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RN7SL754P RNA, 7SL, cytoplasmic 754, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479497, updated on 23-Nov-2021

Summary

Official Symbol
RN7SL754Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 754, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46770
See related
Ensembl:ENSG00000239822
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 RN7SL754P in Genome Data Viewer
Location:
10p15.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (430239..430504, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (476179..476444, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene RNA, 5S ribosomal pseudogene 298 Neighboring gene disco interacting protein 2 homolog C Neighboring gene uncharacterized LOC105376340 Neighboring gene nonconserved acetylation island sequence 51 enhancer Neighboring gene uncharacterized LOC101930421

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_045667.1 

    Range
    101..366
    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_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    430239..430504 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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