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RPSAP59 ribosomal protein SA pseudogene 59 [ Homo sapiens (human) ]

Gene ID: 100271148, updated on 25-Jan-2022

Summary

Official Symbol
RPSAP59provided by HGNC
Official Full Name
ribosomal protein SA pseudogene 59provided by HGNC
Primary source
HGNC:HGNC:36957
See related
Ensembl:ENSG00000233071 AllianceGenome:HGNC:36957
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
RPSA_27_1799
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Genomic context

See RPSAP59 in Genome Data Viewer
Location:
Xq22.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (103206009..103206899, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (102460937..102461827, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 49 Neighboring gene brain expressed X-linked 1 Neighboring gene zinc finger protein 770 pseudogene Neighboring gene nuclear RNA export factor 3 Neighboring gene CRISPRi-validated cis-regulatory element chrX.1663 Neighboring gene brain expressed X-linked 4

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_010239.1 

    Range
    101..991
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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
    103206009..103206899 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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