SEPT9

Septin 9
Identifiers
Symbols	SEPT9 ; MSF; AF17q25; KIAA0991; MSF1; NAPB; PNUTL4; SINT1
External IDs	Template:OMIM5 Template:MGI HomoloGene: 4838
Gene ontology Molecular function Template:GNF GO Template:GNF GO Template:GNF GO Template:GNF GO Cellular component Template:GNF GO Template:GNF GO Template:GNF GO Template:GNF GO Template:GNF GO Biological process Template:GNF GO Template:GNF GO Template:GNF GO Template:GNF GO
Orthologs
Template:GNF Ortholog box
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a

Septin 9, also known as SEPT9, is a human gene.

Further reading

• Pellegrino JE, George RA, Biegel J; et al. (1998). "Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25". Hum. Genet. 101 (3): 277–83. PMID 9439655.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Nagase T, Ishikawa K, Suyama M; et al. (1999). "Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Res. 6 (1): 63–70. PMID 10231032.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Osaka M, Rowley JD, Zeleznik-Le NJ (1999). "MSF (MLL septin-like fusion), a fusion partner gene of MLL, in a therapy-related acute myeloid leukemia with a t(11;17)(q23;q25)". Proc. Natl. Acad. Sci. U.S.A. 96 (11): 6428–33. PMID 10339604.CS1 maint: Multiple names: authors list (link)
• Taki T, Ohnishi H, Shinohara K; et al. (1999). "AF17q25, a putative septin family gene, fuses the MLL gene in acute myeloid leukemia with t(11;17)(q23;q25)". Cancer Res. 59 (17): 4261–5. PMID 10485469.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Medina M, Marinescu RC, Overhauser J, Kosik KS (2000). "Hemizygosity of delta-catenin (CTNND2) is associated with severe mental retardation in cri-du-chat syndrome". Genomics. 63 (2): 157–64. doi:10.1006/geno.1999.6090. PMID 10673328.CS1 maint: Multiple names: authors list (link)
• Kalikin LM, Sims HL, Petty EM (2000). "Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors". Genomics. 63 (2): 165–72. doi:10.1006/geno.1999.6077. PMID 10673329.CS1 maint: Multiple names: authors list (link)
• Russell SE, McIlhatton MA, Burrows JF; et al. (2000). "Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors". Cancer Res. 60 (17): 4729–34. PMID 10987277.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• McIlhatton MA, Burrows JF, Donaghy PG; et al. (2001). "Genomic organization, complex splicing pattern and expression of a human septin gene on chromosome 17q25.3". Oncogene. 20 (41): 5930–9. doi:10.1038/sj.onc.1204752. PMID 11593400.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Yamamoto K, Shibata F, Yamaguchi M, Miura O (2003). "Fusion of MLL and MSF in adult de novo acute myelomonocytic leukemia (M4) with t(11;17)(q23;q25)". Int. J. Hematol. 75 (5): 503–7. PMID 12095151.CS1 maint: Multiple names: authors list (link)
• Surka MC, Tsang CW, Trimble WS (2003). "The mammalian septin MSF localizes with microtubules and is required for completion of cytokinesis". Mol. Biol. Cell. 13 (10): 3532–45. doi:10.1091/mbc.E02-01-0042. PMID 12388755.CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Nagata K, Kawajiri A, Matsui S; et al. (2003). "Filament formation of MSF-A, a mammalian septin, in human mammary epithelial cells depends on interactions with microtubules". J. Biol. Chem. 278 (20): 18538–43. doi:10.1074/jbc.M205246200. PMID 12626509.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Beausoleil SA, Jedrychowski M, Schwartz D; et al. (2004). "Large-scale characterization of HeLa cell nuclear phosphoproteins". Proc. Natl. Acad. Sci. U.S.A. 101 (33): 12130–5. doi:10.1073/pnas.0404720101. PMID 15302935.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Nagata K, Asano T, Nozawa Y, Inagaki M (2005). "Biochemical and cell biological analyses of a mammalian septin complex, Sept7/9b/11". J. Biol. Chem. 279 (53): 55895–904. doi:10.1074/jbc.M406153200. PMID 15485874.CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Scott M, Hyland PL, McGregor G; et al. (2005). "Multimodality expression profiling shows SEPT9 to be overexpressed in a wide range of human tumours". Oncogene. 24 (29): 4688–700. doi:10.1038/sj.onc.1208574. PMID 15782116.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Ito H, Iwamoto I, Morishita R; et al. (2005). "Possible role of Rho/Rhotekin signaling in mammalian septin organization". Oncogene. 24 (47): 7064–72. doi:10.1038/sj.onc.1208862. PMID 16007136.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Scott M, McCluggage WG, Hillan KJ; et al. (2006). "Altered patterns of transcription of the septin gene, SEPT9, in ovarian tumorigenesis". Int. J. Cancer. 118 (5): 1325–9. doi:10.1002/ijc.21486. PMID 16161048.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Kuhlenbäumer G, Hannibal MC, Nelis E; et al. (2005). "Mutations in SEPT9 cause hereditary neuralgic amyotrophy". Nat. Genet. 37 (10): 1044–6. doi:10.1038/ng1649. PMID 16186812.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)