SLC26A9 Back

solute carrier family 26, member 9

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NCBI Description of SLC26A9
This gene is one 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 yet have markedly different tissue expression patterns. The product of this gene is a highly selective chloride ion channel regulated by WNK kinases. Alternative splicing results in multiple transcript variants encoding differing isoforms.

Community Annotation of SLC26A9 Add / Edit SLC26A9: Annotations

No community annotations yet for SLC26A9.
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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

SLC26A9 is highly significantly mutated in
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SLC26A9 is significantly mutated in
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SLC26A9 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 SLC26A9