OR7G2
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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
| Field | Value |
|---|---|
| HGNC ID | HGNC:8466 |
| Approved symbol | OR7G2 |
| Name | olfactory receptor family 7 subfamily G member 2 |
| Location | 19p13.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | OST260 |
| Ensembl gene | ENSG00000170923 |
| Ensembl biotype | protein_coding |
| Entrez | 390882 |
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
| Exon | Start | End |
|---|---|---|
| ENSE00003811808 | 9107314 | 9107475 |
| ENSE00003811966 | 9100407 | 9103259 |
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):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| hindlimb stylopod muscle | UBERON:0004252 | 41.68 | gold quality |
| colonic epithelium | UBERON:0000397 | 41.02 | gold quality |
| sural nerve | UBERON:0015488 | 40.86 | gold quality |
| popliteal artery | UBERON:0002250 | 40.75 | silver quality |
| tibial artery | UBERON:0007610 | 40.71 | silver quality |
| granulocyte | CL:0000094 | 40.39 | gold quality |
| ventricular zone | UBERON:0003053 | 40.15 | gold quality |
| stromal cell of endometrium | CL:0002255 | 39.58 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 38.39 | gold quality |
| leukocyte | CL:0000738 | 38.33 | gold quality |
| monocyte | CL:0000576 | 38.11 | gold quality |
| lower esophagus mucosa | UBERON:0035834 | 38.10 | gold quality |
| bone marrow | UBERON:0002371 | 37.88 | gold quality |
| muscle tissue | UBERON:0002385 | 36.65 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| blood | UBERON:0000178 | 36.08 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| liver | UBERON:0002107 | 35.29 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 34.80 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 34.51 | gold quality |
| ascending aorta | UBERON:0001496 | 33.84 | gold quality |
| thoracic aorta | UBERON:0001515 | 33.73 | gold quality |
| primary visual cortex | UBERON:0002436 | 33.19 | gold quality |
| body of pancreas | UBERON:0001150 | 32.93 | gold quality |
| lower esophagus | UBERON:0013473 | 32.75 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 32.68 | gold quality |
| ovary | UBERON:0000992 | 32.56 | gold quality |
| right lobe of liver | UBERON:0001114 | 32.49 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 32.47 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 4.09 |
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
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Or7g20 | ENSMUSG00000045204 |
| mus_musculus | Or7g28 | ENSMUSG00000058692 |
| mus_musculus | Or7g29 | ENSMUSG00000059821 |
| mus_musculus | Or7g27 | ENSMUSG00000061614 |
| mus_musculus | Or7g16 | ENSMUSG00000078116 |
| rattus_norvegicus | Or7g16 | ENSRNOG00000006439 |
| rattus_norvegicus | Or7g29 | ENSRNOG00000006577 |
| rattus_norvegicus | Or7g41 | ENSRNOG00000030845 |
| rattus_norvegicus | Or7g20 | ENSRNOG00000076463 |
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 7G2 — Q8NG99 (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)
| ID | Name | Type |
|---|---|---|
| IPR000276 | GPCR_Rhodpsn | Family |
| IPR000725 | Olfact_rcpt | Family |
| IPR017452 | GPCR_Rhodpsn_7TM | Domain |
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)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q8NG99-F1 | 85.65 | 0.50 |
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
| ID | Pathway |
|---|---|
| R-HSA-381753 | Olfactory Signaling Pathway |
| R-HSA-9752946 | Expression 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:
| Category | Pathways |
|---|---|
| Sensory Perception | 1 |
| Olfactory Signaling Pathway | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| transmembrane signaling receptor activity | 2 |
| cell communication | 1 |
| cellular process | 1 |
| signaling | 1 |
| regulation of cellular process | 1 |
| cellular response to stimulus | 1 |
| G protein-coupled receptor activity | 1 |
| signal transduction | 1 |
| sensory perception of chemical stimulus | 1 |
| sensory perception of smell | 1 |
| detection of chemical stimulus involved in sensory perception | 1 |
| G protein-coupled receptor signaling pathway | 1 |
| detection of chemical stimulus involved in sensory perception of smell | 1 |
| membrane | 1 |
| cell periphery | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
130 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| OR7G2 | KANSL1L | A0AUZ9 | 513 |
| OR7G2 | LRRC45 | Q96CN5 | 459 |
| OR7G2 | MMP27 | Q9H306 | 429 |
| OR7G2 | MRPS18B | Q9Y676 | 415 |
| OR7G2 | CFAP276 | Q5T5A4 | 415 |
| OR7G2 | ANO7 | Q6IWH7 | 399 |
| OR7G2 | L1TD1 | Q5T7N2 | 396 |
| OR7G2 | PARP8 | Q8N3A8 | 374 |
| OR7G2 | RPTN | Q6XPR3 | 371 |
| OR7G2 | BHLHE22 | Q8NFJ8 | 363 |
| OR7G2 | ARHGEF40 | Q8TER5 | 344 |
| OR7G2 | MLF1 | P58340 | 321 |
| OR7G2 | NACC1 | Q96RE7 | 306 |
| OR7G2 | FOXE3 | Q13461 | 302 |
| OR7G2 | CATSPERT | Q53TS8 | 288 |
IntAct
6 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| OR7G2 | ECE1 | psi-mi:“MI:0915”(physical association) | 0.370 |
| ECE1 | OR7G2 | psi-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):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 51 |
| Likely benign | 3 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
412 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 19:9102984:G:C | donor_gain | 0.7300 |
| 19:9103240:C:A | donor_gain | 0.7200 |
| 19:9102938:G:C | donor_gain | 0.7000 |
| 19:9103136:CAAG:C | donor_gain | 0.6800 |
| 19:9103138:A:AC | donor_gain | 0.6700 |
| 19:9102959:TGAG:T | donor_gain | 0.6600 |
| 19:9102966:G:C | donor_gain | 0.6600 |
| 19:9102878:G:C | donor_gain | 0.6500 |
| 19:9102961:A:AC | donor_gain | 0.6400 |
| 19:9102417:A:AC | donor_gain | 0.6300 |
| 19:9102418:C:CC | donor_gain | 0.6300 |
| 19:9102912:T:A | donor_gain | 0.6200 |
| 19:9102964:A:AC | donor_gain | 0.6200 |
| 19:9102965:C:CC | donor_gain | 0.6200 |
| 19:9103144:TGG:T | donor_gain | 0.6200 |
| 19:9102955:AG:A | donor_gain | 0.6100 |
| 19:9103135:CCAA:C | donor_gain | 0.6100 |
| 19:9103143:A:C | donor_gain | 0.6100 |
| 19:9102956:G:GA | donor_gain | 0.6000 |
| 19:9102413:CA:C | donor_gain | 0.5700 |
| 19:9102483:G:A | donor_gain | 0.5700 |
| 19:9102886:AGG:A | donor_gain | 0.5700 |
| 19:9102362:ATT:A | donor_gain | 0.5600 |
| 19:9102413:CATCA:C | donor_gain | 0.5600 |
| 19:9103154:CAGG:C | donor_gain | 0.5600 |
| 19:9102957:CCTGA:C | donor_gain | 0.5500 |
| 19:9103185:T:TA | donor_gain | 0.5500 |
| 19:9102532:CTG:C | donor_gain | 0.5400 |
| 19:9102677:A:C | donor_gain | 0.5400 |
| 19:9102392:C:CT | acceptor_gain | 0.5300 |
AlphaMissense
2110 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 19:9103208:G:C | F12L | 0.855 |
| 19:9103208:G:T | F12L | 0.855 |
| 19:9103210:A:G | F12L | 0.855 |
| 19:9102740:G:C | F168L | 0.817 |
| 19:9102740:G:T | F168L | 0.817 |
| 19:9102742:A:G | F168L | 0.817 |
| 19:9103022:G:C | S74R | 0.802 |
| 19:9103022:G:T | S74R | 0.802 |
| 19:9103024:T:G | S74R | 0.802 |
| 19:9102491:G:C | F251L | 0.793 |
| 19:9102491:G:T | F251L | 0.793 |
| 19:9102493:A:G | F251L | 0.793 |
| 19:9102710:G:C | F178L | 0.773 |
| 19:9102710:G:T | F178L | 0.773 |
| 19:9102712:A:G | F178L | 0.773 |
| 19:9102879:C:G | R122P | 0.757 |
| 19:9102788:A:C | S152R | 0.754 |
| 19:9102788:A:T | S152R | 0.754 |
| 19:9102790:T:G | S152R | 0.754 |
| 19:9102713:G:C | F177L | 0.748 |
| 19:9102713:G:T | F177L | 0.748 |
| 19:9102715:A:G | F177L | 0.748 |
| 19:9102890:C:A | M118I | 0.743 |
| 19:9102890:C:G | M118I | 0.743 |
| 19:9102890:C:T | M118I | 0.743 |
| 19:9102380:A:C | F288L | 0.727 |
| 19:9102380:A:T | F288L | 0.727 |
| 19:9102382:A:G | F288L | 0.727 |
| 19:9102371:A:C | S291R | 0.724 |
| 19:9102371:A:T | S291R | 0.724 |
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):
| Study | Trait | p-value |
|---|---|---|
| GCST003542_87 | Night sleep phenotypes | 5.000000e-06 |
| GCST011053_12 | Neuroblastoma (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.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| butylbenzyl phthalate | increases expression | 1 |
| Benzo(a)pyrene | decreases methylation | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): neuroblastoma