OR4C11

gene
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Summary

OR4C11 (olfactory receptor family 4 subfamily C member 11, HGNC:15167) is a protein-coding gene on chromosome 11q11, encoding Olfactory receptor 4C11 (Q6IEV9). 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 219429 — RefSeq curated summary.

At a glance

  • GWAS associations: 4
  • Clinical variants (ClinVar): 74 total
  • MANE Select transcript: NM_001004700

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:15167
Approved symbolOR4C11
Nameolfactory receptor family 4 subfamily C member 11
Location11q11
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000172188
Ensembl biotypeprotein_coding
Entrez219429

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000641580

RefSeq mRNA: 1 — MANE Select: NM_001004700 NM_001004700

CCDS: CCDS31503

Canonical transcript exons

ENST00000641580 — 4 exons

ExonStartEnd
ENSE000038115225560728755607645
ENSE000038120125560652255606679
ENSE000038123995560236055604417
ENSE000038127735560512655605287

Expression profiles

Bgee: expression breadth not_expressed, 0 present calls, max score 37.20.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
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
sural nerveUBERON:001548835.01gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
bone marrowUBERON:000237131.74gold quality
muscle tissueUBERON:000238531.06gold quality
stromal cell of endometriumCL:000225529.87gold quality
prefrontal cortexUBERON:000045129.20gold quality
urinary bladderUBERON:000125528.47gold quality
liverUBERON:000210728.28gold quality
duodenumUBERON:000211428.14gold quality
lymph nodeUBERON:000002927.57gold quality
leukocyteCL:000073827.15gold quality
monocyteCL:000057627.10gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.90gold quality
vermiform appendixUBERON:000115426.42gold quality
bloodUBERON:000017826.22gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
muscle of legUBERON:000138324.96gold quality
primary visual cortexUBERON:000243624.61gold quality
pancreasUBERON:000126424.22gold quality
superior frontal gyrusUBERON:000266124.08gold quality
frontal cortexUBERON:000187024.07gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no2.12

Regulation

Is transcription factor: no

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
mus_musculusOr4c11cENSMUSG00000057447
mus_musculusOr4c11bENSMUSG00000059023
mus_musculusOr4c11ENSMUSG00000062757
rattus_norvegicusOr4c11ENSRNOG00000063322

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), OR4X2 (ENSG00000172208), OR4D9 (ENSG00000172742), OR10K1 (ENSG00000173285), OR1L1 (ENSG00000173679), OR7D4 (ENSG00000174667), OR4S2 (ENSG00000174982), OR4B1 (ENSG00000175619), OR4D11 (ENSG00000176200), OR4K17 (ENSG00000176230)

Protein

Protein identifiers

Olfactory receptor 4C11Q6IEV9 (reviewed: Q6IEV9)

Alternative names: Olfactory receptor OR11-136

All UniProt accessions (2): A0A126GVN6, Q6IEV9

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_001004700* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain
IPR050427Olfactory_ReceptorsFamily

Pfam: PF13853

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

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q6IEV9-F190.060.72

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): 4

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

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

MSigDB gene sets: 17 (showing top): GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, KEGG_OLFACTORY_TRANSDUCTION, GOBP_DETECTION_OF_STIMULUS, GOBP_SENSORY_PERCEPTION, CAMPS_COLON_CANCER_COPY_NUMBER_DN, 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, chr11q11, 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

216 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR4C11ZFP14Q9HCL3399
OR4C11FAM234BA2RU67393
OR4C11TRIM48Q8IWZ4377
OR4C11TRIM51Q9BSJ1368
OR4C11HSDL1Q3SXM5359
OR4C11ZNF41P51814349
OR4C11TMTC3Q6ZXV5348
OR4C11SPPL2CQ8IUH8305
OR4C11LILRB5O75023279
OR4C11CAPN7Q9Y6W3275
OR4C11UGT2B17O75795269
OR4C11ZNF737O75373264
OR4C11HPDLQ96IR7248
OR4C11ANKS1BQ7Z6G8247
OR4C11APOBEC3BQ9UH17230

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

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance65
Likely benign4
Benign5

Top pathogenic / likely-pathogenic (0)

SpliceAI

323 predictions. Top by Δscore:

VariantEffectΔscore
11:55604299:CA:Cdonor_gain0.8400
11:55604212:T:TAdonor_gain0.7900
11:55604291:A:ACdonor_gain0.7800
11:55604356:A:ACdonor_gain0.7100
11:55604357:C:CCdonor_gain0.7100
11:55604310:G:GAdonor_gain0.6700
11:55604355:CA:Cdonor_gain0.6400
11:55604298:A:ACdonor_gain0.6200
11:55604299:C:CCdonor_gain0.6200
11:55604295:CAAA:Cdonor_gain0.5900
11:55604294:A:ACdonor_gain0.5800
11:55604295:C:CCdonor_gain0.5800
11:55603608:A:Cacceptor_gain0.5600
11:55603610:A:Cacceptor_gain0.5600
11:55603834:C:CCacceptor_gain0.5500
11:55604167:AGAAT:Aacceptor_gain0.5500
11:55604204:A:Cdonor_gain0.5300
11:55603479:A:Cdonor_gain0.5200
11:55603706:A:Tacceptor_gain0.5200
11:55604321:T:TAdonor_gain0.5200
11:55603606:A:Cacceptor_gain0.5100
11:55603620:A:Cacceptor_gain0.5100
11:55603604:G:Cacceptor_gain0.5000
11:55603389:A:ACdonor_gain0.4900
11:55603390:C:CCdonor_gain0.4900
11:55603502:T:TAdonor_gain0.4800
11:55603704:TCA:Tacceptor_gain0.4800
11:55604199:A:ACdonor_gain0.4800
11:55604297:A:Tdonor_gain0.4800
11:55603411:C:CCacceptor_gain0.4700

AlphaMissense

2049 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:55603876:G:CF166L0.876
11:55603876:G:TF166L0.876
11:55603878:A:GF166L0.876
11:55603750:A:CS208R0.874
11:55603750:A:TS208R0.874
11:55603752:T:GS208R0.874
11:55604344:G:CF10L0.858
11:55604344:G:TF10L0.858
11:55604346:A:GF10L0.858
11:55604074:A:CF100L0.801
11:55604074:A:TF100L0.801
11:55604076:A:GF100L0.801
11:55603627:A:CF249L0.784
11:55603627:A:TF249L0.784
11:55603629:A:GF249L0.784
11:55604166:A:GC70R0.782
11:55603935:A:GW147R0.778
11:55603935:A:TW147R0.778
11:55604059:A:CF105L0.746
11:55604059:A:TF105L0.746
11:55604061:A:GF105L0.746
11:55603753:A:CS207R0.744
11:55603753:A:TS207R0.744
11:55603755:T:GS207R0.744
11:55603612:G:CF254L0.729
11:55603612:G:TF254L0.729
11:55603614:A:GF254L0.729
11:55604147:G:TA76D0.721
11:55604026:C:AM116I0.720
11:55604026:C:GM116I0.720

dbSNP variants (sampled 300 via entrez): RS1000940599 (11:55602422 C>T), RS1001289362 (11:55602780 A>G), RS1001894142 (11:55605212 A>C), RS1002346667 (11:55604622 G>C), RS1005124546 (11:55606977 A>C), RS1005861055 (11:55608813 T>G), RS1006745101 (11:55603508 T>C), RS1006798859 (11:55603001 G>T), RS1011690000 (11:55607795 A>G), RS1012169024 (11:55602293 AAAT>A), RS1013174263 (11:55604570 C>A,T), RS1014597533 (11:55609007 CCCT>C), RS1014630021 (11:55608307 A>G), RS1014664210 (11:55607863 C>A,T), RS1017832279 (11:55605752 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

4 associations (top):

StudyTraitp-value
GCST007094_101Diastolic blood pressure4.000000e-06
GCST007095_40Systolic blood pressure4.000000e-07
GCST007095_41Systolic blood pressure1.000000e-06
GCST007099_2Systolic blood pressure5.000000e-08

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0006336diastolic blood pressure
EFO:0006335systolic blood pressure

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

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.