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    RNU6-46P RNA, U6 small nuclear 46, pseudogene [ Homo sapiens (human) ]

    Gene ID: 100873760, updated on 17-Sep-2024

    Summary

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    Official Symbol
    RNU6-46Pprovided by HGNC
    Official Full Name
    RNA, U6 small nuclear 46, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:34290
    See related
    Ensembl:ENSG00000206587 AllianceGenome:HGNC:34290
    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
    RNU6-46
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    Genomic context

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    See RNU6-46P in Genome Data Viewer
    Location:
    11q13.2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (67895631..67895736)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (67899251..67899356)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (67663102..67663207)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene translation initiation factor IF-2-like Neighboring gene ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 7 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67593458-67593966 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67593967-67594475 Neighboring gene NANOG hESC enhancer GRCh37_chr11:67610458-67611043 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr11:67624072-67624744 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67640251-67640752 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67640753-67641252 Neighboring gene long intergenic non-protein coding RNA 2754 Neighboring gene small nuclear ribonucleoprotein polypeptide C pseudogene 12 Neighboring gene RPS3A pseudogene 40

    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_043165.2 

      Range
      101..206
      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_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      67895631..67895736
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      67899251..67899356
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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