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PRORSD1P prolyl-tRNA synthetase associated domain containing 1, pseudogene [ Homo sapiens (human) ]

Gene ID: 344405, updated on 13-May-2022

Summary

Official Symbol
PRORSD1Pprovided by HGNC
Official Full Name
prolyl-tRNA synthetase associated domain containing 1, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:34379
See related
Ensembl:ENSG00000162997 AllianceGenome:HGNC:34379
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ProX; Ybakd1; Prdxdd1; PRDXDD1P; ProXp-ala; NCRNA00117
Summary
Predicted to enable aminoacyl-tRNA editing activity. Predicted to be involved in aminoacyl-tRNA metabolism involved in translational fidelity. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See PRORSD1P in Genome Data Viewer
Location:
2p16.1
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (55282319..55284472)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (55279543..55281678)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (55509455..55511608)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene mitochondrial translational initiation factor 2 Neighboring gene Sharpr-MPRA regulatory regions 8685 and 822 Neighboring gene Sharpr-MPRA regulatory region 7699 Neighboring gene coiled-coil domain containing 88A Neighboring gene uncharacterized LOC124907768

Genomic regions, transcripts, and products

General gene information

Other Names

  • PrdX deacylase domain containing 1, pseudogene
  • YBak domain containing 1
  • prolyl-tRNA synthetase domain containing 1, pseudogene

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables aminoacyl-tRNA editing activity IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
involved_in aminoacyl-tRNA metabolism involved in translational fidelity IEA
Inferred from Electronic Annotation
more info
 

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.

RNA

  1. NR_027258.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC012358
    Related
    ENST00000563365.1

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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    55282319..55284472
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    55279543..55281678
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001080459.1: Suppressed sequence

    Description
    NM_001080459.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.