A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Gene Dmel\rod

General Information
SymbolDmel\rodSpeciesD. melanogaster
Namerough dealAnnotation symbolCG1569
Feature typeprotein_coding_geneFlyBase IDFBgn0003268
Created / Updated2003-12-01/2003-12-01
Genomic Location
Chromosome (arm)3RRecombination map3-105.1
Cytogenetic map100C6-100C7Sequence location3R:27,406,394..27,413,861 [+]
Map ( GBrowse ) detailed view
hide Summary Information
Automatically generated summary

See sections below for more information
The gene rough deal is referred to in FlyBase by the symbol rod (CG1569, FBgn0003268). It has the cytological map location 100C6-100C7. Its sequence location is 3R:27406394..27413861. Its molecular function is unknown. It is involved in the biological processes: mitotic cell cycle spindle assembly checkpoint; mitotic sister chromatid segregation. 19 alleles are reported. The phenotypes of these alleles are annotated with: mitotic anaphase; nuclear chromosome; eye; anterior fascicle; spermatocyte; meiotic cell cycle. It has one annotated transcript and one annotated polypeptide.

hide Phenotypic Description from the Red Book (Lindsley & Zimm 1992)
Gene/Allele symbols may differ from current usage
rod: rough deal
Mutants show mitotic abnormalities in larval neuroblasts; there is a high frequency of both aneuploid cells and abnormal anaphase figures, with lagging chromatids, anaphase bridges, and stretched chromatid arms. Abnormal chromosome behavior also occurs in the second meiotic anaphase in male meiosis, although motile sperm are produced. All surviving homozygous females and 90% of surviving homozygous males are sterile and have roughened eyes, sparse abdominal bristles, and notched wings.
hide Detailed Mapping Data
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
100C6-100C7  
Limits computationally determined from genome sequence between P{EP}pygoEP1076 and P{PZ}ttk02667&P{lacW}ttkj6C7  
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
100C5-100C5
100C-100D
(determined by in situ hybridisation)  
Experimentally Determined Recombination Data
Location
3-105.1
 
Left of (cM)
Right of (cM)
Notes
Molecular Map Data
Gene Order (in direction of increasing cytology)
References
In direction of increasing cytology: pygo- rod+
Gene Order (overall orientation not stated)
References
hide Gene Model & Products
Please see the GBrowse view of Dmel\rod for information on other features
detailed view FBtr0085795 FBtr0085806 FBtr0085796 FBpp0085167 FBpp0085156 FBpp0085157 FBti0007905 FBti0059563 FBti0021415 FBti0066677 FBti0039855 FBti0011554 FBti0049642 FBti0014607
Comments on Gene Model
Predicted protein sequences differs from that of Accession Q96695. The difference is likely due to a frame shift mutation in either the reference sequence or the reported sequence Q96695.
hide Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Associated CDS (aa)
FBtr0085795
  6653
  2089
Additional Transcript Data & Comments
Reported size (kB)
Comments
External Data
Crossreferences
hide Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kD)
Length (aa)
Theoretical pI
RefSeq ID
GenBank protein
rod-PA  
FBpp0085156  
239.7  
2089  
6.07  
Additional Polypeptide Data & Comments
Reported size (kD)
2098 (aa); 200 (kD observed); 240 (kD predicted)
Comments
External Data
Linkouts
PANTHER - Protein classification by function, families, and pathways
Crossreferences
hide Sequences Consistent with the Gene Model
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
    UniProtKB/TrEMBL
    Maps to
    Does NOT map to
    Identified with
    hide Mapped Features & Mutations
    Please see GBrowse or insertion reports for information on insertions of transgenic constructs and features not listed here
    Type
    Symbol & Location
    Additional Notes
    References
    deletion
    comment=nucleotides 538-5109 of GB:AF114152 deleted
    evidence=experimental
    deletion
    comment=One of three lesions associated with this mutation; 12 bp deletion.
    evidence=experimental
    deletion
    comment=One of three lesions associated with this mutation; 189 bp deletion.
    evidence=experimental
    hide External Data
    Linkouts
    DEDB - Drosophila exon database: splicing graphs
    Crossreferences
    hide Expression Data
    FlyBase-Curated Data
    Transcript and
    Protein data
    Please see the FlyBase Gene Expression Report for details of gene expression from the literature.
    hide Summary of Transcript Expression
    Stage
    Tissue/Position
    Reference
    Marker for
      Subcellular Localization
      CV Term
      hide Summary of Polypeptide Expression
      Stage
      Tissue/Position
      Reference
       larval stage | third instar
       neuroblast <of> larval brain
       larval stage
       larval brain
       adult stage, spermatogenesis
       spermatocyte
      Marker for
        Subcellular Localization
        CV Term
        hide External Data & Images
        Linkouts
        FLIGHT - Cell culture data for RNAi and other high-throughput technologies
        FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
        GEO (NCBI) - Gene expression data: microarray and other high-throughput technologies
        hide Alleles & Phenotypes
        hide Summary of Allele Phenotypes
        Lethality
        Allele
        Other Phenotypes
        Allele
        Sterility
        Allele
        Phenotype manifest in
        Allele
        nuclear chromosome & mitotic anaphase
        chromatin & mitotic anaphase
        chromatin & mitotic telophase
        hide Classical Alleles ( 15 )
        For All Classical Alleles Show

        Allele of rodClassMutagenStocksKnown lesion
        rod11000 Yes
        rod29D0 Yes
        rodEP34081 --
        rodEY045761 --
        rodH4.80 Yes
        rodRP1530 Yes
        rodX-10 Yes
        rodX-20 --
        rodX-30 --
        rodX-40 --
        rodX-50 Yes
        rodX-60 --
        rodf009671 --
        rodpygo90 Yes
        rodunspecified
          0 --
          hide Alleles Carried on Transgenic Constructs ( 4 )
          For All Alleles Carried on Transgenic Constructs Show

          Allele of rodClassMutagenStocksKnown lesion
          rod+tC3L90 Yes
          rodGD87681 Yes
          rodT:Avic\GFP-EGFP0 Yes
          rodT:Disc\RFP-mRFP0 Yes
          hide Aneuploid Aberrations
          Useful deficiency
          Useful duplication
          Disrupted in
          Not disrupted in
          Duplicated in
          hide Transgenic Constructs & Insertions
          Transgenic Constructs
          Type of construct
          Name
          Expression data
          UAS construct
          characterization construct
          Insertions
          Type of insertions
          Name
          Expression data
          miscellaneous insertions
          insertion of mobile activating element
          hide Related Comments
          Please look at the allele reports for the complete phenotype data
          Mutations in rod result in mitotic segregational failure due to delayed or incomplete release of sister chromatids.
          hide Gene Ontology: Function, Process & Cellular Component ( 7 )
          hide Molecular Function
          CV term
          References
          hide Biological Process
          CV term
          References
          non-traceable author statement
          traceable author statement
          inferred from mutant phenotype
          hide Cellular Component
          CV term
          References
          inferred from direct assay
          inferred from direct assay
          inferred from direct assay
          inferred from direct assay
          inferred from direct assay
          inferred from direct assay
          inferred from direct assay
          inferred from direct assay
          inferred from direct assay
          non-traceable author statement
          inferred from direct assay
          non-traceable author statement
          inferred from direct assay
          hide Sequence Ontology: Class of Gene
          hide Interactions & Pathways
          hide Summary of Genetic Interactions
          Interacts with
          Please look at the allele data for full details of the genetic interactions
          rod allele
          Gene
          References
          unspecified
          hide External Data
          Linkouts
          BioGRID - Interaction data, including yeast 2-hybrid and genetic interactions
          hide Orthologs
          Genome-wide drosophilid orthologs
          Curated drosophilid orthologs
          Linkouts
          InParanoid orthologs - Eukaryotic orthologs
          hide Functional Complementation between Species
          hide Inter-Species Misexpression Data
          Produces phenotype in
          Produces NO phenotype in
          hide Stocks & Reagents
          hide Stocks Listed in FlyBase ( 4 )
          Szeged
          Harvard
          VDRC
          Bloomington
          hide Genomic Clones ( 2 )
          hide cDNA Clones ( 11 )
          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 Sequenced
          BDGP DGC clones
          Other clones
          cDNA Clones, End Sequenced (ESTs)
          BDGP DGC clones
          Other clones
          hide RNAi & Array Information
          Affy Oligo
          Linkouts
          DRSC - RNAi screening (Harvard): high-throughput cell culture data and design
          GenomeRNAi - RNAi phenotypes (Heidelberg): high-throughput cell culture data
          hide Antibody Information
          hide Other Information
          hide Discoverer
          hide Etymology
          hide Identification
          hide Position Effect Variegation Data
          hide Relationship to Other Genes
          Source for database identity of
          Source for identity of: rod CG1569
          Source for database merge of
          Source for merge of: rod EP3408 Source for merge of rod EP3408 was that EP3408 insertion is within rod (and in the right orientation) (date:040519).
          Additional comments
          FlyBase curator comment: "EP3408" overexpression phenotype stated to be due to its effect on pygo but orientation of the P{EP} element suggests otherwise.
          hide Comments About Role
          hide Comments About Molecular Function
          hide Other Comments
          dsRNA has been synthesised against this gene and transfected into 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.
          hide External Crossreferences & Linkouts
          Sequence Crossreferences
          RefSeq (Transcripts)
          RefSeq (Proteins)
          Other Crossreferences
          Linkouts
          BioGRID - Interaction data, including yeast 2-hybrid and genetic interactions
          DEDB - Drosophila exon database: splicing graphs
          DRSC - RNAi screening (Harvard): high-throughput cell culture data and design
          FLIGHT - Cell culture data for RNAi and other high-throughput technologies
          FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
          FlyMine - Integrated genomics database for Drosophila, Anopheles, and C.elegans
          GEO (NCBI) - Gene expression data: microarray and other high-throughput technologies
          GenomeRNAi - RNAi phenotypes (Heidelberg): high-throughput cell culture data
          InParanoid orthologs - Eukaryotic orthologs
          PANTHER - Protein classification by function, families, and pathways
          hide Synonyms & Secondary IDs ( 8 )
          Reported As
          Symbol Synonym
          Name Synonym
          Secondary FlyBase IDs
          • FBgn0044458
          hide References ( 63 )
          Generate a list of
          List References by type