KRT12 Back

keratin 12 (Meesmann corneal dystrophy)

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NCBI Description of KRT12
KRT12 encodes the type I intermediate filament chain keratin 12, expressed in corneal epithelia. Mutations in this gene lead to Meesmann corneal dystrophy.

Community Annotation of KRT12 Add / Edit KRT12: Annotations

No community annotations yet for KRT12.
Sort mutations by: Tumor type  Mutation type  Position  
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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

KRT12 is highly significantly mutated in
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KRT12 is significantly mutated in
(none)
KRT12 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 KRT12