FAM126A Back

family with sequence similarity 126, member A

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NCBI Description of FAM126A

The protein encoded by this gene may play a part in the beta-catenin/Lef signaling pathway. Expression of this gene is down-regulated by beta-catenin. Defects in this gene are a cause of hypomyelination with congenital cataract (HCC).

Community Annotation of FAM126A Add / Edit FAM126A: Annotations

No community annotations yet for FAM126A.
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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).


FAM126A is highly significantly mutated in
FAM126A is significantly mutated in
FAM126A is near significance in

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

Data details

Mutation list for FAM126A