FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\PGRP-LC2
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General Information
Symbol
Dmel\PGRP-LC2
Species
D. melanogaster
Name
FlyBase ID
FBal0137406
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
PGRP2
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: ??term.

Stop codon is introduced into the PGRP-LCx isoform, resulting in a truncated protein lacking the last 107 amino acids of this isoform.

Nucleotide substitution: G?A.

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

G9345880A

Reported nucleotide change:

G?A

Amino acid change:

W392term | PGRP-LC-PA; W392term | PGRP-LC-PD; W221term | PGRP-LC-PE

Reported amino acid change:

??term

Comment:

Mapped site of nonsense mutation based on report that it removes the last 107 amino acids of isoform PGRP-LCx, which appears to correspond to annotated isoforms PGRP-LC-PA. The G to A change may occur at the second or third base of the Trp codon to give a nonsense mutation. The exact site of mutation was not specified.

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

Motor neurons in PGRP-LC2/+ third instar larvae show similar mEPSP (mini excitatory postsynaptic potential) and EPSP (excitatory postsynaptic potential) amplitudes and quantal content as controls.

The neuromuscular junctions of PGRP-LC2 homozygous mutant third instar larvae present small but significant decreases in spontaneous miniature excitatory postsynaptic potential and in excitatory postsynaptic potential, but no significant changes in quantal content, as compared to controls.

The neuromuscular junctions of PGRP-LCΔE/PGRP-LC2 transheterozygous mutant third instar larvae present small but significant decrease in spontaneous miniature excitatory postsynaptic potential and increase in quantal content, but no significant effect in the excitatory postsynaptic potential, as compared to controls.

PGRP-LC2 heterozygosity has no significant effect on either spontaneous miniature excitatory postsynaptic potential, excitatory postsynaptic potential or quantal content of third instar larval neuromuscular junctions, as compared to controls.

The neuromuscular junction of PGRP-LC2 homozygous mutant third instar larvae shows similar overall structure to controls, with similar number of synaptic boutons, similar number and length of active zones, similar average vesicle number, similar vesicle diameter, similar average vesicle distance from the T-bar centroid.

Blood cells from mutant animals can phagocytose bacteria.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (3)