OR10AG1

gene
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Summary

OR10AG1 (olfactory receptor family 10 subfamily AG member 1, HGNC:19607) is a protein-coding gene on chromosome 11q12.1, encoding Olfactory receptor 10AG1 (Q8NH19). 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 282770 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 36 total
  • MANE Select transcript: NM_001005491

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:19607
Approved symbolOR10AG1
Nameolfactory receptor family 10 subfamily AG member 1
Location11q12.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000174970
Ensembl biotypeprotein_coding
Entrez282770

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000312345, ENST00000641071

RefSeq mRNA: 1 — MANE Select: NM_001005491 NM_001005491

CCDS: CCDS31514

Canonical transcript exons

ENST00000641071 — 2 exons

ExonStartEnd
ENSE000038135085596575555968507
ENSE000038139395596989255969945

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:001548835.00gold quality
monocyteCL:000057634.25silver quality
leukocyteCL:000073833.65silver 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:000045129.04gold quality
liverUBERON:000210728.65gold quality
duodenumUBERON:000211428.14gold quality
urinary bladderUBERON:000125527.94gold quality
lymph nodeUBERON:000002927.57gold quality
olfactory segment of nasal mucosaUBERON:000538627.36gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.55gold quality
vermiform appendixUBERON:000115426.42gold quality
bloodUBERON:000017826.32gold quality
gall bladderUBERON:000211025.98gold quality
placentaUBERON:000198725.81gold quality
muscle of legUBERON:000138324.86gold quality
primary visual cortexUBERON:000243624.61gold quality
pancreasUBERON:000126424.26gold quality
superior frontal gyrusUBERON:000266124.08gold quality
frontal cortexUBERON:000187024.01gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ENAD-17no130.00
E-ANND-3no2.30

Regulation

Is transcription factor: no

Cross-species orthologs

9 orthologs

OrganismSymbolGene ID
mus_musculusOr10ag2ENSMUSG00000043274
mus_musculusOr10ag57ENSMUSG00000047594
mus_musculusOr10ag54ENSMUSG00000070855
mus_musculusOr10ag56ENSMUSG00000083706
mus_musculusOr10ag55ENSMUSG00000089732
rattus_norvegicusOr10ag57ENSRNOG00000037837
rattus_norvegicusOr10ag54ENSRNOG00000066294
rattus_norvegicusOr10ag54bENSRNOG00000066948
rattus_norvegicusENSRNOG00000089112

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), 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), OR2T10 (ENSG00000184022)

Protein

Protein identifiers

Olfactory receptor 10AG1Q8NH19 (reviewed: Q8NH19)

Alternative names: Olfactory receptor OR11-160

All UniProt accessions (3): Q8NH19, A0A126GVM8, A0A2U3TZR9

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_001005491* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain

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-Q8NH19-F191.380.74

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): 88–180

Glycosylation sites (1): 82

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

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

MSigDB gene sets: 16 (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, REACTOME_OLFACTORY_SIGNALING_PATHWAY, REACTOME_SENSORY_PERCEPTION, GOBP_DETECTION_OF_CHEMICAL_STIMULUS, GOMF_MOLECULAR_TRANSDUCER_ACTIVITY, chr11q12

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 (3): G protein-coupled receptor activity (GO:0004930), olfactory receptor activity (GO:0004984), protein binding (GO:0005515)

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
binding1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

226 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR10AG1TSGA10IPQ3SY00601
OR10AG1ABCC12Q96J65551
OR10AG1PIGZQ86VD9432
OR10AG1AK9Q5TCS8400
OR10AG1NPAP1Q9NZP6376
OR10AG1PLBD1Q6P4A8348
OR10AG1MMABQ96EY8348
OR10AG1SLX4Q8IY92347
OR10AG1DEGS2Q6QHC5315
OR10AG1EPCIPQ9NYP8312
OR10AG1FXYD3Q14802304
OR10AG1IQGAP3Q86VI3299
OR10AG1KIF26BQ2KJY2296
OR10AG1ZNF420Q8TAQ5291
OR10AG1FAM149B1Q96BN6290

IntAct

16 interactions, top by confidence:

ABTypeScore
OR10AG1CREB3L1psi-mi:“MI:0915”(physical association)0.560
AQP2OR10AG1psi-mi:“MI:0915”(physical association)0.560
FFAR2OR10AG1psi-mi:“MI:0915”(physical association)0.560
MUC1OR10AG1psi-mi:“MI:0915”(physical association)0.560
EBAG9OR10AG1psi-mi:“MI:0915”(physical association)0.560
OR10AG1CREB3L1psi-mi:“MI:0915”(physical association)0.000
OR10AG1AQP2psi-mi:“MI:0915”(physical association)0.000
OR10AG1MUC1psi-mi:“MI:0915”(physical association)0.000
OR10AG1FFAR2psi-mi:“MI:0915”(physical association)0.000
OR10AG1EBAG9psi-mi:“MI:0915”(physical association)0.000

BioGRID (5): OR10AG1 (Two-hybrid), OR10AG1 (Two-hybrid), OR10AG1 (Two-hybrid), OR10AG1 (Two-hybrid), MUC1 (Two-hybrid)

ESM2 similar proteins: A6NF89, A6NJZ3, O76000, O95007, P0C626, P0C628, P23269, P23273, P34986, P37067, P37069, P37070, P37071, P58181, Q13606, Q60884, Q60895, Q8N162, Q8NG80, Q8NGC8, Q8NGE1, Q8NGE2, Q8NGG4, Q8NGQ6, Q8NGS4, Q8NGT1, Q8NGV7, Q8NGZ3, Q8NGZ9, Q8NH19, Q8NH51, Q8VEW5, Q8VEW6, Q8VEX5, Q8VEZ0, Q8VF66, Q8VF76, Q8VFB9, Q8VFD0, Q8VFK2

Diamond homologs: A4D2G3, A6ND48, A6NL26, O43749, O60412, O76099, P0C7N5, P0DMU2, P0DN82, P23265, P23266, P23269, P23272, P23273, P23274, P30953, P30955, P34984, P34985, P34986, P35896, P47887, P47890, P58173, P58181, P58182, P70526, Q0VAX9, Q13606, Q13607, Q15617, Q15619, Q60893, Q6IFN5, Q6UXT6, Q7TQQ0, Q7TRF3, Q8N127, Q8NG98, Q8NGA6

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance30
Likely benign3
Benign3

Top pathogenic / likely-pathogenic (0)

SpliceAI

280 predictions. Top by Δscore:

VariantEffectΔscore
11:55967955:C:CTacceptor_gain0.7800
11:55967953:C:CTacceptor_gain0.7200
11:55968408:A:ACdonor_gain0.7200
11:55968408:AAAAG:Adonor_gain0.7200
11:55967836:C:CTacceptor_gain0.6900
11:55968409:A:Cdonor_gain0.6900
11:55968393:A:Cdonor_gain0.6800
11:55967837:A:Cacceptor_gain0.6700
11:55967813:CAAAA:Cacceptor_gain0.6500
11:55968221:T:Adonor_gain0.6400
11:55967949:A:Cacceptor_gain0.6200
11:55968169:C:CTacceptor_gain0.6200
11:55968170:A:Tacceptor_gain0.6000
11:55968459:T:TAdonor_gain0.6000
11:55968404:A:ACdonor_gain0.5900
11:55968405:C:CCdonor_gain0.5900
11:55967902:T:Cdonor_gain0.5800
11:55968169:C:Tacceptor_gain0.5800
11:55967836:C:Tacceptor_gain0.5700
11:55968110:A:ACdonor_gain0.5600
11:55968111:C:CCdonor_gain0.5600
11:55967734:C:CTacceptor_gain0.5500
11:55967735:A:Tacceptor_gain0.5500
11:55968025:C:CTdonor_gain0.5500
11:55968026:T:TTdonor_gain0.5500
11:55968125:G:Cdonor_gain0.5500
11:55968174:A:Cacceptor_gain0.5400
11:55967723:AGTAC:Aacceptor_loss0.5300
11:55967725:TACC:Tacceptor_loss0.5300
11:55967726:ACCT:Aacceptor_loss0.5300

AlphaMissense

2124 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:55968455:A:CF3L0.895
11:55968455:A:TF3L0.895
11:55968457:A:GF3L0.895
11:55967987:A:CF159L0.828
11:55967987:A:TF159L0.828
11:55967989:A:GF159L0.828
11:55968440:A:CF8L0.824
11:55968440:A:TF8L0.824
11:55968442:A:GF8L0.824
11:55968126:C:GR113P0.822
11:55968137:C:AM109I0.787
11:55968137:C:GM109I0.787
11:55968137:C:TM109I0.787
11:55967738:G:CF242L0.780
11:55967738:G:TF242L0.780
11:55967740:A:GF242L0.780
11:55967999:G:CF155L0.772
11:55967999:G:TF155L0.772
11:55968001:A:GF155L0.772
11:55967960:G:CF168L0.768
11:55967960:G:TF168L0.768
11:55967962:A:GF168L0.768
11:55968046:A:GW140R0.767
11:55968046:A:TW140R0.767
11:55967735:A:CF243L0.760
11:55967735:A:TF243L0.760
11:55967737:A:GF243L0.760
11:55967777:G:CF229L0.746
11:55967777:G:TF229L0.746
11:55967779:A:GF229L0.746

dbSNP variants (sampled 300 via entrez): RS1000131384 (11:55968862 T>C), RS1000903424 (11:55969073 A>G), RS1000935165 (11:55968972 C>A), RS1001640466 (11:55966052 ATTATC>A), RS1001880008 (11:55968198 G>A), RS1001932121 (11:55968535 T>C), RS1002592960 (11:55967569 A>G), RS1002601571 (11:55966169 C>T), RS1002827204 (11:55971257 C>T), RS1002957034 (11:55971464 G>A,T), RS1003323246 (11:55967559 C>T), RS1004344366 (11:55970821 C>T), RS1004829178 (11:55966919 C>T), RS1004890157 (11:55965771 C>T), RS1005569536 (11:55969387 A>T)

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

1 total (human), top 1 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyrenedecreases 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.