Exome

Last updated on: 04.09.2024

Dieser Artikel auf Deutsch

Requires free registration (medical professionals only)

Please login to access all articles, images, and functions.

Our content is available exclusively to medical professionals. If you have already registered, please login. If you haven't, you can register for free (medical professionals only).


Requires free registration (medical professionals only)

Please complete your registration to access all articles and images.

To gain access, you must complete your registration. You either haven't confirmed your e-mail address or we still need proof that you are a member of the medical profession.

Finish your registration now

DefinitionThis section has been translated automatically.

In genetics, the exome refers to the entirety of an organism's exons, i.e. all sections that potentially code for proteins. In humans, it comprises around 23,000 genes with approximately 50 million DNA bases.

General informationThis section has been translated automatically.

The exome cannot be mapped to the transcriptome, as not all potential protein-coding genes are actually active and a gene can be processed in several different RNA patterns (splice variants).

For medical diagnostics, it has proven useful to sequence only the exome, which comprises around 1-2% of the human genome, rather than the entire genome. However, 89% of the known disease-causing variants are found here. In genetic diagnostics, all genes of these coding sections are sequenced simultaneously.

Last updated on: 04.09.2024