Otoancorin is found in the cochlea, utricule, saccule, and under the cupulae on the surface of apical dells in the sensory epithelia.[6]
In humans the gene that encodes otoancorin is called OTOA. It is on chromosome 16p12.2 and contains 28 exons. A recessive mutation in this gene called IVS12+2T>C results in deafness. The human protein has 1,153 amino acids.[6]
^Weddell T, Legan PK, Lukashkina VA, Goodyear RJ, Welstead L, Petit C, et al. (2011). "Otoancorin Knockout Mice Reveal Inertia is the Force for Hearing". American Institute of Physics Conference Series. AIP Conference Proceedings. 1403 (1): 139–140. Bibcode:2011AIPC.1403..139W. doi:10.1063/1.3658074.