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    SNORD59A small nucleolar RNA, C/D box 59A [ Homo sapiens (human) ]

    Gene ID: 26789, updated on 21-Dec-2019

    Summary

    Official Symbol
    SNORD59Aprovided by HGNC
    Official Full Name
    small nucleolar RNA, C/D box 59Aprovided by HGNC
    Primary source
    HGNC:HGNC:10210
    See related
    Ensembl:ENSG00000207031
    Gene type
    snoRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    U59; RNU59

    Genomic context

    See SNORD59A in Genome Data Viewer
    Location:
    12q13.3
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    109.20191205 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (56645027..56645101, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (57038811..57038885, complement)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 9353 Neighboring gene ATP synthase F1 subunit beta Neighboring gene small nucleolar RNA, C/D box 59B Neighboring gene prostaglandin E synthase 3 Neighboring gene RNA, 7SL, cytoplasmic 809, pseudogene Neighboring gene nascent polypeptide associated complex subunit alpha

    Genomic regions, transcripts, and products

    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.

    RNA

    1. NR_002737.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      X96659
      Related
      ENST00000384304.1

    RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20191205

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000012.12 Reference GRCh38.p13 Primary Assembly

      Range
      56645027..56645101 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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