Homo sapiens Protein: RBM15
Summary
InnateDB Protein IDBP-100968.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RBM15
Protein Name RNA binding motif protein 15
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000358799
InnateDB Gene IDBG-100966 (RBM15)
Protein Structure
UniProt Annotation
Function May function as an mRNA export factor, stimulating export and expression of RTE-containing mRNAs which are present in many retrotransposons that require to be exported prior to splicing. High affinity binding of pre-mRNA to RBM15 may allow targeting of the mRNP to the export helicase DBP5 in a manner that is independent of splicing-mediated NXF1 deposition, resulting in export prior to splicing. May be implicated in HOX gene regulation. {ECO:0000269PubMed:17001072, ECO:0000269PubMed:19786495}.
Subcellular Localization Nucleus. Nucleus membrane; Peripheral membrane protein. Note=Colocalizes at the nuclear pore with DBP5 and NXF1.
Disease Associations Note=A chromosomal aberration involving RBM15 may be a cause of acute megakaryoblastic leukemia. Translocation t(1;22)(p13;q13) with MKL1. Although both reciprocal fusion transcripts are detected in acute megakaryoblastic leukemia (AMKL, FAB-M7), the RBM15-MKL1 chimeric protein has all the putative functional domains encoded by each gene and is the candidate oncogene.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 28 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 28 [view]
Protein-Protein 23 [view]
Protein-DNA 4 [view]
Protein-RNA 1 [view]
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0003676 nucleic acid binding
GO:0005515 protein binding
GO:0044822 poly(A) RNA binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001569 patterning of blood vessels
GO:0007221 positive regulation of transcription of Notch receptor target
GO:0016032 viral process
GO:0045638 negative regulation of myeloid cell differentiation
GO:0048536 spleen development
GO:0060412 ventricular septum morphogenesis
GO:0060674 placenta blood vessel development
Cellular Component
GO:0005634 nucleus
GO:0031965 nuclear membrane
Protein Structure and Domains
PDB ID
InterPro IPR000504 RNA recognition motif domain
IPR010912 Spen paralogue/orthologue C-terminal, metazoa
IPR012921 Spen paralogue and orthologue SPOC, C-terminal
IPR016194 SPOC like C-terminal domain
PFAM PF00076
PF07744
PRINTS
PIRSF
SMART SM00360
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q96T37
PhosphoSite PhosphoSite-Q96T37
TrEMBL
UniProt Splice Variant
Entrez Gene 64783
UniGene Hs.435947
RefSeq
HUGO HGNC:14959
OMIM 606077
CCDS CCDS822
HPRD 05832
IMGT
EMBL AF364035 AF368062 AF368063 AF368064 AJ297259 AJ303089 AJ303090 AK022541 AK025596 AL355488 BC006397 BC047479 BC062316 BC098140 BC103493 BC103507 BK005915 CH471122
GenPept AAH06397 AAH47479 AAH62316 AAH98140 AAI03494 AAI03508 AAK54722 AAK54723 AAK54724 AAK56920 BAB14088 BAB15185 CAC38828 CAC38829 CAC38861 CAC38862 CAI19077 DAA05818 EAW56439