OR8J2
gene geneOn this page
Summary
OR8J2 (olfactory receptor family 8 subfamily J member 2 (gene/pseudogene), HGNC:15311) is a protein-coding gene on chromosome 11q12.1, encoding Olfactory receptor 8J2 (Q8NGG1). 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. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional.
Source: NCBI Gene 81169 — RefSeq curated summary.
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:15311 |
| Approved symbol | OR8J2 |
| Name | olfactory receptor family 8 subfamily J member 2 (gene/pseudogene) |
| Location | 11q12.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000254658 |
| Ensembl biotype | protein_coding |
| Entrez | 81169 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding_LoF
ENST00000641465
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000641465 — 2 exons
| Exon | Start | End |
|---|---|---|
| ENSE00003813991 | 56208985 | 56211845 |
| ENSE00003814232 | 56215201 | 56215222 |
Expression profiles
Bgee: expression breadth not_expressed, 0 present calls, max score 37.20.
Top tissues by expression
130 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | 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 | 33.38 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| bone marrow | UBERON:0002371 | 31.74 | gold quality |
| monocyte | CL:0000576 | 31.23 | gold quality |
| muscle tissue | UBERON:0002385 | 31.06 | gold quality |
| sural nerve | UBERON:0015488 | 30.93 | gold quality |
| leukocyte | CL:0000738 | 30.90 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| prefrontal cortex | UBERON:0000451 | 29.04 | gold quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| liver | UBERON:0002107 | 28.04 | gold quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| tonsil | UBERON:0002372 | 27.05 | gold quality |
| islet of Langerhans | UBERON:0000006 | 26.55 | gold quality |
| vermiform appendix | UBERON:0001154 | 26.42 | gold quality |
| blood | UBERON:0000178 | 26.23 | gold quality |
| gall bladder | UBERON:0002110 | 25.98 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 25.89 | gold quality |
| placenta | UBERON:0001987 | 25.81 | gold quality |
| urinary bladder | UBERON:0001255 | 25.72 | gold quality |
| muscle of leg | UBERON:0001383 | 24.85 | gold quality |
| primary visual cortex | UBERON:0002436 | 24.61 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 24.08 | gold quality |
| pancreas | UBERON:0001264 | 23.89 | gold quality |
| kidney | UBERON:0002113 | 23.89 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
Cross-species orthologs
0 orthologs
Paralogs (96): OR5C1 (ENSG00000148215), OR5F1 (ENSG00000149133), OR8K1 (ENSG00000150261), OR5M9 (ENSG00000150269), OR14K1 (ENSG00000153230), OR8J3 (ENSG00000167822), OR5I1 (ENSG00000167825), OR5AU1 (ENSG00000169327), OR9K2 (ENSG00000170605), OR8B12 (ENSG00000170953), OR10H3 (ENSG00000171936), OR8I2 (ENSG00000172154), OR8U1 (ENSG00000172199), OR10V1 (ENSG00000172289), OR5A1 (ENSG00000172320), OR5A2 (ENSG00000172324), OR5B12 (ENSG00000172362), OR5B2 (ENSG00000172365), OR9I1 (ENSG00000172377), OR9G4 (ENSG00000172457), OR5AR1 (ENSG00000172459), OR5AP2 (ENSG00000172464), OR8J1 (ENSG00000172487), OR5B3 (ENSG00000172769), OR10W1 (ENSG00000172772), OR5M3 (ENSG00000174937), OR5J2 (ENSG00000174957), OR10H4 (ENSG00000176231), OR5AN1 (ENSG00000176495), OR14C36 (ENSG00000177174), OR6B3 (ENSG00000178586), OR10Q1 (ENSG00000180475), OR8G2P (ENSG00000181214), OR5AK2 (ENSG00000181273), OR5AK3P (ENSG00000181282), OR5M8 (ENSG00000181371), OR8D4 (ENSG00000181518), OR8H1 (ENSG00000181693), OR8K5 (ENSG00000181752), OR8H3 (ENSG00000181761)
Protein
Protein identifiers
Olfactory receptor 8J2 — Q8NGG1 (reviewed: Q8NGG1)
All UniProt accessions (0):
UniProt curated annotations — full annotation on UniProt →
Function. Odorant receptor.
Subcellular location. Membrane.
Polymorphism. A stop codon in the gene coding for this protein at position Arg-64 is responsible for functional diversity thus producing a pseudogene.
Similarity. Belongs to the G-protein coupled receptor 1 family.
RefSeq proteins (0): (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR000276 | GPCR_Rhodpsn | Family |
| IPR000725 | Olfact_rcpt | Family |
| IPR017452 | GPCR_Rhodpsn_7TM | Domain |
Pfam: PF13853
UniProt features (19 total): topological domain 8, transmembrane region 7, glycosylation site 2, chain 1, disulfide bond 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q8NGG1-F1 | 89.21 | 0.65 |
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
Glycosylation sites (2): 5, 265
Function
Pathways and Gene Ontology
Reactome pathways
1 pathways
| ID | Pathway |
|---|---|
| R-HSA-9752946 | Expression and translocation of olfactory receptors |
MSigDB gene sets: 16 (showing top):
GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, GOBP_DETECTION_OF_STIMULUS, GOBP_SENSORY_PERCEPTION, 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, HMGA1_TARGET_GENES, REACTOME_OLFACTORY_SIGNALING_PATHWAY, REACTOME_SENSORY_PERCEPTION, GOBP_DETECTION_OF_CHEMICAL_STIMULUS, GOMF_MOLECULAR_TRANSDUCER_ACTIVITY, chr11q12
GO Biological Process (0):
GO Molecular Function (2): G protein-coupled receptor activity (GO:0004930), olfactory receptor activity (GO:0004984)
GO Cellular Component (1): membrane (GO:0016020)
Reactome top-level categories
Rollup of top-1 pathways:
| Category | Pathways |
|---|---|
| Olfactory Signaling Pathway | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| transmembrane signaling receptor activity | 2 |
| G protein-coupled receptor signaling pathway | 1 |
| detection of chemical stimulus involved in sensory perception of smell | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
0 interactions, top by confidence:
ESM2 similar proteins: A0A2R8YED5, A6ND48, B2RN74, O60412, O76099, O76100, O95047, P23271, P23272, P34982, P37069, P37072, P47884, P47890, P58170, Q15622, Q60879, Q8NG84, Q8NG94, Q8NG95, Q8NG98, Q8NG99, Q8NGA0, Q8NGA2, Q8NGE0, Q8NGG1, Q8NGL0, Q8NGP2, Q8NGS2, Q8NGW1, Q8NGZ2, Q8NGZ5, Q8NH06, Q8NH07, Q8NH80, Q8NHA4, Q8NHC7, Q8VEY3, Q8VFC9, Q8WZA6
Diamond homologs: A6NCV1, A6NDL8, A6NF89, A6NIJ9, A6NJZ3, A6NL08, A6NL26, A6NM76, O76001, O76002, O76100, O95007, P0C623, P0C626, P23266, P23267, P23272, P23274, P30953, P30955, P34985, P58173, P59922, P70526, Q13606, Q5TZ20, Q60882, Q60890, Q6UXT6, Q7TQQ0, Q7Z3T1, Q8N146, Q8N148, Q8N162, Q8N628, Q8NGA1, Q8NGC5, Q8NGE1, Q8NGE2, Q8NGE5
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
172 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 11:56210981:CAGGG:C | acceptor_gain | 0.8000 |
| 11:56211645:A:C | donor_gain | 0.7600 |
| 11:56211640:A:AC | donor_gain | 0.6700 |
| 11:56211176:C:CT | acceptor_gain | 0.6100 |
| 11:56211209:CCCTG:C | acceptor_loss | 0.5800 |
| 11:56211210:CCTG:C | acceptor_loss | 0.5800 |
| 11:56211211:C:CC | acceptor_gain | 0.5800 |
| 11:56211211:CTGA:C | acceptor_loss | 0.5800 |
| 11:56211212:T:C | acceptor_loss | 0.5700 |
| 11:56211698:C:A | donor_gain | 0.5600 |
| 11:56211788:CTCCG:C | donor_gain | 0.5600 |
| 11:56211789:TCCGT:T | donor_gain | 0.5600 |
| 11:56211790:CCGTC:C | donor_gain | 0.5600 |
| 11:56211142:T:TG | acceptor_gain | 0.5500 |
| 11:56211209:CC:C | acceptor_gain | 0.5500 |
| 11:56211210:CC:C | acceptor_gain | 0.5500 |
| 11:56211671:A:AC | donor_gain | 0.5500 |
| 11:56211672:C:CC | donor_gain | 0.5500 |
| 11:56211774:C:CA | donor_gain | 0.5500 |
| 11:56211143:C:A | acceptor_gain | 0.5300 |
| 11:56211219:A:C | acceptor_loss | 0.5300 |
| 11:56210982:A:T | acceptor_gain | 0.5100 |
| 11:56211048:A:C | acceptor_gain | 0.5100 |
| 11:56211038:T:TC | acceptor_gain | 0.4800 |
| 11:56211418:C:CT | donor_gain | 0.4800 |
| 11:56211419:T:TT | donor_gain | 0.4800 |
| 11:56211220:TAAAG:T | acceptor_loss | 0.4700 |
| 11:56211221:AAAGA:A | acceptor_loss | 0.4700 |
| 11:56211333:A:T | donor_gain | 0.4700 |
| 11:56210985:G:GC | acceptor_gain | 0.4600 |
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1000778578 (11:56212532 C>A), RS1000884269 (11:56214684 T>C), RS1001137826 (11:56209826 A>G), RS1001464727 (11:56209564 T>C), RS1001612942 (11:56212273 C>A), RS1001792340 (11:56212049 G>T), RS1002485747 (11:56212121 G>A,C), RS1002516130 (11:56215318 C>T), RS1002765992 (11:56212909 C>A,T), RS1003156270 (11:56209659 A>T), RS1003685454 (11:56211244 A>G), RS1003724399 (11:56216589 A>C), RS1004586982 (11:56210585 C>A,T), RS1004637894 (11:56210315 C>A), RS1005002126 (11:56216712 A>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.