Homo sapiens Protein: FXR1
Summary
InnateDB Protein IDBP-66613.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FXR1
Protein Name fragile X mental retardation, autosomal homolog 1
Synonyms FXR1P;
Species Homo sapiens
Ensembl Protein ENSP00000350170
InnateDB Gene IDBG-66609 (FXR1)
Protein Structure
UniProt Annotation
Function RNA-binding protein required for embryonic and postnatal development of muscle tissue. May regulate intracellular transport and local translation of certain mRNAs (By similarity). {ECO:0000250}.
Subcellular Localization Cytoplasm {ECO:0000269PubMed:7781595}.
Disease Associations
Tissue Specificity Expressed in all tissues examined including heart, brain, kidney and testis. {ECO:0000269PubMed:7781595}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 45 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Experimentally validated
Total 45 [view]
Protein-Protein 42 [view]
Protein-DNA 2 [view]
Protein-RNA 1 [view]
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0002151 G-quadruplex RNA binding
GO:0003723 RNA binding
GO:0003730 mRNA 3'-UTR binding
GO:0005515 protein binding
GO:0044822 poly(A) RNA binding
Biological Process
GO:0006915 apoptotic process
GO:0007517 muscle organ development
GO:0017148 negative regulation of translation
GO:0030154 cell differentiation
GO:0045087 innate immune response (InnateDB)
Cellular Component
GO:0005634 nucleus
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0005844 polysome
GO:0016020 membrane
GO:0043034 costamere
Protein Structure and Domains
PDB ID
InterPro IPR004087 K Homology domain
IPR004088 K Homology domain, type 1
IPR008395 Agenet-like domain
IPR012340 Nucleic acid-binding, OB-fold
IPR022034 Fragile X mental retardation protein family
PFAM PF00013
PF13014
PF05641
PF12235
PRINTS
PIRSF
SMART SM00322
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P51114
PhosphoSite PhosphoSite-P51114
TrEMBL C9JZE0
UniProt Splice Variant
Entrez Gene 8087
UniGene Hs.478407
RefSeq NP_005078
HUGO HGNC:4023
OMIM 600819
CCDS CCDS3238
HPRD 02892
IMGT
EMBL AC008009 AC068638 AC108734 AK292633 AY341428 BC028983 U25165
GenPept AAC50155 AAH28983 AAQ20045 BAF85322