1 | KIF1C, SPAX2
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| Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.
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| Yücel-Yılmaz D, Yücesan E, Yalnızoğlu D, Oğuz KK, Sağıroğlu MŞ, Özbek U, Serdaroğlu E, Bilgiç B, Erdem S, İşeri SAU, Hanağası H, Gürvit H, Özgül RK, Dursun A.
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| Brain Dev 40(6):458-464. doi: 10.1016/j.braindev.2018.02.013. Epub 2018 Mar 12.
2018
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2 | KIF1A, KIF1C, KIF21B, KIF5B, KIF9
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| Microtubule motors involved in nuclear movement during skeletal muscle differentiation.
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| Gache V, Gomes ER, Cadot B.
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| Mol Biol Cell 28(7):865-874. doi: 10.1091/mbc.E16-06-0405. Epub 2017 Feb 8.
2017
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3 | KIF1C, RAB6A
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| Rab6 regulation of the kinesin family KIF1C motor domain contributes to Golgi tethering.
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| Lee PL, Ohlson MB, Pfeffer SR.
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| Elife 4. doi: 10.7554/eLife.06029.
2015
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4 | KIF1C
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| Podosome-regulating kinesin KIF1C translocates to the cell periphery in a CLASP-dependent manner.
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| Efimova N, Grimaldi A, Bachmann A, Frye K, Zhu X, Feoktistov A, Straube A, Kaverina I.
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| J Cell Sci 127(Pt 24):5179-88. doi: 10.1242/jcs.149633. Epub 2014 Oct 24.
2014
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5 | ARL6IP1, ARSI, ERLIN1, FLRT1, KIF1C, PGAP1, RAB3GAP2, SPAX2, SPG59, SPG60, SPG61, SPG62, SPG66, SPG67, SPG68, SPG69, SPG71, USP8, WDR48, ZFR
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| Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.
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| Novarino G, Fenstermaker AG, Zaki MS, Hofree M, Silhavy JL, Heiberg AD, Abdellateef M, Rosti B, Scott E, Mansour L, Masri A, Kayserili H, Al-Aama JY, Abdel-Salam GMH, Karminejad A, Kara M, Kara B, Bozorgmehri B, Ben-Omran T, Mojahedi F, El Din Mahmoud IG, Bouslam N, Bouhouche A, Benomar A, Hanein S, Raymond L, Forlani S, Mascaro M, Selim L, Shehata N, Al-Allawi N, Bindu PS, Azam M, Gunel M, Caglayan A, Bilguvar K, Tolun A, Issa MY, Schroth J, Spencer EG, Rosti RO, Akizu N, Vaux KK, Johansen A, Koh AA, Megahed H, Durr A, Brice A, Stevanin G, Gabriel SB, Ideker T, Gleeson JG.
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| Science 343(6170):506-511. doi: 10.1126/science.1247363.
2014
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6 | KIF1C, SPAX2
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| KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction.
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| Dor T, Cinnamon Y, Raymond L, Shaag A, Bouslam N, Bouhouche A, Gaussen M, Meyer V, Durr A, Brice A, Benomar A, Stevanin G, Schuelke M, Edvardson S.
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| J Med Genet 51(2):137-42. doi: 10.1136/jmedgenet-2013-102012. Epub 2013 Dec 6.
2014
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7 | KIF1C, SPAX2
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| KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction.
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| Dor T, Cinnamon Y, Raymond L, Shaag A, Bouslam N, Bouhouche A, Gaussen M, Meyer V, Durr A, Brice A, Benomar A, Stevanin G, Schuelke M, Edvardson S.
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| J Med Genet 51(2):137-42. doi: 10.1136/jmedgenet-2013-102012. Epub 2013 Dec 6.
2014
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8 | KIF1C
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| Directional persistence of migrating cells requires Kif1C-mediated stabilization of trailing adhesions.
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| Theisen U, Straube E, Straube A.
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| Dev Cell 23(6):1153-66. doi: 10.1016/j.devcel.2012.11.005.
2012
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9 | KIF1C
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| Identification of Orch3, a locus controlling dominant resistance to autoimmune orchitis, as kinesin family member 1C.
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| del Rio R, McAllister RD, Meeker ND, Wall EH, Bond JP, Kyttaris VC, Tsokos GC, Tung KS, Teuscher C.
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| PLoS Genet 8(12):e1003140. doi: 10.1371/journal.pgen.1003140. Epub 2012 Dec 27.
2012
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10 | KIF1A, KIF1B, KIF1C
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| The kinesin-1 motor protein is regulated by a direct interaction of its head and tail.
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| Dietrich KA, Sindelar CV, Brewer PD, Downing KH, Cremo CR, Rice SE.
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| Proc Natl Acad Sci U S A 105(26):8938-43. Epub 2008 Jun 25. 2008
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11 | ABL2, AKAP8, ANKRD13D, AP3D1, ARFGAP3, ARMCX6, ASUN, BAT2L, BCl2L13, BNIP3L, BPTF, BRD7, BZW1, BZW2, C12orf43, C19orf26, C1orf105, C2orf49, C6orf81, CA10, CAD, CARHSP1, CBX4, CCDC55, CCDC61, CCNK, CDC42BPB, CDC42EP3, CDC42EP4, CDS2, CENPN, CLK1, COPA, CSDA, CTPS2, DBN1, DCP1A, DECR2, DPF2, DPM1, EIF2AK1, EPB41L4A, EPN1, FAM91A1, FOSL2, FOXK1, GDF5OS, GFOD2, GIGYF2, GPATCH8, GTPBP1, HES7, HNRNPUL1, KIF1C, LPIN2, LRCH4, MAN2C1, MAST1, MED13, MED24, MED26, MINK1, MISP, MYO10, NKTR, OSBP, PAM, PCDH7, PEX14, PHF16, PHRF1, PLCB4, PLXNC1, POM121, POM121L2, PPHLN1, PRICKLE3, PRX, PUM2, RABGGTB, RBEL1, RIMS1, RIMS2, RPL14, RRP1B, RRP8, SAFB, SCAMP3, SCMH1, SCYL1, SENP6, SERBP1, SFRS13A, SFRS17A, SIPA1L1, SLC26A6, SLIRP, SLMAP, SNTA1, SORBS3, SPICE1, SSFA2, STAM, SUB1, TFIP11, TLN2, TMC6, TMEM104, TMEM106B, TMEM22, TOM1, UHRF1, UTP14A, WDR43, ZNF324, ZNF648
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| Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.
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| Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M.
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| Cell. 127(3):635-48. 2006
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12 | KIF1C
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| The kinesin KIF1C and microtubule plus ends regulate podosome dynamics in macrophages.
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| Kopp P, Lammers R, Aepfelbacher M, Woehlke G, Rudel T, Machuy N, Steffen W, Linder S.
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| Mol Biol Cell 17(6):2811-23. Epub 2006 Mar 22. 2006
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13 | KIF1C
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| Molecular motor KIF1C is not essential for mouse survival and motor-dependent retrograde Golgi apparatus-to-endoplasmic reticulum transport.
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| Nakajima K, Takei Y, Tanaka Y, Nakagawa T, Nakata T, Noda Y, Setou M, Hirokawa N.
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| Mol Cell Biol. 22(3):866-73. 2002
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14 | KIF1C
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| Characterization of KIF1C, a new kinesin-like protein involved in vesicle transport from the Golgi apparatus to the endoplasmic reticulum.
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| Dorner C, Ciossek T, Muller S, Moller PH, Ullrich A, Lammers R.
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| J Biol Chem 273(32):20267-75. 1998
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15 | AATK, ACIN1, ACOT11, ACSBG1, ADAMTS4, ADGRV1, AKAP11, ANKLE2, ARHGAP26, ARHGEF2, ASTN2, ATP2C2, ATP9A, BICD2, BZRAP1, C12orf51, CAND2, CEP135, CLASP1, CLASP2, CLUAP1, CLUH, CNOT3, COBL, CPNE3, CRTC1, CRY2, CSTF2T, CUL3, CUL4B, DAAM1, DAGLA, DEPDC5, DNAJC13, DOCK10, DZIP3, FBXW11, FKBP15, G3BP2, HEPH, HIP1R, HIPK1, ICOSLG, KIAA0649, KIAA0652, KIF13B, KIF1C, KIF21A, L3MBTL1, LDB3, MAGI2, MAP4K4, MFAP3L, MGEA5, MRC2, MTMR4, N4BP1, NPHP4, OBSL1, PAN2, PHACTR2, PHF2, PHLDB1, PLXND1, PPFIA3, PTCD1, RAB11FIP3, RBM19, RICH2, RNF40, RNF8, ROCK2, RRP12, SAPS2, SETX, SIN3B, SLC24A1, SMCHD1, SNAP91, SOCS5, SS18L1, SWAP70, TBC1D9B, TELO2, TNRC15, TSC22D2, UBE4B, UHRF1BP1L, ULK2, ZBED4, ZC3H11A, ZNF623
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| Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.
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| Ishikawa K, Nagase T, Suyama M, Miyajima N, Tanaka A, Kotani H, Nomura N,Ohara O.
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| DNA Res 5(3):169-76. 1998
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