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 14301 - 14325 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0014547 Epilepsies, Partial DAG1 1605 dystroglycan 1 Q14118
C0014547 Epilepsies, Partial PTEN 5728 phosphatase and tensin homolog P60484
C0014548 Epilepsy, Generalized ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0014548 Epilepsy, Generalized GMPPB 29925 GDP-mannose pyrophosphorylase B Q9Y5P6
C0014548 Epilepsy, Generalized MCAT 27349 malonyl-CoA-acyl carrier protein transacylase Q8IVS2
C0014548 Epilepsy, Generalized ME2 4200 malic enzyme 2 P23368
C0014548 Epilepsy, Generalized SLC2A3 6515 solute carrier family 2 member 3 P11169
C0014548 Epilepsy, Generalized CACNA2D2 9254 calcium voltage-gated channel auxiliary subunit alpha2delta 2 Q9NY47
C0014548 Epilepsy, Generalized GAD2 2572 glutamate decarboxylase 2 Q05329
C0014548 Epilepsy, Generalized GLDC 2731 glycine decarboxylase P23378
C0014548 Epilepsy, Generalized ALDH5A1 7915 aldehyde dehydrogenase 5 family member A1 P51649
C0014550 Myoclonic Epilepsy PIGW 284098 phosphatidylinositol glycan anchor biosynthesis class W Q7Z7B1
C0014550 Myoclonic Epilepsy HEXB 3074 hexosaminidase subunit beta P07686
C0014550 Myoclonic Epilepsy ARSA 410 arylsulfatase A P15289
C0014550 Myoclonic Epilepsy ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0014550 Myoclonic Epilepsy EPM2A 7957 EPM2A glucan phosphatase, laforin O95278
C0014550 Myoclonic Epilepsy INPP4A 3631 inositol polyphosphate-4-phosphatase type I A Q96PE3
C0014553 Absence Epilepsy PIGO 84720 phosphatidylinositol glycan anchor biosynthesis class O Q8TEQ8
C0014553 Absence Epilepsy CANX 821 calnexin P27824
C0014553 Absence Epilepsy ALPI 248 alkaline phosphatase, intestinal P09923
C0014553 Absence Epilepsy ALPP 250 alkaline phosphatase, placental P05187
C0014553 Absence Epilepsy CACNA2D2 9254 calcium voltage-gated channel auxiliary subunit alpha2delta 2 Q9NY47
C0014553 Absence Epilepsy PDIA3 2923 protein disulfide isomerase family A member 3 P30101
C0014553 Absence Epilepsy PLCB4 5332 phospholipase C beta 4 Q15147
C0014556 Epilepsy, Temporal Lobe MGAT1 4245 alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase P26572

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Last updated: August 19, 2024