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    RN7SKP189 RN7SK pseudogene 189 [ Homo sapiens (human) ]

    Gene ID: 106479180, updated on 17-Sep-2024

    Summary

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    Official Symbol
    RN7SKP189provided by HGNC
    Official Full Name
    RN7SK pseudogene 189provided by HGNC
    Primary source
    HGNC:HGNC:45913
    See related
    AllianceGenome:HGNC:45913
    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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    See RN7SKP189 in Genome Data Viewer
    Location:
    Xq27.3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (145057108..145057347)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (143316010..143316249)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (144138628..144138867)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ribonucleotide reductase M2 polypeptide pseudogene 4 Neighboring gene NANOG hESC enhancer GRCh37_chrX:143834881-143835457 Neighboring gene NANOG hESC enhancer GRCh37_chrX:143855361-143855862 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:143882879-143884078 Neighboring gene heterogeneous nuclear ribonucleoprotein C pseudogene 10 Neighboring gene CYCS pseudogene 44 Neighboring gene SPANX family member N1

    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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    Other Names

    • RNA, 7SK small nuclear pseudogene 189

    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_043528.1 

      Range
      101..340
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      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      145057108..145057347
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      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      143316010..143316249
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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