FB2024_03 , released June 25, 2024
Allele: Dmel\Ptp10D101
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General Information
Symbol
Dmel\Ptp10D101
Species
D. melanogaster
Name
FlyBase ID
FBal0104059
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Caused by aberration
Cytology
Description

Imprecise excision of the P{wAR} element resulting a deletion that removes most of the Ptp10D coding sequence (but not the first exon) and all of the bif coding sequence.

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
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Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
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Models Based on Experimental Evidence ( 0 )
Disease
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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
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External Data
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Phenotypic Class
Phenotype Manifest In
Other
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

The longitudinal axon bundles are irregular and often fuse to each other in Ptp10D101; Ptp69D1/Ptp69D8ex25 double mutant embryos. The outer Fas2-positive bundle is usually missing or reduced to short, discontinuous Fas2-positive regions, and breaks in the inner two bundles are also seen. Three or more Fas2-positive axon bundles that cross the midline are seen within the commissural tracts of each segment (this is not seen in wild-type embryos). Ptp69Dunspecified in double mutant combination with either Ptp10D1/Ptp10D101 or Df(1)101 results in alterations in many central nervous system axonal pathways in the embryo. The contralaterally projecting interneuronal axons of the NB 2-5 lineage cross the midline and turn anteriorly in a normal manner, but then double back across the midline after about two segments and grow posteriorly in the ipsilateral longitudinal tract. The axons of the ipsilateral intersegmental neurons grow anteriorly for a short distance and stop. The ISNd motorneuron extends an axon toward the midline that stalls and never enters the ISN root. In the NB 4-2 lineage, the RP2 axons stall before reaching their target, and the CoR axons do not branch onto all of their target muscles. The projection of local interneurons across the midline in the anterior commissure appears wild type, except that the axons always defasciculate into two bundles after crossing the midline. Ectopic interneuronal projections form on the ipsilateral side, and project across segmental boundaries in the anterior direction (these axons never form in wild type). In the NB 3-1 lineage, the RP neurons (RP1, RP3, RP4 and RP5) extend axons normally across the commissure and into the ISNb nerve, although they do not form normal synapses. The interneuronal projections are radically altered; they still cross the midline, but do not form defined anterior and posterior projections in the contralateral connective. Instead, they grow anteriorly in a circular path around the neuropil, contacting the midline at the end of their trajectory. No alterations in the numbers or positions of cell bodies of the progeny of NBs 3-1, 4-2 or 2-5 are seen in these embryos. Fas2-positive axons are seen crossing the midline in 95.5% of segments in Ptp10D1/Ptp10D101; Ptp69D4/Ptp69D8ex25 double mutant embryos (this is never seen in wild-type embryos).

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
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Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Ptp10D101
Name Synonyms
Secondary FlyBase IDs
    References (1)