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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 ▲ |
|---|---|---|---|---|---|
| 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 |
| C0016202 | Flatfoot | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0019572 | Hirsutism | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0029408 | Degenerative polyarthritis | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0026277 | Mixed Salivary Gland Tumor | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0020608 | Hypodontia | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0007196 | Restrictive cardiomyopathy | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0015300 | Exophthalmos | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0038454 | Cerebrovascular accident | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0003469 | Anxiety Disorders | LYPD6 | 130574 | LY6/PLAUR domain containing 6 | Q86Y78 |
