FB2026_03 , released September 17, 2026
Gene: Dmel\bam
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General Information
Symbol
Dmel\bam
Species
D. melanogaster
Name
bag of marbles
Annotation Symbol
CG10422
Feature Type
FlyBase ID
FBgn0000158
Gene Model Status
Stock Availability
Gene Summary
bag of marbles (bam) encodes a protein involved in gametogenesis that is associated with the fusome, a germ cell-specific organelle. It contributes to the fate determination of germline stem cells, in which bam is negatively regulated by the BMP signaling pathway. [Date last reviewed: 2019-03-07] (FlyBase Gene Snapshot)
Also Known As

BamC, Bam-C

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
3-87
RefSeq locus
NT_033777 REGION:25243039..25245109
Sequence
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
Gene Ontology (GO) Annotations (25 terms)
Molecular Function (3 terms)
Terms Based on Experimental Evidence (3 terms)
CV Term
Evidence
References
inferred from direct assay
inferred from direct assay
Terms Based on Predictions or Assertions (0 terms)
Biological Process (19 terms)
Terms Based on Experimental Evidence (19 terms)
CV Term
Evidence
References
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
involved_in gamete generation
inferred from mutant phenotype
inferred from mutant phenotype
inferred from genetic interaction with FLYBASE:mael; FB:FBgn0016034
inferred from direct assay
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
involved_in oogenesis
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
involved_in spermatogenesis
inferred from mutant phenotype
inferred from mutant phenotype
Terms Based on Predictions or Assertions (0 terms)
Cellular Component (3 terms)
Terms Based on Experimental Evidence (3 terms)
CV Term
Evidence
References
located_in fusome
inferred from direct assay
located_in spectrosome
inferred from direct assay
Terms Based on Predictions or Assertions (1 term)
CV Term
Evidence
References
located_in cytoplasm
inferred from experiment
Gene Group / Complex (FlyBase)
Protein Family (UniProt)
-
Summaries
Gene Snapshot
bag of marbles (bam) encodes a protein involved in gametogenesis that is associated with the fusome, a germ cell-specific organelle. It contributes to the fate determination of germline stem cells, in which bam is negatively regulated by the BMP signaling pathway. [Date last reviewed: 2019-03-07]
Pathway (FlyBase)
POSITIVE REGULATORS OF HEDGEHOG SIGNALING PATHWAY -
Positive regulators of hedgehog signaling up-regulate the pathway, resulting in the activation of transcription of hh-responsive genes.
NEGATIVE REGULATORS OF IMD SIGNALING PATHWAY -
Negative regulators of the immune deficiency (Imd) pathway result in the decreased activity of the NFκB-like transcription factor Rel in the nucleus. Negative regulators are important in preventing damage to the host from over-activation of the pathway; preventing inappropriate triggering or terminating the response. (Adapted from FBrf0224587 and FBrf0238555.)
Protein Function (UniProtKB)
Regulatory component of a deubiquitinase complex consisting of bam and otu (PubMed:28484036). The complex deubiquitinates K63-linked polyubiquitinated proteins, antagonizing the ubiquitination activity of Traf6 and regulating the IMD immune signaling pathway (PubMed:30879902). Otu-bam deubiquitinase activity is regulated by Traf6 dependent immune signaling regulation of bam expression levels; this forms a feedback loop that regulates the IMD immune signaling pathway and balances gut immune activity during aging (PubMed:30879902). The complex deubiquitinates and stabilizes CycA/cyclin-A to regulate CycA-dependent differentiation (PubMed:28484036). Required to initiate both male and female gametogenesis (PubMed:2279698). Part of a complex with bgcn involved in 3'-UTR-dependent translational repression of a subset of mRNAs, including those for mei-P26, nanos and shg/E-cadherin (PubMed:19470484, PubMed:19556547, PubMed:23122292). Repression of mei-P26 is targeted by let-7 miRNA (PubMed:23122292). Involved in a regulatory cascade with mei-P26 to control the progression of cystocytes through transit amplification and the switch to spermatocyte differentiation; mei-P26 facilitates bam accumulation, which in turn represses translation of mei-P26 (PubMed:19470484, PubMed:20018708, PubMed:2279698, PubMed:23122292, PubMed:28484036, PubMed:9334284). Forms a complex with tut and bgcn involved in 3'-UTR-dependent post-transcriptional repression of several 3'-RNA processing factors, which promotes germline stem cell lineage differentiation and mitosis-to-meiosis transition (PubMed:25412508, PubMed:28190776).
(UniProt, P22745)
Summary (Interactive Fly)

novel protein involved in oogenesis and spermatogenesis - functions as a translational repressor by interfering with translation initiation - controls the size and organization of the Drosophila hematopoietic niche through interactions with the Insulin-like growth factor pathway and Retinoblastoma-family protein - activates H3K36 trimethylation-mediated epigenetic regulation

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

Please see the JBrowse view of Dmel\bam 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 P22745)

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
PDB - An information portal to biological macromolecular structures
Comments on Gene Model

Gene model reviewed during 5.45

Gene model reviewed during 5.49

Gene model reviewed during 6.24

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0084869
1946
442
Additional Transcript Data and Comments
Reported size (kB)

2.0 (northern blot)

Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
UniProt
RefSeq ID
GenBank
FBpp0084243
50.3
442
6.65
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)

442 (aa); 49 (kD)

Comments
External Data
Subunit Structure (UniProtKB)

Interacts (via central region) with ubiquitin (PubMed:28484036). Interacts (via C-terminus) with otu (via OTU domain); the interaction enhances otu aggregation into amyloid-like structures and enhances its deubiquitinase activity (PubMed:28484036, PubMed:30879902). Together with otu interacts with CycA/cyclin-A (via C-terminus); the interaction stabilizes CycA by promoting and enhancing otu dependent deubiquitination of CycA (PubMed:28484036). Together with otu interacts with Traf6 (PubMed:30879902). Part of a complex composed of at least tut, bam and bgcn; complex formation does not require RNA (PubMed:25412508). Interacts (via C-terminus) with bgcn; the interaction is direct and is not disrupted by eIF4A (PubMed:19470484, PubMed:19556547, PubMed:23122292, PubMed:23526974, PubMed:25412508). Interacts with eIF4A (via multiple contacts); the interaction is direct and is not disrupted by bgcn (PubMed:19556547). Interacts (via N-terminus) with tut; the interaction is direct and mediates the interaction between tut and bgcn (PubMed:25412508). As part of the bam-bgcn-tut complex associates with twin; may recruit the CCR4-NOT1 deadenylation complex to mRNA 3'-UTRs to mediate post-transcriptional regulation of expression (PubMed:28190776). Part of a complex composed of at least mei-P26, bam, bgcn and Sxl; this complex is involved in translational repression of nanos mRNA (PubMed:23526974).

(UniProt, P22745)
Post Translational Modification

Ubiquitinated (C-terminal region).

(UniProt, P22745)
Domain

May possess a C-terminal PEST sequence (rich in Pro, Glu, Ser and Thr) targeting it for degradation and rapid protein turnover.

(UniProt, P22745)
Crossreferences
InterPro - A database of protein families, domains and functional sites
PDB - An information portal to biological macromolecular structures
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\bam 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).

-0.21

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

Comment: not expressed at apical tip of testis

northern blot
Stage
Tissue/Position (including subcellular localization)
Reference
RT-PCR
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data

bam transcript is expresed in two waves: the first in spermatogonia, and the second in early spermatocytes. bam transcript, but not protein, is detected in primary spermatocytes, suggesting that bam protein translation is downregulated.

bam transcripts are expressed throughout oogenesis and in 0-2hr embryos but are absent by 4hr of development. They are also detected in dissected ovaries and testes. In ovaries, bam transcripts are expressed in cystoblasts and/or very early cystocytes. Later they are detected in stage 10 nurse cells, are transferred to the oocyte at the time of nurse cell breakdown, and persist in the mature egg and the early embryo..

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

bam protein is detected in secondary spermatogonial cells at the 4-16 cell stages, with peak expression at the 8 cell stage. bam protein is not detected in spermatocytes.

Marker for
Subcellular Localization
CV Term
Evidence
References
located_in fusome
inferred from direct assay
located_in spectrosome
inferred from direct assay
Expression Deduced from Reporters
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\bam in JBrowse
RNA-Seq by Region - Search RNA-Seq expression levels by exon or genomic region
Reference
See Gelbart and Emmert, 2013 for analysis details and data files for all genes.
Developmental Proteome: Life Cycle
Developmental Proteome: Embryogenesis
External Data and Images
Linkouts
DRscDB - A single-cell RNA-seq resource for data mining and data comparison across species
EMBL-EBI Single Cell Expression Atlas - Single cell expression across species
FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
FlyAtlas2 - A Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data
Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
Flygut - An atlas of the Drosophila adult midgut
Images
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 21 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 68 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of bam
Transgenic constructs containing regulatory region of bam
Aberrations (Deficiencies and Duplications) ( 6 )
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
germarium & germ cell
Orthologs
Human Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Homo sapiens (Human) (0)
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Rattus norvegicus (Norway rat) (0)
Mus musculus (laboratory mouse) (0)
Xenopus tropicalis (Western clawed frog) (0)
Danio rerio (Zebrafish) (0)
Caenorhabditis elegans (Nematode, roundworm) (0)
Anopheles gambiae (African malaria mosquito) (0)
Arabidopsis thaliana (thale-cress) (0)
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:bam. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Human Disease Associations
FlyBase Human Disease Model Reports
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 1 )
Allele
Disease
Evidence
References
Potential Models Based on Orthology ( 0 )
Human Ortholog
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 1 )
Allele
Disease
Interaction
References
model of  germ cell cancer
is ameliorated by Atg173F5
is ameliorated by Atg61
is ameliorated by Cdk23
is ameliorated by InR339
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.
Homo sapiens (Human)
Gene name
Score
OMIM
OMIM Phenotype
DO term
Complementation?
Transgene?
Functional Complementation Data
Functional complementation data is computed by FlyBase using a combination of the orthology data obtained from DIOPT and OrthoDB and the allele-level genetic interaction data curated from the literature.
Interactions
Summary of Physical Interactions
Interaction Browsers

Please see the Physical Interaction reports below for full details
RNA-protein
Physical Interaction
Assay
References
RNA-RNA
Physical Interaction
Assay
References
protein-protein
Physical Interaction
Assay
References
Summary of Genetic Interactions
Interaction Browsers

Please look at the allele data for full details of the genetic interactions
Starting gene(s)
Interaction type
Interacting gene(s)
Reference
Starting gene(s)
Interaction type
Interacting gene(s)
Reference
External Data
Subunit Structure (UniProtKB)
Interacts (via central region) with ubiquitin (PubMed:28484036). Interacts (via C-terminus) with otu (via OTU domain); the interaction enhances otu aggregation into amyloid-like structures and enhances its deubiquitinase activity (PubMed:28484036, PubMed:30879902). Together with otu interacts with CycA/cyclin-A (via C-terminus); the interaction stabilizes CycA by promoting and enhancing otu dependent deubiquitination of CycA (PubMed:28484036). Together with otu interacts with Traf6 (PubMed:30879902). Part of a complex composed of at least tut, bam and bgcn; complex formation does not require RNA (PubMed:25412508). Interacts (via C-terminus) with bgcn; the interaction is direct and is not disrupted by eIF4A (PubMed:19470484, PubMed:19556547, PubMed:23122292, PubMed:23526974, PubMed:25412508). Interacts with eIF4A (via multiple contacts); the interaction is direct and is not disrupted by bgcn (PubMed:19556547). Interacts (via N-terminus) with tut; the interaction is direct and mediates the interaction between tut and bgcn (PubMed:25412508). As part of the bam-bgcn-tut complex associates with twin; may recruit the CCR4-NOT1 deadenylation complex to mRNA 3'-UTRs to mediate post-transcriptional regulation of expression (PubMed:28190776). Part of a complex composed of at least mei-P26, bam, bgcn and Sxl; this complex is involved in translational repression of nanos mRNA (PubMed:23526974).
(UniProt, P22745 )
Linkouts
BioGRID - A database of protein and genetic interactions.
DroID - A comprehensive database of gene and protein interactions.
MIST (genetic) - An integrated Molecular Interaction Database
MIST (protein-protein) - An integrated Molecular Interaction Database
Pathways
Signaling Pathways (FlyBase)
Metabolic Pathways
FlyBase
External Links
External Data
Linkouts
Class of Gene
Genomic Location and Detailed Mapping Data
Chromosome (arm)
3R
Recombination map
3-87
Cytogenetic map
Sequence location
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
96C7-96C8
Limits computationally determined from genome sequence between P{lacW}OstStt3j2D9 and P{PZ}Aats-gln05461
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
96C1-96C9
(determined by in situ hybridisation)
96C-96C
(determined by in situ hybridisation)
Experimentally Determined Recombination Data
Location
Left of (cM)
Right of (cM)
Notes
Stocks and Reagents
Stocks (18)
Genomic Clones (10)
 

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

cDNA Clones (15)
 

Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.

cDNA clones, fully sequenced
BDGP DGC clones
Other clones
Drosophila Genomics Resource Center cDNA clones

For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.

cDNA Clones, End Sequenced (ESTs)
BDGP DGC clones
    RNAi and Array Information
    Linkouts
    DRSC - Results frm RNAi screens
    Antibody Information
    Laboratory Generated Antibodies
     

    polyclonal

    monoclonal

    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

      bam is epistatic to somatic niche piwi function in the ovary, but germline piwi is epistatic to bam function in the ovary.

      Forced premature expression of bam in early male germ cells (stem cells, gonialblasts and spermatogonia) leads to accumulation of male germ cells at the single-cell stage and then death of the early male germ cells.

      The down-regulation of bam protein is essential for the initiation of cystocyte differentiation into functional egg chambers.

      bam and bgcn cooperatively regulate cystoblast differentiation by controlling localization of bam protein to the fusome.

      bgcn is essential for the localization of bam protein to the fusome.

      In a sample of 79 genes with multiple introns, 33 showed significant heterogeneity in G+C content among introns of the same gene and significant positive correspondence between the intron and the third codon position G+C content within genes. These results are consistent with selection adding against preferred codons at the start of genes.

      Mosaic analysis demonstrates bam and bgcn act autonomously in the germline to restrict germ cell proliferation during spermatogenesis. Results suggest bam and bgcn regulate progression through the male germline stem cell lineage by cell-intrinsically restricting the proliferation of amplifying germ cells. bgcn function is not required for the proper expression of bam protein.

      Germ cells accumulating in bam or bgcn mutants testis most resemble amplifying germ cells, because they undergo incomplete cytokinesis and progress through the cell cycle in synchrony within a cyst.

      Disruption of bam expression in enc mutant ovaries suggests enc has a role early in cyst development.

      enc is a negative regulator of bam.

      Mutations in bam disrupt cyst formation producing tumorous egg chambers.

      Phenotypic analysis of bam-;hts- ovaries shows bam is epistatic to hts.

      Anti-bam antibodies can recognise bam in two distinct cellular compartments, the fusome and the cytoplasm.

      bam is required to promote incomplete cytokinesis and activate fusome growth.

      Mutants display germline hyperplastic phenotype.

      Partial germline sex transformation occurs in otu, snf, Sxl and bam ovarian tumors.

      bam is involved in the initiation of gametogenesis.

      reference: Spradling and McKearin, personal communication.

      bam is essential for male and female fertility but not for viability.

      Relationship to Other Genes
      Source for database merge of
      Additional comments
      Nomenclature History
      Source for database identify of
      Nomenclature comments
      Etymology

      Named "bag of marbles" for cyst-like clusters of undifferentiated germ cells in mutant testes and ovaries resembling a bag of marbles.

      Synonyms and Secondary IDs (18)
      Reported As
      Symbol Synonym
      Bam
      (Fang et al., 2026, Fu et al., 2026, Liu et al., 2026, Noh et al., 2025, Clémot et al., 2024, Fu et al., 2024, Finger et al., 2023, Zhang et al., 2023, Diegmiller et al., 2022, Montanari et al., 2022, Szarka-Kovács et al., 2022, Reilein et al., 2021, Sou et al., 2021, Vidaurre and Chen, 2021, Blatt et al., 2020, Kelleher et al., 2020, Luo et al., 2020, Malik et al., 2020, Rust et al., 2020, Angulo et al., 2019, Malik et al., 2019, Clémot et al., 2018, Carbonell et al., 2017, Malik et al., 2017, Moschall et al., 2017, Upadhyay et al., 2017, Wu et al., 2016, Yadav et al., 2016, Yu et al., 2016, Dolezal et al., 2015, Dorn and Dorn, 2015, Greenspan et al., 2015, Tokusumi et al., 2015, Clough et al., 2014, Hamada-Kawaguchi et al., 2014, Pargett et al., 2014, Shields et al., 2014, Vartiainen et al., 2014, Zhang et al., 2014, Bausek, 2013, Chen et al., 2013, Davies et al., 2013, Li et al., 2013, Stine and Matunis, 2013, Zhang et al., 2013, Lim et al., 2012, Matunis et al., 2012, Siddiqui et al., 2012, White-Cooper, 2012, Eliazer and Buszczak, 2011, Harris and Ashe, 2011, Issigonis and Matunis, 2011, König et al., 2011, Ali et al., 2010, Kim et al., 2010, Leatherman and Dinardo, 2010, Yamashita et al., 2010, Hayashi et al., 2009, Sheng et al., 2009, Kim et al., 2008, Leatherman and DiNardo, 2008, Maines et al., 2008, Sheng et al., 2008, Bogard et al., 2007, Flores et al., 2007, Hime et al., 2007, Li et al., 2007, Shcherbata et al., 2007, Sheng et al., 2007, Chen and McKearin, 2003, Kiger et al., 2000)
      bam
      (Bener et al., 2026, Bener et al., 2026, Matsui et al., 2026, Zhang et al., 2026, Arnce et al., 2025, Arnce et al., 2025, Bener et al., 2025, Gordon et al., 2025, Harris et al., 2025, Kagemann et al., 2025, Mercer et al., 2025, Samuels et al., 2025, Sutcliffe et al., 2025, Xu et al., 2025, Eslahi et al., 2024, Huang et al., 2024, Jansen et al., 2024, Miao et al., 2024, Ridwan et al., 2024, Rojas-Ríos et al., 2024, Anderson et al., 2023, Breznak et al., 2023, Butsch et al., 2023, Cabrita and Martinho, 2023, Gui et al., 2023, Gupta et al., 2023, Jang and Kim, 2023, Liu et al., 2023, Pang et al., 2023, Shen et al., 2023, Sperling and Glover, 2023, Wenzel and Aquadro, 2023, Wenzel and Aquadro, 2023, Yildirim et al., 2023, Zhang et al., 2023, Berry et al., 2022, Bubnell et al., 2022, Chen et al., 2022, Ilyin et al., 2022, Kitzman et al., 2022, Lim et al., 2022, Martin et al., 2022, McCarthy et al., 2022, Pavlidaki et al., 2022, Shapiro-Kulnane et al., 2022, Varga et al., 2022, Wang et al., 2022, Zhao et al., 2022, Zinshteyn and Barbash, 2022, Banisch et al., 2021, Blatt et al., 2021, Bubnell et al., 2021, Casale et al., 2021, Chaouch et al., 2021, Chen et al., 2021, Climent-Cantó et al., 2021, Connacher and Goldstrohm, 2021, Finger et al., 2021, Gong et al., 2021, Hoshino and Niwa, 2021, Kahney et al., 2021, Koreman et al., 2021, Malik, 2021, Morin-Poulard et al., 2021, Nandi and Chowdhuri, 2021, Slaidina et al., 2021, Tao et al., 2021, Witt et al., 2021, Yang, 2021, Yuen et al., 2021, Yu et al., 2021, Ågren et al., 2020, Carvalho-Santos et al., 2020, DeLuca et al., 2020, Hinnant et al., 2020, Ote and Yamamoto, 2020, Rastegari et al., 2020, Shi et al., 2020, Zhang and Cai, 2020, Bhattacharjee et al., 2019, Chen et al., 2019, Drummond-Barbosa, 2019, Gao et al., 2019, Hudry et al., 2019, Ji et al., 2019, Lieber et al., 2019, Li et al., 2019, Luhur et al., 2019, Maksimov and Koryakov, 2019, Nelson et al., 2019, Primus et al., 2019, Story et al., 2019, Tiwari et al., 2019, Witt et al., 2019, Wooten et al., 2019, Yoshinari et al., 2019, Chen et al., 2018, Flora et al., 2018, Gene Disruption Project members, 2018-, Hao et al., 2018, Jain et al., 2018, Kang et al., 2018, Laktionov et al., 2018, Maksimov et al., 2018, McCarthy et al., 2018, Mehrotra and Deshpande, 2018, Osman and Pek, 2018, Tokusumi et al., 2018, Tseng et al., 2018, Zhao et al., 2018, Cheng et al., 2017, Feng et al., 2017, Ji et al., 2017, Kim et al., 2017, Ma et al., 2017, Misra et al., 2017, Monsivais et al., 2017, Salz et al., 2017, Shan et al., 2017, Yang et al., 2017, Bowman and Tatar, 2016, Carreira-Rosario et al., 2016, Cruz-Becerra et al., 2016, Li et al., 2016, Ma et al., 2016, Sanchez et al., 2016, Sarov et al., 2016, Yu et al., 2016, Dolezal et al., 2015, Eikenes et al., 2015, Flores et al., 2015, Fu et al., 2015, Kao et al., 2015, Lengil et al., 2015, Lim et al., 2015, Liu et al., 2015, Luo et al., 2015, Shapiro-Kulnane et al., 2015, Sieber and Spradling, 2015, Singh, 2015, Sun et al., 2015, Teixeira et al., 2015, Xing and Li, 2015, Yu et al., 2015, Chen et al., 2014, Eliazer et al., 2014, Evans et al., 2014, Herzig et al., 2014, Kuuluvainen et al., 2014, Ma et al., 2014, Maimon et al., 2014, Matsuoka et al., 2014, Pan et al., 2014, Toshima et al., 2014, Tseng et al., 2014, Wylie et al., 2014, Xue et al., 2014, Yan et al., 2014, Barton et al., 2013, Chang et al., 2013, Eikenes et al., 2013, Eun et al., 2013, Hernández et al., 2013, Jin et al., 2013, Joly et al., 2013, Li et al., 2013, Mathieu et al., 2013, Xin et al., 2013, Zhao et al., 2013, Bunt et al., 2012, Cash and Andrews, 2012, Chau et al., 2012, Insco et al., 2012, Japanese National Institute of Genetics, 2012.5.21, Li et al., 2012, Lim et al., 2012, Lu et al., 2012, Matunis et al., 2012, Meier et al., 2012, Monk et al., 2012, Tian et al., 2012, White-Cooper, 2012, Xia et al., 2012, Chan et al., 2011, Deng et al., 2011, Eliazer and Buszczak, 2011, Eliazer et al., 2011, Gancz et al., 2011, 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      fs(3)neo61
      Name Synonyms
      Bag-of-Marbles
      bag of marble
      Secondary FlyBase IDs
        Datasets (0)
        Study focus (0)
        Experimental Role
        Project
        Project Type
        Title
        Study result (0)
        Result
        Result Type
        Title
        External Crossreferences and Linkouts ( 134 )
        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.
        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
        UniProt/TrEMBL - Automatically annotated and unreviewed records of protein sequence and functional information
        Other crossreferences
        AlphaFold DB - AlphaFold provides open access to protein structure predictions for the human proteome and other key proteins of interest, to accelerate scientific research.
        DRscDB - A single-cell RNA-seq resource for data mining and data comparison across species
        EMBL-EBI Single Cell Expression Atlas - Single cell expression across species
        FlyAtlas2 - A Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data
        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)
        PDB - An information portal to biological macromolecular structures
        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
        Interactive Fly - A cyberspace guide to Drosophila development and metazoan evolution
        MIST (genetic) - An integrated Molecular Interaction Database
        MIST (protein-protein) - An integrated Molecular Interaction Database
        References (607)