FXR1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Fragile X mental retardation syndrome-related protein 1 is a protein that in humans is encoded by the FXR1 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesFXR1, FXR1P, FMR1 autosomal homolog 1, MYORIBF, MYOPMIL
Quick facts Available structures, PDB ...
FXR1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesFXR1, FXR1P, FMR1 autosomal homolog 1, MYORIBF, MYOPMIL
External IDsOMIM: 600819; MGI: 104860; HomoloGene: 3573; GeneCards: FXR1; OMA:FXR1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001013438
NM_001013439
NM_005087
NM_001363882

NM_001113188
NM_001113189
NM_008053

RefSeq (protein)

NP_001013456
NP_001013457
NP_005078
NP_001350811

NP_001106659
NP_001106660
NP_032079

Location (UCSC)Chr 3: 180.87 – 180.98 MbChr 3: 34.07 – 34.12 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene is an RNA binding protein that interacts with the functionally similar proteins FMR1 and FXR2. These proteins shuttle between the nucleus and cytoplasm and associate with polyribosomes, predominantly with the 60S ribosomal subunit. Three transcript variants encoding different isoforms have been found for this gene.[7]

Interactions

FXR1 has been shown to interact with FXR2,[8][9] FMR1[8][9] and CYFIP2.[10]

References

Further reading

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