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    LURAP1L-AS1 LURAP1L antisense RNA 1 [ Homo sapiens (human) ]

    Gene ID: 101929467, updated on 17-Jun-2024

    Summary

    Official Symbol
    LURAP1L-AS1provided by HGNC
    Official Full Name
    LURAP1L antisense RNA 1provided by HGNC
    Primary source
    HGNC:HGNC:49761
    See related
    Ensembl:ENSG00000235448 AllianceGenome:HGNC:49761
    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

    See LURAP1L-AS1 in Genome Data Viewer
    Location:
    9p23
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (12699999..12814389, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (12709327..12823714, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (12699999..12814388, complement)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:12334327-12334960 Neighboring gene JNK1/MAPK8-associated membrane protein pseudogene 1 Neighboring gene RNA, U2 small nuclear 47, pseudogene Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:12438630-12439130 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:12439131-12439631 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:12440846-12441628 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:12463247-12463746 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 9:12581404 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 9:12636264 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 9:12651340 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 9:12660541 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 9:12671566 Neighboring gene melanoma risk locus-associated MPRA allelic enhancers 9:12675264 and 9:12675284 Neighboring gene tyrosinase related protein 1 Neighboring gene RNA, 7SL, cytoplasmic 849, pseudogene Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:12814001-12815200 Neighboring gene leucine rich adaptor protein 1 like Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr9:12948228-12949066 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr9:12953525-12954183 Neighboring gene small nucleolar RNA, C/D box 137 Neighboring gene lupus La protein-like Neighboring gene peroxiredoxin 1 pseudogene 1 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:13037568-13038084

    Genomic regions, transcripts, and products

    Expression

    • 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

    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_125775.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AI521216, BQ416907, DA711357
      Related
      ENST00000417638.1

    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_000009.12 Reference GRCh38.p14 Primary Assembly

      Range
      12699999..12814389 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060933.1 Alternate T2T-CHM13v2.0

      Range
      12709327..12823714 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)