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    PRR9 proline rich 9 [ Homo sapiens (human) ]

    Gene ID: 574414, updated on 17-Sep-2024

    Summary

    Official Symbol
    PRR9provided by HGNC
    Official Full Name
    proline rich 9provided by HGNC
    Primary source
    HGNC:HGNC:32057
    See related
    Ensembl:ENSG00000203783 AllianceGenome:HGNC:32057
    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
    Expression
    Low expression observed in reference dataset See more
    Orthologs
    NEW
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    Genomic context

    See PRR9 in Genome Data Viewer
    Location:
    1q21.3
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (153217584..153219310)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (152354127..152355853)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (153190060..153191786)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene small proline rich protein 2G Neighboring gene uncharacterized LOC101928009 Neighboring gene late cornified envelope like proline rich 1 Neighboring gene ribosomal protein lateral stalk subunit P0 pseudogene 4 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1338 Neighboring gene loricrin cornified envelope precursor protein

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues 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

    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_001195571.2NP_001182500.1  proline-rich protein 9

      See identical proteins and their annotated locations for NP_001182500.1

      Status: VALIDATED

      Source sequence(s)
      AI432195, AL161636, BX100130, CD387786
      Consensus CDS
      CCDS55639.1
      UniProtKB/Swiss-Prot
      Q5T870
      Related
      ENSP00000357733.3, ENST00000368744.4
      Conserved Domains (1) summary
      pfam02389
      Location:5116
      Cornifin; Cornifin (SPRR) family

    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_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      153217584..153219310
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      152354127..152355853
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)