CRISPR/cas9 genome editing generated an indel mutation with a single T nucleotide insertion within exon 3. The indel introduces an early stop codon and results in a null allele. (J:334328)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count