FB2024_03 , released June 25, 2024
Allele: Dmel\clnSF3-2
Open Close
General Information
Symbol
Dmel\clnSF3-2
Species
D. melanogaster
Name
FlyBase ID
FBal0105039
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Cytology
Description
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
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

Homozygotes have extremely rough eyes showing a characteristic "white and red" appearance due to a loss of pigments. The normal structure of the ommatidia is disrupted almost completely. The number of secondary and tertiary pigment cells is increased. Cone cells are deformed and their number and arrangement in the ommatidia is irregular. Homozygotes have normal wing vein patterns, and appear morphologically normal apart from the eye defects. Posterior to the morphogenetic furrow in the eye imaginal disc, relatively normal five-cell ommatidial preclusters form in homozygotes. However, the adjacent region lacks photoreceptor cells. At the posterior region of the eye, clusters with variable numbers of photoreceptor cells are seen. The photoreceptor cells degenerate during pupal development.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhancer of
Statement
Reference

cln[+]/clnSF3-2 is an enhancer of visible | dominant phenotype of rlSu23

cln[+]/clnSF3-2 is an enhancer of visible phenotype of Dsor1Su1, SosJC2

Suppressor of
Statement
Reference

clnSF3-2 is a suppressor of visible phenotype of rprGMR.PW

clnSF3-2 is a suppressor of visible phenotype of Ras85DN17.sev

clnSF3-2 is a suppressor of visible phenotype of aoshs.PSa

Other
Statement
Reference
Phenotype Manifest In
Enhancer of
Statement
Reference

cln[+]/clnSF3-2 is an enhancer of wing phenotype of rlSu23

cln[+]/clnSF3-2 is an enhancer of wing vein | ectopic phenotype of rlSu23

cln[+]/clnSF3-2 is an enhancer of wing vein | ectopic phenotype of Dsor1Su1, SosJC2

cln[+]/clnSF3-2 is an enhancer of wing phenotype of Dsor1Su1, SosJC2

NOT Enhancer of
Statement
Reference

clnSF3-2 is a non-enhancer of phenotype of Ras85DV12.sev

Suppressor of
Statement
Reference

clnSF3-2 is a suppressor of eye phenotype of aoshs.PSa

clnSF3-2 is a suppressor of wing phenotype of aoshs.PSa

clnSF3-2 is a suppressor of eye phenotype of rprGMR.PW

clnSF3-2 is a suppressor of eye phenotype of Scer\GAL4hs.2sev, aosUAS.cTa

clnSF3-2 is a suppressor of eye phenotype of Ras85DN17.sev

clnSF3-2 is a suppressor of ommatidium phenotype of Ras85DN17.sev

cln[+]/clnSF3-2 is a suppressor of phenotype of aosGMR.PS

NOT Suppressor of
Statement
Reference

clnSF3-2 is a non-suppressor of phenotype of Ras85DV12.sev

Other
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

Dominantly suppresses the argosGMR.PS eye phenotype. Has little or no effect on the Ras85DV12.sev eye phenotype. Suppresses the Ras85DN17.sev eye phenotype. Suppresses the argoshs.PSa eye and wing phenotypes. Suppresses the rprGMR.PW cell death and small eye phenotypes. Suppresses the WGMR.PG cell death phenotype. Suppresses the rprGMR.PW cell death and small eye phenotypes. Suppresses the rough eye phenotype caused by expression of argosScer\UAS.cTa under the control of Scer\GAL4hs.2sev. Dsor1Su1/Y ; SosJC2/+ flies have extra wing veins. This phenotype is enhanced by one copy of clnSF3-2. Dominantly enhances the extra wing vein phenotype of rlSu23/+ flies.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer

Selected as: a dominant modifier of the rough eye phenotype caused by argosGMR.PS.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
clnSF3-2
Name Synonyms
Secondary FlyBase IDs
    References (1)