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
Displaying entries 44526 - 44550 of 62743 in total
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