From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
Exocyst complex component 6B is a protein that in humans is encoded by the EXOC6B gene .[ 5]
Function
In yeast and rat, Sec15 is part of a multiprotein complex that is required for targeted exocytosis .[ 5]
References
Further reading
Brymora A, Valova VA, Larsen MR, Roufogalis BD, Robinson PJ (August 2001). "The brain exocyst complex interacts with RalA in a GTP-dependent manner: identification of a novel mammalian Sec3 gene and a second Sec15 gene" . The Journal of Biological Chemistry . 276 (32): 29792–7. doi :10.1074/jbc.C100320200 . PMID 11406615 .
Feng S, Knödler A, Ren J, Zhang J, Zhang X, Hong Y, Huang S, Peränen J, Guo W (May 2012). "A Rab8 guanine nucleotide exchange factor-effector interaction network regulates primary ciliogenesis" . The Journal of Biological Chemistry . 287 (19): 15602–9. doi :10.1074/jbc.M111.333245 . PMC 3346093 . PMID 22433857 .
Wen J, Lopes F, Soares G, Farrell SA, Nelson C, Qiao Y, Martell S, Badukke C, Bessa C, Ylstra B, Lewis S, Isoherranen N, Maciel P, Rajcan-Separovic E (July 2013). "Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2" . Orphanet Journal of Rare Diseases . 8 : 100. doi :10.1186/1750-1172-8-100 . PMC 3710273 . PMID 23837398 . {{cite journal }}
: CS1 maint: unflagged free DOI (link )
Borsani G, Piovani G, Zoppi N, Bertini V, Bini R, Notarangelo L, Barlati S (2008). "Cytogenetic and molecular characterization of a de-novo t(2p;7p) translocation involving TNS3 and EXOC6B genes in a boy with a complex syndromic phenotype". European Journal of Medical Genetics . 51 (4): 292–302. doi :10.1016/j.ejmg.2008.02.006 . PMID 18424204 .
This article incorporates text from the United States National Library of Medicine , which is in the public domain .