FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\SX155
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General Information
Symbol
Dmel\SX155
Species
D. melanogaster
Name
FlyBase ID
FBal0030194
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Mutagen
Nature of the Allele
Allele class
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

Homozygous mutant clones cause vein-loss phenotypes, sometimes extending a few cells outside the clone boundary. In other cases, vein truncation is rescued within the border of the clone. These reciprocal forms of local cell non-autonomy appear to depend on the shape of the clone, an island of cells tend to take on the vein phenotype associated with the surrounding cells. Homozygous mutant clones on the dorsal side of the wing tend to remove both dorsal and ventral components of the wing vein, however ventral clones generally only affect the ventral components. Homozygous Minute clones reveal that wing veins L1, L2, L3, and L4 are often almost completely eliminated, though for L3, and L4 only the distal halves of the vein are typically affected. The anterior marginal vein L1 is never affected. The overall pattern of vein loss is very similar to rho6 clones, though clones lacking SX155 seem to have slightly stronger vein-loss phenotypes extending more proximally than rho6.

Projection patterns of retinal axons in heterozygous larvae are indistinguishable from wild type.

Clonal analysis of Star alleles shows that the progression of the morphogenetic furrow is delayed and dpp expression was inhibited near the clones.

Homozygous clones in the eye are always associated with a scar, surrounded by normal ommatidia of mixed genotype.

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

SX155 is an enhancer of phenotype of aoshs.PSa

Suppressor of
Statement
Reference

SX155/S[+] is a suppressor of phenotype of aos257

SX155 is a suppressor of retina & axon phenotype of aos257

Additional Comments
Genetic Interactions
Statement
Reference

The addition of SX155 to stetScer\UAS.cGa, Scer\GAL4Bx-MS1096 flies almost completely suppresses the ectopic vein phenotype seen in these flies.

Overexpression of rhoScer\UAS.cBa driven by Scer\GAL4Bx-MS1096 in SX155 homozygous clones, produced a SX155 type phenotype, the rhoScer\UAS.cBa induced solid wing phenotype is completely suppressed.

Suppresses the retinal axon phenotype caused by argos257.

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

Analysis of ommatidia of mixed genotype at the edge of clones in the eye indicates that photoreceptor cells R2, R5 and R8 require the S gene product for normal development, but photoreceptor cells R1, R3, R4, R6 and R7 do not.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (8)