C7orf11

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Chromosome 7 open reading frame 11
Identifiers
Symbol(s) C7orf11; ABHS; ORF20; TTDN1
External IDs OMIM: 609188 MGI: 1913558 HomoloGene: 32633
Orthologs
Human Mouse
Entrez 136647 66308
Ensembl ENSG00000168303 n/a
Uniprot Q8TAP9 n/a
Refseq NM_138701 (mRNA)
NP_619646 (protein)		 NM_025479 (mRNA)
NP_079755 (protein)
Location Chr 7: 40.14 - 40.14 Mb n/a
Pubmed search [1] [2]

Chromosome 7 open reading frame 11, also known as C7orf11, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: C7orf11 chromosome 7 open reading frame 11.

[edit] Further reading

  • Nakabayashi K, Fernandez BA, Teshima I, et al. (2002). "Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome.". Genomics 79 (2): 186–96. doi:10.1006/geno.2002.6695. PMID 11829489. 
  • 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. 
  • Scherer SW, Cheung J, MacDonald JR, et al. (2003). "Human chromosome 7: DNA sequence and biology.". Science 300 (5620): 767–72. doi:10.1126/science.1083423. PMID 12690205. 
  • 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. 
  • Nakabayashi K, Amann D, Ren Y, et al. (2005). "Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy.". Am. J. Hum. Genet. 76 (3): 510–6. doi:10.1086/428141. PMID 15645389. 
  • Beausoleil SA, Villén J, Gerber SA, et al. (2006). "A probability-based approach for high-throughput protein phosphorylation analysis and site localization.". Nat. Biotechnol. 24 (10): 1285–92. doi:10.1038/nbt1240. PMID 16964243. 
  • Botta E, Offman J, Nardo T, et al. (2007). "Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationships.". Hum. Mutat. 28 (1): 92–6. doi:10.1002/humu.20419. PMID 16977596. 
  • 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. 
  • Zhang Y, Tian Y, Chen Q, et al. (2007). "TTDN1 is a Plk1-interacting protein involved in maintenance of cell cycle integrity.". Cell. Mol. Life Sci. 64 (5): 632–40. doi:10.1007/s00018-007-6501-8. PMID 17310276. 
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