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RN7SL217P RNA, 7SL, cytoplasmic 217, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479301, updated on 23-Nov-2021

Summary

Official Symbol
RN7SL217Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 217, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46233
See related
Ensembl:ENSG00000264706
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 RN7SL217P in Genome Data Viewer
Location:
3p21.31
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (49863375..49863660, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (49900808..49901093, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 10954 Neighboring gene microRNA 5193 Neighboring gene ubiquitin like modifier activating enzyme 7 Neighboring gene TRAF interacting protein Neighboring gene CaM kinase like vesicle associated Neighboring gene actin like 11, pseudogene Neighboring gene macrophage stimulating 1 receptor Neighboring gene uncharacterized LOC102724438

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_045858.1 

    Range
    101..386
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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_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    49863375..49863660 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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