Homo sapiens Protein: RXFP3
Summary
InnateDB Protein IDBP-14872.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RXFP3
Protein Name relaxin/insulin-like family peptide receptor 3
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000328708
InnateDB Gene IDBG-14870 (RXFP3)
Protein Structure
UniProt Annotation
Function Receptor for RNL3/relaxin-3. Binding of the ligand inhibit cAMP accumulation. {ECO:0000269PubMed:14522968}.
Subcellular Localization Cell membrane; Multi-pass membrane protein.
Disease Associations
Tissue Specificity Expressed predominantly in brain regions. Highest expression in substantia nigra and pituitary, followed by hippocampus, spinal cord, amygdala, caudate nucleus and corpus callosum, quite low level in cerebellum. In peripheral tissues, relatively high levels in adrenal glands, low levels in pancreas, salivary gland, placenta, mammary gland and testis.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0004930 G-protein coupled receptor activity
GO:0008528 G-protein coupled peptide receptor activity
Biological Process
GO:0007186 G-protein coupled receptor signaling pathway
GO:0032467 positive regulation of cytokinesis
GO:0051482 positive regulation of cytosolic calcium ion concentration involved in phospholipase C-activating G-protein coupled signaling pathway
Cellular Component
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR000276 G protein-coupled receptor, rhodopsin-like
IPR017452 GPCR, rhodopsin-like, 7TM
PFAM PF00001
PRINTS PR00237
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9NSD7
PhosphoSite PhosphoSite-Q9NSD7
TrEMBL
UniProt Splice Variant
Entrez Gene 51289
UniGene Hs.170146
RefSeq NP_057652
HUGO HGNC:24883
OMIM 609445
CCDS CCDS3900
HPRD 17979
IMGT
EMBL AY236541 AY394501 BC113438 BC113440 D88437
GenPept AAI13439 AAI13441 AAO92063 AAQ92315 BAA93001