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Gene : RARA Homo sapiens

Name  ? retinoic acid receptor alpha Cytological Location  17q21.2
Brief Description  retinoic acid receptor alpha
description  This gene represents a nuclear retinoic acid receptor. The encoded protein, retinoic acid receptor alpha, regulates transcription in a ligand-dependent manner. This gene has been implicated in regulation of development, differentiation, apoptosis, granulopoeisis, and transcription of clock genes. Translocations between this locus and several other loci have been associated with acute promyelocytic leukemia. Alternatively spliced transcript variants have been found for this locus.[provided by RefSeq, Sep 2010]
  • synonyms:
  • OTTHUMG00000133328,
  • uc002huk.3,
  • retinoic acid receptor, alpha,
  • X06538,
  • NM_000964,
  • RAR,
  • HGNC:9864,
  • NR1B1,
  • RAR,
  • RARA,
  • NR1B1
  • identifiers:
  • 5914,
  • ENSG00000131759,
  • RARA

Genome feature

Region: gene ? Length: 48464  
Location: 17:40309180-40357643 Cyto location: 17q21.2

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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


1 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 --> Orthologues


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



54 SN Ps

5 Cross References

18 Data Sets

22 Homologues

0 Located Features

97 Rna Seq Results