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    RNU6-464P RNA, U6 small nuclear 464, pseudogene [ Homo sapiens (human) ]

    Gene ID: 106479771, updated on 17-Sep-2024

    Summary

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    Official Symbol
    RNU6-464Pprovided by HGNC
    Official Full Name
    RNA, U6 small nuclear 464, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:47427
    See related
    Ensembl:ENSG00000253026 AllianceGenome:HGNC:47427
    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 RNU6-464P in Genome Data Viewer
    Location:
    6p12.1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (53153795..53153898, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (52993404..52993507, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (53018593..53018696, complement)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene F-box protein 9 Neighboring gene RNA, 7SL, cytoplasmic 244, pseudogene Neighboring gene Sharpr-MPRA regulatory region 2296 Neighboring gene glial cells missing transcription factor 1 Neighboring gene uncharacterized LOC124901513 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_92170 Neighboring gene superoxide dismutase 1 pseudogene 1 Neighboring gene RNA, U1 small nuclear 136, pseudogene

    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_044129.1 

      Range
      101..204
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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_000006.12 Reference GRCh38.p14 Primary Assembly

      Range
      53153795..53153898 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060930.1 Alternate T2T-CHM13v2.0

      Range
      52993404..52993507 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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