RBM9

RBFOX2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRBFOX2, FOX2, Fox-2, HNRBP2, HRNBP2, RBM9, RTA, dJ106I20.3, fxh, RNA binding protein, fox-1 homolog 2
External IDsMGI: 1933973 HomoloGene: 49375 GeneCards: RBFOX2
Gene location (Human)
Chr.Chromosome 22 (human)[1]
BandNo data availableStart35,738,736 bp[1]
End36,028,425 bp[1]
RNA expression pattern


More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

23543

93686

Ensembl

ENSG00000277564
ENSG00000100320

ENSMUSG00000033565

UniProt

O43251

Q8BP71

RefSeq (mRNA)
RefSeq (protein)
Location (UCSC)Chr 22: 35.74 – 36.03 MbChr 22: 77.08 – 77.31 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

RNA binding motif protein 9, also known as RBM9 or FOX-2, is a protein which in humans is encoded by the RBM9 gene.[5]

Function

RBM9 is one of several human genes similar to the C. elegans gene Fox-1. This gene encodes an RNA binding protein that is thought to be a key regulator of alternative exon splicing in the nervous system and other cell types. The protein binds to a conserved UGCAUG element found downstream of many alternatively spliced exons and promotes inclusion of the alternative exon in mature transcripts. The protein also interacts with the estrogen receptor 1 transcription factor and regulates estrogen receptor 1 transcriptional activity. Multiple transcript variants encoding different isoforms have been found for this gene.[5]

RBM9, as determined by CLIP-seq, binds near alternatively spliced exons and regulates the inclusion or exclusion of exons during alternative splicing by binding in introns either downstream (inclusion) or upstream (exon skipping) of exons. Its presence is important for stem cell survival and knockdowns of RBM9 activate markers for apoptosis.[6]

References

Further reading


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