TAS2R30
gene geneOn this page
Also known as T2R30
Summary
TAS2R30 (taste 2 receptor member 30, HGNC:19112) is a protein-coding gene on chromosome 12p13.2, encoding Taste receptor type 2 member 30 (P59541). Receptor that may play a role in the perception of bitterness and is gustducin-linked.
Enables bitter taste receptor activity. Involved in detection of chemical stimulus involved in sensory perception of bitter taste. Predicted to be located in plasma membrane. Predicted to be active in membrane.
Source: NCBI Gene 259293 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 2 total
- Druggable target: yes — 1 molecules with ChEMBL bioactivity
- MANE Select transcript:
NM_001097643
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:19112 |
| Approved symbol | TAS2R30 |
| Name | taste 2 receptor member 30 |
| Location | 12p13.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | T2R30 |
| Ensembl gene | ENSG00000256188 |
| Ensembl biotype | protein_coding |
| OMIM | 613963 |
| Entrez | 259293 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000539585
RefSeq mRNA: 1 — MANE Select: NM_001097643
NM_001097643
CCDS: CCDS53750
Canonical transcript exons
ENST00000539585 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001750591 | 11132958 | 11134644 |
Expression profiles
Bgee: expression breadth ubiquitous, 124 present calls, max score 79.40.
Top tissues by expression
129 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| corpus callosum | UBERON:0002336 | 79.40 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 78.87 | gold quality |
| adrenal tissue | UBERON:0018303 | 77.46 | gold quality |
| calcaneal tendon | UBERON:0003701 | 76.89 | gold quality |
| bone marrow cell | CL:0002092 | 74.06 | silver quality |
| sural nerve | UBERON:0015488 | 71.71 | gold quality |
| colonic epithelium | UBERON:0000397 | 69.64 | gold quality |
| tonsil | UBERON:0002372 | 66.17 | gold quality |
| bone marrow | UBERON:0002371 | 61.89 | silver quality |
| hindlimb stylopod muscle | UBERON:0004252 | 56.24 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 55.72 | gold quality |
| ventricular zone | UBERON:0003053 | 54.19 | gold quality |
| endometrium | UBERON:0001295 | 53.12 | gold quality |
| muscle tissue | UBERON:0002385 | 52.07 | gold quality |
| monocyte | CL:0000576 | 51.88 | gold quality |
| urinary bladder | UBERON:0001255 | 51.24 | gold quality |
| stromal cell of endometrium | CL:0002255 | 50.48 | silver quality |
| leukocyte | CL:0000738 | 50.42 | gold quality |
| ovary | UBERON:0000992 | 50.15 | gold quality |
| left ovary | UBERON:0002119 | 49.10 | gold quality |
| liver | UBERON:0002107 | 48.89 | gold quality |
| ganglionic eminence | UBERON:0004023 | 48.51 | silver quality |
| uterine cervix | UBERON:0000002 | 48.29 | gold quality |
| kidney | UBERON:0002113 | 47.84 | gold quality |
| right ovary | UBERON:0002118 | 47.63 | gold quality |
| lung | UBERON:0002048 | 47.44 | gold quality |
| cerebellar cortex | UBERON:0002129 | 47.34 | silver quality |
| cerebellum | UBERON:0002037 | 47.17 | silver quality |
| superior frontal gyrus | UBERON:0002661 | 47.10 | silver quality |
| cerebellar hemisphere | UBERON:0002245 | 47.06 | silver quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.05 |
Regulation
Is transcription factor: no
Cross-species orthologs
4 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Tas2r136 | ENSMUSG00000053217 |
| mus_musculus | Tas2r120 | ENSMUSG00000059382 |
| rattus_norvegicus | Tas2r120 | ENSRNOG00000021445 |
| rattus_norvegicus | Tas2r136 | ENSRNOG00000029561 |
Paralogs (23): TAS2R8 (ENSG00000121314), TAS2R10 (ENSG00000121318), TAS2R7 (ENSG00000121377), TAS2R9 (ENSG00000121381), 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), TAS2R31 (ENSG00000256436), TAS2R38 (ENSG00000257138)
Protein
Protein identifiers
Taste receptor type 2 member 30 — P59541 (reviewed: P59541)
Alternative names: Taste receptor type 2 member 47
All UniProt accessions (1): P59541
UniProt curated annotations — full annotation on UniProt →
Function. Receptor that may play a role in the perception of bitterness and is gustducin-linked. May play a role in sensing the chemical composition of the gastrointestinal content. The activity of this receptor may stimulate alpha gustducin, mediate PLC-beta-2 activation and lead to the gating of TRPM5.
Subcellular location. Membrane.
Tissue specificity. Expressed in subsets of taste receptor cells of the tongue and exclusively in gustducin-positive cells.
Miscellaneous. Most taste cells may be activated by a limited number of bitter compounds; individual taste cells can discriminate among bitter stimuli.
Similarity. Belongs to the G-protein coupled receptor T2R family.
RefSeq proteins (1): NP_001091112* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR007960 | TAS2R | Family |
Pfam: PF05296
UniProt features (20 total): topological domain 8, transmembrane region 7, glycosylation site 2, chain 1, sequence variant 1, sequence conflict 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-P59541-F1 | 85.23 | 0.51 |
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 (2): 161, 176
Function
Pathways and Gene Ontology
Reactome pathways
9 pathways
| ID | Pathway |
|---|---|
| R-HSA-418594 | G alpha (i) signalling events |
| R-HSA-420499 | Class C/3 (Metabotropic glutamate/pheromone receptors) |
| R-HSA-9717207 | Sensory perception of sweet, bitter, and umami (glutamate) taste |
| R-HSA-162582 | Signal Transduction |
| R-HSA-372790 | Signaling by GPCR |
| R-HSA-388396 | GPCR downstream signalling |
| R-HSA-500792 | GPCR ligand binding |
| R-HSA-9709957 | Sensory Perception |
| R-HSA-9717189 | Sensory perception of taste |
MSigDB gene sets: 25 (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, ZIM3_TARGET_GENES, DESCARTES_MAIN_FETAL_PDE1C_ACSM3_POSITIVE_CELLS, OSMAN_BLOOD_CHAD63_KH_AGE_18_50YO_HIGH_DOSE_SUBJECTS_24HR_DN
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 (2): G protein-coupled receptor activity (GO:0004930), bitter taste receptor activity (GO:0033038)
GO Cellular Component (2): plasma membrane (GO:0005886), membrane (GO:0016020)
Reactome top-level categories
Rollup of top-6 pathways:
| Category | Pathways |
|---|---|
| Signaling by GPCR | 2 |
| GPCR downstream signalling | 1 |
| GPCR ligand binding | 1 |
| Sensory perception of taste | 1 |
| Signal Transduction | 1 |
| Sensory Perception | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| detection of chemical stimulus involved in sensory perception of taste | 1 |
| 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 |
| transmembrane signaling receptor activity | 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
214 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| TAS2R30 | TAS1R2 | Q8TE23 | 447 |
| TAS2R30 | GNAT3 | A8MTJ3 | 446 |
| TAS2R30 | TAS1R3 | Q7RTX0 | 430 |
| TAS2R30 | ZNF701 | Q9NV72 | 404 |
| TAS2R30 | TRPM5 | Q9NZQ8 | 400 |
| TAS2R30 | PLCB2 | Q00722 | 397 |
| TAS2R30 | CYB561D1 | Q8N8Q1 | 348 |
| TAS2R30 | OR8U1 | Q8NH10 | 327 |
| TAS2R30 | HRCT1 | Q6UXD1 | 324 |
| TAS2R30 | DNHD1 | Q96M86 | 305 |
| TAS2R30 | TOP6BL | Q8N6T0 | 300 |
| TAS2R30 | KIAA0040 | Q15053 | 298 |
| TAS2R30 | TAS1R1 | Q7RTX1 | 290 |
| TAS2R30 | TAS2R4 | Q9NYW5 | 281 |
| TAS2R30 | BCAS4 | Q8TDM0 | 278 |
IntAct
0 interactions, top by confidence:
ESM2 similar proteins: P0DSN6, P0DTE0, P59537, P59538, P59539, P59540, P59541, P59542, P59543, P59544, Q5Y4Y8, Q5Y4Y9, Q5Y4Z5, Q5Y4Z8, Q5Y500, Q645T2, Q645T3, Q645T4, Q645T6, Q645V2, Q645V3, Q645V4, Q645V6, Q645V7, Q645Z2, Q645Z6, Q645Z7, Q645Z9, Q646A0, Q646A1, Q646B4, Q646B9, Q646C0, Q646C1, Q646C2, Q646C3, Q646E0, Q646E1, Q646E2, Q646E3
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
2 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 2 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
180 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 12:11133637:C:CT | acceptor_gain | 0.8700 |
| 12:11133634:T:TC | acceptor_gain | 0.8600 |
| 12:11133639:C:CT | acceptor_gain | 0.8600 |
| 12:11133267:C:CT | donor_gain | 0.8500 |
| 12:11133634:T:C | acceptor_gain | 0.8100 |
| 12:11133640:A:T | acceptor_gain | 0.8000 |
| 12:11133807:C:CT | acceptor_gain | 0.7700 |
| 12:11134590:T:TA | donor_gain | 0.7700 |
| 12:11133650:T:TC | acceptor_gain | 0.7300 |
| 12:11133268:C:CT | donor_gain | 0.7200 |
| 12:11133655:A:T | acceptor_gain | 0.6900 |
| 12:11133630:A:C | acceptor_gain | 0.6400 |
| 12:11133825:C:CT | acceptor_gain | 0.6400 |
| 12:11133265:CA:C | donor_gain | 0.6200 |
| 12:11133883:A:C | acceptor_gain | 0.6200 |
| 12:11134591:C:A | donor_gain | 0.6100 |
| 12:11133658:A:T | acceptor_gain | 0.6000 |
| 12:11133826:A:T | acceptor_gain | 0.6000 |
| 12:11133646:C:CT | acceptor_gain | 0.5800 |
| 12:11133657:C:CT | acceptor_gain | 0.5700 |
| 12:11133799:A:C | acceptor_gain | 0.5700 |
| 12:11134541:TGAA:T | donor_gain | 0.5700 |
| 12:11133809:C:CT | acceptor_gain | 0.5600 |
| 12:11133810:A:T | acceptor_gain | 0.5100 |
| 12:11134608:T:A | donor_gain | 0.5100 |
| 12:11133630:A:AC | acceptor_gain | 0.5000 |
| 12:11133266:AC:A | donor_gain | 0.4800 |
| 12:11133798:CA:C | acceptor_gain | 0.4700 |
| 12:11133879:CTTTA:C | acceptor_gain | 0.4700 |
| 12:11133880:TTTAT:T | acceptor_gain | 0.4700 |
AlphaMissense
2104 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 12:11133891:A:C | F118L | 0.867 |
| 12:11133891:A:T | F118L | 0.867 |
| 12:11133893:A:G | F118L | 0.867 |
| 12:11133543:A:C | F234L | 0.838 |
| 12:11133543:A:T | F234L | 0.838 |
| 12:11133545:A:G | F234L | 0.838 |
| 12:11133960:G:C | S95R | 0.828 |
| 12:11133960:G:T | S95R | 0.828 |
| 12:11133962:T:G | S95R | 0.828 |
| 12:11134167:G:C | F26L | 0.827 |
| 12:11134167:G:T | F26L | 0.827 |
| 12:11134169:A:G | F26L | 0.827 |
| 12:11133906:G:C | F113L | 0.820 |
| 12:11133906:G:T | F113L | 0.820 |
| 12:11133908:A:G | F113L | 0.820 |
| 12:11133942:G:C | S101R | 0.812 |
| 12:11133942:G:T | S101R | 0.812 |
| 12:11133944:T:G | S101R | 0.812 |
| 12:11133936:G:C | S103R | 0.806 |
| 12:11133936:G:T | S103R | 0.806 |
| 12:11133938:T:G | S103R | 0.806 |
| 12:11134067:A:G | W60R | 0.757 |
| 12:11134067:A:T | W60R | 0.757 |
| 12:11133435:G:C | S270R | 0.755 |
| 12:11133435:G:T | S270R | 0.755 |
| 12:11133437:T:G | S270R | 0.755 |
| 12:11134194:A:C | F17L | 0.752 |
| 12:11134194:A:T | F17L | 0.752 |
| 12:11134196:A:G | F17L | 0.752 |
| 12:11133930:A:C | F105L | 0.731 |
dbSNP variants (sampled 300 via entrez): RS1001020686 (12:11135645 C>T), RS1001066686 (12:11136120 T>C), RS1002078715 (12:11134563 T>C), RS1005023446 (12:11133627 G>C), RS1007616130 (12:11135015 C>T), RS1008156114 (12:11132995 A>G), RS1008268950 (12:11132655 G>A,C), RS1011780027 (12:11133016 AT>A), RS1012075587 (12:11133284 G>T), RS1012408626 (12:11136475 C>A,T), RS1012902574 (12:11135627 G>A), RS1013410099 (12:11134853 T>C), RS1013513178 (12:11134611 T>C), RS1015896328 (12:11134621 T>C,G), RS1017615402 (12:11135023 C>T)
Disease associations
OMIM: gene MIM:613963 | 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): CHEMBL4523254 (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 |
|---|---|---|---|
| denatonium | Agonist | 6.57 | pEC50 |
| absinthin | Agonist | 6.4 | pEC50 |
| amarogentin | Agonist | 6.39 | 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
8 total (human), top 8 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| 2-methyl-4-isothiazolin-3-one | decreases expression | 1 |
| pentanal | decreases expression | 1 |
| Sunitinib | decreases expression | 1 |
| Benzo(a)pyrene | increases methylation | 1 |
| Cadmium | increases abundance, increases expression | 1 |
| Valproic Acid | decreases methylation | 1 |
| Aflatoxin B1 | decreases methylation | 1 |
| Cadmium Chloride | increases abundance, increases expression | 1 |
ChEMBL screening assays
7 unique, capped per target: 7 functional
Representative assays (with source publication via chembl_document):
| Assay ID | Type | Description | Source paper |
|---|---|---|---|
| CHEMBL4346432 | Functional | Antagonist activity at recombinant human TAS2R30 transiently expressed in HEK293T co-expressing Galpha16gust44 assessed as inhibition of denatonium-induced intracellular calcium level by measuring remaining activity at 25 uM by fluo-4AM dye | 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
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.