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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 |
|---|---|---|---|---|---|
| C0007113 | Rectal Carcinoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0007102 | Malignant tumor of colon | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0006826 | Malignant Neoplasms | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0014474 | Ependymoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0278876 | Adult Medulloblastoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C1306459 | Primary malignant neoplasm | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0007114 | Malignant neoplasm of skin | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0026764 | Multiple Myeloma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0699790 | Colon Carcinoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0027651 | Neoplasms | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0740345 | Germ Cell Cancer | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0346647 | Malignant neoplasm of pancreas | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0019163 | Hepatitis B | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0006142 | Malignant neoplasm of breast | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0678222 | Breast Carcinoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0235974 | Pancreatic carcinoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0013421 | Dystonia | TECR | 9524 | trans-2,3-enoyl-CoA reductase | Q9NZ01 |
| C0000768 | Congenital Abnormality | TECR | 9524 | trans-2,3-enoyl-CoA reductase | Q9NZ01 |
| C0025362 | Mental Retardation | TECR | 9524 | trans-2,3-enoyl-CoA reductase | Q9NZ01 |
| C0235946 | Cerebral atrophy | TECR | 9524 | trans-2,3-enoyl-CoA reductase | Q9NZ01 |
| C0038273 | Stereotypic Movement Disorder | TECR | 9524 | trans-2,3-enoyl-CoA reductase | Q9NZ01 |
| C1527366 | Salaam Seizures | TECR | 9524 | trans-2,3-enoyl-CoA reductase | Q9NZ01 |
| C3714756 | Intellectual Disability | TECR | 9524 | trans-2,3-enoyl-CoA reductase | Q9NZ01 |
| C0234533 | Generalized seizures | TECR | 9524 | trans-2,3-enoyl-CoA reductase | Q9NZ01 |
| C3151462 | MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14 | TECR | 9524 | trans-2,3-enoyl-CoA reductase | Q9NZ01 |
