background:
APOL6 is a member of the apolipoprotein L gene family. It is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles.
Function:
May affect the movement of lipids in the cytoplasm or allow the binding of lipids to organelles.
Subcellular Location:
Cytoplasm (Probable).
Tissue Specificity:
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.
Similarity:
Belongs to the apolipoprotein L family.
Database links:
UniProtKB/Swiss-Prot: Q9BWW8.1
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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