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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 ▲ |
|---|---|---|---|---|---|
| C0008925 | Cleft Palate | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0432242 | Desbuquois syndrome | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0158266 | Intervertebral Disc Degeneration | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0702166 | Acne | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0021775 | Intermittent Claudication | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0038586 | Substance Use Disorders | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0036439 | Scoliosis, unspecified | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0018818 | Ventricular Septal Defects | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0038580 | Substance Dependence | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0015934 | Fetal Growth Retardation | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C1319466 | Barber Say syndrome | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C0392476 | Epiphyseal dysplasia | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| 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 |
