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 48476 - 48500 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C2674616 FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder) PLB1 151056 phospholipase B1 Q6P1J6
C1839780 FRAGILE X TREMOR/ATAXIA SYNDROME PLB1 151056 phospholipase B1 Q6P1J6
C0003873 Rheumatoid Arthritis PLB1 151056 phospholipase B1 Q6P1J6
C0684249 Carcinoma of lung PLB1 151056 phospholipase B1 Q6P1J6
C1762616 Meningioma, benign, no ICD-O subtype PLB1 151056 phospholipase B1 Q6P1J6
C0003175 Anthrax disease PLB1 151056 phospholipase B1 Q6P1J6
C0004135 Ataxia Telangiectasia PLB1 151056 phospholipase B1 Q6P1J6
C0027697 Nephritis PLB1 151056 phospholipase B1 Q6P1J6
C1861172 Venous Thromboembolism PLB1 151056 phospholipase B1 Q6P1J6
C0344315 Depressed mood PLB1 151056 phospholipase B1 Q6P1J6
C0009021 Clonorchiasis PLB1 151056 phospholipase B1 Q6P1J6
C0239946 Fibrosis, Liver PLB1 151056 phospholipase B1 Q6P1J6
C0086543 Cataract PLB1 151056 phospholipase B1 Q6P1J6
C0013595 Eczema PLB1 151056 phospholipase B1 Q6P1J6
C0024894 Mastitis PLB1 151056 phospholipase B1 Q6P1J6
C1853578 Neuroferritinopathy PLB1 151056 phospholipase B1 Q6P1J6
C0014038 Encephalitis PLB1 151056 phospholipase B1 Q6P1J6
C0010674 Cystic Fibrosis PLB1 151056 phospholipase B1 Q6P1J6
C0752121 Spinocerebellar Ataxia Type 2 PLB1 151056 phospholipase B1 Q6P1J6
C0476089 Endometrial Carcinoma PLB1 151056 phospholipase B1 Q6P1J6
C0018621 Hay fever PLB1 151056 phospholipase B1 Q6P1J6
C0524851 Neurodegenerative Disorders PLB1 151056 phospholipase B1 Q6P1J6
C0027726 Nephrotic Syndrome PLB1 151056 phospholipase B1 Q6P1J6
C0023418 leukemia PLB1 151056 phospholipase B1 Q6P1J6
C0700095 Central neuroblastoma PLB1 151056 phospholipase B1 Q6P1J6

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Last updated: August 19, 2024