Polytene chromosomes normal.
Nucleotide substitution: AA1639GC. Amino acid replacement: K355S. Nucleotide substitution: C2715A. Amino acid replacement: T714N. These mutations are in the extracellular domain of the protein.
AAA26838799AGC
AA1639GC
T356P | Tl-PB; T356P | Tl-PC; T356P | Tl-PD
K355S
The reported Lys to Ser amino acid change (AAA to AGC) requires nucleotide changes at two positions of the codon. This is one of two amino acid substitutions in Tl in this strain. The site of the nucleotide substitution in the mutant was inferred by FlyBase based on the reported amino acid change.
C26839994A
C2715A
T714N | Tl-PB; T714N | Tl-PC; T714N | Tl-PD
T714N
One of two amino acid substitutions in this strain.
increased mortality (with Tlr3)
The entire dorso-ventral axis forms neuroectoderm in homozygous Tlr4 embryos.
Cell intercalation in lateralized Tl mutant embryos proceeds normally during germ band extension.
Unique lateralized pattern. Cuticular phenotype of embryos resemble that of Toll-dominant embryos, but denticles finer and less heavily pigmented and body shape often an elongated tube. Recessive.
Dorsalized phenotype facilitates removal of perivitelline fluid.
Lateralized embryos: cuticle is an elongated tube covered with rings of denticles. dpp, zen and twi are only expressed at the poles, only transient expression of sna is seen.
Embryos from homozygous females are lateralised.
Females produced lateralized embryos.
Tl[+]/Tlr4 is an enhancer of embryonic ventral epidermis | non-rescuable maternal effect | germline clone phenotype of wekEX14
Tl[+]/Tlr4 is an enhancer of embryonic/first instar larval cuticle | ventral | non-rescuable maternal effect | germline clone phenotype of wekEX14
T. Rice.
It is not known whether one or both amino acid replacements generate the mutant phenotype. Phenotypic and molecular analysis suggests that the allele previously termed "Tlrm10" is the same mutagenic event as "Tlrm9".