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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 ▼ |
|---|---|---|---|---|---|
| C0279626 | Squamous cell carcinoma of esophagus | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0007682 | CNS disorder | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0039730 | Thalassemia | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0033860 | Psoriasis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0234533 | Generalized seizures | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0033578 | Prostatic Neoplasms | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0004096 | Asthma | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0010481 | Cushing Syndrome | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C4721555 | Autoimmune hepatitis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0241910 | Autoimmune Chronic Hepatitis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0151744 | Myocardial Ischemia | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0020179 | Huntington Disease | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0004106 | Astigmatism | MELTF | 4241 | melanotransferrin | P08582 |
| C0009402 | Colorectal Carcinoma | MELTF | 4241 | melanotransferrin | P08582 |
| C0025202 | melanoma | MELTF | 4241 | melanotransferrin | P08582 |
| C0027651 | Neoplasms | MELTF | 4241 | melanotransferrin | P08582 |
| C1332986 | Childhood Osteosarcoma | MELTF | 4241 | melanotransferrin | P08582 |
| C1306459 | Primary malignant neoplasm | MELTF | 4241 | melanotransferrin | P08582 |
| C0007097 | Carcinoma | MELTF | 4241 | melanotransferrin | P08582 |
| C0024623 | Malignant neoplasm of stomach | MELTF | 4241 | melanotransferrin | P08582 |
| C0006826 | Malignant Neoplasms | MELTF | 4241 | melanotransferrin | P08582 |
| C0002395 | Alzheimer's Disease | MELTF | 4241 | melanotransferrin | P08582 |
| C0007847 | Malignant tumor of cervix | MELTF | 4241 | melanotransferrin | P08582 |
| C0020459 | Hyperinsulinism | MELTF | 4241 | melanotransferrin | P08582 |
| C0585442 | Osteosarcoma of bone | MELTF | 4241 | melanotransferrin | P08582 |
