OR7D4
gene geneOn this page
Also known as hg105OR19-B
Summary
OR7D4 (olfactory receptor family 7 subfamily D member 4, HGNC:8380) is a protein-coding gene on chromosome 19p13.2, encoding Olfactory receptor 7D4 (Q8NG98). 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 125958 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 54 total
- MANE Select transcript:
NM_001005191
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:8380 |
| Approved symbol | OR7D4 |
| Name | olfactory receptor family 7 subfamily D member 4 |
| Location | 19p13.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | hg105, OR19-B |
| Ensembl gene | ENSG00000174667 |
| Ensembl biotype | protein_coding |
| OMIM | 611538 |
| Entrez | 125958 |
Gene structure
Transcript identifiers
Ensembl transcripts: 3 — 3 protein_coding
ENST00000308682, ENST00000641244, ENST00000641669
RefSeq mRNA: 1 — MANE Select: NM_001005191
NM_001005191
CCDS: CCDS32901
Canonical transcript exons
ENST00000641669 — 2 exons
| Exon | Start | End |
|---|---|---|
| ENSE00003813804 | 9210276 | 9214850 |
| ENSE00003814226 | 9219200 | 9219589 |
Expression profiles
Bgee: expression breadth tissue_specific, 2 present calls, max score 51.02.
Top tissues by expression
128 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| sural nerve | UBERON:0015488 | 51.02 | gold quality |
| stromal cell of endometrium | CL:0002255 | 47.78 | gold quality |
| ventricular zone | UBERON:0003053 | 43.20 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 41.96 | gold quality |
| colonic epithelium | UBERON:0000397 | 41.22 | gold quality |
| ganglionic eminence | UBERON:0004023 | 40.78 | silver quality |
| cortical plate | UBERON:0005343 | 39.80 | gold quality |
| bone marrow | UBERON:0002371 | 38.89 | gold quality |
| monocyte | CL:0000576 | 38.49 | gold quality |
| leukocyte | CL:0000738 | 38.09 | gold quality |
| calcaneal tendon | UBERON:0003701 | 37.55 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 37.34 | gold quality |
| granulocyte | CL:0000094 | 37.26 | gold quality |
| muscle tissue | UBERON:0002385 | 37.24 | gold quality |
| blood | UBERON:0000178 | 36.57 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| cortex of kidney | UBERON:0001225 | 35.07 | silver quality |
| liver | UBERON:0002107 | 34.85 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 34.79 | gold quality |
| urinary bladder | UBERON:0001255 | 34.41 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 33.78 | gold quality |
| adrenal tissue | UBERON:0018303 | 33.37 | gold quality |
| endometrium | UBERON:0001295 | 33.27 | gold quality |
| lymph node | UBERON:0000029 | 33.17 | gold quality |
| mucosa of stomach | UBERON:0001199 | 32.59 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 32.50 | gold quality |
| placenta | UBERON:0001987 | 32.27 | gold quality |
| myometrium | UBERON:0001296 | 32.08 | gold quality |
| prefrontal cortex | UBERON:0000451 | 31.77 | gold quality |
| muscle of leg | UBERON:0001383 | 31.73 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 5.41 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 6)
- Genotypic variation in OR7D4 accounts for a significant proportion of the valence (pleasantness or unpleasantness) and intensity variance in perception of these steroidal odours (PMID:17873857)
- The results suggested that odor perception between heterosexual partners may have an impact on the development of depression and anxiety, and that it might be influenced by genetic variation in OR7D4. (PMID:21093532)
- This study suggested that OR7D4 sequence variant (rs2878329 G>A) showed evidence of association with reduced levels of adiposity (p=0.03), cognitive dietary restraint (p=0.05) and susceptibility to hunger (p=0.008). (PMID:22044667)
- Data is consistent with the idea that OR7D4 genotype predicts the sensory perception of meat containing androstenone and that genetic variation in an odorant receptor can alter food preferences. (PMID:22567099)
- results suggest non-neutral evolution for an olfactory receptor gene (PMID:26072518)
- Impact of genotypic variations of the androstadienone (AND)-receptor OR7D4, as well as the influence of participant sex and concomitant hormonal fluctuations on AND-action during emotional interference processing, olfactory performance and mood assessments. (PMID:29246659)
Cross-species orthologs
7 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Or7d11 | ENSMUSG00000044454 |
| mus_musculus | Or7d10 | ENSMUSG00000051118 |
| mus_musculus | Or7d9 | ENSMUSG00000059623 |
| rattus_norvegicus | Or7d10 | ENSRNOG00000030569 |
| rattus_norvegicus | ENSRNOG00000073248 | |
| rattus_norvegicus | Or7d11c | ENSRNOG00000077229 |
| rattus_norvegicus | Or7d9 | ENSRNOG00000088878 |
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), OR4S2 (ENSG00000174982), OR4B1 (ENSG00000175619), OR4D11 (ENSG00000176200), OR4K17 (ENSG00000176230)
Protein
Protein identifiers
Olfactory receptor 7D4 — Q8NG98 (reviewed: Q8NG98)
Alternative names: OR19-B, Odorant receptor family subfamily D member 4RT, Olfactory receptor OR19-7
All UniProt accessions (2): Q8NG98, A0A126GVR1
UniProt curated annotations — full annotation on UniProt →
Function. Odorant receptor. Selectively activated by androstenone and the related odorous steroid androstadienone.
Subcellular location. Cell membrane.
Tissue specificity. Nasal olfactory epithelium.
Similarity. Belongs to the G-protein coupled receptor 1 family.
RefSeq proteins (1): NP_001005191* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR000276 | GPCR_Rhodpsn | Family |
| IPR000725 | Olfact_rcpt | Family |
| IPR017452 | GPCR_Rhodpsn_7TM | Domain |
Pfam: PF13853
UniProt features (32 total): sequence variant 14, topological domain 8, transmembrane region 7, chain 1, glycosylation site 1, disulfide bond 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q8NG98-F1 | 88.11 | 0.59 |
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
| ID | Pathway |
|---|---|
| R-HSA-381753 | Olfactory Signaling Pathway |
| R-HSA-9752946 | Expression 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, 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, PEDRIOLI_MIR31_TARGETS_UP, REACTOME_OLFACTORY_SIGNALING_PATHWAY, REACTOME_SENSORY_PERCEPTION, GOBP_DETECTION_OF_CHEMICAL_STIMULUS
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), protein binding (GO:0005515)
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 |
| binding | 1 |
| membrane | 1 |
| cell periphery | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
440 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| OR7D4 | TAS2R60 | P59551 | 447 |
| OR7D4 | VN1R1 | Q9GZP7 | 441 |
| OR7D4 | TAAR5 | O14804 | 436 |
| OR7D4 | SSTR2 | P30874 | 413 |
| OR7D4 | FPR3 | P25089 | 406 |
| OR7D4 | SLC12A6 | Q9UHW9 | 405 |
| OR7D4 | RTP1 | P59025 | 401 |
| OR7D4 | TAS2R38 | P59533 | 400 |
| OR7D4 | TAS2R10 | Q9NYW0 | 399 |
| OR7D4 | CCER1 | Q8TC90 | 391 |
| OR7D4 | SYNE1 | Q8NF91 | 389 |
| OR7D4 | RTP2 | Q5QGT7 | 377 |
| OR7D4 | F2Z2I4 | F2Z2I4 | 369 |
| OR7D4 | DEFB130A | P0DP74 | 368 |
| OR7D4 | CHRM4 | P08173 | 353 |
IntAct
15 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| OR7D4 | UBQLN2 | psi-mi:“MI:0915”(physical association) | 0.560 |
| TUSC5 | OR7D4 | psi-mi:“MI:0915”(physical association) | 0.560 |
| SLC10A6 | OR7D4 | psi-mi:“MI:0915”(physical association) | 0.560 |
| OR7D4 | ECE1 | psi-mi:“MI:0915”(physical association) | 0.370 |
| ECE1 | OR7D4 | psi-mi:“MI:0915”(physical association) | 0.370 |
| OR7D4 | UBQLN2 | psi-mi:“MI:0915”(physical association) | 0.000 |
| TUSC5 | OR7D4 | psi-mi:“MI:0915”(physical association) | 0.000 |
| OR7D4 | SLC10A6 | psi-mi:“MI:0915”(physical association) | 0.000 |
BioGRID (3): OR7D4 (Two-hybrid), TUSC5 (Two-hybrid), UBQLN2 (Two-hybrid)
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: A0A2R8YED5, O14581, O43749, O76099, O95221, P0C626, P0C7N1, P0C7N5, P0DN81, P23266, P23275, P30955, P47890, P58173, P58181, P59922, Q15617, Q15619, Q15622, Q60878, Q60881, Q60895, Q6IEU7, Q6UXT6, Q7TQQ0, Q7Z3T1, Q8N0Y5, Q8N146, Q8N162, Q8N628, Q8NG98, Q8NGA1, Q8NGC2, Q8NGE5, Q8NGF4, Q8NGF8, Q8NGG0, Q8NGG3, Q8NGG4, Q8NGG8
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 | 52 |
| Likely benign | 1 |
| Benign | 1 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
389 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 19:9214158:C:A | donor_gain | 0.6800 |
| 19:9214135:A:AC | donor_gain | 0.6700 |
| 19:9214136:C:CC | donor_gain | 0.6700 |
| 19:9214157:T:A | donor_gain | 0.6600 |
| 19:9214691:G:T | donor_gain | 0.6500 |
| 19:9214238:A:C | acceptor_gain | 0.6300 |
| 19:9214590:A:AC | donor_gain | 0.6300 |
| 19:9214591:C:CC | donor_gain | 0.6300 |
| 19:9214432:TGATG:T | donor_gain | 0.6100 |
| 19:9214082:A:C | acceptor_gain | 0.6000 |
| 19:9213951:T:TA | donor_gain | 0.5900 |
| 19:9214436:G:T | donor_gain | 0.5800 |
| 19:9214688:G:C | donor_gain | 0.5800 |
| 19:9214007:CA:C | donor_gain | 0.5600 |
| 19:9214434:A:AC | donor_gain | 0.5600 |
| 19:9214007:CATCA:C | donor_gain | 0.5500 |
| 19:9214160:C:T | acceptor_gain | 0.5500 |
| 19:9214006:A:AC | donor_gain | 0.5400 |
| 19:9214007:C:CC | donor_gain | 0.5400 |
| 19:9214215:A:T | donor_gain | 0.5400 |
| 19:9214235:CACA:C | acceptor_gain | 0.5400 |
| 19:9214282:TGAGG:T | donor_gain | 0.5400 |
| 19:9214139:GC:G | donor_gain | 0.5300 |
| 19:9214140:CC:C | donor_gain | 0.5300 |
| 19:9214240:A:AC | donor_gain | 0.5300 |
| 19:9214241:C:CC | donor_gain | 0.5300 |
| 19:9214241:CAAGA:C | donor_gain | 0.5300 |
| 19:9214833:T:TA | donor_gain | 0.5300 |
| 19:9214591:CTAG:C | donor_gain | 0.5200 |
| 19:9213933:T:A | donor_gain | 0.5100 |
AlphaMissense
2036 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 19:9214802:A:C | F12L | 0.842 |
| 19:9214802:A:T | F12L | 0.842 |
| 19:9214804:A:G | F12L | 0.842 |
| 19:9214085:G:C | F251L | 0.807 |
| 19:9214085:G:T | F251L | 0.807 |
| 19:9214087:A:G | F251L | 0.807 |
| 19:9214334:G:C | F168L | 0.807 |
| 19:9214334:G:T | F168L | 0.807 |
| 19:9214336:A:G | F168L | 0.807 |
| 19:9213965:G:C | S291R | 0.801 |
| 19:9213965:G:T | S291R | 0.801 |
| 19:9213967:T:G | S291R | 0.801 |
| 19:9214484:C:A | M118I | 0.763 |
| 19:9214484:C:G | M118I | 0.763 |
| 19:9214484:C:T | M118I | 0.763 |
| 19:9213974:G:C | F288L | 0.753 |
| 19:9213974:G:T | F288L | 0.753 |
| 19:9213976:A:G | F288L | 0.753 |
| 19:9214473:C:G | R122P | 0.746 |
| 19:9214624:A:G | C72R | 0.728 |
| 19:9214745:G:C | F31L | 0.719 |
| 19:9214745:G:T | F31L | 0.719 |
| 19:9214747:A:G | F31L | 0.719 |
| 19:9214469:A:C | F123L | 0.716 |
| 19:9214469:A:T | F123L | 0.716 |
| 19:9214471:A:G | F123L | 0.716 |
| 19:9214307:G:C | F177L | 0.714 |
| 19:9214307:G:T | F177L | 0.714 |
| 19:9214309:A:G | F177L | 0.714 |
| 19:9214712:G:C | N42K | 0.710 |
dbSNP variants (sampled 300 via entrez): RS1000162779 (19:9215690 T>C), RS1000518761 (19:9220454 A>G), RS1000622302 (19:9221070 C>A,G,T), RS1000692714 (19:9221456 T>A), RS1001047207 (19:9215164 G>A,T), RS1001076415 (19:9215012 T>C), RS1001218196 (19:9210993 G>T), RS1001388855 (19:9216418 A>T), RS1001568538 (19:9215029 A>G), RS1001689070 (19:9210575 C>T), RS1002761752 (19:9218272 C>T), RS1002954622 (19:9212203 G>A), RS1003293313 (19:9212407 A>G), RS1003427138 (19:9218587 T>C), RS1003665954 (19:9213319 G>A)
Disease associations
OMIM: gene MIM:611538 | 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
2 total (human), top 2 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Endosulfan | decreases expression | 1 |
| Sodium Selenite | decreases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.