SEPT11
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| Septin 11 | |||||||||||||
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| Identifiers | |||||||||||||
| Symbols | SEPT11; | ||||||||||||
| External IDs | OMIM: 612887 MGI: 1277214 HomoloGene: 56800 GeneCards: SEPT11 Gene | ||||||||||||
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| Orthologs | |||||||||||||
| Species | Human | Mouse | |||||||||||
| Entrez | 55752 | 52398 | |||||||||||
| Ensembl | ENSG00000138758 | ENSMUSG00000058013 | |||||||||||
| UniProt | Q9NVA2 | Q3TBA0 | |||||||||||
| RefSeq (mRNA) | NM_018243 | NM_001009818.1 | |||||||||||
| RefSeq (protein) | NP_060713 | NP_001009818.1 | |||||||||||
| Location (UCSC) | Chr 4: 77.87 – 77.96 Mb |
Chr 5: 93.52 – 93.61 Mb |
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| PubMed search | [1] | [2] | |||||||||||
Septin-11 is a protein that in humans is encoded by the SEPT11 gene.[1][2][3]
[edit] References
- ^ Kojima K, Sakai I, Hasegawa A, Niiya H, Azuma T, Matsuo Y, Fujii N, Tanimoto M, Fujita S (Apr 2004). "FLJ10849, a septin family gene, fuses MLL in a novel leukemia cell line CNLBC1 derived from chronic neutrophilic leukemia in transformation with t(4;11)(q21;q23)". Leukemia 18 (5): 998–1005. doi:10.1038/sj.leu.2403334. PMID 14999297.
- ^ Kim DS, Hubbard SL, Peraud A, Salhia B, Sakai K, Rutka JT (May 2004). "Analysis of mammalian septin expression in human malignant brain tumors". Neoplasia 6 (2): 168–78. doi:10.1593/neo.03310. PMC 1502092. PMID 15140406. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1502092.
- ^ "Entrez Gene: SEPT11 septin 11". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55752.
[edit] Further reading
- Andersen JS, Lyon CE, Fox AH, et al. (2002). "Directed proteomic analysis of the human nucleolus.". Curr. Biol. 12 (1): 1–11. doi:10.1016/S0960-9822(01)00650-9. PMID 11790298.
- Wistow G, Bernstein SL, Wyatt MK, et al. (2002). "Expressed sequence tag analysis of human RPE/choroid for the NEIBank Project: over 6000 non-redundant transcripts, novel genes and splice variants.". Mol. Vis. 8: 205–20. PMID 12107410.
- 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. PMC 139241. PMID 12477932. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=139241.
- Gevaert K, Goethals M, Martens L, et al. (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides.". Nat. Biotechnol. 21 (5): 566–9. doi:10.1038/nbt810. PMID 12665801.
- 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.
- Hanai N, Nagata K, Kawajiri A, et al. (2004). "Biochemical and cell biological characterization of a mammalian septin, Sept11.". FEBS Lett. 568 (1-3): 83–8. doi:10.1016/j.febslet.2004.05.030. PMID 15196925.
- 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.
- 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. PMC 528928. PMID 15489334. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=528928.
- Andersen JS, Lam YW, Leung AK, et al. (2005). "Nucleolar proteome dynamics.". Nature 433 (7021): 77–83. doi:10.1038/nature03207. PMID 15635413.
- Sudo K, Ito H, Iwamoto I, et al. (2007). "SEPT9 sequence alternations causing hereditary neuralgic amyotrophy are associated with altered interactions with SEPT4/SEPT11 and resistance to Rho/Rhotekin-signaling.". Hum. Mutat. 28 (10): 1005–13. doi:10.1002/humu.20554. PMID 17546647.
- Xin X, Pache M, Zieger B, et al. (2007). "Septin expression in proliferative retinal membranes.". J. Histochem. Cytochem. 55 (11): 1089–94. doi:10.1369/jhc.7A7188.2007. PMID 17625225.
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