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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 |
|---|---|---|---|---|---|
| C0014474 | Ependymoma | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0007131 | Non-Small Cell Lung Carcinoma | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0376358 | Malignant neoplasm of prostate | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0024117 | Chronic Obstructive Airway Disease | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0027947 | Neutropenia | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0220668 | Congenital contractural arachnodactyly | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0010346 | Crohn Disease | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0700095 | Central neuroblastoma | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C1332206 | Adult Lymphoma | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0001418 | Adenocarcinoma | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0699885 | Carcinoma of bladder | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0024299 | Lymphoma | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0678222 | Breast Carcinoma | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C1332979 | Childhood Lymphoma | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C1306759 | Eosinophilic disorder | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C0006142 | Malignant neoplasm of breast | TMTC4 | 84899 | transmembrane O-mannosyltransferase targeting cadherins 4 | Q5T4D3 |
| C1837461 | SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 | TMTC4 | 84899 | transmembrane O-mannosyltransferase targeting cadherins 4 | Q5T4D3 |
| C1531647 | Cerebral ventriculomegaly | TMTC3 | 160418 | transmembrane O-mannosyltransferase targeting cadherins 3 | Q6ZXV5 |
| C0027947 | Neutropenia | TMTC3 | 160418 | transmembrane O-mannosyltransferase targeting cadherins 3 | Q6ZXV5 |
| C0036572 | Seizures | TMTC3 | 160418 | transmembrane O-mannosyltransferase targeting cadherins 3 | Q6ZXV5 |
| C0027092 | Myopia | TMTC3 | 160418 | transmembrane O-mannosyltransferase targeting cadherins 3 | Q6ZXV5 |
| C0266483 | Pachygyria | TMTC3 | 160418 | transmembrane O-mannosyltransferase targeting cadherins 3 | Q6ZXV5 |
| C3714756 | Intellectual Disability | TMTC3 | 160418 | transmembrane O-mannosyltransferase targeting cadherins 3 | Q6ZXV5 |
| C0014544 | Epilepsy | TMTC3 | 160418 | transmembrane O-mannosyltransferase targeting cadherins 3 | Q6ZXV5 |
| C0003504 | Aortic Valve Insufficiency | TMTC3 | 160418 | transmembrane O-mannosyltransferase targeting cadherins 3 | Q6ZXV5 |
