Ednrb (endothelin receptor type B) - Rat Genome Database

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Gene: Ednrb (endothelin receptor type B) Rattus norvegicus
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Symbol: Ednrb
Name: endothelin receptor type B
RGD ID: 2536
Description: Enables endothelin receptor activity and type 1 angiotensin receptor binding activity. Involved in several processes, including blood vessel diameter maintenance; cGMP-mediated signaling; and positive regulation of penile erection. Located in nuclear membrane. Used to study several diseases, including artery disease (multiple); lymphopenia; megacolon (multiple); portal hypertension; and type 2 diabetes mellitus. Biomarker of asthma; hepatopulmonary syndrome; and hypertension. Human ortholog(s) of this gene implicated in ABCD syndrome; Hirschsprung's disease; Waardenburg syndrome; Waardenburg syndrome type 4A; and asthma. Orthologous to human EDNRB (endothelin receptor type B); PARTICIPATES IN calcium/calmodulin dependent kinase signaling pathway; endothelin signaling pathway; inflammatory response pathway; INTERACTS WITH (R)-noradrenaline; (S)-colchicine; (S)-nicotine.
Type: protein-coding
RefSeq Status: PROVISIONAL
Previously known as: Ednra; endothelin B receptor; endothelin receptor; endothelin receptor non-selective type; endothelin-B receptor; ET-B; ET-BR; Etb
RGD Orthologs
Human
Mouse
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: Ednrbsl
Genetic Models: F344.AR-Ednrbsl/Hkv ; AR-Ednrbsl/Hkv ; LEH/Hkv ; LE.AR-Ednrbsl/Okkm ; AR-Ednrbsl/Okkm
Is Marker For: Strains:   DA   Sl   LE.AR-Ednrbsl/Okkm   AR-Ednrbsl/Okkm   SI-Tg(Ednrb)Ywa  
QTLs:   Scl1   BpQTLcluster12   Bp126   Gluco31  
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81587,055,490 - 87,086,765 (-)NCBIGRCr8
mRatBN7.21580,640,839 - 80,672,115 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1580,643,043 - 80,672,115 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1584,622,892 - 84,651,923 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01585,745,953 - 85,774,986 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01582,673,598 - 82,702,629 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01588,004,775 - 88,036,354 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1588,006,977 - 88,036,354 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01591,500,400 - 91,531,979 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41587,893,141 - 87,898,700 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11587,908,924 - 87,914,471 (-)NCBI
Celera1579,772,740 - 79,801,760 (-)NCBICelera
RH 3.4 Map15496.21RGD
Cytogenetic Map15q22NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Original Reference(s)
EdnrbRatasthma  ISORGD:105054892288 RGD 
EdnrbRatasthma  IEP 4892324mRNA:increased expression:bronchus, smooth muscle cellRGD 
EdnrbRatasthma  ISORGD:7360904892321DNA:polymorphism (human)RGD 
EdnrbRathepatopulmonary syndrome  IEP 4892290protein:increased expression:lungRGD 
EdnrbRatHirschsprung's disease treatmentIMP 628516 RGD 
EdnrbRatHirschsprung's disease  IAGP 6480215 RGD 
EdnrbRatHirschsprung's disease  IAGP 6480217 RGD 
EdnrbRatHirschsprung's disease  ISORGD:7360901601008DNA:point mutation:exon:W276CRGD 
EdnrbRatHirschsprung's disease  IAGP 1342447 RGD 
EdnrbRathypertension  IEP 4892284associated with UremiaRGD 
EdnrbRathypertension  IMP 628518 RGD 
EdnrbRatHypopigmentation  IAGP 10755346compared to LE/Hkv.AR-EdnrbslRGD 
EdnrbRatlymphopenia  IAGP 7207471 RGD 
EdnrbRatmegacolon  IAGP 628515 RGD 
EdnrbRatmyocardial infarction  IDA 1580948 RGD 
EdnrbRatMyocardial Ischemia  ISORGD:7360901580946 RGD 
EdnrbRatMyocardial Reperfusion Injury  IMP 4892332 RGD 
EdnrbRatOptic Nerve Injuries  IEP 4892579mRNA:increased expression:retinaRGD 
EdnrbRatPerinatal Death  IAGP 628515 RGD 
EdnrbRatportal hypertension  IMP 4892595 RGD 
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Original Reference(s)
EdnrbRatABCD syndrome  ISORGD:7360908554872ClinVar Annotator: match by term: ABCD syndromeClinVarPMID:10528251|PMID:11891690|PMID:20127975|PMID:24033266|PMID:25741868|PMID:26100139|PMID:26467025|PMID:28492532|PMID:30394532|PMID:7778600|PMID:8001159
EdnrbRatautosomal recessive nonsyndromic deafness  ISORGD:7360908554872ClinVar Annotator: match by term: Autosomal recessive nonsyndromic deafnessClinVarPMID:14633923|PMID:16944573|PMID:17554617|PMID:18162831|PMID:20127975|PMID:25741868|PMID:29106856|PMID:30303587|PMID:30936914|PMID:31240788|PMID:32747562|PMID:33095980|PMID:35790984
EdnrbRatchromosome 13q14 deletion syndrome  ISORGD:7360908554872ClinVar Annotator: match by term: Chromosome 13q14 deletion syndromeClinVar 
EdnrbRatgenetic disease  ISORGD:7360908554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:14633923|PMID:16944573|PMID:17554617|PMID:18162831|PMID:20127975|PMID:24033266|PMID:25741868|PMID:28492532|PMID:29106856|PMID:30303587|PMID:30936914|PMID:31240788|PMID:32747562|PMID:33095980|PMID:35790984
EdnrbRatHearing Loss  ISORGD:7360908554872ClinVar Annotator: match by term: Hearing impairment | ClinVar Annotator: match by term: Nonsyndromic Hearing more ...ClinVarPMID:14633923|PMID:16944573|PMID:17554617|PMID:18162831|PMID:20127975|PMID:25741868|PMID:29106856|PMID:30303587|PMID:30311386|PMID:30936914|PMID:31240788|PMID:32747562|PMID:33095980|PMID:35790984
EdnrbRatHirschsprung's disease  ISORGD:7360908554872ClinVar Annotator: match by term: Hirschsprung Disease, Recessive | ClinVar Annotator: match by term: Hirschsprung more ...ClinVarPMID:10090908|PMID:10458491|PMID:10528251|PMID:10664228|PMID:10874640|PMID:12628594|PMID:14633923|PMID:16145050|PMID:16199547|PMID:16518596|PMID:16944573|PMID:16954478|PMID:17011274|PMID:17223014|PMID:17554617|PMID:17618893|PMID:18162831|PMID:18633623|PMID:18758497|PMID:19320733|PMID:20009762|PMID:20127975|PMID:21507037|PMID:22993632|PMID:22995991|PMID:24033266|PMID:24311220|PMID:25741868|PMID:26467025|PMID:27535533|PMID:27639823|PMID:28236341|PMID:28492532|PMID:29106856|PMID:29407415|PMID:30218169|PMID:30303587|PMID:30394532|PMID:30936914|PMID:31240788|PMID:32747562|PMID:33095980|PMID:34422713|PMID:35790984|PMID:8001158|PMID:8001159|PMID:8852658|PMID:8852659|PMID:8852660|PMID:9760196
EdnrbRatmitochondrial DNA depletion syndrome 12a  ISORGD:7360908554872ClinVar Annotator: match by term: Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominantClinVarPMID:10090908|PMID:10874640|PMID:16145050|PMID:16954478|PMID:19320733|PMID:20009762|PMID:21507037|PMID:22993632|PMID:22995991|PMID:24033266|PMID:25741868|PMID:26467025|PMID:27535533|PMID:28492532|PMID:29407415|PMID:8852659
EdnrbRatneuronal ceroid lipofuscinosis  ISORGD:7360908554872ClinVar Annotator: match by term: Neuronal ceroid lipofuscinosisClinVarPMID:10528251|PMID:20127975|PMID:20157158|PMID:22589734|PMID:28492532|PMID:30394532|PMID:31406620|PMID:32393339|PMID:8001159
EdnrbRatTotal Intestinal Aganglionosis  ISORGD:7360908554872ClinVar Annotator: match by term: Aganglionosis, total intestinalClinVarPMID:14633923|PMID:16944573|PMID:17554617|PMID:18162831|PMID:20127975|PMID:25741868|PMID:29106856|PMID:30303587|PMID:30936914|PMID:31240788|PMID:32747562|PMID:33095980|PMID:35790984
EdnrbRatVan der Hoeve Halbertsma Waardenburg Gualdi Syndrome  ISORGD:7360908554872ClinVar Annotator: match by term: Mende SyndromeClinVarPMID:25741868|PMID:30311386
EdnrbRatWaardenburg syndrome  ISORGD:7360908554872ClinVar Annotator: match by term: Waardenburg syndromeClinVarPMID:24033266|PMID:25741868|PMID:28492532|PMID:30311386
EdnrbRatWaardenburg syndrome type 2A  ISORGD:7360908554872ClinVar Annotator: match by term: Waardenburg syndrome type 2AClinVarPMID:10090908|PMID:10874640|PMID:16145050|PMID:16954478|PMID:19320733|PMID:20009762|PMID:21507037|PMID:22993632|PMID:22995991|PMID:24033266|PMID:25741868|PMID:26467025|PMID:27535533|PMID:28492532|PMID:29407415|PMID:8852659
EdnrbRatWaardenburg Syndrome Type 4  ISORGD:7360908554872ClinVar Annotator: match by term: Hirschsprung disease with pigmentary anomalyClinVarPMID:14633923|PMID:16944573|PMID:17554617|PMID:18162831|PMID:20127975|PMID:25741868|PMID:29106856|PMID:30303587|PMID:30311386|PMID:30936914|PMID:31240788|PMID:32747562|PMID:33095980|PMID:35790984
EdnrbRatWaardenburg syndrome type 4A  ISORGD:7360908554872ClinVar Annotator: match by term: Waardenburg syndrome type 4AClinVarPMID:10090908|PMID:10458491|PMID:10528251|PMID:10664228|PMID:10874640|PMID:11891690|PMID:14633923|PMID:16145050|PMID:16944573|PMID:16954478|PMID:17011274|PMID:17554617|PMID:18162831|PMID:19320733|PMID:20009762|PMID:20127975|PMID:21507037|PMID:22993632|PMID:22995991|PMID:24033266|PMID:24311220|PMID:25741868|PMID:26467025|PMID:27535533|PMID:28236341|PMID:28492532|PMID:29106856|PMID:29407415|PMID:30303587|PMID:30311386|PMID:30394532|PMID:30936914|PMID:31240788|PMID:32747562|PMID:33095980|PMID:35790984|PMID:7778600|PMID:8001158|PMID:8001159|PMID:8634719|PMID:8852659|PMID:8852660
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Original Reference(s)
EdnrbRatABCD syndrome  ISORGD:73609011554173CTD Direct Evidence: marker/mechanismCTD 
EdnrbRatBreast Neoplasms  ISORGD:73609011554173CTD Direct Evidence: therapeuticCTDPMID:16244791
EdnrbRatcongestive heart failure  ISORGD:73609011554173CTD Direct Evidence: marker/mechanismCTDPMID:28095452
EdnrbRatDiaphragmatic Hernia  ISORGD:73609011554173CTD Direct Evidence: marker/mechanismCTDPMID:10693666
EdnrbRatHirschsprung's disease  ISORGD:73609011554173CTD Direct Evidence: marker/mechanismCTDPMID:8896568
EdnrbRatNeoplasm Invasiveness  ISORGD:73609011554173CTD Direct Evidence: marker/mechanismCTDPMID:26213588
EdnrbRatnephrosis  ISORGD:73609011554173CTD Direct Evidence: marker/mechanismCTDPMID:7756592
EdnrbRatpulmonary hypertension  ISORGD:73609011554173CTD Direct Evidence: marker/mechanismCTDPMID:15927975
EdnrbRatSubarachnoid Hemorrhage  ISORGD:73609011554173CTD Direct Evidence: marker/mechanismCTDPMID:8587695
EdnrbRattype 2 diabetes mellitus  ISORGD:73609011554173CTD Direct Evidence: marker/mechanismCTDPMID:16387788
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EdnrbRatHirschsprung's disease  ISSRGD:1050513592920OMIM:600156 | OMIM:606874 | OMIM:606875 | OMIM:608462 | OMIM:611644MouseDO 
EdnrbRatWaardenburg syndrome type 4A  ISSRGD:1050513592920OMIM:277580MouseDO 
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Original Reference(s)
EdnrbRatABCD syndrome  ISORGD:7360907240710 OMIM 
EdnrbRatHirschsprung's disease  ISORGD:7360907240710 OMIM 
EdnrbRatWaardenburg syndrome type 4A  ISORGD:7360907240710 OMIM 

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Original Reference(s)
EdnrbRat(-)-epigallocatechin 3-gallate multiple interactionsISORGD:7360906480464[potassium chromate(VI) co-treated with epigallocatechin gallate] results in decreased expression of EDNRB mRNACTDPMID:22079256
EdnrbRat(R)-noradrenaline multiple interactionsEXP 6480464[EDN1 protein binds to and results in increased activity of EDNRB protein] which results in more ...CTDPMID:16023617
EdnrbRat(S)-colchicine increases expressionEXP 6480464Colchicine results in increased expression of EDNRB mRNACTDPMID:20624997
EdnrbRat(S)-nicotine increases activityEXP 6480464Nicotine results in increased activity of EDNRB proteinCTDPMID:21316381
EdnrbRat1,2-dimethylhydrazine decreases expressionISORGD:1050564804641,2-Dimethylhydrazine results in decreased expression of EDNRB mRNACTDPMID:22206623
EdnrbRat17alpha-ethynylestradiol multiple interactionsISORGD:7360906480464[Ethinyl Estradiol co-treated with Cholic Acids] affects the expression of EDNRB mRNACTDPMID:27344345
EdnrbRat17beta-estradiol multiple interactionsISORGD:7360906480464[Estradiol co-treated with Progesterone] results in decreased expression of EDNRB mRNACTDPMID:20660070
EdnrbRat17beta-estradiol affects expressionEXP 6480464Estradiol affects the expression of EDNRB mRNACTDPMID:32145629
EdnrbRat2,3,7,8-tetrachlorodibenzodioxine decreases expressionISORGD:7360906480464Tetrachlorodibenzodioxin results in decreased expression of EDNRB mRNACTDPMID:20106945
EdnrbRat2,3,7,8-tetrachlorodibenzodioxine affects expressionEXP 6480464Tetrachlorodibenzodioxin affects the expression of EDNRB mRNACTDPMID:34747641
EdnrbRat2,3,7,8-tetrachlorodibenzodioxine increases expressionISORGD:7360906480464Tetrachlorodibenzodioxin results in increased expression of EDNRB mRNACTDPMID:25445724
EdnrbRat2,3,7,8-tetrachlorodibenzodioxine multiple interactionsISORGD:7360906480464AHR gene SNP affects the reaction [Tetrachlorodibenzodioxin results in increased expression of EDNRB mRNA]CTDPMID:25445724
EdnrbRat2,3,7,8-tetrachlorodibenzodioxine affects expressionISORGD:7360906480464Tetrachlorodibenzodioxin affects the expression of EDNRB mRNACTDPMID:22298810
EdnrbRat2,3,7,8-tetrachlorodibenzodioxine increases expressionISORGD:105056480464Tetrachlorodibenzodioxin results in increased expression of EDNRB mRNACTDPMID:19465110
EdnrbRat2,4-dibromophenyl 2,4,5-tribromophenyl ether affects expressionISORGD:1050564804642,2',4,4',5-brominated diphenyl ether affects the expression of EDNRB mRNACTDPMID:38648751
EdnrbRat2-acetyl-1-alkyl-sn-glycero-3-phosphocholine multiple interactionsEXP 6480464EDNRB protein affects the reaction [Carbon Tetrachloride promotes the reaction [EDN1 protein results in increased more ...CTDPMID:18205269
EdnrbRat2-butoxyethanol increases expressionISORGD:105056480464n-butoxyethanol results in increased expression of EDNRB mRNACTDPMID:19812364
EdnrbRat2-hydroxypropanoic acid decreases expressionISORGD:7360906480464Lactic Acid results in decreased expression of EDNRB mRNACTDPMID:30851411
EdnrbRat2-palmitoylglycerol increases expressionISORGD:73609064804642-palmitoylglycerol results in increased expression of EDNRB mRNACTDPMID:37199045
EdnrbRat3'-amino-3'-deoxy-N(6),N(6)-dimethyladenosine multiple interactionsEXP 6480464Methylprednisolone inhibits the reaction [Puromycin Aminonucleoside results in increased expression of EDNRB mRNA]CTDPMID:7756592

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Biological Process
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Original Reference(s)
EdnrbRataldosterone metabolic process involved_inISORGD:105051624291MGI:3693642 PMID:16868309RGDPMID:16868309
EdnrbRataldosterone metabolic process involved_inIEAUniProtKB:P48302|ensembl:ENSMUSP000000227181600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatblood circulation involved_inIEAARBA:ARBA000290441600115GO_REF:0000117UniProtGO_REF:0000117
EdnrbRatcalcium ion transmembrane transport involved_inISORGD:105051624291MGI:105923 PMID:24722437RGDPMID:24722437
EdnrbRatcalcium ion transmembrane transport involved_inIEAUniProtKB:P48302|ensembl:ENSMUSP000000227181600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatcalcium-mediated signaling involved_inISSUniProtKB:P245301600115GO_REF:0000024UniProtGO_REF:0000024
EdnrbRatcalcium-mediated signaling involved_inIEAUniProtKB:P24530|ensembl:ENSP000004935271600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatcalcium-mediated signaling involved_inISORGD:7360901624291 PMID:28236341RGDPMID:28236341
EdnrbRatcanonical Wnt signaling pathway involved_inISORGD:105051624291MGI:105923 PMID:24722437RGDPMID:24722437
EdnrbRatcanonical Wnt signaling pathway involved_inIEAUniProtKB:P48302|ensembl:ENSMUSP000000227181600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatcellular response to lipopolysaccharide  IEP 4892289 RGD 
EdnrbRatcGMP-mediated signaling  IMP 4892585 RGD 
EdnrbRatchordate pharynx development involved_inISORGD:105051624291 PMID:18199583RGDPMID:18199583
EdnrbRatchordate pharynx development involved_inIEAUniProtKB:P48302|ensembl:ENSMUSP000000227181600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatdevelopmental pigmentation acts_upstream_of_or_withinIEAUniProtKB:P48302|ensembl:ENSMUSP000000227181600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatdevelopmental pigmentation acts_upstream_of_or_withinISORGD:105051624291MGI:1856149 PMID:15322542RGDPMID:15322542
EdnrbRatdevelopmental pigmentation involved_inIBAMGI:102720|PANTHER:PTN002517505|RGD:2536|ZFIN:ZDB-GENE-010906-2|ZFIN:ZDB-GENE-980526-161600115GO_REF:0000033GO_CentralGO_REF:0000033
EdnrbRatendothelin receptor signaling pathway involved_inISORGD:7360901624291 PMID:1713452, PMID:19767294, PMID:28236341RGDPMID:1713452|PMID:19767294|PMID:28236341
EdnrbRatendothelin receptor signaling pathway involved_inIEAUniProtKB:P24530|ensembl:ENSP000004935271600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatendothelin receptor signaling pathway involved_inIBAMGI:102720|MGI:105923|PANTHER:PTN002517505|UniProtKB:P245301600115GO_REF:0000033GO_CentralGO_REF:0000033
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Cellular Component

  
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EdnrbRatmembrane located_inIEAInterPro:IPR000276|InterPro:IPR000499|InterPro:IPR001112|InterPro:IPR0174521600115GO_REF:0000002InterProGO_REF:0000002
EdnrbRatmembrane located_inIEAUniProtKB-KW:KW-04721600115GO_REF:0000043UniProtGO_REF:0000043
EdnrbRatnuclear membrane  IDA 1581838 RGD 
EdnrbRatplasma membrane located_inIEAUniProtKB-KW:KW-10031600115GO_REF:0000043UniProtGO_REF:0000043
EdnrbRatplasma membrane located_inIEAUniProtKB:P24530|ensembl:ENSP000004935271600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatplasma membrane is_active_inIBAPANTHER:PTN002517505|RGD:2535|UniProtKB:P245301600115GO_REF:0000033GO_CentralGO_REF:0000033
EdnrbRatplasma membrane located_inIEAUniProtKB-SubCell:SL-00391600115GO_REF:0000044UniProtGO_REF:0000044
EdnrbRatplasma membrane located_inISORGD:7360901624291 PMID:28236341RGDPMID:28236341

Molecular Function
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EdnrbRatendothelin receptor activity  TAS 628459 RGD 
EdnrbRatendothelin receptor activity enablesIEAUniProtKB:P24530|ensembl:ENSP000004935271600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatendothelin receptor activity enablesIEAInterPro:IPR000499|InterPro:IPR0011121600115GO_REF:0000002InterProGO_REF:0000002
EdnrbRatendothelin receptor activity enablesIEAUniProtKB:P48302|ensembl:ENSMUSP000000227181600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatendothelin receptor activity enablesISORGD:105051624291MGI:1857161 PMID:11413164, PMID:12441350, PMID:24722437RGDPMID:11413164|PMID:12441350|PMID:24722437
EdnrbRatendothelin receptor activity enablesIBAMGI:102720|MGI:105923|PANTHER:PTN002517505|RGD:2535|RGD:2536|UniProtKB:P245301600115GO_REF:0000033GO_CentralGO_REF:0000033
EdnrbRatendothelin receptor activity enablesISORGD:7360901624291 PMID:1713452, PMID:19767294, PMID:28236341RGDPMID:1713452|PMID:19767294|PMID:28236341
EdnrbRatendothelin receptor activity  IDA 730808 RGD 
EdnrbRatG protein-coupled receptor activity  TAS 628459 RGD 
EdnrbRatG protein-coupled receptor activity enablesIEAInterPro:IPR0002761600115GO_REF:0000002InterProGO_REF:0000002
EdnrbRatG protein-coupled receptor activity enablesIEAUniProtKB-KW:KW-02971600115GO_REF:0000043UniProtGO_REF:0000043
EdnrbRatpeptide hormone binding enablesISORGD:7360901624291UniProtKB:P05305|UniProtKB:P14138|UniProtKB:P20800 PMID:1713452RGDPMID:1713452
EdnrbRatpeptide hormone binding enablesIEAUniProtKB:P24530|ensembl:ENSP000004935271600115GO_REF:0000107EnsemblGO_REF:0000107
EdnrbRatprotein binding enablesISORGD:7360901624291UniProtKB:P05305 PMID:23597562RGDPMID:23597562
EdnrbRatprotein binding enablesISORGD:105051624291PR:P22387 PMID:12441350RGDPMID:12441350
EdnrbRattype 1 angiotensin receptor binding  IPIRGD:20701581862 RGD 
EdnrbRattype 1 angiotensin receptor binding  IPIRGD:20711581862 RGD 
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RGD Manual Annotations


  
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With
Reference
Notes
Source
Original Reference(s)
EdnrbRatcalcium/calmodulin dependent kinase signaling pathway  IMP 1581866 RGD 
EdnrbRatendothelin signaling pathway  IMP 4892591 RGD 
EdnrbRatinflammatory response pathway  IMP 4892591 RGD 

Imported Annotations - KEGG (archival)

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
EdnrbRatcalcium/calcium-mediated signaling pathway   IEA 6907045 KEGGrno:04020

Imported Annotations - PID (archival)

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
EdnrbRatendothelin signaling pathway  ISORGD:7360906484113 PIDPID:200005

1 to 20 of 78 rows
#
Reference Title
Reference Citation
1. Developmental changes in the functional, biochemical and molecular properties of rat bladder endothelin receptors. Afiatpour P, etal., Naunyn Schmiedebergs Arch Pharmacol. 2003 May;367(5):462-72. Epub 2003 Apr 17.
2. Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease. Attie T, etal., Hum Mol Genet. 1995 Dec;4(12):2407-9.
3. ETA receptor-mediated Ca2+ signaling in thin descending limbs of Henle's loop: impairment in genetic hypertension. Bailey MA, etal., Kidney Int. 2003 Apr;63(4):1276-84.
4. Endothelin-1 receptor subtypes expression and binding in a perfused rat model of myocardial infarction. Bikhazi AB, etal., Comp Biochem Physiol C Toxicol Pharmacol. 2003 Jan;134(1):35-43.
5. Functional endothelin receptors are present on nuclei in cardiac ventricular myocytes. Boivin B, etal., J Biol Chem. 2003 Aug 1;278(31):29153-63. Epub 2003 May 19.
6. Murine and rat cavernosal responses to endothelin-1 and urotensin-II Vasoactive Peptide Symposium. Carneiro FS, etal., J Am Soc Hypertens. 2008 Nov;2(6):439-447.
7. ETA receptor-mediated Ca2+ mobilisation in H9c2 cardiac cells. Ceccarelli F, etal., Biochem Pharmacol 2003 Mar 1;65(5):783-93.
8. Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) rat. Ceccherini I, etal., Hum Mol Genet 1995 Nov;4(11):2089-96.
9. Effects of chronic cold exposure on the endothelin system. Chen GF and Sun Z, J Appl Physiol. 2006 May;100(5):1719-26. Epub 2005 Dec 29.
10. Endothelins as pronociceptive mediators of the rat trigeminal system: role of ETA and ETB receptors. Chichorro JG, etal., Brain Res. 2010 Jul 23;1345:73-83. Epub 2010 May 5.
11. Endothelin-1 impairs alveolar epithelial function via endothelial ETB receptor. Comellas AP, etal., Am J Respir Crit Care Med. 2009 Jan 15;179(2):113-22. Epub 2008 Oct 23.
12. Increased ET-1 and reduced ET(B) receptor expression in uremic hypertensive rats. D'Amours M, etal., Clin Exp Hypertens. 2010 Jan;32(1):61-9.
13. Lymphopenia in Ednrb-deficient rat was strongly modified by genetic background. Dang R, etal., Biomed Res. 2012;33(4):249-53.
14. QTL analysis identifies a modifier locus of aganglionosis in the rat model of Hirschsprung disease carrying Ednrb(sl) mutations. Dang R, etal., PLoS One. 2011;6(11):e27902. Epub 2011 Nov 22.
15. Genetic background strongly modifies the severity of symptoms of Hirschsprung disease, but not hearing loss in rats carrying Ednrb(sl) mutations. Dang R, etal., PLoS One. 2011;6(9):e24086. Epub 2011 Sep 7.
16. Genetic mapping of two new blood pressure quantitative trait loci in the rat by genotyping endothelin system genes. Deng AY, etal., J Clin Invest 1994 Jun;93(6):2701-9
17. Upregulation of endothelin receptors A and B in the nitrofen induced hypoplastic lung occurs early in gestation. Dingemann J, etal., Pediatr Surg Int. 2010 Jan;26(1):65-9.
18. Endotoxin causes pulmonary hypertension by upregulating smooth muscle endothelin type-B receptors: role of aldose reductase. Dschietzig T, etal., Shock. 2008 Aug;30(2):189-96.
19. Central endothelin ET(B) receptors mediate IL-1-dependent fever induced by preformed pyrogenic factor and corticotropin-releasing factor in the rat. Fabricio AS, etal., Am J Physiol Regul Integr Comp Physiol. 2006 Jan;290(1):R164-71. Epub 2005 Aug 25.
20. NAADP-induced Ca(2+ signaling in response to endothelin is via the receptor subtype B and requires the integrity of lipid rafts/caveolae. Gambara G, etal., J Cell Physiol. 2008 Aug;216(2):396-404.
1 to 20 of 78 rows
1 to 10 of 14 rows
PMID:1312429   PMID:1713452   PMID:2379821   PMID:8371713   PMID:8582288   PMID:8982507   PMID:9012511   PMID:10021336   PMID:10591209   PMID:10626068   PMID:11413164   PMID:11834512  
PMID:11897624   PMID:11910302   PMID:12088756   PMID:12164874   PMID:12207323   PMID:12421649   PMID:12441350   PMID:12668144   PMID:12686728   PMID:12713865   PMID:12750545   PMID:12813000  
PMID:12919946   PMID:14988072   PMID:15194452   PMID:15280069   PMID:15311109   PMID:15322542   PMID:15344879   PMID:15464196   PMID:15761039   PMID:15838256   PMID:15838268   PMID:15838271  
PMID:15838321   PMID:15838330   PMID:15838350   PMID:15838354   PMID:15838359   PMID:15838360   PMID:15838363   PMID:16144989   PMID:16341592   PMID:16463654   PMID:16806184   PMID:16947426  
PMID:17337507   PMID:17345093   PMID:17400719   PMID:17495482   PMID:17522762   PMID:17626731   PMID:17632282   PMID:17664390   PMID:17670915   PMID:17873013   PMID:17892518   PMID:18205269  
PMID:18242601   PMID:18281380   PMID:18287215   PMID:18424628   PMID:18469849   PMID:18516102   PMID:18518881   PMID:18524860   PMID:18547994   PMID:18567602   PMID:18758505   PMID:18793415  
PMID:19111903   PMID:19157542   PMID:19196949   PMID:19297422   PMID:19353416   PMID:19535675   PMID:19628575   PMID:19767294   PMID:19945955   PMID:20008273   PMID:20026178   PMID:20399772  
PMID:20716444   PMID:20844020   PMID:21035524   PMID:21228598   PMID:21428728   PMID:21536992   PMID:21801590   PMID:22007724   PMID:22198335   PMID:22198514   PMID:22258095   PMID:22391414  
PMID:22457360   PMID:22585122   PMID:22787113   PMID:22848635   PMID:22916224   PMID:22952915   PMID:23047940   PMID:23086942   PMID:23351051   PMID:23370722   PMID:23396520   PMID:23436727  
PMID:23599626   PMID:23646960   PMID:23875673   PMID:23988741   PMID:24144054   PMID:24462674   PMID:24467585   PMID:24503339   PMID:24582810   PMID:24731444   PMID:24779608   PMID:24815227  
1 to 10 of 14 rows



Ednrb
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81587,055,490 - 87,086,765 (-)NCBIGRCr8
mRatBN7.21580,640,839 - 80,672,115 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1580,643,043 - 80,672,115 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1584,622,892 - 84,651,923 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01585,745,953 - 85,774,986 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01582,673,598 - 82,702,629 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01588,004,775 - 88,036,354 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1588,006,977 - 88,036,354 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01591,500,400 - 91,531,979 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41587,893,141 - 87,898,700 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11587,908,924 - 87,914,471 (-)NCBI
Celera1579,772,740 - 79,801,760 (-)NCBICelera
RH 3.4 Map15496.21RGD
Cytogenetic Map15q22NCBI
EDNRB
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381377,895,487 - 77,975,527 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1377,895,481 - 77,975,529 (-)EnsemblGRCh38hg38GRCh38
GRCh371378,469,622 - 78,549,662 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361377,367,617 - 77,447,665 (-)NCBINCBI36Build 36hg18NCBI36
Build 341377,368,543 - 77,390,935NCBI
Celera1359,367,540 - 59,390,895 (-)NCBICelera
Cytogenetic Map13q22.3NCBI
HuRef1359,168,348 - 59,248,390 (-)NCBIHuRef
CHM1_11378,436,966 - 78,516,998 (-)NCBICHM1_1
T2T-CHM13v2.01377,120,409 - 77,200,427 (-)NCBIT2T-CHM13v2.0
Ednrb
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3914104,052,055 - 104,081,764 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl14104,052,061 - 104,081,838 (-)EnsemblGRCm39 Ensembl
GRCm3814103,814,615 - 103,844,508 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl14103,814,625 - 103,844,402 (-)EnsemblGRCm38mm10GRCm38
MGSCv3714104,213,842 - 104,243,390 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3614102,700,305 - 102,729,375 (-)NCBIMGSCv36mm8
Celera14102,434,540 - 102,464,042 (-)NCBICelera
Cytogenetic Map14E2.3NCBI
cM Map1453.05NCBI
Ednrb
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540429,394,164 - 29,425,358 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540429,394,253 - 29,425,358 (+)NCBIChiLan1.0ChiLan1.0
EDNRB
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21479,464,042 - 79,488,264 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11378,060,299 - 78,084,570 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01359,112,349 - 59,136,615 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11378,153,026 - 78,177,281 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1378,153,020 - 78,177,286 (-)Ensemblpanpan1.1panPan2
EDNRB
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12231,415,324 - 31,438,772 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2231,417,308 - 31,437,587 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2231,277,699 - 31,297,545 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02231,733,123 - 31,756,544 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2231,733,292 - 31,756,408 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12231,396,562 - 31,416,398 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02231,434,803 - 31,454,631 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02231,507,052 - 31,526,893 (-)NCBIUU_Cfam_GSD_1.0
Ednrb
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404945128,029,566 - 128,061,207 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365113,446,839 - 3,478,434 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365113,446,864 - 3,478,434 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
EDNRB
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1150,072,554 - 50,102,884 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11150,073,300 - 50,102,879 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21154,689,465 - 54,718,898 (-)NCBISscrofa10.2Sscrofa10.2susScr3
EDNRB
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1356,969,493 - 56,993,719 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl356,969,101 - 56,992,731 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604613,190,167 - 13,214,545 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ednrb
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462475122,459,584 - 22,491,606 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462475122,459,613 - 22,491,409 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

.
Variants in Ednrb
108 total Variants

Predicted Target Of
Summary Value
Count of predictions:222
Count of miRNA genes:153
Interacting mature miRNAs:170
Transcripts:ENSRNOT00000014747
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


1 to 10 of 24 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
731177Uae26Urinary albumin excretion QTL 262.40.025urine albumin amount (VT:0002871)urine albumin excretion rate (CMO:0000757)1567588667101769107Rat
1300144Rf23Renal function QTL 233.61renal blood flow trait (VT:2000006)absolute change in renal vascular resistance (CMO:0001900)154063126898288169Rat
1576315Schws6Schwannoma susceptibility QTL 60.0069nervous system integrity trait (VT:0010566)post-insult time of death (CMO:0002005)155380615298806152Rat
1549844Bss7Bone structure and strength QTL 76.4femur strength trait (VT:0010010)femur midshaft polar moment of inertia (CMO:0001669)1575788062101769107Rat
61477Aia4Adjuvant induced arthritis QTL 43joint integrity trait (VT:0010548)joint inflammation composite score (CMO:0000919)155559608991365858Rat
2300326Plaw1Placental weight QTL 1150.005placenta mass (VT:0004257)placenta wet weight (CMO:0002088)1568327165100062518Rat
70182BpQTLcluster12Blood pressure QTL cluster 123.53arterial blood pressure trait (VT:2000000)absolute change in mean arterial blood pressure (CMO:0000533)157369065795018120Rat
152025253Hrtrt24Heart rate QTL 243.82heart pumping trait (VT:2000009)152788577486257085Rat
70155Gcs1Gastric cancer susceptibility QTL13.8stomach morphology trait (VT:0000470)stomach tumor susceptibility score (CMO:0002043)1576306099101769107Rat
1582227Gluco30Glucose level QTL 303.60.0003blood glucose amount (VT:0000188)absolute change in blood glucose level area under curve (CMO:0002034)152803066582262678Rat

1 to 10 of 24 rows
D15Mco2  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21580,640,428 - 80,640,727 (+)MAPPERmRatBN7.2
mRatBN7.21580,640,501 - 80,640,727 (+)MAPPERmRatBN7.2
Rnor_6.01588,004,438 - 88,004,663NCBIRnor6.0
Rnor_6.01588,004,206 - 88,004,663NCBIRnor6.0
Rnor_5.01591,500,063 - 91,500,288UniSTSRnor5.0
Rnor_5.01591,499,831 - 91,500,288UniSTSRnor5.0
RGSC_v3.41587,890,620 - 87,890,845UniSTSRGSC3.4
RGSC_v3.41587,890,619 - 87,890,845RGDRGSC3.4
RGSC_v3.11587,906,399 - 87,906,625RGD
Celera1579,770,219 - 79,770,444UniSTS
Cytogenetic Map15q21-q22UniSTS
D15Mco3  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21580,645,554 - 80,645,729 (+)MAPPERmRatBN7.2
Rnor_6.01588,009,405 - 88,009,579NCBIRnor6.0
Rnor_5.01591,505,030 - 91,505,204UniSTSRnor5.0
RGSC_v3.41587,895,670 - 87,895,844UniSTSRGSC3.4
Celera1579,775,226 - 79,775,400UniSTS
Cytogenetic Map15q21-q22UniSTS
D15Wox13  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21580,648,147 - 80,648,395 (+)MAPPERmRatBN7.2
Rnor_6.01588,012,000 - 88,012,247NCBIRnor6.0
Rnor_5.01591,507,625 - 91,507,872UniSTSRnor5.0
RGSC_v3.41587,898,265 - 87,898,512UniSTSRGSC3.4
Celera1579,777,821 - 79,778,067UniSTS
Cytogenetic Map15q21-q22UniSTS
D15Ulb3  
Rat AssemblyChrPosition (strand)SourceJBrowse
GRCr81587,061,214 - 87,061,500 (+)Marker Load Pipeline
mRatBN7.21580,646,566 - 80,646,850 (+)MAPPERmRatBN7.2
Rnor_6.01588,010,417 - 88,010,700NCBIRnor6.0
Rnor_5.01591,506,042 - 91,506,325UniSTSRnor5.0
RGSC_v3.41587,896,682 - 87,896,965UniSTSRGSC3.4
Celera1579,776,238 - 79,776,521UniSTS
Cytogenetic Map15q21-q22UniSTS
PMC24270P1  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21580,643,379 - 80,643,591 (+)MAPPERmRatBN7.2
Rnor_6.01588,007,314 - 88,007,525NCBIRnor6.0
Rnor_5.01591,502,939 - 91,503,150UniSTSRnor5.0
RGSC_v3.41587,893,496 - 87,893,707UniSTSRGSC3.4
Celera1579,773,095 - 79,773,306UniSTS
Cytogenetic Map15q21-q22UniSTS
AA818970  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21580,670,939 - 80,671,119 (+)MAPPERmRatBN7.2
Rnor_6.01588,035,179 - 88,035,358NCBIRnor6.0
Rnor_5.01591,530,804 - 91,530,983UniSTSRnor5.0
Celera1579,800,585 - 79,800,764UniSTS
RH 3.4 Map15498.61UniSTS
Cytogenetic Map15q21-q22UniSTS
EDNRB-2  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21580,648,543 - 80,649,972 (+)MAPPERmRatBN7.2
Rnor_6.01588,012,396 - 88,013,824NCBIRnor6.0
Rnor_5.01591,508,021 - 91,509,449UniSTSRnor5.0
Celera1579,778,216 - 79,779,644UniSTS
Cytogenetic Map15q21-q22UniSTS


The following Strains have been annotated to Ednrb
AR-Ednrbsl/Okkm     DA     LE.AR-Ednrbsl/Okkm     SI-Tg(Ednrb)Ywa     Sl    


This gene Ednrb is modified in the following models/strains:




alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
nervous system
renal system
reproductive system
respiratory system
9 11 49 113 91 90 59 25 59 6 218 97 93 45 60 31



Ensembl Acc Id: ENSRNOT00000014747   ⟹   ENSRNOP00000014747
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl1580,643,043 - 80,672,115 (-)Ensembl
Rnor_6.0 Ensembl1588,006,977 - 88,036,354 (-)Ensembl
RefSeq Acc Id: NM_017333   ⟹   NP_059029
RefSeq Status: PROVISIONAL
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81587,057,673 - 87,086,765 (-)NCBI
mRatBN7.21580,643,025 - 80,672,115 (-)NCBI
Rnor_6.01588,006,959 - 88,036,354 (-)NCBI
Rnor_5.01591,500,400 - 91,531,979 (-)NCBI
RGSC_v3.41587,893,141 - 87,898,700 (-)RGD
Celera1579,772,740 - 79,801,760 (-)RGD
Sequence:
RefSeq Acc Id: XM_006252431   ⟹   XP_006252493
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81587,055,490 - 87,086,257 (-)NCBI
mRatBN7.21580,640,839 - 80,671,537 (-)NCBI
Rnor_6.01588,004,775 - 88,036,106 (-)NCBI
Rnor_5.01591,500,400 - 91,531,979 (-)NCBI
Sequence:
RefSeq Acc Id: NP_059029   ⟸   NM_017333
- Peptide Label: precursor
- UniProtKB: P21451 (UniProtKB/Swiss-Prot),   A6HUA5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006252493   ⟸   XM_006252431
- Peptide Label: isoform X1
- UniProtKB: P21451 (UniProtKB/Swiss-Prot),   A6HUA5 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSRNOP00000014747   ⟸   ENSRNOT00000014747
Name Modeler Protein Id AA Range Protein Structure
AF-P21451-F1-model_v2 AlphaFold P21451 1-442 view protein structure


eQTL   View at Phenogen
WGCNA   View at Phenogen
Tissue/Strain Expression   View at Phenogen

RGD ID:13699864
Promoter ID:EPDNEW_R10387
Type:single initiation site
Name:Ednrb_1
Description:endothelin receptor type B
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.01588,036,356 - 88,036,416EPDNEW


1 to 30 of 30 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-12665 BioCyc
Ensembl Genes ENSRNOG00000010997 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENSRNOT00000014747 ENTREZGENE
  ENSRNOT00000014747.6 UniProtKB/Swiss-Prot
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot
InterPro Endthln_rcpt UniProtKB/Swiss-Prot
  ETB_rcpt UniProtKB/Swiss-Prot
  GPCR_endothelin_rcpt UniProtKB/Swiss-Prot
  GPCR_Rhodpsn UniProtKB/Swiss-Prot
  GPCR_Rhodpsn_7TM UniProtKB/Swiss-Prot
KEGG Report rno:50672 UniProtKB/Swiss-Prot
NCBI Gene Ednrb ENTREZGENE
PANTHER ENDOTHELIN RECEPTOR TYPE B UniProtKB/Swiss-Prot
  G_PROTEIN_RECEP_F1_2 DOMAIN-CONTAINING PROTEIN UniProtKB/Swiss-Prot
Pfam 7tm_1 UniProtKB/Swiss-Prot
PharmGKB EDNRB RGD
PhenoGen Ednrb PhenoGen
PRINTS ENDOTHELINBR UniProtKB/Swiss-Prot
  ENDOTHELINR UniProtKB/Swiss-Prot
  GPCRRHODOPSN UniProtKB/Swiss-Prot
PROSITE G_PROTEIN_RECEP_F1_1 UniProtKB/Swiss-Prot
  G_PROTEIN_RECEP_F1_2 UniProtKB/Swiss-Prot
RatGTEx ENSRNOG00000010997 RatGTEx
SMART 7TM_GPCR_Srsx UniProtKB/Swiss-Prot
Superfamily-SCOP Family A G protein-coupled receptor-like UniProtKB/Swiss-Prot
UniProt A6HUA5 ENTREZGENE, UniProtKB/TrEMBL
  EDNRB_RAT UniProtKB/Swiss-Prot
  F2W8B2_RAT UniProtKB/TrEMBL
  P21451 ENTREZGENE
  Q9R1M2_RAT UniProtKB/TrEMBL
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Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2003-04-09 Ednrb  endothelin receptor type B      Symbol and Name updated 629477 APPROVED
2003-03-19 Ednrb  endothelin receptor type B  Etb  endothelin receptor  Data merged from RGD:621128 628472 PROVISIONAL
2002-08-07 Etb  endothelin receptor      Symbol and Name status set to provisional 70820 PROVISIONAL
2002-06-10 Ednrb  endothelin receptor type B      Symbol and Name status set to approved 70586 APPROVED

Note Type Note Reference
gene_disease mutation of this gene in humans a leads to congental aganglionic megacolon or Hirschsprung disease, participates in deoxycorticosterone acetate (DOCA)-salt-induced hypertension, cardiovascular hypertrophy and renal damage 628459
gene_disease mutation of this gene in humans a leads to congental aganglionic megacolon or Hirschsprung disease, participates in deoxycorticosterone acetate (DOCA)-salt-induced hypertension, cardiovascular hypertrophy and renal damage 628515
gene_disease mutation of this gene in humans a leads to congental aganglionic megacolon or Hirschsprung disease, participates in deoxycorticosterone acetate (DOCA)-salt-induced hypertension, cardiovascular hypertrophy and renal damage 628516
gene_expression expressed in vascular and nonvascular tissues of the lung, brain and gut, mRNA first detected in the neural crest cells and in the wall of the forgut diverticulum. 628459
gene_expression expressed in vascular and nonvascular tissues of the lung, brain and gut, mRNA first detected in the neural crest cells and in the wall of the forgut diverticulum. 628515
gene_expression expressed in vascular and nonvascular tissues of the lung, brain and gut, mRNA first detected in the neural crest cells and in the wall of the forgut diverticulum. 628516
gene_expression not expressed in spontaneously hypertensive rat hearts but was expressed in salt-hypertensive sensitive and resistant rats fed a high-salt diet 1358986
gene_function induces inositol phosphate accumulation and calcium flux 61059
gene_mutations_overexpression deletion in this gene stops the receptor expression hence elevates endothelin 1 628459
gene_mutations_overexpression deletion in this gene stops the receptor expression hence elevates endothelin 1 628515
gene_mutations_overexpression deletion in this gene stops the receptor expression hence elevates endothelin 1 628516
gene_process involved in the development of two neural crest derived cells, epidermal melanocytes and entric neurons 628459
gene_process involved in the development of two neural crest derived cells, epidermal melanocytes and entric neurons 628515
gene_process involved in the development of two neural crest derived cells, epidermal melanocytes and entric neurons 628516
gene_process may be involved in congenital aganglionic megacolon and pigmentation abnormalities 628459
gene_process may be involved in congenital aganglionic megacolon and pigmentation abnormalities 628515
gene_process may be involved in congenital aganglionic megacolon and pigmentation abnormalities 628516