RBM11

RBM11

Available structures

Ortholog search: PDBe RCSB

List of PDB id codes
2YWK

Identifiers

External IDs

MGI: 2447622 HomoloGene: 16988 GeneCards: RBM11

Gene ontology
Molecular function	• nucleic acid binding • nucleotide binding • protein binding • protein homodimerization activity • RNA binding • poly(U) 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

RNA expression pattern

More reference expression data

Orthologs

Species

Human

Mouse


54033


224344


ENSG00000185272


ENSMUSG00000032940


P57052


Q80YT9

RefSeq (mRNA)


NM_144770 NM_001320602


NM_198302

RefSeq (protein)


NP_658983.3 NP_001307531.1


NP_938044.1

Location (UCSC)

Chr 21: 14.22 – 14.23 Mb

Chr 16: 75.59 – 75.6 Mb

PubMed search

^[1]

^[2]

View/Edit Human

View/Edit Mouse

Putative RNA-binding protein 11 is a protein that in humans is encoded by the RBM11 gene.^[3]^[4]

References

↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ 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".

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.
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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