OR7G2

gene
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Also known as OST260

Summary

OR7G2 (olfactory receptor family 7 subfamily G member 2, HGNC:8466) is a protein-coding gene on chromosome 19p13.2, encoding Olfactory receptor 7G2 (Q8NG99). Odorant receptor. It is a selective cancer dependency (DepMap: 16.0% of cell lines).

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 390882 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 54 total
  • Cancer dependency (DepMap): dependent in 16.0% of screened cell lines
  • MANE Select transcript: NM_001005193

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:8466
Approved symbolOR7G2
Nameolfactory receptor family 7 subfamily G member 2
Location19p13.2
Locus typegene with protein product
StatusApproved
AliasesOST260
Ensembl geneENSG00000170923
Ensembl biotypeprotein_coding
Entrez390882

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000641081

RefSeq mRNA: 1 — MANE Select: NM_001005193 NM_001005193

CCDS: CCDS32897

Canonical transcript exons

ENST00000641081 — 2 exons

ExonStartEnd
ENSE0000381180891073149107475
ENSE0000381196691004079103259

Expression profiles

Bgee: expression breadth tissue_specific, 2 present calls, max score 41.68.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
hindlimb stylopod muscleUBERON:000425241.68gold quality
colonic epitheliumUBERON:000039741.02gold quality
sural nerveUBERON:001548840.86gold quality
popliteal arteryUBERON:000225040.75silver quality
tibial arteryUBERON:000761040.71silver quality
granulocyteCL:000009440.39gold quality
ventricular zoneUBERON:000305340.15gold quality
stromal cell of endometriumCL:000225539.58gold quality
smooth muscle tissueUBERON:000113538.39gold quality
leukocyteCL:000073838.33gold quality
monocyteCL:000057638.11gold quality
lower esophagus mucosaUBERON:003583438.10gold quality
bone marrowUBERON:000237137.88gold quality
muscle tissueUBERON:000238536.65gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
bloodUBERON:000017836.08gold quality
ganglionic eminenceUBERON:000402335.49gold quality
liverUBERON:000210735.29gold quality
skeletal muscle tissueUBERON:000113434.80gold quality
mucosa of transverse colonUBERON:000499134.51gold quality
ascending aortaUBERON:000149633.84gold quality
thoracic aortaUBERON:000151533.73gold quality
primary visual cortexUBERON:000243633.19gold quality
body of pancreasUBERON:000115032.93gold quality
lower esophagusUBERON:001347332.75gold quality
lower esophagus muscularis layerUBERON:003583332.68gold quality
ovaryUBERON:000099232.56gold quality
right lobe of liverUBERON:000111432.49gold quality
subcutaneous adipose tissueUBERON:000219032.47gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.09

Regulation

Is transcription factor: no

Functional genomics

DepMap (CRISPR cell-line fitness): dependent in 16.0% of screened cell lines.

Cross-species orthologs

9 orthologs

OrganismSymbolGene ID
mus_musculusOr7g20ENSMUSG00000045204
mus_musculusOr7g28ENSMUSG00000058692
mus_musculusOr7g29ENSMUSG00000059821
mus_musculusOr7g27ENSMUSG00000061614
mus_musculusOr7g16ENSMUSG00000078116
rattus_norvegicusOr7g16ENSRNOG00000006439
rattus_norvegicusOr7g29ENSRNOG00000006577
rattus_norvegicusOr7g41ENSRNOG00000030845
rattus_norvegicusOr7g20ENSRNOG00000076463

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), 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), OR4K17 (ENSG00000176230)

Protein

Protein identifiers

Olfactory receptor 7G2Q8NG99 (reviewed: Q8NG99)

Alternative names: OST260, Olfactory receptor 19-13, Olfactory receptor OR19-6

All UniProt accessions (2): A0A126GW43, Q8NG99

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_001005193* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain

Pfam: PF13853

UniProt features (21 total): topological domain 8, transmembrane region 7, glycosylation site 2, chain 1, disulfide bond 1, sequence variant 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8NG99-F185.650.50

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, 89

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: 21 (showing top): GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, KEGG_OLFACTORY_TRANSDUCTION, GOBP_DETECTION_OF_STIMULUS, GOBP_SENSORY_PERCEPTION, chr19p13, GOMF_OLFACTORY_RECEPTOR_ACTIVITY, RAY_TUMORIGENESIS_BY_ERBB2_CDC25A_UP, GOMF_TRANSMEMBRANE_SIGNALING_RECEPTOR_ACTIVITY, GOMF_G_PROTEIN_COUPLED_RECEPTOR_ACTIVITY, MARTENS_TRETINOIN_RESPONSE_DN, GOBP_SENSORY_PERCEPTION_OF_SMELL, GOBP_G_PROTEIN_COUPLED_RECEPTOR_SIGNALING_PATHWAY, GOBP_DETECTION_OF_STIMULUS_INVOLVED_IN_SENSORY_PERCEPTION, RAO_BOUND_BY_SALL4_ISOFORM_A, RAO_BOUND_BY_SALL4_ISOFORM_B

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-2 pathways:

CategoryPathways
Sensory Perception1
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

130 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR7G2KANSL1LA0AUZ9513
OR7G2LRRC45Q96CN5459
OR7G2MMP27Q9H306429
OR7G2MRPS18BQ9Y676415
OR7G2CFAP276Q5T5A4415
OR7G2ANO7Q6IWH7399
OR7G2L1TD1Q5T7N2396
OR7G2PARP8Q8N3A8374
OR7G2RPTNQ6XPR3371
OR7G2BHLHE22Q8NFJ8363
OR7G2ARHGEF40Q8TER5344
OR7G2MLF1P58340321
OR7G2NACC1Q96RE7306
OR7G2FOXE3Q13461302
OR7G2CATSPERTQ53TS8288

IntAct

6 interactions, top by confidence:

ABTypeScore
OR7G2ECE1psi-mi:“MI:0915”(physical association)0.370
ECE1OR7G2psi-mi:“MI:0915”(physical association)0.370

ESM2 similar proteins: A0A2R8YED5, A6NM03, O14581, O60412, O76099, O95006, O95047, O95371, P34982, P34984, P47884, P58170, Q15619, Q15622, Q5TZ20, Q60883, Q60887, Q60891, Q6IFH4, Q7Z3T1, Q8N628, Q8NG84, Q8NG95, Q8NG98, Q8NG99, Q8NGA0, Q8NGA1, Q8NGA2, Q8NGQ5, Q8NGR9, Q8NGS1, Q8NGS2, Q8NGS3, Q8NGV0, Q8NGW1, Q8NGX1, Q8NH06, Q8NH80, Q8NHA4, Q95157

Diamond homologs: A0A3B3IT45, A6NGY5, A6NMU1, A6NND4, O43749, O60431, O88628, P0C626, P0C646, P0C7T3, P0DN81, P23266, P23272, P23273, P23274, P30953, P30955, P58181, P70526, Q13607, Q6IF63, Q6IFG1, Q6W049, Q8NG95, Q8NG99, Q8NGA0, Q8NGA1, Q8NGC4, Q8NGF0, Q8NGF1, Q8NGF3, Q8NGH5, Q8NGH6, Q8NGH7, Q8NGH8, Q8NGH9, Q8NGI0, Q8NGI1, Q8NGI2, Q8NGI3

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 significance51
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

412 predictions. Top by Δscore:

VariantEffectΔscore
19:9102984:G:Cdonor_gain0.7300
19:9103240:C:Adonor_gain0.7200
19:9102938:G:Cdonor_gain0.7000
19:9103136:CAAG:Cdonor_gain0.6800
19:9103138:A:ACdonor_gain0.6700
19:9102959:TGAG:Tdonor_gain0.6600
19:9102966:G:Cdonor_gain0.6600
19:9102878:G:Cdonor_gain0.6500
19:9102961:A:ACdonor_gain0.6400
19:9102417:A:ACdonor_gain0.6300
19:9102418:C:CCdonor_gain0.6300
19:9102912:T:Adonor_gain0.6200
19:9102964:A:ACdonor_gain0.6200
19:9102965:C:CCdonor_gain0.6200
19:9103144:TGG:Tdonor_gain0.6200
19:9102955:AG:Adonor_gain0.6100
19:9103135:CCAA:Cdonor_gain0.6100
19:9103143:A:Cdonor_gain0.6100
19:9102956:G:GAdonor_gain0.6000
19:9102413:CA:Cdonor_gain0.5700
19:9102483:G:Adonor_gain0.5700
19:9102886:AGG:Adonor_gain0.5700
19:9102362:ATT:Adonor_gain0.5600
19:9102413:CATCA:Cdonor_gain0.5600
19:9103154:CAGG:Cdonor_gain0.5600
19:9102957:CCTGA:Cdonor_gain0.5500
19:9103185:T:TAdonor_gain0.5500
19:9102532:CTG:Cdonor_gain0.5400
19:9102677:A:Cdonor_gain0.5400
19:9102392:C:CTacceptor_gain0.5300

AlphaMissense

2110 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:9103208:G:CF12L0.855
19:9103208:G:TF12L0.855
19:9103210:A:GF12L0.855
19:9102740:G:CF168L0.817
19:9102740:G:TF168L0.817
19:9102742:A:GF168L0.817
19:9103022:G:CS74R0.802
19:9103022:G:TS74R0.802
19:9103024:T:GS74R0.802
19:9102491:G:CF251L0.793
19:9102491:G:TF251L0.793
19:9102493:A:GF251L0.793
19:9102710:G:CF178L0.773
19:9102710:G:TF178L0.773
19:9102712:A:GF178L0.773
19:9102879:C:GR122P0.757
19:9102788:A:CS152R0.754
19:9102788:A:TS152R0.754
19:9102790:T:GS152R0.754
19:9102713:G:CF177L0.748
19:9102713:G:TF177L0.748
19:9102715:A:GF177L0.748
19:9102890:C:AM118I0.743
19:9102890:C:GM118I0.743
19:9102890:C:TM118I0.743
19:9102380:A:CF288L0.727
19:9102380:A:TF288L0.727
19:9102382:A:GF288L0.727
19:9102371:A:CS291R0.724
19:9102371:A:TS291R0.724

dbSNP variants (sampled 300 via entrez): RS1000041975 (19:9104658 T>C), RS1000093746 (19:9104881 G>A), RS1000941627 (19:9100320 G>A,C), RS1001099250 (19:9106337 A>C,G), RS1001528959 (19:9101787 A>G), RS1001560574 (19:9101496 C>A), RS1002065614 (19:9107441 G>A), RS1002087306 (19:9107868 G>A), RS1002116379 (19:9107628 T>C), RS1002459395 (19:9107662 C>T), RS1003070552 (19:9109331 G>A), RS1003206201 (19:9100338 A>G), RS1003237547 (19:9100654 G>A,T), RS1004569096 (19:9105988 TAC>T), RS1004677393 (19:9099954 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

2 associations (top):

StudyTraitp-value
GCST003542_87Night sleep phenotypes5.000000e-06
GCST011053_12Neuroblastoma (pediatric)2.000000e-13

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

2 total (human), top 2 by PubMed support.

ChemicalActions (top 5)PubMed papers
butylbenzyl phthalateincreases expression1
Benzo(a)pyrenedecreases methylation1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): neuroblastoma