VN1R3

Chr 16

vomeronasal 1 receptor 3

Also known as: FKSG46, V1RL3, V1RL3p

The protein functions as a pheromone receptor that enables detection of chemical stimuli through G protein-coupled receptor signaling at the plasma membrane. Mutations cause disease through a dominant-negative mechanism. However, no specific neurogenetic disorders or inheritance patterns have been established for VN1R3 mutations in the pediatric population.

Summary from RefSeq, UniProt, Mechanism
0
Active trials
0
Pubs (1 yr)
2
P/LP submissions
P/LP missense
LOEUF
DN
Mechanism· predicted
Clinical SummaryVN1R3
📋
ClinVar Variants
2 unique Pathogenic / Likely Pathogenic of 2 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

DN
0.77top 25%
GOF
0.6736th %ile
LOF
0.2873th %ile

This gene has evidence for multiple mechanisms of pathogenicity (dominant-negative and gain-of-function). Both the Badonyi & Marsh prediction and the broader genomic evidence point to dominant-negative as the predominant mechanism. Different variants in this gene may act through different mechanisms — interpret in context of the specific variant.

DNprediction above median
GOFprediction above median

Note: In-silico variant effect predictors (SIFT, PolyPhen, REVEL, CADD) may underestimate pathogenicity of missense variants in genes with GOF or DN mechanisms. Consider functional evidence and clinical context.

Predictions from Badonyi M, Marsh JA. PLoS ONE. 2024;19(8):e0307312.

ClinVar Variant Classifications

2 submitted variants in ClinVar

Classification Summary

Pathogenic2
2
Pathogenic

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
2
Likely Pathogenic
0
VUS
0
Likely Benign
0
Benign
0
Total2

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

VN1R3 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found