FAM20A Back

family with sequence similarity 20, member A

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NCBI Description of FAM20A
This locus encodes a protein that is likely secreted and may function in hematopoiesis. A mutation at this locus has been associated with amelogenesis imperfecta and gingival hyperplasia syndrome. Alternatively spliced transcript variants have been identified.

Community Annotation of FAM20A Add / Edit FAM20A: Annotations

No community annotations yet for FAM20A.
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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

FAM20A is highly significantly mutated in
(none)
FAM20A is significantly mutated in
(none)
FAM20A is near significance in
(none)

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

Data details


• Mutation list for FAM20A