FB2024_03 , released June 25, 2024
Allele: Dmel\w69C
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General Information
Symbol
Dmel\w69C
Species
D. melanogaster
Name
FlyBase ID
FBal0146688
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

P{GMroX1} insertion in the second intron of ara.

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

Eye colour: the dorsal 30% of the eye is pigmented in hemizygotes of both sexes, but the ventral 70% is completely white in females and sectored in males carrying one copy of w69C in a w- background. Males homozygous for w69C in a w- background have eyes with nearly solid red pigmentation with a lighter equator. About 10% of females homozygous for w69C in a w- background have a small pigmented sector in the ventral half of the eye.

Eye colour: females carrying w69C in a w- background only show expression of w in the dorsal part of the eye (w expression is silenced in the ventral 70% of the eye). Eye colour: males carrying w69C in a w- background show expression of w in the dorsal part of the eye and in addition have sporadic red sectors in the ventral part of the eye.

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

w69C has abnormal eye color | male phenotype, suppressible by Pc3

w69C has abnormal eye color | female phenotype, suppressible by Pc3

NOT suppressed by
Statement
Reference
Phenotype Manifest In
NOT Enhanced by
Statement
Reference

w69C has pigment cell | female phenotype, non-enhanceable by Df(1)52/lncRNA:roX1ex6

Suppressed by
Statement
Reference

w69C has eye | ventral | female phenotype, suppressible by Pc3

w69C has eye | ventral | male phenotype, suppressible by Pc3

w69C has pigment cell | female phenotype, suppressible by Pc3

w69C has pigment cell | male phenotype, suppressible by Pc3

w69C has pigment cell | male phenotype, suppressible by Df(1)52/lncRNA:roX1ex6

NOT suppressed by
Statement
Reference

w69C has pigment cell | female phenotype, non-suppressible by Df(1)52/lncRNA:roX1ex6

Additional Comments
Genetic Interactions
Statement
Reference

Pc3 results in a weak derepression of w expression in the ventral part of the eye in both males and females carrying one copy of w69C in a w- background.

Eye colour: the expression of w69C in females carrying w69C in a w- background is unchanged if they are also carrying roX1ex6 Df(1)52 P{w+4Δ4.3}. Eye colour: males carrying w69C in a w- background that are also carrying roX1ex6 Df(1)52 P{w+4Δ4.3} show almost complete derepression of w69C expression in the ventral part of the eye.

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 (1)
Reported As
Symbol Synonym
w69C
Name Synonyms
Secondary FlyBase IDs
    References (2)