ALX1 Back

ALX homeobox 1

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NCBI Description of ALX1
The specific function of this gene has yet to be determined in humans; however, in rodents, it is necessary for survival of the forebrain mesenchyme and may also be involved in development of the cervix. Mutations in the mouse gene lead to neural tube defects such as acrania and meroanencephaly.

Community Annotation of ALX1 Add / Edit ALX1: 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

ALX1 is highly significantly mutated in
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ALX1 is significantly mutated in
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ALX1 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 ALX1