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RNU6-457P RNA, U6 small nuclear 457, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479768, updated on 21-Mar-2023

Summary

Official Symbol
RNU6-457Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 457, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47420
See related
Ensembl:ENSG00000200869 AllianceGenome:HGNC:47420
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

See RNU6-457P in Genome Data Viewer
Location:
16p13.3
Annotation release Status Assembly Chr Location
RS_2023_03 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (6873899..6874005)
RS_2023_03 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (6904067..6904173)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (6923900..6924006)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene RNA binding fox-1 homolog 1 Neighboring gene meiotic recombination hotspot CG Neighboring gene RNA, U7 small nuclear 99 pseudogene Neighboring gene uncharacterized LOC105371068 Neighboring gene RNA, U6 small nuclear 328, pseudogene

Genomic regions, transcripts, and products

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_045708.1 

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

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_03

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    6873899..6874005
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    6904067..6904173
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)