CYFIP1

From Wikipedia, the free encyclopedia


Cytoplasmic FMR1 interacting protein 1
Identifiers
Symbol(s) CYFIP1; FLJ45151; P140SRA-1; SHYC
External IDs OMIM: 606322 MGI: 1338801 HomoloGene: 22628
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 23191 20430
Ensembl ENSG00000068793 ENSMUSG00000030447
Refseq NM_001033028 (mRNA)
NP_001028200 (protein)		 NM_011370 (mRNA)
NP_035500 (protein)
Location Chr 15: 20.44 - 20.56 Mb Chr 7: 55.71 - 55.8 Mb
Pubmed search [1] [2]

Cytoplasmic FMR1 interacting protein 1, also known as CYFIP1, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: CYFIP1 cytoplasmic FMR1 interacting protein 1.

[edit] Further reading

  • Nomura N, Nagase T, Miyajima N, et al. (1995). "Prediction of the coding sequences of unidentified human genes. II. The coding sequences of 40 new genes (KIAA0041-KIAA0080) deduced by analysis of cDNA clones from human cell line KG-1.". DNA Res. 1 (5): 223-9. PMID 7584044. 
  • Kobayashi K, Kuroda S, Fukata M, et al. (1998). "p140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase.". J. Biol. Chem. 273 (1): 291-5. PMID 9417078. 
  • Witke W, Podtelejnikov AV, Di Nardo A, et al. (1998). "In mouse brain profilin I and profilin II associate with regulators of the endocytic pathway and actin assembly.". EMBO J. 17 (4): 967-76. doi:10.1093/emboj/17.4.967. PMID 9463375. 
  • Schenck A, Bardoni B, Moro A, et al. (2001). "A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P.". Proc. Natl. Acad. Sci. U.S.A. 98 (15): 8844-9. doi:10.1073/pnas.151231598. PMID 11438699. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932. 
  • Chai JH, Locke DP, Greally JM, et al. (2003). "Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons.". Am. J. Hum. Genet. 73 (4): 898-925. PMID 14508708. 
  • Brajenovic M, Joberty G, Küster B, et al. (2004). "Comprehensive proteomic analysis of human Par protein complexes reveals an interconnected protein network.". J. Biol. Chem. 279 (13): 12804-11. doi:10.1074/jbc.M312171200. PMID 14676191. 
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40-5. doi:10.1038/ng1285. PMID 14702039. 
  • Innocenti M, Zucconi A, Disanza A, et al. (2004). "Abi1 is essential for the formation and activation of a WAVE2 signalling complex.". Nat. Cell Biol. 6 (4): 319-27. doi:10.1038/ncb1105. PMID 15048123. 
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi:10.1101/gr.2596504. PMID 15489334. 
  • Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173-8. doi:10.1038/nature04209. PMID 16189514. 
  • Kawano Y, Yoshimura T, Tsuboi D, et al. (2005). "CRMP-2 is involved in kinesin-1-dependent transport of the Sra-1/WAVE1 complex and axon formation.". Mol. Cell. Biol. 25 (22): 9920-35. doi:10.1128/MCB.25.22.9920-9935.2005. PMID 16260607. 
  • Bittel DC, Kibiryeva N, Butler MG (2006). "Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.". Pediatrics 118 (4): e1276-83. doi:10.1542/peds.2006-0424. PMID 16982806. 
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