SNX27
From Wikipedia, the free encyclopedia
Sorting nexin family member 27
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Identifiers | |||||||||||
Symbol(s) | SNX27; KIAA0488; MGC126871; MGC126873; MGC20471; MY014 | ||||||||||
External IDs | MGI: 1923992 HomoloGene: 12797 | ||||||||||
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RNA expression pattern | |||||||||||
Orthologs | |||||||||||
Human | Mouse | ||||||||||
Entrez | 81609 | 76742 | |||||||||
Ensembl | ENSG00000143376 | ENSMUSG00000028136 | |||||||||
Uniprot | Q96L92 | n/a | |||||||||
Refseq | NM_030918 (mRNA) NP_112180 (protein) |
XM_131051 (mRNA) XP_131051 (protein) |
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Location | Chr 1: 149.85 - 149.94 Mb | Chr 3: 94.58 - 94.67 Mb | |||||||||
Pubmed search | [1] | [2] |
Sorting nexin family member 27, also known as SNX27, is a human gene.[1]
This gene encodes a member of the sorting nexin family, a diverse group of cytoplasmic and membrane-associated proteins involved in endocytosis of plasma membrane receptors and protein trafficking through these compartments. All members of this protein family contain a phosphoinositide binding domain (PX domain). A highly similar protein in mouse is responsible for the specific recruitment of an isoform of serotonin 5-hydroxytryptamine 4 receptor into early endosomes, suggesting the analogous role for the human protein.[1]
[edit] References
[edit] Further reading
- Worby CA, Dixon JE (2003). "Sorting out the cellular functions of sorting nexins.". Nat. Rev. Mol. Cell Biol. 3 (12): 919–31. doi: . PMID 12461558.
- Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery.". Genome Res. 6 (9): 791–806. PMID 8889548.
- Seki N, Ohira M, Nagase T, et al. (1998). "Characterization of cDNA clones in size-fractionated cDNA libraries from human brain.". DNA Res. 4 (5): 345–9. PMID 9455484.
- Teasdale RD, Loci D, Houghton F, et al. (2001). "A large family of endosome-localized proteins related to sorting nexin 1.". Biochem. J. 358 (Pt 1): 7–16. PMID 11485546.
- 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: . PMID 12477932.
- 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: . PMID 14702039.
- Williams R, Schlüter T, Roberts MS, et al. (2005). "Sorting nexin 17 accelerates internalization yet retards degradation of P-selectin.". Mol. Biol. Cell 15 (7): 3095–105. doi: . PMID 15121882.
- Joubert L, Hanson B, Barthet G, et al. (2005). "New sorting nexin (SNX27) and NHERF specifically interact with the 5-HT4a receptor splice variant: roles in receptor targeting.". J. Cell. Sci. 117 (Pt 22): 5367–79. doi: . PMID 15466885.
- Gregory SG, Barlow KF, McLay KE, et al. (2006). "The DNA sequence and biological annotation of human chromosome 1.". Nature 441 (7091): 315–21. doi: . PMID 16710414.
- Rincón E, Santos T, Avila-Flores A, et al. (2007). "Proteomics identification of sorting nexin 27 as a diacylglycerol kinase zeta-associated protein: new diacylglycerol kinase roles in endocytic recycling.". Mol. Cell Proteomics 6 (6): 1073–87. doi: . PMID 17351151.
- MacNeil AJ, Mansour M, Pohajdak B (2007). "Sorting nexin 27 interacts with the Cytohesin associated scaffolding protein (CASP) in lymphocytes.". Biochem. Biophys. Res. Commun. 359 (4): 848–53. doi: . PMID 17577583.