SAMD9

Sterile alpha motif domain containing 9
Identifiers
Symbols	SAMD9; C7orf5; DRIF1; FLJ20073; KIAA2004; NFTC; OEF1; OEF2
External IDs	OMIM: 610456 HomoloGene: 75072 GeneCards: SAMD9 Gene
Gene Ontology Cellular component • cytoplasm Sources: Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	54809	n/a
Ensembl	ENSG00000205413	n/a
UniProt	Q5K651	n/a
RefSeq (mRNA)	NM_001193307.1	n/a
RefSeq (protein)	NP_001180236.1	n/a
Location (UCSC)	Chr 7: 92.73 – 92.75 Mb	n/a
PubMed search	[1]	n/a

Sterile alpha motif domain-containing protein 9 is a protein that in humans is encoded by the SAMD9 gene.

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): 171–174. doi:10.1016/0378-1119(94)90802-8. 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): 149–156. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149. 
• "Toward a complete human genome sequence". Genome Res. 8 (11): 1097–108. 1999. doi:10.1101/gr.8.11.1097. 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): 16899–16903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=139241. 
• Scherer SW, Cheung J, MacDonald JR et al (2003). "Human chromosome 7: DNA sequence and biology". Science 300 (5620): 767–772. doi:10.1126/science.1083423. PMC 2882961. PMID 12690205. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2882961. 
• Hillier LW, Fulton RS, Fulton LA et al (2003). "The DNA sequence of human chromosome 7". Nature 424 (6945): 157–164. 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): 40–45. 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): 2121–2127. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=528928. 
• 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): 759–764. doi:10.1086/508069. PMC 1592555. PMID 16960814. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1592555. 
• 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. PMC 1855325. PMID 17407603. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1855325. 
• Dereure O (2007). "[SAMD9 mutation in normophosphatemic familial tumoral calcinosis]". Annales de dermatologie et de vénéréologie 134 (5 Pt 1): 505–505. doi:10.1016/S0151-9638(07)89230-1. PMID 17507861.