USP9X Back

ubiquitin specific peptidase 9, X-linked

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NCBI Description of USP9X
This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

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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

USP9X is highly significantly mutated in
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USP9X is significantly mutated in
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USP9X 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 USP9X