FB2026_02 , released June 18, 2026
Gene: Dmel\TrpA1
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General Information
Symbol
Dmel\TrpA1
Species
D. melanogaster
Name
Transient receptor potential cation channel A1
Annotation Symbol
CG5751
Feature Type
FlyBase ID
FBgn0035934
Gene Model Status
Stock Availability
Gene Summary
Transient receptor potential cation channel A1 (TrpA1) encodes a cation channel activated by warming and by reactive chemicals. Its roles include the control of thermotaxis at innocuous temperatures, as well as thermal and chemical nociception in response to noxious heat and chemical exposure. [Date last reviewed: 2019-03-14] (FlyBase Gene Snapshot)
Also Known As

dTrpA1, dANKTM1, TrpA, Transient receptor potential A1, DmTRPA1

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
3-27
RefSeq locus
NT_037436 REGION:8894404..8905200
Sequence
Genomic Maps
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
Gene Ontology (GO) Annotations (34 terms)
Molecular Function (7 terms)
Terms Based on Experimental Evidence (5 terms)
CV Term
Evidence
References
Terms Based on Predictions or Assertions (2 terms)
CV Term
Evidence
References
Biological Process (24 terms)
Terms Based on Experimental Evidence (20 terms)
CV Term
Evidence
References
inferred from direct assay
inferred from direct assay
inferred from mutant phenotype
inferred from mutant phenotype
inferred from direct assay
inferred from mutant phenotype
inferred from direct assay
inferred from direct assay
inferred from direct assay
inferred from mutant phenotype
inferred from mutant phenotype
involved_in phototransduction
inferred from direct assay
involved_in response to heat
inferred from mutant phenotype
inferred from direct assay
inferred from mutant phenotype
inferred from mutant phenotype
involved_in thermotaxis
Terms Based on Predictions or Assertions (5 terms)
CV Term
Evidence
References
inferred from electronic annotation with InterPro:IPR005821
involved_in thermoception
inferred from biological aspect of ancestor with PANTHER:PTN008395498
inferred from electronic annotation with InterPro:IPR005821
Cellular Component (3 terms)
Terms Based on Experimental Evidence (2 terms)
CV Term
Evidence
References
inferred from direct assay
is_active_in plasma membrane
inferred from direct assay
Terms Based on Predictions or Assertions (2 terms)
CV Term
Evidence
References
located_in membrane
inferred by curator from GO:0005261
inferred from electronic annotation with InterPro:IPR005821
is_active_in plasma membrane
inferred from biological aspect of ancestor with PANTHER:PTN008395498
located_in plasma membrane
inferred from experiment
Protein Family (UniProt)
Belongs to the transient receptor (TC 1.A.4) family. (Q7Z020)
Summaries
Gene Snapshot
Transient receptor potential cation channel A1 (TrpA1) encodes a cation channel activated by warming and by reactive chemicals. Its roles include the control of thermotaxis at innocuous temperatures, as well as thermal and chemical nociception in response to noxious heat and chemical exposure. [Date last reviewed: 2019-03-14]
Gene Group (FlyBase)
TRANSIENT RECEPTOR POTENTIAL ION CHANNELS -
The Transient Receptor Potential (TRP) channel family are cation channels conserved from invertebrates to humans. TRP channels respond to diverse stimuli and are involved in a number of environmental sensory pathways. (Adapted from FBrf0220930 and FBrf0225477).
Protein Function (UniProtKB)
Essential for thermotaxis by sensing environmental temperature. Receptor-activated non-selective cation channel involved in detection of sensations such as temperature. Involved in heat nociception by being activated by warm temperature of about 24-29 degrees Celsius.
(UniProt, Q7Z020)
Summary (Interactive Fly)

heat-activated TRP family cation channel that is essential for thermotaxis - controls thermotaxis at innocuous temperatures, as well as thermal and chemical nociception in response to noxious heat and chemical exposure

Gene Model and Products
Number of Transcripts
5
Number of Unique Polypeptides
5

Please see the JBrowse view of Dmel\TrpA1 for information on other features

To submit a correction to a gene model please use the Contact FlyBase form

Protein Domains (via Pfam)
Isoform displayed:
Pfam protein domains
InterPro name
classification
start
end
Protein Domains (via SMART)
Isoform displayed:
SMART protein domains
InterPro name
classification
start
end
Structure
Protein 3D structure   (Predicted by AlphaFold)   (AlphaFold entry Q7Z020)

If you don't see a structure in the viewer, refresh your browser.
Model Confidence:
  • Very high (pLDDT > 90)
  • Confident (90 > pLDDT > 70)
  • Low (70 > pLDDT > 50)
  • Very low (pLDDT < 50)

AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.

Experimentally Determined Structures
Crossreferences
PDB - An information portal to biological macromolecular structures
Comments on Gene Model

Initial two exons previously annotated as final exons of one alternative transcript of CG5747 mfr. Species conservation data supporst the current gene structures.

Gene model reviewed during 5.45

Low-frequency RNA-Seq exon junction(s) not annotated.

Gene model reviewed during 5.55

Gene model reviewed during 6.32

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0331823
4573
1232
FBtr0331824
4570
1231
FBtr0331825
4259
1197
FBtr0331826
4256
1196
FBtr0331827
4462
1195
Additional Transcript Data and Comments
Reported size (kB)
Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
UniProt
RefSeq ID
GenBank
FBpp0304207
138.8
1232
7.67
FBpp0304208
139.1
1231
7.92
FBpp0304209
135.2
1197
7.84
FBpp0304210
135.4
1196
8.08
FBpp0304211
134.7
1195
7.68
Polypeptides with Identical Sequences

None of the polypeptides share 100% sequence identity.

Additional Polypeptide Data and Comments
Reported size (kDa)
Comments
External Data
Subunit Structure (UniProtKB)

Homotetramer.

(UniProt, Q7Z020)
Crossreferences
PDB - An information portal to biological macromolecular structures
Linkouts
Sequences Consistent with the Gene Model
Mapped Features

Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\TrpA1 using the Feature Mapper tool.

External Data
Crossreferences
Linkouts
Expression Data
Testis-specificity index

The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).

0.04

Transcript Expression
Additional Descriptive Data
Marker for
 
Subcellular Localization
CV Term
Polypeptide Expression
immunolocalization
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data

TrpA1 immunoreactivity was observed across most of the anterior midgut and in two lateral domains across middle midgut boundaries facing the anterior or posterior midgut. TrpA1-expressing cells were closely associated with immunoreactivity of the enteroendocrine cell nuclear marker, pros, but not with those of intestinal stem cell and enteroblast markers.

TrpA1 protein expression was observed in the mouthparts in neurons innervating sensilla numbers 8 and 9 of the labral sense organ.

TrpA1 is expressed in two uncharacterised groups of cells in the adult brain: the lateral cells (LC) and ventral cells (VC).

Marker for
 
Subcellular Localization
CV Term
Evidence
References
inferred from direct assay
is_active_in plasma membrane
inferred from direct assay
Expression Deduced from Reporters
Reporter: P{TrpA1-GAL4.C-D}
Stage
Tissue/Position (including subcellular localization)
Reference
Reporter: P{TrpA1-GAL4.R}
Stage
Tissue/Position (including subcellular localization)
Reference
Reporter: P{TrpA1-GAL4.SH}
Stage
Tissue/Position (including subcellular localization)
Reference
Reporter: P{TrpA1-QF.P}
Stage
Tissue/Position (including subcellular localization)
Reference
Reporter: PBac{TrpA1-GAL4.P}
Stage
Tissue/Position (including subcellular localization)
Reference
Stage
Tissue/Position (including subcellular localization)
Reference
Reporter: TI{GAL4}TrpA1-CD
Stage
Tissue/Position (including subcellular localization)
Reference
Stage
Tissue/Position (including subcellular localization)
Reference
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\TrpA1 in JBrowse
RNA-Seq by Region - Search RNA-Seq expression levels by exon or genomic region
Reference
See Gelbart and Emmert, 2013 for analysis details and data files for all genes.
Developmental Proteome: Life Cycle
Developmental Proteome: Embryogenesis
External Data and Images
Linkouts
DRscDB - A single-cell RNA-seq resource for data mining and data comparison across species
EMBL-EBI Single Cell Expression Atlas - Single cell expression across species
FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
FlyAtlas2 - A Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data
Flygut - An atlas of the Drosophila adult midgut
Images
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 49 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 62 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of TrpA1
Transgenic constructs containing regulatory region of TrpA1
Aberrations (Deficiencies and Duplications) ( 1 )
Inferred from experimentation ( 1 )
Inferred from location ( 6 )
Variants
Variant Molecular Consequences
Alleles Representing Disease-Implicated Variants
Phenotypes
For more details about a specific phenotype click on the relevant allele symbol.
Lethality
Allele
Other Phenotypes
Allele
Phenotype manifest in
Allele
Orthologs
Human Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Homo sapiens (Human) (42)
14 of 14
Yes
Yes
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
6  
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
6  
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1  
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
2  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
6  
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1  
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Rattus norvegicus (Norway rat) (39)
14 of 14
Yes
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Mus musculus (laboratory mouse) (39)
13 of 14
Yes
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Xenopus tropicalis (Western clawed frog) (21)
11 of 13
Yes
Yes
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
Danio rerio (Zebrafish) (40)
14 of 14
Yes
Yes
14 of 14
Yes
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Caenorhabditis elegans (Nematode, roundworm) (16)
9 of 14
Yes
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Anopheles gambiae (African malaria mosquito) (25)
12 of 12
Yes
Yes
1 of 12
No
No
Arabidopsis thaliana (thale-cress) (6)
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
Saccharomyces cerevisiae (Brewer's yeast) (5)
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
Schizosaccharomyces pombe (Fission yeast) (0)
Escherichia coli (enterobacterium) (2)
1 of 11
Yes
No
1 of 11
Yes
No
Other Organism Orthologs (via OrthoDB)
Data provided directly from OrthoDB:TrpA1. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Drosophila melanogaster (Fruit fly) (22)
5 of 13
3 of 13
2 of 13
2 of 13
2 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
Human Disease Associations
FlyBase Human Disease Model Reports
    Disease Ontology (DO) Annotations
    Models Based on Experimental Evidence ( 0 )
    Allele
    Disease
    Evidence
    References
    Potential Models Based on Orthology ( 1 )
    Modifiers Based on Experimental Evidence ( 2 )
    Disease Associations of Human Orthologs (via DIOPT v9.1 and OMIM)
    Note that ortholog calls supported by only 1 or 2 algorithms (DIOPT score < 3) are not shown.
    Functional Complementation Data
    Functional complementation data is computed by FlyBase using a combination of the orthology data obtained from DIOPT and OrthoDB and the allele-level genetic interaction data curated from the literature.
    Interactions
    Summary of Physical Interactions
    Interaction Browsers
    Summary of Genetic Interactions
    Interaction Browsers

    Please look at the allele data for full details of the genetic interactions
    Starting gene(s)
    Interaction type
    Interacting gene(s)
    Reference
    Starting gene(s)
    Interaction type
    Interacting gene(s)
    Reference
    External Data
    Subunit Structure (UniProtKB)
    Homotetramer.
    (UniProt, Q7Z020 )
    Linkouts
    DroID - A comprehensive database of gene and protein interactions.
    MIST (genetic) - An integrated Molecular Interaction Database
    Pathways
    Signaling Pathways (FlyBase)
    Metabolic Pathways
    FlyBase
    External Links
    External Data
    Linkouts
    Reactome - An open-source, open access, manually curated and peer-reviewed pathway database.
    SignaLink - A signaling pathway resource with multi-layered regulatory networks.
    Class of Gene
    Genomic Location and Detailed Mapping Data
    Chromosome (arm)
    3L
    Recombination map
    3-27
    Cytogenetic map
    Sequence location
    FlyBase Computed Cytological Location
    Cytogenetic map
    Evidence for location
    66E3-66E3
    Limits computationally determined from genome sequence between P{PZ}l(3)0162901629&P{PZ}mRpL1210534 and P{EP}Hsp26EP3336&P{EP}Hsp26EP3315
    Experimentally Determined Cytological Location
    Cytogenetic map
    Notes
    References
    Experimentally Determined Recombination Data
    Location
    Left of (cM)
    Right of (cM)
    Notes
    Stocks and Reagents
    Stocks (68)
    Genomic Clones (25)
    cDNA Clones (0)
     

    Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.

    cDNA clones, fully sequenced
    BDGP DGC clones
      Other clones
        Drosophila Genomics Resource Center cDNA clones

        For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.

          cDNA Clones, End Sequenced (ESTs)
          BDGP DGC clones
            Other clones
              RNAi and Array Information
              Linkouts
              DRSC - Results frm RNAi screens
              Antibody Information
              Laboratory Generated Antibodies
               
              Commercially Available Antibodies
               
              Cell Line Information
              Publicly Available Cell Lines
               
                Other Stable Cell Lines
                 
                  Other Comments

                  TrpA1 functions in temperature control of circadian rhythm in pacemaker neurons.

                  The isoform referred to as TRPA1(B) in FBrf0222493 is called "TRPA1-A" in FBrf0217493. The isoform referred to as TRPA1(A) in FBrf0222493 is similar to that called "TRPA1-D" in FBrf0217493, except that "TRPA1(A)" has an additional N-terminal amino acids.

                  The TRPA1(B) isoform encodes a non-selective cation channel that can be activated by heat, voltage and chemicals.

                  The "TRPA1(B)" isoform is activated by noxious chemicals when expressed in Xenopus oocytes and expression of this isoform can restore an avoidance response to noxious chemicals in TrpA1 mutant flies. However, the expression of this isoform inside the head should minimise its exposure to environmental irritants, and thus in wild-type flies its primary function may be as a warmth sensor.

                  The "TRPA1(A)" isoform is much less thermosensitive than TRPA1(B) when expressed in Xenopus oocytes and does not confer thermal sensitivity on neurons when expressed in them. Expression of this isoform can restore an avoidance response to noxious chemicals in TrpA1 mutant flies.

                  S2R+ cells expressing the "TRP1-A" isoform show heat-induced Ca[2+] responses.

                  S2R+ cells expressing the "TRPA1-B" isoform lack Ca[2+] responses to temperature in the 20-42[o]C range, but show Ca[2+] responses to an irritant chemical.

                  The "TRPA1-C" isoform rescues thermal nociception phenotypes when expressed in TrpA1 mutant nociceptors. S2R+ cells expressing this isoform do not show a meaningful response to temperatures in the range of 15-42[o]C, which suggests that "TRPA1-C" is not acting directly as a noxious heat sensor. S2R+ cells expressing this isoform do show Ca[2+] responses to an irritant chemical.

                  S2R+ cells expressing the "TRPA1-D" isoform show Ca[2+] responses significantly above the baseline beginning at a temperature of 34[o]C.

                  TrpA1 is required for thermal nociception in both larvae and adult flies.

                  TrpA1 is essential for class IV dendritic arborization neuron light responses.

                  TrpA1 is required cell autonomously for light transduction in class IV dendritic arborization neurons.

                  TrpA1 functions as a molecular sensor of warmth.

                  TrpA1 is required for normal thermotactic behaviour.

                  Larvae injected with dsRNA against TrpA1 show abnormal thermotactic behaviour, while their chemotactic response to n-octyl acetate and response to being touched with a hot (55oC) probe is normal.

                  The threshold for response of the "TRPA1(B)" isoform is 24-29[o]C.

                  Relationship to Other Genes
                  Source for database merge of
                  Additional comments
                  Nomenclature History
                  Source for database identify of

                  Source for identity of: TrpA1 Anktm1

                  Nomenclature comments
                  Etymology
                  Synonyms and Secondary IDs (30)
                  Reported As
                  Symbol Synonym
                  Anktm1
                  TrpA1
                  (Kubrak et al., 2026, Nallasivan et al., 2026, Berardi et al., 2025, Erginkaya et al., 2025, He et al., 2025, Hwang et al., 2025, Keesey et al., 2025, Krebs et al., 2025, Lehman et al., 2025, Matsunaga et al., 2025, Meng et al., 2025, Milleville et al., 2025, Sengupta et al., 2025, Shi et al., 2025, Singh et al., 2025, Song et al., 2025, Tadres et al., 2025, Yang et al., 2025, Bidros et al., 2024, Kubrak et al., 2024, Lowe et al., 2024, Luedke et al., 2024, Peng et al., 2024, Tleiss et al., 2024, Aalto et al., 2023, Bedont et al., 2023, Bonheur et al., 2023, Chen et al., 2023, De et al., 2023, Gong et al., 2023, Hao et al., 2023, Kurogi et al., 2023, Lee and Lim, 2023, Li et al., 2023, Mitchell et al., 2023, Miyashita et al., 2023, Petsakou and Perrimon, 2023, Song et al., 2023, Sun et al., 2023, Wu et al., 2023, Xu et al., 2023, Bai and Suzuki, 2022, Bajar et al., 2022, Gong et al., 2022, Gong et al., 2022, Kubrak et al., 2022, Lin et al., 2022, Schlichting et al., 2022, Suito et al., 2022, Chouhan et al., 2021, De and Chatterjee, 2021, Gowda et al., 2021, Hagen et al., 2021, Hsu et al., 2021, Jin et al., 2021, Kawamura et al., 2021, Kim et al., 2021, Landayan et al., 2021, Lee et al., 2021, Marguerite et al., 2021, Miao and Montell, 2021, Morris and Jasper, 2021, Prince et al., 2021, Yuan et al., 2021, Zhang et al., 2021, Zhang et al., 2021, Chen and Dahanukar, 2020, Fujisawa et al., 2020, Gu and Xiang, 2020.6.27, Hadjieconomou et al., 2020, Herrero et al., 2020, Hill et al., 2020, Huang et al., 2020, Li et al., 2020, Masuzzo et al., 2020, Morris et al., 2020, Öztürk-Çolak et al., 2020, Pop et al., 2020, Sato et al., 2020, Sudhakar et al., 2020, Vaccaro et al., 2020, Babski et al., 2019, FlyBase Genome Annotators, 2019-, Gu et al., 2019, Huang et al., 2019, Khuong et al., 2019, Ni et al., 2019, Xu et al., 2019, Zhang et al., 2019, Zhang et al., 2019, Aboudhiaf et al., 2018, Jang et al., 2018, Kim et al., 2018, Ly et al., 2018, Scheunemann et al., 2018, Shimell et al., 2018, Yadlapalli et al., 2018, Zhao et al., 2018, Allada et al., 2017, Artiushin and Sehgal, 2017, Aw et al., 2017, Chen et al., 2017, Fedina et al., 2017, Machado et al., 2017, Sitaraman et al., 2017, Tang et al., 2017, Zhang et al., 2017, Clandinin and Owens, 2016-, Clark et al., 2016, Du et al., 2016, Gene Disruption Project members, 2016-, Jayakumar et al., 2016, Ma et al., 2016, Sokabe et al., 2016, Soukup et al., 2016, Tong et al., 2016, Burn et al., 2015, Gene Disruption Project members, 2015-, Green et al., 2015, Head et al., 2015, Seidner et al., 2015, Bjordal et al., 2014, Boto et al., 2014, Doll and Broadie, 2014, Honda et al., 2014, Lin et al., 2014, Liu et al., 2014, Menuz et al., 2014, Rezával et al., 2014, Sun et al., 2014, Calcagno et al., 2013, Devineni et al., 2013, Flood et al., 2013, Flood et al., 2013, Gillespie and Hodge, 2013, Ni et al., 2013, Short and Lazzaro, 2013, Sivachenko et al., 2013, Vonhoff et al., 2013, Yamanaka et al., 2013, Zhang et al., 2013, Zhu, 2013, Bolukbasi et al., 2012, Kang et al., 2012, Kaun et al., 2012, Keleman et al., 2012, Lu et al., 2012, Majumdar et al., 2012, Plaçais et al., 2012, Rezaval et al., 2012, Talsma et al., 2012, Thistle et al., 2012, Tsubouchi et al., 2012, Yoshihara and Ito, 2012, Donlea et al., 2011, Kadowaki, 2011.10.7, Kadowaki, 2011.10.7, Neely et al., 2011, Shang et al., 2011, von Philipsborn et al., 2011, Alekseyenko et al., 2010, Kang et al., 2010, Kong et al., 2010, Xiang et al., 2010, Garrity, 2008.12.9, Kwon et al., 2008)
                  dTrpA1
                  (Gao et al., 2025, Ray et al., 2025, Tanaka et al., 2025, Yan et al., 2025, Brown et al., 2024, Comyn et al., 2024, Kim et al., 2024, Liu et al., 2024, Zhao et al., 2024, Han et al., 2022, Hobin et al., 2022, Honda, 2022, Hughson, 2022, Shao et al., 2022, Wang et al., 2022, Zhang et al., 2022, Coll-Tané et al., 2021, Dhawan et al., 2021, Gong et al., 2021, Guo et al., 2021, Lee and Adams, 2021, Zhang et al., 2021, Luan et al., 2020, Wu et al., 2020, Zhang et al., 2020, Bhukel et al., 2019, Dreyer et al., 2019, Hunt et al., 2019, Liu et al., 2019, Sangston and Hirsh, 2019, Feng et al., 2018, Kim et al., 2018, Pu et al., 2018, Ravi et al., 2018, Yamazaki et al., 2018, Hampel et al., 2017, Jang et al., 2017, Liu et al., 2017, Hoopfer, 2016, Liu et al., 2016, Pavlou et al., 2016, Soldano et al., 2016, Terada et al., 2016, Vienne et al., 2016, Hoopfer et al., 2015, Jang et al., 2015, Lee et al., 2015, Aso et al., 2014, Cavanaugh et al., 2014, Galili et al., 2014, Gorczyca et al., 2014, Guo et al., 2014, Honda et al., 2014, Inagaki et al., 2014, Laflamme et al., 2014, Schoofs et al., 2014, Schoofs et al., 2014, Yamamoto et al., 2014, Yang et al., 2014, Alekseyenko et al., 2013, Fan et al., 2013, Fujita et al., 2013, Jiang et al., 2013, McClure and Heberlein, 2013, Melom and Littleton, 2013, Perisse et al., 2013, Plaçais and Preat, 2013, Teodoro et al., 2013, Yamamoto et al., 2013, Zhang et al., 2013, Aso et al., 2012, Burke et al., 2012, Curran and Chalasani, 2012, Liu et al., 2012, Luo and Sehgal, 2012, Pan et al., 2012, Suver et al., 2012, Zhong et al., 2012, Cognigni et al., 2011, Pan et al., 2011, Alekseyenko et al., 2010, Carrillo et al., 2010, Certel et al., 2010, Keene et al., 2010, Krashes et al., 2009, Pulver et al., 2009, Hamada et al., 2008, Parisky et al., 2008, Shang et al., 2008, Hong et al., 2006, Rosenzweig et al., 2005, Rosenzweig et al., 2005)
                  Name Synonyms
                  Transient receptor potential A 1
                  Transient receptor potential cation channel
                  Transient receptor potential cation channel A1
                  Transient receptor potential cation channel A1 ortholog
                  transient receptor potential A1
                  transient-receptor-potential A1
                  Secondary FlyBase IDs
                    Datasets (0)
                    Study focus (0)
                    Experimental Role
                    Project
                    Project Type
                    Title
                    Study result (0)
                    Result
                    Result Type
                    Title
                    External Crossreferences and Linkouts ( 47 )
                    Sequence Crossreferences
                    NCBI Gene - Gene integrates information from a wide range of species. A record may include nomenclature, Reference Sequences (RefSeqs), maps, pathways, variations, phenotypes, and links to genome-, phenotype-, and locus-specific resources worldwide.
                    GenBank Nucleotide - A collection of sequences from several sources, including GenBank, RefSeq, TPA, and PDB.
                    GenBank Protein - A collection of sequences from several sources, including translations from annotated coding regions in GenBank, RefSeq and TPA, as well as records from SwissProt, PIR, PRF, and PDB.
                    RefSeq - A comprehensive, integrated, non-redundant, well-annotated set of reference sequences including genomic, transcript, and protein.
                    UniProt/GCRP - The gene-centric reference proteome (GCRP) provides a 1:1 mapping between genes and UniProt accessions in which a single 'canonical' isoform represents the product(s) of each protein-coding gene.
                    UniProt/Swiss-Prot - Manually annotated and reviewed records of protein sequence and functional information
                    UniProt/TrEMBL - Automatically annotated and unreviewed records of protein sequence and functional information
                    Other crossreferences
                    AlphaFold DB - AlphaFold provides open access to protein structure predictions for the human proteome and other key proteins of interest, to accelerate scientific research.
                    DRscDB - A single-cell RNA-seq resource for data mining and data comparison across species
                    EMBL-EBI Single Cell Expression Atlas - Single cell expression across species
                    FlyAtlas2 - A Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data
                    FlyMine - An integrated database for Drosophila genomics
                    KEGG Genes - Molecular building blocks of life in the genomic space.
                    MARRVEL_MODEL - MARRVEL (model organism gene)
                    PDB - An information portal to biological macromolecular structures
                    Linkouts
                    DroID - A comprehensive database of gene and protein interactions.
                    DRSC - Results frm RNAi screens
                    FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
                    FlyCyc Genes - Genes from a BioCyc PGDB for Dmel
                    Flygut - An atlas of the Drosophila adult midgut
                    FlyMet - A comprehensive tissue-specific metabolomics resource for Drosophila.
                    iBeetle-Base - RNAi phenotypes in the red flour beetle (Tribolium castaneum)
                    Interactive Fly - A cyberspace guide to Drosophila development and metazoan evolution
                    MIST (genetic) - An integrated Molecular Interaction Database
                    Reactome - An open-source, open access, manually curated and peer-reviewed pathway database.
                    SignaLink - A signaling pathway resource with multi-layered regulatory networks.
                    References (748)