OR2T6
gene geneOn this page
Also known as OST703
Summary
OR2T6 (olfactory receptor family 2 subfamily T member 6, HGNC:15018) is a protein-coding gene on chromosome 1q44, encoding Olfactory receptor 2T6 (Q8NHC8). 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 254879 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 51 total
- MANE Select transcript:
NM_001005471
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:15018 |
| Approved symbol | OR2T6 |
| Name | olfactory receptor family 2 subfamily T member 6 |
| Location | 1q44 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | OST703 |
| Ensembl gene | ENSG00000198104 |
| Ensembl biotype | protein_coding |
| Entrez | 254879 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000641644
RefSeq mRNA: 1 — MANE Select: NM_001005471
NM_001005471
CCDS: CCDS31114
Canonical transcript exons
ENST00000612137 — 0 exons
Expression profiles
Bgee: expression breadth tissue_specific, 4 present calls, max score 52.79.
Top tissues by expression
109 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 52.79 | silver quality |
| sural nerve | UBERON:0015488 | 46.14 | gold quality |
| colonic epithelium | UBERON:0000397 | 42.88 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 41.67 | gold quality |
| ventricular zone | UBERON:0003053 | 39.84 | gold quality |
| primary visual cortex | UBERON:0002436 | 39.00 | gold quality |
| ganglionic eminence | UBERON:0004023 | 38.79 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 36.37 | silver quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| bone marrow | UBERON:0002371 | 34.97 | gold quality |
| monocyte | CL:0000576 | 34.43 | gold quality |
| leukocyte | CL:0000738 | 33.81 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 33.40 | silver quality |
| skeletal muscle tissue | UBERON:0001134 | 33.38 | gold quality |
| kidney | UBERON:0002113 | 33.03 | silver quality |
| putamen | UBERON:0001874 | 32.70 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| cortex of kidney | UBERON:0001225 | 31.48 | gold quality |
| nucleus accumbens | UBERON:0001882 | 31.46 | gold quality |
| muscle tissue | UBERON:0002385 | 31.06 | gold quality |
| right lung | UBERON:0002167 | 30.33 | gold quality |
| calcaneal tendon | UBERON:0003701 | 30.06 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| endometrium | UBERON:0001295 | 29.48 | gold quality |
| heart left ventricle | UBERON:0002084 | 29.44 | gold quality |
| liver | UBERON:0002107 | 28.75 | gold quality |
| lymph node | UBERON:0000029 | 28.68 | gold quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| blood | UBERON:0000178 | 27.93 | gold quality |
Single-cell (SCXA)
Detected in 2 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-MTAB-7249 | no | 2.62 |
| E-ANND-3 | no | 0.05 |
Regulation
Is transcription factor: no
Cross-species orthologs
2 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Or2t6 | ENSMUSG00000052417 |
| rattus_norvegicus | Or2t6 | ENSRNOG00000084296 |
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 2T6 — Q8NHC8 (reviewed: Q8NHC8)
Alternative names: OST703, Olfactory receptor 2T9
All UniProt accessions (1): Q8NHC8
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_001005471* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR000276 | GPCR_Rhodpsn | Family |
| IPR000725 | Olfact_rcpt | Family |
| IPR017452 | GPCR_Rhodpsn_7TM | Domain |
Pfam: PF13853
UniProt features (23 total): topological domain 8, transmembrane region 7, sequence variant 5, chain 1, glycosylation site 1, disulfide bond 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q8NHC8-F1 | 88.18 | 0.57 |
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): 97–179
Glycosylation sites (1): 5
Function
Pathways and Gene Ontology
Reactome pathways
1 pathways
| ID | Pathway |
|---|---|
| R-HSA-9752946 | Expression 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, REACTOME_OLFACTORY_SIGNALING_PATHWAY, REACTOME_SENSORY_PERCEPTION, GOBP_DETECTION_OF_CHEMICAL_STIMULUS, GOMF_MOLECULAR_TRANSDUCER_ACTIVITY
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:
| Category | Pathways |
|---|---|
| Olfactory Signaling Pathway | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| transmembrane signaling receptor activity | 2 |
| sensory perception of smell | 1 |
| detection of chemical stimulus involved in sensory perception | 1 |
| cell communication | 1 |
| cellular process | 1 |
| signaling | 1 |
| regulation of cellular process | 1 |
| cellular response to stimulus | 1 |
| G protein-coupled receptor activity | 1 |
| signal transduction | 1 |
| sensory perception of chemical stimulus | 1 |
| G protein-coupled receptor signaling pathway | 1 |
| detection of chemical stimulus involved in sensory perception of smell | 1 |
| membrane | 1 |
| cell periphery | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
120 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| OR2T6 | TAS2R42 | Q7RTR8 | 400 |
| OR2T6 | TRIM48 | Q8IWZ4 | 397 |
| OR2T6 | YPEL4 | Q96NS1 | 378 |
| OR2T6 | THSD7B | Q9C0I4 | 325 |
| OR2T6 | NLRP11 | P59045 | 313 |
| OR2T6 | INSL5 | Q9Y5Q6 | 287 |
| OR2T6 | LAIR2 | Q6ISS4 | 275 |
| OR2T6 | TMEM229A | B2RXF0 | 265 |
| OR2T6 | ATP6V0C | P27449 | 223 |
| OR2T6 | CXXC5 | Q7LFL8 | 220 |
| OR2T6 | GOLT1B | Q9Y3E0 | 214 |
| OR2T6 | OR51B4 | Q9Y5P0 | 212 |
| OR2T6 | MUC12 | Q9UKN1 | 204 |
| OR2T6 | ELOVL2 | Q9NXB9 | 184 |
| OR2T6 | PFKFB2 | O60825 | 183 |
IntAct
2 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| ALB | CDC45 | psi-mi:“MI:0914”(association) | 0.350 |
BioGRID (1): OR2T6 (Affinity Capture-MS)
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
51 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 47 |
| Likely benign | 4 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
373 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 1:248388098:A:G | donor_gain | 0.7800 |
| 1:248388098:A:AG | donor_gain | 0.7600 |
| 1:248388223:A:AG | acceptor_gain | 0.7200 |
| 1:248388243:C:CA | acceptor_gain | 0.7200 |
| 1:248388203:AT:A | donor_gain | 0.6900 |
| 1:248387974:C:G | donor_gain | 0.6700 |
| 1:248388146:G:GC | acceptor_gain | 0.6700 |
| 1:248388223:AAT:A | acceptor_gain | 0.6700 |
| 1:248388480:GTCT:G | acceptor_gain | 0.6600 |
| 1:248388145:T:TA | acceptor_gain | 0.6500 |
| 1:248388228:T:A | acceptor_gain | 0.6300 |
| 1:248388034:G:GT | donor_gain | 0.6200 |
| 1:248388246:T:TA | acceptor_gain | 0.6200 |
| 1:248388023:C:T | donor_gain | 0.6000 |
| 1:248388145:TG:T | acceptor_gain | 0.6000 |
| 1:248388231:T:A | acceptor_gain | 0.6000 |
| 1:248388225:T:TA | acceptor_gain | 0.5900 |
| 1:248388263:ACCAG:A | acceptor_gain | 0.5900 |
| 1:248388310:G:GT | donor_gain | 0.5800 |
| 1:248388479:A:AG | acceptor_gain | 0.5800 |
| 1:248388480:G:GG | acceptor_gain | 0.5800 |
| 1:248388143:TGTG:T | acceptor_gain | 0.5700 |
| 1:248388420:A:G | donor_gain | 0.5600 |
| 1:248388057:T:A | donor_gain | 0.5500 |
| 1:248388143:T:TA | acceptor_gain | 0.5500 |
| 1:248388479:AGTCT:A | acceptor_gain | 0.5500 |
| 1:248388480:GTCTG:G | acceptor_gain | 0.5500 |
| 1:248387904:C:G | donor_gain | 0.5400 |
| 1:248388152:C:G | acceptor_gain | 0.5400 |
| 1:248388280:A:AG | acceptor_gain | 0.5400 |
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1000259636 (1:248376632 T>C,G), RS1000271890 (1:248374032 T>C), RS1000305815 (1:248388677 A>G), RS1000610114 (1:248376810 A>G), RS1000895808 (1:248385390 A>G), RS1000992076 (1:248381270 G>A), RS1001196772 (1:248391048 C>T), RS1001577032 (1:248389990 A>G), RS1001708229 (1:248384863 C>T), RS1001886038 (1:248378276 T>C), RS1002592504 (1:248380593 A>G), RS1002629520 (1:248379182 A>C,G), RS1002774094 (1:248374867 C>T), RS1002953096 (1:248381822 A>G), RS1003088503 (1:248388167 C>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
4 total (human), top 4 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| bisphenol A | increases methylation | 1 |
| Resveratrol | affects cotreatment, decreases expression | 1 |
| Benzo(a)pyrene | affects methylation | 1 |
| Plant Extracts | affects cotreatment, decreases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.