FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Gene: Dmel\dpn
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General Information
Symbol
Dmel\dpn
Species
D. melanogaster
Name
deadpan
Annotation Symbol
CG8704
Feature Type
FlyBase ID
FBgn0010109
Gene Model Status
Stock Availability
Gene Summary
Transcriptional repressor of genes that require a bHLH protein for their transcription (PubMed:1427077, PubMed:24618901, PubMed:28899667). In the larval brain, required to maintain the self-renewal and identity of type II neuroblasts by regulating the expression of the transcriptional repressor erm together with other self-renewal transcriptional repressors such as klu and E(spl)mgamma-HLH (PubMed:21262215, PubMed:22357926, PubMed:23056424, PubMed:24618901, PubMed:28899667). As part of its role in neuroblasts development, has been shown to be a direct target of the Notch signaling pathway, however might work also independently of N/Notch (PubMed:21262215, PubMed:22357926, PubMed:23056424). In the developing larval and pupal brain, required for mushroom body differentiation (PubMed:22357926). Involved in sex determination and SXL transcription repression when in complex with the corepressor protein Groucho (PubMed:7651341, PubMed:8001118). (UniProt, Q26263)
Contribute a Gene Snapshot for this gene.
Also Known As

44C

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
2-58
RefSeq locus
NT_033778 REGION:8228971..8232330
Sequence
Genomic Maps
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
Gene Ontology (GO) Annotations (25 terms)
Molecular Function (9 terms)
Terms Based on Experimental Evidence (6 terms)
CV Term
Evidence
References
Terms Based on Predictions or Assertions (4 terms)
CV Term
Evidence
References
Biological Process (14 terms)
Terms Based on Experimental Evidence (11 terms)
CV Term
Evidence
References
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from direct assay
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from genetic interaction with UniProtKB:P29617
inferred from mutant phenotype
inferred from mutant phenotype
inferred from genetic interaction with UniProtKB:P51023
inferred from genetic interaction with UniProtKB:Q8MQJ9
inferred from genetic interaction with UniProtKB:Q9VQ56
inferred from genetic interaction with UniProtKB:M9PF84
inferred from genetic interaction with UniProtKB:Q94517
inferred from mutant phenotype
inferred from genetic interaction with FLYBASE:Sxl; FB:FBgn0264270
Terms Based on Predictions or Assertions (4 terms)
CV Term
Evidence
References
Cellular Component (2 terms)
Terms Based on Experimental Evidence (2 terms)
CV Term
Evidence
References
located_in cytosol
inferred from direct assay
located_in nucleus
inferred from direct assay
inferred from mutant phenotype
Terms Based on Predictions or Assertions (1 term)
CV Term
Evidence
References
is_active_in nucleus
inferred from biological aspect of ancestor with PANTHER:PTN004213585
Protein Family (UniProt)
-
Summaries
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)
Transcriptional repressor of genes that require a bHLH protein for their transcription (PubMed:1427077, PubMed:24618901, PubMed:28899667). In the larval brain, required to maintain the self-renewal and identity of type II neuroblasts by regulating the expression of the transcriptional repressor erm together with other self-renewal transcriptional repressors such as klu and E(spl)mgamma-HLH (PubMed:21262215, PubMed:22357926, PubMed:23056424, PubMed:24618901, PubMed:28899667). As part of its role in neuroblasts development, has been shown to be a direct target of the Notch signaling pathway, however might work also independently of N/Notch (PubMed:21262215, PubMed:22357926, PubMed:23056424). In the developing larval and pupal brain, required for mushroom body differentiation (PubMed:22357926). Involved in sex determination and SXL transcription repression when in complex with the corepressor protein Groucho (PubMed:7651341, PubMed:8001118).
(UniProt, Q26263)
Summary (Interactive Fly)

transcription factor - bHLH - hairy/E(spl) class - a pan-neural repressor - regulates the self-renewal and specification of Drosophila larval neural stem cells independently of Notch - required to silence Tramtrack transcription in the R7 photoreceptor precursor in order to determine photoreceptor fate

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

Please see the JBrowse view of Dmel\dpn 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 Q26263)

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 5.49

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0088803
2036
435
Additional Transcript Data and Comments
Reported size (kB)

2.3 (northern blot)

Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
UniProt
RefSeq ID
GenBank
FBpp0087879
46.6
435
7.55
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)

Homodimer (PubMed:22357926, PubMed:7651341). Heterodimer with E(spl)mgamma-HLH and E(spl) (PubMed:22357926). Transcription repression requires formation of a complex with the corepressor protein Groucho (PubMed:8001118). Interacts (via bHLH motif) with sisA (PubMed:7651341). Interacts with da (PubMed:7651341).

(UniProt, Q26263)
Domain

Has a particular type of basic domain (presence of a helix-interrupting proline) that binds to the N-box (CACNAG), rather than the canonical E-box (CANNTG).

The C-terminal WRPW motif is a transcriptional repression domain necessary for the interaction with Groucho, a transcriptional corepressor recruited to specific target DNA by Hairy-related proteins.

(UniProt, Q26263)
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\dpn 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).

-0.34

Transcript Expression
No Assay Recorded
Stage
Tissue/Position (including subcellular localization)
Reference
in situ
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data

dpn is expressed in precellular blastoderm embryos during cycle 13 in a nearly ubiquitous pattern. It is then expressed in a pattern of 8 pair rule stripes. In late germband extension, expression in a rosette pattern is observed. At stage 10 expression is seen in the neuroblasts of each hemisegment along the ventral nerve cord.

No dpn transcripts are detected in dpn1 mutant embryos.

dpn transcripts are first detected in a ubiquitous pattern in embryonic cycle 12. A transient gap-rule pattern in cycle 13 is followed by a pair-rule stripe pattern. dpn stripes overlap with the corresponding h stripes which extend further posteriorly. dpn transcripts are expressed briefly in patches of neurectoderm preceding the first wave of neuroblast segregation and become restricted to the neuroblasts before they delaminate. By 6 1/2-7 hr, all neuroblasts have delaminated and express dpn. In the PNS, dpn is expressed weakly in patches of ectodermal cells followed by strong expression in sensillum precursors. Expression in neural precursors disappears soon after they divide and reappears at later stages of nervous system development of the CNS and PNS as neurons begin to differentiate. dpn is also expressed in neuroblasts of the larval CNS and in precursors of sensory neurons in imaginal discs. Expression is restricted to the primary neural precursor cell. In ventral thoracic discs, expression is also observed in additional non-neuronal cells. dpn expression is absent in neuroblasts in a da mutant background, but is present at normal levels in a reduced number of neuroblasts in a Df(1)sc-B57 background.

Marker for
Subcellular Localization
CV Term
Polypeptide Expression
No Assay Recorded
Stage
Tissue/Position (including subcellular localization)
Reference
immunolocalization
Stage
Tissue/Position (including subcellular localization)
Reference
neuroblast

Comment: Assayed at ~5hr after pupal formation.

neuroblast

Comment: Assayed at ~30hr after pupal formation.

neuroblast

Comment: Assayed at mid-pupal stage.

Additional Descriptive Data

dpn-protein expression can be found in neuroblasts in the distal part of the inner proliferation zone in the larval optic anlage.

dpn protein is localized to type II and secondary neuroblasts, but not to type I neuroblasts.

Approximately 100 neuroblasts in the 96hr 3rd instar larvae central nervous system express dpn. At ~5hr after pupal formation, the number of cells expressing dpn remains the same as in 3rd instar larvae, but cell size and mitotic activity are reduced. Midway through pupal development, only the mushroom body neuroblasts remain. Expression is no longer present 10hr before eclosion (~96hr APF).

dpn is expressed weakly in two to three rows of neural progenitor cells lateral to the l(1)sc-expressing cells in the developing optic lobe and at high levels in the neuroblasts.

No dpn protein is detected in neural precursors in dpn1 mutants.

dpn protein is first detected in a ubiquitous pattern in embryonic cycle 12. A transient gap-rule pattern in cycle 13 is followed by a pair-rule stripe pattern. dpn stripes overlap with the corresponding h stripes which extend further posteriorly. dpn protein is expressed briefly in patches of neurectoderm preceding the first wave of neuroblast segregation and is restricted to the neuroblasts before they delaminate. By 6 1/2-7hr, all neuroblasts have delaminated and express dpn. In the PNS, dpn protein is expressed weakly in patches of ectodermal cells followed by strong expression in sensillum precursors. Expression in neural precursors disappears soon after they divide and reappears at later stages of CNS and PNS development as neurons begin to differentiate. dpn protein is also expressed in neuroblasts of the larval CNS and in precursors of sensory neurons in imaginal discs. Expression is restricted to the primary neural precursor cell. In leg imaginal discs, expression is also observed in additional non-neuronal cells. dpn protein expression is absent in neuroblasts in a da mutant background, but is present at normal levels in a reduced number of neuroblasts in a Df(1)sc-B57 background.

Marker for
Subcellular Localization
CV Term
Evidence
References
located_in cytosol
inferred from direct assay
located_in nucleus
inferred from direct assay
inferred from mutant phenotype
Expression Deduced from Reporters
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\dpn 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
FlyExpress - Embryonic expression images (BDGP data)
  • Stages(s) 4-6
  • Stages(s) 7-8
  • Stages(s) 9-10
  • Stages(s) 11-12
  • Stages(s) 13-16
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 14 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 26 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of dpn
Transgenic constructs containing regulatory region of dpn
Aberrations (Deficiencies and Duplications) ( 8 )
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) (24)
10 of 14
Yes
Yes
10 of 14
Yes
Yes
1  
5 of 14
No
No
3 of 14
No
No
3 of 14
No
No
4  
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
2 of 14
No
No
2 of 14
No
No
1  
2 of 14
No
No
1  
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
6  
1 of 14
No
No
5  
1 of 14
No
No
1 of 14
No
Yes
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Rattus norvegicus (Norway rat) (20)
10 of 14
Yes
Yes
5 of 14
No
No
4 of 14
No
No
3 of 14
No
No
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
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
Yes
Mus musculus (laboratory mouse) (19)
10 of 14
Yes
Yes
4 of 14
No
No
3 of 14
No
No
3 of 14
No
No
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
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
Xenopus tropicalis (Western clawed frog) (24)
9 of 13
Yes
Yes
8 of 13
No
No
4 of 13
No
No
2 of 13
No
Yes
2 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
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
Yes
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
Yes
Danio rerio (Zebrafish) (37)
11 of 14
Yes
Yes
11 of 14
Yes
Yes
5 of 14
No
Yes
4 of 14
No
Yes
3 of 14
No
No
3 of 14
No
No
3 of 14
No
No
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
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
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
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Caenorhabditis elegans (Nematode, roundworm) (2)
5 of 14
Yes
Yes
1 of 14
No
Yes
Anopheles gambiae (African malaria mosquito) (9)
6 of 12
Yes
Yes
Arabidopsis thaliana (thale-cress) (10)
2 of 13
Yes
No
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
No
1 of 13
No
No
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:dpn. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Drosophila melanogaster (Fruit fly) (14)
9 of 13
6 of 13
6 of 13
6 of 13
5 of 13
5 of 13
5 of 13
4 of 13
4 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 ( 3 )
Potential Models Based on Orthology ( 0 )
Human Ortholog
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 4 )
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

Please see the Physical Interaction reports below for full details
protein-protein
Physical Interaction
Assay
References
RNA-protein
Physical Interaction
Assay
References
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)
Homodimer (PubMed:22357926, PubMed:7651341). Heterodimer with E(spl)mgamma-HLH and E(spl) (PubMed:22357926). Transcription repression requires formation of a complex with the corepressor protein Groucho (PubMed:8001118). Interacts (via bHLH motif) with sisA (PubMed:7651341). Interacts with da (PubMed:7651341).
(UniProt, Q26263 )
Linkouts
BioGRID - A database of protein and genetic interactions.
DroID - A comprehensive database of gene and protein interactions.
MIST (genetic) - An integrated Molecular Interaction Database
MIST (protein-protein) - An integrated Molecular Interaction Database
Pathways
Signaling Pathways (FlyBase)
Metabolic Pathways
FlyBase
External Links
External Data
Linkouts
Class of Gene
Genomic Location and Detailed Mapping Data
Chromosome (arm)
2R
Recombination map
2-58
Cytogenetic map
Sequence location
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
44C2-44C2
Limits computationally determined from genome sequence between P{lacW}Rs1k09514&P{lacW}l(2)k03110k03110 and P{lacW}Vps25k08904&P{lacW}ptck02507
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
44C-44C
(determined by in situ hybridisation)
Experimentally Determined Recombination Data
Location
Left of (cM)
Right of (cM)
Notes
Stocks and Reagents
Stocks (23)
Genomic Clones (21)
cDNA Clones (26)
 

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
Cell Line Information
Publicly Available Cell Lines
 
    Other Stable Cell Lines
     
      Other Comments

      Host gene for two maternally inherited stable intronic sequence RNA (sisRNA), referred to as "sisR-4" and the "dpn 5' sisRNA".

      dpn is both necessary and sufficient for maintaining neuroblast self-renewal.

      dpn mutants have defects in larval locomotion.

      dsRNA has been made from templates generated with primers directed against this gene. RNAi of dpn results in increased arborization of ddaD and ddaE neurons, defects in dendrite morphogenesis and reproducible defects in da dendrite development.

      Expression of activated h in early blastoderm embryos causes ectopic Sxl expression and male-specific lethality, implying that the h-related denominator element dpn represses Sxl during sex-determination by directly recognising the early Sxl promoter.

      An extensive genetic screen for dominant suppressors of the female specific lethal sisA mutation identified 10 alleles of dpn but no other loci. By itself dpn cannot account for the masculinizing effect of increased autosomal ploidy, but if other denominator elements exist their contributions must be less than that of dpn. The time course of expression of dpn and Sxl in dpn mutant backgrounds suggests that dpn is required for sex determination only during the later stages of X:A signalling in males, to prevent inappropriate expression of SxlPe in the face of increasing sis gene product levels.

      Ecol\lacZ reporter gene construct demonstrates dpn pan-neural enhancer is composed of CNS and PNS specific subelements.

      dpn gene functions as a dose-dependent negative regulator of Sxl-Pe.

      Transfection assays and in vitro DNA binding experiments indicate that da/sc heterodimers directly activate the Sxl early promoter by binding to both high and low affinity sites. dpn protein represses this activation by specific binding to a unique site within the Sxl early promoter.

      The yeast two hybrid system has been used to demonstrate specific interactions within the sisA, sc, dpn and da group of gene products, and to delimit their interaction domains. The results support and extend the model of the molecular basis of the X/A ratio signal.

      Mutants at dpn show genetic interaction with achaete-scute complex mutants.

      The dpn+ product is involved in mobility of larvae and adults. dpn may act as a denominator element in sex determination, with Sxl mediating male lethality due to imbalance of sc+, dpn+ and maternally provided emc+.

      Relationship to Other Genes
      Source for database merge of

      Source for merge of: dpn anon- EST:fe1B12

      Additional comments
      Nomenclature History
      Source for database identify of
      Nomenclature comments
      Etymology
      Synonyms and Secondary IDs (11)
      Reported As
      Symbol Synonym
      Dpn
      (Liu et al., 2025, Wang et al., 2025, He et al., 2024, Sood et al., 2024, Aughey et al., 2023, Barbaste et al., 2023, Voutyraki et al., 2023, Guan et al., 2022, Hafer et al., 2022, Hildebrandt et al., 2022, Ray and Li, 2022, Soares et al., 2022, Connacher and Goldstrohm, 2021, Li and Hidalgo, 2021, Rajan et al., 2021, Hailstone et al., 2020, Hakes and Brand, 2020, Nakamura et al., 2020, Tindell et al., 2020, Bivik Stadler et al., 2019, Piggott et al., 2019, Ramon-Cañellas et al., 2019, Zhang et al., 2019, Abed et al., 2018, Hakes et al., 2018, Schwartz and Rhiner, 2018, Shaikh and Tejedor, 2018, An et al., 2017, Caygill and Brand, 2017, Mavromatakis and Tomlinson, 2017, Altenhein et al., 2016, Mukherjee et al., 2016, Shaikh et al., 2016, Apitz and Salecker, 2015, Arya et al., 2015, Fernández-Hernández and Rhiner, 2015, Jia et al., 2015, To et al., 2015, Eroglu et al., 2014, Kuang et al., 2014, Lai and Doe, 2014, Carney et al., 2013, Chai et al., 2013, Chen et al., 2013, Goh et al., 2013, Kux et al., 2013, Lee et al., 2013, Li et al., 2013, Pérez-Gómez et al., 2013, Suzuki et al., 2013, Wang et al., 2013, Zhou and Luo, 2013, Andersen et al., 2012, Callan et al., 2012, Haenfler et al., 2012, Hirono et al., 2012, Kelsom and Lu, 2012, Moraru et al., 2012, Song and Lu, 2012, Ulvklo et al., 2012, Weng and Cohen, 2012, Weng et al., 2012, Xiao et al., 2012, Barry et al., 2011, Benito-Sipos et al., 2011, Hwang and Rulifson, 2011, Kawamori et al., 2011, Morante et al., 2011, Neumüller et al., 2011, Ouyang et al., 2011, Tan et al., 2011, Viktorin et al., 2011, Wang et al., 2011, Wang et al., 2011, Wang et al., 2011, Weng and Lee, 2011, Zhu et al., 2011, Bayraktar et al., 2010, Berger et al., 2010, Brankatschk and Eaton, 2010, Chang et al., 2010, Karlsson et al., 2010, Monastirioti et al., 2010, Reddy et al., 2010, Siegrist et al., 2010, Sousa-Nunes et al., 2010, Weng et al., 2010, Andrews et al., 2009, Baumgardt et al., 2009, Cabernard and Doe, 2009, Sousa-Nunes et al., 2009, Southall and Brand, 2009, Wang et al., 2009, Boone and Doe, 2008, Bowman et al., 2008, Chabu and Doe, 2008, Yasugi et al., 2008, Egger et al., 2007, Kozhina et al., 2007, Wang et al., 2007, Wang et al., 2007, Lee et al., 2006, Lee et al., 2006, Parrish et al., 2006, Urbach et al., 2006, Wang et al., 2006, Quintero et al., 2005, Winston and Gottesfeld, 2000)
      anon-EST:fe1B12
      dpn
      (Arias and Tomlinson, 2025, Cai and Wang, 2025, El-Danaf et al., 2025, Plygawko et al., 2025, Yun et al., 2025, Ko et al., 2024, Mönch et al., 2024, Cai et al., 2023, Catalani et al., 2022, Simões et al., 2022, Theodorou et al., 2022, Voutyraki et al., 2022, Crocker et al., 2021, Frankenreiter et al., 2021, Martin et al., 2021, Michki et al., 2021, Onur et al., 2021, Surkova et al., 2021, Hassan et al., 2020, Li and Hidalgo, 2020, Li et al., 2020, Magadi et al., 2020, Yoo et al., 2020, Arya et al., 2019, Brunet Avalos et al., 2019, Gahr et al., 2019, Harding and White, 2019, Otsuki and Brand, 2019, Shokri et al., 2019, Tegeder et al., 2019, van den Ameele and Brand, 2019, Zhou et al., 2019, Aughey et al., 2018, Bischof et al., 2018, Komori et al., 2018, Li et al., 2018, Loewen et al., 2018, Mora et al., 2018, Paul et al., 2018, Pek, 2018, Reichardt et al., 2018, Vaufrey et al., 2018, Chan et al., 2017, Janssens et al., 2017, Karaiskos et al., 2017, Li et al., 2017, Tay and Pek, 2017, Transgenic RNAi Project members, 2017-, Wu et al., 2017, Mavromatakis and Tomlinson, 2016, Morrissy et al., 2016, Urbach et al., 2016, Zacharioudaki et al., 2016, Gene Disruption Project members, 2015-, Huang et al., 2015, Liu et al., 2015, Loedige et al., 2015, Schertel et al., 2015, To et al., 2015, Awasaki et al., 2014, Awasaki et al., 2014, Ciglar et al., 2014, Córdoba and Estella, 2014, Eroglu et al., 2014, Gokcezade et al., 2014, Janssens et al., 2014, Komori et al., 2014, Southall et al., 2014, Aleksic et al., 2013, Babaoğlan et al., 2013, Chai et al., 2013, Berger et al., 2012, Carney et al., 2012, Hadar et al., 2012, Japanese National Institute of Genetics, 2012.5.21, Kunz et al., 2012, San Juan et al., 2012, Zacharioudaki et al., 2012, Zhu et al., 2012, Cave et al., 2011, Colonques et al., 2011, Hasegawa et al., 2011, Kappes et al., 2011, Kuzin et al., 2011, Michaut et al., 2011, Nien et al., 2011, San-Juán and Baonza, 2011, Duncan and Dearden, 2010, Egger et al., 2010, Gladstein et al., 2010, Suissa et al., 2010, Yasugi et al., 2010, Kang et al., 2009, Krejcí et al., 2009, Liang et al., 2008, Lu et al., 2008, Bartolome and Charlesworth, 2006, Molnar et al., 2006, Macdonald and Long, 2005, Reeves and Posakony, 2005, Schlatter and Maier, 2005, Grad et al., 2004, Wallace et al., 2000)
      Name Synonyms
      anon-fast-evolving-1B12
      Secondary FlyBase IDs
      • FBgn0025271
      Datasets (0)
      Study focus (0)
      Experimental Role
      Project
      Project Type
      Title
      Study result (0)
      Result
      Result Type
      Title
      External Crossreferences and Linkouts ( 61 )
      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
      KEGG Genes - Molecular building blocks of life in the genomic space.
      MARRVEL_MODEL - MARRVEL (model organism gene)
      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
      MIST (genetic) - An integrated Molecular Interaction Database
      MIST (protein-protein) - An integrated Molecular Interaction Database
      References (434)