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    HMGB1P26 high mobility group box 1 pseudogene 26 [ Homo sapiens (human) ]

    Gene ID: 645201, updated on 15-Jun-2019

    Summary

    Official Symbol
    HMGB1P26provided by HGNC
    Official Full Name
    high mobility group box 1 pseudogene 26provided by HGNC
    Primary source
    HGNC:HGNC:39117
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Genomic context

    See HMGB1P26 in Genome Data Viewer
    Location:
    1q42.13
    Annotation release Status Assembly Chr Location
    109 current GRCh38.p12 (GCF_000001405.38) 1 NC_000001.11 (229705011..229706022, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (229840958..229841610, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene URB2 ribosome biogenesis homolog Neighboring gene KIAA1191 pseudogene Neighboring gene uncharacterized LOC105373161 Neighboring gene uncharacterized LOC107985464

    Genomic regions, transcripts, and products

    Bibliography

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    NCBI Reference Sequences (RefSeq)

    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_022758.2 

      Range
      42..1053
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

      Range
      229705011..229706022 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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