Amino acid replacement: D681N.
The D681N mutation is within the second 'MAM' domain.
G16632392A
D681N | Alk-PA; D681N | Alk-PB
D681N
Site of nucleic acid difference inferred by FlyBase based on reported amino acid change
Induced on: P{neoFRT}42D chromosome.
Selected as: a mutant that fails to complement the Df(2R)Alk-21 deficiency.