FB2024_03 , released June 25, 2024
Gene: Dmel\fng
Open Close
General Information
Symbol
Dmel\fng
Species
D. melanogaster
Name
fringe
Annotation Symbol
CG10580
Feature Type
FlyBase ID
FBgn0011591
Gene Model Status
Stock Availability
Enzyme Name (EC)
O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase (2.4.1.222)
Gene Summary
fringe (fng) encodes a glycosyltransferase that modifies EGF domains of the product of N. This glycosylation enhances the interactions the product of N with its ligand encoded by Delta, and inhibits those with its ligand encoded by Ser. In this way the product of fng modulates Notch signaling. [Date last reviewed: 2019-03-07] (FlyBase Gene Snapshot)
Also Known As

l(3)rG554

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
3-47
RefSeq locus
NT_037436 REGION:20925891..20949512
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 (1 term)
Terms Based on Experimental Evidence (1 term)
CV Term
Evidence
References
Terms Based on Predictions or Assertions (1 term)
CV Term
Evidence
References
Biological Process (18 terms)
Terms Based on Experimental Evidence (16 terms)
CV Term
Evidence
References
inferred from direct assay
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 direct assay
inferred from mutant phenotype
inferred from genetic interaction with FLYBASE:Ser; FB:FBgn0004197
inferred from mutant phenotype
inferred from mutant phenotype
inferred from direct assay
Terms Based on Predictions or Assertions (2 terms)
CV Term
Evidence
References
inferred from electronic annotation with InterPro:IPR017374
inferred from biological aspect of ancestor with PANTHER:PTN000087518
Cellular Component (6 terms)
Terms Based on Experimental Evidence (5 terms)
CV Term
Evidence
References
located_in cytoplasm
inferred from high throughput direct assay
inferred from direct assay
located_in Golgi apparatus
inferred from direct assay
inferred from direct assay
located_in Golgi stack
inferred from direct assay
Terms Based on Predictions or Assertions (1 term)
CV Term
Evidence
References
located_in Golgi membrane
inferred from electronic annotation with InterPro:IPR017374
Protein Family (UniProt)
Belongs to the glycosyltransferase 31 family. (Q24342)
Catalytic Activity (EC/Rhea)
O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase activity
(1) 3-O-(alpha-L-fucosyl)-L-seryl-[EGF-like domain protein] + UDP-N- acetyl-alpha-D-glucosamine = 3-O-(N-acetyl-beta-D-glucosaminyl-(1->3)- alpha-L-fucosyl)-L-seryl-[EGF-like domain protein] + H(+) + UDP (2.4.1.222)
(2) 3-O-(alpha-L-fucosyl)-L-threonyl-[EGF-like domain protein] + UDP-N- acetyl-alpha-D-glucosamine = 3-O-(N-acetyl-beta-D-glucosaminyl-(1->3)- alpha-L-fucosyl)-L-threonyl-[EGF-like domain protein] + H(+) + UDP (2.4.1.222)
Summaries
Gene Snapshot
fringe (fng) encodes a glycosyltransferase that modifies EGF domains of the product of N. This glycosylation enhances the interactions the product of N with its ligand encoded by Delta, and inhibits those with its ligand encoded by Ser. In this way the product of fng modulates Notch signaling. [Date last reviewed: 2019-03-07]
Pathway (FlyBase)
Positive Regulators of Notch Signaling Pathway -
The Notch receptor signaling pathway is activated by the binding of the transmembrane receptor Notch (N) to transmembrane ligands, Dl or Ser, presented on adjacent cells. This results in the proteolytic cleavage of N, releasing the intracellular domain (NICD). NICD translocates into the nucleus, interacting with Su(H) and mam to form a transcription complex, which up-regulates transcription of Notch-responsive genes. Positive regulators of the pathway enhance the signal from the sending cell or the response in the receiving cell. (Adapted from FBrf0225731 and FBrf0192604).
Negative Regulators of Notch Signaling Pathway -
The Notch receptor signaling pathway is activated by the binding of the transmembrane receptor Notch (N) to transmembrane ligands, Dl or Ser, presented on adjacent cells. This results in the proteolytic cleavage of N, releasing the intracellular domain (NICD). NICD translocates into the nucleus, interacting with Su(H) and mam to form a transcription complex, which up-regulates transcription of Notch-responsive genes. Negative regulators of the pathway down-regulate the signal from the sending cell or the response in the receiving cell. (Adapted from FBrf0225731 and FBrf0192604).
Gene Group (FlyBase)
BETA 1,3-N-ACETYLGLUCOSAMINYLTRANSFERASE -
Beta 1,3-N-acetylglucosaminyltransferase catalyze the transfer of N-acetylglucosamine (GlcNAc) in a beta-1,3 linkage to substrates including glycolipids and proteins.
Protein Function (UniProtKB)
Glycosyltransferase involved in the elongation of O-linked ligands to activate Notch signaling. Possesses fucose-specific beta-1,3-N-acetylglucosaminyltransferase activity; extends the O-linked fucose on the Notch EGF repeats. Boundary-specific cell-signaling molecule that is responsible for dorsal-ventral cell interactions during wing development.
(UniProt, Q24342)
Summary (Interactive Fly)

secreted glycosyltransferase involved boundary formation - Notch antagonist that functions by targeting extracellular domain of Notch - Chip and Beadex function antagonistically on Notch signaling through directly regulation of fringe transcription

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

Please see the JBrowse view of Dmel\fng 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 Q24342)

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

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

Gene model reviewed during 5.46

Gene model reviewed during 5.56

Sequence Ontology: Class of Gene
Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0078267
1959
412
Additional Transcript Data and Comments
Reported size (kB)

1.9 (northern blot)

Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
UniProt
RefSeq ID
GenBank
FBpp0077925
47.0
412
8.08
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
Crossreferences
InterPro - A database of protein families, domains and functional sites
Linkouts
Sequences Consistent with the Gene Model
Mapped Features

Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\fng 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).

-0.84

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

fng transcript is expressed 4-5 polar follicle cell precursor cells in stage 1-4 egg chambers, and later in the 2 polar cells that emerge from the prepolar group.

fng transcript is expressed in follicle cells starting in germarium region 2b. Expression is detected in anterior and posterior follicle cells in stage S2-S4, in all follicle cells in stage S5, in anterior and posterior polar follicle cells in stage S6-S9. At stage S10, expression is detected in all follicle cells except anterior-dorsal follicle cells.

fng is first detected in the wing disc in second instar larvae where it is restricted to the dorsal region of the disc. Expression remains in the dorsal part of the wing disc through the first half of the third instar after which some weak expression begins to appear in ventral regions outside of the wing pouch. In addition, fng expression is lost in some regions that will give rise to the notum. By the end of third instar, expression is lost in some dorsal regions within the wing pouch and becomes strong in proximal regions of the ventral wing.

Marker for
 
Subcellular Localization
CV Term
Polypeptide Expression
immunolocalization
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data

Epitope-tagged fng protein localizes to the Golgi apparatus.

Marker for
 
Subcellular Localization
CV Term
Evidence
References
located_in cytoplasm
inferred from high throughput direct assay
inferred from direct assay
located_in Golgi apparatus
inferred from direct assay
inferred from direct assay
located_in Golgi stack
inferred from direct assay
Expression Deduced from Reporters
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\fng 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) 9-10
  • Stages(s) 11-12
  • Stages(s) 13-16
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 45 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 23 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of fng
Transgenic constructs containing regulatory region of fng
Aberrations (Deficiencies and Duplications) ( 4 )
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
filamentous actin & denticle field primordium
leg & joint, with Scer\GAL4Dll-md23
Orthologs
Human Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Homo sapiens (Human) (9)
14 of 14
Yes
Yes
13 of 14
No
Yes
13 of 14
No
Yes
1  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Rattus norvegicus (Norway rat) (9)
14 of 14
Yes
Yes
13 of 14
No
Yes
13 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
Mus musculus (laboratory mouse) (9)
14 of 14
Yes
Yes
2  
13 of 14
No
Yes
2  
12 of 14
No
Yes
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
Xenopus tropicalis (Western clawed frog) (9)
11 of 13
Yes
Yes
6 of 13
No
Yes
6 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
Yes
1 of 13
No
No
Danio rerio (Zebrafish) (13)
13 of 14
Yes
Yes
13 of 14
Yes
Yes
12 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
Caenorhabditis elegans (Nematode, roundworm) (11)
2 of 14
Yes
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
Anopheles gambiae (African malaria mosquito) (6)
12 of 12
Yes
Yes
Arabidopsis thaliana (thale-cress) (13)
2 of 13
Yes
No
2 of 13
Yes
No
2 of 13
Yes
No
2 of 13
Yes
Yes
2 of 13
Yes
No
2 of 13
Yes
No
2 of 13
Yes
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) (0)
Schizosaccharomyces pombe (Fission yeast) (0)
Escherichia coli (enterobacterium) (0)
Other Organism Orthologs (via OrthoDB)
Data provided directly from OrthoDB:fng. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Drosophila melanogaster (Fruit fly) (13)
3 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
Human Disease Associations
FlyBase Human Disease Model Reports
    Disease Ontology (DO) Annotations
    Models Based on Experimental Evidence ( 0 )
    Allele
    Disease
    Evidence
    References
    Potential Models Based on Orthology ( 1 )
    Modifiers Based on Experimental Evidence ( 2 )
    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
    RNA-RNA
    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
    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)
    Positive Regulators of Notch Signaling Pathway -
    The Notch receptor signaling pathway is activated by the binding of the transmembrane receptor Notch (N) to transmembrane ligands, Dl or Ser, presented on adjacent cells. This results in the proteolytic cleavage of N, releasing the intracellular domain (NICD). NICD translocates into the nucleus, interacting with Su(H) and mam to form a transcription complex, which up-regulates transcription of Notch-responsive genes. Positive regulators of the pathway enhance the signal from the sending cell or the response in the receiving cell. (Adapted from FBrf0225731 and FBrf0192604).
    Negative Regulators of Notch Signaling Pathway -
    The Notch receptor signaling pathway is activated by the binding of the transmembrane receptor Notch (N) to transmembrane ligands, Dl or Ser, presented on adjacent cells. This results in the proteolytic cleavage of N, releasing the intracellular domain (NICD). NICD translocates into the nucleus, interacting with Su(H) and mam to form a transcription complex, which up-regulates transcription of Notch-responsive genes. Negative regulators of the pathway down-regulate the signal from the sending cell or the response in the receiving cell. (Adapted from FBrf0225731 and FBrf0192604).
    Metabolic Pathways
    KEGG Metabolic Pathways - A collection of manually drawn metabolic pathway maps representing knowledge of molecular interaction, reaction and relation networks.
    External Data
    Linkouts
    KEGG Pathways - A collection of manually drawn pathway maps representing knowledge of molecular interaction, reaction and relation networks.
    SignaLink - A signaling pathway resource with multi-layered regulatory networks.
    Genomic Location and Detailed Mapping Data
    Chromosome (arm)
    3L
    Recombination map
    3-47
    Cytogenetic map
    Sequence location
    FlyBase Computed Cytological Location
    Cytogenetic map
    Evidence for location
    78A1-78A1
    Limits computationally determined from genome sequence between P{EP}trblEP3519 and P{EP}fngEP3082&P{lacW}skdL7062
    Experimentally Determined Cytological Location
    Cytogenetic map
    Notes
    References
    78A1-78A2
    (determined by in situ hybridisation)
    78A-78A
    (determined by in situ hybridisation)
    Experimentally Determined Recombination Data
    Left of (cM)
    Right of (cM)
    Notes
    Stocks and Reagents
    Stocks (22)
    Genomic Clones (27)
    cDNA Clones (38)
     

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

      Glycosylation of the N protein domain 'EGF12' is necessary for fng to inhibit the activation of N signalling by Ser but is not necessary for Ser binding to N.

      fng is required via N activation od an ap dependent affinity difference at the dorsal ventral restriction boundary in the wing disc.

      Interacts genetically with 'eyeful' mutant though it is not yet clear whether 'eyeful' corresponds to lola or psq.

      fng plays a key role in positioning N activation during early oogenesis. fng is required cell-autonomously in the somatic polar cells for follicle formation and also for polar cell fate. fng is required non-autonomously to define the number and organization of stalk cells.

      The glycosyltransferase activity of fng modulates N-Dl interactions.

      fng seems to function in peripodial cells during eye development.

      fng and N form a complex through both the Lin-Notch repeats and the epidermal growth factor repeats 22-36.

      The glycosyltransferase activity of fng modifies N.

      fng does not exert its effect outside the cell, but rather acts in the golgi apparatus, apparently as a glycosyltransferase.

      fng is essential in oogenesis for the proper formation of the egg chamber and for epithelial morphogenesis.

      fng protein does not detectably affect the ligand-receptor interactions of the N pathway in cultured cells.

      Local activation of N is necessary and sufficient to promote the formation of joints between segments of the leg. This segmentation process requires the participation of Ser, Dl and fng.

      fng plays a key role in dorsal-ventral compartmentalization in the wing disc, primarily by positioning a stripe of N activation, but fng may also exert additional influences on compartmentalization.

      The boundary of fng expression in the developing eye, with the subsequent implications for N signalling, is crucial for the induction of dorso-ventral mirror symmetry and eye morphogenesis.

      The regulated expression pattern of fng is essential for eye growth and formation of the equator. Boundaries of fng expression determine where N will be activated.

      ap mediates cell interactions across the DV axis of the wing by regulating the expression of Ser and fng. In ap mutants the wing is lost, this phenotype can be rescued by ectopic expression of either Ser or fng and the resulting wings have both dorsal and ventral cell fates.

      Ser does not signal in the dorsal regions of the developing imaginal wing disc due to the action of the fng gene product. Ectopic expression studies reveal the regulation of Ser by fng occurs at the level of protein and not Ser transcription.

      fng can suppress the ability of SerBd-3 to antagonize Dl during neurogenesis.

      Ser and Dl maintain each other's expression in the wing by a positive feedback loop. fng functions to position and restrict this feedback loop to the developing dorsal-ventral boundary.

      fng and Ser are distinct components of a single ap-regulated cell recognition and signal induction mechanism. Clonal analysis demonstrates that fng serves as a boundary-determining molecule such that Ser is induced wherever cells expressing fng and cells not expressing fng are juxtaposed.

      fng encodes a boundary-specific cell-signalling molecule that is responsible for dorsal-ventral cell interactions during wing development.

      Relationship to Other Genes
      Source for database merge of

      Source for merge of: fng l(3)rG554

      Additional comments
      Nomenclature History
      Source for database identify of
      Nomenclature comments
      Etymology
      Synonyms and Secondary IDs (13)
      Reported As
      Symbol Synonym
      fng
      (Li et al., 2024, Pfefferkorn et al., 2024, Burghardt et al., 2023, Troost et al., 2023, Hayashi et al., 2022, Li et al., 2022, Wang et al., 2022, Everetts et al., 2021, Laurichesse and Soler, 2020, Yamamoto, 2020, Fic et al., 2019, Pandey et al., 2019, Zhang and Ten Hagen, 2019, Zhu et al., 2019, Hall et al., 2018, Yang and Deng, 2018, Court et al., 2017, Dai et al., 2017, Kojima, 2017, Lin et al., 2017, Han et al., 2016, Morimoto et al., 2016, Sarov et al., 2016, Barrios et al., 2015, Bieli et al., 2015, Ishio et al., 2015, Morozova et al., 2015, Spratford and Kumar, 2015, Tsai et al., 2015, Ashwal-Fluss et al., 2014, DeSalvo et al., 2014, LeBon et al., 2014, Luck et al., 2014, Tseng et al., 2014, Zacharioudaki and Bray, 2014, Da Ros et al., 2013, Webber et al., 2013, Yang et al., 2013, Zoranovic et al., 2013, Troost and Klein, 2012, Xu and Gridley, 2012, Cherbas et al., 2011, Slattery et al., 2011, Bronstein et al., 2010, Egger et al., 2010, Ishikawa et al., 2010, Liefke et al., 2010, Roignant et al., 2010, Stacey et al., 2010, Tajiri et al., 2010, Ayroles et al., 2009, Dworkin et al., 2009, Flaherty et al., 2009, Gutierrez-Aviño et al., 2009, Hurlbut et al., 2009, Lee et al., 2009, Tomoyasu et al., 2009, Aoki et al., 2008, Becam and Milán, 2008, Berger et al., 2008, Okajima et al., 2008, Beltran et al., 2007, Buceta et al., 2007, Cook, 2007.1.23, Cook, 2007.1.24, Grieder et al., 2007, Grueber et al., 2007, Kankel et al., 2007, Levine et al., 2007, Sato and Tomlinson, 2007, Thomas and van Meyel, 2007, Xu et al., 2007, Atkey et al., 2006, Terry et al., 2006, Althauser et al., 2005, Jordan et al., 2005, Mok et al., 2005, Pérez et al., 2005, Hall et al., 2004, Wang and Struhl, 2004, Lei et al., 2003, Delanoue et al., 2002)
      Name Synonyms
      β3-N-acetylglucosaminyltransferase
      Secondary FlyBase IDs
      • FBgn0011797
      Datasets (0)
      Study focus (0)
      Experimental Role
      Project
      Project Type
      Title
      Study result (0)
      Result
      Result Type
      Title
      External Crossreferences and Linkouts ( 44 )
      Sequence Crossreferences
      NCBI Gene - Gene integrates information from a wide range of species. A record may include nomenclature, Reference Sequences (RefSeqs), maps, pathways, variations, phenotypes, and links to genome-, phenotype-, and locus-specific resources worldwide.
      GenBank Nucleotide - A collection of sequences from several sources, including GenBank, RefSeq, TPA, and PDB.
      GenBank Protein - A collection of sequences from several sources, including translations from annotated coding regions in GenBank, RefSeq and TPA, as well as records from SwissProt, PIR, PRF, and PDB.
      RefSeq - A comprehensive, integrated, non-redundant, well-annotated set of reference sequences including genomic, transcript, and protein.
      UniProt/GCRP - The gene-centric reference proteome (GCRP) provides a 1:1 mapping between genes and UniProt accessions in which a single 'canonical' isoform represents the product(s) of each protein-coding gene.
      UniProt/Swiss-Prot - Manually annotated and reviewed records of protein sequence and functional information
      Other crossreferences
      AlphaFold DB - AlphaFold provides open access to protein structure predictions for the human proteome and other key proteins of interest, to accelerate scientific research.
      BDGP expression data - Patterns of gene expression in Drosophila embryogenesis
      DRscDB - A single-cell RNA-seq resource for data mining and data comparison across species
      EMBL-EBI Single Cell Expression Atlas - Single cell expression across species
      FlyAtlas2 - A Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data
      FlyMine - An integrated database for Drosophila genomics
      InterPro - A database of protein families, domains and functional sites
      KEGG Genes - Molecular building blocks of life in the genomic space.
      MARRVEL_MODEL - MARRVEL (model organism gene)
      Linkouts
      BioGRID - A database of protein and genetic interactions.
      Drosophila Genomics Resource Center - Drosophila Genomics Resource Center (DGRC) cDNA clones
      DroID - A comprehensive database of gene and protein interactions.
      DRSC - Results frm RNAi screens
      Eukaryotic Promoter Database - A collection of databases of experimentally validated promoters for selected model organisms.
      FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
      FlyCyc Genes - Genes from a BioCyc PGDB for Dmel
      Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
      Flygut - An atlas of the Drosophila adult midgut
      iBeetle-Base - RNAi phenotypes in the red flour beetle (Tribolium castaneum)
      Interactive Fly - A cyberspace guide to Drosophila development and metazoan evolution
      KEGG Metabolic Pathways - A collection of manually drawn metabolic pathway maps representing knowledge of molecular interaction, reaction and relation networks.
      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 (390)