TGM6

From English Wikipedia @ Freddythechick

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Transglutaminase 6 is a protein that in humans is encoded by the TGM6 gene. [1]

Function and Clinical Significance

The protein encoded by this gene belongs to the transglutaminase superfamily. It catalyzes the cross-linking of proteins and the conjugation of polyamines to proteins. Mutations in this gene are associated with spinocerebellar ataxia type 35 (SCA35). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011].

Mutations in TGM6 cause acute myeloid leukaemia.[2] The presence of antibodies against TG6 is statistically related to gluten ataxia, amongst other conditions.

References

  1. ^ "Entrez Gene: Transglutaminase 6". Retrieved 2014-04-29.
  2. ^ Pan LL, Huang YM, Wang M, Zhuang XE, Luo DF, Guo SC, Zhang ZS, Huang Q, Lin SL, Wang SY (Feb 2015). "Positional cloning and next-generation sequencing identified a TGM6 mutation in a large Chinese pedigree with acute myeloid leukaemia". European Journal of Human Genetics. 23 (2): 218–23. doi:10.1038/ejhg.2014.67. PMC 4297898. PMID 24755948.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.