viable (with mer-on-3pi9)
Shows lethality from the first to third larval instar when heterozygous with the MBT chromosome. Brain tumours are seen.
Lethal and tumour inducing over the MBT chromosome. Homozygotes die during the third larval instar. merpi9/mer14 animals are viable. Homozygotes show the formation of melanotic tumours. Gaps in somatic pairing are seen in the polytene chromosomes of heterozygous salivary glands. Heterozygotes show resistance to 1mM methyl methanesulfonate but not to 5mM hydroxyurea.
Shows strong somatic pairing defect in the salivary chromosomes. Causes significant melanotic tumor formation in larvae. Shows tumor formation when heterozygous with the MBT chromosome. Lethal when heterozygous with the MBT chromosome.
mer-on-314 is an enhancer of lethal | embryonic stage phenotype of AntpAus
mer-on-314, pll2 has lethal | pupal stage phenotype
mer-on-314, tld6 has lethal | pupal stage phenotype
Df(3R)Espl1, mer-on-314 has lethal | pupal stage phenotype
mer-on-314, neur3 has lethal | larval stage phenotype
mer-on-314, pll8 has lethal | larval stage phenotype
Df(3R)XTA1, mer-on-314 has lethal | larval stage phenotype
pll8 mer14 induces neoplasms. mer14 Df(3R)Espl1 results in anal plate neoplasms.