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    DGCR5 DiGeorge syndrome critical region gene 5 (non-protein coding) [ Homo sapiens (human) ]

    Gene ID: 26220, updated on 26-Feb-2013
    Official Symbol
    DGCR5provided by HGNC
    Official Full Name
    DiGeorge syndrome critical region gene 5 (non-protein coding)provided by HGNC
    Primary source
    HGNC:16757
    Gene type
    miscRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    LINC00037; NCRNA00037
    Location :
    22q11
    Sequence :
    Chromosome: 22; NC_000022.10 (18958011..18982142)
    See DGCR5 in Epigenomics, MapViewer

    Chromosome 22 - NC_000022.10Genomic Context describing neighboring genes Neighboring gene DiGeorge syndrome critical region gene 6 Neighboring gene proline dehydrogenase (oxidase) 1 Neighboring gene cadherin EGF LAG seven-pass G-type receptor 1-like Neighboring gene uncharacterized LOC100287576 Neighboring gene uncharacterized LOC100506454 Neighboring gene DiGeorge syndrome critical region gene 9

    Related articles in PubMed

    GeneRIFs: Gene References Into Functions What's a GeneRIF?

    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_002733.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) is the longer transcript.
      Source sequence(s)
      AC007326, AI566862, BF313645, BG699848
    2. NR_045121.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) lacks an internal exon, compared to variant 1.
      Source sequence(s)
      AC007326, AI566862, BF313645, BG699848

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 104

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh37.p10 Primary Assembly

    Genomic

    1. NC_000022.10 Reference GRCh37.p10 Primary Assembly

      Range
      18958011..18982142
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate HuRef

    Genomic

    1. AC_000154.1 Alternate HuRef

      Range
      2579231..2603251
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate CHM1_1.0

    Genomic

    1. NC_018933.1 Alternate CHM1_1.0

      Range
      2901418..2925518
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

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