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Gene : FXR1 Homo sapiens

Name  ? FMR1 autosomal homolog 1 Cytological Location  3q26.33
Brief Description  FMR1 autosomal homolog 1
Description  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. [provided by RefSeq, Jul 2008]
  • synonyms:
  • MYOPMIL,
  • fragile X mental retardation, autosomal homolog 1,
  • uc003fkq.4,
  • HGNC:4023,
  • FXR1P,
  • FXR1,
  • NM_001013438,
  • OTTHUMG00000158138,
  • M67468,
  • MYORIBF
  • identifiers:
  • 8087,
  • ENSG00000114416,
  • FXR1

Genome feature

Region: gene ? Length: 70084  
Location: 3:180912670-180982753 Cyto location: 3q26.33


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

2 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

354 SN Ps

5 Cross References

18 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results