A point mutation (H698D, corresponding to human disease-associated residue H662) is introduced into endogenous Sf3b1.
Amino acid replacement: H698D.
CAC570719GAT
CAC?GAT
H698D | Sf3b1-PA; H698D | Sf3b1-PB
H698D
Analogous mutation in human SF3B1 is associated with cancer.
Disease model in flies has not been developed.