Solute carrier family 16 member 12 is a protein that in humans is encoded by the SLC16A12 gene.
[5]
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].
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