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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

F10 Gene

protein-coding   GIFtS: 70
GCID: GC13P113777

coagulation factor X

 Explore 104 diseases affiliated with
F10 via our new
 Human Malady Compendium 
Biological research products
for F10
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Coagulation Factor X1 2     Factor Xa2
Stuart-Prower Factor2 3     Prothrombinase1
EC 3.4.21.63 8     Stuart Factor3
FX2     EC 3.4.218
FXA2     

External Ids:    HGNC: 35281   Entrez Gene: 21592   Ensembl: ENSG000001262187   OMIM: 6138725   UniProtKB: P007423   

Export aliases for F10 gene to outside databases

Previous GC identifers: GC13P112387 GC13P108414 GC13P112863 GC13P111725 GC13P112825 GC13P094215


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for F10:
This gene encodes the vitamin K-dependent coagulation factor X of the blood coagulation cascade. This factor undergoes
multiple processing steps before its preproprotein is converted to a mature two-chain form by the excision of the
tripeptide RKR. Two chains of the factor are held together by 1 or more disulfide bonds; the light chain contains 2
EGF-like domains, while the heavy chain contains the catalytic domain which is structurally homologous to those of the
other hemostatic serine proteases. The mature factor is activated by the cleavage of the activation peptide by factor
IXa (in the intrisic pathway), or by factor VIIa (in the extrinsic pathway). The activated factor then converts
prothrombin to thrombin in the presence of factor Va, Ca+2, and phospholipid during blood clotting. Mutations of this
gene result in factor X deficiency, a hemorrhagic condition of variable severity. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: FA10_HUMAN, P00742
Function: Factor Xa is a vitamin K-dependent glycoprotein that converts prothrombin to thrombin in the presence of
factor Va, calcium and phospholipid during blood clotting

Gene Wiki entry for F10 (Factor X)


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000013.10  NC_018924.1  NT_027140.6  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the F10 gene promoter:
         E2F-4   c-Fos   E2F-1   E2F   AP-1   ATF-2   c-Jun   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidF10 promoter sequence
   Search SABiosciences Chromatin IP Primers for F10

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat F10


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 13q34   Ensembl cytogenetic band:  13q34   HGNC cytogenetic band: 13q34

F10 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
F10 gene location

GeneLoc information about chromosome 13         GeneLoc Exon Structure

GeneLoc location for GC13P113777:  view genomic region     (about GC identifiers)

Start:
113,777,113 bp from pter      End:
113,803,843 bp from pter
Size:
26,731 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: FA10_HUMAN, P00742 (See protein sequence)
Recommended Name: Coagulation factor X precursor  
Size: 488 amino acids; 54732 Da
Subunit: The two chains are formed from a single-chain precursor by the excision of two Arg residues and are held
together by 1 or more disulfide bonds. Forms a heterodimer with SERPINA5
Subcellular location: Secreted
6/125 PDB 3D structures from and Proteopedia for F10 (see all 125):
1C5M (3D)        1EZQ (3D)        1F0R (3D)        1F0S (3D)        1FAX (3D)        1FJS (3D)    
Secondary accessions: Q14340

Explore the universe of human proteins at neXtProt for F10: NX_P00742

Post-translational modifications:

  • The vitamin K-dependent, enzymatic carboxylation of some glutamate residues allows the modified protein to bind calcium1
  • N- and O-glycosylated. O-glycosylated with core 1 or possibly core 8 glycans1
  • The activation peptide is cleaved by factor IXa (in the intrinsic pathway), or by factor VIIa (in the extrinsic
  • pathway)1
  • The iron and 2-oxoglutarate dependent 3-hydroxylation of aspartate and asparagine is (R) stereospecific within EGF
  • domains1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P00742

  • 4/13 DME Specific Peptides for F10 (P00742) (see all 13)
     FCGGTIL  GECPWQA  SWGEGCA  TGIVSWG 

    F10 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_000495.1  
    ENSEMBL proteins: 
     ENSP00000387092   ENSP00000364701   ENSP00000364709   ENSP00000386320  
    Reactome Protein details: P00742
    Human Recombinant Protein Products: 
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    Uscn Proteins for F10

    Gene Ontology (GO): 5/7 cellular component terms (GO ID links to tree view) (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005576extracellular region TAS--
    GO:0005624membrane fraction ----
    GO:0005788endoplasmic reticulum lumen TAS--
    GO:0005792microsome ----
    GO:0005796Golgi lumen TAS--


    F10 for ontologies           About GeneDecksing



    F10 Antibody Products: 
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    Uscn ELISAs and CLIAs for F10


    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    F10 for domains           About GeneDecksing

    5/12 InterPro domains/families (see all 12):
     IPR017857 Coagulation_fac_subgr_Gla_dom
     IPR001314 Peptidase_S1A
     IPR000742 EG-like_dom
     IPR000152 EGF-type_Asp/Asn_hydroxyl_site
     IPR018097 EGF_Ca-bd_CS

    Graphical View of Domain Structure for InterPro Entry P00742

    ProtoNet protein and cluster: P00742

    5/7 Blocks protein families (see all 7):
    IPB000152 Aspartic acid and asparagine hydroxylation site
    IPB000294 Vitamin K-dependent carboxylation/gamma-carboxyglutamic (GLA) domain
    IPB001254 Serine protease
    IPB001314 Chymotrypsin serine protease family (S1) signature
    IPB001438 Type II EGF-like signature


    UniProtKB/Swiss-Prot: FA10_HUMAN, P00742
    Similarity: Belongs to the peptidase S1 family
    Similarity: Contains 2 EGF-like domains
    Similarity: Contains 1 Gla (gamma-carboxy-glutamate) domain
    Similarity: Contains 1 peptidase S1 domain


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: FA10_HUMAN, P00742
    Function: Factor Xa is a vitamin K-dependent glycoprotein that converts prothrombin to thrombin in the presence of
    factor Va, calcium and phospholipid during blood clotting
    Catalytic activity: Selective cleavage of Arg- -Thr and then Arg- -Ile bonds in prothrombin to form thrombin
    Enzyme regulation: Inhibited by SERPINA5 and SERPINA10

         Genatlas biochemistry entry for F10:
    coagulation factor X (Stuart Prower),vitamin K-dependent

    Enzyme Numbers (IUBMB): EC 3.4.21.61 2 EC 3.4.212

    miRNA
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    Browse SwitchGear 3'UTR luciferase reporter plasmids
    Inhib. RNA
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    OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for F10 (see all 7)
    OriGene shRNA RFP: F10
    OriGene siRNA: F10
    QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat F10

    Gene Editing
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    Clone
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    OriGene custom cloning services – gene synthesis, subcloning, mutagenesis, variant library, vector shuttling 
    GenScript: all cDNA clones in your preferred vector: F10 (NM_014206)
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    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat F10 

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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for F10

    Gene Ontology (GO): 4 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0004252serine-type endopeptidase activity TAS--
    GO:0005509calcium ion binding IEA--
    GO:0005515protein binding IPI6323392
    GO:0005543phospholipid binding IDA17469850


    F10 for ontologies           About GeneDecksing


    Animal Models:
         Mouse knock-outs for F10: F10tm1Ccmt F10tm1Edr
         4 MGI mutant phenotypes (inferred from 3 alleles(MGI details for F10):
     cardiovascular system  homeostasis/metabolism  mortality/aging  reproductive system 

    F10 for phenotypes           About GeneDecksing


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section

    Unified GeneCards pathways - 5/8 super-pathways (see all 8About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Gamma-carboxylation, transport, and amino-terminal cleavage of proteins
    Gamma-carboxylation, transport, and amino-terminal cleavage of proteins1.00
    Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus0.73
    Removal of aminoterminal propeptides from gamma-carboxylated proteins0.82
    Warfarin Pathway, Pharmacodynamics0.67
    Gamma-carboxylation of protein precursors0.82
    Extrinsic Pathway0.23
    2Formation of Fibrin Clot (Clotting Cascade)
    Formation of Fibrin Clot (Clotting Cascade)1.00
    Blood Coagulation Signaling Pathways0.51
    Intrinsic Pathway0.59
    Blood Clotting Cascade0.36
    3Blood Coagulation Cascade
    Blood Coagulation Cascade1.00
    Intrinsic Prothrombin Activation Pathway0.96
    4Complement and coagulation cascades
    Complement and coagulation cascades1.00
    Complement and Coagulation Cascades0.72
    5Common Pathway
    Common Pathway1.00
    Extrinsic Prothrombin Activation Pathway0.69

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    1 R&D Systems Pathway for F10
        Blood Coagulation Signaling Pathways

    3 Downloadable PowerPoint Slides of QIAGEN Pathway Central Maps for F10
        Extrinsic Prothrombin Activation Pathway
    Blood Coagulation Cascade
    Intrinsic Prothrombin Activation Pathway

    2 BioSystems Pathways for F10 
        Blood Clotting Cascade
    Complement and Coagulation Cascades

    5/12        Reactome Pathways for F10 (see all 12)
        Hemostasis
    Extrinsic Pathway
    Intrinsic Pathway
    Removal of aminoterminal propeptides from gamma-carboxylated proteins
    Common Pathway

    1 PharmGKB Pathway for F10
        Warfarin Pathway, Pharmacodynamics

    1         Kegg Pathway  (Kegg details for F10):
        Complement and coagulation cascades


    F10 for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for F10

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/35 Interacting proteins for F10 (P007422, 3 ENSP000003647094) via UniProtKB, MINT, STRING, and/or I2D (see all 35)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    MGST3O148803, ENSP000003568594I2D: score=3 STRING: ENSP00000356859
    F5P122593, ENSP000003567714I2D: score=2 STRING: ENSP00000356771
    F7P087093, ENSP000003647314I2D: score=2 STRING: ENSP00000364731
    F8P004513, ENSP000003533934I2D: score=2 STRING: ENSP00000353393
    HIST1H1CP164033, ENSP000003395664I2D: score=2 STRING: ENSP00000339566
    About this table

    Gene Ontology (GO): 5/9 biological process terms (GO ID links to tree view) (see all 9):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006508proteolysis TAS--
    GO:0007596blood coagulation TAS--
    GO:0007597blood coagulation, intrinsic pathway TAS--
    GO:0007598blood coagulation, extrinsic pathway TAS--
    GO:0017187peptidyl-glutamic acid carboxylation TAS--


    F10 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    F10 for compounds           About GeneDecksing

    EMD Millipore small molecules for F10:
    Small Molecule - inhibitor
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for F10

    2 HMDB Compounds for F10    About this table
    CompoundSynonyms CAS #PubMed Ids
    CalciumCa (see all 2)7440-70-2--
    MenadioneVitamin K3: 1,4-Dihydro-1,4-dioxo-2-methylnaphthalene (see all 49)58-27-5--

    10/38 DrugBank Compounds for F10 (see all 38)    About this table
    CompoundSynonyms CAS #TypeActionsPubMed Ids
    Coagulation Factor IXChristmas factor (see all 4)9001-28-9targetactivator1391956 659613 9079657 11752352 8083242 10919405 10933803
    Antihemophilic FactorAHF (see all 3)--targetactivator14285227 6436416 236567 11891806 13801371
    Coagulation factor VIIaCoagulation factor VII precursor (see all 5)9001-25-6target--5969560 13713641 14227143 13621053 13801371
    EnoxaparinLMWH (see all 2)9005-49-6targetinhibitor17567541 17474542 16187968 17509040 15675440
    HeparinAlpha-Heparin (see all 8)9005-49-6targetinhibitor17004727 17118432 3155697 11369259
    Menadione2-Methyl-1,4-Naphthalenedione (see all 7)58-27-5targetactivator17139284 17016423
    Rivaroxaban-- 366789-02-8targetantagonist20135071 20424181
    (2R)-2-(5-CHLORO-2-THIENYL)-N-{(3S)-1-[(1S)-1-METHYL-2-MORPHOLIN-4-YL-2-OXOETHYL]-2-OXOPYRROLIDIN-3-YL}PROPENE-1-SULFONAMIDE-- --target--10592235
    (2R,4R)-N~1~-(4-CHLOROPHENYL)-N~2~-[2-FLUORO-4-(2-OXOPYRIDIN-1(2H)-YL)PHENYL]-4-METHOXYPYRROLIDINE-1,2-DICARBOXAMIDE-- --target--10592235
    1-[[(1E)-2-(4-CHLOROPHENYL)ETHENYL]SULFONYL]-4-[[1-(4-PYRIDINYL)-4-PIPERIDINYL]METHYL]PIPERAZINE-- --target--10592235

    10/115 Novoseek chemical compound relationships for F10 gene (see all 115)    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    rivaroxaban 94.4 125 17938768 (3), 18307374 (3), 20139357 (3), 17595891 (3) (see all 77)
    fondaparinux 94.3 179 12871328 (3), 15744699 (3), 15171960 (2), 12501872 (2) (see all 99)
    apixaban 91.7 42 19851712 (5), 18315548 (3), 17868430 (2), 18393142 (1) (see all 29)
    heparin 88.8 634 12871328 (6), 11009624 (5), 9642241 (5), 19967150 (5) (see all 99)
    heparin pentasaccharide 88.6 11 12353073 (2), 11854268 (1), 14532267 (1), 12871328 (1) (see all 8)
    dabigatran etexilate 86.4 16 19601856 (1), 19550318 (1), 18473863 (1), 19803538 (1) (see all 13)
    otamixaban 83 12 17139573 (3), 17178269 (2), 16493482 (2), 19717184 (1) (see all 8)
    hirudin 82.4 65 12883328 (3), 7740455 (3), 8218854 (2), 2096492 (2) (see all 42)
    antistasin 82.1 23 7740449 (2), 9804761 (2), 8218854 (2), 1990979 (2) (see all 12)
    gamma-carboxyglutamic acid 81.4 47 8226763 (4), 17387172 (3), 9780208 (2), 8355279 (1) (see all 19)

    Search CenterWatch for drugs/clinical trials and news about F10 / FA10 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for F10 gene: 
    NM_000504.3  

    Unigene Cluster for F10:

    Coagulation factor X
    Hs.361463  [show with all ESTs]
    Unigene Representative Sequence: BC040125
    7 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000409306 ENST00000375551(uc001vsy.3) ENST00000375559(uc001vsx.3)
    ENST00000477269 ENST00000483537 ENST00000410083(uc010agq.1) ENST00000498455


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    Clone
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    GenScript: all cDNA clones in your preferred vector: F10 (NM_014206)
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      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat F10

    Additional cDNA sequence: 

    AK310772.1 AK310775.1 AK313798.1 BC040125.1 BC046125.1 K01886.1 K03194.1 M22613.1 
    M57285.1 

    8 DOTS entries:

    DT.313355  DT.97856616  DT.100676340  DT.97861708  DT.120640635  DT.120780844  DT.97781688  DT.121305757 

    24/72 AceView cDNA sequences (see all 72):

    CR607773 CD518821 BQ018853 CD014138 CA444781 CB162539 CB158437 BU846186 
    BQ027447 CR623031 BM709916 BP339855 NM_000504 M22613 BC046125 M57285 
    BU849949 BC040125 K01886 CD013940 CR603372 CD676150 BM987312 AL576464 

    GeneLoc Exon Structure

    5/6 Alternative Splicing Database (ASD) splice patterns (SP) for F10 (see all 6)    About this scheme

    ExUns: 1a · 1b · 1c ^ 2 ^ 3 ^ 4 ^ 5 ^ 6a · 6b ^ 7a · 7b ^ 8a · 8b · 8c ^ 9a · 9b · 9c
    SP1:                          -                 -                 -                                       
    SP2:                          -                 -     -           -                                       
    SP3:                          -                 -                                                         
    SP4:                                            -                 -                 -                     
    SP5:                                                              -                                       


    ECgene alternative splicing isoforms for F10

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    F10 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: CCCCGGAGGT

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image

    F10 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    3 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    HeartCardiac CrescentCardiac Crescent CellsMyocardium
    OvaryPrimary FollicleGranulosa CellsOvary
    Yolk SacDefinitive Yolk SacDefinitive Hematopoietic Stem CellsBlood
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 4 LifeMap Cells 
    NameCategory
    PureStem™ progenitor EN7 (Embryonic Progenitor Cell)
    PureStem™ progenitor W10 (Embryonic Progenitor Cell)
    Definitive endoderm-like cells (Generation and expan...)
    Endoderm progenitor-like cells (Generation and expan...)

    See F10 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for F10

    SOURCE GeneReport for Unigene cluster: Hs.361463

    UniProtKB/Swiss-Prot: FA10_HUMAN, P00742
    Tissue specificity: Plasma; synthesized in the liver

        SABiosciences Expression via Pathway-Focused PCR Array including F10: 
              Hypoxia Signaling Pathway in human mouse rat

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    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of animals.

    Orthologs for F10 gene from 5/16 species (see all 16)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves F101 coagulation factor X 59.8(n)
    57.3(a)
      395876  NM_205022.1  NP_990353.1 
    lizard
    (Anolis carolinensis)
    Reptilia F106
    --
    46(a)
    1 ↔ 1
    3(105959705-105966831)
    African clawed frog
    (Xenopus laevis)
    Amphibia MGC684542 hypothetical protein MGC68454 74.97(n)    BC060330.1 
    zebrafish
    (Danio rerio)
    Actinopterygii f102 coagulation factor X 74.88(n)   282670  BC056804.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG118361 , 3 serine-type endopeptidase3
    CG118361
    39(a)3
    48.92(n)1
    39.83(a)1
      96B203
    430071  NM_001170247.31  NP_001163718.31 


    ENSEMBL Gene Tree for F10 (if available)
    TreeFam Gene Tree for F10 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for F10 gene
    PROZ2  PAMR12  C1S2  C1R2  C1RL2  F92  MASP12  F22  
    HPR2  HP2  PROC2  F72  MASP22  
    15 SIMAP similar genes for F10 using alignment to 6 protein entries:     FA10_HUMAN (see all proteins):
    PRRG1    PROS1    PRRG3    PROC1    F9    KLK4
    F9 p22    PRSS1    factor IX F9    F2    PRSS2    TRY8
    F7    PROC    KLK9

    F10 for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/620 NCBI SNPs in F10 are shown (see all 620    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 13 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs617532661,2
    C,F,pathogenic94233671(+) GCCACG/AAGGAA 2 /K /E mis11Minor allele frequency- A:0.00NA 4552
    rs1048943921,2
    Cpathogenic94241845(+) TCGGGC/TGCACC 2 R C mis10--------
    rs792756681,2
    C,--94214234(+) CCAGAA/CCCACA 1 -- us2k10--------
    rs30932681,2
    C,F,--94214362(+) CAGAGG/CCTTCG 1 -- us2k1 tfbs312Minor allele frequency- C:0.03NS NA WA 2438
    rs32117081,2
    H--94214377(+) AGGGCC/TTGGGC 1 -- us2k16Minor allele frequency- T:0.00NS EA 494
    rs32129901,2
    C,F,H,--94214580(+) GCCATG/AAGCAT 1 -- us2k110Minor allele frequency- A:0.01NS EA NA 676
    rs797930991,2
    C,F,--94214788(+) CAGTCG/AGGTGG 1 -- us2k11Minor allele frequency- A:0.02WA 118
    rs32117101,2
    H--94214881(+) CAGGGC/TGACCC 1 -- us2k16Minor allele frequency- T:0.00NS EA 514
    rs4746711,2
    C,F,--94214923(+) AGTGCT/CGTGGG 1 -- us2k121Minor allele frequency- C:0.14EA NA NS WA CSA 1307
    rs32117121,2
    C,F,H,--94215061(+) CACAGC/GCATTG 1 -- us2k17Minor allele frequency- G:0.02NS EA NA 358

    HapMap Linkage Disequilibrium report for F10 (113777113 - 113803843 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 7 variations for F10
         5 CNVs: 76521 9723 4819 87067 87068
         2 Indels: 87069 25168
    Human Gene Mutation Database (HGMD): F10

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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    F10 for disorders           About GeneDecksing

    OMIM gene information: 613872    OMIM disorders: --

    UniProtKB/Swiss-Prot: FA10_HUMAN, P00742
  • Defects in F10 are the cause of factor X deficiency (FA10D) [MIM:227600]. A hemorrhagic disease with variable
  • presentation. Affected individuals can manifest prolonged nasal and mucosal hemorrhage, menorrhagia, hematuria, and
    occasionally hemarthrosis. Some patients do not have clinical bleeding diathesis

    20/104 diseases for F10 (see all 104):    About MalaCards
    factor x deficiency    vitamin k-dependent clotting factors    disseminated intravascular coagulation    antithrombin iii deficiency
    quebec platelet disorder    factor vii deficiency    heparin-induced thrombocytopenia    deep vein thrombosis
    glanzmann's thrombasthenia    paroxysmal nocturnal hemoglobinuria    dysprothrombinemia    west nile virus
    beta thalassemia    hemophilia    intermittent claudication    carotid artery thrombosis
    hemarthrosis    pre-eclampsia    myocardial infarction    atrial fibrillation

    4 diseases from the University of Copenhagen DISEASES database for F10:
    Carney complex     Pulmonary embolism     Factor X deficiency     Disseminated intravascular coagulation

    10/85 Novoseek disease relationships for F10 gene (see all 85)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    factor x deficiency 81 3 9799000 (1), 8449937 (1), 15569527 (1)
    thromboembolism 80.6 54 16409461 (2), 19485937 (2), 16241946 (2), 14650860 (2) (see all 44)
    scott syndrome 76.1 5 1730083 (2), 9054648 (1), 19408196 (1), 11421293 (1)
    thrombosis 76 71 10604970 (2), 11554940 (2), 12829728 (2), 15338955 (2) (see all 54)
    deep vein thrombosis 71.1 8 15091002 (1), 15554723 (1), 8029801 (1), 12750119 (1) (see all 8)
    arterial thrombosis 69.2 17 10813384 (1), 11177336 (1), 11342132 (1), 17729190 (1) (see all 14)
    bleeding 67.9 53 11554940 (2), 19598069 (2), 12829728 (2), 14633255 (2) (see all 44)
    venous thrombosis 62.8 25 11434677 (3), 9241747 (2), 9336303 (1), 10813384 (1) (see all 14)
    coagulopathy 62.1 15 11554940 (2), 19598069 (2), 14995986 (1), 12161341 (1) (see all 11)
    hemophilia a 60.9 3 2130929 (1), 14717973 (1), 16409469 (1)

    Genatlas disease: F10
    bleeding diathesis (FX deficiency)

    Human Genome Epidemiology (HuGE) Navigator: F10 (17 documents)

    Export disorders for F10 gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for F10 gene, integrated from 9 sources (see all 1571):
    (articles sorted by number of sources associating them with F10)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X. (PubMed id 19135706)1, 2, 9 Chafa O....Lebonniec B.F. (2009)
    2. Activation-dependent exposure of the inter-EGF sequence Leu83-Leu88 in factor Xa mediates ligand binding to effector cell protease receptor-1. (PubMed id 9079657)1, 7, 9 Ambrosini G....Altieri D.C. (1997)
    3. Monitoring Unfractionated Heparin (UFH) therapy: which Anti-Factor Xa assay is appropriate? (PubMed id 17118432)1, 7, 9 Ignjatovic V....Monagle P. (2007)
    4. Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly. (PubMed id 17393015)1, 2, 9 Al-Hilali A....Herrmann F.H. (2007)
    5. Structural basis for chemical inhibition of human blood coagulation factor Xa. (PubMed id 9618463)1, 2, 9 Kamata K.... Kim S.H. (1998)
    6. Structure of human des(1-45) factor Xa at 2.2-A resolution. (PubMed id 8355279)1, 2, 9 Padmanabhan K.... Kisiel W. (1993)
    7. Cloning and expression in COS-1 cells of a full-length cDNA encoding human coagulation factor X. (PubMed id 1902434)1, 2, 9 Messier T.L.... Church W.R. (1991)
    8. Basis for the specificity and activation of the serpi n protein Z-dependent proteinase inhibitor (ZPI) as an inhibitor of membrane-as sociated factor Xa. (PubMed id 20427285)1, 2 Huang X....Gettins P.G. (2010)
    9. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    10. Molecular analysis of the genotype-phenotype relationship in factor X deficiency. (PubMed id 10746568)1, 2 Millar D.S....Cooper D.N. (2000)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 2159 HGNC: 3528 AceView: F10 Ensembl:ENSG00000126218 euGenes: HUgn2159
    ECgene: F10 Kegg: 2159 H-InvDB: F10

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for F10 Pharmacogenomics, SNPs, Pathways
    Wikipedia http://en.wikipedia.org/wiki/Factor_X
    SeattleSNPshttp://pga.gs.washington.edu/data/f10/

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for F10 gene:
    Search GeneIP for patents involving F10

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



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