FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Gene: Dmel\nej
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General Information
Symbol
Dmel\nej
Species
D. melanogaster
Name
nejire
Annotation Symbol
CG15319
Feature Type
FlyBase ID
FBgn0261617
Gene Model Status
Stock Availability
Gene Summary
nejire (nej) encodes the transcriptional co-activator CBP. It acetylates several nuclear proteins, including the histone encoded by His3 on K18, K27, and H4 on K8. By regulating gene expression, the product of nej has roles in cell proliferation, cell signaling and differentiation, and in developmental patterning. [Date last reviewed: 2019-03-14] (FlyBase Gene Snapshot)
Also Known As

CBP, dCBP, CREB-binding protein, CREB binding protein, CBP/p300

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
1-29
RefSeq locus
NC_004354 REGION:9665442..9687066
Sequence
Genomic Maps
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
Gene Ontology (GO) Annotations (39 terms)
Molecular Function (12 terms)
Terms Based on Experimental Evidence (8 terms)
CV Term
Evidence
References
inferred from physical interaction with FLYBASE:mod; FB:FBgn0002780
inferred from physical interaction with FLYBASE:Clk; FB:FBgn0023076
inferred from genetic interaction with FLYBASE:ci; FB:FBgn0004859
inferred from direct assay
inferred from genetic interaction with FLYBASE:per; FB:FBgn0003068
Terms Based on Predictions or Assertions (6 terms)
CV Term
Evidence
References
Biological Process (20 terms)
Terms Based on Experimental Evidence (18 terms)
CV Term
Evidence
References
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
involved_in locomotor rhythm
inferred from mutant phenotype
inferred from mutant phenotype
inferred from genetic interaction with FLYBASE:ci; FB:FBgn0004859
inferred from mutant phenotype
inferred from mutant phenotype
inferred from genetic interaction with FLYBASE:ci; FB:FBgn0004859
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from genetic interaction with FLYBASE:Myb; FB:FBgn0002914
involved_in synapse assembly
inferred from mutant phenotype
inferred from mutant phenotype
Terms Based on Predictions or Assertions (3 terms)
CV Term
Evidence
References
Cellular Component (7 terms)
Terms Based on Experimental Evidence (6 terms)
CV Term
Evidence
References
inferred from direct assay
inferred from direct assay
located_in nucleoplasm
inferred from high throughput direct assay
located_in nucleus
inferred from direct assay
inferred from direct assay
inferred from physical interaction with FLYBASE:mod; FB:FBgn0002780
inferred from physical interaction with FLYBASE:ash1; FB:FBgn0005386
Terms Based on Predictions or Assertions (2 terms)
CV Term
Evidence
References
inferred from biological aspect of ancestor with PANTHER:PTN000351795
inferred from biological aspect of ancestor with PANTHER:PTN000351795
Protein Family (UniProt)
-
Catalytic Activity (EC/Rhea)
histone acetyltransferase activity
RHEA 21992:
Summaries
Gene Snapshot
nejire (nej) encodes the transcriptional co-activator CBP. It acetylates several nuclear proteins, including the histone encoded by His3 on K18, K27, and H4 on K8. By regulating gene expression, the product of nej has roles in cell proliferation, cell signaling and differentiation, and in developmental patterning. [Date last reviewed: 2019-03-14]
Gene Group (FlyBase)
TRITHORAX ACETYLATION COMPLEX 1 -
The Trithorax Acetylation Complex 1 (TAC1) possesses histone H3 K4 methyltransferase and histone acetyltransferase activities. (Adapted from FBrf0192625 and FBrf0167942).
HISTONE ACETYLTRANSFERASES -
Histone acetyltransferases catalyze the acetylation of conserved lysine residues on histone proteins by transferring an acetyl group from acetyl CoA to form ε-N-acetyl lysine. (Adapted from PMID:11395403).
Pathway (FlyBase)
NEGATIVE REGULATORS OF WNT-TCF SIGNALING PATHWAY -
Negative regulators of Wnt-TCF (canonical Wnt) signaling down-regulate the pathway, resulting in the attenuation of transcriptional regulation mediated by β-catenin (arm).
POSITIVE REGULATORS OF WNT-TCF SIGNALING PATHWAY -
Positive regulators of Wnt-TCF (canonical Wnt) signaling up-regulate the pathway, resulting in the enhancement of transcriptional regulation mediated by β-catenin (arm).
POSITIVE REGULATORS OF HEDGEHOG SIGNALING PATHWAY -
Positive regulators of hedgehog signaling up-regulate the pathway, resulting in the activation of transcription of hh-responsive genes.
Summary (Interactive Fly)

CBP, a transcriptional co-activator that interacts with a large number of developmentally important transcription factors - acetylates several nuclear proteins, including histone H3 on K18, K27, and H4 on K8. - roles in cell proliferation, cell signaling and differentiation, and in developmental patterning

Gene Model and Products
Number of Transcripts
4
Number of Unique Polypeptides
3

Please see the JBrowse view of Dmel\nej 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 M9MS40)

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

Tissue-specific extension of 3' UTRs observed during later stages (FBrf0218523, FBrf0219848); all variants may not be annotated

Stage-specific extension of 3' UTRs observed during embryogenesis (FBrf0215804); all variants may not be annotated.

Gene model reviewed during 5.43

Gene model reviewed during 5.42

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

Gene model reviewed during 5.46

Annotated transcripts do not represent all supported alternative splices within 5' UTR.

Gene model reviewed during 5.52

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0071402
11733
3276
FBtr0302722
11704
3282
FBtr0302723
15729
3276
FBtr0333521
15400
3266
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
FBpp0071337
340.7
3276
8.86
FBpp0291862
341.4
3282
8.89
FBpp0291863
340.7
3276
8.86
FBpp0305701
339.7
3266
8.86
Polypeptides with Identical Sequences

The group(s) of polypeptides indicated below share identical sequence to each other.

3276 aa isoforms: nej-PB, nej-PD
Additional Polypeptide Data and Comments
Reported size (kDa)

3190 (aa); 332 (kD)

Comments
External Data
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\nej 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).

-0.95

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

Comment: extended 3' UTR isoform

Additional Descriptive Data

Zygotic-specific isoforms of nej with long 3' UTR extensions were observed. The 3' UTR extension isoforms are highly enriched in nervous system tissues.

Marker for
 
Subcellular Localization
CV Term
Polypeptide Expression
immunolocalization
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data
Marker for
 
Subcellular Localization
CV Term
Evidence
References
inferred from direct assay
inferred from direct assay
located_in nucleoplasm
inferred from high throughput direct assay
located_in nucleus
inferred from direct assay
inferred from direct assay
inferred from physical interaction with FLYBASE:mod; FB:FBgn0002780
inferred from physical interaction with FLYBASE:ash1; FB:FBgn0005386
Expression Deduced from Reporters
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\nej 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
Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
Images
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 42 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 34 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of nej
Transgenic constructs containing regulatory region of nej
Aberrations (Deficiencies and Duplications) ( 10 )
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
Sterility
Allele
Other Phenotypes
Allele
Phenotype manifest in
Allele
neuromuscular junction & bouton
neuromuscular junction & bouton, with Scer\GAL4elav.PLu
neuromuscular junction & t-bar
Orthologs
Human Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Homo sapiens (Human) (21)
12 of 14
Yes
Yes
11 of 14
No
Yes
2 of 14
No
No
2 of 14
No
No
1  
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
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  
1 of 14
No
No
1  
1 of 14
No
No
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) (18)
12 of 14
Yes
Yes
3 of 14
No
Yes
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
Mus musculus (laboratory mouse) (22)
12 of 14
Yes
Yes
12 of 14
Yes
Yes
2 of 14
No
Yes
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
Xenopus tropicalis (Western clawed frog) (16)
10 of 13
Yes
Yes
9 of 13
No
Yes
9 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
Yes
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
Danio rerio (Zebrafish) (21)
11 of 14
Yes
Yes
11 of 14
Yes
Yes
10 of 14
No
Yes
10 of 14
No
Yes
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
Caenorhabditis elegans (Nematode, roundworm) (22)
9 of 14
Yes
Yes
4 of 14
No
Yes
3 of 14
No
Yes
3 of 14
No
Yes
3 of 14
No
Yes
2 of 14
No
No
2 of 14
No
Yes
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
Yes
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
Anopheles gambiae (African malaria mosquito) (7)
9 of 12
Yes
Yes
Arabidopsis thaliana (thale-cress) (28)
9 of 13
Yes
Yes
9 of 13
Yes
Yes
8 of 13
No
Yes
8 of 13
No
Yes
6 of 13
No
Yes
2 of 13
No
Yes
2 of 13
No
No
2 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
No
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
Saccharomyces cerevisiae (Brewer's yeast) (9)
2 of 13
Yes
No
2 of 13
Yes
No
1 of 13
No
No
1  
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
Schizosaccharomyces pombe (Fission yeast) (10)
3 of 12
Yes
No
3 of 12
Yes
No
2 of 12
No
Yes
2 of 12
No
No
1 of 12
No
No
1 of 12
No
No
1 of 12
No
No
1 of 12
No
No
1 of 12
No
No
1 of 12
No
No
Escherichia coli (enterobacterium) (0)
Other Organism Orthologs (via OrthoDB)
Data provided directly from OrthoDB:nej. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Drosophila melanogaster (Fruit fly) (12)
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
Human Disease Associations
FlyBase Human Disease Model Reports
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 4 )
Potential Models Based on Orthology ( 3 )
Modifiers Based on Experimental Evidence ( 20 )
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
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
Linkouts
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
Reactome Metabolic Pathways - An open-source, open access, manually curated and peer-reviewed metabolic pathway database.
External Data
Class of Gene
Genomic Location and Detailed Mapping Data
Chromosome (arm)
X
Recombination map
1-29
Cytogenetic map
Sequence location
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
8F7-8F9
Limits computationally determined from genome sequence between P{EP}EP912EP912 and P{EP}nejEP1149&P{EP}nejEP1179
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
8F4-8F8
(determined by in situ hybridisation)
8F4-8F7
(determined by in situ hybridisation)
8F6-8F7
(determined by in situ hybridisation)
8F-9A
(determined by in situ hybridisation)
Experimentally Determined Recombination Data
Location
Left of (cM)
Right of (cM)
Notes
Stocks and Reagents
Stocks (34)
Genomic Clones (23)
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)
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

    Overexpression of nej can repress or activate wg signaling depending on the context.

    RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.

    One of 42 Drosophila genes identified as being most likely to reveal molecular and cellular mechanisms of nervous system development or plasticity relevant to human Mental Retardation disorders.

    nej functions in eye specification. In addition, nej has a role in cell fate determination during eye development, in particular in R3/R4 cell fate choice and also probably in the specification of the R7 photoreceptor.

    nej and Myb work together to promote efficient progression through mitosis.

    Reduction in maternally contributed nej protein levels in embryos leads to reductions in expression of tld, scw, tsg and rho, but not dpp, in early embryogenesis. rho expression is even lost in cells containing signal dependent phosphorylated Mad protein (a marker of BMP signaling).

    nej function is necessary for ci-mediated transactivation of wg during embryogenesis.

    Postsynaptic nej is necessary for normal presynaptic functional development.

    nej functions as a co-activator during dpp signalling. Mad may recruit nej to effect the transcriptional activation of dpp responsive genes during development.

    The nej gene product represses pan to antagonise wg signalling.

    nej is necessary for dl-mediated activation of the twi promoter.

    Isolated from a genomic library using a fragment of the C.elegans CBP gene as a probe, under low stringency conditions.

    nej has been cloned and characterised.

    Using the co-transfection assay with the nej expression plasmid results demonstrate trans-activation by Myb and functional domains of Myb involved in this activity are identified.

    Relationship to Other Genes
    Source for database merge of

    Source for merge of: nej CG15319

    Source for merge of: nej l(1)G0350 l(1)G0112 l(1)G0470 CG15321

    Source for merge of: nej anon-WO03040301.89

    Additional comments

    Annotations CG15321 eliminated in release 5.25 of the genome annotation.

    FlyBase curator comment: "EP1410" overexpression phenotype stated to be due to its effect on nej but orientation of the P{EP} element suggests otherwise.

    FlyBase curator comment: "EP950" overexpression phenotype stated to be due to its effect on nej but orientation of the P{EP} element suggests otherwise. FlyBase curator comment: "EP1410" overexpression phenotype stated to be due to its effect on nej but orientation of the P{EP} element suggests otherwise.

    FlyBase curator comment: "EP950" overexpression phenotype stated to be due to its effect on nej but orientation of the P{EP} element suggests otherwise.

    "l(1)G0464" may affect "nej".

    "l(1)G0350" may affect "CG15321".

    "l(1)G0112" may affect "CG15321".

    "l(1)G0470" may affect "CG15321".

    "l(1)G0350" may affect "CG15321". "l(1)G0286" may affect "CG15321". "l(1)G0137" may affect "CG15321". "l(1)G0112" may affect "CG15321". "l(1)G0270" may affect "CG15321". "l(1)G0470" may affect "CG15321". "l(1)G0236" may affect "CG15321".

    Source for merge of nej anon-WO03040301.89 was sequence comparison ( date:051113 ).

    Nomenclature History
    Source for database identify of
    Nomenclature comments
    Etymology

    'nejire' means 'twist' in Japanese.

    Synonyms and Secondary IDs (37)
    Reported As
    Symbol Synonym
    CBP
    (Marsh et al., 2025, Krasnov et al., 2023, Cho et al., 2022, Nisha and Sarkar, 2022, Yoneda et al., 2022, Furusawa and Emoto, 2021, Mazina et al., 2021, Takakura et al., 2021, Duffraisse et al., 2020, Nakamura et al., 2020, Zraly et al., 2020, Gutierrez-Perez et al., 2019, Haberle et al., 2019, Han et al., 2019, Raj and Sarkar, 2019, Sajwan and Mannervik, 2019, Boija et al., 2017, Chung et al., 2017, Ghezzi et al., 2017, Song et al., 2017, Doiguchi et al., 2016, Flegel et al., 2016, Hirano et al., 2016, Lee et al., 2016, Tie et al., 2016, Baëza et al., 2015, Cutler et al., 2015, Dietz et al., 2015, Ho et al., 2014, Singh et al., 2014, Tie et al., 2014, Zhang et al., 2014, Darbo et al., 2013, Gisselbrecht et al., 2013, Hirano et al., 2013, Zhang et al., 2013, Bodai et al., 2012, Holmqvist et al., 2012, Kellner et al., 2012, Tie et al., 2012, Kirilly et al., 2011, Nègre et al., 2011, Pruteanu-Malinici et al., 2011, Schuettengruber et al., 2011, Boyles et al., 2010, Herz et al., 2010, Mallik and Lakhotia, 2010, Reddy et al., 2010, Das et al., 2009, Smolik, 2009, Tie et al., 2009, Fanti et al., 2008, Parker et al., 2008, Tavantzis and Warrick, 2008, Wang et al., 2008, Fortini, 2007, Hung et al., 2007, Latouche et al., 2007, Li et al., 2007, Lim et al., 2007, Parker et al., 2007, Yin et al., 2007, Parker et al., 2006, Anderson et al., 2005, Eissenberg et al., 2005, Fernandez-Funez et al., 2005, Huen and Chan, 2005, Ma, 2005, Kumar et al., 2004, Lipsick, 2004, Ogden et al., 2004, Sanchez-Elsner and Sauer, 2004, Smith et al., 2004, Yang, 2004, Fernandez-Funez et al., 2003, Petruk et al., 2003, Ingham and McMahon, 2001, Sharpe et al., 2001, Attisano and Wrana, 2000, Chen and Courey, 2000, Glass and Rosenfeld, 2000, Goodman and Smolik, 2000, Kouzarides, 1999, Mannervik et al., 1999, Matise and Joyner, 1999, Murone et al., 1999, Novak and Dedhar, 1999, Anonymous, 1998, Ingham, 1998, Chen, 1997.2.5, Tabin and McMahon, 1997)
    Crbp
    anon-WO0147981.11
    anon-WO03040301.89
    l(1)G0112
    l(1)G0350
    l(1)G0470
    nej
    (Cho and O'Farrell, 2025, Jang et al., 2024, Li et al., 2024, Willnow and Teleman, 2024, Nieken et al., 2023, Titlow et al., 2023, Tu et al., 2023, Di Fede et al., 2022, Ding et al., 2022, Falo-Sanjuan and Bray, 2022, Li and Gavis, 2022, Miao et al., 2022, Velten et al., 2022, Bilder et al., 2021, Gavory et al., 2021, Martin et al., 2021, Raun et al., 2021, Aboukilila et al., 2020, Cho et al., 2020, Graves et al., 2020, Hung et al., 2020, Jeon et al., 2020, Park et al., 2020, Zhao et al., 2020, Nakamura et al., 2019, Sang Cho et al., 2019, Muñoz-Soriano et al., 2018, Rust et al., 2018, Salazar and Yamamoto, 2018, Ghezzi et al., 2017, Janssens et al., 2017, Transgenic RNAi Project members, 2017-, Vallejos Baier et al., 2017, Brewer-Jensen et al., 2016, Malartre, 2016, Maurer et al., 2016, Morimoto et al., 2016, Moulton and Letsou, 2016, Schwartz et al., 2016, Yu et al., 2016, Jia et al., 2015, Lee et al., 2015, Ugrankar et al., 2015, Vedanayagam and Garrigan, 2015, Flici et al., 2014, Rogers et al., 2014, Yan et al., 2014, Czech et al., 2013, de Celis et al., 2013.9.11, Ghezzi et al., 2013, Neumüller et al., 2013, Tögel et al., 2013, Vaque et al., 2013, Yamamoto et al., 2013-, Bodai et al., 2012, Busser et al., 2012, Hainaut et al., 2012, Hilgers et al., 2012, Japanese National Institute of Genetics, 2012.5.21, Legent et al., 2012, Popkova et al., 2012, Zhai et al., 2012, Hilgers et al., 2011, Kirilly et al., 2011, Smolik, 2011.2.28, Toku et al., 2011, He et al., 2010, Pospisilik et al., 2010, Sela et al., 2010, Smolik, 2010.11.15, Stofanko et al., 2010, Ayroles et al., 2009, Dworkin et al., 2009, Stofanko et al., 2008, Straub et al., 2008, Gilfillan et al., 2007, Grieder et al., 2007, Grieder et al., 2007, Hung et al., 2007, Li et al., 2007, Lilja et al., 2007, Nagraj et al., 2007, Smolik and Jones, 2007, Weber et al., 2007, Friedman and Perrimon, 2006, DasGupta et al., 2005, Huen and Chan, 2005, Laviolette et al., 2005, Ito et al., 2004, Stanyon et al., 2004, Takeyama et al., 2004, Petruk et al., 2001)
    Name Synonyms
    Secondary FlyBase IDs
    • FBgn0015624
    • FBgn0030149
    • FBgn0066809
    • FBgn0028319
    • FBgn0027307
    • FBgn0040152
    • FBgn0030150
    Datasets (1)
    Study focus (1)
    Experimental Role
    Project
    Project Type
    Title
    • bait_protein
    Genome-wide localization of chromatin factors by ChIP-chip and ChIP-Seq.
    Study result (0)
    Result
    Result Type
    Title
    External Crossreferences and Linkouts ( 102 )
    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/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
    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
    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
    KEGG Pathways - A collection of manually drawn pathway maps representing knowledge of molecular interaction, reaction and relation networks.
    MIST (genetic) - An integrated Molecular Interaction Database
    MIST (protein-protein) - An integrated Molecular Interaction Database
    Reactome Metabolic Pathways - An open-source, open access, manually curated and peer-reviewed metabolic pathway database.
    SignaLink - A signaling pathway resource with multi-layered regulatory networks.
    References (412)