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    SNORD58C small nucleolar RNA, C/D box 58C [ Homo sapiens (human) ]

    Gene ID: 100124516, updated on 17-Jun-2019

    Summary

    Official Symbol
    SNORD58Cprovided by HGNC
    Official Full Name
    small nucleolar RNA, C/D box 58Cprovided by HGNC
    Primary source
    HGNC:HGNC:33613
    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
    U58

    Genomic context

    See SNORD58C in Genome Data Viewer
    Location:
    18q21.1
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 18 NC_000018.10 (49489235..49489324, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (47015605..47015694, complement)

    Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene chromosome 18 open reading frame 32 Neighboring gene RPL17-C18orf32 readthrough Neighboring gene microRNA 1539 Neighboring gene ribosomal protein L17 Neighboring gene small nucleolar RNA, C/D box 58A Neighboring gene small nucleolar RNA, C/D box 58B

    Genomic regions, transcripts, and products

    Bibliography

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    General gene information

    Other Names

    • SNORD58C snoRNA
    • U58 small nucleolar RNA
    • U58 snoRNA

    Gene Ontology Provided by GOA

    Process Evidence Code Pubs
    RNA processing IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    nucleolus IEA
    Inferred from Electronic Annotation
    more info
     

    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_003701.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC100778

    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_000018.10 Reference GRCh38.p13 Primary Assembly

      Range
      49489235..49489324 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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