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SLC16A12

Official Full Name
solute carrier family 16 member 12
Organism
Homo sapiens
GeneID
387700
Background
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]
Synonyms
CJMG; CRT2; MCT12; CTRCT47;

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