Skip Navigation
Genetics Home Reference: your guide to understanding genetic conditions About   Site Map   Contact Us
 
Home A service of the U.S. National Library of Medicine®
 
 
Printer-friendly version
MSTN

MSTN

Reviewed December 2008

What is the official name of the MSTN gene?

The official name of this gene is “myostatin.”

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

The MSTN gene provides instructions for making a protein called myostatin. This protein is part of the transforming growth factor beta (TGFβ) superfamily, which is a group of proteins that help control the growth and development of tissues throughout the body. Myostatin is found almost exclusively in muscles used for movement (skeletal muscles), where it is active both before and after birth. This protein normally restrains muscle growth, ensuring that muscles do not grow too large. Myostatin has been studied extensively in mice, cows, and other animals, and it appears to have a similar function in humans.

Researchers are studying myostatin as a potential treatment for various muscular dystrophies that cause muscle weakness and wasting (atrophy).

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

myostatin-related muscle hypertrophy - caused by mutations in the MSTN gene

At least one mutation in the MSTN gene has been found to cause myostatin-related muscle hypertrophy, a rare condition characterized by increased muscle mass and strength. The mutation, which is written as IVS1+5G>A, disrupts the way the gene's instructions are used to make myostatin. As a result, cells produce little or no functional myostatin. A loss of this protein in muscle cells leads to an overgrowth of muscle tissue. It does not appear to cause any other medical problems in affected individuals.

Where is the MSTN gene located?

Cytogenetic Location: 2q32.2

Molecular Location on chromosome 2: base pairs 190,055,699 to 190,062,728

The MSTN gene is located on the long (q) arm of chromosome 2 at position 32.2.

The MSTN gene is located on the long (q) arm of chromosome 2 at position 32.2.

More precisely, the MSTN gene is located from base pair 190,055,699 to base pair 190,062,728 on chromosome 2.

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

Where can I find additional information about MSTN?

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

  • GDF8
  • GDF-8
  • GDF8_HUMAN
  • growth differentiation factor 8

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 MSTN?

atrophy ; differentiation ; gene ; growth factor ; hypertrophy ; mutation ; protein ; tissue ; wasting

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

See also Understanding Medical Terminology.

References (6 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: December 2008
Published: July 7, 2014