This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLMAP-20-RE | 20 (40 μL) | 200 μL |  |
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| SLMAP-20-OR | 20 (40 μL) | 200 μL |  |
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| SLMAP-20-GO | 20 (40 μL) | 200 μL |  |
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| SLMAP-20-GR | 20 (40 μL) | 200 μL |  |
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| SLMAP-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
Gene Symbol : SLMAP
Gene Name : Sarcolemma associated protein
Chromosome : CHR 3: 577,562,20-579,300,12
Locus : 3p14.3
Alt. Genes : FEM1B
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