FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Gene: Dmel\cyc
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General Information
Symbol
Dmel\cyc
Species
D. melanogaster
Name
cycle
Annotation Symbol
CG8727
Feature Type
FlyBase ID
FBgn0023094
Gene Model Status
Stock Availability
Gene Summary
cycle (cyc) is a circadian clock gene. It encodes a transcription factor of the BHLH-PAS family and activates transcription of key clock genes as well as downstream clock-regulated genes. [Date last reviewed: 2018-09-20] (FlyBase Gene Snapshot)
Also Known As

dbmal1, BMAL1, dCYC

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
3-46
RefSeq locus
NT_037436 REGION:19813770..19815938
Sequence
Genomic Maps
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
Gene Ontology (GO) Annotations (24 terms)
Molecular Function (7 terms)
Terms Based on Experimental Evidence (3 terms)
CV Term
Evidence
References
enables DNA binding
inferred from direct assay
inferred from physical interaction with UniProtKB:O61735
Terms Based on Predictions or Assertions (4 terms)
CV Term
Evidence
References
Biological Process (13 terms)
Terms Based on Experimental Evidence (4 terms)
CV Term
Evidence
References
inferred from mutant phenotype
inferred from mutant phenotype
inferred from direct assay
Terms Based on Predictions or Assertions (10 terms)
CV Term
Evidence
References
Cellular Component (4 terms)
Terms Based on Experimental Evidence (0 terms)
Terms Based on Predictions or Assertions (4 terms)
CV Term
Evidence
References
inferred from biological aspect of ancestor with PANTHER:PTN000548496
located_in cytoplasm
inferred from electronic annotation with InterPro:IPR001067
is_active_in nucleus
inferred from biological aspect of ancestor with PANTHER:PTN000548496
located_in nucleus
inferred from electronic annotation with InterPro:IPR001067
Protein Family (UniProt)
-
Summaries
Gene Snapshot
cycle (cyc) is a circadian clock gene. It encodes a transcription factor of the BHLH-PAS family and activates transcription of key clock genes as well as downstream clock-regulated genes. [Date last reviewed: 2018-09-20]
Gene Group (FlyBase)
BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS -
Basic helix-loop-helix (bHLH) transcription factors are sequence-specific DNA-binding proteins that regulate transcription. They are characterized by a 60 amino acid region comprising a basic DNA binding domain followed by a HLH motif formed from two amphipathic α-helices connected by a loop. bHLH transcription factors form homo- and hetero-dimeric complexes, which bind to a E box consensus sequence. (Adapted from PMID:15186484).
Protein Function (UniProtKB)
Putative transcription factor involved in the generation of biological rhythms. Activates cycling transcription of Period (PER) and Timeless (TIM) by binding to the E-box (5'-CACGTG-3') present in their promoters.
(UniProt, O61734)
Summary (Interactive Fly)

transcription factor - bHLH, pas domain - photoperiod response - Clock-Cycle heterodimer binds canonical E-box sequences to activate the transcription of direct targets clockwork orange, period, timeless, vrille and par domain protein 1

Gene Model and Products
Number of Transcripts
1
Number of Unique Polypeptides
1

Please see the JBrowse view of Dmel\cyc 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 O61734)

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

Gene model reviewed during 5.45

Gene model reviewed during 5.43

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

Gene model reviewed during 5.46

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0074924
1625
413
Additional Transcript Data and Comments
Reported size (kB)

1.7 (northern blot)

Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
UniProt
RefSeq ID
GenBank
FBpp0074693
47.6
413
7.71
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)
Comments
External Data
Subunit Structure (UniProtKB)

Efficient DNA binding requires dimerization with another bHLH protein. Forms a heterodimer with Clock in order to activate PER and TIM transcription.

(UniProt, O61734)
Crossreferences
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\cyc 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).

-0.52

Transcript Expression
in situ
Stage
Tissue/Position (including subcellular localization)
Reference
organism

Comment: maternally deposited

northern blot
Stage
Tissue/Position (including subcellular localization)
Reference
RT-PCR
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data

The amount of cyc is reduced slightly in old flies compared to young flies, with the difference being slightly more pronounced in heads than in bodies.

cyc transcripts are detected in adult head RNA. They do not exhibit any temporal cycling.

Marker for
 
Subcellular Localization
CV Term
Polypeptide Expression
Additional Descriptive Data
Marker for
 
Subcellular Localization
CV Term
Evidence
References
Expression Deduced from Reporters
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\cyc 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
Flygut - An atlas of the Drosophila adult midgut
Images
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 7 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 24 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of cyc
Transgenic constructs containing regulatory region of cyc
Aberrations (Deficiencies and Duplications) ( 1 )
Inferred from experimentation ( 1 )
Inferred from location ( 2 )
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) (38)
12 of 14
Yes
Yes
1  
11 of 14
No
Yes
4 of 14
No
No
4 of 14
No
No
2 of 14
No
No
1  
2 of 14
No
No
2  
2 of 14
No
No
1  
2 of 14
No
No
2 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
4  
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 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  
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
1  
1 of 14
No
No
3  
1 of 14
No
No
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Rattus norvegicus (Norway rat) (31)
12 of 14
Yes
Yes
9 of 14
No
Yes
4 of 14
No
No
4 of 14
No
No
2 of 14
No
No
2 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) (32)
12 of 14
Yes
Yes
11 of 14
No
Yes
4 of 14
No
No
3 of 14
No
No
2 of 14
No
No
2 of 14
No
No
2 of 14
No
No
2 of 14
No
No
2 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
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  
1 of 14
No
No
1 of 14
No
No
Xenopus tropicalis (Western clawed frog) (31)
8 of 13
Yes
Yes
6 of 13
No
Yes
3 of 13
No
No
2 of 13
No
No
2 of 13
No
No
2 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
Yes
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
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
Yes
1 of 13
No
No
Danio rerio (Zebrafish) (51)
11 of 14
Yes
Yes
10 of 14
No
Yes
10 of 14
No
Yes
3 of 14
No
No
3 of 14
No
No
2 of 14
No
No
2 of 14
No
No
2 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
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) (5)
4 of 14
Yes
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) (19)
12 of 12
Yes
Yes
Arabidopsis thaliana (thale-cress) (7)
1 of 13
Yes
Yes
1 of 13
Yes
Yes
1 of 13
Yes
Yes
1 of 13
Yes
Yes
1 of 13
Yes
Yes
1 of 13
Yes
No
1 of 13
Yes
No
Saccharomyces cerevisiae (Brewer's yeast) (1)
1 of 13
Yes
No
Schizosaccharomyces pombe (Fission yeast) (0)
Escherichia coli (enterobacterium) (0)
Other Organism Orthologs (via OrthoDB)
Data provided directly from OrthoDB:cyc. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Drosophila melanogaster (Fruit fly) (19)
6 of 13
3 of 13
3 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
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 ( 0 )
Allele
Disease
Interaction
References
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
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)
Efficient DNA binding requires dimerization with another bHLH protein. Forms a heterodimer with Clock in order to activate PER and TIM transcription.
(UniProt, O61734 )
Linkouts
BioGRID - A database of protein and genetic interactions.
DroID - A comprehensive database of gene and protein interactions.
MIST (protein-protein) - An integrated Molecular Interaction Database
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)
3L
Recombination map
3-46
Cytogenetic map
Sequence location
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
76C6-76C6
Limits computationally determined from genome sequence between P{lacW}l(3)L3809L3809 and P{lacW}l(3)L1243L1243&P{lacW}Mi-2j3D4
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
76C-76C
(determined by in situ hybridisation)
Experimentally Determined Recombination Data
Left of (cM)
Right of (cM)
Notes
Stocks and Reagents
Stocks (20)
Genomic Clones (8)
 

Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete

cDNA Clones (18)
 

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
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

    DNA-protein interactions: genome-wide binding profile (ChIP-chip) assayed for cyc protein in adult heads; see GEO_GSE32613 (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE32613).

    Clk and cyc proteins interact in the cytoplasm of S2R+ cells and heterodimerisation promotes nuclear import as well as phosphorylation of cytoplasmic Clk protein.

    cry functions as a repressor of Clk/cyc-activated transcription.

    dco-mediated hyperphosphorylation of Clk does not require cyc or the DNA-binding domain of Clk.

    Clk and cyc, along with other circadian genes per and dco (but not tim) have roles in regulating cocaine sensitization and may function as regulators of Tdc.

    Sensitization to repeated cocaine exposures, a phenomenon also seen in humans and animal models and associated with enhanced drug craving, is eliminated in flies mutant for per, dco, Clk, and cyc but not tim.

    Clk mRNA cycling is regulated by per-tim-mediated release of Clk- and cyc-dependent repression.

    Daily cycles in the association of per and tim proteins with the Clk-cyc complex may contribute to rhythmic expression of per and tim.

    The tim-induced per mRNA level increase does not require cyc.

    Mutation of the cyc gene produces flies that are behaviourally arrhythmic and have little per or tim transcription.

    Arrhythmic mutant. per and tim transcription levels are low and constant in cyc mutants.

    Relationship to Other Genes
    Source for database merge of

    Source for merge of: cyc Mop3

    Additional comments

    Source for merge of cyc Mop3 was sequence comparison ( date:000202 ).

    Nomenclature History
    Source for database identify of
    Nomenclature comments
    Etymology
    Synonyms and Secondary IDs (22)
    Reported As
    Symbol Synonym
    Mop3
    cyc
    (Liao et al., 2025, Wang et al., 2025, Liu et al., 2024, Peng et al., 2024, Peterson and Ahmad, 2024, Shirakawa et al., 2024, Anna et al., 2023, Gao et al., 2023, Khatib et al., 2023, Liu et al., 2023, Rodrigues et al., 2023, Tuo et al., 2023, Jarabo et al., 2022, Philyaw et al., 2022, Poe et al., 2022, Sebastian et al., 2022, Sheardown et al., 2022, Vaughen et al., 2022, Yildirim et al., 2022, Zhao et al., 2022, Ahmad et al., 2021, Cavieres-Lepe and Ewer, 2021, Du et al., 2021, Gunawardhana et al., 2021, Ibaraki et al., 2021, Khyati et al., 2021, Solovev et al., 2021, Zhang et al., 2021, Beer and Helfrich-Förster, 2020, Brody, 2020, Damulewicz et al., 2020, De Nobrega and Lyons, 2020, Funato, 2020, Helfrich-Förster et al., 2020, Hill et al., 2020, Lathen et al., 2020, Mahesh et al., 2020, Ulgherait et al., 2020, Wang et al., 2020, Boomgarden et al., 2019, Bulthuis et al., 2019, Cho et al., 2019, Harbison et al., 2019, Hegazi et al., 2019, Hsieh et al., 2019, Martin Anduaga et al., 2019, Meltzer, 2019-, Meltzer et al., 2019, Mendoza and Vanotti, 2019, Shokri et al., 2019, Sinigaglia et al., 2019, Solovev et al., 2019, Stone et al., 2019, Zhao et al., 2019, Bischof et al., 2018, Chatterjee et al., 2018, Doupé et al., 2018, Filošević et al., 2018, Gene Disruption Project members, 2018-, Nazario-Toole et al., 2018, Noreen et al., 2018, Parasram et al., 2018, Zhang et al., 2018, Gunawardhana and Hardin, 2017, Lee et al., 2017, Liu et al., 2017, Park et al., 2017, Selcho et al., 2017, Sharp et al., 2017, Transgenic RNAi Project members, 2017-, Vaccaro et al., 2017, Donelson and Sanyal, 2015, Giebultowicz and Long, 2015, Gill et al., 2015, Grotewiel and Bettinger, 2015, Lerner et al., 2015, Liu et al., 2015, Pasco et al., 2015, Schertel et al., 2015, Tataroglu and Emery, 2015, Thimgan et al., 2015, Tomita et al., 2015, Zwarts et al., 2015, Glossop et al., 2014, Liu et al., 2014, Victorsen and White, 2014.4.15, Joiner et al., 2013, Krupp et al., 2013, Lee et al., 2013, Lim and Allada, 2013, Mehta and Cheng, 2013, Pandey et al., 2013, Pohl et al., 2013, Rakshit et al., 2013, Sivachenko et al., 2013, Bywalez et al., 2012, Chen et al., 2012, Japanese National Institute of Genetics, 2012.5.21, Kaun et al., 2012, Luo et al., 2012, Rakshit et al., 2012, Ruben et al., 2012, Abruzzi et al., 2011, Diangelo et al., 2011, Goda et al., 2011, Ito et al., 2011, Itoh et al., 2011, Lone and Sharma, 2011, Beaver et al., 2010, Blanchard et al., 2010, Chatterjee et al., 2010, Cooper et al., 2010, Fujii and Amrein, 2010, Gegear et al., 2010, Keene et al., 2010, Kula-Eversole et al., 2010, Li et al., 2010, Menet et al., 2010, Nagoshi et al., 2010, Thimgan et al., 2010, Xie et al., 2010, Bahn et al., 2009, Currie et al., 2009, Dworkin et al., 2009, Fathallah-Shaykh et al., 2009, Gummadova et al., 2009, Hung et al., 2009, Kempinger et al., 2009, Kilman and Allada, 2009, Maurer et al., 2009, Sehadova et al., 2009, Benito et al., 2008, Fujii et al., 2008, Houl et al., 2008, Ito et al., 2008, Kadener et al., 2008, Krishnan et al., 2008, Lee and Edery, 2008, Miura et al., 2008, Ogawa et al., 2008, Ratan et al., 2008, Tanoue et al., 2008, Taylor and Hardin, 2008, T et al., 2008, Xu et al., 2008, Yang et al., 2008, Fujii et al., 2007, Hung et al., 2007, Kurata et al., 2007, Lim et al., 2007, Vosshall, 2007, Williams et al., 2007, Yoshii et al., 2007, Chen et al., 2006, Ganguly-Fitzgerald et al., 2006, Ni et al., 2006, Rosbash, 2006.8.10, Seugnet et al., 2006, Van Gelder, 2006, Yuan et al., 2006, Cyran et al., 2005, Mazzoni et al., 2005, Yuan et al., 2005, Yuan et al., 2005, Beaver et al., 2003, Hendricks et al., 2003, Yoshii et al., 2002)
    Secondary FlyBase IDs
    • FBgn0024953
    • FBgn0025108
    Datasets (0)
    Study focus (0)
    Experimental Role
    Project
    Project Type
    Title
    Study result (0)
    Result
    Result Type
    Title
    External Crossreferences and Linkouts ( 56 )
    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
    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
    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
    BioGRID - A database of protein and genetic interactions.
    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
    Flygut - An atlas of the Drosophila adult midgut
    iBeetle-Base - RNAi phenotypes in the red flour beetle (Tribolium castaneum)
    Interactive Fly - A cyberspace guide to Drosophila development and metazoan evolution
    KEGG Pathways - A collection of manually drawn pathway maps representing knowledge of molecular interaction, reaction and relation networks.
    MIST (protein-protein) - An integrated Molecular Interaction Database
    References (458)