FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\mysM2
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General Information
Symbol
Dmel\mysM2
Species
D. melanogaster
Name
FlyBase ID
FBal0138198
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: Q66term.

Nucleotide substitution: C196T.

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

C8064153T

Reported nucleotide change:

C196T

Amino acid change:

Q66term | mys-PA; Q66term | mys-PB; Q66term | mys-PC; Q66term | mys-PD

Reported amino acid change:

Q66term

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

Adult-generated mysM2 homozygous mutant intestinal stem cell clones have reduced maintenance 7 days and 14 days after clone induction compared to control clones; remaining clones contain fewer cells by day 14 and many only contain differentiated cells; enteroendocrine cell/enterocyte ratio is unaffected and intestinal stem cells show no obvious signs of apoptosis.

Loss of mys in mysM2 mutant clones results in scars forming in the underlying basement membrane, indicating that integrins are involved in the capture by tissues of Collagen IV from the contacting haemolymph.

mysM2 dorsal branch terminal cell clones in third instar larvae show substantial branch pruning and multiple convoluted lumens coursing through the remaining terminal branches.

Homozygous somatic clones in the wing result in wing blisters. Mutant embryos show dorsal herniation. mysb7/mysM2 animals show 92% viability.

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

Adult posterior midguts from mysM2/+; Itgbn1/Itgbn1 have a similar proportion of intestinal stem cells to Itgbn1 heterozygotes and homozygotes.

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
Name Synonyms
Secondary FlyBase IDs
    References (6)