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APOA2

Apolipoprotein A-II is a protein that in humans is encoded by the APOA2 gene.[1]

Function

Function

This gene encodes apolipoprotein (apo-) A-II, which 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. Defects in this gene may result in apolipoprotein A-II deficiency or hypercholesterolemia.[2]

Interactions

Interactions

APOA2 has been shown to interact with PLTP.[3]

Interactive pathway map

Interactive pathway map

Click on genes, proteins and metabolites below to link to respective articles. [§ 1]

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<imagemap> Image:StatinPathway_WP430.png
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Statin Pathway edit
  1. The interactive pathway map can be edited at WikiPathways: “Statin_Pathway_WP430”.
References

References

  1. Tsao YK, Wei CF, Robberson DL, Gotto AM, Chan L (Dec 1985). “Isolation and characterization of the human apolipoprotein A-II gene. Electron microscopic analysis of RNA:DNA hybrids, nucleotide sequence, identification of a polymorphic MspI site, and general structural organization of apolipoprotein genes”. The Journal of Biological Chemistry. 260 (28): 15222–31. PMID 2415515.
  2. “Entrez Gene: APOA2 apolipoprotein A-II”.
  3. Pussinen PJ, Jauhiainen M, Metso J, Pyle LE, Marcel YL, Fidge NH, Ehnholm C (Jan 1998). “Binding of phospholipid transfer protein (PLTP) to apolipoproteins A-I and A-II: location of a PLTP binding domain in the amino terminal region of apoA-I”. Journal of Lipid Research. 39 (1): 152–61. PMID 9469594.
External links
Further reading

Further reading

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