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 176 - 200 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0001175 Acquired Immunodeficiency Syndrome GPAT3 84803 glycerol-3-phosphate acyltransferase 3 Q53EU6
C0001175 Acquired Immunodeficiency Syndrome DGKI 9162 diacylglycerol kinase iota O75912
C0001175 Acquired Immunodeficiency Syndrome CD14 929 CD14 molecule P08571
C0001175 Acquired Immunodeficiency Syndrome UNG 7374 uracil DNA glycosylase P13051
C0001175 Acquired Immunodeficiency Syndrome MICA 100507436 MHC class I polypeptide-related sequence A Q29983
C0001175 Acquired Immunodeficiency Syndrome CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0001175 Acquired Immunodeficiency Syndrome PLAUR 5329 plasminogen activator, urokinase receptor Q03405
C0001175 Acquired Immunodeficiency Syndrome PRNP 5621 prion protein F7VJQ1
C0001175 Acquired Immunodeficiency Syndrome BST2 684 bone marrow stromal cell antigen 2 Q10589
C0001206 Acromegaly CALR 811 calreticulin P27797
C0001206 Acromegaly KL 9365 klotho Q9UEF7
C0001206 Acromegaly ACE 1636 angiotensin I converting enzyme P12821
C0001206 Acromegaly ALPP 250 alkaline phosphatase, placental P05187
C0001206 Acromegaly ATRNL1 26033 attractin like 1 Q5VV63
C0001206 Acromegaly HSD11B1 3290 hydroxysteroid 11-beta dehydrogenase 1 P28845
C0001206 Acromegaly LGALS3 3958 galectin 3 P17931
C0001206 Acromegaly LPL 4023 lipoprotein lipase P06858
C0001206 Acromegaly NAMPT 10135 nicotinamide phosphoribosyltransferase P43490
C0001206 Acromegaly RENBP 5973 renin binding protein P51606
C0001206 Acromegaly CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C0001206 Acromegaly DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0001231 ACTH Syndrome, Ectopic SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0001231 ACTH Syndrome, Ectopic HSD11B2 3291 hydroxysteroid 11-beta dehydrogenase 2 P80365
C0001261 Actinomycosis CAT 847 catalase P04040
C0001306 Acute alcoholic liver disease CEACAM5 1048 CEA cell adhesion molecule 5 P06731

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Last updated: August 19, 2024