MEOX2 Back

mesenchyme homeobox 2

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NCBI Description of MEOX2

This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.

Community Annotation of MEOX2 Add / Edit MEOX2: 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).


MEOX2 is highly significantly mutated in
MEOX2 is significantly mutated in
MEOX2 is near significance in

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

Data details

Mutation list for MEOX2