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RPS3AP51 RPS3A pseudogene 51 [ Homo sapiens (human) ]

Gene ID: 100271600, updated on 13-May-2022

Summary

Official Symbol
RPS3AP51provided by HGNC
Official Full Name
RPS3A pseudogene 51provided by HGNC
Primary source
HGNC:HGNC:35480
See related
AllianceGenome:HGNC:35480
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
RPS3A_23_1744
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Genomic context

See RPS3AP51 in Genome Data Viewer
Location:
22q12.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (30136630..30137398, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (30599933..30600701, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (30532619..30533387, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene HORMAD2 and MTMR3 antisense RNA 1 Neighboring gene calponin 2 pseudogene 1 Neighboring gene HORMA domain containing 2 Neighboring gene ribosomal protein L36 pseudogene 17 Neighboring gene uncharacterized LOC105372988 Neighboring gene Sharpr-MPRA regulatory region 10236

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_011242.1 

    Range
    101..869
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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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    30136630..30137398 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    30599933..30600701 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)