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RNU6ATAC23P RNA, U6atac small nuclear 23, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481166, updated on 13-May-2022

Summary

Official Symbol
RNU6ATAC23Pprovided by HGNC
Official Full Name
RNA, U6atac small nuclear 23, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46922
See related
Ensembl:ENSG00000221375 AllianceGenome:HGNC:46922
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 RNU6ATAC23P in Genome Data Viewer
Location:
Xq27.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (139885481..139885603)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (138197403..138197525)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (138967640..138967762)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene MCF.2 cell line derived transforming sequence Neighboring gene small nucleolar RNA U13 Neighboring gene brain cytoplasmic RNA 1, pseudogene 1 Neighboring gene ATPase phospholipid transporting 11C Neighboring gene microRNA 505 Neighboring gene chromosome X open reading frame 66

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_043019.1 

    Range
    101..223
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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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    139885481..139885603
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    138197403..138197525
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)