Automated description from the Alliance of Genome Resources (Release 7.1.0)
Predicted to be involved in central nervous system development. Located in mitochondrion. Is expressed in several structures, including alimentary system; heart; integumental system; nervous system; and sensory organ. Human ortholog(s) of this gene implicated in linear skin defects with multiple congenital anomalies 2. Orthologous to human COX7B (cytochrome c oxidase subunit 7B).