FB2024_03 , released June 25, 2024
Allele: Dmel\mlt4210
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General Information
Symbol
Dmel\mlt4210
Species
D. melanogaster
Name
FlyBase ID
FBal0090223
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

Insertion at nucleotide 2R:6046076 (release 5 coordinates), within a region common to the 5' UTR of all three mlt isoforms.

Allele components
Component
Use(s)
Inserted element
Encoded product / tool
Mutations Mapped to the Genome
Curation Data
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

Individualisation complexes assembled around spermatid nuclear bundles are intact in mltEY02157/mlt4210 testes, but progressed individualisation complexes (those no longer co-localising with the nuclear bundle) are often disrupted, having one or more investment cones out of register. Sleeves of F-actin associated with highly condensed spermatid bundles at the most basal end of the testis tubule are sometimes seen.

Mutants show male sterility, with highly elongated, immobile, blebbed sperm tails and altered individualisation complexes. Individualisation complexes form normally but degrade as they proceed caudally along the cyst.

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

Mutation is revertible on introduction of P{Δ2-3}.

Although the P{lacW}mlt4210 insertion maps within both 5'UTR of the CG12214 annotation and an intron of KCNQ (nested genes, CG12214 is entirely within a large intron of KCNQ), complementation analysis indicates that the "mlt" mutant phenotype caused by this insertion (spermatid individualisation defects) is due to an effect on CG12214 and not on KCNQ.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
mlt4210
Name Synonyms
Secondary FlyBase IDs
    References (2)