FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
Allele: Dmel\Idh3b2
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General Information
Symbol
Dmel\Idh3b2
Species
D. melanogaster
Name
FlyBase ID
FBal0123174
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Amino acid replacement: G278D.

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

G22017390A

Reported nucleotide change:

G?A

Amino acid change:

G278D | Idh3b-PA; G278D | Idh3b-PB

Reported amino acid change:

G278D

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

Idh3b2/Df(3R)Exel6188 transheterozygotes develop more slowly relative to controls as the time from egg-laying to puparium formation is significantly increased; the anterior spiracle eversion is often impaired and many puparia resemble sclerotized larvae, the mutant pupae also show abnormal persistence of larval salivary glands in the pupal stage (beyond 30 hr after puparium formation). The mitochondria in late/pupae and prepupae do not undergo fragmentation as is typical for wild-type but rather clamp together and remain elongated.

Embryos from mothers with germline consisting of solely Idh3b2 mutant cells (created by the ovoD technique) arrest development in embryonic stage, their nuclei are highly variable in size and often incompletely separated.

Mutant salivary gland cells contain large eosin positive vacuoles and plasma membranes and show variable chromosome banding - phenotypes associated with delaying salivary gland programmed cell death due to a failure in the onset of autophagy.

Idh3b2/Idh3b1 mutants fail to shorten their bodies properly at puparium formation, fail to tan, often exhibit a defect in anterior spiracle eversion and die following head eversion. Mutants possess persistent salivary glands, even though adult structures have formed, including eyes and wings.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

The Eip93FΔ1 allele successfully complements Idh3b2 (from the former 'E93[1-3]' complementation group).

The lethality of Idh3b2/Df(3R)Exel6188 transheterozygous mutants as well as the abnormal persistence of their larval salivary gland during pupal stages is rescued by combination with a single copy of Idh3b+t3.0.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Eip93F2
Name Synonyms
Secondary FlyBase IDs
    References (3)