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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 |
|---|---|---|---|---|---|
| C1449563 | Cardiomyopathy, Familial Idiopathic | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1832229 | Rieger syndrome 2 (disorder) | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0155686 | Acute myocarditis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0947622 | Cholecystolithiasis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0002965 | Angina, Unstable | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0677886 | Epithelial ovarian cancer | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0035309 | Retinal Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1704436 | Peripheral Arterial Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0025149 | Medulloblastoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0023434 | Chronic Lymphocytic Leukemia | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0025362 | Mental Retardation | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0595989 | Carcinoma of larynx | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0026269 | Mitral Valve Stenosis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0024809 | Marijuana Abuse | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0007102 | Malignant tumor of colon | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0039685 | Tetralogy of Fallot | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0701818 | Choledocholithiasis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0015306 | Hereditary Multiple Exostoses | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0018801 | Heart failure | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0009402 | Colorectal Carcinoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0007124 | Noninfiltrating Intraductal Carcinoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0032460 | Polycystic Ovary Syndrome | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0277528 | Traveler's diarrhea | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0919267 | ovarian neoplasm | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0010068 | Coronary heart disease | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
