Nadk2^m1Jcs

The phenotypic deviant was identified by by hindlimb wasting, gait abnormalities, and shakiness following multidose ethylnitrosourea (ENU) treatments. Sequence analysis indicates that this recessive mutation is a C to T substitution at position 977 resulting in a serine to leucine substitution (S326L) in exon 10. (J:332444)