OR13J1

gene
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Summary

OR13J1 (olfactory receptor family 13 subfamily J member 1, HGNC:15108) is a protein-coding gene on chromosome 9p13.3, encoding Olfactory receptor 13J1 (Q8NGT2). 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 392309 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 62 total
  • MANE Select transcript: NM_001004487

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:15108
Approved symbolOR13J1
Nameolfactory receptor family 13 subfamily J member 1
Location9p13.3
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000168828
Ensembl biotypeprotein_coding
Entrez392309

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000377981

RefSeq mRNA: 1 — MANE Select: NM_001004487 NM_001004487

CCDS: CCDS35011

Canonical transcript exons

ENST00000377981 — 1 exons

ExonStartEnd
ENSE000014757463586946335870401

Expression profiles

Bgee: expression breadth broad, 51 present calls, max score 53.83.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
prefrontal cortexUBERON:000045153.83gold quality
sural nerveUBERON:001548853.81gold quality
primary visual cortexUBERON:000243653.17gold quality
frontal cortexUBERON:000187052.54gold quality
anterior cingulate cortexUBERON:000983551.78gold quality
cerebral cortexUBERON:000095651.48gold quality
Ammon’s hornUBERON:000195451.38gold quality
right frontal lobeUBERON:000281051.19gold quality
superior frontal gyrusUBERON:000266151.08gold quality
putamenUBERON:000187450.56gold quality
dorsolateral prefrontal cortexUBERON:000983450.55gold quality
temporal lobeUBERON:000187150.20gold quality
amygdalaUBERON:000187649.92gold quality
Brodmann (1909) area 9UBERON:001354049.84gold quality
caudate nucleusUBERON:000187349.27gold quality
cortical plateUBERON:000534349.27gold quality
nucleus accumbensUBERON:000188249.03gold quality
brainUBERON:000095548.10gold quality
skeletal muscle tissueUBERON:000113447.35silver quality
hindlimb stylopod muscleUBERON:000425247.31silver quality
hypothalamusUBERON:000189846.16gold quality
C1 segment of cervical spinal cordUBERON:000646945.85gold quality
cerebellumUBERON:000203744.43gold quality
cerebellar cortexUBERON:000212944.16gold quality
cerebellar hemisphereUBERON:000224544.07gold quality
substantia nigraUBERON:000203843.63gold quality
right hemisphere of cerebellumUBERON:001489043.54gold quality
lower esophagus muscularis layerUBERON:003583342.87gold quality
lower esophagusUBERON:001347342.75gold quality
muscle tissueUBERON:000238542.61silver quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.99

Regulation

Is transcription factor: no

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusOr13j1ENSMUSG00000046450
rattus_norvegicusOr13j1ENSRNOG00000082595

Paralogs (92): OR2B6 (ENSG00000124657), OR13C9 (ENSG00000136839), OR13C4 (ENSG00000148136), OR2M5 (ENSG00000162727), OR10A5 (ENSG00000166363), OR2D2 (ENSG00000166368), OR2B2 (ENSG00000168131), OR2C1 (ENSG00000168158), 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), OR2T10 (ENSG00000184022)

Protein

Protein identifiers

Olfactory receptor 13J1Q8NGT2 (reviewed: Q8NGT2)

Alternative names: Olfactory receptor OR9-2

All UniProt accessions (1): Q8NGT2

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_001004487* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain

Pfam: PF13853

UniProt features (20 total): topological domain 8, transmembrane region 7, glycosylation site 2, chain 1, disulfide bond 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8NGT2-F182.070.33

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): 97–189

Glycosylation sites (2): 5, 191

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

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

MSigDB gene sets: 28 (showing top): GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, chr9p13, 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, GSE17721_CTRL_VS_CPG_0.5H_BMDC_UP, GSE17721_LPS_VS_POLYIC_6H_BMDC_UP, GSE17721_POLYIC_VS_CPG_0.5H_BMDC_UP, GSE17721_LPS_VS_CPG_0.5H_BMDC_DN

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

156 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR13J1KRTAP19-7Q3SYF9581
OR13J1FAM181AQ8N9Y4506
OR13J1SYNGR4O95473468
OR13J1ZNF781Q8N8C0435
OR13J1FTHL17Q9BXU8417
OR13J1PCDHGB4Q9UN71417
OR13J1STON1Q9Y6Q2400
OR13J1PHETA1Q8N4B1398
OR13J1EFR3AQ14156380
OR13J1KRT84Q9NSB2375
OR13J1UNC79Q9P2D8372
OR13J1NMBRP28336372
OR13J1KIF25Q9UIL4370
OR13J1ADGRF4Q8IZF3369
OR13J1MTFR2Q6P444366

IntAct

2 interactions, top by confidence:

ABTypeScore
OR13J1FZD7psi-mi:“MI:0914”(association)0.350

BioGRID (8): CCPG1 (Affinity Capture-MS), FZD7 (Affinity Capture-MS), MOSPD2 (Affinity Capture-MS), GOLGA5 (Affinity Capture-MS), ATP2B3 (Affinity Capture-MS), SLC41A3 (Affinity Capture-MS), SARAF (Affinity Capture-MS), HMGCR (Affinity Capture-MS)

ESM2 similar proteins: A6ND48, A6NFC9, B2RN74, O43869, O60412, O60431, P23265, P31388, P34987, P47883, P47884, P47887, P58170, Q0VAX9, Q5JRS4, Q60894, Q6IFN5, Q7Z3T1, Q8NG78, Q8NG84, Q8NG94, Q8NG99, Q8NGC0, Q8NGC1, Q8NGC5, Q8NGE7, Q8NGG2, Q8NGG3, Q8NGN1, Q8NGN2, Q8NGR1, Q8NGR2, Q8NGR6, Q8NGT2, Q8NGW1, Q8NGW6, Q8NGZ2, Q8NGZ5, Q8NH06, Q8NH07

Diamond homologs: A4D2G3, O43749, O60403, O60404, O76099, P0C629, P0DN81, P23270, P30953, P30954, P34984, P34986, P58173, P58181, P70526, Q13606, Q5JRS4, Q60880, Q60890, Q62007, Q6IF99, Q6IFH4, Q6UXT6, Q7TR96, Q8N127, Q8NG75, Q8NGA5, Q8NGA6, Q8NGC0, Q8NGC3, Q8NGC5, Q8NGE3, Q8NGE5, Q8NGF4, Q8NGG3, Q8NGI7, Q8NGI9, Q8NGJ0, Q8NGN3, Q8NGN4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance55
Likely benign7
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

58 predictions. Top by Δscore:

VariantEffectΔscore
9:35869495:T:Adonor_gain0.6200
9:35869515:T:TAdonor_gain0.5900
9:35869820:G:Tdonor_gain0.5300
9:35869909:T:TAacceptor_gain0.5200
9:35869880:G:Tdonor_gain0.5100
9:35869510:TC:Tdonor_gain0.4900
9:35869827:G:Cdonor_gain0.4900
9:35869605:T:TAdonor_gain0.4700
9:35869506:T:TAdonor_gain0.4600
9:35869610:A:ACdonor_gain0.4600
9:35869611:C:CCdonor_gain0.4600
9:35869611:CT:Cdonor_gain0.4300
9:35869823:CGACG:Cdonor_gain0.4300
9:35869660:C:CTdonor_gain0.4200
9:35869661:T:TTdonor_gain0.4200
9:35869699:A:ACdonor_gain0.4100
9:35869579:TGAAG:Tdonor_gain0.4000
9:35869910:C:Aacceptor_gain0.3900
9:35869505:CTCCT:Cdonor_gain0.3800
9:35869506:TCCTT:Tdonor_gain0.3800
9:35869507:CCTTC:Cdonor_gain0.3800
9:35869629:A:Cdonor_gain0.3800
9:35869698:CA:Cdonor_gain0.3800
9:35869606:C:Adonor_gain0.3500
9:35869701:C:Tdonor_gain0.3500
9:35869929:G:Cdonor_gain0.3500
9:35869508:CT:Cdonor_gain0.3400
9:35869509:TTC:Tdonor_gain0.3400
9:35869824:G:Tdonor_gain0.3100
9:35869934:CGACT:Cacceptor_gain0.3000

AlphaMissense

2008 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
9:35870366:G:CF12L0.837
9:35870366:G:TF12L0.837
9:35870368:A:GF12L0.837
9:35869871:G:CF177L0.735
9:35869871:G:TF177L0.735
9:35869873:A:GF177L0.735
9:35869898:G:CF168L0.705
9:35869898:G:TF168L0.705
9:35869900:A:GF168L0.705
9:35870351:A:CF17L0.704
9:35870351:A:TF17L0.704
9:35870353:A:GF17L0.704
9:35870120:A:CF94L0.703
9:35870120:A:TF94L0.703
9:35870122:A:GF94L0.703
9:35869649:G:CF251L0.665
9:35869649:G:TF251L0.665
9:35869651:A:GF251L0.665
9:35870171:A:CF77L0.640
9:35870171:A:TF77L0.640
9:35870173:A:GF77L0.640
9:35870318:G:CF28L0.617
9:35870318:G:TF28L0.617
9:35870320:A:GF28L0.617
9:35869688:G:CF238L0.614
9:35869688:G:TF238L0.614
9:35869690:A:GF238L0.614
9:35870219:G:CF61L0.573
9:35870219:G:TF61L0.573
9:35870221:A:GF61L0.573

dbSNP variants (sampled 300 via entrez): RS1000097909 (9:35869171 C>G), RS1001883133 (9:35872015 A>C), RS1002813887 (9:35871781 G>T), RS1002990280 (9:35871087 C>G), RS1004991538 (9:35869159 A>T), RS1005619749 (9:35872238 C>G), RS1006290910 (9:35872314 A>C,G), RS1008291873 (9:35869037 G>A), RS1009637855 (9:35872049 T>C), RS1011415159 (9:35871416 A>T), RS1011528759 (9:35870971 G>A,C), RS1011736967 (9:35871131 A>G), RS1012526917 (9:35869523 C>T), RS1012907826 (9:35870752 A>G), RS1013458570 (9:35870469 G>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

3 total (human), top 3 by PubMed support.

ChemicalActions (top 5)PubMed papers
Resveratrolaffects cotreatment, decreases expression1
Benzo(a)pyreneaffects methylation, increases methylation1
Plant Extractsdecreases expression, affects cotreatment1

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.