PTGER2: Prostaglandin E2 Receptor EP2 Subtype

GPCR Mediating PGE2 Signaling in Inflammation, Pain, and Cancer

Gene Information Card

Symbol PTGER2
Full Name Prostaglandin E2 Receptor EP2 Subtype
Gene Type protein-coding
Chromosomal Location 14q22.1
NCBI Gene ID 5732 ncbi.nlm.nih.gov/gene/5732
Ensembl ID ENSG00000125384
UniProt ID P43116
OMIM ID 176804
HGNC ID 9595
Aliases EP2, EP2R, PGE2 receptor EP2

Description

PTGER2 encodes the EP2 subtype of the prostaglandin E2 (PGE2) receptor, a G protein-coupled receptor (GPCR) that primarily couples to Gs alpha and stimulates cAMP production. It mediates diverse physiological and pathological processes including inflammation, pain, fever, bone metabolism, reproduction, and cancer progression. Activation of PTGER2 promotes vasodilation, bronchorelaxation, and immune modulation.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Inflammatory pain EP2 activation sensitizes nociceptors via cAMP-PKA pathway PMID: 19074568
Colorectal cancer PGE2-EP2 signaling promotes tumor growth via β-catenin activation PMID: 15619630
Endometriosis Elevated PTGER2 expression in endometriotic lesions PMID: 21900417
Asthma EP2 agonists induce bronchodilation; polymorphisms associated with airway hyperresponsiveness PMID: 12626338
Rheumatoid arthritis EP2 contributes to synovial inflammation and bone erosion PMID: 20037587

Expression Profile

Tissue Expression
Tissue nTPM level
Lung 12.3 Medium
Kidney 8.7 Medium
Spleen 6.5 Low
Small intestine 5.9 Low
Uterus 4.8 Low
Cell Line Expression
Cell Line nTPM Notes
A549 (lung carcinoma) 15.2 High expression
HEK293 (embryonic kidney) 9.1 Medium expression
HCT116 (colorectal carcinoma) 7.4 Medium expression
MCF7 (breast carcinoma) 3.6 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.665C>T (p.Pro222Leu) Missense <0.01% Unknown functional effect
c.1031G>A (p.Arg344His) Missense <0.01% Reported in ClinVar as uncertain significance
c.1246C>T (p.Arg416*) Nonsense <0.01% Predicted loss of function
Mutation functional classification

Loss of Function (LOF)

Nonsense mutations (e.g., p.Arg416*) likely cause truncated non-functional receptor.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in PTGER2.

Dominant Negative (DN)

No dominant-negative mutations described for PTGER2.

Gene Ontology (GO)

• G protein-coupled receptor activity • prostaglandin E2 receptor activity
• adenylate cyclase-activating G protein-coupled receptor signaling pathway • inflammatory response
• positive regulation of cAMP-mediated signaling • cell proliferation
• vasodilation

Pathways

GPCR downstream signaling (Gs-alpha/cAMP/PKA)
PGE2 signaling in inflammation
β-catenin activation in colorectal cancer
cAMP-mediated smooth muscle relaxation

Protein Summary

PTGER2 (EP2) is a 358-amino acid G protein-coupled receptor with seven transmembrane domains. It binds prostaglandin E2 with high affinity and couples to Gs alpha to increase intracellular cAMP. The receptor is expressed in multiple tissues including lung, kidney, and immune cells. EP2 plays key roles in inflammation, pain, and cancer, and is a target for therapeutic modulation in inflammatory diseases and oncology.

Related Products

Product name Cat.No. Species Gene ID
PTGER2 Knockout HEK293 Cell Line EDJ-KQ1768 Human 5732 Details Get a Quote
PTGER2 Knockout HCT 116 Cell Line EDJ-KQ21640 Human 5732 Details Get a Quote
PTGER2 Knockout HeLa Cell Line EDJ-KQ54257 Human 5732 Details Get a Quote
PTGER2 Knockout A-549 Cell Line EDJ-KQ62748 Human 5732 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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