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

No community annotations yet for SLC6A19.
Sort mutations by: Tumor type  Mutation type  Position  
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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

SLC6A19 is highly significantly mutated in
(none)
SLC6A19 is significantly mutated in
(none)
SLC6A19 is near significance in
(none)

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

Data details


• Mutation list for SLC6A19