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RPL19P21 ribosomal protein L19 pseudogene 21 [ Homo sapiens (human) ]

Gene ID: 392557, updated on 10-Oct-2023

Summary

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Official Symbol
RPL19P21provided by HGNC
Official Full Name
ribosomal protein L19 pseudogene 21provided by HGNC
Primary source
HGNC:HGNC:35868
See related
Ensembl:ENSG00000230508 AllianceGenome:HGNC:35868
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
RPL19_13_1819
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Genomic context

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See RPL19P21 in Genome Data Viewer
Location:
Xq28
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (150993465..150994175)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (149260933..149261643)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (150161938..150162648)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 383, pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:150136026-150136543 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:150150822-150151517 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 21055 Neighboring gene high mobility group box 3 Neighboring gene ribosomal protein L12 pseudogene 50 Neighboring gene RNA, 5S ribosomal pseudogene 525

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_010567.2 

    Range
    101..811
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    150993465..150994175
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    149260933..149261643
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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