FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\kermitex31
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General Information
Symbol
Dmel\kermitex31
Species
D. melanogaster
Name
FlyBase ID
FBal0246013
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
dGIPCex31
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Cytology
Description

Imprecise excision of the progenitor insertion, resulting in a deletion that removes part of the kermit transcription unit (including the entire coding region), but does not affect the CG8709 gene.

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

Approximate endpoints of deletion resulting from the imprecise excision of P{EP}LpinEP2431. One endpoint is in the insertion. The other endpoint was estimated from an R5 coordinate scale and converted to R6 coordinates.

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

kermitex31/kermitex31, kermitex31/Df(2R)Exel7095 and kermitex31/Df(2R)ED1725 embryos exhibit significant numbers of abnormal motor axon pathways in both ISNb and SNa motor neurons. kermitex31/+ embryos exhibit a small increase in abnormal motor axon pathways in both ISNb and SNa motor neurons as compared to wild-type.

Homozygous clones do not result in wing hair defects.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
NOT Enhanced by
Suppressor of
Statement
Reference
Phenotype Manifest In
Enhanced by
NOT Enhanced by
Suppressor of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

kermitex31/+, Gyc76CKG03723ex173/+ double mutants, kermitex31/+, Sema-1ak13702/+ double mutants, and kermitex31/+, Df(4)C3/+ double mutants exhibit an increased number of defects in both ISNb and SNa motor neuron axon pathways as compared to kermitex31/+ mutant embryos.

kermitex31/kermitex31, Gyc76CKG03723ex173/Gyc76CKG03723ex173 double mutant embryos exhibit a similar number of defects in ISNb motor neuron pathways as compared to kermitex31/kermitex31 or Gyc76CKG03723ex173/Gyc76CKG03723ex173 single mutant embryos, and a similar number of defects in SNa motor neuron pathways as compared to kermitex31/kermitex31 single mutant embryos.

The multiple wing hair phenotype seen in flies expressing GαoGD8640 under the control of Scer\GAL4Bx-MS1096 is partially suppressed if they are heterozygous for kermitex31.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of kermitScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4elav.PU or Scer\GAL4sca-537.4 partially rescues the ISNb and SNa motor axon guidance defects of kermitex31/kermitex31 embryos.

Expression of kermitScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4repo or Scer\GAL4sim.PS fails to significantly rescue the ISNb and SNa motor axon guidance defects of kermitex31/kermitex31 embryos.

Expression of kermitScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4VGlut-OK371 significantly rescues the ISNb, but not SNa, motor axon guidance defects of kermitex31/kermitex31 embryos.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (4)