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RNU7-69P RNA, U7 small nuclear 69 pseudogene [ Homo sapiens (human) ]

Gene ID: 100151666, updated on 10-Oct-2023

Summary

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Official Symbol
RNU7-69Pprovided by HGNC
Official Full Name
RNA, U7 small nuclear 69 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:34165
See related
Ensembl:ENSG00000252178 AllianceGenome:HGNC:34165
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
U7.69
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Genomic context

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Location:
Xq25
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (123772080..123772137, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (122082514..122082571, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (122905930..122905987, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene THO complex subunit 2 Neighboring gene FER tyrosine kinase pseudogene 1 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:122781620-122782478 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:122782479-122783335 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:122813879-122814524 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29909 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:122911827-122912619 Neighboring gene MEMO1 pseudogene 4 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29910 Neighboring gene coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 1 Neighboring gene RNA, 7SL, cytoplasmic 190, pseudogene

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. U7 snRNAs: a computational survey. Marz M, et al. Genomics Proteomics Bioinformatics, 2007 Dec. PMID 18267300, Free PMC Article

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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Markers

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_007685.1 

    Range
    101..158
    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
    123772080..123772137 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    122082514..122082571 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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