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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 |
|---|---|---|---|
| 43 | ACHE | acetylcholinesterase (Yt blood group) | |
| 51 | ACOX1 | acyl-CoA oxidase 1 | |
| 126 | ADH1C | alcohol dehydrogenase 1C (class I), gamma polypeptide | |
| 175 | AGA | aspartylglucosaminidase | |
| 410 | ARSA | arylsulfatase A | |
| 523 | ATP6V1A | ATPase H+ transporting V1 subunit A | |
| 1312 | COMT | catechol-O-methyltransferase | |
| 1593 | CYP27A1 | cytochrome P450 family 27 subfamily A member 1 | |
| 1629 | DBT | dihydrolipoamide branched chain transacylase E2 | |
| 1727 | CYB5R3 | cytochrome b5 reductase 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 |
