Vwf (von Willebrand factor) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: Vwf (von Willebrand factor) Rattus norvegicus
Analyze
Symbol: Vwf
Name: von Willebrand factor
RGD ID: 621759
Description: Predicted to enable several functions, including identical protein binding activity; integrin binding activity; and protein-folding chaperone binding activity. Involved in several processes, including cellular response to cold; cellular response to lipopolysaccharide; and liver regeneration. Located in collagen-containing extracellular matrix and extracellular space. Used to study transient cerebral ischemia. Biomarker of hypertension; mesangial proliferative glomerulonephritis; myocardial infarction; pulmonary fibrosis; and type 1 diabetes mellitus. Human ortholog(s) of this gene implicated in several diseases, including Behcet's disease; Bernard-Soulier syndrome; end stage renal disease; essential thrombocythemia; and von Willebrand's disease (multiple). Orthologous to human VWF (von Willebrand factor); PARTICIPATES IN platelet aggregation pathway; cell-extracellular matrix signaling pathway; coagulation cascade pathway; INTERACTS WITH 17alpha-ethynylestradiol; 2,3,7,8-tetrachlorodibenzodioxine; 6-propyl-2-thiouracil.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: von Willebrand factor homolog
RGD Orthologs
Human
Mouse
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: Vwfem2Mcwi   Vwfem3Mcwi   Vwfem1Mcwi   Vwfem4Mcwi  
Genetic Models: SS-Vwfem2Mcwi-/- SD-Vwfem1Mcwi-/- SS-Vwfem3Mcwi-/- SS-Vwfem4Mcwi
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr84160,042,900 - 160,177,757 (+)NCBIGRCr8
mRatBN7.24158,360,152 - 158,491,539 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl4158,360,152 - 158,491,539 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx4164,595,998 - 164,727,404 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.04160,378,929 - 160,510,343 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.04159,012,985 - 159,144,157 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.04158,085,059 - 158,219,525 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl4158,088,505 - 158,219,523 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04225,098,521 - 225,229,257 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44161,723,415 - 161,854,766 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.14162,053,065 - 162,055,090 (+)NCBI
Celera4147,092,791 - 147,223,711 (+)NCBICelera
Cytogenetic Map4q42NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


1 to 20 of 61 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatAcute Experimental Pancreatitis  IEP 11079229protein:increased expression:plasma:RGD 
VwfRatAortic Injuries  IEP 11079230protein:increased expression:endothelial cell:RGD 
VwfRatatrial fibrillation treatmentISOVWF (Homo sapiens)7205648 RGD 
VwfRatBehcet's disease  ISOVWF (Homo sapiens)1580642 RGD 
VwfRatBernard-Soulier syndrome  ISOVWF (Homo sapiens)1580643 RGD 
VwfRatbipolar disorder  ISOVWF (Homo sapiens)7207027protein:increased expression:plasmaRGD 
VwfRatcarotid artery disease  ISOVWF (Homo sapiens)7207026associated with Kidney Failure and ChronicRGD 
VwfRatChemical and Drug Induced Liver Injury  IEP 11079232protein:increased expression:liver:RGD 
VwfRatCoronary Disease  ISOVWF (Homo sapiens)1580647 RGD 
VwfRatCytomegalovirus Infections  ISOVWF (Homo sapiens)38508895protein:increased expression:plasma (human)RGD 
VwfRatdiabetes mellitus treatmentISOVwf (Mus musculus)7207029 RGD 
VwfRatDiabetic Nephropathies  ISOVWF (Homo sapiens)401851916mRNA:increased expression:nephron tubule (human)RGD 
VwfRatdiabetic retinopathy  ISOVWF (Homo sapiens)1580648 RGD 
VwfRatend stage renal disease  ISOVWF (Homo sapiens)7205646protein:increased oxidation:plasmaRGD 
VwfRatend stage renal disease treatmentISOVWF (Homo sapiens)7205649 RGD 
VwfRatend stage renal disease disease_progressionISOVWF (Homo sapiens)7205641 RGD 
VwfRatEndotoxemia  IEP 11079230protein:increased expression:endothelial cell:RGD 
VwfRatessential thrombocythemia  ISOVWF (Homo sapiens)11073823 RGD 
VwfRatExperimental Diabetes Mellitus  IEP 1625712protein:increased expression:plasmaRGD 
VwfRatExperimental Liver Cirrhosis  IEP 11079232protein:increased expression:liver:RGD 
1 to 20 of 61 rows
1 to 20 of 20 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatautosomal hemophilia A  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: AUTOSOMAL HEMOPHILIA AClinVarPMID:25741868
VwfRatblood coagulation disease  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: Abnormality of coagulationClinVarPMID:11686103 more ...
VwfRatepisodic ataxia type 1  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: Episodic ataxia type 1ClinVarPMID:28492532
VwfRatfactor VIII deficiency  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: Factor 8 deficiency and congenitalClinVarPMID:25741868
VwfRatgenetic disease  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:11159522 more ...
VwfRatHemorrhage  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: HemorrhageClinVarPMID:16985174 more ...
VwfRathemorrhagic disease  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: Abnormal bleedingClinVarPMID:10494764 more ...
VwfRatHyperphosphatemic Familial Tumoral Calcinosis 1  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: Tumoral calcinosis more ...ClinVarPMID:25378588 and PMID:29389098
VwfRatlymphoproliferative syndrome 2  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: Lymphoproliferative syndrome 2ClinVarPMID:28492532
VwfRatperiventricular nodular heterotopia  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: Heterotopia more ...ClinVarPMID:25741868
VwfRatthrombocytopenia  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: ThrombocytopeniaClinVarPMID:11122100 more ...
VwfRatthrombosis  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: ThrombusClinVarPMID:12649144 more ...
VwfRatVon Willebrand Factor, Deficiency  ISOVWF (Homo sapiens)8554872ClinVar Annotator: match by term: Reduced von Willebrand factor activityClinVarPMID:10669167 more ...
VwfRatvon Willebrand's disease  ISOVWF (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10233434 more ...
VwfRatvon Willebrand's disease  ISOVWF (Homo sapiens)8554872ClinVar more ...ClinVarPMID:28581694 more ...
VwfRatvon Willebrand's disease 1  ISOVWF (Homo sapiens)8554872ClinVar more ...ClinVarPMID:33527515 more ...
VwfRatvon Willebrand's disease 1  ISOVWF (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10669167 more ...
VwfRatvon Willebrand's disease 2  ISOVWF (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10233434 more ...
VwfRatvon Willebrand's disease 2  ISOVWF (Homo sapiens)8554872ClinVar more ...ClinVarPMID:29115006 more ...
VwfRatvon Willebrand's disease 3  ISOVWF (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10959712 more ...
1 to 20 of 20 rows
1 to 15 of 15 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatatrial fibrillation  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:17890461
VwfRatautism spectrum disorder  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:35663546
VwfRatcardiovascular system disease  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:16332659
VwfRatChemical and Drug Induced Liver Injury  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:28527913
VwfRatcongestive heart failure  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:22352330
VwfRatDrug Hypersensitivity Syndrome  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:34142820
VwfRatexanthem  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:34142820
VwfRatExperimental Liver Cirrhosis  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:28527913
VwfRathypertension  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:12149661 more ...
VwfRatintracranial thrombosis  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:3111251
VwfRatStevens-Johnson syndrome  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:34142820
VwfRatthrombosis  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:3875694 and PMID:22352330
VwfRatvon Willebrand's disease 1  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
VwfRatvon Willebrand's disease 2  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
VwfRatvon Willebrand's disease 3  ISOVWF (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
1 to 15 of 15 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatStroke  ISOVWF (Homo sapiens)1331525 GAD 
VwfRatvon Willebrand's disease  ISOVWF (Homo sapiens)1331525 GAD 
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatvon Willebrand's disease  ISSVwf (Mus musculus)13592920 MouseDO 
VwfRatvon Willebrand's disease 2  ISSVwf (Mus musculus)13592920OMIM:613554MouseDO 
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatvon Willebrand's disease 1  ISOVWF (Homo sapiens)7240710 OMIM 
VwfRatvon Willebrand's disease 2  ISOVWF (Homo sapiens)7240710 OMIM 
VwfRatvon Willebrand's disease 3  ISOVWF (Homo sapiens)7240710 OMIM 

1 to 20 of 203 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRat(+)-dexrazoxane multiple interactionsISOVwf (Mus musculus)6480464[Dexrazoxane co-treated with Doxorubicin] results in increased expression of VWF protein and Dexrazoxane inhibits the reaction [Doxorubicin results in increased expression of VWF protein]CTDPMID:30517846
VwfRat(S)-nicotine decreases expressionISOVwf (Mus musculus)6480464Nicotine results in decreased expression of VWF mRNACTDPMID:17456735
VwfRat(S)-nicotine increases expressionISOVWF (Homo sapiens)6480464Nicotine results in increased expression of VWF mRNACTDPMID:11166759
VwfRat1,1-bis(2-aminoethyl)-2-hydroxy-3-oxotriazane multiple interactionsISOVWF (Homo sapiens)64804642 and 2'-(hydroxynitrosohydrazono)bis-ethanamine inhibits the reaction [TNF protein results in increased secretion of VWF protein]CTDPMID:34678311
VwfRat1,2-dimethylhydrazine increases expressionISOVwf (Mus musculus)64804641 and 2-Dimethylhydrazine results in increased expression of VWF mRNACTDPMID:22206623
VwfRat1-naphthyl isothiocyanate multiple interactionsISOVwf (Mus musculus)64804641-Naphthylisothiocyanate results in increased expression of and results in increased activity of VWF protein more ...CTDPMID:34619301
VwfRat1-naphthyl isothiocyanate affects response to substanceISOVwf (Mus musculus)6480464VWF protein affects the susceptibility to 1-NaphthylisothiocyanateCTDPMID:34619301
VwfRat17alpha-ethynylestradiol multiple interactionsISOVWF (Homo sapiens)6480464[Ethinyl Estradiol co-treated with Gestodene] results in increased expression of VWF proteinCTDPMID:12616983
VwfRat17alpha-ethynylestradiol increases expressionEXP 6480464Ethinyl Estradiol results in increased expression of VWF mRNACTDPMID:29097150
VwfRat17alpha-ethynylestradiol affects expressionISOVwf (Mus musculus)6480464Ethinyl Estradiol affects the expression of VWF mRNACTDPMID:17555576
VwfRat17alpha-ethynylestradiol decreases expressionISOVWF (Homo sapiens)6480464Ethinyl Estradiol results in decreased expression of VWF mRNA and Ethinyl Estradiol results in decreased expression of VWF proteinCTDPMID:18298783 and PMID:18936297
VwfRat17beta-estradiol multiple interactionsISOVWF (Homo sapiens)6480464[Estradiol co-treated with TGFB1 protein] results in decreased expression of VWF mRNA and [Progesterone co-treated with Estradiol] results in increased expression of VWF mRNACTDPMID:18692832 and PMID:30165855
VwfRat17beta-estradiol increases expressionISOVWF (Homo sapiens)6480464Estradiol results in increased expression of VWF mRNACTDPMID:31614463
VwfRat2,3,7,8-tetrachlorodibenzodioxine affects expressionEXP 6480464Tetrachlorodibenzodioxin affects the expression of VWF mRNACTDPMID:22298810
VwfRat2,3,7,8-tetrachlorodibenzodioxine decreases expressionEXP 6480464Tetrachlorodibenzodioxin results in decreased expression of VWF mRNACTDPMID:34747641
VwfRat2,4,6-tribromophenol increases expressionISOVWF (Homo sapiens)64804642 more ...CTDPMID:31675489
VwfRat2,4,6-trinitrobenzenesulfonic acid increases expressionISOVwf (Mus musculus)6480464Trinitrobenzenesulfonic Acid results in increased expression of VWF proteinCTDPMID:25307345
VwfRat2,4,6-trinitrobenzenesulfonic acid multiple interactionsISOVwf (Mus musculus)6480464NTS protein promotes the reaction [Trinitrobenzenesulfonic Acid results in increased expression of VWF protein]CTDPMID:25307345
VwfRat2,4-dibromophenyl 2,4,5-tribromophenyl ether affects expressionISOVwf (Mus musculus)64804642 more ...CTDPMID:38648751
VwfRat2-hydroxypropanoic acid decreases expressionISOVWF (Homo sapiens)6480464Lactic Acid results in decreased expression of VWF mRNACTDPMID:30851411

1 to 20 of 203 rows

Biological Process
1 to 20 of 36 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatactivation of blood coagulation via clotting cascade acts_upstream_of_or_withinISOVwf (Mus musculus)1624291 PMID:30573509RGDPMID:30573509
VwfRatblood coagulation involved_inIEAUniProtKB-KW:KW-00941600115GO_REF:0000043UniProtGO_REF:0000043
VwfRatblood coagulation involved_inIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatblood coagulation acts_upstream_of_or_withinISOVwf (Mus musculus)1624291MGI:2153009 PMID:17380206 more ...RGDPMID:17380206 more ...
VwfRatblood coagulation involved_inIEAUniRule:UR0015287711600115GO_REF:0000104UniProtGO_REF:0000104
VwfRatblood coagulation involved_inISOVWF (Homo sapiens)1624291 PMID:16409464RGDPMID:16409464
VwfRatcell adhesion involved_inISOVWF (Homo sapiens)1624291 PMID:10764791RGDPMID:10764791
VwfRatcell adhesion involved_inIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatcell adhesion involved_inIEAUniRule:UR0015287711600115GO_REF:0000104UniProtGO_REF:0000104
VwfRatcell adhesion involved_inIEAUniProtKB-KW:KW-01301600115GO_REF:0000043UniProtGO_REF:0000043
VwfRatcell-substrate adhesion involved_inISOVWF (Homo sapiens)1624291 PMID:9079671RGDPMID:9079671
VwfRatcell-substrate adhesion involved_inIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatcell-substrate adhesion acts_upstream_of_or_withinISOVwf (Mus musculus)1624291MGI:2153009 PMID:11071623RGDPMID:11071623
VwfRatcell-substrate adhesion involved_inIEAUniRule:UR0015287711600115GO_REF:0000104UniProtGO_REF:0000104
VwfRatcellular response to cold  IEP 11079231 RGD 
VwfRatcellular response to lipopolysaccharide  IEP 11079229 RGD 
VwfRatextracellular matrix organization involved_inIBAMGI:1915803 and PANTHER:PTN0027314141600115GO_REF:0000033GO_CentralGO_REF:0000033
VwfRathemostasis involved_inISOVWF (Homo sapiens)1624291 PMID:10887119RGDPMID:10887119
VwfRathemostasis involved_inIEAUniRule:UR0015287711600115GO_REF:0000104UniProtGO_REF:0000104
VwfRathemostasis acts_upstream_of_or_withinISOVwf (Mus musculus)1624291MGI:2153009 PMID:9689113RGDPMID:9689113
1 to 20 of 36 rows

Cellular Component
1 to 17 of 17 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatcollagen-containing extracellular matrix  IDA 1599021 RGD 
VwfRatcollagen-containing extracellular matrix is_active_inIBAPANTHER:PTN002731414 and Vwf (Rattus norvegicus)1600115GO_REF:0000033GO_CentralGO_REF:0000033
VwfRatcollagen-containing extracellular matrix located_inISOVWF (Homo sapiens)1624291 PMID:6754744RGDPMID:6754744
VwfRatendoplasmic reticulum located_inIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatendoplasmic reticulum located_inISOVWF (Homo sapiens)1624291 PMID:6754744RGDPMID:6754744
VwfRatexternal side of plasma membrane located_inISOVwf (Mus musculus)1624291 PMID:8562500RGDPMID:8562500
VwfRatextracellular region located_inIEAUniProtKB-KW:KW-09641600115GO_REF:0000043UniProtGO_REF:0000043
VwfRatextracellular region located_inIEAUniRule:UR0015287711600115GO_REF:0000104UniProtGO_REF:0000104
VwfRatextracellular region located_inIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatextracellular region located_inISOVWF (Homo sapiens)1624291 PMID:10887119RGDPMID:10887119
VwfRatextracellular region located_inIEAUniProtKB-SubCell:SL-02431600115GO_REF:0000044UniProtGO_REF:0000044
VwfRatextracellular space  IDA 727737 RGD 
VwfRatextracellular space located_inISOVwf (Mus musculus)1624291 PMID:30573509RGDPMID:30573509
VwfRatWeibel-Palade body located_inISOVWF (Homo sapiens)1624291 PMID:3082891 and PMID:3087627RGDPMID:3082891 and PMID:3087627
VwfRatWeibel-Palade body located_inIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatWeibel-Palade body located_inISOVwf (Mus musculus)1624291 PMID:30573509RGDPMID:30573509
VwfRatWeibel-Palade body located_inIEAUniRule:UR0015287711600115GO_REF:0000104UniProtGO_REF:0000104
1 to 17 of 17 rows

Molecular Function
1 to 17 of 17 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatcollagen binding enablesIEAUniRule:UR0015287711600115GO_REF:0000104UniProtGO_REF:0000104
VwfRatcollagen binding enablesIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatcollagen binding enablesISOVWF (Homo sapiens)1624291 PMID:2056120RGDPMID:2056120
VwfRatidentical protein binding enablesISOVWF (Homo sapiens)1624291UniProtKB:P04275 more ...RGDPMID:10887119 more ...
VwfRatidentical protein binding enablesIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatidentical protein binding enablesIEAUniRule:UR0015287711600115GO_REF:0000104UniProtGO_REF:0000104
VwfRatimmunoglobulin binding enablesISOVWF (Homo sapiens)1624291 PMID:3121636RGDPMID:3121636
VwfRatimmunoglobulin binding enablesIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatintegrin binding enablesIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatintegrin binding enablesISOVWF (Homo sapiens)1624291UniProtKB:P13612 and PMID:9079671RGDPMID:9079671
VwfRatprotease binding enablesISOVWF (Homo sapiens)1624291UniProtKB:Q76LX8 more ...RGDPMID:12775718 and PMID:15824096
VwfRatprotease binding enablesIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
VwfRatprotein binding enablesISOVWF (Homo sapiens) and UniProtKB:P04275-21624291UniProtKB:Q12888 more ...RGDPMID:32814053
VwfRatprotein binding enablesISOVWF (Homo sapiens)1624291UniProtKB:P00451 more ...RGDPMID:11943773 more ...
VwfRatprotein binding enablesISOVwf (Mus musculus)1624291PR:P55002 PMID:18281502RGDPMID:18281502
VwfRatprotein-folding chaperone binding enablesISOVWF (Homo sapiens)1624291 PMID:10887119RGDPMID:10887119
VwfRatprotein-folding chaperone binding enablesIEAUniProtKB:P04275 and ensembl:ENSP000002614051600115GO_REF:0000107EnsemblGO_REF:0000107
1 to 17 of 17 rows

RGD Manual Annotations


  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatplatelet aggregation pathway  ISOVWF (Homo sapiens)1580446 RGD 

Imported Annotations - KEGG (archival)

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VwfRatcell-extracellular matrix signaling pathway  IEA 6907045 KEGGrno:04512
VwfRatcoagulation cascade pathway   IEA 6907045 KEGGrno:04610
VwfRatcomplement system pathway  IEA 6907045 KEGGrno:04610

1 to 20 of 73 rows
#
Reference Title
Reference Citation
1. Small bowel ischaemia-reperfusion increases plasma concentrations of oxidised proteins in rats. Abu-Zidan FM, etal., Eur J Surg. 1999 Apr;165(4):383-9.
2. Baseline vWF factor predicts the development of elevated pulmonary artery pressure in systemic sclerosis. Barnes T, etal., Rheumatology (Oxford). 2012 Sep;51(9):1606-9. Epub 2012 May 16.
3. Von Willebrand factor in plasma and in liver tissue after partial hepatectomy in the rat. Baruch Y, etal., J Hepatol 2002 Oct;37(4):471-7.
4. The genetic association database. Becker KG, etal., Nat Genet. 2004 May;36(5):431-2.
5. Fibrin polymerization is crucial for thrombin generation in platelet-rich plasma in a VWF-GPIb-dependent process, defective in Bernard-Soulier syndrome. Beguin S, etal., J Thromb Haemost. 2004 Jan;2(1):170-6.
6. The vascular biology of the glycoprotein Ib-IX-V complex. Berndt MC, etal., Thromb Haemost. 2001 Jul;86(1):178-88.
7. Von Willebrand factor antigen levels in Behcet disease. Beyan E, etal., Am J Hematol. 2005 May;79(1):70-2.
8. Increased deposition of von Willebrand factor in the rat heart after local ionizing irradiation. Boerma M, etal., Strahlenther Onkol. 2004 Feb;180(2):109-16.
9. Hypoxia and altered platelet behavior influence von Willebrand factor multimeric composition in secondary pulmonary hypertension. Caramuru LH, etal., Clin Appl Thromb Hemost. 2003 Jul;9(3):251-8.
10. Rosiglitazone does not improve vascular function in subjects with chronic kidney disease. Chan DT, etal., Nephrol Dial Transplant. 2011 Nov;26(11):3543-9. doi: 10.1093/ndt/gfr049. Epub 2011 Mar 4.
11. Variable content of von Willebrand factor mutant monomer drives the phenotypic variability in a family with von Willebrand disease. Chen J, etal., Blood. 2015 Jul 9;126(2):262-9. doi: 10.1182/blood-2014-11-613935. Epub 2015 May 27.
12. Effect of abdominal obesity on prothrombotic tendency in type 2 diabetes. Behavior of clotting factors VII and VIII, fibrinogen and von Willebrand Factor. Coca M, etal., Rom J Intern Med. 2005;43(1-2):115-26.
13. Oxidation of Met1606 in von Willebrand factor is a risk factor for thrombotic and septic complications in chronic renal failure. De Filippis V, etal., Biochem J. 2012 Mar 1;442(2):423-32. doi: 10.1042/BJ20111798.
14. Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor. Eikenboom JC, etal., Blood. 1996 Oct 1;88(7):2433-41.
15. Small intestinal production of nitric oxide is decreased following resuscitated hemorrhage. Fruchterman TM, etal., J Surg Res. 1998 Nov;80(1):102-9.
16. Circulating thrombomodulin and hematological alterations in type 2 diabetic patients with retinopathy. Fujiwara Y, etal., J Atheroscler Thromb. 1998;5(1):21-8.
17. Long Non-coding RNA MALAT1/microRNA-143/VEGFA Signal Axis Modulates Vascular Endothelial Injury-Induced Intracranial Aneurysm. Gao G, etal., Nanoscale Res Lett. 2020 Jun 29;15(1):139. doi: 10.1186/s11671-020-03357-2.
18. Effects of Radix et Rhizoma Rhodiolae Kirilowii on expressions of von Willebrand factor, hypoxia-inducible factor 1 and vascular endothelial growth factor in myocardium of rats with acute myocardial infarction. Gao XF, etal., Zhong Xi Yi Jie He Xue Bao. 2009 May;7(5):434-40. doi: 10.3736/jcim20090507.
19. 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.
20. Hemostatic efficacy, safety, and pharmacokinetics of a recombinant von Willebrand factor in severe von Willebrand disease. Gill JC, etal., Blood. 2015 Oct 22;126(17):2038-46. doi: 10.1182/blood-2015-02-629873. Epub 2015 Aug 3.
1 to 20 of 73 rows
PMID:2056120   PMID:3082891   PMID:3087627   PMID:3121636   PMID:6754744   PMID:7721887   PMID:7854452   PMID:8562500   PMID:8565074   PMID:8874190   PMID:9079671   PMID:9689113  
PMID:10764791   PMID:10887119   PMID:10930441   PMID:11071623   PMID:12775718   PMID:12871266   PMID:15824096   PMID:16409464   PMID:16551580   PMID:16735600   PMID:17380206   PMID:17895385  
PMID:18182488   PMID:18433458   PMID:18492805   PMID:19056867   PMID:21037087   PMID:21592973   PMID:21857647   PMID:23376485   PMID:23979707   PMID:24006456   PMID:27068509   PMID:27224245  



Vwf
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr84160,042,900 - 160,177,757 (+)NCBIGRCr8
mRatBN7.24158,360,152 - 158,491,539 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl4158,360,152 - 158,491,539 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx4164,595,998 - 164,727,404 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.04160,378,929 - 160,510,343 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.04159,012,985 - 159,144,157 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.04158,085,059 - 158,219,525 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl4158,088,505 - 158,219,523 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04225,098,521 - 225,229,257 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44161,723,415 - 161,854,766 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.14162,053,065 - 162,055,090 (+)NCBI
Celera4147,092,791 - 147,223,711 (+)NCBICelera
Cytogenetic Map4q42NCBI
VWF
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38125,948,877 - 6,124,670 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl125,948,877 - 6,124,770 (-)EnsemblGRCh38hg38GRCh38
GRCh37126,058,043 - 6,233,836 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36125,928,301 - 6,104,097 (-)NCBINCBI36Build 36hg18NCBI36
Build 34125,928,307 - 6,104,097NCBI
Celera127,677,686 - 7,853,476 (-)NCBICelera
Cytogenetic Map12p13.31NCBI
HuRef125,910,003 - 6,085,514 (-)NCBIHuRef
CHM1_1126,057,433 - 6,233,298 (-)NCBICHM1_1
T2T-CHM13v2.0125,956,421 - 6,132,275 (-)NCBIT2T-CHM13v2.0
Vwf
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm396125,529,911 - 125,663,642 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl6125,523,737 - 125,663,642 (+)EnsemblGRCm39 Ensembl
GRCm386125,552,948 - 125,686,679 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl6125,546,774 - 125,686,679 (+)EnsemblGRCm38mm10GRCm38
MGSCv376125,502,981 - 125,636,695 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv366125,520,072 - 125,652,161 (+)NCBIMGSCv36mm8
Celera6127,212,807 - 127,346,911 (+)NCBICelera
Cytogenetic Map6F3NCBI
cM Map659.32NCBI
Vwf
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554133,672,470 - 3,819,571 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554133,672,470 - 3,825,588 (-)NCBIChiLan1.0ChiLan1.0
VWF
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21011,504,401 - 11,680,404 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11211,501,159 - 11,677,162 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0126,073,836 - 6,249,806 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1125,990,612 - 6,166,632 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl125,990,612 - 6,165,153 (-)Ensemblpanpan1.1panPan2
VWF
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12738,834,812 - 38,972,614 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2738,833,837 - 39,320,142 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha277,641,828 - 7,779,174 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02739,191,850 - 39,329,540 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2739,193,140 - 39,329,536 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12739,062,625 - 39,200,071 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02739,104,190 - 39,241,989 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0277,119,622 - 7,257,688 (-)NCBIUU_Cfam_GSD_1.0
Vwf
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404945102,910,587 - 103,074,328 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367091,579,096 - 1,741,754 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049367091,578,137 - 1,741,877 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
VWF
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl564,517,555 - 64,655,938 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1564,516,627 - 64,655,938 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2566,999,793 - 67,078,133 (+)NCBISscrofa10.2Sscrofa10.2susScr3
Pig Cytomap5q21NCBI
VWF
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1115,994,499 - 6,176,949 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl115,994,039 - 6,162,260 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660632,072,116 - 2,236,240 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Vwf
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248602,858,088 - 2,973,052 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248602,843,268 - 2,973,888 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

.
Variants in Vwf
1377 total Variants

Predicted Target Of
Summary Value
Count of predictions:61
Count of miRNA genes:56
Interacting mature miRNAs:60
Transcripts:ENSRNOT00000026643
Prediction methods: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 38 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
6478754Anxrr43Anxiety related response QTL 430.14035locomotor behavior trait (VT:0001392)distance moved per unit of time into, out of or within a discrete space in an experimental apparatus (CMO:0001493)4144639524182687754Rat
724558Plsm2Polydactyly-luxate syndrome (PLS) morphotypes QTL 20.0003hindlimb integrity trait (VT:0010563)hind foot phalanges count (CMO:0001949)4132422778177422778Rat
1582237Kidm34Kidney mass QTL 3440.0001kidney mass (VT:0002707)both kidneys wet weight to body weight ratio (CMO:0000340)4148090542168069246Rat
6478693Anxrr32Anxiety related response QTL 320.00092locomotor behavior trait (VT:0001392)measurement of voluntary locomotion into, out of or within a discrete space in an experimental apparatus (CMO:0000957)4144639524182687754Rat
10755501Bp390Blood pressure QTL 3902.5arterial blood pressure trait (VT:2000000)diastolic blood pressure (CMO:0000005)426775591168368347Rat
631683Bp116Blood pressure QTL 1160.0001arterial blood pressure trait (VT:2000000)systolic blood pressure (CMO:0000004)4124303370169303370Rat
61451Ciaa4CIA Autoantibody QTL 43.1blood autoantibody amount (VT:0003725)calculated serum anti-rat type 2 collagen autoantibody titer (CMO:0001281)4126395976167139601Rat
1331738Bp209Blood pressure QTL 2092.979arterial blood pressure trait (VT:2000000)mean arterial blood pressure (CMO:0000009)4138503169179293946Rat
6478700Anxrr33Anxiety related response QTL 330.00896locomotor behavior trait (VT:0001392)amount of experiment time spent in a discrete space in an experimental apparatus (CMO:0000958)4144639524182687754Rat
1298524Oia8Oil induced arthritis QTL 8joint integrity trait (VT:0010548)joint inflammation composite score (CMO:0000919)4138503169173369699Rat

1 to 10 of 38 rows
D4Wox36  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.24158,447,303 - 158,447,479 (+)MAPPERmRatBN7.2
Rnor_6.04158,175,129 - 158,175,304NCBIRnor6.0
Rnor_5.04225,185,117 - 225,185,292UniSTSRnor5.0
RGSC_v3.44161,808,751 - 161,808,926UniSTSRGSC3.4
Celera4147,179,655 - 147,179,830UniSTS
Cytogenetic Map4q42UniSTS
Vwf  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.24158,447,823 - 158,448,025 (+)MAPPERmRatBN7.2
Rnor_6.04158,175,649 - 158,175,850NCBIRnor6.0
Rnor_5.04225,185,637 - 225,185,838UniSTSRnor5.0
RGSC_v3.44161,809,271 - 161,809,472UniSTSRGSC3.4
Celera4147,180,175 - 147,180,376UniSTS
Cytogenetic Map4q42UniSTS
RH132777  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.24158,491,246 - 158,491,439 (+)MAPPERmRatBN7.2
Rnor_6.04158,219,233 - 158,219,425NCBIRnor6.0
Rnor_5.04225,228,965 - 225,229,157UniSTSRnor5.0
RGSC_v3.44161,854,469 - 161,854,661UniSTSRGSC3.4
Celera4147,223,419 - 147,223,611UniSTS
Cytogenetic Map4q42UniSTS


This gene Vwf 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: ENSRNOT00000026643   ⟹   ENSRNOP00000026643
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl4158,360,152 - 158,491,539 (+)Ensembl
Rnor_6.0 Ensembl4158,088,505 - 158,219,523 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000116998   ⟹   ENSRNOP00000084421
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl4158,394,481 - 158,491,539 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000117299   ⟹   ENSRNOP00000091836
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl4158,361,767 - 158,491,539 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000118023   ⟹   ENSRNOP00000079544
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl4158,381,564 - 158,491,539 (+)Ensembl
RefSeq Acc Id: NM_053889   ⟹   NP_446341
RefSeq Status: VALIDATED
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr84160,046,369 - 160,177,757 (+)NCBI
mRatBN7.24158,360,152 - 158,491,539 (+)NCBI
Rnor_6.04158,088,533 - 158,219,525 (+)NCBI
Rnor_5.04225,098,521 - 225,229,257 (+)NCBI
Celera4147,092,791 - 147,223,711 (+)NCBI
Sequence:
RefSeq Acc Id: XM_063285420   ⟹   XP_063141490
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr84160,042,900 - 160,177,757 (+)NCBI
1 to 9 of 9 rows
Protein RefSeqs NP_446341 (Get FASTA)   NCBI Sequence Viewer  
  XP_063141490 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA96311 (Get FASTA)   NCBI Sequence Viewer  
  AAB39496 (Get FASTA)   NCBI Sequence Viewer  
  CAB37852 (Get FASTA)   NCBI Sequence Viewer  
  DAA34810 (Get FASTA)   NCBI Sequence Viewer  
  EDM01842 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000026643
GenBank Protein Q62935 (Get FASTA)   NCBI Sequence Viewer  
1 to 9 of 9 rows
RefSeq Acc Id: NP_446341   ⟸   NM_053889
- Peptide Label: precursor
- UniProtKB: A0A8J8XVZ5 (UniProtKB/TrEMBL),   A6ILU6 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSRNOP00000026643   ⟸   ENSRNOT00000026643
Ensembl Acc Id: ENSRNOP00000091836   ⟸   ENSRNOT00000117299
Ensembl Acc Id: ENSRNOP00000084421   ⟸   ENSRNOT00000116998
Ensembl Acc Id: ENSRNOP00000079544   ⟸   ENSRNOT00000118023
CTCK   VWFA   VWFC   VWFD

Name Modeler Protein Id AA Range Protein Structure
AF-Q62935-F1-model_v2 AlphaFold Q62935 1-430 view protein structure


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

RGD ID:13693414
Promoter ID:EPDNEW_R3939
Type:single initiation site
Name:Vwf_1
Description:von Willebrand factor
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_6.04158,088,533 - 158,088,593EPDNEW


1 to 28 of 28 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-42984 BioCyc
Ensembl Genes ENSRNOG00000019689 Ensembl, ENTREZGENE
Ensembl Transcript ENSRNOT00000026643 ENTREZGENE
Gene3D-CATH 3.40.50.410 UniProtKB/Swiss-Prot
InterPro ECM_Assembly_Org UniProtKB/Swiss-Prot
  VWA_N2 UniProtKB/Swiss-Prot
  VWF_A UniProtKB/Swiss-Prot
  vWFA_dom_sf UniProtKB/Swiss-Prot
NCBI Gene 116669 ENTREZGENE
PANTHER COLLAGEN ALPHA UniProtKB/Swiss-Prot
  VWFA DOMAIN-CONTAINING PROTEIN UniProtKB/Swiss-Prot
Pfam VWA UniProtKB/Swiss-Prot
  VWA_N2 UniProtKB/Swiss-Prot
PhenoGen Vwf PhenoGen
PRINTS VWFADOMAIN UniProtKB/Swiss-Prot
PROSITE VWFA UniProtKB/Swiss-Prot
RatGTEx ENSRNOG00000019689 RatGTEx
SMART VWA UniProtKB/Swiss-Prot
Superfamily-SCOP SSF53300 UniProtKB/Swiss-Prot
UniProt A0A8I5ZNS8_RAT UniProtKB/TrEMBL
  A0A8I6A191_RAT UniProtKB/TrEMBL
  A0A8I6AF98_RAT UniProtKB/TrEMBL
  A0A8J8XVZ5 ENTREZGENE, UniProtKB/TrEMBL
  A6ILU6 ENTREZGENE, UniProtKB/TrEMBL
  F1M957_RAT UniProtKB/TrEMBL
  Q62935 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary Q78E31 UniProtKB/Swiss-Prot
  Q9Z0P2 UniProtKB/Swiss-Prot
1 to 28 of 28 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2010-05-25 Vwf  von Willebrand factor  Vwf  von Willebrand factor homolog  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2009-10-22 Vwf  von Willebrand factor homolog  Vwf  Von Willebrand factor homolog  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2008-05-15 Vwf  Von Willebrand factor homolog  Vwf  von Willebrand factor  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2006-03-30 Vwf  von Willebrand factor      Symbol and Name status set to approved 1299863 APPROVED
2002-08-07 Vwf  Von Willebrand factor      Symbol and Name status set to provisional 70820 PROVISIONAL

Note Type Note Reference
gene_expression protein levels increase after partial hepatectomy 727737