TM9S1 Polyclonal Antibody, 100ul Drying & Desiccation and White)

and White)

Additional transcript variants have been describe

Mutations in this gene cause coenzyme Q10 deficiency| a mitochondrial encephalomyopathy| and also COQ2 nephropathy| an inherited form of mitochondriopathy with primary renal involvement

GO annotations related to this gene include receptor binding and ATPase activity

The encoded protein regulates signaling pathways that affect cell proliferation and adhesion

TM9S1 Polyclonal Antibody, 100ul Drying & Desiccation and White)Belongs to the nonaspanin (TM9SF) family.,tissue specificity: Expressed in lung, pancreas, kidney, liver, placenta, skeletal muscle, heart and brain. The amount in skeletal muscle, heart and brain were considerably lower than in the other tissues.,