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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 |
|---|---|---|---|---|---|
| C0585442 | Osteosarcoma of bone | VNN2 | 8875 | vanin 2 | O95498 |
| C0033860 | Psoriasis | VNN2 | 8875 | vanin 2 | O95498 |
| C1621958 | Glioblastoma Multiforme | VNN2 | 8875 | vanin 2 | O95498 |
| C1306459 | Primary malignant neoplasm | VNN2 | 8875 | vanin 2 | O95498 |
| C0006826 | Malignant Neoplasms | VNN2 | 8875 | vanin 2 | O95498 |
| C0017636 | Glioblastoma | VNN2 | 8875 | vanin 2 | O95498 |
| C0015624 | Fanconi Syndrome | VNN2 | 8875 | vanin 2 | O95498 |
| C2931187 | Nephropathic cystinosis | VNN2 | 8875 | vanin 2 | O95498 |
| C0006142 | Malignant neoplasm of breast | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
| C0086132 | Depressive Symptoms | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
| C0684249 | Carcinoma of lung | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
| C0699790 | Colon Carcinoma | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
| C0431399 | Familial aplasia of the vermis | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
| C0007102 | Malignant tumor of colon | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
| C0026850 | Muscular Dystrophy | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
| C0002736 | Amyotrophic Lateral Sclerosis | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
| C0278878 | Adult Glioblastoma | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
| C0017636 | Glioblastoma | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
| C0036857 | Severe intellectual disability | ST3GAL5 | 8869 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Q9UNP4 |
| C0220756 | Niemann-Pick Disease, Type C | ST3GAL5 | 8869 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Q9UNP4 |
| C1869117 | Paroxysmal nonkinesigenic dyskinesia | ST3GAL5 | 8869 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Q9UNP4 |
| C0035372 | Rett Syndrome | ST3GAL5 | 8869 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Q9UNP4 |
| C0040021 | Thromboangiitis Obliterans | ST3GAL5 | 8869 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Q9UNP4 |
| C2239176 | Liver carcinoma | ST3GAL5 | 8869 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Q9UNP4 |
| C0027066 | Myoclonus | ST3GAL5 | 8869 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Q9UNP4 |
