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Reviewed May 2013
What is the official name of the MEGF8 gene?
The official name of this gene is “multiple EGF-like-domains 8.”
MEGF8 is the gene's official symbol. The MEGF8 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 MEGF8 gene?
The MEGF8 gene provides instructions for making a protein whose function is unclear. Based on its structure, the Megf8 protein may be involved in cell processes such as attaching cells to one another (cell adhesion) and helping proteins interact with each other. Researchers also suspect that the Megf8 protein plays a role in the normal shaping (patterning) of many parts of the body during embryonic development.
How are changes in the MEGF8 gene related to health conditions?
Where is the MEGF8 gene located?
Cytogenetic Location: 19q12
Molecular Location on chromosome 19: base pairs 42,325,608 to 42,378,768
The MEGF8 gene is located on the long (q) arm of chromosome 19 at position 12.
More precisely, the MEGF8 gene is located from base pair 42,325,608 to base pair 42,378,768 on chromosome 19.
See How do geneticists indicate the location of a gene? in the Handbook.
Where can I find additional information about MEGF8?
You may also be interested in these resources, which are designed for genetics professionals and researchers.
What other names do people use for the MEGF8 gene or gene products?
See How are genetic conditions and genes named? in the Handbook.
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 MEGF8?
You may find definitions for these and many other terms in the Genetics Home Reference Glossary.
See also Understanding Medical Terminology.
References (5 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.