Your search for "flcn" returned 138 TaqMan® SNP Genotyping Assays
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]
AU014660, B430214A04RIK, BHD, FLCL, FLCN
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