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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 |
|---|---|---|---|
| 43 | ACHE | acetylcholinesterase (Yt blood group) | |
| 50 | ACO2 | aconitase 2 | |
| 501 | ALDH7A1 | aldehyde dehydrogenase 7 family member A1 | |
| 1544 | CYP1A2 | cytochrome P450 family 1 subfamily A member 2 | |
| 1589 | CYP21A2 | cytochrome P450 family 21 subfamily A member 2 | |
| 1717 | DHCR7 | 7-dehydrocholesterol reductase | |
| 1727 | CYB5R3 | cytochrome b5 reductase 3 | |
| 1836 | SLC26A2 | solute carrier family 26 member 2 | |
| 2350 | FOLR2 | folate receptor beta | |
| 2539 | G6PD | glucose-6-phosphate dehydrogenase |
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 |
