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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 |
|---|---|---|---|---|---|
| C0040100 | Thymoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0220702 | SCHIZOPHRENIA 1 (disorder) | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1140680 | Malignant neoplasm of ovary | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0002736 | Amyotrophic Lateral Sclerosis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0024623 | Malignant neoplasm of stomach | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0278876 | Adult Medulloblastoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0018799 | Heart Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0023055 | Laryngeal neoplasm | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0086565 | Liver Dysfunction | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0013336 | Dwarfism | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0278510 | Childhood Medulloblastoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0022658 | Kidney Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0338106 | Adenocarcinoma of colon | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0029463 | Osteosarcoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0014175 | Endometriosis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0023895 | Liver diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0024299 | Lymphoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C3203102 | Idiopathic pulmonary arterial hypertension | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0007194 | Hypertrophic Cardiomyopathy | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0279583 | Childhood T Acute Lymphoblastic Leukemia | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0235480 | Paroxysmal atrial fibrillation | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0003493 | Aortic Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| 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 |
