FB2026_02 , released June 18, 2026
Allele: Dmel\lin-281
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General Information
Symbol
Dmel\lin-281
Species
D. melanogaster
Name
FlyBase ID
FBal0346050
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Deletion that removes most of the exons of lin-28 (all except the first exon are deleted). The deletion ends immediately upstream of the downstream sif gene, and mRNA expression levels are similar to that of wild-type. Generated by imprecise excision of P{EP}lin-28EP915.

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

1541bp deletion resulting from the imprecise excision of P{EP}lin-28EP915 that removes most of the lin-28 coding region. The deletion ends immediately upstream of the downstream sif gene.

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

lin-281/lin-281 embryos do not show any defects in the central nervous system (as shown by Mef2 and Pericardin immunostaining patterns) and hatch at comparable rates to controls.

lin-281/lin-281 and lin-281/Df(3L)Exel6106 adult male and female flies do not show significant changes in body weight, as compared to controls.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

lin-281/lin-281, pnrVX6/+ mutant embryos do not show any defects in the central nervous system (as shown by Mef2 and Pericardin immunostaining patterns), as compared to controls.

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 (1)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (2)