Premature stop codon at amino acid 188.
C16324463T
Q189term | cact-PA; Q189term | cact-PB; Q189term | cact-PC; Q189term | cact-PD; Q189term | cact-PE
?188term
Reported as a premature stop codon at amino acid 188 (V). The point mutation is annotated as Q189@, since Gln to Stop is more likely than Val to Stop and the statement could be interpreted as a premature stop after codon 188.
lamellocyte (with cact7)
The ability of cactE8/cact3 larvae to encapsulate L.boulardi eggs is significantly increased compared to that of control larvae.
Lamellocytes appear in circulation during the second instar stage in cact7/cact3 larvae and are abundant in the hemolymph of third instar larvae (5-20%), where they participate in the formation of melanotic tumours. The crystal cell population is not affected. Lamellocytes are present in the lymph glands of third instar mutant larvae.
cactE8/cact3 larvae are viable at 24 and 48 hours after fertilisation. By 72 hours after fertilisation there is some lethality and delay in the rate of development compared to control siblings. Only 40% of the larvae survive to 120 hours after fertilisation, and only 4% of the larvae make white prepupae. Over 90% of larvae have melanotic capsules. Hemocyte density in cactE8/cact3 hemolymph is more than 10-fold higher than in the hemolymph of control or heterozygous larvae. There are an increased number of lamellocytes in the hemolymph compared to control larvae. The lymph glands of 5 to 8 day old animals are abnormally large and there are many more hemocytes per lobe. Heterozygous adults do not have melanotic capsules.
Embryos derived from germline clones show a strong ventralised phenotype but retain dorsoventral polarity.
Strong ventralizing phenotype: lack of all dorsally and laterally derived structures and the expansion of the ventral epidermis around the entire circumference. Expansion of twi expression in terminal regions.
cact3/cactE8 has lethal | larval stage phenotype, suppressible | partially by Adgf-Ahs.PD
cact3 has lethal | recessive phenotype, suppressible by Df(2L)TW119
cact3/cactE8 has melanotic mass phenotype | third instar larval stage phenotype, non-suppressible by Adgf-Ahs.PD
Df(2L)TW119, cact3 has viable phenotype
Tl3, cact3/cact[+] has melanotic mass phenotype phenotype
Tl10b, cact3/cact[+] has melanotic mass phenotype phenotype
Tl[+]/Tl10b, cact3 has melanotic mass phenotype phenotype
Tl[+]/Tl3, cact3 has melanotic mass phenotype phenotype
cact3/cactE8 has melanotic mass | third instar larval stage phenotype, non-suppressible by Adgf-Ahs.PD
Tl3, cact3/cact[+] has melanotic mass phenotype
Tl10b, cact3/cact[+] has melanotic mass phenotype
Tl[+]/Tl10b, cact3 has melanotic mass phenotype
Tl[+]/Tl3, cact3 has melanotic mass phenotype
The lethality associated with homozygous cact3 mutants is rescued by Df(2L)TW119, which removes Dif and dl.
cact3/cact7 is partially rescued by cactUAS.cQa/Scer\GAL4T98
cact3/cact7 is partially rescued by Scer\GAL4T59/cactUAS.cQa
cact3/cact7 is partially rescued by Scer\GAL4e33C/cactUAS.cQa
cact3/cact5 is partially rescued by cactUAS.cQa/Scer\GAL4T98
cact3/cact5 is partially rescued by Scer\GAL4T59/cactUAS.cQa
cact3/cact5 is partially rescued by Scer\GAL4e33C/cactUAS.cQa
cact3/cact5 is partially rescued by cactUAS.cQa/Scer\GAL4T100
cact3/cact7 is not rescued by cactUAS.cQa/Scer\GAL4e13C
cact3/cact5 is not rescued by cactUAS.cQa/Scer\GAL4e13C