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    KNG1 kininogen 1 [ Homo sapiens (human) ]

    Gene ID: 3827, updated on 10-Dec-2024

    Summary

    Official Symbol
    KNG1provided by HGNC
    Official Full Name
    kininogen 1provided by HGNC
    Primary source
    HGNC:HGNC:6383
    See related
    Ensembl:ENSG00000113889 MIM:612358; AllianceGenome:HGNC:6383
    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
    BK; HK; BDK; KNG; HAE6; HMWK
    Summary
    This gene uses alternative splicing to generate two different proteins- high molecular weight kininogen (HMWK) and low molecular weight kininogen (LMWK). HMWK is essential for blood coagulation and assembly of the kallikrein-kinin system. Also, bradykinin, a peptide causing numerous physiological effects, is released from HMWK. Bradykinin also functions as an antimicrobial peptide with antibacterial and antifungal activity. In contrast to HMWK, LMWK is not involved in blood coagulation. Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) reduces or depletes angiotensin converting enzyme 2 (ACE2), which results in an increase in levels of des-Arg(9)-bradykinin, a bioactive metabolite of bradykinin that is associated with lung injury and inflammation. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2020]
    Annotation information
    Note: This gene has been reviewed for its involvement in coronavirus biology, and is relevant for disease process.
    Expression
    Restricted expression toward liver (RPKM 432.8) See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See KNG1 in Genome Data Viewer
    Location:
    3q27.3
    Exon count:
    10
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (186717359..186744410)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (189539122..189566165)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (186435148..186462199)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene HRG pseudogene 1 Neighboring gene HRG pseudogene 2 Neighboring gene NANOG hESC enhancer GRCh37_chr3:186442598-186443161 Neighboring gene proteasome 26S subunit, non-ATPase, 10 pseudogene 2 Neighboring gene RNA, U6 small nuclear 1105, pseudogene

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    Associated conditions

    Description Tests
    Angioedema, hereditary, 6
    MedGen: C5543516 OMIM: 619363 GeneReviews: Not available
    Compare labs
    High molecular weight kininogen deficiency
    MedGen: C0272340 OMIM: 228960 GeneReviews: Not available
    Compare labs

    EBI GWAS Catalog

    Description
    An atlas of genetic influences on human blood metabolites.
    EBI GWAS Catalog
    Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.
    EBI GWAS Catalog
    Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.
    EBI GWAS Catalog
    Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ.
    EBI GWAS Catalog

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables cysteine-type endopeptidase inhibitor activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables cysteine-type endopeptidase inhibitor activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables heparin binding NAS
    Non-traceable Author Statement
    more info
    PubMed 
    enables hormone activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables signaling receptor binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables zinc ion binding NAS
    Non-traceable Author Statement
    more info
    PubMed 

    General protein information

    Preferred Names
    kininogen-1
    Names
    alpha-2-thiol proteinase inhibitor
    bradykinin
    fitzgerald factor
    high molecular weight kininogen
    williams-Fitzgerald-Flaujeac factor

    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_016009.1 RefSeqGene

      Range
      5051..32102
      Download
      GenBank, FASTA, Sequence Viewer (Graphics), LRG_598

    mRNA and Protein(s)

    1. NM_000893.4NP_000884.1  kininogen-1 isoform 2 precursor

      See identical proteins and their annotated locations for NP_000884.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) uses an alternate splice pattern in the 3' coding region, compared to variant 1. The resulting isoform (2), also known as low molecular weight preprokininogen, has a shorter and distinct C-terminus, compared to isoform 1.
      Source sequence(s)
      AC109780, AC112907, DC362362, K02566
      Consensus CDS
      CCDS3281.1
      UniProtKB/TrEMBL
      B4DPP8, E9PEA0
      Related
      ENSP00000287611.2, ENST00000287611.8
      Conserved Domains (1) summary
      pfam00031
      Location:266360
      Cystatin; Cystatin domain
    2. NM_001102416.3NP_001095886.1  kininogen-1 isoform 1 precursor

      See identical proteins and their annotated locations for NP_001095886.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1), also known as high molecular weight preprokininogen.
      Source sequence(s)
      AC109780, AC112907, DC362362, K02566
      Consensus CDS
      CCDS43183.1
      UniProtKB/Swiss-Prot
      A8K474, B2RCR2, C9JEX1, P01042, P01043, Q53EQ0, Q6PAU9, Q7M4P1
      UniProtKB/TrEMBL
      B4E1C2
      Related
      ENSP00000493985.1, ENST00000644859.2
      Conserved Domains (1) summary
      cd00042
      Location:266370
      CY; Cystatin-like domain; Cystatins are a family of cysteine protease inhibitors that occur mainly as single domain proteins. However some extracellular proteins such as kininogen, His-rich glycoprotein and fetuin also contain these domains.
    3. NM_001166451.2NP_001159923.1  kininogen-1 isoform 3 precursor

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) uses an alternate splice pattern in the 3' coding region and lacks an alternate in-frame exon, compared to variant 1. The resulting isoform (3) has a shorter and distinct C-terminus and lacks an internal segment, compared to isoform 1.
      Source sequence(s)
      AC112907, CD014130
      Consensus CDS
      CCDS54695.1
      UniProtKB/TrEMBL
      B4DPP8, E9PEA0
      Related
      ENSP00000396025.1, ENST00000447445.1
      Conserved Domains (1) summary
      pfam00031
      Location:230324
      Cystatin; Cystatin domain

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

      Range
      186717359..186744410
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060927.1 Alternate T2T-CHM13v2.0

      Range
      189539122..189566165
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)