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    PRR27 proline rich 27 [ Homo sapiens (human) ]

    Gene ID: 401137, updated on 5-Mar-2024

    Summary

    Official Symbol
    PRR27provided by HGNC
    Official Full Name
    proline rich 27provided by HGNC
    Primary source
    HGNC:HGNC:33193
    See related
    Ensembl:ENSG00000187533 AllianceGenome:HGNC:33193
    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
    C4orf40
    Summary
    Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]
    Expression
    Restricted expression toward salivary gland (RPKM 399.7) See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See PRR27 in Genome Data Viewer
    Location:
    4q13.3
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (70154237..70166609)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (73493513..73505908)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (71019954..71032326)

    Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene casein alpha s2 like A, pseudogene Neighboring gene casein alpha s2 like B, pseudogene Neighboring gene uncharacterized LOC105377270 Neighboring gene odontogenic, ameloblast associated

    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

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    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_214711.4NP_999876.2  proline-rich protein 27 precursor

      See identical proteins and their annotated locations for NP_999876.2

      Status: VALIDATED

      Source sequence(s)
      AC104811, BX485867, BX640892, BX647183, BX647185, BX648872, BX648896
      Consensus CDS
      CCDS3535.1
      UniProtKB/Swiss-Prot
      A8MXP0, Q6MZM9, Q6MZR6
      Related
      ENSP00000343172.5, ENST00000344526.10

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

      Range
      70154237..70166609
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 PATCHES

    Genomic

    1. NW_013171801.1 Reference GRCh38.p14 PATCHES

      Range
      198823..211195
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060928.1 Alternate T2T-CHM13v2.0

      Range
      73493513..73505908
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)