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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC33A1-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| SLC33A1-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| SLC33A1-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| SLC33A1-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| SLC33A1-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
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]
Gene Symbol : SLC33A1
Gene Name : Solute carrier family 33 member 1
Chromosome : CHR 3: 155,854,458-155,826,510
Locus : 3q25.31
Alt. Genes : FEM1B
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.