FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\CG35111
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General Information
Symbol
Dmel\CG35111
Species
D. melanogaster
Name
FlyBase ID
FBal0156993
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

Nucleotide substitution: C569T. Nucleotide substitution: A570G. In addition to the two missense mutations, there is a single base pair deletion at nucleotide 572. These changes are predicted to cause a frameshift at amino acid 133 and the early truncation of the protein at residue 158.

Nucleotide substitution: C578T. Nucleotide substitution: A579G. 1 bp deletion of C581. Amino acid replacement: N133E. Frameshift causes 24 novel amino acids before a stop codon.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Reported amino acid change:

N133E|CG3511-PA

Comment:

Deletion of a single C residue leads to a frameshift and truncation of the CDS after 24 novel amino acids. Two missense mutations are also observed in CG35111.

Nucleotide change:

C24572408T

Reported nucleotide change:

C569T

Amino acid change:

T132T | CG3511-PA; T132T | CG3511-PB

Reported amino acid change:

T133T

Comment:

One of two missense mutations observed in CG35111. In addition, a single base is deleted leading to a frameshift.

Nucleotide change:

A24572409G

Reported nucleotide change:

A570G

Amino acid change:

N133D | CG3511-PA; N133D | CG3511-PB

Reported amino acid change:

N133E

Comment:

One of two missense mutations observed in CG35111. In addition, a single base is deleted in same codon leading to a frameshift.

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

Homozygous clones in the eye induced in an Rbf+ background are viable. Homozygous larvae have an enlarged body phenotype compared to their heterozygous siblings. These "large larvae" wander for an extended period before death, although rare escapers can progress to giant pupae that fail to eclose as adults.

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

Homozygous CG35111 clones induced in the eye in a RbfSLS-15 background do not survive.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

Selected as: a mutation that results in synthetic cell lethality in clones in the eye in a RbfSLS-15 background.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
CG35111
Name Synonyms
Secondary FlyBase IDs
    References (2)