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Reviewed November 2012

What is the official name of the FLCN gene?

The official name of this gene is “folliculin.”

FLCN is the gene's official symbol. The FLCN gene is also known by other names, listed below.

Read more about gene names and symbols on the About page.

What is the normal function of the FLCN gene?

The FLCN gene provides instructions for making a protein called folliculin. Researchers have not determined the protein's function, but they believe it may act as a tumor suppressor. Tumor suppressors help control the growth and division of cells.

The folliculin protein is present in many of the body's tissues, including the brain, heart, placenta, testis, skin, lung, and kidney. Researchers have proposed several possible roles for the protein within cells. Folliculin may be important for cells' uptake of foreign particles (endocytosis or phagocytosis). The protein may also play a role in the structural framework that helps to define the shape, size, and movement of a cell (the cytoskeleton) and in interactions between cells. In the lung, it is thought that folliculin plays a role in repairing and re-forming lung tissue following damage.

How are changes in the FLCN gene related to health conditions?

Birt-Hogg-Dubé syndrome - caused by mutations in the FLCN gene

Several mutations in the FLCN gene have been identified in people with Birt-Hogg-Dubé syndrome, a condition characterized by multiple noncancerous (benign) skin tumors, an increased risk of other tumors, and lung cysts. Most of these mutations insert or delete one or more protein building blocks (amino acids) in the folliculin protein. These mutations lead to the production of an abnormally small, nonfunctional version of this protein. Without folliculin, researchers believe that cells can grow and divide uncontrollably to form cancerous or noncancerous tumors. They have not determined how a loss of folliculin increases the risk of lung abnormalities that are often associated with Birt-Hogg-Dubé syndrome.

primary spontaneous pneumothorax - caused by mutations in the FLCN gene

At least eight mutations in the FLCN gene have been found to cause primary spontaneous pneumothorax. This condition occurs when air builds up abnormally in the space between the lungs and the chest cavity (plural space), potentially leading to a partial or complete collapse of the lung. Many of these mutations result in the production of a folliculin protein that is abnormally short and nonfunctional. Researchers have not determined how FLCN gene mutations lead to the development of primary spontaneous pneumothorax. One theory is that the altered folliculin protein may trigger inflammation within lung tissue that could lead to the formation of small sacs of air (blebs) in the tissue. These blebs can rupture, causing air to leak into the pleural space. People who have an FLCN gene mutation associated with primary spontaneous pneumothorax all appear to develop blebs, but it is estimated that only 40 percent of those individuals go on to have a primary spontaneous pneumothorax.

other cancers - associated with the FLCN gene

Some gene mutations are acquired during a person's lifetime and are present only in certain cells. These changes, called somatic mutations, are not inherited. Somatic mutations in the FLCN gene are probably associated with several types of nonhereditary (sporadic) tumors. Specifically, somatic FLCN mutations have been identified in some cases of clear cell renal cell carcinoma (a type of kidney cancer) and in some colon cancers. These mutations may change the structure of the folliculin protein, disrupting its tumor suppressor function. Researchers do not know how FLCN mutations lead to these particular forms of cancer.

Where is the FLCN gene located?

Cytogenetic Location: 17p11.2

Molecular Location on chromosome 17: base pairs 17,206,924 to 17,237,188

(Homo sapiens Annotation Release 107, GRCh38.p2) (NCBIThis link leads to a site outside Genetics Home Reference.)

The FLCN gene is located on the short (p) arm of chromosome 17 at position 11.2.

The FLCN gene is located on the short (p) arm of chromosome 17 at position 11.2.

More precisely, the FLCN gene is located from base pair 17,206,924 to base pair 17,237,188 on chromosome 17.

See How do geneticists indicate the location of a gene? in the Handbook.

Where can I find additional information about FLCN?

You and your healthcare professional may find the following resources about FLCN helpful.

You may also be interested in these resources, which are designed for genetics professionals and researchers.

What other names do people use for the FLCN gene or gene products?

  • BHD
  • FLCL
  • MGC17998
  • MGC23445

Where can I find general information about genes?

The Handbook provides basic information about genetics in clear language.

These links provide additional genetics resources that may be useful.

What glossary definitions help with understanding FLCN?

acids ; benign ; cancer ; carcinoma ; cell ; colon ; cysts ; cytoskeleton ; endocytosis ; gene ; inflammation ; inherited ; kidney ; mutation ; phagocytosis ; placenta ; pneumothorax ; protein ; renal ; rupture ; spontaneous ; sporadic ; syndrome ; testis ; tissue ; tumor

You may find definitions for these and many other terms in the Genetics Home Reference Glossary.

See also Understanding Medical Terminology.

References (11 links)


The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? in the Handbook.

Reviewed: November 2012
Published: February 8, 2016