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 14176 - 14200 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0041207 Truncus Arteriosus, Persistent COMT 1312 catechol-O-methyltransferase P21964
C0021141 Inappropriate ADH Syndrome COMT 1312 catechol-O-methyltransferase P21964
C1333001 Childhood Renal Cell Carcinoma COMT 1312 catechol-O-methyltransferase P21964
C0269102 Endometrioma CPM 1368 carboxypeptidase M P14384
C0009402 Colorectal Carcinoma CPM 1368 carboxypeptidase M P14384
C0003467 Anxiety CPM 1368 carboxypeptidase M P14384
C0006826 Malignant Neoplasms CPM 1368 carboxypeptidase M P14384
C0023827 liposarcoma CPM 1368 carboxypeptidase M P14384
C0278608 Adult Liposarcoma CPM 1368 carboxypeptidase M P14384
C1306459 Primary malignant neoplasm CPM 1368 carboxypeptidase M P14384
C0152013 Adenocarcinoma of lung (disorder) CPM 1368 carboxypeptidase M P14384
C1266129 Atypical Lipoma CPM 1368 carboxypeptidase M P14384
C0037116 Silicosis CPM 1368 carboxypeptidase M P14384
C3489413 Lipomatosis, Multiple CPM 1368 carboxypeptidase M P14384
C0205825 Liposarcoma, Pleomorphic CPM 1368 carboxypeptidase M P14384
C1370889 Liposarcoma, well differentiated CPM 1368 carboxypeptidase M P14384
C0027651 Neoplasms CPM 1368 carboxypeptidase M P14384
C0006142 Malignant neoplasm of breast CPM 1368 carboxypeptidase M P14384
C0154830 Proliferative diabetic retinopathy CPM 1368 carboxypeptidase M P14384
C0004238 Atrial Fibrillation CPM 1368 carboxypeptidase M P14384
C0003537 Aphasia CPM 1368 carboxypeptidase M P14384
C0023798 Lipoma CPM 1368 carboxypeptidase M P14384
C0678222 Breast Carcinoma CPM 1368 carboxypeptidase M P14384
C1565489 Renal Insufficiency CPM 1368 carboxypeptidase M P14384
C0279984 Childhood Liposarcoma CPM 1368 carboxypeptidase M P14384

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Last updated: August 19, 2024