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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 |
|---|---|---|---|---|---|
| C0008924 | Cleft upper lip | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0026764 | Multiple Myeloma | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0036439 | Scoliosis, unspecified | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C1378511 | Undifferentiated leukemia | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0005745 | Blepharoptosis | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0006826 | Malignant Neoplasms | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C1306503 | Congenital exomphalos | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0206710 | Basal Cell Neoplasm | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0158761 | Radioulnar Synostosis | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0023434 | Chronic Lymphocytic Leukemia | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0023449 | Acute lymphocytic leukemia | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C3463824 | MYELODYSPLASTIC SYNDROME | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0280141 | Acute Undifferentiated Leukemia | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C3714756 | Intellectual Disability | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C1384666 | hearing impairment | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0751676 | Basal Cell Cancer | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0004238 | Atrial Fibrillation | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0409959 | Osteoarthritis, Knee | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0013336 | Dwarfism | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C4707243 | Familial thoracic aortic aneurysm and aortic dissection | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0026760 | Multiple Epiphyseal Dysplasia | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0025149 | Medulloblastoma | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C2020284 | Stickler syndrome, type 1 | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0002312 | alpha-Thalassemia | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0278510 | Childhood Medulloblastoma | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
