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    LINC01757 long intergenic non-protein coding RNA 1757 [ Homo sapiens (human) ]

    Gene ID: 105376827, updated on 22-Oct-2024

    Summary

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    Official Symbol
    LINC01757provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 1757provided by HGNC
    Primary source
    HGNC:HGNC:52546
    See related
    Ensembl:ENSG00000228105 AllianceGenome:HGNC:52546
    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 LINC01757 in Genome Data Viewer
    Location:
    1p36.12
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (20243095..20244655)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (20066752..20068312)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (20569588..20571148)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376825 Neighboring gene uncharacterized LOC105376826 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:20537509-20538708 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 363 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 318 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 319 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr1:20592229-20593428 Neighboring gene uncharacterized LOC105376828 Neighboring gene NANOG hESC enhancer GRCh37_chr1:20605144-20605685 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:20616749-20617260 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:20617261-20617771 Neighboring gene von Willebrand factor A domain containing 5B1 Neighboring gene uncharacterized LOC124903870

    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 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)

    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_147205.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      BX094500, Z98257
      Related
      ENST00000435552.2

    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_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      20243095..20244655
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      20066752..20068312
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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