F12 (coagulation factor XII) - Rat Genome Database

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Gene: F12 (coagulation factor XII) Rattus norvegicus
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Symbol: F12
Name: coagulation factor XII
RGD ID: 1359175
Description: Predicted to enable serine-type endopeptidase activity. Predicted to be involved in several processes, including positive regulation of plasminogen activation; protein maturation; and regulation of blood coagulation. Located in extracellular space. Used to study hyperhomocysteinemia. Human ortholog(s) of this gene implicated in angioedema (multiple); cerebrovascular disease (multiple); factor XII deficiency; and myocardial infarction. Orthologous to human F12 (coagulation factor XII); PARTICIPATES IN coagulation cascade pathway; acenocoumarol pharmacodynamics pathway; alteplase pharmacodynamics pathway; INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 2,4-dinitrotoluene; 2,6-dinitrotoluene.
Type: protein-coding
RefSeq Status: PROVISIONAL
Previously known as: coagulation factor XII (Hageman factor); factor XII; HAF; hageman factor; LOC306761; similar to coagulation factor XII (Hageman factor)
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
GRCr8179,212,819 - 9,220,664 (+)NCBIGRCr8
mRatBN7.2179,207,683 - 9,215,530 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl179,207,683 - 9,215,530 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx179,223,730 - 9,231,646 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01710,753,767 - 10,761,675 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0179,220,120 - 9,228,036 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0179,736,577 - 9,744,420 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl179,736,577 - 9,744,420 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01711,845,561 - 11,853,600 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41715,251,611 - 15,259,583 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11715,251,610 - 15,259,583 (+)NCBI
Celera179,286,222 - 9,294,037 (+)NCBICelera
Cytogenetic Map17p14NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Original Reference(s)
F12Ratacquired angioedema disease_progressionISOF12 (Homo sapiens)11565081 RGD 
F12Ratangioedema  ISOF12 (Homo sapiens)1601106DNA:missense:exon:T309K and T309RRGD 
F12RatCoronary Disease  ISOF12 (Homo sapiens)11041785protein:decreased activity::RGD 
F12RatDeath  ISOF12 (Homo sapiens)11041782 RGD 
F12RatEndotoxemia  IEP 7394782 RGD 
F12Ratfactor XII deficiency  ISOF12 (Homo sapiens)11041805DNA:deletion mutations more ...RGD 
F12Ratfactor XII deficiency  ISOF12 (Homo sapiens)11041772DNA:missense more ...RGD 
F12Ratfactor XII deficiency  ISOF12 (Homo sapiens)1601107DNA:missense:exon:C571SRGD 
F12Ratfactor XII deficiency  ISOF12 (Homo sapiens)11041769DNA:polymorphism:promoter:-46C>T(human)RGD 
F12Rathereditary angioedema  ISOF12 (Homo sapiens)11041802DNA:deletion mutations:exon and intron:RGD 
F12Rathereditary angioedema disease_progressionISOF12 (Homo sapiens)11565081 RGD 
F12Rathyperhomocysteinemia treatmentIDA 1601105 RGD 
F12Ratmiddle cerebral artery infarction treatmentISOF12 (Homo sapiens)11041786 RGD 
F12Ratmiddle cerebral artery infarction  ISOF12 (Mus musculus)11041786 RGD 
F12Ratmyocardial infarction susceptibilityISOF12 (Homo sapiens)11041803DNA:polymorphism:promoter:-46C>T(human)RGD 
F12RatSpontaneous Abortions  ISOF12 (Homo sapiens)11041799protein:decreased activity: :RGD 
F12RatStroke susceptibilityISOF12 (Homo sapiens)11041862DNA:polymorphism::46C>T(human)RGD 
F12RatThromboembolism  ISOF12 (Homo sapiens)11041771 RGD 
F12RatThromboembolism  ISOF12 (Mus musculus)11041771 RGD 
F12Rattransient cerebral ischemia treatmentISOF12 (Homo sapiens)11041786 RGD 
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Original Reference(s)
F12Ratangioedema  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: AngioedemaClinVarPMID:16638441 and PMID:25741868
F12Ratbilirubin metabolic disorder  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: HyperbilirubinemiaClinVarPMID:16638441 and PMID:25741868
F12RatC1 inhibitor deficiency  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: C1 ESTERASE INHIBITOR DEFICIENCYClinVarPMID:10984376 more ...
F12RatEhlers-Danlos syndrome dermatosparaxis type  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: Ehlers-Danlos syndrome and dermatosparaxis typeClinVarPMID:16770806 more ...
F12RatEhlers-Danlos syndrome spondylodysplastic type 2  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: Ehlers-Danlos syndrome progeroid typeClinVarPMID:28492532
F12Ratfactor XII deficiency  ISOF12 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10361128 more ...
F12Ratgenetic disease  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:25741868 and PMID:28492532
F12Rathereditary angioedema  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: Hereditary angioneurotic edemaClinVarPMID:10984376 more ...
F12Rathereditary angioedema type I  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: ANGIOEDEMA more ...ClinVarPMID:10984376 more ...
F12Rathereditary angioedema type III  ISOF12 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10361128 more ...
F12Rathypertension  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: HypertensionClinVarPMID:16638441 and PMID:25741868
F12Rathypophosphatemic nephrolithiasis/osteoporosis  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: Nephrolithiasis/osteoporosis and hypophosphatemicClinVarPMID:24033266 more ...
F12Rathypophosphatemic nephrolithiasis/osteoporosis 1  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: Hypophosphatemic nephrolithiasis/osteoporosis 1ClinVarPMID:25050900 more ...
F12RatMarfanoid Mental Retardation Syndrome, Autosomal  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: Marfanoid habitus and intellectual disabilityClinVarPMID:25741868
F12RatSilver-Russell syndrome  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: Russell-Silver syndromeClinVarPMID:27172843
F12RatSotos syndrome  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: Sotos syndromeClinVarPMID:12464997 more ...
F12Ratthrombosis  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: ThrombusClinVarPMID:25741868
F12Raturticaria  ISOF12 (Homo sapiens)8554872ClinVar Annotator: match by term: UrticariaClinVarPMID:16638441 and PMID:25741868
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Original Reference(s)
F12RatExperimental Liver Neoplasms  ISOF12 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:11420682
F12Ratfactor XII deficiency  ISOF12 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
F12Rathereditary angioedema  ISOF12 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19477491
F12Rathereditary angioedema type III  ISOF12 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
F12Rathypertension  ISOF12 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:6383834
F12RatThromboembolism  ISOF12 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:16009717
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Original Reference(s)
F12Ratfactor XII deficiency  ISSF12 (Mus musculus)13592920OMIM:234000MouseDO 
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Original Reference(s)
F12Ratfactor XII deficiency  ISOF12 (Homo sapiens)7240710 OMIM 
F12Rathereditary angioedema type III  ISOF12 (Homo sapiens)7240710 OMIM 

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Original Reference(s)
F12Rat(1->4)-beta-D-glucan multiple interactionsISOF12 (Mus musculus)6480464[perfluorooctane sulfonic acid co-treated with Cellulose] results in decreased expression of F12 mRNACTDPMID:36331819
F12Rat17beta-estradiol increases expressionISOF12 (Mus musculus)6480464Estradiol results in increased expression of F12 mRNACTDPMID:39298647
F12Rat2,3',4,4',5-Pentachlorobiphenyl increases expressionISOF12 (Mus musculus)64804642 more ...CTDPMID:31388691
F12Rat2,3,7,8-tetrachlorodibenzodioxine multiple interactionsISOF12 (Homo sapiens)6480464Cycloheximide inhibits the reaction [Tetrachlorodibenzodioxin results in decreased expression of F12 mRNA]CTDPMID:11007951
F12Rat2,3,7,8-tetrachlorodibenzodioxine affects expressionISOF12 (Mus musculus)6480464Tetrachlorodibenzodioxin affects the expression of F12 mRNACTDPMID:21570461
F12Rat2,3,7,8-tetrachlorodibenzodioxine decreases expressionEXP 6480464Tetrachlorodibenzodioxin results in decreased expression of F12 mRNACTDPMID:21215274
F12Rat2,3,7,8-tetrachlorodibenzodioxine decreases expressionISOF12 (Homo sapiens)6480464Tetrachlorodibenzodioxin results in decreased expression of F12 mRNACTDPMID:11007951
F12Rat2,4-dibromophenyl 2,4,5-tribromophenyl ether affects expressionISOF12 (Mus musculus)64804642 more ...CTDPMID:38648751
F12Rat2,4-dinitrotoluene affects expressionEXP 64804642 and 4-dinitrotoluene affects the expression of F12 mRNACTDPMID:21346803
F12Rat2,6-dinitrotoluene affects expressionEXP 64804642 and 6-dinitrotoluene affects the expression of F12 mRNACTDPMID:21346803
F12Rat4,4'-sulfonyldiphenol increases expressionISOF12 (Mus musculus)6480464bisphenol S results in increased expression of F12 mRNACTDPMID:39298647
F12Rat4,4'-sulfonyldiphenol affects methylationISOF12 (Mus musculus)6480464bisphenol S affects the methylation of F12 geneCTDPMID:31683443
F12Rat5-aza-2'-deoxycytidine affects expressionISOF12 (Homo sapiens)6480464Decitabine affects the expression of F12 mRNACTDPMID:23300844
F12Rat5-fluorouracil affects response to substanceISOF12 (Homo sapiens)6480464F12 protein affects the susceptibility to FluorouracilCTDPMID:15352031
F12Rat5-fluorouracil decreases expressionISOF12 (Homo sapiens)6480464Fluorouracil results in decreased expression of F12 proteinCTDPMID:15352031
F12Rat6-propyl-2-thiouracil decreases expressionEXP 6480464Propylthiouracil results in decreased expression of F12 mRNACTDPMID:24780913
F12Ratacetamide decreases expressionEXP 6480464acetamide results in decreased expression of F12 mRNACTDPMID:31881176
F12Ratacrylamide increases expressionEXP 6480464Acrylamide results in increased expression of F12 mRNACTDPMID:28959563
F12Rataflatoxin B1 affects expressionISOF12 (Homo sapiens)6480464Aflatoxin B1 affects the expression of F12 proteinCTDPMID:20106945
F12Rataflatoxin B1 decreases expressionISOF12 (Homo sapiens)6480464Aflatoxin B1 results in decreased expression of F12 mRNACTDPMID:27153756

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Biological Process
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Original Reference(s)
F12Ratblood coagulation involved_inIEAUniProtKB-KW:KW-00941600115GO_REF:0000043UniProtGO_REF:0000043
F12Ratblood coagulation acts_upstream_of_or_withinISOF12 (Mus musculus)1624291MGI:3720935 PMID:15351846RGDPMID:15351846
F12Ratblood coagulation acts_upstream_of_or_withinIEAUniProtKB:Q80YC5 and ensembl:ENSMUSP000000219481600115GO_REF:0000107EnsemblGO_REF:0000107
F12Ratblood coagulation involved_inIBAMGI:1891012 and PANTHER:PTN0028000211600115GO_REF:0000033GO_CentralGO_REF:0000033
F12RatFactor XII activation involved_inIEAUniProtKB:P00748 and ensembl:ENSP000002534961600115GO_REF:0000107EnsemblGO_REF:0000107
F12RatFactor XII activation involved_inISOF12 (Homo sapiens)1624291 PMID:18725990RGDPMID:18725990
F12Ratfibrinolysis involved_inIEAUniProtKB-KW:KW-02801600115GO_REF:0000043UniProtGO_REF:0000043
F12Rathemostasis involved_inIEAUniProtKB-KW:KW-03561600115GO_REF:0000043UniProtGO_REF:0000043
F12Ratplasma kallikrein-kinin cascade involved_inISOF12 (Homo sapiens)1624291 PMID:18725990 and PMID:6793628RGDPMID:18725990 and PMID:6793628
F12Ratplasma kallikrein-kinin cascade involved_inIEAUniProtKB:P00748 and ensembl:ENSP000002534961600115GO_REF:0000107EnsemblGO_REF:0000107
F12Ratpositive regulation of blood coagulation involved_inIEAUniProtKB:P00748 and ensembl:ENSP000002534961600115GO_REF:0000107EnsemblGO_REF:0000107
F12Ratpositive regulation of blood coagulation involved_inISOF12 (Homo sapiens)1624291 PMID:6793628RGDPMID:6793628
F12Ratpositive regulation of fibrinolysis involved_inIEAUniProtKB:P00748 and ensembl:ENSP000002534961600115GO_REF:0000107EnsemblGO_REF:0000107
F12Ratpositive regulation of fibrinolysis involved_inISOF12 (Homo sapiens)1624291 PMID:89876RGDPMID:89876
F12Ratpositive regulation of plasminogen activation involved_inIEAUniProtKB:P00748 and ensembl:ENSP000002534961600115GO_REF:0000107EnsemblGO_REF:0000107
F12Ratpositive regulation of plasminogen activation involved_inISOF12 (Homo sapiens)1624291 PMID:89876RGDPMID:89876
F12Ratprotein autoprocessing involved_inISOF12 (Homo sapiens)1624291 PMID:18725990RGDPMID:18725990
F12Ratprotein autoprocessing involved_inIEAUniProtKB:P00748 and ensembl:ENSP000002534961600115GO_REF:0000107EnsemblGO_REF:0000107
F12Ratprotein processing involved_inISOF12 (Homo sapiens)1624291 PMID:18725990RGDPMID:18725990
F12Ratprotein processing involved_inIEAUniProtKB:P00748 and ensembl:ENSP000002534961600115GO_REF:0000107EnsemblGO_REF:0000107
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Cellular Component
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Original Reference(s)
F12Ratextracellular region located_inIEAInterPro:IPR0000831600115GO_REF:0000002InterProGO_REF:0000002
F12Ratextracellular region located_inIEAUniProtKB-KW:KW-09641600115GO_REF:0000043UniProtGO_REF:0000043
F12Ratextracellular region located_inIEAUniProtKB-SubCell:SL-02431600115GO_REF:0000044UniProtGO_REF:0000044
F12Ratextracellular space  IDA 11041779 RGD 
F12Ratextracellular space located_inIEAInterPro:IPR0143941600115GO_REF:0000002InterProGO_REF:0000002
F12Ratextracellular space located_inISOF12 (Mus musculus)1624291MGI:3720935 PMID:15351846RGDPMID:15351846
F12Ratextracellular space is_active_inIBAMGI:1891012 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
F12Ratextracellular space located_inISOF12 (Homo sapiens)1624291 PMID:6793628RGDPMID:6793628
F12Ratextracellular space located_inIEAUniProtKB:P00748 and ensembl:ENSP000002534961600115GO_REF:0000107EnsemblGO_REF:0000107
F12Ratextracellular space located_inIEAUniProtKB:Q80YC5 and ensembl:ENSMUSP000000219481600115GO_REF:0000107EnsemblGO_REF:0000107
F12Ratrough endoplasmic reticulum is_active_inIBAMGI:1859281 and PANTHER:PTN0025455961600115GO_REF:0000033GO_CentralGO_REF:0000033
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Molecular Function
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Original Reference(s)
F12Ratcalcium ion binding enablesIEAInterPro:IPR0018811600115GO_REF:0000002InterProGO_REF:0000002
F12Rathydrolase activity enablesIEAUniProtKB-KW:KW-03781600115GO_REF:0000043UniProtGO_REF:0000043
F12Ratpeptidase activity enablesIEAUniProtKB:Q80YC5 and ensembl:ENSMUSP000000219481600115GO_REF:0000107EnsemblGO_REF:0000107
F12Ratpeptidase activity enablesISOF12 (Mus musculus)1624291MGI:3720935 PMID:15351846RGDPMID:15351846
F12Ratpeptidase activity enablesIEAUniProtKB-KW:KW-06451600115GO_REF:0000043UniProtGO_REF:0000043
F12Ratprotein binding enablesISOF12 (Homo sapiens)1624291UniProtKB:A7BJ45 more ...RGDPMID:12011093 more ...
F12Ratserine-type endopeptidase activity enablesISOF12 (Homo sapiens)1624291 PMID:18725990 and PMID:6793628RGDPMID:18725990 and PMID:6793628
F12Ratserine-type endopeptidase activity enablesIEAEC:3.4.21.381600115GO_REF:0000003UniProtGO_REF:0000003
F12Ratserine-type endopeptidase activity enablesIEAInterPro:IPR001254 more ...1600115GO_REF:0000002InterProGO_REF:0000002
F12Ratserine-type endopeptidase activity enablesIBAMGI:102756 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
F12Ratserine-type endopeptidase activity enablesIEAInterPro:IPR0012541600115GO_REF:0000002InterProGO_REF:0000002
F12Ratserine-type endopeptidase activity enablesIEAUniProtKB:P00748 and ensembl:ENSP000002534961600115GO_REF:0000107EnsemblGO_REF:0000107
F12Ratserine-type peptidase activity enablesIEAUniProtKB-KW:KW-07201600115GO_REF:0000043UniProtGO_REF:0000043
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RGD Manual Annotations


  

Imported Annotations - SMPDB

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Original Reference(s)
F12Ratacenocoumarol pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00269
F12Ratalteplase pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00280
F12Rataminocaproic acid pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00286
F12Ratanistreplase pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00281
F12Rataprotinin pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00288
F12Ratargatroban pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00276
F12Ratbivalirudin pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00277
F12Ratdicoumarol pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00656
F12Ratdicoumarol pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00270
F12Ratenoxaparin pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00272
F12Ratfondaparinux pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00273
F12Ratheparin pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00274
F12Ratphenindione pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00655
F12Ratreteplase pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00285
F12Rattranexamic acid pharmacodynamics pathway  ISOF12 (Homo sapiens)10402751 SMPDBSMP:00287
F12Ratwarfarin pharmacodynamics pathway   ISOF12 (Homo sapiens)10402751 SMPDBSMP:00268
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Imported Annotations - KEGG (archival)

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F12Ratcoagulation cascade pathway   IEA 6907045 KEGGrno:04610
F12Ratcomplement system pathway  IEA 6907045 KEGGrno:04610

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Reference Title
Reference Citation
1. Coagulation factor XII (FXII) activity, activated FXII, distribution of FXII C46T gene polymorphism and coronary risk. Bach J, etal., J Thromb Haemost. 2008 Feb;6(2):291-6. Epub 2007 Nov 15.
2. A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor. Bork K, etal., Clin Immunol. 2011 Oct;141(1):31-5. doi: 10.1016/j.clim.2011.07.002. Epub 2011 Jul 30.
3. Human plasma prekallikrein, a zymogen to a serine protease that contains four tandem repeats. Chung DW, etal., Biochemistry 1986 May 6;25(9):2410-7.
4. Activation of the coagulation cascade in C1-inhibitor deficiencies. Cugno M, etal., Blood. 1997 May 1;89(9):3213-8.
5. Role of coagulation factor XII in unexplained recurrent abortions in the Greek population. Dendrinos S, etal., J Reprod Med. 2014 Jan-Feb;59(1-2):56-62.
6. Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor. Dewald G and Bork K, Biochem Biophys Res Commun. 2006 May 19;343(4):1286-9.
7. Folate deficiency-induced hyperhomocysteinemia attenuates, and folic acid supplementation restores, the functional activities of rat coagulation factors XII, X, and II. Ebbesen LS and Ingerslev J, J Nutr. 2005 Aug;135(8):1836-40.
8. Evidence of a U-shaped association between factor XII activity and overall survival. Endler G, etal., J Thromb Haemost. 2007 Jun;5(6):1143-8.
9. A common C-->T polymorphism at nt 46 in the promoter region of coagulation factor XII is associated with decreased factor XII activity. Endler G, etal., Thromb Res. 2001 Feb 15;101(4):255-60.
10. Paternal endothelial protein C receptor 219Gly variant as a mild and limited risk factor for deep vein thrombosis during pregnancy. Galanaud JP, etal., J Thromb Haemost. 2010 Apr;8(4):707-13. doi: 10.1111/j.1538-7836.2010.03770.x. Epub 2010 Feb 6.
11. 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.
12. Hepatocytes express blood coagulation factor XII (Hageman factor). Gordon EM, etal., J Lab Clin Med. 1990 Apr;115(4):463-9.
13. Targeting coagulation factor XII provides protection from pathological thrombosis in cerebral ischemia without interfering with hemostasis. Kleinschnitz C, etal., J Exp Med. 2006 Mar 20;203(3):513-8. Epub 2006 Mar 13.
14. Haemostatic abnormalities persist despite glycaemic improvement by insulin therapy in lean type 2 diabetic patients. Knobl P, etal., Thromb Haemost. 1994 Jun;71(6):692-7.
15. Molecular genetic analysis of Korean patients with coagulation factor XII deficiency. Kwon MJ, etal., Blood Coagul Fibrinolysis. 2010 Jun;21(4):308-12. doi: 10.1097/MBC.0b013e32833449df.
16. Rat ISS GO annotations from MGI mouse gene data--August 2006 MGD data from the GO Consortium
17. Coagulation factor XII (Hageman factor) Washington D.C.: inactive factor XIIa results from Cys-571----Ser substitution. Miyata T, etal., Proc Natl Acad Sci U S A. 1989 Nov;86(21):8319-22.
18. Molecular analysis of multiple genetic variants in Spanish FXII-deficient families. Mordillo C, etal., Haematologica. 2007 Nov;92(11):1569-72.
19. The kallikrein-kinin system: current and future pharmacological targets. Moreau ME, etal., J Pharmacol Sci. 2005 Sep;99(1):6-38.
20. Effect of dienogest on bleeding time, coagulation, fibrinolysis, and platelet aggregation in female rats. Nobukata H, etal., Toxicol Lett. 1999 Jan 11;104(1-2):93-101.
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PMID:89876   PMID:6793628   PMID:12477932   PMID:15351846   PMID:18725990   PMID:22216926   PMID:23376485   PMID:23533145   PMID:24733030  



F12
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8179,212,819 - 9,220,664 (+)NCBIGRCr8
mRatBN7.2179,207,683 - 9,215,530 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl179,207,683 - 9,215,530 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx179,223,730 - 9,231,646 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01710,753,767 - 10,761,675 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0179,220,120 - 9,228,036 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0179,736,577 - 9,744,420 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl179,736,577 - 9,744,420 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01711,845,561 - 11,853,600 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41715,251,611 - 15,259,583 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11715,251,610 - 15,259,583 (+)NCBI
Celera179,286,222 - 9,294,037 (+)NCBICelera
Cytogenetic Map17p14NCBI
F12
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385177,402,141 - 177,409,564 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5177,402,133 - 177,416,583 (-)EnsemblGRCh38hg38GRCh38
GRCh375176,829,142 - 176,836,565 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 365176,761,745 - 176,769,183 (-)NCBINCBI36Build 36hg18NCBI36
Build 345176,761,746 - 176,769,183NCBI
Celera5171,664,877 - 171,672,315 (+)NCBICelera
Cytogenetic Map5q35.3NCBI
HuRef5171,749,566 - 171,757,004 (-)NCBIHuRef
CHM1_15176,262,187 - 176,269,625 (-)NCBICHM1_1
T2T-CHM13v2.05177,945,359 - 177,952,782 (-)NCBIT2T-CHM13v2.0
F12
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391355,565,771 - 55,574,617 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1355,565,771 - 55,574,606 (-)EnsemblGRCm39 Ensembl
GRCm381355,417,958 - 55,426,804 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1355,417,958 - 55,426,793 (-)EnsemblGRCm38mm10GRCm38
MGSCv371355,519,327 - 55,528,163 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361355,427,610 - 55,436,409 (-)NCBIMGSCv36mm8
Celera1356,472,191 - 56,480,813 (-)NCBICelera
Cytogenetic Map13B1NCBI
cM Map1330.06NCBI
F12
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540829,642,096 - 29,650,950 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495540829,644,279 - 29,665,161 (-)NCBIChiLan1.0ChiLan1.0
F12
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v24172,486,323 - 172,511,069 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan15170,625,862 - 170,650,653 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v05172,703,724 - 172,711,618 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.15179,766,089 - 179,773,854 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl5179,766,243 - 179,773,485 (-)Ensemblpanpan1.1panPan2
F12
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1435,950,642 - 35,968,137 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl435,950,695 - 35,998,025 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha435,918,068 - 35,935,563 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0436,316,872 - 36,334,363 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl436,316,904 - 36,324,807 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1436,142,096 - 36,159,589 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0436,328,310 - 36,345,800 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0436,837,547 - 36,855,039 (+)NCBIUU_Cfam_GSD_1.0
F12
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213122,662,598 - 122,670,021 (-)NCBIHiC_Itri_2
SpeTri2.0NW_0049365971,687,511 - 1,694,782 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
F12
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl280,527,446 - 80,544,828 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1280,527,451 - 80,544,835 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
F12
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12379,414,074 - 79,438,896 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2379,414,225 - 79,432,298 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607510,603,660 - 10,619,663 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
F12
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473312,675,966 - 12,683,117 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473312,666,410 - 12,683,273 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

.
Variants in F12
81 total Variants

Predicted Target Of
Summary Value
Count of predictions:59
Count of miRNA genes:53
Interacting mature miRNAs:58
Transcripts:ENSRNOT00000066586
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 30 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
1354581Bp247Blood pressure QTL 2474.5arterial blood pressure trait (VT:2000000)pulse pressure (CMO:0000292)17169599340Rat
631499Stl1Serum triglyceride level QTL 13.6blood triglyceride amount (VT:0002644)blood triglyceride level (CMO:0000118)17327139827389946Rat
2293664Bmd28Bone mineral density QTL 285.10.0001femur mineral mass (VT:0010011)trabecular volumetric bone mineral density (CMO:0001729)17435448727028127Rat
1300123Bp194Blood pressure QTL 1942.82arterial blood pressure trait (VT:2000000)mean arterial blood pressure (CMO:0000009)17211514934551001Rat
1582224Epfw4Epididymal fat weight QTL 43.50.0058epididymal fat pad mass (VT:0010421)epididymal fat pad weight to body weight ratio (CMO:0000658)17920136523653323Rat
1582225Bw67Body weight QTL 676.20.0001body mass (VT:0001259)body weight (CMO:0000012)17920136523653323Rat
1582226Bw64Body weight QTL 644.20.0017body mass (VT:0001259)body weight (CMO:0000012)17920136523653323Rat
1354651Lmblg2Limb length QTL 26tibia length (VT:0004357)tibia length (CMO:0000450)17429913069599340Rat
10401807Kidm52Kidney mass QTL 52kidney mass (VT:0002707)both kidneys wet weight (CMO:0000085)17131701463Rat
10054088Scort28Serum corticosterone level QTL 282.040.0102blood corticosterone amount (VT:0005345)plasma corticosterone level (CMO:0001173)17452803849528038Rat

1 to 10 of 30 rows
BE102123  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2179,215,294 - 9,215,468 (+)MAPPERmRatBN7.2
Rnor_6.0179,744,185 - 9,744,358NCBIRnor6.0
Rnor_5.01711,853,365 - 11,853,538UniSTSRnor5.0
RGSC_v3.41715,259,348 - 15,259,521UniSTSRGSC3.4
Celera179,293,802 - 9,293,975UniSTS
RH 3.4 Map1779.5UniSTS
Cytogenetic Map17p14UniSTS
F12  
Rat AssemblyChrPosition (strand)SourceJBrowse
GRCr8179,220,182 - 9,220,500 (+)Marker Load Pipeline
mRatBN7.2179,215,048 - 9,215,366 (+)MAPPERmRatBN7.2
Rnor_6.0179,743,939 - 9,744,256NCBIRnor6.0
Rnor_5.01711,853,119 - 11,853,436UniSTSRnor5.0
RGSC_v3.41715,259,102 - 15,259,419UniSTSRGSC3.4
Celera179,293,556 - 9,293,873UniSTS
Cytogenetic Map17p14UniSTS




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 8 25 107 91 88 59 25 59 6 183 70 87 37 50 29



Ensembl Acc Id: ENSRNOT00000066586   ⟹   ENSRNOP00000061983
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl179,207,683 - 9,215,530 (+)Ensembl
Rnor_6.0 Ensembl179,736,577 - 9,744,420 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000081920   ⟹   ENSRNOP00000074115
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl179,207,683 - 9,215,530 (+)Ensembl
Rnor_6.0 Ensembl179,736,786 - 9,744,341 (+)Ensembl
RefSeq Acc Id: NM_001014006   ⟹   NP_001014028
RefSeq Status: PROVISIONAL
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8179,212,819 - 9,220,664 (+)NCBI
mRatBN7.2179,207,683 - 9,215,530 (+)NCBI
Rnor_6.0179,736,577 - 9,744,420 (+)NCBI
Rnor_5.01711,845,561 - 11,853,600 (+)NCBI
RGSC_v3.41715,251,611 - 15,259,583 (+)RGD
Celera179,286,222 - 9,294,037 (+)RGD
Sequence:
Protein RefSeqs NP_001014028 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH88187 (Get FASTA)   NCBI Sequence Viewer  
  D3ZTE0 (Get FASTA)   NCBI Sequence Viewer  
  EDL93987 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000061983
RefSeq Acc Id: NP_001014028   ⟸   NM_001014006
- Peptide Label: precursor
- UniProtKB: A0A0H2UI19 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSRNOP00000061983   ⟸   ENSRNOT00000066586
Ensembl Acc Id: ENSRNOP00000074115   ⟸   ENSRNOT00000081920
Name Modeler Protein Id AA Range Protein Structure
AF-D3ZTE0-F1-model_v2 AlphaFold D3ZTE0 1-595 view protein structure


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

RGD ID:13700316
Promoter ID:EPDNEW_R10829
Type:multiple initiation site
Name:F12_1
Description:coagulation factor XII
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_6.0179,736,750 - 9,736,810EPDNEW


1 to 40 of 66 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-10204 BioCyc
Ensembl Genes ENSRNOG00000015139 Ensembl, ENTREZGENE
Ensembl Transcript ENSRNOT00000066586 ENTREZGENE
Gene3D-CATH 2.10.10.10 UniProtKB/Swiss-Prot
  2.40.10.10 UniProtKB/Swiss-Prot
  2.40.20.10 UniProtKB/Swiss-Prot
  Laminin UniProtKB/Swiss-Prot
IMAGE_CLONE IMAGE:7370526 IMAGE-MGC_LOAD
InterPro Coagulation_fac_XII/HGFA UniProtKB/Swiss-Prot
  EGF-like_Ca-bd_dom UniProtKB/Swiss-Prot
  EGF-like_dom UniProtKB/Swiss-Prot
  Fibronectin_type1 UniProtKB/Swiss-Prot
  FN_type2_dom UniProtKB/Swiss-Prot
  FN_type2_sf UniProtKB/Swiss-Prot
  Kringle UniProtKB/Swiss-Prot
  Kringle-like UniProtKB/Swiss-Prot
  Kringle_CS UniProtKB/Swiss-Prot
  Kringle_sf UniProtKB/Swiss-Prot
  Peptidase_S1_PA UniProtKB/Swiss-Prot
  Peptidase_S1_PA_chymotrypsin UniProtKB/Swiss-Prot
  Peptidase_S1A UniProtKB/Swiss-Prot
  Serine_Proteases_S1 UniProtKB/Swiss-Prot
  Trypsin_dom UniProtKB/Swiss-Prot
  TRYPSIN_HIS UniProtKB/Swiss-Prot
  TRYPSIN_SER UniProtKB/Swiss-Prot
KEGG Report rno:306761 UniProtKB/Swiss-Prot
MGC_CLONE MGC:108855 IMAGE-MGC_LOAD
NCBI Gene 306761 ENTREZGENE
PANTHER COAGULATION FACTOR XII UniProtKB/Swiss-Prot
  TRYPSIN-RELATED UniProtKB/Swiss-Prot
Pfam EGF UniProtKB/Swiss-Prot
  fn1 UniProtKB/Swiss-Prot
  fn2 UniProtKB/Swiss-Prot
  Kringle UniProtKB/Swiss-Prot
  Trypsin UniProtKB/Swiss-Prot
PhenoGen F12 PhenoGen
PIRSF Factor_XII_HGFA UniProtKB/Swiss-Prot
PRINTS CHYMOTRYPSIN UniProtKB/Swiss-Prot
  FNTYPEII UniProtKB/Swiss-Prot
  KRINGLE UniProtKB/Swiss-Prot
1 to 40 of 66 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-20 F12  coagulation factor XII  F12  coagulation factor XII  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2016-01-20 F12  coagulation factor XII  F12  coagulation factor XII  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2016-01-20 F12  coagulation factor XII  F12  coagulation factor XII (Hageman factor)  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2006-03-30 F12  coagulation factor XII (Hageman factor)  LOC306761  similar to coagulation factor XII (Hageman factor); factor XII  Symbol and Name updated 1299863 APPROVED
2005-07-29 LOC306761  similar to coagulation factor XII (Hageman factor); factor XII      Symbol and Name status set to provisional 70820 PROVISIONAL