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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 |
|---|---|---|---|---|---|
| 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 |
| C0009398 | Color vision defect | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0020757 | Ichthyoses | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0242383 | Age related macular degeneration | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0036572 | Seizures | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0456909 | Blindness | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0020620 | Hypohidrosis | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0265961 | Erythrokeratodermia variabilis | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C2239176 | Liver carcinoma | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C1838644 | Stargardt disease 3 | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0015397 | Disorder of eye | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C4282180 | Juvenile macular degeneration | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
