Gene Expression Literature Summary

• Symbol: Ptges3
• Name: prostaglandin E synthase 3
• ID: MGI:1929282

5 matching records from 5 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.

Age	E9.5	E10.5	E18.5	P
Immunohistochemistry (section)			1
In situ RNA (whole mount)	1	1
Northern blot			1
Western blot			4	1

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available

Ptges3  prostaglandin E synthase 3   (Synonyms: 5730442A20Rik, cPGES, p23 cochaperone, Ptges, sid3177, Tebp)
Results	Reference
2	J:89946 Bush JO, Lan Y, Jiang R, The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene. Proc Natl Acad Sci U S A. 2004 May 4;101(18):7022-7
2*	J:267157 Flaveny C, Perdew GH, Miller CA 3rd, The Aryl-hydrocarbon receptor does not require the p23 co-chaperone for ligand binding and target gene expression in vivo. Toxicol Lett. 2009 Aug 25;189(1):57-62
1*	J:117591 Grad I, McKee TA, Ludwig SM, Hoyle GW, Ruiz P, Wurst W, Floss T, Miller CA 3rd, Picard D, The Hsp90 cochaperone p23 is essential for perinatal survival. Mol Cell Biol. 2006 Dec;26(23):8976-83
2*	J:122356 Lovgren AK, Kovarova M, Koller BH, cPGES/p23 is required for glucocorticoid receptor function and embryonic growth but not prostaglandin E2 synthesis. Mol Cell Biol. 2007 Jun;27(12):4416-30
2*	J:245622 Madon-Simon M, Grad I, Bayo P, Perez P, Picard D, Defective glucocorticoid receptor signaling and keratinocyte-autonomous defects contribute to skin phenotype of mouse embryos lacking the Hsp90 co-chaperone p23. PLoS One. 2017;12(6):e0180035