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    LINC01115 long intergenic non-protein coding RNA 1115 [ Homo sapiens (human) ]

    Gene ID: 339822, updated on 17-Jun-2024

    Summary

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    Official Symbol
    LINC01115provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 1115provided by HGNC
    Primary source
    HGNC:HGNC:49258
    See related
    Ensembl:ENSG00000237667 AllianceGenome:HGNC:49258
    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 LINC01115 in Genome Data Viewer
    Location:
    2p25.3
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (779840..868426, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (779055..867892, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (779837..864112, complement)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105373358 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 15218 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:720518-721018 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:725085-725586 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:726648-727445 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:727446-728242 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:729041-729836 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:729837-730634 Neighboring gene uncharacterized LOC105373480 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:766549-767048 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:776200-776860 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:816439-816939 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr2:826030-826932 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr2:826933-827834 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr2:850078-851277 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr2:863929-865128 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:875979-876480 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 15219 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:886383-886882 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:905231-905732 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:906278-906778 Neighboring gene long intergenic non-protein coding RNA 1939 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:932826-933706 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11102 Neighboring gene SNTG2 antisense RNA 1 Neighboring gene syntrophin gamma 2

    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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    Related articles in PubMed

    1. Chromatin profiling of cortical neurons identifies individual epigenetic signatures in schizophrenia. Gusev FE, et al. Transl Psychiatry, 2019 Oct 17. PMID 31624234, Free PMC Article
    2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, Free PMC Article

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Chromatin profiling of cortical neurons identifies individual epigenetic signatures in schizophrenia.
      Title: Chromatin profiling of cortical neurons identifies individual epigenetic signatures in schizophrenia.
    Submit: New GeneRIF Correction

    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)

    See Variation Viewer (GRCh38)

    Genotypes

    General gene information

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    Markers

    Clone Names

    • AC113607.1

    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_033880.3 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longer transcript.
      Source sequence(s)
      AC113607, AC116609, BC043553
      Related
      ENST00000621134.4

    2. NR_111963.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) lacks an alternate internal exon, resulting in a shorter transcript, compared to variant 1.
      Source sequence(s)
      AC113607, AC116609, BC043553, BC128532

    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_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      779840..868426 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NT_187525.1 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      55780..130160 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      779055..867892 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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