FB2025_01 , released February 20, 2025
Gene: Dmel\Rel
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General Information
Symbol
Dmel\Rel
Species
D. melanogaster
Name
Relish
Annotation Symbol
CG11992
Feature Type
FlyBase ID
FBgn0014018
Gene Model Status
Stock Availability
Gene Summary
Relish (Rel) encodes a transcription factor and the downstream component of the immune deficiency pathway, which regulates the antibacterial response and other less characterized cellular processes. [Date last reviewed: 2019-03-14] (FlyBase Gene Snapshot)
Also Known As

NF-κB, ird4, NFκB, l(3)neo36, Rel1

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
3-48
RefSeq locus
NT_033777 REGION:9044183..9047977
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 (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 (26 terms)
Terms Based on Experimental Evidence (25 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
involved_in immune response
inferred from mutant phenotype
inferred from expression pattern
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 genetic interaction with FLYBASE:brm; FB:FBgn0000212
inferred from genetic interaction with FLYBASE:mor; FB:FBgn0002783
inferred from direct assay
Terms Based on Predictions or Assertions (1 term)
CV Term
Evidence
References
Cellular Component (4 terms)
Terms Based on Experimental Evidence (4 terms)
CV Term
Evidence
References
Terms Based on Predictions or Assertions (1 term)
CV Term
Evidence
References
located_in cytoplasm
inferred from electronic annotation with InterPro:IPR000451
Protein Family (UniProt)
-
Summaries
Gene Snapshot
Relish (Rel) encodes a transcription factor and the downstream component of the immune deficiency pathway, which regulates the antibacterial response and other less characterized cellular processes. [Date last reviewed: 2019-03-14]
Gene Group (FlyBase)
NUCLEAR FACTOR - KAPPA B -
The NF-κB transcription factor family share an N-terminal Rel homology domain. NF-κB transcription factors play a major role in development and immunity. (Adapted from FBrf0155649 and FBrf0210750).
NUCLEAR FACTOR - KAPPA B INHIBITOR FAMILY -
The activity of NF-κB transcription factors is regulated by interaction with inhibitory IκB proteins. IκB family members are characterized by multiple ankyrin repeat regions through which they bind Rel homology domain of NF-κB transcription factors. (Adapted from FBrf0233452.)
Pathway (FlyBase)
Negative Regulators of JAK-STAT Signaling Pathway -
Negative regulators of JAK-STAT signaling down-regulate the pathway, attenuating transcriptional control by Stat92E.
Imd Signaling Pathway Core Components -
The immune deficiency (Imd) pathway primarily mediates the humoral immune response to Gram-negative bacteria. Activation of the Imd pathway by diaminopimelic acid-type peptidoglycan initiates a signaling cascade that ultimately results in the release of the NFκB-like factor Rel from auto-inhibition and its translocation into the nucleus to activate the transcription of antimicrobial peptides. (Adapted from FBrf0224587 and FBrf0238555.)
cGAS-STING Signaling Pathway Core Components -
The cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway is an anti-viral pattern recognition pathway. In Drosophila, cyclic GMP-AMP (cGAMP) synthases are activated by viral infection, cGAMP is in turn detected by STING ultimately resulting in the activation the NF-κB-like factor Rel and its translocation into the nucleus to activate the transcription of anti-viral genes. (Adapted from FBrf0252868.)
Protein Function (UniProtKB)
Transcription factor that plays a key role in the humoral immune response as part of the peptidoglycan recognition protein (IMD) signaling pathway (PubMed:10619029, PubMed:11269501, PubMed:11872802, PubMed:22022271, PubMed:29924997, PubMed:8816802). Rel-p68 subunit translocates to the nucleus where it binds to the promoter of the Cecropin A1 gene and probably other antimicrobial peptide genes (PubMed:11269501, PubMed:29924997). I-kappa-B kinase complex (IKKbeta and key) and PGRP-LC are essential signaling components in transmitting the lipopolysaccharide (LPS) signal leading to cact degradation for NF-kappa-B (rel) activation (PubMed:11018014, PubMed:11872802). Part of a Toll-related receptor pathway that functions in the apoptosis of unfit cells during cell competition (PubMed:25477468). Also part of some antiviral immunity: activated downstream of Sting signaling, which detects double-stranded RNA (dsRNA) from viruses, and promotes expression of antiviral effector genes (PubMed:29934091, PubMed:30119996, PubMed:33262294, PubMed:34261127, PubMed:34261128). May be part of a NF-kappa-B and Tollo signaling cascade that regulates development of the peripheral nervous system (PubMed:18000549). Possibly post-transcriptionally regulates the neuron-specific genes sc and ase, by promoting the rapid turnover of their transcripts in the wing imaginal disk (PubMed:18000549).
(UniProt, Q94527)
Summary (Interactive Fly)

Ankyrin-repeat and NFkappaB domain protein - a key factor in the induction of the humoral immune response in Drosophila, including antibacterial as well as antifungal factors - Relish acts in the IMD pathway

Gene Model and Products
Number of Transcripts
4
Number of Unique Polypeptides
2

Please see the JBrowse view of Dmel\Rel 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 Q94527)

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 5.48

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0089338
3499
971
FBtr0089339
3351
971
FBtr0089340
3042
971
FBtr0089341
2722
859
Additional Transcript Data and Comments
Reported size (kB)

3.5, 3.4, 3.1, 2.7 (northern blot)

3.4, 3.1, 2.7 (northern blot)

Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
UniProt
RefSeq ID
GenBank
FBpp0088375
109.8
971
6.49
FBpp0088973
109.8
971
6.49
FBpp0088971
109.8
971
6.49
FBpp0088972
97.9
859
6.54
Polypeptides with Identical Sequences

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

971 aa isoforms: Rel-PA, Rel-PB, Rel-PC
Additional Polypeptide Data and Comments
Reported size (kDa)
Comments
External Data
Subunit Structure (UniProtKB)

Rel-p68 subunit interacts with Dredd (PubMed:11269502). Interacts with DMAP1 (PubMed:24947515). Interacts with akirin; interaction is immune stimulation-dependent; activates selected rel target gene promoters (PubMed:25180232).

(UniProt, Q94527)
Post Translational Modification

Phosphorylated by lipopolysaccharide (LPS)-activated I-kappa-B kinase complex before being cleaved. Rel-p110 subunit is cleaved within seconds of an immune challenge into Rel-p49 subunit and Rel-p68 subunit. Rel-p110 subunit reappears after 45 minutes.

(UniProt, Q94527)
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\Rel 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).

-1.58

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

Rel expression in salivary glands begins 8 hours prior to puparium formation, and ends 12 hours after puparium formation, with a peak 2 hours APF.

3.4kb Rel transcripts are expressed constitutively and are induced about 15-fold upon infection.

The 3.1kb Rel transcripts are undetectable in untreated flies and are induced greater than 50-fold in infected flies.

A 2.7kb Rel transcript is present in early embryos and uninjected adult females.

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
Expression Deduced from Reporters
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\Rel 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) 1-3
  • 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 ( 20 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 46 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of Rel
Transgenic constructs containing regulatory region of Rel
Aberrations (Deficiencies and Duplications) ( 2 )
Inferred from experimentation ( 2 )
Gene disrupted in
Inferred from location ( 7 )
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
Orthologs
Human Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Homo sapiens (Human) (40)
10 of 14
Yes
Yes
10 of 14
Yes
Yes
3 of 14
No
No
3877  
3 of 14
No
No
1  
3 of 14
No
No
2 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 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
6  
1 of 14
No
No
1  
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
Yes
1 of 14
No
Yes
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 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) (29)
10 of 14
Yes
Yes
6 of 14
No
Yes
3 of 14
No
No
3 of 14
No
No
3 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
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
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Mus musculus (laboratory mouse) (31)
10 of 14
Yes
Yes
9 of 14
No
Yes
1  
3 of 14
No
No
1  
3 of 14
No
No
3 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
Yes
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Xenopus tropicalis (Western clawed frog) (18)
8 of 13
Yes
Yes
8 of 13
Yes
Yes
7 of 13
No
Yes
3 of 13
No
No
3 of 13
No
No
3 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
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
Danio rerio (Zebrafish) (37)
11 of 14
Yes
Yes
7 of 14
No
Yes
3 of 14
No
No
3 of 14
No
No
3 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
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
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) (7)
2 of 14
Yes
Yes
2 of 14
Yes
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
Anopheles gambiae (African malaria mosquito) (14)
9 of 12
Yes
Yes
2 of 12
No
No
Arabidopsis thaliana (thale-cress) (14)
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
Yes
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:Rel. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Drosophila melanogaster (Fruit fly) (12)
4 of 13
4 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
Human Disease Associations
FlyBase Human Disease Model Reports
    Disease Ontology (DO) Annotations
    Models Based on Experimental Evidence ( 2 )
    Potential Models Based on Orthology ( 2 )
    Modifiers Based on Experimental Evidence ( 10 )
    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
    esyN Network Diagram
    Show neighbor-neighbor interactions:
    Show/hide secondary interactors 
    (data from AllianceMine provided by esyN)
    Select Layout:
    Legend:
    Protein
    RNA
    Selected Interactor(s)
    Other 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
    esyN Network Diagram
    Show/hide secondary interactors 
    (data from AllianceMine provided by esyN)
    esyN Network Key:
    Suppression
    Enhancement
    Other 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)
    Rel-p68 subunit interacts with Dredd (PubMed:11269502). Interacts with DMAP1 (PubMed:24947515). Interacts with akirin; interaction is immune stimulation-dependent; activates selected rel target gene promoters (PubMed:25180232).
    (UniProt, Q94527 )
    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
    Class of Gene
    Genomic Location and Detailed Mapping Data
    Chromosome (arm)
    3R
    Recombination map
    3-48
    Cytogenetic map
    Sequence location
    FlyBase Computed Cytological Location
    Cytogenetic map
    Evidence for location
    85C3-85C3
    Limits computationally determined from genome sequence between P{lacW}l(3)L4740L4740 and P{EP}D1EP473
    Experimentally Determined Cytological Location
    Cytogenetic map
    Notes
    References
    85C9-85C10
    (determined by in situ hybridisation)
    85C1-85C13
    (determined by in situ hybridisation)
    85C-85C
    (determined by in situ hybridisation)
    Experimentally Determined Recombination Data
    Notes
    Stocks and Reagents
    Stocks (31)
    Genomic Clones (17)
     

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

    cDNA Clones (77)
     

    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
    Laboratory Generated Antibodies
    Commercially Available Antibodies
     
    Developmental Studies Hybridoma Bank - Monoclonal antibodies for use in research
    Cell Line Information
    Publicly Available Cell Lines
     
      Other Stable Cell Lines
       
      Other Comments

      Rel is necessary to provide immunity to reactive oxygen species-resistant pathogens.

      RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a specific decrease in AttA activity in response to heat-killed E.coli, and a reduction of Drs response via the Tl pathway, when assayed in S2 cells.

      dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.

      Rel endoproteolysis appears to be carried out by the caspase Dredd.

      Area matching Drosophila relish gene (inverted), Acc No. U62005.

      Mutants show no detectable induction of Dpt, CecA1 and CecA2. Attacin levels are reduced compared to wild type and Drs induction is normal.

      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.

      Identification: as a mutation that fails to induce expression of Ecol\lacZDpt.PR normally in response to infection. 4 "ird4" alleles have been obtained.

      The Rel protein is rapidly cleaved into two parts after immune challenge. An N-terminal fragment, containing the DNA-binding Rel homology domain, translocates to the nucleus, while the C-terminal IκB-like fragment remains in the cytoplasm.

      Identification: EMS screen for mutations that prevent Dpt expression in response to infection.

      Mutants exhibit a block of Dif nuclear localisation in response to infection.

      Rel is required for the signal-dependent localisation of Dif and has a less important or indirect role in nuclear localisation of dl.

      Rel encodes a protein containing both a rel homology domain and an IκB-like domain. Rel is strongly induced in infected flies, and a Rel transcript is also detected in early embryos. Rel can activate transcription from the CecA1 promoter of a CecA1-Ecol\lacZ reporter construct.

      Identified in a PCR differential display screen for genes induced when the immune system is activated.

      Relationship to Other Genes
      Source for database merge of

      Source for merge of: Rel l(3)neo36

      Source for merge of: Rel ird4

      Additional comments
      Nomenclature History
      Source for database identify of
      Nomenclature comments
      Etymology
      Synonyms and Secondary IDs (24)
      Reported As
      Symbol Synonym
      Rel
      (Balakireva et al., 2024, De Groef et al., 2024, Hachfi et al., 2024, Hersperger et al., 2024, Hu et al., 2024, Jeong, 2024, Kodra et al., 2024, Li et al., 2024, Lu et al., 2024, Mpamhanga and Kounatidis, 2024, Prakash et al., 2024, Rommelaere et al., 2024, Shan et al., 2024, Sharmin et al., 2024, Vesala et al., 2024, Wang et al., 2024, Wang et al., 2024, Wang et al., 2024, Zhang et al., 2024, Zhou et al., 2024, Zhou et al., 2024, Aalto et al., 2023, Aida et al., 2023, Bastin and Eleftherianos, 2023, Bland, 2023, Burghardt et al., 2023, Chen et al., 2023, He et al., 2023, Hsieh and Chiang, 2023, Keith, 2023, Mannino et al., 2023, Mirzoyan et al., 2023, Muita and Baxter, 2023, Pandey et al., 2023, Snee et al., 2023, Stączek et al., 2023, Titus et al., 2023, Touré et al., 2023, Wang et al., 2023, Yao et al., 2023, Zheng et al., 2023, Zhou and Boutros, 2023, Aggarwal et al., 2022, Carboni et al., 2022, Charroux and Royet, 2022, Chen et al., 2022, Davis et al., 2022, Deshpande et al., 2022, Ding et al., 2022, Hanson et al., 2022, Kim et al., 2022, Koranteng et al., 2022, Liu et al., 2022, Liu et al., 2022, Lu and Chtarbanova, 2022, Pavlidaki et al., 2022, Shen et al., 2022, Tendulkar et al., 2022, Valanne et al., 2022, Wang et al., 2022, Waring et al., 2022, Wu et al., 2022, Xiong et al., 2022, Zhou et al., 2022, Ahmed-Braimah et al., 2021, Beňová-Liszeková et al., 2021, Buhlman et al., 2021, Cattenoz et al., 2021, Fabian et al., 2021, Ferguson et al., 2021, Gan et al., 2021, Hanson et al., 2021, Hsieh et al., 2021, Marra et al., 2021, Mishra et al., 2021, Park et al., 2021, Parra-Peralbo et al., 2021, Salem Wehbe et al., 2021, Tang et al., 2021, Wagner et al., 2021, Cai et al., 2020, Cho et al., 2020, Deng et al., 2020, Han et al., 2020, Hung et al., 2020, Jasper, 2020, Jeon et al., 2020, Karageorgiou et al., 2020, Khor and Cai, 2020, Krautz et al., 2020, Lim et al., 2020, Rust et al., 2020, Swanson et al., 2020, Aalto et al., 2019, Araki et al., 2019, Carty and Bowie, 2019, Chaudhary and Boutros, 2019, Chen et al., 2019, Chowdhury et al., 2019, Engel et al., 2019, Fahey-Lozano et al., 2019, Hanson et al., 2019, Houtz et al., 2019, Khan et al., 2019, Lang et al., 2019, Lin et al., 2019, Maitra et al., 2019, Melcarne et al., 2019, Meltzer et al., 2019, Sanchez Bosch et al., 2019, Shokri et al., 2019, Shukla et al., 2019, Si et al., 2019, Tang and Engström, 2019, Troha and Buchon, 2019, Wang et al., 2019, Westfall et al., 2019, Akishina et al., 2018, Anthoney et al., 2018, Bischof et al., 2018, Davie et al., 2018, Davis and Rebay, 2018, Gene Disruption Project members, 2018-, Goto et al., 2018, Harris et al., 2018, Kwon et al., 2018, Li et al., 2018, Shibata and Kawabata, 2018, Steele et al., 2018, Troha et al., 2018, Yu et al., 2018, Akishina et al., 2017, Bastos et al., 2017, Christesen et al., 2017, Daisley et al., 2017, Dostálová et al., 2017, Keesey et al., 2017, Khadilkar et al., 2017, Kim et al., 2017, Kurz et al., 2017, Maki et al., 2017, Park et al., 2017, Romero-Pozuelo et al., 2017, Transgenic RNAi Project members, 2017-, Chatterjee et al., 2016, Di Gregorio et al., 2016, Guillou et al., 2016, Kučerová et al., 2016, Lamiable et al., 2016, Mistry et al., 2016, Baëza et al., 2015, Fan et al., 2015, Jasper, 2015, Kanoh et al., 2015, Li and Dijkers, 2015, Liu et al., 2015, Ma et al., 2015, model organism Encyclopedia of Regulatory Network (modERN) Project, 2015-, Sansone et al., 2015, Schertel et al., 2015, Sudmeier et al., 2015, Vedanayagam and Garrigan, 2015, Verma and Tapadia, 2015, Xia et al., 2015, Xiao et al., 2015, Zhang et al., 2015, Binggeli et al., 2014, Bonnay et al., 2014, Chen et al., 2014, Engel et al., 2014, Goto et al., 2014, Guo et al., 2014, Kuo and Williams, 2014, Kuo and Williams, 2014, Terhzaz et al., 2014, Aparicio et al., 2013, Ayyaz and Jasper, 2013, Buchon et al., 2013, Christofi and Apidianakis, 2013, Clark et al., 2013, Dantoft et al., 2013, Fukuyama et al., 2013, Gendrin et al., 2013, Huang et al., 2013, Iyer et al., 2013, Kari et al., 2013, Katzenberger et al., 2013, Petersen et al., 2013, Sen et al., 2013, Sen et al., 2013, Short and Lazzaro, 2013, Shravage et al., 2013, Spokony and White, 2013.5.10, Stefanatos et al., 2013, Zhang et al., 2013, An et al., 2012, Berger et al., 2012, Japanese National Institute of Genetics, 2012.5.21, Liu et al., 2012, Pilátová and Dionne, 2012, Rincon-Arano et al., 2012, Vanha-Aho et al., 2012, Wu et al., 2012, Clark et al., 2011, Narbonne-Reveau et al., 2011, Paredes et al., 2011, Zaidman-Rémy et al., 2011, Zhang and Arnosti, 2011, Zhao et al., 2011, Becker et al., 2010, Blanco et al., 2010, Buechling et al., 2010, Chen et al., 2010, Hill-Burns and Clark, 2010, Kong et al., 2010, Kuo et al., 2010, Matova and Anderson, 2010, Tanji et al., 2010, Tsuda et al., 2010, Buchon et al., 2009, Buchon et al., 2009, Buchon et al., 2009, Defaye et al., 2009, Dijkers and O'Farrell, 2009, Gendrin et al., 2009, Ha et al., 2009, Ha et al., 2009, Ha et al., 2009, Harbison et al., 2009, Helenius et al., 2009, Jin et al., 2009, Prokupek et al., 2009, Wiklund et al., 2009, Aggarwal et al., 2008, Boltz and Carney, 2008, Choi et al., 2008, Davis et al., 2008, Goto et al., 2008, Jin et al., 2008, Lhocine et al., 2008, Linder et al., 2008, Ratnaparkhi and Courey, 2008, Ratnaparkhi et al., 2008, Vonkavaara et al., 2008, Xi et al., 2008, Yano et al., 2008, Yatsu et al., 2008, Ayyar et al., 2007, Bidla et al., 2007, Copley et al., 2007, Curtis et al., 2007, Dijkers and O'Farrell, 2007, Junell et al., 2007, Kim et al., 2007, Kuranaga and Miura, 2007, Sackton et al., 2007, Valanne et al., 2007, Weiler, 2007, Bergmann, 2006, Brun et al., 2006, Kambris et al., 2006, Kambris et al., 2006, Kim et al., 2006, Libert et al., 2006, Liehl et al., 2006, Matova and Anderson, 2006, Scherfer et al., 2006, Zaidman-Remy et al., 2006, Gesellchen et al., 2005, Kim et al., 2005, Lee et al., 2005, McGettigan et al., 2005, Thoetkiattikul et al., 2005, Yagi and Ip, 2005, Lau et al., 2003, Uvell and Engstrom, 2003, Cornwell and Kirkpatrick, 2001, Gim et al., 2001, Dushay et al., 1996)
      Name Synonyms
      Nuclear Factor-kappa-B p110
      Nuclear factor NF-kappa-B p110 subunit
      Relish
      (Arias-Rojas et al., 2024, Asgari et al., 2024, Baek et al., 2024, Huang et al., 2024, Krejčová et al., 2024, Nigg et al., 2024, Rai and Bergmann, 2024, Wang et al., 2024, Wang et al., 2024, Arias-Rojas et al., 2023, Chen et al., 2023, Elguero et al., 2023, Joshi et al., 2023, Khan et al., 2023, Kietz and Meinander, 2023, Li et al., 2023, Meng et al., 2023, Mouawad et al., 2023, Pan et al., 2023, Robert et al., 2023, Tafesh-Edwards and Eleftherianos, 2023, Wang et al., 2023, Williams et al., 2023, Bahuguna et al., 2022, Barati et al., 2022, Benoit et al., 2022, Cammarata-Mouchtouris et al., 2022, Cheung et al., 2022, Ciesielski et al., 2022, Davis et al., 2022, Eleftherianos and Tafesh-Edwards, 2022, Goodman and Bellen, 2022, Liegeois and Ferrandon, 2022, Li et al., 2022, Nayak and Mishra, 2022, Neophytou and Pitsouli, 2022, Singh and Tapadia, 2022, Yu et al., 2022, Akkouche et al., 2021, Eleftherianos and Heryanto, 2021, Kanoh et al., 2021, Maitra et al., 2021, Montanari and Royet, 2021, Ozakman and Eleftherianos, 2021, Schneider and Imler, 2021, Slavik et al., 2021, Song et al., 2021, Wang et al., 2021, Zhu et al., 2021, Zulazmi et al., 2021, Arora and Ligoxygakis, 2020, Blount et al., 2020, Han et al., 2020, Hill et al., 2020, Iwashita et al., 2020, Lee et al., 2020, Ma et al., 2020, Makhnovskii et al., 2020, Masuzzo et al., 2020, Ramond et al., 2020, Rodriguez-Fernandez et al., 2020, Shaposhnikov et al., 2020, Tafesh-Edwards and Eleftherianos, 2020, Toprak et al., 2020, Zhang et al., 2020, Zugasti et al., 2020, Chen et al., 2019, Chen et al., 2019, Chowdhury et al., 2019, Dudzic et al., 2019, Valanne et al., 2019, Wang et al., 2019, Badinloo et al., 2018, Cara et al., 2018, Goto et al., 2018, Hori et al., 2018, Kounatidis and Chtarbanova, 2018, Losada-Perez, 2018, Ly et al., 2018, Min and Tatar, 2018, Palmer et al., 2018, Shahrestani et al., 2018, Sherri et al., 2018, Su et al., 2018, Westfall et al., 2018, Yuan et al., 2018, Zhai et al., 2018, Allada et al., 2017, Keita et al., 2017, Kenmoku et al., 2017, Kounatidis et al., 2017, Kurz et al., 2017, Liu et al., 2017, Maki et al., 2017, Mussabekova et al., 2017, Tavignot et al., 2017, Yadav et al., 2017, Ji et al., 2016, Kaynar et al., 2016, Kumar et al., 2016, Lim and Tsuda, 2016, Troutwine et al., 2016, Yadav and Tapadia, 2016, Yadav et al., 2016, Bandarra et al., 2015, Castillo et al., 2015, Kanoh et al., 2015, Li and Dijkers, 2015, Liu et al., 2015, Liu et al., 2015, Momiuchi et al., 2015, Shirinian et al., 2015, Stratoulias and Heino, 2015, Terhzaz et al., 2015, Vedanayagam and Garrigan, 2015, Yu et al., 2015, Bonnay et al., 2014, Goto et al., 2014, Imler, 2014, Keebaugh and Schlenke, 2014, Kim et al., 2014, Kleino and Silverman, 2014, Lee and Lee, 2014, Lindsay and Wasserman, 2014, Myllymäki et al., 2014, Panayidou et al., 2014, Tan et al., 2014, Terhzaz et al., 2014, Verma and Tapadia, 2014, Xu and Cherry, 2014, Aparicio et al., 2013, Cao et al., 2013, Clark et al., 2013, Dantoft et al., 2013, Ferrandon, 2013, Fukuyama et al., 2013, Kemp et al., 2013, Kingsolver et al., 2013, Luo et al., 2013, Owusu-Ansah et al., 2013, Shravage et al., 2013, Wang et al., 2013, An et al., 2012, Bitra et al., 2012, Bosco-Drayon et al., 2012, Felix et al., 2012, Jones et al., 2012, Meinander et al., 2012, Overend et al., 2012, Tsuzuki et al., 2012, Vandenabeele and Bertrand, 2012, Vanha-Aho et al., 2012, Verma and Tapadia, 2012, Wang et al., 2012, Akhouayri et al., 2011, Fullaondo et al., 2011, Garcia and Stathopoulos, 2011, Karpac et al., 2011, Marcu et al., 2011, Narbonne-Reveau et al., 2011, Ragab et al., 2011, Sehgal and Mignot, 2011, van Uden et al., 2011, Zaidman-Rémy et al., 2011, Becker et al., 2010, Kallio et al., 2010, Kuo et al., 2010, O'Callaghan and Vergunst, 2010, Radyuk et al., 2010, Ryu et al., 2010, Sabin et al., 2010, Tanji et al., 2010, Valanne et al., 2010, Berkey et al., 2009, Buchon et al., 2009, Defaye et al., 2009, Diangelo et al., 2009, Dijkers and O'Farrell, 2009, Ertürk-Hasdemir et al., 2009, Gendrin et al., 2009, Geuking et al., 2009, Ha et al., 2009, Harbison et al., 2009, Helenius et al., 2009, Jin et al., 2009, Liu et al., 2009, Obbard et al., 2009, Towb et al., 2009, Wiklund et al., 2009, Aggarwal et al., 2008, Choi et al., 2008, Davis et al., 2008, Goto et al., 2008, Hernandez-Romano et al., 2008, Jin et al., 2008, Jones et al., 2008, Kleino et al., 2008, Krupinski et al., 2008, Lhocine et al., 2008, Maillet et al., 2008, Orr et al., 2008, Pal et al., 2008, Ratnaparkhi and Courey, 2008, Ratnaparkhi et al., 2008, Reed et al., 2008, Ryu et al., 2008, Sekiya et al., 2008, Silverman et al., 2008, Tsai et al., 2008, Vonkavaara et al., 2008, Xi et al., 2008, Yano et al., 2008, Ayyar et al., 2007, Busse et al., 2007, Copley et al., 2007, Dijkers and O'Farrell, 2007, Huh et al., 2007, Kim et al., 2007, Levine and Begun, 2007, Libert et al., 2007, Minidorff et al., 2007, Sackton et al., 2007, Valanne et al., 2007, Waterhouse et al., 2007, Williams et al., 2007, Wu and Silverman, 2007, Wu et al., 2007, Akira et al., 2006, Brun et al., 2006, Delaney et al., 2006, Kim et al., 2006, Kim et al., 2006, Leulier et al., 2006, Libert et al., 2006, Liehl et al., 2006, Matova and Anderson, 2006, Minakhina and Steward, 2006, Ryu et al., 2006, Saleh et al., 2006, Scherfer et al., 2006, Senger et al., 2006, Gesellchen et al., 2005, Greene et al., 2005, Kim et al., 2005, Lee et al., 2005, Wertheim et al., 2005, Yagi and Ip, 2005, Bettencourt et al., 2004, Roxstrom-Lindquist et al., 2004, Ryu et al., 2004, Cha et al., 2003, Minakhina et al., 2003, Park et al., 2003, Uvell and Engstrom, 2003, Yajima et al., 2003, Avila et al., 2002, Bhattacharya and Steward, 2002, Lehmann et al., 2002, Roxstrom-Lindquist et al., 2002, Gim et al., 2001, Lindmark et al., 2001, Silverman et al., 2000, Asling, 1999.9.13, Hedengren, 1999.9.14, Hedengren, 1999.9.14, Hedengren, 1999.9.14, Hedengren, 1999.9.14, Hedengren, 1999.9.14, Hedengren, 1999.9.14, Dushay et al., 1997, Dushay, 1996.6.24, Dushay et al., 1996, Hultmark, 1995.6.7)
      immune response deficient 4
      Secondary FlyBase IDs
      • FBgn0011469
      • FBgn0024223
      Datasets (0)
      Study focus (0)
      Experimental Role
      Project
      Project Type
      Title
      Study result (0)
      Result
      Result Type
      Title
      External Crossreferences and Linkouts ( 106 )
      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
      Developmental Studies Hybridoma Bank - Monoclonal antibodies for use in research
      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 (genetic) - An integrated Molecular Interaction Database
      MIST (protein-protein) - An integrated Molecular Interaction Database
      SignaLink - A signaling pathway resource with multi-layered regulatory networks.
      References (906)