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 251 - 275 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0001342 Acute periodontitis CYP1A1 1543 cytochrome P450 family 1 subfamily A member 1 P04798
C0001342 Acute periodontitis FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C0001342 Acute periodontitis MBL2 4153 mannose binding lectin 2 P11226
C0001342 Acute periodontitis SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0001342 Acute periodontitis MMP25 64386 matrix metallopeptidase 25 Q9NPA2
C0001342 Acute periodontitis SIGLEC5 8778 sialic acid binding Ig like lectin 5 O15389
C0001342 Acute periodontitis CD14 929 CD14 molecule P08571
C0001342 Acute periodontitis PTGS2 5743 prostaglandin-endoperoxide synthase 2 P35354
C0001344 Acute pharyngitis GALNS 2588 galactosamine (N-acetyl)-6-sulfatase P34059
C0001344 Acute pharyngitis PTGS2 5743 prostaglandin-endoperoxide synthase 2 P35354
C0001361 Acute tonsillitis NT5E 4907 5'-nucleotidase ecto P21589
C0001363 Acute vascular insufficiency of intestine (disorder) PCYT1A 5130 phosphate cytidylyltransferase 1, choline, alpha P49585
C0001403 Addison Disease UGT2B28 54490 UDP glucuronosyltransferase family 2 member B28 Q9BY64
C0001403 Addison Disease CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0001403 Addison Disease GLUL 2752 glutamate-ammonia ligase P15104
C0001403 Addison Disease HSD11B1 3290 hydroxysteroid 11-beta dehydrogenase 1 P28845
C0001403 Addison Disease TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0001403 Addison Disease SGPL1 8879 sphingosine-1-phosphate lyase 1 O95470
C0001403 Addison Disease CD14 929 CD14 molecule P08571
C0001403 Addison Disease MICA 100507436 MHC class I polypeptide-related sequence A Q29983
C0001403 Addison Disease CYP11A1 1583 cytochrome P450 family 11 subfamily A member 1 P05108
C0001403 Addison Disease CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0001403 Addison Disease CLEC16A 23274 C-type lectin domain containing 16A Q2KHT3
C0001403 Addison Disease GAD2 2572 glutamate decarboxylase 2 Q05329
C0001403 Addison Disease HSD17B4 3295 hydroxysteroid 17-beta dehydrogenase 4 P51659

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Last updated: August 19, 2024