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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 |
|---|---|---|---|
| 5160 | PDHA1 | pyruvate dehydrogenase E1 subunit alpha 1 | |
| 5279 | PIGC | phosphatidylinositol glycan anchor biosynthesis class C | |
| 5290 | PIK3CA | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | |
| 5660 | PSAP | prosaposin | |
| 5728 | PTEN | phosphatase and tensin homolog | |
| 5973 | RENBP | renin binding protein | |
| 6342 | SCP2 | sterol carrier protein 2 | |
| 6389 | SDHA | succinate dehydrogenase complex flavoprotein subunit A | |
| 6392 | SDHD | succinate dehydrogenase complex subunit D | |
| 6487 | ST3GAL3 | ST3 beta-galactoside alpha-2,3-sialyltransferase 3 |
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 |
