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    SNORD70 small nucleolar RNA, C/D box 70 [ Homo sapiens (human) ]

    Gene ID: 692110, updated on 2-Nov-2024

    Summary

    Official Symbol
    SNORD70provided by HGNC
    Official Full Name
    small nucleolar RNA, C/D box 70provided by HGNC
    Primary source
    HGNC:HGNC:32731
    See related
    Ensembl:ENSG00000212534 AllianceGenome:HGNC:32731
    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
    HBII-234; SNORD70A
    Summary
    Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Nov 2024]
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    Genomic context

    See SNORD70 in Genome Data Viewer
    Location:
    2q33.1
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (202276431..202276518)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (202757466..202757553)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (203141154..203141241)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene small ubiquitin like modifier 1 Neighboring gene ribosomal protein L39 pseudogene 14 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12240 Neighboring gene short transmembrane mitochondrial protein 1 pseudogene Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:203114251-203114982 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:203114983-203115714 Neighboring gene NOP58 ribonucleoprotein Neighboring gene small nucleolar RNA, C/D box 70B Neighboring gene small nucleolar RNA, C/D box 11B

    Genomic regions, transcripts, and products

    General gene information

    Gene Ontology Provided by GOA

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

    NCBI Reference Sequences (RefSeq)

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    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_003058.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC064836
      Related
      ENST00000391232.1

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      202276431..202276518
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      202757466..202757553
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)