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NCBI Description of MYNN

This gene encodes a member of the BTB/POZ and zinc finger domain-containing protein family that are involved in the control of gene expression. Alternative splicing results in multiple transcript variants and a pseudogene has been identified on chromosome 14.

Community Annotation of MYNN Add / Edit MYNN: Annotations

No community annotations yet for MYNN.
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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).


MYNN is highly significantly mutated in
MYNN is significantly mutated in
MYNN is near significance in

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

Data details

Mutation list for MYNN