FXR2

GENE INFORMATION

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Gene name

FXR2 (HGNC Symbol)

Synonyms

FMR1L2

Description

fragile X mental retardation, autosomal homolog 2 (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is a RNA binding protein containing two KH domains and one RCG box, which is similar to FMRP and FXR1. It associates with polyribosomes, predominantly with 60S large ribosomal subunits. This encoded protein may self-associate or interact with FMRP and FXR1. It may have a role in the development of fragile X mental retardation syndrome. [provided by RefSeq, Jul 2008]

Chromosome

17 (Chromosome progress)

Cytoband

p13.1

Chromosome location (bp)

7494548 - 7518189

Ensembl

ENSG00000129245 (version 73.37)

Entrez gene

9513

UniProt

P51116 (UniProt - Evidence at protein level)

neXtProt

NX_P51116

Antibodypedia

FXR2 antibodies
 

PROTEIN VIEW

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FXR2-001
 
FXR2-002
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

FXR2-001 ENSP00000250113
ENST00000250113
P51116
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Show » 673 74.2 No 0
FXR2-002 ENSP00000459230
ENST00000571597
I3L1Z2
Show all »
118 13.7 No 0