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 601 - 625 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C2711227 Steatohepatitis VNN1 8876 vanin 1 O95497
C0011615 Dermatitis, Atopic VNN1 8876 vanin 1 O95497
C0010346 Crohn Disease UST 10090 uronyl 2-sulfotransferase Q9Y2C2
C0038013 Ankylosing spondylitis UST 10090 uronyl 2-sulfotransferase Q9Y2C2
C0006826 Malignant Neoplasms UST 10090 uronyl 2-sulfotransferase Q9Y2C2
C0004238 Atrial Fibrillation UST 10090 uronyl 2-sulfotransferase Q9Y2C2
C0235480 Paroxysmal atrial fibrillation UST 10090 uronyl 2-sulfotransferase Q9Y2C2
C0269102 Endometrioma UST 10090 uronyl 2-sulfotransferase Q9Y2C2
C0029408 Degenerative polyarthritis UST 10090 uronyl 2-sulfotransferase Q9Y2C2
C0014175 Endometriosis UST 10090 uronyl 2-sulfotransferase Q9Y2C2
C0740394 Hyperuricemia UMOD 7369 uromodulin P07911
C0020538 Hypertensive disease UMOD 7369 uromodulin P07911
C0262655 Recurrent urinary tract infection UMOD 7369 uromodulin P07911
C0022661 Kidney Failure, Chronic UMOD 7369 uromodulin P07911
C0011860 Diabetes Mellitus, Non-Insulin-Dependent UMOD 7369 uromodulin P07911
C0687120 Nephronophthisis UMOD 7369 uromodulin P07911
C1561643 Chronic Kidney Diseases UMOD 7369 uromodulin P07911
C0004153 Atherosclerosis UMOD 7369 uromodulin P07911
C0085580 Essential Hypertension UMOD 7369 uromodulin P07911
C0027707 Nephritis, Interstitial UMOD 7369 uromodulin P07911
C4551496 Hyperuricemic Nephropathy, Familial Juvenile 1 UMOD 7369 uromodulin P07911
C2751310 Hyperuricemic Nephropathy, Familial Juvenile 2 UMOD 7369 uromodulin P07911
C2939174 Medullary cystic disease UMOD 7369 uromodulin P07911
C0241397 Triphalangeal thumb UMOD 7369 uromodulin P07911
C0018802 Congestive heart failure UMOD 7369 uromodulin P07911

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Last updated: August 19, 2024