BRWD3

From Wikipedia, the free encyclopedia


Bromodomain and WD repeat domain containing 3
Identifiers
Symbol(s) BRWD3; BRODL; FLJ38568
External IDs OMIM: 300553 MGI: 3029414 HomoloGene: 18736
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 254065 382236
Ensembl ENSG00000165288 ENSMUSG00000063663
Refseq NM_153252 (mRNA)
NP_694984 (protein)		 XM_897902 (mRNA)
XP_902995 (protein)
Location Chr X: 79.81 - 79.95 Mb Chr X: 104.95 - 105.04 Mb
Pubmed search [1] [2]

Bromodomain and WD repeat domain containing 3, also known as BRWD3, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: BRWD3 bromodomain and WD repeat domain containing 3.

[edit] Further reading

  • Field M, Tarpey PS, Smith R, et al. (2007). "Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly.". Am. J. Hum. Genet. 81 (2): 367–74. doi:10.1086/520677. PMID 17668385. 
  • Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.". Cell 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983. 
  • Müller P, Kuttenkeuler D, Gesellchen V, et al. (2005). "Identification of JAK/STAT signalling components by genome-wide RNA interference.". Nature 436 (7052): 871–5. doi:10.1038/nature03869. PMID 16094372. 
  • Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome.". Nature 434 (7031): 325–37. doi:10.1038/nature03440. PMID 15772651. 
  • Kalla C, Nentwich H, Schlotter M, et al. (2005). "Translocation t(X;11)(q13;q23) in B-cell chronic lymphocytic leukemia disrupts two novel genes.". Genes Chromosomes Cancer 42 (2): 128–43. doi:10.1002/gcc.20131. PMID 15543602. 
  • 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. 
  • 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. 
  • 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. 
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