In this article, we are going to explore
SLC22A14 in a deep and detailed way, analyzing different aspects, points of view and perspectives related to this topic. We will delve into its origin, evolution, impact on society and possible future implications. Additionally, we will examine different expert opinions and relevant studies that shed light on
SLC22A14 and its relevance today. This article seeks to offer a complete and enriching view on
SLC22A14, with the aim of providing our readers with a deep and global understanding of this topic that is of interest to a wide audience.
Solute carrier family 22 member 14 is a protein that in humans is encoded by the SLC22A14 gene.[5]
Function
This gene encodes a member of the organic-cation transporter family. It is located in a gene cluster with another member of the family, organic cation transporter like 3. The encoded protein is a transmembrane protein which is thought to transport small molecules and since this protein is conserved among several species, it is suggested to have a fundamental role in mammalian systems. Alternative splicing results in multiple transcript variants. .
References
Further reading
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
