DIAPH3 Back

diaphanous homolog 3 (Drosophila)

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NCBI Description of DIAPH3
This gene encodes a member of the diaphanous subfamily of the formin family. Members of this family are involved in actin remodeling and regulate cell movement and adhesion. Mutations in this gene are associated with autosomal dominant auditory neuropathy 1. Multiple transcript variants encoding different isoforms have been found for this gene.

Community Annotation of DIAPH3 Add / Edit DIAPH3: Annotations

No community annotations yet for DIAPH3.
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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

DIAPH3 is highly significantly mutated in
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DIAPH3 is significantly mutated in
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DIAPH3 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 DIAPH3