• Source: Solute carrier family 16 member 12
    • Solute carrier family 16 member 12 is a protein that in humans is encoded by the SLC16A12 gene.


      Function


      This gene encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria. [provided by RefSeq, Mar 2010].


      References




      Further reading



      This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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