Has glycerol-3-phosphate dehydrogenase activity
Homodimer
Expressed in liver (at protein level)
An autosomal recessive disorder characterized by onset of moderate to severe transient hypertriglyceridemia in infancy that normalizes with age. The hypertriglyceridemia is associated with hepatomegaly, moderately elevated transaminases, persistent fatty liver, and the development of hepatic fibrosis.
No mutation information available.
Genes with an experimentally identified or computationally predicted synthetic-lethal relationship to GPD1, aggregated across our SSL data sources. Click any partner node to view that gene’s page.
Nodes and edges are coloured by the SSL data source. Partners appearing in more than one source are shown in grey.
No clinical trials information available.