This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. Two transcript variants encoding the same protein have been found for this gene.
A synthesized peptide derived from human APOL3, corresponding to a region within N-terminal amino acids.
A synthesized peptide derived from human APOL4, corresponding to a region within C-terminal amino acids.
A synthesized peptide derived from human APOL5, corresponding to a region within C-terminal amino acids.
A synthesized peptide derived from human APOL6, corresponding to a region within N-terminal amino acids.
This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. Widely expressed; highly expressed in the uterus, fetal brain and spinal cord, also detected in heart, liver, lung, colon, spleen, thymus, prostate, placenta, adrenal gland, salivary and mammary gland.
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