SLC26A1 Back

solute carrier family 26 (sulfate transporter), member 1

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NCBI Description of SLC26A1

This gene is a member of a family of sulfate/anion transporter genes. Family members are well conserved in their genomic (number and size of exons) and protein (aa length among species) structures, but have markedly different tissue expression patterns. This gene is primarily expressed in the liver, pancreas, and brain. Three splice variants that encode different isoforms have been identified.

Community Annotation of SLC26A1 Add / Edit SLC26A1: 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).


SLC26A1 is highly significantly mutated in
SLC26A1 is significantly mutated in
SLC26A1 is near significance in

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

Data details

Mutation list for SLC26A1