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    APOOP2 apolipoprotein O pseudogene 2 [ Homo sapiens (human) ]

    Gene ID: 100129005, updated on 15-Jun-2019

    Summary

    Official Symbol
    APOOP2provided by HGNC
    Official Full Name
    apolipoprotein O pseudogene 2provided by HGNC
    Primary source
    HGNC:HGNC:48740
    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 APOOP2 in Genome Data Viewer
    Location:
    3p11.2
    Annotation release Status Assembly Chr Location
    109 current GRCh38.p12 (GCF_000001405.38) 3 NC_000003.12 (87594806..87595384)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (87643956..87644534)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene POU class 1 homeobox 1 Neighboring gene keratin 8 pseudogene 25 Neighboring gene proteasome 26S subunit, ATPase 1 pseudogene 6 Neighboring gene uncharacterized LOC105377198

    Genomic regions, transcripts, and products

    Bibliography

    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_012899.1 

      Range
      101..679
      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_000003.12 Reference GRCh38.p13 Primary Assembly

      Range
      87594806..87595384
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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