MAGT1 Back

magnesium transporter 1

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NCBI Description of MAGT1

This gene encodes a magnesium cation transporter protein that localizes to the cell membrane. This protein also associates with N-oligosaccharyl transferase and therefore may have a role in N-glycosylation. Mutations in this gene cause mental retardation X-linked type 95 (MRX95). This gene may have multiple in-frame translation initiation sites, one of which would encode a shorter protein with an N-terminus containing a signal peptide at amino acids 1-29.

Community Annotation of MAGT1 Add / Edit MAGT1: 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

MAGT1 is highly significantly mutated in
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MAGT1 is significantly mutated in
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MAGT1 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 MAGT1