NPBWR1: Neuropeptides B/W Receptor 1

G protein-coupled receptor for neuropeptide B and W, involved in energy homeostasis and neuroendocrine signaling.

Gene Information Card

Symbol NPBWR1
Full Name Neuropeptides B/W Receptor 1
Gene Type protein-coding
Chromosomal Location 8q11.23
NCBI Gene ID 2831 ncbi.nlm.nih.gov/gene/2831
Ensembl ID ENSG00000104419
UniProt ID P48145
OMIM ID 600730
HGNC ID 4529
Aliases GPR7, NPBW1

Description

NPBWR1 encodes a G protein-coupled receptor (GPCR) that binds neuropeptide B (NPB) and neuropeptide W (NPW). It is primarily expressed in the central nervous system and plays a role in energy homeostasis, feeding behavior, pain modulation, and neuroendocrine regulation. The receptor signals through G_i/o proteins, inhibiting adenylate cyclase and modulating intracellular calcium levels.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Obesity Altered NPBWR1 signaling may disrupt energy balance and appetite regulation, contributing to obesity. OMIM #600730; association studies in human cohorts.
Neuroendocrine tumors Aberrant expression of NPBWR1 has been observed in certain pituitary and adrenal tumors, suggesting a role in tumorigenesis. COSMIC; limited case reports.

Expression Profile

Tissue Expression
Tissue nTPM level
Brain (cerebral cortex) 2.3 Low
Hypothalamus 4.1 Medium
Pituitary gland 3.8 Medium
Adrenal gland 1.5 Low
Testis 0.9 Not detected
Cell Line Expression
Cell Line nTPM Notes
SH-SY5Y (neuroblastoma) 1.8 Low expression
HEK293 (embryonic kidney) 0.2 Not detected
HeLa (cervical carcinoma) 0.1 Not detected
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.200C>T (p.Pro67Leu) Missense <0.01% Unknown functional impact; rare population variant.
c.487G>A (p.Val163Met) Missense <0.01% Predicted benign; no known disease association.
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in NPBWR1.

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 • neuropeptide binding
• neuropeptide Y receptor activity • plasma membrane
• signal transduction • G protein-coupled receptor signaling pathway
• feeding behavior • energy homeostasis

Pathways

• Neuropeptide signaling (Reactome: R-HSA-375276)
• GPCR downstream signaling (Reactome: R-HSA-388396)

Protein Summary

NPBWR1 is a 7-transmembrane GPCR of the rhodopsin family. It is activated by endogenous neuropeptides B and W, leading to inhibition of cAMP production via G_i/o proteins. The receptor is highly expressed in the hypothalamus and pituitary, where it modulates appetite, stress response, and pain perception. Structural studies indicate conserved motifs for ligand binding and G protein coupling.

Related Products

Product name Cat.No. Species Gene ID
NPBWR1 Knockout HEK293 Cell Line EDJ-KQ4757 Human 2831 Details Get a Quote
NPBWR1 Knockout HeLa Cell Line EDJ-KQ53386 Human 2831 Details Get a Quote
NPBWR1 Knockout A-549 Cell Line EDJ-KQ61864 Human 2831 Details Get a Quote
NPBWR1 Knockout HCT 116 Cell Line EDJ-KQ70346 Human 2831 Details Get a Quote
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