DLX6: Difference between revisions
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Latest revision as of 08:19, 17 March 2025
DLX6 is a gene that provides instructions for making a protein that plays a crucial role in the development of the nervous system. This gene is part of a larger family of genes known as the distal-less (DLX) family, which are involved in the formation and development of various tissues and organs during embryonic development.
Function[edit]
The DLX6 gene is involved in the development of the nervous system, particularly the brain. It is expressed in specific regions of the brain, including the forebrain and the basal ganglia, which are involved in movement, learning, and memory. The protein produced by the DLX6 gene acts as a transcription factor, which means it attaches (binds) to specific regions of DNA and helps control the activity of certain other genes.
Clinical significance[edit]
Mutations in the DLX6 gene have been associated with various neurological disorders. For example, some studies have suggested a link between DLX6 mutations and conditions such as autism and schizophrenia, although more research is needed to confirm these findings.
See also[edit]
References[edit]
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External links[edit]
- DLX6 at the National Center for Biotechnology Information


