RAB11FIP4

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RAB11 family interacting protein 4 (class II)
Identifiers
Symbol(s) RAB11FIP4; FLJ00131; KIAA1821; MGC11316; MGC126566; RAB11-FIP4
External IDs MGI: 2442920 HomoloGene: 8803
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 84440 268451
Ensembl ENSG00000131242 ENSMUSG00000017639
Uniprot Q86YS3 Q8BQP8
Refseq NM_032932 (mRNA)
NP_116321 (protein)		 NM_175543 (mRNA)
NP_780752 (protein)
Location Chr 17: 26.74 - 26.89 Mb Chr 11: 79.41 - 79.51 Mb
Pubmed search [1] [2]

RAB11 family interacting protein 4 (class II), also known as RAB11FIP4, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: RAB11FIP4 RAB11 family interacting protein 4 (class II).

[edit] Further reading

  • Jenne DE, Tinschert S, Stegmann E, et al. (2000). "A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions.". Genomics 66 (1): 93–7. doi:10.1006/geno.2000.6179. PMID 10843809. 
  • Nagase T, Nakayama M, Nakajima D, et al. (2001). "Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.". DNA Res. 8 (2): 85–95. PMID 11347906. 
  • Jenne DE, Tinschert S, Reimann H, et al. (2001). "Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions.". Am. J. Hum. Genet. 69 (3): 516–27. PMID 11468690. 
  • Wallace DM, Lindsay AJ, Hendrick AG, McCaffrey MW (2003). "Rab11-FIP4 interacts with Rab11 in a GTP-dependent manner and its overexpression condenses the Rab11 positive compartment in HeLa cells.". Biochem. Biophys. Res. Commun. 299 (5): 770–9. PMID 12470645. 
  • 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. 
  • Jenne DE, Tinschert S, Dorschner MO, et al. (2003). "Complete physical map and gene content of the human NF1 tumor suppressor region in human and mouse.". Genes Chromosomes Cancer 37 (2): 111–20. doi:10.1002/gcc.10206. PMID 12696059. 
  • 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. 
  • 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. 
  • Fielding AB, Schonteich E, Matheson J, et al. (2006). "Rab11-FIP3 and FIP4 interact with Arf6 and the exocyst to control membrane traffic in cytokinesis.". EMBO J. 24 (19): 3389–99. doi:10.1038/sj.emboj.7600803. PMID 16148947. 
  • Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.". Cell 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569. 
  • Douglas J, Cilliers D, Coleman K, et al. (2007). "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.". Nat. Genet. 39 (8): 963–5. doi:10.1038/ng2083. PMID 17632510. 
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