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RNU6-582P RNA, U6 small nuclear 582, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481365, updated on 17-Sep-2024

Summary

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Official Symbol
RNU6-582Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 582, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47545
See related
Ensembl:ENSG00000199859 AllianceGenome:HGNC:47545
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 RNU6-582P in Genome Data Viewer
Location:
4q32.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (157201563..157201667, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (160547062..160547166, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (158122715..158122819, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:157919659-157920439 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:157920440-157921219 Neighboring gene ribonuclease P RNA component H1, 3 pseudogene Neighboring gene Sharpr-MPRA regulatory region 1911 Neighboring gene glycine receptor beta Neighboring gene chromatin accessibility complex subunit 1 pseudogene Neighboring gene glutamate ionotropic receptor AMPA type subunit 2

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_044596.1 

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

    Range
    157201563..157201667 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    160547062..160547166 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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