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Diaz-Horta et al. (1) report the characterization of FAM65B (family with sequence similarity 65, member B), including its mutation in families with recessive hearing loss, its expression and localization in hair cell stereocilia, and the sensorineural hearing loss in a FAM65B knockout zebrafish model. The authors also provide a structural model of the N-terminal 300 amino acids of this 1,068 amino acid protein. This model suggests a homology to the sorting nexin (SNX) family members possessing phox homology (PX) and bin/amphiphysin/rvs (BAR) domains, which promote membrane binding and remodeling, respectively (2, 3). However, our analyses of the FAM65B sequence indicate it …

Little evidence that FAM65B belongs to the family of phox homology (PX) and bin/amphiphysin/rvs (BAR) domain-containing proteins