In addition to the amino acid replacements, there is also a Q insertion between the Q amino acids at position 2567 and 2568.
Amino acid replacement: T1561S.
Amino acid replacement: S2257G.
Amino acid replacement: Q1865term.
Point mutation.
CAR
Position of mutation on reference sequence inferred by FlyBase curator based on author statement. Mutation is an insertion of three base pairs encoding a glutamine between Q2567 and Q2568. One of two mutations in this strain.
C3168221T
Q1865term | N-PA; Q1865term | N-PB
Q1865term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. One of two mutations in this strain.
eye & neuron | somatic clone
Homozygous mutant somatic clones in the eye, almost completely lack R8 cells or other neurons.
Homozygous clones in the wing disc disrupt the dorsal/ventral boundary.
Homozygous mutant clones in the wing disc fail to respect the dorsal ventral boundary.
Thickened vein mutant.
Semilethal when heterozygous with Nnd-3.
Wing tips seldom notched; veins thickened, with deltas. Acrostichal rows irregular. NCo/Nnd-3 heterozygotes lethal; rare survivors sterile and weak. NCo/+ females show thickened wing veins (a Confluens-like phenotype) more frequently than nicked or notched wings. Also, NCo heterozygous females with an extra dose of 3C6-7 <up>Dp(1;1)Co or Dp(1;2)51b</up> or hemizygous males with Dp(1;2)51b have an enhanced Confluens-like wing phenotype.
NCo has wing vein L2 phenotype, suppressible by su(N)1
Welshons, 1955.
A N phenotype can also result from duplication of N+, e.g. Dp(1;1)Co. Relation to N illustrated by three T(1;Y)'s with breakpoints in 3C: T(1;Y)D7, T(1;Y)R38 and T(1;Y)W17. The segmental duplication formed from T(1;Y)D7 and T(1;Y)R38 is Confluens in phenotype; the corresponding deficiency is normal. The segmental deficiency formed from T(1;Y)R38 and T(1;Y)W17 is N in phenotype and the corresponding duplication is normal. In addition to T(1;Y)R38, two other translocations appear to separate Dp(1;1)Co and N : T(1;Y)R30 and T(1;Y)J100 (Merriam and colleagues).
Mapped by genetic recombination to between NAx-9 and Nnd-2.