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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 |
|---|---|---|---|---|---|
| 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 |
| C1856127 | Bile acid synthesis defect, congenital, 2 | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0019158 | Hepatitis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0011849 | Diabetes Mellitus | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0000768 | Congenital Abnormality | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0019159 | Hepatitis A | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0392514 | Hereditary hemochromatosis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0029456 | Osteoporosis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0023895 | Liver diseases | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0024523 | Malabsorption Syndrome | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0027051 | Myocardial Infarction | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0008372 | Intrahepatic Cholestasis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0005779 | Blood Coagulation Disorders | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C2711227 | Steatohepatitis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
