Bos taurus Gene: RBM10
Summary
InnateDB Gene IDBG-636494.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RBM10
Gene Name RNA-binding protein 10
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000002890
Encoded Proteins
RNA binding motif protein 10
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000182872:
This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome X:90794365-90820965
Strand Forward strand
Band
Transcripts
ENSBTAT00000003758 ENSBTAP00000003758
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 38 interaction(s) predicted by orthology.
Predicted by orthology
Total 38 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0003676 nucleic acid binding
GO:0005515 protein binding
GO:0032403 protein complex binding
GO:0042802 identical protein binding
GO:0044822 poly(A) RNA binding
GO:0046872 metal ion binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0008285 negative regulation of cell proliferation
GO:0034391 regulation of smooth muscle cell apoptotic process
GO:0034393 positive regulation of smooth muscle cell apoptotic process
GO:0070935 3'-UTR-mediated mRNA stabilization
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL F1MFZ9
UniProt Splice Variant
Entrez Gene 505749
UniGene
RefSeq
HUGO HGNC:9896
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02073009 DAAA02073010 DAAA02073011 DAAA02073012 DAAA02073013 DAAA02073014
GenPept
RNA Seq Atlas 505749