Homo sapiens Protein: RARB | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-368081.5 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | RARB | ||||||||||||||||||||||
Protein Name | retinoic acid receptor, beta | ||||||||||||||||||||||
Synonyms | HAP; MCOPS12; NR1B2; RRB2; | ||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000391391 | ||||||||||||||||||||||
InnateDB Gene | IDBG-22486 (RARB) | ||||||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||||||
Function | Receptor for retinoic acid. Retinoic acid receptors bind as heterodimers to their target response elements in response to their ligands, all-trans or 9-cis retinoic acid, and regulate gene expression in various biological processes. The RXR/RAR heterodimers bind to the retinoic acid response elements (RARE) composed of tandem 5'-AGGTCA-3' sites known as DR1-DR5. In the absence or presence of hormone ligand, acts mainly as an activator of gene expression due to weak binding to corepressors. In concert with RARG, required for skeletal growth, matrix homeostasis and growth plate function. {ECO:0000269PubMed:12554770}. | ||||||||||||||||||||||
Subcellular Localization | Isoform Beta-1: Nucleus.Isoform Beta-2: Nucleus.Isoform Beta-4: Cytoplasm. | ||||||||||||||||||||||
Disease Associations | Microphthalmia, syndromic, 12 (MCOPS12) [MIM:615524]: A form of microphthalmia, a disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. MCOPS12 patients manifest variable features, including diaphragmatic hernia, pulmonary hypoplasia, and cardiac abnormalities. {ECO:0000269PubMed:24075189}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||
Tissue Specificity | |||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 37 experimentally validated interaction(s) in this database.
They are also associated with 8 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||
InterPro |
IPR000003
Retinoid X receptor/HNF4 IPR000536 Nuclear hormone receptor, ligand-binding, core IPR001628 Zinc finger, nuclear hormone receptor-type IPR001723 Steroid hormone receptor IPR001728 Thyroid hormone receptor IPR003070 Orphan nuclear receptor IPR003078 Retinoic acid receptor IPR008946 Nuclear hormone receptor, ligand-binding |
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PFAM |
PF00104
PF00105 |
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PRINTS |
PR00545
PR00047 PR00398 PR00546 PR01284 PR01292 |
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PIRSF | |||||||||||||||||||||||
SMART |
SM00430
SM00399 |
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TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | P10826 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-P10826 | ||||||||||||||||||||||
TrEMBL | Q5QHG3 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 5915 | ||||||||||||||||||||||
UniGene | Hs.735252 | ||||||||||||||||||||||
RefSeq | NP_001277146 | ||||||||||||||||||||||
HUGO | HGNC:9865 | ||||||||||||||||||||||
OMIM | 180220 | ||||||||||||||||||||||
CCDS | CCDS46775 | ||||||||||||||||||||||
HPRD | 07183 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AF157483 AY501390 BC060794 CH471055 HQ692863 M57445 X04014 X07282 X56849 X77664 Y00291 | ||||||||||||||||||||||
GenPept | AAA58728 AAD45688 AAH60794 AAS85757 ADZ17374 CAA27637 CAA30262 CAA54740 CAA68398 EAW64355 | ||||||||||||||||||||||