S2546 Rabbit Polyclonal Antibody, 100ul Serum Mutations in this gene have

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly

20-lyase activities and is a key enzyme in the steroidogenic pathway that produces progestins

each encoding a distinct carboxyl terminus

Aberrant expression of this gene is associated with intestinal inflammation and tumorigenesis

developmental stage:Expressed in early stage of myeloid and erythroid differentiation

S2546 Rabbit Polyclonal Antibody, 100ul Serum Mutations in this gene haveThis gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy.