Candidate gene
Candidate Gene is a term used in genetic research to refer to a gene whose location is associated with a particular phenotype or trait. The identification of candidate genes is a crucial step in the study of genetics and genomics, and it plays a significant role in the understanding of genetic diseases and genetic disorders.
Definition[edit | edit source]
A candidate gene is a gene that is suspected of being involved in a particular genetic trait, phenotype, or disease based on its location or biological function. This suspicion is usually based on previous genetic linkage studies that have identified a region of the genome associated with the trait or disease.
Identification[edit | edit source]
The identification of candidate genes is a complex process that involves several steps. First, a genome-wide association study (GWAS) is conducted to identify regions of the genome that are associated with the trait or disease. Once these regions have been identified, researchers then look for genes within these regions that have a known or suspected function related to the trait or disease. These genes become the "candidates" for further study.
Role in Genetic Research[edit | edit source]
Candidate genes play a crucial role in genetic research. They provide a starting point for understanding the genetic basis of diseases and traits. By studying candidate genes, researchers can gain insights into the biological processes that underlie these conditions and potentially develop new treatments or interventions.
Limitations[edit | edit source]
While the candidate gene approach has been successful in identifying genes associated with many traits and diseases, it has limitations. One major limitation is that it relies on existing knowledge about gene function, which is incomplete. Additionally, the candidate gene approach can be time-consuming and expensive, as it often involves extensive genetic testing and analysis.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD