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 |
---|---|---|---|---|---|
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 |
C0011615 | Dermatitis, Atopic | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0262655 | Recurrent urinary tract infection | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0021400 | Influenza | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C1535939 | Pneumocystis jiroveci pneumonia | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0013595 | Eczema | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0153252 | Systemic candidiasis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0004623 | Bacterial Infections | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0021390 | Inflammatory Bowel Diseases | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0013274 | Patent ductus arteriosus | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C1510586 | Autism Spectrum Disorders | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0012813 | Diverticulitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0003873 | Rheumatoid Arthritis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0151744 | Myocardial Ischemia | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0009324 | Ulcerative Colitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0239946 | Fibrosis, Liver | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 19, 2024