CELSR3
Cadherin EGF LAG seven-pass G-type receptor 3is aproteinthat in humans is encoded by theCELSR3gene.[5][6]
The protein encoded by this gene is a member of the flamingo subfamily, part of the cadherin superfamily. The flamingo subfamily consists of nonclassic-type cadherins; a subpopulation that does not interact with catenins. The flamingo cadherins are located at the plasma membrane and have nine cadherin domains, seven epidermal growth factor-like repeats and two laminin A G-type repeats in their ectodomain. They also have seven transmembrane domains, a characteristic unique to this subfamily. It is postulated that these proteins are receptors involved in contact-mediated communication, with cadherin domains acting as homophilic binding regions and the EGF-like domains involved in cell adhesion and receptor-ligand interactions. The specific function of this particular member has not been determined.[6]
See also[edit]
References[edit]
- ^abcGRCh38: Ensembl release 89: ENSG00000008300–Ensembl,May 2017
- ^abcGRCm38: Ensembl release 89: ENSMUSG00000023473–Ensembl,May 2017
- ^"Human PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^"Mouse PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^Nakayama M, Nakajima D, Nagase T, Nomura N, Seki N, Ohara O (Sep 1998). "Identification of high-molecular-weight proteins with multiple EGF-like motifs by motif-trap screening".Genomics.51(1): 27–34.doi:10.1006/geno.1998.5341.PMID9693030.
- ^ab"Entrez Gene: CELSR3 cadherin, EGF LAG seven-pass G-type receptor 3 (flamingo homolog, Drosophila)".
Further reading[edit]
- Bonaldo MF, Lennon G, Soares MB (1997)."Normalization and subtraction: two approaches to facilitate gene discovery".Genome Res.6(9): 791–806.doi:10.1101/gr.6.9.791.PMID8889548.
- Wu Q, Maniatis T (1999)."A striking organization of a large family of human neural cadherin-like cell adhesion genes".Cell.97(6): 779–90.doi:10.1016/S0092-8674(00)80789-8.PMID10380929.S2CID6014717.
- Wu Q, Maniatis T (2000)."Large exons encoding multiple ectodomains are a characteristic feature of protocadherin genes".Proc. Natl. Acad. Sci. U.S.A.97(7): 3124–9.doi:10.1073/pnas.060027397.PMC16203.PMID10716726.
- Formstone CJ, Barclay J, Rees M, Little PF (2000). "Chromosomal localization of Celsr2 and Celsr3 in the mouse; Celsr3 is a candidate for the tippy (tip) lethal mutant on chromosome 9".Mamm. Genome.11(5): 392–4.doi:10.1007/s003350010073.PMID10790539.S2CID21333332.
- Nakayama M, Kikuno R, Ohara O (2003)."Protein–Protein Interactions Between Large Proteins: Two-Hybrid Screening Using a Functionally Classified Library Composed of Long cDNAs".Genome Res.12(11): 1773–84.doi:10.1101/gr.406902.PMC187542.PMID12421765.
- 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.Bibcode:2002PNAS...9916899M.doi:10.1073/pnas.242603899.PMC139241.PMID12477932.
- Bjarnadóttir TK, Fredriksson R, Höglund PJ, et al. (2005). "The human and mouse repertoire of the adhesion family of G-protein-coupled receptors".Genomics.84(1): 23–33.doi:10.1016/j.ygeno.2003.12.004.PMID15203201.
External links[edit]
- HumanCELSR3genome location andCELSR3gene details page in theUCSC Genome Browser.
This article incorporates text from theUnited States National Library of Medicine,which is in thepublic domain.