SAMD9

SAMD9
Identifiers
Aliases	SAMD9, C7orf5, DRIF1, NFTC, OEF1, OEF2, sterile alpha motif domain containing 9, MIRAGE, M7MLS2
External IDs	OMIM: 610456; HomoloGene: 75072; GeneCards: SAMD9; OMA:SAMD9 - orthologs
Gene location (Human) Chr. Chromosome 7 (human) Band 7q21.2 Start 93,099,513 bp End 93,118,023 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in amniotic fluid oral cavity buccal mucosa cell mucosa of pharynx gums gingival epithelium palpebral conjunctiva decidua epithelium of nasopharynx trabecular bone n/a More reference expression data BioGPS 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 Species Human Mouse Entrez 54809 n/a Ensembl ENSG00000205413 n/a UniProt Q5K651 n/a RefSeq (mRNA) NM_017654 NM_001193307 n/a RefSeq (protein) NP_001180236 NP_060124 n/a Location (UCSC) Chr 7: 93.1 – 93.12 Mb n/a PubMed search 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.

Further reading

• 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.
• Sanger Centre, The; Washington University Genome Sequencing Cente, The (November 1998). "Toward a complete human genome sequence". Genome Research. 8 (11): 1097–108. 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.{{cite journal}}: CS1 maint: unflagged free DOI (link)
• 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.