URL of this page: https://medlineplus.gov/genetics/gene/atxn2/

ATXN2 gene

ataxin 2
From Genetics Home Reference. Learn more

Normal Function

The ATXN2 gene provides instructions for making a protein called ataxin-2. This protein is found throughout the body, but its function is unknown. Ataxin-2 is found in the fluid inside cells (cytoplasm) and seems to interact with a cell structure called the endoplasmic reticulum. The endoplasmic reticulum is involved in protein production, processing, and transport. Researchers believe that ataxin-2 may be involved in processing RNA, a chemical cousin of DNA. Ataxin-2 is also thought to play a role in the translation of genetic information to produce proteins.

One region of the ATXN2 gene contains a DNA segment known as a CAG trinucleotide repeat. This segment is made up of a series of three DNA building blocks (cytosine, adenine, and guanine) that appear multiple times in a row. Normally, the CAG segment is repeated approximately 22 times within the gene.

Health Conditions Related to Genetic Changes

Spinocerebellar ataxia type 2

Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. SCA2 results from a mutation in the ATXN2 gene known as a trinucleotide repeat expansion. This mutation increases the length of the repeated CAG segment in the ATXN2 gene. People with 32 or more repeats CAG repeats in the ATXN2 gene develop SCA2.

It is unclear how the abnormally long CAG segment affects the function of the ataxin-2 protein. The abnormal protein apparently leads to cell death, as people with SCA2 show a loss of brain cells. Certain brain cells called Purkinje cells seem to be particularly sensitive to the presence of abnormal ataxin-2. Purkinje cells are located in the part of the brain that coordinates movement (cerebellum) and are involved in chemical signaling between nerve cells (neurons). It is unknown how the abnormal ataxin-2 protein leads to the death of Purkinje and other brain cells. Over time, the loss of these cells causes the movement problems characteristic of SCA2.

More About This Health Condition

Amyotrophic lateral sclerosis

MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis

More About This Health Condition

Other Names for This Gene

  • ataxin-2
  • ATX2
  • ATX2_HUMAN
  • SCA2

Additional Information & Resources

Tests Listed in the Genetic Testing Registry

Scientific Articles on PubMed

Catalog of Genes and Diseases from OMIM

Research Resources

References

  • Lastres-Becker I, Rüb U, Auburger G. Spinocerebellar ataxia 2 (SCA2). Cerebellum. 2008;7(2):115-24. doi: 10.1007/s12311-008-0019-y. Review. Citation on PubMed
  • van de Loo S, Eich F, Nonis D, Auburger G, Nowock J. Ataxin-2 associates with rough endoplasmic reticulum. Exp Neurol. 2009 Jan;215(1):110-8. doi: 10.1016/j.expneurol.2008.09.020. Epub 2008 Oct 11. Citation on PubMed
  • Velázquez Pérez L, Cruz GS, Santos Falcón N, Enrique Almaguer Mederos L, Escalona Batallan K, Rodríguez Labrada R, Paneque Herrera M, Laffita Mesa JM, Rodríguez Díaz JC, Rodríguez RA, González Zaldivar Y, Coello Almarales D, Almaguer Gotay D, Jorge Cedeño H. Molecular epidemiology of spinocerebellar ataxias in Cuba: insights into SCA2 founder effect in Holguin. Neurosci Lett. 2009 Apr 24;454(2):157-60. doi: 10.1016/j.neulet.2009.03.015. Epub 2009 Mar 11. Citation on PubMed
From Genetics Home Reference

Genetics Home Reference has merged with MedlinePlus. Genetics Home Reference content now can be found in the "Genetics" section of MedlinePlus. Learn more

The resources on this site should not be used as a substitute for professional medical care or advice. Users with questions about a personal health condition should consult with a qualified healthcare professional.