TM9S1 Polyclonal Antibody, 100ul Drying & Desiccation GO annotations related to this

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

Rho (see MIM 165390)

5-trisphosphate to 1

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

These two variants encode distinct isoforms which differ in activity and regulation

TM9S1 Polyclonal Antibody, 100ul Drying & Desiccation GO annotations related to thisBelongs 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.,