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RN7SL38P RNA, 7SL, cytoplasmic 38, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480932, updated on 23-Nov-2021

Summary

Official Symbol
RN7SL38Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 38, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46054
See related
Ensembl:ENSG00000240481
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 RN7SL38P in Genome Data Viewer
Location:
12p12.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (24706788..24707076)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (24859722..24860010)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 477 Neighboring gene lysine rich nucleolar protein 1 pseudogene 1 Neighboring gene uncharacterized LOC105369698 Neighboring gene ribosomal protein L21 pseudogene 102 Neighboring gene uncharacterized LOC105369699 Neighboring gene branched chain amino acid transaminase 1 Neighboring gene defender against cell death 1 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_043204.1 

    Range
    101..389
    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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    24706788..24707076
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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