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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 |
|---|---|---|---|---|---|
| C3714756 | Intellectual Disability | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0025958 | Microcephaly | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0546837 | Malignant neoplasm of esophagus | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C4317295 | Congenital disorder of glycosylation type 1s | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0038220 | Status Epilepticus | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0206657 | Alveolar Soft Part Sarcoma | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C2239176 | Liver carcinoma | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0013336 | Dwarfism | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0235946 | Cerebral atrophy | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0282577 | Congenital Disorders of Glycosylation | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0017168 | Gastroesophageal reflux disease | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0020295 | Hydronephrosis | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0241005 | Creatine phosphokinase serum increased | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0020615 | Hypoglycemia | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C2931010 | Congenital disorder of glycosylation type 2E | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0079154 | Congenital Nonbullous Ichthyosiform Erythroderma | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C1384666 | hearing impairment | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0007194 | Hypertrophic Cardiomyopathy | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0020555 | Hypertrichosis | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0018798 | Congenital Heart Defects | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0018802 | Congestive heart failure | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0015934 | Fetal Growth Retardation | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0025958 | Microcephaly | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0005697 | Neurogenic Urinary Bladder | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0282577 | Congenital Disorders of Glycosylation | COG6 | 57511 | component of oligomeric golgi complex 6 | Q9Y2V7 |
