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disease:Defects in MT-ND3 are a cause of complex I mitochondrial respiratory chain deficiency

CACNG1 is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members that function as transmembrane AMPA receptor regulatory proteins (TARPs)

CPT I is the key enzyme in the carnitine-dependent transport across the mitochondrial inner membrane and its deficiency results in a decreased rate of fatty acid beta-oxidation

UBQLN3 is specifically expressed in the testis

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