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RPS4XP21 ribosomal protein S4X pseudogene 21 [ Homo sapiens (human) ]

Gene ID: 126235, updated on 2-Nov-2024

Summary

Official Symbol
RPS4XP21provided by HGNC
Official Full Name
ribosomal protein S4X pseudogene 21provided by HGNC
Primary source
HGNC:HGNC:36228
See related
Ensembl:ENSG00000186008 AllianceGenome:HGNC:36228
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
RPS4P21; RPS4X_10_1649
Summary
Predicted to be located in nucleolus. Predicted to be part of cytosolic small ribosomal subunit. [provided by Alliance of Genome Resources, Nov 2024]
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Genomic context

See RPS4XP21 in Genome Data Viewer
Location:
19q13.11
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (34092476..34093361, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (36613125..36614010, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (34583381..34584266, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene ReSE screen-validated silencer GRCh37_chr19:34521753-34521905 Neighboring gene ribosomal protein S4X pseudogene 23 Neighboring gene ribosomal protein S4X pseudogene 20 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_51262 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:34617551-34618060 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 10501 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:34625657-34626192 Neighboring gene coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 3 Neighboring gene LSM14A mRNA processing body assembly factor Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr19:34715679-34716244

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_009255.3 

    Range
    101..986
    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_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    34092476..34093361 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    36613125..36614010 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)