FB2026_03 , released September 17, 2026
Gene: Dmel\DptA
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General Information
Symbol
Dmel\DptA
Species
D. melanogaster
Name
Diptericin A
Annotation Symbol
CG12763
Feature Type
FlyBase ID
FBgn0004240
Gene Model Status
Stock Availability
Gene Summary
Diptericin A (DptA) encodes an immune inducible antibacterial peptide with activity against Gram-negative bacteria. It is expressed in the fat body during the systemic immune response and in various epithelia. Its expression is regulated at the transcriptional level by the immune deficiency pathway. [Date last reviewed: 2019-03-07] (FlyBase Gene Snapshot)
Also Known As

Diptericin, Dpt, Dipt, Dip, DiptA

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
2-86
RefSeq locus
NT_033778 REGION:18865765..18866260
Sequence
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
Gene Ontology (GO) Annotations (6 terms)
Molecular Function (0 terms)
Terms Based on Experimental Evidence (0 terms)
Terms Based on Predictions or Assertions (0 terms)
Biological Process (6 terms)
Terms Based on Experimental Evidence (5 terms)
CV Term
Evidence
References
inferred from expression pattern
inferred from direct assay
inferred from high throughput mutant phenotype
inferred from expression pattern
inferred from high throughput mutant phenotype
inferred from high throughput expression pattern
inferred from direct assay
inferred from mutant phenotype
Terms Based on Predictions or Assertions (1 term)
CV Term
Evidence
References
inferred from sequence or structural similarity
Cellular Component (0 terms)
Terms Based on Experimental Evidence (0 terms)
Terms Based on Predictions or Assertions (0 terms)
Gene Group / Complex (FlyBase)
Protein Family (UniProt)
Belongs to the attacin/sarcotoxin-2 family. (P24492)
Protein Signatures (InterPro)
Summaries
Gene Snapshot
Diptericin A (DptA) encodes an immune inducible antibacterial peptide with activity against Gram-negative bacteria. It is expressed in the fat body during the systemic immune response and in various epithelia. Its expression is regulated at the transcriptional level by the immune deficiency pathway. [Date last reviewed: 2019-03-07]
Gene Group / Complex (FlyBase)
DIPTERICINS -
Diptericins are antimicrobial peptides induced by the immune deficiency (Imd) signaling pathway. (Adapted from FBrf0263699.)
Protein Function (UniProtKB)
Antimicrobial peptide required to resist Gram-negative bacterial infections, regulated by Dredd.
(UniProt, P24492)
Gene Model and Products
Number of Transcripts
1
Number of Unique Polypeptides
1

Please see the JBrowse view of Dmel\DptA 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 P24492)

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
Comments on Gene Model

Gene model reviewed during 5.50

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0086620
496
106
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
FBpp0085802
11.3
106
6.77
Polypeptides with Identical Sequences

There is only one protein coding transcript and one polypeptide associated with this gene

Additional Polypeptide Data and Comments
Reported size (kDa)

106 (aa); 9 (kD predicted)

Comments
External Data
Crossreferences
InterPro - A database of protein families, domains and functional sites
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\DptA using the Feature Mapper tool.

External Data
Crossreferences
Eukaryotic Promoter Database - A collection of databases of experimentally validated promoters for selected model organisms.
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).

-0.63

Transcript Expression
Additional Descriptive Data

Dpt transcripts are expressed in response to inoculation with a bacterial suspension. They are detected in adult males 2 hours after inoculation and reach a peak at 4 hours after inoculation. A similar response was observed in larvae and late pupae. A low level of Dpt transcripts was observed in untreated pupae and adults.

Marker for
 
Subcellular Localization
CV Term
Polypeptide Expression
Additional Descriptive Data
Marker for
 
Subcellular Localization
CV Term
Evidence
References
Expression Deduced from Reporters
Reporter: P{Dipt2.2-lacZ}
Stage
Tissue/Position (including subcellular localization)
Reference
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\DptA 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
BDGP expression data - Patterns of gene expression in Drosophila embryogenesis
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
Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
Images
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 12 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 12 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of DptA
Transgenic constructs containing regulatory region of DptA
Aberrations (Deficiencies and Duplications) ( 2 )
Inferred from experimentation ( 2 )
Inferred from location ( 5 )
Variants
Variant Molecular Consequences
Alleles Representing Disease-Implicated Variants
Phenotypes
Orthologs
Human Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Homo sapiens (Human) (0)
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Rattus norvegicus (Norway rat) (0)
Mus musculus (laboratory mouse) (0)
Xenopus tropicalis (Western clawed frog) (0)
Danio rerio (Zebrafish) (0)
Caenorhabditis elegans (Nematode, roundworm) (0)
Anopheles gambiae (African malaria mosquito) (0)
Arabidopsis thaliana (thale-cress) (0)
Saccharomyces cerevisiae (Brewer's yeast) (0)
Schizosaccharomyces pombe (Fission yeast) (0)
Escherichia coli (enterobacterium) (0)
Other Organism Orthologs (via OrthoDB)
Data provided directly from OrthoDB:DptA. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Drosophila melanogaster (Fruit fly) (3)
3 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 ( 0 )
    Human Ortholog
    Disease
    Evidence
    References
    Modifiers Based on Experimental Evidence ( 3 )
    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.
    Homo sapiens (Human)
    Gene name
    Score
    OMIM
    OMIM Phenotype
    DO term
    Complementation?
    Transgene?
    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
    Summary of Genetic Interactions
    Interaction Browsers
    Starting gene(s)
    Interaction type
    Interacting gene(s)
    Reference
    Starting gene(s)
    Interaction type
    Interacting gene(s)
    Reference
    External Data
    Linkouts
    DroID - A comprehensive database of gene and protein interactions.
    Pathways
    Signaling Pathways (FlyBase)
    Metabolic Pathways
    FlyBase
    External Links
    External Data
    Linkouts
    KEGG Pathways - A collection of manually drawn pathway maps representing knowledge of molecular interaction, reaction and relation networks.
    Class of Gene
    Genomic Location and Detailed Mapping Data
    Chromosome (arm)
    2R
    Recombination map
    2-86
    Cytogenetic map
    Sequence location
    FlyBase Computed Cytological Location
    Cytogenetic map
    Evidence for location
    55F8-55F8
    Limits computationally determined from genome sequence between P{PZ}l(2)0370903709 and P{lacW}prodk08810
    Experimentally Determined Cytological Location
    Cytogenetic map
    Notes
    References
    56A-56A
    (determined by in situ hybridisation)
    Experimentally Determined Recombination Data
    Location
    Left of (cM)
    Right of (cM)
    Notes
    Stocks and Reagents
    Stocks (16)
    Genomic Clones (19)
    cDNA Clones (19)
     

    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)
    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

        Identified as a gene with significant level of mRNA cycling as assessed by expression analysis using high density oligonucleotide arrays with probe generated from adult heads harvested over six time points over the course of a day. Shows alteration in expression in a Clk mutant background.

        In a sample of 79 genes with multiple introns, 33 showed significant heterogeneity in G+C content among introns of the same gene and significant positive correspondence between the intron and the third codon position G+C content within genes. These results are consistent with selection adding against preferred codons at the start of genes.

        Ecol\lacZDpt.PR adults are pricked with a sterile needle dipped in culture pellets of various living microorganisms (distinct bacterial strains, fungal spores or hyphae). Pricking results in a low but clearly detectable expression of all antimicrobial genes and these genes are induced above the background level by specific classes of microorganism.

        Antibacterial genes are not induced in L.boulardi resistant strains of Drosophila suggesting they cannot be involved directly in the antiparasitoid response.

        The κB motifs of Dpt and CecA1 are not functionally equivalent. Mutants carrying no copies of dl and a single copy of Dif retain their full capacity to express the Dpt and CecA1 genes in response to bacterial challenge.

        Genes encoding antibacterial peptides are regulated in a manner distinct from that of Drs, encoding the antifungal peptide.

        The response to Dipt::lacZ reporter constructs to bacterial challenge is ecdysteroid-dependent, being much reduced on a ecd1 or dor mutant background.

        The increase, or maturation, of Dpt promoter activity during the third larval instar in response to bacterial challenge is ecdysteroid- dependent, as demonstrated using wild type and ecd1 or dor22 mutant larvae.

        Transcription is not strongly induced by hymenopteran parasitoids.

        A 45kD protein that binds sequence-specifically to the Dpt promoter GAAANN motif in fat body and blood cell extracts has been identified.

        Ecol\lacZ reporter gene constructs demonstrate that a 2.2kb upstream sequence can only confer full bacterial inducibility when it carries both 17bp motifs in the proximal promoter region.

        Analysis of the Dpt promoter defined two 17bp repeats essential for LPS inducibility. Addition of extra copies of the 17bp repeat increases the level of transcription on LPS induction. A specific DNA-protein binding activity present only in induced blood cells and fat body suggests an induction mechanism similar to that of mammalian NF-κB.

        Dpt shows at least 4 distinct expression phases: young larvae, late third instar larvae, pupae and adults. The complexity may be related to the presence of multiple copies of response elements in the Dpt upstream sequences.

        Isolated from a cDNA library using probes complementary to residues 38-43 of Phormia diptericin A.

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

        Source for identity of: DptA Dpt

        Nomenclature comments
        Etymology
        Synonyms and Secondary IDs (35)
        Reported As
        Symbol Synonym
        Dipt
        (Hajji et al., 2026, Sarkar et al., 2026, Castelló-Sanjuán et al., 2025, Kim et al., 2024, Luo et al., 2024, Loudhaief et al., 2023, Odnokoz et al., 2023, Delventhal et al., 2022, De Groef et al., 2021, Harsh et al., 2020, Martínez et al., 2020, Belmonte et al., 2019, Molaei et al., 2019, Yang et al., 2019, Badinloo et al., 2018, Min and Tatar, 2018, Kurz et al., 2017, Odnokoz et al., 2017, Allen et al., 2016, Helenius et al., 2016, Shen et al., 2016, Li and Dijkers, 2015, Sudmeier et al., 2015, Wu et al., 2015, Dantoft et al., 2013, Radyuk et al., 2013, Jones et al., 2012, Nakamoto et al., 2012, Petersen et al., 2012, Akhouayri et al., 2011, Clark et al., 2011, Esfahani and Engström, 2011, Walker et al., 2011, Aymeric et al., 2010, Paquette et al., 2010, Radyuk et al., 2010, Yagi et al., 2010, Thevenon et al., 2009, Bergeret et al., 2008, Maillet et al., 2008, Vonkavaara et al., 2008, Dijkers and O'Farrell, 2007, Bischoff et al., 2006, Jang et al., 2006, Leulier et al., 2006, Apidianakis et al., 2005, Johansson et al., 2005, Zambon et al., 2005, Hay et al., 2004, Landis et al., 2004, Naitza et al., 2002, Boulanger et al., 2001, Lindmark et al., 2001, Benassi et al., 2000, Hita et al., 1999, Braun et al., 1998, Nicolas et al., 1998, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Clark, 1997.8.12, Lemaitre et al., 1997, Lemaitre et al., 1996, Meister et al., 1994)
        Dpt
        (Wang et al., 2026, Wang et al., 2026, Duan et al., 2025, Qin et al., 2025, Uliczka et al., 2025, Wang et al., 2025, Wu et al., 2025, Yang et al., 2025, Zheng et al., 2025, Huang et al., 2024, Hu et al., 2024, Kim et al., 2024, Li et al., 2024, Polunina et al., 2024, Gupta et al., 2023, He et al., 2023, Lassetter et al., 2023, Loudhaief et al., 2023, Pan et al., 2023, Wang et al., 2023, Yao et al., 2023, Chen et al., 2022, Lu and Chtarbanova, 2022, Shen et al., 2022, Zhou et al., 2022, Kanoh et al., 2021, Ramond et al., 2021, Wang et al., 2021, Watson et al., 2021, Zhou et al., 2021, Kosakamoto et al., 2020, Lin et al., 2020, Nonaka et al., 2020, Sharma et al., 2020, Yuan et al., 2020, Yurkevych et al., 2020, Zhang et al., 2020, Araki et al., 2019, Chowdhury et al., 2019, Hanson et al., 2019, Hanson et al., 2019, Kano and Yagi, 2019, Kopp and Park, 2019, Singh and Tapadia, 2019, Troha et al., 2019, Abhyankar et al., 2018, Barajas-Azpeleta et al., 2018, Troha et al., 2018, Ueda et al., 2018, Bozler et al., 2017, Dostálová et al., 2017, Kim et al., 2017, Wang et al., 2017, Costechareyre et al., 2016, Guillou et al., 2016, Liu et al., 2016, Neyen et al., 2016, Piegholdt et al., 2016, Sekihara et al., 2016, Unckless et al., 2016, Zhou et al., 2016, Beebe et al., 2015, Dudzic et al., 2015, Fan et al., 2015, Jones et al., 2015, Kanoh et al., 2015, Momiuchi et al., 2015, Xia et al., 2015, Yamamoto-Hino et al., 2015, Chen et al., 2014, Engel et al., 2014, Guo et al., 2014, Haller et al., 2014, Ruiz et al., 2014, Stronach et al., 2014, Varma et al., 2014, Zhu et al., 2014, Aparicio et al., 2013, Clark et al., 2013, Durdevic et al., 2013, Favrin et al., 2013, Gendrin et al., 2013, Short and Lazzaro, 2013, Yagi et al., 2013, An et al., 2012, Bosco-Drayon et al., 2012, Chakrabarti et al., 2012, Choi and Hyun, 2012, Kalajdzic et al., 2012, Marek and Kagan, 2012, Neyen et al., 2012, Rera et al., 2012, Tsuzuki et al., 2012, Wu et al., 2012, Fullaondo et al., 2011, Kikuchi et al., 2011, Zaidman-Rémy et al., 2011, Zhao and Haddad, 2011, Becker et al., 2010, Buchon et al., 2010, Zhao et al., 2010, Buchon et al., 2009, Charroux and Royet, 2009, Cronin et al., 2009, Ha et al., 2009, Sackton and Clark, 2009, Wei et al., 2009, Wiklund et al., 2009, Zhang and Palli, 2009, Aggarwal et al., 2008, Deddouche et al., 2008, Flatt et al., 2008, Jin et al., 2008, Lhocine et al., 2008, Libert et al., 2008, Linder et al., 2008, Reed et al., 2008, Ryu et al., 2008, Scherfer et al., 2008, Sekiya et al., 2008, Tang et al., 2008, Wigby et al., 2008, Domanitskaya et al., 2007, Harari-Steinberg et al., 2007, Reiter et al., 2007, Brun et al., 2006, Kaneko et al., 2006, Scherfer et al., 2006, Tang et al., 2006, Greene et al., 2005, Kocks et al., 2005, Lee et al., 2005, Park et al., 2005, Domazet-Loso and Tautz, 2003, Leulier et al., 2003, Leulier et al., 2003, Yajima et al., 2003, Rutschmann et al., 2002, Tauszig-Delamasure et al., 2002)
        DptA
        (Cha and Kim, 2026, Chen et al., 2026, Dähn et al., 2026, Deng et al., 2026, Fang et al., 2026, Huang and Perrimon, 2026, Mikhailova et al., 2026, Schlomann et al., 2026, Wang et al., 2026, Akyaw et al., 2025, Bayar et al., 2025, Golubev et al., 2025, Kang et al., 2025, Lee et al., 2025, Qush et al., 2025, Rommelaere et al., 2025, Sheng et al., 2025, Soteriou et al., 2025, Webster and Polak, 2025, Yao et al., 2025, Zheng et al., 2025, Arias-Rojas et al., 2024, Beghelli et al., 2024, Guo et al., 2024, Hachfi et al., 2024, Isaacson et al., 2024, Krejčová et al., 2024, Liang et al., 2024, Meyer et al., 2024, Nicolson et al., 2024, Nigg et al., 2024, Prakash et al., 2024, Salminen et al., 2024, Vesala et al., 2024, Westlake et al., 2024, Yao et al., 2024, Arias-Rojas et al., 2023, Bossen et al., 2023, Chen et al., 2023, Elguero et al., 2023, Hsieh and Chiang, 2023, Huang et al., 2023, Kuyateh and Obbard, 2023, Lee et al., 2023, Muita and Baxter, 2023, Stączek et al., 2023, Touré et al., 2023, Deshpande et al., 2022, Eickelberg et al., 2022, Hong et al., 2022, Kim et al., 2022, Li et al., 2022, Liu et al., 2022, Shit et al., 2022, Takeuchi et al., 2022, Vaibhvi et al., 2022, Waring et al., 2022, Wu and Yan, 2022, Wu et al., 2022, Hall et al., 2021, Yamashita et al., 2021, Zhou et al., 2021, Cai et al., 2020, Kwon et al., 2020, Lim et al., 2020, Seong et al., 2020, Sun et al., 2020, Swanson et al., 2020, Swanson et al., 2020, Asri et al., 2019, Baenas and Wagner, 2019, Chambers et al., 2019, Chen et al., 2019, Houtz et al., 2019, Moskalev et al., 2019, Si et al., 2019, Štětina et al., 2019, Troha and Buchon, 2019, Wen et al., 2019, Gene Disruption Project members, 2018-, Hemphill et al., 2018, Kamareddine et al., 2018, Li et al., 2018, Mlih et al., 2018, Schretter et al., 2018, Early et al., 2017, Huang et al., 2017, Kiss et al., 2016, Gendrin et al., 2013, Galac and Lazzaro, 2011, Sackton et al., 2010, Feng et al., 2009, Hill-Burns and Clark, 2009, Hedengren-Olcott et al., 2004, Lazzaro et al., 2004, Hedengren et al., 2000)
        Name Synonyms
        Diptericin
        (Karlsberger et al., 2026, Knop et al., 2025, Toubarro et al., 2025, Yuan et al., 2025, Darby et al., 2024, Feng et al., 2024, Nainu et al., 2024, Nguyen et al., 2024, Tsap et al., 2024, Zhu et al., 2024, Arch et al., 2023, Chen et al., 2023, Parks et al., 2023, Chen et al., 2022, Delventhal et al., 2022, Eleftherianos and Tafesh-Edwards, 2022, Pratomo et al., 2022, Singh and Tapadia, 2022, Yu et al., 2022, Eleftherianos and Heryanto, 2021, Harnish et al., 2021, Marra et al., 2021, Ozakman and Eleftherianos, 2021, Rydbom et al., 2021, Deng et al., 2020, Hanson and Lemaitre, 2020, Iwashita et al., 2020, Ozakman and Eleftherianos, 2020, Younes et al., 2020, Aalto et al., 2019, Ji et al., 2019, Sanchez Bosch et al., 2019, Westfall et al., 2019, Yadav and Eleftherianos, 2019, Akagi et al., 2018, Garschall and Flatt, 2018, Hleihel et al., 2018, Hori et al., 2018, Sherri et al., 2018, Su et al., 2018, Yuan et al., 2018, Capo et al., 2017, Duneau et al., 2017, Jones et al., 2017, Tavignot et al., 2017, Akbar et al., 2016, Allen et al., 2016, Helenius et al., 2016, Ji et al., 2016, Neyen et al., 2016, Sekihara et al., 2016, Xiong et al., 2016, Arefin et al., 2015, Bandarra et al., 2015, Castillo et al., 2015, Pragya et al., 2015, Shirinian et al., 2015, Terhzaz et al., 2015, Wu et al., 2015, Yamamoto-Hino et al., 2015, Binggeli et al., 2014, Chakrabarti et al., 2014, Goto et al., 2014, Haller et al., 2014, Ji et al., 2014, Tan et al., 2014, Varma et al., 2014, Zhou et al., 2014, Aparicio et al., 2013, Clark et al., 2013, Dantoft et al., 2013, Ferrandon, 2013, Furihata et al., 2013, Gendrin et al., 2013, Oh et al., 2013, Quintin et al., 2013, Vandersmissen et al., 2013, Yagi et al., 2013, An et al., 2012, Bier and Guichard, 2012, Bosco-Drayon et al., 2012, Choi and Hyun, 2012, Keebaugh and Schlenke, 2012, Longworth et al., 2012, Marek and Kagan, 2012, Neyen et al., 2012, Petersen et al., 2012, Tsuzuki et al., 2012, Wu et al., 2012, Akbar et al., 2011, Akhouayri et al., 2011, Chtarbanova and Imler, 2011, Clark et al., 2011, Esfahani and Engström, 2011, Fellous and Lazzaro, 2011, Kuraishi et al., 2011, Limmer et al., 2011, Mulcahy et al., 2011, Opota et al., 2011, Ragab et al., 2011, Schmidt et al., 2011, Wang et al., 2011, Zaidman-Rémy et al., 2011, Zhao et al., 2011, Aymeric et al., 2010, Becker et al., 2010, Buchon et al., 2010, Goto et al., 2010, Haghayeghi et al., 2010, Kurata, 2010, Lemos et al., 2010, Moule et al., 2010, Paquette et al., 2010, Radyuk et al., 2010, Tanji et al., 2010, Yagi et al., 2010, Zhao et al., 2010, Buchon et al., 2009, Buchon et al., 2009, Carpenter et al., 2009, Charroux and Royet, 2009, Choi et al., 2009, Costa et al., 2009, Diangelo et al., 2009, Ertürk-Hasdemir et al., 2009, Gendrin et al., 2009, Wei et al., 2009, Wiklund et al., 2009, Aggarwal et al., 2008, Bergeret et al., 2008, Deddouche et al., 2008, Flatt et al., 2008, Goto et al., 2008, Jin et al., 2008, Lhocine et al., 2008, Maillet et al., 2008, Reed et al., 2008, Ryu et al., 2008, Scherfer et al., 2008, Schmidt et al., 2008, Sekiya et al., 2008, Tang et al., 2008, Vonkavaara et al., 2008, Dijkers and O'Farrell, 2007, Harari-Steinberg et al., 2007, Helenius et al., 2007, Lesch et al., 2007, Pal et al., 2007, Tanji et al., 2007, Taylor and Kimbrell, 2007, Valanne et al., 2007, Waterhouse et al., 2007, Wu et al., 2007, Kambris et al., 2006, Leulier et al., 2006, Libert et al., 2006, Liehl et al., 2006, Matova and Anderson, 2006, Mulinari et al., 2006, Senger et al., 2006, Zraly et al., 2006, Johansson et al., 2005, Sano et al., 2005, Shin et al., 2005, Zhou et al., 2005, Bassett et al., 2003, Leulier et al., 2003, Yajima et al., 2003, Chen et al., 2002, Ligoxygakis et al., 2002, Naitza et al., 2002, Roxstrom-Lindquist et al., 2002, Rutschmann et al., 2002, Tauszig-Delamasure et al., 2002, Kimbrell and Beutler, 2001, Lindmark et al., 2001, Luo et al., 2001, Rutschmann et al., 2000, Reichhart, 1992.2.19)
        Diptericin (A)
        Diptericin precursor
        diptericin
        (Azizpor et al., 2025, Kumar et al., 2025, Shiratsuchi et al., 2024, Aalto et al., 2023, Lee et al., 2023, Benoit et al., 2022, Kong et al., 2021, Mishra et al., 2021, Wagner et al., 2021, Zhu et al., 2021, Badinloo et al., 2018, Wei et al., 2018, Lee et al., 2017, Shaw et al., 2017, Park et al., 2016, Regan et al., 2016, Shiratsuchi et al., 2016, Bandarra et al., 2015, Kutch and Fedorka, 2015, Shirinian et al., 2015, Verma and Tapadia, 2015, Hang et al., 2014, Verma and Tapadia, 2014, Bonnay et al., 2013, Fontenele et al., 2013, Gonzalez et al., 2013, Kemp et al., 2013, Nelson et al., 2013, Bier and Guichard, 2012, Bitra et al., 2012, Chambers et al., 2012, Hamilos et al., 2012, Igboin et al., 2012, Jones et al., 2012, Kounatidis and Ligoxygakis, 2012, Lemaitre et al., 2012, Meinander et al., 2012, Overend et al., 2012, Rera et al., 2012, Verma and Tapadia, 2012, Wang et al., 2012, Douglas et al., 2011, Igboin et al., 2011, Anbutsu and Fukatsu, 2010, Garbuzov and Tatar, 2010, Mabery and Schneider, 2010, Radyuk et al., 2010, Avadhanula et al., 2009, Berkey et al., 2009, Brown et al., 2009, Guntermann et al., 2009, Hashimoto et al., 2009, Luce-Fedrow et al., 2009, Merkle et al., 2009, Okado et al., 2009, Saleh et al., 2009, Shia et al., 2009, Stergiopoulos et al., 2009, Wagner et al., 2009, Zhang and Palli, 2009, Jones et al., 2008, Kapelnikov et al., 2008, Lee and Edery, 2008, Malagoli et al., 2008, Ratnaparkhi and Courey, 2008, Ratnaparkhi et al., 2008, Sibley et al., 2008, Silverman et al., 2008, Avet-Rochex et al., 2007, Brennan et al., 2007, Copley et al., 2007, Domanitskaya et al., 2007, Ferrarese et al., 2007, Hallem et al., 2007, Huh et al., 2007, Ren et al., 2007, Bischoff et al., 2006, Delaney et al., 2006, Johansson et al., 2006, Kaneko et al., 2006, Kim et al., 2006, Kim et al., 2006, Avet-Rochex et al., 2005, Delaney et al., 2005, Tsuda et al., 2005, Zerofsky et al., 2005, Leclerc and Reichhart, 2004, Agaisse et al., 2003, Cha et al., 2003, Janssens and Beyaert, 2003, Leulier et al., 2003, Fauvarque et al., 2002, Ligoxtgakis, 2002, Mukae et al., 2002, Wicker et al., 1990)
        Secondary FlyBase IDs
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          External Crossreferences and Linkouts ( 62 )
          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 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
          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.
          BDGP expression data - Patterns of gene expression in Drosophila embryogenesis
          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
          InterPro - A database of protein families, domains and functional sites
          KEGG Genes - Molecular building blocks of life in the genomic space.
          MARRVEL_MODEL - MARRVEL (model organism gene)
          Linkouts
          Drosophila Genomics Resource Center - Drosophila Genomics Resource Center (DGRC) cDNA clones
          DroID - A comprehensive database of gene and protein interactions.
          DRSC - Results frm RNAi screens
          Eukaryotic Promoter Database - A collection of databases of experimentally validated promoters for selected model organisms.
          FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
          FlyCyc Genes - Genes from a BioCyc PGDB for Dmel
          Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
          KEGG Pathways - A collection of manually drawn pathway maps representing knowledge of molecular interaction, reaction and relation networks.
          References (824)