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 13201 - 13225 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0013238 Dry Eye Syndromes HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0013238 Dry Eye Syndromes ACAT1 38 acetyl-CoA acetyltransferase 1 P24752
C0013238 Dry Eye Syndromes ICAM1 3383 intercellular adhesion molecule 1 P05362
C0013238 Dry Eye Syndromes LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0013238 Dry Eye Syndromes LGALS3 3958 galectin 3 P17931
C0013238 Dry Eye Syndromes CNTN3 5067 contactin 3 Q9P232
C0013238 Dry Eye Syndromes SFTPD 6441 surfactant protein D P35247
C0013238 Dry Eye Syndromes ELOVL1 64834 ELOVL fatty acid elongase 1 Q9BW60
C0013238 Dry Eye Syndromes ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0013238 Dry Eye Syndromes RGN 9104 regucalcin Q15493
C0013238 Dry Eye Syndromes PTGDS 5730 prostaglandin D2 synthase P41222
C0013238 Dry Eye Syndromes PTGS2 5743 prostaglandin-endoperoxide synthase 2 P35354
C0013238 Dry Eye Syndromes SOAT1 6646 sterol O-acyltransferase 1 P35610
C0013264 Muscular Dystrophy, Duchenne B4GALNT2 124872 beta-1,4-N-acetyl-galactosaminyltransferase 2 Q8NHY0
C0013264 Muscular Dystrophy, Duchenne FKTN 2218 fukutin O75072
C0013264 Muscular Dystrophy, Duchenne XYLT1 64131 xylosyltransferase 1 Q86Y38
C0013264 Muscular Dystrophy, Duchenne ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0013264 Muscular Dystrophy, Duchenne LARGE1 9215 LARGE xylosyl- and glucuronyltransferase 1 O95461
C0013264 Muscular Dystrophy, Duchenne GLB1 2720 galactosidase beta 1 P16278
C0013264 Muscular Dystrophy, Duchenne PARP1 142 poly(ADP-ribose) polymerase 1 P09874
C0013264 Muscular Dystrophy, Duchenne ENO1 2023 enolase 1 P06733
C0013264 Muscular Dystrophy, Duchenne G6PD 2539 glucose-6-phosphate dehydrogenase P11413
C0013264 Muscular Dystrophy, Duchenne HPRT1 3251 hypoxanthine phosphoribosyltransferase 1 P00492
C0013264 Muscular Dystrophy, Duchenne APRT 353 adenine phosphoribosyltransferase P07741
C0013264 Muscular Dystrophy, Duchenne IGF2R 3482 insulin like growth factor 2 receptor P11717

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Last updated: August 19, 2024