SLC38A8 Back

solute carrier family 38, member 8

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of SLC38A8

Community Annotation of SLC38A8 Add / Edit SLC38A8: Annotations

No community annotations yet for SLC38A8.
Sort mutations by: Tumor type  Mutation type  Position  
Straightedge cursor Expand

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

SLC38A8 is highly significantly mutated in
SLC38A8 is significantly mutated in
SLC38A8 is near significance in
combined cohort
PanCan
39 patients (0%)

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

Data details


• Mutation list for SLC38A8