APOD Back

apolipoprotein D

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NCBI Description of APOD
This gene encodes a component of high density lipoprotein that has no marked similarity to other apolipoprotein sequences. It has a high degree of homology to plasma retinol-binding protein and other members of the alpha 2 microglobulin protein superfamily of carrier proteins, also known as lipocalins. This glycoprotein is closely associated with the enzyme lecithin:cholesterol acyltransferase - an enzyme involved in lipoprotein metabolism.

Community Annotation of APOD Add / Edit APOD: Annotations

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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

APOD is highly significantly mutated in
(none)
APOD is significantly mutated in
(none)
APOD is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for APOD