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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 |
|---|---|---|---|---|---|
| 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 |
| C0043346 | Xeroderma Pigmentosum | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0344315 | Depressed mood | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C2711227 | Steatohepatitis | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0026277 | Mixed Salivary Gland Tumor | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0027092 | Myopia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0007785 | Cerebral Infarction | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0026269 | Mitral Valve Stenosis | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0023787 | Lipodystrophy | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0004623 | Bacterial Infections | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
