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SCA20 spinocerebellar ataxia 20 [ Homo sapiens (human) ]

Gene ID: 407973, updated on 31-Aug-2024

Summary

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Official Symbol
SCA20provided by HGNC
Official Full Name
spinocerebellar ataxia 20provided by HGNC
Primary source
MIM:608687
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
DUP11q12; C11DUPq12

Genomic context

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Location:
11q12

Bibliography

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Related articles in PubMed

  1. Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5. Lorenzo DN, et al. Neurology, 2006 Dec 12. PMID 17159129
  2. Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20. Knight MA, et al. Brain, 2004 May. PMID 14998916
  3. A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20. Knight MA, et al. Hum Mol Genet, 2008 Dec 15. PMID 18801880, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
spinocerebellar ataxia 20
OMIM: 608687GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

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Research Materials