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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 |
|---|---|---|---|---|---|
| C0028945 | oligodendroglioma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C3714756 | Intellectual Disability | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0264766 | Rheumatic mitral stenosis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0014173 | Endometrial Hyperplasia | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1175175 | Severe Acute Respiratory Syndrome | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0033578 | Prostatic Neoplasms | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0021390 | Inflammatory Bowel Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1332629 | Breast Fibrocystic Change, Proliferative Type | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0699791 | Stomach Carcinoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0524620 | Metabolic Syndrome X | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0038013 | Ankylosing spondylitis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0400966 | Non-alcoholic Fatty Liver Disease | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0025517 | Metabolic Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0007222 | Cardiovascular Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| 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 |
