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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 |
|---|---|---|---|---|---|
| C0008350 | Cholelithiasis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1860787 | DOWN SYNDROME CRITICAL REGION | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1332986 | Childhood Osteosarcoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0010051 | Coronary Aneurysm | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0019187 | Hepatitis, Alcoholic | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0015397 | Disorder of eye | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0585442 | Osteosarcoma of bone | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1332979 | Childhood Lymphoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0020456 | Hyperglycemia | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0025267 | Multiple Endocrine Neoplasia Type 1 | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0007787 | Transient Ischemic Attack | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0340305 | Inferior Wall Myocardial Infarction | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1332206 | Adult Lymphoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0027051 | Myocardial Infarction | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C2239176 | Liver carcinoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0878544 | Cardiomyopathies | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1868683 | B-CELL MALIGNANCY, LOW-GRADE | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0949857 | Mitochondrial Respiratory Chain Deficiencies | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0006142 | Malignant neoplasm of breast | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
| C0020538 | Hypertensive disease | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
| C0014175 | Endometriosis | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
| C0027651 | Neoplasms | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
| C0029408 | Degenerative polyarthritis | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
| C0007114 | Malignant neoplasm of skin | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
| C0345904 | Malignant neoplasm of liver | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
