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
COMP

COMP

Reviewed February 2008

What is the official name of the COMP gene?

The official name of this gene is “cartilage oligomeric matrix protein.”

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

The COMP gene provides the instructions for making the COMP protein. This protein is found in the extracellular matrix, which is an intricate lattice of proteins and other molecules that forms in the spaces between cells. Specifically, the COMP protein is located in the extracellular matrix surrounding the cells that make up ligaments and tendons, and near cartilage-forming cells (chondrocytes). Chondrocytes play an important role in bone formation (osteogenesis). In the bones of the spine, hips, and limbs, the process of osteogenesis starts with the formation of cartilage, which is then converted into bone.

The normal function of the COMP protein is not fully known. It is believed to play a role in cell growth and division (proliferation) and the self-destruction of cells (apoptosis), as well as in the regulation of cell movement and attachment. Research has also shown that the COMP protein binds strongly to calcium.

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

multiple epiphyseal dysplasia - caused by mutations in the COMP gene

More than 20 mutations in the COMP gene that cause dominant multiple epiphyseal dysplasia have been identified. This disorder can also be caused by mutations in four other genes; however, the majority of individuals have mutations in the COMP gene.

Mutations in the COMP gene that cause dominant multiple epiphyseal dysplasia change one protein building block (amino acid) or result in small additions or deletions of amino acids in the COMP protein. All identified mutations have occurred in two regions of the COMP protein, which are referred to as the type III and C-terminal domains. COMP mutations lead to the improper folding of the COMP protein in the endoplasmic reticulum, a structure in the cell involved in protein processing and transport. The abnormal COMP protein is unable to leave the endoplasmic reticulum, which causes this cellular structure to enlarge. The endoplasmic reticulum eventually becomes so large that it is no longer able to function normally, and the chondrocyte dies. The premature death of chondrocytes results in diminished growth of the long bones and short stature.

Researchers believe that the lack of COMP protein in the spaces between the chondrocytes leads to the formation of abnormal cartilage. This abnormal cartilage probably breaks down easily, which results in early-onset osteoarthritis.

pseudoachondroplasia - caused by mutations in the COMP gene

About 60 mutations in the COMP gene have been identified in individuals with pseudoachondroplasia. One particular mutation is found in approximately 30 percent of affected individuals. This mutation results in the deletion of a single amino acid, called aspartic acid, in the COMP protein. This gene mutation is usually written as 469delD or D469del. Most other COMP gene mutations involve the substitution of one amino acid for another amino acid in the COMP protein.

Mutations in the COMP gene that cause pseudoachondroplasia also result in the buildup of COMP protein in the endoplasmic reticulum and eventual chondrocyte death. It is not clear why some mutations in the COMP gene cause pseudoachondroplasia and other mutations cause dominant multiple epiphyseal dysplasia.

Where is the COMP gene located?

Cytogenetic Location: 19p13.1

Molecular Location on chromosome 19: base pairs 18,782,772 to 18,791,304

The COMP gene is located on the short (p) arm of chromosome 19 at position 13.1.

The COMP gene is located on the short (p) arm of chromosome 19 at position 13.1.

More precisely, the COMP gene is located from base pair 18,782,772 to base pair 18,791,304 on chromosome 19.

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

Where can I find additional information about COMP?

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

  • cartilage oligomeric matrix protein (pseudoachondroplasia, epiphyseal dysplasia 1, multiple)
  • COMP_HUMAN
  • EDM1
  • EPD1
  • MED
  • PSACH
  • pseudoachondroplasia (epiphyseal dysplasia 1, multiple)
  • THBS5
  • thrombospondin-5

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 COMP?

acids ; amino acid ; apoptosis ; aspartic acid ; bone formation ; calcium ; cartilage ; cell ; chondrocyte ; deletion ; dysplasia ; endoplasmic reticulum ; extracellular ; extracellular matrix ; gene ; mutation ; osteogenesis ; proliferation ; protein ; short stature ; stature ; substitution

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

See also Understanding Medical Terminology.

References (9 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: February 2008
Published: October 27, 2014