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 12951 - 12975 of 62743 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Gene Name UniProt ID
C0235480 Paroxysmal atrial fibrillation COG5 10466 component of oligomeric golgi complex 5 Q9UP83
C0235480 Paroxysmal atrial fibrillation ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0235480 Paroxysmal atrial fibrillation ADH1B 125 alcohol dehydrogenase 1B (class I), beta polypeptide P00325
C0235480 Paroxysmal atrial fibrillation ACE 1636 angiotensin I converting enzyme P12821
C0235480 Paroxysmal atrial fibrillation DLD 1738 dihydrolipoamide dehydrogenase P09622
C0235480 Paroxysmal atrial fibrillation RGMB 285704 repulsive guidance molecule BMP co-receptor b Q6NW40
C0235480 Paroxysmal atrial fibrillation SELE 6401 selectin E P16581
C0235480 Paroxysmal atrial fibrillation VCAM1 7412 vascular cell adhesion molecule 1 P19320
C0235480 Paroxysmal atrial fibrillation HSPG2 3339 heparan sulfate proteoglycan 2 P98160
C0235480 Paroxysmal atrial fibrillation CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0235480 Paroxysmal atrial fibrillation DGKB 1607 diacylglycerol kinase beta Q9Y6T7
C0235480 Paroxysmal atrial fibrillation SLC35F1 222553 solute carrier family 35 member F1 Q5T1Q4
C0235480 Paroxysmal atrial fibrillation SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C4551506 Paroxysmal Nonkinesigenic Dyskinesia 1 CD14 929 CD14 molecule P08571
C4551506 Paroxysmal Nonkinesigenic Dyskinesia 1 UGP2 7360 UDP-glucose pyrophosphorylase 2 Q16851
C4551506 Paroxysmal Nonkinesigenic Dyskinesia 1 CEACAM7 1087 CEA cell adhesion molecule 7 Q14002
C0242422 Parkinsonian Disorders ST8SIA1 6489 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 Q92185
C0242422 Parkinsonian Disorders GBA 2629 glucosylceramidase beta P04062
C0242422 Parkinsonian Disorders GLB1 2720 galactosidase beta 1 P16278
C0242422 Parkinsonian Disorders OGA 10724 O-GlcNAcase O60502
C0242422 Parkinsonian Disorders ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0242422 Parkinsonian Disorders COMT 1312 catechol-O-methyltransferase P21964
C0242422 Parkinsonian Disorders PARP1 142 poly(ADP-ribose) polymerase 1 P09874
C0242422 Parkinsonian Disorders ENO2 2026 enolase 2 P09104
C0242422 Parkinsonian Disorders SIRT2 22933 sirtuin 2 Q8IXJ6

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Last updated: August 19, 2024