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RN7SL697P RNA, 7SL, cytoplasmic 697, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480526, updated on 13-May-2022

Summary

Official Symbol
RN7SL697Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 697, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46713
See related
Ensembl:ENSG00000264484 AllianceGenome:HGNC:46713
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 RN7SL697P in Genome Data Viewer
Location:
Xq28
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (154495815..154496113, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (152732335..152732633, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (153724165..153724463, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ubiquitin like 4A Neighboring gene solute carrier family 10 member 3 Neighboring gene FAM3 metabolism regulating signaling molecule A Neighboring gene uncharacterized LOC124905229 Neighboring gene Sharpr-MPRA regulatory region 11639

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_044023.1 

    Range
    101..399
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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
    154495815..154496113 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    152732335..152732633 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)