FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\IncenpEC3747
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General Information
Symbol
Dmel\IncenpEC3747
Species
D. melanogaster
Name
FlyBase ID
FBal0221166
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
Cytology
Description

Amino acid replacement: Q457term.

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

C7280291T

Reported nucleotide change:

C?T

Amino acid change:

Q458term | Incenp-PA; Q458term | Incenp-PB; Q458term | Incenp-PC

Reported amino acid change:

Q457term

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

Expression of IncenpUASp.Tag:MYC under the control of Scer\GAL4VP16.nos.UTR leads to abnormal chromosome segregation (including missegregation of both chiasmate and achiasmate X chromosomes) in oocytes although a bipolar spindle forms in most of the oocytes as compared to controls. There are more severe defects in a IncenpEC3747 background.

IncenpEC3747 mutant first larval instar escapers show reduced mobility and abnormal wandering behaviour.

Heterozygous IncenpEC3747 mutants exhibit a wild-type neural pattern in the PNS.

Homozygous IncenpEC3747 mutants exhibit a range of neural defects in the PNS, from severe cases of neuronal loss to perturbation of the neural clusters and missing subsets of neurons.

There appears to be no difference between IncenpEC3747 mutant and wild-type embryos during the first 13 rapid synchronous cycles. IncenpEC3747 embryos show no defect in cellularization. There are no defects in early-stage embryos, although from mitotic cycle 15, a very low percentage of cells exhibit chromosome segregation defects. By embryonic stage 13, cells in the central nervous system show enlarged nuclei and bigger or multiple centrosomes compared with wild-type.

IncenpEC3747 neuroblasts exhibit defects in the shape and orientation of the basal pros cresent.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhancer of
Statement
Reference

IncenpEC3747/Incenp[+] is an enhancer of abnormal mitotic cell cycle phenotype of sub131/sub1

Other
Statement
Reference
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

sub1/sub131, IncenpEC3747/+ mutant larval brains display defects in spindle assembly, and short and disorganised metaphase spindles are common. Anaphase spindles usually lack an organised midzone, and 76% show lagging chromosomes at anaphase (compared to 55% in sub1/sub131 mutant brains). Double mutant larvae exhibit a high frequency of polyploid cells.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Fails to complement
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (4)