Deletion.
Large deletion.
The number of corpora cardiaca cells is increased in mutant stage 17 embryos compared to wild type.
Additional neuroblasts are found in each position where the S1 neuroblasts normally form in mutant embryos.
The number of cells in the nau-expressing muscle precursor clusters is increased compared to wild-type in homozygous embryos and in homozygous embryos derived from homozygous female germline clones (lacking both maternal and zygotic function).
E(spl)rv1 shows severe neural hypertrophy, a 6--9 fold increase in nau expressing cells per cluster relative to wild type. The clusters enlarge so much that they merge to form superclusters across the midline.
Extreme embryonic neurogenic phenotype. Only remaining epidermis is indicated by a patch of cuticle in which a posterior spiracle and the remains of the pharynx are evident.
E(spl)m8-HLHrv1/E(spl)m8-HLH[+] is an enhancer of visible phenotype of Scer\GAL4Tub.PU, cswN308D.UASp
E(spl)m8-HLHrv1 is a suppressor of short lived phenotype of Hsap\TARDBPUAS.cHa, Scer\GAL4Toll-6-D42
E(spl)m8-HLHrv1/E(spl)m8-HLH[+] is an enhancer of wing vein | ectopic phenotype of Scer\GAL4Tub.PU, cswN308D.UASp
E(spl)rv1 SoxNGA1192 double mutant embryos show a combination of the neurogenic E(spl)rv1 phenotype and the anti-neural SoxNGA1192 phenotype. The neurogenic phenotype is apparent in the ventral column of the S1 neuroblasts. In the lateral column, the anti-neural phenotype of SoxNGA1192 remains unchanged in the double mutant embryos.
E(spl)rv1 grounspecified Egfrt1/Egfrf11 and E(spl)rv1 grounspecified EgfrE3/EgfrE3 flies show a simple additive phenotype.
Revertant.
Identification: Isolated by X-ray mutagenesis of E(spl)1 followed by screening for loss of ability to enhance Nspl-1.