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DYT17 dystonia 17 [ Homo sapiens (human) ]

Gene ID: 100216344, updated on 31-Aug-2024

Summary

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Official Symbol
DYT17provided by HGNC
Official Full Name
dystonia 17provided by HGNC
Primary source
MIM:612406
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:
20p11.22-q13.12

Bibliography

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Related articles in PubMed

  1. A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22-q13.12. Chouery E, et al. Neurogenetics, 2008 Oct. PMID 18688663

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
dystonia 17
OMIM: 612406GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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