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RN7SL164P RNA, 7SL, cytoplasmic 164, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480965, updated on 25-Jan-2022

Summary

Official Symbol
RN7SL164Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 164, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46180
See related
Ensembl:ENSG00000242614 AllianceGenome:HGNC:46180
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 RN7SL164P in Genome Data Viewer
Location:
13q32.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 13 NC_000013.11 (96169545..96169847)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (96821799..96822101)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370322 Neighboring gene high mobility group nucleosome binding domain 1 pseudogene 24 Neighboring gene UDP-glucose glycoprotein glucosyltransferase 2 Neighboring gene heparan sulfate 6-O-sulfotransferase 3 Neighboring gene microRNA 4501 Neighboring gene AMMECR1 like 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_045466.1 

    Range
    101..403
    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_000013.11 Reference GRCh38.p13 Primary Assembly

    Range
    96169545..96169847
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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