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PMS2P3 PMS1 homolog 2, mismatch repair system component pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 5387, updated on 4-Jun-2020

Summary

Official Symbol
PMS2P3provided by HGNC
Official Full Name
PMS1 homolog 2, mismatch repair system component pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:9128
See related
Ensembl:ENSG00000127957
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
PMS5; PMSR3; PMS2L3; PMS2L9
Expression
Ubiquitous expression in spleen (RPKM 4.3), testis (RPKM 4.0) and 25 other tissues See more

Genomic context

See PMS2P3 in Genome Data Viewer
Location:
7q11.23
Exon count:
9
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 7 NC_000007.14 (75507747..75528123, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (75137069..75157453, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene 7q11.23 proximal recombination region Neighboring gene POM121 transmembrane nucleoporin C Neighboring gene speedy/RINGO cell cycle regulator family member E5 Neighboring gene Sharpr-MPRA regulatory region 5953 Neighboring gene huntingtin interacting protein 1 Neighboring gene C-C motif chemokine ligand 26

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Markers

Other Names

  • postmeiotic segregation increased 2 pseudogene 3
  • postmeiotic segregation increased 2-like 3, pseudogene
  • postmeiotic segregation increased 2-like 9

Clone Names

  • MGC126647

Gene Ontology Provided by GOA

Function Evidence Code Pubs
ATPase activity IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
molecular_function ND
No biological Data available
more info
 
nucleic acid binding IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
biological_process ND
No biological Data available
more info
 
mismatch repair IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
regulation of transcription, DNA-templated IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
cellular_component ND
No biological Data available
more info
 
mismatch repair complex IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 

NCBI Reference Sequences (RefSeq)

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_028059.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC211429, BC007683
    Related
    ENST00000418756.5

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p13 Primary Assembly

    Range
    75507747..75528123 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001003686.1: Suppressed sequence

    Description
    NM_001003686.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
  2. NM_005395.2: Suppressed sequence

    Description
    NM_005395.2: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
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