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 39351 - 39375 of 62743 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0024530 Malaria PGD 5226 phosphogluconate dehydrogenase P52209
C0024530 Malaria FUT9 10690 fucosyltransferase 9 Q9Y231
C0024530 Malaria SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0024530 Malaria CHI3L1 1116 chitinase 3 like 1 P36222
C0024523 Malabsorption Syndrome SLC2A5 6518 solute carrier family 2 member 5 P22732
C0024523 Malabsorption Syndrome CD55 1604 CD55 molecule (Cromer blood group) P08174
C0024523 Malabsorption Syndrome SLC2A2 6514 solute carrier family 2 member 2 P11168
C0024523 Malabsorption Syndrome HSD3B7 80270 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 Q9H2F3
C0024523 Malabsorption Syndrome LPIN2 9663 lipin 2 Q92539
C0024523 Malabsorption Syndrome PNLIP 5406 pancreatic lipase P16233
C0024523 Malabsorption Syndrome MMUT 4594 methylmalonyl-CoA mutase P22033
C0024523 Malabsorption Syndrome TYMP 1890 thymidine phosphorylase P19971
C0024523 Malabsorption Syndrome SI 6476 sucrase-isomaltase P14410
C0024523 Malabsorption Syndrome ENPP1 5167 ectonucleotide pyrophosphatase/phosphodiesterase 1 P22413
C0024523 Malabsorption Syndrome OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0024523 Malabsorption Syndrome AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0024523 Malabsorption Syndrome SLC5A1 6523 solute carrier family 5 member 1 P13866
C0024523 Malabsorption Syndrome MGLL 11343 monoglyceride lipase Q99685
C0024523 Malabsorption Syndrome DGAT1 8694 diacylglycerol O-acyltransferase 1 O75907
C0024523 Malabsorption Syndrome LCT 3938 lactase P09848
C0024523 Malabsorption Syndrome ACE 1636 angiotensin I converting enzyme P12821
C0024523 Malabsorption Syndrome PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C0024523 Malabsorption Syndrome MPI 4351 mannose phosphate isomerase P34949
C0024523 Malabsorption Syndrome CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0024523 Malabsorption Syndrome AGA 175 aspartylglucosaminidase P20933

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Last updated: August 19, 2024