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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 |
|---|---|---|---|---|---|
| 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 |
| C0085110 | Severe Combined Immunodeficiency | MELTF | 4241 | melanotransferrin | P08582 |
| C0206663 | Neuroectodermal Tumor, Primitive | MELTF | 4241 | melanotransferrin | P08582 |
| C0017638 | Glioma | MELTF | 4241 | melanotransferrin | P08582 |
| C0206633 | Angiomyolipoma | MELTF | 4241 | melanotransferrin | P08582 |
| C0152013 | Adenocarcinoma of lung (disorder) | MELTF | 4241 | melanotransferrin | P08582 |
| C0151779 | Cutaneous Melanoma | MELTF | 4241 | melanotransferrin | P08582 |
| C0206094 | Neuroectodermal Tumor, Melanotic | MELTF | 4241 | melanotransferrin | P08582 |
| C4048328 | cervical cancer | MELTF | 4241 | melanotransferrin | P08582 |
| C0032460 | Polycystic Ovary Syndrome | MELTF | 4241 | melanotransferrin | P08582 |
| C0699791 | Stomach Carcinoma | MELTF | 4241 | melanotransferrin | P08582 |
| C0029463 | Osteosarcoma | MELTF | 4241 | melanotransferrin | P08582 |
| C0392475 | Roberts-SC phocomelia syndrome | MELTF | 4241 | melanotransferrin | P08582 |
| C1853137 | BRACHYDACTYLY-SYNDACTYLY SYNDROME | MBOAT1 | 154141 | membrane bound O-acyltransferase domain containing 1 | Q6ZNC8 |
| C0008370 | Cholestasis | MBOAT1 | 154141 | membrane bound O-acyltransferase domain containing 1 | Q6ZNC8 |
| C1527231 | Adrenomyeloneuropathy | MBOAT2 | 129642 | membrane bound O-acyltransferase domain containing 2 | Q6ZWT7 |
| C0400966 | Non-alcoholic Fatty Liver Disease | MBOAT7 | 79143 | membrane bound O-acyltransferase domain containing 7 | Q96N66 |
| C0019196 | Hepatitis C | MBOAT7 | 79143 | membrane bound O-acyltransferase domain containing 7 | Q96N66 |
| C0019163 | Hepatitis B | MBOAT7 | 79143 | membrane bound O-acyltransferase domain containing 7 | Q96N66 |
| C1510586 | Autism Spectrum Disorders | MBOAT7 | 79143 | membrane bound O-acyltransferase domain containing 7 | Q96N66 |
| C2239176 | Liver carcinoma | MBOAT7 | 79143 | membrane bound O-acyltransferase domain containing 7 | Q96N66 |
