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General Information
Symbol
Dmel\dallyMH32
Species
D. melanogaster
Name
FlyBase ID
FBal0192041
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
dally32
Nature of the Allele
Mutations Mapped to the Genome
 
Type
Location
Additional Notes
References
Associated Sequence Data
DNA sequence
Protein sequence
 
 
Cytology
Nature of the lesion
Statement
Reference

Imprecise excision of the P{GSV6}9068 insertion has created a 1.8kb deletion that removes the first exon of the dally gene, which includes the translation start site.

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 )
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Mutant animals exhibit notches in the wing at a low frequency (5%) this frequency is increased in animals (41%) also missing the maternal component.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
NOT Enhancer of
Statement
Reference

dallyMH32 is a non-enhancer of visible | recessive phenotype of magu2

NOT Suppressor of
Statement
Reference

dallyMH32 is a non-suppressor of visible | recessive phenotype of magu2

Phenotype Manifest In
Enhancer of
Statement
Reference
NOT Enhancer of
Statement
Reference

dallyMH32 is a non-enhancer of wing vein L5 phenotype of magu2

NOT Suppressor of
Statement
Reference

dallyMH32 is a non-suppressor of wing vein L5 phenotype of magu2

Additional Comments
Genetic Interactions
Statement
Reference

The wing defects seen in magu2, dallyMH32 double mutants appear similar to the lateral patterning defects of magu2 single mutants.

Embryos mutant for both zygotic and maternal dlpMH20 and dallyMH32 (dlpMH20, dallyMH32) exhibit a denticle phenotype stronger than seen in dallyMH32 mutants and exhibit mid-ventral denticle whorls.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
References (8)