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 44601 - 44625 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0003850 Arteriosclerosis DAG1 1605 dystroglycan 1 Q14118
C0546837 Malignant neoplasm of esophagus DAG1 1605 dystroglycan 1 Q14118
C0027121 Myositis DAG1 1605 dystroglycan 1 Q14118
C1449563 Cardiomyopathy, Familial Idiopathic DAG1 1605 dystroglycan 1 Q14118
C0011633 Dermatomyositis DAG1 1605 dystroglycan 1 Q14118
C0235974 Pancreatic carcinoma DAG1 1605 dystroglycan 1 Q14118
C0032897 Prader-Willi Syndrome DAG1 1605 dystroglycan 1 Q14118
C0476089 Endometrial Carcinoma DAG1 1605 dystroglycan 1 Q14118
C0024141 Lupus Erythematosus, Systemic DAG1 1605 dystroglycan 1 Q14118
C0010964 Dandy-Walker Syndrome DAG1 1605 dystroglycan 1 Q14118
C0678222 Breast Carcinoma DAG1 1605 dystroglycan 1 Q14118
C1335302 Pancreatic Ductal Adenocarcinoma DAG1 1605 dystroglycan 1 Q14118
C0009324 Ulcerative Colitis DAG1 1605 dystroglycan 1 Q14118
C0018801 Heart failure DAG1 1605 dystroglycan 1 Q14118
C0266551 Congenital coloboma of iris DAG1 1605 dystroglycan 1 Q14118
C1458155 Mammary Neoplasms DAG1 1605 dystroglycan 1 Q14118
C0023467 Leukemia, Myelocytic, Acute DAG1 1605 dystroglycan 1 Q14118
C0024266 Lymphocytic Choriomeningitis DAG1 1605 dystroglycan 1 Q14118
C0524620 Metabolic Syndrome X DAG1 1605 dystroglycan 1 Q14118
C0917713 Becker Muscular Dystrophy DAG1 1605 dystroglycan 1 Q14118
C0332915 Congenital failure of fusion DAG1 1605 dystroglycan 1 Q14118
C0010417 Cryptorchidism DAG1 1605 dystroglycan 1 Q14118
C0006142 Malignant neoplasm of breast DAG1 1605 dystroglycan 1 Q14118
C0282687 Hemorrhagic Fever, Ebola DAG1 1605 dystroglycan 1 Q14118
C0023418 leukemia DAG1 1605 dystroglycan 1 Q14118

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Last updated: August 19, 2024