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RNA5SP522 RNA, 5S ribosomal pseudogene 522 [ Homo sapiens (human) ]

Gene ID: 106479019, updated on 10-Oct-2023

Summary

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Official Symbol
RNA5SP522provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 522provided by HGNC
Primary source
HGNC:HGNC:43422
See related
AllianceGenome:HGNC:43422
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
RN5S522
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Genomic context

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Location:
Yq11.222
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (18346023..18346338, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (19252511..19252826, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (20507909..20508224, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene clustered mitochondria homolog pseudogene 2 Neighboring gene family with sequence similarity 224 member A Neighboring gene uncharacterized LOC105377220 Neighboring gene RNA, 5S ribosomal pseudogene 523 Neighboring gene tubulin beta 1 class VI pseudogene 1 Neighboring gene family with sequence similarity 41 member A, Y-linked 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)

General gene information

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Other Names

  • RNA, 5S ribosomal 522

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_084007.1 

    Range
    101..416
    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_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    18346023..18346338 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    19252511..19252826 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_044243.1: Suppressed sequence

    Description
    NG_044243.1: This RefSeq was permanently suppressed because this pseudogene is now annotated on NG_004636.1
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Molecular Biology Databases