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RNU6-1323P RNA, U6 small nuclear 1323, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481598, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-1323Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1323, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48286
See related
Ensembl:ENSG00000206752 AllianceGenome:HGNC:48286
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:
Xq23
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (116850840..116850945, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (115227471..115227576, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (115984808..115984913, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105373320 Neighboring gene PRPF4B pseudogene 1 Neighboring gene uncharacterized LOC100126447 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:115946212-115946988 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:115950867-115951670 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:115951671-115952473 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:116065040-116065548 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:116065549-116066057 Neighboring gene Sharpr-MPRA regulatory region 1920 Neighboring gene SET pseudogene 8 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chrX:116381582-116382781 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:116414963-116415464 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:116415465-116415964 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:116438886-116439386 Neighboring gene TCERG1 pseudogene 1

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_044413.1 

    Range
    101..206
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    116850840..116850945 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    115227471..115227576 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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