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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 |
|---|---|---|---|---|---|
| C4721453 | Peripheral Nervous System Diseases | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C4721453 | Peripheral Nervous System Diseases | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
| C4721453 | Peripheral Nervous System Diseases | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C4721453 | Peripheral Nervous System Diseases | ECHS1 | 1892 | enoyl-CoA hydratase, short chain 1 | P30084 |
| C4721453 | Peripheral Nervous System Diseases | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C4721453 | Peripheral Nervous System Diseases | GAS1 | 2619 | growth arrest specific 1 | P54826 |
| C4721453 | Peripheral Nervous System Diseases | GFRA1 | 2674 | GDNF family receptor alpha 1 | P56159 |
| C4721453 | Peripheral Nervous System Diseases | ALOX15 | 246 | arachidonate 15-lipoxygenase | P16050 |
| C4721453 | Peripheral Nervous System Diseases | HADHA | 3030 | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | P40939 |
| C4721453 | Peripheral Nervous System Diseases | HADH | 3033 | hydroxyacyl-CoA dehydrogenase | Q16836 |
| C4721453 | Peripheral Nervous System Diseases | HADHB | 3032 | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | P55084 |
| C4721453 | Peripheral Nervous System Diseases | MTM1 | 4534 | myotubularin 1 | Q13496 |
| C4721453 | Peripheral Nervous System Diseases | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C4721453 | Peripheral Nervous System Diseases | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C4721453 | Peripheral Nervous System Diseases | PRNP | 5621 | prion protein | F7VJQ1 |
| C4721453 | Peripheral Nervous System Diseases | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
| C4721453 | Peripheral Nervous System Diseases | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C4721453 | Peripheral Nervous System Diseases | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C4721453 | Peripheral Nervous System Diseases | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
| C4721453 | Peripheral Nervous System Diseases | MTMR2 | 8898 | myotubularin related protein 2 | Q13614 |
| C0031117 | Peripheral Neuropathy | ST3GAL4 | 6484 | ST3 beta-galactoside alpha-2,3-sialyltransferase 4 | Q11206 |
| C0031117 | Peripheral Neuropathy | GLA | 2717 | galactosidase alpha | P06280 |
| C0031117 | Peripheral Neuropathy | ARSA | 410 | arylsulfatase A | P15289 |
| C0031117 | Peripheral Neuropathy | PMM2 | 5373 | phosphomannomutase 2 | O15305 |
| C0031117 | Peripheral Neuropathy | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
