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RPS15AP40 ribosomal protein S15a pseudogene 40 [ Homo sapiens (human) ]

Gene ID: 100128083, updated on 11-Jun-2021

Summary

Official Symbol
RPS15AP40provided by HGNC
Official Full Name
ribosomal protein S15a pseudogene 40provided by HGNC
Primary source
HGNC:HGNC:36041
See related
Ensembl:ENSG00000233921
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
RPS15A_26_1770
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Genomic context

See RPS15AP40 in Genome Data Viewer
Location:
Xp21.1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (36374755..36375213, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (36392870..36393328, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene cilia and flagella associated protein 47 Neighboring gene RNA, U6 small nuclear 641, pseudogene Neighboring gene high mobility group box 1 pseudogene 16 Neighboring gene uncharacterized LOC101928627 Neighboring gene uncharacterized LOC105373155 Neighboring gene H2A.L variant histone 1Q, pseudogene Neighboring gene myosin heavy chain IB

Genomic regions, transcripts, and products

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_010442.1 

    Range
    101..559
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    36374755..36375213 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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