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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 |
|---|---|---|---|---|---|
| C0009782 | Connective Tissue Diseases | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C1458155 | Mammary Neoplasms | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0027059 | Myocarditis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0007194 | Hypertrophic Cardiomyopathy | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0600260 | Lung Diseases, Obstructive | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0034194 | Pyloric Stenosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0003486 | Aortic Aneurysm | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C1306503 | Congenital exomphalos | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0085096 | Peripheral Vascular Diseases | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0038379 | Strabismus | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0005744 | Blepharophimosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0264408 | Childhood asthma | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C1800706 | Idiopathic Pulmonary Fibrosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0010495 | Cutis Laxa | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0034067 | Pulmonary Emphysema | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0036439 | Scoliosis, unspecified | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| 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 |
| C0006142 | Malignant neoplasm of breast | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
