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Gene : FXR2 Homo sapiens

Name  ? FMR1 autosomal homolog 2 Cytological Location  17p13.1
Brief Description  FMR1 autosomal homolog 2
Description  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]
  • synonyms:
  • OTTHUMG00000178237,
  • U31501,
  • FMR1L2,
  • uc002gia.3,
  • FMR1L2,
  • FXR2P,
  • NM_004860,
  • fragile X mental retardation, autosomal homolog 2,
  • HGNC:4024,
  • FXR2
  • identifiers:
  • 9513,
  • ENSG00000129245,
  • FXR2

Genome feature

Region: gene ? Length: 23668  
Location: 17:7591230-7614897 reverse strand Cyto location: 17p13.1

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

83 SN Ps

5 Cross References

17 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results