OR14C36

gene
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Summary

OR14C36 (olfactory receptor family 14 subfamily C member 36, HGNC:15026) is a protein-coding gene on chromosome 1q44, encoding Olfactory receptor 14C36 (Q8NHC7). 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 127066 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 44 total
  • MANE Select transcript: NM_001001918

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:15026
Approved symbolOR14C36
Nameolfactory receptor family 14 subfamily C member 36
Location1q44
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000177174
Ensembl biotypeprotein_coding
Entrez127066

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000317861

RefSeq mRNA: 1 — MANE Select: NM_001001918 NM_001001918

CCDS: CCDS31112

Canonical transcript exons

ENST00000317861 — 1 exons

ExonStartEnd
ENSE00001277275248348775248349713

Expression profiles

Bgee: expression breadth tissue_specific, 3 present calls, max score 37.20.

Top tissues by expression

125 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
skeletal muscle tissueUBERON:000113433.38gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
bone marrowUBERON:000237131.74gold quality
muscle tissueUBERON:000238531.06gold quality
right uterine tubeUBERON:000130231.03gold quality
sural nerveUBERON:001548830.93gold quality
stromal cell of endometriumCL:000225529.87gold quality
prefrontal cortexUBERON:000045129.23gold quality
liverUBERON:000210728.61gold quality
monocyteCL:000057628.43gold quality
leukocyteCL:000073828.35gold quality
duodenumUBERON:000211428.14gold quality
primary visual cortexUBERON:000243627.80gold quality
lymph nodeUBERON:000002927.57gold quality
tonsilUBERON:000237227.05gold quality
urinary bladderUBERON:000125526.89gold quality
islet of LangerhansUBERON:000000626.55gold quality
Brodmann (1909) area 9UBERON:001354026.44gold quality
vermiform appendixUBERON:000115426.42gold quality
bloodUBERON:000017826.25gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
frontal cortexUBERON:000187025.64gold quality
muscle of legUBERON:000138324.87gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.65

Regulation

Is transcription factor: no

Cross-species orthologs

14 orthologs

OrganismSymbolGene ID
mus_musculusOr14c43ENSMUSG00000020168
mus_musculusOr14c45ENSMUSG00000057067
mus_musculusOr14c46ENSMUSG00000057540
mus_musculusOr14c41ENSMUSG00000059319
mus_musculusOr14c39ENSMUSG00000060688
mus_musculusOr14c44ENSMUSG00000061549
mus_musculusOr14c40ENSMUSG00000063394
mus_musculusOr14c42ENSMUSG00000092372
mus_musculusOr14n1ENSMUSG00000092401
rattus_norvegicusOr14c39bENSRNOG00000029233
rattus_norvegicusOr14n1ENSRNOG00000076037
rattus_norvegicusOr14c40ENSRNOG00000081552
rattus_norvegicusOr14c43ENSRNOG00000084504
rattus_norvegicusOr14c39ENSRNOG00000090780

Paralogs (96): OR5C1 (ENSG00000148215), OR5F1 (ENSG00000149133), OR8K1 (ENSG00000150261), OR5M9 (ENSG00000150269), OR14K1 (ENSG00000153230), OR8J3 (ENSG00000167822), OR5I1 (ENSG00000167825), OR5AU1 (ENSG00000169327), OR9K2 (ENSG00000170605), OR8B12 (ENSG00000170953), OR10H3 (ENSG00000171936), OR8I2 (ENSG00000172154), OR8U1 (ENSG00000172199), OR10V1 (ENSG00000172289), OR5A1 (ENSG00000172320), OR5A2 (ENSG00000172324), OR5B12 (ENSG00000172362), OR5B2 (ENSG00000172365), OR9I1 (ENSG00000172377), OR9G4 (ENSG00000172457), OR5AR1 (ENSG00000172459), OR5AP2 (ENSG00000172464), OR8J1 (ENSG00000172487), OR5B3 (ENSG00000172769), OR10W1 (ENSG00000172772), OR5M3 (ENSG00000174937), OR5J2 (ENSG00000174957), OR10H4 (ENSG00000176231), OR5AN1 (ENSG00000176495), OR6B3 (ENSG00000178586), OR10Q1 (ENSG00000180475), OR8G2P (ENSG00000181214), OR5AK2 (ENSG00000181273), OR5AK3P (ENSG00000181282), OR5M8 (ENSG00000181371), OR8D4 (ENSG00000181518), OR8H1 (ENSG00000181693), OR8K5 (ENSG00000181752), OR8H3 (ENSG00000181761), OR8H2 (ENSG00000181767)

Protein

Protein identifiers

Olfactory receptor 14C36Q8NHC7 (reviewed: Q8NHC7)

Alternative names: Olfactory receptor 5BF1, Olfactory receptor OR1-59

All UniProt accessions (1): Q8NHC7

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_001001918* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain
IPR050516Olfactory_GPCRFamily

Pfam: PF13853

UniProt features (21 total): topological domain 8, transmembrane region 7, sequence variant 3, chain 1, glycosylation site 1, disulfide bond 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8NHC7-F186.830.49

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): 95–187

Glycosylation sites (1): 3

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

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

MSigDB gene sets: 19 (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_ODORANT_BINDING, 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, MATSUMIYA_PBMC_MODIFIED_VACCINIA_ANKARA_VACCINE_AGE_18_55YO_VACCINATED_VS_CONTROL_TREATED_IN_VITRO_WITH_WILD_TYPE_MVA_6HR_UP, REACTOME_SENSORY_PERCEPTION

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 (3): G protein-coupled receptor activity (GO:0004930), olfactory receptor activity (GO:0004984), odorant binding (GO:0005549)

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
binding1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

130 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR14C36LENG1Q96BZ8476
OR14C36RFX8Q6ZV50416
OR14C36SLC16A13Q7RTY0328
OR14C36KCNRGQ8N5I3321
OR14C36CBLN4Q9NTU7303
OR14C36DOCK11Q5JSL3271
OR14C36DOCK6Q96HP0261
OR14C36ZMYM3Q14202259
OR14C36DOCK10Q96BY6259
OR14C36DOCK9Q9BZ29257
OR14C36COL7A1Q02388246
OR14C36DOCK3Q8IZD9244
OR14C36DNAH11Q96DT5235
OR14C36PRKCSHP14314226
OR14C36ELP3Q9H9T3225

IntAct

2 interactions, top by confidence:

ABTypeScore
OR14C36HSPD1psi-mi:“MI:0915”(physical association)0.400

BioGRID (2): OR14C36 (Proximity Label-MS), OR14C36 (Cross-Linking-MS (XL-MS))

ESM2 similar proteins: A0A2R8YED5, A6ND48, B2RN74, O60412, O76099, O76100, O95047, P23271, P23272, P34982, P37069, P37072, P47884, P47890, P58170, Q15622, Q60879, Q8NG84, Q8NG94, Q8NG95, Q8NG98, Q8NG99, Q8NGA0, Q8NGA2, Q8NGE0, Q8NGG1, Q8NGL0, Q8NGP2, Q8NGS2, Q8NGW1, Q8NGZ2, Q8NGZ5, Q8NH06, Q8NH07, Q8NH80, Q8NHA4, Q8NHC7, Q8VEY3, Q8VFC9, Q8WZA6

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

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance42
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

483 predictions. Top by Δscore:

VariantEffectΔscore
1:248348960:G:GTdonor_gain0.7900
1:248349055:G:GTdonor_gain0.7000
1:248349440:C:Aacceptor_gain0.7000
1:248349639:A:AGacceptor_gain0.7000
1:248349640:G:GGacceptor_gain0.7000
1:248349436:C:CAacceptor_gain0.6900
1:248349640:GTCTT:Gacceptor_gain0.6800
1:248348961:A:Tdonor_gain0.6700
1:248349457:G:Cacceptor_gain0.6700
1:248349442:T:TAacceptor_gain0.6600
1:248349447:G:Aacceptor_gain0.6500
1:248349665:G:GAdonor_gain0.6500
1:248349579:GATC:Gdonor_gain0.6400
1:248349446:C:Aacceptor_gain0.6300
1:248349512:GTC:Gdonor_gain0.6300
1:248349222:G:GAdonor_gain0.6200
1:248349379:TGGGG:Tacceptor_gain0.6200
1:248349380:GGGGG:Gacceptor_gain0.6200
1:248349055:G:Tdonor_gain0.6100
1:248349664:T:TAdonor_gain0.6000
1:248349080:G:GAdonor_gain0.5900
1:248349640:GT:Gacceptor_gain0.5900
1:248349279:TCC:Tdonor_gain0.5700
1:248349599:T:Gdonor_gain0.5700
1:248348881:C:Gdonor_gain0.5600
1:248349323:G:GTdonor_gain0.5600
1:248349456:A:Gacceptor_gain0.5600
1:248349638:CAG:Cacceptor_gain0.5600
1:248349052:C:Tdonor_gain0.5500
1:248349071:C:Adonor_gain0.5500

AlphaMissense

2054 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
1:248348802:T:CF10L0.926
1:248348804:T:AF10L0.926
1:248348804:T:GF10L0.926
1:248349258:T:CF162L0.862
1:248349260:C:AF162L0.862
1:248349260:C:GF162L0.862
1:248349300:T:CF176L0.839
1:248349302:C:AF176L0.839
1:248349302:C:GF176L0.839
1:248349519:T:CF249L0.837
1:248349521:C:AF249L0.837
1:248349521:C:GF249L0.837
1:248349297:T:CF175L0.830
1:248349299:C:AF175L0.830
1:248349299:C:GF175L0.830
1:248349270:T:CF166L0.818
1:248349272:C:AF166L0.818
1:248349272:C:GF166L0.818
1:248348817:T:CF15L0.805
1:248348819:T:AF15L0.805
1:248348819:T:GF15L0.805
1:248349072:T:CF100L0.787
1:248349074:C:AF100L0.787
1:248349074:C:GF100L0.787
1:248349639:A:CS289R0.785
1:248349641:T:AS289R0.785
1:248349641:T:GS289R0.785
1:248349219:A:CS149R0.767
1:248349221:T:AS149R0.767
1:248349221:T:GS149R0.767

dbSNP variants (sampled 300 via entrez): RS1000121666 (1:248348663 A>G), RS1001744973 (1:248349726 G>A,C), RS1005517285 (1:248349472 C>A,G), RS1005852782 (1:248347987 C>T), RS1007659917 (1:248347940 A>G), RS1008989469 (1:248349054 G>A), RS1011708785 (1:248347320 T>C), RS1012637004 (1:248347024 A>G), RS1013898600 (1:248348283 C>A), RS1014590686 (1:248347993 A>C), RS1016936105 (1:248349478 C>A,G), RS1018544688 (1:248349576 C>T), RS1019700534 (1:248350170 G>A), RS1020509577 (1:248347034 G>T), RS1021017373 (1:248348423 C>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
CGP 52608increases reaction, affects binding1
Benzo(a)pyrenedecreases methylation1
Aflatoxin B1decreases methylation1

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.