ZNF423: Difference between revisions

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Revision as of 06:52, 11 February 2025

ZNF423 is a gene that encodes a zinc finger protein and plays a crucial role in various biological processes. It is located on chromosome 16 in humans and is expressed in many tissues, including the brain, heart, and kidney.

Function

The ZNF423 gene encodes a protein that functions as a transcription factor, which means it helps control the activity of other genes. This protein contains several zinc finger domains, which are regions that allow it to bind to specific sequences of DNA. By binding to these sequences, the ZNF423 protein can regulate the expression of other genes, influencing various cellular processes.

Clinical Significance

Mutations in the ZNF423 gene have been associated with several medical conditions. For example, some studies have found that variations in this gene may increase the risk of developing breast cancer. Other research has suggested that mutations in ZNF423 may be involved in the development of nephronophthisis, a type of kidney disease that can lead to kidney failure.

Research

Research on the ZNF423 gene is ongoing, with scientists seeking to better understand its functions and the effects of its mutations. This research could potentially lead to new treatments for diseases associated with this gene.

See Also

References

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