SLC1A3 Back

solute carrier family 1 (glial high affinity glutamate transporter), member 3

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NCBI Description of SLC1A3

This gene encodes a member of a member of a high affinity glutamate transporter family. Mutations in this gene are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.

Community Annotation of SLC1A3 Add / Edit SLC1A3: 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).


SLC1A3 is highly significantly mutated in
SLC1A3 is significantly mutated in
14 patients (5%)
SLC1A3 is near significance in

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

Data details

Mutation list for SLC1A3