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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 |
|---|---|---|---|
| 57462 | MYORG | myogenesis regulating glycosidase (putative) | |
| 64116 | SLC39A8 | solute carrier family 39 member 8 | |
| 79143 | MBOAT7 | membrane bound O-acyltransferase domain containing 7 | |
| 79944 | L2HGDH | L-2-hydroxyglutarate dehydrogenase | |
| 79947 | DHDDS | dehydrodolichyl diphosphate synthase subunit | |
| 80055 | PGAP1 | post-GPI attachment to proteins inositol deacylase 1 | |
| 81562 | LMAN2L | lectin, mannose binding 2 like | |
| 113612 | CYP2U1 | cytochrome P450 family 2 subfamily U member 1 | |
| 148789 | B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 | |
| 197322 | ACSF3 | acyl-CoA synthetase family member 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 |
