Automated description from the Alliance of Genome Resources (Release 5.2.2)
Predicted to enable proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in vacuolar acidification. Predicted to act upstream of or within ion transport. Located in several cellular components, including apical plasma membrane; microvillus; and ruffle. Is expressed in several structures, including genitourinary system; integumental system; limb; nervous system; and sensory organ. Used to study autosomal dominant congenital deafness with onychodystrophy. Human ortholog(s) of this gene implicated in autosomal dominant congenital deafness with onychodystrophy. Orthologous to human ATP6V1B2 (ATPase H+ transporting V1 subunit B2).