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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 |
|---|---|---|---|
| 7167 | TPI1 | triosephosphate isomerase 1 | |
| 7915 | ALDH5A1 | aldehyde dehydrogenase 5 family member A1 | |
| 7991 | TUSC3 | tumor suppressor candidate 3 | |
| 8050 | PDHX | pyruvate dehydrogenase complex component X | |
| 8398 | PLA2G6 | phospholipase A2 group VI | |
| 8560 | DEGS1 | delta 4-desaturase, sphingolipid 1 | |
| 8803 | SUCLA2 | succinate-CoA ligase ADP-forming subunit beta | |
| 8867 | SYNJ1 | synaptojanin 1 | |
| 8869 | ST3GAL5 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | |
| 9091 | PIGQ | phosphatidylinositol glycan anchor biosynthesis class Q |
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 |
