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    EIF4BP2 eukaryotic translation initiation factor 4B pseudogene 2 [ Homo sapiens (human) ]

    Gene ID: 100129337, updated on 17-Jun-2019

    Summary

    Official Symbol
    EIF4BP2provided by HGNC
    Official Full Name
    eukaryotic translation initiation factor 4B pseudogene 2provided by HGNC
    Primary source
    HGNC:HGNC:37935
    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 EIF4BP2 in Genome Data Viewer
    Location:
    10p12.31
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (21028983..21030793)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (21317928..21319745)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene nebulette Neighboring gene uncharacterized LOC102725112 Neighboring gene Sharpr-MPRA regulatory region 670 Neighboring gene Sharpr-MPRA regulatory region 12489 Neighboring gene nucleophosmin 1 pseudogene 30

    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_022968.3 

      Range
      101..1911
      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_000010.11 Reference GRCh38.p13 Primary Assembly

      Range
      21028983..21030793
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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