TTBK2
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An Error has occurred retrieving Wikidata item for infobox Tau tubulin kinase 2 is a protein in humans that is encoded by the TTBK2 gene.[1] This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11); a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem.[2]
References
- ↑ "Entrez Gene: Tau tubulin kinase 2". Retrieved 2012-06-11.
- ↑ Houlden H, Johnson J, Gardner-Thorpe C, Lashley T, Hernandez D, Worth P, et al. (December 2007). "Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11". Nature Genetics. 39 (12): 1434–1436. doi:10.1038/ng.2007.43. PMID 18037885. S2CID 20774216.
Further reading
- Edener U, Kurth I, Meiner A, Hoffmann F, Hübner CA, Bernard V, et al. (November 2009). "Missense exchanges in the TTBK2 gene mutated in SCA11". Journal of Neurology. 256 (11): 1856–1859. doi:10.1007/s00415-009-5209-0. PMID 19533200. S2CID 10343192.
- Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, et al. (December 2002). "Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1". American Journal of Human Genetics. 71 (6): 1467–1474. doi:10.1086/344781. PMC 378595. PMID 12434312.
- Worth PF, Giunti P, Gardner-Thorpe C, Dixon PH, Davis MB, Wood NW (August 1999). "Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3". American Journal of Human Genetics. 65 (2): 420–426. doi:10.1086/302495. PMC 1377940. PMID 10417284.
- Kitano-Takahashi M, Morita H, Kondo S, Tomizawa K, Kato R, Tanio M, et al. (July 2007). "Expression, purification and crystallization of a human tau-tubulin kinase 2 that phosphorylates tau protein". Acta Crystallographica. Section F, Structural Biology and Crystallization Communications. 63 (Pt 7): 602–604. doi:10.1107/S1744309107028783. PMC 2335129. PMID 17620722.
- Xu Q, Li X, Wang J, Yi J, Lei L, Shen L, et al. (February 2010). "Spinocerebellar ataxia type 11 in the Chinese Han population". Neurological Sciences. 31 (1): 107–109. doi:10.1007/s10072-009-0129-4. PMID 19768375. S2CID 972027.
- Houlden H, Johnson J, Gardner-Thorpe C, Lashley T, Hernandez D, Worth P, et al. (December 2007). "Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11". Nature Genetics. 39 (12): 1434–1436. doi:10.1038/ng.2007.43. PMID 18037885. S2CID 20774216.
- Chen Z, Puzriakova A, Houlden H (October 2019) [July 2008]. "Spinocerebellar Ataxia Type 11". In Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A (eds.). GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle. PMID 20301723.
- Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, et al. (May 2004). "Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families". Archives of Neurology. 61 (5): 727–733. doi:10.1001/archneur.61.5.727. PMID 15148151.
- Crockett DK, Fillmore GC, Elenitoba-Johnson KS, Lim MS (April 2005). "Analysis of phosphatase and tensin homolog tumor suppressor interacting proteins by in vitro and in silico proteomics". Proteomics. 5 (5): 1250–1262. doi:10.1002/pmic.200401046. PMID 15717329. S2CID 45130615.
