F13a1 (coagulation factor XIII A1 chain) - Rat Genome Database

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Gene: F13a1 (coagulation factor XIII A1 chain) Rattus norvegicus
Analyze
Symbol: F13a1
Name: coagulation factor XIII A1 chain
RGD ID: 621495
Description: Predicted to enable protein-glutamine gamma-glutamyltransferase activity. Predicted to be involved in blood coagulation, fibrin clot formation and peptide cross-linking. Predicted to act upstream of or within blood coagulation. Predicted to be located in cytoplasm and extracellular region. Biomarker of gastric ulcer. Human ortholog(s) of this gene implicated in artery disease (multiple); factor XIII deficiency; priapism; and thrombophilia (multiple). Orthologous to human F13A1 (coagulation factor XIII A chain); PARTICIPATES IN acenocoumarol pharmacodynamics pathway; alteplase pharmacodynamics pathway; aminocaproic acid pharmacodynamics pathway; INTERACTS WITH 2,2',4,4'-Tetrabromodiphenyl ether; 2,3,7,8-tetrachlorodibenzodioxine; 3,7-dihydropurine-6-thione.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: coagulation factor XIII A chain; coagulation factor XIII, A1 polypeptide; coagulation factor XIII, A1 subunit; coagulation factor XIIIa; F13a; protein-glutamine gamma-glutamyltransferase A chain; transglutaminase A chain
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
GRCr81728,021,197 - 28,197,960 (+)NCBIGRCr8
mRatBN7.21727,815,723 - 27,992,494 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1727,815,702 - 27,992,700 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1727,681,035 - 27,857,733 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01729,284,581 - 29,461,269 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01727,645,506 - 27,822,130 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01728,504,650 - 28,680,015 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1728,504,623 - 28,680,362 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01730,406,396 - 30,581,441 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41734,093,525 - 34,270,498 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11734,096,401 - 34,272,682 (+)NCBI
Celera1727,443,244 - 27,619,724 (+)NCBICelera
Cytogenetic Map17p12NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Original Reference(s)
F13a1Ratarteriosclerosis  ISOF13A1 (Homo sapiens)1581023 RGD 
F13a1RatB-lymphoblastic leukemia/lymphoma  ISOF13A1 (Homo sapiens)11041855protein:increased expression:B lymphoblast:RGD 
F13a1RatCerebral Hemorrhage  ISOF13A1 (Homo sapiens)1581027 RGD 
F13a1RatChemical and Drug Induced Liver Injury  ISOF13a1 (Mus musculus)11041813 RGD 
F13a1RatCoronary Disease  ISOF13A1 (Homo sapiens)1581030 RGD 
F13a1RatCrohn's disease  ISOF13A1 (Homo sapiens)10450739associated with Fistula and protein:decreased activity:plasma:RGD 
F13a1Ratdiabetic retinopathy  ISOF13A1 (Homo sapiens)8693344protein:increased expression:optic choroid vascular plexus:RGD 
F13a1Ratdisseminated intravascular coagulation  ISOF13A1 (Homo sapiens)1581020 RGD 
F13a1Ratfactor XIII deficiency  ISOF13A1 (Homo sapiens)11041869DNA:polymorphism:intron:IVS1+12C>A(human)RGD 
F13a1Ratfactor XIII deficiency  ISOF13A1 (Homo sapiens)10450727DNA:mutation:cds:p.R703W(human)RGD 
F13a1Ratfactor XIII deficiency  ISOF13A1 (Homo sapiens)10450726DNA:nonsense mutation:intron:RGD 
F13a1Ratfactor XIII deficiency  ISOF13A1 (Homo sapiens)10450730DNA:insertion and missense mutation:cds:RGD 
F13a1Ratfactor XIII deficiency  ISOF13A1 (Homo sapiens)10450729DNA:nonsense mutations and missense mutations:cds:RGD 
F13a1RatFactor XIII, A Subunit, Deficiency Of  ISOF13A1 (Homo sapiens)11041856DNA:deletions more ...RGD 
F13a1RatFactor XIII, A Subunit, Deficiency Of  ISOF13A1 (Homo sapiens)11041811DNA:nonsense more ...RGD 
F13a1Ratgastric ulcer  IEP 708325 RGD 
F13a1RatHemorrhage  ISOF13a1 (Mus musculus)11041809 RGD 
F13a1Ratmyocardial infarction  ISOF13A1 (Homo sapiens)1581022 RGD 
F13a1Ratpriapism susceptibilityISOF13A1 (Homo sapiens)10450728associated with sickle cell anemia and DNA:SNPs::multiple(human)RGD 
F13a1Ratpulmonary embolism  ISOF13A1 (Homo sapiens)1581021 RGD 
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F13a1Ratcombined oxidative phosphorylation deficiency 14  ISOF13A1 (Homo sapiens)8554872ClinVar Annotator: match by term: Combined oxidative phosphorylation deficiency 14ClinVarPMID:22833457 and PMID:28492532
F13a1Ratfactor XIII deficiency  ISOF13A1 (Homo sapiens)8554872ClinVar Annotator: match by term: Hereditary factor XIII deficiency diseaseClinVarPMID:31136071
F13a1RatFactor XIII, A Subunit, Deficiency Of  ISOF13A1 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10027709 more ...
F13a1Ratgenetic disease  ISOF13A1 (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:25741868 and PMID:28492532
F13a1Rathemorrhagic disease  ISOF13A1 (Homo sapiens)8554872ClinVar Annotator: match by term: Abnormal bleedingClinVar 
F13a1Ratmyocardial infarction  ISOF13A1 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10365735 more ...
F13a1Ratthrombophilia due to thrombin defect  ISOF13A1 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:22995991 more ...
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Original Reference(s)
F13a1Ratallergic contact dermatitis  ISOF13A1 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:17374397
F13a1Ratfactor XIII deficiency  ISOF13A1 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:1644910
F13a1RatFactor XIII, A Subunit, Deficiency Of  ISOF13A1 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
F13a1Ratmyocardial infarction  ISOF13A1 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:17393027
F13a1Ratthrombophilia  ISOF13A1 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
F13a1RatVenous Thrombosis  ISOF13A1 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:10365735
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Original Reference(s)
F13a1Ratfactor XIII deficiency  ISSF13a1 (Mus musculus)13592920OMIM:613225 more ...MouseDO 

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F13a1Rat(1->4)-beta-D-glucan multiple interactionsISOF13a1 (Mus musculus)6480464[perfluorooctane sulfonic acid co-treated with Cellulose] results in increased expression of F13A1 mRNACTDPMID:36331819
F13a1Rat1-chloro-2,4-dinitrobenzene decreases expressionISOF13A1 (Homo sapiens)6480464Dinitrochlorobenzene results in decreased expression of F13A1 mRNACTDPMID:17374397
F13a1Rat1-naphthyl isothiocyanate affects response to substanceISOF13a1 (Mus musculus)6480464F13A1 protein affects the susceptibility to 1-NaphthylisothiocyanateCTDPMID:26921287
F13a1Rat17beta-estradiol affects expressionISOF13A1 (Homo sapiens)6480464Estradiol affects the expression of F13A1 mRNACTDPMID:14699072
F13a1Rat17beta-estradiol increases expressionISOF13a1 (Mus musculus)6480464Estradiol results in increased expression of F13A1 mRNACTDPMID:19484750
F13a1Rat17beta-estradiol multiple interactionsISOF13A1 (Homo sapiens)6480464[Estradiol co-treated with Progesterone] results in decreased expression of F13A1 mRNA and [Progesterone co-treated with Estradiol] results in decreased expression of F13A1 mRNACTDPMID:17404688 and PMID:20660070
F13a1Rat2,2',4,4'-Tetrabromodiphenyl ether increases expressionEXP 64804642 more ...CTDPMID:27291303
F13a1Rat2,3,7,8-tetrachlorodibenzodioxine affects expressionISOF13a1 (Mus musculus)6480464Tetrachlorodibenzodioxin affects the expression of F13A1 mRNACTDPMID:21570461
F13a1Rat2,3,7,8-tetrachlorodibenzodioxine affects expressionEXP 6480464Tetrachlorodibenzodioxin affects the expression of F13A1 mRNACTDPMID:34747641
F13a1Rat2,3,7,8-tetrachlorodibenzodioxine increases expressionEXP 6480464Tetrachlorodibenzodioxin results in increased expression of F13A1 mRNACTDPMID:26232522 and PMID:32109520
F13a1Rat2,4-dibromophenyl 2,4,5-tribromophenyl ether increases expressionISOF13A1 (Homo sapiens)64804642 more ...CTDPMID:26705709
F13a1Rat2,4-dibromophenyl 2,4,5-tribromophenyl ether affects expressionISOF13a1 (Mus musculus)64804642 more ...CTDPMID:38648751
F13a1Rat3,4-methylenedioxymethamphetamine decreases methylationISOF13a1 (Mus musculus)6480464N-Methyl-3 and 4-methylenedioxyamphetamine results in decreased methylation of F13A1 promoterCTDPMID:26251327
F13a1Rat3,4-methylenedioxymethamphetamine increases expressionISOF13a1 (Mus musculus)6480464N-Methyl-3 and 4-methylenedioxyamphetamine results in increased expression of F13A1 mRNACTDPMID:26251327
F13a1Rat3,7-dihydropurine-6-thione increases expressionEXP 6480464Mercaptopurine results in increased expression of F13A1 mRNACTDPMID:23358152
F13a1Rat4,4'-sulfonyldiphenol increases expressionISOF13a1 (Mus musculus)6480464bisphenol S results in increased expression of F13A1 mRNACTDPMID:30951980
F13a1Rat4-(ethoxymethylene)-2-phenyloxazol-5-one decreases expressionISOF13A1 (Homo sapiens)6480464Oxazolone results in decreased expression of F13A1 mRNACTDPMID:17374397
F13a1Rat4-hydroxyphenyl retinamide decreases expressionISOF13a1 (Mus musculus)6480464Fenretinide results in decreased expression of F13A1 mRNACTDPMID:28973697
F13a1Rataflatoxin B1 increases methylationISOF13A1 (Homo sapiens)6480464Aflatoxin B1 results in increased methylation of F13A1 intronCTDPMID:30157460
F13a1Rataldehydo-D-glucose multiple interactionsISOF13a1 (Mus musculus)6480464[lard co-treated with Cholesterol and Dietary co-treated with Dietary Sucrose co-treated with Fructose co-treated with Glucose co-treated with Glyphosate] results in increased expression of F13A1 mRNACTDPMID:37567420

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Biological Process
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Original Reference(s)
F13a1Ratblood coagulation acts_upstream_of_or_withinIEAUniProtKB:Q8BH61 and ensembl:ENSMUSP000000486671600115GO_REF:0000107EnsemblGO_REF:0000107
F13a1Ratblood coagulation involved_inIEAUniProtKB-KW:KW-00941600115GO_REF:0000043UniProtGO_REF:0000043
F13a1Ratblood coagulation acts_upstream_of_or_withinISOF13a1 (Mus musculus)1624291MGI:2684302 PMID:12529747RGDPMID:12529747
F13a1Ratblood coagulation, fibrin clot formation involved_inIEAUniProtKB:P00488 and ensembl:ENSP000002648701600115GO_REF:0000107EnsemblGO_REF:0000107
F13a1Ratblood coagulation, fibrin clot formation involved_inISOF13a1 (Mus musculus)1624291MGI:5645817 PMID:18224415RGDPMID:18224415
F13a1Ratblood coagulation, fibrin clot formation involved_inIBAMGI:1921395 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
F13a1Ratblood coagulation, fibrin clot formation involved_inISOF13A1 (Homo sapiens)1624291 PMID:27363989RGDPMID:27363989
F13a1Ratblood coagulation, fibrin clot formation involved_inIEAUniProtKB:Q8BH61 and ensembl:ENSMUSP000000486671600115GO_REF:0000107EnsemblGO_REF:0000107
F13a1Ratblood coagulation, fibrin clot formation involved_inISSUniProtKB:P004881600115GO_REF:0000024UniProtGO_REF:0000024
F13a1Rathemostasis involved_inIEAUniProtKB-KW:KW-03561600115GO_REF:0000043UniProtGO_REF:0000043
F13a1Ratpeptide cross-linking involved_inISSUniProtKB:P004881600115GO_REF:0000024UniProtGO_REF:0000024
F13a1Ratpeptide cross-linking acts_upstream_of_or_withinISOF13a1 (Mus musculus)1624291 PMID:15507206RGDPMID:15507206
F13a1Ratpeptide cross-linking involved_inISOF13A1 (Homo sapiens)1624291 PMID:27363989RGDPMID:27363989
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Cellular Component

  
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F13a1Ratcytoplasm located_inIEAUniProtKB-SubCell:SL-00861600115GO_REF:0000044UniProtGO_REF:0000044
F13a1Ratcytoplasm located_inIEAUniProtKB-KW:KW-09631600115GO_REF:0000043UniProtGO_REF:0000043
F13a1Ratextracellular region located_inIEAUniProtKB-SubCell:SL-02431600115GO_REF:0000044UniProtGO_REF:0000044
F13a1Ratextracellular region located_inIEAUniProtKB-KW:KW-09641600115GO_REF:0000043UniProtGO_REF:0000043

Molecular Function
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F13a1Ratacyltransferase activity enablesIEAUniProtKB-KW:KW-00121600115GO_REF:0000043UniProtGO_REF:0000043
F13a1Ratmetal ion binding enablesIEAUniProtKB-KW:KW-04791600115GO_REF:0000043UniProtGO_REF:0000043
F13a1Ratprotein binding enablesISOF13A1 (Homo sapiens)1624291UniProtKB:O15273 more ...RGDPMID:32814053
F13a1Ratprotein-glutamine gamma-glutamyltransferase activity enablesIEAEC:2.3.2.131600115GO_REF:0000003UniProtGO_REF:0000003
F13a1Ratprotein-glutamine gamma-glutamyltransferase activity enablesIEAUniProtKB:P00488 and ensembl:ENSP000002648701600115GO_REF:0000107EnsemblGO_REF:0000107
F13a1Ratprotein-glutamine gamma-glutamyltransferase activity enablesIEAUniProtKB:Q8BH61 and ensembl:ENSMUSP000000486671600115GO_REF:0000107EnsemblGO_REF:0000107
F13a1Ratprotein-glutamine gamma-glutamyltransferase activity enablesIEARHEA:548161600115GO_REF:0000116RHEAGO_REF:0000116
F13a1Ratprotein-glutamine gamma-glutamyltransferase activity enablesIBAFB:FBgn0031975 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
F13a1Ratprotein-glutamine gamma-glutamyltransferase activity enablesISOF13a1 (Mus musculus)1624291MGI:2684302 more ...RGDPMID:12529747 and PMID:18224415
F13a1Ratprotein-glutamine gamma-glutamyltransferase activity enablesIEAInterPro:IPR008958 more ...1600115GO_REF:0000002InterProGO_REF:0000002
F13a1Ratprotein-glutamine gamma-glutamyltransferase activity enablesISSUniProtKB:P004881600115GO_REF:0000024UniProtGO_REF:0000024
F13a1Ratprotein-glutamine gamma-glutamyltransferase activity enablesISOF13A1 (Homo sapiens)1624291 PMID:27363989RGDPMID:27363989
F13a1Rattransferase activity enablesIEAUniProtKB-KW:KW-08081600115GO_REF:0000043UniProtGO_REF:0000043
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RGD Manual Annotations


  
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Original Reference(s)
F13a1Ratcoagulation cascade pathway   ISOF13A1 (Homo sapiens)11352259 RGD 

Imported Annotations - SMPDB

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F13a1Ratacenocoumarol pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00269
F13a1Ratalteplase pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00280
F13a1Rataminocaproic acid pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00286
F13a1Ratanistreplase pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00281
F13a1Rataprotinin pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00288
F13a1Ratargatroban pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00276
F13a1Ratbivalirudin pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00277
F13a1Ratdicoumarol pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00656
F13a1Ratdicoumarol pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00270
F13a1Ratenoxaparin pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00272
F13a1Ratfondaparinux pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00273
F13a1Ratheparin pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00274
F13a1Ratphenindione pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00655
F13a1Ratreteplase pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00285
F13a1Rattranexamic acid pharmacodynamics pathway  ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00287
F13a1Ratwarfarin pharmacodynamics pathway   ISOF13A1 (Homo sapiens)10402751 SMPDBSMP:00268
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Imported Annotations - KEGG (archival)

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F13a1Ratcoagulation cascade pathway   IEA 6907045 KEGGrno:04610
F13a1Ratcomplement system pathway  IEA 6907045 KEGGrno:04610

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#
Reference Title
Reference Citation
1. The Arg703Trp missense mutation in F13A1 is a de novo event. Anwar R and Langlois S, Br J Haematol. 2009 Jun;146(1):118-20. doi: 10.1111/j.1365-2141.2009.07700.x. Epub 2009 Apr 27.
2. Identification of a point mutation in factor XIII A subunit deficiency. Board P, etal., Blood 1992 Aug 15;80(4):937-41.
3. Increased prevalence of microthromboses in retinal capillaries of diabetic individuals. Boeri D, etal., Diabetes. 2001 Jun;50(6):1432-9.
4. Combined carrier status of prothrombin 20210A and factor XIII-A Leu34 alleles as a strong risk factor for myocardial infarction: evidence of a gene-gene interaction. Butt C, etal., Blood. 2003 Apr 15;101(8):3037-41. Epub 2002 Dec 12.
5. Association of a common polymorphism in the factor XIII gene with venous thrombosis. Catto AJ, etal., Blood. 1999 Feb 1;93(3):906-8.
6. Factor XIII Val 34 Leu: a novel association with primary intracerebral hemorrhage. Catto AJ, etal., Stroke. 1998 Apr;29(4):813-6.
7. Factor XIII Val34Leu polymorphism in primary intracerebral haemorrhage. Corral J, etal., Hematol J. 2000;1(4):269-73.
8. Factor XIII improves gastric stress lesions in rats. D'Argenio G, etal., Digestion 2001;63(4):220-8.
9. Genetic polymorphisms associated with priapism in sickle cell disease. Elliott L, etal., Br J Haematol. 2007 May;137(3):262-7.
10. 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.
11. A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): a risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases. Gemmati D, etal., Am J Hematol. 2001 Jul;67(3):183-8.
12. Rat ISS GO annotations from GOA human gene data--August 2006 GOA data from the GO Consortium
13. A common F13A1 intron 1 variant IVS1+12(A) is associated with mild FXIII deficiency in Caucasian population. Ivaskevicius V, etal., Ann Hematol. 2013 Jul;92(7):975-9. doi: 10.1007/s00277-013-1724-2. Epub 2013 Mar 19.
14. Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function. Ivaskevicius V, etal., Haematologica. 2010 Jun;95(6):956-62. doi: 10.3324/haematol.2009.017210. Epub 2010 Feb 23.
15. Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations. Katona E, etal., Haemophilia. 2014 Jan;20(1):114-20. doi: 10.1111/hae.12267. Epub 2013 Oct 1.
16. Leukemic lymphoblasts, a novel expression site of coagulation factor XIII subunit A. Kiss F, etal., Thromb Haemost. 2006 Aug;96(2):176-82.
17. Factor XIII A subunit-deficient mice developed severe uterine bleeding events and subsequent spontaneous miscarriages. Koseki-Kuno S, etal., Blood. 2003 Dec 15;102(13):4410-2. Epub 2003 Aug 21.
18. Role of blood coagulation factor XIII in patients with acute pulmonary embolism. Correlation of factor XIII antigen levels with pulmonary occlusion rate, fibrinogen, D-dimer, and clot firmness. Kucher N, etal., Thromb Haemost. 2003 Sep;90(3):434-8.
19. Targeted inactivation of the mouse locus encoding coagulation factor XIII-A: hemostatic abnormalities in mutant mice and characterization of the coagulation deficit. Lauer P, etal., Thromb Haemost. 2002 Dec;88(6):967-74.
20. Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect. Louhichi N, etal., Ann Hematol. 2010 May;89(5):499-504. doi: 10.1007/s00277-009-0863-y. Epub 2009 Nov 24.
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PMID:8889548   PMID:15507206   PMID:18224415   PMID:22516433   PMID:27363989  



F13a1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81728,021,197 - 28,197,960 (+)NCBIGRCr8
mRatBN7.21727,815,723 - 27,992,494 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1727,815,702 - 27,992,700 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1727,681,035 - 27,857,733 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01729,284,581 - 29,461,269 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01727,645,506 - 27,822,130 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01728,504,650 - 28,680,015 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1728,504,623 - 28,680,362 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01730,406,396 - 30,581,441 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41734,093,525 - 34,270,498 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11734,096,401 - 34,272,682 (+)NCBI
Celera1727,443,244 - 27,619,724 (+)NCBICelera
Cytogenetic Map17p12NCBI
F13A1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3866,144,084 - 6,320,662 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl66,144,084 - 6,321,013 (-)EnsemblGRCh38hg38GRCh38
GRCh3766,144,317 - 6,320,895 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3666,089,310 - 6,265,923 (-)NCBINCBI36Build 36hg18NCBI36
Build 3466,089,316 - 6,265,901NCBI
Celera67,372,733 - 7,550,578 (-)NCBICelera
Cytogenetic Map6p25.1NCBI
HuRef66,020,217 - 6,197,010 (-)NCBIHuRef
CHM1_166,146,854 - 6,323,031 (-)NCBICHM1_1
T2T-CHM13v2.066,013,258 - 6,189,597 (-)NCBIT2T-CHM13v2.0
F13a1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391337,051,150 - 37,234,220 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1337,051,152 - 37,234,220 (-)EnsemblGRCm39 Ensembl
GRCm381336,867,178 - 37,050,244 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1336,867,178 - 37,050,244 (-)EnsemblGRCm38mm10GRCm38
MGSCv371336,959,047 - 37,142,113 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361336,874,653 - 37,056,670 (-)NCBIMGSCv36mm8
Celera1337,983,710 - 38,163,470 (-)NCBICelera
Cytogenetic Map13A3.3NCBI
cM Map1314.44NCBI
F13a1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554657,443,166 - 7,617,436 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554657,444,118 - 7,617,366 (+)NCBIChiLan1.0ChiLan1.0
F13A1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2520,772,261 - 20,960,421 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1616,776,810 - 16,955,131 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v065,978,505 - 6,156,705 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.166,159,012 - 6,337,000 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl66,157,926 - 6,513,961 (-)Ensemblpanpan1.1panPan2
F13A1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1356,186,750 - 6,347,522 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl356,187,235 - 6,349,773 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha356,191,814 - 6,354,808 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0356,267,724 - 6,430,557 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl356,267,724 - 6,428,774 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1356,122,455 - 6,285,137 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0356,148,410 - 6,311,467 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0357,481,872 - 7,644,350 (-)NCBIUU_Cfam_GSD_1.0
F13a1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494617,930,084 - 18,091,733 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365346,199,066 - 6,361,476 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365346,199,066 - 6,360,374 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
F13A1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl73,751,292 - 3,900,762 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.173,751,290 - 3,900,797 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.273,952,957 - 4,102,446 (-)NCBISscrofa10.2Sscrofa10.2susScr3
F13A1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11765,885,498 - 66,040,026 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1765,885,658 - 66,040,040 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660446,090,570 - 6,385,150 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
F13a1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462475619,103,327 - 19,259,964 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462475619,103,064 - 19,259,632 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in F13a1
1025 total Variants

Predicted Target Of
Summary Value
Count of predictions:143
Count of miRNA genes:110
Interacting mature miRNAs:133
Transcripts:ENSRNOT00000021568
Prediction methods:Microtar, Miranda, Pita, 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 39 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
2300002Iddm36Insulin dependent diabetes mellitus QTL 361.98blood glucose amount (VT:0000188)blood glucose level (CMO:0000046)17999128640540197Rat
1354640Scl32Serum cholesterol level QTL 325.4blood HDL cholesterol amount (VT:0000184)blood high density lipoprotein cholesterol level (CMO:0000052)171578159260781592Rat
152023626Bp403Blood pressure QTL 4033.86arterial blood pressure trait (VT:2000000)172393042179524188Rat
1300123Bp194Blood pressure QTL 1942.82arterial blood pressure trait (VT:2000000)mean arterial blood pressure (CMO:0000009)17211514934551001Rat
2302377Scl61Serum cholesterol level QTL 614.36blood HDL cholesterol amount (VT:0000184)serum high density lipoprotein cholesterol level (CMO:0000361)172738994653481766Rat
70157Niddm32Non-insulin dependent diabetes mellitus QTL 324.34blood glucose amount (VT:0000188)blood glucose level area under curve (AUC) (CMO:0000350)172245492450909196Rat
1354651Lmblg2Limb length QTL 26tibia length (VT:0004357)tibia length (CMO:0000450)17429913069599340Rat
1354628Stl13Serum triglyceride level QTL 133.8blood triglyceride amount (VT:0002644)blood triglyceride level (CMO:0000118)172129303960781592Rat
1581512Cm55Cardiac mass QTL 552.80.05heart left ventricle mass (VT:0007031)heart left ventricle weight to body weight ratio (CMO:0000530)172702794956836890Rat

1 to 10 of 39 rows
D17Rat13  
Rat AssemblyChrPosition (strand)SourceJBrowse
GRCr81728,040,628 - 28,040,791 (+)Marker Load Pipeline
mRatBN7.21727,835,154 - 27,835,317 (+)MAPPERmRatBN7.2
Rnor_6.01728,523,806 - 28,523,968NCBIRnor6.0
Rnor_5.01730,425,552 - 30,425,714UniSTSRnor5.0
RGSC_v3.41734,113,131 - 34,113,294RGDRGSC3.4
RGSC_v3.41734,113,132 - 34,113,294UniSTSRGSC3.4
RGSC_v3.11734,115,973 - 34,116,135RGD
Celera1727,462,506 - 27,462,668UniSTS
RH 3.4 Map17353.9RGD
RH 3.4 Map17353.9UniSTS
RH 2.0 Map17236.5RGD
SHRSP x BN Map1721.7599RGD
FHH x ACI Map1728.9299RGD
Cytogenetic Map17p12UniSTS
D17Got41  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21727,921,600 - 27,921,737 (+)MAPPERmRatBN7.2
Rnor_6.01728,609,970 - 28,610,106NCBIRnor6.0
Rnor_5.01730,511,396 - 30,511,532UniSTSRnor5.0
RGSC_v3.41734,199,600 - 34,199,736RGDRGSC3.4
RGSC_v3.41734,199,601 - 34,199,737UniSTSRGSC3.4
RGSC_v3.11734,202,441 - 34,202,577RGD
Celera1727,548,846 - 27,548,982UniSTS
RH 3.4 Map17325.72UniSTS
RH 3.4 Map17325.72RGD
RH 2.0 Map17256.6RGD
Cytogenetic Map17p12UniSTS




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: ENSRNOT00000021568   ⟹   ENSRNOP00000021568
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl1727,815,702 - 27,992,700 (+)Ensembl
Rnor_6.0 Ensembl1728,504,623 - 28,680,362 (+)Ensembl
RefSeq Acc Id: NM_021698   ⟹   NP_067730
RefSeq Status: VALIDATED
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81728,021,197 - 28,197,960 (+)NCBI
mRatBN7.21727,815,723 - 27,992,494 (+)NCBI
Rnor_6.01728,504,650 - 28,680,015 (+)NCBI
Rnor_5.01730,406,396 - 30,581,441 (+)NCBI
RGSC_v3.41734,093,525 - 34,270,498 (+)RGD
Celera1727,443,244 - 27,619,724 (+)RGD
Sequence:
Protein RefSeqs NP_067730 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein CAA73104 (Get FASTA)   NCBI Sequence Viewer  
  EDL98278 (Get FASTA)   NCBI Sequence Viewer  
  EDL98279 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000021568
GenBank Protein O08619 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_067730   ⟸   NM_021698
- UniProtKB: O08619 (UniProtKB/Swiss-Prot),   G3V811 (UniProtKB/TrEMBL),   A6J7C8 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSRNOP00000021568   ⟸   ENSRNOT00000021568
Transglutaminase-like

Name Modeler Protein Id AA Range Protein Structure
AF-O08619-F1-model_v2 AlphaFold O08619 1-732 view protein structure


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

RGD ID:13700399
Promoter ID:EPDNEW_R10922
Type:single initiation site
Name:F13a1_1
Description:coagulation factor XIII A1 chain
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_6.01728,504,629 - 28,504,689EPDNEW


1 to 35 of 35 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-9645 BioCyc
Ensembl Genes ENSRNOG00000015957 Ensembl, ENTREZGENE
Ensembl Transcript ENSRNOT00000021568 ENTREZGENE
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot
  3.90.260.10 UniProtKB/Swiss-Prot
InterPro Ig-like_fold UniProtKB/Swiss-Prot
  Ig_E-set UniProtKB/Swiss-Prot
  Papain-like_cys_pep_sf UniProtKB/Swiss-Prot
  Transglutaminase UniProtKB/Swiss-Prot
  Transglutaminase-like UniProtKB/Swiss-Prot
  Transglutaminase-like_sf UniProtKB/Swiss-Prot
  Transglutaminase_animal UniProtKB/Swiss-Prot
  Transglutaminase_AS UniProtKB/Swiss-Prot
  Transglutaminase_C UniProtKB/Swiss-Prot
  Transglutaminase_C_sf UniProtKB/Swiss-Prot
  Transglutaminase_N UniProtKB/Swiss-Prot
KEGG Report rno:60327 UniProtKB/Swiss-Prot
NCBI Gene 60327 ENTREZGENE
PANTHER PROTEIN-GLUTAMINE GAMMA-GLUTAMYLTRANSFERASE UniProtKB/Swiss-Prot
  PTHR11590:SF42 UniProtKB/Swiss-Prot
Pfam Transglut_C UniProtKB/Swiss-Prot
  Transglut_core UniProtKB/Swiss-Prot
  Transglut_N UniProtKB/Swiss-Prot
PhenoGen F13a1 PhenoGen
PIRSF TGM_EBP42 UniProtKB/Swiss-Prot
PROSITE TRANSGLUTAMINASES UniProtKB/Swiss-Prot
RatGTEx ENSRNOG00000015957 RatGTEx
SMART TGc UniProtKB/Swiss-Prot
Superfamily-SCOP SSF49309 UniProtKB/Swiss-Prot
  SSF54001 UniProtKB/Swiss-Prot
  SSF81296 UniProtKB/Swiss-Prot
UniProt A6J7C8 ENTREZGENE, UniProtKB/TrEMBL
  F13A_RAT UniProtKB/Swiss-Prot
  G3V811 ENTREZGENE, UniProtKB/TrEMBL
  O08619 ENTREZGENE
1 to 35 of 35 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-27 F13a1  coagulation factor XIII A1 chain  F13a1  coagulation factor XIII, A1 polypeptide  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2008-09-09 F13a1  coagulation factor XIII, A1 polypeptide  F13a1  coagulation factor XIII, A1 subunit  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2006-03-30 F13a1  coagulation factor XIII, A1 subunit  F13a    Symbol updated 1299863 APPROVED
2005-01-20 F13a  coagulation factor XIII, A1 subunit    coagulation factor XIIIa  Name updated 1299863 APPROVED
2002-08-07 F13a  coagulation factor XIIIa      Symbol and Name status set to provisional 70820 PROVISIONAL