Bos taurus Gene: EDNRB
Summary
InnateDB Gene IDBG-631994.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol EDNRB
Gene Name Endothelin B receptor
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000005299
Encoded Proteins
Endothelin B receptor
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000136160:
The protein encoded by this gene is a G protein-coupled receptor which activates a phosphatidylinositol-calcium second messenger system. Its ligand, endothelin, consists of a family of three potent vasoactive peptides: ET1, ET2, and ET3. Studies suggest that the multigenic disorder, Hirschsprung disease type 2, is due to mutations in the endothelin receptor type B gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 12:53310604-53407024
Strand Reverse strand
Band
Transcripts
ENSBTAT00000006979 ENSBTAP00000006979
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 6 interaction(s) predicted by orthology.
Predicted by orthology
Total 6 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004871 signal transducer activity
GO:0004930 G-protein coupled receptor activity
GO:0004962 endothelin receptor activity
GO:0005515 protein binding
GO:0017046 peptide hormone binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001755 neural crest cell migration
GO:0006885 regulation of pH
GO:0007165 signal transduction
GO:0007186 G-protein coupled receptor signaling pathway
GO:0007422 peripheral nervous system development
GO:0007497 posterior midgut development
GO:0008217 regulation of blood pressure
GO:0014043 negative regulation of neuron maturation
GO:0014826 vein smooth muscle contraction
GO:0030318 melanocyte differentiation
GO:0032269 negative regulation of cellular protein metabolic process
GO:0035645 enteric smooth muscle cell differentiation
GO:0042310 vasoconstriction
GO:0043473 pigmentation
GO:0048066 developmental pigmentation
GO:0048246 macrophage chemotaxis
GO:0048484 enteric nervous system development
Cellular Component
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
Gastrin-CREB signalling pathway via PKC and MAPK pathway
Peptide ligand-binding receptors pathway
Signaling by GPCR pathway
Signal Transduction pathway
G alpha (q) signalling events pathway
GPCR downstream signaling pathway
GPCR ligand binding pathway
Class A/1 (Rhodopsin-like receptors) pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
G alpha (q) signalling events pathway
Gastrin-CREB signalling pathway via PKC and MAPK pathway
Peptide ligand-binding receptors pathway
Class A/1 (Rhodopsin-like receptors) pathway
Signaling by GPCR pathway
Signal Transduction pathway
GPCR downstream signaling pathway
GPCR ligand binding pathway
GPCR downstream signaling pathway
Signaling by GPCR pathway
Class A/1 (Rhodopsin-like receptors) pathway
Gastrin-CREB signalling pathway via PKC and MAPK pathway
GPCR ligand binding pathway
Peptide ligand-binding receptors pathway
G alpha (q) signalling events pathway
Signal Transduction pathway
KEGG
Neuroactive ligand-receptor interaction pathway
Calcium signaling pathway pathway
Melanogenesis pathway
Calcium signaling pathway pathway
Melanogenesis pathway
Neuroactive ligand-receptor interaction pathway
INOH
PID NCI
Endothelins
Cross-References
SwissProt P28088
TrEMBL Q862I2
UniProt Splice Variant
Entrez Gene 281750
UniGene Bt.487
RefSeq NM_174309 XM_005213874
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL AB099006 BC120256 D10994 D90456
GenPept AAI20257 BAA01762 BAA14422 BAC56496
RNA Seq Atlas 281750