FKBP14 Back

FK506 binding protein 14, 22 kDa

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NCBI Description of FKBP14
The protein encoded by this gene is a member of the FK506-binding protein family of peptidyl-prolyl cis-trans isomerases. The encoded protein is found in the lumen of the endoplasmic reticulum, where it is thought to accelerate protein folding. Defects in this gene are a cause of a type of Ehlers-Danlos syndrome (EDS). Both a protein-coding variant and noncoding variants are transcribed from this gene.

Community Annotation of FKBP14 Add / Edit FKBP14: Annotations

No community annotations yet for FKBP14.
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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

FKBP14 is highly significantly mutated in
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FKBP14 is significantly mutated in
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FKBP14 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 FKBP14