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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 ▼ |
|---|---|---|---|---|---|
| C0024623 | Malignant neoplasm of stomach | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0085584 | Encephalopathies | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0009402 | Colorectal Carcinoma | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0279985 | Childhood Alveolar Soft Part Sarcoma | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0152205 | Alternating esotropia | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0010964 | Dandy-Walker Syndrome | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C1531647 | Cerebral ventriculomegaly | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0036439 | Scoliosis, unspecified | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| C0027066 | Myoclonus | COG8 | 84342 | component of oligomeric golgi complex 8 | Q96MW5 |
| 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 |
| C0014060 | Encephalitis, St. Louis | GLT1D1 | 144423 | glycosyltransferase 1 domain containing 1 | Q96MS3 |
| C0010068 | Coronary heart disease | GLT1D1 | 144423 | glycosyltransferase 1 domain containing 1 | Q96MS3 |
| C0004096 | Asthma | GLT1D1 | 144423 | glycosyltransferase 1 domain containing 1 | Q96MS3 |
| C0152013 | Adenocarcinoma of lung (disorder) | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C0024623 | Malignant neoplasm of stomach | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C3714756 | Intellectual Disability | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C0029408 | Degenerative polyarthritis | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C0027092 | Myopia | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C1800706 | Idiopathic Pulmonary Fibrosis | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
