FB2024_03 , released June 25, 2024
Allele: Dmel\cdiR47
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General Information
Symbol
Dmel\cdiR47
Species
D. melanogaster
Name
FlyBase ID
FBal0123023
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Caused by aberration
Cytology
Description

2.077bp deletion that removes the first exon of cdi and removes the mRpL55 gene.

Imprecise excision of the P-element resulting in a 2.1kb deletion which removes cdi sequences. The open reading frame of the neighbouring ATPsyn-d gene is unaffected by this deletion.

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

F-actin distribution is irregular, granulated and disorganised in homozygous Df(3R)cdiR47 clones in the eye disc in which mRpL55 function has been restored by expression of mRpL55Scer\UAS.cSa under the control of Scer\GAL4GMR.PU. These defects are less evident in mosaic ommatidia composed of both mutant and wild-type cells.

Mutants have an affected nervous system.

Although the reading frame of the neighbouring ATPsyn-d gene is unaffected in the "cdiR47" mutant chromosome, it remains possible that its function could be affected, thus it is unclear whether the lethality of the "cdiR47" mutant chromosome is due to an affect on cdi or ATPsyn-d.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhancer of
Statement
Reference

cdiR47/cdi[+] is an enhancer of male semi-sterile phenotype of Rac1J11

Other
Statement
Reference
Phenotype Manifest In
Other
Statement
Reference

Rac1J11, cdiR47/cdi[+] has testis phenotype

Additional Comments
Genetic Interactions
Statement
Reference

74% of Rac1J11 cdiR47/Rac1J11 males are sterile in individual crosses with females. The males have an abnormal accumulation of dense material in the distal part of the testis.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer

Selected as: flies which have lost the ry+ eye colour marker of the P-element progenitor (P{lacZ}cdi87 or P{FZ}cdi242).

Comments
Comments

"FBti0009052 == P{lacZ}cdi87" was stated as tentative. "FBti0003444 == P{FZ}cdi242" was stated as tentative.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (5)