FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\ana2169
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General Information
Symbol
Dmel\ana2169
Species
D. melanogaster
Name
FlyBase ID
FBal0269126
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: L222term.

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

T8899456A

Amino acid change:

L222term | ana2-PA; L222term | ana2-PB

Reported amino acid change:

L222term

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
Detailed Description
Statement
Reference

ana2169/ana2719 adults are uncoordinated and fail to perform in climbing assay (negative gravitaxis assay) when compared to controls.

Homozygous larvae have an increased number of neuroblasts in the central brain at 96 hours after larval hatching (approximately 250 neuroblasts compared to approximately 100 neuroblasts in wild-type larvae at this stage). The number of mushroom body neuroblasts appears to be increased approximately 5-fold in the mutant compared to wild type. Approximately 10% of homozygous neuroblasts divide symmetrically into two similar-sized daughter cells. Astral microtubules are absent in the mutant neuroblasts.

17% of homozygous larval brain clones transplanted into the abdomens of wild-type hosts form tumours, proliferating massively and killing the hosts rapidly. 100% of the mutant tissue develops tumours in subsequent rounds of transplantation.

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

Expression of ana2N1.Scer\UAS.T:Avic\GFP-YFP.Venus under the control of Scer\GAL4insc-Mz1407 almost fully rescues the centrosome assembly and spindle orientation defects of ana2169/ana2719 neuroblasts.

Expression of either ana2C1.Scer\UAS.T:Avic\GFP-YFP.Venus, ana2N2.Scer\UAS.T:Avic\GFP-YFP.Venus or ana2C2.Scer\UAS.T:Avic\GFP-YFP.Venus under the control of Scer\GAL4insc-Mz1407 fails to rescue the spindle orientation defects of ana2169/ana2719 neuroblasts.

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 (6)