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RN7SL169P RNA, 7SL, cytoplasmic 169, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480372, updated on 11-Jun-2021

Summary

Official Symbol
RN7SL169Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 169, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46185
See related
Ensembl:ENSG00000242547
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 RN7SL169P in Genome Data Viewer
Location:
5q12.3
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 5 NC_000005.10 (64539505..64539789)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (63835332..63835616)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene 5-hydroxytryptamine receptor 1A Neighboring gene Sharpr-MPRA regulatory region 1263 Neighboring gene ring finger protein 180 Neighboring gene regulator of G protein signaling 7 binding protein Neighboring gene RNA, U6 small nuclear 294, pseudogene Neighboring gene mitochondrial ribosomal protein L49 pseudogene 1

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_046006.1 

    Range
    101..385
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000005.10 Reference GRCh38.p13 Primary Assembly

    Range
    64539505..64539789
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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