PTGFR (Prostaglandin F Receptor)

FP receptor, a G-protein coupled receptor for prostaglandin F2α, involved in smooth muscle contraction, parturition, and glaucoma pathogenesis.

Gene Information Card

Symbol PTGFR
Full Name Prostaglandin F Receptor
Gene Type protein-coding
Chromosomal Location 1p31.1
NCBI Gene ID 5737 ncbi.nlm.nih.gov/gene/5737
Ensembl ID ENSG00000122420
UniProt ID P43088
OMIM ID 600563
HGNC ID 9599
Aliases FP, FP receptor, PTGFR1

Description

The PTGFR gene encodes the prostaglandin F receptor (FP), a member of the G-protein coupled receptor family. This receptor binds prostaglandin F2α (PGF2α) and mediates its physiological effects, including smooth muscle contraction, luteolysis, and induction of labor. It is also a therapeutic target in glaucoma, where FP receptor agonists reduce intraocular pressure.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Glaucoma (primary open-angle) FP receptor activation lowers intraocular pressure; mutations may alter receptor function ClinVar, OMIM
Preterm labor PGF2α signaling via FP receptor induces uterine contractions; dysregulation linked to preterm birth OMIM, PubMed
Corpus luteum regression (luteolysis) FP receptor mediates luteolysis; aberrant signaling may affect fertility OMIM, PubMed

Expression Profile

Tissue Expression
Tissue nTPM level
Uterus 12.3 Medium
Eye (ciliary body) 8.7 Medium
Ovary 6.5 Low
Lung 4.2 Low
Kidney 3.1 Low
Cell Line Expression
Cell Line nTPM Notes
HEK293 15.2 Overexpressed in recombinant systems
HeLa 2.1 Endogenous expression
A549 1.8 Low endogenous expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.125G>A (p.Arg42His) missense <0.01% Unknown; predicted benign
c.682C>T (p.Arg228Cys) missense <0.01% Unknown; predicted possibly damaging
c.1037_1038insA frameshift <0.01% Loss of function
Mutation functional classification

Loss of Function (LOF)

Frameshift insertions or nonsense variants that truncate the receptor, impairing PGF2α binding and signaling.

Gain of Function (GOF)

Not well documented; activating mutations are rare and not clinically characterized.

Dominant Negative (DN)

No dominant-negative variants reported in PTGFR.

Gene Ontology (GO)

• G-protein coupled receptor activity • prostaglandin F receptor activity
• plasma membrane • signal transduction
• smooth muscle contraction • luteolysis
• positive regulation of cytosolic calcium ion concentration

Pathways

Prostanoid signaling pathway
GPCR downstream signaling
Smooth muscle contraction

Protein Summary

The PTGFR protein (FP receptor) is a 359-amino acid G-protein coupled receptor with seven transmembrane domains. Upon binding PGF2α, it activates Gq/11 proteins, leading to phospholipase C activation, inositol trisphosphate production, and intracellular calcium mobilization. This triggers smooth muscle contraction, luteolysis, and regulation of intraocular pressure.

Related Products

Product name Cat.No. Species Gene ID
PTGFR Knockout HEK293 Cell Line EDJ-KQ1600 Human 5737 Details Get a Quote
PTGFRN Knockout HEK293 Cell Line EDJ-KQ3249 Human 5738 Details Get a Quote
PTGFRN Knockout A-549 Cell Line EDJ-KQ23391 Human 5738 Details Get a Quote
PTGFRN Knockout HCT 116 Cell Line EDJ-KQ24783 Human 5738 Details Get a Quote
PTGFRN Knockout HeLa Cell Line EDJ-KQ24784 Human 5738 Details Get a Quote
PTGFR Knockout HeLa Cell Line EDJ-KQ54259 Human 5737 Details Get a Quote
PTGFR Knockout A-549 Cell Line EDJ-KQ62750 Human 5737 Details Get a Quote
PTGFR Knockout HCT 116 Cell Line EDJ-KQ71218 Human 5737 Details Get a Quote
Displaying Records 1 To 8 Of 8 Records
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