| 1 | KIF15, KIF18A, KIFBP
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| Kinesin-binding protein ensures accurate chromosome segregation by buffering KIF18A and KIF15.
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| Malaby HLH, Dumas ME, Ohi R, Stumpff J.
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| J Cell Biol 218(4):1218-1234. doi: 10.1083/jcb.201806195. Epub 2019 Feb 1.
2019
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| 2 | KIF15, KIFBP
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| Role of Kif15 and its novel mitotic partner KBP in K-fiber dynamics and chromosome alignment.
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| Brouwers N, Mallol Martinez N, Vernos I.
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| PLoS One 12(4):e0174819. doi: 10.1371/journal.pone.0174819. eCollection 2017.
2017
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| 3 | KIF3A, KIFBP
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| KIF1-binding protein interacts with KIF3A in haploid male germ cells.
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| Lehti MS, Kotaja N, Sironen A.
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| Reproduction 150(3):209-16. doi: 10.1530/REP-15-0173. 2015
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| 4 | KIFBP
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| Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria.
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| Valence S, Poirier K, Lebrun N, Saillour Y, Sonigo P, Bessières B, Attié-Bitach T, Benachi A, Masson C, Encha-Razavi F, Chelly J, Bahi-Buisson N.
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| Neurogenetics 14(3-4):215-24. doi: 10.1007/s10048-013-0373-x. Epub 2013 Sep 27. 2013
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| 5 | GOSHS, KIFBP
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| KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome.
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| Drévillon L, Megarbane A, Demeer B, Matar C, Benit P, Briand-Suleau A, Bodereau V, Ghoumid J, Nasser M, Decrouy X, Doco-Fenzy M, Rustin P, Gaillard D, Goossens M, Giurgea I.
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| Hum Mol Genet 22(12):2387-99. doi: 10.1093/hmg/ddt083. Epub 2013 Feb 19. 2013
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| 6 | GOSHS, KIFBP, STMN2
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| KBP interacts with SCG10, linking Goldberg-Shprintzen syndrome to microtubule dynamics and neuronal differentiation.
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| Alves MM, Burzynski G, Delalande JM, Osinga J, van der Goot A, Dolga AM, de Graaff E, Brooks AS, Metzger M, Eisel UL, Shepherd I, Eggen BJ, Hofstra RM.
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| Hum Mol Genet 19(18):3642-51. Epub 2010 Jul 9.PMID: 20621975 2010
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| 7 | KIFBP, STMN2
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| Mutations in SCG10 are not involved in Hirschsprung disease.
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| Alves MM, Osinga J, Verheij JB, Metzger M, Eggen BJ, Hofstra RM.
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| PLoS One 5(12):e15144.PMID: 21187955 2010
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| 8 | DEL1P36, DEL21QT, DEL4Q, DEL6QD, DUP2PD, EOMES, GOSHS, KIFBP, MPAC, RAB3GAP1, WARBM1
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| Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.
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| Dobyns WB, Mirzaa G, Christian SL, Petras K, Roseberry J, Clark GD, Curry CJ, McDonald-McGinn D, Medne L, Zackai E, Parsons J, Zand DJ, Hisama FM, Walsh CA, Leventer RJ, Martin CL, Gajecka M, Shaffer LG.
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| Am J Med Genet A 146A(13):1637-54. 2008
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| 9 | GOSHS, KIFBP
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| KBP is essential for axonal structure, outgrowth and maintenance in zebrafish, providing insight into the cellular basis of Goldberg-Shprintzen syndrome.
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| Lyons DA, Naylor SG, Mercurio S, Dominguez C, Talbot WS.
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| Development 135(3):599-608.PMID: 18192286 2008
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| 10 | GOSHS, KIFBP
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| Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systems.
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| Brooks AS, Bertoli-Avella AM, Burzynski GM, Breedveld GJ, Osinga J, Boven LG, Hurst JA, Mancini GM, Lequin MH, de Coo RF, Matera I, de Graaff E, Meijers C, Willems PJ, Tibboel D, Oostra BA, Hofstra RM.
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| Am J Hum Genet 77(1):120-6. Epub 2005 May 9. 2005
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| 11 | KIF1B, KIFBP
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| The novel protein KBP regulates mitochondria localization by interaction with a kinesin-like protein.
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| Wozniak MJ, Melzer M, Dorner C, Haring HU, Lammers R.
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| BMC Cell Biol 6:35. 2005
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| 12 | ASAP1, ASAP2, BIRC6, ERBIN, INTS2, KIAA1239, KIAA1244, KIAA1257, KIAA1370, KIAA1462, KIAA1467, KIAA1539, KIAA1949, KIFBP, MED23, MTUS1, PLEKHG1, PLEKHH1, RNF150, SERINC2, UVSSA, VANGL2, WWC3, XPO5, XPO7, ZDHHC8, ZMIZ1, ZNF512B
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| Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
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| Nagase T, Ishikawa K, Kikuno R, Hirosawa M, Nomura N, Ohara O.
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| DNA Res 6(5):337-45. 1999
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