GPD1L Back

glycerol-3-phosphate dehydrogenase 1-like

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NCBI Description of GPD1L

The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS).

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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).


GPD1L is highly significantly mutated in
GPD1L is significantly mutated in
GPD1L is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for GPD1L