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 60751 - 60775 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0009806 Constipation SDC1 6382 syndecan 1 P18827
C0033687 Proteinuria SDC1 6382 syndecan 1 P18827
C0025202 melanoma SDC2 6383 syndecan 2 P34741
C0027651 Neoplasms SDC2 6383 syndecan 2 P34741
C0029463 Osteosarcoma SDC2 6383 syndecan 2 P34741
C0040136 Thyroid Neoplasm SDC2 6383 syndecan 2 P34741
C0585442 Osteosarcoma of bone SDC2 6383 syndecan 2 P34741
C1510489 Cerebral Amyloid Angiopathy, Hereditary SDC2 6383 syndecan 2 P34741
C0022658 Kidney Diseases SDC2 6383 syndecan 2 P34741
C0016057 Fibrosarcoma SDC2 6383 syndecan 2 P34741
C1306759 Eosinophilic disorder SDC2 6383 syndecan 2 P34741
C0006142 Malignant neoplasm of breast SDC2 6383 syndecan 2 P34741
C0007102 Malignant tumor of colon SDC2 6383 syndecan 2 P34741
C0006826 Malignant Neoplasms SDC2 6383 syndecan 2 P34741
C0278595 Adult Fibrosarcoma SDC2 6383 syndecan 2 P34741
C2239176 Liver carcinoma SDC2 6383 syndecan 2 P34741
C1800706 Idiopathic Pulmonary Fibrosis SDC2 6383 syndecan 2 P34741
C1332986 Childhood Osteosarcoma SDC2 6383 syndecan 2 P34741
C0001430 Adenoma SDC2 6383 syndecan 2 P34741
C0699790 Colon Carcinoma SDC2 6383 syndecan 2 P34741
C0009402 Colorectal Carcinoma SDC2 6383 syndecan 2 P34741
C0003873 Rheumatoid Arthritis SDC2 6383 syndecan 2 P34741
C0020473 Hyperlipidemia SDC2 6383 syndecan 2 P34741
C0016667 Fragile X Syndrome SDC2 6383 syndecan 2 P34741
C0018802 Congestive heart failure SDC2 6383 syndecan 2 P34741

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Last updated: August 19, 2024