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 551 - 575 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0003493 Aortic Diseases VCAM1 7412 vascular cell adhesion molecule 1 P19320
C0243010 Viral Encephalitis VCAM1 7412 vascular cell adhesion molecule 1 P19320
C0023348 Leprosy, Lepromatous VCAM1 7412 vascular cell adhesion molecule 1 P19320
C0035435 Rheumatism VCAM1 7412 vascular cell adhesion molecule 1 P19320
C1335302 Pancreatic Ductal Adenocarcinoma VCAM1 7412 vascular cell adhesion molecule 1 P19320
C0018213 Graves Disease VCAM1 7412 vascular cell adhesion molecule 1 P19320
C0017658 Glomerulonephritis VCAM1 7412 vascular cell adhesion molecule 1 P19320
C0699790 Colon Carcinoma VCAM1 7412 vascular cell adhesion molecule 1 P19320
C0011615 Dermatitis, Atopic VNN2 8875 vanin 2 O95498
C0086196 Eczema, Infantile VNN2 8875 vanin 2 O95498
C0029463 Osteosarcoma VNN2 8875 vanin 2 O95498
C0030246 Pustulosis of Palms and Soles VNN2 8875 vanin 2 O95498
C0025517 Metabolic Diseases VNN2 8875 vanin 2 O95498
C0024530 Malaria VNN2 8875 vanin 2 O95498
C0585442 Osteosarcoma of bone VNN2 8875 vanin 2 O95498
C0033860 Psoriasis VNN2 8875 vanin 2 O95498
C1621958 Glioblastoma Multiforme VNN2 8875 vanin 2 O95498
C1306459 Primary malignant neoplasm VNN2 8875 vanin 2 O95498
C0006826 Malignant Neoplasms VNN2 8875 vanin 2 O95498
C0017636 Glioblastoma VNN2 8875 vanin 2 O95498
C0015624 Fanconi Syndrome VNN2 8875 vanin 2 O95498
C2931187 Nephropathic cystinosis VNN2 8875 vanin 2 O95498
C0033860 Psoriasis VNN1 8876 vanin 1 O95497
C0025517 Metabolic Diseases VNN1 8876 vanin 1 O95497
C0015624 Fanconi Syndrome VNN1 8876 vanin 1 O95497

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Last updated: August 19, 2024