PRRX2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Paired mesoderm homeobox protein 2 is a protein that in humans is encoded by the PRRX2 gene.[5][6]

AliasesPRRX2, PMX2, PRX2, paired related homeobox 2
End129,722,674 bp[1]
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PRRX2
Identifiers
AliasesPRRX2, PMX2, PRX2, paired related homeobox 2
External IDsOMIM: 604675; MGI: 98218; HomoloGene: 7524; GeneCards: PRRX2; OMA:PRRX2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_016307

NM_009116

RefSeq (protein)

NP_057391

NP_033142

Location (UCSC)Chr 9: 129.67 – 129.72 MbChr 2: 30.72 – 30.77 Mb
PubMed search[3][4]
Wikidata
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Function

The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins. Expression is localized to proliferating fetal fibroblasts and the developing dermal layer, with downregulated expression in adult skin. Increases in expression of this gene during fetal but not adult wound healing suggest a possible role in mechanisms that control mammalian dermal regeneration and prevent formation of scar response to wounding. The expression patterns provide evidence consistent with a role in fetal skin development and a possible role in cellular proliferation.[6]

References

Further reading

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