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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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Protein Aliases: Glycerol-3-phosphate dehydrogenase 1-like protein; GPD1-L
Gene Aliases: 2210409H23Rik; D9Ertd660e; GPD1-L; GPD1L; KIAA0089
UniProt ID: (Human) Q8N335, (Mouse) Q3ULJ0
Entrez Gene ID: (Human) 23171, (Mouse) 333433
Molecular Function:
dehydrogenase
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