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RNU6-211P RNA, U6 small nuclear 211, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479660, updated on 4-Mar-2025

Summary

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Official Symbol
RNU6-211Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 211, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47174
See related
Ensembl:ENSG00000206774 AllianceGenome:HGNC:47174
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 RNU6-211P in Genome Data Viewer
Location:
5q14.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (80365727..80365832, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (80849728..80849833, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (79661546..79661651, complement)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene heterogeneous nuclear ribonucleoprotein A1 pseudogene 12 Neighboring gene mediator complex subunit 27 pseudogene Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:79703845-79704643 Neighboring gene zinc finger FYVE-type containing 16 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16139 Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:79783523-79784024 Neighboring gene FAM151B divergent transcript Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:79784025-79784524 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr5:79789343-79789929 Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:79793017-79793517 Neighboring gene family with sequence similarity 151 member B Neighboring gene RPS27A pseudogene 9

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_043278.1 

    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_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    80365727..80365832 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    80849728..80849833 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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