RPH3AL

Revision as of 14:17, 6 September 2012 by WikiBot (talk | contribs) (Robot: Automated text replacement (-{{reflist}} +{{reflist|2}}, -<references /> +{{reflist|2}}, -{{WikiDoc Cardiology Network Infobox}} +))
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search


Rabphilin 3A-like (without C2 domains)
Identifiers
Symbols RPH3AL ; NOC2
External IDs Template:OMIM5 Template:MGI HomoloGene5078
RNA expression pattern
File:PBB GE RPH3AL 221614 s 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

Rabphilin 3A-like (without C2 domains), also known as RPH3AL, is a human gene.[1]


References

  1. "Entrez Gene: RPH3AL rabphilin 3A-like (without C2 domains)".

Further reading

  • Kotake K, Ozaki N, Mizuta M; et al. (1997). "Noc2, a putative zinc finger protein involved in exocytosis in endocrine cells". J. Biol. Chem. 272 (47): 29407–10. PMID 9367993.
  • Smith JS, Tachibana I, Allen C; et al. (1999). "Cloning of a human ortholog (RPH3AL) of (RNO)Rph3al from a candidate 17p13.3 medulloblastoma tumor suppressor locus". Genomics. 59 (1): 97–101. doi:10.1006/geno.1999.5864. PMID 10395805.
  • Fenster SD, Chung WJ, Zhai R; et al. (2000). "Piccolo, a presynaptic zinc finger protein structurally related to bassoon". Neuron. 25 (1): 203–14. PMID 10707984.
  • Haynes LP, Evans GJ, Morgan A, Burgoyne RD (2001). "A direct inhibitory role for the Rab3-specific effector, Noc2, in Ca2+-regulated exocytosis in neuroendocrine cells". J. Biol. Chem. 276 (13): 9726–32. doi:10.1074/jbc.M006959200. PMID 11134008.
  • Goi T, Takeuchi K, Katayama K; et al. (2003). "Mutations of rabphillin-3A-like gene in colorectal cancers". Oncol. Rep. 9 (6): 1189–92. PMID 12375017.
  • Milkereit P, Strauss D, Bassler J; et al. (2003). "A Noc complex specifically involved in the formation and nuclear export of ribosomal 40 S subunits". J. Biol. Chem. 278 (6): 4072–81. doi:10.1074/jbc.M208898200. PMID 12446671.
  • 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.
  • Fukuda M (2003). "Distinct Rab binding specificity of Rim1, Rim2, rabphilin, and Noc2. Identification of a critical determinant of Rab3A/Rab27A recognition by Rim2". J. Biol. Chem. 278 (17): 15373–80. doi:10.1074/jbc.M212341200. PMID 12578829.
  • Cardoso C, Leventer RJ, Ward HL; et al. (2003). "Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3". Am. J. Hum. Genet. 72 (4): 918–30. PMID 12621583.
  • Cheviet S, Coppola T, Haynes LP; et al. (2004). "The Rab-binding protein Noc2 is associated with insulin-containing secretory granules and is essential for pancreatic beta-cell exocytosis". Mol. Endocrinol. 18 (1): 117–26. doi:10.1210/me.2003-0300. PMID 14593078.
  • 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.
  • Manabe S, Nishimura N, Yamamoto Y; et al. (2004). "Identification and characterization of Noc2 as a potential Rab3B effector protein in epithelial cells". Biochem. Biophys. Res. Commun. 316 (1): 218–25. doi:10.1016/j.bbrc.2004.02.026. PMID 15003533.
  • Matsumoto M, Miki T, Shibasaki T; et al. (2004). "Noc2 is essential in normal regulation of exocytosis in endocrine and exocrine cells". Proc. Natl. Acad. Sci. U.S.A. 101 (22): 8313–8. doi:10.1073/pnas.0306709101. PMID 15159548.
  • 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.

Template:WikiDoc Sources