NIPA2 Back

non imprinted in Prader-Willi/Angelman syndrome 2

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NCBI Description of NIPA2
This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.

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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

NIPA2 is highly significantly mutated in
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NIPA2 is significantly mutated in
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NIPA2 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 NIPA2