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RN7SL197P RNA, 7SL, cytoplasmic 197, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480975, updated on 23-Nov-2021

Summary

Official Symbol
RN7SL197Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 197, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46213
See related
Ensembl:ENSG00000276031
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 RN7SL197P in Genome Data Viewer
Location:
20q13.13
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 20 NC_000020.11 (49721949..49722247)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (48338486..48338784)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105372651 Neighboring gene beta-1,4-galactosyltransferase 5 Neighboring gene Sharpr-MPRA regulatory region 2374 Neighboring gene small nuclear ribonucleoprotein polypeptide F pseudogene 1 Neighboring gene uncharacterized LOC105372652

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_043559.1 

    Range
    101..399
    Download
    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_000020.11 Reference GRCh38.p13 Primary Assembly

    Range
    49721949..49722247
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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