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RPS24P14 ribosomal protein S24 pseudogene 14 [ Homo sapiens (human) ]

Gene ID: 100128423, updated on 17-Sep-2024

Summary

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Official Symbol
RPS24P14provided by HGNC
Official Full Name
ribosomal protein S24 pseudogene 14provided by HGNC
Primary source
HGNC:HGNC:35744
See related
AllianceGenome:HGNC:35744
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
RPS24_4_1115
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Genomic context

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See RPS24P14 in Genome Data Viewer
Location:
11p15.4
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (3559512..3560024)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (3604974..3605486)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (3580742..3581254)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101927708 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:3555923-3556422 Neighboring gene small nuclear ribonucleoprotein polypeptide C pseudogene 5 Neighboring gene serine/arginine-rich splicing factor SR45-like Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4309 Neighboring gene RPS3A pseudogene 39 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3080 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr11:3604611-3605252 Neighboring gene VPS51 pseudogene 5 Neighboring gene olfactory receptor family 7 subfamily E member 117 pseudogene

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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Markers

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_009035.2 

    Range
    101..613
    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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    3559512..3560024
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    3604974..3605486
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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