PRLHR

Prolactin Releasing Hormone Receptor

Gene Information Card

Symbol PRLHR
Full Name Prolactin Releasing Hormone Receptor
Gene Type protein-coding
Chromosomal Location 10q11.22
NCBI Gene ID 2834 ncbi.nlm.nih.gov/gene/2834
Ensembl ID ENSG00000119973
UniProt ID P49683
OMIM ID 600895
HGNC ID 9363
Aliases GPR10, GrPR, hGR3

Description

PRLHR encodes the prolactin-releasing hormone receptor, a G-protein coupled receptor (GPCR) that binds prolactin-releasing peptide (PrRP). It is primarily expressed in the pituitary, brain, and peripheral tissues, and plays a role in neuroendocrine regulation, including prolactin secretion, stress response, energy homeostasis, and pain modulation.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Obesity PRLHR signaling modulates energy balance and appetite; loss-of-function variants are associated with increased body weight in animal models. NCBI Gene, OMIM
Prolactinoma PRLHR expression is altered in pituitary adenomas, potentially affecting prolactin secretion. NCBI Gene, COSMIC
Breast Cancer PRLHR is overexpressed in some breast cancer cell lines and may influence tumor growth via GPCR signaling. COSMIC, UniProt

Expression Profile

Tissue Expression
Tissue nTPM level
Pituitary 12.5 Medium
Hypothalamus 8.3 Low
Adrenal Gland 6.1 Low
Placenta 4.7 Low
Breast 3.2 Low
Cell Line Expression
Cell Line nTPM Notes
MCF7 (breast cancer) 5.1 Moderate expression
HEK293 (embryonic kidney) 2.3 Low expression
SH-SY5Y (neuroblastoma) 4.8 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.200G>A (p.Arg67Gln) Missense <0.01% Unknown functional effect
c.487C>T (p.Arg163Trp) Missense <0.01% Potential loss of function
c.1A>G (p.Met1Val) Start loss <0.01% Likely loss of function
Mutation functional classification

Loss of Function (LOF)

Missense and start-loss variants (e.g., p.Met1Val) likely impair receptor expression or signaling.

Gain of Function (GOF)

No gain-of-function mutations reported in PRLHR.

Dominant Negative (DN)

No dominant-negative mutations reported.

Gene Ontology (GO)

• G protein-coupled receptor activity • neuropeptide receptor activity
• prolactin-releasing peptide receptor activity • plasma membrane
• signal transduction • adenylate cyclase-activating G protein-coupled receptor signaling pathway

Pathways

GPCR downstream signaling
Neuropeptide signaling pathway
Prolactin regulation

Protein Summary

PRLHR is a 377-amino acid GPCR with seven transmembrane domains. It is activated by PrRP, leading to intracellular calcium mobilization and inhibition of cAMP production. The receptor is involved in neuroendocrine functions, including prolactin release, stress response, and energy homeostasis.

Related Products

Product name Cat.No. Species Gene ID
PRLHR Knockout HEK293 Cell Line EDJ-KQ4777 Human 2834 Details Get a Quote
PRLHR Knockout HeLa Cell Line EDJ-KQ53389 Human 2834 Details Get a Quote
PRLHR Knockout A-549 Cell Line EDJ-KQ61867 Human 2834 Details Get a Quote
PRLHR Knockout HCT 116 Cell Line EDJ-KQ70349 Human 2834 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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