STX11

Syntaxin 11
Identifiers
Symbols	STX11 ; FHL4; HLH4; HPLH4
External IDs	Template:OMIM5 Template:MGI HomoloGene: 2792
Gene ontology Molecular function Template:GNF GO Template:GNF GO Template:GNF GO Cellular component Template:GNF GO Biological process Template:GNF GO Template:GNF GO
RNA expression pattern
File:PBB GE STX11 210190 at tn.png
More reference expression data
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

Syntaxin 11, also known as STX11, is a human gene.

Further reading

• Advani RJ, Bae HR, Bock JB; et al. (1998). "Seven novel mammalian SNARE proteins localize to distinct membrane compartments". J. Biol. Chem. 273 (17): 10317–24. PMID 9553086.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Tang BL, Low DY, Hong W (1998). "Syntaxin 11: a member of the syntaxin family without a carboxyl terminal transmembrane domain". Biochem. Biophys. Res. Commun. 245 (2): 627–32. doi:10.1006/bbrc.1998.8490. PMID 9571206.CS1 maint: Multiple names: authors list (link)
• Valdez AC, Cabaniols JP, Brown MJ, Roche PA (1999). "Syntaxin 11 is associated with SNAP-23 on late endosomes and the trans-Golgi network". J. Cell. Sci. 112 ( Pt 6): 845–54. PMID 10036234.CS1 maint: Multiple names: authors list (link)
• Martín-Martín B, Nabokina SM, Lazo PA, Mollinedo F (1999). "Co-expression of several human syntaxin genes in neutrophils and differentiating HL-60 cells: variant isoforms and detection of syntaxin 1". J. Leukoc. Biol. 65 (3): 397–406. PMID 10080545.CS1 maint: Multiple names: authors list (link)
• Roperch JP, Lethrone F, Prieur S; et al. (1999). "SIAH-1 promotes apoptosis and tumor suppression through a network involving the regulation of protein folding, unfolding, and trafficking: identification of common effectors with p53 and p21(Waf1)". Proc. Natl. Acad. Sci. U.S.A. 96 (14): 8070–3. PMID 10393949.CS1 maint: Explicit use of et al. (link) 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)
• 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)
• zur Stadt U, Schmidt S, Kasper B; et al. (2005). "Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11". Hum. Mol. Genet. 14 (6): 827–34. doi:10.1093/hmg/ddi076. PMID 15703195.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Stelzl U, Worm U, Lalowski M; et al. (2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell. 122 (6): 957–68. doi:10.1016/j.cell.2005.08.029. PMID 16169070.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Yamamoto K, Ishii E, Horiuchi H; et al. (2006). "Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people". J. Hum. Genet. 50 (11): 600–3. doi:10.1007/s10038-005-0293-1. PMID 16180048.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Rual JF, Venkatesan K, Hao T; et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Zur Stadt U, Beutel K, Kolberg S; et al. (2006). "Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A". Hum. Mutat. 27 (1): 62–8. doi:10.1002/humu.20274. PMID 16278825.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Bryceson YT, Rudd E, Zheng C; et al. (2007). "Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients". Blood. 110 (6): 1906–15. doi:10.1182/blood-2007-02-074468. PMID 17525286.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Arneson LN, Brickshawana A, Segovis CM; et al. (2007). "Cutting edge: syntaxin 11 regulates lymphocyte-mediated secretion and cytotoxicity". J. Immunol. 179 (6): 3397–401. PMID 17785771.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)