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    Gm26504 predicted gene, 26504 [ Mus musculus (house mouse) ]

    Gene ID: 64243, updated on 17-Aug-2024

    Summary

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    Official Symbol
    Gm26504provided by MGI
    Official Full Name
    predicted gene, 26504provided by MGI
    Primary source
    MGI:MGI:5456281
    See related
    Ensembl:ENSMUSG00000118899 AllianceGenome:MGI:5456281
    Gene type
    snoRNA
    RefSeq status
    VALIDATED
    Organism
    Mus musculus
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
    Also known as
    Pwcr1; MBII-85; Snord116
    Annotation information
    Annotation category: suggests misassembly
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    Genomic context

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    See Gm26504 in Genome Data Viewer
    Location:
    7 B5; 7
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_02 current GRCm39 (GCF_000001635.27) 7 NC_000073.7 (59325738..59325827, complement)
    108.20200622 previous assembly GRCm38.p6 (GCF_000001635.26) 7 NC_000073.6 (59675990..59676079, complement)

    Chromosome 7 - NC_000073.7Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA host gene 14 Neighboring gene predicted gene, 25870 Neighboring gene predicted gene, 23862 Neighboring gene predicted gene, 22285 Neighboring gene predicted gene, 22131 Neighboring gene imprinted gene in the Prader-Willi syndrome region

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice. Ding F, et al. PLoS One, 2008 Mar 5. PMID 18320030, Free PMC Article
    2. Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models. Ding F, et al. Mamm Genome, 2005 Jun. PMID 16075369
    3. The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene. Watrin F, et al. BMC Genet, 2005 Jan 5. PMID 15634360, Free PMC Article
    4. Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain. Lee S, et al. Gene Expr Patterns, 2003 Oct. PMID 12971993
    5. Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation. Skryabin BV, et al. PLoS Genet, 2007 Dec 28. PMID 18166085, Free PMC Article

    See all (11) citations in PubMed

    GeneRIFs: Gene References Into Functions

    General gene information

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    Markers

    Other Names

    • Prader-Willi chromosome region 1 homolog
    • small nucleolar RNA, C/D box 116 cluster
    • snoRNA MBII-85

    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_002895.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC168073
      Related
      ENSMUST00000102033.4

    RefSeqs of Annotated Genomes: GCF_000001635.27-RS_2024_02

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

    Reference GRCm39 C57BL/6J

    Genomic

    1. NC_000073.7 Reference GRCm39 C57BL/6J

      Range
      59325738..59325827 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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