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    LINC02368 long intergenic non-protein coding RNA 2368 [ Homo sapiens (human) ]

    Gene ID: 101927694, updated on 10-Dec-2024

    Summary

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    Official Symbol
    LINC02368provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 2368provided by HGNC
    Primary source
    HGNC:HGNC:53291
    See related
    Ensembl:ENSG00000256659 AllianceGenome:HGNC:53291
    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

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    See LINC02368 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 (128118217..128121952)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (128148552..128152287)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (128602762..128606497)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370071 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:128594461-128594961 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:128596315-128597514 Neighboring gene long intergenic non-protein coding RNA 2369 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:128642903-128643556 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:128674654-128675653 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:128743759-128744260 Neighboring gene uncharacterized LOC107987176 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:128750861-128751382 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:128751918-128752756 Neighboring gene transmembrane protein 132C Neighboring gene microRNA 3612

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    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_104648.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AK125770
      Related
      ENST00000541258.2

    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
      128118217..128121952
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060936.1 Alternate T2T-CHM13v2.0

      Range
      128148552..128152287
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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