RBM11

RBM11
Identifiers
Aliases	RBM11, RNA binding motif protein 11
External IDs	OMIM: 617937; MGI: 2447622; HomoloGene: 16988; GeneCards: RBM11; OMA:RBM11 - orthologs
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	2YWK
Gene location (Human)
Chr.	Chromosome 21 (human)
End	14,228,372 bp
Gene location (Mouse)
Chr.	Chromosome 16 (mouse)
End	75,399,717 bp
RNA expression pattern
	Top expressed in
	corpus epididymis; ; C1 segment; ; testicle; ; gonad; ; oocyte; ; tibial nerve; ; left ovary; ; Brodmann area 9; ; prefrontal cortex; ; secondary oocyte;
	Top expressed in
	lumbar spinal ganglion; ; spermatocyte; ; embryo; ; dentate gyrus of hippocampal formation granule cell; ; embryo; ; facial motor nucleus; ; seminiferous tubule; ; primary visual cortex; ; ganglion of neuraxis; ; superior frontal gyrus;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	nucleic acid binding; protein binding; protein homodimerization activity; RNA binding; poly(U) RNA binding; single-stranded RNA binding;
Cellular component	nuclear speck; 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
	54033
	224344
	ENSG00000185272
	ENSMUSG00000032940
	P57052
	Q80YT9
	NM_144770; NM_001320602
	NM_198302
	NP_001307531; NP_658983
	NP_938044
	Wikidata
View/Edit Human	View/Edit Mouse

Splicing regulator RBM11 is a protein that is encoded by the RBM11 gene^[5]^[6] in humans.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000185272 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000032940 – Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ 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.
↑ "Entrez Gene: RBM11 RNA binding motif protein 11".

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. Bibcode:2002PNAS...9916899M. 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.

This article on a gene on human chromosome 21 is a stub. You can help Wikipedia by adding missing information.

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000185272 – Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 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.

[pmid12036298-5] 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.

[entrez-6] "Entrez Gene: RBM11 RNA binding motif protein 11".

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RBM11

References

Further reading