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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 |
|---|---|---|---|---|---|
| C0026946 | Mycoses | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0041296 | Tuberculosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C1262117 | Fungal keratitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0037299 | Skin Ulcer | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0345904 | Malignant neoplasm of liver | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0235974 | Pancreatic carcinoma | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0004030 | Aspergillosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0021364 | Male infertility | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0033860 | Psoriasis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0036572 | Seizures | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0085859 | Polyglandular Type I Autoimmune Syndrome | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0013371 | Shigella Infections | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0007971 | Cheilitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0024143 | Lupus Nephritis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0008373 | Cholesteatoma | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0002726 | Amyloidosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0004096 | Asthma | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0022283 | Incontinentia Pigmenti Achromians | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0032285 | Pneumonia | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0003864 | Arthritis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0015230 | Exanthema | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0023467 | Leukemia, Myelocytic, Acute | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0029408 | Degenerative polyarthritis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0004153 | Atherosclerosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
