Format

Send to:

Choose Destination

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

Gene ID: 106479520, updated on 23-Nov-2021

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
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See RN7SL818P in Genome Data Viewer
Location:
Yq11.23
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) Y NC_000024.10 (24210958..24211216, complement)
105.20201022 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)

NEW Try the new Transcript table

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
    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_000024.10 Reference GRCh38.p13 Primary Assembly

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