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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 |
|---|---|---|---|---|---|
| C0003873 | Rheumatoid Arthritis | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
| C0282577 | Congenital Disorders of Glycosylation | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
| C0024623 | Malignant neoplasm of stomach | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
| C0426970 | Spastic Quadriplegia | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
| C0007222 | Cardiovascular Diseases | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
| C0010417 | Cryptorchidism | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0023434 | Chronic Lymphocytic Leukemia | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C2931011 | Congenital disorder of glycosylation, type 2G | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0235946 | Cerebral atrophy | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0002871 | Anemia | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0265342 | Cerebrocostomandibular Syndrome | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0015934 | Fetal Growth Retardation | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0376545 | Hematologic Neoplasms | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0040034 | Thrombocytopenia | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0031900 | Pierre Robin Syndrome | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0575158 | Kyphoscoliosis deformity of spine | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0006413 | Burkitt Lymphoma | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C1565489 | Renal Insufficiency | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0020295 | Hydronephrosis | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0848558 | Hypospadias | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0009081 | Congenital clubfoot | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C1384666 | hearing impairment | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C1842836 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C3203102 | Idiopathic pulmonary arterial hypertension | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C0036439 | Scoliosis, unspecified | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
