The protein encoded by this gene is a member of the apolipoprotein C1 family. This gene is expressed primarily in the liver, and it is activated when monocytes differentiate into macrophages. A pseudogene of this gene is located 4 kb downstream in the same orientation, on the same chromosome. This gene is mapped to chromosome 19, where it resides within a apolipoprotein gene cluster. Alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined.
A synthesized peptide derived from human APOC2, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human APOC3, corresponding to a region within the internal amino acids.
A synthetic peptide from human APOC3
A synthesized peptide derived from human APOC4, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human APOD, corresponding to a region within the internal amino acids.
Apolipoprotein D (ApoD) is a member of the lipocalin superfamily of ligand transporters,and has been implicated in the transport of small hydrophobic molecules. ApoD is also a component of plasma high-density lipoproteins (HDL). Alteration of ApoD expression has been linked to multiple neurological disorders,including Alzheimer's disease.
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