FLCN
gene productBHD, DENND8B, MGC17998, MGC23445
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]
Featured antibodies
 Biorbyt |
 orb39348 |
0 references | Polyclonal |
WB
IHC
FC
|
 Atlas Antibodies |
HPA028760 |
0 references | Polyclonal |
ICC
IHC
|
Antibodies
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Supportive data in Antibodypedia
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Eligible for validation within AVI