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RN7SL818P RNA, 7SL, cytoplasmic 818, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479520, updated on 10-Oct-2023

Summary

Official Symbol
RN7SL818Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 818, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46834
See related
Ensembl:ENSG00000274234 AllianceGenome:HGNC:46834
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

Location:
Yq11.23
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (24210958..24211216, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (24651361..24651619)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (26357105..26357363, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene CSPG4 pseudogene 2 Y-linked Neighboring gene CSPG4 pseudogene 3 Y-linked Neighboring gene CHRFAM7A pseudogene 2 Neighboring gene GOLGA2 pseudogene 2 Y-linked Neighboring gene UBE2Q2 pseudogene 4, Y-linked Neighboring gene dynamin 1 pseudogene 25

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_045740.1 

    Range
    101..359
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    24210958..24211216 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    24651361..24651619
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)