| 1 | SCAR21, SCYL1
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| Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia.
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| Schmidt WM, Rutledge SL, Schüle R, Mayerhofer B, Züchner S, Boltshauser E, Bittner RE.
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| Am J Hum Genet 97(6):855-61. doi: 10.1016/j.ajhg.2015.10.011. Epub 2015 Nov 12.
2015
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| 2 | MCRS1, SCYL1, TERT
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| The 58-kda microspherule protein (MSP58) represses human telomerase reverse transcriptase (hTERT) gene expression and cell proliferation by interacting with telomerase transcriptional element-interacting factor (TEIF).
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| Hsu CC, Chen CH, Hsu TI, Hung JJ, Ko JL, Zhang B, Lee YC, Chen HK, Chang WC, Lin DY.
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| Biochim Biophys Acta 1843(3):565-79.
2014
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| 3 | CEP250, SCYL1
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| TEIF associated centrosome activity is regulated by EGF/PI3K/Akt signaling.
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| Zhao J, Zou Y, Liu H, Wang H, Zhang H, Hou W, Li X, Jia X, Zhang J, Hou L, Zhang B.
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| Biochim Biophys Acta 1843(9):1851-64. doi: 10.1016/j.bbamcr.2014.04.021. Epub 2014 Apr 25.
2014
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| 4 | SCYL1
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| Scyl1 scaffolds class II Arfs to specific subcomplexes of coatomer through the γ-COP appendage domain.
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| Hamlin JN, Schroeder LK, Fotouhi M, Dokainish H, Ioannou MS, Girard M, Summerfeldt N, Melançon P, McPherson PS.
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| J Cell Sci 127(Pt 7):1454-63. doi: 10.1242/jcs.136481. Epub 2014 Jan 30.
2014
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| 5 | SCYL1
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| An early onset progressive motor neuron disorder in Scyl1-deficient mice is associated with mislocalization of TDP-43.
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| Pelletier S, Gingras S, Howell S, Vogel P, Ihle JN.
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| J Neurosci 32(47):16560-73. doi: 10.1523/JNEUROSCI.1787-12.2012.
2012
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| 6 | SCYL1
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| Scyl1 facilitates nuclear tRNA export in mammalian cells by acting at the nuclear pore complex.
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| Chafe SC, Mangroo D.
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| Mol Biol Cell 21(14):2483-99. doi: 10.1091/mbc.E10-03-0176. Epub 2010 May 26.
2010
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| 7 | SCYL1
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| Scyl1 regulates Golgi morphology.
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| Burman JL, Hamlin JN, McPherson PS.
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| PLoS One 5(3):e9537. doi: 10.1371/journal.pone.0009537.
2010
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| 8 | SCYL1
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| Localization of TEIF in the centrosome and its functional association with centrosome amplification in DNA damage, telomere dysfunction and human cancers.
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| Gong Y, Sun Y, McNutt MA, Sun Q, Hou L, Liu H, Shen Q, Ling Y, Chi Y, Zhang B.
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| Oncogene 28(12):1549-60. Epub 2009 Feb 9.
2009
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| 9 | SCYL1
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| Scyl1, mutated in a recessive form of spinocerebellar neurodegeneration, regulates COPI-mediated retrograde traffic.
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| Burman JL, Bourbonniere L, Philie J, Stroh T, Dejgaard SY, Presley JF, McPherson PS.
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| J Biol Chem 283(33):22774-86. Epub 2008 Jun 13.
2008
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| 10 | SCAR21, SCYL1
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| Scyl1, mutated in a recessive form of spinocerebellar neurodegeneration, regulates COPI-mediated retrograde traffic.
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| Burman JL, Bourbonniere L, Philie J, Stroh T, Dejgaard SY, Presley JF, McPherson PS.
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| J Biol Chem 283(33):22774-86. doi: 10.1074/jbc.M801869200. Epub 2008 Jun 13. 2008
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| 11 | SCYL1
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| Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration.
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| Schmidt WM, Kraus C, Hoger H, Hochmeister S, Oberndorfer F, Branka M, Bingemann S, Lassmann H, Muller M, Macedo-Souza LI, Vainzof M, Zatz M, Reis A, Bittner RE.
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| EMBO Rep 8(7):691-7. Epub 2007 Jun 15. 2007
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| 12 | SCAR21, SCYL1
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| Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration.
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| Schmidt WM, Kraus C, Höger H, Hochmeister S, Oberndorfer F, Branka M, Bingemann S, Lassmann H, Müller M, Macedo-Souza LI, Vainzof M, Zatz M, Reis A, Bittner RE.
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| EMBO Rep 8(7):691-7. Epub 2007 Jun 15. 2007
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| 13 | 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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| 14 | SCYL1
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| Transcriptional upregulation of DNA polymerase beta by TEIF.
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| Zhao Y, Zheng J, Ling Y, Hou L, Zhang B.
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| Biochem Biophys Res Commun 333(3):908-16.
2005
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| 15 | GORAB, SCYL1
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| Cloning and characterization of a novel gene which encodes a protein interacting with the mitosis-associated kinase-like protein NTKL.
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| Di Y, Li J, Fang J, Xu Z, He X, Zhang F, Ling J, Li X, Xu D, Li L, Li YY, Huo K.
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| J Hum Genet 48(6):315-21. Epub 2003 May 29. 2003
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| 16 | SCYL1
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| Identification and Characterization of the Human Protein Kinase-like Gene NTKL: Mitosis-Specific Centrosomal Localization of an Alternatively Spliced Isoform.
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| Kato M, Yano Ki K, Morotomi-Yano K, Saito H, Miki Y.
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| Genomics 79(6):760-7. 2002
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| 17 | PCNXL3, MALAT1, RELA, TFEB, SCYL1
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| Construction of a 350-kb sequence-ready 11q13 cosmid contig encompassing the markers D11S4933 and D11S546: mapping of 11 genes and 3 tumor-associated translocation breakpoints.
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| van Asseldonk M, Schepens M, de Bruijn D, Janssen B, Merkx G, Geurts van Kessel A.
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| Genomics 66(1):35-42. 2000
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| 18 | SCYL1
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| Cloning and preliminary characterization of a 105 kDa protein with an N-terminal kinase-like domain.
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| Liu SC, Lane WS, Lienhard GE.
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| Biochim Biophys Acta 1517(1):148-52. 2000
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