FB2024_03 , released June 25, 2024
Allele: Dmel\S05671
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General Information
Symbol
Dmel\S05671
Species
D. melanogaster
Name
FlyBase ID
FBal0030177
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
S5671
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description
Allele components
Component
Use(s)
Inserted element
Encoded product / tool
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

Heterozygous animals show a weak rough eye phenotype, with ommatidia showing both rotation and recruitment defects.

Heterozygous adults exhibit some weakly misrotated ommatidia, as well as a defect in photoreceptor cell recruitment.

Heterozygotes have a missing-bract phenotype (31% of bracts in the tibia and 89% in the basitarsus of the second leg remain).

Adults exhibit rough eyes.

Clonal analysis reveals mutant phenotypes in photoreceptor cells and wing veins.

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

S05671 has abnormal cell polarity phenotype, non-enhanceable by mys1

NOT suppressed by
Statement
Reference

S05671 has abnormal cell polarity phenotype, non-suppressible by mys1

S05671 has abnormal cell polarity phenotype, non-suppressible by wb09437

Enhancer of
Statement
Reference

S05671 is an enhancer of visible | dominant phenotype of KrIf-1

Other
Phenotype Manifest In
Enhanced by
Statement
Reference

S05671 has eye phenotype, enhanceable by Df(3L)Krn260/Df(3L)Krn260

S05671 has ommatidium phenotype, enhanceable by shg2

S05671 has ommatidium phenotype, enhanceable by shgk03401

S05671 has ommatidium phenotype, enhanceable by spiSCP1/spi[+]

S05671 has photoreceptor phenotype, enhanceable by spiSCP1/spi[+]

S05671 has ommatidium phenotype, enhanceable by shg1

S05671 has mesothoracic tarsal segment 1 & bract phenotype, enhanceable by Ras85De1B

S05671 has mesothoracic tibial bract phenotype, enhanceable by Ras85De1B

NOT Enhanced by
Statement
Reference

S05671 has ommatidium phenotype, non-enhanceable by mys1

S05671 has ommatidium phenotype, non-enhanceable by wb09437

NOT suppressed by
Statement
Reference

S05671 has ommatidium phenotype, non-suppressible by mys1

S05671 has ommatidium phenotype, non-suppressible by wb09437

Enhancer of
Statement
Reference

S05671 is an enhancer of eye phenotype of DCTN1-p150Gl-1

S05671 is an enhancer of mesothoracic tarsal segment 1 & bract phenotype of Ras85De1B

S05671 is an enhancer of bract phenotype of Ras85De1B

S05671 is an enhancer of eye phenotype of KrIf-1

S05671 is an enhancer of ommatidium phenotype of KrIf-1

S05671 is an enhancer of eye phenotype of bunrI043

Suppressor of
Statement
Reference

S05671 is a suppressor of phenotype of rhohs.sev

Other
Additional Comments
Genetic Interactions
Statement
Reference

Dhc64Cγ4163a S05671 and Dhc64C6-10 S05671 transheterozygotes have an incomplete L5 wing vein which does not reach the wing margin.

S05671/+, Df(3L)Krn260/Df(3L)Krn260 flies show a stronger rough eye than S05671/+ alone, with many more ommatidia being misrotated. Occasional achiral ommatidia are observed.

S05671/+, Df(3L)Krn-27-7-B/Df(3L)Krn-27-7-B flies show a severe enhancement of the S05671/+ eye phenotype. Both ommatidial rotation and recruitment defects are observed, with many ommatidia having too few photoreceptors. Occasional achiral ommatidia are observed.

Scer\GAL4GMR.PF-driven expression of KrndsRNA.Scer\UAS enhances the S05671/+ eye phenotype. Both ommatidial rotation and recruitment defects are observed. Around 2% of ommatidia have too many photoreceptors. Occasional achiral ommatidia are observed.

Heterozygosity for spiSCP1 enhances both the photoreceptor cell recruitment and misrotation phenotypes seen in S05671/+ animals. Heterozygous wb09437 or mys1 has no effect on the S05671/+ ommatidial polarity phenotype. Heterozygous shg1, shgk03401, or shg2 significantly enhances the ommatidial misrotation phenotype seen S05671/+ animals.

Ras85De1B/+, S05671/+ double mutants have a stronger missing-bract phenotype than either mutant alone. (2% of bracts in the tibia and 60% in the basitarsus of the second leg remain). The addition of Ras85Dhs.M11.2 under heat shock control partially suppresses this phenotype.

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

Spradling group.

Comments
Comments

Excision of the P{PZ} element results in viability demonstrating the insertion to be responsible for lethality.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
Reported As
Name Synonyms
Secondary FlyBase IDs
  • FBal0045045
References (14)