| Entrez gene ID | | 9513 |
| Official gene symbol | | FXR2 |
| Full name | | fragile X mental retardation, autosomal homolog 2 |
| Aliases | | ,FMR1L2, |
| 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] |
| Location | | Chromosome: 17 Locus: 17p13.1 |
| Gene position | | 7518215 - 7494548 Map Viewer |
| Gene orientation | | minus |
| Gene size | | 23668 bp |
| Gene sequence |
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| OMIM ID | | 605339 |