Amino acid replacement: M487H. Nucleotide substitution: T1460A.
The mutation falls in the C2 domain of the tld protein.
Amino acid replacement: M487K.
T24751597A
T?A
M497K | tld-PA
M487K
Position of mutation on reference sequence inferred by FlyBase curator. Difference beteween actual and reported amino acid substitution due to authors using M11 as the start Met.
T24751597A
T1460A
M497K | tld-PA
M487K
Position of mutation on reference sequence inferred by FlyBase curator. Difference beteween actual and reported amino acid substitution due to authors using M11 as the start Met.
ommatidium (with tldMBT)
tldMBT/tld1 hybrids have rough eyes at the permissive temperature. At the restrictive temperature, 30% die as pupae. The optic lobes are not hyperplastic, brain cells are differentiated but do not adhere. Pupal lethal when heterozygous with the MBT chromosome. Ubiquitous neoplasm/melanomes are seen.
Antagonistic activity towards dpp.
Weak ventralization.
Weak ventralised phenotype. Defective movements of the germ band: due to loss of the amnioserosa and because the dorsalmost cells have acquired the lateral fate of the dorsal ectoderm. Dorsal cell fates are deleted and ventrolateral mitotic domains are expanded.
weak embryonic lethal Partially ventralized. Cephalic furrow shifted dorsally; defects in germband extension. Denticle belts extended laterally.
Weak phenotype can be completely suppressed by a duplication of dpp+.
Very weak tld allele.
Weak, incompletely penetrant tld allele. Allelic series for tld antagonistic effect on dpp : tldB3 > tld14 = tld6 > tld1 > tld6P41 > tld9Q19.