RASSF8

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Ras association (RalGDS/AF-6) domain family 8
PDB rendering based on 2cs4.
Available structures: 2cs4
Identifiers
Symbol(s) RASSF8; C12orf2; HoJ-1
External IDs OMIM: 608231 MGI: 1918573 HomoloGene: 5219
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 11228 71323
Ensembl ENSG00000123094 ENSMUSG00000030259
Uniprot Q8NHQ8 Q149Q5
Refseq NM_007211 (mRNA)
NP_009142 (protein)		 NM_027760 (mRNA)
NP_082036 (protein)
Location Chr 12: 26 - 26.12 Mb Chr 6: 145.77 - 145.77 Mb
Pubmed search [1] [2]

Ras association (RalGDS/AF-6) domain family 8, also known as RASSF8, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: RASSF8 Ras association (RalGDS/AF-6) domain family 8.

[edit] Further reading

  • Falvella FS, Spinola M, Manenti G, et al. (2007). "Common polymorphisms in D12S1034 flanking genes RASSF8 and BHLHB3 are not associated with lung adenocarcinoma risk.". Lung Cancer 56 (1): 1-7. doi:10.1016/j.lungcan.2006.11.008. PMID 17194498. 
  • Falvella FS, Manenti G, Spinola M, et al. (2006). "Identification of RASSF8 as a candidate lung tumor suppressor gene.". Oncogene 25 (28): 3934-8. doi:10.1038/sj.onc.1209422. PMID 16462760. 
  • 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. 
  • 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. 
  • Jin J, Smith FD, Stark C, et al. (2004). "Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization.". Curr. Biol. 14 (16): 1436-50. doi:10.1016/j.cub.2004.07.051. PMID 15324660. 
  • 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. 
  • Debeer P, Schoenmakers EF, Twal WO, et al. (2002). "The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly.". J. Med. Genet. 39 (2): 98-104. PMID 11836357. 
  • Debeer P, Schoenmakers EF, Thoelen R, et al. (2000). "Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint.". Eur. J. Hum. Genet. 8 (8): 561-70. doi:10.1038/sj.ejhg.5200497. PMID 10951517. 
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