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    LOC101927531 uncharacterized LOC101927531 [ Homo sapiens (human) ]

    Gene ID: 101927531, updated on 10-Dec-2024

    Summary

    Gene symbol
    LOC101927531
    Gene description
    uncharacterized LOC101927531
    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 LOC101927531 in Genome Data Viewer
    Location:
    12q24.32
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (126358019..126361065)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (126366780..126369826)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (126842565..126845611)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene transmembrane protein 132C pseudogene Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr12:126717441-126718421 Neighboring gene NANOG hESC enhancer GRCh37_chr12:126727348-126727849 Neighboring gene uncharacterized LOC105379613 Neighboring gene ReSE screen-validated silencer GRCh37_chr12:126835877-126836032 Neighboring gene uncharacterized LOC107984448 Neighboring gene uncharacterized LOC124903048 Neighboring gene long intergenic non-protein coding RNA 2825

    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_187677.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC007368

    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_000012.12 Reference GRCh38.p14 Primary Assembly

      Range
      126358019..126361065
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NW_003315940.1 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      136864..139910
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060936.1 Alternate T2T-CHM13v2.0

      Range
      126366780..126369826
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)