RWDD2B: Difference between revisions
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'''RWD domain-containing protein 2B''' is a [[protein]] that in humans is encoded by the ''RWDD2B'' [[gene]].<ref name="pmid10729227">{{cite journal | vauthors = Orti R, Rachidi M, Vialard F, Toyama K, Lopes C, Taudien S, Rosenthal A, Yaspo ML, Sinet PM, Delabar JM | title = Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5 | journal = Genomics | volume = 64 | issue = 2 | pages = 203–10 |date=May 2000 | pmid = 10729227 | pmc = | doi = 10.1006/geno.1999.6109 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: C21orf6 chromosome 21 open reading frame 6| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10069| accessdate = }}</ref> | '''RWD domain-containing protein 2B''' is a [[protein]] that in humans is encoded by the ''RWDD2B'' [[gene]].<ref name="pmid10729227">{{cite journal | vauthors = Orti R, Rachidi M, Vialard F, Toyama K, Lopes C, Taudien S, Rosenthal A, Yaspo ML, Sinet PM, Delabar JM | title = Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5 | journal = Genomics | volume = 64 | issue = 2 | pages = 203–10 |date=May 2000 | pmid = 10729227 | pmc = | doi = 10.1006/geno.1999.6109 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: C21orf6 chromosome 21 open reading frame 6| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10069| accessdate = }}</ref> | ||
Revision as of 19:22, 19 February 2018
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RWD domain-containing protein 2B is a protein that in humans is encoded by the RWDD2B gene.[1][2]
References
- ↑ Orti R, Rachidi M, Vialard F, Toyama K, Lopes C, Taudien S, Rosenthal A, Yaspo ML, Sinet PM, Delabar JM (May 2000). "Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5". Genomics. 64 (2): 203–10. doi:10.1006/geno.1999.6109. PMID 10729227.
- ↑ "Entrez Gene: C21orf6 chromosome 21 open reading frame 6".
Further reading
- Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
- 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.
- 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.
- 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.
- Hattori M, Fujiyama A, Taylor TD, et al. (2000). "The DNA sequence of human chromosome 21". Nature. 405 (6784): 311–9. doi:10.1038/35012518. PMID 10830953.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
External links
- RWDD2B human gene location in the UCSC Genome Browser.
- RWDD2B human gene details in the UCSC Genome Browser.
 | This article on a gene on human chromosome 21 is a stub. You can help Wikipedia by expanding it. |