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RPSAP20 ribosomal protein SA pseudogene 20 [ Homo sapiens (human) ]

Gene ID: 127406, updated on 13-May-2022

Summary

Official Symbol
RPSAP20provided by HGNC
Official Full Name
ribosomal protein SA pseudogene 20provided by HGNC
Primary source
HGNC:HGNC:35595
See related
Ensembl:ENSG00000229871 AllianceGenome:HGNC:35595
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_1_53
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Genomic context

See RPSAP20 in Genome Data Viewer
Location:
1p32.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (56207472..56208529, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (56090464..56091521, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (56673144..56674201, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904187 Neighboring gene uncharacterized LOC124904190 Neighboring gene uncharacterized LOC124904186 Neighboring gene uncharacterized LOC124904185 Neighboring gene long intergenic non-protein coding RNA 1767

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_010906.3 

    Range
    101..1158
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    GenBank, FASTA, Sequence Viewer (Graphics)

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    56207472..56208529 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    56090464..56091521 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)