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    D21S2088E D21S2088E [ Homo sapiens (human) ]

    Gene ID: 266917, updated on 22-Oct-2024

    Summary

    Gene symbol
    D21S2088E
    Gene description
    D21S2088E
    See related
    Ensembl:ENSG00000228592
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Low expression observed in reference dataset See more
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    Genomic context

    See D21S2088E in Genome Data Viewer
    Location:
    21q21.2
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (23361104..23384835, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (21717188..21740600, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 21 NC_000021.8 (24733426..24757156, complement)

    Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene Myb/SANT DNA binding domain containing 2 pseudogene 1 Neighboring gene RNA, U2 small nuclear 55, pseudogene Neighboring gene eukaryotic translation elongation factor 1 alpha 1 pseudogene 1 Neighboring gene uncharacterized LOC105372747 Neighboring gene tubulin alpha pseudogene 1

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    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_040254.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AP000459, AY063451
      Related
      ENST00000262354.6

    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. NC_000021.9 Reference GRCh38.p14 Primary Assembly

      Range
      23361104..23384835 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060945.1 Alternate T2T-CHM13v2.0

      Range
      21717188..21740600 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)