NDN Back

necdin homolog (mouse)

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NCBI Description of NDN
This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons.

Community Annotation of NDN Add / Edit NDN: Annotations

No community annotations yet for NDN.
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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

NDN is highly significantly mutated in
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NDN is significantly mutated in
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NDN 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 NDN