VN1R4

gene
On this page

Also known as V1RL4

Summary

VN1R4 (vomeronasal 1 receptor 4, HGNC:19871) is a protein-coding gene on chromosome 19q13.42, encoding Vomeronasal type-1 receptor 4 (Q7Z5H5). Putative pheromone receptor.

Predicted to enable pheromone receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway; response to pheromone; and sensory perception of chemical stimulus. Predicted to be located in plasma membrane.

Source: NCBI Gene 317703 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 51 total
  • MANE Select transcript: NM_173857

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:19871
Approved symbolVN1R4
Namevomeronasal 1 receptor 4
Location19q13.42
Locus typegene with protein product
StatusApproved
AliasesV1RL4
Ensembl geneENSG00000228567
Ensembl biotypeprotein_coding
Entrez317703

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000311170

RefSeq mRNA: 1 — MANE Select: NM_173857 NM_173857

CCDS: CCDS33099

Canonical transcript exons

ENST00000311170 — 1 exons

ExonStartEnd
ENSE000014194915326667653267723

Expression profiles

Bgee: expression breadth tissue_specific, 3 present calls, max score 92.86.

Top tissues by expression

129 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047392.86gold quality
stromal cell of endometriumCL:000225539.95gold quality
colonic epitheliumUBERON:000039737.20gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
bone marrowUBERON:000237131.74gold quality
muscle tissueUBERON:000238531.06gold quality
sural nerveUBERON:001548830.93gold quality
right uterine tubeUBERON:000130230.49gold quality
prefrontal cortexUBERON:000045129.04gold quality
monocyteCL:000057628.58gold quality
leukocyteCL:000073828.49gold quality
duodenumUBERON:000211428.14gold quality
liverUBERON:000210728.04gold quality
testisUBERON:000047327.87gold quality
lymph nodeUBERON:000002927.57gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.55gold quality
vermiform appendixUBERON:000115426.42gold quality
bloodUBERON:000017826.15gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
urinary bladderUBERON:000125525.72gold quality
calcaneal tendonUBERON:000370124.97gold quality
primary visual cortexUBERON:000243624.61gold quality
superior frontal gyrusUBERON:000266124.08gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no1.31

Regulation

Is transcription factor: no

Cross-species orthologs

13 orthologs

OrganismSymbolGene ID
mus_musculusVmn1r233ENSMUSG00000045575
mus_musculusVmn1r235ENSMUSG00000050102
mus_musculusVmn1r236ENSMUSG00000054142
mus_musculusVmn1r234ENSMUSG00000057203
mus_musculusVmn1r237ENSMUSG00000058030
rattus_norvegicusVom1r22ENSRNOG00000025949
rattus_norvegicusVom1r17ENSRNOG00000064083
rattus_norvegicusVom1r16ENSRNOG00000067452
rattus_norvegicusVom1r-ps20ENSRNOG00000068980
rattus_norvegicusVom1r23ENSRNOG00000078217
rattus_norvegicusVom1r21ENSRNOG00000078543
rattus_norvegicusVom1r16ENSRNOG00000084531
rattus_norvegicusVmn1r235ENSRNOG00000087999

Paralogs (3): VN1R1 (ENSG00000178201), VN1R2 (ENSG00000196131), VN1R5 (ENSG00000197617)

Protein

Protein identifiers

Vomeronasal type-1 receptor 4Q7Z5H5 (reviewed: Q7Z5H5)

Alternative names: G-protein coupled receptor GPCR27, V1r-like receptor 4

All UniProt accessions (1): Q7Z5H5

UniProt curated annotations — full annotation on UniProt →

Function. Putative pheromone receptor.

Subcellular location. Cell membrane.

Polymorphism. Various VN1R4 alleles are known. The sequence shown is that of allele VN1R4*2.

Miscellaneous. The chimpanzee and gorilla orthologous proteins do not exist, their genes are pseudogenes.

Similarity. Belongs to the G-protein coupled receptor 1 family.

RefSeq proteins (1): NP_776256* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR004072Vmron_rcpt_1Family
IPR017452GPCR_Rhodpsn_7TMDomain

Pfam: PF03402

UniProt features (21 total): topological domain 8, transmembrane region 7, sequence variant 3, glycosylation site 2, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q7Z5H5-F177.440.20

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Glycosylation sites (2): 154, 157

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 20 (showing top): GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, GOBP_SENSORY_PERCEPTION, GOMF_TRANSMEMBRANE_SIGNALING_RECEPTOR_ACTIVITY, GOMF_ODORANT_BINDING, GOMF_G_PROTEIN_COUPLED_RECEPTOR_ACTIVITY, GOBP_G_PROTEIN_COUPLED_RECEPTOR_SIGNALING_PATHWAY, GOBP_RESPONSE_TO_PHEROMONE, RAO_BOUND_BY_SALL4_ISOFORM_A, RAO_BOUND_BY_SALL4_ISOFORM_B, GSE13485_CTRL_VS_DAY21_YF17D_VACCINE_PBMC_DN, GSE13485_DAY3_VS_DAY21_YF17D_VACCINE_PBMC_DN, GSE2706_LPS_VS_R848_AND_LPS_2H_STIM_DC_UP, GOMF_PHEROMONE_BINDING, GOMF_MOLECULAR_TRANSDUCER_ACTIVITY, chr19q13

GO Biological Process (4): sensory perception of chemical stimulus (GO:0007606), response to pheromone (GO:0019236), signal transduction (GO:0007165), G protein-coupled receptor signaling pathway (GO:0007186)

GO Molecular Function (3): pheromone binding (GO:0005550), pheromone receptor activity (GO:0016503), G protein-coupled receptor activity (GO:0004930)

GO Cellular Component (2): plasma membrane (GO:0005886), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
G protein-coupled receptor activity2
sensory perception1
response to chemical1
cell communication1
cellular process1
signaling1
regulation of cellular process1
cellular response to stimulus1
signal transduction1
odorant binding1
pheromone binding1
transmembrane signaling receptor activity1
G protein-coupled receptor signaling pathway1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

212 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
VN1R4OR52E8Q6IFG1570
VN1R4OR51A4Q8NGJ6528
VN1R4OR10A2Q9H208518
VN1R4OR4F4Q96R69513
VN1R4OR52K2Q8NGK3507
VN1R4OR10G8Q8NGN5507
VN1R4OR2T1O43869506
VN1R4OR52K1Q8NGK4480
VN1R4OR52M1Q8NGK5480
VN1R4OR2T33Q8NG76479
VN1R4OR52B6Q8NGF0479
VN1R4OR6F1Q8NGZ6479
VN1R4OR4N4Q8N0Y3475
VN1R4OR51A7Q8NH64475
VN1R4ZNF845Q96IR2449

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: P59530, P59541, P59542, P59544, Q5J3F6, Q5J3L6, Q5J3M4, Q5Y4Y9, Q62850, Q645T2, Q645T3, Q645T4, Q645T7, Q645V2, Q645V4, Q645V7, Q645V8, Q645Z2, Q645Z6, Q645Z9, Q646A2, Q646B7, Q646C1, Q646C4, Q646D6, Q646D9, Q646E2, Q646F4, Q646F6, Q646F7, Q646F8, Q646F9, Q646G0, Q67ES0, Q67ET4, Q7M710, Q7M713, Q7M721, Q7TQA4, Q7YRP2

Diamond homologs: A0A0R4IM31, Q7YRP1, Q7Z5H4, Q7Z5H5, Q8WN92, Q9GZP7, Q5J3E5, Q5J3F6, Q5J3G9, Q5J3K5, Q5J3K9, Q5J3L4, Q5J3L6, Q5J3L7, Q5J3M3, Q5J3M4, Q5J3M9, Q5J3N1, Q62850, Q7YRP2, Q8NFZ6, Q8R2E6, Q8TDU5, Q8VBS7, Q8VIC6, Q8VIC7, Q8VIC9, Q9BXE9, Q9EP51, Q9EP79, Q9EP93, Q9EPB8, Q9EQ44, Q9EQ45, Q9EQ46, Q9EQ47, Q9EQ48, Q9EQ51, Q9EQ52, Q9WUF1

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

51 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance48
Likely benign2
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

205 predictions. Top by Δscore:

VariantEffectΔscore
19:53267222:A:Cacceptor_gain0.9300
19:53267401:CT:Cacceptor_gain0.8700
19:53267360:ACTC:Aacceptor_gain0.8100
19:53267263:A:Tacceptor_gain0.8000
19:53267650:CATA:Cdonor_loss0.7800
19:53267651:ATACC:Adonor_loss0.7800
19:53267652:TA:Tdonor_loss0.7800
19:53267653:ACCGG:Adonor_loss0.7800
19:53267358:ACACT:Aacceptor_gain0.7700
19:53267359:CACTC:Cacceptor_gain0.7700
19:53267361:CTC:Cacceptor_gain0.7700
19:53267362:T:Aacceptor_gain0.7700
19:53267648:CACAT:Cdonor_loss0.7500
19:53267649:ACATA:Adonor_loss0.7500
19:53267403:C:CCacceptor_gain0.7100
19:53267653:A:ACdonor_gain0.7100
19:53267654:C:CCdonor_gain0.7100
19:53267226:A:Cacceptor_gain0.6800
19:53267398:CCACT:Cacceptor_gain0.6700
19:53267399:CACTC:Cacceptor_gain0.6700
19:53267612:TCC:Tdonor_gain0.6400
19:53267613:CCC:Cdonor_gain0.6400
19:53267222:A:ACacceptor_gain0.6100
19:53267265:C:CTacceptor_gain0.6100
19:53267399:CACT:Cacceptor_gain0.6000
19:53267655:C:Adonor_loss0.5900
19:53267262:C:CTacceptor_gain0.5800
19:53267425:T:TAacceptor_gain0.5700
19:53267090:C:Tacceptor_gain0.5500
19:53267267:C:CTacceptor_gain0.5500

AlphaMissense

1977 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:53266835:G:CF277L0.894
19:53266835:G:TF277L0.894
19:53266837:A:GF277L0.894
19:53266940:A:CF242L0.889
19:53266940:A:TF242L0.889
19:53266942:A:GF242L0.889
19:53267354:G:CF104L0.803
19:53267354:G:TF104L0.803
19:53267356:A:GF104L0.803
19:53266817:A:CF283L0.714
19:53266817:A:TF283L0.714
19:53266819:A:GF283L0.714
19:53267231:A:CF145L0.709
19:53267231:A:TF145L0.709
19:53267233:A:GF145L0.709
19:53266946:G:CS240R0.668
19:53266946:G:TS240R0.668
19:53266948:T:GS240R0.668
19:53267414:G:CF84L0.661
19:53267414:G:TF84L0.661
19:53267416:A:GF84L0.661
19:53267444:A:CF74L0.634
19:53267444:A:TF74L0.634
19:53267446:A:GF74L0.634
19:53267459:A:CF69L0.612
19:53267459:A:TF69L0.612
19:53267461:A:GF69L0.612
19:53267069:G:CS199R0.606
19:53267069:G:TS199R0.606
19:53267071:T:GS199R0.606

dbSNP variants (sampled 300 via entrez): RS1000488478 (19:53268230 A>G), RS1000860261 (19:53269283 G>A), RS1001227291 (19:53269121 T>A,C), RS1002848699 (19:53266554 A>G), RS1002945503 (19:53266727 T>A,C,G), RS1003326821 (19:53268022 C>T), RS1003620369 (19:53267829 G>A), RS1004888873 (19:53268755 A>G), RS1005636211 (19:53269574 G>T), RS1007080343 (19:53266179 T>A), RS1007114894 (19:53266463 T>C), RS1007449988 (19:53267746 T>TATA), RS1009187120 (19:53268705 A>G,T), RS1009406493 (19:53269375 G>A,T), RS1009522463 (19:53269531 C>A,T)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

1 associations (top):

StudyTraitp-value
GCST009391_771Metabolite levels5.000000e-06

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0010393sphingomyelin 18:0 measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

7 total (human), top 7 by PubMed support.

ChemicalActions (top 5)PubMed papers
arsenitedecreases methylation1
1-hydroxypyrenedecreases expression1
CGP 52608affects binding, increases reaction1
Air Pollutants, Occupationaldecreases expression1
Benzo(a)pyreneincreases expression1
Phthalic Acidsincreases methylation1
Aflatoxin B1increases methylation1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.