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RNU6-458P RNA, U6 small nuclear 458, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481324, updated on 10-Dec-2024

Summary

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Official Symbol
RNU6-458Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 458, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47421
See related
Ensembl:ENSG00000206906 AllianceGenome:HGNC:47421
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 RNU6-458P in Genome Data Viewer
Location:
14q11.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (18343038..18343144)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (12846337..12846443)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (19119515..19119621)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107987204 Neighboring gene RNA, 18S ribosomal pseudogene Neighboring gene RNA, 5.8S ribosomal pseudogene Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr14:19035899-19036790 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr14:19037816-19038681 Neighboring gene BCL2 interacting protein 3 pseudogene 6 Neighboring gene olfactory receptor family 11 subfamily H member 12

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_044259.1 

    Range
    101..207
    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_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    18343038..18343144
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    12846337..12846443
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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