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SLC16A12


Official Full Name
solute carrier family 16 member 12
Organism
Homo sapiens
Gene ID
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

Cat.No. Product Name Price
SHH408588 shRNA set against Human SLC16A12 (NM_213606.3) Inquiry
SHH408592 shRNA set against Mouse SLC16A12 (NM_172838.3) Inquiry
SHR229530 shRNA set against Mouse Slc16a12(NM_172838.3) Inquiry
Cat.No. Product Name Price
MiUTR1M-10758 SLC16A12 miRNA 3'UTR clone Inquiry
MiUTR4H-TG08171 SLC16A12 miRNA 3'UTR clone Inquiry
CDCB191719 Rabbit SLC16A12 ORF clone (XM_002718378.2) Inquiry
CDCH080964 human SLC16A12 ORF clone (NM_213606.3) Inquiry
CDCH400620 Rat SLC16A12 ORF clone(NM_001191637.1) Inquiry
CDCR271747 Mouse Slc16a12 ORF Clone(NM_172838.3) Inquiry
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