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    LINC01549 long intergenic non-protein coding RNA 1549 [ Homo sapiens (human) ]

    Gene ID: 100505929, updated on 10-Dec-2024

    Summary

    Official Symbol
    LINC01549provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 1549provided by HGNC
    Primary source
    HGNC:HGNC:1277
    See related
    Ensembl:ENSG00000232560 AllianceGenome:HGNC:1277
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    C21orf37
    Expression
    Low expression observed in reference dataset See more
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    Genomic context

    See LINC01549 in Genome Data Viewer
    Location:
    21q21.1
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (17438890..17449185)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (15793985..15804295)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 21 NC_000021.8 (18811208..18821503)

    Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985511 Neighboring gene NIMA-related kinase 4 pseudogene 1 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr21:18652025-18652526 Neighboring gene MPRA-validated peak4348 silencer Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr21:18743116-18744315 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr21:18790767-18791966 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr21:18810837-18811420 Neighboring gene RNA, U6 small nuclear 113, pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 18293 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13220 Neighboring gene tRNA-Gly (anticodon GCC) 1-5 Neighboring gene Sharpr-MPRA regulatory region 2602 Neighboring gene ribosomal protein L39 pseudogene 40

    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

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    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_037585.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longer transcript.
      Source sequence(s)
      AI420675, AP000952, BC130500, BX089409
      Related
      ENST00000736550.1
    2. NR_037586.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) uses an alternate splice site resulting in a shorter transcript, compared to variant 1.
      Source sequence(s)
      AI420675, AP000952, BC144391, BX089409

    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_000021.9 Reference GRCh38.p14 Primary Assembly

      Range
      17438890..17449185
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060945.1 Alternate T2T-CHM13v2.0

      Range
      15793985..15804295
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001005521.1: Suppressed sequence

      Description
      NM_001005521.1: This RefSeq was permanently suppressed because it was mostly repetitive sequence.