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RPL23P10 ribosomal protein L23 pseudogene 10 [ Homo sapiens (human) ]

Gene ID: 100270962, updated on 10-Oct-2023

Summary

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Official Symbol
RPL23P10provided by HGNC
Official Full Name
ribosomal protein L23 pseudogene 10provided by HGNC
Primary source
HGNC:HGNC:36177
See related
Ensembl:ENSG00000244708 AllianceGenome:HGNC:36177
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
RPL23_2_893
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Genomic context

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See RPL23P10 in Genome Data Viewer
Location:
8p12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (36581197..36581588, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (36857256..36857647, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (36438715..36439106, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene MT-ND5 pseudogene 41 Neighboring gene RNA, U6 small nuclear 533, pseudogene Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:36251221-36251872 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr8:36347406-36348605 Neighboring gene OCT4-H3K27ac hESC enhancer GRCh37_chr8:36483643-36484316 Neighboring gene MPRA-validated peak6993 silencer Neighboring gene RNA, 5S ribosomal pseudogene 264 Neighboring gene mitochondrial ribosomal protein S7 pseudogene 1 Neighboring gene potassium calcium-activated channel subfamily U member 1

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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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_010585.1 

    Range
    101..492
    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
    36581197..36581588 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    36857256..36857647 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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