FB2025_01 , released February 20, 2025
Allele: Dmel\Cad99C120B
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General Information
Symbol
Dmel\Cad99C120B
Species
D. melanogaster
Name
FlyBase ID
FBal0270002
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Cytology
Description

Imprecise excision of the progenitor insertion, resulting in a deletion that removes part of Cad99C, spanning from 4999bp 5' to 75bp 5' of the translation start codon.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Comment:

Deletion resulting from the imprecise excision of P{EP}Cad99CGE23478, which removes sequences from 4999bp 5' to 75bp 5' of the Cad99C translation start codon.

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

Most embryos from Cad99C57A/Cad99C120B females are not recoverable. Most (>90%) of these maternal and zygotic (M/Z)Cad99C-expressed embryos develop normally but have longer, thinner salivary glands than in wild-type; only a small subset of the recovered embryos show severe morphological defects. Embryos missing only maternal or only zygotic function do not have overt defects. No phenotypic differences are detected at the ultrastructural level in comparisons of stage 15/16 Cad99C[M/Z] mutant and wild-type salivary glands. The overall polarity of Cad99C[MZ] mutant salivary glands appear unaffected and the mutant salivary glands migrate normally, contacting the same tissues at all stages as wild-type salivary glands. Total cell numbers are not significantly different and the apical domain size and elongation ratio of individual cells is also unchanged. Indeed, the only difference is that fewer cells surround the lumen in cross-sections of the Cad99C[M/Z] mutant salivary glands compared with wild-type. Thus, the longer, thinner salivary gland lumen in Cad99C[M/Z] mutants reflect differences in cell rearrangement during tube elongation.

Eggs laid by homozygous females spontaneously collapse after deposition and do not develop into larvae. These eggs are nearly all permeable to the dye Neutral Red after dechorionation, suggesting a vitelline membrane defect.

More than 80% of eggs laid by Cad99C57A/Cad99C120B and Cad99C51C/Cad99C120B females are permeable to the dye Neutral Red after dechorionation, suggesting a vitelline membrane defect.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Suppressor of
Additional Comments
Genetic Interactions
Statement
Reference

Cad99C57A/Cad99C120B significantly rescues the salivary gland defects of AdamTS-AKO/Df(3R)88F5 embryos.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (3)