SLC16A12( Human )
solute carrier family 16 member 12
Alias
CJMG|CRT2|CTRCT47|MCT12
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].