RBM11

Putative RNA-binding protein 11 is a protein that in humans is encoded by the RBM11 gene.[5][6]

RBM11
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2YWK
Identifiers
Aliases	RBM11, RNA binding motif protein 11
External IDs	OMIM: 617937 MGI: 2447622 HomoloGene: 16988 GeneCards: RBM11
Gene location (Human) Chr. Chromosome 21 (human)[1] Band 21q11.2 Start 14,216,130 bp[1] End 14,228,372 bp[1]
Gene location (Mouse) Chr. Chromosome 16 (mouse)[2] Band 16|16 C3.1 Start 75,592,844 bp[2] End 75,602,829 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • nucleic acid binding • GO:0001948 protein binding • protein homodimerization activity • RNA binding • poly(U) RNA binding • single-stranded RNA binding Cellular component • nuclear speck • cell nucleus • nucleoplasm Biological process • multicellular organism development • cellular response to oxidative stress • mRNA processing • cell differentiation • regulation of alternative mRNA splicing, via spliceosome • RNA splicing Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	54033	224344
Ensembl	ENSG00000185272	ENSMUSG00000032940
UniProt	P57052	Q80YT9
RefSeq (mRNA)	NM_144770 NM_001320602	NM_198302
RefSeq (protein)	NP_001307531 NP_658983	NP_938044
Location (UCSC)	Chr 21: 14.22 – 14.23 Mb	Chr 16: 75.59 – 75.6 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. GRCh38: Ensembl release 89: ENSG00000185272 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000032940 - 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. Gardiner K, Slavov D, Bechtel L, Davisson M (May 2002). "Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis". Genomics. 79 (6): 833–43. doi:10.1006/geno.2002.6782. PMID 12036298.
6. "Entrez Gene: RBM11 RNA binding motif protein 11".

Further reading

• Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration". Cell. 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569. S2CID 13709685.
• 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. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.
• 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. Bibcode:2000Natur.405..311H. doi:10.1038/35012518. PMID 10830953.
• Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.