SLC17A8 Back

solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8

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NCBI Description of SLC17A8

This gene encodes a vesicular glutamate transporter. The encoded protein transports the neurotransmitter glutamate into synaptic vesicles before it is released into the synaptic cleft. Mutations in this gene are the cause of autosomal-dominant nonsyndromic type 25 deafness. Alternate splicing results in multiple transcript variants.

Community Annotation of SLC17A8 Add / Edit SLC17A8: 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).


Legend

SLC17A8 is highly significantly mutated in
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SLC17A8 is significantly mutated in
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SLC17A8 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 SLC17A8