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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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Creatine transporter 2; CRT2; MCT 12; monocarboxylate transporter; Monocarboxylate transporter 12; monocarboxylic acid transporter 12; MOT12; 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
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