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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
movement disease
Summary
- Definition
- A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity.
- Super Class
- brain disease
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2629 | GBA1 | glucosylceramidase beta 1 | |
| 2639 | GCDH | glutaryl-CoA dehydrogenase | |
| 2752 | GLUL | glutamate-ammonia ligase | |
| 3073 | HEXA | hexosaminidase subunit alpha | |
| 3251 | HPRT1 | hypoxanthine phosphoribosyltransferase 1 | |
| 4125 | MAN2B1 | mannosidase alpha class 2B member 1 | |
| 4967 | OGDH | oxoglutarate dehydrogenase | |
| 5048 | PAFAH1B1 | platelet activating factor acetylhydrolase 1b regulatory subunit 1 | |
| 5160 | PDHA1 | pyruvate dehydrogenase E1 subunit alpha 1 | |
| 5373 | PMM2 | phosphomannomutase 2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O00754 | Lysosomal alpha-mannosidase | |
| O15305 | Phosphomannomutase 2 | |
| O95427 | GPI ethanolamine phosphate transferase 1 | |
| P00387 | NADH-cytochrome b5 reductase 3 | |
| P00492 | Hypoxanthine-guanine phosphoribosyltransferase | |
| P04062 | Lysosomal acid glucosylceramidase | |
| P04156 | Major prion protein | |
| P05177 | Cytochrome P450 1A2 | |
| P06865 | Beta-hexosaminidase subunit alpha | |
| P07602 | Prosaposin |
