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Reviewed May 2013

What is the official name of the ABCG5 gene?

The official name of this gene is “ATP binding cassette subfamily G member 5.”

ABCG5 is the gene's official symbol. The ABCG5 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 ABCG5 gene?

The ABCG5 gene provides instructions for making sterolin-1, which makes up half of a protein called sterolin. The other half of the sterolin protein, sterolin-2, is produced from a gene called ABCG8. Sterolin is involved in eliminating plant sterols, which are fatty components of plant-based foods that cannot be used by human cells.

Sterolin is a transporter protein, which is a type of protein that moves substances across cell membranes. It is found mostly in cells of the intestines and liver and transports plant sterols. After plant sterols are absorbed from food into intestinal cells, the sterolin transporters in these cells pump them back into the intestinal tract. Sterolin transporters in liver cells pump the plant sterols into a fluid called bile that is released into the intestine. From the intestine, the plant sterols are eliminated with the feces. This process removes most of the dietary plant sterols, and allows only about 5 percent of these substances to get into the bloodstream. Sterolin also helps regulate levels of cholesterol, another fatty substance found in animal products, in a similar fashion; normally about 50 percent of cholesterol in the diet is absorbed by the body.

Does the ABCG5 gene share characteristics with other genes?

The ABCG5 gene belongs to a family of genes called ABC (ATP-binding cassette transporters).

A gene family is a group of genes that share important characteristics. Classifying individual genes into families helps researchers describe how genes are related to each other. For more information, see What are gene families? in the Handbook.

How are changes in the ABCG5 gene related to health conditions?

sitosterolemia - caused by mutations in the ABCG5 gene

At least 24 ABCG5 gene mutations have been identified in people with sitosterolemia, which is a condition caused by accumulation of plant sterols. The mutations result in a defective sterolin transporter and impair the elimination of plant sterols and, to a lesser degree, cholesterol from the body. These fatty substances build up in the arteries, skin, and other tissues, resulting in clogged blood vessels that can impair blood flow (atherosclerosis), fatty skin growths (xanthomas), and the additional signs and symptoms of sitosterolemia. Excess plant sterols in red blood cells likely make their cell membranes stiff and prone to rupture, leading to a reduced number of red blood cells (anemia). Changes in the lipid composition of the membranes of red blood cells and platelets may account for the other blood abnormalities that sometimes occur in sitosterolemia.

other disorders - increased risk from variations of the ABCG5 gene

Certain normal variations (polymorphisms) in the ABCG5 gene are associated with an increased risk of gallstones, which are small pebble-like deposits in the gallbladder or the bile ducts. Bile ducts carry bile (a fluid that helps digest fats) from the liver, where bile is produced, to the gallbladder, where it is stored, and to the small intestine, where it aids in digestion. Researchers suggest that the ABCG5 gene changes that increase the risk of gallstones may result in a sterolin transporter protein that pumps more cholesterol than usual into bile. This leads to the presence of more cholesterol than can be dissolved in the bile fluid in the bile ducts and gallbladder, resulting in the formation of gallstones.

Where is the ABCG5 gene located?

Cytogenetic Location: 2p21

Molecular Location on chromosome 2: base pairs 43,806,155 to 43,838,865

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

The ABCG5 gene is located on the short (p) arm of chromosome 2 at position 21.

The ABCG5 gene is located on the short (p) arm of chromosome 2 at position 21.

More precisely, the ABCG5 gene is located from base pair 43,806,155 to base pair 43,838,865 on chromosome 2.

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

Where can I find additional information about ABCG5?

You and your healthcare professional may find the following resources about ABCG5 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 ABCG5 gene or gene products?

  • ATP-binding cassette, subfamily G, member 5
  • ATP-binding cassette sub-family G member 5
  • ATP-binding cassette, sub-family G (WHITE), member 5
  • sterolin 1
  • sterolin-1
  • STSL

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 ABCG5?

anemia ; arteries ; atherosclerosis ; ATP ; bile ; cell ; cholesterol ; digestion ; feces ; gallbladder ; gene ; intestine ; lipid ; platelets ; protein ; rupture ; sterols

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

See also Understanding Medical Terminology.

References (13 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: May 2013
Published: February 1, 2016