FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\RhoGAP100FCD
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General Information
Symbol
Dmel\RhoGAP100FCD
Species
D. melanogaster
Name
FlyBase ID
FBal0284969
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
syd-1CD
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Caused by aberration
Cytology
Description

Scer\FRT-mediated recombination between the two progenitor insertions has resulted in deletion of the genomic sequence between them (deletion of 30884bp). This removes RhoGAP100F and most of FeCH.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Comment:

Scer\FRT-mediated recombination between the two progenitor insertions has resulted in deletion of the genomic sequence between them (deletion of 30884bp). This removes RhoGAP100F and most of FeCH.

Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

R7 axon terminals in RhoGAP100Fw46/RhoGAP100FCD animals often fail to contact the M6 layer of the medulla. Some R7 axon terminals project thin extensions beyond M6.

Axon terminals of homozygous R7 photoreceptor cell clones often fail to contact the M6 layer of the medulla. Those axons that do contact M6 have abnormally small terminal boutons which often project thin extensions beyond M6. The mutant axon terminals are indistinguishable from wild type at 24 hours after puparium formation (APF), but at 55 hours APF the defect of R7 axons failing to contact M6 is maximal. The mutant R7 axons do not project extensions at 55 hours APF, but extensions are visible by 72 hours APF.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

Expression of Liprin-αScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4Act.PU in RhoGAP100FCD R7 photoreceptor cell clones partially suppresses the failure of the axon terminals to contact the M6 layer of the medulla. The later tendency for R7 axons that do reach the M6 layer to project extensions is not suppressed.

Expression of Liprin-βScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4Act.PU in RhoGAP100FCD R7 photoreceptor cell clones has no effect on either the failure of the axon terminals to contact the M6 layer of the medulla or the tendency for the R7 axons that do reach the M6 layer to project extensions.

Expression of trioScer\UAS.cBa under the control of Scer\GAL4Act.PU in RhoGAP100FCD R7 photoreceptor cell clones almost completely suppresses the failure of the axon terminals to contact the M6 layer of the medulla. The later tendency for R7 axons that do reach the M6 layer to project extensions is partially suppressed.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of RhoGAP100FScer\UAS.T:Zzzz\FLAG under the control of Scer\GAL4Act.PU rescues the axon terminal defects seen in RhoGAP100FCD R7 photoreceptor cell clones.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (2)