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    LINC02353 long intergenic non-protein coding RNA 2353 [ Homo sapiens (human) ]

    Gene ID: 101927363, updated on 10-Dec-2024

    Summary

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    Official Symbol
    LINC02353provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 2353provided by HGNC
    Primary source
    HGNC:HGNC:53275
    See related
    Ensembl:ENSG00000251329 AllianceGenome:HGNC:53275
    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 LINC02353 in Genome Data Viewer
    Location:
    4p15.1
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (32351038..32353220)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (32325889..32328071)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (32352660..32354842)

    Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2506 Neighboring gene uncharacterized LOC124900845 Neighboring gene uncharacterized LOC102723846 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:32398011-32398729 Neighboring gene uncharacterized LOC107986223 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_78431 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_78443 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:32685598-32686457 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:32749967-32750466 Neighboring gene MPRA-validated peak5018 silencer Neighboring gene uncharacterized LOC124900831

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    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_134672.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC019179, BC043520
      Related
      ENST00000515181.2

    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_000004.12 Reference GRCh38.p14 Primary Assembly

      Range
      32351038..32353220
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060928.1 Alternate T2T-CHM13v2.0

      Range
      32325889..32328071
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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