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

Gene ID: 100873701, updated on 12-Oct-2019

Summary

Official Symbol
RNA5SP456provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 456provided by HGNC
Primary source
HGNC: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

Genomic context

See RNA5SP456 in Genome Data Viewer
Location:
18q21.1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 18 NC_000018.10 (48475487..48475600, complement)
105 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 chromosome 18 open reading frame 12 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 uncharacterized LOC107987258

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000018.10 Reference GRCh38.p13 Primary Assembly

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