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    RNU6-1151P RNA, U6 small nuclear 1151, pseudogene [ Homo sapiens (human) ]

    Gene ID: 106481543, updated on 10-Oct-2023

    Summary

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    Official Symbol
    RNU6-1151Pprovided by HGNC
    Official Full Name
    RNA, U6 small nuclear 1151, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:48114
    See related
    Ensembl:ENSG00000207415 AllianceGenome:HGNC:48114
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

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    Location:
    8p23.1
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (9287472..9287578, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (10456402..10456509)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (9144982..9145088, complement)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:9046079-9047278 Neighboring gene uncharacterized LOC101929128 Neighboring gene ubiquitin-conjugating enzyme E2 variant 1-like Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:9106826-9107326 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:9114015-9114515 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr8:9120655-9121382 Neighboring gene Sharpr-MPRA regulatory region 719 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:9127271-9127799 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:9134231-9134732 Neighboring gene uncharacterized LOC124901883 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:9176485-9176986 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:9176987-9177486 Neighboring gene uncharacterized LOC157273

    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 studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    General gene information

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    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.

    Genomic

    1. NG_043973.1 

      Range
      101..207
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      9287472..9287578 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      10456402..10456509
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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