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 |
---|---|---|---|---|---|
C0020538 | Hypertensive disease | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0740858 | Substance abuse problem | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0162871 | Aortic Aneurysm, Abdominal | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0236969 | Substance-Related Disorders | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
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 |
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Last updated: August 19, 2024