SLC16A12

SLC16A12

Target · Creatine transporter

SLC16A12 Solute carrier family 16 member 12 · Monocarboxylate transporter 12

SLC16A12, also known as MCT12 or CRT2, is a plasma membrane transporter that moves creatine and its precursor guanidinoacetate across the cell membrane. It belongs to the solute carrier family 16 and the major facilitator superfamily. Browse Assay Genie's current range of SLC16A12 research reagents below, or read on for the biology behind the target.

Basolateral cell membraneCreatine transporterLinked to juvenile cataract
516 aa
Protein length
~56 kDa
Molecular weight
10q23.31
Gene locus
MFS transporter
Protein family
Target information

What is SLC16A12 (solute carrier family 16 member 12)?

SLC16A12 functions as a transporter for creatine and for its precursor, guanidinoacetate (GAA). Transport of both substrates is independent of resting membrane potential and of extracellular Na(+), Cl(-) or pH. The protein contributes to creatine biosynthesis and to the distribution of creatine between cells and tissues.

The SLC16A12 gene encodes a transmembrane protein that is found at the cell membrane, including the basolateral cell membrane. It belongs to the major facilitator superfamily and to the monocarboxylate porter family (TC 2.A.1.13), and HGNC places it in the solute carrier family 16 gene group. The NCBI Gene summary notes that it likely plays a role in monocarboxylic acid transport. Mouse and rat both carry an ortholog named Slc16a12.

The protein is known as monocarboxylate transporter 12 (MCT12) and as CRT2. Earlier HGNC names described it as a member of the solute carrier family 16 of monocarboxylic acid transporters. A mutation in the SLC16A12 gene has been associated with juvenile cataracts with microcornea and renal glucosuria, which makes the transporter of interest for studies of creatine handling, lens biology and renal transport.

Creatine metabolism

SLC16A12 transports creatine and guanidinoacetate and contributes to creatine biosynthesis and distribution, making it relevant to studies of how creatine is moved between cells.

Membrane transport biology

As a basolateral member of the monocarboxylate porter family, it is used to study substrate transport that does not depend on membrane potential, Na(+), Cl(-) or pH.

Cataract and eye research

A mutation in the SLC16A12 gene is associated with juvenile cataracts with microcornea, linking the transporter to studies of lens and corneal development.

Renal glucosuria studies

The same gene mutation has been associated with renal glucosuria, so SLC16A12 is relevant to research on kidney transport and its disruption in disease.

Background

SLC16A12 frequently asked questions

What does SLC16A12 do?

SLC16A12 is a transporter for creatine and its precursor guanidinoacetate. Transport of both is independent of resting membrane potential and of extracellular Na(+), Cl(-) or pH. It contributes to creatine biosynthesis and distribution. Check the datasheet of any product for its validated reactivity.

What other names does SLC16A12 go by?

SLC16A12 is also called MCT12 (monocarboxylate transporter 12) and CRT2. Its HGNC name is solute carrier family 16 member 12. Older names describe it as a member of the solute carrier family 16 of monocarboxylic acid transporters.

Is SLC16A12 linked to disease or conserved in other species?

A mutation in the SLC16A12 gene has been associated with juvenile cataracts with microcornea and renal glucosuria. Orthologs exist in mouse and rat, where the gene is named Slc16a12, so rodent systems can be used to study its function.

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Related targets

Other solute carrier family 16 monocarboxylate transporters and related SLC transporters with products at Assay Genie.

Gene and protein annotations from HGNC, NCBI Gene and UniProt Q6ZSM3; product specifications from Assay Genie datasheets.

SLC16A12 Product listing

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