Apolipoprotein D

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Apolipoprotein D
Protein APOD PDB 2APD.png
Rendering based on PDB 2APD.
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
Symbol APOD
External IDs OMIM107740 MGI88056 HomoloGene1246 GeneCards: APOD Gene
RNA expression pattern
PBB GE APOD 201525 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 347 11815
Ensembl ENSG00000189058 ENSMUSG00000022548
UniProt P05090 P51910
RefSeq (mRNA) NM_001647 NM_001301353
RefSeq (protein) NP_001638 NP_001288282
Location (UCSC) Chr 3:
195.57 – 195.58 Mb
Chr 16:
31.3 – 31.31 Mb
PubMed search [1] [2]

Apolipoprotein D is a protein that in humans is encoded by the APOD gene.[1][2][3] Unlike other lipoproteins, which are mainly produced in the liver, apolipoprotein D is mainly produced in the brain and testes.[4]

Function

Apolipoprotein D (Apo-D) is 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. It is a glycoprotein of estimated molecular weight 33 KDa. Apo-D is closely associated with the enzyme lecithin:cholesterol acyltransferase - an enzyme involved in lipoprotein metabolism.[3]ApoD has also been shown to be an important link in the transient interaction between HDL and LDL particles and between HDL particles and cells.[5]

Clinical significance

APOD is a biomarker of androgen insensitivity syndrome (AIS). APOD is an androgen up-regulated gene in normal scrotal fibroblast cells in comparison to CAIS labia majora cells.[6]

APOD is associated with neurological disorders and nerve injury, especially related to myelin sheath. APOD was shown to be elevated in a rat model of stroke.[4] APOD is elevated in patients with schizophrenia, bipolar disorder, and Alzheimer's disease.[4]

References

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Further reading

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External links

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