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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 |
| Disease ID | Disease Name ▲ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0030567 | Parkinson Disease | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C0030567 | Parkinson Disease | PKD1 | 5310 | polycystin 1, transient receptor potential channel interacting | P98161 |
| C0030567 | Parkinson Disease | PLA2G1B | 5319 | phospholipase A2 group IB | P04054 |
| C0030567 | Parkinson Disease | PLD1 | 5337 | phospholipase D1 | Q13393 |
| C0030567 | Parkinson Disease | PRKAA2 | 5563 | protein kinase AMP-activated catalytic subunit alpha 2 | P54646 |
| C0030567 | Parkinson Disease | PRNP | 5621 | prion protein | F7VJQ1 |
| C0030567 | Parkinson Disease | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C0030567 | Parkinson Disease | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0030567 | Parkinson Disease | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0030567 | Parkinson Disease | SHMT2 | 6472 | serine hydroxymethyltransferase 2 | P34897 |
| C0030567 | Parkinson Disease | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C0030567 | Parkinson Disease | TKT | 7086 | transketolase | P29401 |
| C0030567 | Parkinson Disease | CNTN2 | 6900 | contactin 2 | Q02246 |
| C0030567 | Parkinson Disease | ELOVL7 | 79993 | ELOVL fatty acid elongase 7 | A1L3X0 |
| C0030567 | Parkinson Disease | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0030567 | Parkinson Disease | DGKD | 8527 | diacylglycerol kinase delta | Q16760 |
| 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 |
