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RPL31P4 ribosomal protein L31 pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 729646, updated on 4-Mar-2025

Summary

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Official Symbol
RPL31P4provided by HGNC
Official Full Name
ribosomal protein L31 pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:23546
See related
Ensembl:ENSG00000213598 AllianceGenome:HGNC:23546
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
RPL31_28_1375
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Genomic context

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See RPL31P4 in Genome Data Viewer
Location:
14q23.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (58794630..58795071)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (53001779..53002220)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (59261348..59261789)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5801 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:59129886-59130387 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:59130388-59130888 Neighboring gene dishevelled binding antagonist of beta catenin 1 Neighboring gene uncharacterized LOC102723725 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:59218720-59219442 Neighboring gene Sharpr-MPRA regulatory region 9975 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr14:59235232-59235813 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr14:59235814-59236394 Neighboring gene transmembrane protein 98 pseudogene Neighboring gene long intergenic non-protein coding RNA 1500 Neighboring gene NANOG hESC enhancer GRCh37_chr14:59313280-59313820 Neighboring gene uncharacterized LOC124903325

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_009376.1 

    Range
    101..542
    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_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    58794630..58795071
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    53001779..53002220
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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