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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 |
|---|---|---|---|---|---|
| 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 |
| C0013170 | Drug habituation | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0026769 | Multiple Sclerosis | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0013146 | Drug abuse | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0524620 | Metabolic Syndrome X | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0740858 | Substance abuse problem | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0038580 | Substance Dependence | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0026848 | Myopathy | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0038586 | Substance Use Disorders | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0003850 | Arteriosclerosis | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0013222 | Drug Use Disorders | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
