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    LINC01790 long intergenic non-protein coding RNA 1790 [ Homo sapiens (human) ]

    Gene ID: 101927431, updated on 10-Dec-2024

    Summary

    Official Symbol
    LINC01790provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 1790provided by HGNC
    Primary source
    HGNC:HGNC:52579
    See related
    Ensembl:ENSG00000230173 AllianceGenome:HGNC:52579
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

    See LINC01790 in Genome Data Viewer
    Location:
    2q32.3
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (194730595..194761435)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (195215864..195246712)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (195595319..195626159)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene Zn regulated GTPase metalloprotein activator 1F pseudogene Neighboring gene small nucleolar RNA SNORD59 Neighboring gene uncharacterized LOC105376755 Neighboring gene NANOG hESC enhancer GRCh37_chr2:195627401-195627902 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:195768635-195768838 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:195937963-195938515 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr2:196077215-196077824 Neighboring gene uncharacterized LOC105373817 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:196278375-196278874 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:196304790-196305290 Neighboring gene RNA, U6 small nuclear 169, pseudogene

    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_110223.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC006196, AK056610
      Related
      ENST00000447194.1

    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_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      194730595..194761435
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      195215864..195246712
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)