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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 ▼ |
|---|---|---|---|---|---|
| C0409974 | Lupus Erythematosus | EFNA2 | 1943 | ephrin A2 | O43921 |
| C0476089 | Endometrial Carcinoma | EFNA2 | 1943 | ephrin A2 | O43921 |
| C0024138 | Lupus Erythematosus, Discoid | EFNA2 | 1943 | ephrin A2 | O43921 |
| C0699791 | Stomach Carcinoma | EFNA2 | 1943 | ephrin A2 | O43921 |
| C0017636 | Glioblastoma | EFNA2 | 1943 | ephrin A2 | O43921 |
| C0346647 | Malignant neoplasm of pancreas | EFNA2 | 1943 | ephrin A2 | O43921 |
| C4048328 | cervical cancer | EFNA2 | 1943 | ephrin A2 | O43921 |
| C0006142 | Malignant neoplasm of breast | EFNA2 | 1943 | ephrin A2 | O43921 |
| C0023467 | Leukemia, Myelocytic, Acute | EFNA2 | 1943 | ephrin A2 | O43921 |
| C0017185 | Gastrointestinal Neoplasms | EFNA2 | 1943 | ephrin A2 | O43921 |
| C0376358 | Malignant neoplasm of prostate | EFNA2 | 1943 | ephrin A2 | O43921 |
| C1704272 | Benign Prostatic Hyperplasia | EFNA2 | 1943 | ephrin A2 | O43921 |
| C0086543 | Cataract | CHST1 | 8534 | carbohydrate sulfotransferase 1 | O43916 |
| C0029422 | Osteochondrodysplasias | CHST1 | 8534 | carbohydrate sulfotransferase 1 | O43916 |
| C0006142 | Malignant neoplasm of breast | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C0023467 | Leukemia, Myelocytic, Acute | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C0029454 | Osteopetrosis | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C0278996 | Malignant Head and Neck Neoplasm | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C0023890 | Liver Cirrhosis | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C0678222 | Breast Carcinoma | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C3714756 | Intellectual Disability | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C0149985 | Syphilis, secondary | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C0027651 | Neoplasms | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C0086647 | Mucopolysaccharidosis Type IIIA | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
| C0015306 | Hereditary Multiple Exostoses | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
