Name

FLCN Gene

folliculin

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]

flcn Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term flcn in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

FLCN Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for FLCN from the Pathway Commons Protein-Protein Interactions dataset.

flcnnull Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term flcnnull in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

flcnfnip Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term flcnfnip in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

flcnp0071 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term flcnp0071 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

BL8783 (FLCN) Gene Set

From NURSA Protein Complexes

proteins in the BL8783 (FLCN) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.