SLC23A2 Back

solute carrier family 23 (nucleobase transporters), member 2

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NCBI Description of SLC23A2
The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two required transporters and the encoded protein accounts for tissue-specific uptake of vitamin C. Previously, this gene had an official symbol of SLC23A1.

Community Annotation of SLC23A2 Add / Edit SLC23A2: Annotations

No community annotations yet for SLC23A2.
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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).


Legend

SLC23A2 is highly significantly mutated in
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SLC23A2 is significantly mutated in
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SLC23A2 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for SLC23A2