CXorf40A

From Wikipedia, the free encyclopedia


Chromosome X open reading frame 40A
Identifiers
Symbol(s) CXorf40A; CXorf40; EOLA1
External IDs MGI: 1915868 HomoloGene: 12274
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 91966 68618
Ensembl ENSG00000197620 ENSMUSG00000045237
Uniprot Q8TE69 Q3TDX9
Refseq NM_178124 (mRNA)
NP_835225 (protein)		 XM_001005393 (mRNA)
XP_001005393 (protein)
Location Chr X: 148.43 - 148.44 Mb Chr X: 66.65 - 66.65 Mb
Pubmed search [1] [2]

Chromosome X open reading frame 40A, also known as CXorf40A, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: CXorf40A chromosome X open reading frame 40A.

[edit] Further reading

  • 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. 
  • Liang Z, Yang Z (2005). "Identification and characterization of a novel gene EOLA1 stimulating ECV304 cell proliferation.". Biochem. Biophys. Res. Commun. 325 (3): 798-802. doi:10.1016/j.bbrc.2004.10.124. PMID 15541360. 
  • 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. 
  • Hinz T, Allam A, Wesch D, et al. (2000). "Cell-surface expression of transrearranged Vgamma-cbeta T-cell receptor chains in healthy donors and in ataxia telangiectasia patients.". Br. J. Haematol. 109 (1): 201-10. PMID 10848801. 
  • Timms KM, Bondeson ML, Ansari-Lari MA, et al. (1997). "Molecular and phenotypic variation in patients with severe Hunter syndrome.". Hum. Mol. Genet. 6 (3): 479-86. PMID 9147653. 
  • Timms KM, Lu F, Shen Y, et al. (1996). "130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus.". Genome Res. 5 (1): 71-8. PMID 8717057. 
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