FAM127A

From Wikipedia, the free encyclopedia


Family with sequence similarity 127, member A
Identifiers
Symbol(s) FAM127A; CXX1; MAR8C; MART8C; MGC117411; Mar8; Mart8
External IDs OMIM: 300213
Orthologs
Human Mouse
Entrez 8933 n/a


Refseq NM_003928 (mRNA)
NP_003919 (protein)		 n/a (mRNA)
n/a (protein)
Pubmed search [1] n/a

Family with sequence similarity 127, member A, also known as FAM127A, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: FAM127A family with sequence similarity 127, member A.

[edit] Further reading

  • Andersson B, Wentland MA, Ricafrente JY, et al. (1996). "A "double adaptor" method for improved shotgun library construction.". Anal. Biochem. 236 (1): 107–13. doi:10.1006/abio.1996.0138. PMID 8619474. 
  • Yu W, Andersson B, Worley KC, et al. (1997). "Large-scale concatenation cDNA sequencing.". Genome Res. 7 (4): 353–8. PMID 9110174. 
  • Frattini A, Faranda S, Zucchi I, Vezzoni P (1998). "A low-copy repeat in Xq26 represents a novel putatively prenylated protein gene (CXX1) and its pseudogenes (DXS9914, DXS9915, and DXS9916).". Genomics 46 (1): 167–9. doi:10.1006/geno.1997.5006. PMID 9403077. 
  • 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. 
  • 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. 
  • Brandt J, Schrauth S, Veith AM, et al. (2005). "Transposable elements as a source of genetic innovation: expression and evolution of a family of retrotransposon-derived neogenes in mammals.". Gene 345 (1): 101–11. doi:10.1016/j.gene.2004.11.022. PMID 15716091. 
  • 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. 
  • Brandt J, Veith AM, Volff JN (2005). "A family of neofunctionalized Ty3/gypsy retrotransposon genes in mammalian genomes.". Cytogenet. Genome Res. 110 (1-4): 307–17. doi:10.1159/000084963. PMID 16093683. 
  • 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. 
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