FB2024_03 , released June 25, 2024
Allele: Dmel\NCo
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General Information
Symbol
Dmel\NCo
Species
D. melanogaster
Name
Confluens
FlyBase ID
FBal0012759
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
Co
Key Links
Genomic Maps

Mutagen
Nature of the Allele
Progenitor genotype
Cytology
Description

In addition to the amino acid replacements, there is also a Q insertion between the Q amino acids at position 2567 and 2568.

Amino acid replacement: T1561S.

Amino acid replacement: S2257G.

Amino acid replacement: Q1865term.

Point mutation.

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

CAR

Comment:

Position of mutation on reference sequence inferred by FlyBase curator based on author statement. Mutation is an insertion of three base pairs encoding a glutamine between Q2567 and Q2568. One of two mutations in this strain.

Nucleotide change:

C3168221T

Amino acid change:

Q1865term | N-PA; Q1865term | N-PB

Reported amino acid change:

Q1865term

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. One of two mutations in this strain.

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 mutant somatic clones in the eye, almost completely lack R8 cells or other neurons.

NCo mutants exhibit thickened wing veins with deltas.

NCo mutants exhibit elevated levels of asymmetry and reduced mean character size relative to Canton-S flies for thoracic bristles.

NCo mutants show significantly reduced mean character size for orbital bristles compared to Canton-S flies.

Homozygous clones in the wing disc disrupt the dorsal/ventral boundary.

Homozygous mutant clones in the wing disc fail to respect the dorsal ventral boundary.

Thickened vein mutant.

Strong neurogenic phenotype: overproduction of adult thoracic bristles. Heterozygotes have thickened wing veins that expand to form deltas at the junction of the wing tip and overproduce thoracic microchaetae. The presence of NCo enhances the phenotype of hypomorphic and null alleles of Dl.

Semilethal when heterozygous with Nnd-3.

N68j/NCo flies are almost wild-type.

Wing tips seldom notched; veins thickened, with deltas. Acrostichal rows irregular. NCo/Nnd-3 heterozygotes lethal; rare survivors sterile and weak. NCo/+ females show thickened wing veins (a Confluens-like phenotype) more frequently than nicked or notched wings. Also, NCo heterozygous females with an extra dose of 3C6-7 <up>Dp(1;1)Co or Dp(1;2)51b</up> or hemizygous males with Dp(1;2)51b have an enhanced Confluens-like wing phenotype.

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

Phenotype is suppressed by su(N)1; NCo/su(N)1 flies have only slight thickening of wing vein L2, occasional thickening of the crossveins, but no deltas. NCo su(N)1 double homozygotes are almost completely wild type.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer

Welshons, 1955.

Comments
Comments

A N phenotype can also result from duplication of N+, e.g. Dp(1;1)Co. Relation to N illustrated by three T(1;Y)'s with breakpoints in 3C: T(1;Y)D7, T(1;Y)R38 and T(1;Y)W17. The segmental duplication formed from T(1;Y)D7 and T(1;Y)R38 is Confluens in phenotype; the corresponding deficiency is normal. The segmental deficiency formed from T(1;Y)R38 and T(1;Y)W17 is N in phenotype and the corresponding duplication is normal. In addition to T(1;Y)R38, two other translocations appear to separate Dp(1;1)Co and N : T(1;Y)R30 and T(1;Y)J100 (Merriam and colleagues).

Mapped by genetic recombination to between NAx-9 and Nnd-2.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (7)
References (26)