasms | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0085682 | Hypophosphatemia | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0007137 | Squamous cell carcinoma | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0015624 | Fanconi Syndrome | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0042769 | Virus Diseases | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| 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 |
