FB2024_03 , released June 25, 2024
Allele: Dmel\wi
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General Information
Symbol
Dmel\wi
Species
D. melanogaster
Name
ivory
FlyBase ID
FBal0018254
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
white-ivory
Key Links
Genomic Maps

Mutagen
Nature of the Allele
Progenitor genotype
Cytology
Description

Duplication of sequences from intron 1 to the start of exon 3.

Duplication of sequences from intron 1 to start of exon 3.

Duplication of 2.96kb within the w gene.

2.96kb internal tandem duplicated sequence.

2.9kb duplication of part of the first intron, second exon, small second intron and part of the third exon.

Duplication of intron 1 and exon 2.

Duplication of intron 1 sequences.

Duplication of a 2.9kb sequence within w.

Duplication of 2.9kb DNA.

Duplication of 2.9kb of DNA within the w locus (FBrf0037618).

Tandem duplication of 2.9kb within the w locus.

Cloning and analysis of Southern blots of wi DNA indicate the presence of a 2.9 kb duplication within the white locus (Karess and Rubin, 1982). Revertants are produced by excision of one copy of the repeat in derivatives wi+B, wi+C, wi+D and wi+E. wi+A and the partial revertant wip are insertion mutations that are more complex, their altered phenotype apparently resulting from the insertion of new DNA into wi and the loss of some wi DNA. 2.9kb duplication of intron 1 map site (kb): -0.17 to +2.80; Origin = insertion of wa copia; '-' values to left (telomere) end; '+' values to right (centromere) end.

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

This is an update from the original FlyBase annotation ( X:2792985..2795592 ), which was based on FBrf041384 and accession GB:X02974). The new coordinates are from FBrf0128658. The "insertion" in this case is a tandemly duplicated copy of the indicated region in the mutant. The sequence GCATCT is present at the start of the duplicated region and there are two tandemly repeats of GCATCT at the junction between the upstream and downstream copies of the duplicated region.

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

Homozygotes have faint pink eyes with only 0.6% red pigment (compared to 100% pigment in wild type).

Eye colour: pale yellow pink.

Eye colour: homozygous males lighter than homozygous females. Triple X metafemale individuals homozygous for wi exhibit a darker eye colour than wi homozygous XX females.

Eye colour: wsp1/wi flies have orange-brown eyes, which darken with age.

Eye colour: very light yellowish-pink.

Malpighian tubule colour: colourless.

Eye colour: light buff or yellowish, lighter in male.

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

wi has abnormal eye color phenotype, non-enhanceable by Rga03834

NOT suppressed by
Statement
Reference

wi has abnormal eye color phenotype, non-suppressible by Rga03834

Enhancer of
Statement
Reference

wi/we(g) is an enhancer of abnormal eye color phenotype of g50e

wi/we(g) is an enhancer of abnormal eye color phenotype of g2

Phenotype Manifest In
Enhanced by
Statement
Reference

wi has phenotype, enhanceable by Ufo1

wi has phenotype, enhanceable by Dp(2;Y)J64

NOT Enhanced by
Statement
Reference

wi has phenotype, non-enhanceable by Low1

wi has phenotype, non-enhanceable by Mowgamma

wi has phenotype, non-enhanceable by Wowγb

wi has phenotype, non-enhanceable by Wowγe

wi has phenotype, non-enhanceable by Wowems1

wi has phenotype, non-enhanceable by Wowhd1

wi has phenotype, non-enhanceable by In(3)Msu1

wi has phenotype, non-enhanceable by In(3)Msu2

wi has phenotype, non-enhanceable by Ts(YLt;2Lt)R14+Ts(YSt;2Rt)L110

wi has phenotype, non-enhanceable by Ts(YSt;2Rt)L107+Ts(YSt;2Lt)P59

wi has phenotype, non-enhanceable by Ts(YLt;2Rt)B202

wi has phenotype, non-enhanceable by Ts(YSt;3Rt)A31+Ts(YSt;3Lt)D228

wi has phenotype, non-enhanceable by Ts(YSt;3Lt)G48+Ts(YSt;3Rt)R36

wi has phenotype, non-enhanceable by Ts(YLt;3Lt)B116+Ts(YLt;3Rt)G48

wi has phenotype, non-enhanceable by Ts(YSt;3Rt)G73+Ts(YSt;3Lt)R128

wi has phenotype, non-enhanceable by E(wa)1

wi has phenotype, non-enhanceable by DoaHD

wi has phenotype, non-enhanceable by Doa3

wi has phenotype, non-enhanceable by Doa4

wi has phenotype, non-enhanceable by Doa5

wi has phenotype, non-enhanceable by Doa6

wi has phenotype, non-enhanceable by Doa7

wi has phenotype, non-enhanceable by Doa8

wi has phenotype, non-enhanceable by Doa9

Suppressed by
Statement
Reference

wi has phenotype, suppressible by Rm62D

wi has phenotype, suppressible by Rm62Dem

wi has phenotype, suppressible by Rm62E

wi has phenotype, suppressible by Rm62F

wi has phenotype, suppressible by Rm62H

wi has phenotype, suppressible by Rm62K

NOT suppressed by
Statement
Reference

wi has phenotype, non-suppressible by Low1

wi has phenotype, non-suppressible by Mowgamma

wi has phenotype, non-suppressible by Wowγb

wi has phenotype, non-suppressible by Wowγe

wi has phenotype, non-suppressible by Wowems1

wi has phenotype, non-suppressible by Wowhd1

wi has phenotype, non-suppressible by In(3)Msu1

wi has phenotype, non-suppressible by In(3)Msu2

wi has phenotype, non-suppressible by Ts(YLt;2Rt)B110+Ts(YSt;2Lt)D20

wi has phenotype, non-suppressible by Ts(YLt;2Lt)R14+Ts(YSt;2Rt)L110

wi has phenotype, non-suppressible by Ts(YSt;2Rt)L107+Ts(YSt;2Lt)P59

wi has phenotype, non-suppressible by Ts(YLt;2Rt)B202

wi has phenotype, non-suppressible by Ts(YSt;3Rt)A31+Ts(YSt;3Lt)D228

wi has phenotype, non-suppressible by Ts(YSt;3Lt)G48+Ts(YSt;3Rt)R36

wi has phenotype, non-suppressible by Ts(YLt;3Lt)B116+Ts(YLt;3Rt)G48

wi has phenotype, non-suppressible by Ts(YSt;3Rt)G73+Ts(YSt;3Lt)R128

wi has phenotype, non-suppressible by Pcf11γb

wi has phenotype, non-suppressible by Pcf11γc

wi has phenotype, non-suppressible by Pcf11γd

wi has phenotype, non-suppressible by Pcf11EMS3

wi has phenotype, non-suppressible by Pcf11EMS4

wi has phenotype, non-suppressible by Pcf11EMS5

wi has phenotype, non-suppressible by Pcf11hd1

wi has phenotype, non-suppressible by Pcf11γsc

wi has phenotype, non-suppressible by DoaHD

wi has phenotype, non-suppressible by Doa3

wi has phenotype, non-suppressible by Doa4

wi has phenotype, non-suppressible by Doa5

wi has phenotype, non-suppressible by Doa6

wi has phenotype, non-suppressible by Doa7

wi has phenotype, non-suppressible by Doa8

wi has phenotype, non-suppressible by Doa9

wi has phenotype, non-suppressible by su(Hw)2

Enhancer of
Statement
Reference

wi/we(g) is an enhancer of pigment cell phenotype of g2

wi/we(g) is an enhancer of pigment cell phenotype of g50e

Other
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

Flies with a wi/we(g) mutant genotype enhance the eye colour defective phenotype of g2 and g50e homozygous mutants leading to a greater reduction of red pigment in the eye. Male wi, g53d double mutant flies have lower levels of pigment in the eye than wi single mutants, leading to a change in eye colour from faint pink to completely white.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Complements
Comments

Complementation of wsp1 only with age.

Images (2)
Stocks (13)
Notes on Origin
Discoverer

Sturtevant, 1918.

Comments
Comments

Not dosage compensated.

Unstable, reverting spontaneously to w+ with a frequency of 5 x 10-5 in wi/wi females and 5 x 10-6 in wi/Y males. Frequency of somatic reversion increased by X irradiation of young larvae.

wi females heterozygous for a w- deletion revert at a frequency of 0.25 x 10-5. Frequency of germinal reversions increased by X rays.

Recombination between flanking w alleles reduced in wi, but restored in its revertants.

The allele is modestly unstable. Reverts to wild type at a frequency of 5 x 10-5 in homozygous females, and 5x 10-6 in males and deletion heterozygous females.

mle4 has no effect on the dosage compensation of we, wapl, wF4-2, wa2, Dp(1;1)w+61e19 or wi.

Moderately unstable allele. Wild type revertants of this mutation recovered by chemical mutagens is achieved by a deletion of the 2.96kb tandemly duplicated sequences.

Seven carcinogenic compounds have been tested using a wi reversion assay.

Placed on the genetic map distal to w1.

External Crossreferences and Linkouts ( 2 )
Crossreferences
GenBank Nucleotide - A collection of sequences from several sources, including GenBank, RefSeq, TPA, and PDB.
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
wi
Secondary FlyBase IDs
    References (59)