This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FRAS1-20-RE | 20 (40 μL) | 200 μL |  |
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| FRAS1-20-OR | 20 (40 μL) | 200 μL |  |
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| FRAS1-20-GO | 20 (40 μL) | 200 μL |  |
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| FRAS1-20-GR | 20 (40 μL) | 200 μL |  |
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| FRAS1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Gene Symbol : FRAS1
Gene Name : Fraser extracellular matrix complex subunit 1
Chromosome : CHR 4: 780,573,22-785,442,68
Locus : 4q21.21
Alt. Genes : KIF20A
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