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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
dystonia
Summary
- Synonym
-
- dystonic disease
- Definition
- A movement disease that is characterized by involuntary muscle contractions causing repetitive or twisting movements.
- Super Class
- movement disease
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2821 | GPI | glucose-6-phosphate isomerase | |
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 3251 | HPRT1 | hypoxanthine phosphoribosyltransferase 1 | |
| 3340 | NDST1 | N-deacetylase and N-sulfotransferase 1 | |
| 4191 | MDH2 | malate dehydrogenase 2 | |
| 4329 | ALDH6A1 | aldehyde dehydrogenase 6 family member A1 | |
| 4594 | MMUT | methylmalonyl-CoA mutase | |
| 5048 | PAFAH1B1 | platelet activating factor acetylhydrolase 1b regulatory subunit 1 | |
| 5095 | PCCA | propionyl-CoA carboxylase subunit alpha | |
| 5096 | PCCB | propionyl-CoA carboxylase subunit beta |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9H9P8 | L-2-hydroxyglutarate dehydrogenase, mitochondrial | |
| Q9NZ01 | Very-long-chain enoyl-CoA reductase | |
| Q9P2R7 | Succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial | |
| Q9UKM7 | Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase | |
| Q9UNP4 | Lactosylceramide alpha-2,3-sialyltransferase |
