This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
SGCA-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
SGCA-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
SGCA-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
SGCA-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
SGCA-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]
Gene Symbol : SGCA
Gene Name : Sarcoglycan alpha
Chromosome : CHR 17: 501,655,16-501,759,31
Locus : 17q21.33
Alt. Genes : CELA3A
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