FAM83H Back

family with sequence similarity 83, member H

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NCBI Description of FAM83H
The protein encoded by this gene plays an important role in the structural development and calcification of tooth enamel. Defects in this gene are a cause of amelogenesis imperfecta type 3 (AI3).

Community Annotation of FAM83H Add / Edit FAM83H: Annotations

No community annotations yet for FAM83H.
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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

FAM83H is highly significantly mutated in
(none)
FAM83H is significantly mutated in
(none)
FAM83H is near significance in
(none)

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

Data details


• Mutation list for FAM83H