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RNU6-21P RNA, U6 small nuclear 21, pseudogene [ Homo sapiens (human) ]

Gene ID: 100302738, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-21Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 21, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:34265
See related
Ensembl:ENSG00000207441 AllianceGenome:HGNC:34265
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RNU6-21
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Genomic context

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Location:
16q21
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (62187540..62187646, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (67975308..67975414, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (62221444..62221550, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124903777 Neighboring gene NANOG hESC enhancer GRCh37_chr16:62078473-62078974 Neighboring gene uncharacterized LOC124903778 Neighboring gene small nucleolar RNA U13 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr16:62484136-62484802 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr16:62511246-62511746 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr16:62541865-62542411 Neighboring gene ReSE screen-validated silencer GRCh37_chr16:62629203-62629374 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr16:62699049-62699701 Neighboring gene uncharacterized LOC105371306

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)

See Variation Viewer (GRCh38)

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_044052.1 

    Range
    101..207
    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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    62187540..62187646 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    67975308..67975414 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Chemical Information
Molecular Biology Databases