SAMD9

From Wikipedia, the free encyclopedia


Sterile alpha motif domain containing 9
Identifiers
Symbol(s) SAMD9; C7orf5; FLJ20073; KIAA2004; NFTC; OEF1; OEF2
External IDs OMIM: 610456 HomoloGene: 75072
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 54809 n/a
Ensembl ENSG00000205413 n/a
Uniprot Q5K651 n/a
Refseq NM_017654 (mRNA)
NP_060124 (protein)		 n/a (mRNA)
n/a (protein)
Location Chr 7: 92.57 - 92.59 Mb n/a
Pubmed search [1] n/a

Sterile alpha motif domain containing 9, also known as SAMD9, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: SAMD9 sterile alpha motif domain containing 9.

[edit] Further reading

  • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1-2): 171–4. PMID 8125298. 
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1-2): 149–56. PMID 9373149. 
  • "Toward a complete human genome sequence." (1999). Genome Res. 8 (11): 1097–108. PMID 9847074. 
  • 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. 
  • Hillier LW, Fulton RS, Fulton LA, et al. (2003). "The DNA sequence of human chromosome 7.". Nature 424 (6945): 157–64. doi:10.1038/nature01782. PMID 12853948. 
  • 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. 
  • 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. 
  • Topaz O, Indelman M, Chefetz I, et al. (2006). "A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis.". Am. J. Hum. Genet. 79 (4): 759–64. doi:10.1086/508069. PMID 16960814. 
  • Li CF, MacDonald JR, Wei RY, et al. (2007). "Human sterile alpha motif domain 9, a novel gene identified as down-regulated in aggressive fibromatosis, is absent in the mouse.". BMC Genomics 8: 92. doi:10.1186/1471-2164-8-92. PMID 17407603. 
  • Dereure O (2007). "[SAMD9 mutation in normophosphatemic familial tumoral calcinosis]". Annales de dermatologie et de vénéréologie 134 (5 Pt 1): 505. PMID 17507861. 
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