U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

RPL23AP82 ribosomal protein L23a pseudogene 82 [ Homo sapiens (human) ]

Gene ID: 284942, updated on 25-Oct-2022

Summary

Official Symbol
RPL23AP82provided by HGNC
Official Full Name
ribosomal protein L23a pseudogene 82provided by HGNC
Primary source
HGNC:HGNC:33730
See related
Ensembl:ENSG00000291064 AllianceGenome:HGNC:33730
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
RPL23A_43_1761
Expression
Ubiquitous expression in fat (RPKM 9.9), brain (RPKM 9.9) and 25 other tissues See more
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See RPL23AP82 in Genome Data Viewer
Location:
22q13.33
Exon count:
5
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (50757086..50799637)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (51270584..51313167)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (51195514..51238065)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene acrosin Neighboring gene small nuclear ribonucleoprotein polypeptide A' pseudogene Neighboring gene RAB, member of RAS oncogene family like 2B

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_026981.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    BC065556, BQ668440
  2. NR_026982.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks two 5' exons and contains an alternate exon, compared to variant 1.
    Source sequence(s)
    BC065556, DC308368
    Related
    ENST00000651346.2

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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    50757086..50799637
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    51270584..51313167
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_203302.2: Suppressed sequence

    Description
    NM_203302.2: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
  2. NM_203477.1: Suppressed sequence

    Description
    NM_203477.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.