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RPS5P8 RPS5 pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 392424, updated on 17-Sep-2024

Summary

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Official Symbol
RPS5P8provided by HGNC
Official Full Name
RPS5 pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:36531
See related
Ensembl:ENSG00000237730 AllianceGenome:HGNC:36531
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
RPS5_5_1762
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Genomic context

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See RPS5P8 in Genome Data Viewer
Location:
Xp22.31
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (6422047..6422773, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (5974353..5975079, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (6340088..6340814, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene neuroligin 4 X-linked Neighboring gene uncharacterized LOC105373156 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:6194636-6195374 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:6197302-6198185 Neighboring gene microRNA 4770 Neighboring gene S232-VCX3A recombination region Neighboring gene uncharacterized LOC124905240 Neighboring gene variable charge X-linked 3A

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Comparative analysis of processed ribosomal protein pseudogenes in four mammalian genomes. Balasubramanian S, et al. Genome Biol, 2009. PMID 19123937, Free PMC Article

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

  • ribosomal protein S5 pseudogene 8

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_011198.1 

    Range
    101..827
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    6422047..6422773 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    5974353..5975079 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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