OR4K13

gene
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Summary

OR4K13 (olfactory receptor family 4 subfamily K member 13, HGNC:15351) is a protein-coding gene on chromosome 14q11.2, encoding Olfactory receptor 4K13 (Q8NH42). 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 390433 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 54 total
  • MANE Select transcript: NM_001004714

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:15351
Approved symbolOR4K13
Nameolfactory receptor family 4 subfamily K member 13
Location14q11.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000176253
Ensembl biotypeprotein_coding
Entrez390433

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000641664, ENST00000641904

RefSeq mRNA: 2 — MANE Select: NM_001004714 NM_001004714, NM_001386029

CCDS: CCDS32028

Canonical transcript exons

ENST00000641904 — 2 exons

ExonStartEnd
ENSE000038123652002939920034981
ENSE000038133042003593820036038

Expression profiles

Bgee: expression breadth not_expressed, 0 present calls, max score 43.24.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
ventricular zoneUBERON:000305343.24gold quality
colonic epitheliumUBERON:000039741.17gold quality
sural nerveUBERON:001548839.89gold quality
bone marrow cellCL:000209239.88gold quality
lower esophagus mucosaUBERON:003583438.01gold quality
ganglionic eminenceUBERON:000402337.13gold quality
cortical plateUBERON:000534336.47gold quality
bone marrowUBERON:000237135.76gold quality
monocyteCL:000057635.49gold quality
leukocyteCL:000073835.26gold quality
granulocyteCL:000009434.44gold quality
mucosa of transverse colonUBERON:000499134.16gold quality
liverUBERON:000210733.81gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
primary visual cortexUBERON:000243632.65gold quality
muscle tissueUBERON:000238532.21gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
adrenal tissueUBERON:001830331.77gold quality
urinary bladderUBERON:000125531.16gold quality
fundus of stomachUBERON:000116030.52gold quality
bloodUBERON:000017830.48gold quality
tonsilUBERON:000237230.10gold quality
prefrontal cortexUBERON:000045129.94gold quality
stromal cell of endometriumCL:000225529.87gold quality
lymph nodeUBERON:000002929.84gold quality
right adrenal gland cortexUBERON:003582729.69gold quality
right lobe of liverUBERON:000111429.61gold quality
superior frontal gyrusUBERON:000266129.42gold quality
pancreasUBERON:000126428.92gold quality
body of pancreasUBERON:000115028.51gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.92

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Paralogs (130): OR1I1 (ENSG00000094661), OR12D3 (ENSG00000112462), OR7A10 (ENSG00000127515), OR7C2 (ENSG00000127529), OR7C1 (ENSG00000127530), OR1E2 (ENSG00000127780), OR1J1 (ENSG00000136834), OR1L4 (ENSG00000136939), OR4D1 (ENSG00000141194), OR4K1 (ENSG00000155249), OR3A3 (ENSG00000159961), OR7G1 (ENSG00000161807), OR1Q1 (ENSG00000165202), OR1K1 (ENSG00000165204), OR4K2 (ENSG00000165762), OR4D6 (ENSG00000166884), OR1F1 (ENSG00000168124), OR4K14 (ENSG00000169484), OR4K15 (ENSG00000169488), OR7G3 (ENSG00000170920), OR7G2 (ENSG00000170923), OR1M1 (ENSG00000170929), OR4D5 (ENSG00000171014), OR1L6 (ENSG00000171459), OR1L3 (ENSG00000171481), OR1L8 (ENSG00000171496), OR1N2 (ENSG00000171501), OR1N1 (ENSG00000171505), OR2AT4 (ENSG00000171561), OR1A1 (ENSG00000172146), OR1A2 (ENSG00000172150), OR4C11 (ENSG00000172188), OR4X2 (ENSG00000172208), OR4D9 (ENSG00000172742), OR10K1 (ENSG00000173285), OR1L1 (ENSG00000173679), OR7D4 (ENSG00000174667), OR4S2 (ENSG00000174982), OR4B1 (ENSG00000175619), OR4D11 (ENSG00000176200)

Protein

Protein identifiers

Olfactory receptor 4K13Q8NH42 (reviewed: Q8NH42)

Alternative names: Olfactory receptor OR14-27

All UniProt accessions (2): A0A126GVS2, Q8NH42

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 (2): NP_001004714, NP_001372958 (=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain
IPR050427Olfactory_ReceptorsFamily

Pfam: PF13853

UniProt features (19 total): topological domain 8, transmembrane region 7, chain 1, glycosylation site 1, disulfide bond 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8NH42-F183.880.45

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 (1): 5

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, ACEVEDO_LIVER_CANCER_WITH_H3K27ME3_DN, 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): 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 (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
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
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

88 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR4K13CCDC91Q7Z6B0477
OR4K13INPP5BP32019391
OR4K13AP1G1O43747371
OR4K13KCNC2Q96PR1348
OR4K13PIP4K2AP48426324
OR4K13KCNQ5Q9NR82311
OR4K13RXFP1Q9HBX9310
OR4K13SPINT1O43278308
OR4K13CMKLR2P46091302
OR4K13POU3F1Q03052290
OR4K13PLCB1Q9NQ66237
OR4K13KCNQ2O43526231
OR4K13ABCB4P21439219
OR4K13PDPRQ8NCN5199
OR4K13CEACAM4O75871196

IntAct

0 interactions, top by confidence:

BioGRID (1): RPL32 (Cross-Linking-MS (XL-MS))

ESM2 similar proteins: A0A096LPK9, A0A0X1KG70, A6NHA9, A6NMZ5, P0C604, P0C623, P0C645, P0DN82, P58180, P58182, Q15615, Q60881, Q6IF82, Q8IXE1, Q8N0Y3, Q8NGA8, Q8NGB4, Q8NGB6, Q8NGC2, Q8NGC3, Q8NGD0, Q8NGD1, Q8NGD2, Q8NGD5, Q8NGE8, Q8NGF4, Q8NGF8, Q8NGF9, Q8NGI4, Q8NGI6, Q8NGJ0, Q8NGJ1, Q8NGL6, Q8NGM1, Q8NGN0, Q8NGN8, Q8NGX5, Q8NH05, Q8NH42, Q8NH49

Diamond homologs: A0A096LPK9, A0A0X1KG70, A6NHA9, A6NMZ5, O60412, O76099, O95013, P0C604, P0C623, P0C645, P0DN82, P23270, P23275, P58173, P58180, P58182, Q15615, Q60878, Q60881, Q60888, Q6IEV9, Q6IEY1, Q6IF82, Q7TQQ0, Q8IXE1, Q8N0Y3, Q8N628, Q8NGA8, Q8NGB2, Q8NGB4, Q8NGB6, Q8NGB8, Q8NGB9, Q8NGC2, Q8NGC3, Q8NGC4, Q8NGC6, Q8NGD0, Q8NGD1, Q8NGD2

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance52
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

278 predictions. Top by Δscore:

VariantEffectΔscore
14:20034492:A:ACdonor_gain0.6800
14:20034493:C:CCdonor_gain0.6800
14:20034614:CAG:Cdonor_gain0.6700
14:20034616:G:Cdonor_gain0.6300
14:20034493:CGTT:Cdonor_gain0.6100
14:20034207:C:CTacceptor_gain0.5900
14:20034727:T:TAdonor_gain0.5900
14:20034190:T:Cacceptor_gain0.5500
14:20034734:C:CTdonor_gain0.5400
14:20034583:A:Cdonor_gain0.5300
14:20034210:A:Tacceptor_gain0.5000
14:20034754:T:Adonor_gain0.4900
14:20034251:C:CTacceptor_gain0.4800
14:20034085:A:ACdonor_gain0.4700
14:20034086:C:CCdonor_gain0.4700
14:20034189:CT:Cacceptor_gain0.4700
14:20034190:TT:Tacceptor_gain0.4700
14:20034431:TCCCA:Tdonor_gain0.4700
14:20034432:CCCAC:Cdonor_gain0.4700
14:20034433:CCACC:Cdonor_gain0.4700
14:20034434:CACCC:Cdonor_gain0.4700
14:20034435:ACCCA:Adonor_gain0.4700
14:20034436:CCCAG:Cdonor_gain0.4700
14:20034734:CCA:Cdonor_gain0.4700
14:20034081:CCTAA:Cdonor_gain0.4600
14:20034471:TCCCC:Tdonor_gain0.4500
14:20034621:CAAGA:Cdonor_gain0.4500
14:20033985:G:Cacceptor_gain0.4400
14:20034086:C:Aacceptor_gain0.4400
14:20034735:C:CTdonor_gain0.4400

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000031384 (14:20035081 G>A), RS1000490138 (14:20036391 C>T), RS1001180230 (14:20034548 T>C), RS1001342959 (14:20031821 T>A,C), RS1001729033 (14:20029061 A>C,G), RS1002334082 (14:20033319 G>C), RS1002404588 (14:20037988 T>C), RS1003128895 (14:20029025 C>A,T), RS1003147838 (14:20032399 A>G,T), RS1003180464 (14:20031989 G>A), RS1003813434 (14:20037081 A>G), RS1004138513 (14:20030129 G>A,T), RS1005101700 (14:20031701 T>G), RS1005152278 (14:20031417 G>A), RS1005729713 (14:20037970 G>A)

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
Benzo(a)pyreneincreases expression, decreases methylation2
bisphenol Aincreases methylation, affects cotreatment1
Fulvestrantaffects cotreatment, increases 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.