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RNA5SP276 RNA, 5S ribosomal pseudogene 276 [ Homo sapiens (human) ]

Gene ID: 100873529, updated on 10-Oct-2023

Summary

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Official Symbol
RNA5SP276provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 276provided by HGNC
Primary source
HGNC:HGNC:43176
See related
Ensembl:ENSG00000199450 AllianceGenome:HGNC:43176
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
RN5S276
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Genomic context

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Location:
8q23.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (116022686..116022779, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (117149871..117149964, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (117034911..117035004, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986902 Neighboring gene uncharacterized LOC107986903 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:116981560-116982759 Neighboring gene long intergenic non-protein coding RNA 536 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:117041007-117041189 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:117050679-117051374 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:117081592-117081754 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:117101307-117101884 Neighboring gene NANOG hESC enhancer GRCh37_chr8:117108567-117109155 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:117140378-117141004 Neighboring gene NANOG hESC enhancer GRCh37_chr8:117243536-117244062 Neighboring gene Sharpr-MPRA regulatory region 9276 Neighboring gene uncharacterized LOC124902005 Neighboring gene uncharacterized LOC102723447

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • RNA, 5S ribosomal 276

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_033350.1 

    Range
    101..194
    Download
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    116022686..116022779 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    117149871..117149964 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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