Description
Product Characteristics:
Aliases: ACATN antibody, ACATN_HUMAN antibody, Acetyl CoA transporter antibody, Acetyl Coenzyme A transporter antibody, Acetyl coenzyme A transporter 1 antibody, Acetyl-CoA transporter 1 antibody, Acetyl-coenzyme A transporter 1 antibody, AT 1 antibody, AT-1 antibody, AT1 antibody, Human Angiotensin II Type 1 Receptor antibody, Slc33a1 antibody, Solute carrier family 33 (acetyl CoA transporter) member 1 antibody, Solute carrier family 33 member 1 antibody, spastic paraplegia 42 (autosomal dominant) antibody, SPG42 antibody
Target Information: The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010]