FB2025_01 , released February 20, 2025
Allele: Dmel\skdL7062
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General Information
Symbol
Dmel\skdL7062
Species
D. melanogaster
Name
FlyBase ID
FBal0087026
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
papL7062, l(3)L7062
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

Insertion of P{lacW} into the third skd intron, which falls in the coding region.

The P{lacW} insertion is 800bp downstream of the putative ATG start codon.

Allele components
Component
Use(s)
Inserted element
Encoded product / tool
Mutations Mapped to the Genome
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 ( 1 )
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

When heterozygous females are crossed to wild-type males, 22.7% of the heterozygous progeny have abdominal segmentation defects, while 9.5% of the +/+ offspring have defects.

No retinal phenotypes are seen in skdL7062 mutant flies.

The average number of crystal cells per embryo is reduced (to 9.9) in homozygous stage 13-14 embryos compared to wild type (36 +/- 2.2 cells on average). Mutant stage 14 embryos show cell cycle defects in the head region.

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

skdL7062 has visible | maternal effect | dominant phenotype, non-enhanceable by MED311/MED31[+]

Enhancer of
Statement
Reference

skdL7062 is an enhancer of visible | dominant phenotype of tna1

Suppressor of
Statement
Reference

skdL7062/skd[+] is a suppressor of visible | dominant phenotype of Bx1

Phenotype Manifest In
NOT Enhanced by
Statement
Reference

skdL7062 has adult abdomen | maternal effect phenotype, non-enhanceable by MED311/MED31[+]

Enhancer of
Statement
Reference
Suppressor of
Statement
Reference

skdL7062/skd[+] is a suppressor of wing margin phenotype of Bx1

Additional Comments
Genetic Interactions
Statement
Reference

When MED311/MED311 females are crossed to skdL7062/+ males, 54.7% of the MED311/skdL7062 adult progeny have abdominal defects, indicating that zygotic skdL7062 enhances the MED311 phenotype.

No increase in abdominal segmentation defects is seen in the adult progeny of MED311/skdL7062 females compared to the defects of the progeny of skdL7062/+ females, indicating that MED311 is not an enhancer of skdL7062 when maternally supplied.

Xenogenetic Interactions
Statement
Reference

One copy of skdL7062 enhances the retinal phenotype seen when Hsap\HTT128Q.1-336.Scer\UAS is expressed under the control of Scer\GAL4GMR.PU.

One copy of skdL7062 enhances the retinal phenotype seen when Hsap\ATXN182Q.Scer\UAS is expressed under the control of Scer\GAL4GMR.PU.

Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
Comments
Comments
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (8)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (9)