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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 ▼ |
|---|---|---|---|---|---|
| C0028738 | Nystagmus | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0027765 | nervous system disorder | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0151744 | Myocardial Ischemia | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0684249 | Carcinoma of lung | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C1306459 | Primary malignant neoplasm | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0206708 | Cervical Intraepithelial Neoplasia | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0006142 | Malignant neoplasm of breast | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0038379 | Strabismus | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0006118 | Brain Neoplasms | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0236773 | Depressed bipolar I disorder | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0520966 | Abnormal coordination | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0024776 | Maple Syrup Urine Disease | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0342642 | Autosomal dominant hypophosphatemic rickets | GALNT8 | 26290 | polypeptide N-acetylgalactosaminyltransferase 8 | Q9NY28 |
| C0025517 | Metabolic Diseases | GALNT8 | 26290 | polypeptide N-acetylgalactosaminyltransferase 8 | Q9NY28 |
| C0019196 | Hepatitis C | GALNT8 | 26290 | polypeptide N-acetylgalactosaminyltransferase 8 | Q9NY28 |
| C0011311 | Dengue Fever | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
| C0008373 | Cholesteatoma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
| C0029463 | Osteosarcoma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
| C0019100 | Severe Dengue | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
| C0278878 | Adult Glioblastoma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
| C0017636 | Glioblastoma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
| C0585442 | Osteosarcoma of bone | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
| C0017638 | Glioma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
| C0032302 | Mycoplasma pneumonia | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
| C0003850 | Arteriosclerosis | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
