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RN7SL168P RNA, 7SL, cytoplasmic 168, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480491, updated on 13-May-2022

Summary

Official Symbol
RN7SL168Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 168, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46184
See related
Ensembl:ENSG00000244296 AllianceGenome:HGNC:46184
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 RN7SL168P in Genome Data Viewer
Location:
22q11.21
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (19365765..19366044)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (19742475..19742754)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (19353288..19353567)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene clathrin heavy chain like 1 Neighboring gene keratin 18 pseudogene 62 Neighboring gene uncharacterized LOC105372859 Neighboring gene histone cell cycle regulator Neighboring gene mitochondrial ribosomal protein L40 Neighboring gene chromosome 22 open reading frame 39

Genomic regions, transcripts, and products

Pathways from PubChem

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_043768.1 

    Range
    101..380
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    19365765..19366044
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    19742475..19742754
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)