SLC39A13 Back

solute carrier family 39 (zinc transporter), member 13

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NCBI Description of SLC39A13

This gene encodes a member of the LIV-1 subfamily of the ZIP transporter family. The encoded transmembrane protein functions as a zinc transporter. Mutations in this gene have been associated with the spondylocheiro dysplastic form of Ehlers-Danlos syndrome.

Community Annotation of SLC39A13 Add / Edit SLC39A13: 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).


SLC39A13 is highly significantly mutated in
SLC39A13 is significantly mutated in
SLC39A13 is near significance in

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

Data details

Mutation list for SLC39A13