OR5H14

gene
On this page

Summary

OR5H14 (olfactory receptor family 5 subfamily H member 14, HGNC:31286) is a protein-coding gene on chromosome 3q11.2, encoding Olfactory receptor 5H14 (A6NHG9). 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 403273 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 65 total
  • MANE Select transcript: NM_001005514

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:31286
Approved symbolOR5H14
Nameolfactory receptor family 5 subfamily H member 14
Location3q11.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000236032
Ensembl biotypeprotein_coding
Entrez403273

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000437310, ENST00000641380

RefSeq mRNA: 1 — MANE Select: NM_001005514 NM_001005514

CCDS: CCDS33798

Canonical transcript exons

ENST00000641380 — 2 exons

ExonStartEnd
ENSE000038128009814747998147554
ENSE000038139549814936898156614

Expression profiles

Bgee: expression breadth tissue_specific, 4 present calls, max score 44.60.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
placentaUBERON:000198744.60gold quality
hindlimb stylopod muscleUBERON:000425241.66gold quality
sural nerveUBERON:001548839.52gold quality
ganglionic eminenceUBERON:000402338.79gold quality
monocyteCL:000057638.21gold quality
leukocyteCL:000073837.73gold quality
colonic epitheliumUBERON:000039737.20gold quality
bone marrowUBERON:000237137.14gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
apex of heartUBERON:000209834.97gold quality
bloodUBERON:000017834.95gold quality
skeletal muscle tissueUBERON:000113434.75gold quality
muscle tissueUBERON:000238534.19gold quality
granulocyteCL:000009434.14gold quality
calcaneal tendonUBERON:000370133.40gold quality
liverUBERON:000210733.24gold quality
myometriumUBERON:000129632.43gold quality
mucosa of stomachUBERON:000119932.16gold quality
ectocervixUBERON:001224932.12gold quality
descending thoracic aortaUBERON:000234532.08gold quality
superior frontal gyrusUBERON:000266131.98gold quality
uterine cervixUBERON:000000231.88gold quality
popliteal arteryUBERON:000225031.81gold quality
left coronary arteryUBERON:000162631.77gold quality
tibial arteryUBERON:000761031.77gold quality
heart left ventricleUBERON:000208431.43gold quality
urinary bladderUBERON:000125531.32gold quality
cerebellumUBERON:000203731.17gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes4.41
E-GEOD-83139no3.00

Regulation

Is transcription factor: no

Cross-species orthologs

20 orthologs

OrganismSymbolGene ID
mus_musculusOr5h19ENSMUSG00000043357
mus_musculusOr5h18ENSMUSG00000047960
mus_musculusOr5h25ENSMUSG00000060057
mus_musculusOr5h17ENSMUSG00000062105
mus_musculusOr5h22ENSMUSG00000064006
mus_musculusOr5h23ENSMUSG00000094539
mus_musculusOr5h26ENSMUSG00000096695
rattus_norvegicusOr5h18ENSRNOG00000066195
rattus_norvegicusOr5h25bENSRNOG00000071849
rattus_norvegicusOr5h25ENSRNOG00000073369
rattus_norvegicusOr5h17bENSRNOG00000073471
rattus_norvegicusOr5h25dENSRNOG00000073651
rattus_norvegicusOr5h27bENSRNOG00000075854
rattus_norvegicusOr5h26bENSRNOG00000077075
rattus_norvegicusENSRNOG00000077444
rattus_norvegicusOr5h24bENSRNOG00000079937
rattus_norvegicusOr5h17cENSRNOG00000084393
rattus_norvegicusOr5h26ENSRNOG00000085701
rattus_norvegicusOr5h17ENSRNOG00000087735
rattus_norvegicusOr5h24ENSRNOG00000090523

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), OR14C36 (ENSG00000177174), OR6B3 (ENSG00000178586), OR10Q1 (ENSG00000180475), OR8G2P (ENSG00000181214), OR5AK2 (ENSG00000181273), OR5AK3P (ENSG00000181282), OR5M8 (ENSG00000181371), OR8D4 (ENSG00000181518), OR8H1 (ENSG00000181693), OR8K5 (ENSG00000181752), OR8H3 (ENSG00000181761)

Protein

Protein identifiers

Olfactory receptor 5H14A6NHG9 (reviewed: A6NHG9)

All UniProt accessions (1): A6NHG9

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_001005514* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain

Pfam: PF13853

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

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A6NHG9-F189.370.70

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

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

MSigDB gene sets: 17 (showing top): GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, GOBP_DETECTION_OF_STIMULUS, GOBP_SENSORY_PERCEPTION, 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, REACTOME_SENSORY_PERCEPTION, GOBP_DETECTION_OF_CHEMICAL_STIMULUS, GOMF_MOLECULAR_TRANSDUCER_ACTIVITY, chr3q11

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

150 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR5H14ZNF562Q6V9R5506
OR5H14DEFB113Q30KQ7475
OR5H14C5orf63A6NC05448
OR5H14INTS14Q96SY0448
OR5H14SPAG11AQ6PDA7445
OR5H14SWSAP1Q6NVH7431
OR5H14ERI2A8K979419
OR5H14ZNF611Q8N823419
OR5H14RSAD1Q9HA92418
OR5H14ZNF713Q8N859414
OR5H14E7EVR1E7EVR1394
OR5H14ZNF92Q03936370
OR5H14TANGO2Q6ICL3370
OR5H14M9MMK7M9MMK7367
OR5H14PIGZQ86VD9367

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A6NDH6, A6NDL8, A6NET4, A6NHG9, A6NKK0, A6NMS3, P0DN80, P23268, P34982, P35898, Q60887, Q60892, Q7TRF3, Q7TS48, Q8NG80, Q8NG85, Q8NGA0, Q8NGE2, Q8NGF7, Q8NGI8, Q8NGL4, Q8NGS5, Q8NGU1, Q8NGU2, Q8NGV6, Q8NGV7, Q8NGY2, Q8NGY6, Q8NGY9, Q8NH16, Q8NH92, Q8NHB7, Q8NHB8, Q8NHC5, Q8NHC6, Q8NHC7, Q8VEX5, Q8VEX6, Q8VF13, Q8VFB9

Diamond homologs: A6NDH6, A6NET4, A6NHG9, A6NKK0, A6NL26, A6NMS3, O95221, P0C626, P0C628, P0C7N1, P0C7N5, P0DMU2, P0DN80, P34985, P37068, P37070, P37071, P37072, Q13606, Q15617, Q15620, Q60880, Q60882, Q60884, Q60886, Q60893, Q60894, Q6UXT6, Q7TS48, Q8N127, Q8N146, Q8N162, Q8NG75, Q8NG78, Q8NGC0, Q8NGF4, Q8NGF7, Q8NGG0, Q8NGG1, Q8NGG2

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance62
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

224 predictions. Top by Δscore:

VariantEffectΔscore
3:98149645:C:Gdonor_gain0.9800
3:98149649:GA:Gdonor_gain0.9800
3:98149536:A:Tdonor_gain0.9700
3:98149651:G:GGdonor_gain0.9700
3:98149561:T:Gdonor_gain0.9000
3:98149839:G:GAdonor_gain0.8700
3:98149566:T:Gdonor_gain0.8100
3:98149838:T:TAdonor_gain0.8100
3:98149833:G:GGdonor_gain0.7900
3:98149416:GA:Gdonor_gain0.7700
3:98149680:A:Gdonor_gain0.7300
3:98149432:G:GTdonor_gain0.7200
3:98149993:CA:Cacceptor_loss0.7100
3:98149994:A:ACacceptor_loss0.7100
3:98149986:A:AGacceptor_gain0.6900
3:98149418:G:GGdonor_gain0.6700
3:98149417:A:AGdonor_gain0.6600
3:98149455:A:Tdonor_gain0.6400
3:98149995:GGTTC:Gacceptor_gain0.6200
3:98149995:GGTT:Gacceptor_gain0.6100
3:98149648:AGA:Adonor_gain0.5900
3:98149649:GAG:Gdonor_gain0.5900
3:98149987:T:Gacceptor_gain0.5800
3:98149832:T:Gdonor_gain0.5500
3:98149840:G:GGdonor_gain0.5500
3:98150041:T:Gacceptor_gain0.5500
3:98149650:AGT:Adonor_loss0.5400
3:98149651:GT:Gdonor_loss0.5400
3:98149420:T:Adonor_gain0.5300
3:98149652:TAA:Tdonor_loss0.5300

AlphaMissense

2030 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
3:98149887:T:CF168L0.834
3:98149889:C:AF168L0.834
3:98149889:C:GF168L0.834
3:98149419:T:CF12L0.784
3:98149421:T:AF12L0.784
3:98149421:T:GF12L0.784
3:98149914:T:CF177L0.751
3:98149916:T:AF177L0.751
3:98149916:T:GF177L0.751
3:98150256:A:CS291R0.749
3:98150258:C:AS291R0.749
3:98150258:C:GS291R0.749
3:98149750:G:CR122P0.731
3:98149722:T:CF113L0.725
3:98149724:T:AF113L0.725
3:98149724:T:GF113L0.725
3:98149476:T:CF31L0.715
3:98149478:C:AF31L0.715
3:98149478:C:GF31L0.715
3:98150243:T:AN286K0.706
3:98150243:T:GN286K0.706
3:98149739:G:AM118I0.701
3:98149739:G:CM118I0.701
3:98149739:G:TM118I0.701
3:98149741:C:AA119E0.688
3:98150264:A:CR293S0.683
3:98150264:A:TR293S0.683
3:98149762:T:AI126K0.674
3:98149704:A:CS107R0.663
3:98149706:T:AS107R0.663

dbSNP variants (sampled 300 via entrez): RS1000387265 (3:98150268 A>C,G), RS1001202291 (3:98154149 G>T), RS1001283593 (3:98154337 A>G), RS1001401268 (3:98153070 G>A,C), RS1003034914 (3:98147095 C>A), RS1003044745 (3:98146704 G>A,T), RS1003963013 (3:98154292 G>A), RS1005577302 (3:98150468 A>T), RS1005666352 (3:98152911 C>T), RS1005761733 (3:98148347 CTT>C,CT), RS1005963098 (3:98147185 G>C), RS1006000085 (3:98154118 T>G), RS1006040246 (3:98153138 C>A,T), RS1006249652 (3:98148596 C>A,T), RS1006325084 (3:98147467 T>C)

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

1 associations (top):

StudyTraitp-value
GCST005039_1Uncontrolled blood pressure in combination therapy (beta blocker and thiazide diuretic)4.000000e-06

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0007766response to beta blocker

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

6 total (human), top 6 by PubMed support.

ChemicalActions (top 5)PubMed papers
Resveratroldecreases expression, affects cotreatment2
sodium arsenitedecreases expression1
Benzo(a)pyreneincreases methylation1
Copperaffects cotreatment, decreases expression1
Plant Extractsdecreases expression, affects cotreatment1
Valproic Aciddecreases 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.