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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 |
|---|---|---|---|---|---|
| C3714756 | Intellectual Disability | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0011581 | Depressive disorder | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0023480 | Leukemia, Myelomonocytic, Chronic | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0008354 | Cholera | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0018784 | Sensorineural Hearing Loss (disorder) | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0085580 | Essential Hypertension | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0376359 | Gronblad-Strandberg Syndrome | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0022658 | Kidney Diseases | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0018818 | Ventricular Septal Defects | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0085669 | Acute leukemia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C1561643 | Chronic Kidney Diseases | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0042769 | Virus Diseases | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0026267 | Mitral Valve Prolapse Syndrome | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C1535939 | Pneumocystis jiroveci pneumonia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0002418 | Amblyopia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0030567 | Parkinson Disease | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0020433 | Hyperbilirubinemia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0948008 | Ischemic stroke | XYLB | 9942 | xylulokinase | O75191 |
