Apolipoprotein A-II
Protein-coding gene in the species Homo sapiens
From Wikipedia, the free encyclopedia
Apolipoprotein A-II is a protein that in humans is encoded by the APOA2 gene.[5] It is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotein D. ApoA-II regulates many steps in HDL metabolism, and its role in coronary heart disease is unclear.[6] Defects in this gene may result in apolipoprotein A-II deficiency or hypercholesterolemia.[7]
External IDsOMIM: 107670; MGI: 88050; HomoloGene: 1242; GeneCards: APOA2; OMA:APOA2 - orthologs
Interactions
ApoA-II has been shown to interact with phospholipid transfer protein.[8]
Interactive pathway map
Click on genes, proteins and metabolites below to link to respective articles.[§ 1]
Statin pathway edit
- The interactive pathway map can be edited at WikiPathways: "Statin_Pathway_WP430".
