Dnah5^b2b2925Clo

This ENU-induced mutation was isolated in a screen at the University of Pittsburgh. The molecular lesion is a T to A substitution at nucleotide +2 after coding nucleotide 2259 (c.2259+2T>A, NM_133365) in intron 15. This changes splice donor site G-GT to G-GA (which is assumed to be inactive). (J:175213)