Kalpana Kalpana (Editor)

Ataxin 3

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Species
  
Entrez
  
4287

Human
  
Ensembl
  
ENSG00000066427

Ataxin 3

Aliases
  
ATXN3, AT3, ATX3, JOS, MJD, MJD1, SCA3, Ataxin 3

External IDs
  
MGI: 1099442 HomoloGene: 3658 GeneCards: ATXN3

Ataxin-3 is a protein that in humans is encoded by the ATXN3 gene.

Contents

Clinical significance

Machado-Joseph disease, also known as spinocerebellar ataxia-3, is an autosomal dominant neurologic disorder. The protein encoded by the ATXN3 gene contains (CAG)n repeats in the coding region, and the expansion of these repeats from the normal 13-36 to 68-79 is the cause of Machado-Joseph disease. There is an inverse correlation between the age of onset and CAG repeat numbers. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.

Interactions

Ataxin 3 has been shown to interact with:

  • RAD23A,
  • RAD23B, and
  • VCP.
  • Model organisms

    Model organisms have been used in the study of ATXN3 function. A conditional knockout mouse line called Atxn3tm1a(KOMP)Wtsi was generated at the Wellcome Trust Sanger Institute. Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion. Additional screens performed: - In-depth immunological phenotyping - in-depth bone and cartilage phenotyping

    References

    Ataxin 3 Wikipedia


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