RCAN3
RCAN3 is a gene that in humans encodes the Calcipressin-3 protein.
Calcipressin-3 is a protein that in humans is encoded by the RCAN3 gene.[1][2]
Summary box
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See also
References
- ↑ Strippoli P, Lenzi L, Petrini M, Carinci P, Zannotti M (May 2000). “A new gene family including DSCR1 (Down Syndrome Candidate Region 1) and ZAKI-4: characterization from yeast to human and identification of DSCR1-like 2, a novel human member (DSCR1L2)”. Genomics. 64 (3): 252–63. doi:10.1006/geno.2000.6127. PMID 10756093.
- ↑ “Entrez Gene: DSCR1L2 Down syndrome critical region gene 1-like 2”.
Further reading
- Facchin F, Canaider S, Vitale L, et al. (2008). “Identification and analysis of human RCAN3 (DSCR1L2) mRNA and protein isoforms”. Gene. 407 (1–2): 159–68. doi:10.1016/j.gene.2007.10.006. PMID 18022329.
- Mulero MC, Aubareda A, Schlüter A, Pérez-Riba M (2007). “RCAN3, a novel calcineurin inhibitor that down-regulates NFAT-dependent cytokine gene expression”. Biochim. Biophys. Acta. 1773 (3): 330–41. doi:10.1016/j.bbamcr.2006.12.007. PMID 17270291.
- Olsen JV, Blagoev B, Gnad F, et al. (2006). “Global, in vivo, and site-specific phosphorylation dynamics in signaling networks”. Cell. 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983.
- 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:10.1038/nature04727. PMID 16710414.
- Canaider S, Facchin F, Griffoni C, et al. (2006). “Proteins encoded by human Down syndrome critical region gene 1-like 2 (DSCR1L2) mRNA and by a novel DSCR1L2 mRNA isoform interact with cardiac troponin I (TNNI3)”. Gene. 372: 128–36. doi:10.1016/j.gene.2005.12.029. PMID 16516408.
- 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. PMC 528928. PMID 15489334.
- 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. PMC 139241. PMID 12477932.
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