FB2024_03 , released June 25, 2024
Allele: Dmel\LarC219
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General Information
Symbol
Dmel\LarC219
Species
D. melanogaster
Name
FlyBase ID
FBal0128170
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: Q559term.

Nucleotide substitution: C?T.

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

C19717196T

Reported nucleotide change:

C?T

Amino acid change:

Q559term | Lar-PA; Q541term | Lar-PB; Q541term | Lar-PD; Q564term | Lar-PF; Q564term | Lar-PG; Q556term | Lar-PH; Q570term | Lar-PI

Reported amino acid change:

Q559term

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

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

photoreceptor cell R7 & axon | somatic clone

Detailed Description
Statement
Reference

Mosaic animals in which the retina is homozygous (generated using the "eyFLP" system) show photoreceptor projection defects. The R1-R6 and R8 axons all terminate in their correct target layers. R7 axons reach the medulla, but most stop short of their normal target, generally stopping in the same layer as the R8 axons. 40% of homozygous R7 photoreceptor axons in a Lar+ background (generated using P{GMR-FLP1.P}) terminate in the same layer as R8 axons, with the remaining 60% terminating in or near their correct target layer, though some termini have abnormally thin and extended morphology. 93% of homozygous R7 photoreceptor axons in a Lar+ background generated using P{ey-FLP.N} show mistargeting of R7 axons. The difference in frequency of mistargeting may be due to perdurance of Lar+ protein in homozygous R7 cells induced by P{GMR-FLP1.P} (which induces clones later than P{ey-FLP.N}) or it may reflect a non-autonomous function of Lar+ in R8 cells, since in clones generated by P{GMR-FLP1.P} R8 is Lar+ while in most clones generated by P{ey-FLP.N} R8 is also Lar-.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Suppressed by
Statement
Reference

LarC219 has photoreceptor cell R7 & axon | somatic clone phenotype, suppressible by Lar::Ptp69DLP.GMR.Tag:SS(wg),Tag:HA

NOT suppressed by
Statement
Reference

LarC219 has photoreceptor cell R7 & axon | somatic clone phenotype, non-suppressible by Lar::Ptp69DPL.GMR.Tag:SS(wg),Tag:HA

LarC219 has photoreceptor cell R7 & axon | somatic clone phenotype, non-suppressible by Ptp69DGMR.Tag:SS(wg),Tag:HA

Additional Comments
Genetic Interactions
Statement
Reference

Ptp69DGMR.T:wg,T:Ivir\HA1 or Lar::Ptp69DPL.GMR.T:wg,T:Ivir\HA1 do not rescue the R7 targeting defects of mosaic animals in which the retina is homozygous for LarC219. Lar::Ptp69DLP.GMR.T:wg,T:Ivir\HA1 rescues the R7 targeting defects of mosaic animals in which the retina is homozygous for LarC219. The targeting defects of Ptp69DD1689 R7 axons are rescued by LarGMR.T:wg,T:Ivir\HA1.

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

Selected as: a mutation that results in photoreceptor projection defects in mosaic animals in which the retina, but no other tissue is homozygous.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (1)