SLC2A1 Back

solute carrier family 2 (facilitated glucose transporter), member 1

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NCBI Description of SLC2A1
This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia.

Community Annotation of SLC2A1 Add / Edit SLC2A1: 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

SLC2A1 is highly significantly mutated in
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SLC2A1 is significantly mutated in
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SLC2A1 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 SLC2A1