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    MGC70870 C-terminal binding protein 2 pseudogene [ Homo sapiens (human) ]

    Gene ID: 403340, updated on 10-Dec-2024

    Summary

    Gene symbol
    MGC70870
    Gene description
    C-terminal binding protein 2 pseudogene
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    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 MGC70870 in Genome Data Viewer
    Location:
    chromosome: 17
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 Unlocalized Scaffold NT_113930.2 (54857..57966, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 Unlocalized Scaffold NT_113930.1 (116623..119732)

    NT_113930.2Genomic Context describing neighboring genes Neighboring gene VCP nuclear cofactor family member 2 pseudogene Neighboring gene carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2-like Neighboring gene uncharacterized LOC105379281

    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.

    RNA

    1. NR_003682.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC011841, AK092162, BC106037, DA695335

    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. NT_113930.2 Reference GRCh38.p14 Primary Assembly

      Range
      54857..57966 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)