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RPS3AP5 RPS3A pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 439992, updated on 23-Nov-2021

Summary

Official Symbol
RPS3AP5provided by HGNC
Official Full Name
RPS3A pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:23744
See related
Ensembl:ENSG00000178429
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
bA486O22.3; RPS3A_15_1074
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Genomic context

See RPS3AP5 in Genome Data Viewer
Location:
10q23.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (84560419..84561306)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (86320175..86321062)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene coiled-coil serine rich protein 2 Neighboring gene transportin 1 pseudogene 1 Neighboring gene calcyclin binding protein pseudogene 1 Neighboring gene uncharacterized LOC105378400 Neighboring gene uncharacterized LOC105378401 Neighboring gene uncharacterized LOC107984249

Genomic regions, transcripts, and products

Phenotypes

Associated conditions

Description Tests
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
GeneReviews: Not available

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_009792.2 

    Range
    101..988
    Download
    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_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    84560419..84561306
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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