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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 |
|---|---|---|---|---|---|
| C1306459 | Primary malignant neoplasm | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0011644 | Scleroderma | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0002982 | Angioid Streaks | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0029456 | Osteoporosis | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0023895 | Liver diseases | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0028326 | Noonan Syndrome | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0035305 | Retinal Detachment | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0026010 | Microphthalmos | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0019163 | Hepatitis B | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0033847 | Pseudoxanthoma Elasticum | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0007196 | Restrictive cardiomyopathy | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0040034 | Thrombocytopenia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0027651 | Neoplasms | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0086543 | Cataract | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C3279392 | PSEUDOXANTHOMA ELASTICUM, MODIFIER OF SEVERITY OF | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0155626 | Acute myocardial infarction | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C1867450 | Pseudoxanthoma Elasticum, Incomplete | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0030354 | Papilloma | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C1565489 | Renal Insufficiency | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0016202 | Flatfoot | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0018802 | Congestive heart failure | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0036421 | Systemic Scleroderma | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0020538 | Hypertensive disease | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0004135 | Ataxia Telangiectasia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
