Automated description from the Alliance of Genome Resources (Release 7.4.0)
Enables mRNA binding activity and mitochondrial ribosome binding activity. Involved in cytosolic ribosome assembly and positive regulation of mitochondrial translation. Located in mitochondrion. Is expressed in several structures, including brain ventricular layer; genitourinary system; gut; orbito-sphenoid; and tooth. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 33. Orthologous to human C1QBP (complement C1q binding protein).
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