PRLH (Prolactin Releasing Hormone)

Gene encoding the prolactin-releasing peptide (PrRP), a neuropeptide involved in prolactin secretion, stress response, and energy homeostasis.

Gene Information Card

Symbol PRLH
Full Name Prolactin Releasing Hormone
Gene Type protein-coding
Chromosomal Location 2q37.3
NCBI Gene ID 51095 ncbi.nlm.nih.gov/gene/51095
Ensembl ID ENSG00000163041
UniProt ID P81277
OMIM ID 602663
HGNC ID 17952
Aliases PrRP, PRH, prolactin-releasing peptide

Description

The PRLH gene encodes prolactin-releasing peptide (PrRP), a neuropeptide primarily expressed in the hypothalamus. PrRP binds to the GPR10 receptor (also known as PrRPR) to stimulate prolactin secretion from the anterior pituitary. Beyond prolactin regulation, PrRP is involved in stress response, energy balance, and feeding behavior. The gene is located on chromosome 2q37.3 and consists of two exons.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Obesity PrRP signaling modulates energy homeostasis; loss-of-function variants may contribute to hyperphagia and weight gain. PMID: 17974916; OMIM #602663
Stress-related disorders PrRP is upregulated in response to stress and may influence anxiety and depression through hypothalamic-pituitary-adrenal axis modulation. PMID: 17974916; NCBI Gene
Prolactinoma Altered PrRP expression may contribute to abnormal prolactin secretion in pituitary tumors. PMID: 17974916; COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Hypothalamus 12.5 Medium
Pituitary 8.2 Low
Adrenal gland 6.1 Low
Placenta 4.3 Low
Testis 3.7 Low
Cell Line Expression
Cell Line nTPM Notes
SH-SY5Y (neuroblastoma) 5.1 Neuronal model
HeLa (cervical carcinoma) 2.3 Low expression
HepG2 (hepatocellular carcinoma) 1.8 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; predicted loss of function
c.85C>T (p.Arg29Trp) missense <0.01% Unknown significance; not reported in ClinVar
Mutation functional classification

Loss of Function (LOF)

Loss-of-function mutations in PRLH may impair PrRP signaling, potentially leading to altered prolactin secretion and metabolic dysregulation.

Gain of Function (GOF)

No gain-of-function mutations have been reported for PRLH.

Dominant Negative (DN)

No dominant-negative mutations have been described for PRLH.

Pathways

Prolactin signaling pathway (KEGG hsa04917)
Neuroactive ligand-receptor interaction (KEGG hsa04080)

Protein Summary

The PRLH gene encodes a 20-amino-acid mature peptide (prolactin-releasing peptide, PrRP) after cleavage from a 98-amino-acid precursor. PrRP is a neuropeptide that binds to the GPR10 receptor to stimulate prolactin release. It also plays roles in stress response, energy balance, and feeding regulation. The protein is primarily expressed in the hypothalamus and is secreted into the pituitary portal circulation.

Related Products

Product name Cat.No. Species Gene ID
PRLHR Knockout HEK293 Cell Line EDJ-KQ4777 Human 2834 Details Get a Quote
PRLH Knockout HEK293 Cell Line EDJ-KQ10889 Human 51052 Details Get a Quote
PRLHR Knockout HeLa Cell Line EDJ-KQ53389 Human 2834 Details Get a Quote
PRLH Knockout HeLa Cell Line EDJ-KQ56220 Human 51052 Details Get a Quote
PRLHR Knockout A-549 Cell Line EDJ-KQ61867 Human 2834 Details Get a Quote
PRLH Knockout A-549 Cell Line EDJ-KQ64711 Human 51052 Details Get a Quote
PRLHR Knockout HCT 116 Cell Line EDJ-KQ70349 Human 2834 Details Get a Quote
PRLH Knockout HCT 116 Cell Line EDJ-KQ73156 Human 51052 Details Get a Quote
Displaying Records 1 To 8 Of 8 Records
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