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    SCARNA22 small Cajal body-specific RNA 22 [ Homo sapiens (human) ]

    Gene ID: 677770, updated on 7-Jun-2015
    Official Symbol
    SCARNA22provided by HGNC
    Official Full Name
    small Cajal body-specific RNA 22provided by HGNC
    Primary source
    HGNC:HGNC:32580
    Gene type
    ncRNA
    RefSeq status
    PROVISIONAL
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ACA11
    See SCARNA22 in Epigenomics, MapViewer
    Location:
    4p16.3
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    107 current GRCh38.p2 (GCF_000001405.28) 4 NC_000004.12 (1974636..1974760)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (1976363..1976487)

    Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene fibroblast growth factor receptor 3 Neighboring gene leucine zipper-EF-hand containing transmembrane protein 1 Neighboring gene Wolf-Hirschhorn syndrome candidate 1 Neighboring gene negative elongation factor complex member A Neighboring gene microRNA 943 Neighboring gene chromosome 4 open reading frame 48

    Products Interactant Other Gene Complex Source Pubs Description

    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_003004.1 RNA Sequence

      Status: PROVISIONAL

      Source sequence(s)
      AJ609470

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 107

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

    Reference GRCh38.p2 Primary Assembly

    Genomic

    1. NC_000004.12 Reference GRCh38.p2 Primary Assembly

      Range
      1974636..1974760
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate CHM1_1.1

    Genomic

    1. NC_018915.2 Alternate CHM1_1.1

      Range
      1975026..1975150
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)