OR4C3

gene
On this page

Summary

OR4C3 (olfactory receptor family 4 subfamily C member 3, HGNC:14697) is a protein-coding gene on chromosome 11p11.2, encoding Olfactory receptor 4C3 (Q8NH37). Odorant receptor.

Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome.

Source: NCBI Gene 256144 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 2 total
  • MANE Select transcript: NM_001004702

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:14697
Approved symbolOR4C3
Nameolfactory receptor family 4 subfamily C member 3
Location11p11.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000176547
Ensembl biotypeprotein_coding
Entrez256144

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000319856

RefSeq mRNA: 1 — MANE Select: NM_001004702 NM_001004702

CCDS: CCDS31489

Canonical transcript exons

ENST00000319856 — 1 exons

ExonStartEnd
ENSE000012602954832492048325955

Expression profiles

Bgee: expression breadth tissue_specific, 1 present calls, max score 37.20.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
colonic epitheliumUBERON:000039737.20gold quality
sural nerveUBERON:001548836.74gold 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
hindlimb stylopod muscleUBERON:000425232.15gold quality
bone marrowUBERON:000237131.74gold quality
muscle tissueUBERON:000238531.06gold quality
monocyteCL:000057631.03silver quality
leukocyteCL:000073830.72silver quality
stromal cell of endometriumCL:000225529.87gold quality
prefrontal cortexUBERON:000045129.04gold quality
liverUBERON:000210728.58gold quality
duodenumUBERON:000211428.14gold quality
lymph nodeUBERON:000002927.57gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.55gold quality
vermiform appendixUBERON:000115426.42gold quality
cortex of kidneyUBERON:000122526.42silver quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
muscle of legUBERON:000138325.06gold quality
primary visual cortexUBERON:000243624.61gold quality
superior frontal gyrusUBERON:000266124.08gold quality
pancreasUBERON:000126424.01gold quality
frontal cortexUBERON:000187023.91gold quality
gastrocnemiusUBERON:000138823.88gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.47

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): HNF4A

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusOr4c3ENSMUSG00000075069
rattus_norvegicusOr4c3ENSRNOG00000081832

Paralogs (130): OR1I1 (ENSG00000094661), OR12D3 (ENSG00000112462), OR7A10 (ENSG00000127515), OR7C2 (ENSG00000127529), OR7C1 (ENSG00000127530), OR1E2 (ENSG00000127780), OR1J1 (ENSG00000136834), OR1L4 (ENSG00000136939), OR4D1 (ENSG00000141194), OR4K1 (ENSG00000155249), OR3A3 (ENSG00000159961), OR7G1 (ENSG00000161807), OR1Q1 (ENSG00000165202), OR1K1 (ENSG00000165204), OR4K2 (ENSG00000165762), OR4D6 (ENSG00000166884), OR1F1 (ENSG00000168124), OR4K14 (ENSG00000169484), OR4K15 (ENSG00000169488), OR7G3 (ENSG00000170920), OR7G2 (ENSG00000170923), OR1M1 (ENSG00000170929), OR4D5 (ENSG00000171014), OR1L6 (ENSG00000171459), OR1L3 (ENSG00000171481), OR1L8 (ENSG00000171496), OR1N2 (ENSG00000171501), OR1N1 (ENSG00000171505), OR2AT4 (ENSG00000171561), OR1A1 (ENSG00000172146), OR1A2 (ENSG00000172150), OR4C11 (ENSG00000172188), OR4X2 (ENSG00000172208), OR4D9 (ENSG00000172742), OR10K1 (ENSG00000173285), OR1L1 (ENSG00000173679), OR7D4 (ENSG00000174667), OR4S2 (ENSG00000174982), OR4B1 (ENSG00000175619), OR4D11 (ENSG00000176200)

Protein

Protein identifiers

Olfactory receptor 4C3Q8NH37 (reviewed: Q8NH37)

Alternative names: Olfactory receptor OR11-98

All UniProt accessions (2): A0A126GW65, Q8NH37

UniProt curated annotations — full annotation on UniProt →

Function. Odorant receptor.

Subcellular location. Cell membrane.

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

RefSeq proteins (1): NP_001004702* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain
IPR050427Olfactory_ReceptorsFamily

Pfam: PF13853

UniProt features (18 total): topological domain 8, transmembrane region 7, chain 1, glycosylation site 1, disulfide bond 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8NH37-F189.610.64

Functional residue map

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

Disulfide bonds (1): 95–187

Glycosylation sites (1): 6

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-9752946Expression and translocation of olfactory receptors

MSigDB gene sets: 25 (showing top): GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, KEGG_OLFACTORY_TRANSDUCTION, GOBP_DETECTION_OF_STIMULUS, GOBP_SENSORY_PERCEPTION, GOMF_OLFACTORY_RECEPTOR_ACTIVITY, GOMF_TRANSMEMBRANE_SIGNALING_RECEPTOR_ACTIVITY, GOMF_G_PROTEIN_COUPLED_RECEPTOR_ACTIVITY, GOBP_SENSORY_PERCEPTION_OF_SMELL, GOBP_G_PROTEIN_COUPLED_RECEPTOR_SIGNALING_PATHWAY, GOBP_DETECTION_OF_STIMULUS_INVOLVED_IN_SENSORY_PERCEPTION, KAECH_NAIVE_VS_DAY15_EFF_CD8_TCELL_UP, ZNF274_TARGET_GENES, REACTOME_OLFACTORY_SIGNALING_PATHWAY, REACTOME_SENSORY_PERCEPTION, GOBP_DETECTION_OF_CHEMICAL_STIMULUS

GO Biological Process (4): signal transduction (GO:0007165), G protein-coupled receptor signaling pathway (GO:0007186), sensory perception of smell (GO:0007608), detection of chemical stimulus involved in sensory perception of smell (GO:0050911)

GO Molecular Function (2): G protein-coupled receptor activity (GO:0004930), olfactory receptor activity (GO:0004984)

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

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
Olfactory Signaling Pathway1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
transmembrane signaling receptor activity2
cell communication1
cellular process1
signaling1
regulation of cellular process1
cellular response to stimulus1
G protein-coupled receptor activity1
signal transduction1
sensory perception of chemical stimulus1
sensory perception of smell1
detection of chemical stimulus involved in sensory perception1
G protein-coupled receptor signaling pathway1
detection of chemical stimulus involved in sensory perception of smell1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

342 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR4C3ZNF717Q9BY31577
OR4C3SPATA17Q96L03447
OR4C3UBTFL1P0CB47400
OR4C3ZNF781Q8N8C0380
OR4C3SAXO1Q8IYX7379
OR4C3CFAP65Q6ZU64374
OR4C3FRG2CA6NGY1371
OR4C3POM121L12Q8N7R1370
OR4C3GPR107Q5VW38364
OR4C3ARHGEF33A8MVX0364
OR4C3GAL3ST3Q96A11359
OR4C3PLEKHG4BQ96PX9356
OR4C3LRFN5Q96NI6355
OR4C3RCAN1P53805353
OR4C3LYARQ9NX58344

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A096LPK9, A0A0X1KG70, A6NHA9, A6NMZ5, P0C604, P0C623, P0C645, P0DN82, P58180, P58182, Q15615, Q60878, Q60881, Q6IEV9, Q6IF82, Q7TQQ0, Q8IXE1, Q8N0Y3, Q8NGB2, Q8NGB4, Q8NGB6, Q8NGC2, Q8NGD0, Q8NGD1, Q8NGF8, Q8NGF9, Q8NGI4, Q8NGI6, Q8NGJ1, Q8NGL6, Q8NGL7, Q8NGL9, Q8NGM1, Q8NGM8, Q8NGN0, Q8NGN8, Q8NGP0, Q8NH05, Q8NH37, Q8NH42

Diamond homologs: A0A096LPK9, A0A0X1KG70, A6NHA9, A6NMZ5, O60412, O76099, O95013, P0C604, P0C623, P0C645, P0DN82, P23270, P23275, P58173, P58180, P58182, Q15615, Q60878, Q60881, Q60888, Q6IEV9, Q6IEY1, Q6IF82, Q7TQQ0, Q8IXE1, Q8N0Y3, Q8N628, Q8NGA8, Q8NGB2, Q8NGB4, Q8NGB6, Q8NGB8, Q8NGB9, Q8NGC2, Q8NGC3, Q8NGC4, Q8NGC6, Q8NGD0, Q8NGD1, Q8NGD2

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

151 predictions. Top by Δscore:

VariantEffectΔscore
11:48325245:T:Gacceptor_gain0.8600
11:48325244:AT:Aacceptor_gain0.8500
11:48325245:T:TAacceptor_gain0.8300
11:48325244:ATG:Aacceptor_gain0.7700
11:48325244:A:AGacceptor_gain0.7500
11:48325246:G:Aacceptor_gain0.7100
11:48325079:GAG:Gdonor_gain0.6500
11:48325569:T:Aacceptor_gain0.6400
11:48325077:CAGAG:Cdonor_loss0.6300
11:48325078:AGAG:Adonor_loss0.6300
11:48325079:GAGGT:Gdonor_loss0.6300
11:48325080:AGGT:Adonor_loss0.6300
11:48325081:GGT:Gdonor_loss0.6300
11:48325082:GT:Gdonor_loss0.6300
11:48325083:T:Adonor_loss0.6300
11:48325656:T:Aacceptor_gain0.5600
11:48325608:T:Aacceptor_gain0.5100
11:48325082:G:GGdonor_gain0.4800
11:48325690:G:GCacceptor_gain0.4700
11:48325653:T:Gacceptor_gain0.4600
11:48325079:G:GTdonor_gain0.4200
11:48325876:T:Gacceptor_gain0.4200
11:48325568:CTGGA:Cacceptor_gain0.4000
11:48325254:A:Gacceptor_gain0.3900
11:48325689:TGAGG:Tacceptor_gain0.3900
11:48325253:A:AGacceptor_gain0.3800
11:48325084:A:Cdonor_loss0.3600
11:48325652:ATGCT:Aacceptor_gain0.3600
11:48325652:AT:Aacceptor_gain0.3500
11:48325817:GACAA:Gacceptor_gain0.3400

AlphaMissense

1972 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:48325544:T:CF175L0.900
11:48325546:T:AF175L0.900
11:48325546:T:GF175L0.900
11:48325517:T:CF166L0.880
11:48325519:C:AF166L0.880
11:48325519:C:GF166L0.880
11:48325049:T:CF10L0.863
11:48325051:T:AF10L0.863
11:48325051:T:GF10L0.863
11:48325319:T:CF100L0.784
11:48325321:T:AF100L0.784
11:48325321:T:GF100L0.784
11:48325106:T:CF29L0.740
11:48325108:T:AF29L0.740
11:48325108:T:GF29L0.740
11:48325766:T:CF249L0.697
11:48325768:T:AF249L0.697
11:48325768:T:GF249L0.697
11:48325763:T:CF248L0.680
11:48325765:C:AF248L0.680
11:48325765:C:GF248L0.680
11:48325622:A:CS201R0.654
11:48325624:T:AS201R0.654
11:48325624:T:GS201R0.654
11:48325460:T:AW147R0.643
11:48325460:T:CW147R0.643
11:48325781:T:CF254L0.642
11:48325783:T:AF254L0.642
11:48325783:T:GF254L0.642
11:48325646:T:CF209L0.638

dbSNP variants (sampled 300 via entrez): RS1000777353 (11:48323287 T>C), RS1003292417 (11:48324823 C>T), RS1003585872 (11:48324574 G>A), RS1004143127 (11:48326225 A>G), RS1005137673 (11:48325132 T>C,G), RS1005189833 (11:48324877 G>A), RS1006138825 (11:48324016 C>A,T), RS1006189632 (11:48323789 G>C), RS1008398761 (11:48326274 G>A), RS1013868009 (11:48323321 G>C), RS1015776663 (11:48326073 T>A,C,G), RS1016564362 (11:48325144 G>C,T), RS1016784992 (11:48324888 G>A,C,T), RS1016835917 (11:48324622 A>C), RS1017567801 (11:48324025 A>G)

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
GCST010774_29Essential hypertension (time to event)3.000000e-08

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004918age at diagnosis

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

4 total (human), top 4 by PubMed support.

ChemicalActions (top 5)PubMed papers
CGP 52608affects binding, increases reaction1
Resveratrolaffects cotreatment, decreases expression1
Plant Extractsdecreases expression, affects cotreatment1
Aflatoxin B1decreases methylation1

Clinical trials (associated diseases)

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

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): essential hypertension