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    STAU2P1 STAU2 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 100130134, updated on 17-Sep-2024

    Summary

    Official Symbol
    STAU2P1provided by HGNC
    Official Full Name
    STAU2 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:55011
    See related
    AllianceGenome:HGNC:55011
    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 STAU2P1 in Genome Data Viewer
    Location:
    Xq21.31
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (90037863..90040928, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (88478960..88482025, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (89292862..89295927, complement)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC102724150 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:88660958-88661203 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:88687522-88688285 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:88961378-88962128 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:88962129-88962877 Neighboring gene TGFB induced factor homeobox 2 like X-linked Neighboring gene USP12 pseudogene X-linked Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:89433889-89434419 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:89443856-89444691 Neighboring gene ring finger protein 19B pseudogene X-linked

    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_022618.3 

      Range
      101..3166
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      90037863..90040928 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      88478960..88482025 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)