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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 |
|---|---|---|---|---|---|
| C0015397 | Disorder of eye | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0004106 | Astigmatism | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0025517 | Metabolic Diseases | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C4551686 | Malignant neoplasm of soft tissue | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0585442 | Osteosarcoma of bone | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C1335302 | Pancreatic Ductal Adenocarcinoma | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0011570 | Mental Depression | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C3161174 | Hemoglobin H Disease | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0035305 | Retinal Detachment | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C1851100 | LAURIN-SANDROW SYNDROME | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0020445 | Hypercholesterolemia, Familial | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0745103 | Hyperlipoproteinemia Type IIa | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0011581 | Depressive disorder | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0002418 | Amblyopia | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0008925 | Cleft Palate | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0007117 | Basal cell carcinoma | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0027651 | Neoplasms | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0023467 | Leukemia, Myelocytic, Acute | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C4303860 | Craniofacial ulnar renal syndrome | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0796032 | Malpuech facial clefting syndrome | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0431663 | Bilateral Cryptorchidism | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0024419 | Waldenstrom Macroglobulinemia | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0013336 | Dwarfism | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
