SLC16A12 Back

solute carrier family 16, member 12 (monocarboxylic acid transporter 12)

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NCBI Description of SLC16A12

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.

Community Annotation of SLC16A12 Add / Edit SLC16A12: Annotations

No community annotations yet for SLC16A12.
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Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


SLC16A12 is highly significantly mutated in
SLC16A12 is significantly mutated in
SLC16A12 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for SLC16A12