Torsin A

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Torsin-1A (TorA) also known as dystonia 1 protein (DYT1) is a protein that in humans is encoded by the TOR1A gene (also known as DQ2 or DYT1).[5] TorA localizes to the endoplasmic reticulum and contiguous perinuclear space, where its ATPase activity is activated by either LULL1 or LAP1, respectively.

AliasesTOR1A, DQ2, DYT1, Torsin A, torsin family 1 member A, AMC5
End129,824,244 bp[1]
Quick facts TOR1A, Identifiers ...
TOR1A
Identifiers
AliasesTOR1A, DQ2, DYT1, Torsin A, torsin family 1 member A, AMC5
External IDsOMIM: 605204; MGI: 1353568; HomoloGene: 37263; GeneCards: TOR1A; OMA:TOR1A - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000113

NM_144884

RefSeq (protein)

NP_000104

NP_659133

Location (UCSC)Chr 9: 129.81 – 129.82 MbChr 2: 30.85 – 30.86 Mb
PubMed search[3][4]
Wikidata
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Function

The protein encoded by this gene is a member of the AAA family of adenosine triphosphatases (ATPases), is related to the Clp protease/heat shock family.[6]

Clinical significance

Mutations in this gene result in the autosomal dominant disorder, torsion dystonia 1.[6]

References

Further reading

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