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    LINC00536 long intergenic non-protein coding RNA 536 [ Homo sapiens (human) ]

    Gene ID: 100859921, updated on 10-Dec-2024

    Summary

    Official Symbol
    LINC00536provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 536provided by HGNC
    Primary source
    HGNC:HGNC:43645
    See related
    Ensembl:ENSG00000249917 AllianceGenome:HGNC:43645
    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 LINC00536 in Genome Data Viewer
    Location:
    8q23.3
    Exon count:
    14
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (115950511..116325059, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (117077723..117452435, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (116962736..117337297, complement)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986902 Neighboring gene uncharacterized LOC107986903 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:116981560-116982759 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:117041007-117041189 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:117050679-117051374 Neighboring gene RNA, 5S ribosomal pseudogene 276 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:117081592-117081754 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:117101307-117101884 Neighboring gene NANOG hESC enhancer GRCh37_chr8:117108567-117109155 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:117140378-117141004 Neighboring gene NANOG hESC enhancer GRCh37_chr8:117243536-117244062 Neighboring gene Sharpr-MPRA regulatory region 9276 Neighboring gene uncharacterized LOC124902005 Neighboring gene uncharacterized LOC102723447 Neighboring gene uncharacterized LOC105375711

    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

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    A genome-wide association study identifies susceptibility loci for ossification of the posterior longitudinal ligament of the spine.
    EBI GWAS Catalog

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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_046215.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC103863, AF130342, BC040336
      Related
      ENST00000505156.2

    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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      115950511..116325059 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      117077723..117452435 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)