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RN7SL792P RNA, 7SL, cytoplasmic 792, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479509, updated on 25-Jan-2022

Summary

Official Symbol
RN7SL792Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 792, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46808
See related
Ensembl:ENSG00000239888 AllianceGenome:HGNC:46808
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 RN7SL792P in Genome Data Viewer
Location:
17p12
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (15408384..15408688)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (15311701..15312005)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene peripheral myelin protein 22 Neighboring gene microRNA 4731 Neighboring gene RNA, U6 small nuclear 799, pseudogene Neighboring gene tektin 3 Neighboring gene TVP23C-CDRT4 readthrough Neighboring gene CMT1A duplicated region transcript 4 Neighboring gene ribosomal protein L9 pseudogene 2 Neighboring gene CMT1A duplicated region transcript 3

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_044080.1 

    Range
    101..405
    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_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    15408384..15408688
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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