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 |
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DisGeNET | July 29, 2024 |
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