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    PTX4 pentraxin 4 [ Homo sapiens (human) ]

    Gene ID: 390667, updated on 10-Dec-2024

    Summary

    Official Symbol
    PTX4provided by HGNC
    Official Full Name
    pentraxin 4provided by HGNC
    Primary source
    HGNC:HGNC:14171
    See related
    Ensembl:ENSG00000251692 MIM:613442; AllianceGenome:HGNC:14171
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    C16orf38
    Summary
    This gene belongs to the pentraxin superfamily, whose members encode highly conserved multifunctional proteins. The encoded protein, like other members of this family, contains a conserved pentraxin domain at the C-terminus. The highest levels of expression of the protein were observed in bone marrow, small intestine and testes. [provided by RefSeq, Jun 2016]
    Expression
    Low expression observed in reference dataset See more
    Orthologs
    NEW
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    Genomic context

    See PTX4 in Genome Data Viewer
    Location:
    16p13.3
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (1485886..1488944, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (1500922..1503980, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (1535887..1538945, complement)

    Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene chloride voltage-gated channel 7 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6986 Neighboring gene H3K27ac hESC enhancer GRCh37_chr16:1524989-1525532 Neighboring gene ReSE screen-validated silencer GRCh37_chr16:1534269-1534471 Neighboring gene RPS3A pseudogene 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 10226 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1543166-1544066 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1544968-1545868 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1545869-1546768 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_42864 Neighboring gene telomere maintenance 2 Neighboring gene intraflagellar transport 140 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr16:1574508-1575707 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1582993-1583696 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1583697-1584400 Neighboring gene transmembrane protein 204 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr16:1592422-1593124 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr16:1605115-1605614

    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

    Phenotypes

    EBI GWAS Catalog

    Description
    Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General protein information

    Preferred Names
    pentraxin-4
    Names
    long pentraxin 4
    neuronal pentraxin-like protein C16orf38
    pentraxin 4, long

    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.

    mRNA and Protein(s)

    1. NM_001013658.1NP_001013680.1  pentraxin-4 isoform 2

      See identical proteins and their annotated locations for NP_001013680.1

      Status: VALIDATED

      Description
      Transcript Variant: This transcript (2) uses an alternate 5' terminal exon and an alternate start codon, compared to variant 1. It encodes isoform 2, which has a shorter and distinct N-terminus, compared to isoform 1.
      Source sequence(s)
      AE006467
      Consensus CDS
      CCDS32362.1
      UniProtKB/Swiss-Prot
      Q96A99
      Related
      ENSP00000293922.1, ENST00000293922.1
      Conserved Domains (1) summary
      cd00152
      Location:265462
      PTX; Pentraxins are plasma proteins characterized by their pentameric discoid assembly and their Ca2+ dependent ligand binding, such as Serum amyloid P component (SAP) and C-reactive Protein (CRP), which are cytokine-inducible acute-phase proteins implicated ...
    2. NM_001328608.2NP_001315537.1  pentraxin-4 isoform 1 precursor

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) encodes the longer isoform (1). This transcript is based on data in PMID:20357257.
      Source sequence(s)
      AL031705
      Consensus CDS
      CCDS86492.1
      UniProtKB/Swiss-Prot
      Q96A99
      Related
      ENSP00000445277.2, ENST00000447419.7
      Conserved Domains (1) summary
      cd00152
      Location:270467
      PTX; Pentraxins are plasma proteins characterized by their pentameric discoid assembly and their Ca2+ dependent ligand binding, such as Serum amyloid P component (SAP) and C-reactive Protein (CRP), which are cytokine-inducible acute-phase proteins implicated ...

    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_000016.10 Reference GRCh38.p14 Primary Assembly

      Range
      1485886..1488944 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060940.1 Alternate T2T-CHM13v2.0

      Range
      1500922..1503980 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)