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    RNU6-34P RNA, U6 small nuclear 34, pseudogene [ Homo sapiens (human) ]

    Gene ID: 100873749, updated on 17-Sep-2024

    Summary

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    Official Symbol
    RNU6-34Pprovided by HGNC
    Official Full Name
    RNA, U6 small nuclear 34, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:34278
    See related
    Ensembl:ENSG00000201744 AllianceGenome:HGNC:34278
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    RNU6-34
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    Genomic context

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    See RNU6-34P in Genome Data Viewer
    Location:
    4q22.3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (96152299..96152403, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (99467312..99467416, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (97073450..97073554, complement)

    Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:96760761-96761262 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:96761263-96761762 Neighboring gene NANOG hESC enhancer GRCh37_chr4:96791095-96791601 Neighboring gene RNA, U6 small nuclear 1059, pseudogene Neighboring gene pyruvate dehydrogenase E1 subunit alpha 2 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:96862743-96863244 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:96863245-96863744 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:97023059-97024258 Neighboring gene talin 2 pseudogene Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:97148613-97149159 Neighboring gene NANOG hESC enhancer GRCh37_chr4:97173200-97173733 Neighboring gene NANOG hESC enhancer GRCh37_chr4:97181156-97181836 Neighboring gene long intergenic non-protein coding RNA 2267 Neighboring gene RN7SK pseudogene 28

    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)

    See Variation Viewer (GRCh38)

    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_043073.1 

      Range
      101..205
      Download
      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_000004.12 Reference GRCh38.p14 Primary Assembly

      Range
      96152299..96152403 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060928.1 Alternate T2T-CHM13v2.0

      Range
      99467312..99467416 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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