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    LOC101927450 uncharacterized LOC101927450 [ Homo sapiens (human) ]

    Gene ID: 101927450, updated on 10-Dec-2024

    Summary

    Gene symbol
    LOC101927450
    Gene description
    uncharacterized LOC101927450
    See related
    Ensembl:ENSG00000260995
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Low expression observed in reference dataset See more
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    Genomic context

    See LOC101927450 in Genome Data Viewer
    Location:
    9q21.31
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (79135422..79145666, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (91293844..91304088, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (81750337..81760581, complement)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376097 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:81486161-81487360 Neighboring gene Sharpr-MPRA regulatory region 1407 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:81637359-81638558 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr9:81640860-81642059 Neighboring gene keratin 18 pseudogene 24 Neighboring gene uncharacterized LOC124902186 Neighboring gene VISTA enhancer hs765 Neighboring gene VISTA enhancer hs313 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:81975510-81976401 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:81976953-81977508 Neighboring gene coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 9

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    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_109771.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL512634, BC042427
      Related
      ENST00000566873.1

    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
      79135422..79145666 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060933.1 Alternate T2T-CHM13v2.0

      Range
      91293844..91304088 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)