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RNA5SP529 RNA, 5S ribosomal pseudogene 529 [ Homo sapiens (human) ]

Gene ID: 111644136, updated on 17-Sep-2024

Summary

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Official Symbol
RNA5SP529provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 529provided by HGNC
Primary source
HGNC:HGNC:53798
See related
Ensembl:ENSG00000276442 AllianceGenome:HGNC:53798
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See RNA5SP529 in Genome Data Viewer
Location:
1q21.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (144265217..144265326)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (143800770..143800879, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 (PATCHES) NW_003871055.3 (1080630..1080739)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene proton channel OTOP1-like Neighboring gene long intergenic non-protein coding RNA 2802 Neighboring gene Sharpr-MPRA regulatory region 154 duplicate 2 Neighboring gene D(1B) dopamine receptor-like Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:148864647-148865255 Neighboring gene extensin Neighboring gene Sharpr-MPRA regulatory region 1883 duplicate 2

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)

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_056349.1 

    Range
    101..210
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    144265217..144265326
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    143800770..143800879 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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