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 59751 - 59775 of 62743 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Gene Name UniProt ID
C0014518 Toxic Epidermal Necrolysis CYP3A4 1576 cytochrome P450 family 3 subfamily A member 4 P08684
C0014518 Toxic Epidermal Necrolysis ALOX5 240 arachidonate 5-lipoxygenase P09917
C0014518 Toxic Epidermal Necrolysis PTGIS 5740 prostaglandin I2 synthase Q16647
C0600327 Toxic Shock Syndrome FUT2 2524 fucosyltransferase 2 Q10981
C0600327 Toxic Shock Syndrome ENO2 2026 enolase 2 P09104
C0600327 Toxic Shock Syndrome SELL 6402 selectin L P14151
C0600327 Toxic Shock Syndrome HSPG2 3339 heparan sulfate proteoglycan 2 P98160
C0040558 Toxoplasmosis FUT3 2525 fucosyltransferase 3 (Lewis blood group) P21217
C0040558 Toxoplasmosis FUT2 2524 fucosyltransferase 2 Q10981
C0040558 Toxoplasmosis FDPS 2224 farnesyl diphosphate synthase P14324
C0040558 Toxoplasmosis ALOX12 239 arachidonate 12-lipoxygenase, 12S type P18054
C0040558 Toxoplasmosis ICAM1 3383 intercellular adhesion molecule 1 P05362
C0040558 Toxoplasmosis ACO1 48 aconitase 1 P21399
C0040558 Toxoplasmosis GPAT3 84803 glycerol-3-phosphate acyltransferase 3 Q53EU6
C0040558 Toxoplasmosis DGAT1 8694 diacylglycerol O-acyltransferase 1 O75907
C0040558 Toxoplasmosis CD44 960 CD44 molecule (Indian blood group) P16070
C0040558 Toxoplasmosis HSPG2 3339 heparan sulfate proteoglycan 2 P98160
C0040558 Toxoplasmosis IL18R1 8809 interleukin 18 receptor 1 Q13478
C0040558 Toxoplasmosis TPI1 7167 triosephosphate isomerase 1 P60174
C0040558 Toxoplasmosis MICA 100507436 MHC class I polypeptide-related sequence A Q29983
C0040560 Toxoplasmosis, Congenital ALOX12 239 arachidonate 12-lipoxygenase, 12S type P18054
C0040580 Tracheal Diseases MPI 4351 mannose phosphate isomerase P34949
C0040580 Tracheal Diseases DPEP1 1800 dipeptidase 1 P16444
C0040580 Tracheal Diseases ALDH2 217 aldehyde dehydrogenase 2 family member P05091
C0040580 Tracheal Diseases MRC1 4360 mannose receptor C-type 1 P22897

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Last updated: August 19, 2024