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 12001 - 12025 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0022336 Creutzfeldt-Jakob disease CHGA 1113 chromogranin A P10645
C0678222 Breast Carcinoma CHGA 1113 chromogranin A P10645
C0014859 Esophageal Neoplasms CHGA 1113 chromogranin A P10645
C2882221 Acute pulmonary embolism CHGA 1113 chromogranin A P10645
C1956346 Coronary Artery Disease CHGA 1113 chromogranin A P10645
C0026769 Multiple Sclerosis CHGA 1113 chromogranin A P10645
C0018801 Heart failure CHGA 1113 chromogranin A P10645
C0009324 Ulcerative Colitis CHGA 1113 chromogranin A P10645
C0030421 Paraganglioma CHGA 1113 chromogranin A P10645
C0206663 Neuroectodermal Tumor, Primitive CHGA 1113 chromogranin A P10645
C0005695 Bladder Neoplasm CHGA 1113 chromogranin A P10645
C0149925 Small cell carcinoma of lung CHGA 1113 chromogranin A P10645
C0022661 Kidney Failure, Chronic CHGA 1113 chromogranin A P10645
C0027051 Myocardial Infarction CHGA 1113 chromogranin A P10645
C0238067 Colitis, Collagenous CHGA 1113 chromogranin A P10645
C0002736 Amyotrophic Lateral Sclerosis CHGA 1113 chromogranin A P10645
C0021390 Inflammatory Bowel Diseases CHGA 1113 chromogranin A P10645
C0700095 Central neuroblastoma CHGA 1113 chromogranin A P10645
C0033578 Prostatic Neoplasms CHGA 1113 chromogranin A P10645
C1857276 Trichohepatoenteric Syndrome CHGA 1113 chromogranin A P10645
C0400822 Colitis, Lymphocytic CHGA 1113 chromogranin A P10645
C0006142 Malignant neoplasm of breast CHGA 1113 chromogranin A P10645
C0007102 Malignant tumor of colon CHGA 1113 chromogranin A P10645
C0027719 Nephrosclerosis CHGA 1113 chromogranin A P10645
C0206695 Carcinoma, Neuroendocrine CHGA 1113 chromogranin A P10645

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Last updated: August 19, 2024