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    LINC00302 long intergenic non-protein coding RNA 302 [ Homo sapiens (human) ]

    Gene ID: 388699, updated on 10-Dec-2024

    Summary

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    Official Symbol
    LINC00302provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 302provided by HGNC
    Primary source
    HGNC:HGNC:31825
    See related
    Ensembl:ENSG00000304384 AllianceGenome:HGNC:31825
    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
    xp33; C1orf46; NCRNA00302
    Expression
    Restricted expression toward skin (RPKM 21.0) See more
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    Genomic context

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    See LINC00302 in Genome Data Viewer
    Location:
    1q21.3
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (152655477..152656804)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (151792023..151793350)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (152627953..152629280)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene late cornified envelope 3A Neighboring gene late cornified envelope pseudogene 4 Neighboring gene late cornified envelope pseudogene 3 Neighboring gene late cornified envelope 2D Neighboring gene late cornified envelope 2C

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. Landscape of Long Noncoding RNAs in Psoriatic and Healthy Skin. Gupta R, et al. J Invest Dermatol, 2016 Mar. PMID 27015450, Free PMC Article
    2. Positional cloning of novel skin-specific genes from the human epidermal differentiation complex. Zhao XP, et al. Genomics, 1997 Oct 15. PMID 9344646

    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_145430.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL139247
      Related
      ENST00000803094.1

    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_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      152655477..152656804
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      151792023..151793350
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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