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    LINC00445 long intergenic non-protein coding RNA 445 [ Homo sapiens (human) ]

    Gene ID: 100507114, updated on 10-Dec-2024

    Summary

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    Official Symbol
    LINC00445provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 445provided by HGNC
    Primary source
    HGNC:HGNC:42782
    See related
    Ensembl:ENSG00000236036 AllianceGenome:HGNC:42782
    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
    Restricted expression toward testis (RPKM 1.7) See more
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    Genomic context

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    See LINC00445 in Genome Data Viewer
    Location:
    13q13.3
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (35697524..35699256)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (34915799..34917504)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (36271661..36273393)

    Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370161 Neighboring gene uncharacterized LOC124903224 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:36270618-36271214 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:36271215-36271810 Neighboring gene NANOG hESC enhancer GRCh37_chr13:36286938-36287653 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:36294554-36295054 Neighboring gene NANOG hESC enhancer GRCh37_chr13:36363862-36364363 Neighboring gene doublecortin like kinase 1 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr13:36429462-36430661 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:36431613-36432152 Neighboring gene uncharacterized LOC105370163 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:36432695-36433234 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr13:36466409-36467608 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:36490885-36491627 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:36496595-36497587 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7587 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7588 Neighboring gene NANOG hESC enhancer GRCh37_chr13:36567619-36568120 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr13:36587826-36589025 Neighboring gene nuclear-encoded mitochondrial tRNA-Gln (TTG) 10-1

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    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

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    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_132115.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longer transcript.
      Source sequence(s)
      AL139083

    2. NR_132116.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) differs in the 5' exon and contains a shorter 3' exon, resulting in a shorter transcript than variant 1.
      Source sequence(s)
      AL139083
      Related
      ENST00000422430.1

    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_000013.11 Reference GRCh38.p14 Primary Assembly

      Range
      35697524..35699256
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060937.1 Alternate T2T-CHM13v2.0

      Range
      34915799..34917504
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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