FLCN 抗体
(Folliculin (FLCN))
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].
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Latest Publications for our FLCN 抗体
: "Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stability." in: Human mutation, Vol. 32, Issue 8, pp. 921-9, (2011) (PubMed).Aliases for FLCN 抗体
folliculin (FLCN) 抗体folliculin (flcn) 抗体
folliculin S homeolog (flcn.S) 抗体
folliculin (Flcn) 抗体
AU014660 抗体
B430214A04Rik 抗体
Bhd 抗体
BHD 抗体
FLCL 抗体
FLCN 抗体
flcn 抗体
wu:fe38g11 抗体
zgc:136982 抗体
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