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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 |
|---|---|---|---|---|---|
| C0678222 | Breast Carcinoma | AGK | 55750 | acylglycerol kinase | Q53H12 |
| C0878544 | Cardiomyopathies | AGK | 55750 | acylglycerol kinase | Q53H12 |
| C0017601 | Glaucoma | AGK | 55750 | acylglycerol kinase | Q53H12 |
| C0010036 | Corneal dystrophy | AGK | 55750 | acylglycerol kinase | Q53H12 |
| C2931822 | Nasopharyngeal carcinoma | AGK | 55750 | acylglycerol kinase | Q53H12 |
| C0027651 | Neoplasms | OGDHL | 55753 | oxoglutarate dehydrogenase like | Q9ULD0 |
| C0235974 | Pancreatic carcinoma | OGDHL | 55753 | oxoglutarate dehydrogenase like | Q9ULD0 |
| C1306459 | Primary malignant neoplasm | OGDHL | 55753 | oxoglutarate dehydrogenase like | Q9ULD0 |
| C0002395 | Alzheimer's Disease | OGDHL | 55753 | oxoglutarate dehydrogenase like | Q9ULD0 |
| C0006826 | Malignant Neoplasms | OGDHL | 55753 | oxoglutarate dehydrogenase like | Q9ULD0 |
| C0006142 | Malignant neoplasm of breast | OGDHL | 55753 | oxoglutarate dehydrogenase like | Q9ULD0 |
| C0009402 | Colorectal Carcinoma | OGDHL | 55753 | oxoglutarate dehydrogenase like | Q9ULD0 |
| C0341106 | Eosinophilic esophagitis | OGDHL | 55753 | oxoglutarate dehydrogenase like | Q9ULD0 |
| C0345904 | Malignant neoplasm of liver | OGDHL | 55753 | oxoglutarate dehydrogenase like | Q9ULD0 |
| C0006826 | Malignant Neoplasms | UGGT2 | 55757 | UDP-glucose glycoprotein glucosyltransferase 2 | Q9NYU1 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | UGGT2 | 55757 | UDP-glucose glycoprotein glucosyltransferase 2 | Q9NYU1 |
| C1306459 | Primary malignant neoplasm | UGGT2 | 55757 | UDP-glucose glycoprotein glucosyltransferase 2 | Q9NYU1 |
| C0027051 | Myocardial Infarction | UGGT2 | 55757 | UDP-glucose glycoprotein glucosyltransferase 2 | Q9NYU1 |
| C0235946 | Cerebral atrophy | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C0026650 | Movement Disorders | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C3808991 | NGLY1 deficiency | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C0008489 | Chorea | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C0235991 | Small for gestational age (disorder) | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C0036572 | Seizures | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C0037769 | West Syndrome | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
