FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Cenp-Cprl41
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General Information
Symbol
Dmel\Cenp-Cprl41
Species
D. melanogaster
Name
FlyBase ID
FBal0031912
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
l(3)85Aaprl41, Cenp-Cpr141
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Amino acid replacement: Q1107term.

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

C8567838T

Amino acid change:

Q1107term | Cenp-C-PA; Q1095term | Cenp-C-PB

Reported amino acid change:

Q1107term

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

mitotic anaphase & nuclear chromosome

mitotic telophase & nuclear chromosome

Detailed Description
Statement
Reference

Cenp-Cprl41/Df(3R)p25 animals show defects in the central nervous system (CNS) during the second half of embryogenesis; the CNS contains many oversize cells and has more apoptotic cells than normal. Mitosis 16 is severely abnormal in Cenp-Cprl41 embryos; while metaphase figures appear relatively normal, anaphase and telophase figures often have abnormal chromatin bridges.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
NOT suppressed by
Statement
Reference

Cenp-Cprl41 has lethal | recessive phenotype, non-suppressible by CG11737t15

Cenp-Cprl41 has lethal | recessive phenotype, non-suppressible by CG31259t15

Cenp-Cprl41 has lethal | recessive phenotype, non-suppressible by pch2t6.4

Cenp-Cprl41 has lethal | recessive phenotype, non-suppressible by CG31454t15

Cenp-Cprl41 has lethal | recessive phenotype, non-suppressible by CG31460t6.4

Cenp-Cprl41 has lethal | recessive phenotype, non-suppressible by mRpS18Ct6.4

Enhancer of
Statement
Reference

Cenp-C[+]/Cenp-Cprl41 is an enhancer of visible phenotype of Scer\GAL4GMR.PF, pimUAS.Tag:MYC

Cenp-C[+]/Cenp-Cprl41 is an enhancer of visible phenotype of thrΔC.GMR.Tag:MYC

Phenotype Manifest In
Enhancer of
Statement
Reference

Cenp-C[+]/Cenp-Cprl41 is an enhancer of eye phenotype of Scer\GAL4GMR.PF, pimUAS.Tag:MYC

Cenp-C[+]/Cenp-Cprl41 is an enhancer of eye phenotype of thrΔC.GMR.Tag:MYC

Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
References (10)