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RNU11-6P RNA, U11 small nuclear 6, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480544, updated on 10-Oct-2023

Summary

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Official Symbol
RNU11-6Pprovided by HGNC
Official Full Name
RNA, U11 small nuclear 6, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46946
See related
Ensembl:ENSG00000212429 AllianceGenome:HGNC:46946
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:
8q21.13
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (80749561..80749693, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (81181139..81181271, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (81661796..81661928, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene RNA, 7SL, cytoplasmic 107, pseudogene Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:81552571-81553770 Neighboring gene zinc finger protein 704 Neighboring gene CDC28 protein kinase regulatory subunit 1B pseudogene 7 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:81610513-81611014 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:81611015-81611514 Neighboring gene RNA, 7SL, cytoplasmic 308, pseudogene Neighboring gene high mobility group box 1 pseudogene 41

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_045741.1 

    Range
    101..233
    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
    80749561..80749693 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    81181139..81181271 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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