TAS2R9
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Also known as T2R9TRB6
Summary
TAS2R9 (taste 2 receptor member 9, HGNC:14917) is a protein-coding gene on chromosome 12p13.2, encoding Taste receptor type 2 member 9 (Q9NYW1). Gustducin-coupled receptor implicated in the perception of bitter compounds in the oral cavity and the gastrointestinal tract.
This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13.
Source: NCBI Gene 50835 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 49 total
- Druggable target: yes — 1 molecules with ChEMBL bioactivity
- MANE Select transcript:
NM_023917
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:14917 |
| Approved symbol | TAS2R9 |
| Name | taste 2 receptor member 9 |
| Location | 12p13.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | T2R9, TRB6 |
| Ensembl gene | ENSG00000121381 |
| Ensembl biotype | protein_coding |
| OMIM | 604795 |
| Entrez | 50835 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000240691
RefSeq mRNA: 1 — MANE Select: NM_023917
NM_023917
CCDS: CCDS8633
Canonical transcript exons
ENST00000240691 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00000821986 | 10809094 | 10810168 |
Expression profiles
Bgee: expression breadth tissue_specific, 5 present calls, max score 52.35.
Top tissues by expression
107 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 | 52.35 | silver quality |
| colonic epithelium | UBERON:0000397 | 42.45 | gold quality |
| cortical plate | UBERON:0005343 | 40.71 | silver quality |
| bone marrow cell | CL:0002092 | 38.21 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| calcaneal tendon | UBERON:0003701 | 35.57 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 35.06 | gold quality |
| bone marrow | UBERON:0002371 | 34.06 | gold quality |
| adrenal tissue | UBERON:0018303 | 33.42 | gold quality |
| muscle tissue | UBERON:0002385 | 32.30 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| corpus callosum | UBERON:0002336 | 32.01 | gold quality |
| monocyte | CL:0000576 | 31.68 | silver quality |
| leukocyte | CL:0000738 | 31.32 | silver quality |
| prefrontal cortex | UBERON:0000451 | 31.26 | gold quality |
| tonsil | UBERON:0002372 | 31.19 | gold quality |
| metanephros cortex | UBERON:0010533 | 30.92 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 30.28 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| vermiform appendix | UBERON:0001154 | 29.72 | gold quality |
| urinary bladder | UBERON:0001255 | 29.08 | gold quality |
| liver | UBERON:0002107 | 28.99 | gold quality |
| lymph node | UBERON:0000029 | 28.93 | gold quality |
| endometrium | UBERON:0001295 | 28.73 | silver quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| cortex of kidney | UBERON:0001225 | 27.72 | gold quality |
| right coronary artery | UBERON:0001625 | 27.72 | gold quality |
| frontal cortex | UBERON:0001870 | 27.34 | gold quality |
| blood | UBERON:0000178 | 27.04 | 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
Literature-anchored findings (GeneRIF, showing 2)
- A functionally compromised TAS2R receptor negatively impacts glucose homeostasis, providing an important link between alimentary chemosensation and metabolic disease. (PMID:19092995)
- genetic association studies in population of pregnant women in Czechoslovakia: Data suggest that an SNP in TAS2R9 (rs3741845) is associated with gestational diabetes; such genetic variation may play role in food preferences and compliance with healthy diet that may help prevent gestational diabetes. Associations were not found for SNPs in TAS1R2 and TAS2R7. (PMID:27757593)
Cross-species orthologs
0 orthologs
Paralogs (23): TAS2R8 (ENSG00000121314), TAS2R10 (ENSG00000121318), TAS2R7 (ENSG00000121377), TAS2R3 (ENSG00000127362), TAS2R4 (ENSG00000127364), TAS2R5 (ENSG00000127366), TAS2R16 (ENSG00000128519), TAS2R1 (ENSG00000169777), TAS2R60 (ENSG00000185899), TAS2R42 (ENSG00000186136), TAS2R19 (ENSG00000212124), TAS2R50 (ENSG00000212126), TAS2R14 (ENSG00000212127), TAS2R13 (ENSG00000212128), TAS2R41 (ENSG00000221855), TAS2R40 (ENSG00000221937), TAS2R46 (ENSG00000226761), TAS2R39 (ENSG00000236398), TAS2R43 (ENSG00000255374), TAS2R20 (ENSG00000255837), TAS2R30 (ENSG00000256188), TAS2R31 (ENSG00000256436), TAS2R38 (ENSG00000257138)
Protein
Protein identifiers
Taste receptor type 2 member 9 — Q9NYW1 (reviewed: Q9NYW1)
Alternative names: Taste receptor family B member 6
All UniProt accessions (1): Q9NYW1
UniProt curated annotations — full annotation on UniProt →
Function. Gustducin-coupled receptor implicated in the perception of bitter compounds in the oral cavity and the gastrointestinal tract. Signals through PLCB2 and the calcium-regulated cation channel TRPM5.
Subcellular location. Membrane.
Tissue specificity. Expressed in subsets of taste receptor cells of the tongue and palate epithelium and exclusively in gustducin-positive cells.
Miscellaneous. Several bitter taste receptors are expressed in a single taste receptor cell.
Similarity. Belongs to the G-protein coupled receptor T2R family.
RefSeq proteins (1): NP_076406* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR007960 | TAS2R | Family |
| IPR017452 | GPCR_Rhodpsn_7TM | Domain |
Pfam: PF05296
UniProt features (20 total): topological domain 8, transmembrane region 7, sequence variant 3, chain 1, glycosylation site 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q9NYW1-F1 | 82.59 | 0.44 |
Functional residue map
Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.
Glycosylation sites (1): 164
Function
Pathways and Gene Ontology
Reactome pathways
6 pathways
| ID | Pathway |
|---|---|
| R-HSA-418594 | G alpha (i) signalling events |
| R-HSA-420499 | Class C/3 (Metabotropic glutamate/pheromone receptors) |
| R-HSA-162582 | Signal Transduction |
| R-HSA-372790 | Signaling by GPCR |
| R-HSA-388396 | GPCR downstream signalling |
| R-HSA-500792 | GPCR ligand binding |
MSigDB gene sets: 39 (showing top):
GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, GOBP_DETECTION_OF_CHEMICAL_STIMULUS_INVOLVED_IN_SENSORY_PERCEPTION_OF_TASTE, GOBP_SENSORY_PERCEPTION_OF_TASTE, GOBP_DETECTION_OF_STIMULUS, GOBP_SENSORY_PERCEPTION, GOMF_TRANSMEMBRANE_SIGNALING_RECEPTOR_ACTIVITY, GOMF_BITTER_TASTE_RECEPTOR_ACTIVITY, GOMF_TASTE_RECEPTOR_ACTIVITY, GOMF_G_PROTEIN_COUPLED_RECEPTOR_ACTIVITY, GOBP_G_PROTEIN_COUPLED_RECEPTOR_SIGNALING_PATHWAY, GOBP_DETECTION_OF_STIMULUS_INVOLVED_IN_SENSORY_PERCEPTION, GOBP_SENSORY_PERCEPTION_OF_BITTER_TASTE, IL15_UP.V1_DN, IL21_UP.V1_DN, GSE13411_NAIVE_VS_IGM_MEMORY_BCELL_UP
GO Biological Process (4): detection of chemical stimulus involved in sensory perception of bitter taste (GO:0001580), signal transduction (GO:0007165), G protein-coupled receptor signaling pathway (GO:0007186), sensory perception of taste (GO:0050909)
GO Molecular Function (3): G protein-coupled receptor activity (GO:0004930), taste receptor activity (GO:0008527), bitter taste receptor activity (GO:0033038)
GO Cellular Component (2): plasma membrane (GO:0005886), membrane (GO:0016020)
Reactome top-level categories
Rollup of top-4 pathways:
| Category | Pathways |
|---|---|
| Signaling by GPCR | 2 |
| GPCR downstream signalling | 1 |
| GPCR ligand binding | 1 |
| Signal Transduction | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| detection of chemical stimulus involved in sensory perception of taste | 2 |
| transmembrane signaling receptor activity | 2 |
| sensory perception of bitter taste | 1 |
| 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 |
| G protein-coupled receptor signaling pathway | 1 |
| detection of chemical stimulus involved in sensory perception of bitter taste | 1 |
| taste receptor activity | 1 |
| membrane | 1 |
| cell periphery | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
234 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| TAS2R9 | GNAT3 | A8MTJ3 | 842 |
| TAS2R9 | MCHR2 | Q969V1 | 479 |
| TAS2R9 | TAS2R16 | Q9NYV7 | 473 |
| TAS2R9 | FFAR1 | O14842 | 462 |
| TAS2R9 | GPR32 | O75388 | 460 |
| TAS2R9 | FBXW12 | Q6X9E4 | 458 |
| TAS2R9 | NPFFR1 | Q9GZQ6 | 454 |
| TAS2R9 | GPR15 | P49685 | 444 |
| TAS2R9 | GNB3 | P16520 | 442 |
| TAS2R9 | SPDYE4 | A6NLX3 | 418 |
| TAS2R9 | CCL21 | O00585 | 414 |
| TAS2R9 | CALHM1 | Q8IU99 | 387 |
| TAS2R9 | PDE1A | P54750 | 371 |
| TAS2R9 | TAS2R46 | P59540 | 328 |
| TAS2R9 | GHSR | Q92847 | 308 |
IntAct
0 interactions, top by confidence:
ESM2 similar proteins: P59528, P59530, Q5Y4Z2, Q645T9, Q645U9, Q645V1, Q645Y5, Q645Z3, Q645Z5, Q646A7, Q646B6, Q646B8, Q646C6, Q646D2, Q646D8, Q646D9, Q646F7, Q646G3, Q646G5, Q675B7, Q675B8, Q675B9, Q675C0, Q67ER8, Q67ES1, Q67ES5, Q67ES6, Q67ES9, Q67ET3, Q67ET5, Q7M707, Q7M711, Q7M712, Q7M713, Q7M715, Q7M717, Q7M718, Q7M720, Q7M725, Q7RTR8
Diamond homologs: P0DSN6, P0DTE0, P59528, P59530, P59537, P59538, P59539, P59540, P59541, P59542, P59543, P59544, Q5Y4Y8, Q5Y4Y9, Q5Y4Z5, Q5Y4Z8, Q5Y500, Q645T0, Q645T2, Q645T3, Q645T4, Q645T6, Q645T7, Q645U8, Q645V1, Q645V2, Q645V3, Q645V4, Q645V6, Q645V7, Q645V8, Q645V9, Q645Z2, Q645Z5, Q645Z6, Q645Z7, Q645Z9, Q646A0, Q646A1, Q646A2
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
49 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 41 |
| Likely benign | 5 |
| Benign | 3 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
199 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 12:10809456:CTAA:C | acceptor_gain | 0.9600 |
| 12:10809460:C:CC | acceptor_gain | 0.9500 |
| 12:10809564:A:AC | donor_gain | 0.9400 |
| 12:10809565:C:CC | donor_gain | 0.9400 |
| 12:10809891:A:AC | donor_gain | 0.9200 |
| 12:10809457:TAA:T | acceptor_gain | 0.8900 |
| 12:10810056:G:A | donor_gain | 0.8300 |
| 12:10809565:CT:C | donor_gain | 0.8000 |
| 12:10809559:TACT:T | donor_loss | 0.7700 |
| 12:10809560:AC:A | donor_loss | 0.7700 |
| 12:10809561:C:CT | donor_loss | 0.7700 |
| 12:10809562:T:TA | donor_loss | 0.7700 |
| 12:10809563:CACT:C | donor_loss | 0.7700 |
| 12:10809564:A:T | donor_loss | 0.7700 |
| 12:10809896:A:T | donor_gain | 0.7500 |
| 12:10809565:CTTT:C | donor_gain | 0.7100 |
| 12:10809565:CTTTG:C | donor_gain | 0.7100 |
| 12:10810053:A:AC | donor_gain | 0.7000 |
| 12:10809765:C:CC | acceptor_gain | 0.6400 |
| 12:10809455:TCTAA:T | acceptor_gain | 0.6100 |
| 12:10809456:CTAAC:C | acceptor_gain | 0.6100 |
| 12:10809457:TAACT:T | acceptor_gain | 0.6100 |
| 12:10809458:AACTA:A | acceptor_gain | 0.6100 |
| 12:10809561:CTCA:C | donor_gain | 0.6100 |
| 12:10809458:AACT:A | acceptor_loss | 0.6000 |
| 12:10809459:AC:A | acceptor_loss | 0.6000 |
| 12:10809461:T:C | acceptor_loss | 0.6000 |
| 12:10809764:A:AC | acceptor_gain | 0.5900 |
| 12:10809459:ACTAG:A | acceptor_gain | 0.5700 |
| 12:10810103:A:AC | donor_gain | 0.5700 |
AlphaMissense
2067 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 12:10809788:A:C | S96R | 0.921 |
| 12:10809788:A:T | S96R | 0.921 |
| 12:10809790:T:G | S96R | 0.921 |
| 12:10809764:A:C | S104R | 0.919 |
| 12:10809764:A:T | S104R | 0.919 |
| 12:10809766:T:G | S104R | 0.919 |
| 12:10809998:G:C | F26L | 0.902 |
| 12:10809998:G:T | F26L | 0.902 |
| 12:10810000:A:G | F26L | 0.902 |
| 12:10809926:G:C | S50R | 0.886 |
| 12:10809926:G:T | S50R | 0.886 |
| 12:10809928:T:G | S50R | 0.886 |
| 12:10809911:T:A | R55S | 0.882 |
| 12:10809911:T:G | R55S | 0.882 |
| 12:10809365:A:C | F237L | 0.881 |
| 12:10809365:A:T | F237L | 0.881 |
| 12:10809367:A:G | F237L | 0.881 |
| 12:10810004:A:C | N24K | 0.867 |
| 12:10810004:A:T | N24K | 0.867 |
| 12:10809245:G:C | S277R | 0.859 |
| 12:10809245:G:T | S277R | 0.859 |
| 12:10809247:T:G | S277R | 0.859 |
| 12:10809784:A:G | W98R | 0.857 |
| 12:10809784:A:T | W98R | 0.857 |
| 12:10809772:A:G | C102R | 0.854 |
| 12:10809254:G:C | F274L | 0.848 |
| 12:10809254:G:T | F274L | 0.848 |
| 12:10809256:A:G | F274L | 0.848 |
| 12:10810018:C:G | G20R | 0.836 |
| 12:10810018:C:T | G20R | 0.836 |
dbSNP variants (sampled 300 via entrez): RS1000750425 (12:10809761 G>C), RS1002122124 (12:10808641 G>T), RS1003417834 (12:10811892 A>G), RS1006352063 (12:10809042 T>C,G), RS1008865307 (12:10810806 C>A), RS1009351943 (12:10811069 C>A,G,T), RS1009554445 (12:10812044 G>A,C), RS1011587786 (12:10810528 G>C), RS1012118717 (12:10810021 T>C,G), RS1012563631 (12:10810390 G>A), RS1013157279 (12:10809625 C>T), RS1013182123 (12:10811776 G>A), RS1013823703 (12:10809000 A>C,G), RS1014979544 (12:10810107 C>A,T), RS1015045747 (12:10811546 A>G)
Disease associations
OMIM: gene MIM:604795 | 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: yes
ChEMBL targets (1): CHEMBL3309110 (SINGLE PROTEIN)
Molecules with ChEMBL bioactivity
1 molecules (phase ≥1), by development phase (incl. off-target/promiscuous compounds). Patent mentions across the top 20 by phase: 40,234 (via chembl_molecule»patent_compound — counts attach to the compound, not the gene–compound relationship, so off-target/promiscuous molecules can dominate).
| Molecule | Name | Phase | Patents |
|---|---|---|---|
| CHEMBL434 | ISOPROTERENOL | 4 | 40,234 |
PharmGKB: 1 entry (VIP=true, CPIC=false)
GtoPdb / IUPHAR curated pharmacology
(IUPHAR/BPS Guide to Pharmacology — expert-curated)
Target class: gpcr — Taste 2 receptors
Most potent curated ligand interactions (3 total), top 3:
| Ligand | Action | Affinity | Parameter |
|---|---|---|---|
| ofloxacin | Agonist | 3.7 | pEC50 |
| pirenzepine | Agonist | 2.74 | pEC50 |
| procainamide | Agonist | 2.55 | pEC50 |
ChEMBL bioactivities
1 potent at pChembl≥5 of 1 total, top 1 by pChembl (potency: 10 = 0.1 nM, 6 = 1 µM).
| pChembl | Type | Value | Unit | Molecule |
|---|---|---|---|---|
| 8.31 | EC50 | 4.9 | nM | ISOPROTERENOL |
CTD chemical–gene interactions
5 total (human), top 5 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| propionaldehyde | decreases expression | 1 |
| CGP 52608 | affects binding, increases reaction | 1 |
| Benzo(a)pyrene | increases methylation | 1 |
| Aflatoxin B1 | decreases methylation | 1 |
| Asbestos, Crocidolite | affects expression | 1 |
ChEMBL screening assays
8 unique, capped per target: 7 functional, 1 binding
Representative assays (with source publication via chembl_document):
| Assay ID | Type | Description | Source paper |
|---|---|---|---|
| CHEMBL3361959 | Binding | Agonist activity at human TAS2R9 expressed in U2OS cells by Ga16gust44 Clone 7A FLIPR/summary (Abse5) assay | Identification of diarylsulfonamides as agonists of the free fatty acid receptor 4 (FFA4/GPR120). — Bioorg Med Chem Lett |
| CHEMBL4346428 | Functional | Antagonist activity at recombinant human TAS2R9 transiently expressed in HEK293T co-expressing Galpha16gust44 assessed as inhibition of ofloxacin-induced intracellular calcium level by measuring remaining activity at 25 uM by fluo-4AM dye b | Discovery and Development of S6821 and S7958 as Potent TAS2R8 Antagonists. — J Med Chem |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
- Targeted by drugs: Ofloxacin, Pirenzepine, Procainamide