SLC6A19 Back

solute carrier family 6 (neutral amino acid transporter), member 19

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NCBI Description of SLC6A19

This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder.

Community Annotation of SLC6A19 Add / Edit SLC6A19: 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).


SLC6A19 is highly significantly mutated in
SLC6A19 is significantly mutated in
SLC6A19 is near significance in

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

Data details

Mutation list for SLC6A19