NPY1R Gene - Neuropeptide Y Receptor Y1

Complete genetic and functional information for NPY1R

Gene Information Card

Symbol NPY1R
Full Name neuropeptide Y receptor Y1
Gene Type gene with protein product
Chromosomal Location 4q32.2
NCBI Gene ID 4886 ncbi.nlm.nih.gov/gene/4886
Ensembl ID ENSG00000164128
UniProt ID P25929
OMIM ID 162641
HGNC ID HGNC:7956
Aliases NPYR

Description

NPY1R encodes the neuropeptide Y receptor Y1, a G protein-coupled receptor for neuropeptide Y (NPY), peptide YY (PYY), and pancreatic polypeptide (PP). It is involved in regulation of food intake, energy homeostasis, anxiety, and vasoconstriction. The receptor is expressed in various tissues including brain, adipose tissue, and vasculature, and has been implicated in obesity, cardiovascular diseases, and certain cancers.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Obesity NPY1R signaling in hypothalamus regulates appetite; altered expression or function may contribute to obesity. PMID: 10673429
Anxiety NPY1R activation in amygdala produces anxiolytic effects; dysregulation linked to anxiety disorders. PMID: 15159515
Cardiovascular diseases NPY1R mediates vasoconstriction and cardiac hypertrophy; implicated in hypertension and heart failure. PMID: 12135968
Cancer NPY1R expression in various tumors (e.g., breast, prostate) may promote proliferation and metastasis. PMID: 22198343

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 8.2 Medium
Adipose tissue 5.1 Low
Heart 3.4 Low
Vasculature 6.7 Medium
Gastrointestinal tract 4.5 Low
Cell Line Expression
Cell Line nTPM Notes
SH-SY5Y 12.3 Neuroblastoma cell line; high expression
MCF-7 7.8 Breast cancer cell line; moderate expression
HepG2 2.1 Hepatocellular carcinoma; low expression
A549 1.5 Lung carcinoma; very low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
rs1042044 SNP 0.32 Missense variant (Leu7Ile) in signal peptide; associated with altered receptor expression and obesity risk.
rs7687423 SNP 0.15 Intronic variant; may affect splicing and expression.
c.1058C>T SNV 0.01 Nonsense variant (p.Arg353Ter); predicted to cause loss of function.
c.112G>A SNV 0.02 Missense variant (p.Ala38Thr); affects ligand binding.
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations leading to truncated or absent receptor protein.

Gain of Function (GOF)

Missense mutations that increase receptor activity or constitutive signaling.

Dominant Negative (DN)

Mutations that produce a receptor that interferes with wild-type function, e.g., by forming inactive dimers.

Gene Ontology (GO)

• G protein-coupled receptor activity • neuropeptide Y receptor activity
• peptide YY receptor activity • pancreatic polypeptide receptor activity
• plasma membrane • integral component of plasma membrane
• signal transduction • G protein-coupled receptor signaling pathway
• feeding behavior • vasoconstriction

Pathways

Neuropeptide Y signaling pathway
GPCR downstream signaling
Regulation of appetite
Cardiac hypertrophy signaling

Protein Summary

NPY1R is a 384-amino acid G protein-coupled receptor with seven transmembrane domains. It couples to Gi/Go proteins, inhibiting adenylate cyclase and modulating intracellular calcium. The receptor is involved in diverse physiological processes including appetite regulation, anxiety, and blood pressure control. It is a potential therapeutic target for obesity, anxiety, and cardiovascular disorders.

Related Products

Product name Cat.No. Species Gene ID
NPY1R Knockout HEK293 Cell Line EDJ-KQ1789 Human 4886 Details Get a Quote
NPY1R Knockout HeLa Cell Line EDJ-KQ54019 Human 4886 Details Get a Quote
NPY1R Knockout A-549 Cell Line EDJ-KQ62509 Human 4886 Details Get a Quote
NPY1R Knockout HCT 116 Cell Line EDJ-KQ70980 Human 4886 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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