Answer :
B. There is no lethal phenotype associated with a null mutation in the gene.
SYNTHASE ATP
Two functional domains make up the human mitochondrial ATP synthase, or complex V: F1, which is found in the mitochondrial matrix, and Fo, which is found in the inner mitochondrial membrane. Complex V phosphorylates ADP to ATP using the energy produced by the proton electrochemical gradient. The architecture, operation, and assembly of complicated V are all covered in this review. It is explained how complex V di- and oligomerization affects mitochondrial morphology. Last but not least, current treatment approaches and pathology associated with complex V deficiency are discussed. There are still unanswered concerns surrounding the structure of subunits, the molecular basis of the rotary nanomotor function, and the construction of the human complex V despite the enormous advancements made in this field of study over the last few decades. The identification of further nuclear genetic abnormalities will direct physio(patho) logical research and open the door to potential treatment approaches in the future.
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