61A;61D3
61A;61D3-61D4
61A;61D3
bk1 << fwd << emc << bk2
The salivary gland distal tip does not initiate turning and migration in embryos homozygous for Df(3L)emc-E12 by stage 14.
Df(3L)emc-E12 embryos show defects in tracheal invagination.
The Df(3L)emc-E12 chromosome does not act as a dominant suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion).
Heterozygosity for Df(3L)emc-E12 results in 0.7% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
The size of the salivary gland lumen is reduced in homozygous embryos.
Wild-type clones made in the ovaries of a mutant female, are significantly larger than clones of heterozygous mutant cells. This size difference is greater in clones initiated at 48 hours after egg laying (AEL) than 2 hours AEL.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Heterozygosity for this deletion enhances the mutant ovarian phenotype of ovoD2.
Homozygotes are embryonic lethal. emc1/Df(3L)emc-E12 clones in the wing show defects in cell proliferation but overall wing size is not affected due to compensation by growth of surrounding non-mutant cells. Clones are very elongated and preferentially appear along the veins and wing margin. Clones can differentiate veins but exhibit an emc phenotype.
Deletes approximately 10 chromosomal bands, including the emc locus.
Limits of break 1 from polytene analysis (FBrf0080317) Left limit of break 2 from polytene analysis (FBrf0080317) Right limit of break 2 from polytene analysis (FBrf0085269)