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    USP9YP7 USP9Y pseudogene 7 [ Homo sapiens (human) ]

    Gene ID: 100462821, updated on 17-Jun-2024

    Summary

    Official Symbol
    USP9YP7provided by HGNC
    Official Full Name
    USP9Y pseudogene 7provided by HGNC
    Primary source
    HGNC:HGNC:38079
    See related
    AllianceGenome:HGNC:38079
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

    See USP9YP7 in Genome Data Viewer
    Location:
    Yq11.222
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (17910591..17910787)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (18817142..18817338)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (20022471..20022667)

    Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene chromodomain Y-linked 2B Neighboring gene chromodomain Y-linked 6 pseudogene Neighboring gene USP9Y pseudogene 6 Neighboring gene AZFb P5.1 recombination region Neighboring gene chromodomain Y-linked 7 pseudogene

    Genomic regions, transcripts, and products

    NCBI Reference Sequences (RefSeq)

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    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_083997.1 

      Range
      101..297
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      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000024.10 Reference GRCh38.p14 Primary Assembly

      Range
      17910591..17910787
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060948.1 Alternate T2T-CHM13v2.0

      Range
      18817142..18817338
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)