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RN7SL220P RNA, 7SL, cytoplasmic 220, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479303, updated on 23-Nov-2021

Summary

Official Symbol
RN7SL220Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 220, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46236
See related
Ensembl:ENSG00000266467
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 RN7SL220P in Genome Data Viewer
Location:
10q21.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (68007718..68008017, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (69767475..69767774, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene SIRT1 promoter region Neighboring gene sirtuin 1 Neighboring gene HECT and RLD domain containing E3 ubiquitin protein ligase 4 Neighboring gene RPS3A pseudogene 38 Neighboring gene POU class 5 homeobox 1 pseudogene 5 Neighboring gene myopalladin Neighboring gene uncharacterized LOC107984240 Neighboring gene RN7SK pseudogene 202

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_045864.1 

    Range
    101..400
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    68007718..68008017 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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