SLC22A3 Back

solute carrier family 22 (extraneuronal monoamine transporter), member 3

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NCBI Description of SLC22A3

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein.

Community Annotation of SLC22A3 Add / Edit SLC22A3: Annotations

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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).


SLC22A3 is highly significantly mutated in
SLC22A3 is significantly mutated in
SLC22A3 is near significance in

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

Data details

Mutation list for SLC22A3