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RN7SL472P RNA, 7SL, cytoplasmic 472, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479395, updated on 20-Mar-2020

Summary

Official Symbol
RN7SL472Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 472, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46488
See related
Ensembl:ENSG00000240457
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See RN7SL472P in Genome Data Viewer
Location:
14q32.31
Annotation release Status Assembly Chr Location
109.20200228 current GRCh38.p13 (GCF_000001405.39) 14 NC_000014.9 (102077180..102077469, complement)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene protein phosphatase 2 regulatory subunit B'gamma Neighboring gene nucleophosmin 1 pseudogene 20 Neighboring gene dynein cytoplasmic 1 heavy chain 1 Neighboring gene uncharacterized LOC107984661 Neighboring gene heat shock protein 90 alpha family class A member 1 Neighboring gene WD repeat domain 20 Neighboring gene uncharacterized LOC105370677

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000014.9 Chromosome 14 Reference GRCh38.p13 Primary Assembly

NCBI Reference Sequences (RefSeq)

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_043192.1 

    Range
    101..390
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p13 Primary Assembly

    Range
    102077180..102077469 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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