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.
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.
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: very light yellowish-pink.
Malpighian tubule colour: colourless.
Eye colour: light buff or yellowish, lighter in male.
wi has abnormal eye color phenotype, non-enhanceable by Rga03834
wi has abnormal eye color phenotype, non-suppressible by Rga03834
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
wi has phenotype, enhanceable by Ts(YSt;2Lt)B110+Ts(YSt;2Rt)R15
wi has phenotype, enhanceable by Ts(YLt;2Rt)G10+Ts(YLt;2Lt)R155
wi has phenotype, enhanceable by Ts(YSt;2Lt)L23+Ts(YSt;2Rt)R155
wi has phenotype, enhanceable by Ts(YSt;2Lt)H149+Ts(YSt;2Rt)R14
wi has phenotype, enhanceable by Dp(2;Y)J64
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-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/we(g) is an enhancer of pigment cell phenotype of g2
wi/we(g) is an enhancer of pigment cell phenotype of g50e
sgl05007, wi has pigment cell phenotype
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.
Sturtevant, 1918.
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.