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    SNORD112 small nucleolar RNA, C/D box 112 [ Homo sapiens (human) ]

    Gene ID: 692215, updated on 2-Nov-2024

    Summary

    Official Symbol
    SNORD112provided by HGNC
    Official Full Name
    small nucleolar RNA, C/D box 112provided by HGNC
    Primary source
    HGNC:HGNC:32777
    See related
    Ensembl:ENSG00000275662 MIM:613649; AllianceGenome:HGNC:32777
    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
    14q(0)
    Summary
    Small nucleolar RNAs (snoRNAs), like SNORD112, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]
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    Genomic context

    See SNORD112 in Genome Data Viewer
    Location:
    14q32.2
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (100897920..100897996)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (95133350..95133426)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (101364257..101364333)

    Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 13483 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_33596 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_33604 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:101357417-101357918 Neighboring gene retrotransposon Gag like 1 Neighboring gene microRNA 432 Neighboring gene microRNA 136 Neighboring gene maternally expressed 8, small nucleolar RNA host gene Neighboring gene microRNA 370 Neighboring gene small nucleolar RNA, C/D box 113-1

    Genomic regions, transcripts, and products

    General gene information

    Markers

    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_003080.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL117190
      Related
      ENST00000458974.1

    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_000014.9 Reference GRCh38.p14 Primary Assembly

      Range
      100897920..100897996
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060938.1 Alternate T2T-CHM13v2.0

      Range
      95133350..95133426
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)