29C1-29C2;30C8-30C9;30D1-30D2;31A1-31A2
2Lt - 29C1 | 30C9 - 30D1 | 31A1 - 30D2 | 31A2 - 2Rt
29C1--2;[]
29C1-29C2;30C8-30C9;30D1-30D2;31A1-31A2
29C1-29C2;30C8-30C9
bk1 << fy << grk << bk2
This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).
Breakpoint 1 was mapped to a BamHI-HindIII restriction fragment. The position of the restriction fragment on the reference sequence was inferred by a FlyBase curator.
Breakpoint 1 was mapped to an EcoRI-EcoRI restriction fragment. The position of the restriction fragment on the reference sequence was inferred by a FlyBase curator.
Lethal in combination with T(Y;2)fy4.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Little if any macrophage migration occurs in homozygous embryos, with most macrophages remaining in the anterior region, clustered around the foregut, at stage 13-15.
Heterozygosity for Df(2L)N22-14 results in 1.5% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Heterozygotes show a quantitative effect on wing shape in intervein region C compared to wild type.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
The stock contains a second-site deletion uncovering l(2)gl.
The Df(2L)N22-14 chromosome acts as a dominant weak 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), but this is assumed to be a false positive result (the suppressor may not be within the bounds of the deficient region) because the 2L TAS array on the chromosome is reduced (as assayed by in situ hybridization) and it has previously been shown (FBrf0137248, FBrf0158986) that partial or complete deficiency of the 2L TAS array on the homologue suppresses silencing of brown-red variants of P{3'WP-2,wvar}2Lt.
Deletes in a proximal direction from stated breakpoint. Cytology of second break not reported.
The left Df(2L)N22-14 breakpoint lies in CG13386 or CG31898 or in the region between them, and lies in the range 2L:8399332..8401129 (R5) (predicted cytology: 29C1).
The right Df(2L)N22-14 breakpoint lies within CG13123 or nAcRα-30D or the region between them, and lies in the range 2L:9792596..9806483 (R5) (predicted cytology: 30D1).
Limits of break 1 from polytene analysis (FBrf0065509) Limits of break 2 from polytene analysis (FBrf0089969) Limits of break 3 from polytene analysis (FBrf0089969) Limits of break 4 from polytene analysis (FBrf0089969)