GALR1: Galanin Receptor 1

A G-protein coupled receptor for galanin, involved in neuromodulation, pain, and cancer.

Gene Information Card

Symbol GALR1
Full Name galanin receptor 1
Gene Type protein-coding
Chromosomal Location 18q23
NCBI Gene ID 2587 ncbi.nlm.nih.gov/gene/2587
Ensembl ID ENSG00000166573
UniProt ID P47211
OMIM ID 600377
HGNC ID 4132
Aliases GALNR1, GALR-1

Description

GALR1 encodes a G-protein coupled receptor for the neuropeptide galanin. The receptor is predominantly expressed in the central and peripheral nervous systems and mediates galanin's effects on pain modulation, feeding behavior, memory, and neuroendocrine function. It signals through Gi/Go proteins to inhibit adenylyl cyclase and modulate ion channels. Altered expression and mutations have been implicated in head and neck squamous cell carcinoma, colorectal cancer, and neurological disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Head and Neck Squamous Cell Carcinoma Hypermethylation of GALR1 promoter leads to transcriptional silencing, reducing tumor suppression. ClinVar, COSMIC
Colorectal Cancer Loss of GALR1 expression via promoter methylation correlates with poor prognosis. NCBI Gene, PubMed
Pain Disorders GALR1 activation modulates nociception; polymorphisms may alter pain sensitivity. OMIM, PubMed

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 2.3 Low
Spinal Cord 1.8 Low
Pituitary 4.1 Medium
Small Intestine 0.9 Not detected
Colon 0.5 Not detected
Cell Line Expression
Cell Line nTPM Notes
SH-SY5Y (neuroblastoma) 1.2 Low expression
U-87 MG (glioblastoma) 0.8 Not detected
HeLa (cervical carcinoma) 0.3 Not detected
MCF7 (breast cancer) 0.6 Not detected
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G (p.Met1?) missense <0.01% Likely loss of start codon; predicted loss of function
c.200C>T (p.Thr67Ile) missense <0.01% Unknown significance; rare population variant
c.1034G>A (p.Arg345Gln) missense <0.01% Located in C-terminal tail; functional impact uncertain
Mutation functional classification

Loss of Function (LOF)

Promoter hypermethylation leading to transcriptional silencing is the primary loss-of-function mechanism in cancer.

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 • galanin receptor activity
• G protein-coupled receptor signaling pathway • adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway
• neuropeptide signaling pathway • plasma membrane
• integral component of plasma membrane

Pathways

G alpha (i) signalling events
Neuropeptide GPCR signaling
Class A/1 (Rhodopsin-like) GPCRs

Protein Summary

Galanin receptor 1 (GALR1) is a 349-amino acid integral membrane protein with seven transmembrane domains, characteristic of G-protein coupled receptors. It binds the neuropeptide galanin with high affinity and couples primarily to pertussis toxin-sensitive Gi/Go proteins, leading to inhibition of adenylyl cyclase, reduction of cAMP levels, and modulation of potassium and calcium channels. The receptor is involved in regulating pain transmission, feeding, memory, and neuroendocrine secretion. In cancer, epigenetic silencing of GALR1 is associated with tumor progression.

Related Products

Product name Cat.No. Species Gene ID
GALR1 Knockout HEK293 Cell Line EDJ-KQ1116 Human 2587 Details Get a Quote
GALR1 Knockout HeLa Cell Line EDJ-KQ53302 Human 2587 Details Get a Quote
GALR1 Knockout A-549 Cell Line EDJ-KQ61785 Human 2587 Details Get a Quote
GALR1 Knockout HCT 116 Cell Line EDJ-KQ70267 Human 2587 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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