Based on limited published evidence, TOGARAM2 is a microtubule-associated protein involved in cilium organization and axonemal microtubule regulation. GO annotations indicate roles in cytoplasmic microtubule binding and microtubule cytoskeleton organization. Recently, TOGARAM2 was identified as a TAZ transcriptional target that promotes cell proliferation, migration, and invasion in HPV18+ cervical cancers 1. Additionally, TOGARAM2 variants have been proposed as a potential cause of autosomal recessive non-syndromic hearing loss, with protein localization to cochlear hair cells 2, suggesting roles in kinociliary function essential for hearing.