Splice acceptor mutation of CAG to CAA, in the extracellular domain.
G5221401A
Position of mutation on reference sequence inferred by FlyBase curator based on author statement. Splice acceptor mutation of CAG to CAA, affecting C75 and K76 (figure 1).
Clones within an adult wing that intersects the margin causes formation of triple row in an area that normally produces dorsal row.
Homozygotes display weak head defects, wrinkled dorsal epidermis and internalised and often disorganised filzkorper. Lethal when heterozygous with tkv4, tkv5, tkv7 and tkv8, but not with Df(2L)tkv2. Female transheterozygotes with Df(2L)tkv2 are viable and display a wing phenotype, wing veins are very thick and short along the proximal distal axis, transheterozygotes with Df(2L)tkv3 display wing veins that are very thick and short along the proximal distal axis. Adult Df(2L)tkv3/tkv6 and tkv1/tkv6 females lay eggs, some of the embryos from these females crossed to wild type males die showing a weakly ventralised phenotype.
Viable with strong tkv phenotype over Tp(2;3)tkv (Szidonya and Reuter, 1988). homozygous lethal; hemizygous viable with thick veins;
gbbD4, tkv6 has lethal | recessive | embryonic stage phenotype
gbbD8, tkv6 has lethal | recessive | embryonic stage phenotype
E(tkv)D1D1, tkv6 has visible | recessive phenotype
E(tkv)D2D2, tkv6 has visible | recessive phenotype
E(tkv)D2D2, tkv6 has visible | dominant phenotype
E(tkv)D1D1, tkv6 has visible | dominant phenotype
tkv6 is an enhancer of embryonic midgut constriction phenotype of gbbD8/gbbD4
gbbD4, tkv6 has tarsal segment phenotype
shn1, tkv6 has tarsal segment phenotype
E(tkv)D1D1, tkv6 has scutum phenotype
E(tkv)D2D2, tkv6 has scutum phenotype
gbbD8/gbbD4, tkv6 has embryonic/first instar larval cuticle phenotype
gbbD8/gbbD4, tkv6 has embryonic head phenotype
E(tkv)D2D2, tkv6 has mesothoracic bristle phenotype
E(tkv)D1D1, tkv6 has mesothoracic bristle phenotype
shn1 dominantly enhances the wing vein defects of tkv6 flies, and also produces defects in proximal/distal patterning of the leg in these flies; distal elements such as claws and distal tarsal segments are deleted in tkv6 shn1; tkv6 flies. The phenotype is dominantly enhanced by E(tkv)D1D1 or E(tkv)D2D2; tkv6 flies carrying one copy of E(tkv)D1D1 or E(tkv)D2D2 have defects in the notum. The phenotype is dominantly enhanced by MadD3, MadD14, MadD15, MadD16, MadD24, gbbD4, gbbD8, gbbD20, MedD5, putD13 or putD18; tkv6 flies carrying one copy of MadD3, MadD14, MadD15, MadD16, MadD24, gbbD4, gbbD8, gbbD20, MedD5, putD13 or putD18 have defects in the notum and legs. No interaction with dpps5, shn1, sax5, MadP1, MadP1 or put135 is seen in double heterozygous flies. tkv6 gbbD4/tkv6 gbbD8 embryos form only one midgut constriction. gbbD4/tkv6 gbbD8 embryos have head defects and an excessive ventral curvature. gbbD4/tkv6 gbbD8 embryos derived from homozygous tkv6 females have a dorsal open phenotype.
Szidonya.