Automated description from the Alliance of Genome Resources (Release 7.3.0)
Predicted to be involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Is expressed in limb long bone; otic capsule; thoracic segment skeleton; and viscerocranium. Human ortholog(s) of this gene implicated in linear skin defects with multiple congenital anomalies 3 and nuclear type mitochondrial complex I deficiency 30. Orthologous to human NDUFB11 (NADH:ubiquinone oxidoreductase subunit B11).
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