ENU-induced C to T transition at base pair 19,957,218 (v38) on chromosome 16, or base pair 25,832 in the GenBank genomic region NC_000082 encoding Klhl6. The mutation corresponds to residue 635 in the mRNA sequence NM_183390 within exon 3 of 7 total exons. The mutation results in substitution of glutamine 197 for a premature stop codon (Q197*) in the KLHL6 protein.