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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 |
|---|---|---|---|
| 1737 | DLAT | dihydrolipoamide S-acetyltransferase | |
| 1738 | DLD | dihydrolipoamide dehydrogenase | |
| 1800 | DPEP1 | dipeptidase 1 | |
| 1892 | ECHS1 | enoyl-CoA hydratase, short chain 1 | |
| 2571 | GAD1 | glutamate decarboxylase 1 | |
| 2583 | B4GALNT1 | beta-1,4-N-acetyl-galactosaminyltransferase 1 | |
| 2629 | GBA1 | glucosylceramidase beta 1 | |
| 2639 | GCDH | glutaryl-CoA dehydrogenase | |
| 2720 | GLB1 | galactosidase beta 1 | |
| 2760 | GM2A | ganglioside GM2 activator |
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 |
