CNTN4 Back

contactin 4

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NCBI Description of CNTN4

This gene encodes a member of the contactin family of immunoglobulins. Contactins are axon-associated cell adhesion molecules that function in neuronal network formation and plasticity. The encoded protein is a glycosylphosphatidylinositol-anchored neuronal membrane protein that may play a role in the formation of axon connections in the developing nervous system. Deletion or mutation of this gene may play a role in 3p deletion syndrome and autism spectrum disorders. Alternative splicing results in multiple transcript variants.

Community Annotation of CNTN4 Add / Edit CNTN4: 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

CNTN4 is highly significantly mutated in
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CNTN4 is significantly mutated in
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CNTN4 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 CNTN4