Amino acid replacement: A696V. Amino acid replacement: A703T. A703 is a highly conserved residue within the kinase II subdomain II.
C5481551T
A696V | ksr-PA; A696V | ksr-PB; A696V | ksr-PC; A696V | ksr-PD
A696V
One of two nucleotide substitutions in the ksr coding region in the allele.
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
G5481531A
A703T | ksr-PA; A703T | ksr-PB; A703T | ksr-PC; A703T | ksr-PD
A703T
One of two nucleotide substitutions in the ksr coding region in the allele. It falls within a highly conserved residue within the kinase subdomain II.
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
abdominal segment 8 & cephalopharyngeal skeleton | germ-line clone
abdominal segment 9 & cephalopharyngeal skeleton | germ-line clone
abdominal segment 10 & cephalopharyngeal skeleton | germ-line clone
abdominal segment 11 & cephalopharyngeal skeleton | germ-line clone
ksrS-638 embryos (as well as ksrS-638/ksrS-627 that show a stronger phenotype) derived from mothers bearing ksrS-638 mutant germline clones and thus lacking both maternal and zygotic ksr do not show any loss of muscle founder cells at late embryonic stages and only display rather mild visceral muscle phenotypes such as myotube stretching defects at stage 13/14 and incomplete midgut constriction at the end of embryogenesis.
ksrS-638 homozygous clones in the dorsal air sac primordium grow more slowly than wild-type clones and never contribute to the tip of the primordium.
Clonal analysis fails to produce clones of ksrS-638 suggesting ksr is required for cell proliferation or survival. Embryos derived from germline clones reveal severe terminal defects. They are missing posterior structures beyond the seventh abdominal segment and have collapsed head skeleton. Embryos derived from germline clones of ksrS-638 reveal severe terminal defects.
ksrS-638 is a suppressor of visible phenotype of C3GUAS.Tag:MYC,Tag:M(c-SRC), Scer\GAL4dpp.blk1
ksrS-638 is a suppressor of visible phenotype of C3GUAS.Tag:MYC,Tag:M(c-SRC), Scer\GAL4GMR.PF
ksrS-638 has terminalia | germline clone phenotype, suppressible by Raf::tor13D.hs.sev
ksrS-638 is a suppressor of wing vein L3 phenotype of C3GUAS.Tag:MYC,Tag:M(c-SRC), Scer\GAL4dpp.blk1
ksrS-638 is a suppressor of eye phenotype of C3GUAS.Tag:MYC,Tag:M(c-SRC), Scer\GAL4GMR.PF
ksrS-638 is a suppressor of eye phenotype of Ras85DV12.sev
ksrS-638 is a suppressor of eye phenotype of Ras85D::Src64BV12.ΔCAAX.sev
Dominantly suppresses the eye phenotype caused by C3GScer\UAS.T:Hsap\MYC,T:Ggal\Myr3 expressed under the control of Scer\GAL4GMR.PF. Completely dominantly suppresses the wing vein phenotype caused by C3GScer\UAS.T:Hsap\MYC,T:Ggal\Myr3 expressed under the control of Scer\GAL4dpp.blk1.
The terminal defect phenotype seen in germline clones of ksrS-638 can be partially rescued by the injection of mRNA generated from phl::tor13D.hs.sev. Dominantly suppresses the rough eye phenotype of Ras85DV12.sev. Suppresses the rough eye phenotype of Ras85D::Src64BV12.ΔCAAX.sev. The terminal defects of embryos derived from homozygous ksrS-638 germline clones can be partially rescued by the injection of mRNA generated from phl::tor13D.hs.sev.