FB2025_01 , released February 20, 2025
Allele: Dmel\aopA141
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General Information
Symbol
Dmel\aopA141
Species
D. melanogaster
Name
FlyBase ID
FBal0042848
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
yanP
Key Links
Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description

P-element insertion within an intron.

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

aopyan-1/aopA141 eye discs show chirality defects in 9.4% of ommatidial clusters.

aopA141 mutants exhibit on average 37% extra R7 cells.

Homozygotes exhibit 20% mutant ommatidia.

Eyes are mildly rough, only 20% ommatidia contain extra R7 cells.

Rough eye phenotype due to supernumerary R7 cells.

Almost wild type external appearance of the eye.

Homozygotes have reduced viability and fertility. Weak rough eye phenotype, 20% of ommatidia contain at least one extra photoreceptor.

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

aopA141 has visible phenotype, enhanceable by ttk55.3

aopA141 has visible phenotype, enhanceable by Dp(1;2)51b

Suppressed by
Statement
Reference

aopA141 has visible phenotype, suppressible by N55e11

Phenotype Manifest In
Enhanced by
Statement
Reference

aopA141 has ommatidium phenotype, enhanceable by Su(H)del47

aopA141 has photoreceptor cell R7 phenotype, enhanceable by ttk55.3

aopA141 has phenotype, enhanceable by ttk[+]/ttk00219

aopA141 has phenotype, enhanceable by ttk[+]/ttkrM730

aopA141 has phenotype, enhanceable by Df(3R)ttk-Δ4/+

aopA141 has ommatidium phenotype, enhanceable by Dp(1;2)51b

aopA141 has eye phenotype, enhanceable by RasGAP1rI533

aopA141 has ommatidium phenotype, enhanceable by RasGAP1rI533

Suppressed by
Statement
Reference

aopA141 has ommatidium phenotype, suppressible by pnt07825Δ78

aopA141 has ommatidium phenotype, suppressible by N55e11

Enhancer of
Statement
Reference

aopA141 is an enhancer of phenotype of svp2.sev

aopA141 is an enhancer of phenotype of svp1.sev

aopA141 is an enhancer of eye phenotype of rhohs.sev

Suppressor of
Statement
Reference

aopA141 is a suppressor of photoreceptor cell R7 phenotype of SosJC2, sev6

Other
Additional Comments
Genetic Interactions
Statement
Reference

Homozygous aopA141 mutants, with one copy of alphS-331 exhibit an increase from 37% to 86% in the number of extra R7 cells. Double homozygotes exhibit extra R7 cells in all ommatidia, with an average of almost three R7 cells per ommatidium, which visibly increases eye roughness.

Double homozygotes of alphc04528 and aopA141 exhibit extra R7 cells in all ommatidia, with an average of almost three R7 cells per ommatidium, which visibly increases eye roughness.

The addition of Su(H)del47 to aopA141 homozygotes leads to 44% of ommatidia being mutant. The addition of Su(H)del47 to pnt07825Δ78 homozygotes leads to 1.3% of ommatidia being mutant.

Loss of wild type ttk enhances the phenotype so up to 75% ommatidia contain extra R7 cells.

Enhancer of the dosage-dependent (two or more copies of P{sev-svp1} or P{sev-svp2}) transformation of cone cells into R7 photoreceptors and at a lower frequency R7 cells into outer photoreceptors.

sev6/sev+; SosJC2/aopA141 mutants exhibit an increase in the number of R7 cells compared to sev6/SosJC2 mutants with two functional aop copies. Transheterozygotes with Dp(1;2)51b exhibit enhancement of the rough eye phenotype and transheterozygotes with N55e11 exhibit suppression of the mutant eye phenotype.

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

Mutant phenotype of aopA141 can be reverted by excision of the P-element.

Weak aop mutation.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
References (11)