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    SNORD6 small nucleolar RNA, C/D box 6 [ Homo sapiens (human) ]

    Gene ID: 692075, updated on 13-Feb-2019

    Summary

    Official Symbol
    SNORD6provided by HGNC
    Official Full Name
    small nucleolar RNA, C/D box 6provided by HGNC
    Primary source
    HGNC:HGNC:32703
    See related
    Ensembl:ENSG00000202314
    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
    mgh28S-2412

    Genomic context

    See SNORD6 in Genome Data Viewer
    Location:
    11q21
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    109 current GRCh38.p12 (GCF_000001405.38) 11 NC_000011.10 (93731503..93731573, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (93464669..93464739, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene TATA-box binding protein associated factor, RNA polymerase I subunit D Neighboring gene small nucleolar RNA, H/ACA box 25 Neighboring gene small nucleolar RNA, H/ACA box 32 Neighboring gene small nucleolar RNA, H/ACA box 1 Neighboring gene small nucleolar RNA, H/ACA box 8

    Genomic regions, transcripts, and products

    Bibliography

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Other Names

    • mgh28S-2412 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_003036.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AJ609489
      Related
      ENST00000365444.1

    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.p12 Primary Assembly

    Genomic

    1. NC_000011.10 Reference GRCh38.p12 Primary Assembly

      Range
      93731503..93731573 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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