RWDD2B

RWD domain-containing protein 2B is a protein that in humans is encoded by the RWDD2B gene.[5][6]

RWDD2B
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2DAX
Identifiers
Aliases	RWDD2B, C21orf6, GL011, RWD domain containing 2B
External IDs	OMIM: 617843 MGI: 1858215 HomoloGene: 9654 GeneCards: RWDD2B
Gene location (Human) Chr. Chromosome 21 (human)[1] Band 21q21.3 Start 29,004,384 bp[1] End 29,019,360 bp[1]
Gene location (Mouse) Chr. Chromosome 16 (mouse)[2] Band 16|16 C3.3 Start 87,433,407 bp[2] End 87,440,573 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • GO:0001948 protein binding • molecular function Cellular component • cellular component Biological process • biological process Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	10069	53858
Ensembl	ENSG00000156253	ENSMUSG00000041079
UniProt	P57060	Q99M03
RefSeq (mRNA)	NM_016940 NM_001320724	NM_016924
RefSeq (protein)	NP_001307653 NP_058636	NP_058620
Location (UCSC)	Chr 21: 29 – 29.02 Mb	Chr 16: 87.43 – 87.44 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. GRCh38: Ensembl release 89: ENSG00000156253 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000041079 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. 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.
6. "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.