Your search for "slc16a12" returned 261 TaqMan® SNP Genotyping Assays
solute carrier family 16 member 12
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]
Please enter the information below and press OK to send your cart to Core Services for purchase.