This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FLCN-20-RE | 20 (40 μL) | 200 μL |  |
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| FLCN-20-OR | 20 (40 μL) | 200 μL |  |
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| FLCN-20-GO | 20 (40 μL) | 200 μL |  |
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| FLCN-20-GR | 20 (40 μL) | 200 μL |  |
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| FLCN-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Gene Symbol : FLCN
Gene Name : Folliculin
Chromosome : CHR 17: 172,371,87-172,069,44
Locus : 17p11.2
Alt. Genes : ZNF263
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