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    F13A1 coagulation factor XIII A chain [ Homo sapiens (human) ]

    Gene ID: 2162, updated on 16-Aug-2021

    Summary

    Official Symbol
    F13A1provided by HGNC
    Official Full Name
    coagulation factor XIII A chainprovided by HGNC
    Primary source
    HGNC:HGNC:3531
    See related
    Ensembl:ENSG00000124491 MIM:134570
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    F13A
    Summary
    This gene encodes the coagulation factor XIII A subunit. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have enzymatic activity and may serve as plasma carrier molecules. Platelet factor XIII is comprised only of 2 A subunits, which are identical to those of plasma origin. Upon cleavage of the activation peptide by thrombin and in the presence of calcium ion, the plasma factor XIII dissociates its B subunits and yields the same active enzyme, factor XIIIa, as platelet factor XIII. This enzyme acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinking between fibrin molecules, thus stabilizing the fibrin clot. It also crosslinks alpha-2-plasmin inhibitor, or fibronectin, to the alpha chains of fibrin. Factor XIII deficiency is classified into two categories: type I deficiency, characterized by the lack of both the A and B subunits; and type II deficiency, characterized by the lack of the A subunit alone. These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion. [provided by RefSeq, Jul 2008]
    Expression
    Biased expression in placenta (RPKM 246.8), urinary bladder (RPKM 65.1) and 12 other tissues See more
    Orthologs
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    Genomic context

    See F13A1 in Genome Data Viewer
    Location:
    6p25.1
    Exon count:
    15
    Annotation release Status Assembly Chr Location
    109.20210514 current GRCh38.p13 (GCF_000001405.39) 6 NC_000006.12 (6144084..6320662, complement)
    105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (6144317..6320895, complement)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105374898 Neighboring gene pyruvate kinase M1/2 pseudogene 5 Neighboring gene neuritin 1 Neighboring gene microRNA 7853 Neighboring gene microRNA 5683 Neighboring gene LY86 antisense RNA 1 Neighboring gene small nuclear RNA activating complex polypeptide 5 pseudogene 1 Neighboring gene calponin 3 pseudogene 1

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    Associated conditions

    Description Tests
    Factor XIII, A subunit, deficiency of
    MedGen: C2750514 OMIM: 613225 GeneReviews: Not available
    Compare labs
    Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.
    GeneReviews: Not available
    Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.
    GeneReviews: Not available
    Ischemic stroke is associated with the ABO locus: the EuroCLOT study.
    GeneReviews: Not available
    Myocardial infarction 1
    MedGen: C1832662 OMIM: 608446 GeneReviews: Not available
    Compare labs
    Thrombophilia due to thrombin defect
    MedGen: C3160733 OMIM: 188050 GeneReviews: Prothrombin Thrombophilia
    Compare labs

    HIV-1 interactions

    Protein interactions

    Protein Gene Interaction Pubs
    Tat tat Microarray analysis indicates HIV-1 Tat-induced downregulation of coagulation factor XIII, A1 polypeptide (F13A1) in primary human brain microvascular endothelial cells PubMed

    Go to the HIV-1, Human Interaction Database

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Homology

    General protein information

    Preferred Names
    coagulation factor XIII A chain
    Names
    FSF, A subunit
    TGase
    bA525O21.1 (coagulation factor XIII, A1 polypeptide)
    coagulation factor XIII, A polypeptide
    coagulation factor XIII, A1 polypeptide
    coagulation factor XIIIa
    factor XIIIa
    fibrin stabilizing factor, A subunit
    fibrinoligase
    protein-glutamine gamma-glutamyltransferase A chain
    transglutaminase A chain
    transglutaminase. plasma
    NP_000120.2

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_008107.1 RefSeqGene

      Range
      5001..181614
      Download
      GenBank, FASTA, Sequence Viewer (Graphics), LRG_549

    mRNA and Protein(s)

    1. NM_000129.4NP_000120.2  coagulation factor XIII A chain

      See identical proteins and their annotated locations for NP_000120.2

      Status: REVIEWED

      Source sequence(s)
      AB208852, AL157775, BP251770
      Consensus CDS
      CCDS4496.1
      UniProtKB/Swiss-Prot
      P00488
      Related
      ENSP00000264870.3, ENST00000264870.8
      Conserved Domains (4) summary
      smart00460
      Location:309400
      TGc; Transglutaminase/protease-like homologues
      COG1305
      Location:284408
      YebA; Transglutaminase-like enzyme, putative cysteine protease [Posttranslational modification, protein turnover, chaperones]
      pfam00868
      Location:47164
      Transglut_N; Transglutaminase family
      pfam00927
      Location:519623
      Transglut_C; Transglutaminase family, C-terminal ig like domain

    RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000006.12 Reference GRCh38.p13 Primary Assembly

      Range
      6144084..6320662 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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