CHMP2B

From Wikipedia, the free encyclopedia


Chromatin modifying protein 2B
Identifiers
Symbol(s) CHMP2B; DMT1; CHMP2.5; DKFZP564O123; VPS2-2
External IDs OMIM: 609512 HomoloGene: 8534
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 25978 n/a
Ensembl ENSG00000083937 n/a
Uniprot Q9UQN3 n/a
Refseq NM_014043 (mRNA)
NP_054762 (protein)		 n/a (mRNA)
n/a (protein)
Location Chr 3: 87.36 - 87.39 Mb n/a
Pubmed search [1] n/a

Chromatin modifying protein 2B, also known as CHMP2B, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: CHMP2B chromatin modifying protein 2B.

[edit] Further reading

  • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1-2): 171-4. PMID 8125298. 
  • Brown J, Ashworth A, Gydesen S, et al. (1996). "Familial non-specific dementia maps to chromosome 3.". Hum. Mol. Genet. 4 (9): 1625-8. PMID 8541850. 
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1-2): 149-56. PMID 9373149. 
  • Ashworth A, Lloyd S, Brown J, et al. (1999). "Molecular genetic characterisation of frontotemporal dementia on chromosome 3.". Dementia and geriatric cognitive disorders 10 Suppl 1: 93-101. PMID 10436350. 
  • Lai CH, Chou CY, Ch'ang LY, et al. (2000). "Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics.". Genome Res. 10 (5): 703-13. PMID 10810093. 
  • Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.". Genome Res. 11 (3): 422-35. doi:10.1101/gr.154701. PMID 11230166. 
  • Simpson JC, Wellenreuther R, Poustka A, et al. (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing.". EMBO Rep. 1 (3): 287-92. doi:10.1093/embo-reports/kvd058. PMID 11256614. 
  • Howard TL, Stauffer DR, Degnin CR, Hollenberg SM (2002). "CHMP1 functions as a member of a newly defined family of vesicle trafficking proteins.". J. Cell. Sci. 114 (Pt 13): 2395-404. PMID 11559748. 
  • 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. 
  • Strack B, Calistri A, Craig S, et al. (2003). "AIP1/ALIX is a binding partner for HIV-1 p6 and EIAV p9 functioning in virus budding.". Cell 114 (6): 689-99. PMID 14505569. 
  • von Schwedler UK, Stuchell M, Müller B, et al. (2003). "The protein network of HIV budding.". Cell 114 (6): 701-13. PMID 14505570. 
  • Martin-Serrano J, Yarovoy A, Perez-Caballero D, et al. (2003). "Divergent retroviral late-budding domains recruit vacuolar protein sorting factors by using alternative adaptor proteins.". Proc. Natl. Acad. Sci. U.S.A. 100 (21): 12414-9. doi:10.1073/pnas.2133846100. PMID 14519844. 
  • 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. 
  • Kelleher T, Ryan E, Barrett S, et al. (2005). "DMT1 genetic variability is not responsible for phenotype variability in hereditary hemochromatosis.". Blood Cells Mol. Dis. 33 (1): 35-9. doi:10.1016/j.bcmd.2004.04.005. PMID 15223008. 
  • 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. 
  • Takeuchi K, Bjarnason I, Laftah AH, et al. (2005). "Expression of iron absorption genes in mouse large intestine.". Scand. J. Gastroenterol. 40 (2): 169-77. doi:10.1080/00365520510011489. PMID 15764147. 
  • Skibinski G, Parkinson NJ, Brown JM, et al. (2005). "Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia.". Nat. Genet. 37 (8): 806-8. doi:10.1038/ng1609. PMID 16041373. 
  • 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. 
  • Cannon A, Baker M, Boeve B, et al. (2006). "CHMP2B mutations are not a common cause of frontotemporal lobar degeneration.". Neurosci. Lett. 398 (1-2): 83-4. doi:10.1016/j.neulet.2005.12.056. PMID 16431024. 
  • Nousiainen M, Silljé HH, Sauer G, et al. (2006). "Phosphoproteome analysis of the human mitotic spindle.". Proc. Natl. Acad. Sci. U.S.A. 103 (14): 5391-6. doi:10.1073/pnas.0507066103. PMID 16565220. 
 This article on a gene on chromosome 3 is a stub. You can help Wikipedia by expanding it.