SLC22A9

SLC22A9 is a gene that encodes a protein in the human body. This protein is part of the solute carrier family 22, member 9 (organic anion transporter), also known as SLC22A9. The SLC22A9 gene is located on chromosome 11 in humans.

Function

The SLC22A9 gene is responsible for encoding a protein that is part of the solute carrier family. This family of proteins is involved in the transport of various substances across the cell membrane. Specifically, the protein encoded by the SLC22A9 gene is an organic anion transporter, which means it helps move negatively charged molecules, or anions, across the cell membrane.

Clinical Significance

Mutations in the SLC22A9 gene can lead to various health conditions. For example, some studies have suggested a link between variations in this gene and susceptibility to gout, a type of inflammatory arthritis. However, more research is needed to fully understand the role of SLC22A9 in human health and disease.

Research

Research into the SLC22A9 gene and its encoded protein is ongoing. Scientists are particularly interested in understanding how variations in this gene may contribute to disease susceptibility and drug response. This research could potentially lead to new treatments for diseases such as gout and other conditions related to organic anion transport.

File:SLC22A9 gene location on human chromosome 11.png

SLC22A9 gene location on human chromosome 11

See Also

• Solute carrier family
• Organic anion transporter
• Gout

References

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