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Gene information for FXR2 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID9513
Official gene symbolFXR2
Full namefragile X mental retardation, autosomal homolog 2
Aliases,FMR1L2,
Gene summaryThe 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]
LocationChromosome: 17   Locus: 17p13.1
Gene position7518215 - 7494548  Map Viewer
Gene orientationminus
Gene size23668 bp
Gene sequence
OMIM ID605339