Homo sapiens Gene: RBP7
Summary
InnateDB Gene IDBG-88824.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RBP7
Gene Name retinol binding protein 7, cellular
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000162444
Encoded Proteins
retinol binding protein 7, cellular
retinol binding protein 7, cellular
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Due to its chemical instability and low solubility in aqueous solution, vitamin A requires cellular retinol-binding proteins (CRBPs), such as RBP7, for stability, internalization, intercellular transfer, homeostasis, and metabolism.[supplied by OMIM, May 2004]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:9997206-10016020
Strand Forward strand
Band p36.22
Transcripts
ENST00000294435 ENSP00000294435
ENST00000315901 ENSP00000324228
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005215 transporter activity
GO:0005501 retinoid binding
GO:0008289 lipid binding
GO:0016918 retinal binding
GO:0019841 retinol binding
Biological Process
GO:0006810 transport
Cellular Component
GO:0005737 cytoplasm
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL B1AQ60
UniProt Splice Variant
Entrez Gene 116362
UniGene
RefSeq NM_052960
HUGO HGNC:30316
OMIM 608604
CCDS CCDS109
HPRD 16355
IMGT
EMBL AL590639 AL603962 CH471130
GenPept EAW71637
RNA Seq Atlas 116362