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RNU6-526P RNA, U6 small nuclear 526, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481347, updated on 8-Nov-2023

Summary

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Official Symbol
RNU6-526Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 526, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47489
See related
Ensembl:ENSG00000201815 AllianceGenome:HGNC:47489
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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Location:
8p23.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (9371090..9371195, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (10372737..10372842)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (9228600..9228705, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC157273 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:9195231-9196164 Neighboring gene uncharacterized LOC105379228 Neighboring gene uncharacterized LOC105379231 Neighboring gene Sharpr-MPRA regulatory region 4717 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:9222619-9223123 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26982 Neighboring gene uncharacterized LOC105379230 Neighboring gene uncharacterized LOC124901884 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr8:9240606-9241805

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_044454.1 

    Range
    101..206
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    9371090..9371195 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_018654717.1 Reference GRCh38.p14 PATCHES

    Range
    3980336..3980441
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    10372737..10372842
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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