OR4A15

gene
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Summary

OR4A15 (olfactory receptor family 4 subfamily A member 15, HGNC:15152) is a protein-coding gene on chromosome 11q11, encoding Olfactory receptor 4A15 (Q8NGL6). 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 81328 — RefSeq curated summary.

At a glance

  • GWAS associations: 6
  • Clinical variants (ClinVar): 125 total
  • MANE Select transcript: NM_001005275

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:15152
Approved symbolOR4A15
Nameolfactory receptor family 4 subfamily A member 15
Location11q11
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000181958
Ensembl biotypeprotein_coding
Entrez81328

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000641526

RefSeq mRNA: 1 — MANE Select: NM_001005275 NM_001005275

CCDS: CCDS31500

Canonical transcript exons

ENST00000641526 — 1 exons

ExonStartEnd
ENSE000038126975536797455368918

Expression profiles

Bgee: expression breadth not_expressed, 0 present calls, max score 37.94.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
granulocyteCL:000009437.94gold quality
colonic epitheliumUBERON:000039737.20gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
skeletal muscle tissueUBERON:000113435.68gold quality
ganglionic eminenceUBERON:000402335.49gold quality
muscle tissueUBERON:000238532.75gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
bone marrowUBERON:000237131.74gold quality
sural nerveUBERON:001548830.93gold quality
stromal cell of endometriumCL:000225529.87gold quality
liverUBERON:000210729.19gold quality
prefrontal cortexUBERON:000045129.04gold quality
duodenumUBERON:000211428.14gold quality
leukocyteCL:000073828.05gold quality
right coronary arteryUBERON:000162527.90gold quality
lymph nodeUBERON:000002927.57gold quality
monocyteCL:000057627.43gold quality
urinary bladderUBERON:000125527.09gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.55gold quality
vermiform appendixUBERON:000115426.42gold quality
bloodUBERON:000017826.33gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
right lobe of liverUBERON:000111425.35gold quality
calcaneal tendonUBERON:000370125.06gold quality
muscle of legUBERON:000138324.94gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.98

Regulation

Is transcription factor: no

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
mus_musculusOr4a15ENSMUSG00000075090
rattus_norvegicusOr4a15bENSRNOG00000064878
rattus_norvegicusOr4a15ENSRNOG00000086694

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 4A15Q8NGL6 (reviewed: Q8NGL6)

Alternative names: Olfactory receptor OR11-118

All UniProt accessions (1): A0A286YF59

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_001005275* (*=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, glycosylation site 2, sequence variant 2, chain 1, disulfide bond 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8NGL6-F185.020.58

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): 125–217

Glycosylation sites (2): 36, 290

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, ACEVEDO_LIVER_CANCER_WITH_H3K27ME3_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

250 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR4A15TRIM48Q8IWZ4448
OR4A15TRIM51Q9BSJ1445
OR4A15ZNF737O75373336
OR4A15CFAP47Q6ZTR5270
OR4A15POTEMA6NI47264
OR4A15VWA3BQ502W6249
OR4A15TM4SF20Q53R12220
OR4A15CHCHD5Q9BSY4213
OR4A15NPIPA5E9PKD4204
OR4A15ZNF277Q9NRM2203
OR4A15FRMD1Q8N878202
OR4A15NPIPA3F8WFD2202
OR4A15KIF25Q9UIL4202
OR4A15CEP20Q96NB1199
OR4A15ZNF385DQ9H6B1192

IntAct

2 interactions, top by confidence:

ABTypeScore
OR4D2EEF1A2psi-mi:“MI:0914”(association)0.350

BioGRID (2): OR4A15 (Affinity Capture-MS), OR4A15 (Affinity Capture-MS)

ESM2 similar proteins: A0A096LPK9, A0A0X1KG70, A6NHA9, A6NMZ5, P0C604, P0C623, P0C645, P0DN82, P58180, P58182, Q15615, Q60881, Q6IF82, Q8IXE1, Q8N0Y3, Q8NGA8, Q8NGB4, Q8NGB6, Q8NGC2, Q8NGC3, Q8NGD0, Q8NGD1, Q8NGD2, Q8NGD5, Q8NGE8, Q8NGF4, Q8NGF8, Q8NGF9, Q8NGI4, Q8NGI6, Q8NGJ0, Q8NGJ1, Q8NGL6, Q8NGM1, Q8NGN0, Q8NGN8, Q8NGX5, Q8NH05, Q8NH42, Q8NH49

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

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance114
Likely benign10
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

259 predictions. Top by Δscore:

VariantEffectΔscore
11:55367996:C:Gdonor_gain0.7800
11:55367981:A:AGdonor_gain0.7200
11:55368291:T:Aacceptor_gain0.6300
11:55367991:T:Gdonor_gain0.5800
11:55368143:T:Gdonor_gain0.5500
11:55368002:T:Gdonor_gain0.5300
11:55368046:T:TGdonor_gain0.5200
11:55368347:G:GGdonor_gain0.5200
11:55368147:C:CGdonor_gain0.5100
11:55368419:G:GTdonor_gain0.5000
11:55368741:T:Gacceptor_gain0.4900
11:55368883:G:GGdonor_gain0.4700
11:55367995:A:AGdonor_gain0.4600
11:55368002:T:TGdonor_gain0.4600
11:55368315:G:GAdonor_gain0.4600
11:55368344:TCT:Tdonor_gain0.4600
11:55368628:A:AGdonor_gain0.4500
11:55367992:G:GGdonor_gain0.4400
11:55368044:T:TAdonor_gain0.4400
11:55368319:A:AGdonor_gain0.4400
11:55368035:G:Tdonor_gain0.4300
11:55368461:A:AGacceptor_gain0.4300
11:55368462:G:GGacceptor_gain0.4300
11:55368148:T:Gdonor_gain0.4200
11:55368705:G:GAdonor_gain0.4200
11:55368812:T:Aacceptor_gain0.4200
11:55368045:T:Adonor_gain0.4100
11:55368314:T:TAdonor_gain0.4100
11:55368626:T:TAdonor_gain0.4100
11:55368641:T:Gdonor_gain0.4100

AlphaMissense

2067 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:55368001:T:CF40L0.956
11:55368003:T:AF40L0.956
11:55368003:T:GF40L0.956
11:55368469:T:CF196L0.953
11:55368471:C:AF196L0.953
11:55368471:C:GF196L0.953
11:55368002:T:CF40S0.951
11:55368002:T:GF40C0.895
11:55368502:T:AC207S0.886
11:55368503:G:CC207S0.886
11:55368470:T:GF196C0.883
11:55368496:T:CF205L0.866
11:55368498:C:AF205L0.866
11:55368498:C:GF205L0.866
11:55368470:T:CF196S0.857
11:55368256:T:AC125S0.843
11:55368257:G:CC125S0.843
11:55368502:T:CC207R0.830
11:55368258:T:GC125W0.816
11:55368271:T:CF130L0.796
11:55368273:T:AF130L0.796
11:55368273:T:GF130L0.796
11:55368058:T:CF59L0.786
11:55368060:C:AF59L0.786
11:55368060:C:GF59L0.786
11:55368256:T:CC125R0.786
11:55368518:T:CL212S0.781
11:55368504:T:GC207W0.767
11:55368534:C:GC217W0.767
11:55368503:G:AC207Y0.747

dbSNP variants (sampled 300 via entrez): RS1000603929 (11:55366515 A>C), RS1000619835 (11:55367305 T>C), RS1000903120 (11:55366676 T>C), RS1006510539 (11:55366085 C>A), RS1006806797 (11:55366217 G>T), RS1007018790 (11:55367615 A>G,T), RS1007468895 (11:55367101 A>G), RS1007544470 (11:55367762 C>A,G,T), RS1010479314 (11:55367515 A>G), RS1010925704 (11:55369232 G>A,T), RS1011990809 (11:55366277 G>A), RS1014167901 (11:55367151 T>G), RS1014282484 (11:55367284 A>G,T), RS1016728012 (11:55366729 G>T), RS1017319439 (11:55367538 T>C)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (1): primary ovarian failure (MONDO:0005387)

Orphanet (1): NON RARE IN EUROPE: Primary ovarian failure (Orphanet:619)

HPO phenotypes

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

GWAS associations

6 associations (top):

StudyTraitp-value
GCST000996_14Systemic lupus erythematosus7.000000e-06
GCST005580_74Intraocular pressure1.000000e-11
GCST007267_72Systolic blood pressure7.000000e-09
GCST007928_83Medication use (diuretics)1.000000e-08
GCST008058_10Estimated glomerular filtration rate1.000000e-09
GCST008060_10Estimated glomerular filtration rate3.000000e-08

EFO canonical traits (3, from GWAS)

EFO IDTrait name
EFO:0004695intraocular pressure measurement
EFO:0006335systolic blood pressure
EFO:0009928Diuretic use measurement

MeSH disease descriptors (1)

DescriptorNameTree numbers
D016649Primary Ovarian InsufficiencyC12.050.351.500.056.630.750; C12.100.250.056.630.750; C19.391.630.750

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

2 total (human), top 2 by PubMed support.

ChemicalActions (top 5)PubMed papers
CGP 52608increases reaction, affects binding1
Benzo(a)pyreneaffects methylation1

Clinical trials (associated diseases)

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

TrialPhaseStatusTitle
NCT00417066PHASE4COMPLETEDFlexible GnRH Antagonist vs Flare up GnRH Agonist Protocol in Poor Responders
NCT00732693PHASE4COMPLETEDEvaluation of Physiologic and Standard Sex Steroid Replacement Regimens in Women With Premature Ovarian Failure
NCT00837616PHASE4COMPLETEDEstrogen Dosing in Turner Syndrome: Pharmacology and Metabolism
NCT01853501PHASE4UNKNOWNEffects of ADSC Therapy in Women With POF
NCT02783937PHASE4COMPLETEDFilgrastim for Premature Ovarian Insufficiency
NCT03535480PHASE4UNKNOWNAutologous Bone Marrow Stem Cell Ovarian Transplantation to Restore Ovarian Function in Premature Ovarian Failure
NCT00140998PHASE3COMPLETEDEstrogen Treatment (Oral vs. Patches) in Turner Syndrome
NCT00001951PHASE2COMPLETEDHormone Replacement in Young Women With Premature Ovarian Failure
NCT00370019PHASE2WITHDRAWNEffects of an Estrogen Replacement Therapy Skin Patch on Ovulation in Women With Premature Ovarian Failure
NCT00429494PHASE2COMPLETEDGnRH Analogue for Ovarian Function Preservation in Hematopoietic Stem Cell Transplantation Patients
NCT03816852PHASE2SUSPENDEDThe Safety and Efficiency Study of Mesenchymal Stem Cell (19#iSCLife®-POI) in Premature Ovarian Insufficiency
NCT04536467PHASE2UNKNOWNPrevention of Chemotherapy-Induced Ovarian Failure With Goserelin in Premenopausal Lymphoma Patients
NCT06117982PHASE2COMPLETEDThe Impact of Granulocyte Colony Stimulating Factor on Premature Ovarian Insufficiency
NCT02912104PHASE1COMPLETEDA Therapeutic Trial of Human Amniotic Epithelial Cells Transplantation for Primary Ovarian Failure
NCT03178695PHASE1COMPLETEDInovium Ovarian Rejuvenation Trials
NCT04815213PHASE1ACTIVE_NOT_RECRUITINGThe Use of Expandeded Mesenchymal Stromal Cells (MSC) in Premature Ovarian Failure (POF) in Adult Humans
NCT05138367PHASE1COMPLETEDEffects of UCA-PSCs in Women With POF
NCT06132542PHASE1UNKNOWNAutologous ADMSC Transplantation in Patients With POI
NCT00948857PHASE2/PHASE3TERMINATEDDehydroepiandrosterone (DHEA) Treatment and Premature Ovarian Failure (POF)
NCT04031456PHASE2/PHASE3RECRUITINGAutologous PRP Infusion May Restore Ovarian Function and May Promote Folliculogenesis in POI Patients
NCT02043743PHASE1/PHASE2UNKNOWNAutologous Stem Cells Transplantation in Patients With Idiopathic and Drug Induced Premature Ovarian Failure
NCT02062931PHASE1/PHASE2UNKNOWNAutologous Mesenchymal Stem Cells Transplantation In Women With Premature Ovarian Failure
NCT02151890PHASE1/PHASE2COMPLETEDPregnancy After Stem Cell Transplantation in Premature Ovarian Failure
NCT02372474PHASE1/PHASE2COMPLETEDIt is a Real The First Baby Of Autologous Stem Cell Therapy in Premature Ovarian Failure
NCT02603744PHASE1/PHASE2UNKNOWNAutologous Adipose Derived Mesenchymal Stromal Cells Transplantation in Women With Premature Ovarian Failure (POF)
NCT02644447PHASE1/PHASE2COMPLETEDTransplantation of HUC-MSCs With Injectable Collagen Scaffold for POF
NCT03069209PHASE1/PHASE2UNKNOWNAutologous Bone Marrow-Derived Stem Cell Transplantation in Patients With Premature Ovarian Failure (POF)
NCT03985462PHASE1/PHASE2WITHDRAWNVery Small Embryonic-like Stem Cells for Ovary
NCT04009473PHASE1/PHASE2UNKNOWNStem Cell Therapy and Growth Factor Ovarian in Vitro Activation
NCT04071574PHASE1/PHASE2COMPLETEDComparative Study on the Efficacy of Ovarian Stimulation Protocols on the Success Rate of ICSI in Female Infertility
NCT04922398PHASE1/PHASE2UNKNOWNOvarian Injection of PRP (Platelet -Rich Plasma) Vs Normal Saline in Premature Ovarian Insufficiency
NCT05462379PHASE1/PHASE2ACTIVE_NOT_RECRUITINGAutologous Heterotopic Fresh Ovarian Graft in Woman With LACC Eligible for Pelvic Radiotherapy Treatment.
NCT06202547PHASE1/PHASE2UNKNOWNIntra-ovarian Injection of MSC-EVs in Idiopathic Premature Ovarian Failure
NCT01129947EARLY_PHASE1WITHDRAWNThe Use of DHEA in Women With Premature Ovarian Failure
NCT05522634EARLY_PHASE1UNKNOWNA Clinical Study of Chinese Herbal Compound TJAOA101 in the Treatment of Premature Ovarian Insufficiency
NCT07308327EARLY_PHASE1ACTIVE_NOT_RECRUITINGThe Influence of Gut Microbiota on Ovarian Function: A Single-center, Randomized,Double Blind, Parallel-controlled, Exploratory Clinical Trial
NCT00001275Not specifiedCOMPLETEDOvarian Follicle Function in Patients With Primary Ovarian Failure
NCT00001306Not specifiedCOMPLETEDSteroid Therapy in Autoimmune Premature Ovarian Failure
NCT00006156Not specifiedCOMPLETEDFeasibility Study for Development of an Early Test for Ovarian Failure
NCT00119925Not specifiedUNKNOWN‘SPRING’-Study: Subfertility Guidelines: Patient Related Implementation in the Netherlands Among Gynaecologists
  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): primary ovarian failure