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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 |
|---|---|---|---|---|---|
| C0020428 | Hyperaldosteronism | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0271650 | Impaired glucose tolerance | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0007222 | Cardiovascular Diseases | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C3714636 | Pneumonitis | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0007785 | Cerebral Infarction | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0678222 | Breast Carcinoma | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0338508 | Optic Atrophy 1 | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0017658 | Glomerulonephritis | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0007194 | Hypertrophic Cardiomyopathy | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0023283 | Leishmaniasis, Cutaneous | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0004153 | Atherosclerosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0011849 | Diabetes Mellitus | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0041296 | Tuberculosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0004238 | Atrial Fibrillation | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0011847 | Diabetes | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0041327 | Tuberculosis, Pulmonary | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0678222 | Breast Carcinoma | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0010346 | Crohn Disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0029408 | Degenerative polyarthritis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0236970 | Alcohol-Induced Disorders | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0039585 | Androgen-Insensitivity Syndrome | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0700095 | Central neuroblastoma | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0020179 | Huntington Disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C4225234 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0243026 | Sepsis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
