Eng (endoglin) - Rat Genome Database

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Gene: Eng (endoglin) Rattus norvegicus
Analyze
Symbol: Eng
Name: endoglin
RGD ID: 1593188
Description: Enables type II transforming growth factor beta receptor binding activity. Involved in several processes, including cellular response to mechanical stimulus; extracellular matrix constituent secretion; and positive regulation of metabolic process. Located in cell surface and extracellular space. Used to study congestive heart failure; pre-eclampsia; and renal fibrosis. Biomarker of cholestasis; congestive heart failure; hepatocellular carcinoma; hypertension (multiple); and renal fibrosis. Human ortholog(s) of this gene implicated in arteriovenous malformation; arteriovenous malformations of the brain; breast cancer; hereditary hemorrhagic telangiectasia; and intracranial aneurysm. Orthologous to human ENG (endoglin); PARTICIPATES IN hypoxia inducible factor pathway; INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 3-chloropropane-1,2-diol; 4-amino-2,6-dinitrotoluene.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: MGC124909
RGD Orthologs
Human
Mouse
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8336,332,190 - 36,370,324 (+)NCBIGRCr8
mRatBN7.2315,934,566 - 15,972,618 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl315,934,518 - 15,973,230 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx319,003,353 - 19,041,237 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0327,588,363 - 27,626,245 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0325,839,360 - 25,877,319 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0311,679,530 - 11,717,486 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl311,679,530 - 11,717,485 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0317,021,673 - 17,058,548 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera310,675,660 - 10,713,537 (+)NCBICelera
Cytogenetic Map3p11NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Object Symbol
Species
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Qualifier
Evidence
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Reference
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Source
Original Reference(s)
EngRatacute lymphoblastic leukemia disease_progressionISOENG (Homo sapiens)11041565 RGD 
EngRatarteriovenous malformation susceptibilityISOENG (Homo sapiens)11041184associated with Telangiectasia and Hereditary HemorrhagicRGD 
EngRatarteriovenous malformation  ISOEng (Mus musculus)11041564 RGD 
EngRatarteriovenous malformations of the brain disease_progressionISOENG (Homo sapiens)11041171DNA:polymorphism: : 207G>A(human)RGD 
EngRatarteriovenous malformations of the brain  ISOEng (Mus musculus)11041564 RGD 
EngRatbreast cancer treatmentISOENG (Homo sapiens)7248784human tumor in mouse modelRGD 
EngRatBreast Neoplasms treatmentISOEng (Mus musculus)7257526 RGD 
EngRatChemical and Drug Induced Liver Injury  IEP 7257529protein:increased expression:liver (rat)RGD 
EngRatcholestasis  IEP 7257529protein:increased expression:liver (rat)RGD 
EngRatclear cell renal cell carcinoma severityISOENG (Homo sapiens)7248775protein:increased expression:tumor and vasculature (human)RGD 
EngRatclear cell renal cell carcinoma severityISOENG (Homo sapiens)7248780protein:decreased expression:kidney and tumor (human)RGD 
EngRatcongestive heart failure  IEP 7257540protein:increased expression:heart left ventricle (rat)RGD 
EngRatcongestive heart failure treatmentIDA 7257540 RGD 
EngRatcoronary artery disease severityISOENG (Homo sapiens)7248776protein:increased expression:plasma (human)RGD 
EngRatDiabetic Nephropathies  ISOENG (Homo sapiens)2313795associated with Diabetes Mellitus more ...RGD 
EngRatdiabetic retinopathy  ISOENG (Homo sapiens)1580961associated with Diabetes Mellitus more ...RGD 
EngRatEpistaxis  ISOEng (Mus musculus)11041563 RGD 
EngRatExperimental Radiation Injuries  ISOEng (Mus musculus)7248771kidneyRGD 
EngRatExperimental Radiation Injuries  IEP 7257525protein:decreased expression:lung (rat)RGD 
EngRathepatocellular carcinoma  IEP 7257538protein:increased expression:liver (rat)RGD 
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1 to 20 of 24 rows
Object Symbol
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Qualifier
Evidence
With
Reference
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Source
Original Reference(s)
EngRatarteriovenous malformations of the brain  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Cerebral arteriovenous malformationClinVarPMID:15879500 more ...
EngRatcongenital disorder of glycosylation Iu  ISOENG (Homo sapiens)8554872ClinVar more ...ClinVarPMID:23109149 and PMID:28492532
EngRatdevelopmental and epileptic encephalopathy  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Developmental and epileptic encephalopathyClinVarPMID:18469812 more ...
EngRatdevelopmental and epileptic encephalopathy 31A  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Epileptic encephalopathy more ...ClinVarPMID:18469812 more ...
EngRatdystonia  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Dystonic disorderClinVarPMID:28492532
EngRatearly infantile epileptic encephalopathy  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Early infantile epileptic encephalopathyClinVarPMID:18469812 more ...
EngRatGalloway-Mowat syndrome 1  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Galloway-Mowat syndrome 1ClinVarPMID:12673790 more ...
EngRatGNE myopathy  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Inclusion body myopathy quadriceps sparingClinVarPMID:15266205 more ...
EngRathereditary hemorrhagic telangiectasia  ISOENG (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10545596 more ...
EngRathereditary hemorrhagic telangiectasia  ISOENG (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10545596 more ...
EngRathereditary hemorrhagic telangiectasia  ISOENG (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10545596 more ...
EngRathereditary hemorrhagic telangiectasia  ISOENG (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10545596 more ...
EngRathereditary hemorrhagic telangiectasia  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Hereditary hemorrhagic telangiectasiaClinVarPMID:10545596 more ...
EngRatHereditary Hemorrhagic Telangiectasia, Type 1  ISOENG (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10545596 more ...
EngRatHereditary Hemorrhagic Telangiectasia, Type 2  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Oral cavity telangiectasiaClinVarPMID:25741868
EngRatjuvenile polyposis syndrome  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Juvenile PolyposisClinVarPMID:28492532
EngRatLeber congenital amaurosis  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Leber congenital amaurosisClinVarPMID:25741868 more ...
EngRatLeber congenital amaurosis  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Leber congenital amaurosisClinVarPMID:25741868 more ...
EngRatMoyamoya Disease 2  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Moyamoya disease 2ClinVarPMID:25741868
EngRatprimary coenzyme Q10 deficiency 7  ISOENG (Homo sapiens)8554872ClinVar Annotator: match by term: Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndromeClinVarPMID:22368301 more ...
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Object Symbol
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Original Reference(s)
EngRatcystic fibrosis  ISOENG (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:30806029
EngRathereditary hemorrhagic telangiectasia  ISOENG (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:15115879 and PMID:20135064
Object Symbol
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Term
Qualifier
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Reference
Notes
Source
Original Reference(s)
EngRatarteriovenous malformations of the brain  ISSEng (Mus musculus)13592920OMIM:108010MouseDO 
EngRathereditary hemorrhagic telangiectasia  ISSEng (Mus musculus)13592920OMIM:187300 more ...MouseDO 
Object Symbol
Species
Term
Qualifier
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Reference
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Original Reference(s)
EngRatHereditary Hemorrhagic Telangiectasia, Type 1  ISOENG (Homo sapiens)7240710 OMIM 

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Original Reference(s)
EngRat(+)-catechin multiple interactionsISOENG (Homo sapiens)6480464[Catechin co-treated with Grape Seed Proanthocyanidins] results in increased expression of ENG mRNACTDPMID:24763279
EngRat(1->4)-beta-D-glucan multiple interactionsISOEng (Mus musculus)6480464[perfluorooctane sulfonic acid co-treated with Cellulose] results in increased expression of ENG mRNACTDPMID:36331819
EngRat(S)-nicotine decreases expressionISOEng (Mus musculus)6480464Nicotine results in decreased expression of ENG mRNACTDPMID:17456735
EngRat1,1-dichloroethene decreases expressionISOEng (Mus musculus)6480464vinylidene chloride results in decreased expression of ENG mRNACTDPMID:26682919
EngRat1,2-dimethylhydrazine increases expressionISOEng (Mus musculus)64804641 and 2-Dimethylhydrazine results in increased expression of ENG mRNACTDPMID:22206623
EngRat17beta-estradiol affects expressionISOEng (Mus musculus)6480464Estradiol affects the expression of ENG mRNACTDPMID:15598610
EngRat17beta-estradiol decreases expressionISOEng (Mus musculus)6480464Estradiol results in decreased expression of ENG mRNACTDPMID:39298647
EngRat17beta-estradiol multiple interactionsISOENG (Homo sapiens)6480464[Estradiol co-treated with TGFB1 protein] results in increased expression of ENG mRNACTDPMID:30165855
EngRat2,3,7,8-tetrachlorodibenzodioxine affects expressionISOEng (Mus musculus)6480464Tetrachlorodibenzodioxin affects the expression of ENG mRNACTDPMID:21570461
EngRat2,3,7,8-tetrachlorodibenzodioxine affects expressionEXP 6480464Tetrachlorodibenzodioxin affects the expression of ENG mRNACTDPMID:34747641
EngRat2,3,7,8-tetrachlorodibenzodioxine increases expressionEXP 6480464Tetrachlorodibenzodioxin results in increased expression of ENG mRNACTDPMID:24475139 and PMID:32109520
EngRat2,3,7,8-tetrachlorodibenzodioxine decreases expressionISOEng (Mus musculus)6480464Tetrachlorodibenzodioxin results in decreased expression of ENG mRNACTDPMID:26290441
EngRat2-bromohexadecanoic acid multiple interactionsISOENG (Homo sapiens)64804642-bromopalmitate inhibits the reaction [[Cadmium Chloride results in increased abundance of Cadmium] which results in increased palmitoylation of ENG protein]CTDPMID:38195004
EngRat3-chloropropane-1,2-diol increases expressionEXP 6480464alpha-Chlorohydrin results in increased expression of ENG proteinCTDPMID:34915118
EngRat4,4'-sulfonyldiphenol increases expressionISOEng (Mus musculus)6480464bisphenol S results in increased expression of ENG mRNACTDPMID:30951980
EngRat4,4'-sulfonyldiphenol decreases methylationISOENG (Homo sapiens)6480464bisphenol S results in decreased methylation of ENG geneCTDPMID:31601247
EngRat4,4'-sulfonyldiphenol affects methylationISOEng (Mus musculus)6480464bisphenol S affects the methylation of ENG exonCTDPMID:33297965
EngRat4,4'-sulfonyldiphenol decreases expressionISOEng (Mus musculus)6480464bisphenol S results in decreased expression of ENG mRNACTDPMID:39298647
EngRat4-amino-2,6-dinitrotoluene affects expressionEXP 64804644-amino-2 and 6-dinitrotoluene affects the expression of ENG mRNACTDPMID:21346803
EngRat4-aminobenzhydrazide multiple interactionsISOENG (Homo sapiens)64804644-aminobenzhydrazide inhibits the reaction [hydroxyhydroquinone results in decreased expression of ENG mRNA]CTDPMID:24530881

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Biological Process
1 to 20 of 66 rows

  
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Original Reference(s)
EngRatangiogenesis acts_upstream_of_or_withinISOEng (Mus musculus)1624291MGI:2177822 more ...RGDPMID:10625534 and PMID:12941632
EngRatartery morphogenesis involved_inISOEng (Mus musculus)1624291 PMID:10348742RGDPMID:10348742
EngRatatrial cardiac muscle tissue morphogenesis involved_inISOEng (Mus musculus)1624291 PMID:17628518RGDPMID:17628518
EngRatatrioventricular canal morphogenesis involved_inISOEng (Mus musculus)1624291 PMID:19703439RGDPMID:19703439
EngRatbone development  IEP 7257537humerusRGD 
EngRatbranching involved in blood vessel morphogenesis involved_inISOEng (Mus musculus)1624291 PMID:10348742RGDPMID:10348742
EngRatcardiac atrium morphogenesis involved_inISOEng (Mus musculus)1624291 PMID:19703439RGDPMID:19703439
EngRatcardiac jelly development NOT|involved_inISOEng (Mus musculus)1624291 PMID:19703439RGDPMID:19703439
EngRatcardiac ventricle morphogenesis involved_inISOEng (Mus musculus)1624291 PMID:19703439RGDPMID:19703439
EngRatcell chemotaxis involved_inISOENG (Homo sapiens) and UniProtKB:P17813-11624291 PMID:18223685RGDPMID:18223685
EngRatcell migration involved_inISOENG (Homo sapiens) and UniProtKB:P17813-11624291 PMID:18223685RGDPMID:18223685
EngRatcell migration involved in endocardial cushion formation acts_upstream_of_or_withinISOEng (Mus musculus)1624291MGI:2177824 PMID:19703439RGDPMID:19703439
EngRatcell motility involved_inISOENG (Homo sapiens) and UniProtKB:P17813-11624291 PMID:18223685RGDPMID:18223685
EngRatcellular response to mechanical stimulus  IEP 7248789mechanical stretchRGD 
EngRatcentral nervous system vasculogenesis involved_inISOENG (Homo sapiens)1624291 PMID:7894484RGDPMID:7894484
EngRatdetection of hypoxia involved_inISOENG (Homo sapiens) more ...1624291 PMID:18156205RGDPMID:18156205
EngRatdorsal aorta morphogenesis involved_inISOEng (Mus musculus)1624291 PMID:12941632RGDPMID:12941632
EngRatendocardial cushion morphogenesis involved_inISOEng (Mus musculus)1624291 PMID:12941632 and PMID:19703439RGDPMID:12941632 and PMID:19703439
EngRatendocardial cushion to mesenchymal transition NOT|involved_inISOEng (Mus musculus)1624291 PMID:12941632RGDPMID:12941632
EngRatepithelial to mesenchymal transition involved in endocardial cushion formation involved_inISOEng (Mus musculus)1624291 PMID:19703439RGDPMID:19703439
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Cellular Component
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Molecular Function
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Original Reference(s)
EngRatBMP binding contributes_toISOENG (Homo sapiens)1624291UniProtKB:P18075 and PMID:9872992RGDPMID:9872992
EngRatcoreceptor activity enablesISOENG (Homo sapiens) and UniProtKB:P17813-11624291 PMID:18223685RGDPMID:18223685
EngRatcoreceptor activity enablesISOENG (Homo sapiens)1624291UniProtKB:P36897 and PMID:12015308RGDPMID:12015308
EngRatgalactose binding enablesISOENG (Homo sapiens)1624291 PMID:3262645RGDPMID:3262645
EngRatglycosaminoglycan binding enablesISOENG (Homo sapiens)1624291 PMID:3262645RGDPMID:3262645
EngRatglycosaminoglycan binding enablesISOENG (Sus scrofa)1624291 PMID:8294451RGDPMID:8294451
EngRatidentical protein binding enablesISOENG (Homo sapiens)1624291UniProtKB:P17813 and PMID:28564608RGDPMID:28564608
EngRatprotein binding enablesISOENG (Homo sapiens)1624291UniProtKB:P01137 more ...RGDPMID:15702480 more ...
EngRatprotein binding enablesISOEng (Mus musculus)1624291MGI:1924155 PMID:23868260RGDPMID:23868260
EngRatprotein binding enablesISOENG (Homo sapiens) and UniProtKB:P17813-11624291UniProtKB:P02750 and PMID:23868260RGDPMID:23868260
EngRatprotein homodimerization activity enablesISOEng (Mus musculus)1624291UniProtKB:Q63961 and PMID:8194490RGDPMID:8194490
EngRatprotein homodimerization activity enablesISOENG (Homo sapiens) and UniProtKB:P17813-21624291UniProtKB:P17813-2 and PMID:8370410RGDPMID:8370410
EngRatsignaling receptor activator activity enablesISOENG (Homo sapiens)1624291 PMID:12015308RGDPMID:12015308
EngRattransforming growth factor beta binding contributes_toISOENG (Homo sapiens)1624291UniProtKB:P07200 more ...RGDPMID:9872992
EngRattransforming growth factor beta binding enablesISOEng (Mus musculus)1624291 PMID:8194490RGDPMID:8194490
EngRattransforming growth factor beta binding enablesISOENG (Homo sapiens) more ...1624291UniProtKB:P01137 and PMID:8370410RGDPMID:8370410
EngRattransforming growth factor beta binding enablesISOENG (Homo sapiens)1624291UniProtKB:P01137 more ...RGDPMID:1326540
EngRattransforming growth factor beta receptor activity  NAS 1601032 RGD 
EngRattype I transforming growth factor beta receptor binding enablesISOENG (Sus scrofa)1624291 PMID:8294451RGDPMID:8294451
EngRattype I transforming growth factor beta receptor binding enablesISOENG (Homo sapiens) more ...1624291UniProtKB:P36897 and PMID:18974388RGDPMID:18974388
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Imported Annotations - PID (archival)

Object Symbol
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Reference
Notes
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Original Reference(s)
EngRathypoxia inducible factor pathway   ISOENG (Homo sapiens)6484113 PIDPID:200202

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#
Reference Title
Reference Citation
1. Cellular basis of diabetic nephropathy: V. Endoglin expression levels and diabetic nephropathy risk in patients with Type 1 diabetes. Alvarez-Munoz P, etal., J Diabetes Complications. 2009 Apr 21.
2. Clinical heterogeneity in hereditary haemorrhagic telangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin? Berg JN, etal., J Med Genet. 1996 Mar;33(3):256-7.
3. Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype. Bossler AD, etal., Hum Mutat. 2006 Jul;27(7):667-75.
4. A murine model of hereditary hemorrhagic telangiectasia. Bourdeau A, etal., J Clin Invest. 1999 Nov;104(10):1343-51.
5. Gene expression profiles that segregate patients with childhood acute lymphoblastic leukaemia: an independent validation study identifies that endoglin associates with patient outcome. Catchpoole D, etal., Leuk Res. 2007 Dec;31(12):1741-7. Epub 2007 Jun 18.
6. Transforming growth factor beta receptor endoglin is expressed in cardiac fibroblasts and modulates profibrogenic actions of angiotensin II. Chen K, etal., Circ Res. 2004 Dec 10;95(12):1167-73. Epub 2004 Nov 11.
7. Novel brain arteriovenous malformation mouse models for type 1 hereditary hemorrhagic telangiectasia. Choi EJ, etal., PLoS One. 2014 Feb 10;9(2):e88511. doi: 10.1371/journal.pone.0088511. eCollection 2014.
8. Endoglin regulates renal ischaemia-reperfusion injury. Docherty NG, etal., Nephrol Dial Transplant. 2006 Aug;21(8):2106-19. Epub 2006 Jun 4.
9. Preeclampsia-like symptoms induced in mice by fetoplacental expression of STOX1 are reversed by aspirin treatment. Doridot L, etal., Hypertension. 2013 Mar;61(3):662-8. doi: 10.1161/HYPERTENSIONAHA.111.202994. Epub 2013 Jan 28.
10. Assessment of the prognostic significance of endoglin (CD105) in clear cell renal cell carcinoma using automated image analysis. Dubinski W, etal., Hum Pathol. 2012 Jul;43(7):1037-43. doi: 10.1016/j.humpath.2011.08.012. Epub 2011 Dec 26.
11. Tumour epithelial expression levels of endocannabinoid markers modulate the value of endoglin-positive vascular density as a prognostic marker in prostate cancer. Fowler CJ, etal., Biochim Biophys Acta. 2012 Dec 20. pii: S1388-1981(12)00259-4. doi: 10.1016/j.bbalip.2012.12.005.
12. Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Gaudet P, etal., Brief Bioinform. 2011 Sep;12(5):449-62. doi: 10.1093/bib/bbr042. Epub 2011 Aug 27.
13. Hypertension produced by placental ischemia in pregnant rats is associated with increased soluble endoglin expression. Gilbert JS, etal., Hypertension. 2009 Feb;53(2):399-403. Epub 2008 Dec 15.
14. Long-term high salt diet causes hypertension and alters renal cytokine gene expression profiles in Sprague-Dawley rats. Gu JW, etal., Beijing Da Xue Xue Bao. 2009 Oct 18;41(5):505-15.
15. Plasma endoglin as a marker to predict cardiovascular events in patients with chronic coronary artery diseases. Ikemoto T, etal., Heart Vessels. 2012 Jul;27(4):344-51. doi: 10.1007/s00380-011-0163-z. Epub 2011 Jun 11.
16. Autoantibody-mediated angiotensin receptor activation contributes to preeclampsia through tumor necrosis factor-alpha signaling. Irani RA, etal., Hypertension. 2010 May;55(5):1246-53. doi: 10.1161/HYPERTENSIONAHA.110.150540. Epub 2010 Mar 29.
17. Magnesium sulfate therapy of preeclampsia: an old tool with new mechanism of action and prospect in management and prophylaxis. Korish AA Hypertens Res. 2012 Oct;35(10):1005-11. doi: 10.1038/hr.2012.103. Epub 2012 Jul 5.
18. Circulating angiogenic factors and urinary prolactin as predictors of adverse outcomes in women with preeclampsia. Leanos-Miranda A, etal., Hypertension. 2013 May;61(5):1118-25. doi: 10.1161/HYPERTENSIONAHA.111.00754. Epub 2013 Mar 4.
19. Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France. Lesca G, etal., Hum Mutat 2004 Apr;23(4):289-99.
20. Reduced endothelial secretion and plasma levels of transforming growth factor-beta1 in patients with hereditary hemorrhagic telangiectasia type 1. Letarte M, etal., Cardiovasc Res. 2005 Oct 1;68(1):155-64.
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PMID:1326540   PMID:1537377   PMID:3262645   PMID:8194490   PMID:8294451   PMID:8370410   PMID:9872992   PMID:10348742   PMID:10625534   PMID:12015308   PMID:12477932   PMID:12941632  
PMID:15702480   PMID:17068149   PMID:17628518   PMID:18156205   PMID:18223685   PMID:18974388   PMID:19004009   PMID:19703439   PMID:19736306   PMID:20978343   PMID:21423176   PMID:23868260  
PMID:24392114   PMID:25936493   PMID:26857067   PMID:27466499   PMID:27822781   PMID:28564608   PMID:28590142   PMID:28859090   PMID:29677638   PMID:32972452  



Eng
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8336,332,190 - 36,370,324 (+)NCBIGRCr8
mRatBN7.2315,934,566 - 15,972,618 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl315,934,518 - 15,973,230 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx319,003,353 - 19,041,237 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0327,588,363 - 27,626,245 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0325,839,360 - 25,877,319 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0311,679,530 - 11,717,486 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl311,679,530 - 11,717,485 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0317,021,673 - 17,058,548 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera310,675,660 - 10,713,537 (+)NCBICelera
Cytogenetic Map3p11NCBI
ENG
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389127,815,016 - 127,854,658 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9127,811,130 - 127,854,773 (-)EnsemblGRCh38hg38GRCh38
GRCh379130,577,295 - 130,616,937 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 369129,617,115 - 129,656,805 (-)NCBINCBI36Build 36hg18NCBI36
Build 349127,656,849 - 127,696,538NCBI
Celera9101,228,133 - 101,267,888 (-)NCBICelera
Cytogenetic Map9q34.11NCBI
HuRef9100,194,111 - 100,234,515 (-)NCBIHuRef
CHM1_19130,728,823 - 130,768,983 (-)NCBICHM1_1
T2T-CHM13v2.09140,022,435 - 140,062,072 (-)NCBIT2T-CHM13v2.0
Eng
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39232,536,607 - 32,572,681 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl232,536,607 - 32,572,681 (+)EnsemblGRCm39 Ensembl
GRCm38232,646,595 - 32,682,669 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl232,646,595 - 32,682,669 (+)EnsemblGRCm38mm10GRCm38
MGSCv37232,502,115 - 32,538,189 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36232,468,604 - 32,504,127 (+)NCBIMGSCv36mm8
Celera232,353,177 - 32,389,276 (+)NCBICelera
Cytogenetic Map2BNCBI
cM Map222.09NCBI
Eng
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955419818,932 - 852,694 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955419818,797 - 853,319 (+)NCBIChiLan1.0ChiLan1.0
ENG
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21111,500,636 - 11,540,554 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1911,502,983 - 11,542,901 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0998,934,080 - 98,973,862 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.19127,605,608 - 127,644,641 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl9127,605,608 - 127,644,641 (-)Ensemblpanpan1.1panPan2
ENG
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1955,558,246 - 55,590,081 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl955,558,305 - 55,589,064 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha954,752,221 - 54,783,620 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0956,480,195 - 56,511,601 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl956,480,054 - 56,511,589 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1955,240,157 - 55,271,556 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0955,554,890 - 55,586,290 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0955,646,354 - 55,677,713 (+)NCBIUU_Cfam_GSD_1.0
Eng
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947195,698,638 - 195,730,666 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648715,467,835 - 15,477,488 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648715,467,165 - 15,499,180 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ENG
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1268,309,400 - 268,343,783 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11268,309,379 - 268,343,861 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21302,232,063 - 302,266,139 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ENG
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11210,274,705 - 10,315,715 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1210,275,064 - 10,315,040 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660795,905,669 - 5,949,288 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Eng
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247607,703,820 - 7,734,457 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247607,703,979 - 7,735,636 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in Eng
270 total Variants


Assembly: mRatBN7.2

Chromosome Start Pos End Pos Reference Nucleotide Variant Nucleotide Variant Type Strain Variant Page
3 15934883 15934884 A C snv PVG/Seac (2019), European Variation Archive Release 6, European Variation Archive Release 4, European Variation Archive Release 3 View more Information

Predicted Target Of
Summary Value
Count of predictions:646
Count of miRNA genes:183
Interacting mature miRNAs:218
Transcripts:ENSRNOT00000071801, ENSRNOT00000074562
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 25 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
1358357Srcrtb1Stress Responsive Cort Basal QTL 16.360.002blood corticosterone amount (VT:0005345)plasma corticosterone level (CMO:0001173)3865816227494778Rat
6893355Bw101Body weight QTL 1010.40.38body mass (VT:0001259)body weight (CMO:0000012)31077870430357018Rat
10401810Kidm53Kidney mass QTL 53kidney mass (VT:0002707)both kidneys wet weight to body weight ratio (CMO:0000340)3822719447233430Rat
1298526Arunc3Aerobic running capacity QTL 32.2exercise endurance trait (VT:0002332)maximum distance run on treadmill (CMO:0001406)3822719433703538Rat
8693641Alc30Alcohol consumption QTL 3020.739drinking behavior trait (VT:0001422)calculated ethanol drink intake rate (CMO:0001615)31043430624512004Rat
2298542Neuinf11Neuroinflammation QTL 113.9nervous system integrity trait (VT:0010566)spinal cord complement component 1, q subcomponent, B chain mRNA level (CMO:0002126)31500542276927699Rat
1558657Cm43Cardiac mass QTL 436.63e-08heart mass (VT:0007028)heart wet weight (CMO:0000069)31077882330356773Rat
631568Bp92Blood pressure QTL 922.20.005arterial blood pressure trait (VT:2000000)systolic blood pressure (CMO:0000004)3139874793Rat
6893363Bw105Body weight QTL 1052.60.0036body mass (VT:0001259)body weight (CMO:0000012)31077870430357018Rat
61468Bp15Blood pressure QTL 154.4blood pressure trait (VT:0000183)pulse pressure (CMO:0000292)3133278763Rat

1 to 10 of 25 rows
D3Got2  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2315,952,555 - 15,952,811 (+)MAPPERmRatBN7.2
mRatBN7.2315,952,555 - 15,952,876 (+)MAPPERmRatBN7.2
Rnor_6.0311,697,544 - 11,698,063NCBIRnor6.0
Rnor_6.0311,697,544 - 11,697,799NCBIRnor6.0
Rnor_5.0317,039,439 - 17,039,958UniSTSRnor5.0
Rnor_5.0317,039,439 - 17,039,694UniSTSRnor5.0
Celera310,693,503 - 10,693,760UniSTS
RH 3.4 Map368.4RGD
RH 3.4 Map368.4UniSTS
RH 2.0 Map30.0RGD
RH133417  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2315,972,395 - 15,972,591 (+)MAPPERmRatBN7.2
Rnor_6.0311,717,263 - 11,717,458NCBIRnor6.0
Rnor_5.0317,058,326 - 17,058,521UniSTSRnor5.0
Celera310,713,315 - 10,713,510UniSTS
RH 3.4 Map372.7UniSTS
RH134698  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2315,972,879 - 15,973,065 (+)MAPPERmRatBN7.2
Rnor_6.0311,717,747 - 11,717,932NCBIRnor6.0
Rnor_5.0317,058,810 - 17,058,995UniSTSRnor5.0
Celera310,713,799 - 10,713,984UniSTS
RH 3.4 Map370.8UniSTS




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: ENSRNOT00000071801   ⟹   ENSRNOP00000066355
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl315,934,532 - 15,972,619 (+)Ensembl
Rnor_6.0 Ensembl311,679,530 - 11,717,485 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000074562   ⟹   ENSRNOP00000066838
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl315,934,518 - 15,973,230 (+)Ensembl
Rnor_6.0 Ensembl311,679,530 - 11,717,485 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000101522   ⟹   ENSRNOP00000089152
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl315,944,396 - 15,973,230 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000114060   ⟹   ENSRNOP00000094124
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl315,942,606 - 15,973,230 (+)Ensembl
RefSeq Acc Id: NM_001010968   ⟹   NP_001010968
RefSeq Status: VALIDATED
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8336,332,279 - 36,370,323 (+)NCBI
mRatBN7.2315,934,566 - 15,972,618 (+)NCBI
Rnor_6.0311,679,530 - 11,717,485 (+)NCBI
Rnor_5.0317,021,673 - 17,058,548 (+)NCBI
Celera310,675,660 - 10,713,537 (+)RGD
Sequence:
RefSeq Acc Id: XM_063284324   ⟹   XP_063140394
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8336,332,190 - 36,370,324 (+)NCBI
1 to 10 of 10 rows
Protein RefSeqs NP_001010968 (Get FASTA)   NCBI Sequence Viewer  
  XP_063140394 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI05861 (Get FASTA)   NCBI Sequence Viewer  
  AAS67893 (Get FASTA)   NCBI Sequence Viewer  
  EDL93221 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000066355.3
  ENSRNOP00000066838
  ENSRNOP00000066838.3
  ENSRNOP00000089152.1
  ENSRNOP00000094124.1
1 to 10 of 10 rows
RefSeq Acc Id: NP_001010968   ⟸   NM_001010968
- Peptide Label: precursor
- UniProtKB: Q6Q3E8 (UniProtKB/TrEMBL),   M0RBA8 (UniProtKB/TrEMBL),   A0A9K3Y7N3 (UniProtKB/TrEMBL),   A0A8I6GL08 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSRNOP00000066355   ⟸   ENSRNOT00000071801
Ensembl Acc Id: ENSRNOP00000066838   ⟸   ENSRNOT00000074562
Ensembl Acc Id: ENSRNOP00000094124   ⟸   ENSRNOT00000114060
Ensembl Acc Id: ENSRNOP00000089152   ⟸   ENSRNOT00000101522
ZP

Name Modeler Protein Id AA Range Protein Structure
AF-M0RBA8-F1-model_v2 AlphaFold M0RBA8 1-699 view protein structure


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

RGD ID:13691990
Promoter ID:EPDNEW_R2515
Type:initiation region
Name:Eng_1
Description:endoglin
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_6.0311,679,512 - 11,679,572EPDNEW


1 to 25 of 25 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-50128 BioCyc
Ensembl Genes ENSRNOG00000050190 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENSRNOT00000071801.3 UniProtKB/TrEMBL
  ENSRNOT00000074562 ENTREZGENE
  ENSRNOT00000074562.4 UniProtKB/TrEMBL
  ENSRNOT00000101522.1 UniProtKB/TrEMBL
  ENSRNOT00000114060.1 UniProtKB/TrEMBL
IMAGE_CLONE IMAGE:7456529 IMAGE-MGC_LOAD
InterPro ZP_dom UniProtKB/TrEMBL
KEGG Report rno:497010 UniProtKB/TrEMBL
MGC_CLONE MGC:124909 IMAGE-MGC_LOAD
NCBI Gene 497010 ENTREZGENE
PANTHER ENDOGLIN UniProtKB/TrEMBL
  ENDOGLIN/TGF-BETA RECEPTOR TYPE III UniProtKB/TrEMBL
Pfam Zona_pellucida UniProtKB/TrEMBL
PhenoGen Eng PhenoGen
RatGTEx ENSRNOG00000050190 RatGTEx
UniProt A0A8I6A813_RAT UniProtKB/TrEMBL
  A0A8I6GL08 ENTREZGENE, UniProtKB/TrEMBL
  A0A9K3Y7N3 ENTREZGENE, UniProtKB/TrEMBL
  M0RA19_RAT UniProtKB/TrEMBL
  M0RBA8 ENTREZGENE
  Q3KR75 ENTREZGENE, UniProtKB/TrEMBL
  Q6Q3E8 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary M0RBA8 UniProtKB/TrEMBL
1 to 25 of 25 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2006-11-20 Eng  endoglin      Symbol and Name status set to provisional 70820 PROVISIONAL