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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 |
|---|---|---|---|---|---|
| C2239176 | Liver carcinoma | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0338106 | Adenocarcinoma of colon | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0699790 | Colon Carcinoma | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0919267 | ovarian neoplasm | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0036631 | Seminoma | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0023903 | Liver neoplasms | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0279584 | Childhood B Acute Lymphoblastic Leukemia | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0017638 | Glioma | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0027819 | Neuroblastoma | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C4721610 | Carcinoma, Ovarian Epithelial | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C1800706 | Idiopathic Pulmonary Fibrosis | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0023467 | Leukemia, Myelocytic, Acute | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0400966 | Non-alcoholic Fatty Liver Disease | SLC2A8 | 29988 | solute carrier family 2 member 8 | Q9NY64 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | SLC2A8 | 29988 | solute carrier family 2 member 8 | Q9NY64 |
| C0026764 | Multiple Myeloma | SLC2A8 | 29988 | solute carrier family 2 member 8 | Q9NY64 |
| C0020676 | Hypothyroidism | SLC2A8 | 29988 | solute carrier family 2 member 8 | Q9NY64 |
| C0027651 | Neoplasms | SLC2A8 | 29988 | solute carrier family 2 member 8 | Q9NY64 |
| C1847593 | EPIPHYSEAL DYSPLASIA, MULTIPLE, 4 | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1850555 | De La Chapelle Dysplasia | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0265274 | Achondrogenesis, type IB (disorder) | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1384666 | hearing impairment | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1850554 | Atelosteogenesis type 2 | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0220726 | Diastrophic dysplasia | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0029422 | Osteochondrodysplasias | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
