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    RPS6P17 ribosomal protein S6 pseudogene 17 [ Homo sapiens (human) ]

    Gene ID: 120318, updated on 19-May-2026
    Official Symbol
    RPS6P17provided by HGNC
    Official Full Name
    ribosomal protein S6 pseudogene 17provided by HGNC
    Primary source
    HGNC:HGNC:36669
    See related
    Ensembl:ENSG00000243777 AllianceGenome:HGNC:36669
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    RPS6_7_1168
    Try the new Gene page
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    See RPS6P17 in Genome Data Viewer
    Location:
    11q22.1
    Annotation release Status Assembly Chr Location
    RS_2025_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (102295019..102295839)
    RS_2025_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (102297137..102297957)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (102165750..102166570)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene YAP1 divergent transcript Neighboring gene Yes1 associated transcriptional regulator Neighboring gene Sharpr-MPRA regulatory region 8516 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:102131708-102132212 Neighboring gene uncharacterized LOC105369460 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3860 Neighboring gene Sharpr-MPRA regulatory region 9487 Neighboring gene uncharacterized LOC124902739 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr11:102187662-102188861 Neighboring gene RNA, U6 small nuclear 952, pseudogene

    Go to nucleotide: Graphics FASTA GenBank

    Related articles in PubMed

    1. Comparative analysis of processed ribosomal protein pseudogenes in four mammalian genomes. Balasubramanian S, et al. Genome Biol, 2009. PMID 19123937, Free PMC Article

    GeneRIFs: Gene References Into Functions

    Review eQTL and phenotype association data in this region using PheGenI

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    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_011320.1 

      Range
      101..921
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2025_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      102295019..102295839
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      102297137..102297957
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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