OR10H2

gene
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Summary

OR10H2 (olfactory receptor family 10 subfamily H member 2, HGNC:8173) is a protein-coding gene on chromosome 19p13.12, encoding Olfactory receptor 10H2 (O60403). 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 26538 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 71 total
  • MANE Select transcript: NM_013939

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:8173
Approved symbolOR10H2
Nameolfactory receptor family 10 subfamily H member 2
Location19p13.12
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000171942
Ensembl biotypeprotein_coding
Entrez26538

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000305899

RefSeq mRNA: 1 — MANE Select: NM_013939 NM_013939

CCDS: CCDS12333

Canonical transcript exons

ENST00000305899 — 1 exons

ExonStartEnd
ENSE000011326451572802415729052

Expression profiles

Bgee: expression breadth not_expressed, 0 present calls, max score 42.09.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
colonic epitheliumUBERON:000039742.09gold quality
bone marrow cellCL:000209238.58gold quality
granulocyteCL:000009437.15gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113434.99gold quality
muscle tissueUBERON:000238533.46gold quality
bone marrowUBERON:000237132.98gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
sural nerveUBERON:001548830.93gold quality
stromal cell of endometriumCL:000225529.87gold quality
prefrontal cortexUBERON:000045129.38gold quality
tonsilUBERON:000237228.80gold quality
leukocyteCL:000073828.62gold quality
duodenumUBERON:000211428.14gold quality
monocyteCL:000057628.09gold quality
smooth muscle tissueUBERON:000113527.94gold quality
placentaUBERON:000198727.65gold quality
lymph nodeUBERON:000002927.57gold quality
superior frontal gyrusUBERON:000266127.12gold quality
vermiform appendixUBERON:000115426.42gold quality
bloodUBERON:000017826.40gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
muscle of legUBERON:000138325.14gold quality
primary visual cortexUBERON:000243624.61gold quality
skin of abdomenUBERON:000141624.47gold quality
frontal cortexUBERON:000187024.16gold quality
uterine cervixUBERON:000000224.06gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.98

Regulation

Is transcription factor: no

Cross-species orthologs

8 orthologs

OrganismSymbolGene ID
mus_musculusOr10h1ENSMUSG00000093884
mus_musculusOr10h1bENSMUSG00000094891
mus_musculusOr10h5ENSMUSG00000096169
rattus_norvegicusOlr1092ENSRNOG00000073810
rattus_norvegicusOr10h1ENSRNOG00000074063
rattus_norvegicusOlr1090ENSRNOG00000082788
rattus_norvegicusOlr1093ENSRNOG00000090741
rattus_norvegicusOr10h1dENSRNOG00000091234

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), 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 10H2O60403 (reviewed: O60403)

Alternative names: Olfactory receptor OR19-23

All UniProt accessions (2): O60403, A0A126GWJ7

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_039227* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain

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-O60403-F188.120.66

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

2 pathways

IDPathway
R-HSA-381753Olfactory Signaling Pathway
R-HSA-9752946Expression and translocation of olfactory receptors

MSigDB gene sets: 28 (showing top): GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, JAZAG_TGFB1_SIGNALING_VIA_SMAD4_UP, KEGG_OLFACTORY_TRANSDUCTION, GOBP_DETECTION_OF_STIMULUS, GOBP_SENSORY_PERCEPTION, ACEVEDO_METHYLATED_IN_LIVER_CANCER_DN, chr19p13, 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, ZHOU_INFLAMMATORY_RESPONSE_FIMA_DN, PDGF_UP.V1_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-2 pathways:

CategoryPathways
Sensory Perception1
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

224 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR10H2ZNF212Q9UDV6508
OR10H2ZNF182P17025506
OR10H2TRMT9BQ9P272474
OR10H2MTMR11A4FU01447
OR10H2VN1R4Q7Z5H5392
OR10H2VN1R2Q8NFZ6364
OR10H2VN1R1Q9GZP7305
OR10H2OMPP47874271
OR10H2TAS2R13Q9NYV9270
OR10H2TAS2R5Q9NYW4246
OR10H2TAS2R31P59538246
OR10H2TAS2R50P59544246
OR10H2TAS2R10Q9NYW0242
OR10H2ADCY3O60266240
OR10H2TAS2R4Q9NYW5223

IntAct

3 interactions, top by confidence:

ABTypeScore
OR10H2ABCD4psi-mi:“MI:0914”(association)0.350
OR10H2LRATD2psi-mi:“MI:0914”(association)0.350

BioGRID (71): ABHD6 (Affinity Capture-MS), SLC43A1 (Affinity Capture-MS), LCLAT1 (Affinity Capture-MS), ATG9A (Affinity Capture-MS), SARAF (Affinity Capture-MS), ATP13A3 (Affinity Capture-MS), PTRH2 (Affinity Capture-MS), TRPM4 (Affinity Capture-MS), NRP2 (Affinity Capture-MS), FADS3 (Affinity Capture-MS), AGPAT3 (Affinity Capture-MS), SLC29A1 (Affinity Capture-MS), SLC12A7 (Affinity Capture-MS), RAB6B (Affinity Capture-MS), CLCN3 (Affinity Capture-MS)

ESM2 similar proteins: A4D2G3, O60403, O76001, O76002, O76100, O95006, O95047, P23269, P23272, P23274, P30953, P30955, P34984, P58173, P59922, P70526, Q13607, Q15619, Q15622, Q5TZ20, Q60890, Q6IF42, Q7Z3T1, Q8N628, Q8NGA6, Q8NGQ2, Q8NGT7, Q8NGT9, Q8NGX0, Q8NGY5, Q8NGZ4, Q8NGZ5, Q8NGZ6, Q8NHA6, Q8VGD6, Q8VGI1, Q95156, Q96R30, Q96R45, Q96R47

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

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance68
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

268 predictions. Top by Δscore:

VariantEffectΔscore
19:15728782:ATTGT:Aacceptor_gain0.7000
19:15728786:T:TAacceptor_gain0.6800
19:15728700:T:Gacceptor_gain0.6700
19:15728707:ATCGT:Aacceptor_gain0.6300
19:15728852:A:Tdonor_gain0.6300
19:15728851:G:GTdonor_gain0.6200
19:15728825:TCAAG:Tacceptor_gain0.6100
19:15728826:CAAGC:Cacceptor_gain0.6100
19:15728711:T:TAacceptor_gain0.6000
19:15728787:G:GAdonor_gain0.5900
19:15728830:CCCAA:Cacceptor_gain0.5900
19:15728409:C:Gdonor_gain0.5800
19:15728700:T:TAacceptor_gain0.5800
19:15728707:ATC:Aacceptor_gain0.5800
19:15728709:C:Aacceptor_gain0.5700
19:15728699:AT:Aacceptor_gain0.5600
19:15728707:A:AGacceptor_gain0.5600
19:15728715:C:CAacceptor_gain0.5600
19:15728720:T:Gacceptor_gain0.5500
19:15728916:CAG:Cacceptor_gain0.5500
19:15728858:A:AGdonor_gain0.5100
19:15728900:TCAGC:Tacceptor_gain0.5100
19:15728901:CAGCC:Cacceptor_gain0.5100
19:15728712:G:Aacceptor_gain0.5000
19:15728899:CTCAG:Cacceptor_gain0.5000
19:15728926:A:Tdonor_gain0.5000
19:15728708:T:Gacceptor_gain0.4900
19:15728918:G:Tacceptor_gain0.4900
19:15728925:G:GTdonor_gain0.4900
19:15728699:A:AGacceptor_gain0.4800

AlphaMissense

2053 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:15728914:T:CF291L0.953
19:15728916:C:AF291L0.953
19:15728916:C:GF291L0.953
19:15728092:T:CF17L0.936
19:15728094:C:AF17L0.936
19:15728094:C:GF17L0.936
19:15728077:T:CF12L0.931
19:15728079:C:AF12L0.931
19:15728079:C:GF12L0.931
19:15728545:T:CF168L0.923
19:15728547:C:AF168L0.923
19:15728547:C:GF168L0.923
19:15728917:A:CS292R0.917
19:15728919:C:AS292R0.917
19:15728919:C:GS292R0.917
19:15728359:A:CS106R0.904
19:15728361:C:AS106R0.904
19:15728361:C:GS106R0.904
19:15728902:A:CS287R0.904
19:15728904:C:AS287R0.904
19:15728904:C:GS287R0.904
19:15728533:T:CF164L0.903
19:15728535:C:AF164L0.903
19:15728535:C:GF164L0.903
19:15728488:T:AW149R0.897
19:15728488:T:CW149R0.897
19:15728572:T:CF177L0.894
19:15728574:T:AF177L0.894
19:15728574:T:GF177L0.894
19:15728509:G:AG156R0.890

dbSNP variants (sampled 300 via entrez): RS1002258663 (19:15727717 A>G), RS1002311012 (19:15727946 C>A,T), RS1003930335 (19:15727026 G>A), RS1004157536 (19:15726488 G>A), RS1004282360 (19:15726746 G>A), RS1005555627 (19:15727980 G>C), RS1005897494 (19:15727702 A>G), RS1006260949 (19:15727479 G>C), RS1008103617 (19:15727073 G>C,T), RS1010014991 (19:15728446 C>T), RS1011229782 (19:15729149 C>T), RS1012401177 (19:15727744 G>A,T), RS1013363071 (19:15726138 C>T), RS1014279164 (19:15726411 C>T), RS1014331345 (19:15726703 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

5 total (human), top 5 by PubMed support.

ChemicalActions (top 5)PubMed papers
Resveratrolaffects cotreatment, decreases expression1
Benzo(a)pyreneaffects methylation1
Plant Extractsaffects cotreatment, decreases expression1
Asbestos, Crocidoliteaffects expression1
Antirheumatic Agentsdecreases 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.