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 40576 - 40600 of 62743 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0023895 Liver diseases CD1D 912 CD1d molecule P15813
C0023895 Liver diseases CD14 929 CD14 molecule P08571
C0023895 Liver diseases CYP7B1 9420 cytochrome P450 family 7 subfamily B member 1 O75881
C0023895 Liver diseases NAMPT 10135 nicotinamide phosphoribosyltransferase P43490
C0023895 Liver diseases SLC35A2 7355 solute carrier family 35 member A2 P78381
C0023895 Liver diseases AKR1C1 1645 aldo-keto reductase family 1 member C1 Q04828
C0023895 Liver diseases GALT 2592 galactose-1-phosphate uridylyltransferase P07902
C0023895 Liver diseases G6PC 2538 glucose-6-phosphatase catalytic subunit P35575
C0023895 Liver diseases GLO1 2739 glyoxalase I Q04760
C0023895 Liver diseases GPC3 2719 glypican 3 P51654
C0023895 Liver diseases HK3 3101 hexokinase 3 P52790
C0023895 Liver diseases MTAP 4507 methylthioadenosine phosphorylase Q13126
C0023895 Liver diseases PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C0023895 Liver diseases TALDO1 6888 transaldolase 1 P37837
C0023895 Liver diseases RENBP 5973 renin binding protein P51606
C0023895 Liver diseases AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0023895 Liver diseases MICA 100507436 MHC class I polypeptide-related sequence A Q29983
C0023895 Liver diseases RGN 9104 regucalcin Q15493
C0023895 Liver diseases PEMT 10400 phosphatidylethanolamine N-methyltransferase Q9UBM1
C0023895 Liver diseases CEACAM7 1087 CEA cell adhesion molecule 7 Q14002
C0023895 Liver diseases ADH1A 124 alcohol dehydrogenase 1A (class I), alpha polypeptide P07327
C0023895 Liver diseases TMEM199 147007 transmembrane protein 199 Q8N511
C0023895 Liver diseases CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0023895 Liver diseases CYP1B1 1545 cytochrome P450 family 1 subfamily B member 1 Q16678
C0023895 Liver diseases CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261

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Last updated: August 19, 2024