Mutation in the splice donor site at the 3' end of exon 5, resulting in a premature stop codon.
G27146884A
G?A
Mutation in the splice donor at the end of exon 5.
In embryos derived from vtdγ26-6 females and undergoing mitosis 13, there is an increase in the number of nuclei showing the loose alignment of chromosomes seen at the metaphase to anaphase transition, and the chromosomes appear to be less condensed than normal. No mitotic abnormalities are seen in these embryos before mitosis 11, and the embryos subsequently achieve normal metaphase figures with proper condensation and alignment.
Imaginal discs are not evident in vtd80Fh-35/vtdγ26-6 third instar larvae.
Metaphase chromosome spreads of vtd80Fh-35/vtdγ26-6 third larval instar neuroblasts consist of individual sister chromatids that are not conjoined at the centromere. In addition, the chromosome complements are often aneuploid.
vtdγ26-6/vtd[+] is an enhancer of scutellar bristle phenotype of Nspl-1
Df(3L)K-2/vtdγ26-6 is rescued by vtdUAS.Tag:HA/Scer\GAL4Act5C.PI