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Overview
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Background
EGLN3 (Egl-9 Family Hypoxia Inducible Factor 3) is a Protein Coding gene. Diseases associated with EGLN3 include Hypoxia and Erythrocytosis, Familial, 2, Autosomal Recessive. Among its related pathways are ErbB signaling pathway and Cellular Senescence (REACTOME). Gene Ontology (GO) annotations related to this gene include oxidoreductase activity and oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen. An important paralog of this gene is EGLN1.
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