U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from GEO Profiles

    • Showing Current items.

    SNORA70C small nucleolar RNA, H/ACA box 70C [ Homo sapiens (human) ]

    Gene ID: 100124538, updated on 28-Oct-2024

    Summary

    Official Symbol
    SNORA70Cprovided by HGNC
    Official Full Name
    small nucleolar RNA, H/ACA box 70Cprovided by HGNC
    Primary source
    HGNC:HGNC:33619
    See related
    Ensembl:ENSG00000207268 AllianceGenome:HGNC:33619
    Gene type
    snoRNA
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    U70C
    Summary
    This gene produces a small nucleolar RNA (snoRNA) that plays a role in post-transcriptional modification. This snoRNA is a type-3 retrotransposed snoRNA, where the ribosomal protein L10 gene on chromosome X is its parental gene, and this, together with part of the parental gene, was subsequently mobilized into an intron of the astrotactin 2 host gene on chromosome 9. This snoRNA contains a H/ACA box, which serves as a guide for the pseudouridylation of selected bases of ribosomal RNA by forming short duplexes with the 18S rRNA U1692, the target for this snoRNA. This gene is specific to human, chimp and orangutan, and is not found in the genomes of rhesus or marmoset. [provided by RefSeq, Jun 2010]
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See SNORA70C in Genome Data Viewer
    Location:
    9q33.1
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (117181066..117181201, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (129374927..129375062, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (119943345..119943480, complement)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene astrotactin 2 Neighboring gene uncharacterized LOC105376238 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr9:119690983-119691925 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:119833416-119834008 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:119834009-119834601 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr9:119857782-119858981 Neighboring gene ReSE screen-validated silencer GRCh37_chr9:119875735-119875911 Neighboring gene uncharacterized LOC105376237 Neighboring gene RN7SK pseudogene 128 Neighboring gene ribosomal protein L10 pseudogene 3

    Genomic regions, transcripts, and products

    General gene information

    Other Names

    • SNORA70C snoRNA
    • U70 type 3 snoRT
    • small nucleolar RNA, H/ACA box 70C (retrotransposed)

    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)

    NEW Try the new Transcript table

    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_003708.4 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AL355608
      Related
      ENST00000384538.1

    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_000009.12 Reference GRCh38.p14 Primary Assembly

      Range
      117181066..117181201 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060933.1 Alternate T2T-CHM13v2.0

      Range
      129374927..129375062 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)