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 53676 - 53700 of 62743 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Gene Name UniProt ID
C0007097 Carcinoma PLA2G1B 5319 phospholipase A2 group IB P04054
C0007097 Carcinoma PLAUR 5329 plasminogen activator, urokinase receptor Q03405
C0007097 Carcinoma PLD1 5337 phospholipase D1 Q13393
C0007097 Carcinoma PRKAA2 5563 protein kinase AMP-activated catalytic subunit alpha 2 P54646
C0007097 Carcinoma LY6K 54742 lymphocyte antigen 6 family member K Q17RY6
C0007097 Carcinoma PRNP 5621 prion protein F7VJQ1
C0007097 Carcinoma PRPS1 5631 phosphoribosyl pyrophosphate synthetase 1 P60891
C0007097 Carcinoma PTEN 5728 phosphatase and tensin homolog P60484
C0007097 Carcinoma BAAT 570 bile acid-CoA:amino acid N-acyltransferase Q14032
C0007097 Carcinoma PTGS2 5743 prostaglandin-endoperoxide synthase 2 P35354
C0007097 Carcinoma PTGDS 5730 prostaglandin D2 synthase P41222
C0007097 Carcinoma SFTPC 6440 surfactant protein C P11686
C0007097 Carcinoma GOLPH3 64083 golgi phosphoprotein 3 Q9H4A6
C0007097 Carcinoma TKT 7086 transketolase P29401
C0007097 Carcinoma TKTL1 8277 transketolase like 1 P51854
C3553571 Carbohydrate deficient glycoprotein syndrome type 2k TMEM165 55858 transmembrane protein 165 Q9HC07
C0751753 Carbamoyl-Phosphate Synthase I Deficiency Disease UMPS 7372 uridine monophosphate synthetase P11172
C0751753 Carbamoyl-Phosphate Synthase I Deficiency Disease GLUL 2752 glutamate-ammonia ligase P15104
C0751753 Carbamoyl-Phosphate Synthase I Deficiency Disease CAT 847 catalase P04040
C0751753 Carbamoyl-Phosphate Synthase I Deficiency Disease PTEN 5728 phosphatase and tensin homolog P60484
C0340803 Capillary malformation (disorder) ICAM1 3383 intercellular adhesion molecule 1 P05362
C0340803 Capillary malformation (disorder) MAG 4099 myelin associated glycoprotein P20916
C0340803 Capillary malformation (disorder) PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C0340803 Capillary malformation (disorder) KLRB1 3820 killer cell lectin like receptor B1 Q12918
C0343084 Capillary Leak Syndrome ICAM1 3383 intercellular adhesion molecule 1 P05362

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Last updated: August 19, 2024