Citations for
1SCA11, TTBK2
Spinocerebellar ataxia type 11-associated alleles of Ttbk2 dominantly interfere with ciliogenesis and cilium stability.
Bowie E, Norris R, Anderson KV, Goetz SC.
PLoS Genet 14(12):e1007844. doi: 10.1371/journal.pgen.1007844. eCollection 2018 Dec. 2018
2TTBK1, TTBK2
Pathological phosphorylation of tau and TDP-43 by TTBK1 and TTBK2 drives neurodegeneration.
Taylor LM, McMillan PJ, Liachko NF, Strovas TJ, Ghetti B, Bird TD, Keene CD, Kraemer BC.
Mol Neurodegener 13(1):7. doi: 10.1186/s13024-018-0237-9. 2018
3GRIK2, TTBK2
Tau Tubulin Kinase TTBK2 Sensitivity of Glutamate Receptor GluK2.
Nieding K, Matschke V, Meuth SG, Lang F, Seebohm G, Strutz-Seebohm N.
Cell Physiol Biochem 39(4):1444-52. doi: 10.1159/000447847. Epub 2016 Sep 9. 2016
4MCRS1, TTBK2
MCRS1 associates with cytoplasmic dynein and mediates pericentrosomal material recruitment.
Lee SH, Lee MS, Choi TI, Hong H, Seo JY, Kim CH, Kim J.
Sci Rep 6:27284. doi: 10.1038/srep27284. 2016
5KIF2A, MAPRE1, MAPRE1, TTBK2
TTBK2 with EB1/3 regulates microtubule dynamics in migrating cells through KIF2A phosphorylation.
Watanabe T, Kakeno M, Matsui T, Sugiyama I, Arimura N, Matsuzawa K, Shirahige A, Ishidate F, Nishioka T, Taya S, Hoshino M, Kaibuchi K.
J Cell Biol 210(5):737-51. doi: 10.1083/jcb.201412075. 2015
6TTBK2
TTBK2: a tau protein kinase beyond tau phosphorylation.
Liao JC, Yang TT, Weng RR, Kuo CT, Chang CW.
Biomed Res Int 2015:575170. doi: 10.1155/2015/575170. Epub 2015 Apr 9. Review. 2015
7CEP164, CEP97, TTBK2
Binding to Cep164, but not EB1, is essential for centriolar localization of TTBK2 and its function in ciliogenesis.
Oda T, Chiba S, Nagai T, Mizuno K.
Genes Cells 19(12):927-40. doi: 10.1111/gtc.12191. Epub 2014 Oct 9. 2014
8ALS10, TARDBP, TTBK1, TTBK2
The tau tubulin kinases TTBK1/2 promote accumulation of pathological TDP-43.
Liachko NF, McMillan PJ, Strovas TJ, Loomis E, Greenup L, Murrell JR, Ghetti B, Raskind MA, Montine TJ, Bird TD, Leverenz JB, Kraemer BC.
PLoS Genet LoS Genet. 2014 2014
9CEP164, TTBK2
Cep164 triggers ciliogenesis by recruiting Tau tubulin kinase 2 to the mother centriole.
Čajánek L, Nigg EA.
Proc Natl Acad Sci U S A 111(28):E2841-50. doi: 10.1073/pnas.1401777111. Epub 2014 Jun 30. 2014
10CCP110, TTBK2
TTBK2 kinase: linking primary cilia and cerebellar ataxias.
Jackson PK.
Cell 151(4):697-699. doi: 10.1016/j.cell.2012.10.027. 2012
11CCP110, SCA11, TTBK2
The spinocerebellar ataxia-associated gene Tau tubulin kinase 2 controls the initiation of ciliogenesis.
Goetz SC, Liem KF Jr, Anderson KV.
Cell 151(4):847-858. doi: 10.1016/j.cell.2012.10.010. 2012
12SCA11, TTBK2
TTBK2 kinase substrate specificity and the impact of spinocerebellar-ataxia-causing mutations on expression, activity, localization and development.
Bouskila M, Esoof N, Gay L, Fang EH, Deak M, Begley MJ, Cantley LC, Prescott A, Storey KG, Alessi DR.
Biochem J 437(1):157-67. 2011
13SCA11, TTBK2
Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds.
Bauer P, Stevanin G, Beetz C, Synofzik M, Schmitz-Hübsch T, Wüllner U, Berthier E, Ollagnon-Roman E, Riess O, Forlani S, Mundwiller E, Durr A, Schöls L, Brice A.
J Neurol Neurosurg Psychiatry 81(11):1229-32. doi: 10.1136/jnnp.2009.202150. Epub 2010 Jul 28. 2010
14SCA11, TTBK2
Spinocerebellar ataxia type 11 in the Chinese Han population.
Xu Q, Li X, Wang J, Yi J, Lei L, Shen L, Jiang H, Xia K, Pan Q, Tang B.
Neurol Sci 31(1):107-9. doi: 10.1007/s10072-009-0129-4. Epub 2009 Sep 19. 2010
15SCA11, TTBK2
Missense exchanges in the TTBK2 gene mutated in SCA11.
Edener U, Kurth I, Meiner A, Hoffmann F, Hübner CA, Bernard V, Gillessen-Kaesbach G, Zühlke C.
J Neurol 256(11):1856-9. Epub 2009 Jun 17. 2009
16TTBK2, SCA11
Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
Houlden H, Johnson J, Gardner-Thorpe C, Lashley T, Hernandez D, Worth P, Singleton AB, Hilton DA, Holton J, Revesz T, Davis MB, Giunti P, Wood NW.
Nat Genet 39(12):1434-6. Epub 2007 Nov 25. 2007
17TTBK2
Expression, purification and crystallization of a human tau-tubulin kinase 2 that phosphorylates tau protein.
Kitano-Takahashi M, Morita H, Kondo S, Tomizawa K, Kato R, Tanio M, Shirota Y, Takahashi H, Sugio S, Kohno T.
Acta Crystallogr Sect F Struct Biol Cryst Commun 63(Pt 7):602-4. Epub 2007 Jun 15. 2007
18CDAN1, STARD9, TTBK2, VPS39
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H,Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Cretien A,Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rossler J, Le Merrer M, YanivI, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H.
Am J Hum Genet 71(6):1467-74. Epub 2002 Nov 14. 2002