FXR2

FXR2
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	3H8Z
Identifiers
Aliases	FXR2, FMR1L2, FXR2P, FMR1 autosomal homolog 2
External IDs	OMIM: 605339; MGI: 1346074; HomoloGene: 21014; GeneCards: FXR2; OMA:FXR2 - orthologs
Gene location (Human)
Chr.	Chromosome 17 (human)
End	7,614,897 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	69,544,123 bp
RNA expression pattern
	Top expressed in
	apex of heart; ; gastrocnemius muscle; ; muscle of thigh; ; superior vestibular nucleus; ; left ventricle; ; Pons; ; right hemisphere of cerebellum; ; inferior ganglion of vagus nerve; ; right auricle of heart; ; ventral tegmental area;
	Top expressed in
	neural layer of retina; ; dentate gyrus of hippocampal formation granule cell; ; muscle of thigh; ; superior frontal gyrus; ; primary visual cortex; ; ventricular zone; ; cerebellar cortex; ; epiblast; ; spermatocyte; ; lip;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	protein heterodimerization activity; nucleic acid binding; protein binding; mRNA binding; protein homodimerization activity; identical protein binding; RNA binding; mRNA 3'-UTR binding; translation regulator activity;
Cellular component	polysome; cytosolic large ribosomal subunit; extracellular exosome; membrane; nucleus; cytoplasm; cytosol; postsynaptic density; axon; ribonucleoprotein granule; cytoplasmic ribonucleoprotein granule; soma; dendritic spine;
Biological process	negative regulation of translation; regulation of translation; regulation of mRNA stability; positive regulation of translation;
	Sources:Amigo / QuickGO
Orthologs
	9513
	23879
	ENSG00000129245
	ENSMUSG00000018765
	P51116
	Q9WVR4; Q6P5B5
	NM_004860
	NM_011814
	NP_004851
	NP_035944
	Wikidata
View/Edit Human	View/Edit Mouse

Fragile X mental retardation syndrome-related protein 2 is a protein that in humans is encoded by the FXR2 gene.