RBM11

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]
End	14,228,372 bp[1]
Gene location (Mouse)
Chr.	Chromosome 16 (mouse)[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
	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

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

References

GRCh38: Ensembl release 89: ENSG00000185272 - Ensembl, May 2017
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.
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.
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.

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