FXR2
Sign in to saveAlso known as FMR1L2, FXR2P, FMR1 autosomal homolog 2
Fragile X mental retardation syndrome-related protein 2 is a protein that in humans is encoded by the FXR2 gene.
In the Vinony graph
Vinony's link graph records 14 inbound references to FXR2, and connects out to PubMed, human chromosome 17 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 17.
Vinony links it to 5 Wikipedia language editions.
Gene data
FXR2- Name
- FMR1 autosomal homolog 2
- Type
- protein-coding
- Position
- 7,591,230–7,614,916 (−)
- Aliases
- FMR1L2, FXR2P
- Ensembl
- ENSG00000129245
- RefSeq RNA
- NM_004860.4, XM_047437106.1, XM_054317873.1
- RefSeq protein
- NP_004851.2, XP_047293062.1, XP_054173848.1
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 cognitive disability syndrome. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
via MyGene.info
Gene · Ensembl
FMR1 autosomal homolog 2
- Symbol
- FXR2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 17:7,591,230-7,614,916
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 21014
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/9513
- genomic end
- 7614897
- genomic start
- 7494548
- chromosome
- human chromosome 17
- cytogenetic location
- 17p13.1
- expressed in
- ventral tegmental area
Sources (3)
via Wikidata · CC0
~1 min read
Encyclopedic overview
4 sectionsContents
- Function
- Interactions
- References
- Further reading
Fragile X mental retardation syndrome-related protein 2 is a protein that in humans is encoded by the FXR2 gene.
== Function ==
Excerpted from Wikipedia’s “FXR2” article, available under the CC BY-SA 4.0 licence.