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 14276 - 14300 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0014544 Epilepsy SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0014544 Epilepsy DHCR24 1718 24-dehydrocholesterol reductase Q15392
C0014544 Epilepsy SLC35F1 222553 solute carrier family 35 member F1 Q5T1Q4
C0014544 Epilepsy GAD2 2572 glutamate decarboxylase 2 Q05329
C0014544 Epilepsy ALOX15 246 arachidonate 15-lipoxygenase P16050
C0014544 Epilepsy AMT 275 aminomethyltransferase P48728
C0014544 Epilepsy ACADS 35 acyl-CoA dehydrogenase short chain P16219
C0014544 Epilepsy ARSD 414 arylsulfatase D P51689
C0014544 Epilepsy ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0014544 Epilepsy ALDH7A1 501 aldehyde dehydrogenase 7 family member A1 P49419
C0014544 Epilepsy PAFAH1B1 5048 platelet activating factor acetylhydrolase 1b regulatory subunit 1 P43034
C0014544 Epilepsy PIK3CB 5291 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta P42338
C0014544 Epilepsy PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C0014544 Epilepsy PLA2G1B 5319 phospholipase A2 group IB P04054
C0014544 Epilepsy PRNP 5621 prion protein F7VJQ1
C0014544 Epilepsy PTEN 5728 phosphatase and tensin homolog P60484
C0014544 Epilepsy PTGS2 5743 prostaglandin-endoperoxide synthase 2 P35354
C0014544 Epilepsy SHMT1 6470 serine hydroxymethyltransferase 1 P34896
C0014544 Epilepsy CNTN2 6900 contactin 2 Q02246
C0014544 Epilepsy ALDH5A1 7915 aldehyde dehydrogenase 5 family member A1 P51649
C0014544 Epilepsy CACNA2D1 781 calcium voltage-gated channel auxiliary subunit alpha2delta 1 P54289
C0014544 Epilepsy DGKE 8526 diacylglycerol kinase epsilon P52429
C0014547 Epilepsies, Partial SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0014547 Epilepsies, Partial GAD1 2571 glutamate decarboxylase 1 Q99259
C0014547 Epilepsies, Partial SLC33A1 9197 solute carrier family 33 member 1 O00400

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Last updated: August 19, 2024