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    LINC02819 long intergenic non-protein coding RNA 2819 [ Homo sapiens (human) ]

    Gene ID: 105371462, updated on 10-Oct-2023

    Summary

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    Official Symbol
    LINC02819provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 2819provided by HGNC
    Primary source
    HGNC:HGNC:54350
    See related
    AllianceGenome:HGNC:54350
    Gene type
    ncRNA
    RefSeq status
    MODEL
    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 LINC02819 in Genome Data Viewer
    Location:
    1q23.2
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (159466095..159490029)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (158603227..158627156)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene olfactory receptor family 10 subfamily J member 1 Neighboring gene olfactory receptor family 10 subfamily J member 9 pseudogene Neighboring gene Sharpr-MPRA regulatory region 7346 Neighboring gene olfactory receptor family 10 subfamily J member 4 (gene/pseudogene) Neighboring gene olfactory receptor family 10 subfamily J member 5 Neighboring gene amyloid P component, serum pseudogene

    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

    Genotypes

    NCBI Reference Sequences (RefSeq)

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    NEW Try the new Transcript table

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

    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
      159466095..159490029
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_922189.4 RNA Sequence

    2. XR_922190.3 RNA Sequence

    Reference GRCh38.p14 PATCHES

    Genomic

    1. NW_025791759.1 Reference GRCh38.p14 PATCHES

      Range
      217922..241856
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007069449.1 RNA Sequence

    2. XR_007069450.1 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      158603227..158627156
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007070769.1 RNA Sequence

    2. XR_007070770.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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