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 |
---|---|---|---|---|---|
C0020615 | Hypoglycemia | DBT | 1629 | dihydrolipoamide branched chain transacylase E2 | P11182 |
C0026850 | Muscular Dystrophy | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0265221 | Walker-Warburg congenital muscular dystrophy | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0007570 | Celiac Disease | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C4721453 | Peripheral Nervous System Diseases | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C1306459 | Primary malignant neoplasm | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0686353 | Muscular Dystrophies, Limb-Girdle | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0036857 | Severe intellectual disability | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0282577 | Congenital Disorders of Glycosylation | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0024198 | Lyme Disease | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0025362 | Mental Retardation | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0699743 | Congenital muscular dystrophy (disorder) | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0009375 | Colonic Neoplasms | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0349566 | Squamous cell carcinoma of tongue | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C1269683 | Major Depressive Disorder | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0007102 | Malignant tumor of colon | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0410174 | Fukuyama Type Congenital Muscular Dystrophy | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C3151184 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9 | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0017638 | Glioma | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0015393 | Eye Abnormalities | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0010038 | Corneal Opacity | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0017601 | Glaucoma | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0026848 | Myopathy | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C4225291 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9 | DAG1 | 1605 | dystroglycan 1 | Q14118 |
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Last updated: August 19, 2024