FAM9B Back

family with sequence similarity 9, member B

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NCBI Description of FAM9B
This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be localized to the nucleus as the protein contains several nuclear localization signals, and has similarity to a synaptonemal complex protein.

Community Annotation of FAM9B Add / Edit FAM9B: Annotations

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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

FAM9B is highly significantly mutated in
(none)
FAM9B is significantly mutated in
(none)
FAM9B is near significance in
(none)

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

Data details


• Mutation list for FAM9B