OR4N4C
gene geneOn this page
Summary
OR4N4C (olfactory receptor family 4 subfamily N member 4C, HGNC:55110) is a protein-coding gene on chromosome 15q11.2, encoding Olfactory receptor 4N4C (A0A096LPK9). Odorant receptor.
Predicted to enable olfactory receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway and detection of chemical stimulus involved in sensory perception of smell. Predicted to be located in membrane. Predicted to be active in plasma membrane.
Source: NCBI Gene 105369274 — RefSeq curated summary.
At a glance
- MANE Select transcript:
NM_001365389
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:55110 |
| Approved symbol | OR4N4C |
| Name | olfactory receptor family 4 subfamily N member 4C |
| Location | 15q11.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000279408 |
| Ensembl biotype | protein_coding |
| Entrez | 105369274 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000623441
RefSeq mRNA: 1 — MANE Select: NM_001365389
NM_001365389
CCDS: CCDS91961
Canonical transcript exons
ENST00000623441 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00003760045 | 21651844 | 21652968 |
Expression profiles
Bgee: expression breadth tissue_specific, 7 present calls, max score 88.16.
Top tissues by expression
120 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 88.16 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 85.47 | gold quality |
| left testis | UBERON:0004533 | 48.60 | gold quality |
| testis | UBERON:0000473 | 47.70 | gold quality |
| right testis | UBERON:0004534 | 43.31 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 34.95 | gold quality |
| muscle tissue | UBERON:0002385 | 32.22 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| bone marrow | UBERON:0002371 | 31.74 | gold quality |
| sural nerve | UBERON:0015488 | 30.93 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| prefrontal cortex | UBERON:0000451 | 29.38 | gold quality |
| liver | UBERON:0002107 | 28.32 | gold quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| urinary bladder | UBERON:0001255 | 28.00 | gold quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 27.56 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 27.16 | gold quality |
| tonsil | UBERON:0002372 | 27.05 | gold quality |
| muscle of leg | UBERON:0001383 | 26.60 | gold quality |
| islet of Langerhans | UBERON:0000006 | 26.55 | gold quality |
| vermiform appendix | UBERON:0001154 | 26.42 | gold quality |
| blood | UBERON:0000178 | 26.33 | gold quality |
| leukocyte | CL:0000738 | 26.04 | gold quality |
| gall bladder | UBERON:0002110 | 25.98 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.16 |
Regulation
Is transcription factor: no
Cross-species orthologs
4 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Or4n4b | ENSMUSG00000090874 |
| mus_musculus | Or4n4 | ENSMUSG00000091873 |
| rattus_norvegicus | Or4n4 | ENSRNOG00000047419 |
| rattus_norvegicus | Or4n4 | ENSRNOG00000077425 |
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), OR7D4 (ENSG00000174667), OR4S2 (ENSG00000174982), OR4B1 (ENSG00000175619), OR4D11 (ENSG00000176200)
Protein
Protein identifiers
Olfactory receptor 4N4C — A0A096LPK9 (reviewed: A0A096LPK9)
All UniProt accessions (1): A0A096LPK9
UniProt curated annotations — full annotation on UniProt →
Function. Odorant receptor.
Subcellular location. Membrane.
Similarity. Belongs to the G-protein coupled receptor 1 family.
RefSeq proteins (1): NP_001352318* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR000276 | GPCR_Rhodpsn | Family |
| IPR000725 | Olfact_rcpt | Family |
| IPR017452 | GPCR_Rhodpsn_7TM | Domain |
| IPR050427 | Olfactory_Receptors | Family |
Pfam: PF13853
UniProt features (17 total): topological domain 8, transmembrane region 7, chain 1, disulfide bond 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A0A096LPK9-F1 | 84.93 | 0.33 |
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
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 1 (showing top):
chr15q11
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)
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
40 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| OR4N4C | ZNF317 | Q96PQ6 | 507 |
| OR4N4C | ATMIN | O43313 | 320 |
| OR4N4C | PDE1A | P54750 | 248 |
| OR4N4C | PTPRT | O14522 | 223 |
| OR4N4C | NFATC3 | Q12968 | 167 |
| OR4N4C | TAS2R1 | Q9NYW7 | 159 |
| OR4N4C | HAUS3 | Q68CZ6 | 73 |
| OR4N4C | ARRB2 | P32121 | 56 |
| OR4N4C | ARRB1 | P49407 | 56 |
| OR4N4C | GNAL | P38405 | 54 |
| OR4N4C | GNAS | Q5JWF2 | 54 |
| OR4N4C | PRKACA | P17612 | 42 |
| OR4N4C | GRK2 | P25098 | 42 |
| OR4N4C | GRK3 | P35626 | 42 |
| OR4N4C | PRKACB | P22694 | 42 |
| OR4N4C | PRKACG | P22612 | 42 |
IntAct
0 interactions, top by confidence:
ESM2 similar proteins: A0A096LPK9, A0A0X1KG70, A6NHA9, A6NMZ5, P0C604, P0C623, P0C645, P0DN82, P58180, P58182, Q15615, Q60881, Q6IF82, Q8IXE1, Q8N0Y3, Q8NGA8, Q8NGB4, Q8NGB6, Q8NGC2, Q8NGC3, Q8NGD0, Q8NGD1, Q8NGD2, Q8NGD5, Q8NGE8, Q8NGF4, Q8NGF8, Q8NGF9, Q8NGI4, Q8NGI6, Q8NGJ0, Q8NGJ1, Q8NGL6, Q8NGM1, Q8NGN0, Q8NGN8, Q8NGX5, Q8NH05, Q8NH42, Q8NH49
Diamond homologs: A0A096LPK9, A0A0X1KG70, A6NHA9, A6NMZ5, O60412, O76099, O95013, P0C604, P0C623, P0C645, P0DN82, P23270, P23275, P58173, P58180, P58182, Q15615, Q60878, Q60881, Q60888, Q6IEV9, Q6IEY1, Q6IF82, Q7TQQ0, Q8IXE1, Q8N0Y3, Q8N628, Q8NGA8, Q8NGB2, Q8NGB4, Q8NGB6, Q8NGB8, Q8NGB9, Q8NGC2, Q8NGC3, Q8NGC4, Q8NGC6, Q8NGD0, Q8NGD1, Q8NGD2
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
2084 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 15:21651968:T:C | F12L | 0.866 |
| 15:21651970:T:A | F12L | 0.866 |
| 15:21651970:T:G | F12L | 0.866 |
| 15:21652436:T:C | F168L | 0.847 |
| 15:21652438:T:A | F168L | 0.847 |
| 15:21652438:T:G | F168L | 0.847 |
| 15:21652463:T:C | F177L | 0.784 |
| 15:21652465:C:A | F177L | 0.784 |
| 15:21652465:C:G | F177L | 0.784 |
| 15:21652685:T:C | F251L | 0.752 |
| 15:21652687:T:A | F251L | 0.752 |
| 15:21652687:T:G | F251L | 0.752 |
| 15:21652238:T:C | F102L | 0.741 |
| 15:21652240:T:A | F102L | 0.741 |
| 15:21652240:T:G | F102L | 0.741 |
| 15:21652718:T:C | F262L | 0.716 |
| 15:21652720:C:A | F262L | 0.716 |
| 15:21652720:C:G | F262L | 0.716 |
| 15:21652466:T:C | F178L | 0.707 |
| 15:21652468:C:A | F178L | 0.707 |
| 15:21652468:C:G | F178L | 0.707 |
| 15:21652016:T:C | F28L | 0.706 |
| 15:21652018:T:A | F28L | 0.706 |
| 15:21652018:T:G | F28L | 0.706 |
| 15:21651969:T:C | F12S | 0.684 |
| 15:21652565:T:C | F211L | 0.657 |
| 15:21652567:T:A | F211L | 0.657 |
| 15:21652567:T:G | F211L | 0.657 |
| 15:21652769:T:C | F279L | 0.638 |
| 15:21652771:T:A | F279L | 0.638 |
dbSNP variants (sampled 300 via entrez): RS1157556971 (15:21653357 T>G), RS1157576207 (15:21652317 G>A,T), RS1159079896 (15:21652931 C>A,G,T), RS1159794775 (15:21651932 G>A), RS1160876106 (15:21653400 ATAAG>A), RS1161840858 (15:21650292 T>A,C,G), RS1162623432 (15:21652040 C>T), RS1162752295 (15:21653031 T>C), RS1163834089 (15:21653409 A>ATATT), RS1164667590 (15:21652532 G>A,T), RS1165692911 (15:21653151 T>C), RS1166150950 (15:21650355 C>G), RS1166522769 (15:21652140 T>C), RS1166950827 (15:21652661 C>G,T), RS1168397675 (15:21650473 C>G)
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)
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.