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 44401 - 44425 of 62743 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Gene Name UniProt ID
C0026848 Myopathy CYP3A5 1577 cytochrome P450 family 3 subfamily A member 5 P20815
C0026848 Myopathy DCN 1634 decorin P07585
C0026848 Myopathy ACE 1636 angiotensin I converting enzyme P12821
C0026848 Myopathy HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0026848 Myopathy ANXA5 308 annexin A5 P08758
C0026848 Myopathy NCAM1 4684 neural cell adhesion molecule 1 P13591
C0026848 Myopathy PIK3C2A 5286 phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha O00443
C0026848 Myopathy INPP5K 51763 inositol polyphosphate-5-phosphatase K Q9BT40
C0026848 Myopathy AGK 55750 acylglycerol kinase Q53H12
C0026848 Myopathy PRNP 5621 prion protein P04156
C0026848 Myopathy PNPLA2 57104 patatin like phospholipase domain containing 2 Q96AD5
C0026848 Myopathy MTMR14 64419 myotubularin related protein 14 Q8NCE2
C0026848 Myopathy SI 6476 sucrase-isomaltase P14410
C0026848 Myopathy SFTPA1 653509 surfactant protein A1 Q8IWL2
C0026848 Myopathy TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0026848 Myopathy COLEC12 81035 collectin subfamily member 12 Q5KU26
C0026848 Myopathy CAT 847 catalase P04040
C0026848 Myopathy DGAT1 8694 diacylglycerol O-acyltransferase 1 O75907
C0026848 Myopathy MGAM 8972 maltase-glucoamylase O43451
C0026848 Myopathy LPIN2 9663 lipin 2 Q92539
C0026848 Myopathy DAG1 1605 dystroglycan 1 Q14118
C0026848 Myopathy G6PC 2538 glucose-6-phosphatase catalytic subunit P35575
C0026848 Myopathy PGAM2 5224 phosphoglycerate mutase 2 P15259
C0026848 Myopathy TPI1 7167 triosephosphate isomerase 1 P60174
C0026848 Myopathy CNTN1 1272 contactin 1 Q12860

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Last updated: August 19, 2024