G17419419A
W17term | cnk-PA; W17term | cnk-PB
W17term
G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Amino acid replacement: W17term.
cnk63F/Df(2R)BSC161 embryos derived from mothers bearing cnk63F mutant germline clones and thus lacking both maternal and zygotic cnk show a complete loss of muscle founder cells at late embryonic stages. The embryos also display mild defects in the formation of ectodermal and endodermal derivatives of the alimentary tract (hindgut and Malpighian tubules are shortened) as well as severe heart and dorsal muscle formation defects, absence of eve-positive pericardial cells, impaired longitudinal visceral muscle migration, abnormal muscle attachment sites and impaired tracheal development.
cnk63F;cnkfTRG1248 rescue flies survive to adulthood but display rough eye phenotype.
cnk[+]/cnk63F is a suppressor | partially of size defective | pupal stage phenotype of Scer\GAL4elav-C155, jebUAS.cVa
The reduced pupal size characteristic for animals expressing jebScer\UAS.cVa under the control of Scer\GAL4elav-C155 is partially suppressed by combination with a single copy of cnk63F.
cnk63F is rescued by cnkfTRG01248.sfGFP-TVPTBF
cnk63F is rescued by cnkfTRG01248.sfGFP-TVPTBF
The lethality of cnk63F mutants is rescued by combination with cnkfTRG1248.