PTGER4 Gene (Prostaglandin E Receptor 4)

GPCR for PGE2 signaling in inflammation, immunity, and cancer

Gene Information Card

Symbol PTGER4
Full Name Prostaglandin E Receptor 4
Gene Type protein-coding
Chromosomal Location 5p13.1
NCBI Gene ID 5734 ncbi.nlm.nih.gov/gene/5734
Ensembl ID ENSG00000171522
UniProt ID P35408
OMIM ID 601586
HGNC ID 9596
Aliases EP4, EP4R, PGE2 receptor EP4 subtype

Description

PTGER4 encodes the prostaglandin E receptor subtype EP4, a G-protein-coupled receptor (GPCR) that binds prostaglandin E2 (PGE2). It activates Gs-mediated cAMP signaling and plays key roles in inflammation, immune modulation, bone metabolism, and cancer progression. The gene is located on chromosome 5p13.1 and is expressed in multiple tissues.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Inflammatory bowel disease (IBD) PTGER4 variants alter PGE2 signaling, affecting intestinal inflammation and mucosal integrity GWAS (NCBI, OMIM)
Rheumatoid arthritis EP4 activation promotes synovial inflammation and bone erosion Animal models and human association studies (NCBI)
Colorectal cancer PGE2/EP4 signaling drives tumor growth, angiogenesis, and immune evasion Preclinical and clinical evidence (COSMIC, NCBI)
Asthma EP4 polymorphisms linked to airway hyperresponsiveness and inflammation Genetic association studies (ClinVar, OMIM)

Expression Profile

Tissue Expression
Tissue nTPM level
Kidney 12.5 Medium
Lung 8.3 Medium
Small intestine 7.1 Medium
Colon 6.9 Medium
Spleen 5.4 Low
Whole blood 1.2 Low
Cell Line Expression
Cell Line nTPM Notes
HEK293 15.2 High expression in recombinant systems
A549 (lung) 8.7 Endogenous expression
HCT116 (colon) 6.3 Moderate expression
THP-1 (monocyte) 4.1 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G (p.Met1?) missense <0.01% Potential loss of start codon; uncertain significance (ClinVar)
c.665C>T (p.Pro222Leu) missense <0.01% Unknown effect; reported in ClinVar
c.940G>A (p.Gly314Ser) missense <0.01% Likely benign (ClinVar)
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in ClinVar or COSMIC for PTGER4.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported.

Dominant Negative (DN)

No dominant-negative mutations described.

Gene Ontology (GO)

• G-protein coupled receptor activity (GO:0004930) • prostaglandin E receptor activity (GO:0004957)
• adenylate cyclase-activating G-protein coupled receptor signaling pathway (GO:0007189) • inflammatory response (GO:0006954)
• positive regulation of cAMP-mediated signaling (GO:0030819)

Pathways

Prostanoid signaling (Reactome: R-HSA-418594)
GPCR downstream signaling (Reactome: R-HSA-388396)
PGE2-EP4 signaling in cancer (KEGG: hsa04726)

Protein Summary

PTGER4 (EP4) is a 488-amino-acid GPCR with seven transmembrane domains. It couples primarily to Gs, increasing intracellular cAMP. The receptor is activated by PGE2 and mediates diverse effects including vasodilation, pain, inflammation, and tumor promotion. It is a target for therapeutic modulation in inflammatory diseases and cancer.

Related Products

Product name Cat.No. Species Gene ID
PTGER4 Knockout HEK293 Cell Line EDJ-KQ5588 Human 5734 Details Get a Quote
PTGER4 Knockout A-549 Cell Line EDJ-KQ27605 Human 5734 Details Get a Quote
PTGER4 Knockout HCT 116 Cell Line EDJ-KQ28854 Human 5734 Details Get a Quote
PTGER4 Knockout HeLa Cell Line EDJ-KQ28855 Human 5734 Details Get a Quote
PTGER4 Knockout RT-4 Cell Line EDC07640 Human 5734 Details Get a Quote
Displaying Records 1 To 5 Of 5 Records
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