FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\gekNP5192
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General Information
Symbol
Dmel\gekNP5192
Species
D. melanogaster
Name
FlyBase ID
FBal0222341
Feature type
allele
Associated gene
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Carried in Construct
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    Phenotypic Data
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    Homozygous gekNP5192 mutants exhibit highly penetrant R cell targeting phenotypes.

    In homozygous gekNP5192 and transheterozygous gekNP5192/Df(2R)e03819-f02302 animals R cell axon fascicles above the lamina plexus are occasionally clumped and the lamina plexus appears broken and varies in thickness. This phenotype is seen in all brains examined. Additionally, occasional bundles of axons were observed extending into the medulla that are thicker than usual. Organisation of the lamina neurons in homozygous gekNP5192 eye discs is normal. Glial cells migrate normally into the lamina and are only subtly disorganised, likely a consequence of the clumping of R1-R6 terminals in the lamina plexus.

    In homozygous gekomb1080/gekNP5192 third instar larvae R cell axon fascicles above the lamina plexus are occasionally clumped and the lamina plexus appears broken and varies in thickness. This phenotype is seen in all brains examined. Additionally, occasional bundles of axons were observed extending into the medulla that are thicker than usual.

    Homozygous gekNP5192 photoreceptor clones extend out of the retina into the brain, fasciculate normally and stop in the lamina. However, once in the lamina, mutant photoreceptors often make errors in columnar targeting, making projections to one or more incorrect target cartridges in addition to the correct target, or failing to extend at all.

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      References (2)