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    ELOCP19 elongin C pseudogene 19 [ Homo sapiens (human) ]

    Gene ID: 100462880, updated on 17-Jun-2019

    Summary

    Official Symbol
    ELOCP19provided by HGNC
    Official Full Name
    elongin C pseudogene 19provided by HGNC
    Primary source
    HGNC:HGNC:38155
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    TCEB1P19

    Genomic context

    See ELOCP19 in Genome Data Viewer
    Location:
    1p22.2
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (88829019..88829443)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (89294796..89295099)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene PKN2 antisense RNA 1 Neighboring gene uncharacterized LOC105378838 Neighboring gene Sharpr-MPRA regulatory region 5313 Neighboring gene protein kinase N2 Neighboring gene RNA, U6 small nuclear 125, pseudogene Neighboring gene general transcription factor IIB Neighboring gene shieldin complex subunit 1 pseudogene Neighboring gene kynurenine aminotransferase 3

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    General gene information

    Other Names

    • transcription elongation factor B (SIII), polypeptide 1 pseudogene 19
    • transcription elongation factor B subunit 1 pseudogene 19

    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_022789.2 

      Range
      101..525
      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
      88829019..88829443
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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