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RN7SL823P RNA, 7SL, cytoplasmic 823, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479522, updated on 23-Nov-2021

Summary

Official Symbol
RN7SL823Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 823, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46839
See related
Ensembl:ENSG00000263595
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 RN7SL823P in Genome Data Viewer
Location:
19p13.11
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 19 NC_000019.10 (16910497..16910784, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (17021307..17021594, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene C3 and PZP like alpha-2-macroglobulin domain containing 8 Neighboring gene F2R like thrombin or trypsin receptor 3 Neighboring gene RNA, 7SL, cytoplasmic 835, pseudogene Neighboring gene Sharpr-MPRA regulatory region 9643 Neighboring gene HAUS augmin like complex subunit 8 Neighboring gene myosin IXB Neighboring gene small nucleolar RNA, H/ACA box 118

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_045747.1 

    Range
    101..388
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    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_000019.10 Reference GRCh38.p13 Primary Assembly

    Range
    16910497..16910784 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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