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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 ▼ |
|---|---|---|---|---|---|
| C0007785 | Cerebral Infarction | FCN1 | 2219 | ficolin 1 | O00602 |
| C0004364 | Autoimmune Diseases | FCN1 | 2219 | ficolin 1 | O00602 |
| C0024143 | Lupus Nephritis | FCN1 | 2219 | ficolin 1 | O00602 |
| C0003864 | Arthritis | FCN1 | 2219 | ficolin 1 | O00602 |
| C0009402 | Colorectal Carcinoma | FCN1 | 2219 | ficolin 1 | O00602 |
| C0007786 | Brain Ischemia | FCN1 | 2219 | ficolin 1 | O00602 |
| C0035436 | Rheumatic Fever | FCN1 | 2219 | ficolin 1 | O00602 |
| C1956346 | Coronary Artery Disease | FCN1 | 2219 | ficolin 1 | O00602 |
| C0042384 | Vasculitis | FCN1 | 2219 | ficolin 1 | O00602 |
| C0007787 | Transient Ischemic Attack | FCN1 | 2219 | ficolin 1 | O00602 |
| C4082937 | Necrotizing enterocolitis in fetus OR newborn | FCN1 | 2219 | ficolin 1 | O00602 |
| C0948008 | Ischemic stroke | FCN1 | 2219 | ficolin 1 | O00602 |
| C3808739 | MYASTHENIC SYNDROME, CONGENITAL, 8 | AGRN | 375790 | agrin | O00468 |
| C0023467 | Leukemia, Myelocytic, Acute | AGRN | 375790 | agrin | O00468 |
| C0152013 | Adenocarcinoma of lung (disorder) | AGRN | 375790 | agrin | O00468 |
| C0028738 | Nystagmus | AGRN | 375790 | agrin | O00468 |
| C0238463 | Papillary thyroid carcinoma | AGRN | 375790 | agrin | O00468 |
| C0036572 | Seizures | AGRN | 375790 | agrin | O00468 |
| C0018784 | Sensorineural Hearing Loss (disorder) | AGRN | 375790 | agrin | O00468 |
| C0751883 | Congenital Myasthenic Syndromes, Postsynaptic | AGRN | 375790 | agrin | O00468 |
| C0751882 | Myasthenic Syndromes, Congenital | AGRN | 375790 | agrin | O00468 |
| C0002395 | Alzheimer's Disease | AGRN | 375790 | agrin | O00468 |
| C0026998 | Acute Myeloid Leukemia, M1 | AGRN | 375790 | agrin | O00468 |
| C0014877 | Esotropia | AGRN | 375790 | agrin | O00468 |
| C1306459 | Primary malignant neoplasm | AGRN | 375790 | agrin | O00468 |
