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.
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Protein Aliases: Creatine transporter 2; CRT2; MCT 12; Monocarboxylate transporter 12; monocarboxylic acid transporter 12; Solute carrier family 16 member 12; solute carrier family 16, member 12 (monocarboxylic acid transporter 12)
Gene Aliases: CJMG; CRT2; MCT12; SLC16A12
UniProt ID: (Human) Q6ZSM3
Entrez Gene ID: (Human) 387700
Molecular Function: transporter