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RNA5SP456 RNA, 5S ribosomal pseudogene 456 [ Homo sapiens (human) ]

Gene ID: 100873701, updated on 13-May-2022

Summary

Official Symbol
RNA5SP456provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 456provided by HGNC
Primary source
HGNC:HGNC:43356
See related
Ensembl:ENSG00000200872 AllianceGenome:HGNC:43356
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RN5S456
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Genomic context

See RNA5SP456 in Genome Data Viewer
Location:
18q21.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (48475487..48475600, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (48666291..48666404, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (46001858..46001971, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene zinc finger and BTB domain containing 7C Neighboring gene uncharacterized LOC124904353 Neighboring gene Sharpr-MPRA regulatory region 5458 Neighboring gene RNA polymerase III subunit G pseudogene 2 Neighboring gene cap binding complex dependent translation initiation factor Neighboring gene microRNA 4743

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_033674.1 

    Range
    101..214
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000018.10 Reference GRCh38.p14 Primary Assembly

    Range
    48475487..48475600 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    48666291..48666404 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)