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RNA5SP457 RNA, 5S ribosomal pseudogene 457 [ Homo sapiens (human) ]

Gene ID: 100873702, updated on 13-May-2022

Summary

Official Symbol
RNA5SP457provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 457provided by HGNC
Primary source
HGNC:HGNC:43357
See related
Ensembl:ENSG00000200527 AllianceGenome:HGNC:43357
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
RN5S457
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Genomic context

See RNA5SP457 in Genome Data Viewer
Location:
18q21.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (49946266..49946389, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (50148001..50148124, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (47472636..47472759, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene small Cajal body-specific RNA 17 Neighboring gene small nucleolar RNA host gene 22 Neighboring gene myosin VB Neighboring gene Sharpr-MPRA regulatory region 7262 Neighboring gene uncharacterized LOC124904299 Neighboring gene adenosine deaminase domain containing 1 pseudogene 2

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_033676.1 

    Range
    101..224
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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
    49946266..49946389 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    50148001..50148124 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)