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 16101 - 16125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
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
C1861922 CAMPOMELIC DYSPLASIA DAG1 1605 dystroglycan 1 Q14118
C3714756 Intellectual Disability DAG1 1605 dystroglycan 1 Q14118
C0241005 Creatine phosphokinase serum increased DAG1 1605 dystroglycan 1 Q14118
C3495559 Juvenile arthritis DAG1 1605 dystroglycan 1 Q14118
C0008312 Primary biliary cirrhosis DAG1 1605 dystroglycan 1 Q14118
C0004153 Atherosclerosis DAG1 1605 dystroglycan 1 Q14118
C1852502 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT DAG1 1605 dystroglycan 1 Q14118
C0023092 Lassa Fever DAG1 1605 dystroglycan 1 Q14118
C0520947 Clumsiness - motor delay DAG1 1605 dystroglycan 1 Q14118
C0010346 Crohn Disease DAG1 1605 dystroglycan 1 Q14118
C0038013 Ankylosing spondylitis DAG1 1605 dystroglycan 1 Q14118
C0001418 Adenocarcinoma DAG1 1605 dystroglycan 1 Q14118
C0000768 Congenital Abnormality DAG1 1605 dystroglycan 1 Q14118
C1332977 Childhood Leukemia DAG1 1605 dystroglycan 1 Q14118
C0027651 Neoplasms DAG1 1605 dystroglycan 1 Q14118
C0086543 Cataract DAG1 1605 dystroglycan 1 Q14118
C0018802 Congestive heart failure DAG1 1605 dystroglycan 1 Q14118
C1853926 NONAKA MYOPATHY DAG1 1605 dystroglycan 1 Q14118
C0011265 Presenile dementia DAG1 1605 dystroglycan 1 Q14118
C0035305 Retinal Detachment DAG1 1605 dystroglycan 1 Q14118
C0699790 Colon Carcinoma DAG1 1605 dystroglycan 1 Q14118
C0600139 Prostate carcinoma DAG1 1605 dystroglycan 1 Q14118
C1836373 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K DAG1 1605 dystroglycan 1 Q14118

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Last updated: August 19, 2024