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RNU6-409P RNA, U6 small nuclear 409, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481307, updated on 13-May-2022

Summary

Official Symbol
RNU6-409Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 409, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47372
See related
Ensembl:ENSG00000206841 AllianceGenome:HGNC:47372
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

See RNU6-409P in Genome Data Viewer
Location:
22q13.33
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (50691260..50691363, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (51204551..51204654, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (51129688..51129791, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124905149 Neighboring gene arylsulfatase A Neighboring gene SH3 and multiple ankyrin repeat domains 3 Neighboring gene uncharacterized LOC105373100 Neighboring gene acrosin

Genomic regions, transcripts, and products

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_044133.1 

    Range
    101..204
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    50691260..50691363 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_015148969.2 Reference GRCh38.p14 PATCHES

    Range
    27174..27277 complement
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    51204551..51204654 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)