Predicted to enable catechol O-methyltransferase activity. Predicted to be involved in several processes, including auditory receptor cell development; catecholamine metabolic process; and positive regulation of protein import. Predicted to be located in apical part of cell and endoplasmic reticulum. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 63. Orthologous to human LRTOMT (leucine rich transmembrane and O-methyltransferase domain containing). [provided by Alliance of Genome Resources, Apr 2022]