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RPS2P32 ribosomal protein S2 pseudogene 32 [ Homo sapiens (human) ]

Gene ID: 256355, updated on 13-May-2022

Summary

Official Symbol
RPS2P32provided by HGNC
Official Full Name
ribosomal protein S2 pseudogene 32provided by HGNC
Primary source
HGNC:HGNC:30518
See related
Ensembl:ENSG00000232818 AllianceGenome:HGNC:30518
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RPS2_14_794
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Genomic context

See RPS2P32 in Genome Data Viewer
Location:
7p15.3
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (23490388..23491428)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (23626796..23627836)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (23530007..23531047)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene insulin like growth factor 2 mRNA binding protein 3 Neighboring gene RNA, U7 small nuclear 143 pseudogene Neighboring gene chromosome 5 open reading frame 13 pseudogene Neighboring gene transformer 2 alpha homolog Neighboring gene ATP binding cassette subfamily E member 1 pseudogene

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.

RNA

  1. NR_026676.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC023105
    Related
    ENST00000439199.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    23490388..23491428
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    23626796..23627836
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_005656.3: Suppressed sequence

    Description
    NG_005656.3: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene.