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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 |
|---|---|---|---|---|---|
| C0155626 | Acute myocardial infarction | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0036421 | Systemic Scleroderma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0027651 | Neoplasms | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C4721610 | Carcinoma, Ovarian Epithelial | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0020501 | Primary Hyperoxaluria | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0339573 | Glaucoma, Primary Open Angle | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0020538 | Hypertensive disease | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0038454 | Cerebrovascular accident | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0376358 | Malignant neoplasm of prostate | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0410173 | Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder) | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0600139 | Prostate carcinoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0678222 | Breast Carcinoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0242379 | Malignant neoplasm of lung | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0006118 | Brain Neoplasms | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0024796 | Marfan Syndrome | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0948008 | Ischemic stroke | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0007103 | Malignant neoplasm of endometrium | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0392514 | Hereditary hemochromatosis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0010674 | Cystic Fibrosis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1168401 | Squamous cell carcinoma of the head and neck | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0012236 | DiGeorge Syndrome | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1956346 | Coronary Artery Disease | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0751396 | Well Differentiated Oligodendroglioma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0040100 | Thymoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
