CRISPR/Cas9 technology generated a CCA to CTA change at residue 89 resulting in an amino acid substitution from proline to leucine. Western blot analysis confirmed expression of the protein, with a 30% reduction on the mutant protein expression in heterozygotes and 60% reduction in homozygotes. The P89L mutation recapitulates mutations found in two brothers with autism spectrum disorder. (J:247060)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count