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DYT7 dystonia 7, torsion (autosomal dominant) [ Homo sapiens (human) ]

Gene ID: 1866, updated on 31-Aug-2024

Summary

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Official Symbol
DYT7provided by HGNC
Official Full Name
dystonia 7, torsion (autosomal dominant)provided by HGNC
Primary source
MIM:602124
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
18p

Bibliography

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Related articles in PubMed

  1. DYT7 gene locus for cervical dystonia on chromosome 18p is questionable. Winter P, et al. Mov Disord, 2012 Dec. PMID 23115116
  2. Genetics of psychiatric disease. Berrettini WH. Annu Rev Med, 2000. PMID 10774477
  3. Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution. Leube B, et al. Hum Mol Genet, 1996 Oct. PMID 8894706
  4. [Dystonia genes and elucidation of their roles in dystonia pathogenesis]. Kawarai T, et al. Rinsho Shinkeigaku, 2013. PMID 23782819

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
dystonia 7, torsion (autosomal dominant)
OMIM: 602124GeneReviews: Not available

General gene information

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Other Names

  • Dystonia-7 (torsion dystonia, adult-onset, focal)

Property

  • phenotype only

Gene LinkOut

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