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 14426 - 14450 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0037274 Dermatologic disorders CD14 929 CD14 molecule P08571
C0085437 Meningitis, Bacterial CD14 929 CD14 molecule P08571
C0162429 Malnutrition CD14 929 CD14 molecule P08571
C0010072 Coronary Thrombosis CD14 929 CD14 molecule P08571
C0017205 Gaucher Disease CD14 929 CD14 molecule P08571
C0013377 Dysgerminoma CD14 929 CD14 molecule P08571
C0004106 Astigmatism MELTF 4241 melanotransferrin P08582
C0009402 Colorectal Carcinoma MELTF 4241 melanotransferrin P08582
C0025202 melanoma MELTF 4241 melanotransferrin P08582
C0027651 Neoplasms MELTF 4241 melanotransferrin P08582
C1332986 Childhood Osteosarcoma MELTF 4241 melanotransferrin P08582
C1306459 Primary malignant neoplasm MELTF 4241 melanotransferrin P08582
C0007097 Carcinoma MELTF 4241 melanotransferrin P08582
C0024623 Malignant neoplasm of stomach MELTF 4241 melanotransferrin P08582
C0006826 Malignant Neoplasms MELTF 4241 melanotransferrin P08582
C0002395 Alzheimer's Disease MELTF 4241 melanotransferrin P08582
C0007847 Malignant tumor of cervix MELTF 4241 melanotransferrin P08582
C0020459 Hyperinsulinism MELTF 4241 melanotransferrin P08582
C0585442 Osteosarcoma of bone MELTF 4241 melanotransferrin P08582
C0085110 Severe Combined Immunodeficiency MELTF 4241 melanotransferrin P08582
C0206663 Neuroectodermal Tumor, Primitive MELTF 4241 melanotransferrin P08582
C0017638 Glioma MELTF 4241 melanotransferrin P08582
C0206633 Angiomyolipoma MELTF 4241 melanotransferrin P08582
C0152013 Adenocarcinoma of lung (disorder) MELTF 4241 melanotransferrin P08582
C0151779 Cutaneous Melanoma MELTF 4241 melanotransferrin P08582

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Last updated: August 19, 2024