SAMD9

SAMD9
Identifiers
Aliases	SAMD9, C7orf5, DRIF1, NFTC, OEF1, OEF2, sterile alpha motif domain containing 9, MIRAGE
External IDs	HomoloGene: 75072 GeneCards: SAMD9
Gene location (Human)
Chr.	Chromosome 7 (human)[1]
End	93,118,023 bp[1]
RNA expression pattern
	; ;
	More reference expression data
Gene ontology
Molecular function	• protein binding;
Cellular component	• cytoplasm; • intracellular membrane-bounded organelle; • cytosol; • early endosome;
Biological process	• endosomal vesicle fusion;
	Sources:Amigo / QuickGO
Orthologs
	54809
	n/a
	ENSG00000205413
	n/a
	Q5K651
	n/a
	NM_017654; NM_001193307
	n/a
	NP_001180236; NP_060124
	n/a
	Wikidata
View/Edit Human

Sterile alpha motif domain-containing protein 9 is a protein that in humans is encoded by the SAMD9 gene.^[3]

References

Maruyama K, Sugano S (January 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (October 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
"Toward a complete human genome sequence". Genome Research. 8 (11): 1097–108. November 1998. doi:10.1101/gr.8.11.1097. PMID 9847074.
Topaz O, Indelman M, Chefetz I, Geiger D, Metzker A, Altschuler Y, Choder M, Bercovich D, Uitto J, Bergman R, Richard G, Sprecher E (October 2006). "A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis". American Journal of Human Genetics. 79 (4): 759–64. doi:10.1086/508069. PMC 1592555. PMID 16960814.
Li CF, MacDonald JR, Wei RY, Ray J, Lau K, Kandel C, Koffman R, Bell S, Scherer SW, Alman BA (April 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.
Dereure O (May 2007). "[SAMD9 mutation in normophosphatemic familial tumoral calcinosis]". Annales De Dermatologie Et De Venereologie. 134 (5 Pt 1): 505. doi:10.1016/S0151-9638(07)89230-1. PMID 17507861.

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