A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF.

BACKGROUND

Over 200 pathogenic variants in the OTOF gene encoding otoferlin are associated with sensorineural hearing loss (SNHL) and auditory neuropathy spectrum disorders (ANSD).

RESULTS

A novel splice variant, OTOF c.898-18G > A, was detected in seven Jewish Moroccan families with both SNHL and ANSD in an Israeli multicenter study. The effect on splicing was confirmed by a minigene assay, which demonstrated skipping of exon 10. This variant is absent in gnomAD and in all Jewish ethnic groups except for Moroccan Jews, with a carrier rate of 1.5% in this ancestry, suggesting a founder effect.

CONCLUSIONS

The OTOF variant represents a second founder allele associated with hearing loss in the Moroccan Jewish community and may serve as a candidate for gene therapy.