OR2L3

gene
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Summary

OR2L3 (olfactory receptor family 2 subfamily L member 3, HGNC:15009) is a protein-coding gene on chromosome 1q44, encoding Olfactory receptor 2L3 (Q8NG85). 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 391192 — RefSeq curated summary.

At a glance

  • MANE Select transcript: NM_001004687

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:15009
Approved symbolOR2L3
Nameolfactory receptor family 2 subfamily L member 3
Location1q44
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000198128
Ensembl biotypeprotein_coding
Entrez391192

Gene structure

Transcript identifiers

Ensembl transcripts: 3 — 3 protein_coding

ENST00000359959, ENST00000641161, ENST00000641649

RefSeq mRNA: 1 — MANE Select: NM_001004687 NM_001004687

CCDS: CCDS31104

Canonical transcript exons

ENST00000359959 — 2 exons

ExonStartEnd
ENSE00002392655248060661248063407
ENSE00003813392248046836248046880

Expression profiles

Bgee: expression breadth broad, 19 present calls, max score 54.82.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
cortical plateUBERON:000534354.82silver quality
sural nerveUBERON:001548846.53gold quality
ventricular zoneUBERON:000305344.20silver quality
primary visual cortexUBERON:000243644.12silver quality
prefrontal cortexUBERON:000045143.93silver quality
C1 segment of cervical spinal cordUBERON:000646943.56gold quality
ganglionic eminenceUBERON:000402342.58gold quality
bone marrow cellCL:000209240.51gold quality
Brodmann (1909) area 9UBERON:001354040.38silver quality
calcaneal tendonUBERON:000370140.29gold quality
frontal cortexUBERON:000187040.21silver quality
monocyteCL:000057639.97gold quality
cerebellar cortexUBERON:000212939.50silver quality
smooth muscle tissueUBERON:000113539.33silver quality
cerebellumUBERON:000203739.33silver quality
leukocyteCL:000073838.86gold quality
substantia nigraUBERON:000203838.70gold quality
dorsolateral prefrontal cortexUBERON:000983438.60silver quality
hypothalamusUBERON:000189838.56silver quality
right hemisphere of cerebellumUBERON:001489038.41silver quality
apex of heartUBERON:000209838.21silver quality
corpus callosumUBERON:000233637.77gold quality
bloodUBERON:000017837.64gold quality
lower esophagus mucosaUBERON:003583437.37gold quality
Ammon’s hornUBERON:000195437.33silver quality
bone marrowUBERON:000237137.31gold quality
colonic epitheliumUBERON:000039737.20gold quality
muscle tissueUBERON:000238536.96gold quality
endometriumUBERON:000129536.52gold quality
amygdalaUBERON:000187636.25silver quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes3.12

Regulation

Is transcription factor: no

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusOr2l5ENSMUSG00000045341
rattus_norvegicusOr2l5ENSRNOG00000081703

Paralogs (92): OR2B6 (ENSG00000124657), OR13C9 (ENSG00000136839), OR13C4 (ENSG00000148136), OR2M5 (ENSG00000162727), OR10A5 (ENSG00000166363), OR2D2 (ENSG00000166368), OR2B2 (ENSG00000168131), OR2C1 (ENSG00000168158), OR13J1 (ENSG00000168828), OR10G3 (ENSG00000169208), OR10A3 (ENSG00000170683), OR10A4 (ENSG00000170782), OR10A2 (ENSG00000170790), OR13H1 (ENSG00000171054), OR2K2 (ENSG00000171133), OR2M4 (ENSG00000171180), OR10H2 (ENSG00000171942), OR10H5 (ENSG00000172519), OR10AD1 (ENSG00000172640), OR2Y1 (ENSG00000174339), OR10AG1 (ENSG00000174970), OR2T1 (ENSG00000175143), OR10P1 (ENSG00000175398), OR2T35 (ENSG00000177151), OR2M7 (ENSG00000177186), OR2T12 (ENSG00000177201), OR2T33 (ENSG00000177212), OR2AJ1 (ENSG00000177275), OR2T8 (ENSG00000177462), OR2G3 (ENSG00000177476), OR2G2 (ENSG00000177489), OR2B11 (ENSG00000177535), OR2D3 (ENSG00000178358), OR13D1 (ENSG00000179055), OR10A7 (ENSG00000179919), OR2Z1 (ENSG00000181733), OR2V2 (ENSG00000182613), OR10G7 (ENSG00000182634), OR2T29 (ENSG00000182783), OR2T34 (ENSG00000183310)

Protein

Protein identifiers

Olfactory receptor 2L3Q8NG85 (reviewed: Q8NG85)

All UniProt accessions (1): Q8NG85

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_001004687* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain

Pfam: PF13853

UniProt features (23 total): topological domain 8, transmembrane region 7, sequence variant 4, glycosylation site 2, chain 1, disulfide bond 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8NG85-F191.360.77

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): 96–188

Glycosylation sites (2): 5, 88

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, chr1q44, 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, SRPK2_TARGET_GENES, REACTOME_OLFACTORY_SIGNALING_PATHWAY, REACTOME_SENSORY_PERCEPTION, GOBP_DETECTION_OF_CHEMICAL_STIMULUS

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

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
sensory perception of smell1
detection of chemical stimulus involved in sensory perception1
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
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

104 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR2L3AK9Q5TCS8419
OR2L3PLBD1Q6P4A8368
OR2L3MMABQ96EY8358
OR2L3SLC22A10Q63ZE4353
OR2L3MAGEB16A2A368353
OR2L3SLC22A24Q8N4F4353
OR2L3MMS22LQ6ZRQ5351
OR2L3DEGS2Q6QHC5329
OR2L3FXYD3Q14802317
OR2L3IQGAP3Q86VI3311
OR2L3TMEM244Q5VVB8311
OR2L3CDONQ4KMG0287
OR2L3DYNC2H1Q8NCM8279
OR2L3NUP210Q8TEM1271
OR2L3RYR3Q15413222

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A3KFT3, P0C628, P34982, P34985, P37068, P37071, Q15612, Q60879, Q8N146, Q8N162, Q8N349, Q8NG80, Q8NG81, Q8NG83, Q8NG85, Q8NG92, Q8NG95, Q8NGA1, Q8NGC7, Q8NGC8, Q8NGC9, Q8NGE0, Q8NGG4, Q8NGI8, Q8NGQ6, Q8NGS4, Q8NGY6, Q8NGY9, Q8NGZ0, Q8NGZ9, Q8NH16, Q8NH74, Q8NHA4, Q8NHB7, Q8NHC8, Q8VEX5, Q8VFR8, Q8VFV4, Q8VFX2, Q8VGI4

Diamond homologs: A3KFT3, A4D2G3, A6NH00, A6NL26, A6NM03, O43869, O76000, O76001, O76002, O95006, O95221, O95371, O95918, P0C7N1, P0C7T2, P23274, P23275, P34984, P59922, Q13606, Q13607, Q5TZ20, Q60880, Q60890, Q6IEZ7, Q6IF00, Q8N127, Q8N349, Q8N628, Q8NG75, Q8NG76, Q8NG77, Q8NG80, Q8NG81, Q8NG83, Q8NG84, Q8NG85, Q8NG97, Q8NGC0, Q8NGE5

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

630 predictions. Top by Δscore:

VariantEffectΔscore
1:248046983:A:Gdonor_gain0.9200
1:248051242:G:GGdonor_gain0.8900
1:248047783:GT:Gdonor_gain0.8400
1:248048499:G:GTdonor_gain0.8400
1:248053058:GTAT:Gdonor_gain0.8300
1:248053059:TATT:Tdonor_gain0.8300
1:248053060:ATTA:Adonor_gain0.8300
1:248061564:G:GTdonor_gain0.8100
1:248047636:G:Aacceptor_gain0.8000
1:248053061:T:TGdonor_gain0.8000
1:248047635:C:CAacceptor_gain0.7900
1:248061588:G:GGdonor_gain0.7900
1:248051186:AG:Aacceptor_gain0.7800
1:248051187:GG:Gacceptor_gain0.7800
1:248055340:C:Adonor_gain0.7600
1:248061586:GA:Gdonor_gain0.7400
1:248048465:G:GTdonor_gain0.7300
1:248061324:T:Gacceptor_gain0.7300
1:248061451:C:Gacceptor_gain0.7200
1:248061449:C:Gacceptor_gain0.7000
1:248052963:TTAAG:Tacceptor_gain0.6900
1:248052964:TAAGT:Tacceptor_gain0.6900
1:248061323:AT:Aacceptor_gain0.6900
1:248061332:T:Gacceptor_gain0.6900
1:248061323:A:AGacceptor_gain0.6800
1:248061005:TGCAG:Tdonor_gain0.6700
1:248061314:T:TAacceptor_gain0.6700
1:248061450:A:AGacceptor_gain0.6700
1:248061570:A:AGdonor_gain0.6700
1:248052965:AAG:Aacceptor_gain0.6600

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000208081 (1:248060682 A>G), RS1000264473 (1:248054437 C>G), RS1000371688 (1:248048191 C>T), RS1000541941 (1:248061924 T>A), RS1000651166 (1:248055607 AT>A), RS1000707841 (1:248049700 C>T), RS1000722233 (1:248054128 T>C), RS1001122768 (1:248046661 T>C), RS1001175080 (1:248046390 A>G), RS1001597951 (1:248048622 C>T), RS1001866091 (1:248060170 C>A), RS1001887397 (1:248056287 AT>A,ATT), RS1001908278 (1:248055186 A>T), RS1001964548 (1:248049810 A>T), RS1002172149 (1:248044933 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

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

5 total (human), top 5 by PubMed support.

ChemicalActions (top 5)PubMed papers
mancozebdecreases expression1
CGP 52608affects binding, increases reaction1
(+)-JQ1 compoundincreases expression1
Arsenicaffects methylation1
Niclosamidedecreases expression1

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.