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RPL4P2 ribosomal protein L4 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 646688, updated on 17-Sep-2024

Summary

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Official Symbol
RPL4P2provided by HGNC
Official Full Name
ribosomal protein L4 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:36836
See related
Ensembl:ENSG00000232341 AllianceGenome:HGNC:36836
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
RPL4_1_115
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Genomic context

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See RPL4P2 in Genome Data Viewer
Location:
1q24.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (166747323..166748749)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (166093164..166094589)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (166716560..166717986)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene flavin containing dimethylaniline monoxygenase 9, pseudogene Neighboring gene flavin containing dimethylaniline monoxygenase 10, pseudogene Neighboring gene MED14-independent group 3 enhancer GRCh37_chr1:166644091-166645290 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:166687833-166687935 Neighboring gene flavin containing dimethylaniline monoxygenase 11, pseudogene Neighboring gene MPRA-validated peak440 silencer Neighboring gene calponin 2 pseudogene 10

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_010174.1 

    Range
    101..1527
    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    166747323..166748749
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    166093164..166094589
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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