Allele-level data and p-values for non-complementation of <i>nmf9</i> by CRISPR-induced mutations.

Frequency with which animals of the indicated genotype were called abnormal by a trained observer blind to genotype is indicated for each test and allele combination, as is the average number of the five tests for which a given genotype was considered abnormal. P-values are for the one-sided Fisher’s Exact Test of the null hypothesis that mutant/nmf9 heterozygotes are not more often affected than mutant/+ heterozygotes, based on sums across all five induced alleles.
Allele-level data and p-values for non-complementation of nmf9 by CRISPR-induced mutations.