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General Information
Symbol
Dmel\cnn
Species
D. melanogaster
Name
centrosomin
Annotation Symbol
CG4832
Feature Type
FlyBase ID
FBgn0013765
Gene Model Status
Stock Availability
Gene Snapshot
centrosomin (cnn) encodes an essential mitotic centrosome component. During early embryogenesis it is required to organize the mitotic spindle, the actin cytoskeleton and centriole replication. It is also required for mitotic and meiotic divisions during spermatogenesis, as well as organization of the sperm axoneme. The product of cnn can interact with microtubules, actin and the kinase encoded by polo. [Date last reviewed: 2019-05-23]
Also Known As
oblivious, mat(2)syn-C, obv
Key Links
Genomic Location
Cytogenetic map
Sequence location
2R:13,439,314..13,450,475 [-]
Recombination map
2-68
Sequence
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
GO Summary Ribbons
Protein Family (UniProt)
-
Molecular Function (GO)
[Detailed GO annotations]
Experimental Evidence
Predictions / Assertions
-
Summaries
Protein Function (UniProtKB)
Core component of the centrosome throughout spermatogenesis. May participate in mitotic spindle assembly and the mechanics of morphogenesis through an interaction with microtubules, either directly or indirectly. Is a target of several homeotic genes.
(UniProt, P54623)
Summary (Interactive Fly)
Gene Model and Products
Number of Transcripts
12
Number of Unique Polypeptides
10

Please see the GBrowse view of Dmel\cnn or the JBrowse view of Dmel\cnn 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
Comments on Gene Model
Gene model reviewed during 5.41
Multiphase exon postulated: exon reading frame differs in alternative transcripts; overlap >20aa.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.45
Tissue-specific extension of 3' UTRs observed during later stages (FBrf0218523, FBrf0219848); all variants may not be annotated
Sequence Ontology: Class of Gene
Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0087703
4322
1148
FBtr0087704
4621
1120
FBtr0100654
4140
1090
FBtr0100656
4651
1130
FBtr0301395
1709
480
FBtr0306635
1824
462
FBtr0309888
1769
500
FBtr0309889
4830
1320
FBtr0309890
2006
520
FBtr0309891
5012
1378
FBtr0309892
4399
1120
FBtr0309893
4310
1120
Additional Transcript Data and Comments
Reported size (kB)
5.0, 4.5, 4.3 (northern blot)
5.0, 4.8 (northern blot)
Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
RefSeq ID
GenBank
FBpp0086822
129.9
1148
5.01
FBpp0086823
126.8
1120
5.19
FBpp0100116
123.7
1090
5.29
FBpp0100117
128.0
1130
5.22
FBpp0290609
53.8
480
7.07
FBpp0297590
52.2
462
7.63
FBpp0301622
55.9
500
7.33
FBpp0301623
149.5
1320
5.97
FBpp0301624
58.4
520
6.02
FBpp0301625
155.7
1378
5.44
FBpp0301626
126.8
1120
5.19
FBpp0301627
126.8
1120
5.19
Polypeptides with Identical Sequences

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

1120 aa isoforms: cnn-PB, cnn-PM, cnn-PN
Additional Polypeptide Data and Comments
Reported size (kDa)
1106 (aa); 150, 120 (kD observed); 124 (kD predicted)
1033 (aa); 118 (kD predicted)
Comments
External Data
Subunit Structure (UniProtKB)
Monomer.
(UniProt, P54623)
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\cnn using the Feature Mapper tool.

External Data
Crossreferences
Eukaryotic Promoter Database - A collection of databases of experimentally validated promoters for selected model organisms.
Linkouts
Gene Ontology (16 terms)
Molecular Function (1 term)
Terms Based on Experimental Evidence (1 term)
CV Term
Evidence
References
inferred from physical interaction with FLYBASE:Sas-4; FB:FBgn0011020
inferred from physical interaction with FLYBASE:Cen; FB:FBgn0032876
Terms Based on Predictions or Assertions (0 terms)
Biological Process (11 terms)
Terms Based on Experimental Evidence (11 terms)
CV Term
Evidence
References
Terms Based on Predictions or Assertions (0 terms)
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
non-traceable author statement
Expression Data
Expression Summary Ribbons
Colored tiles in ribbon indicate that expression data has been curated by FlyBase for that anatomical location. Colorless tiles indicate that there is no curated data for that location.
For complete stage-specific expression data, view the modENCODE Development RNA-Seq section under High-Throughput Expression below.
Transcript Expression
in situ
Stage
Tissue/Position (including subcellular localization)
Reference
organism | ubiquitous

Comment: maternally deposited

northern blot
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data
cnn transcripts are first detected at stage 5. High levels are present in gastrulating embryos along the ventral and cephalic furrows and later in the mesoderm. By stage 10, expression is seen in neuroblasts of the CNS, and by stage 11 in the PNS. By stage 14, expression is stronger in the thoracic part of the nerve cord than in the abdominal region and can be seen in the brain hemispheres as well. From stage 11-16, expression is observed in two domains of the visceral mesoderm surrounding the midgut. Double labeling shows that the anterior domain is located just anterior to cells expressing Scr and the posterior domain overlaps with cells expressing Antp and Ubx.
Marker for
 
Subcellular Localization
CV Term
Polypeptide Expression
immunolocalization
Stage
Tissue/Position (including subcellular localization)
Reference
western blot
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data
cnn protein localizes to the centrosomes of the first zygotic nucleus. This centrosomal association persists throughout the 13 synchronous rounds of nuclear divisions of the syncytial embryo. During the syncytial divisions, cnn protein is found at all microtubule-organizing centers. The centrosome localization is not dependent on the presence of an intact microtubule cytoskeleton.
cnn protein is expressed at high levels during both mitotic and meiotic divisions. It is closely associated with the centrosomes in a cell-dependent manner throughout spermatogenesis. During spermatogonial cell mitoses, cnn protein is strongly detected at spindle poles. At interphases it is present in centrosomes at much lower levels and is found at high levels in the cytoplasm. During the rapid growth phase of primary spermatocytes, cnn protein is in close association with the centriole. In each spermatocyte, two dots of cnn staining are seen at the membrane, representing the duplicated centrosomes. Later, as cells approach the meiotic divisions, the centrosomes migrate back to the nuclear membranes and higher levels of cnn protein staining are seen in the centrosomes. Accumulation of FBgn0013765:cnn protein in the spermatocyte centrosomes is not dependent on the presence of microtubules. FBgn0013765:cnn protein is detected in the centrosomes during both meiotic divisions. During meiosis II, there is a single centriole in each centrosome. In postmeiotic cells, the single centriole inserts into the nucleus and becomes the basal body. FBgn0013765:cnn @ protein is detected in the basal body until the early stages of axonemal elongation.
The pattern of cnn protein distribution is essentially identical to that of cnn transcripts. Immunostaining demonstrates that there are more cells toward the ventral midline in the thoracic neuromeres that express cnn protein compared to the abdominal neuromeres. Furthermore, cnn protein and transcript expression patterns are not identical in the visceral mesoderm. cnn protein is not visible in the visceral mesoderm at late germ band retraction but is observed in stages 14-16 in the visceral mesoderm of the gastric caecae and the second midgut constriction.
Marker for
 
Subcellular Localization
CV Term
Evidence
References
Expression Deduced from Reporters
High-Throughput Expression Data
Associated Tools

GBrowse - Visual display of RNA-Seq signals

View Dmel\cnn in GBrowse 2
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
FLIGHT - Cell culture data for RNAi and other high-throughput technologies
FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
Flygut - An atlas of the Drosophila adult midgut
Images
Alleles, Insertions, and Transgenic Constructs
Classical and Insertion Alleles ( 23 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 26 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of cnn
Transgenic constructs containing regulatory region of cnn
Deletions and Duplications ( 9 )
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
centrosome & male germline stem cell
embryonic cortex & actin filament
male germline stem cell & centrosome
male germline stem cell & spindle
meiosis I & aster
spermatocyte & spindle
Orthologs
Human Orthologs (via DIOPT v7.1)
Homo sapiens (Human) (3)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
4 of 15
Yes
Yes
2 of 15
No
Yes
1 of 15
No
Yes
Model Organism Orthologs (via DIOPT v7.1)
Mus musculus (laboratory mouse) (3)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
4 of 15
Yes
Yes
2 of 15
No
Yes
1 of 15
No
No
Rattus norvegicus (Norway rat) (3)
2 of 13
Yes
Yes
1 of 13
No
No
1 of 13
No
Yes
Xenopus tropicalis (Western clawed frog) (5)
1 of 12
Yes
Yes
1 of 12
Yes
Yes
1 of 12
Yes
No
1 of 12
Yes
No
1 of 12
Yes
No
Danio rerio (Zebrafish) (4)
2 of 15
Yes
Yes
1 of 15
No
No
1 of 15
No
No
Caenorhabditis elegans (Nematode, roundworm) (0)
No records found.
Arabidopsis thaliana (thale-cress) (0)
No records found.
Saccharomyces cerevisiae (Brewer's yeast) (0)
No records found.
Schizosaccharomyces pombe (Fission yeast) (0)
No records found.
Orthologs in Drosophila Species (via OrthoDB v9.1) ( EOG09190105 )
Organism
Common Name
Gene
AAA Syntenic Ortholog
Multiple Dmel Genes in this Orthologous Group
Drosophila melanogaster
fruit fly
Drosophila suzukii
Spotted wing Drosophila
Drosophila simulans
Drosophila sechellia
Drosophila erecta
Drosophila yakuba
Drosophila ananassae
Drosophila pseudoobscura pseudoobscura
Drosophila persimilis
Drosophila willistoni
Drosophila virilis
Drosophila mojavensis
Drosophila grimshawi
Orthologs in non-Drosophila Dipterans (via OrthoDB v9.1) ( EOG0915044Z )
Organism
Common Name
Gene
Multiple Dmel Genes in this Orthologous Group
Musca domestica
House fly
Musca domestica
House fly
Glossina morsitans
Tsetse fly
Lucilia cuprina
Australian sheep blowfly
Mayetiola destructor
Hessian fly
Aedes aegypti
Yellow fever mosquito
Anopheles darlingi
American malaria mosquito
Anopheles gambiae
Malaria mosquito
Culex quinquefasciatus
Southern house mosquito
Culex quinquefasciatus
Southern house mosquito
Culex quinquefasciatus
Southern house mosquito
Orthologs in non-Dipteran Insects (via OrthoDB v9.1) ( EOG090W05GG )
Organism
Common Name
Gene
Multiple Dmel Genes in this Orthologous Group
Apis florea
Little honeybee
Apis mellifera
Western honey bee
Bombus impatiens
Common eastern bumble bee
Bombus terrestris
Buff-tailed bumblebee
Linepithema humile
Argentine ant
Megachile rotundata
Alfalfa leafcutting bee
Nasonia vitripennis
Parasitic wasp
Dendroctonus ponderosae
Mountain pine beetle
Tribolium castaneum
Red flour beetle
Rhodnius prolixus
Kissing bug
Orthologs in non-Insect Arthropods (via OrthoDB v9.1) ( EOG090X05CJ )
Organism
Common Name
Gene
Multiple Dmel Genes in this Orthologous Group
Stegodyphus mimosarum
African social velvet spider
Orthologs in non-Arthropod Metazoa (via OrthoDB v9.1) ( None identified )
No non-Arthropod Metazoa orthologies identified
Paralogs
Paralogs (via DIOPT v7.1)
Drosophila melanogaster (Fruit fly) (0)
No records found.
Human Disease Associations
FlyBase Human Disease Model Reports
Disease Model Summary Ribbon
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 1 )
Allele
Disease
Evidence
References
Potential Models Based on Orthology ( 1 )
Human Ortholog
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 0 )
Allele
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease Associations of Human Orthologs (via DIOPT v7.1 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:
Select Layout:
Legend:
Protein
RNA
Selected Interactor(s)
Interactions Browser

Please see the Physical Interaction reports below for full details
protein-protein
Physical Interaction
Assay
References
Summary of Genetic Interactions
esyN Network Diagram
esyN Network Key:
Suppression
Enhancement

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)
Monomer.
(UniProt, P54623 )
Linkouts
BioGRID - A database of protein and genetic interactions.
DroID - A comprehensive database of gene and protein interactions.
InterologFinder - Protein-protein interactions (PPI) from both known and predicted PPI data sets.
MIST (protein-protein) - An integrated Molecular Interaction Database
Pathways
Gene Group - Pathway Membership (FlyBase)
External Data
Linkouts
Genomic Location and Detailed Mapping Data
Chromosome (arm)
2R
Recombination map
2-68
Cytogenetic map
Sequence location
2R:13,439,314..13,450,475 [-]
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
50A8-50A9
Limits computationally determined from genome sequence between P{EP}DpEP358 and P{lacW}drkk13809&P{EP}mip120EP606
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
50A-50A
50A3-50A6
(determined by in situ hybridisation)
Experimentally Determined Recombination Data
Right of (cM)
Notes
Stocks and Reagents
Stocks (19)
Genomic Clones (27)
cDNA Clones (73)
 

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 GBrowse for alignment of the cDNAs and ESTs to the gene model.

cDNA clones, fully sequences
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
    GenomeRNAi - A database for cell-based and in vivo RNAi phenotypes and reagents
    Antibody Information
    Laboratory Generated Antibodies
    Commercially Available Antibodies
     
    Other Information
    Relationship to Other Genes
    Source for database identify of
    Source for database merge of
    Source for merge of: cnn oblivious
    Source for merge of: cnn mat(2)syn-C
    Source for merge of: cnn CG18370
    Additional comments
    Source for merge of cnn CG18370 was sequence comparison ( date:001104 ).
    Other Comments
    cnn is required for efficient recruitment of pericentriolar material.
    Gene expression is increased in response to the presence of either one or two copies of Scer\GAL4hs.PB.
    RNAi screen using dsRNA made from templates generated with primers directed against this gene causes decreased γ-tubulin staining at the spindle pole when assayed in S2 cells. This phenotype can be observed when the screen is performed with or without Cdc27 dsRNA.
    SL2 cells treated with dsRNA against cnn do not show a significant difference in the mitotic index compared to control cells. The treated cells show anastral bipolar spindle arrangements, with anastral poles that are often barrel-shaped and unfocused, however in spite of these abnormalities, anaphase progresses normally in these cells without and increase in abnormal chromosome arrangement compared to control cells.
    dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
    cnn is required for the assembly and function of centrosomes during the syncytial cleavage divisions in the embryo.
    Transcription start sites of cnn and cbs are separated by a mere 134bp. Overall orientation not stated: cnn- cbs+
    cnn is an essential core component of early embryonic centrosomes.
    cnn is required for spindle organisation during male meiosis and for organisation of the sperm axoneme.
    Maternal effect mutations at the cnn locus prevent the correct restructuring of cortical microfilaments in the early embryo.
    cnn function is required for synchronous nuclear divisions in the early embryo, and for various morphological processes in the female and male germlines.
    Protein product associated with centrosomes during blastoderm cell cycles and then with centrosomes of mitotic cells.
    cnn exists as a monomer in the cytoplasm and is phosphorylated.
    cnn is an essential component of the centrosome, it is localised to the centrosome independent of microtubules. Postblastoderm stage cnn localisation and localisation during spermatogenesis and oogenesis is cell-cycle-dependent.
    Identified by immunopurification as a target gene for Antp. cnn encodes a centrosomal protein, may be involved in the assembly of mitotic spindles and maps to a genomic region required for midgut morphogenesis.
    Identification: cnn was identified in a screen for genomic DNA bound by homeotic proteins.
    Genetic, cell biological and biochemical data suggest that the cnn product controls morphogenesis through mediating microtubule organization and is homeotically regulated.
    Mutation in cnn results in a maternal effect phenotype with defects during syncytial blastoderm formation.
    Origin and Etymology
    Discoverer
    Etymology
    Identification
    External Crossreferences and Linkouts ( 96 )
    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.
    UniProt/Swiss-Prot - Manually annotated and reviewed records of protein sequence and functional information
    UniProt/TrEMBL - Automatically annotated and unreviewed records of protein sequence and functional information
    Other crossreferences
    BDGP expression data - Patterns of gene expression in Drosophila embryogenesis
    Drosophila Genomics Resource Center - Drosophila Genomics Resource Center (DGRC) cDNA clones
    Eukaryotic Promoter Database - A collection of databases of experimentally validated promoters for selected model organisms.
    Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
    Flygut - An atlas of the Drosophila adult midgut
    GenomeRNAi - A database for cell-based and in vivo RNAi phenotypes and reagents
    iBeetle-Base - RNAi phenotypes in the red flour beetle (Tribolium castaneum)
    InterPro - A database of protein families, domains and functional sites
    KEGG Genes - Molecular building blocks of life in the genomic space.
    modMine - A data warehouse for the modENCODE project
    Linkouts
    BioGRID - A database of protein and genetic interactions.
    DroID - A comprehensive database of gene and protein interactions.
    DRSC - Results frm RNAi screens
    FLIGHT - Cell culture data for RNAi and other high-throughput technologies
    FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
    FlyCyc Genes - Genes from a BioCyc PGDB for Dmel
    FlyMine - An integrated database for Drosophila genomics
    Interactive Fly - A cyberspace guide to Drosophila development and metazoan evolution
    InterologFinder - Protein-protein interactions (PPI) from both known and predicted PPI data sets.
    MIST (protein-protein) - An integrated Molecular Interaction Database
    Synonyms and Secondary IDs (17)
    Reported As
    Symbol Synonym
    CG18370
    Cnn
    (Magnaghi-Jaulin et al., 2019, Citron et al., 2018, Ramani et al., 2018, Tillery et al., 2018, Feng et al., 2017, Lattao et al., 2017, Khire et al., 2016, Meghini et al., 2016, Eisman et al., 2015, Homem et al., 2015, Yalgin et al., 2015, Hayward et al., 2014, Sechi et al., 2014, Singh et al., 2014, Zheng et al., 2014, Moutinho-Pereira et al., 2013, Fabian and Brill, 2012, Gopalakrishnan et al., 2012, Guilgur et al., 2012, Reschen et al., 2012, Roque et al., 2012, Cho et al., 2011, Mottier-Pavie et al., 2011, Richter et al., 2011, Sabino et al., 2011, Szafer-Glusman et al., 2011, Van Damme et al., 2011, Fabian et al., 2010, Godin et al., 2010, Bucciarelli et al., 2009, Krahn et al., 2009, Mottier-Pavie and Megraw, 2009, Moutinho-Pereira et al., 2009, Rebollo et al., 2009, Robinett et al., 2009, Sheng et al., 2009, Stevens et al., 2009, Vale et al., 2009, Zhang et al., 2009, Basto et al., 2008, Dobbelaere et al., 2008, Eisman et al., 2008, Goshima et al., 2008, Maurange et al., 2008, Mottier et al., 2008, Pimenta-Marques et al., 2008, Rodrigues-Martins et al., 2008, Rogers et al., 2008, Bonaccorsi et al., 2007, Dix and Raff, 2007, Dix and Raff, 2007, Giansanti et al., 2007, Goshima et al., 2007, Pandey et al., 2007, Peel et al., 2007, Rebollo et al., 2007, Rusan and Peifer, 2007, Varmark et al., 2007, Basto et al., 2006, Bowman et al., 2006, Hutterer et al., 2006, Maiato et al., 2006, Schneider et al., 2006, Slack et al., 2006, Verollet et al., 2006, Siller et al., 2005, Yamashita et al., 2005, Blagden and Glover, 2003, Riggs et al., 2003, Megraw et al., 2001, Li et al., 1998, Li, 1995.9.7, Li et al., 1995)
    cnn
    (Guan et al., 2019, Hughes and Simmonds, 2019, Hughes et al., 2018, Riparbelli et al., 2018, Tovey et al., 2018, Golub et al., 2017, Neuert et al., 2017, Poulton et al., 2017, John et al., 2016, Ramdas Nair et al., 2016, Sanghavi et al., 2016, Zheng et al., 2016, Baumbach et al., 2015, Chen et al., 2015, Conduit et al., 2015, Eisman et al., 2015, Gene Disruption Project members, 2015-, Liu et al., 2015, Rodrigues et al., 2015, Venkei and Yamashita, 2015, Ashwal-Fluss et al., 2014, Conduit et al., 2014, Gallaud et al., 2014, Zaytseva et al., 2014, Eisman and Kaufman, 2013, Jauffred et al., 2013, Yadlapalli and Yamashita, 2013, Yamashita, 2013, Fabian and Brill, 2012, Habermann et al., 2012, Japanese National Institute of Genetics, 2012.5.21, Sanghavi et al., 2012, Tao et al., 2012, Chen et al., 2011, Cheng et al., 2011, Gopalakrishnan et al., 2011, Lerit and Gavis, 2011, Sato et al., 2011, Taniguchi et al., 2011, Taniguchi et al., 2011, Wertheim et al., 2011, Buffin and Gho, 2010, Conduit and Raff, 2010, Conduit et al., 2010, Cunha et al., 2010, Gan et al., 2010, Inaba et al., 2010, Moutinho-Pereira et al., 2010, Müller et al., 2010, Riparbelli and Callaini, 2010, Blachon et al., 2009, Cabernard and Doe, 2009, Eisman et al., 2009, Kao and Megraw, 2009, Meireles et al., 2009, Rahmani et al., 2009, Wainman et al., 2009, Blachon et al., 2008, Castellanos et al., 2008, Doheny et al., 2008, Giansanti et al., 2008, Liu and Lehmann, 2008, Megraw et al., 2008, Siller and Doe, 2008, Somma et al., 2008, Wei et al., 2008, Bakal et al., 2007, Brunk et al., 2007, Brunk et al., 2007, Buffin et al., 2007, Cabernard et al., 2007, Christensen and Cook, 2007.3.22, Christensen and Cook, 2007.3.22, Christensen and Cook, 2007.5.8, Egger et al., 2007, Georlette et al., 2007, Lucas and Raff, 2007, Rickmyre et al., 2007, Riparbelli et al., 2007, Slack et al., 2007, Yamashita et al., 2007, Yamashita et al., 2007, Zhang and Megraw, 2007, Colombie et al., 2006, Eisman et al., 2006, Lee et al., 2006, Mahoney et al., 2006, Muller et al., 2006, Nystul and Spradling, 2006, Riparbelli and Callaini, 2005, Yamashita et al., 2005, Raynaud-Messina et al., 2004)
    mat(2)syn-C
    mfs
    Name Synonyms
    maternal effect syncytial blastoderm arrest C
    Secondary FlyBase IDs
    • FBgn0002675
    • FBgn0020264
    • FBgn0033839
    Datasets (0)
    Study focus (0)
    Experimental Role
    Project
    Project Type
    Title
    References (381)