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Gene : CRABP2 Homo sapiens

Name  ? cellular retinoic acid binding protein 2 Cytological Location  1q23.1
Brief Description  cellular retinoic acid binding protein 2
Description  This gene encodes a member of the retinoic acid (RA, a form of vitamin A) binding protein family and lipocalin/cytosolic fatty-acid binding protein family. The protein is a cytosol-to-nuclear shuttling protein, which facilitates RA binding to its cognate receptor complex and transfer to the nucleus. It is involved in the retinoid signaling pathway, and is associated with increased circulating low-density lipoprotein cholesterol. Alternatively spliced transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2010]
  • synonyms:
  • OTTHUMG00000041300,
  • CRABP-II,
  • RBP6,
  • NM_001878,
  • uc021pbi.2,
  • CRABP-II,
  • cellular retinoic acid-binding protein 2,
  • HGNC:2339,
  • CRABP2,
  • BC001109
  • identifiers:
  • 1382,
  • ENSG00000143320,
  • CRABP2

Genome feature

Region: gene ? Length: 6211  
Location: 1:156699606-156705816 reverse strand Cyto location: 1q23.1


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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

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]

Homology

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Interactions

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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

138 SN Ps

5 Cross References

16 Data Sets

10 Homologues

0 Located Features

97 Rna Seq Results