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

Gene ID: 100151666, updated on 12-Oct-2019

Summary

Official Symbol
RNU7-69Pprovided by HGNC
Official Full Name
RNA, U7 small nuclear 69 pseudogeneprovided by HGNC
Primary source
HGNC: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

Genomic context

See RNU7-69P in Genome Data Viewer
Location:
Xq25
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (123772080..123772137, complement)
105 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 2 Neighboring gene FER tyrosine kinase pseudogene 1 Neighboring gene mediator of cell motility 1 pseudogene 4 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

General gene information

Markers

NCBI Reference Sequences (RefSeq)

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: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

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