FB2024_03 , released June 25, 2024
Allele: Dmel\dx152
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General Information
Symbol
Dmel\dx152
Species
D. melanogaster
Name
FlyBase ID
FBal0217806
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Imprecise excision of the progenitor insertion, resulting in a 2795bp deletion 3' to the original insertion site.

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

2795 bp deletion resulting from the imprecise excision of P{EP}dxDelta64.

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

One copy of dx152 has no effect on eye size.

dx152 hemizygous adult males (but not heterozygous females) display vein deltas in the wing.

Hemizygotes show distal wing vein thickening with occasional wing notching.

Homozygotes and hemizygotes are viable and fertile. They show wing vein thickening in 100% of cases, and a notch at the wing tip in 5% of cases.

dxENU/dx152 and dx24/dx152 flies show wing vein thickening.

dx1/dx152 flies show wing vein thickening and can show wing notching.

Homozygotes show a mild rotation defect in the ommatidia and some symmetrical R3/R3 ommatidia being seen. Photoreceptor cell number is normal.

Interocellar bristles are disorganised in 70% of homozygotes and fusion of the ocelli is seen in 2% of cases.

Mutants have normal legs, macrochaetae and microchaetae.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement
Reference

dx152 has visible | adult stage | male phenotype, enhanceable by Kap-α3D93

dx152 has visible | adult stage | male phenotype, enhanceable by Kap-α3D165

dx152 has visible | adult stage | male phenotype, enhanceable by Kap-α3S033513

dx152 has visible phenotype, enhanceable by sca[+]/scad09400

dx152 has visible phenotype, enhanceable by klud00059/klu[+]

dx152 has visible phenotype, enhanceable by GPHRc06331/CG8090[+]

dx152 has visible | recessive phenotype, enhanceable by DeltaRevF10/Dl[+]

Suppressed by
Statement
Reference

dx152 has visible phenotype, suppressible by f06222f06222/f06222[+]

dx152 has visible | recessive phenotype, suppressible by Su(H)[+]/Su(H)del47

dx152 has visible | recessive phenotype, suppressible by Su(H)[+]/Su(H)T4

Suppressor of
Statement
Reference

dx152/dx[+] is a suppressor | partially of visible phenotype of Scer\GAL4ey.PU, maheUAS.Tag:HA

dx152/dx[+] is a suppressor of visible | dominant phenotype of NAx-E2

Other
Statement
Reference
Phenotype Manifest In
Enhanced by
Statement
Reference

dx152 has wing vein | male phenotype, enhanceable by Kap-α3D93

dx152 has wing vein | male phenotype, enhanceable by Kap-α3D165

dx152 has wing vein | male phenotype, enhanceable by Kap-α3S033513

dx152 has wing vein phenotype, enhanceable by sca[+]/scad09400

dx152 has wing vein phenotype, enhanceable by klud00059/klu[+]

dx152 has wing phenotype, enhanceable by klud00059/klu[+]

dx152 has wing vein phenotype, enhanceable by GPHRc06331/CG8090[+]

dx152 has wing phenotype, enhanceable by Su(H)[+]/Su(H)T4

dx152 has wing vein phenotype, enhanceable by DeltaRevF10/Dl[+]

dx152 has ocellus phenotype, enhanceable by DeltaRevF10/Dl[+]

Suppressed by
Statement
Reference

dx152 has wing vein phenotype, suppressible by f06222f06222/f06222[+]

dx152 has wing vein phenotype, suppressible by Su(H)[+]/Su(H)del47

Suppressor of
Statement
Reference

dx152/dx[+] is a suppressor | partially of eye phenotype of Scer\GAL4ey.PU, maheUAS.Tag:HA

dx152/dx[+] is a suppressor of wing vein L5 | distal phenotype of NAx-E2

Other
Additional Comments
Genetic Interactions
Statement
Reference

One copy of dx152 marginally suppresses the reduced eye phenotype seen when maheScer\UAS.T:Ivir\HA1 is expressed under the control of Scer\GAL4ey.PU in 32% of eyes examined.

The wing vein deltas and extra vein material observed in dx152 hemizygous adult males is exacerbated by combination with single copy of any of the following alleles: Kap-α3D93, Kap-α3D165 or Kap-α3S033513. No wing defects are observed in adult females double heterozygote for dx152 and any of the aforementioned Kap-α3 alleles.

The wing vein defects of dx152 hemizygotes are enhanced by one copy of scad09400, klud00059 or CG8090c06331. For klud00059 the degree and penetrance of wing notching is also more severe.

f06222f06222 completely suppresses the dx152 wing vein defects.

The mild wing vein thickening phenotype seen in Df(1)N-54l9/+ flies is enhanced if they are also carrying dx152/+.

dx152/+ completely suppresses the loss of the distal end of wing vein L5 which is seen in NAx-E2/+ flies.

DlRevF10/+ enhances the wing vein thickening phenotype of dx152 hemizygotes. The second and third tarsal segments of the forelegs are fused in 41% of the double mutants, a phenotype that is not seen in either dx152 hemizygotes or DlRevF10/+ animals. The double mutants show fusion of the ocelli in 37% of cases, compared to the 2% penetrance seen in dx152 hemizygotes.

Su(H)del47/+ suppresses the wing vein thickening seen in dx152 hemizygotes.

Su(H)T4/+ enhances the wing notching defects of dx152 hemizygotes. The double mutants show semi-lethality. Fusion of the fourth and fifth tarsal segments of the forelegs is seen in 60% of escapers, a phenotype that is not seen in either dx152 hemizygotes or Su(H)T4/+ animals.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments

dxTX0 completely rescues the wing, ocellus and ommatidial defects of dx152 mutants.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
References (8)