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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 |
|---|---|---|---|---|---|
| C0013264 | Muscular Dystrophy, Duchenne | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0013146 | Drug abuse | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C3714756 | Intellectual Disability | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0026267 | Mitral Valve Prolapse Syndrome | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0242383 | Age related macular degeneration | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0473583 | Nevus elasticus | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0020678 | Hypotrichosis | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0025958 | Microcephaly | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0013170 | Drug habituation | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C1857941 | Brooke-Spiegler syndrome | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0023467 | Leukemia, Myelocytic, Acute | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0029422 | Osteochondrodysplasias | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C1510472 | Drug Dependence | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0158761 | Radioulnar Synostosis | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0004114 | Astrocytoma | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C1565489 | Renal Insufficiency | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0376359 | Gronblad-Strandberg Syndrome | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0017601 | Glaucoma | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0271561 | Somatotropin deficiency | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0013336 | Dwarfism | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0005129 | Bernard-Soulier Syndrome | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0544755 | Genu varum | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0027092 | Myopia | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0026269 | Mitral Valve Stenosis | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
